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–ketosteroidshave 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:
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.
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.
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.
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.
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 normalkidney 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.
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.
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.
I have a sense when 5 G is released this blog will be the most important one people will search. Why? In it has most of the key mito-hacks that one will need to consider to offset electromagnetic diseases linked to 5G exposure.
Blood is magnetohydrodynamic fluid. What does this mean to the ‘mitochondria’?? Oxygenated blood is repelled by the magnets. This means oxygenated blood is diamagnetic within the hemoglobin molecule.
Diamagnetic materials are repelled by a magnetic field; an applied magnetic field creates an induced magnetic field in them in the opposite direction, causing a repulsive force. You saw this visually above. Water is a diamagnetic material. It makes up 93% of blood. Superconductors are considered perfect diamagnets (χv = −1), because they expel all fields (except in a thin surface layer) due to the Meissner effect. When water ‘gains the ability‘ to absorb more electric or magnetic flux from sunlight it becomes like a superconductor. This helps man when he steps barefooted on Earth and when his surfaces are exposed to the sun. The result is always seen in the shape of the curve of his cortisol and melatonin curves on an adrenal stress index.
People in medicine now know that children have an innate advantage to remain healthy and young because their blood is MORE magnetically sensitive to sunlight and to a connection with the planet. This makes it more able to bond to oxygen and deliver oxygen to mitochondria. This is the basis of all parabiotic studies. Blood transfusions from younger people are beneficial for oxygen delivery. These abilities are linked to size and shape changes in red blood cells (RBC’s) that have specific names tied to altered cell membrane changes.
Shape variations of RBC’s are known to occur upon exposure to various drugs (MB) or under diseased conditions. The commonly observed shapes are called discocytic, echinocytic, and stomatocytic.
Echinocytes in human biology, refers to a form of red blood cell that has an abnormal cell membrane characterized by many small, evenly spaced thorny projections as the arrows below show.
Echinocytes in human biology and medicine, refers to a form of red blood cell that has an abnormal cell membrane characterized by many small, evenly spaced thorny projections. The liver is the organ Dr. Doug Wallace has likened to the sun inside the human system because it is a giant hydrogen fuel source. Echinocytes are found in hyperlipidemia caused by liver dysfunction, because the lipids themselves do not integrate into the membrane. It appears the electromagnetic foot print of the environment is magnetic stored in the HDL/LDL level of the blood plasma. High HDL levels tell us that our liver and blood can harness more magnetic flux from the sun via the sun by way of the skin and eyes. IT appears that cell surface receptors on the red blood cells bind with HDL cholesterol which induces the shape change of echinocytes.
These cells have been also shown to develop in vivo during human hemodialysis. They disappear immediately at the end of the procedure. The level of echinocytosis appeared to be related to the increase in blood viscosity that occurs during hemodialysis. This tells us that dialysis at its core is an electromagnetic treatment. Most nephrologists appear to be unaware of this. A quantum clinician should be aware of it. Dialysis might be a key treatment in a 5G world. Adding a teenager blood during the treatment will extend the effect.
The formation of echinocytes is seriously determined by electric field pulses from the environment. Why do I have a deep disdain for Tesla? AC current are devastating to blood cells and this is why the power grid exposures are linked to so many leukemia’s and lymphoma’s. This was the basis of Dr. Judy Wertheimer’s studies mentioned in Dr. Becker’s books. Alternating electric current produces modifications in the membranes of red blood cells, attributed to a higher permeability to water and a decreased tonicity, leading to the transformation into echinocytes. This is why excessive use of salt, and DDW water might be a key strategy in a 5G world.
The discocytic RBC’s can be transformed to echinocytic or stomatocytic shape under different electromagnetic conditions in the environment. This has huge implication to the quantum clinician. We can see the evidence of redox changes in mitochondria in patients by knowing what to look for in their RBC’s morphology. This is evidence of a change in their redox potential and the zeta potential in their blood. Right now only dark field microscopy has made a presence in medicine, but this is a very crude way to tell the clinician about changes in the viscosity of blood and changes in the electromagnetic potential of platelets and RBC’s in the circulatory system. There is a better way to examine blood that I believe will become imperative in a 5G blue lit world. The use of Raman spectroscopy will become very popular in future virtual private hospitals run by quantum clinicians because of the information in this blog.
The Raman spectra of the three major shape variations, namely discocyte, echinocyte, and stomatocyte, of RBCs were studied while subjecting the cells to oxygenated and deoxygenated conditions. Analysis of the recorded spectra I’ve examined has suggested to me that an increased level of hemoglobin (Hb)-oxygen affinity is present for the echinocytic RBC’s. Also, some level of Hb degradation can be noticed for the deoxygenated echinocytes that develop in an environment with high power density. The effects may arise from a reduced level of intracellular adenosine triphosphate in echinocytic cells and an increased fraction of submembrane Hb. This tells us that electromagnetic power density is being sensed via our blood cells and water in our blood.
