How is fear like a plague when politics gets in the way of people’s lives?

In September 1923, the Great Kanto earthquake devastated large parts of Tokyo, mostly owing to firestorms.

Rumors spread, and were often repeated in the mainstream press, accusing Koreans, a despised and poor minority, of planning to take advantage of the disaster by starting a violent rebellion. Japanese vigilantes, armed with swords, bamboo spears, and even guns, then set upon anyone who sounded or looked Korean. The media always stokes fires to grow.

Up to 6,000 people were murdered as police looked on and sometimes took part. The media was complicit in those murders, but you’ll never read that in a history book.

This was not some uniquely Japanese phenomenon. Mobs massacring unpopular minorities remain all too common. When Hindus started killing Muslims in Delhi recently, the Indian police were as passive, or as culpable, as the Japanese authorities were in 1923.

One need not go far back in European or American history to find similar, or even worse, cases of lynching and mass murder.

The medium is the message.  Social media allows everyone to be the press today, but none of them do the the bidding of ‘We The People’.  The goal of the free press by the founders was to protect the people from the tyranny of government by getting to the truth.  Content is fire today, and social media is the gas that the media is using to try to change society to an agenda their supporters want.  The media no longer is free.  They are chained to those who pay for their ads.  The INDUSTRIAL part of the industrial military complex.

CONGRESS is doing the bidding of the corrupt NAIAD/FDA/CDC by using the pandemic crisis to incite hatred.  That hatred has collateral effects that Senators and Congress people should have anticipated.  They did not.  In the beginning, those non linear collateral effects should have been considered to lead to deadly consequences.

Now they have.

Conspiracy theories can become lethal when stoked by politicians or media.  Both of stocked those fears.  

The panic that often occurs during a health crisis or in the aftermath of a natural disaster can — and has — led to spasms of irrational violence.  

Politicians will always hide behind the idea of intent, when what they should concern themselves with is the ultimate effect of their actions.  

So, as WE THE PEOPLE have seen this unfold maybe now you can see how “Antifa and Black Lives Matter” groups have gone from after thoughts to  current events.  

Who are these groups using to meet their agenda? 

Answer?  The media and  Mr. George Floyd, Mr. Jacob Blake, and Kyle Rittenhouse.  What are the facts we know at this point?    Floyd and Blake  forced his way into a woman’s home and pointed a gun at her stomach. Jacob Blake was wanted for domestic abuse and was terrorizing a woman when the cops were called. In the Me Too era it’s odd how the Left is making martyrs out of violent men who prey on women, don’t you think?

Rittenhouse was working as a lifeguard in Kenosha the day of shooting.  He went to clean vandalism at school after work.  He was not looking to kill people.  He was looking to protect his town from Black Lives Matter and Antifa terrorists.  Moreover,  The FBI has said  he did not carry his rifle across state lines.  The media has been silent on this.  The videos out there clearly show he shot two people in self defense.  That story is going uncovered by the media that supports Mr. Biden and Harris.  Have you asked yourself why this is the case?

You can’t raise money for Kyle Rittenhouse on GoFundMe — but they raised $2 million for this guy below.  You can’t defend Kyle Rittenhouse on Facebook — but you can defend this guy below

The politicians and media who let this genie out of the bottle, now can do little to contain it.  

This is why Mr. Biden and CNN’s Don Lemon are now trying to reign in looters and rioters. 

They are afraid of what pollsters are saying because their fortunes in November are now at risk.  This is the real prize for the politicians.  It is not about science or a pandemic.

We know what they are afraid of now……..and we know the cost they were willing to inflict on “WE THE PEOPLE” to get what they want…………..

 So what are you afraid of today?

For some people it’s heights. For others, it might be fear of illness or failure. For me, it’s wasting time, and people who focus on words over actions.

If you’re not running into the things that scare you, you aren’t really living, are you?

People often shy away from the things that make them nervous, because unless you’re afraid of showering, it seems a little like masochism to force yourself to face unnecessary things that can make you so unhappy. But consistently avoiding things that make us uncomfortable leaves us standing still in a world that is constantly moving. It doesn’t keep us safe; it keeps us behind the eight ball.

