Month: February 2023

If centralized physicist is correct, and thermodynamic laws for energy say energy is a fixed quantity in the universe, and the speed of light is fixed at the same time, what does it mean when we know there are one billion photons present in the cosmos for every atom in the known universe?

It means light has to be the “Jacquard card” of cellular design……..

What is the function of Jacquard’s card?

In a Jacquard loom one of a series of perforated cards controls the manipulation of the warp threads and determines the intricate pattern woven on the material.

What is a Jacquard loom?

The Jacquard loom is often considered a predecessor to modern computing because its interchangeable punch cards inspired the design of early computers.

The atomic arrangement of atoms in cells is the Jacquard card and the loom is light.  The creation from this interaction is created in the substance of water.  The arrangement of atoms creates the conditions to facilitate quantum coherence in cells to build a quantum computer called your organs.  Each organ is like a member of the orchestra.  Each organ is coordinated by the SCN.

HOW ARE OUR WAFERS BUILT? 

Just as Taiwan semiconductor makes chips through a complex process that requires atomic precision, clean environments, expensive factory equipment, and time, your cells require the same conditions.  Control in Nature’s fab plant is done optically by light and dark cycles.  

Semiconductor device fabrication in the tech world is a multiple-step sequence of photolithographic and physicochemical processing steps (such as thermal oxidation, thin-film deposition, ion implantation, and etching) during which electronic circuits are gradually created on a wafer typically made of pure single-crystal semiconducting material. Silicon is almost always used, but various compound semiconductors are used for specialized applications.  Silicon is a narrow-band semiconductor.  Nature rejected Silicon and chose carbon as her “wafer”

Semiconductors are arbitrarily defined as insulators with band gap energy < 3.0 eV (~290 kJ/mol). This cutoff is chosen arbitrarily because the conductivity of undoped semiconductors drops off exponentially with the band gap energy.  The  3.0 eV level is very low and creates light in the red range.

Nature used carbon and atoms for her semiconductors to create light from the VUV to IR range.  This mirrored the terrestrial spectrum of sunlight on ancient Earth before cells evolved.

Nature also used her own version of a photolithographic method to create her wafers that use circadian biology as her optical tweezers to place atoms at specific locations in cells to gain the desired physiological effect.

Each one of your cells is a quantum computer that is integrated & entangled to one another in their organ and in distant organs in many novel ways.  The basic design of the quantum cell is that Nature built living semiconductors with wide band gaps.

Visible light covers the range of approximately 390-700 nm and corresponds to band gaps of 1.8-3.1 eV

Carbon comes in many semiconductive crystals.  Carbon in the form of a diamond has a large band gap at 5.4 eV.  At a band gap of 5.4 eV, no light in the visible spectrum can be absorbed. These substances transmit all incident light and are colorless in their pure forms.

Our proteins are semiconductive when they are hydrated.  The “wafer design” always uses atoms in the periodic table in Periods 2-4 of the periodic table because most of these metals have band gaps that allow cells to create light in the VUV to IR ranges from atoms adjacent to our hydrated semiconductors.

Human cells only use atoms 1-53 on the periodic table but not all these atoms are used for a variety of reasons linked to wide band gap solid-state wafer design.  Many of these atoms are used over and over again because they have band gaps from 1.5 eV-8 eV.

Collagen is the most common protein of man and it is a wide-based semiconductor.  Collagen types vary in design and so do the dopants on them.  For example, we know that in bone collagen is the N-type wide-based semiconductor, and hydroxyapatite is the P-type semiconductor that has a band gap that emits 200-270nm light.  This is UVC light extends past the light the sun provides at the bottom of the UV light in the visible spectrum of sunlight.  It marries beautifully with the absorption spectra of aromatic amino acids.

Wide-bandgap semiconductors permit cells to operate at much higher frequencies of light in the UV range.  They also can tolerate higher voltages, background radiation, and temperatures than conventional semiconductor materials.  The most critical thing they do for cell design is that Many group 2-4 atoms create wide-band semiconductors that can emit UV frequencies that are more powerful than the sun provides.  This explains two things.  Why did cells use only 4 aromatic amino acids on Earth?  Nature married the band gap distances of atoms to only 4 amino acids with a specific power density UV absorption spectra. This explains the slide I used in Vermont in 2018 and that I mentioned in the QT #26 blog.

What else does it explain?  Roeland van Wijk laid out the case that Pritz Popp found that every cell on Earth emits ultraweak-UV light.  Prokaryotes emit 5000 times more light than eukaryotes but they all emit light.  Guess where their light emission comes from?  Their wide band semiconductors.

Why was light picked as our Jacquard punch card by Mother Nature?

From above I told you that Jacquard built the first computer that used punch cards to make silk patterns using a binary pattern using the loon.
So how did Mother nature build her first computer called a cell?

In our universe, there are one billion photons for every atom.  That is the light-to-atom ratio. So she chose to use the higher quantity energy asset so she started with light from our star. She realized 4.6 billion years ago that this light contains both energy and information at a ratio of a billion to one. That was the bandwidth she had to work with.  Of the two Mother Nature was the first to realize that information in light could be used to organize the matter.  The atomic organization is the basis of design.

It took until Maxwell’s paper on demons in the 1860s, for anyone else to realize this relation between photons and atoms existed.  No one knew what it meant much less implied.

Light is the “bit” cells use to transfer information. Information is buried in the orbital angular momentum of light (OAM) of light. The energy in light is buried in its frequency.  Immediately Nature realized that low-frequency light packed quite an information punch.  That punch was formulated into a card we call a cell.

Since there are one billion photons per atom energy and information has to flow from light to atoms.  A billion-to-one ratio is like asking a 20,000 waterfall to reverse its flow without adding a bit of energy.  Kight cannot flow the other way, just like a waterfall cannot flow in reverse.  This set the parameters for the arrow of time creation.  The entropy measures the flow of light in a particular atomic organization.  The ratio gave time an arrow.  Clocks were innovated to count the flow of entropy on these ancient semiconductive cell-wafers.

With this circuit board arrangement, there is no way for matter (atoms) to transmit information or energy to light because of this primordial ratio. This means that atoms are the hardware of the computer and light is the software that runs the computer.

It also means information and energy move from light to matter all the time because of the second law of thermodynamics.  Now you can begin to see how the classical world you call reality is glued to the quantum level by the laws of thermodynamics.

Why did she choose light as the key in her design?

Light is the ONLY particle that seems to have an unlimited amount of orbital angular momentum (OAM), and OAM = information.

The same thing is not true about electrons or protons. The OAM of both are limited by the laws of physics.

Information by itself is capable of creating order from chaos.  I have a blog coming up on those details.  This happens because our cells are built to store information at the electronic level in every part of the circuit board.  This made cells a dissipative structure.  Light information creates a memory in water.  It is buried in its coherent domains and in hydrogen bonds. Proteins suspended in this cell water are critically important to our wafer design.  The ATPase, melatonin, collagen, NAD+, leptin, and melanin are critical in her designs.

Water can absorb massive amounts of OAM information but water does not cover all frequencies in its absorption spectra.  Many of the chromophore proteins I just mentioned can and do help water out with light absorption. This is why you will see melatonin, water, and melanin in close proximity in critical areas of human biology.  Just think about the leptin-melanocortin pathway as a proxy for this idea.

Human neuroectoderm was a spectacular addition to the primate clade in their brains.  Mammals are 210 million years old and they were able to figure out how to use charge density changes to move melanin from their hair into their brains over 210 million years.  It was perfected in ancient humans to sculpt their brains.  Changes in the environment sculpted these moves.  You’ll be hearing about them soon.

One of the problems with wide-band semiconductor design with time is, light information will fill the capacity of all the electronic states inside the cell and fill up all the memory slots.  When this happens memory space would decline. Information can only be useful on an ongoing basis until memory deletes information contained in light/water.  Cell developed a plan for this called sleep.

KEY BLOG MOMENT:  The erasure of information is what drives entropy increases over time. This is a consequence of having 1 billion light photons to one atom ratio in the universe.  Cells somehow figured out how to use visible light to transform matter into more powerful light and then turnaround and use this transformed light to make water flow uphill.  Mother Nature used the periodic table and solid state physics as her cosmic wand of creation.  This is the basis of how cells create a negative entropy state.  This created the appearance that life somehow was breaking the second law of thermodynamics.  It wasn’t.  She used semiconductors to create better sunlight than the sun shines on Earth.

ATPase creation

Adding sunlight chronically to cell water makes the dielectric constant go from 78 to 160.  In ancient times when more dangerous parts of the electromagnetic spectrum in the dielectric constant were likely higher.  This gave ancient cells the ability to add a ton of OAM to water to build better optical tweezers to build the ATPase. What were the collateral effects of having an excess of sunlight interacting with atoms for a billion years before life organized?  The hardware could be built using that excess OAM locked into the electronic state of the cell.   It turns out the ATPase was created and it optimized its operation to light from the environment.  It was quantized to these changes.

Under the power of non-flickering red light from the sun, the ATPase becomes a 100% energy-efficient nano-torque motor. Researchers are now adding chemicals to cells that can monitor torque speeds like an anemometer measures wind speeds on a barn. To measure the micro-viscosity inside a cell, the researchers first needed to create and insert the measuring protein. This allows them to understand the hydrodynamics of how the created probe behaves diurnally day and night as the environment varies.

Different electromagnetic environments should create different viscosities which alter the tensegrity of the system. Once you alter the shape you alter the charge and this is how redox varies inside a cell. Using computer simulations of liquids, the researchers were able to show that as the viscosity of the solution increased, the rate of rotation of the probe decreased and its fluorescence changed in a measurable way.

