The main purpose of this website is to help others learn more about the terrible disease called MSA. (Multiple System Atrophy) We have spent countless hours researching Dennis’ symptoms and praying we could find a doctor to help us understand what we were seeing. Finally, after more than 3 years, we at least have a probable diagnosis and there is proof of what is causing all of these symptoms. This is not to say that it is easier but at least we don’t feel as if we are imagining things. If we can reach a hand full of people with this site, that would be worth all of the effort. This is a very rare and un-recognized disease. We hope to help change that.