The retina and anus do not get supplied Oxygen from the cardiac system. The components of the anus are drastically reduced chemically and adding oxygen will do very little so nature looks to conserve energy at all cost and the ideal to supply the whole body with blood and Oxygen is sacrificed.
The eye is the most chemically active site in the body because of the light it interacts with and the light it makes. The entire surface of the eye is directly exposed to the oxygen in atmospheric air volumes. It has no blood vessels in the cornea and fovea BY DESIGN for some reason. It also uses a Warburg metabolism for SOME reason. Siegfried calls this metabolism pathologic and he is DEAD WRONG to misinform the public.
The gadgetry of the eye operates photochemically 100% of the time. It’s through this process of absorption of photon that your eyeball receives much needed oxygen. 1- outer surface directly exposed to air 2- photo transducers buried within 3- photon bombardment
Without those three the eye is hypoxic = pseudohypoxia leads to disease = low NAD+ - Starved of Oxygen = change in ROS/RNS = change in biophoton spectra of the cell. This will cause a slowing down of the signal to the hypothalamus. This downregulates hormone production and metabolism for the whole body. This is where hormone changes begin.
The circadian rhythm is set by the eye being the fastest clock. If you slow down the calibrating clock, you slow down every clock. Your circadian rhythm is misaligned and your metabolism and hormone production suffers.
Caused by glasses
Caused by sunglasses
Causes by contacts & refractive surgery
Caused by all sunscreens
Caused by clothing
Caused by indoor air
Caused by living behind glass doors/windows
Caused by polluted air
Caused by geoengineering
When we go up in elevation, O2 in the air decreases and we can experience shortness of breath. The functioning of the eye is protected in this instance.
So how would going up in elevation be different from glasses,indoor air,pollution? All reduce oxygen. What’s the difference?
MORE UV at elevation
Less UV in pollution
No UV inside or under magnification lenses. The UV increases the photochemical properties of the eye gadgetry to make up the difference. Those other scenarios see the noose tightening for the entropy of the eye.
The SCN eye clock is really the metronome of the body. Circadian rhythmic cycles govern all biology and is proven by the period and timeless crystals produced by DNA.
One more thought provocation: When we sleep, our eyes remain shut. This would seem like contact lenses for oxygen at the corneal level of the eye.
When we sleep we reduce breathing and metabolic function body wide. Much less oxygen is needed. Also the UV plays a role in sleep. Our cells produce their own UV to regenerate and repair with the least amount of input from outside environment. So UV light makes up the difference from low O2, when we sleep or when we go up in elevation.
One more point: the water Nature make is deuterium depleted at elevation and this enhances energy transduction when compared to sea level. When we hydrate and eat locally, at elevation. It’s a coupled system that’s uncoupled by the modern standard of living. One that misses many clear points. jackkruse.com/ubiquitination…
2. LIGHT > FOOD at all levels.
CART (cocaine- and amphetamine-regulated transcript) peptides are neuromodulators that are involved in feeding, drug reward, stress, cardiovascular function, and bone remodeling. CART peptides are abundant but discretely distributed in the brain, pituitary and adrenal glands, pancreas, and gut. CART has a homeostatic function in the nucleus accumbens by blunting the effects of the drug-induced increase in dopamine release.
IMPLICATIONS?
CART peptides reduce the rewarding effects of cocaine and inhibits the context induced reinstatement of reward seeking.
Did you know that melanin and MCH reduce CART effects? Vitamin A levels in the blood and CSF tell us a lot about melanin biology inside the brain. Today's new blog tells us how Vitamin A tells this decentralized story. It is just another data point that shows light trumps food in control mechanisms in mammals.
3. Most people have no idea how the retina and brain get injured by technology. Fewer know there is injury current that stimulate them to regenerate. Fewer of them know that ferroptosis is how blue destroys the brain's non visual photoreceptive system. As a neurosurgeon most of the diseases I treat are related to ferroptosis signaling gone awry. This is why the daylight computer I had a hand in coming to market matters to humans with diseases of the neuroectoderm like brain tumors, autism, skin cancer, and AMD. Ferroptosis is critical in each disease in different ways.
The manner you use technology needs to change permanently.
Change can start with a single decision, action, or event, and its effects can ripple out in unexpected ways. It is often difficult for the centralized thinker with low agency to pinpoint exactly when or how change begins, as it is a complex and dynamic process influenced by a multitude of factors.
Similarly, the end of change is often ambiguous, as it can continue to evolve and adapt over time. Change is a constant in life, and it is important to embrace and navigate it with an open decentralized mindset while embracing a willingness to learn and grow. By being attentive to our surroundings and open to new experiences, we can better understand and appreciate the transformative power of change.
