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Dr. Diana, both a doctor (therapeutic optometrist), and a recovered POTS and ME/CFS patient, offers help and hope for POTS, Dysautonomia, Ehlers-Danlos syndrome, Chronic Fatigue, Chronic Lyme, vascular abnormalities, Fibromyalgia, and Multiple Sclerosis. Dr. Diana is now working full time at POTS Care.
NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › Vision › Myasthenia Gravis
Has anyone else ever been diagnosed with this? My eye Dr. thinks I have Myasthenia Gravis. My eye muscles are all either very weak or paralyzed. My throat seems sslightly affected. I am such a nervous wreck since this appointment because she mentioned this possibility as well as Mitochondrial Disease. She said time is of the essence and I am already farther progressed than some other patients she has seen : ( Any advise or support is very greatly appreciated.
I had the diagnosis for 7 years prior to heading to the Mayo clinic and getting the real story, it wasnt MG. Do you have positive antibodies and have you had a single fiber EMG which will tell the story its its MG. Most cases of MG can be well controlled with mestinon and immunosuppresants. I also had the droopy eye (ptosis) and swallowing difficulties. Make sure you are getting the right test by a center and doc that specializes in MG.
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