This is topic Don't think I posted this yet but a few weeks ago I found out I have sensory nerve in forum Medical Questions at LymeNet Flash.


To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/1/100310

Posted by BackinStOlaf (Member # 23725) on :
 
damage in my legs and arms. My sensory nerves do not respond to stimuli there. This is why I have had tingling all this time. I had an EMG test done. It seems to be getting worse, not better. The neurologist thinks I don�t have Lyme anymore (of course) but he thinks it could have been caused by the Lyme and that it might eventually regenerate but will take a very long time. I am so torn if I should go back on meds. (been off for about 7 weeks). I feel better off of them then on them. I am so confused.
 
Posted by Lymetoo (Member # 743) on :
 
I wondered what "sensory nerve" was .. finally had to open this to see!

You have to ask yourself what caused it. And the fact that it is getting worse would make me continue treatment.

Abx will make you feel worse. That's a fact. But that is the only way to get well unless you go to alternatives.
 


Powered by UBB.classic™ 6.7.3