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Welcome to the Orgasm & BrainWash Engineering Center where "BrainWash" is defined as an alternation of gene and enzyme expression in your 3 brains - the head, gut and pelvic cavity. 

Orgasm Research Center established in 1997, starting from LinPlaza.com.
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Welcome to Orgasm Research Center
Suffering is Believing
(This is what you don't want to know!)
or get Benefits from Optimal Orgasms (This is what you love to hear about) or More!

This link will give you the following topics:
1. Destruction of Excessive Orgasms
2. Ejaculatory Frequency and Seasonal Change vs Semen Quality
3. Ejaculation Frequency vs. Testosterone Level
4. Sex as a Drug 
5. Excessive sex for darker eye circles, nips, labia minors, pelvic area, perineum, clitoral and penile foreskin
6. Benefits from Optimal Orgasms
7. Brain-Skin/Brain-Hair connection - the effect of excessive sex-induced stress on skin (acne) and hair (hair loss)
8. Orgasm Brain Sex Pain examples

Destruction of Excessive Orgasms
After you enjoyed too many sexual orgasms and/or too much pleasure, you have likely blown your brain/nervous bioelectric circuit breaker, and may have started to deal with the Sexual Exhaustion Symptoms - the exhaustion of the hypothalamus-pituitary-adrenal/-testicular axis,  very possibly or likely including the hypothalamus-pituitary-thyroid dysfunction too, resulting from the Nervous Excitotoxicity and Inflammation induced by excessive norepinephrine, epinephrine and glutamate (& other excitory neurohormones, for a short-term pleasure reward and the long-term dopamine depletion)  and Prostaglandin E2!  The Traditional Chinese Medicine has termed the hypothalamus-pituitary-adrenal (HPA) exhaustion as "Kidney Deficiency", since the classic Chinese anatomy text assumed the tiny adrenal gland, sitting on the top of  the kidney, is a part of the kidney about 2000 years ago. The HPA exhaustion results in the erratic release of CRH (corticotropin releasing hormone), POMC (proopinomelanocortin),  ACTH (adrenocorticotropc hormone),  ß-lipotropic hormone, ß-endorphin, α-melanocyte-stimulating hormone (α-MSH),  ß-MSH, CA (catecholamines) and TSH (thyroid stimulation hormone), in response to stress, sex and environmental/dyshomeostatic stimuli.  Since skin and hair follicles also display a functional equivalent of the HPA axis, sexual exhaustion will also extensively affect your skin (for examples: darkening skins in certain areas such as eye cycles, nips, labia minors, foreskin, perineum and groins, due to excessive release or trapping of the POMC peptide α-MSH which is also an anti-inflammatory and immunomodulating hormone - anti-tissue abrasion!) and the hair (for examples: hair loss in the scalp and gray hair, but it won't grow hair in your palms although it will destroy your HPA axis.)  The explanation of the HPA, skin and hair connection are given in the following links: http://edrv.endojournals.org/cgi/reprint/21/5/457, http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=1839836&blobtype=pdf , http://www.fasebj.org/cgi/reprint/04-1968fjev1.pdf,  http://www.tufts.edu/sackler/pharmacology/faculty/theoharides/documents/TiI-brain-skin.pdf , http://physrev.physiology.org/cgi/reprint/80/3/979 , http://ard.bmj.com/cgi/content/abstract/66/suppl_3/iii52 , http://www.ncbi.nlm.nih.gov/pubmed/12576179 , http://www.fasebj.org/cgi/reprint/19/10/1332.pdf, http://www.annalsnyas.org/cgi/content/abstract/885/1/350 , and http://www.jci.org/articles/view/33508/pdf
As a result, sex is like a good investment with a bad return. When you reach the neuro-endocrine breaking point, it is like the stoke market cash leading to the great depression!! Yes,  excessive sex induces psychological and physiological disorders.

For example: After sexually exhausting his the brain's and internal Hypothalamus-Pituitary-Adrenal (HPA) axis, he has gotten headache and felt death and exhaustion from wet dream, even once a weak. Why he felt worse on the 2nd day after ejaculation? He may have to rely on  the Cutaneous Hypothalamus-Pituitary-Adrenal (CHPA) function to assist post-ejaculation or post-orgasm recovery.
http://www.actionlove.com/cases/case15761.htm

After our 10-year case collection and research, we now understand why excessive sex and drug abuses are so destructive. We are able to zoom into the main causes:
1.  Sex-induced excessive excitory neurohormones norepinephrine/epinephrine/glutamate/histamine production for nervous toxicity: According to a American Scientists's report - http://www.americanscientist.org/template/AssetDetailNoFrame;jsessionid=aaaaBjcbX4%0D%0AuGmh?assetId=49707),   epinephrine can easily penetrate the mouse's blood-brain barrier into the limbic system, and allow lupus-like autoantibodies to reach the amygdala, where " the antibodies bind to and overactivate certain cell receptors, eventually killing the cells through excitotoxicity."  Excessive dopamine-norepinephrine-epinephrine conversion during sexual arousal/orgasm/ejaculation will drop the dopamine level (yes, for dopamine excitotoxicity prevention and rewarding pleasure if your dopamine level is too high!) , leading to excessive pituitary prolactin release to cause testicular and ovarian disorders, and keep the stress neurohormone norepinephrine or/and epinephrine in the excitotoxicity level. Our readers also reported chronic excessive orgasm/ejaculation induced seizure, headache, migraine, blackout, allergy, asthma, eye floaters and ear ringing (tinnitus), as a result of nervous excitotoxicity induced by excessive norepinephrine, epinephrine (particularly this one), glutamate or/and histamine. Prolonged and repeated assaults on the hippocampus nerve cell structure may permanently fry your brain. (Here are the other recent research examples:
http://jcem.endojournals.org/cgi/reprint/87/9/4245
http://www.biomedcentral.com/1471-2172/5/22
http://circ.ahajournals.org/cgi/content/full/102/1/96
http://www.algonot.com/pdf/mastcellsinflammation.pdf
http://www.ionchannels.org/showabstract.php?pmid=15970488
http://www.pnas.org/cgi/reprint/103/3/678
http://www.sciencemag.org/cgi/content/abstract/174/4008/512,
http://www.pnas.org/cgi/content/full/96/12/7093
http://ajpheart.physiology.org/cgi/content/full/289/4/H1577 
http://jcem.endojournals.org/cgi/content/full/89/5/2000
http://www.anesthesia-analgesia.org/cgi/content/full/100/2/520
http://www.osti.gov/energycitations/product.biblio.jsp?osti_id=6793231, as addressed in this link-

How to kick the pornography addiction:  Reduction of the inflammatory hormone prostaglandin E2 production, Excessive epinephrine and norepinephrine induces inflammatory responses, persistent sexual arousal, and brain/nervous excitotocixity, and enhancement of the serotonin and GABA nervous modulation and control
==> http://www.actionlove.com/cases/case15570.htm
). 

Dopamine and glutamate are essential for sex. For healthy person, sexual stimulation elevates the dopamine and glutamate synthesis. Excessive dopamine triggers the stress hormone production and promotes the liver P450 enzymes and Monoamine oxidases (MAO) to  deamination of dopamine and stress hormones. In addition to elevating the stress hormones norepinephrine and epinephrine,  chronic excessive sexual stimulation, excessive orgasm, over-masturbation/over ejaculation, or drug abuse will result in excessive glutamate release or accumulation due to a shortage of the enzyme L-glutamic acid decarboxylase and pyridoxal phosphate in efficiently converting elevating glutamate into GABA during sex, or/and due to a shortage of the enzymes gamma-glutamylcysteine synthetase and glutathione synthetase or/and a shortage of  amino acids L-cysteine and glycine, in converting elevating glutamate into the liver detoxification promoter Glutathione.   Elevation of GABA with serotonin, norepinephrine and prolactin after sex or orgasm will trigger the pineal gland to release melatonin for sleeping and restoration;  Elevating of glutathione can reduce the formation of  oxidative toxins, such as Hydrogen peroxide (H2O2),  associated with oxidative injury and cellular/nervous damage. Of course, you will benefit from sex and orgasm if you get a resulted elevation of both GABA and glutathione.  However,  when the liver are stressed out by orgasm, over-ejaculation, drugs, and aged/toxified by the monoamine oxidization toxins, the liver can not efficiently provide the enzyme L-glutamic acid decarboxylase and pyridoxal phosphate for glutamate-GABA conversion, leading to accumulation of glutamate in the brain/nervous systems and cerebrospinal fluid for ultimate nervous and brain destruction. ( Note that increasing the conversion of L-arginine to the inhibitory neurotransmitter agmatine can help block the action of glutamate on the NMDA receptor and acts as a neuromodulator. This is an important mechanism in preventing the harmful effects of excess glutamate. Agmatine is decarboxylated argenine. Studies shows agmatine can reverse pain induced by inflammation, neuropathy, and spinal cord injury - http://www.pnas.org/cgi/content/abstract/97/19/10584 ).

Furthermore, chronically excessive sexual arousal, over-ejaculation (overmaturbation), excessive orgasms or/and drug abuse can hyperativate the enzyme Monoamine oxidases (MAO) for dopamine-DOPAL conversion , where DOPAL stands for 3,4-dihydroxyphenylacetaldehyde.  DOPAL is a potent neurotoxin to cause Parkinson's-like brain lesions, and its resulted cognitive impairment is very similar to autism. In addition to DOPAL, norepinephine and epinephrine can be converted to 3,4-dihydroxyphenylglycoaldehyde (DOPEGAL) by MAO too. DOPEGAL has been found to trigger apoptosis and cause the loss of CNS neurons. Therefore, the synergic destructive effects of both DOPAL and DOPEGAL accelerates death of nerve cells, as seen in SIDS (sudden infant death syndrome), Alzheimer’s, Parkinson’s disease, and dysfunctional disorders of development and aging.

