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?Image
2. How does it all fit into today's current events? forum.jackkruse.com/threads/ww1-th…Image
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.Image
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.Image
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.Image
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.Image
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.Image
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.Image
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.Image
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. @KONCRETEImage
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.Image
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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. Image
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.Image
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. Image
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.Image
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. Image
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"Image
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.Image
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.Image
20. What was in the COVID jabs? Simian virus 40 promotor. Image
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More from @DrJackKruse

Jan 28
1. Today's lesson from my forum is on hyperhydrosis and dysautonimia.

QUESTION: Hi everyone,

Starting this thread to document my improvements or lack thereof, as I get closer to the Equator and further away from nnEMF.

My issue is a form of Dysautonomia driven by a small gain of function mutation in the gene encoding for Nav1.7.

The results is a persistent Na+ leak in the neurons where Nav1.7 is expressed, resulting in hyperexcitability of these neurons.

This hyperexcitability leads to the following symptoms: sympathetic overactivity, hyperhidrosis, gut hypersensitivity, more prone to visceral anxiety, bronchoconstriction, etc.

I know the decentralized medicine perspective says this is an environment problem and not a genetic problem.
But I'll only be able to confirm this once I get my environment right and get rid of these symptoms.

Best,
Alex

How can my neurons help Alex?Image
2. ANSWER:
Relationship Between Hyperhidrosis and Dysautonomia

Hyperhidrosis is frequently recognized as a specific symptom of a broader autonomic dysfunction.

In cases involving the upper neck:

1. Localized Sweating: Irritation of the sympathetic fibers around the vertebral artery often causes sweating or flushing on only one side of the face.
2. Systemic Dysautonomia: If the compression affects the brainstem's ability to regulate the whole body, you might experience more generalized symptoms like heart palpitations, temperature dysregulation, or "drop attacks" (sudden weakness).
3. Other relationships to be explored are found below

A. Vertebrobasilar Insufficiency (VBI): The bony bridge can compress or "kink" the vertebral artery, especially during head rotation. This reduces blood flow to the brainstem, which houses the primary control centers for the autonomic nervous system. This can manifest as dizziness, fainting (syncope), and nausea, all signs of dysautonomia.

B. Barré-Liéou Syndrome: This is a specific cluster of symptoms caused by irritation of the posterior cervical sympathetic chain (the nerves that control "automatic" functions like sweating and heart rate) due to cervical spine issues. Symptoms often include unilateral facial sweating, flushing, blurred vision, and ear ringing (tinnitus). Tinnitus brings the link to melanin dysfunction in the stria medullaris as I have laid out painstakingly on 7 Patreon blogs. It signifies an nnEMF etiology to the Hyperhidrosis and dysautonomia.

C. Trigemino-Autonomic Activation: When the C1 nerve or the vertebral artery is irritated by the ponticulus posticus, the signal is processed in the Trigeminocervical Complex. This can trigger a "reflex" in the autonomic system, leading to craniofacial hyperhidrosis (sweating on the face/forehead), nasal congestion, or eye-watering. This can also be stimulated by demyelination in this region by melanin POMC defects, DHA defects in the central retinal pathways, or polarization toxicity that affects the nerve complex that links these two disease. Both, hyperhidrosis and dysautonomia are located in two distinct but interconnected systems: the Central Autonomic Network (CAN) in the brainstem and the Peripheral Sympathetic Chain in the neck. Hyperhidrosis in this scenario is typically a "positive" neurological phenomenon (overactivity) caused by irritation of the Superior Cervical Sympathetic Ganglion (SCG) and the Periarterial Carotid Plexus (lots of POMC).Image
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3. ANSWER CONTINUES

The broader "dysautonomia" (dizziness, heart rate changes, nausea) stems from a defect in the Lower Brainstem, specifically the Nucleus Tractus Solitarius (NTS) and the Ventrolateral Medulla. These are the primary control centers for blood pressure and heart rate, located in the medulla oblongata of the brainstem. When these brainstem centers are deprived of oxygen-rich blood, like we see when Fe is forced into the +3 state over the +2 state, they fail to regulate the autonomic system correctly. This is why nnEMF can cause this syndrome. This results in the "mismatch" symptoms of dysautonomia, such as postural dizziness, syncope (fainting), or "drop attacks" where the legs suddenly give out.

