Re: Nerve Conduction Test/Pudendal Nerve

[Guest guest]

I am going to see the pudendal doctors in new

hampshire on sept 17-18 and i think they wanted to

have this test done....i am super freaked out now that

i read these posts....nne, did you have this test

done when you went to see Dr. Conway? Is it

absolutely necessary or should I just get the blocks?

Considering my pain is clitoral i am EXTREMELY nervous

that it will only make it worse because i heard they

shock somewhere around there.... :(

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[Guest guest]

Hollis,Do you have any other lyme symptoms besides vulvadynia? I'm assuming you have vulvadynia. Who diagnosed you with lyme disease?Zdamask@... wrote: In a message dated 8/31/2007 7:51:43 PM Eastern Daylight Time, cjenni (AT) suddenlink (DOT) net writes: Yes, i had one done many years ago on my leg. It was a horrendous experience -- more like torture -- and i could even imagine having it done for the pudendal nerve. Hollis Boy, i really screwed that up! What i meant to say is: i could NEVER imagine having it done on my pudendal nerve. I went into violent spasms and could not do the second part of the test. In my case, Lyme has totally disrupted my nervous system and it reacts in greatly magnified and very hypersensitive ways. Hollis

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[Guest guest]

Nerve conduction study is different from EMG. Nerve conduction

studies only last about 5 minutes unlike an EMG.

Kristy

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[Guest guest]

If you have a problem with systemic yeast (candidiasis), iti wouldn't

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