The meeting was en fuego but something is cooking that may fry the technocracy's plans.
The Mediterranean Sea is experiencing a thermal anomaly so extreme it’s being called a 1-in-216-billion-year event.
To understand how rare that is:
Earth is only 4.5 billion years old.
This heat spike is 48x older than the planet itself.
It’s 15x rarer than the entire age of the universe.
And statistically, it’s as likely as winning the lottery 1,500 times in a row.
So no — this isn’t “just a bad summer.”
This is geophysical madness.
And mainstream science has no explanation.
They’ll blame CO₂.
They’ll say “heat dome,” or “blocking pattern,” or “unusual atmospheric currents.”
But ask them this:
Why is the epicenter of ocean heating located in a tectonically active, magnetically unstable, semi-enclosed basin with active subduction zones and mantle volatility?
They won’t answer — because they can’t.
But CDIGR can.
CDIGR (Core Displacement & Geodynamic Rebalancing) explains this perfectly:
The Mediterranean Sea lies directly above the:
– Hellenic Arc subduction zone
– Calabrian Arc volcanic system
– African-Eurasian compression boundary
– Gibraltar Fault pressure node
All of these are torque points in the planet’s crust — where energy from the inner Earth escapes.
As Earth’s core slowly displaces, angular momentum and internal pressure rise, forcing heat upward through thin crustal zones. This upwelling mantle heat doesn’t just warm the sea — it’s altering ocean density, magnetism, and biological life.
This isn’t from the sky.
This is from deep within the planet.
GRACE satellite data already shows mass redistribution under Europe and North Africa.
Earth Orientation Parameters confirm polar wobble is increasing.
The magnetic field is weakening over these same zones at a tremendous rate.
SST anomalies are appearing exactly where CDIGR said they would: at trench systems, volcanic arcs, and mantle gateways.
This is the Earth screaming through its crust.
Mainstream science offers no mechanism , only centralized pseudoscience explanations tied to the observations.
CDIGR offers a full model, with predictive accuracy and physical logic.
This Mediterranean anomaly is not random. It’s not atmospheric.
It’s the pressure valve of a rebalancing planet.
You can believe in coincidence, or you can believe in pattern.
I warned my Savages that the technocracy has some risks to its power and that Nature would respond.
I told the EU the Mediterranean basis would become a flashpoint.
And now it has.
This isn’t climate change.
This is a core event.
Be ready Savages, Nature's answer to the digital euro, IoT, IoB, and all their nnEMF is incoming.
2. Mainstream media has an agenda to gaslight Earth’s Magnetic Shield collapse and sell you the drama of climate change when it is not. This is how they are managing resources post event for their benefit.
The weaker the magnetosphere, the more solar forcing pushes deeper into the mantle and core via the Global Electric Circuit. As a result, we get an acceleration in Earth’s energy imbalance and it leads to the pictures above.
We’re now getting closer to the water boiling over on the stovetop = more lava and earthquakes where the mantle is rising. But what’s going on between the core and the mantle is more alarming if it reaches a threshold.
What’s the most likely driver of how this is playing out? The poles are moving and weakening the magnetic shield due to a cyclical electromagnetic wave within this region of the galaxy called the Galactic Current Sheet.
This is a more probable case because of the vast electromagnetic changes happening in our solar system and ALL of the planets now, not just Earth. People think the evidence is not in every other planet but it is. The Earth is not doing its own thing like it’s somehow its own closed off vacuum ignoring the solar system altogether. Earth, the sun and the planets are interconnected by this plasma sheet, just as our sun is and this is the stage that this play is being built upon. Many will be part of this coming experience, the next extraterrestrial Event won't be a 6 mile wide asteroid.
3. When the magnetic field weakens on Earth we become a bigger target. If you are jabbed and we get hit with a small solar CME your chances of dying from a heart attack is higher than 3 X. FYI.
4. When the thermohaline currents change the shit is about to get real.
5. When I was a resident I visited several physicists working on the Big projects for the US government in Livingston LA. When I told the DARPA physicist about the effects of transcranial magnetic stimulation on the human cortex, and how it worked in biology, he was stunned.
I did this to illustrate why I believed what I now do about how the human brain functions.