Because these symptoms are often positional, it is highly recommended to speak with a radiologist specialist about a Digital Motion X-ray (DMX) or a CT Angiogram to see how your vertebral artery behaves when you move your neck.
Read 16 tweets
Jan 22
1. The phrase "absence of evidence is not absence of effect" is a powerful reminder in science: just because something hasn't been definitively proven (or detected) doesn't mean it has no impact. This is especially relevant when paradigms resist change, funding biases exist, or long-term/low-level effects are hard to study. Alfred Wegener's story powerfully illustrates this because his continental drift idea was dismissed for decades due to lack of a plausible mechanism, yet it was fundamentally correct, vindicated by later evidence like seafloor spreading and plate tectonics.

The Nuance on Historical Cases

Wegener/Plate Tectonics: This is solid and uncontroversial because mainstream geology now fully embraces it. Keep the dramatic narrative, but note that the delay stemmed partly from genuine scientific gaps (no mechanism until mid-20th century oceanography), not just malice.

Robert O. Becker and EMFs: Becker was a respected pioneer in bioelectromagnetics (e.g., bone regeneration via electrical signals). His work on ELF EMFs faced pushback, including funding cuts and professional isolation after public criticisms (e.g., his 1977 60 Minutes appearance and conflicts with NAS figures like Philip Handler). Andrew Marino's Going Somewhere (his autobiography) details this as industry/military-influenced suppression. Current evidence on EMFs (e.g., ELF from power lines or RF from wireless) shows mixed results: some studies link exposure to oxidative stress, DNA damage, or neurological effects, but major reviews (e.g., IARC classifies ELF magnetic fields as "possibly carcinogenic" Group 2B based on childhood leukemia associations; RF as 2B). No strong consensus for widespread cancer causation at typical exposure levels, though oxidative stress mechanisms are actively researched and some reviews find biological effects. Update to reflect this: suppression claims are debated, but Becker's concerns about non-thermal effects persist in ongoing debates.

Bernice Eddy and SV40: Eddy identified SV40 contamination in early polio vaccines (1955–1963, affecting ~98 million doses, 10–30% contaminated) and linked it to tumors in animals. Her warnings faced institutional resistance (e.g., lab disruptions). IOM/National Academies (2002) concluded biological evidence shows SV40 is oncogenic in animals and detectable in some human tumors (e.g., mesothelioma), but epidemiological studies find inadequate evidence for a causal link to increased cancer rates in exposed populations. Modern data around COVID jabs now show proven causal association with human turbo cancers; SV40 has been found in vaccines post-1963 as the paper below shows.Image
2. Confirmed on SV40 Promoter in COVID mRNA Vaccines

Independent labs, including Kevin McKernan's team, have repeatedly detected residual plasmid DNA, including the SV40 promoter-enhancer-ori sequence, in Pfizer vials (not Moderna, or at much lower levels). This is no longer fringe or unpublished:

A 2025 peer-reviewed paper in Autoimmunity (Speicher, Rose, McKernan et al.) quantified it in Ontario-distributed vials: SV40 promoter-enhancer-ori at 0.25–23.72 ng/dose in Pfizer samples, with total residual DNA exceeding FDA/WHO limits (10 ng/dose) by 36–153-fold via fluorometry (after adjustments). qPCR showed some lots exceeding limits specifically for SV40 elements by ~2-fold. Oxford Nanopore sequencing confirmed fragments up to 3.5 kb, likely encapsulated in LNPs (lipid nanoparticles), raising transfection/integration concerns.
Earlier 2023 preprints (now cited in peer-reviewed work) and Buckhaults' 2023 South Carolina Senate testimony aligned: billions of DNA fragments per dose, including SV40 promoter from manufacturing plasmids (different from trial batches).
These findings appear in regulatory discussions (e.g., CDC ACIP slides referencing them as safety uncertainties) and critiques of manufacturing scale-up.
Buckhaults (a cancer genomics expert, who was not anti-vax before this finding has described the promoter as a "volume knob" for expression (originally for antibiotic resistance in plasmids), but noted theoretical risks like genome integration or p53 interference.

