Month: January 2023

The incidence of diabetes will rise as people block the sun and introduce alien light to their lives. And this information will be transferred to their offspring via trans-generational epigenetics and we will continue to see the incidence rise of juvenile diabetics.

Many have asked me how I believe this process occurs.
Here is my answer.

The Nobel Prize for physics in 2016 was given for the discovery of topologic insulators (TI’s).

Topological insulators conduct electricity on their surfaces but do not conduct the current deep inside their cores. This limitation allows the cell to control Brownian motion in the cell to maintain the low entropy state.  A low entropy state is critical for wellness.

This helps explain why DNA’s surface is highly coiled and coated with histones, chromatin, and methyl groups when it is kept in its “quiet state” (non-dividing)

It also explains how it can receive photo-electric instructions on its surface and transfer that information through the hydrogen bonding network (proton tunneling causing flickering) that surrounds nucleic acids to run the epigenetic programming it contains deep within. What happens on its surface can awaken the code of life buried deep below its double helix that is filled with fermions = electrons, protons, and maybe neutrinos!

This process is all possible because DNA AMO structure is capable of inducing a change in base pairs by altering the hydrogen bonds on its surface because of how Dirac fermions operate.  What is a Dirac fermion?

In physics, a Dirac fermion is a spin-½ particle. Take a look here to see a video on how I think this happens.  Electrons, neutrinos, and protons have that spin quantity.

https://www.instagram.com/p/CnPiUugho2Z/

Spin is a quantum-mechanical property, akin to the angular momentum of a classical sphere rotating on its axis, except it comes in discrete units of integer or half-integer multiples of ħ. The proton, like the electron and neutron, has a spin of ħ/2, or “spin-1/2”. So do each of its three quarks that make up a proton. With the proton, there is a catch. And that catch is one of the keys to how evolution code is altered.

Summing the spins of the quarks that make up a proton to get the total spin of the proton seems, in principle, straightforward: if two of the quark spins point up, while the other points down, the down spin will cancel one of the ups, and both sides of the equation should be left with an angular momentum of ħ/2.

Except it isn’t that simple. In 1988 the European Muon Collaboration (EMC) at CERN shocked the physics community by announcing that the sum of the spins of the three quarks that make up the proton is much less than the spin of the proton itself. This was unexpected because the summing-up approach had worked for several of the proton’s other properties. For example, the proton’s electric charge of +1 can be accounted for by adding the charge of its two “up” flavored quarks (+2/3) to that of its one “down” quark (–1/3).  (Note that here, “up” and “down” are names of quarks and have nothing to do with spin.)

However, the EMC researchers discovered that the net spin of the three quarks actually accounted for no more than 24% of the proton’s spin, and might even contribute as little as 4% – practically none of it, in other words.

It was an observation that shocked the world.  To me, it meant Nature was using spin as some coding mechanism in cells.  This unique feature would make it ideal to create a code.  Today I think The proton spin problem is evolution’s cosmic wand……

HOW DOES LIFE COMMUNICATE WITH THE COSMOS?  “THE FERMIONIC CODE”

In condensed matter physics, low-energy excitations in graphene and topological insulators, among others, are fermionic quasiparticles described by a pseudo-relativistic Dirac equation. I think DNA acts like a fermionic quasiparticle. Fermions include all quarks and leptons and all composite particles made of an odd number of these.

Some fermions are elementary particles (such as electrons), and some are composite particles(such as protons). I think this is why mitochondria only deal with electrons and protons inside of them. I also believe this is why neutrinos might be a player in biology on Earth.  Neutrinos are part of the fermion family of Nature. I think fermions and light interactions are how starlight is transmitted to living cells. This science is based on AMO physics as a discipline.

The Standard Model recognizes two types of elementary fermions: quarks and leptons. In all, the model distinguishes 24 different fermions.

There are six quarks (up, down, strange, charm, bottom, and top), and six leptons (electron, electron neutrino, muon, muon neutrino, tauon, and tauon neutrino), along with the corresponding antiparticle of each of these.  Protons are made from quarks.

HOW DID I DECODE THE FERMION MESSAGE?

Claude Shannon taught the world that information flows via entropy. All clocks should be thought of as flowmeters for entry. This includes the biological circadian clocks in cells. Wheeler taught physics that information and energy are one and the same thing. Shannon’s mathematics from his 1948 paper advanced the linkage of entropy and information. Shannon’s paper also told us anything can be a message.

I believe sunlight messages for mitochondrial DNA and nuclear are controlled by “fermion messaging”. DNA is informed about what to do with optical information from the sun via mtDNA signaling (optical and free radical) and this message is transmitted over water’s hydrogen bonds adjacent to proteins in a cell. DNA is a very complex topologic insulator that is an antenna for our star’s information.

Unlike its much larger counterparts, which we’re all familiar with in modern devices, this minuscule genetic molecule (DNA) isn’t made to transmit radio waves, but to glean the secrets of ever-changing proteins.  DNA is around 20,000 times smaller than human hair. It also emits all frequencies of light in the visible spectrum of terrestrial sunlight, which means it uses light signals to record and reports back information.

And those light signals can be used to study the movement and change of proteins in real-time.

Part of the innovation with this particular antenna is the way in which the receiver part of it is also used to sense the molecular surface of the protein it’s studying. That results in a distinct signal when the protein is fulfilling its biological function.  It also means the signal is low fidelity when the protein is not functioning well.  When this happens the cell emits another optical signal and marks the defective protein for removal with ubiquitin.

This system operates just like a two-way radio that can both receive and transmit radio waves, the DNA nanoantenna receives light in one color (frequency), or wavelength, and depending on the protein movement it senses, then transmits light back in another color, which the cell can detect and perform a physiologic function.  (Cite 2 below)

DNA chemistry is relatively simple to program and easy to use once programmed.  DNA is surrounded by water.

Water makes up 99% of molecules in every cell. Water is a very small molecule that has more hydrogen bonds in it than any other compound. Liquid water contains the densest hydrogen bonding of any solvent, with almost as many hydrogen bonds as there are covalent bonds and hydrogen bonds in its structure found anywhere on Earth. These two bonding networks are the binary code in water. Just as a computer can use a 1 and 0 to create digital information on the internet, hydrogen bonds create the internet in your cells. Shannon taught us the information content of any kind of message could be measured in binary digits or just bits.

Water’s hydrogen bond network changes at a pico and femtosecond level in any environment. Inside a cell, its atomic arrangement is controlled by electrostatic forces in a cell created by the redox power of the mitochondria in that cell. These hydrogen bonds can rapidly rearrange in response to, light frequencies, charge density, and changing conditions and environments (for example, solutes like K+ in a cell).

