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Leo Rebel🇻🇦

Leo Rebel🇻🇦

@Ghey724712

ex Protestant. 161 IQ. Here to do the Lord’s work and spread the truth. Get your testosterone checked before you start arguments online.

United States Katılım Haziran 2025
87 Takip Edilen121 Takipçiler
JoMir
JoMir@theAceUrok·
@Ghey724712 @newstart_2024 Shit I love gay men… I’d fuqqin encourage the shit if I was like u .. white and ugly.. except I’m not.. I’m black and beautiful… and I have been getting girls to come play with me since I was like 4 yo.. the hard part is getting them to leave me tf alone #lol
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Camus
Camus@newstart_2024·
Gay men often have a more “hyper male” finger ratio. Andrew Huberman explained the science: pointer vs ring finger length is linked to testosterone exposure in the womb. Lesbians tend to show a pattern similar to heterosexual men. The more older brothers a guy has, the higher the chance he’ll be gay, due to increased testosterone in utero. These differences appear at birth, showing strong biological roots. What do you think about the role of biology in sexual orientation?
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💯🧬 Jake 🧬💯
💯🧬 Jake 🧬💯@BiohackerJake·
💪My experience with HGH (solo) so far. 💪 After several months running HGH daily (AM fasted), I wanted to actually talk about what the addition has been like in real life — not the hype, not the bro-science extremes, just how it’s played out so far. I’m currently running an experiment layering Tesamorelin at night on top of the HGH AM protocol, and that’s going to stay my setup for the foreseeable future. But this post is purely about the HGH piece. HGH is a long-game compound. I knew that going in. You don’t wake up in week three looking like a different person. The changes come in layers over weeks and months — subtle at first, then you look back and realize the cumulative effect is bigger than you thought. That matches what I’ve experienced. First thing worth clarifying: this isn’t TRT. There’s no nightmare shutdown scenario where you have to worry about restarting natural production like you do with exogenous testosterone. Exogenous HGH suppresses your own GH output through negative feedback, but once you stop, endogenous production generally recovers relatively quickly — often within days to a couple of weeks depending on dose and how long you ran it. That’s a big practical difference for a lot of guys. I already had solid IGF-1 levels before starting. I wasn’t chasing numbers on paper. My goal was very specific: increase basal metabolic rate and fat oxidation (especially in the fasted state) while keeping everything healthy long-term. The vision is being able to eventually eat at a higher calorie maintenance, hold more muscle and size, and still stay lean with flexibility. Compounds like Retatrutide have made that body comp flexibility more realistic for a lot of us. So why not stack one of the most well-researched longevity and lipolytic compounds on top of it? HGH is one of the strongest drivers of lipolysis we have access to, particularly in the fasted state. It increases free fatty acid release and shifts fuel utilization toward fat burning. Pair that with the healing, collagen, recovery, and overall tissue quality benefits, and it made sense to add it to the stack instead of just running more fat-loss agents. Early on (first few weeks), the most noticeable things were slight water retention and better sleep quality. The water retention is pretty common — HGH promotes sodium retention and increases extracellular fluid volume. For me it wasn’t dramatic, but it was there. Sleep felt deeper and more restorative, though I’ll be honest — I still manage to blunt a lot of that with the daily stimulant load I run. Even with that, I noticed the same “function on less sleep” effect that a lot of guys get on TRT. It’s not ideal long-term, but it’s a real perk when training volume is high. As time went on, the water retention settled into more of a “massing out” look rather than just bloating. It’s not new muscle or strength per se — it’s the way the fluid distributes. Shoulders, chest, and arms fill out a tee-shirt better. Sometimes the lower abs look a little softer from it, but overall the visual is usually positive. That “full but not sloppy” look is pretty common once you’re past the initial phase. The biggest practical win so far has been recovery. Daily heavy dumbbell training + 90 minutes of incline walking is a lot of volume. Before HGH I was feeling the cumulative fatigue more. Now I genuinely have to program rest days because my body keeps telling me it’s ready to go again. I feel more refreshed between sessions. The tissue repair and collagen synthesis effects are real when you’re beating yourself up every day. I’ve also