CREATION OF ELF-UV LIGHT

So it appears increasing the viscosity of cell water by light addition increases the coherent domains in water, while lowering the number of protons, which raises the net negative charge inside the cell.  Storing powerful VUV light at the electronic level allowed cells to develop mechanisms to create ELF-UV biophotons. This is the kind of paper a Black Swan loves. It undercovers the recipes of Mother Nature for the ignorant to see.  https://pubs.acs.org/doi/10.1021/acsnano.8b00177

CREATION OF THE ATPase CREATED THE ABiLiTY FOR QUANTUM COHERENCE IN ORGANISMS AT A CELLULAR LEVEL

The reaction that turns molecular oxygen (O2) into water releases lots of energy inside cells, and all complex life cells needed that energy to drive their bodies functioning. The half reaction and associated free energy change are:

O2 + 4H3O+ + 4e- –> 6H2O     delta G = -305 kJ/mol

There has to be a biological mechanism for capturing oxygen as O2 in its high-energy, zero oxidation state and bringing it to “a place” where it can be turned into H2O.

THAT PLACE IS YOUR COLONY OF MITOCHONDRIA

The ATPase is a CARNOT HEAT ENGINE in mitochondria that is the ultimate wide band gap semiconductive device in a cell.  Here are its key DYNAMICS: Cytochrome c oxidase creates its own water.

Every 3.5 times the ATPase spins one molecule of ATP is made. Only the H+ isotope can spin the ATPase. Deuterium cannot spin the ATPase and in many tissues, it destroys it. Each molecule of ATP in a cell controls 8,800 water molecules binding sites and 20 potassium ions to make a liquid quasi-crystalline semiconductor inside every cell of our body.

K+ is usually in solution with a Group 7 atom like Cl. KCL has a massive band gap. This entire crystalline structure of water is built by deuterium depletion of the mitochondrial matrix at cytochrome 4. This chromophore has 4 red light photoreceptors and it has a heme proteins in its core.

All these are destroyed by free retinal from melanopsin dysfunction. As melanopsin damage occurs it frees retinal and the retinal destroys the atomic arrangement of melanin and heme proteins where ever they are suspended in cell water. This damage needs to be repaired or disease will result.

Chemical and atomic structural disorder profoundly influence the steady-state spectroscopic properties of heme proteins and melanins. The consequences of the of atomic disorder of wdie band semiconductive proteins is called disease generation.  This includes redox disorder on excited solid state dynamics.

What do you think that would do to the normal ratio of deuterium to protium in a cell even if you knew nothing about biology? It is common sense. As deuterium flows into the matrix less ATP is made. As less ATP is made we get diseases and come closer to death. This is exactly what cyanide does at a faster time scale and people want to act like tech screens are “safe”. This is a freaking joke to those of us who understand biophysics of what “P” is doing really in ATP inside the quantum cell.  It is not what is published in any biochemistry book today.

AMP/ADP/ATP are all wide-gapped semiconductive proteins and “P” dopes them to fluoresce. Read the Lavender blog on LinkedIn now. Carefully re-read the Quantum Thermodynamics #26 blog on Patreon again. Why is it that the few amino acids cells use have VUV light absorption spectra?  Where was that light coming from?

This deep VUV light interaction with matrix water is how a cell uses light and water to create coherence inside every cell in your body.

In the living state, potassium acts like “a solar glue” to keep our protein backbone and water in a quasi-crystalline gel state inside our cell to maintain the semiconducting plates together in a cohesive form in tissues over long distances. This crystalline structure allows proteins to semiconduct and it also limits atomic motions to facilitate coherence. This is why K+ is critical in setting the redox potential of water in a cell.

Hypkalemia in labs is huge tell to a quantum clinicians.  The symptoms in diseases are devasting when they occur.  A low potassium level in a cell has many causes.  It is almost always due to a loss of the atomic arrangement inside cells. Hypokalemia usually results from chronic vomiting, diarrhea, adrenal gland disorders, or use of diuretics. A low potassium level can make muscles feel weak, cramp, twitch, or even become paralyzed without neurologic disease, and abnormal heart rhythms develop.  Left untreated death will occur.

Look at the periodic table above, notice the location of atoms that cells reuse over and over again. In this way, you are building a special type of semiconductor that forms THE REAL “the fourth phase of matter” in cells that emits its own SPRECTRA of sunlight.

It can do this when the surface is perturbed to action by light and then the party gets started inside the cell and can act like a “topologic insulator”(TI). A ‘TI’ allows a multitude of quantum effects to happen in warm wet environments. Modern physics struggles to wrap their belief system around this cellular design.  Yet, they know photosynthesis is run this way since 2007.  This idea offends the core of classical standard physics but even they are coming around to this issue. Look at how they are studying melanins now to make new solar panels.

Silicon Valley types are using narrow-band semiconductors to build tech empires while nature is building-wide band semiconductors where ever you look. K+ changes the optics inside of a cell which allows it to use OAM in VUV-IR light. That spectrum is more powerful than the sun’s spectra is on the surface of Earth. Every critical protein in man is made from aromatic amino acids. Potassium, Na, and Mg will be close to most of the most critical semiconductive proteins in cellular design.

The Fo base piece of the ATPase is embedded in the mitochondrial inner membrane and is a molecular turbine driven by the transmembrane proton gradient. Proton entry forces a central camshaft to rotate within the Fo baseplate and the F1 head group, altering the subunit conformation as this movement takes place. These actions create a magnetic field when there is enough current coming into the inner mitochondrial membrane. When the current is high the magnetic field mitochondria makes is also strongest. When UV light is present and it slows ECT flow, the magnetic flux in mitochondria drops. This is why the DC electric current varies from wakefulness and sleep. We can measure that as Dr. Robert O. Becker did in the DC electric current in neurons in the brain.

A second, off-center protein tether connects the head group to the base piece and prevents the headpiece from spinning uselessly as the central shaft rotates. Energy is transmitted to the catalytic subunits in the ATP synthase F1 headpiece by the rotation of the camshaft. The “cam” distorts the protein subunits (affects light release as a diode/piezoelectric/flexoelectric), destroying their ability to bind ATP.

Piezoelectric release DC electric current and flexoelectricity is the electromechanical coupling between mechanical strain gradient and electric polarization or vice versa. This is how refractive indices in cells are controlled to deal with variable light conditions on Earth.  Cells are capable of changing their dielectric constant by changing the ratio of deuterium to hydrogen in water.  They use mitochondrial uncoupling proteins to do it.

The “P” in ATP responds just as two magnets do when you try to push them together. How? The oxidation state is altered to change its magnetic effects. The energy input is used to drive ATP release, not for bond formation.  Hemoglobin does the same thing when it alters the oxidation state of iron atoms in its core.

It is presumably necessary to disable the catalytic mechanism on the center which has just formed ATP (to stop this center from hydrolyzing its own product) before destroying its ability to bind ATP. This allows the product to be released. Meanwhile, the two other active centers are performing their own parts of the catalytic cycle. The three active centers operate simultaneously but are 120 degrees out of phase.

Because of this, it takes at least 9 H+ protons (possibly as many as 12) to drive one revolution of the camshaft and produce 3 ATP molecules. One turn requires about 3.4 H+. Red light is the main energy source to spin this Fo head and move protons.

HERE IS WHAT EVERYONE FORGETS: Remember that the whole ATPase complex is reversible. Electrons can actually flow from cytochrome 4 to 1 and the ATPase can spin the opposite way. What controls the motion? The electromagnetic force of light does. This complex is optimized to work with UV and IR light and not any other frequency of light. This was a critical understanding when I built my leptin Rx series of blogs.  This is even a bigger deal in a blue-lit 5G world.
https://arxiv.org/abs/1508.06135

SUMMARY

True friendship is like fluorescence, it shines better when the situation darkens.  You might use this description for the greatest event in the history of mammals too, the KT event.  Dark wide band gap semiconduction was critical in understanding the story of leptin.  You will soon understand it all at a very foundational level.  You had to learn many parts first to understand the whole.

Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation. It is a form of luminescence. In most cases, the emitted light has a longer wavelength, and therefore lower energy, than the absorbed radiation. Cells built themselves to take in lower-powered visible light of the sun and used wide band gap atoms to create her wafer design in cells.  This is the basis of why cells seem to have a negative entropy to them. That book written in 1944 made this case. (below).  Schodinger had no idea how it happened and this blog just gave it to your for the cost of a cup of coffee.  That is a decentralized trade.

The most striking example of fluorescence occurs when the absorbed radiation is in the ultraviolet region of the spectrum, and thus invisible to the human eye, while the emitted light is in the visible region, which gives the fluorescent substance a distinct color that can be seen only when exposed to UV light. Phosphorous does the best.  Fluorescent materials cease to glow nearly immediately when the radiation source stops, unlike phosphorescent materials, which continue to emit light for some time after.

Cells have the uncanny ability to emit light close to 150nm based on the atoms we use in our cell design.

What is the implication of this blog?  Many things we believe in centralized science are not only wrong, but the meaning is also 180 degrees from what is printed in textbooks.

Here is the decentralized lesson for this blog for you to consume:

We know from A. G. Gurwitsch’s work on onions and from Popp’s work on cells that UV light is required to stimulate a cell on Earth to divide at mitosis in the cell cycle.  Most centralized cancer doctors believe that cancerous cells are most deadly at the mitosis stage of the cell cycle and this is why chemotherapeutic drugs are designed to screw up the mitotic processes.  This is 180 degrees opposite what you should do!!!   If you understood the blog well, you’d realize why we cannot and will not solve cancer with this pathway of thinking.