Shannon demonstrated, contrary to what was commonly believed in the 1940s, that engineers could beat their worst enemy ever: transmission errors-or in their technical jargon, “noise.” Noise is anything that disturbs communication. It can be an electric signal in a telephone wire that causes crosstalk in an adjacent wire, a thunderstorm static that perturbs TV signals distorting the image on the screen, or a failure in network noise to increase the energy of the transmission signals or send the same message repeatedly-much as when, in a crowded pub, you have to shout for a beer several times. Shannon showed a better way to avoid errors without wasting so much energy and time: coding. Nature does the same thing.

She takes the message in the hydrogen bonding network of water that surrounds every protein and encodes that information in “a fermionic code” in mRNA, mtDNA, RNA, tRNA, and DNA.

Coding is at the heart of information theory. All communication processes need some sort of coding to limit the noise and create a high-fidelity signal that doesn’t degrade. Water preserves the information and transfers it to nucleic acids via hydrogen bonds. Just as the telephone system transforms the spoken voice into electrical signals. In Morse code, letters are transmitted with combinations of dots and dashes. The DNA molecule specifies a protein’s structure with four types of genetic bases. Digital communication systems use bits to represent or encoded information. Each letter of the alphabet, for example, can be represented with a group of bits, a sequence of zeroes, and ones. You can assign any number of bits to each letter and arrange the bits in any way you want. In other words, you can create as many codes as desired. Cells have done this to run life’s program.

The interactions of electrons in a solid or liquid crystal change space in abstract ways. If you look at the picture below you can see odd shape and size changes and this leads to the different thermodynamics of what is possible on the surface. Many TI’s developed “holes” where electrons are absent and this allows them to act as P-type semiconductors then there are adjacent regions that are extremely electron rich that can act as an N-type semiconductor.

Those positive and negative regions can act like “charges” and can lead to striking effects. For example, an insulating material (phosphorus) can become conductive at its surface when light hits it.  All semiconductors become conductive when light hits their surface.

Phosphorus has ten atoms that stick directly out from the surface of DNA when you look at it from an axial view. See figure C below. Those ten atoms are surrounded by 447 water molecules to form part of the TI in DNA. The addition of phosphorus and iodine in the liquid crystalline water networks creates a “playground of charges and spins” in fermions to control how DNA should react to the electromagnetic signal from our star on its surface.

Note the ten phosphate groups sticking out of the surface of DNA to bind with coherent domains in water as DNA unwinds above.

Within the heavily condensed and coiled state DNA structure tightly holds atoms (lowering entropy), electrons, and photons in one “spin state”. When DNA is uncoiled by electromagnetic signals from our mitochondria hit on DNA’s surface.  This surface change can alter protons deep inside of DNA to change how it functions.  Hydrogen bonds occur between the two strands and involve a base from one strand with a base from the second in complementary pairing.

Once this change occurs light is/can be liberated from the double helix and the surface template of hydrogen bonds in water surrounding DNA radically changes the “topologic signals” by the altered spin states of fermions (protons) in the DNA crystal. This can turn on and off DNA replications. It can also cause DNA base changes.

In their seminal paper from 1953, Watson and Crick proposed that the tautomerization of DNA base pairs could produce stable errors in the genetic code. The proposed mechanism for such tautomerization was the double proton transfer along the hydrogen bonds within base pairs, Guanine–Cytosine (G–C) or Adenine–Thymine (A–T).

The tautomerization process involves the relocation of protons, which are subatomic particles and obey the laws of quantum mechanics.

Tautomers are structural isomers (constitutional isomers) of chemical compounds that readily interconvert. The chemical reaction interconverting the two is called tautomerization. This conversion commonly results from the relocation of a hydrogen atom (proton) within the compound.

The spins of electrons/protons (H+) can not only be manipulated by magnetic fields (mitochondria) but also by electrical fields (proteins side chains) and can be used to collect and store information from electrons or the photons they carry. All magnetic drives use spintronics today to magnetically store data on hard drives. It appears DNA uses many of the same ideas but it does it on hydrated carbon-based semiconductors in cells.

SUMMARY

We already know a leaf can do it via photosynthesis and so can a European Robin using a light inclination magnetic compass in its eye. In my humble opinion, this process works in all animal tissues to create the many species of animals we all observe in the classical world we inhabit.

Why don’t we have more data on this mode of information transfer in cells?

Specifically, the job of the antenna is to measure the structural changes in proteins over time. Proteins are large, complex molecules that carry out all kinds of essential tasks in the body, from supporting the immune system to regulating the function of organs.

However, as proteins rush about doing their jobs in cells, they undergo constant changes in their structure (protein bending), transitioning from state to state in a highly complex process scientists call protein dynamics. And we don’t really have good tools to track these protein dynamics in action today.

Experimental study of protein transient states remains a major challenge because high-structural-resolution techniques, including nuclear magnetic resonance and X-ray crystallography, often cannot be directly applied to study short-lived protein states.  I expect this to change as centralized healthcare realizes these tools will make Big Pharma superfluous to the public.

Topology is a branch of mathematics focused on the fundamental shapes of things as they change. In cells, proteins can vary their size and shape based on the light energy that is added or subtracted from their bonds.

In this way, life can be considered a quantum computer that is working in parallel with a quantum universe that also runs on light. The fermionic messages are information buried in terrestrial solar light wave frequencies in the sun that can be magnetically stored in a thin film of water surrounding nucleic acids, using non-linear aspects of light. DNA is the ultimate topologic insulator or superconductor suspended in a superfluid of coherent and noncoherent water that imprints information and conducts electrons, protons, and photons in different ways.

This Nobel Prize may soon get biology away from its “solution-based ideas” in biochemistry books and push them toward quantum biology which uses a solid-state foundation. That is what the Nobel Prize meant to me in 2016. The state of fluctuation of the hydrogen bonding network that light brings creates probabilities in a cell. Light adds charge density to the AMO structures in a cell.

PHYSICS IS THE SCIENCE OF PROBABILITIES. BIOLOGY IS THE STORY OF THE IMPROBABLE AND BIOLOGY CAN ONLY MAKE SENSE FROM THE PERSPECTIVE THAT THE LIVING STATE IS ONLY PROBABLE ON EARTH USING REACTIONS UNDER SUNLIGHT WHICH ARE STATISTICALLY IMPROBABLE anywhere but on Earth.

Knowing is just not enough. Understanding the connections is critical in understanding what life is doing below the cell level. Stop being your own worse enemy. Stop looking outside for solutions when the wisdom you seek is buried within you in how you organize matter in your cells with sunlight.

