Universal Credit and Personal Independence Payment Bill

Robin Swann Excerpts

2nd reading
Tuesday 1st July 2025 Commons Chamber

[Robin Swann (South Antrim) (UUP)]

I rise to support the reasoned amendment and to vote against the Bill, which will produce an abandoned generation: young people with disabilities and life-limiting conditions who are currently on children’s disability living allowance and who would normally transfer to PIP at the age of 16. The Bill completely ignores them and forgets about them. The usual process is that around someone’s 16th birthday, the DWP sends them an invitation to claim PIP, and it is then up to the parent or young person themselves to apply, within a time limit of 28 days. This Bill does nothing to address that. It is a process of mandatory self-application, so there is no automatic conversion for a child with a disability or a life-limiting condition who is already entitled to DLA to move on to PIP.

The stricter eligibility criteria in the Bill and the concession actually make it worse, because as of November 2026 new PIP claimants must meet the four-point single activity daily living test. For those young people with a disability or life-limiting condition who are currently in receipt of children’s DLA who would normally have transferred to PIP, come November 2026 their condition must be such that it enables them to reach that four-point eligibility test. Those young people, who this place and the devolved legislatures keep talking about and encouraging to stay in education and be supported with their special educational needs, are now being told that, come 16, if their condition does not meet the four-point criteria, they will not be in receipt of personal independence payment. That payment is a door opener for their families and allows them to access carer’s support. It allows those young people, if they look to further their education or employment, to access mobility and support schemes. It allows those young people with disabilities and life-limiting conditions to hope and to dream, and to be eligible for support to enter the workforce. If a young person who, come November 2026, does not have a condition that allows them to reach that four-point criteria, that payment will be denied to them.

[Mr Adnan Hussain (Blackburn) (Ind)]

I want to share the words of young disabled children from my constituency. They said to me this weekend, “Don’t speak for us, speak with us.” That struck me, because so often in this place decisions are made about people without ever really listening to them. Does the hon. Member agree that if we are serious about a just and compassionate welfare system, we should honour those words, “Don’t speak for us, speak with us” and, better still, listen?

[Robin Swann]

I thank the hon. Member for that intervention. I have met these young people, too. I met people from an organisation called BraveheartsNI, which represents a cohort of young people with congenital heart defects who are at that transitional stage. They told me about the real concerns—they are not just concerns, but fears—among these young people, who have been looking forward to the opportunity to go to university, get on to training courses and seek employment but still require additional support.

Mencap has highlighted that child DLA is the main childhood disability benefit for children aged nought to 15. Some 166,000 children with learning disabilities, autism and Asperger’s retained or increased the total monetary value of their child DLA award when transitioning to PIP. Mencap is concerned that this number will decrease because of those young people not being able to achieve the four-point eligibility criteria.

For the sake of those young people who have special educational needs, disabilities and life-limiting disabilities, who we all come to this place to support—to give them a future and to give them hope—I implore the Government to withdraw this Bill now, go back, engage and co-produce something that meets the needs of our country and our young people.

[Several hon. Members rose—]

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[Paula Barker (Liverpool Wavertree) (Lab)]

Let me start by saying how shocked I am that the Minister has intervened, near the end of the debate, to say that he will be removing the whole of clause 5 from the Bill. While I am grateful for the concessions, this has further laid bare the incoherent and shambolic nature of the process. It is the most unedifying spectacle that I have ever seen. As the House has just heard, we will vote tonight on the Bill as it stands on the Order Paper, and not as amended. I am really sorry to say this, but when it is not written down, it is not worth the paper it is written on. We were promised a Hillsborough law by April this year, and nothing has come to fruition.

[Robin Swann]

Will the hon. Member give way?

[Paula Barker]

No, I will not.

It is with sadness that I will vote for the reasoned amendment tabled by my hon. Friend the Member for York Central (Rachael Maskell), and I will vote against the Bill. I implore my Government to do the right thing: to pause, take a breath, and let us get this right.