Overmasturbation resulted in Parkinson's symptom - restless or shivering legs and hands - due to abrupt drop of dopamine for excessive dopamine-neorepinephrine-epinephrine-DOPEGAL (3,4-dihydroxyphenylacetaldehyde) and dopamine-DOPAL(3,4-dihydroxyphenylacetic acid) conversion, leading to neurotoxicity and nervous death for no more sexual orgasm
==> http://www.actionlove.com/cases/case15611.htm

MAO, the brain/nervous and liver enzyme,  exists virtually in all mammalian cell types, with the notable exception of the erythrocyte. Excessive monoamines such as dopamine, norepinephrine and epinephrine induced by chronic stress, excessive sexual stimulation and orgasm and/or drugs will activate the liver Cytochrome P450 and MAO for oxidization (deamination) and detoxification, as described above, in order to maintain the homeostasis of the brain and nervous function. But, unfortunately, the resulting toxins destroy or damage the local neurons or synapses. In humans, there are two types of MAO: MAO-A and MAO-B. Both are found in neurons, hypothalamus, cerebral cortex (conscious control center), cerebellar cortex, pons, medulla oblongata, substantia nigra, caudate, astroglia, skins, and skeletal muscles.  Outside the brain and central nervous system, the liver, gastrointestinal tract , adrenal glands, kidnes, heart, lungs, and placenta have about 60-90% MAO-A and 10-40% MAO-B, but, MAO-B is mostly found in blood platelets. MAO's are enzymes that catalyze the oxidation of monoamines. They are found bound to the outer membrane of mitochondria in most cell types in the body. After placenta, liver contains the highest level of MAO, followed by kidneys, adrenal glands, heart, hypothalamus, substania nigra, lungs, intestine, caudate, medulla oblongata, pons, cerebral cortex and cerebellar cortex. That is, the liver, kidneys, adrenal glands, heart,  hypothalamus and substania nigra are likely aged or damaged by the  MAO-deaminated or oxidized toxins DOPAL, DOPEGAL, hydrogen peroxide (H2O2) and 5-Hydroxyindoleacetic acid (5-HIAA, as discussed below) faster than the other organs, and the liver will be damaged first. 
The main substrates of MAO-A include dopamine, serotonin, norepinephrine, epinephrine, octopamine, tyramine and tryptamine; the main subtstrates of MAO-B include dopamine, phenylethylamine, beta -phenylethylamine (PEA),  benzylamine, MPTP (1-methyl 4-phenyl 1,2,3,6-tetrahydropyridine),  tyramine, and tryptamine. 
MAO plays the key roles in the development of neurodegenerative disease,  including not only its putative role in converting an exogenous protoxin to a toxin, as mentioned above, but also its role in the formation of peroxides generated from the oxidative metabolism of dopamine.  MAO catalyzed deamination of dopamine to DOPAL and production of hydrogen peroxide (H2O2) and ammonia NH3 depend on concentrations of dopamine within the cytoplasm. Hydrogen peroxide, if not detoxified by glutathione peroxidase, can be converted by iron-mediated Fenton reactions to toxic hydroxyl radicals ( -OH) that induce lipid peroxidation and cell death. In addition, excessive ammonia accumulation in the bloodstream, termed as hyperammonemia,  can cause the confusion and coma of hepatic encephalopathy as well as the neurologic disease.     On the other hand, MAO-A breaks down serotonin into 5-Hydroxyindoleacetic acid (5-HIAA) and steals serotonin from arylalklamine N-acetyltransferase (AANAT), resulting in depleting the melatonin synthesis. Melatonin plays the key role for the mechanisms of circadian rhythm for healing the damaged cells while 5-HIAA is responsible for the developments of certain tumors or cancers.  Graveyard workers are at risk due to hyperactivities of MAO.  Our product DeToxiA, MoodMax, ViaGrowth-IV, PinealTonin and ArgiNOx have been formulated  to help you reduce the MAO gene expression
(or weaken the MAO activities in the dopamine, serotonin, norepinephrine and epinephrine nervous terminals) and hydrogen peroxide (H2O2)  formation, and enhance the liver urea cycle to remove ammonia NH3 from the blood stream (that is, detoxification of the nervous system, liver and blood!)
Most recent studies also indicate there is significant positive correlations between platelet MAO activity and cortisol measures. In normal sexual activities, orgasm or ejaculation is supposed to drop the cortisol level and to elevate norepinephrine and epinephrine level. If MAO turns serotonin into 5-HIAA and depletes serotonin production during or after sex, the post-sex elevation of norepinephrine and epinephrine will activate the MAO action on the adrenal cortex for excessive cortisol elevation several hours after the cortisol drop induced by ejaculation or orgasm.  Cortisol overshooting suppresses the adrenal DHEA production and testicular function, resulting depletion of androgen hormones in the brain,  and then causes post-sex hangover,  memory loss and depression in the next few days.  Maintaining a high level of cortisol will suppress immune function, promote atherosclerosis, and damage and kill brain cells eventually.  Excessive sex, orgasm or ejaculation, or/and drug abuse for pleasure rewarding or/and sexual enhancements can let you experience both hypocortisolism and hypercortisolism in your daily life when the cortisol diurnal rhythm is disturbed or the cortisol level is too low in the certain time of a day, but becomes over-shooting in the other time.  The complicated symptoms induced by sexual practices was named as Sexual Exhaustion Symptoms by Dr. Lin, as given in http://www.actionlove.com/cases/case9848.htm.

With an exhausting hypothalamus-pituitary-adrenal axis, patients may experience some of hypocortisolism symptoms during sex or in couple hours after sex, followed by some of hypercortisolism symptoms  several hours or in next days after sex. This will puzzle your medical doctors.

2. Sex-induced excessive inflammatory hormone prostaglandin E2 production, due to the excessive excitory neurohormones and the deficiency of androgen hormones (due to the disabling of the testicular and ovarian function by an excessive, persistent prolactin elevation at about 2-4 hours after orgasm/ejaculation):  In this regard, prostaglandin E2 induced body pain or inflammation originally serves as a warning sign of excessive sex.  If you ignore the warning signal, prostaglandin E2 will eventually give you more, including  inflammation responses, cellular multiplication, nervous excitation (for androgen hormone production (the good), inflammatory orgasm (the bad) and persistent sexual arousal (the ugly)), nervous exitotoxcity and immune suppression.  Persistent action of prostaglandin E2 on a cell will eventually alternate the cellular gene for potential cancerous or tumor development.

In addition, excessive sex or/and drug abuse also alternate the functions of the hypothalamus-pituitary-adrenal axis (HPA) and the sympathetic adrenomedullary system.  In addition to body pains and inflammation, our readers have also reported sex-or drug-induced memory loss, absent mindedness,  no concentration, less focusing,  hangover, or pseudo-Alzheimer's symptoms.  These problems can be associated with an overshooting of cortisol. In the normal condition, the sexual activities should not increase the cortisol level unless sexual arousal or orgasm induces inflammation; instead, normal sex tends to slightly reduce the cortisol level for activation of the pituitary-adrenal and -testicular function during and after sex.   In some case, the cortisol level drops too low, low enough to activate the inflammatory factors, leading to sex-induced pains , cramps or headaches while the norepinephrine and epinephrine level shoot up or remain too high. During sexual arousal, if the cortisol level shoots up (Note:  prolonged exercises overshoot cortisol, epinephrine, norepinephrine, Glucagon and growth hormones at the same time for a hyper-sympathetic nervous Fight), the prolactin level will follow; the man will go limp and the women will becomes dry; the lovemaking couples will experience sympathetic nervous Flight responses and the sexual arousal will be terminated. The release of cortisol, from the adrenal cortex,  is supposed to suppress the activities of the pro-inflammatory factors induced by an elevation of epinephrine, norepinephrine or/and histamine when the hypothalamus-pituitary-adrenal axis (HPA) responds to sexual arousal,  orgasm, masturbation, ejaculation, stress or drugs.   Under chronic loading of sexual arousal,  orgasm, masturbation, ejaculation, stress or drugs, the HPA can respond in 2 ways:  either abruptly dropping cortisol or excessively releasing cortisol.  If the adrenal cortex  released insufficient cortisol, the patients will experience immediate shape pain or mood change when the epinephrine, norepinephrine or/and histamine level overshoot out of the normal range.  

Under adrenal fatigue or deficiency conditions, the patient can experience the deficiency of both cortisol and androgen hormones (DHEA, testosterone or DHT), leading to persistent and severe body pains or inflammatory responses.

On the other hand,  if the adrenal cortex persistently shoot up the cortisol level and keep it high, the patient will experience foggy brain, memory/contraction/focusing loss, sleeping disorder,  and hangover in next few days. If either prolactin or cortisol level maintains too high, high enough to slow or shut down the adrenal and testicular function, leading to deficiency of DHEA, androstenedione, testosterone or/and DHT,  the patient will also experience post-sex inflammatory body pains, cramps or muscular rigidity due to excessive prostaglandin E2 production as a warning sign. The inflammatory responses usually occurs in few hours and the next day when the DHEA, androstenedione, testosterone or/and DHT are used up and drop down to deficient levels, too low to suppress the pro-inflammatory responses induced by excessive epinephrine and/or, norepinephrine.  
A chronic elevation of cortisol in the cerebrospinal fluid will cause depression and memory loss since cortisol can shrink or atrophy the hippocampus, associated with many kinds of memory and learning.  Unfortunately, under the conditions of chronically excessive sex/orgasm or over-masturbation/over-ejaculation, prolonged stress or drug abuse, excessive release of epinephrine, norepinephrine or/and histamine will open the brain-blood barrier (BBB) for more cortisol and other toxins to cross the BBB to pollute the cerebrospinal fluid and then to shrink the hippocampus,  like the elderly people experience.

