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Elderly parents

How long does this hell go on for?

190 replies

UnitaBath · 19/08/2026 09:10

Mum was diagnosed with Alzheimer's 8 years ago but I had been pushing for a diagnosis at least 2 years previously, so I imagine it's been 10 years +

I have been helping my elderly parents navigate this world of theirs almost every day for the last 6 years. I have become their PA in all sense and purpose, the person who has to keep track of everything in their lives, keeping their plates spinning in the air. A role I took on out of love but had zero notion of what I was getting myself into.

Mum has a pacemaker due to a heart condition, three years ago she was diagnosed with breast cancer, last summer she had a nasty fall in the garden fracturing her neck. In A&E we were told the type of fracture she had would most likely kill her within a month. She survived and after a month long stay in hospital she came home, worse than before and now doubly incontinent. The state she was in upon discharge we genuinely expected her to die at home within weeks but she kept pushing on. This winter she had an infection of 'unknown origin' and after a 36 hour wait in A&E corridors (where my father picked up norovirus) she had another stay in hospital which saw her deteriorate further and upon discharge to home her GP prescribed anticipatory medication as she appeared to be coming to end of life. 7 months on she is still here - bless her.

This summer has been awful for mum, the heat has exhausted her and she spends most of her days just sitting in her recliner chair with her feet up, sleeping on/off all day (she has to have her feet up or her they will turn purple/black). She can not speak, just looks at us with glazed expressions, is double incontinent so has carers in 3 times a day which is costing her £800+ per week. Every now and then she becomes animated and will smile and say a few words but it's very sporadic now.

Honestly, what kind of life is this? I cry every day for my poor mum. I love her so dearly and want her to live forever but obviously not like this, this is no life for her, for my dad or for my sister and I. It is such a wicked disease. Why does my mum's poor diseased body and brain want to keep clinging on to life, it is no life at all.

OP posts:
tsmainsqueeze · 21/08/2026 14:05

I appreciate the argument that the home owner should pay their own care home fees but what really riles me is that often for many years before a care home is finally needed the government do not take into consideration the amount of blood sweat and tears family members put into the care of their relative , ending up on their knees with nothing left to give.
Often with nothing or very little money left over to make the awful situation just that little bit less awful knowing at least there is a little something to look forward to.
I completely agree that many elderly people are just kept going in a state of existence, absolutely horrific for all involved .
I am currently watching the slow demise of my remaining parent , i find it hard fitting their needs around my own busy life and i admit to finding it a chore.
I think it will be a relief for them and us when their time comes ,however i feel guilty saying this.

Mischance · 21/08/2026 14:13

tsmainsqueeze · 21/08/2026 13:53

I relate to this - when helping my grandads cousin who needed a care home i had a social worker call me ,we had never met or spoken before and she said to me 'can you not pay or is it that you don't want to pay' .
I was quite taken aback !

And this is why I resigned from social work. I had spent many years working hard to improve the lives of many disadvantaged people and then I found myself turned into a financial gatekeeper for the local authority - no thank you!

UnitaBath · 21/08/2026 15:16

Thank you all for your advice and input. I am sorry so many of you have been or are going through similar issues.

I really feel it's time for poor mum to go into a care home, as much as that breaks my heart but I want to go back to being my parent's child and visiting them to chat and have a little laugh, I don't want to be PA/Carer etc anymore.

This morning has been nothing short of awful. The only real break we get is on a Friday when mum goes to the day centre for 5 hours. They are brilliant with her, they pick her up and bring her back and keep her occupied all day.

All went pear shaped this morning though. I got a phone call from the day centre to say mum had thrown up everywhere in their car on the journey back to the day centre and when they got her out she then had severe diarrhoea. No one could get hold of dad (turned out he was down at the local recycling centre where there is no phone signal). They called me saying they were on there way back with her and could I be there. I have awful emetophobia so this was not music to my ears but obviously I had little choice. I went into a blind panic (I know, I'm 53 with 2 dc I should be over that by now!). So I quickly went over to their house and waited for the car. Bless the lovely carer, she had cleaned mum up and put her in new clothes, I couldn't stop apologising to her, it's not what you want to be dealing with at work even if you are a carer. I shall get her a bunch of flowers next week.

Mum is now sleeping and seems ok, her temperature is quite low (35.4) so we have put a blanket on her and will be keeping a check on that for a few hours. Urgh, there is never a dull day.

