Blogs

 

Ya’ don’t say? Seafood, because of DHA and iodine is the key to controlling how proton spin creates a library of information for your cells. In the Brain gut blog series, I made the case, using the massive research efforts of Dr’s Cunnane, Crawford, Tobias, and Kuipers that the human brain can not function well without a diet loaded with brain-specific nutrients that favor a specific form of hydrogen to deliver energy and information to cells via the Grotthuss mechanism. This is why kids who eat seafood sleep better and have better cognition.  HYPERLINK

An increased iodine requirement as a result of significant changes in human nutrition rather than a decreased environmental iodine supply is suggested to represent the main cause of the iodine deficiency disorders (IDD). The pathomechanism proposed is based on the fact that serum concentrations of thyroid hormones, especially of triiodothyronine (T3), are dependent on the amount of dietary carbohydrate. High-carbohydrate diets are associated with significantly higher serum T3 concentrations, low Vitamin A levels, because of their links to the seasonal sun power compared with very low-carbohydrate diets. If you are paying attention, this set of circumstances, it causes pregnenolone steal syndrome to occur naturally.

This is Mother Nature’s natural “birth control” for summertime after animals have delivered their young in the spring. This reduces their sex steroid hormones on a relative basis and allows them to focus on making sure their offspring survive. UV light is well known for reducing sex steroid hormones in the blood plasma. That is how it should work when you think about nature’s plan for offspring survival……..UV light is what turns off sex steroid hormones in blood plasma when the sun is strong (June 21) Why would nature do that? Because human babies are supposed to be born during the late spring and summer and lowering the father’s testosterone level fits the plans of nature on many levels.

Sunlight increases sulfated Vitamin D3, histamine, and sulfhydryl groups while lowering the biogenic amines by photolysis such as adrenalin, steroids, testosterone, estrogen, thyroid hormone, DNA, and RNA. Sunlight induces biochemical reactions via photolysis and it induces coordinated endocrine adaptation effects in the eye and the skin surfaces by way of our blood plasma. It affects the sympathetic and parasympathetic systems. It is the stimulus for the circadian timing mechanism of the body clock via the central retinal pathways. All these effects are built into the electronics of your proteins under solar power and magnetic flux.This is why the vegan diet in modern humans is fraught with so much infertility in a blue-lit and nnEMF world. Nobody seems to make these basic links. This is why seafood is an antidote to modern technology risk factors. You have to stop listening to allopathic and functional medicine docs who tell you seafood is too toxic for any reason to eat. They do not know the science and their education of light is severely limited and lacking depth and context.

While our Paleolithic ancestors subsisted on a very low carbohydrate/high protein diet, the agricultural revolution about 10,000 years ago brought about a significant increase in dietary carbohydrate. These nutritional changes have increased T3 levels significantly while lowering Vitamin A levels. This sensitized humans to the effect of blue light because opsin biology and Vitamin A cycles are linked. Higher T3 levels are associated with an enhanced T3 production and an increased iodine requirement. The higher iodine requirement exceeds the availability of iodine from environmental sources in many regions of the world, resulting in the development of IDD

This directly implies from a physiologic standpoint, the brain specific nutrients are far more important than nutrient density recovered from a database because the hydrogen in these foods can carry more energy and information than hydrogens in higher carbohydrate foods.

CITES: 

http://www.ideafit.com/fitness-library/kids-who-eat-fish-have-higher-iq-sleep-better

https://www.jackkruse.com/hormone-cascade-101/

https://www.jackkruse.com/quantum-bio-10-hormone-102-drawn-to-light/

 

To understand many of the details in this blog you will need to see the April 2018 webinar.

IN A 5G WORLD COULD TAKING VITAMIN D3 ORALLY BE DANGEROUS?

Why shouldn’t you take oral Vitamin D3 to replace the sunlight you are not getting?  Here is the black swan mitochondriac postion because of the information quanta:  Cholesterol sulfate is also synthesized in the skin by UV light exposure of the skin…….so if you do not get the UVA and UVB light frequencies in diurnal fashion, you get lack of sulfation in the skin and blood.  This affects all things in the skin and blood.  The picture below shows the effect.

 

 

Our power grid in the USA oscillates at 60 Hz and the EU works at 50Hz. Our inner mitochondrial membrane oscillates at 100Hz when cells are using the TCA cycle. The power grid is a modulated frequency. This means that the power grid can create an interference pattern in our skin and vessels. 5G has the unique ability to jump conduct to other conductors. Your blood plasma is a magnetohydrodynamic fluid conductor. This means that atherosclerosis in young people who use technology should be expected. (below)

 

HOW DOES THIS HAPPEN? 

When the oscillation pattern is lost deuterium enters the matrix and cytosol and this is not where it should be to an excess. The normal ratio for beta-oxidation function is 6600 H+ for every one deuterium isoform. When too much deuterium enters the matrix you get energy loss as the picture on the bottom right of slide shows from Wallace.  The cristae no longer align properly when deuterium bonds to the anions of the TCA cycle. This destroys energy flux.

 

 

Energy demand shows up in the fractal organization of mitochondria. Information quanta from sunlight to H+ ions are what allows it to occur = April 2018 webinar.  What are the details of this process? 

Cholesterol sulfate (CS) plays an important role in protection from athersoclerosis, asthma, and arthritis because at the same time sunlight makes CS and Vitamin D3 it makes profilaggrin.  This last biomolecule is a prohormone protects us from asthma and arthritis.  So in a 5G world we will see massive amounts of asthma and arthritis of all forms.  UVA light also makes nitric oxide from the vessel (NO) walls and it makes carbon monooxide (CO) too from the action of heme oxygenase in the UV portion of the day.  Heme oxygenase is an enzyme that catalyzes the degradation of heme.  Notably, because of their shared reactivity for metal centers, •NO and CO share many parallel adaptive biophysical signaling roles, including stimulation of vasodilation, inhibition of mitochondrial respiration, and inhibition of apoptosis (Dulak et al., 2008). Remember, that all cancer lines need to have apoptosis inhibited to become a cancer.  This is another reason why sunlight exposure is nature’s vaccine for cancer.

Heme itself is derived from hemoglobin, myoglobin, cytochrome proteins as well as a spectrum of other proteins ubiquitous in cells.  In the skin this is a big deal because the Auger effect is used to protect us from sunburns.    This denatures DNA as skin cells die as they come to the surface.  DNA in kerotinocytes acts to absorb excessive UV light to provide a natural sunscreen in the surface skin layers.  As this happens the mitochondria of these skin cells has heme present in the cytochrome proteins, catalase, and lipid peroxides as the mitochondria parts are recycled as the skin cell die.  Heme oxygenase (HO) has been shown to be important for attenuating the overall production of ROS and decrease ELF-UV light release.

 

 

Sunlight seems to be a stimulus that helps the turnover of older RBC’s that cannot hold a photo charge as well when the arterioles come closer to the skin surface. This produces biliverdin, ferrous iron, and carbon monoxide. CO aso slows electron change transport in many tissues. We normally associate this with pathology but here you see this is normal physiology in the skin under the power of sunlight.

 

 

Local NO release lowers blood pressure and this NO can slow ECT to lower apoptosis risk to cause tissue atrophy. This protects our stem cell supply but slowing the electron flow means we do not need as much food substrate for electrons. This is why solar exposure lowers our weight. It fully explains why obesity and low Vitamin D3 levels are linked. When UVA and IR-A light are present together ECT flow slows and the ATPase spin rate can continue because cytochrome 4 has 4 red chromophores that allow the ATPase to spin with a lack of electrons. This happens because IR-A light spins the ATPase Fo head by itself to make ATP without any help from the cytochromes. In fact, IR-A light makes the ATPase a 100% nano-quantum torque engine to move protons. Red light always moves things with mass.

 

 

This explains why sulfur is a healing agent in many studies, but it is also why no one realizes we need sunlight to get it to work with all these skin pathways. Taking the supplement D3 pills don’t work, and may cause serious collateral issues. What does this mean? Like vitamin D3 sulfate, cholesterol sulfate is also water-soluble, unlike cholesterol which is not water soluble. Cholesterol sulfate does not have to be packaged up inside LDL for delivery to the tissues. Unsulfated cholesterol does. This is huge physiologic burden for liver function and why arterial disease is high in a nnEMF world.

 

 

Remember, vitamin D3 is synthesized through a couple of simple steps from cholesterol, and its chemical structure is, as a consequence, nearly identical to that of cholesterol. If cholesterol is not sulfated by sunlight than neither will Vitamin D3. I believe these sulfated things (platletss/RBC’s/heparin etc) are the key anions needed to help transfer information quanta via a subatomic proton pathway to in the blood plasma. I believe sulfation is critical to augment a version of animal photosynthesis (PS) in our blood.

The phosphorus ion is critical in this process as a ‘qubit’ with sunlight in information transfer. In plant PS it is well-known that there is a one electron redox reaction where free electrons join ADP and Pi to make ATP. No metabolic pathway is needed in this light reaction in plants. In humans we know the coherent domains in the exclusion of water create 1 million free electrons. These electrons can make ATP in the circulatory system in similar fashion.

 

 

I think sulfated D3 is what keeps inorganic Phosphorus in the blood long enough to allow the reaction to occur especially in RBC’s which have no mitochondria to make a ton of ATP via glycolysis. People forget this pathway does not make a lot of ATP but what it does make, it makes very rapidly. They rely on carbon dioxide to react with carbonic anhydrase (bicarb) via glycolysis. This is why RBC’s live as obligate glycolytic cells (Warburg like) by design to keep deuterium in the blood plasma at high levels (150ppm). This keeps the deuterium away from the mitochondrial matrix and cytosol where it wrecks havoc because of its kinetic isotope effect.

 

 

Phosphate is also a key to making hydrogen (H+) by reacting to sunlight.  Hydrogen fuel cells use this mechanism of phosphorus photosynthesis and it is well known in many industries.

What is the evidence for it?

In Japan researchers found out the phosphorus and sulfur in the proteins of chicken eggs were found to be useful in making hydrogen.  It appears animals use this as well as plants.

Here is another interesting point about sunlight that is absent with D3 pills in humans: it has been determined that the sulfated form of vitamin D3 from solar exposure is strikingly ineffective for calcium transport in humans but very critical in resorbing phosphorus at the kidney to keep inorganic phosphorus in the blood plasma.  This phosphorus than joins with the ADP of RBC’s and makes ATP in the blood when the blood is brought to the surface to be irradiated by sunlight.  What causes the arterioles to rise to the surface?  UV-A light does this with NO release.

This is why I wrote the Time 11 blog (below) about the wisdom of not taking D3 when you are deficient in D3 by blood testing.  If you do take it you are going to put a ton of calcium into your coronary arteries and your arteries all over your body over time.  (Pic below) As NO declines with age this implies one needs more sunlight not less sunlight to avoid arterial disease and blood pressure issues.

 

 

Waveform interference from 5G and the waves made in the artery by sunlight become interfered with.  This leads to the picture below due to an alteration of charge of cholesterol sulfate in arteries, the skin, and in RBC’s.  These interactions than changes how deuterium works in the plasma.  It also decreases NO release which stops the vessels from coming to surface for solar irradiation which leads to calcific plaque formation.  These plaques can crumble and fall off the wall and cause an arteriole occlusion when the frequency from the skin surface is modulated for any reason.  This will be very altered in a 5G world because of how 5G changes topology.  5G waves can jump conduct to our circulatory system.

The AC frequency in the power grid is modulated so this can be the stimulus to affect a plaque in a peripheral artery to cause blockages and heart attacks. Above, you saw an Xray of a patient of mine who was an electric powerline worker who was just 44 years old.  You can see from the picture right infront of the lumbar spine is a calcified tube running from the heart to the legs which is the aorta.  This vessel is not supposed to have any calcium in it at this age.

The collateral damage for you to realize is that in a 5G world you won’t need to be a powerline worker to get this disease because 5G can jump conduct into your body and affect your skin and arteries while you have no idea this process is ongoing.  This is why checking your body voltage may be very wise when 5G gets to your zip code.  At the same time the public will suffer from osteopenia and/or osteoporosis because the calcium is being driven into the arteries and not the bone.  Physicians will have to know to look for it because they do not understand the quantum biology of the skin with 5G.  You now know more than they do.

This is why I NEVER advocate taking calcium supplements with oral vitamin D3 because oral D3 raises serum calcium and has little effect on plasma phosphorus levels.  This creates a dangerous risk for arteries and bones.  These small details are missed by most and certainly not well-known as the “primary” role of vitamin D3.

This is why you need to vet your experts carefully in the coming 5G world.  What used to be “low risk” in a 0-4G world may no longer be safe.  

