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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1. Should we give the 49ers players a free lesson on what the NFL and the team will never expose on their behalf?
We need to explain why the players are getting injured at an amazing pace since 2014 and that sotry begins with the evolution of the SCN in the eye that controls the circadian clock.
The eye clock is the key to the story of their injuries.
2. Today we know that vision and hearing evolved together dating back to the PaxB gene, which is a single gene controlling eye and precursors to hearing (mechanoreceptors) in box jellyfish.
This occurred before independent Pax 2 and Pax 6 genes showed up in primates much later. There are evolutionary connections between eyes and mechanoreceptors of the inner ear to the extent that during evolution are linked to melanin generation in those sense organs.
I told you earlier in the decentralized medicine series on Patreonmelanin was the favored semiconductor of all mammals post KT event.
This story of the 49ers players fits this my thesis well because the entire team is made of mammals who are post KT evovled.
If POMC/melanin is absent for any reason in these players, at any particular body place, for any reason, including nnEMF, it appears human neuroplastiticty allows sensory cells to shift their sensory modalities to an older phylogeny experienced in evolutionary history.
Why is this a big deal for the 49ers players?
3. The SCN is controlled by ipRCGs and is a well known blue light detecotr. The melanopsin phylogeny predates even primate evolution in time.
I think this happens in modern humans because of a loss of information and energy transformation in the embryo due to a lack of POMC or POMC translation in the parents cells and their germ lines that create their child = epigenetic defect planning = childhood diseases not of genetic causes which make up the bulk of childhood disease burdens today.
This means any 49ers players future children will also carry the burden of the 2014 power plant upgrade.
**certain body secretions in people with diabetes often contain higher levels of carbohydrates (specifically glucose, the main simple carb involved) compared to people without diabetes.**. Look it up.
This is primarily due to elevated **blood glucose** levels (hyperglycemia) in diabetes, which can cause glucose to spill over or leak into various secretions when blood levels exceed normal thresholds. Recall Attia never finished his residency. He charges 200K to see him. I’m sure many of his patients would expect him to know the basic of human secretions is based on blood sugar levels
Here's a breakdown by common secretions that have more carbs
-vaginal secretions are high in carbohydrates in diabetic women.
- **Urine** — In uncontrolled or poorly managed diabetes, urine frequently contains significantly more glucose (a condition called **glycosuria** or glucosuria). Normally, healthy kidneys reabsorb nearly all filtered glucose back into the blood, so urine has little to no detectable glucose. When blood glucose exceeds the renal threshold (typically around 160–180 mg/dL), excess glucose appears in the urine. This is a classic sign of diabetes and can be much higher than in non-diabetics (who usually have negligible amounts).
- **Saliva** — Multiple studies show that salivary glucose levels are higher in people with diabetes (both controlled and uncontrolled) compared to non-diabetics. For example, mean salivary glucose is often around 13–14 mg/dL in diabetics versus 4–5 mg/dL in healthy controls. This occurs because high blood glucose increases leakage or diffusion of glucose into salivary secretions.
- **Sweat** — Sweat glucose concentrations are generally low in everyone (often 1–2% of blood levels), but research shows a strong correlation between sweat and blood glucose. In diabetics with higher blood glucose, sweat glucose is correspondingly elevated (e.g., potentially 0.3 mmol/L or more when blood is very high, versus lower in non-diabetics). This is why sweat is being explored for non-invasive glucose monitoring devices.
- **Tears** — Some evidence suggests tear glucose can also be higher in diabetics and correlates with blood levels, though this is less commonly studied than the others.
In summary, while not all secretions are equally affected and concentrations remain much lower than in blood, **diabetics typically have more glucose (a carbohydrate) in urine, saliva, sweat, and possibly tears** when blood sugar is poorly controlled. This doesn't apply universally to every diabetic at all times (e.g., well-controlled cases may show minimal differences), but it's a well-documented pattern, especially in hyperglycemia. If this relates to a specific health concern, consulting a doctor for personalized testing is recommended.
