Has anyone benefited from treatment claimed by Neuropathy Clinics?

Hi Jeff @jeffrapp, No I think it's always appropriate to discuss claims made to see if they add up. I can only share my experience and tell you that I did a lot of research on my own and was taking most of the supplements already. I also learned that some of the supplements that I was taking were not high quality and some like the Alpha Lipoic Acid I was taking was mostly the synthetic inactive stuff and not doing the body any good. I do follow some of the older members in the group who were bedridden and found relief from all of their symptoms and were able to get off of the prescribed seizure medications for the neuropathy pain. I believe the controversy you are referring to is from the Facebook group Bob left because of issues with the current Admin. I was also a member in the other group and it was a neuropathy support group in name only. The person running that group created a bogus Ripoff Report that you can Google and get all the details including Bob's response and some comments by people that it has helped. He also shared a captured YouTube video of the guy that filed the bogus report. Ripoff Report is another dubious organization (IMHO) that lets any disgruntled person say whatever they want with no consequences and no way for you to clear your name if you are the target without thousands of dollars of legal fees.

That said, I know it may or may not help everyone even though it's helped me. I donate to the Help Another Member (H.A.M.) program when I am able. The program gives new members in need a one month supply to get them started and sometimes more than one month when possible. The H.A.M program is totally a members supported program and continues to help new members when funds are available. One negative comment I've heard over and over and can be viewed differently depending on your beliefs or frame of mind is if you join the Facebook group and don't read the introduction and start asking basic questions covered in the new member introduction without trying to search the group, the moderators have no patience and will tell you that they expect you to do your part and read and learn like everyone else. Tough but I can understand it and everyone needs to do their own research to avoid scams because they are out there.

Bottom line for me is that all of the supplements in the protocol are legit and have been identified by different research organizations/papers to help with neuropathy symptoms. The group had a page with links to all of the supplements on Amazon because of their 2 day delivery and availability. If you purchased the items using the links, Amazon gave a small percentage to the group like they do for any charitable organization and you can actually select which 501c3 you want to receive the percentage of each purchase you make and not use their links by searching for the same product. Now that they have the 525 product, the process is much simpler and less pills to swallow which benefits everyone on the protocol. I don't see that they make much profit if I was paying an average of <$10/day vs $6.44/day for the 525. I'm sure they are making a profit which part of goes to the member investors and the H.A.M. program which is OK by me, especially since the bottom line cost for me is the same between old and new.

John..read your 2020 post..I’m 83, 6’5”, 265 lbs diagnosed with non diabetic neuropathy last September. Started taking Alpha Lipoic Acid until I discovered a better purer source with no synthetic elements is R-Lipoic which I’ve been taking 600 mg a day for several months..in 2025 it’s hard to imagine the medical researchers have yet to discover medication etc to reduce progression etc ..I’m trying to increase exercise and have reduced sweets in my diet.. anything helping who knows..I wear compression socks…and just wish and hope it remains stable. How long have you have it? Thanks Bob

As a retired 73-year-old male whose 41 year career as a professional healthcare worker, I believe that I am qualified to answer this question.

I was diagnosed with “severe axonal sensorimotor polyneuropathy” during my treatment for stage four AML leukemia in 2012. During that time I have visited over a half a dozen so called neuropathy clinics throughout New England. One of those clinics was in the basement of a six story brick apartment house in New Hampshire. Every one of these clinics stated that they had extremely good results with their treatment of neuropathy.
I spent thousands of dollars seeking some sort of relief. I have included a link to the continuation of my story here. My advice is to stay away from those clinics.
https://connect.mayoclinic.org/comment/645606/
There is no universally recognized "true cure" for neuropathy. The effectiveness of treatments largely depends on addressing the underlying cause of the condition. In some cases, if the cause is identified and treated promptly, such as correcting vitamin deficiencies or managing diabetes, it may be possible to reverse or significantly improve neuropathy symptoms However, for many patients, neuropathy becomes a chronic condition requiring lifelong management of symptoms rather than a complete cure.

Personally, I got tremendous results with the RST Sanexas therapy.

For more information about my Sanexas treatments, and their locations, 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.
RSTSANEXAS.COM

Treatment Approaches
1. Addressing Underlying Causes: Managing conditions like diabetes or correcting vitamin deficiencies can help alleviate neuropathy symptoms
2. Medications: Various medications are used to manage symptoms, including pain relievers, antiseizure drugs (e.g., gabapentin, pregabalin), and certain antidepressants (e.g., duloxetine, nortriptyline) However, these treatments often involve trial and error, and their effectiveness varies among patients2.
3. Lifestyle Changes: Quitting smoking, exercising regularly, maintaining a healthy diet, and avoiding excessive alcohol can help manage symptoms and prevent further nerve damage.
4. Natural and Complementary Therapies: Options like acupuncture, alpha-lipoic acid, and certain amino acids may provide relief for some patients, though more research is needed to confirm their effectiveness.
5.
In summary, while some cases of neuropathy can be improved or reversed by addressing the underlying cause, there is no single "cure" for neuropathy. Treatment typically focuses on managing symptoms and preventing further nerve damage.

I have spoken to Ms Debbie Hansen.
The price of their equipment is about 50,000/* US dollars

Plz tell us what is the cost of 1 treatment.
I am it Delhi, India.
I appreciate your candid statement.
Dr Sunil Aggarwal DPT

You are correct, the machine does cost that much. However, the price of the treatment depends on the facility who is sets the price. I do know that here in the United States, the price varies from $75 up to $200 per treatment.

3 years ago I spent $7500 & traveled 110 miles one way 3 times a week to a clinic in Denver on South Broadway. They did red light therapy, stem cell injections in both feet & legs & electrical stimulation. I also bought a red light boot & a vibrating platform to use at home. It did not work. 1 year later this business went out of business. Be very cautious of spending a lot of money with no money back guarantee if it does not work.