What is the evolutionary purpose of fear? Like GPS, our fears are our mind’s way of letting us know that we are at the edge of our comfort zone. Do you stay in that zone, or do you challenge the status quo daily?

It’s the risks we take, the times when something is hard but we march forward anyway, that adds spice to our lives and gives our memoirs the flavor a life needs.

Why should you look at your fears in the eye and smile? Nothing causes more consternation in a group of hypocrites than one honest person. Confidence is what we get when we take fear, face it, and replace it with something more useful.

“Courage is not the absence of fear; it’s having fear, but pushing through it.” This quote falls a little short of the point I want to make in this blog. This is not about supporting the left or right in this elections. Both parties are wings on the same bird. The media is mocking the bird by helping those who are abusing the people.

These ideas are not presented to sway you or scare you. They are being made to stoke your courage to speak up and no longer be silent. If you have been following my Twitter feed lately you’ll see that I am no longer remaining silent because of fear. You should chase after your fears because when your courageous act is complete, when you’ve pushed your deep-seated fears aside and chased after opportunity, at that moment you’ll truly be unstoppable.

“Nothing in life is to be feared, it is only to be understood. Now is the time to understand more, so that we may fear less.” —Marie Curie

It is time for “WE THE PEOPLE” to understand out government is at war with its people now.

Always remember: it wasn’t the rioting, looting, burned out buildings or dead bodies in the streets that made Democrats pump the brakes a little on BLM-

It was the polls finally turning against them. Nothing matters to the liberals but power. Nothing will break the left’s will to resist but another “shocking” victory in November, in my humble opinion.  Your beliefs might vary.


Did you know that melanopsin damage in the skin fat eyes or in your arteries is capable of causing anemia? How could this happen? Recent research has shown that depletion of mito-Super Oxide Dismutase, which acts as free radical in our mitochondria, inhibited succinate dehydrogenase activity leading to succinate accumulation in our colony of mitochondria. This also lowers the amount of light hydrogen isotope created from foodstuffs that is needed to reduce NAD+ to NADH at cytochrome one. The dual act seems to prevent nuclear DNA demethylation and inhibited red blood cell-like maturation from HEL cells. RBC maturation is a process dependent on DNA demethylation.

This appears how anemia of chronic disease occurs.   Anemia of chronic disease refers to having low levels of red blood cells as a result of how the presence of chronic diseases  (autoimmune diseases in which the body’s immune system attacks joints and/or body organs) or other chronic illnesses associated with low mitochondrial energy production.  People forget the first step of heme synthesis begins in the mitochondrial matrix so any level of mitochondrial damage limits heme synthesis for proteins.

Two hundred-billion red blood cells are renewed in our body every single day. These erythrocytes (also known as RBCs) are generated from bi-potent megakaryocyte-erythroid progenitor cells during a maturation process called erythropoiesis. Hypoxia stimulates erythropoiesis. Erythropoiesis is controlled very tightly and defects in the key elements of this step-wise maturation can lead to life-threatening conditions such as severe anemia or myeloproliferative disease. Transcriptional RNA interference-dependent and translational regulations are part of the core mechanisms required for proper erythropoiesis. Recently, an mRNA modification called N6-methyladenosine (m6A) has been found to control the expansion and self-renewal of hematopoietic stem cells.

In recent years, methylation at the N6 position of adenine (m6A) has gained the attention of RNA biologists because it seems control traffic in protein synthesis inside the cell. This implies that hypoxia is one of the key environmental signals to increase protein synthesis, mTOR, and uncontrolled growth in cells. The process of increased protein synthesis is controlled by the process of ubiquitination. Ubiquitination is controlled by the circadian mechanism in the human body. This links the amount of nnEMF, blue light exposure, or a lack of sun light to alterations in protein metabolism.

