QT#24: NON LINEAR LIGHT EFFECTS IN A 5G WORLD

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Time is basically an illusion created by the mind to aid in our sense of temporal presence in the vast ocean of space. This space is filled with currents that connect things and change things in ways few of us realize. Those electrical current vary electron clouds in us to allow our cells to perceive time by creating it. Light comes to us in a timeless fashion and few of us realize it. To see the past we must slow light down by observing it in some way. Without our cells to slow light down to create a virtual perception from these waves, the past and the future based on all our experiences, there is no actual existence of the past and the future. All that there is, is the present. As crazy as this seems, the reality is, time is always standing still because light photons are timeless; we are only changing because the things in us slowly light down and then time emerges for us to perceive. It is an illusion of our mind built by nature because of quantum weirdness.

 

 

Why does time perception vary between young and old animals in a species? The ability of a hyper-sensitive atomic lattice clock filled with time crystals is used and built by nature to determine small differences in light or in altitude is based on Einstein’s predictions in General and Special relativity. Protein crystals tick every time they are hit with light. It turns out the tock varies with the type frequency in the spectrum. In this way, time varies with the power of light ticking the crystalline protein. When it is Xrays or cosmic rays time moves faster than if the light is in the infrared when the proteins are coded for by DNA.

 

 

These universal laws predict that the farther one gets from the center of an attractor (like Earth), the faster time moves. Blue light spreads the cytochrome proteins further apart because freed Vitamin A destroys them, and this results in a non-linear collateral effect that changes matter in us. This occurs by making variable ROS/RNS, and as a result, time clicks faster in the proteins of our eye clock. The faster time moves, the older a living thing becomes. The slower the click is the younger something will remain. This showed us for the first time in human history that time truly was universally relative, but, it also shows how time relies on gravity to manifest. Gravity manifests when atoms come together and condense into something with a mass. What physics does not realize yet, that electromagnetic radiation that is highly powered can generate electric charge in matter and the resultant charge can draw matter together. Gravity is a mechanism to do this, but it is a flimsy force. The electromagnetic force draws matter together this way to innovate life. This is why MORE cosmic rays penetrate Earth more when the sun’s magnetic field drops.

This allows more cosmic radiation to enter the ionosphere to make clouds and cool Earth while making more water. Gravity is not needed in this cycle at all. In a sense, time, gravity, and the weather are all emergent properties of matter as different frequencies of light hit particles of matter in our environment!  It sounds hard to believe but it is true.

 

 

The orbit of Earth around the sun and the tilt of Earth create this unique electromagnetic anomaly to your common sense. The Earth orbit around the sun is not round, it is an ellipse. This means that it will be closer and further away in its travel around the sun in a year. This is called the perihelion. Currently, the Earth is closest to the sun in January. In fact, in January the Earth gets 7% more solar radiation because of this effect, but the Earth temperatures remain colder. Why does this anomaly exist? Well, the reason for this apparent anomaly is there is a second more powerful factor at work that changes the dynamics of the system as it turns out. In January the northern hemisphere, where most of the Earth’s landmass is is point away from the sun, even thought it is closer.

This tilts reduces the amount of solar radiation to the Northern hemisphere by close to 50% of the expected irradiation caused by the perihelion.

You should know that the perihelion is not set in stone on Earth either. The month it shows up varies over time. In fact, this determines when ice ages can occur and when they cannot. Right now the location of the perihelion is perfect for an ice age, but the other two cycles are not optimized to generate this effect. The angle of the Earth today is at 23.4 degrees, but the tilt must be at it most shallow number at 22 degrees when an ice age becomes possible. The thrid cycle that controls ice ages is linked to the shape of the Earth orbit. The ellipitcal shape varies in our path around the sun. When the orbit is at it most ellipitcal shape an ice age is more likely. All three cycles must be in phase for an ice age to occur. Today we are in a mid way position of our oval shape so an ice age is unlikely. This cycle is controlled by the cycles I wrote about in my book. We are about 60,000 years away from all 3 cycles being in alignment for the next ice age to begin.

 

 

The tilt of a planet is what creates circadian time in living systems and that circadian time is what codes for hydrated protein time crystals that will be useful on a particular planet. This helps explain why there is 500 known amino acids in biology, but on Earth life only uses 20 of them. Only our DNA codes for 20 of 500. have you ever stopped to ask yourself why?

It turns out how the sun’s electromagnetic spectrum varies as the solar system travels through space around the galaxy. Not even that variable is set in stone. The amount of cosmic radiation in space that our spiral arm in the Milky way sense where our solar system exists varies its power density as we speed through space. These things all have non-linear collateral effects on the living things on Earth, and the physics possible on the planet.

Even the tilt of Earth has massive implications for circaditan timing. When you see time this way, you begin to see just how relative time is on Earth, compared to other locations in the universe. This is the pathway of the Black Swan.

 

 

EXPLAIN JACK………….

When gamma rays hit neutrons, new matter can be made.  This is how light matter interactions can create new reality.  Does this process happen in Earth?  Yes, it does…..clouds are made when cosmic rays from space hit things in our ionosphere and that collision causes electrostatic binding of particles in the ionsophere to form and they can become the initial seed needed to make a cloud.  This experiment was done and reproduced at CERN.  High energy light forms clouds that is the basis of the hydroglogy cycle on Earth.  This paper below from 1997 in Denmark is where it all began.

 

 

Svenmark noted the following when studying the sun as pictured below. When you superimposed the solar magnetic flux over ambient cosmic radiation you see almost a complete match. This means as sunspots go away, the sun’s magnetic field lowers its power, Earth gets bombarded by more cosmic radiation. It is also why the magnetic poles on Earth begin to vary. Today, this is happening in your own lifetime.

 

 

This implies as the sun’s magnetic field power drops clouds form in the ionsophere of the Earth and those clouds block terrestrial sunlight and this is what cools the planet.  It is also what condenses clouds over our oceans.  As hot water in the oceans rises the water vapor seeks to bond to the particles made by the cosmic radiation impacts on atmospheric gases.  If too many particles are created by the interaction of cosmic radiation with the gas atoms in the atmosphere clouds will be made but not enough water molecules will bind to these “water seeds” in the atmosphere and no rain will fall.  At the same time the planet will really cool tremendously.

Conversely if just the right amount of cosmic radiation makes it through to the Earth, particle amounts will be optimized and allow many evaporated water molecules to join the “water seeds” so they get heavy enough to fall to earth as rain. Rain occurs via electrostatic changes in the ionosphere.  This is why high latitude regions have more clouds but release less rain and why tropical zones have clouds that release a lot of rain.

The reason this happens shocks people.  What if I told you thunderstorm clouds are nature’s version of Chernobyl or Fukishima on Earth to make clouds?  Would you believe it?  It is true.  This radiation has benefits for living system who rely on the hydrology cycle of Earth.

Thunderclouds can unleash many types of radiation from the electromagnetic spectrum. One type of light they emit is X-rays.  Did you know that?   It’s the same type of radiation that I use as a surgeon in spine surgery to peek inside the body.  A related form of ionizing radiation, gamma radiation, can be hundreds of times or more energetic than X-rays. Most gamma rays in the universe come from solar flares, black holes or the explosive death of stars. But occasionally, “earthly thunderstorms” unleash a monster explosion of gamma rays in our atmosphere.

The discovery of these terrestrial gamma-ray flashes — or TGFs — initially caught scientists by surprise. Earth-orbiting spacecraft accidentally spotted some of these flashes in the 1990’s. At the time, those satellites had been looking for gamma rays from traditional sources outside the solar system when we found this little surprise.

TGFs flash roughly 1,100 times a day, according to recent estimates. Each lasts a mere fraction of a millisecond. But the energy released in that short flash is huge. It’s equal to the power needed to light more than 10 million 100-watt incandescent light bulbs.

 

 

Indeed, gamma-ray flashes are so big and spectacular that scientists had assumed only certain types of thunderstorms could trigger them. But at a recent 2014 meeting, researchers from the University of Alabama, in Huntsville, showed data that seem to disprove this.

They used a gamma-ray space telescope along with ground-based lightning detectors. With this duo, the researchers identified 24 coastal thunderstorms that produced TGFs. These storms had rumbled through Florida, Louisiana, Texas, Puerto Rico and Guam. With help from weather radars, the scientists studied features of each storm as it developed.  This is part of the reason I track weather radar for TGF’s and spikes in RF when 5G pulses turn on in a city.  I believe TGF’s will be more common in 5G areas based on the things I have been tracking.  The TGF’s seem to vary with solar magnetic effects tied to sunspots.  When sunspots are not present these storms in subtropics and tropical areas seem to get worse and rain increases tremendously.  We’ve seen this effect all over the Southeast this year as 5G was turned on.

Surprisingly, a thunderstorm’s intensity doesn’t seem to matter in the the generation of gamma rays.  I have a sense 5G will be capable of stimulating these non linear events too.  The researchers found all kinds of storms gave rise to TGFs.  This is why I fully expected the switch for 5G might do the same.  It appears my educated guess was correct.  Even thunderstorms so weak that a weather forecaster wouldn’t look twice at them triggered gamma rays in these weather studies.  Once I realized this in 2014 I began to really watch 5G cities and gamma ray bursts.  I saw a link with solar changes in magnetic flux.  The events over Santa Rosa California several years ago was eye opening example of this mechanism for me.  I believe, all these things were in play to start this electromagnetic chain of events.

WHY IS THIS INTERESTING, BUT CONCERNING?

The more one flies in the subtropics the more gamma rays and Xrays you are likely to experience.  This means flying in them carries larger biologic risks than most of us think.  It also means flying about 5 G cities or in between 5G cities might be one of the more risky things one can do in a 5G world.

Considering that lightning strikes Earth about four million times each day, though, even if only 1 in 100 produced gamma rays, it means a massive array of radiation is unleashed in the ionopshere as we travel in it.

WHAT IF WE TRAVELLED INTO THE EYE OF THE STORM?

Could we learn more?  It appears researchers and NASA think so because that is exactly what an research team did in 2015.

They took a commercial aircraft — a real one — equipped it with many different sensors and sent it right into a thunderstorm.  This program was sponsored by the Dutch national aerospace laboratory.  They developed a special monitoring system for the plane. They installed it on an Airbus A380. That’s the world’s largest passenger plane that was built by a consortium of EU countries. The system detected lightning strikes on the plane as it flew in the storms. It also assessed the strikes’ impacts on the aircraft as it rumbled through the skies. Other detectors and sensors aboard this plane measured X-rays and gamma rays emitted to the plane.

The plane’s crew endured more than five hours of severe turbulence on one flight as it steered the aircraft from southern France to northern Italy in 2015. In this daring flight, twenty lightning bolts struck the plane in this first-of-its-kind experiment. Another 42 bolts struck during four additional days of stormy travel.

The Airbus didn’t catch any TGF’s. However, this study was the first to measure X-rays in thunderclouds are REAL phenomena.  This has huge implications for the real causes of diseases in frequently fliers and the routes they commonly take.  I was always worried about circumpolar routes but I realized in 2015 that flights between 0-28 degree N or S latitude is now a big issue in a 5G world.

HOW DOES EXTRATERRESTRIAL RADIATION OF THIS TYPE AFFECT EARTH?

The amount of cosmic radiation that enters the polar regions and the equatorial regions is not equivalent either as the picture below shows.  It turns out the tilt of the Earth and the perihelion of the sun and Earth determine these effects.  The perihelion of the sun and Earth is also a dynamic variable on Earth.  The perihelion is how close Earth is to the sun as we revolve around the sun in our ellipitcal orbit.  Right now the Earth is closest to the sun in January and furthest from the sun in June based upon the cycles that control this process.  These process are all linked to circadian biology of our mitochondria in ways you might not realize.  The picture below shows you how heat at the poles varies as tilt varies during these cycles.  The tilt of our planet is also not fixed.  Your mitochondrial biology is built for these variations, and you do not even know it.  Tilt is the basis of how circadian biology was built on planet Earth.  I covered this topic in my book, The Epi-paleo Rx.