This is why diabetes is exploding globally in the modern world in my opinion.

CITES

1.  https://pubmed.ncbi.nlm.nih.gov/33949935/

2. https://www.nature.com/articles/s41592-021-01355-5

3. https://pubmed.ncbi.nlm.nih.gov/21457072/

4. https://pubmed.ncbi.nlm.nih.gov/35949615/

5. Watson, J. D. & Crick, F. H. C. The structure of DNA. Cold Spring Harbor Symp. Quant. Biol.18, 123–131 (1953).

6. https://www.nature.com/articles/s42005-022-00881-8

7. Löwdin, P.-O. Proton tunneling in DNA and its biological implications. Rev. Mod. Phys. 35, 724–732 (1963).

8. Löwdin, P.-O. Quantum genetics and the aperiodic solid. In Advances in Quantum Chemistry(ed. Löwdin, P.-O.) Vol. 2 (Academic Press, 1966).

9. Slocombe, L., Al-Khalili, J. & Sacchi, M. Quantum and classical effects in DNA point mutations: Watson–Crick tautomerism in at and GC base pairs. Phys. Chem. Chem. Phys. 23, 4141–4150 (2021).

10. https://www.mdpi.com/2624-960X/3/1/6

How many doctors and nurses feel like the dog in the video above???

How can a video of a caged animal help a human healthcare worker?

How will they learn to extricate themselves from their cage……how do they deal with the learned helplessness from their education?  What do I mean?

I realized 20 years ago, like a 40-year-old centralized neurosurgeon I was back in the same predicament as this dog below was.  My brain and mind were no longer my own.  They were tethered to a centralized medical mindset given to me by my education.

This educational paradigm was my cage.

The dog below fought like hell to get out.  I had to fight like hell to become decentralized.  Have you tried to unlearn to relearn?

Back then I was intellectually impoverished, unable to cure myself, so how I could really help anyone else if I kept doing the same things over and over?  I knew I had to think differently.

The dog was wiser than I was.

This is when I first began to think about building a virtual private practice and hospital.  It has now morphed into what I hope the Kruse Longevity Center to be in El Salvador.

Medicine has kept me tethered to a life that was harming me and my family.  I did not see it.  I never realized how being up all night on call every third night for 25 years was harming me.

Like the caged dog, when the tether was bent and opened initially, we often don’t realize that we have the opportunity to roam free from our self-created prison.  The dog seemed to know it right away.  Why don’t we?

Was this learned helplessness built into me by design in how I was taught to think by my education?  Medicine allowed me to escape being a poor kid in NYC, but it allowed me to build a new prison with more money, but less time and time had to be spent awake at night under fake light 24/7.  I realized slowly 15 years ago I had traded one prison for another.  It turned out the second prison was far more dangerous than the one I escaped as a kid when I thought about it.

Medicine was tethering my reality because my ability to think was usurped by an Oath I took.   My oath and education were tethering me to ideas that were no longer useful to me or my patients.  I began to feel what I believe the dog in the video is feeling.  This was learned helplessness now becoming angry and determined.  Initially, it was depressing,  and it lead me to become angry.  I became so pissed off I planned my escape.  The dog did the same thing.

Like the dog who trusts his master, a master who locked him up, he did nothing but accept his fate initially.  Initially, I did nothing to try to break free on my own either.  I hate the idea that, as an educated medicine man, felt I had to blame somebody for this educational disadvantage.  It never occurred to me I was my own worse enemy until much later in my professional life.

I hated the notion that I, a modern doctor, lacked the ability or means to take control of my own destiny.  This is why when I see a caged animal video, I remember this lesson.  When I woke, I ripped the tether from my life as the dog did below.  I realized quickly I was fully able to step outside the downward spiral I was in. I realized I could fly again if I took control and became the CEO of my career.  Even today I often think of those many animals who are caged and how their perspective shaped their future life as slaves to a paradigm.

I wonder if centralized doctors and nurses realize how their job traps them.

I wonder if their patients understand how it affects their care.

I wonder if centralized healthcare workers understand why so much junk science is published these days.

The answer is simple:  There is no cost to being wrong in modern centralized science, but there is a huge cost to not publishing if you are part of the centralized paradigm.

What lesson have I learned about my profession in 2020-2022?  The COVID experience has taught me that there is an inverse relationship between education and common sense. The higher you go in academia the less common sense can be found.  This is why the PEER-reviewed literature is littered with junk science.  

The American dream is alive and well in centralized healthcare. The hustle is sold separately to patients individually in a package called “evidence-based medicine”. Corporations force mandates down our throats that the government cannot do due to illegality. And it’s funded by the guys making money on both sides of the equation.

Science must always be “pressure tested” to distill the truth. That’s the only way forward.  Science isn’t ‘what experts think.’ It’s a method that corrects what experts think.  In 2021, Fauci claimed he was science.  In 2022, the scientific method has removed him from power.

I believe you will learn why alternative therapies and natural immunity were removed from the lexicon of medical science by bureaucrats in 2021-22.  The jabs cost them a lot of money to develop and they needed to protect themselves from legal challenges to the EUAs if any alternative therapy worked because this would have made their EUAs ILLEGAL.

A curious principle of epidemiology, which only the public seems to get and the elites act like it is a conspiracy theory is what happens if you give drugs that work too late in the course of a disease?

What we found out in 2022 is that ‘scientific authorities’ just published assumptive baloney which conformed to a narrative that suited the centralized elite and their paradigms, with no medical evidence behind it whatsoever……Then why would any sane person contend, ‘Trust the Science’?

If you don’t treat someone, until they are almost dead – your treatments aren’t going to appear very effective when the studies are published.  This is how the methodology can be used to skew the truth.  This creates an opportunity for the political ruling class.  Then you can use that data, to cite that treatments are ineffective – so there are none.  This can be used to create legal means to create a solution via a patent that has legal protection.  This is how the EUA idea was born by Big Pharma during Operation Warp Speed.  This is why Hydroxychloroquine and Ivermectin were vilified in 2021.

In fact, I will take this idea further.  I now believe they all believe that natural immunity is viewed as an illegal theft of pharmaceutical intellectual property by people in power.  They believe COVID was a flu that accidentally blew into your lungs or gut.  Your immune system then attempted to usurp Big Pharma IP.  Your thieving-ass immune system was and remains their real enemy. That is how centralized healthcare operates now.  This is how centralized medical systems think. It is also what the people who sit next to its money printer think. This is how the Cantillon effect operates in medicine now.  This is why most physicians follow the mandates of those who pay their salaries.  It is also why hospitals now employ most physicians.  It is done by design to gain control and compliance to their beliefs.  Physicians no longer work for themselves.  They work for centralized healthcare systems.  If you take money blowing downwind of a bank robbery, you’ll see another centralized system that will force you to pay it back.

