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
Image
Image
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

Jul 3
Fasting and calorie restriction happens naturally via leptin melanocortin signaling and the effect of VDR on the IMM ECT. First principle thinking alone tells you that sunlight does this and lowers GDF15 mimicking calorie restriction. Avoiding Stress-Inducing Activities is also modulated by leptin melanocortin signaling by raising Parasympathetic signaling and controlling SNS. Sleep and recovery are increased by AM solar exposure. The sun is the best way to lower GDF15 and nothing approaches its success.
2. Leptin-melanocortin signaling can modulate autonomic nervous system activity, increasing parasympathetic tone and dampening SNS activity, which reduces stress responses like adrenaline release. GDF15 is upregulated by SNS activation (e.g., adrenaline-induced lipolysis in mice), so enhancing parasympathetic signaling could theoretically prevent GDF15 spikes.Image
3. Stress reduction via parasympathetic dominance (e.g., through relaxation or leptin-mediated hypothalamic effects) lowers GDF15 by avoiding stress-induced triggers. Reducing SNS activity aligns with reactions of GDF15 lowering to a decreased metabolic stress, decreasing GDF15, The SNS and the leptin-melanocortin pathway act in unison to lower chaos to improve signal fidelity.Image
Read 22 tweets
Jun 30
The Malate-Aspartate shuttle and its role in connecting cytoplasmic and mitochondrial NAD+/NADH pools are linked to sunrise effects on TCA cycle stoichiometry. This connection arises because circadian cues from sunlight can modulate TCA cycle intermediates (like malate), which the shuttle relies on to maintain NAD+/NADH balance across cellular compartments. NAD+ has a 258 nm absorption spectra and NADH is 340nm. LIGHT is a huge part missing in this story.Image
2. Ionized Hydrogen (H+) in Mitochondria

Proton Jump Conduction (Grotthuss Mechanism): Within mitochondria, H+ ions (protons) are abundant in the matrix. These protons can move rapidly through water via the Grotthuss mechanism, which involves quantum tunneling. This mechanism allows protons to hop through the hydrogen bonding network, effectively creating superconducting proton cables that facilitate rapid communication.

Ionic Plasma Formation: When hydrogen is ionized, it forms an ionic plasma that behaves like a liquid metal. This plasma, enhanced by iodine, enables efficient charge transport within mitochondria and other cellular fluids like cerebrospinal fluid (CSF). The presence of iodine in CSF, for instance, helps form these superconducting proton cables, linking mitochondrial function to environmental signals.
3. Light Excitation of Electrons:

Mitochondria release infrared light, which interacts with the surrounding water to charge separate it into H+ and OH⁻ ions. This light also excites electrons within the electron transport chain (ETC), influencing the redox state and energy transfer efficiency. The interaction of light with water and mitochondria is crucial for sensing environmental changes.

Magnetic and Electric Fields:

Mitochondria, due to their high density of H+ ions and the presence of transition metals in the ETC, generate strong electric and magnetic fields. These fields can interact with environmental electromagnetic forces, such as those from the ionosphere or solar radiation, to modulate mitochondrial function. The paramagnetic nature of oxygen further enhances this interaction, drawing it towards mitochondria.
Read 6 tweets
Jun 24
DNA's use of helical geometery seems to have a lot on common with the Cosmosi use of electric and mangetic flux in a Birkeland current's organization.

I'm drawing an intriguing parallel between DNA’s supercoiled, torsion-driven structure and the organization of a Birkeland current. Birkeland currents, observed in plasma physics (e.g., in space plasmas or auroras), are helical, twisted flows of charged particles guided by magnetic fields, carrying electric currents along twisted magnetic flux tubes. The sun does the same.

This similarity in helical geometry and energy storage is a fractal I have explored in many blogs. this is why polarization is a big deal. It is why sunglasses are a problem and this showed up in Becker's experiments on sleep.
The Sun and mitochondrial colony is connected in this way wirelessly.
Both systems rely on twist as a stabilizing and functional feature. DNA’s supercoiling stores mechanical torque (10-20 pN·nm) to regulate access and compact genetic material, while Birkeland currents use magnetic torsion to channel plasma and sustain current flow over vast distances.

In DNA, enzymes manage this torsion to control gene expression, akin to how magnetic fields guide and modulate the current in Birkeland structures. The idea of tension gradients in DNA mirrors the dynamic equilibrium of magnetic tension in Birkeland currents, where twist maintains coherence against chaotic dispersion.

Additionally, the role of structured water in DNA stabilization could parallel the plasma environment in Birkeland currents, where charged particles and fields interact to maintain structure.

