Thread: Burning hands?
View Single Post
Old 04-25-2007, 07:25 AM
Kathi49 Kathi49 is offline
Member
 
Join Date: Sep 2006
Posts: 519
15 yr Member
Kathi49 Kathi49 is offline
Member
 
Join Date: Sep 2006
Posts: 519
15 yr Member
Default

Glenn,

I am just adding that my burning hands and feet began AFTER the first fusion I had. I just wonder if freeing up the nerves had something to do with it after a long time of compression. But at the same time the C5/C6 was still bad. After the second fusion it stopped altogether in my hands but it took a few months.

I do have a question though. It is still in my feet. I do have lumbar radiculopathy. The odd thing is no anti-convulsant meds touched the PN in my feet with the exception of Klonopin...it was the only med that helped. And now I am finding that Voltaren makes it almost go completely away! Okay for my question. Isn't PN supposed to "wrap around" completely as in a stocking? Because mine doesn't. It is always just on my outer ankle and foot; worst being the left side. So, I am going to assume it may be more radiculopathy. And, yep, have had thorough and complete tests. The small fiber stuff was supposedly so minute it almost didn't show up.
Kathi49 is offline   Reply With QuoteReply With Quote