Universal Credit and Personal Independence Payment Bill

Debate between Robin Swann and Zarah Sultana

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

[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 Only two tins of fish four years out of date remained.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.