I have come a long way since my MG diagnosis in July 2020. I saw my specialist today. My eyelids were even and the twitching is reduced, double vision is reduced. I haven't used my eyepatch since I started Mestinon, and I'm not nearly as clumsy as I used to be. There is still a ways to go, therefore; we have increased my dose of Mestinon and complete two more tests. The first one we are doing because I can't convince anyone in the city I live in to do: an actual scan of my thymus
and an EMG.