The moment you allow the government to break the law for an emergency, you will live in a daisy chain of emergency from that day forward.  That is centralized healthcare in a nutshell.  

Any power taken by the government without constraint leads to abuse. Remember when ‘two more weeks’ and ‘flatten the curve’ was a thing?

It was only 50 political narrative shifts ago.

COVID was a crisis ( a compliance test) that was used to make way for the most extreme and widespread suspension of constitutional freedoms in American history, despite being based on myths and lies.  The goal of these maneuvers was to replace the US constitution with the UN Charter.  This would remove your inalienable rights and put the government’s interest in front of your own.  That is why the global elites have infiltrated political cabinets all over the world and that includes the USA.  It is what they have been doing since World War 2.

SUMMARY

From the beginning of the Coronavirus crisis, the media and politicians engaged in myths, half-truths, and even flat-out lies to bring about obedience from the populace.

COVID was built as a crisis by politicians to create a cultural war to divide us so they could conquer us.  It allowed a deep dive into how those in power used the emergency to consolidate power and change the very concept of American freedoms. The government, media, advertisers, and scientists all sought to set an agenda to strip Americans of their rights. From church attendance to running a business, right down to how many people can be in a private home, few rights were left wholly unchecked. What’s worse is that any challenge to the holy laws of lockdowns was criticized and censored as dangerous and deadly speech. The question that remains is whether Americans will ever allow centralized systems to destroy their lives again.

When you see all the data flowing in regarding “Died Suddenly”….do you ask yourself if maybe   Common sense died suddenly first….  or   Critical thinking died suddenly…..after being injected by propaganda?

The centralized paradigm thinks biology is driven by a DNA paradigm.  Decentralized medicine is driven by the other genome, the mitochondrial genome that responds to the thermodynamic situation of the environment.

I have chosen the team I play on.  It is up to you to decided your team.

DUE DILIGENCE OF YOUR CHOICE

Modern epidemics are not caused by genetics, but by epigenetics!

This is also a clinical medical fact that gets lost in the modern scientific literature but you would never get that from reading the literature on diabetes or any other neolithic disease. In fact the totality of the diabetes literature would have you believe the exact opposite. This is a centralized neolithic thought that has harmed all modern diabetics and is at the seat of why modern medicine has failed to find a cure.

Mother Nature has a cure for insulin resistance in all eutherian mammals. That answer is thermodynamic.  It is mitochondrial based and has nothing to do with defective RNA/DNA.  Your choice need to change so that they marry strong solar power with night time cooling by avoiding all heating and lighting at dark.  Nature & decentralized medicine is non negiotiable with this prescription.

That is cold exposure of there peripheral nervous systems, is critical in informing the brain what probabilities should happen at night.  Artificial light at night changes the probabilities when a human makes the wrong choice.

The stimulus to this pathway begins when the mammal is exposed to a high dietary carbohydrate diet that is found in long light cycles on this planet.  It is magnified at higher latitudes.  It is minimized at the equator.  The truth is found in mitochondria haplotypes. The electromagnetic signal of Earth informs the cell that the membranes need to adapt to cooler temperatures.  This is why certain haplotypes exist in different latitudes.

This is how the gut senses the environment and this signals are transmitted to the brain via the vagus nerve. Centralized healthcare & modern biochemistry books and biochemists stop here at this level of understanding.  YOU MUST GO FURTHER.

Their beliefs are built by what THEY believe they know about energy transformation in cells. But I always focus in on what they have failed to realize.

When dietary carbohydrates are high it stimulates the eutherian mammal to begin to upregulate omega 6 content into every cell membrane of their body slowly through the autumn while temperature falls. It speeds up as the temperature drops in winter. This process is completely independent of dietary sources as I laid out in the Cold Thermogenesis #3 blog.

Why does this occur in all mammals?

People forget that lipid membranes are objects in cells that are very sensitive to electromagnetic signals.  The proof is found in how membranes are built and vary via temperature variation. For example, in mammalian cells, the plasma membrane cytoplasmic leaflet usually contains more phosphatidylethanolamine (PE) and phosphatidylserine (PS) when compared with the outer leaflet rich in sphingolipids.  There is an electromagnetic reason for this.  The phosphate groups in membrane phospholipids bind strongly to water because they are hydrogen (proton acceptors).  This singular fact suggests that light signals activate the membranes.  The membrane alters the hydration and dehydration of proteins and metabolites and in turn are critically important in activation control and deactivation of all the biochemical pathways in cells.  These are choices made by light and temperature variation.  That is why crcadian biology is the key to recapturing your health.

Maintenance of membrane fluidity by DHA incorporation, despite the presence of saturated lipids, is sustained by integrated sterols that interfere with acyl chain packing.  This mixture changes its electrical conductance and impedience.  Membranes vary the reactivity to light.  It is like cells can change the semiconductors they use as seasons change.  Those changes are signaled to water below the cell level. Conversely, because sterols themselves are inflexible they can increase membrane rigidity if associated with flexible unsaturated lipid bilayer. It is worth noting that cholesterol deposition can similarly be asymmetrical and differs greatly among organelles and in tissues in mammals.  Mammals are highly adaptable to environmental variation.

Because to cell membranes to function in cold weather it requires all land based mammals from cold adapted ancestors to have an EFA ratio of 4:1 for optimal signaling. In water based mammals who are cold adapted, like whales, walrus, and seals, humans they face steeper temperature gradients in the water that require a much lower EFA ratio (essential fatty acids) in their cell membranes to function properly.  Water transmits heat changes 24 times faster than air does.  This is why temperature variation matters in decentralized prescriptions of disease reversal.  To see this effect look at what heavy use of the AC power grid did in Spain to annual birth rhythms of humans.  Does this look like the scientific reason of what happened in John Calhoun’s Universe 25 experiments done in labs over and over again?

This lowered ratio of EFAs also changes the biology of adipocyte biochemistry below the skin level where light enters the body. It favors the accumulation of surface fat but not of visceral fat. Visceral fat is used to burn first to maintain core temperature in these animals. In land based cold adapted mammals like the polar bear the same is true. When they emerge from their den in spring they are shredded of all visceral fat and no longer insulin resistant, and have the biggest and strongest muscles they will have all year. Their body composition is at its best at this time. They accomplish all this without needing any exercise to do it.  Do polar bears or any other animal but humans have indoor lit gyms?

