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Originally Posted by Denise9293
Since December 2013, I have had extreme fatigue and muscle weakness in my limbs. Also experience trouble swallowing and shortness of breath. My neurologist was at a loss but decided to try Mestinon. Symptoms have improved some but I now have twitchy eyes and muscle cramps from the med. I was told that 5% of MG patients test normal. How can I just accept that diagnosis without proof?
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My neuro told me that somewhere around 10 percent of MG sufferers are negative on all tests. They are diagnosed by presenting symptoms and response to mestinon.