Thank you all for your replies. My SFEMG isn't scheduled until May 8th at the U but fortunately, my symptoms have not impacted my daily life (especially with Mestinon response). I did reach out to my neuro-ophthalmologist to ask about dosage. He recommended I stick at this dosage for a bit and see how the body responds and we'll connect early next week.

Annie, any local recommendations you have (Docs, etc.) would be welcome. As of now, I will primarily be engaging at the U but if I get a positive diagnosis, I would welcome feedback on comparing long term care/support between the U and Mayo.

For everyone else out there, thanks again for reading and your support. I look forward to getting answers and sharing with you all soon.