The amount of sleep an organism needs is directly tied to how well the organism deals with “entropy dump” back into its environment. If you do not dump it back into the environment well, you need to sleep more. If you dump entropy back into the environment well, you need to sleep less. No one has that understanding of the purpose of sleep because they do not have my understanding of how a quantum cell works. ----said by Moi, 15 years ago in a blog.
2. Each molecule of ATP in a cell controls 8800 water molecules binding sites and 20 potassium ions, to make metabolic water function as a liquid semiconductor inside every cell. I said this in the podcast 24 hours ago but wrote it in a blog 15 years ago.
A member on my forum recently posed the question, “we hear that ketones are a great brain fuel: they provide more ATP than sugars, burn cleaner, and may possibly be the preferred fuel, etc……….we also hear that ketosis works for refractory seizures and there are case reports and a few small studies showing benefit in autism, Alzheimer’s and possibly other neurodegenerative diseases. It appears most everyone reports sharper cognition and sense of energy/well-being. The confusing part for me is that many people also report poor sleep with ketosis. Why is just changing food, and no other variables, often linked to reports that their sleep worsens? It is a common complaint and I can’t yet make sense of it. Can you explain it to me?
Yes, this explanation came right out of a blog I wrote 15 years ago. Nobody seems to read anymore.
My Answer using Quantum Cell Theory: The answer to this is easy, yet complex, but buried in the science of the Energy and Epigenetics 6 blog post. When you eat a more ketogenic template you make more ATP to maximally unfold proteins. This is based upon the ability of one mole of glucose only making 36 ATP vs 147 ATP from the beta oxidation of fats. ATP’s main function in a zero entropy quantum cell, opens protein conformational structure to expose more water binding sites in proteins.
When this occurs the amount of ATP is stochastically linked to potassium concentration inside the cell. This is why potassium is found inside all cells and sodium is not. Sodium exclusion is not due to a membrane pump as most biochemistry books say. Gilbert Ling proved this mathematically and experimentally close to 50 years ago. The only reason his work was not accepted was because biology does not realize that energy in cells is generated by semiconduction of charged particles that are separated from water. Becker’s proof on Ling’s conceptual framework did not come until 9 years after Ling showed why K (potassium) and Na (sodium) are included and excluded because of the semiconducting currents found inside cells energized by sunlight. This has been further proven in the molecular actions of rhodopsin, melanopsin work in the retina, and actin and myosin in muscle by Gerald Pollack, all using hydrated protein semiconduction.
3. How does physics explain K+ ions and light and water? Brownian motion = statistical motions of atoms Einstein realized this the demon Maxwell was talking about in 1867. it took 38 yrs for someone to make sense of it. Do you know, of Einstein's 4 miracle papers of 1905 that the one on Brownian motion is the one most cited? Yet he won nothing for it.
Maxwell was the first to show that the second law of thermodynamics had to be statistical. Einstein showed Brownian motion was the observation of the statistical event predicted by Maxwell. In the 1950's science really upped this game when transistors and semiconductors were found. Why? any trap door that opens in one direction only and requires a specific amount of energy to open it is essentially a Maxwell Demon.
This gave birth to solid state devices we use today. Rectifiers let current pass in one direction and not in reverse, thereby converting AC currents to DC ones. In the 1960's Becker showed bone had a rectifying current built by light in periosteum. The implication is that these semiconducting gates can randomly convert a fluctuating current of electrons in a membrane into a DC current that can be used to physiologic work. The electrical potential of the cell membranes stores energy of light in the electrons it captures photoelectrically. This is done by Coulomb's law. Membranes are designed to capture electric flux and captures magnetic light flux. This, in turn, excites the electron and it becomes a particle only and loses its wave ability. This is part of the photoectric effect. So an excited electron in a semiconductor can only act as a particle. A delocalized electron has more range to act differently, as a wave and/or a particle.
This idea leads us to one conclusion: the electrical potential difference between two sides of a membrane can be harnessed and used to perform cellular work when ever it is needed. Why can energy be harvested in life anytime it wants it? The photoelectric effect is instantaneous, therefore time is no longer an issue. Photons never experience time, unless they are catured by a semiconductor. Even then, they are moving fast just not at the speed of light. The speed of light in a tissue is the rate limiting factor for a cell.
A calculation shows that the electron is traveling at about 2,200 kilometers per second. That's less than 1% of the speed of light, but it's fast enough to get it around the Earth in just over 18 seconds. In silicon (Si) the electron mobility is of the order of 1,000, in germanium around 4,000, and in gallium arsenide up to 10,000 cm2/(V⋅s). Hole mobilities are generally lower and range from around 100 cm2/(V⋅s) in gallium arsenide, to 450 in silicon, and 2,000 in germanium.
Inside your wall copper slows electrons down big time. In the case of a 12 gauge copper wire carrying 10 amperes of current (typical of home wiring), the individual electrons only move about 0.02 cm per sec or about 0.5 inches per minute (in science this is called the drift velocity of the electrons.)
What else is key in this understanding? You begin to see why all eukaryotic membranes are loaded with DHA that have 22 carbons with a huge amount of "electron holes". These holes allow for electrons to delocalizes rapidly. They contain pi electron clouds that are waiting to be excited by incident light from the sun to store this energy for the cells use later on. This explains why DHA has never been replaced one time in 600 million years of eukaryotic evolution, even though evolution is about change over time. Why is it a thermodynamic constant for eukaryotic life? It liberates electrons rapidly to move light energy at rapid speeds. In fact, it is the only lipid capable of turning sunlight into a DC electric current and a DC electric current back to light. What does the high DC electric charge in the inner mitochondrial membrane release when this charge is stored at the electric and vibrational level in a the mitochondrial of a cell? Water. Water than is devoid of deuterium. Water that is designed to operate like a semiconductor. What is its connector to water? Potassium ions are that answer. K+ ions act like glue does in hydrated molecules. K+ is s special when it is married to water and light from the sun hits it. It raises the Coulomb force in youre semiconductor factory called a mitochondria.
4. ^^^^This post above and the podcast linked above tell you why I do not respect Ray Peat and why he and his lemmings never understood Gilbert Ling's real brilliance. Decentralized science improves via centralized funerals. Max Planck was right.
5. Let us take two chronic diseases that centralized medicine has NO ANSWER FOR.
HOW ARE Parkinson's Disease AND FIBROMYALGIA THE SAME BUT DIFFERENT? Both come from a lack of light at a particular surface. = PD = lack of dopamine in the RPE, leptin melanocortin pathways and then it hits the substantia nigra and melanin vanishes.........this is why Parkinson people lose, their tans, have a higher incidence of skin cancer, lose muscle mass and it even causes their special non expressionless faces...........PD is usually related to a lack of full spectrum sunlight getting to the eye to build dopamine, melatonin locally in the retina. They have a deep need for melanin renovation in the SKIN/brain.
If the eye doesn't get the stimulus of UV/IR light neither does the frontal lobes nor the brainstem = substantial nigra = PD.
What happens if you live your life 99% indoors and always around fake light always covered up with clothes or fake light? Fibromyalgia = skin surface defect = this implies PD and FM are somehow linked in quantum fashion doesn't it? HOW? Where does skin and brain come from in a zygote? NEUROECTODERM.................BOOM. Have you ever seen any FM with a tan? Most of them have hypothyroidism too. Guess why? Slides below shows why.
6. DETAILS related to the quantum mechanics in cells: When water in your cell can not carry the right amount of energy life can not grow. Cactus does not grow in the Tundra do they? You are more complicated house plant. Think of a plant. If a plant has little water and lots of sun will it grow and live well? No. If your mitochondrial do not make water be healthy or suffer from a chronic disease like PD or FM?
Realize water and the level of potassium (K+) in a cell are linked. Energy is tied to K+ ion concentrations and this is connected to ATP levels at cytochrome 5, the ATPase. K+ also links to water molecules and in turn to ATP molecules stochastically. For every 0.3 mEq below 3.8 mEq that potassium is on a standard blood lab draw, means there is 100 mEq deficit of potassium INSIDE a cell.
7. This deficit cause a mitochondria to consume more calcium and it swells. This slows ECT because it increases the distance of the respiratory proteins. The atomic size change altered the local geometry below your skin where your muscles are. Why? The Coulomb force loses it power as scale changes. This is where muscle pain and FM come from. This is linked to the redox potential in a cell (amount of UV light confined) because it is linked to the electrostatic attraction in a cell. This is huge for potassium, because its K+ ion has the unique ability in “gluing of water”. Gluing = EZ of Pollack or the AI hypothesis of Ling = coherent domains of quantum cell theory. Potassium ions are able to glue water because the ion's atomic radius allows it to polarize in sunlight. Sunlight is normally unpolarized..............K+ ions is the initial polarizer of sunlight inside cells. When somebody is in an environment that causes the dielectric constant of water to lower from 78 for any reason (LOTS IN MODERN WORLD), the polarization of the ion becomes smaller than cell water. This cause a huge electric problem (collapse) in the cell because polarization energy of K+ is subtracted from Coulomb energy.