We have no Earthly idea how a cell really operates.   You do now.

When a tissue loses its ability to create ultraweak UV light because the atomic arrangement of your wide band gapped melanin semiconductors are demolished from low redox processes like blue light and/or nnEMF human cells cannot undergo mitosis.  The cell is stuck in a non dividing state without UV light.  Moreover, this stoppage of the cell cycle is actually when cancers become lethal via metastasis. On the surface when you say these things to a medical oncologist they think you are nuts.  This is completely counterintuitive position to take compared to centralized teachings.  Today in 2023 some oncology researchers are reporting new data that supports my quantum thesis of cell design that takes account of Gurwitsch’s finding from 1923 on UV light and mitogenesis.

Now you know why I love sunburns and why they don’t matter either.  You are a creature that loves and is organized around Very deep UV light.  That light REGENERATES every wide based semiconductive protein in your body.

CITE

https://journals.lww.com/oncology-times/fulltext/2019/01050/non_proliferative_cancer_cells___the_deadly_charge.5.aspx

Game, set, match.

For the ignorant people advocating sun creams on my social media feeds, & this post should be called your shut-up juice.  Sunscreens have several effects and none of them are good for your decentralized life. Read them below.

1.  The tyrosinase inhibitors block melanin production everywhere in your body and this atrophies the skin (chronically pale), gut (blocked VDR), eyes (RPE) hearing (cochlea/hearing loss/tinnitus), brain/basal ganglia (dopaminergic neurons/PD/depression/suicide/poor executive functioning/poor thinking)

2.  Without melanin in your skin you burn faster BECAUSE your skin cannot make POMC, melanin, and can’t make Vitamin D3 from cholesterol esters. This is why I looked pink above.  It only takes me a few days to repair this problem when I get my skin and eye back in nature.

3.  Unlike most mammals, which have melanin-producing melanocytes predominantly in the hair follicle bulb, humans are uniquely equipped with melanocytes in the outermost layer of the skin, the epidermis. These neural crest-derived melanocytes are the only source of the photoprotective pigment melanin in human skin.  Melanin absorbs UV light and stores its photonic power created in daylight to be transferred to other semiconductive proteins in dark.  These cells are stimulated by 3 pathways.  The UVB, UVA, and the melanopsin pathway.  Of the three, the last one is associated with many human skin/brain diseases.  The second one (UV-A pathway) works with encephalopsin/neuropsin (OPN3).  In humans, encephalopsin works with POMC cleavage protein α-melanocyte stimulating hormone (α-MSH), an agonist of the Gαs-coupled melanocortin 1 receptor (MC1R) that is primarily expressed on melanocytes.  Melanocytes are the cells that cause melanoma.  Blue light is highly stimulatory to melanocytes.  Implications?

Sunlight reduces the incidence of the diseases below.  This means sunscreen will increase them.  

SUNSCREEN CAUSES MORE SKIN CANCERS OF ALL TYPES: HIGHER MELANOMA RISK = LOW MELATONIN, LOW DOPAMINE, LOW VIT D LEVELS = NO SUN = LOWERED mitochondrial REDOX

OPN3 is a negative regulator of melanogenesis in human melanocytes. It lowers the action of alpha MSH and this lowers melanin production.

^^^^^This means another form of light is the real problem.  BLUE LIGHT/nnEMF is that answer.

4.  SUNSCREEN USE CAN DEPRESSES YOUR MOOD and cause depression. It lowers your mood. When you affect tyrosinase inhibitors you also block POMC.  Many will look at the comic below and laugh and find humor in it.  Some of us, however, will see something else more concerning and educational about sunlight.

We might see a story of how nature built us, and why we have a massive opiate issue.  UV-A has a big surprise function that is buried in this picture below: It increases POMC from the brain and protein stimulates many important things.  β-endorphin is one of the more important ones.  Do you know what it does?  It is an endogenous opiate made when we are in the sun.  What happens when you aren’t in the sun?  Think Kurt Cobain, Jimi Hendrix, and Micheal Jackson.  More on this link below.

Melanin provides protection of structures in and below the skin against free, UV-induced radicals. Thus, melanin acts as a direct shield from UV and visible light radiation. UV radiation causes a stimulus to DNA damage in the nuclei of keratinocytes that are degenerating on the surface of the skin.  This results in the activation of the p53 gene, which transcriptionally upregulates the expression of the gene encoding proopiomelanocortin (POMC) mentioned above.  Most think solar radiation induces only bad secondary effects but here is an example of positive regulation. Why do I say this is a positive stimulus?

The POMC precursor polypeptide is processed into several bioactive products, including α-melanocyte-stimulating hormone (α-MSH), adrenocorticotropic hormone (ACTH), and β-endorphin. These all link to important systems. After secretion, α-MSH binds to the melanocortin 1 receptor (MC1R) located on melanocytes and activates melanin production, and is tied to the leptin-melanocortin system tied to obesity. The leptin-melanocortin system was behind the construction of the leptin Rx 12 years ago.   This is why a lack of sunlight is linked to obesity because of a lack of UV-A and IR-A normally present in the morning sunlight. The anti-inflammatory effects of α-MSH and ACTH may help relieve irritation and local inflammation in UV-exposed skin acting as a calming influence. This increases histidine in the skin. (see below)  Urocanic acid is our natural sunblock that I spoke about in the solar callus blog.

Histidine is an aromatic amino acid that absorbs massive amounts of UV-A light. This lowers erythema production in the skin.  It turns out that IR-A light also pre-treats the skin to lower inflammation. The fact that UV-A light induces a small opiate response tells us nature is trying to addict us to get us to come out into the solar light for a REASON.  You should not mess around with that reason.

5. With sunscreen you are raising your risk of hypertension and stroke!  Why?

One amazing way to lower your pressure is with SUNLIGHT via multiple mechanisms.  The first way is via the release of NO in the skin which allows for the blood to get irradiated by the sun via dermal pooling as NO dilates the blood vessels under your skin.  This lowers resistance to lower pressure.

Did you know 40-60% of your blood volume moves toward the sun with this effect assuming you have no clothes or sunblock on? The second way sunlight lowers BP is via the renin-angiotensin system in the kidney. Sunlight raises Vitamin D3 in the skin and blood plasma and this directly affects the inhibition of renin activity in the kidney to control blood pressure centrally in the brain. The vitamin D3 and sunlight axis work via calcium signaling and this gives the endocrine system a potentially bidirectional and stimulatory relationship between aldosterone and parathyroid hormone. Most modern humans have lost this bidirectional control because of clothing, sunblock, and an indoor existence and this is why high blood pressure is now a global epidemic.

6. You always hear the Zen/food gurus talk about the third eye.  The Black Swan mitochondriac reality is that your skin is your literal and figurative third eye if you have not figured it out yet.   Melanopsin was found to be in our eyes in 1998.  Then we found it in the arterioles of our skin in 2014.  Then we found it in our skin and subcutaneous fat in December 2017.  This is when it became clear why so many people in the LCHF community remain fat and cannot tan because their skin is chronically atrophic from blocking the sun.  They have no idea how melanopsin works to explain their phenomena.  In fact, their old leader Mr. Jimmy Moore is a textbook example of what happens when you eat lots of fat and use blue light to run a life.  He regained all his weight and was just sentenced to 20 years for pedophilia with a 13-year-old girl.

Yes, sexual deviancy is something we SHOULD expect in people when they chronically block the sun in how hormones are created in the skin/eye/brain.  We’ve known about this for over 100 years. (see below) .

The implications of this are seen every day now in the pronoun warriors online.  Kids are now bathed in blue and nnEMF in schools.  It is also supported by centralized systems in healthcare now too!  Hospital systems are raking in profits over it.

7. We’ve known about blue light reflecting off the moon for ages.  It is where the word “lunatic” comes from.  Blue light at night makes humans act differently than one would expect because it alters our dopamine levels.  It also affects our sexual functioning and our libido.  It can drive aberrant behaviors as well.

Blue light has been used positively in biology as well at night. Not in humans but if you are a coral.  The problem is modern humans who use sunscreen are killing coral reefs everywhere.  Why?  The sunscreen floats at the top of the ocean.  It blocks the effect of blue light reflected off the moon.

Why is this a big deal?

Starting with the beginning of the last century, a multitude of scientific studies has documented that the lunar cycle times behaviors and physiology in many organisms. It is plausible that even the first life forms adapted to the different rhythms controlled by the moon. Consistently, many marine species exhibit lunar rhythms, and also the number of documented “lunar-rhythmic” terrestrial species is increasing. Organisms follow diverse lunar geophysical/astronomical rhythms, which differ significantly in terms of period length: from hours (circalunidian and circatidal rhythms) to days (circasemilunar and circalunar cycles). Evidence for internal circatital and circalunar oscillators exists for a range of species based on past behavioral studies, but those species with well-documented behaviorally free-running lunar rhythms are not typically used for molecular studies. Thus, the underlying molecular mechanisms are largely obscure: the dark side of the moon.

Lunar rhythms of light, dark, and gravitation changes cause alteration in the human transcriptome, proteome, and physiology.  The proxy for these effects is seen in the hormonal variation of humans.  This can be positive or negative.

The POSITIVE: Lunar cycles modulate the estrus cycle because the moon can and does reflect light from the sun at night to the Earth as it goes through its revolutions monthly around Earth……..that is why they influence woman’s hormone cycles assuming she is properly connected to Earth, sun and the lunar cycles.

