Don't Obey

@ze_rusty Come on Jay, ditch the sunglasses….and your UV blocking contacts. I think a lot of people that know about the danger of sunglasses still miss how contacts are acting as a hormone blocker.

"Is anyone else's skin burning faster than normal?" Yes, anyone else who voluntarily blocks their own α-MSH production every time they step outside. UVB at the eye → ciliary ganglia → trigeminal nerve → hypothalamus → pituitary → α-MSH in plasma → systemic skin melanocytes activated Sunglasses block step one. PMID: 12535208

RFK JR - Many don’t realize, the Chickenpox Vaccine Causes shingles Epidemics “When the CDC was thinking about mandating the chickenpox vaccine for your children, they did a study. The person they hired to do that study was a scientist named Gary Goldman, who did a long-term study in California. What he found is that if you give the chickenpox vaccine, mass vaccinate, it stops chickenpox, but causes shingle epidemics later on; which is 20x deadlier. Despite those studies, we mandated for American children in this country, but in Europe they don’t. If you go to the British National Health Service website right now, you can read that it will say, “We do not recommend chickenpox vaccines because it causes shingles epidemics later on… and that’s the problem. (Check the link here: nhs.uk/vaccinations/c…) You can’t say this product is going to prevent this particular disease, but you have to look at the long-term implications.”

FOUR independent datasets from THREE countries have now confirmed that COVID shots induced a CANCER EPIDEMIC 1. U.S. government SEER cancer data (+6.4% surge in early-onset cancers since 2021) 2. CDC WONDER mortality data (138,000 excess cancer deaths since 2021) 3. South Korean study of 8.4 MILLION (increased risk of SIX major cancers) 4. Italian study of 300,000 (increased risk of THREE major cancers) WHY ISN’T THIS FRONT PAGE NEWS?

THE SUNRISE IS THE MOST POTENT CIRCADIAN STIMULUS. A 2020 paper published in Current Biology identified a previously unknown retinal circuit explaining precisely why the spectral contrast of sunrise so powerfully entrains the circadian system. The key neuron is the M1 intrinsically photosensitive retinal ganglion cell (ipRGC), which projects directly to the suprachiasmatic nucleus (SCN), the brain’s master circadian pacemaker. In primates, M1 ipRGCs are wired to perform a spectral comparison between yellow/red and blue light via two simultaneous pathways. ***This cone-based circuit is just one of several mechanisms by which morning light entrains the circadian system. Going outside after sunrise still delivers meaningful melanopsin stimulation as overall irradiance builds, and that sustained signal remains highly beneficial. The spectral contrast mechanism described here is simply the most precisely tuned and potent stimulus the system has, one that outdoor morning light delivers far more effectively than any indoor environment. As yellow and red wavelengths increase at sunrise, L and M cones drive LM-ON bipolar cells, which directly excite the M1 ipRGC. Simultaneously, the relative decrease in short-wavelength light reduces S-cone activation, quieting S-ON bipolar cells, which reduces drive to a newly identified S-cone amacrine cell, releasing its inhibitory input onto the ipRGC. Disinhibition and excitation converge on the same cell simultaneously. Melanopsin, the ipRGC’s intrinsic photopigment peaking at ~480nm, is slower and requires sustained high irradiance, taking over as morning light intensity builds. The result is a temporal relay: the cone circuit delivers a rapid spectral signal at the horizon transition, then melanopsin sustains entrainment through the morning. No indoor lighting replicates this. The sunrise delivers the exact stimulus this circuit evolved over hundreds of millions of years to detect. #science #circadian #sunrise #neuroscience #biology

