Atributos de directorio PKI

Example #2 A

The use of multiple esters can create timing problems. In Frank's case this was simply solved, at times, by inducing a continuous daily plasma level of a chosen threshold, then continued with the same level during the high androgenic to high anabolic transition.

The example as shown induced a daily plasma level of about 250mg daily until day #24. At that point the plasma level gradually ramped-down (tapered off) until about day #36. However, it should be noted that by day #30 the existing plasma level were not excessive and therefore allowed Frank to stay within our intended 30 day high- activity time frame.

This was about a 33% Androgenic Dominance Period, 33% Androgenic/Anabolic Equivocal Period, And 33% Anabolic Dominance Period example. Some advanced athletes have cut the listed dosages in half and still made excellent progress. This was easily done by either utilizing the every-other-day listed dosages, or by cutting the dosage schedule in half. It should seem obvious that intermediate level athletes of my creation further decreased the dosage schedule to stay within acceptable ranges.

The example as listed was a single-ramp protocol that came on pretty fast due to Sustanon-250 containing 2 fast acting esters (Testosterone Propionate and Phenylpropionate). The use of Durabolin during the Anabolic Dominance Period was utilized to replace the declining plasma level of Testosterone Propionate contained in Sustanon-250. In truth this was not necessary, but it shows how a protocol was made far more efficient than was normally applied. This addition did increase the anabolic edge to some degree.

When Frank chose to induce an even quicker androgenic ramp he added an oral AAS up-front: Dianabol 40 mg/d on day #1-3, 30 mg/d on day #4-6, and 20mg/d on day #7-9. Since Dianabol is highly anti-catabolic in nature this addition helped to hold off the body's initial cortisol reaction a bit longer when administered for this brief period.

Example #2 B

By mixing testosterone Propionate, Testosterone Enanthate, and Testosterone Cypionate, the androgenic period up-ramp came on pretty fast. This closely simulated Sustanon 250 in action and effects. The use of Durabolin, Equipoise, and Deca Durabolin mimicked the active and half-lives of the Testosterones as listed in order.

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1. Durabolin/Testosterone Propionate -72 hour active-life, 36 hour half-life. 2. Equipoise/Testosterone Enanthate -8 day active-life, 4 day half-life.

4. Deca Durabolin /testosterone Cypionate 14-16 day active-life, 7-8 day half-life.

* Interesting: I have found 2 active and half-life listings for Equipoise (Boldenone Undecylenate) 16 and 8 days as well as 8 and 4 days respectively.

Monitoring blood tests however supports the latter more closely.

This example also established about a 250 MG daily plasma level and had nearly the same androgenic/anabolic dominance ratio. Since any example shown that provided a 250 MG daily plasma level was an upper effective threshold, this too was a very advanced protocol. All advanced athletes such as Frank made exceptional progress by utilizing the injection dates and dosages listed on odd days only (which allowed for a 125 MG/D plasma level).

As in example #2 A, novice and intermediate Testosterone users followed the odd day only (EOD) protocol and cut dosages in half (this provided a 62.5 MG/D plasma level). This example provided excellent results as discussed. But the effects were compounded when administered as a Max Mix and site injection protocol (Which we will discuss later). This was a single ramp example.

Again, sometimes getting creative with esters was just fun. And it was a chance to clean out the gear-box from unused post-cycle chemistry. Of course, this example has been simplified by utilizing one Testosterone ester with one high anabolic ester and adding an androgenic oral in the front... when needed.

Example #2 C

Example #2 C utilized all short /fast acting esters. Each of which had an active -

life of about 72 hours and a half-life of 36 hours.

For athletes that were prone to estrogenic side effects I liked Masteron up-front in some Max Androgen Phases for 2 reasons:

1. It is more androgenic than Testosterone.

2. It possessed strong anti-estrogen qualities. Add to this its anti-catabolic effect and quick up-ramping effect.

The use of Testosterone Propionate in a Max Androgen Phase had advantages:

1. Time frames were easily controlled. It ramped up IGF-1 production in the liver. 2. It was a more singular potent Testosterone than any other except Suspension.

The use of Durabolin was perfect for well-timed high androgenic to high anabolic period transition. However, since it was only moderate-low androgenically, it was best utilized by those who had above average post-cycle lean mass loss problems.

If the reader has been doing the Math on active and half-lives, you already know this was another very advanced dosage threshold of 250 MG/D and how it was adjusted for advanced, Intermediate, and Novice threshold levels. Learn the Math! It took the guess work out of any protocol.

The reader should also realize this was a single ramp example and that the most effective period was from about day #3 to about day #2 7. Would orals have been effective up front? No! But you knew that already. Right?

* Now, can you do the Math for most effective periods for example #2 A, and B? By using a graph anyone can.

We have the first two phases down ... let's move on to next page and take a look at phase three ...

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MAX ANDROGEN PHASE