Does anybody have experience with SANEXAS for neuropathy?

And the answer to your question, I referred you to this link
https://www.rstsanexas.com/patient-resources/
Let me know if you have any further questions, and I will gladly answer them

Hello!

Has anyone tried Stemregen which are capsules that send stem cells from the bone marrow to the affected area such as my peripheral neuropathy?

The Rebuilder is a machine that involves EMS and TENS. Has anyone tired it?

Thanks!

Hi
I am in treatment now using the Sanexas, 7th treatment & I'm responding very well. I live in Phx area.

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!

I have had Sanexas treatment with injections and it helped,But after time i found the pain is back again with no relief,You have to find treatment that is best for you.I work everyday 7 days a week the doctors have told me to slow down a bit it might help the neuropathy pain.I am thinking stem cell treatments are next still doing research to see if it is safe for small fiber neuropathy. at this point i would drink rattle snake juice if it worked.

Hello Beverly,

Can you tell me more about your Sanexas treatments including costs and location?

Have you heard about the pill called Stemregen? It attracts bone marrow stem cells to damaged areas such as the nerves? It is expensive, but if it works, then I am eager for some resolution.

Thanks,
C E Harris
Sun City, AZ

I would be very happy to hear your story about Sanexas. I’ve had neuropathy for almost 8 yrs and I keep looking for some relief. I live in the Grand Rapids, MI area but I couldn’t find anyone who uses this. Thank you. I’d love to read your story. Thank you, Nancy Banks.

https://www.rstsanexas.com/patient-resources/

That’s great news! What is your diagnosis? I have a son with Small Fiber Neuropathy so I’m wondering if this would be appropriate for him? There’s no implant, correct?

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).