Dad had arrived back and so I left, when I got into the car that song by D'ream 'Things can Only Get Better' was blasting out on the radio - all I could think was, I bloody well hope so because I don't know how much longer I can put up with this. The last 4 years poor mum has had to deal with so many health issues, endless UTIs, diarrhoea which no one can find a cause for, infections, the neck fracture, the breast cancer and on it goes..........

OP posts:
UnitaBath · 21/08/2026 15:21

Hoppinggreen · 21/08/2026 13:33

I am so sorry OP, its really tough
I lost my Mum to Parkinsons a couple of years ago but she deteriorated very quickly in about 3 or 4 months and then died sudenly in bed in her sleep. She had carers in and was really starting to lose quality of life and interest in anything and I was dreading the future (she told me she was too)
While I grieved I was very glad she went when she did in the circumstances she did and I am so sorry you don't have the same peace

I am sorry for your loss but I understand what you are saying. I love my mum dearly and I hate myself for the words I am about to type but I do want her to go now and to go swiftly and as peacefully as possible. It's what we all want isn't it? For our loved ones and ourselves. Who would want to carry on like this? I know pro-life campaigners would have a differing opinion but you would have to be fairly hard-hearted to think this qualifies as life.

OP posts:
UnitaBath · 21/08/2026 15:23

tsmainsqueeze · 21/08/2026 14:05

I appreciate the argument that the home owner should pay their own care home fees but what really riles me is that often for many years before a care home is finally needed the government do not take into consideration the amount of blood sweat and tears family members put into the care of their relative , ending up on their knees with nothing left to give.
Often with nothing or very little money left over to make the awful situation just that little bit less awful knowing at least there is a little something to look forward to.
I completely agree that many elderly people are just kept going in a state of existence, absolutely horrific for all involved .
I am currently watching the slow demise of my remaining parent , i find it hard fitting their needs around my own busy life and i admit to finding it a chore.
I think it will be a relief for them and us when their time comes ,however i feel guilty saying this.

I totally agree with everything you are saying. It's seems so cruel all round and no one cares.

OP posts:
OhamIreally · 21/08/2026 22:08

UnitaBath · 19/08/2026 10:15

We changed GP surgeries for mum this year over to mine and they've been wonderful. We have a ReSPECT form in place with DNR and she is only to be taken to hospital for breakages and little else because hospital stays leave her worse rather than better.

We don't agree to any vaccinations now but that is a battle with dad because he feels they are essential. Everything is a battle with my dad sadly which makes a difficult situation much worse but that's a while other story.

This is a good point about vaccinations. I always said yes because my mum was very pro-vaccine but now I look back and think that was a mistake given the circumstances.

rookiemere · 22/08/2026 08:59

tsmainsqueeze · 21/08/2026 14:05

I appreciate the argument that the home owner should pay their own care home fees but what really riles me is that often for many years before a care home is finally needed the government do not take into consideration the amount of blood sweat and tears family members put into the care of their relative , ending up on their knees with nothing left to give.
Often with nothing or very little money left over to make the awful situation just that little bit less awful knowing at least there is a little something to look forward to.
I completely agree that many elderly people are just kept going in a state of existence, absolutely horrific for all involved .
I am currently watching the slow demise of my remaining parent , i find it hard fitting their needs around my own busy life and i admit to finding it a chore.
I think it will be a relief for them and us when their time comes ,however i feel guilty saying this.

One of the most extreme ironies to me is by the time DPs finally did end up in a care home, my entire life was decimated. I have gone from a professional well paid job to part time at a little bit over minimum wage. Unless there is anything left for me to inherit, I won’t have the funds to allow the choice of a care home when I want it, but will have to wait until the state deems I need one, effectively impacting DS in the future as well. Hopefully the recent stress means I won’t live so long.

Sortingmyself · 26/08/2026 09:58

@UnitaBath
How are you doing? How's things?

UnitaBath · 26/08/2026 13:46

Sortingmyself · 26/08/2026 09:58

@UnitaBath
How are you doing? How's things?

Thank you for asking.

We took mum to look around a local care home yesterday, I was taken aback at how lovely it was. We have been looking at a few over the last 6 months or so and none were any good and two made me weep, they were that bad but this one was completely different, it had a lovely feel to it. We are going to try to get mum in for 3 weeks respite when I have my op in October and if things go well then we will look into something more permanent in the new year.

The guilt feels overwhelming though, I had very much hoped that we’d never have to put mum in a care home.

OP posts:
Ilovemyfam · 26/08/2026 14:40

That guilt!!!!

