Dr. Jack Kruse

02/28/2026

This was my favorite paper EVER written on mitochodnria because it helped me understand the link between melanin and cristae alignment. For me, this solved the "C-value paradox" and the "Regulatory Conundrum" of human evolution.

The reason humans look, think, and operate so differently from chimps, despite sharing 98.8% of the same protein-coding genes, is not because we have different "parts." It is because we have a fundamentally different timing and energy distribution system. Cristae geometry is a fossil for how we did it using an ancient system. Melanin is a chiral chaotic polymer that absorbs all frequencies of light. It is capable of directly communicating with the IMJ sans the genetic metabolic machinery on the IMM.

The three divers who saved the EU from Chernobyl on May 4, 1986 are the HUMAN experiment buried in this paper. All three survived and never got radiation sickness. They did get radiation tans on their legs because of what they had to walk through to save Europe from the core melt down. Their survival meant that radiosynthesis has to have a way to lead to cristae alignment, even in humans.

The "radioactive tan" was the physical manifestation of the body rapidly deploying melanin to create a chiral, spin-selective shield. This allowed electrons to continue "tunneling" through the IMJ even as the delicate genetic machinery was being bombarded. Because this mechanism is driven by physics (CISS and semiconduction) rather than biology (transcription/translation), it is nearly instantaneous and incredibly "hardy."

It is the same reason we found out in the last decade that the Chernobyl fungi and arthropods grow faster in the fire, because they aren't fighting the radiation; they are "plugging into" it.

https://martinpicard.substack.com/p/discovering-how-mitochondria-communicate

02/27/2026

Improve your ability to think in a decentralized manner. This new podcast makes that case especially in the last 40 minutes. https://www.youtube.com/watch?v=DAjTEOIH8Ww

This podcast is a banger because it hits both decentralized networks in ways you've likely never considered.

Thinking is not IQ. When people talk about thinking, they make the mistake of thinking that people with high IQs think better. That’s not what I’m talking about. Most MD’s thinking is centralized and devoid of decentralization. I hate to break it to you, but unless you’re trying to get into Mensa, IQ tests don’t matter as much as we think they do. After a certain point, that’s not the type of knowledge or brainpower that makes you better at life, happier, or more successful. It’s a measure, sure, but a relatively useless one for surviving wisely in a manufactured world by globalists.

If you want to outsmart people more intelligent than you, temperament and life-long learning are more important than IQ. Become a lifelong learner and do it under the sun’s power and the sun’s absence during the night. This brain surgeon says everything works better and is more complex for the functioning of the human brain.

Mentor Sessions Ep. 054: Peter McCormack & Dr. Jack Kruse Fabian Society Exposed: History, Money, Power, & HealthWhat if a centuries-old Fabian Society plot ...

02/26/2026

There is a belief in the centralized clinical community that chronic GLP-1 agonist use creates a state of functional vagal withdrawal in those with autonomic stress that is causing stomach paralysis via vagal nerve dysfunction. This new blog covers this topic.

The drugs do not destroy the anatomy of the nerve like in a surgical vagotomy. But the belief is the nuclei that the vagus is connected to is overloaded with deuterium and this slows the action potentials in the vagus nerve to lead to non functioning.

GLP-1 receptors are located on the nodose ganglion (the sensory hub of the vagus nerve). When these drugs bind to these receptors, their mitochondria's IMJ fill with deuterium, and the KIE causes the nerve to send "fullness" signals to the brainstem, specifically the nucleus tractus solitarius (NTS).

Excessive deuterium in the IMJ flywheel leads to motor modulation of the vagus nerve. Instead of blocking vagal output, these drugs cause s deuterium poisoning of the IMJ causing a loss of coherence in the action potential. For example, they may inhibit the "cholinergic excitatory" pathway (which normally speeds up the stomach) or activate the "inhibitory NANC" pathway to slow gastric emptying. The more deuterium, the more atomic mass accumulates and cannot be released via exocrine function and the paralysis of the gut is the result.

The AC power grid has the same effect on vagal function. It causes the autonomic nerve system to allwo more deuterium into the matrix to destroy IMJ alignment which disrupts energy transformation.

Instead, the chemical signaling threshold is altered. If the drug is stopped, many patients find their motility returns, but for some, the "re-boot" of the vagal-stomach connection takes a very long time to offload the accumulated deuterium in the Nodose and Nucleus tractus solitarius, leading to permanent damage.

Get more from Dr. Jack Kruse on Patreon

02/25/2026

Become anti-social and unsupervised in Nature.

https://www.youtube.com/watch?v=NG98vFRYYSc

New podcast out.

If the environment in some way reduces the quantum yield, you better believe that it also reduces the quantum yield in the IMJ in your mitochondria. The net effect, in plain English: if you are living in a low quantum yield environment for any reason, you have to work harder/do more to be healthy because the IMJ is your time ledger and it never forgets. That is all. Carry on.