CITES:

https://www.jackkruse.com/time-10-can-you-supplement-sunlight/

https://www.ncbi.nlm.nih.gov/pubmed/21319047

https://www.japantimes.co.jp/news/2018/02/16/national/japanese-scientist-employs-egg-whites-produce-clean-energy/#.WsQ_NWaZN0s

 

Click Here to view April 2018 Webinar 

A healthy cell is unusual in that self-sacrifice is the rule in cell biology. In cancerous cells apoptosis is inhibited as a rule. What controls this process?   INFORMATION does.

Mitochondria are known to self-regulate their biology via two coupled pathways called autophagy and apoptosis. Apoptosis is self-sacrifice. All somatic cells are actually committed to die but they dedicate their existence to the survival and modification of the stem cells. Cancer cells also harvest the blood supply for its sole benefit.

AUGER EFFECT:  UV light does not break chemical bonds in DNA as the skin and eye doctors tell us. Instead, DNA is protected via the Auger effect, a process where ejected core electrons are replaced by electrons from a higher energy level, resulting in a release of energy (in this case, heat). Heat favors the formation of hydrogen bonds using H+ over D so the deuterium can be excluded by sunlight in the formation of exclusion zones to be eliminated by the body in many ways.

So this brings up an interesting angle to consider.  How does light interact with electrons precisely?  All cells release ELF-UV.  This seems queer until you understand the Auger effect.  Are their rules that govern this interaction?  Mitochondria select and order electrons and protons by spin and they transfer information to the orbital angular momentum using light waves.  Light is made of photons and photons have a quantum spin number of one.  Photons are from the family of bosons and they are the force carrier of the electromagnetic force.  So light can increase informational transfer if it can increase its orbital angular moment in some way.  How do we increase the orbital momentum of sunlight?  We can turn visible light frequencies into laser light.  Is this how it happens in life?  Yes, it is.  The fats in skin with hemoglobin and light are fully capable of making a laser light the body can use to increase the OAM or light captured inside of us.  One thing physics knows is that light seems to have an unlimited potential to carry orbital angular momenta.  This means light can carry massive amount of information but only a limited amount of energy.  The energy carrying capability is linked to the frequency of light. We now know from quantum thermodynamic experiments that information can be transferred from the quantum spin number to OAM.  This means that the spin of electrons and protons are critical to a body gaining the massive information buried in sunlight.  Now how does light interact with electrons and protons?  I have already taught you how this happens with electrons : that is the photoelectric effect.  How does it happen with protons?  H+ and deuterium have different quantum spin numbers, so they have different abilities to transfer information in light waves.  H+ can transfer more information than deuterium can.  Hence, this is another reason why H+ was selected by the ATPase in evolutionary design of cells.  The other thing to know is H+ is more lipid soluble to enter tissues that electrically active more easily.  Deuterium does not have this effect.  This means that H+ can enter tissues that are lipophilic.  It turns out human tend to bury their highest mitochondrial density in tissues that are lipophilic, namely the brain and heart.  In both organs they have the highest metabolic rate of any tissue in the human body.  I believe this is a function of their ability to have protons that can share the most information to other atoms in our cells.  Most of the tissues in our body are made of bosonic matter.  This is why I told you years ago that our tissues are a syncytium called a Bose-Einstein condensate.  It turns out those bosons in use are hungry for the information and energy that electrons and protons can provide them.  This is how life goes from abiotic to biotic in my opinion.  It is not from energy transfer.  I believe it is from massive information transfer that occurs between the quantum spin number or electrons and protons to other atoms that are organized in the zygote by the effect of deuterium.  Deuterium helps build the body plan in the zygote and helps it grow by altering mitochondrial energy and information flux tissue by tissue in amazing ways by its presence or absence at certain spots in biologic substrates.  I will have a blog this month to show you how it operates mechanistically in the retina.

How do we know how light transfers physical things like energy and information ?  We know this from the solar science done about the atomic spectra.  I told you in the first deuterium Patreon blog that deuterium is destroyed in the sun and that most of the red light in the sun comes from the H+ versions of hydrogen.  This light’s target is on all things with heme in them.  Cytochrome c oxidase has 4 of them.  That cytochrome is what controls the program of apoptosis.  This is half of the thermodynamic couple designed to get rid of poorly functioning mitochondria.  My belief is that apoptotic programs are directly related to a lack of information assimilation in the tissue in question.  I believe UV light controls the process of autophagy/mitophagy which is related to poorly functioning energy flux and slower ECT speeds are their hallmark.  These mitochondria are the ones studied by Wallace.  They have low NAD+, pseudohypoxia, higher space between the cytochromes lowering electron tunneling speeds leading to the term called heteroplasmy.  These power plants will eventually lose their ability to recycle unless UV light is restored to the system.  It has the highest energy density in the system to provide the energy flux in the system to speed up ECT flow and ROS/RNS free radical signals.  Free radicals are only produced via high energy reactions (mid-1930’s). This is likely why cells use the UV part of the spectrum to signal optically. Many of the early work on ELF-UV light showed it is only liberated when the optic heads are illuminated by light (pg 94). This links the process to my Vermont 2017 talk.

When this occurs cells begin to release ELF-UV light to the local atoms to try to make melatonin to improve mitophagy/autophagy.  ELF-UV needs oxygen radicals present to radiate light ( p.79 Van Wijk) This process can exist for a time in dysfunction but when enough information is lost with that tissue, a redox shift occurs and then the Warburg metabolism kicks in.  At this point, tissues lose the ability to recycle their mitochondria, so the only option left is to use apoptosis.  Cells and tissues “know” because of the light they contain that this is the last gasp maneuver.  But they do it waiting for the environment to return its source of energy and information from the sun.  Cells need all of the visible spectra to regain control of both autophagy and apoptosis.  They are the ultimate coupled system in a cell.  (Predator and Prey)

How does sunlight transfer energy/information?

Atomic spectra measure radiation absorbed or emitted by electrons “jumping” from one “state” to another, where a state is represented by quantum numbers with values called n, l, and m. The fourth number is S = spin.  This is the big one for this webinar.  Spin is how infromation is transferred from light to make atoms biotic.

These are called the 4 quantum numbers associated with every particle. There are quantum rules that govern these quantum transfers called the Transition rule.  I want to be clear here.  Energy and information are both transferred in packets called quanta.  Energy via the PE effect and information via quantum spin number and OAM.  It turns out OAM is another conserved property in nature, like energy and mass conservation that define the laws of thermodynamics.  Why do I mention it?  This is how life does what it does.  It appears to skirt the second law because cells are better at information transfer than they are at energy transfer.  They want to know more to become more.  They only need a baseline of energy to do this because they have perfected information transfer in their design which is codified in our RNA and DNA.

This energy and information transfer is not a continuous download. It is controlled by rules.  The so-called “Transition rule” limits what “jumps” are possible on Earth. In general, a quantum leap or “transition” is allowed only if all three numbers change simultaneously in the process.

There are exceptions to the rule is the Zeeman effect. This is because a transition will be able to cause the emission or absorption of electromagnetic radiation (photons have a spin number of 1) only if it involves a change in the electromagnetic dipole of the atom.

Why is the Zeeman effect special?  It deals with spectra of hydrogen.  Ya know where H+ and D come from?  Remember that the spinning ATPase makes a local magnetic field in the mitochondria.  This is critical for the Zeeman effect to happen.

The Zeeman Effect in hydrogen occurs when an external magnetic field is applied to hydrogen, and sharp spectral lines like the n = 3→ 2 transition of the hydrogen split seen in textbooks.  The 3 lines can be seen as multiple closely spaced lines with higher resolution.  Bohr did not have this power when he made the original of atomic theory and quantum mechanics.

This was first observed by Pieter Zeeman, when he relaized this splitting was attributed to the interaction between the magnetic field and the magnetic dipole moment associated with the orbital angular momentum in protons.

In the absence of the magnetic field, the hydrogen energies depended only upon the principal quantum number n, and the emissions tended to occur at a single wavelength.  This was easily measured with a spectroscope.

This is another reason why H+ was favored over deuterium in the quantum evolutionary construction of the matrix.  H+ has the ability to transfer more light information to them, this is how protons transfer information from the sunlight to the Bose Einstein Condensate of atoms in the rest of your body.  Sunlight animates atoms with information.  The energy flux is not the key.  The energy flux is needed to keep ECT flowing in most tissues.  You will note that not even that is needed in some tissues like RBC’s.  Why?  They have no mitochondrial so they do not use the TCA cycle.

 

 

RBC’s like deuterium and this is why our blood plasma is jammed with them (above). Deuterium and hydrogen can be used to generate ELF-UV to signal mitosis or growth in a controlled fashion when melatonin is controlling autophagy and apoptosis. When it is not deuterium can be usurped by a Warburg shift to cause cancer by liberating massive amounts of UV light from cells (Van wijk/ Popp).

How does this happen?

When deuterium or H+ have a voltage placed across them they can emit UV radiation. This becomes easier when they are under a pressure gradient. So how does this process work in you? RBC’s are loaded with Fe porphyrins called hemoglobin that acts like a dye laser. They also absorb massive amounts of light. The absobtion spectra of hemoglobin is from 250- 600 nm and the cut off is SHARP.

 

 

Since RBC are swimming in a blood which is made up of 93% water there is a ton of deuterium present. The RBC’s are light ferry and their oxygen payloads are delivered to mitochondria. The mitochondria are fed a constant source of electrons from foods or recycled FFA’s, amino acids, or glucose from gluconeogenesis. These electrons have a quantum spin that carries information of the sun when they were programmed. They are also in the excited state by the very same photons. This is done by the frequencies of light photons. This imparts a power to each electron and allows each electron to be sorted by the information and energy programs in the cytochrome proteins. The mitochondria has several dehydrogenases that pull hydrogen from foods or substrates delivered to the matrix for metabolic recycling. These hydrogens harvested from foods tend not to be deuterium because we know there is a tight specificity where deuterium is in the TCA cycle substrates as the picture below shows

 

 

The blood is a magnetohydrodynamic plasma which contains both versions of hydrogen and in many different chemicals. Most of the H+ is incorparated into hydrogen bonding networks of water and can anywhere in the body via the blood lymph or syncytium/interstitium to touch every last bit of collagen in the body.  Here these protons can share the information they contain.  This is how the tensegrity system gains information from sunlight.

Since sunlight forms an exclusion zone using H+, deuterium is excluded and its concentration in the blood rises.  Irradiated blood comes closer to the surface because of the electric and magnetic fields in light and these waves have many effects.  Releasing NO is one effect, but creating a pressure within the vessels also effects building a charge in all the blood products and cholesterol in the arteries.  The charge really build because all these things tend to be sulfated. (picture below)

As the zeta potential of the blood is raised by solar irradiation the blood heat up and this physocally effects deuterium more than H+.  Since RBC’s are highly charged on their surface a voltage is developed that discharges to the anions or anodes in blood.  This effect causes both hydrogen and deuterium to emit UV light.

Since most of the H+ is in EZ form of water it leaves the deuterium exposed in the blood to emit this light perferentially.  I have always believed this is why Pollack found that when the EZ forms in water its viscosity and is absorption spectrum changes.  It begins to absorb light at 270 nm.  This is deep in the short wave UV spectrum.  Not much sunlight gets to Earth in this range, yet water and hemoglobin absorb this light.  This looks unusual until you understand what makes UV light inside of us in this range.

When you compare H+ and deuterium emission it turns out deuterium is more capable of emitting a continuous and and more powerful light source of UV light.  Hydrogen-1 provides a very similar UV spectrum to deuterium.  In fact, both isotopes have been used in UV spectroscopes. However, scopes using deuterium have a longer life span and an emissivity (intensity) at the far end of their UV range which is three to five times that of an ordinary hydrogen.  This is why hemoglobin has strong peaks in the 250-300 nm range even thought this type of light is not often present in sunlight even in equatorial regions.  This was my clue that deuterium in the blood is why hemoglobin and the EZ used UV-C light from 250-280nm.  Deuterium is fully capable of creating a continuos spectrum in this range.  Remember blood plasma has 150 ppm of deuterium.  This tells you something deep about the quantum biologic systems.

 

 

The emission UV light from deuterium does not work like it does in excited electrons when they fall back to the ground state and give off a light photon.  That process in electrons is called atomic emission, where excited electrons emit radiation. Instead, deuterium uses an unusual molecular emission process, where radiative decay of excited states in molecular deuterium, causes the effect the UV light emission.

BLOOD AND CHLOROPHYLL ARE PORPHYRINS THAT DIFFER IN UV LIGHT

Blood does not glow under UV light, but it reacts with a chemical (luminol) that does fluoresce, so it can be detected after this reaction using ultraviolet light at a crime scene.  The interesting thing is that chlorophyll does fluoresce!

