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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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Junior Member
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Hi All, I am new to the Board, I never thought I would be in this spot again. 17 years drug and symptom free and three weeks ago symptoms came back with a fury. Many years ago I was very involved with the MG Foundation in California and learned to be my own expert in my disease. My GP has put me on Predisone 20 mg a day and 60 mg of Mestinon every three hours but the weakness is still interfering with my ability to function. I have an appointment with a Neuro on October 5th finally. Just hoping he has treated others. So Many things have changed in treatment in the last 17 years. I don't know were to start. Thanks for Listening. I really need the support now
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