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.Image
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.
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.
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
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.
6. Now about that superior cervical ganglion and how it links to the blue light non visual photoreceptor, melanopsin.......... Image
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.
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?

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?
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.


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.
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.



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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.
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.
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.
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.
17. Oh and if you think there is not good data on that vagus nerve water connection............psychologytoday.com/intl/blog/the-…
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.
19. Light controls the two decentrlaized networks in the world.........never forget it. See above pic for reenforcement. Image
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.
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 Image

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More from @DrJackKruse

Feb 19
For those of you who don't know glyphsate toxicity is related to it being a competive inhibitor to melanin and when melanin is destroyed in your eye the RPE-SCN complex is destroyed and this is what leads to chronic disease creation, disability, and short longevity.

In evolution of mammals from amphibians 320 million yrs ago, the post-aquatic transition, mammals internalized photonic signaling via RPE-SCN-RHT tracts, where RPE melanin transduces light into UPEs, effectively relaying endogenous light to the SCN to gain high fidelity circadian/seasonal signaling.

Implications? Mammalian Complexity Management was built around Chromosome #2. This really changed in primates 7-9 million yrs ago when we had a fusion event that allowed primate germ lines to go from 24 pairs to 23 pairs in humans. This fusion event put a strong optical battery in between the new human chromosome. This telomeric fusion allows endogenous UPEs stronger than terrestrial light to become a possibility and this is why human primates are born with so much Sub Q fat and primates are born with none.

The physics of terrestrial light had a lesson for us most missed except for Rockefeller medicine who realized initiall what this meant because of the development of glyphosate on melanin in the Green Revolution of the 1950-1975. Leptin's absorption peak at ~220 nm (UVC, peptide bond-driven) is absent in terrestrial sunlight, implying that the human eye had to have a reliance on endogenous UPE from mitochondrial ROS from the RPE to make it happen. This was the biggest signal for me in 2005 linking my Quilt thesis to what happened in MKULTRA in the Charity Hospital boxes. Why? It told me the story of light in mammals was linked to endogenous control of the SCN via melanin in the eye.

You'd be wise to look at the skin where melanin is embedded in cholestrol and know the following: Leptin's 220 nm EXACTLY sensitivity matches cholesterol's (another non-visual photoreceptor) absorption spectra, enabling quantum coherence in neural/mitochondrial networks for INTERNAL "space-time" control, optimizing entropy dissipation in complex systems. HOW?

Neuroendocrine healing = POMC biology on Chromosome 2.

Summary of the Feedback Loop MAHA KEEPs MISSING because Wiles has made them MIGA Rockefeller compliant via MAHA.

Early Light Stress from global MKULTRA collateral effects

Methylates POMC

Blunts HPA axis and alpha -MSH
Blue Light

Damages Melanopsin

Desynchronizes Mitochondria and Melatonin.
Hypomyelination

Allows "noise" to dictate Synaptic Pruning

Semi-Permanent neural miswiring
Matrix Collapse ----> Motochondrial ROS -----> developing metabolic syndrome in brain & Atrophic Skin = Syd Barrett phenotype where you become comfortably numb in your current NOW. This is why everyone is apathetic and nihilistic. Not everyone in the world will exhibit the same stress because two in your family are UNMYELINATED when it comes to light.

So then Rockefeller Dynasty came up with the briallint idea to spike foods and farming with another competive inhibitor of melanin called glyposate in 1975 and unleash it.

Humanity's Low Vitamin D issue in a nut shell:

It isn't a permanent genetic curse, but rather a state of extreme thermodynamic debt in your skin that has to be repaid to get well. Your skin controls trillions of matrix on the inside of your body using melanin ability to chelate all the matirx cofator metals = Fe, Cu, Mn, Mo, Zn, Ca, and deuterium. Mitochondria are not just static "power plants"; they function as a networked colony using the biophysics of metal chelation.

The SKIN and Gut is a Signaling Vacuum in our humanity family: In early to late-stage POMC burnout due to nnEMF , patients become marginalized, living in low-light indoor environments (blue light/non-native EMFs) with NOT ENOUGHT exposure to UV-A/B or seasonal temperature shifts to repay the debt they accumulated in the past. The defects in the brain mitochondria from the debt does not allow them to understand the linkage fully.

