Does anybody have experience with SANEXAS for neuropathy?

Hi @beardog, Thanks for sharing that Sanexas treatments helped. Do you mind sharing a little more about your neuropathy diagnosis and how long you have had it?

Hi mentor,I’ve had neuropathy for over 12 years.the doctor did a biopsy on my legs,they said a normal nerve in your legs was 4.0. Mine was 0.03 in both legs.so that told them that it was neuropathy.also neuropathy was the reason I retired early,I couldn’t take standing on concrete anymore it was just to painful.I was watching tv and I saw a commercial about sanextas,so I tried it what did I have to lose,I’ve tried everything else.after the first 4 treatments I could tell it was helping,I took a total of 14 treatments.after the treatments my feet and legs felt great. I could walk better and I could stand longer than I had for the past 12 years. I know it’s not going to work for everyone but it worked for me.

That's great to hear!

Same experience here: tried for three months TENS treatment.. Nothing. Began to think it was just another scam. Then I discovered Sanexas, said to be stronger, more effective treatment but can't find anyone local .

Where are you located…?

Richmond area. Found National Neuropathy Center. They use the Sanexas machine NeoGen.

Every year since I was born, my birthday was a special day for me. As a child, and as I grew to be 60 years old, it was always my special day off!  No school and no work!
However, on my 61st birthday, what started out as my special day, turned into the realization that my 41 year career as a professional health care administrator was over and my next career would be as a “professional patient.”  

I was diagnosed by my oncologist with severe AML leukemia and that “there was a bed waiting for me 90 miles away in Boston, Massachusetts.” I was heading toward the most challenging journey of my life. Within a month later, following the first round of chemotherapy, I was found unconscious, coded, suffering severe neurological defects, a permanently detached left eye retina, and was placed on a ventilator for three days. It would take another two months in a Rehabilitation Center for me to get home with an expiration date of less than six months, which by the way was extended twice!

I finally arrived home, 3 months later in an ambulance and dumped in my bed.  I found myself wearing diapers, a feeding tube inserted in my stomach, taking 16 different medications, and needing 24/7 care.  My arms and legs were totally useless.  To be honest, I knew that I was heading towards the end of the line and I couldn’t wait to get there.  I had visiting nurses, home health aides, therapists, clinicians, social workers checking up on me daily, and the list went on and on. During the year 2013, I was rushed to the hospital eight times. I was encouraged to go to hospice several times, however, I figured if I was going to check out, I was going to check out in my home!

Fast forward 2 1/2 years later of being bedridden and the doctors, who were sure the leukemia would come back, were all wondering why it didn’t!  

Please see the video. https://youtu.be/WUL-q2t_tZQ

So now it’s ten months since my daughter's wedding video went viral. During that time I continued to be in and out of hospitals and rehab facilities and tried all kinds of different medications with their usual side effects.  I finally got to see the top neurologist in my area in July 2016, and after having all kinds of lab tests, x-rays, and an EMG, I finally got a formal diagnosis called “severe axonal sensorimotor polyneuropathy.”  If you ever have had  Novocaine for dental work, imagine your whole body feeling that way permanently!  She also informed me that “there was no cure, just medication for the numerous symptoms, but I would have to live the rest of my life with it.”  The neuropathy affected my balance, my ability to feel anything, and the whole experience left me with off and on tremors. I was falling at least twice a month.  I needed help entering and leaving a car.  My family purchased a wheelchair adaptable van that could carry my battery powered wheelchair because of the need to use a wheelchair in open spaces.

From that point forward, it was just me and my iPad. Every day while lying in my bed I would search the Internet for all of the information about my neuropathy. I found several clinics throughout the United States that offered life changing stem cell therapy or medications for my condition. I would spend hours each day talking on the phone to different clinics, hospitals, doctors offices throughout the country.  I sent countless copies of my medical records out to these places in hopes that someone could help me. I even went to see a doctor whose practice was in a dark windowless basement of a commercial building in New Hampshire, but he only takes cash!  Now that’s not fishy at all!  I tried different drugs, gabapentin, B12, celexa, Nortriptyline, Lyrica and also several over-the-counter neuropathy drugs.  Nothing worked, and the side effects were unbearable. I even tried acupuncture during the summer, the side effect?, I slept through them!

Since I am not able to hold a newspaper, I read the local paper on my iPad, and one day in January, 2021, I spotted a small ad from a brand new business in WIndham, Maine called Nulife Wellness, that appeared to be a letter written just for me and my condition. I hurriedly called the phone number and made an appointment with Sara Doyon, a family nurse practitioner, to schedule a half hour treatment from a machine that looked like a big TENS unit, but it was much more than that! A TENS machine is like a X-ray and RST SANEXAS neoGEN device is like getting a MRI. More powerful frequencies and over 20 different treatment programs designed for acute and chronic painful conditions.

It had lots of electrodes that sent electrical impulses through the skin with the goal of regrowing nerves.  It was not at all painful, just a soothing electrical massage to my legs, however the cold and snow of winter delayed my continuation of treatments.

I restarted treatments by going twice a week through March and April.  During that time I experienced no results.  I was desperate and began to think that nothing could help me, and that it was time to permanently discontinue them. On the last Thursday of April, I went home thinking that this would be my last treatment.

I had made my decision that night when I awoke the following morning I would call and cancel further treatments.  That night while asleep following a day treatment I was awakened by the extreme discomfort and heaviness of both my legs. My legs felt like I had run a 26 mile marathon. It was then that I realized why they felt that way.  I was experiencing nerve regrowth!  The treatment finally woke up my legs!  I was actually feeling pain for the first time in 8 years!  As much as they hurt real bad, I knew why! It was at that point that I realized I was on to something. In the morning I called Sara and told her the good news, and I continued my treatments with her right through the month of June.  

Due to the fact that I was showing signs of significant improvement, Sara called the company that manufactures the machine to let them know how well I was progressing.  The name of the company is RST-SENAXAS which is located in Las Vegas. In July, I decided to make a few appointments for further treatments with them during the middle of August. Since then, there have been several more improvements in my regaining mobility.  

As I write this, it’s been SIX months since my last fall!

I have suffered with polyneuropathy for 9 years and (I've been) trying to be more independent.  I want to make it real clear that this machine is by far the best treatment I have undertaken that reduces the symptoms of absolute stiffness and increases sensations in my limbs.  It is not yet a cure, but a real treatment!  We have to keep in mind though, nerve regrowth is a process that does not occur overnight, it takes time! With me it took over 15 treatments over a 4 month period before experiencing the positive result.

The second video was after Sanexas taken this summer of me trying to run.

Amazing story. I start treatments next week. Want to catch this early before it gets worse. So far, no pain. Not linked to diabetes. Every test shows normal glucose levels, A1C under 5. Vegetarian diet. Balance is the main issue. I try everything but Rx meds. Latest discovery: reflexology. Had two treatments so far and find noticeable improvement. Exercise and movement is key to managing this condition. And sharing notes among others with this strange disorder.

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.

Starting Sanexas treatment 12/5. Will try anything. Just diagnosed with Axonal Mixed Sensory Motor Neuropathy. At least it has a name now. There is so much misinformation and misdiagnosis out there. No pain, just tingling and numbness in feet and lower leg. Feels like I imagine frostbite would be. I take only supplements for it: ayurvedic, tcm and naturopathic, no Rx. Vegetarian diet. Major issue: balance and foggy brain.