← Return to Anyone been treated at Mayo Clinic for Ocular Myasthenia Gravis?
DiscussionAnyone been treated at Mayo Clinic for Ocular Myasthenia Gravis?
Autoimmune Diseases | Last Active: Feb 5 9:49am | Replies (37)Comment receiving replies
Replies to "Hi @wcburns2, I expanded the title of your discussion to reflect your question and included it..."
Thank you for tagging me. When I went to Mayo last month, I had several tests, with the main 1 being the ENG, and Myasthenia Gravis was ruled out. I was diagnosed with Parkinsonism. I do have several symptoms of PD, but they are very slight but seem to be increasing. So I will continue to see how I progress.
Hi Colleen. When I first posted you helped out with tagging or broadening my potential reach. Does that happen automatically now if I post? I am nit exactly sure how to navigate within Mayo Connect. I posted a follow up to my condition this AM about my visit to Mayo six months ago
Thanks
Bill
Could you describe some of your experience with ocular MG?