He stressed in 2023 that no proven cancer causation was present then, but he called for sequencing in affected individuals.
Speicher, Rose, McKernan et al. proved it so now it is a GIVEN.

Regulatory bodies (FDA, EMA, WHO, TGA) acknowledge the SV40 promoter was used in production plasmids but insist residuals are below safe thresholds in approved batches, fragmented/non-functional, and no epidemiological signal of harm (e.g., no genome-altering or cancer surge in billions of doses). We now know this is also false.

They differentiate: this is not the full SV40 virus (as in 1950s polio contamination) or its oncogenic T-antigen.

Ties to Cancer / "Turbo Cancer" Signals

The January 3, 2026, Oncotarget review (Kuperwasser & El-Deiry) compiles 69 publications (2020–2025), including 333 case reports/series across 27 countries of post-vax cancers (recurrences, rapid progressions called "turbo" patterns), plus larger cohorts showing associations (e.g., thyroid, colorectal, lung). It proposes mechanisms like immune shifts disrupting tumor dormancy but stresses these are signals, which needing rigorous follow-up because it is clear now Dr. Fauci and BigHarma lied. The FDA and CDC failed to police the public health. They are still harming the public now with their stance on the COVID jab for humans.

The journal reported DDoS cyberattacks disrupting access around publication, possibly linked to PubPeer criticism, fueling suppression claims (reported to FBI).

There is significant signal in the data that now proves there is a likely causal effect from DNA incorpation of contaminated genetic elements fueling "turbo cancers" from vaccines or SV40 fragments. The centralized major bodies who are incentivized by NIH, DOD, DARPA and BigHArma funding contiunue to float the narrative that they find inadequate evidence for mechanism. This is the only reason "turbo cancer" lacks formal recognition in centrlaized circles.

But the pattern in COVID jab biology echoes Eddy/SV40: early warnings dismissed, animal data ignored, epidemiological gaps persist. Quantum biology angles (subtle, hard-to-measure effects like DNA interactions) could explain why direct proof lags.

This reinforces my original point: science doesn't always self-police effectively when monopolies (corporate, funding, paradigm) are at stake. McKernan/Buckhaults' work faced initial resistance but gained peer-reviewed traction shows the truth rising slowly, as with Wegener.Image
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3. Strengthen the Core Thesis of how centralized science lies

ABSENCE OF EVIDENCE IS NOT ABSENCE OF EFFECT

Wegener's body buried beneath the snow. His companion had wrapped him carefully, marking the grave with skis standing upright in the ice—a memorial to a man the world had refused to believe.
His theory remained buried with him. Dismissed. Forgotten.
For three decades.
Then, in the 1960s, scientists discovered something extraordinary beneath the ocean floors: mid-ocean ridges where new crust was continuously forming. Magnetic patterns in rocks that recorded Earth's history. Evidence of massive tectonic plates shifting beneath our feet.
Everything clicked.
Wegener had been right all along.
The mechanism he couldn't explain was plate tectonics—giant slabs of Earth's crust floating on molten rock, colliding to build mountains, separating to create oceans, reshaping the planet over millions of years.
Every prediction Wegener made was validated. Every mockery he endured was proven wrong.
Today, his name appears in every geology textbook. Students learn about Pangaea in elementary school. Scientists use his theories to predict earthquakes, understand volcanic activity, and trace the history of life on Earth.
But Alfred Wegener never saw his vindication.
He died alone in the Arctic, believing in something he couldn't prove, ridiculed by the very community he was trying to advance.
And yet he kept going. Not for fame. Not for approval. But because when you see the truth, you can't unsee it.
The continents were moving. The Earth was alive beneath our feet.
He saw it when everyone else was blind.
Alfred Wegener's story is a reminder that truth doesn't need permission to be true. That the most important discoveries often come from those willing to be wrong in the eyes of the world—and right with the universe.
Sometimes the bravest thing you can do is look at what everyone else sees and ask a question no one else dares to ask.
Sometimes the most powerful legacy isn't the one you live to see.
It's the one that changes everything after you're gone.
Alfred Wegener—the man who saw the Earth moving, long before the Earth was ready to be seen.Image
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Read 10 tweets
Jan 18
1. Today's lesson comes from my forum.

