Dec 052025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

DWP and Treasury silent over mystery of £2 billion cuts to disability benefits 1

Unacceptable’ new figures show rejections of Access to Work claims have shot up this year 3

Watchdog’s silence after removing figures that showed social security spending is not ‘spiralling’ 5

Manifesto calls on next Welsh government to enable disabled people to ‘flourish and thrive’ 7

Deaf people who use BSL face ‘entrenched’ health and social care exclusion, say government advisers 9

Years of scapegoating rhetoric has led to ‘envy and resentment’ of those with blue badges, research finds 11

Other disability-related stories covered by mainstream media this week 14

 

 

DWP and Treasury silent over mystery of £2 billion cuts to disability benefits

The government has refused to explain the impact that last week’s budget will have on disabled people who receive benefits, despite repeated requests for clarity over cuts of up to £580 million a year.

The Department for Work and Pensions (DWP) and the Treasury have both failed to provide any details of the cuts to spending on disability benefits of nearly £2 billion over five years.

It is just DWP’s latest failure of transparency since Labour’s new minister for social security and disability, Sir Stephen Timms, promised to improve its openness to public scrutiny in September 2024.

Treasury documents published on the day of last week’s budget showed that, from next April, the government will increase DWP’s “capacity” to carry out reassessments of disabled people’s capacity for work through the work capability assessment (WCA).

DWP will also carry out more face-to-face assessments, which have been drastically cut back since the early weeks of the pandemic, both through WCAs and assessments of eligibility for personal independence payment (PIP).

The Treasury’s budget costings document also said DWP would be “changing the frequency” of reviews of PIP awards, which would allow it to “complete award reviews on time, reducing the number of people who are called to a PIP assessment when their function has not changed, and allowing providers to redirect resource to WCA re-assessments”.

The budget document described this measure as “extending Personal Independence Payment award reviews periods”.

The budget costings document said these changes will “ensure people receive the right health or disability benefit and the system is sustainable”.

But there are significant question-marks over these measures, because the changes together are set to save the government £85 million next year, £310 million in 2027-28, £520 million in 2028-29, £580 million in 2029-30 and £455 million in 2030-31, a total of £1.95 billion over five years.

Disability News Service (DNS) has been asking the Treasury and DWP to clarify how these cuts will be made for more than a week.

The Treasury initially claimed that the budget documents were not announcing new policies, but were “just costing existing plans from planned welfare reforms – so nothing new from this”.

But neither department has been able to point to where or when these “existing plans” were announced by DWP, particularly the changes in reviews of PIP awards, and how these changes will affect PIP recipients and those on out-of-work disability benefits.

Although the government has previously made it clear that it wanted to increase reassessments through the WCA, and to increase the number of face-to-face WCAs and PIP assessments, these ideas were included in March’s green paper.

Green papers are supposed to lay out policy proposals for consultation, but they are not announcements of final decisions on government policy.

DNS has been unable to find any DWP announcements on these and the other measures in last week’s budget documents since the spring budget on 26 March 2025, other than a brief reference to carrying out more PIP face-to-face assessments in a speech by the then work and pensions secretary Liz Kendall in May.

Both DWP and the Treasury have refused to provide clarity on the budget changes, with DWP instead releasing a statement that failed to explain what measures it was taking on PIP award reviews*.

It is the latest in a string of DWP failures on transparency since Labour came to power, continuing years of similar failings under successive Conservative-led governments.

At Labour’s annual conference in Liverpool, in September 2024, Sir Stephen told DNS: “The department has absurdly refused to answer lots of the questions that you have asked and that is something that we want to change… because public scrutiny is a good thing, and it puts pressure on ministers and on civil servants to have the consequences of what they are doing known about publicly.”

Meanwhile, DWP’s controversial new anti-fraud bill – now to be known as the Public Authorities (Fraud, Error, and Recovery) Act – has become law after receiving royal assent on Tuesday.

Last month, cross-party MPs warned that ministers’ refusal to introduce a key protection into the bill could see a repeat of the countless deaths caused by the austerity measures of past governments.

And they warned that future “authoritarian” governments could misuse the powers the Labour government has claimed through the bill, which applies to England, Scotland and Wales.

One of those powers will allow DWP to force banks to examine the accounts of claimants of means-tested benefits and then provide details of any accounts where there have been potential breaches of benefit eligibility rules.

Disability Rights UK said it was “deeply concerned” at the “bank spying bill” becoming law.

It said on X/Twitter: “A government agency that is notorious for punitive sanctions and bureaucratic faults that have cost lives, this will have dire consequences.”

*The statement is included here as a footnote, as it failed to answer the questions put to the department by DNS: “We are increasing the number of face-to-face assessments and tackling the backlog of Work Capability Assessments we inherited, by changing the frequency of PIP assessment reviews. This will ensure claimants receive the right level of support while at the same time reducing unnecessary award reviews, as we shift our focus from welfare to work, skills and opportunities.”

4 December 2025

 

 

Unacceptable’ new figures show rejections of Access to Work claims have shot up this year

Ministers have been forced to admit that the proportion of Access to Work claims they are rejecting has leapt by more than a fifth this year, with disabled campaigners describing the figures as “unacceptable” and “clearly worrying”.

The figures, provided through a response to a written parliamentary question, show the proportion of applications rejected has risen by more than 22 per cent in 2025-26 so far, compared with 2024-25.

This follows a rise of more than 12 per cent in 2024-25, Labour’s first year in control of the Department for Work and Pensions (DWP)*.

It is the strongest evidence yet to support concerns being raised by disabled campaigners, who have been warning for months that Access to Work (AtW) support is being cut.

The figures came just days after Disability News Service (DNS) reported that DWP was claiming that “an issue” with data was preventing it releasing detailed monthly figures on AtW claims.

The new figures were released by Sir Stephen Timms, the minister for social security and disability, in response to a question from Labour’s former shadow minister for disabled people, Vicky Foxcroft.

Rather than requesting more detailed monthly data, as DNS had done, she had asked for the number and proportion of AtW claims that had been closed in each year since 2022-23.

In 2022-23, Sir Stephen told her, 31,482 applications were not approved, which was 30 per cent of all decisions.

The proportion of applications rejected fell to 24 per cent in 2023-24, the last full year of the Conservative government, but then last year under the new Labour government – which claims it is trying to increase the number of disabled people in work – it rose to 27 per cent of all applications being rejected (a 12.5 per cent increase).

And so far this year (April to October), the proportion of claims rejected has increased even more sharply, with 27,297 applications not approved, one in three (33 per cent) of all decisions, a rise of more than 22 per cent (six percentage points) on 2024-25.

Although he provided these figures, Sir Stephen failed to provide Foxcroft with data showing the frequency of reasons for rejections (which include “no contact from the applicant”, “insufficient evidence provided”, “applicant not eligible” and “application not pursued”.

Disabled consultant, broadcaster and campaigner Shani Dhanda, co-founder of the Access to Work Collective, said the increase in claims being rejected was “unacceptable”.

But she also called again for clarity from ministers on exactly what was happening within the AtW system.

She told DNS: “We still have no idea where people are being lost in the system, and the vague reasons given tell us nothing about what actually went wrong.

What we see on the ground is chaos: phone calls going unanswered, people cut off mid-call, evidence repeatedly misplaced, and applicants waiting so long for approvals, change of circumstances or renewals, that work opportunities disappear.

The fact that non-approvals have jumped to 33 per cent, the highest in recent years, while transparency has been stripped back, is unacceptable.

Access to Work is meant to support disabled workers, not shut them out.”

David Buxton, chief executive of the disabled people’s organisation Action on Disability, which in October produced evidence showing the average AtW support hours of disabled people it had been working with had plunged from 22.5 to just four in two-and-a-half years, said the new figures were “clearly worrying”.

And he criticised the department for the lack of transparency over what was driving the increased rejections.

He said: “Without clear data, we are all being left to guess, but what’s absolutely clear is that disabled people need a system that works.

We must push for workable, sustainable and effective solutions that genuinely support people to stay in work.”

He added: “The numbers point to a system that is struggling to meet disabled people’s needs.

When more than 100,000 applications over recent years have not been approved, and when a third of decisions this year are non-approvals, that has a very real impact on people’s ability to stay in work or take up new roles.”

Catherine Eadie, a social enterprise founder and Access to Work claimant, and a member of the Access to Work Collective, added: “For those of us dealing with Access to Work daily, these figures match what we see: procedural errors, misinterpretation of guidance, misplaced evidence, and delays so long that people’s jobs and businesses become unviable while they wait.

When approval rates drop this sharply and explanations get vaguer, trust is impossible.”

Foxcroft told DNS: “I encourage ministerial colleagues to investigate this concerning increase in the number of cases being rejected by the DWP and ensure that it feeds into their wider work on reform of the current programme.”

She said: “It has long been clear that Access to Work is not fit for purpose. 

I am pleased that ministers have acknowledged this and begun to take action through the Pathways to Work green paper.

These statistics show, however, that there is still a long way to go towards removing the workplace barriers disabled people face every day.”

DWP is expected to announce its proposals for AtW reform in the next few weeks.

*It took control in July 2024, so the first three months of 2024-25 were under Conservative control

4 December 2025

 

 

Watchdog’s silence after removing figures that showed social security spending is not ‘spiralling’

The government’s “independent” spending watchdog has refused to explain why it removed figures from its crucial budget forecast report that proved spending on social security is not spiralling out of control.

The move by the Office for Budget Responsibility (OBR) will help the government – and commentators – justify expected future cuts to spending, such as to personal independence payment and out-of-work disability benefits.

This week, the Sunday Times reported that the government was set to push ahead with plans, first proposed in March’s Pathways to Work green paper, to prevent disabled young people under the age of 22 from receiving the health element of universal credit.

And in a speech in London on Monday, the prime minister, Sir Keir Starmer, said that the social security system had “trapped people in poverty”, particularly young disabled people.

Her said young disabled people were being “simply written off” and trapped “in a cycle of worklessness and dependency for decades” which “costs the country money” and was “bad for our productivity”.

Disability News Service and academics, other journalists and disabled activists have been using the OBR figures since early this year to dismantle claims that “welfare spending” is increasing at an unmanageable rate.

But these crucial figures have been omitted from OBR’s latest Economic and Fiscal Outlook report, which was published last week alongside the budget.

The figures were first highlighted by a disabled activist in February, after they were included in the OBR’s October 2024 Economic and Fiscal Outlook.

The October 2024 figures showed that the share of GDP* taken by social security spending was stable, and was even predicted to fall from 11.1 per cent to 11.0 per cent in 2027-28 and 2028-29, before rising slightly back to 11.1 per cent in 2029-30.

Updated figures were included in an OBR report in March this year**, and they showed that social security spending was predicted to be even lower – as a proportion of GDP – than previously predicted.

The figures were included in one of the charts released alongside the Economic and Fiscal Outlook report, which is published alongside every budget.

That chart (chart 5.2) tracked “welfare spending” as a proportion of GDP for every year back to 2010-11, when it was 12 per cent of GDP.

But last week’s version of chart 5.2 was substantially different.

Instead of showing how spending has changed year by year since 2010-11 as a proportion of GDP, table 5.2 now shows how the proportion of government spending in different areas has changed relative to 2010-11 levels, making it impossible to compare social security spending levels year-by-year and prove that it has not “spiralled”.

What last week’s OBR report does show (see table 5.1 in the main report) is that the chancellor’s spending decisions – including scrapping the two-child benefit cap – have not led to an increase in the proportion of GDP being spent on social security, compared with previous predictions.

The figures show that welfare spending for 2024-25 was significantly lower than predicted last year (10.8 per cent compared with a predicted 11.1 per cent) as a proportion of GDP, while the predicted spending for this year is also lower than was forecast by the OBR last year (10.9 per cent versus 11.1 per cent), while the forecast levels for the next four years have remained unchanged.

These figures show that any attempt by media, civil servants and politicians – such as chancellor Rachel Reeves last year, DWP in January, and opposition MPs such as Tory leader Kemi Badenoch in September – to make false claims that social security spending is spiralling out of control would be misleading, if not deeply dishonest.

This week, OBR’s press office refused three times to even acknowledge emails asking why it had removed the historic figures from the report.

The Treasury had also not commented by noon today (Thursday) on whether it requested OBR to remove the historic welfare spending figures.

OBR’s refusal to comment came in a week that its chair, Richard Hughes, resigned after the watchdog mistakenly published its outlook report before Reeves had delivered her budget speech to MPs.

*Gross domestic product, the size of the country’s economy in a particular year

**Chapter five of OBR’s Economic and Fiscal Outlook – March 2025, chart 5.2, shows welfare spending as a percentage of GDP: https://obr.uk/efo/economic-and-fiscal-outlook-march-2025/

4 December 2025

 

 

Manifesto calls on next Welsh government to enable disabled people to ‘flourish and thrive’

The national body for disabled people’s organisations (DPOs) in Wales has issued five major demands to political parties ahead of next spring’s elections to the Welsh Senedd.

The Disabled People’s Manifesto, published by Disability Wales, includes a call for the UN Convention on the Rights of Persons with Disabilities (UNCRPD) to be incorporated into Welsh law.

It also demands a “robust” disabled people’s rights plan – which should include the appointment of a minister for disabled people – ahead of the current Welsh government’s 10-year plan, which is likely to be published this month.

And it calls for Welsh politicians to champion disabled people’s leadership – supporting disabled leaders in public life, and ensuring they are represented in decision-making and policy development – and for government to fund the work of DPOs.

The manifesto demands a guaranteed right to independent living, with reforms to social care, health and housing that focus on dignity, choice, and accessibility, and for the new government to promote inclusion, and end the institutionalisation of disabled people.

And it calls for the social security system to be devolved from the UK to the Welsh government, as has been – partially – achieved in Scotland.

The manifesto, From Barely Surviving to Truly Thriving, has been developed with DPOs from across Wales and individual disabled people.

In all, more than 250 disabled people helped shape the manifesto, which outlines demands from politicians over the four years from the May 2026 elections.

Although the Welsh Labour government included a pledge to incorporate UNCRPD into Welsh law in its programme for government in 2021, Disability Wales says no progress has been made towards this goal, and so the convention remains “a guiding framework rather than a legally enforceable standard”.

A draft version of the Welsh government’s Disabled People’s Rights Plan, when it was published in May, saw the government accused of putting up a “smokescreen” with a document that lacked “teeth” and was full of pledges to carry out reviews and produce guidance while offering no new money.

The 61-page plan included no significant promises on key areas such as social care, accessible housing and transport, and disability poverty, and was short of concrete targets.

Disability Wales says in its manifesto that the draft plan “must be strengthened to ensure long-term impact and accountability”, while there must be “sustained investment and infrastructure” for DPOs so they can be “essential partners” in delivering the plan.

Disability Wales also says in its manifesto that disabled people “remain underrepresented in political and public life”.

It calls for all political parties to publish the percentage of their representatives who identify as disabled people and their targets for improving these figures in the run-up to the 2026 Senedd and 2027 local government elections.

The manifesto says that barriers to independent living “strip away autonomy and keep people trapped in unsuitable housing, inflexible care arrangements and discriminatory environments”, and it calls instead for accessible housing, inclusive health services, and an end to institutional care.

It also calls for a national campaign to tackle the “ableism, stigma, and discrimination” faced by disabled people.

Devolving social security systems to Wales would enable “more responsive, fair, and inclusive support systems, designed in coproduction with disabled people and DPOs”, the manifesto says.

It concludes: “Disabled people in Wales deserve more than mere survival.

We deserve the right to truly flourish and thrive.

We know that change is possible, but it requires commitment, collaboration and courage.

We call on all political parties to adopt these five calls and work with us to build a Wales where disabled people are not just supported but celebrated.”

Disability Wales has also launched a “commitment form”, asking every political party and candidate to state clearly and publicly where they stand on each of the manifesto’s five calls.

Their responses will be updated during the Senedd election campaign and used afterwards to monitor delivery and implementation of the policy demands.

Rhian Davies, chief executive of Disability Wales (DW), said: “DW’s vision is for an inclusive, equitable and barrier free society.

Disabled people in Wales deserve more than mere survival; we deserve the right to truly flourish and thrive.

Following the recent module two Covid-19 Inquiry report, which criticised government failure to appreciate the level of risk faced by disabled people, resulting in escalating death rates and a reversal of rights, this manifesto is a call to action for all political parties to commit to real change.

Together, we can move from surviving to thriving.”

Natalie Jarvis, DW’s policy and research officer, said: “As someone involved in the co-production of this manifesto alongside DPOs and the voices of hundreds of disabled people across Wales, I have heard stories of exhaustion, frustration and injustice but also of hope, resilience and vision.

Disabled people know exactly what needs to change.

What we need now is the political will to act and for parties to commit to our calls within their own manifestos ahead of the elections.”

4 December 2025

 

 

Deaf people who use BSL face ‘entrenched’ health and social care exclusion, say government advisers

Deaf people who use British Sign Language (BSL) face “entrenched” and “systemic” exclusion from health and social care services across Britain, according to a new report by government advisers.

The report* found that Deaf and Deafblind people’s lack of access to services costs the Treasury millions of pounds through “unmet needs, wasted appointments and delays in care”. 

Better access to health and social care services would allow more Deaf and Deafblind people to find work and progress in their careers, and contribute more through taxation, says the report.

The report focuses on the experiences of Deaf and Deafblind BSL-users in England, Scotland and Wales, and is based on a review of their access to services carried out by the government’s BSL Advisory Board’s health and social care sub-group.

The report found a “deep-rooted lack of trust” within Deaf and Deafblind communities following repeated experiences of exclusion from services, which often left them “traumatised” by a lack of access to health and social care.

One Deaf woman spent five months sleeping in an accident and emergency cubicle because there was no bed available in mental health services that had BSL support.

Repeated access failures and exclusions often cause “accumulated trauma” over a person’s lifetime, says the report.

BSL users usually need “high levels of motivation, perseverance with inaccessible systems and patience with the inexperience of professionals trying to meet their needs” if they want to access services, the report found.

Many BSL-users avoid social care and health services completely due to their past experiences because they believe their communication needs will not be met. 

There are believed to be about 87,000 Deaf BSL-users in the UK, and 25,000 people who use BSL as their main language.

The report makes a string of recommendations to the UK and devolved governments, including calls to establish national, 24/7 video relay services for England and Wales; set up national BSL complaints services within England, Scotland and Wales; provide mandatory deaf, deafblind and BSL awareness training for all NHS and social care staff; and address “language deprivation” in deaf children through “early and comprehensive” BSL provision and support for families.

The Locked Out report* follows the passing of the British Sign Language (BSL) Act in April 2022, which was introduced as a private members’ bill by Labour MP Rosie Cooper and recognised BSL as a language of England, Wales, and Scotland.

The act provided Deaf people with no new rights, but it secured significant support from the Deaf community, and it led the following year to the government setting up its BSL Advisory Board to offer advice to ministers on key issues affecting the Deaf community.

All the board’s members are deaf or deafblind, or have deaf parents or a deaf child.

Craig Crowley, the board’s co-chair, says in a foreword to the report that the document is a “powerful call to action and a roadmap towards a more inclusive and equitable future for BSL users within our health and social care systems”.

He says: “We acknowledge the distressing reality of delayed diagnoses, inadequate treatment, and the emotional impact of communication breakdowns, but we strongly believe these are challenges we can, and must, overcome.”

The British Deaf Association (BDA) welcomed the new report and its “stark” findings, describing it as the “most comprehensive examination ever undertaken into the barriers faced by Deaf and Deafblind BSL users across the NHS and social care systems”.

It said the persistent failures in communication access were causing avoidable harm, entrenched inequalities, and the denial of basic rights for tens of thousands of Deaf and Deafblind people across the UK.

Rebecca Mansell, BDA’s chief executive, said: “This is a ground-breaking report that lays bare the challenges that deaf signers face every day with the NHS and care system. 

This report confirms what Deaf and Deafblind people have been telling government for decades: the health and social care system is not built with our communities in mind. 

We are particularly delighted to see the strong focus in the report’s recommendations on the steps that governments must take to address language deprivation in deaf children and adults.

We strongly endorse the recommendation that governments provide free BSL courses for the families of deaf children. 

This recommendation backs up the recently published report, The Value of British Sign Language – An Economic Analysis, written by Rand Europe, the policy research organisation.

This reports that the teaching of BSL to young deaf children and their families delivers an impressive economic return on investment – up to £14 for every £1 invested. 

This report requires a strong and supportive government response, and we will be contacting BDA members to urge them to write to their MPs.” 

The Department of Health and Social Care had failed to comment on the report by noon today (Thursday).

*Locked out: Exclusion of deaf and deafblind BSL users from health and social care in the UK

4 December 2025

 

 

Years of scapegoating rhetoric has led to ‘envy and resentment’ of those with blue badges, research finds

Years of scapegoating rhetoric and politicians casting disabled people as “scroungers” have reinforced prejudices about the blue badge parking scheme and led to “envy and resentment” instead of equal access, according to a four-year research project.

Half-hearted implementation of the scheme has left disabled people who rely on it feeling worried, angry and frustrated, and like “second-class citizens”, because of the encounters they have had while trying to use their badges, the research concludes.

The research was carried out by Vera Kubenz, a disabled postgraduate researcher at the University of Birmingham, and herself a blue badge holder.

She said this week that she feared that recent rhetoric around disabled people receiving “free cars” through the Motability scheme, and the need for cuts to disability benefits, would lead to a fresh wave of such aggressive and hateful encounters.

In a summary report based on her research, Disabled People’s Encounters with Strangers in Accessible Parking Spaces, Kubenz concludes that, as long as there is wider societal prejudice, hostility and suspicion aimed at disabled people, “there can be no such thing as a truly accessible space”.

As part of her research, she surveyed more than 300 disabled people with experience of encounters – good and bad – while using their blue badges.

In the survey, 74 per cent of disabled people said they had been accused of “faking” their impairments while using their blue badges.

These types of encounters were particularly common for younger disabled people, with some told they were “too young” to be disabled.

One of those who took part in the survey, who is 49, said: “A member of the public stopped me as I was parking in a Blue Badge space.

He knocked on my window, I wound it down and he told me I shouldn’t be parking there, and I had no right to be there.

I explained I was disabled. He said I was too young and there was nothing wrong with me.

I proceeded to get into my wheelchair and get out of the car, in fairness, he did look quite embarrassed when I got out of the car.”

The impact of such encounters was clear, with 91 per cent of disabled people who took part in the survey saying they worried about them, with 40 per cent always worrying and 35 per cent worrying a lot, while more than two thirds (68 per cent) said they sometimes did not use their vehicles because of the worry.

Another survey participant said: “A man in his 50s came over trying to take our car keys out of the car (luckily it was a keyless ignition Motability vehicle).

When he realised he couldn’t get the key he came round to my side trying to grab my Blue Badge.

We was called every name under the sun. The c word, the n word, lots of f yous.

All because we had parked in the disabled bay… I was that upset with the whole incident I wanted to just leave and not have my operation.”

Common locations for encounters were supermarket carparks (87 per cent of those surveyed), near shops (70 per cent) and at hospitals or GP surgeries (58 per cent).

Most people (70 per cent) experienced encounters between a few times a year and a few times a month.

People with chronic illness, who were neurodivergent, or who had mental health conditions were particularly likely to be confronted over their use of accessible parking spaces.

Many of those surveyed said that being under constant suspicion meant they always felt on edge and worried that an encounter could happen at any moment.

Two thirds (67 per cent) of disabled people taking part in the survey had experienced hate and harassment in accessible parking spaces.

Negative encounters could involve staring, tutting, or hushed comments, while nearly half (46 per cent) of people had been insulted and a third (32 per cent) had been threatened, while some (six per cent) had been subjected to physical violence.

But most people (69 per cent) had also had at least one positive encounter, often a positive chat with another blue badge holder.

Kubenz says in the report that enforcement of blue badge spaces is often a postcode lottery.

Although some of those surveyed said their councils took action to enforce rules around the use of blue badges, many others said their council took no action.

One said: “I wish that Blue Badge parking was properly policed because what we have now is the worst of both worlds, people making assumptions and not looking at the badge and trying to police it for the benefit of those who do, but in doing so make lots of assumptions.”

Ultimately, says Kubenz, all disabled people who use blue badges risk confrontations because “nobody can live up to the impossible stereotype required for being truly ‘deserving’”.

The survey of 304 blue badge holders was carried out in 2023, while there were 20 follow-up interviews; it was open to holders of blue badges who had had at least one encounter, were over 18, and lived in England.

Kubenz told Disability News Service this week: “I am very concerned that the renewed government and media statements about disabled people’s ‘free cars’ and cuts to both in- and out-of-work benefits will intensify the resentment non-disabled people have against all disabled people, and that this will lead to more encounters because people feel entitled to ‘police’ blue badge bays because they are seen as a perk rather than essential for access.

These confrontations can range from underhanded comments to intrusive questions, verbal abuse, and even physical violence.

I fear the current government rhetoric will directly contribute to more aggression and hate towards disabled people.”

She added: “Many of the people interviewed had little faith that the government would change anything about blue badge policy or awareness, precisely because they are responsible for so many of the misconceptions that lead to encounters.

I conclude in my research that currently the blue badge scheme only provides bare minimum access; it is not about equality, but about keeping disabled people ‘in their place’.”

On Friday 12 December, between 12pm and 1pm, Kubenz is hosting a webinar on the findings of her Politics of Parking project, with guest speakers Anjna Patel, a trustee of Disabled Motoring UK, and accessible transport campaigner Christiane Link

4 December 2025

 

 

Other disability-related stories covered by mainstream media this week

Health secretary Wes Streeting is launching an independent review into rising demand for mental health, ADHD, and autism services in England. It will look at whether there is evidence of over-diagnosis and what gaps in support exist. Reports of the review first emerged in October: https://www.bbc.co.uk/news/articles/ce8q26q2r75o

Labour proposed while in opposition how to introduce assisted suicide via a private members’ bill, suggesting that this would still allow “heavy influence” for the government in the process, a leaked document has revealed. The document proposed a change strikingly similar to the private members’ bill put forward eventually by Labour MP Kim Leadbeater. The leak raises fresh questions over how much government control there has been behind her bill: https://www.theguardian.com/society/2025/dec/03/labour-planned-in-opposition-introduce-assisted-dying-via-private-members-bill

Virgin Media has been fined £23.8 million for putting thousands of “vulnerable” people “at risk of harm” when switching them from an analogue to a digital landline. Media watchdog Ofcom found the company failed to protect people who relied on telecare alarms to call for help, after Virgin Media self-reported a number of “serious incidents” in November and December 2023: https://www.theguardian.com/media/2025/dec/01/virgin-media-fined-vulnerable-customers-landline-ofcom

4 December 2025

 

News provided by John Pring at www.disabilitynewsservice.com

 

Nov 182025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

A vector graphic with an arm holding a wine-coloured megaphone. A spikey speech bubble points to the microphone and says, in all caps, "protest the budget"

 

Saturday 29th November

1pm @ Swansea Castle

With Disabled People Against Cuts Cymru (DPAC Cymru) and others.

No disability cuts.

Hands of Motability.

Living wages.

Pension justice.

Rent control.

Trade union rights.

No to hate & division.

Make the rich pay.

 

The budget is being written by the Swansea West MP.

A photo of a mobile billboard featuring the face of the Torsten Bell MP. Text, in black on yellow, says: "Swansea West: £4,500 disability cuts backed by your MP." Text, in white on black says "11,592 disabled people here rely on that support. Torsten Bell supports these cuts. Protest disability support." At the bottom-right is the Amnesty International logo, which is black on yellow.

Disabled people defeated his Spring Statement & PIP disability cuts. Now he’s back with another anti-working-class budget. We will defeat him again.

First Bus workers are on strike over low pay.

65 student nurses have been told there are no vacancies when they graduate.

£25 million of job cuts at Swansea University.

Disabled people are still fighting cuts and Swansea women are still fighting for pension justice.

Politicians try to divide us by blaming migrants, low-paid workers, trans people & disabled people.

“An injury to one is an injury to all”

 

We want to co-organise a protest with everyone affected by the budget.

Contact Disabled People Against Cuts Cymru (DPAC Cymru)

Swansea – Protest the budget (PDF for printing)

A graphic of the DPAC Cymru logo. There is the main DPAC logo to the left, which is a red, pink, blue, and green circle being held by four hands of different skin tones, with the words "disabled people against cuts" surrounding it, and an upside-down black traingle in the middle bearing the letters D P A C. On the right is the word Cymru (pronounced cum ree) (C Y M R U) in large letters, and the background of the letters are cutouts of the Welsh flag. Above Cymru (pronounced cum ree) is written the words Disabled People Against Cuts. Below Cymru (pronounced cum ree) are the words Rights, not charity, and the equivilant phrase translated into the Welsh language.

This is a graphic advertising a protest in Swansea on the 29th November.

There are striped green and red corners with the text "Swansea" along the diagonal.

A speech bubble that says "protest the budget" is exiting a megaphone.

There are three clasped hands of different skin tones and the text "an injury to one is an injury to all" curves around them.

Large text says "Saturday 29th November. 1pm at Swansea Castle, S A 1, 1 D W." Smaller text says "With Disabled People Against Cuts (D P A C) and others."

Beneath, with a ripped paper effect, is text that says "no disability cuts. Hands off motability. Living wages. Pension justice. Rent control. Trade union rights. No to hate & division. Make the rich pay."

This is a graphic advertising a protest in Swansea on the 29th November.

There are striped green and red corners with the text "Swansea" and "Protest" along the diagonals, and the text "budget" in the center.

Beneath, in all-caps, is the text "Sat. 29 November. 1pm @ Swansea Castle."

In the centre of the leaflet is text that starts in bold with "The budget is being written by the Swansea West MP."

The text continues: "Disabled people defeated his Spring Statement & PIP disability cuts. Now he’s back with another anti-working-class budget. We will defeat him again."

There are then five bullet points that say: "First Bus workers are on strike over low pay. 65 student nurses have been told there are no vacancies when they graduate. £25 million of job cuts at Swansea University. Disabled people are still fighting cuts and Swansea women are still fighting for pension justice. Politicians try to divide us by blaming migrants, low-paid workers, trans people & disabled people."

At the bottom, with a ripped paper effect and a pink background, is the D P A C Cymru logo - a red, green, blue and pink wheel being held by four hands of different skin tones. To the right is a blue box that asks "Your org's logo here?" and text that says "We want to co-organise a protest with everyone affected by the budget", the email D P A C dot C Y M R U at gmail.com and the website "D P A C hyphen C Y M R U dot C A R R D dot C O."
Nov 072025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

New official figures expose how politicians and media have repeatedly lied about social security spending 1

Ministers listen to disabled campaigners and return key accessibility duty to railways bill 3

Government review calls for ‘safer, more supportive’ workplaces for disabled people 7

DWP refuses to rule out cuts to PIP next year 10

Safeguarding probe launched after veteran disabled activist reports ‘terrifying’ care home experience 12

Tens of thousands tell government: We reject any plans to cut PIP 14

Other disability-related stories covered by mainstream media this week 16

 

 

New official figures expose how politicians and media have repeatedly lied about social security spending

New official figures – hidden by government and opposition parties – have exposed months of lies by politicians and the media about “spiralling” spending on social security and the need to cut benefits.

The updated statistics from the Office for Budget Responsibility (OBR) show that, rather than “spiralling out of control”, social security spending is predicted to be lower in 2029-30 than it is this year.

Previous figures published by OBR in October 2024 showed that the share of GDP* taken by social security spending was stable, and even predicted to fall from 11.1 per cent to 11.0 per cent in 2027-28 and 2028-29, before rising slightly back to 11.1 per cent in 2029-30.

Despite those figures, it appears to have become an accepted fact across the mainstream media – and particularly right-wing publications – that social security spending is out of control.

But the new OBR figures**, published in March this year but apparently not reported on by the media, show predicted spending to be even lower than previously forecast.

They show that social security spending is predicted to be 10.9 per cent of GDP this year, then 11 per cent in 2026-27, 10.8 per cent in 2027-28, 10.7 in 2028-29 and 10.8 per cent in 2029-30, when it will be 0.2 percentage points lower than next year’s expected level.

The figures – which may be adjusted again later this month by OBR – highlight the repeated dishonesty of politicians and media commentators who insist that chancellor Rachel Reeves must act in this month’s budget to curb what they claim is rapidly-rising spending on social security.

Although spending on personal independence payment (PIP) has been rising quickly, and is predicted to rise further – likely due to the combined impact of the pandemic on long-term health, the rise in mental ill-health, lengthy NHS waiting-lists after 15 years of austerity, greater awareness of PIP, the rising state pension age, and the cost-of-living crisis – the OBR figures show overall social security spending to be stable and even predicted to fall slightly.

This week, Disability News Service (DNS) approached the Treasury, the Department for Work and Pensions (DWP), the Conservative party, the Labour party and Reform UK, asking why they have repeatedly stated that social security spending was spiralling and needed to be cut when it was now set to fall over the next few years.

By noon today (Thursday), Labour, the Conservatives and Reform UK had all failed to comment on the figures or even acknowledge the approach.

The Treasury passed the questions to DWP.

A response from DWP ignored the questions asked by DNS and so is included as a footnote to this article***.

The last few days have seen Tory leader Kemi Badenoch and Reform UK leader Nigel Farage both calling for cuts to social security spending.

Badenoch said in a speech on Tuesday that she had a plan to “cut welfare”, and “reduce eligibility for lower-level mental health issues”, repeatedly conflated PIP with out-of-work disability benefits, misleadingly claimed that “sickness benefits pay more than the minimum wage”, and attacked the Motability car scheme.

Two months ago, she said the social security system was “out of control”.

Last week, Reform UK’s work and pensions spokesperson Lee Anderson said his party would cut £3.2 billion a year from PIP spending by “fully [removing] those with anxiety disorders, but not serious psychiatric disorders, from PIP eligibility”.

And this week, Reform UK leader Nigel Farage wrongly claimed that the benefits bill had “ballooned” this year, while he also claimed – again wrongly – that the million lowest-paid workers would “all be better off if they claimed to have mild anxiety”.

Chancellor Rachel Reeves was more subtle in her “scene setter” speech ahead of the budget, describing welfare spending on Tuesday misleadingly as one of the “pressures on the public finances”.

Last month, she repeated the false claim that welfare spending was spiralling, telling Channel 4 News: “We can’t get to the end of this parliamentary session and have done nothing, because if more and more of our money that we spend as a government is spent on welfare, you’ve got less for the NHS, you’ve got less for schools.”

Meanwhile, the harm caused by previous efforts to cut spending on disability benefits was highlighted on Tuesday by a protest outside DWP’s Caxton House headquarters by disabled artist, writer and filmmaker Dolly Sen.

Sen – who declared the building a “crime scene” because of the “structural violence built into the welfare system” – was joined by campaigners Joy Dove and Ian Briggs.

One of their aims was to call on the government to “prioritise the safety, dignity and lives of claimants in all welfare policy”.

Dove’s daughter Jodey Whiting died in February 2017, and in June a second inquest into her suicide – following her mother’s eight-year campaign for justice and accountability – found that her “deteriorating” mental health had been “precipitated” by the withdrawal of her out-of-work disability benefits after she missed a work capability assessment.

Briggs has campaigned for justice for five years over his claims that the actions of the Child Maintenance Service – part of DWP – contributed to Gavin’s decision to take his own life.

Sen said: “They call it welfare; I call it warfare.

The DWP wages war on the poor, the disabled, and the already-broken.

It’s a ministry of cruelty that has turned suffering into policy, despair into a spreadsheet.

Behind every tick box is a human being who didn’t survive the paperwork.”

She added: “We will continue to campaign until the state stops treating life as a cost to cut.”

Dove said: “I want to show I am not going away. I want a public inquiry and justice for Jodey, if that’s the last thing I do.

The coroner said the DWP triggered Jodey to kill herself, and I think someone should be held accountable.

I am also doing this for the other families who have lost loved ones due to the DWP.”

*Gross domestic product, the size of the country’s economy in a particular year

**Chapter five of OBR’s Economic and Fiscal Outlook – March 2025, chart 5.2, shows welfare spending as a percentage of GDP: https://obr.uk/efo/economic-and-fiscal-outlook-march-2025/

***A DWP spokesperson said: “We’re shifting our focus from welfare to work, skills, and opportunities, so more people can move out of poverty and into good, secure jobs as part of our Plan for Change. We’re also modernising jobcentres, delivering a youth guarantee, and funding local programmes like Connect to Work so people get the skills to thrive, and businesses get the workforce they need.”

6 November 2025

 

 

Ministers listen to disabled campaigners and return key accessibility duty to railways bill

The government has restored accessibility to the heart of its planned rail reforms, in a victory for disabled campaigners and allies who fought plans to remove a key measure from new legislation.

Labour had previously dropped plans to ensure there was a statutory duty to ensure accessibility was central to all policy decisions made by the new Great British Railways (GBR).

This led to disabled campaigners and allies accusing transport secretary Heidi Alexander of scrapping commitments on accessibility made by the last Conservative government.

But when the government published its new railways bill yesterday (Wednesday), it included a “passenger and accessibility” duty.

In its response to a consultation on the bill, also published yesterday, the Department for Transport (DfT) said it would “include a passenger and accessibility duty in primary legislation to ensure GBR factors in the needs and interests of disabled passengers when carrying out its statutory functions”.

It said it was taking this step “in line with the feedback and strong support outlined in responses to the consultation”.

The bill says that GBR, ministers and the regulator must all “exercise their functions” in “the manner best calculated to promote the interests of users and potential users of railway passenger services including, in particular, the needs of disabled persons”.

The bill will create GBR, a new publicly-owned company that will bring together management of passenger services and rail infrastructure.

The government also plans to use the bill to introduce a stronger passenger watchdog and simplify fares and tickets.

DfT said this watchdog would have “an explicit role in accessibility by monitoring how services are delivered to disabled passengers and advocating for improvements where issues arise”.

Ministers have also published a new “roadmap to an accessible railway”.

The roadmap – which covers England, Scotland and Wales – promises that GBR “will embed accessibility into the heart of the railway”.

But despite a series of pledges in the roadmap to improve the railway’s accessibility, questions are already being asked about the government’s commitment to funding the cost of transforming the railway’s infrastructure to ensure it is accessible to disabled passengers.

The roadmap says £373 million will be spent over the next five years on the Access for All station improvement programme, but it admits that this will only increase the proportion of rail stations across Britain that are step-free from pavement to platform from 56 per cent to 58 per cent.

But the roadmap also promises that reforms to the Access for All programme will lead to a future commitment to only spend “up to” £70 million a year.

This appears to be a reduction in spending, once inflation is accounted for, as the Department for Transport (DfT) previously allocated £350 million for the scheme from 2019 to 2024, although only £285 million of that was eventually spent over those five years.

Among other measures in the roadmap – and following years of calls from campaigners, particularly the Campaign for Level Boarding – the government promises a “comprehensive study of level boarding to identify and scope practical, cost-effective solutions for achieving level boarding across prioritised locations on the rail network”. 

A strategy next year will include the government’s approach to “improving level boarding and setting out what is needed from trains and infrastructure in the future, to allow people to board with greater ease”.

The roadmap also promises that Network Rail will deliver a plan to improve the reliability and performance of lifts and escalators at stations across the rail network.

And it says improvements will be made over the next 16 months to the much-criticised Passenger Assist – which allows disabled passengers to book assistance in advance of their journey – that will be aimed at making it “more reliable and consistent”.

On customer information on station accessibility, among the improvements planned are the introduction of “virtual 3D walkthroughs” of 250 of the country’s busiest and most complex stations, and improvements to live information on facilities such as lifts, escalators and accessible toilets.

And eligibility for a disabled persons railcard will be expanded to “cover a wider range of disabilities”.

There will also be a new, “comprehensive” disability equality training programme for rail staff, which will be co-produced and delivered in partnership with disabled people and rolled out across the rail network, with the possibility of a new British Standard for “inclusive service”, which will apply to train companies as they are nationalised.

A new National Accessibility Panel will “oversee and advise on nationally significant issues affecting disabled passengers across the UK”, with membership including disabled people and representatives from disabled people’s organisations, as well as the Disabled Persons Transport Advisory Committee and the Mobility and Access Committee for Scotland.

Emily Sullivan, co-founder of the Association of British Commuters, and a disabled researcher in equality and human rights, said: “After eight months of campaigning, it is a real victory to get core duties for accessibility and socioeconomic value back into the plan for Great British Railways.

Our next task is to make sure these duties are even stronger, and that there is a much better, rights-based framework for regulating accessibility.

There is also an urgent need to secure more funding – with slow progress on Access for All and signs of more austerity policies ahead, such as railway destaffing.”

She said the roadmap was “very short-term” but included some “valuable suggestions”, particularly the commitment to develop a new system of accessibility panels, which “could be transformative for disabled people’s representation” if the system was independent, transparent, and engaged with the public, and co-created with disabled people’s organisations.

But she said there were some “serious omissions”, with “no mention whatsoever of equality or rights-based standards, which should be the foundation of everything else”.

And she said it was “appalling” that there was no “mention or aspiration” towards disabled people’s right to “turn up and go” on the rail network.

Sullivan also said it was “hugely concerning” that the private sector Rail Delivery Group would be developing technologies like Passenger Assist until at least 2027, when it “should have been removed from the area of accessibility years ago”.

She said: “It is important to watch this closely in case the focus on pre-booking technologies is being used once again as a way to destaff the network.”

The disabled people’s organisation Transport for All said the railways bill was “a once-in-a-generation opportunity to rebuild Britain’s railways with accessibility for everyone embedded from the ground up”, but that it must lead to “concrete, enforceable change across the rail network”.

It said it would be closely monitoring developments with the bill and GBR’s licence “to ensure that disabled people’s experiences are central in shaping the next era of Britain’s railways”.

Emma Vogelmann, co-chief executive of Transport for All, said: “This bill is a once-in-a-generation opportunity to rebuild Britain’s railways with accessibility for everyone embedded from the ground up.

We welcome the government’s commitment to include disabled passengers in the new passenger interest duty and to give the passenger watchdog a clear role in monitoring accessibility.”

But she added: “These promises must lead to real, measurable improvements for disabled people who rely on rail.

Accessibility for everyone must be a priority for public transport and a defining principle as Great British Railways takes shape.”

A DfT spokesperson told Disability News Service: “We are fully committed to improving accessibility across the network, and the railways bill includes a statutory duty requiring key bodies in the sector to support all passengers, particularly the needs of disabled people.

Alongside the railways bill, today we published an accessibility roadmap, which is a practical plan to deliver real, measurable change and expanded eligibility for the disabled persons railcard.”

Labour’s Ruth Cadbury, who chairs the Commons transport committee, gave a cautious welcome to the roadmap.

The committee’s Access Denied report on transport accessibility argued for a long-term plan with concrete timescales to address the barriers faced by disabled travellers, with the committee later describing the government’s response to its report as lacking “urgency” and disabled campaigners warning that it left the future of disabled people’s right to travel in “grave danger”.

Cadbury said: “We will take a close look at the roadmap and its implementation to ensure that it delivers on this need.”

She welcomed some of the contents of the roadmap but stressed that “funding needs to be equal to the scale of the challenge”.

She said: “We will be looking closely in the future at whether the roadmap’s ambitions transform the experience of getting around on the rails in practice.”

Rail minister Lord [Peter] Hendy described the roadmap as a “turning point” for disabled rail passengers and said it was “a practical plan to deliver real, measurable change, ahead of the establishment of Great British Railways”.

He said: “We know there is more work to do, but the roadmap lays the foundations for a longer-term transformation under GBR, because an accessible railway isn’t just better for disabled people – it’s better for us all, and this is the start of building one together.”

6 November 2025

 

 

Government review calls for ‘safer, more supportive’ workplaces for disabled people

A government review has called for action by employers and ministers to ensure “safer, more supportive, inclusive workplaces” and to address the barriers faced by sick and disabled people in and out of work.

The final report of the Keep Britain Working review focuses on what employers and government can do to address links between ill-health and economic inactivity.

But it almost completely ignores the views of sick and disabled people, and the risks of forcing someone back into work when they are not well enough, particularly when many of the available jobs are “poorly-paid, strenuous and insecure” and likely to make someone unwell again, as Disability Rights UK pointed out this week.

It also appears to suggest that employers should be given more power in deciding when an employee should return to work, with less say given to GPs, through reforms to the “fit note” system.

The report points to an estimated gain of up to £18 billion a year to employers, government, and the wider economy, if the suggested reforms are introduced.

The review says the UK has been “sliding into an economic inactivity crisis driven in large part by ill-health and by barriers to work faced by disabled people” and it lays out a seven-year plan to “radically improve results in managing health and disability in work”.

In contrast to the months and years of targeted attacks by politicians and right-wing media, in which sick and disabled people have been blamed for the country’s economic problems (see separate story), the review places the responsibility for addressing the “crisis” largely on employers.

  1. It says: “Disabled people describe repeatedly having to self-advocate for workplace adjustments, often with anxiety about whether support will be given or withdrawn in future.
  2. As many conditions are dynamic and fluctuating, this becomes a recurring burden.
  3. It also makes changing roles or employers much harder.”

The 10-month review, led by Sir Charlie Mayfield, former chair of John Lewis Partnership and of the British Retail Consortium, was commissioned last year by the government.

The review says the aim is to “re-humanise the workplace, raise standards, improve access to support, and transform the visibility of data”.

The review was told by ill and disabled employees that they “fear disclosing health conditions or disabilities, and are worried about stigma, discrimination, or damage to career prospects”.

Although Sir Charlie emphasises the risk of “disengaging from work and potential support, or relying on welfare as an alternative to work”, almost all his report calls for action by employers and government and mostly avoids blaming sick and disabled people.

In a letter to work and pensions secretary Pat McFadden and business and trade secretary Peter Kyle, Sir Charlie says: “With the right approach, many more people could stay in work, recover faster, and live healthier, more secure lives.”

The review calls for a “fundamental shift from a model where health at work is largely left to the individual and the NHS, to one where it becomes a shared responsibility between employers, employees and health services”.

Among its recommendations, the review calls for significant reform of the fit note, which is issued by healthcare professionals to provide evidence of their advice on a person’s fitness for work.

It suggests that a new employer-funded system would “offer support and advice, early intervention, good case management, and targeted early-stage treatment pathways”, with this eventually “reducing – or even replacing – the need for the current fit note”, a recommendation that may alarm many campaigners concerned at the power this may give employers over unwell employees.

It also calls for the development of “stay in work” and “return to work” plans, faster access to support, and a new certified “healthy working” standard for employers.

Publishing the report, the government announced a list of about 80 employers that have pledged to become part of the “vanguard” of organisations that will be “early adopters” of the new approach to workplace health.

There are already significant concerns being expressed about the report.

As well as concern over the apparent move towards giving employers more power in deciding an employee’s fitness for work, there is likely to be alarm about the report’s failure to discuss those sick and disabled people who cannot work or even move towards work, and the risks of pressuring them to do so.

There is likely to be disquiet among many disabled people that the list of enthusiastic “vanguard” employers includes Capita, Maximus and Unum, all of which have been linked closely to activity by the Department for Work and Pensions that has caused countless deaths of disabled claimants over the last three decades.

Many will also highlight the government’s continuing cuts to disabled people’s Access to Work packages – with more cuts believed likely in the coming months – and its decision to cut the health element for most new claimants of universal credit who cannot work for disability-related reasons, supposedly as an “incentive”, from April 2026.

The new work and pensions secretary, Pat McFadden, is also expected to take action to prevent most sick and disabled people under the age of 22 from accessing the health element of universal credit.

Another potential concern is that there is little or no mention in the report of working with disabled people and DPOs to implement the review’s recommendations.

Instead, the report talks of the need for a “phased approach… working with willing employers and providers to develop and prove what works, before embedding and extending it across the wider economy over the next 3-7 years.”

But McFadden said yesterday in a written statement to MPs that a new “vanguard taskforce”, to be co-chaired by Sir Charlie, will “bring together representatives from business, disabled people, workers representatives and health experts to shape and deliver this work”.

He did not make it clear how many of the report’s recommendations the government accepted, but he said ministers planned to “work with businesses and disabled people to pilot and develop improvements and reform”.

He said the government was “already piloting innovative approaches to the fit note and we are committed to further reform so that it works better for patients, employers and the health system”.

There are only fleeting mentions in the report of the Access to Work scheme – currently plagued by delays and cuts – and its importance to disabled people in finding and maintaining jobs.

And the review is dismissive of Disability Confident, the much-criticised scheme introduced more than a decade ago by Conservative work and pensions secretary Iain Duncan Smith.

