Category: Uncategorized

What if I was to tell you the two most important biomolecules that do this is dopamine and melatonin, would you believe it? Dopamine derives itself from the breakdown of melanin. Melanin can be made accretively from dopamine as well. This allows life to experience the world as it is not. It provides cells a new lens, a new perspective of what life might be like when additional energy is added to the mix. Ironically, a loss of oxygen is how melanin becomes dopamine. When you turn your attention away from reality, dopamine jumps to action. It allows you to “move beyond the concrete”, to a realm that doesn’t yet exist. It motivates you to pursue, to control, and to possess a universe beyond your immediate grasp.

To make large collections of semiconductive proteins like dopamine and melatonin quantum coherent you need to link them together electrically.  Melanin does this for mammals.  Melanin in your skin and neuroectoderm conduct DC electricity.  This is what links these biomolecules.

Melanin is the master semiconductive protein in mammals. Dopamine can be the child of melanin degradation. But melanin can be made accretively from dopamine as well. It is a bidirectional pathway in mammals. Dopamine can be made many ways by mammals. This neurotransmitter is often referred to as the “reward molecule”. From my vantage point, life in the primate clade is based around the thrill of the chase, the anticipation of something new, and the excitement of getting something that’s novel and unexpected. It is what really gets our molecules buzzing.

IS MITOCHONDRIA: METABOLISM LINKED TO MELANIN RENOVATION ENDOGENOUSLY?

Dopamine and melatonin have to be linked electrically to become coherent. This tells us that there should be a deep tie in mitchondrial metabolism and the electrical coupling of dopamine and melatonin. What is it?

Amano et al. (cite 4) have provided a theoretical framework that demonstrates that resting tremor and other motor behaviors seen in Parkinson’s Disease are actually metabolically energy efficient. They posit that the role of dopamine, which can be a precursor to the formation of neuromelanin, and energy metabolism in the brain is linked and supported this assertion with research finding that “dopamine lesions result in reduced glucose uptake,” showing a preservation of energy, and dopamine is related to glucose metabolism. They conclude, “the loss of dopamine neurons in Parkinson’s Disease is likely to contribute to dysfunctional glucose metabolism.” Ironically none of them have made the link to why red light lowers blood glucose by 27% nor why when melanin is missing in cells endogenously, cells lose their ROS generation power from mitochondrial metabolism.

It appears that ROS and a lack of redlight production in mitochondria maybe the key link in diseases associated with altered glucose metabolism. They also note the growing amount of literature arguing mitochondrial dysfunction is common in Parkinson’s Disease and is causing metabolic dysfunction. They went on to say that they have discovered that there is an inverse relationship between melanin levels and mitochondrial ATP production. In fact, it appeared to them that melanin may hold the primary supply of energy while mitochondria produce supplemental energy, in an opposing, but complimentary, interdependent relationship.

BACK TO SUPERPOSITION OF DOPAMINE. MELATONIN, AND MELANIN

In quantum science, objects such as electrons and photons have wavelike properties that can combine and become what is called superposed. Particles are not the only thing that can be superposed. So can whole atoms. Did you know that this ability in quantum mechanics is not limited to just atoms either.

Complex molecules can be superposed.

Many have heard about many world interpretations verison of quantum mechanics. Very few have heard about many world chemicals that are capable of staying in superposition to deliver different possibilities and outcomes in Nature.

Physicists have now proven any chunk of matter can also occupy two places at once. Physicists call this phenomenon “quantum superposition,” and for decades, they have demonstrated it using small particles. But in recent years, physicists have scaled up their experiments, demonstrating quantum superposition using larger and larger particles.

The double-slit experiment reveals the central puzzles of the decentralized systems in quantum mechanics, putting us ‘up against the paradoxes and mysteries and peculiarities of nature”.

Researchers had long known that light, fired through a sheet with two slits in it, would create an interference pattern, or a series of light and dark fringes, on the wall behind the sheet. But light was understood as a massless wave, not something made of particles, so this wasn’t surprising. However, in a series of famous experiments in the 1920s, physicists showed that electrons fired through thin films or crystals would behave in a similar way, forming patterns like light does on the wall behind the diffracting material.

If electrons were simply particles, and so could occupy only one point in space at a time, they would form two strips, roughly the shape of the slits, on the wall behind the film or crystal. But instead, the electrons hit that wall in complex patterns suggesting the electrons had  interfered with themselves . That is a telltale sign of a wave; in some spots, the peaks of the waves coincide, creating brighter regions, while in other spots, the peaks coincide with troughs, so the two cancel each other out and create a dark region. Because physicists already knew that electrons had mass and were definitely particles, the experiment showed that matter acts both as individual particles and as waves.

But it’s one thing to create an interference pattern with electrons. Doing it with giant molecules is a lot trickier. Bigger molecules have less-easily detected waves, because more massive objects have shorter wavelengths that can lead to barely-perceptible interference patterns. And these 2,000-atom particles have wavelengths smaller than the diameter of a single hydrogen atom, so their interference pattern is much less dramatic.

To pull off the double-slit experiment for big things, the researchers built a machine that could fire a beam of molecules (hulking things called “oligo-tetraphenylporphyrins enriched with fluoroalkylsulfanyl chains,” some more than 25,000 times the mass of a simple hydrogen atom) through a series of grates and sheets bearing multiple slits. Recall cells are filled with porphyrins like the two below.

In the experiment in Cite #1, the beam was about 6.5 feet long. That’s big enough that the researchers had to account for factors like gravity and the rotation of the Earth in designing the beam emitter. They also kept the molecules fairly warm for a quantum physics experiment, so they had to account for heat jostling the particles.

When the researchers switched the machine on, the detectors at the far end of the beam revealed an interference pattern like we see with electrons. In fact, the molecules being studied were clearly occupying multiple points in space at once. This means large biomolecules can and do act like electrons do. They do have a superposed ability.

It’s an exciting result, for quantum biology, proving quantum interference at larger scales is possible. This was the first time in history this has been detected.

 

SUMMARY

The implications of this endogenous ability in chemicals is the basis of how MOLECULAR RESONACE operates. Molecular resonance is a quantum mechanical characteristic of all matter. This ABILITY is inherently BUILT into how REALITY is perceived. It is buried inside of the chemicals that cells have chosen to use through evolutionary timescales.

The most important biomolecules are coded for by DNA. DNA seems to favor biomolecules that have specific semiconductive and optical characteristics in their absorption and emission spectra. The design process of cellular life begins with the DNA code.   Centralized biology today is a detailed, disorganized collection of disparate facts. It is like a hoarder’s basement, or a rat’s nest. There is no decentralized connecting design of what is buried in DNA’s code. You can scoop up a bag full of facts and try to make sense of it, but that would be an exercise in futility. True wisdom is fractal and non linear. The design can be complex, with microscopic details, but the overall design is coherent and beautiful.  To make large collections of semiconductive proteins quantum coherent you need to link them together electrically.

We do this PHOTOELECTRICALLY.  This idea implies that cells have some electric tuning ability built into their protein structure.

It appears the choice is related to the spectrum of light that interacts with them. Possibilities and probabilities for life is made tunable just by changing the incident light photons. That is how these chemicals all operate. This implies that your mitochondrial metabolism creates an adaptable light spectrum during metabolism and it is this light that tunes and controls the chemicals in you to act in different ways.

A dopamine molecule consists of a catechol structure (a benzene ring with two hydroxyl side groups) with one amine group attached via an ethyl chain. The amine part of the ring contains nitrogen. If you draw the two possible Kekulé structures for benzene (pic below), you will know that the real structure of benzene isn’t like either of them. The molecular structure acts like it is capable of being in two states.

The two structures above for benzene’s ring are known as canonical forms, and they can each be thought of as adding some knowledge to the real structure. For example, the bond drawn at the top right of the molecule is neither truly single or double, but somewhere in between. Similarly with all the other bonds. The real structure is somewhere between the two – all the bonds are identical and somewhere between single and double in character.

Benzene two structures also sit in a superposed position. That’s because of the electron delocalization in the benzene ring. The aromatic rings of carbon in benzene are the playground for bio- photons as the picture below shows. Those benzene rings capture the photons and tune it.

As such, dopamine is the simplest possible catecholamine, a family that also includes the neurotransmitters norepinephrine and epinephrine.

If we take the two forms as the picture above shows perhaps the two most important ones, it suggests that there is delocalization of the electrons over the whole structure of the 6 carbon ring. With dopamine above, that electron density is a bit low around the nitrogen atom carrying the positive charge on one canonical form or the other. Any canonical form that you draw that shows nitrogen close to the ring, it follows that another atom must balance that charge. In dopamine that atom is oxygen at the 7 and 10 o’clock positions. Where the charge change occurs changes the absorption and emission spectra of dopamine. Separating negative and positive charges in this fashion is thermodynamically unfavorable. This is how tunability occurs with charge separation in a benzene ring. Light tunes molecules by altering their charges. This is why all the aromatic amino acids have benzene rings in their molecules. This also happens in methylene blue.

HOW DO YOU CREATE YOUR INNER MASTERPIECE?   YOUR CHOICES DICTATE THAT PATH

Dopamine controls the process of choice and action. Nothing EXCELLENT ever happens without EXECUTION. No masterpiece has ever been made by INTENTION alone. EXECUTION takes INITIATIVE and INTELLIGENCE. EXECUTION is the antidote to PROCRASTINATION. Ideation without execution leads to deletion of any idea. A poor idea executed accomplishes more than a great idea that stays locked away in a person’s head.  This blog is exploring how the small changes in light can affect change in your brain.  Actions end superposition. Actions – executions of ideas. EXECUTION calls off the fence of indecision and put us in the valley of decision; it calls us off the bench and onto the field. It does matter how much talent you have as a player in your life, but that talent is useless with inaction because you can never score a goal while you’re on the bench. That is how dopamine is the molecule of more for mammals.

This idea explains to us how dopamine can do all the things it is capable of doing without a lot of modifications we can observe biochemically. Dopamine drives you to seek out things far away, both physical, things you are blinded to, such as love, sex, wisdom, and power. Changing your ultraweal biophoton signature and shining it onto dopamine in certain circuits allows you to put hot sauce on your dinner, think about building rockets to fly to the moon, worshipping a God in the sky, beyind the space and time frames you live in. This chemical appears to have unlimited abiliities to bring to your life endless possibilities over any distance, whether that distance is intellectually or geographical. In your brain’s quantum computer, dopamine has become a single molecule that is the ultimate evolutionary handy tool. It is what moved us past Neanderthals, and began to urge us, through multiple tracts in our brains to move beyond the pleasure of just being, into exploring the cosmos of possibilities that come into focus when we imagine. Every creature on Earth has dopamine and melatonin in their cells, but no creature has more of them then humans. Madness and genius both depend on how dopamine is programmed by light. This tells you dopamine itself is capable of superposition. This idea also underpins this cliche as well. Talent hits targets no one else can hit; but genius hits targets no one else can even see.

I think this idea extends to chiral molecules in biology. DNA is made up of chiral molecules. Matter-wave diffraction patterns can put chiral molecules into superpositions of left- and right-handed forms. Experiments have already shown it and this will enabling new studies to be done of how the two states interact with their environment to give two different outcomes.

Small chiral molecules such as amino acids and sugars are the building blocks of larger molecules, such as proteins and nucleic acids, which are also chiral. A chiral molecule and its mirror image are called enantiomers; one is dextrorotatory (D) and the other is levorotatory (L). This is another way evolution likely happens that is also a break with Darwinism.

Most of you know I think this guy in the Tweet is a Twit when it comes to science. But even a blind squirrel is able to tell time correctly twice a day. Listen carefully what he says about Neanderthals and what I have told you about dopamine and creatitivity in this series already.

https://x.com/got_cake/status/1791306643809980457

Semiconductive quantum dots (QDs) have been widely used for fluorescent labelling in modern experiments. However, their ability to transfer electrons and holes to biomolecules leads to spectral changes and effects on living systems that have yet to be exploited in centralized science. Cells appear to do this easily.

How do I envision how this operates in us?

Quantum Dot-dopamine conjugates can be used to label living cells in a redox-sensitive pattern: under reducing conditions, fluorescence is only seen in the cell periphery and lysosomes. As the cell becomes more oxidized, Quantum Dot labelling appears mostly in the perinuclear region of cells. This would include in or on surrounding mitochondria where biophotons are created metabolically.

With the most-oxidizing cellular conditions, Quantum dot labelling throughout the cell is seen already in experiments. Thee experiments have taught us phototoxicity results from the creation of singlet oxygen, and it can be reduced with antioxidants. Melatonin is the major antioxidant inside the cell created by mitochondria to manage this process. there are many small molecule proteins liberated from mitochondria that could do this. When you comprehend what I am proposing here this picture below should have new meaning. It shows you how reality is perceived and how it can be changed rather easily. This explains how dopamine can build creativity, madness and genius in humans and how its creation can vary in one single life to explain what happened as Jimi Henrdrix, Kurt Cobain, or Jackson Pollack aged in their lives.

The living universe selects for maximum entropy, and minimum waste heat. Melanin was critical in evolution of bringing biological complexity to the interior of mammals.

In this context, the melanin universe in mammals can and should be seen as a self-organizing system that seeks to optimize its energy use and minimize waste heat. This is reflected in the emergence of complex structures and patterns in the universe, from the formation of galaxies and stars to the development of dopamine, and life on Earth.

The universe and cells have much in common. Both are decentralized systems.

The idea that the a cell and the universe are self-organizing systems that seeks to maximize entropy and minimize waste heat has far-reaching implications for our understanding of life and the universe and our place within it. It suggests that the universe is a dynamic and ever-changing system that is constantly seeking to optimize its energy use and maximize its complexity. It also suggests that tissues, collection of cells have the same ability buried within them.

Dopamine narrates your life and it is the main story teller of how life came to be within the primate clade in evolution.

CITES

1. https://www.nature.com/articles/s41567-019-0663-9.epdf

2. https://wires.onlinelibrary.wiley.com/doi/full/10.1002/wcms.1640

3. B. A. Stickler et al., “Enantiomer superpositions from matter-wave interference of chiral molecules,” Phys. Rev. X 11, 031056 (2021).

4. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285053/

The Melanin Renovation Rx is based on Noether’s theorem, which is the key missing piece. The theory states that every differentiable symmetry of the action of a physical system with conservative forces has a corresponding conservation law. The symmetry in the mammalian physical system is based on UV light. Time symmetry implies energy conservation. So, what happens to mammals when they lose energy? They lose time symmetry. In other words, time flows differently backward and forward. There was a time on early Earth that the TCA cycle only flowed counterclockwise because there was not a lot of oxygen or as much UV light around.

It sounds incompressible and unimportant until I remind you of what you just learned about the TCA cycle in the last few blogs. In modern times, biochemists are familiar with it running forward clockwise with plentiful oxygen and sunlight is pumped into the system every AM, and it rotates counterclockwise when these conditions are not met. The implications of this rotational symmetry change are enormous for you understanding. Why? Your time experience varies depending on the direction of the spin of this cycle in your cells. Sounds crazy doesn’t it?

Theories of criticality in physics have been successfully applied to biology. The mathematical core of these theories rests upon the idea that a “phase transition,” which can be either critical or not, may be described as a point along the line where the intended control parameter runs. For example, the ferromagnetic/paramagnetic transition of iron and oxygen takes place for a precise temperature value, the Curie temperature.

Remember that light and temperature control the entropy flow in your circadian clock mechanism. When you realize this, you might begin to see how people experience time differently in their lives

If you paid close attention to the video above, you’d have heard that energy conservation implies time symmetry. It also follows that anytime there is a violation of time symmetry, the energy conservation of the system has been violated in some fashion. This happens when mtDNA is altered, melanin is lost, or water is not created in cells from metabolism. All of these things change oxygen tensions inside of cells as a result. All these things cause our cells to liberate more light than we should. This light liberation changes the AMO physics in mitochondria. That is what the ROS and RNS signal tells the decentralized clinician. These ideas are all buried in the slide below.

What facts about Nature isn’t in the slide above? Most centralized scientist believe ROS is associated negatively with cell function. It just is not true. ROS is not inherently negative for cell function; instead, it plays a complex role in regulating various cellular QUANTUM processes that centralized biology has not stumbled upon yet. The interplay between ROS, endogenous biophoton creation, and low intensity laser creation inside of cells offers opportunities for the centralized audience to rethink their beliefs and approaches to understanding cell biology. Most of centralized science has no idea that cellular conditions involving elevated ROS production (chronic diseases like diabetes) are associated with increased low-intensity light therapy sensitivity. The reason is quite simple. Diabetic tissues have lost most of the sotred photonic energy at the electronic and vibrational levels in cells. Diabetic cells emit higher amounts of biophotons to their environment in an attempt to raise their own ROS to actually stimulate higher ATP production. The problem is oxygen tensions in diabetics is low, along with biophoton power and intensity so that endogenous light production for regeneration becomes improbable. The detection of biophotons is now well established in the biophysical literature, is also associated with the production of ROS and the cellular redox state. Low intensity light therapy via PBM which mimics what red light from the solar spectrum normally gives the semiconductors in cells. This light also has the potential to induce cellular effects through accelerated ATP production. This paper here: HYPERLINK should blow your socks off. When I read it in 2010 I was stunned.

Humans no longer live in the light this mechanism is designed to work with. This is a big part of why we have chronic disease epidemics that we do today. Few see how light is the driver of the entire process. By the time this blog is done, I think you will have enough data to show you why I am adamant that light trumps food at all the most critical levels in cells.

WHY DOES COLD HELP MAMMALS ALSO CONSERVE TIME?

When the temperature decreases and passes through that point, the magnetic orientation organizes along one direction, and magnetism appears. When the temperature increases through that point, disorder prevails, and magnetism disappears. Magnetism emerges from the system’s atomic-molecular organization. Think of mitochondrions as organelles that create paramagnetic chemicals (free radicals) by altering the atomic lattice of atoms fed into it. Most of the atoms fed into mitochondria are not paramagnetic. Many of the atoms that come from mitochondria have distinct magnetic fingerprints. Those fingerprints emerge from alterations of the AMO physics that are occurring inside the organelle.

