A. A mitochondria does this every day, but food gurus never speak of this. They take an electron off light hydrogen (H+) and put it inside a massive electric field derived from the inner mitochondrial membrane adjacent to the spinning Fo head. This creates magnetic containment, and Voila: Nature turns your food stuff into a new form of matter.

H+ becomes a liquid metal. This is why it is life's chameleon and why our matrix is filled with ionized H+. Your food guru just keeps shitting the bed, which is why their Rx never reverses much.Image
B. You think this is common knowledge? It is not.

It is decentralized wisdom that centralized minds just found. sciencealert.com/hydrogen-has-b…
C. The Setup: Mitochondria’s Electric Forge

Mitochondria’s IMM is a beast—cristae folded tight, hosting the electron transport chain (ETC).

Complexes I-IV pump protons (H⁺) out, building a proton-motive force (PMF): 150-200 mV, pH drop of 1 unit, electric field screaming at 30 million V/m (Mitchell, 1961).

That’s no typo—30 MV/m, dwarfing lab toys.

ATPase’s F₀ head spins in this, driven by H⁺ rushing back, churning ATP.

Nature's twist: strip an electron off “light hydrogen” (H, not deuterium), slam it into this field, and—bam—liquid-metal H⁺ emerges, a chameleon in the matrix.Image
D. Hydrogen to Liquid Metal: The Science

That Science Alert piece above flags Harvard’s 2017 feat—Isaac Silvera and Ranga Dias squeezed hydrogen gas between diamond anvils to 495 GPa (4.95 million atm), stripping electrons, & hitting metallic hydrogen.

It’s shiny, conductive, & a liquid under insane pressure and cold (-270°C).

Critics (e.g., Loubeyre, 2017) doubted it held—diamonds cracked, data wobbled—but the concept’s legit: break H₂ bonds, free electrons, and atomic hydrogen densifies into a metal-like state. Imagine that.Image
E. Mitochondria don’t hit 495 GPa, but Nature's play is clever. The IMM’s electric field—30 MV/m—approaches dielectric breakdown strength (think lightning in a cell).

How much do you know about the Casimir effect?
Food gurus are drooling on themselves now. They have no idea where the story is headed.

H⁺ isn’t H₂ gas; it’s ionized, electron-stripped by ETC (NADH → NAD⁺ + H⁺ + e⁻). The F₀ head, spinning at 9,000 RPM, generates a local magnetic field—Faraday’s law in nano-scale (H⁺ flow = current).

Did you know that the electromagnetic force gets stronger as the scale shrinks? The food gurus have no idea about this or why it is important.

Not fusion-level containment, but enough to torque H⁺ into a dense, ordered state near the membrane. Liquid metal? Not bulk, but a fleeting, metallic-esque phase—high proton density, charge coherence, fluidity.Image
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F. Why It Works: Life’s Chameleon

Matrix H⁺ isn’t gas or tame water—it’s ionized, buzzing, a plasma Lite. The IMM’s field and F₀’s magnetism herd it, per spintronics we mused—chiral currents align it.

This “liquid-metal” H⁺ drives ATPase, shuttles electrons, buffers pH.

It’s a shape-shifter—adapting to light’s flux (sun’s EMF), food’s chaos, & latitude's whims. No optimal diet? Here’s why—H⁺ morphs to the beat, not the meal. Anubians thrived on this; pharaohs, light-starved, lost it.Image
G. Biochemist Shock, Mitochondriac Nod

Biochemists gawk—textbooks call H⁺ a proton, not a metal. They’re stuck on equilibrium, not Prigogine’s dissipative flux.

Mitochondriacs? It is their daily bread—mitochondria bend physics, not just burn sugar.

The matrix teems with ionized H⁺ because this trick sustains life’s dance—energy, water, spin—all in one. That 2017 lab stunt?

Mitochondria do it sans diamonds, with every breath we take.Image
H. I'm done dealing with idiots and I hope my science has convinced some of you to stop dealing with them too.