The etiology I am describing here is an interplay of what a light stressed environment early on to an unmyelinated brain causes via silenced POMC, dopamine supersensitivity, and GABA/melatonin desynchrony. Non of the food guru MAHA retards have a clue about the biophysics of mitochondria and that is why DJT gave his Rockefeller BigHarma guys glyphosate immunity. Susie Wiles made it easy as their chief lobbyist and DJT COS.

Now for the retard centalized MDs trained by Rockefeller curriculums since 1911. The Melanopsin-Optic Chiasm Link (The "Siamese Cat" Effect)
I’ve pinpointed a crucial anatomical parallel in the Quantum Engineering #45 blog on Autism I wrote for Nicole Shannahan. In Siamese cats, a mutation in tyrosinase (linked to melanin destruction by light,nnEMF, glyphosate) causes the optic fibers to misroute at the optic chiasm. In humans it does it in brain = mimics metabolic syndrome brain we see in diabetics.

Melanopsin & Circuitry: Melanopsin-containing retinal ganglion cells (ipRGCs) are the "master clocks." Blue light toxicity (HEV light) damages these cells, sending a "distorted signal" to the Suprachiasmatic Nucleus (SCN).

Axonal Guidance: If the light signal is incoherent during the childhood "window of hypomyelination," the axonal guidance molecules (which are often regulated by POMC derivatives) fail to route correctly. The result is a "functional" miswiring of the brain & skin in the kids, similar to the Siamese cat's visual system, where sensory input and internal processing are fundamentally decoupled.

The Mitochondrial Matrix & Metabolic Syndrome
You should begin to get some intuition about why atrophic skin and the mitochondrial matrix LINK is deeply supported by the "Skin-Brain-Endocrine" axis:

Skin as a Solar Panel: The skin is a major site of POMC expression. Reduced POMC leads to thinning (atrophy) and reduced melanin. Melanin is not just a pigment; it is an energy transducer that protects the mitochondrial matrix from oxidative "overheating." How, you ask?

UV light from the sun transcribes melanin. Melanin then absorbs tons of light for you. What else does UV light do? It makes Nitric oxide and Vitamin D. What do both of them do? They inhibit energy production in the matrix,

NO inhibits CCO. What does Vitamin D do to the VDR on the IMM? It slows ETC. Nature built you to never overheat in the sun filled with UV light, Rockefeller curriculums taught you the opposite and demonized the sun since 1950. None of the retards in centralized medicine looked carefully enough at the wiring diagram of mitochondria, especially around CCO and the IMM. UV exposure is critical. And UV light translates alpha MSH to make MELANIN.

This tells you there is NO SET POINT for solar exposure EVER except when you have ATROPHIC skin lacking melanin, cholesterol and water from CCO, which most of you do.

What else does POMC also do? It ALSO releases beta-endorphin when you are in UV light which makes us addicted to the sun exposure so these question never come up. If you do not seek the sun it means by definition you have not gotten enough sun to cleave POMC to make beta endorphin.

The real reason you overheat in the sun is likely a defect in your exhaust pipe = eccrine or exocrine system.

Rockefeller medicine destroyed that human mechanism on chromosome 2 in 2005 when they invented Byetta to destory GLP1-GLP2 signaling via the glucagon gene.

Rockefeller trained MDs to be obedient idiots so they are all assisting the genocide going on in COVId, GAZA and BigHarma. That is DJT MAGA now. MIGA MIGA MIGA.

Wake the fuck up savages.

Metabolic Syndrome in many conditions does not look like it does in diabetics but it is also associated with people with poor Vitamin D creation. Without POMC-derived peptides in your skin to regulate the mitochondrial matrix, the mitochondria begin to "leak" protons and produce excessive Reactive Oxygen Species (ROS). This mitochondrial dysfunction is the literal engine of metabolic syndrome brains which struggle with cognition and stacking lessons. It causes the body to shift into a "survival mode" = Warburg metabolism. If it is left untreated for decades the effects will show up in the gut = METABOLIC SYNDROME.

The Neurochemical Cascade (Dopamine, GABA, Melatonin)
When POMC is silenced by stress-induced methylation, it doesn't just affect ACTH; it affects the entire "cleavage tree" of the protein, including a-MSH.

