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

I whole- heartedly congratulate the hon. Member for Eltham and Chislehurst (Clive Efford) on the customarily forthright and direct way in which he opened the debate. I agree with all the points he made; he would expect that of me, as his loyal deputy on the all-party parliamentary group. It is great that we have heard so many solid and significant contributions today. Once we are a couple of hours into a debate, we start to get a feeling for how it is going, the emerging themes and the sense of direction. We all acknowledge and appreciate the huge progress that has been made. When I started out on this campaign more than 20 years ago, I would never have believed that we could get to this point, at which payments are being made to those impacted and those affected. The Minister is starting to hear that the same issues are emerging. Constituents are experiencing the same complications and difficulties, and the same representations are being made. I will not touch on those, because so many have been raised, but I might just reinforce some of the points made. The Minister is beginning to hear a chorus of things that need to be addressed—and addressed they must be. We are on the cusp of having something of which we can be proud—of this House having addressed one of the biggest scandals that we have ever experienced in parliamentary life. We took control of it; we handled it; we got a report and an inquiry; and we got billions of pounds of compensation. We have the opportunity to pay that compensation right now, and I hope that the Government grab it. I pay tribute to IBCA for the work that it has done. It is amazing that we have put together the infrastructure and a support scheme as quickly as we have. IBCA has done remarkable work in such a short time. It is starting to deliver, and I think we are all immensely pleased and proud that this House has collectively been able to construct it, and to make sure that it is functional and works. I have visited IBCA on a couple of occasions, and I have met the staff and discussed many of these issues with them. I recognise their sheer dedication to the work that they are pursuing, in the best interests of everybody whom they serve; and their commitment, as an arm’s length body. It is amazing that we have got here, but it was not always like this. I remember what happened back in the early 2000s. I am looking at the chair of the APPG, my friend the hon. Member for Eltham and Chislehurst, and he will remember this, too. We were fobbed off, disregarded and lied to when we took up the cases of our constituents. They presented to us at our various surgeries with these unexplained difficulties and complications. They would say, “How did I get HIV?”, or “I’ve got hepatitis. I do not know how on earth this happened.” We would write to successive Ministers in the Department of Health, making representations, and asking for assistance or acknowledgement, only to be told that they were not interested, and that there was nothing to see here. They would say, “Move along. We are not prepared to take this up. Believe me, we are doing everything in our power, and there’s really nothing to acknowledge.” For years, we were fobbed off and disregarded, and for years, we fought on. Over the years, I have got to know the campaigners. They came together with a common purpose, determined to get to the heart of the issue and to support each other. We call them the community, and we could not find a better community than the campaigners who have led this, been at the forefront, and refused to accept “No”. They are people with different lives from different backgrounds, but they all carry the burden of what happened to them. All of them are still here, fighting the good fight, determined to get justice for the whole community, and that whole community is the key thing today. I was the APPG chair for all those years, and the community has some of the finest people I have ever encountered. I have seen lots of campaigns in this House, and I have seen how people approach these issues, how they take them forward, how they engage and how they access their Members of Parliament to make sure that things are done. It is the most fantastic campaign we have ever had. Unfortunately, I could not make the ceremony at St Paul’s, as I was recovering from an illness, but I know from friends, colleagues and campaigners who were there the importance to them of that ceremony, where they were recognised as a community for their work. There have been high points, and we should acknowledge that. Few of us would have expected Theresa May to have made the announcement back in 2017 that there was to be a full inquiry. A lot of us were surprised that she chose Sir Brian Langstaff to lead it, and lead it he did. Like many people in this debate, I listened to lots of the evidence in the inquiry sessions, and I cheered along with the community when the report was produced. I was in this House when the report was launched, and the Government took full responsibility and said that there would be a full repayment scheme and that people would get what they should. Those were great days, met with real enthusiasm and euphoria by those who have campaigned. There have been good days, but we have to address the biggest issue. It has been mentioned on several occasions, so I will not labour the point, but people have been waiting decades. Even at this point, the majority of these people are still waiting just to start their claim. That is not to receive compensation—we might think that we would be at that stage now—but just to get into the system. Even at this stage, only a relatively small number have been paid. People have mentioned that these are real people—people who are unwell and who know that time is not on their side. I do not know which Member mentioned it, but people are dying weekly because they are not having their situation attended to and their payments made. Families still have no clarity about when their case will move forward. That is made worse by what is being asked of them. I have been surprised—I have listened carefully to colleagues who have raised this—that we see people being asked for evidence that in many cases simply does not exist. They have been asked for records from decades ago, such as proof of cohabitation between parents and children in the 1980s. Those things were probably never properly recorded in the first place, and if they had been, it may have been lost over time. That means that so many people are being delayed or sometimes shut out completely because they cannot meet requirements that are not realistic. In some cases, people run into a purely arbitrary administrative date, rather than when harm was actually suffered. Members have mentioned the bereaved families in whose cases support can stop at the point of death rather than reflecting the full impact of what has been lost. Another theme that has developed—I think it was the right hon. Member for New Forest East (Sir Julian Lewis) who raised this in particular—is the growing concern about those with hepatitis C who were treated with interferon. That has to be addressed. Of all the issues that have started to emerge, that is the one that the community in general wants us to press as strongly and as directly as we can with the Minister. I hope that we get some satisfaction.

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