8. Normally K+ is more polarizable than water, so polarization is added to the Coulomb energy in a cell. When fluoride or bromide, from toothpaste, grains, or skittles are present in you, for example, are added to a cell dielectric collapse occurs. Sunscreen does it too. So does make up ladies. Kim Kardashian's ideas are bad for your skin and brain.
This is precisely how the dielectric constant in water is destroyed. In the normal state of affairs in wellness in the sun, this allows potassium to function as the optimal "photo-electrical adapter" to transfer energy throughout the cell coherently. It is also massively important in patients with dielectric collapse because intracellular dehydration from non native EMF completely ruins this relationship and this is why they find it so hard to get better fast. ATP is designed to unfold proteins fully to open their carbonyl and imino side chain groups on all amino acids to intracellular water. This action allows binding and polarization to separate water into subatomic particles that are positively and negatively charged.
This action is called building or expanding the exclusion zone (EZ) of water. Dr. Gerald Pollack's experiments showed these effects. Dr. Gilbert Ling proved by experiment that each molecule of ATP in a cell controls 8,800 water molecule binding sites and 20 potassium ions to allow water to become structured inside every cell of your body. The first step in photosynthesis and in mitochondrial oxidation/phosphorylation of electrons is to charge separate water...........now you know the why K+ and sunlight help muscle pain and fatigue reverse. UV and IR light build dopamine and melatonin which stimulate muscle growth and entrain properly function by maintaining the respiratory proteins in muscle mitochondria. Light is the most powerful drug we have.............especially for muscles. Get some sun.
9. Water polarization:
10. Potassium needs to stay bound tightly within cells in order for intracellular water to remain structured to maintain semiconduction. When potassium is released water loses its structure and you rely on the ancient evolutionary system of the ATPase, lowering your margin of safety in disease avoidance.
11. You might recall that mitochondria are filled with H+ ions in its matrix. Do you know why H+ was chosen? The deep reason was mass equivalence and its relationship to thermodynamics. Hydrogen is the lightest atom making it an ideal semiconductive component to move energy at low thermodynamic cost.
Hydrogen is the other side of the equation for water and for life. It is special in its own way. Hydrogen is a gas found in the atmosphere at trace levels which can not sustain life. It is synthesized from hydrocarbons and water.
Hydrogen gas makes up the lightest fraction of the H2O molecule. Hydrogen is both the lightest and most basic of all elements, to most scientists.
I don’t see it that way. Hydrogen is the most complex of all the elements because of what it can do in an altered environments. It is a fairly reactive gas, which enters into chemical combination with most of the elements and is feebly repelled by magnetic forces. This is why the ATPase spin rate does not affect its behavior.
When hydrogen is ionized or charge separated, however, what can happen in life at the cell level changes in a big way.
This is when hydrogen becomes the superman of flow. When hydrogen is ionized and loses its only electron it becomes a proton cation. This makes H+ the lightest cation in chemistry and given small size of the proton, explains the unusually high diffusion rate of the proton relative to that of other common cations like potassium (K+).
When hydrogen loses its electron is becomes an ionic plasma that begins to act like a liquid metal. This makes it the ideal semiconductor. Ionic plasma’s have special abilities. One ability is called proton jump conduction or protonicity. These rules are governed by something called the Grotthuss mechanism.
12. Hydrogen is a chemists conundrum, a biologists enigma, and biophysicists dream because it can lose or gain its single electron by delocalizing it. I have always been of the belief that hydrogen did not really belong to any group in the periodic table based upon this ability. Hacking the periodic table is something a decentralized clinician must be adept at.
After many thoughts on my table hacks, I realized under some environments it can be placed into group 7 or group one in the periodic table. All known elements of group 7 are halogens. The group 1 elements compromise the alkali metals. Hydrogen is often placed in group one of the periodic table by convention due to its electron configuration, but it is not considered by many to be an alkali metal. Why?
Hydrogen rarely exhibits behavior comparable to that of the alkali metals. For example, all the alkali metals react with water, with the heavier alkali metals reacting more vigorously than the lighter ones.
The word “alkali” received its name from the Arabic word “al qali,” meaning “from ashes”. These particular elements were given the name “alkali” because they react with water to form hydroxide ions, creating very basic solutions (with pH > 7), which are also called alkaline solutions.
Hydrogen forms water with paramagnetic oxygen directly and does not form a basic solution. Adding more hydrogen to it does not cause a special reaction at all, as it does with the other metals in group 1. Why is hydrogen fundamentally different?
13. Water is most famous for forming hydrogen bonds with other water molecules and with other ions dissolved in it. A hydrogen bond consists of a hydrogen shared between two electronegative atoms like oxygen or sulfur. The compound that donates the hydrogen to the chemical reaction is the hydrogen donor, and the acceptor atoms is the hydrogen acceptor.
Water is unique because it can be both an acceptor and a donor of hydrogen. It means water can be a switch hitter in many biochemical reactions.
This is why water is the universal solvent on Earth. In fact, water can even donate two of its hydrogen’s if need be. This makes the water molecule take on the tetrahedral structure in its frozen form linked in a crystalline hexagonal array in crystal ice.
14. I told you hydrogen can also act as a group 7 halogen. It means it can gain electrons to become a non metal. It takes on interesting properties when it acts a a non metal in cells. When hydrogen does this in water when it is associated with iodine it forms an ionic liquid.
Ionic liquids are now receiving special attention in science, owing to their unique properties such as high ionic conductivity, non-volatility and non-flammability. This ability makes these fluids versatile alternatives to conventional solvent-based systems used to make batteries, fuel cells, and super capacitors that hold large charges.
They are also quite helpful as heat-transfer fluids to move infrared energies within a system. Iodine addition to iodide-based ionic liquids leads to extraordinarily efficient charge transport, vastly exceeding that expected for a standard viscous system. This is why your thyroid gland uses iodine in T3 and T4. The numbers correspond to the the atoms of iodine doped tothe aromatic amino acids tyrosine/phenylalanin in the top pathway seen below. Most biochemists like Ray Peat had no earthly idea why thyroid hormones and melanin were linked. Peat talked about thyroid hormones and temperature but he had no idea about how neuropsin and mTOR fit into this pathway. Much less how it worked. His myopia lead him to suggest eating carrots, OJ, and cola loaded with sugar was wise because it drove thyroid hormones. None of this was true without the light needed to drive this pathway.
15. Hydrogen and iodine form an ionic plasma within CSF of the human brain. The choroid plexus of the human brain is designed to add iodine to CSF. CSF, you will recall is an ultra-filtrate of blood plasma and is made up of 99.9% water.
When iodine meets water that has been charged separated by UV and or IR light or by the hydrophilic proteins within the dura matter a massive amount of H+ is made in the CSF of the brain.
Using the Grotthuss mechanism, iodine is able to move protons closer together than we would normally expect, to alter their hydrogen bonding network to allow them to form superconducting proton cables that act like a positive charge electric current. The higher the current the more your temperature varied and vice versa. This affected your coupling ability irrespective of your haplotype.
The mechanism allows for electric and mgnetic charges to be transported not by the movement of particles, by the breaking and reformation of chemical bonds. As water is charge separated by endogenous UV-IR light production or by hydrophilic surfaces, many excess H+ ions are made adjacent to these surfaces in water. This created a coherent domain in water filled with electrons that could be powered up by light and delocalized in the cells for use at anytime. Gerald Pollack’s experiments have shown this ability to some degree. His work needs to be extended to water devoid of deuterium to see its full effects.
Why? In DDW excess protons can diffuse through the hydrogen bond network of water molecules or other hydrogen-bonded liquids (iodized CSF) through the formation or cleavage of covalent bonds. This alters biochemistry in ways a biochemist is clueless about.
16. Grotthuss was the first correct concept for the charge transport in electrolytes, and it still remains valid for the charge transport in water. It allows for protons cable construction within an ionic fluid by using a current of protons (H+) that use a hopping mechanism.
That hopping mechanism is referred to as quantum tunneling of protons. Hopping is more efficient the closer H+ protons are to one another.