This NEW blog lays it all this science out. It updates the biophysics of where Dr. Robert O. Becker left off once the military ended his research career -----> patreon.com/posts/79959650
4. This blog has the key metric of why the eye, PVN, and DLF of the brain stem sleep and pain areas give the input into the cardiac and celiac plexus to cause rhythm and gut problems. Implications of this connection are massive in many other diseases besides bipolar disorder. Dopamine (from Tyr or melanin degradation) is made in the eye several ways by sunlight and it can be made in the gut by your microbiome due to the link to melanin. People forget that bacteria release 5000 times more light than eukaryotic cells and this light is capable of making dopamine from the aromatic amino acids in the gut. This is why serotonin and phenylalanine and tyrosine are stored in the enterochromaffin system there. The more and more you look into its biology, I feel more confident in saying that Light is the most powerful drug for living systems. The light release is more important than the fuel in the diet for our health outcomes because food has light information built into photosynthesis. This stimulus leads to light release to start the optical signal cascade in the gut using aromatic amino acids as the mover in the GI tract. When you are blue light/nnEMF toxic you cannot repair the gut or sleep issues at all. The same thing will be true for pain thresholds and opiate use. I can tell you this. Your gastrointestinal system will never function optimally in a circadian mismatch (melanopsin/encephalopsin dysfunction) and that will bypass however good a diet is. ----> patreon.com/posts/quantum-…
5. What is the biophysical evidence that supports why there is no optimal diet for any animal on Earth? Photosynthesis on land and sea is always in a constant state of flux due to movements in the and on the planet that animals are impotent to perceive. This is why the mitochondrial system is highly adaptabile to to latitude and longitude and incident light waves.
Our species often claims to hunger for truth, but seldom like the taste when it's served up. Humans are a plethora of stolen viruses and a depleted bacteria. Evolution creates each new species so that it carries with it a plethora of opportunities to make it in this brave new world. Man has pushed nature's limits because we are the only creature who refuses to be what we are. The Earth only plays music for those who listen to her tune. Those who don't listen are forced to changed or they become extinguished.
Below is 2 billion years in the evolution of the Earth, showing motion of the continents & circulation of the mantle. This remarkable simulation captures things humans cannot see, on timescales we cannot experience. The one thing that has captured this motion is cells. The organelle that proves this information has been captured by cells is a mitochondria. vimeo.com/194834420/desc…
6. Why are modern humans in deep shit? Blue light indoors causes ACTH and CLIP release in unison = high blood glucose and high insulin.
The food gurus want to keep selling you the idea that sugar and fructose appear to mimic disease because blue light and non-native EMF have become ubiquitous in the human environment for 150 years. This fallacy needs to die in decentralized healthcare, along with the use of modern lighting. Return to the sun and regain decentralized wisdom. We have to stop blaming sugar for what man made light is causing = TECHUFACTURED LIGHT is where chronic diseases begin.
In outdoor life seasonal change brought mammals cold temperatures. What did that do to POMC cleavage that differs from today's environment? When it is cold, and 380 nm light is ABSENT, insulin does not work as it does when the temperature is higher and 380 nm is present. Why? Because the biophysics of the non-visual photoreceptors in the skin change protein receptors in your cell membranes. As a result, your body changes as your physiology adapts. What is that non-visual photoreceptor called? Cholesterol. It changes the electric potential in mammalian membranes and this changes protein function while also altering voltage-gated channel operations changing the reality of the mammal as its environment varies.
Cholesterol is needed by the cell in many other zip codes where organelles live. When the system is under duress like it is with cold stress, blue light or nnEMF. To be used properly, cholesterol production is upregulated to stabilize membranes to change its electric potential to deal with varying light frequencies while still retaining the ability to make all our hormones. What really are hormones?
All hormones are light ferries (that break symmetry) from our skin delivering light to tissues and cells. This light is what fills the electronic level in us to create the dissipative state.
During my 18 months of unlearning to relearn, I found out that symmetry in crystals is key. When symmetry is broken by any phase transition in chemistry (water) energy and information transfers must occur by nature’s laws. This was how sunlight information and energy entered our bodies. I realized at that moment melanin, Vitamin D, T3, T4, RBCs, etc were all semiconductive crystals transferring data from the sun to our bodies.
That wasn't a lesson plan in medical school that was paid for by BigHarma's dollars. Mammals live longer because their mitochondria release heat to alter water chemistry they also make. That CO2 they make is big too because of the effect it has on magnetochemisty (ROS/RNS) in cells. Why? In cold temperature, mammals us their wide band gap semiconductors to create VUV-UV-A light endogenously to outperform and create massive amounts of light stronger than the environment provides.
Note it has zero to do with your gym work, breath work, or diet. But you're allowed to believe whatever lie you choose too.
📷
7. Why should you question the food gurus? How many of them have hacked the periodic table and can explain why this is critical to you? I finishing off my periodic table hack for you to review ======> completes the food and seed oil story forever.
Seed oils are a problem but not for the REASONS the smooth brainers think. (food gurus)
People who soar are those who refuse to sit back, sigh and wish things would change. They wander in nature’s decentralized networks. They neither complain of their lot nor passively dream of some distant ship coming in. They just live the life they create with the time and value they carry. Rather, they visualize in their minds that they are not quitters; they will not allow life’s circumstances to push them down and hold them under.
We are unaware that we live simultaneously in two worlds, with two realities: the inner city of our thoughts, emotions, and attitudes, and the outer reality of people, places, things, and events. Too many of us allow the outer world to dominate our sense of what is real. This causes our inner reality to react and not live. In this way, you never tap your full power as a person. Begin by disconnecting from the noise of the outer world and connecting to the silence within you. When you do this you can make sense of the disturbance going on around you.