Metabolism in a tissue creates a change in the magnetic flux in tissues. This is the quantum clue that blood uses to operate in us to bring sunlight and oxygen to mitochondria struggling to breathe. As metabolic rate rises more oxygen is needed and the ATPase must spin fastest. This means oxygen tensions and deuterium fractions in the mitochondrial matrix are quantized to solar exposure of our skin and eyes. This metabolic increase in our tissues will require additional oxygen. Therefore, there will be an increase in oxygenated blood flow (oxyhemoglobin) to the local brain area that is active. Oxyhemoglobin differs in it’s magnetic properties from deoxyhemoglobin. Oxyhemoglobin is diamagnetic like water and cellular tissue.It seeks out mitochondria with lower magnetic strength. This means the ATPase Fo head is not spinning enough to make enough ATP. This lowers the P/O ratio and draws oxygen rich blood to tissues with diminished mitochondrial function. These mitochondria would be described as pseudohypoxic. Pseudohypoxia is a phenomena that expands in natural aging as mitochondrial function declines. As this happens NAD+ decreases compared to NADH levels at cytochrome 1 because not enough protons are being moved from the matrix to the outer membrane space in mitochondria as the Fo head spin rate slows for any reason (ie:deuterium fractions increased). De-oxygenated blood attracts the magnet. This means that de-oxy hemoglobin is more paramagnetic in blood returning to the heart. As blood loses its electromagnetic capabilities the results are seen in our arterial walls and the levels of nitric oxide we release.
Ask yourself why nature would build life this way? Where are the magnets to draw venous like blood? Those magnetic fields are in the mitochondria of the heart. The most mitochondria in any tissue is located in the heart. Second most common density is found in the brain. Oxygen comes to us from our lungs. Oxygen is paramagnetic atom on the periodic table. The reason that it is paramagnetic is because the oxygen molecule has two unpaired electrons in its valence shell. This means de-oxy blood has this atomic arrangement in hemoglobin. Electrons not only go around the atom in their orbitals, they also spin (quantum spin), which creates a magnetic field. Unpaired electrons spin in the same direction as each other, which increases the magnetic field effect. We use this effect in neurosurgery when we use a test called BOLD for functional MRI scanning. BOLD is a contrast we use to develop proton images in MRI. Deoxyhemoglobin is due to 4 unpaired electrons at each iron center.
The presence of paramagnetic deoxyhemoglobin within red blood cells creates local magnetic field distortions (susceptibility gradients) in and around blood vessels that create electric and magnetic fields within the blood vessel to provide and electromagnetic stimulus that precedes physiologic changes in the circulatory system. As the cell membrane changes in RBC’s so does the quantum actions in the pi-electron cloud of DHA in the RBC membrane. This underpins the size and shape changes in RBC’s in animals.
SUMMARY
Under physiological conditions, a normal human RBC assumes a biconcave discoid (discocyte) shape ≈8 μm in diameter. It has been known for more than 62 years that a variety of agents can modify this shape systematically and reversibly at constant area and volume.
One set of agents, including anionic amphipaths, high salt, high pH, ATP depletion, cholesterol enrichment, and proximity to a glass surface (hydrophilic), induces a series of crenated shapes, called echinocytes, characterized by convex rounded protrusions or spicules. Under further loading, the spicules become smaller and more numerous and eventually (in a process that we shall not discuss further here) bud off irreversibly, forming extracellular vesicles composed of plasma membrane materials and leaving behind a more or less spherical body with reduced area and volume (the spheroechinocyte).
Another set of agents, including cationic amphipaths, low salt, low pH, and cholesterol depletion, induces concave shapes called stomatocytes. On further loading, multiple concave invaginations are produced, which eventually bud off to form interior vesicles and leave a spherostomatocyte.
This “main sequence” is universal in the animal kingdom in blood in the sense that the shapes seen and their order of appearance do not depend on which echinocytogenic or stomatocytogenic agent is used. Other shapes outside of this main sequence are also seen under certain conditions related to the electromagnetic environment. More than likely these initial electromagnetic changes are likely precursors to methylation changes in DNA and RNA we’ve now see in astronauts twins. (Scott Kelly)
This video is one of 4 filmed in March of 2015 in New Orleans for the movie Unbound. My part in the movie was cut down to about 15 minutes so we have lots of footage left over. I asked the movie patron, Ruben to release to me some of the footage so I could share it with you as webinar events. He agreed. Here is the first we got. It shows us heading to my spot on the Mississippi River levee just before sunrise in March. Ben Smith was the movie maker and some of the images in this clip as the sun is moving across the sky and on the church were spectacular.
