@Greenfingers_girl, please don't take this the wrong way but I'm glad that you realise how exhausting it is looking after your Dad. You are doing it for a few days at a time though but your 80 year old Mum is doing it non-stop. Even if she's fit and healthy that's too much for her. I really feel that if medication doesn't improve things dramatically within the next few weeks then it's time for a care home. Being blunt, letting the situation run on indefinitely amounts to risking your mother's health for your father's wishes. It's really not uncommon for carers to end up predeceasing their PWD, sometimes quite suddenly. With dementia, you are often having to choose the least worst option. The carer's life is as important as the PWD's.
Hi, my dad’s now recently been on melatonin (in a dementia care home) and is finally sleeping at night after ages being up all night! Before being in care, at home he was literally up all night, wanting to go home (to his childhood home), wandering and eventually crashing out in the armchair for minutes at a time. Didn’t go to bed for months. My mum was absolutely exhausted. She slept on the sofa next to him for fear of him waking up and falling. I stayed with them for 5/6 days and was so tired after that short time!
Now he’s sleeping well and most nights in bed (can’t believe it) or in a recliner. (Please God it continues). Sleep is so needed!
Your mum is doing great, bless her.
Ask about Melatonin. Good luck.
@Violet Jane I don't take that the wrong way at all, in fact the last few days have been quite a wake up call. Since being back home dad has slept every night, all night on the Mirtazapine and Lorezapam - other than a couple of wee breaks. But as he's rarely napping in the day now he is needing more activities and is very lively. As much as it's nice to have my lively dad back he seems to be getting caught up in obsessive thoughts a lot which can escalate quickly, then disappear just as quickly.
I've told mum tonight that I'm calling the carer's organisation on Monday to start getting carers in during the day, as much as an enrichment for him as support and an ally for her, she finally said yes. If we ease her in gently then she will realise what a god send they will be and it will be easier to increase the amount of support during the day, which I know we will need. It will also be a professional voice to advise her, and us, going forward especially as she keeps promising my dad she'll never put him in a home. My mum can be oblivious to some elements of this situation but that is her personality and quite frankly I think that's why she's done amazingly for so long. And you sum it up perfectly
@Violet Jane it is about choosing the least worst option
@Julialou that is great news!! Like my dad too, long may it continue but I think we both know it probably won't. When I chatted with the Admiral nurse helpline last time they said my dad had probably moved beyond Melatonin helping and advised Mirtazapine. As he is sleeping on it I'm loathed to suggest moving onto something else!
I haven't cried yet about what's happening with my dad, perhaps I know I won't stop if I do or perhaps I know we need to be strong for mum. Maybe it's naive but I've always tried not to think too far ahead with this disease in regards to him. I have good friends who have lost parents or are going through it too so I accept what's happening but I always think don't mourn him yet, his funny, soft, gentle personality it still so much in there still.
I return back home tomorrow with a heavy heart but have one sister coming to spend the day on Sunday and my eldest sister coming on Wednesday to stop for a few days, I think they really need to see him in his current state to appreciate what extra support mum now needs. I'm also encouraging mum to call the GP on Monday regarding the day time effects dad's now experiencing.
Thank you
@Jaded'n'faded and all of you for your support and advice, it always seems so much bleaker this time of night it it's the only time I've got near my laptop!