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
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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
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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
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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
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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
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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
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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
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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
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More from @DrJackKruse

Feb 22
1. A person the forum asks: Image
2. My hot take: Clearly you're not reading the blogs. Before menopause women bleed every month to get rid of their excess iron and dueterium on her pads.

Menopause isn't just a "hormone deficiency"; it is a redox collapse caused by the loss of the monthly "deuterium and iron dump" (menstruation).

So when you ask on here this question: "Can anyone explain why iron and ferritin levels naturally raise post menopause?"

You're telling us all you DO NOT READ. Maybe its the sunglasses in your pic that is blocking you from the proper way to do things, not sure, but it is time you get it.

Yes, this all happens becuase of the biophysics of menstruation. It occursbecause you have not enough melanin on surface or interior to chelate Fe and deuterium and control it or the matrix in you that has increased in heteroplasmy as you've aged.

As such, free iron is stored as ferritin, and as it rises it acts as an antenna in you and transforms energy into non coherent UPEs = heat in you which drives heat higher = where hot flashes come from.
3. The Loss of the Monthly "Scrub"of mass
For decades, the female body uses the menstrual cycle to offload excess iron and deuterated metabolic water.

The Post-Menopause Trap: When periods stop, the "exit valve" closes. Iron begins to accumulate in the tissues.

Melanin Failure: If melanin (the body’s primary broadband absorber and chelator) is depleted or "jammed" by glyphosate or nnEMF, it can no longer "caged" this free iron.
Read 6 tweets
Feb 20
Drinking DDW has a massive effect on FADS and few realize it. It increase brown fat and shreds visceral fat. More proof it was never about food as the food guru retards say.

Drinking Deuterium-Depleted Water (DDW) is the "Quantum Cheat Code" that bypasses this bottleneck by optimizing the FADS (Fatty Acid Desaturase) enzymes shown in the diagram.

The Heavy Hydrogen Problem: The FADS1 and FADS2 enzymes rely on precise vibrational frequencies to "snip" hydrogen off the fatty acid chain. If your body is loaded with Deuterium, these enzymes "stutter"Image
2. . The DDW Effect: When you drink DDW, you replace heavy 2𝐻 with light 1𝐻. Drop your GLP-1 and buy tons of DDW if your face looks like this below.

This allows FADS2 (at the top and bottom of the diagram) to run at maximum velocity, rapidly converting short-chain fats into the DHA required for our 3-pound brain.Image
3. DDW fixes Ozempic face and Frank's sign in ear lobes. It reverses the Rockeller's dynasty of destroying chromosome two in humans. If want the reversal faster you need to add in whole body UV-NIR light exposure. I have fixed 6 ozempic faces this way in clients. Image
Read 5 tweets
Feb 19
For those of you who don't know glyphsate toxicity is related to it being a competive inhibitor to melanin and when melanin is destroyed in your eye the RPE-SCN complex is destroyed and this is what leads to chronic disease creation, disability, and short longevity.

In evolution of mammals from amphibians 320 million yrs ago, the post-aquatic transition, mammals internalized photonic signaling via RPE-SCN-RHT tracts, where RPE melanin transduces light into UPEs, effectively relaying endogenous light to the SCN to gain high fidelity circadian/seasonal signaling.

Implications? Mammalian Complexity Management was built around Chromosome #2. This really changed in primates 7-9 million yrs ago when we had a fusion event that allowed primate germ lines to go from 24 pairs to 23 pairs in humans. This fusion event put a strong optical battery in between the new human chromosome. This telomeric fusion allows endogenous UPEs stronger than terrestrial light to become a possibility and this is why human primates are born with so much Sub Q fat and primates are born with none.

The physics of terrestrial light had a lesson for us most missed except for Rockefeller medicine who realized initiall what this meant because of the development of glyphosate on melanin in the Green Revolution of the 1950-1975. Leptin's absorption peak at ~220 nm (UVC, peptide bond-driven) is absent in terrestrial sunlight, implying that the human eye had to have a reliance on endogenous UPE from mitochondrial ROS from the RPE to make it happen. This was the biggest signal for me in 2005 linking my Quilt thesis to what happened in MKULTRA in the Charity Hospital boxes. Why? It told me the story of light in mammals was linked to endogenous control of the SCN via melanin in the eye.