Mammals’ criticality begins with UV light because it works with mtDNA, quantum dots, and melanin to create VUV-IR light inside a cell. When the critical amount of these entities goes missing inside mammals, they suffer a loss of healthspan or a loss of time. Their TCA cycle does not spend most of its time spinning in a clockwise fashion. When they get enough AM light, and sunlight during the day, they become robust and antifragile because the TCA cycle is operating as it should. When they do not, they get sick and die sooner than they should.

The TCA cycle highlights this time symmetry idea. The same biochemical pathway is used to create and destroy cells. I have told you many times that everything can and should be thought of as a clock. That is clearly how Nature views the TCA cycle when you view it from this perspective.

Very recently in this series of blogs I told you about an experiment in 2012 that showed us that the laws of physics are not time symmetric. It was buried from most people’s awareness because the experiment occurred at the same time the Higgs boson was discovered. Prior to this 2012 experiment, centralized science believed, that whether you run “a clock” forward or backward, most believed the laws of physics to be the same because of Noether’s theorem. The 2012 experiment showed us otherwise and I became quite happy because it explained to me really what the TCA cycle was doing and why mammals lose light when the TCA cycle is spinning counterclockwise. During this shift in time, we should expect a change in energy based on the relationship of conservation laws to time time symmetry. That was the point of showing you the video above. The TCA cycle is a cell’s difficulty adjustment in how it tells time. I want you to understand that when time is the currency in question, energy has to be expended and it is lost to the environment. When this happens aging manifests. This is truly how time is created in biological systems based on a proof of work mechanism.

This concept of time is funda­mental to our way of thinking. It is derived from the more basic concept of the order in which events occur. Given the perspective I am trying to show you, I want you to ask yourself the following questions. Who or what should be in charge of time if putting someone in charge is not allowed in the system? How can you have a reliable clock if there is no central frame of refer­ence? The key here is to understand in your cell, a mitochondria is the time machine that houses this TCA clock. That TCA cycle mimics a difficulty adjustment in the cell. Can I just make energy or do I have to make things I need to operate my cell? Got it? How that clock works is based on how often it senses the sunrise in its environment. I have brought this message to social media for 20 years.

AMO PHYSICS INSIDE OF THE MITOCHONDRIA IS CRITICAL

This criticality of this idea scales and corresponds to the appearance of a “coherent structure” in mammalian cells, that is, space and/or time correlations at all scales, which at the transition point (melanin renovation point) give a “global” aspect to the new physical object. These ideas are pretty relevant to analyzing quantum actions buried within biological organisms.

Melanin is critical in maintaining the AMO physical organization of the mitochondria and the functioning of the TCA cycle. Why? Melanin is only translated from its parent gene when UV light is present in the mammalian environment and or its tissue. This point cannot be magnified enough of how critical this relationship is to light. No other gene is linked to smallest part fo the visible spectrum of the sun and this same frequency of light is linked to every single biophoton cells release. It is a remarkable connection in nature that has gone unnoticed by centralized science.

Biological systems, on the other hand, exhibit criticality across multiple parameters such as genetic variations, environmental changes, and interactions with other organisms. This ongoing criticality allows for flexibility and adaptability in response to changing conditions, ensuring the survival and evolution of the organism.

Furthermore, the concept of criticality in biology extends beyond individual organisms to entire ecosystems. Ecosystems are complex networks of interacting species and environmental factors, and their stability and resilience are maintained through a delicate balance of interactions. When this balance is disrupted, it can lead to catastrophic shifts in the ecosystem, such as species extinctions or ecosystem collapse.

Overall, the concept of criticality in biology highlights the dynamic and adaptive nature of living systems, and underscores the importance of studying and understanding the complex interactions that govern biological processes. By recognizing and studying critical transitions in biological systems, we can better understand how organisms and ecosystems respond to environmental changes and potentially develop strategies for conservation and management.

Circadian control in a tissue is an ideal example of how biology builds its most important criticality.  Its efficiency is correlated with mitochondrial redox power between -440meV to -200MeV.  Outside this “critical” zone, life has problems.  Without the maintenance of this redox zone, the clock within the time machine is altered, and mammalian health metrics fall apart.

I submit to you that both of the pictures above are showing you Nature’s recipe for time buried in living systems. The first picture you are well acquainted with if you are a scientist. The second one is for mathematicians which also shows how light time shifts mammalian longevity.

Life solves this problem by re-inventing time itself. It says no to seconds and yes to mitochondria to create its own version of biological time stamping in cells. All clocks rely on periodic processes, something that we might call a “tick.” Mitochondrial periodicity is linked to AM sunrise and this begins the “tock” that clicks in the TCA cycle. The frequency of your clock — how often it ticks — depends on its use-case with the light choices you make. Your clock is an atomic optical lattice clock.

Most clocks you are familiar with have a fixed frequency. After all, we want to know the time precisely when we are going to a meeting or a class. There are, however, clocks that have a variable frequency. Your circadian clocks are based on the variable frequencies of how the sun changes in a day. Those clocks are called metronomes. A metronome has a variable frequency that you can set before you make it tick. While a metronome keeps its pace constant once it is set. This is why AM sunlight is irreplaceable in humans. It sets the pace for the TCA cycle. This makes the TCA act like a difficulty adjust knob in the clock.

While time causality is essen­tial in biochemical pathways, it is not suffi­cient to explain biological time keeping. This is why we have molecular clocks. They focus on time causality. The more counterintuitive reality of timing in the mitochondria is that they need unpredictability to work well. Why do we need two ways of handling time? It turns out we need unpre­dictability for time to flow for our quantum realm in cells. In the physical realm, we observe natural processes to describe the flow of time. We observe a general increase in entropy and call that the arrow of time. Even though the laws of nature seem to be obliv­ious in regards to the direc­tion of this arrow in most cases, certain things can’t be undone, practi­cally speaking. You can’t unscramble an egg, for example..

Similarly, entropy-increasing functions are required to estab­lish an arrow of time in the quantum realm in mitochondria where subatomic particles are being used for timing. Just like it is practi­cally impos­sible to unscramble an egg, it is practi­cally impos­sible to unscramble the epigenetic signa­tures that control the genome. When timing is off in your mitochondria that is precisely what happens to your DNA and that is what causes genomic shifts in cancer.

In biology, the proof-of-work mechanism is physi­cally linked to what happened directly with the sun that day. It is not just a record of an event — it is the event itself.

Without this controlled increase in entropy in cells, we could go forward and backward in time without consequence. Cells rely upon two sources of unpre­dictability: biochemical reac­tion times and the proof-of-work mechanism in sunlight’s energy. Just like nobody can predict what your Twitter feed will look like tomorrow, nobody can predict what the next human offspring will look like in the future either. This is what powers evolutionary change. This is how biological timestamping operates. It is not the world Darwin saw. It is a quantum mechanical process that uses light to create a ledger of time we call life. How is that for a new way to look at yourself?

SUMMARY

In a mitochondria, all we have is subatomic particles which contain data from our environment. It should follow then, that the biological realm is infor­ma­tional in nature, the obvious conclu­sion is that compu­ta­tion is all we have. If your world is made of data, manip­u­la­tion of data is all there is. This is why Nature built a mitochondria after endosymbiosis. She needed a time machine to make complex life.

Proof-of-work works in Nature-to-cell setting because it is trust­less, and it is trust­less because it is discon­nected from all superfluous inputs — such as the readings of clocks, food, your family’s opinions, or the narrative of social media. It relies on one thing and one thing only: compu­ta­tion requires work, and in our universe, work requires energy and time. The brilliant thing about cell biology’s proof-of-work mechanism is that it creates its own reality, along with its own space and time.

Einstein proved time is relative, and simul­taneity is nonex­is­tent. This fact alone makes all timestamps — especially across large distances like we have in biology — inher­ently unreli­able. This is why the SCN needs to be time stamped every morning by AM sunlight. It is also why your iPhone needs to update its GPS coordinates to work. It also explains fully why timestamps of GPS satel­lites have to be adjusted constantly, by humans on the surfaces of Earth to make tech gear operate properly. For life, biological timestamping has to be very precise to maintain health. If it is not chronic disease is the result. This is why evolution built the TCA cycle to function in spontaneous fashion. See Nick Lane’s picture below. Nick still has not figured out why Nature did this.

The reason was simple. Life has to be costly in time and not in energy. The TCA cycle is the diffi­culty-adjust­ment in cells. It’s evolutionary function is about keeping a constant time in cells, not a constant level of immunity in all tissues or in energy expen­di­ture. We know the TCA cycle varies its energy production in various tissues. Using the TCA cycle spin was an ingenious early step in evolutionary design because longevity has to be costly in time, not energy. Time is the most valuable asset in Nature because it has a fixed quantity. Energy can be sourced in many ways quantum mechanically by cells. if you are understanding this blog well now, Noether’s theorem says that energy conservation is LINKED to time symmetry. This means that every improve­ment in energy gener­a­tion in cells over evolution would allow life to create time. Time is the only thing cells cannot make more of. They became able to build complexity because they began to harvest more energy from the environment. That is what the picture above Nick’s head really says, but Nick is yet to realize it. I hope you do now too.

Nick Lane is correct that understanding why the TCA cycle underpins life is a great mystery to be solved. I am giving you my solution in this blog. It has been in my head for 20 years. The TCA is the biological diffi­culty adjust­ment life needs because it is essen­tial as some of the amino acids its uses.

Because, without it, the internal clock of mitochondra would tend to go faster and faster as more biochemical pathways join the biological network in cells. It would speed up biosynthesis pathways we use to create offsprings via sex. We would quickly run into the coordi­na­tion problem that mitochondria was built to solve as evolution’s time machine. Cancer is this coordination problem. This is why light stress increases ATP production. ATP production is telling us something about the NAD+ to oxygen difficulty adjustment in mitochondria. Something is awry in our quantum timing mechanism. This story goes way back in the blogs. Don’t believe me? READ IT.  Note the date. The ideas in that blog began in my head in 2000-2004. You likely never saw it this way before today.

By viewing living entities as extended critical transitions, we can see them as dynamic systems that continually renew and adapt their structure. This perspective allows us to understand the complexity of biological processes in a new light, recognizing that they are not just static phenomena, but rather evolving and changing systems. This can help us overcome the challenge of analyzing the intricate and nuanced nature of living matter, providing a framework for studying and understanding biology in a more interconnected way. This is the idea buried deep in the QUILT document.  Ultimately, this change in perspective from physics to biology offers new insights and approaches to unraveling the mysteries of life.

There is a very common belief in humans in a divine force or energy that gives life to all living beings has been prevalent throughout human history and has shaped the way we view life and existence. It has provided a framework for understanding the purpose and meaning of life, as well as guiding moral and ethical behavior.

The concept of life as a gift from a higher power has been a source of comfort and hope for many people, offering a sense of purpose and belonging in a vast and often mysterious universe. It has also served as a basis for the belief in an afterlife or continuation of the soul after death, providing solace in the face of mortality.

While the scientific understanding of life has evolved and advanced over time, the religious and spiritual concept of life as a divine gift remains a powerful and enduring belief for many people around the world. It continues to shape our values, beliefs, and behaviors, influencing how we live our lives and how we view the world around us. Ultimately, the concept of life as a sacred and precious gift reminds us to cherish and respect all living beings, and to strive for a more harmonious and interconnected existence.

Some argue that the theory of evolution through natural selection contradicts the second law of thermodynamics, which states that entropy, or disorder, in a closed system will always increase over time. They claim that the complexity and organization seen in living organisms goes against this principle, as it suggests a decrease in entropy rather than an increase.

However, proponents of evolution point out that the Earth is not a closed system, but receives energy from the sun, allowing for the increase in complexity and organization seen in living organisms. They argue that the second law of thermodynamics applies to isolated systems, not open ones like the Earth.

Ultimately, the debate over evolution and thermodynamics continues to be a contentious issue, with both sides presenting compelling arguments. However, many scientists and scholars maintain that there is no inherent contradiction between the two concepts, and that they can be reconciled within the framework of modern scientific understanding.

As yourself this question: Is life a property of matter that does not naturally exist? Might life be a phase of matter that we invented with the help of the environment. On the most fundamental level, all matter that exists is just an arrangement of atoms and their constituent particles, is it not?

This perspective challenges the traditional notion of life as a distinct and separate concept. Instead, it suggests that life is simply a human construct used to categorize certain arrangements of matter. This mindset can lead to a greater appreciation of the interconnectedness and complexity of the universe, blurring the lines between living and non-living entities. It invites us to question our assumptions about what it means to be alive and opens up new possibilities for understanding the nature of existence.

Are mammals/humans, for instance, a bag of special water filled with 26-element human molecules that has been synthesized, by the operation of universe, over the course of the last 13.7 billion years? Or is this something more to this reductionist view point?

Living entities are not “just” processes but something more: they are lasting, extended critical transitions, always transient toward a continually renewed AMO structure. In general, physical processes do not change fundamental symmetries; to the contrary, they are primarily meant to preserve them.

Living organisms exhibit emergent properties (quantum mechanical) that cannot be fully explained or understood by simply breaking them down into their molecular components. The photomolecular effect is one example. These properties arise from the interactions and relationships between molecules and cells, and they give rise to the incredible diversity and complexity seen in the natural world.

Therefore, while it is important to recognize the fundamental chemical and molecular basis of life, it is also crucial to appreciate the complexity and emergent properties that make living organisms more than just the sum of their parts.

From Nature’s view, the world should be seen as only connec­tions, nothing else. Everything is based on probability and nothing is based on cause and effect. This is the perspective of this decentralized quantum biologist.

^^^^This is cite #7.

CITES

 

1. Principles in Geology, by Charles Lyell, 1868.

2. The Origin of Species, by Charles Darwin, 1859

3. http://www.staroceans.org/e-book/Haber_Stornetta.pdf

4.  https://www.math.columbia.edu/~bayer/papers/Timestamp_BHS93.pdf

5. https://medium.com/codex/power-of-merkle-trees-1e44819e9639

6. https://stephanlivera.com/episode/313/

7. https://www.nature.com/articles/s43587-024-00619-x4

Listen to the video and you’ll get one level of complexity. The blog below will give you a new perspective to see on the same topic.

Stoping light in cells is a feature of cellular design and not a bug.

Cellular stress increases bio-photon release, why?

Prokaryotes release 5000 time more light than eukaryotes. Eukaryotes release more light when they are stressed. Do eukaryotic cells use this excess light in some way we do not yet understand?

Yes, I believe they do. It has to do with biological chip design on the topological insulator chips inside of cells.  It is a process of biological photolithography.

Manipulating the flow of light in a material at small scales is a specialty of cells loaded with hydrated carbon-based semiconductors.  Why?  Doing so allows for complexity development under low-power situations.   In a semiconductor, electrons can, in principle, move freely, but an external magnetic field can stop this motion. The circular movement of the ATPase caused by the magnetic field stops conduction, and as such, electrons can only exist in the material if they have very specific energies. The energy level corresponds to the light frequencies that excite these electrons by the photoelectric effect.  These energy levels are called Landau levels, and they are characteristics of electrons operating in a magnetic field.  These forces are operating right around the mitochondria creating a force field of action that allows for quantum mechanical process life needs.  You must open your eyes to new data to see the magic inside of cells.

NATURE’S MAGNETS ARE IONS EJECTED FROM THE CORE OF STARS.

This implies that all biological magnets used in mitochondria and cells come from things that make light. This is axiomatic and critical in showing how physics trumps biochemistry in controlling how life unfolds below the cell level.

Since manganese has a nuclear spin of 5/2 and a nuclear magnetic moment of 3.4687, spectral lines of Mn II show it has a hyperfine structure (HFS). Manganese has one stable isotope with a mass number of 55. The ground electronic configuration of Mn II is 3d5(6S)4s (Sansonetti & Martin 2005). This specific electronic configuration allows cells to create SOD2 from excess oxygen from mtDNA metabolism.

It reveals the queerest aspects of Nature that remain hidden from the biologists and biochemists. Manganese is not a particularly common element on Earth. It is the 12th most common element in the rocks of Earth. However, where it is concentrated reveals the quantum biological story of the evolution of prokaryotes and their lives before oxygen filled the ionosphere. The most incredible abundance of manganese is ferromanganese nodules and crusts along the ocean floor. Marine chemical processes and microorganisms (prokaryotes) capture dissolved manganese in seawater, which is precipitated on the ocean floor. Once captured, the prokaryotes could use the element to create a spectra and a magnet to drive biology using light DIRECTLY from matter.

It should immediately stimulate your neurons to recall that Prokaryotes emit 5000 times more light than eukaryotes. It would help if you remembered that prokaryotes populated our ocean long before eukaryotes ever appeared on Earth. This mechanism is ancient. It is not holistic! It is not alternative medicine. In fact, it is native biology, and it reveals that centralized science and medicine are the real alternative versions of events created by the minds of man in his labs. It is directly related to the organizational plans buried in Nature.

Shannon’s theory of Information has told us that unusual things make excellent information carriers in computing machines. The ground electronic configuration of Mn II is 3d5(6S)4s, a superb information carrier with evolutionary severe weight. Phosgene is a chemical that puts an acetyl group on the aromatic amino acid tyrosine, and this small biochemical change blocks the electronic transition and blocks the flow of information in mitochondria. It blocks the Mn redox cycling between ESR-silent Mn(III) and ESR-active Mn(II) required for superoxide dismutation. Many people do not know that ESR silent Mn(lll) is the source of many of the critical evolutionary porphyrins of life. High spin Mn(lll) has an electronic configuration 3d4(6S)4s. Nature used the D shell electronic configuration of Mn as her signal for SOD2 production. Let that level of complexity sink in while you still think biochemistry is “the main controller” in your cells.

High spin Mn(III) is the archetypal of such non-Kramers ions. Mono and polynuclear Mn(all) are of central importance in biological systems that use heme-based proteins like SOD2, catalase, and photosystem II, while Mn(III) porphyrins phthalocyanines have been used as building blocks in the construction of molecule-based magnets. This has huge implications for how life operates below the cell level. Soon you’ll learn about that level because it is not in your biology books and not in any medical textbooks. That is how vital Turin’s serendipitous finding was for the Ivory Tower. Some of us already knew biology was driven by changing the electronic configuration of ions using light.

