Universal Credit and Personal Independence Payment Bill

Alison Bennett Excerpts

2nd reading
Tuesday 1st July 2025 Commons Chamber

[Alison Bennett (Mid Sussex) (LD)]

I want to begin today not with statistics or slogans, but with the reality of just one life: a constituent of mine, Sarah, from Hassocks. Sarah has a spinal cord injury. She is a wheelchair user, and this is what her personal independence payment makes possible.

It pays for underwear that does not dig into her skin, wedge pillows to raise her legs, grabber sticks, so that she can pick things up off the floor, and a second wheelchair to keep upstairs. It covers the use of a specialist rehabilitation gym that keeps her as healthy as possible. It allows her to buy heated blankets for the cold weather, because the cold weather makes her pain worse. It pays for specialist outdoor clothes from Norway to cover her legs, and in hot weather, it pays for extra fans, because the heat makes her injured body swell.

Sarah’s PIP funds a CPAP—continuous positive airway pressure—machine that runs 24 hours a day, connected directly to the hospital, because she has developed sleep apnoea, and it pays for the additional electricity to keep it going. It pays for a specialist mattress to prevent pressure sores, bathing aides and specialist body wipes for when cleaning herself is just too difficult. It pays for extra fuel for an average of four medical appointments each month, some in Hassocks and some as far away as London, and it has helped to make her garden accessible so that there is at least one part of her home where she feels free. These are not luxuries; they are the bare essentials that allow Sarah to live in dignity, with some measure of independence.

Sarah told me she has no faith in the system operated by the Department for Work and Pensions and no trust that fair and just decisions will be reached, because in her experience, the DWP’s overriding drive is not to understand but simply to cut.

[Deirdre Costigan (Ealing Southall) (Lab)]

I wonder whether the hon. Member has told her constituent, Sarah, that under these proposals, nobody who is currently on PIP will have a single penny of their income cut, and they will be protected for time immemorial.

[Alison Bennett]

I did not need to explain that to Sarah—she fully understands that—and I am about to address that point.

The Government’s last-minute climbdown has brought Sarah no comfort, because she never imagined she would be in a wheelchair. She never thought her life would change forever in an instant, and she knows that for thousands of people, that change is still to come. Life can turn on a sixpence—a single diagnosis, a single accident—and suddenly we find ourselves in a world we never imagined, up against barriers we never thought we would face. When that happens, the welfare system should be there to support us, not abandon us.

It is not just disabled people themselves who will be harmed by this Bill; it is also the millions of family carers—the unpaid carers—whose labour sustains our entire health and social care system.

[Rachel Gilmour (Tiverton and Minehead) (LD)]

Does my hon. Friend share my concern about the fate of unpaid carers, given that carer’s allowance hinges on a disabled person receiving PIP? With one in five people in my constituency who are disabled, which is well above the national average, should the Secretary of State commit to delinking carer’s allowance from PIP eligibility, or as a minimum, to providing automatic transitional payments during PIP reassessments, so that devoted carers are not left destitute while assessments drag on?

[Alison Bennett]

My hon. Friend makes a wise point. In my constituency of Mid Sussex, one in four carers are themselves disabled. Carers UK has warned in the clearest possible terms that the Bill still risks a severe and lasting financial impact on future unpaid carers and disabled people—people already facing significant hardship. Even after the Government’s partial concessions, around 81,000 future carers stand to lose support by 2029-30. That is not a small technical change; it is a decision that will push families closer to poverty, create a two-tier system of entitlements, and deepen inequalities.

Let me be clear: the Government have produced no impact assessment, no comprehensive evidence of what this will mean, and there has been no consultation with carers themselves. Carers have been ignored by the Government throughout this entire debacle, and their voice must now be heard loud and clear. The Liberal Democrats will continue to oppose the Bill, which risks stripping thousands of carers of vital assistance, and leaving some of the most vulnerable people in Britain without support. Yes, we agree that the welfare bill is too high, but if the Government were serious about bringing it down, they would be serious about fixing health and, critically, social care at pace, tackling chronic ill health at its root, rather than punishing those who live with its consequences.

Sarah told me that she wanted to speak up not for herself but for that future community of disabled people. In truth, most able-bodied people think that they understand disability, but until someone is there, they cannot comprehend the world of barriers that are thrown up. For many, that day will come after this Government’s reforms have been forced through. That is why I say to Ministers that they should pause the Bill and go back to the drawing board. They should consult the people whose lives they are about to upend, and show them the basic respect of listening before they legislate to take away their support. If we do not stand with disabled people and carers now, and if we do not insist on compassion and fairness at the heart of our welfare system, we will all pay the price later, not just in higher costs to the NHS and social care, but in the erosion of the values that bind our communities together.