Anabolics

The truth of HRT or TRT

Nandrolone Decanoate

Deca Durabolin, which is also known as nandrolone decanoate or sometimes just Deca for short, is perhaps the most recognized type of injectable anabolic steroid next to testosterone itself. Just about every steroid newbie has heard about it, and many of the more experienced steroid users think that it’s an important factor in muscle building. Deca isn’t necessarily unique in its anabolic properties. There are other types of injectable steroids out there which can help produce the same muscle-building results as Deca does. What makes Deca unique, however, is that it has low aromatizing properties. That is to say, it doesn’t convert to estrogen as easily as testosterone does. Another reason for Deca’s popularity is that it also doesn’t produce side effects that are as horrific as those resulting from the use of other steroids. In fact, it even soothes joint pains, which is why some doctors prescribe it for osteoporosis.

Testosterone Enanthate 

It is one of the most popular and commonly used anabolic steroids of all time for the purpose of both performance-enhancing and Testosterone Replacement Therapy (TRT) and in all likelihood, testosterone-Enanthate is the most commonly used testosterone the world over among performance enhancers. Testosterone-Enanthate is one of the most versatile anabolic androgenic steroids one could ever use as it is for all intense purposes the perfect steroid for almost any purpose. Highly anabolic and androgenic in nature, with a rating of 100 in each, as are all testosterone forms, as the demand for this hormone is very high as is the supply you will find Testosterone-Enanthate to be one of the more easily affordable anabolic steroids on the market. From bodybuilders to powerlifters, to on the field athletes and gym rats and everything in-between if you find an individual who has supplemented with anabolic steroids before and in the U.S. you’ll find over six-million who do so simply for cosmetic purposes then you’ll find a strong majority have supplemented with Testosterone-Enanthate.  Prescription medication

Testosterone Propionate

Testosterone propionate was the first to hit the shelves in mass quantity ready for human use. Testosterone propionate is one of the longest existing anabolic steroids and since its inception and into the present day it has remained one of the most popular of all time. Its popularity stems from many points but first and foremost it remains popular because it is simply pure testosterone, a hormone of great anabolic and androgenic power. Further, as we will shortly see testosterone is one of the more versatile hormones we can ever become acquainted with and while all testosterone forms are simply that, testosterone, Testosterone propionate holds a special place in the hearts of many performance enhancers due to its fast-acting nature. Regardless of anything else Testosterone propionate is the easiest testosterone form to control, it is very easy to maintain stable levels, easy to control in-terms of effects and generally one of the more user-friendly anabolic androgenic steroids anyone could ever choose. Thankfully the supply of Testosterone propionate is also through the roof as every underground lab and every steroidal compounding Pharmacy manufactures this testosterone compound making it one of the more readily available and affordable anabolic steroids.

Oxymetholone 

Oxymetholone (Anadrol) is a synthetic anabolic steroid developed by Zoltan ‘Anadrol Z’ F. in 1960. Its primary clinical applications include treatment of osteoporosis and anemia, as well as stimulating muscle growth in undernourished or underdeveloped patients. The drug was approved for human use by the FDA. Later, non-steroidal drugs such as Epogen were developed and proven to be more effective as a treatment for anemia and osteoporosis without the side-effects of oxymetholone. The drug remained available despite this and eventually found a new use in treating HIV wasting syndrome. Presented most commonly as a 50 mg tablet, oxymetholone is the strongest androgenic steroid available. Similarly, it also poses the greatest risk of side effects of any steroid. Despite a very low binding affinity for the androgen receptor, oxymetholone is highly effective in promoting extensive gains in body mass, mostly by greatly improving protein synthesis. For this reason, it is often used by bodybuilders and athletes. Many athletes also use oxymetholone as a method of protection for the joints under heavy loads. Due to the high water retention users experience from this drug, it similarly lubricates the joints and helps protect them from injury. Oxymetholone is widely considered by bodybuilders to have the strongest anabolic effect out of any oral steroid available.

