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Anyone found help?
Just found Out I have neuropathy. Need those who want to share their experience with this disease!
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Just found Out I have neuropathy. Need those who want to share their experience with this disease!
Interested in more discussions like this? Go to the Neuropathy Support Group.
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Hello Pattileigh @leighsingley7, Welcome to Connect. I shared my neuropathy journey in another discussion here - https://connect.mayoclinic.org/comment/310341/. Sorry to hear that you have joined our club. The best thing you can do to help yourself is learn as much as you can about neuropathy. You are not alone and there is a lot of experience here on Connect. Here's a list of the discussions where folks are discussing "neuropathy what helps" - https://connect.mayoclinic.org/search/.
If you haven't seen the Foundation for Peripheral Neuropathy website it has a lot of tips and suggestions to help you through your journey with this condition - https://www.foundationforpn.org/living-well/. They also have a YouTube Channel where they have all of their past webinars for different neuropathy topics - https://www.youtube.com/@foundationforperipheralneu4122.
You mentioned you just found out you have neuropathy. Do you mind sharing a little more about your diagnosis and what symptoms you have?
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4 ReactionsNothing has helped me. getting worse over time. any advice to stop the spread?
How did you learn that you have neuropathy? Do you know the cause of your neuropathy? You might want to get an EMG test from a neurologist to see what, if any, kind of nerve damage you have. Try to stay positive. My neuropathy is not painful and I take vitamin supplements to help rebuild nerves and sustain my health. I wish you the best.