Meet the Other Phone. Child-safe in minutes.

Meet the Other Phone.
Child-safe in minutes.

Buy now

Please or to access all these features

AIBU?

Share your dilemmas and get honest opinions from other Mumsnetters.

To think that we need to have an honest conversation about euthanasia and care costs

722 replies

Noras · 18/08/2024 17:41

So there are some interesting stats published by the Gov about the cost of cares the end of life and whatever way you look at it, it’s expensive. Obviously the most expensive is hospital care at about £400 to £500 per day but also care in care homes is high.Most of that could be avoided with an injection.

I have watched both my parents die and I have been left traumatised by it. My mother died from starving to death due to dementia in a non nursing bed with no pay relief other than paracetamol. She was clutching the sheets and morning for 14 days. My father died of the most gruesome cancer. We nursed him at home but we still had one 24 hour carer at the end paid for by CHC ( he was plus 2 for eg the commode and washing hence we still did it).

Whilst my parents were dying I could not bear to let them go but now after several years I think ‘What on Earth was that?’ With the benefit of hindsight I regret every mouthful of food that I fed my mother. She did not even know who I was and was in a different World but yet she was my beautiful mother.

I regret every time that I carefully measured morphine for my dad because I did not want to give him an overdose

I am haunted by the prospect of getting dementia. I am scared sick of cancer and dying from it as the pain meds never kept uo with the pain. When we just had the pain patches they were always too weak and we were always behind the race to keep up with the pain. When we got the end of life kit, as a relative I was always too scared to give ( I think ) enough morphine to top up the pain patches so my dad would he in agony. I could not bear to let my dad go - it was so painful,

So this is the question; Do we need to grow up and really think about euthanasia?

Over two years of my life were consumed by the impending death of my parents ( I still visited and cared for my mum in a care home despite it costing my dad several hundred pounds weekly as I wanted to care for her).

OP posts:
Thread gallery
13
Bumpitybumper · 19/08/2024 09:35

flapjackfairy · 19/08/2024 09:26

Well if people cannot advocate for themselves what qualifies you to say whether their life is worth anything or not ? Euthanasia for someone who can ask.for it and understand it is one thing but allowing babies, disabled children and adults to be killed ( because that is what would have to happen if they didn't die on demand to suit your agenda ) because they are an economic inconvenience is appalling .
And as others have pointed out why are we preserving the lives of prisoners and serial offenders then ? Should we start to.save the cost of housing these people ? Not to mention the rehabilitation and other costs involved in the penal system. Think how much money could be saved there.

See where does it end ? And people think.it is an overreaction to say it but that is the Nazi ideology of Hitler and Co.
He didn't just kill Jews for economic reasons but in the end anyone who didn't look sufficiently Germanic was fair game . So people were gassed for having large noses and looking a bit Jewish etc . And of course disabled were as well because anyone that wasn't perfect and didn't fit his agenda was in the firing line. And a whole nation went along with it ! People say it couldn't happen again but I only have to read a post like yours to see how it v easily could.

So that is why we talk about the slippery.slope! As soon as you decide one group of peoples lives are more important than another you are on v dodgy ground.

No, I disagree with you.

We are not 'killing' premature babies/very disabled people/very sick people by not offering every single life saving intervention to keep them alive. Most people could have their life extended if they received optimal healthcare and yet very few are afforded this due to financial and resource constraints. It isn't unique to vulnerable groups but it stands to reason that they may need more intensive healthcare earlier on in their lives and questions about cost (not just financial cost) and benefit are raised earlier on.

Hitler and prisoners are irrelevant. We need to be able to have a sensible discussion without automatically mentioning the Holocaust every 5 as seconds or banging on about financial savings that could be made elsewhere. We need to be able to have focussed, nature discussion on this specific issue resorting to irrelevances.

Supersimkin7 · 19/08/2024 09:37

Finance is relevant, but as a separate discussion.

Flopsythebunny · 19/08/2024 09:45

Plantparent · 18/08/2024 23:31

I doubt they did, morphine and controlled drugs are strictly counted and measured x

Really? The label on my oramorph says I can take it as and when I need it. The slow release zomorph is twice per day.

Starlingexpress · 19/08/2024 09:52

Flopsythebunny · 19/08/2024 09:45

Really? The label on my oramorph says I can take it as and when I need it. The slow release zomorph is twice per day.

You can self administer your morphine.