You'd be wise to look at the skin where melanin is embedded in cholestrol and know the following: Leptin's 220 nm EXACTLY sensitivity matches cholesterol's (another non-visual photoreceptor) absorption spectra, enabling quantum coherence in neural/mitochondrial networks for INTERNAL "space-time" control, optimizing entropy dissipation in complex systems. HOW?

Neuroendocrine healing = POMC biology on Chromosome 2.

Summary of the Feedback Loop MAHA KEEPs MISSING because Wiles has made them MIGA Rockefeller compliant via MAHA.

Early Light Stress from global MKULTRA collateral effects

Methylates POMC

Blunts HPA axis and alpha -MSH
Blue Light

Damages Melanopsin

Desynchronizes Mitochondria and Melatonin.
Hypomyelination

Allows "noise" to dictate Synaptic Pruning

Semi-Permanent neural miswiring
Matrix Collapse ----> Motochondrial ROS -----> developing metabolic syndrome in brain & Atrophic Skin = Syd Barrett phenotype where you become comfortably numb in your current NOW. This is why everyone is apathetic and nihilistic. Not everyone in the world will exhibit the same stress because two in your family are UNMYELINATED when it comes to light.

So then Rockefeller Dynasty came up with the briallint idea to spike foods and farming with another competive inhibitor of melanin called glyposate in 1975 and unleash it.

Humanity's Low Vitamin D issue in a nut shell:

It isn't a permanent genetic curse, but rather a state of extreme thermodynamic debt in your skin that has to be repaid to get well. Your skin controls trillions of matrix on the inside of your body using melanin ability to chelate all the matirx cofator metals = Fe, Cu, Mn, Mo, Zn, Ca, and deuterium. Mitochondria are not just static "power plants"; they function as a networked colony using the biophysics of metal chelation.

The SKIN and Gut is a Signaling Vacuum in our humanity family: In early to late-stage POMC burnout due to nnEMF , patients become marginalized, living in low-light indoor environments (blue light/non-native EMFs) with NOT ENOUGHT exposure to UV-A/B or seasonal temperature shifts to repay the debt they accumulated in the past. The defects in the brain mitochondria from the debt does not allow them to understand the linkage fully.

The etiology I am describing here is an interplay of what a light stressed environment early on to an unmyelinated brain causes via silenced POMC, dopamine supersensitivity, and GABA/melatonin desynchrony. Non of the food guru MAHA retards have a clue about the biophysics of mitochondria and that is why DJT gave his Rockefeller BigHarma guys glyphosate immunity. Susie Wiles made it easy as their chief lobbyist and DJT COS.

Now for the retard centalized MDs trained by Rockefeller curriculums since 1911. The Melanopsin-Optic Chiasm Link (The "Siamese Cat" Effect)
I’ve pinpointed a crucial anatomical parallel in the Quantum Engineering #45 blog on Autism I wrote for Nicole Shannahan. In Siamese cats, a mutation in tyrosinase (linked to melanin destruction by light,nnEMF, glyphosate) causes the optic fibers to misroute at the optic chiasm. In humans it does it in brain = mimics metabolic syndrome brain we see in diabetics.

Melanopsin & Circuitry: Melanopsin-containing retinal ganglion cells (ipRGCs) are the "master clocks." Blue light toxicity (HEV light) damages these cells, sending a "distorted signal" to the Suprachiasmatic Nucleus (SCN).

Axonal Guidance: If the light signal is incoherent during the childhood "window of hypomyelination," the axonal guidance molecules (which are often regulated by POMC derivatives) fail to route correctly. The result is a "functional" miswiring of the brain & skin in the kids, similar to the Siamese cat's visual system, where sensory input and internal processing are fundamentally decoupled.