For example life is flexible.  How does QED happen during mechanical deformations in life?  Generally, mechanical deformation stops conduction in semiconductors or topologic insulators like graphene; those type of materials turn into an insulator in this case and consequently the electrons become fixed in their lattice & are bound to Landau levels.

Does like act like electrons since they are linked by the photoelectric effect?  Yes.  A photonic crystal, like cell water, normally consists of a regular—two dimensional—pattern of holes as one would expect to see in a silicon layer on a chip.  Breaking this regularity in water in exactly the right manner will deform the array and consequently lock the photons inside the cell. This is how we create Landau levels for photons.

Implications?  Once you slow light down in a crystal, you can steer it to where you need it.  So, increasing your metabolism increases the biophoton creation in the mitochondria.  Then, cell water captures it and drives it to the biochemical boxcars.  In Landau levels, light waves no longer move; they do not flow through the crystal either but stand still. This shows that the deformation of liquid crystalline water can have a similar effect on photons as a magnetic field on electrons.  By altering the deformation pattern, research has shown you can establish various types of effective magnetic fields in one material.  This can be used to do physiological work. As a result, photons can move through certain parts of the material but not in others. Hence, life seems to have an ability to steer light on a liquid crystalline surface.

Stopping light in its tracks to steer biophotons begins to show us how organs really function on our semiconductive chips built by Nature. The ability to stop light gives cells a new biological ability that mimics on-chip applications. This ability can explain how smells and words can go from sensations to visual imagery in working memory. It likely will explain consciousness, memory, and how holography forms in water.

What does this look like on silicon?

HYPERLINK

Slowing light in water was a critical evolutionary step that existed before Nature invented DNA. Ferrodoxins and aromatic amino acids were in our primative oceans. How did it happen?

How do I see a quantum cell using this physics?

Although a magnetic field doesn’t DIRECTLY affect the photons of light directly, a magnet does distort the medium through which light passes and thereby “bend” the light rays indirectly.  This is used inside of cells where mitochondria and melanin are in close proximity.  Cells take advantage of every option Nature provides it to transform energy.  When oxidative phosphorylation is defective, this adjusts the cell’s stress response like the mammalian DAMP program.

Aging isn’t driven by ROS, as doctors are taught to believe. Many now think it is driven by the DAMP Program. I believe sunlight controls all the DAMP molecules. I believe slowing light down in cells is linked to healthspan and aging. Why do I say this? Aging and cancer share some common origins and hallmarks, such as genomic instability. Sunlight exposure creates genomic stability to quiet epigenetic programming and lower protein turnover in cells. Recent advances indicate that damage-associated molecular pattern molecules (DAMPs) such as high mobility group box 1, histones, S100, and heat shock proteins play location-dependent roles inside and outside the cell.

Mitochondria under stress via the DAMP program respond by transforming more ATP to bend light to compensate for the stress.  Why does it do this?   Light travels through space-time along a geodesic – the shortest possible path between two points on a curved surface.  Making more ATP means the ATPase spins faster than 9000 RPM and this increases the magnetic strength in the cell. This magnetic flux is used to make the stressor hormetic. It drives adaptive changes in cells by altering the epigenome.

SUMMARY

When water superconduction is broken in you due to modern life, you must rely on the rapid recycling of ATP from the pathways I mentioned in the EMF-4 blog.  This means that glycolysis and the PPP will be the metabolism the cell will have to rely on when there is a proton problem.  When you live in a world only powered by ATP, your sleep is the first thing to go south.  Initially, it becomes poor before it totally fails,  and you get diagnosed with sleep apnea.  As it goes on more chronically without proper treatment,  you eventually die from right-sided congestive heart disease and pulmonary hypertension.  Yes, in total sleep failure, you get a specific kind of heart failure preceded by a fatal heart arrhythmia.  This rhythm modern cardiology knows about but still has not made the link to it. I have it because of the loss of water proton conduction.

When your sleep fails, your gene transcription falls off., and your mitochondria are liberating more light than they should and making more ATP than they should. This activates the DAMP program in cells.

The DAMP program provides interaction platforms at molecular levels linked to common hallmarks of aging and cancer. They can act as inducers, sensors, and mediators of stress through individual plasma membrane receptors, intracellular recognition receptors (e.g., advanced glycosylation end product-specific receptors, AIM2-like receptors, RIG-I-like receptors, and NOD1-like receptors, and toll-like receptors), or following endocytic uptake. Thus, the DAMP Hypothesis is novel and complements other theories that explain the features of aging. Aging is not a disease. It is a feature of quantum cell design. DAMPs represent ideal biomarkers of aging and provide an attractive target for interventions in aging and age-associated diseases. DAMP phenotype = a loss of energy at the electronic level in the cell. A loss of energy/information leads to a loss of time in your life.

Chronically pumping in light to cells from the sun allows you to remain in a “zero entropy state” of health.   When quantum timing is off, life dies because it has to rely on ATP regeneration and recycling systems (EMF-4) which are only designed to support non-complex life like Archaea and Eubacteria……not a matrix with a complex nervous system in its head.

Cells that use water superconduction live far from equilibrium all the time. Cells are dissipative forms of plasma that allow for exotic physics to occur daily as light and dark act on the cell.   A zero entropy state defines what a perfect equilibrium is,  in case you are wondering.  Thermal energies, particularly at cellular equilibrium, possess no information potential at all to help biochemical reactants meet and react, whereas an excitation or resonance of a specific frequency at a certain temperature where no other excitation of the same energy exists in a system far from equilibrium  (a cell) not only has just the requisite information to do the work but the inherent power to do it as well.

This power is built into its coherent cytostructural design and not into its mechanistic reactions found in a modern biochemistry textbook. The living organisms’ cytostructure provides the motive force of attraction using the power of semiconduction between appropriate bio-reactive moieties. In turn, this enables efficient energy transfers to take place simultaneously without time ever being a major player in those reactions. In essence, time can stand still in a zero-entropy system because light is not moving inside your cells due to the physics of ions and matter in cells in how they are atomically organized.

When this system gets any disorder (entropy) placed into it, we call this inflammation, randomness, or chaos increase, and the result is a process called aging.  It does appear that order comes with chaos.  This chaos is accounted for in a cell by its telomere length becoming shorter.  The shorter the telomere, the more molecular chaos is present and, hence, the older the living organism is.  This links leptin resistance to aging and shorter telomere lengths.  When life is constructed in a quantum fashion, ‘information’ is not something apart from the energy. It is accounted for in functional design and organization.

CITES

https://www.picardlab.org/uploads/7/7/8/4/77845210/s42255-023-00968-8.pdf

https://www.nature.com/articles/s41566-024-01412-3

https://www.youtube.com/watch?v=IKPC64n_U0s&t=114s

This might be the most important blog I’ll write when it comes to neurosurgery and the genesis of neurological disease generation and regeneration. It will be a grand unifying theory that explains, childhood cancer, autism, and glioma progression in adults.

Robert Becker proposed on basis of his experimental work that living matter behaves as a semiconductor in a wide range of length scales ranging from brain scale to the scale of the entire body. Direct currents flowing only in the preferred direction would be essential for the functioning of the living manner in this framework.  He found these currents in his experiments but could never explain them today, this blog will explore the generation of these currents.

Becker’s injury currents of regeneration were found but no one has explained where the DC comes from. This blog explores the likely source.  FERROELECTRIC POTENTIAL OF THE MITOCHONDRIAL CYTOCHROME PROTEINS.  Ferroelectricity binds all cells in tissues together so they act quantum coherently.

This explains why Becker found the nerve input (DC electric current) was critical in the current of injury.  This bioelectric current is critical. In neurons, water is released every time an action potential is created in a tissue.  Mechanical deformation in tissues generates action potentials in an injury situation.  This would cause water to move within the nervous system.  Water is polarizable by light.  Birefringence is the optical property of a material having a refractive index that depends on the polarization and propagation direction of light.

To generate a DC electric current from light there has to be a way to turn solar light into electricity to link cells in a tissue.  Nature turned to solid-state physics to do this.  She used ferroelectricity to do it.

WHAT IS SOLID-STATE PHYSICS?

Solid-state physics is a branch of physics that deals with practical and theoretical investigations of the properties of solids, such as superconductivity, photoconductivity, and ferromagnetism. In other words, it is that the study of solids, through various methods like crystallography, quantum physics, electromagnetism, and metallurgy. Solid-state physics is the most important branch of condensed matter physics. It helps to investigate how the large-scale properties of solid materials result from their atomic-scale properties. Thus, physics forms a theoretical basis of materials science.  This blog will make the case that decentralized biology really is a solid-state physical problem to be solved for centralized medicine.

One of the basic ideas of the mitochondriac theory of living matter is that various currents, even ionic currents, are quantal currents. The first possibility is that they are Josephson currents (Quantum brain blog) associated with Josephson junctions but already this assumption more or less implies also quantal versions of direct currents. The quantum model for nerve pulse assumes the use of WBG semiconductors that all use non-linear optics (NLO) to communicate and transfer information in many ways always using energy stored at the electronic level of cells.  This allows atoms to be arranged in such a fashion that light stronger than terrestrial sunlight can be used to target melanin in humans to regenerate and renovate their tissues using endogenous generate DC electric current and quantal ionic currents through the cell membranes where DHA dominates physiological function.  These currents will act like Josephson currents, making the situation automatically stationary.

One can criticize this assumption since the Compton length of ions for the ordinary value of the Planck constant is so small that magnetic flux tubes carrying the current through the membrane look rather long in this length scale. Therefore either the Planck constant should be rather large or one should have a non-ohmic quantum counterpart of a direct current in the case of ions and perhaps also protons in the case of neuronal membrane: electronic and perhaps also protonic currents could be still Josephson currents. This would conform to the low dissipation rate.  For this reason, cells evolved to be non-equilibrium dissipative structures.

Enough with the fancy science stuff written to satisfy my future critics who’ll read this.

Let’s get to the Rock star in this story, Robert O. Becker.

The notion of tissues containing a direct current is indeed familiar already from the work of Robert Becker and in the following the results related to laser-induced healing, acupuncture, and DC currents are discussed first. The obvious question is whether these direct currents are actually currents and whether they could be universal in living matter. The mitochondriac model for quantal direct currents is proposed and its possible implications for the model of nerve pulse are discussed. Whether the model is consistent with the vacuum extremal property remains an open question.

Below is Becker’s work in cartoon form on bone semiconduction.

The gist of Becker’s idea on regeneration & wound healing is present below. in that picture represent the state of Becker’s work in 1972.  The implication here is thus:  The DC electric current from the circulatory system loaded with RBC filled with porphyphrins that absorb sunlight and charge up their cells powerfully because they are DEVOID of mitochondria. This charge density increases the Coulomb force and this creates an electric charge density that can be used and transform the matter in an RBC (hemoglobin semiconductive dye) into more primitive cells.

We call this de-differentiation in biology today.  This is evidence of time reversal in a biological system.  Beckers’s work shows us time can be reversed and light energy can be used to do to regenerate brand-new tissues.  This ability remains in humans but it is not as great as it is in the simpler system of the salamander. Nonetheless, his work is eye-opening when you marry it to the idea of Dr. Doug Wallace who says that mitochondrial redox power makes diseases show up and disappear out of the blue as redox varies.  So it raises the question for the mitochondriac how does this happen in us precisely?

I believe the answer is ferroelectricity.

Electro-optics are part of non-linear optical communication and ferroelectricity is part of the electro-optical story in solid-state physics.

NON-LINEAR OPTICS is the base communication system inside of cells. Color = frequency in light.  Nonlinear optics allows us to change the color of a light beam, to change its shape in space and time, and to create the shortest events ever made by humans. It also allows us to turn light into an electric current.  Nature has been at this game a lot longer than Silicon Valley.  They just began the game in 1961.

Many people forget hemoglobin in an RBC is a crystal.  They really forget that when sunlight hits the water in the circulatory system it takes on a physical state change.  Water become liquid crystalline as well = which gains coherent domains which become redox piles of electrons to be moved in the cell system.  Those electrons are critical for ferroelectric coupling in the circulatory system for arterial elasticity and cardiovascular health.

Applying a voltage to a crystal changes the refractive indices of the crystal and introduces birefringence to the system. This is what a mitochondrion does inside human cells.  Light is capable of changing charges and charges change voltages. We change the voltages on our inner mitochondrial membrane and this changes the colors a mitochondrion can emit.  All those colors stimulate different chromophores inside the structure of a mitochondrion to run the metabolism of oxidative phosphorylation and create water, CO2, and heat to reverse the process of photosynthesis.  The light show cephalopods are putting on is the optical representation of their metabolism in real-time.  It doubles as a communication skill because they can vary their metabolism in the compartments of their cells.  They emit these colors to communicate.  It replaces their ability to speak. Humans have had  560 million years to upgrade and change their communication skills.

I told Dr. Huberman I liked cephalopods because as a neurosurgeon they allow me to look back and see the earliest organizations of a neural network.  Many people do not know that Cephalopods evolved during the Cambrian period (∼530 Ma) very close to when this UV expansion fell to Earth.  This also explains how we went from bacteria and archaea so fast into very complex cephalopod animals.  The earliest melanin chemicals were critical to this rapid evolution.   These animals came from a monoplacophoran-like mollusk in which the conical, external shell was modified into a chambered buoyancy apparatus. During the mid-Palaeozoic (∼416 Ma) cephalopods diverged into nautiloids and the presently dominant coleoids.

The strong linear coupling of the director ň to electric field E in ferroelectric liquid crystals can be utilized to perform high-speed electro-optic switching suitable for device applications.

REGENERATION AND THE DC ELECTRIC CURRENT

Beckers’s work is largely unknown and was buried by the military and Big Pharma.

The implication of his work was toward the idea of human regeneration and renovaBeckers’stion of all disease states.  My work is taking up where he left off.  He is an unknown giant in decentralized medicine in my opinion.

His best work was done in bone regeneration which in human remains.  We do not heal fractures, we regenerate the bone completely.  This statement is huge.

The distinction between bone response to stress and to fracture lies in cellular changes which seem to be of great importance. In the case of fracture repair, Becker found that certain cells under appropriate electrical stimulation (direct current in p.p.amp.ranges) would undergo reversion to a more primitive cell type in the human cell line. Becker found that the physical characteristics of the current were KEY in performing this task.

RBCs from the human circulatory system de-differentiated, and this RBC became transformed into a primitive material found in cells and it was subsequently re-differentiated into those cell types needed for the particular tissue repair process required. Becker was able to study some of the electrical parameters of importance in the injury current; the most outstanding was that the effective levels of voltage and current had both upper and lower limits. In other words, voltages or currents above an upper limit were non-productive of cellular changes until cur- rent densities became high enough to produce heating effects.  I believe the reason for this is because the current links to the dielectric constant in water making humans have the ideal refractive index to be able to use solar power to regenerate our tissues.

During night and day, our refractive indices change because of human ferroelectric ability in tissues that link all cells into a synctium.  This gives us a dark and light mode of plasma possible.  It mimics what plants can do in photosynthesis in the dark and light reactions (pic below).  Recall from Burr’s work all plants also exhibit a DC electric current when they are injured as well. This tells the mitochondriac mind this is a light-mediated function of all cells.

Life, and, in particular, its amazing diversity spanning more than 21 orders of magnitude in size, is the most complex physical system in the universe. In spite of this, biological systems obey a host of remarkably simple and systematic empirical scaling laws which relate to how organismal features change with size over many orders of magnitude. These include fundamental quantities like metabolic rate (the rate at which energy must be supplied in order to sustain an organism), time scales (such as lifespan and heart rate), and sizes (such as the length of the aorta or height of a tree trunk). It is a remarkable fact that all of these can be expressed as power law relationships with exponents that are simple multiples of 1 (e.g. ~, 3, 3). They appear to be valid for almost all forms of life, whether it be mammalian, avian, reptilian, unicellular, or plant-like. Clearly, the universal character of these “laws” is telling us something important about the way life is organized photonic energy at the electronic and vibrational state of matter in cells and the constraints under which it has evolved.

Becker wrote that he felt he knew why human regeneration was limited to the bone to just bone and fingertips.  He theorized that one reason why mammals cannot achieve many kinds of regenerative growth seen in amphibians is the absence of adequate “electrical factors” at the injury site. Acting on that hypothesis, his laboratory initially undertook a study of limb regeneration in the nocturnal white rat. The theoretical current/voltage requirements were small enough so that we could consider bimetallic electrogenic couplings as a power source; similar devices had been used by Professor Stephen Smith in 1967 to restore some measure of limb regeneration in the frog, an amphibian capable of limb regeneration when in the tadpole stage of development but lack this ability in adulthood.  I’d remind you at this point frog melanopsin & melanin and human melanin are almost identical homologs.  Becker never knew this about the non visual photoreceptors in tissues.

Becker investigated this aspect of Smith’s work and found that Smith’s silver-platinum junctions far exceeded currents approximately five times that injury regeneration required.  Becker resolved the problem by putting carbon resistors between silver and platinum electrodes and encasing the system in silicon.  When I read this as a resident I knew what this meant.  He created his own WBG semiconductor and changed the current using NLO.  I do not believe Becker had any idea that he was changing the frequency of light in the diode to alter the DC current downward.  It was a remarkable feat that he should have won the Nobel Prize but I do not believe any but myself realized what he did.  When I did I realized what cells were doing inside of us all the time.  We were filled with Wide Band Gapped semiconductors that were changing sunlight into VUV-IR-A light endogenously and using that light to heal and regenerate us while using ferroelectricity to create the DC electric current.  I was astounded at his experimental brilliance.

When Becker made these adjustments guess what happened in that nocturnal white rat?  He was able to regenerate all the tissues a rat limb needs to form.  He never regenerated the entire limb but he verified that the tissue created was brand new and not just a healed limb.  Below was his setup in his 1969 papers.

FROM REGENERATION TO CANCER GENERATION

I briefly discussed this with Huberman and Rick and Huberman was completely unaware of what Becker had found.  I explained to him I learned about Becker’s work as a neurosurgery resident in learning about bone healing. It was here I learned bone does not heal it regenerates fully from primitive cells.

