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.
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The Malate-Aspartate shuttle and its role in connecting cytoplasmic and mitochondrial NAD+/NADH pools are linked to sunrise effects on TCA cycle stoichiometry. This connection arises because circadian cues from sunlight can modulate TCA cycle intermediates (like malate), which the shuttle relies on to maintain NAD+/NADH balance across cellular compartments. NAD+ has a 258 nm absorption spectra and NADH is 340nm. LIGHT is a huge part missing in this story.
2. Ionized Hydrogen (H+) in Mitochondria
Proton Jump Conduction (Grotthuss Mechanism): Within mitochondria, H+ ions (protons) are abundant in the matrix. These protons can move rapidly through water via the Grotthuss mechanism, which involves quantum tunneling. This mechanism allows protons to hop through the hydrogen bonding network, effectively creating superconducting proton cables that facilitate rapid communication.
Ionic Plasma Formation: When hydrogen is ionized, it forms an ionic plasma that behaves like a liquid metal. This plasma, enhanced by iodine, enables efficient charge transport within mitochondria and other cellular fluids like cerebrospinal fluid (CSF). The presence of iodine in CSF, for instance, helps form these superconducting proton cables, linking mitochondrial function to environmental signals.
3. Light Excitation of Electrons:
Mitochondria release infrared light, which interacts with the surrounding water to charge separate it into H+ and OH⁻ ions. This light also excites electrons within the electron transport chain (ETC), influencing the redox state and energy transfer efficiency. The interaction of light with water and mitochondria is crucial for sensing environmental changes.
Magnetic and Electric Fields:
Mitochondria, due to their high density of H+ ions and the presence of transition metals in the ETC, generate strong electric and magnetic fields. These fields can interact with environmental electromagnetic forces, such as those from the ionosphere or solar radiation, to modulate mitochondrial function. The paramagnetic nature of oxygen further enhances this interaction, drawing it towards mitochondria.
DNA's use of helical geometery seems to have a lot on common with the Cosmosi use of electric and mangetic flux in a Birkeland current's organization.
I'm drawing an intriguing parallel between DNA’s supercoiled, torsion-driven structure and the organization of a Birkeland current. Birkeland currents, observed in plasma physics (e.g., in space plasmas or auroras), are helical, twisted flows of charged particles guided by magnetic fields, carrying electric currents along twisted magnetic flux tubes. The sun does the same.
This similarity in helical geometry and energy storage is a fractal I have explored in many blogs. this is why polarization is a big deal. It is why sunglasses are a problem and this showed up in Becker's experiments on sleep.
The Sun and mitochondrial colony is connected in this way wirelessly.
Both systems rely on twist as a stabilizing and functional feature. DNA’s supercoiling stores mechanical torque (10-20 pN·nm) to regulate access and compact genetic material, while Birkeland currents use magnetic torsion to channel plasma and sustain current flow over vast distances.
In DNA, enzymes manage this torsion to control gene expression, akin to how magnetic fields guide and modulate the current in Birkeland structures. The idea of tension gradients in DNA mirrors the dynamic equilibrium of magnetic tension in Birkeland currents, where twist maintains coherence against chaotic dispersion.
Additionally, the role of structured water in DNA stabilization could parallel the plasma environment in Birkeland currents, where charged particles and fields interact to maintain structure.
Both systems suggest a self-organizing principle: DNA’s coil as a biological “engine” and Birkeland currents as a cosmic one, both leveraging geometry and torsion for energy management. While direct evidence linking the two is speculative, the shared physics of helical organization and torque-driven stability offers a fascinating conceptual overlap to explain how life connects to the fabric of the cosmos.
2. Everything in cells have a torsion. It is part of the AMO design inside of a cell which is another key to the mystery of the recipe of Nature. Torsion is the key regulator of energy tunneling: correct twist narrows the energy barrier, boosting tunnelling probability, while loose or damaged coils disrupt conduction. This is quantum control mediated by mechanical tension, measurable in experimental setups.