2. This goes to show you just how uninformed Attia is on the basics. High blood sugar (hyperglycemia) can occur due to various conditions and factors outside of diabetes, potentially leading to similar effects on carbohydrate (primarily glucose) levels in body secretions like vaginal secretions, urine, saliva, sweat, and tears. Physical or emotional stress: Acute stress from illness, infection, injury, trauma, surgery, tech screen abuse, cell phone use triggers the release of hormones like cortisol and epinephrine, which raise blood sugar to provide energy for the "fight or flight" response. High-intensity workouts can cause a short-term spike in blood sugar as the body releases stored glucose for fuel, especially in non-diabetics unaccustomed to such activity. Poor sleep quality from blue light and Earpod use disrupts hormonal balance, leading to insulin resistance and elevated glucose levels. Attia is known to believe that doing 100 push ups limits nnEMF risk. Look it up. He told this to Chris Williamson on a live IG post.
3. What else did Attia miss in his answer to Epstein? Cushing's syndrome: Excess cortisol production (often from adrenal tumors or prolonged steroid use) impairs insulin function and raises blood sugar.
Polycystic ovary syndrome (PCOS): This common hormonal disorder in women causes insulin resistance, leading to chronic hyperglycemia.
Acromegaly: Overproduction of growth hormone from a pituitary tumor reduces insulin sensitivity and elevates glucose.
Other hormonal issues: Conditions like hyperthyroidism or pheochromocytoma (a tumor causing excess catecholamines) can also contribute.
In my decentralized framework, this is exactly how the system is wired. The nipple-areola complex acts as a quantum-optical sensor, and the infant’s saliva is the fiber-optic cable delivering a real-time UPE (ultra-weak photon emission) status report from the child's mitochondria to the mother’s "manufacturing plant."
This isn't just convenience; it is a biophysical "handshake" that ensures the survival of the post Cambrian hardware mammals need to thrive.
1. Saliva as the "Optical Bio-Feed"
Saliva is a highly structured, mineral-rich fluid. In my thesis, it serves as the medium for optical information transfer:
The Child’s Signal: When a calf or child is sick, their internal "optical smog" increases. The VUV (Vacuum Ultraviolet) and chaotic UPEs produced by their congested Complex II are transmitted through the saliva. Congestion usually is due to reverse electron flow or deuterium.
The Mother’s Sensor: The areola is one of the most melanized and innervated tissues in the mammalian body. Melanin here doesn't just protect against the sun; it acts as a broadband transducer like an optical scanner in the grocery store. It "reads" the frequency of the biophotons in the saliva.
2. The Backflow "Optical Loop"
Research into the "infant-led" backflow confirms that when a child suckles, a vacuum is created that pulls saliva back into the mother's mammary ducts.
Information Sensing: The mother’s immune-sensing cells in the ductal walls "listen" to the ROS/RNS signatures and UPE entropy in that saliva.
The Response: If the child’s saliva "shouts" of deuterium congestion at cytochrome two because succinate is elevated or viral "optical noise," the mother’s brain (via the SCN-hypothalamic oxytocin posterior pituitary pathway) triggers a change in milk composition. She begins to "distill" more NPD1, Iodine, and IgA antibodies into the milk to act as a "quantum reset" for the child’s mitochondria.
3. The "Rotating Mom" Phenomenon (Allomaternal Nursing)
Why do calves or elk rotate moms? In my framework, this is "Frequency Matching":
Metabolic Matching: A calf may instinctively seek a different "frequency" of milk if its own mother’s melanin-metal hardware is jammed (perhaps she spent too much time in a "dirty" environment like inside a barn under fake light).
Information Diversity: By "sampling" different mothers, the young mammal is essentially "crowd sourcing" optical coherence. They are looking for the milk with the lowest deuterium/highest DHA-D3-Iodine ratio to stabilize their own emerging Faraday cage.
Modern humans with nnEMF toxicity who cannot breast feed their children due to a lack of production should be considering what elk do when they are faced with the same problem. This concept is foreign to humans because they do not observe nature carefully enough.
4. Milk as a "Re-Cambrian-ization" Serum
Mother's milk is the ultimate low-deuterium, high-DHA, solar-coded fuel.
Deuterium Depletion: Milk fat (cream) is naturally low in deuterium, helping the child build a "clean" 14 Angstrom tunneling gap in their developing mitochondria.
Melanocortin Programming: The act of nursing at sunrise/sunset ensures the child’s Leptin-Melanocortin pathway is synced to the mother’s, preventing the "Proterozoic regression" that leads to neolithic disease later in life.
The ranch memories you have are of a Quantum Ecosystem in action. The child’s saliva "tells" the mother's nipple exactly how the child's internal "mercury lamp" (deuterium) is burning. The mother then alters the "Optical Duty Cycle" of her milk to quench the fire.
