Remember the battle for the Nobel Prize between the discovery of HIV from Montagnier versus Robert Gallo in 1983?
Do you know that Robert Gallo began studying HIV in the jungles of the Congo in chimpanzees during the oral polio virus trials.
The first oral polio vaccine was aerosolized oral spray that caused cancers all over the mouth and sinus system. A bioweapons company did the work for DoD and Robert Gallo was on that team. Things you just do not know when you do not know your history. Did you know that Fauci support the Nobel Prize for his friend Gallo over Luke Montagnier?
Coincidence or might it be related to why Reagan hired Fauci in 1982?
3. The first bioweapons lab on Magazine Street in NOLA and the work done at the US Public health hospital and Henry Clay Street in NOLA was transferred to the Tulane Primate Center in Covington Louisiana under the direction of Dr. Riopelle. When it became clear after the JFK killing in the mid 1960s that these simian viruses were behind many new human diseases like cancer and eventually HIV they were transferred to Fort Detrich as I laid out in my pod with RFK Jr. In the beginning Fort Detrich was an dual purpose base with the ARMY and CIA sharing thefacility and the bioweapons labs added to the mix as the science of Dr. Mary Stewart and Mary Sherman was developed by the CIA and industrial military complex.
4. The bioweapons lab in NOLA gave the military important bioweapon clues. Namely that nnEMF drive pathogenicity and it could be concentrated if many different viruses from competeing species were mixed before irridation. They were very deadly. These things were developed at Fort Detrich from 1963-68 in experiments called the Special virus leukemia Program.
5. This shows you where the military was in 1968. They were at a macro level dealing with data points in dead animals looking to see what was most effective in killing them. The miliatry was not the molecular level that one would need at furin cleavage sites to know the proper AMO physics to carry our mass death in living things. That science developed after Reagan hired Fauci in 1982.
When one plots the data of chronic diseases to when Fauci entered the industrial military health complex the data points do not lie. They tell a story that shows you it it not a story about food. It is a story of AMO physics and light to ruin mtDNA biology.
6. The most interesting finding from this Fort Detrich program was that the industrial military program was not looking to cure cancer, it was looking to make it more lethal. They found using animals closest to the human genome were the most deadly to humans. And then they amplified the effect through the early Nixon administration. @Kevin_McKernan The pathway to policy was clear. A new bioweapon policy was developed around vaccines using gene products needed to be developed by the military. This is where the ideas were born.
7. This paper really shows the origin of HIV. When the industrial military complex decided to mix the serum or primates and human serum togther and monitor the effects some very interesting findings started to show up in the literature early in Nixon's administration. This was 2 years before Nixon and Alton Ochsner launched the "War on Cancer" policy. That policy was designed to create a pile of money for covert bioweapon development. This money was laundered from the NCI to the military to continue on the pathway that General Groves began with Ochsner in NOLA during the Cutter Incident.
8. In 1970 they moved into the molecular medicine to see where the cancers can be recombined with across species. These are the genesis of gain of function studies done on US soil. This was legal before the 2001 Patriot Act. Now it is illegal and carries the penalty of death by Treason.
9. The last tweet shows you how viral chimera's were first built. You need to know that scientific accountability under our Constitution has not changed much since WW2. It rests with the Executive branch and this is why Gen. Groves capture this branch first in his silent coup on America by his shadow government. Why is this slide important. You'll notice the myriad of boxes who have to perform oversight for science and scientific misdeeds.
Groves had a lot to do with setting this system up because it gave the government scientific denialble plausibility in cases of misdeeds. I explained this to @nayibbukele when we met about the Constittional Amendment for his country. I told him RFK Jrs plan would not stop the problem with a Benjamin Rush like Amendment added to the ddcument because the industrial military complex knew this was the DOCUMENT's main weakness and they could exploit it using chronic disease management.
10. The next slide should give you chills. In 1969 they told Congress exactly what they were up to in viral chimera building and why they were doing it. Congress had ZERO issues with it and they allowed this via the oversight process. This was FUNDAMENTALLY why I disagreed with Bobby during the Tetragrammaton podcast with Rick on how to handle the chronic disease epidemic at its source.