Memory, brain and nervous functions can be also associated with Phosphorylcholine, a molecule mainly secreted by the seminal vesicle.  But, Dawson also reported that phosphorylcholine can also be found in the rat liver, testicles, spleen, intestines, kidney and brain, but there is only trace amounts in muscles, heart and blood, as given in http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1215699 and http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1215984.  More recently, it was found that the phosphorylcholine synthesis also occurs in the photoreceptors in supporting the eye visual sensing system (for example, http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=348559&blobtype=pdf ).  Phosphorylcholine combines with ceramide through a phosphodiester bond to create sphingomyelin, an important compound in the formation of the myelin sheath. Stroke victims and Alzheimer patients have shown improvement by increasing the phosphorylcholine level. In rat studies, tissue examination showed that phosphorylcholine was able to help repair damaged neurons. Phosphorylcholine was also found to help prevent a drug-induced drop in acetylcholine levels and improve memory and cognitive function ( http://www.fasebj.org/cgi/content/full/14/14/2198 ).  Over-ejaculation or excessive orgasm burns out, interrupts or discharges excessive phosphorylcholine and may let you experience poor memory or concentration and visual disorders.  I suspect that the depletion of phosphorylcholine synthesis induced by excessive ejaculation or orgasm, in conjunction with neuroexcitotocity of glutamate/norepinephrine/epinephrine and monoamine oxidization toxins (3,4-dihydroxyphenylacetaldehyde(DOPAL), 3,4-dihydroxyphenylglycoaldehyde (DOPEGAL), hydrogen peroxide (H2O2) and 5-Hydroxyindoleacetic acid (5-HIAA)), its resulted excessive release of  prolactin/cortisol and prostaglandin E2,  and its resulted deficiency of androgen hormones, leads to premature onset of Alzheimer's and Parkinson's disease, brain/nervous damage, liver/spleen/digestive/testicular disorders, cardiovascular disorders, and poor vision.  
Note:
Semen has high concentrations of potassium, zinc, calcium, magnesium, citric acid, fructose, phosphorylcholine, spermine, prostatic acid phosphatase, free amino acids, prostaglandins and enzymes, which nourish and protect the sperm.  Due to the high concentration of Phosphorylcholine in semen, the old Taoists theorized that men can return semen (actually phosphorylcholine) to revert the brain. Generally speaking, the concept is correct; however,  when the brain's dopamine or testosterone level is too high for excessive semen production, you still have to ejaculate to burn the dopamine and testosterone and to induce the prolactin release in the pituitary and retina for some protective and anti-inflammatory hormone 16K-prolactin to cool down the nervous systems, so that you can avoid the side effects of excessive dopamine or testosterone.  In this way, you can benefit from sex. Note that testosterone and acetylcholine can excite the dopamine-hypothalamus-pituitary axis and oxytocin release for sex.
Futhermore, Semen contains a lot of GABA ( http://www.andrologyjournal.org/cgi/content/full/25/1/140 , http://www.ncbi.nlm.nih.gov/pubmed/6237538?ordinalpos=1&itool= EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstractPlusDrugs1 ) and beta-endorphin http://www.ncbi.nlm.nih.gov/pubmed/6291653?ordinalpos=1&itool= EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstractPlusDrugs1 , http://www.ncbi.nlm.nih.gov/pubmed/2216060?ordinalpos=8&itool= EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum), both of which are the calm/inhibitory neurochemicals.  For a healthy man, ejaculation triggers glutamate-GABA conversion with the liver enzyme glutamate decarbozylase while glutamine is converted to glutamate by the liver enzymes glutamate synthase and synthelase.  In a male rates model, the cerebrospinal fluid(CSF)'s GABA and Asparagine/glutamate concentration increases 1000% and 200%, respectively, and there is a small decrements in amino accids such as serine, arginine, Alanine and leucine ( http://www.ncbi.nlm.nih.gov/pubmed/2877423?ordinalpos=4&itool=
EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum. ).  If there is a lack of  the liver enzyme glutamate decarbozylase, glutamate in CSF becomes too high and GABA becomes too low. This is why ejaculation causes deficiency of GABA and excessive glutmamte for the brain and nervous instability and sympathetic nervous Fight or Flight responses. Semen's GABA and beta-endorphin in the vaginal and cervix can block the female dopamine, oxytcoin and glutamate nervous excitation in the brain via the pituitary-uterus/cervix vagal nervous pathway, Both GABA and beta-endorphin also increase the female cerebrospinal fluid's GABA and beta-endocrine concentration right after male ejaculation, leading to calming the female central nervous system and reducing the oxytocin release. That is why premature ejaculation will disable libido immediately, unless the semen's prostaglandin E2 and glutamate can continue exciting the clitoral, G-spot, cervix and uterus vagal nerves. However, semen/CSF's GABA and beta-endorphin can help male and female post-orgasm pains in the urethra, prostate, bladder, clitoris,  vagina, uterus, and tailbone http://endo.endojournals.org/cgi/reprint/145/3/1331. Note: Beta-endorphin is mainly produced by the hypothalamus-pituitary-adrenal and -testicular/Ovarian axis in response to stress.  A sexual exhaustion person will fail to release sufficient beta-endorphin in help suppress pains.  A persistent sexual arousal person lacks of GABA and beta endorphin, but has a high level of glutamate, dopamine, norepinephrine, epinephrine and/or histamine.  Obviously, a person with a lack of serotonin, GABA and beta-endorphin will experience severe anxiety, depression, mood swing, de-realization, irrational thinking, irritation, panic responses, premature ejaculation, penile or clitoral over-sensitivity, and pains.   

Therefore, excessive sex or/and drug abuse result in multiple, sexual exhaustion symptoms which become UFO for western doctors and medical societies, although the Chinese Sex Bible and medicine documented them 5000 years ago.
==> http://www.actionlove.com/cases/case15448.htm
Why great sex life can result in divorce and end his sex life with low libido and headaches.
==> http://www.actionlove.com/cases/case15717.htm

On the effect of ejaculation on the testosterone production and aggressiveness or mode swing. Why it will take about 7 days to release the post-ejaculation or post-orgasm sexual exhaustion symptoms
http://www.actionlove.com/cases/case15719.htm

Warning: Pornography is a dirty bomb that can blast your mind, body and soul away, that is, kills your brain by excitotoxicity!  And,  SEX is a most strange, addictive drug without ingredients, in the name of love. Sex overdosing is an extremely destructive self-destruction, but unfortunately you will die for it (you become addictive to sex, due to the brain/dopamine nervous plasticity or the prostaglandin E2 induced persistent sexual arousal)!!!!!  When you have sex overdosed, your brain's acetylcholine, dopamine, serotonin and GABA nervous systems are burned out (ok, Dr. Lin called it the nervous excitotoxicity), your hypothalamus-pituitary-adrenal and testicular (ovarian) axis are partially or fully disabled,  your blood and cerebrospinal fluid chemistries are changed with a chronic elevation of epinephrine, cortisol, prolactin and prostaglandin E-2 for sexual exhaustion symptoms and sympathetic nervous fires (anxiety, stress, mood swing,  hangover, sleeping disorders, Obsessive Compulsive Disorder (OCD), inflammatory pains (in the upper back, neck, rear brain, joints, pelvis, perineum, low back, vulva, clitoris, vaginapenis, testicles, urethra, prostate and stomach), parkinsonism,  memory loss, vision disorders, ear ringing, chronic fatigue, brain disorders, headaches, dizziness, migraines, vertigoinflammatorily persistent sexual arousal symptoms, ejaculation or post-orgasm pains or cramps,  and so on) with a lack of healing and restoration forces, even if you are female,  and your excessive "love" becomes a poison to your health!  Realistically, your organs are bathed in the "bad" blood and your brain and spinal nerves work under chemically- and hormonally-unbalanced cerebrospinal fluid very day!!!  It is expected that the cellular DNA/genes in the organs will be gradually changed for worse, accordingly. Your 20-year old body then become 60 years old!!!! And your doctorS can not help you out even if prescribing drugs to shut down your sexual function won't help. Your doctors may tell you that you have psychological or psychiatric disorders. Please don't consider suicidal.  We can help you out.

Ejaculatory Frequency and Seasonal Change vs Semen Quality: according to http://www.ncbi.nlm.nih.gov/pubmed/15302284?dopt=Abstract , Increasing your ejaculatory frequency will drop your sperm concentration, but there is no seasonal variations in sperm concentration, motility, or morphology. Compared with one ejaculation per week, sperm concentration fell 29% with two ejaculations per week, and by 41% with three ejaculations per week.  Noticeable, the spring ejaculatory frequency is significantly higher in spring months than the winter's.  Note:  the pituitary-testicular axis and the skin endocrine function respond to the seasonal temperature change, and more active in warm weather.

