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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Sep 10
The retina thins from the effect of man-made light and a lack of sunlight, and then your risk of Frontotemporal dementia rises. The OCT test is the best screening test for FTD. We have familial and mtDNA FTD.

The retina acts as a ‘window to the brain," and that window changes the photolithography of the retinal cells. When the light is not optimal, the retina thins and the brain degenerates. Retinal degeneration has been detectable in mutation carriers prior to the onset of cognitive symptoms, establishing retinal thinning as one of the earliest observable signs of familial (frontotemporal dementia).

nnEMF and a lack of sun lead to neural degeneration, which is primarily driven by the abnormal accumulation of misfolded proteins within neurons. Light controls the confirmation bending of proteins. The DNA code controls the AA sequence and secondary bending, but quantum processing determines tertiary and quaternary bending by UPE transformation in cells. The most common protein abnormality in FTD is the tau protein, also known as TDP-43. These protein aggregates damage and kill nerve cells, leading to brain atrophy (shrinkage) and the resulting behavioral, personality, language, and movement problems characteristic of FTD. I believe this protein also thins the retina. Light is the offender.

Blue light increases RBC turnover in the retina and changes the oxidation state of iron, and this affects the synthesis of new heme proteins in the retina and brain. Oxidative stress is a key trigger in this disease because it increases peroxide production (ROS), which alters the UPE signature of cells in the construction of the heme proteins, which changes the photolithography inside the retina and brain. Changing the photolithography = altered protein folding via the Golgi apparatus and RER. TDP-43 is a biomarker of redox imbalance in FTD-related UPEs.

The path of energy in life, based on the evidence we have as a species now, is that Optical photonics began 13.8 billion years ago. The photoelectric effect was born from the rudimentary physics present in the early universe. Photonics precedes all chemistry of all types. Functional medicine does not realize this or teach it. Molecules were and are innovated by redox chemistry, and each one has an electromagnetic barcode to program its possible states around the star it evolved in.

The TDP-43 molecule is codified by light in its absorption and emission spectra. This links it to aberrant UPE production in the central retinal pathways, as blue light increases heme turnover to alter its biophotonic signal. Look at all the places a UPE can be made from in a cell to cause this disease on the slide. You'll also see that light carries spin information that can create this disease.

Where there is a change in matter (TDP-43), there must also be a change in atomic molecular geometry in that tissue. Where normal cellular geometry ceases to exist, we will find light as the key agent of change. When both exist in simultaneity, you'd better understand Fermat's law and the photoelectric effect to understand what a disease really is. Right now, in centralized ophthalmology, none of them do. See Bruce Willis.

THE BIOPHYSICAL CODA of FTD: When Turing realized morphology in all living things had a photonic timeline in Nature, he wrote a key paper on morphogenesis. Light signaling predates biochemistry and molecular creation from redox chemistry. This paper suggested that a system of chemical substances, called morphogens, could react together as a symphony does and subsequently diffuse their electromagnetic, electrochemical, and photobiolelectric information through a tissue to sculpt it, changing its morphology without using the nuclear genome.

Turing stated in 1951 that this set of circumstances is adequate to account for the main phenomena of morphogenesis. In such a dissipative system, although the cells may originally be quite homogeneous at the embryo stage, this information upload may later develop a pattern or structure in the embryo due to the instability of the homogeneous equilibrium caused by light pollution in the parents' germ line, which is triggered by random disturbances in the tissue. Those random disturbances are UPEs. The random disturbance he hypothesized about turned out not to be random at all. UPEs are created in cells by light AMO interactions via redox chemistry that directs their own sculpting from the nuclear genome. The UPE energy transformation is driven by the mitochondrial genome, which is subject to light in the environment to create UPEs and eventually by reactive chemicals like ROS/RNS inside all cells. Any disease linked to aberrant UPEs will always present as having a spectrum of maladies. FTD has that optical signature. ncbi.nlm.nih.gov/books/NBK55928…Image
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2. The GLP-1 Drug Connection: Weight Loss at a Cost to Your Eyes and Ears

GLP-1 drugs like semaglutide (Ozempic, Wegovy) and liraglutide (Victoza) are prescribed for type 2 diabetes and weight loss, helping millions shed pounds by curbing hunger and stabilizing blood sugar. However, literature suggests that they can affect the eyes and even the inner ear (cochlea), which ties into the light biology disruptions we just discussed.