We need a Constitutional Amendment to stop this freight train of the Deep State actors. This is when the military began to ensnare and capture the legistaltive branch of government. @KONCRETE
11. The industrial miliatry complex knew exactly what they were doing and Congress and Nixon helped them. If you listened to what I said about Nixon and what Bobby said about Nixon you'll notice we differed on our opinions of his legacy. This Act to Congress explicitly said that the military was now capable of making a bioweapon that would be immune to human immunity.
12. For the non believers that your own government did this, this is the entire logic chart they used in the annual report of the project from 1972 when the War on Cancer was used as a psy-ops on America.
13. Fort Detrich was where mammalian viral pathogens were mixed in lab test tubes accross multiple species like cards in a casino deck to try to find the nastiest disease the miliatry could use to kill effectively. The slide below shows you the basic of how the system was developed by your own government.
14. So when someone asks you where disease really begin........and you answer food. You're an idiot because you have no idea about the history of how this process began with the Manhattan Project in the 1930s.
15. Once they created a virus that could collapse the enture immune system, they decided to find out how to alter immunity so that diseases could come on faster. Here was a paper I was assigned to read as a neurosurgery resident to understand the biology of the fast growing cancer called GBM in humans. Most autoimmune conditions are related to these mechanisms. Many cancers are. Many other chronic disease epidemic diseases are also linked to neuroimmune defects.
16. Why was Peter Duesberg an HIV denier. If you read the literature as I did, you'd know why. He knew where it came from. This is the same story we just saw with COVID that happened 40 years ago in HIV.
17. Deusberg knew what many of us knew that simian virus was grafted onto the human system and the vector was the VISNA platform. The result was the HIV "1983 discovery" It was no discovery at all. Any financial forensic journalist could perform a details accounting to find out where the money came from and went to, to figure out this "medical enigma"
18. This is the patent to making the monster Hepatitis B vaccine that all physicians had to take. Note the highlighted area. You now see 20 yrs after the list of simian viruses the military was using they were now producing vaccines with the science as a delivery mechanism. Now you can see why there was a need for Fauci 7 years later and the vaccine law in 1986 when the techniques moved from the DoD to BigHarma partners.
19. That Hepatitis patent was used by Merck in their Heptavax trial in 1978. That trial was the basis of why every healthcare professional and soldier had to take this jab. So I know my history and I know what the government is capable of. It is time some of you get your heads out of your ass and know it as well.
20. What was in the COVID jabs? Simian virus 40 promotor.
21. @threadreaderapp make me a roll
• • •
Missing some Tweet in this thread? You can try to
force a refresh
1. QUESTION ON MY FORUM: Hello to everybody. I am 56 and into permaculture, I learned about decentralised medicine from Dr. Jack Kruse about 1.5 years ago since than I am following him and created an account on the forum a few month back I also subscribed to the Patreon blog and I am considering myself a noob and I have sill so much to learn. I am applying the things as I am learning in my own life and among my family members as they are willing to listen and to learn. My mother had a brain tumour decades ago which led to the removal of her hypophisis and a long list of medications and side effects in all the years. We are living in Spain at the Costa del Sol / Andalucia close to Malaga. I would describe it as slow, steady transformation of our lives. I am thankful to Dr. Jack Kruse and all the people involved in the decentralised medicine movement empowering the people.
But this post is not about myself, my friends son 26-year-old was diagnosed after multiple seizures in the middle of May.
I'm looking for thoughts from anyone with experience of low-grade gliomas, particularly in the insular/temporal region.
So far:
MRI suggests an infiltrating left temporo-insular glioma.
Initially measured 45 × 55 × 40 mm ( mid May)
Latest MRI measures approximately 50 × 55 × 55 mm (about 6 weeks later)
The tumour does not enhance with contrast.
Functional MRI and tractography show it lies very close to the language network (Broca's, Wernicke's and the left arcuate fasciculus).
He has no neurological deficits apart from the seizures, which are now controlled with levetiracetam.
The neurosurgical team is considering awake surgery and has completed language mapping in both English and Spanish.
They are still waiting for surgery (scheduled for September, no exact date yet), so they do not yet have a biopsy or molecular diagnosis.
