If you Google it you will find a list of medications that can exacerbate PN

Hi Caleb @highdesertdweller, Welcome to Connect. Sorry I missed your earlier post. You are not alone in your neuropathy journey. I shared my neuropathy journey in another discussion here - https://connect.mayoclinic.org/comment/310341/. I'm sorry to hear that you haven't found much relief yet. I'm glad you found Connect which also started my journey of learning as much as I can about neuropathy and what treatments might be helpful. You are your best advocate and learning as much as you can about neuropathy is key to finding something that will help.

Here are a couple of other discussions you might find helpful:
--- What helps the symptoms of Small Fiber Neuropathy?: https://connect.mayoclinic.org/discussion/tingling-from-small-fiber-neurapathy/
--- Small Fiber Neuropathy: What helps?: https://connect.mayoclinic.org/discussion/small-fiber-neuropathy/
--- Pins and needles plus vibrations SFN?: https://connect.mayoclinic.org/discussion/pins-and-needles-plus-vibrations-sfn/.

For learning more about neuropathy, here are my two go to websites:
--- Foundation for Peripheral Neuropathy: https://www.foundationforpn.org/living-well/
--- Neuropathy Commons: https://neuropathycommons.org/neuropathy/neuropathy-overview.

The Foundation for Peripheral Neuropathy also has a comprehensive list of complementary and alternative treatments you might find helpful - https://www.foundationforpn.org/wp-content/uploads/2020/08/Complementary-and-Alternative-Treatments-Revised-2020-final.-1.pdf

Do you mind sharing a little more about your neuropathy diagnosis?