It says: “Schemes such as Disability Confident and Access to Work have several positive features and good intent, but we heard regularly across the review that they were not delivering effectively in practice, with Disability Confident lacking accountability and ‘teeth’ and Access to Work facing long delays and delivery challenges.”

McFadden said: “Business is our partner in building a productive workforce – because when businesses retain talent and reduce workplace ill-health, everyone wins.”

Kyle added: “Many more people could remain in work if they receive the right support – and that’s exactly what today’s action is about.

We believe that when people are treated with dignity and care, businesses flourish.”

6 November 2025

 

 

DWP refuses to rule out cuts to PIP next year

The Department for Work and Pensions (DWP) has refused to rule out spending cuts to personal independence payment (PIP) when it completes a year-long review that is being headed by the disability minister.

Misleading reports in right-wing media last week suggested that updated terms of reference for the review showed ministers had ruled out any cuts to PIP spending.

But the terms of reference suggest exactly the opposite: that spending will not be allowed to be higher than the “projections” published by the Office for Budget Responsibility (OBR) but could be lower.

The terms of reference say: “The purpose of the Review is to ensure that PIP is fair and fit for the future rather than to generate proposals for further savings.

However, the sustainability of the system is an important consideration and so the Review will operate within the OBR’s projections for future PIP expenditure, to ensure it is there to support generations to come.”

This second sentence has been added since the original terms of reference were published in June.

The following sentence has also been added to the terms of reference since June: “We want to ensure public money is spent as effectively as possible in supporting disabled people to live independent and fulfilling lives.”

This week, DWP refused to clarify what it meant by these two sentences, and whether the review could lead to cuts to PIP spending.

Instead, a DWP spokesperson said: “We want a welfare state that is there for those who need it and supports people into work, while delivering fairness to the taxpayer.

That’s why we’re launching the Timms Review to make sure PIP is fair and fit for the future.

We’re shifting our focus from welfare to work, skills and opportunities so more people can move out of poverty and into good, secure jobs as part of the Plan for Change.”

Last week, DWP announced the names of the two disabled people – Dr Clenton Farquharson and Sharon Brennanwho will co-chair the review with Sir Stephen Timms, the minister for social security and disability.

Brennan is a former director of policy and external affairs at National Voices, a coalition of English health and social care charities, and a former member of the Disabled Persons Transport Advisory Committee

Farquharson is a consultant, associate director at Think Local Act Personal, and a board member of both Disability Rights UK and the Race Equality Foundation.

DWP has also launched a recruitment process for the 12 members of the PIP review’s steering group.

The majority of the steering group will be disabled people or representatives of disabled people’s organisations.

These positions will be paid, with a daily fee of £300 for up to five days a month until autumn 2026.

As the Benefits and Work website pointed out, this is likely to mean the steering group will have only about 55 days to complete its work.

It also pointed out that steering group members will not need to sign a gagging clause, although they will be expected to “maintain the confidentiality of information shared in confidence”.

There was shock and alarm this summer when DWP imposed a gagging order – which was later removed – on members of its new Independent Disability Advisory Panel.

In a parliamentary written statement, Sir Stephen said the PIP review would be the first time the government had undertaken co-production with disabled people “on this scale”.

But the terms of reference make it clear that final decisions on any changes will be made by Labour’s new work and pensions secretary, Pat McFadden.

Meanwhile, Benefits and Work also highlighted a string of errors, concerning statements and misleading claims made by Reform UK in a press conference last week on the party’s plans to slash PIP and target the Motability scheme.

6 November 2025

 

 

Safeguarding probe launched after veteran disabled activist reports ‘terrifying’ care home experience

A veteran activist, who has spent her life campaigning for disability rights, has called on the government to fix the “rotten to the core” social care system, after experiencing “terrifying” treatment during a short stay in a care home.

Rachel Hurst, now 86, is hoping to give evidence about her experience to Baroness Casey’s social care commission, which has been set up by the government to examine the crisis in adult social care.

For 12 days last month as a temporary resident at Miranda House in Royal Wootton Bassett, she says she was frequently left in wet and soiled pads – sometimes all day – and had to remind staff to bring her the medication she needed to take every morning.

Sheets were not changed, she was left in bed for hours at a time during the day, there was little communication from staff, some of whom were “rude” and uncaring, she says, and the home did not have the hoist needed to allow her to use the toilet safely, while there was no monitoring of her fluid intake.

She said the care provided was “dire”, even though the home itself was clean and her room was mainly well-equipped, and she was left with an infection which she believes was caused by the failure to change her pads.

Wiltshire Council has now launched a safeguarding investigation into her experience at the home.

Miranda House is owned and run by Aria Care Group, which operates more than 60 homes across England, Scotland and Jersey.

Hurst is a former director of the international disability rights network Disability Awareness in Action (DAA) and former vice-chair of Disabled Peoples’ International, and she was heavily involved in lobbying the United Nations (UN) for nearly 20 years to introduce a disability rights convention, receiving letters from disabled people all over the world about her campaign, which she shared with the UN.

The UN Convention on the Rights of Persons with Disabilities was eventually adopted in 2006 and entered into force in 2008.

A former chair of the British Council of Disabled People and Greenwich Association of Disabled People in the 1980s, she has fought for disabled people’s rights throughout her adult life.

She has always been known as a forthright, formidable, and charismatic campaigner – she once heckled prime minister Tony Blair at an event in 10 Downing Street – and says she now wants to use her final years to highlight the appalling state of social care.

She spent 12 days in the care home while her support needs were being assessed.

Hurst, who was awarded a CBE in 2008, said: “I felt impotent and lonely and depressed. It was terrible.”

She said she contacted Disability News Service (DNS) about her “dreadful” and “terrifying” experience because she wanted to publicise the impact of the social care crisis on disabled people who rely on care and support.

Hurst, who nearly died last Christmas from sepsis, pneumonia and flu, told DNS: “I am very angry; the whole of the social care system is engineered to discriminate.

I am hoping you will write a story, but I want to make sure it gets to people who will then do something.

This must get on the radio or television, so people begin to talk about the treatment of disabled people.

I don’t care about me anymore, but I do care about other disabled people.

I don’t want something done about my situation, I want something done about social care, even if it’s the last thing I do.

I want people to understand how terrible things are. The discrimination against us is quite unbelievable.

I travelled the world visiting residential homes, but I am shocked that in Britain today we are treating people in the way we are in these homes and in social care and in our own homes.”

She is now living back at home in Wiltshire, but still relies on 24-hour care, with her health and care needs funded by an NHS Continuing Healthcare package from Bath and North East Somerset, Swindon and Wiltshire Integrated Care Board.

The family’s concerns have been passed on by the care board to Wiltshire Council.

Cllr Gordon King, the council’s cabinet member for adult social care, said: “Everyone has the right to expect the highest standards of care and support when staying in a care home.

When concerns are raised and we are made aware, Wiltshire Council will carry out a safeguarding investigation and support a thorough review of the issues.

We have initiated a safeguarding investigation based on the information that has been shared.

Where care is funded by health services, the integrated care board and Wiltshire Council work closely together to respond to concerns, ensuring they are properly addressed and that the individual raising them is kept informed throughout the process.”

A spokesperson for Miranda House said: “There is nothing more important to us than the health and wellbeing of the people in our home.

While we were sorry to receive this feedback from Ms Hurst, her account differs to our records and is in stark contrast to the typical positive comments we receive from residents and their loved ones.

The home has a 9.5 rating on the independent comparison website carehome.co.uk and is often complimented for our caring and supportive staff team.

Throughout her 12 days in our home, we had been in close communication with NHS Bath and North East Somerset, Swindon and Wiltshire Integrated Care Board, who organised Ms Hurst’s care.

We are confident our team did everything they could to respond to her unique needs with compassionate care.”

Bath and North East Somerset, Swindon and Wiltshire Integrated Care Board refused to comment directly on the complaint made by Rachel Hurst due to patient confidentiality, even though she had made it clear she was happy for DNS to report her case and for the board to discuss it with DNS.

Instead, it released the following statement: “As commissioners of local health and care services, we expect our provider partners – including those outside of the NHS, such as care home residences – to maintain the highest possible standards, and to treat all patients with kindness, dignity and respect.

Where care falls below the expectations of patients and their families, we will investigate and work alongside providers to implement tangible improvements which not only benefit the individual, but also prevent similar situations from occurring.

We strongly encourage any patients who have concerns about their care to reach out to us through our Patient Advice and Liaison Team as early as possible so that we can step in and take action without delay.”

6 November 2025

 

 

Tens of thousands tell government: We reject any plans to cut PIP

Tens of thousands of disabled people and allies have made clear to the government that they reject any plans to cut spending on personal independence payment (PIP) and other disability-related support.

The views came in response to a public consultation on March’s Pathways to Work green paper, with the government publishing its summary of those responses on 30 October.

The consultation, which ran until the end of June, received nearly 48,000 responses, including nearly 900 organisations.

Out of nearly 15,000 direct responses to a consultation question on the government’s original plans to cut PIP entitlement – which were later dropped after a backbench rebellion – more than half (52 per cent) called for the current criteria to be maintained, while 37 per cent highlighted the financial impact of losing PIP, and 18 per cent pointed to the mental health impacts of such a loss.

It is not possible from the document to measure how many respondents in total opposed cuts to PIP because of the way the Department for Work and Pensions (DWP) produced its report.

But in addition to the 15,000 direct responses, DWP also received more than 33,000 other responses – coordinated by three outside organisations – which did not reply directly to the questions posed in the consultation.

Again, DWP did not attempt to calculate how many of these responses opposed cuts to PIP, but it said there was “broad opposition to changes to the value or eligibility of PIP”.

It said these responses also opposed stopping disabled people under 22 from receiving the health element of universal credit, another reform proposed in the Pathways to Work green paper.

Opposition to this change was also overwhelming among those who responded directly to the consultation questions, with more than 42 per cent saying support should be based on need, not age, and more than 12 per cent highlighting that delaying access to the health element would cause financial hardship for young people and increase their risk of poverty.

The document appears to suggest that just four per cent of respondents backed delaying the payments until 22.

Elsewhere in the government’s consultation response, thousands of disabled people and allies made clear to DWP that if it wanted to improve its “current approach to safeguarding people who use our services”, it should abandon any cuts, ensure “financial stability”, and reform the assessment process to ensure “fair, transparent, unintrusive, individualised assessments delivered by trained medical professionals”.

Meanwhile, the government has all but confirmed that it has dropped its plans for a white paper based on many of the Pathways to Work proposals and has decided to proceed instead by announcing future proposals individually.

In response to last week’s Disability News Service (DNS) report that the white paper had been dropped, DWP eventually produced the following statement: “Today, we published the response to the Pathways to Work Green Paper and have already put in place the equivalent of over 1,000 full-time Pathways to Work advisers across Britain to help disabled people into work, as well as investing £1 billion a year for employment support by the end of the decade.

We have also launched the Timms Review to ensure PIP is fair and fit for the future and are increasing the number of health assessments that are being conducted in person.

We will be bringing forward other policy updates in due course.”

Following a DNS briefing last week, the Liberal Democrat work and pensions spokesperson Steve Darling asked Sir Stephen when the white paper would be published.

In his written response on Monday – which mirrored the statement given to DNS – Sir Stephen failed to mention the white paper but instead said DWP had appointed new Pathways to Work advisers and launched his PIP review (see separate story), adding: “We will be bringing forward other policy updates in due course.”

Further evidence that the white paper has been scrapped came in updated terms of reference for the PIP review.

The original terms of reference (PDF) made two mentions of the white paper, but both of these have been removed from the updated terms of reference.

The Benefits and Work website said the backbench rebellion over PIP appeared to have “put ministers off the idea of launching another full scale attack on benefits” and instead seemed to have persuaded them to “switch to guerilla tactics, choosing smaller individual targets which they believe will be easier to achieve”.

6 November 2025

 

 

Other disability-related stories covered by mainstream media this week

Sickness benefits claimants will no longer be able to access subsidised luxury cars under planned changes to the Motability scheme, it has been reported. Rachel Reeves is expected to announce sweeping reforms to the car scheme, which will mean benefits claimants will no longer be able to access high end models, such as BMWs, Mercedes and Audis. The chancellor will also cut back perks offered under the programme, including overseas breakdown cover and insurance that covers up to three different drivers: https://archive.ph/EcI44

Lancashire’s Reform-run council has been accused of “selling off the family silver” through its plans to save £4 million a year by closing five council-run care homes and five day centres and moving residents into the private sector. Questions are also being asked about a potential conflict of interest involving Reform’s cabinet member for social care, who owns a private care company with his wife: https://www.theguardian.com/politics/2025/nov/05/lancashires-reform-run-council-plans-to-close-care-homes-to-save-4m-a-year

6 November 2025

 

News provided by John Pring at www.disabilitynewsservice.com

 

 

Oct 302025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

DWP’s plans ‘in tatters’ as McFadden scraps white paper on further disability cuts 1

Shocking’ figures show parents linked to DWP service face death rates up to three times higher 3

Former detective exposes culture of disability discrimination within ‘institutionally disablist’ Met 6

Committee calls cuts bill ‘discriminatory’, even though all its Labour MPs voted for it 10

Disabled people warn of ‘severe’ consequences if chancellor removes Motability VAT exemption 13

Disabled people face ‘systemic’ barriers in accessing community equipment, parliamentary inquiry finds 16

Regulator’s annual report shows impact of social care crisis on disabled people 18

Other disability-related stories covered by mainstream media this week 19

 

 

DWP’s plans ‘in tatters’ as McFadden scraps white paper on further disability cuts

Ministers have dumped plans for a major white paper containing a swathe of further cuts and reforms to disability benefits, following months of activism by disabled people and allies that forced the government into a major U-turn this summer.

Work and pensions secretary Pat McFadden, who only took on the role last month, confirmed the move in a meeting with representatives of disabled people’s organisations (DPOs) earlier this month.

One DPO said yesterday (Wednesday) that the admission was a “major success” for disabled people who fought the summer cuts bill.

But DPOs also warned that activists would need to keep up the pressure on ministers because McFadden had made it clear that, despite abandoning the white paper – which is likely to have significant political implications for the Labour government – individual measures would be taken forward.

He insisted in the meeting – first revealed this week by Greater Manchester Coalition of Disabled People – that further reforms would go ahead, but they would be introduced individually rather than all together in a white paper.

The white paper was set to be based on many of the measures outlined in the Pathways to Work green paper, and responses to a subsequent public consultation.

The results of that consultation should be published before the end of this year.

The decision to bin the white paper means that many of the reforms suggested in March’s green paper – including removing the health element of universal credit for those under 22; reform, and possibly cuts, to Access to Work; a time-limited replacement for contributory employment and support allowance; scrapping the work capability assessment; and changes to the safeguarding, conditionality and sanctions regimes – are likely to be announced separately over the coming months.

Some – but not all – of the reforms will still require legislation.

McFadden’s admission that he had dumped the white paper was made in a meeting on 14 October with Fazilet Hadi and Svetlana Kotova from umbrella organisation DPO Forum England.

Hadi, head of policy for Disability Rights UK, told Disability News Service (DNS): “I definitely think that the amazing campaigning from disabled people and our allies against the PIP cuts has left the government feeling very bruised.

The change of heart in publishing a DWP white paper, and the delay in launching the SEND white paper, bear this out.

Having said this, Pat McFadden has been moved to DWP to drive through cuts to social security, so the lack of a white paper doesn’t mean that there won’t be further threats to the benefits of disabled people.

It just means that those threats won’t all come at once.”

Kotova, director of campaigns and justice at Inclusion London, agreed.

She said: “There is a pause, but it does not mean reforms won’t be coming.

And we need to keep the pressure and persuade or force the government to switch its focus from cutting benefits or ‘fixing us’ to be more work ready to putting resources and its attention to making workplaces more inclusive.”

Among their arguments in the meeting, she said, was for the government to move money from employment support towards the Access to Work scheme.

Steve Darling, the Liberal Democrat work and pensions spokesperson, has lodged a parliamentary question about the “deeply disturbing” situation after being alerted by DNS.

He said: “At the time of a cost-of-living crisis, it is concerning that the secretary of state could be moving away from a more thoughtful, considered approach, to one more driven by cuts than by strategy.

This will only add to the stress and uncertainty that disabled people are facing with the threat of more cuts to disability benefits next year.

I have therefore asked the secretary of state a named day parliamentary question to find out when (if at all!) the white paper will be published, to try to shed some light on this fraught situation.”

Rick Burgess, from Greater Manchester Coalition of Disabled People, who first revealed publicly that the white paper had been dumped, told DNS: “They are not confident that they will get a big piece of legislation through parliament anymore.

It shows we really scared them. It’s a huge embarrassment for them. All their plans are in tatters, and they are afraid of losing another showdown in parliament.

A Starmer government couldn’t survive another drubbing.”

But he said he did not think ministers had changed their attitudes towards welfare reform, only that they were not confident they could push a large bill through parliament.

And he said it would be much harder for disabled people to stop a stream of smaller reforms, and that “keeping track of them is going to be really tricky”.

Linda Burnip, co-founder of Disabled People Against Cuts, said the government’s move to drop the white paper was “obviously a major success for disability rights activists and the many months of campaigning”.

But she said it appeared likely that ministers would use secondary legislation to “sneak things through in dribs and drabs and hope changes won’t be noticed”.

McFadden told Fazilet Hadi and Svetlana Kotova at the meeting that no decisions had yet been taken on barring under-22s from the health component of universal credit, and that it was a priority of his to get more young people into work.

They said he seemed to indicate that time-limiting contributory benefits would be taken forward relatively soon.

Hadi said: “We emphasised the need for government to join up its policies on disabled people and to coproduce solutions with us.

We urged him to move funding to the Access to Work scheme from the additional money being spent on employment support.”

Reforms – and almost certainly cuts – to personal independence payment are expected to follow next autumn, following a review being headed by Sir Stephen Timms, the minister for social security and disability.

Sir Stephen today (Thursday) launched the review, and announced his disabled co-chairs – Dr Clenton Farquharson and Sharon Brennan – as well as a recruitment process for the 12 members of a steering group that will jointly lead the review.

He said the majority of this steering group would be disabled people or representatives of DPOs.

DWP had not commented on McFadden’s admission by noon today (Thursday).

30 October 2025

 

 

Shocking’ figures show parents linked to DWP service face death rates up to three times higher

Parents who pay to support a child through the Department for Work and Pensions (DWP) and its Child Maintenance Service (CMS) face death rates up to three times higher than others the same age, according to “shocking” and “deeply troubling” new figures.

Analysis by Disability News Service (DNS) has shown that, for every age group between 20 and 54, those who use the service – known as “paying parents”* – face a much higher rate of death than those of the same age who do not have to deal with the CMS.

DNS carried out the analysis using figures obtained from DWP through a freedom of information request.

The request followed concerns raised by campaigners who have called for an inquiry into the deaths of parents driven to take their own lives by DWP’s refusal to correct errors in child support demands.

The figures, which are particularly exaggerated for younger age groups, have been passed to the Commons work and pensions committee, which is at the early stages of an inquiry into concerns about CMS.

Among the inquiry’s aims will be how to “improve the way it deals with families”, and concerns over how CMS calculates payments, and enforcement of its decisions.

The DNS analysis shows that, for all those aged 20 to 24 in England and Wales, the rate of deaths in 2024 was 0.04 per cent, compared with 0.13 per cent for CMS paying parents (more than three times higher).

For those aged 25 to 29, the rate of death was more than twice as high for paying parents, and for those 30 to 34 it was twice as high (0.12 per cent versus 0.06 per cent).

The difference in death rates narrows for older age groups, but there is still a substantial difference for every group analysed by DNS, with CMS paying parents aged 50 to 54 facing a death rate of 0.46 per cent in 2024, compared with 0.34 per cent for all adults in that age group.

Results for 2022 and 2023 show similar, striking differences.

Over those three years, there is not a single age group between 20 and 54 – the only groups examined in the analysis – where the death rates are not higher for paying parents than for all adults in England and Wales.

Although the figures do not show how many of these deaths were suicides, they do add strong evidence to the claims of campaigners who believe the higher rates of death for paying parents are at least partly caused by errors by CMS and its toxic culture, including its refusal to correct its mistakes. 

DWP said this week that it was carrying out reforms aimed at streamlining CMS but that it did not “recognise” the DNS figures or any suggestion of a causal link between the actions and culture of CMS and the deaths of paying parents, although it did not point out any errors in the DNS calculations.

Ian Briggs, from research and campaign group STOPS (StopSuicides UK), which focuses on the harm caused by CMS, said: “I, and many others, have long known that the CMS and the DWP have been responsible for driving many parents to suicide.

For years we have tried to highlight this to the DWP, yet every attempt is met with the same denial – that there is no link between the CMS and suicides.

Even when presented with clear and credible evidence gathered by the STOPS group, the official response from ministers has remained one of outright dismissal.”

His son Gavin took his own life five years ago.

The coroner at Gavin’s inquest refused to investigate his father’s claims that the actions of the CMS had contributed to his decision to take his own life, even though the agency had wrongly claimed he owed £16,000 in support payments, after claiming his income was £76,000 rather than the £26,000 it was in reality.

Ian Briggs said this week: “The mortality rates recently revealed through John’s** research and exposed by Disability News Service cannot all be explained away as coincidence.

While not every death may be due to suicide, these figures reveal a deeply troubling pattern that demands urgent scrutiny.

At some point, there must be a full and independent public inquiry into these disturbing facts and the systemic failures within the CMS and DWP that continue to destroy lives and families.

I would like to personally thank John and Disability News Service for… exposing these shocking mortality rates, and for giving a voice to the countless families – like mine – who have suffered unimaginable loss.”

Craig Bulman, who was left with PTSD after the Child Support Agency mishandled his case – the agency, the predecessor of CMS, eventually paid him a £5,000 consolatory payment – said the figures uncovered by DNS were “shocking”.

He told DNS: “Even allowing for statistical margins, the death rates you’ve calculated are deeply disturbing and point to something seriously wrong within the Child Maintenance Service.”

The Child Support Agency’s failings left Bulman homeless, triggered a mental breakdown, and caused the loss of his job.

He said this week: “These figures confirm what families have been warning for years – that the Child Maintenance Service is operating without proper oversight or duty of care.

Death rates among paying parents are up to three times higher than the national average, and yet the DWP has failed to investigate or publish these findings. 

This now warrants an independent inquiry under the Inquiries Act 2005.”

In January 2023, during the final session of a previous inquiry into CMS by the Commons work and pensions committee, Labour MP Debbie Abrahams told of a paying parent whose arrears had been inaccurately assessed “and the frustration that he found ultimately led to him taking his life”.

She said his mother had previously written to DWP “expressing real concerns about mental health” but there had been no reply.

She added: “This is not the first time. We had a panel before Christmas that also provided data about the suicides of paying parents who were inaccurately assessed in terms of the arrears that they owed.

This is tens of thousands of pounds that they said that they owe, leaving literally pounds for them to exist on.”

She asked Tory work and pensions minister Viscount Younger at the time if DWP collected data on suicides of paying parents.

He told her: “Could I just say that, being new into the department, I am already aware, having seen some of the correspondence that I have had to look at and sign off on, of some absolutely tragic cases?

It is absolutely appalling that cases can lead to people taking their own lives.

That is dreadful and we must look at all ways in which we can avoid that or have systems and processes that do not lead to that.”

Despite those comments, a DWP spokesperson said this week: “Over 780,000 people engage with the Child Maintenance Service, many of whom are experiencing a difficult time in their lives, and all staff are trained to support vulnerable customers.

We do not recognise this data or suggestions of a causal link between the CMS and deaths among parents.”

*Child maintenance covers how a child’s living costs are paid when one of the parents does not live with the child

**DNS editor John Pring

***The following organisations are among those that might be able to offer support if you have been affected by the issues raised in this article:  MindPapyrusRethinkSamaritans, and SOS Silence of Suicide

30 October 2025

 

 

Former detective exposes culture of disability discrimination within ‘institutionally disablist’ Met

A culture of institutional disability discrimination within the Metropolitan police is exposed today by the former head of its disabled staff association.

Dave Campbell, who retired this year after serving 32 years as a police officer, has told Disability News Service (DNS) that he believes disability discrimination within the force is rampant and that the Met is institutionally disablist.

He believes this “corporate culture” impacts how the force engages with disabled members of the public.

Campbell was chair of the Met’s Disabled Staff Association (DSA) for six years, and he was also vice-president of the Disabled Police Association of England and Wales.

His disclosures come only days after DNS revealed that prosecutions of disability hate crime across the country were continuing to plummet, with police forces in England and Wales passing on just a tiny proportion of recorded cases to prosecutors.

For six years, Campbell repeatedly tried to persuade the Metropolitan Police Service (MPS) to act on his concerns, before his retirement earlier this year.

It was his intervention that ensured the recent Casey review of the force’s internal culture and standards of behaviour examined the treatment of disabled people, when its initial focus was on racism, sexism and homophobia.

He believes the review provided an “alarming insight into how disabled people feel about their place in the organisation”, as he told Met commissioner Sir Mark Rowley in a letter last year.

He has told DNS that the upper levels of the Met have made it clear through their actions and inflexible policies – which he says marginalise disabled staff, and stem from outdated attitudes – that they do not want people who become disabled to continue serving as police officers in the force.

He says several disabled officers and staff have left the force because of their disability-related treatment and have written directly to the commissioner expressing their “despair and concerns”, without receiving any acknowledgement.

Over the four years between 2019 and 2023, he says, more than 200 disability discrimination employment tribunal claims were taken against the Met, including a significant number which included claims of race or gender discrimination.

The Casey review found an even higher number – 358 – in the five years between 2017-18 and 2021-22, but it was criticised by disabled campaigners for concluding that MPS was institutionally racist, sexist and homophobic, but not that it was institutionally disablist.

Campbell believes the number of disability discrimination tribunal cases increased after the Casey review by up to 60 per cent in 2023-24 compared to the previous year, while the DSA received hundreds of emails from distressed colleagues about the way they were being treated by their managers.

He has told Sir Mark that disability-led internal grievances are also at a high level, while many of his members had “no confidence or trust in the grievance management process” or in the ability of the Culture, Diversity and Inclusion directorate – set up after the Casey review – to produce change.

In the wake of Casey’s report, Campbell – as DSA chair – commissioned an independent review of disability inclusion and workplace adjustments in the force, by the Business Disability Forum (BDF), which reported its findings in September 2024.

Disabled colleagues in the DSA were asked if they had witnessed or personally experienced unfair treatment at work through disability-related harassment, bullying or discrimination, and 358 of the 775 who responded to the survey said yes (46 per cent), and another 123 (16 per cent) said maybe, a total of 62 per cent.

Of 504 police officers, 49 per cent said yes, and 15 per cent said maybe, a total of 64 per cent.

Of the 775 responses from disabled officers and civilian staff, less than 20 per cent (160) agreed with the statement: “MPS is an organisation that recognises and values disabled people.”

And just 65 (eight per cent) agreed that “feedback and complaints are listened to”.

One respondent said: “If you treated any of the other protected characteristics as you did disability then there would be uproar and heads would roll.”

Campbell believes the BDF report supports the view that MPS is institutionally disablist.

He told Sir Mark in last year’s letter: “In my experience Disability discrimination in the MPS is viewed less significantly and addressed differently in comparison to Race, Homophobia, Gender or any other type of Discrimination…”

In an earlier letter to Sir Mark, in 2022, Campbell told him: “There needs to be a change in attitudes [towards disabled officers] and an end to conscious labelling, as sick, lame, lazy, shirker, which are all derogatory terms yet seemingly acceptable…”

He has yet to receive any “tangible” response to the concerns he raised in last year’s letter and the survey report.

Campbell, a detective sergeant before his retirement, has himself twice taken successful action against the Met for disability discrimination, winning the first case at tribunal and then securing an MPS settlement before the start of a tribunal for the second case.

He describes himself as a person of ethnic origin, and has experienced intersectional discrimination, which he says is widespread in the Met.

He said the same complaints are being made “time and time again” at tribunal and through the force’s internal grievance process, which shows there is a “systemic” problem and failure to address these issues through an absence of “corporate memory” and a lack of “morality”.

Currently, about 3,500 police officers have adjustments made for them to allow them to continue in their roles, he said, out of about 36,000 officers in total across the force.

Campbell believes the number of MPS disabled officers and civilian staff may be as high as 10,000 – almost a quarter of the workforce – because many staff do not share their impairment with the force “due to concerns of how they will be treated”.

The Met’s DSA has more than 6,500 members and has 37 peer-to-peer support networks for disabled staff.

Campbell says he has increasingly been coming across incidents where the force’s occupational health department is making recommendations for adjustments to be made for officers who become disabled – often caused by their duties – but managers are refusing to agree to these adjustments.

Instead, officers are often told: “If you cannot do the job then you should just leave,” or: “This isn’t the right job for you.”

He told DNS: “We are just hitting a brick wall. This is about holding the police to account for systemic behaviour both internally and externally.

If these attitudes exist towards disabled people in the workforce, what hopes do disabled people have when they become victims of crime?”

Louise Holden, Inclusion London’s senior policy officer for disabled people and crime, said: “I admire Dave Campbell and his tireless work within a disablist organisation.

I share Mr Campbell’s concerns about how the Met treat disabled victims when their attitude to their own disabled staff is so appalling.

Things have gotten worse since the A New Met for London plan following the Casey review.

The work Inclusion London was involved in stopped and the new structure is a closed shop.

Community confidence is at an all-time low.

There has been no follow-up to the Casey review and with the Met decision to stop investigating non-hate crime incidents, without any consultation, it’s clear the Met is just not interested in disability issues.

There has been no radical reform, only half-baked gestures and platitudes that amount to nothing.

We are calling for renewed engagement with us, so we can support the Met with our expert knowledge on these issues.

I hope the Met is ashamed of how they have behaved since the Casey review and want to work with us again.”

Commander Simon Messinger, the Met’s professionalism and senior lead for disability, said: “We are fully committed to driving positive change across the Met and fostering a culture of inclusion, and have taken significant steps to improve how we support disabled colleagues.

This progress has helped us to achieve Disability Confident level three status, the highest level of recognition within that scheme, which reflects our determination to improve how we recruit, retain, and support our staff.

We know there is much more to be done and will continue to work with the Met police Disabled Staff Association, and partners such as the Business Disability Forum, to drive further progress.”

A spokesperson for the mayor of London said: “The mayor is clear there is no place for harassment or discrimination in the workplace and is committed to working with the Met police to deliver a New Met for London where everyone can thrive.

Since the Baroness Casey review in 2023 the Met has implemented a number of improvements for disabled employees, including the introduction of disability passports, Disability Smart assessments and the force is now a Disability Confident employer, improving how they recruit, retain and develop disabled staff.

But there is more to do and the Met is working closely with the Disability Independent Advisory Group and the new chair of its Disabled Staff Association to listen and act on concerns to deliver a fairer and more inclusive Met.”

*If you have information about a police officer or member of staff who works for the Met and is corrupt or abusing their position and power, you can call the force’s anti-corruption and abuse hotline anonymously on 0800 085 0000

30 October 2025

 

 

Committee calls cuts bill ‘discriminatory’, even though all its Labour MPs voted for it

A Labour-led committee of MPs has called the government’s universal credit cuts act “discriminatory” and warned that it will push disabled people into poverty, despite every one of its Labour members voting for the legislation in July.

The Universal Credit Act will see the health element of universal credit halved for most new claimants from 6 April next year, from £105 to £54 a week.

All seven Labour MPs on the committee* voted for this cut in July.

But Labour’s Debbie Abrahams, who chairs the committee, said this week: “This is not only discriminatory, but without mitigations, will potentially push more people with disabilities and health conditions into poverty, exacerbating their condition and pushing them further away from the labour market.”

She was commenting on the publication of the government’s response to the committee’s report on the Pathways to Work green paper.

Her committee’s report had called on the government to delay the cut to the health element until it had carried out an “independent and comprehensive assessment of the impact the change could have on disabled people”.

But in this week’s response, the Department for Work and Pensions (DWP) dismissed those concerns.

Instead, it pointed to the “sustained, above inflation increase” to the standard allowance of universal credit (UC), which will also be introduced through the bill.

It said that this, together with the cut to the health element, would address “perverse incentives in the UC system and better encourages those who can work to enter or return to employment”.

Asked why she had voted for the cut to the health element when she thought it was discriminatory and would push more disabled people into poverty, Abrahams told Disability News Service (DNS) in a statement: “I worked very hard to secure major concessions on removing the cuts to PIP and people currently on UC health in the welfare bill.

The bill isn’t perfect, and that was reflected in the work and pensions Pathways to Work report and its recommendations.

However, voting against the bill would have meant that the increase in the standard allowance wouldn’t have gone ahead, and that was seen as a major positive aspect of the bill.

This increase is not just for this year, but for each year until the end of this parliament.

I am still continuing to work hard on securing mitigations around the reduction in support for newly disabled people from April next year and I remain committed to ensuring disabled people across the country have access to the support they need.”

Meanwhile, DWP has refused to explain to the committee what assessment it made of the bill’s impact on safeguarding, before the legislation was introduced to parliament earlier this year.

The bill had originally included steep cuts to personal independence payment (PIP), before a backbench Labour rebellion – following three months of activism from disabled people and allies – led to those measures being removed.

But there has been almost no discussion in parliament – and little or no information from ministers – on the bill’s potential impact on safeguarding claimants.

In its response to the committee’s report, DWP has made no mention of safeguarding, although it said that it had carried out an equality impact assessment for the bill.

But the impact assessments published on parliament’s website make no reference to safeguarding.

Asked by DNS why it failed to respond properly to the committee’s recommendation to release its assessment of the bill’s impact on safeguarding, and whether it did assess the safeguarding implications of the original bill, DWP said it was looking to improve its safeguarding approach, which included a review of the green paper consultation responses.

A DWP spokesperson said: “Our welfare reforms package was appropriately advised and numerous protections were baked into our plans.

We are shifting our focus from welfare to work, skills, and opportunities, so more people can move out of poverty and into good, secure jobs as part of our Plan for Change – backed by £1 billion a year for employment support by the end of the decade.”

Grassroots groups of disabled people, such as Black TriangleDisabled People Against Cutsthe Mental Health Resistance Network, and the Spartacus network, spent years highlighting deaths linked to DWP’s actions.

Concerns have also been raised by relatives who have called for action after the deaths of their family members.

Some of the evidence linking DWP with the deaths of benefit claimants has come through prevention of future deaths reports written by coroners, several of which only emerged years after they were written.

Other evidence of persistent DWP safeguarding flaws has emerged through freedom of information requests to the department, which have revealed how hundreds of recommendations for improvements have been made by DWP’s own secret reviews into the deaths of claimants.

Some of these reviews showed DWP staff continuing to make the same fatal errors, year after year.

The evidence collected by DNS and others, stretching back more than a decade, has shown how DWP repeatedly ignored recommendations to improve the safety of its disability benefits assessment system, leading to countless avoidable deaths.

It also shows how DWP hid evidence from independent reviews, and how the department failed to keep track of the actions taken in response to recommendations made by its own secret reviews.

Evidence also demonstrates that the cultural problems within DWP extend far beyond the assessment system, touching all aspects of its dealings with disabled people in the social security system.

The evidence, compiled over the last decade by DNS and other journalists, academics and activists, shows systemic negligence by DWP, a culture of cover-up and denial, and a refusal to accept that the department has a duty of care to those disabled people claiming support through the social security system.

Much of that evidence has been brought together in a detailed timeline, as part of the Deaths by Welfare project headed by Dr China Mills and supported by Healing Justice Ldn, which works with marginalised and oppressed communities.

*Debbie Abrahams; Johanna Baxter; Damien Egan; Gill German; Amanda Hack; Frank McNally; and David Pinto-Duschinsky

**The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP’s actions and failings, is published by Pluto Press

30 October 2025

 

 

Disabled people warn of ‘severe’ consequences if chancellor removes Motability VAT exemption

Disabled people have warned of “severe” consequences if the chancellor goes ahead with reported plans to remove the Motability car scheme’s VAT exemption in next month’s budget.

Disability News Service (DNS) reported last week how the company that runs the scheme, Motability Operations, had warned that removing the VAT tax break entirely could impose an upfront cost of at least £3,000 on even the cheapest cars it offers.

There is no certainty that the chancellor will go ahead with removing the tax exemption entirely – which was revealed by the Times – and she may abandon the plans completely.

But the minister for social security and disability, Sir Stephen Timms, failed to deny plans to target the VAT exemption when asked by disabled Labour MP Emma Lewell on Monday about potential cuts to the scheme.

Instead, Sir Stephen said again that there would be no changes to personal independence payment until next autumn.

Yesterday, a Reform UK press conference on the party’s plans to slash disability benefits – particularly personal independence payment (PIP) – saw the party target the Motability scheme.

The party’s work and pensions spokesperson in the Commons, Lee Anderson, said the scheme had “got completely out of hand” and was “an absolute scandal”, and he suggested that all those receiving Motability cars should only be able to secure a “blue three-wheeler”*.

He said: “What’s wrong with that? Let’s go back to that.”

Meanwhile, disabled people who rely on Motability to maintain their independence have told DNS this week of the drastic impact that increased costs could have on their ability to afford a car through the scheme, and how this would affect their ability to work, enjoy leisure opportunities, and attend medical appointments.

Julia Dalton, a Motability customer for more than 40 years, relies on an adapted vehicle, which she says has allowed her “to work for over four decades, contribute taxes, and live independently” in east Yorkshire.

As an electric wheelchair-user, she needs a large vehicle with a hoist to lift her wheelchair into the car.

She said: “Without Motability, I could never have afforded a suitable vehicle.

It is not possible for me to use a cheap second-hand car because if it breaks down, I cannot simply use a hire car that is not adapted for my needs.

Without a reliable vehicle I would not have been able to get to work and would likely have lost my job.

This scheme has protected my independence, wellbeing, and ability to contribute”.

She says that advance payments – on top of contributing the enhanced rate mobility component of PIP every month – have risen significantly in recent years.

Her latest vehicle in March cost her £4,000 in an advanced payment as well as £1,500 for essential adaptations.

She said: “I am managing financially, but even I would struggle to pay thousands more on top.

If someone like me is at risk of coming off the scheme, what happens to those with less support?

The consequences are severe: disabled people stuck at home; people losing work because they cannot travel; missed medical appointments; isolation.

Motability is not a luxury. It is a lifeline.”

She added: “If exemptions are removed or costs continue to rise, we risk destroying a system that enables disabled people to live, work, and participate fully in society.

I am deeply grateful for Motability. I want to see it protected for the future, so others can have the same opportunities that I had.”

Emma, from Leicester, told DNS that her Motability wheelchair-accessible vehicle (WAV) – which needed an advance payment of £4,500 – had made “a huge positive difference” to her life, and allowed her to continue to visit her dad after he had a stroke, firstly while he was in hospital, and then at home.

She said: “WAV taxis are expensive and difficult to arrange, and using public transport would have been impossible for me health-wise.

Without that access, he might have declined further or needed residential care.

The scheme has literally kept our family connected and independent.”

She said the knock-on effects of removing the VAT exemption – and the insurance premium tax, which is reportedly also being considered – would “make it even harder for disabled people to stay mobile”.

She said: “The knock-on effects would be huge — more reliance on carers, increased pressure on health and social care services, and greater difficulty getting to appointments or even maintaining social contact and contributions to society.

If the tax relief were removed, I simply wouldn’t be able to afford a vehicle and would be stuck in my house even more.”

Richard, a Motability-user for 30 years, from the West Midlands, told DNS that the scheme was vital as a wheelchair-user living in inaccessible housing, and that he and many others would be forced to leave the scheme because it would become unaffordable if its VAT exemption was removed.

He has a progressive, neurological muscle-wasting condition and uses his Motability car to drive to a pool to swim, which allows him to keep the strength in his shoulders that he needs to pull himself up and down the stairs of his home.

Without the car, he would not be able to use the stairs and would end up in expensive extra care housing or a nursing home.

He said: “Being stuck at home would be very detrimental to my mental health.

It will have similar effects on many, especially those who would have to give up work due to unaffordable initial payments.”

April, who has been a Motability customer for 15 years and lives in Lancashire, said the scheme has allowed her to maintain her independence and job and “gets me to and from my workplace safely and stress free”.

She has a small automatic hatchback which now requires a £1,000 advanced payment, when previously there was no advance payment required.

She said: “I fear these government proposals will make Motability pass these costs on to the scheme users – to the detriment of those struggling on low incomes and those needing larger adapted vehicles.

The scheme must be preserved for those of us that need it to maintain our independence, to work, attend appointments, and to live decently, with dignity and safety.”

Michael Newbold, from Staffordshire, a Motability customer for more than 20 years, said the scheme was “essential” for him and his disabled wife.

He said: “I need a car for appointments and shopping, also for leisure.”

They have already had to cope with the council stopping paying for a personal alarm, and for the insurance on his stairlift.

He said: “It’s like little by little they are taking all the things that make life easier.

Most people, in my opinion, will not be able to afford the VAT rise if they are in a similar position as me.”

Another customer, Phil, told DNS that he and his wife Kath would be “totally screwed” without their Motability vehicle.

They are both disabled, but it is Kath who is the Motability customer as she uses a powerchair following a spinal stroke, so she needs a WAV.

Phil said: “We had to find a £4,000 down payment for our WAV and when it has to go back [at the end of the lease] we’ll have to find the same if not more for the next vehicle.

Adding VAT on top would make it unaffordable for us.”

Without the car, he said, they would be “totally isolated”, and they already both struggle with their mental health.

He said: “I can only believe others in the disabled community will be affected in the same way.

My wife and I are from Bristol and it’s a city with an awful bus service so another reason the Motability scheme is so vital for us.”

*A reference to the Invacar that was provided by the government to disabled people up until the late 1970s, when it was replaced by the Motability scheme

**Motability Foundation, the charity that oversees the car scheme, is a DNS subscriber

30 October 2025

 

 

Disabled people face ‘systemic’ barriers in accessing community equipment, parliamentary inquiry finds

A cross-party group of MPs and peers has called on the government to draw up a national strategy to address the “deeply troubling” and “systemic” barriers that prevent disabled people accessing the equipment they need to live independently.

Hundreds of disabled people and professionals across the UK fed into the inquiry by the all-party parliamentary group for access to disability equipment, which found an “inconsistent” community equipment system that was in crisis due to fragmentation, underinvestment, and a lack of leadership.

The inquiry heard of disabled children missing school because the correct hoists had not arrived; disabled adults unable to live independently and forced out of their jobs because repairs to equipment were taking months; and carers driven to “physical and emotional exhaustion”.

It found too many disabled people faced long delays, unsuitable equipment and “a lack of joined up support” within the system, which provides equipment such as grab rails, hoists, wheelchairs, ramps, specialist mattresses, and assistive technology.

The group’s report includes findings of a survey from more than 600 users of equipment, carers, professionals and equipment-providers.

More than half of equipment-users who took part (55 per cent) said they believed services were worsening.

The same proportion said they did not have access to the equipment they needed.

One equipment-user told the inquiry that the support offered “barely scrapes the barrel of what people actually need to live their everyday lives.”

More than a fifth of those surveyed (22 per cent) said they had waited more than two months to receive their equipment once it had been approved.

The report heard of the experience of Rhys Porter, who has cerebral palsy, and went without essential equipment, including a hoist and home adaptations, for two years.

His parents had to help him use a commode seat in his bedroom and drag him into the family bathroom on a towel once a week.

He was only able to go ahead with vital surgery because the charity Newlife provided him with a portable hoist.

The report calls for a “cohesive” national strategy; funding reform of the current “fragmented” model; action to address lengthy waiting-times for assessments and equipment; improved communication with equipment-users and between local authorities, health bodies, and government departments; a national advisory board with service-user representation; and action to improve reuse and recycling of equipment.

Labour MP Daniel Francis, chair of the all-party group, said: “Across hundreds of testimonies, one message came through loud and clear: the system designed to support disabled children and adults is failing them.

It is failing to deliver equipment on time, failing to provide the right support, and failing to listen to the very people it exists to serve.

Under the current system we’re seeing children missing school, adults being forced out of work and carers injuring themselves.

It’s failing patients, carers, and the sector alike, and it’s high time for the government to get a grip.

Access to community equipment is not privilege, it’s a daily necessity.

We need a national strategy for community equipment and clear leadership and accountability in its delivery.

Ensuring everyone is given the right support at the right time is simply a matter of political will and commitment.”

The Department of Health and Social Care was unable to comment on the report by noon today (Thursday).

30 October 2025

 

 

Regulator’s annual report shows impact of social care crisis on disabled people

An annual report by the care regulator has highlighted how the continuing social care crisis is impacting disabled and older people who need support in their own homes.

The Care Quality Commission said in its annual State of Care report that the health and social care system remained “fragmented and under severe strain”.

It said that demand for local authority-funded support had continued to rise, while the job vacancy rate in adult social care was still three times higher than in the wider employment market.

And it said that more community services were “urgently needed” to support people to stay in their own homes for longer.

The report includes evidence from members of CQC’s Experts by Experience group, which has come from their own experiences of care and support and from talking to other service-users during CQC inspections.

Living in a rural area can particularly affect alternative options if a homecare agency is providing poor care, the report says.

One of the Experts by Experience told CQC: “The only other agency down the road hasn’t got any space for me. Where do you expect me to go?

I’m telling you what’s wrong and the things I’m not happy with, but I don’t feel like I’ve necessarily got a choice to change that.”

CQC’s Experts by Experience said disabled people had told them how they had been “left to sit or lie in soiled or wet clothing for hours while waiting for their care worker to arrive”.

The report says: “As local authorities around the country increasingly look to make savings, it seems likely more will signpost people to support in the community, ration the care they do provide, and reduce the provision of other statutory and non-statutory services.

As well as negatively affecting the health and wellbeing of those in need of social care support, this could increase the pressure on the health and care system and the voluntary, community and social enterprise sector, and further increase the burden on unpaid carers.”

As CQC only began implementing its new single assessment framework in January 2024, it is not possible to directly compare the latest ratings from its inspections with previous years.

Inspections have been focused on services where CQC information suggested people might be at risk.

The ratings produced through the framework for about 3,000 adult social care services (out of a total of about 20,000 services across England) show four per cent were rated inadequate, another 26 per cent were seen as requiring improvement, 67 per cent were rated good, and two per cent were seen as outstanding.

Professor Sir Mike Richards, CQC’s chair, said: “The Casey Commission will be an important step in reforming social care – but it won’t solve the core funding problem.

We continue to call for long-term, sustainable funding for adult social care.”

30 October 2025

 

 

Other disability-related stories covered by mainstream media this week

Reform UK’s draconian plans to scrap the personal independence payment (PIP) for people with anxiety were last night labelled “cruel, heartless and reprehensible”. At a press conference in London, the party vowed to end PIP for claimants with “non-serious anxiety disorders” and introduce more regular reassessments for those who qualify: https://www.mirror.co.uk/news/politics/reform-uks-plans-rip-up-36150700

Journalist and former BBC presenter Mark Mardell was left feeling “humiliated” after he was told he could not board a Turkish Airlines flight due to having Parkinson’s disease and no doctor’s report. The broadcaster was unaware of this requirement and was shocked when he could not board his flight home from Istanbul to Gatwick: https://www.bbc.co.uk/news/articles/ce9dx4zgzjzo

30 October 2025

News provided by John Pring at www.disabilitynewsservice.com

 

Oct 232025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Chancellor’s reported plans to impose VAT on Motability could add £3,000 to even the cheapest cars 1

Psychologists’ charity fails to raise concerns over job coaches in surgeries, weeks after £640K DWP contract 3

Peers derail government plans to hand some DWP staff powers to use force against benefit claimants 5

Reeves refuses to apologise for repeating false claim that social security spending is spiralling 7

Timms goes back on his word by refusing to provide crucial evidence of Access to Work cuts 8

Disabled people describe impact of ‘very unfair’ extra costs caused by DWP’s universal credit migration 9

Ministers’ refusal to raise limit on accessible housing grants is discriminatory, secret reports admits 11

Ministers finally announce progress on ‘liberty safeguards’, but also challenge vital definition 14

Other disability-related stories covered by mainstream media this week 16

 

 

Chancellor’s reported plans to impose VAT on Motability could add £3,000 to even the cheapest cars

The chancellor’s reported plans to target the Motability car scheme for new taxes in next month’s budget by removing its VAT exemption could impose an upfront cost of at least £3,000 on even the cheapest cars it offers, the company has calculated.

Motability Operations spoke out after an article in the Times – which has strong contacts within Whitehall – suggested that Rachel Reeves would be “dramatically reducing an exemption by which cars leased under the scheme do not have to pay VAT or insurance premium tax”.

