Assisted Suicide

John Healey Excerpts

Tuesday 27th March 2012 Commons Chamber

[John Healey (Wentworth and Dearne) (Lab)]

It is a pleasure to follow the hon. Member for Enfield, Southgate (Mr Burrowes), who I think led the Adjournment debate in January, about which he told the House, and spoke very clearly this afternoon.

I pay tribute to the Backbench Business Committee, because as far as I can see, notwithstanding the hon. Gentleman’s debate, this is the first substantive debate that we have had in the House, probably since the Suicide Act was passed in 1961.

We are asked to welcome the DPP’s policy for prosecutors on assisted suicide, and I do. I also strongly support the amendment in the name of the hon. Member for Congleton (Fiona Bruce), which stresses the importance of better palliative and hospice care, and we need to look at and go further with the law in this country, but the amendment in the name of my right hon. Friend the Member for Lewisham, Deptford (Dame Joan Ruddock) is, in my view, not necessary and not sufficient.

We are blessed in Rotherham with a superb hospice, 15 beds, day places and a community hospice team. The hospice is supported by a dedicated team of staff, by more than 330 volunteers and by residents throughout Rotherham, who raise more than £2 million a year to support its work, but no care, however good, can entirely relieve suffering at the end of life, and some will choose to hasten their own end and will require and request assistance in doing so from those closest to them. That is the subject of today’s debate, and of the DPP’s policy, which clarifies and does not change how the law is applied.

Before the policy, we did not know how the DPP used his discretion on whether to prosecute under the 1961 Act, but we do now, and I hope that this House will strongly endorse that policy, because it is compassionate and reasoned.

Thinking about this debate, I remembered Debbie Purdy, to whom tributes have been paid, and that it was the power of her personal arguments, as much as her legal arguments, that had such force. At the time, she said:

“I was preparing to lose and was in the middle of organising to go to Dignitas. Winning was like being given permission to be alive… I was reliant on somebody loving me enough to risk his liberty in order to support my choices. Now, I know I am not dependent on that”.

She reminds us that this issue is as much about living as dying, as much about independence as dependence and as much about the family as the person facing the decision on their own death. But above all it is about control over what is perhaps the ultimate act and decision, to end one’s own life, taken by people who are mentally competent to decide but physically incapable of acting to do so without assistance.

My concern, despite the policy, is that we are left in this country in a legal no-man’s land. For those looking to travel abroad to die, we have a policy of non-prosecution for compassionate assistance but a law that still makes it a criminal offence, and that law, in circumstances in which it exists but is not enforced, is flawed. In circumstances in which someone does not have the means to travel abroad to die, we are not just in no-man’s land legally; we have a clinical and ethical fudge.

Doctors do hasten the end of some patients’ lives in some circumstances, and they get around the prohibition on doing so through continuous sedatives, excessive sedatives, dehydration and starvation. Discussion on that treatment and care is often clouded in ambiguity, is disguised by the “Doctor knows best” attitude, is not open, is not honest and is not properly recorded.

We deprive those who need such assistance of being able to obtain it in this country; we deprive ourselves of the proper—sufficiently strong—safeguards against it being misused; and above all, because of the situation we are in, we deprive too many people of control and dignity in dying, and it is high time we changed that.