Administering drugs to somebody else is a whole other procedural process.

Starlingexpress · 19/08/2024 09:54

Bumpitybumper · 19/08/2024 09:35

No, I disagree with you.

We are not 'killing' premature babies/very disabled people/very sick people by not offering every single life saving intervention to keep them alive. Most people could have their life extended if they received optimal healthcare and yet very few are afforded this due to financial and resource constraints. It isn't unique to vulnerable groups but it stands to reason that they may need more intensive healthcare earlier on in their lives and questions about cost (not just financial cost) and benefit are raised earlier on.

Hitler and prisoners are irrelevant. We need to be able to have a sensible discussion without automatically mentioning the Holocaust every 5 as seconds or banging on about financial savings that could be made elsewhere. We need to be able to have focussed, nature discussion on this specific issue resorting to irrelevances.

So can you list the specific topics that are allowed in this discussion?

If vulnerable people and financial issues are off the table and irrelevant, what are we allowed to discuss?

Flopsythebunny · 19/08/2024 09:56

Noras · 19/08/2024 08:45

My father had 2 bouts of cancer before he died. After both significant operations, given the location of the melanoma, he wax released to my home to convalesce as I was at home due to SEN son. After the second more extensive surgery that went as far as his optic nerve, he had a haemorrhage all over my spare room, spare room bathroom and everywhere. it took an hour for an ambulance to appear and they rushed up the stairs with resuscitation equipment. That’s why I should I have been taught to pack the wound.

After he was terminal he was insistent on dying at home. I begged him to consider a care home or hospice but he refused. He was on funded care via CHC but he still refused. He felt that care homes and hospices were terrible places. Also he felt that he could conquer it, By now he had names and personified the cancer and referred to it getting excited in sunlight, My lovely brothers shared shifts with me because CHC care was just 3 short visits at bizarre times eg breakfast at 6 and lunch at 11. I would do the am shift until 2 and then fetch my son but inevitably it all went wrong. My brother would call because dad had fallen, could I get there. Once he let himself out on the driveway, collapsed and some neighbors kids were traumatised alerted their parent who got him back in. My oldest brother simply struggled with anything other than keeping him company etc. He was not able to mop blood etc. He was better used to fetch the pain control from some out of hours chemist miles away after we managed to get hospice of a GP out to agree to increase pain patches etc. My other brother did the late evening shift. however we all rotated as required and we all needed time off .As things progressed the care intensified and changed in nature from taking dad for a coffee and prayers in the church next door and a short walk to being in a wheel chair etc. As the carers turned up at 6am they left him in bed with congealed breakfast cereal. So I had the job to wash him all over and get him dressed. when I cleaned his personal areas I joked and said ‘clean your bits and pieces yourself dad’. At the early stage there were therapists sent in eg even OT and a whole load of equipment to try to stop falls before he lost mobility. So we did his exercises. Until 2 months before he died we also tried to get him out in a wheel chair to places eg the Zoo, Museums etc I carried the relief morphine in my handbag. We would call everywhere to facilitate him getting out and about easier. There is a lot of administration dealing with the care agency ( begging them for better hours visits) the CHC people, hospice, oncologists etc. Also radiotherapy still continued when terminal in an attempt to shrink the tumour in the back that was breaking his back bone, Getting dad out was overall challenging and was a plus 2 but we wanted him to get out a bit. Through all this period we were always chasing the pain, So we ended up frantically trying to get hospice on a weekend to get the next lot of pain patches. also the pain patches come off when being washed sometimes by care agencies - not me, Things were also so traumatic thst my DH insisted I going into the house first when dropping me off to check the state of things ( at that stage we were not doing overnight cover), We seemed to have been running around all the time. CHC are a pain in the arse as they insisted on a full meeting in December to assess needs when obviously needs were high , By now dad was unable to sit and slipped sideways, At this point agency care was put in but it was understood that they could not do transfers so if dad wanted to continue to use a commode we had to facilitate that etc. Also we had to allow the 1:1 time off etc. So I was still going in as did my brothers as she could not cope alone. The agency also could not cover all shifts, Over the Chrismas week we had to cover so the gaps. Brother covered dad from 7 to 1 on Christmas dad, we brought him to our home from 1 to 8 and then other brother stayed overnight, DH got up at 6 am Boxing Day to cover as brother had to go to work etc. Even when the agency worker was there we often got calls eg your dad is haemorrhaging etc. CHC brought in a live in carer but again that was in the understanding that dad was plus 2 for transfers and also that we needed to give her time off etc. At least we did not have all the issues with shifts being covered by the agency. After Christmas it became a blur. for some reason the live in carer was replaced with an agency but they were completely different - I think a nurse as they seemed really professional. We had a lady snd then a guy ( who was able to manage dad on the commode himself). By this stage, my dad looked like a complete horror show with visible blood coming from his orifices at all times. My dad still insisted on ambulating to toilet even though he was using a catheter for urine, There were issues with catheters and his urethra was blocked etc. In February I saw him and sat with him as he was curled in a ball in pain. He no longer engaged with me. I then went to see a consultant who finally told me that my son was ASD ( along with all the other issues he has). We came back to dad and I sat in the bed with him. I left him at 8 pm to get back to my daughter and son. At 9 pm we got the call to say that he had insisted on using the commode. He had died after sitting in it, his heart gave up.

