* Testosterone-Propionate is optimal but Testosterone-Cypionate or Testosterone-Enanthate can be used if the Propionate is a problem for you.
* Trenbolone-Acetate will really set this cycle off more so than any steroid in the stack. If you respond poorly to the hormone you might replace it with Masteron-Propionate at a dosing of 300mg per week; three injections of 100mg each.
* While Equipoise on its own is not a great mass builder, coupled with Testosterone-Propionate and the initial Dianabol use you will produce some very solid gains and see your strength increase very nicely. Further, EQ will promote a more conditioned look while you’re still growing.
* Arimidex may not be needed for some but most will be best served with this low dose. If aromatase related side-effects become a problem you will need to increase the dose to 1mg/eod and in most all men this will eliminate the problems.
* How much weight can you gain from this cycle? That’s a hard question to answer; it will greatly depend on how high your calorie intake is. If you are eating a maintenance level diet you may be able to put on 7-10lbs of tissue, this is excluding any water weight that might come with the Dianabol but any water weight will dissipate shortly after it’s discontinued. Further, the Arimidex will greatly help control this issue. Moreover, the higher your carb intake is above necessity the more water you’ll probably hold.
Lewis Sarett of Merck & Co. was the first to synthesize cortisone, using a 36-step process that started with deoxycholic acid, which was extracted from ox bile .  The low efficiency of converting deoxycholic acid into cortisone led to a cost of US $200 per gram. Russell Marker , at Syntex , discovered a much cheaper and more convenient starting material, diosgenin from wild Mexican yams . His conversion of diosgenin into progesterone by a four-step process now known as Marker degradation was an important step in mass production of all steroidal hormones, including cortisone and chemicals used in hormonal contraception .  In 1952, . Peterson and . Murray of Upjohn developed a process that used Rhizopus mold to oxidize progesterone into a compound that was readily converted to cortisone.  The ability to cheaply synthesize large quantities of cortisone from the diosgenin in yams resulted in a rapid drop in price to US $6 per gram, falling to $ per gram by 1980. Percy Julian's research also aided progress in the field.  The exact nature of cortisone's anti-inflammatory action remained a mystery for years after, however, until the leukocyte adhesion cascade and the role of phospholipase A2 in the production of prostaglandins and leukotrienes was fully understood in the early 1980s.