Snowy Lynne, your posts are encouraging. My husband is also on Reminyl. His doctor leaves it to me to call and tell him when I think the dosage needs to be increased, which is very difficult.
I wonder if his dosage is increased now, if the time when Reminyl is no longer effective will happen earlier.
I had heard they were trying immune system treatments because they might clear some of the beta-amyloids. I didn't know this had gone past the research stage? Do you have any information on this?
Not me.When I was diagnosed nearl 9 yrs ago I wan't on anything until 2 yrs later,& then I was on Aricept.After 4 yrs it stopped working & was put on Reminyl.I was asked to be in a study but refused,I wanted the medication then,not a placibo. Still doing very well & intend too for a few more yrs yet.
