2. The Raman effect is the change in the wavelength of light that occurs when a light beam is deflected by molecules. It was named after Sir Chandrasekhara Venkata Raman who was born on this day, 7 November 1888.
The Raman effect is used to analyze different types of material. This effect has massive implications in biology that have gone unnoticed by the mainstream for over 130 years. The mechanism was the basis of what MKULTRA evovled to study after the use of drugs failed.
This effect is seen in all things. You can see it in chickens and humans. youtube.com/watch?app=desk…
3. Elon Musk made a joke this AM on "X", but the joke is on him and on the public. Blue voting regions corresponds to were Raman scattering science is being used through screens and satellites by the Industrial military complex. It is most useful relationship to gain control of people as laid out in the MKULTRA program. It evovled from MKULTRA to SRI and now resides in the Brain Health Iniatives offshore in Centers of Excellence. In USA cities this is where CTIA and the FCC made sure nnEMF towers are placed closer to people and can be used to control neurons is stronger via the inverse square law. @JonesDanny @NicoleShanahan
Few people really understand that this map mimics where tower density is located in the USA. If you live inside a city you'll understand why those people comply with government beliefs.
4. Sleep disturbances and sleep/wake rhythms are major problem seen in humans who live in cities who have mental disorders. These disturbances are observed during the different phases of the disease and are major symptoms of mood episodes and belong to the diagnostic criteria for depression, hypomania, and mania.
In addition, these anomalies are also found during the euthymic phases of this disease. Indeed, patients suffering from BD would be more likely to present a more evening chronotype and a more languid and rigid circadian type than healthy subjects as well as a decrease in the efficiency of their sleep, an increase in sleep duration, an increased sleep latency and a prolongation of the duration of awakenings after the onset of sleep. These disturbances in sleep and wake/sleep rhythms are associated, among other things, with more frequent relapses, an alteration in the quality of life, and cognitive disorders.
5. Few centralized MDs & psychiatrists today are trained to even know full spectrum sunlight lowers cholesterol naturally. Even fewer realize that nnEMF from screens, phones, satellites raise blood glucose and insulin and this ruins how POMC is cleaved. This controls how we sleep and how we behave. It makes us more or less controllable based upon the electromagnetic tuning of our nervous systems by the devices. That was the purpose of MKULTRA at its core.
Today, even fewer realize sunlight is the best treatment option for sleep and mental illness because the government is deathly afraid that they will lose control of the populace to obey and consume and take on debt and listen to Manchurian candidates who support their agendas braoadcast on TV, radio, and podcasts.
Most of them have no clue that sunlight is the EMF where the human system was built by Mother Nature to get rid of deuterium to keep fidelity high in the SCN and other parts of the brain that allow us to reason and think critically. Blue light at night is an additive effect that makes the process deadly in government programming and in most mental diseases we today. We see this reflection in government appointed leadership.
This is why there are several formats or phenotypes of disease as you saw in the video of this blog that mimics heteroplasmy in the system. patreon.com/posts/quantum-…
6. These are the results below.
7. What type of voter do you create when you put them in terrestrial sunlight and do not geo-engineer the skys above them? You create a threat to the criminals who were in Washington DC since JFK was killed by them.
8. TYING IT BACK TO MY THESIS OF MY BLOG SERIES: POMC
The adrenal medulla of mammals was born under the light stress of the KT event. This is why I wrote the adrenal fatigue blog years ago but no one saw things back then like they do now. I told the implications of that Huberman/Rubin podcast were VAST. THE VOTING MAP disorder posted by Elon Musk is one of these VAST effects.
Man's five senses can capture the vastness and the immensity of our cosmos and POMC is the paintbrush that allows it. POMC is the paint that goes on the canvas, your brain. POMC is a color palate that humans use to paint their minds. In some ways, that palate confines us to the limited real estate of the sensory organs in our brains to understand all the complexity of the universe. All 5 senses tract directly to the thalamus of humans which surrounds the 3rd ventricle of their brains. But there is wisdom in being connected to nature in this fashion. Yet, few see the artistic symmetry of confinement. I am trying to explain this art to you now every day, in every word I write in every one of these blogs. It is time for you to LEVER UP your knowledge.
THE LEVER-UP LESSON: The adrenal cortex synthesizes three main groups of hormones (glucocorticoids, mineralocorticoids, and adrenal androgens) (Auchus and Miller, 2001). The homeostasis of glucocorticoidsis regulated by a feedback mechanism CONTROLLED BY POMC gene translation via solar light and temperature sensors (non-visual photoreceptors) in the skin, eye, and autonomic nervous systems that are relayed to and through the hypothalamic POMC centers in many neuron tracts and in the circumventricular organs (water networks in the ventricular system of the brain) by means of corticotropin-releasing hormone (CRH), the pituitary gland by ACTH, and the adrenal cortex by cortisol (Koch, 2004).