The Times said that VAT tax breaks “worth about £1 billion a year are set to be scrapped in the budget”.

But targeting the Motability car scheme in next month’s budget by completely removing its VAT exemption would add thousands of pounds every three years to the bills of some of the poorest disabled people in the country.

The potential tax-raising measure – which would be aimed squarely at disabled people – follows months of mounting hostility aimed at disabled people and the Motability scheme in the right-wing media and on social media.

But Motability Operations, the company that runs the scheme, said this week that removing VAT relief “would make cars unaffordable for most disabled people, leaving only the wealthiest able to access the scheme – a result that would fundamentally undermine its purpose”.

It confirmed to Disability News Service (DNS) that, if Reeves placed VAT at 20 per cent on all Motability cars – and assuming no changes elsewhere in the scheme – it would increase the overall cost of a lease over three years by £3,000 for the cheapest cars it offers.

This would mean disabled people would have to find an advance payment of £3,000 for even the cheapest models, on top of having to contribute all their enhanced mobility component of personal independence payment (PIP) to fund their monthly lease payments.

It would mean the scheme would instantly become unaffordable to tens of thousands of disabled people seeking independent mobility.

Motability Operations said the median household income of a disabled person using the scheme is just £18,500, half the UK average.

Graham Footer, chief executive of Disabled Motoring UK (DMUK), told DNS: “DMUK is concerned by the recent reports in the national media that the chancellor is considering making changes to the Motability scheme, including removing the tax breaks.

The fact this is even on the table for consideration is a worry.

If the chancellor goes ahead with the changes, it will have a significant detrimental impact on Motability customers and for many it will put the scheme financially out of reach.”

A Motability Operations spokesperson said: “The scheme operates at scale, allowing bulk purchasing and strong manufacturer discounts.

Removing the zero-rating would erode this efficiency and undermine the social purpose of enabling independence and affordable mobility.

There would also be a knock-on impact to jobs in the automotive sector.”

Motability Foundation*, the charity that oversees the car scheme, has described some of the “recent, misinformed commentary” about the scheme as “profoundly disheartening” and said that it “unfairly stigmatises disabled people”.

It said the scheme “provides a vital service to disabled people, helping them to overcome significant mobility barriers” and “a foundation of independence which also helps to address the transport equity gap”.

Earlier this year, Motability Foundation’s disabled boss hit back at months of “hostile”, “harmful” and inaccurate media reports and online comments about how the scheme is run and its disabled customers.

Chief executive Nigel Fletcher said then that he believed the “climate of stigmatisation” of disabled people “risks rolling back decades of progress in promoting disability inclusion and understanding”.

He told DNS: “It creates an environment where disabled people are scrutinised and made to feel they must justify their right to mobility and participation. This is unacceptable.”

Coverage has included reports of comments made by Conservative leader Kemi Badenoch, who claimed that new Motability vehicles were being leased by people with food intolerances.

Other reports have suggested that Motability vehicles are handed out “free” – rather than in exchange for most or all of the higher rate mobility element of PIP, and sometimes an additional advance payment – and with few if any checks on eligibility, misleading statements that were repeated today (Thursday) by Conservative shadow work and pensions secretary Helen Whately.

There have also been widespread reports in the media and on social media attacking Motability customers and accusing them of abusing the scheme.

*Motability Foundation is a DNS subscriber

23 October 2025

 

 

Psychologists’ charity fails to raise concerns over job coaches in surgeries, weeks after £640K DWP contract

The national charity representing psychologists failed to speak out about the serious risks caused by placing work coaches in GP surgeries, just weeks after it was awarded a £640,000 contract by the Department for Work and Pensions (DWP).

There was alarm among many disabled people when DWP announced earlier this month that it was expanding a programme to “embed” job advisers in GP surgeries, mental health services and other healthcare settings.

They believe that for many disabled claimants of out-of-work benefits, particularly those with mental distress, ill-health and trauma, the idea of facing a DWP officer in a healthcare setting, at a time when they need support rather than pressure to discuss work, would be “horrifying”.

Among those speaking out was Dr Jay Watts, a disabled activist and herself a consultant clinical psychologist, who said: “It’s really dangerous for the government to put work coaches in GP surgeries.”

She said many mental health claimants already find it “scary” to visit their GPs because they “tend not to be believed”, while surveys show a substantial proportion of them are “absolutely terrified of the DWP”.

She said she feared the DWP scheme would prevent many claimants accessing healthcare.

Despite these concerns, the British Psychological Society (BPS) – which represents psychologists – appeared to be broadly supportive of the DWP scheme, in a statement it issued last Thursday (16 October).

It appeared to suggest that the scheme could be useful, given the right training for the job advisers, saying: “While a job adviser could act as an incentive and offer support to those with mental health problems to return to work, it is vital this isn’t to the detriment of a person’s recovery by adding further stress and anxiety.

Ideally, all job advisers should be psychologically informed and work to identify a person’s strengths and support them in managing change.”

But it has now emerged that this statement was published just four weeks after DWP awarded BPS a £641,000 four-year contract to carry out accreditation of the department’s in-house work psychologists.

BPS yesterday (Wednesday) denied any connection between the award of the contract and its statement on the DWP scheme.

But one campaigner, who first spotted the contract award, told Disability News Service this week: “The BPS’s views on employment advisers are totally compromised by this and should not be regarded as objective.”

The grassroots, user-led mental health group Recovery in the Bin (RiTB) added: “The BPS have betrayed every person in need of mental healthcare and social security.

We are being treated like livestock who either produce or are sent to the abattoir.

The NHS will be polluted with work fetishism and people will not trust anything medical professionals do, as everything will be corrupted to a work outcome, instead of what is best for the person.”

Another disabled activist said the BPS response was “appalling” and “completely unethical”.

They said: “I would be terrified if I had to face a DWP officer in my GP surgery, or worse, during an inpatient admission under the Mental Health Act.

The thought of anyone being in that situation when they need care, not pressure to discuss work, is horrifying.

Health professionals should protect lives, not enable harm.”

A spokesperson for the British Psychological Society said: “There is no connection between the awarding of the Department for Work and Pensions (DWP) contract and the British Psychological Society’s (BPS) stance on the government’s roll-out of work advisers in GP surgeries.

The BPS is an independent professional membership body, and our positions are shaped by our members, the best available evidence, and our ethical standards as set out in our charter.

Contract negotiations between the DWP and BPS remain ongoing and as such it would be inappropriate for us to comment further.

The BPS retains editorial and public independence and will continue to raise awareness where psychological evidence calls for challenge.”

There has been controversy for nearly a decade over DWP’s attempts to blur the lines between the health and employment systems by embedding work advisers in surgeries.

In March 2016, the Mental Health Resistance Network organised a protest about a year-long DWP pilot scheme which saw private sector job coaches placed in six GP surgeries in Islington, north London.

Denise McKenna, co-founder of MHRN, said at the time that the network would “never accept this scheme and we will never give up until it is abandoned”, and described it as a “drastic move” that would cause some people to stop seeing their GPs.

23 October 2025

 

 

Peers derail government plans to hand some DWP staff powers to use force against benefit claimants

Government plans under controversial new legislation to give some Department for Work and Pensions (DWP) staff “morally dubious” powers to use force against benefit claimants have been derailed by peers.

The public authorities (fraud, error and recovery) bill was set to give authorised DWP staff the same powers of search, entry and seizure as the police.

But unlike powers granted to the Public Sector Fraud Authority, the bill was also set to allow these officers to use “reasonable force” against benefit claimants when exercising their new powers.

Until now, one of the bill’s most controversial measures was that it is set to force banks to examine the accounts of claimants of means-tested benefits for potential breaches of benefit eligibility rules and then pass that information to DWP.

But a string of crossbench and opposition peers also raised concerns about the “reasonable force” measure on Tuesday during the bill’s report stage.

The crossbench hereditary peer Lord Vaux told the Lords: “This would make it lawful for a DWP officer – not a police officer, but a civil servant – to enter your home, seize your belongings and forcibly hold you down while doing so.”

He said this would be used against benefit recipients, a part of the population who are more likely to be disabled and are “more vulnerable” than the general population.

He said: “The use of physical force marks a far more serious infringement than the powers of search, entry and seizure alone.”

He was supported by Conservative peer Lord [Mark] Harper, a former minister for disabled people, who urged ministers to “not give power to use reasonable force to people who are not trained to use it and do not have proper oversight”.

The Liberal Democrat peer Lord Palmer said that “any exercise of physical powers must surely rest with the police.

Are we going to train a new breed of DWP officers who have to be tough and able to act as police? It is quite nonsensical.”

Baroness [Claire] Fox, a non-affiliated peer and former Brexit Party MEP, added: “I do not want DWP civil servants, who might have been on a minor training course, to have that power. I think it is wrong.

For them to have that power of physical force aimed at people on benefits seems wholly wrong and morally dubious.”

The Conservative shadow work and pensions minister Viscount Younger – a former DWP minister – said the government had “yet to offer a convincing explanation of why DWP officials need this power at all”.

He said Conservatives were “deeply concerned” by the new powers being granted to DWP investigators through the bill, and said the measures raise “profound questions about the limits of state power and the safeguards that ought to accompany it”.

Work and pensions minister Baroness Sherlock accepted that the bill would give authorised and trained DWP officers powers to use reasonable force against individuals, but she told fellow peers that the intention was for them “to be able to use that against property, not against people”.

And she said the search, entry and seizure powers would only be used for “serious organised criminality” and “where the DWP has a reasonable belief that someone has intentionally committed sophisticated, often high-value fraud against the DWP” and not against “an average benefit claimant who has accidentally overclaimed by £20”.

She said the “intention is that reasonable force will be used only against things, not people”, which “will be made clear in guidance and training”, and that the powers “will enable DWP-authorised investigators to use reasonable force to access locked cabinets and digital devices once they are lawfully on a premises”.

She said the law would also require that any application to the courts for a warrant to access a property would have to include “information about any vulnerable individuals who may be present on the premises”.

But an amendment proposed by Lord Vaux to remove from the bill the power to use reasonable force against individuals was approved by peers by 212 votes to 144.

Among the disabled peers voting in favour of Lord Vaux’s amendment were Liberal Democrats Baroness [Celia] Thomas and Lord Addington, and Conservatives Lord [Kevin] Shinkwin and Lord [Chris] Holmes.

No Labour peers voted in favour of his amendment.

It is not yet clear whether DWP ministers will attempt to re-introduce these powers into the legislation before the bill becomes law.

A DWP spokesperson said this morning (Thursday): “The amendment is subject to parliamentary process and will be discussed in the house in the next stages of the bill.”

The bill is due to return to the Lords today for its third reading, before it returns to the Commons for discussion of amendments made by peers.

23 October 2025

 

 

Reeves refuses to apologise for repeating false claim that social security spending is spiralling

Chancellor Rachel Reeves has refused to withdraw a misleading and inaccurate statement that scapegoated disabled people and other benefit claimants for the country’s economic problems.

In an interview with Channel 4 News, Reeves repeated the false claim that welfare spending was spiralling out of control.

She told the programme: “We can’t get to the end of this parliamentary session and have done nothing, because if more and more of our money that we spend as a government is spent on welfare, you’ve got less for the NHS, you’ve got less for schools.”

It came as government sources briefed the Times newspaper that Reeves was intending to raise revenue from the Motability disabled people’s vehicle scheme by £1 billion a year in the budget by attacking its VAT and insurance premium tax exemptions (see separate story).

Disability News Service (DNS) told the Treasury this week that Reeves should be aware that her statement on “welfare” was highly misleading.

This is because figures from the Office for Budget Responsibility reported last autumn* that welfare spending was stable as a proportion of GDP, and that it was lower than it was in 2015-16.

DNS shared figures with the Treasury that showed that the share of GDP was predicted to be 11.1 per cent in 2024-25; the same in 2025-26 and 2026-27; to fall to 11.0 per cent in 2027-28 and 2028-29; and to rise to 11.1 per cent again in 2029-30.

The Treasury, Department for Work and Pensions, and political parties, including Labour and the Conservatives, have been repeatedly shown these figures by DNS, and yet senior figures across the parties continue to claim that spending on social security is “spiralling”.

Last week, the Financial Times agreed with months of reports and analysis from DNS, academics and disabled campaigners, and concluded: “Costs are not spiralling.

Projected total welfare payments, at around 11 per cent of national income a year, are lower than when David Cameron was prime minister even though there are more pensioners.”

Chris Giles, the paper’s economics commentator, added in his article: “The welfare system is far from perfect but it cannot be blamed for your taxes rising in November’s Budget.”

The Treasury this week refused to comment on why Reeves and fellow ministers repeatedly claim that social security spending is spiralling out of control when it is not, and whether she would apologise.

*Chapter five of OBR’s Economic and Fiscal Outlook – October 2024, chart 5.2, shows welfare spending as a percentage of GDP: https://obr.uk/efo/economic-and-fiscal-outlook-october-2024/

23 October 2025

 

 

Timms goes back on his word by refusing to provide crucial evidence of Access to Work cuts

The disability minister has gone back on his word by refusing to provide crucial information that would help expose a “perverse”, secret programme to restrict grants made by the Access to Work disability employment scheme.

Sir Stephen Timms told Disability News Service (DNS) at Labour’s annual conference late last month that he would provide the date on which he approved an order from senior civil servants for Access to Work (AtW) staff to be more “scrupulous” in how they applied guidance.

Now, three weeks on, he is refusing to reveal this date.

This will make it harder to secure the order through a freedom of information request.

Instead of responding to an email from DNS seeking the information, Sir Stephen forwarded the message to the Department for Work and Pensions (DWP) press office.

But DWP’s press office also failed to provide the information.

It said in a statement: “No changes have been made to Access to Work policy.”

Instead of providing the date of the order, it provided background information which failed to clarify when, or if, Sir Stephen approved a document about the guidance, but suggested that the changes were put into effect through additional training for AtW case managers.

The briefing did confirm that Sir Stephen had been made aware that this work was taking place.

The DWP press office had failed to clarify the information it provided by noon today (Thursday).

Last week, DNS reported how official government figures revealed the first signs that ministers had been engaged in a “perverse” programme to secretly restrict AtW grants.

The DWP figures showed that the number of people who had any AtW provision approved fell by more than 10 per cent in the year to March 2025.

The figures also showed that the number of disabled people who had AtW requests for aids and equipment approved plunged by 16 per cent on the previous year, while approvals for support for travel to work fell by 14 per cent, and the number of approvals for mental health support dropped by seven per cent.

Figures from the last six months – not due to be published for another 12 months – will eventually show how the cuts to essential funding are “far more severe” than those shown in last week’s DWP figures, one disabled expert has predicted.

In the interview at the Labour conference in Liverpool last month, Sir Stephen admitted that he had seen a submission, which he had approved, which stated that AtW guidance would now be “scrupulously applied”.

He said he could not remember when he saw the submission, but his special adviser told DNS: “I think we need to check.”

Sir Stephen then said he would check in DWP records when this took place, and he added later in the conversation: “But what I can check, John*, is when this happened.”

*DNS editor John Pring

23 October 2025

 

 

Disabled people describe impact of ‘very unfair’ extra costs caused by DWP’s universal credit migration

Disabled people have described their anger with the Department for Work and Pensions (DWP) for failing to warn them of the significant hidden costs – which can be more than £2,400 a year – of transferring onto universal credit from their old “legacy” benefits.

They have come forward to share how the unexpected hit to their finances caused by moving onto universal credit from employment and support allowance (ESA) has impacted their ability to cope with the cost-of-living crisis.

They are facing extra costs from their local authority as a result of the move, even though DWP has previously insisted that they would – at least initially – be no worse off on universal credit than on their previous benefits once they were forced onto the new system through the “migration” process.

But Disabled People Against Cuts (DPAC) revealed last week that it had been hearing from disabled people who have been hit hard in two different ways by this process.

Some disabled people have seen their care charges to their local council increase, sometimes by more than £50 a week.

Other disabled people are receiving a much lower discount under their local council tax reduction scheme after migrating onto universal credit.

DPAC said this week that disabled people had continued to come forward to describe the extra costs they were facing, which appear to vary across the country.

DPAC is hoping a legal action might be possible, and it is still looking for disabled people who are eligible for legal aid and might be willing to take a legal challenge with DPAC’s support.

It also encouraged those affected to complain to their MPs, and to continue to share their stories with DPAC.

Linda Burnip, DPAC’s co-founder, said: “Many people are losing over £200 a month which is more than £2,400 a year from already meagre social security payments and that has to be wrong.

DPAC demand DWP explain what it knew and when about this added cost to the migration process.”

This week, disabled people have described to Disability News Service (DNS) the impact of the unexpected costs of migrating to universal credit from ESA.

Mark Catlin, from Hertfordshire, is now having to pay £30 a month in council tax – rather than nothing – after he was moved onto universal credit from ESA in May this year.

He assumed it was a mistake when he received the bill but when he called the council he was told that the council tax reduction for those on ESA was 100 per cent but was just 75 per cent if the same person moved to universal credit.

Catlin told DNS it was “not easy” to cope with the extra monthly cost.

He said he believed DWP did not care about the extra payments, and that most of its advisors were “not even aware of these changes; if they are, they’re not making people aware of them”.

And he said he was “pretty disgusted” with the council.

He said: “I don’t understand how they can justify the reduction change just because the name of the benefit changes, when there’s been no change in financial entitlement, especially with the cost of living being so changeable.”

Another disabled claimant, Lisa, from Plymouth, moved onto universal credit in June.

She told DNS: “I heard all the government statements saying those moving from legacy benefits would have their entitlement protected and income would stay the same.”

But she found out that the change meant her council expected her to pay 40 per cent of council tax charges, rather than the previous level of 20 per cent, which means an extra £41 a month.

Lisa, who has long-term health conditions, said the extra charge was “very unfair”.

She said: “It’s becoming more difficult to cover expenses and costs to just pay bills and food each month.

It has become clear the DWP and government ministers have wiped their hands of any responsibility of this extra charge, saying it’s up to the individual councils what rates they set their council tax levels at.”

Labour’s Debbie Abrahams, who chairs the Commons work and pensions committee, was not available to comment on the concerns this week.

Meanwhile, DWP has again refused to say if and when it became aware of the issue, whether it was concerned, or if it would take any action.

Last week, it issued the following statement: “We support millions of people through universal credit every year – including those who have moved from ESA – and it’s a top priority for us to ensure that people receive the help they are entitled to.”

23 October 2025

 

 

Ministers’ refusal to raise limit on accessible housing grants is discriminatory, secret reports admits

The continuing refusal of ministers to raise the upper limit on a scheme that helps disabled people make access improvements to their homes is discriminating against some of those with higher support needs, a secret government report has admitted.

The internal review into how the upper limit on disabled facilities grants (DFG) is working was obtained by Disability News Service (DNS) through a freedom of information request, after care minister Stephen Kinnock refused to publish it.

The DFG scheme helps councils in England fund access improvements to disabled people’s homes, but the upper limit of £30,000 was set in 2008.

Councils have a legal duty to provide adaptations for disabled people, subject to a needs assessment, eligibility criteria and a means test, and can also provide funding above the upper limit at their own discretion.

Adaptations can include stair-lifts, level access showers, widening doors, ramps, grab rails, raised toilets, access to gardens, height-adjusted kitchens, heating systems, loft conversions and home extensions.

Seven years ago, an independent review commissioned by the government recommended increasing the limit in line with inflation, and introducing regional variations.

Last year, shortly before the general election, a report by the cross-party levelling up, housing and communities committee highlighted “many shortcomings” in the DFG system, and called on ministers to review the £30,000 upper limit and set new regional upper limits which took account of inflation and construction costs.

Now an equality impact assessment carried out as part of a secret internal review has found that the upper limit of £30,000 is “likely to be adversely impacting small numbers of disabled people in some groups, including children with complex needs and working-age adults”.

It also found that disabled people of all ages “with severe conditions such as multiple sclerosis, Parkinson’s disease or those suffering from acquired brain injuries are also disproportionately negatively impacted by the current upper limit”.

It found that disabled people affected by the upper limit can see vital adaptations delayed as they seek additional funds for the work, “or in the worst cases, the adaptations are not provided”, which can have a “significant detrimental impact on disabled people and their families”.

But it concluded that this discrimination was “proportionate to achieving the aims of the upper limit” because it allowed councils to manage their DFG budgets and support “the majority of eligible individuals to receive an adaptation”.

The secret report added: “In reality, given the benefits of having an upper limit, it [is] unlikely that the DFG will ever be a suitable means of funding the entirety of high cost adaptations.

There is always likely to be some impact on that high cost cohort, which is always likely to require some additional funding from alternative sources.”

The report concluded that ministers needed to “continually keep the policy under review and improve our evidence and analysis”, particularly to fill “evidence gaps” on disabled people who have “dropped out of applying for a DFG or experienced delays because of the upper limit”.

It also concluded that there were “clear benefits for keeping an upper limit in place” because it “provides a mechanism that helps ensure proper conversations are held about alternatives to adapting the home, and to control costs”.

But it said the government should decide “whether the current level of the upper limit is still appropriate and whether it should be raised”.

Mikey Erhardt, policy lead for Disability Rights UK, said: “The continued refusal of successive governments to raise the upper limit is as frustrating as it is counterproductive.

Given the state of local authority finances, meaning top-up payments are unlikely, disabled people with the highest needs, whose lives could be changed by adaptations, will likely not get the changes they need to live safely in their own homes.

The government’s continued housing policy of prioritising the needs of developers, private landlords, and big business necessitates the continued use of systems like the disabled facilities grant.

Simply put – there are no accessible homes, and those actors have no intention to build them, so we need DFG to create them.

This report makes clear the goals of the government: short-term cost saving and cost saving alone.

The report makes clear the dangers of not raising the DFG ceiling.

We are calling on the government to do the right thing and raise the ceiling and link it to inflation so no more disabled people have to live in dangerous, inaccessible homes.”

Svetlana Kotova, director of campaigns and justice at Inclusion London, also criticised the government for failing to increase the upper limit.

She pointed to Inclusion London’s Barriers at Home report, which found earlier this year that one in three people with mobility impairments do not have level access in their own homes.

She said the government’s failure to raise accessibility standards on new homes and its failure to increase the upper limit on DFGs meant that “new, inaccessible homes will be built, and the adaptations we need won’t be fully funded”.

She said: “It is a scandal that in our country, disabled and older people now have to fundraise to ensure they can access the bathroom, bedroom or get out of the house.

The government can change this: make sure everyone who needs adaptations can get them, and raise minimum accessibility standards for new homes, so that 10 per cent meet the M4(3) wheelchair-user standard, and the rest meet the M4(2) accessible and adaptable standard.”

The government’s internal review found that most DFGs above the upper limit went to working-age adults (40 per cent) and disabled children (43 per cent), according to reports by councils from 2023-24, with older people receiving another 16 per cent.

The average cost of a high-value adaptation ranged from £47,206 in the north-east of England to £56,685 in the south-west.

The most expensive DFG to be reported by local authorities cost £159,000.

The average cost of a DFG in 2023-24 was about £10,000.

Landlords, the NHS and social services rarely contribute to higher-cost adaptations, so any additional funding must usually come from either the local authority or the disabled occupant.

Most councils told the government that their current budget was either not big enough to meet demand for DFGs, or that they would need to reduce their discretionary grants if budgets do not increase in the future.

DNS requested a copy of the internal review from the Department of Health and Social Care (DHSC) after care minister Stephen Kinnock told Liberal Democrat MP David Chadwick last month that the report would not be published.

Last October’s budget saw an £86 million increase in central government spending on DFGs, which was set to reach £711 million in 2025-26.

DHSC and the Ministry of Housing, Communities and Local Government (MHCLG) share responsibility for DFG policy.

They agreed to review the upper limit after a judicial review claim challenged its legality.

DHSC had failed to comment on the internal review by noon today (Thursday).

23 October 2025

 

 

Ministers finally announce progress on ‘liberty safeguards’, but also challenge vital definition

The government is set to push ahead with a long-delayed new system of safeguards that could have a significant impact on service-users who are unable to consent to restrictions placed on their liberty in health or social care settings.

There have been years of delays to the introduction of Liberty Protection Safeguards (LPS), which will replace the current Deprivation of Liberty Safeguards (DoLS) in England and Wales.

But care minister Stephen Kinnock finally announced this week that there will be a new consultation on the new LPS system “in the first half of next year”.

The announcement came as the Supreme Court this week heard a case brought by the Northern Ireland attorney general, which is examining the definition of “deprivation of liberty”.

The case challenges two 2014 rulings by the Supreme Court – one of which became known as the Cheshire West ruling – which significantly widened the definition of who would be protected by the DoLS system.

The Cheshire West ruling found that a disabled person was being deprived of their liberty if they were obliged to live in a particular place “under continuous supervision and control”, and they were not free to leave their homes or move away without permission, and they could not consent to decisions about their welfare.

It also found that such people needed “a periodic independent check on whether the arrangements made for them are in their best interests”.

But the Department of Health and Social Care has been heavily criticised for intervening in this week’s case and for asking the Supreme Court to set aside the Cheshire West ruling.

The 2014 rulings led to an increase in referrals from 13,700 in 2013-14 to 322,455 in 2023-24 and a backlog of 123,790 cases.

The rulings eventually led to the drawing up of the LPS system, based on a report by the Law Commission.

The last government had originally planned to bring in LPS in October 2020, but its implementation was repeatedly delayed by Conservative ministers.

The Department of Health and Social Care said this week that the new system would “deliver improved protection and an easier and improved system”.

It said the current DoLS system was “bureaucratic and complex” and led to “poor understanding and application of the law by professionals, unacceptable distress for families” and the lengthy backlog, which placed pressure on the social care system.

Kieran Lewis, rights and migration policy manager at National Survivor User Network (NSUN), said: “We urge the Department of Health and Social Care and the Ministry of Justice to treat their consultation on the Liberty Protection Safeguards with the care it deserves, making it genuinely accessible and actively seeking out people subject to deprivations of liberty, as well as their families and carers, to shape it.

We also echo calls to defend the Cheshire West judgement and ensure that any changes in the law around deprivation of freedom are made in close collaboration with disabled people and their organisations.

This is the bare minimum, considering the complete lack of trust that disabled people now have in this government, which continues to demonstrate its lack of real concern for them.”

Kinnock said the consultation was about “fixing a broken system by hearing directly from those with lived experience and their families”.

He said: “There is currently a shameful backlog in the system of unprocessed cases under the current system which means that people’s rights are not being protected.

At the same time, we know that many people in the system and their families find these intrusive assessments distressing.

This is about ensuring we are fully focused on the most vulnerable people in our society and their families – understanding their needs, ending the maze of referrals and paperwork, and delivering the best protections and safeguards possible.”

The responses from next year’s consultation will inform a new code of practice to the 2005 Mental Capacity Act, which will be laid before parliament.

23 October 2025

 

 

Other disability-related stories covered by mainstream media this week

Families with children left disabled by long Covid have told a national inquiry “it’s almost as if we don’t exist”. Thousands of children have been left disabled and often bedbound due to the post-viral syndrome which their parents say much of the NHS still refuses to recognise. They told the Mirror of their shock at discovering from the UK Covid-19 Inquiry that medics were told during the pandemic not to “label” children with long Covid – meaning thousands have never been properly diagnosed: https://www.mirror.co.uk/news/uk-news/covid-19-inquiry-reveals-forgotten-36115749

Placing debt and benefits advisers in GP surgeries could ease pressure on the NHS and improve patients’ health across the country, a pilot scheme has shown. The Financial Shield project, run across 34 GP practices in south London, found that more than half of participants reported improvements in their physical or mental health after receiving tailored financial support, with around one in three saying they needed fewer GP appointments afterwards. The scheme has government backing: https://archive.ph/tbQWL

Teachers, not councils, will take a greater role in assessing children with special educational needs and disabilities, the education secretary has revealed in an interview with The i Paper. Bridget Phillipson insisted that “formal assessment processes” would still take place but signalled plans to shift responsibility from local authorities to schools and teachers as she seeks to bring in higher overall standards of support in mainstream schools: https://archive.ph/AKoZj

Long-awaited plans to overhaul the crisis-hit special educational needs and disabilities system have been delayed. The schools white paper had been due to be published this autumn but will now be released next year. The decision is understood to have been made extremely recently, with education secretary Bridget Phillipson having given a speech on the white paper just last week: https://www.mirror.co.uk/news/politics/long-awaited-send-plans-delayed-36116454

Decades of efforts by mainstream politicians to roll back welfare programmes have given rise to an “extremely dangerous” discourse that has helped fuel the rise of the far right and right-wing populists in countries around the world, a top UN expert has told the Guardian: https://www.theguardian.com/world/2025/oct/21/welfare-cuts-have-fuelled-rise-of-far-right-and-populism-top-un-expert-says

One in 12 secondary pupils report being put into school isolation rooms at least once a week where they often spend in excess of eight hours, missing more than a full day of lessons, according to research. Children with special educational needs were more than twice as likely to be placed in isolation, otherwise known as internal exclusion, while students from low-income backgrounds were also disproportionately affected: https://www.theguardian.com/education/2025/oct/23/one-in-12-secondary-pupils-put-in-isolation-rooms-at-least-once-a-week-study-finds

An autistic man who volunteered for four years at Waitrose has lost his role after his mum asked if he could be paid. Tom Boyd stacked shelves and emptied stock cages at a branch in Cheadle Hulme, Greater Manchester, while being accompanied by a support worker. He began in 2021 and has now racked up more than 600 hours of volunteering: https://www.mirror.co.uk/news/uk-news/waitrose-sacks-autistic-volunteer-after-36106706

23 October 2025

 

News provided by John Pring at www.disabilitynewsservice.com

Oct 222025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
The words "We want an Independent PIP Review" in bold and black text, with Independent highlighted in red. On the left there is a tear-out effect of a greyscale photo of a disability protest, and a red-tinted photo of Stephen Timms, the disability minister.
Disability campaign group Disabled People Against the Cuts Cymru pose for a group photo outside the Senedd (Welsh parliament) with Sioned Williams MS. Sioned is holding up the DPAC Cymru letter. There are 15 people in the photo. Two people are wearing DPAC t-shirts. Four people are using wheelchairs. Two people are wearing face-masks. One person is holding a flag showing a Welsh dragon with a disability equality colour background. Behind everyone is the DPAC Cymru banner. It is very large, and has five people holding it. It says Disabled People Against Cuts and then the word Cymru with a Welsh dragon background effect on the text. It has the DPAC logo which is a red, green, purple, blue wheel being held by four arms with different skin tones. At the center of the logo is an upside-down black triangle bearing the letters D P A C and the word Cymru. Behind the campaigners are various tall buildings in Cardiff. The nearest building is made of a striking orange brick.

On Tuesday 14th October, members and supporters of Disabled People Against Cuts Cymru (DPAC Cymru) met outside the Senedd (the Welsh Parliament) to protest the disability cuts and hand over a letter to Senedd members. The letter, co-signed by over 700 individuals and organisations, outlined DPAC’s request to the Welsh Government to support an independent review of Personal Independence Payment (PIP). The letter calls for a PIP review that is truly led independently by disabled people and our organisations, to allow our lived experience to influence the policies and decisions that will ultimately affect us.

We are grateful to the members of the Senedd who met with us or wrote to us about this matter, and we hope that all members will take into consideration what the letter said.

The lobby happened on the same day that the Minister for Social Security and Disability, Sir Stephen Timms, declined an invitation to meet with the Senedd Cross Party Group on Disability due to “diary pressures”. Timms is currently responsible for the PIP review, and we feel that his response highlights how disabled people and Disabled People’s Organisations (DPOs) are being excluded from the review and decision-making process.

Timms’ promise that the PIP review would be a genuine co-production with disabled people is not being upheld, and the Senedd lobby was part of an ongoing campaign to ensure that disabled people’s voices are being heard.

As a new member of DPAC Cymru, it was wonderful to see so many people at the Senedd to support what DPAC is working to achieve. Given the current situation, it is vital that disabled people’s voices are amplified in a way that is accessible, impactful, and authentic. We will continue to campaign for the rights of disabled people and to push for a fairer, independent PIP review to create a system that truly supports the needs of disabled people across the UK.

Briallen Symons-East
Disabled People Against Cuts Cymru (DPAC Cymru)

 

Disability campaign group Disabled People Against the Cuts Cymru pose for a group photo outside the Senedd (Welsh parliament) with Sioned Williams MS. Sioned is holding up the DPAC Cymru letter. There are 15 people in the photo. Two people are wearing DPAC t-shirts. Four people are using wheelchairs. Two people are wearing face-masks. One person is holding a flag showing a Welsh dragon with a disability equality colour background. Behind everyone is the DPAC Cymru banner. It is very large, and has five people holding it. It says Disabled People Against Cuts and then the word Cymru with a Welsh dragon background effect on the text. It has the DPAC logo which is a red, green, purple, blue wheel being held by four arms with different skin tones. At the center of the logo is an upside-down black triangle bearing the letters D P A C and the word Cymru. Behind the campaigners are various tall buildings in Cardiff. The nearest building is made of a striking orange brick.

Photo: Disability campaigners from Disabled People Against Cuts Cymru outside the Senedd in Cardiff.

 

A photo of a disability lobby at the Senedd (Welsh parliament). Lee Ellery, who is a wheelchair user, is handing over pack of documents to the Welsh politician Sioned Williams. Lee is smiling and in the middle of talking. In the background is the Disabled People Against Cuts Cymru (DPAC Cymru) banner.

Photo: Lee Ellery hands a pack of documents to Sioned Williams MS.

 

Sioned Williams MS talks to campaigners from Disabled People Against Cuts Cymru (DPAC Cymru) outside the Senedd. There are about 20 people in shot. Four people are users of powered wheelchairs. One person is wearing a yellow medical face mask and is draped in a Welsh flag with disability equality colours. Another wears a black medical face mask. People are standing around chatting, while Sioned is at the center of the photo. At the right of the photo is the DPAC Cymru banner being held by several people. The banner says "rights not charity." One person wears a hat that says PCS. One has a copy of the Socialist newspaper.

Photo: Lee Ellery hands a pack of documents to Sioned Williams MS – from another angle!

 

Disability campaigners from Disabled People Against Cuts Cymru at the Senedd (Welsh Parliament) talk with the politician Jenny Rathbone MS.

Photo: DPAC Cymru talk with Jenny Rathbone MS outside the Senedd.

 

Disability campaigners Lee Ellery and Joshua Reeves, who are both wheelchair-users, are conversing. Around them are other campaigners from Disabled People Against Cuts Cymru.

Photo: Disability campaigners Lee Ellery and Joshua Reeves BEM conversing.

 

Lee Ellery, Ben Golightly, John Williams from Disabled People Against Cuts Cymru are talking to Sioned Williams MS. In the background is the Senedd building. Lee is using a powered wheelchair. He is wearing smart clothes. Sioned is holding a pack of documents and smiling and looking at Lee attentively. Ben is wearing a DPAC t-shirt and is holding a small placard with text. John is holding a copy of the Socialist newspaper and looking at Ben.

Photo: disability campaigners converse with Sioned Williams MS.

 

Darren Millar MS and staff converse with disability campaigners outside the Senedd. In the background are trees and the sea. It is picturesque, although overcast.

Photo: DPAC Cymru spoke with Darren Millar MS and his staff outside the Senedd.

 

Lee Ellery and Ben Golightly from Disabled People Against Cuts Cymru (DPAC Cymru) pose for a photo with Sioned Williams. Lee Ellery is a wheelchair user and is in smart clothes. Ben is wearing a DPAC t-shirt. Ben is holding a sheet of paper with the DPAC Cymru logo that says "No disability cuts! Disabled people want to run our own independent PIP review!" Sioned is holding a sheet of paper with the same message translated into Welsh. She is also holding up the DPAC Cymru letter with 700 signatures. In the background, John Williams is standing to their leftwith a copy of a newspaper called the Socialist. On the cover of the newspaper, it says: "Your party: let's build a party to fight labour's war and austerity. defend the right to protest."

Photo: We posed for photos with Sioned Williams MS holding bilingual (English and Welsh) signs that said:
“No disability cuts! Disabled people want to run our own independent PIP review!”

Oct 092025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Tory trio mislead party conference on disability benefits as they stir up hostility towards disabled claimants 1

Government ‘has lost its way’ on accessible housing, after new towns report ignores disabled people 3

Alarm over government’s choices to lead ‘over-diagnosis’ review that could help ministers cut benefits 5

Coach firm to pay thousands to accessible transport activist after driver lied that he threatened violence 8

Access to Work dossier of evidence shows ‘real harm’ and job losses caused by DWP cuts and failings 10

Greens show contrast with other major parties on disability cuts and refusal to stir up hostility to claimants 13

New film celebrates 10 years since ‘moment in time’ victory over care charges in London borough 14

Other disability-related stories covered by mainstream media this week 16

 

 

Tory trio mislead party conference on disability benefits as they stir up hostility towards disabled claimants

A trio of leading Tories have used misleading and offensive statements at their annual conference in Manchester to scapegoat disabled people who rely on support from the benefits system and whip up hostility towards them.

The Conservative party made it clear this week that it would go further and faster than the Labour government in cutting disability benefits, and said it would cut £23 billion from social security spending if it won back power.

Some of these savings would be used to pay for the abolition of stamp duty on residential property sales*, which would only benefit the better-off.

The most offensive line may have come from Tory leader Kemi Badenoch, who told the conference yesterday (Wednesday): “I stand for a society where… the vulnerable are supported, but where freeloaders are told where to get off.”

She said a Conservative government would “restrict benefits to those with more severe mental health conditions, not anxiety or mild depression”**.

Disability News Service (DNS) reminded the party this week how government-funded research found that when a Conservative-led government tried to slash the number of people on out-of-work disability benefits and force them into work in the post-2010 austerity years, it led to 590 suicides in three years.

The party had not responded to these concerns by 11am today (Thursday).

Badenoch also told the conference that “after Covid, 2,000 people a day were being signed onto out-of-work sickness benefits”, which she said was “a national tragedy”.

There was no suggestion in the former engineer’s speech that she had connected the impact of a deadly and disabling pandemic with this increase in the number of people being unable to work due to sickness or disability.

Badenoch also appeared to suggest that she supported allowing disability hate speech to pass unpunished, telling Tory members: “I stand for a society where free speech trumps hurt feelings.”

Mel Stride, the former work and pensions secretary and now his party’s shadow chancellor, had spoken earlier in the week of the “spiralling welfare bill”.

DNS has now told the party’s press office on at least three occasions that figures from the Office for Budget Responsibility*** show clearly that social security spending as a proportion of GDP**** is predicted to remain at or close to 11.1 per cent for the next five years, and that it is lower than it was in 2015-16.

Again, the party had not responded to these concerns about Stride’s misleading comment by 11am today.

The party also announced plans to prevent anyone other than British citizens from receiving social security support, if it regains power.

It appears that this would apply to disabled people with significant support needs and those who have legally worked in the country for years through “indefinite leave to remain”.

The third shadow minister to mislead the conference on cuts to disability benefits was shadow work and pensions secretary Helen Whately.

She told Tory members: “Millions are getting benefits for anxiety and ADHD, along with a free Motability car.”

A disabled person can only qualify to join the Motability scheme if they receive the enhanced mobility component of personal independence payment (PIP) or similar benefits.

In fact, DWP figures showas highlighted by the Benefits and Work website – that only about 190,000 PIP claimants have ADD, ADHD, anxiety or anxiety-related conditions as their “main disabling condition” and receive an enhanced mobility component.

And many of this group will not have exchanged their PIP mobility component for a Motability vehicle.

It is possible that Whately was referring to all those disabled people with anxiety and ADHD who have a Motability vehicle (ie including those with a different main disabling condition in addition to a mental health condition or being neurodivergent), but – if so – her statement was still highly misleading.

And even if that had been her intention, Motability Operations, the company that runs the scheme, says it has only a total of 860,000 customers, and many of those use their allowance to hire a powered wheelchair or mobility scooter.

Whately’s comments also suggest that PIP claimants receive a “free” car in addition to that benefit, when in fact a claimant usually has to exchange all their mobility allowance to lease a Motability vehicle, and must also often make a non-refundable advance payment.

Once again, the Conservative party had refused to comment by 11am today on Whately’s figures.

*It is believed this would apply to primary residences in England and Northern Ireland

**Although she said she wanted to “restrict benefits”, it is unlikely that she meant that people with anxiety or “mild” depression would be prevented from accessing mainstream benefits such as the standard universal credit allowance

***See chapter five of OBR’s Economic and Fiscal Outlook – October 2024, chart 5.2

****Gross domestic product, the size of the country’s economy in a particular year

9 October 2025

 

 

Government ‘has lost its way’ on accessible housing, after new towns report ignores disabled people

The government has been accused of losing its way on accessible housing, after refusing to explain why a report by its “taskforce” on delivering a series of new towns across England does not include a single mention of disabled people.

The independent report – commissioned by the government – recommends 12 potential locations for new towns across England, with at least 10,000 new homes in each location.

But the 135-page report contains only two brief references to the need for accessibility, either with the new homes themselves or the built environment surrounding them, and there is no mention of working-age disabled people.

One reference in the report says new towns should “include homes for older people, as well as specialist housing built to accessible and adaptable standards”.

The other says the mix of homes in new towns should include “homes for market sale, private rent, affordable housing, and specialist accommodation for students, families, and older people, all within a single coherent masterplan”.

Disabled people’s organisations that have been campaigning for action to solve the accessible housing crisis were critical of the latest failure by the Ministry of Housing, Communities and Local Government (MHCLG).

Mikey Erhardt, policy lead for Disability Rights UK, said: “It is unacceptable that, in 2025, a plan to deliver thousands of new homes, to tackle the housing crisis, will do nothing to improve the lives of disabled people.

Relegating the needs of millions to a classification as ‘specialist’ shows just how entrenched ableist views are within the department.

What is specialist about creating places that millions can actually call home, instead of the less than 10 per cent that disabled people can currently even visit?

Yet again, we see a government department that has lost its way in trying to triangulate policy in favour of big developers and landlords, with disabled people as ever missing out.

Talk about a missed opportunity; they’ve not even chosen to commit to a minimum number of accessible or wheelchair-accessible homes, let alone ensuring DDPOs* are included in the planning process.

If our newest towns can’t be accessible, which ones will be?”

Last week, housing secretary Steve Reed announced that the government would build 12 of the new towns across England, but he and his party failed to make any pledge that accessibility would be central to their design.

More than 15 months after the general election, disabled people are still waiting for the new government to say whether it will introduce stricter minimum accessibility standards for new-build homes in England, three years after a pledge by the last Conservative government – which was never fulfilled – to take action to address the critical shortage of accessible housing.

Laura Vicinanza, senior policy and stakeholder engagement manager for Inclusion London, said: “The taskforce talks about accessible ‘specialist housing’, but accessible and adaptable standards must apply to all housing, so we’re not cut off from our communities.

Housing with a baseline level of accessibility benefits us all – it allows us to stay in our homes longer as our needs change and we age.

Three years ago, the Conservative government committed to raise the minimum accessibility standards for all new-build housing to the M4(2) accessible and adaptable standard, but they didn’t follow through.

It’s time for Labour to commit to M4(2) accessibility for all new-builds, and for 10 per cent of new housing to be M4(3) wheelchair-accessible, focused in social housing.

This is the opportunity to ensure that this wave of new housing and new towns doesn’t lock us out of safe housing for another generation.”

This week, Disability News Service (DNS) asked the government why the taskforce and its report had almost completely ignored disabled people’s housing needs, and the opportunity to build in accessibility across the new towns from the beginning; and why there was nothing in the taskforce report that sets a minimum level of accessible homes, including how many wheelchair-accessible homes should be built in the new towns.

DNS also asked for reassurance for disabled people that the government’s new towns plans would build in accessibility right from the start and from the ground-up, in co-production with disabled people and their user-led organisations.

MHCLG declined to explain why the taskforce report contained so few references to accessible housing and built environment in the new towns and failed to mention disabled people.

And it once again said it would set out its policies on accessible new-build housing shortly.

At last year’s Labour party conference, in September 2024, after DNS questioned the party on the failure of ministers to mention the accessible housing crisis, a Labour spokesperson promised the government would “set out its policies on accessible new build housing shortly”.

An MHCLG spokesperson said in a statement this week: “Everyone deserves to live in a decent home that is suitable for them and meets their needs.

We will create New Towns that work for everyone, including disabled people, and we welcome recommendations from the taskforce that they should include specialist housing built to accessible and adaptable standards.

We’re committed to working with disabled people and their organisations to shape these new communities together.”

*Deaf and disabled people’s organisations

9 October 2025

 

 

Alarm over government’s choices to lead ‘over-diagnosis’ review that could help ministers cut benefits

The government’s decision to commission a review of alleged “over-diagnosis” of mental health conditions and neurodivergence has caused alarm among many disabled people, with fears that it will allow ministers to justify further sweeping cuts to disability benefits.

There is also concern that health and social care secretary Wes Streeting has commissioned two high-profile mental health figures with controversial backgrounds to lead the review.

Although the government has not yet confirmed the review will take place, it will reportedly examine the prevalence of mental illness and neurodivergence, “with a particular focus on whether some conditions are being overdiagnosed”.

But disabled activists believe its authors have been chosen because they will “help to slash the social security bill”.

The review will apparently be chaired by Professor Peter Fonagy, while the vice-chair will be Professor Sir Simon Wessely.

Fonagy is a highly-decorated clinical psychologist and psychoanalyst but he has also been closely associated with the Serenity Integrated Mentoring (SIM) programme, which was described as unethical, unlawful and unsafe and “a national scandal” that had put people in severe mental distress at risk of being denied vital support.

He was lead author of an article (PDF) whose co-authors included Paul Jennings, the former police officer who founded SIM, and which examined how SIM was working in London and concluded six years ago that it was “promising”.

Jennings described Fonagy in one presentation as a “senior supporter” of the programme.

Campaigning by the StopSIM Coalition later exposed SIM as discriminatory, coercive and punitive, and eventually persuaded NHS England to admit it was wrong to endorse SIM without applying “sufficient scrutiny” and to accept that this had harmed service-users.

Wessely’s appointment is likely to prove even more divisive.

He helped recruit patients onto the notorious, and later discredited, PACE trial – part-funded by the Department for Work and Pensions – and he was hugely supportive of the PACE research (PDF) into the use of controversial treatments such as cognitive behaviour therapy and graded exercise therapy for those with ME.

In 1993 (PDF, page 17)*, Wessely had written to the then Department of Social Security to argue that the only difference between “chronic fatigue syndrome, or ME as it is sometimes known” and “the major psychiatric disorders” was “the existence of a powerful lobby group that dislikes any association with psychiatry”.

Wessely argued in his letter that any suggestion that ME was a neurological condition would “discourage any sensible efforts at rehabilitation” and lead to an “ever increasing stream of claims for permanent benefits in people who might otherwise have had a chance of recovery”.

The view – shared by Wessely – that it was the attitudes of people with ME that were preventing their recovery, and the impact of this belief among many doctors and scientists on the treatment of many thousands of people with ME, was described by the Guardian’s George Monbiot last year as “the greatest medical scandal of the 21st century”.

Wessely also led a review of the Mental Health Act, which was criticised for falling “significantly short” of recommending full human rights for people in mental distress, but was a blueprint for Labour’s much-criticised mental health bill.

Although the Fonagy review has yet to be officially confirmed by the Department of Health and Social Care (DHSC), its existence was revealed by the well-connected Health Service Journal (HSJ).

Linda Burnip, co-founder of Disabled People Against Cuts (DPAC), said: “I think the choice of these two people shows how little regard the government, and Streeting and Timms** in particular, have for the fears of disabled people.

It seems likely that they have deliberately been chosen to help to slash the social security bill.”

The grassroots, user-led mental health group Recovery in the Bin (RiTB) said both appointments were “safe establishment” figures with troubling backgrounds, such as Wessely’s links to the ME “forced exercise programmes” and Fonagy’s links to SIM, which suggested “a very low probability that this will be an open and fair investigation”.

RiTB said: “We expect it will return findings the government will find useful to deny people benefits.

The issue that should be investigated is the thousands of deaths covered up by the DWP.

Instead, they want to cause more death.”

A spokesperson for DPAC Cymru said it was “alarmed” at the decision to appoint Fonagy and Wessely, whose backgrounds were “a clear signal” of a “politically-motivated review that has had its outcome decided in advance.

In the context of an NHS starved of funding, disability welfare cuts, and the UK government’s demonisation of disabled people, it is obvious why these two men have been selected.”

