1. When inflammation is present in the brain (excess protons or too few electrons), the three fundamental laws of nature are altered in our tissues. This causes them to decrease their ability to deliver higher levels of oxygen to the neocortex below to maintain proper cognitive function. This decreased oxygen density over specific portions of the neocortex acts to limit its function, relative to other areas of the neocortex by changing proton conduction.
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2. This single event uncouples mitochondrion in the neocortex and it raises that neuron’s basal metabolic rate. A chronic raised basal metabolic rate leads to cerebrovascular diseases because it increases mitochondrial respiration and the amount of physiologic work a cell has to do. This is why ALL brain diseases are associated with atherosclerosis at a core level. This is precisely how leptin resistance causes a neuro-cognitive decline in humans.
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3. The CSF around the hypothalamus becomes less dense and has a higher temperature with higher levels of cytokines in it, causing us to lose energy/info to the environment. We’ve known for a long time that only two things lower metabolic rates in living things, strong solar stimulus, and cooling. This changes the hydrogen bonding network possible in CSF. The problem for medicine is that these scaling laws of energy flux have not made it into clinical medicine as yet. This loss of energy means less oxygen is delivered to the neurons in the hypothalamus, which is designed to work optimally when there is harmony and energy balance in humans.
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4. This is why in EMF 2, I told you the leptin receptor was an ‘account’ of photons, protons, and electrons. All bits of matter that make things up roughly have equal numbers of electrons and protons. The number of photons varies. The basics of what most people forget are that if this were not so, there would be an excess of a positive or negative charge, and this would create a massive force pushing all the excess charge out, leaving behind a core group of neutral charges.
5. When sunlight moves electrons/protons in us with the energy in light waves it alters the arrangement of our bio-molecules and changes their thermodynamics. A change in an arrangement is a change in the "information" in the system. Different molecular arrangements have different energies/information associated with them. This difference in energy/info is how bio-molecules are quantized to light frequencies. It also explains how metabolic networks became coupled to terrestrial solar frequencies.
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6. The brain evolved, I believe to order this process using solar frequencies between 250-780 nm. The circadian signals are how that energy harmony is translated from the outside world to the inner workings of biochemistry. When these signals are off for any reason at all, we begin to lose energy to our environment by emitting black box radiation from our bodies. Essentially, we are losing captured sunlight, and this decreases the amount of physiologic work a cell can do. This means in illness cells are losing energy at the vibrational or electronic level and can no longer remain a dissipative structure.

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7. Prigogine defined dissipative structures and their role in thermodynamic systems far from equilibrium, a discovery that won him the Nobel Prize in Chemistry in 1977. In summary, Ilya Prigogine discovered that the importation and dissipation of energy into chemical systems could result in the emergence of new structures (hence dissipative structures) due to internal self-reorganization. In his 1955 text, Prigogine drew connections between dissipative structures and the Rayleigh-Bénard instability, and the Turing mechanism.  Prigogine's theorem is germane to these ideas.

Mitochondria are dissipative structures in cells, but not the only ones.  They transform energy and create order from the disorder in light energy they use to operate.  The water mitochondria create is probably the single most important dissipative structure that life is based upon in cells.  According to Prigogine, determinism loses its explanatory power in the face of irreversibility and instability in dissipative systems. This is a major departure from the approach of Newton, Einstein, and Schrödinger, all of whom expressed their theories in terms of deterministic equations.
8. Indeterminism is the opposite of determinism and is related to chance.  Chance is related to probability. In science, most specifically quantum theory in physics links directly to probability and not cause and effect.  Indeterminism is the belief that no event is certain and the entire outcome of anything is probabilistic. Heisenberg's uncertainty principle and the "Born rule", proposed by Max Born, are often starting points in support of the indeterministic nature of the universe.  Indeterminism is also asserted by Sir Arthur Eddington and Murray Gell-Mann. Indeterminism has been promoted by the French biologist Jacques Monod's essay "Chance and Necessity". Ilya Prigogine argued for indeterminism in complex systems.
9. At life's genesis chaos has to gain order.  Dissipative structure theory really aims to solve this problem for biology by using physics.
Dissipative structure theory led to pioneering research in self-organizing systems, as well as philosophical inquiries into the formation of complexity on biological entities and the quest for a creative and irreversible role of time in the natural sciences.

