Hi all, I was wondering if any has had a Sprint PNS? If so, how did you do with it? My new Dr. gave me 3 options, 1) Sprint PNS, 2) LDN, 3) more blocks. I have had CRPS 1 for over 25 years. I just feel the LDN is a bandaid and I have done many blocks and it always comes back pretty strong after a few weeks. Reading about the Sprint PNS it sounds like even though it is a 60 day treatment, after they take it out I can stay pain free or have a better quality of life. I just feel that would be my better option. So just seeing if anyone has any experience with the Sprint PNS? Thanks for any input!
#eds#ComplexRegionalPainSyndrome #Gastroparesis #multipleTBI ’s