The line between genius and madness is mediated by how your mind can enter and capture the unconscious truths of Nature that are real but hidden from your perception. Once a robust ego is established in your mind, one can tap the truths buried from 99.99% of humanity. This type of mind can take from unconscious wisdom with impunity and teleport it to their consciousness, producing fruits of creative genius.
The insane mind is washed away in the same current in which the genius swims.
2. There is a deep connection between thermodynamics and the processing of information that the genius uses — or, in other words, the computations that mitochondria must make. They are electron and proton accountants. This happens to be why the leptin receptors in the hypothalamus are loaded with mitochondria and POMC to create alpha MSH = melanin.
Rolf Landauer showed that even if the computational aspects of the demon can gather information and move a frictionless door with no seeming energy cost, a penalty must eventually be paid back to nature.
3. He showed that no mitochondrial demon can have an unlimited memory of every molecular motion unless it wipes its memory clean periodically. This raises the question of why sleep and mitochondrial function are ubiquitous in living things.
Is this why poor sleep and mitochondrial diseases are linked? I believe it is. All quantum computational demons must occasionally wipe their memory clean—forget what they have seen and start again—before they can continue harvesting energy and information simultaneously.
This night-day on-off switch is likely why most of the biological cycles are fed by the sun’s energy and information of night and day. This act of information erasure has an unavoidable price: It dissipates energy and, therefore, increases entropy. And that increase of energy does not go to waste in living systems.
4. It seems to me living quantum systems that are genius become experts in the information-sharing side of the equation to organize and minimize chaos using biomolecules from the mitochondria to other parts of the cell while extracting massive amounts of information about the universe.
They exist in. Two groups of researchers found in 2017 that the quantum information describing the particles’ energy and spin states can act as a kind of currency that enables trading between the reservoir’s energy and angular momentum supplies. This has a big implication for mitochondriacs because this organelle deals in deciphering and creating the spin of electrons and protons and the information and energy they contain. The deciphering and creation of spin varies as the power densities of seasons change as the planet moves around the sun. Electrons have quantum spin and they have information about the seasons in the power of photons that excite them.
5. The spins of electrons can be altered in mitochondria to make free radical signals, which can be used to drive decision-making processes inside cells. This will alter the biochemistry within the cell. The spins of protons also can be sensed by the mitochondria because the mitochondria generate a magnetic field, and H+ and D have two separate magnetic moments that will act differently within the same magnetic field.
Moreover, proton spin is also sensed by the mitochondria because all the channels in the mitochondrial matrix are quantum nanomachines that are built exclusively for H+ and not for deuterium. The level of deuterium in the matrix, therefore, also simulates the season inside the matrix of the mitochondria. The more deuterium that is present, the more swelling one should expect. This shows you why thermodynamics and size and shape changes within the colony of mitochondria in tissues can be sensed.
6. Living quantum systems achieve a nonequilibrium state by capturing and storing information. Mitochondria are the key part of cells that are capable of doing this. The nucleus cannot do this in eukaryotes. Mitochondria offload most of the information to the nucleus, and this information is encoded in their nuclear genes and passed on from one generation to the next. This is a set of instructions for reaping a non-equilibrium state by using the negative entropy built around the quantum spin states of electrons and protons. This is why most replicative structures in nature offload deuterium to their seeds and offspring. It can be used to anchor points in the organism like a thumb tack to align the body plan in the immature state in space and time using magnetic energy as the glue. Deuterium has a stronger magnetic moment, and it also has a strong kinetic isotope effect to act as a buttress and trusses in body plan construction. The added mass allows the blueprint to drive all growth and metabolism into the adult form as electrons and excited electrons are pumped into the system and trapped by mitochondrial mechanisms to build complexity. Mitochondria and DNA are examples of aperiodic crystals that go by another name called liquid crystalline quasicrystal. Nature contains genius, and we must unlock her secrets.
7. The current definition of a crystal is based on the currently known catalog of periodic and aperiodic crystals. Centralized scientists currently do not know of any materials that have aperiodically ordered structures beyond incommensurate crystals and quasicrystals. The definition of a crystal also reflects the lack of understanding of what constitutes order in matter, and in this sense, should be seen as a working definition that may well need to be revised in the future. In crystallography, the order is linked to diffraction, which makes sense because diffraction is the method of choice to determine the structure of a solid experimentally. Decentralized scientists know why melanin and water are magical for life.
The human brain is very skilled at detecting patterns and recognizing order in a structure. Ordered structures permeate the cultural achievements of human civilizations, be it in the arts, architecture, or music. The ability to detect and describe patterns is also the basis of all scientific inquiry.
