Estrogen Control NOT Elimination

Estrogen control was paramount for health and long-term result potential. But estrogen can increase IGF-1 production too, which was good. Estrogen also increases androgen receptor-site sensitivity. So we wanted estrogen to run rampid for the first two weeks of Frank's Max Androgen Phases without allowing it to cause gyno and female pattern fat deposits. Simple: We used an estrogen antagonist to block receptor-sites but allowed plasma estrogen levels to remain high.

Using Clomid as an example, it has been my experience that a novice AAS user required (if any) only 50 mg/d (50 mg per day). And an intermediate AAS user required 20-30 mg/d. An advanced AAS user commonly required 30-50 mg/d. A very advanced AAS user sometimes required 40-60 mg/d, and in most cases, some additional help from an aromatase inhibitor.

The key was to watch for signs of gyno and female pattern fat deposits, while keeping a close eye on blood pressure. This was always of the utmost concern during the building of the perfect beast. High blood pressure can introduce a variety of long term and life threatening negative side effects.

"Nolvadex decreases GH/IGF-1 synthesis and is therefore a poor choice as an estrogen antagonist.

Things we have learned from experience...

Estrogen levels were kept near normal or below before we exited the AAS protocols. So we added an estrogen esterase inhibitor at about day #15 of a Max Androgen Phase to clear the system of excess estrogen before we exited. I have not noted many novice AAS/Max Androgen Phase users whom needed this precaution. But this was in relevance to dosages administered.

Some intermediate AAS users opted for Arimidex 0.5-1.0 mg/d, or Proviron 50100 mg/d. Most advanced AAS users successfully utilized Arimidex 1.0-2.0 mg/d or Aromasin 50mg/d. This was, of course, unnecessary when a Cortisol/Estrogen Suppression Phase was layered in at the half-way point or beginning day #15 of a Max Androgen Phase.

"Patience, Grasshopper""

Coctciv

I have and will repeat this fact again and again: Any effective plasma threshold exceeded before it failed to provide results was a growth period lost. This was true of any chemical muscle enhancer. This is in fact why so many athletes reached only 5070 % of their potential. Receptor-site insensitivity (not AAS receptor sites) and the body learning new tricks to force homeostasis was the number one reason why we had often seen 220 LB 6 foot off-season bodybuilders using crazy dosages with poor results.

Of course there are ways to beat this too that I created for Frank, but we will discuss that later. First let's look at what the basic threshold for results were when long term potential and permanent gains were to be realized.

Since this section is about Frank's AAS protocols, let's focus upon them for now. Growth thresholds were established by plasma level in this discussion. Although there were several thresholds for each level of experience and drug, there were predictable ranges of dosages expressed in daily plasma levels we used as a basis.

First let me say again that it has been my experience that no athlete should have ever utilize AAS or other muscle chemistry until they have trained hard-core for at least 2-3 years as a natural.

If this was Frank, and he was a natural or somewhere in between, I would have utilized the following rough guide-lines. Natural training is a growth threshold also. I have trained some 250 LB, 8% body fat naturals, too.

"Never waste a growth threshold. You need to do the physical work required first and foremost, you weenie""

MAX ANDROGEN PHASE DOSAGES (EXAMPLES) (Actual Dosage of Androgen Minus Ester Weight)

Novice

Intermediate

Advanced

Very Advanced

1.0-2.0 mg/lb weekly

2.0-3.5 mg/lb weekly

3.5-6.75 mg/lb weekly

6.75-insanity mg/lb weekly

31.25-62.5 mg/d plasma level

62.5-125 mg/d plasma level

125-250 mg/d plasma level

250 mg/d plasma level

218 mg-437.5 mg total weekly

437.5 mg-875 mg total weekly

875 mg-1750 mg total weekly

Above 1750 mg total weekly

As I said, these are the rough guide-lines I utilized and they assumed bodyweights of the following with below 12% bodyfat:

Novices: 1 85-218 LBS Intermediates: 218 240 LBS Advanced: 240-265 LBS Very Advanced: 265 and up.

Of course bone structure and height played a role in potential weight/mass possibilities as did genetics. However, I have met few "average" individuals who could not have realized at least 265 LBS-plus with an off-season body fat level below 12%. Those who have failed usually did so by not planning for long-term potential adequately.

"By learning Phase Cycling and Action/Reaction Factors this, like most obstacles, can be over come."