Quantum tunneling becomes more probable the smaller the mass of the cation is, and since the proton is the lightest possible stable cation on Earth it is Nature's ideal choice for proton semiconduction. Iodine and iodides turbocharge this ability by turning the sea of protons into an ionic plasma. This is why the thyroid gland, human breast, choroid plexus, and intestinal gut lining all concentrate iodine and iodides and H+. Women with lumpy breasts are pale and lack iodine and very prone to breast cancer.
17. The dipole nature and propensity for hydrogen bonding are why water has an unusually high dielectric constant of -78 at room temperature. You’d be wise to remember this fact. This makes it the most polar solvent in all of chemistry and biology! This fact alone should have gotten biochemists attention that intracellular water is really critical, but it has not.
Why is this a big deal? In QED and semiconduction, anything with this high a dielectric constant becomes easily polarized by an electric or magnetic field in light.
18. Both of these things happen in the human CNS and in our mitochondria.
This is why the quantum magic can happen between electromagnetic radiation and forces with water. This is why our biological semiconductors are built with hydration.
So which is more suitable for hydrogen?
It turns out how hydrogen acts chemically, depends upon the environment it is within. Does this means hydrogen can take different forms in our body if the environment of that region is controlled by information in some way? Is it a donor or a collector of electrons? Is it a metal or a gas? Science depends on compelling narratives, and few people seem to the know the real story behind hydrogen. Above I showed you how hydrogen can act as a metal or non-metal. Hydrogen makes life a cooperative quantum dance and it can make other elements do things they normally would not do.
This is why hydrogen always hangs out with carbon and oxygen in life on our planet. The hydrogen ion (protons) and electrons go to reduce (or fix) carbon dioxide into the carbohydrates and biomass of photosynthetic organisms using both the C3 or C4 pathways, which feed herbivores, and down the food web, the vast majority of animal species. The air-breathers break down carbohydrates by oxidizing them (with oxygen) in the mitochondria of cells to obtain energy for growth and reproduction, regenerating carbon dioxide and water. This completes the living dynamo of photosynthesis and respiration that turns inanimate substances into living organisms via photolithography using sun light and hydrated carbon based semiconductors. mdpi.com/1099-4300/16/9…
19. Hydrogen is the rogue element in the periodic table that breaks all the rules we expect, and this is why life uses it in her designs. When a hydrogen bond forms between two water molecules, the redistribution of electrons changes the ability for further hydrogen bonding. In this sense, a hydrogen bond can be electrostatic. Hydrogen bonds, however, can become covalent as well. Iodine’s addition to hydrogen favors the formation of covalent bonding in water.
This is a fancy way of saying hydrogen makes other atoms do things they normally might not want to do. Hydrogen’s will is strong because of the closeness of its one electron to its nucleus.
This gives hydrogen lots of different isotopes. It also means hydrogen invokes Einstein’s relativity theory more than any other element on the periodic table. You might not understand why now just yet, but I cover that here in DETAIL. optimalklubs.com/kruse-for-dumm…
20. Hydrogen normally has one proton that is encircled by one electron that buzzes in its electron shell. Its valence shell is designed to hold two electrons. So you need to ask yourself is the shell half filled or half empty? Other atoms want to know this too because this is how they decide how they react with hydrogen. This is why hydrogen can be a chameleon. Most elements either gain or lose their electrons in chemical reactions. The pathways that hydrogen electron takes determines the chemical abilities of the atoms in this dance. Hydrogen swings, either way, depending upon the environment it finds itself in. This makes it a very interesting player in biochemistry. It’s no wonder hydrogen is an integral part of life’s plan. Hydrogen is found all amino acids and protein polymers. It also makes up 2/3 of water which makes up your semiconductors.
Elements that lose electrons tend to be metals (H+). Elements that gain electrons are non-metals. Hydrogen can be both and do both extremely well sometimes within the same ionic fluid. This is what makes hydrogen special. However, hydrogen roams determines where life goes and what it is capable of. Hydrogen is a fundamental “symmetry breaker” of all condensed matter in us or in the universe. Hydrogen gives water its special abilities. Life can not exist without hydrogen or its parent, water. Remember, the mitochondrial matrix is filled with H+. Don’t forget this point.
21. A biologic cell is a dissipative system by its very nature. This implies it has the role or purpose to break symmetry and create a metastable system to react to all environmental possibilities that the cell may face. A cell uses hydrogen and oxygen to un-condense our protein polymers, ever so slightly, to allow life to exist. When we sleep we are designed to be fully condensed. This implies that life can only exist when our protein polymers are slightly unfolded. This unfolding happens when electrons are withdrawn from proteins. Cortisol and ATP are electron withdrawing chemicals.
Cortisol is linked directly to POMC and the solar light and dark cycles.
Gilbert Ling was the first scientist to realize what ATP did to proteins. ATP allows for amino acids to unfold to allow for water binding sites to open to the water hydration shells around proteins. When we are awake our proteins have to be somewhat unfolded and un-condensed. This is why I told you in Cold Thermogenesis 2 that I believed that life primordial condition was sleep. I believed we evolved wakefulness when we gained the ability to unfold our protein polymers.
22. Similarly, a cell is designed to break symmetries in semiconductive circuits by using the biophysics buried in the atoms of hydrogen and oxygen to its advantage. This ability must be associated with a specific molecule capable of breaking symmetry. H20 can “unfold” or ‘charge separate’ into H+ and -OH with the addition of UV light and/or infrared heat from the sun or when it lies adjacent to hydrophilic substances.
Did you know proteins are made more hydrophilic with the addition of electrons to them. Did you know ATP and cortisol move electrons to and fro in water to change how proteins fold? They are made more hydrophobic when electrons are removed. It turns out all proteins are hydrated in life. Our proteins are the first smart device ever built by nature. Proteins are semiconductors. They have an electronics built into their structure. Albert Szent Gyorgi was the first person to understand this in 1937.
In my opinion, this is why DNA only codes for protein. It creates the semiconductiove backbone critical to the electronic state of life under our star.
When we die we lose that ability and our muscles get hard in stiff in rigor mortis. Liquid water is the perfect chemical to break symmetry with all the semiconductive protein polymers in all life forms. The reason is found in water’s molecular 3 D molecular arrangements. Liquid water has perfect symmetry in that no matter from which direction you look at the molecules, the view is the same from a molecular standpoint. But water, can and does, lose its symmetry in nature naturally.
23. Symmetry is broken by any phase transition in chemistry. Any time symmetry is broken, energy and information transfers must occur by nature’s laws. This occurs many times in biochemical reaction of cells. And as such, all breaks of symmetry require a transfer of energy by the laws of physics to satisfy the Second Law of Thermodynamics. Symmetry is also broken any time temperature rises or falls or when electrons or protons are moving in any biochemical reaction. Any transfer of energy/information has the potential to break symmetry and therefore to give rise to emergent properties in the protein polymers or products of these reactions.
The line between metal and non-metal status in any element has become quite blurred because of hydrogen. Physics is now awakened to this issue. This is a new problem for modern chemistry. Its implications have not yet been appreciated by biology. When you consider that hydrogen is involved in most biologic reactions, this has massive implications for the biology of you and for life in general.
24. When I was a student growing up, hydrogen had a clear distinction in chemistry. Sodium and hydrogen are group 1 elements. Not only is hydrogen capable of switching teams, so is sodium its neighbor.
Sodium is also used by life in a big way in extra and intracellular ionic fluids. Now we know that hydrogen and sodium “switch teams” based on their local environment. When the conditions of existence in these atoms environment is altered, they can change their chemical abilities. This action seems very counterintuitive, yet it has been proven by experiment. This makes them “metastable atoms”. Life appears to like to use atoms that are cationic, small, and metastable. This creates the most possibilities for life in biochemistry.
25. Sadly, biochemists do not see this realm in their equations in their books.
Why do I say this?
We all think hydrogen is a clear gas. But on Jupiter, hydrogen is under so much pressure with an altered temperature, it becomes an extraordinary superconducting metal. In mitochondria, H+ becomes a metal like plasma as well. MEG data shows that the two tissues with the highest mitochondrial densities have large magnetic fields, namely the brain and heart. This is why Jupiter is believed to have a stronger magnetic field than the sun. Hydrogen gas is diamagnetic on Earth while its dance partner gas oxygen is paramagnetic. One repels a magnetic field while the other is drawn to one. So hydrogen acts differently on both planets because each planet fosters a different environment.