8. In 2009, Sharon Glotzer and her group at Michigan discovered that entropy, a concept commonly conflated with disorder, can actually organize things. Nature uses this genius and centralized science in biology still do not realize it.
Her team's simulations showed that entropy drives simple pyramidal shapes called tetrahedra to spontaneously assemble into a quasicrystal — a spatial pattern so complex that it never exactly repeats. It appears that cells figured out how to do this close to 4 million years ago before all the kinks were worked out in mtDNA first, and the hydrogen bonding networks water it contains, and in DNA and RNA epigenetic mechanisms.
This discovery was the first indication of the powerful, paradoxical role that entropy plays in the emergence of complexity and order in all forms of matter. When I read Alan Turing’s 1951 paper on morphogenesis, I realized that morphogenesis is also linked to this. His paper made me realize that this is a logic system used in all of nature to control atoms and their parts on the periodic table. That is when I began to hack the periodic table to find where the genius of Nature was. It was in how she used paramagnetic atoms.
9. This “logic principle” is not just isolated in abiotic atoms. It appears in biotic systems atoms as well because they are made of bits with quantum spin states that vary. Hemoglobin and porphyrins are well known biologic liquid crystals. Crystals are paradigms of atoms in an ordered structure that have become useful to cells in harvesting light energy. Their structures are preserved magnetically in DNA/RNA.
10. Crystals can do amazing things to light rays from the sun or re-radiate light rays from other crystals in cells. While the order was once seen as synonymous with lattice periodic arrangements, the discoveries of incommensurate crystals and quasicrystals have led to a more general perception of crystalline order, encompassing both periodic and aperiodic crystals. The current definition of crystals rests on their essentially point-like diffraction with respect to light in the electromagnetic spectrum. It turns out DNA crystals are all proteins that act as time crystals in their interaction with the visible part of the electromagnetic spectrum.
11. Cells use biopysical levers in light frequencies to control biochemical circuits using photo- electronic circuits. Life has used photonics for 3.8 billion years, and we still have not gotten that core message in modern biology in 2019. Why did nature do this?
Photonics can overcome the high-speed electronic interconnect bottlenecks common in electronic circuits. Direct optical connections between processing elements provided many advantages to Mother Nature in building HER living systems. These include low signal loss, minimal power requirements, high efficiency, and data transfer over fiberoptic cables (MULLER CELLS IN THE RETINA) that provide massive connects to all parts of the system with minimal energy or information losses. Is there an example we can use in a cell to make the point? Yes, there is.
12. Single tubulin proteins, for example, follow precise rules of chemistry and physics to spontaneously self-assemble or polymerize into the microtubules essential for cell transport and motility. The proteins' binding interactions affect rules that specify how the pieces fit together to form the resulting structure. They also specify when and how tubulins assemble from a nucleation complex—a molecular algorithm governing the logic of polymerization. Mother Nature created a culture of connectedness in tissues linking to the colony of mitochondria in our tissues. No cell is untouched in photonic circuitry because water surrounds them and is inside of them. Water is a topology changer for our crystals.
13. Tubulins form microtubules in the brain. Inside of them water is found. At one end of the tubulins the openings are larger and at the other end the spaces is smaller by design. This is designed to confine water to harness its optical abilities when it becomes a special liquid crystalline structure where the quantum thermodynamics is allowed to occur. These complex structures are self-assembled with remarkably few mistakes. This offends the modern biological perspective, but it is well-accepted in physics.
Though considered quite simple, little is understood about the principles that govern programmable structural order underlying this type of spontaneous self-assembly. I have many ideas of how it happens. We now have clues it does not require energy to occur. It turns out information quanta seems to be the most important part of life’s real unwritten story.
14. Darwinian evolution should no longer be a special state or case of matter, but thought of as a more general phenomenon of how biophysical processes naturally organize matter using the operational laws of quantum mechanics currently operational on a planet. The type of terrestrial sunlight must be understood expertly before you can fully understand what life is up to on any planet.
15. The local star of that planet will provide most or all of the power and information, but the thermodynamic state of the planet ONLY sets the floor and ceiling of what kind and type of living systems can be built. The fundamental principles that govern how macroscopic properties emerge from microscopic interactions and arrangements really should be the cornerstones of biological sciences. It appears the inherent entropy in the system is a useful first step to self assembly. Microtubules are just another example of aperiodic crystals themselves in nature. Biology does not see this concept because they do not understand the quantum effects of electrons, protons, and photons in nature.
