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There are two types of anabolics:Class-I)These are mostly the oil-based injectibles.They work primarily by binding to and activating the androgen receptor,which then interacts with your DNA,sending out various signals to impact anabolism/anti-catabolism.Class-II)These are primarily 17alpha-alkylated oral compounds.They,unlike their oil-based counterparts,do not bind well to the androgen receptor,and acheivetheir effects on growth/strength independent of this process,by binding to other types of receptors.The above study just offers some actual scientific proof into this,and sheds light on why it is beneficial at times to stack steroids from opposing groups,so as toget the maximum results through multiple pathways,as opposed to one primary mechanism...So basically it means you should stack a Test (whatever ester), a 17aa steroid, and maybe if you want some other type of Class 1 steroid. For optimal results.This is basically common sense, but good that there is scientific results to back it.Nothing puts mass on as efficiently as it,except for maybe tren.But unlike tren,testosterone only has ‘mediocre’ binding capacity to the A/R,being far outshinedby deca and primo in the binding capacity department.Yet it provides much better overall growth.Why?It outshines the above aforementioned anabolics in theClass-II mechanisms,such as influences on GH,IGF-1,activation of satellite cells into full maturation,activation of prostaglandin receptors,etc...I believe that non-A/R mediated activity is UNDERRATED if anything on it’s influences on growth.Man child-That’s exactly right.There are two steroids that possess DUAL activity(both class-I & II),and that is testosterone and tren.For this reason,they shouldform the base of your cycle.Tren has the strongest binding capacity to the androgen receptor of ANY steroid,therefore adding a class-I with it probably isnt necessary,as it’s more than sufficient in that department.It’s class-II activity isn’t as aggressive ,therefore adding in a class-II oral such as winstrol or dianabol wouldwork very well.As for testosterone,,the same applies.Throw in an oral compound and a class-I,such as deca,eq,or primobolan,and you’ve got all the bases foranabolism completely covered.Now all you need is the right training stimulation ,and ample nutrition, and you’re on your way to explosive growth...Your wish is my command, lol...Anabolic Steroids achieve their effects on hypertrophy through different mechanisms,and as such are classified into two different categories,class-I and class-IIcompounds.I will explain which ones work through which pathway,and how to effectively combine opposing groups to maximize potentiation of one anotherfor explosive growth....Class-I-These are steroids who’s primary influence on anabolism is achieved through aggressive binding and activation of the androgen receptor...Examples ofpotent class-I’s are-Deca-durabolin,primobolan,equipoise,oxandrolone...Class-II-These are compounds with potent activity independent of A/R binding/activation,and their activity has been monitored in neuron’s,microsomes,mitochondria,etc...Examples of potent class-II’s are-Anadrol,Dianabol,winstrol,Fluoxymesterone...Then we have steroids that are potent combination steroids all by themselves(meaning they display influences on growth through both class-I and II activity,andthus are very effective as’stand-alone’anabolic agents as well as forming the ‘base’ of most steroid stacks)....Two compounds possess this unique characteristic-Trenbelone and Testosterone.Either of these two steroids should form the base of most users stacks,as the cover both A/R and non-A/R mediatedmechanisms,and adding to them with either a class-I or II will only potentiate that particular mechanism towards muscular hypertrophy...Now that we’re aware of which compounds work through which mechanism, how do we combine them effectively to maximize each one’s potential?Asexplained above,Testosterone and trenbelone should form the base of any serious steroid stack,but great effects can be had by combining single mechanismsteroids from opposing classes....
Examples of this type of synergistic combining could be(but are not limited to)

CUTTING:
Winstrol & Equipoise
Winstrol & Primobolan
Fluoxymesterone(Helotestin) & Equipoise or Primobolan

BULKING:
Deca & Dianabol
Anadrol & Equipoise or Primobolan
Winstrol & deca....

And of course,using test or tren as the base compound for either cutting or bulking will only make results that much more explosive. If using test forcutting, an anti-aromitase should be incorporated.

RECEIPE FOR LITTLE MONSTERS

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RECEIPE FOR LITTLE MONSTERS


The following are just one example of an elite members usage and ideas: Do not think these drugs and usages are written in stone. Different things work for different people. Start out slow with smaller doses, and work your way up.
**********

Testosterone 400-800mg every day - the different names are for the different esters attached to the test molecules. I believe the scale from fastest acting to slowest release in your body is this: suspension (water based), propianate, phenylpropianate, enanthate, cypianate, isocaprianate, decanoate. Longer acting ones take time to release, and stay in your system longer, and also tend to retain more water. Faster ones I have heard tend to be more painful, but it also depends on the benzyl alcohol inside.

Trenbolone Acetate 50-75mg every day. (Fina - best when injected and comes in premade injectable form or pellets that you make the solution with). Tren and Test are the foundations for every cycle, either cutting or
bulking.

Equipoise 400-600mg every day - a derivitive of the test, and makes you
hungry as shit, helps put on maintainable weight, makes your veins stick out more, and adds size.

Anadrol 50 - definitely one of the strongest, but also harshest chemicals
out there. You will blow up on this, but don't take for more than a few
weeks as the side effects are almost not worth the benefits. Also, you will
lose much of your gains with this unless you follow up correctly. Anadrol
must be accompanied by winstrol or RU-486 in order to prevent progesterone related effects.

Dianabol - dbol: this is a great kickstarter if you want mass, but not as
good for cutting. It will make you retain a lot of water quickly, but you
will also lose this water when you finish it. you will get great size,
strength from this, too.

Winsrol - ideal for cutting, but only when used with proper diet. Does not
make you retain water, hurts like hell to inject, can be taken orally, and
gives you amazing strength gains. If used with diet, most say they get
ripped up and lean on this.

Primobolan Depot - more for cutting and bridging, not mass building.
Reminds me of Abercrombie guys - lean, cut, but not very big overall.
Anavar - oral aa17 drug, very expensive, but everyone says is worth it.
I've heard of great gains, ideal fat loss, but not sure about strength.


For protein - I don't like meal replacements cause they fill me up. but if you do, myoplex tastes good to me. I love isopure the most for no-carb protein, but very expensive.

For diet and timing do this:
oatmeal in morning, egg whites, cranberry juice/water, maybe a small protein shake. Later on do cardio if you want to cut up. Eat 6-8 smaller meals spaced evenly through day rather than 3-4 huge meals. This will help speed up your metabolism and help digest the nutrients better for more effective use.

DO NOT EAT ANY SUGARS OR SIMPLE CARBS WITHIN AN HOUR OF WORKING OUT!!!
If you do, your pancreas will release insulin to break it down, the insulin tells the ATP to stop converting to ADP releasing energy, and if you work out, you won't get as effective training and results. When ATP converts to ADP, a phosphate molecule is released providing energy to flex your muscle - this happens millions of times at once when flexing. Then the phosphate molecules reattach to ADP to form ATP again. Insulin counteracts that.

DO EAT SUGARS AND SIMPLE CARBS IMMEDIATELY AFTER WORKING OUT!!!
This will release the insulin, stop the ATP ADP cycle, and allow your body to get energy from the sugars rather than from burning protein (which is needed to rebuild muscle). Also, you want to replace your glycogen stores for your next day's workout. Add L-Glutamine to your Gatorade or Cranberry Juice to help aid in muscle recovery.

DO DRINK A LIQUID PROTEIN SHAKE WITHIN 30 MINUTES OF WORKING OUT!!!
This is when your body is starving for protein. Try to get 50g of liquid protein. If you eat solid instead, it won't get absorbed as quickly or easily.

DO EAT A GOOD MEAL WITHIN AN HOUR OF WORKING OUT.
You may be full from drinking the cranberry juice after the workout, then the protein shake, but now you should add in your complex carbs such as brown rice, oatmeal, possibly pasta.