At this point, it would be wise for me to distinguishing regular “magnet therapy” from the effects of transcranial magnetic stimulation. The former magnetic therapy refers to the effects of a static, nonmoving magnetic field from permanent magnets. The latter refers to a magnetic therapy that generates a huge oscillating magnetic field, very close to your head, which induces electric currents in your brain. The movement of the Earth poles induces these currents. I explained to him you can not get a paramagnetic substance any closer to the neocortex then the location of blood vessels and CSF to the surface of the most active cells in the brain or heart. This maximized magnetic effects.
When I was a neurosurgical resident, I visited a physics department where this quantum effect on the human brain was demonstrated to me, for my own amusement. They put a probe near my head and turned the current on and my arms twitched and moved from my shoulder to my fingers against my will.
They were able to activate my neocortex with an oscillating magnetic field!
They turned the magnet field over in polarity, and my arms twitched from fingers to my neck in the opposite direction showing how the DC direct semiconducting current Becker discovered in humans could be reversed when the field was reversed. This is when I realized why pole shifts could destroy living things with magnetic polarity changes.
I then remembered reading accounts where Becker was able to use the same types of magnetic effects to induce complete general anesthesia in animals without ever having an emergency recovery from this type of anesthesia.
6. Does the Earth’s Magnetic Field Generate the DC Current in CSF?
The generation of the DC current is generated in a water layer right below the myelin layer in the CNS and PNS. This interfacial water is directly connected to what occurs at the interface between the neocortex and CSF in light and dark environments. Becker never figured this out, but I have been thinking about what he found for ten long years. I also had the advantage of being a neurosurgeon and operating a lot of brain’s and examining it in all its dimensions with my clinical observations. Any current created within the subdural and subarachnoid space also had to have an associated magnetic field with it, according to nature’s laws. This is why they are called electromagnetic field effects. Electric fields run at 90-degree angles to its associated magnetic field. It turns out this magnetic field has also now been found on the neocortex with the use of MEG and SQUID detectors in the last 20 years.
The electric field was found in the 1930’ s by Hans Berger, who discovered the EEG waves of the brain on our skin. Becker was the first one to hypothesize the presence of a magnetic field in this situation because he was the first one to find that the DC current in humans came from the brain. He also knew all electric fields had to have an associated magnetic field because of Maxwell’s laws. He also knew from his experiments they had to use semiconduction to transmit a small current over long distances below myelin layer and above the axons in the CNS of all vertebrates. He proved biology used semiconduction because his experiments proved the presence of the Hall effect in bone and frozen nerves, which is only found in semiconducting circuits. Because he demonstrated this in the 1960’s, and his work was ignored, he indirectly showed me, why cold was primordial for humans and all life forms that use a DC current to generate energy. This effect has also been found in all plants and trees.
7. DC Current in the CNS/PNS:
Becker showed in experiment that a DC current exists in the interfacial water layer beneath the myelin, linked water chemistry to the neocortex-CSF interface, and they aremodulated by light and dark environments. This demonstrated that a DC electric field exists in biological systems, particularly in the nervous system of vertebrates, and is associated with semiconduction.
Electromagnetic Fields (EMF): According to Maxwell’s laws, any electric current (like the DC current in the brain) must generate an associated magnetic field at a 90-degree angle. This is consistent with the detection of magnetic fields in the neocortex using modern tools like magnetoencephalography (MEG) and superconducting quantum interference devices (SQUIDs).
Semiconduction and the Hall Effect: Becker’s experiments showed that biological tissues (e.g., bone, nerves) exhibit semiconduction, as evidenced by the Hall effect, which is a hallmark of charge movement in semiconductors under a magnetic field. This implies that the DC current in the nervous system operates in a way analogous to solid-state electronics, with implications for energy transmission over long distances. It also explains why CME can cause heart and brain failure acutely in humans.
Earth’s Magnetic Field: While not explicitly mentioned as the source of the DC current in Becker's work, it has been shown over the last 30 years that the Earth’s magnetic field interact with biological electromagnetic systems, potentially influencing the currents or fields in the CNS/PNS/Heart.
Diminishing Magnetic Field: the effects of a weakening Earth’s magnetic field, which is a known phenomenon, as the geomagnetic field has been decreasing in strength over time can easily impact life on Earth.
8. Where we are today in science, in understanding how the brain really works, is close to where a man was 2,000 years ago in trying to understand how the planets moved in relation to the sun.
We are nowhere close to where we should be.
So if we are that far away in our understanding, how can we begin to make sense of it all? We can learn a lot from the macrocosm of space if we scale it to biology on this planet.
