TODAY'S LESSON ON SUNGLASSES. UV LIGHT, POMC, and HOW THEY ALL LINK TOGETHER. Ciliary ganglion controls how much light gets into the pupil and it controls the lens ability to refract and target light on certain parts of the retina. This is why a ciliary ganglionectomy has massive effects on melanin production in humans. Wearing sunglasses is a temporary way to give yourself a ciliary ganglionectomy. This is why sunglasses wearing leads to more sunburns. The ciliary ganglion contains postganglionic parasympathetic neurons that supply the ciliary muscle and the pupillary sphincter muscle. Because of the much larger size of the ciliary muscle, 95% of the neurons in the ciliary ganglion innervate it compared to the pupillary sphincter.

Below see the detailed view of nerves of lateral orbit showing the ciliary ganglion immediately behind the globe of the eye.Image
2. Decentralized medicine has a lot to say about how our tissues deal with light and water. The ciliary ganglion is a bundle of nerves, parasympathetic ganglion located just behind the eye in the posterior orbit. It is 1–2 mm in diameter and in humans contains approximately 2,500 neurons. The ganglion contains postganglionic parasympathetic neurons. These neurons supply the pupillary sphincter muscle, which constricts the pupil, and the ciliary muscle which contracts to make the lens more convex. This changes the target of light on the retina and this implies differerent tracts which begin in the retina are targeted based upon the light you chose to live under. Both of these muscles are involuntary since they are controlled by the parasympathetic division of the autonomic nervous system.
The ciliary ganglion is one of four parasympathetic ganglia of the head. The others are the submandibular ganglion, pterygopalatine ganglion, and otic ganglion.

Three types of axons enter the ciliary ganglion but only the preganglionic parasympathetic axons synapse there. The entering axons are arranged into three roots which join enter the posterior surface of the ganglion:

1. The sensory root branches from the nasociliary nerve and travels through the ganglion forming part of the short ciliary nerves. These sensory axons supply the cornea, ciliary body and iris.

2. The sympathetic root originates from the internal carotid plexus with cell bodies in the superior cervical ganglion. I'll have a lot to say on this nerve below in the thread. These axons pass through the ganglion and enter the eye without synapsing into the short ciliary nerves. The sympathetic root contains the postganglionic sympathetic axons that provide sympathetic supply to the blood vessels of the eye that come from the internal carotid artery loaded with melanopsin chromophores. Sometimes, they also supply the pupillary dilator muscle, however these axons usually travel from the nasociliary nerve to the long ciliary nerves to enter the eye.

3. The parasympathetic root branches from the inferior division of the oculomotor nerve and carries the preganglionic parasympathetic axons from the Edinger-Westphal nucleus to the ciliary ganglion. Within the ganglion the axons synapse onto the postganglionic parasympathetic neurons. These neurons project axons through the short ciliary nerves to innervate the ciliary muscle and pupillary sphincter muscle.

Most centralized people do not truly understand what they eye really does for the decentralized organization of the human brain. Let's examine the implications.
4. Why does chronic or short term damage to the ciliary ganglia cause problems related to tanning and solar charge connection? They eye not only sees the light, it refracts it and targets the retinohypothalamic tract that is begins in the inferior nasal part of the retina. Early morning sunlight hits this target as the sun rises higher in the sky. Early in the morning in most places UV light i snot present. UV-A and IR- A show up first and this stimulated the production of nitric oxide in the eye and in the head and neck of humans. This step is important in human melanation. These are DECENTRALIZED things your dermatologist does not even know, but is published in the literature, but your decentralized neurosurgeon does know and teaches you. Be careful who packs your parachute. @JuicefBukele
5. See AM sunlight is the first step in Human melanin renovation. Ultraviolet B irradiation of the eye begins later in the AM and this light energy is transmitted in a nitric oxide-dependent manner through the ciliary ganglia involving the first branch of the trigeminal nerve to the hypothalamopituitary proopiomelanocortin system. If you do not get the upregulation of NO from AM light loaded with UV-A and IR-A light, UVB light becomes less useful to you and in some haplotypes can harm you. Yes, you paleo humans I am speaking to you. The disruption of this set of decentralized circumstances has huge implications. It results in diurnal upregulation of alpha-melanocyte-stimulating hormone secretion every day in controlled fashion and consequent stimulation of melanocytes in the skin. This is really why sunglasses are killers. It also implies why sunscreen is a centralized idea of the profiteers.
6. Now about that superior cervical ganglion and how it links to the blue light non visual photoreceptor, melanopsin.......... Image
7. What connects your inner light creation to your filaments in cells? Is your life electric because your mitochondria in cells make a plasma called water? You do know that your mitochondrial also creates light via metabolism huh? Have you read the book below that shares that data? I know your dermatologist has not read it.
8. Is your filament, called your gut, connected properly to your brain by sunlight and water? Are your brain and gut set up via coherent coupling of cycles between food and light of the day in your retina and brain? You do know food is an electromagnetic bar code of photosynethesis right? The vagus nerve does maintain this "watery connection" between the brain and gut over a water electric network. These two systems are CIRCADIAN harmonic oscillators that need to be properly coupled to work together. Do your centralized experts know this? What connects these two oscillators in our body? Water networks connect them both organs. Why do not centralized experts realize these connections exist in all of us?