There is a well-known theorem of minimum entropy production derived by Prigogine, which states that entropy exported from a system reaches a minimum, or becomes zero, at thermodynamic equilibrium and at steady states close to thermodynamic equilibrium. Prigogine's theorem is a direct consequence of Onsager's reciprocity relationship which holds at steady states close to thermodynamic equilibrium. The principle of internal entropy compensation, is in addition to, and implies the principle of minimum entropy production, and may even be valid in regimes far from thermodynamic equilibrium.
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10. He had some very interesting things to say about TIME in his work and Nobel Prize speech.  You should watch it sometime. I think they are key to understanding circadian biology and timing. All of our time reversible equations in physics created by Newton, Einstein, and Schrödinger describe a simplification of what actually occurs in nature. We live our lives with eyes blinkered, dismissing reality as the exception to our neatly formed approximations of what time really is.
11. Time is a critical issue for dissipative systems.  While most current thermodynamical analyses used in biology completely ignore space-time structure, the “thermodynamics of organized complexity” applying to living systems depends WHOLLY on space-time heterogeneity, which allows ‘free’ variation of microscopic states within macroscopic constraints.  THIS DEFINES WHAT A MITOCHONDRIA WAS DESIGNED TO DO AND TO BE IN A VARYING  EMF FIELD CREATED ON THIS PLANET by the sun.
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12. His theories offer us another possibility of some form of enthalpy-entropy compensation, as mentioned in my work in connection with enzyme catalysis, so that coherent energy is conserved in organelles in the cell, with no entropy generated. This is maintained by the atomic organization of atoms in a cell. The system could be arbitrarily far away from equilibrium, so long as, at some sufficiently macroscopic space-time of interest, the overall balance is attained, and the net entropy production of the system either vanishes or reaches a minimum.

The internal balance of entropy production means that the system maintains its organized heterogeneity or dynamic order. It is in turn dependent on energy flow being symmetrically coupled and cyclically closed over the system as a whole. In other words, it depends on the validity of Onsager's reciprocity relationship in systems far from thermodynamic equilibrium.
13. Circadian time stamping is done AFTER DNA is translated. This implies that the genetic code is not the primary issue in diseases and health creation. Time stamping is due to his theorems of Prigogine. Circadian time stamping also puts undue stress on our cell’s mitochondrion and they begin to act less like a part of our cellular design and more like a captured slave bacteria that they really are.  Since a mitochondrion has bacterial origins, most of man’s chronic diseases look like infectious diseases at the core.  This is deceptive because this viewpoint does not go down to the most critical level to understand how subatomic charged particles behave at small scales with the electromagnetic forces that light waves can impart to them.
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14. One of the hallmarks of the living system in cells is that they are exquisitely sensitive to specific, weak signals. Most of these signals are electromagnetic in nature. The human eye can detect single photons falling on the retina, which pass information directly to the SCN and all its mitochondria. This retina is where the light-sensitive photoreceptors in cells send out an action potential that represents a million-fold amplification of the energy in the photon. This defines what a non-linear stimulus is. Some of you know it by the butterfly effect.

It is not just a property of the central retinal pathways. The entire system is a plasma or syncytium of excitable matter ready to react to the environment's EMF signals. Similarly, a few molecules of pheromones in the air are sufficient to attract male insects to their mates. This sensitivity is characteristic of all parts of the system and is a consequence of the energy stored = related to the AMO physics of organization.

No part of the system has to be pushed or pulled into action, nor be subjected to mechanical regulation and control. Instead, coordinated action of all the parts depends on rapid intercommunication throughout the system because of how it is built to react to light. The organism is a system of “excitable media” (syncytium) — excitable cells and tissues poised to respond specifically and disproportionately to weak signals because a large amount of energy stored everywhere automatically amplifies weak signals. These signals often direct things in cells into macroscopic actions. This is how order is built from chaos in a dissipative structure described by Prigogine's theorem.
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15. Lesson over. Image

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More from @DrJackKruse

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
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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
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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
Jun 8
The "hard problem of consciousness," introduced by David Chalmers, refers to the challenge of explaining how physical processes in the brain give rise to conscious experience, the subjective "what it's like" aspect of mental states. When you are done with #55 I will have answered every question about it.

