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Article Title:
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Taking the Shame out of Pudendal Neuralgia!

Article Description:
====================

Chronic pelvic pain has affected 15-30 percent of women and men 
in the world.  Finding a diagnosis and treatment can be quite 
challenging.  Some women and men with chronic pelvic pain have a 
very rare disorder called pudendal neuralgia.  Learn about the 
diagnosis, treatments and outcomes  from this extremely painful
neuralgia.


Additional Article Information:
===============================

1170 Words; formatted to 65 Characters per Line
Distribution Date and Time: 2006-10-26 10:12:00

Written By:     Violet Matthews
Copyright:      2006
Contact Email:  mailto:[EMAIL PROTECTED]



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Taking the Shame out of Pudendal Neuralgia!
Copyright (c) 2006 Violet Matthews
Society for Pudendal Neuralgia
http://www.spuninfo.org/



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.

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.

So, where exactly 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.

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 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.





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Ms. Violet Matthews has a Bachelor’s degree in nursing and has 
been an active member of a Pudendal Neuralgia forum for 2-1/2 
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://pudendal.info/phpBB2/ , and further information 
is available at http://www.spuninfo.org or  http://www.tipna.org/forum/index.php


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