A NEGATIVE: MOST ladies aren’t properly coupled to light and dark cycles now, therefore, their hormone effects are muted and lowered in modern females. This is why estrus vanished in humans and proof it still has influence can be seen when women get together and live together their cycle will all become coupled oscillator again…….just like molecular resonance predicts.  When the negative and positive feedback loop is uncoupled from one another the result is the extinction of both sides of the coupled system.  This extinction effect manifests in the pregnenolone steal syndrome that can cause sexual and gender identity issues.

ANOTHER POSITIVE: Among all, probably the most spectacular and documented event orchestrated by animals according to the lunar cycle is certainly the mass spawning of corals. Like inside a shaken snow globe, once every year, the barrier reef explodes with eggs and sperm, a few days after Full Moon, during late spring/summer nights, a phenomenon even visible from space. Unfortunately, reef corals are losing this critical reproductive synchrony, likely due to the anthropogenic impact of artificial light at night. This phenomenon threatens several species, not only corals but entire reef communities.

This is why Mexican cenote owners require humans to take showers before they enter any CENOTE in Mexico.  They want you to remove the sunscreen so you do not harm the life inside the cenote.  Imagine that.  Sunscreen is not good for cenote life either.

8. All these effects have butterfly effects.  How long will it take for people to wake up to how big a deal this is?  Melanopsin serves an important role in the photoentrainment of circadian rhythms in ALL mammals but especially humans.  Why?  Humans have the weakest covalent bond in melanopsin to retinol. This means the bond is easily broken by blue light which is the light modern humans now live under and within >90% of the time. An organism that is photo-entrained has aligned its activity to the 24-hour cycle, the solar cycle on Earth. In mammals, melanopsin-expressing axons target the suprachiasmatic nucleus (SCN) through the retinohypothalamic tract (RHT), skin arterioles, skin, and subcutaneous fat.  In fact, it has recently been shown that the human brain has far more melanopsin in it than any other mammal on Earth.  Humans are the ultimate solar mammal and this explains why the silly-talking monkeys lost their hair/coat.  How do you like that as a game changer?  This implies the food is not what fattens us today.  It is technology that does it.

How? You get fatter because of the blue light way faster than eating carbohydrates.  And when you do that weight is HARDER to lose.

Aponte found that artificial light via the eye over stimulates pro-opiomelanocortin (POMC) and agouti-related peptide (AGRP) neurons acutely regulate feeding behavior. This causes apoptosis or cell suicide of these neurons.  Once this happens you become resistant to the action of leptin.  Aponte found that AGRP-induced hyperphagia is completely independent of melanocortin signaling.  This told us that blue light alone, without red and UV light, could cause obesity. This has been confirmed by electrophysiology studies that have shown that leptin stimulates POMC neuron firing (Cowley et al., 2001) and regulates the activity of potassium channels in POMC neurons thus modulating neuronal excitability (Jobst et al., 2004).  Sunscreen, sunglasses and glass in windows all cause these light effects because of how they block light.  Just living indoors behind glass will fatten you.  It will cause other diseases as well.

Solar exposure with full terrestrial sunlight 250-760nm)  uncouples respiration from ATP synthesis via its NO effect on cytochrome C oxidase in mitochondria.  Uncoupling respiration from ATP synthesis or increasing ATP hydrolysis restores NAD+/NADH homeostasis and proliferation even when glucose oxidation is increased.  UVA light from the sun creates Nitric Oxide to slow Electron chain transport flow mimicking calorie restriction.  The sun however, always has IR-A light present when UV-A light is present, and 43% of IR-A light directly and simultaneously affects the 4 red light chromophores in Cytochrome c oxidase in mitochondria to create water and make ATP without ELECTRONS.  Electrons come from food.  If you slow ECT down you do not need to eat as much.  You can still transform energy because the IR-A light is always present when the sun shines on you.

Any rapid activation of oxygen consumption inside of the mitochondrial matrix leads to local transient hypoxia (NAD+ drops), causing cytochrome C oxidase to change from reducing oxygen with electrons to catalyzing the formation of nitric oxide.  NO disrupts and lowers ECT flow.  Red light can counterbalance NO release by near-infrared light (600-1000nm).  These photons directly energize cytochrome oxidase (Complex IV) via photon absorption, facilitating its catalytic activity and leading to the up-regulation of cytochrome oxidase levels. People seem to forget that cytochrome c oxidase contains 4 red light chromophores in the IR-A range.  The sun is loaded with this frequency of light because it comes from the atomic spectrum of hydrogen.  In fact, it is the most abundant light in terrestrial sunlight. (43%)

When you put sunscreen or sunglasses on you are making it harder to lose weight and easier to gain it while atrophying your skin and eyes making them more susceptible to damage because there is no melanin present in tissues to absorb UV light.

Weight loss factoid of the day:  most people want to argue that it’s an argument between competing theories:

1. The calories in calories out theory (CICO)

2.  The insulin theory of obesity.

My point is simple, both miss the mark in a large way because they never consider light’s effects on the mitochondrial engines.  Nothing makes sense without understanding the power of light in a reversal of obesity because of how solar light controls the chemicals that optimize our engines.  Melatonin, dopamine, and insulin are those chemicals.  These molecules, and not the fuels we eat are critical in engine optimization.  Melatonin controls autophagy and apoptosis, dopamine with melatonin controls photoreceptor regeneration, and insulin improves or destroys the periodicity of the molecular clocks of the gut organs.

Higher blood glucose and insulin levels are seen in poor sleepers.  Poor sleepers have lowered melatonin/dopamine levels.  How is insulin disrupted? Insulin reduces Bmal1 transcriptional activity by altering liver clocks but lowering the periodicity of the clock mechanism. This signaling mechanism has a central role in the initial phase during food entrainment resetting of the hepatic clocks.  It is disrupted by light or food eaten outside of the control of the sun’s light and dark cycles.

Food only becomes a dominant player when the solar light is subtracted or artificial light/nnEMF is added to your life to subtract from the quantized equation on our skin and eyes.

https://jackkruse.com/time-17-melatonin-insulin-solar-metronomes/

See, I’ve been telling you the same story over and over again and trying to get you to understand and stop blaming food for what light causes.  Engine destruction by light always trumps a fueling problem in the engine.

9. Can sunscreen make your migraine headache worse even when you are on medication?  YEP.  How?  When you put sunscreen on you destroy melanin production.  You need melanin production in the RPE of your eye. The RPE of your eye help regulates the function of Muller cells in the retina.

Now we have similar data developing on migraines that light disruption causes brain-level migraines: These headaches result from a stroboscopic effect via the Muller cells into the hypothalamic pathways of the brain and decreased current in DHA and CSF superconductors anterior to the SCN.

The stroboscopic effect occurs when a flashing light source illuminates a moving object. This effect, created by the flickering of the surrounding light, is harmful to the vision and causes discomfort, visual fatigue, and headaches.  Fluorescent & LED are the lights associated with this effect most.

Researchers used H2 15O (radioactive water) to measure regional cerebral blood flow as a surrogate marker for neuronal activation.

They found that compared with baseline scans, there was activation in several key areas, including the hypothalamus, an area involved in low-level regulation of sleep, appetite, mood, and fluid balance. “It seems very likely that the hypothalamus is pivotal in the onset of migraine”

http://ow.ly/mHqV2

10. In mammals, the eye is the main photosensitive organ for the transmission of light signals to the brain because their skin is usually covered by coats and hair.  Humans are unique among mammals as they have shed most of their hair and the skin is their LARGEST organ.   This helps explain why there is so much melanopsin in the human brain compared to hairy primates who cannot talk.  The skin and brain both come from the same tissue in the human embryo called neuroectoderm.  This is why blind humans are a very interesting cohort to follow to learn about how melanopsin and vitamin A work to lower Vitamin D production and POMC production because of altered skin signals humans get from their skin to ruin every peripheral clock gene in every organ of their body by blue light exposure.  Why?  Blind humans are still able to entrain to the environmental light-dark cycle, despite having no conscious perception of the light via their retina.  How do they do it?  They use their third eye in the skin to do it, their skin.  One study exposed subjects to bright light for a prolonged duration of time and measured their melatonin concentrations.

Melatonin was not only suppressed in visually unimpaired humans but also in blind participants, suggesting that the photic pathway used by the circadian system is functionally intact despite blindness. This was a big clue there was another pathway that the circadian mechanism works with.  When it was found that all human opsin were loosely bound to opsin then the connection to mitochondrial dysfunction was easy to make because melanopsin and Vitamin link to mtDNA repair via the production of melatonin.  Melatonin is well known to repair mtDNA damage at night during sleep during autophagy.   This is why in neurosurgery we have warned ophthalmologists, that we should no longer routinely practice enucleation of blind patients or removal of the eyes at birth since the eyes play a critical role in the photoentrainment of the circadian pacemaker and the peripheral clock genes in every tissue in the body.  This also means if you wear sunscreen you are blocking massive information to control all your peripheral clock genes.

There is some good news: If you had Lasik surgery or cataract surgery this is how you help offset the damage to neuropsin in the cornea and/or the blockade of light in your eyes by the intraocular lens the eye doctors inserted to replace your cataract.

https://www.news-medical.net/news/20120522/Study-finds-large-amounts-of-melanopsin-in-the-human-brain.aspx

11.  More on melanopsin, your eyes, and Parkinson’s disease. This is due to the effect of free retinal from its weak covalent bond to melanopsin due to unopposed blue light and nnEMF in manmade light.   The effect is massive and few seem to realize it.  Your pupillary function can be destroyed via your skin and subcutaneous fat.

https://www.nature.com/articles/s41598-018-26078-0

12.  Based on #9 you probably have figured out that the number one cause of cataracts in the 20th and 21 century is now linked to blue light exposure from tech screens and TV.  It also causes dry eye, depression, mood disorders, AMD, hormone problems, and the list goes on every year.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288536/

13. The more sunscreen, makeup, foundation, and skin products you use the more melasma you will get.  The risk increases when you add blue light from indoor living where full-spectrum sunlight is absent.  Melasma is a complex skin issue tied to nonlinear optics and free radicals. It is a circadian mismatch in the skin that releases excessive light from the keratocytes of the skin which in turn stimulates the melanosomes to darken. The reason this occurs in my opinion is that melanopsin is operational in skin and fat. This is a prediction I have made for some time. 

