Chronic over-masturbation results in non-bacterial (non-infected) prostatitis, urinary urgency, weak urine stream, interstitial cystitis (IC), bladder inflammation, pelvic pain, prostate pain, penile pain, low back pain, tailbone pain, rectal pain, inf

Case Study: Chronic over-masturbation results in non-bacterial (non-infected) prostatitis, urinary urgency, weak urine stream, interstitial cystitis (IC), bladder inflammation, pelvic pain, prostate pain, penile pain, low back pain, tailbone pain, rectal pain, inflammatory eye pressure, eye itchiness and redness, dark eye circles, eye oversensitity to light (pupil dilation), insomnia, ear buzzing, headaches, sadness, hair loss and graying

Reader: 3/21/2009>E-mail-1: Dr. Lin -
Thank you for your web site and research - it offers much better answers than I have received from traditional medicine.
I've already ordered your PinealTonin, ViaPal-N, and DopaFibra and started fish oil supplements based on your case studies but thought I'd better make sure I have the correct products.
I'm a 43 year old man. Over the last 25 years, I've used masturbation and sex to deal with stress. This has resulted in an average of masturbating 1x per day on average, but as much as 4x per day. I also tend to be a tightly wound, or stressful person anyway. I was diagnosed with prostatitis starting at age 28, and went on multiple rounds of antibiotics over the years since (no infection was ever found). I have been on Hytrin full time since 1998 to deal with near constant urinary urgency and weakness. About 3 years ago, I developed interstitial cystitis (inflamed bladder) and general pelvic pain, and then about 2 years ago, pain often during and after ejaculation (if too frequent) all along the penis but mainly at base and prostate, and near constant lower back pain emanating from around the tail bone. I've been on Neuront!n (Gabapentin) for the back pain for about 10 months. Ejaculatory fluid has dropped off markedly the last several years. Last year I had surgery for a rectal fissure that I've had for about 5 years that wouldn't heal. I have been on eyedrops (Travatan etc.) for very high eye pressure (low 30's untreated) for ten years 19990, and recently my eyes have become itchy and red often, with very dark skin along the nose and above the eye (somewhat less under the eye probably due to good skincare products). No floaters to speak of. I have noticed more memory problems the last couple years - and recently (past year) eye sensitivity to light in the am, and trouble fully waking up, and regular insomnia with extreme sensitivity to caffeine (and yes, I have always been sensitive to sounds, with some ear buzzing). Blood pressure (120/80) and blood sugar have so far been normal, but cholesterol and triglycerides have been high (LDL/HDL ratio ok though) last several years. Some headaches, unhappiness. My hair started thinning and graying in my 20's, and I started shaving my head last year as it was very receded, thin (on top)!
, and white.

I have never abused drugs and use no prescription drugs beyond what I've mentioned. I'm not married and tend to be a loner, with tendency toward negativity, although I have been actively working and very involved in community service. I also have trouble digesting alcohol (even small amounts will sit in my stomach for days). Last year I thought my problem was low body pH and have been on alkaline supplements (Alcabase/Tracelabs) and alkaline diet for about 8 months - which has for the most part resolved the interstitial cystitis and also long term athletes foot infection. I generally take regular vitamin/mineral supplements.

Thanks-

E-mail 2: Emailed earlier, wanted to add following. For the last few years I have had very low ambition, and just getting to work is a struggle. This is unusual for me. I have noticed that my ambition / ability to deal with things / plan, feel positive/happy, increases noticeably about 5-7 days after ejaculation (but I rarely get to this point). I always attributed this to guilt vs. real health.

Perhaps less important, I have a very strong affinity (compulsion) for carbohydrates, even binging on sugar at times. I had very bad acne from age 15-19. (very unusual in family).

How long can recovery take?

Thanks-

Dr. Lin: 3/22/2009>

Your problems are induced by chronic excessive norepinephrine/epinephrine and its inflammatory hormone prostaglandin E2 and histamine production from your scalp, brain/eyes/ears, pelvic area - the bladder, prostate, urethra, tailbone, perineum, joints, muscles, legs, hands and toes and fingers.
These sexual exhaustion symptoms and stress-induced inflammatory trauma disorders are given in
http://action.love/cases/case9848.htm
Excessive sexual activities triggers chronically excessive prolactin, norepinephrine/epinephrine, prostaglandin E2, cortisol and histamine release for chronic autoimmune disorders, pains, hair loss, sleeping disorder, headaches, skin disorders, visual disorders, ear ringing or buszing, joint infalmmatory pains, muscle cramps, bladder/prostate/urethral disorders and pains, and back pains
You will need ViaPal-hGH-P(3-010) and Pinealtonin (2-002, plus FishOil(1000 mg each meal) to help you gradually rejuvenate your neuro-endocrine function, power your dopamine/cholinergic/serotonin/GABA nervous function, reduce your stress hormone, prostaglandin E2 and histamine production, and boost your prostaglandin E-1/E-3 and Nitric Oxide production for healing.
http://action.love/mail/herbform.htm and you should take them for 4-6 months to reverse the neuroplasticity.