LIGHT IS THE ULTIMATE ENERGY STIMULUS TO LIFE
When light is slowed down we can then use processes in nature to make things with mass with its energy. This is exactly what photosynthesis does.
Most modern technology works electronically by using light to make electrons do the things we want them to do on semiconductors. All electronic semiconductor circuits work on the basic idea that any given electrons can influence the control of other electrons and holes adjacent to those electrons using light frequencies. This implies that we can use light or the current in a light’s waves to control another current in a specific way we want to engineer to gain an effect. That is what a transitor gave mankind in the technology revolution. 650 million years ago life harnessed this control using chloroplasts to make the entire food web. This is what me and ruben were discussing as we left my house and headed toward the River. Without capturing the sunlight’s power and turning it into mass, life could do little physiologic work. This is why for 3.8 billion years life was somple in two domains.
Once light was captured in things with mass the food webs were born. C02 and water were brought together using the sunpower in a chloroplast to make foods. Foods are sunlight coded for in a mass form.
It took us 50 million years for the living system to reverse the photosynthetic reaction. Here we took the energy and information in food mass and turned it back into energy. Our mitochondrial matrix turns glucose and fat back into CO2 and water.
WATER: Captures both electric and magnetic fields from light to power life. The key for water is its location not its quantity or quality.
Most people wrongly assume the Earth is a water filled planet but that is a big misnomer. Earth is an oxymoron. It is an ocean planet that is bone dry. The oceans have an average depth of 4 kilometers and they hold enough water to fill a sphere more than 1300 kilometers across. That is it. 2/3 of Earth is covered by water from a space view, but many people are surprised to find out that all of this water only forms 0.02 % of the mass of Earth. For analogy purposes, if our planet was a 300,000 kilogram Boeing 777, then all the ocean water’s mass would equal would be the mass of one passenger on this plane. That is how rare water really is on Earth. What fools us to this reality is the location of water. It is on the surface where we can perceive it, giving us the facade that water is abundant. It is not. But its location is the key to why Earth can foster life using sunlight. Water forms our skin on this planets’ microbiome. Freshwater is mainly locked up in the polar icecaps, clouds, lakes, soils, and the Earth’s biota only makes up a tiny fraction of this total. That is how rare your water supply is. The one made in your mitochondria is even more rare because of how it is made.
MONUMENTS OF CHANGE: IDEAS
Ideas can change everything about us when they are focused on things that matter to nature.
In the video Ruben asks me about different philosophies and how they tie to my ideas. I mention to him immediately it is akin to how light collides into matter to make new things entirely. I am not so sure he understood what I meant but I laid that thesis out completely in my Vermont 2017 youtube video. Remember this footage was done long before that meeting.
CHANGE WITHOUT CHANGE:
Can be done by things using light as its “middle man” because light is all energy and not encumbered by mass. This means it is the point source of how matter changes by non linear mechanisms. That a small stimulus packs a large punch to cause creation of things we can rarely fathom.
For example sunlight drives viral amplification in the seas, and that amplification drove evolution by amplifying the genome. This could not occur if the sea was buried in the mantle. It could occur because the sea water was on the surface where light could collide with it.
Viral genomes crafted in seawater can permanently colonize living systems who consume these particles. The viral genes can enter their hosts genomes, adding data and information to host lineages. Sunlight hitting the sea every AM is capable of this quantum mechanism and no one appears to see it, but science knows it happens everyday the sun rises. Some living systems will see massive alterations to their sturcture because of the infection, and its effect will be reflected in their ancestors genomes. This is seen in our haplotypes as we migrated around the Earth by waterways. What variable in water varies by latitude and solar exposure? Deuterium content of the water that living systems use is what causes variation.
Most viruses are co-apatative and adaptive to a new environment and now that we are in the era of genomics, we have definitive proof that viral imprints and remnants are present all over the human genome. They are present in all domains of life and the past evidence of viral colonization is the baseline of life and not an exception. Why do ignore it? Change without change. We do not appreciate that sunlight frequencies drove these changes in water as we moved across the planet.
All living things are built to be susceptible to viral elements for a quantum reason. Change without change is the reason behind this effect. This mechanism blinds us to what is happen at the smallest scales in our cells. It becomes the “casino dealer” inside of every cell for environmental changes that have occurred on this Epi-paleo blue dot.
The genome is an ‘organ of the cell’, not its dictator. The matrix thermodynamic abilities during this migration set how much energy the living system could make from foodstuffs, water, and sunlight as we moved.
