PN or Levator Ani Syndrome

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LindafromNJ
Posts: 9
Joined: Fri May 26, 2017 12:38 am

PN or Levator Ani Syndrome

Post by LindafromNJ »

Hi new to site. Have not been diagnosed with PN as of yet. Going to my gynecologist this week. I am being treated for vaginal atrophy which may have improved a little. However I have the burning and itching vagina inside and now developed anal pain. It seems like it is a muscle pain on the left side and it hurts. The vagina pain is on the left. Got an exam from gastro doctor who said he felt no lumps. He gave me steroid suppositories. I think I may have Levator Ani Syndrome. Can you have that and PN. Another odd thing is when I have my vaginal pain the anal pain goes away and vice versa. In addition sitting aggravates both. Any insight is helpful. I think the worst is not knowing what you have.
janetm2
Posts: 987
Joined: Sun Jun 12, 2011 10:54 pm
Location: Maryland

Re: PN or Levator Ani Syndrome

Post by janetm2 »

Hi Linda,
I first had levitor Ani muscle spasms (gastroenterologist sent me to colon rectal surgeon that diagnosed it). They did electro-Galvanic stimulation (EGS) treatments to stop it. warm baths also helped​. I had it the next year as well. Then a couple years later I had PNE, the EGS and Botox didn't help and I went to PT then Dr Marvel to diagnose PNE. Went on to decompression surgery and now have residual PN. I can say the pain seems the same, so really hard to say which was witch without the professionals or if there was an overlap. I hope you can pinpoint the problem and get some treatments to alleviate the pain.
Janet
2007-08 pelvic muscles spasms treated by EGS. 6/27/10 sat too long on hard chair- spasms, EGS not work Botox help, cortisone shots in coccyx help, still pain, PT found PNE & sent me to Dr Marvel nerve blocks & MRN, TG left surgery 5/9/11. I have chronic bunion pain surgery at age 21. TG gave me back enough sitting to keep my job & join in some social activities. I wish the best to everyone! 2019 luck with orthotics from pedorthist & great PT allowing me to get off oxycodone.
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Violet M
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Re: PN or Levator Ani Syndrome

Post by Violet M »

I think it's really hard to distinguish between the two. I had PN but also had levator muscles that were painful, tight, and in spasm. The pudendal nerve runs through Alcock's canal which is the canal that runs between the obturator internus and the levator ani muscles. If the pudendal nerve is irritated, those muscles can be painful also.

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.
Simon94
Posts: 22
Joined: Thu Apr 13, 2017 9:01 am

Re: PN or Levator Ani Syndrome

Post by Simon94 »

The Pudendal nerve stuff is quite rare. I've been affected by pudendal injections and nerve tests etc.

I have not followed the TMS route 100%. With the pain for so bad, for so long, I'm having a hard time getting to truly believe that, A. Something that hurts this bad, can be subconsciously caused and B. That doing the mental work can actually make things which have been so tight, so bound up, and so irritated simply revers in my rectum.

But with that being said, nothing else has worked for this. I've seen the best physical therapists for pelvic pain, neurologists, you name it. All of course, have their own theories, but none of them seem to stick for a cure.

So, here I am again, and I think I have no other choice but to start doing the Sarno work full fledge. Maccafan has been a HUGE help and motivation as well!
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Violet M
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Joined: Mon Sep 06, 2010 6:04 am
Location: United States
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Re: PN or Levator Ani Syndrome

Post by Violet M »

Hi Simon,

What is maccafan?

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.
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