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Myasthenia gravis: What do you think about your treatment?
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MaggieMG
@Courtney_J This is all still a bit new to me, and so far I've only been given pyridostigmine, so I'm not sure if I can give a review of sorts. I think it's helping my MG, but it makes me feel truly awful. I'm thinking about asking my doctor if there's something else I can take
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MaggieMG
@Courtney_J My symptoms came on rather suddenly, almost overnight. I thought at first I was having a stroke because you hear about the face drooping when that happens. Then I thought it was stress or fatigue but then when it didn't go away I knew it was something else. I went to my GP who told me to go to an eye doctor. Then there was some back and forth with the GP who finally ordered tests for me. It was awful waiting for the test results.
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MaggieMG
@Courtney_J My symptoms came on rather suddenly, almost overnight. I thought at first I was having a stroke because you hear about the face drooping when that happens. Then I thought it was stress or fatigue but then when it didn't go away I knew it was something else. I went to my GP who told me to go to an eye doctor. Then there was some back and forth with the GP who finally ordered tests for me. It was awful waiting for the test results.
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Courtney_J
Community managerGood advisor
Hello everyone,
How are you today?
Let's talk about some of the treatments for myasthenia gravis (MG)!
Are you taking or receiving any treatments or medications for your MG? If so, what kind? What do you think about it? Is it helping?
Let's share together here!
Take care,
Courtney