This is a very moving website. My husband does not have MSA, but Lewy Body Disease. However, the physical struggles are so similar. Any brain disease is horrific. My husband is now in a geriatric psychiatric hospital and it’s unknown if it will help. He can no longer walk and has become quite delirious, which is why he’s at the hospital. This is my first post, although I’ve been wanting to contact people struggling with similar situations to know I’m not alone.
Thank you for your wonderful website, story and assistance.