9. Sunlight makes the water in our cells a liquid crystalline PLASMA. It increases the amount of electrons in it. Water without deuterium has a high dielectric constant. DDW in the mitochondria is at 160. Water from your tap has a dielectric constant of 78. That means tap water with 150-155 ppm of deuterium in it does not have as many electrons as mitochondrial water and without those electrons sunlight cannot be be absorbed as well. This makes water made in you a BETTER electromagnetic capacitor = BATTERY. That is the battery all cell run on. Your brain has more mitochondria so it makes the water it needs to operate with the sun.......now do you get enough sun to run your epigenetic programs?
10. That water cells need must be created by our colonies of mitochondria and this is how eukaryotes to bring the sea onto a land-based existence. Liquid crystalline = coherent water = a sea of electrons for redox chemistry to exist. Liquid crystalline water possesses long-range orientational order by pointing all the molecules by pointing in the same direction. This is an electric or magnetic polarization effect. It also allows for a translational order that allows them to keep their position as they move = topology effect. Liquid crystals are mobile and flexible and highly responsive to electromagnetic radiation in our environment. This allows them to undergo rapid changes in orientation or phase transitions when energy is added or subtracted from the water. This is why cell water responds vigorously to exogenous electric or magnetic fields.


11. It is why water responds vigorously to temperature, pressure, pH, hydration, and concentrations of inorganic ions like phosphorus. I think the Universe is powered by water electricity and I believe every cell is powered in the same way. CSF comes from the water in blood plasma and then its chemistry is changed by the choroid plexus of the brain by iodine and salt. Salt levels control the physics of the coherent domains of CSF. In my opinion, It is the single most key mechanism in the brain from a quantum perspective. It changes the redox potential of the entire organ. Water is the energy that life runs on. Water is the universal electron and proton donor. When you understand these concepts, you begin to see that proton and electron currents in water made by sunlight create currents inside of cells and over extracellular distances that are capable of delivering physical and chemical messages concerning the redox status of all parts of the cell.
12. I met two guys in August named Dave & Mike recently who did not believe that what is posted in the above slide in yellow was true. This means they do not understand decentralized networks or decentralized medicine.



