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

Aug 21
A couple of points: Not all human cells have mtDNA. See adult blood cells. This is a big deal when you consider their absorption spectra. 200-600 nm light with a sharp cut-off. Also, blood still transforms energy into UPEs. And since blood fills 20% of our CO to the CNS, this also has implications. The retina and gut increase their blood flow with light use and feeding. Feeding is a light-based phenomenon since all food webs link back to photosynthesis.

In humans, light stress does not force mitochondria to react exactly the same way as infection (no ATF4 surge, different folate handling), but there are partial overlaps in ISR activation, 1C remodeling, and mtDNA signaling.
This suggests UV light acts more as an external folate depleter for DNA protection/photorepair, while infection is an internal ATF4-orchestrated defense. If environments lack natural light controls (as in modern human life), it should exacerbate mismatches in folate biology. For deeper dives, I'd recommend reviewing the ATF4-UV papers for experimental details.

Folate as a Light-Responsive Switch: My patreon has made this point over and over again, natural folate (not folic acid) is photosensitive, degraded by UVB, and shows seasonal lows in summer (higher at low latitudes, with gender differences showing men have lower levels). This would act as a "switch" for mitochondrial/genome control, linking to melatonin/tryptophan pathways and neurotransmitter synthesis (e.g., serotonin, dopamine). In low-light/artificial blue light environments (e.g., indoors), folate stability increases unnaturally, disrupting methylation/DNA synthesis and contributing to diseases like Alzheimer's, Parkinson's, or diabetes (via melanin quenching loss and superoxide buildup). People with MTHFR and COMT defects are supersensitive to ALAN and a LACK OF SUNLIGHT. This is echoed all throughout my decentralized photo-bioelectric thesis: light refines folate via photosynthesis/food webs, but artificial setups bypass this, leading to transgenerational effects.

No Seasonal/Light Controls: absent natural light cycles (e.g., constant artificial light), retinal/CNS signaling should be expected to dysregulate—e.g., excess folic acid fortification (since 1996 in North America), which overloads 1C pathways, causing cognitive haze, sleep issues, or neural migration problems in lit environments. This photonic effect is completely missed in centralized medicine and is really missed in functional medicine, which pushes for excessive folate use with SNPs. These people need more sun and less ALAN, not drugs.

Black Swan Mitochondriac View: Melanin (from UV-absorbing aromatic amino acids) quenches mitochondrial superoxide, protecting against neurodegeneration. Blue light destroys melanin and heme proteins, amplifying risks from ALAN and a lack of sunlight which aligns perfectly with UV's mitochondrial stress but without the adaptive folate restriction seen in infection.

Now the picture is full. patreon.com/posts/decentra…
2. Why is this tweet important to the jabbed? If you follow the work of @Kevin_McKernan you'll find in his blogs many mentions of pseudouracil and jab injuries. Then you look at my blogs on jab repair, and you'll notice I recommend Tropical relocation as the best risk reduction for the compliant. WHY?

Did you know that in humans, UVR depletes folate in skin and blood, inducing S-phase arrest, affecting uracil misincorporation (frame-shift mutations), and sensitizing apoptosis in keratinocytes. This isn't "damage" but a permissive environment for seasonal phenotypic changes, e.g., increased melanin production to protect folate stores. When you understand the photorepair mechanism, you will see this is how humans can block the DoD and BigHarma death mechanism from uracil replacement induced by the jabs. @MdBreathe None of the COVID experts have this sophistication. They are still pushing detox answers when it is crystal clear that redox biology is the path for the Savage trying to stay alive and away from disease.Image
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3. Individuals with MTHFR C677T (thermolabile variant) are indeed supersensitive to light/folate fluctuations, as the mutation impairs folic acid conversion to 5-MTHF. High folic acid may select for this allele evolutionarily, acting as a "genetic time bomb" by promoting unmetabolized buildup and altering DNA/RNA biology.