Genes don’t have this free will. Something must have forced them to misbehave: altered light frequencies were the prime mover of change.
The gene does not lead, it follows. What does it follow? The electromagnetic force of the universe in that part of the environment the disturbance occurs in .
Today, treatment guidelines are often based on outdated evidence, turning evidence into harm. Doing no present harm is what should drive consensus as man has altered his environment, but this though never occurs to our species because we are ignorant to how we came to be.
Wisdom allows great people to become small, to understand nature’s complexity. Nature hides her best recipes from us because the laws of quantum mechanics dictates she must.
When water is heated water under goes a blue shift. The more water is heated the more deuterium it acquires because the DDW is evaporated. When water is cooled water undergoes a red shift and its density and viscosity shift changing its magnetic and electric abilities. This gives water a doppler effect with respect to temperature, to determine flow and direction. This is why all living systems have heat that flows from hot to cold even though there is no universal law that predicts this flow pattern.
Water molecules can surround the ions in solution and effectively neutralize charges just like the magnetosphere does to sunlight on Earth. This makes water in living systems a type of magnetohydrodynamic plasma. This plasma can carry more electric and magnetic energy from sunlight when deuterium is removed from the water. So sunlight needs to use the cells in blood and the 93% water it contains to carry electric field and magnetic field energy to keep us healthy. The parabiotic studies of transfusion of blood from young to old mammals is even more intresting. I believe the reason why young blood favors youthful presence in the redox potential of tissues is because it is more deuterium depleted. The quantum mechanism built into this process work better with blood cells that are younger because they are more efficient at turning sunlight into electric and magnetic flux in cells.
Then the quantum dance gets more interesting: Our blood plasma is designed to be infused with the rapture of solar plasma that never shows clinicians what is really changing in it fundamentally into something that keeps us young. If our labs did allow this observation, it would never occur because of the Zeno effect. So nature, keeps us “in the dark” by design, as ithe sun burns wellness into you, for your tissues, while an audience of people and physicians are watching it all unfold but have no clue at what is really happening. What is the observer in our living state? The amount of deuterium on the surface of our DNA and RNA is the observer of this effect. The amount of deuterium and its location is critical in deciphering the optical data.
DNA decreases the hydrogen bonding network in cell water freeing up deuterium from RNA and DNA surfaces. UV light orders the water molecules by increasing the hydrogen bonds in water and creating a larger exclusion zone. This water excludes everything above the size a proton (H+). This is how the body rids itself of deuterium. Might the reason all cells release ELF-UV light is this is the core mechanism of how we free up deuterium for removal from our tissues? Yep.
I’ll never tell you what to do, but I will always remind you of what you already know, and help you reconnect to that wild intelligence that resides in your DNA/RNA. We know from experiment that nucleic acids liberate ELF-UV light.
Dermatology and Ophthalmology riddle: If UV light is so horrible for biology and cells ask your skin and eye doctors to explain how DNA has been shown in thousands of experiments to have a spectrum of fluorescence peak at 350 nm? That peak is 100% in the UV range, FYI. Then ask them why the two proteins that are tightly associated with DNA, histones and chromatin, both have been found by experiment to delay this UV light release in DNA in all normal cells? So this means when DNA/RNA are unwound to be transcribed, ELF-UV light is liberated. Why would nature do this? Is this how she sheds her excess atomic mass?
Nucleic acids, like DNA/RNA have chiral centers. The only amino acid that is achiral is glycine. For example, in DNA the atoms C1′, C3′, and C4′ are chiral, while RNA has an additional chiral center at C2′. Chirality is central to all molecular interactions in biological systems. It turns out this chirality is also key to where a cell will put deuterium on a carbon in nucleic acids. It turns out it is not a random event as Darwin wanted us all to believe. It is quite specific and calculated by the power density in solar rays. This process is quantized. A simple experiment demonstrates the principle: try to shake someone’s left hand with your right. It cannot be done because of this structural specificity. All DNA/RNA absorbs light but scatters most of the energy in it. This means RNA and DNA dissipates light energy too and we fail to account for it.
The key is transforming the environmental energies to something different and new using the light of the sun……….We are all made up of carefully broken pieces of carbon mass from the food webs and out mitochondria are the glue that make life work by using energy to make “these masses” operate in the environment our cell senses. This is why I call a cell a playground for photons. Cells have to get information from the incident EMF light ray to know what kind of signal to make with it. This is why certain free radicals are made by certain light frequencies and not others.
Now lets have a look at what happens when we move deuterium around in our nucleic acids……..Are all the positions in the ribose ring equivalent from an energy basis? Nope.