Effects on the Eyes

These drugs cause rapid weight loss, which triggers fluid shifts and reduced blood volume in the body.📷This can stress the delicate blood vessels in your retina, leading to:
Worsening diabetic retinopathy: In people with diabetes, GLP-1s can make existing eye damage worse, causing blurred vision or macular issues.

Increased risk of vision loss diseases: Studies link them to a doubled risk of neovascular age-related macular degeneration (nAMD), a leading cause of blindness.

There's also a higher chance of non-arteritic anterior ischemic optic neuropathy (NAION), where blood flow to the optic nerve drops, potentially causing sudden vision loss.

Blurred vision and other issues: Common side effects include visual impairment, which can start as early as 10 days after use. While not everyone experiences this (risks are low but real), regular eye exams are recommended for users.

How does this relate to light biology? The fluid shifts and oxidative stress from GLP-1s can amplify ROS production, disrupting UPEs and protein folding in the retina, much like exposure to bad light. This thins the retina, mimicking the early FTD signs, and could raise dementia risk indirectly through disrupted circadian rhythms.

Interestingly, while some research suggests GLP-1s might protect against general dementia by reducing inflammation, their eye effects could counteract that, especially in FTD-prone folks. My TED talk was banned because BigHarma was afraid I was going to obliterate their GLP 1 train by showing the world why they banned stopped the leptin trials early on weight loss.Image
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3. Since the ear also processes sensory info tied to your body's clock, this could feed into broader brain degeneration.

Effects on the Ears (Cochlea)The cochlea, your inner ear's hearing hub, isn't immune. GLP-1s are linked to hearing problems like hearing loss, vertigo, tinnitus (ringing), and eustachian tube dysfunction (feeling of ear fullness).

Rapid weight loss can disrupt fluid balance in the ear, similar to the eyes. Diabetes itself raises hearing loss risk via blood vessel damage, and some GLP-1s (like exendin-4 types) heighten it further. The GLP target in the ear is the stria vascularis.Image
Read 4 tweets
Sep 7
I tried to pull the veil back on the layers of the Deep State and where they are linked and why they are linked. It is a nasty story of deceit and ideological fascism where science was stolen to control modern humans with Light, drugs, and jabs.

The historical links you must know.  Why is Israel so misunderstood? Propaganda is its shield, so you can never know who is really behind it.

It is British Imperialism dressed in drag to protect its ideology of fascism, which is what a Fabian really is.

The billionaires of today are not the architects of Zionism
They’re the actors. Elon. Thiel. Gates.
They run infrastructure, but they don’t own the world.
They were groomed by systems older than corporations.
The real owners?
• BlackRock, Vanguard, BIS — own the assets
• Rockefeller, Rothschild, DuPont — own the timeline
• WEF, CFR, Chatham House, Fabians — write the script
• Think tanks + foundations — enforce ideology
Occult orders + Straussian elites — justify it all as “destiny”
This is not capitalism.
This is a technocratic theocracy—where power is hidden in algorithms, law, debt, and narrative.
They don’t fear elections.
They fear recognition.
They fear you finding out what their plan really is.
Why must we decentralize medicine?
Because it eliminates centralized Rockefeller Medicine from the World.
That is a world where drugs and jabs are used as weapons of control.
Time to wake up and do your diagnosing better today than you did in the past.