People who have this SNP and took the jab have no choice but to move. If they do not, they will be taken out to Taper the Ponzi. This variant requires higher folate for stability, making carriers vulnerable in low-UVR (winter/indoor) settings, where blue light further degrades melanin (a superoxide quencher), exacerbating mitochondrial stress.Image
Read 5 tweets
Aug 19
If Einstein was correct that energy = mass times the speed of light squared (E = MC2), then how did biology make all life from that simple equation? As I looked up, the sun hit me in my eyes. I realized the link, right there. I had to reverse Einstein’s equation to see how life made sense of the chaos on our planet, to create life from it. E = MC2 is a simple math equation using simple variables we all know.
Truth Bomb #2: Life is energy and energy is life according to this equation.
It also implies that the equation can also be reversed mathematically. The “Commutative Laws” say you can swap numbers over and still get the same answer. A + B = B + A. Biologic sciences have pretty much ignored E = MC^2 for much of the last 108 years since its discovery. It has been felt to be the domain of subatomic physics and of theoretical physics, and astronomy. Physicists and chemists have always read Einstein’s masterpiece equation from left to right. This helped them explain the massive power generated from the nuclear fission of atomic blasts. As a surgeon, I realized there is were no nuclear explosions occurring in cells to generate energy. I reasoned, biology could not use the reaction that way, so life had to find another way to do it. I thought, that maybe, life at its origin on the chaotic Earth, sought order from the environments it had to endure to survive. If that was correct, then all biology must start with the speed of light, squared and not with energy. I felt I had to reverse Einstein’s equation in my head to figure the riddle out. It made sense because today we know all life makes energy from the sun or from electrons in our mitochondria. Plantlife uses the photons or electrons of the sun to make its energy efficiently. Animals use electrons to make fuel in the mitochondria in the form of ATP.
The M, the ‘mass’ part of the equation brings in the elements of space/time and gravity from physics. This is a topic biology rarely deals in. This is where the riddle got complex for me. This implies the way the mitochondria account for energy has to include a very precise timing procedure as a part of energy generation. I knew from mitochondrial biology that is precisely what the “Rolex” in our head does at the SCN by responding to the magnetic field of the Schumann resonance of the Earth.
But there is more.
Food is information of light from the sun. It is also energy. This means that info and energy are linked. It turns out they are linked via the concept of mass.
Shannon took the vague concepts of information and pinned them down to what its essence was all about.
He asked what was the minimum requirement needed to create a message that could still be deciphered well.
The equation he came up with looks identical to Boltzmann's equation for entropy. This means Information truly links to thermodynamics.
Boltzman gave us the statistical explanation of the second law of thermodynamics. In 1877 he provided the current definition of entropy,
In 1948 Shannon figured this out by mathematically learning how to measure the information in the messages
Shannon realized that the quantity of the message had ZERO to do with its true meaning.
Physicist John Wheeler extended Shannon's ideas further.
Wheeler tells us every particle in the universe emanates from the information locked inside it.
My idea at my KLC clinic: This idea has massive implications for mitochondrion who deal exclusively with light, electrons, and protons in cells.
Wheeler’s ideas have been expanded recently by Vopson (dark energy non-believer)
His paper says that not only is information the essential unit of the universe but also that it is energy and it has to have mass.
To support this claim, he unifies and coordinates special relativity (1905) with the Landauer Principle (1961)
Landauer predicted that erasing even one bit of information would release a tiny amount of heat, a figure which he calculated = mtDNA is a heat engine
If information is energy, Information, once created has to "finite and quantifiable mass."
This connects information directly to energy. E-mc^2
When information is lost in the system there has to be a change in mass in the system..............
These ideas fueled the EMF 2 blog post at jackkruse.comImage
2. It amazes me how ignorant the paradigm is about AM sunlight. AM sunlight is filled with high intensty red light and a smaller amount of blue light. This is why the color temperature of AM sunlight at sunrise is around 1600K and it is 16,000 K at sunset. High intensity red light in the AM is the light that Nature uses to stimulate testosterone release in men. UV light is a potent "off switch" for testosterone action in the blood. It amazes me that this PEER reviewed article has no clue that AM SUNLIGHT is the circadian controller of testerone level in MEN.

