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Elderly parents

Watching my lovely mum slowly deteriorate from Alzheimer's is a really breaking me.

46 replies

Roselilysnowdrop · 24/10/2025 15:13

How the heck do you remain strong - year in, year out?

Seven years now of painfully witnessing my mum mentally and physically change from a beautiful lady who loved looking after herself, who never went out without make up on, clothing carefully co-ordinated with her jewellery/accessories to a little old lady who looks 10 years older than her actual 82 years old. Bent over and frail with osteoporosis, bright red eyes from glaucoma and cataracts, excessive hair on her face from the hormone blocking breast cancer medication and the now vacant stare of someone with advancing Alzheimer's. Someone who starts eats crayons like a 2 years old and sits staring at her hands like they are alien to her.

I see her most days and thankfully she often still knows my name but that's about it. She has a team of carers coming in throughout the day because she's now double incontinent following a fall in the summer and a month long hospital stay where the staff allowed her to constantly soil the bed. She went in continent and now has no bladder or bowel control.

You can not hold any conversation with my mum anymore (although I talk to her all the time as I'm convinced she understands me), she tries to talk but the words don't come out and that absolutely breaks my heart. How frustrating to be locked in your own body.

And that's my poor mum's life from now on.....carers wiping her bum, changing her pull ups and her daughters and husband doing everything else. Just sitting in her recliner day in and day out.

I know I'm very lucky to have had my mum in my life for all of my 52 years but if the truth be told I'd have much preferred her to have gone quick from a sudden hear attack like her own mother did at 76.

What kind of life is a life with advanced dementia? Bloody heartbreaking one for all involved, that's what it is.

Utter respect for anyone involved in dementia care and/or caring for loved ones. What a thoroughly wicked disease - it's a robbing bastard.

OP posts:
Sportsdaywinner · 24/10/2025 17:11

So sorry
It is an evil disease.

donteventhinkaboutthat · 24/10/2025 17:17

Awful disease. I saw something about people being in the advanced stages of dementia responding to singing/music. Accessing a different part of the memory?

Did she work outside the home?

ChaliceinWonderland · 24/10/2025 17:20

Roselilysnowdrop · 24/10/2025 15:13

How the heck do you remain strong - year in, year out?

Seven years now of painfully witnessing my mum mentally and physically change from a beautiful lady who loved looking after herself, who never went out without make up on, clothing carefully co-ordinated with her jewellery/accessories to a little old lady who looks 10 years older than her actual 82 years old. Bent over and frail with osteoporosis, bright red eyes from glaucoma and cataracts, excessive hair on her face from the hormone blocking breast cancer medication and the now vacant stare of someone with advancing Alzheimer's. Someone who starts eats crayons like a 2 years old and sits staring at her hands like they are alien to her.

I see her most days and thankfully she often still knows my name but that's about it. She has a team of carers coming in throughout the day because she's now double incontinent following a fall in the summer and a month long hospital stay where the staff allowed her to constantly soil the bed. She went in continent and now has no bladder or bowel control.

You can not hold any conversation with my mum anymore (although I talk to her all the time as I'm convinced she understands me), she tries to talk but the words don't come out and that absolutely breaks my heart. How frustrating to be locked in your own body.

And that's my poor mum's life from now on.....carers wiping her bum, changing her pull ups and her daughters and husband doing everything else. Just sitting in her recliner day in and day out.

I know I'm very lucky to have had my mum in my life for all of my 52 years but if the truth be told I'd have much preferred her to have gone quick from a sudden hear attack like her own mother did at 76.

What kind of life is a life with advanced dementia? Bloody heartbreaking one for all involved, that's what it is.

Utter respect for anyone involved in dementia care and/or caring for loved ones. What a thoroughly wicked disease - it's a robbing bastard.

So sorry. Sending hugs x

Perfectlypea · 24/10/2025 17:20

I’m so sorry OP - it’s absolutely heart breaking and I can’t imagine what it must feel like to lose your DM in such a devastating way…

I have a copy of the Alzheimer’s gene. I’m only early 50s but there’s not a day that goes by that it doesn’t hit me full force and absolutely terrify me. I don’t want my DC to have to nurse me.

