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Am I right to regret ever sleep walking into becoming my partners carer?

308 replies

RakshaUK · 11/10/2025 20:17

It started with getting up in the early hours to help him put his socks on to go to work. Then he developed leg ulcers, so showers became a performance because the dressing on the ulcers couldn't get wet, so I had to help putting a waterproof sleeve over them.
Then, about 15 years ago he started to develop a lump in his groin, GP thought it was a lipoma, said it could be removed when it became a problem. About 5 years ago - 2020 it was limiting his mobility to such an extent he couldn't walk from his disabled parking space to his desk (they did look at moving his desk under reasonable adjustments but it wasn't thought to be reasonable because they IT dept needed to be able to communicate easily). So the week before we went into lockdown, he took early retirement!
Basically he sat in his chair all day, wouldn't do anything else, and complained that he was losing his mobility. I pointed out on an almost daily basis that if he didn't use it, he'd lose it. GP sent a lovely chap to try and motivate him, he'd agree to all the tasks, then not do anything about them.
He's been referred to 3 different surgeons with regard to the removal of the lump (which is now so big it hangs like a good sized pumpkin between his knees), one took a look at his belly, which hangs infront of it after losing about 5 stone, and declared it was a pannus not a lipoma!
We've since moved and our current surgery are trying to get a MultiDisciplinaryTeammeeting together, including him, and me to act as his advocate, since July! He's spent 4 weeks in hospital with cellulitis.
What is really getting to me is his attitude towards me. E seems to do as little as possible and leaves me to clear up after him.I'm not one of nature's nurses, I feel like a caged animal listening to his moans and cries, and of course he must feel worse...
So WHY WONT HE DO ANYTHING ABOUT IT?
Even his nurses say he's got to be a squeaky wheel and on the phone to the GP Surgery every day. He does nothing to help himself, or me. I'm 65, older than him, with my own mobility issues (I use a power chair outside if I have to), I'm also type 2 diabetic and recently diagnosed ADHD and Autistic. I also have many incidents of trauma in my life which haven't all been put to bed. His nurse today suggested he make me a cup of tea every day (I have a shower stool out there to sit on when I'm cooking or washing up that he could use) doing that would double his step count for the day!
He passes wind, and doesn't apologise. He leaves shitty finger prints every where (he will go to the toilet for poos, but doesn't wash his hands) Wees he has to do by standing up while I shove a washing up bowl underneath him (the lump means he sprays wee everywhere and dribbles if he's anywhere near wanting to go when he walks) He can't wear underwear or incontinence pads because of the lump, trousers are a thing of the past, so he has a blanket across his knees to hide everything.
I like our house, i like sharing it with my two dogs and two cats. I have just had it up to here with being his carer.

OP posts:
RakshaUK · 12/10/2025 05:26

HauntedBungalow · 11/10/2025 23:32

Why isn't the NHS treating this man? Who are these nurses going on about squeaky wheels? Why aren't they getting him treatment?

Nobody wants to take on the responsibility.
The District Nurses come to dress his leg ulcers every week. They advised him to be the squeaky wheel because it's the one that gets oiled. Ie the more of a nuisance you make of yourself the more likely you are to get treated.

OP posts:
Duckswaddle · 12/10/2025 05:22

Christ, you’re a better woman than I am.

RakshaUK · 12/10/2025 05:22

Bluecrystal2 · 12/10/2025 04:49

Absolutely disgusting and there's no excuse for his filthy habits. I would insist on him going to a care facility and if he ever goes into hospital I would refuse to have him back home. How horrible, you've done enough for him.

I've tried refusing to have him back, they put carers in 'because it's his home too' Even they couldn't get him to take a shower. Rarely was it the same two, even rarer could they speak English, or follow my instructions regarding the dogs. It sent my Autism into overdrive having these people in my house 😞

OP posts:
RakshaUK · 12/10/2025 05:17

SpaceCat3000 · 12/10/2025 04:27

Hi there,
I’m a little younger than you but in a similar situation. Both myself and my husband are disabled in different ways, and both have alot on our plates in our own ways. We both essentially care for each other, either one picking up the lions share for things the other really struggles with or simply cannot do. We’ve got it down to a fine art thesedays and when something new comes along (we jokingly say “oh well, just add it to the list of issues”) like a new medical problem on either side, we figure out who can do what, and do our best with it.