The problem with most supplements is the deuterium they deliver. Stephanie Seneff, MIT researcher: "People are loading up on supplements that are actually hurting them — they're not supplying the low deuterium resource that would have happened if it had been biological." Most supplements are made in chemistry labs. The molecules are chemically identical to their natural counterparts. But they lack one critical property: deuterium depletion. Deuterium is a heavy form of hydrogen that damages ATPase pumps in the mitochondria. Melatonin is the clearest example. Your gut produces 400x more melatonin than your pineal gland — most of it inside mitochondria. Seneff: Melatonin is not primarily a sleep hormone. It is a deuterium depletion system. Here's the mechanism: Gut microbes produce hydrogen gas that is 80% deuterium depleted. That gas feeds a chain of conversions — producing methyl and acetyl groups that are severely low in deuterium. Those methyl and acetyl groups get attached to serotonin, converting it into melatonin. Each melatonin molecule now carries depleted hydrogen — ready to be delivered to the mitochondria. Inside gut cells (enterocytes), an enzyme called CYP2C19 strips the methyl group off melatonin. Each time it does, it releases four molecules of deuterium-depleted water directly into the mitochondria — protecting the ATPase pumps that generate your cellular energy. Four depleted water molecules. Per cycle. To the ATPase pumps that need them most. When melatonin is made synthetically — which is virtually all commercial melatonin — the methyl and acetyl groups come from bulk chemicals made in a lab. Random high deuterium content. The biological depletion step never happened. Your body cannot tell the difference. Sleep improves. Antioxidant effects occur. But the deuterium depletion cycle doesn't run. The mitochondria don't get what they actually need. The short-term benefit masks the long-term harm. The TMAO (Trimethylamine N-oxide) evidence: TMAO is a marker for deuterium toxicity — deuterium-loaded methyl groups accumulating systemically. People who ate eggs — no TMAO increase. People who took synthetic choline supplements — elevated TMAO. The mechanism: enzymes that metabolize methyl groups can detect deuterium — and refuse to process it. The trimethylamine survives in the gut. Gets oxidized in the liver. Becomes TMAO in the blood. The same problem applies to: N-acetylcysteine (NAC) — the acetyl group is low deuterium from gut microbes, unpredictable when synthetic. Choline bitartrate — Seneff: "If you're taking choline bitartrate, you need to stop." Methionine — methionine-deficient rats lived longer in one study. Seneff's interpretation: methionine restriction extended lifespan not because methionine itself is harmful — but because the rats stopped receiving deuterium-loaded synthetic methionine. Their gut microbes produced it naturally — low deuterium. The rats getting synthetic methionine wrecked their mitochondria with deuterium-enriched methyl groups. The deficient rats didn't. Methylated B vitamins — likely synthetic, likely the same problem. The studies testing these supplements never account for the fact that they're synthetic. They have no idea that's even a variable worth measuring. What to do instead: - Get methionine from meat, fish and eggs — not synthetic amino acid supplements. - Get choline from eggs and animal foods — not choline bitartrate. - Get tryptophan from food — chicken, turkey, beef, pork, fish, eggs, hard cheeses (parmesan, cheddar). Your gut microbes convert it through the biological pathway naturally, producing depleted melatonin the way biology intended. One study: tryptophan loading increases serum melatonin 4-fold — even in rats without a pineal gland, confirming the melatonin was gut-sourced not pineal-sourced. - Animal fats — butter, tallow — are among the lowest deuterium foods available. Derived from acetate produced by gut microbes from deuterium-depleted hydrogen gas. The same pathway that makes biological methyl groups low in deuterium. - Eat certified organic. Glyphosate disrupts the gut microbiome — which disrupts the entire deuterium management system upstream. - Fermented foods support acetate production and the whole chain. Whenever the food is fermented, the microbes are making nutrients that are low in deuterium. - Keep your gut microbiome healthy. It is your primary deuterium management system. Seneff is 78 years old. Still writing papers. Mentally sharp. Doesn't take any supplements. "I don't take any supplements. None of these organic molecules. None." The supplement industry sells you the molecule. They don't sell you the mechanism biology built into the production process.

The single LARGEST vaccine–dementia study ever conducted (n=13.3 MILLION) found that adult vaccines (flu, pneumococcal, shingles, tetanus, diphtheria, pertussis) increase risk of DEMENTIA (+38%) and ALZHEIMER’S (+50%) for a DECADE. The more doses, the higher the dementia risk.

@JamieAA_Again If anyone is interested, the source videos is worth a watch. rumble.com/v1yj8a0-the-em…

Dr David Baltimore the fraudulent Nobel Prize winner. Here he is floundering at being asked a basic question relating to isolation and purification. This man was supposedly a NPW for finding "Reverse Transciptase" some enzyme related to "HIV".

@prospertarian @DrJackKruse I try to unravel it every day...it's good to stretch the brain first thing in the morning. Even if you don't understand it all (nobody does), picking up what you can will change your paradigm.

As a podcaster with hundreds of interviews under my belt, I instantly know when someone is full of shit. And it's mind-blowing the people that say they understand @DrJackKruse work or be is a mentor… few have any grasp. Like at all. And I certainly don't. But I know damn well when the pseudo Mito experts speak.

