The amount of sleep an organism needs is directly tied to how well the organism deals with “entropy dump” back into its environment. If you do not dump it back into the environment well, you need to sleep more. If you dump entropy back into the environment well, you need to sleep less. No one has that understanding of the purpose of sleep because they do not have my understanding of how a quantum cell works. ----said by Moi, 15 years ago in a blog.
2. Each molecule of ATP in a cell controls 8800 water molecules binding sites and 20 potassium ions, to make metabolic water function as a liquid semiconductor inside every cell. I said this in the podcast 24 hours ago but wrote it in a blog 15 years ago.
A member on my forum recently posed the question, “we hear that ketones are a great brain fuel: they provide more ATP than sugars, burn cleaner, and may possibly be the preferred fuel, etc……….we also hear that ketosis works for refractory seizures and there are case reports and a few small studies showing benefit in autism, Alzheimer’s and possibly other neurodegenerative diseases. It appears most everyone reports sharper cognition and sense of energy/well-being. The confusing part for me is that many people also report poor sleep with ketosis. Why is just changing food, and no other variables, often linked to reports that their sleep worsens? It is a common complaint and I can’t yet make sense of it. Can you explain it to me?
Yes, this explanation came right out of a blog I wrote 15 years ago. Nobody seems to read anymore.
My Answer using Quantum Cell Theory: The answer to this is easy, yet complex, but buried in the science of the Energy and Epigenetics 6 blog post. When you eat a more ketogenic template you make more ATP to maximally unfold proteins. This is based upon the ability of one mole of glucose only making 36 ATP vs 147 ATP from the beta oxidation of fats. ATP’s main function in a zero entropy quantum cell, opens protein conformational structure to expose more water binding sites in proteins.
When this occurs the amount of ATP is stochastically linked to potassium concentration inside the cell. This is why potassium is found inside all cells and sodium is not. Sodium exclusion is not due to a membrane pump as most biochemistry books say. Gilbert Ling proved this mathematically and experimentally close to 50 years ago. The only reason his work was not accepted was because biology does not realize that energy in cells is generated by semiconduction of charged particles that are separated from water. Becker’s proof on Ling’s conceptual framework did not come until 9 years after Ling showed why K (potassium) and Na (sodium) are included and excluded because of the semiconducting currents found inside cells energized by sunlight. This has been further proven in the molecular actions of rhodopsin, melanopsin work in the retina, and actin and myosin in muscle by Gerald Pollack, all using hydrated protein semiconduction.
3. How does physics explain K+ ions and light and water? Brownian motion = statistical motions of atoms Einstein realized this the demon Maxwell was talking about in 1867. it took 38 yrs for someone to make sense of it. Do you know, of Einstein's 4 miracle papers of 1905 that the one on Brownian motion is the one most cited? Yet he won nothing for it.
Maxwell was the first to show that the second law of thermodynamics had to be statistical. Einstein showed Brownian motion was the observation of the statistical event predicted by Maxwell. In the 1950's science really upped this game when transistors and semiconductors were found. Why? any trap door that opens in one direction only and requires a specific amount of energy to open it is essentially a Maxwell Demon.
This gave birth to solid state devices we use today. Rectifiers let current pass in one direction and not in reverse, thereby converting AC currents to DC ones. In the 1960's Becker showed bone had a rectifying current built by light in periosteum. The implication is that these semiconducting gates can randomly convert a fluctuating current of electrons in a membrane into a DC current that can be used to physiologic work. The electrical potential of the cell membranes stores energy of light in the electrons it captures photoelectrically. This is done by Coulomb's law. Membranes are designed to capture electric flux and captures magnetic light flux. This, in turn, excites the electron and it becomes a particle only and loses its wave ability. This is part of the photoectric effect. So an excited electron in a semiconductor can only act as a particle. A delocalized electron has more range to act differently, as a wave and/or a particle.
This idea leads us to one conclusion: the electrical potential difference between two sides of a membrane can be harnessed and used to perform cellular work when ever it is needed. Why can energy be harvested in life anytime it wants it? The photoelectric effect is instantaneous, therefore time is no longer an issue. Photons never experience time, unless they are catured by a semiconductor. Even then, they are moving fast just not at the speed of light. The speed of light in a tissue is the rate limiting factor for a cell.
A calculation shows that the electron is traveling at about 2,200 kilometers per second. That's less than 1% of the speed of light, but it's fast enough to get it around the Earth in just over 18 seconds. In silicon (Si) the electron mobility is of the order of 1,000, in germanium around 4,000, and in gallium arsenide up to 10,000 cm2/(V⋅s). Hole mobilities are generally lower and range from around 100 cm2/(V⋅s) in gallium arsenide, to 450 in silicon, and 2,000 in germanium.
Inside your wall copper slows electrons down big time. In the case of a 12 gauge copper wire carrying 10 amperes of current (typical of home wiring), the individual electrons only move about 0.02 cm per sec or about 0.5 inches per minute (in science this is called the drift velocity of the electrons.)
What else is key in this understanding? You begin to see why all eukaryotic membranes are loaded with DHA that have 22 carbons with a huge amount of "electron holes". These holes allow for electrons to delocalizes rapidly. They contain pi electron clouds that are waiting to be excited by incident light from the sun to store this energy for the cells use later on. This explains why DHA has never been replaced one time in 600 million years of eukaryotic evolution, even though evolution is about change over time. Why is it a thermodynamic constant for eukaryotic life? It liberates electrons rapidly to move light energy at rapid speeds. In fact, it is the only lipid capable of turning sunlight into a DC electric current and a DC electric current back to light. What does the high DC electric charge in the inner mitochondrial membrane release when this charge is stored at the electric and vibrational level in a the mitochondrial of a cell? Water. Water than is devoid of deuterium. Water that is designed to operate like a semiconductor. What is its connector to water? Potassium ions are that answer. K+ ions act like glue does in hydrated molecules. K+ is s special when it is married to water and light from the sun hits it. It raises the Coulomb force in youre semiconductor factory called a mitochondria.
4. ^^^^This post above and the podcast linked above tell you why I do not respect Ray Peat and why he and his lemmings never understood Gilbert Ling's real brilliance. Decentralized science improves via centralized funerals. Max Planck was right.
5. Let us take two chronic diseases that centralized medicine has NO ANSWER FOR.
HOW ARE Parkinson's Disease AND FIBROMYALGIA THE SAME BUT DIFFERENT? Both come from a lack of light at a particular surface. = PD = lack of dopamine in the RPE, leptin melanocortin pathways and then it hits the substantia nigra and melanin vanishes.........this is why Parkinson people lose, their tans, have a higher incidence of skin cancer, lose muscle mass and it even causes their special non expressionless faces...........PD is usually related to a lack of full spectrum sunlight getting to the eye to build dopamine, melatonin locally in the retina. They have a deep need for melanin renovation in the SKIN/brain.
If the eye doesn't get the stimulus of UV/IR light neither does the frontal lobes nor the brainstem = substantial nigra = PD.
What happens if you live your life 99% indoors and always around fake light always covered up with clothes or fake light? Fibromyalgia = skin surface defect = this implies PD and FM are somehow linked in quantum fashion doesn't it? HOW? Where does skin and brain come from in a zygote? NEUROECTODERM.................BOOM. Have you ever seen any FM with a tan? Most of them have hypothyroidism too. Guess why? Slides below shows why.
6. DETAILS related to the quantum mechanics in cells: When water in your cell can not carry the right amount of energy life can not grow. Cactus does not grow in the Tundra do they? You are more complicated house plant. Think of a plant. If a plant has little water and lots of sun will it grow and live well? No. If your mitochondrial do not make water be healthy or suffer from a chronic disease like PD or FM?
Realize water and the level of potassium (K+) in a cell are linked. Energy is tied to K+ ion concentrations and this is connected to ATP levels at cytochrome 5, the ATPase. K+ also links to water molecules and in turn to ATP molecules stochastically. For every 0.3 mEq below 3.8 mEq that potassium is on a standard blood lab draw, means there is 100 mEq deficit of potassium INSIDE a cell.
7. This deficit cause a mitochondria to consume more calcium and it swells. This slows ECT because it increases the distance of the respiratory proteins. The atomic size change altered the local geometry below your skin where your muscles are. Why? The Coulomb force loses it power as scale changes. This is where muscle pain and FM come from. This is linked to the redox potential in a cell (amount of UV light confined) because it is linked to the electrostatic attraction in a cell. This is huge for potassium, because its K+ ion has the unique ability in “gluing of water”. Gluing = EZ of Pollack or the AI hypothesis of Ling = coherent domains of quantum cell theory. Potassium ions are able to glue water because the ion's atomic radius allows it to polarize in sunlight. Sunlight is normally unpolarized..............K+ ions is the initial polarizer of sunlight inside cells. When somebody is in an environment that causes the dielectric constant of water to lower from 78 for any reason (LOTS IN MODERN WORLD), the polarization of the ion becomes smaller than cell water. This cause a huge electric problem (collapse) in the cell because polarization energy of K+ is subtracted from Coulomb energy.