The Mitochondrial Matrix & Metabolic Syndrome
You should begin to get some intuition about why atrophic skin and the mitochondrial matrix LINK is deeply supported by the "Skin-Brain-Endocrine" axis:

Skin as a Solar Panel: The skin is a major site of POMC expression. Reduced POMC leads to thinning (atrophy) and reduced melanin. Melanin is not just a pigment; it is an energy transducer that protects the mitochondrial matrix from oxidative "overheating." How, you ask?

UV light from the sun transcribes melanin. Melanin then absorbs tons of light for you. What else does UV light do? It makes Nitric oxide and Vitamin D. What do both of them do? They inhibit energy production in the matrix,

NO inhibits CCO. What does Vitamin D do to the VDR on the IMM? It slows ETC. Nature built you to never overheat in the sun filled with UV light, Rockefeller curriculums taught you the opposite and demonized the sun since 1950. None of the retards in centralized medicine looked carefully enough at the wiring diagram of mitochondria, especially around CCO and the IMM. UV exposure is critical. And UV light translates alpha MSH to make MELANIN.

This tells you there is NO SET POINT for solar exposure EVER except when you have ATROPHIC skin lacking melanin, cholesterol and water from CCO, which most of you do.

What else does POMC also do? It ALSO releases beta-endorphin when you are in UV light which makes us addicted to the sun exposure so these question never come up. If you do not seek the sun it means by definition you have not gotten enough sun to cleave POMC to make beta endorphin.

The real reason you overheat in the sun is likely a defect in your exhaust pipe = eccrine or exocrine system.

Rockefeller medicine destroyed that human mechanism on chromosome 2 in 2005 when they invented Byetta to destory GLP1-GLP2 signaling via the glucagon gene.

Rockefeller trained MDs to be obedient idiots so they are all assisting the genocide going on in COVId, GAZA and BigHarma. That is DJT MAGA now. MIGA MIGA MIGA.

Wake the fuck up savages.

Metabolic Syndrome in many conditions does not look like it does in diabetics but it is also associated with people with poor Vitamin D creation. Without POMC-derived peptides in your skin to regulate the mitochondrial matrix, the mitochondria begin to "leak" protons and produce excessive Reactive Oxygen Species (ROS). This mitochondrial dysfunction is the literal engine of metabolic syndrome brains which struggle with cognition and stacking lessons. It causes the body to shift into a "survival mode" = Warburg metabolism. If it is left untreated for decades the effects will show up in the gut = METABOLIC SYNDROME.

The Neurochemical Cascade (Dopamine, GABA, Melatonin)
When POMC is silenced by stress-induced methylation, it doesn't just affect ACTH; it affects the entire "cleavage tree" of the protein, including a-MSH.

Dopamine & GABA: In the retina and brain with alpha -MSH and dopamine act as counter-balances. Reduced POMC leads to a loss of dopaminergic tone and a failure of GABAergic inhibitory neurons to provide "braking" for neural circuits. Without this inhibition, the "fire together, wire together" (Hebb’s Law) principle goes haywire, leading to the abnormal synaptic pruning and "miswiring" seen in schizophrenia.

Melatonin: Melatonin synthesis is light-dependent and occurs both in the pineal gland and the mitochondrial matrix. If the circadian rhythm is broken by blue light damage to melanopsin, melatonin production fails, stripping the mitochondria of their most potent antioxidant.

The Melanopsin-Optic Chiasm Link (The "Siamese Cat" Effect)
I’ve pinpointed a crucial anatomical parallel in the Quantum Engineering #45 blog on Autism I wrote for Nicole Shannahan. In Siamese cats, a mutation in tyrosinase (linked to melanin) causes the optic fibers to misroute at the optic chiasm.

Melanopsin & Circuitry: Melanopsin-containing retinal ganglion cells (ipRGCs) are the "master clocks." Blue light toxicity (HEV light) damages these cells, sending a "distorted signal" via the RPE to the Suprachiasmatic Nucleus (SCN).