These are the foundational changes that support cancer generation when there is a chronic hypoxic stress stimulus.  Succinate accumulation in the TCA cycle in the mitochondrial matrix links mitochondrial MnSOD depletion to aberrant nuclear DNA methylation and these processes altered cell fates.  This is how alterations in energy production in mitochondrial causes an altered metabolism and can lead to diseases. 

Succinate accumulation is associated with increased production of reactive oxygen species (ROS) production due to an altered metabolism.  In the brain increased levels of succinate precedes neuronal injury, and plays a critical role in neurologic disease like epilepsy.  Epilepsy is also associated with hypoxia.

The production of ROS/mitochondrial ROS is associated with defects of mitochondria. For example, the production of ROS may be partly due to a defect in mitochondria that leads to altered energy consumption and energy dyshomeostasis.   There are many sources of mitochondrial ROS, including complex I (NADH dehydrogenase), complex II (succinate dehydrogenase, SDH), and complex III (coenzyme Q-cytochrome C reductase) of the electron transport chain (ETC).

Related studies have also indicated that the ROS signaling may be mainly derived from reverse electron transport (RET) to the ETC at complex I. Inhibition of complex I of the ETC induces mitochondrial ROS, oxidative damage, and increased neuronal loss

Messenger RNA is a flexible toolbox that plays a key role in the dynamic regulation of gene expression. RNA modifications variegate the message conveyed by the mRNA. Similar to DNA and histone modifications, mRNA modifications are reversible and play a key role in the regulation of molecular events.

Many people have asked me how chronic exposure to nnEMF or blue light can lead to cancer and a loss of control of this process is the answer to that question.

This is why when my members hire me to become their doctor at my Center in Destin their peripheral blood smear is one of the key things I look for that tell me about possible diseases that will be a problem for them in the future is they do not change the environments they allow.


1.       Kuppers DA, Arora S, Lim Y, Lim AR, Carter LM, Corrin PD, Plaisier CL, Basom R, Delrow JJ, Wang S, Hansen He H, Torok-Storb B, Hsieh AC, Paddison PJ. 2019. N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis. Nat Commun. 10(1):4596. doi: 10.1038/s41467-019-12518-6.

2.       Zeng et al. 2018. Refined RIP-seq protocol for epitranscriptome analysis with low input materials. PLoS Biol. 16(9):e2006092. doi: 10.1371/journal.pbio.2006092.

3.       Dominissini et al. 2012. Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq. Nature. 485(7397):201-6. doi: 10.1038/nature11112.

4.       Meyer et al. 2012 Comprehensive analysis of mRNA methylation reveals enrichment in 3′ UTRs and near stop codons. Cell. 149(7):1635-46. doi: 10.1016/j.cell.2012.05.003.

The current state of what we know about C-19 on 8/11/20

Present knowledge:  London, UK, hospital staff COVID19 antibody #seroprevalence is very high, with 34.7% for those with direct patient contact, and 22.6% for those with no patient contact. London’s general population is at 17.5%.

This is how Herd Immunity is achieved…


The higher percentages are likely due to density with high-touch high viral load, which is expected in hospitals. This is similar to what was seen in Mumbai’s slums, Australian cruises and prisons across the globe.

There is growing evidence that T-cell immunity allows populations to reach herd immunity once only 10-20% are infected with SARS-CoV-2.

This would explain why a highly transmissible virus in densely populated areas peaked at 10-20% infected regardless of lockdowns or masks.

The pervasive misconception is that we have zero immunity against COVID-19. Based on this flawed understanding, epidemiologists projected that herd immunity is not reached until 60-70% are infected.

This is almost certainly wrong.

Of course, the media ignores this research. While antibodies against COVID-19 may only last months, T cell immunity can remain protective for years.


Role of vitamin D in immunity during C19 is critical to get right.  Going outside in the sun is more wise than taking a Vitamin D pill.

A. Vitamin D is a major precursor for activation of T-cell (for any disease)

B. Vitamin D controls cytokines storm in COVID that causes blood clot & vascular damage of the organs like kidneys, heart, brain, and ultimately death.


