SECCIÓN 3 – MARCO DE CERTIFICADOS DE ATRIBUTO
15.1 Extensiones de gestión básica de privilegios
Fareston (toremifene citrate) is an estrogen receptor mixed agonist/antagonist.
In fact it is classified as a true Selective Estrogen Receptor Modulator. This means that the drug is selective in specific types of estrogen receptors it blocks and those it activates. For AAS users this is a real plus due to the reality that many estrogen receptor antagonists hinder glucose storage and GH release...and Fareston does not.
Sadly, it use also hinders LH/FSH production thus having no value in HPTA regeneration. In studies upon males there was a marked reduction in HPTA activity resulting in a decrease in androgen and sperm production. But on a plus side it has a positive effect upon cholesterol levels favoring HDL (good cholesterol) production and significant LDL (bad cholesterol) reduction.
An effective daily dosage for Fareston is 60mg/d and it best administered as such even with its half-life of over 4 days. This is like Clomid in that the daily accumulation acts as a buffer for physiological adaptation to some extent.
*l note this only due to a bottle I came across that had the right name but the wrong chemical on the label.
FARESTON (toremifene citrate) Tablets for oral administration each contain 88.5 mg of toremifene citrate, which is equivalent to 60 mg toremifene. FARESTON is a nonsteroidal antiestrogen. The chemical name of toremifene is: 2-(p-[(Z)-4-chloro-l ,2- diphenyl-1 -butenyl]-phenoxy)-N,N-dimethylethylamine citrate (1:1).
B a c k T o B r e a s t I m p l a n t s . . . E r r . . . I M e a n , S i t e I n j e c t i o n s . . .
The idea of site-injection protocols was similar to the intent of breast implants. Only in this case, the muscular tissue size was real. Let me explain.
Muscle is like water in a fish tank. Muscle is the water, and the fascia that encases and contains it is the tank. If the fascia is stretched and enlarged, muscular tissue will, in time, fill the larger area. When inert (Hopefully) substances such as Synthol were injected directly into a muscle belly in great enough volume (In an
accumulative manner) the fascia containing muscle fibers and the fascia containing
the individual muscle section itself had to stretch in order to maintain a sort of balance or homeostasis.
When a product such as those offered by Hardcore Muscle Gear (hmgear.com), that contained free prosteroids and prohormones (which were free non-esterized androgens) was utilized, the hypertrophy of muscle cells accelerated thus filling the new area with vascular tissue more quickly. And when an AAS mixture was utilized with the SEO, growth was increased again.
Almost any cycle structure one could think of has been utilized as a site- injection protocol. However, some were significantly more effective than others. Personally, I preferred faster acting esters or non-esters because cycles were easier to control for length of activity and the maintenance injection periods did not interfere with probable release periods of long acting AAS. More important the AAS activity was readily available site-specifically for symmetry alterations.
WHAT IS AN ESTER AND WHY WOULD ANYONE CARE?
First let me explain, esters and long-vs-fast acting AAS. Way back when testosterone was first isolated and utilized as an injected exogenous steroid, raw testosterone (Like suspension) was the only choice. Raw testosterone is not very soluble. It dissolves better in water or blood than in fats, but not much better.
As you know, fats take a longer period to be metabolized and some fats take longer than others. So chemists decided to make testosterone fat soluble, which involves the additions of an ester to the AAS molecule.
The ester causes the AAS to remain within fat contained in muscular tissue until an enzyme called esterase helps it to get into the blood stream by cleaving the ester chain and freeing the attached AAS. This created a time-release effect. Cool, huh? As said prior, different esters have different release rates. This is how half and active- lives of many injection type drugs including AAS are created.
This is how half and active-lives of AAS are created, okay?
The Synthol and Hardcore Muscle Gear products Frank used were sterile (Again: so they claimed and I have tested both products. Yes, "the batches" I tested were clean) fatty acids. Remember that part. Fatty acids in these products had to be cleaved by the ester enzymes. So they too remained in muscular tissue for a period.
Once cleaved, they entered the blood stream and were likely metabolized as food. So site-injection Max Mixes were mostly created utilizing faster acting esters and non-ester products corresponding more closely with the period it took esterase to act upon the Protest or other space occupier.
It was not necessary, only preferable for control of periods utilizing AAS so as to avoid as many counter measures to growth as possible. Action/reaction, remember?
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Maintenance periods had to be about 6 months for more permanent size increases and could over lap or be part of repeat cycles and phases we constructed. *lt is important to remember that site enhancement techniques provide actual increased growth best for those who have increased their muscle mass to a point where fascia is constricting growth prior to employment. Joe Blow newbee to training realized the least benefits.
