Does anybody have experience with SANEXAS for neuropathy?

Posted by knucklehead4352 @knucklehead4352, Jan 6, 2021

Does anybody have experience with SANEXAS. It is touted as Electric Cell Signaling Treatment especially for peripheral neuropathy.

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@bevely

Your best bet is to go on the Internet & look up Small Fiber Neuropathy and also the Sanexas .
I have Peripheral neuropathy & I am under the care of a place in Peoria that uses the Sanexas & they use shots with their treatments. I am very ok with the shots, as they are only injectable blends of vits & mineral.
I do not want to take drugs or do surgery. I will complete the treatments & later on in life, if it starts to come back, I would do follow up treatments.
So, please research. There is a lot of information out there & also lots of info that says, "you have to live with it."
NOT ME I got to feel the "fur" on the sole of my slipper the other day & it was great. I haven't had that feeling for years (foot numb).

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Are your treatments covered medicare? Do you know the cost. Are you in Peoria Illinois or some other state. I'm in Arkansas and have not found this treatment available near me.

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Yes, my medicare does cover their part & my supplement insurance covers the rest, and no, I do not know the cost. I was just to happy, they covered the 24 treatments required.
I am in Phoenix, AZ & Peoria is just were I go for treatments.

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@bevely

Yes, my medicare does cover their part & my supplement insurance covers the rest, and no, I do not know the cost. I was just to happy, they covered the 24 treatments required.
I am in Phoenix, AZ & Peoria is just were I go for treatments.

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I looked up a place on the internet in AR. Bentonville, AR 479 367-4589 , I'm not sure if this city is near you but you could call them to get more information

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@duquer

I just wanted to share with you, that I also have had a lot of symptoms of neuropathy numbness and pain. My diagnosis is severe axonal sensorimotor polyneuropathy. It took me six years to find a Sanexas treatment here in Maine that actually really works! If you would like to know more about the revolutionary Sanexas treatments, without the injections. I would gladly send you my story. Let me know. Wish you the best!

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I sure would like to know more about Sanexas treatment as I am miserable with neuropathy constantly.....Would be great to find something that works!!!!!

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@madgemgunia

I sure would like to know more about Sanexas treatment as I am miserable with neuropathy constantly.....Would be great to find something that works!!!!!

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https://www.rstsanexas.com/patient-resources/
Scroll down to read my story
Please help me a lot.
My name is Ralph

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@bevely

I looked up a place on the internet in AR. Bentonville, AR 479 367-4589 , I'm not sure if this city is near you but you could call them to get more information

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It's about 4 hours away but I will call them to see if they know of treatment in my area. Thanks!!

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@madgemgunia

I sure would like to know more about Sanexas treatment as I am miserable with neuropathy constantly.....Would be great to find something that works!!!!!

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There is lots of information out there, you will just have to let your fingers do the typing (researh) LOL That's how I found out about Sanexas. I wasn't going to live with "nothing can be done" attitude and also, places where helping others but WON'T have anything to do with you because of your insurance! Crap.....
So, I got my feathers in a knot & went on a hunt to do something that is natural & fairly easy on my body. It is working & I am so thankful I didn't give up. I even went back to yoga, (basics ) for now to help the process along to strengthen my muscles. Again, I didn't give up. I am 75 yrs young & want to live a good life without pain.
I hope you can look more into the Sanexas treatment for yourself. Good luck

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@bevely

There is lots of information out there, you will just have to let your fingers do the typing (researh) LOL That's how I found out about Sanexas. I wasn't going to live with "nothing can be done" attitude and also, places where helping others but WON'T have anything to do with you because of your insurance! Crap.....
So, I got my feathers in a knot & went on a hunt to do something that is natural & fairly easy on my body. It is working & I am so thankful I didn't give up. I even went back to yoga, (basics ) for now to help the process along to strengthen my muscles. Again, I didn't give up. I am 75 yrs young & want to live a good life without pain.
I hope you can look more into the Sanexas treatment for yourself. Good luck

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Yes I am certainly not giving up. Except for this numbness in feet that has progressed over 5-6 years to ankles and shins but no pain I feel great at 69. I had to visit nursing home recently and seeing all those struggling to walk has made me even more determine to find answer. Sadly this treatment is not available anywhere within 4-6 hours of me and can't see how I could get that many treatments that far away. Also this is first treatment I have heard of that medicare may actually cover. I take no medication and not interested in any. Can't understand why this is not more widely available if medicare covers that cost.

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Not many Dr's out there work with the integrated approach to medical treatment to help you regain control of the pain (some chronic) . They can only give drugs & big pharma loves that. I don't want to go any further into that subject. I think we all get the picture.
The Sanexas, treats the root cause of the disease process & I'm all for that. I think it's only been around since 2000 or later & I think it's starting to catch on by referral from a Neurologist. My neurologist knows I will not do DRUGS & I told him, "there must be something else I can do to stop this." He then gave me a print out from his computer about the Sanexas treatments & told me, he thought I'd be a good candiate. So I did & it's working great. I to could not do 3 X week, so I do 2 a week.
There are not enought (real) Integrated Health provides out there, so the treatment is slow off the ground & a lot of insurances do not cover, integrated medicine. That's sad to say.
I hope something comes your way.

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