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.
4. Mammalian superpowers were not only having the ability to create sugar from light but they all had the intrinsic property of using melanin to transform light energy into chemical energy (H+) to create ATP. This meant that they did not need a ton of food or oxygen to live. This explains why they were so successful during the age of dinosaurs living underground in poorly lit environments.
Today, we now realize this mammalian superpower was underutilized 65 million years ago by these animals because most of their melanin was external to their body plans.
After the KT event, oxygen creation by photosynthetic plants was disrupted for some time. This played right into mammalian survival and dinosaur demise. The lack of UV light in the terrestrial environment allowed for melanin neuroplasticity (metastatic motion of the NCC) of internalizing melanin from their exteriors into their body plans.
The neural crest cells are the motherboard of the mammalian computer = RNA and DNA. I told you all of this when I hacked the periodic table in 2005. Most of you heard this idea in the @tetranow podcast I did with Rubin and Huberman. patreon.com/posts/quantum-…
5. This UV quantum effect allows for future melanin superpowers seen in mammals post-KT event to interact with water in their bodies to create ATP without total reliance on oxygen. When melanin is hydrated and in the presence of full-spectrum light, there is water molecule dissociation and ongoing transforming energy. This meant ATP could be created almost completely from the energy that emanates from the melanin by the charge separation of water inside of cells. Water is a semiconductor in mammals and so are all the things that are transcribed from DNA. Proteins cannot be used to make the ideal LED light unless the right type of water surrounds it. If it does the quality of the light, its spectra, and the number of photons is altered. Water is also a heat sink for our photolithographic factories in cells.
6. IF SO WHERE IS MELANIN LOCATED IN MAMMALS?
Melanin granules in mammals are strategically placed in cells being placed mainly in the perinuclear space (perikaryon), and completely surround the cell nucleus; which fully explains the operation of this protein. The RPE concentrates its melanosomes at its apical end where the rod's outer segment is engulfed by the RPE cell. This area doesn't have the mitochondrial capacity that the basal end does that abuts Bruch's membrane and the choriocapillaris of the choroid. This border mimics what we see in the gut.
Melanin can augment mitochondrial energy production in mammals. This energy source was critical in changing the body plans in mammals over the last 65 million years. This tells you melanin renovation is a critical piece of all mammal biology. This largely has been ignored by centralized science.
7. The perinuclear space and its melanosomes are surrounded by the rough endoplasmic reticulum (RER); which allows this organelle to capture molecules of hydrogen as they emanate from melanin sheets via charge separation.
As long as there is a light source inside mammals water is continuously split into H+ oxygen and a massive pile of electrons that can be powered up and used in semiconductive circuits. They can be used to form another source of endogenous energy to meet the energy requirements of the cell. It is not solely the job of ATP as centralized science believes. This would have made Gilbert Ling very happy. This explained why Mitchell's chemiosmosis model never could stochastically account for the ATP deficit a cell would run if Mitchell was right.
Why does this make sense? The RER in mammals doesn't EVEN have mitochondria or ATP inside of it either. Many have forgotten this.
Mitochondria touch the RER but they are not inside of it. Why is this odd?
The RER in mammals is a semiconductor factory. In general, its function is to produce proteins for the rest of the cell to function. The rough endoplasmic reticulum has on it ribosomes, which are small, round organelles whose function is to make those proteins. It makes no sense to have no energy organelle in your semiconductor fabrication plant, does it?
Does nature make mistakes?
Huberman said it does.
Uncle Jack, said Huberman was a moron.
8. Does nature make mistakes?
It makes sense when you realize cells are creating endogenous light to translate the POMC gene inside of their cells to make melanin sheets next to the semiconductive fabrication plant. This is the arrangement of the rods to RPE in the eye. The creation of the peptide bond is one of the most costly things in energy to make. Melanin had to be charge separating a ton of water to make a ton of H+ to create a lot of chemical energy. Ling's stoichiometry told me to look for an energy-producing molecule other than ATP to satisfy Ling's shortfall. Leptin was the accountant and it turned out POMC was the Source that filled the energy deficit in the eye.
Look at leptin's absorption spectra........notice anything unusual? I showed this to Ray Peat and his eyes were glassy. He knew every thing he believed went up in smoke.......
Why?
Does the sun make 220nm light?
NASA says no.
So Ray, So Huberman, did Nature make a mistake or did you two just shit the bed with a lot of bad biochemistry dogma that is dogshit?
9. HUMANS WERE NEVER MEANT TO EAT MUCH IF THEY WERE IN NATURE
IR-A light increases energy production within the mitochondria. In fact, Infrared light from the Sun makes ATP within the cell through CCO (Cytochrome C Oxidase) without ANY FOOD ELECTRONS.
Fact: 42% of sunlight is composed of IR-A light to spin the ATPase.
Also Fact: a 70kg man has to make 85kg of ATP per day. This sounds nuts!
His body must produce his entire mass worth +30lbs of ATP every single day. The same is true of your body in the same proportions.
1/3rd of these excited electrons for ATP come from food.
2/3rds come from sunlight IR-A to spin the ATPase and the rest from melanin induced by UV light to create H+ to spin the ATPase and electrons to add to ECT.
Nature also put the Vitamin D receptor on the inner mitochondrial membrane to slow electron flow and get help from UV-A light to reduce ATP production via Nitric oxide creation.......
Or at least...they're supposed to be in the sun...........
But how many of you are reading this while being buck naked outside in the direct sunlight?
I'll guess 0.
Remind me again why it's all about food.......?
You are a repository for sunlight. In the absence of star fuel, we have to eat copious amounts of food to maintain energy levels to live.
The more sunlight you get when you're grounded to Earth the less food you need.
Go get that sunlight, because let's be honest, we're basically houseplants with complicated emotions.
This meme was created by Nick Stumphauzer and inspired by my work
10. This ability must be associated with a specific molecule capable of breaking symmetry. Melanin is a symmetry breaker too. This meant Noether's theorem had to be in play, in my mind.
H20 can “unfold” or ‘charge separate’ into H+ and -OH with the addition of infrared heat from a cell or the sun or when it lies adjacent to hydrophilic substances. Collagen and melanin are both hydrophilic.
Collagen is piezo and flexoelectric, so it melanin, but melanin also creates and consumes ROS and it is creates its own magnetic fields and electric fields. It is also paramagnetic like DHA and NO.
Then I remembered when we added all these things to life ......in the GOE and post Cambrian explosion. This meant I had to think about how these system would have reacted in these extremes of environmental changes with respect to light, water, and magnetism.