Editor's Note: Please allow me to further clarify the above. Site injections work ...
you inject, that muscle will look and feel bigger and better. Pumps will even be better. So far, so good ...
But you will realize the MOST and BEST effects when you are more of an advanced bodybuilder who has pretty much done everything they can think of to make that specific muscle grow and nothing works any more. At that point, the "fascia " is so darn HARD, that it's just not going to give any more room to growth and hence, your muscles just have to sit there and stay the same size.
Now THIS is when site enhancement techniques work best. When you inject this oil continuously, the fascia has no choice but to expand and stretch out. Do this long enough with enough oil and it will stretch out and STAY stretched and BAM, now you have more free space that needs to be filled up with muscle.
So, now your muscle can BREATHE again and grow some more. It may not be much. Half an inch to as much as 2 inches for some lucky individuals. But hey, I'll take even a centimeter these days.
Almost any muscle imagined has been localized for site-injection protocols, but some were more difficult than others. Smaller muscles with shorter length and distinct bellies were easiest. Biceps, triceps, anterior and posterior or lateral delts, and calves for example. However Frank's pecs, lats and even traps were successfully localized.
Personally I believe the best permanent and natural results for any one area localized were best accomplished during a 6-month period and then discontinuance for 3-6 months. The reason was simple. It took time for vascular tissue to effectively fill the new area. When the site-injection space occupier was discontinued the oils were allowed to migrate out and the natural hardness returned to the muscle.
*Anyone who watched the top 5-bodybuilding competitors in recent years had to have noticed things like very hard, tight, and dry competitors who had these balloon like delts and biceps with almost no definition (As well as other body parts). The rest of the musculature looked like rock while the over extended site-injection localized
muscles just looked like bags of oil. This was due to athletes using large volume site- injection protocols too close to competition.
"Bigger is not better if it looks stupid and fake. Using arms for an example, it is possible to add 2-3" in size within a few weeks, my lad, but it looks very soft and lumpy."
While maintenance periods were utilized and other phases were completed, vascular tissue filled the new areas. The total size gain during the 6-month period was at times more than 2-3", but once discontinued and the space occupier migrated out, it was about 1-2" of new muscle area (from the initial protocol) that remained in most cases. Even in the best chemistry environments the tissue can only grow so fast. But when was the last time a veteran bodybuilder put 1 -2" on his arms in under a year?
When not enough size was accomplished, it was simple to do it all again 3-6 months later. Since Frank did not compete again for about 2 years, the time allowed for 3 sets of sites to be localized and a 6-month clean-out period before competition. His arms were well over 21" first time back in the lights and his shoulders noted to be atleast 2" wider with much fuller pecs and lats...and deep cuts in all.
During the initial fascia stretching period of 3-4 weeks, 2-5 ml of Max Mix was utilized per site. Biceps for example was 2-5 ml injected 2-4 times weekly using 2-5 ml in each outer head. Then a maintenance period of 5-6 months consisting of one 2- 5 ml weekly injection in each bicep was followed.
Since Frank's arms were his size/symmetry weak point, his first Max Mix needed to allow enough mixture volume to accommodate the number of sites while maintaining a pre-determined plasma threshold level. When the area being localized was larger, such as lats, the volume or amount of Max Mix needed to be greater but with the same total AAS mg as intended for the total daily plasma threshold. (More on that later) For now, I will put it this way. When each bicep was to receive 3 ml and the total AAS dosage intended was 100 mg, then the larger volume (say 10 ml divided into multiple administrations) for each lat was adjusted to also contain a total of 100 mg of AAS.
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THE CRITERIA UTILIZED FOR CREATING A MAX MIX:
The best stacks consisted of a good testosterone, a high androgenic, and an AAS that remains anabolic in a catabolic environment.
"A little Methandriol Dipropionate helped make receptors more sensitive.) TESTOSTERONES Decanoate-Propionate-Undecanoate -Phenylpropionate-Enanthate Suspension HIGH ANDROGENS Parabolan-Finajet (Trenbolones) DHT-Finabolan-Masteron ANABOLICS
Nandrolones (Esterless-Phenylpropionate-Decanoate-Cypionate in a pinch) Primobolan Depot-Masteron-Equipoise-Winstrol Depot (Masteron is a high androgen but has great anti-catabolic qualities and does not aromatize)
I have always liked the localized anti-catabolic effect of esterless nandrolone for site- specific enhancement.
Note: The best results came from esterless, acetate and propionate AAS in that order.