Now that I have established some of the criteria utilized and incorporated into structuring protocols employed by Frank N. Steroid, it is time to discuss how it was applied.

The examples that follow are not intended as a guide or endorsement. They are simply what they are: The synergistic protocols that were used to build the perfect beasts, and another piece of Frank's story.

DAY

A.

B.

C.

1.

Theramex 250 mg

Theramex 500 mg

Theramex 250 mg

2.

Theramex 250 mg

Theramex 500 mg

Theramex 250 mg

3.

Theramex 250 mg

Theramex 500 mg

Theramex 250 mg

4.

Theramex 250 mg

Theramex 500 mg

Theramex 250 mg

5.

Theramex 250 mg

Theramex 500 mg

Theramex 250 mg

6.

Theramex 250 mg

Theramex 250 mg

7.

Theramex 250 mg

Theramex 250 mg

8.

Theramex 250 mg

Theramex 250 mg

9.

Theramex 250 mg

Theramex 250 mg

10.

Theramex 250 mg

Theramex 250 mg

11.

Deca 200 m g

12.

Deca 200 mg

13.

Deca 200 m g

14.

Deca 200 mg

15.

Deca 400 mg

Deca 200 m g

16.

Deca 400 m g

Deca 200 m g

17.

Deca 400 mg

Deca 200 mg

18.

Deca 400 m g

Deca 200 mg

19.

Deca 400 mg

Deca 200 mg

20.

Durabolin 25 mg

Deca 200 mg

21.

22.

Durabolin 50 mg

23.

24.

Durabolin 75 mg

25.

26.

Durabolin 100 mg

27.

28.

Durabolin 125 mg

Deca = Deca Durabolan (nandrolone decanoate)

Deca = Deca Durabolan (nandrolone decanoate)

Example #1 A

Theramex is a long acting testosterone. Like all testosterones it is highly androgenic and highly anabolic. It seems to be a common error to list the drug as a more powerful testosterone. Since this drug is esterized, suspension is still the more active. Theramex has an active-life of about 20 days and a half-life of about 10 days. Theramex in this example remained active in down-ramping dosages until day #30.

Durabolin is a short or fast acting nandrolone that is highly anabolic and moderate - low androgenic. It is also very protein sparing like all nandrolones. Durabolin has an active-life of about 3 days and a half-life of about 1.5 days. Durabolin will remain effectively active in this example until day #30-31.

Example #1 A was a single ramp Max Androgen Phase that was the first of the AAS protocols structured for my beast. This means that the plasma level established by Theramex was maintained and then replaced by Durabolin as Theramex daily plasma levels ramped down. This allowed for an excellent transition from a high androgen to a high anabolic environment.

If you look at the rough graph you will see this cycle example had a potential 20-day "most effective period" from about day #10-30. This is not to say that the first 10 days lacked activity of course. Naturally to waste any portion of a phase without gaining maximum results before the body could mount counter measures to alterations in homeostasis was silly.

At a later date Frank utilized Anadrol-50 in down- ramping dosages the first 910 days of this protocol, to maximize potential due to a quick up-ramp in plasma androgen levels. For this example he used Anadrol-50 at the dosages of: Day #1-2 300 mg, #3-4 250 mg, #5-6 200 mg #7-8 150 mg, #9-10 100 mg of Anadrol-50. This advanced technique is sometimes referred to as front-loading and allowed for about a 28-30 day most effective period.

The androgenic dominance period of this example was about 75% with only a 25% anabolic dominance period. Later we will discuss methods of dosage utilization employed by Frank for long-acting testosterones that allowed for a shorter androgenic dominance period.

Example #1 B

Since Theramex has an active-life of about 20 days and half-life of 10 days, we know a single 250 mg injection would theoretically allow 12.5 mg to migrate into the vascular system daily. In example #1 A the 10-day administration period would therefore contribute 12.5 mg daily for each of the 10 injections. This means at the end of 10 days, the plasma level has been established at a threshold of 125 mg, theoretically. But it took 10 days plus to get there. The created advantage was a longer most effective period, and a slower androgenic down-ramp for the androgenic/anabolic transition.

In Example #1 B, we had doubled the daily Theramex dosage and cut the injection period in half by utilizing 500 mg each day for 5 consecutive days. This means each injection donated 25 mg daily to total plasma levels, again theoretically. The established plasma threshold was about 125 mg daily after day #5.