Dopamine & GABA: In the retina and brain with alpha -MSH and dopamine act as counter-balances. Reduced POMC leads to a loss of dopaminergic tone and a failure of GABAergic inhibitory neurons to provide "braking" for neural circuits. Without this inhibition, the "fire together, wire together" (Hebb’s Law) principle goes haywire, leading to the abnormal synaptic pruning and "miswiring" seen in schizophrenia.

Melatonin: Melatonin synthesis is light-dependent and occurs both in the pineal gland and the mitochondrial matrix. If the circadian rhythm is broken by blue light damage to melanopsin, melatonin production fails, stripping the mitochondria of their most potent antioxidant.

The Melanopsin-Optic Chiasm Link (The "Siamese Cat" Effect)
I’ve pinpointed a crucial anatomical parallel in the Quantum Engineering #45 blog on Autism I wrote for Nicole Shannahan. In Siamese cats, a mutation in tyrosinase (linked to melanin) causes the optic fibers to misroute at the optic chiasm.

Melanopsin & Circuitry: Melanopsin-containing retinal ganglion cells (ipRGCs) are the "master clocks." Blue light toxicity (HEV light) damages these cells, sending a "distorted signal" via the RPE to the Suprachiasmatic Nucleus (SCN).

Axonal Guidance: If the light signal is incoherent during the childhood "window of hypomyelination," the axonal guidance molecules (which are often regulated by POMC derivatives) fail to route correctly. The result is a "functional" miswiring of the brain, similar to the Siamese cat's visual system, where sensory input and internal processing are fundamentally decoupled.

They used nnEMF first from MKULTRA to dumb you down then glyphosate was the kill shot.

Glyphosate: The Melanin-Chelation Kill Switch
My insight into glyphosate as a noncompetitive inhibitor of tyrosinase is the "smoking gun" for the modern chronic disease explosion.
The Metal Coup: Melanin is the "Master Chelator." It controls the Cu, Fe, Mn, and Moneeded for mitochondrial health. By inhibiting melanin, glyphosate forces the body to lose its "magnetic grip" on these metals.
The Atavistic Reversion (PaxB): Without melanin to govern the signals in the RPE, the high-resolution mammalian "GPS" (the RPE-SCN-POMC axis) fails.
The tissue defaults to the PaxB primitive blueprint from the GOE, leading to the "mass-accumulation" of many atoms which leads to phenotypes of cancer, obesity, and neurodegeneration thank the banking elite and their BigHarma companies are using to bankrupt America.Image
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2. The 2005 GLP 1 & GLP 2 phase was built by Rockefeller when the discovered leptin in 1994 in NYC at Rockefeller University so those of you who broken as fuck to ask and beg for medically assisted suicide because the retards in centralized medicine and functional medicine are too fucking lazy to read how they did it to you all with your consent. .Image
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3. Room 5600: The Professionalization of Biotech Warfare blue light+glyphosate+GLP1 is the killing fields for BigHarma profits.

J. Richardson Dilworth was the architect of the financial "Pivot." He shifted the Rockefeller "Room 5600" from 19th-century industrialism to 21st-century Biotech Control.

The Venrock Ecosystem: By seeding Amgen and its peers, the family office created a "Multi-Client" trap. They funded the discovery of Leptin (1994) specifically because they already knew from the DARPA MKULTRA program that melanin was the key target to hit in farming. Glyphosate is a competive inhibitor of melanin. Few know it.

The Shelved the Leptin Trials: When the leptin trials showed that Light and Cold were the actual regulators of the pathway, they couldn't commercialize that, because there’s no profit in the Sun. So, they shelved the "Photonic" truth and pivoted to the Distal pathway below photonics and elevated the GLP-1 Agonists to treat the symptoms of the light-starved world they built in the 1960's BigTech revolution in Silicon Valley. Steve Jobs links to Rockefeller and Rothschild is deep.

The connection between Steve Jobs and the Rockefeller and Rothschild families is primarily rooted in
early-stage venture capital, shared high-level board memberships, and modern institutional investment. While Jobs was an adopted child of a working-class couple, his career in Silicon Valley was deeply intertwined with the financial infrastructure established by these dynasties.

The Rockefeller family’s venture capital arm, Venrock Associates, was one of the early investors in Apple Computer during its start-up phase in Silicon Valley. This initial capital was crucial for transitioning Apple from a hobbyist project into a scalable corporation. Venrock's involvement established a direct link between the Rockefeller family office (established in 1882) and the nascent personal computing industry.
The Rothschild family has maintained a significant financial interest in Apple through various investment vehicles:Rothschild Investment Corp: This firm identifies Apple Inc. (AAPL) as one of its top holdings in recent SEC filings.