2. ANSWER: If the kid does not learn how to "magentically pin" his proteons and electrons = singlet oxygen = glioma.
3. DISCUSSION: My work connects Otto Warburg’s vintage bioenergetic principles to modern quantum mechanics and the dark history of institutional science.
By detailing how a drop in cellular voltage opens the door to functional hypoxia, matrix deuteration, and the collapse of the mitochondrial F₀F₁-spin motor, I have laid bare the exact biophysical mechanism behind cancer and metabolic disease.
The 1910 Flexner Report was the tool used to deliberately steer Western medicine away from cellular biophysics and electrophysiology. It was a biological Landauer attack.
By standardizing medical education around a petrochemical-pharmaceutical model, it reduced the complex, spin-polarized human matrix into a simple chemistry set to be treated with synthetic, patentable pills.
Here is the strict decentralized first-principles breakdown of the structural model that Warburg started, and that modern quantum biology completes.
Ketogeneic diet provides more H+ and less D+. For GBM this is a benefit but DDW use works way better. Why? Because water provides the matrix more H+ to offset the UCP-2 deuterated gate.
Isotopic fractionation is only part of the story of cancers like GBM. I know I have treated hundreds of them over 40 years.
What has centralized science missed? THE KEY PART.
For the first 2 billion years of life, the Earth's magnetic dipole field was weak, fluctuating, and unorganized. Because the planetary magnetic field lacked the strength to stabilize spin states across large scales:
High Quantum Friction: Lacking a strong magnetic field to stabilize spin orientation, early anaerobic organisms could not efficiently utilize Chirality-Induced Spin Selectivity (CISS). Electrons scattered wildly, generating massive amount of thermodynamic waste heat and raw free radicals. Without a dynamo, oxygen stays in the singlet state. It never gets into the triplet state. In complex tissues like the BRAIN, this is the key to cancer in the brain.
Chemical Constraints: Without organized spin-pinning, life was forced to operate at a slow, low-energy metabolic pace. The human brain cannot tolerate this. As a result of a weak dynamo, the brain gets stuck in the "biochemical mud" of singlet state oxygen (Warburg shifted) relying on primitive fermentation, local chemical gradients, and simple, flat molecular structures. Complexity was strictly capped by the high thermodynamic cost of electron scattering due to inability to polarize electron spin to build coherence.
The Neoproterozoic "Stall": During the weak-field era prior to the Cambrian, there was no "Magnetic Pin" to distinguish between mirror-image molecules. This is why there was no complex brain evolution as yet. Electron spin was chaotic and could not be organized to the triplet state. Life stayed in a low-energy, Singlet-trapped state because it couldn't "rectify" the signal. Nick Lane, Seyfired, and you still do not realize this basic fact, but I have for 25 years. DIET CANNOT FIX A GBM.
2. Why are all GLIOMAS linked to low Vitamin D status. No centralized MD or PhD has a clue why this happens.
I teach decentralized Medicine to these people PRECISELY why it happens.
3. WHY IS LOW VITAMIN D ALWAYS ASSOCIATED WITH GBM? Without the sun you have no melanin in which to drive CISS quantum biology to feed H+ and triplet state oxygen into your brain's mito matrix. This leads to the cancer.
What don't functional allopathic clinicians see that decentralized ones do? They do not understand the spin state of the photon and how chirality fits in this story. Why taking Vitamin D supplementation does not equal skin in the game. You didn’t just pop a vitamin D pill. You tried to hijack a cosmic symphony, a blazing, stellar-forged photonic command chain that ignites when UVB photons, spun with the raw angular momentum of a whirling star, slam into your skin’s crystalline water grid.
This isn’t a nutrient; it’s a celestial spark, a quantum handshake between a star and your cells, locked in perfect frequency, angle, and orbital rhythm. These photons don’t deliver a substance; they unleash energy and code. They surge through your dermal layers, flipping magnetic fields, ripping open voltage pathways, and rewiring redox gradients. Your mitochondria?
They’re not just powerhouses; they’re torsion-driven quantum processors that order the spin of electrons from food before they enter the ECT.
Electrons have to be humming with the PROPER SPIN to the beat of Faraday’s Law:∮ E·dl = −dΦᵦ/dt. This is a law no one in centralized biology ever learns.
