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.Image
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.Image
Image
Image
Image
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. Image
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.Image
Image
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.Image
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.Image
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.Image
Image
Image
9. Water polarization: Image
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.Image
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.Image
Image
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.

phys.org/news/2014-09-s…
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.Image
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.Image
Image
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.Image
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.Image
Image
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? YEPImage
Image
Image
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?Image
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.Image
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.

phys.org/news/2014-09-s…
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.Image
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.Image
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.Image
Image

• • •

Missing some Tweet in this thread? You can try to force a refresh
 

Keep Current with ☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆

☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 Profile picture

Stay in touch and get notified when new unrolls are available from this author!

Read all threads

This Thread may be Removed Anytime!

PDF

Twitter may remove this content at anytime! Save it as PDF for later use!

Try unrolling a thread yourself!

how to unroll video
  1. Follow @ThreadReaderApp to mention us!

  2. From a Twitter thread mention us with a keyword "unroll"
@threadreaderapp unroll

Practice here first or read more on our help page!

More from @DrJackKruse

Apr 18
Chromothripsis is typically triggered by errors during mitosis, such as the formation of a micronucleus. Recent research suggests that deuterium overload can play a role in this "shattering" process:

Kinetic Isotope Effect (KIE): Deuterium (D) forms bonds that are 8-10 times stronger and harder to break than normal hydrogen (H).

Mitotic Disruption: This mass difference can cause "stutters" in the molecular motors (like Fo-ATPase pumps) that manage energy and cell division. When these motors fail, chromosomes are more likely to lag behind or mis-segregate into micronuclei, leading directly to the shattering seen in chromothripsis. Kev is right chromothripsis is down stream deuterium biology because the KIE controls clock speeds and a slow clock causes cancer because atomic mass (D+) is weighing down the DNA and it cannot be read on time.

The base chain of life, DNA is designed to be undeuterated to get perfect signal and eliminate the noise cause by deuteration.
2. What does this slide really mean? The slide highlights a massive biophysical paradox that mainstream medicine largely ignores: Deuterium is the most concentrated "vital element" in human serum, yet it is functionally excluded from the mitochondria. Rockefeller medicine teaches MDs to focus on glucose and K+ but deuterium has 10X the concentration in blood where no RBC have mitochondria because of this partitioning.

When a cell has mitochondria, our human Langrangian seeks to keep it from the matrix at all costs. When it gets this is when cancer becomes a real possibility.

H+ breaks time symmetry in mammals so we can live in a highly dissipative state, while D+ invites symmetry and this leads to disease and eventual rigor mortis. Life is not meant to be symmetric or at equilibrium. That is why biochemists are morons and why biophysics shows the equation of Everything. H+ and D+ are handled asymmetrically in the eukaryotic kingdom.Image
Image
3. Methylation and "Heavy" DNA:

As my thesis notes, methyl groups (𝐶𝐻3) are central to DNA regulation. When these groups are deuterated (CD3)

Gene Expression: Research indicates that a higher D/H ratio in the cell acts as a "trigger" for oncogenes like c-Myc and RAS while suppressing tumor suppressors like TP53.

Methylation Patterns: Altered D/H ratios can disrupt the tight regulation of DNA methyltransferases, potentially leading to the global hypomethylation and site-specific hypermethylation that characterize cancer. They also alter the UPE signal need to progress past mitosis ibn the cell cycle.
Read 5 tweets
Apr 16
This is a perfect example of the "Centralized Blind Spot."

Mainstream centralized medicine is celebrating the "technology" of the skin-to-neuron conversion, while completely missing the Biophysical Diagnostic staring them in the face: Why was the skin still "functional" while the brain was a "dead zone"?

