1. Martin is getting very close to understanding Uncle Jack. It seems I may have underestimated Levin, too.
ERP and Post-K-T Survival
The K-T extinction, triggered by the asteroid impact 66 million years ago, created a high-stress environment with reduced sunlight, disrupted photosynthesis, and scarce food—conditions that would elevate éR across ecosystems.
Eutherian mammals and theropod dinosaurs (evolving into birds) survived by modulating éR through specific adaptations: Mitochondrial capacity and Melanin are ERP measures.
Mitochondrial Amplification:
Birds: Birds have amplified mitochondria in flight muscles and appetite centers to manage the high éR of sustained flight and foraging. This optimization minimized dissipative losses, allowing them to exploit distant, viable habitats.
Mammals: Enhanced mitochondrial activity around the hypothalamus (potentially for glucose synthesis from altered light) to regulate energy under low-resource conditions. This reduced éR spikes from starvation or cold, stabilizing their bioenergetic circuit.
Melanocyte Shift: The rising éR of the KT asteroid caused life forms who made it through the event to reject reptile and amphibian adaptation of chromatophores for the amplification of melanocytes. This was then tied to leptin-melanocortin pathways to make survival in a food-poor world possible for the early therapod dinosaurs and small mammals. This amplification and reliance of melanin due to altered light lowered éR by streamlining pigmentation energy costs. This shift supported UV protection and thermoregulation, key for endothermic stability, while avoiding the oxidative stress of older pigment systems.
Endothermy: As the most unappreciated metric, quantum-tuned endothermy allowed both clades to maintain a controlled éR baseline. By optimizing mitochondrial proton gradients and electron tunneling, they sustained metabolic work despite external chaos, counteracting entropy more effectively than ectotherms. Well done @MitoPsychoBio & @drmichaellevin
2. My discussion on the Tetragrammaton podcast with Andrew Huberman doves deep into the role of melanin in quantum processing, and my breakdown aligns with many of the concepts they explore while adding a quantum biological spin. Let me unpack how melanin amplifies quantum processing in mammals, mainly through electron surge, spin coherence, and energy bandwidth, and why this was a game-changer for Eutherian mammals and birds post-K-T event.
I’ll also tie this back to the Energy Resistance Principle (ERP) of Picard and Levin and then link it to the very unappreciated metric of quantum-tuned endothermy, while addressing the cellular impacts and evolutionary implications I’ve raised for 20 years
3. Melanin’s Role in Quantum Processing
As discussed in the podcast, melanin is a wide-bandgap semiconductor that absorbs light across a broad spectrum (all 73 octaves) far beyond chlorophyll’s narrow 400-700 nm range. This property allows melanin to harness light energy in ways that plants can’t, fundamentally altering how animals process energy and information at a quantum level. This would have been highly adaptive when the sun was blocked because of how chlorophyll operates with sunlight to create all the food webs. In evolution, chlorophyll came first, then hemoglobin, and then the KT event amplified melanin biology when the sun was dimmed.
4. Electron Surge
In the classical mitochondrial electron transport chain (ETC), electrons from food (via NADH and FADH₂) fuel a cascade that generates a proton gradient (ΔµH⁺) for ATP synthesis. As I've noted, this yields about 4-10 electrons per glucose molecule, a process well-documented in bioenergetics literature like Nicholls’ Bioenergetics (2013).
However, melanin introduces a quantum leap by splitting water (H₂O → 2H⁺ + ½O₂ + 2e⁻) under light exposure, a phenomenon I call “human photosynthesis.” This reaction, driven by UV and visible light (200-700 nm), generates a flood of electrons—potentially 10x more than chlorophyll’s output in plants.
5. This electron surge supercharges the ETC:
Complex I Overdrive: The influx of electrons from melanin-driven water splitting overwhelms Complex I, ramping up proton pumping into the mitochondrial matrix. If the matrix typically handles 10⁸ protons, this could scale significantly, densifying the proton gradient during the KT event.
Entanglement Scaling: The increased proton (H⁺) density enhances spin entanglement, a concept I have referenced with Binder’s work (2015). Protons, with their ½ spin, form a quantum network where entanglement scales as √N (where N is the number of particles). More electrons and protons mean a denser spin network, potentially accelerating quantum processing from linear to exponential rates.
6. Spin Coherence
Del Giudice’s coherent domains (CDs), as you mentioned, are regions in water where H⁺ spins align due to quantum electrodynamics (QED) effects, creating a “super-coherent” state.
In the podcast, I emphasized how melanin in the retinal pigment epithelium (RPE) and skin absorbs light, splitting water and generating H⁺ spins that align across these CDs.
Unlike the food-driven pathway, which relies on a slower electron trickle, melanin’s full-spectrum absorption (UV to IR) sharpens spin coherence. This move was all about taking full advantage of light when it became rare and scarce. This is what drives change. Why? Shannon 1948 paper: For a signal to have meaning, it must be rare or unusual.
7. How do we sharpen spin coherence?
Light Tuning: Visible light (532 nm, via the photomolecular effect) and UV (4 eV) excite melanin, aligning H⁺ spins more tightly. Del Giudice’s work (1988) suggests that such coherence extends NMR relaxation times (T₁), reducing decoherence.
