Hi All,
Just wondered if anyone else had had this experience. My mum had an official AD diagnosis a year ago, having suffered with dementia for about 10 years. Now it turns out that she has really high blood pressure and the GP says that's probably caused vascular dementia and that that is probably the main cause of her dementia. Apart from making me very thankful that I refused Aricept for her after it was awful for her sister (maybe she didn't have AD either??) I feel a bit non-plussed. Does it actually matter or make any difference to what would be the best way of caring for her? Obviously I am now administering blood pressure medication, but is there anything else? Also does it mean that if we control the bp she will be stuck at her present level of dementia indefinitely? That is an awful prospect as she's at that horrid stage of being aware there is something wrong and I have been thinking that at least she will lose that awareness eventually.
Just wondered if anyone else had had this experience. My mum had an official AD diagnosis a year ago, having suffered with dementia for about 10 years. Now it turns out that she has really high blood pressure and the GP says that's probably caused vascular dementia and that that is probably the main cause of her dementia. Apart from making me very thankful that I refused Aricept for her after it was awful for her sister (maybe she didn't have AD either??) I feel a bit non-plussed. Does it actually matter or make any difference to what would be the best way of caring for her? Obviously I am now administering blood pressure medication, but is there anything else? Also does it mean that if we control the bp she will be stuck at her present level of dementia indefinitely? That is an awful prospect as she's at that horrid stage of being aware there is something wrong and I have been thinking that at least she will lose that awareness eventually.