Insofar as my mother was concerned my dad had been her primary carer as I was living in another city. My DH got offered partnership in a prestigious law firm ( top 20) but we were going to be too far away from my parents and luckily a firm in my parents city offered him partnership. I realised thst I needed to be near mum. Unbeknown to me my mother had been suffering a series of TIA and had severe heart failure. Dad had never managed to get her diagnosed with anything. I staged a sit in at the GP to get her diagnosed. That GP was later suspended for failure to show proper care to elderly with conditions like heart failure. He gave my mother antibiotics for her chesty cough! Thst was quite sick as can be seen. One day I get told that mum was having a funny turn, I went around and could see that mum was weakened on one side but dad refused to call an ambulance and said it would pass. I called my brothers and we had to literally beg dad to get 999 support. At that point we get told that mum had terminal heart failure as well as dementia. We brought mum home. at the time my sister was also helping so we split shifts with more people. My mum began to scream about pains in her legs at 1 am etc. She would not eat and slumped into her food. An ambulance was called. She was in hospital for several weeks and they stabilised her food intake by giving her sodium valproate. I was told by the specialist registrar that the mistake we made was calling the ambulance. We could not cope any longer so we placed her in a home. however dad was distraught and wanted her to eat. I was really still relatively young at the time with really young children one of whom was still having lengthy convulsions and his own issues. My dad wanted me to come to the care home with him to try to get mum to eat. I went hun every day to see mum for the next 7 months as he wanted me there.

We stupidly had placed her in a care home bed and it was not a nursing home, we did this because it was all new, sumptuous with an en suite and cost a lot at the time. On balance I regret that but we had been assured thst all her needs would be met. As the months went by, the efficacy of the sodium valproate wore off, mum could not eat or wanted to eat. She was starving to death. I begged dad to move mum to a nursing home but he refused. He accused me of making things difficult for him etc. The care home only gave my mother paracetamol as she thrashed and clutched at the sheets. They told the GP that they did not perceive pain. She was bringing her knees up to her stomach and grimacing. The week before she died she suffered blood loss from her bottom and shock. I think thst someone had tried to induce a poo using their fingers. The advice was to keep her situ. We had another week of intermittent calm and then the tossing and clutching at sheets with sickness. The GP did give her an antiemeretic. After she died, the care home manager left that care home. 2 weeks before my mother died I made the decisions with my dad not to use a feeding tube. After my mother died I found out that all the times I had looked after mum to give dad time off and put my son into nursery that I paid for to have the privilege of caring for mum, he had been seeing a mistress of 37 years.

This sounds very distressing for you, but surely even you can see that your dad caused all this? He refused to get a diagnosis for your mum, then refused her appropriate care.
When it came to his own illness, he refused appropriate care for himself.

Bumpitybumper · 19/08/2024 09:59

Starlingexpress · 19/08/2024 09:54

So can you list the specific topics that are allowed in this discussion?

If vulnerable people and financial issues are off the table and irrelevant, what are we allowed to discuss?

I haven't said vulnerable people and financial issues are off the table. This is literally what the discussion is about.

