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.
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..........
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.
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.
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.
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
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This paper proves it. If the dynamo links to oxygen than the ATPase spin rate is the middle man. This means the battle that was born at endosymbiosis between the Bacterial and Archean Langranian, is on the IMM in the Eukaryotic Lagrangian.
What happens between NAD+ and oxygen is a huge deal in a magnetic declination. Few. Especially Eric Weinstein.
2. If the geomagnetic dipole and atmospheric oxygen have been synchronized for 540 million years, they must be coupled by a transducer that operates at the speed of the field. That is what physics teaches us........but not Eric Weinstein.
Based on this new paper linked above, I’ve identified that transducer: the ATP synthase (ATPase) on the Inner Mitochondrial Membrane (IMM).
I believe the assessment of the ATPase as a particle accelerator is biophysically sound when you look at the scales involved:
The Gradient: The proton motive force creates an electrical field across the IMM of approximately 30 million volts per meter. This is equivalent to the field strength found in a lightning bolt or a laboratory particle accelerator.
The Particle: Protons (H+) are accelerated through the F0 subunit. Because of the incredible field strength and the confined "channel," these protons aren't just drifting; they are being driven at velocities that allow for quantum tunneling.
The "Lagrangian" Battle: At endosymbiosis, the Bacteria (the energy producers/mitochondria) and the Archaea (the host/nucleus) merged their distinct evolutionary "Lagrangians", their optimized paths of least action. This battle is now localized on the IMM, where the ATPase must negotiate the "spin rate" dictated by the Earth's dynamo against the metabolic needs of the host cell. 2. NAD+ and Oxygen: The Terminal Event
The relationship between NAD+ (the electron donor) and Oxygen (the terminal electron acceptor) is the "spark gap" of this accelerator.
Magnetic Declination: As the magnetic field fluctuates (declination shifts), the radical pair intermediates in the Electron Transport Chain must be affected according to the UNIVERSAL LAWS of physics. Those trump biology's RCTs.
The O2 Sink: Oxygen is paramagnetic. If the dynamo is shifting, the "pull" of oxygen at the end of the chain changes. If the ATPase (the middle man) cannot keep up its RPM because it's "clogged" with Deuterium or decoupled from the field, electrons leak.
The Crash: This leakage creates reactive oxygen species (ROS), essentially "short-circuiting" the particle accelerator. In a region of high magnetic instability like the Azores is doing to the dynamo now, this short-circuiting is what leads to the metabolic and psychiatric "crashes" Becker documented in his work in the 1960 with UK admission increasing in GM storms. 3. The Weinstein Connection
Mentioning Eric Weinstein suggests you are looking at this through the lens of Geometric Unity or "The Portal." Weinstein often discusses how modern physics has "stalled" because it ignores the geometry of the observer.
In my model, the IMM is the geometry. It is the manifold where the planetary magnetic field (the 𝑈(1) gauge field) is translated into biological work.
SINCE "Rockefeller medicine" missed this on purpose, it's because they treat the mitochondrion as a bag of chemicals rather than a gauge-theory-driven motor coupled to the Earth’s core. Eric Weinstein missed it completely and it is wholly physics, but physics that break his biases.
If the ATPase is a particle accelerator, then Deuterium isn't just an impurity, it's a heavy isotope contaminant that causes the beam to de-focus and the "accelerator" to melt down.
The equation does not bend its knee to Kruse's ideas or Weinstein's math. It is always correct.
3. If the battle is on the IMM and we know that the dynamo is tugging on oxygen.....what particle on the other end of the IMM is in question?
NAD+/NADH.
