@crowhunter Unfortunately some things work for some and some don't. When I was diagnosed with idiopathic peripheral neuropathy a few years back my "so called" brilliant Neurologist provided no suggestions or options for treatment (That was the first and last time Visited him!).

What has helped me the most is (1) Mayo Clinic Connect and the numerous wonderful people who contribute to these discussions. I've received some wonderful options for temporary side effects that have helped me sleep with no burning or pain in my feet for example. I was pointed to a number of over the counter medications that I believe have been extremely helpful. I also have learned a lot on neuropathy from articles and studies recommended by members and group mentors. (2) From the beginning I have researched the subject on the "sites" of Mayo Clinic, Cleveland Clinic, MD Anderson and others (Specifically Neuropathy related research organizations, NIH etc.) and I continue to learn on a daily basis!

Let me add one more thing about Mayo Clinic Connect. I was diagnosed with prostate cancer 10-11 years ago - at the safe level (not aggressive) where I chose active surveillance since the diagnosis. This spring testing indicated I needed to address new findings (still contained in the prostate, so far). I have followed the various prostate related discussions and have learned so much from other individuals that it helped me and my wife choose the best medical option available to me at this stage of my life. In August I will have my procedure at Mayo Rochester. Mayo is one of the few in the country who has the medical device and individuals who perform this specific procedure. I would not have known about this procedure if I was not on the prostate cancer discussions because not one of the various "specialists" I met with ever brought it up as an option, not one. And you know why? It wasn't something they could offer....