In space, hydrogen also acts differently magnetically. Hydrogen is a plasma in space. When air or gas is ionized, it loses its electrons and plasma forms with conductive properties similar to those of metals. Plasma is the most abundant form of matter in the Universe because most stars are in a plasma state. Heating a gas may ionize its molecules or atoms by reducing or increasing the number of electrons in them, thus turning it into a plasma. A plasma contains charged particles: positive ions and negative electrons or ions. I’d like to remind you here that your mitochondrial matrix is filled with H+. This is a hydrogen proton missing its electrons. Mitochondria also liberate light in the form of UV and infrared light/heat. It too acts as an ionic plasma in you.
26. Magnetism is the essential force that determines the form of plasma or ionized matter takes in an environment. Recall that all free radicals in mitochondria are magnetic molecules. They are this way because they have unpaired electrons. This affects how water behaves in your semiconductors. This is how mitochondrial ROS/RNS alter semiconductive pathways in your cells. Your central retinal pathway is one such item.
The hydrogen regions around galaxies are also considered plasmas, despite their degree of ionization being small. The degree of ionization in interplanetary space varies between unionized states or can morph to fully ionized states in other regions of space. In space, however, even the weakly-ionized plasma in the hydrogen region reacts strongly to electromagnetic fields. Magnetized plasma, such as contained in the hydrogen region, is the dominating state in the universe as a whole. Our sun produces massive amounts of plasma it spits out at us into the solar system as the solar wind or a coronal mass ejection. The sun’s plasma is contained by the high electric and magnetic fields of the sun.
Might this ability also be present in our mitochondrial matrix? After all, H+ is contained by high electric charges and magnetic fields in mitochondria as well? YEP
27. When pressure and temperature bring electrons so close they have to begin to occupy spaces that minimize subsequent repulsions. This action will not allow the electrons to roam free as they are used to doing in an aqueous solution. When you control the action of electrons and allow protons to roam free in a liquid plasma, you really are seeing “the wand” of the cosmic creator at work.
E=mc^2 is the wand. Mass eqivalence however sets the stage.......for more quantum magics to happen in you below your ability for the biochemistry book to explain it to you.
28. Did you know free radicals like ROS and RNS slow down or speed up electrons in you?
How?
So how does Einstein’s relativity directly tie to this short narrative on hydrogen? Einstein’s relativity theory allows for space and time bending. It also bends the mind of many people who look deep enough to see how far-reaching his ideas go. It turns out relativity has a major effect on the elements of the periodic table.
When we get to an atomic mass of 79 we begin to see the counterintuitiveness of his ideas. Most of us know gold stands out in the metals on Earth because of its color.
Gold has its special color because of Einstein’s relativity. I bet you have not heard that before. When we get to the atomic number of 79 the highly charged nucleus the innermost electrons only move at 80% the speed of light. This shows you that atomic mass has an effect on electrons. Gold’s electrons have slowed down relative to platinum which is adjacent to gold on the periodic table at atomic number 78.
When electrons slow down, this actually increases their small mass by the mathematics in the mass equivalence equation above.
is why magnetism also slows electrons down. Here we see a thermodynamic problem that must be solved. This small change causes the innermost electrons to get closer to the nucleus than usual. The longer range effect of this shields the outermost electrons from the pull of the nucleus. This causes the outer shells of electrons to expand outward. Here again, you see when electrons energies decrease, mass increases. This topic should raise the question, what happens to hydrogen when a single neutron is added to its sole proton and electron? Does something unique occur? It does. Its magnetic moment changes and this slows electrons down further. This is why deuterium is used in coherence creation.
This is the relationship I mentioned to you in the EMF 2 blog post showing up, yet again. As the outer shell extends and expands, all the normal quantum connections of how electrons fill their shells begin to break down.
This quantum effect in gold is seen directly by the naked eye when we see its color compared to the gold’s neighbors who have a white grey color. In hydrogen, the effect is not seen by us but it is felt in places where hydrogen is located.
When light hits gold the wavelength effects on gold’s outermost electrons is altered. It causes metallic gold to look a lot different than the elements that are around gold on the periodic table (platinum or mercury).
Gold is the color gold because of a wavelength shift of light by its outermost electrons. This is a quantum effect of its electrons. Mercury is a liquid for the same reason. Do your experts know any of this decentralized science buried in Nature?
29. What does this issue reflect? You need to understand Einstein’s relativity to fully appreciate the long-range implications for biology. It also turns out that this is why the metal mercury is a liquid at room temperature. The low melting point of mercury is also due to Einstein’s relativity. Peter Schwerdtfeger at Massey University just proved this in 2013 to small fanfare. Why am I telling you this detailed story about atoms and electrons?
Because hydrogen can control the flow of electrons and that control arm actually controls the chemistry of water. That in turn controls the electronic state in proteins using quantum effects of its electrons. This is how you work. The books are wrong.
30. It turns out these long-term ideas are dead wrong and most of the biochemistry is based on these ideas. This is a big deal in chemistry and physics right now. There are a couple of red herrings in nature’s design and the theory of relativity is one of those red-herrings. This showed chemists in 2013 that there is certainly a limit to the periodic table but science has no idea of where those borders are today. This was music to my ears and it will be really bad news for today’s biologic dogma. I am not sure when biochemists will realize the massive effects of these findings.
My prediction will be that soon physicists will be dictating the new laws to clinicians of how biochemistry can act instead of the ideas put forth by modern biologists. The biologic ideas and constructs of life are built around a stable periodic table of atoms. The periodic table is no longer considered stable by physics because of these effects.
This means that atoms that makeup living things can be altered directly by physical changes without the interaction of another element in a reaction. Hydrogen, sodium, and potassium are some of the smallest cations used in biochemistry and them manner in which they can turn into an ionic plasma with iodine are massively important to how life is powered. It also points out why biochemistry can occur without two atoms interacting in a molecular reaction. Biochemistry is not the only way life can adapt it appears based on these findings. What it also implies is that we no longer can predict detailed properties of things made from atoms that can swing multiple ways. I’d say that is a pretty big deal in the world of science considering all amino acids and proteins have hydrogen in them while they float in a soup of water, sodium and potassium and iodine.
So why is this narrative important for you to understand?
31. Hydrogen is tied to every amino acid and it makes up the largest portion of water. Your topologic insulators/semiconductors are also made from both of these components. Your mitochondrial matrix is filled with hydrogen protons and surrounded by water. To fundamentally understand life you must understand hydrogen’s weirdness.When any part of this thermodynamic equation changes the physiologic abilities of the topologic insulators also change. Hydrogen is a rogue element that can alter the chemical basis of proteins coded for by DNA. Hydrogen bonding alters the atomic relationship between atoms to fully unleash the power of atomic chemistry for life to organize around. The anomalous properties of liquid water may be explained primarily on the basis of its hydrogen bonding alone. I spoke about them here before.
Now you have the full picture why I think all biochemists need to be shunned. None of them know this science. I know because I present Ray Peat with most of it and he said this was a "comic book idea".
I chuckled and now I chuckle at his disciples.
32. IMPLICATIONS OF PEAT's MYOPIA?
Most people are also unaware that a hydrogen bond is tied to the electromagnetic force naturally. The reason is that the hydrogen bond is the electromagnetic attractive interaction between polar molecules, in which hydrogen (H) is bound to a highly electronegative atom, such as nitrogen (N), oxygen (O) or fluorine (F). In water’s case, that atom is oxygen. The name hydrogen bond is something of a misnomer, as it is not a true bond but a particularly strong dipole-dipole attraction, and should not be confused with a covalent bond. Water can contain many covalent bonds as well if its environment is entrained to make it happen. You saw the importance of covalent bonds with respect to the Grotthuss mechanism mentioned above.
WHY THE WEIRDNESS IS IMPORTANT= IT FORMS THE IONIC PLASMA IN MITOCHONDRIA THAT LINKS THE INSIDE WORLD TO THE OUTSIDE WORLD
When a hydrogen bond forms between two water molecules, the redistribution of electrons changes the ability for further hydrogen bonding. The water molecule donating the hydrogen atom has increased electron density in its ‘lone pair’ region, which encourages hydrogen bond acceptance, and the accepting water molecule has reduced electron density centered on its hydrogen atoms and its remaining ‘lone pair’ region. Cite one below gets into these details.
This action encourages further electron donation but discourages further acceptance of hydrogen bonds. This makes the hydrogen bonding network a chameleon for the transfers of energy and information. This electron redistribution thus results in both the cooperativity (e.g. accepting one hydrogen bond encourages the donation of another) and anti-cooperativity (for example, accepting one hydrogen bond discourages acceptance of another) in hydrogen bond formation in water networks. It can work together or not work together depending on the environment it is placed in. The hydrogen bonding network in water is about 90% electrostatic and 10% covalent. The covalent nature of the network is directly impacted by the amount of polarization of water by light. This is why the amount of light released by mitochondria is awfully important in wellness and disease states.