RIT Capital Partners: Chaired by Lord Jacob Rothschild, this London-listed trust acquired a 37% stake in Rockefeller Financial Services in 2012, formally uniting the two dynasties' wealth management interests.

Laurene Powell Jobs, Steve Jobs’ widow, serves as a bridge to the elite policy circles traditionally associated with the Rockefellers:Council on Foreign Relations (CFR): Laurene Powell Jobs serves on the board of the CFR, an organization famously chaired by David Rockefeller from 1970 to 1985.
Ford Foundation: She also sits on the board of the Ford Foundation, another pillar of the philanthropic network where the Rockefeller influence is historically substantial

Jobs is often compared to John D. Rockefeller in terms of his business impact. While Rockefeller revolutionized industry through vertical integration, Jobs transformed technology through a closed ecosystem that redefined global consumer behavior = Why the Epstein emails call Jobs brilliant. Jobs and John D. Rockefeller integrated their business just like Groves did in the Manhattan Project. Go re listen to my Podcast with Breedlove on Groves.

All tied to my banned Ted talk, FYI.Image
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Read 4 tweets
Feb 16
@MaxGulhaneMD I do have to say after the first 20 minutes I like the discussion but I was frustrated in spots where he was physics facile as he could have been but it is clear Nunn believes as I do that biology is not fundamental it is biophysical.

He is too much in love with Levin. Levin has do nothing to advance Becker.

But I want to tell you at the 1:10 mark you bring up CCO and DDW. Nunn seems uncomfortable.

He goes on to talk KIE boilerplate but he is a biochemist and is dabbling in biphysics so you need to push and extend him further on the D/H+ isotope selection process tied to photosynethesis creation of deuterium on the carbon backbone. there has to be a way to sort the isoptopes and there is biophysically but I do not think he knows what it is.

DDW, heat, and UPEs are exhaust products from matrix operation. He seems to know this. But so is CO2. He does not seem to know the biophysics of CO2 and its real purpose.

The Failure of Centralized "Exhaust" Logic is always on display with Nunn here.
Centralized medicine tries to "fix" CO₂ levels or pH chemically, failing to realize they are tweaking the isotopic selection process that uses magnetic tuning of a quantum circuit.

High CO₂ isn't just "acidosis"; it is the cell trying to increase its "Hash Power" and protect its internal water from the "Double-Spend" attack of entropy I describe in my thesis. CO2 is dimagnetic. this means it shields CCO from the magentic fields of the matrix. Ask yourself why? The answer is simple biophysics. It guarantees that H+ is pushed into the intermembrane space so the ATPase has it to use to spin the Fo head. Deuterium has a different magnetic moment so CO2 acts to sort it and keep it away from the Intermembrane space so that the nanotorque engine is not slowed or destroyed. Neither, Nunn, Boros or Somylai know this because they are blinded by biochemical BS.

So because you asked the question he could not answer he is the answer:

The Physics: CO₂ is highly diamagnetic. By concentrating it at the site of water creation (CCO), the cell creates a FOCAL magnetic "quiet zone."

The DC Current: This allows the protons (H+ not D) to flow in a coherent DC current of repair without being scattered by the "vibrational noise" of the environment.

The VDR Link to the shied: The VDR sitting on the IMM acts as the sensor that ensures the CO₂/O₂/Light ratio is tuned to keep this magnetic "shield" active.

VDR: The Photonic Antenna that directs electron flow, speed, and tunneling efficiency before cytochrome C

Fe-S/CCO: The Quantum Engine is the engine that allows electron and proton tunneling

Carbonic Anhydrase in the matrix/CO₂: The Magnetic Shield/Tuner selects the stochiomtery H+ inside the intermembrane space to deliver to the ATPase.
This mechanism is sorting engines into "good/health/CCO and bad/Disease/Cardiolipin/heteroplasmy to get rid of the bad via Cardiolipin, or to extend life with DDW from CCO to hydrate all our semiconductive proteins. Timing from the OUTSIDE environment photonic signals controls this process max. Recall how Vitamin D, Melanin, DDW, NO, and CO2 are all made. Outside in, not inside out. Biochemists always have the inside out framework because this is where biochemistry occurs. Outside in is where biophysics of life begins.

