Hello all. Greetings from Canada. I have had MG since 1998 with Thymectomy '99, Radiation '99, Chemotherapy '99. Was good for a few years, and then Chermotherapy again in '06. We cannot get my symptoms under control with traditional methods anymore, and I have now started Cellcept.

I would love to hear from anyone who has been, or is on cellcept for myasthenia gravis. What I can expect, when, etc. We all know that you can read all the medical stuff you want, but it is in the personal experience of others that you gain the most insight and knowledge.

Thanking everyone in advance.