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Dementia and Alzheimer's

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Near the end but not imminently

3 replies

Imamumgetmeoutofhere · 14/02/2026 16:16

My wonderful father in law was diagnosed with mixed dementia consisting of vascular dementia and Alzheimer’s about 11 years ago.

The first few years were slow in progress. About 5 years after diagnosis things started to get worse at an increased rate with him wandering off, getting aggressive verbally and physically then declining further where he couldn’t wash himself and became doubly incontinent.

My mother in law was his main carer and and me and my husband would take turns in going in to see him in the mornings / after work and then we would take the kids in the evenings and weekends (they are now 18 and 12).

2 years ago he went into a care home as none of us could cope anymore with having him at home, with all the violence, toileting and washing issues and not really eating or drinking properly as he couldn’t feed himself but wouldn’t let us feed him.

It came to a head after he fell at home and we had to wait 4 hours for an ambulance with him laying there with a broken leg and soiled himself but getting distressed and shouting then crying. Then social services got involved, came and did an assessment and said it was best and we agreed.

We cannot fault the care he’s had there, carers are so kind, compassionate and seem to have plenty of time for him and to answer any of our questions when we are visiting.

He’s recently had a chest infection, then an infection in a wound on his foot. And he had a fall out of his bed which meant he had to go to hospital.

Weve signed a DNAR which was heartbreaking doing it but it felt the kindest thing to do.

He has now refused to eat anything. Nothing mashed, nothing pureed. He will only drink water, tea or Pepsi. He doesn’t know who any of us, can’t remember where he was born. He no longer talks at all and just sits there bashing his side table with his hand.

He’s lost a significant amount of weight in the last few weeks. A hospital admission was tried to give him a drip etc but he kept pulling it out and shouting he wants to come home so we’ve as a family agreed to this for the time being.

Weve been told that if he doesn’t eat then he will die. How long this is, they cannot say. Could be days, weeks or months but that we are now treating him as end of life. He’s sleeping a lot more now and is harder to rouse.

I don’t know why I’m posting really. Just sad it’s finally come to this. Sad for my mother in law for losing her husband she’s been with since she was 17. Sad for my husband who’s going to lose his father. Sad for my children losing their grandfather.

OP posts:
Justbecauseyoucandoesntmeanyoushould · 14/02/2026 16:39

I'm so sorry. It is very sad. Lost my GM and DM to dementia (DM quite recently), and my DH is about 8 years into his dementia adventure. All had/have no quality of life and no prospect of recovery or even improvement in their condition.
Dementia is a very long goodbye. By the time you get to the end, you've already done most of the grieving. Acceptance of their death comes more easily, I found.

FinallyMovingHouse · 14/02/2026 16:40

Hi OP, It's horrible isn't it.

My DMum is currently in a very similar situation, after starting to refuse food and drink several weeks ago. She's gone downhill more rapidly in the last week and is now in bed and only occasionally conscious. She's not eating any more and may take small sips of lemonade, but that is not often and she is clearly finding swallowing hard.
My Dsis (ex ITU sister) and I hold POAs for health and wellbeing and we have been very clear that she has a DNR and that we don't want a hospital admission for her. (She hated being in a hospital just before Christmas).
The care home are behind us and have sorted meds to help with night-time hallucinations and the only aim we have is to help her to stay as comfortable as possible through the end of life process.

Sending prayers to you all x

Imamumgetmeoutofhere · 14/02/2026 20:12

It’s just so shit. I’m so sorry you’ve both had to experience this awful awful disease with your loved ones too.

It’s so painful as you lose them again and again each time something is lost. Then again when the pass away.

We know the end is coming but the being in limbo is awful 😢

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