Taking The Shame Out Of Pudendal Neuralgia
Main Category: Women's Health / GynecologyAlso Included In: Urology / Nephrology; Neurology / Neuroscience
Article Date: 23 Oct 2006 - 11:00 PDT
'Taking The Shame Out Of Pudendal Neuralgia'
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What could possibly be worse than struggling with a painful condition and feeling ashamed to discuss the problem because of its intimate nature? Such is the case for many suffering with pudendal neuralgia, a little known disease that affects one of the most sensitive areas of the body. This area is innervated by the pudendal nerve, named after the Latin word for shame.
Due to the location of the discomfort combined with inadequate knowledge, some physicians make reference to the pain as psychological. But nothing could be further from the truth. Unfortunately, discussing the condition with gynecologists, urologists and neurologists often proves fruitless since most know nothing about the condition and therefore cannot diagnose it.
What is Pudendal Neuralgia?
Pudendal neuralgia is a chronic and painful condition that occurs in both men and women, although studies reveal that about two-thirds of those with the disease are women. The primary symptom is pain in the genitals or the anal-rectal area and the immense discomfort is usually worse when sitting. The pain tends to move around in the pelvic area and can occur on one or both sides of the body. Sufferers describe the pain as burning, knife-like or aching, stabbing, pinching, twisting and even numbness.
These symptoms are usually accompanied by urinary problems, bowel problems and sexual dysfunction. Because the pudendal nerve is responsible for sexual pleasure and is one of the primary nerves related to orgasm, sexual activity is extremely painful, if not impossible for many pudendalites. When this nerve becomes damaged, irritated, or entrapped, and pudendal neuralgia sets in, life loses most of its pleasure.
Where is the pudendal nerve?
It lies deep in the pelvis and follows a path that comes from the sacral area and later separates into three branches, one going to the anal-rectal area, one to the perineum, and one to the penis or clitoris. Since there are slight anatomic variations with each person, a patient's symptoms can depend on which of the branches are affected, although often all three branches are involved. The fact that the pudendal nerve carries sensory, motor, and autonomic signals adds to the variety of symptoms that can be exhibited.
Diagnosis
Because pudendal neuralgia is uncommon and can be similar to other diseases, it is often misdiagnosed, leading some to have inappropriate and unnecessary surgery. Early in the diagnosis process, it is crucially important to undergo an MRI of the lumbar-sacral and pelvic regions to determine that no tumors or cysts are pressing on the nerve. In addition, the patient should be screened for possible infections or immune diseases, as well as having an evaluation by a pelvic floor physical therapist to determine the health of the pelvic floor muscles and to uncover whether skeletal alignment abnormalities exist. An accurate patient history is needed to assess whether there has been a trauma or an injury to the nerve from surgery, childbirth, or exercise. Tests that offer additional diagnostic clues include sensory testing, the pudendal nerve motor latency test, and electromyography. A nerve block that provides several hours of relief is another tool that helps to determine if the pudendal nerve is the source of pain.
One of the most common symptoms that accompanies pudendal neuralgia is severe depression. Some people with the disease have committed suicide due to the intractable pain. For that reason, it is important to consider antidepressants, as they can help lessen the hypersensitivity of the genital area in addition to relieving bladder problems. Certain anti-seizure drugs reportedly help to alleviate neuropathic pain while anti-anxiety drugs provide substantial relief of muscle spasms and assist with sleeping.
Uninformed physicians are reluctant to prescribe opiates for an illness that shows no visible abnormality, yet the desperate nature of genital nerve pain requires that opiates be prescribed for these patients. While medications are not always satisfactory, they do help take the edge off of the pain for many people. Until the correct treatment is determined, it is imperative that patients with pudendal neuralgia receive adequate pain management since the pain associated with this illness can be intense.
Treatment
Treatment depends on the cause of distress to the nerve. When the cause is not obvious patients are advised to try the least invasive and least risky therapies initially.
-- Physical therapy that includes myofascial release and trigger point therapy internally through the vagina or rectum assists with relaxing of the pelvic floor, especially if pelvic floor dysfunction is the cause of nerve irritation. If no improvement is found after six to twelve sessions, nerve damage or nerve entrapment might be considered.