Artificial blue light exposure darkens, freckles, and causes mitosis in melanosomes to lead to darkening diseases like melasma and melanoma. Few dermatologists realize that man-made light is behind these diseases and they should at least consider it. Decreasing tyrosinase activity is a great prevention strategy for conditions related to hyperpigmentation of the skin, such as melasma. Sunlight does this because it is a tyrosine kinase inhibitor. This specific sensitive environment found in your skin and around your mitochondrial membranes is required for the proper release of UV light from skin cells.

It is also related to the mitochondrial function of skin in another way: One cannot make the normal free radical signal in a hypoxic or pseudohypoxic state (low NAD+).  All sunscreens lower NAD+ in your mitochondria.  They cause photoaging.   

UV light increases oxygen levels (and deuterium in the dead skin to get rid of it) in the skin in presence of RBC When full spectrum sunlight hits our skin blood flow in the skin will rise.  Porphyrins in hemoglobin absorb UVA, UVB, and IR-A light.  They have no mitochondria.  Putting sunscreen or sunglasses on your eyes blocks this light.

In melasma, it does not work this way because women are blocking the darkening skin from full spectrum light with their makeup and exposing their skin to man-made light at night. This means we need a constant source of O2 and UV light to keep oxygen as our terminal electron acceptor in the mitochondria of the skin/cornea.  This is why contacts are problem.  They lower oxygen tensions in the eye.   

If we don’t use oxygen as the terminal electron acceptor on the skin it favors the growth of bacteria in the skin/eye.  These bacteria are capable of using other atoms than oxygen to act as the terminal electron acceptor.  When UV light is also absent simultaneously this increases their ability to grow in a woman’s skin even more. UV light is bactericidal. This causes a large increase in the phenol content of the skin/cornea because these bacteria are growing. Bacterial growth is linked to a lack of UV light exposure. 

In fact, bacteria contain substantial amounts of photo-sensitive amino acids compared to our cells. They have a lot of phenylalanine and tyrosine and those two amino acids are relatively rare in eukaryotic skin cell proteins by design. The reason for the bactericidal effect of UV light upon them is that they absorb greater amounts of UV light and they have no protective mechanisms.   It should now make sense to you why tyrosinase activity and the darkening of skin are linked. Tyrosinase is an oxidase (enzyme) that is the rate-limiting enzyme for controlling the production of melanin in our skin melanosomes. So decreasing tyrosinase activity WITH SUNSCREEN darkens the skin.

14. Taking exogenous melatonin orally is equivalent to using sunscreen.  Why?

Taking melatonin orally chronically without blocking blue light can lead to serious eye damage. Here are two eye-opening papers on why you better make sure you have the right people packing your parachute.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2785757/

All oral doses produce the same response: they thin your retina by ruining photoreceptor regeneration. Whatever supplement maker tells you to take it does not know the data. If your cells and body make it endogenously, you’re not designed to take it exogenously. It is a simple rule of Nature.

 http://www.iovs.org/content/33/6/1894

15.  Using sunscreen will reduce your mood and if you do it long enough you will get various mental diseases.  Do it longer and you may become a suicide statistic.  Seasonal changes in sun time were found to best account for relationships between weather variables and variability in mental health distress. Increased mental health distress was found during periods of reduced sun time hours. A separate analysis examining subjects’ endorsement of a suicidality item, though not statistically significant, demonstrated a similar pattern. Initial results showed a relationship between pollution and changes in mental health distress; however, this was mediated by sun time.  We’ve known this for a long time in medicine, but you’d never know it from the advice given in the Dermatology and Ophthalmology clinics in the USA.

https://journals.sagepub.com/doi/pdf/10.1177/003591572902200434

16.  I almost hate to say this in this blog but I am compelled to.  Low-dose methylene blue use is a way to counterbalance chronic suncream abuse, blue light, toxicity, and the implantation of intraocular lenses.  I will not go into the mechanisms but if you are a physician and you understand the top 13 points you will see why this makes sense.  For the lay public, I do not practice medicine on these Patreon blogs and I will say this is why you want to hire decentralized MDs to advise you when you have some of these conditions.  Do not ask for the dose or how I do it because the answers will not show up magically in the comments below.  I used this strategy with a famous patient of mine and once he reveals the story fully online this topic is sure to make some waves on social media.  I expect that to happen in the first week of March 2023.

17.  If you use sunscreen or eyeglasses you might be more prone to addictions.  Why?  Addictions are associated with lowered dopamine states.  Dopamine is created via melanin biology.  Sunscreens block melanin production.

If migraines are linked to artificial light via the hypothalamus via POMC, and POMC creates our natural opioid beta-endorphin, is it possible drug addiction is somehow related to modern man’s abuse of man-made light day and night?

If we put a rat in a cage and give it 2 water bottles. One is just water and one is water laced with heroin or cocaine. The rat will almost always prefer the drugged water and almost always kill itself in a couple of weeks. That is our current theory of addiction. Is it right? Might a tighter connection with our environment that leads to entanglement or connection be the missing piece to the addiction equation? Is this radical thinking?

A wise researcher came along in the ’70s and said, “Well, hang on. We’re putting the rat in an empty cage under artificial light. It has nothing to do and it is doing it in bad light. Let’s try this a bit differently.” So the wise-built Rat Park and Rat Park are like heaven for rats. Everything a rat could want is in Rat Park. Lovely food. Lots of sex. Lots of darkness because rats are NOCTURNAL. Other rats were present to befriend. Colored balls. Plus both water bottles, one with water and one with drugged water. But here’s what’s fascinating: In Rat Park, they didn’t like the drugged water any longer. In fact, They hardly used it. None of them overdosed in this experiment. None of them use drugs in a way that looks like compulsion or addiction. What did the wise show? They showed that both the right-wing and left-wing theories of addiction are wrong. The right-wing theory is that it’s a moral failing, you’re a hedonist, and you party too hard. The left-wing theory is that it takes you over, and your brain is hijacked. It turns out the connection or lack of connection to our native environment is the missing piece to addiction. The wise say it’s not your morality, it’s not your brain; it’s the cage that becomes your prison that is the key to why you are addicted to something. Addiction is largely an adaptation to your environment due to a lack of entanglement or connection. This leads to a desynchrony of how things operate in your cells and this changes your behavior = see Prince, Lead singers of Soundgarden and Linkin Park.

Now, we created a society where significant numbers of us can’t bear to be present in our lives without being on something, drinking, drugs, sex, shopping… We’ve created a hyperconsumerist, hyper-individualist, isolated world that is, for many of us, more like the first cage than the bonded, connected cages we need.

The opposite of addiction is not sobriety. The opposite of addiction is connection or entanglement to Nature. And our whole society, the engine of it, is geared toward making us connect with things, not people. You are not a good consumer citizen if you spend your time bonding with the people around you and not stuff. In fact, we are trained from a young age to focus our hopes, dreams, and ambitions on things to buy and consume. Drug addiction is a subset to living a life without proper entanglement in Nature with the sun.

https://www.linkedin.com/pulse/time-rethink-your-truth-sun-jack-kruse/

18.  Why can’t young people sleep anymore?  Well, their parents have put sunscreen on them all their lives and this has atrophied their skin and eyes.  This means they cannot handle being out in the sun very long.  When I hear people tell me they are photosensitive I know how this was caused.  They are always in disbelief because of what they have been told by centralized nonsense.  Sunscreen, sunglasses, and modern tech screens while living indoors for their entire life.  They have no melanin.  They are manufactured albinos.

Blue light/nnEMF dehydrates cells because they stop H2O production from the mitochondrial TCA cycle.  Why is this a big deal? Neurons absorb and release water when firing information.  When H2O is missing in action in your cells so are neurological functions/capabilities.  You lose the ability to sleep and account for time in your molecular clocks when water is absent.  This is why all neurodegenerative conditions are exploding globally.

This is also why children experience time differently than adults.  Less water, less sunlight, or more ALAN at night destroy the clock-timing mechanism of living things.  Few see this recipe in life’s blueprint  The inability to sleep = lowered mitochondrial melatonin production = low NAD+ regeneration.  

https://www.nih.gov/news-events/news-releases/neurons-absorb-release-water-when-firing-nih-study-suggests

19.  Bone/Joint failure is made worse by sunscreen and sunglasses. Now you know why orthopedic surgeons are so busy replacing knees and hips over the last 100 years. This includes osteoarthritis, autoimmune arthritis, osteopenia, and osteoporosis.  Why?  Because blue light ruins POMC in the musculoskeletal system too.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410228/

20. Sunscreen creates huge profits for functional medicine practitioners who are ignorant about light.  How?  Sunscreen ruins H+ movements (light hydrogen) and when H+ movements are disrupted SNP’s/SAPs do not operate they way they should?  Why?  They both operate using proton tunneling.  In fact, all enzymes use proton tunneling to work. If you block sunlight with sunscreens and sunglasses you are effectiving enzyme kinetics.

