I am so conflicted over this.
My MIL is end stage dementia and has been in a care home for 7 years. She has muscle contracture for which she is heavily medicated, pretty much locked in a near foetal position. She stopped recognising anyone over 5 years ago. She is a tiny scrap of a thing. She had recently started having seizures for which she us now medicated. There are indicators she may have some form of bowel cancer. I have H&W POA and I have agreed with doctors that investigation of this would be too traumatic and so would any treatment. The emphasis on all sides is on comfort and dignity.
When we cared for her at home, and she still had awareness of her diagnosis she begged for help in ending her life, but of course, that was not an option. The emphasis on "living well" despite dementia was relentlessly pushed.
In her situation now, I'd happily - well, not happily - I'd be distraught - allow a cocktail of happy meds to give her a more peaceful end.
I would have done the same for my Mum when she spent the last three days of her life comatose due to ovarian cancer but was still instinctively responsive to pain.
But this is the thing. Assisted Dying can only be carried out when someone has capacity, so it will not help many with the dignified and pain free death they desire. Advance directives would not apply.
This safeguard is understandable to a degree.
And I also am concerned about mission creep given the current zeitgeist and attitudes to those who are deemed a drain in society.
In principal, I want the suffering to have their wishes respected. In practise, given experience I have had with the authorities in various situations, including healthcare, I am wary of legislation that can be amended with potential ulterior motives.
It is horrific to see someone slowly dying of anything, worrying about their pain, how aware they might be. I've done four such death beds, but these scenarios won't be addressed.
So overall, I'm hugely conflicted.