I simply suggested that Hitler and the Holocaust can't always be constantly referenced if we want to have a productive conversation about this topic. We also can't keep reasoning that because we have wasted public money on PPE, Rwanda, prisons etc that there simply must be an infinite supply of money to fund optimal healthcare for everyone. It is unrealistic and just acts as a distraction.

midgetastic · 19/08/2024 10:16

Money is artificial
It's a human concept originally designed to provide a type of exchangeable IOU for a service or goods

A society that can't afford to care for its elderly and dying isn't a society at all

MorrisZapp · 19/08/2024 10:22

midgetastic · 19/08/2024 10:16

Money is artificial
It's a human concept originally designed to provide a type of exchangeable IOU for a service or goods

A society that can't afford to care for its elderly and dying isn't a society at all

What should we pay care home staff with? Thoughts and prayers?

SerendipityJane · 19/08/2024 10:26

Shame the title wasn't "to think that we need to have an honest conversation about euthanasia and human dignity and suffering"

Rather sets a different agenda.

Still I guess if money is that important to some people.

flapjackfairy · 19/08/2024 10:31

Bumpitybumper · 19/08/2024 09:35

No, I disagree with you.

We are not 'killing' premature babies/very disabled people/very sick people by not offering every single life saving intervention to keep them alive. Most people could have their life extended if they received optimal healthcare and yet very few are afforded this due to financial and resource constraints. It isn't unique to vulnerable groups but it stands to reason that they may need more intensive healthcare earlier on in their lives and questions about cost (not just financial cost) and benefit are raised earlier on.

Hitler and prisoners are irrelevant. We need to be able to have a sensible discussion without automatically mentioning the Holocaust every 5 as seconds or banging on about financial savings that could be made elsewhere. We need to be able to have focussed, nature discussion on this specific issue resorting to irrelevances.

you absolutely did say that if people could not advocate for themselves then the decision should be made to end their lives. That is the part of your post I took umbrage with. .And as far as I can see no one is mentioning the holocaust every five minutes. In fact I was reluctant to add it into.my argument because people think.it is irrelevant and could never happen today.
Well just look at Canada for a start. It all starts off with noble lofty ideals but the goal posts are already being moved. The homeless and mentally ill are being given leaflets about euthanasia already and I was reading yesterday of a man who went into hospital and was left with a severe bed sore as he was left on a bed for 4 days without proper care . He was told it would be hard to heal and he was.then offered euthanasia . He took it as he was the kind of person who worried about being a nuisance . I would link.to it but I don't know how. It is being investigated at the moment.
Anyway that is the slippery slope in action and the alarm bells are already sounding loud and clear .

Medjoolfiend54321 · 19/08/2024 10:32

My mother and I have often talked about the idea of a life "with no point". She's in her mid-nineties, physically limited by age-related ailments. I have a very restricted, isolated life due to a chronic health condition. Both of us are in states we would, when younger, have deemed "not worth living". Both of us are happy. We had underestimated human adaptability, and overestimated the importance of vitality.

I think this is such a vital point. The decisions we make from within a mindset of youth and vitality can be so different when we find those things gone!

Two examples:

An elderly relative of mine was bed bound but still very much enjoyed life and enjoyed food. She was cared for by family and a rota of nurses some of whom didn’t seem to understand that for her, this was enough quality of life.

A friend of the family in his thirties had a form of cancer where the prognosis was not good and he made a series of advance decisions based on how he thought he would feel when certain capacities were gone. It turned out, when he reached that point, that he had very much changed his mind and very much wanted to live, despite not having the independence he thought he couldn’t live without.

Bumpitybumper · 19/08/2024 10:32

SerendipityJane · 19/08/2024 10:26

Shame the title wasn't "to think that we need to have an honest conversation about euthanasia and human dignity and suffering"

Rather sets a different agenda.

Still I guess if money is that important to some people.

But money is probably one of the main causes of human suffering in the world. Think how much pain could be stopped and lives saved if money was distributed differently. To pretend that it's somehow irrelevant to this discussion in bonkers.

If you had a set budget (which lets face it everyone, even the NHS does) how would you spend it to alleviate suffering and retain dignity? There isn't an easy or simple answer. It is fair and right to question enormous spending on a few when so many are in need.

TempestTost · 19/08/2024 10:32

Inlaw · 19/08/2024 01:45

Yes that was tough. I worked in one at the time. The residents who made it were never the same after. Many cried daily that this was worse than the war. Atleast then they had freedom they would say.

I can't understand how it was allowed. These were not people with no mental capacity for the most part. You cannot, or should not, be allowed to put an adult in a facility and tell them they are never allowed to leave. That's not a care home it's a prison, it's forcible confinement.

These organizations, or perhaps the government who made recommendations, ought to have been used. But these elderly don't have the time, energy, or money to spend on that.