Now, my marriage is not perfect. I’m currently in a sexless marriage bevause hubbys pain and mobility issues really do a number on his libido etc, and while I also have 23/7 dreadful pain and mobility issues, I still have a high sex drive and would love any sort of sexual touch (doesn’t have to be sex, just close sensual touch etc). Alas, this is not to be and I’ve accepted that, I think.

Ive drifted from my point. What I’m trying to say is that while we both suffer with separate but quite rare disabilities, and we both have horrible relentless pain, we both do our absolute best for each other and for ourselves. I’m due for another round of physio? I’ll probably moan about it a bit, but give it my all and push through the pain with the guidance of my husband right by my side. Hubby needs another infusion which leaves him totally drained for weeks? He will moan about it but he will be there early for the appointment come hell or high water, and rest where he can for those weeks thereafter. What I’m trying to say is that we both get up, wash up and show up, for each other, for ourselves, for our kids etc. It sounds like your husband has let go of all dignity, and this is very sad indeed. For some years after my diagnosis, I would only wash when I could smell my own body odour, which I’m very ashamed to say.

I feel that from your post, you are being taken for granted and your husband had forgotten how important it is to get up, smarten up and show up for you, for himself, and for getting into the right frame of mind. You are wonderful for what you are doing.

I suggest a gentle talk. Ensure he knows that you find it an honour to care for him, and that you know he didn’t ask for this illness to happen. But it’s important to gently remind him that carers suffer from burnout, even carers who are wives. If he won’t do a thing to help himself, it’s making your job so much harder. If you burn out, he will be entirely lost and truly without help. Remind him of how you both fell in love. See if there are goofy ways to recreate things that remind you of those times. Try and do all you can to remind him that whilst he is carrying the burden of illness, he is still the man he was, somewhere in there.

It’s ok to feel tired, disgusted at times, and angry, disappointed, dissatisfied, taken for granted etc. Give him some time to turn his attitude around after the gentle talk. You might have to try this talk with him a few times. Listen to what he has to say, then give yourself room to say what you need to say. This change will not happen overnight. If he still won’t even entertain the idea of doing anything for himself, you might need to think long and hard about your own future.

sending love

Oh I've tried talking, I've tried yelling and screaming and shouting too. Yesterday he spotted the Postman coming to the door while I was in the kitchen. So he shouted my name. I stopped what I was doing to go and see what he wanted, and he got all hurt and surprised when I told him he didn't need me, all he had to do was open the app on his phone and ask postie to pop it inside the door.
He drops things and doesn't pick them up, theres a slow avalanche of discarded stuff beside his chair, which itself is slowly falling to pieces because he throws himself into it because he doesn't have the strength to do anything else. It used to be a recliner, but rats got into our last house and chewed the wiring. My son offered to look at it, but he refused. They were attracted by his stash of sweeties...
And please don't ask about his bedroom. The cleaner isn't allowed in there, I'm discouraged from going in there. I've already had to throw away one mattress because of the stains. He uses disposable pads on his mattress, but they get all crumpled up and stuck to his bum. Found one on the arm of his chair when I went into the living room yesterday morning...
Like you, I need physical touch, and love a good back rub, but if I wanted one, I had to ask, it was never offered. Infact he would say 'you only have to ask' and genuinely didn't get why that disappointed me so much. So I stopped asking.
He does have a good point, he loves the animals as much as I do.

OP posts:
RakshaUK · 12/10/2025 04:58

lambdressedasspam · 12/10/2025 02:07

If the doctor had of been more proactive with leg when you first went in, do you think it would have led to different circumstances?

Ÿes I think so. As I understand it, the lump is down to a blockage in the lymph system, leg ulcers are often caused by damage to the same system.
None of the Doctors he's seen have actually been able to give us any kind of meaningful diagnosis.
It feels like his case has been put on the Too Difficult pile.
We can't even get regular weekly visits from the District Nurse, sometimes is Friday, sometimes it's Saturday, which means I can't make any plans because I have to be around in case it's not one of our normal nurses who really love meeting them.