Chlorophyll makes plants green, but it fluoresces a blood red color under UV light.   This is how plants gain information for their protons in leaves. IF you want to check this out for yourself grind some spinach or swiss chard in a small amount of alcohol (e.g., vodka or Everclear) and pour it through a coffee filter to get chlorophyll extract (you keep the part that stays on the filter, not the liquid). You can see the red glow using a black light or even a strong fluorescent bulb, from your house, which (you guessed it) gives off some ultraviolet light.

Deuterium is the UV optical switch in blood that control melatonin levels in tissues to control mitophagy and apoptosis programs in mitochondria.  These two self regulating programs must be controlled for a good healthy life.  If control is lost in this mechanism from either the energy or information side of the equation disease is the result.   Mitophagy controls the quality and quantity of the water in the cytosol. This is why the cybrid studies I mentioned in TIme 4, 9, and 19 gave the results they did.  Cytosolic water must be free of deuterium.  Matrix and cytosolic water are where H+ is needed to impart information to light hydrogen as it is pulled from the anions in the TCA cycle and urea cycles.  Water links both of these cycle via fumerase at a place called Kreb’s bicycle.  This means water in the periphery of blood is a lot different composition inside mitochondria and this water creates a different size and shape of its crystalline form to changes cell water.  You blood plasma must have higher deuterium concentration by design.

Protonicity or proton conduction in water networks is how tissues gain the ability to know things via the information quanta passed to the orbital angular momentum of H+.  This is how energy and information are transferred from the sun to our atoms. We are made up of lots of atoms mostly considered bosons that collect light information. That is what life is a really at our core.

When the familiar red solar spectral line of the hydrogen spectrum is examined at very high resolution, it is found to be a closely-spaced doublet. This splitting is called fine structure and was one of the first experimental evidence for electron spin.  The small splitting of the spectral line is attributed to an interaction between the electron spin S and the orbital angular momentum L. It is called the spin-orbit interaction.

The familiar red H-alpha line of hydrogen is a single line according to the Bohr theory. The straight application of the Schrodinger equation to the hydrogen atom gives the same result. If you calculate the wavelength of this line using the energy expression from the Bohr theory, you get 656.11 nm for hydrogen, treating the nucleus as a fixed center. If you use the reduced mass, you get 656.47 nm for hydrogen and 656.29 nm for deuterium. The difference between the hydrogen and deuterium lines is about 0.2 nm and the splitting of each of them is about 0.016 nm, corresponding to an energy difference of about 0.000045 eV.

This corresponds to an internal magnetic field on the electron of about 0.4 Tesla.  Why is this detail important?  It is directly in the middle of the Earth magnetic field strength.  Remember that H+ and D both have unique magnetic moments because they have different quantum spin numbers.

The magnetic field magnitude at Earth’s surface ranges from 25 to 65 microteslas (0.25 to 0.65 gauss). Roughly speaking it is the field of a magnetic dipole currently tilted at an angle of about 11 degrees with respect to Earth’s rotational axis.  It is as if there were a bar magnet placed at that angle at the center of the Earth with respect to our protons.

Does anyone want to guess where magnetic strength is strongest on Earth?  The Yucatan peninsula. Does anyone want to guess why?  Does anyone want to guess why I recommend everyone sick go there now?  Illness is a lack of information redox in your cells.  You have been thinking this was all about energy flux because that is what the laws of thermodynamics suggested based upon a CLASSICAL interpretation of them.  Since 1960, that has fallen by the wayside.   You’ve now been introduced to really how the second law allows your cells to gain information how to stay far from equilibrium to do the things life does.  Nature will astound you when you see her magic.

You need to go the Earth’s library where more information can be transferred from the sun and Earth to your cells to fix any problem you have in the Yucatan.

Lesson over.  You’ve just been introduced to Quantum Thermodynamics of life.

 

This autoimmune disease is linked to a POOR connection the sun and Earth.  This is tied to your choices and lifestyle.  It may be an unpleasant message for some to hear but before you can get well you must know the things you control and can change to get a reversal.  Read this hyperlink if you think it is not true.

HYPERLINK

 

 

^^^^this is wise if you have MG.

 

 

^^^^do not be this type of primate if you have MG or want to avoid it in a 5G world.

OCULAR MYASTHENIA:

Over two-thirds of all patients with myasthenia gravis (MG) begin with symptoms relating to their vision. Overall, the ratio of affected females to males in generalized MG is 3:2 or higher. In ocular myasthenia, men are more frequently affected, especially after the age of 40. In addition, the average age of onset for generalized myasthenia is 33 years, while that of ocular MG is 38 years. The ocular motor system may be especially vulnerable to MG since it cannot adapt rapidly to variable weakness. The most common symptoms seen in patients with ocular MG are diplopia (double vision), ptosis (droopy eyelids), and incomplete eye closure. Compared to other involved skeletal muscles, only slight weakness of the extraocular muscle may cause diplopia and visual disturbances to occur. These symptoms occur due to the weakness of the muscle that controls eyeball and eyelid movement. Light sensitivity due to sluggish pupils may occur in some patients. Symptoms are frequently influenced by environmental, emotional, and physical factors. Some of these factors include bright sunlight, extreme temperature, emotional stress, illness, surgery, menstruation, and pregnancy, among others. Symptoms tend to be worse at the end of the day because of mitochondrial fatigue.

Symptoms

Diplopia or double vision results when the eyes cannot be focused as desired due to the weakness of one or more of the extraocular muscles which control eye movement. This most often occurs when looking up or to the side. To compensate for the weakness, the patient may tilt his/her head or turn their face to allow the stronger eye to work. For example, if the muscle which allows the eye to look upward is weak, the patient could tilt their head back to look up. Ptosis (to-sis) is the drooping of one or both eyelids, also due to muscle weakness. Fluttering or twitching of the eyelid may occasionally be seen. If both eyelids are droopy, one may be worse than the other.

Nystagmus or constant involuntary repeated movement of the eyeball in any direction may also occur in one or both eyes.

Diagnosis

The edrophonium (Tensilon) test is the first-line test for diagnosis of MG. The Tensilon test consists of injecting a small amount of medication edrophonium intravenously. If the patient has MG the ocular muscle weakness, the ptosis, and general muscle weakness and/or nystagmus will improve dramatically for a short period of time. In recent years an ice test is being more widely used. This is when ice is applied to the eyes, after a short period of time; the eyes will have an improvement of ocular symptoms. Usually, a blood test called acetylcholine receptor antibody titer (AChR Ab) is ordered as well. Additional blood work may include other antibody studies, thyroid profile, and a sedimentation rate.

Tests

A test to check for fatigue and weakness of the eye muscle which may be done by the examining doctor includes attempting to open the eyes while the patient tries to hold them shut, sometimes called a “peek sign”. This may result in one or both eyes opened, and the patient appears to “peek” at the examiner.

The “sleep test”, which is based on the tendency for MG symptoms to improve following rest, may be used in small children and patients who have allergies or sensitivity to anticholinesterase drugs such as Tensilon. The patient is placed in a quiet, darkened room and instructed to close their eyes for 30 minutes. The patient is photographed and eye movement is measured before and after the rest. The test is considered positive if there is an improvement in the ptosis and/or eye movement (motility) following the 30 minute rest period.

The morning/evening comparison test is similar in concept to the sleep test. The patient is photographed, and the ptosis and ocular motility are compared at different times during the day. Old photos are very helpful to determine how long the patient has had drooping of the upper eyelid.

The “Ice Test” is a simple test for ocular MG in patients who have ptosis. A surgical glove filled with ice is held against the droopy eyelid for several minutes. In ocular MG the patient can open his/her eye normally for a short period after the ice is removed. This shows the clinician this disease is related to inflammation/deuterium fraction (low pH of cell water), poor semiconductive currents in the electron tunneling along the inner mitochondrial membrane.

Electromagnetic radiation in the environment is capable of driving the disease.

”A significant change in pH of water (0.5-1.5 unit) was induced by a 30-irradiation at a frequency of 49, 50.3, 51.8, or 53 GHz, when the initial pH value was 6.0 or 8.0, but not 7.5. These results indicate the changes in the properties of water and its role in the effects of EMI of extremely high frequency. ”

The dielectric properties of water make it a sponge for electromagnetic radiation; particularly in microwave frequency range because of matching resonance. This link to nnEMF is rarely made in MG cases by clinicians. Anytime someone gets a new diagnosis I always ask them how much he or she use his or her cell phone for work and pleasure and if they hold it up to the side of their eyes. I also ask if they live close to an airport, TV or radio stations, or a Doppler radar installation. I also ask about military bases or HAARP installation in the area. It is well known that certain portions of the spectrum of light outside of the visible spectrum of light cause acidification of water. This is true in the atmosphere, oceans, and in our cells. We seem to be oblivious to these links.

“The absorption of electromagnetic radiation by water depends on the state of the water. The absorption in the gas phase occurs in three regions of the spectrum. Rotational transitions are responsible for absorption in the microwave and far-infrared, vibrational transitions in the mid-infrared and near-infrared. Vibrational bands have rotational fine structure. Electronic transitions occur in the ultraviolet regions. Liquid water has no rotational spectrum but does absorb deeply in the microwave region. Many mystery illnesses are due to the changing proton concentration in cells. We need to realize often this begins way before we meet the diagnostic criteria for most of these immune activated diseases. The reason it is missed is that allopathic and functional medicine are poor at understanding how the dielectric constant of water changes as the environment varies.

 

 

MORE SYMPTOMS

”Another simple test for ptosis is the “fatigue” test. This consists of having the patient look at an object held up by the examiner in front of the patient. After a short period of time, the eyelid(s) will droop in the person with ocular MG.

An MRI or CT scan of the head is often done to rule out other possible causes of the patient’s symptoms. Additional testing may also be needed to confirm the diagnosis. Myasthenia Gravis 101: The adenine nucleotide transporter 1 (Ant1) gene encodes an inner mitochondrial membrane protein that transports ADP into mitochondria and ATP from mitochondria to the cytosol. Mutations within Ant 1 have been shown to produce a syndrome of chronic progressive external ophthalmoplegia (CPEO) in humans. Myesthenia, however, appears more related to ANT 2 defects. extraocular muscles have much higher levels of ANT 2 mRNA compared to the limb muscles. ANT 2 is a nonskeletal muscle isoform previously described in the human heart. Its presence in the extraocular muscles may explain the lack of effects of ANT 1 loss, and it was the first documented difference between extraocular muscle and limb muscle mitochondria in the literature. Many textbooks blame MG on the release of acetylcholine into the synaptic cleft of skeletal muscles but they seem to forget that this process is electrically controlled by charged subatomic particles that control the release of calcium in mitochondrion that is the foundation of neurotransmitter release. Things like deuterium, fluoride, and bromine inside of cells doing things to mitochondria ruin the protein and light communication inside of cells because it disrupts the dielectric constant of cell water.  Things inside our mitochondria have to move fast and these things slow reactions down because there is not enough energy in the mitochondria of muscle afflicted by MG.  Below is an example how deuterium is tightly controlled by the location of substrates in the matrix.

Sunlight connects with mitochondria wirelessly via the blood.  People with MG need to understand you can develop symptoms of this disease with a lack of sunlight or a problem inside your mitochondria because the first steps in porphyrin synthesis occur inside mitochondria. Myasthenia gravis with thymoma has been associated with pure red blood cell aplasia.  This is a complete knockout, but I have a sense that porphyrin synthesis is very slowed in MG patients.  This is why many people with MG have other connective tissue disorders linked to and cannot tolerate some drugs.  It is also why many people are photosensitive to light and they stay out of the sun.  I believe this sense is linked to something in the skin that increases thermal sensitivity tied to dopamine creation in the muscle and skin.  That link is to defects in tyrosine kinase receptors in the skin that affects dopamine synthesis because of an excessive antibody load in the blood plasma.  The key defect in MG is the antibody production by B cells, and its collection in the blood, but these antibodies cause collateral damage few clinicians seem to be linking together even today.

The porphyrias are genetic disorders of heme metabolism, caused by a defect in an enzyme responsible for the synthesis of the heme molecule, which in turn is necessary for the production of hemoglobin, myoglobin, and cytochromes in the matrix. MG gravis can have a version of this disease but it is cause post translationally by things like deuterium/halogens in the mitochondrial matrix that ruin water flows and heme synthesis.  Heme is an oxygen carrier, and is essential for aerobic respiration and adenosine triphosphate (ATP) production via the electron transport chain. Cytochrome production is necessary for the metabolism of multiple drugs within the body, most notably through the cytochrome P450 system, and also mediates the removal of some toxic substances which is why some with MG cannot tolerate some drugs.   Muscles have heme requiring proteins in myoglobin, hemoglobin and the cytochromes in their mitochondria.  The heme biosynthetic pathway starts in the mitochondria, with the production of d-aminolevulinic acid from glycine and succinyl-CoA, which is catalyzed by the pyridoxine-dependent enzyme d-aminolevulinic acid synthase (ALAS). This is the rate-limiting step in heme production and is the site of feedback inhibition, with inhibition of ALAS by heme, the end product of this pathway.

