My Dad was dx w/Alzheimers about a year ago, and rec'd no medical treatment for it(was pretty "with it") until about 3 months ago when he was enrolled in a clinical trial involving
patchesAllergy testing
Skin color - patchy in Columbus, OH.
The problem is this: my mother was his
primaryPrimary amyloidosis
Primary biliary cirrhosis
Primary hyperparathyroidism
Primary insomnia
Primary lymphoma of the brain caregiver until her decline 3 weeks ago and she died this past Monday. My fathers condition began RAPIDLY deteriorating when she fell ill, and now needs pretty much 24/7 care (he wanders). The people involved with the clinical trial are discouraging us from dropping out of the study, saying "conventional" treatment "won't help anyway" and that we should just continue on.
My take is that the study
drugChemical dependence - resources
Chemotherapy
Drug abuse
Drug abuse and dependence
Drug abuse first aid
Drug allergies
Drug induced hypertension
Drug rash on the back
Drug rash, tegretol
Drug signs and teenagers
Drug-induced hypertension is not helping AT ALL, and due to the
rapidRapid shallow breathing decline we are noticing, I believe he needs to be on something else. I don't have a HCPOA, and my sister (who does) believes the study people.
What is the current standard of care treatment for Alzheimers? He needs assist w/most ADL, sundowns TERRIBLY, yet is relatively ok so far as
confusionConfusion
Delirium during the day. He occasionally hallucinates. He has declined so rapidly I see dramatic changes when I travel to see him weekly. He is being placed in a more appropriate facility next week.
If this were YOUR father, what would YOU do?
Thanks again.