Exclusion Zone (EZ) Synergy: Pollack’s EZ water, often static, shields CDs from environmental noise, but melanin adds dynamic spin-spin coupling (J-coupling), amplifying coherence across cellular scales.
Melanin’s semiconductor properties—its chaotic electron delocalization—mirror CDs, creating a quantum network that processes information faster and more robustly.
8. Energy Bandwidth
Mitochondria traditionally operate within a narrow energy bandwidth (250-780 nm), with cytochrome c oxidase absorbing 650-950 nm to drive proton pumping.
Melanin obliterates this limitation:
Broad-Spectrum Absorption: From IR (1 eV) to UV (6 eV), melanin captures energy across a continuous spectrum, eliminating the bandgap constraints of chlorophyll or even mitochondrial enzymes. This floods the ETC with electrons and biophotons (200-350 nm, as noted by van Wijk, 2014), which act as signaling molecules.
Quantum Processing Leap: The entangled H⁺ spins, now operating across a wider frequency range, enhance ATP synthesis (via F₀ torque in ATP synthase) and enrich redox signaling (e.g., ROS-driven pathways like NF-κB). This broader bandwidth allows cells to process energy and information simultaneously, a quantum advantage over food-only systems. you are now entering Uncle Jack's world where LIGHT is great than food and why Leptin Rx works.
9. Cellular Impact: The Quantum Leap for Mammals
Melanin’s amplification of quantum processing had profound cellular and evolutionary impacts, especially for mammals and birds post-K-T event:
Mitochondrial Battery: The increased H⁺ density from melanin’s water splitting packs the mitochondrial matrix, scaling entanglement density. If a typical cell manages trillions of quantum interactions, melanin could push this to quadrillions, as I've suggested. The piezoelectric effect on ATP synthase (F₀ torque) amplifies, generating higher voltages and faster charge cycles—light-driven, not food-lagged.
10. What else was optimized?
Coherent Domains: Melanin’s electron flood synchronizes water oscillations in CDs, tightening spin-spin coupling. Visible light (2-3 eV) splits water, while IR (1 eV) tunes CD oscillations, creating a multi-scale quantum processor from mitochondria to neurons.
Cell Signaling: Biophotons from melanin’s UV burst (200-350 nm) enhance signaling depth, following Fermat’s law as refractive indices shift in cellular media. Spin-driven redox pathways (e.g., NF-κB) and circadian clocks (via cryptochromes, CRY) synchronize, turning energy into information with unprecedented speed and reach.
Life was introduced to the dissipative state where it was 4 standard deviations over where reptile were before who kept melanin just on their interiors. Mammals put it everywhere.
11. Why Melanin Changed Everything
Chlorophyll locks plants into a visible-spectrum niche, relying on mitochondria to process leftovers. As I have highlighted for 20 years now, melanin lets animals harness all light that comes to Earth 24/7, turning H₂O into an electron and proton geyser. This explosion of cells' quantum capacity enabled mammals and birds to survive the K-T event.
Post-K-T Advantage: With sunlight dimmed by impact dust, melanin allowed these clades to generate their light (biophotons) and energy, decoupling them from photosynthesis-dependent food chains. Their mitochondrial capacity, amplified by melanin, sustained endothermy and flight (birds) or metabolic flexibility (mammals).
Quantum-Tuned Endothermy: Tying this to the ERP, melanin lowered éR by optimizing energy transformation. The electron surge reduced dissipative losses, while spin coherence minimized oxidative stress, allowing these animals to maintain metabolic stability in chaos.
Cultural Context: My reference to “Anubians at 28°N” suggests ancient humans in sun-rich regions (e.g., Egypt) maximized melanin’s potential, their mitochondria “singing” with quantum efficiency. Modern humans, in “LED caves,” just like the elite of Egypt buried in the gold sarcophagus disrupt this with blue light, stalling quantum processing and elevating éR—leading to disease, as the ERP predicts.
12. Melanin as Life’s Regenerative Current
My nod to Robert O. Becker’s regenerative current aligns with Kruse’s emphasis on light as life’s driver. Melanin’s ability to “hydrate melanin to dampen the ampere” (modulate electron flow) mirrors Becker’s DC currents in regeneration. Del Giudice’s QED framework supports this: melanin’s electromagnetic chaos entangles CDs, outstripping Pollack’s static EZ water or Chaplin’s non-spin clusters.
Life, as I say, is a “quantum dance of light,” and melanin orchestrates it, bringing mammals back from the brink of extinction.
13. LESSON OVER
14. Extra credit: Why is grass that undergoes slow decay always greener? Because anything green reflects green light and absorbs tons of blue and red and becomes more energy efficient because éR in the ETC of the grass is channeled to useful work and not lost by the plant. This insight is why I came to rationale to patients in January 2020 at the beginning of COVID to use MB to combat DARPA's COVID.
MB is blue and as such anyplace it flows will rejec the absorbtion of blue light. This means mtDNA would absorb more UV because MB increases NAD+ to do just that at 340 nm. It also would force more red light absorbtion at the Q cycle and cytochrome C oxidase to help the ATPase spin and the Q cycle deliever electrons to cytochrome C oxidase to keep cardiolipin damage at bay. The reason I knew hospitals would kill millions is because with COVID hypoxia they would default to oxygen therapy which would make the electrical resistance drops in ECT when oxygen is added due to its electronegativity. None of my ICU collegues listened to me but as soon as I started pushing MB when they left shift their patients got better. Vitamin C will do the same but MB is way better at the process.
