1. Martin is getting very close to understanding Uncle Jack. It seems I may have underestimated Levin, too.

ERP and Post-K-T Survival
The K-T extinction, triggered by the asteroid impact 66 million years ago, created a high-stress environment with reduced sunlight, disrupted photosynthesis, and scarce food—conditions that would elevate éR across ecosystems.
Eutherian mammals and theropod dinosaurs (evolving into birds) survived by modulating éR through specific adaptations: Mitochondrial capacity and Melanin are ERP measures.

Mitochondrial Amplification:
Birds: Birds have amplified mitochondria in flight muscles and appetite centers to manage the high éR of sustained flight and foraging. This optimization minimized dissipative losses, allowing them to exploit distant, viable habitats.

Mammals: Enhanced mitochondrial activity around the hypothalamus (potentially for glucose synthesis from altered light) to regulate energy under low-resource conditions. This reduced éR spikes from starvation or cold, stabilizing their bioenergetic circuit.

Melanocyte Shift: The rising éR of the KT asteroid caused life forms who made it through the event to reject reptile and amphibian adaptation of chromatophores for the amplification of melanocytes. This was then tied to leptin-melanocortin pathways to make survival in a food-poor world possible for the early therapod dinosaurs and small mammals. This amplification and reliance of melanin due to altered light lowered éR by streamlining pigmentation energy costs. This shift supported UV protection and thermoregulation, key for endothermic stability, while avoiding the oxidative stress of older pigment systems.

Endothermy: As the most unappreciated metric, quantum-tuned endothermy allowed both clades to maintain a controlled éR baseline. By optimizing mitochondrial proton gradients and electron tunneling, they sustained metabolic work despite external chaos, counteracting entropy more effectively than ectotherms. Well done @MitoPsychoBio & @drmichaellevinImage
2. My discussion on the Tetragrammaton podcast with Andrew Huberman doves deep into the role of melanin in quantum processing, and my breakdown aligns with many of the concepts they explore while adding a quantum biological spin. Let me unpack how melanin amplifies quantum processing in mammals, mainly through electron surge, spin coherence, and energy bandwidth, and why this was a game-changer for Eutherian mammals and birds post-K-T event.

I’ll also tie this back to the Energy Resistance Principle (ERP) of Picard and Levin and then link it to the very unappreciated metric of quantum-tuned endothermy, while addressing the cellular impacts and evolutionary implications I’ve raised for 20 yearsImage
3. Melanin’s Role in Quantum Processing
As discussed in the podcast, melanin is a wide-bandgap semiconductor that absorbs light across a broad spectrum (all 73 octaves) far beyond chlorophyll’s narrow 400-700 nm range. This property allows melanin to harness light energy in ways that plants can’t, fundamentally altering how animals process energy and information at a quantum level. This would have been highly adaptive when the sun was blocked because of how chlorophyll operates with sunlight to create all the food webs. In evolution, chlorophyll came first, then hemoglobin, and then the KT event amplified melanin biology when the sun was dimmed.Image
4. Electron Surge
In the classical mitochondrial electron transport chain (ETC), electrons from food (via NADH and FADH₂) fuel a cascade that generates a proton gradient (ΔµH⁺) for ATP synthesis. As I've noted, this yields about 4-10 electrons per glucose molecule, a process well-documented in bioenergetics literature like Nicholls’ Bioenergetics (2013).

However, melanin introduces a quantum leap by splitting water (H₂O → 2H⁺ + ½O₂ + 2e⁻) under light exposure, a phenomenon I call “human photosynthesis.” This reaction, driven by UV and visible light (200-700 nm), generates a flood of electrons—potentially 10x more than chlorophyll’s output in plants.Image
5. This electron surge supercharges the ETC:

Complex I Overdrive: The influx of electrons from melanin-driven water splitting overwhelms Complex I, ramping up proton pumping into the mitochondrial matrix. If the matrix typically handles 10⁸ protons, this could scale significantly, densifying the proton gradient during the KT event.

