Pete Wishart

Pete Wishart

Scottish National Party — Perth and Kinross-shire

Speaking in the House of Commons on 18 June 2026

Debate

Infected Blood Compensation Scheme

Contribution

Interferon was introduced as almost like a chemotherapy drug back in the day, and some of its impacts and consequences have been similar to the side effects and impacts of chemotherapy. Physically and mentally, the effects are often severe and long-lasting. When the Minister is on his feet, perhaps he can explain a little more about what he intends to do with this group and this community. The Government have introduced a new level 2B to recognise some of these harms, and my understanding is that it provides a temporary uplift, but it seems to apply only in certain circumstances. What it does not seem to do—I have read about it carefully—is reflect the long-term reality for many. The argument appears to be that the higher category covers just about everything else when it comes to interferon treatment for hepatitis C, and that levels 3 and 4 already take interferon into account. My colleagues in Haemophilia Scotland asked for the evidence showing how that was factored in, and none was provided, so can the Minister tell us a more about that evidence in relation to levels 3 and 4? A similar set of concerns relate to unethical research, as we have heard. The Government have expanded eligibility and increased awards. That is welcome in principle, because it means that people are recognised without having to jump over additional evidential hurdles, but there is still a lack of clarity as to whether the level of award properly reflects what actually happened to people. The issue seems to be the arbitrary 1985 cut-off date. Perhaps the Minister can provide clarity. Officials say that there is no evidence of unethical research beyond that point, but the inquiry itself referred to evidence beyond that date, and even up to the 1990s, of children being recruited without proper information or consent. Why did the Government arrive at 1985 as a cut-off date for eligibility for unethical research awards, given that there is evidence that unethical trials and research continued well into the 1990s? There are also ongoing concerns about estate claims, because the structure of the payments could disadvantage those who died earlier, and about unpaid care over the years. That, again, has been reflected by several hon. Members. A few people referred to some of the different schemes around the devolved nations. I am particularly proud of what we did in the Scottish Parliament, and the Minister will be aware of the bespoke schemes across the whole United Kingdom, not just in Scotland. The one that particularly worked in Scotland—I want the Minister’s response regarding what has happened to it—is the special category mechanism known as the severely affected category. This was open to people who had significant problems and issues; they could apply, and were given an increased payout and support. That has since been subsumed under the general supplementary scheme; that scheme is welcome, but this is disadvantageous compared with the superior scheme in Scotland. Those who were initially on that superior scheme have been kept on it, but those who wished to apply for it have to go through bigger hoops and hurdles to get there. We need to know that scheme will still be available and that it will be easier for people to apply to it, because we were particularly pleased about the way it operated in Scotland. Let me turn finally to accountability. Throughout the decades, the Government repeatedly dismissed those asking questions and trying to achieve justice. The final report acknowledged that the infected and the affected were fed lies and lines, and that serious concerns were dismissed outright. We have to address this. We cannot leave it. We have to look at how we get round some of the things that were encountered. I remember the letters I got from various Government Ministers: “The Government do not accept that any wrongful practices were employed and do not consider that a public inquiry is justified.” I got that for years, every time I raised these issues on behalf of a constituent. I listened carefully to the infected blood inquiry. The evidence I found most compelling was from a certain Andy Burnham, who was Health Minister at one point during that period—I believe he is in the news today for some other reason, not particularly related to this. I remember Andy Burnham candidly telling the inquiry that he now knew that the lines he had been given by senior officials in the civil service were wrong, and that he had sent lies to me and other Members who raised these issues in Parliament. That is what he said, in effect, in evidence to the inquiry. That is simply unacceptable. The current Ministers are probably much better than their predecessors, and will look carefully at what comes across their desks, but this must not be allowed to happen again. That is why we need a statutory duty of candour on all public officials, including civil servants and senior civil servants. More than that, we need an independent compensation body to oversee all Government compensation schemes. Such a body would retain expertise and experience, would save time and money when schemes are set up, and would be capable of ramping up and down according to need. The Hillsborough law must be enacted without delay, introducing a duty of candour for everybody involved in public life. A national oversight mechanism should be established to monitor and scrutinise the implementation of recommendations from all public inquiries and hold the Government to account. After all this, it is hard to believe that the first meeting I had about the issue was back in about 2004, with a lovely lady from Blairgowrie, in my old constituency. She came to see me in what could only be described as a hell of a state; she could not account for why she had HIV following a blood transfusion after a medical emergency. It was because of her that I started to get involved in all this, tried to find answers and tried to ensure that campaigners got justice. The name of that lady was Tricia Titheridge. After contracting HIV, she died in 2013, without seeing the huge progress that we have made. It is because of people like Tricia that we are all still here—still fighting to ensure that everybody is included and that there is a scheme that works for all our constituents. Looking at the Minister and knowing the qualities that he will bring to this job, I am pretty certain that he is going to be the man who delivers this for everybody, meets our concerns and looks at the difficulties we have presented today.

More from Pete Wishart

Other recent Hansard contributions by the same speaker.

About Hansard

Hansard is the official verbatim record of proceedings in the UK Parliament. Every word spoken in the Commons and Lords is recorded and published — this page is a single contribution from that record.

For Pete Wishart's full parliamentary record including voting history, expenses and all other contributions, see the Pete Wishart report card.

Partner sites