MB and Mitochondrial Resistance: MB, by oxidizing NADH to NAD+,this influences the ETC (step 7). By increasing NAD+ availability, MB reduces the "load" on Complex I, effectively lowering resistance to electron flow and boosting ETC efficiency. This helps maintain the proton gradient (ΔμH⁺, step 8) and ATP production (step 9), counteracting mitochondrial dysfunction.
Melanin and Tissue Resistance: Melanin, a dark semiconductive pigment, contributes to tissue-level resistance by facilitating electron transfer in response to light. If melanin is dehydrated or absent, tissue resistance might drop (oxygen problem = ARDS), disrupting energy flow. MB compensates for these effects by acting as an alternative electron carrier, effectively increasing resistance in a controlled way to restore proper energy transformation.
Deuterium and Resistance: I've also mentioned for 20 yrs that deuterium’s impact on the NADH/NAD+ couple, which slows ETC speeds and disrupts the Q-cycle. Deuterium increases resistance in a detrimental way by slowing electron transfer (step 7). MB, by promoting NAD+ production with H⁺ (not deuterium), reduces this aberrant resistance, restoring efficient energy flow. MB can affect the spin effect of the extra neutron in deuterium. This is why it works in cancer too.
Neurosurgeons who do a ton of trauma cases know MB it modulates éR in the ETC to ensure energy is directed into useful work (ATP synthesis) rather than being lost as heat or ROS. If you remember the podcast with @JonesDanny and I talked about the one neurosurgery case that changed my life, the little girl I operated on all night during @Metallica 24 playlist, I had MB running in most of the night as I worked to remove the bone from her brain.
I was worried about this 16 yr old being able to recover from these injuries so I went peddle to the metal on MB. Way outside the package insert. Why?
MB use has broader implications: Resistance in Distributed Biological Systems
I knew that her neural, vascular, and other anatomical networks distribute and transform energy into information by varying resistance regions (éR) across massively distributed membrane systems working in parallel alignment. My profound insight that night almost got me fired when I told my staff doctor to get the fuck out of the room. Why did I go all in?
Neural Networks: The brain’s parallel processing relies on varying resistance across billions of neurons and synapses. This allows energy (ion gradients, bioelectricity) to be transformed into information (thought, memory, behavior). I wanted to perserve as much of her cognition as I could as I worked. This was the same idea I had on Rick Rubin for his open hear t surgery. Peter Attia told Rick I was nuts but Rick has that little girl to thank for the advice I gave his Stanford surgeon. The surgeon did not take it, but Rick did. He trusted me. Now the Famous Attia knows something he did not before. Not surprising since he never finished a residency so his clinical skills are not what they could be.
Vascular Networks: The circulatory system uses resistance to compute how to distribute energy (oxygen, nutrients). For example, during hypoxia (as in COVID-19), resistance in pulmonary vessels increases to redirect blood to better-oxygenated lung regions (a process called hypoxic pulmonary vasoconstriction).
Cellular Networks: Mitochondria within cells form networks that dynamically adjust resistance based on energy demand. For instance, during high ATP demand, resistance in the ETC decreases to speed up electron flow, while during low demand, resistance increases to prevent ROS production. Preserving Ricks cochlea from ROS damage was key in my recs to him on bypass.
In all these systems, resistance isn’t static—it’s a dynamic variable (éR) that organisms adjust to direct energy flow and process information. This mirrors how microcircuits use resistors to control current and perform computations. Seems like MB effects are well known by mitochodnriacs. I wonder why? ;)
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@MaxGulhaneMD I do have to say after the first 20 minutes I like the discussion but I was frustrated in spots where he was physics facile as he could have been but it is clear Nunn believes as I do that biology is not fundamental it is biophysical.
He is too much in love with Levin. Levin has do nothing to advance Becker.
But I want to tell you at the 1:10 mark you bring up CCO and DDW. Nunn seems uncomfortable.
He goes on to talk KIE boilerplate but he is a biochemist and is dabbling in biphysics so you need to push and extend him further on the D/H+ isotope selection process tied to photosynethesis creation of deuterium on the carbon backbone. there has to be a way to sort the isoptopes and there is biophysically but I do not think he knows what it is.
DDW, heat, and UPEs are exhaust products from matrix operation. He seems to know this. But so is CO2. He does not seem to know the biophysics of CO2 and its real purpose.
The Failure of Centralized "Exhaust" Logic is always on display with Nunn here.
Centralized medicine tries to "fix" CO₂ levels or pH chemically, failing to realize they are tweaking the isotopic selection process that uses magnetic tuning of a quantum circuit.
High CO₂ isn't just "acidosis"; it is the cell trying to increase its "Hash Power" and protect its internal water from the "Double-Spend" attack of entropy I describe in my thesis. CO2 is dimagnetic. this means it shields CCO from the magentic fields of the matrix. Ask yourself why? The answer is simple biophysics. It guarantees that H+ is pushed into the intermembrane space so the ATPase has it to use to spin the Fo head. Deuterium has a different magnetic moment so CO2 acts to sort it and keep it away from the Intermembrane space so that the nanotorque engine is not slowed or destroyed. Neither, Nunn, Boros or Somylai know this because they are blinded by biochemical BS.
