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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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@drtypws

I'm glad it helped you.
Where I went for my treatments the injections weren't an option. I had to get them. After 14 treatments, I had a bad reaction to the injections. They said I couldn't continue the treatments without the injections. The treatments were helping me and I wanted to continue but they said no.

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Replies to "I'm glad it helped you. Where I went for my treatments the injections weren't an option...."

So sorry to hear what was going on. What area do you live in?
One time I tried the treatment without the injections, just to see what the difference was & I feel the treatment without the injection was a waste of time. I felt nothing, not any improvement. I competed my 24 treatments with the injections & I am very happy with the outcome. Is it completely gone....NO but it is very manageable & I feel almost new.

I had the Sanexas treatment last year with the injections. They did not seem to work for me after two months. I got a blood panel of vitamin/minerals because I suspected an overdose of B6 and/or B12 since I was taking supplements at the time of the treatments. Discovered to my amazement that I had a serious overdose of B6, which I have since learned can make symptoms worse. So after talking to Sanexis, they have offered to help with my clinic to place the electrodes a bit differently and I will reduce my intake of supplemental B6 and have blood taken more frequently to minimize the risk of overdose. They also use ALA in the injection, which I also take daily as a supplement, with Acetyl-L-Carnitine. I have been self-treating since the onset of symptoms in 2018. Never taken any of the traditional Rx meds. Everything is in nutrition for me. Even started this year adding dandelion greens to my regimen! Seem to be keeping this at bay for now while ever searching for new foods and supplements. Nature gave us this and nature can cure it...... Watch for overdose of B6.