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Does anybody have experience with SANEXAS for neuropathy?

Neuropathy | Last Active: Jul 8 11:13pm | Replies (270)
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@jzxbb

Thanks for your consideration.
I've seen in about 45 years almost 250 Doctors in the NE with no luck including Hopkins, U of MD and Hershey but this is totally weird.
Considering how long it's lasted and how extreme it is I'm sure the Sanexas had no part in it but who knows. Frankly I can barely walk or drive so everything is done for me now. Thanks a lot anyways but my life is over now. 250!!!!!! cmon!

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Replies to "Thanks for your consideration. I've seen in about 45 years almost 250 Doctors in the NE..."
John, Volunteer Mentor | @johnbishop | May 12 8:11am

That is a lot of doctors and still no help. It sounds similar to this persons journey.

What happens when you have a disease doctors can't diagnose TED talk by TED Fellow Jennifer Brea who became progressively ill with myalgic encephalomyelitis, commonly known as chronic fatigue syndrome.
-- https://www.ted.com/talks/jen_brea_what_happens_when_you_have_a_disease_doctors_can_t_diagnose

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