COVID for me made it clear that I would never want to allow one of my parents to go into a care facility.

TempestTost · 19/08/2024 10:51

Lancrelady80 · 19/08/2024 03:04

First, people saying we should consider euthanasia prem babies can fuck right off, then fuck off some more. Noone knows what path they will take. Dd8 was born very early, unexpectedly, and came out blue. Cue incubator, then CPAP, then oxygen 24/7 for 9 months, tubefeeding, then when she was eventually allowed home (on her due date, still on oxygen, remaining so for months) she was repeatedly hospitalised with bronchiolitis. Looking at her now, she is no different to any other 8 year old and in fact far less of a fragile little waif then most of her peers. Functioning in every way absolutely as a typical 8 year old with zero back history.

Same message to those discussing young children with SEN...DS11 was clearly very badly delayed from a few weeks old. We have had SO much intervention and support from so many services. The paed told us clearly at 2, when still unable to sit, roll, babble, stand etc that they had absolutely no idea whether he would ever be able to do those things. He is now the oldest in his mainstream school, having delayed his start by one year, and other than dyspraxia, a slight issue with some sound pronunciation, and ASD traits, is functioning as any other child in his class.

Except in very sad and specific circumstances, noone knows how littlies will progress or what they will go on to achieve. That's before we even get onto medical breakthroughs, gene therapy etc.

We need to completely separate those issues from euthanasia and assisted dying. I actually think it should come to be allowed but with incredibly stringent criteria - and SEN or prematurity should be nowhere near the list! But it's terrifying reading how some would like it to be. This for example:

" First opportunity 40 (maybe), repeat after 10 years, again after 5 years times 3, and then offered the chance to update annually after that."

What a massive, massive form of insidious coercion and pressuring! By the age of 65, you have been asked five times if you want to be euthanized (in certain situations) and then asked again annually. So by 80, you have now had to consider your demise twenty times - surely that's going to make you feel like you should say yes, and that it's the right thing to do, and also now maybe people will stop hassling you about it.

The more I read the thread, the more I agree with an early poster who said something along the lines of she agrees in principle but doesn't think we can be trusted.

Two things - there is a reasonable question with babies in general around, not euthanasia, but what interventions to go ahead with. So, not intervening to prevent death when that would be the natural result of certain problems.

It's often a judgement call even with adults what interventions do more harm rather than help, but so much trickier with babies. But the more interventions there are, the more we need to think about when to stop them. At certain point it can become kind of a violation of the body.

However, what I would say about euthanasia, or even assisted suicide, with the elderly is it will inevitably impact on the kinds of situations you mean. It's because it changes and legitimizes the idea that some lives are too painful to lead.

You can see how this has progressed in some countries that started with the principle that adults who are in full control of mental faculties should be able to choose when there is no hope. The underlying assumption there is that there are lives too painful or sad to live.

But you very quickly see people begin to say - well then, what about people who no longer have faculties? DO we leave them in such a life? Don't we have a duty of care to them? What about people in a life like that, but death is not immanent? Isn't that even worse?

In some countries what you see is a drip drip of removal of safeguards in the legislation. In others, once you admit that there is a "right" to end life, the courts begin to say that restricting this is illegal/non-constitutional. In all of them these groups "advocating" for more and more people to have access to assisted death seem to emerge to take it to the courts and lobby political representatives. In Canada, an advisory group of doctors said that assisted death should be expanded to include infants - because that ignores our duty of care to them.

People seem to think this kind of approach will remain a last resort thing that people are careful about, but once it becomes normative, that can change. There have been plenty of societies that did not support their elderly when resources were scarce - and this was seen as moral and good. We aren't;t immune to that kind of idea, once we open the door to it.

TempestTost · 19/08/2024 10:59

Noras · 19/08/2024 08:45

My father had 2 bouts of cancer before he died. After both significant operations, given the location of the melanoma, he wax released to my home to convalesce as I was at home due to SEN son. After the second more extensive surgery that went as far as his optic nerve, he had a haemorrhage all over my spare room, spare room bathroom and everywhere. it took an hour for an ambulance to appear and they rushed up the stairs with resuscitation equipment. That’s why I should I have been taught to pack the wound.