Ejaculation Frequency vs. Testosterone Level
1. http://www.ncbi.nlm.nih.gov/pubmed/12659241?dopt=Abstract - "The purpose of this study is to gain understanding of the relationship between ejaculation and serum testosterone level in men. The serum testosterone concentrations of 28 volunteers were investigated daily during abstinence periods after ejaculation for two phases. The authors found that the fluctuations of testosterone levels from the 2nd to 5th day of abstinence were minimal. On the 7th day of abstinence, however, a clear peak of serum testosterone appeared, reaching 145.7% of the baseline ( P < 0.01). No regular fluctuation was observed following continuous abstinence after the peak. Ejaculation is the precondition and beginning of the special periodic serum testosterone level variations, which would not occur without ejaculation. The results showed that ejaculation-caused variations were characterized by a peak on the 7th day of abstinence; and that the effective time of an ejaculation is 7 days minimum. These data are the first to document the phenomenon of the periodic change in serum testosterone level; the correlation between ejaculation and periodic change in the serum testosterone level, and the pattern and characteristics of the periodic change."  also in http://www.ncbi.nlm.nih.gov/pubmed/12506329?ordinalpos=2&itool=EntrezSystem2.PEntrez
.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum
2. 
http://www.ncbi.nlm.nih.gov/pubmed/11760788?dopt=Abstract - "This current study examined the effect of a 3-week period of sexual abstinence on the neuroendocrine response to masturbation-induced orgasm. Hormonal and cardiovascular parameters were examined in ten healthy adult men during sexual arousal and masturbation-induced orgasm. Blood was drawn continuously and cardiovascular parameters were constantly monitored. This procedure was conducted for each participant twice, both before and after a 3-week period of sexual abstinence. Plasma was subsequently analysed for concentrations of adrenaline, noradrenaline, cortisol, prolactin, luteinizing hormone and testosterone concentrations. Orgasm increased blood pressure, heart rate, plasma catecholamines and prolactin. These effects were observed both before and after sexual abstinence. In contrast, although plasma testosterone was unaltered by orgasm, higher testosterone concentrations were observed following the period of abstinence. These data demonstrate that acute abstinence does not change the neuroendocrine response to orgasm but does produce elevated levels of testosterone in males."
3. American population testosterone level dropped about 50 ng/dl for men at around age 64-65 between 2 groups of men born in 1920-1924 and 1930-1934, according to in http://jcem.endojournals.org/cgi/reprint/92/1/196. When the 1920-1924 group reached the median age 65, their mean testosterone level was 500 ng/dl; when the 1930-1934 group reached the median age 56 and 64, their mean testosterone was 529 ng/dl and 444 ng/dl, respectively. The 1930-1934 group has a testosterone drop rate at about 10.65 ng/dl per year during ages 56-64. This report also shows that the testosterone drop rate generally becomes faster for the men from 55 to 65. If we use the same annual drop rate of the 1930-1934 group, the extrapolated, averaged testosterone level of of 20 year old men born during 1930-1934 should be about 911 ng/dl.  Assuming that the mean 20-year old testosterone level for both groups are the same  is about  911 ng/dl, the overall-averaged testosterone drop for the 1920-1924 group is about 9.13 ng/dl/year, while the overall-averaged testosterone drop for the 1930-1934 group  is about 10.61 ng/dl/year  I suspect the higher masturbation/ejaculation frequency in the younger generation after the 60's sexual revolution resulted in a higher cortisol/ prolactin level (or faster ageing of the hypothalamus-pituitary-adrenal and -testicular axis) accelerates the testosterone drop, since some high-frequency over-masturbation young men experience male menopause (andropause) between ages 20-30. 
4. Our observations for healthy ejaculation frequency (or refraction times) vs age, in order to maximize the testosterone level, are:
  1. 4-7 times per week for teenagers of age 16-19.
  2. 3-6 times per week for young men of age 20-25.
  3. 3-5 times per week for young men of age 25-30.
  4. 2-4 times per week for men of age 30-45,
  5. 1-3 times per week for men of age 45-60,
  6. 1-2 times every 10 days for men of age 60-70.
  7. No more than once a week days after age 70
 Lovemaking orgasms stimulate the pituitary to release oxytocin for a faster recovery; while masturbation may not help the pituitary to release enough oxytocin. Therefore, the masturbation ejaculation frequency should be limited to the low limit as possible as you can. If your ejaculation orgasm produces sexual exhaustion symptoms,  your ejaculation frequency should be lower than the listed above.  The actual ejaculation frequency is associated the refraction (recovery time) of the hypothalamus-pituitary-adrenal, -thyroid and -testicular axis. The energetic time (full recovery with powering up) for a man having a morning (8 AM)  testosterone level at 350-400 nd/gl is about 7 days when his testosterone level reach its peak, over 500 ng/dl. If he keeps this ejaculation frequency, he will likely maintain his testosterone level around 450-550 ng/dl, thereafter. A man with a high testosterone level of 700 ng/dl or higher can re-erect  the penis in a few minutes after ejaculating if his pituitary doesn't overshoot his prolactin level, but it doesn't mean he can ejaculate again.  This is because the ability of penile re-erection can be associated with the dopamine nervous action on the pituitary oxytocin and prolactin release and the stimulation of testosterone, nitric oxide, prostaglandin E1 and  prostaglandin E2 stimulation on the prostate and penile erectile nerves.  Prostaglandin E2 can re-erect the post-ejaculating penis again when the oxytocin level is high and the prolactin level is not overshooting out of the range. The prostaglandin E2 induced erection usually accompanies a little pains in the prostate, urethra and penis. Even if you can re-erect your penis for sex again,  the post-ejaculation elevating cortisol and prolactin will start to lock up the adrenal and testicular function to drop your DHEA and testosterone production few hours after the first ejaculation. 

Sex as a Drug: Over-Masturbation at 20-25 times a day since age 7, masturbation addiction, masturbation withdrawal symptoms, and brain damage turned a gifted kid into a stupid junkie
http://www.actionlove.com/cases/case15605.htm
The destructive testing results of over-masturbation from a 17-yearo-old boy - sexual exhaustion symptoms for no more life and sexual orgasm, including, body pains, arthritis, testicular pain, penile pain, prostate pain, back pain, face pain, gum pain, tinnitus (excessive glutamate and inflammatory hormone prostaglandin E2), headcahes, fatigue, anxiety, nightmare, chilliness and shivering attacks, hot flashing/fever (premature male menopause), cracking joints, fibromyalgia, impotence, Restless Leg Syndromes (pre-parkinson's disease) and so on.
==> http://www.actionlove.com/cases/case15655.htm

FDA Warnings: 
News Upadated (July 8, 2005): All the erectile PDE5 inhibiting drugs can cause sudden decreases or loss of eyesight (even blindness, under a very fancy name "Nonarteritic Anterior Ischemic Optic Neuropathy (NAION)", as warned by the US FDA in in -
http://www.fda.gov/cder/drug/InfoSheets/patient/sildenafilPIS.htm 
http://www.fda.gov/cder/drug/infopage/cialis/default.htm or http://www.fda.gov/cder/consumerinfo/viagra/default.htm
http://www.fda.gov/cder/drug/InfoSheets/HCP/sildenafilHCP.htm  or http://www.pbm.va.gov/alerts/PDE5.pdf 
News Upadated (Oct. 18, 2007): All the erectile PDE5 inhibiting drugs can cause sudden decreases or loss of hearing, tinnitus and dizziness as warned by the US FDA in http://www.fda.gov/medwatch/safety/2007/safety07.htm#PDE5.  

In fact, Dr. Lin has documented the sex-induced nervous disorders since 1997 in our websites,  although these problems were well-addressed in the Chinese Sexual Bible "Suu-Nu Ching" and Medical Textbook "Yellow Emperor's Classic of Internal Medicine" around 2600 B.C..  Realizing the sexual exhaustion systems, Dr. Lin has developed the ViaPal-hGH formulas and other products to help you rejuvenate your exhausted brain/nervous and endocrine functions for health and then sex. Dr. Lin has also addressed the optimal, safe sexual/orgasm frequency for the different age groups of people without damaging the brain and neuro-endocrine system.
Health Canada Warning - http://www.hc-sc.gc.ca/ahc-asc/media/advisories-avis/2005/2005_83_e.html.
So, you should read this link about sex and vision too before taking erectile drugs -
http://www.actionlove.com/extra/eyefloater.htm,  but don't have to die for SEX! 
The Root of Over-Masturbation/Excessive Sex:
 

Male/Female Persistent Sexual Arousal Syndrome - http://www.actionlove.com/extra/psas.htm
Penile Enlargement Updated: The role of DHT, prostaglandins E-1/E-2/E-3, and Nitric Oxide in the penile enlargement for more sexual orgasm (Here is the fact: A balance action of prostaglandin E-1 and E-2 on the nerves and blood vessels allow the tissue to expand and stretch without pains. For example: pregnant women stretch and grow the uterus and abdomen without pains under a simultaneous, balanced action of prostaglandin E-1 and E-2,  but start labor contraction pains when prostaglandin E-2 overpower prostaglandin E-1, in conjunction with the action of oxytocin, cotisol and epinephrine!)
http://www.actionlove.com/cases/case13917.htm
 
Natural Vaginal Rejuvenation and Tightness Updated: ballooning of the vaginal spongy tissues, G-spot erectile tissues, corpus cavernosum clitoridis, and vestibular bulbs will tighten up you vaginal orifice and canal. For detail please go to http://www.actionlove.com/extra/vsize.htm 
The basic principle of the penile and clitoral/G-spot ballooning is to turn the local skin into an endocrine organs for more DHEA,  DHT, testosterone, and prostaglandins production to feed the erectile tissues and nerves, as described in
http://www.fasebj.org/cgi/reprint/04-1968fjev1
and
http://edrv.endojournals.org/cgi/reprint/21/5/457

Excessive Sex for dark eye circles, nips, labia minors, pelvic area, perineum clitoral/penile forskin:   Skin is a neuroendocrine organ. Chronic stimulation of sex organs can lead to over-production of α-MSH and Trapping excessive α-MSH in certain areas of skin results in extra skin darkness, particularly in eye cycles, nips, labia minors, penile and clitoral foreskin, and perineum if the local skin neuroendocrine function was working, but the local blood circulation becomes poor due to excessive noepinephrine or epinpehrine binding in the sympathetic andrenergic-α2 receptors of the blood vessels or a lack of nitric oxide and prostaglandins E1/E3 in the local tissues .