x.com/JuanGutiCA714/…
2. True Evil with assorted atrocities most often occurs when the most respectable and intelligent of people fall for it. The wise never do. They sniff out and diagnose the problem of centralization to avoid collateral damage. Be careful who packs your parachutes. Image
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3. What is modern gaslighting of the jab injured really? It is cloaked in pardons and Nobel Prizes given to the architects of the crimes. Image
Read 4 tweets
Sep 4
I started a huge Barista FIRE on the boat it appears with my Bitcoin talks with him every AM. He apparently was quite influential with the young staff and told them all they were working communist hours for communist pay, and when his manager heard it spill over to our morning conversations and how many of the krewe I am Orange pilling, they axed him. He was escorted off the book quickly in Peru, and I never knew it until this AM. Some of his barista folks confirmed it got hot quickly.

What Is the FIRE Movement, and Where Does Barista FIRE Fit In?

FIRE stands for “financial independence, retire early.” The FIRE movement puts forth the idea that becoming work-optional isn’t about reaching a certain retirement age; it’s about having enough money invested that the compound interest gains can sufficiently cover your annual expenses. Bitcoin really changes the mix for young people locked into communist like employee environments.

This is achieved by reaching what is called your FIRE number. A (very) rough calculation of FIRE number is to multiply expected annual expenses when no longer working by 25. This is the amount of retirement savings you’ll want to have ready to tap, but know that performance on investment accounts can vary widely from year to year. A traditional FIRE number is typically well north of $1 million.

There are many people who don’t actually want to stop working and enter full retirement. Instead, they want to downshift to doing more fulfilling work, or they want to be able to work part-time so that they can spend more time pursuing hobbies or passions. In jobs like medicine and cruiseship workers the math works rapidly but for different reasons. So when I explained this to Christopher he seemed to catch fire like I had poured diesel fuel on him. Never thought he'd get canned for it that fast. I guess capitalism is a bad antidote for the communist boat life.Image
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2. The Origins of the FIRE Movement

In 1998, three researchers at Trinity University published the results of a study on retirement savings.

Their projections found that, if an investor had a certain multiple of their income saved up and withdrew 4% or less of their nest egg each year, their chances of depleting their savings in a 30-year period were zero. I re-did this calculation in 2013 and added Bitcoin CAGR to the mix, and the results were more stunning. That is when I realized I could bail on centralized medicine and began teaching this method to my MD clients. Sadly, most of them crumbled because they could not fathom walking away from their jobs because of their programming. The Trinity research group was based on rates of return since the invention of the 401(k) and other tax-advantaged retirement accounts, and later became known as the "Trinity study."Image
3. The results of the Trinity study were first published in the American Association of Individual Investors Journal in 1998.

This research led to my reframe: If you could grow your nest egg large enough that the interest alone covered annual expenses and other medical expenses, most or even all of your principal would be protecting, preserving your wealth. I tweaked this big time. I realized that the decentralized mitochondrial life could bring medical expenses to zero and then I could power up my savings with the Bitcoin CAGR i could make money grow on trees for decades. IT was how I figured out that the one thing killing me, my job, could be eliminated rapidly. I got a huge settlement from a cruise incident related to a paleo meathead, and I yolo'd it into the program, and within a year, I found out this was going to be life-changing.

The Centralized Fiat Retarded Say Money Doesn’t Grow on Trees......but decentralized geniuses know it happens.

If your tree is a large enough nest egg due to the Bitcoin CAGR, it actually does. I began to realize that the traditional retirement age wasn’t dictated by age, but by whether you reach financial independence. Thus, the ORANGE FIRED MD lifestyle was born.

