← Return to Does anybody have experience with SANEXAS for neuropathy?

Discussion

Does anybody have experience with SANEXAS for neuropathy?

Neuropathy | Last Active: Jul 8 11:13pm | Replies (270)

Comment receiving replies
@swittstr

.. the link entered 1/6/21 above to www foundationforpn.org/2016/04/11/5179/ returns: "This page doesn't seem to exist." Searching for 'Sanexas' in their search box returns "Sorry, but nothing matched your search terms. Please try again with some different keywords."

Jump to this post


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.