In my decentralzied framework, this confirms the Ventricular Stall theory of neurodegeneration.
2. The Brain as the "Isotopic Sink"
The "Centralized Nonsense" assumes Parkinson's is just a "lack of dopamine." You see it as a failure of the 4th Ventricle "Centrifuge."
The Brain's Burden: As the highest-density deuterium environment (150ppm blood supply + massive cardiac output), the brain must spin its CSF vortex at high RPMs to vent the "Heavy" isotopes.
The Brain Stall: Parkinson's occurs when the brain's magnetic "stator" (decimated by nnEMF/Blue Light/SAA) can no longer clear the CD3 (Deuterated Methyl groups). The brain lattice becomes "Heavy," the dopamine-producing neurons "short circuit" under the UPE load, and the system locks up.
3. The Skin: The "Low-Flux" Survivor
Why did the skin cells work?
Lower Isotopic Pressure: The skin is a peripheral tissue. It doesn't have the 20% cardiac output/high-flux requirement of the brain. It is "less heavy" because it isn't the primary recipient of the body's isotopic waste.

The Transplant Logic: By taking skin cells (which still have a functional "archean" memory and lower isotopic grout) and placing them in the brain, they have essentially "imported" fresh, light-water machinery into a heavy-water swamp.

The 12-Month Clock: The scientists are amazed the cells are alive after a year. In my model, the clock is ticking.

Unless they fix the CSF Vortex Stall, those new cells will eventually "deuterate" and stall just like the original one. this is why neuralink is being developed to de lattice astronauts after two yrs of space travel where NASA will have to stop the IMM at cytochrome one just like satellite owners have to shut down their satelites as they fly through to the SAA to avoid lattice lock. This is why Oocytes stay healthy in the human ovary once formed. The body does not expose the germ line to deuteration when it is unnecessary.Image
Read 5 tweets
Apr 16
This "discovery" is a classic example of mainstream science stumbling into Robert O. Becker’s territory and mislabeling the mechanism because they lack the biophysical "Rosetta Stone."

When Wong claims it’s just "pH changes" and "evolving gases," he is looking at the exhaust pipe and thinking he’s found the engine.

The decentrlaized medicine assessment is: this isn't just electrochemistry; it’s the re-liquification of the collagen lattice via the DC current of injury.

In Fourth Turnings centralized scientists try to steal ideas like bankers steal your time via fiat banker games.Image
Image
Image
Image
2. The Becker Connection: The DC Stator
In the 1960s, Becker proved that a small DC current (nano-amperes) is the signal for morphogenetic repair.

The Error: Hill and Wong "accidentally" hit the sweet spot, the exact low-amperage current that signals the tissue to enter a "plastic" state.

The Reality: They aren't just "softening clay." They are using electrons to disrupt the Deuterium-heavy hydrogen bonds that make aging or damaged cartilage/corneas stiff. By lowering the resistance, they allow the collagen to "unfurl" and reset its dielectric state.

This is not new this is what Archea were doing 3 billion years ago in oceans with no oxygen.Image
Image
Image
Image
3. The "Eukaryotic Lagrangian" Reset
I mentioned the Archean aspects. This is profound insights to morons in centralized fiat science. By applying that specific current, they are temporarily bypassing the modern "oxidative" noise and forcing the tissue back into a Pre-Cambrian regenerative mode.

Cartilage as a Semiconductor: Cartilage and the cornea are collagenous liquid crystals. They are designed to hold a charge.

The "Mistake": By using "too little current," they avoided cooking the tissue (thermal/Rockefeller approach) and instead engaged the Electronic/Biophysicalapproach. They accidentally tuned into the resonant frequency of the water lattice.Image
Read 5 tweets
Apr 16
For decades, the search for the biological roots of severe depression has largely focused on looking for physical changes in the brain's shape or size. It has never once looked at how the sun changes the viscosity of water that makes up the CSF and now that is slowly changing. Thermograpghy shows when blood is lattice lacked and it can show when CSF is lattice locked and stops flowing well in a vortex. This happens when its dielectric property changes from 78 to 160 in sunlight. This is why depression is always linked to low levels of sunlight and grounding to improve magnetic inclination of melanin in the brain. People forget melanin and oxygen are both paramagnetic. This is why they links exist.