FIRE stands for Financial Independence, Retire Early. Over the years, however, many ORANGE FIRED MDs Savages began to break from core FIRE principles and define FIRE variations that better suit their lifestyle goals. I helped many of my tribe do just that. Membership matters in this tribe.Image
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Read 21 tweets
Aug 26
1. ANSWER: In ALAN contexts, blue light suppresses melatonin, which normally inhibits AVP and cortisol, leading to unchecked vasopressin release during "light stress." This causes a reactive hyponatremia in the posterior pituitary, activating brain osmoreceptors and RAAS, raising blood pressure and stress hormones, which fragment sleep and impair daytime recovery. They also chronically degrade the mitochondria in these neural tracts.Image
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2. Now for the dirty details.
Precise Mechanisms of Sodium Regulation in the Brain and Circulatory SystemSodium (Na+) homeostasis is tightly regulated to maintain osmotic balance, blood pressure, and neuronal function, with disruptions like hyponatremia (serum Na+ <135 mEq/L) directly impacting sleep via arousal, cognitive fog, and fragmented rest. The brain acts as the central sensor and regulator, while the circulatory system executes adjustments through hormonal and renal pathways.

Brain's Role in Sodium Sensing and Control: The hypothalamus, particularly osmoreceptor neurons in the supraoptic and paraventricular nuclei, continuously monitors plasma osmolality and Na+ levels via stretch-sensitive ion channels. When hyponatremia occurs (e.g., from ALAN-induced vasopressin overrelease diluting blood Na+), these neurons trigger arginine vasopressin (AVP, or antidiuretic hormone) secretion from the posterior pituitary.

AVP promotes renal water reabsorption via aquaporin-2 channels in the collecting ducts, conserving water but exacerbating dilutional hyponatremia if unchecked. In the brain, low Na+ also activates the subfornical organ and organum vasculosum of the lamina terminalis (circumventricular organs lacking a blood-brain barrier), which integrate signals from baroreceptors and chemoreceptors to modulate thirst and salt appetite. Chronic hyponatremia impairs neuronal excitability, leading to symptoms like headaches and insomnia, as it alters membrane potentials and synaptic transmission.

Circulatory System Integration with Hormones: In the periphery, low Na+ (hyponatremia) is sensed by renal juxtaglomerular cells, triggering renin release, initiating RAAS: renin converts angiotensinogen to angiotensin I, then II, which stimulates aldosterone from the adrenal cortex to enhance Na+ reabsorption in the distal nephron and potassium excretion. This raises blood pressure to restore volume but can cause nocturnal hypertension, disrupting sleep architecture (e.g., reduced REM). Cortisol, released from the adrenal cortex in response to stress signals (including ALAN and hyponatremia), amplifies this by promoting Na+ retention via mineralocorticoid receptors and enhancing sympathetic activity, increasing heart rate and arousal. Vasopressin interacts with cortisol and RAAS; for instance, AVP potentiates cortisol's effects on water balance, while cortisol feedback inhibits AVP in healthy states, but ALAN disrupts this, leading to unchecked stress responses. Atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) counterbalance by promoting natriuresis (Na+ excretion) when blood volume rises, but in hyponatremia from SIAD (syndrome of inappropriate antidiuresis), this balance fails, perpetuating low Na+ and sleep disturbances like frequent awakenings.
3. So Emily, what you should do is see the AM sunrise every AM. Drink DDW water and add high-quality salt to the water, and within 2-4 weeks, you will sleep much better. These slides support the tweets, and the last one with the D20 water spectrum really hits the mark. Image
Read 5 tweets
Aug 21
A couple of points: Not all human cells have mtDNA. See adult blood cells. This is a big deal when you consider their absorption spectra. 200-600 nm light with a sharp cut-off. Also, blood still transforms energy into UPEs. And since blood fills 20% of our CO to the CNS, this also has implications. The retina and gut increase their blood flow with light use and feeding. Feeding is a light-based phenomenon since all food webs link back to photosynthesis.

In humans, light stress does not force mitochondria to react exactly the same way as infection (no ATF4 surge, different folate handling), but there are partial overlaps in ISR activation, 1C remodeling, and mtDNA signaling.
This suggests UV light acts more as an external folate depleter for DNA protection/photorepair, while infection is an internal ATF4-orchestrated defense. If environments lack natural light controls (as in modern human life), it should exacerbate mismatches in folate biology. For deeper dives, I'd recommend reviewing the ATF4-UV papers for experimental details.

