Living with Neuropathy - Welcome to the group

@madgemgunia - Have you looked into or tried any complementary or alternative therapies to help with your neuropathy? Here are some ideas -- https://www.foundationforpn.org/living-well/integrative-therapies/

I thin k I have tried them all!!! I get comments from friends that had good results with alternative therapies and I am always hopeful but never have any positive results, but costs !!! I am still willing to try and I appreciate you message.!!!

Hello @jansendscards I have a different rare form of PN (CIDP) but many symptoms in common with numbness etc. However, I also experience very sharp shooting pain in arms & legs, seemingly out of nowhere, but happens often. Most Neurologists don't get the pain part... say that it is not part of PN. Clearly thousands of us disagree! Your ID of small cell will be helpful to many... thanks for sharing that.
As for MEDICATION: the only thing that helped with my radiating and shooting pain is Hydrocodone. With the entire "no opioids movement" I've been told countless times that this med. & Percocet are the same. They are not.... I have nerve pain constantly in teeth as well a (a different illness) and only hydrocodone will work, and works well... 10mg. I've had to give it up as I have severe chronic migraines as well... so was forced to choose for which pain I wanted relief; migraines = Percocet... nerve pain = Hydrocodone. Without Hydrocodone, I now have NO relief for NERVE pain. It can be torturous. I hope this is helpful. No one should have to live with this kind of pain... nor with choosing which pain one must suffer & one one with which to have help.
Also, I have not once had to increase dosage of Hydrocodone, (10+yrs) no tolerance build as is taken only when needed. Percocet for migraines was just the opposite. My wish is that someone in a position to do so will research this further. I certainly have.
I hope you find help soon. Very Best wishes to you.

Looking for specialist for small fiber neuropathy in Dallas TX. My husband is suffering without little improvement so I think we need to go back to correct diagnosis.

Hello @csc, Welcome to Connect. I'm sorry to hear your husband is suffering and not seeing much improvement. Here is one of the better sources of neuropathy information - Neuropathy Commons and it has a search function to look for a neurologist in your state. Here's the search link for Neuropathy Specialists in Texas - https://neuropathycommons.org/experts-directory/us?field_age_group_target_id%5B139%5D=139&field_state_target_id%5B336%5D=336

Are you able to share a little more about your husbands neuropathy symptoms and how long he's had them?

It seems to have started when he was put on statins 2 years ago.



I went to the Neuropathy Commons website, clicked on find a doctor for NV but zero names came up. Did I miss a step? Thank you.

@retired123 You didn't miss a step. Unfortunately Neuropathy Commons doesn't list any neurologists for Nevada. Not sure why unless they don't have any neurologists that have been associated with Neuropathy Commons. Here's a search listing for Nevada from U.S. News site -- https://health.usnews.com/doctors/neurologists/nevada

I thought I had small “cell” neuropathy but it is small “fiber.” What is the difference in these two?

I think they are the same thing. I've not heard the term small cell neuropathy but this may be what is meant but I'm not sure.

"What is another name for small fiber neuropathy? Small fiber sensory neuropathy (SFSN) is a disorder in which only the small sensory cutaneous nerves are affected." --- Small Fiber Sensory Neuropathy - Johns Hopkins Medicine: https://www.hopkinsmedicine.org/neurology_neurosurgery/centers_clinics/peripheral_nerve/conditions/small_fiber_sensory_neuropathy.html