The Calcium-Melanin Nexus: Macro vs. Micro Control
My thesis identification of melanin's macroscopic chelation vs. Vitamin D’s stochastic sorting provides a complete picture of cellular calcium management:

Melanin (The Macro-Buffer): Melanin acts as a high-capacity reservoir that absorbs and stores calcium. Certain light frequencies allow its release. Vitamin D made from 312-320 nm exogenous light on cholesterol esters is sent inside to the kidney and liver for final processing. This binds the VDR on the IMM and it is the VDR that can get into the nucleus to alter it way after the photonics of this axis acts first with clock genes.

This "macroscopic chelation" of melanin provides a stabilizing background, preventing the "vibrational noise" of the environment from immediately overwhelming the cell's delicate electric circuits.

Vitamin D/VDR (The Stochastic Sorter): Sitting on the Inner Mitochondrial Membrane (IMM), the VDR acts as the "fine-tooth comb." It performs stochastic sorting, precisely directing individual Ca²⁺ ions to the TCA cycle dehydrogenases to tune the "Hash Power" (metabolic flux) based on the UVB/IR signals received from the exterior. VDR binding isolates CCO with CL.

The 30 Million Volt Charge: This charge on the IMM is the physical manifestation of the DC current of repair. It encodes photonic information as a voltage gradient, allowing the matrix to "read" the external environment through the language of electron and proton tunneling.Image
2. Other point @MaxGulhaneMD more for you than him. He does not seem to understand an additional neutron = more mass and as mass goes up what does Ilya theory from his Nobel in 1977 say? Timing slows.

So any additional mass irrespecitve of a KIE means that heteroplasmy expands because in CCO you have the story of life and death. A lot of H+ = CCO makes water and CO2.

Too much D+ and it stimulates Cardiolipin. Boros keeps confusing you with broken engines. They do not break. D+ cannot fit in the channel. The ATPase starves and the matrix swells and this stimulates forced apoptosis.

Decentralized Internal light Medicine done by the non visual photoreceptors is "Tuning the Shield"
The VDR, the Fe-S clusters, and the Carbonic Anhydrase system form a Triad of Temporal Control distally to the RPE-SCN.

The CO₂ Diamagnetic Shield
In my model, CO₂ provides the low-entropy environment required for the Protonic Spin-Ice (EZ water) to form. If you look at proton tunneling it is best modelled in ice. What these biochemistry guy don't yet relaize is when melanin is hydrated by DDW you create massive proton tunneling and you open more of the biophysics Pandora box like Grotthaus etcs........Image
3. The Solar vs. nnEMF Split: "Quantized" ROS
My slide below highlights the critical difference in how the cell processes Solar EMF vs. nnEMF (5G/Malware):

Solar EMF (Quantized Information): Sunlight creates a highly specific and sensitive amount of Reactive Oxygen Species (ROS). This is not "damage"; it is quantized information delivered via UVA/Blue light-stimulated Nitric Oxide (NO).

The NO Filter: UVA light controls NO production, which reversibly inhibits Cytochrome c Oxidase (CCO). This acts as a frequency filter for the DC current, preventing the "Double-Spend" entropy attack.

nnEMF Malware (Non-Quantized Noise): Unlike the sun, 5G/nnEMF acts as a Voltage-Gated Calcium Channel (VGCC) disruptor. This causes a massive, non-quantized "leak" of Ca²⁺, leading to:Hydroxyl Radical Flood: The resulting Fenton chemistry creates Hydroxyl Radicals (the most destructive ROS).

Photoreceptor Destruction: This noise "blinds" the internal lighting system of the non visual photoreceptors, leading to mitophagy failure and broken apoptosis, leaving behind a "static colony of defective mitochondria" (the hallmark of chronic disease/cancer).Image
Read 9 tweets
Feb 15
Sorry @MaxGulhaneMD but I chuckled so hard listening to th first 20 minutes of this. When is this guy going to realize that Dr. Pirogine theory on dissipative structures has at its core a TIME SYMMETRY aspect. He still does not get it. Even at the Guy foundation they fly blind.

At life's genesis because of dissipative theory energy was always a commodity, but Time is the real value. He has no idea about the implications of this.