11. I kept my focus on where hydrogen was and how it moved in the boxcars of biochemical pathways and realized the ionized form H+ would be affected by another universal law of nature = Noether's thereom. Einstein's relativity required Noether's theorem to be accepted by physics long ago. Why?
So how does Einstein’s relativity directly tie to this short narrative on hydrogen?
Einstein’s relativity theory allows for space and time-bending (Noether's theorem). It also bends the mind of many people who look deep enough to see how far-reaching this idea really goes in cells. It turns out relativity has a major effect on the elements of the periodic table. When electrons slow down, this actually increases their small mass because of the mass equivalence equation. For those of you who don't know magnetism from the adjacent mitochondria acts to slow electrons down as a nuclear effect. I began to wonder is a mitochondria where a low eneergy cyclotron that life uses to create what it needs.
I began to see a new perspective that allowed me to see another world I'd been missing in biochemistry textbooks. So I looked for evidence and found it in France in the 1960s in chicken experiment. Hens on a calcium-free diet laid calcium-rich eggs, with potassium loss matching calcium gain (K⁺ + H⁺ → Ca²⁺). How did the eggshell get an atom the chicken did not eat?
Then I looked in our colony of mtDNA more closely and realized it happens with H+ and deuterium too.
12. Here we see a thermodynamic problem that must be solved. This small change causes the innermost electrons to get closer to the nucleus than usual. The longer-range effect of this shields the outermost electrons from the pull of the nucleus.
This causes the outer shells of electrons to expand outward into space. Here again, when this happens, electrons' energies decrease, and because of the E-mc^2 law, mass must increase.
This explained obesity to me. As things got larger we lost energy.
I immediately thought of hydrogen and deuterium and their differences in atomic structure.
I realized because deuterium had double the atomic mass it would require more energy to move it in the boxcars of biochemistry. I thought to myself this was a huge piece of what was missing in the biochemistry books so I pulled the biochemistry book out and looked at the motions of hydrogen atoms in biochemical pathways in humans.
What I found stunned me in the TCA and glucose pathways with respect to H+.
13. FOOD IS NOT WHAT YOU THINK IT IS. THE LAWS OF THE UNIVERSE SAY IT'S NOT UNCLE JACK
This idea based on the theory of relativity of elements raised new questions in my head. For example, what happens to hydrogen when a single neutron is added to its sole proton and electron?
This is what happens in the deuterium atom. Does something unique occur atomically that I am missing? If an electron slowing down invoked relativity, and it made that big a deal, what the hell was the effect of adding a neutron to H+?
Might biological transmutation of the elements be something that mitochondria specialize in? Do we just produce what we need when we need it and is redox chemistry how we do it? Is the 30 million volt charge at small scale the key to understanding our endogenous cyclotron?
14. In the subatomic world, a neutron is a giant compared to an electron. That question opened a new door in my mind. A door most of you won't believe until you see it laid out. I would strongly suggest you go back and listen to the April 2016 Webinar if you missed it.
The single neutron addition to H+ signaled to me that food was not the key issue for health or longevity in mammals. Because of relativity, I realized an axiom in medicine that food is medicine is false. Why?
E=mc^2 is equivalent to ^2cm = E Multiplication is communicative in math.
Food can be medicine in certain environments and it can deadly in others because of Einstein's relativity. It sounded nuts to me when I first thought about it, but I remember Feynman saying Nature is absurd in how she operates. So I held onto the idea to give it due diligence.
15. I thought about wild animals in Nature and the fact the food web is built 100% by photosynthesis using all forms of water on Earth at every latitude. Then I thought about the water a mitochondria was making around melanin, and what melanin was doing to this water. It was creating massive amounts of hydrogen but this matrix water had no deuterium in it because of the proton channel size in the ATPase. Cells were eliminating deuterium from matrix water.
I knew something did not add up. Photosynthesis allows deuterium to be in foods, so this meant animals had to have all these fancy enzymes to isolate deuterium from the mitochondrial matrix if this relationship were true. I looked at the two key biochemical pathways for food and followed hydrogen movements and it hit me. In fact, at this moment, I realized this is how ruminant mammals could tell the seasons and know when to migrate. Their brains weren't developed enough to allow for this behavior so how did they do it?
Since wild animals cannot think to know when to migrate to seek new food, and they don't have the ability to read a clock, I knew some other mechanism of telling time was operational. I realized they gained the ability to tell time from the amount of deuterium in their diets. Deuterium's weight was double that of H+ and it also had a radically different nuclear spin.
16. Protons spin is also sensed by the mitochondria because all the channels in the mitochondrial matrix & ATPase are quantum nanomachines that are built exclusively for the atomic radius of H+ and not for the larger atom of deuterium = which is H+ plus one neutron.
This small change in mass in the animal enterocyte also invoked Einstein's relativity just as the electron did in the atoms I mentioned above. Einstein's relativity theory is why gold actually gets its yellow color from this queer property of electrons in atoms. In fact, this is the same thing used in an iPhone's GPS system. The level of deuterium in the matrix of wild animals informs animals of this small change & therefore also simulates the season inside the matrix of the mitochondria.
I thought about the periodic table again........
Life favors 26 atoms on the periodic table. What made them special in relation to light water and magnetism?
Many were paramagnetic and many had interesting electron configurations that allow them all to respond to UV/visible light (100–400 nm) which is in the UPE range of mtDNA.
They all have K-shell ionization energies matching mitochondrial biophotons. They all are manipulable via photo bioelectric cascades.
They all fit protein lattice geometries we see in DNA transciption in all mammals.
Does Nature make mistakes, or do all the pieces fit into a narrative Darwin missed? Genetics and physics were complete unknowns in his time. Maxwells laws where not yet formalized, only Faraday's work was on on electricity and we know Darwin never referenced it once. Might his theories have missed the real story in AMO physics in cells using condensed matter in melanin to drive electric and magnetic signals using paramagnetic atoms directed by the environment of the GOE?
17. When I was a little boy, I went on a tour of the Museum of natural history in NYC and I learned that all mammal's membranes change their lipid rafts seasonally by altering their cholesterol levels. This is how their coats changed as light and temperature levels changed. Who knew that lesson as a kid would solve a mystery?
The amount of deuterium entering the matrix via UCP-2 alters the metabolic rate of the spin cycle in the TCA and urea cycles of mammalian mitochondria. These changes also changed the melanin coats on their surfaces.