Where deuterium is in RNA and DNA tells us how much light energy can be dissipated by the nucleic acid as the pictures above show you. The position on the ribose backbone is not equivalent for any carbon in that ring. This follows the idea that the amount of deuterium in the matrix determines how much energy is available to the living system at any particular time……….that is what heteroplasmy is in a nutshell.
When you have a relationship with a friend, a lover, family member, whenever you sample their ELF-UV light from their touch, DNA, or their face or skin you can sample the degree of entanglement to know something deeper about that person. The more your particles are entangled with theirs, using light photons coming from your bio-molecules the more connected you become to them in ways you cannot fathom. That is the essence of the Quantum Zeno effect. You are not meant to observe how we all connect to other things in nature. This light also links all of our colonies of mitochondria in our tissues together to work as a team.
When you are going through something hard in life, like illness, and wondering where Nature is in the process, remember the teacher is always quiet during the test ……that is the essence of understanding the quantum zeno effect. What are the missing keys to humans? The teachers who remain quiet to us: the Sun, cold, grounding, and proper Schumann signaling in the ionosphere.
Each one forms the basis of the circadian mechanism in your life that allows you to collect the proper EMF’s from the Earth and Sun and avoid the collection of deuterium from the non native EMF’s on this planet. The better the connection the more wellness we get. That fidelity is the reality of how the system works. This raises an interesting point as you watch the video: What is evolution to a mitochondriac?
Evolution:
It does not mean random
It does not mean to improve
It does not mean morphing during a lifetime
It does not mean abiogenesis
It does not mean the origins of the universe
It does not mean social Darwinism
It does not mean amoral
It does not address theologic claims
It does not mean atheism, communism, racism or any ideology
Evolution means change over time brought about by environmental change
You may not perceive it with your rudimentary senses but your mitochondria does.
If you deny that things: The universe, change over time, then you deny reality.
That theory of biological evolution attempts to explain the facts and connect the data that indicate that life on earth is related through a common descent and has been changing for a long time.
Ask yourself this: what are the implications of a decline in viral ERV integration in our species’ genome over the millennia? The placental ERV allows a child to sample his mother’s blood and do it safely by guaranteeing pregnancy has a Th-1 immune response. When you lose that ability then the zygote is at an energy deficit and it increases their % heteroplasmy right off that bat and you can ruin the imprinting of the epi-genetic marks (deuterium in methyl or acyl groups) that were present in the mother’s germ line for generations.
ARE RCT’s A REAL GOLD STANDARD WHEN YOU CONSIDER QED RULES?
No, they are not the same because they do not have the same goals. Biology tells us that a RCT is the gold standard when the laws of physics tells us the opposite. Things do not happen over and over again when an environemnt varies. This is why RCT’s in medicine are wholly a waste of resources. It follows that undrstanding how energy flows in a system is the only way to understanding true cause and effect in a living system.
In other words, cellular organization is the most critical part of life, not the fuels we put into it. The environment the cell is in, is sensed by our mitochondria, and this determines the organization of the cell. This makes our mitochondrial physiology a mirror image of the present environment and how much energy the cell can make right now. In today’s microwaved blue lit environment, that ability has altered our mito-chondria to “cyberchondria“. Cells cannot make the energy needed when the ionosphere is now chronically overpowered with other parts of the light spectrum.
SPHINXING: Early March in NOLA we can make Vitamin D at 8:17 AM at 28 North latitude.
1965 Noble Prize: Schwinger vs Feymann both got because somebody else proved both explanations were identical using math.
Coherent domains in water : lack of deuterium = water a plasma
Light has massive amount of frequencies to control the 100,000 biomolecules that act per second in a cell. Solar light is used to power up electrons and move protons and these electrons have to get assigned a quantum spin number in mitochondria. It turns out mitochondria favor the quantum spin number of protons from nature too. So light acts as the currency in the compound pharmacy in our pituitary and circulatory system every day to make things we need from light. If you understand factorial math, that means within our single octave of the visible spectrum that retinal cells, skin cells, and water in our circulatory system that control bio-chemicals can handle 8,683,317,618,811,886,495,518,194,401,280,000,000 different frequencies. That is how many are present in our tissues optical windows from 250nm-780nm. Each frequencies is coded for each codon present in our nucleic acids and in bio-molecules in cells. This number shows you how solar light offers cells a staggering level of power and control. So when you open up any biochemistry book and realize that biochemistry only uses 100,000 substrates in reactions per second you realize light can control them all with easy. When you factor in that light light works photoelectrically, and that the photoelectric effect acts instantaneously, with no time delay, then you begin to see how 100,000 biochemical reactions can occur per second using light frequencies from the visible spectrum easily. These frequencies also are what build the coherent domains and redox pile of electrons that control life’s Jablonski diagram.