1. Review @SpringerOpen provides detailed insight on the role of Vitamin D in building immunity by modulating monocytes, dendritic cells, T and B cells.  https://link.springer.com/chapter/10.1007/5584_2018_246

2. Scientists  @uni_copenhagen have discovered that Vitamin D is crucial to activating our immune defenses & w/out sufficient intake of the vitamin, T cells will not be able to react to and fight off serious infections in the body. LINK: https://www.sciencedaily.com/releases/2010/03/100307215534.htm

3. In this ancillary study of a randomized controlled trial, authors found that short term HIGH-dose vitamin D3 significantly reduced CD4 T-cell activation compared to low-dose vitamin D3, providing human evidence that vitamin D can influence cell-mediated immunity. LINK: https://academic.oup.com/jcem/article/101/2/533/2810779

In a study of 23 people who survived SARS in 2003, every single one had memory T cells that recognized the SARS virus 17 years later. (Nature) https://www.nature.com/articles/s41586-020-2550-z


Moreover, blood samples from all 23 individuals showed “robust cross-reactivity” against SARS-CoV-2.

This can be called crossover immunity.

Crossover immunity is not limited to just people who were infected with SARS years ago though. In the same study, in 37 persons with no history of SARS or COVID-19 (negative serology and/or samples taken before COVID-19), over 50% had SARS-CoV-2 specific T cells.

This is not surprising because there are at least 4 strains of coronaviruses that cause the “common cold”. The above study is not the only one to show this level of cross-reactivity.

In a study from April 2020, in 68 healthy donors never exposed to COVID-19, 34% had T cells that reacted to SARS-CoV-2. https://www.medrxiv.org/content/10.1101/2020.04.17.20061440v1

This finding was confirmed in yet another study published in Cell in June 2020 showing that 40-60% of unexposed individuals had T cell recognition of SARS-CoV-2.

The authors hypothesized that crossover immunity came from “common cold” coronaviruses. https://www.sciencedirect.com/science/article/pii/S0092867420306103?via%3Dihub

Crossover immunity may explain why so many young and middle-aged individuals are asymptomatic even when testing positive for coronavirus. This is why a positive test should not be alarmist with this RNA virus.

It is likely that their T cells recognized the virus and mounted an immune response before even mild symptoms surfaced. What does this mean?  This is how natural herd immunity without a vaccine occurs in Nature.  This is not a narrative that is being pushed in the media or medical circles right now.  You need to understand why.

All those runny noses from the common cold prepared our T cells to fight COVID-19.

Although it has been ominously called the “novel-coronavirus”, SARS-CoV-2 is yet another coronavirus with many similarities in structure to the common cold coronaviruses. Why are the elderly hit so hard by COVID-19 though?

Indeed the strain of coronavirus that we faced in 2020 is more lethal than those in the past, specifically in the elderly and immunocompromised…With an understanding of T cell immunity, it makes sense that the elderly are more affected by COVID-19.

It is well known that persons in advanced age and/or who are immunocompromised lose T cells. https://medicalxpress.com/news/2020-06-cell-immunity-elderly.html

Let’s get back to herd immunity via T cells.

If ~50% of people had T cell immunity prior to SARS-CoV-2, then that leaves 50% of the population susceptible.

In the regions hit hardest by COVID-19, serology studies show new cases and deaths peaked at around 10-20% infected. Adding the 50% who already had T cell immunity from common cold viruses to the newly infected 10-20% equals about 60-70% immunity.

Not coincidentally, 60-70% is the percentage epidemiologists project is necessary for herd immunity with a respiratory virus. It is likely that many of the hardest hit regions of the world (e.g. Lombardy, NYC, Madrid, London, Stockholm) are now at herd immunity.

Lockdowns & mask ordinances (mostly coming after the peak) likely had little effect, with the exception of perhaps prolonging the spread. Sweden is an example of what herd immunity looks like without lockdowns or masks.

Based on serology testing, ~20% of Stockholm was infected by April.

Deaths peaked in Sweden in April.

Today, the pandemic is over in Sweden with zero deaths per day and subsiding new infections. Lockdown advocates will challenge this thesis and point to Indian slums and areas in Peru that reached much higher infection prevalence.