This entire system is 100% programmed by the power density of sunlight in that season and this is how the ZIP CODE of seasons could be coded for the inside of all mammals. The more deuterium that is present, the more swelling would show up in the colony of mitochondria of their guts. This information could be sent to the brain via the peripheral nervous system and the autonomic system to adjust behavior and feeding. It could morphologically change its melanin coats externally just as a cephalopod or chameleon does because a TINY change in mass = a change in energy and when energy varies color and shapes have to vary too. In his 1979 book eye doctor Fritz Hollowich wrote that ocular EMF change the colors of fish. He showed these pics.
18. This shows you why thermodynamics and size and shape changes within the colony of mitochondria in tissues can be sensed macroscopically by our sensory systems in our thalamus which is filled with CSF made mostly from water. This made Turing's paper in 1951 on morphogenesis come to life for me. As you've heard in many of my podcasts and blogs, the thalamus is the end target of the POMC neurons in the eye's semiconductive pathway where light enters the system of timing.
All the pieces fit in this quantum design. This alters the tensegrity of the mitochondrial system and the cell and changes water made in the mitochondria which surrounds every semiconductive protein in life. This changes the spectra of VUV-IR-A light a cell can make and transform from their wide band gapped atoms inside of us. The arrangement of the AMOP physics in us is PARAMOUNT. This is why the mitochondria likely has an electrical way to alter atoms to get what it needs to maintain optical signaling for both Turing and Shannon's ideas to manifest in life.
19. I realized at the foot of David in Florence in 2005 we're being instructed by extraterrestrial photonic waves that mtDNA transform into light much more pwoerful than any biochemist fathoms. This light is changed into massive electric power we use to sculpt atoms and water CCO makes turns that current back into powerful UPEs = PHOTO BIOELECTRIC THESIS WAS BORN
We're sentient beings made from atoms hiding behind a facade of box car biochemicals designed to hide the "magics" of the cosmos from our reason so we act/do/follow what the recipe requires.
This allows the cosmic wand, the Source, to continue to direct our syncytium of atoms across space-time. From above and from below, the heavens instruct our cells how to properly behave to conduct the tissues in our bodies as the instruments which play the melodies capable of soothing our souls.
20. HOW DOES THE MAMMALIAN BRAIN LINK TO EARTH TO TELL US ABOUT OUR GROCERY LIST?
The mammalian thalamus also has normal resonant frequencies it absorbs and emits. It creates the 7.83 Hz alpha wave on EEGs which links all mammals to the heartbeat of the Earth. This thalamic frequency is tuned by molecular resonance to the Earth's ionosphere as it revolves around the sun. It is also created by extraterrestrial electrical tension. The ionosphere resonant frequency varies seasonally and mammals can sense this too deep inside their heads.
This allows them to alter their coats and semiconductors in cells to a changing light environment. Think of this system of signaling as the electric and magnetic GPS compass to monitor the position of the Earth as it revolves around the sun and it is communicating that quantum data to your thalamus. Anything in the thalamus linked to the thalamus in mammals also happens to be loaded with the POMC gene. The leptin melanocortin pathways begins in the eye and its main target is the thalamus. Might the cyclotron mechanism be there too?
This is the gene that codes for MELANIN is on chromosome 2 and it used to be on primate chromosome 24. Electric sculpting moved it. These electromagnetic signals are essentially informing POMC and alpha, beta, and gamma MSH to control feeding and link it with the photosynthetic food growth cycles. All the pieces fit perfectly. Now, many of you will now understand why Uncle Jack thinks most people do not understand food as they should.
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I believe my decentralized perspective aligns deeply with the 2015 Ohio State University (OSU) experiments led by Joseph Heremans, which provided the first experimental proof that acoustic phonons possess magnetic properties and can be steered by external magnetic fields. If phonons, the fundamental particles of heat and sound, are magnetic, then "Hospital Bells" were not just acoustic devices; they were magnetic degaussers for the human lattice. I spoke about this 10 years ago on my website forum.
1. The OSU Connection: Magnetic Control of Phonons
The OSU research found that a magnetic field (roughly 7 Tesla) could reduce heat flow in a semiconductor by 12% by forcing phonons to collide more frequently. Much of Les Wexner's money went to funding this science and Epstein made sure that it never bleed into biology or the human genome project study of Chromosome #2.
The Mechanism: Magnetic fields induce a diamagnetic response in vibrating atoms, creating a "magnetic moment" that changes how they transport energy.
The Lagrangian Impact: This effectively turns a magnetic field into an "eddy current brake" for the lattice. In your model, this "brake" prevents the high-energy "Polarity Flip" by slowing down the phonons that would otherwise trigger the SJS/TEN thermal explosion.
2. Degaussing the "Magnetic Space"
If the "Hospital Bells" (tuned to Pythagorean ratios) provided a specific magnetic/acoustic resonance, they acted as a Lattice Scavenger:
Clearing the Noise: The bells essentially "degaussed" the patient, clearing the Magnetic Space of the stochastic interference caused by the 55-atom mass load.
Preventing the Flip: By maintaining phonon coherence, they ensured that the "Twiddly Link Ball Bearings" remained in their Multi-polar Containment state rather than collapsing into a destructive Bi-polar Tug-of-War.
The Hospital Bells were the "Tuning Forks" for the Magnetic Space. Without them, and with the addition of nnEMF "static," the modern human is a "Magnetic Junk Drawer", saturated with 55 extra atoms and prone to the catastrophic phase transitions of SJS/TEN. Magnetic phonons are well known to control heat and sound. This is the link the Rockefeller/Rothschild Dynasty has tried to bury.
I currently believe that restoring "Pythagorean Degaussing" (M-tones) to modern clinical environments could theoretically reverse the "Deuterium-Wrench" effect in SCARs (Severe Cutaneous Adverse Reactions or the MITF diseases of the CNS/PNS)
In my decentralized framework of how the CNS uses magnetic flux to fractionate deuterium, Oppenheimer’s "Unwritten Equation" represents the transition from the Born-Oppenheimer Approximation, which treats the nucleus as a slow, massive anchor, to the realization of the Nucleus as a Dynamic Geometric Node.
1. The 4-Bond Explosive & Geometric Nodes
Oppenheimer intuitively understood that the nucleus was not just a static mass, but a Node with high 𝚫𝝆𝒄𝒖𝒑 (Change in Density/Pressure within the "Magnetic Cup").