Two hours ago I said goodbye to Mum in her care home. Mum is not happy but the home is good. Mum would not be happy if she was in the Ritz. She wants to be at home but is not safe.

I am glad you have found somewhere you like/can trust. Don’t forget to start the respite early enough to iron out any hiccups before you go to hospital. On a practical level, labels for clothes are important. My sister has a little machine and orders printed name tags. Mums home is small enough that the laundry are good at identifying what belongs to whom. Apparently her tall FIL was always wearing someone else’s trousers when they visited.

Know that you are not alone.

UnitaBath · 26/08/2026 16:52

Ilovemyfam · 26/08/2026 14:40

That guilt!!!!

Two hours ago I said goodbye to Mum in her care home. Mum is not happy but the home is good. Mum would not be happy if she was in the Ritz. She wants to be at home but is not safe.

I am glad you have found somewhere you like/can trust. Don’t forget to start the respite early enough to iron out any hiccups before you go to hospital. On a practical level, labels for clothes are important. My sister has a little machine and orders printed name tags. Mums home is small enough that the laundry are good at identifying what belongs to whom. Apparently her tall FIL was always wearing someone else’s trousers when they visited.

Know that you are not alone.

Thank you so much. It's means a lot, it's quite a lonely existence when all your friends have no idea of the hell which is an elderly parent with dementia.

The guilt really is something else isn't it? But I suppose we will feel that guilt whatever we do?

Thanks for the tip, I will have a look for a label machine.

OP posts:
Sortingmyself · 26/08/2026 17:24

UnitaBath · 26/08/2026 13:46

Thank you for asking.

We took mum to look around a local care home yesterday, I was taken aback at how lovely it was. We have been looking at a few over the last 6 months or so and none were any good and two made me weep, they were that bad but this one was completely different, it had a lovely feel to it. We are going to try to get mum in for 3 weeks respite when I have my op in October and if things go well then we will look into something more permanent in the new year.

The guilt feels overwhelming though, I had very much hoped that we’d never have to put mum in a care home.

I hear you...oh the guilt will be off the scale. I'm currently trying to speak to SS about putting DM into a care home for 2 weeks respite so DF can have a break. We've not told DM yet (she wouldn't even remember any conversations about it) so I'm parking the guilt until we have that discussion; not something I'm looking forward to as she was quite difficult when we last did it around 18 months ago. 😑I'm glad you've found somewhere suitable though and once she's in there, you'll see she's being cared for appropriately and you'll be able to bring your shoulders down away from your ears a bit hopefully!

Let us know how things go for you x

UnitaBath · 26/08/2026 18:59

Sortingmyself · 26/08/2026 17:24

I hear you...oh the guilt will be off the scale. I'm currently trying to speak to SS about putting DM into a care home for 2 weeks respite so DF can have a break. We've not told DM yet (she wouldn't even remember any conversations about it) so I'm parking the guilt until we have that discussion; not something I'm looking forward to as she was quite difficult when we last did it around 18 months ago. 😑I'm glad you've found somewhere suitable though and once she's in there, you'll see she's being cared for appropriately and you'll be able to bring your shoulders down away from your ears a bit hopefully!

Let us know how things go for you x

Thank you. I truly hope all goes well with the respite for your mum, it’s so difficult isn’t it but we all need that break now and then, we can only do so much. Good luck with it all Flowers

OP posts:
Ilovemyfam · 27/08/2026 18:02

UnitaBath · 26/08/2026 16:52

Thank you so much. It's means a lot, it's quite a lonely existence when all your friends have no idea of the hell which is an elderly parent with dementia.

The guilt really is something else isn't it? But I suppose we will feel that guilt whatever we do?

Thanks for the tip, I will have a look for a label machine.

I’ve tried to find a link to the name label machine. It might be micro stitch gun. Let me know if you want a link.

When Mum was in rehab one of the other patients was always giving away other patients clothes! It disturbed everyone. It was worth it.

MrsMoastyToasty · 27/08/2026 18:21

Several years ago my aunt and uncle went into a care home that had some double rooms. Aunt had dementia, uncle didn't. Have you considered finding something similar?

Hadalifeonce · 27/08/2026 21:01

We had to ask MiL's GP to stop prescribing antibiotics, all they did was stop the infection but prolong the suffering for a woman with no idea of anything, afraid of everything. It was heartbreaking.

UnitaBath · 28/08/2026 08:36

Ilovemyfam · 27/08/2026 18:02

I’ve tried to find a link to the name label machine. It might be micro stitch gun. Let me know if you want a link.