However, malnourishment is rampant in these very poor regions…And it is well known that T cell function is reduced in the malnourished. This research on T cell immunity is largely being ignored by the mainstream media, possibly due to political and pharmaceutical interests.

Hint: Assuming $35 per vaccine dose (Moderna’s price), vaccinating just the USA alone will result in a revenue of ~$10 billion annually. Considering that the coronavirus vaccine industry has the potential to be the biggest profit maker big pharma has ever seen, it is not surprising that we are seeing an overly aggressive push for lockdowns and masks until there is a vaccine—no matter the cost to the public or governments.

A recent paper out in Cell needs to be highlighted.  

COVID-19, hijacks proteins in host cells that serve as master regulators of key cellular processes. These regulators are called kinases.  Sunlight has a massive effect on kinases involved with C-19 and this is why the class of viruses are considered seasonal RNA viruses.  By doing so, the virus is able to rewire the cell’s internal circuitry to promote its own spread and survival when the solar redox is poor to activate the kinase pathways in the body. But the reliance of the virus on host-cell proteins may also prove to be its Achilles’ heel, as these same proteins can be easily targeted with existing drugs that are cheap and off patent.  These are drugs that Big Pharma does not want anyone to know about because they want everyone believing the narrative the vaccine is the ONLY acceptable way out of this pandemic.


In a study published June 28, 2020, in Cell, the researchers found that when SARS-CoV-2 infects cells, it assumes control over a family of enzymes known as kinases. Under normal circumstances, kinases serve as master regulators of metabolism, growth, movement, repair and other important cellular functions. Kinases work by attaching tiny chemical tags to proteins through a process known as phosphorylation. This is how sunlight sculpts matter in your cells to alter your immunity and keep you safe.  Once attached, these tags act as switches that turn proteins on or off, which keeps the complex machinery of the cell running smoothly.

When a cell is commandeered by SARS-CoV-2, however, these same kinases behave in ways that disrupt normal cell function and transform the host cell into a virus factory. Cell division comes to a halt, inflammation pathways are activated, and the cell even begins to produce tentacle-like structures known as filopodia, which protrude from the cell’s surface and may serve as molecular highways that help the virus spread rapidly to neighboring cells.

This dependence of SARS-CoV-2 on kinases was revealed in experiments in which the researchers counted and catalogued all the proteins found in both infected and uninfected cells. Though they observed no significant differences in the total amount of protein found in each group, the scientists noticed huge disparities in phosphorylation levels – a clear sign that SARS-CoV-2 was changing kinase behavior in infected cells.

This work is being coordinated at UCSF in California. It is being done at UCSF’s Quantitative Biosciences Institute (QBI). Soon after COVID-19 emerged as a threat to global health, QBI Director Nevan Krogan, PhD, assembled a crew comprised of dozens of UCSF scientists representing a broad range of scientific disciplines in an effort to address the pandemic from as many perspectives as possible. The QBI Coronavirus Research Group (QCRG), as the cross-disciplinary team is now known, includes a number of scientists with expertise in kinases, as well as the drugs that can be used to disable them.  These drugs work against cancers.  You might be shocked to learn that hydroxychloroquine is one of these drugs.  You might begin to understand why the media and Big Pharma want to limit its use.  The media number one advertiser is Big Pharma.

For example, Dr Fauci’s NIH branch has placed a blockade in effect on Chlorquine in this cancer paper.  Ask yourself why he would do this?  Check the status on this article….EMBARGO….to be released at a later date…once you find a copy and read it….you understand why it’s been delayed….crooks against any good science that will limit the patent power for a new vaccine that Dr. Fauci and his Gates cabal will benefit from for sure.  It is a good paper to review for a Black Swan. Chloroquine (CQ) a drug closely related to hydroxychloroquine (HCQ) interfers with phosphorylation of extracellular signal-regulated kinases (ERK)1/2 and the ERK-activating kinases mitogen-activating protein/ERK kinase (MEK)1/2.  This decreases TNF which controls all the inflammatory pathways in the body that control mitochondrial autophagy.

