Universal Credit and Personal Independence Payment Bill Debate
Full Debate: Read Full DebateStella Creasy
Main Page: Stella Creasy (Labour (Co-op) - Walthamstow)Department Debates - View all Stella Creasy's debates with the Department for Work and Pensions
(2 days, 14 hours ago)
Commons ChamberIt is a pleasure to take part in this debate.
The Bill is being rushed through by a Labour Government desperate to paper over the cracks in an economy that they themselves have brought to a shuddering halt. So many of the questions that are coming before the House at the moment are the result of that economic flatlining and the flailing of a Government who are casting around desperately to see how they can get themselves off that economic hook.
Put simply, the Bill is unaffordable. The Prime Minister’s latest concessions to his unruly Back Benchers—now happy and victorious—have left the Exchequer with a £5 billion gap to plug, which inevitably means higher taxes for hard-working families who are already feeling the pinch. Far too few of those voices will be heard today. Too often in debates in this House, Members are consumed with the idea that more spending is a better thing that can always be afforded, and therefore no responsible decisions need to be made. That was the decision of the Labour Back Benchers who wrested from those on the Front Bench control of one of the flagships of this Government’s agenda, leaving the Government—massively endowed as they are with Members of Parliament—like some gigantic ship that has lost all power and propulsion, listing at sea, waiting for the next wave to come along.
As we in this Chamber know, the next wave that comes along and buffets this Labour Government from the left comes all too often from the hon. Member for Walthamstow (Ms Creasy), to whom I am happy to give way.
I absolutely agree with the hon. Lady that we should consider such people. I think of the lady who came to see me on Saturday at my street surgery. She was concerned about the brutality of the PIP process and the way that she and her husband, who has a degenerative, progressive disease for which there is no cure, are put through the wringer to justify their situation, which anyone with any common sense would see deserves support. But the hon. Lady will be aware of the mushrooming in claims from those with various levels of mental health challenges.
Ultimately, we must balance looking after people with degenerative, progressive diseases in a humane and civilised manner with making sure that we have a system that cuts out fraud, and that seeks to minimise those who do not need aid seeking it and getting it. If only we could have a system in which people did not claim for money that they do not deserve and need, we would be able to look after the people whom I think—this is one area of commonality between the hon. Lady and me—both she and I would agree require fairer and more generous treatment.
At Committee stage, we often table amendments to try to understand the nature of the legislation. Many questions are being put forward in this concertinaed process. The first is whether we should make policy by phone-in rather than on an evidence base. That is the only justification I can see for new clause 12 tabled by the Opposition, who appear not to understand that no recourse to public funds guides the lives of many migrants in our community. It contains a fundamentally un-British perspective on people who come here and work for many years in our national health service, and who then have a stroke or perhaps develop MS. Under the Opposition’s proposals, we would deny such people the support they have paid into as taxpayers. It is a dog whistle so loud that I fear the dogs in Battersea right now are having a terrible time. We should not make policy by phone-in but by evidence, and I pay tribute to the incredible words of my hon. Friends the Members for South West Norfolk (Terry Jermy) and for Beckenham and Penge (Liam Conlon), who bring their own experiences to this debate.
I will speak to new clause 4, which I tabled, as well as to other amendments. Those amendments come from my experience of what makes good policymaking in this place and from my concern that we need to protect our constituents from the vagaries of public policy. I think in particular of a 62-year-old constituent of mine who is physically disabled with a mobility condition called ankylosing spondylitis—I will tell Hansard how to spell that. She works full time and lives alone in a rented flat that has been adapted for her. Removing, messing around with and playing with her benefits—as this Bill would do for millions of people around this country—will not save money; it will simply cost more. My constituent would struggle to get to work and to look after herself, which she can do using the welfare support that she gets under the current system. That means we will face higher costs in the long run.
I wish that Members would learn from the evidence on the bedroom tax. The bedroom tax was brought in under the same metric that we heard from the right hon. Member for Beverley and Holderness (Graham Stuart), who is no longer here—that somehow people who are supported by our welfare system are probably making it up. This is not a moral argument I am making; the bedroom tax did not save the money it was meant to save, because it just pushed costs into other parts of the public sector. That is why it is so important that agree to new clause 4 and weave the principles of the UN convention on the rights of persons with disabilities into this legislation. It should be guided by principle not prejudice—in particular the principle that we should respect our fellow human beings and our constituents who have a disability.