When Mum was in rehab one of the other patients was always giving away other patients clothes! It disturbed everyone. It was worth it.

That will be great, thank you.

OP posts:
UnitaBath · 28/08/2026 08:52

MrsMoastyToasty · 27/08/2026 18:21

Several years ago my aunt and uncle went into a care home that had some double rooms. Aunt had dementia, uncle didn't. Have you considered finding something similar?

My dad wouldn't be up for that, for an 85 year old he's actually in really quite good health and just wants to get out and about, I think the stress of caring for mum in their home is finally getting to him (and us all).

OP posts:
UnitaBath · 28/08/2026 08:54

Hadalifeonce · 27/08/2026 21:01

We had to ask MiL's GP to stop prescribing antibiotics, all they did was stop the infection but prolong the suffering for a woman with no idea of anything, afraid of everything. It was heartbreaking.

It really is such a heartbreaking disease. Mum had been on so many antibiotics over the last 18 months and they give her awful diarrhoea which is not only upsetting and uncomfortable for her but awful for the poor carers and us. We have stopped all medications like that. She is just on her breast cancer medication now.

OP posts:
katgab · 28/08/2026 09:03

UnitaBath · 26/08/2026 13:46

Thank you for asking.

We took mum to look around a local care home yesterday, I was taken aback at how lovely it was. We have been looking at a few over the last 6 months or so and none were any good and two made me weep, they were that bad but this one was completely different, it had a lovely feel to it. We are going to try to get mum in for 3 weeks respite when I have my op in October and if things go well then we will look into something more permanent in the new year.

The guilt feels overwhelming though, I had very much hoped that we’d never have to put mum in a care home.

It sounds like you’ve found a good place. Just like everything else they do vary. That said our care system is on its knees, leaving people and their families in a dreadful position. Honestly, I think we all feel guilt but, when it comes to this, there is no other option really and certainly no good ones.

It was an immense relief when my mum finally moved to a care home. The years before that had been awful in so many ways. It didn’t solve all the problems by any means but it relieved the pressure and allowed me to have some sort of life. It was a pretty decent home and the carers were many times better than any I could find for her at home. What she really wanted was something nobody could give her and that was to turn the clock back to when she had better health and could live independently.

It’s a horrible time for all and, once again, would like to offer some sense of support.

Ilovemyfam · 28/08/2026 09:11

katgab · 28/08/2026 09:03

It sounds like you’ve found a good place. Just like everything else they do vary. That said our care system is on its knees, leaving people and their families in a dreadful position. Honestly, I think we all feel guilt but, when it comes to this, there is no other option really and certainly no good ones.

It was an immense relief when my mum finally moved to a care home. The years before that had been awful in so many ways. It didn’t solve all the problems by any means but it relieved the pressure and allowed me to have some sort of life. It was a pretty decent home and the carers were many times better than any I could find for her at home. What she really wanted was something nobody could give her and that was to turn the clock back to when she had better health and could live independently.

It’s a horrible time for all and, once again, would like to offer some sense of support.

Agree about turning the clock back. Mum always says that she is fine at home. She talks about what she likes to cook etc. She is not fine in fact she is completely unsafe.

If she would accept her limitations and follow guidelines like staying in her chair when alone she could stay at home. She won’t so she can’t. Damn dementia.

IHopeTheNextSessionIsBetter · 28/08/2026 09:54

Hi OP
My heart really went out to you when I read your post. Mainly because I have been through it with my own parents and I know exactly what you are talking about. My case was slightly different because I gave up work to do it and so had more time than you. However my dad passed quickly after getting ill (within 8 weeks) so he was not too much bother really. My mum (diagnosed BPD) was the one that quite frankly just about killed me. My dad had done everything for her all his life including take her abuse once the kids left home. With him gone and my siblings refusing to get involved I became cook, cleaner, entertainment provider, admin sorter, scapegoat for her moods/abuse. I got seriously depressed and put on 6 stone. However I was dealing with a very difficult person who told lies regularly for attention (police, ambulance, siblings, friends). Then I would get a call from social services who were furious they had been called out in an emergency after my mum reported she had no food or money. They got to her house and of course she had both. Then they would phone me and I would get the flack for it (like I could control her?). I would take her to the doctors for antidepressants, she would cry noisely in the car park, the reception, the doctors office then after I had been to the pharmacy to get the tablets she would refuse to take them. She actually got a scan (MRI?) to check for dementia but she did not have it, just normal old person decline. This was less than a year before she died. I was getting paid to do this by the way by parent. I had honestly forgotten how bad she was having left home many years before and not seen the 'bad' side of her since I lived at home.
She changed her will to leave me her estate and told my siblings who promptly decided I had stolen her money so god knows what she told them. However she also left them a letter to tell them how disappointed she was in them which her solicitor passed after she died. I will no doubt be getting blamed for that as well by siblings even though I actually told her that was a really hurtful thing to do and the last thing she would ever say to them. Her response - I wish I could be a fly on the wall to see their faces when they realise they are getting nothing.