My ideas on consciousness will push boundaries over the precipice, because they offering a profound, elegant solution to the "hard problem"
patreon.com/posts/decentra…
Your World, Your Lens: You Don’t See Reality—You See What Serves You

In my manifesto, I believe, Decentralized Medicine #55 will go on the Pantheon of my top ten blogs. It might be the best one I have done because it answers questions no one has. My philopsophical transaction will shift your lens, by altering the light of UPE to change your world. You will see how consciousness was crafted by Nature and what a story it is for a Sunday AM.

What’s one thing you saw today that wasn’t what it seemed?

What’s shaping your reality today? Fear? Hope? Habit?

Your truth isn’t THE truth.

Ever wonder why you see what you see? Your mitochondria are talking, syncing light and energy to build your reality. What’s one moment today where your perception felt ‘off'?

You don’t see the world as it is—your consciousness, wired by mitochondrial motherboard and UPE-guided neural circuits, sculpts what’s useful. From Turing’s patterns to circadian rhythms, your brain’s electromagnetic roots shape your lens

Reaction-Diffusion Dynamics is the key theme in Turing’s model of morphogen gradients and this aligns with my version of how mitochondrial communication is done by electromagnetic signals. The blogs focus on mitochondrial specialization (e.g., functional diversity via quantum effects) mirrors Turing’s instability-driven patterning, where NCCs use mitochondrial UPEs and magnetic fields as morphogens to break symmetry and form brain structures (e.g., retina, cortex). Noether's and Shannon will make an appearance too.

Count on it.

Your reality? It’s coded by light and energy in your cells

Your World, Your Lens: Consciousness Shapes Reality—You See What Your Mind’s Wiring Allows.

Your Consciousness Isn’t Just You—It’s a Cosmic Circuit Board.

Your consciousness isn’t just ‘you’—it’s a mitochondrial symphony shaping your reality. What’s your lens showing you today?
2. Implications of this blog for people like @NicoleShanahan ?

My Photobiological Recursive Loop:
UPEs and Mitochondrial Activity: UPEs from Neural Crest Cells mitochondria couple with MT dynamics and circadian timing, driving mitosis and differentiation of sensory structures during neurulation. The embryo begins to focus on UPEs, which are crafted during early embryonic patterning (e.g., Wnt, FGF, BMP).

This suggests to me they are the signals may modulate UPE emission, aligning with your recursive loop. Why is it them? Because a normal embryo is 90% water. This tells me that Autism can be caused by the disruption of that three-peptide, which alters the recursive loop, or dehydration for any reason. This explains the epigenetic change in the number of affected boys from 1 in 100,000 to one in 12 boys in California.

Water and Coherence: Since the fetus is composed of approximately 90% water, which is structured into coherent domains (CDs) by UPEs, this directly enhances signal diffusion between NCCs and placodes. The photomolecular effect in water is expected to restructure water clusters, thereby optimizing sensory organ development.

Circadian Rhythms: The conserved GnRH2 and ipRGC-SCN axis (from placode/NCC contributions) link sensory development to circadian regulation, preparing the fetus for postnatal sensory integration. This is also why sex differences exist in firstborn male autists.Image
3. Turing’s Morphogenesis Paper

Reaction-Diffusion Dynamics: Turing’s model fits the neural plate border, where Wnt, FGF, and BMP gradients act as morphogens, breaking symmetry to specify NCC and placode fates. My photobioelectric morphogens (UPEs, magnetic fields) extend this, with NCCs using these signals to pattern the cranial sensory system.

Pattern Formation: The interplay between migratory NCCs and invaginating placodes mirrors Turing’s instability-driven patterns, with UPEs and electromagnetic fields guiding the spatial organization of the pituitary, eyes, nose, ears, and ganglia.Image
Read 28 tweets

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