They want to use fake light.........to do the job of the sun.
Ridiculous.

The use of light therapy dates back to ancient civilizations, going as far back as the ancient Egyptians and Indians, who used sun- light (heliotherapy) for healing and promoting health. The therapeutic use of light energy was more fully appreciated in the late 19th century when a Danish physician-scientist, Niels Ryberg Finsen, demonstrated the benefits of red and blue light in the treatment of lupus vulgaris and was recognized with the 1903 Nobel Prize in Medicine and Physiology. In 1960, the L.A.S.E.R. (Light Amplification by Stimulated Emission of Radiation) by Theodore Maiman was invented, based on theoretical work by Albert Einstein in 1917.

This brought renewed attention to the therapeutic light energy field. The monochromatic, coherent, and collimated nature of lasers led to immediate interest in their biologic effects. In 1967, Endre Mester, a Hungarian physician-scientist, reported that low-dose laser treatments were capable of promoting wound healing and hair regrowth in mice. He termed this phenomenon photostimulation and went on to demonstrate the efficacy of this treatment in human patients with skin ulcers. medicalnewstoday.com/articles/31296…
3. When a human lives in a poor environment loaded with Blue light and nnEMF it stimulates a type of cell death called 'ferroptosis'. Do you know about it? Most gurus have never even herd of it. This is why you must be careful who you allow to pack your parachute.
Ferroptosis is defined by the iron-dependent accumulation of lipid peroxides when heme containing photoreceptors undergo damage. Most people have no idea that this occurs in the blood (catalase), mitochondrial cytochromes, and th eP450 system. All of them containing heme (iron based) proteins that work with light. Ferroptosis is associated with the abnormalities I look for in peripheral blood smears at Kruse Longevity Center and it is genetically (DNA/mtDNA) and biochemically distinct from other forms of programmed cell death such as apoptosis, necrosis, and autophagy. It is linked to why many gas anesthetics are linked to neurotoxicity in people with neurodegeneration. It also is linked with people who are floxxed and have many other mitochondrial redox linked diseases.
It appears this new mechanism is driven by downstream inactivation of glutathione peroxidase 4 (GPX4, Yang et al., 2014). Peroxidase enzymes are ALSO ALL HEME containing proteins. I believe the fluoride in the inhalational or prescription drugs is ONE of the proximal cause of the iron-dependent accumulation of lipid peroxides because it causes a dielectric collapse in the metabolic water around these proteins in mitochondria. I also think this leads to melanopsin dysfunction in the circulatory system where the most heme iron-containing proteins exist in man. The tell tale sign is when retinol levels in the plasma rise sharply because the Vitamin A derivative is running free destoying photoreceptors as it goes.
The second critical spot they are found is in the mitochondrial membranes of man. This has not been studied as far as I can tell in 2019. The normal dielectric constant of water is 78 in bulk water but it has been shown to be 160 in metabolic water or EZ. I have been waiting for papers to link melanopsin dysfunction to a falling dielectric constant in the anesthesia literature but no luck on that so far. I strongly believe these mechanisms are linked. This is why Vitamin C by the IV route can help cases like this. It will not work by the oral route.
Mitochondrial cytochromes are all heme-containing lipid proteins. This would cause acute colony failure of the photoreceptors there. I bet it would alter catalase in the cell as well which quenches free radical signal H202 as well. Catalase is another heme-containing protein. All heme-containing proteins seem to be red light chromophores as well. Hemoglobin is the main red light chromophore porphyrin in our blood. Hemoglobin has a strong ability to absorb light between 250-600 nm. UV light spectra go from 250-399nm in man. The word porphyrin is derived from the Greek word which stands for purple. Purple light is UV light color in the solar spectrum. Again here you see the link back to UV and IR light in these disease mechanisms. B12, folate, melatonin, riboflavin, serotonin, dopamine, glutathione are just a few of the photoreceptors destroyed by ferroptosis. This is why photobiomodulation seems to help in some of these disorders, in my opinion. It helps reverse cell death from this mechanism. Few people are making these links in the literature.
The classical view of cell death has long assumed that, once initiated, the dying process is irreversible. However, recent studies reveal that recovery of dying cells can actually occur, even after initiation of a cell suicide process called apoptosis. This discovery raised fundamental key questions about which forms of the cell death process could be reversible and how reversal is mediated. Recent study results reveal the first evidence that ferroptosis is reversible and they have suggested strategies to enhance its reversibility. We are now using those ideas in helping our clients out at Kruse Longevity Center. bio.biologists.org/content/8/6/bi…
Read 5 tweets
Aug 16
1. Today's lesson: Your longevity experts are RETARDS.
If you know you know. This is the lady below that shows you every longevity expert out there is FOS. She is and was the ultimate wellness rule breaker who lived 122 years and 164 days. Longer than anyone in recorded history.Image
2. Her daily routine:

↳ Smoked 2 cigarettes daily until age 117
↳ Ate 2 pounds of chocolate per week
↳ Drank Port wine regularly
↳ Doused everything from the Sea/land in animal fats and olive oil

She also took up fencing at 85. Rode her bike until 100. Walked until she was 110. She only quit smoking because she went blind and could not see her cigarette to light it. She was the opposite of this rich moron below.Image
3. The Decnetralized Science Behind It

Her mitochondrial colony were exceptional. She sat out in her flower garden every day of her life. She was a young woman when the Eiffel Tower opened and was present. She was there for its 100th anniversary as a guest of the French government. Studies on her found she had mitochondrial epeigenetic variants that enhanced cellular photo repair and maintenance.

She was the first human who showed us that environment trumped our nDNA and diet. But centralized science continues to miss this lesson and you pay that toll every day with their evidence based advice.

None of you realize it. How can I say this?

Did you know that recently a paper was published in Nature Medicine that was a massive analysis from the UK Biobank on this topic. Do you know what it revealed? It revealed the lesson Ms. Calment life; that our environment – the "exposome" of everything from air pollution to workplace light stress packs a bigger punch on how you age and die than your diet or DNA ever could. It tells us why all our longevity advice is horribly flawed.Image
Read 12 tweets
Aug 7
1. This interaction is governed by the Chiral-Induced Spin Selectivity (CISSS) effect, where spin-polarized photons or electrons preferentially match the protein's chirality. In photosynthesis, this spin selectivity may guide exciton transport through protein complexes. If a biophoton's spin aligns with the protein's symmetry, it can trigger excitation or release; otherwise, the signal may be lost, suggesting spin could be nature's way of encoding selective bio-communication.
2. Mitochondria convert food into electrons via the electron transport chain, where cytochromes (especially cytochrome c oxidase) pump protons out, reducing oxygen to water. Proton tunneling, not just bulk diffusion, enables this rapid proton movement (over 10³ protons per second). ATP production peaks during awake hours and initially rises during sleep onset due to free fatty acid (FFA) release, but drops sharply in REM sleep to support a quantum state for brain recycling.

During uncoupling in deeper sleep, mitochondria release infrared heat, condensing surrounding water and coupling to quantum processes.

This mirrors spintronics, where electron spin, manipulated by electric and magnetic fields, stores information, much like mitochondria control electron spin for energy and life processes. Free radicals, with unpaired electrons spinning in the same direction, play a key role, defying the singlet state (paired spins) governed by the Pauli exclusion principle. This quantum spin manipulation underscores mitochondria's unique bioenergetic role.
3. When electrons with the same spin are excited by electric or magnetic fields, they enhance quantum processes in chloroplasts and mitochondria, which use Fe-S redox complexes as electromagnetic compasses to gauge environmental needs. These organelles act as quantum heat pumps, generating infrared light modulated by free radical signals to drive energy and signaling via the MINOS water layer. Water, with its high dielectric constant, breaks symmetry by separating charges and shrinks when heated by infrared, imprinting environmental signals as an ionic plasma. Its hydrogen bonding network acts as a quantum measuring device, recording the state of entangled electron pairs in free radicals. Mitochondria release monochromatic infrared light to entangle electrons and protons, akin to the double-slit experiment, while skin filters sunlight (optimal at 270 nm UV) before mitochondrial processing, reflecting a quantum-coupled design in evolution.
Read 24 tweets
Aug 7
Why dentistry needs to be decentralized badly: instagram.com/reel/DNDlNR1Ok…
2. Decentralized Answer:
My thesis leverages first principles in your question to me about LPR because light as energy, POMC as a UV switch, melanin as a charge modulator all link to propose that sunglasses disrupt UV-driven biology, reducing melanin and charge, and potentially causing LPR via glycation and neural crest effects. The UV-POMC-melanin link is solid; the LPR and charge extensions are cutting-edge hypotheses needing research.Sunglasses,