I haven't mentioned yet the scrubbing the shit stains out of the carpet when she became incontinent. Washing her soiled underwear. Doing personal care for her because she refused to let anyone else do it. Driving her to the chiropodist to get her nails cut as they got too tough for me to do where I had to talk her into letting the lady do it as she was black/brown and my mum wanted another chiropodist.

Ironically my siblings saved me (not on purpose) by pushing for her to go into a nursing home which she didn't want. She had a little bungalow on an old persons complex which was perfect for her and she wanted to die there. My siblings I think wanted her to go to care home so the inheritance was eaten up. She died 6 weeks after going in. Probably just as well as they were having a terrible time with her upsetting all the other residents and quite honestly she would not have got the same care she was getting from me. The relief when she died was overwhelming.

By this point she was on so many tablets which I religiously ensured she took every day although she used to talk about stopping them and then change her mind. I used to think how crazy it was keeping someone alive in this state but because she didn't have dementia and 'just' heart failure and then became frail and incontinent she was able to call ambulances every week and be taken to hospital where I think she enjoyed the attention.

For me the regular work of cleaning, appointments, admin etc was very busy and took over my whole world. I also had anticipatory grief dealing with her. A strange type of grief you have for a mother who was mentally ill/abusive but still grief and I would cry alot.

My dad needed help with admin, chores, appointments but he was cooperative and not abusive and even then I was pretty tired doing it for only 8 weeks.

I think it is a mixture of physical and mental exhaustion trying to remember everything that needs done, dealing with the grief of watching them decline, dealing with the effect on your own health, facing up to your own mortality as you think you are seeing your own future. I honestly didn't think I was going to survive it and honestly thought it was going to be 'me or her' ie if she didn't die soon, then I probably would.

In the end her heart gave out suddenly at the end in the care home but like I say strange how she suddenly died after I stopped looking after her. I still wonder if they accidently on purpose forgot to give her something as she was causing them so many problems.

Anyway almost 3 years later (I looked after her for four and a half years) I am only slowly recovering. Like you I didn't know what I was getting in to really. I didn't think it would go on so long and I had no clue as to how much work is involved in the looking after of an old person. So many appointments constantly. So much work trying to keep them clean, sane, entertained, happy. For my own ending I pray for a quick death - quick heart attack in my home and then gone. Not so good for whoever has to find me probably weeks later as I live alone but definately better for me.

We really do need to do something about keeping old people alive beyond when nature would have killed them off. Perhaps when they get to 80 or something medicine gets withdrawn and they are just kept comfortable. It's tricky though as I guess some older people live good quality lives on a few tablets and so withdrawing it for them would probably be wrong. Nobody wants to push the red button either so we are all got up in this trap of hell waiting for old person to die off.

I had a thread on mumsnet which helped me alot called so bloody exhausted waiting for old person to die started in Aug 2023. The thread took on a life on it's own and went on even beyond when my mum died as lots of people used the thread as comfort. There were versions 2 and 3 and I'm not sure how long it stayed alive for as I stopped reading it. Anyway it helped me alot to vent my frustrations and stay sane.
Only those that have gone through the exhaustion, the grief, the fear, the uncertainty, the constant limbo with no end date can understand.

I promise you it will pass but unfortunately you will never be the same person again. It will also take you a long time to recover from it all if you ever do.

Huge hugs.

