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Elderly parents

Literally no one understands my reluctance to do personal care

358 replies

bringincrazyback · 25/09/2026 17:55

I just want to put that there for now, really, because this board has been just about the only place where people haven't made me feel like a strange/cruel person for saying that emergencies aside I want my DM's carers to handle her personal care (she lives with me) and I can only really get involved if it's needed at times outside of carer visits. Just been through it yet again with one of the carers this afternoon, and yet again I've been met with looks of incomprehension. It makes me feel so annoyed (especially as this never happens to men) but also ashamed that this is how petty and grudging I seem to be over some things. But feeling ashamed doesn't change the way I feel, unfortunately.

Is it reasonable for me to have this boundary (taking into account that I'd never leave my mum without personal care if she needed it), or do I just need to get over myself as a lot of people seem to think?

Sorry, just a quick vent for now as I need to see to DM now the carer's gone, but just needed to put this somewhere, just as a request for some empathy I guess, as I know some on here do understand it. (The only person who understands is DH, but of course if this ever happens to him with his mum he'll never be expected to do it anyway, being a man!) I'll add context later. Thanks for reading.

OP posts:
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AnnoyedAsAllHeck · 01/10/2026 09:22

ChimpanzeeThatMonkeyNews · 30/09/2026 07:04

Just ignore her. She clearly thinks she’s very clever, but her comments are witless.

With that poster, it's a case of "those who know the least, act like they know the most".

Rosscameasdoody · 30/09/2026 16:03

bringincrazyback · 30/09/2026 16:00

I'm sorry you and your mum went through that, it's such a cruel disease. I always think it's like a person with dementia dies twice - first the loss of who they are and then the physical death. 😕

That’s exactly it, thank you.

bringincrazyback · 30/09/2026 16:00

Rosscameasdoody · 30/09/2026 14:52

Agree. I think any kind of dementia is so hard. I watched my mum disappear right in front of me. Everything that she was had pretty much gone by the time she actually passed away. There were the odd flashes of my old mum but I’ll admit as she deteriorated they used to distress me because I couldn’t bear the thought of her being trapped in her body and aware of what was happening to her - thankfully the lucid periods were fleeting. I thought I’d done most of my grieving throughout her illness but it hit me like a brick when it finally happened. Six months down the line I can finally come to terms with the fact that her passing was the best thing for her. Anyone who has a loved one with this awful disease has my heartfelt sympathy.

Edited

I'm sorry you and your mum went through that, it's such a cruel disease. I always think it's like a person with dementia dies twice - first the loss of who they are and then the physical death. 😕

OP posts:
Rosscameasdoody · 30/09/2026 14:52

Kassiopea · 29/09/2026 19:01

We are lucky with our carers they go above and beyond. Apart from a select few we've been very lucky and they now feel part of our family almost. My mother is disabled now (for a reason nobody can find) so she cant look after my dad and he can't look after her. Doubly whammy. It's so hard with dementia, like a living grief.

Agree. I think any kind of dementia is so hard. I watched my mum disappear right in front of me. Everything that she was had pretty much gone by the time she actually passed away. There were the odd flashes of my old mum but I’ll admit as she deteriorated they used to distress me because I couldn’t bear the thought of her being trapped in her body and aware of what was happening to her - thankfully the lucid periods were fleeting. I thought I’d done most of my grieving throughout her illness but it hit me like a brick when it finally happened. Six months down the line I can finally come to terms with the fact that her passing was the best thing for her. Anyone who has a loved one with this awful disease has my heartfelt sympathy.

Rosscameasdoody · 30/09/2026 14:25

maxslice · 27/09/2026 22:20

You don’t know me. Stop pretending you do.

Based on what you’ve posted and the number of deletions I think we actually know you very well.

AvengingAngle · 30/09/2026 07:05

bringincrazyback · 29/09/2026 23:10

Glad the thread has helped. Posting it has helped remind me that those of us who are going through this are not freaks, we're people who are doing our best for those we love, but we're human and we simply can't always do everything our loved ones might require of us.

Totally agree, it is comforting to know that others are going through similar experiences and understand. I think it's something you can't fully understand unless you have actually been through it with your own parents or close relatives, but people who haven't had this experience can be either supportive or, sadly, judgemental.