After he was terminal he was insistent on dying at home. I begged him to consider a care home or hospice but he refused. He was on funded care via CHC but he still refused. He felt that care homes and hospices were terrible places. Also he felt that he could conquer it, By now he had names and personified the cancer and referred to it getting excited in sunlight, My lovely brothers shared shifts with me because CHC care was just 3 short visits at bizarre times eg breakfast at 6 and lunch at 11. I would do the am shift until 2 and then fetch my son but inevitably it all went wrong. My brother would call because dad had fallen, could I get there. Once he let himself out on the driveway, collapsed and some neighbors kids were traumatised alerted their parent who got him back in. My oldest brother simply struggled with anything other than keeping him company etc. He was not able to mop blood etc. He was better used to fetch the pain control from some out of hours chemist miles away after we managed to get hospice of a GP out to agree to increase pain patches etc. My other brother did the late evening shift. however we all rotated as required and we all needed time off .As things progressed the care intensified and changed in nature from taking dad for a coffee and prayers in the church next door and a short walk to being in a wheel chair etc. As the carers turned up at 6am they left him in bed with congealed breakfast cereal. So I had the job to wash him all over and get him dressed. when I cleaned his personal areas I joked and said ‘clean your bits and pieces yourself dad’. At the early stage there were therapists sent in eg even OT and a whole load of equipment to try to stop falls before he lost mobility. So we did his exercises. Until 2 months before he died we also tried to get him out in a wheel chair to places eg the Zoo, Museums etc I carried the relief morphine in my handbag. We would call everywhere to facilitate him getting out and about easier. There is a lot of administration dealing with the care agency ( begging them for better hours visits) the CHC people, hospice, oncologists etc. Also radiotherapy still continued when terminal in an attempt to shrink the tumour in the back that was breaking his back bone, Getting dad out was overall challenging and was a plus 2 but we wanted him to get out a bit. Through all this period we were always chasing the pain, So we ended up frantically trying to get hospice on a weekend to get the next lot of pain patches. also the pain patches come off when being washed sometimes by care agencies - not me, Things were also so traumatic thst my DH insisted I going into the house first when dropping me off to check the state of things ( at that stage we were not doing overnight cover), We seemed to have been running around all the time. CHC are a pain in the arse as they insisted on a full meeting in December to assess needs when obviously needs were high , By now dad was unable to sit and slipped sideways, At this point agency care was put in but it was understood that they could not do transfers so if dad wanted to continue to use a commode we had to facilitate that etc. Also we had to allow the 1:1 time off etc. So I was still going in as did my brothers as she could not cope alone. The agency also could not cover all shifts, Over the Chrismas week we had to cover so the gaps. Brother covered dad from 7 to 1 on Christmas dad, we brought him to our home from 1 to 8 and then other brother stayed overnight, DH got up at 6 am Boxing Day to cover as brother had to go to work etc. Even when the agency worker was there we often got calls eg your dad is haemorrhaging etc. CHC brought in a live in carer but again that was in the understanding that dad was plus 2 for transfers and also that we needed to give her time off etc. At least we did not have all the issues with shifts being covered by the agency. After Christmas it became a blur. for some reason the live in carer was replaced with an agency but they were completely different - I think a nurse as they seemed really professional. We had a lady snd then a guy ( who was able to manage dad on the commode himself). By this stage, my dad looked like a complete horror show with visible blood coming from his orifices at all times. My dad still insisted on ambulating to toilet even though he was using a catheter for urine, There were issues with catheters and his urethra was blocked etc. In February I saw him and sat with him as he was curled in a ball in pain. He no longer engaged with me. I then went to see a consultant who finally told me that my son was ASD ( along with all the other issues he has). We came back to dad and I sat in the bed with him. I left him at 8 pm to get back to my daughter and son. At 9 pm we got the call to say that he had insisted on using the commode. He had died after sitting in it, his heart gave up.

Insofar as my mother was concerned my dad had been her primary carer as I was living in another city. My DH got offered partnership in a prestigious law firm ( top 20) but we were going to be too far away from my parents and luckily a firm in my parents city offered him partnership. I realised thst I needed to be near mum. Unbeknown to me my mother had been suffering a series of TIA and had severe heart failure. Dad had never managed to get her diagnosed with anything. I staged a sit in at the GP to get her diagnosed. That GP was later suspended for failure to show proper care to elderly with conditions like heart failure. He gave my mother antibiotics for her chesty cough! Thst was quite sick as can be seen. One day I get told that mum was having a funny turn, I went around and could see that mum was weakened on one side but dad refused to call an ambulance and said it would pass. I called my brothers and we had to literally beg dad to get 999 support. At that point we get told that mum had terminal heart failure as well as dementia. We brought mum home. at the time my sister was also helping so we split shifts with more people. My mum began to scream about pains in her legs at 1 am etc. She would not eat and slumped into her food. An ambulance was called. She was in hospital for several weeks and they stabilised her food intake by giving her sodium valproate. I was told by the specialist registrar that the mistake we made was calling the ambulance. We could not cope any longer so we placed her in a home. however dad was distraught and wanted her to eat. I was really still relatively young at the time with really young children one of whom was still having lengthy convulsions and his own issues. My dad wanted me to come to the care home with him to try to get mum to eat. I went hun every day to see mum for the next 7 months as he wanted me there.