Before entering Parliament I had served local government, the trade union movement and working people throughout my life. Service matters deeply to me, and I see it as my job to do exactly that as a Member of Parliament. I am a passionate believer in the dignity of labour and of secure, well-paid work being the route out of poverty and to opportunity and a life free from fear, but this Bill, I regret to say, will create poverty, and has already induced fear.

I think everyone in this House believes that we need to reform our welfare system, but we must be honest: the Bill before us today is not reform. It is simply cuts, which have been brought forward to fill an economic black hole. In the Liverpool city region, nearly 30% of residents are disabled—more than 10% above the national average. Liverpool has one of the highest disability rates in the country, and our region already experiences some of the highest poverty rates in the UK.

Even with concessions, this Bill still entails cuts, not reform. It will see 150,000 people pushed further into poverty, and create a stark disparity in our welfare state for disabled people. Despite a commitment to co-production, there is nothing that commits the Government to ensure that the PIP assessment review’s findings have any bearing on this legislation.

Over the last few weeks, we have heard a lot about the lack of time to scrutinise legislation when debating another Bill in this place, yet here we are with a Bill that has concessions that are not actually on the face of the Bill because there has been no time. There will only be eight days between Second and Third Reading, which is truly a lack of time to scrutinise proposed legislation.

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[Ann Davies (Caerfyrddin) (PC)]

I have heard some really passionate, personal speeches in the Chamber today, and I thank all hon. Members for their testimonies and contributions.

The Universal Credit and Personal Independence Payment Bill is a direct attack on ill and disabled people, just to cut costs. Arbitrarily restricting eligibility for PIP, and cutting the health element of universal credit, will have devastating and lasting consequences. Whatever this Labour Government claim, there is neither fairness nor compassion in their approach to welfare. It is certainly not fair or compassionate for the people of Wales, who will be disproportionately impacted by these measures.

I thank organisations such as Policy in Practice and the Bevan Foundation for their vital work in filling the absence of data for Wales, which the UK Government have all but refused to provide. Four of the 10 local authorities that are worst hit by the welfare cuts are in Wales, impacting on 6.1% of the Welsh population at a cost of £470 million for our communities. In Carmarthenshire alone, the economic impact will be nearly £17.5 million, and too many people will suffer. My constituents will suffer.

[Robin Swann]

I just want to make a point of clarification. The hon. Lady mentions that her constituents will suffer. The Government have withdrawn clause 5, but under clause 6 the legislation will still apply in Northern Ireland. Are the Government going to put a barrier down the Irish sea with regard to PIP?

[Ann Davies]

I will allow the Minister to answer that in his closing statement. I could not possibly comment.

My constituent Clare Jacques has several disabilities, including arthritis. She currently receives PIP, which has helped her to build on her master’s degree in equality and diversity in work and allowed additional support, such as the ability to have a carer accompany her when necessary. Ms Jacques does not have four points in any one part of the daily living component. Versus Arthritis has calculated that 79% of people who claim PIP in Wales for arthritis alone score fewer than four points, which is nearly 17,000 people.

This is not just about claimants. Mencap, which has been mentioned, has estimated that over 13,000 carers may lose their carer’s allowance in Wales due to caring for people with fewer than four points. The Government’s justification for this suffering is completely flawed. The Joseph Rowntree Foundation has found that 60% of recipients scoring four or fewer points are already in employment in England and Wales, rising to 63% in my constituency of Caerfyrddin.

The UK Government claim that their amendments to the Bill will lessen the blow—we will have to wait until after Second Reading to see them—but they are set to penalise people who become disabled after the arbitrary cut-off date of November 2026. What data has informed these concessions, and what specific evidence suggests that people can pick and choose when they become sick or disabled, because that to me looks like discrimination? Legal experts for the Equity union agree that it could be

“unlawful on the grounds of arbitrariness.”