Entanglement Scaling: The increased proton (H⁺) density enhances spin entanglement, a concept I have referenced with Binder’s work (2015). Protons, with their ½ spin, form a quantum network where entanglement scales as √N (where N is the number of particles). More electrons and protons mean a denser spin network, potentially accelerating quantum processing from linear to exponential rates.Image
6. Spin Coherence

Del Giudice’s coherent domains (CDs), as you mentioned, are regions in water where H⁺ spins align due to quantum electrodynamics (QED) effects, creating a “super-coherent” state.

In the podcast, I emphasized how melanin in the retinal pigment epithelium (RPE) and skin absorbs light, splitting water and generating H⁺ spins that align across these CDs.

Unlike the food-driven pathway, which relies on a slower electron trickle, melanin’s full-spectrum absorption (UV to IR) sharpens spin coherence. This move was all about taking full advantage of light when it became rare and scarce. This is what drives change. Why? Shannon 1948 paper: For a signal to have meaning, it must be rare or unusual.Image
7. How do we sharpen spin coherence?

Light Tuning: Visible light (532 nm, via the photomolecular effect) and UV (4 eV) excite melanin, aligning H⁺ spins more tightly. Del Giudice’s work (1988) suggests that such coherence extends NMR relaxation times (T₁), reducing decoherence.

Exclusion Zone (EZ) Synergy: Pollack’s EZ water, often static, shields CDs from environmental noise, but melanin adds dynamic spin-spin coupling (J-coupling), amplifying coherence across cellular scales.

Melanin’s semiconductor properties—its chaotic electron delocalization—mirror CDs, creating a quantum network that processes information faster and more robustly.Image
8. Energy Bandwidth

Mitochondria traditionally operate within a narrow energy bandwidth (250-780 nm), with cytochrome c oxidase absorbing 650-950 nm to drive proton pumping.

Melanin obliterates this limitation:

Broad-Spectrum Absorption: From IR (1 eV) to UV (6 eV), melanin captures energy across a continuous spectrum, eliminating the bandgap constraints of chlorophyll or even mitochondrial enzymes. This floods the ETC with electrons and biophotons (200-350 nm, as noted by van Wijk, 2014), which act as signaling molecules.

Quantum Processing Leap: The entangled H⁺ spins, now operating across a wider frequency range, enhance ATP synthesis (via F₀ torque in ATP synthase) and enrich redox signaling (e.g., ROS-driven pathways like NF-κB). This broader bandwidth allows cells to process energy and information simultaneously, a quantum advantage over food-only systems. you are now entering Uncle Jack's world where LIGHT is great than food and why Leptin Rx works.Image
9. Cellular Impact: The Quantum Leap for Mammals
Melanin’s amplification of quantum processing had profound cellular and evolutionary impacts, especially for mammals and birds post-K-T event:

Mitochondrial Battery: The increased H⁺ density from melanin’s water splitting packs the mitochondrial matrix, scaling entanglement density. If a typical cell manages trillions of quantum interactions, melanin could push this to quadrillions, as I've suggested. The piezoelectric effect on ATP synthase (F₀ torque) amplifies, generating higher voltages and faster charge cycles—light-driven, not food-lagged.Image
10. What else was optimized?

Coherent Domains: Melanin’s electron flood synchronizes water oscillations in CDs, tightening spin-spin coupling. Visible light (2-3 eV) splits water, while IR (1 eV) tunes CD oscillations, creating a multi-scale quantum processor from mitochondria to neurons.

Cell Signaling: Biophotons from melanin’s UV burst (200-350 nm) enhance signaling depth, following Fermat’s law as refractive indices shift in cellular media. Spin-driven redox pathways (e.g., NF-κB) and circadian clocks (via cryptochromes, CRY) synchronize, turning energy into information with unprecedented speed and reach.

Life was introduced to the dissipative state where it was 4 standard deviations over where reptile were before who kept melanin just on their interiors. Mammals put it everywhere.Image
11. Why Melanin Changed Everything

Chlorophyll locks plants into a visible-spectrum niche, relying on mitochondria to process leftovers. As I have highlighted for 20 years now, melanin lets animals harness all light that comes to Earth 24/7, turning H₂O into an electron and proton geyser. This explosion of cells' quantum capacity enabled mammals and birds to survive the K-T event.