At pharmacological concentrations,  CQ and HCQ have significant effects on tissue homeostasis, targeting diverse signaling pathways in mammalian cells. A key target pathway is autophagy, which regulates macromolecule turnover in the cell. It also recycles defective mitochondrial from direct C19 attack.  In addition to affecting cellular metabolism and bioenergetic flow equilibrium as I laid out in my July 2020 lecture here on Patreon, autophagy plays a pivotal role at the interface between inflammation and cancer progression. Chloroquines consequently have critical effects in tissue metabolic activity and importantly, in key functions of the immune system.  This is the major reason why these antibotic drugs work in viral diseases.  Dr. Fauci knew this information in 2005 as seen above.  Do you still trust the CV task force leader?



Innate cellular immunity involves nonspecific cells like Natural Killer T cells. They are activated anytime we get exposed to a viral pathogen, known to us or not. They are like a sniper that is told to kill anyone that looks like they don’t belong, as in virally infected cells. They are not specific to any virus or family of viruses.

Adaptive cellular immunity mainly involves the TNF pathways that deal with CD4 and CD8 T cells. These are produced anytime you have a particular virus. They are like a Mafia hit man who is contracted to kill someone and everyone related to that person, so a Coronavirus or any of its cousins. More specific than the NK T cells but nonspecific enough to take out infected cells of a family of viruses if the individual has good cellular immune function. They also provide longer lasting immunity than antibodies for most respiratory viruses.

The humoral immune response involves the production of antibodies (Immunoglobulins IgM, IgG) by B cells that are activated by the cellular immune response if the threat is bad enough. Think about these antibodies like an assassin with an individual target, like Jason Bourne getting a photo of his target and going after that specific person. Antibodies are like a lock and key in their response, very specific to that particular virus and even that particular strain of virus. They do not often offer cross reactive defense to other mutations or related viruses in the family.
THIS is why I have been focused on helping myself, my family, and my friends improve the innate and adaptive cellular immune response, antibodies are fine but less predictable and don’t always last for this type of virus. Also the T Cell immunity offers defense against the future viral threats that we may face, I suspect there will be more.

That is a basic immune system lesson to use when you get confused! And remember Sunlight properly shapes life and health, how’s it shaping yours?  Artificial light improperly shapes your immune system and sets your up for mitochondrial damage making a C19 infection more likely.  Is that what you want now?





Is having a relatively stable magnetic field critical maintenance of you free radical pulses at night while you sleep that helps you regenerate? This is why the magnetico sleep pad can help people when they live in an electro-polluted home or city.

Life on earth is sustained in a relatively narrow range of environmental factors and magnetic flux is one of these characteristics. Human have known about the magnetic field of the earth for several hundred years but only recently were we educated about its true complexity and how that complexity links to why humans have haplotype variation in out mitochondrial DNA.

The magnetic strength of our environment can be sensed by many animals and humans have proved this field exists by our use of specially designed instruments to measure these effects.

Earth has a varying magnetic field, is not static, but more stable under darkness when the sun is set. The poles of the planet move daily with light and dark, and their is a cyclic variation in their magnitude at a circadian rate. On larger scale magnetic poles can reverse and this has coincided with massive changes in life on Earth.

Our blood is a magnetohydrodynamic fluid that senses these changes via periredoxins. Magnetohydrodynamic factors arise in our bodies in part from the resonant cavity that formed between the Earth’s surface and the ionosphere. This cavity produces low frequency micropulsations between 0.01-20Hz but are most common at 7.83 Hz to 10 Hz. Transient solar storms alter these fields and so do lightening dischages do as well. Lightning produces RF energy in the kilocycle range which propagates along the lines of force of the magnetic field of Earth mimicking meridians on the surfaces of animals who also have their own magnetic registers due to the free radicals their mitochondria create.