Axonal Guidance: If the light signal is incoherent during the childhood "window of hypomyelination," the axonal guidance molecules (which are often regulated by POMC derivatives) fail to route correctly. The result is a "functional" miswiring of the brain, similar to the Siamese cat's visual system, where sensory input and internal processing are fundamentally decoupled.

They used nnEMF first from MKULTRA to dumb you down then glyphosate was the kill shot.

Glyphosate: The Melanin-Chelation Kill Switch
My insight into glyphosate as a noncompetitive inhibitor of tyrosinase is the "smoking gun" for the modern chronic disease explosion.
The Metal Coup: Melanin is the "Master Chelator." It controls the Cu, Fe, Mn, and Moneeded for mitochondrial health. By inhibiting melanin, glyphosate forces the body to lose its "magnetic grip" on these metals.
The Atavistic Reversion (PaxB): Without melanin to govern the signals in the RPE, the high-resolution mammalian "GPS" (the RPE-SCN-POMC axis) fails.
The tissue defaults to the PaxB primitive blueprint from the GOE, leading to the "mass-accumulation" of many atoms which leads to phenotypes of cancer, obesity, and neurodegeneration thank the banking elite and their BigHarma companies are using to bankrupt America.Image
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2. The 2005 GLP 1 & GLP 2 phase was built by Rockefeller when the discovered leptin in 1994 in NYC at Rockefeller University so those of you who broken as fuck to ask and beg for medically assisted suicide because the retards in centralized medicine and functional medicine are too fucking lazy to read how they did it to you all with your consent. .Image
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3. Room 5600: The Professionalization of Biotech Warfare blue light+glyphosate+GLP1 is the killing fields for BigHarma profits.

J. Richardson Dilworth was the architect of the financial "Pivot." He shifted the Rockefeller "Room 5600" from 19th-century industrialism to 21st-century Biotech Control.

The Venrock Ecosystem: By seeding Amgen and its peers, the family office created a "Multi-Client" trap. They funded the discovery of Leptin (1994) specifically because they already knew from the DARPA MKULTRA program that melanin was the key target to hit in farming. Glyphosate is a competive inhibitor of melanin. Few know it.

The Shelved the Leptin Trials: When the leptin trials showed that Light and Cold were the actual regulators of the pathway, they couldn't commercialize that, because there’s no profit in the Sun. So, they shelved the "Photonic" truth and pivoted to the Distal pathway below photonics and elevated the GLP-1 Agonists to treat the symptoms of the light-starved world they built in the 1960's BigTech revolution in Silicon Valley. Steve Jobs links to Rockefeller and Rothschild is deep.

The connection between Steve Jobs and the Rockefeller and Rothschild families is primarily rooted in
early-stage venture capital, shared high-level board memberships, and modern institutional investment. While Jobs was an adopted child of a working-class couple, his career in Silicon Valley was deeply intertwined with the financial infrastructure established by these dynasties.

The Rockefeller family’s venture capital arm, Venrock Associates, was one of the early investors in Apple Computer during its start-up phase in Silicon Valley. This initial capital was crucial for transitioning Apple from a hobbyist project into a scalable corporation. Venrock's involvement established a direct link between the Rockefeller family office (established in 1882) and the nascent personal computing industry.
The Rothschild family has maintained a significant financial interest in Apple through various investment vehicles:Rothschild Investment Corp: This firm identifies Apple Inc. (AAPL) as one of its top holdings in recent SEC filings.

RIT Capital Partners: Chaired by Lord Jacob Rothschild, this London-listed trust acquired a 37% stake in Rockefeller Financial Services in 2012, formally uniting the two dynasties' wealth management interests.

Laurene Powell Jobs, Steve Jobs’ widow, serves as a bridge to the elite policy circles traditionally associated with the Rockefellers:Council on Foreign Relations (CFR): Laurene Powell Jobs serves on the board of the CFR, an organization famously chaired by David Rockefeller from 1970 to 1985.
Ford Foundation: She also sits on the board of the Ford Foundation, another pillar of the philanthropic network where the Rockefeller influence is historically substantial

Jobs is often compared to John D. Rockefeller in terms of his business impact. While Rockefeller revolutionized industry through vertical integration, Jobs transformed technology through a closed ecosystem that redefined global consumer behavior = Why the Epstein emails call Jobs brilliant. Jobs and John D. Rockefeller integrated their business just like Groves did in the Manhattan Project. Go re listen to my Podcast with Breedlove on Groves.

