Small Fiber Neuropathy
Are there any treatments available or trials for Small Fiber Neuropathy? My symptoms get worse every day. Thank you
Interested in more discussions like this? Go to the Neuropathy Support Group.
Are there any treatments available or trials for Small Fiber Neuropathy? My symptoms get worse every day. Thank you
Interested in more discussions like this? Go to the Neuropathy Support Group.
Thank you so much. I think I just deleted my comment. My hands are swollen. Would do appreciate hearing more and learning how to cope with these challenges. I don’t have another neurologist appointment until next week. Thank you again!
Hi, julbpat. Possibly I should not have used the word "pain." When I'm walking, I'll sometimes feel "discomfort," which may be due to a number of causes: (1) not the best-fitting shoes, (2) failure on my part to trim my toenails, pumice the rough patches, etc., or (3) a bunched-up sock. I believe my orthotics are well-fitted to my feet. But that's about it: "discomfort" (sometimes) when I'm walking, but not what I would call "pain." Most telling, in my mind, when I consider my PN, is having no foot pain when I'm at rest, either barefoot around the hose (as now) or when sleeping. That's why my podiatrist and I both feel that my periodic foot "ouches" are mundane and not related to my PN. Have you made any progress toward getting relief? –Ray
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1 ReactionDiscomfort is way better than pain! When my neuropathy is misbehaving, my feet, especially toes, burn. It feels like they are submerged in ice water. Freezing combined with burning. Fortunately I rarely experience that anymore on Tegretol, but it’s really hard to sit and relax, or sleep, when your toes are burning! Glad to hear yours is just normal foot aches.
The bunched up sock feeling is familiar with length dependent small fiber neuropathy. My family is used to my stopping and removing a shoe to rearrange a sock (that is not bunched up), or shake out a tiny rock or grain of sand. I wear sandals in the yard, and no grass or leaves can be between my feet and the shoe! Lots of stopping and rearranging!
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1 ReactionWhatever helps! I suppose it doesn't matter whether a person's foot discomfort (and now I'll use discomfort rather than pain) is PN-related or not – if you've learned techniques that provide some measure of relief, that's what really matters. Here's to a good – minimal foot discomfort – day! –Ray
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1 ReactionI also had a compounded cream ordered by my foot doc for the pain in my feet.
Mine consists of Lidocaine Gabapentin Pentox, Clon, and Amit.
I was to put it on 3x/day wherever the pain was on my feet.
After a week I broke out in a measles type rash on my feet, and had to stop using the cream.
I paid $84 for it, and it wasn’t covered by my insurance either.
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1 ReactionI’m afraid to try the tube he ordered for me. I’m not on many drugs for that reason.
It’s always interesting to me how many people think that small-fiber neuropathy is only the extremities because that’s the only kind that they’re aware of. Ugh.
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2 ReactionsI too had a compound med done for my feet but I broke out with a measles type rash after a few days using it.
My foot doc told me to discontinue it.
So far I'm doing well. It's only helping in my feet but it's still some relief. I'm sorry it caused you to develop a rash that makes it worse and I don't wish this pain on anyone.
Glad to hear it!