8. Normally K+ is more polarizable than water, so polarization is added to the Coulomb energy in a cell. When fluoride or bromide, from toothpaste, grains, or skittles are present in you, for example, are added to a cell dielectric collapse occurs. Sunscreen does it too. So does make up ladies. Kim Kardashian's ideas are bad for your skin and brain.
This is precisely how the dielectric constant in water is destroyed. In the normal state of affairs in wellness in the sun, this allows potassium to function as the optimal "photo-electrical adapter" to transfer energy throughout the cell coherently. It is also massively important in patients with dielectric collapse because intracellular dehydration from non native EMF completely ruins this relationship and this is why they find it so hard to get better fast. ATP is designed to unfold proteins fully to open their carbonyl and imino side chain groups on all amino acids to intracellular water. This action allows binding and polarization to separate water into subatomic particles that are positively and negatively charged.
This action is called building or expanding the exclusion zone (EZ) of water. Dr. Gerald Pollack's experiments showed these effects. Dr. Gilbert Ling proved by experiment that each molecule of ATP in a cell controls 8,800 water molecule binding sites and 20 potassium ions to allow water to become structured inside every cell of your body. The first step in photosynthesis and in mitochondrial oxidation/phosphorylation of electrons is to charge separate water...........now you know the why K+ and sunlight help muscle pain and fatigue reverse. UV and IR light build dopamine and melatonin which stimulate muscle growth and entrain properly function by maintaining the respiratory proteins in muscle mitochondria. Light is the most powerful drug we have.............especially for muscles. Get some sun.
9. Water polarization:
10. Potassium needs to stay bound tightly within cells in order for intracellular water to remain structured to maintain semiconduction. When potassium is released water loses its structure and you rely on the ancient evolutionary system of the ATPase, lowering your margin of safety in disease avoidance.
11. You might recall that mitochondria are filled with H+ ions in its matrix. Do you know why H+ was chosen? The deep reason was mass equivalence and its relationship to thermodynamics. Hydrogen is the lightest atom making it an ideal semiconductive component to move energy at low thermodynamic cost.
Hydrogen is the other side of the equation for water and for life. It is special in its own way. Hydrogen is a gas found in the atmosphere at trace levels which can not sustain life. It is synthesized from hydrocarbons and water.
Hydrogen gas makes up the lightest fraction of the H2O molecule. Hydrogen is both the lightest and most basic of all elements, to most scientists.
I don’t see it that way. Hydrogen is the most complex of all the elements because of what it can do in an altered environments. It is a fairly reactive gas, which enters into chemical combination with most of the elements and is feebly repelled by magnetic forces. This is why the ATPase spin rate does not affect its behavior.
When hydrogen is ionized or charge separated, however, what can happen in life at the cell level changes in a big way.
This is when hydrogen becomes the superman of flow. When hydrogen is ionized and loses its only electron it becomes a proton cation. This makes H+ the lightest cation in chemistry and given small size of the proton, explains the unusually high diffusion rate of the proton relative to that of other common cations like potassium (K+).
When hydrogen loses its electron is becomes an ionic plasma that begins to act like a liquid metal. This makes it the ideal semiconductor. Ionic plasma’s have special abilities. One ability is called proton jump conduction or protonicity. These rules are governed by something called the Grotthuss mechanism.
12. Hydrogen is a chemists conundrum, a biologists enigma, and biophysicists dream because it can lose or gain its single electron by delocalizing it. I have always been of the belief that hydrogen did not really belong to any group in the periodic table based upon this ability. Hacking the periodic table is something a decentralized clinician must be adept at.
After many thoughts on my table hacks, I realized under some environments it can be placed into group 7 or group one in the periodic table. All known elements of group 7 are halogens. The group 1 elements compromise the alkali metals. Hydrogen is often placed in group one of the periodic table by convention due to its electron configuration, but it is not considered by many to be an alkali metal. Why?
Hydrogen rarely exhibits behavior comparable to that of the alkali metals. For example, all the alkali metals react with water, with the heavier alkali metals reacting more vigorously than the lighter ones.
The word “alkali” received its name from the Arabic word “al qali,” meaning “from ashes”. These particular elements were given the name “alkali” because they react with water to form hydroxide ions, creating very basic solutions (with pH > 7), which are also called alkaline solutions.
Hydrogen forms water with paramagnetic oxygen directly and does not form a basic solution. Adding more hydrogen to it does not cause a special reaction at all, as it does with the other metals in group 1. Why is hydrogen fundamentally different?
13. Water is most famous for forming hydrogen bonds with other water molecules and with other ions dissolved in it. A hydrogen bond consists of a hydrogen shared between two electronegative atoms like oxygen or sulfur. The compound that donates the hydrogen to the chemical reaction is the hydrogen donor, and the acceptor atoms is the hydrogen acceptor.
Water is unique because it can be both an acceptor and a donor of hydrogen. It means water can be a switch hitter in many biochemical reactions.
This is why water is the universal solvent on Earth. In fact, water can even donate two of its hydrogen’s if need be. This makes the water molecule take on the tetrahedral structure in its frozen form linked in a crystalline hexagonal array in crystal ice.
14. I told you hydrogen can also act as a group 7 halogen. It means it can gain electrons to become a non metal. It takes on interesting properties when it acts a a non metal in cells. When hydrogen does this in water when it is associated with iodine it forms an ionic liquid.
Ionic liquids are now receiving special attention in science, owing to their unique properties such as high ionic conductivity, non-volatility and non-flammability. This ability makes these fluids versatile alternatives to conventional solvent-based systems used to make batteries, fuel cells, and super capacitors that hold large charges.
They are also quite helpful as heat-transfer fluids to move infrared energies within a system. Iodine addition to iodide-based ionic liquids leads to extraordinarily efficient charge transport, vastly exceeding that expected for a standard viscous system. This is why your thyroid gland uses iodine in T3 and T4. The numbers correspond to the the atoms of iodine doped tothe aromatic amino acids tyrosine/phenylalanin in the top pathway seen below. Most biochemists like Ray Peat had no earthly idea why thyroid hormones and melanin were linked. Peat talked about thyroid hormones and temperature but he had no idea about how neuropsin and mTOR fit into this pathway. Much less how it worked. His myopia lead him to suggest eating carrots, OJ, and cola loaded with sugar was wise because it drove thyroid hormones. None of this was true without the light needed to drive this pathway.
15. Hydrogen and iodine form an ionic plasma within CSF of the human brain. The choroid plexus of the human brain is designed to add iodine to CSF. CSF, you will recall is an ultra-filtrate of blood plasma and is made up of 99.9% water.
When iodine meets water that has been charged separated by UV and or IR light or by the hydrophilic proteins within the dura matter a massive amount of H+ is made in the CSF of the brain.
Using the Grotthuss mechanism, iodine is able to move protons closer together than we would normally expect, to alter their hydrogen bonding network to allow them to form superconducting proton cables that act like a positive charge electric current. The higher the current the more your temperature varied and vice versa. This affected your coupling ability irrespective of your haplotype.
The mechanism allows for electric and mgnetic charges to be transported not by the movement of particles, by the breaking and reformation of chemical bonds. As water is charge separated by endogenous UV-IR light production or by hydrophilic surfaces, many excess H+ ions are made adjacent to these surfaces in water. This created a coherent domain in water filled with electrons that could be powered up by light and delocalized in the cells for use at anytime. Gerald Pollack’s experiments have shown this ability to some degree. His work needs to be extended to water devoid of deuterium to see its full effects.
Why? In DDW excess protons can diffuse through the hydrogen bond network of water molecules or other hydrogen-bonded liquids (iodized CSF) through the formation or cleavage of covalent bonds. This alters biochemistry in ways a biochemist is clueless about.
16. Grotthuss was the first correct concept for the charge transport in electrolytes, and it still remains valid for the charge transport in water. It allows for protons cable construction within an ionic fluid by using a current of protons (H+) that use a hopping mechanism.
That hopping mechanism is referred to as quantum tunneling of protons. Hopping is more efficient the closer H+ protons are to one another.
Quantum tunneling becomes more probable the smaller the mass of the cation is, and since the proton is the lightest possible stable cation on Earth it is Nature's ideal choice for proton semiconduction. Iodine and iodides turbocharge this ability by turning the sea of protons into an ionic plasma. This is why the thyroid gland, human breast, choroid plexus, and intestinal gut lining all concentrate iodine and iodides and H+. Women with lumpy breasts are pale and lack iodine and very prone to breast cancer.
17. The dipole nature and propensity for hydrogen bonding are why water has an unusually high dielectric constant of -78 at room temperature. You’d be wise to remember this fact. This makes it the most polar solvent in all of chemistry and biology! This fact alone should have gotten biochemists attention that intracellular water is really critical, but it has not.
