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Were you given any information about Myasthenia gravis along with your diagnosis?
When you were first told that you had or that you potentially had Myasthenia gravis, were you given any information about what MG was?
What did this “information” look like? Did they give you a short-minute verbal description? Did they give you any written or typed information on paper to take home?
Did they send you off on your way with a game plan, doctor referrals, and an appointment in which you could get started with treatment?
Or did they give you nothing?
How did it make you feel?
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