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13. Water networks communicate this information by way of the vagus nerve. The water in blood plasma is a non-homogenous mix of water that has low UV absorption rate that can be changed as its dielectric constant changes with the addition of salt, anions, and iodine. Once the water in blood plasma becomes partially structured, this fraction of cellular water has better UV light assimilation as its viscosity and refraction are altered. Just adding a bit of salt to this water does this. Your body does this and so does a coconut. This is a clue for those who still remain vitamin D3 deficient despite getting "adequate" sunlight and/or use tanning beds that some other process in them remains lacking. If you do not believe it, you need to read some more. I know your centralized experts aren't on your behalf.
14. Water is redox in humans. Water molecules are more than just made up of hydrogen and oxygen ions. These ions have electric charges and form dipoles. Water is not inert, its ions are dynamic, always rotating and vibrating. Due to the various bonds and kinks that form among water molecules, clusters of water can emit a multitude of electromagnetic frequencies depending on the number of water molecules and their bonds in the clusters. With different structures of water clusters, different electromagnetic frequencies are produced. This means that water can resonate at any virtually any frequency. How does it do this? Water must first absorb ambient electromagnetic radiation to re-emit it. Sunlight can activate oxygen’s outer electrons to higher energy levels and in 0.0000001 seconds, returns to ground level, emitting photons with a frequency of about 1,000,000,000,000,000 Hertz. Water is, in fact, a repository for electromagnetic radiation of all types. The human optical windows, however, operate precisely between 250nm-780nm. Proteins can utilize 200nm -900nm light. Water consists almost entirely of a type of elementary particle called a photon (a photon is a boson and bosons are the glue that holds matter together) and only a very small amount of water is actual matter and it is hypothesized that water is 974,600,000,000 parts photons to 1 part matter (hydrogen and oxygen). Water is mostly photons and photons are the force carrier (messengers of information) of the electromagnetic field. This explains how electromagnetic information is propagated at the molecular level, via water.
15. All biomolecules are dependent on water. We are made up mostly of water, specifically structured, liquid crystalline water, which is imbued with a multitude of electromagnetic frequencies. We are always immersed in a plethora of natural and unnatural electromagnetic radiation in our environments, some beneficial, others harmful and it is constantly changing the liquid crystalline water in our bodies faster than we can think. The ambient electromagnetic environment is literally changing the way living water behaves in our bodies to create health or to fuel disease. This has tremendous implications for biology and medicine.This sets in motion the requisite core of chemical reactions that restore the local and global energy balance of all living things. The vagus nerve is our electric filament, the spark of life, found between seas of water in us. It is that nerve that connects two organs photoelectrically using water as its plasma to make free electrons/protons. Water is present on either end of this nerve. You must become a water muse, first and foremost. The vagus nerve controls the parasympathetic portion of the autonomic nervous system as the picture below shows. It begins in the area postrema of the 4th ventricle. The vagus is part of the parasympathetic system that lowers the stress response. Its activity drops chronically when the sympathetic system is constantly turned on. Your vagus nerve, ciliary ganglion and the superior cervical ganglion all connect via water networks in your brain and none of your centralized specialists know it. Uncle Jack decentralized courses he teaches do.
16. The sympathetic system outflow of the stress stimulus begins in the paraventricular nucleus (PVN). The vagus nerve is the calming portion of the ANS and antagonizes the PVN to lower stress and INFLAMMATION. The vagus nerve is also key in allowing mitochondria to oscillate at 100 Hz to fat burn. Balancing both arms is critical in avoiding diseases, and creating allostasis. Autonomic nervous system (ANS) regulation is a function of light and water properly activating one another to control magnetic flux in the spinning ATPase on the 5th cytochrome. The vagus nerve connects dissimilar "bodies of water" within the human body to make them work coherently. They use the light in that environment to make a connection or allow a mitochondrial disconnection which disrupts energy flows. The stimulus of light on our skin and retina changes the water domains in CSF in the brain and in the gut. 99.8% of CSF is made up of cell water. This is how the “central digital” circadian system from the RPE of the eye, the skin, and gut are linked to the SCN which sits in a cistern of CSF above your optic nerves in your skull. Light waves are transformed to phonon vibrations in the water. When this occurs water becomes coherent and becomes a sea of electrons to run redox pathways in biochemistry properly and coherently. This allows all mitochondria to vibrate as one. The “analog circadian system” of the gut is linked to solar light exposure from food electrons and to the timing of food grown in the environment that cells get in our mitochondria so that the signals can be yoked via the area postrema (AP) and the median eminence (ME) in the brain. These two areas in the brain have no blood-brain barrier. They allow water and light communication to occur, so the electron density in the CSF is accurately tied to the local environment these neurons can sense. Electron density and coolness are linked in water. This is true in the ocean and in our cells and CSF cavities. For example, when we eat, 60% of blood flow is shunted from the peripheral blood to the gut’s mesenteric system by the autonomic nervous system. The brain senses and pays attention to these shifts, using the vagus nerve, as its main information highway. When the sun hits our skin (UVA and IRA light), nitric acid (NO) is released and 40-60% of blood flow raises to the skin surface to become radiated by solar radiation. This energy transfer is sensed by the vagus nerve in our superior cervical ganglion and sent to the brain to lower our stress response in the PVN. This stimulates melatonin cycles to work properly. So if your lifestyle buries the sun, you create a stress response and if you do it long enough you might end up with a disease.
17. Oh and if you think there is not good data on that vagus nerve water connection............psychologytoday.com/intl/blog/the-…
18. Cells are designed to be a repository of collectible wisdom from nature’s energy and information buried in sunlight and geomagnetic pulsations of Earth. That energy and data come to cells as waveforms and their energy and data are stored in water. The energy is coupled in cycles and not thermalized. This is how cells remain far from equilibrium. Given our cellular design to capture and collected and decipher waves, no human being itself should be considered impaired innately, instead, there are environmental shortcomings that cause the impairment. Thus, it is incumbent on the on the clinician to recommend treatment of the environment their patient is in. People react to an inferior environment, way before their genome is altered. We time stamp our DNA after it is translated using sunlight that controls circadian biology. This is why altering you rgenome is a losing centralized idea. That is what the science of epigenetics and ubiquitin biology are telegraphing us, but the modern paradigm is not listening to this data. You must begin to listen to the wisdom built into YOUR nature.
19. Light controls the two decentrlaized networks in the world.........never forget it. See above pic for reenforcement. Image
20. What is the cornerstone blueprint of the human brain? Light, water, and the electromagnetic fields in Nature have built a Superconducting Quantum Interference Device (SQUID) on the surface of your brain that allows us to be human. SQUID’S are important in the mammalian neocortex because they are able to switch signals from one neural circuit to another, at extremely high speeds, while storing massive amounts of information, all while using very low power (20 volts). We are part of an electric universe.
This all can be done in the tightest of quarters in our skull. This works at nanoscopic levels on semiconductor chips in your laptop and in the subarachnoid space of your brain. This is precisely what happens on the human neocortex and explains how the cortex actually can do the things it does. This occurs using quantum principles called the Josephson effect. The 1971 Nobel Prize was given for the discovery of this effect to Brian Josephson. Moreover, the Josephson effect provides the biologic and technologic basis for the development of an ultra-sensitive magnetometer called a SQUID. A SQUID instrument (or biologic tissue) is capable of detecting the magnetic fields produced in spaces in or around the body. Your mitochondrial redox links directly to the signal a MEG records the power density in the fields our mitochondria create.
21. THE DECENTRALIZED LESSON IS OVER. Tag your friends and upgrade their game. It is time we all ADD PROOF OF WORK to our game in life. @hubermanlab @RickRubin @jack @jackmallers @JuicefBukele Image