A DPAC Cymru member added: “Normalising mental health and neurodiversity normalises seeking help and clarity which makes diagnosis more accessible.

We’ve always existed, we’ve always been different, we just didn’t have the ability to seek help or diagnosis.

This whole ‘autism is new’ and ‘over-diagnosed’ argument is just another load of rubbish to demonise young people, make disability a taboo, exclude disabled communities, and save rich people pennies on providing help to people who really need it, and it frustrates me so incredibly much.”

Bethan Edwards, co-founder of the Stop SIM Coalition, which has now been disbanded, told Disability News Service (DNS) this week: “Professor Fonagy led an evaluation of SIM during its implementation in London in 2018 and 2019. 

SIM involved withholding care from people in extreme mental distress and involved the threat of criminalisation for attempting to use statutory services to meet significant mental health needs. 

It should not have taken a group of service-users to bring this to the public and professional bodies’ attention in 2021, leading to SIM’s demise. 

The alarm could and should have been raised sooner, including by Professor Fonagy himself. 

I, therefore, have very little confidence that the DHSC’s review will put the well-being and safety of people with mental health needs ahead of the Labour governments agenda – to cut welfare spending and to continue underfunding mental health services.”

And Kate Skinner, a neurodivergent campaigner, psychology student and academic research assistant, told DNS: “In my mind, the government’s potential reasons behind this review are straightforward: if fewer people qualify for diagnostic labels (such as ADHD), then fewer people will qualify for benefits, accommodations, and specialist services, as so many places lock the provision of support behind these labels.

Reviews like this one feel like their real purpose is redefining who counts as being ‘deserving’ of support, as evidenced by the wider media, which has been chipping away at the ‘validity’ and ‘deservingness’ of neurodivergence for a while now.”

She said: “I understand why many disabled people, particularly those who are neurodivergent, are deeply concerned about this review.

Psychology and psychiatry have a long history of researchers deciding what is ‘best’ for others, while ignoring the lived experiences of the people they study.

This history of exclusion and paternalism already makes it difficult to trust that this new review, commissioned in such a negative light, will be conducted with genuine openness or ethical integrity.”

Skinner added: “One of the professionals leading this review [Wessely] has previously argued that greater awareness of mental health conditions may not be ‘beneficial’, and has warned against ‘over-professionalising’ or ‘medicalising’ certain conditions.

Therefore, it is difficult not to feel that the government is seeking to use ‘experts’ to push through a harmful, ideologically-driven agenda.

Until reviews like this are shaped and conducted by those they claim to represent, any talk of ‘overdiagnosis’ will continue to sound less like healthy, scientific investigation and more like deep, cynical suspicion.”

DHSC declined to comment on the HSJ article.

*This document was obtained from the National Archives through the efforts of disabled barrister Valerie Eliot Smith, who has ME

**Sir Stephen Timms, minister for social security and disability

9 October 2025

 

 

Coach firm to pay thousands to accessible transport activist after driver lied that he threatened violence

A coach operator that passed on defamatory lies about a well-known disabled activist who exposed the inaccessibility of one of its coaches will have to pay him substantial damages, and make a humiliating apology in open court.

A driver for Bolton-based Tyrers Coaches fabricated claims about Doug Paulley, alleging he had threatened a Network Rail coordinator with violence and that he hurled swearwords at him over an access failure at Rochdale train station 13 months ago.

Tyrers had passed on the allegations to the Driver and Vehicle Standards Agency (DVSA), and another transport company, Arriva.

The incident occurred after Tyrers – which was one of the companies providing a rail replacement service on behalf of government-owned Northern Trains – had been unable to accept Paulley onto its vehicle because the relevant door was not working.

Coaches from two other companies were also not able to accept Paulley on board, with one driver not trained to operate the accessibility equipment, and the other vehicle not wheelchair-accessible.

Tyrers later told DVSA and another transport company, Arriva, that Paulley had threatened violence, was physically threatening, called its driver “a d**khead” and told him he didn’t know what he was “f***ing doing”.

Paulley later discovered by accident – when his solicitor submitted a subject access request to DVSA in connection with another discrimination case – what Tyrers had said about him.

The coach company was unaware that Paulley – who has spent years exposing access failures across the transport industry – had recorded the incident on a camera attached to his wheelchair.

He was able to use the recording to show that none of the claims made by the Tyrers driver had been true.

He decided to launch a defamation claim in the high court because of the risk of serious damage to his reputation, and – he told Disability News Service – because he wanted to address the “reprehensible”, discriminatory and dishonest behaviour of transport companies and coach drivers, and their “horrific, hateful, ableist behaviour”.

Tyrers has now agreed to pay him £7,500 in damages and a further £1,000 for a breach of data protection law.

The company will also have to write to DVSA and Arriva, making it clear that the allegations it shared were false.

And it will have to apologise in open court for the false claims it made, and for the distress and damage caused to Paulley’s reputation.

Tyrers had not commented on its actions by 11am today (Thursday).

Train company Northern has also apologised to Paulley, after one of its managers claimed in an email that he “goes around Railway Stations and tries to find fault at each location”.

The email had been sent out after Paulley complained about the Rochdale incident, in which he had been “simply trying to travel and encountered genuine accessibility barriers” with the rail replacement bus service.

He told Northern in a complaint: “When I documented these experiences, it was as part of my legitimate role as a nationally recognised transport accessibility advocate, not as malicious troublemaking.

The suggestion that I ‘go around’ railway stations looking for problems fundamentally misrepresents evidence-based documentation of accessibility failures as some form of personal vendetta.”

He said the language used showed “a concerning institutional prejudice against disabled passengers who exercise their legal rights to document accessibility failures and hold operators accountable”.

And he said it had “contributed to the toxic atmosphere” that enabled the discriminatory behaviour by Tyrers, and the subsequent “inaccurate, defamatory allegations” that were made about him.

Paulley said Northern’s actions had created “chilling effects that may deter other disabled passengers from reporting legitimate concerns”.

Northern has now apologised in an email for the distress caused by its manager’s comments and told Paulley his campaigning was “invaluable” and “helps us learn from our mistakes” and that his work over the years “has been greatly appreciated and has played an important role in helping us improve”.

Paulley’s data protection case against another transport company is ongoing.

A Northern spokesperson said the company had no further updates to the apology issued to Doug Paulley.

But he added: “As referenced [in the emailed apology], the work that campaigners including Mr Paulley do is invaluable.

The comments in the email about which the complaint was received are not reflective of Northern’s views, and we are truly sorry for any distress caused by these comments.”

9 October 2025

 

 

Access to Work dossier of evidence shows ‘real harm’ and job losses caused by DWP cuts and failings

The Access to Work scheme is failing Deaf and disabled people, and its “decline” in the last two years has caused them “real harm”, with some support packages cut by 80 per cent, according to a detailed dossier of evidence prepared by a user-led organisation.

The 33-page report was put together by London-based Action on Disability (AoD), which said its evidence shows “systemic administrative failure, lack of transparency, and potential breaches of equality and human rights obligations” by the Department for Work and Pensions (DWP). 

The evidence has been sent to the National Audit Office (NAO) as part of its ongoing investigation into how DWP is addressing “challenges” in the operation of the Access to Work (AtW) scheme.

NAO launched its investigation earlier this year following concerns that increased demand for AtW support, and other factors, had “adversely affected DWP’s administration of the scheme”, with “growing backlogs of people waiting for their applications to be processed or their claims to be paid”.

Much of the AoD report is based on its experience assisting disabled people with their AtW applications, renewals and appeals, in which their awards were “reduced, delayed, or rendered unusable due to unimplementable conditions”.

Between January 2023 and July 2025, it says, average support hours per week for more than 35 work placements it monitored have fallen from 22.5 to just four, while the average waiting time for an AtW case manager to be allocated has risen from eight weeks to 30, the job retention rate has halved from 88 per cent to 43 per cent, and the progression to paid work for those on supported internships has fallen from 72 per cent to 28 per cent.

Employers working with AoD say the deterioration of the scheme since 2023 has led to “job losses, reduced hours, and withdrawal from inclusion programmes that were previously successful”, with a significant decline in confidence in AtW among employers.

The dossier was shared with Disability News Service (DNS) this week, just days after DNS reported how disability minister Sir Stephen Timms admitted signing off on a directive that led to widespread cuts to disabled people’s AtW support packages.

Sir Stephen admitted to DNS last week that he had signed off on an order for AtW staff to apply guidance more “scrupulously”, after civil servants submitted a “proposal” to him to approve.

Among its concerns, the AoD report says changes to the way the scheme operates have made it harder for disabled people to contact their AtW case manager, while leading to inconsistency around quotations, inconsistent decision-making, and delayed or unclear pathways for appeals.

The effect of the changes has been to exclude disabled people from employment, destabilise supported internships, and undermine employers’ commitment to inclusion.

This has left AtW no longer operating “as a transparent, accountable, or lawfully administered scheme”, says the report.

The impact of changes over the last two years has been “a significant reduction in awards, increased administrative delays, and a breakdown of communication between AtW and service users, reversing years of progress in inclusive employment”.

And it says its evidence suggests that DWP has refused to publish internal policy instructions; denied claimants procedural fairness; obstructed transparency; and failed to ensure economy, efficiency, and effectiveness in public spending.

The report particularly highlights what AoD calls a “systemic policy shift”, with many applications that would previously have been awarded 100 per cent of a disabled person’s support needs in the workplace now being awarded about 20 per cent of their assessed needs.

This occurs when AtW categorises the assistance requested as a “job aide”, meaning the support worker is viewed as performing part of the job on the claimant’s behalf, rather than helping the disabled employee to overcome barriers related to the work.

AoD says AtW’s “rigid” approach fails to recognise the “legitimate” support that many disabled people need to complete their work independently, such as prompting and structured guidance.

It says AtW’s lack of recognition of such an approach to support has led to significant funding reductions of up to 80 per cent, disproportionately affecting people with learning difficulties, autistic people, those with acquired brain injury, or people with sensory processing impairments.

The report says the 20 per cent award policy “is like handing someone a plank that only stretches a fifth of the way across a river and then blaming them when they fall in”.

The NAO said its report was likely to be published early next year, and its team was still “gathering evidence through different methods”.

A government consultation on the future of Access to Work closed on 30 June, and DWP says it is now reviewing those responses and the scheme and working with disabled people and others on its proposals.

A “collaboration committee” on Access to Work – whose members have remained anonymous – concluded its work this month, and DWP says its views and concerns will now help shape the department’s policymaking.

DWP continues to insist that no changes have been made to AtW policy.

David Buxton, chief executive of AoD, said: “Access to Work should be a bridge into employment.

Instead, thousands are being left stranded mid-way.

The scheme’s decline is costing jobs, damaging wellbeing, and wasting public money.

We hope the NAO’s inquiry restores transparency, fairness, and trust.”

A DWP spokesperson said: “We inherited an Access to Work scheme that is failing both employees and employers, which is why – as part of our welfare reform – we consulted on how it could be improved.

We are reviewing all aspects of the scheme and will develop future policy with disabled people and the organisations that represent them.”

Meanwhile, disability consultant Alice Hastie, who specialises in providing AtW advice, warned this week that DWP had now shut down the AtW complaints email address, which she said “seems like a bizarre (and barely legal!) way of reducing the number of complaints they have to deal with”.

DWP said last night (Wednesday) that its policy is that email is not a valid contact method for complaints unless this has been agreed as a reasonable adjustment.

It is believed that the complaints email may have been shut down because it was for internal use only and its existence was not supposed to have been leaked to claimants.

9 October 2025

 

 

Greens show contrast with other major parties on disability cuts and refusal to stir up hostility to claimants

The Green Party is set to continue to contrast its policy approach on disability with other political parties by supporting disabled people who rely on benefits and have already experienced years of austerity cuts.

The newly-elected leader of the Green Party of England and Wales, Zach Polanski, told members at their annual conference in Bournemouth that the party would fight for the many disabled people “who have found themselves at the sharp end of brutal government cuts”.

His speech was focused on reducing the cost-of-living and addressing “rip-off Britain”, demanding more from “the very wealthiest”, tackling climate breakdown, attacking the “alarm bells of authoritarianism” within the Labour government, supporting the NHS and community cohesion, protecting “rights” and “liberties” through a “politics of hope”, and supporting migrants.

But there was almost no mention of how the party would fulfil these pledges, other than a repeated emphasis on wealth taxes, although its general election manifesto last year pledged a five per cent increase in the level of disability benefits, free personal care for adults, and more money to support disabled children in mainstream schools.

The difference in emphasis from the Liberal Democrat conference – where party leader Ed Davey spoke in an interview of targeting disability benefit fraud – and particularly the Labour, Reform and Conservative party conferences (see separate story), was clear.

There were no attacks on disabled people claiming benefits in Polanksi’s speech, and no calls for cuts to spending on supporting disabled people, or complaints about the “over-diagnosis” of mental distress or neurodivergence.

Instead, he said his party would fight for hard-pressed families, renters who live in “shoddy accommodation” and are wary of further rent increases, and “thousands and thousands of disabled people in the UK who have found themselves at the sharp end of brutal government cuts”.

In his speech, Polanski mentioned meeting a disabled man and his carer while knocking on doors with another Green politician, and how they spoke about “how hard everything is and how it just didn’t feel like a single person was representing them”.

Despite his words, there was still no clear picture of what Polanski and the Green Party would do to change that, other than “focusing day-in, day-out on the cost of living”.

One of the party’s co-deputy leaders, Rachel Millward, had told the conference of her experience of physical impairment and associated “horrendous” pain in her 20s, when she had a blue parking badge and an adapted vehicle.

But she said: “Far worse than that was the pain of separation from my community and from nature.

Conference, please let us always make it a priority to find ways to give people with disabilities much better access to both.”

The contrast with the four main UK-wide parties continued this week, when the Green Party’s other co-deputy leader, Mothin Ali, attacked the “divisiveness and hatred” of the Conservative party and its announcements at its conference in Manchester this week (see separate story).

He said: “The package so far – turbo-charged welfare cuts, draconian anti-migration measures, and axing life-saving foreign aid – would leave few but the wealthiest unscathed.

These measures are a cruel attack on the sick and disabled, migrants and asylum-seekers, and some of the poorest communities in the world.”

9 October 2025

 

 

New film celebrates 10 years since ‘moment in time’ victory over care charges in London borough

A new film released to celebrate 10 years since activists won a campaign to stop their local council charging for care shows how disabled people can achieve important victories by taking collective action, say campaigners who fought for that success.

The film* highlights the eight years of campaigning by Hammersmith and Fulham Coalition against Cuts (HAFCAC), which led eventually to their London borough scrapping home care charges in April 2015.

The campaign began in 2006 when the new Conservative-led council introduced a policy that imposed charges for home care.

HAFCAC was set up to fight the “discriminatory policy”, and it spent eight years lobbying councillors, holding protests and pushing the council to change its policy.

Tara Flood, one of the HAFCAC steering group members, says in the film: “There’s something particularly awful about receiving, through the post or via email, a document, an invoice, that sets out how much you have to pay to enable you to live at home with the support that you need to participate in your community, to be a friend, to be a family member, to be a parent, to get to work.

No-one else is experiencing that.”

HAFCAC also backed a judicial review legal action against the charges brought by three disabled people from the borough who received home care.

Although they lost the case, one of the high court judges described the policy as sacrificing home care services on the altar of council tax reductions.

The film describes how the coalition raised much of its funding with pub quizzes, at which disabled activists such as Flood, Kevin Caulfield and Debbie Domb – all members of HAFCAC’s steering group – began to build relationships with politicians, including Labour’s Steve Cowan.

Cowan, who would go on to lead Hammersmith and Fulham council, says in the film: “The crucial thing was what Debbie, Tara and Kevin were able to do, was educate me and my colleagues on the need for the social model of disability to be right at the heart of our Labour administration’s approach.”

Months after Labour won back control of the council in May 2014, Cowan announced that Hammersmith and Fulham would be scrapping all home care charges in May 2015.

It remains one of only two councils in England that do not charge for home care, after Tower Hamlets council in east London scrapped adult home care charges from April this year.

Caulfield says in the film: “That moment [in 2014] was a real moment in time to show that campaigning does work, that disabled people getting together and collectively taking action can really have an impact.”

David Webb, a fourth member of the HAFCAC steering group, who ran the fund-raising pub quizzes, describes in the film how having personal assistance has completely changed his life.

He says: “It has given me a measure of choice and control that I didn’t have before.”

Victoria Brignall, who has benefited from scrapping care charges in the borough, says in the film: “People don’t choose to be disabled.

It’s a tax on disability and we would like disabled people to be treated in the same way as other people.

You don’t charge people to send their children to school, or to use parks, or to collect your rubbish, so why charge disabled people for their care?”

She says she hopes other councils will now be inspired to abolish home care charges.

Last year, Disability Law Service published research which showed that disabled people across England were continuing to face unlawful discrimination and inequality on an “unparalleled” scale due to “unjust” social care charging policies.

Caulfield points out in the film that tens of thousands of disabled people every year are taken to court for non-payment of care charges.

That’s just a disgrace,” he says.

He and his fellow HAFCAC veterans say the film serves as both a celebration and a rallying cry, and that they hope their success “will inspire more disabled people to take action”.

The film, launched on Tuesday, is dedicated to Debbie Domb, “a fearless freedom fighter for disabled people’s rights”, who died in 2018.

*The film, ‘£12.40 an Hour for a Shower: The Story of Disabled People’s Struggle to Abolish Home Care Charging in Hammersmith & Fulham’, was directed, edited and produced by disabled film-maker, journalist and author Richard Butchins, and can be accessed with BSL and subtitles only, or with added audio description.

**Inclusion London is campaigning to persuade the government to scrap all social care charges.

9 October 2025

 

 

Other disability-related stories covered by mainstream media this week

Thousands of sick or disabled people will be helped into work through a major push to place job advisers in GP surgeries, the DWP has claimed. Work and pensions secretary Pat McFadden is announcing a £167.2 million expansion of the Connect to Work programme to nine further areas across England, including Cumbria, Oxfordshire, and West Sussex and Brighton: https://www.mirror.co.uk/news/politics/dwp-change-affect-gp-surgeries-36033854

Jobcentre work coaches say they are struggling to find employers who can accommodate disabled people and get them into work. The BBC spoke to two work coaches, who said opportunities are hardest to come by for those with long-term health conditions who may require a level of flexibility or additional support. It comes as new data obtained by the BBC from the Department for Work and Pensions suggests that the number of jobseekers finding work each month is falling: https://www.bbc.co.uk/news/articles/c4gz9njvj43o

9 October 2025

 

News provided by John Pring at www.disabilitynewsservice.com

Oct 082025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

4pm to 4.15pm

Tuesday 14th October

Outside the Senedd (Welsh Parliament) in Cardiff

 

The words "We want an Independent PIP Review" in bold and black text, with Independent highlighted in red. On the left there is a tear-out effect of a greyscale photo of a disability protest, and a red-tinted photo of Stephen Timms, the disability minister.

The Disability Minister Stephen Timms was forced to promise UK parliament that there would be no more PIP disability cuts until a review had been co-produced with disabled people.

He has broken this promise.

Disabled people want to run our own, independent, and democratic PIP review.

Disabled People Against Cuts Cymru (DPAC Cymru) will be handing in our open letter with 700 signatures from individuals and organisations. We are calling on the Welsh government to do its part and practically support Disabled People’s Organisations to carry out the review.

Placards, in English and Welsh, with the Disabled People Against Cuts Cymru logo, will say:

“No disability cuts! Disabled people want to run our own independent PIP review. We’re asking the Welsh Government to do its part!”

 

If you are able to, would you consider…

Joining us at the lobby in person on Tuesday 14th.

This will involve: being outside for 15 minutes with placards and possibly a megaphone.

Ask your Senedd member to meet us there.

Let people knowour Google Drive has bilingual social media graphics and placard text, as well as alt text for social media graphics accessibility.

We welcome all support!

 

Access requirements

Is there anything that would help you take part? Is there anything we can do better? Do you have any access requirements? Let us know! Email <dpac.cymru@gmail.com>

A limited number of PPE masks will be available for free.

 

 

Social media graphics

This is a graphic advertising a protest. The top half of the image is a picture of the Welsh Government building (the Senedd) with a blue tint, and the bottom half is a ripped paper effect. Text on the top half, in big letters, says: “Protest (Senedd Disability Lobby)”. On the bottom half, text says: “We will be handing in 30 pages of signatures. No disability cuts! Disabled people want to run our own, independent, PIP review.” In bold, it says “We’re asking the Welsh Government to do its part. Tuesday 14th October 2025.” Next to a red map pin, it says: “Cardiff, outside the Senedd, 4pm to 4:15pm”. To the right is the Disabled People Against Cuts Cymru logo, which is a red, pink, blue, green wheel being held by four hands of different skin tones. At the center of the logo is an upside-down black triangle bearing the letters D P A C and the word Cymru.
A graphic of the DPAC Cymru logo. There is the main DPAC logo to the left, which is a red, pink, blue, and green circle being held by four hands of different skin tones, with the words "disabled people against cuts" surrounding it, and an upside-down black traingle in the middle bearing the letters D P A C. On the right is the word Cymru (pronounced cum ree) (C Y M R U) in large letters, and the background of the letters are cutouts of the Welsh flag. Above Cymru (pronounced cum ree) is written the words Disabled People Against Cuts. Below Cymru (pronounced cum ree) are the words Rights, not charity, and the equivilant phrase translated into the Welsh language.
Oct 022025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Minister admits signing off on order that led to widespread cuts to Access to Work 1

All the evidence from Labour conference points in one direction: More cuts to disability benefits 2

DWP paid nearly £90,000 to disabled claimant left homeless and at risk of harm after years of errors 6

Disability minister struggles to point to any significant achievements in his first year in post 8

Labour ignores disabled people and accessible housing crisis – again – as it announces plans for new towns 10

Labour uses conference to sideline disabled people… unless they are working 11

Labour’s attacks on rights ‘have led to massive resurgence’ in disability movement, protest hears 12

Minister asks DWP to consider releasing secret reports on deaths to grieving relatives 15

No 10 meeting sees Labour hold out olive branch to disabled activists after breakdown of trust over cuts 17

Activist tells conference meeting: Hostile rhetoric under Labour has left me feeling hounded and unsafe 19

Disability Labour priced out of conference after cash-strapped party withdraws financial support 20

Other disability-related stories covered by mainstream media this week 23

 

 

Minister admits signing off on order that led to widespread cuts to Access to Work

The disability minister has admitted signing off on orders that have led to widespread cuts to disabled people’s Access to Work support packages since Labour came to power.

Disabled campaigners have been warning for more than a year of DWP cuts and inconsistent decisions on their Access to Work (AtW) claims, while there have also been mounting concerns about lengthening waiting-lists for decisions on claims.

But when social security and disability minister Sir Stephen Timms was challenged by an MP on the apparent cuts earlier this summer, he insisted that no changes had been made to Access to Work policy, although work was “underway to improve Scheme decision-making by applying the guidance with greater consistency”.

He still insists that ministers have made no changes to AtW policy.

But Sir Stephen has admitted to Disability News Service (DNS) that he signed off on an order for Access to Work (AtW) staff to apply the guidance more “scrupulously”, after being presented with a “proposal” from civil servants which they submitted to him to approve.

The confusion over who was responsible for the move began when DNS asked him who in the Department for Work and Pensions (DWP) had asked AtW civil servants to carry out the demand to be more “scrupulous” in applying the guidance.

He replied: “Well, the department, I guess.”

Asked if it was definitely not him, he said: “I’m not sure… I don’t want to give you a misleading answer.”

But when asked by DNS why he thought AtW staff were suddenly following guidance more scrupulously, he said he had no “no doubt seen a submission, which I have said ‘OK’ to, saying that it’ll be scrupulously applied, to achieve consistency apart from anything”.

He added: “The way things work is a proposal goes into a submission, which comes to me, and I say, ‘OK,’ and it’s very likely that I’ve been advised that we are going to apply the guidance more scrupulously.”

During the interview at Labour’s annual party conference in Liverpool, Sir Stephen said he could not remember when he signed off on the order, but that he would find out.

But when DNS suggested it would then be possible to secure this order through a freedom of information request, he suggested that DWP would resist this request because such an order would have been “advice to ministers” – which would not have to be released under the Freedom of Information Act – even though the instructions would then have been sent out to all relevant AtW staff.

Just minutes earlier, he had claimed that Labour DWP ministers were “very substantially changing the culture of the department in a pro-transparency direction” (see separate story).

Sir Stephen then claimed that the order to AtW staff might not have been written down, and that it might only have been passed on through “a conversation, a staff meeting; who knows how it’s promulgated”.

He later declined several opportunities to welcome the increase in AtW claims, which he called a “huge surge in the number of applications”.

He said the increase meant “people are having to wait longer” to have their claims dealt with, which was “a big part of why we need to reform Access to Work and why we’re consulting on it”.

Asked again if it was a good thing that more disabled people were applying to AtW, he said: “I think there’s a lot to be said for Access to Work and the opportunities it opens up to people.

But we’ve got to have a system that works efficiently and does not keep people waiting for weeks and weeks and weeks.

And that’s the aim of our reform that we consulted on in the [Pathways to Work] green paper.”

The government’s decisions on AtW reform are set to be announced later this year.

2 October 2025

 

 

All the evidence from Labour conference points in one direction: More cuts to disability benefits

Information from Labour ministers and other party sources has shown beyond any doubt that the government is preparing for further attempts to cut spending on disability benefits over the next 12 months.

As disabled people who rely on benefits await the publication of a disability benefits white paper in the next couple of months, it became clear at the party’s annual conference in Liverpool that further cuts are being planned.

Disability News Service (DNS) has this week interviewed the minister for social security and disability; spoken to disabled party members; attended fringe events; spoken (briefly) to a former employment minister; and listened to speeches by the prime minister and the new work and pensions secretary, Pat McFadden.

DNS has also received a Labour briefing; read articles by other journalists with better government connections than DNS; and listened to a broadcast interview with Sir Keir Starmer, in which he said there was a “moral case” for reducing the number of young people with “mental health issues” on benefits.

The weight of this evidence makes it clear that – despite this summer’s government U-turn over billions of pounds of cuts to personal independence payment (PIP) – further cuts to disabled people’s support are on the way.

Two key targets for cuts are likely to be PIP and the health element of universal credit, and almost certainly one focus will be on those receiving support on the grounds of mental distress and trauma, particularly younger people.

On Monday, the chancellor, Rachel Reeves, announced new details of a “youth guarantee” – first announced last year – through which every 18-to-21-year-old in England would be guaranteed either a place in college or university, an apprenticeship, or one-to-one support to find a job.

Any young person still out of work, education or training after 18 months would be given a paid work placement.

The party later confirmed to DNS that there would be “conditionality” – which is likely to mean their benefits would be cut or stopped if the placement was turned down – although there would be “exemptions”, likely to include some sick and disabled young people.

Details on whether those forced onto these placements would receive at least the minimum wage will not be announced until next month’s budget.

McFadden strongly linked “dignity” with work in his speech to the conference, and he said he wanted an “opportunity welfare state” rather than a “dependency welfare state”.

Opportunity, he said, “starts with work”, and he added: “Make work the pathway to dignity, security, and pride.”

McFadden had already alarmed many disabled people before the conference, when he claimed there were “incentives” in the system for people to declare themselves unfit for work so they can “double their money”, and also claimed people were “declaring themselves long-term sick”.

Asked about those earlier comments this week, Sir Stephen Timms, the minister for social security and disability, said he thought McFadden was “onto something here” and had not made a mistake with those comments.

He pointed to the increase in the universal credit basic allowance and the cut in the “health premium” which he said were designed to prevent “quite a serious problem in the current system that is forcing people to aspire to be designated LCWRA* as a kind of destination” so they receive more benefits.

But he did insist that Labour ministers “have the backs of disabled people who can’t work”.

He said: “We are determined to open up opportunities for those who can work, but also to make sure that those who cannot work, and there will always be people who cannot possibly work, and we well understand that, that they will be properly supported.”

He insisted that government ministers had not “dialled up the rhetoric” on disabled claimants, were “making a very good fist of managing a challenging situation”, and that they were not scapegoating disabled people.

He said: “That is not our intention, and I don’t think that’s what we’re doing.

What we are wanting to do is opening up opportunities for disabled people who for too long have been barred from opportunities they ought to be able to take advantage of.”

But Ellen Morrison, one of the most influential disabled activists in the party, as the representative of disabled members on Labour’s national executive committee, told DNS this week that McFadden had been “hinting at the worrying direction that this is going to take”, which looks like “increased conditionality”.

She said: “They are consistently making young people the target. We have to be really careful in the disabled people’s movement not to allow young people to become the target.”

In combination with the existing cuts to the universal credit health element, to be implemented for new claimants from next April, she said the government’s new policies suggest there will be “people who might be forced into either taking inaccessible or unsuitable work, or they are going to be faced with sanctions or destitution.

I don’t think you give people the support that they need by punishing them.”

She said this was combined with the government’s failure to commit to increased funding for the Access to Work disability employment scheme (see separate story).

Morrison said: “I don’t think it’s really about supporting people into work at all.

I don’t believe that’s the motive behind this. It’s to get people off benefits and off any kind of financial support. It’s really short-term thinking.

It’s going to be young people first and there’s more to come for disabled people. A lot more to come.”

The i Paper reported that McFadden was working with Reeves to “craft changes to the welfare system” as a replacement for the cuts the government had to abandon over the summer, and that they would be “laid out step by step over time rather than launched in one big package, in a bid to minimise the risks of a major political backlash once again”.

It also reported that Reeves told a conference fringe event on Tuesday: “A thousand people are going onto PIP claims a day, the majority of those are young people going on to disability benefits with mental health problems.

I’m not denying there are mental health problems; there are massive mental health problems, especially post-Covid.

But I would prefer to be using money to help support people to get into work and to get that treatment in the health service than to pay people to be on benefits and often have them trapped out of work without the support that they need.

I didn’t win that argument, we didn’t win that argument this year, but we can’t go on like this and keep adding to welfare costs.”

The concerns that the government plans to target young people with mental distress were further heightened by the prime minister in an interview yesterday (Wednesday) with BBC Radio Four’s Today programme.

Sir Keir Starmer was asked by the BBC’s Nick Robinson if he was “prepared to say, as prime minister, that being anxious, even being depressed, is a terrible thing to have, but it’s not a good enough reason to stop looking for work”.   

In response, the prime minister made it clear that cuts were coming and he suggested that the government wanted to provide support services for those with mental distress instead of – as highlighted by at least one concerned disabled activist – both benefits and support.

He told Robinson: “I think we need to look again at this issue of mental health and ask ourselves a fundamental question, which is: would we not be better putting our money in the resources and support that is needed for mental health than simply saying it’s to be provided in benefits.

And we’re not saying you shouldn’t have benefits for mental health issues, but I do think we need to examine this quite carefully.”

He said he was “particularly concerned about young people” and the number of young people who are on benefits for mental health reasons.

He said that was “wrong” because “if you are on benefits in your 20s, it is going to be extremely difficult to get off benefits for the rest of your life”, adding: “So there’s a moral case for changing that that I’m perfectly prepared to make.”

The government’s reluctance to reassure those unable to work was demonstrated by a brief exchange between DNS and former employment minister Alison McGovern, now a minister for local government and homelessness, who was speaking in a fringe meeting on the “dignity of work”.

Asked what her message was to those disabled people unable to work because they were not well enough to do so, and about the shortage of jobs that are available and suitable for sick and disabled people, she offered only half-hearted reassurance.

She said: “My message to disabled people is we believe in their right to work, like everybody else.

All the discussions we have been having [are] about trying to make that work suitable and appropriate.

We must always protect people who can’t work, but through new technology and forms of work I think that opens up chances and opportunities for disabled people and others and I want to make sure that people are able to take up those opportunities.”

After the meeting, DNS tried twice to engage with McGovern to ask her to provide further reassurance for sick and disabled people concerned about the government’s policy, but she twice declined to comment further, even briefly, saying she had another engagement to attend.

During the event she had heard from the non-profit organisation Timewise, which has just published research showing that only 2.5 per cent of sick and disabled people who are off work long-term move back into work in any given year.

Of the few that do, more than half (57 per cent) go into jobs that are physically demanding and are associated with higher levels of unpredictable, inflexible and excessive hours.

This contributes to another finding, that more than half of the jobs taken by those who were formerly “inactive or long-term sick” do not last for more than four months.

*Limited capability for work-related activity

2 October 2025

 

 

DWP paid nearly £90,000 to disabled claimant left homeless and at risk of harm after years of errors

A disabled person was left with “ongoing risks” of harm for more than five years – and was even left homeless – after the Department for Work and Pensions (DWP) missed multiple opportunities to provide them with the benefits they were entitled to.

It took the intervention of the Independent Case Examiner to correct the years of errors with their various claims, which led to them receiving a payment of £55,000, as well as compensation of £3,000 for the “hardship” DWP had caused.

They had already received an arrears payment of nearly £30,000 in 2023, after their state pension had been wrongly stopped for four years.

The case was discussed in the annual report from the Independent Case Examiner, Joanna Wallace, who deals with complaints about DWP, and she revealed that years of errors by the department had caused “ongoing risks” to the claimant, who had “very poor physical health and housing problems”.

Her report shows DWP made at least nine significant errors with the case from 2018 – including multiple missed opportunities to rectify its mistakes – when it started the process to move the claimant from disability living allowance to personal independence payment (PIP).

The errors included a missed opportunity to consider if the claimant needed extra support with their PIP claim; failing to act on a letter explaining they had moved home; and failing to follow up a letter that was returned unopened.

DWP also failed to act in 2020, when the claimant asked why they had not been receiving any pension or benefits since the previous year.

Even when the claimant contacted DWP in 2023 to explain that the lack of benefits had caused a significant deterioration in their physical and mental health, which had left them homeless, the department “continued to miss putting things right” and failed to consider any reasonable adjustments for a new attendance allowance claim.

It also failed to review the claimant’s suspended pension payments.

It was only when the claimant contacted DWP again later in 2023 that their state pension was reinstated, and arrears of nearly £30,000 were paid.

But there was no evidence of an apology, and DWP still failed to consider the suspended pension credit claim, while making a further error with a new pension credit claim later that year.

Eventually, ICE was notified of the case, and it “took the exceptional step of reaching out to DWP immediately so we could work together urgently to put things right for our customer”.

This led to DWP making a payment of nearly £55,000 in connection with the claimant’s DLA, state pension and pension credit claims.

Wallace also recommended a “consolatory payment” of a further £3,000 because of “the errors and lack of vital support to an extremely vulnerable customer, which had clearly exacerbated the long-term issues with their health and their housing situation” while DWP had “continued to miss opportunities to put things right”.

Asked this week if the case showed there were still multiple problems with the benefits system, and how one claimant could have faced so many errors, DWP said it had introduced thorough procedures to investigate and learn lessons from cases where mistakes were made.

It also said that it used sources such as internal process reviews (see separate story) and its Serious Case Panel to identify and address systemic issues, as well as ICE’s reports.

A DWP spokesperson said: “We regret the mistakes that were made in this case and we are determined to learn from them.

We support millions of people every year and our top priority is they get the benefits to which they are entitled as soon as possible, and to ensure they receive a supportive and compassionate service.”

The report says ICE cleared 2,232 complaints in 2024-25, of which 1,514 were investigated, 567 were resolved (an agreement reached before evidence in the case is requested), 97 were settled (an agreement reached after evidence is submitted but before any investigation is carried out), and 54 were withdrawn.

Of the 1,514 that were investigated, 892 (59 per cent) were fully or partially upheld, 618 (41 per cent) were not upheld and in four cases (less than one per cent) ICE was unable to reach a finding.

Of 205 cases relating to disability benefits that were dealt with in 2024-25, 73 were resolved or settled to the complainant’s satisfaction, 121 ICE investigation reports were issued, and 11 were withdrawn.

Of the 121 investigation reports, 53 (44 per cent) were upheld or partially upheld, 66 (55 per cent) were not upheld and in two cases ICE was unable to reach a finding.

*The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP, is published by Pluto Press

2 October 2025

 

 

Disability minister struggles to point to any significant achievements in his first year in post

The minister for social security and disability has struggled to point to any significant achievements on disability equality after more than a year in post, but he insisted that the government does not need a separate minister for disabled people.

The Labour government has been consistently criticised for not appointing a stand-alone minister for disabled people and instead combining that role with the social security brief under Sir Stephen Timms.

But in an interview with Disability News Service (DNS) at this week’s annual Labour conference in Liverpool, Sir Stephen struggled to point to any significant achievements in the 14 months since his appointment, excluding employment and work and pensions issues.

Asked for three key achievements, he pointed first to the publication in July of new five-year plans to improve the use of British Sign Language (BSL) by government departments.

This followed the British Sign Language Act, a private members’ bill introduced under the last Conservative government, which legislated for the government to report on how departments use BSL in their communications.

He also pointed to the government signing the Solfagnano Treaty (PDF) – a watered-down version of the UN disability convention – during a G7 ministerial meeting in Italy last October.

The treaty appears to have been mentioned just once in parliament – last December – since it was signed, and has been almost completely ignored by politicians, the media, and disabled people.

Sir Stephen also highlighted the “preparations” the government was making for a “cross-government plan” on disability.

Asked why there did not appear to have been any discussions with disabled people’s organisations about this plan, he said: “Internally, there’s been lots of discussion, and the fruits of that will become apparent in the coming months.”

Asked about the lack of progress in his role as disability minister, he said: “I think a lot’s been done, actually.

And I’m hoping that the fruit of that will become increasingly apparent as time goes on.”

He said he did not believe his job – with responsibility for both social security and disability – was too extensive, and he said predecessors under Conservative governments also had responsibilities that were “actually quite wide” and extended outside the “strict disability group”.

But disabled activists at the conference – and outside it – repeated the long-standing calls for a separate minister for disabled people.

Emily Pomroy-Smith, a member of Disability Labour’s executive committee, told DNS that disabled people had been calling repeatedly for a separate minister to cover disability, which was a “very, very important” demand.

She said: “The brief is massive, and it is too big for one person to do on their own.

We would [also] prefer it wasn’t sat under the Department for Work and Pensions.”

Disabled activist Klint Durham, who took part in a Disabled People Against Cuts protest outside the conference on Monday (see separate story), said he would also like to see a stand-alone minister for disabled people.

He said the remit of that post would need to cover areas across government, including housing, transport, employment and community engagement.

2 October 2025

 

 

Labour ignores disabled people and accessible housing crisis – again – as it announces plans for new towns

Labour has again ignored disabled people when making a major housing announcement, after revealing plans for a “new generation of new towns” but refusing to explain how it will ensure they are designed to be accessible to disabled people.

Housing secretary Steve Reed told his party’s annual conference in Liverpool on Sunday that the 12 new towns across England would include GP surgeries, libraries, schools, green spaces and transport links.

Building work on three of the new towns will begin before the next general election, with the government working with “world class architects”.

Reed said he would do “whatever it takes” to build the homes.

But Labour this week failed to make any pledge that accessibility would be central to the design of the new towns.

Asked for Reed’s promise to disabled people on the new towns, the Labour party had refused to comment by noon today (Thursday), three days after Disability News Service (DNS) asked the question.

Nearly 15 months after the general election, disabled people are still waiting for the new government to say whether it will introduce stricter minimum accessibility standards for new-build homes in England, three years after a pledge by the last Conservative government – which was never fulfilled – to take action to address the critical shortage of accessible housing.

At last year’s conference, after DNS questioned the party on the failure of ministers to mention the accessible housing crisis, a Labour spokesperson had promised that the government would “set out its policies on accessible new build housing shortly”.

A year on, and disabled people are still waiting for that promise to be fulfilled.

Reed was also the latest Labour minister to say the government was fighting for “hard working people”, apparently ignoring those who are unable to work, including many disabled people who need accessible homes.

He was speaking as an independent report – commissioned by the government – recommended 12 potential locations for new towns across England, with at least 10,000 new homes in each location.

But a brief search through the 135-page report appears to show no mentions of disabled people or the accessible housing crisis, although there is a brief reference to the need for “homes for older people, as well as specialist housing built to accessible and adaptable standards”.

Emily Pomroy-Smith, a member of Disability Labour’s executive committee, said the new towns appeared to be a “really exciting opportunity to set the benchmark for accessibility” and it was crucial for disabled people to be involved in those plans from the beginning.

She said there was no reason why accessibility could not be built into the foundations of the programme.

Disabled activist Flick Williams, a retired disability equality trainer and access consultant, who was in Liverpool to take part in a Disabled People Against Cuts protest outside the conference (see separate story), said she was not at all optimistic about the new towns announcement.

She said the “signs were there” when there was no mention of the accessible housing crisis in last autumn’s National Planning Policy Framework.

She said: “We are just missing from everything they do.”

She said her message to Reed was: “If you want disabled people to be active in the labour market, you need to build us accessible homes.”

2 October 2025

 

 

Labour uses conference to sideline disabled people… unless they are working

The Labour party has used its annual conference to stress – once again – that its focus is on supporting “working people”, rather than disabled people who are unable to work.

In his 6,300-word speech to the conference on Tuesday, the prime minister did not mention disabled people once, other than in relation to the work of carers, care workers and volunteers, and a brief mention of his late disabled brother who he said was “badly failed by the education system”.

In contrast, he mentioned “working people” 17 times, including telling the conference audience that the state will be “accountable to working people”, that he wanted to see “working people in control of their public services”, and arguing that it was “working people who paid the price of Tory decline”, while stressing that “Labour is the party for working people” and that he would “fight for working people”.

The concerns about Sir Keir Starmer’s focus on “working people” date back to 2022 and a speech he made to Scottish Labour’s annual conference, at which he declared publicly that Labour was “the party of working people”.

His chancellor, Rachel Reeves, has an even longer troubling track record, having said 10 years ago that Labour did not want to be seen as “the party to represent those who are out of work” and that it was “not the party of people on benefits”.

In his own speech, earlier on Tuesday, health and social care secretary Wes Streeting stressed his determination to build a National Care Service “worthy of the name”.

Labour’s only significant social care announcement was the first ever fair pay agreement for care workers, with an initial £500 million in funding to deliver “better pay, terms and conditions” for adult care workers across England.

In contrast to the prime minister’s speech, Streeting mentioned disabled people three times, highlighting how many disabled people were now surviving with conditions “that would have cut their lives short thanks to breakthroughs in medical science that allows them to not only survive, but to thrive”.

He said that “if we want to match longer lives with better lives, then we must build a social care system to meet their needs”.

And he highlighted the government’s decision to provide more funding for disabled facilities grants, which has provided “safety, dignity, independence and quality of life”, as well as “the biggest uplift in carers’ allowance since the 1970s”.

It has been clear since at least 2022 that Labour’s priority in government would be lifting the pay of care workers before any moves to reduce or scrap care charges.

Any firm decisions on long-term reform will wait for the conclusions of an independent commission, led by former civil servant Baroness [Louise] Casey.

The first phase of the commission will report next year, but the second phase, with recommendations for longer-term reform, will not be completed until 2028.

Last year, Disability Law Service published research which found that disabled people across England were continuing to face unlawful discrimination and inequality on an “unparalleled” scale because of “unjust” social care charging policies.

2 October 2025

 

 

Labour’s attacks on rights ‘have led to massive resurgence’ in disability movement, protest hears

The Labour government’s attack on disabled people’s support has led to a “massive resurgence” in the disabled people’s movement in the last year, a protest outside the party’s annual conference has heard.

Monday’s protest highlighted Labour’s failure to stop the “slow violence” that has led to the killing of countless disabled benefit claimants at the hands of the Department for Work and Pensions (DWP), and the government’s refusal to act on the genocide in Gaza.

The Genocide Abroad, Democide at Home protest was held just outside the boundary fence of Labour’s annual conference in Liverpool.

The speeches were at one point being watched by nearly 100 protesters and passers-by.

The aim of the protest was to draw parallels and links between the genocide in Gaza and the “democide at home”, with activists believing that thousands of disabled people have been killed by Department for Work and Pensions (DWP) state violence in the last 15 years.

But it also expressed solidarity with trans rights activists and called for links between the three movements.

The protest began with a recording of the names of more than 100 disabled people who had lost their lives through DWP’s actions and failings, including Errol Graham, Jodey Whiting,  Stephen Carré, Roy Curtis and Faiza Ahmed and more recent victims of DWP bureaucratic violence such as Tracie, Kevin Gale, and David.

The protest was organised by Disabled People Against Cuts (DPAC) branches from Merseyside, Leeds, Manchester and York.

Rick Burgess, from Manchester DPAC, said the Labour government had not tried to reverse the Conservative cuts to disability support but instead “attempted to push farther and further”.

He said the attempted cuts to personal independence payment would have led “to many more deaths”, but disabled people forced the government to back down.

He said: “We did that. We started the end of this absolutely pathetic and failed Starmer government.”

He then led a chant of “no more benefit deaths”.

Burgess added later: “We still have a political system that absolutely denies disabled people’s right to live a good life on equal terms with everyone else.

We need social security, we need social care, and we need social justice.”

Referring to Gaza, he said: “If governments see genocide is a viable policy solution, they will start thinking about using it elsewhere.”

Billie Gibson, from Crips Against Cuts Merseyside, led a series of chants, including “Keir Starmer, disabled harmer” and “don’t cut PIP, tax the rich”, before telling the protest that the “warfare on disabled people needs to stop”.

Dr China Mills, who leads the Deaths by Welfare project at Healing Justice Ldn, told protesters: “Disabled people have been telling us for well over a decade that the welfare system is killing people, and Labour, from New Labour to now, have cooked up many of the policies that kill people.

People are being killed because the government doesn’t think that disabled people matter or have any value and because to them work equals worth.

We think that these killings go deeper than mistakes or flaws in the system.

The system isn’t broken; it is functioning exactly as it was designed.”

Jessica Ryan, from Disability Rebellion, which helped promote the protest online for those who could not attend in person, highlighted the impact of Labour’s cuts on the next generation of disabled people, and the unfairness of the government’s treatment of disabled people.

Rhi, from Merseyside DPAC, but also a researcher for the Trans Safety Network, said: “This is a government that seems extremely determined to be remembered for its genocidal foreign policy and its democidal domestic policy, as well as attacking our right to protest.

As a disabled and trans person, I have long insisted that disabled people’s liberation and trans people’s liberation will be one and the same fight, and that our oppression is built with the same tools, but these last few years have made this increasingly clear to more and more of us.

It is a terrifying time to be a disabled person in the UK right now and it is a terrifying time to be a trans person here, too.

Disabled people and trans people are under attack but when we join together to fight back, we are much, much stronger.”

Emma Hewitt, from Leeds DPAC, said she had been a disability rights activist for 20 years but it had only been in the last 18 months that she had “really seen the attacks on us”.

She said: “It’s not just the fact that they are cutting our services, it’s the fact that they are attacking us, they are attacking our right to live.

It’s so painful that not only do they not care about us, but they are quite happy to spend the money that we need for our support on genocide (in Gaza).

There has been a massive resurgence in the disabled people’s movement, and it just fills me with so much hope.

Every town in this country, every city, has got a disability rights group, not just Disabled People Against Cuts, we’ve got Crips Against Cuts, who are this amazing new group, Disability Rebellion, you guys are my heroes, you’ve been finding new ways for us to be able to campaign so no-one gets left behind, so everyone has a voice.”

Disabled activist Flick Williams, from York DPAC, said it was “so important” to be at the protest because the imminent DWP white paper – which is expected to include a series of further cuts to benefits – will be published later this year.

She said she had been struck by the names of those who had been killed due to DWP “slow violence”.

She said: “I just thought: there are going to be so many more.”

Another disabled activist, Klint Durham, told DNS he had travelled to Liverpool from Leeds to show his “contempt for the Labour government and its attack on disabled people and the welfare cuts”.

After 14 years of Conservative austerity, he said, he could not believe that a Labour government “would think to introduce more cuts”, and that it was “very clear” that the Labour-run DWP needed to “listen to organisations of disabled people and not charities”.

*The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP, is published by Pluto Press

2 October 2025

 

 

Minister asks DWP to consider releasing secret reports on deaths to grieving relatives

A minister has asked the Department for Work and Pensions (DWP) whether it could release secret reports to families whose relatives’ deaths have been linked to DWP’s actions and failings.

Ever since Disability News Service (DNS) first revealed the existence of the secret reviews in October 2014, DWP has repeatedly refused to even alert the families of those who have died that an investigation has been carried out.

The department has insisted – as it did last week when it again refused to tell lawyers for the family of Jodey Whiting whether it carried out a probe into her case – that such reviews are “internal retrospective investigations focused on organisational learning, not public accountability”.