noticed my hair on the crown seems thicker, but I’m not 100% sure that’s from the HGH (I wear a hat most of the day). Could be, could be coincidence — I’ll keep watching it. At this point I haven’t run into anything that makes me question the commitment. I’ve already stocked up for the long haul and I’m transitioning to slightly higher doses (still capping eventually at 4 IU AM fasted). It has genuinely improved my day-to-day life more than most peptides I’ve run, outside of Retatrutide/Tirzepatide and arguably Tesamorelin during my last cut. I’m looking forward to seeing how body composition continues to shift as the year goes on. I’ve put on noticeable weight in recent months while keeping a lot of the definition and vascularity I was trying to hold onto. Hard to always capture that accurately in photos, but it’s there in the mirror and how clothes fit. I’m still open to experimenting with EOD HGH dosing eventually, but right now I want to finish this Tesamorelin night + HGH AM protocol and see what the endogenous GH pulse + extra visceral fat protection looks like while I’m trying to stay in a surplus. After that I’m planning to bring in IGF-1 LR3 (which works downstream of the GH/IGF-1 axis) while staying on HGH indefinitely and see how that layer feels. Overall it’s been a quiet but meaningful upgrade. Not flashy week-to-week, but the cumulative effect on recovery, body comp flexibility, and just feeling like the machine runs better has been worth it so far.
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drMAWZ
drMAWZ@TheDrMAWZ·
Retatrutide is the most powerful fat-loss compound ever put in humans. It is also a sympathetic-state drug. Elevated resting heart rate, suppressed HRV, blunted morning erections in some users. The fat comes off. The autonomic cost is real and almost nobody is measuring it.
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JerryRigEverything
JerryRigEverything@ZacksJerryRig·
So this is why elon wanted to rush the IPO so bad... 🤔 China just did it cheaper on their first try. RIP 🔻
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Leo Rebel🇻🇦
Leo Rebel🇻🇦@Ghey724712·
@theAceUrok @newstart_2024 Ask any gay person they will tell you they can’t count how many people they’ve slept with. The only gay person here is you trying to stand up for people who stick their penis in poop
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MOATH | معاذ
هذا الشخص يوتيوبر اسمه "Rusty Cage" قبل ايام حصل خشرة قرادة من نوع Lone Star Tick وبدل التخلص منها قرر يجرب عليها تجارب لمعرفة قدرتها على البقاء حيه، الغريب انه حتى الآن، وثّق عدة محاولات لقتلها منها: - إغراقها في الماء لأكثر من أسبوعين - تجميدها داخل الفريزر لمدة 24 ساعة - تعريضها لموسيقى صاخبة بشكل ساخر - حاول خنقها المصيبه ان كل ذي المحاولات ماقتلتها واظهرت قدره خارقه على البقاء حيه!!!!
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Bryan Johnson
Bryan Johnson@bryan_johnson·
My plan to cure autoimmune gastritis To our knowledge, no one has ever done this to try and cure an autoimmune disease. Context: In May, I got diagnosed with autoimmune gastritis (AIG). We found it by taking a tissue biopsy of my stomach. My immune cells are confused, causing my stomach to eat itself. AIG stops your body from absorbing nutrients like iron and B12, and can eventually lead to cancer. It likely started decades ago when I was diagnosed with hypothyroidism when 21 years old. The thyroid and stomach are closely linked in your immune system. I feel fortunate that I've been taking such good care of my body for the past five years as my condition would otherwise be much more severe. Millions of people are affected by this disease and are undiagnosed. Standard of care tells you that you can’t do anything about it. That’s old fashioned. Here is how we are going to try and cure it: Step 0: find and diagnose the disease ✅ AIG is rarely caught early because symptoms are subtle. Early warnings are low iron and B12, but when hemoglobin and hematocrit look normal, doctors routinely miss it because there are no obvious signs of anemia. A standard colonoscopy won't find it either, because it only checks the lower digestive tract, not the stomach. It was only through a highly targeted stomach biopsy that we found it. Even biopsies can miss it if they don't sample the exact right spots. Most people with AIG go undiagnosed. Step 1: Map my immune system ✅ Last Thursday, I had a blood draw to isolate and decode 1 million of my immune cells. Think of your immune cells as trillions of soldiers. Each carries a unique key designed to unlock and destroy a specific threat, like a virus or bacteria. A standard blood test allows you to see how many soldiers you have, but not their keys. Sequencing one million individual immune cells allows us to read the exact pattern of the teeth on every single key. This is important for my