I’m glad you’re given it as an option for possible hope of relief or improvement? That is, only if there are reasonable assurances along with little risk of adverse affects and it is affordable. I actually inquired about it as I was willing to try “anything” but my doctor flat out said that he was unable to prescribe it for my type of PN. I think that now that you’re given a choice, you are being very wise in reaching out to folks here who have actual experience in receiving the treatment. I hope you’ll share your experience. A question I have for you / is your doctor now saying you have BOTH SFN and Axonal Sensorimotor Neuropathy, the latter of which was confirmed by EMG? How did they make the original diagnosis of SFN?