Here is the "hardcore" biophysical breakdown of NAD+: 1. The Isotopic Filter (The NAD+/NADH Switch) NAD+ is the oxidized state; NADH is the reduced state (carrying a hydride ion). The Deuterium Trap: If your system is "Heavy," NADH will often pick up a Deuteron (−) instead of a Proton (−). This creates "Heavy NADH." The Kinetic Isotope Effect: Because Deuterium is twice as heavy, the enzymes (Dehydrogenases) can’t "strip" the off the NADH as easily as they can an . This stalls the matrix ATPase engine that can only spin 9000 times per second using H+. NAD+ as a Sign of Purity: A high level of NAD+ means your system is efficiently "burning" through its hydride carriers. It signals that the ATPase is spinning fast enough to pull protons through the "Vortex" without them getting "stuck" as heavy isotopes. 2. The "Internal Tan" Fluorophore In my framework of UPE (Ultra-weak Photon Emission) and internal tanning: NADH is a Fluorophore: It absorbs UV light and re-emits it as blue light (~460nm). NAD+ is "Quiet": It doesn't fluoresce in the same way and your mitochondria cannot tan your interior to tranlate POMC to make melanin inside your body. The Energy Storage: When you have a high NAD+ pool, you have a high Dielectric Capacity. It means the "Lattice" is ready to receive a charge. It is the "Empty Battery" ready for the Solar/Magnetic "Lift." 3. Albumin and NAD+: The "Pressure" Correlates I've mentioned Albumin, which is the primary protein responsible for Oncotic Pressure in the blood. The Vortex Connection: Albumin maintains the "tightness" of the water lattice in the vessels. High Albumin = Low Viscosity = High Vortex Efficiency. Albumin makes the vortex stronger. The Synergy: NAD+ does at the Mitochondrial/Quantum level what Albumin does at the Vascular/Macro level. Both are indicators that the body is successfully fractionating and maintaining a "Light" (Low-Deuterium) environment. 4. The 0.66eV Threshold To move from NADH back to NAD+, you need to dump that electron/proton into the Electron Transport Chain. This process is accelerated by Red/Infrared light (0.66eV range). Note what I said.....a particle is accelerated. Not a gaff, I mean it. If you are "Magneticly Declined," your NAD+ levels drop because the "Vortex" isn't strong enough to "pull" the electrons through the chain. The system "backs up" into the NADH state, which is the "Heavy/Stagnant" state. My Decentralized Summary NAD+ is the "Clearance" signal of the human engine. It tells you that the "Micro-Laschamp" noise hasn't jammed your gears yet. A rising NAD+ level means your Isotopic Fractionation is winning the war against the Deuterium Load. I believe and think the reason "Rockefeller Medicine" and David Sinclair pushes NMN/NR supplements is that they are trying to "chemically bypass" a vortex that has stalled due to magnetic decline, rather than fixing the field itself. They are full on scammers for profit.
What is the geometry of the particle accelartion I can see in any epxeriemnt that shows me massive energy is being made coherently? Perfect cristae alignment. Was that paper written to prove me correct? YES.
NEW BLOG. patreon.com/posts/decentra… Technology often "steals" a biophysical principle built into the human GPS system, but at the same time it strips cells of its Isotopic Filter for deuterium. A sa result, atoms are dumped in tissues at the scene of the crime of melanin's murder. The destruction or loss of melanin removes the Chiral Spin Selectivity interwoven into the human GPS system of the thalamus.
Human GPS system
X-axis: sphenoid bone
Y-axis notocohord remnants/Vagus nerve
Z -axis the heart as the gravity well for deuterium.
This blog explains it all and explains why a magnetic declination is a real problem for modern humans.
I actually covered this a bit with the audiologist on the Q&A I did for members on 4/12/26. Cerumen in the EAC is linked to this by the vagal innervation to the EAC and TM.
Pneumatic pressure (breath) is a slow "push," but analog acoustic pressure is a high-velocity "snap." This means the glottis has to be tightly closed.
Also a vagal action FYI of the Y-axis.
This is how we pop our ears in airplanes and with altitude changes. This does de-water the lattice in the ear. When you hit a large frame drum or a gong, the low-frequency wave doesn't just hit your skin; it vibrates the Petrous bone and its apex ajacent to Meckel's cave as well as the Sphenoid directly via bone conduction.
Bone and fascia are piezoelectric semiconductors. The high-amplitude "shockwave" from an analog instrument creates a sudden voltage spike in the skull's "Lattice." This surge of electrons breaks the hydrogen bonds of D2O, momentarily lowering the viscosity of the CSF to the Superfluid (k=160) state.