PermanentTemporary · 24/10/2025 20:51

I’m so sorry. That’s a really heartfelt post and your love for her really shows.

Alphabetagammadelta · 24/10/2025 20:56

So sorry for you, I lost me beloved uncle to Alzheimer’s earlier in the year. He had a few years of coping at home then after a few falls, was in a care home latterly. It’s so hard seeing your elders look so frail. I found the care home visits hard going especially on my own. Do you have siblings and other close family to support you?

Karatema · 24/10/2025 21:36

I understand completely. My lovely MiL slowly deteriorated from a beautiful woman to a very old lady. Her bright, lively mind was gone and her sons mourned her loss long before she actually died.

Throwawayagain1234 · 24/10/2025 21:43

Hey OP, hugs, you sound like your mum is in a very similar place to mine. She was incredibly stylish too, known for her bright lipsticks and classy clothes. Now she is also doubly incontinent and recently didn't even understand the concept of me buying her a gift or the fact that it was a gorgeous cashmere cardigan for her to wear.

I wish for a giant brain bleed for her. Catastrophic and quick. The last three years have been impossible (since she really went downhill) and I struggle to comprehend how any of this is fair. My dad is fit as a fiddle but might as well not be as his life is stolen alongside hers. God it's just awful!

So so sorry this is your life too. I hope everyday you get a little gift of a happy moment to keep you going Flowers

Mrsmooja · 24/10/2025 22:48

Couldn't pass by without sending a virtual hug. In a similar situation with my mum xxx

tragichero · 24/10/2025 22:59

So sorry to hear this. We are going through the same with my lovely dad (though mercifully he is not usually incontinent, so we are luckier than you in that)

. He is cared for at home by my mom, who is heroic, with some help from me, though I always feel I should do much more.

He is very unwell currently with what seems to be a bladder infection . We have chosen to care for him at home (with HCPs coming in) as hospital would distress him so much, but it's very challenging. I am looking at my second night of likely no sleep, and feel like I am going a bit mad! Mercifully my brother is coming to relieve me tomorrow, as selfishly I think I will crack without a break.

Sorry, I wanted to reply to you OP and have ended up banging on about my own situation.

It's a horrific thing. I think in a way you can't look at the big picture of what you have lost, or you start to go mad! You just have to try to focus on what's in front of you in that moment, I think. And if possible try to enjoy any small moments of happiness, and the love you all still share.

Wishing you and your family and your lovely mom all the best. Xxx

Roselilysnowdrop · 25/10/2025 11:34

Alphabetagammadelta · 24/10/2025 20:56

So sorry for you, I lost me beloved uncle to Alzheimer’s earlier in the year. He had a few years of coping at home then after a few falls, was in a care home latterly. It’s so hard seeing your elders look so frail. I found the care home visits hard going especially on my own. Do you have siblings and other close family to support you?

I do have a younger sister but she isn't too much help tbh, she always leaves things to me to deal with.

OP posts:
Roselilysnowdrop · 25/10/2025 11:39

Throwawayagain1234 · 24/10/2025 21:43

Hey OP, hugs, you sound like your mum is in a very similar place to mine. She was incredibly stylish too, known for her bright lipsticks and classy clothes. Now she is also doubly incontinent and recently didn't even understand the concept of me buying her a gift or the fact that it was a gorgeous cashmere cardigan for her to wear.

I wish for a giant brain bleed for her. Catastrophic and quick. The last three years have been impossible (since she really went downhill) and I struggle to comprehend how any of this is fair. My dad is fit as a fiddle but might as well not be as his life is stolen alongside hers. God it's just awful!

So so sorry this is your life too. I hope everyday you get a little gift of a happy moment to keep you going Flowers

I wish for the same for my mum and hate myself for feeling that way but I totally understand what you are saying.

My dad is the same as yours, he's 84 and is in very good health but he always says he may as well have dementia because it has robbed him of his life too. That's so hard to deal with, isn't it?

