HD

Stenabolic, in current research trials has shown to increases the metabolic activity in skeletal muscle. It has been shown to increases Basal Meabolic Rate (BMR). Stenabolic assists with reducing obesity, and increases muscle strength. Stenabolic has shown to increase endurance Stenabolic SR9009 Discription The half life of Stenabolic is +/- 2 to 4 hours so it is essential to take Stenabolic in 4 – 6 equal doses per day. This will require that you break the tablet in half. Please refer to the packaging on how to break the tablet in half and take as indicated below. Dose range is 20 – 40 mg per day for male athletes and half that for female athletes. Cycle is 8 – 12 weeks. Dosage : Female Athletes 1 – 2 Tablets per day Male Athletes 2 – 4 Tablets per day. Can be stacked with any other SARM

MK-2866 Builds Muscle And Burns Fat With multiple published human trials under its belt, MK-2866 (also called ostarine) is one of the best-studied SARMs. Those studies found powerful results, too. Ostarine shows no meaningful side effects and is very effective at building muscle. Elderly men and women who took modest doses of ostarine for 12 weeks grew 3 pounds of muscle and lost a pound of fat, with no changes to diet or exercise [1]. Cancer patients saw nearly identical results along a similar timeframe [2]. There were no side effects in either study. A pound of muscle a month is about what you would expect with a solid workout routine – but the people taking ostarine in these studies weren’t exercising. Combining the two would be even more powerful, in theory. Pretty impressive.

Andarine is widely considered to be the most potent of all SARMS that help build lean muscle mass. Andarine has been one of the most widely tested and studied of all the SARMS. Tests have proven that Andarine helps retain lean muscle mass as well as enhancing it. However with Andarine this is not the only noted benefit. In addition to strength and lean muscle gains is its powerful fat burning properties as well. Andarine : the all-round super potent SARM for lean hard muscles

Nolvadex is a drug commonly referred to as an anti-estrogen. This would suggest less or no estrogen is produced due to the drug’s actions as in the case of Teslac. Actually, Nolvadex is an estrogen antagonist, meaning it competes with estrogen at estrogen receptor- sites. This prevents the active estrogen from entering its receptor and creating an estrogenic complex capable of activity. Since many AAS aromatize (covert to estrogen) to some degree, the control of feminizing side effects (males should pay attention here) is important. Males normally have a very low estrogen level. During AAS cycles, due to aromatization, estrogen levels rise considerably. This elevated estrogen level can cause feminizing side effects such as increased fat deposits, water retention, and gynecomastia (growth of breast gland tissue and painful tumors under the nipple). As a rule, it is more the ratio of androgens-to-estrogens than the simple increase in estrogen that actually initiates feminizing side effects. It is important that the reader realizes that Nolvadex does not decrease estrogen production and that it simply blocks estrogen receptors. For this reason the sudden discontinuance of Nolvadex will allow the increased level of circulating estrogen to merge with the newly freed receptors and do feminine things to the body. “Enter Proviron”. At the end of a steroid cycle, the body’s natural testosterone production can be impaired. Due to the aromatization of the AAS estrogen levels are significantly higher than normal and Nolvadex only helps by blocking the estrogen receptors. If an athlete abruptly ends an AAS protocol without regeneration of the HPTA under these conditions, much of the hard earned gains would disappear due to estrogen becoming the dominant hormone. So what did the boys (that didn’t want to be a girl) do?

This is a well structured product that acts as a well timed time-released high anabolic/high androgenic testosterone. In fact, due to TESTOSTERONE PROPIONATE, this product becomes active after one day, but through the series of the other 3 testosterones, remains active for 3 weeks. This mixture had a reported better over all effect milligram for milligram than any other testosterone alone. Users experienced a rapid increase in strength and an even increase in solid mass during administration. SUSTANON aromatized less and caused less water retention when compared to other single testosterones and much less than OMNADREN. Liver toxicity was low (Except in ridiculous dosages) as the liver metabolizes testosterone very efficiently. Like all testosterones, SUSTANON provided improved muscle pumps, better post-training recuperation, and an elevation in aggressiveness toward training.

Oxandrolone was often refereed to as an all purpose oral AAS. This drug was once marketed under the product name (still commonly used trade name) of Anavar. It has the unique quality of significantly stimulating (more than other AAS) the synthesis of phosphocreatine in muscle cells which in turn provides faster regeneration of, and a distinct elevation in, ATP. Of course all AAS have this effect to some extent. Oxandrolone is simply unmatched in this aspect. (See Creatine for more info) Due to this quality, a rapid build- up in strength was frequently reported and an obvious distinct hardness in muscle was obtained with little weight gain and no aromatization.