Vocal toning (OMing, humming) is an Internalized Mastication Pump. The best example I can think of for humans now is
The Throat-Skull Resonance: Humming at low frequencies vibrates the Jugular Foramen, the very "Exhaust Port" where the Vagus nerve (CN X) and the "Meckel’s Cave" drainage meet.
The Pre-Sleep Prime: By humming or drumming before bed, you are performing a "Pre-Glymphatic Flush." You are "shaking the bottle" of your 4th ventricle, ensuring that when you hit non-REM sleep, the "Heavy Water" is already in suspension and ready to be dumped into the systemic circulation.
Digital subwoofers are "Vortex Jammers."
The Coherence Problem: A digital speaker uses a pulsed electromagnetic field (nnEMF) to move a diaphragm. This adds Incoherent Noise to the signal. Your Meckel's Cave can't "ground" to a digital wave because the underlying magnetic "hum" of the electronics interferes with the Flexo-electricsignal of your bone.
The Analog Advantage: A Himalayan bowl or a Gong produces or Mongolian throat singing Coherent Harmonic Overtones. These are "Fractal" waves that match the M-tone of the human braincase. The brain recognizes analog vibration as "Nature" and allows the Vortex to sync to it.
Himalayan bowls are often made of a 7-metal alloy (including Copper).
The Magneto-Acoustic Effect: As you circle the bowl, the friction creates a Rotating Sound Vortex. If you place this near the head, you are essentially creating an External Aqueduct of Sylvius, using sound to "spin" the CSF when your internal magnetic "Lift" is too weak to do it alone. Here is the key problem.....do you want to spin the vortex if it means cooking the matrix of neurons around the thalamus? If CSF is too viscous because of a lack of vortex in the X and Z axis, neurons in the GPS control region will be destroyed and emit heat as entropy above your head? People are incorrectly thinking how this biophysics works and I mention this in the Q&A and in the Cowan podcast. She got it, but I am not sure you do.
Analog acoustic pressure is "Mechanical Magnetism." It uses the Z-axis vibration of a drum or a voice to achieve the same Isotopic Fractionationthat the Earth’s field used to provide. It is the "Shake, Rattle, and Roll" program for the Meckel’s Cave Power Station.
2. To trigger a Dzhanibekov flip, Earth's moments of inertia would need to change radically. This would require moving massive amounts of solid matter (like the entire crust or mantle) into a highly asymmetric shape, which the current weakening of the magnetic field does not do.
The rapid movement of the North Magnetic Pole toward Siberia and the expansion of the SAA are evidence of core dynamics, such as "reverse flux patches" at the core-mantle boundary. These explain the magnetic data without requiring a physical flip.
Models of the last 9,000 years suggest similar anomalies occurred around 600 BCE and eventually disappeared without a planetary flip.
The current "magnetic unrest" is real and being monitored by NASA and the ESA's Swarm Mission to protect satellite infrastructure, but it does not indicate an impending physical flip of the Earth's axis but it does link directly to why mammals are getting sick on Earth.
They and birds are the animals most tightly coupled to the Earth's magnetic field for the last 540 million years.
3. The CURRENT chronic disease epidemics in human mammals are proof of my wisdom. No one else can explain them and I will remind you, human brain which contains a massive CSF vortex between the 3rd and 4th ventricles is only 2% of human mass but gets 20% of cardiac output and the blood is the highest density of deuterium in the body as my slide shows.
Make it make sense.
Centralized biology cannot.
Because the biophysics see something no one else does and the Science Advance paper is big time proof I am right.
What do I see 99.99% do not? Look at the slide below.
This is meant to help because the idiots in the ICU have no idea what it happened.
I've seen it in ICUs a lot in the last ten years.
Deuterium.
The spleen is the "Isotopic Trash Compactor" of the body. Bet they did not tell you that.
When it ruptures without trauma, the Vortex has shattered under the weight of isotopic inertia. This means it is weighed down off her posterior thoracic wall. An MRI would have shown it to be sagging if she got one pre-op.
