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because my MG symptoms have been under decent control, I try not to mention it very often. I have recently retired and medications have been working (Cellcept and Mestinon). Biggest problem is discussing MG with providers other than my neurologist. I find you need to be VERY up to date on medications that may increase your symptoms and often providers really don’t listen. They want to throw you a medication to ‘fix’ something without much thought about underlying conditions.