So if these steps of heme synthesis are slowed or sticky inside of mitochondria FOR ANY reason, your red blood cells will not be able to turn over as fast, your P450 system used for detox, and your myoglobin in muscles can be affected.  Hemoglobin is a heme porphyrin and it is a light ferry that brings oxygen and light to mitochondria.  If RBC’s is defective because of poor heme synthesis they should and may not carry as much oxygen and light from your skin to the muscles with MG.  There is no one cause of this autoimmune condition.  Many physicians overlook the connection of MG to RBCs diseases.  When people do poorly in sunlight they should be tested for porphyrin issues because this links it to poor mitochondrial function in these MG patients.  I believe it is a lot more common than people realize because there is a STRONG link of MG to low vitamin D levels and poor oxygen delivery to muscles.  Vitamin D levels control how immune cells can function and this can affect the number of antibodies made to the Acetylcholine receptor and tyrosine kinase receptors in muscles.  Sunlight is normally a tyrosine kinase inhibitor.

 

 

This implies that MG can act as another severe allergy to nnEMF that impairs the release of acetylcholine in skeletal muscle. I fully expect MG and CPEO to increase DRAMATICALLY in incidence and prevalence in a 5G world which will use RF/microwaves to generate massive electric fields on the surfaces of things in the ionosphere and on the Earth’s surface. People live in this environment today and it will increase as technologic “progress” is fueled by the economy. Clinicians need to be ready for these expectations.

 

 

The ability of muscles to perform aerobic work depends on their mitochondrial volume density, with the assumption that the composition of these organelles is fairly constant across muscle types and mammalian species. One of these components is the electron transport chain, a series of multimeric complexes (complexes I–IV, plus the ATP synthase which is sometimes called complex V) in the inner mitochondrial membrane responsible for most of the aerobic ATP generation. Recently, it was found that the extraocular muscle mitochondria have lower content or lower activity of some enzyme complexes of the electron transport system, causing them to respire at slower rates. This means that the EOM have a lower basal metabolic rate than most other tissues in the body. This is puzzling given that the extraocular muscles are constantly active and aerobic capacity was predicted to be elevated, given their high mitochondrial content. This is an important teaching point. Longevity and health are tied to lower basal metabolic rates. Deuterium in the matrix or cytosol is capable of altering the metabolic rate of tissues.

These findings are not explained by differences in the ultrastructure of extraocular muscle mitochondria: the surface area of their inner membrane is comparable to values reported for other skeletal muscle. Furthermore, the differences are not generalized or systematic: complex II content and activity, and complex III content are similar in mitochondria from triceps surae (a limb skeletal muscle) and extraocular muscle. Complexes I and IV give a more puzzling result: their activities are lower, but their content is higher in the extraocular muscle mitochondria. These are multimeric protein complexes, and differential expression of isoforms of some subunits has been described in skeletal muscle and other tissues. Therefore, the content of some electron transport chain complexes (I, IV, and V) and the subunit composition of some others (I and IV) may not be the same in the extraocular muscles compared to limb muscles and may explain why these muscles are damaged preferentially in autoimmune diseases.

This demonstrates that the metabolic divergence between extraocular and limb muscles includes major differences in the composition and basic function of their respective mitochondrial populations. Intrinsic differences in mitochondrial structure and function may explain the susceptibility of the extraocular muscles to some hereditary and acquired mitochondrial myopathies such as MG and CPEO and related syndromes. For example, the extraocular muscles present the most severe age-dependent loss of mitochondrial respiratory complex activity among muscles. There is a significant increase in the number of fibers with cytochrome c oxidase defects in the extraocular muscles of humans and other primates, even when compared to other highly aerobic muscles such as the diaphragm and heart. This can be at least partially explained by mitochondrial DNA mutations, presumably due to reactive oxygen species generated during elevated mitochondrial respiration or present as part of a more generalized cellular oxidative stress.

Treatment

Reconnect with Nature!!!

Both ocular and generalized myasthenia gravis patients tend to have remissions and exacerbations at regular intervals, so that the medications that are used for treatment may need to be changed accordingly. Medications may include cholinesterase inhibitors such as Mestinon, steroids such as Prednisone, or other immunosuppressants used alone or in combination.In addition to medications, other options which may be used are plasmapheresis or IVIG therapy. These treatments offer only a temporary improvement and repeated treatments are necessary to sustain the effect. While thymectomy (removal of the thymus gland) is often recommended for patients with generalized MG, it is rarely used in purely ocular MG unless a thymoma is suspected.

In those people whose ocular myasthenia is not adequately controlled by medicine, several aids are available. In many patients, simply wearing a patch over one eye will eliminate the double vision. The patient may alternate the eye patch from one eye to the other to avoid eye strain. Another method is wearing one contact lens which is opaque (can’t be seen through). This may also be changed periodically from one eye to the other. Ask the ophthalmologist how often this should be done. Special prism glasses may also help to correct double vision in some cases.

When both eyelids droop, taping one eyelid open may improve vision. The use of non-allergenic tape such as paper tape is suggested. Once again, alternating eyelids is recommended to prevent eye strain. Another way to hold one or both eyelids open is to have ptosis bars or eyelid crutches attached to the eyeglasses. These are thin, flexible wires which attach at the bridge of the nose and are free-floating at the other end or attached to the frame near the hinges. The wires rest against the eye socket and hold the eyelid open like a brace or crutch. These devices must be carefully fitted and adjusted by an ophthalmologist. Most patients report that the eyes adjust to the bars after a period of time. And they are much more convenient than taping the lids open. Since the eyes can’t blink normally, dryness and irritation may result. It is important to remove the glasses frequently to allow the eyes to close so that they can be moistened. Some MG patients have advised that every ten minutes or so is a good guideline. Artificial tear drops and forced blinking may also help. If the patient has double vision in addition to drooping eyelids, one eye should be allowed to close and the other be held up by the ptosis bar.

Remember this wisdom does not grow in every clinicians garden.  You need to think differently about this disease if you have it and want to avoid it.  Mitochondriacs do not settle for half truths on any disease.

 

 

CITES:

http://www.ncbi.nlm.nih.gov/pubmed/17969925

https://en.wikipedia.org/wiki/Electromagnetic_absorption_by_water

https://www.researchgate.net/post/Relationship_between_pH_and_conductivity2

http://pmj.bmj.com/content/80/950/690

 

Just listen to the video above…….If you don’t understand how important this video is to share just leave this page as soon as you can.

We just had several unusual behaviors occur in cities already testing 5G networks. We had the Santa Rosa fires, the Austin bomber, and a rookie NFL reciever have a psychotic break in Los Angeles. Many people will not see the connection because they do not understand the science behind it. I lay out this science every day on my Dr. Jack Kruse facebook page, my Patreon blog, and on my website forum.

That is not what this post is about. This post if about teaching and sharing wisdom about technology networks that are going to be unleashed on large portions of our country. I expect a massive change in the health of many people in places where 5G is first operational.

 

 

We are close to the 5G tipping point.

What is a tipping point?

The Tipping Point explains how ideas spread like epidemics and which few elements need to come together to help an idea reach the point of critical mass, where its viral effect becomes unstoppable.

 

 

Mitochondriacs need to begin to step up to the plate and stop talking a good game and do something about it now.

Three kinds of people are responsible for getting ideas to tip:

Malcolm Gladwell specifically points out in his book, Tipping Point,  three kinds of people that turn ideas into epidemics:

1. Connectors – they have a massive social network, with many acquaintances and allow ideas to spread from one social group to the next.
2. Salesmen  – the boast about ideas they love and their incredibly positive energy is contagious.
3. Mavens  – they hoard information, in order to be a source of great tips to their network, the people of which they greatly influence with their advice.

If you want your idea to go viral, getting it in the hands of a few of these key players is crucial to hit critical mass.  I am hoping this video is shared with everyone who you EVEN think might be a person like this.  If you want to help becoming a facilitator of tipping this 5G message is huge.  I am asking you to do something you might not have ever done.  Why I am asking you to do this?  Because all of us are at risk and if your neighbors do not understand how radiation works their use and over use wll get you and your family sick.

If you thought secondary smoke was risky you have no idea how bad electromagnetic pollution is for your mitochondria and health.

 

 

Genius always strives to answer questions the ordinary forgot to pose. Each one of you have genius in you put there by nature. It is time for you to stop ignoring it and engage.

Focus on your genius. Genius is the recovery of the connection to nature at will. The mediocrity of modern man knows nothing higher than itself because it drunk on the money tied to technolgy; but talent of nature instantly recognizes genius. Curiosity fuels action which builds wisdom through the collateral damage of discovery.

I’m now begging for your help. I cannot do this alone.

Delegate as much as you can that is not your core genius to someone else who can help, and take concrete steps toward the attainment of your goals.

I am doing my part right here right now.

It’s not for the lack of study, or data, or evidence, but simply a lack of discernment about who we trust, before embracing new evolutions in technology. The head of FB just sold 50 million of its users information to weaponize propaganda.

 

 

Space X, Facebook, Twitter, Apple, Google, Linkedin, Yelp—the whole field is built on the idea that an individual’s data is a commodity to be mined, without regulation, like bauxite or titanium for profit of the 1%.

Do not think school boards and churchs are not in the business of doing the exact same thing to you and your kids without your consent. Here is a picture of a church steeple in an American city. Your kids are being irradiated everyday in school and teachers now are getting rid of books for latops and ipads because of the wishes of the 1% who run these companies. The Internet of things needs 5G to operate and it is the most serious viral infection man has ever faced. It is affecting 7 billion people on Earth. No virus has had that infective power to harm people.

 

 

Silicon Valley clings to the conviction that “free speech” means that host corporations have no responsibility for the consequential falsehoods, threats, or exploitative images published on their profit-making platforms; that the vast wealth generated by these ventures can be concentrated in the hands of a tiny technocratic elite; and that these companies and their satellites are justified in incorporating in tax havens to protect themselves from even the minimal civic responsibilities incumbent on ordinary businesses. The liberal facade of the tech industry on social issues masks broader rapacious betrayals of the broader social contract with the public.

This situation with 5G is the perfect application of the “boiling frogs” analogy. We are drowning in our ignorance, and gullibility and we are allowing it to happen to us. If people refuse to question, what authorities, government, trusted institutions, and especially the media are selling us, we will surely meet our end. Not as helpless victims who never had a chance or a choice, but as willing participants, who would rather obediently, and orderly march to our doom, than confront the reality of the lies we are sold daily, as truth and fact.

The natural quantum synergies between light frequencies and chemicals, including heavy metals, and radiation, including that emitted by electricity, WiFi, cell towers, cordless phones, cell phones, wireless everything in total will lead to collateral damages few will predict in a 5G world.

ACTION PLAN:

Adaptation is not hard at all for those who learn to properly think.  Infact, I am going to tell you the single most important part of “Optimal Health for a mitochondriac” before you change a thing about your diet or exercise program, you must learn to cultivate your mind.  The world is a comedy to those that think really well because they can spot bullshit dogma a mile away; it becomes a tragedy to those that feel they know the answers without really doing the due diligence.

You have to wake up the sleeping people around you what is really going on in California’s technology abyss.

I hope you all realize that one of the things that have me concerned about the AC power grid in combination with the power density is jump conduction.   This means waves forms with unusual topology and frequencies can jump from the 5G network directly on to conductors like the power grid.  Now we have hardcore data that we can find the fingerprints of the 50-60Hz global power grid in the entire ionosphere.  I can only imagine what we will find in our ionosphere in a 5G world.  Just flying in a plane might be a death sentence.   Instead of “Death by a 1000 Papercuts,” the nnEMF issue could be described a bit more like “Death by 1000 Points of Light humans built but have never faced before in evolutionary history” There will be many conversations soon where a person will making an argument that one phone’s RF/microwave beam isn’t going to be a problem for health or the environment. 5G is going to be a lot worse than second-hand smoke risks.  So we can now open up Pandora’s Box to make it clear that the entire planet now pulses with 50 and 60 hertz frequencies due to our power grid, and this wasn’t happening at all just 150 years ago. You can be sure the skeptic response was “so what.” Our responses will be, “yeah, those Van Allen belts don’t have any influence on life, do they?”

They do and here is the proof:    LINK

I am asking for your help now.

If you put a limit on what you will do, you put a limit on what you can do.

