Looking to connect with people who have non-diabetic neuropathy
Would. Like to find people with this issue
Interested in more discussions like this? Go to the Neuropathy Support Group.
Would. Like to find people with this issue
Interested in more discussions like this? Go to the Neuropathy Support Group.
I’ve not heard of it but will check it out. Thanks!
i have tryed it no help for me good luck but it keeps getting little worse all the time.
I have non diabetic neuropathy from cerebellar ataxia. Gabapentin helps some
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3 ReactionsI am very new to Mayo and this conversation but I am surprised to read this. I have trigeminal-mandibular neuropathy and occipital neuralgia (interchangeable with neuropathy depending on who is talking). I have been treated for migraines for years and my pain dr made the diagnosis change after a detailed visit last year. I have received several occipital nerve blocks, lasting about 6-10 weeks each and cut back on migraine meds.
My first visit at Mayo-Jacksonville was April 5, specifically for my facial pain, but my appointment was with Dr Fermo, a Neurologist, that specializes in Botox treatment for head neuropathy.
It might be worth a phone call, visit or virtual visit.
Hope you find help.
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2 Reactions@mvanstem
Is your ataxia occasional or constant? Would you mind sharing your ataxia symptoms?
Thank you,
Jake
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2 ReactionsAtaxia gait, lousy balance, nystagmus,occasional vertigo
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1 ReactionI have MGUS and few years ago I started having neuropathy in my feet then the nerve problem is now over my entire body. I am not telling anyone what to do. I couldn’t get any pain pills for the problem so I took a chance and tried using marijuana and it seems to help. I also take 800 mg three times a day of gabapentin. I don’t know if it works or not. I am in my late 70’s and have these health problems. Every other day or so I have nerve attacks over my entire body that will last all day. I wish you well and hope you get better.
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2 ReactionsWelcome @luckyride, Thanks for sharing what helps you. Since you mentioned MGUS, I thought you might also find the following discussion helpful:
--- Does anyone have neuropathy related to MGUS?: https://connect.mayoclinic.org/discussion/mgus-neuropathy/.
Have you tried any other complementary or alternative treatments to see if they help with the neuropathy and nerve problems?
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1 ReactionI have asked my MGUS doctor and he said he can’t help me with my neuropathy or nerve problems and I have been to several neurologist doctors and same answer and I might ad been to several pain doctors and no help. So far I have not found any other treatments.
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2 ReactionsThe Foundation for Peripheral Neuropathy has a list of complementary and alternative treatments you might find helpful here - https://www.foundationforpn.org/living-well/complementary-therapies/.
Also, there are some other neuropathy discussions you might find helpful:
--- Small Fiber Neuropathy: What helps?: https://connect.mayoclinic.org/discussion/small-fiber-neuropathy/
--- Member Neuropathy Journey Stories: What's Yours?: https://connect.mayoclinic.org/discussion/member-neuoropathy-journey-stories-whats-yours/
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3 Reactions