In January 2003, Hardy briefly turned into a heel (villain) after he attacked Van Dam and Shawn Michaels .    It ended a month later when he saved Stacy Keibler from an attack by then-villain, Christian .  In February, he had a brief program with Michaels, which saw the two team up.   Then, in storyline, Hardy began dating Trish Stratus after saving her from Steven Richards and Victoria in March.  Hardy and Stratus had a brief on-screen relationship that saw the duo talking backstage and teaming together in matches. Hardy competed in his final match (his first departure) against The Rock and lost.   Hardy was released from WWE on April 22, 2003.   The reasons given for the release were Hardy's erratic behavior, drug use, refusal to go to rehab, deteriorating ring performance, as well as constant tardiness and no-showing events.   Hardy also cites "burn out" and the need for time off as reasons for leaving WWE. 
What can I expect from Testosterone Replacement? After your blood test and medical examination, your HRT assessment with our clinic will provide sufficient information to our physician to formulate a customized testosterone replacement program for you. Unlike testosterone and steroid sellers you find online, our licensed hormone physicians have in-depth experience and training from Cenegenics®, Mayo Clinic and Cleveland Clinics. You will receive personalized service and attention as well as close monitoring of your TRT program. If HGH, thyroid, DHEA, progesterone or estrogen therapy is required our experienced physician will make sure your receive the most comprehensive treatment available in either local clinics or online. Most men feel a dramatic increase in sex drive, increased energy and drive within the first 30 days of low t treatment. When combined with HCG and HGH injections, even better results are achieved and within six months to a year dramatic results are clearly visible. Patients usually look better and feel better, more fit and trim, more youthful and vital.
Corticosteroids have been used as drug treatment for some time. Lewis Sarett of Merck & Co. was the first to synthesize cortisone, using a complicated 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.