Universal Credit and Personal Independence Payment Bill

Caroline Voaden Excerpts

2nd reading
Tuesday 1st July 2025 Commons Chamber

[Mr Morrison]

I wholeheartedly agree with my hon. Friend.

As I have said, many of my constituents have raised their fears, worries and anxieties about these plans. As they have been unable to provide their own stories directly because of the Government’s lack of consultation, I want to use my time to be their voice. Amy from Bramhall suffers from ME, and her illness can fluctuate hour to hour and day to day, making it hard to pass assessments for support. Amy recently appealed to me for assistance after the DWP withdrew her PIP, despite the fact that her illness was getting worse. Amy said:

“It is astounding how I can be reduced to zero points from receiving higher levels for mobility and daily care when I have not been cured nor had any improvement in how my conditions affect my life. In 2018 when my PIP was downgraded, following appeal it was rewarded back to me. Yet, now, without improvements to how I am affected it has been completely stopped.”

Those who have had to face mandatory reconsideration will know the extent of the documents needed and the stress involved, but to cope with this when someone is ill and suffering every single day is simply not sustainable. Amy has been advised that the mandatory reconsideration will take 15 weeks, which is almost four months, so where will Amy get the support she needs during this wait? This situation highlights the barriers that people with chronic illnesses and disabilities face when trying to get support.

[Caroline Voaden (South Devon) (LD)]

Does my hon. Friend agree that these changes risk devastating consequences for people living with complex mental health conditions? They may not score four points on a single activity, but experience persistent moderate challenges across many areas, and this could in fact lead to financial hardship and worsening mental health, which will put more pressure on other services and negate the point of the exercise in the first place.

[Mr Morrison]

I thank my hon. Friend for that incredibly important point. Whether it is motor neurone disease, blindness, ME, arthritis, mental illness or cancer, these barriers will only be further entrenched should the Bill be passed.

Disability Stockport is a local charity that specialises in autism and mental health. It has told me that it is deeply opposed to the changes the Government are proposing:

“Such cuts would exacerbate poverty, worsen mental health issues, and further reduce the already limited support available to the most vulnerable and marginalised people across Greater Manchester. We believe this would pose a serious risk of harm.”

While Disability Stockport welcomes the Government’s investment in employment support, it is clear that much more is needed, because of people such as Joan.

Joan lives in Cheadle Hulme and worked in financial services before falling very ill. She explained to me the persistent and defeating barriers that disabled and ill people face when trying to secure employment. She faces a six-month wait for an assessment for Access to Work. How can this Government expect more disabled people to work if they have to wait six months just for an assessment? Joan told me that it is a degrading process to have to work without adjustments. She has to push herself through pain and fatigue, because she does not receive sick leave during her probationary period. If Joan moves jobs, she will have to start over again, despite a registered record of her need adjustments. This is just one example of the lack of full and effective investment in supporting disabled and chronically ill people into work.

The Greater Manchester Coalition of Disabled People has told me it is concerned about those using PIP to pay rent and bills. It also expressed the view that this rushed legislation does not truly apply more pressure on or give more support to employers to make accommodations for disabled people. Instead, the Bill will protect the status quo, and the onus to get support will be on the individual, not the employer. It asked:

“What will happen to 16-22 year olds who no longer get Disability Living Allowance and don’t quality for PIP?”

These young people will fall through the cracks and be pushed into poverty.

By bringing forward this Bill, which could amount to the biggest cut to sickness and disability benefits in a generation, it is clear that there is no sense of the real-life impact it will have on hundreds of my constituents and hundreds of thousands of people across the constituencies represented by Members of this House.