ANADROL-50

ANADROL-50: R750.00/50 tabs R1300.00/100 tabs

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Anadrol was the U.S. brand name for 50mg Oxymetholone tablets, which were available in the U.S. until 1993. Syntex is the world producer of this drug, and markets it under a few different brand names in other areas. Oxymetholone is a 17alpha alkylated oral steroid. Second to none, this product is generally considered the most powerful steroid available. Anadrol will produce extremely dramatic weight and strength gains in its user. Some of this weight and strength
gain will be due to the drugs heavy water retention. Users of Anadrol report severe crashes when stopping usage, mostly due to the loss of water and inhibited endogenous hormone production brought about during the cycle. Aside from the water, Anadrol will pack on the mass like no other steroid. A short cycle of Anadrol could account for a gain of over 20lbs in many users, sometimes more. As this drugs anabolic properties are so extreme, so are it’s androgenic side effects. Due to the strength of these side effects, Anadrol should never be used by women. For starters, oxymetholone will easily convert to estrogen and DHT. As stated earlier water retention will be present, along with an increase in blood pressure. Kidney functions may also need to be looked after during longer use. Hair loss has also been reported among users with a predisposition for male-pattern baldness. The most dangerous attribute of Anadrol is that is it 17alpha alkylated. As you probably know 17aa orals are toxic to the liver. Unlike Dianabol (another popular 17aa oral) which is effective in doses of as little as 15mg, Anadrol users generally start with 50mg/day and often lead up to 150mg/day. So when a user takes 3 Anadrol tablets, his liver is processing roughly the equivalent of 30 Dianabol tablets. This obviously is quite a lot of 17aa steroid for your liver to process, so it is pertinent a user has his liver enzymes checked regularly with a doctor. When you hear of horror stories involving liver cancer from steroid use, Anadrol is most often the culprit. For medical treatment, Syntex recommends 1-5mg/kg of bodyweight per day. This leads many patients to take as many as 8+ tabs per day, for extended periods of time. This is much more than an athlete would need and should be using, which may be why documented cases of liver cancer seem more prominent among non-athletes taking Anadrol medically. Lately, many people are speculating on how long this product will be available worldwide. Syntex has stopped production of Anadrol in the U.S., Oxitosona in Spain and medical use in other areas of the world seems to be declining due to the advent of newer drugs to treat conditions in which Anadrol was formerly used. Aside from the Mexican version, all other forms of Anadrol are now being counterfeited, often with incredible accuracy. In the U.S., a version of the now unavailable American Anadrol has been found in which box, bottle and even the stamping of the tablet are identical to the real version. The only seen difference
is the lack of active ingredient. Since real U.S. Anadrol has been out of production for some time, it would be safe to say anything labeled Anadrol is fake. Anapolon is copied as well with good accuracy. Oxitosona was/is counterfeited but since Syntex dropped its production in 1993, all forms should be considered fake. Hemogenin from Brazil is another popular version, which makes its way to the states and is also counterfeited. Currently, all the loose red Anadrols from Mexico (Stamped with SYNTEX on one side and 2902 on the other) which are circulating the states should be considered real. They are available only to clinics and hospitals in Mexico, so black market supplies are limited. Reports are that they may also be slightly underdosed.

ANAPOLON

ANAPOLON: R600.00/50 tabs R1000.00/100 tabs

Anapolon has been the strongest, oral steroidal compound, which is a derivative of dihydrotestosterone that has been currently only available for institutional use in Mexico. Clinically, Anapolon had been often prescribed in efforts to have treated anemia, which had been caused by deficient red cell production. The androgenic and high anabolic properties of Anapolon have been substandard of Testosterone, which had pertained this compound to have also been a dramatic muscle building product. Many athletes had claimed that strength and weight increases had been very substantial within a relatively short period of time. This characteristic had allowed the compound of Anapolon to have been a very popular choice of oral steroidal compounds amongst many athletes, primarily those of the male gender. Most athletes had frequently experienced a general weight increase of approximately 10 to 15 lbs. or more, within two weeks with the administration of this compound. This of course, had been largely attributed to the tremendous amount of water retention, which had immediately increased the muscle diameters, which in turn, had permitted a rapid increased size appearance. Consequently, this retained amount of water in the muscle cells and joints, had also additionally provided a smooth appearance, as the size increase had been quantitative, not qualitative. An advantageous effect of the water retention however, had been the ability to have eliminated, or having soothed associated joint problems, which had been due to this side effect’s subsequent lubricating quality. This had often been appreciated by most athletes, as this characteristic had frequently allowed for intense workouts, which had often been previously somewhat restricted, due to associated aggravated pain in the joints. The Anapolon oral steroidal compound, had further increased the number of red blood cells, which in turn, had enabled the muscles to have absorbed more
oxygen. This had generally resulted in the muscle being able to have endured more physical stress, which had been due to the significant increase in blood volume. A “pump” effect had often been experienced when training particular muscles, and had even become somewhat painful to the extent, that the performed exercise had frequently been required to have been abandoned, in order to have alleviated this sensation. However, this perception of increased strength and power had commonly been desired by all athletes who had practiced the self-administration of this compound, as this sensation had usually been indicative that the compound of Anapolon had indeed, been performing to it’s full capacity. Several athletes had also claimed that another distinguishing trait of Anapolon, had been the increased training duration’s, as this compound had been able to have stimulated the regeneration of the body, which often had enabled further muscle-building progress, and had stalled the possibility of over4raining. However, although the substance of Anapolon had been powerful, it unfortunately, also had imposed the highest threat for serious adverse reactions out of any oral or injectable steroids compounds. A few athletes had experienced excessive water retention, which had sometimes resulted in high blood pressure.
Anapolon has very high DHT levels, and had been very toxic to the liver, due to the characteristics of being a C-17 alpha-allrylated steroid. Although the Anapolon steroidal compound had been known for quick strength and mass gains, it’s utilization had not been suitable for novices, and had only been used by some athletes after a certain development had been achieved; or consequently, the prior use of weaker steroid compounds had been experienced.

ANAVAR

ANAVAR: R600.00/50 TABS


Also under the name Lipo-Dex and Nilavar. Anavar is manufactured by searle lavatories under the brand name, and by spa labs under the generic name Oxandrolone. The brand name drug is made under a certain number of loss per year. This if it sells out before the end of the year, the product just disappears. Searle does not make more until the next term. This keeps the price of anavar high, and availability low. Anavar is typically prescribed on a 2 - tablet, twice daily routine. The drug is better absorbed when taken right after meals. Woman have started with one tablet twice daily. This is thought to be the optimal dose for woman. The drug can be used in combination with other steroids for optimum results after a plateau is reached on the anavar alone. If some size is required, but no injection is desired, dianabol or anadrol can be combined with the anavar. Here the user would add 1 dianabol tab twice daily or a half anadrol twice daily. Later, and for greater size, going to 4 dianabol tabs, or to anadrol per day has worked well . for greater gains the user would add an injectable steroid to the cycle instead of the previously mentioned orals. The injection would vary from deca for cutting, to testosterone for weight and strength gains. Research shows that anavar is the one anabolic steroid least likely to cause any side effects . there are very rarely reports of ill effects of any kind using anavar . there is seldom any fluid gains with this drug, which makes it the drug of choice with potential blood pressure problem uses . anavar is also good trade for persons who need to keep their weight down, either for cutting or like a powerlifter who needs to make weight . Thus you will see a number of bodybuilders using anavar the last two months before competing. Some powerlifters claim that this steroid is No. 1 for gaining strength without water weight. The use of the low androgenic product is quite popular with women. Very little masculinisation in any form have been seen among woman who have used this trade at a dose of 5 mg daily. Most women start out on 1 tablet per day and go up to three tablets daily. The dosage of 5 mg of anavar per day has worked
out to be the optimum. The first signs of virilisaton could include persistent hoarseness, deepening of the women’s voice, acne, decreased libido, and/or clitoral enlargement. If any of these symptoms should show, the woman should get of the trade immediately. Anavar will not aromatize. This means of course it’s one of the very few anabolic steroids that will not convert to estrogen at any dosage. This means it will not cause that soft look to the muscles or will it lead to the development of breast tissue in men. Some persons will convert much more of a steroid to estrogen than others. These people can use a dosage starting with 2 tabs twice daily, and reaching a maximum dose of .1 MG of the add per pound of body weight. Often the user plateaus on the drug alone, he might add a small dose of deca that would not aggravate any existing gynecomastia. Or a daily dose of 10 MG of halotestin could be added to the anavar cycle to
increase strength and hardness, while having no aromatize in effect. Anavar is a multi-purpose steroid. Its very low toxicity makes it safe to take, even on lower cycles. It is advised that a high protein diet be maintained while taking anavar to insure its effectiveness. It is been counterfeit under the Spa label. Watch for the Searle liable to be safe.