-- Botox is now used in medical settings to relax muscles and shows promise when injected into pelvic floor muscles; though finding a physician adept at this treatment is difficult.
-- Pudendal nerve blocks using a long-acting analgesic and a steroid can reduce the nerve inflammation and are usually given in a series of three injections four to six weeks apart.
-- If physical therapy, Botox, and nerve injections fail to provide adequate relief, some patients opt for pudendal nerve decompression surgery.
There are three published approaches to pudendal nerve decompression surgery but there is debate among members of the pudendal nerve entrapment community as to which approach is the best. Since there are advantages and disadvantages to each approach, patients face considerable confusion when deciding which type of surgery to choose. Because there are only a handful of surgeons in the world who perform these surgeries, most patients have to travel long distances for help. Moreover, the recovery period is often painful and takes anywhere from six months to several years since nerves heal very slowly. Unfortunately, early statistics indicate that only 60 to 80 percent of surgeries are successful in offering at least a 50 percent improvement. Patients whose surgeries are not successful or who do not wish to pursue surgery have the option of trying an intrathecal pain pump which delivers pain medication locally and helps to avoid some of the side effects of oral medications. Others pursue the option of a neurostimulator either to the sacral area or directly to the pudendal nerves. These are relatively new therapies for pudendal neuralgia so it is difficult to predict success rates. Some pudendalites have devised ingenious contraptions for pain relief ranging from u-shaped cushions cut from garden pads all the way to balloons filled with water, frozen, and inserted into the vagina. Most have a favorite cushion for sitting and many have special computer set-ups for home and office use in order to avoid sitting. Generally speaking, jeans are a no-no, so patients revise their wardrobes to include baggy pants and baggy underwear - if they are able to tolerate wearing underwear.
Clearly more research is required to find effective methods to better manage the pain and debilitation of pudendal neuralgia. But in the meantime, friends and family close to those who have this devastating illness play a huge role in helping patients cope, thereby maintaining the best quality of life possible. Support, love and understanding are of primary importance for those suffering with this affliction.
Written by: Ms. Violet Matthews
Please also view the article "Taking The Myths Out Of Pudendal Nerve Entrapment Surgery"
Ms. Violet Matthews has a Bachelor's degree in nursing and has been an active member of a Pudendal Neuralgia forum for 2 years. Having suffered with Pudendal Neuralgia, she has seen a 75% improvement in quality of life since her pudendal nerve decompression surgery in France two years ago. Married with two children, Ms. Matthews resides in Southwestern United States. You can usually find Violet at http://pudendalhope.org/forum/.
Further information is available at http://www.spuninfo.org or http://www.tipna.org/forum/index.php.
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Visitor Opinions (latest shown first)
Total 90 opinions, latest 20 shown. For all opinions, click through to the full thread.Is There Life After Pudendal Surgery?
posted by Crystal on 6 May 2012 at 9:27 pmI have been dealing with Chronic pain for 6 years, after recently having vaginal mesh removed, I have now been diagnosed with pudendal issues. I have had all tests and then some. I am going to have the surgery, but I need to know how long I will be out of work. Any ideas?? I'm already being accused of having an attendance problem, bc I've have 7 surgeries in 6 years.
Someone Help Please.
posted by Jennifer from canada on 9 Apr 2012 at 6:24 pmhi my name is jenn i live in canada i suffer from PNE do to a trama to my pelvis but never had an issue until a surgery to fix my pelvis .i am a single mom of an 8yr old girl who cries nightly wanting her happy mom back.right now i feel as if life is pointless as im stuck in bed un able to barely walk from the severe severe pain that i deal with daily i have been searching for almost a year to find a doctor that can preform surgery to correct the PNE please someone anyone this is my cry for help and to get my life back i am willing to travel to where i may have to in order to have the surgery done.can anybody help please my daughter needs her mommy and i need to love life again and myself.thanks.
PT Tips
posted by hopeful! on 13 Mar 2012 at 7:42 pmTrying this again. Stephen Frost mentioned physical therapy as being helpful. Exactly what are you doing. thank you kindly.
Ottawa Dr. for Pudental neuralgia
posted by diame on 28 Jan 2012 at 4:25 pmPlease? does anyone know an Ottawa PN dr yet?
Follow-up Question
posted by Jim on 18 Nov 2011 at 4:00 pmI respect that you have solved your PNE condition through exercises. Can you elaborate for the rest of us just what you did to get better?