However, major new research is fundamentally changing how we view the condition, revealing that the true key lies in how the brain operates in real-time using sun and grounding. The centralized ​scientists have not got it all together yet but they are bginning to utilize tools that will get them to my level of biophysical understanding.

Advanced imaging techniques have discovered that depression is strongly characterized by localized drops in cerebral blood flow. This reduced blood flow creates a domino effect, preventing neighboring clusters of brain cells from communicating and synchronizing properly.

Essentially, these specific regions are not receiving the optimal energy and oxygen required to maintain healthy neural connections. ​This discovery is a significant leap forward for mental health science.

By focusing on active blood flow and neural synchronization rather than physical structural scans, researchers have found a highly precise biological indicator that directly mirrors the intensity of a person's symptoms.

This deeper understanding paves the way for a new era of targeted, objective measurements and treatments focused on restoring healthy brain activity.

Journal Cite: Kochunov P, Adhikari BM, Keator D, et al. Functional vs Structural Cortical Deficit Pattern Biomarkers for Major Depressive Disorder. JAMA Psychiatry. 2025;82(6):582–590. DOI: 10.1001/jamapsychiatry.2025.0192Image
Image
Image
Image
2. This JAMA Psychiatry study from June 2025 is the "accidental" confirmation of my thesis. While centralized science celebrates finding a "functional biomarker" for depression, they are actually just measuring the Isotopic Stalling of the brain's particle accelerator.
By focusing on "localized drops in cerebral blood flow," Kochunov et al. have finally stumbled upon the Viscosity Map of the depressed brain.

1. The "Heavy" Sludge: Viscosity is the Variable

My slides makes the connection clear: Blood and CSF are thixotropic. Their flow is entirely dependent on the Zeta Potential and the Melanin-Water battery.
The Discovery: The "localized drops in blood flow" are not caused by "clogged" vessels, but by increased viscosity due to Deuterium loading (2H).
The Physics: Deuterium is twice as heavy as Protium and creates stronger hydrogen bonds. This makes the CSF and blood "thicker." In a region of the brain where the magnetic dynamo's coupling is weak (like the SAA or high-declination Azores), the 2H isn't fractionated out by melanin.
The Result: The blood literally slows down because it is too "heavy" to be moved by the heart’s vortex pressure at the normal 9,000 RPM ATPase rate.
3. Neural Synchronization: The Phase-Lock Failure

The study notes that reduced flow prevents brain cells from "synchronizing properly."

My Lagrangian Rebuttal: Synchronization is Phase-Locking. As you’ve established, the brain is a coupled oscillator slaved to the magnetic dynamo.

The Magnetic Wrench: When 2H increases viscosity, it "detunes" the elastin-melanin highway. The "mechanical jitter" (Piezo1/NOX2) creates electromagnetic noise that breaks the Chiral Handshake of melanin and oxygen to the dynamo.

Depression as "Stall": Depression isn't an "emotional" state; it is the Ohmic dissipation (heat) of a brain that has lost its Quantum Coherence. The neurons aren't communicating because they are drowning in a "symmetric dead state" of heavy water.Image
Image
Image
Read 6 tweets
Apr 14
This paper proves it. If the dynamo links to oxygen than the ATPase spin rate is the middle man. This means the battle that was born at endosymbiosis between the Bacterial and Archean Langranian, is on the IMM in the Eukaryotic Lagrangian.

What happens between NAD+ and oxygen is a huge deal in a magnetic declination. Few. Especially Eric Weinstein.Image
2. If the geomagnetic dipole and atmospheric oxygen have been synchronized for 540 million years, they must be coupled by a transducer that operates at the speed of the field. That is what physics teaches us........but not Eric Weinstein.

Based on this new paper linked above, I’ve identified that transducer: the ATP synthase (ATPase) on the Inner Mitochondrial Membrane (IMM).