Make your mental blueprint off your inner world, and begin to create. Nature = TIME + PLACE of atoms matter deeply.
8. I'm done toying with the shills in centralized science. You feel me yet?
What I have learned about Public Health over my surgical career? Talk is cheap for centralized politicians and epidemiologists.
Since talk is cheap, then being silent is expensive for the public and for MDs. Most folks it seems, can't afford to buy into it. It is wise to be aware of people who are standing in your midst and who refuse to smile when you win.
Make sure during this time you carefully reevaluate your own decentrlaized network of misfits.
Check out this article that teaches why UVa light and mTOR link: PUSHING A CANCELLED RESEARCHER TO THE FINISH LINE. linkedin.com/pulse/pushing-…
9. WHY FOOD DOES NOT MATTER: THE BIOPHYSICS ARGUMENT
Back at the origin of life 3.8 billion years ago on Earth electric membranes drove CO2 fixation by converting gases from volcanoes (driven by the solar plasma) into organic chemicals to create growth in the absence of oxygen. This was the first step life took at the ocean floors.
Metabolism has always been spontaneous on Earth. Today, we believe complex life emerged from ancient autotrophic pathways fueled by volcanic gases as carbon and the sun as ultimate energy sources. Variants of these pathways remain in modern autotrophs in the deepest branches of the tree of life. In this way, the DC electric current in membranes preceded all chemistry.
The energy metabolism of modern autotrophs resembles the geological interactions of H2 and CO2 gases in hydrothermal vents. Centralized science believes this points to a metabolic origin of biochemistry at the interface of the lithosphere and hydrosphere.
GENES only modify metabolism they do not control your life decisions or your outcomes. The light signals in your environment do that.
Decentralized science believes this points to a quantum thermodynamics at the core of life because the sun drives all these processes. This step is fundamentally why light tops food in all my discussions.
10. WHY FOOD DOES NOT MATTER: THE BIOPHYSICS ARGUMENT explained by circadian biology
Sachin Panda has come along 15 years after me and is telling the world what I have been saying for 15 years is TRUE and axiomatic. Food does not matter, and neither does its caloric density or quality. When you eat (TIMING) is critically important (Leptin Rx). What you eat is almost immaterial I said that in Vermont 2018 Linkedin post with Jeff Leach. linkedin.com/pulse/what-wen…
11. Sachin does not understand why EATING must be done when the sun is out......he seems to get why eating post-sunset is a bad idea but he thinks it is related solely to fasting. IT IS NOT. He does not understand melanopsin at all. Your light environment is critical, but critical in the details of how ferroptosis causes the circadian damage. This eludes Dr. Panda's understanding right now.
He also reinforces my points about drugs and supplements and why they can be TOXINS based upon light and timing mismatches. AVOID them until you know your EXACT proper circadian context in reference to your mitochondrial biology and circadian mechanism.
Those who prescribe drugs and sell you supplements HAVE ZERO clue about these aspects of human biology. Currently, most of them are selling you things that MAKE you WORSE and they get a big advantage out of this. It keeps you unwell and feeding at their trough of new ideas to sell to you. This is true in allopathic, functional medicine, and the 'bulletproof' supplement world.
I have been warning people about these aspects of our biology and people chuckled. WHO IS LAUGHING NOW? For a decade and a half, I have been training my members to understand these counterintuitive aspects of human biology in extreme detail so they avoid these pitfalls. This is why I have always said the number one cause of illness and death is always tied to the marketing of bad products to the wrong people and they are told to use them at the wrong time of their life BY DESIGN. That benefits the marketer. THAT IS THE TAKE HOME HERE.
12. The best light to use to reverse diabetes is sunlight. When will they learn the non-linear powers built into light?
Why isn't nutritional ketosis a panacea for man? Ketosis is what we do at night when we sleep. It is not designed to be a way we live chronically. WHY? Ketosis only provides us with a brisk flow of electrons from cytochrome 1 NAD+/NADH. The more electrons you have the more oxygen you need to capture them. What happens when you have more oxygen in a cell? You create more ROS. That ROS alters signaling and leads to problems. No human was built for 24/7 ketosis via food intake. This is especially true when you consider the colony of mitochondria's ability to tunnel electrons. What happens if they cannot and you keep feeding in massive amounts of electrons? The system breaks down.
When the respiratory proteins do a poor job of this, because they are separated a further atomic distance away from the neighbors, NAD+ levels drop, oxygen levels have to drop to lower ROS risk, and SIRT 1 ratio is the result in cells.
How does ketosis fit into this scenario? If you read my book, The Epi-Paleo Rx on Amazon, you will see that ketosis is a “small critical part" of reversing most diseases, and not the be all end all. Ketosis works best when you have sunlight beaming on your skin, eyes, and gut because the UV light stimulus affects the VDR receptors in the inner mitochondrial membrane to slow ECT no matter how many electrons are fed into the system.