I really feel for you x

OP posts:
Roselilysnowdrop · 25/10/2025 11:40

Mrsmooja · 24/10/2025 22:48

Couldn't pass by without sending a virtual hug. In a similar situation with my mum xxx

I am so sorry you are in the same boat, I really feel for you Flowers

OP posts:
Roselilysnowdrop · 25/10/2025 11:50

tragichero · 24/10/2025 22:59

So sorry to hear this. We are going through the same with my lovely dad (though mercifully he is not usually incontinent, so we are luckier than you in that)

. He is cared for at home by my mom, who is heroic, with some help from me, though I always feel I should do much more.

He is very unwell currently with what seems to be a bladder infection . We have chosen to care for him at home (with HCPs coming in) as hospital would distress him so much, but it's very challenging. I am looking at my second night of likely no sleep, and feel like I am going a bit mad! Mercifully my brother is coming to relieve me tomorrow, as selfishly I think I will crack without a break.

Sorry, I wanted to reply to you OP and have ended up banging on about my own situation.

It's a horrific thing. I think in a way you can't look at the big picture of what you have lost, or you start to go mad! You just have to try to focus on what's in front of you in that moment, I think. And if possible try to enjoy any small moments of happiness, and the love you all still share.

Wishing you and your family and your lovely mom all the best. Xxx

I'm sorry you are going through this too.

From our experience with mum being in hospital in the summer I would say you are doing the best thing, caring for your dad at home whilst he is unwell. Unless it is an absolute necessity we have made the decision that mum is not to be admitted to hospital. She went on to the ward fully continent but they allowed her to soil the bed every day, I suppose this was due to staff shortages and ease for them but it has cost us dearly (physically, emotionally and financially). I pleaded with them not to do this but it fell on deaf ears so we are left with mum now always double incontinent.

I hope everything goes well with your dad and he overcomes the infection quickly. It is such a worry when they become poorly, isn't it? They just can not fully communicate how they feel.

Wishing you all the best too xx

OP posts:
DPotter · 25/10/2025 12:23

Dementia really is the shittiest disease.

It's no wrong and is completely understandable you wish for a quicker death. This is not something to feel guilty about.

Someone mentioned music up thread and I strongly recommend playing your Mum's favorites. My Mum loved the classic musicals - Singing in the Rain, Carousel etc and she would become a bit more alert and sway a little.

At some point (and it sounds like you may not be far away) we shifted our care focus from Mum to my Dad, who was an absolute trooper but in the end he simply couldn't provide the care my Mum needed so the decision to place Mum in a care home was a combination of her needs and Dad's. And actually as difficult a decision as it was, it was the right thing to do. Mum did perk up for a while and was more active in the care home. And Dad flourished once he could get some decent sleep. Mum lived for another 2 years in the care home and was well cared for.

tragichero · 25/10/2025 14:29

Roselilysnowdrop · 25/10/2025 11:50

I'm sorry you are going through this too.

From our experience with mum being in hospital in the summer I would say you are doing the best thing, caring for your dad at home whilst he is unwell. Unless it is an absolute necessity we have made the decision that mum is not to be admitted to hospital. She went on to the ward fully continent but they allowed her to soil the bed every day, I suppose this was due to staff shortages and ease for them but it has cost us dearly (physically, emotionally and financially). I pleaded with them not to do this but it fell on deaf ears so we are left with mum now always double incontinent.

I hope everything goes well with your dad and he overcomes the infection quickly. It is such a worry when they become poorly, isn't it? They just can not fully communicate how they feel.

Wishing you all the best too xx

OP, I am so sorry that happened. I must say, faecal incontinence is one thing mom and I would really struggle to cope with I think, much as we love him. We can both cope with dealing with a bit of wee (he actually tries to get to the loo for both, but sometimes gets wee on himself, bless him) but double incontinence I think would be beyond our abilities - and would rob him if even more dignity, the poor man.....

It's awful that that happened to your mom, for her and for you .....

Do you have much support in RL? Friends who understand, a partner, counselling even?

I am lucky in that I have a good circle of friends, but I am thinking of seeking professional counselling too. I even ended up emailing an ex earlier, today whom I don't even like in many ways, but the one thing we shared was experience of dementia - and he was actually amazing with my dad, despite being less than great in many other ways..... But that has made me realise I am perhaps not coping as well as I like to think I am.....