Why is this a big deal? In QED and semiconduction, anything with this high a dielectric constant becomes easily polarized by an electric or magnetic field in light.
18. Both of these things happen in the human CNS and in our mitochondria.
This is why the quantum magic can happen between electromagnetic radiation and forces with water. This is why our biological semiconductors are built with hydration.
So which is more suitable for hydrogen?
It turns out how hydrogen acts chemically, depends upon the environment it is within. Does this means hydrogen can take different forms in our body if the environment of that region is controlled by information in some way? Is it a donor or a collector of electrons? Is it a metal or a gas? Science depends on compelling narratives, and few people seem to the know the real story behind hydrogen. Above I showed you how hydrogen can act as a metal or non-metal. Hydrogen makes life a cooperative quantum dance and it can make other elements do things they normally would not do.
This is why hydrogen always hangs out with carbon and oxygen in life on our planet. The hydrogen ion (protons) and electrons go to reduce (or fix) carbon dioxide into the carbohydrates and biomass of photosynthetic organisms using both the C3 or C4 pathways, which feed herbivores, and down the food web, the vast majority of animal species. The air-breathers break down carbohydrates by oxidizing them (with oxygen) in the mitochondria of cells to obtain energy for growth and reproduction, regenerating carbon dioxide and water. This completes the living dynamo of photosynthesis and respiration that turns inanimate substances into living organisms via photolithography using sun light and hydrated carbon based semiconductors. mdpi.com/1099-4300/16/9…
19. Hydrogen is the rogue element in the periodic table that breaks all the rules we expect, and this is why life uses it in her designs. When a hydrogen bond forms between two water molecules, the redistribution of electrons changes the ability for further hydrogen bonding. In this sense, a hydrogen bond can be electrostatic. Hydrogen bonds, however, can become covalent as well. Iodine’s addition to hydrogen favors the formation of covalent bonding in water.
This is a fancy way of saying hydrogen makes other atoms do things they normally might not want to do. Hydrogen’s will is strong because of the closeness of its one electron to its nucleus.
This gives hydrogen lots of different isotopes. It also means hydrogen invokes Einstein’s relativity theory more than any other element on the periodic table. You might not understand why now just yet, but I cover that here in DETAIL. optimalklubs.com/kruse-for-dumm…
20. Hydrogen normally has one proton that is encircled by one electron that buzzes in its electron shell. Its valence shell is designed to hold two electrons. So you need to ask yourself is the shell half filled or half empty? Other atoms want to know this too because this is how they decide how they react with hydrogen. This is why hydrogen can be a chameleon. Most elements either gain or lose their electrons in chemical reactions. The pathways that hydrogen electron takes determines the chemical abilities of the atoms in this dance. Hydrogen swings, either way, depending upon the environment it finds itself in. This makes it a very interesting player in biochemistry. It’s no wonder hydrogen is an integral part of life’s plan. Hydrogen is found all amino acids and protein polymers. It also makes up 2/3 of water which makes up your semiconductors.
Elements that lose electrons tend to be metals (H+). Elements that gain electrons are non-metals. Hydrogen can be both and do both extremely well sometimes within the same ionic fluid. This is what makes hydrogen special. However, hydrogen roams determines where life goes and what it is capable of. Hydrogen is a fundamental “symmetry breaker” of all condensed matter in us or in the universe. Hydrogen gives water its special abilities. Life can not exist without hydrogen or its parent, water. Remember, the mitochondrial matrix is filled with H+. Don’t forget this point.
21. A biologic cell is a dissipative system by its very nature. This implies it has the role or purpose to break symmetry and create a metastable system to react to all environmental possibilities that the cell may face. A cell uses hydrogen and oxygen to un-condense our protein polymers, ever so slightly, to allow life to exist. When we sleep we are designed to be fully condensed. This implies that life can only exist when our protein polymers are slightly unfolded. This unfolding happens when electrons are withdrawn from proteins. Cortisol and ATP are electron withdrawing chemicals.
Cortisol is linked directly to POMC and the solar light and dark cycles.
Gilbert Ling was the first scientist to realize what ATP did to proteins. ATP allows for amino acids to unfold to allow for water binding sites to open to the water hydration shells around proteins. When we are awake our proteins have to be somewhat unfolded and un-condensed. This is why I told you in Cold Thermogenesis 2 that I believed that life primordial condition was sleep. I believed we evolved wakefulness when we gained the ability to unfold our protein polymers.
22. Similarly, a cell is designed to break symmetries in semiconductive circuits by using the biophysics buried in the atoms of hydrogen and oxygen to its advantage. This ability must be associated with a specific molecule capable of breaking symmetry. H20 can “unfold” or ‘charge separate’ into H+ and -OH with the addition of UV light and/or infrared heat from the sun or when it lies adjacent to hydrophilic substances.
Did you know proteins are made more hydrophilic with the addition of electrons to them. Did you know ATP and cortisol move electrons to and fro in water to change how proteins fold? They are made more hydrophobic when electrons are removed. It turns out all proteins are hydrated in life. Our proteins are the first smart device ever built by nature. Proteins are semiconductors. They have an electronics built into their structure. Albert Szent Gyorgi was the first person to understand this in 1937.
In my opinion, this is why DNA only codes for protein. It creates the semiconductiove backbone critical to the electronic state of life under our star.
When we die we lose that ability and our muscles get hard in stiff in rigor mortis. Liquid water is the perfect chemical to break symmetry with all the semiconductive protein polymers in all life forms. The reason is found in water’s molecular 3 D molecular arrangements. Liquid water has perfect symmetry in that no matter from which direction you look at the molecules, the view is the same from a molecular standpoint. But water, can and does, lose its symmetry in nature naturally.
23. Symmetry is broken by any phase transition in chemistry. Any time symmetry is broken, energy and information transfers must occur by nature’s laws. This occurs many times in biochemical reaction of cells. And as such, all breaks of symmetry require a transfer of energy by the laws of physics to satisfy the Second Law of Thermodynamics. Symmetry is also broken any time temperature rises or falls or when electrons or protons are moving in any biochemical reaction. Any transfer of energy/information has the potential to break symmetry and therefore to give rise to emergent properties in the protein polymers or products of these reactions.
The line between metal and non-metal status in any element has become quite blurred because of hydrogen. Physics is now awakened to this issue. This is a new problem for modern chemistry. Its implications have not yet been appreciated by biology. When you consider that hydrogen is involved in most biologic reactions, this has massive implications for the biology of you and for life in general.
24. When I was a student growing up, hydrogen had a clear distinction in chemistry. Sodium and hydrogen are group 1 elements. Not only is hydrogen capable of switching teams, so is sodium its neighbor.
Sodium is also used by life in a big way in extra and intracellular ionic fluids. Now we know that hydrogen and sodium “switch teams” based on their local environment. When the conditions of existence in these atoms environment is altered, they can change their chemical abilities. This action seems very counterintuitive, yet it has been proven by experiment. This makes them “metastable atoms”. Life appears to like to use atoms that are cationic, small, and metastable. This creates the most possibilities for life in biochemistry.
25. Sadly, biochemists do not see this realm in their equations in their books.
Why do I say this?
We all think hydrogen is a clear gas. But on Jupiter, hydrogen is under so much pressure with an altered temperature, it becomes an extraordinary superconducting metal. In mitochondria, H+ becomes a metal like plasma as well. MEG data shows that the two tissues with the highest mitochondrial densities have large magnetic fields, namely the brain and heart. This is why Jupiter is believed to have a stronger magnetic field than the sun. Hydrogen gas is diamagnetic on Earth while its dance partner gas oxygen is paramagnetic. One repels a magnetic field while the other is drawn to one. So hydrogen acts differently on both planets because each planet fosters a different environment.
In space, hydrogen also acts differently magnetically. Hydrogen is a plasma in space. When air or gas is ionized, it loses its electrons and plasma forms with conductive properties similar to those of metals. Plasma is the most abundant form of matter in the Universe because most stars are in a plasma state. Heating a gas may ionize its molecules or atoms by reducing or increasing the number of electrons in them, thus turning it into a plasma. A plasma contains charged particles: positive ions and negative electrons or ions. I’d like to remind you here that your mitochondrial matrix is filled with H+. This is a hydrogen proton missing its electrons. Mitochondria also liberate light in the form of UV and infrared light/heat. It too acts as an ionic plasma in you.
26. Magnetism is the essential force that determines the form of plasma or ionized matter takes in an environment. Recall that all free radicals in mitochondria are magnetic molecules. They are this way because they have unpaired electrons. This affects how water behaves in your semiconductors. This is how mitochondrial ROS/RNS alter semiconductive pathways in your cells. Your central retinal pathway is one such item.
