Infected Blood Compensation Scheme

Debate between Pete Wishart and Nick Thomas-Symonds

Wednesday 23rd October 2024 Commons Chamber

[Pete Wishart (Perth and Kinross-shire) (SNP)]

It is a pleasure to follow the hon. Member for Eltham and Chislehurst (Clive Efford). In me, he has another willing volunteer to assist him in the group, as he knows. He is absolutely right to pay tribute to our former colleague, the right hon. Member for Kingston upon Hull North and Cottingham (Dame Diana Johnson), who led the group with such distinction and energy in the last Parliament. She was almost personally responsible for ensuring we had the legislative solution to take forward the compensation schemes.

I also pay tribute to the right hon. Member for Salisbury (John Glen), who made a significant difference when he took leadership on this issue for the last Government, after years of obfuscation, delay and dithering. The right hon. Gentleman got to grips with the matter and all the campaigners recognise what he brought to the role. I hope that this Minister does the same. We all acknowledge that he has made a good start. The points that the hon. Member for Eltham and Chislehurst makes as chair as the all-party parliamentary group on haemophilia and contaminated blood are absolutely right. If he continues in that curious and investigatory style, we will continue to encourage the Government to do the right thing by the infected and the affected.

I am happy to say, with a great deal of satisfaction, that we have made significant progress. We are at the point of being able to deliver the scheme, and we will start to see payments to those who have needed support and compensation so badly throughout all these decades. My only slight criticism of the right hon. Member for Salisbury is that it is a pity that we did not get the opportunity to debate the issue in the last Parliament. There was an unsatisfactory statement from the former Prime Minister, who then just disappeared. There was no real opportunity to ask questions properly. I know he made an effort to address some of the concerns, but it would have been good to hear more at that point about how the schemes were being taken forward. The general election created a massive gap, after all the energy and activity that had been summoned up to resolve the issue, but we are where we are.

The final report by the infected blood inquiry was a fantastic piece of work. I pay tribute to everybody involved in it. They went about their jobs diligently and comprehensively, and we ended up with a wide-ranging report that shed a dramatic light on all the things that had gone wrong. It paved the way to create a positive way forward that is now beginning to deliver.

We must remember why we are here: thousands of people were caught up in probably the worst health scandal this country has ever endured. It is a failure of the British state that we ended up in a situation where people, through no fault of their own, contracted HIV, hepatitis B and hepatitis C. When those who were caring for them raised concerns, they were constantly ignored and told, “There’s nothing to see here.” The inquiry was unequivocal that a compensation scheme must be set up immediately. The regulations we are debating today are essential for delivering that compensation scheme as quickly and effectively as possible.

I have been supporting victims of the infected blood scandal for about 20 years, since it was first brought to my attention by a constituent, who died about 10 years ago and is no longer with us. I remember the frustrations of those early years when I was constantly writing on behalf of this constituent just to be stonewalled—to be told that there was nothing to see and nothing further to be considered. It was that reluctance to take these issues seriously that defined those early years.

I said to the former Minister, the right hon. Member for Salisbury, that I hoped we would get some sort of separate investigation into why Members of Parliament were consistently deceived and—I shall say this—lied to by people working in the Department of Health. We were constantly writing letters on behalf of our constituents, and the replies were clearly rubbish. As a recipient of several of those letters from Ministers, I want to know why I was deceived in the way that I was. I pay tribute to Andy Burnham: he recognised this and he actually signed many of those letters as the former Health Secretary. I want to know how this came to his desk and why he actually did this.

The key thing is, as other Members have said, that the groups that are representing the community are properly listened to and are engaged in the construction of the regulations. It is too late for the regulations we are debating, but when it comes to the affected, the representative groups have to be central to the design of the new regulations. I say that because they have real life experience of this matter. They know what the issues are. They have fought for decades to get to this stage to secure this justice and compensation. I know that there is frustration. I saw the Minister screwing his face in response to the hon. Member for Eltham and Chislehurst, but those groups do feel frustrated. They feel that they are being ignored, that their concerns are not being taken seriously, and that they are getting generic general replies from the Minister instead of detailed, proper responses to their issues.

[Nick Thomas-Symonds]

rose—

[Pete Wishart]

I will give way to the Minister if he will explain to me exactly why that is happening.

--- Later in debate ---

[Nick Thomas-Symonds]

I just want to say that the hon. Member should read nothing into that facial expression. When I close this debate, I shall talk in detail about the consultation that has taken place. That includes the extensive consultation that Sir Robert Francis undertook during the election campaign—the period between me and the right hon. Member for Salisbury being in office. That was hugely important. The Government have listened and have made significant changes to the scheme. It is not about giving generic replies, as the hon. Member has suggested. The Government will continue to move extremely carefully and listen to concerns, and the Infected Blood Compensation Authority will do the same.

[Pete Wishart]

I am to grateful to the Minister for his response. I look forward to his summing up, as I know that he will sincerely try to address these matters, but I say to him that all I am doing is reflecting the concerns that I have heard from the groups that I have worked with so closely over the years. There is a sense that they are not being taken all that seriously and that they are not getting the responses and the information that they think are important.