This was a single ramp Max Androgen Phase also. Since the androgenic activity down-ramped so quickly, a high anabolic/moderate androgenic AAS such as Deca Durabolin was a better transition choice in later protocols. This is because Deca is a little more androgenic in action than Durabolin. Deca has an active-life of about 14-16 days and half-life of 7-8 days. Deca Durabolin brand of nandrolone decanoate was usually dependable for a 15-16 day active-life. By beginning Deca on day #15 we were able to extend the 125 mg daily plasma level and most effective period to 25 days, or from about Day #5 to about day #30.

For other beasts, the initial 5 day period of this example has been quickly added into the 25 day most effective period by adding Anadrol-50: day #1-2 300 mg, #3-5 250 mg. Another option used was a fast/short acting testosterone such as Testosterone Propionate: Day #1-150 mg. This created a potential 28-30 day most effective period.

The androgenic and anabolic dominance periods of this example were about equal or 50% and 50%. But the androgenic to anabolic dominance transition could have been a little better. This would have mattered only when the example was utilized without other phase layers we will discuss as we continue.

Example #1 C

This was a double-ramp Max Androgen Phase. A double-ramp protocol uses one drug to establish a first plasma level or threshold, and a second drug to continue the dosage up-ramp effect to a second plasma level or threshold.

This was for very advanced athletes (which Frank was not, yet) since it exceeded the 1500 mg weekly total plasma level. As you will read several times, an effective plasma threshold exceeded before results ceased was a growth level wasted.

Looking at the rough graph you will see Theramex established a potential plasma level of 125 mg/d after day #10. Deca Durabolin continued by creating a second plasma level up-ramp until a theoretical plasma level of about 250 mg/d was reached after day #20.

Since Theramex has an active-life of 20 days, the first day's (day #1) Theramex injection "ran out" about day #21 and the high androgenic period began to ramp-down until day #30, theoretically. Of course the androgen period down-ramp was mediated by the high anabolic period, so the most effective period was about 10 days. But it would be crazy to assume the Theramex established plasma level of 1 25 mg/d beginning about day #10-11 was not highly effective.

The androgenic period up-ramp between days #1-10 was again later augmented to increase the most effective period by utilizing a short/fast acting androgenic. Several possibilities existed as you will see as we continue. However, I had a favorite for this example. Parabolan/trenbolone is seriously androgenic stuff. Day#1-228 MG, day #4-152 MG.

Another common beast utilized option for example #1C was the addition of a high anabolic /low androgenic such as Primobolan to create a second step in transition from high androgenic to high anabolic periods. This would have been best utilized if Frank was one of those athletes who either lost post-cycle lean mass more easily than others, or if he had suffered HPTA suppression on a serious level even when employing such brief protocols.

Instead of administering 200 mg/d of Deca only: Beginning day #1 6 Deca 150 mg/Primo D 50 mg, #17 Deca 100 mg/Primo 100 mg, #18 Deca 100 mg/Primo 100 mg, #1 9-20 Deca 0 mg, /Primo D 1 50 mg. No doubt some would say this was useless. I say they have not delt with the problem. This was about a 50%/50% ratio of androgenic/anabolic dominance period example.

The same 2 step transition was applied to example #1 B by a few other elite beasts: Day #1 7 Deca 300 mg/Primo D. 100 mg, #1 8 Deca 200 mg/Primo D. 200 mg, Day #1 9-20 Deca 1 50 mg/Primo D. 250 mg.

Example #1A has been adjusted to accommodate an intermediate athlete's needs by either cutting dosages in half or by utilizing the injections scheduled on days#1,3,5,7,9,20,22,24.

Example #1B was adjusted for the same athletes simply by cutting listed dosages in half. This provided a theoretical daily plasma level/threshold of about 62.5 mg/D.

"... which ain't no joke for an intermediate."

Cowchs

Each of these examples allowed Frank and other beasts to get in, grow hard and get out before the body could mount a full growth hating counter attack. With that said, let's go to the next page and check out Example #2, chart and description

DAY

A.

B.

C.

1.

Sustanon-250 250mg

Test Mix 250mg (B)

M/P Mix 250mg (D)

2.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

3.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

4.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

5.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

6.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

7.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

8.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

9.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

10.

Sustanon-250 250mg

Test Mix 250mg

M/P Mix 250mg

11.

Dura/Deca 250mg (A)

D/E/D Mix 250mg (c)

D/P Mix 250mg (E1)

12.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg

13.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg

14.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg

15.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg

16.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg (E2)

17.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg

18.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg

19.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg

20.