This is in counter distinction to modern man beliefs. Why is this? The question is more complicated than the answer, but the answer is again, simple.  It is simple because it is based in decentralized wisdom.  Light and dark control the circadian mechanism.

Modern man is further down the evolutionary path because its optical lattice clock in the eye is best atomic clock on the planet.  Everything should be thought of clock.  Humans have the most accurate timepiece of any mammal on Earth.  But its accuracy is ruined when its periodicity of light and dark is disrupted.  Better clocks mean it can support a faster evolution.  Fast evolution has another name.  It is called epigenetics.  In offspring it is called transgenerational epigenetics.

This implies in mammals, after the KT event, evolutionary development was the product of a sped up epigenetic process. Photosynthesis was disrupted.  The next generation of mammals had to quickly adapt so they could navigate this changing environment.  Life faced this before at the Cambrian explosion as I showed in my Vermont 2019 talk.  The sun changed 650 million years ago before complex life forms showed up on Earth.  Light sculpts all life.  It is not arguable any longer.

The rapid changes in the environment had to be transmited to the next generation to guarrantee survival.  The reason was due to massive environmental changes that occured due to the dsruption of photosynthesis of the KT event.

The KT event subtracted UV light from the thermodynamics of life.

This made the environment colder at most latitudes for many years after the event.  In essence, the electromagnetic response of complex cells to an extinction level event was to speed up epigenetics over time.  This wass a complex thermodynamic response to a lack of sunlight.  This negative, set the tone for future human evolution.  These environmental actions 65 million years ago allowed for the human brain to develop faster 2.5 million years ago because cellular machinery us were adapted in our epigenetic tool box to build a more complex body plan when the sun returned for mammals.  It advanced epigenetic evolution because he sun returned with photosynthesis yield post KT event.

With photosynthesis back our diet once again became an electromagnetic bar code for latitude and tectonic plate motions.  The return of UV light gave us a new way to deplete deuterium further because of the epigenetic changes that caused our mammalian mitochondria to become efficient at depleting it from foods.  UV light is critical in depleting deuterium in mammalian cells.  Look at the absorption spectra of proteins compared to the electromagnetic spectrum of light.

This allowed our cell membranes to signal both electric and magnetic field strength to the interior of cells where our mitochondrial reside.  As a result, our diet radical changed again from our immediate ancestors, the chimpanzee.

This ability caused two simultaneous evolutionary adaptations to occur simultaneously. As our brain expanded, our guts shrunk in length. We only needed a smaller gut when we become adapted to eat predominantly fat and protein from marine animals.  This diet built a faster clock because of the effect of DHA on the central retinal pathways.  This made our eye clock wildly sensitive to changes in environmental light.  This was a benefit that drove hominid evolution but now it has become our major weakness as a species.

Man made light destroys mitochondrial redox by lowering cell voltages on the inner mitochondrial membrane.

After the KT event, our SCN became a better optical lattice clock with the return of full powered terrestrial sunlight.   A diet high in fat and protein was also used to fuel encephalization of hominids. DHA in the marine chain was critical in this change.  Larger brains meant we needed pelvic changes to become bipedal and it also extinguished the need to hibernate. Hibernation needs were shrunk from seasonal changes into our sleep cycle during stage 3 and 4 sleep. As we became smarter (DHA infusions in eye and frontal lobes) we became able to not only react better to electromagnetic signals in our environment, but we became able to control our environment. We changed light in our environment because of how our brain adapted.  This is how a sped up epigenetic plan set up modern man to become more susceptible to many biochemical mismatches.

SUMMARY

When our recent ancestors lost the ability to hibernate, they also lost their best way to fight insulin resistance. Since those ancestor mammals ate carbohydrates in a proper circadian cycles, purely controlled by their seasonal growth, the biochemical systems in those mammals readily adapted to these new states without much problem. This biologic adaptation required alteration of the leptin receptor to function with higher levels of cytokines present. It appears natural selection also made adjustments to liver biochemistry and bioenergergenics to mirror those changes made in the brain.

Every eutherian mammal born on this planet up until 2.5 million years ago had to live by the dictums of their environment. When hominids evolved, much later, this environmental situation radically was altered. Hominids remain the only mammal on the planet who can 100% control its own environment. This allows our species to create mismatches at even a  great speed, as our brain continued to develop over the last 2.5 million years. This trend dramatically speeds up all our chemical clocks in every cell of our body that is controlled by circadian biology. This is well known by modern science, but its implications are IGNORED.

The Nobel Prize of 2009 tied this all to telomere lengths in our cells. The 2017 Nobel was given for circadian biology.  It is time you all pressure centralized healthcare to begin working for you and how biology works and stop supporting centralized healthcare that works for Big Pharma and Big Food.

All mammals have circadian signaling hardware in their brains that wire directly to the cell cycle machinery in every single cell of their bodies. This means that modern hominids are the most sensitive mammal to any circadian mismatch compared to their ancestors. Moreover, since they have the most advanced brain in the mammalian family, they are subjected to the greatest risk of neolithic diseases due to these mismatches. Humans get diseases that no other wild animal gets for this reason. Humans get autoimmune disease when our most recent ancestors, the chimp can not. They do not have zonulin and we do. This is one of the most fundamental reasons why our guts are adapted to different diets that lead to our encephalization. Animals domesticated by humans suffer the same fates as we do, ironically. Wild mammals tend not to get these issues because they live by the rule that Mother Nature determines for them in their own selected environments.

The ultimate paradox of modern hominids is that they evolved the ability to live on a warm adapted diet and in a warm environment, but that they retain the cold adapted biochemistry buried in their brains even though they do not need to use it presently. Evolution has not extinguished this ability for a very good reason, in my view. Mammals survived an extinction event because of it.  One reason is that the geologic record shows that our planet undergoes cyclic cooling and warming over longer epochs. This will keep the pathway active epigenetically over thousands of years.

The main reason it has not been extinguished in my opinion, is that this ancient pathway determines ultimate survival of the mammalian species and it was vital at one time in evolutionary history. Modern hominids have an advanced nervous system, but they still are tied to the evolutionary family they came from long ago. They are not divorced from the rules of Mother Nature even though they act as if they are. This ties modern humans directly back to Factor X at the KT event. The paradox of this situation is that they remain blind to it even today.

