← Return to Looking for someone who has axonal sensorimotor polyneuropathy

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@celia16

What were your EMG results?

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I was diagnosed in the summer of 2016 with severe axonal sensorimotor polyneuropathy. I was put on loads of medication’s to try and numb the pain. After going through the Sanexas treatment, I am no longer on those medication‘s, and the pins and needles are 95% gone, and so is the pain