The probes were previously known as peer reviews but are now called internal process reviews (IPRs).

The only IPRs ever to be released to grieving relatives have come after orders made by a coroner or a judge.

DNS is aware of only two such cases, including the IPR ordered to be released by the coroner who heard the 2021 inquest into the death of Philippa Day.

But DNS told the social security and disability minister Sir Stephen Timms this week that safeguarding adults reviews and domestic homicide reviews are released to families and are published, although the identities of the subjects of the reviews are disguised.

DNS also pointed to the eight-year campaign for justice and accountability led by Jodey Whiting’s mother, Joy Dove, and her struggle to secure the IPR she believes was carried out into the circumstances surrounding her daughter’s death.

Speaking during an interview with DNS at Labour’s annual conference in Liverpool, Sir Stephen said: “Internal process reviews are what the name implies, they are for internal consumption within the DWP to look at where we got things wrong and how are we going to put them right.

So that is kind of the nature of them, so I don’t think it’s surprising inherently that they are not shared more widely.”

But he then said that DNS was “raising a very reasonable issue here, and particularly asking whether families should, in certain circumstances, be able to see them”.

He said he had asked DWP civil servants “to take a look at this, and I am going to be receiving some advice on that subject”, although he said it was “difficult and there is a duty of confidentiality that the department owes to people”, even after they have died.

He added: “There might be a need to change the law here.

Anyway, I’ve asked officials to have a look at this and to come back to me.”

His comments came after Steve Darling, the Liberal Democrat work and pensions spokesperson, told DNS last week that he was hoping to use the government’s new Hillsborough Law to force DWP to release IPRs to relatives.

During Sunday’s interview, Sir Stephen admitted that it was only because of a DNS news story that he became aware that a report – commissioned by Conservative work and pensions secretary Therese Coffey in 2020 – had called for DWP to reduce suicides of benefit claimants and other “very bad cases”.

The Complaints, Suicides and Other Matters report was written by Tory peer Baroness [Lucy] Neville-Rolfe, but DWP has told DNS that it would be too expensive to find out what happened in response to the 11 recommendations she made five years ago.

Among her recommendations was for DWP to set up a new register of “very bad cases”; to review its safeguarding system, including an analysis of its effectiveness in reducing suicides; and to review the IPR system.

Sir Stephen said on Sunday: “I actually did not know that Baroness Neville-Rolfe had done a report for the DWP until my office told me that you were likely to ask me about it.

That’s the first time I was aware of this report having been done.”

DNS has been writing news stories about the report since May this year, but it appears that no-one in DWP briefed him on the report or those stories until the lead-up to the conference.

Sir Stephen said he would now ask civil servants what happened in response to the 11 recommendations made in the report.

He said: “I will find out about it.”

He said Labour ministers were now “very substantially changing the culture of the department in a pro-transparency direction.

I’m not claiming that we’ve entirely got there yet, but we’ve made a lot of headway.”

Sir Stephen also confirmed that the disabled members of his new independent disability advisory panel would no longer be expected to sign non-disclosure agreements, following a backlash over the “completely unacceptable” measure.

Instead of an NDA, DWP said it would “collaboratively agree the confidentiality arrangements as part of the terms of engagement with the panel once the membership is confirmed”.

The deadline for applications has now been extended by two weeks to 13 October.

*The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP, is published by Pluto Press

2 October 2025

 

 

No 10 meeting sees Labour hold out olive branch to disabled activists after breakdown of trust over cuts

Senior figures in the Labour party pledged to try to rebuild trust with disabled people at a meeting with activists earlier this month at 10 Downing Street, Disability News Service can reveal.

The 90-minute meeting between a delegation of seven disabled people and senior figures within the Labour administration took place on 2 September.

It came after a text message from Joe Watkinson, deputy vice chair of Disability Labour, to Claire Reynolds, who was at the time the party’s political director in Downing Street, but is now Labour’s executive director of stakeholder relations.

Watkinson had suggested the need for a meeting to try to rebuild Labour’s relationship with disabled people after the damage caused by the government’s attempts – later abandoned – to cut billions in spending from personal independence payment, and the cuts that will be introduced through its Universal Credit Act, and to ensure disabled people “have a voice and can be heard in a constructive way”.

He told Disability News Service (DNS) at this week’s Labour conference in Liverpool: “Disabled people cannot afford a Reform government.

The only hope we have is via a Labour government. We need to reset the relationship with disabled members and that’s at the core of everything we need to do.”

Among the disabled people who attended the meeting were representatives of the Co-operative Party – where Watkinson is chair of the party’s disability network – union activists and representatives of Disability Labour (DL), including Kathy Bole, DL’s chair, and Emily Pomroy-Smith, another member of DL’s executive committee.

As well as Reynolds, other Labour representatives at the meeting included a work and welfare special adviser, and a representative of the party’s general secretary.

It is not yet clear what promises the party will make to those who attended the meeting, other than a pledge to hold further such meetings.

But Watkinson said: “It was a very constructive meeting. It was taken seriously. It was a very frank and honest discussion.

For the majority of the meeting, they sat there and listened.”

Pomroy-Smith said: “It was about using our lived experience to inform what they were doing. They were ready and listening.

Claire really did fight for this. She really fought for the meeting to happen, and she’s continuing that in her new role.”

She said the government representatives they met were aware of the level of anger among disabled people at the way the PIP and universal credit cuts had been handled earlier this year.

She said: “What we were coming with was solutions. The focus was how can we rebuild and what does that look like.

It was about moving forward. How do we prevent it from happening again.”

Among the issues raised were the kind of language used by ministers, and inaccurate briefings on social security reform.

Pomroy-Smith added: “At the moment there is a real need to amplify the voices of disabled people and not be spoken about.”

2 October 2025

 

 

Activist tells conference meeting: Hostile rhetoric under Labour has left me feeling hounded and unsafe

One of the only disabled activists to speak at Labour’s annual conference has delivered a powerful rebuke to ministers who have failed to do anything to curb the rising levels of disability-related hostility.

Fingers, a disabled RAF veteran who campaigns with Crips Against Cuts and the new group Disabled Resistance, told a fringe event on Monday how her car had been attacked and she had been called a “scrounger” after a young man saw her blue parking badge on the dashboard.

She told an Amnesty International UK fringe event on fixing the broken social security system: “What the language of the last 18 months has done to me is, for the first time in my life… I feel hounded, I feel unsafe.”

She said she felt as though the hostile rhetoric directed at disabled people had turned her into “a non-person”.

She said: “You’re looking at someone who is unsustainable. Why do I have to be a unit of productivity in this country?

The words we use are fundamentally important. Not one newspaper has run an editorial or article about how these words are making us feel.

I fought for the country, I worked for the NHS, and now I am effectively a ‘useless eater’.”

Fingers, who also used to chair a mental health charity, told Disability News Service (DNS) after the meeting that four young men had walked past her car as she was waiting at traffic lights in Loughborough about a month ago.

They had seen her blue badge and one of them then bounced on the bonnet of her car and shouted: “Bloody scrounger!”.

She wound down the window and gave them a “stream of obscenities and invective”, but later her anger turned to fear for her safety and that of other disabled people.

She told DNS: “The rhetoric surrounding people who require support because of ill-health has become positively threatening.

It has been encouraged tacitly by the government.

It dehumanises people who can’t work and there has been not one shred of fightback by the government about the knock-on effects of their rhetoric.

It has given a licence for anybody at all to pick on and say hateful things about disabled people, and it’s everywhere, and that makes me feel unsafe.”

The former Labour member, who joined the party to vote for Jeremy Corbyn as party leader and left when he was replaced by Sir Keir Starmer, said she had expected this kind of rhetoric from a Conservative government, but it was “shocking” that it had continued under a Labour government, which had even made the situation worse.

She was also critical that the fringe event had been held on an inaccessible stage without a ramp, as highlighted by Daily Mirror columnist Susie Boniface, who chaired an event in the same location within ACC Liverpool.

Although she is not a wheelchair-user, Fingers has a physical impairment and struggled with the inaccessible stage, which she said was “shameful for Labour”.

Because of the lack of chairs in the conference centre, she had already been forced to resort to sitting in the accessible toilet to prepare for her presentation at the fringe event.

She said: “I was in quite a bit of pain when I left that conference. It would have been alleviated if I had had anything other than a disabled loo to sit on.”

DNS reports elsewhere this week that Disability Labour – which often provides free access advice to the party at its annual conference – was priced out of attending this year’s event by the party.

Meanwhile, disabled Labour MP Nadia Whittome told the Amnesty fringe event that she was “really proud” to have played a small part in the backbench rebellion that led to the government withdrawing its planned cuts of billions of pounds to spending on personal independence payment.

But she pointed out that cuts to the health element of universal credit for most new claimants are still going ahead next spring.

She said campaigners must continue to fight against further government cuts to disability benefits, and against disability discrimination, and for investment in public services.

She echoed Fingers’ comments on the political rhetoric and told the fringe event: “People’s worth is not determined by their economic contribution.”

2 October 2025

 

 

Disability Labour priced out of conference after cash-strapped party withdraws financial support

The campaigning organisation that represents disabled people within Labour had to cancel plans to attend this week’s conference in Liverpool after the party asked it to pay thousands of pounds in fees.

Members of Disability Labour appealed for last-minute financial help during a visit to 10 Downing Street earlier this month (see separate story) but were told the party could no longer afford to help it cover its costs at conference.

For the first time since 2018, Disability Labour – which has spent years providing free advice to the party on access issues – was asked to pay for a space for a stand at Labour’s annual conference, but it was told this would cost £2,500.

Disability News Service (DNS) has been told that other Labour-affiliated socialist societies have also had to pull out of attending the conference this week because they could no longer afford the increasing cost and because of the lack of financial support from the party.

The party has told DNS that the changes to financial arrangements at the conference were applied equally to all 21 socialist societies and were not unique to Disability Labour.

Disability Labour said this week that it did not believe it had been singled out.

Last year, it had to pay only a few hundred pounds to cover the cost of electricity and other costs, including hiring a small stand where its members could provide advice to other disabled party members and use as a base to lobby politicians and delegates on disability issues.

It would likely have had to pay thousands more to hire a venue at the conference for a fringe event, and hundreds of pounds more for accommodation in Liverpool.

Emily Pomroy-Smith, a member of Disability Labour’s executive committee, said the party “did express regret” that it had not been able to offer the same support as in recent years, and Disability Labour was now in discussions with the party about future support.

She said: “We want to work with the party to get us back here.

We are asking the party to meet us halfway and work with us so next year we can be back. It’s really important.

In a year where we have seen difficulties and damaged relationships with disabled people and communities, it’s really important that we see a willingness to rebuild that, which we have had.

Obviously, it’s disappointing that we are not able to be here in our normal capacity.

The Disability Labour stand is a hub for disabled people. We end up supporting disabled members and visitors’ access issues and signposting them [to support].

We do provide a service.”

She added: “Conference is getting more and more expensive. That’s not just for Disability Labour.”

Local hotels have increased prices by as much as six times their usual rates, she said.

Joe Watkinson, deputy vice chair of Disability Labour, said: “Disabled members need us to be here. It’s important that we are here.”

Pomroy-Smith and Watkinson were only able to attend because the independent transport trade union TSSA covered many of their expenses, paying for Pomroy-Smith’s accommodation and travel, and travel for Watkinson.

Kathy Bole, Disability Labour’s chair, said they were told at the No 10 meeting in early September that the party’s financial problems meant it could not support Disability Labour at this year’s conference.

Bole said Disability Labour executives had reluctantly decided not to use a large chunk of the society’s limited funds to hire a stand and host a fringe event.

Disability Labour is a socialist society affiliated to the Labour party, but has members from across the Labour spectrum, although its leadership and membership have traditionally supported causes on the left of the party.

It has a long history of acting as a “critical friend” of the party at its annual conference, raising concerns about access, policy and the need for co-production.

It has also spent years lobbying Labour to do more to address disability discrimination within the party.

Last year, it was critical of the new Labour government’s decision to appoint only a part-time disability minister, and supported a disabled delegate who was refused entry to the conference with her assistance dog.

In September 2022, its members supported calls for the party to do more on eliminating the barriers faced by its own disabled members.

It raised similar concerns the previous year, prompting a pledge from the party’s general secretary that he would put an end to the years of discrimination experienced by disabled party members.

And, as part of the party’s online conference in September 2020 – in the early months of the pandemic – Disability Labour pushed the party for a stronger commitment to plans drawn up by disabled people that would solve the social care crisis by setting up a co-produced National Independent Living Service.

Disability Labour has also hosted important fringe events, and in September 2023 its event was attended by four shadow ministers.

This event drew the promise from shadow disability minister Vicky Foxcroft that, if Labour won power, “every single one of our ministers will be ministers for disabled people”.

A Labour party spokesperson said in a statement this week: “We are committed to providing a safe and accessible environment at conference for disabled people.

There are more accessibility stewards working at conference this year compared to last year, and we have also provided these stewards with an increased level of training.

We also continuously engage with Disability Labour on a wide range of issues, including greater celebration of Disability History Month which the party has begun work on.”

2 October 2025

 

 

Other disability-related stories covered by mainstream media this week

The family of a disabled man who died after not being given any food for nine days while being treated in an NHS hospital has told ITV News, “we thought he was having nutrition… but as it turns out, they were starving him.” This comes as an ITV News investigation has revealed a crisis in the care of people with learning difficulties and autistic people. Bereaved families have told ITV News they believe their children died due to failures in NHS care: https://www.itv.com/news/2025-10-01/i-dont-want-to-die-downs-syndrome-man-starved-to-death-in-hospital

2 October 2025

 

News provided by John Pring at www.disabilitynewsservice.com

Sep 252025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Davey stirs up hostility towards disabled claimants, as Lib Dem spokesperson links similar attacks to far right 1

Lib Dems want to use new Hillsborough Law to force DWP to release secret reports into deaths 3

Darling accuses DWP of ‘absolutely shameful’ cover-up over Access to Work changes 4

Disabled activists working with peers to address serious flaws in ‘dangerous’ assisted dying bill 5

UN calls for human rights assessment of government’s benefit cuts bill and mental health reforms 8

DWP is ‘dysfunctional’ and needs major review, says Lib Dem Steve Darling 11

Lib Dems insist they are still focused on social care, despite leader concentrating again on carers 13

New publications ask how disabled people and allies can hold the state to account for welfare state killings 15

Mother left ‘disgusted’ by DWP’s silence over secret report into Jodey Whiting’s death 17

Anger and frustration after DWP’s latest jobcentre announcement and McFadden’s ‘incentives’ comment 19

Other disability-related stories covered by mainstream media this week 21

 

 

Davey stirs up hostility towards disabled claimants, as Lib Dem spokesperson links similar attacks to far right

Liberal Democrat leader Sir Ed Davey has whipped up hostility towards disabled people by suggesting there is widespread fraud among claimants of personal independence payment (PIP), despite his own work and pensions spokesperson linking similar unfounded attacks to the far right.

In an interview with Times Radio at the Liberal Democrat party conference in Bournemouth, Sir Ed suggested the reduction in face-to-face assessments had led to “quite a lot of fraud” among the recent increase in PIP claimants since the start of the pandemic.

But the latest figures from the Department for Work and Pensions (DWP) estimate that just 0.4 per cent of PIP spending in 2024-25 was due to fraud, while the previous year’s estimate had been zero per cent.

Despite these facts, Sir Ed said: “There’s a real suggestion in those numbers, by the way the Conservatives managed the system, that there’s quite a lot of fraud there and surely everyone can agree we should go after the fraud to make sure that people who need the benefits that people who are really disabled can still get them.”

But Sir Ed’s comments came on the same morning (Sunday) that his own work and pensions spokesperson, disabled MP Steve Darling, told Disability News Service that far-right activists were launching similar attacks on disabled claimants using dubious figures on economic inactivity.

Darling said: “My real fear is that in our now Trumpian world, [the far right] don’t need the facts to add up to make outlandish claims.”

He said it was disturbing how “the far right will just make up narratives for their own purposes, and demonising others is part of their playbook and sadly people with disabilities and quite often people with hidden disabilities are in their crosshairs.

It’s part of that push back against the far right [and what] we need to be doing is unpicking that, because otherwise that half-truth will be built on by the far right to demonise people with disabilities.”

Sir Ed also mirrored claims by right-wing politicians when he claimed in the Times Radio interview that it was vital to reduce spending on social security, despite widely-available official figures showing that expenditure is stable as a proportion of GDP*.

His comments on PIP were particularly embarrassing because he focused in his main conference speech on Tuesday on attacking Reform UK and its leader, Nigel Farage, warning repeatedly of the “Trump-inspired country Farage wants us to become”.

Asked about his leader’s comments, Darling declined to say if he agreed with them, but yesterday (Wednesday) he issued a statement through his party’s press office.

He said: “Liberal Democrats are proud champions for the most vulnerable in society.

We led the charge against the government’s ill-thought welfare cuts bill and played an instrumental role in defeating plans to slash PIP.

We will always stand up for disabled people and their carers.

Ed rightly pointed out that the Conservative party’s move to telephone assessments has damagingly undermined public trust in the welfare system.

A fair system of in-person assessments, where possible, is vital to make sure this crucial support is there for people who need it.

More broadly, Liberal Democrats have long argued the best way to reduce welfare spending is to tackle the root causes of the rising welfare bill – by seriously investing in health and care, and making it easier for disabled people to access the world of work.”

Sir Ed’s speech to the conference included just two mentions of disabled people, but neither in relation to his own party’s policies.

Instead, he mentioned family carers like himself 10 times in Tuesday’s speech, without once mentioning the adult social care charging crisis, which sees tens of thousands of disabled people falling into debt every year because of those charges (see separate story).

*Gross domestic product, the size of the country’s economy in a particular year

25 September 2025

 

 

Lib Dems want to use new Hillsborough Law to force DWP to release secret reports into deaths

The Liberal Democrats are set to try to use the government’s new Hillsborough Law to force the Department for Work and Pensions (DWP) to release secret reports into the deaths of disabled benefit claimants.

For years, the department has refused to hand bereaved relatives the internal process reviews (IPRs) it carries out into deaths that have been linked to its actions and failures.

It releases reviews only when ordered to do so by a coroner, or a court, or very rarely on other occasions – there is no record of it doing so in such circumstances – because it insists they are intended for learning purposes within the department.

This week, Disability News Service (DNS) has reported DWP’s latest refusal to release an IPR – or even to say if such a review was carried out – to a family, this time following the death of Jodey Whiting (see separate story).

Her mother, Joy Dove, is in her ninth year of campaigning for justice for her daughter, who took her own life in February 2017.

In a letter to Dove, DWP said IPRs were “internal retrospective investigations focused on organisational learning” and “often contain sensitive personal information about claimants” and so “could be considered a breach of privacy”, even though the claimant is dead.

The letter, from the Government Legal Department, said DWP was “working towards a more open approach to sharing findings and learning from IPRs”, but this is believed to refer only to anonymised recommendations made by the reviews rather than the facts they uncover.

DNS reported in June that a DWP director who gave evidence at the second inquest into Jodey Whiting’s suicide claimed she didn’t know whether an IPR had been carried out and would have to ask colleagues.

The minister for social security and disability, Sir Stephen Timms, came into his post last year pledging to increase transparency within the department.

But he has so far refused to change the department’s position, even though adult safeguarding reviews – sometimes examining the same deaths as IPRs – are released to relatives, and are published anonymously.

Now Steve Darling, the Liberal Democrat work and pensions spokesperson, has pledged to use the government’s new public office (accountability) bill, otherwise known as the Hillsborough Law, to force DWP to publish IPRs and release them to families.

This is because the new bill includes a legal duty on public authorities and public officials “to act with candour, transparency and frankness”.

In an interview with DNS at his party’s annual conference in Bournemouth, Darling said he wanted the bill to produce a “culture change” within DWP and the whole of Whitehall, and that he intends to ask parliamentary questions about how the release of IPRs should be part of that.

He said it should be the same approach as in the aviation industry when there are near misses and “things have gone wrong”.

Otherwise, he said, “how can you expect the rest of the organisation to learn from it and the rest of society to learn where things have gone wrong?”

*The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP, is published by Pluto Press

25 September 2025

 

 

Darling accuses DWP of ‘absolutely shameful’ cover-up over Access to Work changes

The Department for Work and Pensions (DWP) has been accused of an “absolutely shameful” cover-up, after refusing to release documents that should show why disabled people across the country have faced cuts to their Access to Work support.

Disabled campaigners have been warning for the last 18 months of DWP cuts and inconsistent decisions on their Access to Work (AtW) claims.

But when social security and disability minister Sir Stephen Timms was challenged on these apparent cuts this summer, he insisted that no guidance had been issued to reduce support, and he said: “No changes have been made to Access to Work policy.”

In his response to a written parliamentary question from Liberal Democrat work and pensions spokesperson Steve Darling in July, he said instead that guidance was “now being more consistently applied” and that “work has been underway to improve [AtW] decision-making by applying the guidance with greater consistency, to provide a fairer process”.

He said: “This may mean that some awards change at the point of renewal, but there has been no change in Scheme policy, or instruction to reduce support levels.”

But Sir Stephen added: “Any updates to operational guidance are reflected through the published version available online at GOV.UK.”

Disability News Service (DNS) subsequently submitted a freedom of information request for DWP to provide all the changes to AtW “operational guidance” in the last 24 months.

But DWP has now replied to say that, although it holds this information, it would take more than three-and-a-half working days to determine “whether the Department holds the information, and locating, retrieving and extracting it”, so it is not obliged to seek the documents under freedom of information laws.

The DWP freedom of information team said this was because “the time period you have chosen is very wide and the topic you ask about is very broad” and suggested instead that DNS should “narrow your request to the latest version of a specific section of a particular topic within Access to Work that you are interested in”.

Speaking to DNS at the Liberal Democrat conference in Bournemouth this week, Darling said this lack of transparency from DWP was “absolutely shameful”.

He said: “We need to have that transparency about what is going on, because the evidence we have has demonstrated that there have been significant changes [to people’s AtW support packages].”

He said he was convinced that cuts were being enacted by DWP even if they were coming through operational changes rather than alterations in policy.

He told DNS that he has heard from disabled people made redundant from disability charities who have been offered much lower levels of support when they applied for AtW support with their new job.

He said: “What was taken as a given with their previous employment, [AtW] are shrinking it down, whether it’s travel to work or the level of support workers, or the way support workers are employed.

It is just absolutely perverse.

I’m sure there are cuts; there are cost savings happening there and I’m sure the Treasury are delighted with it being sucked back into the system.”

A consultation on the future of the AtW scheme has now closed.

Work and pensions minister Baroness Sherlock said, in a written answer to the disabled Liberal Democrat peer Baroness [Celia] Thomas earlier this month, that DWP was now “reviewing all aspects of the Scheme now that the consultation has closed”.

25 September 2025

 

 

Disabled activists working with peers to address serious flaws in ‘dangerous’ assisted dying bill

Disabled activists who are working with sympathetic peers to address the serious risks posed by the assisted dying bill believe there is also still a chance that the legislation could eventually be thrown out by the House of Lords.

Not Dead Yet UK (NDY UK) said there were grounds for “hope” after the completion of the first two days of debate on the terminally ill adults (end of life) bill in the Lords.

Friday’s debate saw speakers opposed to the bill outnumbering supporters by about two to one.

NDY UK said the campaign was “in the best place it could have been, because we can’t kill the bill at this stage.

While NDY UK continues to oppose the bill in principle, it recognises the need to engage with the legislative process to help ensure, if the bill does pass, it contains the strongest possible safeguards to protect disabled people.”

Almost two-thirds of peers who spoke during the debate on Friday (19 September) were opposed to the current version of the bill, while a little over a third were in favour, a similar proportion to the first day of the debate the previous Friday (12 September).

Of 15 Labour peers who spoke on 19 September, nine were in favour, five were against, and one – speaking for the government – was neutral.

But of 29 Conservative speakers, just seven were in favour and 22 were opposed to the bill in its current form.

Liberal Democrat peers were split, with two on each side, while of 11 crossbench speakers, five were in favour and six were against, while seven non-affiliated peers spoke against the bill and just one in favour.

George Fielding, a member of NDY UK’s coordinating group, who watched both days of the second reading debate from the floor of the Lords – as he is a wheelchair-user – said he was “genuinely moved by the quality of the debate, by the nature of the debate”.

He said NDY UK and other opponents of legalisation had formed “a hotchpotch alliance” among cross-party and crossbench peers.

He said: “We are building a network and a consensus across the Lords and I think that is emblematic of the fact that this bill will touch pretty much every corner of our society, and every corner of the House of Lords has people we have found are sympathetic to our views.”

Fielding said NDY UK was convinced that the bill would be “significantly amended” by peers “because the consensus is, at the very, very least, that this is a dangerous bill, it will foreshorten lives.

At the very least, this is going to be one of the most significantly-amended bills in parliamentary history.”

He said NDY UK was “working closely with cross-party peers and allies to propose amendments aimed at closing loopholes and reducing risks, especially around coercion, eligibility, and judicial oversight.”

Fielding said there was an “incredible effort going in the Lords” – with input from NDY UK – to make the bill safer through amendments, because it was currently “unworkable”.

NDY UK welcomed the decision on Friday to set up a select committee of peers that will take expert oral evidence from ministers, professional bodies and legal experts, which Fielding said would be “another public opportunity” for peers to probe the bill’s weaknesses and to “demonstrate how dangerous this bill is”.

He added: “NDY UK plans to contribute evidence and research to inform the committee’s understanding of how disabled people may be affected by the bill.”

This committee will hold six evidence sessions over three weeks, beginning in the week of 20 October.

The committee stage will then follow, with its clause-by-clause examination of the bill.

Among those who spoke in Friday’s debate was disabled Conservative peer Lord [Kevin] Shinkwin, who said the bill would “prise open” a “Pandora’s box” that would be “the stuff of nightmares”.

He said the bill “gives the state a licence to kill the wrong type of people.

I am the wrong type. This bill effectively puts a price on my head.”

He told fellow peers that, if the bill’s scope was expanded over time, he faced “the realistic possibility, as a severely disabled person, of being killed as a result of legislation passed by [the House of Lords]”.

And he pointed out that no organisation of or for disabled people supported the bill.

Another disabled Conservative peer, Lord [Craig] Mackinlay, who became disabled in 2023, said he had found the “joyous, tear-flecked celebrations” by some MPs when the “unwholesome” bill was passed in the Commons to be “quite bizarre and chilling”.

Among his concerns was the risk of coercion, and he told peers: “I am professionally trained and licensed to do probate work through the Institute of Chartered Accountants; believe me, post-death battles over inheritance can get very ugly.

I am fearful of the coercion of the elderly and the vulnerable. It is so obvious.”

Baroness [Luciana] Berger, a former Labour MP and minister, recalled her shock when hearing a constituent speak of wanting their family member dead.

She said she had also not forgotten “the words and realities of too many former constituents: people isolated and abused in their own homes, sometimes for decades, in fear for their own lives; people who felt like a burden because of long-term illness or serious mental health conditions, especially the elderly; and people treated as though their lives were worth less because they had a disability.

Many were from low-income backgrounds, facing not only poor health but the crushing stress of unaffordable care costs.”

She was another peer to point out that there was “no organisation of or for disabled people in this country that supports the bill”, and she added: “In considering who the bill might benefit by giving them more autonomy, we must equally consider who it may harm by taking their autonomy away.”

The former Conservative minister for disabled people, Lord [Mark] Harper, told fellow peers that many of the disabled people he had met as minister and shadow disability minister were “profoundly concerned by what the bill will do to society’s view of people who have challenges thrown in front of them”.

He said the bill was “not supported by a single organisation in this country that represents disabled people – not a single one – and we should listen to their views and take them very seriously”.

The Liberal Democrat peer Lord Beith said: “I have this fear – this instinct – that this is one of those big decisions that society may one day regret. There will be no way back.”

Lord Falconer, the Labour peer sponsoring the bill in the Lords, told fellow peers: “One of the features of this debate was the personal experience that so many people have had of how, had that option been available, it would have ended terrible suffering.

That suffering is not often about the pain but about the lack of dignity and the profound desire to keep control, because that is what people want.

I believe, from my own experience and from talking to so many people, that having that option is important.”

NDY UK argues instead – with many other disabled-led organisations – that the bill risks embedding discrimination into end-of-life law, “especially at a time when many disabled and terminally-ill people still struggle to access basic care and support”.

Lord Falconer also apologised for not declaring in the first day’s debate that he had benefited from an assistant funded by Bernard Lewis – founder of high street retail chain River Island and a supporter of legalisation of assisted suicide – to support him with his work on the bill, and that literature he had sent to fellow peers had been funded by the pro-legalisation organisation Dignity in Dying.

25 September 2025

 

 

UN calls for human rights assessment of government’s benefit cuts bill and mental health reforms

Disabled experts from the United Nations have told the UK government to carry out a “comprehensive” assessment of the human rights impact of its universal credit cuts bill, further plans to reform disability benefits, and its mental health reforms.

The UN’s committee on the rights of persons with disabilities (CRPD) had previously raised concerns about the impact on disabled people of the Universal Credit Act, the mental health bill, and further reforms laid out in March’s Pathways to Work green paper.

It wrote to the government after being alerted to the implications of its plans by DPO Forum England and the user-led, rights-based organisation Liberation.

Now, after assessing the government’s response, and evidence provided by disabled people’s organisations, the committee has called on the UK government to act.

It says it should assess the impact of its reforms, and ensure – in “close consultation” with disabled people – that its future plans do not cause any further “retrogression” in their rights, following years of attacks by successive governments.

The UN committee calls for a comprehensive human rights assessment of both the Universal Credit Act and Pathways to Work, before implementing the cuts and reforms to disability benefits expected in this autumn’s white paper.

And it calls on work and pensions ministers to take measures to “eliminate and reduce” the negative impact of the Universal Credit Act on disabled people, and to carry out a full assessment of its impact after its measures have been implemented.

It should then – again, in close consultation with disabled people – set out a plan to mitigate the impact of the act to ensure disabled people have access to the support they need to fulfil their rights to live independently, be included in the community, obtain work and have an adequate standard of living.

And it says that government plans to scrap the work capability assessment must be “designed and implemented” with the “close consultation and active involvement” of disabled people, and that they should not lead to any further assault on disabled people’s rights.

It calls for action to ensure, after months of concerns about Labour’s plans to force banks to carry out mass surveillance of claimants through its “Orwellian” public authorities (fraud, error and recovery) bill – currently approaching its final parliamentary stages – that those banks are not able to access claimants’ personal and private information.

The committee also calls for a comprehensive human rights assessment of the government’s mental health bill, which has been approved by the House of Lords and reaches the report stage in the Commons on 14 October, to ensure it is “fully aligned” with the UN Convention on the Rights of Persons with Disabilities (UNCRPD).

And it says the government should improve its procedures for measuring the impact of new laws on the rights of disabled people.

Rick Burgess, co-chair of DPO Forum England, said: “We are grateful to the UN for recommending the UK government make a full human rights assessment of the impact of its social security policies, introduce mitigations to protect us from further harm, protect us from bank spying, and remind the government they should be consulting closely with disabled people and our organisations.

It illustrates again that the UK government remains hostile to disabled people, and evades its treaty and legal obligations, but we will not relent in defending our rights and lives.”

Dorothy Gould, Liberation’s founder, said she was “absolutely delighted” that the committee’s response “cuts right through” the government’s attempts to justify its mental health bill, and she praised its “vital” intervention and “refutation of the government’s stance”.

She said the government’s earlier response to the committee had “utterly failed either to acknowledge the continuing, highly discriminatory nature of this bill, or to set out any plans for the fundamental changes that are needed” and had “misleadingly claimed” the bill was compatible with UNCRPD.

And she said it was a “complete disgrace” that the government had “yet again tried to justify the bill’s continuing treatment of people in acute mental distress and people with learning difficulties, or autistic people, as second-class citizens”, and had “again tried to argue that involuntary hospitalisation and forced treatment are not disability-based discrimination”.

Gould said the government was also still failing to make the committee’s Deinstitutionalisation Guidelines “its baseline for ensuring that we can instead live independently in the community, just like anyone else”, while also claiming it was making good use of consultation with user-led groups and individuals with lived experience “in the teeth of contrary evidence”.

Asked if the UK government accepted the committee’s recommendations, and if it would act on them, a DWP spokesperson failed to mention the recommendations in its statement, although it insisted the government was committed to implementing the convention.

In its statement, DWP said: “We’re changing the welfare system so sick or disabled people have the opportunities to move into good, secure work and out of poverty as part of our Plan for Change.

The views of disabled people remain at the heart of our decision making, including through the consultation earlier this year and the Timms Review, which will be co-produced with disabled people and their organisations.

Our reforms will rebalance the rates of universal credit to reduce the perverse incentives that trap people out of work, while giving people the genuine support they need through our £3.8 billion employment support package.”

Asked if the Department of Health and Social Care (DHSC) accepted the committee’s recommendations, and if it would act on them, a DHSC spokesperson also failed to mention the committee in its statement.

Instead, it said: “The Mental Health Act is there to protect people when they are at their most vulnerable, and in many cases, it has saved lives.

But it is hugely outdated and has not kept pace with evolving understanding of mental health, learning disability and autism.

Through our mental health bill, this government is now one step closer to bringing forward the essential reforms that will transform the care of some of our most vulnerable people, providing them with more dignity, choice and voice.

The 10 Year Health Plan sets out ambitious plans to boost mental health support across the country so people can access the right support at the right time in the right place.

This includes ensuring more people get the support they need in the community, closer to where they live.”

25 September 2025

 

 

DWP is ‘dysfunctional’ and needs major review, says Lib Dem Steve Darling

The Department for Work and Pensions (DWP) is “dysfunctional” and needs to be the subject of a major review, according to the disabled MP who speaks for the Liberal Democrats on work and pensions.

Steve Darling said his first year as an MP and as the party’s spokesperson had convinced him of the major problems within DWP and the “broken” social security system.

He said a review would need to engage with disabled people and others with lived experience of the benefits system, and academics, because the benefits system should be co-designed with claimants.

In an interview with Disability News Service at his week’s Liberal Democrat party conference in Bournemouth, Darling also raised concerns about the new work and pensions secretary, Pat McFadden.

He said McFadden appeared to be a “take no prisoners” and “driven” politician and an “enforcer”, and he raised concerns about his past comments about financial support for people with mental distress.

McFadden told Times Radio in March that he wanted benefit claimants with “mental health and depression and anxiety” to be “given support but not financial support”.

Darling also said that McFadden appeared to be a career politician who was lacking in “empathy and engagement and passion for people”, and that he seemed to be “a bit of a SPAD*-spawned apparatchik” who would “probably take no prisoners in driving forward with Starmer’s plans”.

He said he believed that the right-wing Reform UK was “worrying [the government] massively and I fear that they may lose their humanity for fear of Reform”.

Darling also said he had serious concerns about DWP forcing its disabled advisers to sign non-disclosure agreements (NDAs).

He said he and his wife had been forced to sign an NDA after winning a disability discrimination legal case and he said: “I really hate NDAs. They are meant to be there to protect intellectual property of commercial interests.

One of the things that we need to see change on is the culture of DWP and having a more open and transparent approach.”

He said that “slapping NDAs on those who they are engaging with” sends a “negative” message.

Darling also called for the Commons work and pensions committee to investigate the unreliability of DWP statistics on “economic inactivity”.

DNS reported last week that the proportion of working-age disabled people in England who are “economically inactive” was not “spiralling” and may even have fallen over the last nine years, according to new official government statistics.

The new figures came from the Office for Health Improvement and Disparities, just as a leading expert, Professor Ben Baumberg Geiger, from King’s College London, published a blog which showed that DWP’s “raw statistics” on all out-of-work benefits – not just relating to disabled people – were “wildly misleading”.

Darling said he was “keen to suggest” an inquiry by the work and pensions committee into the use of these statistics.

He said an investigation would “either debunk” the figures used by DWP or prove their accuracy.

He said: “My real fear is that, in our now Trumpian world, [the far right] don’t need the facts to add up to make outlandish claims.

The far right will just make up narratives for their own purposes and demonising others is part of their playbook and sadly people with disabilities and quite often people with hidden disabilities are in their crosshairs.”

He said that “unpicking” the claims and counter-claims behind the figures on economic inactivity should be “part of that push back against the far right that we need to be doing” because “otherwise that half-truth will be built on by the far right to demonise people with disabilities”.

*A SPAD is a ministerial special adviser

25 September 2025

 

 

Lib Dems insist they are still focused on social care, despite leader concentrating again on carers

Senior Liberal Democrat MPs have insisted they are still committed to social care reform and want to move towards eliminating all care charges, despite the party saying little or nothing about the issue during its annual conference this week.

Liberal Democrat leader Sir Ed Davey focused again on improving support for “family carers” – he is one himself – but said nothing in his main speech about disabled people who rely on care and support, other than saying he wanted to see a country that “properly values care” and one “where we take care seriously”.

He mentioned family carers like himself 10 times in Tuesday’s speech, without once mentioning the adult social care crisis, which sees tens of thousands of disabled people falling into debt every year because of care charges.

Last year, Disability Law Service published research which showed that disabled people across England were continuing to face unlawful discrimination and inequality on an “unparalleled” scale due to “unjust” social care charging policies.

Earlier in the conference, Dr Danny Chambers, the party’s mental health spokesperson, told Disability News Service (DNS) that he was in favour of moving towards free social care.

He said disabled people were “inadvertently sort of being punished for having a disability because of the changes in personal independence payment and all that kind of stuff, so if it ends up giving people more independence and allowing them to live a much more fulfilling life, it actually ends up costing the taxpayer less anyway.”

At last year’s general election, the party promised to offer free personal care to all adults, although it would not scrap charges for other support such as housework, shopping, laundry and engaging with the local community.

During a Health Foundation and Ipsos fringe event, Dr Chambers said the party was “absolutely focusing” on social care.

The Winchester MP said that, at any one time, the Royal Hampshire County Hospital in Winchester had between 160 and 200 people “who would be better off cared for with a social care package than stuck in a hospital bed”.

But, he said, it costs more than £850 a night to keep someone in a hospital bed and only a fraction of that to fund a social care package.

This may save a council money from its social care budget, he told the meeting, but “as a tax-payer, you don’t care which silo it comes out of, it’s costing us £850 a night to keep these hundreds of people in a hospital bed that don’t need it.

Our mantra has been, ‘You can’t fix the NHS without fixing social care.’”

He said his party had been “genuinely disappointed and quite annoyed” that the new Labour government had so far placed “so little emphasis on social care”, including in the NHS 10 Year Health Plan for England, and the NHS workforce plan, due this autumn, and extra funding provided to the NHS.

He said: “None of it is focusing on social care.

They are pouring money into a leaky bucket, and if you do not plug those holes it doesn’t matter how much money or how much you try and reform other parts of the NHS, it means there’s always going to be this huge drain that means you cannot unblock these huge problems.”

At a question-and-answer session, also attended by Dr Chambers, the party’s health and care spokesperson, Helen Morgan, told DNS that she came away from a cross-party roundtable meeting on social care reform feeling “reasonably optimistic”.

The long-awaited meeting was held to discuss the work of the government’s Independent Commission on Adult Social Care, which is chaired by the crossbench peer Baroness [Louise] Casey.

It was attended by senior representatives from the Labour, Conservative, Liberal Democrat, Green and Reform UK parties, including health and social care secretary Wes Streeting.

Asked by DNS whether she was encouraged by the attitudes of the other parties on social care, Morgan said on Monday that she came away feeling “reasonably optimistic”.

But she said she made clear in the meeting that the Liberal Democrats believed that the timetable set by the government, which will not see the commission produce a final report until 2028, was “too late”.

But she said: “At least we had that first discussion, and we had that opportunity to point out the urgency of delivering.

It was an introductory discussion; it was trying to find the points of similarity between the different manifestos.

I wouldn’t say there were any particular breakthroughs in the first discussion.

At least we had that first discussion, and we had that opportunity to point out the urgency of delivering.”

Dr Chambers said earlier in the week that the government’s decision to wait until 2028 for the commission’s final report suggested it was “playing for time”.

He said: “We don’t need to wait until 2028 to say something needs to be done and then start the process of implementing something.”

At another fringe meeting, hosted by the Liberal Democrat Disability Association (LDDA), Dr Katharine Macy, LDDA’s chair, called for the party to do more to focus on social care.

They wrote the young carers motion to the party conference in 2019 which kickstarted Davey’s focus on carers.

And they told the fringe meeting that the party’s public statements on care can sometimes suggest that disabled people are “a burden”.

Dr Macy, a disabled person and carer themself, said: “There are times when it has crossed the line. There are times when it very much skirts the line.”

They said their party needed to be aware that there were more disabled people than carers, although the emphasis in its public statements also reflected a culture where caring is seen as noble and being disabled is seen as being a burden “and that is where we can start to change things”.

Dr Macy said the party needed to address its focus on caring rather than social care, but that the Liberal Democrats needed to do that by saying more about social care rather than less about caring.

25 September 2025

 

 

New publications ask how disabled people and allies can hold the state to account for welfare state killings

A new series of resources examines ways in which disabled people and allies can find ways to hold the state to account for the deaths of hundreds – and probably thousands – of claimants it has killed through welfare state violence.

The three resources are being released as part of the Deaths by Welfare project at Healing Justice Ldn, which has previously created a timeline charting 30 years of evidence linking the systemic violence of the Department for Work and Pensions with the killing of countless disabled claimants of benefits through state violence.

The Deaths by Welfare project has also produced an exhibition, podcasts, and more than 50 interviews with disabled activists and bereaved family members.

Healing Justice Ldn hopes the new resources* – written by Dr China Mills – will inspire activists to find new ways to secure welfare justice and work towards new, “life affirming” systems of support.

The first resource to be published, Deaths by Design, asks whether the social security system was actually “deadly by design” rather than being a system riddled with flaws and mistakes by DWP staff.

It points to the coroner who concluded at the end of an inquest into the death of Philippa Day that there were systemic flaws in the personal independence payment system.

As disabled activist and author Ellen Clifford said in one of the Deaths by Welfare podcasts: “They created a system that’s deliberately designed to push people into poverty because our lives are worth less to them than other people’s.”

And it quotes fellow disabled activist Rick Burgess, in another Deaths by Welfare interview, who said: “We’re now 14 years into this process; that’s not an accident, that’s not a passing fad – that’s a cultural democide against a demographic, that demographic being disabled people benefit claimants.”

Deaths by Design asks the question: “If systems are harmful by design then we need to campaign beyond ‘cuts’.

If we only mobilise around ‘cuts’ to welfare, we might overlook how harmful the foundation of welfare can be.”

And it concludes: “People want to build a different welfare system but it’s hard to get specific about what we want… when all we’ve known is a violent bureaucratic system.”

Another of the resources, Evidence, examines how disabled people and bereaved fam­ilies have produced evidence of state harm; how to use that evidence in ways that do not dehumanise disabled people; and how disabled people have used direct action to alert the public to this evidence.

It points out that constantly being asked to provide evidence of the harm the system is causing “mirrors the violence” of claimants being forced to prove they are disabled so they can receive the support they need to survive.

One of the questions it asks is: how many people must die through DWP violence before those in power listen and act?

The third resource, Accessing Justice, co-written by Dr Mills and Imogen Day – whose sister took her own life due to DWP’s actions and failings – examines how families bereaved by DWP killings have sought justice.

It looks at the experiences of relatives Joy Dove, Alison Burton and Imogen Day – each of them disabled people themselves – after the deaths of their daughter, father-in-law and sister through DWP violence.

It also hears from the mothers of Seni Lewis and Komang Jack Susianta, who were both killed by non-DWP state violence.

While Accessing Justice accepts that some activists want to see those guilty of complicity in the state killings face criminal justice, HJL also questions whether justice for those killed can ever be secured through the criminal justice system, and whether there are other ways of holding those responsible accountable.

*DNS editor John Pring was involved in editing the resources and was co-editor of the Deaths by Welfare timeline

25 September 2025

 

 

Mother left ‘disgusted’ by DWP’s silence over secret report into Jodey Whiting’s death

The Department for Work and Pensions (DWP) has refused to release any information about a secret report into the death of a disabled woman, despite a coroner ruling that its actions had been the “trigger” for her suicide.

DWP has even refused to tell lawyers for the family of Jodey Whiting whether it carried out an internal process review (IPR) into her death.

It claimed in the letter that releasing an IPR to her family could breach her privacy, even though she died more than eight years ago.

It said IPRs were “internal retrospective investigations focused on organisational learning, not public accountability” and that they “often contain sensitive personal information about claimants, including health, benefit history, and interactions with DWP staff”.

It added: “The disclosure of such information, even to close family members, could be considered a breach of privacy.”

Disability News Service (DNS) reported in June that a second inquest into Jodey Whiting’s death – which only happened because of her mother’s eight-year campaign for justice and accountability – found that her “deteriorating” mental health had been “precipitated” by the withdrawal of her out-of-work disability benefits after she missed a work capability assessment.

But DNS also showed in June how DWP hid the truth from the coroner about its role in Jodey Whiting’s suicide, including by failing to confirm if an IPR was carried out.

Joy Dove, Jodey Whiting’s mother, told DNS this week that she was “really disgusted” by DWP’s refusal to release the IPR – or even to say whether one was carried out – after campaigning for more than eight years to discover the truth about DWP’s role in her daughter’s death, and for justice for her and countless other disabled people whose deaths were caused by DWP.

She said: “We were forced to give documents to the coroner, we had to do what we were told, so why the heck can’t they?

What’s the problem? We know she’s dead because of them. What are they hiding?

They don’t care. To them, Jodey is just a number. It’s not personal to them. They are not bothered.”

In the letter, a solicitor in the Government Legal Department – writing on behalf of DWP – made it clear that DWP “fully accepts the coroner’s conclusions” in the second inquest, and “accepts that the withdrawal of Jodey’s Employment and Support Allowance precipitated her deteriorating mental state”.

But further anguish was caused to the family by the Government Legal Department mis-spelling Jodey’s name in a brief one-line apology included in the letter, saying: “Please do pass on this heartfelt and sincere apology from DWP to Jodie’s family.”

Dove said she was annoyed at this lack of care and respect and said she did not consider it a “proper apology”.

She is now considering a complaint to the Parliamentary and Health Service Ombudsman over DWP’s actions and its role in her daughter’s death.

The letter came as Steve Darling, the Liberal Democrat work and pensions spokesperson, told DNS that he was hoping to use the government’s new Hillsborough Law to force DWP to release IPRs to relatives.

This is because Labour’s public office (accountability) bill includes a new legal duty on public authorities and public officials “to act with candour, transparency and frankness”.

In an interview with DNS at his party’s annual conference in Bournemouth, Darling said he wanted the bill to produce a “culture change” within DWP and the whole of Whitehall, and that he intends to ask parliamentary questions on how the release of IPRs will be part of that.

The solicitor for Jodey Whiting’s family, Merry Varney, from Leigh Day, said yesterday (Wednesday): “Joy has fought for many years to secure recognition that Jodey’s death was caused by DWP failings.

The second inquest into Jodey’s death confirmed that earlier this year and during the hearing the DWP witness was unable to confirm whether an internal process review had been competed following Jodey’s death.

Joy had hoped that a full and frank apology, together with disclosure of information about any internal process review, would come from the DWP.

The response indicates a continued unwillingness of the DWP to be fully transparent and to admit, in clear unequivocal terms, that their acts and omissions cause deaths.”

A DWP spokesperson said: “We continue to offer our sincerest condolences to Jodey Whiting’s family and are deeply apologetic for the misspelling of her name.”

The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP, including Jodey Whiting’s, is published by Pluto Press

25 September 2025

 

 

Anger and frustration after DWP’s latest jobcentre announcement and McFadden’s ‘incentives’ comment

Sick and disabled people have raised serious concerns about the latest Department for Work and Pensions (DWP) announcement on its strategy to persuade more claimants receiving out-of-work sickness and disability benefits to consider moving towards employment.

Many reacted angrily to DWP’s announcement that every jobcentre in England, Scotland and Wales now has “specialist” Pathways to Work advisers who will offer skills and employment support to claimants receiving out-of-work disability benefits.

DWP said it has redeployed 1,000 existing jobcentre staff to provide voluntary help to people on universal credit who have “no requirement to look for work or engage with job help because of their condition”.

Disabled people highlighted concerns this week about safeguarding and the lack of evidence for such a strategy, and they questioned why a Labour government did not do more to focus on cutting NHS waiting-lists and addressing barriers in the workplace.