So because you asked the question he could not answer he is the answer:
The Physics: CO₂ is highly diamagnetic. By concentrating it at the site of water creation (CCO), the cell creates a FOCAL magnetic "quiet zone."
The DC Current: This allows the protons (H+ not D) to flow in a coherent DC current of repair without being scattered by the "vibrational noise" of the environment.
The VDR Link to the shied: The VDR sitting on the IMM acts as the sensor that ensures the CO₂/O₂/Light ratio is tuned to keep this magnetic "shield" active.
VDR: The Photonic Antenna that directs electron flow, speed, and tunneling efficiency before cytochrome C
Fe-S/CCO: The Quantum Engine is the engine that allows electron and proton tunneling
Carbonic Anhydrase in the matrix/CO₂: The Magnetic Shield/Tuner selects the stochiomtery H+ inside the intermembrane space to deliver to the ATPase.
This mechanism is sorting engines into "good/health/CCO and bad/Disease/Cardiolipin/heteroplasmy to get rid of the bad via Cardiolipin, or to extend life with DDW from CCO to hydrate all our semiconductive proteins. Timing from the OUTSIDE environment photonic signals controls this process max. Recall how Vitamin D, Melanin, DDW, NO, and CO2 are all made. Outside in, not inside out. Biochemists always have the inside out framework because this is where biochemistry occurs. Outside in is where biophysics of life begins.
The Calcium-Melanin Nexus: Macro vs. Micro Control
My thesis identification of melanin's macroscopic chelation vs. Vitamin D’s stochastic sorting provides a complete picture of cellular calcium management:
Melanin (The Macro-Buffer): Melanin acts as a high-capacity reservoir that absorbs and stores calcium. Certain light frequencies allow its release. Vitamin D made from 312-320 nm exogenous light on cholesterol esters is sent inside to the kidney and liver for final processing. This binds the VDR on the IMM and it is the VDR that can get into the nucleus to alter it way after the photonics of this axis acts first with clock genes.
This "macroscopic chelation" of melanin provides a stabilizing background, preventing the "vibrational noise" of the environment from immediately overwhelming the cell's delicate electric circuits.
Vitamin D/VDR (The Stochastic Sorter): Sitting on the Inner Mitochondrial Membrane (IMM), the VDR acts as the "fine-tooth comb." It performs stochastic sorting, precisely directing individual Ca²⁺ ions to the TCA cycle dehydrogenases to tune the "Hash Power" (metabolic flux) based on the UVB/IR signals received from the exterior. VDR binding isolates CCO with CL.
The 30 Million Volt Charge: This charge on the IMM is the physical manifestation of the DC current of repair. It encodes photonic information as a voltage gradient, allowing the matrix to "read" the external environment through the language of electron and proton tunneling.
2. Other point @MaxGulhaneMD more for you than him. He does not seem to understand an additional neutron = more mass and as mass goes up what does Ilya theory from his Nobel in 1977 say? Timing slows.
So any additional mass irrespecitve of a KIE means that heteroplasmy expands because in CCO you have the story of life and death. A lot of H+ = CCO makes water and CO2.
Too much D+ and it stimulates Cardiolipin. Boros keeps confusing you with broken engines. They do not break. D+ cannot fit in the channel. The ATPase starves and the matrix swells and this stimulates forced apoptosis.
Decentralized Internal light Medicine done by the non visual photoreceptors is "Tuning the Shield"
The VDR, the Fe-S clusters, and the Carbonic Anhydrase system form a Triad of Temporal Control distally to the RPE-SCN.
The CO₂ Diamagnetic Shield
In my model, CO₂ provides the low-entropy environment required for the Protonic Spin-Ice (EZ water) to form. If you look at proton tunneling it is best modelled in ice. What these biochemistry guy don't yet relaize is when melanin is hydrated by DDW you create massive proton tunneling and you open more of the biophysics Pandora box like Grotthaus etcs........
3. The Solar vs. nnEMF Split: "Quantized" ROS
My slide below highlights the critical difference in how the cell processes Solar EMF vs. nnEMF (5G/Malware):
Solar EMF (Quantized Information): Sunlight creates a highly specific and sensitive amount of Reactive Oxygen Species (ROS). This is not "damage"; it is quantized information delivered via UVA/Blue light-stimulated Nitric Oxide (NO).
The NO Filter: UVA light controls NO production, which reversibly inhibits Cytochrome c Oxidase (CCO). This acts as a frequency filter for the DC current, preventing the "Double-Spend" entropy attack.
nnEMF Malware (Non-Quantized Noise): Unlike the sun, 5G/nnEMF acts as a Voltage-Gated Calcium Channel (VGCC) disruptor. This causes a massive, non-quantized "leak" of Ca²⁺, leading to:Hydroxyl Radical Flood: The resulting Fenton chemistry creates Hydroxyl Radicals (the most destructive ROS).