Pudential neuralgia
posted by Cathy on 7 Nov 2011 at 7:19 pmI have gone through all the treatments, meds. injections etc. for pain in my butt and legs, it gets worse all the time. I live in MN and my Doc is suggesting strongly surg. now and I know that I can't go on like this but would like info on results of surg. HELP
PNE Surgery
posted by KT on 7 Nov 2011 at 5:42 amI had PNE surgery recently. Am open to corresponding about it by email to anyone looking for more info. itsjunk2u (at) gmail.com
-KT
Pudendal Hydro-disecton Neuroplasty
posted by krista on 6 Nov 2011 at 11:00 amHi, I have PNE and underwent 2 pudendal hydro-disection neuroplasty procedures in Philadelphia and I am confused as to if my resulting pain is due to inflammation or if thier is still nerve entrapment present... I am interested in surgery if it will end my pain. Any thoughts or opinions would be greatly appreciated. Krista
Pudendal Surgery
posted by Linda on 15 Sep 2011 at 6:43 pmYour site was posted in 2007, but you sound like me crying out for help. Everyone thinks I am crazy, I spend my days in pain. Did you ever find any help, I pray you did, I have been living this for about 5 yrs now. I am afraid my pain will outlive me..
Linda
Is there any hope?
posted by Laurie on 12 Sep 2011 at 1:31 pmI had bilateral tg approach surgery may 2011 and so far (Sept '11) have had no improvement in pain. The day after surgery I experienced left buttock and leg sciatica - which gets worse w weight-bearing and walking. The pudendal pain is worse but now I can't walk much and need a wc - that is if I go anywhere.
So it's been 4+ months postoperative. Is there any hope that this will get better if no improvement yet?
I take vicodin, 20mg w 10mg Ativan for pain but need none at night. As many have posted...this does just about ruin your life. I am desperate to get rid of this disabling pain.
Dennra from SF bay area.
This Is High Risk Surgery With Unpredictable Outcomes
posted by Emile on 9 Aug 2011 at 12:12 pmI am 62 and was diagnosed with chronic non-bacterial prostatitis when I was 40. After seeing several urologists over a number of years it was clear they had no idea how to treat my condition nor did have any idea what caused the symptoms and annoyingly they also find the condition uninteresting. Prostatitis merely means inflamed prostate, it is a diagnosis without meaning. The new name many doctors are using is chronic pelvic pain syndrome or CPPS. Clearly this is an equally useless name that tells us the medical community has no understanding of the underlying pathology.
My initial symptoms were frequent urination, weak urine stream, weak ejaculations and occaisional pain at orgasm.
About five years ago my symptoms progressed and I developed numbness in the rectal area, a feeling of a foreign body in the rectum and erectile disfunction.
Eventually my research led me to conclude I had pudendal nerve neurology and I consulted one of the few doctors in the United States that specialize in pudendal nerve entrapment and he confirmed the diagnosis and commenced treatment.
I have a graduate degree in biology and have published peer reviewed papers. I know physiology and anatomy and understand my disease as well or better than the run of the mill urologists I have seen.
After consulting with one of the "experts" on pudendal nerve pathology I underwent a series of three pudendal nerve blocks containing the powerful steroid prednisone and a local anesthetic similar to novacaine. I considered the treatment results to be valueless.
So what do I do? I NEVER sit in a normal way. I have not sat down for three and one-half years. I either stand or kneel. When I drive my car I have configured a device that allows me to lean forward and essentially sit on my thighs. I drive a van since this works best and I am able to drive for six or seven hours although the pressure on my thighs does become uncomfortable. I also cannot lean forward and pick things up without increasing the numbness I feel in my rectum, so I bend my knnes until I am resting on one knee before I try to pick anything up.
I am lucky because I feel numbness rather than the severe pain many of you must endure. My doctor said this usually indicates more nerve damage.
At any rate I have reviewed the scientific literature in depth as well as the anatomy of the pelvic area. There are a lot of organs, ligaments, nerves, muscle etc. packed into this area and most of the surgical methods for PNE cut through the tissue in a method I would describe as barbaric. The damage done by these surgeries is great and most of the medical literature offers very little reason to be optomistic of a good outcome.