ANDROXON 40MG

ANDOXON: R650.00/60 tabs
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Androxon: (testosterone undecanoate) 40mg caplets. 60/bottle. Seen with the names Andriol, Understor and Restansol in Europe. This oral steroid is quite different. It comes in small oval shapes red caplets. They are usually contained in foil templates that caplets are put out of. An oral form of the product is contained in these caplets. Androxon is not an Alfa alkalated 17 steroid
which means it is not toxic to the liver. The side effects of using the asteroid are therefore not what they are with the other oral steroids. Androxon is contained in a natural ester Base, which is very easy on the system, but does give the steroid only a small amount of time in the blood. The trade itself is a very high androgenic and anabolic steroid. Strength and weight gains on this product are reported to be very substantial. It also has very good glycogen retaining qualities.
All in all androxon seems to give all the gains of other testosterones, while been safer to use. It has begun to replace some of the other steroids once so popular. The androxon does not suppress the body’s own testosterone production nor aromatize when dosages are kept below 280 mg a day. An average effective dose of this drug seems to be in the range of 200-MG daily. A person taking this drug should be sure to space out the dosages as much as possible.
For instance if one were using 120 mg daily, he would want to take one captured every eight hours to get the optimal effect. The only bad news about androxon is that the price is quite high and availability in certain countries are limited.

BOLDEBOL-H

BOLDEBOL-H:R480.00/10ml vial
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Equipoise: Brand Names: Boldebal-H, Equipoise, Ganabol, Maxi-Gan, Pace, Sybolin, Vebonol,
Description: 50 mgs. / cc. 10ml vials. Boldenone undecyclenate is a very popular steroid. This steroid is only available legally at a veterinarian clinic. Equipoise is a highly anabolic, moderately androgenic steroid. For this very reason, it is typically taken in a stack with other steroids like testosterone if you are on a mass cycle or perhaps with winstrol if you are on a cutting cycle. The main benefit of taking equipoise is that it increases protein synthesis
in the muscle cells. This effect is very similar to what you would experience while taking anavar. Equipoise gives you slower but much more high quality gains in muscle as opposed to the normal “quick” muscle gains that you would expect from a testosterone. This is not a steroid to take on its own and expect 20 lbs. in 6 weeks. It is just not going to happen. You can expect around 3 weeks before you start seeing results and they are not going to be staggering, but will be “more permanent” than any gains you would get from any of the multiple testosterones that are available. This steroid stays active in the system longer than most of the testosterones as well. This makes equipoise a poor choice if you run the possibility of being drug tested. Equipoise is very common in the precontest arena for two main reasons. First off, there is a low amount of aromitization and secondly there is very little water retention while taking equipoise. This makes equipoise a good precontest steroid. Equipoise is well known to give a good increase in the pumps you get while working out. This is caused from the increase in red blood cells that you will experience while taking this steroid. Equipoise is also well known to help cause a dramatic increase in appetite. When taken with a good mass building steroid like dianabol, this is a sure formula for successful gains in muscle mass. Side Effects: This list by no means states that you will get all these side effects, but there is a possibility to get any or several of these side effects. I continually get emails requesting to know the side effects that are possible, so here is the list of possible side effects. Equipoise is generally a little safer to take than the testosterones, but you will tend to feel ill for a few days after injection. This ill feeling is similar to flu-like symptoms and will go away after a few days. This side effect is similar to what people feel when taking Sustanon 250 as well. Other known side effects consist of: nausea, leukopenia, symptoms resembling a pepticulcer, acne, excitation (commonly referred to as roid rage), sleeplessness, chills, vomiting, diarrhea, hypertension, prolonged blood clotting time, increase in libido. Females had reported: menstrul irregularities, post-menopausal bleeding, increased sex drive, swelling of the breasts, hoarseness or deepening of the voice, and enlargement of the clitoris. Men had reported: acne, gynocomastia, and increased aggression. Effective Dose: 150 - 300 mgs. / week. Equipoise shots are typically taken twice a week. Street Price: R480.00/10 ml vial. Equipoise is commonly pretty expensive on the black market and counterfeits are plentiful. Equipoise always has a slight yellow color as well, so keep your eyes open if someone is trying to sell it to you and use your head. Stacking Info: Muscle hardness enhanced with Parabolan, Halotestin, or Winstrol, for mass stack it with Anadrol, Dianabol, or Sostenon 250.

CYPIONATE

CYPIONATE 250: R380.00/10ml vial
(testosterone cypionate) 250mg/ml/10cc/vial

This is an oil based injectable form of testosterone. It is high in androgens and is very anabolic as well. Depo-Testosterone aromatizes quite easily. Water retention is often a problem when this drug is used. It is only moderately toxic to the liver, but can cause a marked disturbance in the body’s endogenous production of testosterone. Depo-test is often a dramatic size and strength building drug. It can be stacked with a number of steroids and come out to be a great bulking
cycle. This drug is the most popular testosterone used by athlete. Although the gains a person can make on testosterone’s are dramatic, the size and strength lost when the drug is stopped is also dramatic for most. This can be compounded by the body’s suppressed endogenous testosterone production. Some users have minimal losses if they take Nolvadex throughout the cycle, come off the drug very slowly, and take HCG right after the cycle. When taken in moderate dosages, its gains can outweigh its down side. Effective dosages for men are in the range of 1cc to 3cc per week, women should not be using any testosterone.

CLOMID

CLOMID:R230.00/10 tabs

(estrogen receptor antagonists) Estrogen receptor antagonists, more simply referred to as anti-estrogens (though this term is often loosely applied to all estrogen maintenance drugs), are drugs
that block estrogens from exerting activity in the body. This is actualized by the ability of a particular substance to bind to a segment of the estrogen receptor, yet not activate it. This in turn prevents other estrogens from binding and activating the same receptor site. In a clinical setting an estrogen antagonist, most prominently the drug tamoxifen citrate (sold under the brand name Nolvadex) is typically used as the first line of defense during advanced breast cancer therapy. Its use can efficiently deprive estrogen responsive cancer cells of necessary hormone, allowing a high rate of response in patients with such forms of cancer. Stronger agents such as aromatase inhibitors (discussed below) are usually a second choice, substituted when conventional antiestrogen therapy fails to elicit the desired response. A drug like tamoxifen is preferred over other agents as the first course of breast cancer treatment for a number of reasons, most due to the fact that that it is both extremely effective yet does not inhibit the actual formation of estrogen in the body. Among other things, this may allow Nolvadex therapy to be somewhat more comfortable for the patient. Although many women (particularly pre-menopausal) seem to suffer menopausal-like side effects with virtually all estrogen
maintenance drugs, estrogen antagonists are often somewhat more tolerable than agents that block the synthesis of estrogen. In fact the activity of tamoxifen is itself variable, such that in certain target tissues it may actually act as an agonist (activator) of the estrogen receptor. It therefore does not completely diminish the biological activity of estrogens, though it does considerably reduce it nonetheless. It is also well understood in medicine today that estrogens play a supportive role in the cardiovascular system. For example, studies show that a rise in the
estrogen level (as in post-menopausal estrogen replacement therapy) is typically linked with a reduction in LDL (bad) cholesterol, and a rise in HDL (good) cholesterol. The ability of tamoxifen to act as an estrogen agonist in the liver likewise gives it what may be its most welcome property, namely that it exhibits an estrogenic, rather than antiestrogenic, effect on blood lipid (cholesterol) values. As a 1998 study by the Department of Clinical Oncology in the Netherlands
Cancer Institute shows, during long-term treatment with tamoxifen (6 months) a lowered LDL cholesterol level, and significantly elevated HDL cholesterol level and HDL-C/total-cholesterol ratio may result. This trend should reduce an important risk factor for heart disease, obviously a welcome effect during treatment. For the steroid-using athlete already faced with negative alterations in lipid profiles, such an effect could obviously an important consideration.
Clomid (clomiphene citrate) is very similar in structure to Nolvadex, both drugs being classified as triphenylethylene compounds and used clinically for similar purposes (breast cancer as well as female infertility treatment). As well as we see with Nolvadex, Clomid is a partial agonist/antagonist of the estrogen receptor depending on the target tissue in question. Although athletes most commonly think of Clomid as a testosterone-stimulating drug only (another effect of antiestrogenic compounds), to be used at the conclusion of steroid treatment, its activity in the human body is not at all dissimilar to Nolvadex. It should likewise be thought of not as a drug with its own niche of use, but instead as another efficient remedy for gynecomastia similar to Nolvadex (with the related ability to support the release of testosterone). It could clearly replace Nolvadex as a preventative measure against gynecomastia during cycles with aromatizable steroids without noticeably altering the level of effect received, just as Nolvadex can be used effectively to increase the synthesis of testosterone in the body at the conclusion of steroid use (though admittedly Nolvadex may be slightly more potent in both regards)