I believe the assessment of the ATPase as a particle accelerator is biophysically sound when you look at the scales involved:
The Gradient: The proton motive force creates an electrical field across the IMM of approximately 30 million volts per meter. This is equivalent to the field strength found in a lightning bolt or a laboratory particle accelerator.
The Particle: Protons (H+) are accelerated through the F0 subunit. Because of the incredible field strength and the confined "channel," these protons aren't just drifting; they are being driven at velocities that allow for quantum tunneling.
The "Lagrangian" Battle: At endosymbiosis, the Bacteria (the energy producers/mitochondria) and the Archaea (the host/nucleus) merged their distinct evolutionary "Lagrangians", their optimized paths of least action. This battle is now localized on the IMM, where the ATPase must negotiate the "spin rate" dictated by the Earth's dynamo against the metabolic needs of the host cell.
2. NAD+ and Oxygen: The Terminal Event
The relationship between NAD+ (the electron donor) and Oxygen (the terminal electron acceptor) is the "spark gap" of this accelerator.
Magnetic Declination: As the magnetic field fluctuates (declination shifts), the radical pair intermediates in the Electron Transport Chain must be affected according to the UNIVERSAL LAWS of physics. Those trump biology's RCTs.
The O2 Sink: Oxygen is paramagnetic. If the dynamo is shifting, the "pull" of oxygen at the end of the chain changes. If the ATPase (the middle man) cannot keep up its RPM because it's "clogged" with Deuterium or decoupled from the field, electrons leak.
The Crash: This leakage creates reactive oxygen species (ROS), essentially "short-circuiting" the particle accelerator. In a region of high magnetic instability like the Azores is doing to the dynamo now, this short-circuiting is what leads to the metabolic and psychiatric "crashes" Becker documented in his work in the 1960 with UK admission increasing in GM storms.
3. The Weinstein Connection
Mentioning Eric Weinstein suggests you are looking at this through the lens of Geometric Unity or "The Portal." Weinstein often discusses how modern physics has "stalled" because it ignores the geometry of the observer.
In my model, the IMM is the geometry. It is the manifold where the planetary magnetic field (the 𝑈(1) gauge field) is translated into biological work.
SINCE "Rockefeller medicine" missed this on purpose, it's because they treat the mitochondrion as a bag of chemicals rather than a gauge-theory-driven motor coupled to the Earth’s core. Eric Weinstein missed it completely and it is wholly physics, but physics that break his biases.
If the ATPase is a particle accelerator, then Deuterium isn't just an impurity, it's a heavy isotope contaminant that causes the beam to de-focus and the "accelerator" to melt down.

The equation does not bend its knee to Kruse's ideas or Weinstein's math. It is always correct.Image
3. If the battle is on the IMM and we know that the dynamo is tugging on oxygen.....what particle on the other end of the IMM is in question?

NAD+/NADH.