Recently I did read papers by Aaron Filler, a surgeon in Santa Monica who uses a different approach. He uses MRI guided surgery that is much less invasive than the other surgical methods available. Note however that he does not accept insurance so expect to pay some hefty fees if you choose to see him. I do not know how successful his techniques are but his methodology surpasses all others I have investigated. For now I will continue to wait until research confirms tecniques with a high liklihood of success.
Surgery
posted by Greg Geisler on 9 Jul 2011 at 2:39 pmI had the pudendal nerve decompression surgery in sept 2010, so I am 9 months post-op. Still have sugnificant pain, some days worse than others. I started PT and I can sense some incremental improvement. Would be nice to hear from others who have had the surgery to see how long their recovery took, and treatments they did, if any, to help with recovery.
Any Good Results?
posted by Terry on 5 Jul 2011 at 1:57 pmMy husband has been suffering for several years with severe rectal pain. He has been through many tests and procedures. Every alternative and conventional medical treatment that we thought could possibly help. Botox injections,accupunture, many therapies, surgery to relieve muscle tension, he also had a neuro stimulator implanted in November which is not helping. He is on oxycodone and lyrica (not helping) The pain started out occurring a few times a day, this past year it has gotten to where he has a spasm every half hour and now it is almost constant. I'm thinking that maybe it could be PNE, but not really sure. Has anyone else had this type of pain and found a cure? We would appreciate any help. God Bless you.
Pudendal neuralgia
posted by Miljenko on 8 May 2011 at 9:09 amHy
I have PN. I am taking Amytriptilin and some abticonvulsive and B vitamins. But id doesn't help. Can anybody tell me the solution?
Dr. Hibner In Phoenix
posted by Norm on 11 Apr 2011 at 9:37 amPlease consider Dr. Michael Hibner in Phoenix, AR. He is a gynocologist, treating both women and men with PNE. He has the technology and team to image the pudendal nerve with all three branches, and interpret specifically where the entrapment lies, or whether there is an entrapment at all. This should establish your data and baseline for further treatment. Highly recommended.
PNE Nearly Gone
posted by Stephen Frost on 7 Feb 2011 at 9:35 pmHi All
I was suffering really badly with PNE and the doctors
couldn't help me. The only thing they suggested was
surgery or painkillers which I was really against, so
I took matters into my own hands.
I started a routine of exercises that I could do at home
which were really simple and over the past six months,
the discomfort has almost completely gone. I only feel
a slight twinge now and then, which compared to what
it was, is like a miracle.
I'm hoping just a few more months will completely rid
me of the curse of PNE.
I have trained in fitness and personal training, so I do know
what I'm doing.
Keep well.
Steve
Pne Doctors In Houston
posted by Anon on 6 Feb 2011 at 7:12 pmI am thinking about having PNE surgery at Houston.I would to talk to some who has had the surgery in Houston. What do think about the doctors who did your surgery?
Three Entrapments
posted by Jane on 4 Feb 2011 at 7:21 amHi Theresa, I have read your story and would like to know some more facts if you would share with me. I had bilateral entrapment following surgery. Had nerve blocks to no avail. Then had the right PN decompressed which is still pretty good today, then the left one about 2 years after the right. It was going well and then the pain returned. I'm not sure where to go now (the Dr has retired) and wonder if like you the nerve is entraped in another place. How did your dr find out you had three entrapments? Would you be kind enough to e-mail me;
j.kitteridge (at) btinternet.com Many thanks.
London Based Doctors
posted by Jane on 4 Feb 2011 at 7:10 amHi Jane, I am also a Jane based just outside of London. I have been battling with PN bilateral entrapment following an operation for 5 years. Had four nerve blocks that did'nt work and eventually both nerves have been decompressed. I do have some contacts for you. Feel free to e-mail me; j.kitteridge (at) btinternet.com
PN Surgery
posted by Jane on 4 Feb 2011 at 7:05 amHi Jenny, following sugery I had bilateral PN entrapment. I also had four nerve blocks, anaesthetic injected directly but all to no avail. I eventually had both sides decompressed surgically at different times. The right first is pretty good - two years later the left, which was good but deteriorated, why I don't know. Feel free to e-mail me for more information on this;
j.kitteridge (at) btinternet.com
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