Assisted Dying Law

Rupa Huq Excerpts

Thursday 23rd January 2020 Westminster Hall

[Christine Jardine]

I thank the hon. Lady for that point. That is something we would have to be aware of, but I believe it is up to us to address it. It is up to the lawmakers and the Government in this country to ensure that we increase our investment in palliative care as a choice. There is that word again: choice. Free will—the ability to choose.

Seven years ago, in another landmark, my belief in that was firmed up by a conversation following a newspaper article I had written. At the time, the late, irrepressible Margo MacDonald was guiding her second, ultimately unsuccessful bid to make assisted dying legal in Scotland through the Parliament at Holyrood. I originally met Margo while I was a young journalist, and her amazing personality and commitment had a huge impact on me. That did not have an impact on my politics, of course—we had very different views—but I recognised in her someone who lived their beliefs and their politics. I had spoken to her while I was writing the piece, and I visited her office afterwards. On this issue more than any other, she had a profound effect on me. It was several years ago now, but that conversation has stayed with me and made me determined to protect the right of the individual—my right; your right—to choose to have the dignity that we want in our final moments. Why should any of us, knowing that we are not going to survive, be forced to endure unnecessary pain?

[Dr Rupa Huq (Ealing Central and Acton) (Lab)]

The hon. Lady is making a powerful speech. I am pleased that she has not brought any legislation before us, because I found this issue very difficult when we last faced it, in 2015. I actively abstained by voting in both Lobbies, and I was told off by the then Speaker for doing so. I get her point that saying goodbye in an airport is not the best thing for people who choose to go to Switzerland, but at the same time I worry about safeguards. This could be exploited as a shortcut if NHS funds are not as we want. Does she agree, at least, that more research is needed? Nothing seems to have happened in Parliament since 2015. We need more evidence before we decide on this.

[Christine Jardine]

I take the hon. Lady’s point. That is the purpose of this debate. It is intended to get the ball rolling, look for the evidence, find out what people are afraid of, and consider the safeguards we need and how the law can be improved. We are not going to do that overnight. We certainly are not going to do it today, and I will not suggest any changes today, other than to say that we should look for the evidence and at what people want from the law.

Since this debate was publicised, I have been contacted—I am sure we all have—by a number of constituents. In some cases, they called for caution; in others, they expressed their opposition. However, in very many more, they expressed support. One in particular that I found moving came from a woman who was a palliative care nurse for more than 20 years, and who during that time witnessed numerous examples of the current assisted dying law failing dying people. One example she gave was of a gentleman with motor neurone disease who had a particularly undignified final few months of life. He was cared for at home at first before moving into a hospice, where he clearly expressed the wish that he wanted help to die. The staff had to explain to him and go over the reasons why they could not do that; it simply was not possible.

This gentleman’s motor neurone disease had affected him in such a way that his legs were still working, but he was not able to use the top half of his body. One day, he tried to throw himself down the stairs as a way of ending his life. Despite him fully admitting that he was trying to end his life, some of the staff understandably claimed that he had probably fallen, and that it was an accident. Perhaps they did not want to admit or acknowledge what he had tried to do, because of the position in which the law put everyone, but that gentleman did not get to express his distress about the way he would die or have it addressed as he wanted. I understand he lived for another two months or so before he died in a hospice. I am grateful to my constituent for sharing that story because it highlights the invidious position in which the current law puts everyone.