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You might find these other discussions helpful also:
-- Small Fiber Neuropathy: What helps?: https://connect.mayoclinic.org/discussion/small-fiber-neuropathy/
-- Small Fiber Neuropathy burning?: https://connect.mayoclinic.org/discussion/small-fiber-neuropathy-burning/
-- Member Neuropathy Journey Stories: What's Yours?: https://connect.mayoclinic.org/discussion/member-neuoropathy-journey-stories-whats-yours/
One of the things that has helped me was to learn as much as I can about neuropathy, it's symptoms and available treatments. Two sites that I've found really useful:
-- Foundation for Peripheral Neuropathy: https://www.foundationforpn.org/
-- Neuropathy Commons: https://neuropathycommons.org/neuropathy/neuropathy-overview
The Foundation for Peripheral Neuropathy has a good list of Complementary and Alternative Treatments that you may find helpful -- https://www.foundationforpn.org/wp-content/uploads/2020/08/Complementary-and-Alternative-Treatments-Revised-2020-final.-1.pdf
Replies to "You might find these other discussions helpful also: -- Small Fiber Neuropathy: What helps?: https://connect.mayoclinic.org/discussion/small-fiber-neuropathy/ --..."
Connect
As I read through the experiences of folks on this Connect site, I see a few references to diet but have yet to find anything definitive. Has anyone found a great resource that connects diet with neuropathy symptoms?
I recently read a phrase that is new to me, “Neuro excitable foods.” I’ll begins searching in this phrase, but I would love to hear your thoughts and know your resources. Thank you.