We polled our members on this question. Eighty per cent of them were in support of advance consent, for example, in cases of dementia.
I think this is fundamental to how we apply assisted dying legislation. Are we truly going to be patient-centred and give people what they want?
There was a time when doctors didn't even let their patients know they had a diagnosis of imminent death. I think we've really moved from that to a time of being patient centred.
My colleague suggested that she felt every patient's life had value, and I commend her for that, but really isn't it up to the patients themselves to decide whether they want to continue living in a state where they clearly don't? I think we can be very specific with the wording and the direction of advance consent, laying out particular criteria so we can tightly control it, but I think it is fundamental.