D+= deuterium or heavy hydrogen.

SNPs expression is amplified when there is too much D+ to H+ in the mitochondrion of a cell – because the Enzyme kinetics is even more altered.

COX2 amplification occurs in mitochondria (light stress) = more D+ coming into the cell from COX2 action on PUFAs on the cell membrane (Deuterium webinars I did for my members).

This is why SNP issues weren’t really a problem 50-70 years ago with incandescent lights + quite a shitty diet + limited dirty electricity/ RF.  Those lights had some UV and red in them.  Modern lights DO NOT!!!!!

And this explains why functional medicine doctors are robbing people blind by treating their bad SNPs/SAPs on 23andme testing:  It also explains why they’re exploding now in the modern world cause it’s LED Lights + generally a good diet (sugar consumption has dropped) + huge D.E / RF

= Diet doesn’t affect SNPs… Deuterium fractionations do!!!

COX2 is how D+ is getting through and clogging up the TCA cycle in the mitochondrial matrix.

Structured Water and Charge (Sun) is how we limit the inflow of deuterium and keep it filled with H+.

Limiting D+ in diet (Keto/Carnivore/Boros/crooks) is a short-term remedy for SNPs/SAP issues but doesn’t solve the problem long-term until you understand the light story.

SUMMARY

The medium is the message.  Dermatology and Ophthalmology are the “mediums” Big Pharma has used to get you to believe the sun is toxic.  Today modern man does not live in sunlight.  So how could the sun be toxic?  Might it be the light we live under be the real problem?

If you are a physician and don’t realize our profession is dying on its own vine, you haven’t been paying attention to the science I am showing you daily.  Sunscreen supports centralized healthcare overuse = highly profitable for healthcare corporations.

What is the difference between a decentralized vs centralized MD?  Centralized MDs are told by their bosses to just treat the symptom of things and not reach for the cause.

There are a lot more links to how sunscreen can harm you but the list above is instructive and should shed light on why you need to avoid conventional advice about blocking the sun with sunscreen or sunglasses.  I hope you educate the ignorant around you with this mitochondriac wisdom.

This truth is discoverable, but the facts will be so dishonestly set forth in almost any media outlet by the “mediums” that the public can be forgiven either for swallowing lies or failing to form an opinion.  The reason for this is how the news is being delivered today about the sun.  The products of modern science and technology are not in themselves good or bad; it is the way they are used that determines their value to us.  Right now they are destroying the public’s health.

The difference between you and the “mediums’ today is education.  The profiteers got wiser and put the “mediums” on the media platforms to deliver their propaganda to change your beliefs to get you to stay out of the sun.  This began with Coco Chanel.  The actions of the mediums and media have resulted in “a public” that is too ignorant to explain why they’re experts are right or wrong on medical topics (think COVID/SUN), while the media is so smart they can collectively join forces online and make “wrong or bad medicine” sound good to most of the public.  The medium was designed to dull the senses and cognition of the viewing audience.  Lowered dopamine from a lack of sun creates compliant obedient idiots.  It has worked fabulously.  COVID uncovered their plan.  This is why Fauci wanted you out of the sun in lockdown and it is why the vaccine king, Bill Gates, wants to block the sun.  Your use of sunscreen and sunglasses make his agenda easier to obtain.

The public is now a product of the media and not their customer.  Advertisers are their chief customers = Big Pharma.  Public viewers are now quite cheap because of how the news is delivered in the technocracy.  When viewers realized they have been made a cheap commodity, they can easily force the cost of their services higher to cause the financial collapse of the media.

Why should you care?  Once we have surrendered our senses and nervous systems to the private manipulation of those mediums paid by Big Pharma to work the airwaves in the media who would try to benefit from taking a lease on our eyes and ears and nerves, we don’t really have any rights left.

If Covid has taught you anything don’t discount what initially appears as nonsense. The most fatal illusion is the settled point of view. Nonsense is nonsense only because we have not yet found that point of view from which it makes sense to us.  A fixed point of view in life usually harms anybody who has one.  Nature’s knowledge is never final.  There are no axiomatic truths in medicine or science.  This is why the scientific method exists.  To continually test what we know for new data.  Wisdom tells me what is correct today, is likely going to be wrong in the future.

If you want to be the most innovative person in your space – get outside of it, regularly. Sunburns like the one I got above is not a death sentence.  In fact new data show the opposite.  (see below)

Conversations with people doing the same job you do can expand your box but rarely pushes outside of it.  Go to spaces no one else cares about and you’ll end up dominating your own.

^^^^^You live longer when you are in the sun.  Sunscreens keep you out of it.

The education system today feeds the government narrative to create obedient idiots. This preconditions the human brain for future planned events to support the paradigm in power.  

Sunscreen & sunglasses helps them and hurts you.  

CITES

https://onlinelibrary.wiley.com/doi/full/10.1111/exd.12715

“Writing in a report summary in 1979, John Calhoun noted that “no single area of intellectual effort can exert a greater influence on human welfare than that contributing to better design of the built environment.”

June 22, 1972. John Calhoun stood over the abandoned husk of what had once been a thriving metropolis of thousands. Now, the population had dwindled to just 122, and soon, even these inhabitants would be dead.

Calhoun wasn’t the survivor of a natural disaster or nuclear meltdown; rather, he was a researcher at the National Institute of Mental Health conducting an experiment into the effects of overcrowding on mouse behavior. The results laid bare at his feet, had taken years to play out.

In 1968, Calhoun started the experiment by introducing four mouse couples into a specially designed pen—a veritable rodent Garden of Eden—with numerous “apartments,” abundant nesting supplies, and unlimited food and water. The only scarce resource in this microcosm was physical space, and Calhoun suspected that it was only a matter of time before this caused trouble in paradise.

Calhoun had been running similar experiments with rodents for decades but had always had to end them prematurely, ironically because of laboratory space constraints, says Edmund Ramsden, a science historian at the Queen Mary University of London. This iteration, dubbed Universe 25, was the first crowding experiment he ran to completion.

IS THERE A HUMAN CORRELATION TO THIS EXPERIMENT ON GOING ON NOW?

What happens over a few generations when they give up on having sex?  Well, female children will experience follicle failure and male children experience low sperm counts.  There is no reason to have sex when you’re infertile and today most of the world is headed this way.  How will it end for humans?  The same way it did for the dinosaurs when something from the environment changed the light on the planet.  EXTINCTION.

What causes celibacy syndrome in Asians who make made love to the 5 G devices on Wifi with no blue blockers on?  Myopia, low dopamine, and a sexless life begin as deuterium fills their mitochondrial matrices in all the various tissues in their body.

As dopamine drops many things happen but the most consequential thing that occurs is that you lose your ability to perceive time properly.

I’ve written extensively about the “celibacy syndrome” in Asia that is developing in young people in the Ubiquitination series of blogs. Many people did not see the link to nnEMF and how it causes massive assimilation of MASS into the mitochondrial matrix to cause many collateral problems in cells. Now we have more data showing us what happens when we allow blue light and nnEMF to destroy how our endocrine system works with light from the sun via our eyes and skin.  This is what the implication of my Vermont 2017 talk on youtube was all about.

How many of you “naked apes” out there get the implications???   How should we supplement to fix this deuterium mass problem? Do like the Sphinx does every AM. Look toward sunrises while grounded to become moist supple and sexy….. you should make an effort to look in the direction of the sun…….not directly at it………from sunrise til 9-10 AM. Most cannot do this because of modern life. Their lives keep them from it, so they lose dopamine and melatonin as deuterium rises in our mitochondria and wonder why they cannot turn on or off the compound pharmacy in their brain. Their beliefs around light use are why this happens.

Beliefs block us from atomic recycling that light controls. We are all recycled atoms at our fundamental basis that are altered by the light that hits us to get the life we get.

Sunlight creates dopamine and dopamine is the guardian of your pituitary gland and this is where sexy time begins. Without sexual activity in young people,  extinction is on the human agenda over the next few decades.  Leptin is the hormone that controls fecundity but many have forgotten that link to light.

In the last two years in cities, longevity has declined for the FIRST TIME in human history.  Regarding sex, dopamine controls what the endocrine system can or cannot release hormones to cells in your body and this zaps your libido and performance. As light energy changes via your eye dopamine levels alter in your eye. This changes the world you receive and understand. As energy slows down for any reason, it changes its form and becomes matter, the substances we think we know best in our world. The problem is we are fooled by what we think we now know because we have no idea what we are missing. This is the modern world’s Dunning Kruger moment. Science is ever-changing and incomplete, but it always maintains its own resistance to new and better ideas.

Today, metaphors reign large in biochemistry, where quantum mysteries reside below the surface ready to take out the “smart naked apes” just as she took out the T-Rex. Those mysteries are where all of our truth lies. A lowered dopamine is what creates this false reality today.  Lowered dopamine creates the illusion that we have more time than we really do.

Those who think that the loss of libido (the natural desire for sex) is something that only happens to people of more advanced age, today you’d be seriously wrong.  Alien light can do it and has been doing it for some time.  Before extinction, manifests diseases in the young that used to be rare will become common.  Myopia, autism, autoimmunity, obesity, T2D, AMD, and cancer are a few.

Both men and women in their late twenties are reporting a lack of interest in their own sexuality to their doctor or therapist, and even younger people are wondering where their desire for sex has gone.  Thank Apple, Facebook, Cisco, and Google.  their blue light and alien nnEMF networks were built to sell you virtual sex lives online and none of you intelligent naked apes saw it coming.