Coherent domains in water’s hydrogen bonding network are pieces of matter with specific masses that effects energy and it conversion. Energy is neither created nor destroyed. It just changes shape. Energy and mass are both one and the same thing……….the field around them dictate their state and conversion = mass equivalence of Einstein.
Coherent domains in water = instantaneous changes in size and shape of water molecules to incident light, electric fields, its magnetic field, or nnEMF or blue light. With technology, we’re waltzing with the wrecking ball today, because this creates waveforms in our mitochondrial matrix that feel like we are no longer on our home planet anymore. The more deuterium we get into our CSF the more depressed we get. Isn’t it funny how every plant in the solar system has a different deuterium footprint in its crust? Do you think this atomic signal was not important in building a mitochondria at some level?
Coherent water = exclusion zone (EZ). EZ’s can vary in size and shape depending upon the substance and the amount of light entering the water. Liquid water is therefore a multi-fluid system in a cell. It is very dynamic because light frequencies dictate that is how it must work. It is in its bulk state with deuterium) when it is not touching hydrophilic proteins and not in light. This is similar in analogy with superfluid helium in cold or heat. Bulk water consists of a coherent phase which is about 40 percent of total volume at room temperature and an incoherent phase 60%. I believe it is not 100% because of the effect of deuterium in this volume of water. In the coherent phase only, the water molecules oscillate between two electronic configurations in phase with a resonating solar EMF. I believe coherent water is essentially DDW or devoid of it in some cases. In nature, that incident EMF should be the sun and/or the Schumann depending upon the presence or absence of light during the day.
The common frequency of the EMF and the electronic oscillation of the coherent phase being 0.26 eV; whereas the energy difference of the two electronic configuration of the coherent phase is 12.06 eV, which gives the wavelength of 1000 A (100 nm) of the coherence domain. The remaining 60 percent of the incoherent phase is extracted by thermal fluctuations (eddies) from the coherent phase. So the types of EMF’s can really mess with water composition inside of living systems and show how big a chameleon water really is when it changes by the power density in light. The two phases have widely different dielectric constants: Bulk water is 78. Coherent water is WAY higher (160). This is why electrons and photons from the sun make water supercharged when it is DDW and irradiated between 250nm-780nm. The coherent phase is 160, due to the high polarizability of the coherently aligned water molecules that are oscillating in concert; while the dielectric constant of the incoherent state is about 15. 160 +15 = 175. Divide by two and you approximate 78 which is what you see published………on bulk water. Nobody breaks it down like this because no one sees water as I do………it is life’s version of a superconductive superfluid on Earth like hydrogen is in th esun or helium is in a MRI machine.
Coherent water = EZ = magnetohydrodynamic fluid of immense ability to make quantum computing possible. Most of our brain is water. IT is surrounded by water in the form of CSF which is DDW as well. The externally applied electric fields are only felt in the non-coherent phase because sunlight can affect the 40% coherent phase to alter the 60 % depending upon the environments our choices make. This is why the DC electric current is operational in wakefulness and vanishes at night. Just when you think you know water…………you begin to realize you don’t know it all. This is why medicine struggles to explain life. Not only is water stranger than we think, it is stranger than we can think about it. I personally think nature’s imagination with respect to water’s abilities is much greater than our own imagination. This is why I mentioned the water researchers in the video and compared them to the two sceintists who shared the 1965 Nobel Prize. Nature is never going to let us relax because of how she shape shifts hydrogen in water to create life’s magic using light and magnetic flux.
Any time light changes to mass certain specific things happen quantum mechanically. Anytime this happens biologically you can bet the Warburg metabolism is also present for a deep physical reason that is contrary to the paradigm belief. Any cell that loses sensory confinement must exhibit this specific form of metabolism because this form of metabolism because of how light released best by a eukaryotic cell to be transformed into matter or transform the atomic mass in our tissues. This becomes a huge deal when our deuterium fractions are higher. Dr. Vander Heiden’s lab is now pursuing a more comprehensive understanding of how the Warburg effect may help cells reproduce. This lab is very close to Ruben in Boston. The lab is trying to refocuses the question, on whether the redox shift in out matrix is truly pathologic or due to changes in dynamic energy flux in the environment the matrix senses via water networks. It isn’t necessarily about how the Warburg effect helps cells put glucose into cell mass, but more about why does glucose-to-lactate conversion help cells use amino acids to build more cells that might be key. I think he will find it is all related to controlling proton spin numbers in the matrix to match up to the environments thermodymaics to the tissues ability to make energy in this environment. I am guessing what he will find………mitochondria have chosen to use red light or heat for one physical reason……..it confines light in a cell’s water. This is wht water has a massive heat capacity. ELF-UV light to be used specifically because UV light offers non linear stimulus to cells. I believe ELF-UV light is how we remove deuterium from the cells, blood plasma, and CSF at night.
