← Return to Foot neuropathy: What gives you relief?

Discussion

Foot neuropathy: What gives you relief?

Neuropathy | Last Active: Sep 8 4:08am | Replies (418)
Comment receiving replies
@preknight

I went to a neurologist that was associated with Neuropathy Association, and he was of no help either. All I ever hear is "There is no cure for neuropathy." The neurologist that I now go to just checks to see what progress the neuropathy is making, i.e., how strong my grip is, how far up I have feeling on my legs, etc. Hang in there.

Jump to this post

Replies to "I went to a neurologist that was associated with Neuropathy Association, and he was of no..."
Evie | @archermac15 | May 10, 2022

For me the worst part is the Restless legs. For most people it's just at night, but when I got the Neuropathy in my hands and feet, that's when the RLS started off and on in January, by February it was constant and I had to get the Lyrica from my pain Doctor my Neurologist didn't even prescribe it. He sent me for labwork to check my Iron, and I went to the lab in pain only to find out that he forgot to put down the test they check for Iron so I had to go again. It turned out that my iron levels were good, but he prescribed Iron anyway. I've heard and read that it's not good to take Iron if your levels are good.

VIEW AND REPLY