3. DNA’s selectivity is discriminating by wavelength, polarization, and direction which means it absorbs specific fields. When the right frequency hits, charge conduction increases, water layers shift, and genes unlock, pointing to field-gated biology.
This is why I have a problem with guys like Micheal Levin who say EMF is not a story in biology. This is pur bullshit.
Low-frequency EMFs can unwind or block access, while infrared from mitochondria restores torsional symmetry. Natural rhythms (Schumann, solar, circadian) serve as environmental tuning forks, influencing expression.
Chromatin loops and field-sensitive telomeres organize exposure, and gene expression becomes resonance matching, not just transcription.
Resonant coils store energy, transmit information, and respond to field alignment, mirroring DNA, which stores mechanical stress, converts torsion into access, and tunes to environmental signals. When aligned, this field-aware coil enables life to “speak fluently,” blending quantum biology with measurable physics at the edge of science.
2. Circadian biology uses what three metrics to control it, Jack? Light, dark, and temperature.
Potential Problems of living with Air conditioning?
Here’s a comprehensive list of potential issues, grounded in circadian biology and general health impacts:
Circadian Rhythm Disruption
Mechanism: Circadian biology relies on temperature as a zeitgeber (time cue). The body expects a gradual drop in core body temperature at night to promote sleep onset and maintenance. AC can create an unnaturally cold environment, potentially desynchronizing this process.
Effects: Difficulty falling asleep or staying asleep.
Reduced sleep quality (less restorative deep and REM sleep).
Altered melatonin production, as temperature dysregulation, can interfere with the pineal gland’s response to darkness.
Severity: Moderate, especially with chronic exposure, as it can lead to long-term sleep debt and hormonal imbalances.
3. Respiratory Issues: Mechanism: AC units can dry out the air, reducing humidity to levels that irritate the respiratory tract. They may also circulate dust, mold, or allergens if not properly maintained.
Effects: Dry throat, nasal passages, or sinuses, leading to discomfort or infections like sinusitis.
Exacerbation of asthma or allergies due to cold, dry air, or poor air quality. Increased risk of respiratory infections, as cold air may weaken mucosal defenses.
Severity: Mild to severe, depending on pre-existing conditions (e.g., asthma) and AC maintenance.
1. Debye potentials, also known as electric double layer (EDL) potentials, describe the electrical potential difference across a membrane due to the presence of ions in the surrounding electrolyte solution. This potential arises from the interaction between charged surfaces and ions in the solution, influencing the distribution of ions near the membrane. LNP raise the Debye potentials when they are charged. This means that LNPs are more likely to interact with cell potentials.
I have been studying vials of jabs from different countrie s to see if there was any chicanery done by the manufacturers of the jabs and I have found that the ones earmarked to Israel had neutral charges on their LNPs. Some states in the USA also showed this effect. (Vermont, Mass, NJ) I believe this is why these high compliant places did not have the side effects that other zip codes had due to Debye potentials.
Recall, that due to the presence of phosphate groups in nucleotides, DNA/RNA have a negatively charged charge. RNA contains a ribose sugar which is more reactive than DNA. DNA is a more stable molecule than RNA due to its deoxyribose sugar. It contains one less oxygen-containing hydroxyl group confering this ability.
DNA/RNA are dimagnetic. During mitosis when the nucleic acids are most at risk mitochondria undergo fragmentation and are redistributed throughout the cell. This process ensures that magnetic forces from the ATPase do not affect chromosomes separation. If this process is deffective due to LNPs charges, aneuploidy and alterations in microtubule function is possible. This is also critical time in the cell because mitochodnrial fragmentation allows each daughter cell to receive a sufficient number of functional mitochondria. Specifically, mitochondria lose their connections to microtubules, allowing them to distribute more evenly and avoid being trapped by the mitotic spindle. LNPs can interrupt this process. These effects would be seen in aftermarket data. nature.com/articles/s4146…
2. Haplotypes influence uncoupling efficiency, which ties into mitochondrial processes and potentially ultraweak photon emissions (UPEs).
