I was diagnosed with MG at 40 years of age. I was scared because I had never heard of it and I think a neurologist is one doctor you don't really want to have to go see. I have 2 young children, I am young! The MGA Support Group calmed me down, helped me understand MG and I have always felt that they could help me through this. The newsletter is great, in the years that I have had MG, it has grown as the Association has. They seem to have attracted some very sharp individuals who have really increased the energy and reach of this organization. Bravo!