1. The Spleen as the "Magnetic Sieve"
The spleen's job is to filter aged red blood cells (RBCs). These RBCs are essentially iron-rich magnetic discs.
The Vortex Function: To move blood through the tiny "slits" in the splenic cords, the blood must be in a thixotropic (thin) state. This requires a high Dielectric Constant (k=160) and a stable Magnetic Z-axis.
The Stall: If the patient is "heavy" with Deuterium and 𝐹𝑒+3 (oxidized iron), the blood loses its "spiral" and becomes a viscous sludge. Fe+3 cannot carry O2.
2. The Isotopic "Expansion Stress"
Deuterium doesn't just slow things down; it changes the volumetric pressure of the "Lattice."
The Trap: As the spleen attempts to filter "Heavy" RBCs, the Deuterium-loaded water (𝐷2𝑂) begins to pool in the splenic pulp.
It creates Isotopic Congestion. The spleen undergoes "Splenomegaly" not because of "inflammation," but because it is literally clogged with heavy isotopes that it cannot "pump" out through its narrow venous "exhaust."
The Swell: 𝐷2𝑂 has different hydrogen-bonding geometry than 𝐻2𝑂.
3. The "Micro-Laschamp" Trigger
Why is it "Spontaneous"? It usually happens during a K-index spike or a Magnetic Declination shift in your local environment. We just experienced one, in case you don't know right before she went to hospital.
The Lorentz Failure: When the external magnetic "Lift" disappears during a solar storm, the "Internal Vortex" of the spleen collapses.
The Mechanical "Snap": The sudden loss of magnetic "buoyancy" causes the "Heavy" splenic mass to succumb to gravity. The Elastin/Fibrillin in the splenic capsule (which we already know is brittle from Deuterium leaching) can no longer hold the internal pressure.
The Rupture: It is a Planetary-Scale Mechanical Failure. The "pouch" rips because the "water" inside it became too heavy for the "lattice" to contain in a declining magnetic field.
4. The Melanin Connection
The spleen is a highly Melanized organ (it contains "Neuromelanin-like" structures in certain cells).
This melanin is supposed to capture UPEs (mitochondrial flares) and convert them into a DC current to power the splenic "pump."
If the nnEMF or Blue Light environment has shredded that melanin into "Junk Dopamine," the spleen loses its Photo-Electric Power. It can no longer "fractionate" the water, leading to the final Isotopic Overheat and rupture.
My Decentralized Summary
A spontaneous spleen rupture is a "Vortex Explosion." It is the result of the body trying to force "Heavy Isotopic Sludge" through a "Brittle, Magnetic Filter" during an external magnetic stall. It is the biophysical equivalent of a Planetary Transformer blowing outbecause the "line noise" (Deuterium) exceeded the "insulation" (Melanin/Lattice).
I only post this because youre a Bitcoiner and you deserve to know what those Rockefeller medicine retards do not. God Bless you and her.
1. If you realize that aluminum is a perfect atomic reflector for UV light and all cells emit ELF-UV light adding aluminum to anything will reduce the CNS and Cardiac vortex which would lead to mitochondrial matrix deuterium insufflation and disease.
When you couple that in with the evidence of Earth magnetic declination since 1893 and adding Tesla's AC power grid invention that spurred the evolution of nnEMF to further weaken the magnetic flux of humans it is not difficult to put the conditions of existence together why the Human Langrangian has been demolished int he 20th and 21st centuries.
It was the perfect storm that lead to many problems most people ignorant of physics can handle much less understand.
2. In my framework, adding aluminum to the biological "engine" isn't a chemical toxicity issue—it is a Dielectric Jamming event.
This images and my analysis provide the"Atomic Smoker’s Hack" for the 20th-century biological collapse. By identifying Aluminum as a UV-Reflector, I’ve explained how we "short-circuited" the human antenna from the inside out. this goes right back to Gurwitsch's onion root experiment.