My work does that for you, like you have never heard before. I showed you earlier in my blog series how molecular oxygen is delivered from the phytoplankton in the photic zone of the ocean to the ocean depths using the density of cold water to deliver it there.
The more dense the water, the more oxygen is dissolved in it. The power of the sun’s photoelectric effect splits electrons from water in phytoplankton, which liberates oxygen.
The liberated O2 becomes more dissolved in colder water by the laws of nature and chemistry, and then it is distributed all over the oceans by the thermohaline currents.
Today, I am going to show you how the exact same process that happens on the surface of the earth is fractally designed on your own neocortex of your brain.
It is happening right now in the ocean and this effect is huge for those who understand what it means. Normies will never get to this level.
The very same process that works in the thermohaline current works in CSF that surrounds your brain and blood in your heart to bring higher oxygen levels to the surface of your brain using QED principles of the photoelectric effect, water chemistry and magnetism.
9. My analogy above of the science happening on Earth is a progress report or report card and our current understanding of the brain being akin to ancient planetary models is a powerful reflection.
It highlights the vast unknowns in centralized neuroscience, suggesting we’re still at an early stage of understanding how life responds to the cosmos.
My proposal aims to draw parallels between macrocosmic processes (e.g., thermohaline circulation) and microcosmic biology (e.g., cerebrospinal fluid [CSF] dynamics) using fractal design and quantum electrodynamics (QED) principles and I believe it offers a novel framework to understand Nature better than we do.
10. Thermohaline Currents and CSF Oxygen Delivery:
In the oceans, phytoplankton use the sun’s photoelectric effect to split water, releasing oxygen that dissolves more in colder, denser water and is distributed via thermohaline currents. I'm suggesting a fractal analogy where the neocortex’s CSF system mirrors this, with sunlight (or light exposure) influencing oxygen delivery to the brain surface.
The photoelectric effect in phytoplankton involves photons ejecting electrons from water molecules, producing oxygen. In the brain, I am implying a similar light-driven process might occur at the neocortex-CSF interface, possibly via QED (quantum-level electron interactions), enhancing oxygen dissolution in CSF.
11. Density and Oxygen Distribution:
Colder, denser ocean water carries more dissolved oxygen to depth. Similarly, I have proposed that denser CSF, influenced by water chemistry and magnetism, delivers higher oxygen levels to the neocortex. This density effect is modulated by temperature or ionic composition, aligning with physical laws governing solubility.
12. Magnetic Influence:
My earlier discussion of electromagnetic fields (e.g., Becker’s work, MEG detections) suggests magnetism plays a role in biological currents. In this model, the Earth’s magnetic field or the brain’s intrinsic magnetic field might guide oxygen-rich CSF distribution, akin to how geomagnetic forces interact with ocean currents. These have acutely changed now on Earth and nothing alive on Earth realizes it........
13. Inflammation’s Role and CSF Density
I've argued that inflammation reduces CSF density, altering biochemical processes. Inflammation likely increases temperature or introduces solutes (e.g., cytokines, ions), decreasing water density and thus oxygen-carrying capacity.
This disrupts the fractal oxygen delivery system, impairing neocortical function. So a change in thermohaline currents mimics a huge acute magnetic change on your brain.
Less dense CSF fails to support the photoelectric or magnetic effects needed for optimal electron or oxygen dynamics, potentially linking inflammation to neurodegenerative conditions or reduced neural efficiency. This leads to rapid disease generation by raising heteroplasmy. If it happens fast enough and at scale we call this an extinction event.
14. My work in this thread shows you how having an innovative decentralized lens suggests that by studying nature’s large-scale patterns, we can hypothesize about the brain’s hidden mechanisms of how life operates.
15. Given our limited understanding, my approach offers a starting point:
Interdisciplinary Synthesis: Combine insights from oceanography (thermohaline currents), quantum physics (QED, photoelectric effect), and biology (semiconduction, CSF chemistry) to model the brain.
This fractal scaling could reveal universal principles governing energy and oxygen flow across scales.
Experimental Validation: Test the hypothesis with tools like MEG (for magnetic fields), EEG (for electric fields), or CSF analysis (for density and oxygen levels) under varying light and inflammation conditions. Becker’s semiconduction findings should guide experiments on charge movement in CSF.
Macrocosm-Brain Analogies: We need to study how geomagnetic or solar influences affect ocean oxygen and extrapolate to brain responses using light therapy or magnetic stimulation to modulate CSF dynamics.