If you don’t understand my blogs on this topic well, you will think I have just contradicted myself in my book. I have not. Ketosis can change the flow of electrons, but it has zero effect on the electron spin or state of this subatomic particle, moreover, it has no effect on the size of the ECT protein components nor the distance between them. That angstrom distance present on the inner mitochondrial membrane between cytochromes is CRITICAL in comprehending what is really going on.
Ironically where ketosis works of us, is by narrowing the distance between the respiratory proteins in the mitochondrial electron transport that ultimately determines the speed of flow of electrons. Ketosis only augments the flow of electrons. If the electrons are in the singlet state is this a good thing? Nope. It means you build a body faster than falls apart sooner. Ketosis is an accelerator pedal of electrons only. Wellness is not based solely on electrons' quantity or its speed to get to oxygen. In fact, the fraction of oxygen that never gets the electrons is what creates the free radical signal in a mitochondrion that controls the genome.care.diabetesjournals.org/content/42/4/5…
13. You cannot recapitulate the quantum coherence just by quickly TUNNELING electrons !!!!! It will sustain life until you get every detail correct. This is why you will always hear me say, you can never reverse a disease if you do not alter the environment you got ill within. The environment determines the state the electrons are in and your diet choices control the flow from cytochrome 1 to oxygen. Wellness is not linear it is non-linear and far from equilibrium. Ketosis is only a tool in reversals to buy you some time to fix your light environment your body is being forced to endure.
Fake light (unopposed blue) causes your mitochondria ECT to slow because the respiratory proteins enlarge and the distance between then GETS larger. This slows electron tunneling by a factor of ten with each Angrstrom of increased distance! It also creates new singlet state electrons which alters the free radical message. So….…..when ECT slows, you up-regulate carbohydrate metabolism by way of AMPK pathways. You need environmental UV light from the sun to offset this free radical risk. Nature built us to work this way. All this occurs just from the change in frequency of light on your surfaces. The brain can not tell sunlight from blue light, only your mitochondria can because it is what gives electrons its spin. Moreover, alternative and ancestral clinicians are unaware of this. You no longer can afford to be.
ANSWER:
You think Uncle Jack is wrong? Here ya go.....more data that you don't have it all down, food gurus.........Ketones and lactate fuel tumor growth and metastasis - in epithelial cancer cells!!!! a "reverse Warburg effect" Oops.......just when you thought the science was settled........here comes Uncle Jack with more decentralized truth bombs.tandfonline.com/doi/full/10.41…
14. There are a lot of studies on both animals and humans that suggest it’s not only about how much you eat but rather when you eat. Light trumps food. Jack 99; food gurus 0 news.vanderbilt.edu/2020/02...n-to…
15. From a therapeutic perspective, our sun's light mechanism of action on human biological functions (gastronintestinal, hormonal, emotional stability), varies on time of day (wave form frequency), latitude (light intensity or potential), volume of skin exposure, time (duration of exposure), preparation (solar callus - melanin volume). It will be vital we (science) demonstrate the mechanism of action from receptor (eyes & skin) into human biology. We have "seen" its effect on the vagus to brain nervous systems thru neuroendocrine signaling (), microbiome, etc. My hope is we will be able to predict and identify better therapeutic interventions for specific issues as our quantum treatment(s).
I aim to do this in El Salvador with the help of @NicoleShanahan and @ZorpZK My ideas on this are way ahead of what is happening in the USA centralized Ivory Tower think tanks at Stanford, Harvard, and Hopkins who all push the BigHarma version of truth. = they are killing people daily with their ideas.ncbi.nlm.nih.gov/pmc/articles/P…
16. The same key can open the doors to heaven or hell. The environment it occurs in or the redox time stamp of the gut when it occurs decides which outcome you experience is the take home. nature.com/articles/s4158…
17. When two points are destined to touch, but a direct connection is impossible, the universe will always find another way to connect. This is how Nature uses quantum entanglement of photons to create life. If two points are destined to touch on people, the universe will always find a way to make the connection. Even when all hope seems lost, certain ties cannot be broken in Nature. Consciousness and health all link to quantum mechanisms.
THE BIOPHYSICAL ORIGINS OF DIABETES AND HYPOTHYROIDISM
Almost 80% of T3 at the paraventricular nucleus originates from the peripheral conversion of T4 in cells outside the brain. Only 20% of hypothalamic T3 crosses the blood–brain barrier directly from the periphery. This makes T3 much more important in the human brain. Melanin and DOPA can be used to stimulate T3 production in the brain even when the thyroid is defective or missing.
The more one can tan the better this ability is. Most hypothyroid/diabetic patients are horrible at tanning because their skin is atrophic due to a lack of alpha, beta, and gamma MSH. Regular exposure to solar UV light via your eyes and skin stimulates your thyroid and brain to make T3, which balances your body's metabolism. Tanning increases your metabolism, which in turn helps you maintain a healthier weight. This is all done via POMC biophysics. Anything that blocks it fattens you and ruins your thyroid function.
