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Based upon "Resonant Excitation Of Sexual Orgasms - Tao Of Love Coupling"
by Newman K. Lin, Ph.D., PE, a bridge between the Eastern Taoism Sexuality and the Western Engineering Science.==> [ORDERING THE BOOK]< =>[Why?]

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Case Study:  Chronic over-masturbation induced excessive epinephrine and inflammatory hormone prostaglandin E2 gave her clitoral pain/swelling and persistent sexual arousal symptoms after she got off birth control.
Reader: 2/12/2007>
Hello, So far the information on your website is very helpful. Altho, I think I've discovered my problem I would like some further insight and virtual diagnosis. I've been masturbating ( clitoral rubbing, no vibrator) since age 6. I've never had a problem with sexual orgasm although I noticed that it did take a long time for me to climax and I wore out my husband since I've been married (9 years now). I just turned 39,(African American) and for the last two years my orgasms have been mind blowing and extremely intense !( I like that part. Also, as a result, very very horny and I can't even look at a man without licking my lips. However, now I've discovered that I have PSAS and only masturbation and orgasm with or without husband can release clitoral pain/swelling. LOL! I think I may have burned out my neurotransmitters because I noticed now when I have orgasm, the euphoria is so intense that my eyes almost literally roll back in my head. I've been off the pill for two years now, almost exactly when my PSAS occurred. I occasionaly smoke marijuana (like once every three months or sometimes longer. Not a frequent user at all. I know it sounds scary! Please explain.
Dr. Lin: 2/13/2007> Your Persistent Sexual Arousal System is due to excessive inflammatory prostaglandin E2 release in your clitoral, vaginal and pelvic tissues, in conjunction with an excessive oxytocin, testosterone and/or DHT level in your bloodstream.  There are 3 types of clitoral and vulva swelling/inflammation:

Type I: Women or animal in heat:  When women and animals are heat, their clitoris, vulva and pelvic cavity are swollen without pains and extremely sensitized by Prostaglandin E1, E2 and E3, oxytocin, testosterone, DHT, Nitric Oxide, as described in http://www.actionlove.com/extra/animal.htm.  During the the in-heat state, the female always wants to be mated anytime. Once the female become pregnant, the fertilized-egg implantation and the placenta release progesterone and estrogen to trigger the pituitary to release prolactin and to stimulate the liver to release SHGB protein to freeze testosterone and DHT in the bloodstream. Therefore, the heat (Sexual Arousal) becomes subsided.  

Type II: Pregnancy:  The pregnant women's clitoris, vulva, uterus, cervix and pelvic cavity are swollen and enlarged without pains by Prostaglandin E1, E2 and E3, oxytocin, Nitric Oxide, and estrogen. If the placenta releases excessive estrogen and progesterone and the liver and pituitary continuously releases more and more SHGB and prolactin, respectively, in response to the continuous elevation of estrogen and progesterone,  the pregnancy will reduce or shut down sexual arousal or orgasm responses.  This means the swelling of the clitoris, vulva, uterus, cervix and pelvic cavity may not increase, but kill,  sexual arousal or orgasm ability. If the liver won't release sufficient SHGB protein so that the pituitary releases a high level of oxytocin with a low level of prolactin, pregnancy will boost sexual desire and orgasm responses, maybe leading to miscarriage.  Oral, implant or  injection birth controls use artificial progesterone and estrogen to mimics the pregnancy condition to shut down the hypothalamus-pituitary-ovarian axis, to overload (poison) the liver P450 detoxification system for excessive SHGB protein release and for reduction of neurotransmitters dopamine, acetylcholine and serotonin release,  to interfere with the thyroid function, and to reduce prostaglandins synthesis.  This is why the birth controls chemically castrate the female for no libido, sex and orgasm. When the liver fails to detoxify all the artificial progesterone and estrogen into natural ones, women on the birth controls can experience severe physiological and psychological disorders, vaginal discharge, clitoral and G-spot desensitization and erectile dysfunction, frigidity (lack of oxytocin and testosterone / DHT). Some unfortunately women get a permanent damage in the hypothalamus-pituitary and some experiences premature menopause after they get off birth control, as described in http://www.actionlove.com/extra/contracept.htm , http://www.actionlove.com/extra/shot.htm , and http://www.actionlove.com/extra/discharge.htm 

Type III:  Clitoral, Vulva, and Pelvic Inflammation:  Your persistent sexual arousal is an inflammatory responses to chronic release of epinephrine and prostaglandin E2  with excessive oxytocin, testosterone and DHT release while you got off birth control. Here, chronic over-masturbation keeps your epinephrine level high and constantly induce excessive inflammatory hormone prostaglandin E2, without prostaglandins E1/E3 and nitric oxide to repair the masturbation-damaged nerves, tissues and blood vessels; after you got off birth control, your liver and hypothalamus-pituitary-ovarian systems have been luckily and fortunately unlocked, your oxytocin, testosterone and DHT level in your bloodstream shot up too high and your prolactin and liver SHBG protein become too low to suppress your persistent sexual arousal and orgasm responses. Your inflammatory clitoris, vulva, G-spot, uterus, cervix, urethra and bladder will give you constant sexual arousal, pains, frequent urination urgency and orgasms. Please also read "The Root of Over-Masturbation/Excessive Sex: Male/Female Persistent Sexual Arousal Syndrome" - http://www.actionlove.com/extra/psas.htm  

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