A shifting magnetic flux drives electric currents through a closed loop, and your body is that loop: BRAIN, skin, water, charge, geometry. When the photon hits, cholesterol twists, membranes polarize, electron clouds morph into structured torrents. Enzymes like CYP2R1 and CYP27B1 don’t sense molecules; they feel tension.
The VDR doesn’t care about presence; it craves resonance and that resonance require electron spin to be parallel.
Only when your nuclear matrix syncs with the incoming solar wavefront does the genome throw open its gates, transcribing over 900 genes in lockstep with this stellar pulse carrying spin data.
But that capsule you swallowed? It’s a hollow echo, a molecule stripped of its cosmic fire and the spins are chaotic. No flux, no curvature, no induction, just a shadow without a sun. Your chemistry churns, but the quantum corridor stays dark. The waveform never crashes.
The chromatin twists, but it’s out of tune, like a satellite drifting without its planet, not broken but grieving. The star’s signal burns on, but your receptors are out of phase. Their circadian phase is not locked, and your genome and immune system become unprotected. The contract was electromagnetic, and coherence doesn’t negotiate. Break the symmetry, as Noether warned, and something, some spark of cosmic alignment, is lost forever. Step into the light, or stay in the shadow. The universe doesn’t wait for anyone to get things right. The lesson is all in the slide. No functional, allopathic, or centralzied MD knows this and this is why they keep ordering labs on you, telling you a ketogenic diet is a panacea when it is not in GBM.
Overcoming the Environment: Sun, Blue Light, and "Grounding" Your lifestyle profile tells the story. You avoiding the sun, being very pale, living in a city environment dominated by artificial blue light, and lacking contact with the earth, adds major environmental friction to an already compromised immune system.
The Sunlight & Acid Connection: Avoiding the sun causes deep Vitamin D receptor starvation. Vitamin D is a primary epigenetic regulator of T-regulatory (Treg) cells, the "brakes" of the immune system. When Vitamin D is chronically low, Treg cells fail, allowing the auto-reactive CD4+ T-cells to aggressively attack your stomach lining unchecked. Furthermore, sunlight exposure triggers local proopiomelanocortin (POMC) cleavage, which aids in autonomic nervous system balance, is essential for the vagus nerve to stimulate stomach acid production.
The Blue Light & Circadian Inversion: Living in an artificial blue-light environment under the constant glare of screens destroys your evening melatonin production. Melatonin is a potent mitochondrial antioxidant. The stomach lining has a incredibly high density of melatonin receptors because it relies on overnight sleep cycles to repair the mucosal lining from daytime acid exposure. High blue light at night prevents this repair cycle, leaving an already inflamed stomach vulnerable to faster atrophy.
The "Grounding" and Tech Physics: From a biophysical perspective, constant exposure to electromagnetic frequencies (EMFs) from city technology without physical contact with the earth alters cellular voltage-gated calcium channels (VGCCs). When VGCCs are chronically excited by ambient fields, it drives intracellular oxidative stress, fueling the fires of systemic inflammation.
I hope your audience learns a lesson. Do not listen to your advice. You're diagnosis puts you closer to death than longevity and it is entirely tied to your choices and beliefs.
2. How would the MITF-AMPAR pathway feed into this situatioon since you've slef blocked the sun to get this autoimmune condistion?
If we theoretically block the sun (removing ultraviolet radiation/UVR), the impact on the MITF-AMPAR pathway interacts with the risks of autoimmune gastritis (AAG) through two primary mechanisms: systemic autoimmune cross-reactivity and altered oncogenic potential.
In the context of cellular signaling, AMPAR (ionotropic AMPA glutamate receptors) and MITF (microphthalmia-associated transcription factor) form a crucial regulatory loop. Normally, keratinocytes release glutamate, activating AMPAR on neural-crest-derived cells. This activation upregulates MITF to manage cellular survival, differentiation, and structural integrity.Simulating a scenario without sunlight alters this biological feedback loop and influences the risk profile of gastritis in several distinct ways:
1. Accelerated Melanocyte Detachment and Vitiligo Co-occurrence
The Pathway Breakdown: Sunlight (UVR) typically triggers the systemic production of alpha-MSH, stimulating MITF expression. Concurrently, glutamate signaling via AMPAR sustains MITF to preserve the physical structure and adherence of melanocytes. Blocking the sun downregulates this pathway, leading to a loss of cellular actin microfilaments and causing cells to "round up" and detach.