 

 

Could the tilt of the Earth lead to hot spots or migration of the magnetic poles on Earth?  Yes they can.  They can vary and occassional make hot spots at polar regions because of how tilt varies with heat dissipation at the poles.  HYPERLINK

Did you know that all circadian biology links back to the tilt of the Earth? Is the tilt at the poles constant? Does the tilt of the planet somehow relate to the sun in ways we fail to account for? Did you know that tilt varies in many ways that create non-linear relationships? What might the collateral effects before our species as they vary? Are the position of the sun at the tropics and the presence of the sun within the Arctic circle linked in ways that we have not yet connected to things that are alive?  Is this relationship related to other living things too in the polar regions? Is this why trees cannot exist above a certain latitude on Earth? If trees are not here what does this mean for oxygen in these areas?  Since oxygen is the terminal electron acceptor of mitochondria what does this mean for animals?   Is this why humans have trouble at these places? Is this why humans have troble living in abandoned bunkers doing biohacks?   Is this why there is a spot under Antarctica that is now real hot that science is impotent to explain? Might the evidence of this effect be found in your brain cells right now? Is this why ‘an Ancient Pathway’ in mammals exists because of varying radiation present on Earth?  Is this why Jack wrote about these anomalies years ago?

Could all this be why I wrote the Cold Thermogenesis 4 and 6 blogs?  Are those blogs like the “rings of tree”?  Are they able to tell us something about the quantum biology of the brain as the environment varies its radiation profile in mitochondria?  Radiation is not something to fear, it is something to understand when you are Black Swan.

Radiation = a form of light = and light a form of EMF right?   Well what does this picture now mean to you as a black swan in training?   

 

 

Radiation changes the matter in us……..and that matter changes reality.  That reality is called evolution in process.  This is how life really changes biology.  Darwin was really missing a lot when he made his leap of faith.

WHAT WILL MAN MADE 5G RADIATION DO TO MITOCHONDRIA IN A BLUE LIT WORLD?

How varying radiation affects the hydrated protein time crystals in our cells teaches us a deep lesson about the risks we are going to face in a 5G world.  5G will bring us a new form of radiation to deal with.  How will it change these variables mentioned above?

So I linked a post about a hot spot under Antartica above…….what do you think might be causing it?

The linear thinker would be lead to quickly respond to the answer was a geothermal volcano. But a Black Swan would never assume this because it is too linear and easy. Nature never uses Occam’s razor in her recipes. There is nothing parsimonious about the photoelectric effect or the mass equivalence equation, is there? So what would be your guess is causing this “odd phenomenon” under our Southern Continent?

Human thinking is fools gold, when it comes to light. It falls prey to linear thinking and relationships far too often. Nothing about light or nature is linear.  For example, we’ve long assumed in our solar system that planets are formed outside stars in planetary discs “for the ‘obvious’ reason linked to our observations as humans – that’s where we find them.” in our telescopes. But then we forget about the similar relationship of creation found in our own species. Namely, we humans, equally ‘obviously,’ are outside our mothers as we live our lives – yet we did not start there!

We never stop to see this blind spot of linear thinking. We have observed the beginning of human life all the time in our own life as an internal process of fertilization and development  that becomes external at birth. With the planets in our solar system, since humans did not observe their creation, why do we assume how they are today are best explained by their current position?  Might the easy guess be wrong?  Might the tilt of planets offer us a clue on what the answer might be?

I do not think there is a geothermal unit under Antartica now at all. I think it is an electromagnetic effect tied to four variable effects of the Earth’s tilt between 21.5 and 24.4-degrees.  I think the fourth variable is the addition of electromagnetic pollution man has added to the the ionosphere that we are not accounting for in our models.  I believe the radiation on Earth connects us to the sun via the solar plasma.  I think the sun is able to sense these changes and the cycles might begin to show variations we did not expect.  Might this be why we have seen an unusual sunspot season recently?  Is this why there is a weird hotspot under the magnetic south pole?  I  believe this hot pocket varies as the tilt and the electromagnetic relationship of the sun the Earth varies.  We have strong recent data of massive migration of both the magnetic North and South Pole today in the current solar cycle. We also see the sun is now no longer on its normal 11 year cycle.  It looks like it is lengthening out to 13 years since 2005.  What do you think about all these things?

How do you think? Have you ever thought of how you think and how it affects your beliefs and perceptions? Are you a convergent or divergent thinker?

What drives your perspectives and perceptions about things you observe? What data holds your thoughts and imagination captive?

Now let me go deeper down this rabitt hole of light radiation with you.

The tilt of Earth creates a latitude map.  This map is geometric.  The tilt of our planet creates our seasons.  At the equator, were we evolved, the sun varies very little.  The further we go from the equator light varies greatly.  How is this situation coded for by our mitochondria?  How do plant chloroplasts handle this?

Your latitude determines the dose of terrestrial sunlight and radiation your colony of mitochondria receives.  This location affects your colony of mitochondria and this is codified in their electromagnetic footprint to create very specific chemicals as EMF’s vary.  The incident EMF they sense leads to a specific response in your cells.

 

 

Is this electromagnetic fingerprint buried in your skin color, your haplotype and SNP patterns? It turns out it is………….Look at the haplotype map below.

 

 

Note that were humans come from is firmly in the tropical zones. This means for 4-6 million years human ancestors have become used to a tropical climate. We left Africa about 70,000 years ago and this is when haplotype variations and skin changes occured.

 

 

It looks like all these things began to matter in us as we moved away from the equator.  It appears variation in humans might have become the way of life today just because of the tilt of Earth, doesn’t it???

IS THIS WHY HIGH LATITUDES ARE LINKED TO HUMAN DISEASES?

Type one diabetes is growing by leap and bounds and it felt to be an “autoimmune” disease.  Is it really, or are all autoimmune conditions due to defects in solar radiation?

A plot of the incidence of type 1 diabetes vs. latitude demonstrated an impressive U-shaped curve. Children younger than 14 y during 1990–1994 in 51 regions worldwide demonstrated a 10–15 fold increase in risk for developing type 1 diabetes if they were born in far Northern and Southern latitudes

 

 

Although the exact mechanisms by which solar irradiation may reduce risk for autoimmune diseases are not fully understood we do know that vitamin D plays an important role in cellular immunity based on the copious papers in the literature.  Inactivated T- and B-lymphocytes are unable to respond to 1,25(OH)2D because they lack a VDR. Most physicians do not even know that our key immune cells do not have a VITAMIN D receptor.  However when they become activated BY SOLAR IRRADIATION, it is then they express a VDR and are now responsive to the immunomodulatory activity of 1,25(OH)2D.  So if you wear clothes, sunglasses and live indoors you should expect to get an autoimmune condition based on what we know………WHY ISN’T ANYONE TOLD THIS?

 

 

In B-cells 1,25(OH)2D downregulates immunoglobulin synthesis and B-cell memory. Thus by doing so, it REDUCES production of autoantibodies responsible for causing autoimmune diseases.   Anyone with pathologic antibodies needs more sun to turn off the process.  Why don’t the functional medicine guys labbing people up to the tune of thousands of dollars a month tell people this?  Planned obsolesce is my guess.

1,25(OH)2D also has a multitude of functions in activated T cells.  Did you know the skin of humans, where sunlight is supposed to hit, is where our largest colony of T-cells are located?  This means the sun has to program these cells.  If blue light does the coding guess what you get?  You get branded with an autoimmune condition.   This hormone decreases T cell proliferation as well as the number of Th1-Th17 lymphocytes while increasing T-regulatory lymphocytes by increasing the production of Th2-Th3 lymphocytes.  Isn’t it amazing how we work, and isn’t amazing how poorly clinicians know the basics?  1,25(OH)2D also directly influences the expression and synthesis of several immunomodulatory cytokines.  It activates close to 3-6% of the human genome.

Why is Sardinia an outlier here on my picture?  Might it be they are very tech addicted and have been early adopters of technology? 

^^^^This is BIG TIME warning for 5G radiation environment.  We will see 5G changing the solar redox maps for disease generation.  This is already happening in the USA with zipcodes and tech use and we are seeing it in hospital data for close to ten years now and no one seems to know why.  A Black Swan does see it. If your skin is not in nature’s game you should expect an autoimmune condition.

Its a huge deal when you consider that with any exogenous microwave use as 5G technology requires.  These waves of light will create manufactured storms in our local environments to make everything that is an insultor or a conductor far more conductive than normal.  This collateral non-linear effect makes jump conduction an even bigger problem for our skin.  5G adds microwaves to pulsed RF radiations to operate.  It turns out with pulse modulated signals will then be able to ride on all sorts of surfaces of living things like our skin and the ground itself to cause major problems. I have measured RF riding on the Mississippi River edge where the local homeless live and at the ocean shore break of all places during one of these electrical storms.   these homeless people have begun to all get autoimmune conditions, skin problems, and many allergic reactions according the local EMS and NOPD I have spoken too.  I know why it is happening now.  They don’t.  I have told the homeless to avoid this area.  I used my meters to convince them of the conduction from the local high tension electrical wires that run at the rivers edge.

Bouillon et al. summarized that 1,25(OH)2D downregulates pro-inflammatory cytokines and interleukins (IL) such as IL-2, IL-4, IL-8, IL-12, tumor necrosis factor-α, and interferon-γ and upregulates anti-inflammatory interleukins such as IL-10.

 

 

At high latitudes the shifting solar radiation is greatest and it appears our brain works poorly when the sun radiation varies most. This points out two key factors, namely, rebuilding wellness should always follow the path of solar redox as the first step. The human brain is our species energy hog. It needs the skin in the game all the time to make sure enough solar power is present to feed its addiction for sunlight. It suffers most when energy is dwindling from our surfaces. 5G will cause topologic collapse because of how this radiation affects surfaces. The effect will be great in the skin in brain in a 5G world. Our blood plasma rise toward our skin when the sun irradiates us. 40-60% of our blood volume increases with solar irradiation. The skin absorbs what the brain needs.

 

 

Our brain requires 20% of our cardiac output, yet only makes us 1% of our mass. No other intervention should ever get in the way treatment wise of solar redox when you understand these mitochondrial relationships. Anyone who puts detox of redox should be eliminated from your panel of experts in healthcare.

 

 

Is this why living things with complex brains have issues at these latitudes? Is this why trees do not grow above the 50th latitude? Is this why people at high latitudes get more mental illness than normal?

During exposure to sunlight after previtamin D3 is produced it will absorb solar UVB radiation and isomerize into two major photoproducts, lumisterol and tachysterol. Neither affect calcium metabolism, but both effect the immune system. In fact, nature built the skin so that we cannot overdose on UVB light but we can overdose on Vitamin D3 supplements.

When human skin is exposed to sunlight it can only convert approximately 15% of 7-dehydrocholesterol to previtamin D3. Any further exposure will result in a photoequilibrium whereby previtamin D3 is converted into lumisterol and tachysterol as well as revert back to 7-dehydrocholesterol. In addition when vitamin D3 is made from previtamin D3 in the skin if it is exposed to solar UVB radiation it will absorb UVB radiation and be converted into several suprasterols and 5,6-trans-vitamin D3. These chemicals all have health effects in humans they cannot get if they do not have their skin in the game. In addition previtamin D3 can also be converted to several toxisterols. Therefore no matter how much sun a human is exposed to vitamin D intoxication will not occur because any excess previtamin D3 and active vitamin D3 is photodegraded into products that have no calcemic activity!!!

These chemicals are how we control the microbiome of the skin that can lead to other diseases.

These myriad of photoproducts have other biologic effects that might interest you, such as regulating epidermal cell growth and reducing risk of skin cancer. This is how sun exposure reduces skin cancers by controling bacteria and by improving apoptosis. One product, lumisterol, if converted to 1,25-dihydroxylumisterol has anti-tumor effects in the skin microbiome. Some of the suprasterols also have antiproliferative activity in cultured human keratinocytes and immune cells. Therefore sensible sun exposure to produce previtamin D3, vitamin D3 and its photoproducts has some additional benefits above and beyond simply taking a vitamin D3 supplement or ingesting vitamin D3 from dietary sources. this is why where you live and how much skin you have in the game matters in a 5G world.

Is latitude a solar electromagnetic fingerprint of a “quantum code” created in the immune system to allow for certain bacteria in you, on you or in the soil that allows you and a tree to stand up tall in the Taiga? What happens at the top and bottom of the world in polar regions in darkness for months at a time when UV and IR light are ABSENT?

Bacteria can help or harm us. If you match your latitude and skin properly bacteria that help you prevent skin cancer manifest. See the picture below to see the relationship. Now we have documented proof of what I have taught my tribe of black swans for over a decade now. We now have proof the same thing is true on the human female breast, with respect to breast cancer flora too. This is why all of your skin must be in the game when you are out of the polar regions. These regions are the ones that have the most bizarre light effects and this is why life is sparse above the Arctic and Antarctic circles.

