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Does anybody have experience with SANEXAS for neuropathy?
Neuropathy | Last Active: Jan 18 5:50pm | Replies (250)Comment receiving replies
New to Connect and don't really know how to use it, but hope this reaches you. Same diagnosis here : axonal multi sensory motor neuropathy. Frankly, I think that's all they do: diagnosis, since they have no idea how to treat it. My opinion is that if you live long enough, everybody gets some nerve damage because of the toxic environment of EMFs. We're bathing in a sea of nuclear waste. I've seen my last neurologist. Now I try any herbal, homeopathic and Ayurvedic treatment I can find. Rediscovered reflexology just now and will make it a part of my treatment. There is no cure, like Alzheimer's, just management, and struggling on. Good luck to all of us.....
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seanmacbeth - I know where you are coming from. I sort of felt the same way but then in the past few years I' ve revised my thinking. I've had PN for about 7 years, small amount prior to 2015-16 but that is when I got my first dx. My view is we need to allow these specialists to do tests, provide diagnosis, otherwise, there will be no cure. I feel the more the medical field learns about PN, the closer they will find the variety of triggers that likely cause this. I agree with you 100% about the toxic environment, damage done years back now surfacing later in life. DDT used to kill bugs in the 40's, 50's and 60's then found to be a toxin to humans and banned. Just an example. I find that if I lower my expectations of what I can do because of my PN, then do those things within my ability, I feel better. Also, still have not heard back from the company and my prior post. Hmmm. Best to all.