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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What do you know about the Stiles-Crawford effect in a healthy eye? What if I told you this effect is how we sharpen central vision and narrow the periphery of the retina from too much blue light. Would you believe it? Did you know melanopsin has a specific topographic map on a healthy retina? A lesson no has taught you is incoming.
2. All opsins are topologic insulators. You might want to read that threadroll above now to understand topology well.
Topology changes in a cell = geometry change of cristae = UPE change from mitochondria = the optical signal changes in the same tissue altering physiology.
So what happens if you sustain mitochondrial damage in your retina's colony of mitochondria to the Stiles Crawford effect?
What are the implications?
3. The Stiles–Crawford effect (SCE) is the human eye's phenomenon of reduced light sensitivity when light enters the pupil from its periphery compared to the pupil's center. This effect is due to the optical properties of photoreceptors, which act as waveguides and are aligned to channel light towards the fovea, the central point of vision. The SCE makes vision less sensitive to light entering the periphery, thus reducing glare and improving visual clarity. It also keeps a lid on the amount of blue light the periphery the retina gets.
This sharpens vision, makes myopia, glaucoma, cataracts, hyperopia, and AMD almost impossible to get. Makes one resistant to mental illness too. Makes one impervious to diabetic transformations. Makes neurodegeneration rare.
Another new podcast from me with Smuggling Hope. It is good one on mental health because it explains how biomolecules absorption and emission spectra's determine reality or determine which mental illness one gets.
This is the information why Jordan Peterson is sick and why he and his daughter have stumbled multiple times in getting him well. ivoox.com/.../exposing-t…...
Biophotons are ultra-weak light emissions produced by living organisms, thought to arise from metabolic processes like oxidative reactions in mitochondria. Centralized scientists and AI bots hypothesized them to play a role in cellular communication, potentially influencing gene expression or signaling pathways. FIAF, also known as angiopoietin-like protein 4 (ANGPTL4), is a protein produced by tissues like fat and the gut, and it’s a key player in lipid metabolism and microbiome construction. Neither understand how UPEs control FIAF. If the UPE is coherent then FIAF inhibits lipoprotein lipase, affecting how fats are stored or broken down, and its expression ramps up during fasting. The microbiome, meanwhile, is the community of gut microbes that can shift in response to diet, fasting, or host metabolism, influencing energy balance and health. If the UPEs in mitochondria is not coherent, the UPE changes and mental illness becomes more probable. You cannot burn fat so it changes neural signaling.
Centralized scientists and technocrats who build AI systems will say no direct study says “biophotons control FIAF to affect the microbiome,” but we can hypothesize based on related mechanisms. This is patently false. Why?
FIAF has known absorption and emission spectra to light frequencies. Because of that, a study is superfluous because each chemical in the world has an optical fingerprint. Just because a scientist has not published the work is immaterial to this BASIC biophysical fact in spectroscopy. This was what I brought Ray Peat over ten years ago, and he was impotent enough to answer my critiques of his work. This podcast covers these details.
2. Is nerve pain caused by a Lyrica deficiency?
Is Lyme disease linked to a lack of doxycycline?
Is depression due to Prozac deficiency.
Are heart attacks are due to Lipitor deficiency.
Is obesity due to Ozempic deficiency.
Are Headaches due to Tylenol deficiency?
Is Bipolar disorder due to lithium deficiency?
Any questions?
You've been conditioned by centralized medicine to ask the wrong question.
You have a solar deficiency combined with a nnEMF toxicity problem.
This alters the UPEs your mitochondria make and it is this light that changes the neural tracks that make you mentally ill. This is why your Bipolar Disorder exists. The defect is not in you; it is in your environment.
3. Light exposure,say, sunlight or specific wavelengths impacts circadian rhythms via the suprachiasmatic nucleus in the brain, which regulates hormones like dopamine, GABA,melatonin and cortisol.
These hormones influence metabolism, including fat tissue activity where FIAF is expressed. Metabolism is what makes the key UPEs.
Fasting, which boosts FIAF, is also tied to light cycles, think of how daylight affects feeding patterns. If biophotons reflect or amplify these light-driven processes at a cellular level, they might indirectly tweak FIAF production by signaling energy states or oxidative stress in cells. If you cannot burn fat you are more likely to be mentally ill.
My decentralized ideas have always been spot-on that this topic doesn’t need a scientist to spell it out in a paper, absorption/emission spectra are measurable, and biophoton emissions are detectable.
The gap isn’t in the physics; it’s in tying the specific wavelengths of biophotons (which vary by cell type and state) to FIAF’s exact optical profile in vivo. Still, if gut cells emit biophotons in, say, the 300-400 nm range, and FIAF absorbs there, the optical photonics interaction’s real, study or not. It is first principle thinking. It is obvious what they problem. It’s like saying water absorbs infrared; we don’t need a new experiment to prove it gets hot under sunlight. Biology acts like it does, but in physics they use theoretical physics and first principle thinking to make predictions when the experiments are not done or cannot be done.
When matter experiences this topologic change do you know it become capable of emitting photons? In biology we call this UPEs. That is what does all the information transferring in life to keep you alive and kicking.