Photoreceptor Destruction: This noise "blinds" the internal lighting system of the non visual photoreceptors, leading to mitophagy failure and broken apoptosis, leaving behind a "static colony of defective mitochondria" (the hallmark of chronic disease/cancer).
Sorry @MaxGulhaneMD but I chuckled so hard listening to th first 20 minutes of this. When is this guy going to realize that Dr. Pirogine theory on dissipative structures has at its core a TIME SYMMETRY aspect. He still does not get it. Even at the Guy foundation they fly blind.
At life's genesis because of dissipative theory energy was always a commodity, but Time is the real value. He has no idea about the implications of this.
Evolution of life happens because life costly in time, not in energy because of the equations link to entropy.
this idea scales from stars to cells. A supernova has massive energy flux, but it is a state of total chaos (High Entropy). A human brain has much lower energy flux but evolved to have massive Temporal Coherence.
Each "event" in a cell, like a proton tunneling through a molybdenum transistor enzyme in mitochondria or a biophoton hitting a melanin sheet, is a "Block" in the ledger. It’s not "good" or "bad"; it’s a physical State Transition. Wisdom is the ability of the organism to maintain that ledger’s integrity against the "Double-Spend" attack of entropy. Sorry your expert fell short because he is ignorant about the 1977 Nobel Prize implication for mammals. youtube.com/watch?v=y5DEQ1…
2. Life is costly in time not energy goes right back to the 1977 Noble Prize. 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.
He had some very interesting things to say about TIME in his work and Nobel Prize speech. 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.
3. Prigogine’s work on Minimum Entropy Production explains why mammals must be "Costly in Time & not in Energy".
By proving that Time is Irreversible, he effectively "Hard Forked" biology away from the time-reversible approximations of Newton and Einstein. Time reversibility is built into the matrix. That is heteroplasmy. As it changes so does time you experience.
Near equilibrium, entropy production is minimized. But life exists far from equilibrium, much to the dismay of all your food guru friends. To maintain complexity, the organism must "export" entropy. This is why life innovated clock genes quick. They are flow meters for entropy.
My historical and political analyses have compared
the QAnon phenomena before DJT presidency (45th) and the 1920s Soviet counterintelligence operation "Operation Trust" (Operatsiya Trest) due to their shared use of psychological manipulation to pacify political opposition. If you review my twitter feed you'll see no QAnon posts because I believed they were counter ops of the Zionist controling Israel at this time. Bibi was that leader. He was reaching back into the Zionist bag to the take over of Russia in 1917.
The parallels between these two movements typically center on the following tactics:
"Trust the Plan" Narrative of 4D chess: Both movements relied on the central premise that a secret group of high-ranking insiders, patriots within the government or military, was working covertly to dismantle the regime from within.
Neutralization of Dissent: Operation Trust was designed by the Soviet secret police (Cheka/GPU) to create a fake anti-Bolshevik resistance (the Monarchist Union of Central Russia). Its primary goal was to convince opponents to wait for this "internal coup" rather than taking active measures, effectively stalling real resistance.
Discrediting Opposition: When Operation Trust was exposed in 1927, it humiliated those who had believed in it, making them appear foolish and reducing their willingness to support future anti-Bolshevik efforts.
Luring and Identifying Targets: Just as QAnon encouraged followers to identify themselves online, Operation Trust lured high-profile dissidents like Sidney Reilly and Boris Savinkov back to Russia, where they were captured or executed.
QAnon was part of the plan to turn MAGA to MIGA, in my opinion. The same thing that went on in Russia in 1917 is ongoing in Washington DC.
2. Palantir surveillance will be used to target those who went against this coup and they will be taken care of by the zionist faction that wins this coup between the bankers and transhumanist tech bros.
3. Point three as proof of the current coup of America by MIGA:
You missed a big lesson. The "Green Revolution" Pipeline of the 1940-2025 = Melanin Erasure Program
The Rockefeller/Monsanto/Sperry Rand trinity wasn't just about "feeding the world"; it was about standardizing the human bio-frequency.
The Inputs: Rockefeller provided the "seeds," Monsanto provided the "chemical metal-shredder" (Roundup), and Sperry Rand provided the "computational logistics" to scale this melanin-destroying diet globally.
The DARPA Connection: By canceling Robert O. Becker’s lab, DARPA protected this industrial model. They couldn't allow the world to know that we are DC bio-electric organisms whose health depends on the semiconductive fidelity of the melanin that the Green Revolution was designed to erase.
2. Room 5600: The Professionalization of Biotech Warfare
J. Richardson Dilworth was the architect of the financial "Pivot." He shifted the Rockefeller "Room 5600" from 19th-century industrialism to 21st-century Biotech Control.
The Venrock Ecosystem: By seeding Amgen and its peers, the family office created a "Multi-Client" trap. They funded the discovery of Leptin (1994) specifically because they already knew from the DARPA MKULTRA program that melanin was the key target to hit in farming. Glyphosate is a competive inhibitor of melanin. Few know it.
The Shelved the Leptin Trials: When the leptin trials showed that Light and Cold were the actual regulators of the pathway, they couldn't commercialize that, because there’s no profit in the Sun. So, they shelved the "Photonic" truth and pivoted to the Distal pathway below photonics and elevated the GLP-1 Agonists to treat the symptoms of the light-starved world they built in the 1960's BigTech revolution in Silicon Valley. Steve Jobs links to Rockefeller and Rothschild is deep.
