I´m thinking it sounds like a really stupid question, but I really needed to get some objectivity on my findings from an intelligent myasthenic mestinon user! Thanks Southblues!

It´s hard not having a neurologist. My doc prescribed it for me and he knows nothing about MG or medication……..YET!!!!

Just like you, I had lots of negative tests & many errands to the opticians! I had to negotiate with my employer for part time work since my lack of diagnosis would not allow me any paid sick leave. My energy just can´t get me through a 100% job any more. Admittedly my symptoms are quite tame at the moment but if I ever get another severe flare up in the future then I would hopefully know exactly which treatment to turn to. So in my case Mestinon might end up having more than just one job.

Nice to meet you and read your interesting posts


Anacrusis