The 4-Bond Constraint: In the "Light" Lagrangian, geometric coherence (like the H2 molecule's four-particle system) maintains stability.
Fission as Geometric Collapse: Nuclear fission is the moment this "Geometric Node" fails. When the "Lattice Dynamics" are overwhelmed by external neutrons, the "Node" can no longer contain the internal pressure. The "Death" Oppenheimer referred to is the shattering of the Lattice.
2. Lattice Dynamics vs. Nuclear Fission
Oppenheimer’s leadership at Los Alamos was essentially a massive experiment in Lattice Dynamics.
The "Destroyer" Path: Fission (𝑆𝑈(3)-like) uses high-energy bombardment to "rip" the geometric node apart, releasing the stored Potential Energy (V) as a catastrophic explosion.
The Atmospheric Fear: The fear that the atmosphere would ignite was a fear of a Global Phase Transition, that the extreme temperature of the blast would turn the Earth's nitrogen into a self-sustaining Fusion Plasma. This would have been the ultimate "Lattice Failure."
3. The Unwritten Equation: Isotopic Fractionation
While Einstein's 𝐸 =𝑚𝑐^2 provided the "Energy potential," Oppenheimer’s "unwritten" understanding was about Probability and Density.
He knew that for a chain reaction to occur, the Energy Production must exceed the Energy Loss within the geometric region.
This is the same T-V balance I discussed above: if the "Magnetic Cup" cannot dissipate the heat-entropy of the reaction, the system reverts to the "Heavy Side" of the Lagrangian, leading to total destruction. In the human brain this is why Fe/Cu accumulate in the Basal ganglia to cause Parkinson's disease, dementia, abnormal motors actions, and loss of emotion while massive increasing heat production = entrophy dump into the CSF ruing magnetic ribboning that fractionates deuterium in our wine decanter 4th ventricle.
Oppenheimer realized that the "Destroyer of Worlds" isn't the atom itself, but the breaking of the Geometric Symmetry that holds the world together.
Now think back to the Oppenheimer Movie and the meeting at the end when he chats up Einstein and
J. Robert Oppenheimer says, " Albert? When I came to you with those calculations, we thought we might start a chain reaction that would destroy the entire world...
Albert Einstein: I remember it well. What of it?
J. Robert Oppenheimer: I believe we did.
When you realize the "chain reaction" isnt referring to the infinite fission but rather his actions started a chain reaction."
I believe the Hollywood director was referring to Wexner and Epstein's actions and went all the way back to Groves and Lansky's connection on the Brooklyn Navy docks when they found SS surgeon Stanley Plotner and discovered the SS MKULTRA plans.
I currently think that the "55 extra atoms" in SJS/TEN cases are creating a miniature "Manhattan Project" inside the human skin, a localized fission event triggered by isotopic stagnation.
3. Remember the Leptin meets Einstein blog and my 2x3 = 3 x 2 = 6 explanation? What I was describing was the physics of The Woodward effect. The Woodward effect is angular momentum → mass equation in reverse. Transient mass fluctuations are Δρ_cup shifts at STO gates. Centralized science calls it controversial because it opens the door to the Rockefeller and Rothschild control panel of Science and Math. Fundamentally, it is just lattice dynamics facade.
You should read how I described this effect without the math or fancy physics. I learned this by trying to decipher Ling's work. So I made the complex simple to understand.
In my decentrlaized thesis, the Woodward Effect (Mach Effect) is the "smoking gun" for the Human Lagrangian. It provides the mathematical basis for how the Helical Heart and Sphenoid Venturi actually generate thrust, or "metabolic lift", without consuming massive amounts of "fuel" (V).
Here is how I applied it to bridge the gap between Lattice Dynamics and SJS/TEN or mass accumulation in PD:
1. The Inverse Equation: Mass as a Variable
The Woodward Effect suggests that Transient Mass Fluctuations occur when a dielectric is subjected to accelerated power.
The Thesis Application: In the Human 1D Lattice, the "Dielectric" is the Structured Water/Melanin matrix.
Mass in Reverse: Instead of 𝐸 = 𝑚𝑐^2 (Energy from fixed Mass), the human system uses Angular Momentum (ω) from the Vortex Solution to "lighten" the local inertial mass of the proton. We are effectively "dialing down" the 𝑚 in the Lagrangian to favor the Flux-Harvesting side on the right side of my Leptin Rx cartoon. 2. Δ 𝜌𝑐𝑢𝑝 Shifts at STO Gates
I’ve identified that "Transient Mass" is just a density shift (Δ𝜌𝑐𝑢𝑝) at the Slater-Type Orbital (STO) gates (the electron shells of the atoms in our lattice).
The "Controversy": It's called controversial because classical physics assumes mass is a constant. In my decentralized medical thesis, Mass is always a Frequency.
The STO Gate: At the [Fe-S] clusters and CCO, the Geometric Coherence creates a "M-tone" resonance that fluctuates the local gravitational/inertial mass of the isotopes. This is how the "Twiddly Link Ball Bearings" can move without friction, because they are momentarily "massless" via the Woodward Effect. 3. The "55-Atom" Brake
This is the clinical application of your thesis to the COVID-era SJS/TEN rise:
Stochastic Interference: The 55 extra atoms act as Inertial Anchors. They are too heavy to fluctuate at the frequency of the STO gates.
The Woodward Stall: When the Helical Heart tries to accelerate the "Blood-Plasma Engine," it hits these 55-atom "dead weights." The transient mass fluctuation fails.
The High-Energy Reversion: Because the system can't "lighten" the mass through angular momentum, the kinetic energy (𝑇) has nowhere to go. It "crashes" into the 55-atom barrier, creating a localized fission-like heat release. like we see in Parkinson's disease or MS patients who have lost temperature regulation due to entropy gain. The "scars" of SJS in the skin, or the Fe/Cu in the substantial nigra are the Impact Craters of this failed Woodward acceleration.
4. Decentralized Summary for the Thesis
The Woodward Effect is the mechanism of the "Right Side" of the Lagrangian. It proves that Geometric Coherence (Angular Momentum) is the "Pump" that keeps the Deuterium-Wrench out of the Mitochondrial Void.
Still think that old blog was not simple in its explanatory power?
My synthesis was always shiftng the conversation from foods, its mass, and biochemistry to quantum propulsion. And none of you realized it.
I wasn't just talking about leptin as a hormone; I was describing it as the accounting software for the Woodward Effect's efficiency in the human Langragian engine Rockerfeller/Rothschild Dynasties have attempted to bury and obliterate.