T3 is the biophysical manna of longevity for mammals. T3 function is the best predictor of longevity for the human myocardium and CNS/PNS. These are the two tissues that kill humans the most. You won't hear that from Peter Attia in his new book on longevity. Huberman has no pod on this. This completes the lessons I gave you about thyroid function in the cold thermogenesis series of blogs. patreon.com/posts/quantum-…
18. Last point dragging the life out of the seed oil bro science folks: If you continue to be swayed by the biochemical ideas devoid of biophysical principles of the seed oil bro's know that the omega 6 story is a nothing burger when POMC in the liver is protecting the aryl hydrocarbon receptor = To understand the leptin story you need to really read EMF 2 blog post and the current QE series on Patreon to know about how leptin really works in the hypothalamus where metabolism begins for mammals.
Melanin controls fatty acid storage in mammals = What have I said about light and opsins for 5 yrs now? The weak covalent bond between mammal opsin and Vitamin A is broken and frees Vitamin A to DESTROY all photoreceptors in mammals = RUINS all NLO = non linear optics = biophoton creation in the UV range.
Let me know when your biochemistry experts get that point clear. Your beleifs on social media really bore the fuck out of me. You are SMOOTH BRAINERS who refuse to come to the level Nature operates at and you stay at the level you FEEL comfotable with. This is the woke mind virus that mimics the pronoun krewe ruining civilization now. You are making the same mistakes they do in science.
When will you learn that beta cells in the pancreas are loaded with POMC? Why do you miss all these critical connections and focus on the wrong things consistently?
The connections will be made for you without READING the damn blogs and understanding them!!!! PPARG regulates fatty acid storage and glucose metabolism but leptin is designed to interact with it when cellular signaling is working well to make fat. All mammals make sugar and fat from light = POMC story. pubmed.ncbi.nlm.nih.gov/15114521/
19. When we are energy inefficient leptin and PPAR gamma no longer work in allosteric balance to do what evolution designed them to do. The POMC gene activated by UV light in mammals stimulates PPARG and stimulates lipid uptake and adipogenesis by fat cells normally. So high leptin levels make you fatter but store excess energy for the hypothalamus to account for. The key thing is you can tap the energy when you are LR. PPAR G is all about filling the dump truck not emptying it. Naturally lean folks never really fill it because their wide-band gapped semi-conductors create a ton of VUV-IR-A light for melanin to absorb and properly activate the leptin-melanocortin pathways in the hypothalamus that control ALL THE VISCERA in the GUT to use the energy efficiently so they never activate PPAR G.
PPAR G needs Retinoic X receptors (Vit A) to heterodimerize with it to work. So this brings the Vitamin A story to evolution........those who are LR have a real problem with Vitamin A recycling that directly impacts the RXR function. Blue light and nnEMF liberate Vitamin A from ALL OPSINS and this is why LIGHT >FOOD.
GAME SET AND MATCH.
• • •
Missing some Tweet in this thread? You can try to
force a refresh
During wakefullness our colony of mitochondria are predominantly using paramagnetic gases like oxygen and nitric oxide to live. At night time we are using diamagnetic atoms to sleep. The same thing can be found in anesthetics. @LucaTurin has been working at this puzzle for sometime. Becker opened the door with his use of magnets to put salamanders asleep with his limb regeneration studies. The key mechanism in Nature that disturbs quantum entanglement in a warm wet environment is how these atoms are used. This is what has Nick Lane's attention now but he has not put it all together as yet.
Remember in the melanin series of blogs I told you how I hacked the periodic table. This was a topic I covered in my own work 15 years ago. It is nice to see some brilliant guys like Turin and Lane work on it now.
How to tell if a substance is paramagnetic or diamagnetic. The magnetic form of a substance can be determined by examining its electron configuration: if it shows unpaired electrons, then the substance is paramagnetic; if all electrons are paired, the substance is diamagnetic.
The magnetic properties of atoms depend on whether they have unpaired electrons. Sulfur is paramagnetic, it has two unpaired electrons. Xenon is diamagnetic, due to its full shell of paired valence electrons. Melanin has some of the most unusual electric and magnetic properties in mammals. It is tied to what Becker found and it is also tied to the current work of Michael Levin at Tufts now.
2. This idea has long roots all the way back to the time of Gurwitsch and Warburg. None of your food gurus go down these rabbit holes for you.
VLECK, J. The Theory of the Paramagnetism of Oxygen and Nitric Oxide. Nature119, 670 (1927). doi.org/10.1038/119670…
3. Life, when it innovated consciousness also used specific elements to do it. Remember what I said in the COld Thermogenesis series. Sleep was the default state of life and we evolved wakefulness. How did we do it? We harnessed magnetic flux from the sun to do it. The paramagnetic atoms on the periodic table that are all favored by life all contain unpaired electrons; this means the details of life will be found in the electrons life uses. Thus, the paramagnetic atoms from Z = 1 to Z = 20 are: H, Li, B, C, N, O, F, Na, Al, Si, P, S, Cl, K.
Insights from my @PalestraSociety talk: Uncle Jack said from the stage that the first human block chain was the Sumarian text built into stone.
2. This ledger contradicts centralized science beliefs around mankind. The Sumerian Text Revealed 8 Intelligent Beings That Came To Earth And Ruled For 241,200 Years before Noah's flood. I cannot verify the story but it is carved into an ancient stone ledger.