@the_no_mind One of my favorite quotes is that "life is nothing but an electron looking for a place to rest". Györgyi

Life runs on electrons, not calories. Albert Szent-Györgyi, Nobel Prize winner, 1937: "What drives life is a little electric current, kept up by the sunshine. All the complexities of intermediary metabolism are but lacework around this basic fact." "Life is driven by electrons, by the energy given off by these electrons while cascading down from the high level to which they have been boosted up by photons." "Strictly speaking, an electron has no energy in itself, as water has no energy. Water can give off energy when it drops from a higher to a lower level — say from the top to the bottom of Niagara Falls. Similarly, the electron can give off energy and drive the living machine by dropping from a higher to a lower energy level." "The foodstuff is essentially an H donor while O₂ is an H acceptor. H is the fuel of life." Underneath all metabolism is one transaction: hydrogen donates an electron. Oxygen accepts it. Life runs on single electrons moving through a regulated physical system. Not on calories.

@LxngevityLab Sinclair is a fraud, do a little digging on his resveritol scam … and he is not the first to reverse aging. He isn’t even close to what BKWRD.com has done. They have already demonstrated multi-system age reversal in humans.

The first scientist to ever reverse human aging just dropped the craziest interview on the internet. Here are 8 facts David Sinclair revealed about aging that will leave you speechless (THREAD): 1. Cancer & Alzheimer's are symptoms of the same disease.

Post-Pandemic Week 49 2025 Update The Bad News: Excess Cancer Mortality has accelerated beyond even its old elevated trend. Elevated at 10.1% over baseline. PFE here is only 1.1-pts of this excess (11%). Perhaps this is why we have observed elevated cancer treatment expenditures, diagnoses, drug allocations, and new patient social chatter — all inflecting in relation to the very same strike point (Week 14 of 2021). This is not good news, and overshadows all the other good or encouraging news about US Mortality trends. The signal is clear. TES was right to have raised the alarm over this signal 5 years ago. 😑

Today years old 🧐🧐🧐

The Hidden Circuit: How Melanin and Fascia Turn Your Body into a Living Semiconductor Beneath the skin and around every muscle, a shimmering, collagen-rich tissue called fascia wraps the body in a continuous tensional network. For centuries, anatomists dismissed it as mere packing material. Meanwhile, melanin—the pigment that colors skin, hair, and eyes—was studied mostly for its role in sun protection and camouflage. Now biophysicists are discovering that these two systems, long considered biological footnotes, are in fact partners in one of the strangest electrical circuits in nature. “Fascia is not a passive scaffold,” says Marco Bordoni, a physicist-turned-fascia researcher at the University of Padua. “It’s a liquid-crystalline semiconductor that spans from your fingertips to your spine. And melanin appears to be its co-conductor.” The Collagen Antenna Collagen, the main protein in fascia, arranges itself into triple-helical cables that behave like optical fibers and piezoelectric crystals at the same time. When you stretch or compress fascial tissue—every time you run, jump, or simply stand up—the collagen lattice generates tiny electric fields. These fields are not random noise. They are coherent enough to drive proton currents along nanoscopic layers of highly ordered water that coat every collagen fiber. This “fourth phase” water, first described by Gerald Pollack at the University of Washington, absorbs ultraviolet light at 270 nanometers and re-emits it as infrared photons—a built-in energy transduction system running quietly under your skin. Enter Melanin, the Black Semiconductor Melanin has baffled physicists for decades. Unlike typical organic molecules, it absorbs light across almost the entire spectrum, from ultraviolet to near-infrared, then dissipates the energy with almost no fluorescence. Where does the energy go? In a series of papers beginning in 2012, a team led by A. Bernard Mostert at Swansea University showed that hydrated melanin conducts both electrons and protons, switching from insulator to near-metal depending on water content. In 2021, Carlos Solís and colleagues at the National Autonomous University of Mexico demonstrated that melanin can photocatalytically split water into protons, electrons, and oxygen—the same reaction that powers photosynthesis—using nothing more than ultraviolet light. “Melanin is basically an amorphous, biodegradable solar cell,” says Paul Meredith, a physicist at the University of Queensland and co-author of many of the seminal melanin-conduction studies. A Body-Wide Optoelectronic Network The surprise came when researchers started looking deeper than the epidermis. In 2020, Carla Fede and her group in Padua published micrographs showing melanosomes—tiny melanin granules—inside myofibroblasts of the deep fascia, especially in individuals with darker skin. In some mammals (whales, certain bats, and horses), entire sheets of deep fascia are visibly black with melanin. When these melanized fascial cells are mechanically deformed, their electrical conductivity changes far more dramatically than in non-melanized tissue. The reason, Bordoni’s lab found, is that mechanical strain alters the hydration shell around melanin particles, flipping their conductivity like a transistor. The result is a distributed circuit: sunlight hits skin melanin → energy is converted to heat, protons, and electrons → some of that charge migrates along structured water highways in the fascia → mechanical movement of the fascia generates additional piezoelectric currents → melanin modulates the signal. “It’s as if evolution wired us with a photovoltaic-piezoelectric skin that extends all the way to the tendons,” Bordoni says.