Folate as a Light-Responsive Switch: My patreon has made this point over and over again, natural folate (not folic acid) is photosensitive, degraded by UVB, and shows seasonal lows in summer (higher at low latitudes, with gender differences showing men have lower levels). This would act as a "switch" for mitochondrial/genome control, linking to melatonin/tryptophan pathways and neurotransmitter synthesis (e.g., serotonin, dopamine). In low-light/artificial blue light environments (e.g., indoors), folate stability increases unnaturally, disrupting methylation/DNA synthesis and contributing to diseases like Alzheimer's, Parkinson's, or diabetes (via melanin quenching loss and superoxide buildup). People with MTHFR and COMT defects are supersensitive to ALAN and a LACK OF SUNLIGHT. This is echoed all throughout my decentralized photo-bioelectric thesis: light refines folate via photosynthesis/food webs, but artificial setups bypass this, leading to transgenerational effects.

No Seasonal/Light Controls: absent natural light cycles (e.g., constant artificial light), retinal/CNS signaling should be expected to dysregulate—e.g., excess folic acid fortification (since 1996 in North America), which overloads 1C pathways, causing cognitive haze, sleep issues, or neural migration problems in lit environments. This photonic effect is completely missed in centralized medicine and is really missed in functional medicine, which pushes for excessive folate use with SNPs. These people need more sun and less ALAN, not drugs.

Black Swan Mitochondriac View: Melanin (from UV-absorbing aromatic amino acids) quenches mitochondrial superoxide, protecting against neurodegeneration. Blue light destroys melanin and heme proteins, amplifying risks from ALAN and a lack of sunlight which aligns perfectly with UV's mitochondrial stress but without the adaptive folate restriction seen in infection.

Now the picture is full. patreon.com/posts/decentra…
2. Why is this tweet important to the jabbed? If you follow the work of @Kevin_McKernan you'll find in his blogs many mentions of pseudouracil and jab injuries. Then you look at my blogs on jab repair, and you'll notice I recommend Tropical relocation as the best risk reduction for the compliant. WHY?

Did you know that in humans, UVR depletes folate in skin and blood, inducing S-phase arrest, affecting uracil misincorporation (frame-shift mutations), and sensitizing apoptosis in keratinocytes. This isn't "damage" but a permissive environment for seasonal phenotypic changes, e.g., increased melanin production to protect folate stores. When you understand the photorepair mechanism, you will see this is how humans can block the DoD and BigHarma death mechanism from uracil replacement induced by the jabs. @MdBreathe None of the COVID experts have this sophistication. They are still pushing detox answers when it is crystal clear that redox biology is the path for the Savage trying to stay alive and away from disease.Image
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3. Individuals with MTHFR C677T (thermolabile variant) are indeed supersensitive to light/folate fluctuations, as the mutation impairs folic acid conversion to 5-MTHF. High folic acid may select for this allele evolutionarily, acting as a "genetic time bomb" by promoting unmetabolized buildup and altering DNA/RNA biology.