MODERN REALITY

THE CALHOUN EXPERIMENTS WERE EYE-OPENING THEN, BUT PEOPLE STILL DO NOT UNDERSTAND WHAT THE EXPERIMENTS RELAYED TO US.

“The “Universe 25″ experiment is one of the most terrifying experiments in the history of science, which, through the behavior of a colony of mice, is an attempt by scientists to explain human societies. The idea of ​​”Universe 25” Came from the American scientist John Calhoun, who created an “ideal world” in which hundreds of mice would live and reproduce. More specifically, Calhoun built the so-called “Paradise of Mice”, a specially designed space where rodents had an abundance of food and water and a large living space.

The living space, however, was in a laboratory that had modern man’s light exposing it while the experiment was ongoing.

In the beginning, he placed four pairs of mice that in a short time began to reproduce, resulting in their population growing rapidly. However, after 315 days their reproduction began to decrease significantly. When the number of rodents reached 600, a hierarchy was formed between them and then the so-called “wretches” appeared. The larger rodents began to attack the group, with the result that many males begin to “collapse” psychologically. As a result, the females did not protect themselves and in turn, became aggressive toward their young. As time went on, the females showed more and more aggressive behavior, isolation elements, and lack of reproductive mood. There was a low birth rate and, at the same time, an increase in mortality in younger rodents. Then, a new class of male rodents appeared, the so-called “beautiful mice”. They refused to mate with the females or to “fight” for their space. All they cared about was food and sleep. At one point, “beautiful males” and “isolated females” made up the majority of the population.

According to Calhoun, the death phase consisted of two stages: the “first death” and “second death.” The former was characterized by the loss of purpose in life beyond mere existence — no desire to mate, raise young, or establish a role within society. As time went on, juvenile mortality reached 100% and reproduction reached zero. Among the endangered mice, homosexuality was observed and, at the same time, cannibalism increased, despite the fact that there was plenty of food. Two years after the start of the experiment, the last baby of the colony was born. By 1973, he had killed the last mouse in the Universe 25. John Calhoun repeated the same experiment 25 more times, and each time the result was the same.  Each time there were no light controls.

Modern life also has no life controls.  Stop and think about your world now.

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Calhoun’s scientific work has been used as a model for interpreting social collapse, and his research serves as a focal point for the study of urban sociology.

Sadly most people carefully read the paper’s methodologies to realize that mice are not adapted to living in a lab indoors disconnected from their natural habitat and light source.

UNIVERSE 25 picture above: John Calhoun crouches within his rodent utopia-turned-dystopia that, at its peak, housed approximately 2,200 mice. Calhoun studied the breakdown of social bonds that occurs under extreme overcrowding, a phenomenon he termed a “behavioral sink.”  YOICHI R. OKAMOTO, WHITE HOUSE PHOTOGRAPHER, PUBLIC DOMAIN

We are currently witnessing direct parallels in today’s society; weak, feminized men with little to no skills and no protection instincts, and overly agitated and aggressive females with no maternal instincts. I wonder when people will control for light in all experiments.

Calhoun’s experiments showed us the effect of incandescent light on nocturnal mammals.  Can you imagine what the effects of these types of experiments are when you add in 5G and all the other parts of the electromagnetic spectrum outside the visible spectrum?

Sunlight is the foundation layer of Nature that gives rise to everything else.

Manmade light is not foundational to Nature and it induces collateral biological effects

Therefore, when sunlight breaks down because of modern life and centralized healthcare beliefs, standing your ground when the ground gives way will provide little in the way of safety.

How is sunlight breaking down and what should we look for as evidence of the failure?

Central healthcare is manipulating the narratives around sunlight at an unprecedented rate to avoid a profit collapse of the system they’ve built over the last 100 years.

Using information theory as a beacon it follows that misinformation around sunlight MUST be growing throughout the system if you look for it.

I write about that evidence every day and few people value it.  If they did more people would be reading my work on Patreon.

It follows as a second-order derivative of that misinformation is that trust MUST be declining throughout the healthcare system.  We have seen that in the government and economy for the last few years.  We’ve seen that in biology of diseases which have exploded over 100 years.  Not everyone realizes that what has gone on with COVID is linked to the misinformation about sunlight.

Because physicians/patients measure a system from within the system, for most of the population, it would make the truth virtually impossible to see.

With this misinformation as a backdrop and a new protocol layer technology emerging (decentralized mitochondrial medicine).  You must remember that open protocols provide the most value to society and are the hardest to understand it would be extraordinarily difficult to see why mitochondrial medicine alone stands out as a breakthrough technology and where it is heading.  You as a patron are part of that movement toward truth.

By extension, it would be relatively easy in this environment for ill-informed or bad actors to conflate sunlight with manmade light, WiFi, LiFi, nnEMF, cosmic radiation, and other “light conventions” to gain an advantage for their offering.

SUNlight is information.  It is the most critical information for you to get right now

CITES

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1644264/

A cardiac arrest is an acute loss of electric power to the heart.  When the heart fails rapidly what do we do?  We re-shock it to get it started.  The electrical shock restores the decentralized networks in us.  This is why adenosine is part of the ACLS protocol with AED therapy.

IS INTENSE RED LIGHT CAPABLE OF REPLACING AN ACLS DRUG?

SVT is a broad term for a number of tachyarrhythmias that originate above the ventricular electrical conduction system (Purkinje fibers). In cardiac arrest algorithms, ACLS tells us to use adenosine via IV push to rid the heart of this detrimental rhythm until the patient is not symptomatic.  Why adenosine?

Did you know red light from the sun creates adenosine normally in the heart when it is exposed to sunlight?

Modern humans rarely expose their skin to sunlight and this is one reason cardiac death is a leading cause of death in humans.

IS THERE NOW EVIDENCE THAT INTENSE RED LIGHT can do THE same thing using the PER circadian gene system? Does this imply that red light is a drug equivalent?

YES.

Is there more to this circadian story you need to know? YES.

Adenosine-mediated increase of cyclic AMP (cAMP) is a core component of PER2 expression and PER2-mediated ischemic preconditioning of the heart.  This means sunlight creates a perfect circadian situation for oxygen in the heart and its conduction system.

THE KEY HISTORY LESSON

The most dramatic event in the history of the earth was the arrival of sunlight and its effect on oxygen on Earth due to photosynthesis.  Sunlight caused the great oxygen event. With sunlight, trillions of photosynthetic algae could now make oxygen, transforming the entire planet’s atmosphere and setting up the perfect storm for the evolution of a mammalian mitochondrial world.

This study on adenosine, red light, and the heart shows, on a molecular level, that intensive red light therapy offers a better strategy for treating or preventing low oxygen conditions like myocardial ischemia.  Why?  Red light has no side effects but all drugs do.

In this paper below in an effort to find out why red intense light can do this, researchers developed a photonic strategy using optogenetics to protect the heart using intense light to target and manipulate the function of the PER2 gene which is expressed in a circadian pattern in the part of the brain that controls circadian rhythms. (Sounds like something Dr. Kruse would suggest no?)

You do know that sunlight is made of 42% intense IR-A light huh?

By amplifying this gene, the researchers using JUST LIGHT PHOTONS, found that it protected cardiovascular tissues against LOW OXYGEN conditions like myocardial ischemia, caused by reduced oxygen flow to the heart. Dr. Kruse called low oxygen situations pseudohypoxia. These are all associated with low NAD+ levels in cytochrome 1 and leptin resistance with low delta psi on the inner mitochondrial membrane.

They also discovered that bright light increased cardiac ADENOSINE, a chemical that plays a role in blood flow regulation and sleeps. Hey didn’t Dr. Kruse just do a massive post on ADENOSINE last week on his FB page?  Yep.

Mitophagy contributes to mitochondrial quality control not only by removing damaged mitochondria but also by promoting the biosynthesis of new mitochondria. It has been demonstrated that there is a crosstalk between the mitophagy pathway and the mitochondrial biosynthetic pathway (10). Specifically, Plaikaras et al. established that mitophagy and mitochondrial biosynthesis are interfaced with each other to maintain mitochondrial homeostasis.

The implication of this work is there’s no need to take PQQ, and other supplements, if your sleep is sub-par. Sleep and sunlight remain king and queen.  Sunlight controls the adenosine levels in humans

Hey, isn’t leptin resistance a synonym for melanopsin dysfunction? Yes, it is. Tell me again how that works Dr. Kruse.

My Response: Blue light and nnEMF liberate Vitamin A from our cells and cell membranes to raise its presence in the blood plasma and this lowers plasma levels of Vitamin C and Vitamin D. When Vitamin is liberated by non-terrestrial light or trauma, it becomes an aldehyde that destroys the small molecule modulators of the mammalian circadian mechanism. PER1 and PER2 are light gears in that eye clock mechanism.

It raises the question what in the hell do PER genes do?

Cell hypoxia is controlled by the hypoxia-inducible factor (HIF-1).
Do you know the link between HIF 1 to sunlight and oxygen?  Light and oxygen-sensing pathways are linked on a cellular level in ALL mammals (Gu et al., 2000, Hogenesch et al.,1998, McIntosh et al., 2010).  Hypoxia-inducible factor 1⍺ (HIF1A), is an evolutionarily conserved transcription factor enabling cellular adaptation to low oxygen availability (Semenza, 2011).  Here is the kicker:  It belongs to the same protein family as the light-inducible circadian core protein Period 2 (PER2) (Liu et al., 2012).

HIF-1 is what the entire hypoxia series was about on Patreon.  Review those blogs sometime.

