Hello I just joined Neuro Talk this moment. I have been reading posts for a while though. I got my good news in 2007 but went into remission, until middle of this year. The memory loss thing is a big problem for me also. I decided to join this forum simply to say what I think everyone with MG is experienceing. The Doctors look at you when you describe your symptoms like no thats not part of the diseas. Yet when I investigate myself I think many of us have the same symptoms. I find it comforting at least I am not crazy. Thank you all. Question. I'm on the pyra, and the pred anyone else haveing trouble distingushing side affects and actual MG?