Naturally occurring bacteria on our skin affects by light we live under helps protect against skin cancer – This is more fuel to the fire to avoid stripping your skin of its natural bacteria with scrub brushes, soaps, oils, and beauty products. Covering your skin chronically in areas sets the tone for the cancer microbiome. It also means being indoors under fake light might be the real problem with skin cancers.

 

 

This picture below mimics one of my patient’s skin on her breast to make the point. After she had cancer on pale breast skin she got the message, she needed to have all her skin in nature’s game to control her bacterial flora.

 

 

The same effect happens to your microbiome in your gut too, with resepct to light.  If I am invited back to Vermont in 2019 I plan on blowing their mind yet again.

Our DNA genes are not as important as our daily light habits in our environment are in determining our gut microbiome. The Black Swan Mitochondriac wisdom has been gaining more proof that light environment controls our genes and those of our microbiome. This story is congruent with Jeff Leach’s work published this year on the Hazda in equatorial Africa. I wonder when researchers will gain the insight of how our ambient light environment controls most processes in us where the microbiome interacts with our surfaces?  even the Journal of Nature is waking up.   

 

 

IS IT REALLY FOOD THAT IS DRIVING DISEASE OR IS IT THE LIGHT?

Jeff Leach paper’s showed us all in 2017 that people who live in equatorial zones can eat anything and their microbiome does not change.  It appears their bacteria remain constant because the sun at the equator is constant.  So do we have any more people who criticized me flipping their story about food to light now?  Yes we do.

Why DIETS/nutrition data really stump “experts”?

Kessler states:

“The obesity problem is worse than we’ve thought. It creates a kind of metabolic chaos…And we are clueless. We have no idea what interventions work.”

https://www.youtube.com/watch?v=a-NLAQPp_3k

Could this be that is because it is the light environment that dictates what is wise to eat and not what is available by modern standards.  This is what programs the mitochondrial nanomachines called cytochromes.

One of my readers put it wisely, “Ex-commissioner Kessler was saying, in a sugar-coated way, that the public at large is fucked by bad information. Being dependent on being told what is right and what is wrong has led most into a state of disease and subserviency. Dr. Nestle is beyond clueless and has succumbed to the Koolaid she’s been drinking for years. Most don’t realize that there is a choice. You can take the blue pill (laws of man) or the red pill (laws of nature). The truth is available to anyone who chooses to look. If you choose not to look then ye shall reap what ye sow.”

 

 

Now, let us go deeper………..what happens when cells are KEPT from the “invisible part” of the visible spectrum?  You do remember that our retina is blinded to UV and IR light didn’t you? What happens when that terrestrial solar light is physically absent on Earth because of the tilt of Earth?  The tilt of the Earth varies in cycles that traverse 41,000 years.  You do know that the further you go away from the equator the shorter days are right?   Do your eyes and skin become nonoperational in these cases? Is this why living things tend not to be fond of these locations because of how light varies so much?

I just gave a talk days ago in Mexico to a large audience of eye doctors and I used this video to explain how non-linear effects of light we do not see help improve the balance of power in the ateries of the retina and RPE to make it impossible to get a cataract or acute macular degeneration.  In the video, the wolf was the predator that changed the rivers in Yellowstone in a non-linear fashion.   Ask yourself what was the predator in my example for my audience of eye docs to show how we can improve the rivers of arteries filled with blood in the retina from the ophthalmic artery of the sick patients? It turns out it is the light we are blind to that does it.  If we saw it and observed it, this effect would never happen.   UVA and IRA light from AM sunlight transition is the “light predator” that the human eye must have to maintain its optimal health matrix.  What happens if you live in a place or make choices where you never see this transition?

 

 

This juxtaposition stunned the eye doctors because all of them were taught to believe, as I was in med school, that UV light was a predator stimulus like the wolf was thought to be in Yellowstone. It turns out this linear thinking was dead wrong when it was examined closely when unleashed in nature. Moreover, when I showed them the effect of how a “hidden light predator” from AM light could ‘tame” the retinal vessels and heal them because of the non-linear effects of UV and IR light our retina does not see on the fovea…….silence filled the room. When you know better, you can do better and think about your environment is a non-linear behavior I teach my tribe of misfits. UV and IR light act using a different meatbolism to do their dirty work too.  The fovea of the retina has to use a Warburg metabolism because there is no retinal arteries there.  UVA light is critical in this area of the retina to create nitric oxide which sharpens camera vision improves the eye clock functioning and reduces the chance that cataracts form. They key is understanding where this transition occurs in your own life based on your light choices. No two eyes are the same.

What happens if the non linear part of the spectrum are absent because of the tilt of the Earth since you live above the arctic circle?  or you work indoors because you work when the UVA/IRA transition happens?

You get AMD, glaucoma, and cataracts.

Why are no trees above the 59th latitude on Earth? Might it be why the hot spot exists in Antarctica today? It appears life can transmit energy and information well………but can it originate it? The hot spot and the mystery of the 59th latitude is a big hint that light is the key to the mystery.

My speculation is simple and linked to photosynthesis.  If the invisible part of visible light is absent for too long a period of time a chloroplast cannot use water with CO2 to make sugar or the wood a tree trunk makes.  Conversely, a mitochondria cannot break food down to CO2 or water if light is absent too long either.  Therefore life is wholly dependent on the light our retina is blind too. It turns out the quirks of the tilt of the Earth lead me to this belief.  Life cannot exist without these frequencies of light.

Just as a tree cannot make wood in its trunk without light, life cannot make water in their mitochondria to sustain metabolic proteins that need a specific type of water.  Life makes water from light using the mitochondrial matrix…….and it is the UV and IR light that DOES THIS for complex life…….but plants need CO2 and light to ignite the life from abiotic atoms via its organizational power tied to energy and information. More proof/fuel for the fire that food gurus have absolutely no clue that a broken mitochondrial engine at the cytochrome level is a far bigger deal than food macronutrients are????  I think so.

When cytochrome one in the matrix is defective, diabetes is just ONE of the possible diseases that manifest in humans. Where the damage occurs determines the disease phenotype. Excessive blue light exposure and nnEMF can cause this effect MOST FREQUENTLY. Cytochrome 1 is made from the NAD+/NADH couple.
NADH:ubiquinone oxidoreductase (complex I) plays a central role in the respiratory electron transport chain by coupling the transfer of electrons stripped from carbohydrate foods. This occurs when the food electrons are passed to NADH and onto ubiquinone (CoEnQ10). This helps create the proton gradient across the mitochondrial membrane matrix necessary for ATP synthesis via the proton channel in the ATPase. Understanding the atomistic details of the electronic wiring of all Fe/S clusters in complex I have been revealed by using the tunneling current theory and computer simulations.
It turns out both density functional theory and semiempirical electronic structure methods have been used to examine antiferromagnetically coupled spin states and corresponding tunneling wave functions to understand how variations in electrons are handled by cytochrome 1.
Distinct electron tunneling pathways between neighboring Fe/S clusters have been identified; the pathways primarily consist of two cysteine ligands and one additional key residue.
Internal water between protein subunits is identified as an “essential mediator” enhancing the overall electron transfer rate by almost three orders of magnitude to achieve a physiologically significant value. That water is made by cytochrome 4 = cytochrome C oxidase and it is deuterium depleted by design to allow for these key quantum interactions.

These key cysteine residues were further characterized by sensitivity of electron transfer rates to their mutations, examined in simulations, and their conservation among complex I homologs.
The unusual “electronic structure properties” of Fe4S4 clusters in complex I EXPLAIN their remarkable efficiency of electron transfer.  Moreover, it is NOT THE FOOD that one eats that determine the atomic interaction at all. Foods are just substrates of electrons and protons in the molecular machines and not the key actors. It is about time we wake up to these realities because now researchers can examine them.

In the early days of biochemistry, science was blinded to these actions, so it was natural to “GUESS” food mattered. Today, we know better but this information has yet to have a clinical impact or made the textbooks. There is nothing special about food electrons but there is something very sensitive and specific (quantized) about how the cysteine residues act electronically in the cytochromes.  they appear to be built to work in a highly specific way to vary electric charge in the rings of carbons of cysteine.  This electronic signature is why cytochrome q  makes superoxide in ways that it does. The pulse of superoxide is quenched and controlled by another chromophore protein called melanin. Melanin is a UV absorbing protein made of the aromatic amino acid tyrosine which also has a submolecular elctronic fingerprint.

It is remarkable that the most fundamental energy-generating machinery in atomic lattice of the cytochromes in MITOCHONDRIA is based on the WAVE properties of electrons and protons.  This allows for an efficient electronic transport of energy-carrying particles along the chain of redox cofactors toward molecular oxygen via quantum tunneling. What is even more striking is that both electrons and protons also use tilt (spin) in this process as they move and that is life’s fractal nature making its appearance in this blog. Melted water at the pole is tied to tilt and light in non linear ways that most won’t even coming close to guessing. They’ll always guess the hot spot is caused by a volcano.

Without photosynthesis possible at polar regions is there any food web? Nope. Without a source of electrons can a mitochondria move protons? Nope. Is this why sun light is needed for light?  Does this mean that cells are really perpetual motion machines for electrons and protons?  Yes.   Is this why the varying light at our poles link to planetary tile to teach us something very fundamental about life that we’ve missed in biology?

I think so.

ENGINES OVER FOOD 

If you focus on the fuel, food, and neglect the fidelity of the engine you’ll never understand how biology operates electronically. Tilt of the axis of Earth is the source of all the quirkiness in circadian biology. This non-linear relationship should astound you. When you think about it…….really think about it as I have done for 15 years you begin to see how the process links the environment to cellular processes.

Circadian rhythms provide a selective advantage by anticipating organismal cyclic needs and guaranteeing optimal metabolic capacity during active hours when the sun is out. It is wholly dependent on the invisible parts of the terrestrial spectrum of the sun. If those hours are in the sun the clocks work differently if they are in the darkness and nocturnal. Impairment of circadian rhythms is associated with increased risk of type 2 diabetes and emerging evidence suggests that metabolic diseases are linked to perturbed clock machinery and not the fuel source at cytochrome 1.

It appears the certain fuels operate the matrix better when cytochrome 1 is defective. That is it should not be carte blanche to vilify foods, as most LCHF people do. It should be the reason you learn more about the cytochrome engines that are defective because of a broken circadian mechanism. When you realize this is all tied to our planet’s tilt, you just fall back into a chair. This is the Black swan perspective. The circadian clock regulates many transcriptional–translational processes influencing whole cell metabolism and particularly mitochondrial activity.  It uses light variations to get the job done.

DNA TOO?

Most people have no Earthly idea these non-linear effects of light really affected how life was built from foundation blocks of matter found on Earth too.  Consider a pyrimidine base found in DNA.  If they look at a pyrimidine base in DNA they would see the pyridine ring is made of 5 equally charged carbon atoms and a single nitrogen atom that has a relative postive charge to the neutral carbons as the picture below shows.

 

 

The varying electric charge tells us that each atom in the base ring of this molecule experiences time differently when light radiation interacts with it but few of us realize it. The positive charge of nitrogen causes the ring to develop a dynamic positive valency of all the solo atoms in the pyridine ring. It turns out this change in nitrogen is important in the formation of clouds from cosmic radiation too. Nitrogen in the atmosphere is triple bonded. Cosmic radiation is capble of breaking it up and in that collision, the electricity created in the collision creates the electrostatic binding that makes the “water seeds” needed to allow rain to be made to allow photosynthesis on Earth to occur. Remember that the ring structure of life also uses nitrogen too in its core. Might this be how sunlight is first changed into life’s first electric signal allowing atoms to become biotic?

 

 

You need to look at the whole of the ring of pyrimidine over the atoms to see what nature is really up to, as she creates the arrow of time in the living state. It is not what most people think. Photons from our star or from space come to our pyridine rings in a TIMELESS state. Why?

Photons do not experience time. They are packets of energy that have no mass and must constantly move. Photons interact with electrons in matter. All parts of the spectrum interact with matter differently. This allows for different changes in matter that a cell can use.

 

 

Once the photon interacts with the electrons ring time manifests and it manifests in a way tied to how this charge is distributed in the DNA base ring. The classic formula and 2-D drawing of the pyrimidine chemical ring above gives you an idea of shape and chemistry it never reveals why or how nature is really using it. This is why medicine is fundamentally blind to the actions of light in most things in biology.