CITES

1.  https://pubmed.ncbi.nlm.nih.gov/12562849/

2. From the file of they are waking up to my perspective:  Circadian disruption and human health: A bidirectional relationship – Abbott – – European Journal of Neuroscience – Wiley Online Library.  https://onlinelibrary.wiley.com/doi/10.1111/ejn.14298

Listening well is often the only thing needed to really help someone. No one is as deaf as the centralized man who will not listen.  You earn the right to be heard by listening to others first.  Do it carefully to understand how they think before you respond. Most folks do not listen with the intent to understand; they listen with the intent to reply.  Seek to understand a situation before judging its faults or merits.  Listen to your elder’s advice carefully. The wise do this not because they are always correct about things, but because they have more experience of being wrong.  The smartest among us always learn to avoid the pitfalls of life with via the experience of others who made the errors.  Our mode of thinking sculpts our perspective. We only see what we think about because it forms how we choose to see the world.  This is why listening is a tool of the wise.  You can dissect anyone or thing when you learn how to listen to how someone thinks.

Good circadian clock management creates lives with less volume creation and more storage at night for urine. Nature seems to want diurnal mammals to drink water prior to sleep.  The system is built for this type of behavior.  All neurons move and release water when neurons fire action potentials. Thirst is controlled by posterior pituitary vasopressin.  Vasopressin is directly acted upon by light coming in through the central retinal pathways to affect the posterior pituitary.  The posterior pituitary output affects the immune system’s ability to function.  The nervous and immune systems are engaged in bidirectional communication as the picture shows.  Vasopressin is a big part of this blueprint.

I believe all autoimmune diseases are related to the disruption of the bi-directional reflex loops you see in the pictures above.  I believe the damage begins with light we are not built for.

T-Cells are the key player in autoimmune conditions. We’ve known this since 2003. In 2016 we found out how blue light causes T-cell motility. We now have all the pieces to explain the basic mechanism of all autoimmune diseases and why it is linked to the blue hazard.  HYPERLINK

Autoreactive T lymphocytes are key players in autoimmune diseases. They can act both as regulatory and effector cells. Various animal models have been used in the literature to show that the transfer of autoreactive T cells is sufficient to induce a model of an autoimmune disease. Thus, the pathogenic importance of autoreactive T cells has been formally demonstrated in animals. This should inform centralized healthcare that autoimmunity is tied to our light choices but patients never get told this.

Robert O. Becker taught us that injured tissue elicited an electromagnetic signal to begin wound repair. He found that an electrostatic field, negative away from the limb stump, could enable the regeneration of a frog limb.  Becker ascribed regeneration capability to the existence of a nucleus in the salamander’s erythrocyte. (The mature erythrocytes of frogs and higher animals lacked a nucleus.) Erythrocytes with nuclei seemed to have the dedifferentiation capability required for later differentiating into the various cell types needed in the growth area. Becker described these studies in his 1985 book The Body Electric, and also (condensed and compared with other fields) in the first part of his 1990 book Cross Currents.

The video above also shows this effect in the animal modeling of human cell injury in trauma.

Vasopressin (AVP) is released after every type of brain injury.  All injuries cause an electromagnetic stimulus to direct repair, as Becker found in his work.  This tells us vasopressin responds to electromagnetic stimuli even outside its normal circadian cycle.  Non-terrestrial forms of light is a light stress.  It is a form of traumatic brain injury.  Light injuries have become the most common non-military injury humans get in the modern world in their neurons.

Normally vasopressin is released at night when light is not present.  Artificial light post-sunset causes massive early chronic release of vasopressin.  Screen time during the day exacerbates this.  I believe that this is critical in the development of diseases like Multiple Sclerosis.  Research has shown that people with MS respond to vasopressin antagonist drugs to heal their myelin deficits.  This tells clinicians that the chronic release of vasopressin to light stress is the key problem in this immune-mediated disease.

https://twitter.com/DrJackKruse/status/1609921221017190407

Is Nature’s clue found in vasopressin molecular structure?  They are.  Vasopressin is a posterior pituitary hormone which means it has a direct connection to the retina and the SCN.  It also is directly related to the neuroimmune system.  It tells us sunlight is the electromagnetic stimulus that vasopressin reacts to.  Vasopressin is made in an area with no blood-brain barrier telling us that it is open to the environment’s electromagnetic signal.  Vasopressin is made of 9 amino acids.  The amino acid sequence of arginine vasopressin (argipressin) is Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2, with the cysteine residues forming a disulfide bond and the C-terminus of the sequence converted to a primary amide. It has two clues it is a circadian qubit.  It contains two aromatic amino acids and it has a disulfide bond linked to its cysteine residue (re-read the orexin blog to understand the importance).

Mother Nature seems to want enough water in the system for the neurons in our brain to be able to anticipate it can follow the circadian rhythm of CSF production for the brain’s glymphatic system, and that there will be enough to not compromise autophagy.

One of his key goals is to design a sensitive vasopressin test for healthcare workers to use for people with circadian arrhythmia in the Emergency Room. If levels could be assessed rapidly, it could help physicians to understand how the body is managing water, giving clues as to how to deal with various illnesses with blue light and nnEMF exposures.  In experimental models of cardiac arrest, vasopressin increases blood flow to the heart and brain and improves long-term survival.  But vasopressin release in excess seems to be one of the things that cause chronic injury to myelin in Multiple sclerosis.  This is why Big Pharma is developing vasopressin antagonists drugs to treat it.

Why? Our modern lights dehydrate us causing us to age faster and die sooner.  Sunlight hydrates our cells.

Middle-age serum sodium >142 mmol/l is associated with a 39% increased risk of developing chronic diseases  & >144 mmol/l with a 21% elevated risk of premature mortality. People with serum sodium >142 mmol/l had up to 50% higher odds to be older than their chronological age.  High serum Na is a proxy for your Light clock management behavior at the SCN level.

Until recently (2017), it was thought to only work in a classic, negative feedback loop: when we are dehydrated (bad matrix function at CCO), levels of vasopressin rise, which causes urine to become concentrated in the kidneys, freeing up more water to be used in the body.

Conversely, when we have too much water in our body, vasopressin levels decrease, and urine is diluted. What if that is not all that vasopressin does?

Vasopressin changes the possibilities that water presents to the quantum programs that control wound healing by altering charge density in coherent domains of water.  This adaptation is done by altering the epigenetic programs in cells.

Water is the quantum stage cells play on.  Water is created by cytochrome c oxidase in the mitochondria.  The spinning Fo head of the ATPase sits adjacent to the CCO. That spinning Fo head creates a magnetic field at the subatomic level. Inside a cell, water also has a magnetic dipole effect (negative and positive ends) because of the hydrogen and oxygen that make water up.

Hydrogen is positively charged, and oxygen is negatively charged. This creates a bar magnet effect in cells. These physical features are what help water networks respond to electromagnetism and waves of light.  If you look at the vasopressin molecular structure above you’ll notice on one side of the disulfide bond there are a lot more negatively charged oxygen atoms.  This tips the magnetic flux one way to signal wounds should heal using the epigenetic programs mentioned in the video above and found in Becker’s books.

