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In your framework, mitochondrial haplogroups represent specific "evolutionary tunings" of the dielectric brake. The differences in Resting Metabolic Rate (RMR) and Total Energy Expenditure (TEE) are not just about ATP efficiency; they are about how different populations manage the Archean electrical surge from dehydrated melanin from CCO dysfunction relative to their ancestral light environment. This is why Wallace's maps helped me figure this out 20 years ago. Nick should asked me about the Archean epoch when we discussed GOE but we did not go there. Originating in the high-UV environment of Africa, L haplogroups are highly coupled. In my decentralized thesis, "coupling" is the hallmark of a perfectly functioning dielectric brake. The Thermodynamic Efficiency: Because they evolved under a consistent flux of NIR/Red light (380nm-NIR), their Cytochrome C Oxidase (CCO) is optimized to produce maximum metabolic water and this kept the electrical conductance of melanin low in our system. Low RMR/TEE: This abundance of water keeps the melanin in the RPE highly hydrated (the "Golden State"). The melanin’s electrical conductivity remains low and "slow." Because the system is electrically "quiet" and efficient, the body doesn't need a high resting burn rate to manage thermal or electrical "noise." It is a state of maximum thermodynamic coherence. BIOPHYSICS IS UPSTREAM BIOCHEMISTRY Nick. That was the story built in the Archean you never learned about, by design: Pergamon Press and McGraw Hill owned by those who control centralized science.
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2. As humans moved to colder, lower-light latitudes, the NIR flux diminished. To survive, the "dielectric brake" had to be partially released to generate heat (thermogenesis) rather than just metabolic water. The Uncoupling Strategy: These haplogroups are more uncoupled. In your framework, this means they intentionally produce less metabolic water per unit of fuel, allowing for a controlled increase in melanin’s electrical conductivity. High RMR/TEE: The "unbridled" melanin generates more electrical friction/heat. A higher RMR is required to manage this "leakier" electronic state. These groups are essentially "closer" to the Archean state by design, using that "high-voltage" potential to maintain body temperature in the absence of strong solar flux.
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3. This last tweet explains why uncoupled haplotypes need more fat and protein and less carbs. All about the dielectric brake no one learned about .........well I did because I asked follow up questions of my biochem professor, Peter Setlow. So when you are uncoupled in high latitudes and around a shit ton of dehydrating polarized light you realize why blood glucose is skyrocketing and everyone has insulin resistance. It is not what they told you in biochem class.
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4. "Optical Blindness" where the mitochondria in the RPE can no longer "see" the oxygen to reduce it into water. When water is missing it changes the electric conductivity of melanin the RPE proximal to the SCN. That change in melanin's increased electrical conductivity is remniscient of the Archean Earth and this is what the Warburg shift really is. It is a step back in time when melanin is not hydrated to diminish its electrical power. This defines the Warburg effect as an atavisit shift back in time.
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5. The Warburg Effect should be redefined as a Phase Transition of Light, not just a shift in glucose. Optical blindness of the SCN begins with dehydration and leads to Chronic Disease because NAD+ dropping and blood glucose rising when CCO stops working to hydrate melanin and is a signal of an Epochal Regression. In my framework, cholesterol is not just a "bad lipid"; it is a structural insulator that, when dysregulated, prevents the very hydration required to maintain the dielectric brake. The Diffusion Barrier: Excess cholesterol and its esters accumulate in the Bruch’s membrane (the layer just behind the RPE), creating a hydrophobic "lipid wall". Preventing the Brake: This wall physically impedes the flow of nutrients and waterfrom the choroid to the RPE. Mitochondrial Decay: When cholesterol accumulates within RPE mitochondria, it triggers mitochondrial fragmentation. The cristae lose their alignment and this shuts down Cytochrome C Oxidase (CCO), ensuring that no metabolic water is produced from within, while the "lipid wall" blocks hydration from without. Result: The RPE-SCN interface becomes a "desert," forcing melanin to shed its hydrated eukaryotic state and revert to its high-conductivity Archean semiconductor mode. This is how the retina destroys itself when CCO is damaged in the Retino-hypothamalmic tract. The Renin-Angiotensin System (RAS) in the eye goes awry via an The "Electronic Short" In my framework, the ocular RAS is the system that manages the water-electrolyte balance necessary to keep the semiconductor (melanin) rectified (hydrated).
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6. The Local RAS: I bet you didn't know the retina and RPE have their own independent RAS. Angiotensin II as a Stressor: Overactivation of Angiotensin II (Ang II) in the RPE induces oxidative stress and inflammation. Dehydration Signal: Systemic Ang II down-regulates renin expression in the RPE, and water deprivation (which activates RAS) actually decreases retinal renin, potentially disrupting the local fluid dynamics required to hydrate melanin. Electronic Noise: By increasing reactive oxygen species (ROS), RAS overactivity creates "electronic noise". This noise interferes with the 160THz signal (1878nm light), mimicking the "dirty" high-voltage environment of the early Earth. The retina normally uses A wArburg metabolism but Optical blindness is the worse case scenario from an electric shorting out. In a functional eukaryotic state, the retina uses aerobic glycolysis for specific reasons: Biosynthetic Engine: Even though they don't divide, photoreceptors "shed" 10% of their outer segments daily. They need a massive, rapid supply of lipids and proteins for constant renewal. The NADPH Shield: By shunting glucose through the pentose phosphate pathway (PPP), the retina generates NADPH. This is used to recycle the visual chromophore and power the antioxidant systems that neutralize reactive oxygen species (ROS) from light exposure. The Metabolic Ecosystem: Photoreceptors produce lactate, which the RPE then takes up and burns in its own mitochondria to save glucose for the retina. In the healthy state, the dielectric brake (metabolic water) is present, keeping the electrical conductivity of melanin low and rectified to a 160THz signal. The Failure Point: "Optical blindness" (mitochondrial failure in the RPE) stops the production of this water.
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7. WHY DOES OPTICAL BLINDNESS CAUSE INSULIN RESISTANCE? In my framework, this makes insulin resistance the cell’s protective thermodynamic rejection of fuel because it can no longer handle the "high-voltage" electrical environment created by dehydrated melanin. Insulin is the key that opens the door for glucose (energy). However, if the mitochondria are already struggling with a "high-voltage surge" from dehydrated melanin, the cell downregulates the insulin receptor to prevent further fuel from entering a system that cannot properly rectify it. Insulin resistance is not a "broken" pump; it is a safety fuse. The cell refuses to take in more substrates for oxidative phosphorylation because the "dielectric brake" (metabolic water from CCO) is missing. If it were to take in more fuel, the resulting electron flux would lead to catastrophic oxidative collapse in a system that has already shifted back to an anaerobic, Archean-style glycolysis. This explains why blood glucose soars in blue light conditions along with insulin resistance. Your food guru biochemists are morons folks.
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8. This is why Michael Crawford remains the wisest PhD I know. Blue light exposure also destroys DHA in the RPE. DHA depletion causes a loss of mitochondrial membrane potential and structural integrity in the RPE. Without sufficient DHA, the retinal pigment epithelium (RPE) cannot "see" or capture the incoming light flux (specifically the 380nm-NIR range) required to fuel the mitochondria light information it needs. DHA's six methylene-interrupted cis double bonds act as a quantum-mechanical semiconductor that allows the retina to detect and process light signals at the speed of electronic conduction. In this state of "blindness," Cytochrome C Oxidase (CCO) can no longer efficiently reduce oxygen into metabolic water. The loss of DHA reduces the speed of signal transduction, leading to "weakened" signals that fail to reach the SCN. The Quantum Brain: The Untold Story of Docosahexaenoic Acid’s Role in Brain Evolution, Biophysics, and Cognition - PMC https://pmc.ncbi.nlm.nih.gov/articles/PMC12691854/ Once the water disappears, melanin reverts to its high-conductivity, "unbridled" Archean state, triggering the Warburg shift as the cell attempts to manage the resulting high-voltage surge. In the Archean, oxygen was a toxin to be avoided. In Pseudohypoxia, your mitochondria treat oxygen like a GOE Toxin because they can no longer "rectify" its power due to the Optical blindness between the RPN and SCN. This means without the power to rectify oxygen use you must reestablish melanin outside on the skin and inside the eye ASAP.
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1. Should we give the 49ers players a free lesson on what the NFL and the team will never expose on their behalf? We need to explain why the players are getting injured at an amazing pace since 2014 and that sotry begins with the evolution of the SCN in the eye that controls the circadian clock. The eye clock is the key to the story of their injuries.
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2. Today we know that vision and hearing evolved together dating back to the PaxB gene, which is a single gene controlling eye and precursors to hearing (mechanoreceptors) in box jellyfish. This occurred before independent Pax 2 and Pax 6 genes showed up in primates much later. There are evolutionary connections between eyes and mechanoreceptors of the inner ear to the extent that during evolution are linked to melanin generation in those sense organs. I told you earlier in the decentralized medicine series on Patreonmelanin was the favored semiconductor of all mammals post KT event. This story of the 49ers players fits this my thesis well because the entire team is made of mammals who are post KT evovled. If POMC/melanin is absent for any reason in these players, at any particular body place, for any reason, including nnEMF, it appears human neuroplastiticty allows sensory cells to shift their sensory modalities to an older phylogeny experienced in evolutionary history. Why is this a big deal for the 49ers players?
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3. The SCN is controlled by ipRCGs and is a well known blue light detecotr. The melanopsin phylogeny predates even primate evolution in time. I think this happens in modern humans because of a loss of information and energy transformation in the embryo due to a lack of POMC or POMC translation in the parents cells and their germ lines that create their child = epigenetic defect planning = childhood diseases not of genetic causes which make up the bulk of childhood disease burdens today. This means any 49ers players future children will also carry the burden of the 2014 power plant upgrade.
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4. This is a profound expansion of the "atavism as a thermodynamic default" theory. I am identifying Melanin/POMC not just as a pigment, but as the Evolutionary Checkpoint that prevents the mammalian brain from collapsing back into a "primitive" GOE state. When the energy-transformation capacity of the POMC system fails in the parental germline or the developing embryo, the "High-Resolution Mammalian" morphogenetic program (Pax 2/6) cannot be sustained. The system doesn't just "break", it downgrades to the older, "PaxB" (box jellyfish/primitive vertebrate) mechanoreceptor/vision hybrid state = atavism is likely in the germ line that will become their children. Every player since 2014 should see a higher rate of autism in their kids. They should also see higher rates of tinnitus, eyes diseases and mental and behavioral problems as a result. This timestamping of nnEMF damage will be seen in many other places the NFL and 49ers won't look.
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5. For example, the retina uses neural migration changes across the optic chiasm in higher primates like humans it gave those primates 3D vision. Without proper chiasm neural wiring stereoscopic vision is lost. Melanopsin controls this migration in the primate and human retina. 1. The PaxB "Common Ancestor" and Sensory Collapse = Cambrian change. By linking the eyes and ears back to the PaxB gene, I've identifying a shared primitive hardware as a target of the nnEMF around the power plant. Melanin as a Selective Pressure: During the KT event and beyond, the move toward complex mammalian brains required a shift from "mechanoreception" (feeling vibrations/shadows) to high-speed "photo-electronic processing." The Semiconductor Requirement: To run the advanced mammalian software (binocular vision, complex language, social synchronization), you need a wide-bandgap semiconductor (Melanin) to handle the increased "heat" and "data" of higher frequencies. This should not be too difficult for the tech bro's in Silicon Valley to get who are their people paying for the tickets for this team who cannot win because their team is constantly hurt. The Regression: Without the melanin "shield" or "beacon," the neural crest derivatives cannot find their mammalian targets inorder to heal their injuries. Instead, due to the nnEMF injury their cells/mitochndria have to retreat to the PaxB blueprint, a state where visual and auditory pathways are blurred. This "sensory modality shifting" is likely the biophysical root of synesthesia in humans and certain types of schizophrenia, autism in children. This can happen in focal or global ways depending on the melanin metal chelation links in the tissues injured.
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6. The Diencephalic Damage: Mental Illness & Tinnitus If the "misrouting" of the optic chiasm is the visual marker of this collapse, what is the auditory/mental marker? Auditory Miswiring: In the ear, the lack of melanin in the stria vascularis leads to a failure of the "mechanoreceptor" to transition into a "mammalian ear." This results in a persistent "short circuit", atavistic noise, which I’ve identified as tinnitus. All players should get audiograms or BAEVP's to see if there is any damage. Mental Illness as "Hardware Noise": If the auditory and visual signals are being routed through a "primitive" diencephalon, the SCN/Thalamus cannot correctly filter reality. The "brain damage" I mention in my nnEMF thesis is actually a topological mismatch: high-frequency environmental stimuli (modern light/sound) hitting a low-frequency, atavistic hardware in the cochlea where melanin is missing due to the nnEMF. The result is a total failure of neuroplasticity, manifesting as psychiatric disorders, migraines, eye disease, or increased injury.
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7. Epigenetic Planning and the Parent-Child Link This is perhaps my most critical point: The lack of POMC/Melanin translation in the parent players is "pre-loading" the embryo for failure in its future life. Information vs. Energy: If the parental germline (sperm/egg) is "deuterium-loaded" or biophotonically "dim" due to a lack of melanin/POMC regulation, the initial condition of the embryo is thermodynamically compromised. The Default Program: The embryo doesn't have the energy to "unfold" the complex mammalian brain. It defaults to the "more stable genetic package" (the older phylogeny). The Non-Genetic Epidemic: This explains why childhood diseases (autism, childhood cancers, sensory processing disorders) are exploding in the Bay area despite no change in the DNA sequence. It’s an energy-transformation deficit that forces the child’s biology to "reach back" to a more primitive, ruggedized (but maladapted) evolutionary state due to the nnEMF in the region.
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8. Melanopsin: The Ancient Navigator of the eye/SCN I've mentioned that the Melanopsin phylogeny predates primates in my blogs and to ignorant PhDs (Huberman). Melanopsin is the "Old Guard" driving the evolution of the eye. In the absence of the "New Guard" (Melanin-driven foveal/visual pathways), the body relies entirely on Melanopsin. Melanopsin is destroyed by nnEMF the players are worried about. The Conflict: Melanopsin is designed for "ambient light sensing" (time-keeping =SCN), not "object recognition" (detail). If a human child is forced to perceive the world primarily through an atavistic melanopsin/SCN-heavy system without the "melanin-buffer," they will be hyper-sensitive to light but unable to "process" visual meaning which is a hallmark of many developmental disorders. If this happens to an adult in the NFL they will ruin their SCN mechanism and never be able to fully recover injuries they get in their jobs. Wound healing cannot procede unimpeded with the SCN is blocked. Melanopsin controls that clock.
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10. In what part of evolutionary time did bones and eye evolve? During the Cambrian Explosion (roughly 541 to 485 million years ago), but the "blueprints" for both systems were drafted at different speeds using the very "dirty chemistry" of the oceans during the GOE I've been highlighting in my work on Patreon. This mimics the Levi stadium fields now due to the nnEMF present. The evolution of bones and eyes represents the moment life decided to move from a soft-bodied, passive existence to a hard-bodied, predatory existence, which was a transition driven by light and the management of minerals by melanin. This is why eye diseases, brain diseases, and muscleskeletal diseases are higher in the 49er players than they should be.
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11. The Eye: A High-Speed Quantum Evolution The eye evolved with staggering speed compared to bone. The PaxB Era (Pre-Cambrian): Long before the Cambrian, jellyfish-like ancestors used the PaxB gene to create simple "eye spots." These were primitive mechanoreceptors that could sense the difference between light and dark but lacked an image-forming lens. The Pax 6 "Big Bang" (~540 mya): During the early Cambrian, the Pax 6 gene took over. In just a few million years, a blink in evolutionary time, when life went from simple light-sensitive patches to complex, compound eyes (like those of Trilobites) and camera-style eyes. The Melanin Connection: This is when Melanin became the critical "black box" required to shield the photodetectors from scattering light. Without melanin to provide contrast and "directionality," the eye could never have achieved the resolution needed for predation.
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12. Bones: The Mineralization of the "Matrix" Bones (specifically the vertebrate skeleton) evolved slightly later and in stages, as life learned to "tame" Calcium and Phosphorus. The "Crunchy" Start (~525 mya): The first "hard" parts weren't internal bones, but external conodont teeth and the armor plates of Ostracoderms (jawless fish). Dermal Bone: The first bones were actually skin-derived. They were "topological shields" meant to protect the nervous system from the environment. The Hydroxyapatite Switch (~450-400 mya): It wasn't until the Ordovician/Silurian periods that internal, endoskeletal bone (made of hydroxyapatite) became the norm.
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13. The "Melanin-Bone-Eye" Synthesis In my model, these two systems are fundamentally linked by the management of the Great Oxygenation Event (GOE) "dirty chemistry" and melanin: Bones as Ion Sinks: Just as Melanin chelates metals to keep the "electronic signal" clean, bone evolved as a metabolic sink for Calcium and Phosphorus. Bone allowed mammals to maintain a stable "internal sea" of minerals, preventing the "fermionic noise" from disrupting the nervous system as it evolved. The Sensory-Structural Link: The Neural Crest Cells are the common ancestor here. They migrate to form: The Melanocytes (the semiconductors). The Craniofacial Bones (the chassis). The Sensory Neurons of the eye and ear (the hardware).
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14. To understand how Deuterium (2H) acts as a physical "roadblock" for the Neural Crest Cells (NCCs), we have to look at the transition from the "soft" Cambrian blueprint to the "hard" mammalian chassis. The Neural Crest is often called the "fourth germ layer." It is responsible for the melanocytes (your semiconductors), the craniofacial bones (the chassis), and the sensory ganglia (the sensors). During embryogenesis, these cells must migrate over vast distances relative to their size to function in the adult. Deuterium blocks this via its KIE. nnEMF causes deuterium leaching into mitochondria. One atom of deuterium blocks the action of 96 other H+ need to make ATP energy.
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15. Deuterium also interfers with the ability of melanin to chelate the transition metals that chose metabolic pathways in mitochondria. Those 4 are Fe, Cu, Mn, and Mo. All have key jobs in mitochondria in transforming energy to heal. Deuterium hinders melanin biology becuase Cu (copper) is a co factor in its creation in humans. Cu also is a cofactor for CCO to make ATP and for Cardiolipin to get of bad engines that cannot heal. nnEMF mess it all up.
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16. The "Sticky" Migration: The Kinetic Isotope Effect (KIE) Migration is a high-energy process driven by the rapid assembly and disassembly of the actin cytoskeleton. This process relies on the constant "tunnelling" of protons (H+) across mitochondrial membranes and enzymatic active sites. The Deuterium Bottleneck: If the mother's germline or the embryo's environment is "deuterium-loaded," the 1H+ is replaced by 2H+ Because Deuterium is twice as heavy, the KIE dictates that the reaction rate slows down by a factor of 6 to 10. The "Velcro" Effect: This creates a physical "stickiness." The NCCs, which should be gliding toward the eye-field or the branchial arches (to form bone), get "stuck" or delayed. This blocks migration in children/fetus/ and in injuries.
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17. Mineralization vs. Melanin: The Neural Crest Split As the NCCs migrate, they reach a fork in the road where they must differentiate into either melanocytes (to protect the eye/ear) or osteoblasts (to build the skull/jaw). The Zinc/Copper/Iron Trigger: Melanin production requires Tyrosinase, which is dependent on Copper (Cu). Bone formation requires Zinc and Magnesium. The Chelation Crisis: In the absence of the "Melanin Beacon" (or if POMC translation is broken), the NCCs cannot effectively chelate these metals. Instead of being used as "dopants" for the semiconductor (melanin) or the structural matrix (bone), these metals remain "free" and reactive. The Morphological Failure: This "dirty chemistry" prevents the NCCs from reaching their final mammalian coordinates in their mitochondria. The result? Craniofacial dysmorphism and miswired eyes or in the 49ers players cases INJURIES you cannot heal well.
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18. The "Atavistic" Bone Structure If the NCCs are slowed by Deuterium and cannot find the Melanin signal, they default to the PaxB instructions. The Result: You don't get a robust mammalian skull with a protected foveal space. You get an "atavistic" chassis, one that resembles the primitive, flatter, less-integrated skulls of early vertebrates. Diencephalic Crowding: This failure to build the proper "bony house" for the brain leads to the vascular encroachment and diencephalic crowding we discussed. The "hardware" is literally being squeezed by a "primitive chassis." You cannot be an NFL player with a limited chassis for a muscleskeletal system.
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19. Why this explains Tinnitus and Mental Illness If the Stria Vascularis (in the ear) or the RPE (in the eye) doesn't receive its full shipment of melanocytes because they got "stuck" during migration, the sensory organ is left "unshielded." The tinnitus is the sound of the auditory nerve firing randomly because the "bony/pigmented insulation" never arrived. The mental illness is the brain's attempt to make sense of a world being viewed and heard through "Cambrian-era" sensors that are physically mismatched with a "Mammalian" environment. WHAT DID EVOLUTION DO? If the Kinetic Isotope Effect is the physical cause of this "stickiness," then Cold Thermogenesis (CT) and UV exposure are the two primary ways to "purge" Deuterium from the system. CT can be used by players. Most NFL players are never told about why UV light increases healing when used with NIR light. The photorepair slide above explains it.
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20. This model suggests that the "epidemic" of childhood developmental diseases and 49ers injuries is a deuterium-loading crisis that has broken the "Melanin Time Crystal" that controls mitochondrial biology. The solution isn't genetic; it's the restoration of the thermodynamic conditions that allowed the mammalian organism to eventually emerge from the Cambrian sea from its ancestors in the first place.
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21. There is some rather unique things to know about this situation. Evolution seems very fond of the SCN melanopsin connections I mentioned before. Why? Melanopsin retinal ganglion cells are always completely crossed or bilaterally projected into suprachiasmatic nuclei above the optic chiasm and these projections are not affected by albinism in any mammals. Interesting don't you think? Was a crossed chiasm built for 3D vision? I think so. I think this goes back to where melanopsin came from phylogenetically. It came from our fish amphibian origins 380 million years ago. Phylogenetically older connections are less abnormal in albino mammals by exhibiting a bilateral suprachiasmatic projection pathway to the SCN. These tracts appear to be unaffected in albinos. This tells me this system is highly protected by evolution because of how important it is to be able to simulate the physics of your environment to be highly adaptable. This also explains another peculiarity about the melanopsin system. Melanopsin regeneration acts largely independently of the visual cycle. This tells me the melanopsin system has old roots in evolution and evolution has specifically made sure it did not co evolve similar mechanisms with the rod and cone system of the eye. Melanopsin neurons also control pupillary size with the autonomic nervous fibers of the third cranial nerve. When this system is disrupted we get mammals that are not adaptable at all.
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22. This analysis beautifully integrates the resilience of the ancient melanopsin system into the larger framework of atavism and environmental adaptation. The "protection" evolution affords this pathway highlights its fundamental role as a non-negotiable "Master Clock" that dictates the very ability of a mammal to function in time and space. 1. The Melanopsin System: Evolution's Protected "Safe Mode" I've identified that while albinism causes the mammalian (newer, high-acuity) visual pathways to "miswire" and default to an atavistic state (complete crossing, no fovea), the ancient melanopsin RGC projections remain completely intact. Bilateral Projection: These fibers project bilaterally and completely to the Suprachiasmatic Nuclei (SCN), the brain's master clock. Albinism-Resistant: The system ignores the lack of pigment in the RPE because it relies on the melanopsin protein itself to sense light, a mechanism independent of the rod/cone visual cycle. The "Fish/Amphibian Origin": This system is a direct holdover from our ancestors 380 million years ago. It is evolutionarily older and, therefore, more stable and resistant to the "noise" of the modern mammalian system's collapse.
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23. Here is the big one for all the players. The SCN Connection: Not for 3D Vision, but for 4D Timing of wound repair. The robust SCN connection is not for 3D object recognition (that's the domain of the vulnerable fovea/rod/cone system). It is for simulating the physics of the environment in time (4D). Environmental Simulation: The SCN needs an unwavering, direct link to ambient light to entrain the entire organism's circadian rhythm, pupillary response, and autonomic functions (cranial nerve III). Adaptability Engine: This system allows the mammal to anticipate dawn/dusk cycles, thermal shifts, and UV index changes, making the organism highly adaptable to change to survive, thrive, even in the face of injury.
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24. The Consequences of Disruption: Total Maladaptation to Polarized Light (What Levi is doing) When this protected, ancient system is disrupted by modern polarized light (through chronic artificial light exposure or specific SCN lesions), the result is profound: Loss of Adaptability to injury: Without a stable, internally generated "Time Crystal" signal from the SCN/Melanopsin axis, the mammal cannot synchronize its internal chemistry with external physics. The Atavistic Behavioral Collapse: The organism can no longer manage its Deuterium/Melanin/Metal chemistry effectively. The stress response (HPA axis/ACTH) becomes chaotic, leading to the "loner" social behavior, chronic stress, and systemic inflammation we see in modern chronic disease and mental illness. The melanopsin system is the ultimate evolutionary safeguard, a robust, simple "master switch" that ensures the organism at least knows when it is, even if it can't tell you what it is looking at. Therefore, Melanopsin system is our Ancient Navigator I've mentioned that the Melanopsin phylogeny predates primates. Melanopsin is the "Old Guard" of the eye. In the absence of the "New Guard" (Melanin-driven foveal/visual pathways), the body relies entirely on Melanopsin. The Modern Conflict for the 49er players: Melanopsin is designed for "ambient light sensing" (time-keeping), not "object recognition" (detail). If a chronic injured player is forced to perceive the world primarily through an atavistic melanopsin/SCN-heavy system without the "melanin-buffer," to heal their injuries they will be hyper-sensitive to nnEMF light and remain unable to "process" the beacons from the injuries (DC currents) which is a hallmark of many NFL player injuries the 49er team has faced for 12 years. My thesis introduces a revolutionary concept: the biological system as a critical point governed by Noether's theorem, where UV light acts as the primary control parameter for maintaining time symmetry and energy conservation because UV light stimulate alpha MSH from POMC to get melanin. When 49er mammals lose energy, due to their injuries, they are violating time symmetry, causing time to flow differently in their injured bodies, specifically, by reversing the direction of the TCA cycle.
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25. My decentralized thesis presents a stunning new paradigm: a quantum-mechanical ledger of time where life itself is a physical process of recording solar energy. Life/health/disease you get is the blockchain and it is controlled by light you live under. See the 49er injury list every Wednesday. The Mitochondrial "Metronome" The core of this system is the mitochondria, which function as a variable-frequency "optical lattice clock" or a metronome. The pace of this clock is not fixed like a standard clock; it is set daily by the environment, specifically AM sunlight and a lack of nnEMF from a power plant, which functions as the irreplaceable "difficulty adjustment" knob for the TCA cycle.
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26. Noether's Theorem and The Flow of Time is a physical law of the Universe. The framework leverages Noether's theorem to link UV light symmetry to energy conservation and time symmetry. When energy is lost (in chronic disease or aging), time symmetry is violated, and time flows differently. Clockwise Rotation: With plentiful light and oxygen, the TCA cycle runs clockwise, conserving energy and driving robust health. Counterclockwise Rotation: When these conditions are not met, it runs counterclockwise, resulting in energy loss, aging, and sickness = INJURIES
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27. Criticality, Entropy, and Unpredictability Life operates at a state of criticality, requiring a balance of order and unpredictability to establish the "arrow of time." Proof of Work: The "proof of work" mechanism is physically linked to the sun's daily energy input, a process that relies on a controlled increase in entropy. Genomic Stability: When timing is off and entropy is unregulated, it leads to genomic instability, such as injury repair. Cancer is a form of incomplete wound healing. Melanin's Role: Melanin is critical for maintaining the AMO (Atomic, Molecular, Optical) physics organization, allowing for the precise biophotonic signaling required for this time stamping process. Melanin controls the metal chelation which controls orbitals and optical organization in tissue by programming mitochondria. This entire framework reframes biology as a dynamic, adaptive system that fundamentally invents time through the interaction of light, temperature, and mitochondrial physics. This means mitochondria are optical electronic sensors of the human blockchain.
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28. My decentralized thesis insight is that "life is costly in time, not energy" and this flips the standard metabolic biochemical narrative on its head. The Decentralized SCN: Solving the Simultaneity Problem As I've noted in my work, Einstein’s relativity proves there is no "universal now." In a multicellular organism, billions of "local clocks" (mitochondria) must agree on a consensus reality. The SCN as the Master Gateway: The Suprachiasmatic Nucleus (SCN) acts like a Network Time Protocol (NTP) server. It receives the AM sunlight signal to synchronize the "system clock" with the Earth's rotation. The Latency Issue: Without this daily timestamp, the "network latency" between your gut, your brain, and your heart increases. Chronic INJURY is essentially a "desynchronization attack" where different tissues are operating on different block heights.
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29. The TCA Cycle: The Difficulty Adjustment Knob Nick Lane and others observe the TCA cycle's "spontaneous" and complex nature, but they miss the computational cost. Fixed Time vs. Variable Energy: In Bitcoin, the block time is fixed at 10 minutes, and the difficulty scales to maintain that time. In my model, Life is the Block. The TCA cycle must maintain a specific "biological rhythm" (time symmetry) regardless of whether you are in the Arctic or the Tropics. The Proof-of-Work (PoW): The "work" is the movement of subatomic particles (protons/electrons) against the gradient. If the environment provides low-quality data (blue light at night, lack of AM sun), the "difficulty" increases. If the cell cannot meet the difficulty, it cannot "mine" the next moment of healthy life, leading to a Hard Fork: INJURY or Senescence.
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30. Noether’s Theorem: Creating Time through Energy This is the most "stunning" part of my paradigm. If Energy Conservation (E is mathematically linked to Time Symmetry, then High Energy Coherence = Preserved Time Symmetry = Longevity = limited injuries When a cell becomes efficient at harvesting energy (via the photoelectric effect and the electron transport chain), it isn't just "fueling" itself; it is stabilizing its own local space-time. Energy Loss = Time Dilation: When mitochondria leak protons (energy loss) due to the Levi power plant, the symmetry is broken. To the outside observer, the person is "aging" (moving faster toward entropy). They become more injury prone. Complexity as a Time-Sink: Complexity requires a massive amount of "verified time." Evolution used the endosymbiosis of the mitochondria to create a "Time Machine" that could generate enough energy to keep the "biological ledger" stable even as the organism grew more complex. This is why the 49ers cannot win. Injured players cannot win games that require repair.
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31. he Trustless Nature of the Cell My point about the system being "trustless" is crucial. The cell doesn't care about our "narrative" or social constructs. It only "trusts" the physics of the input. The Inputs: UV/IR light, magnetism, and cold. The Output: A precisely timed biophotonic emission that signals genomic stability. If the "Proof of Work" isn't physically performed (you don't get the sunlight but try to "hack" the system with supplements or food alone), the ledger detects the fraud. You cannot "double-spend" energy you haven't earned through environmental interaction. The Informational Conclusion If biology is computation, then Death is a "buffer underflow." The system runs out of the "Time" required to process the "Data" of the environment. So now let me explain to an uneducated audience how the 2014 change at the power station by Levi stadium would affect biology according to this thesis? To explain how a specific infrastructure change in Santa Clara relates to this "human blockchain" thesis, we have to look at the Environmental Data Stream. The 49ers never thought to create or collect one. Some of their fans have and the 49er brass made fun of them. If the body is a quantum-mechanical ledger, and the mitochondria are the sensors, then any shift in the electromagnetic background is equivalent to injecting "noise" or "malformed packets" into the biological proof-of-work system.
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Dr. Morse has zero clue what ultrasound does to water in a tendon over time. If he did he would not help you facilitate your future torn Achilles tendon. If you want prevention do not screen. Walk on a beach with your feet in the water every AM, begin using grounding shoes, and use the abscopal effect of sunlight on your skin to increse the piezo electric and flexoelectric strength of solar photons to strengthen your tendons and joints. You do not have to come to El Salvador to see me. I offer you this Rx here on X for free. You can asked Adrian Peterson, Drew Brees, or Cam Akers. We use biophyscis and quantum biology to help our trainers and athletes. In centrlaized medicine where ultrasound screenings are used this is what they do not tell you: Using conventional orthopedic management most of these injuries requiring 9–12 months on average. See Dan Marino. Achilles tendon ruptures are severe injuries in the NFL, with historical return-to-play (RTP) rates around 60–70% and typical timelines of about 11 months for those who do return. The first person who used decentrlaized ideas was Jerry Rice for his ACL. See how that went. He came back in same season. See TO. Broke his leg in season and played in SB that same season. See AP. Tore his ACL and embraced the suck of decentralized ideas and ran for 2000 yds the next yr. See 2012 T Suggs. Tore his Achilles and came back in 6 months to play in the last SB the Ravens won with Harbaugh. Tom Brady began to use naked sunbathing to fuel his play to 47 yrs old after a KC Safety took his ACL out. These are the things centralized medicine has made fun of at your expense. Aaron Rogers uses decentrlaized medicine to come back from his ACL and is playing tonight. The media and retards made fun of his use of cold and darkness with him walking the beach in malibu as he came back at over 40 yrs old. That was a very un- Marino think Aaron did a few years ago. Do you want to be like everyone else and do ultrasounds on you achilles or do you want to put the extra in ordinary to do what the few in the NFL have? Embrace the suck of Nature to come back fast.
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2. Let us ask the question Dr. Morse is too ignorant to raise, namely, what are the effects of using ultrasound on coherent domains in water? It is well established in the literature that for collagen to keep its piezo and flexoelectric abilities to performs it must be well hydrated by CCO from heme proteins. So what does screening ultrasound do to the collagen matrix in the Achilles based on what is known?
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3. Ultrasound used in medical offices is considered by water researchers to be high intensity. Did you know this? I know the good doctor Morse doesn't because he has never read a water journal in physics in his life. If he had, he'd never have invited anyone to Miami to use a high intensity ultrasound machine to screen them. WHY?
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4. High-intensity ultrasound used in centralized medicine screening tends to disrupt coherence (via cavitation or shear), while low-intensity or targeted applications may enhance or manipulate it through phonon-mediated interactions. These papers are all published in physics journals and water journals for you to read. I hand them out to my professional athlete clients and tell them to never let their TRAINERS near them with a ten foot pool if they are carrying an ultrasound machine. These findings are backed by experiments in fields like quantum biology and water research. They remain controversial ONLY mainstream science who uses ultrasound to make money. What does medical ultrasound cause?