ChimpanzeeThatMonkeyNews · 30/09/2026 07:04

Just ignore her. She clearly thinks she’s very clever, but her comments are witless.

thepariscrimefiles · 30/09/2026 07:01

This reply has been deleted

Message deleted by MNHQ. Here's a link to our Talk Guidelines.

WTAF! Who do you think you are to speak to OP like that and order her off her own thread? Your image of yourself as a compassionate saint is totally at odds with the reality if your many posts on this thread are anything to go by.

You owe OP an apology but I doubt that you have the awareness and the basic decency to do that.

bringincrazyback · 29/09/2026 23:15

Rosscameasdoody · 29/09/2026 18:34

Again this resonates OP. Mum was the same - and as the condition progressed there was a noticeable aversion to soap and water. Her dementia specialist nurse advised that some dementia sufferers can’t tolerate the feel of water on the skin - hairwashing for example, can be intolerable. The LA carers used it as a reason not to force her - they stated that if she had capacity they couldn’t insist. When I pointed out that in fact she didn’t have capacity they were less than pleased but it did improve the personal hygiene side of things once I’d made my point to the care agency providing the support. I have a disabled wet room with level access shower which was literally five steps from mum’s bedroom, so they really didn’t have a leg to stand on - not least because the private carer used to coax her gently into the shower and was a lot kinder once she was there !!

As far as anti depressants go you need to be really careful. Dementia is caused by underlying disease to the brain and many anti-depressants have the opposite effect to what they’re designed to do. I know this from horrible personal experience with mum. Ask about Mirtazipine. Unlike SSRI’s it can be given in small to moderate doses on an as and when needed basis, rather than at regular intervals, and it aids with sleep too.

Edited

That's helpful to read, she's meant to be starting sertraline but I'm nervous, as mentioned upthread. You've just reminded me that she used to be on mirtazapine and I can't remember why it was discontinued, but I think she tolerated it OK. Might be worth me asking the GP if restarting that is a better first step - thanks for mentioning it.

OP posts:
bringincrazyback · 29/09/2026 23:10

Rumtopfkirsch · 29/09/2026 22:40

I've been holding guilt about not being prepared to carry out personal care for my elderly parents who are no longer alive, if called upon at the time, for a couple of decades. Maybe it's simply a taboo for many of us. What a relief to hear I'm not a freak!

Glad the thread has helped. Posting it has helped remind me that those of us who are going through this are not freaks, we're people who are doing our best for those we love, but we're human and we simply can't always do everything our loved ones might require of us.

OP posts:
bringincrazyback · 29/09/2026 23:06

Kassiopea · 29/09/2026 18:23

Do you have power of attorney? You could talk to her GP about antidepressants?

In the process of applying for POA. She's actually meant to be starting on sertraline, but we keep having to hold off as she's had some physical health stuff going on and GP's advised we wait till things have settled. I have to say I'm nervous about sertraline as I've heard the side effects can make things worse rather than better in the short term, and I'm honestly not sure how she'd deal with even a temporary worsening, but I know we need to try something so am going to give it a shot when she's on a more even keel physically. I know she's going to need close monitoring though.

OP posts:
Rumtopfkirsch · 29/09/2026 22:40

I've been holding guilt about not being prepared to carry out personal care for my elderly parents who are no longer alive, if called upon at the time, for a couple of decades. Maybe it's simply a taboo for many of us. What a relief to hear I'm not a freak!

autumnisherenow · 29/09/2026 22:13

IDreamtOfManderley · 25/09/2026 18:28

sorry, typo mistakes above,she has accidents both bladder and bowel and she phoned me up and I’m expected to clear everything up

You have my sympathy. My mother is reasonably compos mentis but doesn’t like wearing pants. She had accidents from her rear end but doesn’t seem to notice. I make sure I always have shoes on indoors as I never know what my be lurking on the floor somewhere.

Kassiopea · 29/09/2026 19:01

Rosscameasdoody · 29/09/2026 18:39

Agree. We found this with mum. The morning carers got nowhere with her - not that they tried very hard, but later visits tended to be a bit more successful.