The Natural Flow is the way to go.

Mitochondria strip H, juice it in a 30 MV/m field, spin it with F₀’s magnetic grip—liquid-metal H⁺ powers the show.

It’s why diets don’t lock; it’s why light rules.
Game, Set, match bitches. The centralized biology of food is too tame for this decentralized wizardry.

Next spark—how do we catch this H⁺ mid-act? Flow harder with me in that decentralized river to find out.Image
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More from @DrJackKruse

Oct 11
What do you know about the Stiles-Crawford effect in a healthy eye? What if I told you this effect is how we sharpen central vision and narrow the periphery of the retina from too much blue light. Would you believe it? Did you know melanopsin has a specific topographic map on a healthy retina? A lesson no has taught you is incoming.Image
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2. All opsins are topologic insulators. You might want to read that threadroll above now to understand topology well.

Topology changes in a cell = geometry change of cristae = UPE change from mitochondria = the optical signal changes in the same tissue altering physiology.

So what happens if you sustain mitochondrial damage in your retina's colony of mitochondria to the Stiles Crawford effect?

What are the implications?Image
3. The Stiles–Crawford effect (SCE) is the human eye's phenomenon of reduced light sensitivity when light enters the pupil from its periphery compared to the pupil's center. This effect is due to the optical properties of photoreceptors, which act as waveguides and are aligned to channel light towards the fovea, the central point of vision. The SCE makes vision less sensitive to light entering the periphery, thus reducing glare and improving visual clarity. It also keeps a lid on the amount of blue light the periphery the retina gets.

This sharpens vision, makes myopia, glaucoma, cataracts, hyperopia, and AMD almost impossible to get. Makes one resistant to mental illness too. Makes one impervious to diabetic transformations. Makes neurodegeneration rare.

You feeling me yet?Image
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Read 13 tweets
Oct 10
Another new podcast from me with Smuggling Hope. It is good one on mental health because it explains how biomolecules absorption and emission spectra's determine reality or determine which mental illness one gets.

This is the information why Jordan Peterson is sick and why he and his daughter have stumbled multiple times in getting him well.
ivoox.com/.../exposing-t…...
Biophotons are ultra-weak light emissions produced by living organisms, thought to arise from metabolic processes like oxidative reactions in mitochondria. Centralized scientists and AI bots hypothesized them to play a role in cellular communication, potentially influencing gene expression or signaling pathways. FIAF, also known as angiopoietin-like protein 4 (ANGPTL4), is a protein produced by tissues like fat and the gut, and it’s a key player in lipid metabolism and microbiome construction. Neither understand how UPEs control FIAF. If the UPE is coherent then FIAF inhibits lipoprotein lipase, affecting how fats are stored or broken down, and its expression ramps up during fasting. The microbiome, meanwhile, is the community of gut microbes that can shift in response to diet, fasting, or host metabolism, influencing energy balance and health. If the UPEs in mitochondria is not coherent, the UPE changes and mental illness becomes more probable. You cannot burn fat so it changes neural signaling.

Centralized scientists and technocrats who build AI systems will say no direct study says “biophotons control FIAF to affect the microbiome,” but we can hypothesize based on related mechanisms. This is patently false. Why?

FIAF has known absorption and emission spectra to light frequencies. Because of that, a study is superfluous because each chemical in the world has an optical fingerprint. Just because a scientist has not published the work is immaterial to this BASIC biophysical fact in spectroscopy. This was what I brought Ray Peat over ten years ago, and he was impotent enough to answer my critiques of his work. This podcast covers these details.Image
2. Is nerve pain caused by a Lyrica deficiency?
Is Lyme disease linked to a lack of doxycycline?
Is depression due to Prozac deficiency.
Are heart attacks are due to Lipitor deficiency.
Is obesity due to Ozempic deficiency.
Are Headaches due to Tylenol deficiency?
Is Bipolar disorder due to lithium deficiency?
Any questions?
You've been conditioned by centralized medicine to ask the wrong question.
You have a solar deficiency combined with a nnEMF toxicity problem.