The importance of Becker’s observation is two-fold to the mitochondriac. The growth pattern makes it clear that the effect of the electrical energy was to bring about the de-differentiation of a cell population and its subsequent regrowth and re-differentiation, with the expression of multiple genetic pathways (ex., the controlled reading-out, and application of the all-purpose structural information that all cells possess-the process which occurs in its most complete form during the development of an embryo).

As a neurosurgeon, I immediately thought about the cancers I treat and how glioma behave via glioma progression. According to the result of several studies I read back then, the frequencies of brain tumors are of different rates according to countries worldwide.  This hinted to me the light environment was critical because of latitude and zipcode effects.  It also made me realize nnEMF likely was playing a role in this disease.  In addition, these differences were observed among different ethnic groups in the same country.  This told me local light factors had to be altering the injury currents in the brain and this led to tumor de-differentiation.  This was when I coined the term, “you cannot get well in the same environment you got sick in”.  It was because of Becker’s finding I just mentioned.  I learned early in my residency that low-grade gliomas could be lived with for some time but with time they always de-differentiated into more lethal tumor types.  I realized right away there had to be a link between the sun, gliomas, and the DC electric current.  (see pic below)

What was the cause of BRAIN CANCER?  Appropriate mtDNA control of apoptosis is important for normal functioning, and unregulated apoptosis has been linked to a variety of disease states. Excess apoptosis is thought to contribute to neurodegenerative diseases, whereas insufficient apoptosis can lead to diseases such as cancer. When UV light is blocked exogenous or endogenously from cells non visual photoreceptors, insuffiencent apoptosis results and this blocks cell cycle progression. I mentioned this in the Tetragrammaton podcast but I do not think Huberman understood the power of my idea.

As a result the cell cannot be removed from the tissue by the immune system and then it self isolates from its embryonic tissue. This changes its bio-electric signature inside the organ in question. It acts like an injury does. It is a stimulus that demands a response. The difference in cancer is the stimulus is ABSENT. Because surrounding ultraweak endogenous UV light is not present, the cell forces itself to remain vital as a solo entity within its embryologic position and this change in bio-electric stimulus leads to oncogenic transformation genetically. The lack of ultraweka-UV light emission causes the isolated cell to want to migrate to tissues who do contain the healing UV light stimulus needed to generate the bio-electric fingerprint to control its growth. Every tissue has its own bio-electric signature from morphogensis. Consider tissues to unique self identifying bio-electric barcodes that determine morphogenetic migration from its embryonic form. If this signature does not by molecular resonance, the migrating cell will resume growing but it will do it in another tissue that does not have its specific and sensitive bio-electric passport. This becomes a metastatic cancer focus. This is why the presence or absence of a tissues ultraweak UV bio-photon emission from their mitochondria is critical in apoptosis control and cancer prevention. This is counterintuitive to the centralized idea present in cancer medicine today.

IMPLICATIONS?

Cancer basicially are cells isolated from Nature and its ability to turn sunlight into a DC electric current.  That DC electric connection comes form the sun and links all cells to the whole by the regenerative DC electric current that Becker discovered.  When the bioelectric fingerprint isolates the cell from the tissue it is in, it cannot cooperarate coherent quantum mechanically and the cell loses its ability to undergo apoptosis, and it become invisible to the immune system and it reverts to its own survival modes built into using hypoxia and HIF-1.  This causes the hijacking of the genome.  If the cell is fully participatory in the bio electrical community in a tissue no oncogenesis is possible even if the genetic changes are present.  People who think the BRCA mutation is a death sentence from cancer are smooth brainers who deserve what centralized medicine will give them.  Oncogensis requires that cells isolate themselves because their is no surrounding ultraweak UV light to get them through the mitosis juncture of the cell cycle.  They self isolate by closing their borders and removing their gap junctions.  As soon as they do this, the conditions for existence of cancer becomes possible.  The overall bioelectric state controls quantum coherence, and that state offers the ultimate control of the genetic state.  The Genetic state of the cell is immaterial if the redox potential is controlled by Nature.

I had finally explained why cancer begins and why gliomas have a progression. Within the brain white and grey matter tracts have a very self similar bio-electric passport because they all come from neuroectoderm and the bio-electric power was high because of the mitochondrial capacity in neurons. I realized that the sensitiveity of the frequency match of the bioelectric current had to be controlled by the specific voltages in ferroelectric currents in the brain for low grade gliomas to grow slower and GBM to have very different bio-electric passports that lead to massive growth rapidly. Things began to make sense quantum mechanically to me.

 

SUMMARY

Becker’s experimental results produced in response to the level of current used (a total of 1 to 3 mJAamp) were extensive enough to warrant the prediction that similar-level bio-electric currents could have profound clinical implications for human disease.

For me Becker’s work, was unravelingthe the control mechanisms of life.  I just had to make sense of the experimental data he had. The key was realizing the sun being transformed from cathode ray to terrestrial visible light and being captured by membranes filled with DHA that were connected to the TCA cycle. This caused the forward spin rate. When there was a defect in the bio-electric charge of the membranes, the TCA cycle would spin counterclockwise and this transformed the light emission of the endogenous WBG semiconductors. That change changed the bio-electric passport of the cells using the ferroelectric mechanism. This mechanism was how sunlight was transformed to a charge density on a membrane that leads to a measurable DC electric current in all cells.   This creates a UNIQUE bio-electric passport for neuron migration in the developing brain and it creates a unique bio-electric zipcode within the tracts of the CNS. This unifies the how autism and brain cancer are bio-electric diseases.

THE EUREKA MOMENT AT DAVID’S FOOT

At that moment, I believed I could cure many diseases and not just treat them.  I  therefore now believe that low-level electrical currents and potentials, produced either by direct injection or by semiconductive rectification and induction from an electromagnetic field (melanin in us), have the FULL capability of bringing about very major biological effects of a very basic nature.

Immediately I realize how we went from chimp to human.  I realized at the foot of David how every disease should be approached in decentralized fashion.  It was 180 degrees from what I was taught in medical school.

The changes Becker found in his experiments appeared to be based upon perturbations produced in pre-existing biological electronic control systems which regulate very basic life functions. I knew immediately that they had to be wide-band gapped semiconductors because the electronic state of water and photosynthesis was 12.06 eV.  This meant plants had to use soft Xrays to split water into hydrogen, oxygen, and 2 electrons.  I asked myself does nature make mistakes?

I told Huberman that this peculiarity for me was always vexing.  How could cells split water if they needed soft X-rays to do so?  Becker’s work told me cells were solid state.  Then it clicked.  We were filled with WBG semiconductors that took the visible spectrum light in eV and added to it with our cellular design.  Then splitting water was easy.  So I pulled out a chlorophyll molecule and saw Mg sitting inside a nitride cage and I looked up the band gap of MgN.  Problem solved.  Its band gap was over 7 eV.  Becker’s fexperiments explained a lot to my simple brain.  They hold MASSIVE promise for a better understanding of ALL of life’s control systems and for clinical application to many mitochondrial diseases.

Becker is a giant to this decentralized mitochondriac.  I cannot overstate the impact of his work on me. Becker taught me that just understanding biochemistry was the losing hand centralized medicine plays.

From his work, the biological effects involve basic functions of living material that are under remarkably precise control by mechanisms that have, to date, escaped description in terms of solution biochemistry. This suggests that bio-electromagnetic phenomena are fundamental attributes of living things, ones that must have been present in the first living things. The traditional approach to biogenesis postulates that life began in an aqueous environment, with the development of complex molecules and their subsequent sequestration from the environment by membranous structures. The solid-state approach proposes an origin in complex crystalline structures that possess such properties as semi-conductivity, photoconductivity, and piezoelectricity. All of the reported effects of electromagnetic forces seem to lend support to the latter hypothesis.

With this knowledge, I went from a centralized pusher of drugs to a decentralized physician pushing solid state physics in Nature overnight.

The neural electronic system also seemed to be related to levels of consciousness and biological cycles, and Becker’s work developed the thesis that this system furnishes the linkage mechanism between electromagnetic forces in the environment and biological cyclic behavior.  In mammals, I found the electromagnetic induction of melanin from POMC was the key to the human system.  It was on the shoulders of Becker, my ideas have gone further.  Without his insight, I would be like any other centralized MD.   In my opinion, human ferroelectricity in the neural and circulatory systems is another critical link in explaining his experimental findings.  There is not a disease we cannot tackle with this wisdom.

The most amazing thing light has built is my species.  It astounds me that light is slowed down by atoms in cells on Earth in a specific way that creatures like us do.  I am amazed at how creation occurred.

All these thoughts created for you above came from starlight.  Sunlight is our remedy in this life.  I need to understand it fully before my “pilot light” goes out.  Light organizes matter and hides in its electronic state but the type of light, the spectrum of this light from a source, has its own unique ability to sculpt atoms in specific ways to create new things from its inherent organizing ability.  It is this ability hidden deep within the light that is the key to understanding life.  It provides change without the perception of change.  The thing that shows up every morning, which is most familiar, remains the most mysterious force in the Universe.  That force organized every life system and every feeling of love that has ever existed. Matter exists to make love to light, to separate its electric and magnetic fields in ways that we just do not understand, and from this dance, light can sculpt a life, make a child, and create a new species.  Everything man has known comes from the mysterious moves of our star’s light as it fell to this wet rocky planet.  It is sheer amazement to me.

Living systems are nests of abiotic carbon, hydrogen, oxygen, and nitrogen, organized together with traces of a few other elements, yet of a complexity of structure that has hitherto resisted all attempts at complete analysis because we do not understand how light and water bind and weave the process of atoms in things.  This makes our protoplasm the most enduring and the most easily destroyed of substances we know; its molecules are constantly programmed electronically by light to break down constantly, yet reorganize under solar power to furnish the power for the manifestations of many vital phenomena.  Yet, through its remarkable property of assimilation of light, a power possessed by few other things on earth, it constantly builds up its substance anew from the surrounding medium and it avoids our perception of its recipe.

Now I knew how life operated at its fundamental levels. Now you do too! Below is one of my members, who just did not get the ideas in this blog together in her own life. She just died of cancer this week. I dedicate this blog to her.

CITES

1. Becker, R. 0., and D. G. Murray, “The Electric Control System Regulating Fracture Healing in Amphibians,” Clinical Orthopedics and Related Research, Vol. 73, pp. 169-98, 1970.

2. Frost, Harold M. (ed.), Bone Biodynamics. Boston: Little Brown and Co., 1964.

3. Szent-Gyorgyi, Albert, Introduction to a Submolecular Biology. New York: Academic Press, 1960.

4. Becker, Robert O. Technology Review, December 1972

5. My neocortex —-> https://threadreaderapp.com/thread/1780379857295200331.html

6. https://www.youtube.com/watch?v=IKPC64n_U0s&t=4161s

7. Go to the 2:24 and listen until 2:28, the rest is superfluous —-> https://www.youtube.com/watch?v=p3lsYlod5OU&t=8898s

8. Michael Levin’s Website: https://drmichaellevin.org

Do you know humans are broken and moved to action by their master?

What are minerals at their most fundamental level? Atoms. What are they made of? Electrons, protons, and neutrons have their quantum spin, and the angular orbital momentum is changed by light from the sun. Is this transferred to water and things in our cells? Yep. This is how evolution really operates below your level or a Darwinist to sense it

.

 

Why does just 3% of DNA code for proteins? How could it be the be-all-end-all that the neo-Darwinists say it is? What does the other 97% of DNA do? Is the extra DNA that acts like dark matter in us actually an owner’s manual for how light, our master, is transformed into bioelectricity whose job it is to power up and move the chains found in our proteins to move like a wind chime operates to make music? Is bio-electric function vital to understanding how our master controls the dark matter in us to allow life to manifest somehow, and is centralized science missing?

DNA only codes for proteins. Protein structure is the three-dimensional arrangement of atoms in a molecule. Proteins are polymers of specifically polypeptides formed from sequences of amino acids that the linear DNA code provides. The code of DNA, however, has many other electronic codes contained within it. Watson and Crick did not understand this in 1953, and many in centralized biology are still stuck on their old ideas. Modern decentralized epigenetics and transposons are tuned and turned on and off by bioelectrical signals transformed from sunlight, which have shown us that Watson and Crick’s ideas about DNA are outdated. This implies that the DNA code and proteins it makes are clues to a “quantum evolution” at the depths of life deep inside your cells.

The design process of life begins with the DNA code. Biology today is a detailed, disorganized collection of disparate facts. It is like a hoarder’s basement or a rat’s nest. There is no design connecting to what is buried in DNA’s code. You can scoop up a bag full of facts and try to make sense of it, but that would be an exercise in futility. Proper biological knowledge is fractal and non-linear, filled with optical magics thrown in the recipe.

The design can be complex, with microscopic details, but the overall design is coherent and beautiful. It would help if you linked them together electrically to make extensive collections of proteins act as one and become coherent. This idea implies that they must be tuned as a wind chime is. Cells should have some bioelectric tuning ability built into their protein structure. Do you see what I see yet?

VIDEO

Just one violin that is out of tune in an orchestra or one voice that is off-key in a choir will ruin a beautiful harmony or an enchanting ensemble. It matters not how loudly or softly it grates; if it does not stop, the performance will end.

So it is with the cells of our bodies and of the birds, insects, animals, and plants whose music fills the Earth. When a jarring note is introduced, no matter how softly, chords become discords, melody becomes noise, life degrades and disappears, and chronic disease epidemics become commonplace.

Life, Information, and Electricity

The cohesion of life does not come from chemistry. It comes from the Earth, Sun, and stars.

K.H. Li wrote, in his forward to the book Electromagnetic Bio-Information:

“The informational aspect of biological systems characterizes the essential view of life. And this is less reflected by biochemical findings, but rather by a level beyond the domain of chemical reactivity, namely that of electromagnetic fields.” [1]

Nikolai Kositsky, Aljona Nizhelska, and Grigory Ponezha reviewed 40 years of research in Ukraine and Russia and concluded:

“Biological effects [of electromagnetic radiation] depend not on the strength of the energy carried into one or another system, but on the information carried into it.” [2]

W. Grundler and F. Kaiser wrote:

“Living cells exhibit a high degree of information processing and communication… It is clearly demonstrated that a fast oscillating, very weak outer field is influencing the biological reactions of cells… We have to take into account an ‘internal’ oscillator (the cell itself or parts of the cell or of its environment) coupling with the outer field.” [3]

John Zimmerman and Vernon Rogers wrote:

“Electromagnetic bioinformation depends on the ability of organisms to emit, receive, and interpret spatiotemporal patterns of electromagnetic fields.” [4]

Herbert L. König, a student of Winfried Schumann, wrote:

“Electromagnetic forces in general must play a role of an as yet incalculable importance in the information transfer between or to living organisms.” [5]

Ulrich Warnke wrote:

“The communicative form of antennae contact in bees and ants can be registered by an oscillograph. Every time a short contact occurs between the antennae, a signal is generated in the recipient’s electrolyte system in the form of an impulse.” [6]

Günther Becker showed that termites’ gallery building rate was affected by termites’ existence in an adjoining container but not if the wall between them was shielded with a conductive material. “These results indicate that communication among termite groups is based on either electric or electromagnetic fields produced by the insects,” he wrote. [7]

Bernhard Ruth wrote that the growth of plants and animals cannot be explained in terms of chemical reactions because “all chemical reactions occur equally in all directions,” and biological growth is directional. “The existing cells of an organism have to determine when and where a new cell is to be generated by mitosis. This can only be achieved by means of an information transfer which stimulates the required cell to divide, and which is not emitted in all directions homogenously.” [8]

Helmut A. Fischer wrote:

“There is good reason for believing that, in addition to mechanical and chemical forms of communication, there are more biophysical ways of communication… The findings made so far confirm that the biochemical processes in a cell, besides thermic effects, also elicit other electromagnetic signals.” [9]

Igor Jerman wrote:

.

“Coherent electromagnetic oscillations in cells permit ordered intermolecular processes and highly selective attractions between enzymes and substrates. These oscillations… represent an important means of intercellular long-range connection and thus have an important role in maintaining an intercellular order… Neoplasms follow from the fact that some of the cells within the organism escape from the intercellular coherent field and thus from the intercellular order.” [10]

Living cells emit signals throughout the electromagnetic spectrum

In their study, “Electromagnetic emission at micron wavelengths from active nerves,” Allan Fraser and Allan Frey measured infrared emissions from nerves with wavelengths between 2 and 20 microns at a strength of 6 μW/cm2. [11]

Bernhard Ruth detected light photons emitted by plants:

“The light intensity emitted by seedlings of wheat, beans, lentils, and corn varied between 700 cps (counts per second) and 250 cps… The spectral distribution extended from 400 nm to 600 nm… Yeast cells show a radiation of between 150 and 380 nm.” [8]

Shou Sin-Sung wrote that “DNA is a possible radiation source.” [12]

A.H. Jafary-Asl and Cyril W. Smith detected radio frequency signals from yeast at a frequency of 8 MHz. [13]

Herbert A. Pohl detected signals at 7 and 33 kHz from a species of algae. [14]

J. Kent Pollock and Douglas G. Pohl, in dielectrophoresis studies, detected RF emissions from mouse cells at frequencies between 4 and 9 MHz. Similar emissions were detected from cells of bacteria, yeast, worms, chickens, frogs, monkeys, and humans. Maximum emissions occurred during cell division, and no emissions from dead cells:

“The evidence from the m-DEP experiments and from the closely related pattern experiments consistently indicate that cells are producing radio frequency electric fields.” [15]

Sergey Sit’ko and his colleagues measured emissions from the human body between 37-78 GHz at 0.000000000000001 to 0.0000000000000001 μW/cm2Hz. [16]

It takes little or no power to interfere with life

Allan Frey wrote:

“Electromagnetic fields are not a foreign substance to living beings like lead or cyanide. With foreign substances, the greater the dose, the greater the effect — a dose-response relationship. Rather, living beings are electrochemical systems that use very low frequency EMFs in everything from protein folding through cellular communication to nervous system function. To model how EMFs affect living beings, one might compare them to the radio we use to listen to music.