Such arbitrariness looks half-baked considering the PIP assessment review will be published only in autumn 2026.

The UK Government’s amendments to the Bill do not address the fundamental injustice at the heart of these measures. Is plunging 150,000 people into poverty rather than 250,000 really a marker of success? Is only punishing people who will get ill or disabled in future, or those who turn 18 later, really a sign of a fair and compassionate welfare reform? I call on hon. Members across this House, and particularly my friends on the Labour Benches, to vote against this cruel Bill. The Labour UK Government must abandon these damaging plans entirely, and instead create a welfare system founded on dignity, equity and compassion, and one developed with disabled people and representative organisations. Plaid Cymru Members will be voting for the reasoned amendment moved by the hon. Member for York Central (Rachael Maskell) and against the Second Reading of the Bill.

Universal Credit and Personal Independence Payment Bill

Robin Swann Excerpts

Committee of the whole House & 3rd reading
Wednesday 9th July 2025 Commons Chamber

[Robin Swann (South Antrim) (UUP)]

I fully agree with the hon. Member on co-production and co-designing any changes that come forward. Does she agree that it is crucial that young people are also included, given the conditions that they can face, and especially given the challenge in moving from children’s disability living allowance to the personal independence payment, which the Minister has still not addressed?

[Siân Berry]

I thank the hon. Member greatly for that intervention. When I have gathered together young people in my constituency, I have found that the issues that they face are unique, and their voices absolutely must be heard.

The Government have said that they are committed to co-producing the Timms review with disabled people and disabled people’s organisations, but organisations such as Disability Rights UK have told us that those promises are hard to trust. They fear a tick-box exercise, co-production in name only, and that the Government’s original plans will be the inevitable result. That is why I have signed up to new clause 8, tabled by the right hon. Member for Hayes and Harlington (John McDonnell), as well as new clause 11, tabled by the hon. Member for Penistone and Stocksbridge (Dr Tidball).

If clause 2 and its schedule remain, the severe conditions criteria simply cannot stand as written. It appears that the Government either meant to exclude people with fluctuating lifelong conditions such as Parkinson’s or multiple sclerosis from the higher rate of the universal credit health element, or that Ministers completely overlooked that community when rushing all this through. Criteria that withdraw support from people with fluctuating conditions are unacceptable, and that is why I signed amendment 38 tabled by the hon. Member for York Central (Rachael Maskell), and amendment 17 tabled by the hon. Member for Dunfermline and Dollar (Graeme Downie). The severe conditions criteria also say that any diagnosis must be made in the NHS. Again, that is either careless drafting or a deliberate restriction, so I have also signed amendment 33 from the hon. Member for Aberdeen North (Kirsty Blackman).

I am trying to bring to this House the voices of disabled people in Brighton Pavilion and across the nation who are closely watching what we do today. So many of our constituents remain scared by the Bill. Right from the day of the sudden and careless release of the Green Paper, which contained terrifying policy details that were not in the Labour manifesto, they have been forced into a cruel limbo. It is shameful that the Government have chosen this path. This Labour Government are showing themselves far more willing to punish disabled people than ask the most wealthy to shoulder the burden of fair public spending on real social security.

I am so proud of the people power that has been brought to bear on the Bill. Action by disabled people and their allies has forced MPs to listen and take action, and forced the Government to withdraw the most brutal cuts, but still the Bill remains unacceptable without the serious amendments that I have outlined. I look forward to hearing much sense, including what the United Nations has told us, from the many hon. Members in this debate who share my values. My Green colleagues and I are ready to do all in our power to minimise the consequences of the Bill; to make it do good, not harm; and ultimately, if that does not happen, to see it fall. I hope the Government will truly learn from the cruel mess that this has become.

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[Zarah Sultana (Coventry South) (Ind)]

I rise to speak in support of amendment 2(a) tabled by the hon. Member for Leeds East (Richard Burgon), amendment 38 in the name of the hon. Member for York Central (Rachael Maskell), amendment 39 in the name of the hon. Member for Brighton Pavilion (Siân Berry), and new clause 8 tabled by the right hon. Member for Hayes and Harlington (John McDonnell).