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More from @DrJackKruse

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…
Read 5 tweets
Aug 16
1. Today's lesson: Your longevity experts are RETARDS.
If you know you know. This is the lady below that shows you every longevity expert out there is FOS. She is and was the ultimate wellness rule breaker who lived 122 years and 164 days. Longer than anyone in recorded history.Image
2. Her daily routine:

↳ Smoked 2 cigarettes daily until age 117
↳ Ate 2 pounds of chocolate per week
↳ Drank Port wine regularly
↳ Doused everything from the Sea/land in animal fats and olive oil

She also took up fencing at 85. Rode her bike until 100. Walked until she was 110. She only quit smoking because she went blind and could not see her cigarette to light it. She was the opposite of this rich moron below.Image
3. The Decnetralized Science Behind It

Her mitochondrial colony were exceptional. She sat out in her flower garden every day of her life. She was a young woman when the Eiffel Tower opened and was present. She was there for its 100th anniversary as a guest of the French government. Studies on her found she had mitochondrial epeigenetic variants that enhanced cellular photo repair and maintenance.

She was the first human who showed us that environment trumped our nDNA and diet. But centralized science continues to miss this lesson and you pay that toll every day with their evidence based advice.

None of you realize it. How can I say this?

Did you know that recently a paper was published in Nature Medicine that was a massive analysis from the UK Biobank on this topic. Do you know what it revealed? It revealed the lesson Ms. Calment life; that our environment – the "exposome" of everything from air pollution to workplace light stress packs a bigger punch on how you age and die than your diet or DNA ever could. It tells us why all our longevity advice is horribly flawed.Image
Read 12 tweets
Aug 7
1. This interaction is governed by the Chiral-Induced Spin Selectivity (CISSS) effect, where spin-polarized photons or electrons preferentially match the protein's chirality. In photosynthesis, this spin selectivity may guide exciton transport through protein complexes. If a biophoton's spin aligns with the protein's symmetry, it can trigger excitation or release; otherwise, the signal may be lost, suggesting spin could be nature's way of encoding selective bio-communication.
2. Mitochondria convert food into electrons via the electron transport chain, where cytochromes (especially cytochrome c oxidase) pump protons out, reducing oxygen to water. Proton tunneling, not just bulk diffusion, enables this rapid proton movement (over 10³ protons per second). ATP production peaks during awake hours and initially rises during sleep onset due to free fatty acid (FFA) release, but drops sharply in REM sleep to support a quantum state for brain recycling.