The 2-D formula tells and predicts the dipole moment of the ring but the atomic diagram gives every chemical a personality and profile that has a high degree of specificiity and sensitivity we call its quantization. A molecule ability to be quantized and coherently controlled by our sun is what makes life possible. Atoms grouped together in this way begin to behave collectively and coherently in ways that examining the parts would never reveal……..this is why nature is a mystery to modern science. They have no idea how the changing charge of atoms alters atomic structure to make abiotic atoms behavior collectively to become biotic and assume a time stamp as the light that programs matter slows. It is only when light slows that the arrow of time appears.

 

 

It turns out how the electric charge is made and varies is the key to understanding what nature is doing inside of cells.

Thunderstorms and 5G can alter the charge in cells therefore they all have biologic effects.  One does not need ionization to change life’ trajectory.  The entire spectrum has different ways to change the gear shifts in cells.  It is time we wake up to it.

This is why the NTP study showed 2G RF radiations could cause cancer in nocturnal animals.  This is our wake up call……..will we get it?

 

CITES:

S. Ornes. “Where will lightning strike?” Science News for Students. Sept. 16, 2014.

T. Sumner. “Lightning strikes will surge with climate change.” Science News for Students.Nov. 19, 2014.

SPACE.com Staff and NASA. “NASA’s top 10 gamma-ray sources in the universe.” Dec. 6, 2011.

Original Meeting Source: T. Chronis et al. Radar and atmospheric sounding observations around 23 TGFs. American Geophysical Union annual fall meeting, San Francisco, Dec. 17, 2014.

Original Meeting Source: P. Kochkin et al. In-flight measurements of energetic radiation from lightning and thunderstorms. American Geophysical Union annual fall meeting, San Francisco, Dec. 17, 2014.

Original Meeting Source: D. Smithet al. Constraining faint terrestrial gamma-ray flashes with stacking analyses. American Geophysical Union annual fall meeting, San Francisco, Dec. 17, 2014.

Productivity measures are destroying patients and doctors

We do not produce anything worthwhile in medicine today. So it raises the interesting question, how does productivity measures relate to being a physician or a patient in 2018?? I do not think they relate to anything worthwhile in any circumstance. This meme was created by consultants from the business world that hospitals have used to usurp power from physicians. It is an apples to oranges comparison. Physicians work with individuals to diagnosis, prevent, treat, and hopefully improve both longevity and quality of life.

 

 

When doctors focus on productivity we begin to treat via our Rx pads and hospital algorithms/recipes built by the paradigm to harvest profits and not raise reversals of diseases. Moreover, in the process we’ve stopped educating our patients as we used to do. I changed that when I began blogging ten years ago. In my opinion, this is when we lose our edge our patients get more ill and their visits shorten because we have to trade time for money. Productivity of time leads to a paucity of good care.

According to Wikipedia, “Productivity describes various measures of the efficiency of production. A productivity measure is expressed as the ratio of output to inputs used in a production process, i.e., output per unit of input. Productivity is a crucial factor in production performance of firms and nations.”

Productivity is not a crucial factor to patients or doctors but it is to bean counters who are controlling hospitals and medical decisions in big government.

Hospitals build distractions in now for nurses, doctors, and patients via the electronic medical record. We now talk to screens and not to each other. This also increases the blue light hazard for all involved.

Being in a productive environment comes with its own challenges, such as the exposure of numerous distractions in the healthcare setting. Some of these include the constant influx of messages and emails from the EMR, which will then tempt you to answer them even if it isn’t necessary. Doing so can inhibit your productivity. In these cases, it’s necessary to make your environment conducive to productivity but this can’t always be the solution if your working environment is not in your own control. Today, we’ve lost control of the environment in medicine.

 

 

The players in healthcare also have lost much of their self discipline. Unfortunately, productivity doesn’t come naturally to some people because others are innately lacking in self-discipline. Without this trait, it will be challenging to create quality output in the space of time that makes it desirable. This is especially true in medicine. If a patient is not all in on their treatment plan, how good can we expect resutls to be. Conversely, if a doctor is treating people using the wrong ideas because evidence base algorithms’ are wrong how good will patients do in this paradigm? For example, a procrastinator MD may produce good results, but if the patient output can’t be produced within the required timeframe, because the patient has no skin in the game, it can seriously hamper productivity.

 

 

Physicians work with individual patients. We should strive to tailor care with our patients, and not some external stimulus. Sometimes that stimulus we bring to the table and it is completely counterproductive to the over success.

 

 

Productivity implies that we can count patient units. That idea really disrupts the essential “why” question?

If you are unfamiliar with “why,” I highly recommend Simon Sinek’s book Start With Why. Why did we become physicians? Why have people become patients? Why did they choose us? I think about all these things now that I am a month away from opening up a Center that will focus on quantum biology. I think the answer for most physicians includes helping individual patients. We strive to do our best for each patient, but we need to reassess things and ask, are we really doing it? If not, why not?

 

 

Where did productivity measures enter medicine?  It began when I was in medical school in the 1980’s.  Most experts believe that Hsaio’s NEJM article, “Estimating Physicians’ Work for a Resource-Based Relative-Value Scale,” led to RVUs (relative value units) which many practice administrators use to measure “productivity.”  Hsaio, a noted economist, wrote in the abstract of that article:

We found that physicians can rate the relative amount of work of the services within their specialty directly, taking into account all the dimensions of work. Moreover, these ratings are highly reproducible, consistent, and therefore probably valid.

This is where we really went off the rails in healthcare in my opinion.  Why?

However, this model has led to gaming the system, and equating RVUs with hard work or productivity.  But many physicians believe that the RVU system provides many wrong incentives, the most important being that shortening visit time leads to more patients per day and thus more money.  I’d never get paid if I wrote this Rx for every patient because the paradigm has no rewards for prevention as a productivity measure, yet it is what patients all want.

 

 

I wish physicians could just ignore RVUs and spend appropriate time with each patient. When physicians try to do this, practice administrators work to get physicians to see patients faster.

This leads to great stress for many physicians, and often unhappy patients. Many physicians believe that shorter visits (especially with primary care physicians) lead to more testing and consultations. Functional medicine believes they solve the dilemma by expanding the visit but ordering massive amounts of tests they do nothing for outcome or productivity. They are making the same errors allopathic medicine has made by replacing testing and supplements for the prescription pad.

 

 

Productivity implies that seeing more patients each day is a good thing. But likely most patients and physicians will agree that we need to optimize the time with each patient. How many patients can we comfortably see in one day and deliver high-quality care? High-quality care does not refer to performance measures, but rather complex multi-dimensional factors that improve the patient experience. For many patients, talking about the things that really matter is both therapeutic and diagnostic. When we shorten our conversation time, and focus on the wrong things we raise the risk of diagnostic errors, while increasing health care costs, and create dissatisfied, confused patients. That is where we are now, because we’ve subtracted nature from medicine.

 

 

So please join my personal movement to ban technology productivity from medicine. Technology is ruining medicine for both doctors and patients We are not producing anything worthwhile in medicine right now. We need to be caring for patients who need our full attention in this world set up to harm them from technology and an indoor existence.

 

CPC#36: CAN WE PREDICT 5G RISK FROM APOCRINE SECRETIONS?

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How?  It occurs via volitile compounds released from our apocrine glands.

An odor is a volatile chemical compound that humans and other animals perceive via the sense of smell or olfaction.  It turns out our ears are expert on making our noses perk up.  This is how senses work coherently.   Odors are also known as aromas or fragrances and (if they are unpleasant) as reeks, stenches, and stinks. The type of molecule that produces an odor is called an aroma compound or an odorant. These compounds are small, with molecular weights less than 300 Daltons, and are readily dispersed in air due to their high vapor pressure.

The sense of smell can detect odors are extremely low concentrations.

So what makes these volitile chemicals in our ears?  EARWAX does.

Ear wax is not what it seems from a quantum perspective.  It is similar to eyelashes and nose hair, your earwax is a protective device that is often under-appreciated.  It protects your special epithelium and hair cells in your ear that are electromagnetic antennas.  People with little ear wax tend to have more environmental exposure to nnEMF.

Ear wax is not wax.  It is exfoliated skin and it operates using the Auger effect to protect us from electromagnetic waves.  This cerumen substance is a combination of skin cells that have fallen off from inside of the ear, bits of hair and secretions from the ceruminous glands in the outer ear canal.

Did you know that earwax has a circadian basis tied to latitude and mitochondrial biology?  Most people are ignorant of these things.  At Kruse Longevity Center we make it our business to know these things because we begin where allopathic and functional medicine end in their understanding of human biology.

There are two different types of earwax: wet and dry.

A. Dry earwax is usually crumbly and lighter in color from tan to light grey. People that have North-Eastern Asian and Native American ancestry often have this type of earwax.

B. Wet earwax is sticky and yellow to brown in color and can even have an odor. This earwax is normally found in people that are more likely to have European or African ancestry.

The primary purpose of earwax is to protect your ear canal and eardrum from foreign materials and foreign electromagnetic waves.  Whales are mammals that have an exquisite hearing mechanism that uses cerumen because they use echolocation. If I told you we can use ear wax to assess patients for pregnenolone steal syndrome and their blue light hazard would you believe it?  Well, you better, because it can.  And that means there are many more aspects it can tell a Black Swan clinician.

Stress or anxiety can actually increase your earwax production. The glands in the ear that assist secreting wax are a class of glands called the apocrine glands. The human female breast is an apocrine gland.  These glands are the same glands that are responsible for your apocrine glands to create sweat.  This is why a return of sweat creation is part of the Leptin Rx.  They have a larger array of mitochondria that create water and also create your pheromones.  They can create massive odors both good and bad and these act as signals to other animals about your suitability for mating and immune function.

Stressful stimuli activate your PVN in your brainstem and they can make you sweat more (and smell worse to you and your network), stress and other emotional responses (like fear) can also increase your earwax production.  This is why the paper below is not a joke………it is another tool for the Back swan to use in the raod to optimal.

CITES:

CPC #35 : THE WOMAN CODE: FOOD/SKIN/MAKEUP

 

New podcast out for the Thanksgiving week for you to enjoy. In this podcast we go over some classic ideas about how food is an electromagnetic blueprint and we discuss the details linked to freed Vitamin A and how it destroys photoreceptors.

Why is colon cancer exploding in a blue light world?

Why does our skin bleach? Is it tied to hair bleach ladies use for their hair?

Catalase is one of the photoreceptors that Vitamin A destroys in Vitiligo. Artificial blue light and nnEMF cause this stimulus in this autoimmune diseases. We also talk about a lady who is a lawyer in Boston and how her job gives her melasma.

Blue light stimulates melanocytes in humans. Could this be why people are getting ocular melanoma now?

What are the collateral effects of these effects for women now?

In this podcast I lay it out for ladies.

Why do we get fat and depressed?

Why is make up bad?

Is clothing on the breasts a problem too?

Is the AM sun the key to mitochondrial health?

Why are women the key change agents in health?

Why did UV light get a bad reputation in medicine?

Does sunlight really cause skin cancer or protect us from it?

 

 

 

Where do humans live and work in the modern world?  Is it in the sun or not?  Do you use sunglasses?  Then you need to understand the “orange tree” analogy.

Does light dictate microbiome changes or is it food?

 

 

SUMMARY:

WHAT ARE THE UNSAID IMPLICATIONS OF THIS INTERVIEW?

People who have uncoupled haplotypes who can use both sunlight and cold to drive their mitochondrial biology will be better adapted for the 5G world that is now being unleashed on us.  This is a very counterintuitive implication of the ideas shared in this interview.  This means people with darker skin and eyes who have uniform levels of melanin, with L0,L1,L2 mitochondrial engines might need to consider inside the Tropic of Cancer and Capricorn to best protect themselves from the Internet of Things because they will be markedly affected by unusual diseases electromechanical hypersensitivity and disorders of their immune system.

Moreover, the use of sunglasses, sunscreens, clothing, and makeup will stress these individuals more leading to second generation mitochondrial diseases that right now remain uncommon.

What are some examples of this predictions?

Lyme, Chronic fatigue, EHS, autoimmunity, ALS, autism, childhood eye and skin diseases, fertility issues, cancer of the RPE in the eye, disorders of the gut will become common.  When these things become more common we should also expect to see more osteopenia and osteoporosis in these people too because as the 5G networks will lower RBC Vitamin C.

Very few see what the Black Swan sees because they do not have a proper perspective of how a quickly changing environment will radically alter how our colony of mitochondria respond.

