Hello @knucklehead4352 and welcome to Mayo Clinic Connect. I understand you are interested in hearing from members with experience with SANEXAS. I did a quick search on the site and found the following comments that you might find helpful by @erikas @dont
https://connect.mayoclinic.org/discussion/shingrix/?pg=17#comment-432255
https://connect.mayoclinic.org/discussion/just-diagnosed-2/?pg=10#comment-431976
Do you have PN and where did you come across information on SANEXAS, if I may ask?

I had the Sanexas treatment for 8 weeks. 3 times a week. It did nothing for me. A huge disappointment for sure. I’m still in terrible pain with extreme burning in my legs and feet. The guy giving treatment to me took an instant dislike to me for some reason so I never really trusted him and perhaps it showed. But I tried and hoped for the best. Sorry I’m not helpful to all my friends on here who share this evil condition. I pray for y’all and myself daily! God bless all of us. 🙏❤️🇺🇸

Hi @knucklehead4352 — I would like to add my welcome to Connect along with @amandajro and @momalin. I looked into a similar treatment but declined since it was expensive with no guarantees. And then there is this….from the Foundation for Peripheral Neuropathy:

Beware Expensive Treatments of Peripheral Neuropathy: https://www.foundationforpn.org/2016/04/11/5179/

@johnbishop These look similar to the kinds of mixed bag products you sent me.

?? Can you expand? I'm not sure what products you mean.

Yes, I have PN. Large add in the Desert Sun newspaper in Palm Springs, CA.