October 3 is officially National Multiple System Atrophy Day, (M.S.A.) It is a day to make others aware of this rare illness. I suffer from this condition--another term is olivoponto cellebrar degeneration. Help the ill and their families get the word out that WE WANT and WE NEED a cure.
I have added a MSA blog page to website www.kathyjwhite.com Makes more sense than having 2 separate websites. Also switching providers, so things will be new and different and somewhat a "work in progress".