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Inconclusive Does Not Mean Nothing is Wrong
So many Lambert-Eaton Myasthenic Syndrome patients talk about how long it took to get to diagnosis. For me, it took decades. Here is a bit of my background story in the years leading up to my LEMS diagnosis, read by LEMS patient and forum member, and my friend, @pricewool. It’s less than 5 minutes to listen to. Take a listen and let us know, did you experience any of the same invisible symptoms that I did?
https://soundcloud.com/lemsnews/inconclusive-does-not-mean-nothing-is-wrong
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