All tied to my banned Ted talk, FYI.Image
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Read 4 tweets
Feb 16
@MaxGulhaneMD I do have to say after the first 20 minutes I like the discussion but I was frustrated in spots where he was physics facile as he could have been but it is clear Nunn believes as I do that biology is not fundamental it is biophysical.

He is too much in love with Levin. Levin has do nothing to advance Becker.

But I want to tell you at the 1:10 mark you bring up CCO and DDW. Nunn seems uncomfortable.

He goes on to talk KIE boilerplate but he is a biochemist and is dabbling in biphysics so you need to push and extend him further on the D/H+ isotope selection process tied to photosynethesis creation of deuterium on the carbon backbone. there has to be a way to sort the isoptopes and there is biophysically but I do not think he knows what it is.

DDW, heat, and UPEs are exhaust products from matrix operation. He seems to know this. But so is CO2. He does not seem to know the biophysics of CO2 and its real purpose.

The Failure of Centralized "Exhaust" Logic is always on display with Nunn here.
Centralized medicine tries to "fix" CO₂ levels or pH chemically, failing to realize they are tweaking the isotopic selection process that uses magnetic tuning of a quantum circuit.

High CO₂ isn't just "acidosis"; it is the cell trying to increase its "Hash Power" and protect its internal water from the "Double-Spend" attack of entropy I describe in my thesis. CO2 is dimagnetic. this means it shields CCO from the magentic fields of the matrix. Ask yourself why? The answer is simple biophysics. It guarantees that H+ is pushed into the intermembrane space so the ATPase has it to use to spin the Fo head. Deuterium has a different magnetic moment so CO2 acts to sort it and keep it away from the Intermembrane space so that the nanotorque engine is not slowed or destroyed. Neither, Nunn, Boros or Somylai know this because they are blinded by biochemical BS.

So because you asked the question he could not answer he is the answer:

The Physics: CO₂ is highly diamagnetic. By concentrating it at the site of water creation (CCO), the cell creates a FOCAL magnetic "quiet zone."

The DC Current: This allows the protons (H+ not D) to flow in a coherent DC current of repair without being scattered by the "vibrational noise" of the environment.

The VDR Link to the shied: The VDR sitting on the IMM acts as the sensor that ensures the CO₂/O₂/Light ratio is tuned to keep this magnetic "shield" active.

VDR: The Photonic Antenna that directs electron flow, speed, and tunneling efficiency before cytochrome C

Fe-S/CCO: The Quantum Engine is the engine that allows electron and proton tunneling

Carbonic Anhydrase in the matrix/CO₂: The Magnetic Shield/Tuner selects the stochiomtery H+ inside the intermembrane space to deliver to the ATPase.
This mechanism is sorting engines into "good/health/CCO and bad/Disease/Cardiolipin/heteroplasmy to get rid of the bad via Cardiolipin, or to extend life with DDW from CCO to hydrate all our semiconductive proteins. Timing from the OUTSIDE environment photonic signals controls this process max. Recall how Vitamin D, Melanin, DDW, NO, and CO2 are all made. Outside in, not inside out. Biochemists always have the inside out framework because this is where biochemistry occurs. Outside in is where biophysics of life begins.

The Calcium-Melanin Nexus: Macro vs. Micro Control
My thesis identification of melanin's macroscopic chelation vs. Vitamin D’s stochastic sorting provides a complete picture of cellular calcium management:

Melanin (The Macro-Buffer): Melanin acts as a high-capacity reservoir that absorbs and stores calcium. Certain light frequencies allow its release. Vitamin D made from 312-320 nm exogenous light on cholesterol esters is sent inside to the kidney and liver for final processing. This binds the VDR on the IMM and it is the VDR that can get into the nucleus to alter it way after the photonics of this axis acts first with clock genes.