Dr. Rob asks me the following:

" Jack, based on your recent cancer blogs and critique of Seyfrieds Metabolic and Levin‘s bioelectric models - it’s clear your photo bioelectric framework is correct.

A Photo-Bioelectric Coordination Hypothesis of Cancer

I propose a framework in which cancer represents a system-level collapse of photo-bioelectric coordination, rather than a primary genetic, metabolic, or bioelectric disease. In this model, organismal integrity depends on a coordinated Organ Trinity:

The Organ Trinity: Light, Shadow, and Darkness

In health, organismal integrity depends on coordination between these three central organs, each operating in a distinct but complementary energetic mode:

The hypothalamus functions as a photonic interpreter. It translates environmental light into biological time, establishing circadian phase and temporal order. This is the domain of Light - timing, anticipation, and synchrony.

The liver acts as a photoelectric buffer and decision hub. It integrates metabolic load, redox stress, toxins, and fuels, determining whether the organism should proceed, pause, or shift strategy. This is the domain of Shadow - adaptation, buffering, and reversible retreat.

The heart provides continuous charge circulation. Its uninterrupted electrical and mechanical activity sustains organism-wide coherence and regenerative safety. This is the domain of Darkness—ongoing work, continuity, and renewal.

These organs are coordinated through nested signalling layers: photonic information (including circadian light and UPEs), photoelectric transduction (via cytochrome c oxidase, heme proteins, and melanin-like systems), and organism-wide DC bioelectric fields consistent with Becker's work on the perineural system and endogenous DCs..
2. Dr. Rob's questions continue.....

"Photons as Primary Biological Drivers

This framework explicitly positions photons as the primary informational input in biology, with bioelectricity emerging downstream of photoelectric transduction. Causality is hierarchical: photons → photoelectric transduction → bioelectric fields → biochemistry → genetics This ordering reflects the necessity of temporal and energetic coherence before molecular signalling can be meaningfully interpreted. Biology is therefore not merely bioelectric, but photo-bioelectric, with light establishing phase, coherence, and permissible state transitions.

The Liver as a Central Photoelectric Organ

This hypothesis emerged from recognising an architectural asymmetry: the liver is the only primary human organ with complete regenerative capacity and the dominant site of fermentation and alcohol metabolism. More fundamentally, it possesses the densest photoelectric infrastructure in the body, high concentrations of heme proteins, melanin analogues, extensive mitochondrial mass, and strong UPEs, suggesting a unique role in maintaining coherence under photonic and metabolic stress. Rather than viewing fermentation as a pathological detour, this framework treats it as a Shadow state, a stress-buffering, redox-preserving fallback when photonic or respiratory coherence is threatened."Image
3. Dr. Rob continues....

"Cancer as Photo-Bioelectric Coordination Failure

Three Questions Every Cell Once Asked:

In a healthy organism, cells continuously receive answers to three implicit questions:

When should this happen?
(answered by photonic timing via the hypothalamus)

Should this happen?
(answered by hepatic buffering and redox decision-making)
Can this happen safely?
(answered by continuous charge flow and regenerative capacity)
When cells can no longer answer these three fundamental organism-level questions, they default to autonomous survival programs."
Read 12 tweets
Jan 15
How? @MitoPsychoBio is currently trying to sell the centralized paradigm idea that mitochondria are just a energy powerhouses. He is right, but for the wrong reasons. He stays in biochemistry because it is all he understands. The answer is in physics of light.