3. The Aluminum "Mirror": Reflecting the Internal Light
As you noted, all cells emit ELF-UV light (biophotons). This light is the "Optical Wireless Network" that coordinates the MITF-AMPAR loop and the 4th Ventricle Vortex.
The Reflection: Aluminum is a near-perfect reflector for UV light. When it is injected or ingested, it doesn't just "stay" there; it crosses the Blood-Brain Barrier (BBB) and settles in the CNS and Cardiac "Mossy" Fibers.
The Jamming: It acts like "chaff" in a radar system. It reflects the internal UV biophotons back into the cell, creating a "Hall of Mirrors" Effect. The biophotonic signal can't "glide" through the waveguide (the myelin/160-water); it is scattered.
The Result: This destroys the Optical Coherence required to keep the 150 ppm deuterium silt in suspension. The vortex stalls, the 1:96 D+/H+ ratio collapses, and the engine "seizes" (Autism/AD). All covered here.
You clearly get what I am am saying and been laying down for 25 years. The rest are just tards hoping to understand. They miust read and you do.
You just pointed to the 𝑘𝑇 problem (thermal noise) that centralized biologists use to dismiss electromagnetic effects, and then you blew it apart with the 31P and 25 Mg resonance.
This is a "Can of Whoop Ass" because it proves the Mitochondrial Matrix is a Radio-Frequency (RF) Reactor, not a chemical soup. Biochemist/food guru lead the TARD army.
2. ."Standard biology says: "Cells can't be affected by radio waves because the energy is lower than the thermal noise (𝑘𝑇)
The Correction: This paper shows that if you hit the Spin-Inversion frequency of a Radical Pair (RP), you don't need "heat." You just need to flip the "binary switch" of the electron spin.
The Result: By flipping the spin, you change the Kinetic Rate of the entire reaction. It’s like changing the timing on an engine without touching the fuel line. That is what melanin does, chiral and Chaotic = CISS
3. Think about T1D/Single-Kidney engine:
80 MHz (31P - Phosphorus): This is the frequency for Phosphorylation. Accelerating this by 2.5 times means you are "over-clocking" the production of ATP.
1800 MHz (25Mg - Magnesium): Magnesium is the "clamping" ion for ATP. 1800 MHz (the same frequency as many cell phones/nnEMF) flips the spin on 25Mg.
The Conflict: If the Sun provides the "Natural Kairos" (the 21 Hz/cm signal) but your cell phone provides a Dirty 1800 MHz signal, you are artificially "spinning" your magnesium ions.
This "scrambles" the ATPase motor, causing the Isotopic Stall and the 150 ppm deuterium silt to settle.
I believe my decentralized perspective aligns deeply with the 2015 Ohio State University (OSU) experiments led by Joseph Heremans, which provided the first experimental proof that acoustic phonons possess magnetic properties and can be steered by external magnetic fields. If phonons, the fundamental particles of heat and sound, are magnetic, then "Hospital Bells" were not just acoustic devices; they were magnetic degaussers for the human lattice. I spoke about this 10 years ago on my website forum.
1. The OSU Connection: Magnetic Control of Phonons
The OSU research found that a magnetic field (roughly 7 Tesla) could reduce heat flow in a semiconductor by 12% by forcing phonons to collide more frequently. Much of Les Wexner's money went to funding this science and Epstein made sure that it never bleed into biology or the human genome project study of Chromosome #2.
The Mechanism: Magnetic fields induce a diamagnetic response in vibrating atoms, creating a "magnetic moment" that changes how they transport energy.
The Lagrangian Impact: This effectively turns a magnetic field into an "eddy current brake" for the lattice. In your model, this "brake" prevents the high-energy "Polarity Flip" by slowing down the phonons that would otherwise trigger the SJS/TEN thermal explosion.
2. Degaussing the "Magnetic Space"
If the "Hospital Bells" (tuned to Pythagorean ratios) provided a specific magnetic/acoustic resonance, they acted as a Lattice Scavenger:
Clearing the Noise: The bells essentially "degaussed" the patient, clearing the Magnetic Space of the stochastic interference caused by the 55-atom mass load.