So when you’re missing sun your cells sense your missing oxygen and HIF-1 goes up and PER circadian mechanism genes go awry.  The circadian mechanism loses its periodicity.  Remember what you learned on Patreon about periodicity?  Periodicity is a synonym for the circadian clock mechanism.  This ruins every cycle in the cell that relies on it.  

Once the molecular clock in the eye and peripheral clocks goes awry the implications for many neolithic diseases spiral out of control. What are some of the Vitamin A proteins involved in this downward spiral?

They are called retinoic acid receptor-related orphan nuclear receptors or RORs for short. The RORs have several isoforms too called RORα-γ. These proteins are also under the transcriptional control of CLOCK/BMAL1 heterodimers.

CLOCK and BMAL1 are positive regulators of circadian gene expression, and PER and CRY are the NEGATIVE FEEDBACK LOOP regulators that operate under day and night cycles. These are the positive and negative feedback arms of the circadian mechanism.

They must be coupled properly to terrestrial light to operate well and control all growth and metabolism, protein synthesis, and hormone production and release. It also controls receptor biology. It controls EVERYTHING. If they are not properly coupled to the light and dark cycles the eventual results are the extinction of both sides of the feedback loop. So when sunlight is absent we lose control of the negative feedback loop of the circadian mechanism controlled by PER2.  This is what causes the NAD+ drop in mtDNA.  That is how all human disease begins. It is circadian biology that couples all the molecular clock genes in humans and the SCN of the eye drives the program and the major timekeeper.  The SCN as the metronome of biology loses accuracy as PER2 drops.  PER2 is critical in controlling the optical periodicity of the circadian mechanism.

Are heart rhythms are controlled by the circadian mechanism in humans?

Yes, they are.  The enzymatic flux of the entire TCA cycle is also controlled by it in the electrical system of the heart.  Cardiac arrhythmias are a leading cause of cardiovascular death in humans. It has long been accepted that life-threatening cardiac arrhythmias (ventricular tachycardia, ventricular fibrillation, and sudden cardiac death) are more likely to occur in the morning after waking. It is perhaps less well recognized that there is a circadian rhythm in cardiac pacemaking and other electrophysiological properties of the heart. In addition, there is a circadian rhythm in other arrhythmias, for example, bradyarrhythmias and supraventricular arrhythmias.

Two mechanisms underlie this finding:

(1) a central circadian clock in the suprachiasmatic nucleus in the hypothalamus may directly affect the electrophysiology of the heart and arrhythmogenesis via various neurohumoral factors, particularly the autonomic nervous system; or

(2) a local circadian clock in the heart itself (albeit under the control of the central clock) may drive a circadian rhythm in the expression of ion channels in the heart, which in turn varies arrhythmic substrate.

Remember the free decentralized lesson from my FaceBook page on 7/31/2019:

I said, “Classic Paroxysmal SVT (supraventricular tachycardia) has a narrow QRS complex & has a very regular rhythm. … A rapid heart rate will significantly reduce the time which the ventricles have to fill.

The heart fills during diastole, and diastole is normally 2/3 the cardiac cycle. A rapid heart rate will significantly reduce the time that the ventricles have to fill. The reduced filling time results in a smaller amount of blood ejected from the heart during systole. The end result is a drop in cardiac output & hypotension.
With the drop in cardiac output, a patient may experience the following symptoms.

These symptoms occur more frequently with a heart rate >150 beats per minute as the ECG strip shows below:
Shortness of air (S)
Palpitation feeling in the chest (S)
Ongoing chest pain (U)
Dizziness (S)
Rapid breathing (S)
Loss of consciousness (U)
Numbness of body parts (S)

The pathway of choice for SVT in the tachycardia algorithm is based on whether the patient is stable or unstable clinically.
The symptoms listed above that would indicate the patient is unstable are noted with the letter (U) in a cardiac code situation. This can present outside a code situation when someone has a very low redox state because of a very poor environment linked to blue light and nnEMF toxicity. This mimics adrenal fatigue and brainstem pathology, sleep disorders, and eating disorders. Stable but serious symptoms are indicated with the letter (S) above.
Insert any 3G-5G city or environment. a \/, trauma, poor sleep = an acute or chronic adenosine problem.

HYPERLINK

What screws up sleep ultimately in decentralized networks in cells? Problems with adenosine at the brain stem level. Go look up what adenosine signals in us.  It is the biochemical signal that begins the sleep cycle in humans.  This is why ACLS uses adenosine to treat acute mitochondrial failure in the heart that results in SVT cardiac rhythms……..guess what drug is used for cardiac tachycardias in ACLS?
ADENOSINE via IV push = a DEFECT IN PER 1 or PER2. SOUND FAMILIAR?

Light-deficient humans get electrical problems in their hearts before the disease begins that people can see and sense.  That is what bad rhythms mean in patients whose heart is still pumping but acting badly.  They are all light deficient, solar light deficient, and most of the time blue light toxic. 

How do you like me now?

When the system teaches ATLS/ACLS/BLS/CPR recertification you can see where their focus really lies if you are paying attention. Pre-covid videos and protocols are available for you to review. Every variable has been subjected to intensive statistical analysis to increase the odds of survival, but there will be no mention of how a broken circadian mechanism leads to all codes covered by their protocols.  That includes myocardial infarction, clots, or seizures; which are the most common cause of acute arrest today.  To a decentralized mindset, you might think this omission of the circadian defect should invalidate the stats and protocols they regurgitate until you realize what perspective they play this game with.

For example, historically, a small child has been more likely to choke or ingest a poison than suffer spontaneous heart problems than an older child or adult. The protocols never take new data that the system is built around.  This eliminates new decentralized options and just keeps publishing ideas of treatment that are based on data that may have changed and has not been updated. No updates or changes for first responders are present, except for the new advice of not performing mouth-to-mouth resuscitation on kids. I wonder if we will ever acknowledge the elephant in the room, and change our dataset and actions or if organizations like the AHA, ADA, FDA, CDC, and USDA will continue to feed us garbage into perpetuity.

Why would you expect a centralized healthcare Rx to be set up to work for you based on their perspective on health?   Do you realize who is being harvested and bled dry by these beliefs??  The public is.  If you knew the sun fixes this and drugs induce many more problems than they solve you’d realize you really do not need most of what centralized healthcare sells you.

How does a centralized healthcare system operate?  Is it for your benefit or theirs?  In most cases, protocols are set up for the chronic profiteering of the system.

Centralized healthcare remains fully ignorant about how light operates in our bodies by design. The people who profit make the curriculum that the experts are forced to learn from organizations like the AHA, ADA, FDA, CDC, and USD so they can sell products, drugs, foods, and suncream to you because their advice is given to you when you visit the centralized system for advice. It is a giant financial feedback loop and you are the patsy. The decentralized healthcare system warns you with data (adenosine a drug in ACLS can be replaced by the red light of the sun to get the same effect for the heart)  that if you avoid the sun and wear suncreams the guys selling as the centralized solutions (Pharma/food/AHA/CDC/FDA facade) their profits rise while your health risks multiply over time. As the risks rise they are ready to wallet biopsy you as an inpatient next. The centralized circle of life explained.

I’m shocked you’re shocked.

IS THIS ALL HYPERBOLIC TALK?

Does centralized medicine have direct evidence that is visual that we are built entirely from many decentralized networks?

What can lightning strikes of living systems teach us about life?

Lichtenberg figures are reddish, fern-like patterns that appear on the skin when a patient is struck by lightning. These appear to be a result of an inflammatory response to the electric voltage as the current spreads out causing ionization and heat effects and damage to the small subcutaneous capillaries.

It tells us more about us and less about light. We are photoelectric beings and the marks on us outline many of the decentralized networks operating inside our cells. https://www.frontiersin.org/articles/10.3389/fmed.2021.663807/full

SUMMARY

The fastest way to make Lichtenstein’s marks vanish is to add red light back to the system.  It sounds a lot like how we make SVT vanish from heart rhythms, doesn’t it?  This makes electrical sense when you understand what these ferning patterns are on the skin.  They are a sign of an electrical discharge in the body that has lost an acute amount of redox power.  Red light is the easiest way to recharge the body quickly so its addition to the skin will make the repair happen more rapidly.

As cite one below shows us, the new mRNA \/’s can cause sudden cardiac arrest and we had visual evidence of that recently in an NFL game.  Many of you will read this and not believe it.  I want to remind the skeptics of this reality that also occurred this year in NFL circles.  Remember when JJ Watt had to have his SVT treated after he was injected with mRNA technology?  What did they do to treat him?

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They had to emergently shock his heart back into a sinus rhythm because the drugs they gave did not work.  This is really bad news for anyone who took the government mandate seriously and complied with it.   Do you think this might have anything to do with why he is retiring from the NFL now a few weeks later?  I think Demar Hamlin’s acute cardiac arrest on MNF in front of the US public is going to become a commonplace post-vaccine mandate.  JJ Watt’s case tells us that you do not need trauma to induce an arrest.  A bad rhythm may come first before the arrest occurs.

Might the same prescription of using light to combat disease be important in helping someone overcome that centralized healthcare injury?  Does this Tweet video look normal to you?

TWEET

Mitochondriacs know that answer.

Do you?

CITES

https://twitter.com/vascohill/status/1613610308140138496

https://twitter.com/P_McCulloughMD/status/1613685112033394689

https://academic.oup.com/ehjcr/article/5/3/ytab054/6154461

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520649/

https://nigms.nih.gov/education/fact-sheets/Pages/circadian-rhythms.aspx

https://geardiary.com/2011/06/17/meet-winston-kemp-lightning-strike-survivor-and-lichtenberg-figure-owner/

https://www.cell.com/cell/fulltext/S0092-8674(13)01521-3