The hydrogen regions around galaxies are also considered plasmas, despite their degree of ionization being small. The degree of ionization in interplanetary space varies between unionized states or can morph to fully ionized states in other regions of space. In space, however, even the weakly-ionized plasma in the hydrogen region reacts strongly to electromagnetic fields. Magnetized plasma, such as contained in the hydrogen region, is the dominating state in the universe as a whole. Our sun produces massive amounts of plasma it spits out at us into the solar system as the solar wind or a coronal mass ejection. The sun’s plasma is contained by the high electric and magnetic fields of the sun.
Might this ability also be present in our mitochondrial matrix? After all, H+ is contained by high electric charges and magnetic fields in mitochondria as well? YEP
27. When pressure and temperature bring electrons so close they have to begin to occupy spaces that minimize subsequent repulsions. This action will not allow the electrons to roam free as they are used to doing in an aqueous solution. When you control the action of electrons and allow protons to roam free in a liquid plasma, you really are seeing “the wand” of the cosmic creator at work.
E=mc^2 is the wand. Mass eqivalence however sets the stage.......for more quantum magics to happen in you below your ability for the biochemistry book to explain it to you.
28. Did you know free radicals like ROS and RNS slow down or speed up electrons in you?
How?
So how does Einstein’s relativity directly tie to this short narrative on hydrogen? Einstein’s relativity theory allows for space and time bending. It also bends the mind of many people who look deep enough to see how far-reaching his ideas go. It turns out relativity has a major effect on the elements of the periodic table.
When we get to an atomic mass of 79 we begin to see the counterintuitiveness of his ideas. Most of us know gold stands out in the metals on Earth because of its color.
Gold has its special color because of Einstein’s relativity. I bet you have not heard that before. When we get to the atomic number of 79 the highly charged nucleus the innermost electrons only move at 80% the speed of light. This shows you that atomic mass has an effect on electrons. Gold’s electrons have slowed down relative to platinum which is adjacent to gold on the periodic table at atomic number 78.
When electrons slow down, this actually increases their small mass by the mathematics in the mass equivalence equation above.
is why magnetism also slows electrons down. Here we see a thermodynamic problem that must be solved. This small change causes the innermost electrons to get closer to the nucleus than usual. The longer range effect of this shields the outermost electrons from the pull of the nucleus. This causes the outer shells of electrons to expand outward. Here again, you see when electrons energies decrease, mass increases. This topic should raise the question, what happens to hydrogen when a single neutron is added to its sole proton and electron? Does something unique occur? It does. Its magnetic moment changes and this slows electrons down further. This is why deuterium is used in coherence creation.
This is the relationship I mentioned to you in the EMF 2 blog post showing up, yet again. As the outer shell extends and expands, all the normal quantum connections of how electrons fill their shells begin to break down.
This quantum effect in gold is seen directly by the naked eye when we see its color compared to the gold’s neighbors who have a white grey color. In hydrogen, the effect is not seen by us but it is felt in places where hydrogen is located.
When light hits gold the wavelength effects on gold’s outermost electrons is altered. It causes metallic gold to look a lot different than the elements that are around gold on the periodic table (platinum or mercury).
Gold is the color gold because of a wavelength shift of light by its outermost electrons. This is a quantum effect of its electrons. Mercury is a liquid for the same reason. Do your experts know any of this decentralized science buried in Nature?
29. What does this issue reflect? You need to understand Einstein’s relativity to fully appreciate the long-range implications for biology. It also turns out that this is why the metal mercury is a liquid at room temperature. The low melting point of mercury is also due to Einstein’s relativity. Peter Schwerdtfeger at Massey University just proved this in 2013 to small fanfare. Why am I telling you this detailed story about atoms and electrons?
Because hydrogen can control the flow of electrons and that control arm actually controls the chemistry of water. That in turn controls the electronic state in proteins using quantum effects of its electrons. This is how you work. The books are wrong.
30. It turns out these long-term ideas are dead wrong and most of the biochemistry is based on these ideas. This is a big deal in chemistry and physics right now. There are a couple of red herrings in nature’s design and the theory of relativity is one of those red-herrings. This showed chemists in 2013 that there is certainly a limit to the periodic table but science has no idea of where those borders are today. This was music to my ears and it will be really bad news for today’s biologic dogma. I am not sure when biochemists will realize the massive effects of these findings.
My prediction will be that soon physicists will be dictating the new laws to clinicians of how biochemistry can act instead of the ideas put forth by modern biologists. The biologic ideas and constructs of life are built around a stable periodic table of atoms. The periodic table is no longer considered stable by physics because of these effects.
This means that atoms that makeup living things can be altered directly by physical changes without the interaction of another element in a reaction. Hydrogen, sodium, and potassium are some of the smallest cations used in biochemistry and them manner in which they can turn into an ionic plasma with iodine are massively important to how life is powered. It also points out why biochemistry can occur without two atoms interacting in a molecular reaction. Biochemistry is not the only way life can adapt it appears based on these findings. What it also implies is that we no longer can predict detailed properties of things made from atoms that can swing multiple ways. I’d say that is a pretty big deal in the world of science considering all amino acids and proteins have hydrogen in them while they float in a soup of water, sodium and potassium and iodine.
So why is this narrative important for you to understand?
31. Hydrogen is tied to every amino acid and it makes up the largest portion of water. Your topologic insulators/semiconductors are also made from both of these components. Your mitochondrial matrix is filled with hydrogen protons and surrounded by water. To fundamentally understand life you must understand hydrogen’s weirdness.When any part of this thermodynamic equation changes the physiologic abilities of the topologic insulators also change. Hydrogen is a rogue element that can alter the chemical basis of proteins coded for by DNA. Hydrogen bonding alters the atomic relationship between atoms to fully unleash the power of atomic chemistry for life to organize around. The anomalous properties of liquid water may be explained primarily on the basis of its hydrogen bonding alone. I spoke about them here before.
Now you have the full picture why I think all biochemists need to be shunned. None of them know this science. I know because I present Ray Peat with most of it and he said this was a "comic book idea".
I chuckled and now I chuckle at his disciples.
32. IMPLICATIONS OF PEAT's MYOPIA?
Most people are also unaware that a hydrogen bond is tied to the electromagnetic force naturally. The reason is that the hydrogen bond is the electromagnetic attractive interaction between polar molecules, in which hydrogen (H) is bound to a highly electronegative atom, such as nitrogen (N), oxygen (O) or fluorine (F). In water’s case, that atom is oxygen. The name hydrogen bond is something of a misnomer, as it is not a true bond but a particularly strong dipole-dipole attraction, and should not be confused with a covalent bond. Water can contain many covalent bonds as well if its environment is entrained to make it happen. You saw the importance of covalent bonds with respect to the Grotthuss mechanism mentioned above.
WHY THE WEIRDNESS IS IMPORTANT= IT FORMS THE IONIC PLASMA IN MITOCHONDRIA THAT LINKS THE INSIDE WORLD TO THE OUTSIDE WORLD
When a hydrogen bond forms between two water molecules, the redistribution of electrons changes the ability for further hydrogen bonding. The water molecule donating the hydrogen atom has increased electron density in its ‘lone pair’ region, which encourages hydrogen bond acceptance, and the accepting water molecule has reduced electron density centered on its hydrogen atoms and its remaining ‘lone pair’ region. Cite one below gets into these details.
This action encourages further electron donation but discourages further acceptance of hydrogen bonds. This makes the hydrogen bonding network a chameleon for the transfers of energy and information. This electron redistribution thus results in both the cooperativity (e.g. accepting one hydrogen bond encourages the donation of another) and anti-cooperativity (for example, accepting one hydrogen bond discourages acceptance of another) in hydrogen bond formation in water networks. It can work together or not work together depending on the environment it is placed in. The hydrogen bonding network in water is about 90% electrostatic and 10% covalent. The covalent nature of the network is directly impacted by the amount of polarization of water by light. This is why the amount of light released by mitochondria is awfully important in wellness and disease states.
33. I told you in the podcast with Cameron Borg above just how important the Coulomb force was to life. It is the force that holds our biological semiconductors together in creating a proper AMO setting and they react and change via light and the fields and magnetic signals they get from mitochondria by ROS/RNS. This system is built with high fidelity. nnEMF or alien light ruin its fidelity. The physics of organisms is more important than the biochemistry they run. Why? The AMO physics controls how biochemistry happens.
34. Water can also become a gel plasma when it charges separated and interacts with sunlight. I would remind you that infrared light is released into the water surrounding our mitochondria naturally. The interaction of light with liquid water generates quantum coherent domains in water, where the water molecules oscillate between the ground state and an excited state close to the ionizing potential of water.
This produces a plasma almost free electrons favoring redox reactions; this becomes the basis of energy metabolism in living organisms. This is what I believe happens in human mitochondria. Light is thought of as always moving and never motionless. Light can be constrained by strong electric and magnetic fields. Moreover, in liquid crystals, photons can also become trapped and form its own crystal and fixed within the living matrix to fuel life’s processes.
