Farving🙆⭐️ (@FarvingCo) - Twitter Profili

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The FDA banned it. WADA banned it. The NFL, UFC, NBA, MLB, and NCAA banned it. Not a steroid. Not HGH. Fifteen amino acids from human stomach acid. Scientists severed a rat’s Achilles tendon. Gave it this compound. The tendon grew back stronger than it was before the cut. It grew new blood vessels into dead tissue and sealed a broken gut lining. Then it shut down the inflammatory cascade that drives insulin resistance. It rebalanced serotonin and dopamine in the brain. Not up. Not down. Back to center. 544 studies since 1993. No lethal dose ever found in any species at any dosage. All preclinical. Animal models. Zero completed human clinical trials. You can buy it for less than a single ibuprofen. The DOJ forced a pharmacy to surrender $1.79 million for distributing it. It’s called BPC-157. And it’s still available. 🧵

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Farving🙆⭐️@FarvingCo·3h

Every claim has a receipt: Achilles tendon recovery → PMID: 14554208 Blood vessel growth + gut barrier repair → PMID: 27847966, reviewed in PMID: 32445447 Inflammatory suppression → reviewed in PMID: 32445447 Serotonin/dopamine normalization → PMID: 27138887 2025 systematic review (544 screened, 36 included, no toxicity) → PMID: 40756949

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Farving🙆⭐️@FarvingCo·3h

This is the one I take → Oral tablet that dissolves across the full GI tract. Not just the stomach. No needle. Code GUNNAR saves you 15% barrier.co/?ref=GUNNAR

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Farving🙆⭐️@FarvingCo·3h

The FDA banned it. WADA banned it. The NFL, UFC, NBA, MLB, and NCAA banned it. Not a steroid. Not HGH. Fifteen amino acids from human stomach acid. Scientists severed a rat’s Achilles tendon. Gave it this compound. The tendon grew back stronger than it was before the cut. It grew new blood vessels into dead tissue and sealed a broken gut lining. Then it shut down the inflammatory cascade that drives insulin resistance. It rebalanced serotonin and dopamine in the brain. Not up. Not down. Back to center. 544 studies since 1993. No lethal dose ever found in any species at any dosage. All preclinical. Animal models. Zero completed human clinical trials. You can buy it for less than a single ibuprofen. The DOJ forced a pharmacy to surrender $1.79 million for distributing it. It’s called BPC-157. And it’s still available. 🧵

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Farving🙆⭐️@FarvingCo·14h

The study cited: Cani et al. 2007, published in Diabetes (PMID: 17456850). Chronic LPS infusion alone — no dietary change — triggered weight gain, visceral fat accumulation, and insulin resistance in mice. The gut barrier is the bottleneck. BPC-157’s role in sealing that barrier: PMID: 32445447, PMID: 27847966.

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Farving🙆⭐️@FarvingCo·14h

This is the BPC-157 I use daily → barrier.co/?ref=GUNNAR Barrier — oral tablet that dissolves across the full GI tract. Not just the stomach. No needle. Code GUNNAR saves 15%.

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Farving🙆⭐️@FarvingCo·16h

Why does no one talk about the bacterial toxin that triggers your body to STORE BELLY FAT? Your doctor rarely tests for it. Your diet alone can’t fix it. When the wrong bacteria overgrow, they release a toxin called LPS into your bloodstream. It targets visceral fat cells directly: → Stubborn belly fat that won’t respond to calorie cuts → Brain fog and afternoon crashes you’ve blamed on sleep → Insulin resistance your doctor can’t explain → Bloating that makes you look 6 months pregnant by dinner I lived all four. Clean eating, consistent training, perfect sleep — my gut didn’t care. Same bloat every night. Same soft midsection. Same belt notch for twelve months. Then I found the toxin actually doing it. Chronic LPS infusion alone — no change in diet or calories — increased visceral fat to levels matching high-fat diet groups. Body composition shifted without a single extra calorie (PMID: 17456850). This wasn’t a discipline problem. It was a barrier problem. BPC-157 — a peptide from human gastric juice — seals the leaks in your gut lining. No large human trials yet, but preclinical consistency across dozens of studies is unusually strong. I started BPC-157 in June. By week two the bloating was noticeably flatter. By week five my belt moved one notch tighter — after twelve months of discipline changing nothing. If your belly fat won’t budge despite eating clean and training hard — you don’t have a discipline problem. You have a barrier problem. The exact BPC-157 I use is linked in the comments.