Dura/Deca 250mg

D/E/D Mix 250mg

D/P Mix 250mg

21.

D/P Mix 250mg (E3)

22.

D/P Mix 250mg

23.

D/P Mix 250mg

24.

D/P Mix 250mg

25.

D/P Mix 250mg

26.

Dur.250mg (Optional)

27.

Dur.250mg (Optional)

28.

Dur.250mg (Optional)

(A) Durabolin 50 mg + Deca Durabolin 200 mg

(b) Testosterone Propionate 50mg + Testosterone Enanthate 100mg + Testosterone Cypionate 100mg

(C) Durabolin 50mg + Equipoise 50mg + Deca Durabolin 150mg

(D) Masteron 50mg + Test Propionate 200mg (E1) Durabolin 100mg + Test Propionate 150mg (E2) Durabolin 150mg + Test Propionate 100mg (E3) Durabolin 200mg + Test Propionate 50mg

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.

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 ...

DAY

A.

B.

C.

1.

Sustanon250 1250mg

Theramex 500mg

T.S. 100mg (B)

2.

Laurabolin 500 mg

Theramex 500mg

T.S. 100mg

3.

Test. Prop. 200mg (A)

Theramex 500mg

T.S. 100mg

4.

Theramex 500mg

T.S. 100mg

5.

Sustanon250 1250mg

Theramex 500mg

T.S. 100mg

6.

Laurabolin 500 mg

Anadur 500mg

T.S. 100mg

7.

Test. Prop. 200mg

Anadur 500mg

T.S. 100mg

8.

Anadur 500mg

T.S. 75m g/W 25mg (C)

9.

Sustanon250 1250mg

Anadur 500mg

T.S. 75mg/W 25mg

10.

Laurabolin 500 mg

Anadur 500mg

T.S. 75m g/W 25mg

11.

Test. Prop. 200mg

T.S. 75mg/W 25mg

12.

T.S. 75m g/W 25mg

13.

T.S. 75mg/W 25mg

14.

T.S. 75m g/W 25mg

15.

T.S. 50mg/W 50mg (D)

16.

T.S. 50m g/W 50m g

17,

T.S. 50mg/W 50mg

18.

T.S. 50m g/W 50m g

19.

T.S. 50mg/W 50mg

20.

T.S. 50m g/W 50m g

21.

T.S. 50m g/W 50m g

22.

T.S. 25m g/W 75mg (E)

23.

T.S. 25m g/W 75mg

24.

T.S. 25mg/W 75mg

25.

T.S. 25mg/W 75mg

26.

T.S. 25mg/W 75mg

27.

T.S. 25m g/W 75mg

28.

T.S. 25m g/W 75mg

(A) Testosterone Propionate

(B) Testosterone Suspension

(c) Testosterone Suspension 75mg + Winstrol Depot (Injectable) 25mg

(D) Testosterone Suspension 50mg + Winstrol Depot (injectable) 50mg

(E) Testosterone Suspension 25mg + Winstrol Depot (injectable) 75mg

Example #3 A

Example #3 A: When looking at this example the reader should realize a few facts. First, that the example was utilized by a very advanced athlete and that a plasma level threshold of 250 mg/d was established very quickly. Second, that the dosage schedule allowed a better high androgenic /high anabolic transition than example #3 B (which also has been altered to accomplish the slower transition period for some applications in the past) and that the dosages as listed required a crazy injection site distribution to administer 35 ML of Laurabolin in one day.

What is interesting is that I had utilized this protocol at half the dosages while on a two week Mexican vacation with great success. Sometimes crazy things simply worked. However, some athletes (like Frank) who attempted this suffered serious oil trauma (which are flu like symptoms) due to the high oil volume introduced in such a brief period. I utilized the protocol by creating a Max Mix for days #2, 6, and 11 that allowed for a total of 20 ML on each day. Then site injected 2 ML into each bicep, tricep, lateral delt, calve, and outer pec. I did so after training chest/shoulders/arms on these days. Hey, I was on vacation! Again, I did this at half the listed dosages.

This example was a single ramp since we established the 250mg/d plasma level threshold up front. The androgenic/anabolic transition period ratio was about 40-60% respectively.