9. In chemistry and physics, Raman scattering or the Raman effect is the inelastic scattering of photons by matter, meaning that there is both an exchange of energy and a change in the light's direction.
The Raman effect is a phenomenon that occurs when light interacts with matter in a cell, it causes a change in the wavelength of the light. That change is used to signal. When light interacts with a molecule, some of the light scatters off with a different energy level. This is because the vibrational modes of the molecule change the energy of the scattered light. The Raman effect can provide information about the chemical bonds, molecular structure, and vibrational dynamics of a substance. Raman scattering can also be used to create high resolution images of atoms, DNA, and single molecules.
Raman scattering is a type of scattering that occurs as part of the Raman effect. In Raman scattering, the scattered light has a different energy level than the incident light. In Rayleigh scattering, the scattered light has the same energy as the incident light. Rayleigh scattering is why our sky appears blue. Rest assured it is not blue. That is how it appears to our retina. Our brain however is not fooled because of the FM antenna system in out thalmus that responds to the Schumann frequency of Earth.
10. You do not know what you do not know until Mother Nature informs you and your SCN and thalamus encode it into your mind and being.
11. The thalamus is where the alpha wave of the brain begins. The brain uses a range of frequency patterns monitored by the EEG system in our neurosurgical clinics. The frequency range of the EEG rhythms coincides with the frequency range of the Schumann Resonance signal (0–45Hz).
The alpha wave is identical to the frequency most commonly linked with Schumann's resonance on Earth. The normal brain has developed an ELF oscillating ion system, primarily using calcium ions (above), to control neurotransmitter release. The release is awry in BD. Dr. Russ Adey at UCLA established this in the 1970s. Adey's work is cited below. The human brain and its optical clock lattice in the SCN are now well-established in the literature.
Blackman's work on calcium ion resonance frequencies was cited multiple times in Becker's books and my early blogs on the non-ionizing effects of nnEMF and neurological compromise. Blackman's research also cited below, has taught decentralized MDs that external electromagnetic ELF signals induce altered neuron calcium ion effluxes in mitochondria of brain tissue.
12. The receivers used by Mother Nature mimic an FM radio in your car. Yes, the human brain has a built-in FM radio system. I was not joking above. In the human brain, there is included a phase-locked loop system, described by Ahissar et al. This paper is cited below.
A phase-locked loop system = modern FM radio receivers in your car.
In the human brain, the FM radio receiver interacts with the Schumann Resonance signal. The phase-locked loop is a very useful circuit block that is widely used in radio frequency or wireless applications in tech gear. Given its usefulness, the phase-locked loop or PLL is found in many wireless, radio, and general electronic items from mobile phones to broadcast radios, televisions to Wi-Fi routers, walkie-talkie radios to professional communications systems, and much more.
Mother Nature built this system over 3 billion years ago in the brains of living systems to inform cells of the seasonal connection between the sun and Earth so this data could be useful for seasonal biological changes in living things. In bipolar disorder, this system is awry when it is encumbered by too much mass in the receivers of the FM radio. MKULTRA found how to disturb this FIDELITY to control your behavior.
The circadian activity generated in the SCN needs to be transmitted to the rest of the brain and henceforth to the rest of the body via non-optical signaling to stay well. In Bipolar Disorder this is impossible because the SCN is where the main deuterium defect lies.
That EMF receiver is not receptive to Schumann's information. Coherent connection ruins the fidelity of the system. Most of the centralized science right now believes it is through direct wiring tracts. I do not. I think it happens via the hydrogen bonding network in the circumventricular organs filled with CSF water. These areas in your brain have no blood-brain barrier by design.
13. The human brain SCN contains the key mechanism to having a strong diurnal pattern that assists the sun to maintain the circadian rhythm. The Schumann Resonance signal continuously synchronizes the brain wave ELF patterns in a set range of grouped frequencies that begin in the thalamus that surrounds the 3rd ventricle of the brain. The ventricular system also acts as a resonant cavity on Earth to receive these signals.
The hydrogen bonding network in CSF is another FM-like receiver in the phased locked loop communication system mentioned above. This stabilizes the brain's electromagnetic system of communication and its fidelity has enabled the evolution of intelligence and consciousness with an ability to provide stable thinking to make predictions. This system has evolved to the point in humans where this complex understanding of the biophysical environment interacting with the human brain can be reasoned, understood, and appreciated.
