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—