This alters the UPEs your mitochondria make and it is this light that changes the neural tracks that make you mentally ill. This is why your Bipolar Disorder exists. The defect is not in you; it is in your environment.Image
3. Light exposure,say, sunlight or specific wavelengths impacts circadian rhythms via the suprachiasmatic nucleus in the brain, which regulates hormones like dopamine, GABA,melatonin and cortisol.

These hormones influence metabolism, including fat tissue activity where FIAF is expressed. Metabolism is what makes the key UPEs.

Fasting, which boosts FIAF, is also tied to light cycles, think of how daylight affects feeding patterns. If biophotons reflect or amplify these light-driven processes at a cellular level, they might indirectly tweak FIAF production by signaling energy states or oxidative stress in cells. If you cannot burn fat you are more likely to be mentally ill.

My decentralized ideas have always been spot-on that this topic doesn’t need a scientist to spell it out in a paper, absorption/emission spectra are measurable, and biophoton emissions are detectable.

The gap isn’t in the physics; it’s in tying the specific wavelengths of biophotons (which vary by cell type and state) to FIAF’s exact optical profile in vivo. Still, if gut cells emit biophotons in, say, the 300-400 nm range, and FIAF absorbs there, the optical photonics interaction’s real, study or not. It is first principle thinking. It is obvious what they problem. It’s like saying water absorbs infrared; we don’t need a new experiment to prove it gets hot under sunlight. Biology acts like it does, but in physics they use theoretical physics and first principle thinking to make predictions when the experiments are not done or cannot be done.

youtube.com/watch?v=1F5cik…
Read 17 tweets
Oct 9
When matter experiences this topologic change do you know it become capable of emitting photons? In biology we call this UPEs. That is what does all the information transferring in life to keep you alive and kicking. Image
2. In astronomy and cosmology Spectroscopy is a form of remote sensing, meaning it allows scientists to determine the composition of an object without physically interacting with it. This is how we examine remote atoms in deep space.

How do we know what other worlds are made of? Planets we’ve never touched, stars we’ll never reach? By reading their light. Why can't quantum biologists realize the same opportunity exists in cells?Image
3. Quantum biology cannot yet apply the same spectroscopic "reading of light" as astronomy because cellular components are too small to be analyzed by light in the same way, and the inherent quantum effects within cells are not easily distinguishable from background noise in typical biological systems. They do not have photomultipliers small enough to sample UPEs yet.

Just because the technology is not available or studied means we should ignore the idea. Absense of evidence is not absence of effect. This is first principle thinking that is missing from most scientists today. In physics theoretical physicists provide a first principle lens to the Standard Model to innovate. We need to do the same in quantum biology. This is what I do.

Astronomers use spectroscopy to analyze the wavelengths of light absorbed or emitted by large celestial bodies, which reveal their chemical composition. However, cellular molecules are often too small to generate a detectable light signature, and the complex, noisy environment of a living cell makes it difficult to isolate and interpret the faint quantum signals associated with specific biological processes. there is no doubt today UPEs are real and carry information. We've know that AXIOMATICALLY since the Onion root experiment in 1922.Image
Read 16 tweets
Oct 8
Cutaneous antimicrobial effects of sunlight on cholesterol conversion to Vitamin D components are today's PSA boys and girls.

1,25(OH)2D made in the liver and kidneys from 25 D(OH) from the skin by the sun and cholesterol and its receptor regulate the processing of the long-chain glycosylceramides that are critical for the skin barrier formation which is crucial in defending the skin.

Do you know how the heme protein enzymes CYP control this process?