Benefits from Optimal Orgasms (the Tao of Sexual Orgasms): Orgasm triggers the pituitary to release prolactin. Although chronically excessive prolactin can disable the sexual function, induce cancerous development, screw up the reproduction system and cause depression, an optimal prolactin release from your pituitary and eyes, as a result of an orgasm, is good for hGH production, cancer and tumor prevention and for healthy eyes, brain, heart, liver, kidneys, uterus and prostate. Particularly, if chondrocytes (bone marrow stromal stem cells) can release the enzyme matrix metalloproteinases to convert prolactin into 16K-prolactin (16 kDa N-terminal fragment of the hormone prolactin), you will benefit from the antiangiogenic effects from 16K-prolactin. 16K-prolactin can block the blood vessel invasion or new blood vessel growth, associated with the endochondral bone formation (blocking mitogen-induced vascular endothelial cell proliferation, involved activation of programmed cell death) and tissue repair after injury and inflammation (by prostaglandin E2!),  which is an important mechanism underlying human diseases such as cancer, diabetic retinopathy, rheumatoid arthritis, and heart diseases. It is antiangiogenic, but excessive 16K-prolactin inhibits the penile or clitoral growth, or other normal cellular or nervous repair and regeneration/rejuvenation.  Therefore, you need an optimal orgasm frequency to prevent cancers (including prostate cancers), tumors and retinopathy (non-inflammatory damage to the retina of the eye, due to lack of of the blood supply, damaged or constricted blood vessels. However, you should not have an excessive sex or orgasm since it will produce excessive stress hormones to inhibit the release of the enzyme matrix metalloproteinases, to suppress the neuro-immune system and to activate the inflammatory factors triggering your health alarm system, as a result of the excessive prostaglandin E2 production. The inflammatory factors actually damage the bone marrow cells. Due to the fact that semen contains high concentration of Phosphorylcholine essential to the brain and nervous function and repair, the old Taoists theorized that men can return semen (actually phosphorylcholine) to revert the brain. Generally speaking, the concept is correct; however,  when the brain's dopamine or testosterone level is too high for excessive semen production, your pituitary will be over-exited, leading to excessive oxytocin release and prolactin deficiency, in addition to neuroexcitotocity from dopamine-induced excessive glutamate and histamine production, the deamination of dopamine to DOPAL and the oxidative stress from the demination byproduct Hydrogen Peroxide.  Therefore, Optimal orgasm and ejaculation can help you burn some dopamine and testosterone out,  and then induce the prolactin release from the pituitary and retina tissues for some protective and anti-inflammatory hormone 16K-prolactin in cooling down the nervous systems. In this way, you can avoid the side effects of excessive dopamine or testosterone, and benefit from sex. That is, an optimal orgasm or sex can improve your health.
Remember this:
Bone Morrow and Sperms: Reuters (April 13, 2007) said Dr. Karim Nayernia at the University of Gottingen, discovered stem cells taken from the bone marrow of men may be able to transdifferentiate to sperm cells in 3-5 years - http://search.yahoo.com/search?p=Karim+Nayernia+sperm+marrow&ei=UTF-8&fr=moz2
The Traditional Chinese Medicine considered bone marrow is Essence (Jing) for semen production. What is a coincidence! This means that over-ejaculation or excessive orgasm will cost your bone marrow and weaken your bone. Other stem cells researches have done similar work in female mice and turned bone marrow cells into egg cells. What does this mean to women's body pains or arthritis?  This means excessive orgasm/sex/ejaculation, job-related stress, substance abuse or toxins can inhibit the enzyme matrix metalloproteinases from the bone marrow stromal stem cells.  This is why our readers kept reporting inflammatory pains and arthritis induced by orgasm/ejaculation,  job-related stress, substance abuse or toxins. 

As of today,  a high level of prolactin has been realized as a promoter or co-initiator of breast and prostate cancers, in addition to disable the sexual function. It appears to play a key role in the development and progression of breast and prostate cancer and tumors.  So, keep your prolactin level in the normal range and avoid the synergistically biological effects of the prolactin on the estrogen or/and DHT receptors.

You will get another benefit from sex and orgasm if you get a resulted elevation of both GABA and glutathione which are converted from excitototoxicity glutamate. GABA is synthesized from glutamate using the enzyme L-glutamic acid decarboxylase and pyridoxal phosphate as a cofactor, and glutathione from the amino acids L-cysteine, L-glutamate and glycine in two adenosine triphosphate-dependent steps:   by combining L-glutamate and cysteine via the enzyme gamma-glutamylcysteine synthetase to form gamma-glutamylcysteine, and then adding glycine to gamma-glutamylcysteine via the enzyme glutathione synthetase to produce glutathione. Elevation of GABA with serotonin, norepinephrine and prolactin after sex or orgasm will trigger the pineal gland and retina to release melatonin for better sleeping, hGH production, nervous regrowth, neuro-endocrine restoration, cellular repair,  and shaper vision;  Elevating of glutathione can reduce the formation of  oxidative toxins, such as Hydrogen peroxide (H2O2),  associated with oxidative injury and cellular/nervous damage.  However, if you lack of these liver enzymes ( L-glutamic acid decarboxylase, pyridoxal phosphate , gamma-glutamylcysteine synthetase and glutathione synthetase)  and amino acids L-cysteine and glycine, you will get excitotoxicity and brain/nervous damage from your orgasm sponsoring neurotransmitters glutamate, dopamine, norepinephrine, epinephrine and histamine which stimulate the gene over-expression of monoamine oxidase in your brain, liver, kidneys, adrenal glands, heart and other organs for premature ageing, brain and nervous damage,  and sexual exhaustion symptoms (as listed in http://www.actionlove.com/cases/case9848.htm).


Brain-Skin/Brain-Hair connection - the effect of excessive sex-induced stress on skin (acne) and hair (hair loss) !  

My case collection since 1997 is given in
http://www.actionlove.com/extra/acne.htm and
http://www.actionlove.com/extra/hailoss.htm 
My intention is to have a statistical data (cases) to support the traditional Taoism's and Chinese Medical claims about the side effects of over-sex on the acne outbreak and hair loss. In the past, there have been a lot of disputes on this issue (for example, please read http://answers.yahoo.com/search/search_result;_ylt=AlClvcr4x7agkfBvF65HS6Hpy6IX;_ylv=3?p=over+masturbation ).  Luckily, I also have found the scientific research support on these claims. Scientifically, it is called the skin's and hair-follicle's hypothalamus-pituitary-adrenal axis or the skin/hair stress response axis - the response of the body to acute and chronic stress induced by temporarily or chronic over-sex activities. Under acute or chronic stress, neurohormones, neurotransmitters, neuropeptides and neurotrophins will stimulate a series of adaptation responses, leading to behavioral, cardiovascular, metabolic, endocrine and immunological changes. The most critical one is the immunological changes ranging from immune suppression to imflammation. Acne, skin allergy,  and hair loss can be considered as a result of inflammatory diseases. In fact,  psychological stress causes more inflammatory and autoimmune diseases than what you think. I have termed the resuted diseases as the Sexual Exhaustion Symptoms  if they are directly or indirectly induced by sex-induced stress - chronic or acute! If you still don't understand why excessive stress induces acne and hair loss, you should read the following links-
http://edrv.endojournals.org/cgi/reprint/21/5/457 ,
http://www.fasebj.org/cgi/reprint/04-1968fjev1,
http://edrv.endojournals.org/cgi/reprint/21/5/457,
http://www.psychosomaticmedicine.org/cgi/reprint/63/3/412,
http://www.tufts.edu/sackler/pharmacology/faculty/theoharides/documents/TiI-brain-skin.pdf,
http://edrv.endojournals.org/cgi/reprint/22/4/502,
http://www.fasebj.org/cgi/reprint/19/10/1332,
http://ajp.amjpathol.org/cgi/reprint/165/1/259,
http://www.nature.com/jid/journal/v122/n1/pdf/5602146a.pdf,
http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=1868107&blobtype=pdf
and http://www.nature.com/jid/journal/v117/n2/pdf/5601158a.pdf

Excessive sex, drug/alcohol abuse, work overloads,  Over-eating (high-protein overdosing and high-tyramine foods), excessive caffeine intake, and excessive exercises can induce excessive stress hormone production for hair loss (actually, stopping hair regrowth after losing hair)  and acne outbreak - the sympathetic nervous fires in your skin and hair follicles. Sleeping disorders indicate excessive stress with insufficient serotonin and GABA nervous modulation on the pineal and retinal function.  Your acne and hair loss can also be associated with sleeping disorders.