New clause 4 covers the question of co-production, and on this point I am sorry that my hon. Friend the Member for Penistone and Stocksbridge (Dr Tidball) is not in her place. I want to come back to that question, because there is a very important principle about co-production that we have not bottomed out, and I want to hear from the Minister about it. There is a simple premise that we signed up to in the UN convention, which I hope Members across the House would support, that there should be an adequate standard of living—that is identified in article 28. Crucially, article 19 also sets out that there should be an independent living process for our disabled constituents. That is why in 2017, 2024 and indeed 2025, when the UN criticised the previous Government, we rightly held them to account for it. What do we wish for our disabled constituents, if not an independent and equal standard of living? What do we wish for them, if not the basic human right to be treated equally? We must recognise that the world we live in does not work for them, and we must account for that through our welfare system so that they can live freely and, yes, play a part in the world of work while also living with dignity.
It is about very practical things, such as the freedom that comes from someone having a carer who helps them get dressed so that they can go to work. That is supported by our welfare system. It is also about travel costs, especially for those living in my constituency, where Transport for London seems to be hellbent on breaking down all of the stations so that they are not accessible. Covering those costs means that someone can go out to see family and friends. There is also the food that someone might need if they have a condition like phenylketonuria—a metabolic condition that means a person needs a low protein diet. These are not equal experiences, but by using our welfare state to support those people, we can have ensure that they have the human rights we wish them to have.
New clause 4 is about giving due regard to the principles set out in the UN charter so that benefits are calculated in a way that means they are sufficient to allow people to live a life of freedom equally alongside their fellow human beings. The payments we make must meet those tests so that disabled people in our communities can meet their living expenses. That is a question that many hard-working people who are struggling at the moment in their lives can recognise well.
It is about levelling the playing field. It is not, as the right hon. Member for Beverley and Holderness said, about making fools of us all. Those are principles that I hope the Government will commit to weaving throughout the legislation. That is why new clause 4 matters: it goes beyond the principle of co-production, which I know the Minister has recognised, to the basic principle of how we treat people. That would apply to the universal credit health element of the Bill. If we restricted a benefit, it would call on us to ask why we consider somebody to need X amount at this point in time but Y amount in the future, and to ask whether that will live up to the required standard of living.
I want to touch on co-production in particular. Many have talked about it, but people do not necessarily understand what it means. It is not consultation. Co-production means that whoever is included can say no as well as yes. Without a power of veto, all we have is a better managed consultation. Co-production genuinely empowers every participant to shape things, because they can walk out of the room as well as being part of it.
The Minister has talked about seeking consensus, but it is not an equal relationship if disabled people are not given the clear power to veto what is put on the table, such that the Government have to work with them so that they do not use their veto. That is the principle of co-production—that is why it is not consultation—and that is what we should be seeking.
I have much sympathy for new clause 8—I am sorry that my right hon. Friend the Member for Hayes and Harlington (John McDonnell) is not in his place—because I was here in 2015 when George Osborne used statutory instruments to slash the tax credits that our constituents relied on and 3 million people were pushed further into poverty. I was also here when MPs on both sides of the House expressed frustration about the use of that process. We had to watch the House of Lords clear up our mess and stand up to the Chancellor for using delegated legislation to take £1,300 away from our constituents. I hope the Minister will understand that this is not about this individual Bill or even about his good intentions; I know that he has engaged with all of us. It is about the principle that if we are to change the law, we should be able to amend and adjust that law and scrutinise it on behalf of our constituents.
My hon. Friend the Member for Sheffield Hallam (Olivia Blake) set out many alternative ways in which we could switch spending to invest in order to save money in the long run. There are many different ways in which we can support our economy to grow; it does not have to be off the backs of our disabled constituents. There is also the important principle here—I know many on the Labour Benches believe this—that socialism is the language of priorities. Our priority must be to empower and enable every single one of our constituents to achieve their potential—and yes, that happens through a growing economy, and also through a welfare state.
I hope that the Minister will address the amendments that seek to ask questions about how we get this right. For many of us those unanswered questions are troubling —we cannot bring back answers for our constituents—because they tell us that we may not achieve those things that I have set out. None of us who have lived through George Osborne and the bedroom tax ever want to go back to that again. We want to be able to say to our constituents, who might find themselves in the position of the father of my hon. Friend the Member for South West Norfolk, that we can absolutely be proud of the system we are building today, just as we are proud of my hon. Friend himself.