While in Mexico, I found some Fludestrin injectable 100 MG/ML, which is the injectable form of Teslac (Testolactone) and utilized 100 MG per day with 30 MG of Nolvadex before bed. This had some prolonged estrogen inhibiting effects long after discontinuance since I only used 0.5 mg/d of Arimidex for the rest of the protocols active-life. Faslodex (fulvestrant) would have been another long-acting injectable anti-estrogen option, but none was found.

So do the Math. Sustanon-250 has an active-life of about 20 days though some minor activity exists for a couple more days. Laurabolin has an active-life of over 26 days with a half-life of about 13 days. This example provided adequate androgenic stimulation until about day # 26-29 and excellent anabolic support for transition and mass gain solidifying effects until about day #32. So using two long acting esters together was quite effective when timing issues and chemical active durations were considered. Omnadren has been employed to replace Sustanon-250. But the stuff was often dirty.

I spent most of this vacation on the beach enjoying the sites. The rest was training, eating, and sleeping. This allowed me to travel to my next stop in the USA without chancing legal problems. Smuggling was and is a very bad idea. And why bother since it was not necessary?

The next example utilized Theramex and Anadur, which are both French AAS. I ran into a lot of both during my Mexican vacation if asked for by name. This of course provided another example of how to avoid legal issues when someone was living in, or traveling to, a less tolerant country. I have a friend who lives in Canada. He travels to France on business 3-4 times a year. He has a prescription for Growth Hormone and a doctor that treats him for "excessive estrogen accumulation". He is also smart enough not to destroy his career by getting involved in smuggling. He wears very large suits to his business meetings, by the way. Concerning the products I had encountered, the French spelling was Anador and the German and Swiss stuff was spelled Anadur.

This was the protocol my friend used for his trips to France. As you know, Theramex has an active-life of about 20 days and half-life of about 10 days. This means that the androgenic period of dominance was brief since Anadur has an active-life of 28 days theoretically, and a half-life of about 14 days. I liked Anadur for its high anabolic and protein sparing qualities. Unfortunately, it only came in a 25mg or 50mg/ml strength. This again was best utilized as a Max Mix for multiple site injections.

The example was a quicker double ramp protocol. Meaning the first substance established a plasma threshold and the second continued it. In this example, Theramex had established a 125mg/d plasma level after day #5 and Anadur continued the up-ramp until a second plasma level and threshold of 250mg/d after day #10. Obviously my friend was a very advanced athlete. (Who really should have been competing at high levels)

The example has been adjusted to a 125mg/d maximum plasma level by cutting daily dosages listed in half. (Duh). This was well below the 1500-1750 mg/week maximum AAS total plasma level I felt was the top for any beast including (and especially for) Frank N. Steroid.

This example provided excellent results and good high quality lean mass due to the prolonged anabolic dominance period. Sustanon-250 has been employed to replace Theramex to induce a quicker androgenic ramp. When that was the goal I have utilized the protocol as is for a very advanced athlete and added Testosterone Propionate to establish a rapid androgenic ramp and change the protocol to a single ramp: Day #1-200mg, #3-100mg, #5-50mg, or half that for the advanced 125 MG/D alteration.

This was a somewhat dirty protocol... but it worked so darn well! Both Testosterone Suspension and Winstrol Depot have an active-life of just about a day. So the plasma level threshold that resulted from this protocol was about 100mg/d by day #2.

Testosterone Suspension is the most androgenic Testosterone, in my opinion. The results from a 100mg/d plasma level realized with this example was about the same as a 125mg/d plasma level threshold from Testosterone Propionate. This is obviously due to the adjoined ester weight for the propionate.

Testosterone Suspension hurt going in and left the site area sore for a day or two. Winstrol Depot is actually a dirty drug due to its c17-alkylated structure. I have very rarely exceed 100 MG/D and then only for a period of no more than 21 days. Milk Thistle was a must with this drug for any beast who liked having a liver.

"A necessary note. There are those who wholeheartedly believed stanozolol

(Winstrol) in its injection form was not hepatic toxic at any dosage. I have reviewed Chemical Panels for many years and can say conclusively that the drug does cause liver stress at elevated and prolonged dosages without fail.

Personally I was amazed at the results this protocol provided. Especially when it was utilized site-specifically. Some of the most striated bodies in competition have been created by injecting each day's dosage directly into the muscle after it was trained (site specifically).