Orgasm Brain Sex Pain?!! - Oops! Click the links in the left-handed side if you need our case collection since 1997.  Or read some interested cases below:

On Taoist's ejaculation frequency vs testosterone level and sperm concentration.; 5000-years Sexual exhaustion symptoms were also mentioned by the Seventh-day Adventist church; what is a consistence of old culture wisdoms!
==> http://www.actionlove.com/cases/case15675.htm
On Sexual Energy Exchange during intercourse for the Tao of Love -
He said 'I will continue to use your products for time to time and hang on to your words of wisdom.' on sexual energy exchange during intercourse for more sexual orgasm
==> http://www.actionlove.com/cases/case15578.htm
why ejaculation or sexual orgasm induced awful depression, anxiety, body pains (dull throbbing gallbladder and liver pain) for a few day - Solution
==> http://www.actionlove.com/cases/case15444.htm
Pot smoking and alcohol result in memory loss, eye floaters, upper abdominal/stomach pains (went to ER twice for MRI, scans, colonoscopy..), vaginal dryness, uterine cramp and pain, post-sex low abdominal (uterine) pain, allergies. sinus, puffy eyes, headaches, forehead tenderness and no more sexual orgasm
==> http://www.actionlove.com/cases/case15747.htm
What cause the post-ejaculation and post-orgasm pains, cramps, tightness, joint rigidity and muscle weakness for no more sexual orgasm
==> http://www.actionlove.com/cases/case15079.htm 
Sexual Hangover - Sex or orgasm induced headache, poor mentality, mood swings, dizziness and vertigo - solution for the severe side effects of sexual orgasm
==> http://www.actionlove.com/cases/case15010.htm
The similarity of between the penile jelq-induced damage and heart failure as a result of increased collagen synthesis for no more sexual orgasm - A special Penile Enlargement advice
http://www.actionlove.com/cases/case14906.htm
He said ' I am so incredibly grateful for everything you have done for me so far! My erection is back for good now, and what your miracle products did for my health remains truly without precedence. ViaPal-HgH-J helped me to rejuvenate my penile erectile nerves and revive my dead penis after a very severe penile injury, after I ruptured both of my spongy tissues with one of the jelqing/stretching exercises I had found on the internet.'  Re-grow Corpora Cavernosa and penile nerves, heal penile varicose veins, improve penile curvature, solve penile pains, stop precum, and restore libido and sexual orgasm.
==> http://www.actionlove.com/cases/case14677.htm
2-week Finasteride (5-alpha reductase inhibitor for Hair ReGrowth and shrinking the enlarged prostate ) disabled his liver 5-alpha reducatse release in blocking the testosterone-DHT conversion for a high testosterone level, but administration of aromatase inhibitor supplements, in conjunction with the side effect of Finasteride, further kept his testosterone level too high, high enough to stimulate the excessive liver SHBG protein release in binding testosterone in the bloodstream for penile shrinkage, no more libido and sexual orgasm
==> http://www.actionlove.com/cases/case14664.htm
Why drug abuse and antidepression drugs result in excessive prostaglandin E-2 and epinephrine release to induce psychological disorders ( mood swing, anger, and aggression), extremely headaches, shooting pains low stomach swelling, body pains, body heat, light headedness confusion, uncontrollable over-masturbation (persistent sexual arousal), particularly during ovulation, for no more sexual orgasm
==>http://www.actionlove.com/cases/case14644.htm
Chronically over-masturbating for 2.5 years  resulted in low back pain, testicular pains, groins pains, urethral/penile pains, erectile dysfunction, painful erection, chronic constipation and elevation of the liver enzymes LST and AST (liver damaged index enzymes) for no more sexual orgasm, but pains.
==> http://www.actionlove.com/cases/case14451.htm
Why a hard core body builder or athletic person experiences penile and testicular shrinkage even if he is taking a lot of Nitric Oxide enhancements; on the role of the sympathetic nervous beta receptors in the penile erection, testicular function and sexual orgasm (the same conditions apply to women's clitoral/G-spot erectile dysfunction, vaginal looseness, and ovarian functional disorder too)
==> http://www.actionlove.com/cases/case14402.htm
His and her post-orgasm sexual exhaustion symptoms - sympathetic nervous panic and inflammatory responses, low back pains, low abdomen pains/cramps, perineum inflammatory pains, and so on, for no sexual orgasm - solution
http://www.actionlove.com/cases/case13819.htm
Why ejaculation/orgasm causes his mood swing, anger, aggression, anxiety, stress, fatigue, tiredness.... for no more sexual orgasm -  On the brain and body chemistry change in response to ejaculation or orgasm.
==> http://www.actionlove.com/cases/case13755.htm
He said ' I want to thank you because your products worked as you say they will and the value I got from them went beyond what I expected.' with ViaPal-hGH-J, DeToxiA and PinealTonin in detoxification of anti-psychotic and bipolar medication drugs for restoration of normal erection and sexual orgasm.
http://www.actionlove.com/cases/case13900.htm
She said ' a couple months ago I wrote to you about my problem with vestibulitis. your prescribed that i take vial pal hgh j along with borage oil, fish oil, and 5-htp. ... my doctor, who is one of the few vulvodynia and vestibulitis specialists in the country, is amazed by my rapid progress.' for solving vestibulitis, quitting pot smoking and restoring sexual orgasm.
==> http://www.actionlove.com/cases/case13584.htm
Solution for Persistent Sexual Arousal Syndrome and interstitial cystitis induced by COX-2 over-expression and inflammatory hormone prostaglandin E-2 in the pelvic cavity tissue and for control of unwanted, spontaneous sexual orgasm
http://www.actionlove.com/cases/case13532.htm
Non-orgasmic semen retention is as bad as over-ejaculation; both are for no more sexual orgasm ,but for sympathetic nervous pains and burning. What is different between both cases in term of the dopamine-norepinephrine-epinephrine conversion?
==> http://www.actionlove.com/cases/case13176.htm
He said 'I want to thank you for your products. I cannot begin to tell you how great it was for us to be able to have her squirt, and boy did she. I had no idea of the quantity of fluid that would come out or how forceful the ejaculation would be, I know for a fact that the movies that I have seen are indeed real!!!' with Heat Tea and L-Arginine! A realistic experiment for a healthy female ejaculation pumped out by an extremely powerful sexual orgasm!
http://www.actionlove.com/cases/case13138.htm
Why his doctors and drugs can not solve his non-organic prostate and testicle pains as a result of sexual exhaustion and prostate abrasion for no more sexual orgasm
http://www.actionlove.com/cases/case13121.htm
He said 'The chikong breathing worked! I thought your site was just after my money, but when I tried your advice my control over ejaculation was exactly like you said. The ballooning trick also worked and I was able to control (for the first time in my life) as long as I wanted' for  more sexual orgasm
http://www.actionlove.com/cases/case13080.htm
He said 'Your medium dosage of (MoodMax, 5HTP + Dopa Fibra, Dopa Fibra, MoodMax) has been great.'  for more sexual orgasm. How to shut down and boost your oxytocinergic nervous action for control of libido, erection and  sexual orgasm.
http://www.actionlove.com/cases/case13040.htm
Chronic over-masturbating from age 14-31 results in all of the sexual exhaustion symptoms, some fatigue, graying of hair, hair thinning, eye floaters, sinus, ear aches, and sleeping disorder for no more sexual orgasm. On the arylalklamine N-acetyltransferase gene expression disorder in the pineal gland and retina for circadian rhythm and visual nervous disorders. Why can a good sex improve your health?
http://www.actionlove.com/cases/case12909.htm
She said ' i am glad to notify you that it's unbeleavable how i have managed to get almost all my problems eliminated.as of now',  no more depression, hypertension, painful periods due to fibroids, migraine headache, vaginal muscle weakness, urinary sensation reaction, nausea, chronic sinuses, painful nipples, and low libido, but for sexual orgasm; on the pineal gland gene expression disorder.
==> http://www.actionlove.com/cases/case12813.htm
Over-ejaculating several times in 20-50 minutes have abraded his prostate and elevated a high PSA release for many days - for self destruction and no more sexual orgasm!
http://www.actionlove.com/cases/case12785.htm
ViaPal-hGH-M and DeToxiA have helped her resolve her chronic bladder disorder/ incontinence, vulva pain (Vulvodynia & vestibulitis ) & throat infection (tonsils), restore her menstrual cycle, and smooth out her PMS Pains/Cramps, for restoration of sexual orgasm
==> http://www.actionlove.com/cases/case12703.htm
Chronic over-masturbation/over-ejaculation or excessive orgasm alternates the Dopamine D1 and D2 gene expression for sympathetic nervous fires - no sexual orgasm - the brainwash solution..
http://www.actionlove.com/cases/case12612.htm
The cellular biochemistry of premature ejaculation for no more sexual orgasm.
==> http://www.actionlove.com/cases/case12610.htm
How to treat pot smokers' common problems for restoration of sexual orgasm
==>http://www.actionlove.com/cases/case12583.htm
Why his penile stretching enlargement exercise for 2 days results in youth (teenager's) impotence, glans shrinkage, premature ejaculation and low libido for no sexual orgasm
==> http://www.actionlove.com/cases/case12560.htm
A senior medical student said ' I have already been taking ViaPal-M for around 2 1/2 weeks and I must say that the results have been significant improving my symptoms of anxiety, poor memorization, acne, depression, etc. ' for sexual orgasm, and questioned on medication drugs for psychological and physiological disorders.
http://www.actionlove.com/cases/case12529.htm
Why this 20-year old man experiences orgasmic dysfunction and  withdrawal  for no sexual orgasm. On the role of prolactin and oxytocin in the sexual and orgasmic functions and in the switching of sympathetic nervous beta and alpha receptors for orgasmic contraction for men and women.
==> http://www.actionlove.com/cases/case12488.htm
Chronically masturbating twice a day lets her feel sexually unfulfilled, crave for more sex, and experience cramps in the low abdomen and back for sexual exhaustion symptoms, but no sexual orgasm. On the physiology and psychology of orgasm
==> http://www.actionlove.com/cases/case12487.htm
Dr. Lin's advices to a porn actor: Avoid multiple ejaculation in one day; Knock out all your partners with one and only one ejaculation for the most violent sexual orgasm by rhythmically stimulating the clitoris and blending the G-spot and Epicenter/cervix at the same time; Drink your own first morning pee - the Natural Spectrum Hormone Therapy.
==> http://www.actionlove.com/cases/case12460.htm
Chronic Over-masturbation causes a chronic elevation of prolactin for seminal / sperm production disorder, low libido, orgasmic disorder for infertility and no more sexual orgasm!  Why?
http://www.actionlove.com/cases/case12388.htm
Over-masturbation/over-ejaculation and drugs abuse killed his brain and nervous functions for chronic headaches, blurred vision, ear ringing and no more sexual orgasm. Here is Dr. Lin's Brainwash Engineering treatment.
http://www.actionlove.com/cases/case12366.htm
Over-masturbation has alternated and exhausted this 19-years old boy's brain/nervous functions for pains in the testicles/penile/groins/low abdomen/low back/everywhere, eye floaters and  suicidal thought for no more sexual orgasm, beyond ability of his psychologist and urologist and SSRIs antidepression drugs. The brain/nervous function destructed by over-masturbation or over-ejaculation can not be healed naturally! Here is Dr.Lin's cheap 'Brainwash' solution.
http://www.actionlove.com/cases/case12364.htm
After he spent all his money, why all his doctorS and all the prescription drugS can have never solved his non-bacterial prostatitis and prostate swelling with frequent urination, perineum heat/pains, and hair loss, leading to no more sexual orgasm - Here is Dr. Lin's cheap solution - The Natural Prostaglandin E-1 therapy.
==> http://www.actionlove.com/cases/case12346.htm
He said ' I have purchased your ViaPal-hGH-J pack and have been very happy with the results with an improvement after only 2 weeks.' how to balloon your penis and her clitoris/G-spot/vaginal/urethral erectile tissues for more sexual orgasm!
==> http://www.actionlove.com/cases/case12339.htm
Why his optometrist can not see his eye floaters resulting from over-masturbation/over-ejaculation or excessive sexual orgasm
==> http://www.actionlove.com/cases/case12334.htm
He said ' I have sexual functioning again.' with ViaPal-hGH-P; Re-Grow his circumcised foreskin, enlarge his penis, restore his orgasm and penis sensitivity after jelqing damage,  and shrink his enlarged prostate back to normal for peeing, and solve his urinary tract infection (UTI) for  more erection and sexual orgasm.