We stupidly had placed her in a care home bed and it was not a nursing home, we did this because it was all new, sumptuous with an en suite and cost a lot at the time. On balance I regret that but we had been assured thst all her needs would be met. As the months went by, the efficacy of the sodium valproate wore off, mum could not eat or wanted to eat. She was starving to death. I begged dad to move mum to a nursing home but he refused. He accused me of making things difficult for him etc. The care home only gave my mother paracetamol as she thrashed and clutched at the sheets. They told the GP that they did not perceive pain. She was bringing her knees up to her stomach and grimacing. The week before she died she suffered blood loss from her bottom and shock. I think thst someone had tried to induce a poo using their fingers. The advice was to keep her situ. We had another week of intermittent calm and then the tossing and clutching at sheets with sickness. The GP did give her an antiemeretic. After she died, the care home manager left that care home. 2 weeks before my mother died I made the decisions with my dad not to use a feeding tube. After my mother died I found out that all the times I had looked after mum to give dad time off and put my son into nursery that I paid for to have the privilege of caring for mum, he had been seeing a mistress of 37 years.

I think you have misplaced your anger here op. It sounds like your father's care was terribly managed. There were all kinds of places where decisions could have been made not to resuscitate, not to do a surgery.

Who was pushing/advising these things? If your father, that was up to him though maybe someone needed to tell him what the outcomes would really be. If the doctors, they were failing in their job.

But there should have been no need for euthanasia.

IncessantNameChanger · 19/08/2024 11:10

TempestTost · 19/08/2024 10:51

Two things - there is a reasonable question with babies in general around, not euthanasia, but what interventions to go ahead with. So, not intervening to prevent death when that would be the natural result of certain problems.

It's often a judgement call even with adults what interventions do more harm rather than help, but so much trickier with babies. But the more interventions there are, the more we need to think about when to stop them. At certain point it can become kind of a violation of the body.

However, what I would say about euthanasia, or even assisted suicide, with the elderly is it will inevitably impact on the kinds of situations you mean. It's because it changes and legitimizes the idea that some lives are too painful to lead.

You can see how this has progressed in some countries that started with the principle that adults who are in full control of mental faculties should be able to choose when there is no hope. The underlying assumption there is that there are lives too painful or sad to live.

But you very quickly see people begin to say - well then, what about people who no longer have faculties? DO we leave them in such a life? Don't we have a duty of care to them? What about people in a life like that, but death is not immanent? Isn't that even worse?

In some countries what you see is a drip drip of removal of safeguards in the legislation. In others, once you admit that there is a "right" to end life, the courts begin to say that restricting this is illegal/non-constitutional. In all of them these groups "advocating" for more and more people to have access to assisted death seem to emerge to take it to the courts and lobby political representatives. In Canada, an advisory group of doctors said that assisted death should be expanded to include infants - because that ignores our duty of care to them.

People seem to think this kind of approach will remain a last resort thing that people are careful about, but once it becomes normative, that can change. There have been plenty of societies that did not support their elderly when resources were scarce - and this was seen as moral and good. We aren't;t immune to that kind of idea, once we open the door to it.

With regards to babies where do you draw your line? I had pre eclampsia so the natural thing would have for me to die still pregnant. That's,nature and possibly good for evolution as its survival of the fitness.

If I cut myself and bled out that's nature's,way.

If I had an infection that's nature's way.

If my teen got stabbed that's nature's,way to bleed out. But these are totally different situations. If your 15 and get stabbed you could be saved, then go and live a long productive life. If you have dementia you will never recover. You eill never get better. You could make a pre directive in your poa to make your own choices. The ill and young wouldn't and couldn't choose this.