33. I told you in the podcast with Cameron Borg above just how important the Coulomb force was to life. It is the force that holds our biological semiconductors together in creating a proper AMO setting and they react and change via light and the fields and magnetic signals they get from mitochondria by ROS/RNS. This system is built with high fidelity. nnEMF or alien light ruin its fidelity. The physics of organisms is more important than the biochemistry they run. Why? The AMO physics controls how biochemistry happens.
34. Water can also become a gel plasma when it charges separated and interacts with sunlight. I would remind you that infrared light is released into the water surrounding our mitochondria naturally. The interaction of light with liquid water generates quantum coherent domains in water, where the water molecules oscillate between the ground state and an excited state close to the ionizing potential of water.
This produces a plasma almost free electrons favoring redox reactions; this becomes the basis of energy metabolism in living organisms. This is what I believe happens in human mitochondria. Light is thought of as always moving and never motionless. Light can be constrained by strong electric and magnetic fields. Moreover, in liquid crystals, photons can also become trapped and form its own crystal and fixed within the living matrix to fuel life’s processes.
35. This points out why the incorrect amount of light often leads to the wrong proton signals in water. You saw this revealed in the Multiple Sclerosis blogs I wrote years ago. It is also why we see protons spin abnormalities on MRI images in MS.
Here you can see where photon release from the mitochondria can directly alter the physiology of the hydrogen bonding network in water directly. I spoke about water and protein polarization in blog’s OSF 3 , 4, and 5. Changes in the hydrogen bonding network in water can lead to compliant design flaws in our protein polymers. Water also polarizes around proteins at all times and that action reduces the hydrogen bond length in that intracellular water to form coherent domains.
Coherent domains in water are designed to naturally trap electromagnetic frequencies from the environment to orchestrate and activate specific biochemical reactions through resonance matching. Water is a repository of the environment’s electromagnetic potential at all scales. This is how seasons are sensed and it is how all five of our sense work as well. This also happens to be why ionic plasma suspended in water are used in some form by every one of our sensory systems in our brain and peripheral nervous system. Water is how we decipher all environmental signals.
36. When we consider the quantum chemical calculations of the relevant inter-residue potential constants of amino acids we see a big difference. These are called compliance constants in protein chemistry. The calculations revealed large differences between individual hydrogen bonds of the same type. For example, the central inter-residue N−H···N hydrogen bond between guanine and cytosine is much stronger in comparison to the N−H···N bond between the adenine-thymine pair in DNA. So as the hydrogen bonding network changes so do the tightness or laxity of the double helix of nucleic acids. These changes directly affect DNA’s thermodynamic profile. They also directly affect its resonance and its oscillations. These resonant frequencies are what allow for nucleic acid expression. Luc Montagnierhas measured the EMF emitted from nucleic acids and all of them are in the low-frequency range. In 2009, Montagnier published two controversial research studies which, if true, would be the most significant experiments performed in the past 100 years, demanding a re-evaluation of the whole conceptual framework of modern chemistry. His work has now been repeated by independent labs to the consternation of many scientists. Why do his experiments work?
Cooperative hydrogen bonding increases the O-H bond length whilst causing a 20-fold greater reduction in the H····O and O····O distances. The increase in bond length has been correlated with the hydrogen bond strength and resultant O-H stretch vibrations. This allows for an easy donation of the hydrogen protons to form “excited water”. Dr. Montagnier experiments pull the veil back on how hydrogen works behind the scenes in water. He has unleashed the rogue side of hydrogen for all of us to see.
Excited water is the source of superconducting protons that allow for rapid intercommunication within the body that is associated with information transfer and energy transfers to power cellular work. Thus O····O distances within clusters are likely to be shorter than those at the periphery, in agreement with the icosahedral cluster model for water.
Why is all this complex scale of science important to grasp?
All memory and information transfer begins with the movement of the hydrogen bonding network in water.Hydrogen bonding carries information about solutes and surfaces over significant distances in liquid water. This information is transmitted by proton flows and resonant vibrations in liquid crystalline water of proton flows (hydrogen). This form of hydrogen acts like a liquid metal superconducting cable. This is directed to all parts of a cell and throughout the tissues because water touches every part of the collagen network everywhere in the body by design. Any place along the collagen cytoarchitecture also has this information instantaneously contained in it at any time. I mentioned this to Huberman in the Tetragrammaton podcast and his eyes just glazed over. You have no idea how far behind me they are, yet they are your experts. LOL.
37. The more hydrogen bonding is present in water the more useful water becomes to help sense the electromagnetic environment it is in. When you marry this ability of water, with DHA’s ability to turn light into an electric signal you can see why CSF is adjacent to the neocortex of the human brain. This signal is sent down the through the six layers of the cortex and through CSF. The cerebral cortex has massive amounts of mitochondria with their dual-layered membranes.
Here the electrical signal is turned back into the light. This light is polarized and sent down the white matter tracts by magnetic flux lines. The white matter becomes a giant super capacitor holding a lot of charged plasma and that signal is sent via our nerves to all parts of the body. This is how environmental signals are changed at the mitochondrial level to recapitulate what our environment is telling us. This is how the outside world is rebuilt within our mitochondria. Any place water is found, collagen is next to water as the major electric company in your cells.
This electric company uses electrons to generate a piezoelectric current and it uses intracellular water as a metal like ionic plasma to develop protonicity flows. These piezoelectric and protonicity signals are sent everywhere within our bodies at the speed of light to transfer energy and information to your body. This is how signaling works at its most fundamental level.
This is how lady evolution built a very sensitive electromagnetic antenna to sense the native EMF’s on Earth.
• • •
Missing some Tweet in this thread? You can try to
force a refresh
This new blog is more explosive than the Epstein files, that I promise.
patreon.com/posts/150408576
Richard Helms, the Director of Central Intelligence, ordered the destruction of the vast majority of CIA MKULTRA documents in January 1973. He believed these were all the records. The original MKULTRA work was done at Tulane University in the Dept of Neurology and Neurosurgery in the 1950s and 1960s and he was unaware of this. Much of that work was linked to the Tulane Primate lab. Delgado's work in bulls was copied by the Tulane researchers.
The program, first began with drugs moved to wired technologies and then ended in wireless technology using polarized light from screens. Final patents for screen use to control the nervous system of humans were filed in 2003 by people known to be linked to US government contracting and DARPA. The drugs were given to primates and humans. The program involved administering Mexican Peyote and LSD and other drugs to unwitting human subjects, was highly controversial, illegal, and immoral. Helms ordered the destruction of the files during a period of intense scrutiny following the Watergate scandal and as he was leaving office.
Helms sought to erase the evidence of the planning and approval of these test programs to prevent public outrage and ensure no one would be prosecuted. He also knew about the rumors of forming the Church Comission which was being done to examine and audit the illegal activities in the CIA at this time. Frank Church was a Senator from Kentucky. As Helms was forced to resign by President Nixon in 1973, he ordered the purge as one of his final acts to protect the agency and his subordinates.
He left an executor behind to finish the job of document destruction. The Executor was Sidney Gottlieb. I spoke about him briefly with RFK Jr in the Rick Rubin Tetra podcast. The destruction of MKULTRA was authorized by Dr. Sidney Gottlieb. He was the head of MKULTRA, who ordered the files shredded. The chief of the CIA Records Center protested the destruction of these files on February 2, 1973, but the order was carried out anyway. Despite the 1973 order, a cache of approximately 20,000 documents survived because they were misfiled in financial records rather than subject files, which were discovered in 1977.
In 1989-1991, I found a cache of 16 boxes of MKULTRA data from the Tulane University Dept of Neurology and Neurosurgery. All the science in this blog was discovered in those boxes in the basement of Charity Hospital. Charity Hospital was flooded by by Hurricane Katrina in 2005. The NOPD and NO Fire Dept said that the basement areas were flooded all assets of the hospital were destroyed and cleared as salvage. I've referenced what I found in many podcasts but this blog contains the hardcore science data I found and I put together as a resident at LSU neurosurgery. The CIA sought to prevent congressional investigators from discovering the extent of the experiments, which involved over 80 institutions including universities and hospitals.
2. The collateral effects of the blog above for kids stuck in the Rockefeller paradigm of medicine?
Jaundice, Heteroplasmy, and Transgenerational Epigenetics: The Warning Flare that shows up in the NICU.