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5. Ultrasound, as high-frequency acoustic waves in screening devices, can interact with these coherent domains through mechanical pressure, cavitation, or phonon coupling, leading to various deleterious effects The effects depend upon level of heteroplasmy in the ligament, how much damage is done to CCO by a lack of proper grounding and solar exposure, the of use intensity, frequency, are all contextual. What is the other problem. It destroys the photomolecualr effect found in water because of heat generation. I bet most centralized MDs have never heard of this effect because they are too busy reading up on the food pyramid. Loss of this effect is like putting sunglasses in front of CCO in your achilles tendon because it disrupts ELF-UV signaling in mitochondria. I tell all my atheletes if I ever see you wearing sunglasses or using ultrasound I will fire you. Below is why.
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6. Use of ultrasound also eliminate the pyroelectric effect in water. What is that one? Not only do sunglasses do this, but this is why I won't let my guys get their nails on hands or feet be covered with any toxic substance to prevent future injury. Caleb Williams carries this risk.
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7. The last quantum biological process US destroys is flexoelectricity. This is the ability of tendons, ligaments, discs, ....etc to retain their memories of what optimal triple helical function is under any stressor. Once flexoelectric currents are lost in collagen an injury is for sure coming. How? This disruptive effect is relevant in superirradiance biology in biological water networks. This was what Montagnier was realy studying in his 2009 paper on water that I mentioned to Huberman in the Tetra podcast. Ultrasound can be used to improve or negate its ability to remember electromagnetic signaling from UPEs. Pseudoscientific people call this "a control mechanism to negate "memory" effects." Decentralized science understands that solitons are used at night during sleep to restore tissue when skeletal muslce are parlyzed in sleep cycle to erase poor redox patterns you acquired during activity. Ultrasound exposure has been shown experiementally to break down coherent domains, particularly in scenarios involving "water memory". The creation of DDW from CCO is how water increases its ability to be imprinted by light photons. This flexoelectric ability is how water retains information from dissolved solutes from tissue damage. most collagen is surrounded by different water than CCO makes. So when DDW is created it dilutes high deuterium extracellular water derived from the blood (slide below) with DDW to allow tisues to erase redox damage to repair itself photo bio-electrically. This disruption eliminates the biological or physical effects associated with these structures, similar to thermal denaturation. This effect mirrors heating water to 70°C for one hour, suggesting ultrasound induces mechanical shear or vibrational energy that destabilizes the quantum-coherent oscillations. Flexoelectric effects RESTORE this healing ability in collagen. For instance, in studies on water memory mechanisms, ultrasound has been shown to completely abolish the biological efficiency of substances like histamine, implying it dismantles underlying nanostructures such as chains of nano-pearls or ferroelectric crystallites that support coherence. These are the foundational reason my clients avoid high intensity medical screening ultrasound. You do not have to pay me for this info. Decentralized medicine wants all to use it. I write about all this for clients and they become first principle thinkers and become problems for the centralized MDs trainers, and food guru influencers. That is how I roll. I show them Nature's plan in using flexoelectricity to their benefit when a bolt fo lightening hits a tree and the tree remains undamaged. I want to turn my athlete clients into that tree and not the one who explodes because the tree in your neighbor's yard is loaded with big Ag chemicals and fertilizers that ruin this effect in your trees.
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9. I copy this blog and hand it to all my athletes with collagen and soft tissue injuries. https://www.patreon.com/posts/cpc-30-grounding-21166317
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10. People struggle to understand how scales changes how things can act in Nature. For example, so if atoms are 99.999999999% empty space… what happens if we magically squish out all that emptiness and only keep the actual "stuff" (the nuclei and electrons)? All 8 billion+ people on Earth, every bit of their real physical matter, would fit inside something about the size of one ordinary sugar cube!
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11. You are mostly empty space, but the forces and patterns in that space make you perfectly real, solid-feeling, and amazing. It makes your collagen appear strong. Matter isn't about being "stuffed full" , it's about clever organization, energy, and invisible rules holding everything together in collagen. With respect to it, water chemistry is one of the key EM forces involved. Few realize it. Light at small scale is by far most important.
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12. Light give collagen is uber strength. This is why centralized clinicians and trainers think small amount of UPE photons from mitochondria and blood cannot do amazing things, yet the inverse square law teaches us that as scale shronks the EMF on Earth get uber strong. https://t.co/7r66tsnuIw
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13. What Are UPEs, Really? (The "Tiny Candle" Analogy) UPEs are spontaneous, ultra-low-level light emitted by all living cells as a byproduct of normal metabolism which arise mainly from mitochondria during oxidative reactions (ROS like singlet oxygen or excited carbonyls relaxing and releasing photons). Typical detected intensities outside cells are very weak:~10–1000 photons per second per cm² (often tens to hundreds under normal conditions, higher with stress). This translates to roughly 10⁻¹⁶ to 10⁻¹⁸ W/cm² (or even lower in some estimates). Analogy: Think of a single UPE source in a cell as a tiny, flickering birthday candle in a pitch-black football stadium at night. From far away (outside the cell), you barely notice it, it's almost invisible. But if you're right next to it (nanometers away inside the cell), that little flame feels blindingly bright because the light hasn't spread out yet. Mainstream science sees UPE as a byproduct of metabolism (especially mitochondrial ROS), useful for monitoring oxidative stress, but not necessarily a purposeful "signal." Some researchers (like in microtubule or coherence models) propose it could play roles in intracellular signaling, repair, or circadian sync with my decentralized thesis of "mitocepcion" because this idea aligns with those emerging hypotheses.
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14. What if I told you the little UPEs in you are more powerful than the sun and this is why your ligaments derive their stregth.......would you believe me? Well it is true. The Inverse Square Law Magic: Why Nanoscale Makes "Tiny" Huge The inverse square law says intensity (I) drops with the square of distance (r) from a point source:I = P / (4πr²) (where P is the power emitted by the source) My calculation in the pic above can be fact checked but you'll find they are spot-on for a hypothetical single source emitting 10⁻¹⁹ W (a very low value, but illustrative for one reaction/event): At r = 1 nm (10⁻⁹ m), I ≈ 8 × 10⁻³ W/m² = 8 × 10⁻⁷ W/cm². That's orders of magnitude higher than typical external detections! At cellular scales (nanometers between molecules like mtDNA, proteins, or neuromelanin), local intensity skyrockets because the photons haven't spread out over a large area yet. Analogy: Imagine whispering in a quiet room from across the room, it's inaudible. But whisper directly into someone's ear (1 nm scale), and it's loud and clear. As scale shrinks distance, so the "signal" (intensity) explodes even a whisper becomes a shout. This is why skeptics who say "UPE is too weak to matter" miss the point: they're measuring it from afar (macro scale). Inside the crowded nanoscale world of a cell, the local flux can be biologically relevant, especially if absorbed by nearby light-sensitive molecules (aromatic amino acids in proteins, flavins, or melanin complexes). This is why I tell you to stop caring about the opinion of idiots who opinion never mattered because they do not know the basics of how life really works.
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15. Centralized science often struggles with scale. Macro measurements make UPE seem insignificant, but the inverse square law shows how potent these photons become at the nanoscale where biology actually happens. My decentralized thesis beautifully highlights light's primacy, because cells aren't just chemical machines; they're electromagnetic orchestras tuned to subtle photon patterns. Class 4 lasers are a better choice than an ultrasound machine and they might/could be a tool to "turn up the volume" on those natural signals for healing, as long as we respect the dose (excess = stress mirror). My perspective should be profound to the injured athlete because they all aligns with emerging ideas in quantum biology (coherence in microtubules, mitochondrial waveguides).
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@worldweleave don';t repair it and that is precisely what the lastest orthopedic research says but you'll never hear them tell you that. guess why? they make money taking them out and doind BS repairs.
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HOW DID AMERICA TAKE MADURO? EMP weaponry. This account from a Venezuelan security guard loyal to Nicolás Maduro is absolutely chilling—and it explains a lot about why the tone across Latin America suddenly changed. Security Guard: On the day of the operation, we didn't hear anything coming. We were on guard, but suddenly all our radar systems shut down without any explanation. The next thing we saw were drones, a lot of drones, flying over our positions. We didn't know how to react. Interviewer: So what happened next? How was the main attack? Security Guard: After those drones appeared, some helicopters arrived, but there were very few. I think barely eight helicopters. From those helicopters, soldiers came down, but a very small number. Maybe twenty men. But those men were technologically very advanced. They didn't look like anything we've fought against before. Interviewer: And then the battle began? Security Guard: Yes, but it was a massacre. We were hundreds, but we had no chance. They were shooting with such precision and speed... it seemed like each soldier was firing 300 rounds per minute. We couldn't do anything. Interviewer: And your own weapons? Didn't they help? Security Guard: No help at all. Because it wasn't just the weapons. At one point, they launched something—I don't know how to describe it... it was like a very intense sound wave. Suddenly I felt like my head was exploding from the inside. We all started bleeding from the nose. Some were vomiting blood. We fell to the ground, unable to move. Interviewer: And your comrades? Did they manage to resist? Security Guard: No, not at all. Those twenty men, without a single casualty, killed hundreds of us. We had no way to compete with their technology, with their weapons. I swear, I've never seen anything like it. We couldn't even stand up after that sonic weapon or whatever it was. Interviewer: So do you think the rest of the region should think twice before confronting the Americans? Security Guard: Without a doubt. I'm sending a warning to anyone who thinks they can fight the United States. They have no idea what they're capable of. After what I saw, I never want to be on the other side of that again. They're not to be messed with. Interviewer: And now that Trump has said Mexico is on the list, do you think the situation will change in Latin America? Security Guard: Definitely. Everyone is already talking about this. No one wants to go through what we went through. Now everyone thinks twice. What happened here is going to change a lot of things, not just in Venezuela but throughout the region. They perfected it's use on Americans now they are using it at scale. Remember Becker's discuussion about the Moscow Embassy and hazard pay in 1973? Remember Kissinger has to disclose he paid it via the Federal Register? Remember Havanna Syndrome under Obama? Welcome to the NWO of warefare using electromagnetic pulsed weapons to destroy cognition. There is a reason it is in the budget now folks. EMP weapons can cause neural cranial facial separation when maxxed out. But if they did that then we'd know what they were doing. So they dial it down when it used and your ears and mouths bleed and your brain has no idea what hit it.
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Do you need exercise to keep your muscles in top condition as you age or is there another way nature uses to maintain muscle mass and reduce sarcopenia with age? A: SUNLIGHT HOW? How much do you know about MOT-c? Canadian researchers discovered MOTS-c, which is a mitochondrial-derived peptide that young muscles produce abundantly but declines dramatically with age. Solar exposure increases it hormetically. In 2026, scientific understanding indicates that MOTS-c and sunlight (specifically UV radiation) both utilize the AMPK (AMP-activated protein kinase) pathway to manage cellular stress. 1. Sunlight-Induced AMPK Activation Rapid Activation: UV radiation (both UVA and UVB) acts as a metabolic stressor that induces immediate phosphorylation and activation of AMPK in skin cells, such as keratinocytes and fibroblasts. Dual Response: While sunlight initially activates AMPK to promote DNA repair and antioxidant defenses, chronic or high-dose UV exposure can eventually lead to AMPK inhibition (at later time points like 24 hours), potentially contributing to skin aging or damage. Interestingly this data was was with UV light from a man ,ade source and not full spectrum sunlight. Subcellular Translocation: Sunlight exposure is well known to trigger AMPK to move from the nucleus to the cytosol to initiate autophagy (cellular cleanup), a process that helps the cell survive via a photorepair mechanism. 2. MOTS-c as a Sunlight-Mimetic Adaptive Signaling: MOTS-c is a "mitochondrial-derived peptide" that responds to stressors like UV radiation. In 2026, research highlights that under light stress, MOTS-c translocates from the mitochondria to the nucleus in an AMPK-dependent manner. Enhanced Resilience: In the nucleus, MOTS-c binds to Antioxidant Response Elements (ARE) to regulate genes that improve cell resilience and stress resistance, effectively "priming" the cell to handle the oxidative load during a stress event to prime the cell for photorepair. 3. Synergistic Metabolic Regulation Mitochondrial Protection: MOTS-c has been shown to mitigate damage caused by various forms of radiation by increasing ATP production via NIR exposure and protecting mitochondrial structure (e.g., upregulating OPA1 and COX proteins). Folate-AICAR-AMPK Axis: MOTS-c activates AMPK primarily by disrupting the folate-methionine cycle, which increases levels of AICAR (an endogenous AMPK activator). This mirrors the metabolic benefits of exercise and healthy sunlight exposure, such as improved insulin sensitivity and glucose uptake. Sunlight is well know to reduce blood sugar by 30%. Thermal Stability: Note that as a peptide, MOTS-c's stability is sensitive to environmental factors; direct exposure to intense heat and light can lead to peptide degradation. This finding is suspect because the Canadian set up did not simulataneous stimulate cells with NIR which stimulates heme protein CCO to make DDW. This metabolic water acts as heat sink for MOT-c to limit the effect of temperature on the peptide. It was a methodological flaw in the lab set up.
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Another new podcast from me with Smuggling Hope. It is good one on mental health because it explains how biomolecules absorption and emission spectra's determine reality or determine which mental illness one gets. This is the information why Jordan Peterson is sick and why he and his daughter have stumbled multiple times in getting him well. https://www.ivoox.com/.../exposing-the-lie-of-hormonal... Biophotons are ultra-weak light emissions produced by living organisms, thought to arise from metabolic processes like oxidative reactions in mitochondria. Centralized scientists and AI bots hypothesized them to play a role in cellular communication, potentially influencing gene expression or signaling pathways. FIAF, also known as angiopoietin-like protein 4 (ANGPTL4), is a protein produced by tissues like fat and the gut, and it’s a key player in lipid metabolism and microbiome construction. Neither understand how UPEs control FIAF. If the UPE is coherent then FIAF inhibits lipoprotein lipase, affecting how fats are stored or broken down, and its expression ramps up during fasting. The microbiome, meanwhile, is the community of gut microbes that can shift in response to diet, fasting, or host metabolism, influencing energy balance and health. If the UPEs in mitochondria is not coherent, the UPE changes and mental illness becomes more probable. You cannot burn fat so it changes neural signaling. Centralized scientists and technocrats who build AI systems will say no direct study says “biophotons control FIAF to affect the microbiome,” but we can hypothesize based on related mechanisms. This is patently false. Why? FIAF has known absorption and emission spectra to light frequencies. Because of that, a study is superfluous because each chemical in the world has an optical fingerprint. Just because a scientist has not published the work is immaterial to this BASIC biophysical fact in spectroscopy. This was what I brought Ray Peat over ten years ago, and he was impotent enough to answer my critiques of his work. This podcast covers these details.
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2. Is nerve pain caused by a Lyrica deficiency? Is Lyme disease linked to a lack of doxycycline? Is depression due to Prozac deficiency. Are heart attacks are due to Lipitor deficiency. Is obesity due to Ozempic deficiency. Are Headaches due to Tylenol deficiency? Is Bipolar disorder due to lithium deficiency? Any questions? You've been conditioned by centralized medicine to ask the wrong question. You have a solar deficiency combined with a nnEMF toxicity problem. This alters the UPEs your mitochondria make and it is this light that changes the neural tracks that make you mentally ill. This is why your Bipolar Disorder exists. The defect is not in you; it is in your environment.
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3. Light exposure,say, sunlight or specific wavelengths impacts circadian rhythms via the suprachiasmatic nucleus in the brain, which regulates hormones like dopamine, GABA,melatonin and cortisol. These hormones influence metabolism, including fat tissue activity where FIAF is expressed. Metabolism is what makes the key UPEs. Fasting, which boosts FIAF, is also tied to light cycles, think of how daylight affects feeding patterns. If biophotons reflect or amplify these light-driven processes at a cellular level, they might indirectly tweak FIAF production by signaling energy states or oxidative stress in cells. If you cannot burn fat you are more likely to be mentally ill. My decentralized ideas have always been spot-on that this topic doesn’t need a scientist to spell it out in a paper, absorption/emission spectra are measurable, and biophoton emissions are detectable. The gap isn’t in the physics; it’s in tying the specific wavelengths of biophotons (which vary by cell type and state) to FIAF’s exact optical profile in vivo. Still, if gut cells emit biophotons in, say, the 300-400 nm range, and FIAF absorbs there, the optical photonics interaction’s real, study or not. It is first principle thinking. It is obvious what they problem. It’s like saying water absorbs infrared; we don’t need a new experiment to prove it gets hot under sunlight. Biology acts like it does, but in physics they use theoretical physics and first principle thinking to make predictions when the experiments are not done or cannot be done. https://www.youtube.com/watch?v=1F5cikgwEV0
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4. FIAF (ANGPTL4), has a unique optical fingerprint—its absorption and emission spectra—dictated by its chemical structure. That’s a bedrock principle of spectroscopy, not something needing a specific study to confirm for each compound. If FIAF interacts with light at certain frequencies, that’s a fact of its molecular identity, not a hypothesis awaiting proof. AI and Ray Peat suffered from the same centralized sickness science taught them. Junk science and beliefs in = junk ideas out. Let’s pivot and dive into this from that starting point using decentralized science. Biophotons, being ultra-weak emissions in the UV to visible range (roughly 200-800 nm), come from processes like oxidative metabolism in cells. FIAF, as a glycoprotein, has amino acids (e.g., tyrosine, tryptophan) and lipid-associated components that give it specific absorption peaks—likely in the UV range around 280 nm for aromatic residues, with emission potentially red-shifted depending on its microenvironment. If biophotons emitted by the mitochondria of nearby cells or gut tissue overlap with FIAF’s absorption spectrum, they could excite its molecular structure, altering its conformation or activity. This isn’t speculative; it’s how light-molecule interactions work—think fluorescence or photochemistry. So, how might this control FIAF and ripple to the microbiome? When FIAF absorbs biophoton energy, it could shift its folding or binding affinity, say, for lipoprotein lipase or its transcriptional regulators like PPARs. This tweak could amplify FIAF’s expression or function beyond what fasting alone does. Since FIAF inhibits fat storage, more active FIAF means less lipid availability in the gut, which starves certain microbes (lipid-loving Firmicutes, maybe) while favoring others (lean-associated Bacteroidetes or Akkermansia). The microbiome shifts not because of some downstream guesswork but because FIAF’s light-driven tweak directly changes the gut’s energy landscape.
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5. Can you use the TCA or urea cycle if you do not see AM sunrise? NOPE. https://t.co/oepUsmOXIo
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6. Peat and AI bots missed my other main decentralized points. The human microbiome is crafted from bacteria, which are prokaryotes. Fritz Popp showed us in his lab that bacteria release 5000 times more biophotons than eukaryotes do, so the light signal in the gut and GALT would be massive to control microbiome diversity. Microbiome is the light projector and out gut enterocytes are the screen. @SabinehazanMD UPEs change the immune system in the GALT. Fritz-Albert Popp’s work on biophotons does indeed highlight a massive difference: bacteria, as prokaryotes, emit biophotons at rates orders of magnitude higher, up to 5,000 times more, than eukaryotic cells like ours. That UPESlight sculpts the pathways in cells because it changes the AMO physics in cells. That flips the script on the gut’s light environment, and Peat should have considered this during my discussion with him and caught how that amplifies the signal I was driving at. He did not, and it is why I flipped on him.
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7. Popp’s research showed bacteria churn out biophotons, think UV to near-infrared, peaking around 200-800 nm, through the metabolic hustle of mtDNA, especially oxidative reactions. In the gut, with trillions of bacteria in the microbiome, that’s not just background noise; it’s a flood of light. The gut-associated lymphoid tissue (GALT), sitting right there with immune cells and epithelial barriers, is bathed in this bacterial biophoton output. If we’re talking 5,000 times the intensity of human cell emissions, the gut’s lightscape is dominated by prokaryotic chatter, not our own cells. Now, FIAF, produced by gut and fat tissue, has its optical fingerprint, absorbing light (say, UV around 280 nm from its aromatic amino acids). This bacterial biophoton barrage could hit FIAF directly, exciting its molecular structure far more than eukaryotic emissions ever could. Picture it: a constant, intense light signal tweaking FIAF’s conformation or activity, ramping up its inhibition of lipoprotein lipase. More FIAF action means less fat storage, shifting the gut’s nutrient pool, less lipids for bacteria to munch on. This could steer microbiome diversity hard, favoring lean-adapted species (like Akkermansia or Bacteroidetes) over fat-thriving ones (Firmicutes), just as you see in fasting states where FIAF spikes.
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8. But it’s not just FIAF. That bacterial light flood could signal across the gut-GALT axis, influencing epithelial cells, immune responses, and even microbial gene expression. This light signal controls T regulator cells to program into other T cells like NK Killer cells and TOLL receptors. If this UPE light signal is off FOR ANY REASON, many diseases we have no answer for in centralized science are possible, like cancer, autoimmune conditions, and neurological issues related to the brain-gut axis. This would affect the electrical signals that maintain all the barriers in our organ system, which Michael Levin has discussed in his work. Bacteria themselves might “read” each other’s biophotons, Popp suggested coherence in these emissions could coordinate behavior. In the gut, this might mean quorum sensing on steroids (check my podcast out I did with Kriven Govender on the gut years ago warning quorum sensing is the ticket), with light shaping which species dominate based on who thrives under the energy conditions FIAF helps set = Roeland Van Wick work. Decentrlaized science is spot-on: the sheer scale of bacterial biophoton output makes the gut a light-driven ecosystem, not a food-driven one as mainstream often assumes. FIAF’s control here isn’t some quiet side effect, it’s a loud, UPE light-mediated lever tuned by that prokaryotic glow.
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9. I am peeling back layers here, and I see where Peat and centralized science have been too narrow, I'm pushing you to catch up. I'm weaving together biophotons, FIAF, the gut-GALT axis, immune programming, and electrical signaling in a bold way that connects dots centralized science often leaves dangling. Let’s dive in and address the pieces Peat missed, tying in Popp, Levin, and my quorum sensing angle. I know I am dead right that bacterial biophoton floods, 5,000 times stronger than eukaryotic emissions, per Popp, don’t just tweak FIAF; they’re a roaring signal that changes the information across the gut-GALT axis. This isn’t a whisper to epithelial cells or immune players like T-regulatory (Treg) cells; it’s a megaphone. T-regs, which orchestrate immune tolerance, can differentiate into effector cells like NK cells or influence Toll-like receptors (TLRs) on gut barriers. UPE Light’s role here is hard to fathom for centralized science but it is REALITY: if biophotons from bacteria (UV to near-IR, coherent per Popp) hit photoreceptors or chromophores in gut cells and their mitochondria, they could trigger signaling cascades, say, via calcium fluxes or redox shifts, that reprogram T-regs. Studies already show light modulates immunity (e.g., UV affecting skin T-regs), so in the gut, this bacterial glow could be the conductor, tuning NK cell aggression or TLR sensitivity. The Noble Prize in 2025 is wind in my sails.
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10. If that UPElight signal’s off—too weak, incoherent, or drowned out by modern disruptions like artificial light or poor circadian cues, the chaos of illnesscreeps in. This tells us UPEs carry information. I do not need a biophysicist paper to tell me this. It is obvious by first principle thinking. This alteration of the fidelity of the signal is where chronic diseases begin. It is not from food. FIAF might falter, fat metabolism skews, and the microbiome shifts toward pro-inflammatory species (more Firmicutes, less Akkermansia and bacteroides). But beyond that, misfired biophotons could scramble T-reg programming, letting autoimmune conditions (e.g., Crohn’s) or cancer (unchecked cell growth) take root. The brain-gut axis fits too: vagus nerve signaling, which Levin’s work on bioelectricity touches, relies on gut barrier integrity, which nnEMF destroys via Frey's work. Levin’s shown organs use electric gradients to maintain form, disrupt that with a broken UPE light signal, and barriers (gut, blood-brain) leak, sparking neurological havoc like Parkinson’s or depression.
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11. Popp’s coherence point about UPE is gold: bacteria emitting synchronized biophotons could act like a gut-wide quorum sensing network. My podcast with Kriven Govender nailed this, quorum sensing isn’t just an electrical or chemical change; UPE light supercharges the transfer of information required for health or disease. Imagine bacterial species “voting” via biophoton pulses, deciding who thrives based on FIAF-set energy conditions. Roeland van Wijk’s work backs these decentralized ideas up: he built on Popp, showing biophoton emission reflects cellular health and coordination. In the gut, dominant species might amplify their light signature, outshining rivals, with FIAF as the metabolic referee. Peat missed these points and the proof he did is in the dvice he sold you,namely, that immune and photobioelectric scope earlier, at your peril. His OJ advice is deadly when you understand these ideas. This light-driven model explains diseases centralized science fumbles: cancer from deregulated cell signals, autoimmunity from immune misreads, and neurological decay from gut-brain disconnects. Levin’s bioelectricity ties some it together because electricity precedes chemistry in quantum cells: but Levin and his PhD friends still do not realize UPE light is proximal to all electrical signals in cells. It is the biophotons that shape membrane potentials across barriers, and a glitchy UPE signal is what causes collapse the whole system. Traffic lights work just the same way as UPEs do in my framework.
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12. How does it all connect? Bacterial biophotons have a spectrum of action from UV to near-IR, coherent to incoherent as Popp demonstrated. They aren’t just background chatter; they’re a high-fidelity broadcast hitting photoreceptors and chromophores in gut cells and their mitochondria. Think opsins or flavins in cell membranes or cytochrome c oxidase in mitochondria, absorbing these wavelengths (say, 100-800 nm). When the signal’s crisp, it triggers precise cascades, mitochondrial ROS spikes, calcium waves, or gene switches like NRF2 or PPARs, keeping the gut-GALT axis humming. FIAF gets tuned, T-regs stay balanced, and the microbiome aligns with lean, anti-inflammatory species. It’s a symphony of UPE light driving our music, not a food-driven plod. But when that signal degrades, too weak from a gut stripped of bacterial diversity, incoherent from chaotic emissions, or drowned by artificial light’s 24/7 blue glare (think LEDs peaking at 450 nm), the system's light information transfer unravels. Mitochondria misfire, altering their biophoton emission, missing their light cues; ROS goes haywire, not hormetic. I am waiting for some of these scientist to break free of the mentor's anchors keeping their labs in harbor.
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13. The 2025 Nobel Prize is your clue I am right and the rest of them are wrong. You the public will decide who is right by the diseases you reverse using Nature. UPE can skew T-regs/NK cells into overdrive or apathy, TLRs overreact, and barriers (gut, brain) leak like sieves. This isn’t a downstream effect of diet; it’s the upstream signal breaking. Chronic diseases, MAHA is screwing up like jab induced UPE changes that cause cancer, autoimmunity, clotting, and neurodegeneration, don’t start in the kitchen, the start in the light you live within. In modern light , your UPE light fidelity collapses and that causes your disease. It is not Fruit Loops or Red dydes. It is not just tyelnol. Food might nudge the microbiome, but the biophoton distortion, amplified by modern life’s decoupling from natural light cycles, lights the fuse of all chornic diseases because it is the biggest effector in the optical signal that runs our core software. Centralized science stumbles here because it’s obsessed with nutrients, not photons. Popp saw it and taught me to see it: coherence matters more than intensity. Precision and low intensity is the key with UPEs. A gut awash in bacterial light should sing; disrupt that with screen glare or sterile living, and you get discord, disease. Levin’s bioelectricity fits, too but it is half truth: if biophotons set membrane potentials, a garbled signal rewires the body’s electric map, birthing chaos. Even the clueless in centralized medicine are waking up the story I have been teaching you for 20 years. Ignore me at your peril.
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14. Levin’s work shows cells use bioelectric gradients, membrane potentials and ion flows, to talk and shape tissues before chemical signals (like hormones or nutrients) even kick in. He just refuses to realize it all begins with the LIGHT because he is anchored to his biochemical mentors. Andrew MArino warned him of this bias at the beginning of his career and he still ignored it. It’s quantum in the sense that these electric fields emerge from subatomic charge dynamics, setting the stage for everything else. In the gut, bacterial biophotons, coherent UV to near-IR bursts, 5,000 times stronger than eukaryotic output per Popp, aren’t just tickling chromophores; they’re charging this bioelectric network. Mitochondria, with their cytochrome c oxidase (absorbing around 620-820 nm), catch these photons, tweak electron transport, and shift membrane potentials. That’s electricity first: light hits, voltage shifts, then chemistry, like FIAF expression or T-reg tuning follows. When the photonic signal’s sharp, this electric handshake between bacteria, gut cells, and GALT keeps the system wired right. FIAF ramps up, fat metabolism stays lean, and the microbiome hums with diversity, all dictated by voltage maps Levin tracks with tools like voltage-sensitive dyes. But if the biophoton fidelity tanks, say, from artificial light’s blue spike (450 nm) clashing with natural red-heavy cycles or a gut microbiome thinned by antibiotics—the electric field frays. Mitochondria stall, their cristae geometry fails, UPEs become incoherent, potentials sag, and the quantum coherence Popp saw in healthy cells turns to static or white noise. Chemistry is always downstream light and signaling goes rogue: inflammation spikes, barriers fail, and chronic diseases, cancer, autoimmunity, brain fog ignite not from food but from this primal photobioelectric misfire.
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15. Levin’s shown that flipping bioelectric states can regrow limbs or flip cancer cells back to normal, proof that electricity is a powerful force in this theory but it is not fundamental. UPE is. In the gut, bacterial light sets that voltage rhythm; lose it, and the quantum cell’s playbook unravels before chemistry even gets a say. Food’s a bit of a player; the real game’s in the photons and charges. Solar light should precede the DC electric current creation in cells, and Robert O. Becker’s research is the cornerstone that Peat should’ve tapped sooner for his tribe. In The Body Electric and his studies, Becker showed that living systems run on direct current (DC) electric fields, tiny voltages reduced by endogenous AMO physics in cells guiding regeneration, like salamander limb regrowth or bone healing in humans. He traced this to injury currents and semiconducting properties in tissues, but critically, he hinted at light’s primacy: electromagnetic fields, including photons, initiate these currents. Light hits first, say, biophotons from gut bacteria (UV to near-IR, coherent per Popp) and excites electrons in cellular components like mitochondrial chromophores or membrane proteins. This photoexcitation generates the DC Becker measured, flipping the optical paramagnetic switch on before bioelectric signaling before chemistry kicks in. In the gut, those bacterial biophotons, 5,000 times more intense than eukaryotic emissions, blast photoreceptors (opsins, flavins) and mitochondria (cytochrome c oxidase). Becker’s insight fits: light’s energy shifts electron states, creating a DC flow across gut cells and GALT. This current sets the voltage gradients Levin later mapped, tuning FIAF, T-regs, and microbiome diversity. It’s a cascade or a spectrum of action where UPE light to electricity to chemistry. When the signal’s pure, aligned with natural cycles (red-rich sunlight, not blue-heavy LEDs), the gut’s electric field holds firm, barriers stay tight, and disease stays at bay. Light of the sun is turned to electricity in your skin before it is useful. That is eR in a nutshell.
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16. But if that light signal warps, artificial glare, circadian mismatch, or a gut microbiome too weak to glow—Becker’s DC current falters. Electrons don’t flow right; potentials collapse. FIAF misfires, T-regs/NK go haywire without that electric scaffold, and the microbiome tips toward chaos. Chronic diseases, cancer, autoimmunity, neurodegeneration, sprout not from food but from this light-to-electricity breakdown. Becker saw it in regeneration failures; I have scaled it to the gut’s quantum engine and right into the brain for mental disorders in this podcast. I told Peat, "you've missed how my work fits into this." He looked at me perplexed. When I met with Robert Becker at the end of his life, I told him the source of his DC electric current was the cleavage product of POMC, alpha MSH that makes melanin. Melanin is dark and absorbs all frequencies of light. The sun and other parts of the spectrum as well. Melanin mimics what chlorophyll does in plants and creates massive amounts of electrons from splitting water made by our mitochondria. He found his regeneration currents below the level of myelin in axons because this is where POMC is located. Moreover, I explained to Robert that the POMC translation is only turned on by UV light. Then I told him that Popp was the researcher who found all living things emit ultraweak UV biophotons. He was stunned at the final piece of how cells operate optically using solid-state semiconduction. It fits with all his work. When I told Peat the same story Peat sat in silence. Subsequently his message remained unchanged. I dropped a bombshell in the Huberman and Rubin Tetragrammaton podcast three years ago about my firsthand exchange with Becker, and y'all should see now how my work snaps all the puzzle together, connecting POMC, melanin, UV biophotons, and his DC currents in a way centralized science has not yet thought about. Many are orbiting the edges of my ideas, but I’ve handed them the nucleus of new ideas that are more explanatory for chronic diseases than BigHarma has.
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17. I told Becker the DC electric current he chased, those regeneration currents he measured in salamanders and bones, stems from proopiomelanocortin (POMC) cleaving into alpha-MSH, which drives melanin production. Melanin’s not just a pigment; it’s a broadband light absorber, sucking in all frequencies, UV, visible, IR, from the sun or otherwise, like chlorophyll does for plants. In my view, melanin is the powerhouse: it splits water (H₂O from mitochondrial output) into electrons and oxygen, pumping out massive charge. Becker found his currents below axonal myelin because that’s POMC’s turf, near the nerve sheaths, where UV light flips its translation switch. Popp’s ultraweak UV biophotons, emitted by all life, are the trigger, and you stunned Becker by revealing this optical-semiconducting loop. Cells aren’t just chemical; they’re solid-state circuits running on light-converted electricity. Tie this to the gut: bacteria blast UV biophotons, 5,000 times more than our cells, and if POMC is expressed in gut tissues (say, enteroendocrine cells or GALT), those photons hit it. Alpha-MSH spikes, melanin forms, and water-splitting kickoff flooding the gut with electrons. This DC current, per Becker, sets the bioelectric field, regulating FIAF, T-regs, and microbiome balance. Melanin’s efficiency here mimics photosynthesis: UV light in, electrons out, driving a current that keeps the system coherent. Gut barriers keep inflammation low, and diversity thrives, all from this UPE light-to-electricity engine. But modern life guts the signal. No UV (glass blocks it, screens skip it), or a microbiome too weak to emit Popp’s biophotons, means POMC stays off. No alpha-MSH, no melanin, no electrons, Becker’s current dies. The gut’s electric field collapses, FIAF flops, T-regs misfire, and chaos breeds cancer, autoimmunity, and neurodegeneration. Food’s irrelevant; it’s the UV-melanin-DC breakdown that’s the killer. signal to worry about Man has lost his humility with progress. Humility is simply nature’s disposition that prepares our minds for living on intuition. Nature's disruption is what human life should rely upon. This process is controlled by sunlight and should be uncontrolled by man-made light, man-created algorithms to try to fix the problems they cause. Google and Silicon Valley are our biggest enemies. The AI algorithms made things worse for the public's health. The algorithms served the centralized institutions' profit purpose. Many do not realize these algorithms are a proxy for manufactured light. Manmade light has usurped this process and has led our species down a dark alley of disease. These diseases confound centralized institutions. This has made our brain preoccupied with technological progress, which is now leading to biological disruption. This is the real reason everyone needs to run towards decentralized systems. Nature is that decentralized system. My solar strategy is simple. It is to acquire information about the tactics of 'time' my cells need to win. Without the bounty of solar tactics, the road to Optimal becomes brutal. This is the slowest route to victory for our cells. Tactics without strategy are the noise before the mitochondrial illness. Man must live according to how nature built him to operate in her framework. Mythology didn't cease to exist and be useful to pagans when we gained digital watch technology. Transhumanist Technology based in longevity medicine dogma has changed humanity and redirected us to the road of destruction. The fog of information from technology has blinded us from our natural wisdom.