CLENBUTEROL

CLENBUTEROL:R300.00/50 tabs
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Brand Names: Broncodil, Broncoterol, Cesbron, Clenasma, Clenbuter.Pharmachim, Contrasmina, Contraspasmina, Monores, Novegam, Oxyflux, Prontovent, Spiropent, Ventolase, Ventapulmin,
Description: Is available in 10 - 20 mcg tablets or in the .016 mg/gram Ventapulmin Vet variety. Clenbuterol is known as a sympathomimetic. These hormones are taken to mimic adrenaline and noradrenaline in the human body. Clenbuterol is a selective beta-2 agonist that is used to stimulate the beta-receptors in fat and muscle tissue in the body. Clenbuterol exhibits most of its effects on the stimulation of both type 2 and 3 beta-receptors. Clenbuterol is really one of bodybuilding’s most misunderstood performance enhancement drugs. It is true that it is effective in helping to burn bodyfat but it is often been stated that clenbuterol is effective in causing anabolic gains and has in times even been compared to some of the weaker anabolic steroids. Books such as the World Anabolic Review, 1996, by P. Grunding and M. Bachmann state incorrectly that, “its effects, however, can by all means be compared to those of steroids. Similar to a combination of Winstrol Depot and Oxandrolone....” These statements are inaccurate and misleading to say the least. A lot of these claims as to the anabolic effects of clenbuterol are derived from studying the effects of clenbuterol on livestock. Clenbuterol is effective in increasing muscle mass and decreasing fat loss in animals. The problem with the variation in anabolic effects between humans and livestock is that livestock have an abundance of the type 3 beta receptors whereas humans have little if any of the type 3 beta receptors. These beta-3 receptors increases insulin secretion and sensitivity, causing more glucose and amino acids to be transported into skeletal muscle thus causing the anabolic effects that we, humans, just aren’t seeing. As Dan Duchaine stated in his Muscle Media article on clenbuterol, “In those animal research studies showing an anabolic effect from clenbuterol, it’s my guess the anabolism happens specifically when the beta2 receptor stops working. At that point, the beta3 increases and causes the anabolic effect through insulin mechanisms.” Since humans, again, have either very little or no beta-3 receptors, there is no chance of this anabolic effect. Just another of the studies where everyone assumed that what works in animals must work in humans. This is just simply not the case with clenbuterol. Clenbuterol does work effectively as a fat burner though. It does this by slight increases in the body temperature. With each degree that the temperature in your body is raised from the use of clenbuterol, you will burn up approximately an extra 5% of maintenance calories. This makes it effective as a fat burner. Your body will fight this by cutting down on the amount of active thyroid in the body as well as through beta-receptor down regulation, which explains why you only have a limited effective period to take clenbuterol. While I am on the subject of beta-receptor down regulation, I would like to dispose of another myth. This
involves the two on/two off cycling theory that I believe was originated by Bill Phillips in the Anabolic Reference Guide and has somehow made it’s was into every other steroid book since then including the WAR and Physical Enhancement with an Edge. The two on-two off theory simply will not work because of one main reason: the half life of clenbuterol. This 2-on/2-off idea was a THEORY ONLY, not by a doctor or scientist, and not based on specific knowledge of clenbuterol, but derived by imitation from other drug’s with shorter half lives.
Clenbuterol has been reported as having a half life of about 2 days, but that is not actually correct, since it has biphasic elimination, with the half-life of the rapid phase being about 10 hours, and the slower phase being several days. Supposedly, this is one of the reasons the FDA never approved clenbuterol as an anti-asthmatic drug...the FDA frowns on drugs with long half-lives if drugs with more normal half-lives are available. So with a 2-on/2-off cycle you never have time to get enough of the clenbuterol out of your system for this theory to be reasonable. In actuality, it probably hasn’t even dropped to 50% of your peak concentration before you are taking the drug again. With this all taken into account, there is no reason to think that this cycling would significantly reduce the problem of receptor desensitization. A more reasonable approach would be either one week on, one week off, or alternately, two weeks on two weeks off. The
two week cycle has the disadvantage of a “crash” period afterwards. This crash period can be helped with the use of ephedrine to lessen the lethargy that you will experience.
If you are interested in taking clenbuterol for anything other than fat loss then you might as well stay away from this compound. There is a lot of talk as to how clenbuterol compares to ephedrine as well. Most “experts” feel that clen gives a better bang for the buck than the ECA stack. It should be noted that clenbuterol’s results and effects are much shorter lived. They work through very similar mechanisms. Both products stimulate the beta-receptors but clenbuterol seems
to be a more refined version, called a second generation beta-agonist drug, than ephedrine. Clenbuterol targets the proper receptors, being the beta-2 and 3 receptors than ephedrine more specifically which should in theory make clenbuterol more effective of a fat burner. Again, most of the so called “experts” say that clenbuterol is more effective than ephedrine. I, personally, get worse results with clen vs. the good old ECA stack. Clenbuterol also didn’t blunt my hunger
either and I ate more while taking it as well. I also seem to get much better effects out of cytomel as a fat burner as well. Even better than the ECA stack or clenbuterol. But, again, that is my personal opinion. Effective Dose: 80-140 mcgs. / day in split doses throughout the day. Anything over 140 mcg a day is overkill since the beta receptors can only take so much of a product and then more is just wasteful. Street Price: R300.00/50 tabs.
Stacking Info: One week on, one week off might make sense, or alternately, two weeks on two weeks off makes sense but has the disadvantage of a “crash” period afterwards. You can take ephedrine after the clen to help reduce this “crash” period or at least make it more bearable for you. The two on/two off theory is absolute bullshit and can’t work; read above.

DECA-DURABOLIN OR DECA-300

Deca-300 & Deca-Durabolin
SA Deca:R850/6 amps
Pakistan Deca:R600/10 amps
Deca-300:R950.00/10ml vial


Brand Names: Anabolicum, Anabolin LA-100, Anaboline, Androlone-D 200, Deca-Durabolin, Deca-Durabolin 100, Depo-Nandrolone, Dequibolin-100,Elpihormo, Extraboline, Hybolin Decanoate, Jebolan, Kabolin, Nandrolate, Nandrolone Decanoate, Nandrol Decanoate, Nandrobolic L.A., Neo-Durabolic, Norandren 50, Norandren 200, Nurezan, Pri-Andriol LA, Retabolil, Retabolin, Sterobolin, Turinabol Depot, Ziremilon, Description: Deca can come in many different strengths: 25, 50, 100, and 200-mgs/cc varieties., no oral versions of Deca produced. Deca-Durabolin is probably the all time most popular steroid (except for maybe Dianabol if you could actually find some). Deca produces very few side effects. It is easy on the liver and promotes good size and strength gains while reducing body fat. Deca-Durabolin is highly anabolic and only moderately androgenic. It works by promoting a positive nitrogen balance in the body, which causes the muscles to be able to use more protein, more efficiently than normal. It does this by causing the muscle cells to store more nitrogen than they are releasing. With this positive
nitrogen balance, the muscle cells will be able to use more protein than they usually can. If you don’t eat and sleep enough though, the magic will not happen. It takes three days after injection to dissipate from the site and stays active in the body for about 17 days. Gains will go away very slowly after the cycling period if workouts are kept intense. Deca is the worst steroid that you can take if you run the chance of being drug tested. People have been known to test positive
up to 1 1/2 years after the last shot. This is a very long time. Keep this in mind if you are in the NCAA or some other organization where you run the risk of being tested. Side Effects: Deca-Durabolin is a relatively safe steroid. Typically, you can expect a little minor acne, higher blood pressure that causes a longer time period for blood to clot, headaches, and increased libido. Any of the following are also possible though: nausea, leukopenia, symptoms resembling a peptic ulcer, acne, edema (water retention), excitation (commonly referred to as roid rage), sleeplessness, chills, vomiting, diarrhea, hypertension, prolonged blood clotting time, increase in libido. Females had reported: menstrual irregularities, post-menopausal bleeding, swelling of the breasts, hoarseness or deepening of the voice, enlargement of the clitoris, and water retention. Men had reported: cases of impotence, chronic priapism, epididymitis, inhibition of testicular function, oligospermia, and bladder irritability. Effective Dose: 400 - 600 mgs/week. Some people say you can get away with less but I have not found that to be true at least with myself. It is easy on you, so I would tend to go the extra mile and take a little more when I can find it.
Street Price: R600.00/10/1ml vials at 50mg/ml Organon Pakistan, to R850.00/6/1ml vials at 5omg/ml Organon SA . This steroid is without a doubt the most common one that is counterfeited. You need to check for all the telltale signs, like being able to twist the metal top; you should not be able to turn it by hand if it is real. You should not be able to scratch the label off easily with your fingernail either. Another common trick is the date. It should be obviously stamped on the bottle. Commonly, counterfeits have the expiration date printed on the label in the same color ink as the rest of the label. It can be black but you can tell a stamp from something that was printed on the label at the same time the label was made. There is usually a dull area on the label where the date is to be stamped as well. Look for it. If it passes all of these tests, it is probably real. There are good counterfeits that will pass all these tests though, so keep that in mind. Just use your head and you should be fine most of the time. Stacking Info: Deca-Durabolin is the “jack of all trades” when it comes to steroids. This is “the steroid” to stack with others. I am convinced that using deca with other drugs is where the term “stacking” originally came from. Deca is typically stacked with many things like dianabol, any of the various testosterones, sostanon 250, anadrol 50, etc, etc for adding large amounts of muscle mass. It can be taken along with anavar, masteron, parabolan, primobolan, etc. if you are looking to add better quality muscle that will stay with you longer and make you look harder since you will have less of the water retention associated with the dbols and testosterones.