Evolution of life happens because life costly in time, not in energy because of the equations link to entropy.

this idea scales from stars to cells. A supernova has massive energy flux, but it is a state of total chaos (High Entropy). A human brain has much lower energy flux but evolved to have massive Temporal Coherence.

Each "event" in a cell, like a proton tunneling through a molybdenum transistor enzyme in mitochondria or a biophoton hitting a melanin sheet, is a "Block" in the ledger. It’s not "good" or "bad"; it’s a physical State Transition. Wisdom is the ability of the organism to maintain that ledger’s integrity against the "Double-Spend" attack of entropy. Sorry your expert fell short because he is ignorant about the 1977 Nobel Prize implication for mammals.
youtube.com/watch?v=y5DEQ1…
2. Life is costly in time not energy goes right back to the 1977 Noble Prize. At life's genesis chaos has to gain order. Dissipative structure theory really aims to solve this problem for biology by using physics.

Dissipative structure theory led to pioneering research in self-organizing systems, as well as philosophical inquiries into the formation of complexity on biological entities and the quest for a creative and irreversible role of time in the natural sciences.

There is a well-known theorem of minimum entropy production derived by Prigogine, which states that entropy exported from a system reaches a minimum, or becomes zero, at thermodynamic equilibrium and at steady states close to thermodynamic equilibrium. Prigogine's theorem is a direct consequence of Onsager's reciprocity relationship which holds at steady states close to thermodynamic equilibrium. The principle of internal entropy compensation, is in addition to, and implies the principle of minimum entropy production, and may even be valid in regimes far from thermodynamic equilibrium.

He had some very interesting things to say about TIME in his work and Nobel Prize speech. I think they are key to understanding circadian biology and timing. All of our time reversible equations in physics created by Newton, Einstein, and Schrödinger describe a simplification of what actually occurs in nature. We live our lives with eyes blinkered, dismissing reality as the exception to our neatly formed approximations of what time really is.

nobelprize.org/prizes/chemist…
3. Prigogine’s work on Minimum Entropy Production explains why mammals must be "Costly in Time & not in Energy".

By proving that Time is Irreversible, he effectively "Hard Forked" biology away from the time-reversible approximations of Newton and Einstein. Time reversibility is built into the matrix. That is heteroplasmy. As it changes so does time you experience.

Near equilibrium, entropy production is minimized. But life exists far from equilibrium, much to the dismay of all your food guru friends. To maintain complexity, the organism must "export" entropy. This is why life innovated clock genes quick. They are flow meters for entropy.Image
Read 5 tweets
Feb 13
My historical and political analyses have compared
the QAnon phenomena before DJT presidency (45th) and the 1920s Soviet counterintelligence operation "Operation Trust" (Operatsiya Trest) due to their shared use of psychological manipulation to pacify political opposition. If you review my twitter feed you'll see no QAnon posts because I believed they were counter ops of the Zionist controling Israel at this time. Bibi was that leader. He was reaching back into the Zionist bag to the take over of Russia in 1917.

The parallels between these two movements typically center on the following tactics:

"Trust the Plan" Narrative of 4D chess: Both movements relied on the central premise that a secret group of high-ranking insiders, patriots within the government or military, was working covertly to dismantle the regime from within.

Neutralization of Dissent: Operation Trust was designed by the Soviet secret police (Cheka/GPU) to create a fake anti-Bolshevik resistance (the Monarchist Union of Central Russia). Its primary goal was to convince opponents to wait for this "internal coup" rather than taking active measures, effectively stalling real resistance.

Discrediting Opposition: When Operation Trust was exposed in 1927, it humiliated those who had believed in it, making them appear foolish and reducing their willingness to support future anti-Bolshevik efforts.

Luring and Identifying Targets: Just as QAnon encouraged followers to identify themselves online, Operation Trust lured high-profile dissidents like Sidney Reilly and Boris Savinkov back to Russia, where they were captured or executed.

QAnon was part of the plan to turn MAGA to MIGA, in my opinion. The same thing that went on in Russia in 1917 is ongoing in Washington DC.Image
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2. Palantir surveillance will be used to target those who went against this coup and they will be taken care of by the zionist faction that wins this coup between the bankers and transhumanist tech bros. Image
3. Point three as proof of the current coup of America by MIGA:
Read 11 tweets
Feb 12
You missed a big lesson. The "Green Revolution" Pipeline of the 1940-2025 = Melanin Erasure Program

The Rockefeller/Monsanto/Sperry Rand trinity wasn't just about "feeding the world"; it was about standardizing the human bio-frequency.

