Josh Fenton-Glynn

I am sorry; I will not just now. This Bill has an auto-commencement clause, which means that within four years of the passage of this Bill—whatever the state of our health service, of our social care, or of our palliative care; even if there has been another pandemic—it will come into force. That brings me to our safeguards. I cannot vote for a Bill that does not sufficiently guard against coercion. That is what my constituents with disabilities say they fear the most and, having been in charge of social care, I know what that looks like. Let me be clear: the safeguards in this Bill are not enough. If the Bill in its current form passes, a patient would be subject to more scrutiny to give up a kidney than to give up their life. The ultimate weakness of this Bill is that the question being asked when a patient goes to the panel is a medical and legal one, not a social and psychological one. The main judgment will be an assessment of whether they are likely to die in the next six months, not of why they have chosen to die or whether there is a risk of coercion. Coercion is not always committed by the traditional villain; it is not someone who wants money. It is often committed by a loved one at the end of their tether, as support falls away, money drains, options narrow and people’s sense of what choices they have narrow, too. Without improving palliative care, we will put far too many people in that heartbreaking position. As MPs, we are used to being forthright in our opinions and advocating for ourselves and our constituents. On our Select Committee, we constantly hear from vulnerable patients who say that they are frequently ignored, talked about or talked over by medical professionals. They feel talked at, not talked to. When considering this legislation, I do not ask whether it will work for people like me; I ask whether it will work for the most vulnerable—those whose voices are rarely heard and who are most dependent on the state for protection. They rely on us to be their voice. The Bill comes from a place of compassion, but it could lead to a place where a disabled person feels that they are less. It could lead to a place where poor social care means that people do not feel that they have a choice between a comfortable life and an early death. That is why I say, with a heavy heart, not this Bill and not at this time.