(9 months ago)
Commons ChamberThe House will be surprised to know that I will talk about not billionaires, but ordinary people in my constituency of Kingston upon Hull North, for whom this Budget provides very little.
The Budget also provides very little investment, which we desperately need in Hull and the Humber. It exposes the reality of what levelling up actually means for the north as we come to the end of this Parliament. It is trifling; it is not transformative. The Chancellor mentioned Canary Wharf. That is not an area in need of levelling up. The Hull and East Riding devolution deal comes with headline-catching funding of £400 million, but it is spread over 30 years. That is £13.3 million a year shared between two councils. That comes nowhere near reversing Hull’s loss of £111 million a year since 2010. That stands in direct contrast to the Government’s economic transformation and integration deal with Rwanda, which comes with at least £370 million over five years—an average of £74 million a year—for levelling up in Rwanda.
I will focus mainly on what is not in the Budget: any compensation for the infected blood victims. That is despite the fact that 118 Members of Parliament from 10 parties wrote to the Chancellor last week, asking him to make an announcement on the allocation of funding for those people, and it comes after this House defeated the Government in December by voting to set up a compensation body through the Victims and Prisoners Bill.
I congratulate my right hon. Friend on her excellent work on the contaminated blood scandal on behalf of all our constituents. Does she agree that it is heartbreaking for children to have watched their parents go through this?
(1 year, 5 months ago)
Commons ChamberI beg to move,
That this House has considered the Infected Blood Inquiry.
I thank the Backbench Business Committee for granting the debate, ensuring that this important issue is considered on the Floor of the House. Over the years, it has been incredibly generous in allocating time to Back Benchers in our attempt to hold Ministers and the Government to account on the infected blood scandal. I also thank the Father of the House, the hon. Member for Worthing West (Sir Peter Bottomley), for working with me to secure the debate and with whom I am proud to co-chair the all-party parliamentary group on haemophilia and contaminated blood. I thank all right hon. and hon. Members who are here today and who have fought so hard for their constituents who have been infected and affected. I know of many other MPs who are not able to attend the debate today but support our work.
In opening, I want to say a few words about three individuals among the thousands who have been affected by this scandal, to remind the House of the people at the heart of this debate. First of all is my constituent, Glen Wilkinson. In 2010, he came to see me at my last surgery before the general election. He told me how he had been infected by dirty blood given to him by the NHS. Along with thousands of others, he wanted to know how that was allowed to happen and he wanted a public inquiry. I promised to try to help him if I was still an MP after that general election. It was a very close run thing and I ended up with a majority of just 641, so I was fortunate to be returned. I joined the all-party group and have been very proud since then, with Glen, to fight for truth and justice, not just for him but for all those who have been infected and affected. Of course, we did secure the public inquiry in 2017. Glen is still campaigning for justice despite his health problems, but I know that, as the years have dragged on, the need to keep fighting has exerted enormous pressure on him, his wife Alison and his wonderful family. At this point, it is worth remembering all those family members and pay tribute to those who have been caught up in this scandal.
A few nights ago I could not sleep—it is very hot—and I ended up going online. I read the witness statement to the public inquiry by Nick Sainsbury, whom I had met through Glen and who lived in East Yorkshire. Nick attended the Lord Mayor Treloar College as a child and was one of dozens of children at the school infected with HIV and hepatitis through infected blood products. We know that 72 of those pupils later died. After school, Nick worked as a civil servant and then at the Land Registry, which he said was his dream job, until his mid-30s when he became ill from multiple viral infections. He had to give up his job. He said:
“It was just too much. I was going to work bent double on crutches.”
I want to quote what he said about being HIV-positive in his statement to the inquiry:
“The knowledge that I was infected with arguably the most feared infectious disease since the bubonic plague of the middles ages was hard enough to deal with. The constant reminders on TV and in the newspapers made it very grim.”
Nick campaigned for years for justice. He travelled to many meetings here in Parliament, and attended and contributed to the public inquiry. But just two months ago, Nick sadly died, never having seen justice.
I also want to mention Michele, who currently is not represented in Parliament by a Member of Parliament, but wanted me to raise her case. Michele Claire was given a contaminated blood transfusion following childbirth and consequently developed hepatitis C. She now has stage 6 liver disease. After people in her village found out about Michele’s infection, she received letters through her door saying things like, “We don’t want your type round here”. On compensation, Michele told me:
“Money can cure nothing. It will, however, bring about some dignity and ensure peace of mind going forward.”
My message to the Minister is this: it is time. Action to fully compensate those infected and affected by the contaminated blood scandal must start now. The Government have accepted that compensation should be paid and that there is a moral case to do so.