==> http://www.actionlove.com/cases/case12265.htm
Finally, a 21-year old  heavy-duty pot-smoking, post-hernia-operation over-masturbator said ' my urinary incontinence is absolutely GONE AWAY...  Thanks for your great product Dr.Lin !!'  Restoring his sexual orgasm in only 1 month!
http://www.actionlove.com/cases/case12201.htm
[Warning: This article may be very offensive to you, but you can learn about the relationship between the penile/vaginal temperature and orgasmic response, and the relationship among the urogenital blood circulation, urinary continence, androgen hormones and prostaglandin E-1. For a better sex, keep your penis/clitoris/vagina hot, but your brain cool; that is, pump your blood down to your sex organs, but not to your brain during lovemaking!  Their sexual adventures in helping us cross-verify our long-term hypotheses should be highly appreciated! OK, Here we go for it:
After her husband failed to maintain his erection for her, she is interested in dog sex for sexual orgasm. Can she have a dog tie? Dr. Lin's saddest advice! Updated (3/17/2004): She had experienced powerful multiple orgasms with the high-temperature dog penis and semen (3 degrees F higher than the human's). The result of the Dog Sex experiments can lead to a new powerful therapeutic concept for urinary incontinence! Why?
==> http://www.actionlove.com/cases/case12137.htm]
Dr. Lin's penile growth theory and permanently penile enlargement for you to go all the way to heaven and to have more sexual orgasm after you die.
http://www.actionlove.com/cases/case12121.htm
How urethral female ejaculation occurs and produces pelvic/bladder/urethral/vagina/uterus spasms and legs shaking (a temporary Parkison's phenomenon by sexual stimulation) , but no sexual orgasm; on the formation of  the sensory-sympathetic L1/L2 nervous reflex arc.
==>http://www.actionlove.com/cases/case12082.htm
He said ' i have been purchasing your products for about 4 months now for my wife. and they have helped a great deal!' for her Interstitial Cystitis (IC), fibromyalgia, migraine headaches, sleeping disorder, vaginismus (penetration/intercourse pains) and restoration of sexual orgasm - This serious case has been abandoned by the medical societies.
==> http://www.actionlove.com/cases/case12046.htm
Ear ringing (Tinitus) - the ear stresses out for no sexual orgasm
==> http://www.actionlove.com/cases/case12026.htm
He said 'we all should recommend you for a noble prize in your field of study.' after experiencing the powerful Dr. Lin's Natural  Prostaglandin E-1 therapy for prolonging his erection and sexual orgasm, increasing his semen production, darkening his hair, dropping his bad cholesterol level and blood pressure (with a high dose of Yohimbe in DopaFibra!?), eliminating his body pains ...
==> http://www.actionlove.com/cases/case11983.htm
Solution for the post-ejaculation or post-orgasmic brain/nervous disorder, trauma and fatigue - for sexual orgasm
==> http://www.actionlove.com/cases/case11980.htm
She said ' I ordered your products Moodmax, Viagrowth-IV and 5htp for vaginal looseness right before Christmas.... I can say Your products really work. Thank! You have a customer' for Vaginal Tightness and more sexual orgasm! Again, the Dr. Lin's Natural Prostaglandin E-1 Therapy
==>http://www.actionlove.com/cases/case11964.htm
Dr. Lin's Prostatitis solutions - the restoration of sexual orgasm with Natural Prostaglandin E-1 therapy.
==> http://www.actionlove.com/cases/case11924.htm
An endocrinology doctor's experience with over-masturbation or over-ejaculation, resulting in prostatitis, urethritis, erectile dysfunction, low libido, and pains in penis, low back, perineum and anus for no more sexual orgasm -Solution
==> http://www.actionlove.com/cases/case11918.htm
He said ' dear dr lin WOW it worked!!!! i took borage oil 1 capsule a day,3 capsules fish oil and 6 capsules of flaxseed per day.....RESULT- longer sexual intercourse didnt cum as quick and a much harder penis that increased in length by 1 inch and a fatter girth my girl loved my 8inch cannon. i notice also after doing your breathing method i can shoot my big cannon for another round i also take your moodmax and viagrowth4 great stuff' for more sexual orgasm and having Merrier X'mas and happier holidays!
==> http://www.actionlove.com/cases/case11904.htm
He said ' Thank you for a wonderful set of products and information! I have enjoyed them and I believe they have assisted me and my wife to enjoy sex more and conceive a child on our first try!' for a life-term sexual orgasm.
==>http://www.actionlove.com/cases/case11818.htm
He said ' Hello, I have been taking the fish oils and the borage oils now for 4 weeks. I am also very pleased with your products and my hair as well as my wife's hair is turning dark again. My wife has been almost white since her late 30's This is nothing short of a miracle. Thank-you.'  for more sexual orgasm! On Dr. Lin's Natural Prostaglandin E-1 therapeutic formula ==>http://www.actionlove.com/cases/case11805.htm
She has proved what Dr. Lin said - tubaligation results in the state of peri-menopause and menopause transition for PMS and no more sexual orgasm.
==> http://www.actionlove.com/cases/case11800.htm
He said 'Love the products....... my eyesight is so much improved...... I wonder why this is? ' for more sexual orgasm - the electric engineering solution for eyesight and eye floaters.
http://www.actionlove.com/cases/case11735.htm  
He said ' I have been practicing your ballooning method since 1998. I went from 5inches to 7 inches. Then you told me I have probably reached my full potential, that my foreskin was limiting me, which I believe is correct.' on the penile and hair re-growth for more sexual orgasm. On the calculation of the nervous erectile power change based upon the penile shrinkage rate.
http://www.actionlove.com/cases/case11591.htm
How drugs take over your brain and nervous system and how to detoxify your brain and nervous fiber/synapse for restoration of sexual orgasm.
==> http://www.actionlove.com/cases/case11500.htm
When Prostatitis can not be solved by over-ejaculation and antibiotics, you are asking for more troubles - for no more erection (impotency and sexual exhaustion) and sexual orgasm -Solution
==> http://www.actionlove.com/cases/case11430.htm
On seminal retention and prostate-cancer protection, and of course, on Over-masturbation and sexual orgasm
==> http://www.actionlove.com/cases/case11407.htm
He said 'when i take your detox pill i feel really relaxed and think clearly do you know why that is.' a full detoxification of the liver and nervous system for better health and sexual orgasm
==> http://www.actionlove.com/cases/case11347.htm
He said ' By the way, about your 5-htp. ANOTHER GREAT PRODUCT. ... last week when I got the attack, I opened an additional capsule and poured the powder beneath my tongue (sublingually). It COMPLETELY stopped the migraine progressively over a one hour period. WITH NO SIDE EFFECTS!'; more sexual orgasm without headaches and migraine or panic attack.
==> http://www.actionlove.com/cases/case11323.htm
On the role of DHT in the penile Growth, Repair (Re-Growth) and structure for more sexual orgasm.
==> http://www.actionlove.com/cases/case11311.htm
Evidences show destruction of pot (marijuana) smoking, resulting in low libido, erectile dysfunction, premature ejaculation and low seminal production for no more sexual orgasm
==> http://www.actionlove.com/cases/case11303.htm
He said 'first of all, may i thank you for your miracle products, they have totally transformed my life.' ViaPal-hGH-P and 5-HTP have rejuvenated his damaged penis and resumed his seminal production for ejaculation and sexual orgasm through normal vaginal intercourse.
==> http://www.actionlove.com/cases/case11269.htm
He said ' Love+your products= AMAZING! What's going on inside my brain, chemically, since I don't feel like eating? I'm not tired either.'; less foods and more sexual orgasm.
==> http://www.actionlove.com/cases/case11191.htm
He said 'I am nearly at the end of my course of ViaPal-HGH-P (3-010) and I have experienced excellent results. I no longer suffer from extreme fatigue, blurred vision, buzzing ears or nasal congestion after ejaculation. Thank you very much for your help!' on retaining the brain concentration after ejaculating or having sexual orgasm
==> http://www.actionlove.com/cases/case11147.htm
He said 'I feel like a New Man I have No Erection Problems. My erection are very firm and long lasting. I had to take a weaker dosage because I was waking up and walking around with an erection for long periods..' for more sexual orgasm
==> http://www.actionlove.com/cases/case11119.htm
What are the differences between the Penile Ballooning and Penile Exercises/Jelqing/Milking for penile enlargement?
==> http://www.actionlove.com/cases/case11114.htm
On the effect of the vaginal/cervical secretion on penile erection/ballooning and premature ejaculation. Why one tight vagina makes him erect harder and last longer for sexual orgasm , but the other tight one promotes his premature ejaculation?
==> http://www.actionlove.com/cases/case11032.htm
He said 'I could say that you made me a man again.' and gets recovered from extremely sexual exhaustion due to pre-teen over-masturbation; on buzzing ears; Why don’t write a book for parents about how to teach their sons the sexual energy control and development?
==> http://www.actionlove.com/cases/case10924.htm
A MD (a vasectomy victim too!) said 'I had 6 orgasms within a 36 hour period,.... Your products amazingly both help achieve strong erections, reduce the refractory period between intercourses, and maintain sensitivity while enhancing stamina and endurance of erections. Quite unbelievable. ' Oops! excessive sexual orgasm!.
==> http://www.actionlove.com/cases/case10881.htm
She said 'Your products amazed me. After not being very orgasmic at all for 35 years, I began to experience wonderful orgasms often and my libido is sky high. I love it.'  What is the origin of our products?
==> http://www.actionlove.com/cases/case10632.htm
Prostate's seminal production disorder for no more ejaculation and sexual orgasm; Under forcing with a heavy urethral stimulation, the male ejaculation is the same as the female ejaculation fluid.
==> http://www.actionlove.com/cases/case10876.htm
Non-bacterial (non-organic) testicular and penile pains due to ejaculation - why and solution.
==> http://www.actionlove.com/cases/case10853.htm
Neurophysiological approach for overcoming the masturbation addiction
==> http://www.actionlove.com/cases/case10797.htm
Why over-masturbation or excessive clitoral orgasm results in chronic clitoral pains for no more sexual orgasm
==> http://www.actionlove.com/cases/case10793.htm
Viapal-hGH-M has revived a 5-year marijuana smoker's erection for the first times in 5 years! He needs DopaFibra too for a faster healing.
==> http://www.actionlove.com/cases/case10740.htm
Don't let Ecstacy (MDMA) fry your brain and nerves for a short-term fun, but not for a long-term sexual orgasm. Updated - He messed up his brain in 4 months on New Year Eve of 2003!
==>http://www.actionlove.com/cases/case10350.htm
Over-masturbation causes 14-year old boy's endless (continuous) seminal leakage for no sexual orgasm; on destruction of the prostate's ejaculation nervous controller and modulator; The endless ejaculation can cause death during lovemaking, but How to stop it!
==> http://www.actionlove.com/cases/case10592.htm
When 'chronic non-bacterial prostatitis' (now called 'chronic pelvic pain syndrome') is the Prostate's Seminal Blasting Syndrome,' your prostate produces no much semen, resulting in retarded ejaculation, no sexual orgasm and vibrator-induced penile damage..
==> http://www.actionlove.com/cases/case10580.htm
Mechanism of the Penile Ballooning for a better sexual orgasm - on the the 2-stage penile erection theory for Penile Enlargement.
http://www.actionlove.com/cases/case10565.htm
His dog makes his girl friend achieve a Level-7 orgasm,but he gives her intercourse pain for no sexual orgasm. Now, Learn the doggy-style lovemaking.
http://www.actionlove.com/cases/case10535.htm
The final chapter of Penile Enlargement for no sexual orgasm
http://www.actionlove.com/cases/case10492.htm
Dying of Young girl's clitoris and G-spot - losing her sexual orgasm.
==> http://www.actionlove.com/cases/case10292.htm
Excessive sexual orgasm, excessive histamine release, rear-brain and neck pain, orgasmic nasal congestion, allergic responses, and dark eye circles.
==> http://www.actionlove.com/cases/case10263.htm
Cause and Solution of orgasmic convulsions upon ejaculating - the seizure response to sexual orgasm
==> http://www.actionlove.com/cases/case10241.htm
He said ' You "My Friend" are the King of Love'; ViaPal-hGH-M resolves his Chronic penile pain; On Dr. Lin's Bioelectric Theory of Love Science.
==> http://www.actionlove.com/cases/case10097.htm
On the Liver P450 Detoxification and the liver protection for health and sexual orgasm
==> http://www.actionlove.com/cases/case10000.htm

