Sorry if this sounds more dramatic than it ought to but looking for some advice in case needed.
DF was admitted to hospital following a fall. He's ok but also has dementia so he's not settled very well. He's now been there for over a week while they work on his mobility.
The plan at the moment is to discharge him when he can walk better but in all honesty he's walking less there than at home- he's sitting most of the day.
The drs are talking about a multi-disciplinary approach to his future care including adaptations at home- like lots of hand rails, equipment etc so it's safe for him.
My mum is a bit shocked at this- she's cared for him for 3 years and they manage quite well. She's not delighted at the idea of lots of rails around the house partly because she doesn't think it will help dad anyway, but also- they are on a small budget- she's recently paid for lots of decorating, home improvements etc , which in her eyes would be 'ruined' by mobility aids she doesn't think would help him. I don't want that to sound selfish- mum has devoted herself to his care for 3 years and is in her 90s too.
As a general point, can we as a family ask for his discharge from hospital even if he is not 'ready' in their eyes and also can they force mum to make her home 'suitable' for him against her wishes?
It seems he is now in the system and being processed, without family wishes or input being taken into account.
Does the state 'own' his care rather than family? (my mum, me and my brother had POA.)