Once the use of Dianabol is complete and all the exogenous steroidal hormones have cleared your system, natural testosterone recovery will begin again. Natural recovery assumes no prior low testosterone condition. It also assumes no damage was done to the Hypothalamic-Pituitary-Testicular-Axis (HPTA) due to improper anabolic steroid use. While natural recovery will begin on its own, it will be slow. For this reason, most are encouraged to implement a Post Cycle Therapy (PCT) plan after anabolic steroid use. Such a plan will commonly include the SERM’s Nolvadex and Clomid, and often additional HCG. This will greatly speed up the recovery process, as well as its overall efficiency. It will not return your natural testosterone levels to normal on its own, if this is something you’ve been told it is a myth. However, it will ensure you have enough testosterone for proper bodily function while your levels continue to naturally rise. Total recovery will still take several months, but this will cut the total time down dramatically and ensure a smooth recovery. Dianabol is a C17-alpha alkylated anabolic steroid, and as a result, carries a hepatotoxic nature. The rate of hepatotoxicity can vary greatly from one C17-aa steroid to the next, and while Dbol is far from the most toxic, we can’t call it mild either. However, its total toxicity should not lead to liver damage if responsible use is followed and the liver was healthy to begin with. During use, liver enzyme values will increase, but it’s important to remember increases in values does not equate to damage but rather stress and potential damage. In order to avoid damage, use should be limited to 6 weeks of total use. There should also be at least 6 weeks of no C17-aa use before beginning a new course. However, most will not begin a new course until their next cycle. In order to provide protection, beyond duration of use recommendations there are several points of consideration. When using a C17-aa steroid like Dianabol, it is extremely important that you avoid excess alcohol consumption, as excess will promote tremendous liver stress, anabolic mass. In fact, avoiding all alcohol isn’t a bad idea. If that’s not appealing, keep in mind alcohol is perhaps the most anti-performance substance we can put in our body, and your total purpose of Dianabol use is performance enhancement. Beyond alcohol, you should also avoid all over the counter (OTC) medications when possible. Many OTC medications carry strong hepatic natures, and in some cases, far more pronounced than many anabolic steroids. Use should be limited to when only absolutely necessary. Once all C17-aa steroid use has come to an end, liver detoxifiers supplements are also recommended.
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It is also appealing to athletes, who do not want to be carrying additional water weight when performing. Women can typically experience better muscle gains compared to men on anavar , even with a modest dose of 5-10mg per day. Anavar has a significant impact on strength, which is surprising to some considering it is deemed a ‘cutting steroid’, and doesn’t cause dramatic muscle/weight gain. Anavar’s ability to rapidly increase strength is mainly due to it being exogenous testosterone, however it also has a dramatic effect on ATP (Adenosine triphosphate) production and creatine content inside the muscle cells. Higher levels of ATP is beneficial for those who want to hit new PR’s when bulking, anabolic mass. Or for users cutting, who may otherwise lose strength whilst eating low calories for a prolonged period of time. Users have reported anavar significantly increasing strength gains, despite eating low calories. This is also why powerlifters may take anavar before a competition, if they want a boost in strength (without much weight gain). Dr Thomas O’Connor states that top elite powerlifters in the 1970’s, whom he has treated, were all on anavar. Thus, the connotation of it being a ‘girl steroid’ isn’t quite the case, with some of the strongest men in the world taking it too (8). Anavar is one of the best steroids on the market, in regards to side effects. Research has shown it to have ‘excellent safety’ in long-term medical settings (9). Due to its mild nature, it is commonly used by beginner bodybuilders looking to build modest amounts of muscle and fat. A general rule with steroids is : the better the results, the more side effects. Anavar’s benefits aren’t overly powerful (at least compared to other steroids), but the side effects are very tolerable. Its risk/reward ratio is thus very positive. Anavar is a c17-alpha alkylated oral steroid, which is beneficial, as the compound will be fully active after bypassing the liver. However, unlike other oral steroids, anavar’s not significantly hepatotoxic. This is due to anavar being metabolised mainly by the kidneys, instead of the liver. Some of the anavar will bypass through the liver, however this is a smaller percentage compared to other C17-aa steroids. Research shows that 20mg of oxandrolone causes 72% less BSP ( Sulfobromophthalein; a marker of liver stress), compared to an equal dose of f luoxymesterone (10). Fluoxymesterone is also a C17-aa steroid. Thus liver enzymes (AST/ALT) are likely to rise on anavar, however this will only be a mild increase, compared to oral dianabol or anadrol for example. Research shows that elevated enzymes are likely to return to normal, after discontinuing oxandrolone (11). 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