I am sure the whole House will agree with me that my right hon. Friend has done a sterling job in campaigning on this issue for a number of years. Will she join me in paying tribute to Della Ryness and her husband Dan, who sadly passed away last month, who fought the good fight on behalf of their son, who died from this very awful thing, and in thinking about the beautiful granddaughter who he left behind?
I am very grateful. This is about people. It is about mums and dads, sons and daughters, and aunts and uncles. We have to remember that. It is about those individuals and their families.
(8 years ago)
Commons ChamberI am very happy to agree with my hon. Friend. That should certainly be investigated.
I return to people’s concerns about the use of private companies. We know that, over the past six years, there has been a huge sense of mistrust of the disability assessment regime operated by Atos before it walked away from its contract with the Department for Work and Pensions. If there is one thing that could fatally undermine progress towards a better support scheme, it is the plan that the new scheme be administered by a private company. I strongly urge the Government to look again at that plan and show empathy for the people affected.
I congratulate my hon. Friend on her dogged and tireless work on this issue. Does she agree that there is a big issue of trust here, in relation not just to the potential new providers but to what happened previously? Some survivors and families who survive victims who have passed away believe that senior health professionals knew about the contamination but decided to continue with their interventions for cost reasons.
Yes. One point I will come to later is the need for some form of inquiry.
To continue my point about why who runs the scheme is so important, a big criticism of the new scheme is the continuation of discretionary payments. Department of Health officials are still not listening to the concerns raised about that. The APPG inquiry uncovered huge issues with the highly conditional and poorly managed discretionary support scheme. One respondent told us:
“The whole system seems designed to make you feel like a beggar”.
I also believe that the trust’s current administrators have not fought hard enough for their beneficiaries, which legally they could have done. Instead, they saw their role as dispassionate managers and conduits to the Department of Health. They left the affected community alone to fight for themselves. If the new support scheme ends up being managed by Atos or Capita it will do nothing to address those fundamental issues, and could even make the situation much worse, adding insult to injury. I call on the Minister to do the right thing and announce that she will scrap plans for a private profit-making scheme administrator, and will replace the current scheme with a more beneficiary run and focused organisation that has no profit motive.
Will the Minister set out exactly what kind of discretionary support the new scheme will provide? It remains unclear whether any or all of the current support will continue. That contrasts starkly with the Scottish scheme, where the financial review group agreed that no one should receive less financial support under the new scheme. Will the Government urgently provide the same guarantee and publish full details of any obligations that the new scheme administrators will be subject to?
There are also issues with the current welfare benefits reassessment regime that many people are having to go through—for example, moving from disability living allowance on to the personal independence payment. Those issues need to be addressed urgently, so that individuals can be passported straightaway on to new benefits. I hope the Minister will agree that that is a sensible way forward for the people affected.
My third concern relates to the families of those affected, who need better support under the scheme. Under the new English proposals, widows and widowers will continue to be eligible for discretionary support—whatever that means; I have raised my concerns about that already—on top of a new £10,000 lump sum, provided their loved ones died at least partially as a result of contracting HIV or hepatitis C. However, many clinicians have already told me that that could mean many people are excluded from assistance simply because their partner’s death certificate does not include mention of HIV or hepatitis C, sometimes at the family’s request. The new proposals could also still be considerably less generous than the support that some widows already receive, because there is a huge question mark hanging over what discretionary help they will get under the reformed scheme.
I agree with my right hon. Friend, who makes his point very well. We need to make sure that any new support scheme moves quickly. We need to get on with this. The previous Prime Minister, when he apologised on behalf of the nation 18 months ago, also allocated £25 million, but none of that has been spent yet, as I understand it. We need to make sure that a scheme is introduced as quickly as possible, although obviously with our concerns having being addressed. But absolutely the two things can run in parallel, and a Hillsborough-style panel inquiry would give people the opportunity of a truth and reconciliation inquiry. I still think it a key requirement if there is to be any real sense of justice and closure.
Families who have suffered a loss following this terrible scandal have expressed a desire to get hold of certain documents and to find out what happened and who knew what. They really just want a sense of justice.
I will now conclude. I know that in later speeches hon. Members will want to raise the deeply moving stories of their constituents. It is those stories that have led me to campaign on this issue over many years, and I am always mindful of the struggles faced by my constituent Glen Wilkinson. Glen was diagnosed with hepatitis C after a routine tooth operation in the 1980s, when he was just 19. He has had to live with the virus all his life and is still waiting for proper recognition of how it has affected him. I hope that the Minister and the Government will now work to ensure that Glen and others can live the rest of their lives in dignity.