Post-K-T Advantage: With sunlight dimmed by impact dust, melanin allowed these clades to generate their light (biophotons) and energy, decoupling them from photosynthesis-dependent food chains. Their mitochondrial capacity, amplified by melanin, sustained endothermy and flight (birds) or metabolic flexibility (mammals).

Quantum-Tuned Endothermy: Tying this to the ERP, melanin lowered éR by optimizing energy transformation. The electron surge reduced dissipative losses, while spin coherence minimized oxidative stress, allowing these animals to maintain metabolic stability in chaos.

Cultural Context: My reference to “Anubians at 28°N” suggests ancient humans in sun-rich regions (e.g., Egypt) maximized melanin’s potential, their mitochondria “singing” with quantum efficiency. Modern humans, in “LED caves,” just like the elite of Egypt buried in the gold sarcophagus disrupt this with blue light, stalling quantum processing and elevating éR—leading to disease, as the ERP predicts.Image
12. Melanin as Life’s Regenerative Current
My nod to Robert O. Becker’s regenerative current aligns with Kruse’s emphasis on light as life’s driver. Melanin’s ability to “hydrate melanin to dampen the ampere” (modulate electron flow) mirrors Becker’s DC currents in regeneration. Del Giudice’s QED framework supports this: melanin’s electromagnetic chaos entangles CDs, outstripping Pollack’s static EZ water or Chaplin’s non-spin clusters.

Life, as I say, is a “quantum dance of light,” and melanin orchestrates it, bringing mammals back from the brink of extinction.Image
13. LESSON OVER Image
Image
14. Extra credit: Why is grass that undergoes slow decay always greener? Because anything green reflects green light and absorbs tons of blue and red and becomes more energy efficient because éR in the ETC of the grass is channeled to useful work and not lost by the plant. This insight is why I came to rationale to patients in January 2020 at the beginning of COVID to use MB to combat DARPA's COVID.

MB is blue and as such anyplace it flows will rejec the absorbtion of blue light. This means mtDNA would absorb more UV because MB increases NAD+ to do just that at 340 nm. It also would force more red light absorbtion at the Q cycle and cytochrome C oxidase to help the ATPase spin and the Q cycle deliever electrons to cytochrome C oxidase to keep cardiolipin damage at bay. The reason I knew hospitals would kill millions is because with COVID hypoxia they would default to oxygen therapy which would make the electrical resistance drops in ECT when oxygen is added due to its electronegativity. None of my ICU collegues listened to me but as soon as I started pushing MB when they left shift their patients got better. Vitamin C will do the same but MB is way better at the process.

MB and Mitochondrial Resistance: MB, by oxidizing NADH to NAD+,this influences the ETC (step 7). By increasing NAD+ availability, MB reduces the "load" on Complex I, effectively lowering resistance to electron flow and boosting ETC efficiency. This helps maintain the proton gradient (ΔμH⁺, step 8) and ATP production (step 9), counteracting mitochondrial dysfunction.

Melanin and Tissue Resistance: Melanin, a dark semiconductive pigment, contributes to tissue-level resistance by facilitating electron transfer in response to light. If melanin is dehydrated or absent, tissue resistance might drop (oxygen problem = ARDS), disrupting energy flow. MB compensates for these effects by acting as an alternative electron carrier, effectively increasing resistance in a controlled way to restore proper energy transformation.

Deuterium and Resistance: I've also mentioned for 20 yrs that deuterium’s impact on the NADH/NAD+ couple, which slows ETC speeds and disrupts the Q-cycle. Deuterium increases resistance in a detrimental way by slowing electron transfer (step 7). MB, by promoting NAD+ production with H⁺ (not deuterium), reduces this aberrant resistance, restoring efficient energy flow. MB can affect the spin effect of the extra neutron in deuterium. This is why it works in cancer too.

Neurosurgeons who do a ton of trauma cases know MB it modulates éR in the ETC to ensure energy is directed into useful work (ATP synthesis) rather than being lost as heat or ROS. If you remember the podcast with @JonesDanny and I talked about the one neurosurgery case that changed my life, the little girl I operated on all night during @Metallica 24 playlist, I had MB running in most of the night as I worked to remove the bone from her brain.

