Alissa,

I am glad you found this site. I understand how you feel-but try to educate yourself & be your own advocate. It is also important to be direct w/ your neuro. Keep the faith. I know it is hard. I was diagnosed in March of 2007 and at this point Mestinon is not controlling my symptoms enough. I cannot take steroids-long term and I had an awful reaction to IVIG. But remember MG affects everyone differently so keep that in mind. You are in my thoughts & prayers. Let us know how you are doing. This is a place of support and information(from people who really get it). Take care of yourself. Peace.

Nancy Lee