DEPO TESTOSTERONE

DEPO TESTOSTERONE 200mg/ml: R380.00/10ml vial

Depo-testosterone is the brand name for testosterone cypionate by Upjohn. Depo-testosterone is a moderately powerful androgen. Athletes report it to be somewhat effective in promoting gains in strength and muscle mass. The drawbacks of this steroid, however, outweigh the benefits. Its reports side-effects includinggynecomastia, testicular dysfunction, severe acne. decreased libido, and chronic priapism.

DEPOTRONE

DEPOTRONE 200mg/2ml ampule: R260.00/10 amps

Description: 200 mgs. / 2ml vials. This is highly anabolic and androgenic and aromatizes easily like Anadrol. Users of this drug usually have big strength and size gains. It is moderately toxic to the liver. At higher doses all of the bad side effects are shown such as water retention, baldness, acne, aggressive behavior, etc. Active in your body for about 7 days at a time.
Effective Dose: 200 - 600 mgs. / week • Street Price: R260.00/10 x 2ml ampules 200mg/amp.
Stacking Info: Regularly stacked with just about everything

DIANABOL

DIANABOL 5mg/tab: R270.00/100 tabs R1600/1000 tabs

5 mg tablets. Dianabol is still one of the most effective strength and size building oral steroid. It is sometimes rather costly. It causes considerable water retention and aromatizes quite a bit so you`ll see quite a bit of dosage jumps while using it. Available over the counter in Mexico with no prescription needed. People get good results with Dianabol. Dianabol is now available under its generic name of Methandrostenelone and is being produced domestically by Rubu Labs. Originally, Dianabol came in 50 mgs tablets. It was developed in the mid-forties and experimentally used on returning prisoners of war that had been on very low food intakes. Actual dosages of the generally available 5 mg (it also comes in 2,5 mgs tablets) many doctors prescribe a 4 day with 8 to 10 the average for self-made expert and 100 is not unheard of
in one day. The generic version may be the best price if Anadrol keeps rising in price. Not many women use it because it is high in androgens. Some people report sleeplessness with high dosages.
Methandrostenolone was a very popular drug in the 70´s, and still is. It is a 17 alpha-alkyl based steroid which produces dramatic strength and size gains. This is also a very toxic drug. This drug is probably the reason for Arnold’s muscles. Arnold loved a combination of Primobolan Depot and Dianabol. Dosages: 15-35mg per day

FERTOMID

FERTOMID-25mg:R230.00
See clomid.

Human Growth hormone

HUMAN GROWTH HORMONE.
Nomatropin: R2800.00
Norditropen: R1800.00
The use of exogenous sources of Growth Hormone has been popular in world wide for many years now. Originally, pituitary glands of cadavers. Ascellacrin and Crescormon were the two most popular brand names on this original GH. While production was under way on the synthetic, recombinant DNA versions of this drug, it was discovered that the biologically active form was associated with the formation of a rare brain virus called Creutzveldt Jacob Disease. This was a fatal virus that afflicted a very small number of GH users, none of whom were athletes. In light of this discovery, the FDA removed all of these natural GH versions from the market in the United States. Luckily, the synthetic recombinant versions were approved by the FDA a short time afterwards. These versions were developed after years of experiments with amino acid chains. The first of these versions was patented and produced by Genentech Labs
with the brand name Protropin. A short time later, another form of synthetic growth Hormone gained FDA approval. It was produced by Eli Lilly Labs and brand named Humatrope. This product was allowed to be patented because it was shown to be unique in that it contained a slightly different amino acid chain than the Protropin. The difference was that Humatrope had 191 amino acid chains in sequence and Protropin had 192. For some very complicated reasons, the 191 amino acid configuration has been shown to be more effective. It had been speculated that these synthetic versions of GH would greatly improve the cost effectiveness of using GH, yet that has not been the case. An athlete who wants to do a cycle of GH can still expect to be out as much as $4000 a month. There are numerous versions of Growth Hormone available in Europe, the majority of which are made up of the 191 amino acid sequence. There is even a
form of the original human extract Growth Hormone, called Grorm which is available in a few countries. Although this drug is indicated for the treatment of pituitary deficient dwarfism, it has been used extensively by athletes who are attempting to alter their body composition. Growth Hormone itself, is an endogenous hormone produced by the pituitary gland. It exists at especially high levels during the teen years when it promotes growth of almost all tissues. It also contributes to the deposition of protein and promotes the breakdown of fat for use as energy. As the body reaches full maturation, the endogenous levelsof GH are substantially deminished. After this, GH is still present in the body but at a substantially lower level where it continues to aid in protein synthesis, RNA and DNA reactions and the conversion of body fat to energy. By introducing an exogenous source of this hormone, athletes are hoping to promote these effects, causing the body to deposit more muscle tissue while at the same time reducing body fat stores.
On paper, GH should work exceptionally well; however, it does not seem to be delivering up to its potential. Most athletes who have experimented with this product end up being disappointed. There is some evidence that exogenous sources of GH are being destroyed by antibodies which appear after the introduction of the synthetic compound. Although the 191 amino acid sequence versions have been shown to produce less of an antibody reaction, they are still not yielding consistent results. I have speculated as to whether the introduction of exogenous GH would yield an appreciable degree of efficacy simply due to the fact that the body does not have sufficient receptor affinity to GH in the post-teen years. A number of athletes claim that GH is not that effective on its own, but in a stack with steroids it can do remarkable things. Perhaps there is some type of actual synegism created by the concomitant use of these two agents. Empirical data suggests that the efficacy of GH is dose related and that the majority of users may not have been taking enough of it to get positive results. Despite speculation concerning its efficacy, syntheric GH is being used by thousands of elite athletes. These include men and women bodybuilders, strength athletes, as well as a multitude of Olympic competitors. Although Growth Hormone is banned by athletic committees, there is no method for the detection of it which allows drug tested competitors to use this product freely without any ramifications. Adverse reactions to GH use are rare but technically could involve acromegaly (elongation of the feet, forehead and hands). Other possible side effects involve overgrowth of the elbows or jaw, thickening of the skin and a type of diabetes. There are numerous counterfeit versions of this product which are merely cashing in on the drug’s mystique and high price tag. The legitimate versions must be
refrigerated at all times, before and after they are reconstituted. Effective dosages, seem to be in the area of 2 I.U., 2 - 4 times a week. Cycle length is usually determined by how long the athlete can afford it. Some take the product for 6 week cycles, others use it year round. Legitimate GH is hard to find, when it does show up, it sells for as much as R4000 for 100/I.U.

HELOTESTIN

HELOTESTIN: R1050.00/50 tabs R1900.00/100 tabs

10 mg/tab. 100/bottle by Upjohn. This is an oral steroid wich is derived from methyltestosterone. Many athletes use this drug to attain strength or a harder look to already lean muscles. The toxicity of this drug is very high. It will not aromatize in dosages of 20 mg per day or less. Aggressiveness is often increased in men who are on Halotestin. Women avoid the drug of course. If an athelete felt he needed to use Halotestin, it should not be taken for more than four weeks at a time. Dosages of 10 mg to 20 mg daily is though to be ample amount.