The Gastritis Connection: Landmark comparative pathologies published on Authorea show that Vitiligo (melanocyte destruction) and Autoimmune Gastritis (parietal cell destruction) share an identical initiating mechanism: cellular detachment driven by adhesion loss.
In a sunless environment, a collapsed MITF-AMPAR loop triggers widespread melanocyte instability. This cellular debris presents highly concentrated target antigens to CD4+ and CD8+ T-cells, priming systemic auto-reactivity. This heightened immune state can cross-activate T-cells against the gastric mucosa, driving or worsening AAG.
3. Phenotype Switching and Aggressive Gastric Cancer Progression
The Pathway Breakdown: MITF functions as a cellular "rheostat". High MITF expression promotes normal differentiation and localized proliferation. Low MITF expression drives a "phenotype switch," shifting cells into a highly invasive, migratory, and stem-like state.
The Gastritis Connection: As detailed in the earlier discussion on AAG risks, chronic gastritis frequently progresses down the Correa cascade into Gastric Cancer (GC). If the sun is blocked, the withdrawal of UV-induced signaling combined with an inactivated AMPAR loop sharply downregulates MITF. In patients where gastritis has already triggered early-stage neoplastic cells, this low-MITF state acts as a genetic green light for metastasis. It accelerates the transition from standard metaplasia to aggressive, invasive gastric adenocarcinoma.
I told @mattkratter that I thought BIP-110 did not go far enough. I think the real sin by Core was Segwit. But the Fabian plan is always to use small changes so no sees the real attack. It's activation was highly sketchy and smells of Fabiansm thought at MIT where the math & physics guys thought of this in Thiel's secret meetings with Epstein. If we added an inversion to Segwit discount, meaning make it cheaper to put non monetary gains data in Op Returns it would make the attacker have to bear a steep opportunity cost to pollute the UTXO set. I was told that Luke thought as I did that BIP-110 needs more bite. @LukeDashjr On that you'd have to speak with him on his opinion. He and I are in different spheres.
2. SegWit (Segregated Witness) was primarily developed and conceptualized by lead Bitcoin Core developers Pieter Wuille, Eric Lombrozo, and Johnson Lau. Wuille first presented the scaling upgrade at a Hong Kong conference in 2015, and it was subsequently integrated into the main protocol in August 2017. If you follow the trial it leads right to Runes/Ordinals. This is how I was clued into the play. This leads right to C-SAM and back to MIT and Epstein. Chaincode Labs is Wuille's baby.
3. The reason why people, including prominent developers, associated with the SegWit activation call it "unusual," "highly sketchy," or deeply controversial boils down to the fact that it was activated via a high-stakes political standoff, corporate backdoor agreements (MIT math and physics guys heavily involved), and an unprecedented game of economic chicken that nearly split the Bitcoin network in two.
Within Bitcoin’s technical community, the math behind SegWit was widely accepted. However, the actual activation process in 2017 bypasses normal software rollout consensus and is considered "sketchy" for several key reasons.
Harry Nyquist strikes at the absolute heart of quantum biology. By drawing a line from the telegraph smearing of the 1920s to the 30-million-volt inner mitochondrial membrane (IMM) capacitor, I have identified the ultimate bottleneck of life: the IMM is a finite communication channel, and it has a strict, mathematically defined bandwidth limit.
In standard medicine and biochemistry, the solution to metabolic failure is always "brute force", push more substrate, take more supplements, inject more insulin, or increase the caloric throughput.
This is the exact equivalent of the 1920s telegraph operators trying to send messages faster by pumping stronger electrical currents through a low-bandwidth copper wire.
As Nyquist proved, brute force does not create clarity; it creates distortion (aliasing). In the mitochondrion, that distortion manifests as NADD+ and singlet oxygen. Big time lesson here why most influencers are retards.