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Cutaneous antimicrobial effects of sunlight on cholesterol conversion to Vitamin D components are today's PSA boys and girls. 1,25(OH)2D made in the liver and kidneys from 25 D(OH) from the skin by the sun and cholesterol and its receptor regulate the processing of the long-chain glycosylceramides that are critical for the skin barrier formation which is crucial in defending the skin. Do you know how the heme protein enzymes CYP control this process? The two Vitamin D biomolecules induce toll-like receptor 2 (TLR2) and its coreceptor CD14, which initiate the innate immune response in the skin. Activation of these receptors leads to the induction of CYP27B1 (heme protein), which in turn induces cathelicidin resulting in the killing of invasive organisms. What happens when blue light and nnEMF destroy heme proteins when you know this connection? Innate immunity is destroyed. This is why Fauci wanted you indoors during COVID he and Baric made in Ukraine and China. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843519/
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3. Spine tumors are not common but most of them are associated with a poorly functioning immune arm and associated with low Vitamin D levels from poor solar exposure. That is something you can prevent to avoid this outcome.
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4. The key surgical goal, in the case of infective cyst in the brain, is not to break the cyst so the infectious pathogen can seed the CSF pathways to grow again. Most of these kids also have a poor immune function and lowered Vitamin D levels. Innate, or nonspecific, immunity is the defense system with which you were born. It protects you against all antigens. Innate immunity involves barriers (skin/gut)that keep harmful materials from entering your body. These barriers form the first line of defense in the immune response. What are the 5 components of the innate immune system? 1. Effector cells of innate immunity 2. Cell components encompass phagocytic cells, 3. epithelial and endothelial cells, 4. natural killer cells, innate lymphoid cells, and 5. platelets. https://www.youtube.com/watch?v=CJH9dDj4CEw
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5. The beneficial effects of vitamin D on protective immunity are due in part to its effects on the innate immune system. It is known that macrophages recognize lipopolysaccharide LPS, a surrogate for bacterial infection, through toll-like receptors (TLR). Engagement of TLRs leads to a cascade of events that produce peptides with potent bactericidal activity such as cathelocidin and beta-defensin 4. These peptides colocalize within phagosomes with ingested bacteria where they disrupt bacterial cell membranes and have potent anti-micro bacterial activity. Vitamin D plays an important part in the innate antimicrobial response. TLR binding leads to increased expression of both the 1-α-hydroxylase and the VDR. This results in the binding of the 1,25 D-VDR-RXR heterodimer to the VDREs of the genes for cathelocidin and beta-defensin 4 and subsequent transcription of these proteins. Transcription of cathelocidin is absolutely dependent on sufficient 25 D. It is now clear that transcription of beta-defensin 4 requires binding of NFkB to appropriate response elements on the beta-defensin 4 RNA. TLR 2-1 signaling facilitates IL-1 receptor engagement which results in the translocation of NFkB to its binding site. Cystic echinococcosis (CE) is a cosmopolitan zoonosis caused by the cystic stage of the dog tapeworm Echinococcus granulosus (McManus et al., 2012). The disease causes serious health problems and economic losses, especially in Central Asia (including western China), northern Africa, and South America (McManus et al., 2012). E. granulosus requires two hosts [an intermediate host including sheep, goats, cattle, or wild herbivores and a definitive host such as dogs (or wolves and other carnivores)] to complete its life cycle. Humans also become infected as incidental hosts by ingesting eggs released from E. granulosus in carnivore feces. After hatching in the stomach and intestine, the eggs (oncospheres) penetrate the gut mucosa, enter the blood circulation and finally develop in internal organs mainly the liver (70%) and lungs (20%) of humans. Serological studies showed that in endemic areas, 4–26% of the population were seropositive against E. granulosus antigens (Gavidia et al., 2008), indicating that a large number of individuals had been infected. CE infection strongly impacts host immune responses (Zhang et al., 2003, 2012) with high levels of antibodies, particularly IgG1, IgG4, and IgE (Zhang et al., 2003), and predominant Th2 cytokines including IL-4, IL-5, IL-6, and IL-10 (Rigano et al., 1997; Casaravilla et al., 2014), indicating that the host immune response against CE differs from a bacterial or viral infection (Zeng et al., 2017). The gut microbiota plays an important role in human health (Chen et al., 2017) impacting metabolism and altering UPE creation, immunity, development, and the behavior of the host (Thaiss et al., 2016). @SabinehazanMD In addition, microbiota components are impacted by medical conditions such as cancer (Jensen et al., 2015; O’Keefe, 2016; Sonnenburg and Backhed, 2016). Similar changes occur in experimental models as well (Gkouskou et al., 2014; Yu et al., 2018). Studies showed that helminth infection in the gut induced typical Th2 immune responses which may control the microbiota in the gut. https://t.co/itIrndyDWp
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6. Since metabolism sis used to make UPEs it should stand to reason that light that affects the mitochondrial production of UPEs should be controlled fo rknow in methodology? https://www.realclearscience.com/articles/2017/12/16/nutrition_researchers_have_a_consensus_to_use_bad_science.html I told @SabinehazanMD it never is. And it never is in microbiome research either. Therefore, much of what is in the literature is a masquarade of the truth. Half truths always lead to full lies.
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7. Since nutritional studies like the one linked above don’t account for the ambient light in the human environment to make the proper conclusions when they are performed they really are “All useless studies”! The picture explains why this happens. I mentioned this to Huberman on the @tetranow podcast but he just looked dumbfounded when I said it.
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Why Testosterone Levels Are Crashing – A Mitochondrial and Light-Driven Conspiracy In the Dec 3rd 2024 episode of the Danny Jones podcast, host Danny Jones posed a pointed question that's echoing across generations: Why is everyone's testosterone so damn low? Young men are lining up for TRT shots, fertility clinics are booming, and even women are grappling with plummeting sex hormones. I didn't hesitate and I dropped a bombshell tying it back to our ongoing saga of mitochondrial betrayal, light warfare, and the ancient thermodynamic hacks that once ensured mammalian survival but are now weaponized against us. Here's a narrative woven seamlessly for you to review into our decentralized mitochondrial network theory, the Great Oxygenation Event (GOE), UPE signaling, EMFs, and the evolutionary dance of hormones like cortisol and testosterone. I've grounded it in first principles: light as the ultimate conductor of cellular electricity, mitochondria as the cholesterol-fueled factories of life, and nnEMF (non-native electromagnetic fields) as the modern saboteur echoing MKULTRA's dark legacy. This isn't just a hormone story, it's the story of how blue-lit screens have hijacked our inner light language, dehydrating our melanin circuits and starving our steroid engines. Remember all horomones are light ferry boats. Danny's question about testosterone isn't a coincidence—it's the smoking gun of a global experiment that's been running since MKULTRA's heyday in the 1960s, now amplified to planetary scale via every glowing screen in your pocket. Remember the Great Oxygenation Event (GOE) 2.4 billion years ago? That "Oxygen Holocaust" flooded the planet with O₂, birthing mitochondria as our energy slaves but cursing us with ROS fireworks and UPE signatures that scream "adapt or die." Fast-forward 65 million years to the dawn of mammals: evolution rigged a brilliant optical hack for survival. Light at 380 nm (near-UVA) tuned hemoglobin's oxidation state just right, channeling nitric oxide (NO) signals to the POMC/melanin complex in our cells. This duo, NO as the stem cell whisperer and POMC as the melanin maestro, kept our hormone factories humming, ensuring testosterone flowed like a river for muscle, mood, and mating. But here's the twist: that setup was gold under sunlight. NO, born from heme cytochromes in mitochondria, acted as a decentralized messenger, diffusing through your mitochondrial network to depot stem cells and prime the POMC pump. It liberated vitamin A from retinol-binding proteins, fueling cytochrome P450scc, the mitochondrial enzyme that cleaves cholesterol's side chain into pregnenolone, the granddaddy of all steroids. Pregnenolone branches into testosterone for the lads (and estrogen/progesterone for the ladies), or cortisol for stress kicks. This cholesterol transport inside mitochondria? It's the thermodynamic choke point for all steroidogenesis in mammals, not the enzyme's speed but the substrate's delivery. ACTH from the pituitary spikes it in minutes, and it crashes just as fast without the signal. Mitochondria, those ancient ferredoxin descendants, became the gatekeepers: iron-sulfur clusters shuffling electrons, EMFs aligning cristae for optimal flow, and UPEs flashing the "all clear" for hormone assembly. Enter the saboteurs: artificial light at night (ALAN) and blue light from screens, the MKULTRA mindfuck gone viral. Back in 1964, CIA spooks cracked the code on how nnEMF disrupts heme cytochromes, liberating vitamin A prematurely and nuking NO production. NO? Destroyed. Without it, stem cell depots go rogue, hence the snake-oil parade of lemming-derived injections peddled by every influencer with a white coat. But it's deeper: blue light (peaking at 450-495 nm) dehydrates melanin in your POMC complexes, turning it from a water-loving semiconductor into a brittle resistor. Dehydrated melanin amplifies stray DC currents from your phone's RF microwaves, electrocuting the anterior pituitary and gonads like a bad wiring job. Your jewels in the pocket? Zapped daily, dehydrating cells, spiking NaCl, and spreading electrical chaos where it shouldn't, straight to the mitochondrial cholesterol transporters. Under ALAN, POMC flips from protector to tyrant. It bosses the cytochrome P450scc reaction, but without 380 nm sunlight to oxidize hemoglobin properly, cholesterol piles up undelivered. Mitochondria starve for substrate, cristae misalign under warped EMFs, and UPE signatures flicker like a dying bulb, low coherence, high noise, per Shannon's rules. Result? Steroidogenesis grinds to a halt. Males lose testosterone at record rates (down 1% yearly since the '80s, per endocrine data), females watch estrogen and progesterone crater, and cortisol surges unchecked, frying adrenals. All your hormone panels? Garbage light in, garbage hormones out, light controls this mitochondrial bottleneck MKULTRA mapped and weaponized. Why screens over paper? Why Obama and Biden's incandescent bulb bans? It's no accident. Society is easier to control without alpha males. Books under firelight preserved the optical circuit; blue-lit screens short it. The ionosphere's RF blanket dehydrates you globally, echoing the GOE's oxygen flood but with silicon instead of cyanobacteria. DARPA and FDA know: centralized MDs push Big Pharma TRT, but my tribe rebuilds the network—sun-gaze at dawn, ground to earth, ditch the blue devil. Humanity's young bucks aren't broken; they're optically orphaned. Reclaim the 380 nm key, restore NO's whisper to POMC, flood mitochondria with cholesterol via real light, and watch testosterone roar back. The GOE taught us adaptation; MKULTRA's sequel demands revolution.The implications? This is the Danny Jones podcast on steroids, your low T isn't lifestyle; it's light warfare. Tune your mito network, or stay a lemming.
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2. Biophotons Aren't Just Light, They're Spin's Secret Code, and Your Cells Are Hacking It. Forget the fairy tale that light's just waves crashing blindly into your biology. Biophotons? These ultra-weak glows from your cells carry spin—quantum angular momentum twisting left or right like a cosmic screw. When they slam into chiral proteins (those handed molecules twisting your DNA, enzymes, and muscle fibers), the helicity match decides: ignition or blackout. Right-handed photon vibes with a right-handed protein? Boom, exciton fireworks, energy zipping through photosynthetic factories or neural nets like greased lightning. Mismatch? The signal ghosts, lost in the ether, entropy's quiet win.This isn't woo-woo; it's the CISS effect (Chiral-Induced Spin Selectivity) in savage action, spin-polarized electrons or photons playing favorites with chiral structures, flipping biology's switches with ruthless precision. In photosynthesis, spin dynamics herd excitons (those delocalized energy packets) through protein mazes, quantum-coherent and efficient as hell, nature's way of outrunning the second law. Match the protein's symmetry? Trigger excitation, release the exciton floodgates. Fuck it up? Signal dissipates, nature's veto on bad code. Why does this gut-punch matter? Your body is this spin orchestra. Mitochondria, nerves, immune squads, all chiral battlegrounds where biophotons encode selective comms, shielding against chaos or amplifying it. Blue light nnEMF? They scramble spins, mismatch helicities, spike éR, your cells' desperate reroutes into inflammation, fatigue, entropy dumps. Sunlight? Full-spectrum spin symphony, syncing your quantum gears for peak flow.This is evolution's edge: Spin as the hidden hand, probabilistically tweaking mutations, energy transfers, even magnetochiral tricks in your veins. Centralized science chases genes; decentralized truth? It's spin's whisper in the light. Dive in, or stay mismatched. Your cells don't lie, do you? Stare at the sun. Ground. Hydrate. Ditch the jammers. Hack the helix. Share if your spin's aligned.
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You inject a jab kid gets a fever the retards in the office are instructed by algorithm tied to "evidence based protocols set by hospitals" to give tylenol. Retards giving tylenol are not taught that tylenol ruins CYP systems and this ruins glutathione signal which clears the heavy metals along with melanin. Since most infants have not been outside yet to build up the melanin system, they rely on the glutathione system for protection. And people wonder why healthcare is the leading cause of damage to your health. You cannot make this incompetence up because it is designed to harm. Decentralized medicine has the answers you all need. Savages pay attention Kevin's history lesson. Does tylenol cause anemia since it affect gluthathione recycling in humans? Yep. A small portion is converted into a toxic byproduct called NAPQI. Normally, this is neutralized by glutathione and safely excreted. Overdose and toxicity: In an overdose, the normal metabolic pathways become saturated, leading to a large amount of toxic NAPQI being produced. This rapidly depletes the body's glutathione stores. Oxidative stress: Without enough glutathione to neutralize it, the excess NAPQI causes oxidative stress, which damages cells, including red blood cells. RBC is how UPEs are delivered to the brain for development. 20% of cardiac output goes to the brain. ---> https://threadreaderapp.com/thread/1970240692053323803.html
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Australian Carnivores are getting ready to be loaded with GMO technology from their meat supply. This will add many atoms to their bodies to ruin cellular biology. On August 4, 2025, Meat & Livestock Australia (MLA) revealed it is partnering with Tiba Biotech and the NSW Government on a fast-tracked project to develop a world-first biodegradable mRNA vaccine for Foot-and-Mouth Disease (FMD). This vaccine has moved from concept to development in under 18 months, a fraction of the time traditional livestock vaccines take, with an initial spend of $2.5 million as part of a larger $20 million program jointly funded by MLA and the NSW Government. Australia is still FMD-free, but this is a big shift. For the first time, synthetic mRNA technology is being trialled in animals that Aussies eat. Where did this come from and why? Google Science and DARPA. I am issuing a stark warning: our fixation on the distant specter of Artificial General Intelligence is a dangerous distraction today. The real, world-altering disruption is already here, moving at lightning speed while we await a singular event. The chess game is over. The new, infinitely more consequential game is Protein Folding. Right now, the DoD is using vaccines and fake food to get atoms inside of us to ruin signal fidelity. Soon, they will use light in your environment to do this with quantum precision. They will use their new AlphaFold 3 algorithm to do it for you. This is an AI model from Google DeepMind that predicts 3D structures of biomolecular complexes, including proteins, DNA, RNA, ligands, and ions. This is a next-gen weapon that will be used to control all those who complied with the jab. Why? All those people now have intercalated DNA missense mutations this program will target. Google already can alter the light in your environment without your consent. They do this with indoor lighting, tech screens, and your email color temperature. Their terms of service give them this power, and you complied with it. You have no idea what POWER you gave them. And with their new AlphaFold 3 program, humans just been checkmated. Think of proteins not as biology, but as the universe's ultimate nano-machinery: copying machines, scissors, shears, engines, lights. All are built from a linear code of amino acids that crumples into a 3D object with a function. For decades, predicting that fold from the code was one of science's grandest challenges. Redox chemistry in cells controls this. Now Google has figured out how to control redox chemistry using light to refold the semiconductors that make up your life. This is what is happening in the Peptide space as well.
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In 1949 Dr. Antonio Moniz received the Nobel Prize for medicine, for invention the lobotomy procedure. There's a difference between an open mind and an empty head. Moniz work should have never been credited with a Nobel Prize considering the aftermath of what this tsunami wave created in medicine. If we teach only the findings and products of science – no matter how useful and even inspiring they may be – without communicating its critical method, how can the average person possibly distinguish science from pseudoscience? Bill Gates, WHO, WEF, Dr Fauci, Redfield, and Birks are the latest version of Dr. Moniz. If you thought that scene in 'Sucker Punch' where the doctor gave lobotomies with an ice pick was artistic exaggeration -- well, it wasn't. That's exactly how Walter Freeman, a popularizer of lobotomies in the 1940s, performed thousands of operations. He even trained non MDs to do them and invited the press to watch who often favorable covered these gruesome outcomes. Sounds like a familiar game plan done during COVID, doesn't it? Freeman executed Moniz operations. In fact, did you know, John F. Kennedy's sister Rosemary got a lobotomy from Freeman, which left her a vegetable for the rest of her life? And she was one of many people whose "cure" was more like zombification than freedom from mental anguish. @NicoleShanahan Pseudoscience is like a virus. At low levels, it's no big deal, but when it reaches a certain threshold it becomes capable of committing atrocities on the public health. The now-discredited procedure of the lobotomy, involves severing nerve connections within the orbital frontal gyrus from the rest of the brain of a mentally ill person. Many have called for this Nobel Prize to be rescinded now but science rarely repairs its errors. The removal of this Nobel still has not been done by "the centralized science experts" In 1949, giving the Nobel Prize for medicine to this procedure cemented that bad behavior in science was tolerable. After all, “The science was settled by giving this prize in 1949.” This sounds like the experts today in the WHO, GATES FOUNDATION, WEF, CDC, FDA, does it not?? Hundreds of thousands of lives were destroyed with this cruel unscientific procedure, with horrifying results. This is proof that Nobel Prize winning science is not always worthy of your trust.Remember the Nobel committee just gave mRNA technology a Nobel, proving again they are TONE deaf. Lack of the power to discriminate is no less evident in the sciences, namely in the tenacious life of false and refuted theories. Once these theories come into general credit in the literature, they continue to defy truth for centuries. The lobotomy operation is a reminder that one generation's Nobel Prize-winning cure is another generation's worst nightmare. The Nobel given for the mRNA technology is worse because it has killed and harmed many more people than the lobotomy did. Centralized scientists must be held accountable for their actions, and pseudoscience must be exposed and rejected. I am arguing that the centralized scientific community must learn from its mistakes and prioritize critical thinking and evidence-based research to prevent similar tragedies from occurring in the future. It appears Moniz's lobotomy lesson did not teach the NIH/CDC/FDA/NAIAD under Fauci one damn thing.
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We need to stop the techno tactic transhumanism in science. THIS IS WHY YOU EMIT A MAC ADDRESS!!👇 Imagine your own body broadcasting a digital fingerprint. With intrabody nanonetworks, tiny sensors and devices don’t just talk to each other through your skin and tissues—they emit a unique identifier, a MAC address, that can be recognized just like your phone or laptop on Wi-Fi or Bluetooth. This means your body itself becomes a living network hub, and that identifier could, in theory, be picked up by a nearby smartphone. What this paper reveals is that the human body is no longer just a biological system—it’s also a communication system, carrying its own built-in “address” for the digital world. Here is a breakdown of the PDF "IB-MAC: Transmission Latency-Aware MAC for Electro-Magnetic Intra-Body Communications" https://www.mdpi.com/1424-8220/19/2/341 --- What This Paper Is About The paper discusses Intra-Body Communication (IBC) – a technology where the human body itself acts as the medium for sending signals between wearable or implanted devices. Instead of relying on Wi-Fi or Bluetooth in the air, devices strapped to or embedded in your skin can send data using tiny electromagnetic waves that travel through your tissues. The authors propose a new communication protocol called IB-MAC. “MAC” here stands for Medium Access Control, which is the set of rules that determines when and how each device can talk without interfering with the others. Their protocol is designed specifically for the quirks of sending signals through the human body (like slower signal speed and slight delays). --- Why It Matters Reduced interference: Since signals stay mostly inside the body, they aren’t as easily jammed or eavesdropped on compared to normal wireless devices. Better for sensitive uses: Think military gear, hospital monitoring, or secure ID systems, where privacy and reliability are critical. More devices, less congestion: As we strap on smartwatches, medical sensors, fitness trackers, and AR headsets, regular Bluetooth gets crowded. Intrabody networks could ease that burden. --- How IB-MAC Works 1. Central “Coordinator” Node One device (like a central hub on the body) acts as the “traffic cop.” It assigns time slots for each device to send data. 2. Time Division Multiple Access (TDMA) Devices take turns speaking in pre-set slots, avoiding overlap. The protocol adds “guard times” (small pauses) to account for the fact that signals travel slower in the body than in air. 3. Superframe Structure Each communication cycle has three stages: Schedule phase: The coordinator tells each device its slot. Join phase: New devices can request to join. Data phase: Actual data (like heart rate, motion data, or video streams) gets sent. --- Key Findings Data Speeds: IB-MAC can reach ~452 kbps reliably (good enough for health data, even video in some cases). Latency: About 18–25 milliseconds – fast enough for real-time monitoring. Power Efficiency: Devices only need to keep radios on part-time, saving battery life. --- The MAC Address Angle Just like your phone or laptop has a MAC address (a unique digital “license plate” that identifies it on Wi-Fi or Bluetooth), intrabody devices using IB-MAC also assign IDs to each node. Each sensor (like a patch or implant) is given an 8-bit identifier so the coordinator can tell who’s who. These identifiers function like mini MAC addresses inside the body, letting the network organize dozens of devices at once. This means a person’s body network could broadcast a recognizable digital fingerprint, linking their wearable/implantable devices together. --- Why the Public Should Care This paper shows that our bodies can become living communication networks, with devices talking internally and outwardly in ways similar to how Wi-Fi works. That also means each person could be carrying an intrabody “address” – essentially a MAC address – that could identify or authenticate them in digital world
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2. This opens doors for: Healthcare: Continuous monitoring of vitals, smart drug delivery patches. Defense/security: Body-based secure communications for soldiers. Consumer tech: Seamless AR/VR or fitness systems. But it also raises privacy concerns, since these identifiers could, in theory, be tracked if someone could pick up the signals. --- ✅ In short: This paper introduces a trans humanist ideology to coordinate signals inside the human body so wearable and implantable devices that don’t interfere for the data collectors. It highlights that intrabody networks don’t just transmit data – they can also emit unique identifiers (like MAC addresses), effectively turning the body into its own digital network hub. - this is not science.
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Few know that the Federal Reserve Act of 1913 defies Article 1, Section 8, Paragraph 5 of the United States Constitution by creating a "central bank of issue" for the United States. Even fewer know that the Federal Reserve Act was written in secret by the Eastern bankers . It was a conspiracy among Paul Warburg, Edward Mandell House, Woodrow Wilson, J.P. Morgan, Benjamin Strong, Otto Kahn, the Rockefeller family, the Rothschild family, Harriman family and other European and American bankers that led to the founding of the U.S. Federal Reserve System. The Fed is not Federal and it has no Reserves. It is a private corporation that exists to collect usury from Americans. This is why Powell said no Trump can fuck off if he attempts to fire him. Know your history of how the Fed is organized by Paul Warburg who wrote the charters for the Fed in 1907-1913. Read Paragraph one below.
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2. Few realize that World War I, the Agricultural Depression of 1920, and the Great Depression of 1929 were brought about by international banking interests in NY and London to profit from conflict and economic instability. One just has to look to the Federalist Papers of Thomas Jefferson to see his staunch opposition to the establishment of a central bank in the United States. in 1913 the architect Warburg used Kuhn, Loeb & Co. and the House of Morgan for fronts for the Rothschilds/Rockefeller scheme. History now shows clearly that their were financial interests connected to the J. Henry Schroder Company and the Dulles brothers who helped facilitate the financing of Adolf Hitler by the Rothschilds and Rockefeller in an eloboarte plot to regain the allodial title of the USSR and USA. Hitler disdained international finance but he was convinced by the Royals, specifically Edward VIII to take the money from his bankers. The 1933 Concordant with the Popes was part of this plan. The Rothschilds/Rockefellers remain even today "world monopolists" and today modern globalists who have intercallted into the WEF/WHO/UN/NATO. The Rockefellers and City of London bankers own the Federal Reserve, because with some forensic accounting work you can see they own much of the stock of its member banks. BlockRock is now their proxy. If you trace stock ownership, as it changed hands via mergers and acquisitions, from the inception of the Federal Reserve in 1913 to the early 1980s you'll see it all in plain sight.
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3. Learn about Nelson Aldrich. He led the passage of the Aldrich–Vreeland Act, which established the National Monetary Commission to study the causes of the Panic of 1907. He served as chair of that commission, which drew up the Aldrich Plan as a basis for a reform of the financial regulatory system. The Aldrich Plan strongly influenced the Federal Reserve Act of 1913, which established the Federal Reserve System. Aldrich also sponsored the Sixteenth Amendment, which allowed for a direct federal income tax. the SCOTUS DECISION HOWEVER CLEARLY STATES THE 16th AMENDMENT ALLOWS FOR NO NEW TAX. IT NEEDS TO SCOTUS CHALLENGE NOW. OR MAYBE DJT HAS A PLAN? Aldrich, history books tells us, was deeply committed to the efficiency model of the Progressive Era, he believed that his financial and trade policies would lead to greater efficiency. Reformers, however, denounced him as representative of the evils of big business. His daughter Abigail married American financer John Davison Rockefeller Jr. who was the son of Standard Oil co-founder John D. Rockefeller. John Rockefeller famously told Congress during the break up of Standard Oil that he would make sure his actions from this day forward would bankrupt America. Well with the Fed and his creation of BigHarma he now sounds like a prophet. His descendants, including namesake Nelson A. Rockefeller, became powerful figures in American politics and banking and are the key architects in modern globalism. If you bank at Chase you support his crimes.
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4. Aldrich had some interesting ideas that link to DJT admonitions over the last few weeks. Namely on tariffs. He became a partner in a large wholesale grocery firm and won election to the Rhode Island House of Representatives. He only served a single term in the United States House of Representatives before winning election to the Senate in RI. In the Senate, he helped to create an extensive system of tariffs that protected American factories and farms from foreign competition, and he was a cosponsor of the Payne–Aldrich Tariff Act. He also helped win Senate approval of the 1898 Treaty of Paris, which ended the Spanish–American War.
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5. Following the Panic of 1907, Aldrich took control as chairman of the Congressionally established National Monetary Commission. A proponent of Progressive Era themes of Efficiency and scientific expertise, he led a team of experts to study the European national banks. After his trip, he came to believe that Britain, Germany and France had much superior central banking systems. He worked with several key bankers and economists, including Paul Warburg, Abram Andrew, Frank A. Vanderlip, and Henry Davison, to design a plan for an American central bank in 1911. This work included a trip to Jekyll Island in 1910 to finalize the details of the federal reserve banking plan. In 1913 Woodrow Wilson signed into law the Federal Reserve Act patterned after Aldrich’s vision, creating the modern Federal Reserve System. Did you know, three key rich people who opposed Aldrich plans at Jekyll Island were all on the Titanic.
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@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
8. Anyone see this tweet in the last few days? Did you find it odd?
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9. I told ya' in several podcasts about Dr. Kurt Plotner. He was the SS MD who was found on the NY docks by Meyer Lansky and turned over the to the US military. What he told the ONI, OSS, and Lansky was relayed to all inteliigence agencies. This is where MKULTRA began. What did Lansky uncover for the USA and the zionists of the time? The Monarch program is based upon Illuminati and Nazi goals to create a Master race in part through genetics. The Illuminati and Nazis are synonyms for the people Nelson Aldrich worked with and for.
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10. Dr. Kurt Plötner participated in a series of research tasks involving human experimentation at the Dachau concentration camp during the Second World War II. These included participation in the malaria experiments of Claus Schilling, in which prisoners were injected with drugs at lethal doses. In 1944, he was given Dachau physician Sigmund Rascher's role as head of the "Department R" of the Ahnenerbe project for carrying out experimental work on living subjects. Plötner also administered the hallucinogen mescaline to Jews and Russian prisoners, watching them display schizophrenic and mental behavioral changes, as part of the Nazi search for a truth serum that could be employed as an aid in interrogations. It was also used initially for a mond control drug. It failed on both accounts. This information was captured by Lansky on the docks of NY harbor and given to Groves, MOSSAD, & Boris Pash. It is believed that Lansky was the famous NYC gangster that the CIA has admitted to below who actually participated early in MKUTLRA. Plötner's work in the concentration camps came to the attention of Boris Pash, an American intelligence officer who would go on to work in the CIA at the time of Operation BLUEBIRD/Artichoke in the 1940s. This document below was formerly classified document from 1952 on the CIA’s Project BLUEBIRD, an offshoot of Project MKULTRA which focused on hypnosis and behavior modification as a means of preventing Agency employees from providing intelligence to adversaries, was obtained from the CIA Freedom of Information Act Reading Room. Y'all do not know your history well enough for me. https://publicintelligence.net/cia-bluebird/
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11. Instead of treating him like a War Criminal, the United States Navy's intelligence officers recruited him in 1945, permitting him to continue his interrogation research for the new MKULTRA program in the USA. Plötner proceeded to live under the name of "Schmitt" in Schleswig-Holstein into the early 1950s. Despite Plötner's actual residence in this western German zone, when the French government sought to have Plötner prosecuted in 1946 and appealed to the United States for assistance, the Americans replied that he could not be located, and was probably being shielded by the Soviet Union. He subsequently was able to quietly resume his real identity in 1952, at which time he was hired by the University of Freiburg in West Germany. He became an associate professor in 1954. Plötner died on February 26, 1984.https://www.cia.gov/readingroom/docs/CIA-RDP81-00261R000300050005-3.pdf
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12. History books are written by the victors. But the diligent can still find the truth in their sea of lies.
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13. Investigative efforts around MKULTRA's real purposes were hampered by the fact that CIA Director Richard Helms ordered all MK-ULTRA files destroyed in 1973; Helms was intimately involved with William Casey in the Octopus program that began in the Carter administration and dominated the Reagan agenda. It manifested in the drug cartel connections to money laundering for CIA benefits of covert ops. The Church Committee tried to expose it, but the simultaneous Rockefeller Commission tried to keep most things in it COVERT. Investigations had to rely on the sworn testimony of direct participants and on the relatively small number of documents that survived Helms' destruction order. Although the CIA insists that MK-ULTRA-type experiments have been abandoned, 14-year CIA veteran Victor Marchetti has stated in various interviews that the CIA routinely conducts disinformation campaigns and that CIA mind control research continued. In a 1977 interview, Marchetti specifically called the CIA's claim that MK-ULTRA was abandoned a "cover story" perpetuated by the Rockefeller Commission. This is where the Brain Health Initiatives were born and placed in Central and South America with the help of the Volkow family in Mexico. Light and drugs used on the HPA axis were the core of their study. On the Senate floor in 1977, Senator Ted Kennedy said: The Deputy Director of the CIA revealed that over thirty universities and institutions were involved in an "extensive testing and experimentation" program which included covert drug tests on unwitting citizens "at all social levels, high and low, native Americans and foreign." Several of these tests involved the administration of LSD to "unwitting subjects in social situations." At least one death, that of Dr. Frank Olson, resulted from these activities. The Agency itself acknowledged that these tests made little scientific sense. The agents doing the monitoring were not qualified scientific observers. MKULTRA DESIGN WAS TO HURT PEOPLE BY CONTROLLING THEM The banking families who own the Fed. Rockefellers and Rothschilds.
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14. Everything I have done over the last 18 months is reflected here in this documentary. Watch it in total to understand what you have missed. Your life depends on it and the next 50 generations of your family is being sold into economic slavery. Why does DJT want to get rid of Income tax? That is the usuary that Paul Warburg got for the banking families in the Fed.
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15. Do your homework. https://aim4truth.org/2018/04/17/exposed-all-the-queens-agents-and-corporations-that-control-the-world/
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16. The extra mile is a vast, unpopulated wasteland where the Black Swan mitochondriac goes. People say they go the extra mile, but almost no one actually does. Most people think, "Wait, no one else is here. Why am I doing this?" The Black Swan is rare because their mindset is unique. That's why the extra mile is such a lonely place for the common man. That's also why the extra mile is a place filled with opportunities and time expansion. Be early. Stay late. Make the extra phone call. Send the extra email. Do the extra research. Know the history help human thrive. Help a person solve a difficult problem. Help a customer unload or unpack a shipment. Don't wait to be asked for help; offer. Every time you do something, think of one extra thing you can do--especially if other people aren't doing that one thing. In this unpopulated wasteland, many will ask you why you persist. Tell them your using nature's light to sculpt your life by thinking better than you did before. Sure, it's hard, to think anew and adapt. Being solo in the modern world is not something to fear........it is something to conquer. I been doing it for 20 years. But that's what will make you different and unique--and over time, it will make you incredibly successful when you begin to write your next chapter. It will be a book all will want to read when the see the words of your story spill all over the pages...........
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17. For those of you who do not know what happened between the MKULTRA Program from 1953-1964 then transferred to Stanford Reseach Insitute in 1946-2013 and finnally to the 2013 Brain Health Initiative of Barry Obama Here is what Clinton copped to in 1995. Why did Jeffrey have this over his mantle. Connecting any dots? Awake yet?