This "macroscopic chelation" of melanin provides a stabilizing background, preventing the "vibrational noise" of the environment from immediately overwhelming the cell's delicate electric circuits.

Vitamin D/VDR (The Stochastic Sorter): Sitting on the Inner Mitochondrial Membrane (IMM), the VDR acts as the "fine-tooth comb." It performs stochastic sorting, precisely directing individual Ca²⁺ ions to the TCA cycle dehydrogenases to tune the "Hash Power" (metabolic flux) based on the UVB/IR signals received from the exterior. VDR binding isolates CCO with CL.

The 30 Million Volt Charge: This charge on the IMM is the physical manifestation of the DC current of repair. It encodes photonic information as a voltage gradient, allowing the matrix to "read" the external environment through the language of electron and proton tunneling.Image
2. Other point @MaxGulhaneMD more for you than him. He does not seem to understand an additional neutron = more mass and as mass goes up what does Ilya theory from his Nobel in 1977 say? Timing slows.

So any additional mass irrespecitve of a KIE means that heteroplasmy expands because in CCO you have the story of life and death. A lot of H+ = CCO makes water and CO2.

Too much D+ and it stimulates Cardiolipin. Boros keeps confusing you with broken engines. They do not break. D+ cannot fit in the channel. The ATPase starves and the matrix swells and this stimulates forced apoptosis.

Decentralized Internal light Medicine done by the non visual photoreceptors is "Tuning the Shield"
The VDR, the Fe-S clusters, and the Carbonic Anhydrase system form a Triad of Temporal Control distally to the RPE-SCN.

The CO₂ Diamagnetic Shield
In my model, CO₂ provides the low-entropy environment required for the Protonic Spin-Ice (EZ water) to form. If you look at proton tunneling it is best modelled in ice. What these biochemistry guy don't yet relaize is when melanin is hydrated by DDW you create massive proton tunneling and you open more of the biophysics Pandora box like Grotthaus etcs........Image
3. The Solar vs. nnEMF Split: "Quantized" ROS
My slide below highlights the critical difference in how the cell processes Solar EMF vs. nnEMF (5G/Malware):

Solar EMF (Quantized Information): Sunlight creates a highly specific and sensitive amount of Reactive Oxygen Species (ROS). This is not "damage"; it is quantized information delivered via UVA/Blue light-stimulated Nitric Oxide (NO).

The NO Filter: UVA light controls NO production, which reversibly inhibits Cytochrome c Oxidase (CCO). This acts as a frequency filter for the DC current, preventing the "Double-Spend" entropy attack.

nnEMF Malware (Non-Quantized Noise): Unlike the sun, 5G/nnEMF acts as a Voltage-Gated Calcium Channel (VGCC) disruptor. This causes a massive, non-quantized "leak" of Ca²⁺, leading to:Hydroxyl Radical Flood: The resulting Fenton chemistry creates Hydroxyl Radicals (the most destructive ROS).

Photoreceptor Destruction: This noise "blinds" the internal lighting system of the non visual photoreceptors, leading to mitophagy failure and broken apoptosis, leaving behind a "static colony of defective mitochondria" (the hallmark of chronic disease/cancer).Image
Read 9 tweets
Feb 15
Sorry @MaxGulhaneMD but I chuckled so hard listening to th first 20 minutes of this. When is this guy going to realize that Dr. Pirogine theory on dissipative structures has at its core a TIME SYMMETRY aspect. He still does not get it. Even at the Guy foundation they fly blind.

At life's genesis because of dissipative theory energy was always a commodity, but Time is the real value. He has no idea about the implications of this.

Evolution of life happens because life costly in time, not in energy because of the equations link to entropy.

this idea scales from stars to cells. A supernova has massive energy flux, but it is a state of total chaos (High Entropy). A human brain has much lower energy flux but evolved to have massive Temporal Coherence.