🔥 Episode 19! 🔥In this episode Karl Lentini speaks with neurosurgeon and health educator Jack Kruse MD. Dr. Kruse explains in scientific detail the bio-che...

02/24/2026

Today's PSA is a deep one. Once deuterium pollutes the matrix: OXPHOS fails: The motors are broken. Cataplerosis is unleashed: The cell stops trying to make ATP and starts dumping TCA intermediates (like citrate) to create lipids for new membranes (to replace the damaged ones). UPEs spike: The "friction" from deuterium in the nanomotors releases incoherent photons (UPEs), signaling to neighboring cells that the environment is toxic.

When you go down in scale to the matirx sizes at Angstroms, the KIE effect becomes massive because of the inverse square law. His biochemistry experts have zero clue about the biophysics of the system. This is the ultimate "blind spot" in modern centralized medicine. When you shift the perspective from bulk biochemistry to molecular scale biophysics, the Kinetic Isotope Effect (KIE) is no longer just a minor laboratory variable, it becomes the dominant force governing life or death at the mitochondrial level. In the mitochondrial matrix, we are dealing with distances between respiratory proteins often measured in 10–20 Angstroms.

The Power of the Gap: Because the probability of an electron or proton "tunneling" across a gap follows an exponential decay relative to the distance and the square root of the mass, even a 1-Angstrom shift in protein spacing (caused by nnEMF-induced swelling) can lead to a 100x or 1,000x decrease in tunneling efficiency.

Mass Matters: When you swap Protium (1) for Deuterium (2), in a vacuum, the Kinetic Isotope Effect (KIE) is roughly 6.5 in a vacuum, but in the highly constrained, liquid-crystalline environment of the mitochondrial matrix, the "effective" KIE can be much higher. The "Massive" Impact: Because of the inverse square law as it applies to electromagnetic interactions and the exponential nature of quantum tunneling, doubling the mass (1→2) at those tiny distances doesn't just "slow" the reaction; it essentially snaps the circuit. Most biochemists are trained to look at concentrations ( and ) in a "beaker" model. They assume the cell is a bag of floating enzymes where reactions happen by random collision.

The centrlaized Rockefeller biochemists miss the "Quantum Wire" Fixed Geometry: Life does not happen by random collision; it happens via coherent electron/proton transport along fixed topographical pathways (the Cytochromes).

Frequency Match: If the vibrational frequency of the C-H bond is "detuned" by the extra neutron in Deuterium, the resonance required for the electron to jump from Heme A to Heme B is lost. The "Silent" Variable: Since Deuterium looks "chemically" identical to Hydrogen in a standard blood test (it has the same number of electrons), biochemistry-based medicine treats them as interchangeable. They aren't.

Rockefeller's "biochemistry experts" are looking at the macro-symptoms (low Vitamin D), while I'm looking at the sub-atomic cause (Deuterium-induced tunneling failure).

: Look for 15 years I have tried to educate you. THIS IS THE LAST TIME. So pay attention. Your Rockefeller education beliefs are all FALSE. When dueterium leakage occurs into the matrix it stimulates cat...…

02/23/2026

Without Vitamin D3’s solar spark in your skin's cholesterol esters, the VDR falters on your IMM, unleashing cataplerosis in the TCA cycle, spiking electron transport, and disabling apoptosis. This is the root of cancer, autoimmune disorders, and obesity, where cells multiply like stars gone rogue, as gluconeogenesis studies in cancer cells confirm. Blocking the sun by any means is centralized medicine's madness. In disease states, you need massive solar experiences to quell the maladies to tap the remedies of Nature's recipes.

02/22/2026

Check out my latest article: THE BIOPHYSICS OF MENSTRUATION https://www.linkedin.com/pulse/biophysics-menstruation-jack-kruse-pkswe
Biophysics explains more about women's experiences than meets the eye. Speaking of the eye, this is where the story of menstruation begins, specifically in the SCN, or eye clock. Our eye clock is a flow meter of entropy, from a biophysical standpoint.

How UV Light "Un-jams" the System the system built to be costly in time. UV light exposure (specifically morning sunlight) is seen as the "reset" for this optical system. HOW?

Optical Pumping: UV light provides the initial energy to "prime" the electronic states of the VLC-PUFAs.

Scrubbing Deuterium: High-energy UV photons can facilitate the replacement of deuterium with protium in the mitochondrial matrix by increasing the flux of the respiratory chain. This "cleans" the metabolic water transformed at CCO.

Bazan’s Retinal Findings: Bazan showed that elovanoids (derived from VLC-PUFAs) are essential for protecting the retina from oxidative stress. In biophysics, this "protection" is actually the restoration of the UPE signaling field. Without these lipids, the retina cannot process light into the coherent signals the brain needs to regulate metabolism.