As lightning bounces along these force lines between the hemisphere waves are created within the resonant cavity and they effect all living things on Earth. This occurs because the energy of the bolts of lightning is capable of ionizing atoms in that resonant cavity to affect valence electrons and often times electrons of deeper shells in atoms to change the structure of living things on Earth. Ultimately, these changes, I believe are what drive evolutionary change on Earth. As a result of these actions of magnetism, large electrical currents are generated within the Earth and the the atmosphere. The currents in the Earth are called telluric currents and the ones in the atmosphere we call the Schumann resonance.

Grounding concerns itself with telluric currents. The size and shape of the Van Allen belts above Earth have direct effects on the micropulsations of the Schumann resonance. In fact, fluctuations in the large currents flowing in the Van Allen belts is generated by the time variances found in the magnetic field on Earth. This along with the collision of the solar wind on the magnetosphere of Earth produce high magnetic currents in equatorial regions of the ionosphere which link to living things in these regions by having mitochondria which favor a tightly coupled mtDNA haplotype (L0, L1, L2, L3)

It is these magnetic currents that couple with the telluric currents in earth below that create a magnetic signature that helps format free radicals in cells using oxygen, nitrogen, and sulfur. They do this because this coupling effect results in massive DC electrical currents that discharge at the 7-10Hz frequency from the resonant cavity of the ionosphere. The discharge of these currents no only produces these micropulsations, but they create heat, UV light, and shock waves which all would have contributed to chemical reactions in living things. This is how abiotic forces affect atoms in cells to alter life.

This is why nature is counterintuitive to common sense. We are just not aware enough of how magnetic forces alter things below our ability to sense them. For example, in 1828 in Berlin humand found out that from the work of Friedrich Wohler that ammonium cyanate could be transformed into to urea by heat alone. Urea and its cycle is critical to living things. Because of magnetic forces on Earth, the heat they liberated could have taken deadly ammonium cyanate in the primitive Earth’s environment made by Ulrey like mechanisms and transformed it into a chemical life depends upon millions of years later. Heat from a magnetic transformation is capable of rearranging the atoms of a molecule into a different compound, yet still remain in possession of all the original atoms, but the new compound was something useful to the slow building up of life forms. These insights should tell you just how complex the threads of nature are when she spun out a life form on Earth.

This tells the student of life that the electromagnetic environment of the Earth is complex and diverse but operates on a direct current of electric flow. These currents are inter related to many other factors that continually vary giving living thing the opportunity to vary its form as the environmental energies vary. Our understanding of this science remains rudimentary even today.

Hardly 30 years later Friedrich Kekule in Ghent figured out how nature used methane to build hydrocarbons that could capture light to use them as chromophores. Chromophores are melatonin, T3, T4, NAD+, and leptin to name a few.

Kekule realized that benzene was a hydrocarbon that was essentially deficient in hydrogen per unit of carbon, to wit: C6H6. He realized how benzene was formed when he saw the curling of smoke emitted from his pipe and got a ‘vision” of gamboling carbon compounds on early earth atmosphere, where the crbone of methane just grabbed its own tail to create a hexagon. This simple idea changed the world. When Kekule realized that a fourth valence could be absorbed intramolecularly, the door to modern chemistry flew wide open for man. This one thought experiment is truly where Big Pharma was invented. I bet no one ever took you down this path before! He called these compounds aromatic hydrocarbons because most of them have distinct odors. They set off our sense of smell. They also are the ideal photon traps to capture different frequencies of light to tickle our retina. Nature seemed to do this experiment 4 billion years before Kekule and built life around these properties. I believe it is where our sense of smell and sight began too.

From this description above it should be obvious that man made electropollution would have an effect on these magnetic effects life depends upon. It should be obvious that things made from urea and aromatic amino acids must somehow link to how life transforms energy.

Then you should remember that tryptophan is an aromatic amino acid that forms melatonin and melatonin controls the only two change programs mitochondria use, namely autophagy and apoptosis. Now hopefully you can finally see how magnetism links to your haplotype, your melatonin levels, and free radical Rosetta blueprint.