I believe vasopressin is a highly negatively charged protein that is a qubit for the quantum brain that changes epigenetic signaling in tissues.  Vasopressin is how we influence probabilities of future events in water using sunlight as a lever.  

It seems organisms use vasopressin levels to predict and prepare themselves in advance for environmental changes that have selective advantages over those who cannot accommodate themselves until the changes of the environment have taken place to cause dehydration of mitochondria for some reason.  ALAN causes massive dehydration in the mitochondrial matrix.  Doing this long-term will shorten longevity by leading to diseases like MS.

In 2017 the same researchers found vasopressin does a lot more than they thought initially. They found that not only is there a vasopressin circadian feedback loop, but “it’s also involved in feed-forward mechanisms. This is quite important in understanding from a chronobiologic perspective. They determined that this molecule is produced in the brain right before people go to bed WHEN IT IS SUPPOSED TO BE DARK, and during sleep, in anticipation of the dehydrating effect of sleep. During sleep, autophagy is supposed to be very active if you are healthy.  Vasopressin is normally released at 9 PM.  It is designed to offset the dehydrating effect of sleep.  Vasopressin is also known as an anti-diuresis hormone.

I believe vasopressin induces a negative magnetization in water networks.  What is negative magnetization?

When negative charges are added, we can find a temperature-dependent crossover of the DC magnetization from a positive value to a negative value of a material (cooled under a positive applied magnetic field) is termed the magnetization reversal or negative magnetization.  Becker found this flip in the DC magnetic field between sleep and wakefulness and between consciousness and general anesthesia.  Vasopressin helps us sleep when water creation is reduced.

Moreover, when you are recycling mitochondria during autophagy you cannot make any water at CCO. What happens if you cannot make water even in the sunlight because you’ve lost total control of autophagy because of chronic toxic blue light and nnEMF light stress?

The core skill of a successful Mitochondriac is error recovery in Nature, not failure avoidance from prior poor decisions.

There is only one way to repair that well. It means that we need SUNLIGHT IS MANDATORY to make water at CCO during the day. If you do not get enough or live at a high latitude and inside you need more water. If we do not get enough sunlight then we lose circadian feedback control of vasopressin and the entire water cycle in our body.  This is how lousy clock management leads to epigenetic disease by decreasing mitochondrial redox power.  You saw this in the petri dish picture above in the video.  A loss of redox power = disease state or injury state.

So people who are incentivized by selling DDW need to be vetted.  They have not thought this out well from the Black Swan mitochondria perspective.

Our light choices can be seen in our labs if you know what to look for.  Our light environment trumps chronological age as an epigenetic driver.
Frequent shift work results in more urination for ANY AGE because the circadian gene Rev-Erbα controls the production of Cx43, which determines how much urine a bladder holds.

TL;DR: Poor circadian rhythm = More urination = more disease = FASTER DEATH COMES = THE RELATIVITY OF TIME MODELED.

Energy and light frequencies are the only predeterminants nature needs to change water’s behavior in your cells. 

As the environment’s frequencies and power density change so do the reaction of water in you. When you begin to realize how sunlight changes in different latitudes on Earth and in different cities because of 1G-5G footprints it should begin to make sense to you why you perform differently in differing locations. Water is made at cytochrome 4 called CCO. What if that process is disrupted by the environment? Is the fidelity of the signal destroyed? Will the oscillation pattern of the inner mitochondrial membrane also change? Is this why we lose the ability to fat burn with the 100Hz oscillation needed for beta-oxidation in alien environments?

If so, does this affect how much water is made and how that water reacts within the metabolic cycles of the cell? You bet your ass it does. This is how nnEMF is operating to make you ill way below your ability to perceive it.

SUMMARY

I have found in my “internet guru career” those who are easily shocked about things or words I utter should be shocked more often in their life. This is why our brightest blazes of insight in life are really kindled by unexpected sparks of insight. Be unique and light people up because you are extraordinary in how you think.

Is drinking water post-sunset mandatory for outdoor living creatures based on what we’ve discussed here?   When humans tell you not to drink water might they be incentivized in trying to sell that belief (Boros and his DDW krewe in LA)

Canadian research showed that mammals tend to increase water intake just before sleep when sunlight is absent. Rather than being motivated by a physiological need for water, the drinking response was solely based on the animal’s circadian rhythms.  The efficiency of your circadian mechanism is critical to this mechanism working as it is designed.  Sunlight creates water, darkness doesn’t <———-BIG FREAKING DEAL ALERT.

When a cell is de-polarized it is deformed by water, and potassium is released. This normally causes a glial cell to swell. This causes a volume change in the adjacent neuron (astrocytes).

When water moves, it changes the refractive index of bulk water in the extracellular compartment of the neuron to create a large coherent domain of water within the neuron and below the myelin level. The astrocytes work as a giant drainage system for water, which uptakes potassium ions in regions with high potassium, and sends them to regions of lower potassium ion concentrations. Vasopressin changes how the drainage system operates.

Vasopressin or antidiuretic hormone, which is made in the posterior pituitary gland, allows the brain controls the flow of water to activate itself in accordance with the stimuli that it currently faces. Any trauma to neurons causes its release. Normally vasopressin is controlled by circadian stimuli. The sun normally controls the release. Artificial light is a light stressor. It causes the release of vasopressin outside of the circadian mechanism.

Fact: Blue light/nnEMF dehydrates cells because they stop H2O production from the mitochondrial TCA cycle. Why is this a big deal? Neurons absorb and release water when firing information via their action potentials. When H2O is missing in action so are neurological functions/capabilities. Check the link here.

Bai, Ruiliang. Brain-active transmembrane water cycling measured by MR is associated with neuronal activity. Magnetic Resonance in Medicine. https://doi.org/10.1002/mrm.27473

The gist of this paper is that neurons absorb and release water when they relay messages throughout the brain and peripheral nervous system. Tracking this water movement with imaging technology may one day provide valuable information on normal brain activity, as well as how injury or disease affects brain function. 

The study appeared in Magnetic Resonance in Medicine.  Just how devasting is artificial light on water flowing in neurons?  4% of the world has autoimmune diseases related to the blue light hazard.  There are just over 100 human autoimmune diseases that afflict humans. 

Current functional magnetic resonance imaging (fMRI) technologies measure neuronal activity indirectly by tracking changes in blood flow and blood oxygen levels. Neurons communicate with each other by a process known as firing. In this process, they emit a slight electrical charge as an enzyme moves positively charged molecules — potassium and sodium ions — through the cell membrane. In the study, when researchers stimulated cell cultures of neurons to fire, they found that the exchanges of potassium and sodium ions were accompanied by an increase in the number of water molecules moving into and out of the cell.