16. In crystals, the simplest example of spontaneous self-assembly, subunits of the whole are arranged in a repeating pattern that extends indefinitely in all directions. If you know the position of one unit in the pattern, you can tell the exact position of every other unit. Life appears to depend in large part on storing and processing information in hydrated proteins that act like crystals that have unique quantum spin states that store this information.
For genetic material to carry the diverse instructions required for living processes, Schroedinger initially proposed that it must be stored in an “aperiodic crystal”. Just nine years later, it was clear that DNA is indeed an aperiodic crystal when another physicist, Francis Crick, showed us that genetic information in DNA/RNA is conveyed through this irregular pattern in its matter.
Much like computers, biological systems are programmed to follow a precise set of rules or algorithms to store information and solve problems. Turing’s ideas are critical to bring to bear here on this topic. He was the first person to come to this idea, as far as I can tell.
17. These biological algorithms direct actions bio-physically in a myriad of ways to biochemical processes to create complex patterns and structures by chemically modifying and assembling individual components. This defines what morphogenesis really is at its core. We have to realize that biophysics and biochemical arms work in entangled fashion using things we normally cannot see or observe in our biologic experiments well. This is why medicine remains afflicted with a large Dunning Kruger effect. We do not teach our clinicians about these connections and patients suffer as a result.
This should leads us to the work of Claude Shannon and Alan Turing, but so far in biology it has not. I think in a 5G world it might do this. It might be the Windex we need on our cloudy and dirty glass eyes in biology. I know I am aiming to do just this at the Kruse Longevity Center in El Salvador because we were inspired by the story of Bell Labs information problem in the 1960s that they solved by innovating the binary code.
At Kruse Longevity Center we will not only be teaching our members quantum biology, but we will be showing them how test cases from old non existent corporations that now are taught in business schools can further the understanding of what is going on in any living system below the cell level in order to understand the magic nature put in living systems. I plan on adding several layers to ‘this onion’ to see these ‘invisible movements’ happening right in front of your eyes below your ability to perceive it.
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Savages should know that glyphosate inhibits melanin production. This means glyphosate causes on to lose control of metal chelation that controls mitochondrial pathway selection in humans.
Glyphosate acts as a noncompetitive inhibitor of the enzymes (like tyrosinase) responsible for synthesizing melanin. It disrupts the oxidation-reduction balance required to create the chelator of metals in mammals.
When the high-resolution, mammalian control system (driven by Melanin, L-amino acids like tyrosine, for precise NCC migration in the eye) is disrupted by modern stressors, like glyphosate, matrix deuterium loading or the Cotton Effect of light, the mammalian system loses its physiological ability to control the metabolic "GPS" system of melanin which encodes the actions of our mitochondrial matrix using unpolarized sunlight via the RPE-SCN neural circuitry.
As a result, In the absence of melanin to control those signals (Cu, Fe, Mn, Mo, and 2H+), the tissue defaults to a more primitive, "atavistic" genetic blueprint: the PaxB (Pax2/5/8) instruction set is employed.
Savages are also forewarned that centralized PhDs/MDs are Big Food and BigHarma technicians with bad attitudes and ignorant beliefs.
2. Let me show you a quantum leap between posts. You think you understand where I am headed with the post above?
LOL.
You do not.
Spoon feeding the public, in the long run, teaches us nothing but the shape of the spoon. The whole educational and professional training system is a very elaborate perception filter, which just weeds out people who are too independent, and who think for themselves, and who don't know how to be submissive for government programming. Education systems do not foster critical thinkers because they're dysfunctional to the institutions and the government. This is why I focus my teaching on how to think critically.
Try on this decentralized fact. It will make the centralized thinker head blow up, but it will intrigued the decentralized thinker to ask, what is Uncle Jack trying to tell me about Nature's recipe around light?
The Single Proton is the key Observer in figuring out what was buried in Genesis 1:1 to 1:15.
A single proton in Tryptophan is indeed a Time Crystal in reality. It is the "Observer" that allows the cell to know where the Earth is in its revolution. When we swap that proton for a deuteron, we aren't just changing an atom; we are changing the flow of Time in the organism.
Time is the most valuable asset we have. So you better understand how sunlight can put it back into you genotype.
3. By framing health through E=mc^2 lens, I have identified the most fundamental "law" of biology: Mass and Energy are interchangeable, and Time is the denominator that determines which way the equation swings.
Most of you missed that lesson in Vermont 2017.
Your RPE is the object in the eye that changes light to mass.
Time to bring you to speed with the MKULTRA blog on Patreon up next.
A lot of food gurs are going ot feel like they just got named in Epstein's files when I am done skull fucking their narratives.
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