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← Return to Small fiber neuropathy?
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There are so many paths the various Neuropathies take. For me, my desire to get as much specific information on the exact type or possible reasons is to help connect most with people are on the most similar path as my own. This perhaps helps me prioritize things to try to help me stabilize and improve my mobility. There are so many different symptoms and so many things to try, I like narrowing down the list by borrowing from the successes others have already had and try those ideas first. I also like borrowing from others most like me on what things I might want to avoid.
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what you said makes perfect sense. I didn’t know before reading your post there are different varieties of neuropathy. That is probably why it is confusing. Feel better.
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Debbie - You hit the nail on the head....again. Like you, I've tried to learn from others involved in Connect what might work, what might not in coping with PN. I have given a lot of thought lately as to the various symptoms we hear about on Connect and who knows how many unknown causes. No wonder PN is a mystery. I've had 3 docs give me 3 different possible causes for PN. Mayo said we don't know, and I have decided to live with their diagnosis. Keep learning and keep moving. For now, it's the best we can do. Ed