Water movements only occur in the CNS/PNS via water channels that are made up of aquaporin 4 gates. This is going to become important later in the explanation of various diseases (MS). EVERY brain disease and EVERY autoimmune disease is tied to malfunctions in this mechanism

Remember that when water leaves a neuron, it carries a larger negative charge, and this charge induces an increase in the coherent domains in water networks inside the cytoplasm of the neuron. When the size of the coherent domains increases, it increases the optical efficiency within the neuron and outside the axon beneath the myelin where the interfacial water resides.

Remember that it is this interfacial water where Robert Becker found the regenerative DC current. This is why circadian biology and sleep are directly linked to regeneration. It all has to do with the scattering of light in water in neurons.

Ask yourself this: Is it biologically possible to predict the effects of lifetime exposure to electromagnetic, chemical, and physical agents that are not part of the biological experience of man given what we know about the butterfly effect?

If you do not fully understand light will you ever come to realize how important water is to life?

Evidence-based science has divorced itself from nature’s evidence.

Quantitative evidence-based science is used to remove uncertainty by transforming it into a probability for algorithms so that mathematical modeling can play the ritual role of haruspices. This epistemic governance arrangement in science is today in crisis.
The primacy of science today is to adjudicate political issues and it is having massive collateral butterfly effects on public health.
They must pass through an assessment of the level of maturity and effectiveness of the various disciplines deployed. The solution implies abandoning dreams of prediction, control, and optimization obtained by relying on a limited set of simplified narratives that linear thinking scientists and clinicians can understand to define the problem and moving instead to an open exploration of a broader set of plausible and relevant stories that define the real issues at hand.

CITES

Mae-Wan Ho, Fritz Albert Popp, Ulrich Warnke Bioelectrodynamics and biocommunication 1994, p. 21

https://medicalxpress.com/news/2023-01-good-hydration-linked-healthy-aging.html

https://medicalxpress.com/news/2019-03-younger-nightshift-workers-shown-pee.html

https://www.nature.com/articles/nature19756

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400257/

http://www.photonics.com/Article.aspx?AID=41237

Are assumptions the mother of all fuck ups?   Some will try to convince you that your assumptions are your windows to the world. They’ll tell you to scrub them off every once in a while, or the sunlight won’t come in to inform you of the truth.

Assumptions can be dangerous things for people to make, and like all dangerous things that are made — bombs, for instance, or strawberry shortcake — if you make even the smallest mistake you can find yourself in terrible trouble because of the consequences. Making assumptions simply means believing things are a certain way with little or no evidence that shows you are correct.  Moreover, if you just think about how assumptions affect thinking and decision-making, you might be able to see how this can lead to terrible problems. For instance, one morning you might wake up and make the assumption that your bed was in the same place that it always was, even though you would have no real evidence that this was so, that it had floated out to sea, and now you would be in terrible trouble all because of the incorrect assumption that you’d made. You might be able to see now that it is better not to make too many assumptions, particularly in the morning when the sunlight rises to inform you by uploading her wisdom.

On the other hand, assumptions can be useful.  Assumptions could be used as an artist’s palette of paint, and when we slept in that bed on a plane we’d use our beliefs to paint a new masterpiece as well on a freshly stretched canvas.  Your mind would act the role of the brush that pushes the paint around the canvas’s surface as you dream and assume what awaits you in the City of Lights.

Here, an assumption might look like this:  When you got out of your bed this time, you might discover that the bed was in a plane.  When you went to sleep you were flying over New York from Chicago on your way to Paris for the holidays just to be seduced by the lights, music, and atmosphere.  You wanted to dance the Tango on the Seine.  Below Point Neuf, you’d planned to meet a vivacious Frenchwoman who would invite you to a dark fire-lit jazz joint in Monmarte.  There you’d look into the eyes each other over a glass of Bordeaux.  Then, you’d get invited to her rooftop terrace where you’d gaze at the Eiffel Tower under starlight while resting your head on her beautiful shoulder.  Then, you’d wake up in white satin sheets and have breakfast in bed waiting for the sun to rise.  Then you’d walk hand in hand over to Point des Arts to hang up our lovelock.  But just then reality woke you in the bed of the plane over an ocean and you’d realize you never really appreciated what your job was really about.  You take people to places they dream of going by giving them a new chance to assume and choose.  Choices really are the hinges of destiny in life.  When you woke up and stepped out of that bed on the plane you’d realize you were traveling into a new world.  A superposition of what might be.  Here, one can be met by unfamiliar scents, where the colors of the rainbow take on a different filter, and where hearts can acquire a new beat.  You’d begin to realize you are so glad you are who you are, rational, calm, and so determined because the world needs people like you to get people like those reading this, to a place they have trouble imagining.

SUMMARY

Your perceptions influence all areas of life. The totality of your perceptions— regarding yourself, your life, life in general, and others, creates and impacts your personal reality and ultimately your experience of life.

Negative, disabling assumptions lead you in the direction of a very dismal reality. Positive, empowering assumptions give you every opportunity to live a rich, fulfilling life. Though assumptions don’t make your wishes come true, they can give you the perspective necessary for bringing your dreams to life.

Perception acts as a lens through which we view reality. Our perceptions influence how we focus on, process, remember, interpret, understand, synthesize, decide about, and act on reality. In doing so, our tendency is to assume that how we perceive reality is an accurate representation of what reality truly is.  Through perception, we become more aware of and can respond to our environment. We use perception in communication to identify how our loved ones may feel. We use perception in behavior to decide what we think about individuals and groups.

Perception is everything; the way you perceive things, the way you see things, is ultimately the way things will play out in your life.  Perspective helps us to understand situations from other positions and to consider other beliefs, experiences, and viewpoints. This gives us a better understanding and greater empathy. It reduces bias, and judgment, and reduces conflict.

The power of perspective is an intentional discipline. It takes time and commitment, but it creates an understanding between you and the people you lead that allows you to move forward, faster—and with increasing success.

Your perceptions need to be sharpened in 2023.  Realize you need to describe your relationship with truth and false perception this year.  You cannot rely on experts or the media.  You need to deal with your own and other’s perceptions.

“Perception is more important than reality. If someone perceives something to be true, it is more important than if it is in fact true. This doesn’t mean you should be duplicitous or deceitful, but don’t go out of your way to correct a false assumption if it plays to your advantage.” 

In 2023 you must obtain clarity in declaring the acceptability of what is false.