When vitamin C is lowered by the collateral effects of 5G, bone cells that degrade bone called octeoclasts proliferate, and bone cells that lay down mineral and new bone called osteoblasts are not formed.  The two atoms that allow calcium and apatite to stay bound to bone colllagen lose their electrostatic interactions and this is the main reason why I expect decalcification of bones to be a marker for a 5G environment.  At the same time, these people will quickly calcify their arteries and their production of nitric oxide will drop dramatically cause more eye and skin diseases.

Eating more Vitamin C will not do a thing to help this problem because of the unique perspective I gave you in the November 2018 webinar in the topic.  The oral saturation effect of Vitamin C cannot overcome a bad environment.

Vitamin C does several non-linear things to improve bone physiology

A. It mineralizes the bone and stimulates bone forming cells to grow.

B. Dampens oxidative stress in the colony of mitochondria in your bone

C. Prevents too much degradation of bone by inhibiting bone absorbing cells.

D. Is vital in the unique collagen in bone that allows for bone synthesis

These things all begin with the quantum biologic effects that occur on the eye and skin.  I just came home from Mexico speaking to 250 eye doctors about the collateral effects of these things.  This podcasts deepens the thesis I am laying out here at Patreon.

GUESS THE EFFECT PRESENT ON THIS SMEAR?

 


My Black Swan mitochondriacs who see this film may see evidence of something else on this movie besides a WBC cell hunting down a bacteria.  Anyone want to venture a guess what the author of the tweet missed given my lectures on Patreon?

Post your guesses below.  Have an awesome weekend.

Movie credit: David Rogers. #CellBiology pic.twitter.com/qk75C8JFom

QT #23: WHY IS LIFE HELICAL?

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DNA only codes for proteins. When you think about this for a moment, it is quite odd. Life just does not use proteins to get the job of living done. Why don’t we code for other things? Is there a deep reason for this that we missed in basic biology?

Divergent thinking is the center of human creativity and most people believe we are born with it but I do not believe this. I believe we can teach people how to think more broadly by learning to examine things we do not believe or accept to see if they have merit or not. Divergent thinking can be acquired and developed skill when you get “skin in the game”. I now excuse people who sense life with tiny thinking. This brand of expansive thinking is a distinct form of higher-order thinking and it can be taught to all ages of autodidacts. “Divergents” always give themselves permission to see things differently than crowds. Misunderstanding vanish when you train yourself to ask, ‘What else might this imply’?

 

 

Glycine helps us break symmetry in nature by being the ONLY symmetric amino acid.  That idea sounds counterintuitive until you understand what nature is up too.  She hitches all of her chromophores that absorb some parts of the visible spectrum and connects them to proteins that act as tuning forks because the light waves the chromophore absorbs turns into an electromechanical wave of vibration in the protein portion of the photoreceptor.  All amino acid residues, other than glycine, has no symmetry elements.  So when they are strung together via the peptide bond they can never line up perfectly.  They must have some type of staggered alignment.  This topology makes them ideal to turn light waves into vibrational tuning forks using resonance.  Melanopsin is loaded with helical proteins and its chromophore appears to be the Vitamin A that is bound to it.  Vitamin A absorbs light and makes these helices vibrate in the eye so we know when night falls.

The general entanglement of one residue of a single chain into a second residue equivalent is done to satisfy a light waves requirement of a staggering molecule because light’s electric and magnetic components are orthogonal to one another.  Since amino acids are inherently asymmetric to one another, an order begins to appear from chaos.  Accordingly, this nanoscopic atomic arrangement dictates a rotational axis must exist in proteins.  This makes them obtain interesting solid state properties.  The protein axis builds a screw-like pitch angle by translation along the molecules axis.  Since light is only absorbed by the electrons in the chromophore the energy and information in light can be transmuted to other forms of energy without any loss as long as this energy is not thermalized back to the environment.  This is what makes photonic energy transfer appear to operate in the classic world like magic to us.  It is magic, but it is quantum biologic magic at work based upon the arrangement of atoms in precision with the 90-degree angle of a lightwave to make an oscillation possible.

 

 

When you realize what Mother nature is really up to with DNA, you begin to realize she codes for proteins that only operate with vibrational modes within the visible spectrum of light. She abhors things that make her proteins vibrate out of tune. Hence the only configurations for a protein chain compatible with what we call life are that the residues must form helical configurations. This is why all proteins that vibrate are helical. It also explains why DNA assumes this shape too.

It appears Mother Nature selected amino acids that can build corkscrew proteins that work with the corksrew light waves in terrestrial sunlight. This appears to be an exclusive relationship and explains why light outside or isolated from the solar spectrum cause signaling problems and interference in the system’s fidelity. Light is captured by electrons and we do a lot of things with its energy and information quanta before we let it fall back to the ground state. That is life’s major magic trick.

 

 

Watch the video now. The gap between learning and knowledge is called procrastination. Procrastination delays our success. This video shows you the way I traveled 15 years ago. the picture below shows you how light screws into the protein threads of photoreceptors. You need to get on the same page with me.

 

QT #22: LEPTIN RESISTANCE IS MELANOPSIN DYSFUNCTION

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Television and all technology screens are capable of making you hungry because they induce leptin resistance via melanopsin dysfunction —  and it’s not only all those Pizza Hut commercials!

People are unaware of how the new melanopsin data allows this process to occur.  When blue light or nnEMF disrupt the WEAK covalent bond between melanopsin and retinol, retinol because free from its normal tight circadian control.  When it is freed of these shackles it destroys ALL mammalian photoreceptors because Vitamin A is the ONLY Vitamin on Earth that emits light.  The light it emits changes the optical signaling of the local environment and this changes how chemicals in the cell at this location oscilate.  The oscillatory pattern is tightly controlled by nature to create the precise signal that is needed to make life and wellness possible.   it always creates a stimulus around photoreceptor light centers that create abnormal signaling.

The emission of light has to be tightly controlled in all biologic reactions.  It turns out freed retinal is the secret in life of how chaos is really controlled in cells.  Free retinal is the other side of the optical story of how leptin resistance gets humans ill.

BLUE LIGHT HAZARD = melanopsin dissociates from retinal and free retinal destroys photoreceptors = destroys optical signaling.   The lower your redox is the more retinal is released.  Here is the the BLH and frequencies laid out.

 

 

 

 

When you look at the table something remarkable about the sun should appear to you. As we approach the UVA and red frequencies in both directions the BLH drops quickly. We also now know that the BLH correlates with the free radicals made in mitochondria too.

Certain electromagnetic stimuli are more apt to release retinal in this way because of the weak covalent bond beside frequencies in the visible spectrum of light because of how electromagnetic waves affect bonds differently. This is why the microwave bands in 1G-5G pose a great threat to the retinal mechanism behind leptin resistance.

 

 

Blue light is the one that is now best identified in the literature.  Now that we know the human bond between melanopsin is a weak covalent bond we know that 1G-5G waveforms can also separate them even more easily via rotation.

Recent data in 2015 show that the Schiff base linking the chromophore retinal to the fractal melanopsin protein is more susceptive to spontaneous cleavage in mammalian melanopsins. In fact, the researchers went out of their way to note that this stability is highly diversified between mammalian species, being particularly unstable for human melanopsin.

This raises a big point.  If the bond is unstable in humans what might this mean for free retinal in tissues.  Is this how leptin resistance begins in tissues?

I think it is.  Why do I say it?

This pool of the retinal-free melanopsin molecules would effectively decrease the number of photoreceptive molecules in ipRGCs. If that was true wouldn’t melatonin levels also drop as a result?

What could cause the presence of the free retinal most frequently in modern life? One possibility is a shortage of retinal supply from retinal-producing enzymes or could it be stimuli from the electromagnetic spectrum that do it?  People forget that terrestrial sunlight on Earth does not equal the entire light spectrum in the universe.  Melanopsin was innovated by evolution based upon the light that fell to Earth from the sun as the picture below shows.  Not even the sunlight that astronauts face in orbit in the ISS is equivalent to the sun we get on the tectonic plates on Earth.  This is why they get diseases that were once rare on Earth.  Today, children are getting the same type of diseases as astronauts because of how man has usurped the electromagnetic spectrum for technology use.

Technology use and abuse cause the capricious cohabitation of the human’s mind. Nature’s harmony makes small things grow. Lack of it makes big things decay. Technology ruins man’s biologic coherence and induces degeneration of the mind/body in ways most do not appreciate.  This is why I created the twitter hashtag #mitochondriacwisdom.  

 

 

Does this coning feature of sunlight have implications for the melanopsin system in humans?   Alternatively, could the change in bonding be due to constant retinal release from the protein via cleavage of covalent bond (Schiff base linkage) with retinal (Vitamin A) by light? The latter possibility would be similar to what occurs in cone photoreceptor cells in the eye, where retinal is known to spontaneously dissociate from visual pigments, resulting in reduced overall cellular photosensitivity by destroying photoreceptors as the link above shows.

They found this via mutagenesis analyses, that this diversified stability is mainly due to parallel amino acid substitutions in extracellular regions. In the 2015 paper they proposed that the “differential stability” of the retinal attachment to the melanopsin fractal chromophore likely contribute to functional tuning of non-visual photoreception in mammals.  This means that rotational changes in the covalent bond alter its optical signaling ability.  This implies the fractal protein changes and this means it change how it can react.  This is precisely how the butterfly effect occurs when the chaos of changes appears to come from an order system but yield an wildly unpredictable result.  This was eloquently laid out in Jim El Khalili’s documentary   This is why all Black swans need to be really concerned with technology and artificial light use.  The 2015 paper is warning us that topologic effects in retinal is enough to cause optical damage to photoreceptors it is bound too.   This fully explains why blue light has been causing humans problems since we invented the light bulb in 1874.

 

 

Carbon atoms in single bonds rotate freely in organic chemistry. Rotation can occur because the heaviest electron density in the σ bond exists along an imaginary line between two carbon nuclei. Rotation does not change this electron distribution; the bond strength remains constant throughout rotation. Because rotation is possible, the molecule can have an infinite number of conformations. Conformations = size and shapes = changes the way matter operates thermodynamically. All of our proteins were designed by nature to work only in terrestrial sunlight.

With manmade light the bonds react differently and they change the conditions of existence of the molecules in us. It turns out blue light and nnEMF release Vitamin A from from the carbons in melanopsin and that freed Vitamin destroys all the chromophores that our proteins contain. the picture below shows many pictures of those varied chromophores in us. When they are damaged, they cannot absorb light to make the protein they are connected to vibrate properly in cell water. This ruins the resultant vibration and coherence. This is leads to disease. Leptin is one such chromophore found in your subcutaneous fat. Once it becomes defective it cannot send its optical information to the hypothalamus and you get ill as a result.

 

 

We’ve believed that melanopsin was only present in the eye since its discovery in humans since 1998. We then discovered it in human blood vessels in 2014.

 

 

Then, in December 2017 we got the shock data it was also in our skin and subcutaneous fat helping explain why nature put leptin, another photoreceptor molecule, in our subcutaneous fat.

 

 

Leptin is designed to take optical data from the skin and skin arteriole surface about day and night and couple that with energy balance information and deliver it to the hypothalamus under the cover of darkness. Free retinol from surface light at the wrong time of the day is what ruins this hormones behavior optically. Once leptin signaling is disrupted by circadian mechanisms, the hypothalamus loses control of all growth and metabolism inputs. This leads to many chronic human maladies such as obesity, diabetes, and metabolic syndrome.

This is how I solved my obesity issue 15 years ago when I was 360 pounds. I realized that when leptin was altered by alien light in my environment it changed the the atomic structure of leptin. This small change lead to massive changes in my body mass. The reason made sense. Mitochondria create heat, which is infrared light. We need this light to activate the DDW our mitochondria make. What happens if the mitochondria in me were being destroyed by light in my operating room? What do the laws of physics tell us about heat and size? small objects in nature have a different surface area compared to their volume inside. This means that smaller people lost heat quicker. This is true in planets as it is in people. This is why Mars magnetic field from its interior dynamo died out sooner than Earth. It is smaller, so it loses heat faster. Humans who have mitochondrial damage because of the damage in their heme proteins in their cytochromes would lose a ton of heat if this would be allowed to continue. What does the body do to offset the loss? It makes you fatter. Why? This changes the relationship of the surface area to your interiot volume and improves your thermodynamics while the engines inside of you get worse by the retinal damage of leptin and your cytochrome proteins. This is also why mammals fatten in winter when the sun power varies and you lose more heat to the environment as the temperature around begins to fall. Eating carbohydrates in a falling solar environment fatten you. The cold causes you to use that fat to warm yoruself until the sun comes back in spring. That is how the forces of nature work inside of you when you are leptin resistant. When I realized this for the first time my life changed forever. This was the answer to my obesity crisis.