Most people really don’t want the truth, they just want constant reassurance that what they believe is the truth.  My mouth is not a bakery.  I don’t sugarcoat anything.  If you ask me my opinion I’m going to tell you the truth, no matter what you want to hear.  That is how you help people who remain unaware of what they don’t know is the most important part of the recipe.

That tipping point is here.  Technology using 5G hurts our entire species in ways most of you may not understand.  Understanding now is not important.  We just need you to share the Congressman video above to get the message out we’ve been lied to by the government that technology has no downsides.

Today, we got confirmation that the government NTP toxcity study on 2G and 3G networks that showed tumors in mice was confirmed on a larger scale tonight.

WHAT WAS NTP TOXICITY TRIAL AND WHAT DID IT SHOW IN MAY 2015

Federal scientists released partial findings in May 2015 from a $25-million animal study that tested the possibility of links between cancer and chronic exposure to the type of radiation emitted from cell phones and wireless devices. The findings, which chronicle an unprecedented number of rodents subjected to a lifetime of electromagnetic radiation starting in utero, present some of the strongest evidence to date that such exposure is associated with the formation of rare cancers in at least two cell types in the brains and hearts of rats. The results, which were posted on a prepublication Web site run by Cold Spring Harbor Laboratory, are poised to reignite controversy about how such everyday exposure might affect human health.

Researchers at the National Toxicology Program (NTP), a federal interagency group under the National Institutes of Health, led the study. They chronically exposed rodents to carefully calibrated radio-frequency (RF) radiation levels designed to roughly emulate what humans with heavy cell phone use or exposure could theoretically experience in their daily lives. The animals were placed in specially built chambers that dosed their whole bodies with varying amounts and types of this radiation for approximately nine hours per day throughout their two-year life spans. “This is by far—far and away—the most carefully done cell phone bioassay, a biological assessment. This is a classic study that is done for trying to understand cancers in humans,” says Christopher Portier, a retired head of the NTP who helped launch the study and still sometimes works for the federal government as a consultant scientist. “There will have to be a lot of work after this to assess if it causes problems in humans, but the fact that you can do it in rats will be a big issue. This study has been the first that has actually concerned experts and it should scare the hell out of the non-expert.  This is the largest biologic experiment ever put on the human race. More than 90 percent of American adults use cell phones. Relatively little is known about their safety, however, because current exposure guidelines are based largely on knowledge about acute injury from thermal effects, not long-term, low-level exposure as the congreeman mentions in the above video. The International Agency for Research on Cancer in 2011 classified RF radiation as a possible human carcinogen. But data from human studies has been “inconsistent,”  The only reason it is considered inconsistent s because the wireless carriers have hired scientists to create studies that create doubt to the true effects of electromagnetic fields.  If you read my page you already know how powerful these fields are on cells. The researchers found damning findings in this study that as the thousands of rats in the new study were exposed to greater intensities of RF radiation, more of them developed rare forms of brain and heart cancer that could not be easily explained away, exhibiting a direct dose-response relationship. Overall, the incidence of these rare tumors was still relatively low, which would be expected with rare tumors in general, but the incidence grew with greater levels of exposure to the radiation. Some of the rats had glioma—a tumor of the glial cells in the brain—or schwannoma of the heart. Furthering concern about the findings: In prior epidemiological studies of humans and cell phone exposure, both types of tumors have also cropped up as associations.

The part that should send chills down all your backs?  In contrast, NONE of the control rats—those not exposed to the radiation—developed such tumors. For me the smoking gun was that findings were mixed across sexes: I would expect this because of the difference of myelination patterns in nocturnal mice and how their retinae are built to sense radiation.  More such lesions were found in male rats than in female rats.  This implies in diurnal mammals like humans more females would be expected.  This is a clue why females have higher autoimmune conditions in our modern world.  I expect the association to only grow stronger from here.  Cell phones are exponentially worse than cigarettes and I expect the settlement to dwarf big tobacco.  If you continue to ignore the melody of the research of nnEMF you too will be touched by one of these diseases.   HYPERLINK TO NTP

Now we have a big study confirming the NTP toxicity report results released tonight.  This a big deal here folks.  HYPERLINK

Before the truth can set you free, you need to identify which lie is holding you hostage. 

 

 

How can a physician help patients far outside their clinic?   Don’t hate the health/medical media; become the health media by speaking truths of nature online about public health issues that affect us all.  Distribute natural laws yourself to the masses who are starving the truth. Today, readership is highly dependent upon format and distribution as much as it is on content.  Where are you? Where do you ‘need’ to be? Distribution of health information is the direction where things are going in medicine.  The paradigm mocks this distribution as pseudoscientific. That ignorance is a huge advantage to people like me.  PEER review journals are old media in medicine.  Their rules are no longer my rules.  If you want to change the world you take that change directly to the masses with illness and sickness who are getting Rx’s over truth.  You, just reading and sharing this blog, could make a difference to others.  Distribution takes things from where they are now, to where they are needed for others.   Talents, gifts, and abilities are distributed to us. We are supplied with them and it is our responsibility to stir up those gifts, to fan the flames of those gifts.  So where are you now?

Please help by sharing this blog to everyone you can think of.

Thank you in advance,

Jack Kruse

 

Solar storms bring space weather to the surface of the Earth.  The space environment cause humans a lot of problems.  For those who do not believe this just take a look at a human who spent a year in space and has an identical twin.  It is proof what nnEMF from the sun can do to us.  Scott and Mark Kelly are identical twin brothers — at least, they were until Scott spent a year living in space.

When Scott Kelly returned to Earth after a 340-day voyage aboard the International Space Station (ISS) two years ago, he was 2 inches taller than he’d been when he left. His body mass had decreased, his gut bacteria were completely different, and — according to preliminary findings from NASA researchers — his genetic code had changed significantly because his methylation pattern changed. Interestingly, Scott Kelly has since shrunk back down to his initial prespaceflight height. but it took close to 6 months to occur.

SO WHAT HAPPENS WHEN SOLAR SPACE WEATHER COMES TO EARTH?

Could this effect mimic what humans might face in a 5G world?  We’ll get a chance to see that this weekend.

Researchers indicate that changes in Space Weather may have a negative impact on human health and physiological state through the influence of Geomagnetic Disturbances on the human brain’s functional state. The video above also gives you several more cites that show this effect is real.

A G1 (Kp=5) storm watch is in effect for March 14 & 15th in 2018! The aurora possibly visible at high latitudes due to the arrival of a co-rotating interactive region (fast solar wind catching up with slow) and a coronal hole producing fast solar wind.  People at these higher latitudes might see geomagnetic effects in humans.

 

 

Studies conducted in different places on the globe (Russia, Germany, Hungary, Japan, Poland, Azerbaijan, Israel, Lithuania, etc.) show the correlations between high Solar and Geomagnetic Activity and increased Traffic Accidents.

In terms of effects, I found the following factors definitely influenced by Earth’s geomagnetic activity (GMA). There are probably many more effects yet to be documented in the coming 5G world:

Higher hospital cardiovascular and cerebrovascular accident mortality

A higher number of deaths of outpatients from acute myocardial infarction (heart attack)

Higher diastolic blood pressure in healthy blood donors and hypertensive patients

A higher number of blood platelets, prothrombin index, and platelet aggregation (risk of coronary thrombosis)

Greater human blood plasma viscosity (also risk of clotting with flights and inside the power grid)

More bone loss in younger patients without any risk factors.

Hormone panel collapse due to pregnenolone syndrome.

Massive infertility in both sexes

Sleep disorders will skyrocket

I fully expect altered levels of human prolactin and 17-ketosteroid levels with the geomagnetic stressors from alien magnetic fields in a 5G world.  In some people the levels will be raised and in others they will be crashed.  The environments varying magnetic flux will be a huge clue to clinicians who are wise that the cause is a varying magnetic field in the patients house/job/school.

The urinary 17–ketosteroids have been shown to be derivatives of testicular and adrenal cortical precursors in humans.   The measurement of urinary 17–ketosteroids should serve as a rough index of the secretory activity of the testis and adrenal cortex and as an aid in the diagnosis of certain endocrinopathies caused by altered magnetic field from 5G.  Usually the amount of 17-ketosteroids were increased (0G-3G world) in diseases in which there is hyperfunction of the adrenal cortex due to tumor or hyperplasia, and decreased in lesions that impair the function of the adrenal cortex. Other conditions where we saw the alteration of the excretion of these hormone prior to 2005 were myxedema, eunuchism, gout, and arthritis.  In a 4G and 5G world we have begun to lose this linkage when you look for it clinically.  This explains why physicians are beginning to see lab values that make no sense to some.  The conditions of existence in cities is no longer stable because of electromagnetic pollution.

In females we have already seen many unusual reports of early puberty associated with early periods and persistent early infertility. During adrenarche the adrenal cortex secretes increased levels of androgens such as DHEA and DHEAS, but without simultaneous increased cortisol levels.  Cortisol levels are linked to ACTH levels.  ACTH levels are linked to pro-opiomelanocortin (POMC) levels made in the retina and brain.

Early bleeding and infertility has made fertility doctors quite rich and I expect women to become worse and not better in a 5G world.  The reason why is tied to how 17-ketosteroids are controlled by magnetic flux.  As women matures, her tissues expand their ability to make more ATP as she grows, and the spinning Fo head of the ATPase increases its spin rate and this in turn, increases her endogenous magnetic fields.  This occurs as she sheds deuterium, and her matrix begins to favor DDW in her matrix as she matures.  This magnetic change has been noted in MEG data in women going through puberty.

Adrenal 17-ketosteroid secretion gradually begins during midchildhood as a result of adrenarche. Adrenarche is characterized by a change in the pattern of the adrenal secretory response to ACTH.  ACTH is released from POMC.   POMC is a precursor polypeptide with 241 amino acid residues.   POMC is cleaved to give rise to multiple peptide hormones in humans. Each of these peptides is packaged in large dense-core vesicles that are released from the cells by exocytosis in response to appropriate stimulation:

• α-MSH produced by neurons in the arcuate nucleus has important roles in the regulation of appetite.  POMC neuron stimulation results in satiety.   The leptin melanocortin pathway I wrote about in the Cold Thermogenesis 6 blog is linked to alpha MSH/POMC.  Alpha MSH is also tied to sexual behavior, while α-MSH secreted from the intermediate lobe of the pituitary regulates the production of melanin in human skin.  This makes links the skin to the brain.
• ACTH is a peptide hormone that regulates the secretion of glucocorticoids from the adrenal cortex.  This ties it to flat lined cortisol curves in adrenal stress testing.
• β-Endorphin and Met-enkephalin are endogenous opioid peptides with widespread actions in the brain related to mood and behavior.  Nature has built humans to be addicted to nature.  5G counteracts these effects.
• Prior to adrenarche, ACTH elicits only cortisol secretion; with the commencement of adrenarche, ACTH elicits both cortisol and 17-ketosteroid secretion.
• There are marked increases in 17-hydroxypregnenolone and DHEA production that lead to DHEA-sulfate (DHEAS, the sulfated derivative of DHEA) becoming the predominant androgen secreted by the adrenal gland.

These adrenarchal changes are associated with the development of the zona reticularis of the adrenal cortex, the adrenal zone that produces large amounts of DHEA and DHEAS

Dopamine is made by AM sunlight and it inhibits the release of prolactin. Prolactin normally increases in dark. Prolactin secretion seems to regulate the pro-opiomelanocortin gene’s expression.  This expression seems to make the retina very sensitive to AM sunlight.  Night time is when cells “feel” the higher magnetic flux of the Earth.  During daytime magnetic flux decreases and electric fields predominate.  Our hormone cycles are linked to these diurnal variations.  The surge of prolactin is normally quite large in normal darkness but is significantly diminished in artificially lit environments after sunset because of melanopsin. This has big implications for modern humans who have built a world filled with fake light at night.

The reason is that prolactin release is coordinated with sleep cycles where autophagy is at its highest efficiency and where Growth Hormone is released between 12AM-3AM.  If this is diminished for any reason, we generally see lower DHEA levels clinically and higher IL-6 levels on cytokine arrays. Remember when we see lowered DHEA levels this sends a signal to our gut flora that something is amiss and this allows LPS to get across the brush border. It allows more permeability of our intestinal brush border to inflammation that destroys signaling in the liver and brain.

HOW DOES THE BRAIN REACT TO MAGNETIC ENERGY FROM EMF?

“Magnetite is an excellent absorber of ultraviolet radiation and is also good at transmitting visible light. This may mean that magnetite uses these light frequencies in cellular signaling as well.”  QED works in ways most cannot fathom.  HYPERLINK

 

 

This picture and link above says a lot.  Magnetite can change hydrogen bonding networks in the CSF and this information can be shared with the blood because CSF reenters at the blood at the arachnoid granulations adjacent to the venous sinus in the dura and skull.