Here's how they connect: Haplotypes can affect the expression or function of proteins involved in the mitochondrial electron transport chain (ETC), such as cytochrome c oxidase (CCO, Complex IV). CCO plays a key role in oxygen reduction and water formation during ATP synthesis.
Variations in genes encoding CCO subunits or related regulatory proteins (e.g., due to haplotypes) alter uncoupling efficiency, where protons leak across the inner mitochondrial membrane, reducing ATP production but generating heat and reactive oxygen species (ROS).
This uncoupling therefore influence UPEs, since UPEs are thought to arise from ROS-mediated oxidation of lipids or proteins, a byproduct of mitochondrial metabolism.
Since CCO controls water creation metabolically by facilitating the final step of oxygen reduction (O₂ + 4H⁺ + 4e⁻ → 2H₂O), haplotype-driven changes in its efficiency should modulate ROS levels and, consequently, UPE intensity. Higher uncoupling might increase ROS, boosting UPEs, while efficient coupling might suppress them. This is why high latitude deaths were so high compared to equatorial deaths from COVID or the jab.
3. Regarding LNPs, if haplotypes affect CCO function and uncoupling, this would indirectly influence the cellular environment (e.g., ROS or pH) that LNPs encounter, potentially impacting their charge interactions or stability. This is why different zipcodes have different aftermarket data. I believe some of the data theft from 23andMe was used in GOF viral construction and in the creation of of LNPs and their charges. The direct charge on LNPs remains dictated by their lipid composition, but haplotypes will certainly affect it. I worry that the cabal used stolen data to build this bioweapon.
Regarding DDW, Pollack’s research on exclusion zone (EZ) water suggests that structured water near hydrophilic surfaces can develop a net negative charge due to the separation of charge, with positive ions excluded from the EZ. If DDW, with its lower deuterium content, enhances EZ water formation (as some of his studies imply through improved structuring), it could exhibit a net negative charge.
This charge would theoretically influence the electrostatic environment around LNPs, affecting their interaction with cell membranes or mitochondrial components, especially if haplotypes modulate CCO activity and water production.
It creates an ocean inside of us like we had in the womb.
That ocean is a semiconductor along with the protein semiconductors it surrounds creates light called UPEs.
The size of the ocean is stochastically linked to the spectrum and amount of photons made by mtDNA, blood, and DNA/RNA. mRNA from spike ruins water production. It creates a desert the size of MARS inside of your cells and skull and this is why it causes the diseases it does.
If you see the AM sunrise you can then use the TCA and urea cycle. = you can make the heat sink required to make the highest quality UPEs your cell needs to do all the amazing things if does.
Complete combustion of 100 gms of
FATS = 110 = 110 gms of DDW from CCO
Protein = 75 = 75 gms of DDW from CCO
Carbs = 55 = 55 gms of DDW from CCO
nnEMF/blue light force use of all glycolysis and PPP because they force all Fe to the +3 state = your running hypoxic and on the oldest metabolic pathways from the GOE that were built for more non complex life. Life did not have a Ferrari engine in their skull that get 20% of Cardiac output which needs all its hemoglobin in the +2 to carry O2 to the mitochondria of the brain who wants to run the TCA and urea cycle. This is why the brain is covered in CSF = 99.8% DDW from choroid plexus which is an ultrafiltrate of your blood.
2. Darwin cannot explain 3 things we know are true today
1. Cambrian explosion
2. The transition from a chimp to human
3. Why do primates have the same number of genes as humans yet are so different?
A longstanding debate in evolutionary biology concerns whether species diverge gradually through time or by rapid punctuational bursts at the time of speciation. The theory of punctuated equilibrium states that evolutionary change is characterized by short periods of rapid evolution followed by longer periods of stasis in which no change occurs. Despite years of work seeking evidence for punctuational change in the fossil record, the theory remains contentious. This changed in September 2022 when genomic arrays of the clade of mammals were completed. What did it show?
3. The reason evolutionary biologists were impotent to find these answers in the fossil record was that melanin from the POMC gene explained these paradoxes and was highly conserved in DNA that was stable in the mammalian tree.