UV and IR light and cold are a medical solution for medical reversals.
Cold water immersion at 14°C increased metabolic rate by 350%, norepinephrine by 530% & dopamine by 250%. Wow. How did it occur? Cold selects for protium and we urinate out deuterium. This is exactly how a ketogenic diet works in cold environments and protects us from mitochondrial disease and the effect of the increased atomic mass in our matrix. It is in fact, how Gleevac,a cancer drug, mechanistically works in Chronic Myelocytic Leukemia. Most clinicians have no idea why though it can happen. It all ties back to the coulomb interactions (charges) in our tissues and inside the mitochondrial matrix. Charges always link back to light and temperature changes in tissues. http://www.ncbi.nlm.nih.gov/pubmed/10751106/
Cold also depletes us of deuterium. You do know cold increases magnetic flux because of the Curie temperature relationship right?? Might this be the missing link for how magnetic field strength could help clear our tissues of deuterium? Is this why Jack tries to lure us to the crater every NYE in Mexico? IS he trying to show us how nature really works without telling us so we begin to understand how the Quantum Zeno effect is operating like the wizrd behind the curtain in us?
When you lose ELF-UV, you are losing your life force because more deuterium remains in the system and as result, our mitochondrial swells and we release light from cells. this causes the mitochondria to swell and shape change and increase volume which is the main stimulus a cell need to generate a chronic pro-growth bias to lead to cancer. Pressure builds heat = why free diving works in poorly function mitochondria to a degree.
Heat expands most things in the universe but one thing it does not at small scale. And we all need it to live. Cell water from the matrix. I believe this is why mitochondria have chosen to release heat dynamically via our haplotypes for one reason……………because heat shrinks DDW and shrinking water around your ECT breaks nature symmetry by shortening the distance of the respiratory proteins on ECT. This increases energy production from ECT and the amount of H+ over deuterium in the matrix to make energy………this is why fish swim below ice, and why icebergs float on liquid water, and how and why mitochondria make DDW and heat to confine light using the electric and magnetic charge in them. Kruse Science 101.
These where the ideas I was trying to get through to Ruben on that March morning at the River. When you read my words and juxtapose them over this edit cut……..what do you see now, you missed before?
Parting shot: 5G will be the worse thing to hit Earth since the asteroid 65 million years ago hit Mexico. Contemplate that now.
MELANOPSIN COUPLES TO VITAMIN A, SO ALL CIRCADIAN DISEASES CAN BE TRACKED BY ALTERATIONS IN THE RETINA FOR MOST DISEASES IN BIOLOGY
MELANOPSIN HAS BEEN FOUND TO BE PRESENT IN THE SUBCUTANEOUS FAT MASS OF HUMANS…….WHAT ARE THE IMPLICATIONS?
3. ALMOST ALL OF THESE EFFECTS CAN BE TRACED BACK TO THE RECYCLING OF PROTONS IN TISSUES
In humans, melanopsin is expressed in a small subset of cells representing only 1–2 % of all retinal ganglion cells (RGC) in the retina. These photoreceptors measure the intensity of light (IR-radiance detection) with a maximum sensitivity toward short light wavelength (blue ~ 460–480 nm). Melanopsin works directly with the Vitamin A cycle (retinol) in the brain to allow neurons in the non visual imaging pathways to create a timing mechanism to tell about the photoperiod of the environment. This is one of the cornerstones of how the “eye clock” forms the gears of time within the human brain. Vitamin A coupled cycling in the brain helps set the molecular clocks to fine tune the timing mechanisms of the light induced circadian rhythms. When blue light from AM sunshine first enters our eyes, vitamin A within the brain parenchyma transmutes the light into a chemical signal that signals it is daytime. This signal is yoked to the illumination opsin that uses UVA light in the cornea and the skin to decipher what time of the day it is because UVA light varies as the day progresses. When the neuropsin signal wanes with the Vitamin A signal, the clock timing mechanism in the central retinal pathways “observes” that dusk is approaching. It is at this time sensory acuity in the melanopsin receptors is heightened by dimming light. Vitamin A is also known as retinol in the literature.