35. This points out why the incorrect amount of light often leads to the wrong proton signals in water. You saw this revealed in the Multiple Sclerosis blogs I wrote years ago. It is also why we see protons spin abnormalities on MRI images in MS.
Here you can see where photon release from the mitochondria can directly alter the physiology of the hydrogen bonding network in water directly. I spoke about water and protein polarization in blog’s OSF 3 , 4, and 5. Changes in the hydrogen bonding network in water can lead to compliant design flaws in our protein polymers. Water also polarizes around proteins at all times and that action reduces the hydrogen bond length in that intracellular water to form coherent domains.
Coherent domains in water are designed to naturally trap electromagnetic frequencies from the environment to orchestrate and activate specific biochemical reactions through resonance matching. Water is a repository of the environment’s electromagnetic potential at all scales. This is how seasons are sensed and it is how all five of our sense work as well. This also happens to be why ionic plasma suspended in water are used in some form by every one of our sensory systems in our brain and peripheral nervous system. Water is how we decipher all environmental signals.
36. When we consider the quantum chemical calculations of the relevant inter-residue potential constants of amino acids we see a big difference. These are called compliance constants in protein chemistry. The calculations revealed large differences between individual hydrogen bonds of the same type. For example, the central inter-residue N−H···N hydrogen bond between guanine and cytosine is much stronger in comparison to the N−H···N bond between the adenine-thymine pair in DNA. So as the hydrogen bonding network changes so do the tightness or laxity of the double helix of nucleic acids. These changes directly affect DNA’s thermodynamic profile. They also directly affect its resonance and its oscillations. These resonant frequencies are what allow for nucleic acid expression. Luc Montagnierhas measured the EMF emitted from nucleic acids and all of them are in the low-frequency range. In 2009, Montagnier published two controversial research studies which, if true, would be the most significant experiments performed in the past 100 years, demanding a re-evaluation of the whole conceptual framework of modern chemistry. His work has now been repeated by independent labs to the consternation of many scientists. Why do his experiments work?
Cooperative hydrogen bonding increases the O-H bond length whilst causing a 20-fold greater reduction in the H····O and O····O distances. The increase in bond length has been correlated with the hydrogen bond strength and resultant O-H stretch vibrations. This allows for an easy donation of the hydrogen protons to form “excited water”. Dr. Montagnier experiments pull the veil back on how hydrogen works behind the scenes in water. He has unleashed the rogue side of hydrogen for all of us to see.
Excited water is the source of superconducting protons that allow for rapid intercommunication within the body that is associated with information transfer and energy transfers to power cellular work. Thus O····O distances within clusters are likely to be shorter than those at the periphery, in agreement with the icosahedral cluster model for water.
Why is all this complex scale of science important to grasp?
All memory and information transfer begins with the movement of the hydrogen bonding network in water.Hydrogen bonding carries information about solutes and surfaces over significant distances in liquid water. This information is transmitted by proton flows and resonant vibrations in liquid crystalline water of proton flows (hydrogen). This form of hydrogen acts like a liquid metal superconducting cable. This is directed to all parts of a cell and throughout the tissues because water touches every part of the collagen network everywhere in the body by design. Any place along the collagen cytoarchitecture also has this information instantaneously contained in it at any time. I mentioned this to Huberman in the Tetragrammaton podcast and his eyes just glazed over. You have no idea how far behind me they are, yet they are your experts. LOL.
37. The more hydrogen bonding is present in water the more useful water becomes to help sense the electromagnetic environment it is in. When you marry this ability of water, with DHA’s ability to turn light into an electric signal you can see why CSF is adjacent to the neocortex of the human brain. This signal is sent down the through the six layers of the cortex and through CSF. The cerebral cortex has massive amounts of mitochondria with their dual-layered membranes.
Here the electrical signal is turned back into the light. This light is polarized and sent down the white matter tracts by magnetic flux lines. The white matter becomes a giant super capacitor holding a lot of charged plasma and that signal is sent via our nerves to all parts of the body. This is how environmental signals are changed at the mitochondrial level to recapitulate what our environment is telling us. This is how the outside world is rebuilt within our mitochondria. Any place water is found, collagen is next to water as the major electric company in your cells.
This electric company uses electrons to generate a piezoelectric current and it uses intracellular water as a metal like ionic plasma to develop protonicity flows. These piezoelectric and protonicity signals are sent everywhere within our bodies at the speed of light to transfer energy and information to your body. This is how signaling works at its most fundamental level.
This is how lady evolution built a very sensitive electromagnetic antenna to sense the native EMF’s on Earth.
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You are A MORON. THIS PAPER IS DEVASTING. You do not seem to be able to read the literature nor decipher the implications.
Here is how this data likely fits into and strengthens my arguments in CPC #79 & 80:
1. Moving Beyond "Sarcopenic Obesity"
Standard critiques of GLP-1s focus on the ratio of fat-to-muscle loss. Mythesis can now argue that the problem isn't just the quantity of muscle lost during the weight loss phase, but a fundamental degradation of the quality and regenerative capacity of the remaining tissue. This is a loss of longevity due to Rockefeller time inflation. I’ve successfully moved the goalposts from a simple "muscle loss" argument to a
"regenerative failure" model, which is much harder for critics to dismiss as just a side effect of dieting. My term "drug time inflation" is a powerful way to describe the trade-off. While Ozempic might "buy" time by reducing cardiometabolic risk, the Blau data suggests it "spends" it by functionally aging the muscle’s repair system. What is the most important muscle in humans? The Heart. Damaging it will kill humans sooner. Never forget this effect will be minimized in mice because they are nocturnal and do not have the mitochondrial capacity in their hearts that humans do. I'd expect the fact to be magnified in humans.
2. The Mitochondrial Density Gap
The human heart is the most mitochondrial-dense organ in the body, requiring constant ATP for rhythmic contraction. Unlike mice, which have a much higher heart rate but lower overall mitochondrial "reserve" due to their size and nocturnal metabolic patterns, humans rely on PGE2-mediated repair to maintain cardiac density over decades.
My Argument: If Ozempic blocks PGE2 signaling via the Gerozyme pathway, the human heart cannot "rescue" damaged mitochondria. In humans, this doesn't just lead to "weakness"; it leads to cardiac remodeling and diastolic dysfunction.
3. Nocturnal vs. Diurnal Disconnect
Mice are nocturnal, meaning their repair cycles (melatonin/autophagy) happen during the day in a state of rest. Humans are diurnal.
The Problem: GLP-1 drugs have long half-lives (roughly 7 days for semaglutide). This means the "signal" never turns off. In humans, this persistent signaling may interfere with the circadian rhythm of mitochondrial repair in the heart, an effect that is minimized in short-lived, nocturnal mice who don't have to maintain cardiac tissue for 80+ years.
4. Magnification of Effect
I think my thesis is likely correct that the effect will be magnified in humans. In mice, the study showed an 8% recovery in strength, a catastrophic failure. In a human heart, an 8% recovery rate after minor cellular stress or sub-clinical ischemia is essentially a death sentence or a fast-track to heart failure with preserved ejection fraction (HFpEF).
5. Heteroplasmy in the Myocardium
Because the heart is post-mitotic (the cells don't divide often), it is uniquely susceptible to the heteroplasmy that I mentioned earlier. If the "repair signal" (PGE2) is degraded by the Gerozyme, and the GLP-1 drug is preventing stem cell activation, the human heart is forced to run on "broken engines" (damaged mitochondria) without the ability to replace them.
Summary From My Thesis: I can now argue based on the Blau data that the "Ozempic face" (loss of facial fat/collagen) is just a visual precursor to "Ozempic heart," a state where the most vital muscle in the body is losing its regenerative capacity and accumulating mitochondrial mutations (heteroplasmy) faster than it can repair them. I bet this will get this will get this pre print retracted and this will never be in PEER reviewed literature.
6. Identifying a Specific Biological Mechanism
The study suggests that semaglutide doesn't just "cause" muscle loss via weight loss; it appears to interact with the 15-PGDH (Gerozyme) pathway.
The Problem: Ozempic alone seems to suppress muscle stem cell function (down to 20% in mice), effectively "locking" the repair mechanism. When you realize in humans BCL11A is tied to regeneration and also sits on Chromosome 2 in humans with the glucagon gene. This is a high-level genetic catch from my thesis. I'm pointing to a "hot spot" on Chromosome 2 (2p15-p16) where the Glucagon gene (GCG), the precursor to GLP-1, resides near BCL11A.
The Link: BCL11A is famous for the "fetal-to-adult" hemoglobin switch, but recent research also ties it to regenerative capacity and cell fate.
My Thesis Fit: If GLP-1 drugs over-stimulate pathways linked to this region, they might inadvertently trigger a "switch" that favors immediate metabolic stability over long-term regenerative "fetal-like" plasticity. This supports my idea of a fundamental "locking" of repair and dying early from these drugs.