Their anger and frustration only increased when new work and pensions secretary Pat McFadden claimed in an interview that there were currently “incentives” in the system for people to declare themselves unfit for work so they can “double their money”, and also claimed that people were “declaring themselves long-term sick”.

McFadden will have been aware that claimants cannot declare themselves “long term sick” but instead must go through the harsh work capability assessment process in order to be found not fit for work, and he should also have been aware that this system has led to countless deaths.

Researcher and writer Sue Jones responded on X/Twitter: “Progressive, incurable illnesses are not ‘perverse incentives’ you vicious man, and no amount of lying about people and inventing ‘incentives’ and motives will change the fact that many of us can no longer work, simply because we are too ill and disabled.”

DWP said it hoped its Pathways to Work advisers would help 65,000 people found to have limited capability for work and work-related activity (LCWRA) by the end of 2025-26.

DWP claimed this kind of “additional work coach support” was “proven to help people into work” and that research had found LCWRA claimants who accepted this support were a third more likely to be in work a year later.

However, the research it referenced, published by DWP in March*, showed the proportion of those in the LCWRA group in work rose from just eight per cent to 11 per cent, a year after the provision of “additional work coach support”.

The department said more than 10,000 people had taken up the voluntary offer and had had at least one appointment since April 2025.

It said it would not contact claimants with “the most severe and lifelong health conditions” – which DWP later confirmed will match the “severe conditions criteria” described in schedule one of the new Universal Credit Act – or those who receive support through the “special rules” for those with less than 12 months to live.

But there was significant concern among sick and disabled people on social media after the announcement.

Disabled People Against Cuts said on its Facebook page: “The question that’s in the back of our minds is, how long before it’s mandatory?”

Many warned that even a voluntary approach would cause serious safeguarding issues.

The anti-cuts grassroots group Disability Rebellion said on X/Twitter: “Here we go again – DWP are now going to ask thousands of UC claimants with no requirement to look for work to attend ‘work conversations’.

No thought given to safeguarding or how unwell this could make people.”

Another grassroots group, Recovery in the Bin, said: “We don’t need f*****g skills. We need healthcare, housing, enforceable legal rights.

Want to improve disabled people’s access to work? Make legal aid more widely available for disability discrimination cases.”

Others pointed out that such initiatives “barely make a dent in employment rates”, because the reasons sick and disabled people are not in work are not “lack of coaching, confidence, etc”.

Many suggested that the government would do better to focus on improving access to NHS services and investing in treatment for conditions such as long Covid and ME, and addressing discrimination by employers.

Similar points were raised by those who said the barriers they faced were not those that could be addressed by DWP Pathways to Work advisers.

One of those who responded to the announcement said: “I worked for Goldman Sachs, UBS, Deutsche Bank, Standard Chartered, etc over the course of my career.

I do not need more skills or experience. I am TOO ILL to work.”

Another said: “I’m chronically ill and mostly bedbound. I’m a fully skilled plater/welder.

I also have qualifications in carpentry, hedge laying, dry stone walling, and also have chainsaw licence to fell medium sized trees.

My problem isn’t skills. It’s illness.”

*DWP did not provide a link to this research in its press release

25 September 2025

 

 

Other disability-related stories covered by mainstream media this week

MPs have warned the Government of a “showdown” over reforms to the special educational needs system they fear will cut support for disabled children. Labour members say they are gearing up to vote against any changes that “take away services” or “reduce support, financial or otherwise” for pupils with special educational needs and disabilities. Backbenchers say their red lines would also include children losing their legal rights to funding and provision – currently set out through education health and care plans: https://inews.co.uk/news/education/starmer-collision-course-mps-send-reforms-austerity-3930632

Trafford Council’s new council tax reduction scheme must be quashed after a high court judge ruled it unfairly discriminated against two “vulnerable” residents who discovered they had to pay the full bill when previously they had to pay nothing because they were on benefits. A judge ruled the council’s working-age local council tax reduction scheme for 2025-26 was both unlawfully adopted and discriminatory against disabled people and carers on certain benefits: https://www.manchestereveningnews.co.uk/news/greater-manchester-news/high-court-slams-obviously-unfair-32514179

More than 1,000 disabled children across the UK are waiting for wheelchairs and mobility equipment that could transform their lives, according to charity Whizz Kidz. The charity, which helps wheelchair-users up to 25 years old, has been forced to close its specialist wheelchairs waitlist for the first time in its 35-year history. It says escalating costs and squeezed NHS budgets are creating a “huge demand” for its service, leading to long delays: https://www.bbc.co.uk/news/articles/cm2zwm8m41mo

25 September 2025

News provided by John Pring at www.disabilitynewsservice.com

 

Sep 132025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Calls for an independent PIP review with UK minister under fire

A Welsh disability group is calling for an independent review of Personal Independence Payments (PIP).

Disabled People Against Cuts Cymru (DPAC Cymru) has accused the disability minister Stephen Timms of failing to properly lead his own review into the disability benefit, saying that “co-production is not taking place as promised.”

Speaking exclusively to LBC’s Welsh Correspondent Caitlin Parr, the group’s comments follow the Minister of State for Social Security and Disability, Sir Stephen Timms MP, meeting with the Welsh Government Disability Equality Forum on Tuesday 2nd.

LBC news reported that DPAC Cymru had long fought for disabled people’s voices to be heard in changes to welfare reforms, but were concerned that the minister, despite promises to engage widely over the summer, had so far left Welsh disabled people out of discussions around the review, outside of those forum meetings.

DPAC Cymru claims that Timm’s attendance at those recent forum meetings is “far too little and far too late for Welsh disabled people after months of stonewalling from Timms,” and said they were frustrated by “more promises but no action.”

Ben Golightly, from Swansea, is a coordinator for DPAC Cymru. He told LBC, “he [Timms] agreed in that meeting that it was important for Welsh disabled people and Welsh disabled people’s organisations to be heard. He was meant to talk about how he was delivering co-production. It was his job to do it. And he had no real update, because he hasn’t been doing that job.”

Despite promises from government ministers, DPAC Cymru say that co-production has not taken place, and they are “back to square one.”

Ben said, “We had hoped that after a major defeat in parliament that when he [Timms] promised co-production with disabled people, that we wouldn’t have to go through all of this again. There is so little trust in the way the government has treated disabled people that we need an independent review, led by disabled people, and Stephen Timms and the government should turn up and listen, but they should have no say over how it’s run because they’ve shown, throughout several months, that they’re unable to do it.”

Lee Ellery, an independent disability activist and lead press coordinator for DPAC Cymru, who has Cerebral palsy quadriplegic, agreed, telling LBC news it’s time more Welsh voices were heard.

Lee said, “people with disabilities, particularly in Wales, are left to the bottom of the pile so to speak, and we should be at the forefront of everything. I’m worried about what the result of the [PIP] review might come out to say, if the person who’s leading it doesn’t understand the whole process.”

LBC news reported that “the Timms review into PIP assessments is expected to conclude in Autumn 2026, when changes already decided on for new PIP claimants will come into force.”

DPAC Cymru’s calls for an independent review, made in an open letter released last Monday, has already received wide support, collecting 600 signatures and the support of representatives of more than twenty-five organisations.

Comments collected from respondents talk about their feelings of hurt, being “belittled,” “completely disregarded and isolated,” and the “harm and loss of trust” caused by Timms and the government.

Signatures on the open letter are open until the end of September.

Sign here

A notice graphic with a red tinted photograph of Stephen Timms as the background. Title text to the left of him reads: "We want an independent PIP review" with emphasis on the independent. A divider then separates the next header text that reads: "Nothing about us, without us!", followed by another divider. Body text then reads: "Please sign and share our open letter!" with an arrow pointing to a link: "bit.ly/independent-pip-review". The DPAC Cymru logo sits at the bottom of the screen.
Sep 012025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The words "We want an Independent PIP Review" in bold and black text, with Independent highlighted in red. On the left there is a tear-out effect of a greyscale photo of a disability protest, and a red-tinted photo of Stephen Timms, the disability minister.

This is an open letter from DPAC Cymru, produced with feedback from six Disabled People’s Organisations.

Disclaimer: DPAC Cymru didn’t have time to reach 100% agreed wording with DPAC UK, as we would have liked to. Even within DPAC Cymru, the letter wording is somewhat of a compromise. However, for important tactical reasons in Wales, we felt it was important to publish without delay. DPAC have therefore agreed to share the letter with this disclaimer.

Click here for the Easy Read version.

To:

The Welsh Government,

The Scottish Government,

The Northern Ireland Executive,

The UK Government,

1st September 2025

After a major, if partial, defeat in parliament over disability cuts, the disability minister Stephen Timms promised MPs that the PIP benefit review would be co-produced by disabled people and their organisations.

There is widespread skepticism if this will genuinely be the case. Promises to “engage widely over the summer” have not been met, and there has been no transparency over Timms’ plans for “ten people” to have “a lot of sway”. His comments reveal that he does not understand what co-production means. Timms has also repeatedly declined to acknowledge the many serious failures of the Pathways to Work green paper consultation process, particularly felt in Wales.

We counterpose this to the Disability Rights Taskforce, initiated in partnership with the Welsh Government, which brought together 350 stakeholders and 200 policy experts, as a model of what co-production can look like. However, many Taskforce participants were frustrated that much of their work was ultimately missing from the Welsh Government draft plan. This is a lesson that even co-produced policy will fall flat without accountability. Disabled people’s organisations must be given the necessary resources and powers to carry out the implementation and monitoring of decisions.

[Some of us] cautiously welcome[d] the announcement of the Government’s new Independent Disability Advisory Panel. This panel is separate to, but will feed into, the Timms review of PIP. However, trust remains very low, and the terms – of “up to 10” people – have already been set for us. [See update, below]

We the undersigned demand that:

• The new Independent Disability Advisory Panel must be genuinely independent, representative, transparent, and have real powers of oversight.

• The UK government must acknowledge its failures in delivering the Pathways to Work consultation and legislative process, as a precondition to rebuilding trust and ensuring those mistakes are not repeated.

• The PIP review must be independently led by disabled people and our organisations, inviting the views of carers, volunteers, and workers in health, social care, housing, transport, and welfare.

• Any review of welfare reform must also, in a process led by disabled people, involve trade unions as democratic organisations representing 1.4 million disabled workers as well as representing the workers responsible for the day-to-day delivery of services that disabled people rely on.

• The scope of the PIP review must be widened to all aspects of welfare and employment for disabled people, guided by the principle: from each according to their ability, to each according to their need.

• Dedicated funding must be provided to Disabled Peoples Organisations to support outreach, accessible engagement, and the collection of views from disabled people, including those without internet access or digital skills.

• The devolved governments of Wales, Scotland, and Northern Ireland, and councils, should recognise and support this independent review even if the UK government refuses to.

• The UK government must immediately halt all cuts to disability and incapacity benefits for the duration of the review, and urgently fix Access to Work.

• Parliament must be given time to properly scrutinise any new legislation.

• The UC bill should be repealed. It is flawed, and was rushed through in an abnormal and undemocratic way.

 

[Update 4th September] Statement from DPAC Cymru regarding the “Independent Disability Advisory Panel”:

“The recently published terms for the so-called Independent Disability Advisory Panel, including the requirement to sign a non-disclosure agreement, are completely unacceptable. We are going to go back to a full consultation with all of our members and allies and take time for discussion to correct the weakness in our compromise wording of ‘cautiously welcome’ and come back united, realigned on the strongest possible response. We hope you will continue to support the demand for an independent PIP review, led by disabled people, and support this letter with your signature.”

 

For a full list of signatures and footnotes, see here.

To add your support to the letter, add your signature here

Here are short URLs for sharing the letter:

Non-Easy Read: Bit.Ly/independent-pip-review

Easy Read: Bit.Ly/easy-read-independent-pip-review

Aug 222025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

From Merseyside DPAC:

 

Join Disabled People Against Cuts to protest against the Labour policies killing disabled people outside the Labour Party conference in Liverpool 29/09/2025 at 12pm. We will assemble near the Wheel of Liverpool on Keel Wharf L3 4FN.

We encourage those who can to a mask in order to protect immunocompromised members of our community and will have some masks available for those who do not have their own. We ask that political parties do not bring branded placards.

#GenocideAbroadDemocideAtHome #WelfareNotWarfare

 

"Text over a dark background with the disability pride colours. Text reads "Genocide abroad, democide at home is Labour policy. 12:00 September 29th, the Wheel of Liverpool L3 4FN"

Beneath the text is an inverted black triangle with the text "DWP stop killing us" and a black and white photo of a group of protesters with a Merseyside DPAC banner.

Jul 032025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Disastrous’ cuts bill that leaves legacy of distrust and distress ‘must be dropped’ 1

Four disabled Labour MPs stand up to government over cuts to disability benefits 4

Silence from MP sister of Rachel Reeves over suicide linked to PIP flaws, just as government was seeking cuts 7

Disabled people receiving care were ‘ignored by design’ during the pandemic, Covid inquiry hears 9

Disabled activists warn Labour MPs who vote for cuts: ‘The gloves will be off’ 12

GB News says it has nothing to apologise for, after guest suggests starving disabled benefit claimants 15

SEND inspections find services in just one in four areas usually lead to ‘positive’ outcomes for disabled children 17

Other disability-related stories covered by mainstream media this week 19

 

Disastrous’ cuts bill that leaves legacy of distrust and distress ‘must be dropped’

Disabled activists have called on the government to scrap its “dangerous” and “disastrous” disability benefits bill, despite forcing ministers into last-minute changes that scrapped all their planned cuts to personal independence payment (PIP).

Chaotic events in parliament on Tuesday, and three months of activism since the publication of the Pathways to Work green paper, have left disabled people’s organisations (DPOs) appalled, shocked, and struggling to trust the government.

Their activism, together with the efforts of a small group of backbench MPs, forced ministers into a series of U-turns and concessions on the universal credit and personal independence payment bill.

The lack of trust in the government, and in the minister for social security and disability, Sir Stephen Timms, now creates a significant barrier as he begins a year-long review of personal independence payment (PIP), including an examination of its eligibility criteria and assessment process.

A chaotic few hours in parliament on Tuesday led eventually to ministers withdrawing all their proposed cuts to PIP, at least until the end of the review next autumn.

The bill passed its second reading by 335 to 260 votes, and it will return to the Commons on Wednesday (9 July) for its committee stage, with significant cuts to the health element for most new claimants of universal credit from next April remaining in the legislation.

Disabled people’s organisations were united yesterday (Wednesday) in their call for the “sham of a bill” to be dropped, with many expressing distrust in the government.

And there was little celebration that their successful activism – led by Disabled People Against Cuts (DPAC) and other grassroots groups such as Taking the PIP – had forced the government into gutting its bill.

DPAC described the bill as a “complete and utter mess”.

Paula Peters, a member of DPAC’s national steering group, said the process had done nothing but “cause more anxiety and more distress for disabled people”. 

She told Disability News Service (DNS) that she did not trust Sir Stephen as he had “shown time and again he doesn’t listen to charities, DPOs or disabled people”.

And she pointed to the concerns – expressed also by some MPs – that the government will merely introduce a new series of cuts to PIP at the end of the review, through a parliamentary mechanism that means they will not need to be approved by MPs.

Svetlana Kotova, director of campaigns and justice at Inclusion London, was also distrustful of the government’s motives.

She said: “The social security system needs reform, but not like this.

It is clear that this was never about reform, it was about balancing the books at the expense of disabled people.

Removing PIP cuts from the bill is a positive step, but there is no guarantee the government will be open to true co-production; more likely, they will want us to engage in ‘co-producing cuts’.

The bill still includes deeply harmful cuts to universal credit.

The government should admit they made a mistake, drop this harmful bill and go back to the drawing board.”

National Survivor User Network (NSUN) said the decision to gut the bill was “the direct result of tireless campaigning by disabled people and their organisations in recent weeks”.

But it said that the chaotic and confusing way it was passed showed “callous disdain for the lives of disabled people”, while the bill “should have been withdrawn in its entirety”.

An NSUN spokesperson said: “It is vital that co-production through the Timms review meaningfully involves disabled people, putting power in the hands of those whose lives will be most impacted.

We have seen the violence of the government’s rubber-stamp consultations so far and demand genuine co-production rather than inadequate and tokenistic consultation on an already-decided course of action.”

And it said the refusal to remove the cuts to the health element of universal credit for most new claimants from the bill showed the government “remains willing to attack disabled people” and was “a shameful attempt to divide the disabled community and stifle solidarity”.

The NSUN spokesperson added: “We will continue to organise with DPO allies, push for the rights-based reform which our deadly social security system needs, and ensure there are electoral consequences for those who go after disabled people in this way.”

Disability Rights UK (DR UK) said disabled people would be “enormously relieved” that the PIP cuts had been dropped from the bill, although “serious concerns” remained about the cuts to the health element of universal credit for most new claimants, which would make hundreds of thousands of the poorest people in the country even poorer.

A DR UK spokesperson said: “We’ve known all along that the public, disabled people and our organisations have found this bill to be unjust and unfair.

Yet the government has used every tool in its arsenal, every procedural trick, to push this dangerous bill through.”

DR UK said the government’s “floundering and chaos” was “a direct result of the steadfast work of disabled campaigners and our allies, who have made it clear that this bill is unworkable.

Despite attempts to silence us, through our collective campaigning, we made them drop billions of pounds worth of cuts, and we will continue to resist this disastrous bill.”

Rick Burgess, campaigns lead at Greater Manchester Coalition of Disabled People, said Tuesday’s events had demonstrated the “arrogance and disrespect” of the government, and he also called for the bill to be scrapped.

He said the bill still contained cuts to the health element of universal credit, and it imposed “extremely restrictive” criteria on those who will be offered some protection through the “severe conditions criteria”.

He said disabled people would seek to stop these elements of the bill through amendments.

Burgess added: “The PIP review must be to a specified standard of coproduction agreed with our organisations and be subject to statutory public consultation.

Given our experience to date, however, we have low confidence in the government.

However, it must also be said, while we lost the vote, we won a victory in gutting the bill and exposing the utter shambles of Starmer’s administration.”

The grassroots, user-led mental health group Recovery in the Bin (RITB) delivered a bleak assessment last night of the impact of the government’s actions.

An RITB spokesperson told DNS: “The whole sequence of events from the announcements, to constant vilification in the media, and from ministers, especially Kendall and Timms, has caused such distress that Labour have ended any hope of support.

They are loathed and despised, and we have no trust whatsoever in them not to attack us.”

AJ Le Brun, a disabled activist with DPAC Cardiff and Valleys, said the bill had been “rushed through” with no thought for disabled people.

She said: “The changes and promises made in the final hours before the vote may have soothed the consciences of some MPs, but we see through these shaky promises.

The changes to universal credit will push more of us into poverty, when we are already struggling with the rising costs of aids and support needed to live with dignity.

I do not trust Stephen Timms and his department to conduct a fair PIP review.

They have shown us they are not listening to disabled people by only providing one face-to-face consultation for Wales, and holding the vote the day after the consultation formally closed.

What confidence can we have that this review will be any better?”

Because of the number of changes to the original bill, DNS asked DWP to confirm exactly what the bill would now do.

Here is the list provided by the department (edited for clarity by DNS):

  • The bill will make changes to universal credit (UC) from April 2026
  • It will not bring forward any changes to the PIP eligibility criteria

From April 2026:

  • The standard allowance of UC will rise above inflation in each of the next four years
  • The health element of UC for new claimants will be reduced to £50 per week
  • Existing claimants of the health element and those new health element claimants meeting the severe conditions criteria (SCC) or considered under the special rules for end of life (SREL) will see their UC standard allowance combined with the UC health element rise in line with inflation in the next four years
  • People in the SCC group will be exempt from future UC reassessments

3 July 2025

 

Four disabled Labour MPs stand up to government over cuts to disability benefits

Four disabled Labour MPs stood up to their government’s attempts to reduce vital disability benefits, despite ministers’ chaotic last-ditch concessions to rebels that removed a significant chunk of their cuts bill.

Marsha de Cordova, Marie Tidball and Emma Lewell all voted against the universal credit and personal independence payment bill, and each of them delivered powerful speeches in the House of Commons on Tuesday.

Another disabled Labour MP, Marie Rimmer, also voted against the bill.

But a fifth disabled Labour MP, Vicky Foxcroft – who had played a key role in the rebellion that forced a series of government concessions – voted for the bill and its significant cuts to the health element for many new claimants of universal credit.

She and many other Labour MPs who had previously opposed the cuts bill voted with the government after the minister for social security and disability, Sir Stephen Timms, suddenly announced at 5.25pm on Tuesday – nearly four hours after the debate began and just 95 minutes before MPs voted – that there was to be another concession.

Ministers had already announced that existing PIP claimants would not now be subjected to new rules that meant they would have to be awarded at least four points on at least one “activity” to qualify for the PIP daily living component, which were to be introduced from November 2026.

Work and pensions secretary Liz Kendall had also announced the previous day that the government would no longer freeze the health element top-up for existing claimants of universal credit, and that they and new claimants who were terminally-ill or were placed in the “severe conditions group” would instead see the combined value of their universal credit standard allowance and health top-up “rise at least in line with inflation”.

But in a dramatic intervention, Timms then also announced at 5.25pm that no cuts at all to PIP would go ahead until his own review into PIP – which Kendall said would be “co-produced with disabled people, their organisations, clinicians, other experts and MPs” – was completed in the autumn of 2026.

This final concession ensured that the bill passed by 335 to 260 votes.

The committee stage of the bill will take place in just a few days, on Wednesday (9 July), but without any measures to cut PIP.

Marsha de Cordova, a former shadow minister for disabled people, was one of the few MPs in the debate to warn how previous Department for Work and Pensions (DWP) cuts and reforms had led previously to the deaths of many disabled people.

Speaking before the final concessions were announced, she pointed to the many internal process reviews into deaths linked to DWP actions, and the long-delayed second inquest into the death of Jodey Whiting, which found last month that DWP’s decision to wrongly stop her benefits after a string of safeguarding failings was the “trigger” for her to take her own life.

De Cordova told fellow MPs: “I set that out because it is important that we understand that disabled people’s lives have not been valued or respected for the last 14 years.”

She also pointed to the findings of the UN committee on the rights of persons with disabilities, which last April found successive Conservative-led governments had made “no significant progress” in the more than seven years since a finding of “grave and systematic” violations of the UN disability convention.

Marie Tidball delivered an emotional speech, in which at times she appeared close to tears, in which she told MPs she would be voting against the bill “with a heavy, broken heart”.

She said she had been in discussions with ministers since April, “making clear that I could not support the proposals on PIP”.

She added: “PIP is an in-work benefit designed to ensure that disabled people can live independently.

Low-level support such as PIP helps to build the bridge to the deinstitutionalisation of disabled people, keeping us out of the dark corners of hospitals, prisons and social care settings.”

Tidball voted against the bill despite the late concession from Sir Stephen Timms that ruled out all PIP cuts until the end of his review.

Emma Lewell also voted against the bill, despite the late concession.

She had told MPs that past Conservative social security reforms had not led to any cost savings but instead to “an increase in poverty, an increase in suicides, strain on the NHS and other public services, and, in the long run, higher welfare spending and reduced growth”.

But two other disabled Labour MPs, Liam Conlon and Jen Craft, voted for the bill, although they did not speak during the debate.

Steve Darling, the disabled Liberal Democrat MP and his party’s work and pensions spokesperson, voted against the bill, as did the rest of his party.

He had told MPs: “We all know that rushed bills are poor bills, and the law of unintended consequences will come to haunt the government if this bill goes through.”

Rachael Maskell, who was among leaders of the rebel Labour MPs – and proposed an amendment that would have killed the bill, but was defeated by 328 to 149 votes – told MPs in another passionate speech that she was voting against the bill because it was “a matter of deep conscience, as it should be and will be for us all”.

She was another MP who highlighted the harm caused by previous cuts and reforms to disability benefits, pointing to the 600 suicides between 2010 and 2013 that were linked to the programme to reassess incapacity benefit claimants.

Maskell said: “When they are managing discomfort, despair, pain and prejudice, are isolated and lonely, or their life has spiralled out of control, disabled people want anything but this bill.

They are already discriminated and dehumanised, so I plead that we do not leave them desperate, too.”

There was disappointment among many disabled people that among those voting for the cuts to the universal credit health element was Labour’s Debbie Abrahams, chair of the work and pensions committee, who had been outspoken about her concerns about the “dog’s breakfast of a bill”.

She had told MPs that “too many people relying on social security support to survive have died through suicide, starvation and other circumstances exacerbated by their poverty” in the last 15 years as a result of the “punitive, even dehumanising, social security system in which not being able to work has been viewed with suspicion or worse, with devastating consequences”.

But she still voted for the bill, despite its significant cuts to the rate of universal credit that will be paid to most new recipients of the health element of universal credit from next April, who will see the health element nearly halved and then frozen.

Asked last night (Wednesday) why she had voted for the bill, despite the significant cuts to disabled people’s support that it still contains, Vicky Foxcroft referred Disability News Service to a statement on her website.

She did not mention those cuts in the statement, but she said that securing the concessions was “a huge victory for Labour backbenchers” and that she voted for the bill because it was “now in a much better form than it was two weeks ago”.

She said she would only vote for the bill at its final Commons stage “if the final proposals reflect the commitments ministers have made”, and that she would be “looking for ministers to take these commitments forward and ensure we have co-production right across government”.

Because of the number of changes to the original bill, DNS asked DWP to confirm exactly what the bill would now do.

Here is the list provided by the department (edited for clarity by DNS):

  • The bill will make changes to universal credit (UC) from April 2026
  • It will not bring forward any changes to the PIP eligibility criteria

From April 2026:

  • The standard allowance of UC will rise above inflation in each of the next four years
  • The health element of UC for new claimants will be reduced to £50 per week.
  • Existing claimants of the health element and those new health element claimants meeting the severe conditions criteria (SCC) or considered under the special rules for end of life (SREL) will see their UC standard allowance combined with the UC health element rise in line with inflation in the next four years
  • People in the SCC group will be exempt from future UC reassessments

3 July 2025

 

Silence from MP sister of Rachel Reeves over suicide linked to PIP flaws, just as government was seeking cuts

Labour’s chair has refused to answer questions about a disabled constituent whose suicide was closely linked to flaws in the personal independence payment (PIP) system, just as her government was trying to cut PIP spending by billions of pounds a year.

Three months after an ombudsman found that failings within the Department for Work and Pensions (DWP) and its PIP system were a factor in the death of Tracie, from south London, her MP, Ellie Reeves, is still refusing to comment on that report’s findings.

Reeves is chair of the Labour party and a Cabinet Office minister, but she is also the sister of chancellor Rachel Reeves, who many disabled people blame for the government’s decision to attempt to slash spending on PIP and other disability-related benefits.

The ombudsman’s ruling was delivered to Tracie’s husband, Mustapha, just five days after Rachel Reeves announced, at the spring statement, that she would be making cuts to PIP spending of £4.5 billion a year by 2029-30.

It was Ellie Reeves, the MP for Lewisham West and East Dulwich, who referred the case to the Parliamentary and Health Service Ombudsman in December 2021, when Labour was still in opposition, and her office has supported Mustapha for nearly five years.

But since the ombudsman finally produced its report in March, Mustapha has not yet been able to discuss its contents with his MP.

He was originally told that Reeves was happy to discuss the report but had not yet received a copy, so he visited her office last month and posted a hard copy through the letterbox after an emailed copy apparently did not reach her.

Her office claims it did not receive a copy of the report until 18 June.

The ombudsman has apologised for not sending her a copy on publication, as it usually would; it finally emailed her a copy this week, but it is not clear why her office did not attempt to secure a copy of such an important report herself.

A member of her casework team has now told Mustapha that she – although not the MP – would be happy to discuss the report with him.

Mustapha has provided permission to Ellie Reeves to discuss the case with Disability News Service (DNS).

But the MP has so far failed to respond to questions from DNS, including what conclusions she has reached about the safety of the PIP system, in the context of the billions of pounds her sister has been trying to cut from PIP spending, and whether she would be taking any action on her constituent’s behalf.

Reeves has also refused to comment on the possible harm that could be caused to other disabled people like Tracie if the billions of pounds of cuts to PIP had gone ahead.

DNS first put the questions to Reeves on 7 April, nearly three months ago.

The ombudsman had concluded that DWP’s failings in dealing with Tracie’s PIP claim were a “significant contributing factor” in her decision to take her own life in March 2020.

Tracie’s mental health had been stable, but she “spiralled into a deep depression” after DWP removed the daily living part of her PIP following a review of her eligibility in July 2019.

The ombudsman concluded that DWP – which eventually admitted that its decision on her claim had been wrong – failed to consider the relevant evidence properly.

The ombudsman is now looking at whether DWP needs to make “wider changes to its service and the way it considers benefit claims”, as part of a broader piece of work which includes an investigation into the death of another disabled claimant.

Asked for an update on this work, a spokesperson for the ombudsman said: “This work involves an ongoing investigation.

By law we investigate in private so we cannot comment further on this.”

DWP eventually decided – after her death – that Tracie should have been entitled to the enhanced daily living rate of PIP.

DWP accepted that Tracie had needed help from another person to get in and out of the bath; couldn’t wash all her body herself; relied on incontinence pads; needed assistance to take her medication; had paranoid thoughts and felt anxious when others were around; rarely left the house; avoided mixing with other people; and experienced significant mental distress and suicidal thoughts.

But despite her significant support needs, the report shows that someone with Tracie’s level of impairment would not have qualified for even the standard rate of the daily living part of PIP if the chancellor’s cuts had been implemented from November 2026.

This is because to qualify for PIP daily living, a new claimant would have needed at least four points in at least one “activity”, and the most Tracie qualified for in any single activity was three points.

The ombudsman’s findings have therefore been posing a political headache for Ellie Reeves, although that eased this week when a chaotic parliamentary debate saw ministers withdraw all cuts to PIP from the universal credit and personal independence payment bill, with future cuts not to be considered until after a ministerial review (see separate stories).

The ombudsman finally sent Reeves a copy of the report on Monday, three days after DNS had asked when the MP had received the report.

A spokesperson for the ombudsman said: “The usual procedure after a parliamentary investigation is closed is that the report would be sent to the referring MP on the same day as the complainant and organisation involved.

In this case, human error meant the report was not sent to the MP.

We have apologised to the complainant and MP for this error.

We will learn from this mistake to prevent it from happening again in the future.”

*The following organisations are among those that could be able to offer support if you have been affected by issues raised in this article:  MindPapyrusRethinkSamaritans, and SOS Silence of Suicide

3 July 2025

 

Disabled people receiving care were ‘ignored by design’ during the pandemic, Covid inquiry hears

Four national disabled people’s organisations (DPOs) have told the Covid inquiry that people who receive care and support were “ignored by design” during the pandemic.

The inquiry heard on Monday that there were more than 43,000 deaths involving COVID-19 in care homes across the UK between March 2020 and July 2022, although there were no figures given for how many disabled people died in their own homes while receiving care services.

The inquiry also heard that, during the first two peaks of the pandemic, before vaccines became widely available, people with learning difficulties were seven to nine times more likely to experience a COVID-19-related death than people without learning difficulties.

And more than a quarter of all deaths from COVID-19 in 2020 were in people with dementia, even though they only made up two per cent of the total adult population.

Disability Rights UK (DR UK), Disability Action Northern Ireland, Disability Wales and Inclusion Scotland have together been granted “core participant status” in module six of the UK Covid-19 Inquiry, which is examining the impact of the pandemic on the adult social care sector across the UK.

Their opening statement for module six was delivered on Monday by barrister Danny Friedman, from Matrix Chambers.  

He told the inquiry that the pandemic saw care settings become life-threatening, while “care services to sustain everyday basic quality of life were withdrawn”.

He highlighted how the Scientific Advisory Group for Emergencies (SAGE), which provides advice to government during emergencies, stated in May 2022 that no UK country was able to “routinely identify who is resident in care homes, who is receiving social care at home, and who works in or visits a care home or a person’s home”.

These data weaknesses meant the “recipients of care, the way they live, and the way that many of them died, was ignored by design”, said Friedman.

The DPOs’ opening statement said that care staff were allowed to move from care setting to care setting, spreading the virus, because those in charge knew the system would “collapse” if staff were forced to work only in one location.

Friedman said: “Care homes would go under. People would be abandoned. It was decided that the lesser of evils was hazardous movement of staff.”

The DPOs also highlighted how the “very first thing” the UK government did in the pandemic was to “legislate to take their rights away” under the Care Act.

But Friedman said that only eight local authorities in England lodged reports to show they were operating under these emergency care laws, even though the evidence showed there were “vastly reduced services across the country”, which meant local authorities must have “embarked on mass violations of the law”.

He said: “Some local authorities reduced their services to basic life and limb protection, social contact services were drastically cut, leaving people with dementia, learning disabilities and learning difficulties and mental ill-health totally isolated for long periods.

The singular benefit of easements was that the law required reasoned, recorded, and open decision-making about withdrawal of services and disclosure of that fact to central government, but across the system, that is the one thing that local authorities near uniformly appear not to have done.

Government then helped to misrepresent the human cost by finding false consolation that only eight reports were made.

Rather than taking steps to enforce the law, the result is one of the singularly worst failures of accountability, and indeed illegality, across the period.”

The DPOs also highlighted that the government had focused on care homes and not domiciliary or supported care settings when it thought about issues such as providing personal protective equipment, testing for the virus, and getting hold of food.

Friedman said: “All these things were afterthoughts, grafted on to government responses far later than for hospitals and residential settings, if at all.”

The inquiry had heard earlier that its module six investigation had gathered more than 200,000 pages of evidence.

The hearings will last five weeks, and about 55 witnesses will give oral evidence.

Nearly 47,000 people have shared their experience of the care sector during the pandemic with the inquiry’s Every Story Matters listening exercise, the inquiry heard.

After the hearing, Georgia Bondy, who is working for DR UK on the inquiry, said: “The government needs to take responsibility for the fact that its lack of planning, consultation and care is part of the reason so many disabled people receiving care died and suffered during the pandemic.”

Rhian Davies, chief executive of Disability Wales, said: “Curtailing disabled people’s rights under the Social Services and Wellbeing (Wales) Act (2014) was one of the earliest decisions taken by Welsh government at the outset of the pandemic and paved the way for Wales experiencing the highest death rate from Covid-19 amongst disabled people in the UK.”

And Nuala Toman, head of accessibility at Disability Action Northern Ireland, said: “The pandemic exposed a brutal truth: disabled people were not only forgotten, they were disregarded through planning and service design failures.

The UK and Northern Ireland’s fragmented and underfunded care system, combined with institutional ableism, led to preventable deaths and trauma.

Unless our governments act now, we are knowingly walking into the next crisis with the same failures.” 

Heather Fisken, chief executive of Inclusion Scotland, said: “If there was ever any emergency planning around these vital services and supports, disabled people were unaware and not involved.

As a consequence, tens of thousands of disabled people lost vital support, often overnight, and were put at increased risk of contracting COVID.

Today, some still don’t have the support they had prior to the pandemic.

Governments need to take this learning forward and work with our organisations to ensure social care support is invested in and systems around it are strengthened and people-led so that this never happens again”.

3 July 2025

 

Disabled activists warn Labour MPs who vote for cuts: ‘The gloves will be off’

Labour MPs were given their final warning by disabled activists at a sweltering rally outside parliament on Monday that, if they vote for cuts to disability benefits, the “gloves will be off”.

Ellen Clifford, one of the key organisers of the rally and award-winning author of The War on Disabled People, warned MPs of the consequences if they voted for the cuts.

She told the #WelfareNotWarfare rally, which took place a day before MPs voted on the cuts in the universal credit and personal independence payment bill (see separate stories): “I know that disabled people will fight to the end.

We are not going to let this through without one hell of a fight. And if it does, we are not going to forgive any Labour MPs who either vote for it or abstain.”

Paula Peters, from Disabled People Against Cuts (DPAC), said any Labour MPs who voted for the cuts would be forced from their seats.

She said: “Let’s tell these MPs: the gloves come off. We turn the anger into action and we’re not going to back off.”

John McArdle, co-founder of the Scottish grassroots group Black Triangle Campaign, warned Scottish Labour MPs – including his own MP, Ian Murray – that disabled people would “wipe the floor” with them at the next general election if they backed the cuts.

Any of these MPs that vote for this bill… if you vote to push us into the most appalling poverty and despair, we will wipe the floor with you at the general election, we will boot you out of Scotland.”

Among the speakers was Joy Dove, who has fought for justice for eight years for her disabled daughter Jodey Whiting.

She took her own life in February 2017 after the Department for Work and Pensions (DWP) wrongly removed her out-of-work disability benefits following five missed chances to save her.

Dove read out part of the ruling given by the coroner at a long-awaited second inquest last month, which concluded that her daughter’s benefits had been “wrongly” withdrawn.

And she warned that other disabled people could die if the cuts went ahead.

She had a message for the department: “DWP, you killed my daughter, and I don’t want it to happen to anybody else.”

Dr Natasha Hirst, disabled activist and former president of the National Union of Journalists, also spoke of the harm the cuts would cause.

She said the bill would take money from disabled people “who are already struggling to survive.

We know this will harm them, we know this bill will kill people.

MPs need to listen to their disabled constituents. Take the money from those who can afford to pay, not those who can’t.

We will not forget how you vote.”

Welfare rights adviser Emma Cotton told the rally of the damage already caused by 15 years of austerity.

She said: “I have seen the damage that austerity has done. I have been a witness to a near-total degradation of the UK social security system.”

Fazilet Hadi, from Disability Rights UK, was among those who mentioned the government’s pledge that it was now going to start co-producing policy with disabled people.

She said: “That is absolute rubbish. If they had wanted to co-produce with disabled people, they should have talked to us a year ago… they should have put these proposals in the green paper… they should have stopped rushing this bill through.”

She said earlier: “It is absolutely shameful what this government is doing to disabled people, and it will be shameful for Labour MPs if they vote with the government.

Successive governments have made us poor, successive governments have put the NHS on its knees, successive governments have taken away social care, successive governments have made us a society where disabled people are becoming sicker and new disabled people are coming on stream because of homelessness, poverty, and lack of food.”

There were regular outbursts of anger among speakers, including from Mac, from Crips Against Cuts, who told the rally: “Tax the wealthy, instead of killing the crips.”

Several disabled speakers – including Clifford – also spoke of their pride in a disability community that continues to fight, despite 15 years of battling against austerity cuts.

The rally was led by DPAC, and supported by the Taking The PIP campaign and Crips Against Cuts, as well as mainstream campaign groups Stop the War Coalition, The People’s Assembly, The Trade Union Coordinating Group, and We Demand Change.

There were several speeches from members of the disabled people’s Taking the PIP anti-cuts campaign, including actors Cherylee Houston, Lisa Hammond and Cerrie Burnell.

Houston said: “How dare they try to reduce our futures, how dare they try to infer that we are of less value, a lesser part of society.

We need to stand up and hold firm. They cannot strip away years of legacy within our community.

I’m here alongside everyone else to say stop this bill, stop it now before more people die.”

Hammond said the concessions made by ministers were “nothing more than political spin.

They are designed to buy off rebellion, not to protect our rights.”

Among others who warned of the consequences of the cuts was Angela Grant, president of the DWP group of the PCS union, who said: “Many of us, including me, depend on PIP to keep us in work.

I would not be able to work if they came after PIP.”

She added: “They do not care, they are not listening, until we make them listen.

We stand together because if we start letting them divide us, divide us in our communities, they will break us down one by one.”

Hamza spoke of the impact on fellow disabled asylum-seekers, and he told the rally: “We are here today to fight for our fundamental human rights.

We fight to win, or we die fighting.”

The rally was temporarily disrupted by protesters from a rival rally who supported the right of Israel to continue its genocide in Palestine and to continue bombing Iran, and supported the son of Iran’s former Shah and want to see regime change in Iran.

They had edged closer and closer to the disabled people’s rally, and several of their supporters appeared intent on antagonising and intimidating disabled activists, with several reports of aggressive disablist abuse.

When disabled activists saw this begin to happen, they linked arms with allies to protect disabled people and their rally and continued to chant “welfare not warfare” until the pro-Israel protesters eventually melted away.

Although police officers had been seen dragging away at least two members of the pro-Israel rally, the Metropolitan police said afterwards that they were not aware of any arrests.

Several of the pro-Israel supporters refused to talk to Disability News Service, but one of them claimed they were opposed to Stop the War Coalition, which was supporting the anti-cuts rally, and he criticised the argument that cutting spending on bombs would allow increased spending on social security.

The disabled people’s rally also included songs from disabled activist and singer-songwriter Sophia Kleanthous, who minutes earlier had been part of the human barrier.

Her songs included a new anti-cuts anthem written for the rally: Cut Us Until We Bleed.

As she introduced the song, she told the rally: “We will not allow people to divide us.

We will not support war, and we will not support these cuts.”

At the end of the song, activists displayed a huge new banner, which said: “You Cut We Bleed.”

A string of MPs spoke at the rally to express their solidarity with disabled people, including Labour’s Ian Lavery, Andy McDonald, Richard Burgon, Lorraine Beavers and Brian Leishman, former Labour leader – and now an Independent MP – Jeremy Corbyn, and fellow Independent MP Adnan Hussain.

Burgon told the rally: “You’re saying, and we support you, that enough is enough.

Let’s be clear: this bill was brought to save money. This bill was brought to do that by making things worse for disabled people in this country.”

And he sent a message to fellow Labour MPs: “Certain votes in parliament define you, certain votes in parliament will be remembered not only for the rest of your political career, but probably for the rest of your life.

It’s about time that my colleagues got an inch of the guts, an inch of the courage of disabled people outside here today, and did the right thing.

Don’t talk to me about agonising over the vote – the people agonising are disabled people across the country who are worried about the future.

Don’t talk to me about agonising on £93,000 a year, do the right thing for God’s sake.”

3 July 2025

 

GB News says it has nothing to apologise for, after guest suggests starving disabled benefit claimants

A British news channel has said it has nothing to apologise for after a right-wing commentator and comedian suggested the best way to cut the number of disabled people claiming benefits was to starve, or even shoot, them.

It is just the latest example of disability hate speech broadcast and published by mainstream media organisations over the last 35 years that have run in parallel with government attempts to cut spending on disability benefits.

GB News presenter Patrick Christys had told viewers that “welfare needs to be cut” – while ignoring the evidence that working-age social security spending is stable as a proportion of GDP* – before claiming that the prime minister was not “doing much” to cut disability benefits.

He then asked his guest Lewis Schaffer how he would “get them off their backside”.

Schaffer replied: “Just starve them, that’s what people have to do, that’s what you’ve got to do to people, you can’t just give people money.”

He then added: “What else can you do? Shoot them? I mean, I’d suggest that, but I think that’s maybe a bit strong.”

Christys then replied: “Yeah, it’s just not allowed these days.”

On his X/Twitter profile, Schaffer describes himself as a “virologist, cardiologist, climatologist, historian”, but elsewhere he is described as a “comedian and broadcaster”.

One of the earliest commentators to pick up Schaffer’s comments was “Maximilien Robespierre”, who described the comments on his YouTube channel as “dangerous rhetoric”.

GB News originally refused to comment, but it eventually produced the following statement for Disability News Service (DNS): “Having reviewed the comment, which is clearly comedic, GB News does not consider there is anything that requires an apology, or further explanation.”

But Dr Natasha Hirst, disabled members’ representative for the National Union of Journalists, told DNS: “It is appalling and unacceptable for an Ofcom-regulated broadcaster to encourage and allow discriminatory and harmful commentary about disabled people.

Suggesting violence towards disabled people is no joke and has real-life consequences by emboldening hate speech and harassment.

We expect Ofcom to do its job as a regulator and investigate the complaints raised with a recognition of the wider context of exclusion and abuse that disabled people experience in their daily lives.”

Disabled campaigner Ben Scott called for GB News to be shut down by the broadcasting regulator Ofcom because of the “astronomically shocking” and “appalling” rhetoric.

He said Schaffer’s comments reminded him of Nazi “useless eater” rhetoric from the 1930s, which eventually led to the targeted killing of hundreds of thousands of disabled people in Germany through the Aktion T4 programme.

After Scott criticised him on X, Schaffer repeated some of his comments, posting: “I’m suggesting ‘starving’ or and then ‘shooting’ the disabled, to lower costs!”

This week, Schaffer’s website appeared to have been taken off-line, but Wikipedia describes him as “an American comedian and broadcaster” who is also a GB News presenter.

The comments come just three months after the Department for Work and Pensions drew horrified comments after publishing figures that showed the total cost to the economy of disabled people who cannot work, which was described as a “chilling” echo of the propaganda of 1930s Germany.

Ofcom confirmed that there had been complaints about Lewis Schaffer’s comments, but because there were less than 50, it was unable to say how many.

An Ofcom spokesperson said: “We are assessing complaints about this programme against our broadcasting rules before deciding whether or not to investigate.”

*Gross domestic product, the size of the country’s economy in a particular year

3 July 2025

 

SEND inspections find services in just one in four areas usually lead to ‘positive’ outcomes for disabled children

Only one in four inspections of local services for disabled children in England last year concluded that they usually lead to “positive experiences and outcomes” for those young people, the education regulator has announced.

The findings from Ofsted showed that 28 inspections of special educational needs and disabilities (SEND) services in local areas were carried out in 2024, but only seven led to a positive report.

Six of the inspections – which do not involve inspections of schools – concluded that there were “widespread and/or systemic failings” in local services which led to “significant concerns”, while the other 15 concluded that there were “inconsistent experiences and outcomes” for children and young people with SEND.

The inspections are carried out jointly by Ofsted and the Care Quality Commission, a process which began in January 2023, with every area supposed to be inspected at least once every five years.

Only about a third of 153 local areas have been inspected so far.

Dr Edmore Masendeke, policy and research lead for The Alliance for Inclusive Education, said the figures were “not surprising” and reflected the continuing segregation and exclusion of disabled children and young people within the education system.

He said: “What ALLFIE sees is a growing investment in segregation and deliberate dismantling of any progress made towards inclusive education.”

He said this was happening in areas such as Newham, in east London, where Sir Stephen Timms, the minister for social security and disability, is MP for part of the constituency.

In January 2024, there were 576,000 children and young people aged up to 25 with an EHC plan, and another 1.2 million pupils receiving SEN support in school. 

The worst-performing area since the inspections began in January 2023 is the East Midlands, where four areas were found to have “widespread/systemic failings” and just one was found to be “typically positive”.

The North West has also performed poorly so far, with four failing areas, three inconsistent, and one positive.

The best was North East, Yorkshire and the Humber, with four positive, five inconsistent and none found to be failing; London is not far behind, with three positive, six inconsistent, and just one failing.

Masendeke said: “For years, ALLFIE has repeatedly warned that disabled children and young people are being harmed by all forms and practices of segregated education, which continue across all areas of learning but does not lead to inclusive education experiences, where all students are taught together in the same classroom and settings alongside their peers.”

He added: “ALLFIE is also deeply concerned that just a third of local areas have been inspected so far.

How many more disabled children and young people are enduring the same poor educational experiences, or worse?”

He said the findings came at a time when there were serious threats to the legal protections provided by education, health and care plans.

And he said there appeared to be a “wider move by government to disrupt inclusive education by reducing disability provision and support, redirecting funding from mainstream settings to expand segregated provisions, including building more units within mainstream schools and increasing the number of segregated schools”.

An Ofsted spokesperson said: “These statistics highlight that the outcomes and experiences of too many children with SEND are not as positive as they should be.

We recognise the SEND system is under significant pressure; however, it is vital that improvements are made so children get the support they need.”

The inspections evaluate arrangements for all children and young people with SEND aged up to 25, including those who have an education, health and care (EHC) plan and those who receive special educational needs (SEN) support.

They examine the education, social care and health services provided to disabled children and young people in the local area, including the structure of the local education system, school attendance figures, school transport, employment data for those who have left education, provision of short breaks, transition into adult social care, and performance data on health services.

As part of the inspections, they visit schools and other settings and services, and gather the views of parents and carers, children and young people. 

CQC had not commented by noon today (Thursday).

The Department for Education had also not commented by noon today.

3 July 2025

Other disability-related stories covered by mainstream media this week

Discharging untested patients from hospitals to care homes during the Covid pandemic was the “least worst decision”, the former health secretary Matt Hancock has told a public inquiry. In his testimony to the UK Covid-19 inquiry, Hancock defended the decision – which was later ruled illegal in a high court judgment – to move hospital patients into care homes during the early weeks of the pandemic to free up space: https://www.theguardian.com/uk-news/2025/jul/02/matt-hancock-covid-inquiry-care-homes-hospital-discharge-policy

3 July 2025

 

News provided by John Pring at www.disabilitynewsservice.com

 

Jul 012025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Stephen Timms, the Minister of State for Social Security and Disability, has now replied to the letter from Disabled People Against Cuts sent three weeks ago.