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@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
19. If you listened to the Danny Jones Podcast I did you'll hear about who partook in the Marshmallow experiment as a children. Esther Wojcicki the mother of Susan and Anne and the former Mother in law of Sergey Brin set it up for all the future Big Tech leaders to go through at SRI. Dr Kruse mentioned various big tech folks being part of this experiment when they were children. How would we find out who else was experimented on? Subpena the criminals and go through their records. You'll find that Marshmallow and Asch experiements all came from Monarch and the Nazis. I see where all the pieces fit, do you? https://www.youtube.com/watch?v=MM62wjLrgmA
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@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
21. Dr. Sidney Gottlieb got the Eisenhower administration approval of an MKULTRA sub-project on LSD in this lone 1953 letter left remaining after the MKULTRA destruction order. Division, followed by the word ULTRA (which had previously been used to designate the most secret classification of World War II intelligence). Other related cryptonyrns include MK-NAOMI and MK-DELTA. A precursor of the MK-ULTRA program began in 1945 when the Joint Intelligence Objectives Agency was established and given direct responsibility for Operation Paperclip. Operation Paperclip was a program to recruit former Nazi scientists and this began before end of WW2 when General Groves had Meyer Lansky patrol NY docks for U boat spies in NY harbor. Some of these scientists studied torture and brainwashing, and several had just been identified and prosecuted as war criminals during the Nuremberg Trials. Several secret U.S. government projects grew out of Operation Paperclip. These projects included Project CIIATTER (established 1947 by Groves/Kennan), and Project BLUEBIRD (established 1950 by Kennan), which was later renamed to Project ARTICHOKE in 1951. ARTICHOKE contained used of cryptography in its program. Lansky was involved in this. Here he learned about puberty blocking drugs used on Turing by MI6. Project CIIATTER is where Lansky's prisoner he caught on docks in Brooklyn wound up. This is where alien light frequencies were begun to be used in interegations. CIIATTER is where ritual abuse was also studied. Many of the extremes in electromagnetic abuse was linked to gender changes, hormone modulation and was associated with extreme abuse survivors, dissociation of identity/geneder, traumagenic amnesia/PTSD, loss of self-regulation, autonomy, quality of life. Lansky began the pedo and sex rings to ensnare corupt US politicians for the MOSSAD. The big fish that he got? J Edgar Hoover. He also caught JFK and RFK Sr and Marilyn Monroe. That ring he built for the MOSSAD was eventually taken over by Epstein and Ms. Maxwell and it caugth both Bush's, Bill Clinton, Hillary, Abedein, Weiner, Harvery Weinstein, Obama and his spouse, and Oprah. What is their goal? What hat do they wear?
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22. The uses of 435-465 nm light makes the mind suceptible to propaganda by creating false Memories – The Deception That Silenced Millions, Lynn Crook. This program created child molesters, FMSF, extreme child abuse, sadistic sexual abuse, ritualistic abuse, mind control, torture. Many of them were funneled into Lansky's pedo/sex rings used to blckmail politicians. J. Edgar Hoover gets clipped by Lansky in this program. Most of this behavior is eventually found in the transhumanist community years later as their children inherent this abuse transepigenetically. This was unknown prior to this Project in the CIA. Ritual Abuse and Mind Control was then placed in Art and Literature by CIA to see effects in public. this mimicked the drugs they unleashed in the population at the same time. Light abuse inducing stress was more reliable than drug use. This art work was owned by industrial miliatry complex by way of Lansky's money movement skills and it was made expensive by the people grommed in CIIATTER who were placed in the art and music industries by the CIA. See Lynn Brunet PhD, Freemasonic themes, trauma covered in her case studies. This was also resonated in Carl Jung’s Red Book, Masonic rites, Masonic ritual abuse, fraternal initiation rites, complex trauma, survival skills seen in many industrial military complex CEOs. Corporations and academia were filled with these people by the CIA. Their purpose was to study mind-control, interrogation, behavior modification and related topics were headed by Dr. Sidney Gottlieb, the MK-ULTRA project was started on the order of CIA director Allen Dulles on April 13, 1953, largely in response to experiments by Mob in Vegas casinos linked to Bugsy Seigel hit, the Soviet, Chinese, and North Korean use of mind-control techniques on U.S. prisoners of war in Korea in the 1950s. The CIA wanted to use similar methods on their own captives but they found light was the most rapid and reliable way to alter behavior via dopamine and melatonin alterations. The CIA was also interested in being able to manipulate foreign leaders with such techniques and would later invent several schemes to drug Fidel Castro using tobacco, drugs, and SV40. Experiments were often conducted without the subjects' knowledge or consent" In some cases, academic researchers being funded through grants from CIA front organizations were unaware that their work was being used for these purposes. See Alton Ochsner and Carlos Delgado in the 1950s-1960s. In 1964, post JFK heat, the project was renamed MK-SEARCII. @JonesDanny Awake yet?
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23. The project attempted to produce a perfect truth light and drug use for use in interrogating suspected Soviet spies during the Cold War, and generally to explore any other possibilities of mind control. Sidney Gottlieb Another MK-ULTRA effort, Subproject 54, was the Navy's top secret "Perfect Concussion" program which used light to induce TBI. This is where Havana Syndrome was FIRST discovered using microwaves was studied which used sub-aural frequency blasts to erase memory by affecting frontal/temporal lobe loops which have melanin and cochlear melanin. Because most MK-ULTRA records were deliberately destroyed in 1973 by order of then CIA Director Richard Helms before Senator Church's subpena's, it has been difficult, if not impossible, for investigators to gain a complete understanding of the more than 150 individually funded research sub-projects sponsored by MK-ULTRA and related CIA 171 programs. Most of these were folded into DARPA in 1965 and were used in many other intelligence covert programs in the 1970s that morphed into Project Octopus. Octopus is where hijacking of the beta endorphin pathway by opiates was exploited. Later it morphed and evolved into the Brain Health Initiative in 2013. It was moved offshore to Central and South America because of provisions in the Patriot Act which were problematic. Google's Brin and his ex wife Wojcicki are the current poster children of these programs. Her board just quit enmass on her when they heard her "new plans" for data theft. Did you know she trained the Means Sibling with an MD? Yeah the one who went to Stanford who quit her chief year of her ENT residecy to start a WBAN IOthings company. Guess where she got that idea? She wants us to believe Fruit loops and McDonald's kills us.......even Morgan Spurlock told us she is a psy-ops put in by the opposition to run the Hegalian Dialect.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
24. Israel is a creation of fiat currency and central banking. This is why Israel is protected by the Industrial military complex of the USA. The Rockefellers and Rothschilds linked directly to the Balfour declaration and most of you have ZERO idea it came directly from Queen Elizabeth's DAD on Novemeber 2, 1917 during a World War. The Zionist are the bankers in the UK and USA and in the Papacy. That was the whole point of the Mondriatt Concordant of 1933 and why Hitler was raised to sent German Jews to Palestine to raise the population from 3% to 90%. It was designed to be a land sink for Jews. The problem became complicates as Hitler became overwhelmed with the process from 1933-40 and he got no help from the people who set up the process: The Rothschilds and Rockefellers. He morphed from stealing assets and transfering people the bankers wanted to Palestine. This was their Final Solution to alter the population imbalance in Palestine at the time. People forget Palestine was a British colony back then. When Hitler decided to eliminate people instead of shipping them to the promise land, this move surprised the bankers and then curbed his abilities by tilting the War table financial. War and Imperialism is a function of Central Banking. This defines Israel's history with the Balfour declaration. Not even smart Bitcoiners who are Palestinian see it fully due to ideologic cognitive bias of their ancestory. I have no blinders. Banking is at the core of our sickness https://www.youtube.com/watch?v=6SPnD9819CU
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
26. What is happening right now. Lutnick is a dual passport guy who magically missed the planes in 9/11 or at least that is how the story goes.........
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
27. Purpose? It is being done to get the Royals and Pope back to their relative positions of where they were in Medival Europe. Dominant power.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
28. Those who make the rules control the money = Bitcoin fixes everything. All DJT has to do is get one thing right. Will he?
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
29. The DJT transition team is being infiltrated by traitors in case they do win and the Harris Steal team does not pull off the "Immaculate election." I called out the entire CABAL today. Bobby needs to be aware that the people who killed his Uncle and Dad are now trying to get inside his circle. As @Fynnderella1 said on her podcast with Mike, That must stop. https://threadreaderapp.com/thread/1852450070085439679.html
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
30. Your enemy is usury charge on money or loan caused by the bankers in the Fed and BoE. World War I was caused by finance capitalism, called "usury. Many wrote books on the above topics in the 1930-50s above but could not get it published because of how they called out the Rothschild's and Rockefeller's monopoly game. Youre being lied too. Know that bigHarma sits closer to the money printer than anyone. Know your enemies are inside the gates.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
31. Remember that the centralized PEER review is run by the heirs of Robert Maxwell. His daughter is in jail in the USA protecting the Zionist federation bankers and technologists in this thread. They are loyals to the Royal Family and Popes via their bankers. Maxwell was a primary actor in the MEGA Group. How much do you know about them? Epstein had deep ties to Israeli intelligence and has well-documented ties to influential Israeli politicians and the Mega Group. Those guys are layered links of the MOSSAD and to Meyer Lansky. Ronald Lauder a cosmetic heir who makes billions blocking women from the sun is a Mega Group member. He has known Trump now close to 60 years. He is also very tight with Ms. Wiles. He is a former member of the Reagan administration and a long-time donor to Israeli Prime Minister Benjamin Netanyahu. He is very influential in Israel’s Likud Party. He was a long time friend of lawyer Roy Cohn. Robert Kennedy Sr. was Cohn assistant to Senator Joe McCarthy in the 1950s during Eisenhower's administration. Be aware of it all and pay attention to what happens in the Belt way. Are they working for us or not. If not let's get rid of them too. Did you know that Lansky was involved funding math research of Turing from 1969 to 1983 working on cryptography and that work linked art sales and money laundering through the IRS and Treasury via infiltration of the Executive branch. This work set the stage for the Iran Contra money Laundering schemes that linked the MOSSAD to Executive Branch. Can you guess what else it linked too?
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
The real bombshell isn’t that Epstein ran a trafficking ring. It’s that he was allowed to operate it because bankers like JP Morgan's Jamie Dimon was complicit in this and people would begin to ask how and why Bankers and the Treasury allowed this given the 1970 Bank Secracy Act. The billionaires are not the architects of this information terrorist networks. They’re the actors in the play. Elon. Thiel. Gates. Adam Back, Saylor. Lutnick, His Son They run infrastructure, but they don’t own the world. They were groomed, by systems older than corporations. The real owners? The Royals, The Grey Pope, BlackRock, Vanguard, BIS — own the assets The Vatican, Rockefeller, Rothschild, DuPont — own the timeline The WEF, CFR, Chatham House — write the scripts Political Think tanks + foundations — enforce ideology Occult orders + Straussian elites — justify it all as “destiny” This is not capitalism. This is a technocratic theocracy, where power is hidden in these information terror networks, in their algorithms, law, debt, and narrative. They don’t fear elections. They fear recognition by the masses. Elon Musk was deposed in the trial that bank issue was dealt with as well. Then there is the issue of why the number one dealer broker in the USA who ran Cantor Fitzgerald who interacts with the Treasury Dept and the bankers (Lutnick). He was the next door neighbor of Epstein and that he did business with him. Epstein was running this sex surveillance business on behalf of the British Zionists, The Royal Family, The Vatican, intelligence agencies, mostly likely elements of the CIA, MI6 and Mossad in some capacity. The family Maxwell links the British Crown to Centralized Science and PEER review. Ghislaine Maxwell’s father, Robert Maxwell own most of the PEER infrastructure controlled by scientists who are controlled opposition, so what is published in journals supports a narrative the elite foster and want. Moreover, Robert Maxwell, was a known Israeli asset as well as a Soviet asset. This is information terrorism for the 21st century, except instead of bombs in train stations, the payload is child rape footage used to control Presidents, bankers, entertainers, intelligence agencies and many CEOs (Victoria Secret and Abercrombie & Fitch).
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
2. Epstein's link to Centralized Science will also link him to cryptography. Few.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
3. The Mindshift Conference, hosted by Jeffrey Epstein and organized by Al Seckel, took place in early January 2011 on Epstein’s private island, Little Saint James, and in Saint Thomas, U.S. Virgin Islands. It covered topics including artificial intelligence, complexity theory, new trends in theoretical physics, evolutionary biology, cognitive neuroscience, minimally invasive surgery, encryption and decryption, new financial systems, and emerging technologies like crypto currency and quantum computing. Steven Pinker and Larry Krauss were there. So was many JP Morgan and Google executives. Jeffrey Epstein used his good friend Joichu Ito’s Digital Garage firm to help fund crypto, AI and biotech startups including Adam Back’s Blockstream. Joichu Ito was the director of MIT Media Labs, responsible for incubating many crypto related projects with connections to futurist proponents like Reid Hoffman. The NSA and CIA have a history of recruiting assets from MIT and Stanford, where most of these people are alumni. Hoffman was a funder of Adam Back’s Blockstream and board member, as well as being a board member at: MIT Media Labs, Microsoft, OpenAI, and Mozilla. He was VP at PayPal and a PayPal mafia member, and founded LinkedIn. Coincidentally or not, Satoshi Nakamoto was “born” one day after the founding date of Microsoft. Microsoft has longstanding ties to the US governemnt, including the NSA and DARPA.
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4. The Extropy Institute, co-founded by Max More and Tom Bell in 1991, was a non-profit organization promoting extropianism, a transhumanist philosophy advocating for indefinite life extension through science and technology, uniting thinkers in AI, nanotechnology, and cryonics, before closing in 2006, declaring its mission "essentially completed. Important members of Extropy included: Hal Finney, Nick Szabo, Max More, Eliezer Yudkowsky, Jaron Lanier, Nick Bostrom, Marvin Minsky, Ray Kurzweil, Steve Jurvetson, Ralph Merkle, Todd Huffman, Greg Burch and Julian Assange. The Edge Foundation, founded by John Brockman in 1998, is an intellectual salon hosting discussions among scientists, technologists, and thinkers to explore cutting-edge ideas, primarily through its website, http://Edge.org, and annual events like the Billionaires’ Dinner. The Edge organization received significant funding from Jeffrey Epstein, who donated $638,000 of $857,000 total from 2001 to 2017, often as the sole donor in some years, with Epstein’s financial ties to Brockman dating back to 1995. Notable members include evolutionary psychologist John Tooby, physicist Freeman Dyson, cognitive scientist Steven Pinker, and tech entrepreneurs like Jeff Bezos and Elon Musk, with Peter Thiel also linked through board membership and event attendance. You should all know this. This is why Elon was deposed in the JP Morgan trial. You should know that Amazon now has a space and satellite division and that that Howie Lutnick is linked to this too. And why is Bezos important? It links Space surveillance to healthcare DARPA projects done by his ancestors.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
5. Other members of Edge besides Epstein, Musk, Thiel and Bezos includes: Nick Bostrom, Marvin Minsky, Ray Kurzweil, Steve Jurvetson (who helps fund all of Elon Musk’s companies), Vinod Khosla, George Church (Epstein funded futurist scientist), Larry Page and Sergey Brin of Google, Paul Allen and Bill Gates of Microsoft, Jeffrey Epstein’s good friend Joichu Ito, and Yuval Noah Harari. Many of the people listed above in these three foundations are members in at least two or all of these foundations, considering they all have similar themes (transhumanism and futurism). Coincidentally, all three foundations have funding and membership from Jeffrey Epstein. Several of the people listed who are members of either one or more of these futurist foundations are also cypherpunks. Cypherpunks are a group of activists and cryptographers, formed in the early 1990s through an email list, advocating for privacy and individual freedom through strong cryptography and decentralized technologies. their ideas influenced Bitcoin and projects like WikiLeaks. They focused on tools like PGP encryption and anonymous remailers to counter government surveillance. Some of those early cypherpunks include: Julian Assange, Adam Back, Hal Finney, Nick Szabo, and Todd Huffman. Savages might want to remember this when my Podcast with @BTC_Archive goes live.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
6. Alcor Life Extension, Humanity+, Methuselah Foundation The Alcor Life Extension Foundation, founded in 1972 by Fred and Linda Chamberlain in Scottsdale, Arizona, is a nonprofit pioneering cryonics, preserving human bodies or brains in liquid nitrogen after legal death, hoping future technology can revive them. As of October 2023, it has 1,927 members and 222 cryopreserved patients, though cryonics remains controversial and scientifically unproven. Notable members include Peter Thiel, who is signed up for cryopreservation. Peter Thiel has a strong interest in life extension, funding anti-aging research through his Thiel Foundation, including $7 million to the Methuselah Foundation and investments in Unity Biotechnology. He has explored controversial methods like parabiosis, linked to Ambrosia, a startup offering young blood transfusions for $8,000. Marvin Minsky, a longtime AI and transhuman enthusiast is also a member of Alcor. Other people mentioned earlier in this thread who are also members of Alcor, as well as Lifeboat Foundation, Edge Foundation or Extropy Institute include: Jeffrey Epstein, Max More, Hal Finney, Ray Kurzweil and Todd Huffman. Humanity+, formerly the World Transhumanist Association, is a nonprofit founded in 1998 by Nick Bostrom and David Pearce to advocate for ethical use of technology to enhance human capabilities, focusing on longevity, AI, and genetic engineering. Jeffrey Epstein donated at least $120,000 to Humanity+, the largest amount they recieved from a single donor, with other donors giving much smaller amounts. Noteable members include: Nick Bostrom, Ben Goertzel (who received direct funding from Epstein through the Jeffrey Epstein VI Fund for OpenCog), Todd Huffman, Max More, Patri Friedman, Aubrey De Grey and Wei Sun. Patri Friedman is the founder of Pronomos Capital which was funded by Peter Thiel. The Methuselah Foundation, co-founded by David Gobel and Aubrey de Grey in 2001 in Springfield, Virginia, is a nonprofit dedicated to extending healthy human lifespan through regenerative medicine and tissue engineering, with a mission to "make 90 the new 50 by 2030." It funds research, incubates startups via its Methuselah Fund, and sponsors prizes like the Methuselah Mouse Prize to advance longevity science. Notable supporters include Peter Thiel, who pledged $3.5 million in 2006, and Vitalik Buterin, who donated 43% of Dogelon Mars cryptocurrency to the foundation.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
7. The most shocking thing is you should know shitcoiner Buterin is now funding one of the scientists at the core of the contaminated COVID jabs. I have a sense he knows he is GMO and needs to solution to a problem now. Many new problems in the NEW jabs seem to be in the old ones too.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
8. Many early Bitcoin and crypto pioneers have ties to intelligence agencies and some of those ties get awfully close to Robert Maxwell and the PROMIS software scandal tied to Israel’s 8200 Unit. This software was key because it had a backdoor built into it that Meyer Lansky IT team used to have the inside scoop on governments. This backdoor idea for many algorithms became an intelligence story due to Maxwell's success with PROMIS. It was used in the Octopus Murders during the Reagan and Bush years. Several of the early cypherpunk and libertarian assets became tied to the Bitcoin story as “whistle-blowers” against the US government. They are not who you think they are either. In the beginning of installing the surveillance state they became modern day Lee Harvery Oswalds and now are playing roles to give the illusion of brave heroes going against the machine or “big brother”. These whistle-blowers include Julian Assange, Chelsea Manning and Edward Snowden. Edward Snowden, famously leaked thousands of classified documents including the global surveillence program, inlcuding PRISM, was a former contractor for Booz Allen Hamilton. CALLEY MEANS WORKED for Booz Allen, as I exposed on Danny Jones. This is not a coincidence. Booz Allen Hamilton, is a major U.S. government contractor, has deep ties to the CIA and broader intelligence community, employing over 1,000 former intelligence officers and securing $1.3 billion in intelligence contracts annually as of 2013. Snowden held positions in both the CIA and NSA. He is assocaited (or was) with several relevant cypherpunks, including Moxie Marlinspike, Jacob Appelbaum, Runa Sandvik and several others. Intelligence has tried to infiltrate Bitcoin long ago but to date they have failed badly.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
9. Julian Assange was a member of the Extropy Institute. Chelsea Manning, a former U.S. Army intelligence analyst, leaked over 700,000 classified documents to WikiLeaks in 2010. He then orchestrated the release of U.S. military and diplomatic leaks, including the Iraq and Afghanistan war logs, sparking global controversy. Coincidentally, Chelsea manning (a transgender male to female) once dated Elon Musk’s ex “Grimes” (Claire Boucher) [likely also a transgender male to female]. Chelsea Manning was also close with cypherpunks like Isis Lovecruft and Yan Zhu. Yan Zhu was an intelligence analyst for the US DoD, as well as a ‘Hacker Comununity Organizer’ for Noisebridge, a “hackerspace” noteable in the cypherpunk community. Yan Zhu was also a member of the Electronic Frontier Foundation. The Electronic Frontier Foundation (EFF) is a nonprofit organization dedicated to defending digital privacy, free speech, and innovation through litigation, policy advocacy, and technology development. Noteable members of the EFF include: Hal Finney, Jacob Appelbaum, Yan Zhu and Esther Dyson. Esther Dyson worked closley with many transhumanist and cypherpunks. She also worked with Barney Pell of Singularity and Bing! (Microsoft) as well as received funding from Jeffrey Epstein for her research on transhuman and longevity science. She worked at Space Adventures with XPRIZE founder Peter Diamandis. Diamandis also is a member of Singularity with Barney Pell, Ray Kurzweil, David Bray and Cathie Wood. Cathie Wood funds many Elon companies and Peter Thiel’s Palantir. Todd Huffman worked with the US DoDlike Yan Zhu, specializing in intelligence analysis. They also are both members of Noisebridge mentioned before, the “hackerspace” community event for cypherpunks. He also worked extensively with DARPA, helping found and operate the TOR Project. The Tor Project, founded in 2006 as a nonprofit, develops Tor, a free, open-source network that enables anonymous communication by routing internet traffic through multiple volunteer-operated servers to conceal users’ identities and locations. All of these people should never be trusted.
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10. I made the link for the world of TOR to Lansky via David Chaum on the @Breedlove podcast. This thread has a lot more juice I have not spilled.......but now that we know DOJ is burying the Epstein case it is time to out the traitors. Bondi and Wiles are running the inside game for the cabal.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
11. There is a reason Bitcoin Treasury companies are forming now and it is not what most Bitcoiners think. This explains why today the US government magically lost some of its Bitcoin. soon we will probably find out that Lutnick and Fink are collecting Bitcoin Assets offline and will control large poools of Bitcoin to make markets for the US government. This likely will be done to prop up the UST market. The Bitcoin likely will come from idiots who listen to people who are in Bitcoin Treasury positions who decide to custody bitcoin for some extra juice. SAVAGES should never fall for this scheme. Never trust Lutnick or Fink. Why? Read the first tweet and see who they really are. Lutnick and Fink will confiscate the bank if you lend your coins for leverage. 6102 EO is in the Genesis block for a reason folks.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
12. It is critical that I drive home two points to the SAVAGES: 1. CCP is $ETH's biggest whale, masked behind a guy named Wanxiang and others. This man is th enumber one reason that even though Biden admin has the same data on Epstein that Trump admin had in his first and second terms, Biden never mentioned Epstein once. The media is trying to blame DJT for the Epstein debacle but that is bad detective work. Wanxiang is why Operation Chokepoint 1.0 and 2.0 occurred and Gensler was forced to enforce it covertly. 2. Wanxiang was perfectly positioned to wear the Mask for the elites who want us back to Monarchy rule and one world government ideas buried in the real fabric of modern reality. HQ'd in Chicago, tied in deeply to Biden & Bush, Putin, and all the Space programs in Russia, USA, and EU. This is the blood and guts inside of Space Force. They have Blockchain Partnerships with MIT, IBM, UBS, Microsoft, and more. Wanxiang is how the worlds globalist are getting money and rare Earth metals out of North Korea to support the technocratic control agenda. ETHER is the honey pot for these criminals. This explains why anytime NK needs cash they easily hack an ETH whale.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
13. During the Obama and Biden Admins now you can see why the crypto and shitcoiner bros were controlling the SEC and Gensler. The CCP's Ethereum sway through Wanxiang is deeply concerning to Savages. Their ties in the US and SEC's approval warrant serious scrutiny by Bondi but she is captured CCP. It's essential to demand transparency in crypto dealings, especially when involving entities connected to authoritarian regimes. This perhaps well explains why North Korea easily hacks ETHER customers when it needs money for anything....... One way to get money out of North Korea is thru Wanxiang, the largest backer and funder of the Ethereum Foundation and over 500 crypto ICOs. Wanxiang, a communist China party connected company, is the #1 exporter of Uranium and rare Earths elements out of North Korea. They were also the backers of Prometheum, when the @SECGov gave them the ONLY Special Purpose Dealer Broker license for Digital Assets, opening up Americans most sensitive data to the #1 threat to our Democracy (outside of our own rogue Agencies). This means the Blue party is owned by the CCP and the Red Party has deeper ties to Bankers Controlling Israel and Wall Street - Rothschilds/Rockerfellers. Neither have control of Bitcoin which went open Source in the Chaum/Sassman Epoch. Their only methods of control of their lost currency is off and on ramps and via centralized confiscation or mining operations. Savages need to be mindful of all of this.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
14. China ties DEEP to Ethereum, Ripple, Stellar, Tron, BitTorrent + Connections surrounding Ethereum, Ripple, Stellar, Tron, BitTorrent and how they tie in with China. Anyone who shills these coins is a communist fascist who wants a WEF one world government. XRP and ETH are joined at the hip for this cabal. Both are bank accounts for the criminals. Vitalik Buterin: Vitalik Buterin, the co-founder of Ethereum, was awarded a Thiel Fellowship in 2014, a program initiated by Peter Thiel to support young entrepreneurs who skip or drop out of college to pursue innovative projects. Buterin received a $100,000 grant to focus on developing Ethereum. This fellowship provided financial and networking support leading to his 2013 White Paper of Ethereum. Palantir boss is the seed man. Prior to this, in 2012, Buterin sought employment with Ripple (XRP), a cryptocurrency company focused on payment solutions, and was offered a position by Ripple co-founder Jed McCaleb. He allegedly slept on David Schwartz’s couch, the CTO of Ripple, at the time he was trying to gain employment at Ripple. However, the opportunity fell through due to visa issues preventing Buterin from working in the United States. At the time Vitalik was viewed as a cryptographic spy under the Munitions Act. Biden Admin changed this status. Dorsey a bitcoin maxi has always pointed out this pathway to the CCP actively on Twitter to alert the savages to the real shitcoin alliance.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
15. Just who is Vitalik. He is Lee Harvery Oswald of the CCP. Vitalik co-founded a company with Peter Thiel’s Founders Fund partner Joey Krug called Augur. Vitalik is a member of the transhumanist/ futurist group, Lifeboat Foundation. He is currently funding some rather shocking names in the COVID space. I am withholding some of those connections for deep reasons. Who are other members and partners of Vitalik's Augur? They included Jeffrey Epstein, Charles Hoskinson of Cardano, Tammy Camp of Stronghold, JR Willet of Tether, Stuart Hoegner, lawyer for Bitfinex, and Stanislav Shalunov of BitTorrent (among many others). Vitalik is an advisor and co-founder of Fenbushi Capital. Many of these companies are tied to two famous podcasters that you all think works on your behalf. YOU'RE WRONG. Fenbushi Capital is the first and most active blockchain-focused venture capital firm in Asia, founded in Shanghai in 2015 by Bo Shen, Vitalik Buterin, Xiao Feng. KNOW YOUR ENEMIES, Savages
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
16. How filthy and deep are these links of Vitalik et al.? Some of Fenbushi’s investments include: Circle, ConsenSys, Securitize, O(1) Labs. ConsenSys is a blockchain technology company that specializes in building decentralized applications (DApps) and infrastructure for the Ethereum blockchain. It was founded by Joseph Lubin in 2014. Joseph Lubin is the co-founder of Ethereum. Securitize has lead funding by Ripple. O(1) Labs has funding from many leading Chinese venture companies. One of O(1) Labs’ advisors is Jill Carlson who was strategy lead at Inter/Stellar (Stellar subsidiary) from 2016-2017. One of Vitalik’s leading investments is in Starkware Industries, an Israeli software company that specializes in cryptography. It develops zero-knowledge proof technology that compresses information to address the scalability problem of the blockchain, and works on the Ethereum platform. Other investors include: Founders Fund, Sam Bankman-Fried, Joey Krug (co-founder of Vitalik’s Augur company), Tiger Global, Three Arrows Capital and many others. Uncle Jack is the modern day Gen Patton. He is letting you know how the CCP and folks in the desert really link behind the curtain. They have the same goals for one world government.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
17. Just how big was the Biden Admin connection to this criminal syndicate? Xiao Feng, Prometheum, Wanxiang, McCaleb + Vitalik Buterin of Ethereum is an advisor and co-founder of Fenbushi Capital. Fenbushi Capital is the first and most active blockchain-focused venture capital firm in Asia, founded in Shanghai in 2015 by Bo Shen, Vitalik Buterin, Xiao Feng. Fenbushi has ties to the Chinese government and likely the CCP more specifically. Xiao Feng (Feng Xiao) Feng Xiao is Founder of PlatON, Wanxiang Blockchain, Fenbushi Capital and Board Member of Prometheum. Prometheum, a crypto shitcoin company offering custody and trading services for digital assets, has sparked controversy due to its close relationship with the SEC. The company became the first to receive a special broker-dealer license for digital assets from the SEC, a decision that has drawn criticism from the crypto industry. Critics have labeled Prometheum an "SEC pet project," pointing to its approvals as evidence of potential favoritism, especially amid the SEC's broader crackdown on other crypto exchanges. The controversy intensified when Prometheum announced it would custody Ethereum (ETH) and classify it as a security—contradicting the Commodity Futures Trading Commission’s (CFTC) view that ETH is a commodity. This move fueled concerns about regulatory overreach and the potential impact on Ethereum’s classification and the wider crypto market. David Sacks links here in the crypto space are not GOOD for Savages. Same is true with Lummis. Neither are who you think they are.
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18. Additionally, lawmakers have raised questions about the SEC’s ties to Prometheum, suggesting possible special treatment. Prometheum’s ties to Ethereum and the SEC further sparked the infamous “ETH Free Pass” theory, meaning the Biden SEC (And Treasury) was likely paid off or made backroom deals with the Prometheum/ Ethereum people to circumvent regulations, while cracking down on the competition, such as Ripple and others. This explains the Ripple lawsuit. Xiao Feng and Vitalik are the most relevant figures in connection to both companies. Xiao Feng founded Wanxiang Blockchain, a seed funder of Prometheum. Vitalik is a “Chief Scientist” at Wanxiang. Wanxiang held several summits to host blockchain experts for panels to discuss the advancements of blockchain technology. One event included Vitalik Buterin, Founder of Ethereum and Chief Scientist of Wanxiang Blockchain Labs, Gavin Wood, Founder of Polkadot, Jed Mccaleb, Co-founder of Ripple and Stellar, Nick Szabo, Inventor of Smart Contract, Jae kwon, Founder of Cosmos and other blockchain influencers. A friend of Xiao Wang and Jed McCaleb is Lilin Sun. Sun was involved with McCaleb’s file sharing service ‘e-Donkey’. He was also present with McCaleb at Feng’s Wanxiang Blockchain summit mentioned earlier. Sun founded a company called Juzix and is CEO of another company called Juzhen Financials. Juzhen is funded by both Fenbushi Capital and Wanxiang Blockchain. None of these criminals are a Savage friend. They live in a forrest we need to burn down.
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19. The Octopus tentacles are deep here. This is the WELL where the deep state gets a ton of funding. A woman named Ada Xiao works (worked) at all the following at one point: Wanxiang Blockchain, Juzhen Financials, Juzix, and PlatON. PlatON, a Xiao Feng company, works closely with HashKey, another CCP-tied venture capital company. HashKey has investments in the following: Lightnet, a Southeast-Asia company JedMcCaleb is closely tied to with a long-standing partnership with Stellar and Velo Labs where he is an advisor. Prometheum, again founded and funded by Xiao Feng and Vitalik Buterin. Mask Network, a company with deep ties to Ripple. Deng Chao has been a longtime employee of HashKey, as well as being employed by Wanxiang Blockchain’s parent company Wanxiang Holding Co., Ltd at the time of the famous Blockchain summit with McCaleb, Vitalik, Xiao Feng and the others mentioned earlier which was at the very early years of their respective blockchain’s, Ripple/ Stellar, Ethereum, and Prometheus.
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20. Tron, HTX, BitTorrent, OpenGarden + Livio Weng, Group Chief Operating Officer of HashKey Group was the CEO of HTX (formerly Huobi), a company funded by CCP-tied ZhengFund. HTX was used by Tron founder Justin Sun to transfer large amounts of USDT (Tether) after significant withdrawals from other platforms. Sun also served as a Global Advisor for HTX. The same year Sun faced SEC charges for fraud, HTX suffered a “security breach” that resulted in a massive $258M “hack” under Sun’s watch, leading to suspicion that the funds stolen were an inside job directed at Justin Sun. A wallet (0x9ea1) was found to be linked to the missing funds account that went to Xiao Feng’s Wanxiang Blockchain. No shock to my Savages. Justin Sun’s Tron acquired a P2P file sharing company called BitTorrent. BitTorrent was a communication protocol for peer-to-peer file sharing (P2P), which enabled users to distribute data and electronic files over the Internet in a decentralized manner. The protocol was developed and maintained by Rainberry, Inc., and was first released in 2001 and co-founded by Bram Cohen and Ashwin Navin. Bram Cohen was often accused of being Satoshi Nakamoto as a front story. To his credit he denies it because anyone who looks into it knows it is impossible. While there he managed BitTorrent Labs, a research and development department of BitTorrent where he presided over a successful re-architecture of a new BitTorrent client: uTorrent Web. He left BitTorrent in August 2017 to found Chia Network. He has served as Chairman and CTO of the Chia Network since its founding as CEO.
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21. Epstein and the shitcoiners of the WEF and Silicon Valley are all linked. Other relevant people involved with BitTorrent are: Stanislav Shalunov, Ben Teitelbaum, and Greg Hazel. All three men have invested in and co-founded a company called OpenGarden. OpenGarden has funding from the Joichu Ito’s Digital Garage (former MIT Media Labs director before being pushed out for his close relationship and funding from Jeffrey Epstein). Digital Garage is also directly connected to Jeffrey Esptein as Epstein would use Ito as a proxy to invest in several crypto, AI and pharmaceutical companies. AI companies all have Epstein's and MOSSAD DNA in them and this is why I have told you to AVOID them all. Stanislav Shalunov of OpenGarden is a member of Lifeboat Foundation, alongside Jeffrey Epstein, Vitalik Buterin of Ethereum, and the many other crypto leaders mentioned in this thread. Stanislav Shalunov and Greg Hazel of OpenGarden and BitTorrent are founders of Fora Capital, a hedge fund firm that uses AI, machine learning and mathematics for trading in financial markets. This is how they will bleed you dry. Ben Teitelbaum of OpenGarden and BitTorrent went on to become VP of engineering at Blockstream, a company backed by many crypto juggernauts including Khosla Ventures, Bitfinex, Blockchain Capital (Brock Pierce/ Peter Thiel), Reid Hoffman of PayPal mafia who has his own long-standing relationship with Jeffrey Epstein, and Adam Back, the man who went back and forth emailing with Satoshi Nakamoto. Satoshi never revealed himself to Back for a good reason = MUNITIONS ACT and the Turing connection tied to the UK. Blocksteam is also funded by joichu Ito/ Jeffrey Epstein’s Digital Garage. Li Ka-Shing funds Blockstream through his Cheung Kong Holdings as well as the others just mentioned. Li Ka-Shing works with Horizon Ventures and the CCP-linked Cheung Kong Holdings, a subsidiary of CK Asset Holdings Limited. Be wary of your hero's folks. Some of them ain't who you think.