KESSAR

KESSAR 20mg:R280.00/pack of 30 tabs
Estrogen receptor antagonists, more simply referred to as anti-estrogens (though this term is often loosely applied to all estrogen maintenance drugs), are drugs that block estrogens from exerting activity in the body. This is actualized by the ability of a particular substance to bind to a segment of the estrogen receptor, yet not activate it. This in turn prevents other estrogens from binding and activating the same receptor site. In a clinical setting an estrogen antagonist, most prominently the drug tamoxifen citrate (sold under the brand name Nolvadex) is typically used as the first line of defense during advanced breast cancer therapy. Its use can efficiently deprive estrogen responsive cancer cells of necessary hormone, allowing a high rate of response in patients with such forms of cancer. Stronger agents such as aromatase inhibitors (discussed below) are usually a second choice, substituted when conventional antiestrogen therapy fails to elicit the desired response. A drug like tamoxifen is preferred over other agents as the first course of breast cancer treatment for a number of reasons, most due to the fact that that it is
both extremely effective yet does not inhibit the actual formation of estrogen in the body. Among other things, this may allow Nolvadex therapy to be somewhat more comfortable for the patient. Although many women (particularly pre-menopausal) seem to suffer menopausal-like side effects with virtually all estrogen maintenance drugs, estrogen antagonists are often somewhat more tolerable than agents that block the synthesis of estrogen. In fact the activity of tamoxifen is itself variable, such that in certain target tissues it may actually act as an agonist (activator) of the estrogen receptor. It therefore does not completely diminish the biological activity of estrogens, though it does considerably reduce it nonetheless. It is also well understood in medicine today that estrogens play a supportive role in the cardiovascular system. For example, studies show that a rise in the estrogen level (as in post-menopausal estrogen replacement therapy) is typically linked with a reduction in LDL (bad) cholesterol, and a rise in HDL (good) cholesterol. The ability of tamoxifen to act as an estrogen agonist in the liver likewise gives it what may be its most welcome property, namely that it exhibits an estrogenic, rather than antiestrogenic, effect on blood lipid (cholesterol) values. As a 1998 study by the Department of Clinical Oncology in the Netherlands Cancer Institute shows, during long-term treatment with tamoxifen (6 months) a lowered LDL cholesterol level, and significantly elevated HDL cholesterol level and HDL-C/total-cholesterol ratio may result. This trend should reduce an important risk factor for heart disease, obviously a welcome effect during treatment. For the steroid-using athlete already faced with negative alterations in lipid profiles, such an effect could obviously an important consideration. Clomid (clomiphene citrate) is very similar in structure to Nolvadex, both drugs being classified as triphenylethylene compounds and used clinically for similar
purposes (breast cancer as well as female infertility treatment). As well as we see with Nolvadex, Clomid is a partial agonist/antagonist of the estrogen receptor depending on the target tissue in question. Although athletes most commonly think of Clomid as a testosterone-stimulating drug only (another effect of antiestrogenic compounds), to be used at the conclusion of steroid treatment, its activity in the human body is not at all dissimilar to Nolvadex. It should likewise be thought of not as a drug with its own niche of use, but instead as another efficient remedy for gynecomastia similar to Nolvadex (with the related ability to support the release of testosterone). It could clearly replace Nolvadex as a preventative measure against gynecomastia during cycles with aromatizable steroids without noticeably altering the level of effect received, just as Nolvadex can be used effectively to increase the synthesis of testosterone in the body at the conclusion of steroid use (though admittedly Nolvadex may be slightly more potent in both regards)

LAURABOLIN

LAURABOLIN 50mg/ml/10 ml vial: R380.00

Nandrolone Laureate is longer acting form of Deca. The drawback is its poor solubility in oil. Deca durabolin can be consentrated as high as 200mg/cc. Laurabolins limit is 50mg/cc. Because of its long acting properties its also very slow acting. Almost as effective as Deca if you are not impatient for results.It comes in 50mg/ml 10ml vials.

Size:***
Strenght:***
Side effects:**
Dose: 200-800mg every 14-20 days
MELANOTAN II(Melatonin): R950.00/2ml vial.
In the world of bodybuilding and vanity, mainly used to darken skin pigmentation.
If not only for darker skin, then why:
Melatonin. The focus of a media blitz from Good Morning America to Newsweek magazine to articles in our daily newspapers, and even 90 Minutes. Books and articles on the subject explode onto the scene almost weekly. Just what's all the hype about?Cellular biologist Dr. Russell J. Reiter of the University of Texas Health Science Center in San Antonio, Texas, can tell you. He has been researching melatonin for thirty years. His studies have led him to the conclusion that melatonin stands as the most powerful antioxidant molecule to be discovered yet a hormone that can preset the body's aging clock, turning back the ravages of time.(1) Scientitsts may be on the verge of discovering the real "Fountain of Youth" that Ponce de Leon only dreamed about.The way it's being talked about, melatonin sounds like the "medical miracle" of the century. Judging by research findings on this hormone of the pineal gland, it just may be. Benefits range from its use as a gentle, effective sleeping aid to future birth control pills with no adverse side effects.(1) That is more than can be said about any medication.
The Pineal Gland & Melatonin:
Scientists once thought of the pineal gland as the "appendix of the brain," having little use in the neuroendocrine system. Then in the 1960s and 1970s, scientists such as Dr. Reiter began to unravel its mystery as the "biological clock" of the body.(2)The Hindus referred to the pineal gland as the body's "third eye." Interestingly, it is a light-sensitive vestigial remnant of what actually was a third eye in lower animals.(3,4) Situated deep within the brain and connected by a direct pathway to the eyes, the pea-sized pineal gland controls our sleep/wake cycle, which scientists refer to as circadian rhythm.(4) It secretes almost undetectable amounts of the hormone melatonin in response to periods of light and darkness. The pineal gland produces melatonin only during darkness, while production is suppressed by bright light.(2,3,5)Melatonin establishes the biological rhythm of every cell in the body. The presence of adequate amounts of melatonin induces sleep and may reduce anxiety, panic disorders and migraines.(5) Interruption of routine, such as shift work, jet lag, or even an erratic daily schedule can reduce Melatonin levels and de-synchronize the body's internal biological clock.Melatonin production rises sharply from almost nothing at birth and peaks in late childhood, falling dramatically just before puberty and declining more gradually into old age.(6) This accounts for the increased incidence of insomnia among the elderly. Today, melatonin ranks as one of the most important hormones, possibly even the "master hormone" stimulating the release of a wide variety of other hormones from the pituitary gland.(2,4)
Free Radical Fighter:
Researchers have discovered melatonin to have the most powerful antioxidant properties of any free-radical fighter. Cellular oxidative damage by free radicals has been linked to formation of cataracts as well as other degenerative conditions.(4,7,8) Melatonin scavenges and neutralizes the most damaging free redical, the hydroxyl radical, five times better than gluathione, and is twice as effective in deactivating the peroxyl radical as vitamin E. It also stimulates glutathione peroxidase activity and inhibits nitric oxide synthase, thereby reducing the production of the highly toxic hydroxyl and nitric oxide free radicals.(7) These findings point to the anti-aging role of melatonin and its relationship to prevention of age-related diseases such as Alzheimer's, cancer, and heart disease.
Immune Enhancer:
Melatonin also boosts immune function through both its antioxidant action and its relationship with the thymus gland.(4) When melatonin was added to the night-time drinking water of older mice, it not only significantly extended their life span, but also kept them disease-free by improving their immune response. Melatonin increased thymus size and cellular activity, strengthening the immune system.(4) Other studies have demonstrated melatonin's immune-enhancing ability in strengthening antibody response, knocking out viruses, moderating the effects of corticosteroid overproduction in response to stress, and rejuvenating thyroid function which influences T-cell production. Transplanting pineal glands from young to older mice also restored youthful zinc levels which are essential for immune function.(4)
Melatonin/Cancer Connection:
Recent research has shown that melatonin may have a powerful effect on protection against and treatment of cancer, including breast, cervical and prostate cancers.(11,12) Low melatonin levels seem to parallel cancer growth.(2,4,13) Melatonin is a potent oncostatic agent, preventing both the initiation and promotion of cancer.(14) Exposure to electromagnetic fields has been shown to increase the risk of breast cancer, not directly but as a result of suppressing the nocturnal rise in melatonin levels.(4) Melatonin (10 mg./night) has also been proven to amplify the immune effects of interleukin 2 (IL-2) treatment for cancer and to significantly reduce its toxicity and side effects.(4, 15)
Melatonin & S.A.D:
Patients with Seasonal Affective Disorder (SAD) have an abnormal seasonal variation and suppression of melatonin by light.(15) During winter, the decreased duration of daylight somehow alters the circannual rhythm of SAD patients. Light therapy and melatonin supplementation have proved beneficial in many cases.(4)

