PEA

Published Reports and Medical Information
Useful links to PN related articles.
Griff522
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PEA

Post by Griff522 »

I'm a newbie when it comes to research but I stumbled across this and thought I would share ;)

http://onlinelibrary.wiley.com/doi/10.1 ... x/abstract
Burning vulva pain began 10/09
Treated for SIJD 9/10 and burning stopped and pain localized to rt side
Surgery w/ Dr Dellon 5/11 - didn't help my pain
2012 - PT, massage therapy, and ART therapy from chiropractor
MRI showed labral tear and US of groin found hernias
2/13 - surgery for sports hernia
5/13 - still have obturator internus spasms
5/13 - appt with ortho spine dr
8/16/13 - Arthroscopic surgery to rt hip for FAI and torn labrum
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Karyn
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Joined: Fri Sep 17, 2010 12:59 pm
Location: Lowell, MA

Re: PEA

Post by Karyn »

Sounds interesting! Is anyone able to view the full article? I'm still not sure what it is or how it works.
Thanks, Griff!
Warm regards,
Karyn
Ultra Sound in 03/08 showed severely retroverted, detaching uterus with mulitple fibroids and ovarian cysts.
Pressure and pain in lower abdomen and groin area was unspeakable and devastating.
Total lap hysterectomy in 06/08, but damage was already done.
EMG testing in NH in 04/10 - bilateral PN and Ilioinguals
3T MRI at HSS, NY in 09/10
Bilateral TG surgery with Dr. Conway on 03/29/11. Bilat ilioinguinal & iliohypogastric neurectomy 03/12. TCD surgery 04/14.
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Violet M
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Re: PEA

Post by Violet M »

I can see how this might be helpful in case of an inflammation but I think there are certain types of entrapments that could not be helped just by taking an anti-inflammatory drug. Here is a copy of the abstract in case the link eventually quits working.

Abstract

Background.  Pudendal neuralgia is a cause of chronic, disabling, and often intractable perineal pain presenting as burning, tearing, sharp shooting, foreign body sensation, and it is often associated with multiple, perplexing functional symptoms.

Case Report.  We report a case of a 40-year-old man presenting with chronic pelvic pain due to pudendal nerve entrapment and successfully treated with palmitoylethanolamide (PEA).

Conclusion.  PEA may induce relief of neuropathic pain through an action upon receptors located on the nociceptive pathway as well as a more direct action on mast cells via an ALIA (autocoid local injury antagonism) mechanism.

As recently demonstrated in animal models, the present case suggests that PEA could be a valuable pharmacological alternative to the most common drugs (anti-epileptics and antidepressants) used in the treatment of neuropathic pain.
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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Cora
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Re: PEA

Post by Cora »

Interesting, as this is getting some attention on another pelvic pain site. My understanding is that it is only available in Europe. If people are interested, I could try to get more info.
And to confuse you a little more, I have a new user name...once again.. But have the same old avatar, same old me, same old signature.
Anyway... as for PEA, it's garnering some attention here, just not sure about local availability.

Cora
Onset PN/PFD/centralized pain in Oct 06 after years of athletics,nursing career and dog training. PT for two years with improvement, now go for tune-ups and pain management. Stopped Cymbalta, was on M.S. Contin, then Kadian, and briefly Methadone for pain management, now off those meds and pain is well managed with Buprenorphine. Followed my pain management specialist.
PN-SufferVT
Posts: 87
Joined: Fri Oct 22, 2010 8:46 pm

Re: PEA

Post by PN-SufferVT »

My wife is a doc, I will have her get the full article from the hospital computer. I'll keep everyone posted.
PN started in June 2009, quickly pain level went to 10. PN probably caused from long hours sitting in car, followed by weightlifting/sports daily. My pain level are now daily between 1 and 4. I do not know if I have true entrapment, but definitely know I have neuralgia of the PN.
PN-SufferVT
Posts: 87
Joined: Fri Oct 22, 2010 8:46 pm

Re: PEA

Post by PN-SufferVT »

I found some great research on this. However, it is in Italian, so you will need to open it in Google Chrome Browser to translate. It is called Normast overseas and it looks like they are have a lot of success treating pelvic pain with it.....

