EMG ON THE Pudendal Nerve

PNMLT, EMG, SSEP, and other Nerve function testing.
The different techniques, results and opinions.
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AAB
Posts: 5
Joined: Sat Apr 21, 2018 4:33 pm

EMG ON THE Pudendal Nerve

Post by AAB »

Has anyone had and EMG test on the pudendal nerve? I would like to know how it is done, does it hurt and does it leave lasting pain? Thank you in advance :-)
stephanies
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Joined: Mon Oct 25, 2010 3:07 am

Re: EMG ON THE Pudendal Nerve

Post by stephanies »

I had it done years ago. I did not know there were doctors still using this test. It was fairly painful for me and it caused an increase in pain for several weeks after the test.
PN started 2004 from fall. Surgery with Filler Nov. 2006, Dr. Campbell April 2007. Pain decreased by 85% in 2008 (rectal and sitting pain resolved completely), pain returned in 12/13. Pain reduced significantly beginning around 11/23.
AAB
Posts: 5
Joined: Sat Apr 21, 2018 4:33 pm

Re: EMG ON THE Pudendal Nerve

Post by AAB »

Thank you Stephanies for the information, I really appreciate it. They offered this to me at Stanford. They said it is all done externally with very small needles. Was yours also done externally? The test is not until August. I have been having second thoughts about having it done. I have had 2 doctors including Dr. Hibner and 1 PT tell me they think is the obturator spasms affecting the PN. I am seeing a Pelvic Pain specialist at Stanford and she seems like she wants to get to the root of this. She feels this test is one way to "rule out".
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Violet M
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Re: EMG ON THE Pudendal Nerve

Post by Violet M »

I had the pudendal nerve EMG. It was painful at the time but didn't last very long. I don't remember if there was much of a flare-up because I had surgery very soon afterward. The test did provide some valuable information in my case. Good luck if you have it. I would be interested to hear how it goes for you.

Violet
PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.
CALIhelp
Posts: 19
Joined: Fri Mar 06, 2020 2:14 am

Re: EMG ON THE Pudendal Nerve

Post by CALIhelp »

I had a EMG it hurts but not nearly as bad of having to deal with pudendal neuralgia
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