Focus on Inflammation: Investigate how inflammatory markers alter CSF density and oxygen delivery, linking this to clinical observations from my neurosurgical experience.
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Study Finding: Higher linoleic acid in RBCs correlates inversely (p ≤ 0.05) with five inflammation markers (e.g., cytokines, receptors), suggesting a potential anti-inflammatory effect.
Flawed Conclusion: The article’s claim that linoleic acid is anti-inflammatory assumes causation, ignoring that inflammation depletes linoleic acid.
Mechanism: Linoleic acid, an omega-6 polyunsaturated fatty acid, can be converted into pro-inflammatory eicosanoids (e.g., prostaglandins, leukotrienes) or oxidized into toxic lipid peroxides (e.g., 4-HNE).
Significant inflammation or oxidative stress consumes linoleic acid, reducing its cellular levels.
Nick's Analogy Insight: Like full gasoline cans being absent in burned houses (due to consumption) and present in unburned ones, lower linoleic acid in inflamed RBCs reflects its use/degradation, not a protective effect.
Interpretation: The inverse correlation likely indicates that higher linoleic acid levels are a marker of lower inflammation/oxidation, not a cause.
Decentralized take: Inflamed states deplete linoleic acid, while healthy states retain it to craft UPEs for signaling that become useful to the cell.
Just another way food gurus shit in your cornflakes with bad thinking.
2. Decnetralize Implications?
Implications for RBC UPE
UPE Baseline: RBCs generate UPE (380-450 nm) from ROS via hemoglobin-heme interactions. Healthy RBCs emit lower, coherent UPE (e.g., 700-1100 nm under structured water conditions)
Linoleic Acid Oxidation: High linoleic acid, when oxidized by ROS (e.g., from nnEMF/blue light), increases UPE intensity in the UV-blue range (390-475 nm) due to lipid peroxide formation. This disrupts phase coherence.
Inflammation Effect: In inflamed states, linoleic acid depletion reduces its availability for oxidation, potentially lowering UV-blue UPE but increasing noise from other ROS sources (e.g., mitochondrial dysfunction).
Prediction: Higher linoleic acid in healthy RBCs correlates with lower UPE noise (coherence ~0.8), while inflammation-driven depletion shifts UPE to 390-475 nm (intensity ~0.9, coherence ~0.4). Omega-6 fats thus amplify UPE under oxidative stress but may stabilize it in low-inflammation states.
The biophysics always tells the truth. Food gurus lie.
3. Omega-3 Properties and RBC Context
Composition: Omega-3 fatty acids (e.g., eicosapentaenoic acid [EPA], docosahexaenoic acid [DHA]) are long-chain polyunsaturated fats found in RBC membranes, known for anti-inflammatory and membrane-stabilizing roles.
Contrast with Omega-6: Unlike linoleic acid (omega-6), which can be oxidized into pro-inflammatory eicosanoids, omega-3s are metabolized into resolvins and protectins, reducing inflammation and oxidative stress.
Impact on RBC UPE
UPE Baseline: RBCs emit UPE (380-450 nm) from ROS via hemoglobin-heme interactions, with healthy levels shifting to 700-1100 nm under structured water conditions (coherence ~0.8).
Oxidative Stability: Omega-3s’ double bonds are susceptible to peroxidation, but their incorporation into membranes enhances fluidity and antioxidant defenses (e.g., via glutathione), lowering ROS-induced UPE.
Inflammation Modulation: Higher omega-3 levels reduce pro-inflammatory lipid mediators, decreasing UPE intensity in the UV-blue range (390-475 nm) and preserving coherence.
Prediction: Increased omega-3 levels (e.g., 8-12% of RBC fatty acids, per typical supplementation studies) reduce UPE noise by 20-30% (intensity from 0.9 to 0.6-0.7 at 390-475 nm), shifting the peak toward 700-1100 nm (intensity ~0.7, coherence ~0.85).
This contrasts with linoleic acid, where depletion under inflammation amplifies UV-blue UPE.
So when vegans or Peatatarians tell you DHA is bad for you tell I said to fuck off with their pseudoscience bullshit.
1. Why would anyone listen to MDs who think blocking the sun is wise?
2. The study I am referencing, published in 2016 in Arteriosclerosis, Thrombosis, and Vascular Biology, suggests that UVB exposure may prevent atherosclerosis by regulating immuno-inflammatory responses. This aligns with my point that UV light could influence nitric oxide (NO) production and oxygenation, which are linked to mitochondrial function and NK cell activity.