 Trenbolone

There are numerous forms and types of anabolic androgenic steroids and within each one there are often many variations, testosterone being a prime example of a hormone with many faces. Each and every anabolic steroid can serve a primary purpose and will generally carry with it a few secondary qualities and the degree of each just like the steroids themselves can be quite varied. Of all the steroids we can discuss, from mild to strong, powerful and weak you’d be hard-pressed to find a more exciting one than Trenbolone and of the various Trenbolone forms, there is none more exciting than Trenbolone-Acetate. In fact, if we were to label any anabolic androgenic steroid the perfect steroid, side-effects aside it would undoubtedly be Trenbolone-Acetate. trenbolone-Acetate is a very powerful anabolic and androgenic steroidal hormone, so powerful it is 500 times more anabolic than testosterone as well as 500 times more androgenic; with this simple bit of knowledge we could stop right there and that would be enough to give you an understanding of its true power. To understand the hormone a little more clearly we really only need to understand two things; the Trenbolone hormone and how the Acetate ester affects it and by this understanding there will be no doubt, it is the most powerfully amazing steroid of all time.

What is stanozolol?

Stanozolol is a man-made steroid, similar to the naturally occurring steroid testosterone. Stanozolol is used in the treatment of hereditary angioedema, which causes episodes of swelling of the face, extremities, genitals, bowel wall, and throat. Stanozolol may decrease the frequency and severity of these attacks.  Stanozolol may also be used for purposes other than those listed here. What is the most important information I should know about stanozolol?

In rare cases, serious and even fatal cases of liver problems have developed during treatment with stanozolol. Contact your doctor immediately if you experience abdominal pain, light colored stools, dark colored urine, unusual fatigue, nausea or vomiting, or yellowing of the skin or eyes. These may be early signs of liver problems.  Prescription medication $75.00 USD 10ml

What should I discuss with my healthcare provider before taking any kind of steroid?

Do not take anabolic steroids without first talking to your doctor if you have

• prostate cancer;
• breast cancer; or
• a high level of calcium in the blood (hypercalcemia).

Before taking stanozolol, talk to your doctor if you

• have heart or blood vessel disease;
• have had a heart attack;
• have a high level of cholesterol in the blood;
• have bleeding or blood clotting problems;
• have diabetes;
• take an oral anticoagulant (blood thinner);
• have liver problems; or
• have kidney problems.

Clenbuterol, marketed as Dilaterol, Spiropent, Ventipulmin, is a sympathomimetic amine used by sufferers of breathing disorders as a decongestant and bronchodilator. People with chronic breathing disorders such as asthma use this as a bronchodilator to make breathing easier. It is most commonly available as the hydrochloride salt, clenbuterol hydrochloride. Clenbuterol is a β₂ agonist with some structural and pharmacological similarities to epinephrine and salbutamol, but its effects are more potent and longer-lasting as a stimulant and thermogenic drug. It causes an increase in aerobic capacity, central nervous system stimulation, blood pressure, and oxygen transportation. It increases the rate at which body fat is metabolized while increasing the body’s basal metabolic

rate (BMR). It is commonly used for smooth muscle-relaxant properties as a bronchodilator and tocolytic.

Weight-loss drug Although often used by bodybuilders during their “cutting” cycles, the drug has been more recently known to the mainstream, particularly through publicized stories of use by celebrities such as Victoria Beckham, Britney Spears, and Lindsay Lohan,  for its off-label use as a weight-loss drug similar to usage of other sympathomimetic amines such as ephedrine, despite the lack of sufficient clinical testing either supporting or negating such use.

Tamoxifen citrate(estrogen blocker/ gynecomastia) (Nolvadex) is a non-steroidal anti-estrogenic drug. used widely in clinical medicine. it is specifically a Selective Estrogen-Receptor Modulator (SERM) of the triphenylethylene family and possesses both estrogen agonist and antagonist properties.As such, it may act as an estrogen in some tissues while blocking the action of estrogen in others. ln breast tissue tamoxifen citrate is a strong anti-estrogen, and as a result, it is commonly used in the treatment of hormone-responsive breast cancer in women.is a non-steroidal anti-estrogenic drug. used widely in clinical medicine. it is specifically a Selective Estrogen-Receptor Modulator (SERM) of the triphenylethylene family and possesses both estrogen agonist and antagonist properties.As such, it may act as an estrogen in some tissues while blocking the action of estrogen in others. in breast tissue tamoxifen citrate is a strong anti-estrogen, and as a result, it is commonly used in the treatment of hormone-responsive breast cancer in women. in some cases it is even utilized as a preventative measure, taken by women with an extremely

the high familial tendency for breast cancer. in male bodybuilders and athletes, tamoxifen citrate is commonly used (off-label) to counter the side effects caused by elevated estrogens subsequent to the use of certain anabolic/androgenic steroids. The primary worry among the athlete/bodybuilding population is gynecomastia or the very unsightly development of female breast tissue in men.This can be first noticed by the appearance of swelling or a small lump under the nipple. if left to progress, this can develop into a large hard-tissue gynecomastia that may be an irreversible occurrence without surgery. The estrogen can also lead to an increase in the level of water retained in the body, resulting in a notable loss of definition as the muscles begin to look smooth (even bloated) due to the retention of subcutaneous fluid. Fat storage may also be life eased as estrogen levels rise in men. ln fact, differences in the estrogen/androgen ratio are one of the reasons women have 3 higher body fat percentage, and different fat distribution (hips/thighs), than men.

