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@mlross4508

Thanks for your reply. This forum is helping me realize that I’m not alone. I’ve been too timid, for lack of a better word, to look in forums like these. It’s really beginning to help me as now I have resources that can offer alternatives and options I didn’t know were out there. My feet are in constant pain 24/7, even with my feet up in a recliner. The gab and oxy takes the edge off but I’m always in some amt of pain, anywhere from a 6 to an 8 on the pain scale.
Thanks for everyone’s support as well and thank you Carol.

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Replies to "Thanks for your reply. This forum is helping me realize that I’m not alone. I’ve been..."

@mlross4508 You are definitely not alone and don't feel that you can't ask questions and make comments. This site addresses issues on just about everything. I started as a patient and still am. I continue to have issues that I need someone to help me find answers for or read a post from someone who has the same problems. It is very comforting and definitely helps. We may never get the answer, but we all continue to search. Look at the numbers of people who have posted in the Neuropathy Group. There are many people who are dealing with this pain. We are all hoping for answers. So come in and ask, respond, rant and rave; Connect is the place where compassionate people will understand.
Carol

I took gabapentin, but side effects were almost worse than neuropathy. I have switched to Cymbalta....works a bit better , but less side effects.i do add a Lyrica sometimes when real bad. I did the electro therapy...useless. Useless.