My mum moved between care homes 4 weeks ago, 70 miles apart, due to the previous care home not offering dementia care. (Mum has Alzheimer's and vascular dementia.)
I wasn't expecting it to be plain sailing but neither was I expecting it to be so traumatic. Prior to the move she was content, in fact the weekend before I moved her we went out for a drive; for a walk in the park and for lunch.
Fast forward 4 weeks and she is now refusing to eat, drink or taking medication and now seems to be very depressed. She doesn't want to get out of bed, join in any activities, hates the new home and cries for most of the time when I visit.
Has anyone had experience of this?
The GP is visiting today and has mentioned that he may get the Crisis Mental Health Team involved. (There is additional concern in that she is diabetic and the lack of food and fluids obviously is making this worse.)
With regards to intervention, I'm quite clear on what I do and don't want to happen as the dementia worsens.
Can someone with experience of this please tell me what kinds of decisions I may be asked to make and how supportive you have found the home/health care time in supporting you in those decisions?
I feel like she's fading in front of my eyes and that I've caused it by moving her, although I had no choice.
I wasn't expecting it to be plain sailing but neither was I expecting it to be so traumatic. Prior to the move she was content, in fact the weekend before I moved her we went out for a drive; for a walk in the park and for lunch.
Fast forward 4 weeks and she is now refusing to eat, drink or taking medication and now seems to be very depressed. She doesn't want to get out of bed, join in any activities, hates the new home and cries for most of the time when I visit.
Has anyone had experience of this?
The GP is visiting today and has mentioned that he may get the Crisis Mental Health Team involved. (There is additional concern in that she is diabetic and the lack of food and fluids obviously is making this worse.)
With regards to intervention, I'm quite clear on what I do and don't want to happen as the dementia worsens.
Can someone with experience of this please tell me what kinds of decisions I may be asked to make and how supportive you have found the home/health care time in supporting you in those decisions?
I feel like she's fading in front of my eyes and that I've caused it by moving her, although I had no choice.