Thanks for asking. She's on a slow steady decline. At this point we've accepted the inevitable. All they do is treat the symptoms. Nothing is going to bring her even remotely back. I've always respected my dad but that has grown exponentially. It is very frustrating to deal with her, she can never be satisfied. If she is home she wants to be going somewhere. When she gets somewhere, she wants to be home. If she's standing, she wants to be sitting. If she's sitting, she wants to be standing. My dad handles that with the patients of Job. It's hard for me not to get angry with her and he reminds me that "it's not your mother." I think the disease has caused her to be bi-polar.
Dad and I have been to multiple Alzheimer's informational meetings and we know what's to come. It ain't pretty. My hope is dad doesn't wait too long before getting help,/placing her in a home. Years go they both purchased long term care insurance but it has it's limits of coverage. It's very good coverage but once the benefits are exhausted it's pretty much gone. Because of this he's worried she'll outlive the benefits. Physically she's in pretty good shape.
Lots of challenges ahead. All prayers are appreciated especially for her and my dad.