Hello everyone I was looking to see if there was some peptide protocols, or over the counter supplements to rebuild Bdnf, neuroplasticity, memory, and oxidative stress from being on adderall for a long time prescribed.

Most people focus on training their bodies but rarely put the same discipline into training their brains. Yet the brain works like a muscle—it responds best when challenged, stressed, and given time to recover. The 30-Day Brain Upgrade is built on that principle. In less than an hour a day, you can rewire your mental routines, sharpen memory, and expand creativity. This first part of the series lays out the weekly structure, the five core pillars, and the first two weeks of practice. The weekly rhythm is simple. Days one through five are work days, focused on thinking routines, reading, and memory practice. Day six is an experiment day, where you apply creative prompts or break patterns. Day seven is integration, where you step back, rest, and reflect. This cycle repeats each week with added complexity so your brain adapts progressively. The five pillars are the scaffolding of the program. The first is high-IQ thinking routines—different mental lenses applied each week: asking five whys, steel-manning the opposite side of an argument, mapping systems, and breaking ideas down to first principles. The second pillar is daily journaling prompts like “What would my life look like if I doubled my learning speed?” or “Which belief of mine might be outdated in five years?” The third pillar is advanced reading, one book per week that challenges and expands your mind. The fourth is memory techniques, beginning with the method of loci and progressing to chunking, dual encoding, and teaching back. The final pillar is strategic rest short daily practices like box breathing or NSDR, a weekly digital fast, and consistent sleep. Week one is about foundations: clarity and focus. You ask “Why is it so?” on daily observations, read chapters from Daniel Kahneman’s Thinking, Fast and Slow, and build your first memory palace. Each day ends with a short rest practice. On day six you do a mental fast, avoiding input for two hours and journaling the ideas that surface. On day seven you unplug for several hours and write a one-page summary of three insights and one action to apply. By the end of the week, you’ve sharpened attention and cleared space for deeper learning.

Everyone wants to crank the GH dial. I get it. But if the “amp” (your terrain) is noisy insulin resistance, chronic inflammation, sluggish thyroid, chaotic sleep you’re just amplifying distortion. The biology is straightforward: outcomes are receptor-limited, terrain-dependent, and circadian-coded. Fix the signal, then turn up the volume. Let’s clear two myths fast so we don’t build on sand. First, BPC-157 has only shown growth-hormone-receptor upregulation in rat tendon cells in a dish. That’s a clue for tendons in vitro, not a green light to claim gut, fat, muscle, or human receptor changes. Second, GH’s fat-loss effect is systemic. Putting shots in the belly doesn’t melt belly fat. In fact, repeating the same injection site can create lipoatrophy. Terrain first. Pulses before pushes. No spot-reduction fairy tales. Here’s an example of framework to think about it. Start by naming the target: are we rebuilding a tendon muscle unit, or are we re-composing body fat and muscle? If both matter, prioritize the injury pain and function come first. With the target set, run a short terrain tune so the GH axis has a clean runway: smooth glucose, lower CRP drivers, verify thyroid adequacy, anchor sleep, and tame free fatty acids with a simple AM walk. Only then choose the tool. If insulin resistance or high cortisol is on the board, favor physiologic pulses with GHRH/GHRP. If someone is lean, euglycemic, low-inflammation, and under clinical supervision, low-dose GH may be considered. Treat BPC-157 as a cytoprotective adjunct with modest expectations; do not assume in-vivo receptor priming. Place timing to respect biology secretagogues early night or right after rehab, GH scheduled to minimize glycemic drag and rotate injection sites. Then measure, learn, and iterate every one to two weeks using signals you actually trust. Use this little map to set your route before touching the throttle: START -> Choose Goal|- A) Injury/Repair`- B) Body Recomp In practice, the injury/repair path looks like this: clear red flags; run the 14-day terrain tune; choose pulses when insulin or stress is the choke point and reserve clinician-supervised GH for lean, low-inflammation cases; keep BPC-157 as an optional adjunct with clear limits; rebuild tissue on the back of training start with pain-gated isometrics, progress to eccentric-dominant work, then tempo/isotonic and energy-system layering; protect sleep; monitor function, pain, ultrasound if available, HRV/sleep, CGM, and common side-effects like edema or paresthesias; adjust with intent.

I would love to hear everyone’s thoughts on preferred method of TRT(exogenous injectable route, or oral route). I am currently on testosterone enthanate 300 a week and primobolan enthanate. I have also tried jatenzo (oral testosterone). I have had great results with that where my free test was higher and total was lower. Also are there any natural ways(supplements, nutrition, and sleep). What peptides help with upping testosterone, and balancing estrogen? I would love to hear all of your opinions and learn something new that I may have missed.

At AlchemIQ Labs, we don’t just follow the science we help write it. While others speculate, we lead with rigorous research, innovative formulations, and uncompromising integrity. Our mission is simple but bold: to redefine what’s possible in cellular medicine and performance by delivering compounds that actually work, not just buzzwords. Every formula we create is grounded in peer-reviewed science. Biogoutide is a first-in-class oral therapy designed to go beyond standard GLP-1 drugs. Where current treatments often sacrifice muscle or cause harsh GI side effects, Bioglutide leverages a quadruple receptor agonist strategy, activating IGF-1, GLP-1, GIP, and glucagon receptors simultaneously. This synergy creates a powerful metabolic reset: GLP-1 + GIP → enhance insulin secretion, improve glucose control, and suppress appetite at the brain level. Glucagon receptor → boosts fat oxidation and raises energy expenditure. IGF-1 receptor → protects and preserves lean muscle mass while fat is being mobilized. Unlike injectables, Bioglutide is orally bioavailable, and is being researched as a once-daily, and able to cross the blood–brain barrier for central appetite modulation. Clinical Proof In Phase 2 clinical trials (13 weeks, 125 participants): Up to 13.8% body weight reduction at the top dose (150 mg/day).No muscle loss observed a key differentiator from GLP-1 monotherapies. Mild side effects only (nausea, diarrhea in <8%), with no severe adverse events. These results position Bioglutide as a superior alternative to single-pathway GLP-1 drugs like semaglutide and tirzepatide, especially for those prioritizing fat loss without compromising muscle integrity. Why It Matters Current GLP-1 agonists are effective but blunt tools—they drive appetite suppression and weight loss but often at the expense of lean tissue and overall metabolic resilience. Bioglutide changes the game by: Targeting multiple pathways at once for balanced, durable results. Preserving muscle through IGF-1 activation while accelerating fat oxidation.