“The EMF signal the radio detects and transduces into the sound of music is almost unmeasurably weak. At the same time, there are, in total, strong EMFs impinging on the radio. We don’t notice the stronger EMF signals because they are not the appropriate frequency or modulation. Thus, they don’t disturb the music we hear. However, if you impose an appropriately tuned EMF or harmonic on the radio, even if it is very weak, it will interfere with the music. Similarly, if you impose a very weak EMF signal on a living being, it has the possibility of interfering with normal function if it is properly tuned. That is the model that much biological data and theory tell us to use, not a toxicological model.” [17]

Gerard Hyland said:

“The human body is an electrochemical instrument of exquisite sensitivity.” [18] “If a signal can operate a mechanical device, it can disturb every cell in the human body.” [19]

Igor Belyaev wrote:

“While the dose rate/SAR concept is adequate for description of acute thermal effects, it is not applicable for chronic exposures to N[on]T[hermal] M[icro]W[aves].” [20] and ”The 51.755 GHz resonance frequency of the cell reaction to MMWs did not depend on power density (PD) in the range from 10(exp-19) to 3 × 10(exp-3) W/cm2.” [21]

Ross Adey, at Loma Linda University, wrote:

“We have discovered some of the keys to understanding how body cells ‘whisper’ to one another, and, in so doing, we have discovered some of the keys to understanding how electromagnetic fields, so weak that some scientists have regarded them as incapable of biological effects, are detected by living tissues, and we have studied some of the likely consequences for human health… These fields can exert effects even at intensities near zero; in other words, a lower limit or threshold may not exist.” [22]

Neil Cherry presented “conclusive evidence” that “the safe level of exposure is zero” [23] and that radio signals “can interfere with hearts, brains and cells at extremely low intensities.” [24]

Dr. Robert O. Becker wrote:

“There is no effective way to shield yourself from environmental fields except to avoid areas where they are prevalent” [25] and “If the system’s sensitivity is as presently described, then frequency becomes a more important parameter in any experiment than field strength.” [26]

In The Body Electric, he wrote:

“The accumulated research has clearly shown that small doses often have the same effects as larger ones… Indeed there has already been one report of brain wave changes suggesting resonance of neural electrical currents with radio waves and microwaves down to a billionth of a microwatt… We must understand that no amount of artificial EMR, no matter how small, has been proven safe for continuous exposure. Bioeffects have been found at the lowest measurable doses.” [27]

Herbert L. König wrote:

“Biological systems have sensitivity values of the same order of magnitude as the field intensity values of natural fields.” [5]

William Bise testified before the U.S. Senate about the effects on brain waves that he elicited by radio waves at near-zero intensity. The results of his experiments ought to terrify every person who ever uses a cell phone and every doctor who is confronted with the extraordinary amount of anxiety and depression in his or her patients today because the radiation in Bise’s experiments, at exposure levels 10,000,000,000 to 100,000,000,000,000 times lower than a cell phone, had strong and instantaneous effects on all subjects’ brain waves and mental states:

“A pilot study was conducted on five men and five women volunteers… They ranged in age from 18 to 48 years. Three had been occupationally exposed to RF energy; the other seven had not, and all were in apparent good health. The RF ranges covered from .1 to 960 Mhz C[ontinuous] W[ave] and 8.5 to 9.6 Ghz pulse modulated. Power levels were varied from 10(exp-16) wt/cm2 to 10(exp-12) wt/cm2… The experimental time for each volunteer was typically 50 minutes…

“Subjects’ EEG traces displayed desynchronized alpha waves of 15 to 25 percent higher than normal amplitude, and slow waves appeared at certain radio frequencies. Conversely, diminution and desynchronization of alpha wave amplitude on the 20 to 50 percent order occurred at other radio frequencies, and 2 to 6 Hz slow waves appeared. These two anomalous patterns were found in both men and women volunteers. Mental attitudes appeared to change during the tests. CW frequencies at a power density of about 10(exp-15) wt/cm2, which produced EEG changes in males, were found between 130 and 780 Mhz. Female volunteers’ EEG alterations occurred between 350 and 960 Mhz. Pulse modulation tests on two males, at a power density of about 10(exp-12) wt/cm2, showed EEG changes around 9.1 and 9.15 GHz. Brain waves changed almost immediately upon tuning a generator to a frequency that produced them and then reverted to their normal patterns when the generator frequency was altered or turned off.” [28] Read Marino’s book “Going Somewhere for more astounding facts you and your doctor are ignorant of.

Sheldon Meyers, Director of the U.S. Environmental Protection Agency’s Office of Radiation Programs, told Congress that “it is not possible to assign a low-intensity limit or threshold below which the exposures are without effect.” [29]

Reba Goodman and Martin Blank wrote:

“Induction of the stress response by magnetic fields occurs at 14 orders of magnitude lower energy density than with thermal stimuli, the current benchmark for cell phone safety standards.” [30]

Yury Shckorbatov found evidence of cell damage after only one second of exposure to 18.75 GHz microwaves at a level of 0.2 mW/cm2. [31]

Low power can be more harmful than high power.

Andrew Wood, Rohan Mate, and Ken Karipidis reviewed 107 experimental studies and found that a lower exposure level tended to have a greater biological effect, and the difference was highly significant (p < 0.001). [32]

Stefano Cucurachi et al. reviewed 113 peer-reviewed field and laboratory studies and found that RF radiation with the lowest power tended to cause the most significant ecological damage. [33]

Maria Sadchikova found that among people occupationally exposed to RF radiation in the 1950s, 1960s, and 1970s, the sickest were those exposed to the lowest, not the highest, levels. [34], [35]

Abraham Lilienfeld analyzed the health of Moscow embassy employees during the 1950s, 1960s and 1970s, when Russia was continuously irradiating the embassy with microwaves. His report was written for the U.S. Department of State. Table 6.32 of his report shows that male employees exposed to the lowest level of radiation had the most symptoms in 18 of 20 symptom categories. [36]

They had more:

depression

migraine

lassitude

irritability

nervous disorders

anxiety

vibrations

intraocular pain

sensations

loss of appetite

difficulty concentrating

memory loss

dizziness

finger tremor

hallucinations

insomnia

neurosis

other symptoms

Liliya M. Fatkhoutdinova studied the effects of video display terminals on blood pressure. Lower levels of electromagnetic fields raised blood pressure more than higher levels. [37]

Vladimir N. Binhi and Robert J. Goldman studied the proliferation of wound cells in response to electric fields. They wrote:

“Most dramatic is that relatively intense electric fields sometimes do not cause appreciable effect while smaller fields do.” [38]

Herbert L. König wrote:

“Exceptionally intense fields often cause no reaction at all.” [5]

Leif Salford, Bertil Persson, Arne Brun, Henrietta Nittby and their team at Lund University in Sweden researched the effects of RF radiation on the blood-brain barrier for 20 years. They found that the lowest levels of exposure caused the most damage to the blood-brain barrier. [39] They calculated that you will do more damage to your brain if you hold a cell phone one meter away from you than if you hold it up to your head. [40]

Dimitris Panagopoulos found that RF radiation reduced reproduction in fruit flies. The maximum impact on fruit fly reproduction occurred when the source of radiation was at some distance away from the flies. [41]

Igor Belyaev, experimenting on E. coli, found that genetic effects occurred at specific frequencies and that the magnitude of the effect did not change with power level over 16 orders of magnitude, all the way down to 0.000000000001 μW/cm2. [21]

Numerous scientists in many laboratories — Carl Blackman et al. at the U.S. Environmental Protection Agency [42]; Suzanne M. Bawin, Leonard K. Kaczmarek and W. Ross Adey [43]; Sisir K. Dutta et al. [44]; Jean-Louis Schwartz, Dennis E. House and Geoffrey A. R. Mealing [45]; and Kumud K. Kunjilwar and Jitendra Behari [46] — found that calcium depletion from brain and heart cells occurred at specific frequencies and exposure levels and did not increase with power. Dutta found a 3,000-fold decrease in power caused a 4-fold increase in calcium exiting from cells.

W. Grundler and F. Kaiser halved the growth rate of yeast at a precise microwave frequency. The magnitude of the effect of this frequency did not change with intensity over several orders of magnitude, down to 5 pW/cm2. [3]

Cooking Your Brain and Your DNA

Here are some other findings that should terrify anyone who uses a cell phone, considering the unprecedented numbers of young people today with cancers and neurological diseases.

First are some measurements made by Markus Antonietti, Director of the Max Planck Institute of Colloids and Interfaces in Germany. In 2006, when cell phone use was becoming universal, he wondered what they might be doing to the brain. Cell phones exposed the brain to about 1 W/kg SAR, which did not heat the whole brain by more than one degree Celsius, but what about the conditions that exist in the tiny synapses, the junctions between neurons where nerve impulses are transmitted from one nerve cell to another? His research team decided to simulate the conditions between cell membranes with tiny fat droplets in salt water. [47] “Ions accumulate on these,” reported Zeit Online, the newspaper that interviewed him, “and by changing the salt concentration and the droplet size, the conditions of biological tissue can be simulated, i.e., a kind of concentrated liquid brain.

“‘And now comes the tragedy,’ said the Max Planck Director. ‘Exactly where we are closest to the conditions in the brain, we see the strongest heating.’ Temperature peaks of 100 degrees. He had expected to warm, but not to this extent. ‘There is a hundred times as much energy absorbed as previously thought. That is a horror.’” [48]

It turns out a cell phone not only boils your synapses but also your DNA. A number of research teams have discovered that DNA is a good conductor and so, as in the synapses, RF radiation is conducted and amplified tremendously in DNA.

Jacqueline K. Barton and her colleagues at the California Institute of Technology in Pasadena observed ultrafast electron transfer in DNA over large distances. [49] “In effect,” she told Science News, “DNA acts like a molecular wire.” [50]

Hans-Werner Fink and Christian Schönenberger reported that the conductivity of DNA is 105 Siemens per meter, which is ten times larger than that of most electrically conducting polymers and about one-tenth the conductivity of mercury. [51]

Charles Polk tells us what the consequences of this are. Based on Fink and Schönenberger’s measurements, Polk calculated that the rate of temperature increase in the interior of DNA exposed to a cell phone at 1 W/kg SAR is 60 degrees Celsius per second! [52].

Your cell phone, if you still use one, is cooking your brain and damaging it, during every second that you use it. The cell towers that it commands are sickening us, no matter how far away from one we manage to be. The satellites — 9,500 of them and increasing rapidly — are polluting our bodies, sterilizing our planet, and severing our connection to our sources of vitality beneath our feet, in the air, in the oceans, and in the heavens.

In my constitutional amendment, there is an entire section dedicated to nnEMF protection that will begin in El Salvador. It not only protects patients but it also has specifics in it for clinicians, students, teachers, and schools. The world is changing right around you now.

Do you sense it yet? If not, why not? Might it be the nnEMF you are imbibing?

CITES

[1] K.H. Li. Foreword to Electromagnetic Bio-Information, Fritz Albert Popp et al., eds., Urban & Schwarzenberg, München (1989).

[2] Nikolai Kositsky, Alona Nizhelska, and Grigory Ponezha. Influence of High-frequency Electromagnetic Radiation at Non-thermal Intensities on the Human Body. No Place To Hide 3(1) Supplement (2001).

[3] W. Grundler and F. Kaiser. Experimental evidence for coherent excitations correlated with cell growth.” Nanobiology 1:163-176 (1992).

[4] John Zimmerman and Vernon Rogers. Biomagnetic Fields as External Evidence of Electromagnetic Bioinformation. In Electromagnetic Bio-Information, Fritz Albert Popp et al., eds., 1989, pp. 226-237.

[5] Herbert L. König. Bioinformation – Electrophysical Aspects. In Electromagnetic Bio-Information. Proceedings of the Symposium, Marburg, September 5, 1977, Fritz Albert Popp et al., eds. Urban and Schwarzenberg, München 1979, pp. 25-54.

[6] Ulrich Warnke. Information Transmission by Means of Electrical Biofields. In Electromagnetic Bio-Information, Fritz Albert Popp et al., eds., 1979, pp. 55-79.

[7] Günther Becker. Communication between Termites by Means of Biofields and the Influence of Magnetic and Electric Fields on Termites. In Electromagnetic Bio-Information, Fritz Albert Popp et al., eds., 1979, pp. 95-106.

[8] Bernhard Ruth. Experimental Investigations on Ultraweak Photon Emission. In Electromagnetic Bio-Information, Fritz Albert Popp et al., eds., 1979, pp. 107-121.

[9] Helmut A. Fischer. Photons as Transmitter for Intra- and Intercellular Biological and Biochemical Communication – The Construction of a Hypothesis. In Electromagnetic Bio-Information, Fritz Albert Popp et al., eds., 1979, pp. 175-180.

[10] Igor Jerman. Electromagnetic Origin of Life. Electro- and Magnetobiology 17(3): 401-413 (1998)

[11] Allan Fraser and Allan H. Frey. Electromagnetic emission at micron wavelengths from active nerves. Biophysical Journal 8: 731-734 (1968).

[12] Shou Sin-Sung. A Possible Biophotochemical Mechanism for Cell Communication. In Electromagnetic Bio-Information, Fritz Albert Popp et al., eds., 1979, pp. 151-174.

[13] A.H. Jafary-Asl AH and Cyril W. Smith. Biological dielectric in electric and magnetic fields. IEEE Annual Report Conference on Electrical Insulation and Dielectric Phenomena, 1983, p. 350.

[14] H.A. Pohl. AC field effects of and by living cells. In Chiabrera A. et al., eds., Interactions between electromagnetic fields and cells, NATO ASI Series A, Life Sciences, Plenum, NY (1985), pp. 435-456.

[15] J. Kent Pollock and Douglas G. Pohl. Emission of radiation by active cells. In Biological Coherence and Response to External Stimuli, Herbert Fröhlich, ed., Springer Verlag, Berlin, 1988, pp. 139-147.

[16] Sergei P. Sit’ko, Yurij A. Skripnik and Aleksey F. Yanenko. Experimental Study of Mm-Range Radiation from Certain Objects. Physics of the Alive 6(1): 15-18 (1998).

[17] Allan H. Frey. Is a toxicology model appropriate as a guide for biological research with electromagnetic fields? Journal of Bioelectricity 9(2):233-234 (1990).

[18] Gerard J. Hyland. Physics and biology of mobile telephony. The Lancet 356:1833-1836 (2000).

[19] Personal communication, December 2018.

[20] Igor Y. Belyaev. Duration of Exposure and Dose in Assessing Nonthermal Biological Effects of Microwaves. In Dosimetry in Bioelectromagnetics, CRC Press 2017, pp. 171-184.

[21] Igor Y. Belyaev et al. Resonance effect of millimeter waves in the power range from 10–19 to 3 x 10–3 W/cm2 on Escherichia coli cells at different concentrations. Bioelectromagnetics 17: 312-321 (1996).

[22] W. Ross Adey. Testimony before the Ad Hoc Subcommittee on Consumer and Environmental Issues of the Committee on Governmental Affairs, United States Senate, August 10, 1992.

[23] Neil Cherry. Evidence of brain cancer from occupational exposure to pulsed microwaves from a police radar. Lincoln University, August 15, 2001.

[24] Neil Cherry. Safe Exposure Levels. Lincoln University, April 25, 2000.

[25} Robert O. Becker. Personal communication, May 15, 1986.

[26] Robert O. Becker. A theory of the interaction between DC and ELF electromagnetic fields and living organisms. Journal of Bioelectricity 4(1):133-140 (1985).

[27] Robert O. Becker and Gary Selden. The Body Electric: Electromagnetism and the Foundation of Life, NY: William Morrow 1985, pp. 312-313.

[28] William Bise. Hearings before the Committee on Commerce, Science, and Transportation, United States Senate, Ninety-Fifth Congress. First Session on Oversight of Radiation Health and Safety, June 16, 17, 27, 28, and 29, 1977, Serial No. 95-49, pp. 1220-1223.

[29] Sheldon Meyers. Oversight Hearing before the Subcommittee on Water and Power Resources of the Committee on Interior and Insular Affairs, House of Representatives, First Session on Health Effects of Transmission Lines, October 6, 1987, Serial No. 100-22, p. 166.

[30] Reba Goodman and Martin Blank. Magnetic field-induced stress responses in biological cells by use of cell phones. EBEA 2001. 5th International Congress of the European BioElectromagnetics Association (EBEA). 6-8 September 2001, Helsinki, Finland. Proceedings, pp. 197-198.

[31] Yury G. Shckorbatov et al., Modification of electrokinetic properties of nuclei and membrane permeability in human buccal epithelial cells under the influence of low-level microwave radiation. EBEA 2001, pp. 204-206.

[32] Andrew Wood, Rohan Mate, and Ken Karipidis. Meta-analysis of in vitro and in vivo studies of the biological effects of low-level millimeter waves. Journal of Exposure Science & Environmental Epidemiology 31: 606–613 (2021).

[33] Stefano Cucurachi et al. A review of the ecological effects of radiofrequency electromagnetic fields (RF-EMF). Environment International 51: 116-140 (2013), Table 4.

[34] Maria N. Sadchikova. State of the nervous system under the influence of UHF. In The Biological Action of Ultrahigh Frequencies, A. A. Letavet and Z. V. Gordon, eds., Academy of Medical Sciences, Moscow, 1960, pp. 25-29.

[35] Maria N. Sadchikova. Clinical manifestations of reactions to microwave irradiation in various occupational groups. In Biologic Effects and Health Hazards of Microwave Radiation: Proceedings of an International Symposium, Warsaw, 15-18 October 1973, P. Czerski et al., eds., 1974, pp. 261-267.

[36] Abraham Lilienfeld. Evaluation of Health Status of Foreign Service and Other Employees from Selected Eastern European Posts. Johns Hopkins University, Department of Epidemiology, Baltimore, MD, prepared for Dept. of State, DC Office of Medical Services, U.S. Dept. of Commerce, National Technical Information Service, July 31, 1978.

[37] Liliya M. Fatkhoutdinova. Hemodynamic indices in VDT users with different exposure to electric and magnetic fields and controls,” EBEA 2001, pp. 292-294.

[38] Vladimir N. Binhi and Robert J. Goldman. The Ion Interference and Electric Field-Induced Wound-Cell Proliferation. In BEMS Twenty-Second Annual Meeting in Cooperation with the European Bioelectromagnetics Association, Abstract Book. The Technical University, Munich, Germany, June 11-16, 2000, pp. 11-12.