This remarkable writing was discovered on a 4,000-year-old clay tablet by German-American researcher Hermann Hilprecht around the turn of the twentieth century.
The most contentious ancient Sumerian document gives the names of eight ancient monarchs who dropped from the sky and ruled for almost two hundred thousand years. According to the narrative, a group of eight intelligent creatures controlled Mesopotamia for 241,200 years before the Great Flood.
The Sumerians were a sophisticated civilization that existed roughly 7000 years ago between the Tigris and Euphrates rivers in Mesopotamia, which eventually became Babylonia and is now in Iraq and Syria. The scroll that detailed the listing of Sumer rulers and their reign periods was the most remarkable relic unearthed from the ancient Sumerian site in Iraq. This remarkable writing was discovered on a 4,000-year-old clay tablet by German-American researcher Hermann Hilprecht around the turn of the twentieth century. At least 18 similar cuneiform tablets were discovered by Hilprecht (c. 2017-1794 BCE). They weren’t identical, but they shared that information believed to have come from a single Sumerian source. More than a dozen Sumerian King List copies have been discovered at Babylon, Susa, and Assyria, as well as the Royal Library of Nineveh from the 7th century BC.
The Sumerian list includes the names of several generations of kings who governed ancient Mesopotamia, as well as the length and location of their reigns. The document also featured the events of the Great Flood, legends, Gilgamesh tales, and stories of antediluvian monarchs, in addition to the list.
Before the flood, the Sumerian List was as follows:
"The kingdom was in Eridug after it descended from heaven.” Alulim became king of Eridug and reigned for 28,800 years. For 36,000 years, Alaljar reigned. Two monarchs ruled for 64,800 years. The kingdom was then relocated to Bad-tibia after Eridug collapsed.
En-men-Luana governed Bad-tibira for 43,200 years. For 28,800 years, En-men-gal-ana reigned. For 36,000 years, Dumuzid, the shepherd, reigned. Three kings ruled for a total of 108,000 years. The kingship was then transferred to Larag after Bad-tibira collapsed.
En-sipad-did-ana reigned Larag for 28,800 years. There was just one monarch who ruled for 28,800 years. The kingship was then transferred to Zimbir once Larag collapsed. En-men-dur-ana became king of Zimbir and reigned for 21,000 years. There was just one monarch who ruled for 21,000 years. The kingship was then transferred to Shuruppag when Zimbir collapsed. Ubara-Tutu became king of Shuruppag and reigned for 18,600 years. There was just one monarch who ruled for 18,600 years. They governed for 241,200 years, with 5 towns and 8 kings. Then the tide came rushing in.”
How did the eight kings manage to dominate the world for 241,200 years?
There was a lot of controversy about the early monarchs’ extended reigns. Etana, Lugal-banda, and Gilgamesh were among the mythological and legendary individuals featured in the list, each reigning for an improbable amount of time. Some people thought that they were gods with a greater life span than humans. A list of the regulations and their kingship after the flood is also included.
Many people thought for a long time that the history of 8 Sumerian rulers, their impossible monarchy, the Great Flood, and their restoration with another set of monarchs after the flood were simply Sumerians’ interpretations of legendary myths. Simultaneously, several experts and authors denied this notion, claiming that the list could not be a hoax. They began to recognize some of the names on the list of rulers.
Some researchers have discovered significant parallels between the Sumerian King List and the Book of Genesis. For example, the list covered the eight monarchs that ruled for generations before the deluge, as well as the eight generations that occurred between Adam and Noah before the Great Flood. Then, after the flood, the lifespan began to decline.
Historians are still baffled by the Sumerian List enigma because it contains some strange information about historical occurrences.
What if the list is true, and the celestial gods truly did live and govern for such a long time?
What if they had the technology to extend their lives and become immortal?
Light shapes our life but how does this stone shape your perception of what you've been told to believe?
3. So many ancient mysteries and no answers.......shells = someone was eating a ton of seafood.
Why do I look at peripheral blood smears in my patients with neurodegeneration, diabetes, and autoimmunity? I know all three have mtDNA hypoxia change and I want to see if the colony of mitochondria has changed the size and shape of the one human cell that has no mitochondria. How does hypoxia change the morphology of RBCs? How does the size and shape change of RBCs predict disease phenotype in your future? Do these size and shape changes tell us about your light choices?
I’m looking for succinate accumulation evidence to prove their is low endogenous melanin production to quench the ROS/RNS at cytochrome one.
The mechanism underlying RET at complex I is a topic of critical importance to all Black Swan Mitochondriacs. One suspected mechanism is that the accumulation of succinate in the matrix generates ROS by driving Reverse Electron Transport at complex I (NAD+/NADH)
Succinate is at a TIMING cross-road between several metabolic pathways in mitochondria and plays an important role in them, functioning to collect pools of catabolic molecules and initiating anabolic processes. This is key in Kreb's bicycle region of the matrix and cytosol of cells.