HORMONES ARE AFFECTED BY THIS MAGNETIC ENERGY

17-ketosteroids are a group of compounds derived from complex steroids produced by the adrenal cortex, testis, or ovary. Usually, the amount is increased in diseases in which there is hyperfunction of the adrenal cortex due to tumor or hyperplasia and decreased in lesions that impair the function of the adrenal cortex.

Other conditions such as panhypopituitarism, myxedema, eunuchism, gout, and arthritis may alter the excretion of the 17-ketosteroids.

Higher levels of human growth hormone.

More severe migraine headaches

Significantly more frequent heart rhythm disturbances – supraventricular and ventricular extrasystoles as detected with the electrocardiogram (ECG)

A higher number of sudden cardiovascular deaths (follows from previous factors)

A greater involvement of the inferior wall of the heart than the anterior wall in acute myocardial infarction

The anterior/inferior wall ratio increases with the level of the GMA.

This is quite a list. I have also remarked on the noted increase in car accidents and in hospitalizations due to psychiatric disturbances.

So there is no question these solar storms do affect us, probably more than we realize.  It appears when alien non native magnetic fields are around our bodies we react badly to this.  In a 5G world these antenna system arrays will give these signatures so you should learn how to use a gaussmeter to search for these alien fields when they go live in your environment.

When people begin to act in bizarre fashion around you consistently, if you are wise, do chalk it up to coincidence.  Remember this blog.  The sun’s magnetic field can cause human behavioral change and I fully expect manmade magnetic fields will do the same.

SUMMARY

If you don’t believe me explain why Google has this patent?

Monopoles can separate neutrino flavors in sunlight FYI.  My members already heard my ideas tied to this in my April 2016 webinar.  You Patrons might want to listen to that bad boy.  It is EPIC.  I believe neutrinos are the key to unleashing the energy in a proton (H+) in the matrix.  And Google knows that 5G is going to induce magnetic disease so making an artificial monopole will offset their tech risks.  This patent proves my intuition is pretty solid.

 

 

In a 5G world with jump conduction, the power grid, gas pipes, and water lines will conduct abnormal magnetic flux to affect our biology.  We may turn out just like Scott Kelly.  I do not expect anyone labs to make sense in a 5G world.  You need to be aware that doing labs might really confuse your experts and they likely will have no idea why.  Now you do.

CITES:

http://www.academicjournals.org/article/article1380707205_Verma.pdf

http://ru.iszf.irk.ru/images/7/76/340-343.pdf

http://science.nasa.gov/headlines/y2009/21jan_severespaceweather.htm?list40968

https://www.livescience.com/62000-scott-kelly-dna-twin-study.html

 

EDIT:  This post was deleted by all social media platforms I posted it on in Early March 2018.  So I decided it was so important that I wanted my members and patrons to read it fully.

MITOCHONDRIAC CREDO 21:  YOU MUST HAVE COURAGE TO FIGHT POWER WITH WISDOM BY USING YOUR COURAGE AS CAPITAL

Yep, gov’t won’t come to save us… here is an Ultra-powerful blog by Dr. Andrew Marino that should resonate with every mitochondriac I teach!

“Thirty years ago I published this editorial (Where is the EPA’s sense of decency?, Journal of Bioelectricity 3(12):1–2, 1984).

The Environmental Protection Agency (EPA) was founded in 1970 “to protect and enhance our environment today and for future generations.” During the next decade, it earned a reputation as one of the more respected federal agencies. Its decisions were generally well-reasoned and occupied the middle ground. In 1980 Ronald Reagan appointed Ann Gorsuch as Administrator of the EPA, a choice widely criticized at the time as being based on political grounds. During the next several years there was an exodus of key professionals, and the EPA became a demoralized, do-nothing Agency. Following the Superfund scandal, William Ruckleshaus was appointed to head the EPA. He was supposed to replace politics with science as the basis for EPA decisions and set the Agency moving again. Under his leadership, however, things did not improve significantly.

 

 

After examining the way the EPA responded to evidence of formaldehyde’s carcinogenicity, an MIT professor reported in Science (222, 894, 1983) that the Agency’s actions revealed “the interplay between politics and science policy in regulatory determinations. In some cases, there were significant and unjustified departures from reasoned decision-making.” The Agency’s decision was, basically, to do nothing. An EPA official delivered essentially the same message to a national conference on toxics in ground-water: “We don’t have any quick fixes. This is going to be a long-term problem.” Much the same thing occurred in the area of lead poisoning. A 1979 study published in the New England Journal of Medicine showed that children with high lead levels scored lower on IQ tests. The EPA then assembled what official of the National Institute for Occupational Safety and Health called a “hanging jury” (Science, 222, 907, 1983) which strongly attacked the study, thereby destroying the main argument for holding lead pollution to low levels—that is, the main argument for EPA to take action.

 

The situation reached a new low with the efforts of the EPA in the matter of safety limits for environmental exposure to electromagnetic fields. In its Draft Study, the Agency’s staff arbitrarily adopted the approach that only thermal effects need be considered. But since there are no significant thermal-level exposures in the environment, the conclusion pregnant in the Draft was that there is no need for action to protect the public health. Ruckleshaus himself appointed a panel to review the Draft which consisted almost exclusively of individuals well known for their thermal-effects-only viewpoint. The majority view among scientists world-wide—that there exist biological effects due to non-thermal electromagnetic fields—was virtually unrepresented. It was not surprising when this newest “hanging jury” largely endorsed the staff’s approach. Worse still, was the avowed purpose of the EPA which is to issue so-called guidance to the twenty or so Federal Agencies that have a role in regulating the electromagnetic spectrum, and not to enact regulations pursuant to its broad congressional mandate. The EPA intends to palm off its responsibility to other federal agencies that have vastly less expertise and that are even more certain not to act.

 

 

The EPA was created by Congress to protect Americans from risks and threats against which the individual is almost completely defenseless. The public expects the EPA to be honest and fair, and to make decisions that protect the health of the American people. Instead, the EPA’s recent performance has been woefully reminiscent of what occurred at the McCarthy hearings 30 years ago when attorney Joe Welch, in complete revulsion of the Senator’s performance, said ‘You have done enough. Have you no sense of decency, sir? At long last have you left no sense of decency?’

 

During the halcyon days of the early 1970s, I was a young scientist, a young lawyer, and still under the influence of the philosophical outlook I had learned from the Jesuits, especially the idea of pursuing the common good. When I wrote the editorial, I interpreted the descent of the EPA into mediocrity as a transient aberration wrought by political leaders who had chosen to remain perpetually ignorant of science because that perspective served and fueled their notion of personal freedom that was so outlandish as to be antithetical to the common good. But in the twilight of my still-active career in science, I have a deeper understanding regarding the distinction between the natural trajectories of federal agencies whose primary mission is to protect the public, like the EPA and the FDA, in distinction to federal agencies whose primary mission is to set the rules whereby human beings can function as warring atoms of self-interest, like the FCC and the SEC. I see now that the fate of all protective federal agencies is to sink into mediocrity because they are inherently at war with powerful interests that promote extreme personal liberty. These agencies avoid operating on a war footing, which is dangerous and unstable, by always seeking a middle ground between common sense and rational science on one hand, and the fervent desires of radical pro-personal-freedom constituencies, whether motivated by money, philosophy, or religion. Thus mediocrity was in the EPA’s genes, and it should not be criticized as harshly as I did in the editorial.

My error back then—and I was not the only one who committed it—was to assume that federal agencies operated primarily on behalf of the public good. They do not. They are primarily arbiters of the eternal war between the Jesuit concept of the public good and the Ayn Rand concept of the private good. What I had perceived in 1980 as a Reagan-led transient period in the EPA’s evolution was actually the end of the transient period between the high hopes we had in 1970, and the attractor of mediocrity that appeared in 1980.

Independent thinking and reasoning was another equally important principle I learned from the Jesuits. If you adopt that perspective and make an effort to acquire information about the world rather than simply dwelling on the content of your own mind or the vividness of your own beliefs, you will arrive at the notion of personal responsibility. Everyone gets sick and dies. The only salient questions are how long before those processes develop, and what the quality of life will be when they do. If your primary goal is to optimize life and health, the information needed to do so is available, not like an apple to be reflexively picked and eaten, but like something to be discovered after a proper effort. 

You have the responsibility to seek that information. It would be foolish to expect the government to keep you healthy and lengthen your life. If you choose not to make the effort, then you can still hope that there will be a pill or an operation that will fix your problem.”   —–Dr. Marino

 

 

You are only as good as your daily routine.  That routine must contain a date with the sunrise every AM.

VIDEO

 

 

SUMMARY:

It’s really sad people can’t find their way out of the maze!  But they cannot by how the system designed its methodology to study the etiology of our problems today.  The light from technology was a major blow to cells and now 5G might be “the kill shot” for many with a poor redox.  Money cannot and does not buy human happiness. We may wish the ‘corporatocracy’ understood that because they keep throwing us and our health under the bus for profit.  It will not end until you put an end to the cycle.

Yes, the natural way is a good life. No doctor is a Moses, instead, they should act like Noah for their patients.  This should cause a collective ‘Gulp’ from mankind, but is it???? We keep buying technology upgrades all the time.  Do you follow crowds?  What if the crowd is going in the wrong direction off a cliff?  That’s profound insight in a 5G world.

 

 

With respect to the government and nnEMF/5G/blue lit screens: Talk from the government scientists at the NIH is cheap and people who talk and don’t do are easily detectable by the public because they are too good at talking bullshit.  What is Skin in the Game? The phrase is often mistaken for one-sided incentives: the promise of a bonus will make someone work harder for you than you can do for yourself.  If you are not good enough for yourself, you are good for no one.   For the central attribute is symmetry: the balancing of incentives and disincentives, people should also be penalized if something for which they are responsible goes wrong and hurts others: he or she who wants a share of the benefits needs to also share some of the risks.

The mitochondriac argument for “skin in the game”  is that there is an essential aspect: filtering and the facilitation of evolution. Skin in the game –is really a filter –is the central pillar for a new sightline the organic functioning of systems, whether humans or natural. Unless consequential decisions are taken by people who pay for the consequences, the world would be vulnerable to total systemic collapse.  You must have skin in your own game folks…………..no one is coming to save you.    The NIH funds all research via the government.  They want no one studying the effects of the spectrum of light for communications because it is the cornerstone of the US economy now.  Our biggest corporations in technology, along with the “people’s government” has elevated a few experts they have selected for a specific purpose.  These  “educated” but cosmetic experts have no skin in the game and will never learn from their mistakes, whether individually or, more dangerously, collectively.  And they were chosen by the paradigm precisely for this reason.  

Their job is to lead you to a cliff.  

Your job is to see it before it’s too late.  

Will you?  

VIDEO FOR MORE DEPTH IN UNDERSTANDING 

CITES

Conversations with Barry Murray and Mayuri. 2014-2018.

https://www.patreon.com/connectedathlete/posts

http://andrewamarino.com/blog/

Nassim Nicholas Taleb.  Fooled by Randomness: The Hidden Role of Chance in Life and in the Markets. 2008

Nassim Nicholas Taleb.  Incerto includes The Black Swan (2007–2010), The Bed of Procrustes (2010–2016), Antifragile (2012), and Skin in the Game (2018).

http://healthcastnow.libsyn.com/size/5/?search=jack%20kruse

https://www.evanbrand.com/blog/269-dr-jack-kruse-on-5g-emf-and-moving-south

Many trauma patients require implantable hardware for treatment of their spinal and bone injuries. One of the concerns patients frequently raise is whether this may cause a problem at TSA airport screening checkpoints (Transportation Safety Administration).

The answer in the past was probably “yes” because screening used more metal detection and less RF scanners.  If you travel into a country like Mexico regularly as I do, metal detection is still the defacto screen because it is cheaper than the new RF scanners used in the USA and EU.   Papers have shown in a 2G-3G dominated world in the mid 2000’s  that approximately half of implants can trigger the metal detectors.  Once triggered the patient is slowed down and subject to a pat down search.  I’ve even had patients tell me that the TSA agents have asked about their scars. Many patients ask me for letters about their surgery but I inform them that letters from me won’t help.  I have a few TSA agents as patients and they told me do not bother writting these letters.  They are trained not to pay any attention to them.   It turns out that overall, 38% are detected when the scanner is set to low sensitivity and 52% at high sensitivity.  I have found certain airports vary their settings often based upon flight origination and the type of people on the flight register.