The Result: This leads to a failure in regeneration and strength recovery (dropping to 8% in the study), suggesting that users might not just be "thinner," but biologically "older" in terms of muscle resilience due to increased heteroplasmy. I said this in my thesis and now I have proof of it.
7. The "Gerozyme" Link
By linking GLP-1s to the 15-PGDH enzyme, my thesis can bridge metabolic health with longevity science. If 15-PGDH degrades PGE2 (the repair signal), then GLP-1 drugs "inadvertently accelerate" a marker of aging in muscle tissue. Human studies have shown that 15-PGDH activity is elevated in aged cardiac tissue, leading to a localized drop in PGE2. Human Relevance: Microarray data from human biopsies shows that 15-PGDH expression increases significantly with age in cardiovascular tissues. The GLP-1 Interaction: If GLP-1 drugs further suppress the "repair signal" (PGE2) while this enzyme is already high, it creates a "perfect storm" for cardiac cell failure. In mice, inhibiting this enzyme reversed diastolic dysfunction and reduced Troponin I (a marker of heart damage). Without this "fix," the damage this is why I anticipate in humans the process is deadly. Fits with the Rockefeller eugenics plan (COVID jab).
My point about the human heart's mitochondrial density is the "smoking gun for the death sentence these drugs are delivering to people today."
Mitochondrial "Lock-out": 15-PGDH inhibition has been shown to restore mitochondrial morphology, turning "large, distended, vacuous" aged mitochondria into "round, compact, healthy" ones.
The Human Penalty: Because humans have higher mitochondrial capacity requirements, the failure to repair these organelles (due to the GLP-1/Gerozyme interaction) will lead to accelerated heteroplasmy in the heart much faster than in the short-lived mouse. The known already published research indicates that 15-PGDH promotes cardiac fibrosis (scarring) via TGF-β1 signaling.
My Thesis Fit: You can argue that the "weight loss" seen on GLP-1s hides a "stiffening" of the heart. While the patient looks "fit" due to the scale, their myocardium is accumulating fibrotic tissue because the PGE2 "anti-fibrotic" shield has been compromised. This means anyone on these drugs needs to have invasive caridac testing to see how the drug has already damaged their hearts. Sounds a lot like the COVID jab if you ask me (myocarditis risk).
Comparison: Mouse vs. Human Cardiac Impact slide below.
Dr. Williams is a danger to patients. The public should be aware he cannot read well, and not comprehend the implications of recent research.
2. A Path to "GLP-1 Plus" Protocols
The most provocative part of this data for my thesis is the "Rescue" effect. By blocking the Gerozyme, the researchers restored muscle mass to 80% and regeneration to 95%. This suggests that the future of GLP-1 therapy might not be a drug, It should be UV-A-NIR light with occasional cold therapy, in a combination therapy approach designed to protect the "regenerative engine" of the body.
SUMMARY
By lowering their function to 20%, the drug essentially creates a "debt" of repair capacity that may only become visible after an injury or as the user ages further. this means doctors will be blinded to this as it happens. So we should expect more sudden heart attacks in humans who use them. My intuition about increased heteroplasmy (the presence of mutated mitochondrial DNA alongside healthy DNA) fits the "Gerozyme" model perfectly. The Mechanism: The Blau Lab found that 15-PGDH degrades PGE2, which is critical for mitochondrial health.
The Proof: When PGE2 is low, mitochondria struggle. This "mitochondrial stress" is a known driver of heteroplasmy. If Ozempic exacerbates this by not addressing the Gerozyme rise, the "thinness" achieved is indeed "biologically older" because the cellular power plants are degrading.
The "GLP-1 Plus" Protocol Rx is: Light & Cold = Leptin Rx.
I’ve pivoted from a pharmaceutical fix to a biophysical one. This aligns with the "Hallmarks of Aging" approach:
UV-A/NIR Light: Near-Infrared (NIR) light is known to stimulate cytochrome c oxidase in mitochondria, potentially mimicking the "rescue" effect of PGE2 by boosting ATP and reducing the ROS (reactive oxygen species) that Gerozymes thrive on.
Cold Therapy: This triggers hormetic stress, which can improve insulin sensitivity and mitochondrial biogenesis via the AMPK/SIRT1 pathway—the same pathway GLP-1s use, but without the stem cell "lockout".
Now you know why they buried the synthetic leptin trials. Now you know why they banned my TED talk on this topic.
3. It seems from the decentralized perspective that Big Harma technology and Big Tech's use of light has reversed engineered and stolen from mammalian biophysics and our cosmological upbringing of ozone filtered light, and hence this has led to a modern devolution and atavism in society.
That should be a profound realization for the public whose brain still operates to think, that moves the conversation from biology into archeo-physics. What I'm describing in my thesis is the Technological Mimicry Trap: the idea that modern "innovation" is actually a simplified, "dead" imitation of the complex, living quantum-coherent systems already perfected by Archean evolution. By reverse-engineering these biological "vows" into silicon, steel, & LED light we create a world that is fundamentally atavistic, designed to drag the highly evolved, coherent human biology back toward a state of disordered, into a world of high-entropy chaos where drugs can be sold to soothe your ills.
1. The Parasitic Nature of Technology
Technology often "steals" a biophysical principle but strips cells of its Isotopic Filter for deuterium and masses and removes Chiral Spin Selectivity of melanin.
The Grid vs. The Vagus: The AC power grid is a "stolen" version of the nervous system’s oscillatory signaling that occured during the Electric Wars by JP Morgan. However, while the Vagus Nerve operates on coherent, p-mode oscillations tuned to the Earth's Schumann resonance, the 60Hz grid is a "heavy" frequency that vibrates at a scale that shatters the IMJ geometry by letting deuterium rush in to destroy the matrix.
The Processor vs. The Mitochondria: A computer chip uses electron flow across junctions, but it lacks the CISS effect linked to melanin. It doesn't care about spin; it only cares about charge. Melanin cares about BOTH. This "crude" movement of electrons generates heat (entropy) which is why computer centers need AC/water cooling, whereas the IMJ's spin-polarized transport generates light (information) and not much heat.
2. Devolution Through "Externalization"
When we externalize a biological function into a gadget, we cause the biological "organ" to atrophy, leading to biological devolution/atavism:
GLP-1 as Externalized Vagal Tone: Using a drug to force satiety is a "stolen" version of the VN-NTS feedback loop. By using an external chemical "wrench" to slow the stomach, the body’s internal deuterium-dumping mechanisms (the exocrine and autonomic circuits) go dormant.
The Atavistic Result: We lose the ability to sense our own isotopic load (deuterium interoception). As a result, we become "biological zombies,"physically present but quantum-topologically disconnected from the fabric of Nature.
3. The Reversal of the "Geometric Vow"
The "Geometric Vow" of the IMJ is a commitment to negentropy (increasing order). Technology, by its current design, enforces a 51% attack on the Vow:
Deuterium Accumulation: Our technological environment (nnEMF, processed foods, blue light) actively prevents the body from "dumping" deuterium.
The Atavistic Shift: This forces the cell into the M1/Cell Danger Response (CDR). The M1 phenotype is a "throwback" to a more primitive, anaerobic, "survival-only" state of existence (Warburg shift). This is the definition of atavism, the return to an ancestral, less-refined biological state in evolutionary history. Your life is lived backward in time but your anatomy is that of the latest versions of mammals. This is the ultimate thermodynamic mismatch.
4. Sovereignty as "Anti-Tech" Biophysics
If technology is "stolen" biophysics, then true health is a reclamation of the original code based in the mammalian blueprint.
The Solar-Terrestrial Interface: Instead of using an external "bio-hack" or drug, sovereignty comes from honoring the Sunrise/Melanin/Cold trinity. These are the original "technologies" that defend the IMJ against the heavy-neutron interference of deuterium from the unfettered electromagnetic spectrum in the Archean world which is now being built by the modern technological world.
Blockchain of Quantum Events: I've mentioned biology as a TIME blockchain. In this sense, the "consensus mechanism" of your health is the coherence of your Vagus Nerve. Every time you align with the natural light-dark cycle, you "mine" a coherent block and time controls the flow of energy in cells well.
Every time you rely on a "stolen" technological proxy (like a GLP-1 agonist), you allow a "fork" in your biological code that leads toward devolution via atavism. You lose time. Loss of time is an inflationary event for longevity. This is why GLP 1 drugs will shorten your life.
I am effectively arguing that we are living in a biophysical plagiarism. We have built a world that mimics our form but destroys our essence.
Elliot needs to brush up on the embryology of the face.
It is intimately linked to NCC which follow melanopsins lead into the cells that become the the mid face and jaws and they develop based on brain growth. I'm not surprised that a food guru has no clue how melanin from NCC drives this process. LOL.
Elliot seems to be ignorant that NCCs are the progenitors of both melanocytes and much of the craniofacial mesenchyme (e.g., maxilla, mandible via ectomesenchyme), tha tbecome the HUMAN FACE.
