Contaminated Blood

Debate between Andrew Gwynne and Mims Davies

Tuesday 12th April 2016 Commons Chamber

[Andrew Gwynne]

My right hon. Friend is absolutely right, and I will come on to that point later. We owe it to the victims and their families to find some kind of justice for them.

I am not frequently on the same side as the editorial line taken by the Sunday Express, but I congratulate that newspaper on its tireless campaign for justice. This scandal has seen families torn apart through death and illness caused by the negligence of public bodies. I am willing to accept that, over the years, the response of Governments of all colours has just not been good enough. When the consultation was published in January, I was clear that while no amount of money could ever make up for the impact that this tragedy has had on people’s lives, the victims deserved some form of justice. We have three days until the consultation closes and I want to use my remarks to push the Minister on four points relating to the current proposals.

First, in the 1970s and 1980s, around 7,500 people were infected with hepatitis C or HIV as a result of this scandal. Many of those people were being treated for haemophilia. The viruses have had a devastating impact on their lives and those of their families, not least through loss of earnings and the cost of treatment. The failure of successive Governments to accept liability for this issue means that many of the victims have lost financial security through no fault of their own.

[Mims Davies]

Will the hon. Gentleman give way?

[Andrew Gwynne]

I am afraid that I will not; I do not have enough time now.

The current system of support is only partial; it does not offer the full and final settlement that those affected and their families need in order to live with dignity. Indeed, it falls well below the level of support available in the Republic of Ireland.

We must be honest that the development of support, financial or otherwise, for the victims has been haphazard over the years, and support is always delivered too slowly. However, I remain concerned about aspects of the Government’s proposals. A number of those affected have made it clear to me that removing discretionary payments will make them worse off, potentially by thousands of pounds a year. It makes little sense to announce more funding for a reformed scheme only to remove the critical day-to-day support that so many people rely on. I wrote to the Minister a few weeks ago on that point, so she will know that this is a basic issue of fairness and openness. The victims of the contaminated blood scandal deserve better than this, so I will be grateful if the Minister confirms what is intended for the future of the payments.

Secondly, I welcome the introduction of support for people at stage 1, as so far they have been denied the annual payments to which they should be entitled, but I want to ensure that the impact that a person’s illness has had on other areas of their lives, such as employment or educational opportunities, will be taken into account. Many people have had their professional lives cut short or have missed out on higher education, so I hope that the impact on quality of life will be considered as a fundamental part of the settlement. Furthermore, an assessment every three years strikes me as excessive given that, generally speaking, these conditions will not improve. Many beneficiaries will be receiving either employment and support allowance or personal independence payments and will be regularly assessed for them, so it is unnecessary and punitive to impose a further layer of assessment on the victims. Why not have some form of joined-up approach with the Department for Work and Pensions to make life easier?

Thirdly, I am concerned about the plans to freeze the existing annual payments. Many victims of the scandal had promising careers cut short or were not given the chance to embark on one after being infected. They had that taken away from them in the most damaging of circumstances, and it is just plain wrong of the Government to fail to recognise the loss of standard of living, as well as the effects on health and longevity.

Finally, I want to mention the discrepancies between the responses of the Scottish and UK Governments. As we have heard, the Scottish Government will increase annual payments for those with HIV or the hepatitis C virus, increasing the initial lump sum from £20,000 to £50,000. Will the Minister elaborate on what alignment there might be with the English system?

I do not doubt the sincerity of the Prime Minister when he made a pre-election pledge to do more after the publication of the Penrose report, nor that of the public health Minister, who is doing her best with a constrained spending envelope, but I am sure that she will understand the real disappointment that people have been feeling. This drawn-out process has only exacerbated the despondency in the community. Will the Minister tell me when any new scheme will be implemented? The community of people affected need assurances that any improvements to the system will be introduced as soon as possible and sustained long beyond that. Will she commit to a debate in Government time to allow for appropriate scrutiny of the package? We should have a full day of discussions on the matter once the Government have responded to the consultation.

I am sure that the public health Minister appreciates that the longer this goes on, the longer we leave in place a system that does not work and leaves victims without adequate support. No amount of money will ever fully make up for what happened, but we owe to those still living with the consequences the dignity of a decent lasting settlement. It is time to act.