In pudendal neuropathic pain palmitoylethanolamid reduced the pain scores in a clinical relevant way. [8] In another paper the positive effects on pelvic pain were reported. [9] Animal studies are also supportive for the use of this supplement in the treatment of neuropathic pain. [10]

[8]: Calabrò RS, Gervasi G, Marino S, Mondo PN, Bramanti P. | Misdiagnosed chronic pelvic pain: pudendal neuralgia responding to a novel use of palmitoylethanolamide. | Pain Med. | 2010 May;11(5):781-4. Epub 2010 Mar 22.
[9]: Indraccolo U, Barbieri F. | Effect of palmitoylethanolamide-polydatin combination on chronic pelvic pain associated with endometriosis: preliminary observations. | Eur J Obstet Gynecol Reprod Biol. | 2010 May;150(1):76-9. Epub 2010 Feb 21.

http://www.epitechgroup.it/scripts/sys/ ... gina_id=28
PN started in June 2009, quickly pain level went to 10. PN probably caused from long hours sitting in car, followed by weightlifting/sports daily. My pain level are now daily between 1 and 4. I do not know if I have true entrapment, but definitely know I have neuralgia of the PN.
PN-SufferVT
Posts: 87
Joined: Fri Oct 22, 2010 8:46 pm

Re: PEA

Post by PN-SufferVT »

Cora wrote:Interesting, as this is getting some attention on another pelvic pain site. My understanding is that it is only available in Europe. If people are interested, I could try to get more info.
And to confuse you a little more, I have a new user name...once again.. But have the same old avatar, same old me, same old signature.
Anyway... as for PEA, it's garnering some attention here, just not sure about local availability.

Cora
What other site is it getting attention on?
PN started in June 2009, quickly pain level went to 10. PN probably caused from long hours sitting in car, followed by weightlifting/sports daily. My pain level are now daily between 1 and 4. I do not know if I have true entrapment, but definitely know I have neuralgia of the PN.
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Cora
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Re: PEA

Post by Cora »

sorry for the delayed response, the site that a lot of people are using this on is the yahoo site, Happy Pelvis

Cora
Onset PN/PFD/centralized pain in Oct 06 after years of athletics,nursing career and dog training. PT for two years with improvement, now go for tune-ups and pain management. Stopped Cymbalta, was on M.S. Contin, then Kadian, and briefly Methadone for pain management, now off those meds and pain is well managed with Buprenorphine. Followed my pain management specialist.
PN-SufferVT
Posts: 87
Joined: Fri Oct 22, 2010 8:46 pm

Re: PEA

Post by PN-SufferVT »

Hey Everyone,
Here is a new study on PEA for CTS of the wrist..... I have also found a website where you may purchase PEA..... it is really promising!

Use of palmitoylethanolamide in the entrapment neuropathy of the median in the wrist.
Conigliaro R, Drago V, Foster PS, Schievano C, Di Marzo V.
Source
Operative Unity of Neurology, Siracusa, Italy - robconi@tin.it.
Abstract
AIM:
Carpal tunnel syndrome (CTS) is a medical condition in which the median nerve is compressed, leading to discomfort and pain. Palmitoylethanolamide (PEA) is an endogenous fatty acid amide, able to modulate inflammatory cell reactivity and pain. This study deals with the capability of PEA to normalize the electroneurographic alterations associated with moderate CTS.

METHODS:
Patients displaying moderate CTS were enrolled and daily PEA (600 mg or 1 200 mg/die) was administered for 30 days. Control group received no treatment.

RESULTS:
PEA treatment significantly improved the CTS-induced reduction of median nerve latency time (P<0.0004); PEA effect was dose-dependent. Tinel's sign presence and symptoms of discomfort were also reduced.

CONCLUSION:
Although further studies are needed to better characterize PEA effect, the present report represents the first evidence on the improvement of distal motor latency elicited by PEA in patients with moderate CTS. The data support the hypothesis of protection against inflammatory and neuropathic pain by PEA.
PN started in June 2009, quickly pain level went to 10. PN probably caused from long hours sitting in car, followed by weightlifting/sports daily. My pain level are now daily between 1 and 4. I do not know if I have true entrapment, but definitely know I have neuralgia of the PN.
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Bladder Facts
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Re: PEA

Post by Bladder Facts »

Hello, :D

Yesterday I started a new topic, see http://www.pudendalhope.info/forum/view ... =25&t=2243

Maybe we could start again talking about the compound Palmitoylethanolamide.

I have lots of new articles....
www.ic-today.com
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