Hi--I'm afraid I don't have much to say that will be helpful, but I am so sorry you're going through so much.

Most of us here have two things to go on: our own experiences with MG, and what we've read about MG. But none of us has all the possible symptoms (at least I don't think so!), and all of us know that there are real MG symptoms that don't show up on the lists.

You say that three doctors ruled out the possibility of MG because you don't have eye involvement. Yet my neuro tested me for MG antibodies (just a blood test) and ordered a single-fiber EMG before my eye symptoms started.

Again, I'm really sorry I can't offer any practical advice. But welcome to the group. I'm new here, too, and you're right--this is a caring community.

Abby