The connection between Steve Jobs and the Rockefeller and Rothschild families is primarily rooted inearly-stage venture capital, shared high-level board memberships, and modern institutional investment. While Jobs was an adopted child of a working-class couple, his career in Silicon Valley was deeply intertwined with the financial infrastructure established by these dynasties.
The Rockefeller family’s venture capital arm, Venrock Associates, was one of the early investors in Apple Computer during its start-up phase in Silicon Valley. This initial capital was crucial for transitioning Apple from a hobbyist project into a scalable corporation. Venrock's involvement established a direct link between the Rockefeller family office (established in 1882) and the nascent personal computing industry.
The Rothschild family has maintained a significant financial interest in Apple through various investment vehicles:Rothschild Investment Corp: This firm identifies Apple Inc. (AAPL) as one of its top holdings in recent SEC filings.
RIT Capital Partners: Chaired by Lord Jacob Rothschild, this London-listed trust acquired a 37% stake in Rockefeller Financial Services in 2012, formally uniting the two dynasties' wealth management interests.
Laurene Powell Jobs, Steve Jobs’ widow, serves as a bridge to the elite policy circles traditionally associated with the Rockefellers:Council on Foreign Relations (CFR): Laurene Powell Jobs serves on the board of the CFR, an organization famously chaired by David Rockefeller from 1970 to 1985.
Ford Foundation: She also sits on the board of the Ford Foundation, another pillar of the philanthropic network where the Rockefeller influence is historically substantial
Jobs is often compared to John D. Rockefeller in terms of his business impact. While Rockefeller revolutionized industry through vertical integration, Jobs transformed technology through a closed ecosystem that redefined global consumer behavior = Why the Epstein emails call Jobs brilliant. Jobs and John D. Rockefeller integrated their business just like Groves did in the Manhattan Project. Go re listen to my Podcast with Breedlove on Groves.
Few can rival my research. I am all over these fuckers.
3. The Savage's Survival Guide
The "Centralized PhDs" are merely the maintenance crew for the Rockefeller/Amgen/Monsanto grid. They are trained to ignore the RPE-SCN-POMC circuitry because acknowledging it would dismantle the entire $100 million "Leptin Bounty" and the trillion-dollar pharmaceutical "Distal Patch" industry.
Uncle Jack, the warning to the Savages is clear:
Glyphosate is a "Metal Leaking" agent.
Blue Light is a "Timing Shredding agent."
Leptin Resistance is a "Power Outage" signal.
The Monk must not only sell his Ferrari; he must burn the Rockefeller "Roadmap" and reconnect to the DC Bio-Electric Current of the Sun.
How do we begin the "Melanin Reclamation" for the Savages who are currently trapped in the Green Revolution/Agenda 2030 isotopic sink?
Why doesn't Rockefeller centralized medicine work for 99.9% of people?
It is designed to make the family customers not deliver cures for the people.
This is why in Norway right now, below your ability to know it, because zionist media is quiet on it while they feed you Bondi nonsense (circus maximus), they are ransacking the house of the Nobel Committee leader. Jagland. LOL... bastards... Norway the perfect country for corruption.
This is why Epstein was at Harvard and MIT and why Maxwell family controlled PEER review in centralized science. It is why Robert O. Becker was cancelled by the front people (Dr. Phillip Hnadler) for Rockefeller Medicine. The entire scheme was designed to keep Rockefeller medicine in power. Few. Eric Weinstein wants to know why Epstein was in his math dept at MIT. This is why. Control the scientific narratives, control what gets funded and published, control what gets studied and what get buried to Pubsmear (Elisabeth Bik) and then you auction off Nobel Prizes and give them to researchers whose science leads to no cures.
@Kevin_McKernan @JesslovesMJK
2. Why doesn't Rockefeller centralized medicine work for 99.9% of people?
It is designed to make the family customers not deliver cures for the people.
This is why in Norway right now, below your ability to know it, because zionist media is quiet on it while they feed you Bondi nonsense (circus maximus), they are ransacking the house of the Nobel Committee leader. Jagland. LOL... bastards... Norway the perfect country for corruption.
This is why Epstein was at Harvard and MIT and why Maxwell family controlled PEER review in centralized science. It is why Robert O. Becker was cancelled by the front people (Dr. Phillip Handler) for Rockefeller Medicine. The entire scheme was designed to keep Rockefeller medicine in power. Few. Eric Weinstein wants to know why Epstein was in his math dept at MIT. This is why. Control the scientific narratives, control what gets funded and published, control what gets studied and what get buried to Pubsmear (Elisabeth Bik) and then you auction off Nobel Prizes and give them to researchers whose science leads to no cures.
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2.x.com/DissidentMedia…
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DID YOU READ THE NEW MKULTRA BLOG YET? patreon.com/posts/cpc-78-n…
3. Are you paying attention Savages? I doubt it.
A new, compact, high-power microwave weapon, the TPG1000Cs, has been developed at a Shanghai Nuclear Technology Institute, which could become one of the most serious threats to the Starlink satellite network.
