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.
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.
4. Environmental Sensing Through Water and IodineIodine's Role:
Iodine, concentrated in the thyroid, brain, and gut, plays a critical role in altering the hydrogen bonding network in water. It forms ionic liquids that enhance charge transport, protecting sensitive molecules like DHA from oxidation and facilitating rapid electron and proton movement. This is particularly important in neural synapses and CSF, where environmental signals are processed.
Sensory Systems:
The human body uses water's hydrogen bonding network to sense environmental signals through all five senses. The interaction of light with water in the brain, for example, converts environmental signals into electrical and then light signals, which are transmitted via white matter tracts. This process recapitulates environmental information within mitochondria.
5. Epigenetic and Disease Implications
Epigenetic Switches: Environmental factors, including light and temperature, can alter the hydrogen bonding network, affecting protein folding and epigenetic switches. For instance, changes in iodine levels or light polarization can lead to misfolded proteins and diseases like Multiple Sclerosis or autism, by disrupting the communication between mitochondria and the environment.
Disease States: Excessive light release from mitochondria or improper hydrogen bonding can lead to altered proton signals, affecting cellular communication and leading to disease. Cold thermogenesis, by increasing the magnetic force and condensing water, can restore proper communication by enhancing the hydrogen bonding network.
6. Mitochondria communicate with the environment directly through the hydrogen bonding network in water, which acts as a medium for energy and information transfer. This network is influenced by light, temperature, and the presence of ionized hydrogen and iodine, creating an ionic plasma that facilitates rapid proton and electron movement. The interaction of mitochondria with environmental electromagnetic fields, mediated by water and light, allows for the sensing and processing of external signals, ensuring that cellular processes align with environmental conditions. This complex dance of hydrogen, water, and light is fundamental to life and health, explaining how mitochondria act as environmental sensors within cells.
The MITO is the edge.
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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.
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.
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.
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.
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.
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.
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.
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?
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.
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.
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.
2. One of my members Johan of Norway wrote this and he got banned on X so I am posting his notes of the podcast for the Savages because I thought it was a good and accurate.
3. The rest is from Johan.......
Distinctions and Implications of Power Structures and Bitcoin as Resistance
Based on first-principles thinking and Dr. Jack Kruse’s perspective for "savages" (individuals prioritizing decentralization and sovereignty), this report outlines the distinctions between key power entities—bankers, Military-Industrial Complex (MIC), mafia, Mossad, CIA, Rome, Israel, Zionism, Jews, City of London, Royal Family, World Economic Forum (WEF), Fabians, and Council on Foreign Relations (CFR) and their implications for resisting centralized control. The analysis avoids centralized dogma or official narratives, focusing on Kruse’s ideas for decentralized survival.