I was worried about this 16 yr old being able to recover from these injuries so I went peddle to the metal on MB. Way outside the package insert. Why?

MB use has broader implications: Resistance in Distributed Biological Systems

I knew that her neural, vascular, and other anatomical networks distribute and transform energy into information by varying resistance regions (éR) across massively distributed membrane systems working in parallel alignment. My profound insight that night almost got me fired when I told my staff doctor to get the fuck out of the room. Why did I go all in?

Neural Networks: The brain’s parallel processing relies on varying resistance across billions of neurons and synapses. This allows energy (ion gradients, bioelectricity) to be transformed into information (thought, memory, behavior). I wanted to perserve as much of her cognition as I could as I worked. This was the same idea I had on Rick Rubin for his open hear t surgery. Peter Attia told Rick I was nuts but Rick has that little girl to thank for the advice I gave his Stanford surgeon. The surgeon did not take it, but Rick did. He trusted me. Now the Famous Attia knows something he did not before. Not surprising since he never finished a residency so his clinical skills are not what they could be.

Vascular Networks: The circulatory system uses resistance to compute how to distribute energy (oxygen, nutrients). For example, during hypoxia (as in COVID-19), resistance in pulmonary vessels increases to redirect blood to better-oxygenated lung regions (a process called hypoxic pulmonary vasoconstriction).

Cellular Networks: Mitochondria within cells form networks that dynamically adjust resistance based on energy demand. For instance, during high ATP demand, resistance in the ETC decreases to speed up electron flow, while during low demand, resistance increases to prevent ROS production. Preserving Ricks cochlea from ROS damage was key in my recs to him on bypass.

In all these systems, resistance isn’t static—it’s a dynamic variable (éR) that organisms adjust to direct energy flow and process information. This mirrors how microcircuits use resistors to control current and perform computations. Seems like MB effects are well known by mitochodnriacs. I wonder why? ;)Image
@threadreaderapp make me a roll

• • •

Missing some Tweet in this thread? You can try to force a refresh
 

Keep Current with ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆

☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 Profile picture

Stay in touch and get notified when new unrolls are available from this author!

Read all threads

This Thread may be Removed Anytime!

PDF

Twitter may remove this content at anytime! Save it as PDF for later use!

Try unrolling a thread yourself!

how to unroll video
  1. Follow @ThreadReaderApp to mention us!

  2. From a Twitter thread mention us with a keyword "unroll"
@threadreaderapp unroll

Practice here first or read more on our help page!

More from @DrJackKruse

Feb 10
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.

CITE

optimalklubs.com/kruse-for-dumm…Image
Image
Image
Image
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.
Read 24 tweets
Feb 5
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.
Read 38 tweets
Jan 31
Here is the irony: Attia advice was wrong.

**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.
Read 5 tweets
Jan 31
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.Image
2. Integration with Melanin and the Sun

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.Image
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).

patreon.com/DrJackKruse
Read 7 tweets
Jan 29
Plan B in El Salvador is all about the Tether gold play. This is how they want to rescue things for the surveillance state. Image
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.Image
Read 5 tweets
Jan 29
1. New lesson today from my forum for the Savages to consider. This tweet below is the primer.
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.

x.com/drjackkruse/st…

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
HsCRPImage
Image
Image
Image
3. Back round info on U/S: westonaprice.org/health-topics/…
Read 15 tweets

Did Thread Reader help you today?

Support us! We are indie developers!


This site is made by just two indie developers on a laptop doing marketing, support and development! Read more about the story.

Become a Premium Member ($3/month or $30/year) and get exclusive features!

Become Premium

Don't want to be a Premium member but still want to support us?

Make a small donation by buying us coffee ($5) or help with server cost ($10)

Donate via Paypal

Or Donate anonymously using crypto!

Ethereum

0xfe58350B80634f60Fa6Dc149a72b4DFbc17D341E copy

Bitcoin

3ATGMxNzCUFzxpMCHL5sWSt4DVtS8UqXpi copy

Thank you for your support!

Follow Us!

:(