Purplecatshopaholic · 25/10/2025 14:34

Been there, it’s shit. My mum hung on for way too many years, just disintegrating before our eyes mentally and physically. Didn’t know who we were, where she was, could do nothing for herself. The vibrant, intelligent, lovely person she was, was gone years before she actually died. Its a fucking awful, evil disease.

ladygindiva · 25/10/2025 21:17

Sending hugs. My dad has Alzheimer's and it's just so awful. He was the most intelligent person I've ever known and with a razor sharp wit and I miss him although he's still here, if you know what I mean. You're not alone x

StrongLikeMamma · 25/10/2025 22:28

Utterly heartbreaking. Sending huge hugs to you OP 💛

Choux · 25/10/2025 23:24

The mum I had 10 years ago would be horrified if she could see the person she has become now. She has been in a care home for 2.5 years but would have been in one longer if it wasn’t for my dad looking after her until he died. The home is lovely and the staff genuinely care about her but she is now starting to get distressed a lot. Especially screaming in the night. They can’t give her sleeping tablets as then she would be a falls risk and need someone to sit with her and they don’t have spare staff to do that so it appears the answer is going to be to move her at 93 to an Elderly Mentally Ill (EMI) unit with higher staff ratios and mental health nurses. I feel like she is now suffering more than living and yet there’s nothing I can do.

ByTwinklyDreamer · 25/10/2025 23:29

I am so sorry.

My DM is 74 and has Alzheimer’s, he hasn’t known who I am for over a year now, it’s such a cruel condition.

RememberDecember · 25/10/2025 23:37

I am so sorry. Also on this journey. Day by day I feel a little bit more of my mum.

ozarina · 25/10/2025 23:46

I can remember my Mum asking me Why is this happening? I've not been a bad person. It's awful. I sat there and wished I had the courage to smother her with a pillow. I'm so sorry. The good thing is she has you to look out for her. Many have no one.

AyrshireTryer · 25/10/2025 23:50

Firstly hugs, big hugs with tears and understanding.
My mom went quickly. She died at the start of Covid after going for her nursing home into hospital and back out again. Thanks Boris.

She went for her assessment at the Alzheimer's clinic and met a couple she hadn't seen for years, chatting about all the old times, but couldn't answer any of the doctor's questions. Although 'who is the current Prime Minister?' was a pretty difficult one at the time.

One of the last things she forgot was my name. My dad's and sister's names both lost weeks before. I had been premature and she had named me herself - as I was not the gender they were expecting, so perhaps that helped.

Stories came that I had never heard, lots of stories from her teenage years and early 20s. Great stories about boyfriends before and surprisingly during her courting of my dad. The little minx!

And tales of when we were young children and she had felt she hadn't been a good enough mother - we lived in a tower block and once she had managed to lock herself out on the balcony - chops under the grill and my sister 5 and me 1 in the flat. Saved by my dad coming home early and no doubt saving us all. She told me how she still dreamt of that.

We could only have 12 at the funeral, back in those Covid days. I remember having to wait for the gravestone as they had run out of the stone we wanted. The stonemason saying they had a lot of work on, which of course I understood.

OP I have no great advice for you. It is s**t. My mother died in layers, It is so cruel.
But OP lots and lots of hugs.

Dance the dance, eat the cake, buy the fcuking shoes.

CharlotteCChapel · 25/10/2025 23:50

I was lucky with DMiL as DD took over as primary carer, she's an experienced dementia carer. This meant she had someone qualified with her at all times. I supported her as a family member.

The end kind of rushes up on you. We started caring for DMiL in July, following DFiL's death. She was reasonably mobile with her zimmer and could go out into the garden. Then she would try to go downstairs from her bedroom but get stuck half way down. By November she'd live in a reduced area only going from her new downstairs bedroom (the dining room ) to the toilet and to the living room. She was in and out of hospital due to falls. In early December she fell out of bed and got stuck. The paramedics weren't happy with her condition and she was admitted to hospital where she started showing signs of a chest infection, we all had it, and died in hospital in early January.

The worst bit was after she died and there's that awful feeling of relief and sorrow mixed up.

I hope you wont take this wrong way but it seems like the end will be soon and her suffering will be over.

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