2. Nyquist is also famous for discovering Johnson-Nyquist noise, the unavoidable thermal agitation of electrons inside an electrical conductor, which occurs regardless of the quality of the hardware.When the IMM's bandwidth is exceeded, the system can no longer handle the information digitally or coherently (as ultra-weak biophotons).
Because reality has bandwidth and energy cannot be destroyed, the blocked electronic information drops directly into the thermal domain. The organized quantum potential of the 30MV/m field degenerates into thermal agitation = heat entropy that is the Landauer liquidation of disease.
This localized explosion of thermal noise is the exact biophysical engine of the mitochondrial "hot flash", it is the cell dumping its unprocessable, aliased data stream as non-coherent infrared waste heat.
3. Rockefeller biochemistry operates on the premise that if a machine is failing, you must throw more fuel, more chemical force, or more corporate pharmaceuticals into the wire. Nyquist teaches us the exact opposite. If the channel is limited, brute force only creates more distortion. To fix a diabetic beta-cell or a mutating cancer cell, you do not "send more." You must shape the signal and restore the medium.
You shape the signal by removing the non-native harmonic distortion of nnEMF and polarized blue screens or a lack of magnetic pinning.
You restore the medium by using grounding and native infrared light to rebuild the liquid-crystalline water table, re-pin the magnetic flux, and pull the IMM back up to its pristine 30 MV/m operating capacity.
Only when the channel's structure is respected can the ATPase nanomotor spin frictionlessly again, processing intelligence without dropping it into thermodynamic ruin.
It should be obvious now that deuteration of the water table due to a loss of the 30 million volt charge on the IMM alters the 9,000 RPM spin rate of the ATPase in tissues with mitochondria, and this is where time entropy comes from in disease.
If we view this through the lens of Nikolai Kozyrev’s Causal Mechanics, these physical jams represent a rapid drop in local time-density, forcing the tissue to generate time-entropy (disorder) and lose its topological quantum protection.
Kozyrev established that any process that increases entropy or causes chaotic scattering actively releases time, reducing local time-density. Within a mitochondrion, the presence of D+ creates a severe, localized thermodynamic breakdown:
The Mechanical Stutter: The F1 F0ATP synthase nanomotor is a nanoscale centrifuge designed to spin at speeds up to 9,000 RPM, driven exclusively by the single-proton (H+) motive force. When a heavy deuteron (D+) slips into the channel, its doubled mass and vastly different quantum tunneling profile cause a physical mechanical stutter.
The Breakdown of the Stator: Kozyrev proved that rotating, asymmetric systems interact directly with the density of time. The ATP synthase is a literal biological stator. When its fluid rotation is jerked and disrupted by a heavy isotope, its uniform angular momentum collapses into micro-vibrational chaos.
The Entropy Shift: Because the motor stalls but the metabolic pressure from the Krebs cycle keeps pushing, the electrochemical energy cannot be cleanly converted into ATP. The orderly, low-entropy vector flow (Delta S to 0) fractures. Energy arcs across the membrane, radiating outward as uncoupled heat and Ultra-Weak Photon Emission (UPE). This uncontrolled dissipation is the physical manifestation of time-entropy which is seen as a rising heteroplasmy due to disordering of IMJ geometry through a microscope. Picard et al found this in his work.
2. The Chrono-Thermal Matrix: Temperature as the Quantum Vice
Integrating my Cold Thermogenesis (CT) protocol and ELOVL-ELongation framework completing the loop of biological time-entropy control. In my model, temperature is the primary physical dial that regulates the fluid dynamics, isotopic purity, and temporal coherence of the mammalian lipid architecture.
When environmental temperatures drop, the cell applies a localized "Quantum Vice" to the enzymatic assembly lines on Chromosomes 2 and 6, forcing an absolute thermodynamic selection for Light Hydrogen over Deuterium.
3. The ELOVL/FADS Architecture: Epigenetic Isotope Filtration
The synthesis of highly fluid polyunsaturated fatty acids (PUFAs) like Docosahexaenoic Acid (DHA, 22:6n-3) requires a coordinated dance between Fatty Acid Desaturases (FADS, which snip hydrogen to create double bonds) and Elongases (ELOVL, which add two-carbon units and four hydrogens to lengthen the tail).