Errol Graham was a 57-year-old grandad and former amateur footballer. When bailiffs came to evict him, they found his emaciated body in a freezing flat—no gas, no electricity and no food. Only two tins of fish four years out of date remained. He weighed just four and a half stone. A coroner ruled that he had suffered death by starvation. Errol suffered from severe social anxiety. The Department for Work and Pensions knew that, and still cut off his only source of income. As his daughter-in-law said,

“He would still be alive. He’d be ill, but he’d still be alive.”

His death was not a tragic exception; it was a political consequence.

In 2017, Jodey Whiting took her own life after missing a fit-for-work test while she was hospitalised. Stephen Smith was denied benefits despite being gravely ill. He died in 2019. These are not just names; they are the human cost of decisions made in this place—decisions that, according to Sir Michael Marmot’s research, contributed to over 1 million premature deaths in England between 2011 and the pandemic, driven by poverty and austerity. Today the Government press ahead with more of the same.

Clause 2 of the Bill will slash the universal credit health element—the limited capability for work and work-related activity component—from £97 to just £50 a week. By 2030, that is an annual cut of £3,000 for over 750,000 disabled people. These are not people waiting for an assessment; they are people who the DWP has already found too ill to work—people who cannot feed themselves, who live with degenerative illnesses and who experience daily pain, confusion and incontinence—and we are supposed to believe that this is about helping them into employment. Even the Government’s own figures show that fewer than one in 10 new claimants will be protected by the so-called severe conditions criteria, and charities such as Scope, Z2K, the MS Society and Inclusion London have made that clear. The clause will exclude “huge swathes” of severely disabled people, especially those with fluctuating or progressive conditions, such as multiple sclerosis, bipolar disorder and Parkinson’s. Why? Because to qualify, their condition—according to the Bill—must affect them not severely or overwhelmingly, but constantly. As Scope put it,

“It feels like it’s been designed to cut support—not to support people.”

Let us not forget the requirement for an NHS diagnosis in the middle of an NHS backlog crisis. That excludes people with neurodivergent conditions and others who rely on private or social care support. This is a deliberate narrowing of the safety net. The result? A two-tier system that punishes people for trying to work, having variable symptoms or falling through the cracks of bureaucracy.

[Robin Swann]

The severe conditions criteria and the need for an NHS diagnosis exclude young people as well, because their diagnosis and condition may not automatically transfer from their medical records as a child to their adult records. They would need another NHS diagnosis to move from the children’s DLA to PIP.

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[Graeme Downie]

I know that the thoughts of Members across the House are with my hon. Friend and his family. I know what a challenging time it has been, and the fact that he has been able to carry on his duties extensively, representing his constituents, is to his credit and something that his family will be incredibly proud of.

As I said, the Minister has been generous with his time, and I do not believe for a moment that his intention is to restrict access to the severe conditions criteria for those with Parkinson’s. Those words from the Dispatch Box are incredibly helpful, but I ask him to ensure that he keeps a close eye on the situation.

[Robin Swann]

As the hon. Member knows, I signed his amendment, but may I caution him before he accepts the Minister’s very kind guidance? Will he clarify that it is guidance? This is training documentation and it is subject to change. It is not contained anywhere in the Bill or the amendments, so what the Minister read to the Committee was simply training guidance.

[Graeme Downie]

Again, I understand from my helpful conversations with the Minister that this is taking existing guidance and applying it to law, but I understand the hon. Member’s concern.

My final point is to ask the Minister to keep this issue under active review. If any new evidence comes to light to show that the primary legislation is acting as a barrier to the Government’s position being reflected in reality, I hope he will consider opportunities to correct that in due course. We all hope that the Government’s clear intention that people with Parkinson’s and other conditions are in no way—