2. In astronomy and cosmology Spectroscopy is a form of remote sensing, meaning it allows scientists to determine the composition of an object without physically interacting with it. This is how we examine remote atoms in deep space.
How do we know what other worlds are made of? Planets we’ve never touched, stars we’ll never reach? By reading their light. Why can't quantum biologists realize the same opportunity exists in cells?
3. Quantum biology cannot yet apply the same spectroscopic "reading of light" as astronomy because cellular components are too small to be analyzed by light in the same way, and the inherent quantum effects within cells are not easily distinguishable from background noise in typical biological systems. They do not have photomultipliers small enough to sample UPEs yet.
Just because the technology is not available or studied means we should ignore the idea. Absense of evidence is not absence of effect. This is first principle thinking that is missing from most scientists today. In physics theoretical physicists provide a first principle lens to the Standard Model to innovate. We need to do the same in quantum biology. This is what I do.
Astronomers use spectroscopy to analyze the wavelengths of light absorbed or emitted by large celestial bodies, which reveal their chemical composition. However, cellular molecules are often too small to generate a detectable light signature, and the complex, noisy environment of a living cell makes it difficult to isolate and interpret the faint quantum signals associated with specific biological processes. there is no doubt today UPEs are real and carry information. We've know that AXIOMATICALLY since the Onion root experiment in 1922.
Cutaneous antimicrobial effects of sunlight on cholesterol conversion to Vitamin D components are today's PSA boys and girls.
1,25(OH)2D made in the liver and kidneys from 25 D(OH) from the skin by the sun and cholesterol and its receptor regulate the processing of the long-chain glycosylceramides that are critical for the skin barrier formation which is crucial in defending the skin.
Do you know how the heme protein enzymes CYP control this process?
The two Vitamin D biomolecules induce toll-like receptor 2 (TLR2) and its coreceptor CD14, which initiate the innate immune response in the skin. Activation of these receptors leads to the induction of CYP27B1 (heme protein), which in turn induces cathelicidin resulting in the killing of invasive organisms.
What happens when blue light and nnEMF destroy heme proteins when you know this connection? Innate immunity is destroyed. This is why Fauci wanted you indoors during COVID he and Baric made in Ukraine and China. ncbi.nlm.nih.gov/pmc/articles/P…
2. See how the heme photoreceptors are blown away?
3. Spine tumors are not common but most of them are associated with a poorly functioning immune arm and associated with low Vitamin D levels from poor solar exposure. That is something you can prevent to avoid this outcome.
Fire your centralized doctor by hiring nature for your reversal! Nature quantizes the precise amount of melatonin from the mitochondria needed to optimize autophagy and apoptosis. 95% of melatonin is made in human mitochondria. It is not your pineal or your gut. Your central retinal pathways have more mitochondrial density in it than any other part of the brain. The same is true with DHA to run your SCN faster than the other molecular clocks in your body to meet relativity needs. Want more info on exogenous melatonin? Use Yandex search with my name and mitohack #722. Your welcome in advance.
2. Shall we also say that sunlight plus natural darkness at night control melatonin, which in turn controls HIF-1a, which in turn controls sensing of O2?
Guess what happens to your mitochondria when oxygen tensions change? The IMJ geometry changes, metabolism morphs, geometry alters, and UPE become less common but more coherent. Mitochondria can change their physiology when the environment changes too. This is a remnant of the GOE when we had chronic hypoxia. this is why we innovated HIF1 and linked it to the PER clock genes.
Did you know UV light exposure raises oxygen tension in the venous plasma?
Guess what that all implies?
I know a lot more than any centralized MD or PhD about how we really operate.
If you have a T1D child you have a light problem. That light problem has manifested in your germ line.
If you're a Type 1 diabetic, by defintiion you have a chronic UVA and UVB deficiency and a chronic overdose of artificial blue light and nnEMF. It is also axiomatic.
Look at the chart below. T1D is almost nonexistent near the equator
2. By around 20 weeks of pregnancy, a baby girl’s ovaries already contain every egg she will ever carry.
Which means that when your grandmother was pregnant with your mother, the cell that would one day help form you was already there.
Three generations, held in one body.
This isn’t folklore. It’s embryology.
Pregnancy is sometimes called a three-generation event: grandmother, mother, child, all sharing the same environment in a single moment. Scientists call it multigenerational exposure. I call transgeneration biology.
3. But biology makes it hard to imagine these things don’t matter. The oocytes that hold potential life are shaped by the whole soup of environment, and so are the children they become:
☀️ Light and circadian rhythm
🌊 Water quality
🥬 Nutrition and minerals
🌬 The air we breathe
💊 Medications and substances
💤 The quality of rest and sleep
💭 The emotions we carry
🧲 Electromagnetic fields and magnetism
🧪 Toxins and chemicals
Even mitochondria, not just “batteries” but regulators of repair, signalling, and survival, are passed down the maternal line. It is an unbroken inheritance that centralized medicine continues to ignore at your peril.
Three generations are intertwined in every pregnancy in humans.
Biology is carrying echoes of what came before, and the possibility of restoration.
Parents need to become conscious of these risks to eradicate these diseases. The transhumanists seem to know, why don't the normies?