People who have this SNP and took the jab have no choice but to move. If they do not, they will be taken out to Taper the Ponzi. This variant requires higher folate for stability, making carriers vulnerable in low-UVR (winter/indoor) settings, where blue light further degrades melanin (a superoxide quencher), exacerbating mitochondrial stress.Image
Read 5 tweets
Aug 19
If Einstein was correct that energy = mass times the speed of light squared (E = MC2), then how did biology make all life from that simple equation? As I looked up, the sun hit me in my eyes. I realized the link, right there. I had to reverse Einstein’s equation to see how life made sense of the chaos on our planet, to create life from it. E = MC2 is a simple math equation using simple variables we all know.
Truth Bomb #2: Life is energy and energy is life according to this equation.
It also implies that the equation can also be reversed mathematically. The “Commutative Laws” say you can swap numbers over and still get the same answer. A + B = B + A. Biologic sciences have pretty much ignored E = MC^2 for much of the last 108 years since its discovery. It has been felt to be the domain of subatomic physics and of theoretical physics, and astronomy. Physicists and chemists have always read Einstein’s masterpiece equation from left to right. This helped them explain the massive power generated from the nuclear fission of atomic blasts. As a surgeon, I realized there is were no nuclear explosions occurring in cells to generate energy. I reasoned, biology could not use the reaction that way, so life had to find another way to do it. I thought, that maybe, life at its origin on the chaotic Earth, sought order from the environments it had to endure to survive. If that was correct, then all biology must start with the speed of light, squared and not with energy. I felt I had to reverse Einstein’s equation in my head to figure the riddle out. It made sense because today we know all life makes energy from the sun or from electrons in our mitochondria. Plantlife uses the photons or electrons of the sun to make its energy efficiently. Animals use electrons to make fuel in the mitochondria in the form of ATP.
The M, the ‘mass’ part of the equation brings in the elements of space/time and gravity from physics. This is a topic biology rarely deals in. This is where the riddle got complex for me. This implies the way the mitochondria account for energy has to include a very precise timing procedure as a part of energy generation. I knew from mitochondrial biology that is precisely what the “Rolex” in our head does at the SCN by responding to the magnetic field of the Schumann resonance of the Earth.
But there is more.
Food is information of light from the sun. It is also energy. This means that info and energy are linked. It turns out they are linked via the concept of mass.
Shannon took the vague concepts of information and pinned them down to what its essence was all about.
He asked what was the minimum requirement needed to create a message that could still be deciphered well.
The equation he came up with looks identical to Boltzmann's equation for entropy. This means Information truly links to thermodynamics.
Boltzman gave us the statistical explanation of the second law of thermodynamics. In 1877 he provided the current definition of entropy,
In 1948 Shannon figured this out by mathematically learning how to measure the information in the messages
Shannon realized that the quantity of the message had ZERO to do with its true meaning.
Physicist John Wheeler extended Shannon's ideas further.
Wheeler tells us every particle in the universe emanates from the information locked inside it.
My idea at my KLC clinic: This idea has massive implications for mitochondrion who deal exclusively with light, electrons, and protons in cells.
Wheeler’s ideas have been expanded recently by Vopson (dark energy non-believer)
His paper says that not only is information the essential unit of the universe but also that it is energy and it has to have mass.
To support this claim, he unifies and coordinates special relativity (1905) with the Landauer Principle (1961)
Landauer predicted that erasing even one bit of information would release a tiny amount of heat, a figure which he calculated = mtDNA is a heat engine
If information is energy, Information, once created has to "finite and quantifiable mass."
This connects information directly to energy. E-mc^2
When information is lost in the system there has to be a change in mass in the system..............
These ideas fueled the EMF 2 blog post at jackkruse.comImage
2. It amazes me how ignorant the paradigm is about AM sunlight. AM sunlight is filled with high intensty red light and a smaller amount of blue light. This is why the color temperature of AM sunlight at sunrise is around 1600K and it is 16,000 K at sunset. High intensity red light in the AM is the light that Nature uses to stimulate testosterone release in men. UV light is a potent "off switch" for testosterone action in the blood. It amazes me that this PEER reviewed article has no clue that AM SUNLIGHT is the circadian controller of testerone level in MEN.

They want to use fake light.........to do the job of the sun.
Ridiculous.

The use of light therapy dates back to ancient civilizations, going as far back as the ancient Egyptians and Indians, who used sun- light (heliotherapy) for healing and promoting health. The therapeutic use of light energy was more fully appreciated in the late 19th century when a Danish physician-scientist, Niels Ryberg Finsen, demonstrated the benefits of red and blue light in the treatment of lupus vulgaris and was recognized with the 1903 Nobel Prize in Medicine and Physiology. In 1960, the L.A.S.E.R. (Light Amplification by Stimulated Emission of Radiation) by Theodore Maiman was invented, based on theoretical work by Albert Einstein in 1917.