OP posts:
Bluecrystal2 · 12/10/2025 04:49

PhuckTrump · 11/10/2025 20:27

You lost me at shitty fingerprints all over the house. LTB.

Absolutely disgusting and there's no excuse for his filthy habits. I would insist on him going to a care facility and if he ever goes into hospital I would refuse to have him back home. How horrible, you've done enough for him.

SpaceCat3000 · 12/10/2025 04:27

Hi there,
I’m a little younger than you but in a similar situation. Both myself and my husband are disabled in different ways, and both have alot on our plates in our own ways. We both essentially care for each other, either one picking up the lions share for things the other really struggles with or simply cannot do. We’ve got it down to a fine art thesedays and when something new comes along (we jokingly say “oh well, just add it to the list of issues”) like a new medical problem on either side, we figure out who can do what, and do our best with it.

Now, my marriage is not perfect. I’m currently in a sexless marriage bevause hubbys pain and mobility issues really do a number on his libido etc, and while I also have 23/7 dreadful pain and mobility issues, I still have a high sex drive and would love any sort of sexual touch (doesn’t have to be sex, just close sensual touch etc). Alas, this is not to be and I’ve accepted that, I think.

Ive drifted from my point. What I’m trying to say is that while we both suffer with separate but quite rare disabilities, and we both have horrible relentless pain, we both do our absolute best for each other and for ourselves. I’m due for another round of physio? I’ll probably moan about it a bit, but give it my all and push through the pain with the guidance of my husband right by my side. Hubby needs another infusion which leaves him totally drained for weeks? He will moan about it but he will be there early for the appointment come hell or high water, and rest where he can for those weeks thereafter. What I’m trying to say is that we both get up, wash up and show up, for each other, for ourselves, for our kids etc. It sounds like your husband has let go of all dignity, and this is very sad indeed. For some years after my diagnosis, I would only wash when I could smell my own body odour, which I’m very ashamed to say.

I feel that from your post, you are being taken for granted and your husband had forgotten how important it is to get up, smarten up and show up for you, for himself, and for getting into the right frame of mind. You are wonderful for what you are doing.

I suggest a gentle talk. Ensure he knows that you find it an honour to care for him, and that you know he didn’t ask for this illness to happen. But it’s important to gently remind him that carers suffer from burnout, even carers who are wives. If he won’t do a thing to help himself, it’s making your job so much harder. If you burn out, he will be entirely lost and truly without help. Remind him of how you both fell in love. See if there are goofy ways to recreate things that remind you of those times. Try and do all you can to remind him that whilst he is carrying the burden of illness, he is still the man he was, somewhere in there.

It’s ok to feel tired, disgusted at times, and angry, disappointed, dissatisfied, taken for granted etc. Give him some time to turn his attitude around after the gentle talk. You might have to try this talk with him a few times. Listen to what he has to say, then give yourself room to say what you need to say. This change will not happen overnight. If he still won’t even entertain the idea of doing anything for himself, you might need to think long and hard about your own future.

sending love

Coaster99 · 12/10/2025 04:21

Oh dear, what a grim situation. Sorry OP, I’d just up and leave if I were you.

Idontknownowwhat · 12/10/2025 04:19

My advice to you, do all you can to get the support in place you need now.
Right now. MIL took on the lions share of caring for FIL until he died, which was quite similar to your situation.
I wonder, do ypu think it's possible that there's some Alzheimers in the background? FIL stopped realising he needed to wash his hands when his Alzheimers was worsening. He's in a terrible state by the sounds of it, but the way things are with our NHS, they'd allow you to pour into your partner until it puts you in a grave prematurely.
MIL was caring for FIL and they even let her go home to be his carer within hours of her waking from a radical hysterectomy.

JadedSoJaded · 12/10/2025 03:34

What do your sons think of the situation? Presume they live away from home?

CarlaLemarchant · 12/10/2025 03:26

I’m not as sympathetic to you as everyone else.
You shout in your OP “Why doesn’t he do something about it”. You are no better, you also have the power to change your living situation and you are not, it’s dragged on years. Leave or carry on as you are, it’s your life, you are choosing to stay and be his carer as much as he is choosing to refuse to improve his living situation. Someone above said co-dependent. I agree.

spoonbillstretford · 12/10/2025 03:24

Leave him.and let social services/his GP sort him out.