The Inputs: Rockefeller provided the "seeds," Monsanto provided the "chemical metal-shredder" (Roundup), and Sperry Rand provided the "computational logistics" to scale this melanin-destroying diet globally.

The DARPA Connection: By canceling Robert O. Becker’s lab, DARPA protected this industrial model. They couldn't allow the world to know that we are DC bio-electric organisms whose health depends on the semiconductive fidelity of the melanin that the Green Revolution was designed to erase.
2. Room 5600: The Professionalization of Biotech Warfare

J. Richardson Dilworth was the architect of the financial "Pivot." He shifted the Rockefeller "Room 5600" from 19th-century industrialism to 21st-century Biotech Control.

The Venrock Ecosystem: By seeding Amgen and its peers, the family office created a "Multi-Client" trap. They funded the discovery of Leptin (1994) specifically because they already knew from the DARPA MKULTRA program that melanin was the key target to hit in farming.  Glyphosate is a competive inhibitor of melanin.  Few know it.

The Shelved the Leptin Trials: When the leptin trials showed that Light and Cold were the actual regulators of the pathway, they couldn't commercialize that, because there’s no profit in the Sun. So, they shelved the "Photonic" truth and pivoted to the Distal pathway below photonics and elevated the GLP-1 Agonists to treat the symptoms of the light-starved world they built in the 1960's BigTech revolution in Silicon Valley.  Steve Jobs links to Rockefeller and Rothschild is deep.

The connection between Steve Jobs and the Rockefeller and Rothschild families is primarily rooted inearly-stage venture capital, shared high-level board memberships, and modern institutional investment. While Jobs was an adopted child of a working-class couple, his career in Silicon Valley was deeply intertwined with the financial infrastructure established by these dynasties.

The Rockefeller family’s venture capital arm, Venrock Associates, was one of the early investors in Apple Computer during its start-up phase in Silicon Valley. This initial capital was crucial for transitioning Apple from a hobbyist project into a scalable corporation. Venrock's involvement established a direct link between the Rockefeller family office (established in 1882) and the nascent personal computing industry.

The Rothschild family has maintained a significant financial interest in Apple through various investment vehicles:Rothschild Investment Corp: This firm identifies Apple Inc. (AAPL) as one of its top holdings in recent SEC filings.

RIT Capital Partners: Chaired by Lord Jacob Rothschild, this London-listed trust acquired a 37% stake in Rockefeller Financial Services in 2012, formally uniting the two dynasties' wealth management interests.

Laurene Powell Jobs, Steve Jobs’ widow, serves as a bridge to the elite policy circles traditionally associated with the Rockefellers:Council on Foreign Relations (CFR): Laurene Powell Jobs serves on the board of the CFR, an organization famously chaired by David Rockefeller from 1970 to 1985.

Ford Foundation: She also sits on the board of the Ford Foundation, another pillar of the philanthropic network where the Rockefeller influence is historically substantial

Jobs is often compared to John D. Rockefeller in terms of his business impact. While Rockefeller revolutionized industry through vertical integration, Jobs transformed technology through a closed ecosystem that redefined global consumer behavior = Why the Epstein emails call Jobs brilliant. Jobs and John D. Rockefeller integrated their business just like Groves did in the Manhattan Project. Go re listen to my Podcast with Breedlove on Groves.

Few can rival my research. I am all over these fuckers.Image
3. The Savage's Survival Guide

The "Centralized PhDs" are merely the maintenance crew for the Rockefeller/Amgen/Monsanto grid. They are trained to ignore the RPE-SCN-POMC circuitry because acknowledging it would dismantle the entire $100 million "Leptin Bounty" and the trillion-dollar pharmaceutical "Distal Patch" industry.
Uncle Jack, the warning to the Savages is clear:
Glyphosate is a "Metal Leaking" agent.
Blue Light is a "Timing Shredding agent."
Leptin Resistance is a "Power Outage" signal.
The Monk must not only sell his Ferrari; he must burn the Rockefeller "Roadmap" and reconnect to the DC Bio-Electric Current of the Sun.
How do we begin the "Melanin Reclamation" for the Savages who are currently trapped in the Green Revolution/Agenda 2030 isotopic sink?Image
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Read 5 tweets
Feb 12
Why doesn't Rockefeller centralized medicine work for 99.9% of people?