The fumarate-malate-oxaloacetate pathway, initiated by succinate, is potentially the most critical metabolic cycle because it is critical in water production in the mitochondria at cytochrome c oxidase levels. In this pathway, SDH (complex II) serves as a key enzyme responsible for oxidizing succinate to fumarate and maintaining ROS homeostasis in mitochondria through the production and elimination of superoxide. Diseases like diabetes, Alzheimer’s, and Parkinson’s disease are associated with low superoxide production and melanin destruction internally. RBC hypoxia is always present in these cases. This is why I wrote the Hypoxia 20 blog on Patreon for my farm members who wanted to know why I’m one of the few doctors left who still does this exam.
2. Dysregulation of succinate synthesis is linked with malignant transformation, did you know that? I know your centralized MDs who advocated for masks did not know it. That is a process by which cells acquire the metabolic properties of cancer and this creates an altered biophoton spectra to do it.
Question: Is this also a function of hypoxia within our mitochondria?
ANSWER. Yes it is. Decentralized medicine will never push masks or make you go indoors in disease states because we understand how cells operate.
3. Normally, to circumvent the citric acid cycle, succinate is catalyzed by SDH to fumarate. If succinate accumulates from fumarate with the reverse catalysis of SDH in diseases, we often see alterations in lactate and pyruvate also begin in the mitochondrion. The source(s) of fumarate must be identified to understand the defects.
There are two critical pathways as sources of fumarate: the malate/aspartate shuttle (MAS), wherein a high NADH/NAD+ ratio (low NAD+ level at complex I) drives malate formation which then gets converted to fumarate, and the purine nucleotide cycle (PNC). These pathways have been confirmed to contribute to succinate accumulation in mitochondrion under the reverse catalysis of SDH in pathological conditions. When your doc knows better their patients do better. Few centralized MDs know better.
1. Peroxynitrite (ONOO−) is an oxidant produced by the reaction between nitric oxide (NO) and superoxide radicals (O2 − ). It is known to produce oxidative stress by virtue of LPO, methionine, and sulfhydryl group oxidation in proteins, antioxidant depletion, and DNA damage. Do you know that NO and superoxide are both made directly from light frequencies (EMF) in most cells? The most damaging EMF is not the sun but the one man has forced us to live under. LIGHT > food
2. nnEMF (hyper)activates L-Type Voltage Gated Calcium Channels in the cell causing an increase in intracellular calcium.
Increased calcium activates two enzymes, nNOS and eNOS, which are nitric oxide synthases
These nitric oxide synthases are calcium dependent and can't activate unless there is increased levels of calcium in the cell and when calcium levels increase so too do levels of nitric oxide.
Nitric oxide can work along two different pathways; one pathway is normal but the other pathway is pathophysiological.
on the pathophysiological (bad) pathway the elevated levels of nitric oxide combine with superoxide to form peroxynitrite.
peroxnitrite is a potent oxidant that causes oxidative stress. This stimulus is used to change the metabolic pathways a cell can use to operate safely. Peroxnitrite is a free radical. All free radicals have unpaired electrons and this makes them magneto-chemicals. All magneto chemicals control timing switches in cells. Those switches are all photoswitches. patreon.com/posts/decentra…
3. At 4 minutes 30 seconds he gets to this point: Listen from there.
2. Sunlight releases photons. Sunlight can shine in the bottom of an ocean because the heat from the oceans vents is still behind the power source of this heat. Heat is a form of light but we really consider it like this. Photons are the force carrier for the electromagnetic force. Light controls all charged particles. This means that light in our sun is the ONLY thing that can control charged sub atomic particles found on Earth. What kind of light does our 'G class star' emit mostly again? RED LIGHT. Where does it come from? H+. When Hydrogen is ionized it loses it electron and become H+ and it glows red.
H+ = a single light hydrogen proton. It is also positively charged. This means that red light photons from the sun can control and program things with H+ in it. This is how nuclear and molecular resonance with light works. This is why mitochondria are built in all tissues to make this light useful.
Light is capable of controlling all things with charges including the larger bio-molecules found on a planet by using light frequency in the emission spectra of H+ from a near by star to energize electrons and protons in many ways. I showed you in Reality 16 all the different ways it was possible, and in the Reality 18 blog, I told you how RED light controls H+ in all things, because ionized H+ is where all the red light is emitted from in the photosphere of the sun. This is why red light helps ALL TISSUES.
What are the implications for atoms on Earth then?
3. Modern physics cannot figure out why the corona is as hot as it is, based upon Kirchoff's law. Why should you care? Anything that affects how the sun makes light, effects our understanding of how circadian mechanisms and epigenetic mechanisms works in living systems. That is why this topic is not esoteric to a mitochondriac.
Why did I say it?
If you look at the pictures in Reality 18 blog you'll notice something unusual about the atoms in the sun. When hydrogen protons in the sun fuse they make deuterium.
Deuterium is destroyed in the interiors of stars faster than it is produced!!
In our sun (G class star), on the time scales of its creation, deuterium hardly exists at all. In fact, in the corona/photoshpere of the sun, deuterium is almost non existent. This occurs because of how the atoms collide by the solar fusion mechanism. This means because deuterium is short lived in our sun, and it means it rarely gives off its light emission signature in the sun's light. This means its corresponding light would rarely reach Earth's surface. If it can't reach Earth how could it control deuterium on Earth? Remember light can control atoms or molecules it resonates with. This is a nuclear magnetic effect. Is this why mitochondria have tight controls on deuterium? YES IT IS.