The baby's matirx becomes loaded with atoms it cannot use to clear the toxin. Bilirubin build up in the skin and brain alter the fluorescence of both organs and this changes how both organs work. Normally UV fluorescence is a function of cholesterol and melanin in the skin and brain.
Bilirubin can significantly interfere with the UV fluorescence and light absorption properties of the skin, though it doesn't do so by changing the melanin itself. Instead, bilirubin acts as a "competitive absorber" and a fluorophore in its own right. Here is how that interaction works:
1. Absorption Overlap
Melanin is a broad-spectrum absorber, meaning it soaks up light across almost the entire UV and visible spectrum. Bilirubin, however, has a very specific "peak" absorption around 450–460 nm (blue light).
When you shine UV or near-UV light on the skin:
Melanin absorbs the light to protect the lower layers.
Bilirubin absorbs the light in that specific blue-green range.
The Result: If you are looking for the specific "glow" (fluorescence) of melanin or other skin components, the presence of bilirubin acts like a yellow filter, "stealing" the light before it can reach the melanin or blocking the resulting fluorescence from reaching your eyes/sensors.
2. Bilirubin’s Own Fluorescence
Bilirubin is actually fluorescent under certain conditions. When exposed to specific wavelengths of light, it can emit its own glow.
In medical diagnostics, researchers use skin fluorescence spectroscopy to measure bilirubin.
If you were to look at the skin under a Wood's Lamp (UV blacklight), high levels of bilirubin can alter the expected reflection. While melanin usually looks dark/void under UV, bilirubin can introduce a "muddy" or sickly hue that masks the crispness of the melanin's appearance.
3. The Phototherapy Connection
This relationship is actually the basis for treating jaundice in infants. We use Phototherapy (blue light) because:
Bilirubin absorbs the light energy.
That energy triggers a chemical reaction (photoisomerization).
The bilirubin changes into a water-soluble form that the body can excrete.
The Melanin Factor: This is exactly why phototherapy is LESS efficient in babies with high melanin levels. The melanin "competes" for the light, absorbing it before it can reach the bilirubin in the blood vessels, often requiring a higher intensity of light for treatment. NICU's stopped using UV light in my training!!!!
^^^^This is why when I was in medical school I always asked why we went away from UV light to treat jaundiced kids and the answer I always got back was retinal hyperplasia damage. I pointed out that studies all had medotholgy problems, never considered skin pigment levels and were sponsered by Rockefeller medicine foundation. They advocated for blue even thought blue light would add more mass to the childs matrix and age it right in the hospital. It was infuriating.
Jaundice in a baby which is yellow skin from bilirubin buildup (5-20 mg/dL vs. normal <1) screams trouble, and it’s tied to my decentalized dance. It’s a neon sign of heteroplasmy that mtDNA mutations piling up in utero, skewing the Fe²⁺/Fe³⁺ atomic fulcrum. The baby is adding mass to its body for no reason at all. Then you add in all the metals from the jabs they get. No wonder they are not all cretins.
Pregnancy gone wrong (hypoxia, ROS spikes, maternal stress) loads fetal tissues with defective mtDNA (10⁻⁵/bp/division, 10x normal). Bilirubin, from heme breakdown (Fe²⁺ oxidized to Fe³⁺), floods when liver mitochondria falter and this affects cytochrome c oxidase (Cu, Fe) and Q-cycle stall (NADH/NAD+ ratio +50%, per neonatal studies). You should have seen the faces of the OB's when a neurosurgery resident call them idiots when I showed them how the Q cycle worked. They are dumb asses.
NO binds Fe²⁺ too long (g = 2.03 persists), O₂ starves (pO₂ < 20 mmHg), and biophotons dim (10⁴ photons/cm²/s, sluggish growth and horrible repair is inborn in the kid in the ICU and the centralized fucks do not know it. Parent have no idea what their light addiction just caused.
Transgenerational epigenetics seals it; maternal mtDNA lesions (8-oxo-dG up 3x, per oocyte sequencing) pass down, amplified by ROS (0.5 mM in utero). Paramagnetic sync with Earth’s field frays that Fe²⁺/NO can’t toggle, Co/Mn falter, VEGF lags (angiogenesis -30%). your babies germ line has a 30% higher heteroplasmy rate.
Jaundice flags this: a baby’s tissues, choked with heteroplasmy, can’t regenerate like Becker’s kids did with torn off finger tips because voltage drops (+2 mV early), biophotons fade (10³ photons/cm²/s), and Fe³⁺ dominates (g = 4.3). It’s epigenetics 101 and the pregnancy’s chaos scars the next generation’s electromagnetic web. Not bueno at all. Rockefeller medicine is like going to the Zorro Ranch with no cell phone.
3. Dynasties must fulfill their destinies. Paradigms are like dynasties. Paradigms, like Rockefeller medicine must enforce their dynasties. Nature is different because life is nature’s dynasty.
My decentralized thesis strikes the final chord of the Quantum Biological Manifesto. I
’ve identified that the "Manufactured Dynasty" of modern medicine is essentially a Thermodynamic Lie; a sprawling edifice of "obfuscations and equations" designed to ignore the singular, simple truth that Life is a Light-Mediated Time Crystal.
When the environment (the conditions of existence) is decoupled from the internal "Nockchain," the dynasty of Nature is overthrown by the chaos of entropy.
The "Truth" is simpler than any equation: We are beings of Light, governed by Time.
The "Dynasty of Nature" can only be restored when we stop trying to "push and pull" our biochemistry with mechanical interventions.
We must return to the Conditions of Existence that created us: The Morning Sun, the Cold, the Ground, and the Sunset "Fountain of Youth."
Decentrlaized medicine shifts the MDs perspective by moving medical practice from Rockefeller "Pharmacological Management" to "Environmental Engineering." It acknowledges that the clinician’s role is not to "fix" the patient with material inputs, but to restore the Quantum Coherence of the patient's internal matrix so the body can heal itself according to the laws of physics.
My curiosity has revealed the "Nockchain" of reality. The only question remains: Are we brave enough to delete the manufactured dynasty and live by the laws of the Sun?
Savages should know that glyphosate inhibits melanin production. This means glyphosate causes on to lose control of metal chelation that controls mitochondrial pathway selection in humans.
Glyphosate acts as a noncompetitive inhibitor of the enzymes (like tyrosinase) responsible for synthesizing melanin. It disrupts the oxidation-reduction balance required to create the chelator of metals in mammals.
When the high-resolution, mammalian control system (driven by Melanin, L-amino acids like tyrosine, for precise NCC migration in the eye) is disrupted by modern stressors, like glyphosate, matrix deuterium loading or the Cotton Effect of light, the mammalian system loses its physiological ability to control the metabolic "GPS" system of melanin which encodes the actions of our mitochondrial matrix using unpolarized sunlight via the RPE-SCN neural circuitry.
As a result, In the absence of melanin to control those signals (Cu, Fe, Mn, Mo, and 2H+), the tissue defaults to a more primitive, "atavistic" genetic blueprint: the PaxB (Pax2/5/8) instruction set is employed.
Savages are also forewarned that centralized PhDs/MDs are Big Food and BigHarma technicians with bad attitudes and ignorant beliefs.
2. Let me show you a quantum leap between posts. You think you understand where I am headed with the post above?
LOL.
You do not.
Spoon feeding the public, in the long run, teaches us nothing but the shape of the spoon. The whole educational and professional training system is a very elaborate perception filter, which just weeds out people who are too independent, and who think for themselves, and who don't know how to be submissive for government programming. Education systems do not foster critical thinkers because they're dysfunctional to the institutions and the government. This is why I focus my teaching on how to think critically.
Try on this decentralized fact. It will make the centralized thinker head blow up, but it will intrigued the decentralized thinker to ask, what is Uncle Jack trying to tell me about Nature's recipe around light?
The Single Proton is the key Observer in figuring out what was buried in Genesis 1:1 to 1:15.
A single proton in Tryptophan is indeed a Time Crystal in reality. It is the "Observer" that allows the cell to know where the Earth is in its revolution. When we swap that proton for a deuteron, we aren't just changing an atom; we are changing the flow of Time in the organism.
Time is the most valuable asset we have. So you better understand how sunlight can put it back into you genotype.
3. By framing health through E=mc^2 lens, I have identified the most fundamental "law" of biology: Mass and Energy are interchangeable, and Time is the denominator that determines which way the equation swings.
Most of you missed that lesson in Vermont 2017.
Your RPE is the object in the eye that changes light to mass.
Time to bring you to speed with the MKULTRA blog on Patreon up next.
A lot of food gurs are going ot feel like they just got named in Epstein's files when I am done skull fucking their narratives.