During uncoupling in deeper sleep, mitochondria release infrared heat, condensing surrounding water and coupling to quantum processes.

This mirrors spintronics, where electron spin, manipulated by electric and magnetic fields, stores information, much like mitochondria control electron spin for energy and life processes. Free radicals, with unpaired electrons spinning in the same direction, play a key role, defying the singlet state (paired spins) governed by the Pauli exclusion principle. This quantum spin manipulation underscores mitochondria's unique bioenergetic role.
3. When electrons with the same spin are excited by electric or magnetic fields, they enhance quantum processes in chloroplasts and mitochondria, which use Fe-S redox complexes as electromagnetic compasses to gauge environmental needs. These organelles act as quantum heat pumps, generating infrared light modulated by free radical signals to drive energy and signaling via the MINOS water layer. Water, with its high dielectric constant, breaks symmetry by separating charges and shrinks when heated by infrared, imprinting environmental signals as an ionic plasma. Its hydrogen bonding network acts as a quantum measuring device, recording the state of entangled electron pairs in free radicals. Mitochondria release monochromatic infrared light to entangle electrons and protons, akin to the double-slit experiment, while skin filters sunlight (optimal at 270 nm UV) before mitochondrial processing, reflecting a quantum-coupled design in evolution.
Read 24 tweets
Aug 7
Why dentistry needs to be decentralized badly: instagram.com/reel/DNDlNR1Ok…
2. Decentralized Answer:
My thesis leverages first principles in your question to me about LPR because light as energy, POMC as a UV switch, melanin as a charge modulator all link to propose that sunglasses disrupt UV-driven biology, reducing melanin and charge, and potentially causing LPR via glycation and neural crest effects. The UV-POMC-melanin link is solid; the LPR and charge extensions are cutting-edge hypotheses needing research.Sunglasses,

UV Light, and Melanin Production: Principle: Light is electromagnetic radiation, and UV photons (e.g., 280–315 nm UVB) carry energy that excites molecular chromophores in skin cells, triggering biochemical cascades. POMC (proopiomelanocortin) expression is a photochemical process driven by UV light, as confirmed by studies (e.g., Slominski et al., 2018) showing UV-induced upregulation in keratinocytes and melanocytes.

Mechanism: UV photons activate POMC transcription, leading to α-MSH production via the melanocortin 1 receptor (MC1R) pathway. α-MSH stimulates melanogenesis, producing melanin, which absorbs and dissipates UV energy, protecting tissues. Sunglasses Effect: Sunglasses with UV400 protection block 100% of UVA/UVB. If UV is the sole trigger for POMC translation, blocking this spectrum halts the signal. This reduces α-MSH and melanin synthesis. The extent depends on exposure time, but chronic use could significantly lower baseline levels, especially in low-pigment individuals. The claim holds, sunglasses directly reduce melanin by cutting the UV-POMC- α-MSH pathway.
3. Ciliary Ganglion and POMC Disruption: Principle: The ciliary ganglion regulates pupil size and lens accommodation via parasympathetic innervation (95% of its neurons target the ciliary muscle). Light spectra influence autonomic signaling, and neural crest cells (originating from POMC-expressing regions) migrate to form pharyngeal and laryngeal structures. Mechanism: UV light, absorbed by retinal and skin chromophores, modulates POMC processing into its 10 peptides (e.g., α-MSH, ACTH). Sunglasses alter the light spectrum reaching the eye, potentially mimicking non-native electromagnetic fields (nnEMF) by shifting the input from natural UV/IR to artificial blue light. This disrupts POMC translation, affecting neural crest-derived tissues, including the pharyngeal pouches. Sunglasses mimic a ciliary ganglionectomy (surgical removal). Sunglasses functionally alter light input, which indirectly influences ganglion-mediated responses and POMC signaling. The nnEMF mimicry is plausible because blue light (400–500 nm) from screens differs from UV (280–400 nm) in energy and penetration, potentially misaligning cellular clocks and POMC processing.Image
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