[39] Bertil Persson, Leif Salford, and Arne Brun. Blood-brain barrier permeability in rats exposed to electromagnetic fields used in wireless communications. Wireless Networks 3:455-461 (1997).

[40] Henrietta Nittby, Gustav Grafström, Jacob L. Eberhardt et al. Radiofrequency and Extremely Low-Frequency Electromagnetic Field Effects on the Blood-Brain Barrier. Electromagnetic Biology and Medicine 27: 103-126 (2008).

[41] Dimitris J. Panagopoulos. Analyzing the health impacts of modern telecommunications microwaves. In L. V. Berhardt, ed., Advances in Medicine and Biology, vol. 17, Nova Science Publishers 2011, chapter 1.

[42] Carl F. Blackman et al. Induction of calcium-ion efflux from brain tissue by radiofrequency radiation. Bioelectromagnetics 1:35-43 (1980).

[43] Suzanne M. Bawin, Leonard K. Kaczmarek and W. Ross Adey. Effects of modulated VHF fields on the central nervous system. Annals of the New York Academy of Sciences 247: 74-80 (1970).

[44] Sisir K. Dutta et al. Microwave radiation-induced calcium ion flux from human neuroblastoma cells: dependence on depth of amplitude modulation and exposure time. In Biological Effects of Electropollution, Sisir K. Dutta and Richard M. Millis, eds. Information Ventures, Phila., 1986, pp. 63-69.

[45] Jean-Louis Schwartz, Dennis E. House, and Geoffrey A. R. Mealing. Exposure of frog hearts to CW or amplitude-modulated VHF fields: selective efflux of calcium ions at 16 Hz. Bioelectromagnetics 11: 349-358 (1990).

[46] Kumud K. Kunjilwar and Jitendra Behari. Effect of amplitude-modulated RF radiation on cholinergic system of developing rats. Brain Research 601:321-324 (1993).

[47] Christian Holtze, R. Sivaramakrishnan, Markus Antonietti, et al. The microwave absorption of emulsions containing aqueous micro- and nanodroplets: A means to optimize microwave heating. Journal of Colloid and Interface Science 302: 651–657 (2006).

[48] Quoted by Max Rauner in Zeit Online, August 21, 2006.

[49] Chaozhi Wan et al. Femtosecond dynamics of DNA-mediated electron transfer. PNAS 96 (11) 6014-6019 (1999).

[50] Corinna Wu. An Electrifying DNA Debate: New evidence explains how DNA conducts charge,” Science News 156(7): 104-106 (1999).

[51] Hans-Werner Fink and Christian Schönenberger. Electrical conduction through DNA molecules. Nature 398: 407-410 (1999).

[52] Charles Polk. Implications of Measured Electrical Conductivity of DNA for Bio-Effects of E.M. Fields. In BEMS Twenty-Second Annual Meeting, 2000, pp. 22-23.

The biggest fallacy we are going to test in El Salvador is the one that functional medicine sells to the public. They believe that ordering “their labs” leads to more functional changes that actually happen in cells to change outcomes in disease.

They got this idea from centralized medical textbooks of biochemistry. They knew allopathic docs order certain labs, so they tried to be slick and order more esoteric labs that might better explain organ function. What they forget is this idea is a very reductionist way of doing scince.

What might they have missed from the decentralized perspective? Their heads are filled with beautiful diagrams to illustrate a falsehood belief that biomolecules are static actors who dance in ‘lock and key’ fashion. Centralized biologists/biochemists currently believe in this static principle of ‘recognition’ between enzymes and their respective substrates even today. They think this exists between signal molecules and their respective receptor proteins, as well as between different species of proteins. Yet, everything in quantum theory tells us that molecules never stand still, they always move and vibrate. How would a vibrating lock and key ever work? Moreover, the most important biomolecules, proteins are no exception to this vibration rule. Indeed, the most mobile proteins are enzymes which generally have great specificities for their substrates, and the most mobile parts of the antibody molecules are precisely those containing the recognition sites for corresponding antigens. These observations of reality are difficult to reconcile with the lock and key model. What is more likely to be responsible for intermolecular complexes in the cellular organization is the universal electromagnetic attractive forces between molecules.

The biggest problem for functional medicine, in my opinion? THE STORAGE OF ENERGY tells us labs are useless because most energy in the living state is sotred at the electronic level in cells. Do labs measure this level? NOPE. Since we know this is true today because of quantum biological experimentation, we should be forced back to the drawing board and start rethinking about the theorem of Prigogene and dissipative structures. shouldn’t we? Is functional medicine doing this? Nope?

This is why they will not get a pass in El Salvador. We will test their beliefs before we rubber stamp their beliefs in our system. Nockchains will help us execute this task via my decentralized loop in the Constitutional Amendment.

Sunlight creates electric fields in our atmosphere every day and that sunlight creates a Coulomb force in our body. Coulomb force is an electrostatic force. Electrostatic phenomena arise from the forces that electric charges exert on each other. Such forces are described by Coulomb’s law. Even though electrostatically induced forces seem to be rather weak because of how we experience them in life, when the scale shrinks, as it does in a cell, the electrostatic force increases tremendously in strength as the scale drops. For example, some electrostatic forces such as the one between an electron and a proton, that together make up a hydrogen atom, are about 36 orders of magnitude stronger than the gravitational force acting between them. The electrostatic force generated in your skin is another example of a strong electrostatic force because the skin, as an insulator can hold large amounts of charge. Here is a reminder for all functional practitioners thinking of opening a conceirge practice in El Salvador:

Cellular organization is the key to precision optical signaling. Life is all about optimizing AMO physics INSIDE OF CELLS. It transforms energy from the environment to do this. Modern physics now has proven that energy and information are equivalent in physics. Landauer’s Principle of 1961 & Shannon’s 1948 work was critical in making this linkage.

Modern quantum biology has experimentally proven that energy is trapped directly at the electronic level in cells. Energy is stored not only as vibrational and electronic bond energies in biochemicals, but also in the structure of the system: its membranes, and in gradients, fields and flow patterns, compartments, organelles, cell water, and tissues. All this in turn enables organisms to mobilize their energies coherently at any time it is needed and hence make available the entire spectrum of stored energies for physiological work. It is energy on demand by atomic design. Now explain to me how your labs are going to solve a patient’s mitochondrial problem?

This is not written as a warning to you. It is written as a promise to the public that we will protect your health from pseudoscience.

Since 1998, the water at Lake Coatepeeque has been tested via labs and has not shown the real reason the water changes color as it does now. The belief is that the algae do it, but the tests are not conclusive. The reason they are not conclusive is covered in this blog. The water in this caldera sits on top of a huge magma chamber that is transfering energy to the water in the caldera and this leads to phase transition of the hydrogen bonding network in water.

If you cannot explain it, you do not know the cause.

The same idea is why we will be holding feet to the fire when you practice your version of centrlaized science. If your patients do not get consistent results from your excessive testing, and you cannot explain why to your PEERS, you likely won’t be practicing your craft here without some risk to your portfolio.

You’ve been warned.

CITES

New podcast out today: In this podcast I talk about chronic diseases and how we are going to deal with this at the 13N latitude. Many of these idea have been shared with Nayib bukele, Nicole Shanahan, and Bobby Kennedy Jr https://www.thehighersidechats.com/dr-jack-kruse-light-water-magnetism-the-sacred-cows-of-health/

https://www.youtube.com/watch?v=b7iuFIKmkN4

THEORY OF CONSCIOUSNESS DEVELOPMENT VIA POMC

THE THERMODYNAMIC PROBLEM OF CONSTRUCTION OF THE HUMAN BRAIN FROM VERSION 1.0 FOUND IN CEPHALOPODS:

One of the most amazing things about the human brain is that it is capable of performing trillions of computations during consciousness while using a very low power voltage—on the order of 20 watts. No one knows how this process happens.

If you have any light bulbs in your house, you will see that even your refrigerator light bulb uses more power than your brain, and it can only turn light on and off when the door opens.  When you have a basic understanding of how one can engineer a low-power computer with a lot of computer memory, you will then need to know a little bit about Noether’s theorem, mass equivalence equations, and the controlling magnetic domains.

KEY BLOG POINT:  At 16:32 in the video above, you discover why melanin and water are the ultimate heat engine.  The Carnot theorem is deeply buried in the tissues of all mammals.  Mammals absorb light and turn it into heat, rapidly transferred into the water to be buried at the electronic and vibrational level of mammalian cells.  Water touches every level of where wide-band gapped semiconductors are.  No part of biology is untouched by water.  This is why time is a unidirectional arrow in life.  Energy flows from hot to cold.  This includes light energy from the sun.  This defines entropy.  So when melanin degenerates, the energy buried in water cannot get more energy buried into it.  This means the semiconductors become starved of energy = fibromyalgia, cognitive fog, TBI, PCOS, NAFLD, and obesity.  Get it.  Melanin renovation solves the entropy story in all mammals.

Most people know that computers use magnetic drives to store memory in digital form.  The problem is that magnetic drives are the energy hog in computers, and it has been a real problem in extending the battery life of computers or, for that matter, any technology that uses batteries.  So far, in the technology industry, they have tried to better the situation by improving battery technology and using lithium-based batteries, but this is problematic because these batteries cannot be safely shipped via planes all over the world because of their vulnerability to explosions and fire. (Carnot)

I have told you that as part of the three-legged stool, light, water, and magnetism in Energy and Epigenetics 4,  all life organizes around these three concepts.  In fact, the atomic and molecular organization of the cell is critical in understanding these foundational principles.  So, how does the cell maintain “battery power” across all the collagen and water semiconductors in the human body? ATP is the first layer of energy generation but it is not the most important.

There are 2 main processes that determine health, illness, and body composition for humans.   You must increase your ability to collect photons or you can increase your magnetic moment by capturing as many photons and electrons as you can in your life.  To begin with, the tissues in your body must be put in a position to collect photons and electrons.

This aspect of health is 100% controlled by proper circadian signaling of the environment sensed by the brain. Then, you must be able to assimilate or catch the electrons and photons to stream and move them in semiconductive circuits where they are needed within your internal power grid.  The wide band gapped semiconductors I have described to you in this series create stronger light inside of you than the sun provides to your body.  This light has to be captured to be made useful.  The topologic insulators within you, like melanin, help you accomplish that task. Your brain captures DHA from the marine photosynthetic chain and puts it in the cell membranes of the retinohypothalamic tract before the melanin targets.  Cortisol via ACTH from POMC slows the immune response, and the breakdown products of DHA, resolvins, protectins, and maresins stop the inflammatory cascade and begin the recovery and wound healing part of the cascade in the immune system.  POMC controls both arms of immunity.

Interestingly, when mitochondrial redox is low, and heteroplasmy rates are high, DHA is not efficiently transformed into resolvins, protectins, and maresins.  DHA also lowers SCD1 to push biochemistry from the highly inflammatory omega-6 pathway into the omega-3 pathways, stopping inflammation and beginning wound healing via resolvins, protectins, and maresins created from the omega-3 fats. This is also true in older people who take exogenous DHA. Taking DHA, in that case, has no benefit and may hurt people who have built-in poor redox chemistry at the tissue level because of mtDNA dysfunction that limits the VUV-IR-A at our wide band-gapped semiconductors.  DHA also provides a break in inflammation to allow for wound healing.

At life’s genesis chaos has to gain order. Dissipative structure theory really aims to solve this problem for cellular biology. It uses AMO physics to get the job done.  Remember that stored energy in cells is coherent energy in water. The organism is, therefore, a highly coherent domain possessing a full range of coherence times and coherence volumes of energy storage. This keeps it far from equilibrium and makes it a highly dissipative system of organization.

This arrangement allows us to capture photons efficiently.  In this atomic arrangement, your cell membrane becomes an antenna for the electromagnetic force found locally in your environment.

Like most things in the technology industry, the new technological advances are based upon an expanding knowledge of solid-state quantum physics.  The ironic finding is that Lady Evolution has been using this epigenetic tool chest to build us for 4.6 billion years with her quantum blueprint as well.  The problem is today, in centralized science, few people know it.  The human brain uses many photoelectric switches in proteins to control light & water’s magnetic domains in our tissues.  In the human brain, this innovation in neurons and cerebral spinal fluid has had spectacular returns on equity for Nature. Humans also benefit from this arrangement in the extracellular and intracellular spaces because the water flows between neurons and glial cells become controllable by light frequency changes to lower power consumption.

POMC allows the transmission of electromagnetic waves into tissues to create a time-varying media for biology.

POMC translation into tissues changes the crystalline nature of tissues because the chemicals cleaved by POMC create massive amounts of electrons.  This allows different frequencies of light to be captured and be made useful physiologically.  What are the implications of this ability?

Time reflections in tissues occur when the entire medium in which an electromagnetic wave travels suddenly changes course. This causes a portion of that wave to reverse, and its frequency transforms into another one.  This means that we will see different flickering colors within a material.  It also implies that tissue has to be littered with many different proteins that are able to respond to the creation of different colors.

• For more than 50 years, scientists theorized that an electromagnetic wave could be reflected temporally—not just spatially.
• Scientists have been unable to confirm the existence of time reflection due to the amount of energy required to create a temporal interface.
• Understanding Noether’s theorem helps make sense of this phenomenon in biology.

The explanation of spatial reflections—whether by light or by sound—is pretty intuitive. Electromagnetic radiation in the form of light or sound waves hits a mirror or wall respectively and changes course. This allows our eyes to see a reflection or echo of the original input. However, for more than 50 years (since 1971), ​scientists have theorized that there’s another kind of reflection in quantum mechanics known as “time reflection.”

Energy is understood well in physics because of Einstein’s mass equivalence equation and Noether’s theorem.  Energy is a physical concept but is not really explained well in biology. We know what E=mc^2 means, but what does her theorem tell us?

Emily Noether taught us that with respect to energy and momentum in the universe, light energy “informs” space and time how to curve.  Space and time inside of a cell link to Fermat’s equations of how light travels in a medium.  Fermat’s principle states that “light travels between two points along the path that requires the least time, as compared to other nearby paths.”

From Fermat’s principle, one can derive

(a) the law of reflection [the angle of incidence is equal to the angle of reflection]

(b) the law of refraction [Snell’s law].

I discussed this recently in a podcast with Sarah Pugh, Ph.D. of the UK.

Noether’s equation says that any symmetry, either local or global, implies there must be a conservation of some physical quality in reference to energy transformation to keep the system functioning.  Mammals break TIME symmetry by conserving and amplifying POMC biology in their tissues.  The POMC is translated the more light and charge can be stored at the vibrational and electronic level.  POMC is only translated by “specific frequencies of light in the UV range but cleavage decisions are made by other frequencies of light. Most people have no idea that just about everything I post about POMC/melanin falls directly in line with Noether’s idea in biology.  They will soon.

The big question right now should be in your head why have scientists worked toward recreating this theoretical time reflection in a laboratory experiment? This process allows more minute control of electromagnetic waves and it can vastly improve wireless communications which would lead to advancements in low-energy, wave-based computers.

Nature did this long ago with cephalopods 10 million years after the Cambrian explosion and this process was refined by the evolution of the nervous system all the way into the mammalian clade.  Humans today have the latest refinement of this process in the skulls and it was driven by POMC biology and wide-band gapped semiconductors that could take visible light and use it to change it to light frequencies more powerful in our interiors via the innovation of light chromophore proteins (melanopsin, flavins, B12, B3, NAD+, Vitamin A, Vitamin D, etc..)  so that this light could be captured by our melanin sheets deep inside our tissues for physiologic use.  This process explains how the human brain only needs 20 watts to operate.

In other words, Noether’s theorem allows us to know everything there is about electromagnetic waves—both forward and backward.  When melanin is renovated, the right side of the top level of the slide below allows cells to go right to left and REGENERATE thermodynamically.

We can regenerate melanoma, PD, or anything else tied to it because of the ideas in this blog and the video above.  When you hear the podcast I did with Sara Pugh, Ph.D., be ready for shock waves.

At 54:30 from the video above.  Melanin is “the tokamak” of the quantum cell.  Quantum engineering of Nature was perfected in mammals.

 

ENERGY IS BURIED AT THE ELECTRONIC LEVEL IN CELLS

The energy derived from the sun is stored coherently in cells and ready for use over all space-time domains. Sunlight is transformed by semiconductive proteins into electrical signals. Mitochondrial water production is critical in the blueprint.  How cells transform solar energy is 100% based upon QFT/QED and not the classic biological dogma all physicians and scientists learned in their training. These semiconductive proteins in our cells have side groups that have special molecular abilities.  The primary and secondary protein structures are determined by the DNA code. This relationship maintains the selection of proteins that are capable of a specific type of semiconduction (hydrated wide band gapped) essentially dictates how cell water can or can not bind to the backbone of the protein to work. The instructions for this blueprint are built directly into the DNA and RNA code. No other energy is needed to maintain this organization. This binding has huge implications on how biochemistry can or can not act within a cell. Tertiary and quaternary protein bending is required for final tissue-level physiology.  This protein bending requires accurate timing by using incoming solar energy to the organism via the eye and skin.  This is where POMC becomes very important in mammals. Deciphering signals in light can happen at night time because light energy is stored in the cell’s protoplasm when the sun is not present.  Melatonin is a great example of this.  An inability to transform energy is why bent proteins seem to be found in cells that have poor optical control and show up in many neolithic diseases today.

Consider ATP as an example.

ATP is a natural electron-withdrawing protein, so its “real purpose” in a cell, organized in a quantized fashion, is to strip electrons to make proteins more positively charged.  The waste product of ATP is adenosine and this is a signal that tells the brainstem it is time to sleep. When a protein gains electrons, it becomes reduced, and its charge changes, and when it loses them, it becomes more oxidized, and its charge density changes as well.  Since proteins can both gain and lose electrons in this way, they can vary their charges between these electronic states, making them very reactive to low electromagnetic forces.  This confirms the ideas of Albert Szent Gyorgi in 1941.