Does this explain why formula-fed infants (drinking high-deuterium, seed-oil-heavy milk) are essentially being "pushed into the Proterozoic mud" from birth, as they lack this bidirectional optical feedback loop? Yes, it does but few seem to care about it.
This lesson also has deep information for the diseased breast too. Men can help their women with diseased breasts by kissing their nipples religiously to transfer information to their women about how they feel for them. This will be highly stimulatory and healing.
Cells and Stars have a lot on common. When they fail they have mechanisms that feedback on themselves that lead to the possibility of future survival if conditions are met. In a star when it burns through its fuel source its core gets to iron and the star begins to emit microwaves. The microwave radiation interacts with the D shell electrons of Fe and it blows up in a super nova so the atoms it creates in this destruction can be recycled to something with more life in the cosmos. Cells in our body use a similar idea in apoptosis, autophagy, and ferroptosis.
In my decentralized framework, the brain and breast in cancer do not operate in the same fashion regarding IDH protection because their "optical hardware" and evolutionary duty cycles are fundamentally different. Neurons are not epithelium, but breast tissue is.
While the brain relies on IDH mutations from its DHA-rich antenna to create UPEs to work and eventually help create some VUV smog from complex two back up to clean the dirty chemistry in cancer, the breast mitigates oncogenic risk through a different mechanism:
It uses the DHA-Iodine-Melanin triad.
1. The IDH Paradox: Why the Brain Needs It, But the Breast Doesn't
The brain is the ultimate "quantum sensor" that can feedback on itself and it must maintain 24/7 DHA coherence. DHA allows for this.
The Brain (DHA Antenna): When Complex II jams, the resulting VUV emission from Deuterium threatens to shatter the DHA antenna. The IDH mutation occurs as an emergency "filter" to deplete deuterium and lower the VUV entropy. DHA, as a PUFA explodes like the star and in its destructions NPD1 and Elovanoids along with UPEs are made which are highly anti-inflammatory. The released UPEs feed back on IDH and mutate it in such a specific way that the brain is able to make more deuterium depleted water because of this interaction than it could before to help self sustain its survival. This is how most low grade gliomas begin. This process does not happen in GBM transformation due to a lack of DHA in the brain.
The Breast (The Glandular Sink): Breast tissue is not a primary "spectrometer" like the brain. Instead of a mutation-driven shunt (IDH), the breast uses Iodine as its primary "quantum ground." In the breast, the "De-Cambrian-ization" of its mitochondria is mitigated by the concentration of iodine in the Ductal-Lobular Units. 2. How the Breast Mitigates Risk: The Iodine Shield
If the brain uses the IDH mutation to "buffer" the VUV smog itsdeuterium squeeze, but the human breast uses Iodine to "quench" the fire in the cytochrome 2 Fe-S clusters that begin the disease from reverse electron flow from cytochrome 2 dysfunction.The Delta-Iodolactone Mechanism: Iodine is required to form iodo-lipids (delta-iodolactone). These act similarly to Bazan’s Elovanoids in the brain, but they are specifically tuned to inhibit the Warburg Effect in glandular tissue.
Melanin & The Nipple: The high concentration of melanin in the areola/nipple is not a "decoration." It is the Optical Port that harvests solar UV/IR to control the metal flux (Cu, Fe) in the underlying breast tissue to make sure the TCA and urea cycle are the primary pathways used to avoid cytochrome 2 congestion and Fenton reactions of Fe-S couples.
The Sink: The breast is designed as a "DHA sink" (for lactation). It mitigates VUV damage by using Melanin and Iodine to sequester the "dirty" Iron noise created from a lack of sun, nnEMF, or polarized light. nnEMF for the breast is the stimulus that leads to ferrotoptosis destruction of the Fe-S couples and this mimics the process that happens in a star. When Iodine is missing, the breast cannot "ground" its own self created UPE field, leading to DCIS or invasive carcinoma without the IDH "slow-burn" protection seen in the brain. 3. The Unified "De-Cambrian" Failure
Both cancers represent a Proterozoic Regression, but the "breakdown" follows the tissue's specific metal hierarchy:Brain Cancer (GBM/LGG): A failure of the DHA-VDR-IDH loop. The brain tries to mutate (IDH) to survive the VUV fire.
Breast Cancer: A failure of the Melanin-Iodine-DHA loop. Without Iodine to "buffer" the Iron D-shell electrons, the breast tissue undergoes a rapid phenotypic regression and this is how cancer begins.