Postscript - The e-mails promoted Dr. Lin to write the following research conclusion:

Orgasm-stress induced inflammatory hormone prostaglandin E2 can over-excite mast cells to release histamine to activates the central histaminergic nerves and other numerous vasoactive, neurosensitizing and inflammatory molecules. Histamineand its receptors are very dense in the hypothalamus, heart, lungs and arteries; Psychological or physiological stress, including sex-induced stress, can induce significantalterations in both histamine synthesis and its concentrationin several brain regions. During stress reactions, histaminemay act as a neurotransmitter within the hypothalamus. A high densityof brain mast cells in regions situated at the boundary betweenthe central nervous system (CNS) and its surroundings suchas in the circumventricular organs and median eminence can induce immediate hypersensitivityeither in the CNS or in the periphery. This gives you orgasmic headaches, allergic responses, asthma, sneezing, sinus, itchiness, scalping burning sensation, hair loss and premature ejaculation. Histamine, in turn, may also trigger the release of various stress hormones to prolong your sex-induced stress for several days. Psychological or physiological stress, including orgasm/sex-induced stress also induces cardiac mast cell activation and histamine release into the bloodstream. Chronic excessive norepinephrine and its induced excessive histamine and prostaglandin E2 promote the development of atherosclerosis, coronary inflammation and cardiac ischemia, besides environmental toxins such as smoking (nicotine, pot, etc.). In myocardial ischemia, excessive norepinephrine release causes severe arrhythmias and sudden cardiac death. Recent studies shows histamine H3-receptors can provide a negative feedback control for the release of norepinephrine from the sympathetic nervous endings, and for a number of other neurotransmitters such as histamine itself, dopamine, GABA, acetylcholine, and serotonin. But, this negative feed control can be easily breakdown by excessive stress. On the other hands, histamine H1 and H2 receptors promote cardiac disorders. Reduction of endogenous histamine release or/and blockade of histamine H1 and H2 receptors can protects against ischemia. This is why there are a lot of reports about sudden death or cardiac arrest during intercourse or masturbation when histamine stimulates H1 and H2 receptors more than H3. And, severe allergy can cause cardiac arrest. However, what happens when histamine over-stimulates H3 but understimulate H1 and H2? In this regard, you will like to experience the sexual exhaustion symptoms resulted from post-sex deficiency of dopamine, acetylcholine, norepinephrine, serotonin and GABA. Unfortunately, in the most of sexual exhaustion symptoms we have collected, it seems H3 fails to negatively feedback control the norepinephrine and histamine release since sexual arousal, orgasm or ejaculation always triggers the hypothalamic and adrenal dopamine-norepinephrine conversion and histamine release when you are in the exhaustion state of the hypothalamus-pituitary-adrenal axis. For those with premature ejaculation, precum flooding, or premature orgasm, the sex organs start to release excessive histamine when norepinephrine and its induced prostaglandin E2 start to heat up the brain, sex organs and noradrenergic/adrenergic/sympathetic nervous systems. Our readers' urinary analyses always showed an excess of norepinephrine and a severe deficiency of serotonin. This indicates that under the stimulation of excessive inflammatory hormone prostaglandin E2 and prolactin in sexual exhaustion conditions, H3 fails to suppress the histamine and norepinephrine release, but it positively and successfully block the dopamine, acetylcholine, serotonin, and GABA release in the nervous terminals. You may wonder why sexual exhaustion symptoms are complicated by the exhaustion of the hypothalamus-pituitary-adrenal and -testicular axis as well as the destruction of the dopamine, cholinergic(acetylcholine)/vegal/parasympathetic, serotonin and GABA nervous functions, but with the excessive noradrenergic, adrenergic, sympathetic, histaminergic or/and glutamate nervous function.

In addition, excessive histamine stimulates excessive α-MSH release in the tissues around the eyes (dark eye circles), scrotum, labia majors or minors, perineum, inner thighs and even nipples, leading to skin darkness known as Hyperpigmentation. Thus, darkness of these skins indicate excessive histamine release locally. Beside excessive sex, other factors such as genetic factors, allergy, sleeping depletion (melatonin deficiency), sickness, and psychological stress, can also cause excessive α-MSH release. However, high-frequency sex will darken eye circles and labia minors very fast due to its induced poor local blood circulation and overall blood color change as result of excessive norepinephrine, epinephrine, prolactin and α-MSH in the bloodstream. For more information, please go to Excessive sex for darker eye cycles, nips, labia minors, pelvic area, perineum, clitoral and penile foreskin.

By the way, excessive norepinephrine and prostaglandin E2 in the brain causes Homosynaptic and Heterosynaptic plasticity, that is nervous damage or alternation. Homosynaptic plasticity alternates synaptic strength that results from the history of activity at a particular synapse. For examples, norepinephrine increases the noradrenergic and sympathetic nervous fires; epinephrine increases the adrenergic and sympathetic nervous fires. Serotonin Reuptaking Inhibitors outgrow the serotonin neurons and post-synapses and produces long-term inhibitory effects on the presynaptic terminals of the dopaminergic neurons. On the other hands, heterotropic plasticity changes synaptic strength that results for the activity of other neurons. For example, chronic norepinephrine stimulation under the noradrenergic/sympathetic nervous systems produces long-term inhibitory effects on the presynaptic terminals of neurons of the cholinergic/vegal/parasympathetic/serotonin/GABA neurons. This is why Drug and excessive Sex are so destructive to the brain, in particular, when alcohol opens the brain-blood barriers to allow more excitatory toxins and neurohormones (such as norepinephrine, epinephrine, glutamate, histamine and prostaglandin E2) to screw up the brain and nervous systems.

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