 

 

Mitochondrial photoreceptor damage are all defects in optical signaling caused by Vitamin A’s ability to destroy photoreceptors.   This is why the the authors in the article make this statement, about blue light, ”It’s toxic. If you shine blue light on retina, the retinal kills photoreceptor cells as the signaling molecule on the membrane dissolves.”    

That is a definitive unequivocal statement made in this paper.

 

What aggravates this effect in modern humans? The human choice to live indoors with blue light and nnEMF.

Your TV is likely the greatest blue light emitter in your house after Obama changed TV signals from analog to digital in 2009.  But every tech device was digital the day it was created.  The sheer number of both devices is what is accelerating modern humans diseases now.  Nobody sees where the pieces fit until they do.

Blue light, via the photoreceptor melanopsin, disrupts autophagy and mitophagy, as I laid out in my Vermont 2018 video.  This, in turn down-regulate apoptosis (programmed cell death) in cells. Thereby, defective cells, running at a net energy loss, send out a call for more food via the defective leptin photoreceptor.  That defect is cause by free retinol in the tissue and in the blood stream that is not circadian controlled by retinol binding protein — Leptin is loaded with these aromatic rings and the light emitted by the Vitamin A alters the quantum HUMO-LUMO rings and this is what blocks leptin from going from your subcutaneous fat around midnight when it is supposed to be dark to enter the hypothalamus to deliver this photonic and electronic data to this part of the brain.  Without the proper message energy balance and metabolism is lost.  That is what leptin resistance is at the quantum level.  Because of the melanopsin dysfunction, the information and energy transfer the hypothalamus requires can never be satisfied in the mitochondrial matrix of the cells affected by this optical deficits due to their defects having escaped the recycling autophagy program built into cells.  That cycle is controlled by the circadian mechanism which Vitamin A has hijacked.  The antidote to blue light in nature,  is 42% of the red light in sun.  It is augmented by UVA and UVB light.  These parts of the solar spectrum strengthen mitophagy and apoptosis to return physiologic law and order back the the defective tissues.   We would be much better off watching the sunrise and the sunset than watching TV, using a computer, or talking/texting constantly on a cell phone,  especially at night. We’d be more wise to use a geothermal pool, or build a green house, or stare at the flames of a campfire…to stimulate the healing powers inside your colony of mitochondria.  This is the credo of the black swan.  This explains fully how I see Leptin resistance develops in humans.

SUMMARY

Leptin resistance is a photonic process in human biology. So what does blue light and nnEMF lead to give what we’ve learned about melanopsin/retinal links? It ruins the Bazan effect to ruin the long loop to cause liver level leptin resistance. This blocks DHA to be replaced in cell membranes in the liver and CNS/PNS. This causes many communication and memory issues via a broken circadian mechanism via the eye and skin. The pic is about the eye but it was created before you knew melanopsin/retinal was in the subcutaneous fat and skin arterioles. See the pic below = Leptin resistance at liver level = lowered global DHA in liver cell membranes that induce PPARγ-target catalase expression and reduce ROS levels, leading to the inhibition of JAK2/STAT3 = what leptin resistance is inside a cell below the pathway level of Ph.D. or MD understanding.

NOW YOU HAVE THE ENTIRE THESIS.

 

NOVEMBER 2018 WEBINAR: 5G HIT; WHAT TO DO?

The predictions I made 5 years ago about blue light and nnEMF will now be tested on humans. If you live in California pay attention to the news now in your local area. Why? I think the first people who will know something is amiss in our environments are ER physicians and ICU nurses and hospitalist doctors who begin to see infections that devolve into sepsis rather quickly without much warning. 
Sepsis mortality is remarkably high and likely will skyrocket in a blue lit 5G world because of how the immune system is controlled by Vitamin A.  This disease process will be very pronounced complication in American cities with 5G.  The onset will be acute and it maybe teethered to other normally inconsequential diseases.  The situation in these cases will turn dire quickly. The latest surviving sepsis campaign guidelines in 2018 has told clinicians that sepsis related mortality is around 15% while septic shock is associated with 40% in-hospital mortality and in poor countries, the mortality goes even higher up to 60%.  I expect that number to flip in a 5G city.  Why?  Hospitals are loaded with light and technology that increase the liberation of Vitamin A from melanopsin.  In those hospitals more technology is used in ICU’s and operating rooms so length of stay and length of surgery will be key indicators of who is at risk.  When you layer this with redox status of the patient pre-sepsis it will become obvious who that at risk people will be to clinicians eventually when they begin to understand the links to why this is happening.
Thousands of interventions have been tried over decades failed to improve sepsis survival in healthcare. Even drugs that were able to reduce mortality in one study, failed to do so in another study.
Moreover, my expectation is that in these patients, clinicians will find that most antibiotics, antivirals, and antifungal medications will be impotent for the patients situation.
For the observant family member or healthcare professional this should be a sign to you that the underlying cause  of the infective process might not be what the blood cultures reveal, it maybe the action of free retinal in the tissues causing destruction of optical signaling in the immune systems cells.
It will appear to the nurses who are taking care of your family that the drugs normally used are having no effect.  At the same time there will be tell tale signs that melanopsin dysfunction is the real cause of the septic state. 
SIGNS:
1.  Quick onset of decline
2. Extremely low Vitamin D level
3. Very abnormal BUN/CREATINE ratios
4. Very abnormal hormone panels.  These will never be drawn in a hospital setting until physicians learn why it is happening.  Vitamin A and T3 are cofactors that convert cholesterol to most of the hormones under the pwer of the visible spectrum of TERRESTRIAL sunlight.  If Vitamin A running wild no sex steroid hormones can be made.  DHEA-S will usually be low.
5. Procalcitonin will skyrocket in these cases.  This protein is a biomarker that exhibits greater specificity than other proinflammatory markers (eg, cytokines from melanopsin dysfunction).  It will be one of the best tests in identifying this acute destructive Vitamin A pathology in patients with sepsis that seem to confound the physicians at the bedside.  I believe it can and will be used in the diagnosis of these technology induced infections.
6. B12, thiamine, Vitamin C and folate levels will be extremely low because glucose metabolism is all that the matrix has left in acute mitochondrial poisoning.  That effectively is what melanopsin dysfunction is. 
7. Anemia onset will be rapid and the RBC count will have changes in the RDW and MCV/MCHC.  Hemolytic anemia will be more common than we see in more chronic Warburg shifted diseases. 
8. Rapid onset of capillary and vascular damage will occur seemingly out of no where because Vitamin C formation from glucose goes to zero because Kreb’s bicycle cannot operate any longer in these states.  The timescale of the decline helps explain the effects.
TREATMENT:
The 5G cocktail that will show remarkable benefit within 24-48 hours will be an intravenous mixture of vitamin C, thiamine and stress dose hydrocortisone.
Rivers of ink have been spillied in the critical care literature on sepsis.  the same is true about oxygen delivery and fluid responsiveness as key therapies in these cases.  5G sepsis will require even faster metabolic resusitation because of how Vitamin A destroys photoreceptors so rapidly that decipher optical comminications in metabolic pathways.  Heme is the key chromophore to understand.  Heme proteins are one of the oldest photoreceptors in all living things.
Restoring oxygneation and intravascular volumes are clearly important in all cases of sepsis but the rapidity of mitochondrial destruction and redox power is the key to understanding why the treatment of 5G sepsis HAS to be thought of differently.  Acute critical care teaching has cause physicians and nurses to focus on easily observable phenomena at the bedside in these cases, but that focus has led healthcare professional to ignore something of greater importance: metabolic resuscitation of acutely dying colonies of mitochondria in a patient with nnEMF toxicity.  Effectively, that is what 5G sepsis looks like and is.  It presents as acute rapid mitochondrial failure in organs.  The critical care team has to learn the hard lesson that their treatments can deliver all the oxygen we want to the hypoxic tissues, but if the colonies of mitochondria are failing in the tissues, it just won’t work.
The early use of Vitamin C will protect blood vessels and RBCs from melanopsin damage and acute proton dislocation in the mitochondrial matrix by UCP2 dysfunction and to improve their ability of RBC’s which will acutely lose their Vitamin C levels in melanopsin dysfunction due to their photoreceptor (heme and aromatic amino acids) damage which alters the ability of RBC’s to deform their size and shape to allow them to navigate damaged vascular beds to improve oxygenation.
Sepsis from electromagnetic pollution is a state of acute mitochondrial failure on a large scale in many organs and it will be linked to many stressors of the PVN.
Sepsis in one of the clinical situation we see in humans where glucose based metabolism exists exclusively.  This is not a common situation.  Beta-oxidation and the urea cycle are damage severely in this case.  The damage is greater than we see in cancer.
In humans, Vitamin C is created from glucose shunting.  When glucose is the only fuel you can use to remain alive, it is not too difficult to see why Vitmain C drops like a lead baloon.   In animals that synthesize vitamin C natural (not humans), synthesis is normally downregulated exactly in fasting or low-carbohydrate conditions, or when glycogen is otherwise low.  Notably, this is not the case in hibernation, where the reverse is true.
Sepsis is a unique clinical situation in humans.  Humans do not need exogenous Vitamin C much at all because they are omnivores and can live off of fat and proteins without any carbohydrates at all.  This is what separates them on the primate tree, but this has massive implications for a 5G world.  Why?
Blue light and nnEMF environments increase glucose in the blood by increasing the AMPk pathways (Volkow and Frey).  This means under nnEMF humans have to use glucose and cannot burn fat or protein well.  
What are the implications of this?  
Since the literature clearly shows that vitamin C synthesis is downregulated when food or carbohydrates are low suggests the following possibilities for humans in an altered EMF environment. First, it suggests that vitamin C might be more necessary in a glucose based metabolism than in a ketotic one.Sepsis is one of those situations.
Second, it suggests that there are compensatory mechanisms that come into play when vitamin C is low that are also triggered by low-carbohydrate conditions, and therefore, vitamin C requirements are lower in low-carbohydrate conditions.  People who crave carbohydrates at home are sure to have melanopsin damage somewhere in their system when you understand the clinicial implications of this blog.   This means that people who are 100% carnivorous may never need vitamin C because their matrix has very little chance of being destroyed by the deuterium in carbohydrates.  UCP-2  is another chromophore that can be destroyed by free Vitamin A to let deuterium into Kreb’s bicycle.
Third, it suggests that high levels of vitamin C, when a 100% carnivore,  might be quite detrimental under low-carbohydrate conditions.  I can tell you I have seen this effect in functional medicine patients who were given Meyer’s cocktails and got violently ill when the prescriber did not understand that the person was very ketogenic to begin with on a nutritional basis.
What is the point of this dance, Jack?
When your mitochondria is running on solely on glucose, Vitamin C become critically important in the kinetic flux of protons in the matrix.  This is the context non-Black Swan clinicians RARELY comprehend.  The more blue light and 5G tech you use, the more Vitamin C your system needs to remain well.  This is why sepsis is important to understand.  In a septic state, from melanopsin dysfunction, you will be OBLIGATE user of vitamin C.
In 1975, this was shown in a paper by Newton and Mann.  They showed that diabetics appeared to mimic a localize chronic form of scurvy.
Why is this data important especially because it was in diabetics?  Diabetes is destruction of heme in the cytochrome proteins of the matrix?  Is shows you biochemistry is completely light dependent.
What happens on the surface determines how it can operate in cells below.  It appears our essential micronutrients are very dynamic in different light environments in reference to nnEMF and retinal. Your skin’s intereaction with incident light is involved in the biochemical reactions happening inside of your matrix all the time.  You have no ability to control this process.  It seems Mother Nature set the system up like this for a reason (Quantum Zeno effect).
How much of ANY micronutrient is linked to the incident EMF your skin and subcutaneous fat senses from your environment.  Since your skin is the largest organ in your body, and melanopsin/retinal are in your skin coupled to leptin, this begin to shows us how metabolism is controlled by the light we live under.  We have the ability to alter our needs significantly depending on the light your surfaces sense.  This is why this slide showed up in the Vermont 2018 talk.  
Vitamin C can be spared by something that takes over one of its functions, or by something that increases its effectiveness.  Iodine is one such substance for humans via the Grotthuss mechanism, for example.
Human cells are expert in creating glutathione from cysteine if redox power is decent.  In sepsis it is not.  Therefore, in this situation,  glutathione offers no Vitamin C buffering because sepsis is a situation when your entire colony is failing.  Mitochondrial functioning has to be half way decent to get this effect.
Ketosis helps create glutathione in humans but it requires an intact redox state.
Sepsis is a condition where humans face the worse state of insulin resistance one could fathom.  In this state, Vitamin C can save their life when it is threatened.  It turns out, Linus Pauling might have been correct about Vitamin C in a blue-lit nnEMF world we’ve created.  He was clearly wrong in the world he lived in…….dominated by the sun.  Why?  because sunlight allows the matrix to make water and CO2 easily because it restores redox power.  Today that is no longer true.  Blue light and nnEMF do the opposite.  It looks like his hypothesis is now the way of all Black Swan’s in training.
I have a sense when 5G hits big time we might have to add uric acid and glutathione and iodine to the sepsis cocktail for survival.  Why uric acid?
Humans and other  primates share is a loss of function of the uricase enzyme. Uricase breaks down uric acid, and the result of this mutation is higher uric acid levels in primates. There is some decent data this helped the apes live longer.  It seems evolution used this mutation like she used the loss of vitamin C synthesis in primates, for a selective advantage.  I think that advantage was tied to the loss of hair on man compared to apes.  This allowed their skin to sense more incoming UV light. Hair is an light antenna but too much of it would have limited the UV input at the surface of the skin.
I think apes lost Vitamin C first, then uricase, before humans replaced both with iodine from the marine chain and made the point moot.  In sepsis, this evolutionary dance might be the difference between life and death in a 5G city in a hospital ICU.    
Many people do not know that Vitamin C is a co-factor in the formation of catecholamines and CORTISOL and those chemical all have aromatic amino acids with photon traps inside them.  This makes them targets for retinal knockout.   If you have a low dopamine state……….pay attention right now.  
Intestinal absorption of vitamin C is saturable.  This means taking it orally won’t work!!!  Given the increased metabolic consumption of Vitamin C in critical illness like a 5G sepsis, the only way to replete Vitamin C in this context is intravenously.  The effect of Vitamin C on mitochondrial damage is also born out in what Tanaka found out in 2000 in patients with sepsis.  When IV Vitamin C is used patients needs less IVF’s.  The reason is simple but Tanaka and critical care professionals still do not understand the reason.  Mitochondria end product is water at cytochrome 4.   Redox power at NADH needs to be around -400mV.  Glutathione helps keep this there.  DDW is what can help this situation in 5G blue light toxic states. 
This restores metabolic balance of Kreb’s bicycle.  When this happens the voltage drop in mitochondria from NADH to oxygen is off a cliff and it happens fast.  This is how 5G will discharge our batteries.
Tanaka found patients in the vitamin C group required less fluid resuscitation, had higher urine output, and developed less wound edema.  That is what I call evidence of matrix salvage by improving the proton problem in the matrix by nnEMF.
Thiamine will be found to be very helpful in those with severe lactic acidosis from the mitochondrial damage of free running Vitamin A.  Vitamin A will attack and destroy the heme proteins in the cytochromes just as it did in the circulatory system.
Acute thiamine deficiency decreases the pyruvate flux to the Krebs bicycle so it increases the production of lactate by altering the aerobic metabolism as the pic above shows.  This is the key sign of the fastest Warburg shift a clinician will ever see in their career.  Cells with acute lactic acidosis become unable to use the TCA or urea cycle for any metabolic functions and this is why; Krebs bicycle is demoloshed by all the heme damage in the cytochromes.
The stress dose of hydrocortisone will be important in preventing severe acute adrenal insufficiency because of the acute onset of the pregnenolone steal syndrome and to support rapidly dropping coritsol levels to maintain life.  Cortisol in this case, is the critical hormone that 5G will zap quickly.  Vitamin C also reverses the oxidation of the glucocorticoid receptors so the steroids work.  This is why Vitamin C has to be given with the correct meds in sequence.
The effectiveness of this therapy will be measured best by the PCT clearance.  PCT clearance is measured by the initial PCT drawn in the ER and then we subtract the PCT values at 72 hours divided by the initial PCT value and then we multiply this by 100 to give us a percentage.  
SUMMARY
Infections caused by Vitamin A dysfunction from melanopsin dysfunction will be called drug-resistant cases by hospital personal.  Pay attention to these catch phrases.
In these cases, it won’t be that the drug does not work……it will because the mechanism of action is light-based from the liberation of Vitamin A on all photoreceptors and the antibiotic cannot stop the release of retinol from melanopsin fast enough in the skin due to how 5G interacts with the skin’s topology. Just watch and see if I am correct now.
 