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22. How did this criminal cabal try to centralized mining to control Bitcoin? Here are the early players: Alibaba, Ant Group, Ripple + HashKey CEO, Dayong Zhang, is a former longtime GM of Ant Group, a CCP-tied conglomerate. Ant Group’s AntPool is responsible for a large amount of Bitcoin mining doing back over a decade. Ant Group has funding from several large CCP-tied firms, as well as Silver Lake, a firm where Brad Garlinhouse, CEO of Ripple, is an advisor for. Silver Lake helped fund Alibaba, a Chinese/ CCP tied conglomerate founded by Jack Ma. Alibaba also funded by AME Cloud Ventures (Chinese origins), a company co-founded by Jerry Yang. AME Cloud Ventures has funding in Ripple. Jerry Yang of AME Cloud Ventures is a member of the board of directors for Alibaba. Two other chinese men who work with AME Cloud Ventures, Jerry Chih Yuan Yang and Wretch Chien, are co-founder and former director (respectively) of Yahoo! Brad Garlinghouse of Ripple was SVP of Yahoo! for many years and at the time Jerry Chih Yuan Yang and Wretch Chien were at Yahoo! Alibaba is also funded by Eight Roads Ventures, a VC that funded Prosperity Marketplace, a company Ripple co-founder Chris Larsen was a co-founded and was president at during these same years. Another Alibaba funder, Tiger Global, is a funder of Ripple as well with their own ties to both China and Russia. Yuri Milner has ties to Tiger Global, as well as being a funder of Jared Kushner’s Cadre real estate company, with the help of George Soro’s firm, Soros Fund Management, which funded Ripple subsidiary (now defunct) Polysign where David Schwartz, CTO at Ripple was a board member. Jared Kushner’s good friend Ken Kurson sat on the board of directors at Ripple as well until just a few years ago. Yuri Milner, Jack Ma of Alibaba, and Pony Ma of Tencent (CCP-linked congolmerate) are all members of the “Breakthrough Prize”. Kushner real estate empire had to bailed out last minute by new Canadian Prime Minsiter and WEF support Carney. Never forget how the elites are linked via money. Breakthrough Prize honors important achievements in the categories of fundamental physics. It is sponsored by Sergey Brin and Anne Wojcicki, Mark Zuckerberg and Priscilla Chan, Yuri and Julia Milner, and Jack Ma and Cathy Zhang. All these people have direct ties to Chinese elite who have ties to the CCP and Chinese government, both directly and indirectly. Brin and Wojcicki are Bolsheviks at heart with deep ties to the One world fascist transhumanist agenda.
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1. Today's lesson: Your longevity experts are RETARDS. If you know you know. This is the lady below that shows you every longevity expert out there is FOS. She is and was the ultimate wellness rule breaker who lived 122 years and 164 days. Longer than anyone in recorded history.
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2. Her daily routine: ↳ Smoked 2 cigarettes daily until age 117 ↳ Ate 2 pounds of chocolate per week ↳ Drank Port wine regularly ↳ Doused everything from the Sea/land in animal fats and olive oil She also took up fencing at 85. Rode her bike until 100. Walked until she was 110. She only quit smoking because she went blind and could not see her cigarette to light it. She was the opposite of this rich moron below.
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3. The Decnetralized Science Behind It Her mitochondrial colony were exceptional. She sat out in her flower garden every day of her life. She was a young woman when the Eiffel Tower opened and was present. She was there for its 100th anniversary as a guest of the French government. Studies on her found she had mitochondrial epeigenetic variants that enhanced cellular photo repair and maintenance. She was the first human who showed us that environment trumped our nDNA and diet. But centralized science continues to miss this lesson and you pay that toll every day with their evidence based advice. None of you realize it. How can I say this? Did you know that recently a paper was published in Nature Medicine that was a massive analysis from the UK Biobank on this topic. Do you know what it revealed? It revealed the lesson Ms. Calment life; that our environment – the "exposome" of everything from air pollution to workplace light stress packs a bigger punch on how you age and die than your diet or DNA ever could. It tells us why all our longevity advice is horribly flawed.
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4. Ms. Calment befuddled the experts this caused researchers to study her life and they found what actually supported her longevity: ↳ Consistent movement adapted as she aged OUTSIDE ↳ Strong social connections via her network ↳ Positive outlook in life and humor in the face of defeat ↳ She ate a Mediterranean Sea based diet filled with DHA and used little to no technology in her life. People were her iPhone. Sounds like what I have been teaching all of you but all you do is argue with me for citations and BS questions. You were born to imbibe these basics. Begin!
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5. Your Job Could Be Shaving Years Off Your Life – And It's Not Just in Your Genes Why does this matter? Genetics might be your blueprint, but your environment is the architect rewriting the plans. Experts are buzzing: Forget chasing gene therapies, because real wins come from fixing what's around us. Cleaner air, better jobs, kicking bad habits? These could add years to your prime.This isn't just science; it's a wake-up call. Your cubicle, commute,your computer terminal, or corner store might be aging you faster than Father Time. Time to rethink: What in your world needs a upgrade? Time is you most valuable asset.
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6. Share if this hit home because we need to spread the word and live longer!Imagine this: You've got "good genes," but your daily grind, zip code, and bad LIGHT habits are secretly accelerating your biological clock faster than a ticking bomb. A groundbreaking study of nearly 500,000 people just dropped the mic on aging, and it's a game changer. Published in Nature Medicine, this massive analysis from the UK Biobank reveals that your environment – the "exposome" of everything from air pollution to workplace stress packs a bigger punch on how you age and die than your DNA ever could.
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7. The retarded longevity experts and functional gurus convince you biomakers and genes are the key. You read bullshit like this below and not one of them tell you that SUNLIGHT mitigates everyone one of them. https://t.co/iW5VkakeHm
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8. They also tell you glucose and insulin kill you but there cannot explain why animals who have the same noin visual opsins as humans use glucose as antifreeze to live in deep winter with a set of death genes in us to reserve time. These are the people HARMING your Time Bank Account.
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9. LIFE AND DEATH ARE DIURNALLY LEARNED BEHAVIORS OF COMPLEX LIFE. What are the human DEATH Genes Ms. Calment keep under wraps? Thanatotranscriptomic genes. Every hear of these genes that pay attention to your PRESENT ENVIRONMENT NOW? Redox Drain Impact: Draining redox power locally from the electronic state of cells would be expected to impair mitochondrial repair, thereby sustaining UPE-driven damage, which aligns with the post-mortem context of thanatotranscriptomic genes. Cells appear to have a need to drain themselves of light at death in a particular manner, and this mechanism explains why the light release Popp saw in sickness and when death happens. Prior to death, cells "empty" their light by exhausting their redox potential (NAD+/NADH, FAD/FADH₂), which powers electron excitation. As ATP production ceases and membranes depolarize, stored energy is released from the vibrational level in cells as UPEs, effectively draining the cell’s photonic "reservoir."
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10. Key bombshells from this paper: 25 environmental culprits identified: Things like socioeconomic status, sex life, LIGHT STRESS, and even where you live are directly tied to "proteomic aging" (fancy term for how your proteins break down over time) and higher mortality risk. This defines your ubiquitin marking. More marking less TIME. Poverty and tech abise steal your youth: Low income and location emerged as top villains, speeding up premature aging and death MORE than genetic factors. Environment trumps luck: While genes play a supporting role, modifiable exposures like pollution, social isolation, and poor sleep drive disease risks way harder. Why Uncle Jack has always laughed at the biochemists and food gurus......... Diet? Jury's out: The study couldn't nail down reliable diet data, because food really does not matter as much as many believe but environmental factors screamed "change me now!" for longer, healthier lives. I am still LOLing. CITE Integrating the environmental and genetic architectures of aging and mortality M. Austin Argentieri, Junhui Huang, Chirag M. Lakhani, Chirag J. Patel Nature Medicine, volume 31, pages 1016–1025 (2025) DOI: 10.1038/s41591-024-03483-9 Published online: 19 February 2025
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11. Just shut up and follow the SUN. That is Nature's Vitae. https://t.co/cf2BcKxQqn
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12. End of Lesson. https://t.co/bqlykAiPzf
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13. @threadreaderapp make me a roll.
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Two key things happen to a fluoescent when they near death. The flicker rate rises exponentially and cause stroboscopic effects and then when the fluorescent bulb nears the end of its life, the mercury vapor inside begins to condense at the colder ends of the tube or be absorbed by the phosphor and glass. The reduction in mercury vapor causes the argon gas inside the bulb to take over as the primary discharge medium. Since argon gas emits light at specific deep red and near-infrared (NIR) wavelengths when excited, the NIR emission from fluorescent bulbs increases as they age. The spectrum is still mostly in the blue light hazard range but a flash of NIR shows up for the first time in the spectroscope. This is how we know the bulb is dying. The best light for us shows up when the bulb dies and it is clouded in flicker which is also harmful to us. Interestingly, the IR-SENSE technology can identify aging bulbs before this light and flicker effect becomes visible to the eye causing dimming of the entire fluorescent tube fixture. Savages should NEVER use these bulbs unless they want to become ill and die sooner than they should.
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2. Compare the spectrum in the first tweet with this chart......you begin to see the problem of melanopsin dissociation from Vitamin A which frees it and it becomes a wrecking ball for all photo receptors, visual and non visual = MODERN DISEASE EPIDEMICS https://t.co/NB77eW51Zf
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3. And this is the mechanism of disease and death of the technocracy you all abuse. https://t.co/eEPtbzXQbk
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The bathypelagic and the sunless depths below house 85 percent of the ocean’s life, the largest living space on the planet. Your gut is also sunless and holds more cells than you do, so how does it handle light in its dark tube? Link to Photo-Bioelectric Thesis My thesis emphasizes light as a decentralized regulator of bioenergetics. In sunless zones, endogenous UPEs and microbial photobiology replace sunlight, maintaining hemiflusome and nanotube function. Disruptions (e.g., blue light from diet or nnEMF) increase entropy, impairing gut health (e.g., dysbiosis, autism links), correctable with red/NIR light and DDW. Bathypelagic Zone: Life in Sunless DepthsThe bathypelagic zone (1,000–4,000 meters below the ocean surface) is a sunless realm hosting ~85% of the ocean’s biomass, the largest living space on Earth. Despite the absence of sunlight, life thrives through unique adaptations: Bioluminescence: Organisms like anglerfish and lanternfish use bioluminescence, generated by luciferin-luciferase reactions, to produce low-level light (e.g., 400–500 nm). This light serves as communication, predation, and mate attraction, driven by chemical energy rather than sunlight (Widder, 2010, Science). Chemosynthesis: Bacteria near hydrothermal vents use chemical energy (e.g., hydrogen sulfide) to fix CO2, supporting food webs. This mirrors photosynthesis but relies on geothermal light output rather than solar photonic input. UPEs and Bioelectricity: Deep-sea organisms may exploit endogenous UPEs (e.g., from ROS in metabolic processes) as a subtle light source, aligning with my thesis’s focus on light as a bioelectric regulator. The Gut: A Sunless Internal EcosystemThe human gut, a dark tube with more microbial cells (10¹⁴) than human cells (10¹³), operates without direct sunlight yet maintains a complex ecosystem: Endogenous Light Sources: Gut cells and microbiota generate UPEs from metabolic activity (e.g., ROS from fermentation), measurable with photomultipliers (Van Wijk et al., 2008). These photons regulate cellular processes, akin to bioluminescence in the bathypelagic zone. Microbial Photobiology: Some gut bacteria (e.g., E. coli) express light-sensitive proteins (e.g., cryptochromes), responding to UPEs or ingested photoproducts (e.g., from diet). This suggests an internal photobioelectric network (Paulose et al., 2016, Microbiome). Melanin and Hemiflusomes: Gut epithelial cells contain melanin, which absorbs UPEs and ROS, protecting mitochondria. Hemiflusomes within these cells manage TCA cycle activity, exporting entropy as UPEs to maintain homeostasis, mirroring stellar entropy export. Handling Light in Darkness Both environments adapt to sunlessness by leveraging endogenous light and bioelectric mechanisms: UPE-Driven Bioelectricity: UPEs act as optical signals, guiding mitochondrial nanotubes and hemiflusomes to stabilize charge and oxygen levels, as seen in Liu et al. (2017). This prevents ER stress and supports immune function in the gut. Carbon’s Role: Carbon’s light-bending capacity (via melanin, porphyrins) enables these dark-adapted systems, reflecting its stellar origin as a threshold for life’s order. Entropy Management: Like stars, gut cells export entropy via UPEs, sustained by low-entropy food (e.g., DDW-rich diets), aligning with my entropy-export model.
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One politician can not make a government fraudulant. They need accomplices. Their supporters will say they were never elitists, but the research data I have pulled from my informants say otherwise. Grady Means was a card carrying member of the CFR for David Rockefeller. The data said that far too many children become the accomplices of cruel, indifferent men as fathers. They lie for these men. They lie to their own children. Because their fathers treated them exactly the same way. These kids always retain some hope that love is hiding behind the cruelty, so that the anguish doesn't drive them mad. Grady's book on "Felix the Flamingo" explains who he is and why these two are accomplicies to treason of the Fabians.
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What controls autophagy and apoptosis in mtDNA? Melatonin levels. This is why 95% of melatonin is made there. Now how did the system evolve from melatonin 600 million years ago? Meet the leptin melanocortin pathways. This was the basis of my Rubin Huberman pod 2 years ago. Most still have no linked the lessons I delivered back then. the leptin melanocortin pathways set the foundations of UPE and Quantum Signaling: UPE Origin: UPE arises from oxidative processes in mitochondria, where reactive oxygen species (ROS) like singlet oxygen or excited carbonyls emit photons upon returning to ground states. The energy of these photons (E = hc/λ) depends on the transition energy, typically spanning UV (100-400 nm) to near-infrared (600-1100 nm). Quantum Coherence: For internal signaling (e.g., mitochondria to DNA), photons must maintain phase and frequency coherence. This requires a resonant system, where emission and absorption wavelengths align, governed by quantum selection rules and environmental stability (e.g., avoiding decoherence from external noise). Melanin does just this. My Decentralized Thesis: Life evolves as a light-driven, electromagnetic system. Mitochondria and DNA act as antennas, with UPE encoding energy status between the center of a galaxy as it connects to a Galatctic sheet of plasma. Melanin absorbs all frequencies of light so it is optimized for this reception. Mitoception was born right around the time cephalpods came to be. As a RESULT melanin was brought to our interiors and became the motherboard of the cell. This stabilized endogenous UPEs and it created the 220 nm absorption spectra leptin has. Leptin became the ultimate light energy accountant and suplanted melatonin from its perch. This was a GOE event. See my @trikomes pod for more on that topic. Melatonin is a seasonal sensors, but leptin and melanin are way more sensitive for photonic and electromagnetic fields, not just chemical signals. Evolution made it the King. Melatonin was regulated to controlling the simpletons in life, the bacteria and Archea and this is what built mitochondria. That is why melatonin is mostly found there even today. 2. Post-Endosymbiosis Integration and Mitoception Challenge: After endosymbiosis (~1.5-2 Bya), mitochondria needed to communicate with the host cell. Successful integration required a sensory mechanism to monitor energy demand (burn rate) and oxidative phosphorylation (OxPhos) capacity (TCA/urea cycle stoichiometry) Mitoception Hypothesis: The brain evolved mitoception to “feel” mitochondrial status, likely via the TGF-β 1 superfamily cytokine family that includes inhibin and GDF15. This aligns with modern ideas of nociception, interoception, and immunoception, extending sensory networks to energy balance. Light as Mediator: Melanin’s ROS-scavenging and light-absorbing properties, amplified post-GOE (~2.4 Bya), suggest UPE as the original signaling mechanism. Rising oxygen tensions of the GOE enabled ROS-driven UPE, linking melanin and GDF15 to mitochondrial feedback. I am that dude. GDF15 Role: Induced by mitochondrial LIGHT stress of the GEO and the KT event (e.g., nnEMF, blue light, asteroids), GDF15 signals light energy imbalance via the brainstem’s area postrema (vagus). It correlates with ROS and UPE increases, reflecting OxPhos disruption. UPE Spectra: Stressed mitochondria shift UPE toward UV-blue (380-475 nm = blue light hazard) due to ROS (e.g., lipid peroxidation at 400-475 nm, protein oxidation at 340-380 nm). Healthy mitochondria emit more red/near-infrared (600-1100 nm) from efficient electron transport chain (ETC) activity. Melanin Link: Melanin amplifies UPE signaling via iron-chelating ROS generation under blue light, creating a quantum feedback loop. GDF15’s UPE release, tied to this mechanism, suggests a shared photonic mechanism for mitoception that is based on GOE, KT events and opsin evolution. Leptin and GOE Context Leptin’s Role: With a 220 nm absorption spectrum (UV), leptin’s signaling post-GOE aligns with oxygen-dependent UPE. This wavelength, absent in terrestrial sunlight, implies an endogenous light source, due to mitochondrial ROS emissions. Evolutionary Expansion: Over 600 million years, GDF15 and leptin integrated with the leptin-melanocortin pathway, enhancing neural complexity and consciousness via UPE-mediated mitoception. Game, Set, match food gurus.
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2. Decentralized Medciine#60 is now live here ----> https://www.patreon.com/posts/decentralized-60-129222655 How are meditation and consciousness linked in living things? Does the core of the galaxy link us in some way to the Galactic Electric plasma sheet that ties to every star we can see from Earth? How was that system built to work in you? Should it be done outside? Why?
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Why was Prague so hot this year for @BTCPrague ? The meeting was en fuego but something is cooking that may fry the technocracy's plans. The Mediterranean Sea is experiencing a thermal anomaly so extreme it’s being called a 1-in-216-billion-year event. To understand how rare that is: Earth is only 4.5 billion years old. This heat spike is 48x older than the planet itself. It’s 15x rarer than the entire age of the universe. And statistically, it’s as likely as winning the lottery 1,500 times in a row. So no — this isn’t “just a bad summer.” This is geophysical madness. And mainstream science has no explanation. They’ll blame CO₂. They’ll say “heat dome,” or “blocking pattern,” or “unusual atmospheric currents.” But ask them this: Why is the epicenter of ocean heating located in a tectonically active, magnetically unstable, semi-enclosed basin with active subduction zones and mantle volatility? They won’t answer — because they can’t. But CDIGR can. CDIGR (Core Displacement & Geodynamic Rebalancing) explains this perfectly: The Mediterranean Sea lies directly above the: – Hellenic Arc subduction zone – Calabrian Arc volcanic system – African-Eurasian compression boundary – Gibraltar Fault pressure node All of these are torque points in the planet’s crust — where energy from the inner Earth escapes. As Earth’s core slowly displaces, angular momentum and internal pressure rise, forcing heat upward through thin crustal zones. This upwelling mantle heat doesn’t just warm the sea — it’s altering ocean density, magnetism, and biological life. This isn’t from the sky. This is from deep within the planet. GRACE satellite data already shows mass redistribution under Europe and North Africa. Earth Orientation Parameters confirm polar wobble is increasing. The magnetic field is weakening over these same zones at a tremendous rate. SST anomalies are appearing exactly where CDIGR said they would: at trench systems, volcanic arcs, and mantle gateways. This is the Earth screaming through its crust. Mainstream science offers no mechanism , only centralized pseudoscience explanations tied to the observations. CDIGR offers a full model, with predictive accuracy and physical logic. This Mediterranean anomaly is not random. It’s not atmospheric. It’s the pressure valve of a rebalancing planet. You can believe in coincidence, or you can believe in pattern. I warned my Savages that the technocracy has some risks to its power and that Nature would respond. I told the EU the Mediterranean basis would become a flashpoint. And now it has. This isn’t climate change. This is a core event. Be ready Savages, Nature's answer to the digital euro, IoT, IoB, and all their nnEMF is incoming.
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2. Mainstream media has an agenda to gaslight Earth’s Magnetic Shield collapse and sell you the drama of climate change when it is not. This is how they are managing resources post event for their benefit. The weaker the magnetosphere, the more solar forcing pushes deeper into the mantle and core via the Global Electric Circuit. As a result, we get an acceleration in Earth’s energy imbalance and it leads to the pictures above. We’re now getting closer to the water boiling over on the stovetop = more lava and earthquakes where the mantle is rising. But what’s going on between the core and the mantle is more alarming if it reaches a threshold. What’s the most likely driver of how this is playing out? The poles are moving and weakening the magnetic shield due to a cyclical electromagnetic wave within this region of the galaxy called the Galactic Current Sheet. This is a more probable case because of the vast electromagnetic changes happening in our solar system and ALL of the planets now, not just Earth. People think the evidence is not in every other planet but it is. The Earth is not doing its own thing like it’s somehow its own closed off vacuum ignoring the solar system altogether. Earth, the sun and the planets are interconnected by this plasma sheet, just as our sun is and this is the stage that this play is being built upon. Many will be part of this coming experience, the next extraterrestrial Event won't be a 6 mile wide asteroid.
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3. When the magnetic field weakens on Earth we become a bigger target. If you are jabbed and we get hit with a small solar CME your chances of dying from a heart attack is higher than 3 X. FYI. https://t.co/H0e6Uvkavx
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4. When the thermohaline currents change the shit is about to get real. https://t.co/R19K2KuH8p
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5. When I was a resident I visited several physicists working on the Big projects for the US government in Livingston LA. When I told the DARPA physicist about the effects of transcranial magnetic stimulation on the human cortex, and how it worked in biology, he was stunned. I did this to illustrate why I believed what I now do about how the human brain functions. At this point, it would be wise for me to distinguishing regular “magnet therapy” from the effects of transcranial magnetic stimulation. The former magnetic therapy refers to the effects of a static, nonmoving magnetic field from permanent magnets. The latter refers to a magnetic therapy that generates a huge oscillating magnetic field, very close to your head, which induces electric currents in your brain. The movement of the Earth poles induces these currents. I explained to him you can not get a paramagnetic substance any closer to the neocortex then the location of blood vessels and CSF to the surface of the most active cells in the brain or heart. This maximized magnetic effects. When I was a neurosurgical resident, I visited a physics department where this quantum effect on the human brain was demonstrated to me, for my own amusement. They put a probe near my head and turned the current on and my arms twitched and moved from my shoulder to my fingers against my will. They were able to activate my neocortex with an oscillating magnetic field! They turned the magnet field over in polarity, and my arms twitched from fingers to my neck in the opposite direction showing how the DC direct semiconducting current Becker discovered in humans could be reversed when the field was reversed. This is when I realized why pole shifts could destroy living things with magnetic polarity changes. I then remembered reading accounts where Becker was able to use the same types of magnetic effects to induce complete general anesthesia in animals without ever having an emergency recovery from this type of anesthesia.
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6. Does the Earth’s Magnetic Field Generate the DC Current in CSF? The generation of the DC current is generated in a water layer right below the myelin layer in the CNS and PNS. This interfacial water is directly connected to what occurs at the interface between the neocortex and CSF in light and dark environments. Becker never figured this out, but I have been thinking about what he found for ten long years. I also had the advantage of being a neurosurgeon and operating a lot of brain’s and examining it in all its dimensions with my clinical observations. Any current created within the subdural and subarachnoid space also had to have an associated magnetic field with it, according to nature’s laws. This is why they are called electromagnetic field effects. Electric fields run at 90-degree angles to its associated magnetic field. It turns out this magnetic field has also now been found on the neocortex with the use of MEG and SQUID detectors in the last 20 years. The electric field was found in the 1930’ s by Hans Berger, who discovered the EEG waves of the brain on our skin. Becker was the first one to hypothesize the presence of a magnetic field in this situation because he was the first one to find that the DC current in humans came from the brain. He also knew all electric fields had to have an associated magnetic field because of Maxwell’s laws. He also knew from his experiments they had to use semiconduction to transmit a small current over long distances below myelin layer and above the axons in the CNS of all vertebrates. He proved biology used semiconduction because his experiments proved the presence of the Hall effect in bone and frozen nerves, which is only found in semiconducting circuits. Because he demonstrated this in the 1960’s, and his work was ignored, he indirectly showed me, why cold was primordial for humans and all life forms that use a DC current to generate energy. This effect has also been found in all plants and trees.
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7. DC Current in the CNS/PNS: Becker showed in experiment that a DC current exists in the interfacial water layer beneath the myelin, linked water chemistry to the neocortex-CSF interface, and they aremodulated by light and dark environments. This demonstrated that a DC electric field exists in biological systems, particularly in the nervous system of vertebrates, and is associated with semiconduction. Electromagnetic Fields (EMF): According to Maxwell’s laws, any electric current (like the DC current in the brain) must generate an associated magnetic field at a 90-degree angle. This is consistent with the detection of magnetic fields in the neocortex using modern tools like magnetoencephalography (MEG) and superconducting quantum interference devices (SQUIDs). Semiconduction and the Hall Effect: Becker’s experiments showed that biological tissues (e.g., bone, nerves) exhibit semiconduction, as evidenced by the Hall effect, which is a hallmark of charge movement in semiconductors under a magnetic field. This implies that the DC current in the nervous system operates in a way analogous to solid-state electronics, with implications for energy transmission over long distances. It also explains why CME can cause heart and brain failure acutely in humans. Earth’s Magnetic Field: While not explicitly mentioned as the source of the DC current in Becker's work, it has been shown over the last 30 years that the Earth’s magnetic field interact with biological electromagnetic systems, potentially influencing the currents or fields in the CNS/PNS/Heart. Diminishing Magnetic Field: the effects of a weakening Earth’s magnetic field, which is a known phenomenon, as the geomagnetic field has been decreasing in strength over time can easily impact life on Earth.
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8. Where we are today in science, in understanding how the brain really works, is close to where a man was 2,000 years ago in trying to understand how the planets moved in relation to the sun. We are nowhere close to where we should be. So if we are that far away in our understanding, how can we begin to make sense of it all? We can learn a lot from the macrocosm of space if we scale it to biology on this planet. My work does that for you, like you have never heard before. I showed you earlier in my blog series how molecular oxygen is delivered from the phytoplankton in the photic zone of the ocean to the ocean depths using the density of cold water to deliver it there. The more dense the water, the more oxygen is dissolved in it. The power of the sun’s photoelectric effect splits electrons from water in phytoplankton, which liberates oxygen. The liberated O2 becomes more dissolved in colder water by the laws of nature and chemistry, and then it is distributed all over the oceans by the thermohaline currents. Today, I am going to show you how the exact same process that happens on the surface of the earth is fractally designed on your own neocortex of your brain. It is happening right now in the ocean and this effect is huge for those who understand what it means. Normies will never get to this level. The very same process that works in the thermohaline current works in CSF that surrounds your brain and blood in your heart to bring higher oxygen levels to the surface of your brain using QED principles of the photoelectric effect, water chemistry and magnetism.
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9. My analogy above of the science happening on Earth is a progress report or report card and our current understanding of the brain being akin to ancient planetary models is a powerful reflection. It highlights the vast unknowns in centralized neuroscience, suggesting we’re still at an early stage of understanding how life responds to the cosmos. My proposal aims to draw parallels between macrocosmic processes (e.g., thermohaline circulation) and microcosmic biology (e.g., cerebrospinal fluid [CSF] dynamics) using fractal design and quantum electrodynamics (QED) principles and I believe it offers a novel framework to understand Nature better than we do.
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10. Thermohaline Currents and CSF Oxygen Delivery: In the oceans, phytoplankton use the sun’s photoelectric effect to split water, releasing oxygen that dissolves more in colder, denser water and is distributed via thermohaline currents. I'm suggesting a fractal analogy where the neocortex’s CSF system mirrors this, with sunlight (or light exposure) influencing oxygen delivery to the brain surface. The photoelectric effect in phytoplankton involves photons ejecting electrons from water molecules, producing oxygen. In the brain, I am implying a similar light-driven process might occur at the neocortex-CSF interface, possibly via QED (quantum-level electron interactions), enhancing oxygen dissolution in CSF.
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11. Density and Oxygen Distribution: Colder, denser ocean water carries more dissolved oxygen to depth. Similarly, I have proposed that denser CSF, influenced by water chemistry and magnetism, delivers higher oxygen levels to the neocortex. This density effect is modulated by temperature or ionic composition, aligning with physical laws governing solubility.
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12. Magnetic Influence: My earlier discussion of electromagnetic fields (e.g., Becker’s work, MEG detections) suggests magnetism plays a role in biological currents. In this model, the Earth’s magnetic field or the brain’s intrinsic magnetic field might guide oxygen-rich CSF distribution, akin to how geomagnetic forces interact with ocean currents. These have acutely changed now on Earth and nothing alive on Earth realizes it........
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13. Inflammation’s Role and CSF Density I've argued that inflammation reduces CSF density, altering biochemical processes. Inflammation likely increases temperature or introduces solutes (e.g., cytokines, ions), decreasing water density and thus oxygen-carrying capacity. This disrupts the fractal oxygen delivery system, impairing neocortical function. So a change in thermohaline currents mimics a huge acute magnetic change on your brain. Less dense CSF fails to support the photoelectric or magnetic effects needed for optimal electron or oxygen dynamics, potentially linking inflammation to neurodegenerative conditions or reduced neural efficiency. This leads to rapid disease generation by raising heteroplasmy. If it happens fast enough and at scale we call this an extinction event.
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14. My work in this thread shows you how having an innovative decentralized lens suggests that by studying nature’s large-scale patterns, we can hypothesize about the brain’s hidden mechanisms of how life operates.
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15. Given our limited understanding, my approach offers a starting point: Interdisciplinary Synthesis: Combine insights from oceanography (thermohaline currents), quantum physics (QED, photoelectric effect), and biology (semiconduction, CSF chemistry) to model the brain. This fractal scaling could reveal universal principles governing energy and oxygen flow across scales. Experimental Validation: Test the hypothesis with tools like MEG (for magnetic fields), EEG (for electric fields), or CSF analysis (for density and oxygen levels) under varying light and inflammation conditions. Becker’s semiconduction findings should guide experiments on charge movement in CSF. Macrocosm-Brain Analogies: We need to study how geomagnetic or solar influences affect ocean oxygen and extrapolate to brain responses using light therapy or magnetic stimulation to modulate CSF dynamics. Focus on Inflammation: Investigate how inflammatory markers alter CSF density and oxygen delivery, linking this to clinical observations from my neurosurgical experience.
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ALL CHRONIC DISEASES = lack of solar redox during daytime while having too much ALAN/nnEMF at day/night. Oh so you still think sunglasses, clothing, LED lighting, and sunscreen are good modern human ideas that don't affect the SCN or peripheral clocks in your cells? Consider nature's lessons carefully. What does full spectrum sunlight destroy naturally? UVA and B light naturally lowers adrenalin (the stress hormone of the sympathetic nervous system) while its photons re-zip collagen that cortisol release causes at 4AM that wakes us up by allowing water flows to occur between glial cells and neurons via the aquaporin 4 gates in the brain. AM sunrise light has no UVA or UVB present initially. It has blue, green, and red present. It has more blue than any other part of the spectrum and this is stimulatory to waking us up. Naturally, UVA light shows up later in the AM, depending upon your location in latitude, and this frequency of UVA light acts to begin to re-zip the collagen in our skin and eyes. That initial blue light stimulus from the sun’s rise is used to unwind our collagen to increase water flows to stretch the interspaces in neurons to wake our body and mind up at dawn from sleep. The aquaporin 4 gates are what are destroyed in Multiple sclerosis, which is another autoimmune condition. When we are missing UV and/or IR light for any reason, these photoelectric and photochemical are not made. When full spectrum sunlight is absent in someone who is chronically stressed for any reason, sleep cannot be induced by the adenosine chemical signal from the hypocretin neurons because the incident light signal of blue blocks it. What else blocks cellular regeneration by circadian de-coupling? Lack of full spectrum solar exposure is the most common reason and most overlooked issue in all of medicine these days. Proper ocular melatonin cycle requires that these two frequencies (UV/IR) of light be present to stimulate the regeneration processes in the eye during daytime. It also requires ABSENCE of blue 400-465nm at sunset!!!! When these things are off the result always = INFLAMMATION = too many protons and/or not enough electrons at the mitochondrial cellular level. If you think about your childhood, when you spent the day at the park of the beach, you might remember how easy it was to fall asleep and get a sunburn. The reason is simple, sunlight induces sleep because the regeneration pathways that use melanopsin need daylight to regenerate. When you did fall asleep, the redness of your skin did not come from the thermal burn, but it was from the increased blood flow due to the release of nitric oxide that acted to bring the arterioles of the dermis layers to the surface. This is a natural photochemical change induced by sunlight to allow the skin to absorb the UVA and UVB light at the surface. UVA and UVB light does not penetrate deep. To absorb the UV light we need the circulatory system to come from the dermis because UV light does not penetrate skin more than a millimeter. The NO engorges and vasodilates the arterioles containing the RBC’s. The RBC’s are filled with hemoglobin and porphyrins that absorb both UV and IR frequencies. Form meets function photoelectrically. The sunburn is really an absorption of too much thermal IR energy. It is a time phenomena not a sun phenomena based upon your sun callus and skin type. Deep sunburns can result from several factors: excessive sun, or thin skin, thick skin, or a poor adaptation to seasonal light due to chronic use of UV blocking makeup, clothing, or sunblock use in strong light cycles. Today we bury the sunlight and live under alien sun's at night and get diseases caused by inflammation. The sun is not the cause of our problems..........no matter the paradigm's belief or your own. Sunlight is a gift of Nature. UVB = Vitamin D UVB = Sex steroid off-switch UVB = Melanin production/fecundity/fertility UVB = β-Endorphins production UVB = Analgesic UVB = Leptin Sensitivity via adiponectin/placenta UVB = Weight-Loss/satiety/appetite regulation UVB = Anti-Viral/fungal & Anti-Bacterial/mold UVA = Nitric Oxide = Blood Pressure Regulation Controls stems depots for Acetyl choline neuron regeneration, weight loss IRA = Melatonin Production IRA = Photoprevention vs Sunburn IRA = Builds coherent water domains IRA = Anti-inflammatory lowers pain IRA = Builds Collagen/piezoelectric Red Light = Mitochondrial Function, H20, CO2 NO production Red Light = Reduces Blood Clotting Blue Light = Circadian Health (morning) Blue Light = Stimulates stem cell programming Blue Light = Adipose Regulation with IR-A and UV
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2. My thesis is life evolved decentralized systems governed by light, using UPEs, electromagnetic fields, and quantum-level processing is reinforced by the AD-light dysregulation connection. The ipRGC-SCN-habenula pathway, melanin’s photophysical roles, and SCAN’s concentric organization all reflect this principle, supported by the ECS. Modern light environments, ALAN, LEDs, sunglasses, disrupt this harmony, driving inflammation and diseases like AD, MS, and mental health disorders, but AM sunlight, full-spectrum light, and circadian alignment can restore balance, leveraging light’s primacy to enhance health. This decentralized perspective reveals life’s true essence around light, charge, and resonance, a truth the retina, brain, and mitochondria embody. CITES https://jlb.onlinelibrary.wiley.com/doi/full/10.1189/jlb.3RU1015-451R https://medicalxpress.com/news/2022-08-insights-retinal-neurons.html
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3. I reframe the GOE’s as an electrical crisis: life evolved decentralized systems to manage oxygen’s electromagnetic stress, using heme proteins, UPEs, and quantum-level processing, with light as the primary regulator. The Leptin Rx leverages this ancient wisdom, using sunlight to restore circadian alignment, support the ECS, and mitigate modern stressors like blue light, nnEMF, and ferroptosis, which drive diseases like AD, MS, ALS, and mental health disorders. This decentralized perspective reveals life’s true essence, light, charge, and resonance, a truth encoded in mitochondria, heme proteins, and the brain since the GOE.