Both systems suggest a self-organizing principle: DNA’s coil as a biological “engine” and Birkeland currents as a cosmic one, both leveraging geometry and torsion for energy management. While direct evidence linking the two is speculative, the shared physics of helical organization and torque-driven stability offers a fascinating conceptual overlap to explain how life connects to the fabric of the cosmos.Image
2. Everything in cells have a torsion. It is part of the AMO design inside of a cell which is another key to the mystery of the recipe of Nature. Torsion is the key regulator of energy tunneling: correct twist narrows the energy barrier, boosting tunnelling probability, while loose or damaged coils disrupt conduction. This is quantum control mediated by mechanical tension, measurable in experimental setups.Image
3. DNA’s selectivity is discriminating by wavelength, polarization, and direction which means it absorbs specific fields. When the right frequency hits, charge conduction increases, water layers shift, and genes unlock, pointing to field-gated biology.

This is why I have a problem with guys like Micheal Levin who say EMF is not a story in biology. This is pur bullshit.

Low-frequency EMFs can unwind or block access, while infrared from mitochondria restores torsional symmetry. Natural rhythms (Schumann, solar, circadian) serve as environmental tuning forks, influencing expression.

Chromatin loops and field-sensitive telomeres organize exposure, and gene expression becomes resonance matching, not just transcription.

Resonant coils store energy, transmit information, and respond to field alignment, mirroring DNA, which stores mechanical stress, converts torsion into access, and tunes to environmental signals. When aligned, this field-aware coil enables life to “speak fluently,” blending quantum biology with measurable physics at the edge of science.Image
Read 10 tweets
Jun 18
Air condition can ruin circadian control.
2. Circadian biology uses what three metrics to control it, Jack? Light, dark, and temperature.
Potential Problems of living with Air conditioning?

Here’s a comprehensive list of potential issues, grounded in circadian biology and general health impacts:

Circadian Rhythm Disruption
Mechanism: Circadian biology relies on temperature as a zeitgeber (time cue). The body expects a gradual drop in core body temperature at night to promote sleep onset and maintenance. AC can create an unnaturally cold environment, potentially desynchronizing this process.

Effects: Difficulty falling asleep or staying asleep.
Reduced sleep quality (less restorative deep and REM sleep).
Altered melatonin production, as temperature dysregulation, can interfere with the pineal gland’s response to darkness.

Severity: Moderate, especially with chronic exposure, as it can lead to long-term sleep debt and hormonal imbalances.
3. Respiratory Issues: Mechanism: AC units can dry out the air, reducing humidity to levels that irritate the respiratory tract. They may also circulate dust, mold, or allergens if not properly maintained.

Effects: Dry throat, nasal passages, or sinuses, leading to discomfort or infections like sinusitis.

Exacerbation of asthma or allergies due to cold, dry air, or poor air quality. Increased risk of respiratory infections, as cold air may weaken mucosal defenses.

Severity: Mild to severe, depending on pre-existing conditions (e.g., asthma) and AC maintenance.
Read 15 tweets
Jun 12
1. Debye potentials, also known as electric double layer (EDL) potentials, describe the electrical potential difference across a membrane due to the presence of ions in the surrounding electrolyte solution. This potential arises from the interaction between charged surfaces and ions in the solution, influencing the distribution of ions near the membrane. LNP raise the Debye potentials when they are charged. This means that LNPs are more likely to interact with cell potentials.

I have been studying vials of jabs from different countrie s to see if there was any chicanery done by the manufacturers of the jabs and I have found that the ones earmarked to Israel had neutral charges on their LNPs. Some states in the USA also showed this effect. (Vermont, Mass, NJ) I believe this is why these high compliant places did not have the side effects that other zip codes had due to Debye potentials.

Recall, that due to the presence of phosphate groups in nucleotides, DNA/RNA have a negatively charged charge. RNA contains a ribose sugar which is more reactive than DNA. DNA is a more stable molecule than RNA due to its deoxyribose sugar. It contains one less oxygen-containing hydroxyl group confering this ability.

DNA/RNA are dimagnetic. During mitosis when the nucleic acids are most at risk mitochondria undergo fragmentation and are redistributed throughout the cell. This process ensures that magnetic forces from the ATPase do not affect chromosomes separation. If this process is deffective due to LNPs charges, aneuploidy and alterations in microtubule function is possible. This is also critical time in the cell because mitochodnrial fragmentation allows each daughter cell to receive a sufficient number of functional mitochondria. Specifically, mitochondria lose their connections to microtubules, allowing them to distribute more evenly and avoid being trapped by the mitotic spindle. LNPs can interrupt this process. These effects would be seen in aftermarket data.
nature.com/articles/s4146…
2. Haplotypes influence uncoupling efficiency, which ties into mitochondrial processes and potentially ultraweak photon emissions (UPEs).