 

 

Here is a more detailed breakdown:

• Lower extremity hardware is detected 10 times more often than upper extremity or spine implants
• Older spinal implants are more easily found because of their bulk but not the type of metal used by the implant makers.  If it is a multi-level fusion detection is more likely.
• 90% of total knee and total hip replacements are detected
• Upper extremity implants such as shoulder, wrist and radial head replacements are rarely detected
• Plates, screws, IM nails, and wires usually escape detection because they are smaller.
• Cobalt-chromium and titanium implants trigger alarms more often than stainless steel.  This one surprised me because older implants are often made of stainless steel.  The newer implants use the transition metals and this usage is likely going to cause patients a bigger problem in a 5G world because of how RF/microwaves interact with the D shell electrons of these metals.

I am a bit concerned about this topic because it is one aspect of medicine that most physicians will not link to the new 5G networks and their patients content of metal.  Why do I say this?

Recently, the FDA is requiring a new class warning and other safety measures for all gadolinium-based contrast agents (GBCAs) for magnetic resonance imaging (MRI) concerning gadolinium remaining in patients’ bodies, including the brain, for months to years after receiving these drugs. This warning also makes me very concerned about retain metal nanoparticles in the skin via tattoo’s.  The image below shows the metal partcoles reacting the the RF pulses and magnetic field of the 1.0 Tesla magnet in one of my patients.  You can see the shielding effect on the L4-5 and L5-S1 disc adjacent to the metal particles embedded in her skin as a result.  The surface topology effect of metal in a 5G world is going to be serious risk.

HYPERLINK #1

HYPERLINK #2

Most metal implants are left in our patients post operatively so they act as a reservoir of metal.  In the most recent FDA release on Gadolinium retention, the gadolinium has not been directly linked to adverse health effects in patients with normal kidney function, and FDA has concluded that the benefit of all approved GBCA’s continues to outweigh any potential risks.  This warning was made in a 3G/4G world.  I am concerned that the same will not be true in a 5G world.

 

 

If any patient knows that their implant triggers the detectors, they have two options:  request a patdown search (smartest move), or volunteer to go through the full body millimeter wave scanner with its own risks for the surfaces. This device uses RF radiation to look at everything from the skin outwards, and will not “see” the implant deeply embedded and is probably the preferred choice.  There are reports that this RF radiation can cause DNA breaks and its attendant problems.

If they choose to go through the metal detector and trigger it, they are required to have a patdown in most locations. Choosing to go through the body scanner after setting off the detector is no longer an allowed option according to the TSA in 2018.

Spinal implants of the older type (screws and rods) are almost always a trigger to metal detectors and now we have new data that these implants can be a point source of heavy metal leakage into tissues.  This really concerns me in a 5G world and it is why this CPC is being released to you now 12 months before 5G becomes operationally globally.  Airports already are operating in 5G mode so this is why I focus in on travelers and it is also why I hate traveling now internationally.    For this reason I have told many of my older fusion patients if they want hardware removal as we go into a 4G/5G world I will now consider it for them.  I did not believe in previous years that the risk benefit ration favored patients but now I do.

These are mito-hacks few people consider today, but I have a sense in a 5G world they will become popular.  I believe it will be quite hard to find physicians willing to remove metal implants because they will not understand the bio-physical risks versus the medical bio-mechanical risks of the patient.  This means the patient will have to do their due diligence and make their own decisions that may be incongruent with their surgeons.

Internal metals likely will act as an antenna for the highly powered 5G waves.  I believe these patients might experience more autoimmune conversion, cancers, and electro-hypersensitivity.   The beauty of life resides deeply in bio-physics of materials and their interaction with light frequencies in the electromagnetic spectrum.

The secrets of life lies in the extent which seemingly complex and unrelated phenomena can be explained and correlated through a high level of abstraction by a set of laws which are amazing in their simplicity. Those laws are viewable to eyes who observe MRI’s daily; the wonders of the universe and of life are present in every image.  The key is learning to see what you observe in that picture or paying attention to patient complaints around their metal implants when 5G is operational.

We now have some data that placing a long titanium or metal pin down through the middle of a bone to stabilize it is linked with a much higher increase in the amount of metal ions found in the bloodstream. Chromium seems to have the highest levels reported for these intramedullary nails. Intramedullary titanium nails also increase the amount of titanium found in blood samples, but not as much as chromium. Evidently, the large surface area of the intramedullary nail exposes the bone to more titanium, thus the higher levels of serum (blood) metal. As a spine surgeon I used to never worry about this topic……now I do in a 5G world because if implanted metals leach inot the blood the radiation will affect the metal ions in our blood. I think the jury is still out on this but it is an area I am monitoring as network power density rises.

These 5G waves also have a topology that is very alien to humans and I have a sense that the topology and metals inside of us will lead to more mitochondrial diseases as time spent in these networks.  I go over that in both of the hyperlinks above.  Have a listen to them when you have a chance.  When you realize that 5G jump conducts to any conductor of electric or magnetic fields you will soon understand that this will make the time spent in the AC power grid is an added risk of metal implants in a 5G world.

CITES 

Detection of orthopaedic implants in vivo by enhanced-sensitivity, walk-through metal detectors. J Bone Joint Surg Am. 2007 Apr;89(4):742-6.

https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm559709.htm

https://sharylattkisson.com/2017/06/08/hidden-dangers-of-mris/

http://www.ncbi.nlm.nih.gov/pubmed/18819554

David G. Dennison, MD. Distal Radius Fractures and Titanium Volar Plates: Should We Take the Plates Out? In The Journal of Hand Surgery. January 2010. Vol. 35A. No. 1. Pp. 141-143.

 

Science gets interesting when you link it to life.  Recently on my Patreon blog, I have been linking a story of how deuterium links to life to make a difference in the reality we observe.  Deuterium is not a bad thing all the time.  In fact, when it comes to receptor biology, drug effect, neurotransmitter release, fecundity you begin to see there is no shortage of ways in which an extra neutron perturbs and helps life by altering the lifespan of a molecule.

This is why life is incredibly complex.  How a small simple change in a proton can really change many things we take for granted that bio-chemistry believes is true.  When you add a neutron to protons many things change in biochemistry in ways we fail to account for.  A two-fold mass gain decreases the bond length and increases bond strength. We fail to realize that temperature affects how hydrogen reacts hydrogen bonding networks suspended in an aqueous environment.

This ultimately changes a number of physical and chemical properties, including molar volume, polarity, electron donation, Van der Waal’s forces, dipolar moment, and lipophilicity. For example, deuterated caffeine is known to elute faster in the lab on a gas chromatograph mass spectrometer. This means this kind of coffee and can a much larger effect of caffeine on its adenosine receptors in the brain.  

 

 

This means deuterium in the wrong or right place in a molecule can change the reality of what could happen.

 

 

It appears the body has a tight quality assurance control program for how it uses and does not use deuterium over H+.  A coffee bean is a seed of the coffee plant and the source for coffee. Coffee is a C3 plant.  This means it has the most deuterium content based upon how photosynthesis parses deuterium using chloroplasts. Despite the classification as C3, coffee plants may display some interesting features concerning leaf anatomy and photosynthetic rates.  It is the pit inside the red or purple fruit often referred to as a cherry. Just like ordinary cherries, the coffee fruit is also a so-called stone fruit.  Fruits of plants are loaded with deuterium to control the growth of an immature plant into the adult form.

With deuterium laced coffee, a biohacker might even imagine trying to capture nature’s most elusive super buzz by drinking it and then turn around and sell that to an unassuming market to create a super addicting product.  The same is true for pills, Rx, and supplements and foods. In fact, depending on which of caffeine’s methyl groups were originally deuterated by the manufacturer’s processing, the cytochrome 450 enzymes that kick off its transformation in your liver (ultimately to formaldehyde) would likely balk at the enzymatically more resistant C-D bonds. This will delay the formation of some metabolites, creating a relative preponderance of others leading to effects that one would not see with standard non-deuterium laced coffee.  The coming age of quantum biology holds a cornucopia of effects we ignore today that have massive effects.  These effects can defy common intuition and common sense.

 

 

Did you know adenosine is the key signal for the human brain to enter the sleep phases where heteroplasmy rates are lowered? Did you know that heteroplasmy rates are lowered when we deuterium deplete our tissues? Did you know that deuterium is an isotope of hydrogen??? Do you know that the molecular formula for adenosine is: C10H13N5O4 Guess what happens if those 13 hydrogens are more deuterium and less H+?

You cannot sleep……..and the more of those hydrogens that are dueterium the closer you get to INSOMNIA and no ability to regenerate your tissues? You’ll believe you need a supplement pills the more deuterium you collect and you’ll get worse if you listen to them. Did you know warm water collected deuterium because of its kinetic isotope effect? Did you know coffee has caffeine in it? Did you know caffeine reduces sleep pressure (which is supposed to start low in the morning and peak shortly after sunset) and delays melatonin onset (Burke et al., 2015). Did you know caffeine is an adenosine antagonist? This means it ruins sleep! Could it be that caffeine in warm water increases deuterium content in the water you’re drinking while adding more adenosine molecules in your body ruining sleep? Could this be why people who drink a lot of coffee can’t sleep and think they need melatonin supplements to sleep too?

Just because you did coffee before without any issues matters little because you body has never faced the coming onslaught of 5G. That is why what you’ve done before as a mitochondriac might have to be completely retooled soon.

 

 

Did you know that the accumulation of adenosine loaded with protium and not deuterium in the brain throughout the day is thought to be a chemical mediator of sleep pressure? Did you know that caffeine use also delays and reduces melatonin action? Did you know melatonin pills augment the glycemic response in cells driving insulin higher and increase ubiqutin levels and leads to mitochondrial swelling? Did you know when mitochondria swell in your eyes because of the pills that it thins your retina? Did you know that in the AM nature says we’re supposed to have SUNLIGHT and FOOD not MELATONIN pills because the pills thin our retina and sunlight and protein thicken it and keep it normal?

 

 

Did you know a high protein AM meal optimizes the Vitamin A cycle in the retina? Did you know all opsin in the eye are bound to an retinol (Vitamin A)?  Did you know Vitamin A defects are associated with all diseases linked to a broken circadian mechanism?  Coffee is often associated with the development of adrenal fatigue by functional medicine docs on an adrenal stress index from a 0G-4G world.  How does this happen?  Adrenal fatigue links to the paraventricular nucleus in the brain (PVN). The PVN increases the sympathetic stress response.

Deuterium depletion is enhanced by the effects of high altitude and colder temperatures to stimulate heat release in mitochondria making high altitude (5000m >) glacier water some of the most naturally deuterium depleted waters in the world, with concentration levels between approximately 15-60 PPM.

You’ll notice when you embrace cold in your environment higher amounts of saliva produced after cold water immersion. Does it have anything to do with deuterium depletion or the autonomic nervous system? Yes, it does. With cold exposure you will urinate more.  If you checked the urine with a mass spectrometer you would see it had a lot of deuterium in it.  Why?  Urination is another parasympathetic process (vagal) because it facilitates heat release from mitochondria under cold exposure.   Heat stimulate cells to use H+ in their environments over deuterium.  The parasympathetic division of the autonomic nervous system functions with actions that do not require immediate reaction. A useful mnemonic to summarize the functions of the parasympathetic nervous system is SSLUDD (sexual arousal, salivation, lacrimation, urination, digestion, and defecation)

Sympathetic activation by using coffee can cause deuterium assimilation in the cytosol and matrix to affect the urea cycle and the TCA flux rate.

Light information is captured exclusively by the skin and eyes using specialized retinal photoreceptors and transduced directly to the SCN via a dedicated neural pathway, the retinohypothalamic tract (RHT).  The skin and retina use the same opsins to signal light information to the brain.  Each day the light-dark cycle resets the internal clock, which in turn synchronizes the physiology and behavior controlled by the clock.

The major biochemical correlate of the light/dark cycle is provided by the pineal melatonin rhythm. Under normal light-dark conditions, melatonin is produced only during the night, by using sunlight captured in biogenic amines during bright sunlight during the day to power the effect while ridding us of deuterium. Moreover, it provides an internal representation of the environmental photoperiod, specifically night length.

This pathways in the retina and skin also helps yoke the Vitamin A cycle in the photoreceptors to the environment in this way. Vitamin A and the B vitamins thiamine, niacin, and riboflavin are strongly fluorescent under UV light. This is why the B vitamins are used in the TCA cycle where NADH/NAD+ is a 340 nm fluorophore protein. These two cycles (Vitamin A and D) in the brain and skin become coupled correlated substrates that allow the brain to predict the future by trendsetting or ‘thin slicing’ light frequencies using photochemical cycles in out tissues.  It does this by ordering hydrogen into its quantum spin state.  Deuterium has a different spin number and magnetic moment and this is why it is handled differently than H+ under the power of sunlight.