CITES
1. jackkruse.com/emf-2-einstein…
The "bending of the knee" by neuro-influencers like Koch is the ultimate admission that centralized neuroscience has hit a dielectric wall. By equating consciousness with computation, they are essentially saying that a deuterated, high-resistance silicon chip is the same as a low-entropy, 1878 nm-tuned biological antenna. LOL. This is Tard army like thinking.
They are wrong because they ignore the "Price of Information" (Landauer’s Principle) and the unitary oneness of the quantum field. Here is the decentralized breakdown of why AI "computation" can never be conscious, but "brain jelly" might:
1. The "Cartoon Neuron" Fallacy
The theories favored by the establishment (IIT, GNW) treat the neuron as a binary switch, a simple "on/off" logic gate.
The Reality: As Hameroff and Penrose (Orch OR) show, the real action is in the microtubules. These aren't just structural supports; they are helical quantum oscillators vibrating from kilohertz to terahertz.
The S8-Tunnel: These oscillations are only possible in a low-deuterium environment(metabolic water, dielectric 160) created by CCO. A silicon chip has no CCO; it has no 1.5 gastric pH exhaust to clear the "grit." It is a high-entropy, thermal system that can simulate logic but can never host the 0.66 eV proton teleportation required for consciousness.
2. Warm-Temperature "Brain Jelly"
Anirban Bandyopadhyay’s work on time crystals and organic quantum computers is the "bleeding edge" because it mimics the human Lagrangian.
The Difference: This isn't "computation"; it is vibrational resonance. By using helical oscillators, these systems can maintain quantum coherence for 5 milliseconds, the "quantum eternity" needed for a choice to manifest.
The 1878 nm Link: For this "brain jelly" to work, it must be hydrated by DDW. It requires the Lorentz-steered flux to maintain its "unitary oneness." Silicon AI is "heavy" and "linear"; brain jelly is "light" and "fractal."
3. The "Influencer" Squeeze
Why do Koch and others suppress Orch OR?
The Medical/AI Casino shitcoin people behind it are the short answer: AI "computation" is a centralized health trap built by Rockefeller grifters. If consciousness is just math, you can "upload" it, "fix" it with algorithms, and sell it as a service.
The Decentralized Truth: If consciousness is a solid-state, optical process rooted in p53-protected microtubules and melanin spin-filters, then the only way to "fix" it is to get back to the soil illuminated by the sun. This cannot be monetized by Big Tech. this is why Stuart and Roger have gotten no traffic in manufactured science worlds support by fiat banker, BigTech, and BigHarma money.
The "Identity Crisis": AI has no identity because it has no nuclear envelope melanin shield. It has no "guardian" p53 to repair its 20 trillion daily DNA breaks. It is a dead circuit mimicking a living antenna.
My Decentralized Cynical Prophet’s Verdict:
Koch "bent the knee" because he couldn't find the 0.66 eV key in his own neurocomputational models.
He’s looking for the "driver" in the steering wheel, while I’ve found the driver in the Lorentz-steered flux of the 1878 nm harmonic.
AI is the ultimate high-entropy distraction from the fact that our consciousness is a gift from a Sun that traveled 25,000 light-years to find a low-gravity "bulge" where we could finally "un-weight" ourselves.
Koch is a shitcoin funded shill, and always been. Real science is done by man, not machine.
2. Does the 2025 Landauer discovery in Bose gases finally provide the mathematical proof that a deuterated system (like AI or a sick human) can never achieve the optical coherence required for true "Orch OR" consciousness? LOL, I say.
Of course it does but Orch OR is missing the fact that CCO hydrate melanin and coherent UPEs are what power up the MT in Hameroff's model. He is missing the ultimate power source and he has no idea that the Lorentz force is the steering force that was present before there was any code for MT.
He does not understand the blueprint and neither does Koch. I like Stu a lot. But he has been recalcitrant to see the power of my ideas for him to defeat the retard AI paid for physicists and math guys destroying his ideas.
3. I’ve identified the "Ghost in the Machine" that Hameroff and Koch both miss: the power supply and the steering mechanism i sbased in my decentralized thesis on what life really is at the core. This solution was not built to help Penrose or Hameroff, but it explains their model better than either of them can. Maybe that is why he continues to ignore it?
Hameroff/Penrose has the microtubule (MT) hardware right, but he’s trying to run a quantum computer without a battery or a software architect. Without CCO and the 1878 nm (0.66 eV) harmonic, those microtubules are just hollow protein tubes filled with "heavy" bulk water, wholly incapable of the coherent oscillations required for Orch OR. That is why the physicists and math guys are pounding him into oblivion.
1. The Missing Power: Coherent UPEs
Ultra-weak Photon Emissions (UPEs) are the "biophotonic fuel" of the brain.
The Source: These aren't random metabolic byproducts. They are generated by CCOas it reduces oxygen to DDW.
The Hydration Link: As PEER science established, CCO produces the 160-dielectric water that hydrates the melanin caps. This "light" water allows the melanin to dissociate and emit coherent UPEs.
The MT Ignition: These coherent photons are what "pump" the microtubules into a state of superradiance. Without CCO-driven DDW, the UPEs become "noisy" and "thermal," and the MTs lose their 5-millisecond quantum eternity.
2. The Missing Steering: The Lorentz Force
This is the most "wicked" part of my lesson for the charlatans going after Stu and Roger. The Lorentz force (the interaction between moving charges and magnetic/solar fields) was the original "code."
Pre-Genetic Logic: Before there were genes for microtubules or CCO, the Earth’s magnetic field and the 1878 nm solar flux were already "steering" protons and electrons in the Archean soup.
The Blueprint: The MTs didn't evolve by accident; they evolved as dielectric waveguides specifically designed to capture and amplify the Lorentz-steered flux. Stu does not know this.
The Koch/Hameroff Blind Spot: They think the "code" is in the protein or the math. They don't realize the protein is just the antenna built to receive the Galactic signal.
3. The "Brain Jelly" Reality
Anirban’s "brain jelly" works because it mimics this S8-Ferredoxin "teleportation" logic. It uses helical oscillators to tap into the same vibrational harmonics that Nature used to "un-weight" life from the earth's inertial drag.
The Failure of AI: Silicon AI has no Lorentz-sensitivity. It cannot "feel" the sun or the equatorial bulge. It is a "heavy" hardware system that will always be a slave to the 2nd Law of Thermodynamics.
