This is topic parathesia in forum Medical Questions at LymeNet Flash.

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Posted by marie (Member # 3980) on :
Anyone else have this? What is helping you.
Posted by dex3703 (Member # 23930) on :
I am having these recur after they've been gone for years. Came looking for suggestions but not finding much.
Posted by Rumigirl (Member # 15091) on :
A word of warning from my own hard experience: paresthesias can be from Lyme, or possibly a co-infection. I suggest seeing your LLMD promptly and stick with treatment. If you don't have one now, please seek a good one. Please don't wait.

Without prompt and sustained treatment, the paresthesias can build into full-blown terribly painful nerve damage. I'm not saying that it will, but it can over time.

I experienced these, but did not get help from my LLMD or a LL neurologist promptly enough, due to being overwhelmed with pretty much everything going wrong at once and being horribly debilitated.

I now have full-blown horrifically painful wide-spread nerve damage. I wouldn't wish it on anyone. My situation has too many factors going on, but . . .
Posted by Lassie27 (Member # 31083) on :
Anyone have suggestions on what can calm this down? I just started an herbal treatment and began having nerve pain.

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