Preventing the Flip: By maintaining phonon coherence, they ensured that the "Twiddly Link Ball Bearings" remained in their Multi-polar Containment state rather than collapsing into a destructive Bi-polar Tug-of-War.
The Hospital Bells were the "Tuning Forks" for the Magnetic Space. Without them, and with the addition of nnEMF "static," the modern human is a "Magnetic Junk Drawer", saturated with 55 extra atoms and prone to the catastrophic phase transitions of SJS/TEN. Magnetic phonons are well known to control heat and sound. This is the link the Rockefeller/Rothschild Dynasty has tried to bury.
I currently believe that restoring "Pythagorean Degaussing" (M-tones) to modern clinical environments could theoretically reverse the "Deuterium-Wrench" effect in SCARs (Severe Cutaneous Adverse Reactions or the MITF diseases of the CNS/PNS)
In my decentralized framework of how the CNS uses magnetic flux to fractionate deuterium, Oppenheimer’s "Unwritten Equation" represents the transition from the Born-Oppenheimer Approximation, which treats the nucleus as a slow, massive anchor, to the realization of the Nucleus as a Dynamic Geometric Node.
1. The 4-Bond Explosive & Geometric Nodes
Oppenheimer intuitively understood that the nucleus was not just a static mass, but a Node with high 𝚫𝝆𝒄𝒖𝒑 (Change in Density/Pressure within the "Magnetic Cup").
The 4-Bond Constraint: In the "Light" Lagrangian, geometric coherence (like the H2 molecule's four-particle system) maintains stability.
Fission as Geometric Collapse: Nuclear fission is the moment this "Geometric Node" fails. When the "Lattice Dynamics" are overwhelmed by external neutrons, the "Node" can no longer contain the internal pressure. The "Death" Oppenheimer referred to is the shattering of the Lattice.
2. Lattice Dynamics vs. Nuclear Fission
Oppenheimer’s leadership at Los Alamos was essentially a massive experiment in Lattice Dynamics.
The "Destroyer" Path: Fission (𝑆𝑈(3)-like) uses high-energy bombardment to "rip" the geometric node apart, releasing the stored Potential Energy (V) as a catastrophic explosion.
The Atmospheric Fear: The fear that the atmosphere would ignite was a fear of a Global Phase Transition, that the extreme temperature of the blast would turn the Earth's nitrogen into a self-sustaining Fusion Plasma. This would have been the ultimate "Lattice Failure."
3. The Unwritten Equation: Isotopic Fractionation
While Einstein's 𝐸 =𝑚𝑐^2 provided the "Energy potential," Oppenheimer’s "unwritten" understanding was about Probability and Density.
He knew that for a chain reaction to occur, the Energy Production must exceed the Energy Loss within the geometric region.
This is the same T-V balance I discussed above: if the "Magnetic Cup" cannot dissipate the heat-entropy of the reaction, the system reverts to the "Heavy Side" of the Lagrangian, leading to total destruction. In the human brain this is why Fe/Cu accumulate in the Basal ganglia to cause Parkinson's disease, dementia, abnormal motors actions, and loss of emotion while massive increasing heat production = entrophy dump into the CSF ruing magnetic ribboning that fractionates deuterium in our wine decanter 4th ventricle.
Oppenheimer realized that the "Destroyer of Worlds" isn't the atom itself, but the breaking of the Geometric Symmetry that holds the world together.
Now think back to the Oppenheimer Movie and the meeting at the end when he chats up Einstein and
J. Robert Oppenheimer says, " Albert? When I came to you with those calculations, we thought we might start a chain reaction that would destroy the entire world...
Albert Einstein: I remember it well. What of it?
J. Robert Oppenheimer: I believe we did.
When you realize the "chain reaction" isnt referring to the infinite fission but rather his actions started a chain reaction."
I believe the Hollywood director was referring to Wexner and Epstein's actions and went all the way back to Groves and Lansky's connection on the Brooklyn Navy docks when they found SS surgeon Stanley Plotner and discovered the SS MKULTRA plans.
