Does anyone have any advice on help with coping with a partner who spends the majority of the night in and out of bed? I have asked for sleeping tablets for him but been told the problems if taking them not the benefits and I still struggle on. What about the carer who gets very little sleep?
With you working full time this must be a major problem.
When my husband came back to live at home after he was diagnosed with ATD I went for separate living areas. As his night time walking became a problem, frightening me standing by my bed in the dark, I put a heavy lockable door to his rooms. This meant he was safely confined at night, away from the fire, and the kitchen.
Every night I explained about it and that he was to bang on it if he needed me. After a few weeks he accepted it. This meant I could have people to stay, without him going to respite. I was better tempered, Gp gave me some sleeping tablets for occasional use.
I often would check on MH in the night and was amazed to find he had learnt to use his CD and radio, after a gap of years, (I'd reduced the Aricept) and was often just sitting listening to music.
Later on, I used to get up in the night and have a mop around ( I threw out the carpets) so he wasn't paddling in his own urine. Make him a drink and a sandwich etc.
Things got calmer for a while and it meant he could live at home longer.
I realise a lot of houses wouldn't lend themselves to doing this.
But a big bedroom? Small ensuite?
Just an idea.