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» LymeNet Flash » Questions and Discussion » Medical Questions » Motor Nerve Damage

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Author Topic: Motor Nerve Damage
kman543210
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Does anyone else here have motor nerve damage (not sensory nerves) caused by Lyme disease as seen by reinnervation and/or denervation in an EMG?
Posts: 20 | From Portland, OR | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
Tincup
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I do! I do!

Do I win a prize since I answered first?

[Big Grin]

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Posts: 20353 | From The Moon | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
CaliforniaLyme
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WELCOME!*)! to the board-
Many people do from Lyme-

People on this page did-

The ALS/Lyme Page
http://www.angelfire.com/planet/lymedisease/7/ALSLYME.html

Welcome again,
Best wishes,
Sarah

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There is no wealth but life.
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All truth goes through 3 stages: first it is ridiculed: then it is violently opposed: finally it is accepted as self evident. - Schopenhauer

Posts: 5639 | From Aptos CA USA | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
kman543210
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Tincup, what did your EMG show? Reinnervation and/or active denervation? How many limbs were involved and did you have swallowing and/or diaphragm involvement? Did treatment help these symptoms?
Posts: 20 | From Portland, OR | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
HaplyCarlessdave
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I had some trouble with swallowing at certain points with Lyme. I didn't have any kind of EMG or anything (no insurance), but that probably would have shown damage. I didn't take any supplements to directly affect nerve regeneration, but blood-thinning herbs such as Gingko were helpful, at least for sympton reduction.
The important thing is, all this stuff resolved after extended antibiotics and herbal treatment for Lyme and co-infections. Thus there was probably a certain amount of nerve regeneration happening.
Good luck; may you find the optimal treatment with the fewest possible setbacks!
DaveS

Posts: 4567 | From ithaca, NY, usa | Registered: Nov 2000  |  IP: Logged | Report this post to a Moderator
seewater69
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Hi!

I have a lot of problems that suggest irritation and damage of motor nerve, only my EMG that I took 2 yrs ago was perfectly normal (though I didn't have half the problems I have now) and all the drs I have seen recently tell me it is psycosomatic since emg is normal and will not repeat the emg because they don't think it is outdated. Don't quite know what to do, ah, before you ask, no, not a llmd in sight: you know I do live in Europe

Posts: 75 | From europe | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
djf2005
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kev-

i have not had the test/s you describe, but i did have all the sypmtoms you stated and to the same severity.

they resolved with extensive treatment with abx, hbot, sunlight, FIR sauna, detox, vit supp, and much more.

healing these diseases is an all day job for 2-4 yrs.

it sucks sometimes but look at it this way, when youre done, and healed, how much knowledge will you have gained?

hope you find the best treatment.

hang in there man

humbly

derek

--------------------
"Experience is not what happens to you; it is what you do with what happens to you."

[email protected]

Posts: 2269 | From Lansdowne, Pa | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
SouthernCO
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kman:

Had an EMG in 2002, 5 years before Lyme diagnosis, which showed L4 (or L5?) radiculopathy causing symptoms in both legs.

Posts: 175 | From Colorado | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
   

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