I put maybe based in my own experience of seeing my parents go through terminal illnesses.
Dear God I am so sorry. All love to youRight now I am on Day 6 of sitting at my husbands bedside on Nil by Mouth waiting for him to die, what an ffing way to go, it is horrendous. The staff are wonderful doing everything they can to make him comfortable and out of pain and looking after me and now he doesn't move, speak or open his eyes and seems comatosed. He has Parkinsons, Lewy Body Dementia, Dysphagia, Pneumonia and Sepsis - how much more does he have to have for someone to put him out of his misery, it is grinding me down, I am not sleeping, depressed and upset but for goodness sake I am sure there should be a way out of this in a couple of days. I was told on day 1 he was going to die but it is dragging on which should not be able to happen.
Definitely don't disagree with your important points. Any law would have to be created with robust input from disability rights groups too. I totally get what those groups mean when they say no assisted dying without assisted living. I understand why people find it objectionable that society is debating assisted dying when so many aren't given the resources they need to assist them to live. I just find it wrong on a deep instinctive level that we can leave people to suffer unspeakably. Adults with capacity are given the autonomy to consent to or refuse treatments. That should extend to not prolonging a painful death too.I put no as you absolutely cannot prevent coercion and persuasion as human beings can’t help it. See what’s happening in Canada where people are subtly and not so subtly nudged to make this choice because the state won’t care for people adequately. It’s not surprising this is coming up now when there’s a large aging population we can’t support. It’s also very telling that conversations about assisted dying chosen freely by the individual very quickly turns to conversation about euthanasia chosen on someone else’s behalf. This is a very dangerous path to go down. People will definitely make the ‘choice’ to die rather than go into care and have to sell their home in order for children to inherit. This will almost certainly be encouraged within some families
I agree that the issue is more the trying to prolong life with interventions that’s an issue rather than actively putting people to sleepIt's usually the family rather than the patient objecting to a DNR even though Ethel is 92, blind, on a drip, suffering with no hope of improvement and her baby bird ribs would be smashed to bits with resus. We seem to have collectively forgotten that people do die. They don't last forever.
Even DNRs are a risk as it can be misunderstood to mean no medical intervention rather than just not resuscitating
My husband deals with a lot of DNRs (Cardiothoracic surgeon) for this exact reason. He has dealt with situations where the family doesn't know about the DNR, which is completely within the patients right, but had them yelling at him and threatening legal action if he doesn't resuscitate. I've luckily never been in the position of being the lead doctor on a case with a DNR but one has always stuck with me from med school regarding a child and a custody battle. Was absolutely heartbreaking.It's usually the family rather than the patient objecting to a DNR even though Ethel is 92, blind, on a drip, suffering with no hope of improvement and her baby bird ribs would be smashed to bits with resus. We seem to have collectively forgotten that people do die. They don't last forever.
So sorry for your lossWe put everything in place (POA) when he had the first signs of Parkinson's and there are copies everywhere they are needed.
But anyway I wanted to say that my husband passed away today and it was quite peaceful and so glad I was there holding his hand and talking to him when it happened, quite suddenly. It was something I wanted as it was cruel keeping him like that and sure he would have said the same as we have talked lots about it and he should not have been left for 7 days like this - not NHS fault as they have been faultless but something has to be done about this.
All my loveWe put everything in place (POA) when he had the first signs of Parkinson's and there are copies everywhere they are needed.
But anyway I wanted to say that my husband passed away today and it was quite peaceful and so glad I was there holding his hand and talking to him when it happened, quite suddenly. It was something I wanted as I think it is cruel keeping people in that state and sure he would have said the same as we have talked lots about it and he should not have been left for 7 days like this - not NHS fault as they have been faultless but something has to be done about this.
Much love to youWe put everything in place (POA) when he had the first signs of Parkinson's and there are copies everywhere they are needed.
But anyway I wanted to say that my husband passed away today and it was quite peaceful and so glad I was there holding his hand and talking to him when it happened, quite suddenly. It was something I wanted as I think it is cruel keeping people in that state and sure he would have said the same as we have talked lots about it and he should not have been left for 7 days like this - not NHS fault as they have been faultless but something has to be done about this.