The "hard problem of consciousness," introduced by David Chalmers, refers to the challenge of explaining how physical processes in the brain give rise to conscious experience, the subjective "what it's like" aspect of mental states. When you are done with #55 I will have answered every question about it.
My ideas on consciousness will push boundaries over the precipice, because they offering a profound, elegant solution to the "hard problem" patreon.com/posts/decentra…
Your World, Your Lens: You Don’t See Reality—You See What Serves You
In my manifesto, I believe, Decentralized Medicine #55 will go on the Pantheon of my top ten blogs. It might be the best one I have done because it answers questions no one has. My philopsophical transaction will shift your lens, by altering the light of UPE to change your world. You will see how consciousness was crafted by Nature and what a story it is for a Sunday AM.
What’s one thing you saw today that wasn’t what it seemed?
What’s shaping your reality today? Fear? Hope? Habit?
Your truth isn’t THE truth.
Ever wonder why you see what you see? Your mitochondria are talking, syncing light and energy to build your reality. What’s one moment today where your perception felt ‘off'?
You don’t see the world as it is—your consciousness, wired by mitochondrial motherboard and UPE-guided neural circuits, sculpts what’s useful. From Turing’s patterns to circadian rhythms, your brain’s electromagnetic roots shape your lens
Reaction-Diffusion Dynamics is the key theme in Turing’s model of morphogen gradients and this aligns with my version of how mitochondrial communication is done by electromagnetic signals. The blogs focus on mitochondrial specialization (e.g., functional diversity via quantum effects) mirrors Turing’s instability-driven patterning, where NCCs use mitochondrial UPEs and magnetic fields as morphogens to break symmetry and form brain structures (e.g., retina, cortex). Noether's and Shannon will make an appearance too.
Count on it.
Your reality? It’s coded by light and energy in your cells
Your World, Your Lens: Consciousness Shapes Reality—You See What Your Mind’s Wiring Allows.
Your Consciousness Isn’t Just You—It’s a Cosmic Circuit Board.
Your consciousness isn’t just ‘you’—it’s a mitochondrial symphony shaping your reality. What’s your lens showing you today?
2. Implications of this blog for people like @NicoleShanahan ?
My Photobiological Recursive Loop:
UPEs and Mitochondrial Activity: UPEs from Neural Crest Cells mitochondria couple with MT dynamics and circadian timing, driving mitosis and differentiation of sensory structures during neurulation. The embryo begins to focus on UPEs, which are crafted during early embryonic patterning (e.g., Wnt, FGF, BMP).
This suggests to me they are the signals may modulate UPE emission, aligning with your recursive loop. Why is it them? Because a normal embryo is 90% water. This tells me that Autism can be caused by the disruption of that three-peptide, which alters the recursive loop, or dehydration for any reason. This explains the epigenetic change in the number of affected boys from 1 in 100,000 to one in 12 boys in California.
Water and Coherence: Since the fetus is composed of approximately 90% water, which is structured into coherent domains (CDs) by UPEs, this directly enhances signal diffusion between NCCs and placodes. The photomolecular effect in water is expected to restructure water clusters, thereby optimizing sensory organ development.
Circadian Rhythms: The conserved GnRH2 and ipRGC-SCN axis (from placode/NCC contributions) link sensory development to circadian regulation, preparing the fetus for postnatal sensory integration. This is also why sex differences exist in firstborn male autists.
3. Turing’s Morphogenesis Paper
Reaction-Diffusion Dynamics: Turing’s model fits the neural plate border, where Wnt, FGF, and BMP gradients act as morphogens, breaking symmetry to specify NCC and placode fates. My photobioelectric morphogens (UPEs, magnetic fields) extend this, with NCCs using these signals to pattern the cranial sensory system.
Pattern Formation: The interplay between migratory NCCs and invaginating placodes mirrors Turing’s instability-driven patterns, with UPEs and electromagnetic fields guiding the spatial organization of the pituitary, eyes, nose, ears, and ganglia.