Mitochondria make light in the form of UPEs.

To understand the connection between electromagnetism and the weak nuclear force, it helps to think of them as two different "dialects" of the same original language. While they look and act differently today, they were once a single, unified
electroweak force.

1. The Core Connection: A Shared Origin

Physicists discovered that if you look at the universe at extremely high temperatures, like those just after the Big Bang, electromagnetism and the weak force merge into one. In this high-energy state:
They become identical Messengers: All the particles that carry these forces (the photon for electromagnetism and the W and Z bosons for the weak force) were originally massless and indistinguishable from one another.

The Big Split: As the universe cooled and temperature pressure and energy changed, it underwent a process called spontaneous symmetry breaking. This is similar to water freezing into ice: the "fluid" symmetry of the water is lost as it locks into a specific crystal structure.

2. Why They Seem Different Now
The reason we experience them as separate forces today is due to the Higgs Field, which acts like a "thick syrup" pervading the universe.

The Weak Force (Heavy): The W and Z bosons interact strongly with the Higgs field, which gives them a massive "weight." Because they are so heavy, they can only travel tiny distances (less than the width of an atom), making the weak force extremely short-ranged in Nature.

Electromagnetism (UPE Light): The photon does not interact with the Higgs field at all. It remains massless and can travel across the entire universe at the speed of light, which is why we can see stars billions of light-years away.

3. A Simple Analogy
Imagine a heated magnet:
At high heat: The magnet loses its north-south orientation. All directions look the same; it has perfect rotational symmetry. This is the unified electroweak state.
As it cools: The magnet suddenly "chooses" a direction and develops a north and south pole. The original symmetry is broken, and two distinct "sides" (forces) emerge.

What is UPEs major target in a cell? MELANIN. Melanin is a magnet because it has unpair electrons. Picard forgets the basics because of biochemical myopia.

Picard will soon learn when he learns some physics from his wife that mitochodnria acts as lenses in tissues with respect to light running optically around, in, and through them.

He will soon realize that my idea that mitochondria polarize internal UPEs to maintain "efficiency" suggests a highly specific optical environment (topology). His wife can tell him that the Nobel Prize for topology was given in 2016. Blue light from any man made source is polized circularly. Look it up. That is how they engineered it.

Why Picard needs to learn physics if he really wants to be a mitochondriac? The physics of polarization is linked to the weak force via Parity Violation. Because of this, exogenous CPL in the form of blue light should act as a "spoiler" if its handedness or energy levels conflict with the cell's internal chiral "tuning," potentially forcing the biological topology into a less efficient state through asymmetric photochemical induction.  

Picard does not seem to remember that CPL's are so specific they are now being used to evaluate the central retinal pathways and brain for misfolded proteins in human disease. Fact check me Savages.  

Right now centralized medicine seems to have no idea protein misfolding is caused by the diagnostic tools. CPL interacts so specifically with chiral biological structures, it is being used in 2026 as a non-invasive tool for detecting diseases like Alzheimer’s, which involve changes in the "handedness" of protein plaques. You should be aware of their myopia. I'm challenging Martin to challenge his own right now.

The tie to the evolution of melanin is not just elegant but pivotal in understanding the modern disease landscape, especially when one considers how scale enters the equation with respect to the electromagnetic force. My emphasis on how electromagnetism's effects amplify dramatically at nanoscale distances flips the script on "weak" external inputs like blue light: What seems subtle globally becomes a destructive force internally via amplified UPE cascades in tissues leading to photobio-electric scarring and dessertification. The mechanism of blue-light disruption is well documented (via chronodisruption, melanopsin dysregulation, and ROS amplification in studies from the 2010s–2020s), and in a 2026 context, emerging biophotonics data only strengthens my ideas. I'm doing playing small ball with the smooth brainers. Time to step on the gas.Image
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2. For the biochemistry food retards: Can you make melanin or dopamine if the parity violation in polarized life destroys your pool of L-tyrosine or L- phenylalanine due to polarized blue light exposure?