MASTERON

MASTERON: R850.00
Masteron, or drostanolone propionate, is a popular steroid among competitive bodybuilders. It is commonly used in contest preparation for many reasons. To begin with, drostanolone propionate is a derivative of DHT(dihydrotestosterone), and therefore, it will not aromatize into estrogen. Competing bodybuilders find this extremely beneficial because aromatization typically causes excess water retention which may give the muscles a smooth appearance. Another advantage
of Masteron is its strong androgenic component. The androgenic effect of this steroid can cause a noticeable improvement in muscle density and hardness which can help the bodybuilder obtain the “ripped” look if his bodyfat percentage is low enough. The androgenic effect is also crucial because it helps to provide sufficent “kick” or “drive” for intense training when an athlete has lowered his caloric intake for contest preparation. Masteron can also be used successfully
by bodybuilders preparing for a drug-tested show. The substance drostanolone propionate is fast acting and quickly broken down. The athlete can therefore use Masteron up to about ten days before a drug test. The average dosage of Masteron is 100 mg injected every other day. It is best to inject Masteron every 2-3 days because it has a short duration of effect. Popular steroids stacked with Masteron include Parabolan(trenbolone hexahydrobencylcarbonate), Winstrol(stanozolol), and oxandrolone. Athletes rarely experience any side effects with this steroid. Masteron is not hepatoxic, and gynecomastia should not be a concern since it does not convert into estrogen. Some possible side effects include acne, accelerated hair loss, and increased aggression. The main disadvantage of Masteron is its very poor availability on the black market and its high price. Masteron from Nomad labs comes in 10ml vials. Each 1 ml will contain 100 mg of drostanolone propionate. One of these vials containing 10ml will cost more or less R850.00.

NOMASUST

NOMASUST: R550.00/10ml vial

This is a blend of four different steroids:
Testosterone propionate: 30mg stays active for 3-4 days
Testosterone Phenylpropionate: 60mg -”- 1-3 weeks
Testosterone Isocaporate: 60mg -”- 1-3 weeks
Testosterone decanotate: 100mg -”- 2-4 weeks
This is a self tapering steroid blend which gives good gains. Will give good results when used in a decrease the days cycle.
Size:****
Strengh:****
Side effects:****
Dose: 1-4cc per week

NOMAVIRON

NOMAVIRON 300/250mg test enanthate/50mg test propionate. R550.00
Testosterone enanthate.
Testosterone enanthate is currently the most popular ester of testosterone available to athletes. Unlike cypionate, enanthate is manufactured by various companies all over the world. Ampules of Testoviron from Schering are probably the most popular although many others exist. Enanthate is a long acting testosterone similar to cypionate. Injections are taken once weekly, with a dosage of 200mg - 600mg per week.
Testosterone propionate.
This is a fast acting oil based testosterone. It is very similar to cypionate except it is only effective in the system for about 5 days; therefore, shots are required twice a week. Propionate can be effective for size and strength gains like other testosterones and it has been associated with the usual testosterone side effects like: gynecomastia, water retention and aggression. Testosterone propionate is having somewhat of a comeback recently as it is one of the few drugs that are still manufactured in the United States. Average dosages are in the range of 200-400mg per week.

PREGNAL.

PREGNAL(HCG):1500 iu/R400.00, 5000 iu/R550.00

Pregnyl by Organon. 1500 to 5000 IU (International Units) per 1ml amuple. This drug is not a steroid but it is widely used in athletics today. HCG is a natural protein hormone secreted by the human placenta and purified from the urine of pregnant women. This hormone is not a male hormone but mimics the natural hormone LH (Luteinizing Hormone) almost identically. LH stimulates the production of testosterone by the testis in males. HCG sends the same message and results in increased testosterone production by stimulating the leydig cells of the testis. HCG is used to treat women with certain ovarian disorders and it is used to stimulate the testes in hypogonadal men. Athletes use HCG to increase the body’s own natural production of testosterone which is often depressed by long term steroid use. When steroids are used in
high dosages, they can cause a false signal to go to the hypothalamus that results in a depressed signal to the testicles. Over a period of weeks, this depressed signal causes the testicles to atrophy. To avoid this, athletes will use HCG to keep an artificial signal going to the testis.
When administered, HCG raises serum testosterone very quickly. A rise in testosterone first appears about 2 hours after injecting HCG. The second peak occurs about 2 to 4 days later. HCG therapy has been found to be very effective in the prevention of testicular atrophy as well as to use the body’s own biochemical stimulating mechanisms to increase plasma testosterone levels during training. Some steroid users find that they have some of their best strength and size gains
while using HCG in conjunction with steroids. This may well be due to the fact that the body has a high level of natural androgens as well as the artificial steroid hormones at that time. The optimal dosage for an athlete using HCG has never been established, but it is thought that a single shot of 1500 IU per week will get the desired results. Cycles on HCG should be kept down to around 3 weeks at a time with an off cycle of at least a month in between. For example, one might use the HCG for 2 or 3 weeks in the middle of a cycle, and for 2 or 3 weeks at the end of a cycle. It has been speculated that the prolonged use of HCG could repress the body’s own production of gonadotrophins permanently. This is why short cycles are the best way to go. The side effects from HCG use include gynecomastia, water retention, increased sex drive, mood alterations, headaches, and high blood pressure. HCG raises androgen levels in males by up to 400% but it also raises estrogen levels dramatically as well, This is why it can cause gynecomastia. Other side effects seen from HCG use include “morning sickness like” symptoms (nausea and vomiting). There have been no cases of overdose complications with the use of HCG nor have there been any associated carcinomas, liver or renal impairment.

PUMP n POSE "Synthol"

PUMP n POSE (Synthol) R350.00/100ml

Description: Pump n Pose "Synthol" is an intermuscular fatty acid that bodybuilders are now using to give increased size in small muscle groups. Gains of 1 inch in muscles like the calves, biceps, and shoulders are not unheard of. It is actually a synthetic oil that is injected right in to the muscles you want to enhance in size. The way that this product works is that it becomes encapsulated between the fasicles (bundles of muscle fibers). Upon repeated injections, a huge bolus of the oil accumulates, adding volume to the injected muscle. About 30% of the amount injected will be broken down by your enzyme system and is metabolized like a normal fat because of its unique chemical structure. It will not be stored as bodyfat but will be burned very fast as fuel. The remainder of about 70% of the substance will be encapsulated between your muscle fibers and is broken down very slowly over the course of 3 to 5 years. Dan Duchaine recently analyzed a sample of Synthol and found it contained mostly C8 fatty acids, some C10, and about 3% C12 (the C and the number relate to what length the fat is - short, medium, or long). The mixture also contained 7.5% lidocaine (a painkiller) and 7.5% benzyl alcohol. There is currently some debate on whether you can take regular MCT oil as a substitute for “the real Synthol” which costs between $300-400 per bottle. Because of the structure of Synthol and the fast encapsulation your enzyme system, your body has a real hard time spotting the substance and breaking it down. Supposedly if you use this product correctly you won’t come down with any kind of infection or any really bad side effects. To get no detrimental effects you have to be careful about the amounts you inject the first couple of times you use the stuff, otherwise you could experience an accumulation of lymphatic fluids in your arms for a couple of days. Working out while taking Synthol is quite another story. Synthol makes it real hard at first to train because sometimes after just one set of any upper body exercise, your guns will feel pumped like after a hundred sets of any arm exercise. I have not tried this nor Esiclene, but this product is supposedly more painful than esiclene with all of the swelling that you will experience from using this compound. Esiclene was an itallian steroid that was used a lot in the ‘80’s for causing site swelling in order to also bring up laggin bodyparts. Supposedly, not too many people can stand the pain when using Synthol for enlarging the calves, it’s just so nasty. As far as side effects are concerned, that is still up in the air. The makers of the substance say that there are really no side effects but injecting any significant amount of fatty-acid material intramuscularly can be extremely dangerous. When you jab a syringe into a muscle without any knowledge or regard to nerve distribution, you may hit a nerve and possibly cause permanent paralysis of groups of muscle fibers within that area. And besides the increased possibility of developing abscesses, there is also the possibility you might inject the fat into a vein or artery and cause serious tissue damage downstream. If this stuff is accidentally injected into a vein or artery, it could be transported into the lungs, possibly causing a “pulmonary embolism” or perhaps even into the brain, causing a “cardioembolic stroke” or death. It’s also known that injecting fatty acids into the system can lead to a condition where blood clots can develop, resulting in coronaries and strokes.” The bottom line is that you need to weigh the risks to benefits ratio for yourself and decide if it is worth it for you to get some instant gains. In my opinion, this would be an excellent precontest drug but for the average bodybuilder that will never compete it really is not worth the pain or cost to use. I have not used this compound and probably never will. It is just another of those things that competitive bodybuilders use to give them an edge over the competition.
Effective Dose:
Start with 1ML, deep into the muscle with a 1/4 inch needle. Be sure to use sterile technique at all times. Continue at this rate for ten days. Then increase to 2ML a day for ten days. Now 3ML a day until the muscle gain stops. Now return to 1ML a day for 30 days. Now 1ML twice a week for four weeks. Now 1ML once a week for four weeks. The gains are now said to be permanent... Arms will be a good 2 inches up after three weeks and hold. After a four month break a further gain can be made by repeating the cycle.
ALWAYS DRAW BACK BEFORE DELIVERY, IF THE SYRINGE FILLS WITH BLOOD ABORT THE ATTEMPT. FAILURE TO DO SO COULD BE SEVERE. IF IT BLEEDS
AFTER THE INJECTION DO NOT BE ALARMED AS THIS MEANS YOU HAVE PASSED THROUGH A VEIN, BUT NEVER DELIVER INTO ONE.
From what I have observed, the gain are permanent and looks excellent.
Street Price: This product is now available at Noscriptsteroids for R350.00 per bottle. Mesomorphosis is currently one of only two select companies authorized by
Chris Clark of Germany to distribute his original Pump’n Pose Posing Oil in the United States. Don’t settle for ripoff copys of this product. Get the real deal today and watch those arms, shoulders, and all other bodyparts grow now!

