Thanks for the responses.
Myasthenia Gravis has not been eliminated. I am almost afraid to hope for that.
Yes, I am trying to stay positive but the reality is that my mother, who also lives with me, is physically disabled and my father is her primary caregiver. So I do need to do some serious planning for the worst case scenario. If it doesn't come to be, great. But if it does and I'm not prepared it will be a disaster.
So next step: neurologist. Anybody have any recommendations for neurologists in San Francisco, preferably affiliated with UCSF. Stanford is also in option. We live halfway in between the two facilities. We are extremely lucky to have easy access to excellent health care.