Melatonin is made in the daylight but operates under the cover at night when MAGNETIC fields are larger than electric fields.  If you do not understand magnetism, you’ll never understand how melatonin does what it can.  It should now begin to become more clear why a magnetico pad might be able to improve your sleep.

When we sleep gas exchange changes.  As CO2 levels rise, you get less and less oxygen in each breath. This can cause you to feel sleepy, tired, or less focused because dissolved CO2 affects magnetic effects in your body.  It also cools you.  This is why body temperature changes at night and why melatonin rises as our core temps falls 2-4 degrees F to operate.

Typically, carbon dioxide levels rise during the night when people are sleeping, especially if the door and windows are closed. This is not true when they sleep outdoors.  Sleeping indoors creates pseudohypoxia.  This is where the magnetico effect helps.  Most of us sleep inside.  This creates a huge aging problem in our colony of mitochondria over time.   Unfortunately, poor air quality can hinder restful sleep and optimum health in many homes because no one engineers oxygen and CO2 levels to vary with the Earth daily magnetic fluctuations.

How does this biologic effect link to geomagnetism?

From the did you know file?  Global cooling seems to be associated with increases in geomagnetic field intensity whereas global warming is associated with decreased geomagnetic field intensity. This happens because CO2 gas solubility changes with a varying magnetic field.   Today we see evidence of decreased geomagnetic field power on Earth,  which is another factor climatologists never seem to account for a rising CO2.  Remember CO2 is also made in mitochondria from the oxidation of foods.  This magnetic effect on CO2 solubility likely plays a larger role in mitochondria than scientist thinks,  because magnetic effects are magnified at smaller scales based upon how the electromagnetic force changes strength at small scales.  Recall too that CO2 itself, can act as a free radical.   It has an unpair electron!!!

So what is CO2 up to in cells?  What is it capable of if more CO2 is buried in us when we are around alien magnetic fields from tech devices?   We cannot sleep as well, is the short answer.  This is why a magnetico pad can help with nnEMF and hypoxia at the fundamental level.

When mitochondrial oxygen consumption slows, the production of CO2 also slows and it drops.  This means CO2 levels on a chemistry 7 blood test is a great proxy for the magnetic flux present in your colony of mitochondria.  As mitochondria become less active and CO2 drops,  DNA becomes more unstable and susceptible to alien magnetic fields that can pull nucleic acids apart more easily and lead to diseases.  Low CO2 levels is something I pay attention too as we trend labs for our Farm clients.

Can a magnetico pad help hypoxia from technology because it boosts magnetic field power when we sleep on it?

Carbon dioxide interacts both with reactive nitrogen species and reactive oxygen species. In the presence of superoxide, NO reacts to form peroxynitrite that reacts with CO2 to give nitrosoperoxycarbonate. This compound rearranges to nitrocarbonate which is prone to further reactions. In an aqueous environment, the most probable reaction is hydrolysis producing carbonate and nitrate. Thus the net effect of CO2 is scavenging of peroxynitrite and prevention of nitration and oxidative damage. This is why a drop in CO2 on labs concerns me.

However, in a nonpolar environment of membranes, nitrocarbonate undergoes other reactions leading to nitration of proteins and oxidative damage. When NO reacts with oxygen in the absence of superoxide, a nitrating species N2O3 is formed. CO2 interacts with N2O3 to produce a nitrosyl compound that, under physiological pH, is hydrolyzed to nitrous and carbonic acid. In this way, CO2 also prevents nitration reactions. CO2 protects superoxide dismutase against oxidative damage induced by hydrogen peroxide. However, in this reaction carbonate radicals are formed which can propagate the oxidative damage. It was found that hypercapnia in vivo protects against the damaging effects of ischemia or hypoxia. Several mechanisms have been suggested to explain the protective role of CO2 in vivo. The most significant appears to be the stabilization of the iron-transferrin complex which prevents the involvement of iron ions in the initiation of free radical reactions.  This shields free iron from magnetic fields and limits damage.

The answer is a magnetico pad makes sense in a world filled with nnEMF as the Earth’s magnetic field strength declines.  It also makes sense if you sleep indoors chronically.

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