I already received very interesting information about the problems that I have with my pois, you can find explanation and treatment for my case but I think that it will be very similar for many pois suffers. see the information below for details.
Thanks.
Hello,
Experiencing the symptoms listed is usually indicative of a moderate to severe case of sexual exhaustion, largely depending on a set of factors and the actual severity of the symptoms.
Somewhere along the road of exhaustion one usually develops a negative self supporting neuroplasticity, which is a term I use to describe inabilities of an organism to restore itself to a proper state (by what is considered to be the once positive functioning) and neuroplasticity through its own neurohormones, hormones, and neurotransmitters that are needed to recharge it in the first place.
Tests are usually ineffective in detecting the imbalanced state through the inability to monitor neurotransmitter levels in the brain, the wide range of acceptable results, and the flat ratio of hormone-neurohormone-neurotransmitter interactions monitored.
Every symptom and the underlined causes for the symptoms experienced is just a direct result of an ongoing process which involves mainly nervous and endocrine systems.
One can exhaust and/or ruin his internal organism balance through numerous activities - usually ill lifestyle and mental burdens, as well as the sexual activities strain on the endocrine and nervous system. We also shouldn't neglect and generall predisposition for exhaustion through certain receptor gene mutations. For instance, around 20% of the patients treated for sexual exhaustion tend to have experienced minor and rare aura migraine attacks at young age, long before the actual exhaustion took place. However, given the right circumstances, anyone can eventually exhaust his organism, reach the "breaking point" and basically stuck in a cycle of inflammation.
It's a self supporting exhaustion through:
-Lowered or/and severely imbalanced levels of acetylcholine, serotonin, dopamine, and GABA levels which usually leads to deranged organism functioning and a wide set of symptoms. However, the most notable consequence of this imbalance is arguably the chronically heightened stress response through inadequate serotonin-GABA modulation on neuronal activity. As a direct result, excessive cortisol and prostaglandin E2 in tissues and brain - once important for proper organism behavioral modulation and adaptation through times of acute stressor exposure, will create the negative neuroplasticity even faster. It would be somewhat of a simplification to blame every symptom on imbalances in just the levels of these neurottransmitters, but they are to serve as a straightforward indicator and eventual major and influential link of stability in proper organism functioning.
-Adrenal gland adjustments to chronically create more stress and inflammatory hormones, such as cortisol and epinephrine at the expense of DHEA
-Artery constriction for less blood flow and thus increased local inflammation
-The increased levels of cortisol, prostaglandin E2, norepinephrine, epinephrine, and especially prolactin will negatively affect the levels of GnRH, LH and FSH, and together with the arterial inflammation and constriction may kill testicular function as well as hypothalamic-pituitary-adrenal-testicular axis' proper functioning. Less androgens to modulate inflammatory response, testicular tissue health, insulin resistence, energy levels, tissue and testicular health, proper nts. and hormonal conversions, and neurotransmitters homeostasis will result in even more vicious cycle of inflammation to suppress them even further through low dopamine levels and chronically heightened prolactin. The overactive sexual activities will slowly drain the organism of its potential for rejuvenation.
You can see how this state may manifest in a wide range of symptoms through individual gene expressions. However, the symptoms you've listed can be mainly contributed to improper serotonin-dopamine-acetylcholine-GABA ratio/levels for weakened nervous modulation on excitatory and inflammatory response and abnormal hypothalamic-pituitary-adrenal-testicular axis functioning for lowered androgens levels.
If there's anything positive it is that you probably haven't injured your penis or experiencing any severe abnormalities in its shape. It is usually in this condition when most injuries happen. Even forceful masturbation may result in excessive inflammatory response and collagen scar tissue release, not to mention jelqing or stretching.
Usually the way to go is to transform your neuroplasticity to a positive one. The inter neuronal connections have been developed and ordered to process information in a specific manner. You may experience severe difficulties in rewriting their work to induce proper (by what you consider a proper response) responses in certain situations.
The first step is to create what you would consider a positive neuroplasticity and keep it for a prolonged period of time.
Every problem must be addressed simultaneously to avoid feedback reactions supporting the developed negative neuroplasticity. That's why just a random set of products or supplements of any kind will prove to be ineffective.
For starters there are some things you may consider doing, such as exercise - running is very beneficial especially for NO and hGH boosts, proper diet (much fiber, fruits, avoid milk with prostaglandin E2 analogs, avoid much red meat, no soy or refined sugar either), negative ion exposure, and massages.
Discontinue sexual activities for 2 to 4 weeks and then limit masturbation as well as other similar in nature activities to 3-5 times a week for 3 to 5 months.
Alpha-Amino, Multi-Alpha, Griffonia simplicifolia - 5HTP (half the dosage, should gradually discontinue it 2nd to 3rd month), GRB6-GABA (should gradually discontinue it 2nd to 3rd month), Alpha-HGH and Ultra-Purified-FishOil for the specific case, will improve nervous and endocrine functioning, stabilize acetylcholine, serotonin, dopamine, GABA levels, aid hypothalamic-pituitary-adrenal-testicular axis proper functioning, restore proper serotonin-GABA nervous modulation on excitatory and inflammatory response, increase androgens, increase elasticity prostaglandin E1 E3 and Nitric Oxide, alter numerous gene expressions, and eventually rewrite the negative neuroplasticity developed.
Note that the primary goal for the first 2 to 3 months is to restore the proper acetylcholine-dopamine-serotonin-GABA levels and ratio and modulation on inflammatory response (as well as proper dopamine-norepinephrine-epinephrine conversions and dopamine-prolactin ratio). You would then need to monitor your overall stress levels (both physical and mental) for some months to make sure you're keeping the neuroplasticity that has been developed.
Please, keep me updated on the case.
Glad if I could help!
Best Regards,
dr.Richards, MD