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4. The Cost of Silence and the Toxin of Centralized Medicine: A Call for Common Sense New blog. Every word we utter carries consequences, but so does every silence we choose. Silence when you know better can speak louder than ignorance shouted from the rooftops. Yet, centralized medicine and its cadre of scientists seem deaf to this truth. For too long, the American taxpayer has been footing a trillion-dollar bill each year, following advice that yields no return on equity (ROE). Chronic diseases like demyleination are exploding, and the technocracy’s light, sold as progress, has become a toxin, poisoning our health and our future. I give you more answers to the puzzle today. https://www.patreon.com/posts/decentralized-48-128024635
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5. If you have a demyelinating disease like BPD, AD, PD, ALS, Depression, Schizophrenia, MS, and Autism pay attention. A meta analysis of 29 studies found that blue blockers can: → Improve sleep quality. → Help you fall asleep faster. → Reduce insomnia in shift workers, travellers & sleep disorders. → Advance your circadian rhythm (sleep earlier, wake more refreshed). → Even lower manic symptoms in bipolar disorder because of myelin improvements! Your eyes contain light sensitive cells that suppress melatonin, especially when exposed to blue light and some green (from phones, screens, lights). Blue-blocking glasses create “virtual darkness” → triggering melatonin release → telling your body it’s time to wind down. This prevents hormonal disruption, as blue light at night can raise cortisol, disrupt leptin signalling, and lead to insulin resistance. In simple terms increased hunger, and weight gain in the long run. Why they're an easy win: - One-time purchase. - Portable, effortless, and fits any lifestyle. - They're safe if used when your sensing blue light not in solar spectra Buy glasses that have been tested properly : http://www.luciaeyes.com Put them on after sunset, 2 hours before bed and use in tandem with circadian friendly lighting like candles You will likely fall asleep faster, sleep deeper, and wake up easier. Meyelination require optimal circadian signaling.
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6. Blue Light Toxicity and Systemic Effects: Chronic blue light exposure disrupts the ipRGC-SCN-habenula pathway, leading to flatlined cortisol cycles, suppressed dopamine and melatonin, and hyperactivation of glucocorticoid receptors (GRs) in the SCN, PHb, and hypothalamus. This suppresses adrenal cortisol secretion, a hallmark of blue light toxicity in modern humans. Exogenous steroids, when combined with blue light toxicity and low vitamin C, amplify this dysfunction, contributing to steroid-induced psychosis and mental illness. The literature also shows us nicotine addiction’s link to this pathway, that blue light-toxic individuals show reduced sensitivity to nicotine due to altered ACh receptor dynamics, while blue-blocking glasses may increase nicotine sensitivity by restoring balance.
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7. ipRGCs, Melanin, and UPEs: ipRGCs, like the retina’s broader metabolic strategy to use a Warburg metabolism where melanin is absent, are light-sensitive and vulnerable to blue light toxicity. Melanin, present in the retinal pigment epithelium (RPE) and potentially acting as a cryptochrome chromophore (Leask, 1992), amplifies UPE production through its broad-spectrum light absorption and radical generation. Blue light overstimulates melanopsin in ipRGCs and melanin in the RPE, increasing ROS and UPEs (380-450 nm), as predicted for GDF15-related mitochondrial stress. This disrupts dopamine and melatonin synthesis, impairing ipRGC regeneration and circadian signaling to the SCN and habenula. The resulting UPE spike signals mitochondrial stress, elevating GDF15 and contributing to disease, aligning with your thesis’ emphasis on light-driven quantum feedback loops which are recursive.
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8. Habenula, SCAN, and Neural Circuitry: The habenula’s role as a light relay center, connecting the retina to the midbrain and to the frontal lobes, complements SCAN’s concentric organization in the motor cortex. This is a recursive light loop that controls the entire physiology of the human. Both structures operate in a decentralized, non-hierarchical manner, integrating sensory (light via ipRGCs), cognitive (habenula’s role in mood), and motor signals (SCAN). Blue light-induced depletion of dopamine and GABA in the habenula disrupts this integration, impairing SCAN’s distributed processing and contributing to mood disorders and neurodegeneration. Melanin’s enhancement of action potentials and proton conductance (via its semiconductor properties) supports neural circuitry in both regions, but blue light and nnEMF disrupt this, slowing conduction and increasing UPEs, as seen in MS and ALS. nnEMF disrupt myelination at some level in all these diseases and this affects the neurologic function distal to the defect by altering UPE spectra.
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9. Tell me, you think food guru or health influencers can get you to this level? If so, let me know so I can block you from my feed.
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10. The internalization of melanin from primate to hominid gave us the ability to tap the absorption spectra of and the specialization of aromatic amino acids. This occured after 600 million years of the conservation of DHA in the CNS of compext life reflect the general rule of evolutionary complexity: expanding endogenous UPEs to process information at a quantum level. The movement of POMC to chromosome 2 in humans optimized this system, enhancing the brain’s ability to generate and respond to UV-range UPEs, driving the emergence of advanced consciousness. This built a recursive photonic loop between the sun and our cells that allowed for CNS complexity to explode in short evolutionary time scales giving silly talking monkey's abilities no one can explain until now. Decentralized Medicine has a path to explain this. https://bigthink.com/starts-with-a-bang/physics-consciousness/
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11. @threadreaderapp make me a roll.
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1. It is time to begin to Question the Status Quo: A New Track for Light and Life My dissatisfaction with the current use of light in modern life is a catalyst for breakthroughs. It is a fact that we’re blind to most of the electromagnetic spectrum, and this invites us to look where no one has looked before. What if we redesigned technology to mimic the sun’s full spectrum, reducing blue light dominance? What if we decentralized tech design, empowering communities to create devices that prioritize biological harmony over profit? This aligns withmy tribe’s ethos of integrity and character: a collective that challenges conventional thinking, seeks truth, and innovates for the greater good. Living under the sun’s visible spectrum does broaden the horizon of thought. Full-spectrum light enhances neuroplasticity and mood via serotonin pathways (Journal of Neuroscience, 2019), while reducing the oxidative stress caused by blue light. It’s a return to a decentralized, natural system, much like I teach my tribe daily, which operates free from artificial interference. By keeping your interests broad and refusing to let your mind be stunted, you’re embodying the ancient photonic lesson: don’t accept the limited window of reality you’re given. Question, explore, and innovate. We will explore this today with @SabinehazanMD and @dralexisjazmyn
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2. n the 21st century, the dissemination of healthcare knowledge has been hijacked by influencers and grifters, sidelining those who champion first principles thinking. Drawing on Ayn Rand’s 1960 essay, Faith and Force:OREM The Destroyers of the Modern World, we can identify the deeper philosophical corruption behind this shift: the triumph of mysticism over reason. Rand’s argument, that cycles of prosperity and destruction stem from the conflict between reason and mysticism, offers a lens to understand why superficial, emotionally charged narratives peddled by influencers often overshadow rigorous, evidence-based discourse in decentralized healthcare.
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3. Rand posits that reason is the only objective means of communication, grounding human understanding in reality. In contrast, mysticism claims to knowledge beyond evidence or logic breeds confusion and manipulation. Historically, she attributes periods of stagnation, like the Middle Ages, to mysticism’s dominance, while the Renaissance’s rediscovery of reason fueled capitalism’s prosperity. Today, the healthcare information space mirrors this dichotomy. First principles thinkers, those who deconstruct complex problems to their fundamental truths and build solutions from scratch, rely on reason drawn from the fundamental laws of nature. They advocate for decentralized based medicine, critical analysis, and transparent methodologies. Yet, their voices are drowned out by influencers and grifters who exploit mysticism’s allure, peddling quick fixes, miracle cures, and emotionally charged anecdotes that resonate with a public craving certainty.
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4. The rise of social media has amplified this trend. Platforms like X, IG, and Facebook reward attention-grabbing content over nuanced arguments. Influencers, often lacking expertise, leverage charisma and storytelling to build followings, promoting unverified supplements or debunked therapies. Grifters, more cynically, exploit vulnerabilities like fear of illness, distrust in institutions for profit. Both thrive on what Rand calls “supernatural means of knowledge,” bypassing evidence for claims that feel true because they are emotionally compelling. For example, wellness gurus touting detox diets or supplement conspiracies gain traction not through data but through narratives that promise empowerment or secret knowledge. Meanwhile, scientists and clinicians, bound by reason’s rigor, struggle to distill complex truths into viral soundbites.
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5. This is not merely a communication failure but a philosophical one. Mysticism, as Rand warns, makes persuasion impossible because it rejects reality as the standard. When influencers claim intuitive or anecdotal authority, they evade scrutiny, leaving no common ground for debate. First principles thinkers, by contrast, invite it, but their insistence on evidence and logic alienates audiences conditioned for instant gratification. The healthcare space, where lives are at stake, suffers most from this shift. Misinformation spreads unchecked from the cesspool network of influencers eroding trust in legitimate expertise and delaying effective treatments.
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6. The consequences echo Rand’s cycles of destruction. Just as collectivism stifled progress in the twentieth century, the mysticism of influencer-driven healthcare undermines the potential for rational, innovative solutions. To reclaim the pantheon of information dissemination, first principles thinkers must adapt, not by abandoning reason, but by mastering the art of translating it into compelling narratives. They must meet the public where they are, on platforms with clear, relatable messages that expose grift and restore reality as the standard. Only then can reason prevail over the modern mysticism of the influencer age. Soon on my website I will have a list of people who I information share with. I will also allow the public to to ask me about people they currently rely on on whether I would trust them to deliver decentralized advice based on their character and integrity. It is time to put all influencers under the disinfectant of sunlight. The public deserves to know who really is putting in the proof of work to help return "time equity" back to the public.
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7. WHAT MAHA MEANS TO ME MAHA weaves together the themes of authenticity, transparency, and the biological influence of natural light, building on our ongoing discussion about decentralization, the electromagnetic spectrum, and the integrity of your tribe. Distillation of the mantra: what is transformative power of transparency and the role of natural light in fostering genuine connections. I am focusing in a specific target for my tribe.
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8. The right people ask you questions; the wrong people question you. Embrace transparency. Transparency brings vulnerability. Transparency allows people to see us for who we are. The sun builds this transparency in our neural networks. When one projects a persona or wears a façade, he or she is only projecting a "virtual reality." This facade is built with manufactured light. This appearance is short-lived & will eventually fade, revealing the true person years later. Do you have time to waste? Time to burn to wait on them? We should share our confusion and problems rapidly to overcome them and make a connection or facilitate a disconnection. When we hide them from each other using the social media middleman, we effectively teach ourselves to hide them from ourselves. We normalize an unauthenticity. Share your concerns and interests with people because it builds your transparency. Then we can connect, and all grow together. The invisible threads built by natural light are the strongest ties we'll ever make. Consider making your mind an open book to others, or maybe just "think" as a photo album radiates." I have found out that many influencers have told people they are trying to swindle have told them they have a direct line to me. Only one person has a direct line to me. That is my nurse. If you did not hear it from me or her then you should consider it PROPAGNADA.
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10. Transparency is the antidote to propaganda. It’s the willingness to be vulnerable, to let others see you as you are, your flaws, confusion, and all. This aligns with the integrity and character: a tribe built on transparency operates with quantum coherence, each member’s authenticity resonating with the collective. By contrast, a facade, built with the “manufactured light” of screens and social media, creates decoherence, a fragmented, inauthentic state that disconnects us from ourselves and others. This is the canvas that influencer look to use and dominate.
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11. My metaphor of the sun building transparency in our neural networks maybe considered both poetic and scientifically grounded. The sun’s full-spectrum light, unlike the narrow blue light of screens, supports neural health and emotional clarity. Full-spectrum light enhances serotonin production, which regulates mood and social behavior (Journal of Neuroscience, 2019), and supports neuroplasticity by optimizing mitochondrial function (Photobiomodulation, Photomedicine, and Laser Surgery, 2021). This biological transparency where our neural networks function in harmony with natural rhythms mirrors the social transparency I advocate for. When we’re bathed in natural light, we’re more likely to feel grounded, authentic, and open, as opposed to the hyperstimulated, performative state induced by blue light, which suppresses melatonin and disrupts emotional regulation (Chronobiology International, 2022).
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12. Manufactured light fuels the virtual reality of facades. Blue light’s dominance in screens not only disrupts our biology (e.g., oxidative stress in heme proteins, as we discussed) but also shapes our behavior, encouraging curated personas over authenticity. Social media, a middleman built on this light, normalizes inauthenticity by rewarding facades, filters, edits, and highlight reels, while punishing vulnerability. This facade allows humans to hide our confusion and problems from each other teaches us to hide them from ourselves, creating a feedback loop of disconnection. This is the centralized system at work: it thrives on artificial light and artificial connections, keeping us from the “invisible threads” of genuine relationships. I am to change this process in my tribe beginning today.
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14. Hiding behind social media, as you point out, delays this process. It wastes time, it wastes your time, and can you afford to burn this TIME? The facade may hold for years, but it will fade, revealing the true person beneath. By then, the opportunity for real connection may be lost with any tribe. Transparency, on the other hand, accelerates the process, building stronger ties through what I like to call the “invisible threads,” are the bonds forged by natural light and authentic interaction. Employ via negativa everyday. Subtract the superfluous to get to the extraordinary. Your tribe, the light bringers, the game shakers, must be anchored in integrity and character, or they’re no tribe at all. It it time to stop complying with influencers if you wish to add time back to bank acoount. CITES https://www.instagram.com/p/DJVo4OlORQp/
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Check out my latest article: THE SILENCE IS US: Unlocking the Decentralization to Hear the Cosmos https://linkedin.com/pulse/silence-us-unlocking-decentralization-hear-cosmos-jack-kruse-9xuhe In 2025, humanity stands at a crossroads, grappling with impossible questions, like monetary collapse, cosmic isolation, and the limits of our own minds that demand more than logic alone can offer. Embracing the suck of the problem can expose the raw, messy struggle of failure and uncertainty. By doing so it unleashes our divine gift of creativity, a force that thrives in chaos and forges unexpected bridges between despair and revelation. It’s through this gritty, unpolished process that we tap into the sacred spark within, transforming the unbearable into the extraordinary and finding answers where none seemed possible.
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2. The path to meaningful change, as echoed in my words, demands resilience, action, and unwavering belief in your mission: "Never stop just because you feel defeated. The journey to the other side is attainable only after great suffering and you realizing you have to change your game plan when it FAILS you." For a clinician or a scientist becoming a champion for humanity’s bioelectric health, this means that ideation without execution leads to the deletion of even the best ideas. These concepts of mitigating nnEMF or blue light exposure remain useless without real action that moves the needle. As I've said countless times, "If you go ALL in I will not let you fall. I will catch you, drag you to the finish line," emphasizing that true progress comes from adapting on the fly, because "sometimes not getting what you want is a wonderful stroke of luck."
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3. But to truly succeed, you must heed this truth: if you do not believe in what you are doing, you'll never visit that which is extraordinary, you must change that about you now. Your best is out there waiting to be tapped, and your new network of silly talking mitochondriacs is ready to touch you overtly and covertly, pushing the world to a tipping point of bioelectric and ecological harmony. By taking concrete steps happens by executing research, advocating for change, and empowering communities; the clinician/scientist can ensure their ideas don’t fade into oblivion, aligning with nature’s rule: "When things go wrong, do not go wrong with them," but instead act decisively with belief to climb their "Stairway to Heaven" and create a lasting, extraordinary impact. Do not fade to black. The world needs you to be extraordinary when they are all Warburg shifted.
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4. An interview I recently did, is going to published and someone sent the first draft to me to review. “I put up with many years of you putting us down and watching us bleed, now I'd like to see you bleed some back." It is time to bleed the freak. https://www.youtube.com/watch?v=-xQQzi0IdLY&list=RD-xQQzi0IdLY&start_radio=1 "Dr. Jack Kruse Unleashes Truth Bombs: Time for the Establishment to Bleed Back “I put up with many years of you putting us down and watching us bleed, now I’d like to see you bleed some back.” That’s the raw sentiment echoing through Dr. Jack Kruse’s latest salvo against the medical world, delivered in a no-holds-barred interview with Andrew Huberman, captured by The Energy Blueprint on YouTube. Titled "Dr. Jack Kruse Drops KNOWLEDGE BOMBS on Andrew Huberman!", this 48-minute deep dive isn’t just a conversation; it’s a reckoning. Kruse, the neurosurgeon turned decentralized health revolutionary, takes aim at a system he says has failed us, armed with peer-reviewed science and a personal saga that’s pure defiance. Fresh off being booted from a Carnival cruise ship, a story that hit national news in 2012, he’s here to settle scores and rewrite the rules.
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5. Light: The Weapon We’ve Lost Kruse doesn’t mince words: modern medicine’s got it wrong, and light is the fix. “Your light environment controls your biology,” he told Huberman in 2023, hammering home how sunlight, UV and infrared especially, runs the show. It’s not woo-woo; it’s physics and biochemistry, backed by studies in journals like Mitochondrion and Journal of Photochemistry and Photobiology. Sunlight juiced up our mitochondria over eons, he says, those cellular engines that churn out energy and keep us alive. Today, we’re starving them with indoor lives and blue-lit screens, and the result? Exploding rates of disease like diabetes, neurodegeneration, you name it. He’s got data to back him up: UV light boosts nitric oxide, infrared repairs DNA, and morning sun syncs circadian rhythms. “The sun’s not your enemy,” he growls, flipping the sunscreen and sunglasses narrative on its head. For years, he watched patients suffer under a system that ignored this, and now he’s done taking it lying down.
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6. The Cruise Ship Standoff Kruse’s fight isn’t just academic, it’s personal. In 2012, he was famously ejected from a Carnival cruise ship, a clash that lit up news screens nationwide. The video doesn’t spill the details, but the timing’s no coincidence. Was it his outspokenness? A showdown over his principles? Whatever sparked it, Kruse emerged unbowed, channeling that fire into this interview. “They’ve put us down, watched us bleed,” he seems to say through every jab at the establishment. Now, he’s swinging back, and he’s got decentralized science as his fists. Calling Out the Gatekeepers Kruse doesn’t just critique, he accuses the Ivory Towers of crimes against humanity. He says "savages" have a RICO case against the centralized system. Medicine’s been hijacked by government/DoD, he claims, by drug-pushers and dogma that can’t handle the truth about light and magnetism. “They don’t understand how humans work,” he snaps, and Huberman, ever the centralized scientist, probes but can’t blunt Kruse’s edge. This isn’t theory; it’s battle-tested by the laws of physics. Studies show artificial light disrupts melatonin and metabolism, Kruse says it’s why we’re fat, sick, and tired. He’s not asking for a seat at the table; he’s flipping it over.
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7. The Payback Moment This quote fits Kruse like a glove. After years of seeing patients “bleed” under a broken system, and taking his own hits, from professional backlash to that cruise ship drama, he’s ready to make the gatekeepers pay. “Get outside, reclaim the sun while grounding,” he urges. It’s not just advice; it’s a war cry for his savages. The peer-reviewed lit backs him up: sunlight’s benefits aren’t fringe, they’re foundational. If the establishment’s been bleeding us dry with half-truths, Kruse wants their reckoning.
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8. Why This Matters At nearly 49 minutes, this isn’t a casual watch; it’s a manifesto of Nature's recipes in you. Kruse blends neurosurgical cred with a street-fighter’s grit, and it’s photo-electric. He’s not here to play nice or beg for approval. He’s here because he’s seen the damage, lived the pushback, and knows the science cold. The Carnival cruise ship incident? Just fuel on his fire. For anyone who’s felt crushed by a system that doesn’t listen, Kruse is the voice saying, “Enough, now it’s your turn to bleed.” Our Takeaway Dr. Jack Kruse isn’t dropping knowledge bombs; he’s detonating them. This interview is a middle finger to a medical world that’s failed us, a call to harness light like our ancestors did, and a promise that the fight’s not over. “I’d like to see you bleed some back,” he might as well shout, and with every study he cites, he draws blood. Watch it, soak it in, then step into the sun. His shot is being heard around the world. The decentralized revolution’s started, and it is time for savages to pick a side.
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9. Decentralization > centralization https://t.co/LchNpJopa1
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10. We can change people with our ideas. A mediocre idea that generates enthusiasm will go further than a great idea that inspires no one. There is one thing stronger than all the armies in the world, and that is an idea whose time has come. Do not rise to the level of your goals. Rise to the level of a decentralized system of thinking. This is where future success will be found. Why do we choose to believe some things and not others? Most of us think of ourselves as rational agents who can make decisions and form beliefs that make sense. But the world is far too big and complex for us to have the time or attentional bandwidth to know about everything, so we have to pick and choose. The scientific name for this is “sampling,” It works well in a dynamic world where the approximate truth is usually good enough to make everyday decisions. We’re also built to favor investigating the things we feel uncertain about. This tendency pushes us to expand and update our knowledge base. Once we feel like we know everything, we disengage and move on to the next thing. This prevents us from wasting time on what we already know so we can learn something new. The problem arises when we believe that we know everything there is to know, but we are wrong. This is the Dunning-Kruger effect. It also forms our own cognitive biases. When this happens, we are less open to changing our minds based on new information because we don’t seek out new information and are more inclined to ignore it when we encounter it. Try to build your circle of six with people whose minds operate like a parachute. When they jump into something new their mind is open. END OF LESSON
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TODAY'S LESSON ON SUNGLASSES. UV LIGHT, POMC, and HOW THEY ALL LINK TOGETHER. Ciliary ganglion controls how much light gets into the pupil and it controls the lens ability to refract and target light on certain parts of the retina. This is why a ciliary ganglionectomy has massive effects on melanin production in humans. Wearing sunglasses is a temporary way to give yourself a ciliary ganglionectomy. This is why sunglasses wearing leads to more sunburns. The ciliary ganglion contains postganglionic parasympathetic neurons that supply the ciliary muscle and the pupillary sphincter muscle. Because of the much larger size of the ciliary muscle, 95% of the neurons in the ciliary ganglion innervate it compared to the pupillary sphincter. Below see the detailed view of nerves of lateral orbit showing the ciliary ganglion immediately behind the globe of the eye.
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2. Decentralized medicine has a lot to say about how our tissues deal with light and water. The ciliary ganglion is a bundle of nerves, parasympathetic ganglion located just behind the eye in the posterior orbit. It is 1–2 mm in diameter and in humans contains approximately 2,500 neurons. The ganglion contains postganglionic parasympathetic neurons. These neurons supply the pupillary sphincter muscle, which constricts the pupil, and the ciliary muscle which contracts to make the lens more convex. This changes the target of light on the retina and this implies differerent tracts which begin in the retina are targeted based upon the light you chose to live under. Both of these muscles are involuntary since they are controlled by the parasympathetic division of the autonomic nervous system.
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The ciliary ganglion is one of four parasympathetic ganglia of the head. The others are the submandibular ganglion, pterygopalatine ganglion, and otic ganglion. Three types of axons enter the ciliary ganglion but only the preganglionic parasympathetic axons synapse there. The entering axons are arranged into three roots which join enter the posterior surface of the ganglion: 1. The sensory root branches from the nasociliary nerve and travels through the ganglion forming part of the short ciliary nerves. These sensory axons supply the cornea, ciliary body and iris. 2. The sympathetic root originates from the internal carotid plexus with cell bodies in the superior cervical ganglion. I'll have a lot to say on this nerve below in the thread. These axons pass through the ganglion and enter the eye without synapsing into the short ciliary nerves. The sympathetic root contains the postganglionic sympathetic axons that provide sympathetic supply to the blood vessels of the eye that come from the internal carotid artery loaded with melanopsin chromophores. Sometimes, they also supply the pupillary dilator muscle, however these axons usually travel from the nasociliary nerve to the long ciliary nerves to enter the eye. 3. The parasympathetic root branches from the inferior division of the oculomotor nerve and carries the preganglionic parasympathetic axons from the Edinger-Westphal nucleus to the ciliary ganglion. Within the ganglion the axons synapse onto the postganglionic parasympathetic neurons. These neurons project axons through the short ciliary nerves to innervate the ciliary muscle and pupillary sphincter muscle. Most centralized people do not truly understand what they eye really does for the decentralized organization of the human brain. Let's examine the implications.
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4. Why does chronic or short term damage to the ciliary ganglia cause problems related to tanning and solar charge connection? They eye not only sees the light, it refracts it and targets the retinohypothalamic tract that is begins in the inferior nasal part of the retina. Early morning sunlight hits this target as the sun rises higher in the sky. Early in the morning in most places UV light i snot present. UV-A and IR- A show up first and this stimulated the production of nitric oxide in the eye and in the head and neck of humans. This step is important in human melanation. These are DECENTRALIZED things your dermatologist does not even know, but is published in the literature, but your decentralized neurosurgeon does know and teaches you. Be careful who packs your parachute. @JuicefBukele https://pubmed.ncbi.nlm.nih.gov/12535208/
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5. See AM sunlight is the first step in Human melanin renovation. Ultraviolet B irradiation of the eye begins later in the AM and this light energy is transmitted in a nitric oxide-dependent manner through the ciliary ganglia involving the first branch of the trigeminal nerve to the hypothalamopituitary proopiomelanocortin system. If you do not get the upregulation of NO from AM light loaded with UV-A and IR-A light, UVB light becomes less useful to you and in some haplotypes can harm you. Yes, you paleo humans I am speaking to you. The disruption of this set of decentralized circumstances has huge implications. It results in diurnal upregulation of alpha-melanocyte-stimulating hormone secretion every day in controlled fashion and consequent stimulation of melanocytes in the skin. This is really why sunglasses are killers. It also implies why sunscreen is a centralized idea of the profiteers.
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6. Now about that superior cervical ganglion and how it links to the blue light non visual photoreceptor, melanopsin..........
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7. What connects your inner light creation to your filaments in cells? Is your life electric because your mitochondria in cells make a plasma called water? You do know that your mitochondrial also creates light via metabolism huh? Have you read the book below that shares that data? I know your dermatologist has not read it.
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8. Is your filament, called your gut, connected properly to your brain by sunlight and water? Are your brain and gut set up via coherent coupling of cycles between food and light of the day in your retina and brain? You do know food is an electromagnetic bar code of photosynethesis right? The vagus nerve does maintain this "watery connection" between the brain and gut over a water electric network. These two systems are CIRCADIAN harmonic oscillators that need to be properly coupled to work together. Do your centralized experts know this? What connects these two oscillators in our body? Water networks connect them both organs. Why do not centralized experts realize these connections exist in all of us?
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9. Sunlight makes the water in our cells a liquid crystalline PLASMA. It increases the amount of electrons in it. Water without deuterium has a high dielectric constant. DDW in the mitochondria is at 160. Water from your tap has a dielectric constant of 78. That means tap water with 150-155 ppm of deuterium in it does not have as many electrons as mitochondrial water and without those electrons sunlight cannot be be absorbed as well. This makes water made in you a BETTER electromagnetic capacitor = BATTERY. That is the battery all cell run on. Your brain has more mitochondria so it makes the water it needs to operate with the sun.......now do you get enough sun to run your epigenetic programs?
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10. That water cells need must be created by our colonies of mitochondria and this is how eukaryotes to bring the sea onto a land-based existence. Liquid crystalline = coherent water = a sea of electrons for redox chemistry to exist. Liquid crystalline water possesses long-range orientational order by pointing all the molecules by pointing in the same direction. This is an electric or magnetic polarization effect. It also allows for a translational order that allows them to keep their position as they move = topology effect. Liquid crystals are mobile and flexible and highly responsive to electromagnetic radiation in our environment. This allows them to undergo rapid changes in orientation or phase transitions when energy is added or subtracted from the water. This is why cell water responds vigorously to exogenous electric or magnetic fields.
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11. It is why water responds vigorously to temperature, pressure, pH, hydration, and concentrations of inorganic ions like phosphorus. I think the Universe is powered by water electricity and I believe every cell is powered in the same way. CSF comes from the water in blood plasma and then its chemistry is changed by the choroid plexus of the brain by iodine and salt. Salt levels control the physics of the coherent domains of CSF. In my opinion, It is the single most key mechanism in the brain from a quantum perspective. It changes the redox potential of the entire organ. Water is the energy that life runs on. Water is the universal electron and proton donor. When you understand these concepts, you begin to see that proton and electron currents in water made by sunlight create currents inside of cells and over extracellular distances that are capable of delivering physical and chemical messages concerning the redox status of all parts of the cell.
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12. I met two guys in August named Dave & Mike recently who did not believe that what is posted in the above slide in yellow was true. This means they do not understand decentralized networks or decentralized medicine. https://www.youtube.com/watch?v=_Inspd0gKEs&t=5s
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13. Water networks communicate this information by way of the vagus nerve. The water in blood plasma is a non-homogenous mix of water that has low UV absorption rate that can be changed as its dielectric constant changes with the addition of salt, anions, and iodine. Once the water in blood plasma becomes partially structured, this fraction of cellular water has better UV light assimilation as its viscosity and refraction are altered. Just adding a bit of salt to this water does this. Your body does this and so does a coconut. This is a clue for those who still remain vitamin D3 deficient despite getting "adequate" sunlight and/or use tanning beds that some other process in them remains lacking. If you do not believe it, you need to read some more. I know your centralized experts aren't on your behalf.
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14. Water is redox in humans. Water molecules are more than just made up of hydrogen and oxygen ions. These ions have electric charges and form dipoles. Water is not inert, its ions are dynamic, always rotating and vibrating. Due to the various bonds and kinks that form among water molecules, clusters of water can emit a multitude of electromagnetic frequencies depending on the number of water molecules and their bonds in the clusters. With different structures of water clusters, different electromagnetic frequencies are produced. This means that water can resonate at any virtually any frequency. How does it do this? Water must first absorb ambient electromagnetic radiation to re-emit it. Sunlight can activate oxygen’s outer electrons to higher energy levels and in 0.0000001 seconds, returns to ground level, emitting photons with a frequency of about 1,000,000,000,000,000 Hertz. Water is, in fact, a repository for electromagnetic radiation of all types. The human optical windows, however, operate precisely between 250nm-780nm. Proteins can utilize 200nm -900nm light. Water consists almost entirely of a type of elementary particle called a photon (a photon is a boson and bosons are the glue that holds matter together) and only a very small amount of water is actual matter and it is hypothesized that water is 974,600,000,000 parts photons to 1 part matter (hydrogen and oxygen). Water is mostly photons and photons are the force carrier (messengers of information) of the electromagnetic field. This explains how electromagnetic information is propagated at the molecular level, via water.
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15. All biomolecules are dependent on water. We are made up mostly of water, specifically structured, liquid crystalline water, which is imbued with a multitude of electromagnetic frequencies. We are always immersed in a plethora of natural and unnatural electromagnetic radiation in our environments, some beneficial, others harmful and it is constantly changing the liquid crystalline water in our bodies faster than we can think. The ambient electromagnetic environment is literally changing the way living water behaves in our bodies to create health or to fuel disease. This has tremendous implications for biology and medicine.This sets in motion the requisite core of chemical reactions that restore the local and global energy balance of all living things. The vagus nerve is our electric filament, the spark of life, found between seas of water in us. It is that nerve that connects two organs photoelectrically using water as its plasma to make free electrons/protons. Water is present on either end of this nerve. You must become a water muse, first and foremost. The vagus nerve controls the parasympathetic portion of the autonomic nervous system as the picture below shows. It begins in the area postrema of the 4th ventricle. The vagus is part of the parasympathetic system that lowers the stress response. Its activity drops chronically when the sympathetic system is constantly turned on. Your vagus nerve, ciliary ganglion and the superior cervical ganglion all connect via water networks in your brain and none of your centralized specialists know it. Uncle Jack decentralized courses he teaches do.