CITES:
1. Michael DH, Andrew M D. Management of Sepsis and Septic Shock.JAMA. 2017;317(8):847‒848.
2. Ranieri VM, Thompson BT, Barie PS, et al. Drotrecogin Alfa (Activated) in Adults with Septic Shock. N Engl J Med. 2012; 366(22):2055‒2064.
3. Bernard GR, Vincent J-L, Laterre P-F, et al. Efficacy and safety of recombinant human activated protein C for severe sepsis. N Engl J Med. 2001;344(10):699‒709.
4. Annane D, Sébille V, Charpentier C, et al. Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock. JAMA. 2002;288(7):862‒71.
5. Annane D. Hydrocortisone plus Fludrocortison for Adults with Septic Shock. N Engl J Med. 2018;378:809‒818.
6. Sprung CL, Annane D, Keh D, et al. Hydrocortisone therapy for patients with septic shock. N Engl J Med. 10;358(2):111‒24.
7. Venkatesh B, Finfer S, Cohen J, et al. Adjunctive Glucocorticoid Therapy in Patients with Septic Shock. N Engl J Med. 2018; 378(9):797‒808.
8. Marik PE, Khangoora V, Rivera R, et al. Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Severe Sepsis and Septic Shock: A Retrospective Before-After Study. Chest. 2017;151(6):1229‒1238.
9. Wu F, Wilson JX, Tyml K. Ascorbate protects against impaired arteriolar constriction in sepsis by inhibiting inducible nitric oxide synthase expression. Free Radic Biol Med. 2004;37(8):1282–1289.
10. Cruickshank AM, Telfer AB, Shenkin A. Thiamine deficiency in the critically ill. Intensive Care Med. 1988;14(4):384‒7.
11. Costa NA, Gut AL, de Souza Dorna M, et al. Serum thiamine concentration and oxidative stress as predictors of mortality in patients with septic shock. J Crit Care. 2014;29(2):249‒52.
12. Donnino MW, Carney E, Cocchi MN, et al. Thiamine deficiency in critically ill patients with sepsis. J Crit Care. 2010;25(4):576‒81.
13. Donnino MW, Andersen LW, Chase M, et al. Randomized, Double-Blind, Placebo-Controlled Trial of Thiamine as a Metabolic Resuscitator in Septic Shock: A Pilot Study. Crit Care Med. 2016;44(2):360‒7.
14. Jihad Mallat, Lemyze M, Thevenin D. Do not forget to give thiamine to your septic shock patients. J Thorac Dis. 2016;8(6): 1062–1066.
15. VICTASTrial.org
18.  https://www.ncbi.nlm.nih.gov/pubmed/11500168  (repeat of Mann and Newton)

QT#21: DOES MITOCHONDRIAL WATER HAVE A MEMORY?

video
play-sharp-fill

 

 

Can water have a ‘memory’ of its previous solutes, environment or processing?

On the surface, this question sounds like quackery and pseudoscience.  But the Black swan will go deeper than most to examine the evidence for themselves as the video above shows.

Montagnier experiments showed the effect.  But he still has no idea how it happens.  Today I am going to share with you how I think it does happen in your cells.

Water forms crystals that varied depending on the environment they sense.  The electromagnetic radiations in that environment can change the crystalline structure of water at the atomic level.  We know crystals are capable of creating memory.   So, is the question as crazy as it first appears?  What does the DATA say?  All systems may retain a memory of their previous treatment, whether this is due to the formation of stable contamination, or to the production of energetic heterogeneities. It has been shown that the physical properties not only depends on the initial temperature but also on kurtosis; the distribution of the particles’ kinetic energies from the mean value, a property that may depend on its past history. It should not be surprising that water also may retain a memory of its past history.

 

 

Are evolutionary changes stored magnetically in water around DNA?

In the literature it is well known that microwave irradiation gives rise to a memory effect on the surface tension of water that lasts for minutes after the effect of temperature rise alone has ended. Most scientists and the public have no idea these papers exist but Black Swans do. The first LINK below shows this effect in cite one.

This is why 5G concerns Black Swans. Microwaves induces topologic effects on water. This means it can affect its electric abilities in any aqueous system. CELLS are such a system.

 

 

More data to worry about: An extraordinary paper authored by Nobel prize-winning Luc Montagnier has described memory effects in aqueous DNA solutions that the authors propose to depend on interactions with the background electromagnetic field. These effects, if real, require the prior processing and dilution of the solutions and are explained by Montagnier as molecular resonance phenomena with nanostructures derived from the DNA and water.

So how could this happen in reality?  Is there an explanation?   What is the biophysics below the cell level a Black Swan can study?

Might the crystals in water vary in their electric abilities based upon the light around the water?  Yep.  Is water ferroelectric?  Yep.

Ferroelectric materials are characterized by the spontaneous electric polarization that can be reversed by inverting an external electric field. Water molecules are dipolar and thus ferroelectric alignment of water molecules is conceivable when water freezes into special forms of ice.  Spin ice experiments were discussed on my blog years ago.  But now the new data published in early 2018 have raised the bar for the evidence.

Did you know that EZ water (exclusion zone) and ice share a lot of physical similarities?

Generally, ferroelectric materials have high dielectric constant.  The EZ has a dielectric constant of 160 whereas regular tap water dielectric constant is only 78.

So it appears the water made in a mitochondrial matrix creates is a thin ferroelectric crystal.   Ferroelectric materials have a spontaneous dipole moment which can point up or down.  But does this unique ability explain WHY water MIGHT store memory?

Yes it does.

Being a ferroelectric crystal means that they can ALSO be used to store information, just like magnetic bits on a hard disk. The advantage of ferroelectric bits is that they can be written at a low voltage and power.  The brain works at 20 volts.   Magnetic bits in your tech gear require much larger currents to create a magnetic field for switching, and thus more power. The disadvantage of most ferroelectrics is that the aligned dipoles are only stable in fairly large groups, so if you make the crystals smaller, the dipole moment eventually disappears.  When light hits the water, it builds a large EZ ferroelectric crystal that is uniform.

 

 

The common denominator in ferroelectric studies has been size and scale.  This is no surprise to anyone who listened to my April 2016 webinar on what constitutes life.  Water is a huge part of how life happens. In physics research, we know initially small crystals become ferroelectric, whereas larger crystals lose this property.  This is exactly how ice and EZ water are initially built.  So it does appear water made in the mitochondrial matrix is quite special because it can create a memory of things found in it.  This might explain why the Kreb and urea cycle are designed by nature to be in this water.  It appears the memory of the seasons on Earth can be magnetically stored in matrix water by its deuterium content.  Might this be how metabolic rate of dofferent tissues is programmed in morphogenesis?  I think so.

Is our circulatory system important in delivering memory to our cells by using water as its currency?

 

 

So to answer to the initial question this blog posed is: Can water have a memory? The answer appears to be yes. Why? Because water is ferroelectric at the nanoscale. When water is below 1.4 nm inside of a cell some rather bizarre things begin to occur at the quantum scale.

 

 

This means that very ‘small bits’ can be constructed from the crystals in EZ water. Furthermore, when a particular substrate is added to water that is magnetic, and this combination of magnetic and ferroelectric bits brings an extra degree of freedom, allowing each bit to store double the information. Could this be why the mouths of all the cytochrome proteins have iron-sulfur cores? Are they key to how life stores energy at low voltages and creates memory?

Does this imply that memory and consciousness might be a function of how good the water our mitochondria matrix creates is?

Yep.

 

 

CITES:

1. H. Parmar, M. Asada, Y. Kanazaw, Y. Asakuma, C.M. Phan, V. Pareek and G. M. Evans, Influence of microwaves on the water surface tension, Langmuir, 30 (2014) 9875-9879;M. T. Amiri and M. C. Amiri, Comment on “Influence of microwaves on the water surface tension”, Langmuir, 31 (2015) 10931-10932; H. Parmar, M. Asada, Y. Kanazaw, Y. Asakuma, C.M. Phan, V. Pareek and G. M. Evans, Reply to comment on “Influence of microwaves on the water surface tension”, Langmuir, 31 (2015) 10933-10934.

