Assisted Dying (No. 2) Bill Debate

Full Debate: Read Full Debate
Department: Ministry of Justice
Friday 11th September 2015

(8 years, 7 months ago)

Commons Chamber
Read Full debate Read Hansard Text Read Debate Ministerial Extracts
Chloe Smith Portrait Chloe Smith (Norwich North) (Con)
- Hansard - -

I think I speak for the whole House when I say that it is an honour to follow the highly personal statement by the hon. Member for Bridgend (Mrs Moon).

I am proud to take part in this debate. I, too, favour the Bill. We are thinking about what we would want for our loved ones or, indeed, for ourselves, although, professionally speaking, our personal views are not the prime focus of this debate. In part, I am speaking to express a few of my constituents’ views.

One constituent who is in favour of the Bill, said:

“I am a nurse and believe everyone has the right to die when they feel it is right for them”.

Another constituent spoke to me about his father’s death from a brain tumour. He said that his father was, in his words, “fogged by morphine”, and he wished that his father had been able to have a more meaningful time with the family. Other constituents have told me of their concerns about the measurement of terminal illness, the pressures in the NHS, the concept of utilitarianism and—as other hon. Members have mentioned—the respect accorded to palliative care. One constituent said:

“Please will you allow these real concerns to be heard in the debate?”

Our duty today is to listen well, think carefully, and clearly explain our decisions.

The current law is unclear and often people are forced to take hidden, undignified and desperate action. Some relatives and loved ones are risking criminal prosecution. Ethical problems exist today, whether for the patient, doctor or family—they are not invented by the Bill. We should aim to bring those dreadful ethical choices into the light, giving people dignity and support. We do not have to make carers risk a murder or manslaughter charge alongside their grief.

Most of all, I believe in a person’s right to determine their own life and the manner of ending it, as that is a sovereign principle. We each own our lives and no one else defines that for us. Indeed, that concept is already quite deep within the NHS when we speak of , “No decision about me without me”. I also want better palliative care, and I appreciated hearing the factual evidence provided by the National Council for Palliative Care. However, I have concerns about one ethical opinion that was implied among its facts. While explaining that doctors and nurses are

“ill-placed to make judgements on whether a request for assistance to end life prematurely stems from a clear and settled intent”

it stated that such matters are

“better decided by the courts.”

Those words forget the one person whose choice it really is—the patient. This is not about forcing someone, or indeed everyone, to do something; this is about ceasing to force an individual to do something that they no longer wish to do, which is to live.

Many make arguments about ethical issues and say that society is what matters, and I say that the human being is what matters most. The Church of England stated in its briefing for this debate that while an individual’s sense of personal worth is an “important consideration”, it

“cannot take the place of the intrinsic value of every person’s life.”

In other words, someone else gets to define the value of our life for us.

We all squeal when someone defines a person as worth less than we may think, but the more respectful and free response should be to resist defining a person in any way other than how that person wishes. We should trust people’s choices. This debate is not only about an individual’s wish to die but about the limits that ought to be placed on others, and the Church has been right to highlight that latter point. In my view, because the drugs in this Bill would only ever be self-administered, that aspect is controlled by what we are scrutinising today. Just as importantly, we should not be criminalising grieving families and friends. This right cannot mutate of its own accord. It is to give a small number of people who are suffering terribly, and their carers, the freedom not to suffer according to their stated wishes.

I cannot walk in everybody’s shoes—none of us can—but our job is to listen and to try to empathise and bring those points to the Chamber. The law must allow for different people’s positions. It is a matter of compassion, so let us have the courage to do that today.