I rise to speak in support of new clause 11 and amendment 38. I am incredibly relieved that the Government have listened—most importantly, they have listened to the people who will be affected by changes to PIP—and taken clause 5 out of the Bill. The terms of reference for the Timms review have already been set without involving disabled people, but there is a chance with new clause 11 to ensure that it moves forward in a truly co-produced way. What worries me is that without the proposals in the new clause, the Bill highlights the need for co-production but provides no assurances that it will be comprehensively done. Disabled people must feel that any changes to the welfare system are made properly with them rather than done to them.
I have walked in the shoes of families in my constituency bringing up children with special educational needs and disabilities. For decades, my son and I have been caught up in the endless cycle of assessments, mandatory reconsiderations and tribunals. That is a situation familiar to many who have turned to the DWP for help to manage life with a disability or disabilities.
This is the reason that so many disabled people are terrified of the Government’s proposed changes: the DWP is too frequently at war with the people it is supposed to protect. Too frequently, it lets down the most vulnerable in our community, and it mostly gets away with it. Recently, the incredible Joy Dove won an eight-year legal fight to link her daughter Jodey Whiting’s suicide to the stopping of her benefits, which the DWP admitted was a mistake. Jodey’s avoidable death is not the only one.
DWP decisions often seem to be completely arbitrary. Once, when I was waiting to go into a tribunal, I received a call from the DWP offering to reinstate my son’s benefits if I dropped the tribunal. That experience cemented in my mind something that I believe to this day: the culture of the DWP is hostile to disabled people. That culture must change if we are to have any chance of building a sustainable, fair and compassionate welfare system for the future.
A constituent of mine in Scarborough and Whitby suffers from a variety of complex physical and mental health conditions, including PTSD, attention deficit hyperactivity disorder, anxiety disorder, polycystic kidney disease and liver disease. In May, after reporting a deterioration in his health, he submitted new evidence to support reassessment for a higher rate of PIP, which led to the DWP removing his award entirely. He was left with no income or support despite his ongoing need for care.
This is the reality: many disabled people who are turned down for PIP rely on the health element of universal credit. Many of my constituents have fluctuating conditions, such as MS, ME and mental health conditions. The reality of their conditions means that during periods of remission they return to employment. However, once their condition deteriorates, they return to universal credit. If that happens, with this Bill they would return on a lower level than before, down to just £50 a week. That completely ignores the realities faced by disabled people and their experience of their conditions. Without the protections provided for in amendment 38, we would create a two-tier system where people with unpredictable conditions would be valued less than those with more predictable ones.
I urge hon. Members to support new clause 11 and amendment 38. I also ask the Government to please pull the Bill. Even at this late stage, let us get it right for the people who really matter; let us get it right for disabled people.
Let me make just a little more headway. I will give away a little bit later.
As my hon. Friend the Member for Penistone and Stocksbridge and I have discussed, I do not agree that the review must be finished within 12 months. We want to complete the review by autumn of next year, and with no four-point threshold, I do not think it is in anybody’s interest to rush it. I accept her proposal, in subsection (4) of her new clause, for a group to co-produce the review, not so much to provide independent oversight as to lead and deliver it. I will chair the group, and we will work with her and others to include disabled people with lived and professional experience in its leadership and in shaping its meetings, with around a dozen members and with capacity to engage others as needed on specific topics.
My hon. Friend has made helpful suggestions for who some members of the group might be. We will want disabled parliamentary representation to be involved in the process as well, and arrangements to involve disabled people more broadly. I agree with her that the majority of the group’s members need to be disabled people or representatives of disabled people’s organisations, and that they need to be provided with adequate support, including towards their costs of travel and taking part.
The hon. Gentleman raised that point very reasonably in the debate, and it is certainly something we need to consider as well.
I welcome the commitment to work with disabled people. The Minister will know that the difference between consultation and co-production is that every participant has to have a veto of the outcomes in order to co-produce. Otherwise, with the greatest will in the world, it is just another form of consultation. Can he give us an assurance that disabled groups will have a veto over the proposals, to engage the consultation process?
We will aim for a consensus among all those taking part, and that is what I hope we will achieve.