The device can deliver 20 gigawatts of energy for up to a full minute, the South China Morning Post reported, cited by Portfolio.
The TPG1000Cs, the world’s first compact driver for high-power microwave weapons, has been created at the Northwest Institute of Nuclear Technology in Shanghai. The device can deliver 20 gigawatts of power for up to one minute.
At just four meters long and weighing just five tons, the device is small enough to be mounted on trucks, warships, airplanes, or even satellites. Some Chinese experts estimate that a ground-based microwave weapon with a power of over 1 gigawatt could be capable of seriously disrupting or even damaging satellites in low Earth orbit, such as Starlink, being used in the Russian-Ukrainian war.
Previously known similar systems could operate continuously for no more than three seconds and were much larger. The Russian Sinus-7 drive, for example, was operational for about a second, delivered about 100 pulses per shot, and weighed up to 10 tons.
China has repeatedly signaled that Starlink poses a serious threat to its national security. Chinese military researchers are currently developing new “Starlink killer” weapons, including high-powered microwave systems and lasers, that could be used to relatively cheaply combat large constellations of low-orbit satellites if necessary.
SpaceX has lowered the orbital altitude of its Starlink satellites to reduce the risk of collisions. But that makes them much more vulnerable to attacks from ground-based directed energy weapons. If China eventually deploys the TPG1000Cs in space, the invisible strikes could be even more devastating.
Erika Kirk family DEW Microwave weapon was used to harvest Maduro from Venezuela so the Zionist could cpature the oil and refine it in Citgo refinies in the USA that one of Miriam fiends just bought on the courthouse steps for 7 billion. YOU'RE SLEEPING.
This new blog is more explosive than the Epstein files, that I promise.
patreon.com/posts/150408576
Richard Helms, the Director of Central Intelligence, ordered the destruction of the vast majority of CIA MKULTRA documents in January 1973. He believed these were all the records. The original MKULTRA work was done at Tulane University in the Dept of Neurology and Neurosurgery in the 1950s and 1960s and he was unaware of this. Much of that work was linked to the Tulane Primate lab. Delgado's work in bulls was copied by the Tulane researchers.
The program, first began with drugs moved to wired technologies and then ended in wireless technology using polarized light from screens. Final patents for screen use to control the nervous system of humans were filed in 2003 by people known to be linked to US government contracting and DARPA. The drugs were given to primates and humans. The program involved administering Mexican Peyote and LSD and other drugs to unwitting human subjects, was highly controversial, illegal, and immoral. Helms ordered the destruction of the files during a period of intense scrutiny following the Watergate scandal and as he was leaving office.
Helms sought to erase the evidence of the planning and approval of these test programs to prevent public outrage and ensure no one would be prosecuted. He also knew about the rumors of forming the Church Comission which was being done to examine and audit the illegal activities in the CIA at this time. Frank Church was a Senator from Kentucky. As Helms was forced to resign by President Nixon in 1973, he ordered the purge as one of his final acts to protect the agency and his subordinates.
He left an executor behind to finish the job of document destruction. The Executor was Sidney Gottlieb. I spoke about him briefly with RFK Jr in the Rick Rubin Tetra podcast. The destruction of MKULTRA was authorized by Dr. Sidney Gottlieb. He was the head of MKULTRA, who ordered the files shredded. The chief of the CIA Records Center protested the destruction of these files on February 2, 1973, but the order was carried out anyway. Despite the 1973 order, a cache of approximately 20,000 documents survived because they were misfiled in financial records rather than subject files, which were discovered in 1977.
In 1989-1991, I found a cache of 16 boxes of MKULTRA data from the Tulane University Dept of Neurology and Neurosurgery. All the science in this blog was discovered in those boxes in the basement of Charity Hospital. Charity Hospital was flooded by by Hurricane Katrina in 2005. The NOPD and NO Fire Dept said that the basement areas were flooded all assets of the hospital were destroyed and cleared as salvage. I've referenced what I found in many podcasts but this blog contains the hardcore science data I found and I put together as a resident at LSU neurosurgery. The CIA sought to prevent congressional investigators from discovering the extent of the experiments, which involved over 80 institutions including universities and hospitals.
2. The collateral effects of the blog above for kids stuck in the Rockefeller paradigm of medicine?
Jaundice, Heteroplasmy, and Transgenerational Epigenetics: The Warning Flare that shows up in the NICU.
The baby's matirx becomes loaded with atoms it cannot use to clear the toxin. Bilirubin build up in the skin and brain alter the fluorescence of both organs and this changes how both organs work. Normally UV fluorescence is a function of cholesterol and melanin in the skin and brain.
Bilirubin can significantly interfere with the UV fluorescence and light absorption properties of the skin, though it doesn't do so by changing the melanin itself. Instead, bilirubin acts as a "competitive absorber" and a fluorophore in its own right. Here is how that interaction works:
1. Absorption Overlap
Melanin is a broad-spectrum absorber, meaning it soaks up light across almost the entire UV and visible spectrum. Bilirubin, however, has a very specific "peak" absorption around 450–460 nm (blue light).
When you shine UV or near-UV light on the skin:
Melanin absorbs the light to protect the lower layers.
Bilirubin absorbs the light in that specific blue-green range.