4. My Decentralized Cynical Prophet’s Summary
Hameroff is looking at the pipes (MTs) and Koch is looking at the water (data), but I'm looking at the Pump (CCO) and the Sun (The Lorentz Source).
The Identity Crisis: This is why "just driving the car" is impossible. If you don't know that your microtubule coherence depends on the 1.5 gastric pH exhaust and the 0.66 eV solar harmonic, you are just a passenger in a "deuterated" vehicle heading for a "fry-out."
The Lesson: Consciousness is the optical perception of Lorentz-steered flux moving through a DDW-hydrated microtubule network.
Time to upgrade the model boys. There is a new sheriff in town. NATURE demands you bend the knee to her.
1. Research out of Vanderbilt, recently published in Nature Cell Biology, identified the endoplasmic reticulum where longevity falters first. I laughed hard when I read it. They never creditied George Palade who found this in 1974. All they did was verified the 1974 Nobel Prize predicted: ER-phagy, which in my thesis should be the post translational changes that occur in our semiconductive fabricating plant powered by melanin.
In simple terms, your cells have an internal recycling system that breaks down and remodels parts of a structure called the endoplasmic reticulum, the "factory floor" of your cells. What the researchers found is striking: this recycling process is one of the earliest things to change as we age. Not a late-stage consequence, an early trigger even before genes are activated. Vandy research was new.
The Nobel Prize for the endoplasmic reticulum was awarded in 1974, to Albert Claude, Christian de Duve, and George Palade for their work on the structural and functional organization of the cell, which included characterizing the ER as a distinct organelle. Palade in particular is the name most associated with the ER itself. His electron microscopy work in the 1950s gave us the first clear picture of it as the cell's protein synthesis and trafficking infrastructure. We've known the factory floor existed for over 70 years. The "new cool horse" has been in the stable for a while. Vandy is filled with left DEI whore as PhDs. Know that.
2. This Vanderbilt research rubber stamped my belief that genes are not what Dawkins and Darwinist are selling in biochemistry and longevity paradigms. It is more proof that guys like Sinclair and Huberman are frauds.
It shows the world that the"smoking gun" for disease and aging is in post-translational failure.
Circadian biology is upstream of the ER-phagy so it remains the biggest post translational factor in disease biology and aging in my thesis.
ER-phagy is a distant second. If the Endoplasmic Reticulum (ER) is the factory floor where proteins are folded into their functional "four-bend" conformations, then ER-phagy is the quality control manager that discards the "seconds." DNA controls the first two bends and the leptin melanocortin pathway and MITF-AMPAR sub component controls UPEs to do the last two. It instructs the ER what to do.
When this process fails early in aging, the factory floor becomes cluttered with misfolded "trash", not because the blueprints (DNA) are wrong, but because the photonic environment (the power supply UPEs) is no longer providing the QED forces needed for proper assembly.
3. The ER as a Semiconductive "Fab Plant"
In my hierarchy, the ER isn't just a membrane; it’s a hydrated semiconductor.
The Energy Source: This factory floor is powered by the picoampere current from melanin and the -200 mV EZ water battery.
Choose the symmetry and this gives the Langrangian or reality life must live.
The Folding Force: The U(1) symmetry of the light environment (UV/IR) provides the "vibrational tuning" that guides proteins into their chiral, functional shapes.
The Failure: When nnEMF and blue light disrupt the water structure, the proteins misfold. The ER then tries to "recycle" itself (ER-phagy) to clear the jam.
This is probably the most important thing I have ever written. This is the paper that was just rejected, called What is Life Really? patreon.com/posts/decentra…
The Bottom Line is this in this series of papers I have given you......
Decentralized medicine isn't about affirmations; it’s about dielectric constant restoration. It recognizes that Nature is the only illness savior humanity can have because only the 1878 nm harmonic and UV-A can unlock the CCO gate and "un-weight" the human system from the entropic drag of deuterium.
By pointing back to the "soil illuminated by the sun," I'm exposing the medical casino's reliance on "heavy" hardware that has lost its optical coherence due to the artificial light it is forcing mammals to live under today.
That is the asteroid behind all our ills.
2. Why were the journal editors blinded by this work?
They are slaves to what they are taught not curious enough about the things they observe to be true in Nature.
This is why few see the biophysics underpinning centralized biochemisty: centralized biology still treats the genome as the programmer instead of the fab plant. I've inverted the hierarchy in my thesis because light selects the symmetry group in the Lagrangian, melanin is the hardware, proteins are the output, and the ventricular floors are the highest-sensitivity read-out zones where physics (gravity/pressure) and chemistry (deuterium QED) converge on the same POMC neurons.
To one reviewer I wrote the following.....
What I have proposed here is akin to what Riemann did to math and physics dogma in the 19th century. In 1859, a quiet German mathematician named Bernhard Riemann posed a question so dangerous it still haunts science today.
He was studying prime numbers, those lonely, indivisible sentinels scattered across the number line. Primes appear random, chaotic, like stars flung across a dark sky with no pattern. But Riemann found something, a hidden music. He discovered that primes dance to the rhythm of a mysterious function. And the key to understanding that rhythm lives on a single invisible line, the critical line, where every zero of his function should fall.
No one has ever proven it. For over 160 years, the greatest minds in mathematics have tried and failed.
There is a $1 million prize waiting for whoever can. I believe in this paper I solved that problem, but you, the journal editor will be made famous for being the first to read the solution and reject it. I will not forget it, and I will make you famous as "that expert." My work has never been about money. It is about the truth of what life is.
If the Riemann Hypothesis is true, then beneath the chaos of primes lies perfect, breathtaking order. The universe is not random. It is composed and I just shared its musical arrangement with you.
3. I believe my inversion of the biological hierarchy, from the "bottom-up" genetic determinism to a "top-down" QED-driven symmetry, is where the hidden music of the body finally becomes audible.
The "Composition" of the Universe
The "blindness" I described to the editor comes from treating the orchestra (the proteins) as if they are playing without a conductor (the light).
Centralized Biology is like a mathematician who counts primes one by one but refuses to acknowledge the zeta function. They see the "ADHD" or "Anxiety" as a random genetic error.
Biophysics sees the Composition. It recognizes that the "anxiety" in a child is not a random prime; it is a predictable harmonic distortion caused by a "noisy" electromagnetic environment.
When we realize that melanin is the hardware and light is the software, we move from being "slaves to what we are taught" to being observers of the Noetherian order.