SassyLemonFish · 28/08/2026 10:32

IHopeTheNextSessionIsBetter · 28/08/2026 09:54

Hi OP
My heart really went out to you when I read your post. Mainly because I have been through it with my own parents and I know exactly what you are talking about. My case was slightly different because I gave up work to do it and so had more time than you. However my dad passed quickly after getting ill (within 8 weeks) so he was not too much bother really. My mum (diagnosed BPD) was the one that quite frankly just about killed me. My dad had done everything for her all his life including take her abuse once the kids left home. With him gone and my siblings refusing to get involved I became cook, cleaner, entertainment provider, admin sorter, scapegoat for her moods/abuse. I got seriously depressed and put on 6 stone. However I was dealing with a very difficult person who told lies regularly for attention (police, ambulance, siblings, friends). Then I would get a call from social services who were furious they had been called out in an emergency after my mum reported she had no food or money. They got to her house and of course she had both. Then they would phone me and I would get the flack for it (like I could control her?). I would take her to the doctors for antidepressants, she would cry noisely in the car park, the reception, the doctors office then after I had been to the pharmacy to get the tablets she would refuse to take them. She actually got a scan (MRI?) to check for dementia but she did not have it, just normal old person decline. This was less than a year before she died. I was getting paid to do this by the way by parent. I had honestly forgotten how bad she was having left home many years before and not seen the 'bad' side of her since I lived at home.
She changed her will to leave me her estate and told my siblings who promptly decided I had stolen her money so god knows what she told them. However she also left them a letter to tell them how disappointed she was in them which her solicitor passed after she died. I will no doubt be getting blamed for that as well by siblings even though I actually told her that was a really hurtful thing to do and the last thing she would ever say to them. Her response - I wish I could be a fly on the wall to see their faces when they realise they are getting nothing.

I haven't mentioned yet the scrubbing the shit stains out of the carpet when she became incontinent. Washing her soiled underwear. Doing personal care for her because she refused to let anyone else do it. Driving her to the chiropodist to get her nails cut as they got too tough for me to do where I had to talk her into letting the lady do it as she was black/brown and my mum wanted another chiropodist.

Ironically my siblings saved me (not on purpose) by pushing for her to go into a nursing home which she didn't want. She had a little bungalow on an old persons complex which was perfect for her and she wanted to die there. My siblings I think wanted her to go to care home so the inheritance was eaten up. She died 6 weeks after going in. Probably just as well as they were having a terrible time with her upsetting all the other residents and quite honestly she would not have got the same care she was getting from me. The relief when she died was overwhelming.

By this point she was on so many tablets which I religiously ensured she took every day although she used to talk about stopping them and then change her mind. I used to think how crazy it was keeping someone alive in this state but because she didn't have dementia and 'just' heart failure and then became frail and incontinent she was able to call ambulances every week and be taken to hospital where I think she enjoyed the attention.

For me the regular work of cleaning, appointments, admin etc was very busy and took over my whole world. I also had anticipatory grief dealing with her. A strange type of grief you have for a mother who was mentally ill/abusive but still grief and I would cry alot.

My dad needed help with admin, chores, appointments but he was cooperative and not abusive and even then I was pretty tired doing it for only 8 weeks.

I think it is a mixture of physical and mental exhaustion trying to remember everything that needs done, dealing with the grief of watching them decline, dealing with the effect on your own health, facing up to your own mortality as you think you are seeing your own future. I honestly didn't think I was going to survive it and honestly thought it was going to be 'me or her' ie if she didn't die soon, then I probably would.

In the end her heart gave out suddenly at the end in the care home but like I say strange how she suddenly died after I stopped looking after her. I still wonder if they accidently on purpose forgot to give her something as she was causing them so many problems.

Anyway almost 3 years later (I looked after her for four and a half years) I am only slowly recovering. Like you I didn't know what I was getting in to really. I didn't think it would go on so long and I had no clue as to how much work is involved in the looking after of an old person. So many appointments constantly. So much work trying to keep them clean, sane, entertained, happy. For my own ending I pray for a quick death - quick heart attack in my home and then gone. Not so good for whoever has to find me probably weeks later as I live alone but definately better for me.

We really do need to do something about keeping old people alive beyond when nature would have killed them off. Perhaps when they get to 80 or something medicine gets withdrawn and they are just kept comfortable. It's tricky though as I guess some older people live good quality lives on a few tablets and so withdrawing it for them would probably be wrong. Nobody wants to push the red button either so we are all got up in this trap of hell waiting for old person to die off.

I had a thread on mumsnet which helped me alot called so bloody exhausted waiting for old person to die started in Aug 2023. The thread took on a life on it's own and went on even beyond when my mum died as lots of people used the thread as comfort. There were versions 2 and 3 and I'm not sure how long it stayed alive for as I stopped reading it. Anyway it helped me alot to vent my frustrations and stay sane.
Only those that have gone through the exhaustion, the grief, the fear, the uncertainty, the constant limbo with no end date can understand.

I promise you it will pass but unfortunately you will never be the same person again. It will also take you a long time to recover from it all if you ever do.

Huge hugs.

I remember those threads! Your opening message on the first thread was one of the most brilliantly poignant I have ever read on this forum.

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