We are a few hours from my talk. This new blog is a preview of the biophysics I will discuss today.
Every wave in Nature connects with every mass in nature via resonance, and so it is with life and how we create things. ----Dr. Jack Kruse
Is there something special about how the sun creates light that is critical for a mitochondriac in training to understand? Do you know what it is? If the blood plasma connected the sun with our mitochondria by way of hemoglobin, what about the sun's light, which makes it seem so cozy with our mitochondria? Could the sun be an object that uses magnetohydrodynamic equations to communicate directly with mitochondria and use our blood plasma as its conduit? It is a provocative idea for a conventional physicist and biologist. The exciting thing is it explains many of the phenomena we see in life on this planet. The liquid plasma model of the Sun is a non-equilibrium approach to the problem of understanding how life came to be as it is. This idea supports the idea that the entire sun supports nuclear reactions, which can occur throughout the solar mass. The Standard gaseous model believes the sun is a layer of gas that looks much like the layers of an onion and uses a "thermal emission mechanism" to explain how white light is created with a continual spectrum by the sun.
This standard model has never been able to explain why the sun's surface temperature is what it is and why light emission on Earth is always associated with some condensed matter lattice state. Suppose the sun's surface acts like matter on Earth and uses a lattice to emit light. In that case, we should expect that the primary means of addressing internal heat transfer is based on convection and conduction, not thermal emission. Is there evidence that contradicts the standard gaseous model of the sun? There is. How would these ideas mesh with biology? Is this new idea biologically plausible based on what we know about the mitochondrial matrix? I believe it is. I believe bio-physics on Earth may be the key for scientists to finally realize that the creation of sunlight might be the key to fully understanding the theory of the evolution of all life on this planet. It may explain why Lynn Margulis, Woese, and Bill Martin's critical questions of describing why life is the way it is.
So what about this theory is key for the mitochondriac to know? Today's blog aims to discuss how this idea explains why the solar spectrum color palate is what it is and why red light is the dominant form in solar light from sun up to sun down. Might we finally figure out why all the critical chromophores tied to energy production inside a cell are all red light chromophores?
The unusual story of all food webs on Earth is about crystals and magnetic demarcation. Food is a story about semiconductive crystals that are hydrated. Bringing the sea to our interiors made humanity possible. This is also why the Roma Empire became a great civilization, and you can see that buried at the foot of the Trevi fountain. Did you know how these ideas are linked?
A central mitochondriac credo is "everything scales back to light, water, and magnetism........"
Today, I will show @PalestraSociety how true this is.
How does magnetism put its two cents into the food story on Earth?
Did you know crystals are a special part of matter whose atomic lattice allows for it to be loaded with tons of electrons that can be excited in place or moved by light photons depending on the energy in the light they are struck by? Do you know where crystals naturally form in the universe and are linked directly to the laws of electromagnetism?
Crystals form along the lines of magnetic demarcation set forth by the magnetic field of an object. The Earth has its own magnetic field, and the Sun has massive magnetic fields. How was food formed initially? Have you ever thought about that primordial idea? No food guru can explain it. Can a decentralized MD do it?
Food is matter designed to capture light energy from a star and transfer it to another crystalline lattice.
What are the crystals in Nature that transform starlight into food structure? Chlorophyll.
The oldest food webs in our oceans were built around chloroplasts. Chloroplasts surround an Mg+2 atom with 4 Nitrogen atoms, which are then surrounded by water. This means that chloroplasts are liquid crystalline structures that operate within the visible spectrum of sunlight. This protein has unique absorption spectra that tell us how it captures and transforms sunlight.
Chloroplasts are liquid crystalline photo-stems because the presence of water (magnetic dipole) and a spinning ATPase head creates a magnetic demarcation in a cell. This magnetic demarcation links the sun's magnetic flux to the crystal's ability to absorb magnetic energy via resonance.
Few understand that every wave connects with everything in nature via molecular resonance, and so it is with food, art, & life.
These specific resonant frequencies in the crystals with these magnetic demarcations could draw light to these crystals by magnetic molecular resonance.
This resonance phenomenon results in an electromagnetic collision with matter, creating a standing wave or an electromechanical deflection in the crystal to record information about the incident light wave. Along these magnetic demarcation lines, this waveform attenuates and collects minerals of similar resonance created by the incident light EMF. Crystals can amplify those harmonics in solar light waves and tune them in their crystalline lattice to use them physiologically.
Do you know what the harmonic of sunlight is? I discuss it in my blogs in the Reality series. You'll be in for a shock when you stop being lazy and actually read my work.
In this way, you see how the Earth's magnetic field was critical in "tuning crystals" in key light harvesting bio-molecules formed in chloroplast membranes (and RBCs and mitochondria) to create the photosynthetic cores on Earth. These photosynthetic crystalline cores make the ENTIRE food web on Earth. Semiconductors take light and reflect it to create something new from the light. That reflection is seen in food and ART. patreon.com/posts/11012141…
2. The picture form that goes with the talk?
3. What happens when we forge a country or civilization? What forces are we tapping in Nature to reflect our power?