We are lucky with our carers they go above and beyond. Apart from a select few we've been very lucky and they now feel part of our family almost. My mother is disabled now (for a reason nobody can find) so she cant look after my dad and he can't look after her. Doubly whammy. It's so hard with dementia, like a living grief.

Rosscameasdoody · 29/09/2026 18:39

Kassiopea · 29/09/2026 10:32

It's true they lose their inhibitions. I don't know what stage you mum is at but my dad refuses to be washed in the morning. Most of our carers are the same ones that have been coming for 3 years now and are amazing and know my dad well. We find that my dad is easier to wash and agree to personal care later in the day. Most mornings it's just a no! One carer in particular will shower and shave him at the dinner time visit as he's quite happy then.

Agree. We found this with mum. The morning carers got nowhere with her - not that they tried very hard, but later visits tended to be a bit more successful.

Rosscameasdoody · 29/09/2026 18:34

bringincrazyback · 29/09/2026 13:20

My mum's moderate Alzheimer's on paper, but I think she's beginning to edge into severe, sadly. Many mornings the carers are greeted with 'I don't need a wash, I've just had one' which is almost never true. I can never quite tell if she really thinks she has (as once in a blue moon she actually will get up and wash unprompted before the carer arrives) or is just saying it because she doesn't want to wash (more likely). It's definitely not embarrassment, she's never been embarrassed about nudity, and in fact I often think part of my reticence to do personal care might stem from being laughed at by both my parents when younger about not wanting to see them with no clothes on or vice versa. 😔

Sadly her personal hygiene took a dive after my dad died, before she had even started with Alzheimer's, and she's needed prompting to wash and brush her teeth/hair ever since. I'm convinced she's depressed, and pretty deeply depressed at that, but it's very difficult to help with that because she categorically insists she isn't and won't hear of anything like counselling. 😔

Again this resonates OP. Mum was the same - and as the condition progressed there was a noticeable aversion to soap and water. Her dementia specialist nurse advised that some dementia sufferers can’t tolerate the feel of water on the skin - hairwashing for example, can be intolerable. The LA carers used it as a reason not to force her - they stated that if she had capacity they couldn’t insist. When I pointed out that in fact she didn’t have capacity they were less than pleased but it did improve the personal hygiene side of things once I’d made my point to the care agency providing the support. I have a disabled wet room with level access shower which was literally five steps from mum’s bedroom, so they really didn’t have a leg to stand on - not least because the private carer used to coax her gently into the shower and was a lot kinder once she was there !!

As far as anti depressants go you need to be really careful. Dementia is caused by underlying disease to the brain and many anti-depressants have the opposite effect to what they’re designed to do. I know this from horrible personal experience with mum. Ask about Mirtazipine. Unlike SSRI’s it can be given in small to moderate doses on an as and when needed basis, rather than at regular intervals, and it aids with sleep too.

Kassiopea · 29/09/2026 18:23

Do you have power of attorney? You could talk to her GP about antidepressants?

bringincrazyback · 29/09/2026 13:20

Kassiopea · 29/09/2026 10:32

It's true they lose their inhibitions. I don't know what stage you mum is at but my dad refuses to be washed in the morning. Most of our carers are the same ones that have been coming for 3 years now and are amazing and know my dad well. We find that my dad is easier to wash and agree to personal care later in the day. Most mornings it's just a no! One carer in particular will shower and shave him at the dinner time visit as he's quite happy then.

My mum's moderate Alzheimer's on paper, but I think she's beginning to edge into severe, sadly. Many mornings the carers are greeted with 'I don't need a wash, I've just had one' which is almost never true. I can never quite tell if she really thinks she has (as once in a blue moon she actually will get up and wash unprompted before the carer arrives) or is just saying it because she doesn't want to wash (more likely). It's definitely not embarrassment, she's never been embarrassed about nudity, and in fact I often think part of my reticence to do personal care might stem from being laughed at by both my parents when younger about not wanting to see them with no clothes on or vice versa. 😔

Sadly her personal hygiene took a dive after my dad died, before she had even started with Alzheimer's, and she's needed prompting to wash and brush her teeth/hair ever since. I'm convinced she's depressed, and pretty deeply depressed at that, but it's very difficult to help with that because she categorically insists she isn't and won't hear of anything like counselling. 😔

OP posts:
Kassiopea · 29/09/2026 10:32

bringincrazyback · 28/09/2026 18:29

My mum has Alzheimer's too. She has never been remotely bothered who does her personal care, so that's helpful in terms of her not minding paid carers doing it, but less helpful in that I don't think she understands why I would mind, ditto why I'd mind seeing her naked! She's mostly cooperative with the carers, but sometimes refuses a wash and I am quite concerned in case that becomes a pattern.