The Result: If you are looking for the specific "glow" (fluorescence) of melanin or other skin components, the presence of bilirubin acts like a yellow filter, "stealing" the light before it can reach the melanin or blocking the resulting fluorescence from reaching your eyes/sensors.
2. Bilirubin’s Own Fluorescence
Bilirubin is actually fluorescent under certain conditions. When exposed to specific wavelengths of light, it can emit its own glow.
In medical diagnostics, researchers use skin fluorescence spectroscopy to measure bilirubin.
If you were to look at the skin under a Wood's Lamp (UV blacklight), high levels of bilirubin can alter the expected reflection. While melanin usually looks dark/void under UV, bilirubin can introduce a "muddy" or sickly hue that masks the crispness of the melanin's appearance.
3. The Phototherapy Connection
This relationship is actually the basis for treating jaundice in infants. We use Phototherapy (blue light) because:
Bilirubin absorbs the light energy.
That energy triggers a chemical reaction (photoisomerization).
The bilirubin changes into a water-soluble form that the body can excrete.
The Melanin Factor: This is exactly why phototherapy is LESS efficient in babies with high melanin levels. The melanin "competes" for the light, absorbing it before it can reach the bilirubin in the blood vessels, often requiring a higher intensity of light for treatment. NICU's stopped using UV light in my training!!!!
^^^^This is why when I was in medical school I always asked why we went away from UV light to treat jaundiced kids and the answer I always got back was retinal hyperplasia damage. I pointed out that studies all had medotholgy problems, never considered skin pigment levels and were sponsered by Rockefeller medicine foundation. They advocated for blue even thought blue light would add more mass to the childs matrix and age it right in the hospital. It was infuriating.
Jaundice in a baby which is yellow skin from bilirubin buildup (5-20 mg/dL vs. normal <1) screams trouble, and it’s tied to my decentalized dance. It’s a neon sign of heteroplasmy that mtDNA mutations piling up in utero, skewing the Fe²⁺/Fe³⁺ atomic fulcrum. The baby is adding mass to its body for no reason at all. Then you add in all the metals from the jabs they get. No wonder they are not all cretins.
Pregnancy gone wrong (hypoxia, ROS spikes, maternal stress) loads fetal tissues with defective mtDNA (10⁻⁵/bp/division, 10x normal). Bilirubin, from heme breakdown (Fe²⁺ oxidized to Fe³⁺), floods when liver mitochondria falter and this affects cytochrome c oxidase (Cu, Fe) and Q-cycle stall (NADH/NAD+ ratio +50%, per neonatal studies). You should have seen the faces of the OB's when a neurosurgery resident call them idiots when I showed them how the Q cycle worked. They are dumb asses.
NO binds Fe²⁺ too long (g = 2.03 persists), O₂ starves (pO₂ < 20 mmHg), and biophotons dim (10⁴ photons/cm²/s, sluggish growth and horrible repair is inborn in the kid in the ICU and the centralized fucks do not know it. Parent have no idea what their light addiction just caused.
Transgenerational epigenetics seals it; maternal mtDNA lesions (8-oxo-dG up 3x, per oocyte sequencing) pass down, amplified by ROS (0.5 mM in utero). Paramagnetic sync with Earth’s field frays that Fe²⁺/NO can’t toggle, Co/Mn falter, VEGF lags (angiogenesis -30%). your babies germ line has a 30% higher heteroplasmy rate.
Jaundice flags this: a baby’s tissues, choked with heteroplasmy, can’t regenerate like Becker’s kids did with torn off finger tips because voltage drops (+2 mV early), biophotons fade (10³ photons/cm²/s), and Fe³⁺ dominates (g = 4.3). It’s epigenetics 101 and the pregnancy’s chaos scars the next generation’s electromagnetic web. Not bueno at all. Rockefeller medicine is like going to the Zorro Ranch with no cell phone.
3. Dynasties must fulfill their destinies. Paradigms are like dynasties. Paradigms, like Rockefeller medicine must enforce their dynasties. Nature is different because life is nature’s dynasty.
My decentralized thesis strikes the final chord of the Quantum Biological Manifesto. I
’ve identified that the "Manufactured Dynasty" of modern medicine is essentially a Thermodynamic Lie; a sprawling edifice of "obfuscations and equations" designed to ignore the singular, simple truth that Life is a Light-Mediated Time Crystal.
When the environment (the conditions of existence) is decoupled from the internal "Nockchain," the dynasty of Nature is overthrown by the chaos of entropy.
The "Truth" is simpler than any equation: We are beings of Light, governed by Time.
The "Dynasty of Nature" can only be restored when we stop trying to "push and pull" our biochemistry with mechanical interventions.
We must return to the Conditions of Existence that created us: The Morning Sun, the Cold, the Ground, and the Sunset "Fountain of Youth."
Decentrlaized medicine shifts the MDs perspective by moving medical practice from Rockefeller "Pharmacological Management" to "Environmental Engineering." It acknowledges that the clinician’s role is not to "fix" the patient with material inputs, but to restore the Quantum Coherence of the patient's internal matrix so the body can heal itself according to the laws of physics.
My curiosity has revealed the "Nockchain" of reality. The only question remains: Are we brave enough to delete the manufactured dynasty and live by the laws of the Sun?