I have a theory as to why the results were so profound. It was simply due to the fast acting qualities of a water based product and the lack of an ester requiring the activity of esterase enzyme. The lion's share of the esterase enzyme exists in the circulatory system, not in muscle tissue itself. Therefore the free active form of an esterized drug has less effect upon site of injection but non-esterized drugs have the greatest localized effect.

Another effect was the synergy of IGF-1 production increase from c17- alkylated AAS during the deactivation process in the liver. This is also true site specifically in the case of non-esterized AAS due to muscle cell receptor interaction.

A second synergy exists between the Winstrol molecule and progesterone. Winstrol has a molecule structure very similar to progesterone. Progesterone is an estrogen of course, but it possesses androgenic qualities as well. However, even though Winstrol fits into progesterone receptor-sites, it does not activate estrogenic activity. Kind of like Nolvadex: it acts as an estrogenic antagonist to a certain degree, yet induces secondary androgenic effects through progesterone receptors. Unfortunately this can affect sex drive negatively.

When using Testosterone Suspension athletes needed all of the estrogenic-control possible. This example as listed was a great protocol for Frank when evaluating result potential: The androgenic dominance period and anabolic dominance periods are about a 50% equal ratio. The most effective period is about 28 days, and the system cleared within a couple of days after discontinuance. Too bad it was dirty.

When I wanted to increase the plasma threshold of Example 3C, I did not increase the dosages of Winstrol. I instead added Equipoise. Since the protocol had dramatic hardening effect over all (with good estrogen control), I preferred to add the Erythropoisesis stimulation effects of Equipoise. This increased red blood cell count and added to vascularity and muscle fullness. However, it was a mandatory factor to monitor CBC's so as to protect against platelet issues.

When I chose not to increase Testosterone Suspension dosages to accommodate the plasma increase from Equipoise, I choose Testosterone Enanthate. How was that done? Go back and look at example #2 B. I followed the schedule for Testosterone Enanthate as exampled and doubled the Equipoise dosages. The result was a 200mg/d plasma threshold level. I know several very advanced athletes who favored this layered combination for Max Androgen Phases.

We have discussed the single and double ramp plasma level examples developed for Frank N. Steroid and other beasts. For novice, intermediate, advanced or very advanced athletes, double ramp protocols were the best "transition" Max Androgen Phases. Instead of simply jumping to the next plasma threshold, double ramp protocols allowed an athlete to increase long-term growth potential by utilizing both their prior threshold and the next step. Think about it.

Other Max Androgen Phase Examples?

Of course there many examples of Max Androgen Phases possible including layered, multi-staged, single and double ramped...and others.

3 Stage Max Androgen Phase

DAY

DRUGS

DAY

DRUGS

1.

Test Cypionate 200 mg + Test Propionate 100mg

22.

Boldenone Undecylenate 100mg

2.

23.

Boldenone Undecylenate 100mg

3.

Test Cypionate 200 mg + Test Propionate 100mg

24.

Boldenone Undecylenate 50mg + Nandrolone Decanoate 150mg

4.

25.

5.

Test Cypionate 200 mg + Test Propionate 50mg

26.

Boldenone Undecylenate 50mg + Nandrolone Decanoate 150mg

6.

27.

7.

Test Cypionate 200 mg + Test Propionate 50mg

28.

Nandrolone Decanoate 200mg

8.

29.

9.

Test Cypionate 200 mg + Test Propionate 25mg

30.

Nandrolone Decanoate 200mg

10.

31.

11.

Test Cypionate 200 mg + Test Propionate 25mg

32.

Nandrolone Decanoate 200mg

12.

33.

13.

Boldenone Undecylenate 100mg

34.

Nandrolone Decanoate 200mg

14.

Boldenone Undecylenate 100mg

35.

15.

Boldenone Undecylenate 100mg

36.

Nandrolone Decanoate 100mg + Trenbolone Acetate 50mg

16.

Boldenone Undecylenate 100mg

37.

17.

Boldenone Undecylenate 100mg

38.

Trenbolone Acetate 100mg

18.

Boldenone Undecylenate 100mg

39.

19.

Boldenone Undecylenate 100mg

40.

Trenbolone Acetate 100mg

20.

Boldenone Undecylenate 100mg

41.

21.

Boldenone Undecylenate 100mg

42.

Trenbolone Acetate 100mg

• Day 43-56 T-3 25mcg 2xd, Clenbuterol 80-120mcg 1xd, PCF-2a 1 mg 2-4xd, Clomid 50mg/d

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Chemically Engineered

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