I'm hoping that someone out there may have some advice or words of wisdom for the circumstances that my husband and I currently find ourselves in.
My mother-in-law was diagnosed with vascular dementia and atrial fibrillation in 2016. Physically she is very fit and does a lot of walking but her day to day memory and general confusion has steadily got worse. Whilst she can dress herself, she tends to wear the same clothes all the time and nothing ends up in the wash and she does not shower or bath but tends to use talc to mask anything. She can also forget to eat or drink unless prompted. She was prescribed medication back in 2016/17 for the dementia and atrial fibrillation which she has refused to take and she won't go to the doctor.
Her husband is currently at end of life and has just moved from the local hospital (where we were able to visit him quite regularly via appointment) to a home where we are restricted to seeing him once a week. Sadly the local Hospice has no available beds.
We all live together although, up until this Spring, my in-laws spent all their time abroad (Portugal in the Winter and the USA in the Summer). My father-in-law did everything in terms of organisation, cooking meals, shopping etc. She hates being in the UK and her kneejerk reaction is to book a flight to the USA so she can be with her daughter. There is no way she could negotiate two international airports on her own and overseas travel is not exactly encouraged right now!
We are really struggling to explain why she cannot visit her husband at the moment. We've had some episodes of paranoia and accusation already and we are desperately worried about how my father-in-laws impending death will effect her, especially if she is not able to be there at the end.
My husband and I and our teenage son all work so she spends several hours at home alone each day. She goes out for walks and we have no fear of her wandering off as she is very familiar with our surroundings, but the time spent alone is undoubtedly not good for her. I fear that bringing up the subject of a carer coming in will not be met with open arms, especially as her long term care plan is "Put me on a train"!
So, any encouragement, advice or shared experiences would be very much welcome!
My mother-in-law was diagnosed with vascular dementia and atrial fibrillation in 2016. Physically she is very fit and does a lot of walking but her day to day memory and general confusion has steadily got worse. Whilst she can dress herself, she tends to wear the same clothes all the time and nothing ends up in the wash and she does not shower or bath but tends to use talc to mask anything. She can also forget to eat or drink unless prompted. She was prescribed medication back in 2016/17 for the dementia and atrial fibrillation which she has refused to take and she won't go to the doctor.
Her husband is currently at end of life and has just moved from the local hospital (where we were able to visit him quite regularly via appointment) to a home where we are restricted to seeing him once a week. Sadly the local Hospice has no available beds.
We all live together although, up until this Spring, my in-laws spent all their time abroad (Portugal in the Winter and the USA in the Summer). My father-in-law did everything in terms of organisation, cooking meals, shopping etc. She hates being in the UK and her kneejerk reaction is to book a flight to the USA so she can be with her daughter. There is no way she could negotiate two international airports on her own and overseas travel is not exactly encouraged right now!
We are really struggling to explain why she cannot visit her husband at the moment. We've had some episodes of paranoia and accusation already and we are desperately worried about how my father-in-laws impending death will effect her, especially if she is not able to be there at the end.
My husband and I and our teenage son all work so she spends several hours at home alone each day. She goes out for walks and we have no fear of her wandering off as she is very familiar with our surroundings, but the time spent alone is undoubtedly not good for her. I fear that bringing up the subject of a carer coming in will not be met with open arms, especially as her long term care plan is "Put me on a train"!
So, any encouragement, advice or shared experiences would be very much welcome!