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Case Title: Vasectomy interferes the vagus and L1/L2 nervous function samong the testicular(epididymis), liver, pancreas and adrenal medulla for no sexual orgasm
Reader: 7/17/2005>
Can you explain how a vasectomy kills testosterone production in laymen terms... maybe use an analogy or detail the mechanics in a more simple fashion? I tried to follow your explanation below pasted from your website.
Here are some of my questions which when answered may help clarify your explanation below"
1) how does pressure increase in epididymis affect brain metabolic functions dramatically?
2) what is modulation change mean? ... in L1/L2 and vagal outflow.
3) what does innervate the white tissue of the epididymis mean? how is this adverse?
------------------------------------------------------------------------------------------
<snip from actionlove.com>
"After vasectomy, the sperm pressure inside the epididymis will alternate (interfere or suppress) the brain metabolic functions, and sexual responses through the modulation change in sympathetic (L1/L2) and vagal outflow, where the sympathetic nerves innervate the white adipose tissue of the epididymis, inter scapular brown adipose tissue, pancreas, liver and adrenal medulla, and the vagus nerve innervate the pancreas and liver. "

Dr. Lin: 7/18/2005>Yes.
1. There are a vagus and sympathetic L1/L2 nervous sensory circuits in the testicles and particularly epididymis. The vagus circuit is responsible to feed back to the hypothalamus-pituitary function for release the FSH, LH, prolactin and oxytocin to control the testicular function. The L1/L2 nerves are responsible to jumping up the testicular function for sexual excitation and the sperms release during the orgasmic contraction.
2. Modulation means that the nervous systems adjusts the amount of the FSH, LH, prolactin and oxytocin release to control or stimulate the testicular function.
3. The sympathetic L1/L2 nerves from the spinal cord discs L1 and L2 interconnects the white adipose tissue (WAT) of epididymis, inter scapular brown adipose tissue (BAT), pancreas, liver, and adrenal medulla, and the vagus nerves interconnects the pancreas and liver with the WAT of the epididymis. The L1/L2 connection tells that sexual arousal and orgasm will change the testicular function, pancreas, liver and adrenal medulla function in supporting the DHT, androstenedione, testosterone and DHT production and burning in support sex acts and the dopamine/norepeinephrine to epinephrine conversion for the prostaglandin E-2 synthesis (for tension pain and ejaculation), orgasm/ejaculation contraction or erectione withdrawal. The L1/L2 nervous action for contraction is to expel the sperms out of the epididymis with prostaglandins E-1 and E-2 where Prostaglandin E-1 is to protect sperms and Prostaglandin E-2 to kill the natrual antibiotics and to suppress the immunity in the vagina or anus/rectum (anal sex) or any parts of the contact area for sperms to survive. The vagus nervous function is to promote the hGH, DHEA, androstenedione, testosterone, DHT and prostaglandin E-1 synthesis for body restoration and healing when the body is at rest. Vasectomy usually forces sperms to accumulate and build a pressure against the epididymis and testicles, and therefore induces a mass production of prostaglandin E-2 for pains and immune disorders where sperms are piled up together.

Reader: 7/19/2005>
Dr. Lin... the clarification was very helpful... thank you!
Obviously, urologist who perform many vasectomies a year don't believe there is any such negative outcome and work hard to keep you from thinking so. If you talk to Drs. who specialize in reversal... you will find that they recognize that rupture or obstruction of the epididymal tubule (caused by increased pressure in the vas deferens and epididymis below the level of the vasectomy site) can increase procedure complexity and reduce overall reversal success, i.e. less chance of healthy sperm renewal for pregnancy. And... that the more time that has pasted from the vasectomy, the greater the chances of this problem occuring.
Why don't these Drs. go one more step and admit the vasectomy is causing the problems?!?
In fact... I may see if I can't stealthfully challenge a few Drs. who specialize in reversal to see if I can get them to state this outrightly.
In the meantime... if it has been 6 years since my procedure, do you think there is a good chance that a reversal could solve many of my problems: low testosterone, depression, thyroiditis? If so, the reversal costs could very well be less than all the RX I am having to take and will continue to add up over the years.
Dr. Lin: 7/19/2005>
So, the vasectomy-reversal doctors know the side effects of vasectomy on the testicle health!
Well, with the contract agreement, The vasectomy urologists can get away from the problems created by the surgery since the vasectomy operation has never touched your testicles at all. It is a cellular biological response to vasectomy causing the problem, not a well-defined medical malpractice. The induced nervous disorders can be not detected /measured by any high-tech medical instruments either, so that the medical society can continue enjoying the legal malpractice upon your request.
Since you are still young, age 34, vasectomy reversal and NO/oxytocinergic excitation on the testicles with promting prostaglandin E-1 synthesis can help you gradually improve your conditions, as given in
Vasectomy reversal releases his testicular pains; restore the hypothalamus-pituitary-axis with ViaPal-hGH-P for sexual orgasm again.
==> http://www.actionlove.com/cases/case13019.htm 
A vasectomy victim said ' I have been taking the products you suggested and they are helping. I had my vasectomy reversed (Jan. 2005)and the pain is almost completely gone now. I am once again waking up with erections and premature ejaculation is gone ejaculation volume is getting larger. ....I noticed premature ejaculation stopped as soon as I started using your products and I have never understood how the vasectomy caused this problem but I do know the reversal and your products have done wonders to help restore my sexual health.' no more pain and no more premature ejaculation - for restoration of the vasectomy-damaged testicular and sexual orgasm
==> http://www.actionlove.com/cases/case13536.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 
A vasectomized customer said' I ordered your viapalhghp and after taking the maximum dosage i finally saw an improvement in my sex drive....,My total t level was 681ng/dl ' for better ejaculation control and sexual orgasm; On increasing sperm production after a vasectomy reversal for baby making.
==> http://www.actionlove.com/cases/case11206.htm 
Viapal-hGH-P has started to reactivate his spematogenic cells for sperm production after his reversal vasectomy for sexual orgasm.
==> http://www.actionlove.com/cases/case10136.htm 
He said 'The product really seems to help since I have had a vasectomy' for erection, semen production and sexual orgasm.
==>http://www.actionlove.com/cases/case10087.htm 
He said 'I have received ViaPal-hGH-M and notice improvement already!' within a week for Vasectomy men to erect harder and ejaculate more and thicker.
==>http://www.actionlove.com/cases/case10036.htm 

Here are the articls you may be interested -
1: Vagotomy suppresses cephalic phase insulin release in sheep.
 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=
Abstract&list_uids=10362854&query_hl=1  
2:  Reflex effects from leptin sensors in the white adipose tissue of the epididymis to the efferent activity of the sympathetic and vagus nerve in the rat.
 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=
Abstract&list_uids=10203247&query_hl=9    
3: Central nervous system origins of the sympathetic nervous system outflow to white adipose tissue.  http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=
pubmed&dopt=Abstract&list_uids=9688991&query_hl=9 

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