Each "event" in a cell, like a proton tunneling through a molybdenum transistor enzyme in mitochondria or a biophoton hitting a melanin sheet, is a "Block" in the ledger. It’s not "good" or "bad"; it’s a physical State Transition. Wisdom is the ability of the organism to maintain that ledger’s integrity against the "Double-Spend" attack of entropy. Sorry your expert fell short because he is ignorant about the 1977 Nobel Prize implication for mammals.
youtube.com/watch?v=y5DEQ1…
2. Life is costly in time not energy goes right back to the 1977 Noble Prize. At life's genesis chaos has to gain order. Dissipative structure theory really aims to solve this problem for biology by using physics.

Dissipative structure theory led to pioneering research in self-organizing systems, as well as philosophical inquiries into the formation of complexity on biological entities and the quest for a creative and irreversible role of time in the natural sciences.

There is a well-known theorem of minimum entropy production derived by Prigogine, which states that entropy exported from a system reaches a minimum, or becomes zero, at thermodynamic equilibrium and at steady states close to thermodynamic equilibrium. Prigogine's theorem is a direct consequence of Onsager's reciprocity relationship which holds at steady states close to thermodynamic equilibrium. The principle of internal entropy compensation, is in addition to, and implies the principle of minimum entropy production, and may even be valid in regimes far from thermodynamic equilibrium.

He had some very interesting things to say about TIME in his work and Nobel Prize speech. I think they are key to understanding circadian biology and timing. All of our time reversible equations in physics created by Newton, Einstein, and Schrödinger describe a simplification of what actually occurs in nature. We live our lives with eyes blinkered, dismissing reality as the exception to our neatly formed approximations of what time really is.

nobelprize.org/prizes/chemist…
3. Prigogine’s work on Minimum Entropy Production explains why mammals must be "Costly in Time & not in Energy".

By proving that Time is Irreversible, he effectively "Hard Forked" biology away from the time-reversible approximations of Newton and Einstein. Time reversibility is built into the matrix. That is heteroplasmy. As it changes so does time you experience.

Near equilibrium, entropy production is minimized. But life exists far from equilibrium, much to the dismay of all your food guru friends. To maintain complexity, the organism must "export" entropy. This is why life innovated clock genes quick. They are flow meters for entropy.Image
Read 5 tweets
Feb 13
My historical and political analyses have compared
the QAnon phenomena before DJT presidency (45th) and the 1920s Soviet counterintelligence operation "Operation Trust" (Operatsiya Trest) due to their shared use of psychological manipulation to pacify political opposition. If you review my twitter feed you'll see no QAnon posts because I believed they were counter ops of the Zionist controling Israel at this time. Bibi was that leader. He was reaching back into the Zionist bag to the take over of Russia in 1917.

The parallels between these two movements typically center on the following tactics:

"Trust the Plan" Narrative of 4D chess: Both movements relied on the central premise that a secret group of high-ranking insiders, patriots within the government or military, was working covertly to dismantle the regime from within.

Neutralization of Dissent: Operation Trust was designed by the Soviet secret police (Cheka/GPU) to create a fake anti-Bolshevik resistance (the Monarchist Union of Central Russia). Its primary goal was to convince opponents to wait for this "internal coup" rather than taking active measures, effectively stalling real resistance.

Discrediting Opposition: When Operation Trust was exposed in 1927, it humiliated those who had believed in it, making them appear foolish and reducing their willingness to support future anti-Bolshevik efforts.

Luring and Identifying Targets: Just as QAnon encouraged followers to identify themselves online, Operation Trust lured high-profile dissidents like Sidney Reilly and Boris Savinkov back to Russia, where they were captured or executed.

QAnon was part of the plan to turn MAGA to MIGA, in my opinion. The same thing that went on in Russia in 1917 is ongoing in Washington DC.Image
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2. Palantir surveillance will be used to target those who went against this coup and they will be taken care of by the zionist faction that wins this coup between the bankers and transhumanist tech bros. Image
3. Point three as proof of the current coup of America by MIGA:
Read 11 tweets

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