Hello Everyone;
Hope everyone is doing well !

Since i got censored (because i talk about one of the taboo molecule, i will do my best to not talk about it just take in consideration that i am Type 1 diabetic since the age of 9 (2008)

Before I begin, I want to make a disclaimer regarding DT1 molecule. It goes without saying that I do not encourage anyone to take "taboo molecule" given the risk-benefit ratio. It is a very situational molecule and, if poorly assessed, can be relatively dangerous (hypoglycemic coma, neurological sequelae, or death). For off-label use, do not rely on the bro science associated with these effects, as you risk being proportionally disappointed.
When you have Type 1 Diabetes (T1D), this disease, unlike other variants (T2D, etc.), is not directly related to family history or a poor hormonal profile. It is more or less random, an irreversible autoimmune disease (for now) that destroys the pancreatic cells that naturally produce "taboo molecule". It’s like if one day your testosterone production suddenly and irreversibly stops. Once declared, it manifests through a ketoacidosis crisis which induces (if not detected quickly) a metabolism (ketogenesis) that consumes fat.. Without "Taboo molecule" your body is unable to assimilate glucose, so it consumes your fats until a critical threshold where you become dehydrated at the cellular level, fall into a coma, and die. In my case, I was taken care in an accute state of anorexia (20 kg / 44 lbs, the weight of an empty barbell).
I got a protocol of fast-acting "taboo molecule" and long-acting "taboo molecule" designed to mimic the natural secretion of "taboo molecule" in an well being human. (Think of it as TRT but for the pancreas). The pancreas (when functioning properly) continuously micro-adjusts the "taboo molecule" levels to counterbalance the free glucose in the blood, and during significant intake, it creates a proportional peak. In this case, the basal "taboo molecule" smooths out the natural micro-adjustments (physiological needs) of the pancreas, which is an 'average' of the needs between meals, and the bolus simulates a blood sugar spike. In practice, it's more complicated than that, but it would involve discussing dosage (fobbiden on public forum).

The only essential information to retain regarding Type 1 Diabetes (T1D) is that overall needs are proportional to the individual's basal metabolism, just that the adjustments are made exogenously (like TRT). The advantages are the predictability of blood sugar spikes for meals and a slight anabolic effect. The constraints include increased sensitivity/resistance to this molecule. Necessary adjustments must be made to correlate with anabolic product profiles. It's not binary; there are 'safety' measures to take regarding dosage. But once found, as long as the protocol remains simple (similar product lifespans), it can be managed effectively.

From 2018 to 2021, I competed at a national level in powerlifting (at a weight of 80.9 kg / 178,3 lbs during weigh-ins). Outside of competition, I fluctuated between 84 (185 lbs) and 86 kg (189,5 lbs), with an intake of 3200-3500 kcal/day (fluctuation mainly because of glycogen, primarily water retention) At that time, Covid forced my hand a bit to simply stop my progression, and I abandoned the lifestyle that went with it for professional reasons. My weight hasn't changed much honestly (given the abrupt stop), and currently, I have been stabilized at 76 kg (165,5 lbs) with a diet of 2000 kcal/day (with a variation of +/- 400 kcal). Having now different goals, I plan to achieve the following protocol once I have sufficiently lowered my BF (14% atm for a set until december 2024 of 12%, considering to minimize certain side effects (aromatase).

In December 2024, I will undergo a week of "taboo molecule" therapy to determine the exact sensitivity ratios to this molecule, which, like aromatization, varies from one individual to another. I will apply a safety margin (0.75 of the reference dose and progressive increments based on basal metabolism (glycogenesis), which will likely increase and therefore lower blood sugar, then increment based on controls).

The protocol will start in January 2025, i will go for 10 weeks of cycle. (see the table)

(Given that my goal is purely to aim for lean mass with strength gains and general abilities allowing me to handle 3 sessions of (S/B/D and variants), 2 supplementary sessions (specific strengthening), and 2 Kickboxing sessions per week. I do not wish to exceed 83 kg / 182.9 lbs (variable reference could be more could be less) with a low body fat percentage (no fixed reference but below 9-8% if that seems realistic) and will try to aim to maintain 2 cyle a year depending on how much i loose the gain afterall.

Looking forward to your feedback, especially from the most experienced users (and T1Ds who might have similar experiences). Wishing you a pleasant day!"