This brought renewed attention to the therapeutic light energy field. The monochromatic, coherent, and collimated nature of lasers led to immediate interest in their biologic effects. In 1967, Endre Mester, a Hungarian physician-scientist, reported that low-dose laser treatments were capable of promoting wound healing and hair regrowth in mice. He termed this phenomenon photostimulation and went on to demonstrate the efficacy of this treatment in human patients with skin ulcers. medicalnewstoday.com/articles/31296…
3. When a human lives in a poor environment loaded with Blue light and nnEMF it stimulates a type of cell death called 'ferroptosis'. Do you know about it? Most gurus have never even herd of it. This is why you must be careful who you allow to pack your parachute.
Ferroptosis is defined by the iron-dependent accumulation of lipid peroxides when heme containing photoreceptors undergo damage. Most people have no idea that this occurs in the blood (catalase), mitochondrial cytochromes, and th eP450 system. All of them containing heme (iron based) proteins that work with light. Ferroptosis is associated with the abnormalities I look for in peripheral blood smears at Kruse Longevity Center and it is genetically (DNA/mtDNA) and biochemically distinct from other forms of programmed cell death such as apoptosis, necrosis, and autophagy. It is linked to why many gas anesthetics are linked to neurotoxicity in people with neurodegeneration. It also is linked with people who are floxxed and have many other mitochondrial redox linked diseases.
It appears this new mechanism is driven by downstream inactivation of glutathione peroxidase 4 (GPX4, Yang et al., 2014). Peroxidase enzymes are ALSO ALL HEME containing proteins. I believe the fluoride in the inhalational or prescription drugs is ONE of the proximal cause of the iron-dependent accumulation of lipid peroxides because it causes a dielectric collapse in the metabolic water around these proteins in mitochondria. I also think this leads to melanopsin dysfunction in the circulatory system where the most heme iron-containing proteins exist in man. The tell tale sign is when retinol levels in the plasma rise sharply because the Vitamin A derivative is running free destoying photoreceptors as it goes.
The second critical spot they are found is in the mitochondrial membranes of man. This has not been studied as far as I can tell in 2019. The normal dielectric constant of water is 78 in bulk water but it has been shown to be 160 in metabolic water or EZ. I have been waiting for papers to link melanopsin dysfunction to a falling dielectric constant in the anesthesia literature but no luck on that so far. I strongly believe these mechanisms are linked. This is why Vitamin C by the IV route can help cases like this. It will not work by the oral route.
Mitochondrial cytochromes are all heme-containing lipid proteins. This would cause acute colony failure of the photoreceptors there. I bet it would alter catalase in the cell as well which quenches free radical signal H202 as well. Catalase is another heme-containing protein. All heme-containing proteins seem to be red light chromophores as well. Hemoglobin is the main red light chromophore porphyrin in our blood. Hemoglobin has a strong ability to absorb light between 250-600 nm. UV light spectra go from 250-399nm in man. The word porphyrin is derived from the Greek word which stands for purple. Purple light is UV light color in the solar spectrum. Again here you see the link back to UV and IR light in these disease mechanisms. B12, folate, melatonin, riboflavin, serotonin, dopamine, glutathione are just a few of the photoreceptors destroyed by ferroptosis. This is why photobiomodulation seems to help in some of these disorders, in my opinion. It helps reverse cell death from this mechanism. Few people are making these links in the literature.
The classical view of cell death has long assumed that, once initiated, the dying process is irreversible. However, recent studies reveal that recovery of dying cells can actually occur, even after initiation of a cell suicide process called apoptosis. This discovery raised fundamental key questions about which forms of the cell death process could be reversible and how reversal is mediated. Recent study results reveal the first evidence that ferroptosis is reversible and they have suggested strategies to enhance its reversibility. We are now using those ideas in helping our clients out at Kruse Longevity Center. bio.biologists.org/content/8/6/bi…
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