This shared origin explains evolutionary yoking of facial shape and pigmentation, as variations in NCC genes (e.g., Pax3/7) affect both melanin density and craniofacial morphology. Sorry to tell you Elliot, but it appears you are dumbass for not knowing how melanin is directly related to your double jaw surgery.
Low maternal UV/IR exposure is a known risk factor reducing melanin synthesis, increasing NCC vulnerability to apoptosis via chaotic UPE (ultra-weak photon emission), as NCCs are sensitive to oxidative stress in the embryo's face. Disruptions in NCC migration/differentiation lead to hypoplasia; e.g., in Waardenburg syndrome, and today it is well known by all except Elliot, that melanin defects correlates with craniofacial anomalies.
If the "mass" of NCC does not arrive to the correct sites in the embryo, the geometry of the face is never correct and leads to post natal deformities and associated risks.
The DC Current: In optimal health, the embryo generates a bioelectric field which forms primitive version of the Melanin-Water battery created by NNC and CCO function in mitochondria. This field acts as a "GPS" (Galvanotaxis) for NCCs to migrate into the somites and arches that form facial structures.
The Hypoplasia: If this current is weak (due to low maternal redox or nnEMF interference), the NCCs "stall" or "get lost in migration patterns of the embryo." This leads to Maxillary and Mandibular Hypoplasia (receded jaws), which can be the structural root of the Sleep Apnea. The "Mass" simply never arrives at the "Scene of face."
In the decentralized framework, Craniofacial Dysmorphology is a failure of Topological Embryogenesis due to altered DC electric currents that ultimate come from melanin via neural crest cells that have to migrate into the embryonic facial structures to complete its growth. The lack of neural crest cell (NCC) migration is the result of a "cold" or "dark" Bioelectric Field that fails to provide the DC current necessary to guide these cells to their destination.
The NCC "Galvanotaxis" Failure Neural crest cells are the "Exploratory Stem Cells" of the vertebrate body. They migrate from the neural tube to form the Maxilla and Mandible by following a voltage gradient.
The palate/jaw act as a mechanical resonator for brain growth, with receded mandible shrinking the airway, triggering Piezo1 sensors in the brainstem for a "bunker" response in sleep apnea. Bone's piezoelectricity generates DC currents during chewing to hydrate the "vascular pecten" via CCO that is needed to hydrate melanin for the DC current to be optimized in the picoampere range per Becker's work for bone growth.
The palate and jaw influence airway patency; mandibular hypoplasia in PRS or craniosynostosis causes glossoptosis and OSA via mechanical strain.
Piezo1, a mechanosensitive channel, is expressed in the brainstem and responds to stretch/shear stress, potentially linking airway obstruction to respiratory control disruptions in OSA. Bone is piezoelectric, generating DC currents under mechanical load (embryonic movement of tongue or chewing), which stimulates osteogenesis and vascular hydration of NCC derivative via CCO (cytochrome c oxidase) in mitochondria. Low NCC mass from defective maternal/paternal redox in their germlines reduce this "charge," impairing brain vascular support leading to aberrent craniofacial growth. Very embarrassing for you Elliot to be undressed a decade later wearing a T shirt that you never explored.
2. The interplay of NCC (melanin), the VDR and CCO on the IMM regulates mtDNA-driven melatonin production, which is critical for hormonal signaling and bone growth. Embryonic hypoxia disrupts CCO activity, CCO activity changes the DC current from melanin in NCC's and CCO is also capable of reducing melatonin and altering UPE transformation in embryogenesis, thus, damaging mtDNA via ROS, leading to altered developmental patterns in craniosynostosis (suture fusion), scoliosis(vertebral asymmetry), and malocclusions (maxillary/mandibular growth defects). Melanin and Melatonin links these conditions by modulating osteoblast activity and hormonal pathways (e.g., estrogen, IGF-1), while UPE and bioelectric currents (per Becker) provide biophysical signaling mechanisms that coordinate NCC and mesodermal development. VDR dysfunction amplifies these effects by impairing mitochondrial function and calcium signaling, particularly in NCC-derived tissues (maxilla, mandible, sutures) and mesodermal tissues (vertebrae).
Ultra-Weak Photon Emission (UPE):
UPEs, are generated by CCO activity and ROS in the IMM, and serve as a biophysical signaling mechanism, coordinating cellular differentiation and tissue morphogenesis. Reduced UPE due to impaired CCO (e.g., from hypoxia or VDR dysfunction) disrupt:
Suture patency, leading to craniosynostosis.
Vertebral symmetry, contributing to scoliosis.
NCC migration, causing maxillary/mandibular growth defects and malocclusions.
Melatonin, as an antioxidant created by ELF-UV light emission, reduces excessive ROS, helps create Vitamin D and stimulates the VDR on the IMM to affect electron tunneling, which can stabilize UPE signaling. Mitochondrial melatonin deficiency and altered DC currents from the hydration status of CCO on melanin will lead to erratic UPE patterns, disrupting developmental signaling in NCCs and mesodermal cells.....So Elliot you remain a dumbass for a decade now. I hope your oral surgeon is better informed so you do not get a nerve injury from this henious surgery. LOL
3. The "Mitochondriac" Conclusion: You cannot fix a "Proterozoic Face" with a dental appliance or a double jaw surgery, alone. You must restore the Picoampere Current by re-hydrating the Melanin via the Sunrise/Grounding/CT triad to reduce the risk of OSU in the adult. That is the evidence Elliot. You remain a clueless food guru.
Sleep apnea is the brain protecting itself from nnEMF and blue light. Oxygen is toxin to people with sleep apnea, and it also has a U shaped curve based on GOE evolution, hence why modern humans have it so commonly today since nnEMF mimics dehydration and hypoxia in our environment.
What did the blogs say about exogenous oxygen? Oxygen is quantized to the stoichiometry of the TCA/urea cycle. What if you Kreb's bicycle is dysfunctional because you never see the sunrise?
2. What happens to melanin when pseudohypoxia occurs due to nnEMF = Melanin dehydrates and become massively conductive in cells = Archean legacy = causes damage too all evolution built from the GOE onwards. No one sees it until they do.
3. Sleep apnea is the brain protecting itself from nnEMF and blue light. Oxygen is toxin to people with sleep apnea, and it also has a U shaped curve based on GOE evolution, hence why modern humans have it so commonly today since nnEMF mimics dehydration and hypoxia in our environment.
What happens to melanin when pseudohypoxia occurs due to nnEMF = Melanin dehydrates and become massively conductive in cells = Archean legacy = causes damage too all evolution built from the GOE onwards. No one sees it until they do.
Sleep Apnea is not a respiratory failure, but a Topological Defense Mechanism. The brain induces apnea to limit oxygen entry because, in a decoherent system, oxygen is the "match" that ignites the sPLA2-IIA Supernova to destroy organs.
If your nnEMF/Blue light environment mimics deuterium-induced dehydration, your Inner Mitochondrial Junctions (IMJs) collapse. You lose the CISS (Chiral Induced Spin Selectivity) needed to spin-match oxygen. In this "M1" state, incoming oxygen cannot be reduced cleanly to metabolic water. Instead, it creates a "flood" of Superoxide. The brain senses this oxidative "fire" and stops breathing (Apnea) to prevent the total destruction of the neural mitochondria. x.com/DrJackKruse/st…
My blogs and my thesis align on apnea being a "Proterozoic" survival strategy. Oxygen is a powerful paramagnetic radical. During the Great Oxidation Event (GOE), life had to evolve the Melanin-Metal shield and D-shell transition metals to "gate" oxygen.
Sleep Apnea is the body's attempt to regress to a Proterozoic state to survive a high-EMF environment. You aren't "missing air"; you are missing the Photonic DC current needed to make oxygen safe. This is a counterintuitive truth bomb of evolution on Earth through the GOE lens.
What did the blogs say about exogenous oxygen when melanin is not hydrated? Oxygen utilization must be quantized to the stoichiometry of the TCA/urea cycle. On the IMM sits CCO that makes the water that hydrates endogenous melanin. What happens if your Kreb's bicycle loops of TCA and urea cycles are dysfunctional?
This decentralized take implies solar light to stimulate melanin production on the skin is a better & safer option than using a apnea machine because most sleep MDs do not do matrix/cytosol stoichiometry testing on apnea patients to see how toxic oxygen is. This also explains why many people with apnea suffer from atrophic skin.
1. Question asked on the forum today: Hello all.
I'm $%^#@@ from Kansas City MO northern outskirts. 39° lattitude. 49 yo female
RLE surgery in left eye in December of 2023 (obviously before I found Dr. Kruse)...hopefully still getting enough beautiful sun in my one untouched eye.
Have faught with heartburn (small HH ) off and on for years...got off of H2 blocker 2 years ago and try to control mainly through diet/random supplements but phasing those out as I listen more to Doc.
Weak ass bladder after 2 kids that seems to get worse every year.
