People with MG, have you ever done IVIG for the first time and have it not work well? Did it take multiple infusions to see results? I had one ivig treatment, it did not give the “180 degree turn around” “miracle treatment” effects that my neurologist (not an mg specialist) said I would have, so he said I don’t have MG anymore? Im not sure what to think.
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Yes, some people with Myasthenia Gravis have reported not experiencing significant improvements after their first round of IVIG treatment. It may take multiple rounds for some individuals to see noticeable results.
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