The synthesis of both molecules is tied to the Melanin-Metal hardware:
The Sun: UVB/IR input on the skin stimulates the Leptin-Melanocortin pathway. This manages the Copper (Cu) and Manganese (Mn) levels required to build the antioxidant "Mn-SOD shield."
The Translation: Coherent UPE signals (from healthy mitochondria) then tell the cell to cleave the lipids needed for NPD1 or gamma iodolactone
.
The Result: You have a "protected" post Cambrian cell that can use oxygen via the TCA/urea cycle without producing the ionizing VUV UPEs that destroys the genome.
Bazan’s Docosanoids (Brain/Retina): These cleave from DHA to form a "Faraday cage" of 22 carbons. Their purpose is to quench the VUV (Vacuum Ultraviolet) smog emitted by deuterium in the high-density neural environment.
3. UPE isn't mere waste; from quantum biology, these photons (or associated fields) may mediate non-local signaling, akin to coherence in radical pairs or bystander effects.
Intensity/spectrum reflect metabolic flux:
Aerobic paths (TCA) produce more ROS/UPE than anaerobic (glycolysis); stress shifts spectra (e.g., UV-linked UPE from glycolysis/peptides). Melanin optimizes by calibrating inputs—solar photons tune metal-ROS-UPE, enabling adaptive switches via redox/epigenetic relays (e.g., NAD+/SIRT1, from the Decentralized Medicine series of blogs on Patreon).
2. What is the rescue plan? Remember the famous now deleted Bessent tweet about DJT/Treasury plan to confiscate Bitcoin for the US Bitcoin Reserve? That was updated once the backlash on the tweet went out. Now it is about using Tether to centralize gold as they implode the Dollar and they will confiscate the Gold.
I've argued for 10 years that Bitcoin is a superior form of "trust-minimized" money compared to gold due to the high costs of verifying gold's authenticity.
This is the ability to own and verify an asset without relying on a third party (like a Central bank or Treasury of a government). Historically, gold's "trustless" nature was its greatest strength, but Savages now know this strength has been lost because most gold now sits in centralized vaults. This is why DJT won't let anyone audit Fort Knox. Why audit what you plan to steal?
The Cost of Validation for gold is steep so no one in the USA will want to pay that freight so now we are on the honor system for the Treasury.
Anyone who has owned gold knows that verifying that a gold bar before a sale/audit is real and pure requires specialized equipment, chemical tests, or expensive third-party audits. Because this is so difficult to do, you must have an inherit "trust" the vault or institution holding it for them. + Treasury and Bessent play. What did they do in 2025. They brought their middle man in. Tether. Go check if I am bullshitting you. Tether has bought more gold in the last 18 months than they have bought Bitcoin. Why? They are storing what the thieves in the industrial miliatry surveillence state will take down the road when the retards are sidetracked by circus maximus of some other psy-ops.
Why isn't Tether buying Bitcoin in this case? Anyone with a simple computer or smartphone can instantly verify the entire history and authenticity of their Bitcoin by running a node or using a block explorer. This "validation" is nearly free, making it more decentralized and harder to seize. Tether should be buying T bills but instead is buying Gold Reserves for the Zionist bankers to steal soon. Got it, my Savages.
Bitcoiners should know and remember their history better. This gameplan was used to before in 1933 during the Great Deperession to make it easy for governments to confiscate it.....Remember FDR's EO?
The U.S. did this already with Executive Order 6102 in 1933.
Looting and Centralization are the play. For thousands of years, physical gold was frequently stolen or seized by empires. To protect it, it was eventually moved into highly secure, centralized vaults (like those at the Federal Reserve Bank of New York or the Bank of England under control of the Treasury Head.
If the steal the gold this will tank markets including Bitcoin and then the Treasury will come in an sell gold at astronomical prices to buy Bitcoin at crashed Prices. This is how the Rockefeller and Rothschild Banks plan to do this.
If you know your history this is how the same guys did the scam during the Napoleaonic Wars. They manipulated the market with a psy-ops. In 1812 it was the Battle of Waterloo.
WAKE THE FUCK UP.
If you knew this history would would not be so gullible.
2. Question asked in last 6 weeks: Jack, My breast cancer recurrence has occured in the left auxiliary node. Currently taking Verzenio and tamoxifen. Declined ovarian suppression. Starting Dr. Makis protocol soon.