The idea that a lack of UV light might contribute to conditions like Peripheral Arterial Disease (PAD) and atherosclerosis, and that breathwork and NO support health, is an unknown fact in centralized medicine. Millions of people have died from blocking the sun.
Additionally, UVB's potential to modulate the adaptive immune system has massive implications for autoimmune and chronic inflammatory diseases.
Although the data is nearly a decade old, it highlights a potential gap in current centralized medical paradigms, particularly in specialized fields such as dermatology, lipidology, and cardiology. However, the widespread adoption of such findings requires further research and clinical validation in decentralized medicine, as the laws of physics are clear in their operation.
3. UV light changes the structure of water in your cells to do things you cannot fathom. It builds structures from water to trap energies.
2. I just read what you wrote here Jack. Blew my mind and explains so much. To say it's on the next level of understanding is like saying Nobel Prize work is like college chemistry. I will have to reread to really digest it. Just amazing.
"Food is essentially a conduit for carry information and energy to the gut microbiome to the brain by way of the vagus nerve. Think of your nerves as rivers, and your brain as a lake, into which all those rivers empty. These rivers are filled with water and with light. When “the rivers” arrive at the brain, it decipher’s the quantum light message from the gut, at the leptin receptor. This energy and information then crafts or sculpts the type of gut microbiome diversity based upon the quantum light signal by using quorum frequency sensing. Electrons are how light hitches a ride free of an energy toll in eukaryotes. DHA makes this possible. This is why the photoelectric effect is a key part of healthy eukaryotic life."
What do you really think fen/ben and IVM are doing? They are light sabers. Look at their absorption and emission spectra........I DARE YOU.
3. No one seems to know what makes chemicals carcinogenic and others benign, even when they are chemically similar. In 1970, Fritz-Albert Popp, a German theoretical biophysicist, discovered that benzo(a)pyrene, (a potent carcinogen) , absorbs ultraviolet light at one specific wavelength and emits it at another. Yet, benzo[e]pyrene, a benign polycyclic hydrocarbon known to be one of the most lethal carcinogens to humans, and its twin (save for one small alteration in its atomic molecular makeup). Benzo[e]pyrene is nearly identical twin to benzo[a]pyrene, absorbs and reemits the same light at its original wavelength.
They key to Popp’s research was in the atomic lattice and how light was altered by the atoms. "Small changes in the action of light lead to massive changes in observed reality. Again, we see thermodynamics entering the picture via E=mc2. Popp tested 37 different chemicals in total. The carcinogens “scrambled” light with a wavelength of 380 nanometers. The benign chemicals did not." "Popp later learned that 380 nanometers, the wavelength altered by carcinogens, is also the wavelength that cells prefer to use to photorepair themselves (mTOR).
Fasting and calorie restriction happens naturally via leptin melanocortin signaling and the effect of VDR on the IMM ECT. First principle thinking alone tells you that sunlight does this and lowers GDF15 mimicking calorie restriction. Avoiding Stress-Inducing Activities is also modulated by leptin melanocortin signaling by raising Parasympathetic signaling and controlling SNS. Sleep and recovery are increased by AM solar exposure. The sun is the best way to lower GDF15 and nothing approaches its success.
2. Leptin-melanocortin signaling can modulate autonomic nervous system activity, increasing parasympathetic tone and dampening SNS activity, which reduces stress responses like adrenaline release. GDF15 is upregulated by SNS activation (e.g., adrenaline-induced lipolysis in mice), so enhancing parasympathetic signaling could theoretically prevent GDF15 spikes.
3. Stress reduction via parasympathetic dominance (e.g., through relaxation or leptin-mediated hypothalamic effects) lowers GDF15 by avoiding stress-induced triggers. Reducing SNS activity aligns with reactions of GDF15 lowering to a decreased metabolic stress, decreasing GDF15, The SNS and the leptin-melanocortin pathway act in unison to lower chaos to improve signal fidelity.
The Malate-Aspartate shuttle and its role in connecting cytoplasmic and mitochondrial NAD+/NADH pools are linked to sunrise effects on TCA cycle stoichiometry. This connection arises because circadian cues from sunlight can modulate TCA cycle intermediates (like malate), which the shuttle relies on to maintain NAD+/NADH balance across cellular compartments. NAD+ has a 258 nm absorption spectra and NADH is 340nm. LIGHT is a huge part missing in this story.
