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From my time on the MG forums back when I was having the bad time, it appears to me that we all have our own version of MG, our own path through treatment, and our results vary widely.
I had worked in medicine as a researcher for 25 years before I got MG. I think that gave me much more confidence to try to take on my own treatment, especially in things like tapering medications and taking them as needed (mestinon).
One hopes that our neurologists have experience in MG, are up to date on new treatments and have the time to really concentrate on our own case. However, that is being very optimistic!
Good Luck
Russ