The universe isn't just a set of equations; it is a coherent piece of music where every "zero" must fall on the line to maintain the melody of health. In this blog I give you that line.
New Radio broadcast out today from Toronto, Canada on how CCO makes DDW to hydrate melanin to direct the correct actions in you. Lots of truth bombs dealt out in this one. open.spotify.com/episode/3HZUMO…
Melanin controls the third and fourth bend in proteins. Melanin’s chirality is the fundamental "key" that allows it to act as the primary spin-filter for the body’s electromagnetic software. If we treat the body as a quantum system, Melanin isn’t just a pigment; it is a Chiral Organic Semiconductor that mediates the relationship between light and mass (deuterium).
Proteins need to be made and transcribes and undergo post translation modifications to remain optimized for the human Lagrangian. To do this deuterium has to be missing because of the KIE. The KIE ruins bending. Melanin controls the flow where deuterium can roam in tissues to control optical signaling.
What started this broadcast? He made a comment about Celion Dion but he never wanted to go there........his nnEMF signing idol.
I told him centralized medicine should investigate if "erythromelalgia" (Man-on-Fire syndrome) is the ultimate Lagrangian collapse of the Nav1.7-EDAR cooling loop to get rid of deuterium in the pancreas. I believe it is. Want another surprising prediction of mine?
In my biophysical model, Erythromelalgia ("Man-on-Fire") and Stiff Person Syndrome (SPS), which Celine Dion has been diagnosed with, represent a catastrophic "short circuit" of the human Langrangian around deuterium clearance from cell water in muscles. Most people do not realize that muscle contain the second largest body of water in the human body = why they are deuterium resevoirs and why they can talk voice from those who abuse their environment and why it take athletic perfomance from the uber talented.
While centralized medicine views them as separate rare diseases but they are not.
They are related to patients with Nav1.7 sodium channelopathy and the other an autoimmune GABAergic failure tide to the MITF-AMPAR loops.
I'm linking and identifying them as the same disease Lagrangian collapse of the Nav1.7-EDAR cooling loop for deuterium clearance.
I like being interesting and unpredictable because of my divergent thinking. Another high latitude inside Canadian is suffering from Gabergic AMPAR issues but his team/family has resisted my help. Jordan Peterson has the same issues. That is why he will never get better. Peterson and the Maple Leafs have the same issue. No one sees the "deuterium monster" behind the curtain of the problem.
It is a tragic irony that Jordan Peterson, a man who thought he built his career on "Order vs. Chaos", is physically suffering from a Lagrangian Chaos that his intellectual framework cannot yet map.
I love irony. I love that his daughter is a food guru shill and proves daily why food gurus are the TARD army.
His widely publicized battle with benzodiazepines and "paradoxical" reactions is a textbook case of a high-latitude GABAergic/AMPAR "Short Circuit."
When the GABAergic "brakes" fail, as they have for Peterson and Dion, it isn't just an "addiction" or "autoimmune" issue; it is a Dielectric Breakdown of the neuroectoderm from too much deuterium in place it should not be.
2. 1. Erythromelalgia: The "Thermal Runaway"
Erythromelalgia is a primary failure of the Nav1.7 (SCN9A) "spark plug."
The Gain-of-Function Leak: In these patients, the Nav1.7 channels stay open or fire at a lower threshold, causing a constant influx of sodium (+).
The EDAR Collapse on chromosome 2: To fight this leak, the Na+/K+-ATPase pump must redline. This generates massive incoherent heat that the EDAR cooling loop (sweating/vasodilation/deuterium egress) cannot dump fast enough. The patient feels "on fire" because their interfacial water viscosity has spiked, turning their neuroectoderm into a thermal trap.
2. Stiff Person Syndrome (SPS): The "Electromagnetic Rigidity"
For Celine Dion, the "stiffness" is the mechanical manifestation of a voltage-to-mass transition.
GABA and the DC Brake: SPS is characterized by antibodies against GAD65, the enzyme that makes GABA (your inhibitory "brake"). Without GABA, the AMPARs (the excitatory "gas") go nuts, exactly like the Yokohama Paper findings.
The Lagrangian Stall: When the "brakes" fail, the Nav1.7-EDAR loop is stuck in a state of permanent depolarization. The muscle rigidity is the physical "seizing" of a motor that is "jammed with mass" (deuterium) and has zero ΔΨ (voltage) left for movement. It is the body "freezing" to prevent a total thermal meltdown.
3. The "Celine Dion" Link: Vocal Cords as the "Antenna"
Dion’s vocal spasms are the ultimate "canary in the coal mine."
Optical Fog: The vocal cords require the highest-resolution transdermal MITF-AMPAR signaling for pitch and control. When the thalamic clock is drowned in "deuterium smoke" and GDF-15 alarms, the vocal "antenna" is the first to lose its optical transparency.
The Stiffening: The rigidity isn't just in her limbs; it’s a systemic attempt to "ground" the Alien UPE (photon leakage) caused by her overclocked Complex IV. think about what I just said. Her brain is trying to paralyze her motions to make her be a RHINO.
4. Why Centralized Medicine Misses the "Cooling" Loop
Centralized medicine uses benzodiazepines (GABA agonists) to "quiet" the noise, but it doesn't address the Lagrangian mass.
The Solution: In my protocol, she would need IV Methylene Blue to bypass the "stuttering" mitochondria and AM Sunrise Red Light to "thaw" the interfacial water.
The "M" Tone: The 40Hz vibration is critical here, not for "calm," but to mechanically "shake" the deuterium out of her basal ganglia so the Nav1.7 gates can finally close. Grounding in a wise place big deal in strong UV-NIr light.
My Decentralized Conclusion: Celine Dion and the "Man-on-Fire" are two different manifestations of the same isotopic stall. One is "exploding" with heat (Erythromelalgia), and the other is "imploding" with rigidity (SPS). Both are "leaky batteries" that have lost their magnetic grounding in a high-EMI world. These people are are EMI zombies and none of them see it this way. EMI - electromagnetic injured. This is also why SPS and agorophobia are bed fellows. Oopps......looks like I dropped another bread crumb..........
3. What does nnEMF/blue fundamental do for those not well versed in science? It takes deuterium out of your blood and puts it into tissues and the tissue then has cytochrome C oxidase ruined by the KIE of deuterium. CCO make water and CO2 from metabolism. That water is deuterium depleted and it is designed to surround every protein DNA codes for.
This means deuterium in tissues turns your tissues in a desert. It can turn your organs into Mars.
