posted
I am having these recur after they've been gone for years. Came looking for suggestions but not finding much.
-------------------- Lyme by Igenex 8/2009. Sx of coinfections but no positive testing. Posts: 27 | From Seattle, WA | Registered: Jan 2010
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Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091
posted
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 . . .
Posts: 3771 | From around | Registered: Mar 2008
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posted
Anyone have suggestions on what can calm this down? I just started an herbal treatment and began having nerve pain.
Posts: 109 | From North East | Registered: Mar 2011
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