Myasthenia Gravis Community Group
Pretty simple: I would love to engage/communicate with those dealing with the daily struggle of having Myasthenia Gravis. My world as I knew it, no longer existed when I was diagnosed with MG in 2013 ( it took a year to get diagnosed). Sometimes, I feel like no one truly understands this limiting, unpredictable chronic autoimmune disease.
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Hello, a few days ago i saw a new neurologist and he said i most likely have Myasthenia gravis due to my severe... READ MORE
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My husband was diagnosed with mynacenius gravis in February, 2019 and currently receives infusion treatments twice a... READ MORE
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seeing specialist Tuesday from docs referral for possible MG. The symptom I went with was spontaneous monocular ptosis.... READ MORE
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I booked an appointment to get fillers done and apparently it shouldn't get in the way of MG. Anyone had fillers done?... READ MORE
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Hi I am in need of some support... the doctors tell me that i have conversion disorder or a complicated migraine. They... READ MORE