He predicted in 1941 that proteins are capable of semiconducting electrons when you look at their atomic molecular arrangements. He had no idea how protein bends, water, and atomic arrangement around the protein bends could be changed to control the actions of chemicals in biochemical pathways. He won a Nobel Prize.  This molecular arrangement in cells allows for the creation of low-powered currents to gain directionality in tissues.  This directionality links to the flow of entropy laid out by Carnot’s theorem above. Becker found when you renovated melanin with the DC electric current in animals, regeneration was possible.  Becker found this in his regeneration experiments in the CNS and PNS on salamanders, frogs, and humans.   This alteration of charge density is a critical point to understand because the charge is a conserved quantum mechanically.

What about some other biomolecules?

MELANIN + DHA + NAD+ + sunlight + heteroplasmy rate = optimize Kleiber’s slope line for humans.  Anyone who tells you that Artificial Intelligence or any supplement/drug will substantially increase longevity does not understand the thermodynamics of life. Water is the key to Kleiber’s law because melanin dumps its entropy into water for further physiological use.  The intrinsic value of vitamin B3- which is derived from  NAD+ of cytochrome one leads to atrophic skin.  When you use exogenous NAD+, it leads humans to a hyper-photosensitivity to sunlight.  This is why so many are solar-sensitive or are told they are “allergic” to the sun.  The reality is that they are deficient in NAD+ & have horrendous redox. NAD+ captures electrons and protons for mitochondria.  This lady below was using NAD+ analogs to cause her skin changes.

SUMMARY

It turns out that photons and magnetic fields have innate solid-state effects which depend less on the energy of the field within the environment than on the ability of the field to orient molecules and atoms with light and magnetic moments.  This sets the stage to develop quantum coherence in tissues and the development of the conscious state in life.  As such, this gives them the possibility, based upon their ability to deflect moving charges.  This ability is directly proportional to how well the 3-dimensional arrangement of the molecule, with the magnetic domain, can break symmetry in the system.   Water is the ideal symmetry breaker in biology.  The asymmetry of the water molecule is due to the 105-degree bond angle between the two hydrogens in relation to oxygen.  This arrangement leads to a dipole moment in the symmetry plane pointed toward the more positive hydrogen atoms.   In physics, however, symmetry means uniformity or invariance, or “the existence of different viewpoints from which the system appears the same” (Anderson 1972). Symmetry breaking is the process by which such uniformity is broken, or the number of points to view invariance is reduced to generate a more structured and improbable state.  This new state requires that energy be transferred.  What emerges from a break in symmetry is a new emergent property of matter. Water changes things.  It is a molecular adapter that transfers energy to different forums for use.

It turns out water has this built-in ability because it is a perfect molecular magnetic dipole.  It is asymmetric because of its binding angles.   This is why just about everything can be dissolved in water.  Water has the ability to transform into many forms itself, and it can transform many other sources of matter into something else quite easily.  We use water’s asymmetry to break electrons from oxygen everywhere in our body.  This means water is the perfect molecule to break symmetry in any thermodynamic problem.  This should be no surprise to anyone with a basic chemistry background.  Life & longevity are fundamentally thermodynamic problems.

Most people are not interested in learning what truth is. They would sooner sit in front of a box that continuously spits out lies and misinformation and entertains them. Why are we addicted to distraction in this modern world?   Is it our weakness, or is it done to us by design? Is it possible that all profound distractions open certain doors in our imagination? Do we have to allow ourselves to be distracted when we cannot concentrate or focus on the reality of what is happening around us? Might it be that our dreaming imagination self seeks to tell us something your waking ears refuse to hear or accept?

Right now, longevity perspectives are dominated by mTOR biology.

Why is mTOR biology operational from yeast to mammals but not human mammals? The answer is in the way humans use POMC biophysically. Sabatini has no idea how glucose, oxygen, and phosphorous operate upstream of human mTOR, but he admits it publically when he speaks and I respect that. My podcast with Rubin and Huberman answers it. Wide-band gapped semiconductors make the light that controls the entire pathway rostral to Sabatini’s discoveries 28 years ago from Easter Island.

HOW DO YOU TAKE YOUR ONE SHOT?

The past three years have enraged me.  It was bad enough that I had to endure 30 years of centralized medicine bullshit, but the debacle of COVID and the follow-up mRNA fiasco was the whipped cream and cherry on a shit Sunday.

Sometimes, life allows you to take your shot or leave the opportunity in your bag.

Golf and Nature have a lot in common.  I never realized it until this summer.  I went to a health event and was allowed to change the world.  Every struggle and success in my life brought me to this moment.  The meeting had Chatham rules in place, but one of the organizers, Clusk, broke his rules and filmed and taped the talk.  He told me later that he thought the moment might be essential to get into the can. Life is a game that cannot be won. It can only be played.  No one is getting off this pale blue dot alive.  But we do have time to make a difference.

Sometimes, you have to play your game and no one else’s.

I remember standing there with my nurse right before my talk, and she nervously turned to me and  asked, “Are you ready for this?”

I looked at her and said, “They better be.  Because this is going to be epic.  Just watch what you can do with my one shot.”

I was due to speak three days earlier, but they kept pushing me off because the universe was summoning me to do something interesting with this opportunity.

Might the El Salvador administration decide to prove the world wrong again in healthcare?

In the audience sat a man with a leather notebook who took his place to my left as I began to chop wood.  As soon as I spoke, he began to write.  The more I said, the more furious he wrote.  Soon, the audience was leaning toward me, and with each passing slide and topic, they got closer to the edge of the seat.

By the time I was done, they were standing and roaring at the Palestra Society.

The man with the leather book rushed to me and wanted to speak.  He said a lot, and I told him that if he wanted to change his country, he should get up at 5:30 AM and meet me on the black sand beach of Mizata.  He did as the picture below shows.

As we watched the sunrise, he told me he wanted me to help his country with a problem.  He thought I might be able to solve it.  The administration wanted me to write a Constitutional Amendment to separate the state from medicine to bring real medical freedoms to the people of El Salvador.  He told me that the government anticipated a big win for their policies in February of 2024 and that they may be given a mandate to do this.  He told me it was time to leave the shadows of my locked cage in centralized medicine.  It was time for me to choose………how to play a new game.

They wanted my best ideas to decentralize medicine in document form.

In a centralized world of volatile situations, I had to stay calm and focus on the task. That was the key to getting this done on time.  I had to maintain composure and concentration, even in adversity.  What was my mindset?  I am an American doctor whose entire professional life was built around the injustice of not having fundamental medical freedoms and informed consent.  So, with this mindset, I set out to create a law to break the rules that are allowed to exist in America to harm doctors and the public.

America has no medical freedom laws in its founding documents, and it has created an attack angle on the Republic that COVID has exposed.  American freedoms solely rely on the 1st, 2nd, and 4th Amendments to protect the public, and the current political parties and industrial-military complex are hammering heavy machinery at all those pillars of protection.  They do it to gain more power and control than our Founding Fathers granted them in the Constitution.   Thomas Jefferson realized how important violence was when he made the Second Amendment.  US history with the King called for it.  El Salvador’s history does not.  Their 1st civil war scared the public of guns, and their second civil war with the gangs made them suspicious of guns,  but both created a more significant need for medical freedom laws without a Second Amendment.

Violence is not a solution; sometimes, it is a necessary evil when changing a culture.  Jefferson learned that from his time spent in France.  This idea encapsulates a complex and controversial aspect of human nature. While acknowledging the inherent destructiveness of violence, the idea buried in freedom recognizes that there may be instances where its use becomes inevitable. In extreme cases, such as self-defense or preservation of life, there may be no alternative to resorting to violent means.  El Salvador has chosen a path different from our Founding Fathers’, as President Bukele clarified in his CPAC speech.

Sometimes, breaking the rules is the best option when your goal is to achieve justice in another location.  It highlights the hypocrisy of your discomfort for the world to see.  This is how entropy in a refrigerator works.  The appliance is engineered to cool temperatures inside to protect the food and make it last longer, but it dumps the heat back into the room behind it.  Net entropy in the world remains the same, but something good is happening inside the appliance.  This is how I look at El Salvador.  The USA is the kitchen.  It is filled with heat, and food rots there more quickly now.

My Constitutional Amendment highlights the complexity of ethics in how the state deals with healthcare and the importance of prioritizing the greater good in every section of medicine. While society often emphasizes the need to abide by rules and regulations, there are situations where strict adherence can impede justice. COVID-19 highlighted this globally, and Bukele reacted quickly to right a wrong.  When the existing rules fail to deliver fairness or deny fundamental human rights, it becomes crucial to question their validity and, if needed, challenge them, then change them.  This is the task Nayib gave me.

Breaking specific rules of governance in the USA creates freedoms that can be experienced in the Ark of El Salvador.  Suppose it aims to achieve justice in a tiny corner of the world.  This is what the Age of Light is all about.  President Bukele hopes the light El Salvador emits on medical freedoms will have an abscopal effect on the other 195 countries worldwide so they begin to follow his lead.

Medical freedoms must be separated from the State at all levels to protect public health.

In that case, it can foster progress and positive change globally over time when people see how it changes society in El Salvador. However, the ideas in this amendment also underscore the delicate balance between upholding the law and pursuing justice, urging individuals to act responsibly and consider the consequences before taking such measures.

During sunrise that August day, he told me the story of Jack Mallers and how the same group of people tasked him to write a law for legal tender status for a Constitutional change to the Republic of El Salvador.  He told me to be ready in 24-48 hours to sit down with President Bukele and give this talk to him face to face.  If the talk hit the mark, he felt the President would ask me to amend the Constitution on medical freedoms.  He told me Jack took two days to write his legal tender law before he met with the President, and they understood my law would be much more challenging to write because it was a more complex task.

I looked up at him and told him I would have the law written for him by sunset that night.  I have lived 30 years under the tyranny of centralized medicine, and writing this law would flow out of me naturally.  I left Mizata with my orders and sat in Playa Shalpa in the sun for 5.5 hours.  I wrote the law with the help of my nurse, Chantal.  She had crafted a skeleton of our ideas for over 30 years in medicine.   She was the perfect person to do this because she has been an OR nurse and legal nurse consultant for thirty years.  She has lived through the same environment as I have that the industrial healthcare paradigm created.

I banged out the law on the same computer I am typing now and called several of my physician friends I value for input on certain parts.  I was done about 30 minutes before the sunset, and Chantal wanted to proofread it.  She did, and I sent it to two attorneys to see if they thought it was good enough to send to the Bukele administration.  One was an El Salvadorean attorney who did not initially support Bukele’s administration.  The other was a US attorney working on getting some Bitcoin laws done for exchanges in El Salvador.  None of them could review the law before sunset to my satisfaction.

You might recall that some of us had the temerity to ask questions on social media about the efficacy of using PCR as a diagnostic tool for COVID-19 infection. Click the link you just passed.  For some of us, that’s because we used the PCR technology in our clinical work; for others, they were aware Kerry Mullis, a Nobel prize recipient due to inventing PCR, said you can’t use it that way, particularly if no attention is paid to cycle number.   You DO remember that. When we asked if the cycle numbers were consistent and transparent? Remember when they dialed the cycle numbers down once the vaccine was rolled out as they no longer wanted everyone to be infected bc with a sufficiently high cycle number, you can “find” anything?  Yeah, I sure remember all of that when I wrote this law.

I had a small group of my tribe there witnessing history.  When I was done, I felt a bit sick to my stomach.  The largess of this task in an afternoon hit me all at once.  I told the people around me I thought I was missing something big.  As I sat back and looked at the sun dropping into the Pacific Ocean, it downed on me the profound impact a single act can have on our lives and the lives of others. Often, we underestimate the repercussions of our actions and fail to consider the potential consequences they may bring. In a world where actions are increasingly swift and impulsive, it becomes essential to pause and reflect before we act. Thinking and reflecting before we act allows us to weigh the potential outcomes, evaluate our motivations, and make informed decisions. By doing so, we can prevent unnecessary harm, foster positive change, and ensure that our actions align with our values. I realized I was worried about making a mistake that could harm and not help the public.  From reading C.S. Lewis, I knew that more evil had been done to humans with good intent.  Embracing this philosophy encourages personal growth, mindful interactions, and a more harmonious world.

I re-read it and said, this is my best shot to change medicine.  I felt it had all the feel of a law Benjamin Rush would smile at.  Then I hit send.

The law got to the Bukele administration, and they met and talked about it.  Twenty-four hours later, I was summoned to the Capital to meet with Nayib Bukele and his brother.  He told me I had made an impact and wanted to hear more, so I gave him his version of why decentralized medicine requires medical freedom laws in a Constitution.  I warned him about the news coming in the USA that viral contamination would be breaking soon, and I was going to meet with RFK Jr in Malibu to discuss it in October of 2023.  This was in August of 2023.  None of this data was known at the time.  I was made aware of data that was related to the documentary I did on Covid two years earlier, where I warned the public that having two legal definitions for the Pfizer vaccine was a warning that the vaccine company was planning two separate versions of their gene therapy product for some reason and that we should be vigilant at looking at their patents and science.

I tested all his lights and nnEMF in the house and told him we had some work cleaning up his place because the world needs his brain optimized.  He is building an Ark of Freedom for his people.  He did it first with money, now with medicine, and soon you’ll see his following freedom policy in 2024.  I feel hope again for medicine and the public good.

We were only supposed to meet for 30-45 minutes because he had dinner set up with his mother and his family, but twice, he called his mom and delayed it because he felt we were not done.  Three hours in, we were done.  He told me he was going to move forward with his cabinet and give the law to the legislative body to get it formatted to be presented for passage into the Constitution.

I got back into the Presidential limo, and as the soldiers drove me back to the Hyatt Centric in San Salvador, I sunk into the seat, thinking about what I had just experienced.  I thought about the Federalist Papers and the three-way conversations between Benjamin Rush, Thomas Jefferson, and James Madison.  Then, I thought about our three-way conversation earlier that night.

I have been an angry surgeon for 30 years because I had no hope for change in my profession.  In El Salvador, I found my medical savior.  No matter how dark the nights of trauma call have seemed in my career, the dawn always comes. Hope is a powerful weapon for change.

For the first time in my professional life, I realized I was not alone. The Bukele brothers understood my struggle, and that night made it all worth it. They understood what being caged was like.

I remember thinking what Bagger Vance said to his golfer about taking his shot.  He said, ”  You can do this, yes you can… but you ain’t alone… I’m right here with ya’… I’ve been here all along… Now play the game… Your game… The one that only you were meant to play… Then one that was given to you when you come into this world… You ready?… Stike that ball Junuh don’t hold nothin’ back give it everything… Now’s the time… Let yourself remember… Remember YOUR swing… That’s right Junuh, settle yourself… Let’s go… Now is the time, Junuh…”

I felt at ease for the first time since I graduated medical school that night.  It was a surreal feeling.  I slept like a baby that night.

For the last eight months I have had to harness this energy and focus it on getting ready to break this news to the rest of the world.  This law exposes many problems in the centralized world.

SUMMARY

There’s no science without scientific debate. It’s too bad that open discussion was replaced by censorship in the world.  Today, El Salvador is pushing back on that trend.

I wrote this Amendment with something important in mind.  Contrary to popular belief, justice is not solely about punishing the guilty but rather about safeguarding the innocent.  As much as I want to bury the treasonous in the USA, my job in El Salvador is medical protection.

The great viruses of our time spread through minds, not through bodies. They spread via narratives over social media sites.  We must change the way science is done.  I’ll have something to say about that in the law and on Saturday when I speak to the world on this topic.

The decentralized method to the scientific method will eliminate the need to Universities or the parrots of that paradigm who run podcasts.  You have my word on that.

Science isn’t ‘what experts think.’ It’s a method that corrects what experts think. If your doctor continues with the groupthink present in centralized medicine, you have a duty to help free yourself from the chains of tyranny.  Come to the Ark for a visit.  See what we are doing.

Golf and Nature have a lot in common.

Every sunrise is putting your eyes on your prize in life.  It gives you the chance to play your own game in life.  It is all well and good to watch others play their game. You can live your life by putting your eyes on Bobby Jones.  You can observe his practice swings.  If you’re paying attention, you can almost hear his thoughts and know he is searching for something.  Then, in a moment of Eureka, he finds it…

He is now in perfect resonance or harmony with his environment.  One authentic shot and that opportunity might choose us for this moment.  It is as if there is an ideal opportunity in the world, and it is trying to find each of us.  All we need to do is get out of our own way and let it happen.

To manifest this destiny, all it took was going to a place where the seasons and tides of the ocean met perfectly with the revolutions of the Earth and the politics.  With this shot, you might not initially see the flag on the tee box, but you know that flag placement is a dragon you must slay.  You have to use your best sense, and seeing is not always the best one to choose to use.  Sometimes, you must feel what is right before you take your best shot.  Sometimes, opportunity knocks once because the universe comes together in your presence, and things become whole in your soul.  You feel the cosmos resonating inside of you.  It guides the ball to the flag.  Your eyes are almost redundant at this moment.  The flight of the ball moves with your soul.  You seek it with your hands as a surgeon because that is how surgeons do it.  They feel it before the act.  Our hands were trained to be wiser than our minds.  No person could take us to this moment, but many people in your life hoped you would find your way home to that flag.  Your success becomes their success.

WHY EL SALVADOR?

Why not when the US Congress has become a circus?

Look, if you had one shot or one opportunity. To seize everything you ever wanted in one moment. Would you capture it or just let it slip?

I HAVE BEEN CHASING THIS CHANGE FOR 20 YEARS

Humans evolved the attributes of a large brain and the ability to speak, forming an intricate social network that can use many aspects of technology. Our most significant attribute is the ability to think. This allows us to change the environment we are adapted to radically. It has allowed us to dominate all habitats and create havoc in most of them. The real human miracle of our mind is not that we can see the world as it is…but that we can see it as it is not and then change it. If we think and act incorrectly, we can quickly recalibrate and overcome it. Conversely, we seem to be a prisoner to our paleo-cortex (older, less evolved brain) and resist change even when we know it must occur. We often subjugate the best interests of our survival to suit our emotional needs or desires. The fundamental paradox of humanity is that our reasons for what we do are often weak but our sentiments to do them remain quite strong. Interestingly, we have overcome that liability as a species so far many times. Some of us even find comfort in that ability at times.

I believe today, we are mismatched in our environment because of our own doing. We all know that when we eat poorly, we make a decision that could ultimately kill us, albeit slowly.  Few of you realize that when your environment is mal-illuminated, it can make you sick and kill you rapidly.  Mal-illumination > malnutrition in terms of medical risks.  The AGE OF LIGHT event in El Salvador aims to change your perceptions tomorrow.

