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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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Thanks so much!
I'm just going to ask my doc, see what she says. Here, there is no one who gets intermittent resp support, it is never used as a treatment for MG. So, it is very different and it is expensive. But,for me it just seems like a healthier next step. Alice, do you have any advice I can use to convince my doc (she's saying; it's going to be rituximab and/or prednisonecocktail)? |
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