DH and I don't have children together, but I do have to say that if we did, I wouldn't dream of putting them through this. I think it's very much an expectation of previous generations and is hopefully dying out.

It's true they lose their inhibitions. I don't know what stage you mum is at but my dad refuses to be washed in the morning. Most of our carers are the same ones that have been coming for 3 years now and are amazing and know my dad well. We find that my dad is easier to wash and agree to personal care later in the day. Most mornings it's just a no! One carer in particular will shower and shave him at the dinner time visit as he's quite happy then.

ArcangelaTarabotti · 29/09/2026 08:12

rookiemere · 28/09/2026 21:35

@bringincrazybacksadly I don’t think it’s a generational thing, more of a dementia related issue. My pre dementia DM would have been horrified by what she expects of me, but the current one just sees me as human fixer.

Thankfully both DPs now in a care home near me and I never lived with them. She had carers through the council because we’re in Scotland and at one point one of them was muttering loudly about why DF (frail, 92 with dementia himself) wasn’t helping DM with her toileting, so I think some carers just very unhappy with the job - which I couldn’t do to be fair- and venting their frustration on those that they see as being more prosperous than they are.

I could literally do anyone else’s personal care in preference to my DPs, the whole thought of it repulses me, it’s such a strong sentiment and one I am not proud of.

I agree. Would do personal care for my partner but definitely not for my mother.

rookiemere · 28/09/2026 21:35

@bringincrazybacksadly I don’t think it’s a generational thing, more of a dementia related issue. My pre dementia DM would have been horrified by what she expects of me, but the current one just sees me as human fixer.

Thankfully both DPs now in a care home near me and I never lived with them. She had carers through the council because we’re in Scotland and at one point one of them was muttering loudly about why DF (frail, 92 with dementia himself) wasn’t helping DM with her toileting, so I think some carers just very unhappy with the job - which I couldn’t do to be fair- and venting their frustration on those that they see as being more prosperous than they are.

I could literally do anyone else’s personal care in preference to my DPs, the whole thought of it repulses me, it’s such a strong sentiment and one I am not proud of.

withoutwingsnow · 28/09/2026 19:47

Mil used to ask dh to leave the room when she got dressed for bed - and there wasn’t even a glimpse of briefs. He told me she recently berated him for not staying in the bathroom to help her and when he said he didn’t feel comfortable she said well you did it for your kids!

bringincrazyback · 28/09/2026 18:29

Kassiopea · 28/09/2026 10:50

My parents have carers. 100 percent agree with you on the personal care. Before we had carers in place i did do some personal care for them but i was not comfortable. Luckily my dad has Alzheimer's or he would have been absolutely mortified that i had to help him in the shower. I will do lots for them like shopping, cooking, cleaning.. but personal care is for their carers.

My mum has Alzheimer's too. She has never been remotely bothered who does her personal care, so that's helpful in terms of her not minding paid carers doing it, but less helpful in that I don't think she understands why I would mind, ditto why I'd mind seeing her naked! She's mostly cooperative with the carers, but sometimes refuses a wash and I am quite concerned in case that becomes a pattern.

DH and I don't have children together, but I do have to say that if we did, I wouldn't dream of putting them through this. I think it's very much an expectation of previous generations and is hopefully dying out.

OP posts:
Kassiopea · 28/09/2026 10:50

My parents have carers. 100 percent agree with you on the personal care. Before we had carers in place i did do some personal care for them but i was not comfortable. Luckily my dad has Alzheimer's or he would have been absolutely mortified that i had to help him in the shower. I will do lots for them like shopping, cooking, cleaning.. but personal care is for their carers.

Flamingpantoufles · 28/09/2026 10:25

Totally reasonable, OP. I had to do personal care for DM for a time and I really hated it & found it super stressful. I never want my DC to do this for me. And I agree that people never expect men to do this.

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