Our letter raised serious concerns with the quality and fairness of the so-called “consultation” being carried out on disability benefit cuts. We asked for the consultation to be extended, and for urgent action to address the failings.

Stephen Timm’s reply, available here, does not address any of the concerns, and he refuses to extend the consultation process.

The minister has not yet replied to the letter from DPAC Cymru, also sent three weeks ago, requesting a meeting following the failures of the DWP in organising the only in-person consultation on the disability cuts in Wales. That letter said:

We are concerned you still do not understand the failures of your department. We have had no indication from you, or the DWP, whatsoever, in any statement, that you understand that the consultation was organised in a way that was unsuitable for disabled people.

Given Timm’s lack of understanding of his department’s failures, we have no confidence in him leading a wider review into PIP.

Jun 272025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Dear Liz Kendall Secretary of State for Work and Pensions,
(For the attention of all MPs and ministers)

We the undersigned are trade unionists opposed to the Universal Credit and Personal Independence bill, designed to restrict access to PIP and to reduce the sickness element (LCWRA) of UC. We believe this is shameful anti-worker and anti-working class legislation.

We represent union members, advisers, caseworkers, officers, housing workers, work coaches, local government and charity workers, finance sector workers, and other roles who work with those on the sharp edge of the disability benefits system. Some of us are also disabled members or carers across our unions, with the double whammy of working in these organisations and being financially impacted. Over a decade of austerity has forced disabled people into even greater poverty, and these cuts will only exacerbate the underlying barriers and widespread discrimination that still shut disabled people out of the workplace.

Our experiences and knowledge of this sector can provide vital insight into the catastrophic impact the proposed welfare cuts are likely to have. The benefit system is already a punitive, degrading, and impoverishing system that has cost lives through assessments, sanctions, and disallowance of benefits. These cuts will only worsen that reality. Cuts kill – particularly as hundreds of thousands more are pushed into poverty.

Not only will these cuts cause increased financial hardship for some of those made vulnerable by a disabling society, but will also add considerable expenses and a much increased workload to workers in several sectors. This is because more people will be plunged into debt. More people will be served with eviction notices (as they won’t be able to pay their rent/bedroom Tax/service charges). In many cases, disabled workers will be faced with the possibility that they will lose PIP and no longer be able to afford to service the additional needs that enable them to remain in the workforce. Cutting incomes will push people further from work, just as sanctions do. This will create misery and resentment in addition to requiring further public services & resources.

The Disability Policy thinktank forecast that the cuts will lead to £1.2bn in extra costs for the NHS and local care services provided by councils, raising the alarm for both councillors and MPs whether the cuts will backfire even on their own economic terms.

More people:

  • won’t be able to afford food or bills, with 4 million already using foodbanks and limited or cut off energy supplies, whilst those industries’ bosses increase their profits off the back of us all.

  • will have their linked benefits stopped, including carer’s allowance and the carer element of UC, disproportionately impacting unpaid carers, women and children when child poverty and homelessness are already at record levels

  • will be excluded from work or forced into unsuitable work which worsens health, with many working families who rely on UC to top up poor wages also to be hit by the reforms.

Benefit cuts harm all working class people, increasing conditionality and forcing us to tolerate exploitative work and accept poorer terms and conditions. The scapegoating of benefit claimants intensifies division and competition and weakens solidarity in our communities.

Local government departments have faced cut after cut and already struggle to have enough staff or resources to support more in need. The voluntary sector has been needed to act up for several years to plug gaps due to Tory austerity, and currently struggles to meet demand.

Funding for debt advice has been reduced and there is insufficient support to help the current number of people with debt and advice.

Access to Work already sees delays of around a year for decisions to enable disabled people to take equal part in work. This is not being resourced as needed.

The proposed cuts by a Labour government will make all of this considerably worse:

  • It will further strain the already overburdened third and public sector. Staff stress will increase, when many already suffer anxiety and poor well-being in the third and public sector because of understaffing and excessive workloads.

  • Communities will be further demoralised and disenfranchised, or will turn to alternatives that do not represent working class interests.

  • The Trade Union movement should not only fight to defend the social security system from cuts, but also demand a transformative alternative that centres human dignity, regardless of ability to work.

  • DPAC and many others have argued for a welfare system that works for us all, removing the private sector involvement and its punitive measures.

With over £20 billion unclaimed, these cuts and the disproportionate targeting of disabled people do not add up. An FOI request found that 87% of those in receipt of the standard rate of PIP daily living, and nearly half of PIP claimants overall, could stand to lose out under the cuts – the scale is much more significant than the Government is letting on.

CPAG also estimated that the benefit bill has been held down by £36 billion annually as a result of caps, freezes and cuts since the 2010s, including the 2-child limit, bedroom tax and benefit cap. Means-tested benefits have been squeezed for over a decade, plunging people into poverty and worsening their health.

Our welfare spending is relatively low as a share of GDP compared to other European countries, even accounting for the increase in PIP claims, simply reflecting worsening health, increases in retirement age, and record waiting lists. Fraud in the PIP system is negligible. Amnesty have stated the inadequacy of benefits violates human rights, and that the system is consciously cruel – it does not need to be made even more restrictive. Civil society, third sector and disabled people’s organisations have been unanimous in their opposition to these ruthless cuts, with Citizen’s Advice condemning the reforms in a ‘Pathways to Poverty’ report and calling for them to be cancelled.

The proposals on unemployment insurance are a further mockery of this being about ‘making work pay’ – severing the link between national insurance credits someone has earned and their ability to rely on an indefinite sickness benefit if they become unable to work, even when made ill by work itself. The cuts are putting cart before horse: investment in employment support is set to have a minimal impact on getting people into work, with job vacancies falling and the Employment Rights Bill not yet implemented.

The consultation has been focused on a few of the changes, and Wales has not had an accessible consultation. That alone should mean this bill should go no further. The changes are being rushed through Parliament to make savings within rigid fiscal rules rather than improve work prospects, and MPs will not have had the chance to review the consultation responses before voting. At every stage the due democratic process and co-production with disabled people, as the Work and Pensions Committee has also called for, has been sidestepped. This concerns us all as trade unionists striving for a more equitable and democratic society.

Instead of balancing the books on the backs of those who can least afford it, Labour should be making the political choice to tax extreme wealth in society, redressing the runaway inequality that has seen the 50 richest families in Britain own more wealth (over £500bn) than half of the rest of the population. We commend the MPs that have submitted an amendment to Parliament to decline a second reading of the bill, and those who have pledged to vote against the bill. We demand that the Government withdraws these cuts, or the Labour Party will be turning its back on workers and working-class communities across the country.

Signatures: (add yours here)

Luke Dukinfield, Unite, Senior Workplace Rep, NEYH CYNfP RISC & Young Members Committee
Ben Golightly, Prospect member (Tech Workers’ Branch).
Arti Dillon Unite 524 branch CYNfP sector & Southwark Trades Council
Helena Navarrete Plana, Unite the Union
Amelia Bradley-Newby, Unison
Rachel eborall
Clara Paillard, Unite the Union, National Industrial Sector Committee (Not For Profit)
Irene McNally, Unite the Union
Clive Walder, Unite
Dara FitzGerald. Vice-Chair Unite Digital and Tech branch
Eric Segal Kent Retired members (SE100R1) branch committee member
Michael Agboh-Davison, Unite
Sean Brogan Chair Unite Community Plymouth and South Devon
Ben Goldstone, Unite LE1111 Housing Workers branch – Equality Officer and Workplace Rep
Jamie Sims, Unite, former workplace rep
Michael Harrison, Unite The Union, Chair of Unite Community Wales and vice chair of Unite Community National Campaign Forum.
James Clements, PCS
Rob Williams chair Unite LE/1228 branch
Charlotte Powell, Unison and UCU Steward
Joseph Meldau, Equalities Office, Unite the Union, Bristol City Council Branch, & a member of Unite South West Disabled Members Committee
Helen Dunster, Unison Representative
Alistair Tice , Unite Community member
Mike Moore, Birmingham University UNISON, Joint Branch Secretary
David Reid (Treasurer, Cardiff General Unite)
Vicki Morris, UNISON University of Nottingham branch secretary, Higher Education Service Group Executive
Mike Vaughan UNISON Branch Secretary
Catherine mcdonagh
Andrea Gilbert GMB Accompanying Rep
James Brackley, UCU
Ioana Cerasella Chis, University of Birmingham UCU & UNISON branch member
Gurbinder Gill, RMT
Steve Merriman, South Yorkshire Retired Members Branch
Mark Sage, Unite Community member
Sacha Ismail, UNISON, FBU
Jackie Lederer Unite Community Branch Secretary
Sally Heier, UCU, University of Leeds Branch Committee Member
Kevin protheroe
Millie Wild, Unite
Karen Drysdale, Unison
Tanis Belsham-Wray. Secretary of Unite NE/403/15 (Community, Youth and Not4Profit).
Tamsila Tauqir, UWE UNISON, Vice-Chair
Stephanie Tailby UCU South West Retired Members Branch
Sarah Horton, Unison
Christine Thomas, Unison
Rob Prince, UNISON, Branch treasurer
Serenity baskett, Unite the union, union rep, lgbt committee member
Jonathan Golding, Branch Secretary, Unite Community, Cardiff & Area
Deborah Butt ASLEF Branch Secretary and Union Learning Representative
Celine Petitjean, Bristol UCU, Membership secretary
Jamie Strudwick, member of Unite
Pauline Brady, Unison, Equalities Officer
Kevin Daws, Treasurer of Gloucester & District Trades Union Council, Branch Equalities Officer of Gloucester SW/007 Branch, UCU South West Regional Equalities Officer
VC – UCU UWE
Bev Keenan Unite Community branch secretary
Barbara Hulme, Unite Community
Sue Wilbraham, Cumbria UCU, Environment rep
Ajit Chuhan UCU Bristol
George Gray
Leisa Taylor, Unite
Ian Townson, Unite Community, Equalities Officer
Lee Starr-Elliott CWU Bristol and District Amal vice chair, equality officer and SW regional disability officer
Pippa Dowswell, Joint Secretary, Islington NEU
Elane Heffernan, UCU Kent Equalities Officer (and PIP claimant)
Eleanor Lisney, NUJ member.
Elizabeth Mawle, Unite
Gwen Vardigans activist Unite community
Katharine Johnston, UCU
Sandra Wyman Unite Community
Zarria Phillips Bristol & Glos area Unite Community
H.Benjafield
Stephanie Mulrine, UCU North East Regional Committee
Steve Jones. CWU Senior Field Official. Convenor Haringey Community Action Network
Matthew D Smith. UCU Treasurer, University of Cumbria
Mark Evans Retired members secretary Carmarthenshire County Unison and member of Carmarthenshire County Unison branch committee
Penny Foskett, NEU, retired
James Jackson Unite Community
Gemma Southgate, TSSA Executive Committee Member for Wales & Western Division
Mathew John, Branch Chair, Carmarthenshire County Unison Branch
Melissa Heywood, TSSA President
Trevor Jones (Unite the Community)
Kevin Pattison, unite community, chair Leeds, Wakefield & York
Samuel Coxson, Unite
Monique Buchli
Gary Clark CWU retired member former branch secretary
J. Losh, Worcestershire Unison
Andrew Kilmister, UCU, member of Oxford Brookes University UCU Executive
Cllr Alexi Dimond, Sheffield City Council, Unite – Not For Profit
Emma Cotton, Social Security and Tax Officer, Equity
Jeni Hunneyball Unite
Jane Carter NEU
Marco Tesei, UCU vice-chair West London College, UCU NEC UK-elected
Chloe Cheeseman, UNISON member
Martin Cavanagh, PCS National President
Saul Cahill, PCS NEC member
Lucy Burke. UCU vice chair, Manchester Metropolitan University
Jennifer Forbes, UCU branch Chair,
Bee Hughes, secretary LJMU UCU
Deji Olayinka UTAW-CWU Chair
Philip Furnivall, Unite, Bristol City Council Senior Craft Workplace Rep – Local Authorities National Industrial Sector Committee
Roland Rance, Treasurer East London Unite Community
Jade Brown, Unison
Amber Williams Unite, co. Vice secretary Bristol city Council branch
Pat Freeman; University of Cumbria UCU H&S rep
Rachael Tomlinson, Unite Community, Humber
Rada Daniell, East London Unite Community member
Ellen Robottom, Unite, former therapeutic counsellor
Fennelia MacCallum, City of Bristol College, LGBT+ Rep
Lisa Lonsdale (Prospect)
Sue Mew – East London Unite Community
Adi Kuntsman, Manchester Metropolitan University
Andy Mitchell, Unite South West Regional Community Forum chair
John Pearson, Unite Community member, former PIP and WCA support worker
Demaine Boocock, UNISON
Elisa Middleditch Unite
Alex Moore President Plymouth NEU
Jan Egan, GMB and Unite Community
Mark King, GMB
Carole Vincent, TULO East London Unite Community & delegate to Waltham Forest Trades Council
Duncan Davis, CWU, UTAW Branch Secretary
Doreen Mcnally. Unite the union
Jan Pritchard
Julie Connolly UCU
Robbie Woodland President BFAWU kernow (Cornwall)
William Kerr, UCU
Vince Martin, Greater Manchester Unite Community, former Branch Secretary
Eddie Hyndes, Musicians’ Union
Neil Terry NUJ
John Fones, UCU.
Tony Staunton, President, Plymouth Trades Union Council
Dave Robertson Unite Community Leeds Wakefield York
Gerry Lavery, Unite Community, Leeds, Wakefield & York.Branch.
Phil Maxwell, Unite Community (branch equalities officer).
Darren James CWU
Jenny Atkinson, UNISON, UWE International Relations Officer
Steve Wilkins Vice Chair Kent Unite Community Branch Secretary Medway TUC
Ryan Aldred Usdaw Assistant Secretary
Chris Bligh, RMT Trades Council rep
Catherine Hughes. Unite Community
Paul Grunnill Unite NW 567 Branch Secretary
Gareth Boyce Unite Union shop steward
Kate Hunter Unite Community
Duncan Moore, UCU National Executive Committee and Secretary of Torbay and South Devon Trades Council
Ian Hanton, Unite Rep
Lady Lola Oyewusi Unison
Mads Hodgson IWGB Disability Officer, Charity Workers Branch
Adrian Jackson Unison .northern regional disabled members deputy co-chair branch disabled members officer northern regional rep national disabled members committee
Scott machin unite member
Gordon Waring
Megan Archer, IWGB Charity Workers Branch
Andrew MIles, NE/COM/5, Unite the Union Leeds, Wakefield and York Community Branch
Miguel Saona. MMU-UCU. LGBT+ Officer.
Alan Theasby, Unite Community
Brian Lennie
Gail Ward Hands2Mouth Project, Unite Community
Cecile Remy, UCU, IWGB
Minesh Parekh, IWGB member (charity worker), Labour and Co-operative Councillor in Sheffield
Ross Maidment, Unite member
Laura Louise Hullah, Musicians’ Union, UCU
Open University UCU Exec
Liam Sewell, UCU, Nottingham College Branch Chair
David Eatock Unite
Patrick Shǐ Timmer, IWGB
Susan Pashkoff, Unite Community, Easr London, Chair
Cllr Jakob Williamson, Unite Member
Kat Down, Vice Chair of NASUWT Disabled Teachers Advisory Committee
Claire Rose, Unite member
Michelle Rogers
Janine Booth, NEU Disabled Members’ Organising Forum; Neurodivergent Labour
Diana Neslen unite the community
Cllr Stan Bates Wakefield MDC Unite member
Dean Darley, Springfield Allotment Community Klub Chair
Beth Wright – NASUWT
David Lowe , Secretary Wigan Trades Council
Steve Handford NEU. International Solidarity Officer.
Nick Parker, PCS, Department for Business and Trade Group Organiser
Kerry Wilks, Unite Community National Chair
Tina Harvey UCU Chair University of Cumbria
Jenifer Devlin Unite Community
Ros Garrick UCU
Addele Lynas NASUWT Belfast Association Secretary
Eeva Sointu, UCU
Sean Kelly Northumberland NEU Branch Secretary
Jon Woods, Portsmouth City UNISON Branch Chair
Elinor Hewitt, Unison LTHT Treasurer and Comms Officer
Claire Inglis, UCU, vice chair at UoC branch
Scott Inglis UCU Branch vice chair
Molly Holland, Unite
Jennifer Jamieson unison member
“Richard stallard
Unite community
Unite plymouth activist committee plymouth trade Council ”
Luciano Sgarbi, IWGB Game Workers member
Mark Blacklock, National Union of Journalists; University and College Union
Mary Currell, Unite member
Mark Fogg, Unite, Branch Officer
Alan Short Unite Community Sth Wales
Linda Burnip, Unison
David Kirk, UNISON
John Ingleson UNISON Branch Chair
Pauline Bailey Unison
Rachel Mills, UNISON Member
Valerie Jackson Unison Retired
Fran Amery, Equality Officer, University of Bath UCU
George Newth, Bath UCU
Alex Charnley, UCU postgraduate rep, Bath university
James Bonner, Unite Community Berkshire, Oxfordshire & Buckinghamshire Branch Treasurer
Caroline Corbin. Unison Health Branch Chair
Denis Bangura, Unison
Philip Bayes
Mark Toovey Lead union learning, deputyearly shift rep, CWU
Wolfgang Bailey. Workplace Representative and Welfare Officer for UNHAC Branch
Tam Laidler, NEU
Debra Willis, unison rep LTHT NHS
David Moon (UCU, branch caseworker, former Branch President, University of Bath)
Darren Robinson Unite The Union Branch Chair / Convenor
Paula Peters Chair of London and Eastern Unite community Campaign Forum & Chair of Bromley & Croydon Unite Community Branch
B.Mootu Unison Equality Officer H&S Representative
Darren Cogavin – UCU
Naomi Pennington, UCU
Stephen Hackett, Unite Workplace Representative, CYNFP RISC delegate
Jon Farley, Secretary, Unite Community Leeds Wakefield and York branch.
Mike Bird, Unite
Kev Conway Unite community member
Cecily Blyther, UCU, Chair at Petroc, Co-chair on Anti-casualisation Committee, member of Disabled Members’ Committee.
Dr Nicholas Lalvani of Unison
Daniel Edmondson, UCU, York St John UCU Branch Equalities Rep
Andy Richards UNISON
Jay Coward, Equity London South, Branch Committee
Richard Stanforth, Unite Union rep in a charity working to stop domestic poverty
Jemma Russell, Unison
Michael k usdaw
Nicola Jones Unison Steward
Dan Edge, Equity, Deaf and Disabled Members Councillor
Elizabeth Lawrence, UCU Regional Secretary Yorkshire and Humberside
Thomas Rudman, Unite LE127
Retired Members Plus section of Unite the Union Cardiff, Activist. Senedd Member for Scope since last September 2024, and an Independent for Cardiff North Labour Party and Activist within Cardiff Central and Cardiff North.
Cecilia Wee, UCU National Executive Committee, co-Chair Royal College of Art UCU
Steven Baugh, Unite
Lesley Bratty, UCU
Andrea Abbas UCU.
Paul Kershaw, chair, Unite LE1111 housing workers branch
Eve Miller, UNISON George Eliot Hospital Branch, Assistant Branch Secretary
Ellie Judge, UTAW-CWU, Tech Sector Support Co-ordinator
Dave Barter (Joint District Secretary, Rochdale NEU)
Kim Wheeler, IWGB
Michael Suter – Rotherham Unison LG Shop Steward and International Officer
Leon Highmoor-Bayes, UTAW
Kevin Ritchie, Unite, Cllr Bramley & Stanningley Ward Leeds City Council
Felix Ricketts-mason, UTAW-CWU
Derek Fraser Manchester NEU
Steve Skinner, Bradford College UCU, Green Rep
Graham Cooper, ASLEF Bletchley branch trustee
Graham Croucher, Branch Secretary and Union Learning Rep, Bletchley Branch
Morgan Rhys Powell, UCU
Bill Smith, Secretary Alice Arnold Unite Community WM5105
Russell Hickman, Unite Community Branch Chair, Northants TUC Chair
Judy White, chair Bradford branch of Unite Community
George Lloyd-Burman, IWGB (Game Workers) Regional Organising Officer
Sue Ghany Unite member
Natalie Amber chair of Equity Deaf and Disabled members committee
louise alldridge UCU Equality Rep
Steve Preddy Unite Southwest
Brett Sparkes, Disabled People Against Cuts Trade Union Group Founder
Ian Hodson, Bakers, Food and Allied Workers Union National President
Jo Grady, General Secretary – University and College Union
Adrian Lister, Unite
Ken Fish, Unite
Ash Stokoe, UCU
Skye Cormier, Unite the Union.
Leanne Hubbard Unite the Union
Kevin Green Unite member
April Ashley, Southwark UNISON Branch Secretary & Black Members UNISON NEC (personal capacity)
Ian Clements, Unite LE1111 Housing Workers Branch Workplace Rep, LE Disabled Members Committee, Chair Hounslow Trades Council.
Matthew Watkins, UNITE
Ian Woolcomb
Rosina Siddique Unite Member
Liz Thompson Unite Community Leeds, Wakefield,York
Corinna Herr , Community Union , Caiwu Union , GMB UNION
Ailig Garth-Dòmhallach of Unite the Union (West of Scotland Community SC/100C9)
Joseph Jones Unison
Elie Sharp, UCU
Katie Reilly, Unite, VC of National Young Members
Stuart Hellingsworth, Unite
Matt Bridges, Workplace Rep, Branch Equalities Officer, NW DWC Committee Member, RISC (Finance and Legal) Disability Representative
Christina Malley, UCU Member for UWL, Former Chair of LIPA UCU
Shaun Topen-Cooper Primary School Teacher FT and Ley Local Secretary P&K NASUWT
Benjamin Cross, British Veterinary Union in Unite
Sandy Simmons – Unite – Equalities Officer
Mary Mullen UCU
Alison Campbell, UNISON, Steward.
Dave Nellist, Unite the Union and former (expelled) Labour MP
Polina Sparks, NUJ, Disabled Members Council deputy chair, welfare and training officer, Manchester & Salford
Justyna Borkowska-Rozanska, VMD, MRCVS, Unite, Reading
Mark Findlay, Unite
Ajay Kumar Bristol Palestine Alliance chair
Sharon-Theresa Calvert, Caseworker, NASUWT
Harry Stamp – UCU London Representative / Committee Member YSJ
Florence Allaway presedent of Haringey trade council
Neil Moore Unite workplace rep Peterborough
Paul Couchman, branch secretary, Surrey County UNISON
Damian Cosgrove, Chair, Unite Not For Profit SE Region SE/6290
Ruairí Lewis, UNISON Local Government Branch, Senior Steward
Jane Fernandes Unite the Union London
Ben Radley, UCU Rep, University of Bath
PCS ARMS Treasurer SW
Dr. Alex Marshall, UCU Hallam Rep
Steve Wright – General Secretary, Fire Brigades Union
Bob Monks, General Secretary – United Road Transport Union
Caroline Clarke, Unite, Sheffield
Sarah Boden BVU Unite member Liverpool
Harriet Knafler, Prospect, South Yorkshire
Ellie Wood, Unite London & Eastern Disabled Members’ Committee and Vice Chair London & Eastern CYWNFP Regional Industrial Sector Committee
Sam Dennehy, Unite Member
Julen Puertas Baños, IWGB, Bromley
Candice George IWGB
Alan Burgess Chair Portsmouth and District Unite community
Rowena Fehilly PCS ARMS
Dave Vincent PCS ARMS
Cllr Cien Elan Butler, Billericay West – Unison Member
John Sweeney Unison London
D Fearn Unison West Midlands
Cathy Meadows UNITE Nottingham
Chris Jackson
Brian Birtwell PCS Lancashire
Elaine Fullaway, Unite, Secretry, Southampton
Holly Notcutt, unite, Great Yarmouth
Michael Lehane – NEU member, President Coventry & Warks BPTU&AA
Gareth Bromhall, Secretary – Swansea Trades Council, GMB Wales and South West Regional Council, TUC Cymru General Council
Teresa MacKay, Branch Secretary, Unite Retired Members National Committee
Anne Boden Work Place Representative Unite the Union
Lesley Pollock, TSSA, Chair, West of Scotland Branch 850
Jacob Goddard, Unite
Tony O’Hara, Unite Member, London
Declan Clune. Secretary Southampton & South West Hampshire Trades Union Council
Jan Underwood, retired, ex-UCU, secretary Arfon Access, Bangor
Mick Morgan Unite N/W community forum chair Lancashire
Jamie Johnson, member CAIWU
Lesley Jones, PCS, Emp Relations Representative, Devon
Jenifer Devlin Unite Community Leeds, Wakefield and York
Mary, Liverpool Unite Member
Caroline Martin UCU Manchester
Zoey Corker Welfare Officer Leeds UNISON
Ekua Bayunu Unite Community Manchester
IAN LOVEGROVE, UK CITIZEN
Stephanie Spierling ARMS member
Dot Tomkinson Disabled members officer Salford City Unison and Co Chair of the North West disabled members committee.
Nixon Tod, UNISON, ex chair National Further Education Committee, retired member, Manchester
Adam Harmsworth, Napo National Vice-Chair
Marcela Leite, Unison Hackney, Green Rep
Suzanna Hudson-Cooke, Chair, British Veterinary Union in Unite
Pete Keenlyside CWU National Honorary Member, Greater Manchester Branch
Sarah Woolley General Secretary BFAWU
Hannah Fyson, UNISON retired member, Manchester
Douglas Stephen Pearce, Usdaw Branch Chair A216 Weston-super-Mare
Colin Carter, RMT, LDC rep Bristol & Area H&S rep Bristol
Louise Branch UNISON, SW
Nathan Lee Davies, UNITE, Wrexham
Steve Gillan General Secretary POA
Helen Thornton, UNISON Steward, Bristol
Jenny Lennon-Wood, Secretary of Dorset Trades Union Council
Joyce Rutherford, Unite Community member
Dave Murphy, Unite Community Teesside and Durham Branch Chair
Nick Caines, UNISON, Branch Chair, North Somerset
Nicola Kingaby RCN
Michael Braithwaite – Unison Member – Weymouth.
Lee Norman, ASLEF Branch Secretary and H&S representative, Darlington
Trevor Saint, Unite Bournemouth branch
Leigh Hodgson, GMB, Gateshead
Alison Hann, UNISON, Bristol LG
Lady Walker. Retired RAF Squadron Leader. East Midlands
Zeal Machin, BFAWU, Branch 547, West Yorkshire, FTW Representative
David Bird
Richard Holland, Salford City Unison Steward
Secretary of Unite retirement branch. Dorset and Bournemouth.
Jane Haden – Treasurer of Unite Community South Devon Branch
Jane Nellist, President of Coventry TUC and member of NEU
Siobhan Strode, Unite Community, Devon
Paul Hunt, branch chair, Coventry City UNISON and delegate to Coventry TUC
Linda Gates, Unite Community member
Julian Wilson, PCS, MoJ Group EC, Chair, Royal Courts of Justice and First Avenue House Branch.
James Foster, Unite Community, Orpington
Phil Watts – Branch Secretary Unite Northants Retired Members
Andy Hunter-Rossall, BFAWU member
Carole Vallelly GMB member
Stephe Meloy – Musicians’ Union member
Dave Levy – GMB London Regional Council
Michael Torrens, Unite, Equalities and Communications Officer
Mark Colpus, UCU
Dave Ray, CWU, Industrial Relations Rep & Chair NE Political Committee, Nort East
Dave Gorton, Unite LE372 branch publicity officer
Fredy Velez – BFAWU Rep Suma Wholefoods Branch
Stephen Brown, GMB & MU
Anna – FDA, senior policy advisor in Civil Service and enhanced PIP recipent
Jackie Owen Unite Community, Equalities Officer NE Wales
Lucy Fyson GMB member
Alice Tibbs, CAC Portsmouth
Jackie Lederer, Unite Community, Portsmouth and District Branch, S E Region
Kathleen Sowden unite south devon
Christine Wilson Bristol Bath & Gloucester branch Unite Community
Felix Manocha-Seymour, NEU Portsmouth
Lynne Batty, NEU, Leeds
David Kersey – Communications Officer- Coventry City Council
Peter ROBERTS, NEU, Hampshire
Stephen Lennon-Patience Unite Health member Dorset
Ben Willis, USDAW,North Somerset
Catherine Crowther Unite Community Member
Willow Tyers, NEU, Southampton
Heather Juno Libertine Rennie, Prospect
Naomi Byron, UNISON, London
Teresa MacKay, LE/2116 Branch Secretary, NRMC
Sarah Sanford, Branch Equalities Officer Suffolk Unite Community & former Welfare Rights Adviser Ipswich TUC UWC
Rebecca Short: Equity Union Member, Portsmouth UK
Mehreen Begg NEU Executive London
Pete Bloomer, Unite Community, social media officer, Birmingham.
Joy Bazeley, Southsea, Unison
Ben Jackson OT & GMMH UNISON Branch Secretary
Andrew Thompson, Unite, former national convenor CGL, Birmingham
Tim Cutter Unite 524 branch
Bee Tidbury
Nancy Taaffe, Workplace rep,Unite
Alexandra Summerson, National Education Union, Northern Region Disabled Members Organising Forum Rep, NYH TUC Executive
Des Merritt, treasurer, UNISON.
Mélusine Lenoir, London, Equity Member
Pam Wortley – Unite
Bill Smith -Secretary of the Alice Arnold Unite Community Branch Coventry and Warwickshire
Wyn Turner, GMB member
Hayleigh Marks Talabis, FBU East Midlands Regions 6 Control Rep & Political Organiser, Northamptonshire Control Branch Secretary & Northamptonshire Fairness at Work Rep
John Whittall, Unite Retired Members, Northampton Branch.
Chairman: Respect for the Unemployed & Benefit Claimants
Sadia Mirza, Unite the Union, Equalities Representative
Holly Donovan, National Forum rep for the East Midlands, Unite Community
michael jewkes, equalities officer tom mann branch, disability officer North Warks and Bedworth labour clp,
Moe Muhsin Manir – Unite Activist London, Former Representative
Jeff aherne independant
Claire Newland, Suffolk, Unite member – disabled.
David Greenhalf
Sue sanders NEU
Councillor Andy Wilson Unite Community Branch Liverpool
Debby Monkhouse, Unite member
Matt Pinnell West Yorkshire BFAWU member
Joanne Shaftoe, CWU North East Regional Chairperson
Carol Duerden, Unite Community Bradford Branch.
Jean Crocker, Unite Community and UCU retired members, North East England
Cllr Paul R Kimber Labour — Dorset Council.
Ruth Pitman, Dorset
John Shortell, Head of EDI, Musicians’ Union
Charlotte Bjorndal, UNISON – Leeds
Peter Ashmore, Leeds, Unison. (only working due to PIP payments assisting me to get to work. I will lose these and employment if changes go ahead)
Richard Tulloch, Unison, Leeds
Emma Emmerson, Unison, Leeds
“Mark Taylor-Thomas
Unison member, Leeds Branch”
Donna Padget, unison, Leeds
Amy Smith, Leeds
Kathleen Walpole – Unison member – local authority worker and DLA claimant – Leeds
M Kerr, Unison Member, Leeds
Sue Taylor Unison Leeds
Laura Topping, Unison, Leeds
Kimberley White -Unison -Leeds
Eleanor Hastwell, Unison, Leeds
Joseph Babalola,union member,christian,Leeds
Kathryn Russell, Leeds, Unison Member
Angela Stocks Leeds
Uyi Dickson & Yorkshire – Humberside Region
Dwain reid union west yorkshire
Lee Paton, Leeds.
Lee Paton, Unison, Leeds.
Ruth Armitage, Unison member, Leeds Local Government
Shirley Norman UNISON Yorkshire and Humber Leeds
Phil Marsden,West Yorkshie Unison
Jordon newton leeds
Freddie Found, UNISON
Farzana Kauser unison member
Joanne, unison, leeds
Ali Phillips – Unison Member – Leeds
Charlie Lowe
Eugene Okwei. Unison. Leeds. West Yorkshire
Dave Roberts, Leeds Unison
Mr Raafat Musa / West Yorkshire-Leeds
Matthew Hawkins, Unison Rep for Leeds Federated Housing
Charles Aninaquah Boadi,Unison Leeds branch member
Tania Boulongne, Unison, Leeds
Dave Roberts, Leeds Unison
Carol Spivey Unison Member
Mariam Boadi Owusu, Unison Leeds branch member
Richard Thackwray unison
Cheryl Ferris Stewart Unison member
Krystie Harris-Winstanley, Unison, Leeds, Otley
Cristian Robu Unison Leeds
Elizabeth Morrison, UNISON member, Leeds
Claire Ray – Behaviour Support Worker – Unison member
Izabela Zolnowska, Unison, Nursery Assistant, Leeds
Olivia Carlton, UNISON
Aishah I, Rotherham, Unison member
Barry barker leeds
MR MOHAMMED ASIM HARAF
Steven Elbourne , Unison , Leeds
Elaine Francis-Truett, Unison, West Yorkshire
Sari Sohanpaul Unison Member Leeds
Alex Moore Presldent Plymouth NEU
Nick Redding, Unison, Shop Steward, Leeds
Stephen Linnecor, unison , Leeds.
Rachel O’Gorman, Unison, Leeds
Luke Glossop, Unison member, Leeds
Martin Forsyth Unison Manchester
Pauline Bailey Unison Chair retired members Leeds
Kaal Rosser, Unite Community, -, Plymouth
Janek Poklad-Retired Unison member and former Steward
Steve dobie unison Leeds
Theresa Falkingham, Unison, West Yorkshire
Jasper Shaw, UNISON member
Irene Oriakhi Osunde. Unison. Leeds
Lulu Spargo, Unison
Simon Beaumont, Unison member, Leeds
Hanna Ayisi, UNISON, Yorkshire and Humber, Leeds
N Hadi – Unison Leeds
Alison Greenwood – Unison – Steward – Leeds
Stephen parsons Leeds
Ciaran O’Se
John Whetton, Unison Member, Leeds
Lorraine Bull unison Leeds
Andrew Sutcliffe, Unison, steward, Yorkshire and Humber
Mehnaz Ali, NEU, Disabled Members Committee member, Rochdale
Richard Tindall, Unison, Leeds
Andy silverman Leeds unison
Sarah Nattrass, Unison member, Leeds
Ann McKelvey UNISON ULR Leeds
NEU Regional Council Member
Angela Marshall Leeds Unison
John Vasey
Raymond Hill, UNISON, Leeds
Martin Tolley Unite member
Elaine Summerscales Unison
lesley greenfield unison
Ganiyat Mosunmola Salami. Leeds
Stephen Taylor, Woodlesford, Leeds
Natasha Clarke, Leeds
Mercedes Potter Unison Leeds Children Social Care
Keisha King, Leeds
Aliya Vasylenko, Unison, Leeds
Kehinde Adewale, UNISON member, Leeds
Matthew Lishman, Unison, Leeds
Bernadette Bidmead Steward Unison ( FE)
Jennifer Fairley Unison member, West Yorkshire
Tim snell unison still working at 68 from Leeds
Samantha Gill unison
Victoria Thain ex social worker Leeds
Lisa Jowett Leeds Union
Lisa Birdsall, Ls14 2hz
Mark Greig : UNISON : Adult Social Care, Leeds.
Tom Baker, Unison, Leeds City Council
Emily uden, unison,leeds
Michelle green
Jacqueline Clifford, Unite
Morag Cumming, Unison
Cynthia Harding unison
Sarah Wilson, Unite Member
Mick Heath Bradford
Danielle Steel – Unison Member
Lindsey mara, unison, Mental Health Homeless Team, Leeds City Council
Gary Murphy Yorkshire and Humberside Member
Yvonne Elliott Unison. Leeds
Nigel Jones – Shop Steward UNISON LCC.
Steve Withers unison
Lynn Gunnigle Unite Community Member
Jason Knowles = Leeds Unison Steward – Leeds Adult Social Care – Social worker
Richard smith Unison Leeds
Ushirika Quashie. Unison. Leeds

Jun 262025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Disabled MP who quit government over benefit cuts tells DNS: ‘The consequences will be devastating’ 1

Disabled peers plan to ‘amend, amend, amend, amend, amend’ after assisted dying bill reaches Lords 4

Minister finally admits that working-age benefits spending is stable, despite months of ‘spiralling’ claims 5

This bill opens the door to scandal, abuse and injustice, disabled activists say after assisted dying bill vote 7

Timms says cuts must go ahead, despite being reminded of risk that disabled claimants could die 10

Absence of disabled people’s voices from assisted dying bill has been ‘astonishing’, says disabled MP 12

Timms misleads MPs on DWP transparency and cover-ups, as he gives evidence on PIP review 14

Ministers are considering further extension to disability hate crime laws, after pledge on ‘aggravated’ offences 16

Making all self-driving pilot schemes accessible would be ‘counter-productive’ and slow us down, says minister 17

Involve disabled people ‘meaningfully’ from the start when developing digital assistive tech, says report 19

Other disability-related stories covered by mainstream media this week 21

 

Disabled MP who quit government over benefit cuts tells DNS: ‘The consequences will be devastating’

Disabled Labour MP Vicky Foxcroft has described how she was left with “no choice” but to resign as a whip over government plans to cut billions of pounds a year from disability benefits. 

In her first interview since releasing her resignation letter last Thursday, she told Disability News Service (DNS) that the four years she spent as a shadow minister for disabled people had played a significant part in her decision.

And she also made it clear that the backbench rebellion over the cuts is “huge”, with many of the critics MPs who are “normally very loyal” to the government.

That became clear on Tuesday, when fellow Labour MPs – led by 11 select committee chairs – published a “reasoned amendment” which “declines to give a Second Reading” to the bill, although this is unlikely to be selected to be voted on by the speaker.

She has signed the amendment, which is currently supported by 162 MPs, including 126 other backbench Labour MPs.

Foxcroft says she was taken aback by the number of Labour MPs who approached her on Friday to share their concerns about the bill, as she came to the House of Commons chamber for the assisted dying bill debate (see separate stories).

“Many have come to me to share their concerns, to say they agreed with what I had said in my resignation letter,” she says. 

“And some of these were colleagues that you wouldn’t maybe have expected to have expressed concerns. 

“These are not the usual suspects from the left of the party, these are people who are normally very loyal and want to be loyal but know the government needs to change this.

“I mean, I’m the same myself, but I was left with no choice.

“I don’t want to speak out like this but the government needs to listen, so I will use my voice to amplify voices that are being ignored.”

It’s clear from Sunday’s interview that if she had thought she could effect change from within government, she would not have resigned, but she made her decision to quit when the bill was published last Wednesday, and she saw that ministers had made almost no changes since March’s green paper.

The next day, she resigned through a letter to the prime minister.

In fact, as DNS reported last week, the measures in the bill were in one respect even worse than those suggested by Pathways to Work, because of the misleading reference in the green paper to a premium for those in the “severe conditions group”, which the bill shows will only be a premium for new claimants.

This was confirmed by the minister for social security and disability Sir Stephen Timms, when he gave evidence to the Commons work and pensions committee yesterday (Wednesday).

Foxcroft’s criticisms of the bill are fuelled by her own lived experience as a disabled MP, but also by the evidence she gathered from meeting hundreds of disabled people, including many representatives of disabled-led organisations, during her time as shadow minister.

“We all know the benefit system desperately needs reform,” she says, “but PIP isn’t and has never been about getting people back to work. 

“PIP is there to help disabled people with everyday needs. It’s an in-work and out-of-work benefit, and it’s wrong to deny support from someone who needs help to wash, dress, or use a toilet.

“The cuts will literally remove this basic dignity.

“I couldn’t vote for cuts that would make 800,000 people worse off, with 250,000 pushed into poverty, including 50,000 children. That’s a real human cost. 

“And these cuts don’t make human needs disappear. They just shift the costs onto already over-stretched services such as the NHS, social workers and unpaid carers.

“It’s a false economy, with devastating consequences.”

She says she also understands disabled people’s concerns – evidenced in The Department*, by DNS editor John Pring – about the many deaths of claimants, including an estimated 600 from suicide during the incapacity benefit reforms, when there were similarly significant cuts and reforms to out-of-work disability benefits in the early 2010s under the Conservative-led coalition. 

She is reading the book and is aware that safety and safeguarding must be a key priority with any reforms, because of the risk of unintended consequences.

During Sunday’s interview, she repeatedly stresses the crucial part played in her decision to resign by her four years as shadow minister for disabled people, leading up to last year’s general election.

She says her engagement with disabled people while she was shadow minister showed her just how badly many of them had struggled through 14 years of Conservative government, and she stresses her admiration for those she worked with, even those who “shouted” at her when her party did not go far enough on disability policy.

“They were desperate to see the change that a future Labour government would bring for them,” she says.

“I said as shadow minister that we would work with them to ensure that changes that affected them improved their lives, but that has not happened.

“These changes we’ll be voting on have not been consulted on with disabled people and disabled people’s organisations, and it’s so important to make sure that consultation happens and their voices are heard when such big changes are taking place.

“That is one of the reasons I resigned.”

She made the same point in Friday’s debate on the assisted dying bill – which she voted against – when she spoke of the “negligible” consultation there had been with disabled people about the legislation, and told MPs: “Disabled people’s voices matter in this debate, and yet as I have watched the bill progress, the absence of disabled people’s voices has been astonishing.”

She is hoping ministers will receive this subtle message: that government must engage with disabled people right from the start of any policy-making process that will affect them.

Despite several questions from DNS, she refuses to criticise work and pensions ministers, including Liz Kendall.

But asked for her message to the prime minister, she is blunt. “He needs to revisit it,” she says.

Despite that bluntness, and her high-profile decision to quit as a whip, her resignation letter makes clear that she is fiercely loyal to the government, but just intensely frustrated at the deeply harmful proposed cuts to the universal credit health element, and particularly to PIP.

She points to government policies that would allow people on out-of-work disability benefits to try work without fear of having to go through the assessment process again if it doesn’t work out; reform Access to Work; introduce disability pay gap reporting; and ensure all disabled claimants have access to a supportive work coach if they need one.

But she says: “We need to be doing those things first before we even start considering how we are going to be reforming disability benefits. 

“And when we do eventually do that, we need to make sure that we do it with disabled people and organisations run by disabled people.”

She also lays a large part of the blame at the door of the Department for Work and Pensions (DWP) itself.

She knows from her time as shadow minister that many disabled people have zero trust in the department.

“This bill is most definitely not the right way to persuade disabled people to trust DWP,” she says, “and certainly not when we’ve not worked with them to ensure that we get this right.”

Speaking on Sunday morning, three days after her resignation letter was published, she says she is finally finding time to think after the “whirlwind” media storm it caused, but she insists she has no feelings of regret, although she is sad she had to take the step she did.

“I’m sad to leave my colleagues in the whips office, who I think are absolutely brilliant and do really good work,” she says. 

But there is also a keen sense that she knows time is running out to persuade the government to back off, with the bill’s second reading set to take place on 1 July.

“I want to see the government change this. Desperately. 

“They need to listen to what I’m saying, to what Labour MPs are saying, and what disabled people are saying.”

26 June 2025

 

Disabled peers plan to ‘amend, amend, amend, amend, amend’ after assisted dying bill reaches Lords

The disabled peer who has led UK opposition to the legalisation of assisted dying for decades has pledged to work to make a bill passed by MPs so “tight” that only a very few people will be able to take advantage of it.

Baroness [Jane] Campbell said she believed that if the legislation made it easy for people to take advantage of the new laws – if they are eventually approved by parliament – then “people for whom this bill was never intended will die in their droves”.

She was speaking to Disability News Service (DNS) just minutes after MPs had voted by 314 votes to 291 on Friday afternoon to approve the terminally ill adults (end of life) bill, which will legalise assisted suicide in England and Wales for some people diagnosed with a terminal illness, in certain circumstances.

The crossbench peer, who herself has a progressive condition, said she believes her task as a member of the House of Lords – which will now examine the bill in detail – will be to “amend, amend, amend, amend, amend, so it becomes so tight that anyone would find it difficult to get it”.

She also said her task will be to ensure there is no “slippery slope” that will allow the bill to be extended to an ever wider group of people.

But she said that even if she and fellow peers were successful in amending the bill to make it safer, they were “not miracle workers”.

Baroness Campbell, founder of Not Dead Yet UK (NDY UK), which sees legalisation of assisted suicide and euthanasia as “deadly forms of disability discrimination”, said: “There will be mistakes and people will die, whom if they’d had the right support could have lived a good life until they died, but what else can we do?”

She added: “Why choose people like us to help to die when they can so easily put in support and care to help people live dignified lives at home so that they can cope with the bad times, and get through them.

“Because people do get through them and it is possible to have a good death with a progressive or terminal illness. This is what people forget.”

Her fellow disabled crossbench peer, Baroness [Tanni] Grey-Thompson, who has also spent years opposing legalisation, supports Baroness Campbell’s strategy.

She said: “There are very few safeguards in [the bill] currently. Very few amendments were voted on.”

And she said there was no protection in the bill for people with Down’s syndrome or others with learning difficulties.

Before the vote, Baroness Grey-Thompson told DNS that there would be many amendments proposed in the House of Lords, if the bill was passed by the Commons.

She said: “There’s so little safety in this bill, and so little understanding of the lives of disabled people, and the current government’s plans for welfare.”

Last week, NDY UK released polling showing that two-thirds (65 per cent) of disabled people believe that if benefits are being cut – as they are currently through the Labour government’s universal credit and personal independence payment bill – disabled people living in poverty may be likely to seek an assisted suicide instead of struggling financially.

26 June 2025

 

Minister finally admits that working-age benefits spending is stable, despite months of ‘spiralling’ claims

A minister has finally admitted that spending on working-age benefits is stable, and is not spiralling out of control, despite months of claims from his own department and fellow ministers.

Sir Stephen Timms made the admission as he told the Commons work and pensions committee that ministers had decided not to carry out a public consultation on the billions of pounds of cuts to personal independence payment (PIP) and the disability element of universal credit because of the “urgency of the changes needing to be made”.

He was giving evidence in the committee’s final session of its inquiry into the government’s Pathways to Work green paper.

Sir Stephen, minister for social security and disability, said that spending on PIP had risen in real terms from £12 billion in the year before the pandemic to £22 billion last year, which he said was “not a sustainable trajectory”.

But the committee’s chair, Labour MP Debbie Abrahams, asked if he accepted the evidence of Ben Geiger, professor of social science and health at King’s College London, who had told the inquiry that working-age social security spending had remained at about five per cent of GDP* for the last decade.

Abrahams also asked Sir Stephen if he accepted that the rise in the number of PIP recipients has been due to demographic change, the nation’s poor health, and the increase in the state pension age.

The minister replied: “Well, yeah, I mean, much of what you say, I completely accept.”

He added: “I think that working-age social security spending as a percentage of GDP isn’t much more now than it was before the 2008-2010 recession, but as you say, the share on disability and incapacity benefits is very substantially up.”

He said most of this increase was in the last six years, and that while the “incidence of disability” had risen by about 17 per cent since just before the pandemic, the incidence of “benefit claiming” had risen by 34 per cent. 

Abrahams suggested an explanation for this was that more disabled people were needing to claim PIP because of financial pressures.

Sir Stephen agreed, and suggested that the government needed to cut spending on PIP, even though disabled people were only claiming it because they were struggling due to the cost-of-living crisis.

He said: “I think you’re absolutely right. I’m sure that the cost-of-living challenges are a very big factor in what’s happened.

“The people who may well have always been eligible but have not in the past claimed benefit are now doing, and that’s what’s driven this very substantial increase.

“As I say, the current trajectory is not a sustainable one and it is not in the interest of people who depend on PIP for it to be on a financially unsustainable trajectory.”

Disability News Service reported in February that claims by ministers, opposition politicians and the media that social security spending was “spiralling out of control” were false and “ideological”.

Last August, chancellor Rachel Reeves said the previous government had “let welfare costs spiral out of control”.

In January, the Department for Work and Pensions (DWP) said in a press release on benefit fraud that it wanted to “tackle the spiralling welfare bill”.

And in February, in a press release on disability employment, DWP claimed again that benefits spending was “spiralling”.

*Gross domestic product, the size of the country’s economy in a particular year

26 June 2025

 

This bill opens the door to scandal, abuse and injustice, disabled activists say after assisted dying bill vote

Disabled people’s lives will be increasingly in danger because of MPs’ failure to understand the risks posed by the assisted dying bill, devastated activists warned on Friday after the legislation was approved by the House of Commons.