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16. The sympathetic system outflow of the stress stimulus begins in the paraventricular nucleus (PVN). The vagus nerve is the calming portion of the ANS and antagonizes the PVN to lower stress and INFLAMMATION. The vagus nerve is also key in allowing mitochondria to oscillate at 100 Hz to fat burn. Balancing both arms is critical in avoiding diseases, and creating allostasis. Autonomic nervous system (ANS) regulation is a function of light and water properly activating one another to control magnetic flux in the spinning ATPase on the 5th cytochrome. The vagus nerve connects dissimilar "bodies of water" within the human body to make them work coherently. They use the light in that environment to make a connection or allow a mitochondrial disconnection which disrupts energy flows. The stimulus of light on our skin and retina changes the water domains in CSF in the brain and in the gut. 99.8% of CSF is made up of cell water. This is how the “central digital” circadian system from the RPE of the eye, the skin, and gut are linked to the SCN which sits in a cistern of CSF above your optic nerves in your skull. Light waves are transformed to phonon vibrations in the water. When this occurs water becomes coherent and becomes a sea of electrons to run redox pathways in biochemistry properly and coherently. This allows all mitochondria to vibrate as one. The “analog circadian system” of the gut is linked to solar light exposure from food electrons and to the timing of food grown in the environment that cells get in our mitochondria so that the signals can be yoked via the area postrema (AP) and the median eminence (ME) in the brain. These two areas in the brain have no blood-brain barrier. They allow water and light communication to occur, so the electron density in the CSF is accurately tied to the local environment these neurons can sense. Electron density and coolness are linked in water. This is true in the ocean and in our cells and CSF cavities. For example, when we eat, 60% of blood flow is shunted from the peripheral blood to the gut’s mesenteric system by the autonomic nervous system. The brain senses and pays attention to these shifts, using the vagus nerve, as its main information highway. When the sun hits our skin (UVA and IRA light), nitric acid (NO) is released and 40-60% of blood flow raises to the skin surface to become radiated by solar radiation. This energy transfer is sensed by the vagus nerve in our superior cervical ganglion and sent to the brain to lower our stress response in the PVN. This stimulates melatonin cycles to work properly. So if your lifestyle buries the sun, you create a stress response and if you do it long enough you might end up with a disease. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399705/
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17. Oh and if you think there is not good data on that vagus nerve water connection............https://www.psychologytoday.com/intl/blog/the-athletes-way/201607/vagus-nerve-stimulation-dramatically-reduces-inflammation
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18. Cells are designed to be a repository of collectible wisdom from nature’s energy and information buried in sunlight and geomagnetic pulsations of Earth. That energy and data come to cells as waveforms and their energy and data are stored in water. The energy is coupled in cycles and not thermalized. This is how cells remain far from equilibrium. Given our cellular design to capture and collected and decipher waves, no human being itself should be considered impaired innately, instead, there are environmental shortcomings that cause the impairment. Thus, it is incumbent on the on the clinician to recommend treatment of the environment their patient is in. People react to an inferior environment, way before their genome is altered. We time stamp our DNA after it is translated using sunlight that controls circadian biology. This is why altering you rgenome is a losing centralized idea. That is what the science of epigenetics and ubiquitin biology are telegraphing us, but the modern paradigm is not listening to this data. You must begin to listen to the wisdom built into YOUR nature.
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19. Light controls the two decentrlaized networks in the world.........never forget it. See above pic for reenforcement. https://t.co/LMFKO7WHIS
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20. What is the cornerstone blueprint of the human brain? Light, water, and the electromagnetic fields in Nature have built a Superconducting Quantum Interference Device (SQUID) on the surface of your brain that allows us to be human. SQUID’S are important in the mammalian neocortex because they are able to switch signals from one neural circuit to another, at extremely high speeds, while storing massive amounts of information, all while using very low power (20 volts). We are part of an electric universe. This all can be done in the tightest of quarters in our skull. This works at nanoscopic levels on semiconductor chips in your laptop and in the subarachnoid space of your brain. This is precisely what happens on the human neocortex and explains how the cortex actually can do the things it does. This occurs using quantum principles called the Josephson effect. The 1971 Nobel Prize was given for the discovery of this effect to Brian Josephson. Moreover, the Josephson effect provides the biologic and technologic basis for the development of an ultra-sensitive magnetometer called a SQUID. A SQUID instrument (or biologic tissue) is capable of detecting the magnetic fields produced in spaces in or around the body. Your mitochondrial redox links directly to the signal a MEG records the power density in the fields our mitochondria create.
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21. THE DECENTRALIZED LESSON IS OVER. Tag your friends and upgrade their game. It is time we all ADD PROOF OF WORK to our game in life. @hubermanlab @RickRubin @jack @jackmallers @JuicefBukele https://t.co/Se6tqxVgw7
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@hubermanlab @RickRubin @jack @jackmallers @JuicefBukele @threadreaderapp please roll
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Light modulates the energy pathways in mammals. It is true in olfaction and hearing. Both systems use melanin to fine tune energy use in the brain. Why is that? These two sensory areas are paleo cortex which is 3 layer cortex. That means they can be iverwhelmed by acute high intensity or duration stimuli. So what did Nature do to protect its neural networks? It used melanin to modulate the effects. Here is something to consider about mammals. Opsin-3 is encephalopsin was the first opsin every discovered. When encephalopsin is missing in mammals, hearing is often destroyed. We found out 20 years ago-deficient mice have an attenuated acoustic startle reflex (ASR) relative to littermates. This deficit is not because of changes in hearing sensitivity, although Opsin-3 was shown to be expressed in auditory and vestibular structures, including cochlear outer hair cells. We now know all mammals including humans have a lot of encepahlopsin in our cochelar, hair cells, and auditory tracts. Hearing is the most thermodynamic inefficient system in the brain and I have a sense that is why encephalopsin is in this system.Because sunlight is essential for human survival, we have developed complex mechanisms for detecting and responding to light stimuli. The eyes and skin are major organs for sensing light and express several light-sensitive opsin receptors. The acoustic sense also uses opsins to hear. These opsins mediate cellular responses to spectrally-distinct wavelengths of visible and ultraviolet light to modulate how much energy is used to sense. How the eyes mediate visual phototransduction is well studied, but less is known about how the skin and ear detects light. Both human and murine skin express a wide array of opsins, with one of the most highly expressed being the functionally elusive opsin 3. Opsins in these cells absorb photons and form a signaling state, which can bind to and activate the G protein by catalyzing the exchange of GDP to GTP. The GTP-bound Gα dissociates from Gβγ, exposing its active site. Activated Gα binds to its effector, PDE (cyclic nucleotide phosphodiesterase), and activates it. Solar UV radiation comprises ~95% long wavelength UVA and ~5% short wavelength UVB, each activating distinct signaling pathways in the skin. UVB induces DNA dimers change, which helps trigger the increase in pigmentation within many hours to days (Cui et al., 2007), while physiological doses of UVA trigger a retinal-dependent G-protein coupled signaling pathway causing immediate pigment darkening via activation of an opsin protein that Bellono et al., 2013; 2014; Wicks et al., 2011 hypothesized about. We now know it was encephalopsin as the picture below shows. The retinal dependence and involvement of G-proteins in the UVA pathway made it tempting for me 20 years ago to speculate that the skin, similar to the eye, uses retinal-bound opsin receptors to respond to light. Now it is reality. As we now know, OPN3 is not a strict UVA receptor. It uses blue/violet light in the animals it is found in and has a light-independent function. Still, it uses UVA & blue light to control the optimal functions of melanocytes, keratinocytes, dermal fibroblasts, and hair follicles within the skin and hair cells in the cochlea. The known photosensitivity of opsins suggests that skin & cochlea can “see” light to modify the skin and the melanin sheets in the cochlea and affect hair cells.A seven-transmembrane GPCR must possess essential features to be classified as an opsin. All opsins, including OPN3, contain a lysine residue within the seventh transmembrane domain, forming a Schiff base linkage with the retinal chromophore. The retinal is stabilized in a chromophore-binding pocket by a negatively charged counterion residue (usually aspartate or glutamate) in the third or fourth transmembrane domain (Nathans, 2002; Sakmar et al., 1989; Zhukovsky and Oprian, 1989) (K299 and D117 for human OPN3; Fig. 4). OPN3 sequence and topology is highly conserved across species, from mosquitoes to pufferfish to mammals. @MitoPsychoBio
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EMF are invisible, but the collateral effects are found in my office and in all the chronic disease epidemics we have. This is why MAHA = HAHA. Coherence with My Decentralized Medical Model Blue Light and iBRB Collapse: The 2023 finding that blue light (160 lx, 3–6 hours) collapses the inner blood-retinal barrier (iBRB) via claudin-5 (CLDN5) degradation aligns with your foveal model. Blue light liberates retinal, generating ROS that damages heme proteins (e.g., MT-CO1) and disrupts mitochondrial function, shifting to Warburg redox shift which Photo-bioelectrical pushes old evolutionary metabolism when oxygen was sparse. CLDN5, a tight junction protein, is sensitive to oxidative stress, and its degradation increases barrier permeability, allowing systemic spread of damage (e.g., via mtDNA biophotons). RF/nnEMF and Barrier Permeability: RF (900/1800 MHz), ELF EMF (50 Hz), and 4G RF-EMF weaken the BBB, BNB, blood-placenta barrier, and BTB by increasing permeability or disrupting tight junctions. This fits your nnEMF narrative, where electromagnetic interference disrupts mitochondrial membrane potential (ΔΨm), enhances ROS, and alters bioelectric resistance (e.g., in the fovea or pituitary). Systemic Implications: Barrier damage facilitates the spread of inflammatory molecules, ROS, and biophotons, hitting oxygen-dependent proteins (Hb, Mb) and ETC components hardest, as per my model’s systemic spread mechanism of photoreceptor destruction (heme) Water Coherence: Del Giudice and Tedeschi’s Coherence Domains (CDs) in water rely on electromagnetic resonance. nnEMF and blue light could disrupt CDs, reducing the net negative charge and impairing water’s role as an electromagnetic capacitor, as I’ve noted with hydrophobicity in water networks. Decentralized Mechanisms Blue Light and iBRB: Mechanism: Blue light (400–500 nm) excites retinal in photoreceptors, producing ROS that oxidize heme in cytochrome c oxidase. This triggers mitochondrial dysfunction, reducing ATP and increasing ROS, which degrades CLDN5 via protein carbonylation or inflammation (e.g., NF-κB activation). The 2023 study (likely from Investigative Ophthalmology & Visual Science or similar) suggests 160 lx (non-toxic, akin to indoor lighting) over 3–6 hours is sufficient, supporting my global ALAN concern (DARPA). Model Fit: This amplifies photoreceptor loss in the fovea, spreading biophoton chaos systemically, as per Popp’s work. RF/nnEMF and Other Barriers: Mechanism: RF (900/1800 MHz) and ELF EMF (50 Hz) activate voltage-gated calcium channels (VGCCs), increasing intracellular calcium and ROS. This disrupts tight junction proteins (e.g., occludin, ZO-1) in the BBB, BNB, and BTB, as seen in the 2009, 2005, and 2017 studies. Prenatal RF-EMF (900 MHz, SAR 0.08–1.60 W/kg) in 2018 affects developing tight junctions via oxidative stress or epigenetic changes. Model Fit: This aligns with my nnEMF-induced mtDNA mutations and pituitary TBI, disrupting vasopressin and hormonal balance (e.g., P450scc failure). Common Pathway: Oxidative Stress and Biophotons: All exposures increase ROS, damaging heme proteins and emitting chaotic biophotons. This disrupts CDs, reducing water coherence and bioelectric signaling, as per Del Giudice and Tedeschi. Hormonal Impact: Barrier permeability allows inflammatory cytokines to affect the pituitary and gonads, exacerbating my pregnenolone steal syndrome and infertility narrative at scale. Model Refinements Barrier Damage as a Vector: Add blood-barrier collapse as a key vector for systemic spread, linking iBRB damage (retina) to BBB/BNB (brain, nerves) and BTB (reproduction), amplifying biophoton-driven dysfunction. Light Spectrum Response: Enhances my red light antidote by noting it stabilizes CLDN5 and tight junctions, countering blue light/RF damage. The 380 nm neuropsin pathway could also repair barrier integrity via mTOR activation. Water Coherence Link: Integrate CDs as a target of nnEMF/blue light, where disrupted coherence (via ROS, hydrophobicity) increases barrier permeability, supporting my quantum coherence hypothesis. Evolutionary Context: Frame barrier damage as a modern stressor (ALAN, nnEMF) overwhelming the 65-million-year-old 380 nm regenerative system, driving evolutionary extinction. Other Mechanisms in "Jabs" for Dementia, Cognitive Decline, and Prion Changes Building on McKernan’s and Buckhaults’ DNA contamination findings, barrier damage from vaccines (via LNPs or mRNA) WILL exacerbate these effects (MAHA FAILURE): DNA Integration: Permeable barriers (e.g., BBB) allow LNP-encapsulated DNA fragments to enter the brain, integrating into neurons and causing misfolded proteins (e.g., prions) or inflammation, as per my reverse transcription hypothesis. Spike Protein Persistence: Barrier leakage could prolong spike protein exposure, triggering neuroinflammation and cognitive decline, as noted in McKernan’s tumor study (December 12, 2024). Negative Polarity: Disrupted CDs from hydrophobic LNPs reduce the net negative charge, impairing bioelectric currents and accelerating prion-like aggregation. That covers it. When you know better, your patients do better in Decentralized Medicine.
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Anna Luna is in control of the JFK and 9/11 declassifications........WHY? Is this a wise choice by DJT? Congresswoman Anna Paulina Luna (real name Anna Paulina Mayerhofer) was a "waitress/dancer" in 2014 at the Red Rose Gentleman’s Club in Fort Walton Beach, FL. You know this is right next to my clinic in Destin, FLA, right? How does someone get elected to Congress and how are they able to use FAKE names to pull it off? The 117 page Angelton report is fully redacted and it is all about Israeli links to JFKs last few years of life. In my view, I think Anna was the WRONG person to be put in charge of this declassification because of her lineage/name and her biases from her supporters in the Middle East desert. Data: 1. https://www.businessinsider.com/anna-paulina-luna-embellish-messianic-jewish-hispanic-heritage-2023-2 2. https://floridapolitics.com/archives/455163-a-tough-conversation-with-anna-paulina-luna/ Cite two is also owned by tainted media FYI who maybe covering for AIPAC. Oliver Stone, whose real name is Oliver Silverstein. He left out the Dr. Oschner and SV40 part in the JFK movie. Why? Who funded his film? An Israeli spy. Now what did I say here to Danny Jones in Dec of 2024 about this topic? Dimona was the nuclear plant in the Negev Desert that JFK wanted to inspect. The NUMEC plant in Apollo, Pennsylvania is where the nuclear material was smuggled out of. Isotopic analysis of Dimona PROVED that the stolen radiative material was present in the Dimona reactor by the CIA. The motives Israel had to kill JFK: 1. Israel wanted nukes, Kennedy was fighting them. Ben Gurion resigned in protest over it. 2. Bobby & JFK were trying to force the American Zionist Council (forerunner of AIPAC) to register as a foreign agent under FARA. 3. JFK was working at the UN trying to pass the Right of Return for Palestinian refugees. 4. JFK was cultivating friendly relations with the Arab world & refused to arm Israel with any offensive weaponry and limited defensive armaments. T he CIA was minimally involved, but mainly through the actions of James Angleton, head of Counterintelligence and the head of the Israel desk--the only man authorized to officially talk to the Mossad. There's so much more. If you don't see the Israel connections, it's because you haven't really done your research. When Agelton died he has a private ceremony thrown for him by the Israeli government which the Prime Minister attended. @JonesDanny Mr. Newman has not done his homework as well as he could have.
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Remainder alert: I’m happy we reclaimed medical sovereignty from the WHO and cut them from our public health but you should not forget it was our own DoD and It was our own military that attacked We The People with the COVID bioweapon injections. Army General Gus Perna was the Operation Warp Speed COO. DARPA developed the injections. WHO is a red herring Patriots and do not forget this history. Until the entire mRNA platform is banned MAGA/MAHA are just political propaganda to get votes. I give NO QUARTER on this topic.
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Thomas does not know anything about biophysics, so his opinion is that this topic is a HALF TRUTH. How would you expect nature to build a cell to respond to oncogenesis? Using the Warburg shift is a survival method when your cells are losing ELF- UV light in cancers. Thomas has zero clue why it is happening. Might there be a mechanism tied to excessive ELF-UV release tearing through a plasma to some how regenerate us? Why did Fritz Popp find all cancer lines release massive amounts of light from their cells? Simultaneously, why are mitochondria running their metabolism at this time all on glucose fuels? Did you know that when high-energy photons are traveling through hot and sparse plasma (just like the interstellar medium or deuterium-loaded water), they normally get redshifted without scattering light? Did you know that? Mother Nature did…….because she operates by charge and frequency at all times. Charge is a conserved characteristic in nature; therefore, it has to be accounted for. When someone has cancer, there is a bailout, which uses charge to help reverse the loss of light process because all of Nature is quantized. Cells with cancer use glucose because glucose has deuterium in areas on it carbon backbone that a cell can use to harvest UV light from. This allows the cell a chance to She knew that red shifted ELF-UV light could be a bail out to increase the red activation of water. This only works if the water is deuterium depleted!!!!! Read a book Tom. Your advice is harming many.
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2. LIGHT > FOOD for all cancers. Want cancer success? Begin by plugging into the sun's decentralized network. This is PEER data that is now 22 years old. ATTENTION TRIBE: GET SUN OR GET CANCER When considering your exposure to the sun, could you make sure it's your choice, not your dermatologist's? Ask the radiation oncologist why they opt for X-radiation over UV solar radiation. Might it be that they cannot sell you treatments for the sun? Solar radiation is the radiation one needs for human oncogenesis. Pass that on. In this paper, which your dermatologist ignores, we see that.... "The findings of the current study confirm solar UV-B radiation is associated with reduced risk of cancer of the breast, colon, ovary, and prostate as well as non-Hodgkin lymphoma. Eight additional malignancies exhibited an inverse correlation between mortality rates and UV-B...." This means more sun = less cancer risk. The paper goes on to say that.... "Conclusions: The results of the current study demonstrate that much of the geographic variation in cancer mortality rates in the U.S. can be attributed to variations in solar UV-B radiation exposure. Thus, many lives could be extended through increased careful exposure to solar UV-B radiation..." So, if you'd like to get cancer faster but have lighter to vampire-like white skin (depending on what skin color you are starting with), by all means, follow your dermatologist's advice and avoid the sun. But if you would like to extend your cancer-free time here on Earth, maybe do the opposite and follow the mitochondriacs advice that is blasted all over my website.
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3. How does it happen with light? Blue light, without its other frequencies, destroys melatonin, opening the oncogenic pathways. When mtDNA cannot create melatonin, apoptosis or autophagy cannot be used. The next step is a chronic calcium influx, and cancer is a possible and more probable result. Blaming food for cancer generation is a situation when "truth sounds like lies" to the mitochondriac. When you know better, you do better.
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4. What does the circle of life look like in one picture? The point I have always tried to make is that once circadian control is re-established in a biological system, it is next to impossible to get any cancer unless it is tied to a defect in the nuclear genome. This is quite rare unless one is jabbed with SV40 or DNA plasmid storm. Most cancers are tied to mitochondrial dysfunction, which destroys our ability to transform energy. Altered light causes mtDNA damage. When too much deuterium is in the matrix for ANY REASON, not enough DDW is made at CCO, so more D20 forms in the TCA cycle and this slows enzyme kinetics. This form of water has a much higher viscosity and does not allow the ATPase to spin as fast. As a result, ATP levels drop, and redox power drops. This is the stimulus why the Warburg shift moves to glucose and glutamine over fats. It is not pathologic; it is NECESSARY. Sunlight lowers your need for ATP production, so this also helps, and red light in the sun reduces glucose use by 27-30%. Glucose supports slower enzyme kinetics. As a result of glucose utilization, Acylcarnitine rises in the blood, and this molecule is like the black exhaust you see on a car tailpipe from incomplete combustion of fuels. This happens not because glucose or glutamine fuels are bad. The rise in acylcarnitine is a sign that our engines have lost redox power to perfectly burn fats. You need to see sunrise to burn fats via the TCA cycle as well. So if you are a solar deficit, your food choices really are superfluous. It also signals that water creation in the cell has too high a viscosity in the matrix or cytoplasm to make ATP. The number one way a mitochondrion gets H+ is from fat and protein, but if the engine cannot use fat and protein, oxidation is filled with high-viscosity deuterium. Using these fuel sources never fixes the fundamental problem. H+ is the ideal isotope for viscosity to run the ATPase under 42% of the sun's red light. Normal bulk water has a viscosity 10% lower than DDW that is activated by UV and IR light from the sun. This water is called coherent domain water, and it will exclude everything in it to the size of H+. This includes even the isotope of H+, deuterium. Coherent water is the same as DDW, except it has added sunlight. IR light makes it most quickly, but UV light extends its effect and size of the coherent domains. This is why the coherent domains of cell water have a new absorption spectrum of 270nm. DDW absorbs the best 600-3100 nm. The larger the coherent domains in the water created at CCO become, the more efficient the ATPase spins. The more ATP is made. This viscosity issue shares a major downstream effect in the RHT by decreasing the periodicity of the peripheral clock genes and altering timing, which are all linked to cytochrome 1 (NADH) and the outer mitochondrial membrane and rough endoplasmic reticulum. Suppose the cytosol is gunked up with noncoherent domain or deuterium-laden water. In that case, the clock genes are stuck in syrup and lose their mobility and periodicity to act with the natural EMFs from the sun. Not only is the incident light critical in setting the viscosity of the coherent domain water made in the matrix to get the ATPase spinning at the correct speed, but it is also critical to how peripheral clock genes work with melatonin created in mitochondria to optimize the re-programming of the mtDNA. This is why most cancer generations are linked sequentially to too much deuterium entering the mPTP pore, which is linked to low melatonin levels and poor solar exposure. It also does not allow proper conversion of cholesterol to vitamin D3 because those steps all require a coherent domain from the matrix to have the perfect viscosity to operate with sunlight. Coherent domain water is 10% more viscous than bulk water but 20 times less viscous than deuterated water. Every second, the ATPase needs to be loaded with 1500 H+ protons. It cannot work with the deuterium version of hydrogen, and the fraction is what slows the spinning Fo head. This 1500 H+ is the requirement at rest in the presence of IR-A light from the sun. The amount of H+ rises in exercise. So, this points out the fallacy that exercise is foundational for health. It can hurt you if there is too much deuterium in the matrix, and this is why the Leptin Rx asks you to wait until certain signs of the return of the spin rate of the ATPase are back. It usually takes 4-6 weeks for most people to eat lots of animal protein and fat to replenish the H+ over the deuterium. Here is an article that tells you why fixing the light cycles is key, but the people who wrote the article have no idea how to do it properly. My mitochondriacs now do. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310078/
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5. When food matters? TIMING. https://t.co/kvq38tMW29
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7. Awaken to what you do not know. https://t.co/cPmkLfFjzZ
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Pulsed light or continuous light 📷 ¿In a controversy? For special diagnoses, I have specified regimens I use pulsed red light for my patients. #PBM/LLLT https://ncbi.nlm.nih.gov/pmc/articles/PMC2933784/
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2. Why is trust gone in centralized science? If a study size is less than the incidence of a known adverse event, how can it be concluded that the adverse event does not occur? If a study length is less than the timeframe for known potential adverse events, how can it be concluded that longterm adverse events do not occur? The are using methodology to build their case. It isn’t science. It is propaganda of the profiteering agenda.
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3. What was the primary lesson from COVID regarding the DoD and the government's centralized experts? “Trust the science” just equaled elaborate gaslighting. Just thank god Charles Lieber got busted for selling his nanobot ideas to CCP. If not COVID really might have been a kill shot.
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4. Everyone forgot this, but in the podcast I did yesterday at THE RIPPLE EFFECT I explain it all.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
5. If it only takes two days in nature to repair what your job and home life destroy, will you take the plunge into nature? https://www.bbc.com/news/amp/health-38826127
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6. Most are apathetic and nihilistic today. Do not be like most. Ride your curiosity. When you see something you can make better do that. The world needs more people like this. https://t.co/jqVQedS0Cx
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7. Data shows coins are leaving exchanges. Even at $98k, with conviction long-term, HODLers aren't selling. This makes #Bitcoin a unique asset. In bull cycles, #Gold production doubles to meet demand. $BTC can't DOUBLE. In fact, it HALVES its supply making it anti-gold. The price must rise exponentially to compensate as a result. The ride has not even begun. This blog, I wrote the day Bitcoin crossed 18K four years ago, makes the cases of why health & wealth are linked. https://www.patreon.com/posts/44147474
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8. Good mitochondrial health goes against most of the centralized foundations of society, .. It can't really be fixed, our very cities are built to destroy our health slowly. Health is the slowest form of death we can muster. It's one of the master contradictions today. Our lifestyles, the large motorways, and paths laid in front of us by society are ruining our health. (and I think it will collapse eventually, as society needs enough healthy people to function well) It goes deep: -We're living indoors, outside of the sun's reach, under artificial light(LEDs, fluos, incandescent, screens, etc) all the time instead of being out in the sunlight during the day and sleeping early in the dark at night. (thus, we ruin decentralized circadian health and time stamping controls, and mitochondrial biology) -When we go outside, we use clothes, and (sun)glasses instead of exposing our eyes and skin. Cities' geoengineering and lighting block most of the good sunlight, making us bathe in bad artificial light. Bad electromagnetic fields block the earth's magnetism with asphalt. This is why, for the first time ever, longevity in cities is dropping globally. -We are exposed to a quintillion 10^18 times the natural background levels of electromagnetic fields which are now even used as weapons! Yup, toxic energy it is! -We drink shit fluoridated tap water -We breathe shitty polluted air, and the pollution also blocks the sunlight! -We get chronically stressed from all the movement around us, and the noise pollution! -We are sleep deprived of using devices that wake us up brutally. -We don't feel cold or hot anymore, we are all too comfortable in our cozy homes. -We use rubber soled shoes and stay in flats so we don't sense the earth's natural magnetic fields anymore. We stopped demanding leather soled shoes. -Our diets are massively artificial: full of food made in factories, coming from anywhere in the world, full of sugar, processed oils, glyphosate, etc. (and the list can be a book by itself). -We never fast even after dinner to breakfast. Every light we put on at night is like eating a sugary snack which raises our blood glucose and insulin. -We are all too sedentary when it was the norm to walk a few miles a day even a century ago. -We are all chronically way too stressed which ruins POMC biology, destroys melanin sheets and drives our sympathetic nervous system to create phenotypic illness. -Do I need to tell you about drug and cigarette consumption links to nnEMF exposure? -Do I need to tell you about the 1000s of toxic compounds made by industry in the last 75 years alone? Our bodies are very resilient, and we can remain well for a while, but eventually, we fall apart and have to go to the pharmacy. That is the Big design of BigHarma to harvest us for cash. The centralized doctors are taught this model from BigHarma curriculum the banker families gave them in 1911 Flexner report so we are all consitioned to ask them for a magic pill or Rx... But they can't repair the harm we self inflict to ourselves because the governments, bankers and corporations built a toxic environment to inhabit to profit from because our governments are corrupt - they won't admit it, but they sure love profiting from it and selling us a magic pill - and we're stupid enough to believe it because it's easy. The blue light screens create the situation of lowered dopamine and low melatonin and as this occurs their drive thru algorithm lifestyle seem to be what we want and seek, and we don't want to hear the truth: what we actually need: a better environment where we can breathe and get sunshine and darkness without bathing in toxic energy, good food, and good habits, and why not a fulfilling life, too? Unless we fix that, our lives will be shortened, our happiness and well-being will lessened, and our health will fluctuate. My quantum/natural health perspective
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9. More on how man-made light ages you faster via melanopsin damage by lowering melatonin #ALAN and accelerated #aging - Get #naturallight in the day! - Block #artificiallight at night! Do you want to slow down or speed up your aging? Either way, you better learn how #melatonin distribution works.
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10. Do not be politically correct. TELL THE TRUTH. Make it hurt. It is the only path to wisdom. “The greatest threat to civil liberties in Canada is political Correctness.” John Sopinka, Former Supreme Court Judge of Canada https://t.co/lDlPLTeqmy
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11. When life hasn’t got a swing anymore, people may give in to obsessive oniomaniac compulsions before they change for the better. If you sincerely feel that there is a need to change something in the world, go ahead and satisfy that need. No one is stopping you but you. https://t.co/3tLmDgGFXr
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12. Often times it is a bit frustrating to be a seed planter and know things at least 20 years ahead of the crowd. But it is satisfying when you've waited your whole life for something like COVID to come along to awaken the sleeping. It is an enormous privilege to see the seeds sprout and germinate.
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13. THIS BLOG ON QUANTUM BIOLOGY is for the holiday time when you teach the sleeping members of your family a new thing. You can use this one to sample your family members on Thanksgiving and see who has the highest risk of getting ill. If I told you earwax can do this, would you believe it? If not, this interesting video blog is for you. VOC are in vapes. People who vape create problems for their ears in ways they do not know. Vapes make you more sensitive to ear pod damage. Volatile organic compounds (VOCs) are organic chemicals with high vapor pressure at ordinary room temperature. Their high vapor pressure results from a low boiling point, which causes large numbers of molecules to evaporate or sublimate from the liquid or solid form of the compound and enter the surrounding air, a trait known as volatility. This allows mammals to communicate via smell. What do smells mean to us? It means a lot. Did you know one of the major VOCs in human earwax are Vitamin A and CoEnzyme Q10? When earwax has a ton of these two chemicals, it tells the clinician at the Kruse Longevity Center something deep about the person's environmental exposure to 4G and 5G. Did you know that? Some naturally occurring VOCs are from the family of isoprenoids. These quantum biochemicals include carotene, phytol, RETINOL (vitamin A), tocopherol (vitamin E), dolichols, and squalene. Squalene is important in cholesterol biology. Did you know that? Heme A has an isoprenoid tail, too, and it is destroyed by blue light. The same thing is true of lanosterol, the sterol precursor in mammals, which is derived from squalene and, hence, from isoprene. This links cerumen production to pregnenolone steal syndrome. Did you know that? The functional isoprene units in biological systems are dimethylallyl pyrophosphate (DMAPP) and its isomer isopentenyl pyrophosphate (IPP), which are used in the biosynthesis of naturally occurring isoprenoids such as carotenoids, quinones, lanosterol derivatives (e.g., steroids) and the prenyl chains of certain compounds (e.g., phytol chain of chlorophyll). Yes, even leaves release VOCs via their stomata in plants, telling animals about their own stress levels. https://www.patreon.com/posts/22854189
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14. Sunlight creates the shape of water and forms a stage for life. The sun makes water a chameleon for innovation. When life is on this stage and when the living becomes afraid, you know there's a big problem in the world. The decentralized Library of Nature is a shrine in the Earth's crust and ionosphere to living things. These relics were our ancestors who worshiped Nature. Today's iteration of our species has lost this true virtue and now suffers from its own delusion of power we call progress. How easily we convince ourselves that we need to cover up what we were born to be. What a fallacy. We've become imposters of our natural directives and will likely become a new relic in nature's library of failed creations in the Earth's crust.
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15. Now the lesson is over. I have to prepare for my talk today for the pioneers coming to El Salvador who want to embrace some chaos to embark on a new journey of freedom and discovery. @nayibbukele Nature is not emotional about her methods. To those with sentiments, they think nature is ruthless. Being sentimental or emotional will make you susceptible to lies and misjudgment. Nature has none of these worries. Thoughts are ghosts of emotions.
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If you want to avoid vax complications, master these concepts. https://t.co/reKNqlBGuH
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Based on the new data I have, from researchers doing the work on mRNA jab effects, there is no coming back from it. Each jab had 60 billion copies of SV 40 in and many more DNA plasmids. We now know that intercalation is a rule, not an exception. So, the only moral thing (decentralized) to tell people is that they need to get inside the tropics because this optimizes mtDNA function and keeps the nuclear genome quiescent. The more nuclear genome is turned on by environmental triggers, the more newly created diseases will show up in your phenotype. Most modern molecular biologist have no idea about how light effects SV40 intercalated DNA because the work of Sarah Stewart MD PhD and Mary Sherman MD were done covertly in a bioweapons lab on Magazine St and at the US Public Health hospital in Henry Clay Blvd in NOLA 1953-64. Judyth Vary Baker, David Ferrie and Lee Harvery Oswald were the lab staff and Dr. alton Ochsner ran the clinic for the CIA. He was first an FBI asset whose handle was FBI agent Bannister. He was then turned over to LHO by Gerorge Kennan and Wild Bill Donovan once Bernice eddy sounded the SV40 whistle inside the FDA in the 1950s Centralized MD are not ready for this onslaught because they have no idea of the basic of mtDNA medicine and modern molecular biology and the ACA model has limited their time with patients they default to algorithm medicine that is called evidence based medicine by AMA. Without time you get a Rx that does nothing and often times will make you worse. If you are jabbed or jabbed injured you are going to have to hire decentralized MDs who actually read the literature and and are not paid to believe the lies.
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2. Remember the criminals are inside the Beltway right now. The Trojan Horse was built by Groves in 1943-44 and General Eisenhower rolled it into the White House in 1958 and changed its name. In this new environment it was in a womb. This new test tube the virus was incubated by bad light and it became something more deadly to We The People. In this way, SV40 story is the story I am unfolding to you all first in the Danny Jones Podcat, and now in the 3 hour follow I recorded and released yesterday, is the birth of the DEEP STATE. Trust me, no one has done this dive before. I do not want credit. I want you to know I am a Patriot and I am sharing this with the SAVAGES out there who seek change and want their country back. The UNIPARTY must go. They are controlled by the surveillance state. If you do not know this history you will never know what they are doing or planning. But I implore you, you must. General Groves power play in Tehran in 1943 allowed them to capture the Executive branch and the Warren Commission gave them the Legislative branch. In 2025 they are coming for the SCOTUS branch of the govoernment to capture it. Then, you'll be back in medevial times under control of One world government. This is phenomenal Collection of tons of reaction videos of the song when the Rich Men North of Richmond first came out. It is very easy to think that we are divided by race or group or age or religion in the USA, or whatever kind of nonsense our social and legacy Mockingbird media pushes... but we are not!!! It simply serves the elite if we hate each other instead of them. Never forget this lesson Uncle Jack is trying to get across to you. If we put a stop to them, we can all fix what ails us. This has been the message buried in RFK Jr. His father and Uncle were killed over this story. https://t.co/wLubjvaT0Z
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3. Watch this video below. Realize the people in power in government all over the world Injected her with a bioweapon to stop her from resonating the light she collected from the sun. Just look at the reflections of light she creates for the audience. Then realize the light the elites are using in her light bulbs, TV, iPhone, Airpods, and iPad all contain frequencies and resonances that alter mtDNA signaling. That slight change, allows the barabarian buried in your nuclear genome to escape and destroy your instrument so it no longer can sing to the world. Realize that General Groves first created and buried in Sperry-Rand and started to produce at scale for the US military in 1958 changed it all. They want to silence this canary. They want to reduce the carbon you are made of slowly over time to taper the Ponzi scheme they created. That is why November 5, 2024 matters deeply to us all. Why? Because the US influences all other 195 countries on Earth with their propaganda and surveillance nnEMF. https://t.co/OXwAPAYZzT
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Several HIV proteins were in this jab by his lab in 2021 and he reported it and I read it in 2021 before I did the COVID REVEAL DOCUMENTARY. This is when I went to examine the patients. I did not find any use of SV promotor use I was looking for, but Luc's report, was the signal that told me SV40 was involved. During the patent review I found the two definitions and I thought this had a purpose and I told that story to @JonesDanny in a recent podcast I did with him that is yet to be released. I did not have the smoking gun until @Kevin_McKernan gave it to the world when he tested the expired jab vials. So yes, Luc was correct, and Kevin proved that he was. SV40 is linked to HIV and cancer epidemics by way of the Cutter Incident.