It is designed to make the family customers not deliver cures for the people.

This is why in Norway right now, below your ability to know it, because zionist media is quiet on it while they feed you Bondi nonsense (circus maximus), they are ransacking the house of the Nobel Committee leader. Jagland. LOL... bastards... Norway the perfect country for corruption.

This is why Epstein was at Harvard and MIT and why Maxwell family controlled PEER review in centralized science. It is why Robert O. Becker was cancelled by the front people (Dr. Phillip Hnadler) for Rockefeller Medicine. The entire scheme was designed to keep Rockefeller medicine in power. Few. Eric Weinstein wants to know why Epstein was in his math dept at MIT. This is why. Control the scientific narratives, control what gets funded and published, control what gets studied and what get buried to Pubsmear (Elisabeth Bik) and then you auction off Nobel Prizes and give them to researchers whose science leads to no cures.

@Kevin_McKernan @JesslovesMJKImage
2. Why doesn't Rockefeller centralized medicine work for 99.9% of people?

It is designed to make the family customers not deliver cures for the people.

This is why in Norway right now, below your ability to know it, because zionist media is quiet on it while they feed you Bondi nonsense (circus maximus),  they are ransacking the house of the Nobel Committee leader. Jagland. LOL... bastards... Norway the perfect country for corruption.

This is why Epstein was at Harvard and MIT and why Maxwell family controlled PEER review in centralized science.  It is why Robert O. Becker was cancelled by the front people (Dr. Phillip Handler) for Rockefeller Medicine.  The entire scheme was designed to keep Rockefeller medicine in power.  Few.  Eric Weinstein wants to know why Epstein was in his math dept at MIT.  This is why.  Control the scientific narratives, control what gets funded and published, control what gets studied and what get buried to Pubsmear (Elisabeth Bik) and then you auction off Nobel Prizes and give them to researchers whose science leads to no cures.  
1.x.com/DrJackKruse/st…  
2.x.com/DissidentMedia…  
3.x.com/DissidentMedia…  
4.x.com/DissidentMedia…
DID YOU READ THE NEW MKULTRA BLOG YET?
patreon.com/posts/cpc-78-n…
3. Are you paying attention Savages? I doubt it.

A new, compact, high-power microwave weapon, the TPG1000Cs, has been developed at a Shanghai Nuclear Technology Institute, which could become one of the most serious threats to the Starlink satellite network.

The device can deliver 20 gigawatts of energy for up to a full minute, the South China Morning Post reported, cited by Portfolio.

The TPG1000Cs, the world’s first compact driver for high-power microwave weapons, has been created at the Northwest Institute of Nuclear Technology in Shanghai. The device can deliver 20 gigawatts of power for up to one minute.

At just four meters long and weighing just five tons, the device is small enough to be mounted on trucks, warships, airplanes, or even satellites. Some Chinese experts estimate that a ground-based microwave weapon with a power of over 1 gigawatt could be capable of seriously disrupting or even damaging satellites in low Earth orbit, such as Starlink, being used in the Russian-Ukrainian war.

Previously known similar systems could operate continuously for no more than three seconds and were much larger. The Russian Sinus-7 drive, for example, was operational for about a second, delivered about 100 pulses per shot, and weighed up to 10 tons.

China has repeatedly signaled that Starlink poses a serious threat to its national security. Chinese military researchers are currently developing new “Starlink killer” weapons, including high-powered microwave systems and lasers, that could be used to relatively cheaply combat large constellations of low-orbit satellites if necessary.

SpaceX has lowered the orbital altitude of its Starlink satellites to reduce the risk of collisions. But that makes them much more vulnerable to attacks from ground-based directed energy weapons. If China eventually deploys the TPG1000Cs in space, the invisible strikes could be even more devastating.

Erika Kirk family DEW Microwave weapon was used to harvest Maduro from Venezuela so the Zionist could cpature the oil and refine it in Citgo refinies in the USA that one of Miriam fiends just bought on the courthouse steps for 7 billion. YOU'RE SLEEPING.Image
Read 11 tweets

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