2. Ionized Hydrogen (H+) in Mitochondria
Proton Jump Conduction (Grotthuss Mechanism): Within mitochondria, H+ ions (protons) are abundant in the matrix. These protons can move rapidly through water via the Grotthuss mechanism, which involves quantum tunneling. This mechanism allows protons to hop through the hydrogen bonding network, effectively creating superconducting proton cables that facilitate rapid communication.
Ionic Plasma Formation: When hydrogen is ionized, it forms an ionic plasma that behaves like a liquid metal. This plasma, enhanced by iodine, enables efficient charge transport within mitochondria and other cellular fluids like cerebrospinal fluid (CSF). The presence of iodine in CSF, for instance, helps form these superconducting proton cables, linking mitochondrial function to environmental signals.
3. Light Excitation of Electrons:
Mitochondria release infrared light, which interacts with the surrounding water to charge separate it into H+ and OH⁻ ions. This light also excites electrons within the electron transport chain (ETC), influencing the redox state and energy transfer efficiency. The interaction of light with water and mitochondria is crucial for sensing environmental changes.
Magnetic and Electric Fields:
Mitochondria, due to their high density of H+ ions and the presence of transition metals in the ETC, generate strong electric and magnetic fields. These fields can interact with environmental electromagnetic forces, such as those from the ionosphere or solar radiation, to modulate mitochondrial function. The paramagnetic nature of oxygen further enhances this interaction, drawing it towards mitochondria.
DNA's use of helical geometery seems to have a lot on common with the Cosmosi use of electric and mangetic flux in a Birkeland current's organization.
I'm drawing an intriguing parallel between DNA’s supercoiled, torsion-driven structure and the organization of a Birkeland current. Birkeland currents, observed in plasma physics (e.g., in space plasmas or auroras), are helical, twisted flows of charged particles guided by magnetic fields, carrying electric currents along twisted magnetic flux tubes. The sun does the same.
This similarity in helical geometry and energy storage is a fractal I have explored in many blogs. this is why polarization is a big deal. It is why sunglasses are a problem and this showed up in Becker's experiments on sleep.
The Sun and mitochondrial colony is connected in this way wirelessly.
Both systems rely on twist as a stabilizing and functional feature. DNA’s supercoiling stores mechanical torque (10-20 pN·nm) to regulate access and compact genetic material, while Birkeland currents use magnetic torsion to channel plasma and sustain current flow over vast distances.
In DNA, enzymes manage this torsion to control gene expression, akin to how magnetic fields guide and modulate the current in Birkeland structures. The idea of tension gradients in DNA mirrors the dynamic equilibrium of magnetic tension in Birkeland currents, where twist maintains coherence against chaotic dispersion.
Additionally, the role of structured water in DNA stabilization could parallel the plasma environment in Birkeland currents, where charged particles and fields interact to maintain structure.
Both systems suggest a self-organizing principle: DNA’s coil as a biological “engine” and Birkeland currents as a cosmic one, both leveraging geometry and torsion for energy management. While direct evidence linking the two is speculative, the shared physics of helical organization and torque-driven stability offers a fascinating conceptual overlap to explain how life connects to the fabric of the cosmos.
2. Everything in cells have a torsion. It is part of the AMO design inside of a cell which is another key to the mystery of the recipe of Nature. Torsion is the key regulator of energy tunneling: correct twist narrows the energy barrier, boosting tunnelling probability, while loose or damaged coils disrupt conduction. This is quantum control mediated by mechanical tension, measurable in experimental setups.
3. DNA’s selectivity is discriminating by wavelength, polarization, and direction which means it absorbs specific fields. When the right frequency hits, charge conduction increases, water layers shift, and genes unlock, pointing to field-gated biology.
This is why I have a problem with guys like Micheal Levin who say EMF is not a story in biology. This is pur bullshit.
Low-frequency EMFs can unwind or block access, while infrared from mitochondria restores torsional symmetry. Natural rhythms (Schumann, solar, circadian) serve as environmental tuning forks, influencing expression.
Chromatin loops and field-sensitive telomeres organize exposure, and gene expression becomes resonance matching, not just transcription.
Resonant coils store energy, transmit information, and respond to field alignment, mirroring DNA, which stores mechanical stress, converts torsion into access, and tunes to environmental signals. When aligned, this field-aware coil enables life to “speak fluently,” blending quantum biology with measurable physics at the edge of science.