The Minister mentioned Sir Robert Francis. There has been nothing other than glowing praise for the way that Sir Robert has carried out his business. I know that he had a useful and productive meeting with representatives of Haemophilia Scotland where everything was aired and properly discussed. There is absolutely no complaint from anybody in this House about the way that Sir Robert Francis has gone about his business. He has been up and down the country listening to the groups. But there are certain things that only the Minister can respond to, particularly when it comes to policy decisions. That is why I encourage him to hold a debate on them. He has said that he is prepared to do so, which I am grateful for, and that he has perhaps been misunderstood. The community must be given the information and advice that they require.

There are a couple of matters that I hope the Minister will address in his closing remarks. I will not repeat some of the points that have already been raised, as I know he has taken a note of them. Sir Robert Francis proposed an additional autonomy award under the supplementary route for those who had been subjected to the unethical treatment and experiments that have been described. Although that is welcome, it is not clear how the figures have been arrived at, so I would like a little more clarity on that. How have these figures been calculated?

One issue that possibly has not been raised today is those with hepatitis C who were treated with interferon. Early treatment methods for the eradication of hepatitis C had many negative side effects, which were extremely difficult to go through and had a lasting effect on those treated. Is that a group that the Minister will consider?

The future operation of support schemes is also important. The decision to continue existing support scheme payments for life for those who were registered with a scheme before 1 April 2024 was a welcome development. The House will know how important that is to me as a Scottish Member of Parliament, as we had a very effective, productive and useful support scheme that I think will now be concluded and no longer open to new members. I would like to hear a little more on that point.

Sir Robert’s report said:

“The benefits offered by the scheme to eligible recipients for financial and other support services should be no less than those offered by any of the current support schemes.”

I want to know whether that is still the Government’s position. It is also assumed, based on Sir Robert’s recommendation, that all the benefits of the support schemes will continue. It would be good if the Government could confirm their position at an early date so that individuals have clarity on their future entitlements.

Under the regulations, the Minister has the power to make arrangements for the provision of support and assistance to applicants or potential applicants for compensation under the infected blood compensation scheme. Sir Robert Francis has identified three groups to which the Minister might usefully apply that prerogative: IBCA-funded legal representation, IBCA-funded financial support from an independent financial adviser and IBCA-funded legal support to executors of estates where there are complex matters to resolve in determining entitlements and access to an independent mediation service.

My hon. Friend the Member for Aberdeenshire North and Moray East (Seamus Logan) spoke about the need to ensure that representative groups are properly supported and resourced to continue their vital advocacy work on behalf of so many in the community. I would like the Minister to say a little more about the willingness of the Government to ensure that those groups are properly funded. The effort that they have put in over decades—sometimes in a solitary exercise by two or three people—is extraordinary and should be recognised as part of the scheme.

We are looking forward to the next round, and it is important that we go forward. I have queries, which I know the Minister will probably address, about why only 20 people have been contacted, as the hon. Member for Eltham and Chislehurst mentioned. I have no idea why it is only 20, so perhaps the Minister can tell us a little more about the rationale. It is right that the system be tested to see whether it is robust before it is opened to a wider community, but he has to say a little more about why it is those 20.

I am not having a go at the Minister, who I think is doing a good job; I am here to congratulate him and encourage him ever so gently to get moving just that little bit faster. We have had decades of obfuscation, a lack of progress, and people dying as they waited for compensation. This matter now sits on the Minister’s shoulders. We will be watching him and keeping an eye on it. I know that there will be regular updates to the House. Believe me, we will all be here to ensure that he is doing the right thing by the victims.

House of Lords (Hereditary Peers) Bill

Debate between Pete Wishart and Nick Thomas-Symonds

2nd reading
Tuesday 15th October 2024 Commons Chamber

[Nick Thomas-Symonds]

I cannot comment on the coherence of the Opposition in the course of that process. What we have seen so far is a pretty incoherent effort, but perhaps it will improve when we hear from the shadow Minister.

This Bill is about making immediate, long-overdue progress. The House of Lords existed for centuries as a nearly entirely hereditary House. There was an attempt to introduce life peers as long ago as 1869, with a further attempt to introduce life peers and remove the hereditary element in 1888. Despite those efforts, it was only with the passage of the Life Peerages Act 1958 that non-judicial life peers began to join the other place.

Some 40 years later, a Labour Government introduced a Bill to end the right of hereditary peers to sit and vote in the House of Lords. The events that smoothed the Bill’s passage led that Government to accept an amendment on the principle of the removal of hereditary peers. The amendment retained 92 hereditary peers on a temporary basis, until further reforms to the other place were brought forward. Despite attempts at further reform, that temporary measure is still in place.

[Pete Wishart (Perth and Kinross-shire) (SNP)]

One of the dates the Minister missed was Labour’s pledge, which has stood for over 100 years, to abolish the House of Lords. That pledge was reiterated by the Prime Minister only a couple of years ago. Is it still Labour’s intention to abolish the House of Lords? Does he understand the cynicism about further progress, given that the pledge has not been honoured in over a century?

[Nick Thomas-Symonds]

I cannot comment on the hon. Gentleman’s cynicism about progress, but our manifesto clearly sets out the Government’s position, which is that we should have an alternative second Chamber that is more representative of the nations and regions.