Did you know coffee and melatonin pills ruin this coupling of melanopsin and Vitamin A in the retina and skin/fat?  Did you know it affects the neuropsin UVA receptor in your cornea and skin that link to Vitamin A?   Did you know a low melatonin level also cause an increase in heteroplasmy rate in the colony of mitochondria in you? Did you know the lower your melatonin levels the more you need sleep and AM sunlight exposure ? Did you know in the PM, if you have not experienced at least 8 hours of melatonin action on your mtDNA to lower heteroplasmy system wide, that more insulin MUST BE MADE? Did you know that excess insulin is not enough to maintain normal blood sugars? Do you think that is risk free?

SUMMARY

The risk benefit ratio for coffee is going to change in a 5G world.  In a 0G-4G world coffee could be thought of as a potential benefit.  In a 5G world it might be deadly because of the changes that a ruined circadian mechanism has on deuterium fractions in your mitochondria.  You need to consider that as the technology networks change around you. 

Today, coffee alone is a major cause of a circadian phase delay in humans. This should get you to realize that in today’s modern blue lit 4G environments that most of us should be avoiding a plant with high deuterium content.  Few of us live under the power of the SUN.  the sun depletes us of deuterium and blue light causes us to assimilate it.  Coffee has a positive vibe to it in our world.   Have you every realized that because of all of the above,  maybe why we think we need that coffee?  That need and desire is tied to how you use blue light and nnEMF to excess in your life.  5G is going to exacerbate this effect and not lesson it.

If you were wise,  you’d back off of coffee now before you are combating 5G in your hacks.

CITES:

http://www.scielo.br/pdf/bjpp/v15n1/a03v15n1.pdf

 

The Bohr effect hinges around the electromagnetic allosteric interactions between the heme molecules of the hemoglobin tetramer.  The Bohr effect a decrease in the amount of oxygen associated with hemoglobin and other respiratory compounds in the inner mitochondrial membrane in the cristae in response to a lowered blood pH resulting from an increased concentration of carbon dioxide in the blood.  Recall that in humans, CO2 levels, and not oxygenation stimulate breathing rhythms in the brain.

This effect is tied to a lowered blood pH (more acid = higher H+ or deuterium) resulting from an increased concentration of carbon dioxide in the blood.  As the exclusion zone (EZ) is built by the collision of sunlight with the water in blood plasma and in our cells, H+ is excluded from the quasicrystal lattice of the EZ,  and this increases CO2 to create headaches and cognitive decline in people.  This is why these symptoms are exploding now.  Most people live a life where too little sunlight is assimilated and this means the pH in the blood is no longer optimal.  The less sun you get the better your breathing mechanics must be to remain far from equilibrium.  This makes our cells act like a dissipative quantum structure.

HOW DOES THE POWER DENSITY OF THE ENVIRONMENT ALTER THE BOHR EFFECT?

The higher the power density of nnEMF/blue light is the more dominant the Bohr effect becomes.  As the Bohr effect becomes more dominant, it becomes the key etiology for keto- adaptation.  This is a false narrative.   Fat oxidation from a dietary change results in the creation of water and CO2 in cells and the blood.  We forget this basic physiologic fact of life.  So, when you go ketogenic by fat burning, it massively raises CO2 levels.  Those levels stimulate breathing more optimally.  This means if there is not a resultant CO2 spike in your blood with a dietary change you know you have a serious heteroplasmy rate issue in your mitochondria.

 

 

Cold exposure raises CO2 levels normally if mitochondrial function is decent.  If mitochondrial function is not optimized or you hack this in blue light you will notice higher spikes of glucose in your blood.   Moreover, the experience of the astronauts living in space, has taught us big time lessons.  In this environment,  nnEMF power densities is off the charts, it also raises metabolism of both fat and glucose simultaneously.  Blood tensions of CO2 are affected by the cardio pulmonary system or when mitochondrial metabolism is decreased and altered.  This is associated with an altered phosphate/oxygen ratio (P/O) and a lowered voltage on the inner mitochondrial membrane (called delta psi).  Since carbon dioxide reacts with water to form carbonic acid, an increase in CO2 results in a decrease in blood pH.  This results in hemoglobin proteins releasing their load of oxygen. Conversely, a decrease in carbon dioxide provokes an increase in pH, which results in hemoglobin picking up more oxygen.

H+ is hydrogen proton with its electron stripped.  Deuterium is a proton with a neutron in the nucleon with its electron stripped.  Both can act as a metal plasma in this state without their electrons.  The key difference between both is their magnetic moment.  We now know from research that the relaxation rate of water protons in a given tissue may become dependent on the interactions that ANY metal complex is able to set up with other substrates.   This is why we use gadolinium metals as contrast agents in MRI.  It turns out that deuterium can also act as a contrast agent in T1 imaging because of its kinetic isotope effect in hemoglobin.  This implies that deuterium content in our blood plasma may have a dramatic effect on how hemoglobin can operate to deliver oxygen and CO2 properly in humans.  Heavy deuteration from nnEMF power density would simulate pseudohypoxia in tissues in space or on Earth in environments loaded with nnEMF.  David Sinclair paper in December of 2013 linked pseudohypoxia to low NAD+ states and all diseases of aging.  This is consistent with what astronauts have experienced in space with regards to their health.  They all seem to age faster in space than Einstein’s law’s or relativity suggests.

The magnitude of the Bohr effect is usually given by the formula Δ log (P50)/ΔpH.  Hemoglobin can bind to oxygen and to protons as the video above shows.  What the video missed is the effect of deuterium replacement with hydrogen in their cartoons.  Why?  Deuterium has a much higher binding affinity to hemoglobin and to oxygen than light hydrogen does due to its kinetic isotope effect.

 

This means that the fractionation of H+/deuterium becomes very important. Recall that in space the an increased power density of nnEMF favors deuterium assimilation in our tissues over H+ assimilation for many reasons.

 

 

This will have a huge effect on how metabolism in mitochondria work and it will also effect temperature changes in the blood necessary for a proper melatonin cycle and cortisol cycle in astronauts.  These are the key features of why space travel is so dangerous to humans.

Here, P50 refers to the partial pressure of oxygen when 50% of hemoglobin’s binding sites are occupied. The formula is obtained by plotting the logarithm of this measurement on a graph at various pH levels, yielding a line with slope equal to Δlog(P50)/ ΔpH

Interestingly, Bohr effect strength exhibits an inverse relationship with the size of an organism: the magnitude of the Bohr effect increases as size and weight decreases (mass increase).  This has massive implications for humans with more mass from a higher deuterium fraction in their bodies compared on a relative basis with light hydrogen.

PROVOCATIVE SPECULATION

For example, mice possess a very strong Bohr effect, with a Δlog(P50)/ΔpH = value of 0.96, which requires relatively minor changes in H+ or CO2 concentrations to cause seismic physiologic changes, while elephants require much larger changes in concentration to achieve a much weaker effect  Δlog(P50)/ΔpH = 0.38.  This means mice will not tolerate space or high power density environments well, but fatter larger animals will.  Could this be why the obesity epidemic is really happening?  Might it be a protective mechanism to the amount of nnEMF we are using for communication?

 

 

The key point to understand is that any tissue or animal with a higher metabolic rate will be subject to the effect of deuterium to a much larger degree than we would expect.  This is why Scott Kelly had so many issues with cognitive function in space when his CO2 levels were pushed to the limit by the CO2 scrubbers used in the ISS.  It also underpins why his return to Earth has not gone well.

The Bohr effect is tightly coupled to metabolic scaling laws of Kleiber (mito matrix kinetics) but animals that eat a ton of DHA PUFA who inhabit cold environments tend to break these quantum rules we have seen in the literature.  So far NASA does not seem to realize the benefits of seafood for human space travel due to the power density effect on the Bohr effect.

WHY IS SEAFOOD PROTECTIVE TO nnEMF?

An exception to the otherwise well-supported link between animal body size and the sensitivity of its hemoglobin to changes in pH was discovered in 1961 in sea mammals.  Based on their size and weight, many marine mammals were hypothesized to have a very low, almost negligible Bohr effect. However, when their blood was examined, this was not the case.  This allows them to get rid of all their oxygen when they dive deep in water when oxygen is not present.  We know water is a natural Faraday cage and it transfer heat 24 times more than air does so this likely causes them to be the exception rather than the rule.  The cold anoxic environment are stimulating physiologic changes to make their hemoglobin hold onto oxygen with more affinity than would happen in air.  Cite 3 below goes into the complex chemistry why this happens.   This is why humans might want to keep a body of water close to them in a 5G world while doing their hacks or exercise.  They can use this effect as 5G takes hold.

Another special case of the Bohr effect occurs when carbon monoxide is present in the environment or tissues. This molecule serves as a competitive inhibitor for oxygen, and binds to hemoglobin to form carboxyhemoglobin. hemoglobin’s affinity for CO is about 250 times stronger than its affinity for O2, meaning that it is very unlikely to dissociate from Hb, and once bound, it blocks the binding of O2 to that subunit.  Methylene blue is very helpful in carbon monoxide poisoning just as it is helpful in heavy deuteration in the mitochondrial matrix.  CO acts with O2 in a very similar way that deuterium does with oxygen via its kinetic isotope effect.  D-O bond is 10.6 times stronger than the H+-O bond.

How does cold improve immune regulation??? One fallacy I’d like to slay from the Internet is that it is brought on by breathing pattern. This is a false narrative built by Wim Hoff. It works on a bio-physical mechanism within the WBC’s which are normally loaded with deuterium to help boost immune response. This means that WBC have more deuterium in them to raise temperature to affect immune function and proton flows.  So today I’d like to give you education on both sides of the equation. I truly like Wim Hoff and I love that he brings humans back to nature in the cold I just am not in love that he has no earthly idea why what he does works.

Wim apparently doesn’t know:  that heavy “in and out breathing”, as he teaches is beneficial.  It is not.  This method significantly reduces carbon dioxide in the blood making blood more alkaline and that hemoglobin in alkaline blood has a harder time releasing oxygen to the tissues than in normal blood (which is slightly alkaline).

Due to the Bohr Effect, hypocapnia causes cerebral hypoxia which sounds dangerous and opposite to what Wim Hof states in his classes. It causes headaches and cognitive haze that submariners and astronauts get.  Just two parts per million increase in CO2 can cause this in space.  NASA uses 2 ppm for its CO2 scrubbers and cosmonauts use 6 ppm for their scrubber’s causing problems for astronauts who return from the ISS in a Soyuz space capsule like Scott Kelly did last year.  This is why cosmonauts use much less water during re entry and take a ton of salt instead.  Astronauts drink a ton more water with salt but they need to rely on wearing a diaper during re entry because of the fluid shifts that occur when they come back into gravity and inside the magnetosphere from the vaccum of space.  Ironically, this difference in technique between space workers in Russia and the USA is a big tell why some people urinate too much at night and those who do not.  Wim’s breathing technique resembles what Kelly faced in his space return and also sounds similar to the childhood fainting game that aims to create euphoria or giddiness.

In humans, the primary urge to breathe comes from CO2 receptors in the brain when they sense that there is too much CO2 in the blood.  We are very sensitive to this and become more sensitive to CO2 when our cell membranes are DHA deficient.  It turns out we know that deuterium also cause massive turnover of cell membranes and depletes of DHA as well.  This maybe the key reason why seafood is irreplaceable in a 5G world.   It also maybe why NASA is now pushing its astronauts to take DHA supplements with them into space.  So far the supplements have not helped and I have a sneaking suspicion why is related to the deuterium content of the fish oil when it was manufactured.    Wim happens to be a vegetarian and a smoker.  Therefore he has little DHA and lots of CO in him.  This state is not the state of most of his clients and not too many of them know it.  This is why I would never go train with him.  I choose to do it the way nature built us to work.  But it does point out one great thing.  Cold is massive helpful to humans living on Earth surface now in a 4G world.  Wim gets this one very correct.

 

Therefore, being able to maintain a long breath-hold after heavy “in and out breathing” doesn’t mean that the body has been flooded with oxygen; instead the ability to have a long breath-hold is primarily because the urge to breathe has been lessened due to low CO2 signal in the blood. How cold immunity works is linked to deuterium motions between immune cells and blood plasma.  Moreover, it is related to the fact that immunogenic proteins in us are reacting to the power density of the environment around us, and this is what activates epitopes inside of us to increase immunity or decrease immunity.  This is why the power density increases of today are linked to autoimmunity and to autism in my humble opinion.

When you know better, you can begin to do better.

CITES

https://www.nature.com/articles/s41598-017-11288-9

https://www.ncbi.nlm.nih.gov/pubmed/23430994

https://www.sciencedirect.com/science/article/pii/S0006349599774266

Scott Kelly.  “Endurance”. My one year in space.  2017.