Slso as a mum of three kids,with SEN two of them aren't like any mainstream peers. One will never be so. He is severely disabled so can he get popped off? Just keep the ones who turn out OK in mainstream?

We was talking about end of life with the OP. For elderly terminal people. If your 80 and have dementia or terminal cancer getting better is never an option. Dementia is basically your organ failure from old age in the majority of cases.

ObelixtheGaul · 19/08/2024 11:30

IncessantNameChanger · 19/08/2024 11:10

With regards to babies where do you draw your line? I had pre eclampsia so the natural thing would have for me to die still pregnant. That's,nature and possibly good for evolution as its survival of the fitness.

If I cut myself and bled out that's nature's,way.

If I had an infection that's nature's way.

If my teen got stabbed that's nature's,way to bleed out. But these are totally different situations. If your 15 and get stabbed you could be saved, then go and live a long productive life. If you have dementia you will never recover. You eill never get better. You could make a pre directive in your poa to make your own choices. The ill and young wouldn't and couldn't choose this.

Slso as a mum of three kids,with SEN two of them aren't like any mainstream peers. One will never be so. He is severely disabled so can he get popped off? Just keep the ones who turn out OK in mainstream?

We was talking about end of life with the OP. For elderly terminal people. If your 80 and have dementia or terminal cancer getting better is never an option. Dementia is basically your organ failure from old age in the majority of cases.

Agreed, but the point being made is that the one can lead to the other. It's all very well to say 'keep it to these boundaries', but it's a door that has been opened. And if you open a door just the tiniest crack, someone will want to open it a crack more. And someone else will say, 'OK, if we are doing this already, it's not unreasonable to do that.'. And a few years down the line, we have a post on Mumsnet saying, 'it's time to have an honest conversation about...'
The very fact that some people on this thread have mentioned some other things they think should be considered tells us what that door opens.
It isn't reasonable or fair to keep the door of ending suffering through dementia closed because of that, but I understand why it creates a stumbling block.

Starlingexpress · 19/08/2024 11:31

‘We was talking about end of life with the OP. For elderly terminal people’

And that is how the conversation started in Canada.

Shutting down debate by insisting that this is about elderly terminally ill people shows a real lack of acknowledgement of what is happening in Canada and how people who are far from elderly and/or terminally ill are being impacted.

YellowAsteroid · 19/08/2024 11:31

All of you happily advocating for euthanasia for the old - I guess you're all quite young & inexperienced? Come back with more measured thoughts when you're 60.

YellowAsteroid · 19/08/2024 11:32

Starlingexpress · 19/08/2024 11:31

‘We was talking about end of life with the OP. For elderly terminal people’

And that is how the conversation started in Canada.

Shutting down debate by insisting that this is about elderly terminally ill people shows a real lack of acknowledgement of what is happening in Canada and how people who are far from elderly and/or terminally ill are being impacted.

Indeed, @Starlingexpress There are some very distressing & scary stories coming out of Canada - women with depression being "gently" pressured into euthanasia, for example.

MorrisZapp · 19/08/2024 11:34

YellowAsteroid · 19/08/2024 11:31

All of you happily advocating for euthanasia for the old - I guess you're all quite young & inexperienced? Come back with more measured thoughts when you're 60.

I don't want euthanasia to be for anyone other than myself, should that need arise. I don't want other people of any age euthanised without their express, clear and multiply witnessed personal demand.

Gettingbysomehow · 19/08/2024 11:35

I've been qualified as a nurse for 45 years and I am absolutely furious that I have no say in how I want to end my life. I absolutely do not want to end up in a care home. I want euthanasia when I want it.
It's so backwards that we can give our pets a wonderful death to end suffering but not ourselves and the reasons against it are just not good enough.
I'm still working so I'm busy saving up the 20k plus it will cost me to go to Dignitas. but lots of people cannot afford that.
I have a do not resuscitate plan in place already but that isn't enough in my opinion.

Prenelope · 19/08/2024 11:37

I'd be quite happy in a care home as long as I could look around me and listen to books. It certainly wouldn't be deal breaker.

Gettingbysomehow · 19/08/2024 11:37

YellowAsteroid · 19/08/2024 11:31

All of you happily advocating for euthanasia for the old - I guess you're all quite young & inexperienced? Come back with more measured thoughts when you're 60.

Actually I'm 62 and have witnessed hundreds of deaths during my NHS career, as a result I'll fight for euthanasia until my last breath.