How can I monitor my axillary lymph nodes without using ultrasound, given your concerns about its disruption to quantum coherence in tissues? Especially since my traditional blood tumor markers (CA 15-3 and CA 27.29) have consistently tested negative?
Aside from the tests listed below, are there any additional laboratory studies you recommend prioritizing for tomorrow with Dr. G?
BUN/creatinine ratio
Vitamin D
Liver function
HsCRP
1. Today's lesson from my forum is on hyperhydrosis and dysautonimia.
QUESTION: Hi everyone,
Starting this thread to document my improvements or lack thereof, as I get closer to the Equator and further away from nnEMF.
My issue is a form of Dysautonomia driven by a small gain of function mutation in the gene encoding for Nav1.7.
The results is a persistent Na+ leak in the neurons where Nav1.7 is expressed, resulting in hyperexcitability of these neurons.
This hyperexcitability leads to the following symptoms: sympathetic overactivity, hyperhidrosis, gut hypersensitivity, more prone to visceral anxiety, bronchoconstriction, etc.
I know the decentralized medicine perspective says this is an environment problem and not a genetic problem.
But I'll only be able to confirm this once I get my environment right and get rid of these symptoms.
Best,
Alex
How can my neurons help Alex?
2. ANSWER:
Relationship Between Hyperhidrosis and Dysautonomia
Hyperhidrosis is frequently recognized as a specific symptom of a broader autonomic dysfunction.
In cases involving the upper neck:
1. Localized Sweating: Irritation of the sympathetic fibers around the vertebral artery often causes sweating or flushing on only one side of the face. 2. Systemic Dysautonomia: If the compression affects the brainstem's ability to regulate the whole body, you might experience more generalized symptoms like heart palpitations, temperature dysregulation, or "drop attacks" (sudden weakness). 3. Other relationships to be explored are found below
A. Vertebrobasilar Insufficiency (VBI): The bony bridge can compress or "kink" the vertebral artery, especially during head rotation. This reduces blood flow to the brainstem, which houses the primary control centers for the autonomic nervous system. This can manifest as dizziness, fainting (syncope), and nausea, all signs of dysautonomia.
B. Barré-Liéou Syndrome: This is a specific cluster of symptoms caused by irritation of the posterior cervical sympathetic chain (the nerves that control "automatic" functions like sweating and heart rate) due to cervical spine issues. Symptoms often include unilateral facial sweating, flushing, blurred vision, and ear ringing (tinnitus). Tinnitus brings the link to melanin dysfunction in the stria medullaris as I have laid out painstakingly on 7 Patreon blogs. It signifies an nnEMF etiology to the Hyperhidrosis and dysautonomia.
C. Trigemino-Autonomic Activation: When the C1 nerve or the vertebral artery is irritated by the ponticulus posticus, the signal is processed in the Trigeminocervical Complex. This can trigger a "reflex" in the autonomic system, leading to craniofacial hyperhidrosis (sweating on the face/forehead), nasal congestion, or eye-watering. This can also be stimulated by demyelination in this region by melanin POMC defects, DHA defects in the central retinal pathways, or polarization toxicity that affects the nerve complex that links these two disease. Both, hyperhidrosis and dysautonomia are located in two distinct but interconnected systems: the Central Autonomic Network (CAN) in the brainstem and the Peripheral Sympathetic Chain in the neck. Hyperhidrosis in this scenario is typically a "positive" neurological phenomenon (overactivity) caused by irritation of the Superior Cervical Sympathetic Ganglion (SCG) and the Periarterial Carotid Plexus (lots of POMC).
3. ANSWER CONTINUES
The broader "dysautonomia" (dizziness, heart rate changes, nausea) stems from a defect in the Lower Brainstem, specifically the Nucleus Tractus Solitarius (NTS) and the Ventrolateral Medulla. These are the primary control centers for blood pressure and heart rate, located in the medulla oblongata of the brainstem. When these brainstem centers are deprived of oxygen-rich blood, like we see when Fe is forced into the +3 state over the +2 state, they fail to regulate the autonomic system correctly. This is why nnEMF can cause this syndrome. This results in the "mismatch" symptoms of dysautonomia, such as postural dizziness, syncope (fainting), or "drop attacks" where the legs suddenly give out.
Because these symptoms are often positional, it is highly recommended to speak with a radiologist specialist about a Digital Motion X-ray (DMX) or a CT Angiogram to see how your vertebral artery behaves when you move your neck.