No other real medical history except some anemia the last few years (suspected d/t heavier periods/fibroids) and so my doctor currently has me on iron.
RN for 14 years now, bedside nursing, night shift...don't scold me...been making the transition to days since following Dr. Kruse and currently down to only one or two night shifts a month now.
Wearing my blueblockers most of the time, catching the sunrise and sunset pretty much most days since November and trying to get through Dr. Kruse's blogs the best I can without feeling too stupid. Plan on moving in the next few years after last kid is out of highschool. Where? I don't know...still have a lot of convincing to do to the spouse.
Hope to make it out to El Salvador for the 1st time this summer, maybe fall.
2. My ANSWER: This complex web of symptoms, ranging from eye surgery and heartburn to pelvic floor dysfunction and night shift challenges, reflects a deep systemic breakdown of the circadian and dopaminergic systems often seen in chronic metabolic conditions like diabetes.
1. The RPE-SCN "Optical Blindness"
The retinal pigment epithelium (RPE) and the suprachiasmatic nucleus (SCN), the body's master clock, are fundamentally linked through light perception and matrix metabolic regulation.
RPE Dysfunction: In night shift workers, high blood sugar causes early damage to the RPE barrier, leading to fluid leakage and "optical blindness" where the eye fails to properly process light-driven metabolic signals.
SCN Misalignment: When the RPE fails, the SCN loses its precise "zeitgeber" (time-giver) input. Working night shifts exacerbates this by forcing the body to operate against its natural light-dark cycle, leading to chronic circadian misalignment.
The "Untouched" Eye: Seeking sun in one eye while the other has undergone surgery (like RLE) may be an intuitive attempt to "re-sync" the SCN, though the systemic metabolic damage often persists across both eyes
3. The image highlights that UV-A and IR-A (Infrared) are the fuels for regeneration.
The Problem: In a modern environment (LEDs, screens, night shifts), we are often "UV-A/IR-A deficient" but "Blue Light toxic."
The Result: Without those specific frequencies, the RPE (Retinal Pigment Epithelium) cannot recycle the waste from your photoreceptors. This is the "optical blindness" where the eye is physically there, but the biochemical signaling of time is lost and this leads to all your current issues.
2. Dopamine, GERD, and Pelvic Floor Dysfunction
Dopamine acts as a bridge between your circadian clock and physical functions like digestion and muscle control.
The diagram shows Dopamine (DA) as the "Light" signal.
Muscle Fiber Type: low dopamine leads to muscle dysfunction. In my framework, dopamine is essential for maintaining the vagal tone and the correct "firing" of smooth muscles.
The GERD & Pelvic Link: If retinal dopamine is low, the signal to the brainstem is weak (PVN). This affects the Autonomic Nervous System, leading to the "loose" GE reflex (heartburn) and the "discordant" muscle tone in the pelvic floor. It’s not just a local muscle issue; it’s a top-down timing error you are experiencing from being a night shift nurse. My bet in your operated eye there was big time myopia of evidence of Drusen present.
Blue light and nnEMF toxicity often causes autonomic neuropathy, which delays gastric emptying and weakens the esophageal sphincter. Dopamine receptors (D2/D3) help regulate these digestive rhythms; when they are "out of sync," it manifests as chronic reflux or GERD.
Pelvic Floor Dysfunction: Chronic hyperglycemia damages the nerves and blood vessels supplying the pelvic floor. This can lead to diabetic bladder dysfunction (incontinence or urgency) and weakened structural support, which is further complicated by the "dopamine thing", as dopamine is essential for the coordinated muscle contractions required for pelvic health. The fact this is getting worse at 49 means your days of being a nurse should be over because you need a massive infusion of UV-NIR light during the day to fix all of this.
In your framework, mitochondrial haplogroups represent specific "evolutionary tunings" of the dielectric brake. The differences in Resting Metabolic Rate (RMR) and Total Energy Expenditure (TEE) are not just about ATP efficiency; they are about how different populations manage the Archean electrical surge from dehydrated melanin from CCO dysfunction relative to their ancestral light environment. This is why Wallace's maps helped me figure this out 20 years ago. Nick should asked me about the Archean epoch when we discussed GOE but we did not go there.
Originating in the high-UV environment of Africa, L haplogroups are highly coupled. In my decentralized thesis, "coupling" is the hallmark of a perfectly functioning dielectric brake.
The Thermodynamic Efficiency: Because they evolved under a consistent flux of NIR/Red light (380nm-NIR), their Cytochrome C Oxidase (CCO) is optimized to produce maximum metabolic water and this kept the electrical conductance of melanin low in our system.
Low RMR/TEE: This abundance of water keeps the melanin in the RPE highly hydrated (the "Golden State"). The melanin’s electrical conductivity remains low and "slow." Because the system is electrically "quiet" and efficient, the body doesn't need a high resting burn rate to manage thermal or electrical "noise." It is a state of maximum thermodynamic coherence.
BIOPHYSICS IS UPSTREAM BIOCHEMISTRY Nick. That was the story built in the Archean you never learned about, by design: Pergamon Press and McGraw Hill owned by those who control centralized science.
2. As humans moved to colder, lower-light latitudes, the NIR flux diminished. To survive, the "dielectric brake" had to be partially released to generate heat (thermogenesis) rather than just metabolic water.
The Uncoupling Strategy: These haplogroups are more uncoupled. In your framework, this means they intentionally produce less metabolic water per unit of fuel, allowing for a controlled increase in melanin’s electrical conductivity.
High RMR/TEE: The "unbridled" melanin generates more electrical friction/heat. A higher RMR is required to manage this "leakier" electronic state. These groups are essentially "closer" to the Archean state by design, using that "high-voltage" potential to maintain body temperature in the absence of strong solar flux.
3. This last tweet explains why uncoupled haplotypes need more fat and protein and less carbs. All about the dielectric brake no one learned about .........well I did because I asked follow up questions of my biochem professor, Peter Setlow.
So when you are uncoupled in high latitudes and around a shit ton of dehydrating polarized light you realize why blood glucose is skyrocketing and everyone has insulin resistance.
He says energy is repsonsible for all patterns of life forms. This was only true after the ozone layer was laid down in the GOE. This mindset has caused him to miss the most critical part of the story. Life organized outside to inside because of the Archean epoch before the GOE. This statement is at 2:04
When he goes on to say that UV light was important for developing mutations he is speaking centralized garbage. His mindset allowed him to completely miss the main purpose of UV light which was to develop allo-melanin and feodoxins before there was a shread of RNA on Earth. The basis of life began with abiotic dirty chemistry of the Archean which then developed because melanin provided protection without an ozone layer for the ferodoxin electron tunneling as the first heme protein. Melanin also provded away to clean the dirty chemistry by chelating metals and finding novel uses for them that would later become powerful to control the matrix. The most important thing he seems not to know melanin becoming hydrated by heme proteins is how the highly powered and chaotic light of the Archean was tamed to organize matter in a cell ---> set up the 0.66eV barrier to tunnel protons to build gradients for protocells, RNA/DNA/ATPAse etc....
He actually says the opposite of Wallace in his latest pod with Nick Jikomes. He says mutations are not welcomed when Wallce says they are. I am with Wallace and not Wunsch on this bigtime. 4:16.
He then makes the unbelievable statement that higher we go up on the evolution tree to us the more detrimental UV light becomes!!!! the oppsoite is true. UV light is the basis of photorepair for humans. This is ridiculous state and goes against the data in my pinned tweet and it goes against the why humans have so much melanin inside their body plans. Why leptin has a GOE level 220nm absorption spectra and why all LIVING CELLS emit ELF-UV. I could not believe Max did not say a word or push back hard on this. at 4:40-5:00
His point on Fraunhoffer lines is the first thing he says I agree with but he has zero idea how that linked to melanin in the Archean Earth and how it scales to humans today.
At 8:00 he talks about people living underground for long times and has no idea that this is what our ancestor mammals have done for 320 million years and the melanin on their surface is what allowed this to happen. He seems to have no Earthly idea that being underground puts you closer to uranium and thorium radiation which mammals can use to turn into useable energy. This guy is missing huge pieces of biology and I hate to say it, but I think if you listen to him about light you will become deeply misinformed. I like Wunsch a lot. Met him In Germany 7 yrs ago but instead of his thesis growing it has regressed toward centralization heat death.
This is my critique just ten minutes in. Honestly I would have never released this podcast because of the mistakes made early. Skipping this to get to the GOE and photosynthesis truly was a tragedy for decentralized truth.
2. At 22:00 he has completely disqualified himself as being a light epxert from my perspective when he says melanin pigment in the skin is not important. Just jaw dropping bad science.
3. Another huge gaff at 26:00. He says ATP is tied to warm and NIR light and totally diregards that UV-A light inhibits CCO to make ATP. Also Max not pushing back on this is shocking considering this is Wunsch's own slide on the topic.