Hi Cooley - goodness, what a long time to have to wait for an MG dx. I'm curious too about your quest for an answer. I hope you feel comfortable sharing, because even those of us that have dealt with the disease and the neuro world for a long time get something out of new members experiences.

And I'm sure the experiences of others of us will help you as well! This is a very caring group of friends here - not just another forum, and they have helped me alot and I have learned more here than in hours of research! Personal experiences are so much more real that what you can read the websites - here we get to know each other and information comes out that the researches just don't know, it seems.

So feel free to join in when you feel up to it. What are they doing for you now that you have the dx? Whatever it is, I hope it has a dramatic affect for you and get's you strong quickly!