Arimidex (Anastrozole) (anti estrogen aromatase/gynecomastia)Anastrozole is a powerful anti-estrogen medication commonly sold under the brand name “Arimidex” and it is by that name most are familiar with the compound. As an anti-estrogen medication, Arimidex belongs to the aromatase inhibitor (AI) family and it is by this designation we truly see the function of this medication. First brought to the market by AstraZeneca, Arimidex was created in an effort to combat breast cancer in post-menopausal women. As we are aware estrogen is the enemy when it comes to breast cancer and Arimidex actively reduces the amount the body produces and it is by this trait one can already begin to see how this might be useful in-terms of anabolic steroid use. No, Arimidex is not an anabolic steroid; it is not a steroid in any shape or form but is commonly used in conjunction with anabolic steroids to combat estrogenic related side-effects.

Arimidex: Anastrozole, commonly known as Arimidex is an aromatase inhibitor that actively blocks the aromatase enzyme by-which its duty cannot be performed, that were producing estrogen. By this inhibiting process, the compound can actively reduce estrogen in the body by as much as 80%. Coupled with its estrogen reducing effects Arimidex also greatly increases testosterone in the body and can do so by as much as 50% by increasing total testosterone as well as Luteinizing Hormone (LH) and Follicle Stimulating Hormone (FSH) total output.

Clomid, Clomifene (test PCT, increases natural testosterone production), also known as clomiphene, is a medication used to treat infertility in women who do not ovulate. This includes those who have polycystic ovary syndrome. Use results in a greater chance of twins. It is taken by mouth once a day.Common side effects include pelvic pain and hot flushes. Other side effects can include changes in vision, vomiting, trouble sleeping, ovarian cancer, and seizures. It is not recommended in people with liver disease or who are pregnant. Clomifene is in the selective estrogen receptor modulator (SERM) family of medication. It works by causing the release of gonadotrophin by the hypothalamus. 

Clomifene was approved for medical use in the United States in 1967.  It is on the World Health Organization’s List of Essential Medicines, the most effective and safe medicines needed in a health system.  It is available as a generic medication. The wholesale cost in the developing world is about 0.79 to 2.00 USD for a course of treatment. In the United States, the wholesale cost of a course of treatment is 4.80 USD. Its introduction began the era of assisted reproductive technology.

Pramipexole (decreases prolactin/gynecomastia) (Mirapex, Mirapexin, Sifrol) is a dopamine agonist of the non-ergoline class indicated for treating Parkinson’s disease (PD) and restless legs syndrome (RLS). While pramipexole is used clinically (see below), its D₃-preferring receptor binding profile has made it a popular tool compound for preclinical research. For example, pramipexole has been used (in combination with D₂– and or D₃-preferring antagonists) to discover the role of D₃ receptor function in rodent models and tasks for neuropsychiatric disorders.  Of note, it appears that pramipexole, in addition to having effects on dopamine D₃ receptors, may also affect mitochondrial function via a mechanism that remains less understood. A pharmacological approach to separate dopaminergic from non-dopaminergic (e.g. mitochondrial) effects of pramipexole has been to study the effects of the R-stereoisomer of pramipexole (which has a much lower affinity to the dopamine receptors when compared to the S-isomer) side-by-side with the effects of the S-isomer.

Finasteride,(removes DHT, prevents hair loss) sold under the brand names Proscar and Propecia among others, is a medication used for the treatment of benign prostatic hyperplasia (enlarged prostate) and male pattern hair loss. It is a type II and type III 5α-reductase inhibitor;  5α-reductase, an enzyme, converts testosterone to dihydrotestosterone (DHT).

Finasteride is sometimes used to treat pattern hair loss (androgenetic alopecia) in men only.  Treatment slows further hair loss and provides about 30% improvement in hair loss after six months of treatment, with effectiveness usually only persisting as long as the drug is taken, although on occasion hair loss is slowed indefinitely following withdrawal. Finasteride has also been tested for pattern hair loss in women; the results were no better than placebo.