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Elderly parents

Just a moan

9 replies

LawrieForShepherdsBoy · 22/10/2024 20:10

Cause DH is sick of me banging on about my parents and I need to get it off my chest.

Both parents with dementia, dad early stage Alzheimers, mum mid stage rare ftd. I’ve been staying with them for a week a situation with live in care. Changing agency, all quite difficult and I’m probably here til a couple more days.

My mum can get really anxious, and when she does is really stuck to my poor dad like glue.

My mums anxiety has been off the scale since yesterday lunchtime. Rolling waves; it’s awful to watch. Last night was so tough. My dad and I tag teamed it, and I got no sleep at all.

Unsurprisingly, my mum is completely wrung out now. We getting a home visit from dementia team tomo and they suggested giving her the higher dose of sleeping pill tonight than we normally do.

We’d eaten by 530, meds all done, my mum was relieved it was the end of the day. But here’s the thing, she won’t go to bed til my dad does. This is quite common, but does depend on her anxiety. When she’s okay she will take herself off to bed but when she’s struggling there’s no chance. Even walking into her bedroom is difficult (they’re in separate rooms). Trying to get her to bed will just make things worse.

My dad needs a break. He’s done in. He wants to watch You Tube. I text him once it got dark at 630ish to suggest he pretend to go to bed. My mum would have been in bed and asleep within half an hour and he’d have the whole evening. But nope, he not going to. He blasting the TV so loud which so difficult for my mum. Her anxiety is building up. I can’t do a repeat of last night. It was awful and today has been terrible too. It’s too late now anyway. If he’d gone earlier, he could have got up again and had that alone time. I know I sound hard - I know he has dementia himself. But he’s v early stage and he’s the only one who can act to maybe make next 24 hours better for us all.

There’s nothing I can do. Any attempts to get my mum to bed will make everything worse. If I suggest he turn the tv down, it will make it worse. If I go back downstairs, it will set my mum off. I just have to stay calm and away. Avoid escalation and hope my dad doesn’t stay up really late.

Grrr 😡

OP posts:
ZippyDoodle · 22/10/2024 20:32

The best thing for dementia is routine. You may not manage it in the next day or so but new carers might.

Do the same thing every night. Maybe play a nice soothing song your Mum likes. Change into pyjamas. Have a nice milky drink. Clean teeth. Wash face. Sit and chat. All nice and calm. Maybe even get her a teddy bear to cuddle.

How about headphones for your Dad?

6.30pm is very early to go to bed. That may not help the situation.

It will get tougher, sorry.

LawrieForShepherdsBoy · 22/10/2024 20:46

Absolutely to routine. My mum really needs it. She wouldn’t usually go to bed any time near 630 but she got less than three hours sleep last night.

But luckily she’s self soothing nicely in the kitchen. There will be dirty plates and fresh yogurt in the cupboards tomo but she’s okay. So I guess my dad was right and I was wrong dammit 😉

OP posts:
LawrieForShepherdsBoy · 22/10/2024 20:53

I didn’t really mean the dammit. I’m very okay with being wrong right now. Im going to risk re-doing her hot water bottle.

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SockFluffInTheBath · 24/10/2024 18:12

@LawrieForShepherdsBoy how are things this evening? I hope the new agency is working out,

LawrieForShepherdsBoy · 27/10/2024 14:25

@SockFluffInTheBath it’s been good and bad. I’m back at home now after nine days. New carer started yesterday. A temporary one til long term carer in a week. She seems really good but I am so mistrustful nowadays.

my mum had another bad night. Maybe Thursday? My dad was stressed all day and that impacts my mum. And she knows I’m annoyed with him, so my presence not helpful at this point.

But good news. We have a local service called Dementia Intenstive Support Service. I’ve never used it but I rang them on Tuesday. Home visit on Wednesday from this amazing woman. She was so good with both my parents, really respectful and warm. She did an assessment and rang back later that after MDT to say they will take my mum on.

Basically it’s a six week intervention during which we will hopefully be able to have an impact on my mums anxiety. There will be weekly home visits and also a weekly phone call. Doctor should be in contact with me tomorrow about medication options. Nurse from the team came round yesterday to do bloods and ECG. Basically ruling out anything physical. The nurse was awesome. After bad experience with last live in carer, my mum won’t undress and becomes distressed at the suggestion. Nurse did the ECG with my mum fully dressed, so calmly.

Im hopeful that this service may be able to help. I’m really happy the service exists and impressed with the two people I’ve met so far.

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SockFluffInTheBath · 27/10/2024 15:59

That sounds fantastic. Not out of the woods but having the right support makes a significant difference. I hope you feel you can breathe a little more now.

ChimpanzeeThatMonkeyNews · 24/11/2024 22:02

How are you doing @LawrieForShepherdsBoy ?

LawrieForShepherdsBoy · 30/11/2024 08:26

Ups and downs. This week has been hard. My mum had two different medical appointments: the first one she had complete meltdown at hospital so they couldn’t do procedure. Second one we couldn’t get out the house - not anxiety related.

I need to be on the front foot with medical stuff. Just need to really push and advocate for her to access healthcare.

In good news, new live in carer is good. She’s their main carer, will work a five week on/two week off pattern. And I know the carer who’s covering the next two breaks and sues great too.

But then in bad news my parents got grifted for third time in last eighteen months. Which has really pissed me off. But not as much as first two times - I have lowered my expectations of humanity a bit.

OP posts:
TinyMouseTheatre · 30/11/2024 13:44

I'm so sorry about the grifting. Are you able to move their money so that they don't have the same access to it?

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