LymeNet Flash: Don't think I posted this yet but a few weeks ago I found out I have sensory nerve

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»	LymeNet Flash » Questions and Discussion » Medical Questions » Don't think I posted this yet but a few weeks ago I found out I have sensory nerve

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Topic: Don't think I posted this yet but a few weeks ago I found out I have sensory nerve

BackinStOlaf
Frequent Contributor (1K+ posts)
Member # 23725

posted

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.

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First Symptom 9/09
Multiple docs, negative Labcorp test
LLMD: 1/10
Positive Igenex/CDC test
Treatment 2/10
2/10-8/10 Amox, ceftin, zith, flagyl
Currently: Bicillin, Minocycline, still dealing with severe breathing issues

Posts: 1121 | From New York, New York | Registered: Dec 2009 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

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.

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--Lymetutu--
Opinions, not medical advice!

Posts: 96223 | From Texas | Registered: Feb 2001 | IP: Logged |

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