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

Discussion

Does anybody have experience with SANEXAS for neuropathy?

Neuropathy | Last Active: May 17 11:36am | Replies (267)

Comment receiving replies
@johnbishop

Hello @jzxbb, Welcome to Connect. I know it must be difficult managing the pain. I'm sorry to hear that the Sanexas treatments didn't provide any relief. I'm not sure if you are aware of the Foundation for Peripheral Neropathy but their site may provide some helpful suggestions here - https://www.foundationforpn.org/living-well/.

You mentioned chronic undiagnosed pain with peripheral neuropathy. Have you thought about seeking help at a teaching hospital or major health facility like Mayo Clinic?

Jump to this post


Replies to "Hello @jzxbb, Welcome to Connect. I know it must be difficult managing the pain. I'm sorry..."

Thanks for your consideration.
I've seen in about 45 years almost 250 Doctors in the NE with no luck including Hopkins, U of MD and Hershey but this is totally weird.
Considering how long it's lasted and how extreme it is I'm sure the Sanexas had no part in it but who knows. Frankly I can barely walk or drive so everything is done for me now. Thanks a lot anyways but my life is over now. 250!!!!!! cmon!