Franjipanl8r · 12/10/2025 03:13

There are no medals for women who spend their lives as servants to useless men. I’d have threatened divorce a long time ago.

Badger32 · 12/10/2025 02:49

Co dependent relationship
Your dependent on him as much as he is on you ( in your head you are )
Your autism has you stuck and unable to see a way out .
Your using your animals as an excuse for not leaving
Get to citizens advice bureau and find out how you force a sale through and yourself out of there
You might be able to get on the council list for a flat or get him on ..have you a social worker..you need one who can advocate for you ,not him .
For a start they should be putting carers in to wash and dress him ,not leave it to you ..if you start refusing to cook for him ,wash him ,or help him , social will have to get involved.
This will have to reach crisis point before he gets the help that will replace you
This is no life for you ,you must get help to get out of there

IShouldNotCoco · 12/10/2025 02:43

He sounds like my dad! My mum feels the same way you do but she married him, knowing full well that he’s like a child. I told her kindly she can’t expect him to change and he certainly won’t at 79!

Badger32 · 12/10/2025 02:38

My friend was in a similar situation with her husband,he had her doing everything for him ,he couldn't drive because he kept having fits ,he couldn't walk and used a wheelchair..the list goes on ..he became completely dependent on her for personal care tasks .
She managed to get him to stay with his mum for a weekend saying she needed a rest .
She packed all his stuff up , dropped it of at his mum's and changed the locks .
Within a year ,he was driving himself and had got a flat by himself, managing alone ..funny that ..
The more you do for someone,the less they do for themselves

lambdressedasspam · 12/10/2025 02:07

If the doctor had of been more proactive with leg when you first went in, do you think it would have led to different circumstances?

PardonMeNot · 12/10/2025 02:01

stichguru · 11/10/2025 21:40

Unless he's got severe dementia, sod him, even sod the pets, just run. Just set your self somewhere up to go, gather what you need and go. He's disgusting by choice. If he can pee in a washing up bowel, and walk to the loo for poos, he can wee in the loo and hit it. Walk away.

Most of us who have pets love them and consider them family members. “Sod the pets” is a terrible thought.

OriginalUsername2 · 12/10/2025 01:52

I think the poo on the walls would be the last straw for me. This is unacceptable from a man with full mental capability.

Have you started mentally making an escape plan yet? Do you work, have savings, any friends that could borrow the pets for a while?

Subwaystop · 12/10/2025 01:42

This is so sad to read. Sending love to you and the animals. I’ve been in a caregiver role with a very sick family member, which involved a lot of toilet cleanup. I often thought how deeply you must want to make another person’s life better to give so much of yourself. I’d never do it for someone who made me feel so awful. I hope you find a way to spend a lot more of your caretaking energy on yourself and the dogs and cats.

duckfordinner · 12/10/2025 01:41

He is mentally torturing you. Don’t be a martyr. Leave.

BankfieldForever · 12/10/2025 01:19

I love my husband but if I found myself in this situation I’d take the pets and leave. No question.

You can’t stay with him without the expectation by SS and NHS that you will be his full time carer. Tell whoever you need to that you refuse to provide any care at all and go. Anywhere, just go.

Its the only way.

ThisPithyJoker · 12/10/2025 01:13

Oh love. I honestly don't know what to say to this but I also didn't want to read and leave. This doesn't sound like a life for you, at all. Do you love him? Do you feel loved? Perhaps the answer to those questions will give you the solution x

Namechangerage · 12/10/2025 00:22

PhuckTrump · 11/10/2025 20:27

You lost me at shitty fingerprints all over the house. LTB.

Yep!!! This is totally disrespectful, unnecessary and disgusting. No matter how much mobility he’s lost, he can try and keep his hands clean.

Needspaceforlego · 12/10/2025 00:01

Lots of things to consider.
The house sounds perfect for you.
He sounds like a heart attack waiting to happen.

But it also sounds like he has MH issues.

I would try and ask for Social Services support. Even if he does need to pay towards careers.
And I'd be questioning where he in on the waiting list.