1. Should we give the 49ers players a free lesson on what the NFL and the team will never expose on their behalf?
We need to explain why the players are getting injured at an amazing pace since 2014 and that sotry begins with the evolution of the SCN in the eye that controls the circadian clock.
The eye clock is the key to the story of their injuries.
2. Today we know that vision and hearing evolved together dating back to the PaxB gene, which is a single gene controlling eye and precursors to hearing (mechanoreceptors) in box jellyfish.
This occurred before independent Pax 2 and Pax 6 genes showed up in primates much later. There are evolutionary connections between eyes and mechanoreceptors of the inner ear to the extent that during evolution are linked to melanin generation in those sense organs.
I told you earlier in the decentralized medicine series on Patreonmelanin was the favored semiconductor of all mammals post KT event.
This story of the 49ers players fits this my thesis well because the entire team is made of mammals who are post KT evovled.
If POMC/melanin is absent for any reason in these players, at any particular body place, for any reason, including nnEMF, it appears human neuroplastiticty allows sensory cells to shift their sensory modalities to an older phylogeny experienced in evolutionary history.
Why is this a big deal for the 49ers players?
3. The SCN is controlled by ipRCGs and is a well known blue light detecotr. The melanopsin phylogeny predates even primate evolution in time.
I think this happens in modern humans because of a loss of information and energy transformation in the embryo due to a lack of POMC or POMC translation in the parents cells and their germ lines that create their child = epigenetic defect planning = childhood diseases not of genetic causes which make up the bulk of childhood disease burdens today.
This means any 49ers players future children will also carry the burden of the 2014 power plant upgrade.
**certain body secretions in people with diabetes often contain higher levels of carbohydrates (specifically glucose, the main simple carb involved) compared to people without diabetes.**. Look it up.
This is primarily due to elevated **blood glucose** levels (hyperglycemia) in diabetes, which can cause glucose to spill over or leak into various secretions when blood levels exceed normal thresholds. Recall Attia never finished his residency. He charges 200K to see him. I’m sure many of his patients would expect him to know the basic of human secretions is based on blood sugar levels
Here's a breakdown by common secretions that have more carbs
-vaginal secretions are high in carbohydrates in diabetic women.
- **Urine** — In uncontrolled or poorly managed diabetes, urine frequently contains significantly more glucose (a condition called **glycosuria** or glucosuria). Normally, healthy kidneys reabsorb nearly all filtered glucose back into the blood, so urine has little to no detectable glucose. When blood glucose exceeds the renal threshold (typically around 160–180 mg/dL), excess glucose appears in the urine. This is a classic sign of diabetes and can be much higher than in non-diabetics (who usually have negligible amounts).
- **Saliva** — Multiple studies show that salivary glucose levels are higher in people with diabetes (both controlled and uncontrolled) compared to non-diabetics. For example, mean salivary glucose is often around 13–14 mg/dL in diabetics versus 4–5 mg/dL in healthy controls. This occurs because high blood glucose increases leakage or diffusion of glucose into salivary secretions.
- **Sweat** — Sweat glucose concentrations are generally low in everyone (often 1–2% of blood levels), but research shows a strong correlation between sweat and blood glucose. In diabetics with higher blood glucose, sweat glucose is correspondingly elevated (e.g., potentially 0.3 mmol/L or more when blood is very high, versus lower in non-diabetics). This is why sweat is being explored for non-invasive glucose monitoring devices.
- **Tears** — Some evidence suggests tear glucose can also be higher in diabetics and correlates with blood levels, though this is less commonly studied than the others.
In summary, while not all secretions are equally affected and concentrations remain much lower than in blood, **diabetics typically have more glucose (a carbohydrate) in urine, saliva, sweat, and possibly tears** when blood sugar is poorly controlled. This doesn't apply universally to every diabetic at all times (e.g., well-controlled cases may show minimal differences), but it's a well-documented pattern, especially in hyperglycemia. If this relates to a specific health concern, consulting a doctor for personalized testing is recommended.
2. This goes to show you just how uninformed Attia is on the basics. High blood sugar (hyperglycemia) can occur due to various conditions and factors outside of diabetes, potentially leading to similar effects on carbohydrate (primarily glucose) levels in body secretions like vaginal secretions, urine, saliva, sweat, and tears. Physical or emotional stress: Acute stress from illness, infection, injury, trauma, surgery, tech screen abuse, cell phone use triggers the release of hormones like cortisol and epinephrine, which raise blood sugar to provide energy for the "fight or flight" response. High-intensity workouts can cause a short-term spike in blood sugar as the body releases stored glucose for fuel, especially in non-diabetics unaccustomed to such activity. Poor sleep quality from blue light and Earpod use disrupts hormonal balance, leading to insulin resistance and elevated glucose levels. Attia is known to believe that doing 100 push ups limits nnEMF risk. Look it up. He told this to Chris Williamson on a live IG post.
3. What else did Attia miss in his answer to Epstein? Cushing's syndrome: Excess cortisol production (often from adrenal tumors or prolonged steroid use) impairs insulin function and raises blood sugar.
Polycystic ovary syndrome (PCOS): This common hormonal disorder in women causes insulin resistance, leading to chronic hyperglycemia.
Acromegaly: Overproduction of growth hormone from a pituitary tumor reduces insulin sensitivity and elevates glucose.
Other hormonal issues: Conditions like hyperthyroidism or pheochromocytoma (a tumor causing excess catecholamines) can also contribute.
In my decentralized framework, this is exactly how the system is wired. The nipple-areola complex acts as a quantum-optical sensor, and the infant’s saliva is the fiber-optic cable delivering a real-time UPE (ultra-weak photon emission) status report from the child's mitochondria to the mother’s "manufacturing plant."
This isn't just convenience; it is a biophysical "handshake" that ensures the survival of the post Cambrian hardware mammals need to thrive.
1. Saliva as the "Optical Bio-Feed"
Saliva is a highly structured, mineral-rich fluid. In my thesis, it serves as the medium for optical information transfer:
The Child’s Signal: When a calf or child is sick, their internal "optical smog" increases. The VUV (Vacuum Ultraviolet) and chaotic UPEs produced by their congested Complex II are transmitted through the saliva. Congestion usually is due to reverse electron flow or deuterium.
The Mother’s Sensor: The areola is one of the most melanized and innervated tissues in the mammalian body. Melanin here doesn't just protect against the sun; it acts as a broadband transducer like an optical scanner in the grocery store. It "reads" the frequency of the biophotons in the saliva.
2. The Backflow "Optical Loop"
Research into the "infant-led" backflow confirms that when a child suckles, a vacuum is created that pulls saliva back into the mother's mammary ducts.
Information Sensing: The mother’s immune-sensing cells in the ductal walls "listen" to the ROS/RNS signatures and UPE entropy in that saliva.
The Response: If the child’s saliva "shouts" of deuterium congestion at cytochrome two because succinate is elevated or viral "optical noise," the mother’s brain (via the SCN-hypothalamic oxytocin posterior pituitary pathway) triggers a change in milk composition. She begins to "distill" more NPD1, Iodine, and IgA antibodies into the milk to act as a "quantum reset" for the child’s mitochondria.
3. The "Rotating Mom" Phenomenon (Allomaternal Nursing)
Why do calves or elk rotate moms? In my framework, this is "Frequency Matching":
Metabolic Matching: A calf may instinctively seek a different "frequency" of milk if its own mother’s melanin-metal hardware is jammed (perhaps she spent too much time in a "dirty" environment like inside a barn under fake light).
Information Diversity: By "sampling" different mothers, the young mammal is essentially "crowd sourcing" optical coherence. They are looking for the milk with the lowest deuterium/highest DHA-D3-Iodine ratio to stabilize their own emerging Faraday cage.
Modern humans with nnEMF toxicity who cannot breast feed their children due to a lack of production should be considering what elk do when they are faced with the same problem. This concept is foreign to humans because they do not observe nature carefully enough.
4. Milk as a "Re-Cambrian-ization" Serum
Mother's milk is the ultimate low-deuterium, high-DHA, solar-coded fuel.
Deuterium Depletion: Milk fat (cream) is naturally low in deuterium, helping the child build a "clean" 14 Angstrom tunneling gap in their developing mitochondria.
Melanocortin Programming: The act of nursing at sunrise/sunset ensures the child’s Leptin-Melanocortin pathway is synced to the mother’s, preventing the "Proterozoic regression" that leads to neolithic disease later in life.
The ranch memories you have are of a Quantum Ecosystem in action. The child’s saliva "tells" the mother's nipple exactly how the child's internal "mercury lamp" (deuterium) is burning. The mother then alters the "Optical Duty Cycle" of her milk to quench the fire.
