My Dad moved into a care home just over 3 weeks ago following almost 4 weeks in hospital. So far he seems to have accepted the move and as yet we haven't had any questions about when he's going home.
Since he went into the care home his mobility has declined - he now uses a frame rather than a stick, and that's on good days - they often use a wheelchair to move him around too. What started as night-time incontinence when he went into hospital (there were never any problems at home) has become daytime incontinence as well and he has been assessed for incontinence pads. Yesterday it took 3 carers to dress him as he had no balance and he was very sleepy and vacant when I visited in the afternoon - I looked into his eyes and got nothing back although he knew I was there and who I was. Anything he did say was incoherent. So I suppose my first question is, is this rapid decline unusual? He was only diagnosed 3 months ago although we of course knew there was a problem long before. Is it common for people with dementia to decline after going into a home? Or is Dad just generally suffering a rapid decline and his environment is immaterial?
On Friday we had a financial assessment by Social Services. It seemed that there would be one weekly cost if he contributes and the County Council loan the balance until his house is sold, and a different weekly cost if Dad was paying the whole cost directly out of private funds (he would pay £200 more in the latter). Is this common?
Finally on our calculations, Dad's funds would run out in less than 2 years (he has no savings, only equity in his house) and so a big question for us then is can the county council force us to move him to a cheaper home if they are footing the bill?
Sorry for all the questions and thanks for reading
Since he went into the care home his mobility has declined - he now uses a frame rather than a stick, and that's on good days - they often use a wheelchair to move him around too. What started as night-time incontinence when he went into hospital (there were never any problems at home) has become daytime incontinence as well and he has been assessed for incontinence pads. Yesterday it took 3 carers to dress him as he had no balance and he was very sleepy and vacant when I visited in the afternoon - I looked into his eyes and got nothing back although he knew I was there and who I was. Anything he did say was incoherent. So I suppose my first question is, is this rapid decline unusual? He was only diagnosed 3 months ago although we of course knew there was a problem long before. Is it common for people with dementia to decline after going into a home? Or is Dad just generally suffering a rapid decline and his environment is immaterial?
On Friday we had a financial assessment by Social Services. It seemed that there would be one weekly cost if he contributes and the County Council loan the balance until his house is sold, and a different weekly cost if Dad was paying the whole cost directly out of private funds (he would pay £200 more in the latter). Is this common?
Finally on our calculations, Dad's funds would run out in less than 2 years (he has no savings, only equity in his house) and so a big question for us then is can the county council force us to move him to a cheaper home if they are footing the bill?
Sorry for all the questions and thanks for reading