2. Yingfen Wei et al, A rhombohedral ferroelectric phase in epitaxially strained Hf0.5Zr0.5O2 thin films, Nature Materials (2018).

3. https://phys.org/news/2018-08-barrier-material-quirk-telecommunications.html

QT#20: UV light and salt improve sleep and health.

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Salt levels control the exclusion zone of CSF. Iodine helps augment this affect via the Grotthuss mechanism. It is the single most key mechanism in the brain. Time for our group to bone up on Dr. Gerald Pollack’s work and how it links to proton spin and information transfer to augment autophagy during sleep. Blue screens and RF/microwaves pulse decrease salt in the CSF.

 

 

Salinity and water have a deep link for energy and information generation and plasma in our cells. Most food gurus have no idea why this is the case.

Artists use lies, to tell the truth about life. Because of belief, you usually find something true about yourself in their work. That small parable of truth creates a human unwillingness to delete that belief. Wisdom is not expecting people to understand what the artist intent was; it was the anticipation of how the ideas are perceived that matters.

 

 

When dealing with living things, one can best feel how primitive today’s bio-physics truly is. Mother nature was undaunted by the huge amount of work she needed to employ by designing cells. Such a task, on the surface, might be indistinguishable from a miracle until you realize she had all the time in the world, all materials one could need, and quantum mechanics. The environment is designed to create a “decoherence stimulus” in the mitochondrial situated in the sea buried within your cell to slightly alter the complex quantum situations built into living cells by Mother Nature. Those slight changes in the exclusion zone of the water plasma surrounding a mitochondrion alter the % heteroplasmy to drive evolutionary trajectory towards the environment. Night and day are different environments. One promotes wakefulness and the other promotes sleep. The EZ is the key change to that environmental change.

 

 

Seawater is the ultimate plasma of life. It is also why every cell has salty water inside of a cell. If the sun shines down on the water and some of it evaporates, the salt is left behind and the water will become saltier. Similarly, if some fresh water is added, such as from rain or melting ice, the salt will be diluted and the water will be less salty.

Salinity does change with depth, but the way it changes depends very much on where one happens to be. That’s because of another property of water, its density. In our cells density can also be augmented or subtracted from because of deuterium.  In the brain and CSF deuterium has to be tightly controlled because of the fast metabolic rates of the TCA and urea cycle in the brain.  If too much deuterium enters the cytosol of neurons cognitive haze and poor sleep result.  Deuterium changes the density of metobolic water.

Density is how “heavy” a parcel of water is. And “heavier” water tends to sink and stay below “lighter” water (have a look at this answer from our archives for a little more on how that works).  In the CSF space this is not good because the lowest level of CSF rests on the pia mater and the surface of the necortex which is the most metabolic active tissues in our body.

The density of seawater depends mostly on how much salt is dissolved in it (more dissolved salt = “heavier” seawater), but temperature also has an another effect on hydrogen isotopes in water. In all cases, raising the temperature, invokes thermal vibrational and entropic effects. This tends to preferentially stabilize H+ over D bonds in aqueous solutions.

 

 

Pressure builds heat (IR) and heat moves things with mass. Deuterium has more mass than H+. We also know heat favors H+ bonding over D bonding in an aqueous heat bath like a cell. Heat flows from hot to cold and comes when electric and magnetic forces are confined to a tight space. This is the advantage that mitochondrion seeks to gain for cells. Heat expands most things in nature, but not all things.  Water happens to be one of those things because of its massive heat capacity.   Life uses water for this key reason, and mitochondria have chosen to release heat to water a mitochondria makes for one specific reason:  because heat shrinks water that is confined in small spaces and breaks nature symmetry by shortening the distance of the respiratory proteins on ECT.  This increases energy efficiency and proton flows in cells favoring H+.  This helps keep deuterium in the blood plasma where it belongs and not in the matrix where heat is liberated and metabolic water is made.

How does nature use this in sea water?

The abrupt change in temperature at a thermocline occurs because of the density of water changes as a function of temperature. The density of water links to proton spin in seawater. Pure water, sans salt, has a maximum density at around 4 degrees C (3.98 if you want to be fussy). Of course, in a lake, the densest water will be found at the bottom, with less dense water overlying it; this point was expanded in Ubiquitination 5 blog to a great degree as it relates to Rayleigh Benard convection. This type of convection needs a small amount of gravity to flow.  This is present on Earth but absent in space.  This is why astronauts are at risk for deuterium damage of their Kreb’s bicycle and sleep impairment with long flights.  These convections in heated water represents the lowest energy state on Earth, which is the way the physical world generally likes to be. This is why energy in water always flows or cycles naturally without any physiologic work needed to be added by a cell. A cell takes advantage of this physical property of water to innovate life.

Now then, if you imagine the sun shining down on a lake, the water at the surface will, of course, begin to warm and change the surface temperature in relation to the deeper cooler water.  Now think about what happens on your skin in UV light.  This heats up the surface quick and it also affects the blood plasma below because UVA light increase NO to make vessels come closer to the surface to be irradiated by sunlight.

This sets up the convection cell naturally I mentioned above. That will make that water less dense in certain places in the arterioles to give us laminar flow in the center of the artery (thus more buoyant), and it will be more turbulent on the surface.  That turbulence help libertate NO in vessels.  When these things occur the less dense water in blood will, therefore, float over the cooler water below it. The cooler water below has more electron density because it is denser and the surface water has less electron density in it.

The hydrogen bonding networks in both densities of water are also different and so is how they work with the photoelectric effect. This tells you their charge and size of their EZ will differ too. This is the critical physical part a mitochondrion is built to sense inside of our cells. In the ocean or lake, it is important to the ecosystem and all things that live in it. Why? Because the warmer the temperature of the water,  the more it EXPANDS to build pressure up in the skin and it loses density and gains buoyancy.  This has a big effect on the deuterium in our blood.  This thermal and hydraulic pressure make deuterium emit a full spectrum of ELF-UV.  This light can change the density of the water content of blood because the EZ has an increased viscosity and an optical window at 270 nm.

This is why water everywhere on Earth will float on the deeper cooler water below.  This happens in the sea and in your blood.   Energy in water columns flows from cool to hot because of convection. It turns out, it is not easy to move heat downward in the water column (pelagic water), and that is what causes a very sharp thermocline we see in oceans especially in the poles and Gulf.  In practice, be sure there is a small amount of heat conduction by the water, as well as mixing by the surface winds, and that will cause some LOCAL “thickening” of the thermoclines when we measure them in lakes. Remember lakes and oceans are the different. The Gulf is different from the ocean too because of salinity and its deuterium content.  This varies with latitude.  Temperature also varies with latitude.

Essentially the same thing happens in the open oceans, but there is the added complication of salt in the water (which also has an effect on the density of seawater), and very substantial wind mixing that tends to make oceanic thermoclines a little less distinct than we see in lakes, rivers, and reservoirs. So, if water has more salt in it, it will tend to be “heavy” and will tend to sink. And often there is an increase in salinity with an increase in depth in polar waters. Life there takes full advantage of this.

Life at the surface of the sea takes advantage of its local environment and your mitochondria take advantage of this version of plasma in your cells in a similar fashion because salinity relates to charge and to energy flows. All these little details your food gurus are clueless about. All that links to time. Why? charge and time are fundamentally linked by our surface topology. ‘Now’ is a local theory of what’s happening presently, cobbled together using bits of news from the sensory receptors all bathed in saline water.

Jack is there any new data to support this position?

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More proof that studying nocturnal mammals has no place in the study of human neurologic disease based on new data. Why? How much do you know about information quanta and how it operates the universe and in cells via light waves? If you do not know a think about it you might want to read my Quantum Thermodynamic series on Patreon. Information quanta is a key feature of this blog series. These neurons, unique to humans, deal exclusively in the distribution information quanta over the surface of the human brain called the neocortex.

In the end, science is just a progress report of where we are now in our understanding. It is not our final destination, but it is a data point on the road to understanding. That has been and will continue to be the message of my work.
Where we are today in science, in understanding how the brain really works, is close to where a man was 2,000 years ago in trying to understand how the planets moved in relation to the sun. We are nowhere close to where we should be.
So if we are that far away in our understanding of the brain, how can we begin to make sense of it all? We can learn a lot from the macrocosm of space if we scale it to biology on this planet. Today ’s post does that for you, the black swan, who have never heard of this information before. This post is why you need to be part of the tribe who digs deeper than your current health EXPERTS.
The human brain is surrounded by water called CSF that is generally deuterium depleted. Deuterium has a much higher density than water made of regular protons called protium.
I showed you earlier in my many free blog series on my website how molecular oxygen is delivered from the phytoplankton in the photic zone (surface) of the ocean to the ocean depths using the density of cold water to deliver it there. The denser the water, the more oxygen is dissolved in it. The power of the sun’s photoelectric effect splits electrons from water in phytoplankton, which liberates oxygen and electrons. The same thing happens in melanin in humans. Humans have melanin in their brains and more of it than any other mammal on this planet. Ask yourself why evolution would do this?
The liberated O2, in the ocean, becomes more dissolved in colder water by the laws of nature and chemistry, and then it is distributed all over the oceans by the thermohaline currents.

I have been showing you FOR YEARS how the exact same process that happens on the surface of the earth is fractally designed on your own neocortex of your brain.

 

 

HOW TOPOLOGY OF EARTH SCALES TO YOUR BRAIN

The very same process that works in the thermohaline current works in CSF that surrounds your brain to bring higher oxygen levels to the surface of your brain using QED principles linked to LIGHT, WATER, and MAGNETISM.

 

 

It uses the photoelectric effect for animal photosynthesis using many proteins. Melanin is just one protein. The unusual thing is melanin is present in the human brain in many places when we know the UV of the sun does not and cannot get to the surface of the brain. Why would nature do this?

I believe the answer is because neuromelanin is a key to information quanta transfer. It is critical in all neurologic diseases in humans.

Recall inflammation is a measure of pH in water. pH is a log scale of hydrogen protons and includes deuterium and protium fractions. Moreover, when inflammation is present and is rising for ANY REASON at all in the brain, the result in this surface of the brain’s CSF is to alter the density of water that sits above this cortex. This is what these neurons are doing. No one else will tell you this or be able to explain in detail how the process works by my members and Patrons will.

Did you know that UV light exposure of water increase the charge in water? Did you know CSF is a ultrafiltrate of blood plasma that does get irradiated by sunlight. Might this mechanism be the reason why melanin was put in the brain by Mother Nature? Melanin is a fluorophore protein that absorbs UV light. This paper below published in March of 2018 was a game changer for Black Swans.

 

 

Inflammation makes CSF less dense, and when CSF is less dense, the laws of physics control the action of biochemistry that is possible on our surfaces or deep in our tissues. Deuterium and protium have markedly DIFFERENT density measures. When you know better you do better. Time to join my tribe folks. This helps explain why UV light exposure of the eyes and skin helps improve sleep. It changes how much energy and information can be stored in the water in blood plasma that eventually becomes CSF that surrounds our brain. Salt increases the electric potential of the water in our blood plasma. It really helps if salt is used liberally by the black swan.

 

 

SUMMARY

These sensory receptors only absorb the energy and data of just a part of the environmental story going on around your 5 senses; What you are is what the brain perceives is a partial version of true reality. This is akin to biochemical data that is irreproducible that so many “closet scientist/clinicians” like to spew.  From those senses, our brain fills in the missing parts to create a story we call reality and life…….as we lose cellular charge time speeds up, we lose health, and we age faster and our sleep declines.  The fastest ways to cause this is chronic technology use.  We all need a technology diet more than we need a food diet.

This points out why some people cannot decipher data in biochemical journals well. Their sensory receptors are attuned to the wrong things because their environments are pulling charge from their senses and their brains. This lowers their information assimilation abilities in their neocortex.  Deep truth bombs here in the cite below.

 

 

Here is my key point to you: any set of labs are not good enough tools for the science we need to study to get people well. What we observe is not nature in itself but nature exposed to our method of questioning. Cells seem to use light to know about nature in ways our mind or senses cannot observe. The answers never manifest on labs either.  Labs contain clues for the quantum biologists.  This means you really need to understand light to every understand how we work.

CITE:

http://sciencenewsjournal.com/amount-salt-brain-determines-sleep-cycles/