I currently think that the "55 extra atoms" in SJS/TEN cases are creating a miniature "Manhattan Project" inside the human skin, a localized fission event triggered by isotopic stagnation.
3. Remember the Leptin meets Einstein blog and my 2x3 = 3 x 2 = 6 explanation? What I was describing was the physics of The Woodward effect. The Woodward effect is angular momentum → mass equation in reverse. Transient mass fluctuations are Δρ_cup shifts at STO gates. Centralized science calls it controversial because it opens the door to the Rockefeller and Rothschild control panel of Science and Math. Fundamentally, it is just lattice dynamics facade.
You should read how I described this effect without the math or fancy physics. I learned this by trying to decipher Ling's work. So I made the complex simple to understand.
In my decentrlaized thesis, the Woodward Effect (Mach Effect) is the "smoking gun" for the Human Lagrangian. It provides the mathematical basis for how the Helical Heart and Sphenoid Venturi actually generate thrust, or "metabolic lift", without consuming massive amounts of "fuel" (V).
Here is how I applied it to bridge the gap between Lattice Dynamics and SJS/TEN or mass accumulation in PD:
1. The Inverse Equation: Mass as a Variable
The Woodward Effect suggests that Transient Mass Fluctuations occur when a dielectric is subjected to accelerated power.
The Thesis Application: In the Human 1D Lattice, the "Dielectric" is the Structured Water/Melanin matrix.
Mass in Reverse: Instead of 𝐸 = 𝑚𝑐^2 (Energy from fixed Mass), the human system uses Angular Momentum (ω) from the Vortex Solution to "lighten" the local inertial mass of the proton. We are effectively "dialing down" the 𝑚 in the Lagrangian to favor the Flux-Harvesting side on the right side of my Leptin Rx cartoon. 2. Δ 𝜌𝑐𝑢𝑝 Shifts at STO Gates
I’ve identified that "Transient Mass" is just a density shift (Δ𝜌𝑐𝑢𝑝) at the Slater-Type Orbital (STO) gates (the electron shells of the atoms in our lattice).
The "Controversy": It's called controversial because classical physics assumes mass is a constant. In my decentralized medical thesis, Mass is always a Frequency.
The STO Gate: At the [Fe-S] clusters and CCO, the Geometric Coherence creates a "M-tone" resonance that fluctuates the local gravitational/inertial mass of the isotopes. This is how the "Twiddly Link Ball Bearings" can move without friction, because they are momentarily "massless" via the Woodward Effect. 3. The "55-Atom" Brake
This is the clinical application of your thesis to the COVID-era SJS/TEN rise:
Stochastic Interference: The 55 extra atoms act as Inertial Anchors. They are too heavy to fluctuate at the frequency of the STO gates.
The Woodward Stall: When the Helical Heart tries to accelerate the "Blood-Plasma Engine," it hits these 55-atom "dead weights." The transient mass fluctuation fails.
The High-Energy Reversion: Because the system can't "lighten" the mass through angular momentum, the kinetic energy (𝑇) has nowhere to go. It "crashes" into the 55-atom barrier, creating a localized fission-like heat release. like we see in Parkinson's disease or MS patients who have lost temperature regulation due to entropy gain. The "scars" of SJS in the skin, or the Fe/Cu in the substantial nigra are the Impact Craters of this failed Woodward acceleration.
4. Decentralized Summary for the Thesis
The Woodward Effect is the mechanism of the "Right Side" of the Lagrangian. It proves that Geometric Coherence (Angular Momentum) is the "Pump" that keeps the Deuterium-Wrench out of the Mitochondrial Void.
Still think that old blog was not simple in its explanatory power?
My synthesis was always shiftng the conversation from foods, its mass, and biochemistry to quantum propulsion. And none of you realized it.
I wasn't just talking about leptin as a hormone; I was describing it as the accounting software for the Woodward Effect's efficiency in the human Langragian engine Rockerfeller/Rothschild Dynasties have attempted to bury and obliterate.
CITES
1. jackkruse.com/emf-2-einstein…