autoimmune gastritis (AIG) because a specific platoon of rogue soldiers has developed keys that unlock an attack on my stomach lining. Right now, we don’t know who they are. This test will inform us of which soldiers have gone rogue and are attacking me from within. Once we know the soldier and key, we know what therapy path to pursue to shut them down. Step 2: Catch the rogue soldiers I will be getting a second biopsy from my stomach because we need to collect live tissue. We are currently planning out the logistics of getting the sample from my stomach to the lab. We need these live cells because the initial blood tests showed the antibodies, which prove that an attack is happening, but doesn’t show us the actual rogue soldier doing the damage which is a T-cell. The live sample will allow us to match the immune system mapping we did to the live T-cells. Step 3: Build an early warning system To keep an eye on the disease as we work towards a therapy, we’re building an early warning system. I'll have my blood drawn every two weeks and we’ll pair that information with wearable data to look for flare ups. This is important because the attack happens without producing symptoms that I can easily feel. Step 4: Create a “Bryan in a dish” testing model, a miniature of my immune system At the same time, we are taking a massive sample of my immune cells and deep freezing them (cryopreservation) for two reasons: a) we’ll create a living lab: using these cells to replicate my immune environment in a lab dish. This allows us to test experimental drugs and therapies on my actual live cells before putting them into my body. b) it creates a back up plan for me by preserving the raw cellular material needed for targeted rejuvenation therapies in the future. Step 5: Build precision guided therapies to end the attack Once we know who the rogue soldiers are, we will engineer a therapy designed uniquely for them. The trick is only turning off the rogue soldiers while leaving all the other healthy ones functioning as they are. For safety checks, we’ll do two test runs: 1) we’ll run the therapy through a computer model that has my biology to evaluate how my molecules interact. 2) We will take my actual cells that we froze in Step 4 and watch them interact for real. If both are successful, we’ll pursue one of four therapies: a) fix the mistake my cells are making, restoring my immune system's natural off switches b) teach the rogue cells to tolerate my stomach instead of attacking it c) design smart molecules that physically plug into the rogue cells and turn them off d) build soldiers who will track down and eliminate the rogue soldiers causing the damage
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Dr. Maalouf ‏
Dr. Maalouf ‏@realMaalouf·
The Egyptian Football Association released a video titled: “The Secret to Victory.” They openly declare that the key to victory is to begin each match by cursing Christians and Jews. Before every game, the team gathers to recite Quranic passages describing Christians and Jews as infidels under Allah’s wrath. Coptic Christians make up 15% of Egypt’s population, yet they are not allowed on the national team. Now, the Islamic team of Egypt has been eliminated by the ‘infidel’ nation of Argentina. Allah was not on their side.
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Thor Torrens
Thor Torrens@ThorTorrens·
Mainstream media misinterprets the temporary upregulation of cellular autophagy from coffee as a true longevity signal, completely ignoring the systemic toll of chronic adenosine receptor antagonism. By artificially blocking adenosine, caffeine forces a state of hyper-vigilance that chronically elevates cortisol and adrenaline, mimicking a perpetual biological emergency that accelerates telomere attrition. This sustained sympathetic dominance forces the mitochondria to run on a high-wear overdrive, generating an unmitigated internal storm of reactive oxygen species that degrades cellular integrity from within. The induced vasoconstriction chokes microvascular blood flow, starving peripheral tissues of vital oxygen and nutrients while systematically disrupting deep, restorative slow-wave sleep—the body's only true window for DNA repair. Coffee does not slow down aging all it does is borrow energy from your biological future, burning out your metabolic engine at a massively accelerated rate.
Rand@rand_longevity

you know coffee slows down your age of aging, right?

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EWTN News
EWTN News@EWTNews·
Pope Leo shook the hands of each of these 20 migrants who just arrived to Europe during his visit to Lampedusa on July 4th, reminding everyone that all human life carries immeasurable worth. A powerful moment of compassion at Europe’s doorstep.
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