Summary of the My Decentralized Thesis Logic
The Antenna: Leptin Receptor (tuned to ~220 nm).
The Power Source: VLC-PUFAs (Bazan’s lipids) acting as UPE generators.
The Saboteur: Deuterium (jabs, drugs, supplements, & seed oils) which "muffles" the 220 nm emission.
The Repair: UV Light Exposure which re-energizes the pi-electron clouds and restores the biophotonic signal.
TIME IS YOUR GREATEST ENEMY IN OUR MODERN WORLD BECAUSE OF THE WAY OUR RETINA/SCN WAS BUILT BY EVOLUTION.

A lady asks me a question on my forum..

02/21/2026

How and humans evolved autoimmunity. An epic tale of evolutionary biology underpinned by biophysics. It uncloaks the modern day functional /allopathic medicine liars among the public. https://threadreaderapp.com/thread/2025228404698603975.html

Never forget that POMC is a gene on chromosome 2 that is translated by environmental UV light exposure and/or endogenous UV biophotons from metabolism.

The Bottom Line: Iodine is the "glue" that keeps the POMC-driven CLIP firewall intact into the MHC II binding grove electrostatically. When you block the sun, remove iodine, and replace it with halogens like Fluoride or Bromide from your water supply, the firewall evolution built into Chromsome 2 collapses, and the "open-source API" of the human gut (Zonulin) becomes a liability instead of an innovation.

02/20/2026

Life, and, in particular, its amazing diversity spanning more than 21 orders of magnitude in size, is the most complex physical system in the universe. In spite of this, biological systems obey a host of remarkably simple and systematic empirical scaling laws which relate how organismal features change with size over many orders of magnitude.

These include fundamental quantities like metabolic rate (the rate at which energy must be supplied in order to sustain an organism), time scales (such as lifespan and heart rate) and sizes (such as length of the aorta or height of a tree trunk). Muscle requires a higher metabolic rate to maintain, and this is another fundmental relationship hypertrophy breaks for human longevity.

It is a remarkable fact that all of these can be expressed as power law relationships with exponents that are simple multiples of 1 (e.g. ~, 3, 3). They appear to be valid for almost all forms of life, whether it be mammalian, avian, reptilian, unicellular or plant-like. Clearly the universal character of these "laws" is telling us something important about the way life is organized and the constraints under which it has evolved.

In my decentralized medical framework, the RPE-SCN-Leptin axis functions as a light-driven "clock-speed" regulator for the human metabolic engine, using melanopsin (OPN4) as the primary sensor to time-stamp energy production and storage. This makes all mammalian cells costly in time over energy.

02/19/2026

Appears my timing of dropping CPC #79 on Patreon was impeccable.

02/18/2026

Every single day you should wake up and commit yourself to becoming a better person. Here is my attempt for today.

Was my Ted Talk buried for the same reason Becker's lab was defunded?

This is the story of the 6 papers I received from the Qualcomm executive wife of an othorpedic surgeon and the book the Monk Who sold His Ferrari.

Strap in ----> https://www.patreon.com/posts/cpc-79-nazi-glp-150952073

In this massive blog, CPC #79 you will see why Epstein's interest in genetics led him to fund or socialize with Harvard scientists, where much of the HGP work occurred on finding weakensses in the human genome that could be exploited by BigHarma gain, including discussions on eugenics and gene editing. Why?

At 30 years old Epstein, was brought into the close circle of the Trilateral Commission, the CFR, and Rockefeller Family and told about the real purpose of the "Green Revolution" that they began in the 1950s under J. Richardson Dilworth. Dilworth transformed the Rockefeller family office (Room 5600) into a sophisticated BioTech investment engine and now Epstein was being groomed to do the same. Soon after understanding the plan, he began to host meetings at his New Mexico Zorro ranch (near Los Alamos National Laboratory, also involved in HGP) which aimed to "seed" humanity with his own DNA via genetic engineering to alter Chromosome number two on behalf of his benefactors.

The HGP (1990–2003) sequenced all chromosomes, with chr2 completed by a consortium led by Washington University. Gates' funding accelerated UW's contributions, creating economic value estimated at $800B from HGP advancements. I have believed since 2011 that the Rockefeller Epstein linkage was due to the Integration of what Gates found on Chromsome two after the Human Genome Project. This physical joining on the p-arm of human chromosome 2 created a unified "Control Center"for blood, light, and metabolic timing and the goal of the Rockefeller Dynasty has been to destroy it.

This is an epic history lesson for the ages on MKUTRLRA programming buried at the core of Rockefeller Medicine which created a killing machine for melanin destruction using GLP-1 agonists.

You won't be ready for this history lesson.

Get more from Dr. Jack Kruse on Patreon

02/16/2026

Today's PSA IS A DEEP ONE. https://threadreaderapp.com/thread/2023429542761644045.html

This thread references this pod below https://www.youtube.com/watch?v=y5DEQ1NpMN4&list=PLrv4qp8WwfQGaNjEb9YpEi_rIQfhWviIL&index=2

In this groundbreaking interview with Prof. Alistair Nunn, we discuss how modern humans are living in an environment radically different from the one our bio...