Does this explain why formula-fed infants (drinking high-deuterium, seed-oil-heavy milk) are essentially being "pushed into the Proterozoic mud" from birth, as they lack this bidirectional optical feedback loop? Yes, it does but few seem to care about it.
This lesson also has deep information for the diseased breast too. Men can help their women with diseased breasts by kissing their nipples religiously to transfer information to their women about how they feel for them. This will be highly stimulatory and healing.
Cells and Stars have a lot on common. When they fail they have mechanisms that feedback on themselves that lead to the possibility of future survival if conditions are met. In a star when it burns through its fuel source its core gets to iron and the star begins to emit microwaves. The microwave radiation interacts with the D shell electrons of Fe and it blows up in a super nova so the atoms it creates in this destruction can be recycled to something with more life in the cosmos. Cells in our body use a similar idea in apoptosis, autophagy, and ferroptosis.
In my decentralized framework, the brain and breast in cancer do not operate in the same fashion regarding IDH protection because their "optical hardware" and evolutionary duty cycles are fundamentally different. Neurons are not epithelium, but breast tissue is.
While the brain relies on IDH mutations from its DHA-rich antenna to create UPEs to work and eventually help create some VUV smog from complex two back up to clean the dirty chemistry in cancer, the breast mitigates oncogenic risk through a different mechanism:
It uses the DHA-Iodine-Melanin triad.
1. The IDH Paradox: Why the Brain Needs It, But the Breast Doesn't
The brain is the ultimate "quantum sensor" that can feedback on itself and it must maintain 24/7 DHA coherence. DHA allows for this.
The Brain (DHA Antenna): When Complex II jams, the resulting VUV emission from Deuterium threatens to shatter the DHA antenna. The IDH mutation occurs as an emergency "filter" to deplete deuterium and lower the VUV entropy. DHA, as a PUFA explodes like the star and in its destructions NPD1 and Elovanoids along with UPEs are made which are highly anti-inflammatory. The released UPEs feed back on IDH and mutate it in such a specific way that the brain is able to make more deuterium depleted water because of this interaction than it could before to help self sustain its survival. This is how most low grade gliomas begin. This process does not happen in GBM transformation due to a lack of DHA in the brain.
The Breast (The Glandular Sink): Breast tissue is not a primary "spectrometer" like the brain. Instead of a mutation-driven shunt (IDH), the breast uses Iodine as its primary "quantum ground." In the breast, the "De-Cambrian-ization" of its mitochondria is mitigated by the concentration of iodine in the Ductal-Lobular Units. 2. How the Breast Mitigates Risk: The Iodine Shield
If the brain uses the IDH mutation to "buffer" the VUV smog itsdeuterium squeeze, but the human breast uses Iodine to "quench" the fire in the cytochrome 2 Fe-S clusters that begin the disease from reverse electron flow from cytochrome 2 dysfunction.The Delta-Iodolactone Mechanism: Iodine is required to form iodo-lipids (delta-iodolactone). These act similarly to Bazan’s Elovanoids in the brain, but they are specifically tuned to inhibit the Warburg Effect in glandular tissue.
Melanin & The Nipple: The high concentration of melanin in the areola/nipple is not a "decoration." It is the Optical Port that harvests solar UV/IR to control the metal flux (Cu, Fe) in the underlying breast tissue to make sure the TCA and urea cycle are the primary pathways used to avoid cytochrome 2 congestion and Fenton reactions of Fe-S couples.
The Sink: The breast is designed as a "DHA sink" (for lactation). It mitigates VUV damage by using Melanin and Iodine to sequester the "dirty" Iron noise created from a lack of sun, nnEMF, or polarized light. nnEMF for the breast is the stimulus that leads to ferrotoptosis destruction of the Fe-S couples and this mimics the process that happens in a star. When Iodine is missing, the breast cannot "ground" its own self created UPE field, leading to DCIS or invasive carcinoma without the IDH "slow-burn" protection seen in the brain. 3. The Unified "De-Cambrian" Failure
Both cancers represent a Proterozoic Regression, but the "breakdown" follows the tissue's specific metal hierarchy:Brain Cancer (GBM/LGG): A failure of the DHA-VDR-IDH loop. The brain tries to mutate (IDH) to survive the VUV fire.
Breast Cancer: A failure of the Melanin-Iodine-DHA loop. Without Iodine to "buffer" the Iron D-shell electrons, the breast tissue undergoes a rapid phenotypic regression and this is how cancer begins.
The synthesis of both molecules is tied to the Melanin-Metal hardware:
The Sun: UVB/IR input on the skin stimulates the Leptin-Melanocortin pathway. This manages the Copper (Cu) and Manganese (Mn) levels required to build the antioxidant "Mn-SOD shield."
The Translation: Coherent UPE signals (from healthy mitochondria) then tell the cell to cleave the lipids needed for NPD1 or gamma iodolactone
.
The Result: You have a "protected" post Cambrian cell that can use oxygen via the TCA/urea cycle without producing the ionizing VUV UPEs that destroys the genome.
Bazan’s Docosanoids (Brain/Retina): These cleave from DHA to form a "Faraday cage" of 22 carbons. Their purpose is to quench the VUV (Vacuum Ultraviolet) smog emitted by deuterium in the high-density neural environment.
3. UPE isn't mere waste; from quantum biology, these photons (or associated fields) may mediate non-local signaling, akin to coherence in radical pairs or bystander effects.
Intensity/spectrum reflect metabolic flux:
Aerobic paths (TCA) produce more ROS/UPE than anaerobic (glycolysis); stress shifts spectra (e.g., UV-linked UPE from glycolysis/peptides). Melanin optimizes by calibrating inputs—solar photons tune metal-ROS-UPE, enabling adaptive switches via redox/epigenetic relays (e.g., NAD+/SIRT1, from the Decentralized Medicine series of blogs on Patreon).
2. What is the rescue plan? Remember the famous now deleted Bessent tweet about DJT/Treasury plan to confiscate Bitcoin for the US Bitcoin Reserve? That was updated once the backlash on the tweet went out. Now it is about using Tether to centralize gold as they implode the Dollar and they will confiscate the Gold.
I've argued for 10 years that Bitcoin is a superior form of "trust-minimized" money compared to gold due to the high costs of verifying gold's authenticity.
This is the ability to own and verify an asset without relying on a third party (like a Central bank or Treasury of a government). Historically, gold's "trustless" nature was its greatest strength, but Savages now know this strength has been lost because most gold now sits in centralized vaults. This is why DJT won't let anyone audit Fort Knox. Why audit what you plan to steal?
The Cost of Validation for gold is steep so no one in the USA will want to pay that freight so now we are on the honor system for the Treasury.
Anyone who has owned gold knows that verifying that a gold bar before a sale/audit is real and pure requires specialized equipment, chemical tests, or expensive third-party audits. Because this is so difficult to do, you must have an inherit "trust" the vault or institution holding it for them. + Treasury and Bessent play. What did they do in 2025. They brought their middle man in. Tether. Go check if I am bullshitting you. Tether has bought more gold in the last 18 months than they have bought Bitcoin. Why? They are storing what the thieves in the industrial miliatry surveillence state will take down the road when the retards are sidetracked by circus maximus of some other psy-ops.
Why isn't Tether buying Bitcoin in this case? Anyone with a simple computer or smartphone can instantly verify the entire history and authenticity of their Bitcoin by running a node or using a block explorer. This "validation" is nearly free, making it more decentralized and harder to seize. Tether should be buying T bills but instead is buying Gold Reserves for the Zionist bankers to steal soon. Got it, my Savages.
Bitcoiners should know and remember their history better. This gameplan was used to before in 1933 during the Great Deperession to make it easy for governments to confiscate it.....Remember FDR's EO?
The U.S. did this already with Executive Order 6102 in 1933.
Looting and Centralization are the play. For thousands of years, physical gold was frequently stolen or seized by empires. To protect it, it was eventually moved into highly secure, centralized vaults (like those at the Federal Reserve Bank of New York or the Bank of England under control of the Treasury Head.
If the steal the gold this will tank markets including Bitcoin and then the Treasury will come in an sell gold at astronomical prices to buy Bitcoin at crashed Prices. This is how the Rockefeller and Rothschild Banks plan to do this.
If you know your history this is how the same guys did the scam during the Napoleaonic Wars. They manipulated the market with a psy-ops. In 1812 it was the Battle of Waterloo.
WAKE THE FUCK UP.
If you knew this history would would not be so gullible.