Universal Credit and Personal Independence Payment Bill

Ann Davies Excerpts

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

[Ann Davies (Caerfyrddin) (PC)]

I stand to support new clauses 8 and 11, and amendments 12, 38 and 39, among others, which I will mention as I go through my speech. I promise to keep to the unofficial four-minute time limit.

A week after the cruel Universal Credit and Personal Independence Payment Bill and its arbitrary eligibility cut-offs was first discussed, we are today being asked to amend and pass this deeply flawed Bill in a couple of hours. Of course, it is now a completely different Bill from what was first introduced—even the title will be changed. I am not alone in welcoming the removal of clause 5, which means that no one will lose vital personal independence payments so that the Government can save some money. However, unlike other hon. Members, I do not believe that the UK Government’s concessions make the Bill any more worthy to become legislation.

The Government have conceded that placing an arbitrary cut-off date on PIP eligibility is unsupportable, so why on earth do they continue to do exactly that for claimants of the health element of universal credit? I commend the hon. Member for Leeds East (Richard Burgon) for amendment (a) to amendment 2, which would keep the health element of universal credit at £423.27 for all new claimants, rather than lowering the rate for people who are unlucky enough to require that support after 2026, which will cause real hardship. The Joseph Rowntree Foundation estimates that, without further changes, over 700,000 disabled people will still face a cut to their income of up to £3,000 a year by 2030.

We do not know what data has informed that approach or how it will impact on the great people of Wales. An assessment of the specific impacts on Wales has been necessary since the UK Government first announced their welfare cuts months ago. Now that their plans have changed considerably, that impact assessment is all the more crucial. People in Wales need transparency and certainty about how the changes will affect their lives.

In what functioning democracy does a Government Bill get fundamentally altered in the middle of the first debate on that very Bill, and then elected representatives are given only a few hours to scrutinise it before it is passed? We need time to scrutinise the Bill fully and effectively. We need time to co-produce it with the constituents whose lives it will affect. This is a chaotic and shameful state of affairs, especially in the light of the substantial impact that the Bill will have on thousands of disabled people on the lowest incomes.

[Mr Joshua Reynolds (Maidenhead) (LD)]

Will the hon. Lady give way?

[Ann Davies]

I am just coming to the end of my remarks, if the hon. Member does not mind. I am keeping to my four-minute time limit.

The Bill should be scrapped. It is neither fair nor compassionate welfare reform. It is not fit for our constituents.

[Graeme Downie (Dunfermline and Dollar) (Lab)]

I will speak to amendment 17, which I tabled with the support of 62 Members from across the House. It would ensure that if a person has a fluctuating condition such as Parkinson’s or multiple sclerosis, that is a factor in considering whether they meet the severe conditions claimant criteria.

I have been working with Parkinson’s UK, and as the new chair of the all-party parliamentary group on Parkinson’s, I have heard concerns from those living with the condition, and their carers and families, about the problems they already face in accessing support through the welfare system, because of fundamental misunderstandings about the fluctuating nature of the condition. Those concerns have been exacerbated by the Bill, particularly paragraph 6 of schedule 1, which states that in order to meet the severe conditions claimant criteria,

“at least one of the descriptors…constantly applies.”

Someone with Parkinson’s, MS, ME or other similar conditions may be able to carry out one of the activities in the descriptors such as walking for 50 metres or pressing a button in the morning, but then not be able to do so by the afternoon. Under my initial reading of the Bill, that means that someone with Parkinson’s could never be a severe conditions criteria claimant because they would not meet the descriptor “constantly”.

I thank the Minister and his team for their extensive engagement with me on this matter, but the language used in the Bill has caused concern and fear for those with Parkinson’s. As the Minister has helpfully said, and as he explained to me prior to the debate, much of the explanation that I have received centres around existing guidance that a person must be able to undertake the activity in the descriptor “repeatedly, reliably and safely”. If they cannot, the criteria will count as applying constantly and they will be considered a severe conditions criteria claimant.