[Aviator1]

Hello All:

I joined here in February after being diagnosed with MG. My neuro started me on 60 MG Mestinon, 3 times per day. I had no side effects.

I would sometimes forget my afternoon dose, and found I felt no different than before the diagnosis.

I then started skipping the evening dose, and for the last month have been taking none.

I feel better than I have for many months. No problems with breathing or swallowing. I still have some slight diplopia at times.

Any ideas, suggestions, comments?

Thanks and God Bless.