I watch “serial suicide” daily just by walking through hospitals and when I drive by the fast-food drive-throughs and visit the hospital cafeteria. That irony is not lost on me, either! I think LIGHT is far more insidious and sinister because it allows our mind to be unaware of the implications of that choice.

How else can you justify a lifetime of the Standard Western Diet under LED bulbs when your countrymen are dying of chronic diseases that now occur in teenagers? I recently read a comment on Twitter that motivated me to write about this human ambiguity. She commented, “My parents ditched all their incandescents to put LEDs in to save money.  Why?  They eat more prescriptions than they do food, and they have to budget with rising costs. They do not think their food choices ultimately affect their health. They bought a Wii for exercise in the house and only play video games on it. They never go out in the sun anymore.  They are pale, frail, and decaying in front of my eyes.  They BOTH work in the medical field too.”

Today, the game has changed.  GAME SET MATCH.  It is time to change the world of medicine.  Above you see the founding partners of this movement.

I want to embrace where the human species is today.

1 in 6 people globally affected by infertility.  The number is close to 2.5 out of six in Americans.  I consider infertility in humans as I would consider a mutation in DNA or mutant disease.  Today we know we can rescue fruit flies from their genetic fate using light.  The science of optogenetics is telegraphing us that our use of light today in technology is a huge problem.  This implies that light maybe behind why humans are becoming infertile at record rates in a modern world that is blue lit, filled with RF and microwaves pulse radiation while blocking the healing rays of the sun in the visible spectrum.

Did you know oocytes have some unique characterisitics when it comes to light?  Melanin levels in cells seem to control their backround fluorescence.  When melanin is absent in a low concentration this decreases the intrinsic fluorescence of the oocyte.  Conversely when melanin levles are raised in an oocyte,  this increases the fluorescence of the oocyte.  I’d like you to recall that in disease states associated with higher heteroplasmy, eukaryotes release more light.  In health they tend to conserve their light release.  Given these facts, do you see something unusually about the mammalian oocyte?  Females are bron with all their eggs and this cell is the largest cell in their body and this cell is actively emitting UV light.  This seems counterintuive to the centralized mindset.  But it makes perfect sense to a decentralized thinker.

Melanin is a useful molecule in the lab for suppressing background fluorescence due to its wide range of absorbance of electromagnetic signals.  In fact, it is well known in the literature that the expression of melanin in oocytes causes the animal pole to be darker visually and more light absorbent and thus have less fluorescent background compared with the lighter-colored vegetal pole.

Did you know human females at birth limit melanin in their oocytes?  Did you know at puberty they change their melanin expression by using salt induced kinase inhibitors to increase melanin production in the oocyte which acts to conserve ultraweak UV light release during ovulation.

Salt-inducible kinase (SIK) inhibitors has been demonstrated to regulate the activity of the transcription factor CREB which is linked directly to the clock genes, and it plays a key role in controlling melanin pigment synthesis in the skin.

Do you know what kind of melanin the human oocyte makes to run this script?  Did you know that neuromelanin is created from from regualr melanin stores in the neural crest derivatives from the oxidation of dopamine?   (Zeise et al., 1992)  Did you know that oocytes are loaded with dopamine?

Did you know that centralized science has no idea what oocytes are loaded with dopamine?

High levels of dopamine (DA) have been described in human ovary in 2005 and we now have  evidence for DA receptors in granulosa and luteal cells, as well. However, neither the full repertoire of ovarian receptors for DA, nor their specific role, is established.  What if I told you, the purpose of the dopamine was to age the germ line faster than the colony of the mitochondria in all other cell lines in a woman.  Would you buy this?

It turns out mitochondria have small-molecule salt induced kinase inhibitors (SIK inhibitors) that when generated by endogenous light signals of the oocyte induce a topical change in melanin in an oocyte.  Few people know that humans can inducing cutaneous pigmentation independently of UV irradiation in human skin using alterations in your salt concentration.  I warned my audience about salt changes and UV fluorescence in my Vermont 2018 talk but y’all wanted it all dumbed down.

Well, soon you’ll get the implication of the decentralized  wisdom I gave in you 2018 Vermont with a new biophysics education on Patreon.  Mujahid et al. 2017 was a key paper in me figuring out why infertility now affect 2.5 out of six Americans.

Is fecundity, fertility, and successful pregnancy all linked to circadian biology via melanin and melatonin biological control over apoptosis and autophagy in mitochondria?  The answer appears to be a big YES, if you read the literature.  This has huge implications for extinction level events in anything that alters melanin and melatonin levels in humans.  It is now clear melanopsin function has a similiar effect on the light receptors of man.  Blue light and nnEMF cause photoreceptor extinctions.  I wonder how long it will take the non-Black Swans out there to get this rather simple, yet significant message?

Women give rise to the mitochondrial progenitors in the homo sapiens.  Reproductive ageing in female mammals and women is characterized by a progressive decline of ovarian function, manifested by a decrease in the quantity and quality of oocytes with advancing age. The reproductive tract of women is one of the first organ systems to show hallmarks of ageing, in comparison to other organs.

Exposure to nnEMF/blue light has been shown to lead to early menarche and early reproductive decline.  Human society has radically changed in its use of light to be sure.  But our civilization has also changed globally in other ways in last 120 years.  Women are now part of the work force, and they are delaying a family for their career.  They are using birth control at early parts of their development that impact the circadian clock machinery in the mitochondria of their oocytes.  All of these factors are playing a role in global infertility.  In societies where women are irradiate earlier and often the rates of infertility are higher than we find inmore primative parts of the human clade in other parts of the world.

In women, the reproductive system ages early in life and this represents a key insight to understand how human female age in general.  How you experiene menarche, peri menopause, and menopuase matters to a dectralized MD.

The oocyte is recognized as the largest cell in mammalian species and other multicellular organisms. Mitochondria represent a high proportion of the cytoplasm in oocytes and mitochondrial architecture is different in oocytes than in somatic cells, characterised by a rounder appearance and fragmented network. Although the number of mitochondria per oocyte is higher than in any other mammalian cell, their number and activity decrease with advancing age.

Mitochondria integrate processes essential for oocyte function, such as energy production, biosynthesis, and redox homeostasis.

Mitochondria integrate numerous processes essential for cellular function, such as metabolic processes related to energy production, biosynthesis, and waste removal, as well as Ca2+ signalling and reactive oxygen species (ROS) homeostasis. Further, mitochondria are responsible for the cellular adaptation to different types of stressors such as oxidative stress or DNA damage. When these stressors outstrip the adaptive capacity of mitochondria to restore homeostasis, it leads to mitochondrial dysfunction.  This is how children are born with high disease burdens via transgenerational epigenetics.

Dysregulation of mitochondrial processes have been consistently reported in ageing and age-related diseases.

Reproductive ageing in female mammals and women is characterised by a progressive decline of ovarian function, manifested by a decrease in the quantity and quality of oocytes with advancing age. The reproductive tract of women is one of the first organ systems to show hallmarks of ageing, in comparison to other organs.

Difficulty conceiving and infertility are treated as taboo topics in most nations and lead to significant psychological stress for those experiencing them (Patel et al., 2018). Although assisted reproductive technologies (ART) such as cryopreservation (the freezing of oocytes, sperm, or embryos) and in vitrofertilization exist, they are not ubiquitously available or successful and require substantial financial investment (Katz et al., 2011). Furthermore, a fertilized oocyte derived from a woman of advanced age has a higher chance of resulting in miscarriage, and/or aneuploid offspring like trisomy of chromosome 21, commonly known as Down syndrome (Bittles et al., 2007). With advancing age, a decline in mitochondrial number and function is observed in oocytes. Mitochondria are exclusively maternally inherited and therefore the original population present in the oocyte will give rise to all future mitochondria in the offspring (Jansen and de Boer, 1998). Thus, elucidating the mechanisms underlying the loss of mitochondrial function with ageing and why oocytes age much earlier as compared to other organ systems, may lead to new lifestyle strategies to prolong oocyte fitness and fertility in humans who want to avoid reproductive extinction.

SUMMARY

QUESTION:  When you read this blog what is your gut reaction?  Just think about that answer now.  I’ll share my thought as I wrote it below.

Disturbing the molecular clock in animal models leads to abrogated mitochondrial rhythmicity and altered oxidative respiration. Moreover, mitochondrial-dependent production of reactive oxygen species (ROS/RNS), which plays a role in cellular signaling leading to early aging in different tissues.  It has also been linked to the circadian clock mechanism dysfunction.

Note in the above picture and its description how the ROR receptor for Vitamin A begins the ticking of your circadian clock mechanism.  What does blue light and nnEMF all liberate from opsins?  Vitamin A.  You starting to see my perspective yet?

My gut instinct tells me the light used in technology has been cultivated as a means of human behavioral & population control. Future militaries will consist of AI, drones, robotics, and lasers and it will be turned on We The People, and not the enemies of the state.  Today’s humans are the enemy of the political class. Humans, if they continue on their current trajectory, will be reduced to the status of cattle.  Your government is cultivating you for a future they are building for you at your expense as you reach out your hands to allow the handcuffs of technology to be placed on your wrist no fight or revolution.  It is Plato’s Allegory of the Cave circa 2024.

Is there a way to tan your body without the sun if your child has precocious puberty?  Yes.  I have taken on new Farm clients for this treatment in 2024 on a case by case basis.  Work by Mujahid et al. recently published in Cell Reports has described how topical administration of first and second generation SIK inhibitors, called HG 9-91-01 (HG), YKL 06-061 (YKL1) and YKL 06-062 (YKL2), can increase melanin production in vitro and in vivo to reverse the effect of blue light toxicity in high risk young adults and children with these risk factors.  

UV from the sun induces tanning in keratinocytes and it engenders the production and secretion of alpha-melanocyte stimulating hormone (α-MSH) from POMC, which binds to the melanocortin 1 receptor (MC1R) in melanocytes. The subsequent increase in cAMP and activation of protein kinase A phosphorylates the cAMP-responsive-element-binding protein (CREB), resulting in increased microphthalmia-associated transcription factor (MITF) transcription and increased melanin production.

This is a new way to help people solve massive problems from tech abuse in infertility and precocious puberty.  I did not include it in the Melanin Renovation Rx because it requires a knowledgeable MD to optimize the process.

CITES

1. https://www.cell.com/current-biology/fulltext/S0960-9822(20)31073-3

2. Mujahid N, et al. A UV-Independent Topical Small-Molecule Approach for Melanin Production in Human Skin. Cell Rep. 2017;19(11):2177–2184.

 

The video above gives you large brushstroke ideas of what quantum biology is to one of the pioneers in the field.  In this blog, I want to provide some other ideas that go further than his.

Restriction of food intake to defined time periods is known to change the phase of the circadian clock and gene expression programs in humans, especially in primary metabolic organs such as the liver.  This is why fatty liver is a disease of light and not food.  When I read these papers in 2005 I wondered if this relationship exists within the liver what about the skin?

The skin envelops our body.  It is where the environment acts to meet with our tissues.  For this reason, it should be a place where quantum biological processes can be found to help create the correct state for the “trickery” of nature to work with our cells.

One of the most counterintuitive facts in skin biology is that AM light, dominated by red light with a paucity of UV, somehow protects the skin from future UV skin damage.  This fact tells us that some trickery is happening inside the skin’s tissues, and red light photons induce this trickery.  Might there be some other trickery with the skin about another solar signal to protect it from UV light?

WHY DOES THE LEPTIN RX have this peculiar relationship to breakfast timing?

Food, at its core, is matter that encodes information about light via photosynthesis.  Because of this insight, I began to examine how the informational bar code in food might alter the transcriptome of the skin.  What I found was stunning.  Light and injury affects all the clock genes in our skin.  With that the Age of Light began in my head.

When I went deeper into this rabbit hole I also found out I could use hair as a measure of disease reversal.  If you go back and re-read the Leptin Rx go look at what it says about sweating and hair return.  Now you are beginning to see the wisdom of that simple blog.

I found that time-restricted feeding shifts the phase and alters the amplitude of the skin’s circadian clock mechanism in humans.  This is why the 30-minute window is part of the Leptin Rx.  Moreover, time-restrictive feeding affects the expression of approximately 10% of the skin transcriptome.  What does it do?  It mimics the effect of red light on the skin concerning UV tolerance.  In other words, if you eat at the right time, UV light loses its toxicity for the skin!

What is the food trickery I built into the Leptin Rx really about?

Eating breakfast within 30 minutes of sunrise creates a time-restrictive feeding window designed to increase the skin’s ability to upregulate the DNA repair apparatus for UV light.  , Many people still have not realized that many skin-expressed genes are acutely regulated by food intake in the morning. AM sunrise is required to improve the fidelity of the circadian mechanism.  The circadian clock is required to reset cells to the default state for daily rhythms in DNA synthesis in epidermal progenitor cells.  I then read this paper in 2015, and it told me my hunches ten years earlier were correct.

This paper implied that our exterior tissues had to have a mechanism built into them to control the circadian clocks of the gut.  It turns out I told the world this in Vermont in 2017.  The following two slides showed these insights to the audience that day.  In 2024, I still do not think most of the world realizes the profound implications of these ideas.  The outside of our bodies uses light to control how we handle food.  This is when I realized food wasn’t as important as I was taught to believe in medical school.  Light controls are far more critical than we all believe.

In the video above, Jim mentioned the 1941 book, “What is Life”. Schrödinger wrote in that book that he believed the heredity material is likely to be a molecule, which unlike a crystal does not repeat itself. He calls this an “aperiodic crystal”.  That was written 13 years before DNA was discovered in 1953.

An aperiodic crystal is a crystal that posses long range order and symmetry. The main property of crystal structure is its periodicity. This periodicity is due to the arrangement of atoms/molecules in the lattice points. The crystal structure as a whole can be considered as the repetition of unit cell.

Why is this a big deal?

Each DNA strand holds dazzling possibilities for biology. When you play with a number of variables the environment can dish out to cells— the molecular make-up of water that surrounds it, the composition of the saline solution that holds it, and even the temperature of the room—can impact what the crystal of DNA looks like.  This ability fortells us it is a quantum computer.  There are many other shapes and forms to be found with DNA and the environment.  It is almost like the Library of Alexandria for life. How will this make a bigger impact on your perspective?  In a lab you can put hydrated DNA in a test tube and just vary the light and see what DNA is capable of in its crystalline form.  When you combine DNA with the variety of optical lighting settings within the microscope, and there are almost endless combinations to be explored in this molecule of life.  Aperiodic crystals exhibit many quantum abilities with respect to light.  Time restrictive feeding is one of those things.

Time-restrictive feeding can induce shifts in the clock phase but does not alter the phase of DNA synthesis.  DNA is an aperiodic time crystal.   DNA crystals form when a double helix is suspended in a liquid that evaporates. They grow in patterns dictated by the information stored within the strands. When seen in cross-polarized light, they display a mind-bending kaleidoscope of color and shape. The vast range of crystal structures in DNA is impressive. (pic below)

WHY DO I ADVOCATE FOR THE BIG ASS BREAKFAST?

That part of the Leptin Rx is also not about food.  It is about light.  I found a way to alter skin biology to allow it to perform some trickery with light.  Time-restrictive feeding alters diurnal sensitivity to UVB-induced DNA damage and expression of the critical DNA repair gene, Xpa.  In 2005, I found that when we eat is more important than what we eat.  Then, in 2017, centralized scientists gave me the data to prove my insights were correct in mice.    I shared them with my audience in my Vermont 2017 talk.   New data indicated that regulating skin function by feeding time in mammals emphasizes a link between circadian rhythm, food intake, and skin health.

They had my TED talk in Nashville banned 15 years ago because Big Pharma knew the GLP-1 peptide drugs were in the pipeline for the obesity crisis.  They did not want the truth out about the leptin melanocortin pathway and how sunlight and cold work on it.

The lies of Big Pharma’s authority are more contagious than any virus, stickier than tar, and will die like a Kraken.  I know my enemies well in this battle.

SUMMARY

Mammal skin provides the first line of defense against many environmental and stress factors for mammals that exhibit dramatic diurnal variations such as solar ultraviolet (UV) radiation and temperature.  Mammalian skin biology provides opportunities for the decentralized clinician to interrogate the clock regulation of tissue metabolism in the context of stem cells and regeneration with these insights.  In fact, mammal skin is most sensitive to UVB-induced damage at night, when expression of Xpa is lowest.  We can alter this with red light therapy and time restrictive feeding built into the Leptin Rx.  Melanin renovation further limits this damage.  The Leptin Rx and the melanin renovation Rx is antihetical to the Big Pharma paradigm in power now.

The centralized medical system insists that they don’t know what causes many medical conditions and therefore they have no known cure. They discourage everyone from seeking a cure until Big Pharma finds the solution that they can take advantage of. They contradict and smear the reputation of anyone who is daring to find any treatment that is not part of their system. The only thing they offer those with mental illnesses is psychiatric medications, which in some cases might make life easier for caregivers, but does not help anyone recover from these illnesses.

Centralized clinicians learn the art of self-delusion in their training.  They convince themselves that we are not letting patients down with the evidence based advice we were spoon fed, because we are doing the “clinically appropriate thing”. Well-meant initiatives in centralized healthcare become misappropriated to justify neglect.  My writing seems to be my personal ipecac, but it makes me feel much better afterward, but sometimes people don’t like the result.

CITES

1. Adamovich Y., Rousso-Noori L., Zwighaft Z.,  Neufeld-Cohen A., Golik M., Kraut-Cohen J., Wang M., Han X., Asher G.  Circadian clocks and feeding time regulate the oscillations and levels of hepatic triglycerides.  Cell Metab. 2014; 19: 319-330

2. Damiola F., Le Minh N., Preitner N., Kornmann B., Fleury-Olela F., Schibler U.  Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus.  Genes Dev. 2000; 14: 2950-2961

3. Kuroda H. et al.  Meal frequency patterns determine the phase of mouse peripheral circadian clocks. Sci. Rep. 2012; 2: 711

4. Stokkan K.A. et al.  Entrainment of the circadian clock in the liver by feeding.  Science. 2001; 291: 490-493