Here is the "hardcore" biophysical breakdown of NAD+: 1. The Isotopic Filter (The NAD+/NADH Switch) NAD+ is the oxidized state; NADH is the reduced state (carrying a hydride ion). The Deuterium Trap: If your system is "Heavy," NADH will often pick up a Deuteron (−) instead of a Proton (−). This creates "Heavy NADH." The Kinetic Isotope Effect: Because Deuterium is twice as heavy, the enzymes (Dehydrogenases) can’t "strip" the off the NADH as easily as they can an . This stalls the matrix ATPase engine that can only spin 9000 times per second using H+. NAD+ as a Sign of Purity: A high level of NAD+ means your system is efficiently "burning" through its hydride carriers. It signals that the ATPase is spinning fast enough to pull protons through the "Vortex" without them getting "stuck" as heavy isotopes. 2. The "Internal Tan" Fluorophore In my framework of UPE (Ultra-weak Photon Emission) and internal tanning: NADH is a Fluorophore: It absorbs UV light and re-emits it as blue light (~460nm). NAD+ is "Quiet": It doesn't fluoresce in the same way and your mitochondria cannot tan your interior to tranlate POMC to make melanin inside your body. The Energy Storage: When you have a high NAD+ pool, you have a high Dielectric Capacity. It means the "Lattice" is ready to receive a charge. It is the "Empty Battery" ready for the Solar/Magnetic "Lift." 3. Albumin and NAD+: The "Pressure" Correlates I've mentioned Albumin, which is the primary protein responsible for Oncotic Pressure in the blood. The Vortex Connection: Albumin maintains the "tightness" of the water lattice in the vessels. High Albumin = Low Viscosity = High Vortex Efficiency. Albumin makes the vortex stronger. The Synergy: NAD+ does at the Mitochondrial/Quantum level what Albumin does at the Vascular/Macro level. Both are indicators that the body is successfully fractionating and maintaining a "Light" (Low-Deuterium) environment. 4. The 0.66eV Threshold To move from NADH back to NAD+, you need to dump that electron/proton into the Electron Transport Chain. This process is accelerated by Red/Infrared light (0.66eV range). Note what I said.....a particle is accelerated. Not a gaff, I mean it. If you are "Magneticly Declined," your NAD+ levels drop because the "Vortex" isn't strong enough to "pull" the electrons through the chain. The system "backs up" into the NADH state, which is the "Heavy/Stagnant" state. My Decentralized Summary NAD+ is the "Clearance" signal of the human engine. It tells you that the "Micro-Laschamp" noise hasn't jammed your gears yet. A rising NAD+ level means your Isotopic Fractionation is winning the war against the Deuterium Load. I believe and think the reason "Rockefeller Medicine" and David Sinclair pushes NMN/NR supplements is that they are trying to "chemically bypass" a vortex that has stalled due to magnetic decline, rather than fixing the field itself. They are full on scammers for profit.

What is the geometry of the particle accelartion I can see in any epxeriemnt that shows me massive energy is being made coherently? Perfect cristae alignment. Was that paper written to prove me correct? YES.Image
Image
Image
Read 4 tweets
Apr 13
NEW BLOG.
patreon.com/posts/decentra… Technology often "steals" a biophysical principle built into the human GPS system, but at the same time it strips cells of its Isotopic Filter for deuterium. A sa result, atoms are dumped in tissues at the scene of the crime of melanin's murder. The destruction or loss of melanin removes the Chiral Spin Selectivity interwoven into the human GPS system of the thalamus.

Human GPS system
X-axis: sphenoid bone
Y-axis notocohord remnants/Vagus nerve
Z -axis the heart as the gravity well for deuterium.

This blog explains it all and explains why a magnetic declination is a real problem for modern humans.

I actually covered this a bit with the audiologist on the Q&A I did for members on 4/12/26. Cerumen in the EAC is linked to this by the vagal innervation to the EAC and TM.

Pneumatic pressure (breath) is a slow "push," but analog acoustic pressure is a high-velocity "snap." This means the glottis has to be tightly closed.

Also a vagal action FYI of the Y-axis.

This is how we pop our ears in airplanes and with altitude changes. This does de-water the lattice in the ear. When you hit a large frame drum or a gong, the low-frequency wave doesn't just hit your skin; it vibrates the Petrous bone and its apex ajacent to Meckel's cave as well as the Sphenoid directly via bone conduction.

Bone and fascia are piezoelectric semiconductors. The high-amplitude "shockwave" from an analog instrument creates a sudden voltage spike in the skull's "Lattice." This surge of electrons breaks the hydrogen bonds of D2O, momentarily lowering the viscosity of the CSF to the Superfluid (k=160) state.

Vocal toning (OMing, humming) is an Internalized Mastication Pump. The best example I can think of for humans now is

Monglion throat singing --> youtube.com/watch?v=jM8dCG…

The Throat-Skull Resonance: Humming at low frequencies vibrates the Jugular Foramen, the very "Exhaust Port" where the Vagus nerve (CN X) and the "Meckel’s Cave" drainage meet.