PRIMOBOLAN DEPOT

PRIMOBOLAN DEPOT
(methenolone depot)100 mg/cc, or 50 mg/cc 1 cc ampules:
R1100.00/10 ampules
Primobolan Depot is an injectable steroid produced by Schering and sold in various parts of the world. It contains the steroid metenolone enanthate, which is a long acting anabolic with extremely low androgenic properties. The anabolic properties of this steroid also are mild. Primobolan is most commonly used during cutting cycles although some users do stack it with stronger drugs like testosterone and Dianabol for mass cycles. This drug is most commonly injected on a weekly basis and dosages range widely. At 100-200 mg weekly Primobolan should not interfere with natural testosterone levels and should not produce noticeable side effects. In Europe it is not uncommon for Primobolan to be used at such doses for long term therapy. Among athletes, steroid novices will respond to weekly doses of 200 mg but regular users often inject much higher doses looking for a stronger anabolic effect. Primobolan Depot comes in 1ml glass ampules containing 100mg of the drug in Europe and 50mg throughout areas of South America. In the U.S. the 50mg ampules from Mexico and 100mg ampules from Spain most commonly show up.

PROVIRON

PROVIRON: R220.00/10 tabs
email: noscriptsteroids@gmail.com
Proviron, or mesterolone, is a popular antiestrogen used by bodybuilders. It acts as an antiaromatase, which means it prevents the aromatization of steroids into estrogen. Proviron is frequently used by athletes on heavy cycles of steroids to prevent gynecomastia. It is also favored by competitive bodybuilders since a lower estrogen level corresponds with increased muscle hardness and lower water retention.One or two 25 mg per day should be sufficient to prevent gynecomastia. Proviron can also be combined with Nolvadex (tamoxifen citrate) if needed. Side effects are extremely rare with dosages under 100 mg per day. One major problem with Proviron is that it tends to reduce the gains made from a cycle. This is due to the fact that Proviron is an androgen and therefore binds to androgen receptor sites within the body. With Proviron binding to androgen receptor sites, the other steroids present in the body (androgens) are blocked out and unable to take effect. Consequently, many athletes prefer to keep the intake of Proviron at its minimum effective dosage in order to make sufficient gains while still preventing gynecomastia. Proviron is usually fairly easy to obtain on the black market. Most versions are manufactured by Schering and cost about R220.00 for 10 x 25 mg tabs. Proviron can come in push-through strips or small glass vials. There is currently no need to worry about authenticity when buying Proviron since no counterfeits of this product are known exist.

SUSTENON 250

SUSTENON 250. Organon SA: R850.00/6 ampules. Organon Pakinstan R600.00/10 ampules.

Brand Names: Durandron, Sostenon 250, Sustanon, Sustanon 250, Deposterona,
Description: Each sostanon 250 preload contains the following: Testosterone propionate 30 mg, Testosterone phenylpropionate 60 mg, Testosterone isocaproate 60 mg, Testosterone decanoate 100 mg, 250 mgs. / 1 ml ampule.
Sostanon 250 is one of the most popular steroids and for good reason. It is precisely set up to give you results for up to a month after injection because each of the testosterones that make up sostanon 250 stay active in the body for differing time periods. It gives you almost instant
results that you can feel since it will hit you about 3 hours after your first injection. The reason for this is the fast acting properties of the testosterone propionate that is in it. The testosterone phenylpropionate and testosterone isocaproate will typically stay active for about 2-3 weeks each and the testosterone decanoate stays active in the body for up to a month. This combination is what gives sostanon 250 its quick onset which continues to hit you for about 4 weeks after the
last injection. This drug also degrades and tapers nicely for the same reasons. Some people will argue that sostanon is good because since it is made up of multiple types of testosterone, that it “will hit multiple androgen receptors.” This could not be further from the truth. You only have one type of androgen receptor. All steroids hit the same androgen receptor regardless of what you are taking. Sostanon 250 is highly anabolic as well as highly androgenic. This makes it a favorite of those trying to bulk up. It is a steroid that gives you what you are looking for; that 20-25 lbs during a 6 week cycle for most steroid novices. You gain mass rapidly and get a nice kick in stength as well while taking this drug. There is almost a synergistic action to sostanon 250, meaning that the combination of the various testosterones in it work better together than the sum of their parts. In this example, 1+1+1+1=5! Another nice aspect of sostanon 250 is that it aromatizes less and gives you less water retention than other testosterones. This tranlates to a lower risk of gyno and will tend to not give you as much of a “puffy look” as say testosterone cypionate or enanthate would. For these reasons alone, you can see why sostanon 250 would be preferred to other steroids. It is also fairly easy to obtain on the black market and a cinch to buy in Mexico as just about every pharmacy stocks the bodybuilders friend, Sostanon 250!
Side Effects: The side effects tend to resemble other types of testosterones but it tends to not be as harsh. The typical side effects can include the following: nausea, leukopenia, symptoms resembling a peptic ulcer, acne, edema (water retention), excitation or increased aggressiveness (commonly referred to as roid rage), sleeplessness, chills, vomiting, diarrhea, hypertension, prolonged blood clotting time, increase in libido. Females had reported: menstrul irregularities,
post-menopausal bleeding, swelling of the breasts, hoarseness or deepening of the voice, enlargement of the clitoris, and water retention. Men had reported: cases of impotence, chronic priapism, epididymitis, inhibition of testicular function, oligospermia, and bladder irritability. Some people that take sostanon 250 have reported “flu like” symptoms as well. These symptoms include a higher than normal fever, stomach aches, being tired, etc. These side effects tend to go
away after a few days and should not deter you from your goals of gaining muscle mass!
Effective Dose: 250 - 1000 mg / weekly. Sostanon is designed to be a time released steroid though and could theoretically be taken as little as once a month since it stays active in your body for that time period, but for bodybuilding purposes, this is not practical. More commonly, bodybuilders will take between 500 - 750 mg per week for the desired effects. I have heard, and I am saying heard of people taking obscene amounts of sostanon though. I am talking about
3000 mg a week for some of these people. This is of course both stupid and wasteful, but I thought I would fill you in on the extremes. Street Price: R850.00/6 ampules Organon SA or R550.00/10 amps Organon Pakistan. Stacking Info: Very powerful drug which stacks with other steroids very well in a bulking cycle. Sostanon 250 is commonly taken along with anadrol 50, dianabol, deca durabolin if they are looking to “mass up”. You can take with parabolan, winstol, or primobolan if you are looking for more quality muscle gains that would also tend to stay with you longer. It is not typically taken precontest as there is still some water retention associated with taking this drug.
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