@Alec_Zeck That's great!🤣

😂😂😂😂😂😂

Dear conspiracy theorists.. sadly, you were right again… 🚨 Dr. Robert Malone: Declassified Docs Expose U.S. Military Releasing 282,800 Radioactive Ticks, Sparking Lyme Disease Epidemic and 40-Year Cover-Up - The U.S. military released 282,800 radioactive lone star ticks (labeled with Carbon-14) across Virginia sites along bird migration routes from 1966–1969; before the experiments, these ticks were not found north of the Mason-Dixon Line, but they soon established populations on Long Island for the first time. - CIA operatives under Operation Mongoose (1962) dropped infected ticks on Cuban sugarcane workers via nighttime C-123 flights; one operative’s infant son suffered a life-threatening 105°F fever requiring emergency tracheotomy after family contamination. - Plum Island Animal Disease Center (under Army Chemical Corps) conducted open-air tick experiments with containment failures: test animals mingled with wild deer and birds, and deer from nearby Lyme, Connecticut, swam to the island while birds fed on insects—Lyme, CT, is only 13 miles away and became the namesake epicenter in 1975. - Willy Burgdorfer (who identified the Lyme bacterium in 1982) discovered a second pathogen called the “Swiss Agent” (Rickettsia helvetica) in patient samples but deliberately omitted it from his published research; materials found in his garage after his 2014 death proved 40+ years of suppression of co-infection data that could explain chronic Lyme treatment failures. - Under Project 112 (1962–1974), the Pentagon ran 134 bioweapons tests (plus hundreds more classified), investing $3–4 billion and building capacity to produce 100 million infected mosquitoes and 50 million fleas per month; the program was “categorically denied” by the military for nearly 50 years until 2000. - Operation Big Itch (1954) successfully dropped 670,000 tropical rat fleas from cluster bombs to prove the weapons could incapacitate an entire battalion-sized target area for up to a full day. - Multiple tick-borne diseases (Lyme arthritis, babesiosis, Rocky Mountain spotted fever) erupted simultaneously around Long Island Sound right after the tick releases (1968–1972), clustering statistically around Plum Island—an anomaly the article attributes to possible lab enhancement or accidental release (45% probability per the analysis). - Burgdorfer, recruited in 1951 for tick weaponization and linked to Nazi scientists brought via Operation Paperclip, left a cryptic note before dying: “I wondered why somebody didn’t do something,” and in 2013 video testimony insinuated an accidental release while admitting he “didn’t tell you everything.” These claims are based on a review of 41 primary declassified sources, testimony, and suppressed research presented in the article. malone.news/p/declassified…

@stringerbell99 @TrueLibertyX @ScottAppliedSci

These are studies that don’t fully account for reverse causation. Many chronic conditions cause low cholesterol, not the other way around. If low cholesterol caused an increase in mortality, people with genetically very low cholesterol would live the shortest. Instead, they live longer than average.

Normal human LDL is in the 40-70 mg/dL range. There’s no mistake in the guidelines.

@TrueLibertyX @ScottAppliedSci Not junk science. Pretty simple...178k patients, measured cholesterol over 20 yrs and watched who died, all-cause mortality. The hazard ratios speak for them selves.

@PharmerProper @ScottAppliedSci Cite the source, there are a few papers like this that are junk science.

@KenDBerryMD @ScottAppliedSci If you follow recommendations of 40-70 LDL, you have a 50% increased chance of death vs someone in the 100-189 range. That's all you need to know. 178,000 patients in this study.

@KenDBerryMD @ScottAppliedSci This says it all: Conclusions Among primary prevention-­ type patients aged 50–89 years without diabetes and not on statin therapy, the lowest risk for long-­ term mortality appears to exist in the wide LDL-­ C range of 100–189 mg/dL, is much higher than current recommendations.

@TrueLibertyX @ScottAppliedSci Conclusions Among primary prevention-­ type patients aged 50–89 years without diabetes and not on statin therapy, the lowest risk for long-­ term mortality appears to exist in the wide LDL-­ C range of 100–189 mg/dL, which is much higher than current recommendations.

@TrueLibertyX @ScottAppliedSci Only if you want a 50% chance of increased death. Hazard ratios of 178,000 patients don't lie.