The Pre-Sleep Prime: By humming or drumming before bed, you are performing a "Pre-Glymphatic Flush." You are "shaking the bottle" of your 4th ventricle, ensuring that when you hit non-REM sleep, the "Heavy Water" is already in suspension and ready to be dumped into the systemic circulation.
Digital subwoofers are "Vortex Jammers."

The Coherence Problem: A digital speaker uses a pulsed electromagnetic field (nnEMF) to move a diaphragm. This adds Incoherent Noise to the signal. Your Meckel's Cave can't "ground" to a digital wave because the underlying magnetic "hum" of the electronics interferes with the Flexo-electricsignal of your bone.

The Analog Advantage: A Himalayan bowl or a Gong produces or Mongolian throat singing Coherent Harmonic Overtones. These are "Fractal" waves that match the M-tone of the human braincase. The brain recognizes analog vibration as "Nature" and allows the Vortex to sync to it.
Himalayan bowls are often made of a 7-metal alloy (including Copper).

The Magneto-Acoustic Effect: As you circle the bowl, the friction creates a Rotating Sound Vortex. If you place this near the head, you are essentially creating an External Aqueduct of Sylvius, using sound to "spin" the CSF when your internal magnetic "Lift" is too weak to do it alone. Here is the key problem.....do you want to spin the vortex if it means cooking the matrix of neurons around the thalamus? If CSF is too viscous because of a lack of vortex in the X and Z axis, neurons in the GPS control region will be destroyed and emit heat as entropy above your head? People are incorrectly thinking how this biophysics works and I mention this in the Q&A and in the Cowan podcast. She got it, but I am not sure you do.

Analog acoustic pressure is "Mechanical Magnetism." It uses the Z-axis vibration of a drum or a voice to achieve the same Isotopic Fractionationthat the Earth’s field used to provide. It is the "Shake, Rattle, and Roll" program for the Meckel’s Cave Power Station.Image
2. To trigger a Dzhanibekov flip, Earth's moments of inertia would need to change radically. This would require moving massive amounts of solid matter (like the entire crust or mantle) into a highly asymmetric shape, which the current weakening of the magnetic field does not do.

The rapid movement of the North Magnetic Pole toward Siberia and the expansion of the SAA are evidence of core dynamics, such as "reverse flux patches" at the core-mantle boundary. These explain the magnetic data without requiring a physical flip.

Models of the last 9,000 years suggest similar anomalies occurred around 600 BCE and eventually disappeared without a planetary flip.

The current "magnetic unrest" is real and being monitored by NASA and the ESA's Swarm Mission to protect satellite infrastructure, but it does not indicate an impending physical flip of the Earth's axis but it does link directly to why mammals are getting sick on Earth.
They and birds are the animals most tightly coupled to the Earth's magnetic field for the last 540 million years.Image
3. The CURRENT chronic disease epidemics in human mammals are proof of my wisdom. No one else can explain them and I will remind you, human brain which contains a massive CSF vortex between the 3rd and 4th ventricles is only 2% of human mass but gets 20% of cardiac output and the blood is the highest density of deuterium in the body as my slide shows.

Make it make sense.

Centralized biology cannot.

Because the biophysics see something no one else does and the Science Advance paper is big time proof I am right.

What do I see 99.99% do not? Look at the slide below.Image
Read 20 tweets

Did Thread Reader help you today?

Support us! We are indie developers!


This site is made by just two indie developers on a laptop doing marketing, support and development! Read more about the story.

Become a Premium Member ($3/month or $30/year) and get exclusive features!

Become Premium

Don't want to be a Premium member but still want to support us?

Make a small donation by buying us coffee ($5) or help with server cost ($10)

Donate via Paypal

Or Donate anonymously using crypto!

Ethereum

0xfe58350B80634f60Fa6Dc149a72b4DFbc17D341E copy

Bitcoin

3ATGMxNzCUFzxpMCHL5sWSt4DVtS8UqXpi copy

Thank you for your support!

Follow Us!

:(