Does anybody have experience with SANEXAS for neuropathy?

For more information about the Sanexas treatments, and to find the nearest Sanexas treatment center, You may call them at 702-315-2999 or 866-SANEXAS. (866-726-3927), and ask to talk to Debbie Hansen. Remember Everyone is different and treatment protocols may vary some due to their length of illness and damage to nerves. They are are there to help answer any your questions or concerns. Please let them know that I gave you this information so that your questions will be answered promptly. For the record, I have never been employed nor am I receiving any financial compensation from Sanexas. Wishing you all the very best for the upcoming holiday season.

I participated in a Sanexas trial a year ago. It was run by the neurology group I go to. Twice a week for 12 weeks. First, two bad car accidents, brain injury, and multiple spine, shoulder, elbow, knee and abdominal surgeries, pain, numbness, tingling, etc. Fused L3-S1 and C3-C7. Arachnoid adhesions present at L4-5. Progressive muscle spasms, pain, hot/cold, numbness with nearly no sensation in feet. So, bad, and no known successful treatment for arachnoiditis. Just narcotics and hope we don't kill ourselves. Went into trial not expecting any results but spasms stopped completely three weeks into treatment. End of 12 weeks had about 80% improvement in symptoms, but the most measurable result was going from four 10/325 oxycodone/day to two 5/325. Ended trial early January last year. Results held until June, so almost 6 months. Gradual decline since to about 60% of where I was when I started treatment. I'm told there were similar results for 60-70% of participants. Way better than anyone thought. Four patients at a time in the room where treatments were received (feet and calf only) so we were all able to talk freely. Reported results were consistent with conversations. (Just FYI, there was one fellow who had a poisoning situation from being a geologist in the mining industry. One foot amputated, the other half amputated. After about 3 weeks all the burning in his lower extremities stopped. After 10 weeks no more pain meds.) For some people this works, though I still don't really understand why. Extensive conversation with Medicare about the fact it is only approved with them and FDA under a physical therapy treatment code. So, cash only where it can be found and not one single physical therapy outfit in Colorado has even heard of it! Even the spinal cord injury experts at Craig Hospital in Denver. It obviously works for some people. Finding it is the problem. Considering moving to Florida so if Mayo is doing it I am interested. Hope this helps someone out there!

Tried 19 treatments did not experience any improvement.

Ccm

I am curious as to the time duration for your 19 treatments. Were those done in over weeks, or over a span of how many months. The reason I ask is it took me over 15 treatments over five months before I started seeing improvement

Hi Chaz, I haven’t tried Sanaxes as I hear it is not available in Colorado. But I have freezing cold feet from Neuropathy and what has really helped me has been wool felt shoe insoles from Amazon, Cozy Winters foot of the bed heating pad which is long and stays warm most of the night on a low setting and #1 Rock Dove Nomad slippers which are my go to when I’m indoors. I also use hot hands toe warmers in my shoes went outdoors along with the wool felt insoles. Maybe these will help you. Wishing you warm feet! Bcool

I just saw online that they are doing SANEXAS Treatments at Colorado Springs Neuro Associates. I’m going to check about Medicare coverage. Maybe it’s possible here in Colorado! Bcool

Got medicare coverage in VA.

I did 19 treatments with the Sanexas machine FDA approved did nothing for the nerve pain usually used for muscular type pain.

Yes 19 treatments FDA approved did nothing for me!