14. Water makes up 99% of molecules in every cell and it fills the ventricles of our brain. Water is a very small molecule that has more hydrogen bonds in it than any other compound. Liquid water contains the densest hydrogen bonding of any solvent, with almost as many hydrogen bonds as there are covalent bonds and hydrogen bonds in its structure found anywhere on Earth. These two bonding networks are the binary code in water. Just as a computer can use a 1 and 0 to create digital information on the internet, hydrogen bonds create the internet in your cells. Shannon taught us the information content of any kind of message could be measured in binary digits or just bits. This was the basis of the Kruse for my Dummies talk I did early this year to get my tribe ready to understand what I dropped in the Danny Jones podast. @JonesDanny
Water's hydrogen bond network changes at a pico and femtosecond level in any environment. Inside a cell, its atomic arrangement is controlled by electrostatic forces in a cell created by the redox power of the mitochondria in that cell. These hydrogen bonds can rapidly rearrange in response to, light frequencies, charge density, and changing conditions and environments (for example, solutes like K+ in a cell). This is how our ventricles tell seasons in us. It is also how the government changes signals in your brain use light frequency changes in screens and in towers around you to GET TUNABLE RESULTS. Elon showed you his map again, but clearly has no idea how his work is going to be stolen and used like TESLA's was in 1943 by the CIA.
It is also how neurosurgeons should use MRIs differently to diagnose clock disorders in their patients. I know I do it every day. Normal pressure hydrocephalus for me is diagnostic of a brain filled with deuterium and a completely disordered clock system. These people are walking time bombs for intracranial clots and neurodegeneration. POMC is degraded massively in these patients. When you add bioweapons to this mix you create a targeted weapon that can penetrate the iron dome system of the SCN and human thalamus.
When the FM system is bad in the neocortex, brainstem, and thoracic spinal thalamic tract you cannot tell seasons and you become very compliant and controllable remotely using light frequencies. That is the result of MKULTRA.
15. Neuropsin is a 380 nm light sensor that the locus ceruleus needs to function well and for you to remain a critical thinker.
Without this non-visual photoreceptor system operational, this opens the BBB and the gut barriers. Now you see why Nature put neuropsin in your eye and skin. We see this in most of the psychiatric cases induced by MKULTRA and in TBI cases due to the light stress response. Now you can see why really the brain-gut barrier is linked. Usually, there is a lack of melanin in the DLF of the brainstem and/or the locus ceruleus to create the aura of brain-gut barrier when in reality what links the two is a lack of UV light to stimulate POMC in both hypothalamic pathways and melanin is degraded leading to many disease phenotypes. MKULTRA uncovered all this for the CIA/FBI in 1953-2010.
Each somite in the spinal cord also has POMC genes in them ready to be activated. They are derived from the neural crest in this part of the body. For the gut, this is linked to the celiac ganglion which comes from T5 -T11 thoracic nerves. So thoracic level solar exposure is key to renovating gut-level melanin. It is counterintuitive until you see it all laid out in front of you. A lot of this deep science would have been in the Vermont 2019 video I was going to give 4 years ago.
16. What I am explaining to you now is where in the topological map of the human brain and Elon's map both link to the POMC deficits in human nervous systems is located leads to the phenotype of the disease or bad thinking we see in our clinics or in our voting districts. Patients with this disorder intuitively know they need more sun but the government blocks it by dermatology and ophtalmology decree. Or they allow Gates to block the sun and support geo-engineering in your city zip code to make you an obedient idiot. How they go about it is often incorrect as you see in the cite below.
Understanding the human eye and retina and linking it to entropy in a cell was the only quantum leap I made to understand this concept. The flow of entropy is why I made this prediction back in 2010. All molecular clocks are flow meters for entropy. I knew the SCN had to be doing something unusual with the retina and the brain during sleep. The SCN appears to be a perpetual motion machine built into the brain that uses Raman scattering to optimize us. Feynman wrote a paper in 1982 stating he believed a quantum computer could simulate physics if it used a time crystal.
The SCN is a small computer in your eye that is simulating the physics of the environment between the sun and Earth to make the best predictions for cells in tissues. Today your government has learned how to ruin the fidelity of that time crystal to control how you think and behave. It is not working well because the mass inside of it put there by the light you allow ruins its signaling. Adding mass back to the water networks, or using certain drugs is how they control those who have gone truly made from this program. You know the Charles Mansons, Rachel Madows, Joy Reids or the P. diddy's of the world. They are all created by the criminals in DC.
The problem is the system fidelity operates at quantum mechanical precision with respect to mass and this is why results are so uneven in patients with this disease. Just look at who changed the light around you........to see what you've been missing. MKULTRA is now present in the human environment at global scale because of government policies. Guess why?
Adey W. R. Electromagnetic fields and the essence of living systems. In: J. Bach Anderson (ed). Modern Radio Science. Oxford University Press; 1990. p. 1–37.
Ahissar, E., Haidarliu, S., Zacksenhouse, M., 1997. Decoding temporally encoded sensory input by cortical oscillations and thalamic phase comparators. Proc. Nat. Acad. Sci. USA 94, 11633–11638.
Blackman C. F. ELF effects on calcium homeostasis. In: B. W. Wilson, R. G. Stevens, L. E. Anderson (eds). Extremely low-frequency electromagnetic fields: The question of cancer. Columbus: Publ. Battelle Press, 1990: 187–208.
Cherry N. J. Schumann Resonances, a plausible biophysical mechanism for the human health effects of Solar/ Geomagnetic Activity. Nat Hazards 2002; 26: 279–331.
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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.