Here's how they connect: Haplotypes can affect the expression or function of proteins involved in the mitochondrial electron transport chain (ETC), such as cytochrome c oxidase (CCO, Complex IV). CCO plays a key role in oxygen reduction and water formation during ATP synthesis.

Variations in genes encoding CCO subunits or related regulatory proteins (e.g., due to haplotypes) alter uncoupling efficiency, where protons leak across the inner mitochondrial membrane, reducing ATP production but generating heat and reactive oxygen species (ROS).

This uncoupling therefore influence UPEs, since UPEs are thought to arise from ROS-mediated oxidation of lipids or proteins, a byproduct of mitochondrial metabolism.

Since CCO controls water creation metabolically by facilitating the final step of oxygen reduction (O₂ + 4H⁺ + 4e⁻ → 2H₂O), haplotype-driven changes in its efficiency should modulate ROS levels and, consequently, UPE intensity. Higher uncoupling might increase ROS, boosting UPEs, while efficient coupling might suppress them. This is why high latitude deaths were so high compared to equatorial deaths from COVID or the jab.Image
3. Regarding LNPs, if haplotypes affect CCO function and uncoupling, this would indirectly influence the cellular environment (e.g., ROS or pH) that LNPs encounter, potentially impacting their charge interactions or stability. This is why different zipcodes have different aftermarket data. I believe some of the data theft from 23andMe was used in GOF viral construction and in the creation of of LNPs and their charges. The direct charge on LNPs remains dictated by their lipid composition, but haplotypes will certainly affect it. I worry that the cabal used stolen data to build this bioweapon.

Regarding DDW, Pollack’s research on exclusion zone (EZ) water suggests that structured water near hydrophilic surfaces can develop a net negative charge due to the separation of charge, with positive ions excluded from the EZ. If DDW, with its lower deuterium content, enhances EZ water formation (as some of his studies imply through improved structuring), it could exhibit a net negative charge.

This charge would theoretically influence the electrostatic environment around LNPs, affecting their interaction with cell membranes or mitochondrial components, especially if haplotypes modulate CCO activity and water production.Image
Read 6 tweets
Jun 11
What food really does in us?

It creates an ocean inside of us like we had in the womb.

That ocean is a semiconductor along with the protein semiconductors it surrounds creates light called UPEs.

The size of the ocean is stochastically linked to the spectrum and amount of photons made by mtDNA, blood, and DNA/RNA. mRNA from spike ruins water production. It creates a desert the size of MARS inside of your cells and skull and this is why it causes the diseases it does.

If you see the AM sunrise you can then use the TCA and urea cycle. = you can make the heat sink required to make the highest quality UPEs your cell needs to do all the amazing things if does.

Complete combustion of 100 gms of

FATS = 110 = 110 gms of DDW from CCO
Protein = 75 = 75 gms of DDW from CCO
Carbs = 55 = 55 gms of DDW from CCO

nnEMF/blue light force use of all glycolysis and PPP because they force all Fe to the +3 state = your running hypoxic and on the oldest metabolic pathways from the GOE that were built for more non complex life. Life did not have a Ferrari engine in their skull that get 20% of Cardiac output which needs all its hemoglobin in the +2 to carry O2 to the mitochondria of the brain who wants to run the TCA and urea cycle. This is why the brain is covered in CSF = 99.8% DDW from choroid plexus which is an ultrafiltrate of your blood.Image
Image
Image
2. Darwin cannot explain 3 things we know are true today

1. Cambrian explosion

2. The transition from a chimp to human

3. Why do primates have the same number of genes as humans yet are so different?

A longstanding debate in evolutionary biology concerns whether species diverge gradually through time or by rapid punctuational bursts at the time of speciation. The theory of punctuated equilibrium states that evolutionary change is characterized by short periods of rapid evolution followed by longer periods of stasis in which no change occurs. Despite years of work seeking evidence for punctuational change in the fossil record, the theory remains contentious. This changed in September 2022 when genomic arrays of the clade of mammals were completed. What did it show?Image
Image
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3. The reason evolutionary biologists were impotent to find these answers in the fossil record was that melanin from the POMC gene explained these paradoxes and was highly conserved in DNA that was stable in the mammalian tree.

See that September 2022 paper here.

doi.org/10.1073/pnas.2…Image
Read 20 tweets

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