Disabled activists had started gathering outside parliament at 6.30am last Friday in preparation for a crucial debate on the terminally ill adults (end of life) bill before a vote that determined whether it passed to the Lords.

The bill was eventually passed by the Commons by 314 votes to 291 on Friday afternoon, although disabled MPs strongly opposed the legislation (see separate story).

Before the vote, supporters of Disabled People Against Cuts (DPAC) and Not Dead Yet UK (NDY UK) held up traffic in front of the House of Commons with a last-minute direct action, accompanied by chants of “we are not… dead yet”. 

Author and activist Ellen Clifford, who has helped lead disabled people’s opposition to the bill over the last year, said she trusted the Lords to improve the bill more than MPs, some of whom she said had acted on “naked ambition” and the principle of assisted dying, rather than what was in the bill.

She said she hoped the bill’s passage through the Lords would improve the safeguards and provide opportunities “to show what a shambles the bill is”.

Among those disabled people outside the Commons was musician and activist John Kelly, who said after the vote was announced: “The truth is, our voices haven’t been listened to. 

“What this does is open the door for injustice. 

“To rely on a panel to decide my life of social workers, and psychiatrists, have you not read how many injustices and mistakes those people have made, how much abuse and how many rights have been denied disabled people?

“And what they have done is open the door to allow in yet more scandals, yet more abuse.”

Disabled activist Anna Landre told Disability News Service (DNS): “A lot of us are scared about the prospect of enshrining a state-funded ability to die when we don’t have properly-funded state services to live with dignity, let alone to thrive, let alone to get disabled people into work, like this government claims it wants to do.”

She said: “I most certainly don’t feel safer now.

“I think it’s going to create an atmosphere for disabled people that is increasingly unsafe, when our services are being stripped from us, when we’re going to have to fight even harder to get the basics, the scraps that we can already barely access and now in any medical, in any doctor’s office we enter, we face the prospect of being offered a death, of being offered [an assisted suicide].”

She said it was particularly unsafe for disabled people who face multiple marginalisations, including disabled women, who are more likely to be in an abusive relationship; disabled people of colour, who are more likely to be doubted by their medical practitioners; and disabled people of low socio-economic status, “who are looking at not being able to pay rent next month”. 

She added: “As a disabled woman, I’ve been trying to access a cervical cancer screening for over two years. 

“I wish this government would work on that rather than working on streamlining my access to suicide.”

Another leading activist, Simone Aspis, said that, as a disabled woman with learning difficulties, it was “a very sad day for our community”.

She said the bill was “really, really dangerous”.

She said she believed that, for her and other people with learning difficulties, assisted dying will become the “de facto” treatment option given to them by doctors.

She said: “The government keep saying that there is not enough money to go around, so we are going to spend money on creating an assisted dying service? 

“Where is this money going to be found? It’s going to be taken away from education, from care, from housing, from anything that supports us to have good lives.”

Aspis also pointed out that people with learning difficulties had been “excluded from this debate” because the bill had not been made available in easy read. 

Dermot Devlin, co-founder of DPAC Northern Ireland, said that, with the government’s cuts to disability benefits coming in, it was “a dangerous country now if you’re disabled… but we will keep fighting back.”

Chelsea Roff, a researcher and founder of the US-based charity Eat Breathe Thrive, who has fought for months to alert MPs to the risks the bill poses to people with eating disorders, said: “I’ve spent the last six months trying to raise awareness about this loophole, and hundreds of experts have warned parliament: charities, people with eating disorders, physicians, doctors, lawyers…

“I did that because I thought it was the right thing to do because I thought if MPs understood the evidence, they would act on it and amend the bill.

“I’m really disappointed and I think the evidence was minimised, it was dismissed, it was not meaningfully engaged with.”

Michael Lorimer, from DPAC Northern Ireland, said he was concerned that the bill gave ministers “massive executive powers”.

He said: “Given what they’re doing on benefit cuts, we can’t trust them to represent our best interests in terms of implementing this legislation. 

“It’s getting to the stage where Labour are a clear and present danger to disabled people’s lives here because of the benefit cuts and because this bill has gone through, giving them almost unlimited powers in terms of how they shape this legislation. 

“And they’ve been clear through the benefit cuts that they don’t value our lives.”

Jason de Souza said he believed the new law would be “a catalyst for a much wider agenda against disabled and vulnerable people, especially people who are in a situation where they need palliative care and support”.

Earlier, disabled activists had gathered nearby to share their final thoughts before the vote, after months of campaigning.

Devlin had told fellow protesters: “As a disabled person, this assisted dying bill breaks my heart. It terrifies me. 

“It tells me that my life, already pushed to the margins, already made harder by endless cuts and cruelty is… now disposable, it [turns] the language of choice and dignity into something darker.

“I want to live, I deserve to live, but this bill makes it clear to them that lives like mine are just too expensive to bother saving.”

The disabled crossbench peer Baroness [Tanni] Grey-Thompson fought back tears as she thanked disabled activists for attending the protest “despite the discrimination they face in their daily lives and inaccessible public transport”.

She said there was “so little safety in this bill, and so little understanding of the lives of disabled people, and the current government’s plans for welfare”.

Kevin Caulfield, former chair of Hammersmith and Fulham Coalition Against Cuts, said: “The bill, and what is happening with the universal credit and personal independence payment bill, really indicates disabled people’s position in society, because we have been sidelined all the way through this process. 

“People with life-limiting illnesses are disabled people and that’s in practice and in law and yet they have successfully managed to portray this bill as having very little to do with disabled people, and that’s a f*****g disgrace and it’s disgusting and the same is happening with the benefit cuts.”

Caulfield was given a terminal diagnosis 28 years ago, and says he “might well have decided to take the option” of an assisted death if it was available then “because I was a newly disabled person, I didn’t have access to other disabled people, I had no access to mental health support, and it may well have seemed like a reasonable option”.

But he said he was “still here 28 years later”, and there were “going to be many people in a similar situation to me, tens of thousands of people that will end up being dead as a by-product of this legislation”.

Disabled actor, writer and activist Liz Carr, said the number of disabled activists who had attended the protest was “amazing” in the context of spending cuts and “the struggle to survive”.

She told fellow activists: “You make me know that we’re right and that even if this goes through today and goes through to the Lords, we just keep going there because we know where this goes, we know what it means, we know how it will impact our community and other communities.”

Paula Peters, who had been the first to start the protest, at 6.30am outside parliament, said: “Whatever the outcome, we keep going, and we keep fighting, and we keep resisting… and we are not dead yet.”

Jamie McCormack, another disabled activist who refused to accept defeat, said: “We will fight on, we will fight for assistance to live, not to die. 

“We will fight to our very last dying breath.”

And George Fielding told fellow activists: “Our most precious public services, and the things on which we all rely, rely on doing no harm. 

“This bill will do harm; its very premise is to kill people, it’s a pre-designed process. 

“We are on the right side of history, always have been, and the resistance starts as soon as we hear the result today.”

26 June 2025

 

Timms says cuts must go ahead, despite being reminded of risk that disabled claimants could die

The minister for social security and disability has insisted that billions of pounds a year of cuts to disability benefits must go ahead, despite the risk that they will once again cause countless deaths of disabled claimants.

Sir Stephen Timms was giving evidence yesterday (Wednesday) to the Commons work and pensions committee about plans to cut billions of pounds a year from spending on personal independence payment (PIP) and the disability element of universal credit.

He was giving evidence to the committee’s final session of its inquiry into the government’s Pathways to Work green paper.

The first question he was asked, by committee chair Debbie Abrahams, was about the health impact of the cuts on disabled people, and whether the planned new employment support and jobs would be available by the time the government begins to implement the cuts next year.

She highlighted how research in 2015 by academics at Liverpool and Oxford universities showed the reassessment of disabled people on incapacity benefit through the work capability assessment was linked to about 600 suicides between 2010 and 2013.

Unpublished research also showed how cuts in 2017 – of nearly £30 a week to payments to new claimants of employment and support allowance who were placed in the work-related activity group (WRAG) – were associated with 130,000 “new onset mental health conditions”, she said.

Conservative ministers were ridiculed when they first announced the 2017 cuts and argued that they would “incentivise” those in the WRAG to find work.

Abrahams had already asked Sir Stephen what estimates the government had made of the impact the bill would have on health, in the light of these two pieces of research, at work and pensions questions on Monday.

He said on Monday that the Department for Work and Pensions was “working very closely with the Department of Health and Social Care to ensure that the health and care needs of people who lose benefits as a result of this process are met”.

And when asked again yesterday about the risk of harm caused by the bill, Sir Stephen said the government needed to make sure that both “employment support” and “health and care support” were in place when the cuts were implemented.

He said that new investment in infrastructure and jobs would be “coming into place” in the next few years, and with “what we are proposing on all of those fronts that we will be seeing the progress that we need”.

He added: “I don’t think it would be a viable option to say, well, we’re kind of not going to do anything about the health and disability benefits for a few years and see how things go.” 

The minister was also asked by Liberal Democrat MP John Milne about government plans to halve the health element for new claimants of universal credit next year from £97 per week in 2024-25 to £50 per week in 2026-27, and to freeze it at £97 for existing claimants from 2026-27.

Sir Stephen claimed there was a “very big incentive” for disabled people to “seek to be classified” as having limited capability for work and work-related activity (LCWRA), and so eligible for the health element top-up.

He said: “If they are classified as LCWRA they get a premium which is worth more than the universal credit standard allowance, and that is unavoidably a massive magnet for people.”

He pointed to a letter he had seen in which an MP’s disabled constituent had said that being classified as LCWRA – rather than as having limited capability for work – would mean they would be paid £400 a month more, which would mean they would be “comfortable”.

But Sir Stephen Timms appeared to suggest that a disabled person being financially “comfortable” on benefits was a bad thing.

He said: “And I think this is a really serious flaw in the current system, that it presents this sort of LCWRA status as a sort of something to aim for, that ‘if only I could get to that, I would be comfortable’, when the system should not be doing that to people.

“That is a very bad feature of the current system. 

“What the system should be doing is encouraging people to aspire to work and providing the support to make work possible and feasible, and so, yeah, we are wanting to substantially reduce that incentive.”

He said this would partly be done by raising the standard allowance of universal credit by £5 a week, as well as reducing the health element.

But Milne suggested that the government was concentrating on “Treasury first, needs second”, when what it should be doing was focusing on “needs first, Treasury second”.

26 June 2025

 

Absence of disabled people’s voices from assisted dying bill has been ‘astonishing’, says disabled MP

Disabled MPs have voted overwhelmingly against the assisted dying bill, and warned that it poses a clear danger to disabled people if it eventually becomes law.

Although the terminally ill adults (end of life) bill was passed by the Commons by 314 votes to 291 on Friday afternoon, disabled MPs strongly opposed the bill.

By Disability News Service (DNS) calculations, those MPs who have publicly self-described as disabled people voted against the bill by seven to one.

Disabled MPs who voted against the bill were Labour’s Jen Craft, Marsha de Cordova, Vicky Foxcroft, Liam Conlon, Emma Lewell and Marie Rimmer, and Liberal Democrat Steve Darling.

The only disabled MP who voted for the bill was Marie Tidball, who spoke repeatedly in favour of the legislation during its committee stage, and whose support has likely persuaded some wavering MPs of its safety. 

Of the eight disabled MPs, only Craft and Foxcroft spoke in Friday’s debate.

Craft told fellow MPs that their vote would have “real-world consequences”.

She warned that the medical establishment placed a lesser value on disabled people’s lives, and revealed that when told of her daughter’s Down’s syndrome when she was pregnant, “the first thing the midwife said to me after ‘I’m so sorry’ was, ‘I can book you a termination within 48 hours.’”

She said she could not support the bill “because we cannot legislate against discrimination and we cannot legislate out inherent bias”, and the bill did not have “the adequate safeguards in place”.

She said: “We have been told that there are panels that will provide a safeguard and take into account all of someone’s circumstances, and whether they have capacity. 

“However, those panels may in exceptional circumstances – the bill does not set out what those are – opt not to even meet the person whom they are discussing. 

“We know that the panels do not allow for family members and carers and those who know that person – if they have limited capacity, a learning disability or are unable to make certain decisions themselves – to play a role in that process or have any right of appeal.”

Craft said it was not the job of MPs to send a flawed bill to the Lords and then “out into the world, hoping that others will do our job for us and that it will all just come out in the wash”.

She said: “That is a dereliction of our duty as members of parliament. 

“If you have any concerns about this bill, now is the time to vote against it. You must do that. 

“You must not think that someone else will do your job for you. It is our decision.”

Foxcroft, who was speaking a day after resigning as a government whip over her concerns about the government’s disability benefit cuts, said she had previously been in favour of legalisation.

But she said that her four years as shadow minister for disabled people, during which she spoke to hundreds of disabled people and their organisations, showed they were “extremely fearful of assisted dying”.

She pointed to the huge numbers of disabled people who died during the pandemic, and those who had “do not attempt resuscitation” notices placed on their health records without their knowledge, which “made them fear for their lives”.

She said: “It made them fear that the authorities thought that their lives were worth less. It also made them fearful of what would happen if assisted dying was brought forward.”

She said disabled people “need the health and social care system fixing first” and “want us as parliamentarians to assist them to live, not to die”.

She said: “Disabled people’s voices matter in this debate, and yet as I have watched the bill progress, the absence of disabled people’s voices has been astonishing. 

“They have wanted to engage. Indeed, they have been crying out to be included, yet the engagement has been negligible. 

“I believe that only one disabled people’s organisation was given the opportunity to provide [oral] evidence to the committee.”

She also pointed to the failure to provide the bill in accessible formats, including easy read and British Sign Language.

She told MPs: “I will finish by saying that I am not opposed to the principle of assisted dying, but until we have a system that supports the right to life, I cannot support it. 

“Until we ensure that all safeguards are in place, I cannot support it. 

“And until the vast majority of disabled people and their organisations support the legislation that is being brought forward, I cannot support it.”

She added: “We are not voting on principles today. 

“This is real and we have to protect those people who are susceptible to coercion, who already feel like society does not value them, who often feel like a burden to the state, society and their family.”

26 June 2025

 

Timms misleads MPs on DWP transparency and cover-ups, as he gives evidence on PIP review

The social security and disability minister has misled MPs after suggesting he has ushered in a new era of openness and transparency in the Department for Work and Pensions (DWP).

Sir Stephen Timms told members of the work and pensions committee yesterday (Wednesday) that DWP was being “much more open” than under successive Conservative-led governments.

He had been asked by the committee’s chair, Labour MP Debbie Abrahams, about the review of personal independence payment (PIP) that he will shortly be leading. 

He was giving evidence to the committee’s final session of its inquiry into the government’s Pathways to Work green paper, which will see billions of pounds a year cut from disability benefits.

Abrahams highlighted how the department had previously failed to share its own secret reviews into deaths linked to the benefits system with independent experts commissioned by ministers.

Disability News Service had exposed how the department failed to share both peer reviews – now known as internal process reviews (IPRs) – and coroners’ reports with the experts commissioned to review the work capability assessment between 2010 and 2014.

Abrahams asked Sir Stephen to reassure the committee that data on deaths associated with PIP assessments would be available to whoever led the review.

He told the committee: “I’ll be undertaking the review, so yes, the information will be available to me, and actually, you know, we are being – not least thanks to your work, chair – much, much more open about all of this now than was the case in the past.”

He said the department “want people to see what’s going on”. 

He said: “There isn’t any benefit for the department in hiding these things. 

“They were hidden too often in the past. And I think that’s one reason why the trust in the department deteriorated so badly, because people can see that things were being covered up and hidden and it shouldn’t have been happening.

“And I’m determined that it won’t happen in the future.”

But despite his comments, the department is continuing to hide crucial information about deaths linked to the disability benefits system.

This week, Disability News Service (DNS) submitted written evidence to DWP’s safeguarding review to highlight how DWP was still hiding crucial information that would expose its past actions and failings.

Last month, DNS reported how DWP had unlawfully failed to respond to a freedom of information request to see a secret “critical friend” paper from 2021 on the department’s safeguarding failures.

It is also continuing to refuse to release recommendations made by IPRs following deaths linked to universal credit, dating back as far as 2020.

DWP is also appealing a decision made by the information commissioner that the department should release to DNS “a paper detailing the impact of errors on vulnerable customers” that was discussed at the 12 October 2022 meeting of the department’s serious case panel. 

And the department is continuing to refuse to release a transcript of a training session on human rights law given to DWP staff employed on working-age benefits. 

These are just some of the reports being hidden by DWP; there are likely to be countless other reports and data being kept from other disabled campaigners and allies.

Sir Stephen said he hoped the terms of reference for the PIP review would be released before MPs rise for their summer recess on 22 July.

26 June 2025

 

Ministers are considering further extension to disability hate crime laws, after pledge on ‘aggravated’ offences

The government is considering whether to strengthen disability hate crime laws even further, after ministers agreed to make a long-awaited improvement that will mean longer sentences for offenders.

Home Office minister Diana Johnson announced last week that the government would act to extend the law so that standalone “aggravated offences” would 

apply to disability hate crime and hate crime motivated by sexual orientation or transgender identity.

She said the government would add an amendment to the crime and policing bill to make this change when it reached its committee stage in the House of Lords, keeping a pledge made in Labour’s general election manifesto last year.

This would mean an offender could be charged with an offence – such as assault, harassment or criminal damage – that was aggravated by hostility towards a disabled person, and they would then face a tougher sentence if convicted.

At present, aggravated offences only apply to racial and religious hostility, and a disability hate crime can only be addressed by a court during sentencing, where the sentence can be increased if prosecutors can prove the offence was motivated by disability-related hostility.

The move was proposed in an amendment to the crime and policing bill by Labour’s Rachel Taylor, who told fellow MPs last week that the current discrepancy “cannot be right”. 

She said: “We cannot say, as a society, that some forms of hatred are more evil than others.”

The amendment was supported by disabled Labour MP Marie Tidball, who said the “opportunity to legislate to strengthen the law on hate crime offences must be seized”.

Disabled campaigners have been calling for the change for more than a decade.

But one leading campaigner said the government needed to go much further.

The aggravated offences change was recommended by the Law Commission in December 2021, but it also made two other key recommendations to strengthen disability hate crime laws.

It called for existing offences of stirring up hatred, which only apply to race and religion, to be extended to disabled and LGBT+ victims.

And the Law Commission also said an offender should be found guilty of a disability hate crime offence if they had been “motivated” by “hostility or prejudice” towards disabled people, rather than – at present – only by hostility.

Dr David Wilkin, a disabled activist, researcher, author* and support worker for survivors of disability hate crime, welcomed the move to extend aggravated offences.

But he was critical of the continuing refusal – following years of resistance from Conservative governments – to implement the two other Law Commission recommendations.

He said: “Now, with the perfect opportunity to bring disabled people into the 21st century by establishing legislative equality, they are choosing once again to make sure that disabled people are treated differently, with their hopes and needs once again relegated. 

“Hate crime campaigners have looked forward to disabled people being offered the same rights as other protected groups in new legislation. 

“But now, having reached this timely and convenient critical moment, the Labour government are deliberately excluding those with the greatest needs from attaining simple, fair, and much needed equality.”

The Home Office has told Disability News Service that it will be considering these two further recommendations carefully.

A Home Office spokesperson said: “This government has committed to making our streets safer for everyone and nobody should ever be harmed because of who they are.

“Criminals motivated by racial or religious hate already get tougher sentences. 

“Now we are making sure thugs who carry out vile attacks against someone based on their sexual orientation, transgender identity or disability will also spend longer behind bars.”

*Disability Hate Crime: Perspectives for Change, is published by Routledge

26 June 2025

 

Making all self-driving pilot schemes accessible would be ‘counter-productive’ and slow us down, says minister

A transport minister has told peers that it would be “counter-productive” – and take too long – to draw up rules that would ensure all pilot schemes of self-driving taxis are accessible to disabled people.

Labour’s rail minister Lord [Peter] Hendy was responding to concerns from disabled peer Baroness [Sal] Brinton, who had asked whether the government would make sure disabled people could use the self-driving vehicles when the pilots begin in England next spring.

The former president of the Liberal Democrats told Disability News Service (DNS) earlier this month that she was “very, very concerned” that the government was planning to allow companies to launch self-driving taxis and minibuses even if their vehicles were not accessible to disabled people.

She told fellow peers that the launch of driverless vehicles was a “once in an era moment”, and that contracts with providers should ensure that ramps and audio and visual announcements are “designed in right from the start”.

She said: “The government need to ensure that taxis and bus-like taxis will have accessibility designed into them. 

“Otherwise, it will be like everything else for disabled people: reasonable adjustments after the event that are expensive for the manufacturer and never perfect for the user.”

Lord Hendy told her the government would be subject to equality laws in deciding how granting a permit could “improve understanding of how these services should best be designed for and provided to disabled and older passengers”.

And he said permits could enforce certain conditions, while “accessibility considerations” would be set out in guidance.

But he said: “It would be counterproductive to specify detailed requirements in regulation for innovative new services.”

He said it was likely that the first driverless vehicles would be “the same sort of vehicles” already used for taxis and private hire vehicles.

He added: “In the medium term, clearly there will be new designs, and there are already some that are suitable for wheelchairs and people with disabilities. 

“We have to acknowledge that automated vehicles are part of an exciting future, but they have to be implemented safely, and she is right that they have to be implemented to benefit all parts of the community.”

He said he had “great sympathy” with Baroness Brinton “striving to make sure that disability is treated in the mainstream, but if we are going to do this quickly, we have to recognise that the early adoption under this act is likely to be using the same sorts of vehicles as are used now”. 

He said: “What we are looking for in the medium-term future is new designs, which should have the facilities such as audio-visual equipment and facilities for people in wheelchairs that she would expect.”

Lord Hendy said the government needed to “design in – as far as we can – facilities for disabled people among this”, but the government “have to get going with this, because it is such an exciting future”.

But another disabled peer, the Conservative Lord [Kevin] Shinkwin, pointed out that deputy prime minister Angela Rayner had spoken of the importance of getting disabled people into work, and he questioned how “the retro, ad hoc inclusion of disabled people facilitates the realisation of that worthy goal”.

Baroness Brinton told DNS afterwards that Lord Hendy’s response was “very disappointing” and that she would now seek a private meeting with him to discuss her concerns.

Transport for All (TfA), the disabled-led accessible transport charity, said the government’s plans, which could exclude disabled people from the pilot schemes, were “unacceptable”.

Megan Barnett, TfA’s policy and public affairs officer, said: “Equal access to transport allows us to be part of society. 

“If self-driving vehicles are allowed to develop without disabled people, they will only deepen existing inequalities.

“We need a strong national policy to ensure that the design and rollout of this exciting new technology includes disabled people from the start, so our whole community can benefit from driverless vehicles, now and in the future.”

The Department for Transport announced earlier this month that firms would be able to pilot small-scale “taxi- and bus-like” services without being monitored or controlled by a human for the first time next spring, before a potential wider rollout when the Conservative government’s Automated Vehicles Act is implemented in the second half of 2027.

The government believes self-driving vehicles could help reduce deaths and injuries on the roads, add new public transport options in rural areas, and have the potential to improve mobility, accessibility and independence for those who cannot drive, including many disabled and older people.

26 June 2025

 

Involve disabled people ‘meaningfully’ from the start when developing digital assistive tech, says report

There must be “meaningful participation” of disabled people in the initial stages of developing new digital assistive technology, if its potential for supporting their independence is to be realised, according to a new report.

The Royal Society concluded that tech companies, researchers and governments should do more to remove barriers and engage disabled people in the design of digital assistive tools and services.

Among the recommendations made by the Digital Technology report*, launched this week, is that governments should not consider smartphones as any less a form of assistive technology than hearing aids, manual wheelchairs, or white canes.

But it also warns that many disabled people globally experience lower levels of income compared with non-disabled people, so digital assistive technology needs to be affordable if it is to be useful.

It calls on governments, technology companies and research funders to explore ways to ensure affordability.

As part of the research, the Royal Society – the UK’s national academy of sciences – commissioned the Research Institute for Disabled Consumers to survey a panel of 850 disabled people.

Three-fifths (62 per cent) of them said they used digital assistive technology, with more than half of this group doing so throughout the day.

The survey found that more than half of users of digital assistive technology (53 per cent) said they could not live the way they did without it.

The report defines digital assistive technology as “any technology that processes information to help make people’s lives easier”, such as audio-to-text apps, wayfinding and navigation apps, wearable health devices, smart home devices, sight assistance apps, and screen-reading software.

The report also calls for statistics bodies to collect more data on the daily barriers many disabled people experience with their sight, mobility, and memory, rather than solely focusing on their self-reported disability identity. 

Sir Bernard Silverman, emeritus professor of statistics at the University of Oxford and chair of the report’s steering committee, said: “As a statistician, I would particularly stress that the data we record, and how we categorise it, affects everything and everyone.

“Data on the functional challenges experienced by disabled people would help researchers and providers to ensure that digital products and services, especially in the AI age, are genuinely responsive to their needs.”

The report was developed by a committee of international researchers and technology experts, several of whom are themselves disabled.

Dr Hamied Haroon, a research fellow at the University of Manchester and a member of the Royal Society’s diversity and inclusion committee’s disabled scientists subgroup, said: “We shouldn’t be developing assistive technologies or policies without disabled people being front and centre of the process.

“How do you capture the day-to-day challenges faced by disabled people, or ensure you’re offering solutions that actually work, unless you talk to disabled people?”

Dr Haroon, a member of the report’s steering committee, added: “These assistive technologies are fundamental to the workplace and our daily tasks – but they can be prohibitively expensive or unusable in some settings.

“We need to look at removing these barriers, whether that’s costs, additional training, or infrastructure improvements – like addressing patchy mobile data services that can cut off disabled people in rural and deprived areas.”

*Disability Technology: How data and digital assistive technologies can support independent, fulfilled lives

26 June 2025

Other disability-related stories covered by mainstream media this week

Nearly 100,000 adults have been denied government-funded social care because of a decade’s worth of spending cuts, a Guardian analysis has revealed. The figures highlight how a range of government cuts have put so much pressure on the English social care service that it is leaving tens of thousands of people without the access to long-term care that they would have received 15 years ago: https://www.theguardian.com/society/2025/jun/25/adults-england-denied-state-social-care-due-to-cuts 

Heathrow “needs improvement” in how it assists disabled passengers, a regulator has found. The Civil Aviation Authority, which conducted the assessment, also gave the same rating to Edinburgh and Glasgow Prestwick airports. It said the three airports have “clearly more to do” in their provision of additional support. Fourteen UK airports were rated as “good” and 11 as “very good”. None were rated “poor”: https://www.independent.co.uk/news/uk/home-news/heathrow-civil-aviation-authority-frank-gardner-edinburgh-terminal-b2776464.html 

The mayor of London has said the government must think again about its plans to cut benefits for disabled people. Sir Sadiq Khan said the proposed changes would “destroy” the financial safety net of many disabled and disadvantaged Londoners: https://www.bbc.co.uk/news/articles/cn9y3q7eergo 

Downing Street’s disability cuts will have a “devastating” impact on women’s health and dignity and could breach equality laws, the government has been warned: https://www.theguardian.com/world/2025/jun/24/labours-benefit-cuts-may-discriminate-against-disabled-women-say-charities 

26 June 2025

 

News provided by John Pring at www.disabilitynewsservice.com

Jun 222025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
A graphic of the DPAC Cymru logo.

There is the main DPAC logo to the left, which is a red, pink, blue, and green circle being held by four hands of different skin tones, with the words "disabled people against cuts" surrounding it, and an upside-down black traingle in the middle bearing the letters D P A C.

On the right is the word Cymru (pronounced cum ree) (C Y M R U) in large letters, and the background of the letters are cutouts of the Welsh flag. Above Cymru (pronounced cum ree) is written the words Disabled People Against Cuts. Below Cymru (pronounced cum ree) are the words Rights, not charity, and the equivilant phrase translated into the Welsh language.

The first vote in parliament is 1st July. Here’s a helpful guide to some things people in Wales can do NOW to help defeat the welfare cuts bill.

These actions are specifically customised for people in Wales, and includes lobbying the Welsh government. However, people not living in Wales might still find the resources useful with small adaptations.

Print out a window poster

Stick it in your window, or on workplace or community noticeboards.

Ready-made

Make your own!

Send yours in!

Contributions welcome! Please send it in to swaneadpac@gmail.com and/or dpaccardiffandvalleys@gmail.com

 

  1. Write to ALL of your elected representatives.

Follow each link for instructions and template letters.

 

  1. Write to the press

 

  1. Get involved!

Here are some ideas (there are many more ways to get involved in addition to those listed here):

  • Share this resource!

    • Bit.Ly/DPAC-Cymru-Defeat-The-Bill
  • Research joining a political party that aligns with your views.

 

Jun 122025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Save the date. Protest the disability cuts.

The government is expected to introduce the disability cuts bill on the 18th of June, and vote on it as soon as July 1st.

They are not even waiting for the sham “consultation” to end on 30th of June.

Disabled People Against Cuts and allies are organising a mass Protest of Parliament on June 30th and a national day of action on July 1st when the second reading of the bill will occur.

More details to follow but it is essential that as many people as possible attend these events.

Some funding is available for travel and other essential costs. Email mail@dpac.uk.net

If you are able to arrange a local protest on July 1st please send us details of your event.

A drawing of the politician Rachel Reeves in a robber's outfit and a sack that says Disability Benefits

Welfare Not Warfare

End Labour’s War on Disabled People

Tax the Rich, Not Crips.

The Government are lying about cuts.

  • Total planned disability benefit cuts are at least £9 billion and not the £4.8 billion being reported.

  • Number of households to be plunged into poverty by the PIP cuts alone is at least 350,000 – 4000,000 including 50,000 children.

  • 1.5 million Deaf and Disabled people will be badly impacted by the changes to PIP, not just the 800,000 being reported.

  • MPs will be forced to vote on the cuts without having all the information and based on the misleading figures that have been reported.

 

Image of a person at the top of a cliff pushing someone out of a wheelchair. The Labour party logo. The Department for Work and Pensions logo.

What can I do as a disabled person?

  • If you’re not already a member – join DPAC!

  • Set up a DPAC group in your area if one doesn’t exist!

  • Participate in DPAC Actions to Scrap the Benefit Cuts

  • Organise locally with other Disabled People to mobilise support for our campaign

  • Contact unions, trades councils, Labour party branches, and build a broad based movement to reverse these austerity cuts.

For more details of local groups and actions, keep checking this page!

 

 

Jun 102025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
Portrait of Stephen Timms MP
Disabled People Against Cuts (DPAC) has today written to Stephen Timms, the Minister of State for Social Security and Disability, to raise our serious concerns with the quality and fairness of the so-called “consultation” being carried out on disability benefit cuts.
We are asking for the consultation to be extended, and for urgent action to address the failings.
We urge the government start again on welfare reform, listening to disabled people and carers in a genuine process of co-production.
This is what we said in our letter:
Dear Stephen Timms,

I am writing to you on behalf of Disabled People Against Cuts (DPAC) to urgently raise concerns regarding the accessibility of the consultation on the benefits cuts proposed in the March 2025 Green Paper. In light of the limited time available for the consultation which is due to close on 30 June 2025, you are asked to take urgent action to address our concerns, confirm what steps are being taken and to extend the time available for disabled people to engage with the consultation given the accessibility issues they have faced to date. In order for the consultation to fulfil its purpose. Disabled people who are likely to be affected by proposed benefits changes, must have a proper and meaningful opportunity to engage with the consultation and accessible arrangements must therefore be urgently made to facilitate their proper participation in the consultation.

Our concerns

The face-to-face consultation in Cardiff on the 3rd June was cancelled less than two days after the venue was announced, with only one working day left before the event.

The DWP has claimed that the Cardiff venue cancelled the meeting at the last minute yet the venue itself was already inaccessible to disabled people. No transport to the venue was offered by the DWP for those who wanted to take part.

The booked venue was only revealed at the last minute. This was despite disabled people asking multiple times, over weeks, for information so that they could plan journeys, accommodation, and access requirements. The venue was far out of the centre of Cardiff, and completely inaccessible for many disabled people, especially at such short notice. It would have meant a wheelchair user travelling 1.6 miles unassisted. Shockingly this was the only face-to-face consultation event for the whole of Wales.

People at other DWP consultations in England have had similarly poor experiences. For example, lack of accessibility of the venue led to only 9 out of 15 people managing to attend the in-person consultation event in the South West.

The in-person consultations did not cover the North of England – Carlisle and Newcastle were completely missed out. For Wales, the North and South are poorly connected so any meaningful consultation would require not just an event in the South but another in the North.

In Northern Ireland no face-to-face consultations appear to be taking place at all and the date of the online consultation was only announced last week.

We have also received concerning feedback about the online consultations and the understanding of those conducting the meeting. One attendee reported:

It was also clear that not all participants fully understood the consultation questions or their implications, particularly those without background knowledge of the benefits system. This raises significant concerns about the quality and reliability of the feedback being gathered. At one point, the facilitator was unable to explain New Style ESA or JSA, and I had to step in to clarify how these benefits work, especially for those who do not qualify for income-related support. It was concerning to witness such a knowledge gap from someone facilitating a consultation on welfare reform.

Although we were told that all feedback would be recorded — even on topics not officially included in the consultation — it is unclear how that information will be used or whether it will influence policy development in any meaningful way.

The impact of the failure to make arrangements for accessible and meaningful consultation meetings

Only having online consultations and/or not having sufficient and/or accessible face-to-face consultations is unacceptable because, as I’m sure you’re aware, at least one-third of disabled people do not have access to the internet or the skills needed to take part in an online meeting. This obviously means that many people who will be most affected by the Government’s planned cuts to social security payments will be totally excluded from taking part in any consultation events.

We are concerned that the consultation not only doesn’t deal with many of the policies that are most likely to affect disabled people (as it only deals with 12 out of 22 policies) but fails to properly engage disabled people on those limited topics. We are also concerned that full impact assessments which would inform engagement with the consultation are not available and will not be made available during the course of the consultation.

The whole process to date seems inaccessible, chaotic and incomplete and given how few people are being consulted, both virtually and in person, we are extremely concerned about how representative this process is and whether it meets even the most basic standards of engagement with disabled people and their advocates.

Furthermore it is DPAC’s view that the whole process is flawed and is non-compliant with Articles 4 (3) and 33.3 of the UN CRPD and General Comment 7.  It also violates the Gunning Principles and the requirements to make reasonable adjustments under the Equality Act and is therefore potentially unlawful.  The only meaningful remedy is to withdraw the proposals and meaningfully engage with disabled people and our representative organisations to ensure all government proposals are compliant with the UN CRPD and equality legislation and ensure progressive realisation of the articles as well as compliance with equality duties.  Failure to address these flaws may result in legal action and sanction from the disability committee of the UN.

It is essential that the government start again on welfare reform, listening to disabled people and carers in a genuine process of co-production.

In light of the concerns outlined above and the limited time available, we invite you within 7 days i.e.  by June 16th to confirm:

1.     What steps are being taken to ensure that online and in-person consultation events are accessible and available to affected disabled people across all relevant regions. This should include ensuring accessible venues, across a range of regions as well as adequate notice to allow for attendance arrangements to be made.;

2.     That the time for engagement with the consultation will be extended by at least 4 weeks, to reflect the delays in making accessible arrangements and allow meaningful engagement with disabled people.

We look forward to your response by June 16th.

 

Linda Burnip

On behalf of the DPAC steering group

c.c. Debbie Abrahams, Chair of the Work and Pensions Select Committee,

Katie Farrington, Director General Social Security, Disability and Pensions

Helga Swindenbank, Head of Disability Services

Jun 032025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The DWP have cancelled the only in-person consultation event on the disability cuts for the whole of Wales, and do not plan to run another.

They did this after announcing an inaccessible venue at the last minute, in what we believe to be a clear example of disability discrimination.

The consultation was always going to be unfair, given half the proposals – the most important half – were off the table for discussion on day one.

We are demanding that there must be no vote in the House of Commons on disability cuts until a full and genuine public consultation has been carried out in Wales.

Please sign our open letter, and ask your MP or Member of the Senedd (Welsh Parliament) to sign too. You can sign, and ask your MP to sign, even if you don’t live in Wales.

Below is a template letter for contacting your MP or MS.

Find your MP or MS using WriteToThem, Find your MP, and/or Find a Member of the Senedd (in Wales)

 

Template letter

[Please use this template as a starting point and use your own words as much as possible.]

Dear [MP or member of the Senedd]

 

I am writing as your constituent to ask that you support an open letter demanding that there must be no disability benefit cuts vote in the House of Commons until Wales has had a full and genuine consultation – #NoVoteWithoutWales

The DWP have now cancelled the only in-person consultation event on the disability cuts for the whole of Wales, and have communicated that they do not plan to run another. Instead they are suggesting an online-only event at the end of the month, probably after any vote has already happened. This isn’t good enough.

The DWP cancelled the consultation after announcing an inaccessible venue at the last minute, in what could only be described as a clear example of disability discrimination.

Given the DWP’s failures, any consultation must now be run independently by Welsh disabled people’s organisations.

Please read and sign here:

https://Bit.Ly/No-Vote-Without-Wales

No vote without Wales! #NoVoteWithoutWales

Kind regards,

[Name]

[Postcode]

[Phone number]

May 192025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

We have seen a letter to Liz Kendall signed by 36 loyalist Labour MPs who have formed a group to support the disability benefit cuts.

While the prospect of a cushy junior ministerial role, or the threat of the whips, might persuade many Labour MPs to vote in favour, this list represents some of the worst MPs, who are actively campaigning for the changes.

They should be lobbied and protested. They should not receive a penny of trade union support. They should be challenged at elections. CLPs must pass no confidence votes and trigger reselection ballots.

The list is:

David Pinto-Duschinsky MP
Luke Akehurst MP
Bayo Alaba MP
Jas Athwal MP
Danny Beales MP
Rachel Blake MP
Nesil Caliskan MP
Luke Charters MP
Shaun Davies MP
Jim Dickson MP
Helena Dollimore MP
Graem Downie MP
Damien Egan MP
Allison Gardner MP
Gurinder Signh Josan MP
Andy MacNae MP
Blair McDougal MP
Frank McNally MP
Samantha Niblett MP
Jon Pearce MP
Gregor Poynton MP
Connor Rand MP
Steve Race MP
Joani Reid MP
Mike Reader MP
Jake Richards MP
Tom Rutland MP
Mark Sewards MP
Sarah Smith MP
Mike Tapp MP
Fred Thomas MP
Dan Tomlinson MP
Jo White MP
Sean Woodcock MP
Steve Yemm MP

 

A letter to Liz Kendell supporting the disability benefit cuts. It has been signed by 36 Labour MPs.

Aug 092018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

https://www.independent.co.uk/news/social-care-funding-uk-government-local-councils-proposals-local-government-association-lga-a8470361.html

https://www.local.gov.uk/about/news/lga-launches-own-green-paper-adult-social-care-reaches-breaking-point

 

Have your say on the future of adult social care – respond to the Local Government Association’s (LGA’s) survey.

The consultation, which is the largest ever launched by the LGA, will last for eight weeks and will shape the LGA’s demands ahead of the Budget, due in the autumn.

Izzi Seccombe, chair of the LGA’s Community Wellbeing Board, said: “People have a right to live the life they want to lead and high quality adult social care and support plays an essential role in this. It is also vital to society. It strengthens communities, reduces pressures on the NHS, supports around 1.5 million jobs and contributes as much as £46bn to the UK economy.

“But work to find a long-term funding solution for adult social care and support has been kicked into the long grass by successive governments for the past two decades and has brought these services to breaking point.

“It has created a deeply uncertain and worrying future outlook for people who use adult social care services now and the growing number of people who will need them in the future.”

The LGA has produced their own ‘green paper’ and would like your views on it. Things you might want to consider are -:

  • should care be free at the point of delivery,
  • should it be funded through taxation,
  • should it be delivered by local government or should alternatives be considered,
  • should the postcode lottery be ended and a national system of social care be put in place working in a similar way to which the ILF did.

You may not want to answer all of the questions in this consultation or feel they are all relevant to you but please answer those that you can and ask others to as well. Do also give examples of how the current system is failing to meet your needs either due to charging policies, refusal to provide help with specific tasks or unmet needs you have.

To complete the consultation, please read the LGA’s green paper and then submit your views via the online form, which is available at:

https://futureofadultsocialcare.co.uk/the-green-paper/have-your-say/

 Posted by at 20:10
Mar 082018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Decades after Iceland’s ‘day off’, our women’s strike is stronger than ever

The Global Women’s Strike has evolved into a worldwide protest with myriad demands

Selma James

‘As a result of Poland and Argentina coming together, the International Women’s Strike was formed.’ Women march in New York, 8 March 2017. Photograph: E McGregor/Pacific / Barcroft

 

On the first day of the UN Decade for Women in 1975, the women of Iceland took the day off to demonstrate the importance of all their work, waged and unwaged, in the countryside and the city. Almost all women who were physically able came out of their homes, offices and factories, and even female television presenters were replaced on the screen by men holding children. Some 90% of women took part. They called it a day off but we at the International Wages for Housework Campaign called it a strike, and took as our slogan their placard which said: “When women stop, everything stops.”

 

Iceland was not international but it was of international significance. What moved them to strike had to be moving in the souls of women everywhere: the question was: when would it manifest itself?

 

In 1985, at the final conference of the UN decade in Nairobi, we had won the UN decision that unremunerated work at home, on the land and in the community should be measured and valued. We called Time Off for Women for 24 October and a number of countries joined us. But we could not sustain international action.

 

International Women’s Day: how can you support the global strike?

 

It was not until 1999 that Margaretta D’Arcy, a writer, anti-war and Irish Republican activist, called for a national strike of women in Ireland to mark the new millennium on 8 March 2000 and asked the Wages for Housework Campaign to support her call. I wrote to the National Women’s Council of Ireland, telling them that if they called the Irish women out on strike, we would make it global. They didn’t, but we did. We launched the Global Women’s Strike with Margaretta and women from a number of other countries at the UN in New York in 1999. In most of the 60 countries where women went on strike it was a celebration, not a mobilisation. But we were making a variety of demands. The first was: “Payment for all caring work – in wages, pensions, land and other resources.” What was more valuable than raising children and caring for others, we asked. “Invest in life and welfare, not military budgets and prisons.”

 

The more women went out to work, the harder it was to also be a carer, and what was most galling was the lower pay for doing a double day. Caring and pay equity have risen on the political agenda, as well as other injustices that women face, beginning with rape and domestic violence often going unpunished.

 

Two years ago, two important movements manifested themselves. In Poland women went on strike to stop anti-abortion legislation. They succeeded in getting the government to back down. In Argentina, following police inaction after the rape and murder of a number of women, hundreds of thousands took to the streets with the slogan Ni una menos (not one less). Their call for an end to femicide swept across Latin America and beyond. This spoke to a pervasive injustice – in the UK, for example, two women a week are killed by partners or ex-partners. As a result of Poland and Argentina coming together, the International Women’s Strike was formed last year and co-ordinated by Polish women. It was agreed that each group would determine their own demands. There were regular four-hour Skype calls (with English and Spanish translation) with women from more than 30 countries exchanging information about what they would be doing. In some countries, hundreds of thousands downed tools for some part of the day, had rallies and banged pots; in others, the events were smaller.

 

Selma James and male journalists at the launch of the Wages for Housework campaign in 1975. Photograph: Keystone/Getty Images

 

Today, the idea of women massively withdrawing labour, waged and unwaged, is not a reality yet. The actions now are often overtly anti-racist and anti-every discrimination, anti-poverty, anti-war, anti-deportation and anti-imperialist, including in Trump’s US. They are always anti-violence. In Peru, the strike slogan is: “If our lives have no value, produce and reproduce without us!” Every sector brings its own concerns. Peruvian domestic workers are launching their petition: “A living wage for caring work – in your own home and other people’s.”

 

But how can you strike if you can’t risk being sacked or endangering those you care for? This has always been the dilemma, especially of the carer on whom vulnerable people depend. In countries such as Spain, where there is general recognition of the strike validity and even union backing, it’s easier for women to walk out for at least part of the day – hundreds of thousands are expected to do just that.

 

In the UK, where such support is not yet forthcoming, women can still publicise our situation and what we want changed in call-ins and letters to the press, returning from lunch even 10 minutes late, banging pots in the streets or at the window, as women in Spain did against the 2003 Iraq war.

 

The Global Women’s Strike is putting the family courts on trial for unjustly taking children from their mothers in a speak-out in the shadow of parliament; cleaners are demonstrating for a living wage; there is a sex work strike for decriminalisation in Soho; and a picket of Unilever in support of the Sisters of Rohingya’s call for disinvestment from Myanmar to end the rape and genocide there.

 

In Germany, another possibility to improve women’s lives has opened up, which we are bringing to the strike. Some 3.4 million members of the IGMetall union are winning the right to a 28- (instead of 35-) hour week for at least two years in order to care for children and elderly parents. This is what we can win when striking and care come together.

 

• Selma James is founder of the International Wages for Housework Campaign

www.theguardian.com/commentisfree/2018/mar/08/iceland-global-womens-strike-protest


Global Women’s Strike

www.facebook.com/GlobalWomensStrike/

@WomenStrike

25 Wolsey Mews, London NW5 2DX

020 7482 2496

 


 Posted by at 12:12
Feb 252018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
The Alliance for Counselling and Psychotherapy has organised a demo at the New Savoy conference again this year. It’s an early start at South Kensington.

Wednesday 21st March 2018 from 8.15am!

Millennium Conference Centre!

4-18 Harrington Gardens!

South Kensington, London, SW7 4LH

 

The New Savoy Conference is the annual gathering of professional and

charity bodies providing psychological therapies (IAPT) in NHS primary

care.

IAPT is an assembly-line service providing short-term therapies to over

a million people every year. Despite the commitment of its frontline

therapists and psychologists, IAPT is failing the mental health needs of

communities all over England, while working with government policies

that themselves generate psychological distress and social alienation.

Come and join therapists, mental health activists, psychologists and

welfare campaigners. Meet at the Harrington Gardens entrance of the

Millenium Conference Centre (Gloucester Road tube) from 8.15am to

greet conference goers.

 

Contact info@allianceforcandp.org for more information.

Some context:
• The hierarchy of IAPT and psychological services in the NHS who gather at these conferences continue to offer liberal mouthings about DWP welfare reform policies, WCA and PIP, sanctions, coercion around Work and Health. But they’ve actually taken no real action to boycott DWP/Health collaboration, despite all the developments re judicial reviews, UN condemnations, the recent Parl Committee report, and the UC debacle.
In his intro to the conference, in the programme link above, Jeremy Clarke (NS chair) says:
“The second issue is the running sore of welfare benefit reform, and its negative impact on mental health, that undermines whatever benefit we make to population wellbeing. Have we reached a consensus now for how we can turn the tide? The BBC’s Mark Easton will find out”
• The overall theme is depression; there are sessions on the crisis in the IAPT workforce, latest staff survey, impact of targets; session on Work and Health Unit; Wessely’s review of human rights and compulsory treatment; session on Employee Assistant Programmes (often run by people like Maximus); familiar faces in the list of speakers
•The scam of IAPT as a service in local communities. It has a massive evidence base, tons of statistics for every CCG in England including “recovery” rates; ethnicity stats; deprivation stats; etc etc No-one really analyses the figures. For IAPT it seems just collecting the stats is their claim to being evidence based and therefore their claim for funding from the Government. In fact, their stats reveal a shockingly failing provision.
For example, ot of 1,350,000 referrals a year 85% either never enter any kind of therapy, or never finish a course of treatment, or don’t “move to recovery” (as IAPT jargon has it). In my CCG (Tower Hamlets) only 6.6% of referrals to IAPT “recovered” and among the Bangladeshi community who make up over 30% on TH population only 3% “recovered”. Farmer’s Taskforce target for % of population who “need IAPT therapy” is 15%, rising to 25% by 2021. In TH about 2% of the pop were referred/referred themselves to IAPT, of whom as I say 6.6% “recovered”.
IAPT will be a major part of the propaganda around the NHS reorganisation now in progress, via the STPs and the ACOs they are developing . STP management have “the mental health crisis” high on their agenda – certainly their PR agenda – and selling more provision for IAPT services will be a major plank of the campaign. See Hunt on this role for IAPT here.
IAPT is rarely taken to task as a service that is massively failing communities all over England. This is true in the Labour Party as much as any where ekse. This has to stop. It is a propaganda service for neoliberal capitalism and its dissemination of psychological scapegoating and coercion across society
 Posted by at 16:27