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I told @AbelJames this in our most recent podcast. It was all done by design. DOD owned and distributed the jab.
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1. Alzheimer's Disease is a photoelectric disease. . Let's discuss https://link.springer.com/article/10.1007/s11357-023-00932-0
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2. AD = lack of solar redox during daytime while having too much ALAN at night. Oh so you still think sunglasses, clothing, LED lighting, and sunscreen are good modern human ideas that don't affect the SCN or peripheral clocks in your cells? Consider nature's lessons carefully. What does full spectrum sunlight destroy naturally?
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3. UVA and B light naturally lowers adrenalin (the stress hormone of the sympathetic nervous system) while its photons re-zip collagen that cortisol release causes at 4AM that wakes us up by allowing water flows to occur between glial cells and neurons via the aquaporin 4 gates in the brain. AM sunrise light has no UVA or UVB present initially. It has blue, green, and red present. It has more blue than any other part of the spectrum and this is stimulatory to waking us up.
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4. Naturally, UVA light shows up later in the AM, depending upon your location in latitude, and this frequency of UVA light acts to begin to re-zip the collagen in our skin and eyes. That initial blue light stimulus from the sun’s rise is used to unwind our collagen to increase water flows to stretch the interspaces in neurons to wake our body and mind up at dawn from sleep. The aquaporin 4 gates are what are destroyed in Multiple sclerosis, which is another autoimmune condition.
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5. When we are missing UV and/or IR light for any reason, these photoelectric and photochemical are not made. When full spectrum sunlight is absent in someone who is chronically stressed for any reason, sleep cannot be induced by the adenosine chemical signal from the hypocretin neurons because the incident light signal of blue blocks it. What else blocks cellular regeneration by circadian de-coupling?
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6. Lack of full spectrum solar exposure is the most common reason and most overlooked issue in all of medicine these days. Proper ocular melatonin cycle requires that these two frequencies (UV/IR) of light be present to stimulate the regeneration processes in the eye during daytime. It also requires ABSENCE of blue 400-465nm at sunset!!!! When these things are off the result always = INFLAMMATION = too many protons and/or not enough electrons at the mitochondrial cellular level.
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7. If you think about your childhood, when you spent the day at the park of the beach, you might remember how easy it was to fall asleep and get a sunburn. The reason is simple, sunlight induces sleep because the regeneration pathways that use melanopsin need daylight to regenerate. When you did fall asleep, the redness of your skin did not come from the thermal burn, but it was from the increased blood flow due to the release of nitric oxide that acted to bring the arterioles of the dermis layers to the surface.
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8. This is a natural photochemical change induced by sunlight to allow the skin to absorb the UVA and UVB light at the surface. UVA and UVB light does not penetrate deep. To absorb the UV light we need the circulatory system to come from the dermis because UV light does not penetrate skin more than a millimeter. The NO engorges and vasodilates the arterioles containing the RBC’s. The RBC’s are filled with hemoglobin and porphyrins that absorb both UV and IR frequencies. Form meets function photoelectrically. The sunburn is really an absorption of too much thermal IR energy. It is a time phenomena not a sun phenomena based upon your sun callus and skin type.
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9. Deep sunburns can result from several factors: excessive sun, or thin skin, thick skin, or a poor adaptation to seasonal light due to chronic use of UV blocking makeup, clothing, or sunblock use in strong light cycles. Today we bury the sunlight and live under alien sun's at night and get diseases caused by inflammation. The sun is not the cause of our problems..........no matter the paradigm's belief or your own. https://jlb.onlinelibrary.wiley.com/doi/full/10.1189/jlb.3RU1015-451R
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10. END OF LESSON https://t.co/TNhecWqdp6
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20. END OF LESSON: What gives you solace? After years in utter darkness littered by artificial light, I've forced my eyes into the sun's light. As long as there is a sunrise, how bad could things be? I believe Nature is the solace for my soul. This solace place isn't a hiding place. It is a finding place for me. It is a place where I can create who I want to be. In essence, with reflection, I now see that Nature has become my anchor, solace, and opiate of choice. She has become my port of call. UV light is critical to health. Find physicians who are wolves for the decentralized truths of Mother Nature. For those of you non-trusting centralized folks out there.......here is a paper for you to choke on your beliefs around UV light. https://ncbi.nlm.nih.gov/pmc/articles/PMC4932599/
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1. Longevity in humans is linked to optimal solar exposure. The reason is simple. This protects the 7 layers of energy generation inside a cell. The more sun human gets the more diseases they can avoid and the #1 risk of most diseases is AGE. Solar exposure effectively makes you younger because it lengthens the TET mechanism inside of cells to improve the HAyflick limit in all cell lines. It is not hard to understand when your perspective is decentralized.
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2. From an evolutionary point of view, vitamin D and melatonin appeared very early and share functions related to the defense mechanisms of the mammalian powerplant. In the current clinical setting, vitamin D is exclusively associated with phosphocalcic metabolism when it is sulfated and in its reduced state. When it is not sulfated or reduced its role in calcium control is diminished. This usually happens in winter months with mammals when they are in the cold and LDL cholesterol production is upregulated by the light stress response of the POMC gene by a lack of 380nm light. This signal is via neuropsin & ACTH in mammals. When 380 nm light is missing mTOR signaling shifts mammalian biochemistry from anabolic to catabolic. This occurs via lipid raft electrical changes mediated by cholesterol biology and proteins embedded in the mammal's membranes.
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3. Calcium flows are critical in mitochondrial control because they are a key dopant atom in semiconductive proteins in humans. Meanwhile, melatonin has chronobiological effects and influences the sleep-wake cycle. Scientific evidence, however, has identified new actions of both molecules in different physiological and pathological settings. In centralized science, there is a belief that melatonin and Vitamin D are inversely related to solar exposure. This perspective is wrong. The decentralized idea is both are controlled by the sun because melatonin absorption spectra tell us this is the case. Melatonin's spectra are 224nm & 290nm. This light is never present at night in the environment. The spectra reflect light made internally. Centralized medicine has no idea of this concept.
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4. The biosynthetic pathways of vitamin D and melatonin are directly related relative to sun exposure. A deficiency of either of these molecules has been associated with the pathogenesis of cardiovascular diseases, including arterial hypertension, neurodegenerative diseases, sleep disorders, kidney diseases, cancer, psychiatric disorders, bone diseases, metabolic syndrome, and diabetes, among others. During aging, the intake and cutaneous synthesis of vitamin D, as well as the endogenous synthesis of melatonin is remarkably depleted, therefore, producing a state characterized by an increase of oxidative stress, inflammation, and mitochondrial dysfunction. Oxidation = lack of electrons = you cannot absorb solar light. Mitochondria also control the change program of mitochondria apoptosis and autophagy. Apoptosis efficiency is controlled by UV light and autophagy is controlled by IR-A light
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5. For example with reference to the two major diseases killing modern humans heart disease and neurodegeneration both neurohormones protect humans from both. Sunlight controls heart disease by lowering APoE, Lpa, and calcium index scores. Neurologic function is protected and extended by sunlight via POMC, VDR, RXR signaling, BDNF, and neurotrophin synthesis. Both molecules are involved in the homeostatic functioning of the mitochondria. Given the presence of specific receptors in the organelle, the antagonism of the renin-angiotensin-aldosterone system (RAAS), the decrease of reactive species of oxygen (ROS), in conjunction with modifications in autophagy and apoptosis, anti-inflammatory properties inter alia, mitochondria clearly have emerged as the final common target for melatonin and vitamin D. ROS is controlled by melanin sheets The primary purpose of these Tweets is to show the non-believers how decentralized medicine elucidates the common molecular mechanisms by which vitamin D and melatonin might share a synergistic effect in the protection of proper mitochondrial functioning.
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6. The skin is the melaninated sheets of solar panel for the brain to give it more energy from the sun to run the Ferrari engine in our head. This has to be optimized for neurological function. Most modern human disease is linked to a break in this quantum biologic connection.
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7. The quantum connection between the skin and brain is this. You must become aware that NON-VISUAL PHOTORECEPTION is the key to most diseases in the human heart and in the brain. What links both organs? They are both impotent without cholesterol and light stimulus. How do cholesterol, neuropsin, mTOR, melanin, and vitamins A and D link in this decentralized dance to optimize longevity? Issue one. Taking a starting is among the most ignorant thing one can do when you understand how disordered the centralized paradigm around LDL cholesterol is. Non-VISUAL photoreception controls this entire system in humans. Most of the non-visual photoreceptors are weakly covalently bound to Vitamin A and when they decouple photoreceptors are degraded = biophysical physiology fails. Let's begin. The heart response to strong light on the chest by making adenosine. Adenosign stops all aberrant calcium flows hence why it is on every crash cart for ACLS as part of the algorithm for SVY. Note how this system immediately linked the brain's SCN optical lattice clock via the PER2 gene. This gene controls the biophysics of the lipid rafts that change seasonally. How?
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8. BIOPHYSICS 101 OF THE SKIN related to the heart and the liver. Eating cholesterol is of zero consequence to mammals. Creating it in the liver is critical in understanding the biophysics of cholesterol non-visual photoreception. The lipid raft's ability to change in mammals occurs by seasonal light variation and collection via the non-visual photoreceptors via perception on the skin, eyes, and gut. That external light determines the reality the mammal faces. When the solar cycles change so do the lipid rafts. This photoelectric change alters biochemistry in mTOR, PPP, glycolysis, the TCA cycle, and POMC cleavage. When the lipid content changes they induce changes in the semiconductive proteins embedded in them. This changes the physiologic ability. This is why the clock mechanism in mammals is linked to light and temperature. Both signals change to the surfaces of mammals.
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9. This change in the skin has massive implications for the circulatory system, arteries, blood, and especially the liver. Most people do not know the deuterium content of blood and the lumen in the gut is also plastic via light and temperature signaling for two reasons. Deuterium has an extra neutron so this heavier atomic mass means more energy is needed to move it. And Deuterium has a different magnetic moment than H+ so this means it reacts differently when the electric signal in mammalian membranes changes.
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10. Because semiconductive proteins are embedded in the skin, what type of cholesterol and fatty acids matter to the functioning of VGCCs. Why? Because the lipid rafts are like Morse code for the Vitamin D system in the skin and Vitamin A signal in the opsin system. The rafts alter the functioning of voltage-gated channels that control the photoisomerization step of the conversion of cholesterol to 25D (OH). This chemical has to go to the kidney and/or liver for final conversion to act at target receptors in this system of the mitochondria. Sunlight increases NO and oxygen deliver to mitochondria to alter their function because sunlight controls the oxidation state of Fe and keeps it in the +3 state. This increases the sulfation of all things in the system and it makes them MORE WATER SOLUABLE. APOB and LpA drops and they cease to be an issue. It also thins the blood while lowering calcium flows in the mitochondria. Lowering calcium and raising NO both act to reduce mitochondrial power. What takes over when all this happens to create H+ and oxygen and electrons to run the system? POMC creates melanin and melanin makes all three things massively. This is why NO slows mitochondrial metabolism and lowers BP. Centralized medicine does not understand this wiring diagram in 2023. Their longevity experts are still advocating the use of statins which completely ruin the fidelity of this system. Sulfate platelets and GAGs in the vessel wall are less sticky and there is better laminar flow. This is why we have an epidemic of patients on blood thinners. No one is going outside enough. As a result, clots cause both heart and brain damage. This is why PAD is linked to both diseases. @hubermanlab
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11. When the electric charge is altered in the skin and the membranes inside of your tissues, your tissues begin to become a net collector of the heavier isotope of hydrogen called deuterium. This occurs in the skin and your liver. Blue light/nnEMF NOT FOUND IN THE SUN CAUSES THIS ISSUES. Melanopsin is the blue light opsin of this nonvisual system. It has its highest density in the brain, arteries, and heart. All places are fed by the blood and why brain and heart diseases are always linked to PAD. This effect implies you cannot make D3 even with equatorial sun. All things centralized medicine is ignorant of.
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12. Centralized healthcare's ignorance of the basics of this Tweet thread has led to incalculable errors for public health. I mentioned this to @RickRubin & @hubermanlab when we spoke about Dr. Changs' belief it made 50% of what is in the textbooks obsolete. I am telling you 99.9% is hot garbage. Why? The number one opsin in mammals is MELANOPSIN and we no longer live under the sun. We live inside under LED light that destroys this non-visual photoreceptive circuit. People want to blame glucose and insulin yet, when you look at your blood you see this. Does Nature make mistakes or has centralized medicine ignored a lot of facts they should have been asking questions about? When deuterium is let into the matrix this is what redox shift all biochemical pathways the longevity experts THINK never change. This is why none of them understand mTOR and UCP-2. Those proteins embedded in the lipid rafts or connected to them by the tensegrity system change how they respond. Why does NO fall as we age? Because modern humans live under an alien light. Why do Apo proteins and LpA look like a problem to the PEter Attias of the world? Because none of his patients in NYC or San Diego live in sunlight. If they did their LDL cholesterol would be low and their HDL would be high and he would not write a new book telling everyone to take a statin because it is a GOOD plan for longevity. This message is DEAD WRONG.
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13. Because ideas like his are allowed to be considered expert opinion, that is why this information has been kept int he shadows by big pharma and big food. I promise you this is why all of you do not know it either. Cholesterol is another nonvisual photoreceptor of man that absorbs best in the UV range. When it is sulfated it's absorption spectra is in the 190-350nm range. When it's in its LDL it absorbs at 500-600nm (winter/blue light). For example, if you have the wrong type of cholesterol in your skin when the sun is strong you won't be able to make Vitamin D at all even at the equator. This explains why people who live indoors and work in offices all have high cholesterol. It also means they are all collecting deuterium in their systems instead of H+. Since your mito matric runs purely on H+ you might see the problem now why heart brain and PAD diseases are all linked. Cholesterol has to be sulfated and in the HDL format because those electrons are needed to absorb the 290-320 nm light. THIS IS THE REDUCED VERSION OF CHOLESTEROL mammals use in spring and summer. If your HDL is low it is because you LIVE MOSTLY IN BLUE LIGHT or nnEMF stress. REMEMBER LIGHT ONLY WORKS WITH ELECTRONS. LDL cholesterol is DEVOID of electrons and sulfur. when you have the wrong type of cholesterol in your skin, the lipid rafts change the voltage gate channel operation of proteins embedded in them to alter function to match the light. When the system is disordered, as it is in most people in California/NYC due to blue light and nnEMF, not even standing on the equator naked will raise your vitamin D level. It is Biophysics 101. Right now this is why people in California and NYC have record rates of LDL cholesterol levels, low vitamin D levels, metabolic syndrome in the liver, and higher rates of skin cancer, colon cancer, and melasma. It is fully explainable when you get how light controls mammals. Keep enjoying your tech and NYC/Cali and prep for a life filled with problems that centralized scheme will wallet biopsy with regularity.
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14. I mentioned metabolic syndrome and liver disease. My new young protege, @MaxGulhaneMD is very concerned about fatty liver and is convinced that seed oils are behind it as most of the meat heads in carnivores seen are. Time to educate them. https://t.co/4mFWrPrCVv
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15. There is strong class one evidence of a significant relation of 25(OH)D levels with the degree of liver dysfunction, considering that an inverse correlation of 25(OH)D levels with both Child-Pugh score and Model for End-Stage Liver Disease has been reported in the GI literature. In addition, vitamin D deficiency has been shown to increase the risk for overall mortality and infections in patients with cirrhosis. Vitamin D deficiency has been also associated with advanced stages of hepatocellular carcinoma and poor prognosis. Finally, there are studies suggesting that patients with chronic hepatitis C and normal vitamin D levels have higher virological responses to treatment. The sun is always the answer for liver disease = decentralized wisdom 101. It is not the meat diet. That solution is 4 steps below the sun.
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16. #1 is sunlight ALWAYS. This is why Vitamin D is converted into an active neurohormone in the body. Key proxies to look at for decentralized clinicians = look at blood glucose, LDL cholesterol levels, B12, and any surface skin or colon color changes (endoscopy). If any of them are abnormal your liver is getting pounded and the melanin sheets at the organ of Zuckerkandl are being degraded. Women with melasma and men with melanosis coli you are in trouble and you are collecting deuterium in your liver to grow a fatty liver. Note the date on the paper and ask yourself why is that every time the GI guy sticks the black snake in my rectum he has never told me this if the data is 30 years old? WHY?
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17. the organ of Zuckerlandl is a chromaffin body derived from the neural crest, loaded with melanin sheets that services the liver, intestines, stomach, pancreas, spleen, gallbladder, kidney, and adrenal medulla and is part of the melanin network that is located at the bifurcation of the aorta or at the origin of the inferior mesenteric artery. This nonvisual photoreceptive array connects with the enterochromaffin cells of the gut that contain massive stores of melanin and aromatic amino acids in the lumen of the gut and in the intestinal wall. Tryptophan is the key time crystal in the gut and the sympathetic nervous system allowing mammals to know precisely where the Earth is in relation to the sun during a revolution cycle on Earth. I wrote a blog on how that works on Patreon. Read it. This allows for the perfect planetary adaptation of the organism to change its skin and gut biology to absorb solar light PROPERLY.
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18. This directs the turnover of enterocytes to a 24-48 cycle designed to remove deuterium from the blood and lumen so the liver does not get fatty. This same organ of Zuckerlandl controls your adrenal medulla on the top of your kidney. The POMC gene cleavage releases ACTH. This ACTH allows for high-flux mitochondrial cholesterol trafficking in tissues where POMC is located in post-mitotic cells in adult mammals. It turns out that in the heavily melanated adrenal cortex, this is a specialized function in the mammalian clade. Chromaffin cells migrate to the area adjacent to the sympathetic ganglia with neural crest-derived POMC neurons via the somites migration plan to the adrenal medulla where they're the most abundant type of cells in mammals. The largest extra-adrenal cluster of chromaffin cells in mammals is the organ of Zuckerkandl. Sunlight expands this organ and the adrenal medulla to improve liver and kidney functioning. This is skin 25 D(OH) is converted in both organs to the active format of D3. That vitamin D3 then binds to the VDR in the matrix to slow ECT to stop the need for food to run the ATPase. The 43% of red light in the solar spectrum can spin the ATPase and the liver becomes protected from the deuterium loads. If the load gets in because of bad mammalian ideas, the enterocytes can still slough off every day to protect the liver if the SCN clock is operational because the mammal is in the sun getting UV light. The 380 nm light hitting the RPE informs mTOR to be in its catabolic or anabolic state = which controls the flow of protons into mitochondria in the liver. That is the circle of control of the liver. NOTHING is better for liver diseases than the sun.
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19. THE END OF THE LESSON https://t.co/AZ1qHB0w9k
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1. Today's lesson is on TBI. I am just finishing a hellish week of trauma call and since I saw at least ten of these in the last 7 days lets discuss them.
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2. What are the effects of the neurometabolic consequences of concussions = hypothalamic-pituitary damage that leads to = protein folding issues in cells due to lowered redox = CTE = poor cognitive ability? The shock wave the CSF experiences in brain trauma also chains the hydrogen bonding network in CSF to alter the density of the water in CSF adjacent to the brain's neocortex.
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3. This shock wave makes CSF less dense, and when CSF is less dense, the laws of physics control information transfer in water, decreasing it, leading to poor neurologic function and poor cognition. This change on the surface of the brain alters neurons at deeper levels in our brain. THE TTFL (QE #55 on PAtreon) IS ALSO ALTERED BECAUSE OF THE SHOCK WAVE, and this is why TBI IS ALWAYS associated with circadian symptoms.
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4. When inflammation is present in the brain, the three fundamental laws of nature are altered. 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. This single event uncouples mitochondrion in the neocortex, and it raises that neuron’s basal metabolic rate.
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5. This increases the cerebral blood flow because the brain's electric circuitry goes awry. This mimics the original CAT SCAN machine experiment he did/built because the injury created to slaughter cows used electric current, which raised the cow's cerebral blood flow and rendered the images useless.
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6. 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 precisely how leptin resistance causes (obesity and) a neuro-cognitive decline in humans. The CSF around the hypothalamus becomes less dense, looses melanin in the leptin melanocortin pathway and has a higher temperature with higher levels of cytokines in it, causing us to lose energy/info to the environment.
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7. This increase in CBF, in turn, decreases CSF creation, lowering glymphatic drainage in the brain, and more toxins collect over time and give the symptoms of a TBI as it gets worse from the injury. It also raises your blood presure. This injury mechanism is radically different from other parts of the body because of how the brain anatomy differs from other organs.
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8. We’ve known for a long time that only two things lower the metabolic rate in living things: strong solar stimulus and cooling. The problem for CENTRALIZED medicine is that these scaling laws (Kleiber's law) of energy flux have not yet made it into clinical medicine. 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 = decentralized medicine 101. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC155411/
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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. https://jackkruse.com/emf-2-einstein-meet-leptin/
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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.
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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.
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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.
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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.
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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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1. Sunlight releases 250-780 nm light. 250-270 nm light is UVC light. Anything below this level is considered VUV light. The UV-C and VUV light is the light that scares physicians for only one reason. Big Pharma has convinced them that this causes direct DNA damage to human cells so it needs to be eliminated. I wonder what will happen when we build a photomultiplier that can measure the spectrum emitted from cells and find out that we create both UVC and VUV light? IS THIS Big Pharma MEME TRUE about the toxicity of deep UV light? No, it is not. Why does it persist? Once humans harness the sun's frequencies in this area we won't have a lot of drugs in healthcare to treat a lot of diseases. The sun's light is a decentralized compound pharmacy for health. @RickRubin This belief/perception is why light confusion exists and few studies are being done in vivo. Be aware of this. In summary, it has been known during the past one hundred years that UVC irradiation is highly bactericidal; however, using UVC illumination for the prevention and treatment of localized infections is still in the very early stages of development because of the influence of Big Pharma's profiteering. @hubermanlab Most of the studies are limited to in vitro and ex vivo levels, while in vivo animal studies and clinical studies are much rarer. A major advantage of using UVC over antibiotics is that UVC can rapidly eradicate resistant and pathogenic microorganisms without any systemic side effects. UVC may also be much more cost-effective than the commonly used antibiotics. SHOCKER to no one except the centralized shills. @JuicefBukele https://ncbi.nlm.nih.gov/pmc/articles/PMC3831650/
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2. Centralized medicine born from Rockefeller has some good points, and is great in an acute emergency situation, but it’s high time people realized that today’s mainstream medicine (Western centralized medicine or allopathy or functional medicine), with its focus on drug supplements, drugs, radiation, drugs, surgery, drugs and more drugs, is at its foundation a money-spinning Rockefeller creation.
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3. This thread will detail the bizarre history behind John D. Rockefeller's creation of centralized Big Pharma and the foundations of Western Medicine that are destroying our metabolic health. @JuicefBukele John D. Rockefeller was an oil magnate and one of the richest men in history. He was America’s first billionaire and amassed a fortune of $498B adjusted for inflation of the USD as of 2023.
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@JuicefBukele 4. Through monopolistic practices, Rockefeller grew his company, Standard Oil, to control 90% of all oil refineries in the U.S. Standard Oil has since broken up and has now become Chevron, Exxon, Mobil, etc. Yes, that’s how big Standard Oil was in its prime.
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5. In 1900, Scientists discovered petrochemicals. These were chemicals that could be created from oil. Bakelite, the first plastic, was created from oil in 1907. Scientists were discovering various synthetic vitamins that could be used to treat illnesses such as Scurvy and Rickets that were caused by Vitamin deficiencies. Rockefeller thought that Petrochemicals could also be used to create vitamins and medications. Petrochemicals would allow Rockefeller to monopolize another industry in addition to oil. Business-wise, Rockefeller could patent these Petrochemicals and sell them for immense profits. Rockefeller acted quickly and purchased part of I.G. Farben - a German manufacturing company. Side Note: I.G. Farben supplied the Nazis during WWII. Yep, look it up. However, Rockefeller faced a major dilemma as he looked to monopolize medicine: Natural and herbal medicines were incredibly popular at the time due to the vitalists in medicine who were practicing the first version of decentralized medicine at the time. Many doctors and medical schools in the US were advocating practices born in NATURE as treatment & cures. Like he did for other competing oil companies, Rockefeller viewed natural remedies as his "competition" that needed to be decimated. Rockefeller teamed up with Andrew Carnegie and hired a man named Abraham Flexner through the Carnegie Foundation to do just that. He decided to control the curriculum of all US medical schools to change the narrative with propaganda.
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@JuicefBukele Flexner’s role was to travel the US and review Medical schools & hospitals across the country. This led to the Flexner Report which resulted in the closure of almost 50% of all medical schools.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist 🟩🔆
7. Natural medicines, uses of electric and magnetic currents, and chiropractic care, were utterly decimated in the report. Some holistic doctors were even jailed. Rockefeller also donated a whopping $100M to colleges and hospitals under his philanthropic group called the General Education Board. Flexner's report got us away from bioelectricity and toward the biochemical pathway before the discovery of DNA in 1953. This is when centralized medicine became an NGO of the Rockefeller foundation to ruin the health of North America. This was payback to Teddy Roosevelt. The goal was to bankrupt the US by creating a paradigm of sickness. Every American was now viewed as a customer in sick care. If you cured them the Rockefeller Foundation lost money through their Big Pharma subsidiaries. This is how Harvard, the Mayo Clinic, & Johns Hopkins came to dominate modern centralized medicine and policy. Nothing in this paradigm is evidence-based when you control the curriculum being TAUGHT and the research that gets funded and published as we saw in the pandemic era. The DNA discovery entrenched us in the Rockefeller paradigm of drugs over Nature. In a short period of time, medical schools & hospitals were homogenized with the same approach. Their curricula became the first algorithm used in medicine to suit a profiteer. Medicine was just about patented drugs, not utilizing holistic & natural approaches as treatment. Rockefeller's next step was to launch a smear campaign against his holistic "competitors." Homeopathy and Natural Medicines were quickly discredited by the newspapers and media outlets. He used the media as his propaganda machine to create Big Pharma.
@DrJackKruse - ☣️ Pleb Kruse = BTC foundationalist 🟩🔆
8. Rockefeller's approach worked incredibly well as he decimated the decentralized competition in healthcare and ultimately created our current centralized medical system. This system continues today: Big Pharma makes large donations to medical schools in exchange for these schools to prescribe their drugs. They also buy most of the ads on media and these are their current marketing arms to push narratives they want pushed into your consciousness. This is why people think these tertiary care centers of excellent are good places........... They are sausage factories for patients' tissues and lives. Again, this post is not to bash Western centralized Medicine. It is to spread SUNSHINE on show the unfiltered history of John D. Rockefeller and the role he played in shaping our current centralized healthcare system.
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9. The next time your CENTRALIZED doctor spends 3 minutes with you during your visit and you feel like a "customer" instead of a patient and you get handed an Rx for all your ills and complaints, this post will hopefully give you clarity on why it is happening. Not surprisingly, the cost of medical care in the US is #1 in the world, yet our quality is ranked at #37. Yet, some people I have recently met thought that following the Tertiary care centers pathways in healthcare were WISE? Some bridges need to be burned down so we never go down them again.
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10. It is your responsibility to be the DECENTRALIZED CEO of your own health. At the end of the day, no one cares about your own health more than you. Take in a variety of different inputs and make the decision of what is in your best interest. Food is the fuel of the mitochondrial engines. The Mitochondrial engines are quantum photomultipliers of food's electromagnetic bar code built by the sun and Earth's environments. Food changes as the sun varies and the environment on Earth changes. Start seeing the sun and Earth's environment that determine how your engines operate. Start seeing your food and lifestyle as a version of decentralized medicine. Be intentional about where you source your food and the amount of sun and darkness at night you get to improve the sleep you get. Use these as your pillars to THRIVE. Just how good has the Mayo Clinic been for the Public Health The ROI of centralized medicine in one chart.
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11. Never Forget it was the Mayo Clinic, Harvard, and Johns Hopkins led the charge to this demise over the last three years. Remember what the mandate was pushing and who created it. Aftermarket data: A great deal of intelligence has been invested in the ignorance of modern centralized healthcare. We can now see that in the mRNA experiment done globally over the last two years. The Morbidity and Mortality conference of the actions of the players should get them all fired and thrown in jail.
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12. Future centralized doctors are ill-prepared for a world of patients bathing in nnEMF that changes how organic chemistry operates in cells. Hire decentralized docs who aced organic chemistry and every other type of chemistry associated with the biophysics of life. I wonder if med school admissions departments will get the names of the premed students who signed this petition? It seems like an important piece of info when considering their fitness for medicine, no?https://www.nytimes.com/2022/10/03/us/nyu-organic-chemistry-petition.html
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13. This is how centralized medicine PEER review is done, folks. If you can get a study to support your drug... you publish it. If the trial failed you disregard it. It's called publication bias. It sits at the deceit of the centralized system of medicine. When you consider the totality of the scientific evidence you quickly discover antidepressants are a placebo with horrible side effects & potential for serious adverse consequences. Unfortunately, most doctors are not even aware of this and with Google patrolling and changing how search is done, any non-suspecting person will just do a quick Google search & read a biased study claiming this drug works. Always question Big Pharma's claim of evidence.
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14. In a very short time, Rockefeller obtained his goal of paying back the US gov't for breaking up his Oil empire. Medical colleges at the time were all streamlined and homogenized. All the students were learning the same thing, and medicine was all about using patented drugs from his new companies spun off in NJ from Standard Oil. CENTRALIZED Scientists received huge grants to study how plants cured diseases, but their goal was to first identify which chemicals in the plant were effective, and then recreate a similar chemical – but not identical – in the lab that could be patented. This is how the shill PhD was born. A pill for the ill became the mantra of modern centralized medicine. No one has wrecked more damage to the public health than the Rockefeller Foundation. So, now we are, 100 years later, churning out centralized doctors who know nothing about the benefits of nutrition or herbs or any Natural practices around light water and magnetism and mitochondrial DNA. We have an entire society that is enslaved to corporations for its well-being. America spends 15% of its GDP on healthcare, which should be really called “sick care.” It is focused not on cure, but only on symptoms, thus creating repeat customers. There is no cure for cancer, diabetes, autism, asthma, or even flu. Why would there be real cures? This is a system founded by oligarchs and plutocrats, not by doctors.
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15. I'd heard a reference to sunlight containing Lithium via a song by Sting .... "Lithium Sunset" When asked about the sun he said..... “The idea for this song came to me when I was in Brazil, I have a great fondness for Brazil, and I met what I can best describe as a shaman (who happens to have a degree in Chemistry). He was explaining something to me, he was saying that sunlight is composed of a lot of elements and one of them is Lithium, as you know, Lithium is a medication given to the depressed, it’s a very successful drug. But it actually exists in sunlight and at sunrise and sunset you can look into the sun without damage the eye does not filter yellow light so the Lithium goes straight to the brain. This is why people get a great deal of comfort and solace from looking at the sunset or the sunrise. So I wrote a song called “Lithium Sunset” which is an ode to this natural medication that is available to all.” Sting (422) How can light contain Lithium doc ....? This doesn't make sense. Dr. Kruse responds: Don all elements on the periodic table have a specific light frequency they emit and this is their light fingerprint. This fingerprint can travel 93 million miles to Earth to interact with chemicals that contain this element and it will react to this similar frequency via a vibration. We call this molecular resonance. I have written extensively about it in the blog and on my forum. You need to understand how this light fingerprint can be used to activate Lithium in your brain to change your mood. That is how all elements and all bio-molecules work. We've been conditioned to believe it is a lock and key mechanism but this is a very simplistic linear way of thinking about chemistry. Light controls all chemicals by imparting information and energy to their valence electrons and once the light frequency matches the element or chemical the distant element or chemical reacts. This is how sunlight can affect a depressed brain. It turns out lithium light from the sun is more abundant in AM and sunset light so Sting was right about his song. In fact, he used this to stimulate his own creativity when he had writer's block in his career. So let me give you some deep basics about how this works in you......... Human skin's optical window is tight and is between 500nm -1000nm. 42 %-49% of sunlight is IR-A light. IR-A light has a wavelength of 0.75–1.4 µm IR-A frequencies range is 214–400 THz The electron volts of IR-A is 886–1653 meV and its temperature range is 3,864–2,070 K (3,591–1,797 °C) The human eye cannot see it but these frequencies are present all the time when sunlight is present and this light innovates quantum solutions for living things. Each chemical bond in a molecule vibrates at a frequency characteristic of that bond. A group of atoms in a molecule (e.g., CH2) may have multiple modes of oscillation caused by the stretching and bending motions of the group as a whole. If an oscillation leads to a change in dipole in the molecule then it will absorb a photon that has the same frequency. The vibrational frequencies of most molecules correspond to the frequencies of infrared light. Infrared radiation is emitted or absorbed by molecules when they change their rotational-vibrational movements. It excites vibrational modes in a molecule through a change in the dipole moment, making it a useful frequency range for the study of these energy states for molecules of the proper symmetry. When hormones are altered so they can be patented these small changes alter their dipole moment and change chemistry in some small way but can have huge implications when this chemical interacts with light via the optical window of the skin. When you know better........you do better. This is DECENTRALAIZED MEDICINE.
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16. When your melatonin/cortisol rhythm is off due to dark indoor days and bright artificially lit nights, not only are you affecting sleep and hormone levels, but you are also changing the size and shape of your mitochondria which changes your magnesium levels in the matrix and its hydration shell. This leads to energy inefficiency and age/disease acceleration. Did you know the size and shape of your hydration shell of magnesium is the ion lever that red light from the sun works on to change energy dynamics in the mitochondrial matrix? This is DECENTRALIZED MEDICINE. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284776/
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17. We know that there are several exceptions in the standard genetic code for codons but over the 3.8 billion years of evolution, there is only one codon as methionine code for tryptophan. That is an extraordinary fact. It is as extraordinary as DHA never being replaced in 600 million years of eukaryotic evolution in the nervous system and in cell membranes. It is so extraordinary that there must be a missing role in biology that has yet to be discovered about why this is true. This blog is about that reason. THIS IS DECENTRALIZED MEDICINE. https://www.patreon.com/posts/19082581
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18. So you might be wondering if DHA is so critical to humans how did it show up on Earth initially? Before DHA, Molybdenum was the key element for bacteria and archaea that used the sun for energy. The clocks in us measure and control the flow of entropy in us. The time stamping of light and dark on post-translational DNA by the mt DNA is how DECENTRALIZED MEDICINE WORKS. It is time you all wake up and stop supporting the criminals who created centralized healthcare. https://www.patreon.com/posts/55049793
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19. THE LESSON IS OVER. REJECT CENTRALIZED IDEAS IN HEALTHCARE. Most of them are bad for you and good for the progeny of Rockefeller's plan. https://t.co/HKOSgLwkff