Look at the dam slide, top line below.

This perspective is a masterclass in decentralized thinking where the surface chemistry (eye/skin as photonic interfaces) trumps internal biochemistry because scale dictates electromagnetism's dominance.

UPEs aren't mitochondrial noise; they're nanoscale lasers signaling via polarization, with melanin/dopamine as the evolved decoder. Modern disruptions (blue/nnEMF) exploit this by amplifying weak inputs into destructive cascades, explaining disease epidemics as "optical mismatches" since GOE. GAME SET MATCH MY SAVAGES.Image
3. While the weak force provides a constant "hidden" bias, Circularly Polarized Light (CPL) acts as a powerful external "wand" that can either reinforce or override it. This is how man made light is engineered by DOD/DARPA design (MKULTRA)

Asymmetric Photochemistry: CPL from star-forming regions can selectively destroy one handedness of a molecule while leaving the other intact. This has been demonstrated in experiments with amino acids and extraterrestrial ice analogs.

Interaction with PVED: If CPL and the weak force's PVED bias point in the same "direction," they can work together to amplify homochirality much faster. If they oppose each other, the stronger environmental factor (often CPL in high-radiation space environments) determines the final topology.

Amplification Mechanisms: In 2026, researchers are studying how tiny initial biases (from either CPL or PVED) are magnified through "autocatalytic" networks, where a molecule acts as a template for more of itself, eventually leading to 100% of one handedness in living systems.

Picard love affair with Levin needs to END. Logic is defined by light in the system not bioelectricity.Image
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Read 8 tweets
Jan 12
Dr. Morse has zero clue what ultrasound does to water in a tendon over time. If he did he would not help you facilitate your future torn Achilles tendon. If you want prevention do not screen. Walk on a beach with your feet in the water every AM, begin using grounding shoes, and use the abscopal effect of sunlight on your skin to increse the piezo electric and flexoelectric strength of solar photons to strengthen your tendons and joints.

You do not have to come to El Salvador to see me. I offer you this Rx here on X for free. You can asked Adrian Peterson, Drew Brees, or Cam Akers. We use biophyscis and quantum biology to help our trainers and athletes.

In centrlaized medicine where ultrasound screenings are used this is what they do not tell you: Using conventional orthopedic management most of these injuries requiring 9–12 months on average. See Dan Marino. Achilles tendon ruptures are severe injuries in the NFL, with historical return-to-play (RTP) rates around 60–70% and typical timelines of about 11 months for those who do return.

The first person who used decentrlaized ideas was Jerry Rice for his ACL. See how that went. He came back in same season. See TO. Broke his leg in season and played in SB that same season.
See AP.
Tore his ACL and embraced the suck of decentralized ideas and ran for 2000 yds the next yr. See 2012 T Suggs. Tore his Achilles and came back in 6 months to play in the last SB the Ravens won with Harbaugh.

Tom Brady began to use naked sunbathing to fuel his play to 47 yrs old after a KC Safety took his ACL out. These are the things centralized medicine has made fun of at your expense. Aaron Rogers uses decentrlaized medicine to come back from his ACL and is playing tonight. The media and retards made fun of his use of cold and darkness with him walking the beach in malibu as he came back at over 40 yrs old. That was a very un- Marino think Aaron did a few years ago.

Do you want to be like everyone else and do ultrasounds on you achilles or do you want to put the extra in ordinary to do what the few in the NFL have? Embrace the suck of Nature to come back fast.Image
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2. Let us ask the question Dr. Morse is too ignorant to raise, namely, what are the effects of using ultrasound on coherent domains in water? It is well established in the literature that for collagen to keep its piezo and flexoelectric abilities to performs it must be well hydrated by CCO from heme proteins. So what does screening ultrasound do to the collagen matrix in the Achilles based on what is known?Image
3. Ultrasound used in medical offices is considered by water researchers to be high intensity. Did you know this? I know the good doctor Morse doesn't because he has never read a water journal in physics in his life. If he had, he'd never have invited anyone to Miami to use a high intensity ultrasound machine to screen them. WHY?Image
Read 15 tweets
Jan 6
2. George H.W. Bush ws remembered in history books written the CIA cabal as the president who oversaw the collapse of the Soviet Union. This is horse shit but he did have another major foreign policy achievement that is absent from the history books authored by the CIA.

