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PN Links
The following links may be helpful in diagnosing or treating
your condition. If you would like to suggest a new link, please
post a message in the Community forum.
General Information
PN Insurance Information
- Les has prepared a collection of documents that he has found
extremely useful for convincing an insurance company to pay
up. They also contain info on treatment outcome success and
other subjects. Please send him an email requesting this information
and he will reply with attachments. Thanks Les!
Sitting
Cushion - The overall best special sitting cushion for
PN seems to be these. Note the cutout in the center, where
the area served by the pudendal nerve is located. The 3"
thick model is the favorite. And the price is right, at only
$23.00. Like all foam cushions, if you have to you can carve
it a little further for a custom fit. Thanks Celeste!
Other PN Websites
Groupement
Européen de Périnéologie - A very
interesting European site which calls PNE "pudendal canal
syndrome." Much of this site is in French, who apparently
are the world's experts in perineum conditions. The site is
under construction. Also see the home
page.
Pudendal.Info - This
is the forerunner of tipna.org. They too have a forum.
PudendalNerve.Info
- This is Pudendal Nerve Resources. They too have a forum.
Conditions Related to PN
Coccydynia - Coccydynia
is pain in the tailbone, aka the coccyx. As the site says,
"Coccyx pain is often caused by falling backwards or
by childbirth, though the cause of pain is unknown in about
a third of cases. It makes it very painful to sit down. There
are effective treatments available, and the great majority
of sufferers can be cured."
Neuropathy
HealthBoards - This is a disscussion group for neuropathy
in general.
Persistant
Sexual Arousal Syndrome - This is a rare but real condition
affecting women. This is a link to the Yahoo group, described
as: "Discussion and Support for Women with Persistent
Genital Arousal, better known as PSAS."
Prostatitis - The
Prostatitis Foundation.
Vulvodynia - There are
many sites on this. This link is the National Vulvodynia Association.
Do a search on "vulvodynia" for many more.
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