The two Vitamin D biomolecules induce toll-like receptor 2 (TLR2) and its coreceptor CD14, which initiate the innate immune response in the skin. Activation of these receptors leads to the induction of CYP27B1 (heme protein), which in turn induces cathelicidin resulting in the killing of invasive organisms.
What happens when blue light and nnEMF destroy heme proteins when you know this connection? Innate immunity is destroyed. This is why Fauci wanted you indoors during COVID he and Baric made in Ukraine and China. ncbi.nlm.nih.gov/pmc/articles/P…Image
2. See how the heme photoreceptors are blown away? Image
3. Spine tumors are not common but most of them are associated with a poorly functioning immune arm and associated with low Vitamin D levels from poor solar exposure. That is something you can prevent to avoid this outcome.
Read 7 tweets
Oct 8
Fire your centralized doctor by hiring nature for your reversal! Nature quantizes the precise amount of melatonin from the mitochondria needed to optimize autophagy and apoptosis. 95% of melatonin is made in human mitochondria. It is not your pineal or your gut. Your central retinal pathways have more mitochondrial density in it than any other part of the brain. The same is true with DHA to run your SCN faster than the other molecular clocks in your body to meet relativity needs. Want more info on exogenous melatonin? Use Yandex search with my name and mitohack #722. Your welcome in advance.Image
2. Shall we also say that sunlight plus natural darkness at night control melatonin, which in turn controls HIF-1a, which in turn controls sensing of O2?

Guess what happens to your mitochondria when oxygen tensions change? The IMJ geometry changes, metabolism morphs, geometry alters, and UPE become less common but more coherent. Mitochondria can change their physiology when the environment changes too. This is a remnant of the GOE when we had chronic hypoxia. this is why we innovated HIF1 and linked it to the PER clock genes.

Did you know UV light exposure raises oxygen tension in the venous plasma?

Guess what that all implies?

I know a lot more than any centralized MD or PhD about how we really operate.

ncbi.nlm.nih.gov/pubmed/20449875

Yes, light shapes life by sculpting your colony of mitochondria to make coherent UPEs to build longevity.Image
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3. Implications? With sunlight we have crafted our skin and SQ tissues to be able to breath through our skin since the GOE. That is what it means. Image
Read 5 tweets
Oct 6
If you have a T1D child you have a light problem. That light problem has manifested in your germ line.

If you're a Type 1 diabetic, by defintiion you have a chronic UVA and UVB deficiency and a chronic overdose of artificial blue light and nnEMF. It is also axiomatic.

Look at the chart below. T1D is almost nonexistent near the equator

This isn't a coincidence. Diabetes is a LIGHT story not a food one. pubmed.ncbi.nlm.nih.gov/18548227/Image
2. By around 20 weeks of pregnancy, a baby girl’s ovaries already contain every egg she will ever carry.
Which means that when your grandmother was pregnant with your mother, the cell that would one day help form you was already there.

Three generations, held in one body.
This isn’t folklore. It’s embryology.

Pregnancy is sometimes called a three-generation event: grandmother, mother, child, all sharing the same environment in a single moment. Scientists call it multigenerational exposure. I call transgeneration biology.Image
3. But biology makes it hard to imagine these things don’t matter. The oocytes that hold potential life are shaped by the whole soup of environment, and so are the children they become:
☀️ Light and circadian rhythm
🌊 Water quality
🥬 Nutrition and minerals
🌬 The air we breathe
💊 Medications and substances
💤 The quality of rest and sleep
💭 The emotions we carry
🧲 Electromagnetic fields and magnetism
🧪 Toxins and chemicals

Even mitochondria, not just “batteries” but regulators of repair, signalling, and survival, are passed down the maternal line. It is an unbroken inheritance that centralized medicine continues to ignore at your peril.

Three generations are intertwined in every pregnancy in humans.

Biology is carrying echoes of what came before, and the possibility of restoration.

Parents need to become conscious of these risks to eradicate these diseases. The transhumanists seem to know, why don't the normies?Image
Read 5 tweets

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