He was THE KEY champion of free trade and a key architect of globalization and sustaining the Deep State. His legacy is now in danger and many of his family have serious criminal problems since Maduro is out of VZ were the secrets are.

Venezuela wasn’t our enemy and never has been. The cabal controlled CIA were the real enemy in Venezuela.

Free trade was a purposeful narrative controlled by the shadow government. It was a convincing strategy at the time, and it garnered support from many Americans who believed in a more “fair” trading system worldwide. Another bush Deep State Coup against America.

Bush signed NAFTA ONE month before leaving office, and he said it would become a “model” for future trade agreements.

What is was, was just another CIA template to steal taxpayer time and money.​ You bought the CIA psyops chief and all your followers should know you are a shitty diagnostician.Image
3. NAFTA was intended to lift old tariffs, duties and trade barriers, in order to increase trade.

What has DJT reinstalled in his first year in the second term before he went into VZ?

TARIFFS.

This is why the DEEP STATE hates DJT.

This signals to them that DJT the CIA is the enemy of the people of the USA.

Why did the shadow government based in intelligence, controlled by Bush, want to increase trade to Mexico and Canada?

Barriers are the key to H.W. BUSH and Jeb Bush plan.

Why did Bush family cartel members lift all those barriers?

They learned the game from Prescott Bush during the time he hid Nazi money in WW2.

Was it about tariffs, or was it about the free “flow” of goods? What was going to be allowed to “flow freely?”

These goods from NAFTA countries would be declared “National Goods” and be free from state or local government control.

Why is that process a big deal, chief?​

​CENTRALIZATION allowed CIA control of the flow of goods in VZ.

Why would limited government control over goods traded between Mexico, the U.S. and Canada be so important to the shadow government controlled by the CIA in VZ?

I’ll ask the question again.

Was NAFTA just about free trade or was it a precursor to setting up the largest drig operation and money laundering scheme on Earth for the CIA and Deep State?

Who were the leaders that signed the NAFTA trade deal?

The three leaders were George H.W. Bush, the Canadian Prime, Minister Brian Mulroney and Mexican President Carlos Salinas de Gortari.

Mexico was key in understanding the psy-ops design. You failed at this class.

It was all about allowing the free flow of drugs into the US from the Mexican Cartels to control Americans and dumb them down and steal their assets. That has been going on since George H Bush left office.
4. Who was Carlos Salinas de Gortari?
​He was Mexico’s 60th president and leader of the controlling political party in Mexico called the Institutional Revolutionary Party. (PRI)
He was a very powerful politician and became very popular with his economic reforms, including NAFTA.

What else did he do besides NAFTA?
​He privatized everything he could in Mexico. That facilitated centralized control by the few in his country. This is how we got the lattest robber barrons.

President Salinas oversaw the biggest privatization program in Mexico, and it was directly connected to NAFTA.
Privatization didn’t create competition at all. It just transferred ownership of the monopolies from the government into private hands.

The year before the NAFTA agreement, Mexico only had two billionaires. When Salinas left office, there was 28 billionaires. That was not just a coincidence it was designed by the CIA banking cartel on Wall Street. Those 28 billionaires became the new robber barons of globalization. Carlos Slim was one of these guys in telecom and Big Tech.

There is a Bitcoin link. Raúl Salinas de Gortari, Carlos's brother, loaned Ricardo Salinas Pilego 29 million to buy TV Azteca during his presidency, leading to later investigations and public scrutiny.

This is why I have always been leary of Salinas role in Bitcoin in Mexico.

Go and listen to his Bitcoin story he always talks about 1994. Know your enemies bro by knowing their history. .Image
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