General Solutions for women without experiencing sexual orgasm
==> http://www.actionlove.com/cases/case9864.htm
But, what are General causes? Here are the General problems:

How to enlarge (loosen)  your vagina, shrink (yes, kill ) your clitoris and G-spot, and produce urinary/bowel incontinence? (click here for destruction of vibrator); How to become an impotent young man? (click here); How to shrink your penis?(click here) or How to break a penis! (click here with women-wild rides or penile enlargement practices); How to destroy (castrate) your sexual functions by masturbation, drugs (including SSRIs and birth control pills/shot - one shot kills it all!), or Vasectomy( - two cuts kill them all;) How to get a pseudo-prostatitis; How to produce eye floaters;  Finally, you want to know how to become a fastest semen-shooting (ejaculation)  man in lovemaking or dry up your seminal ejaculation or production.  
The variation of the brain's neurotransmitters in response to ejaculation and sexual orgasm - on the Penile Ballooning Method for penile enlargement and the destruction by over-masturbation and over-ejaculation .
==> http://www.actionlove.com/cases/case9875.htm
Destruction produced by Male or Female Over-Masturbation for no sexual orgasm.
==> http://www.actionlove.com/cases/case9848.htm
The principles of the Penile/G-spot/Clitoral enlargement and
Vaginal Narrowing (Reduction, yes!) are the same thing! for more sexual orgasm.
==> http://www.actionlove.com/cases/case9819.htm
Brain's and nervous functions, Orgasm Headache, and nausea associated with excessive sexual orgasm (Orgasmic Stress); on anorgasm, stress effects and de-stress.
==> http://www.actionlove.com/cases/case9814.htm
When the holes down there become bigger, they will cause pain, but why? So, How to downsize the holes for men and women. Yes, his and hers!
==> http://www.actionlove.com/cases/case9767.htm
Causes and solutions for PMS, Intercourse, penetration or orgasm pains/cramps, tilted or prolapsed uterus, and sexual orgasm; Love Positions and vaginal air trapping/pumping/escaping.
==> http://www.actionlove.com/cases/case9756.htm 
He said ' I want you to KNOW that your 'pills' have done more for me..' beyond sexual orgasm.
==>http://www.actionlove.com/cases/case9689.htm
Penile Enlargement, DHT, Prostaglandins, Nitric Oxide and cGMP
==> http://www.actionlove.com/cases/case9663.htm
On Penile Enlargement and  Reader's experience on Dr. Lin's Male Multiple Orgasms without ejaculation.
==> http://www.actionlove.com/cases/case9647.htm
Mechanism of sexual orgasm, damage of sexual nerves, and lesson from labor orgasm
==> http://www.actionlove.com/cases/case9589.htm
How do you know she achieve orgasm? on Penile Size and Penile enlargement, female sexual orgasm responses and dysfunction.
http://www.actionlove.com/cases/case9566.htm
Hair loss, 5-alpha reductase, prostate enlargement, erectile dysfunction, Prostaglandin, Vaginismus, Intercourse pain, Oxytocin and powerful sexual orgasm
==> http://www.actionlove.com/cases/case9580.htm
Principles and mechanisms of the Natural Penile Enlargement - Ballooning Method for more erection and sexual orgasm
==> http://www.actionlove.com/cases/case9499.htm
How to become a multiple Sexual-Orgasms couple.
==> http://www.actionlove.com/cases/case9303.htm
Male multiple orgasms without ejaculation by the Anal Breathing Method - The principle, tricks and conditions.
==>http://www.actionlove.com/cases/case9422.htm

Do you want to know More Good News for Sexual Orgasm? Click Here; Or the most self-destructive Sexual Practice (click here)?

Interaction between the brain/nervous systems and the love-power generators (uterus, cervix and ovaries); no hysterectomy if avoidable.
==> http://www.actionlove.com/cases/case9341.htm 
She said 'following your advice my husband has a new penis' and 'I had 30% less flow - relief' from heavy menstruation with your CD-ROM and products. For better sexual orgasm
==> http://www.actionlove.com/cases/case9275.htm
She said 'I orgasmed 3 times! AND, my husband had his first multiple orgasm.' with Dr.Lin's Sexual ChiKong Intercourse technique
==>http://www.actionlove.com/cases/case9171.htm
Neurophysiological Explanation of Sexual ChiKong Intercourse for multiple sexual orgasms and ejaculation control
==>http://www.actionlove.com/cases/case9194.htm
She has enlarged her Clitoris and G-spot with ViaGrowth-IV and Finger Pliers and Penile Screwing massages for more intensive sexual orgasm; but how to continue the practice without him.
==>http://www.actionlove.com/cases/case9214.htm
Over-masturbation and over-ejaculation result in impotency, premature ejaculation, headache, memory loss, yellowish face, and absentmindedness - the Solution.
==>