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Affected... I could have written what you wrote. My husband won't see a dr. Since our first clinic visit. I had to lie the 2 times I got our family dr to come to the house . He fought with me he didn't want him here....was as nice as can be to the dr. Agreeing with whatever he said...then...

Patcook Check with your insurance company first sometimes they cover the costs.

My husband has had shoulder pain. When his legs were starting to give him trouble he was pulling himself up which caused issues like frozen shoulder ...physical therapy really helped.

Thank you both for advice. It helps to hear that someone truly understands. I think the bottom line is that it is what it is...and it is an impossible situation. I will ask for medication to see if something will help. We have Marinol which is pill form of synthetic pot which does seem to help...

My husband was diagnosed the end of last summer. His is very fast moving, sept he was walking Dec he wasn't . He has no use of his hands and has very little speech left. He refuses to see a doctor since our last visit to a clinic in dec.. I think he doesn't want to hear bad news...like he lost...

I am looking to talk to someone who has experienced the dementia part....

I have been reading your posts and we have a lot in common...people don't have a clue how this disease effects everyone in the family and how hard and demanding it is.... I am near my breaking point...my kids have seen me lose it and yell at my husband...then I feel guilty... I can't win no...

I am sorry for your loss....I know I will be going done the same path . My Husband was diagnosed 13 months ago. .... And I was never sure if he had the dementia part. I was hoping you might help me.... You say he wasn't the husband you knew....sometime my husband seems like himself and others...