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DiscussionDoes anybody have experience with SANEXAS for neuropathy?
Neuropathy | Last Active: Jul 8 11:13pm | Replies (270)Comment receiving replies
Replies to ".. the link entered 1/6/21 above to www foundationforpn.org/2016/04/11/5179/ returns: "This page doesn't seem to exist."..."
Hello @swittstr - I updated the link on the referrenced page. It looks like they updated their website awhile back and moved things around and placed it into their eCatalog here - https://myemail.constantcontact.com/FPN-E-Tips---March-20---Buyer-beware-.html?soid=1102887337862&aid=HRBlZ67oHBg
The good news is that they have made it easier to find information all in one place here: https://www.foundationforpn.org/wp-content/uploads/2021/12/11.23.2021-Website-eCatalog.pdf
In retrospect, I shared that I looked into a similar treatment (not Sanexas) and declined it because of the cost and I didn't think it would help me. @duquer shared his story of how it helped him here - https://connect.mayoclinic.org/comment/645606/. I replied to his post and shared a video for him of his story. Hope this helps. Sorry for the broken link.