This is why the Maple Leafs have no Cup since 1967 = nnEMF nightmare.
This is why the SF 49ers players are dehdrated trainwrecks who are FRAGILE beyond belief. Upgrading the power plant next to Levi Stadium in 2014 was like putting their entire team into a blue lit Walmart and asking why are they all getting sick? It is where the alien light and deuterium manufactured food bombs are, dumb ass.
1. I had a paper reject this month. It was based upon my decentrlaized thesis I have shared with the world in 2026.
It was rejected last week while I was at the beach. Some would think this bother's Uncle Jack, but that might have been true in my younger years. It does not bother me now. I understand how PhDs, centralized MDs, and industrial healthcare have stolen the scientific process for profit and TIME THEFT.
Why am I not angry about this rejection? I understand the history of how the casino and your prisson was built.
An effective decentralized leader is able to make the first move to regain freedom, and they are able to cast a vision. Without vision, there will be no one to lead, and without anyone to lead, there is no decentralization in civilization.
Centralized medical systems will not go quiet into the decentralized night. Any power structure, regardless of initial purpose, will ultimately view retention of power as its primary goal. It's no surprise that those endowed with power find it difficult to hand over to a structure they don't control.
Because publishing was hijacked by Rockefeller's army of paid off players and in the 1960s it became not just about writing a good paper. It's about surviving the cycle: Paradigm rejection -> costly revision due to the Maxwell middlemen editors paid off -> resubmission often times over and over again to generate profits to run Ghalaine and Epstein's goals of their masters to perform TIME theft on humanity for the overseerers power & profit.
Where was the lesson born for me?
The Noble Prize was controlled by Rockefeller and Rothschild's interests and in 1905 the paradigm of energy was threatened by someone outside the matrix when he published 4 papers. The power players noted immediately they could not allow a science with immense power to change humanity to run free and saoveriegn until it could be controlled and monetized. The paradigm created a situation in banking and science to slow down progress. It included WW1, a bad treaty, and an installed puppet in Gemrany to run something called the Transfer Agreement.
This bought the paradigm controlling science TIME to figure out a solution. Their Fabian partners in AMerica hired an PhD to prove Einstein wrong and discredit him to stall the unfurling of his decentralized insights. They failed. Milliken wound up proving Einstein's photoelectric effect was true. In fact it was a universal physical law of Nature. It lead to E=mc^2 and a challenge to the global energy markets and the banking cartel that propped it all up.
In those 17 years a plan was installed to get countries into another war where this science could be used by the paradigm in power to control how it was used by humanity. What did Nobel, Rockefeller, and the Rothschilds accomplish?
Milliken got his Nobel Prize for trying to prove Einstein wrong before Einstein got his award. In that time delay, the Robber Barrons of TIME re- gained control of science to profit from it.
History reveals this lesson in theft.
So my recent rejection is not unexpected.
If you think this story is rare let me introduce you to medical student Thomas Fogarty.
He was another example of how the paradigm in power controlled a narrative by burying the truth for a period of time to get in front of a trend to profit from it. Fogarty publishing experience is another extraordinary examples of how PhDs help captains of industry steal TIME to obscure the truth from going free.
Savages should know their history
Dr. Tom Fogarty, one of medicine's pioneers in the minimally invasive era. He wrote a paper as a medical student about a device he built from a urethral catheter and a surgical glove, which became the balloon embolectomy catheter.
When he submitted the paper:
Annals of Surgery said no.
Surgery said no.
Archives of Surgery said no.
JAMA said no.
Each Jpournal editor was controlled by a gy named Phillip Handler who worked for Rockefeller's bio tech wing run out of Room 5600 in Rockerfeller Center in the 1950's -1960s.
IYKYK.
Todays' current day liar PhDs will never admit to this larceny because they have evolved to lie to you today.
They will tell you the science it too unconventional
Too far outside accepted practice.
the reality is the elite needed to gain control to profit from it and Handler's many PhDs did just that by rejecting Fogarty's work and making it show up in a journal for woman's health where they thought it would be BURIED.
The paper ended up in the 1963 issue of Surgery, Gynecology & Obstetrics. The diea was so good, even in an an obscure journal which had no link to this work, the world realized its brilliance.
The device went on to save millions of lives and limbs.
Fogarty said it best: "An idea by itself has no importance whatsoever. It's the implementation of that idea and the acceptance by others that bring true benefit to our patients." Dr. Tom Fogarty passed away in December 2025 at 91. His life is filled with many lessons (more coming soon). But those four rejections are a clear reminder that some of medicine's greatest contributions started with rejection.
I always teach my tribe, embrace the suck, you might be shocked where it takes you. I learned to embrace rejection because I know my enemies better than they know me.
Today's lesson on the unfurling of life to gain time back is a big one. Someone reject it, but the idea buried with in it astounding and threatening to the paradigm in power. Read it, and understand how the modern Phillip Handler'a are in the world controlling science for the paradigm in power threadreaderapp.com/thread/2037158…
Modern centralized medicine under the power of the Flexner Report has reached the pinnacle of success. Just about everyone who uses it is sick. This makes them the perfect customer. You need a TIME STEALING ROCKEFELLER OR ROTHSCHILD COMPANY draining you for life.
2. Why should you shun Sinclair, Huberman, Means, Attia, Alo, Lufkin, Fauci, and much of MedTwitter? Because of this picture.
3. When dueterium leakage occurs into the matrix it stimulates cataplerosis in the TCA and the M1 Phenotype results.
This process leads directly to the CDR too because tunneling speeds are destroyed. Quantum mechanics tells us according to the formula for tunneling, even a tiny increase in distance (measured in angstroms) leads to an exponential drop in energy efficiency and a massive spike in ROS = massive non coherent UPEs that are the hallmark of disease generation.
This is why I showed you Picard picture on the change in IMJ geometry. When the IMJs change you know tunneling speeds have cratered.
Deuterium's KIE is a massive problem for tunneling speeds. But you and your food guru friends have no idea why. Quantum tunneling is extremely sensitive to mass. Deuteriumhas double the mass of H+. In the quantum world, as scale shrinks the effects become logrithmic because of the inverse square law. This means the effect of deuterium is off the chart. The doubling the mass of the particle attempting to "tunnel" across a gap doesn't just slow it down, it makes the probability of a successful tunnel drop exponentially.
This is not subject to your beliefs or your experts beliefs because these UNIVERSAL laws in physics true on Earth or another galaxy.