UV Light, and Melanin Production: Principle: Light is electromagnetic radiation, and UV photons (e.g., 280–315 nm UVB) carry energy that excites molecular chromophores in skin cells, triggering biochemical cascades. POMC (proopiomelanocortin) expression is a photochemical process driven by UV light, as confirmed by studies (e.g., Slominski et al., 2018) showing UV-induced upregulation in keratinocytes and melanocytes.

Mechanism: UV photons activate POMC transcription, leading to α-MSH production via the melanocortin 1 receptor (MC1R) pathway. α-MSH stimulates melanogenesis, producing melanin, which absorbs and dissipates UV energy, protecting tissues. Sunglasses Effect: Sunglasses with UV400 protection block 100% of UVA/UVB. If UV is the sole trigger for POMC translation, blocking this spectrum halts the signal. This reduces α-MSH and melanin synthesis. The extent depends on exposure time, but chronic use could significantly lower baseline levels, especially in low-pigment individuals. The claim holds, sunglasses directly reduce melanin by cutting the UV-POMC- α-MSH pathway.
3. Ciliary Ganglion and POMC Disruption: Principle: The ciliary ganglion regulates pupil size and lens accommodation via parasympathetic innervation (95% of its neurons target the ciliary muscle). Light spectra influence autonomic signaling, and neural crest cells (originating from POMC-expressing regions) migrate to form pharyngeal and laryngeal structures. Mechanism: UV light, absorbed by retinal and skin chromophores, modulates POMC processing into its 10 peptides (e.g., α-MSH, ACTH). Sunglasses alter the light spectrum reaching the eye, potentially mimicking non-native electromagnetic fields (nnEMF) by shifting the input from natural UV/IR to artificial blue light. This disrupts POMC translation, affecting neural crest-derived tissues, including the pharyngeal pouches. Sunglasses mimic a ciliary ganglionectomy (surgical removal). Sunglasses functionally alter light input, which indirectly influences ganglion-mediated responses and POMC signaling. The nnEMF mimicry is plausible because blue light (400–500 nm) from screens differs from UV (280–400 nm) in energy and penetration, potentially misaligning cellular clocks and POMC processing.Image
Read 8 tweets
Jul 30
While the tweet is correct, my tribe knows Dr. B is someone's advice to avoid. He has no idea about the quantum biology of NO. His advice was so bad I had to cancel a member's membership over this.
2. NO to excess is a danger. I saw this first hand in New Orleans during HIV. Image
3. UV sunlight stimulates vitamin B12 synthesis, red blood cell production, NO release (lowering blood pressure, increasing venous oxygen), and stem cell activity, with corrin-bound NO modulating its bioactivity as a GOE legacy against oxygen toxicity.

The Coulomb force (∇·E = ρ/ε₀) amplifies skin’s electrostatic fields, optimizing these processes, with potential significance in Nodes of Ranvier (nerve conduction) and retinal vasculature (blood flow).

In California for example, nnEMF, smog, and lifestyle factors disrupt this photobiology, reducing 25(OH)D, B12, and NO, driving many diseases like atopy, eczema and autism (1 in 24 children, 2025). Maternal disruptions in this system induce many epigenetic changes, amplifying transgenerational risks versus Florida. ICD-10 code use in California W90.0 supports nnEMF’s role in how excess NO can harm.Image
Read 11 tweets

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