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Farving🙆⭐️@FarvingCo·20h

Reduced S. mutans in 15 minutes. Dropped levels further in three weeks. This is the one I chew daily — Chios mastic from @GrecoGum. Code GUNNAR saves you 10%. grecogum.com/GUNNAR

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Farving🙆⭐️@FarvingCo·21h

The bacterium destroying your teeth is also inflaming your heart. S. mutans is the #1 cause of cavities. But that’s the least of your problems. Every time you chew, brush, or get dental work — it enters your bloodstream. In under 60 seconds it can reach your heart. Once there, it embeds in atherosclerotic plaques and heart valve tissue — driving the same inflammation linked to heart attacks and strokes. S. mutans was detected in 69% of heart valves and 74% of atheromatous plaques — more frequently than any other oral bacterium tested. (PMID: 16954266) Your mouth bacteria don’t stay in your mouth. And no one is connecting your dental health to your cardiovascular risk. One compound shown to reduce S. mutans in the lab and in humans: Mastic gum. 15 minutes of chewing significantly reduced salivary S. mutans counts vs placebo. (PMID: 16343417) Three weeks of daily use dropped mutans streptococci levels even further. (PMID: 25628697) Your toothpaste kills surface bacteria. It doesn’t touch what’s already in your bloodstream. I linked the mastic gum I use in the comments.

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Farving🙆⭐️@FarvingCo·20h

The mastic gum I use daily — high-dose Chios mastic, the same variety used in the studies cited above. Killed P. gingivalis at 2.4 μg/mL. Published research. Not a wellness trend. Code GUNNAR saves you 10%. grecogum.com/GUNNAR

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Farving🙆⭐️@FarvingCo·23h

There’s a bacterium in your mouth that’s been found in the brains of Alzheimer’s patients. It’s called P. gingivalis. It produces LPS that enters your bloodstream through inflamed gums. Once systemic, it triggers a cascade that drives chronic inflammation and insulin resistance. Mice given P. gingivalis orally developed endotoxemia, increased visceral fat, and impaired glucose tolerance. (PMID: 28067105) Your mouth is the first firewall. If it’s breached, your gut, brain, and metabolism pay for it. Its proteases (gingipains) have been found in Alzheimer’s brains — correlating directly with tau pathology. (PMID: 30746447) No one connects oral health to belly fat or neurodegeneration. But the mechanism is sitting right there in the literature. One of the few compounds shown to kill P. gingivalis without destroying healthy tissue: mastic gum. Mastic extract killed P. gingivalis at just 2.4 μg/mL. The strongest active compound identified: isomasticadienolic acid. (PMID: 16822220) Your mouthwash isn’t enough. The bacteria driving your inflammation might not be in your gut. It might be in your gums. I use @GrecoGum mastic gum. Code GUNNAR saves you 10%. Link in the comments.

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Farving🙆⭐️@FarvingCo·20h

First natural compound to kill H. pylori. Published in the New England Journal of Medicine. 1998. This is the one I use — high-dose Chios mastic from @GrecoGum. Code GUNNAR saves you 10%. grecogum.com/GUNNAR

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Farving🙆⭐️@FarvingCo·21h

Unexplained bloating. Acid reflux. Belly fat that won’t budge. The upstream cause no one tested for: H. pylori. It infects ~50% of the global population. Most people never know they have it. It burrows into your stomach lining and triggers chronic low-grade inflammation throughout your body. It also breaks down your stomach’s barrier — the wall keeping everything you swallow out of your bloodstream. In adults under 50, H. pylori infection increased the risk of metabolic syndrome by 3.7x. Eradication improved insulin resistance, lipid profiles, and inflammatory markers. (PMID: 25984214) No one connects their acid reflux to their belly fat. But the mechanism is the same bacterium. Mastic gum was the first natural compound shown to kill H. pylori. Published in the New England Journal of Medicine in 1998. (PMID: 9874617) It killed all strains tested — including metronidazole-resistant ones — at just 0.06 mg/mL. A later RCT confirmed bactericidal activity in vivo. Mastic gum alone eradicated H. pylori in 30-38% of patients. (PMID: 19879118) A tree resin. Published in the NEJM. Killing antibiotic-resistant bacteria. 50% of the world is infected. The solution was published in the NEJM 27 years ago. And your doctor still hasn’t mentioned it. I linked the mastic gum I use in the comments.

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Farving🙆⭐️@FarvingCo·20h

Severed ligament. Drinking water delivery. Full recovery. The preclinical data on BPC-157 is hard to ignore. This is the one I use — BPC-157 from @barrierhealth. Code GUNNAR saves 15%. Link below. barrier.co/?ref=GUNNAR

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Farving🙆⭐️@FarvingCo·20h

A rat had its knee ligament SEVERED COMPLETELY. They gave it BPC-157 in drinking water. Full recovery. The mechanism: BPC-157 upregulates VEGF receptor expression. New blood vessels form in avascular tissue. Fibroblasts finally get the oxygen and nutrients to lay down organized collagen. Ligaments don’t heal because they don’t get blood flow. BPC-157 fixes the supply chain.

Alfred 🏄🏻‍♀️@HealthyAlfred

They cut a rat’s knee ligament CLEAN THROUGH. Gave it oral BPC-157 in drinking water. 100% recovery. Biomechanically. Functionally. Structurally. From DRINKING WATER… (PMID: 20225319) Your knee hasn’t been the SAME since that twist. Your shoulder BUCKLES when you press. Your ankle still GIVES OUT on stairs. You were the one who never sat out. Never skipped a session. Never made excuses. Now you modify EVERYTHING. And at some point you stopped believing it would heal. You just protect it now. Ligaments barely get blood flow. That’s why yours has been “almost healed” for 2 YEARS. Almost. Never fully. Never COMPLETELY. BPC-157. 15 amino acids. Already in your stomach juice. Not invented — DISCOVERED. → Severed ligament: COMPLETE recovery → Oral: IDENTICAL results to injection → Adverse effects: NONE found (PMID: 20225319) → NSAID damage reversed: ORALLY (PMID: 21295044) → Intestinal fistulas closed: via DRINKING WATER (PMID: 34267654) Ibuprofen? Numbs the signal your body needs to START healing. BPC-157 → fibroblasts activate → collagen organizes → ligament REBUILDS Week 2-3: Stiffness LOOSENING Week 4-6: Stability RETURNING Week 6-8: Loading without FEAR My knee was unstable for over a year. I could walk fine. But every squat, every cut, every unexpected step — I BRACED. Started oral BPC-157. Week 3 the joint felt noticeably tighter. Week 8 I squatted without the brace. The knee held. Not perfect — but the first time in a year it was getting STRONGER instead of just surviving. Your ligament isn’t “just like that now.” It never got the signal to FINISH. CHECK COMMENTS FOR BPC-157! Rest HOPES for healing that never comes. BPC-157 SENDS the signal to complete it. BPC-157 is not FDA-approved. Preclinical evidence. Not medical advice.

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Farving🙆⭐️@FarvingCo·20h

@AdmetosL Added it

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Spirit of Admetos@AdmetosL·20h

@FarvingCo i see no other comments under this post

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Farving🙆⭐️@FarvingCo·20h

@AdmetosL One sec let me add the mastic gum I use

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Farving🙆⭐️ retweetledi

Alfred 🏄🏻‍♀️@HealthyAlfred·21h

69% of heart valves. 74% of atherosclerotic plaques. All from a bacterium most people think only causes cavities. @farvingco connected S. mutans to cardiovascular inflammation with the actual research. Then showed what kills it. This is why I’ve been chewing mastic gum every day.

Farving🙆⭐️@FarvingCo

The bacterium destroying your teeth is also inflaming your heart. S. mutans is the #1 cause of cavities. But that’s the least of your problems. Every time you chew, brush, or get dental work — it enters your bloodstream. In under 60 seconds it can reach your heart. Once there, it embeds in atherosclerotic plaques and heart valve tissue — driving the same inflammation linked to heart attacks and strokes. S. mutans was detected in 69% of heart valves and 74% of atheromatous plaques — more frequently than any other oral bacterium tested. (PMID: 16954266) Your mouth bacteria don’t stay in your mouth. And no one is connecting your dental health to your cardiovascular risk. One compound shown to reduce S. mutans in the lab and in humans: Mastic gum. 15 minutes of chewing significantly reduced salivary S. mutans counts vs placebo. (PMID: 16343417) Three weeks of daily use dropped mutans streptococci levels even further. (PMID: 25628697) Your toothpaste kills surface bacteria. It doesn’t touch what’s already in your bloodstream. I linked the mastic gum I use in the comments.

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Farving🙆⭐️@FarvingCo·1d

@Tuppytubberman That’s awesome let’s go

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TS@Tuppytubberman·1d

@FarvingCo This shit works. My waist has drastically shrunk and I have only dropped a few lbs. Not enough to explain

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Farving🙆⭐️@FarvingCo·2d

You can’t lose that belly fat because a toxin is leaking from your gut into your bloodstream. It’s called LPS. It drives insulin resistance and forces your body to store visceral fat. In a double-blind trial, 300mg of lactoferrin daily reduced visceral fat by 14.6 cm² in 8 weeks. Placebo group: 1.8 cm². No diet change. No exercise change. Lactoferrin binds LPS directly and prevents it from crossing your gut lining into circulation. Stomach acid degrades most of it before it reaches your lower gut. Enteric coating lets it arrive intact. I pinned the one I use in the comments. That belly fat isn’t a willpower problem. It’s a toxin problem. PMID: 20691130, 22101278

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Farving🙆⭐️@FarvingCo·1d

@goforthdancing I lost 2 inches off my waist in 2 months

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DanceWithMe@goforthdancing·2d

@FarvingCo It works.

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Farving🙆⭐️@FarvingCo·1d

@TheFalcoEffect 99% of people don’t know this

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Falco@TheFalcoEffect·2d

@FarvingCo LPS-driven fat storage is genuinely underrated. Most people are out here blaming carbs while their gut barrier is quietly leaking poison into circulation.

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Farving🙆⭐️

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