People have forgotten that a deficiency of Vitamin A leads to night blindness and to poor autophagy in cells. This means when Vitamin A is low, mitochondria in the eye swell, and heteroplasmy rates will be higher. This is the reason why all astronauts develop optic nerve swelling when they spend too much time in space disconnected from the sun and grounding to the Earth. Interestingly, autophagic induction by retinoic acid has been shown to be critical for both the removal of the toxic proteins in diseases like breast cancer, leukemia, and progeria. Retinol has also been shown to be an important co-factor in T cell activation in our immune system. Autophagy is essential for and upregulated on T cell activation and AMPK activation. AMPK is activated by both exercise, fasting and metformin, but requires leptin sensitivity with respect to light in the eye from your environment first. Proof of this concept is tied to the fact that 1,25 Vitamin D3 has been shown to activate AMPK in vivo to help recycle protons in 3 key metabolic pathways to improve the charge on the surfaces of cells and inside the cytolic water made by mitochondria. Changes in the retina are a sure sign that heteroplasmy rates are rising and it is one of the key things clinicians and patients need to monitor in the coming 5 G world that will be using TetraHertz RF frequencies in communications. This will massively effect the way cells charge themselves, it will effect protons spin, size, and composition in all tissues. Both pathways are required to be activated to significantly increase mitochondrial biogenesis and to recycle protons at the SN-2 postion of the glycerol back bone and the 2′ carbon in sugars. They also determine what type or protons are incorporated into the 3′ and 5′ carbons in ribose used in DNA and RNA. These things have far reaching implications for humans in altered environments. Increased AMPK activates ULK1 to induce autophagy, and promotes activation the master antioxidant transcription factor Nrf2 pathways. This explains how Vitamin dys-regulation of A and sulfated D3 can cause circadian diseases by destroying the ability to induce autophagy at sleep. It also explains why triglyceride levels rise and with cholesterol levels in people in bad environments loaded with nnEMF frequencies.
Vitamin A plays a role in night vision in rods. This tells us why Vitamin A and melanopsin are coupled thermodynamically in quantized fashion. Rod opsins are called rhodopsin. We have red, blue, and green rhodopsins in the retina. All opsins have an isoforms of the vitamin A molecule covalently bonded to proteins in the opsin. Retina’s with lowered Vitamin A levels have shown us they lead to sleep disorders which directly impact cellular regeneration under the power of melatonin. When melatonin levels are low so is tissue sulfation and heteroplasmy rates also rise. In fact, for every increase of 18 ug/dL in vitamin A/retinol levels has been correlated with a 22% lower risk of sleep disorders in NHANES data.
Lutein and zeaxanthin are non-retinol carotenoids found in seafood and eggs that accumulate in the retina to protect against the eye from photic damage from an altered spectrum of light the eye senses. This is part of the reason why the Epi-paleo Rx is built around reconstructing the fiberoptics of the retina to help the brain decipher light signals well. As you heard in the Vermont 2017 talk I view the central retinal pathways as a giant semiconductive circuit that controls all growth and metabolism pathways in humans. The eye uses AM starlight to determine when darkness exists. That AM light is critical to recycling protons with a 1/2 spin in cells. A lack of AM light allows more protons with a +1 spin into our cells to cause havoc.
MOST OF YOU KNOW NEUROPSIN is found in the cornea and the skin. I predicted long ago soon many more opsins would be found in the subcuatneous fat mass because this is the only explanation that helps explain why hypothyroid diseases have explaoded in a blue lit world. It is also why I have told all my members that covering their skin at night in artificial blue light makes a lot of sense. Just because we did not have the proof that our major blue light opsin was present in our fat mass does not mean it is not there. The explosion of hypothyroidism is unexplained by any bio-chemical mechanism. The bio-physics explanation is easy. Look at the picture below and see that blue light (labeled violet below) penetrates directly to the fat mass.
Melanopsin is the blue light photo-receptor (435-465 nm target) in our eyes responsible for relaying sunlight to the SCN to entrain the central pacemaker via the central retinal pathways. In my Vermont 2017 talk I made a prediction in the Q & A that we would soon find that melanopsin would be present in the human fat mass to explain why hypothyroidism and leptin resistance occured in the fat mass under the power of night time blue light exposure of the skin to cause mitochondrial damage. A group of scientists accidentally discovered melanopsin in our subcutaneous white fat cells: HYPERLINK
Now we have proof that my predictions that melanopsin would be found in white fat was spot on. How do these things link back to the central story of obesity that begins in the brain at the leptin receptor in the central retinal pathways? Light on the eye and the skin are the key non linear stimulus to obesity. This is why I have always said obesity is an inflammatory condition of the brain. People have forgotten that the brain and skin are both derived from the same tissues in the embryo, namely the ectoderm. Light is what links them both. Scientists should have expected photo-activation of melanopsin by the absence of blue light from the sun at night. Why? Absence of blue light at night reduces the size of lipid droplets and lowers leptin levels in the blood for the 4 hours of darkness before midnight when leptin signals enter the hypothalamus that I spoke about 8 years ago in the leptin series of blogs on my website. Interestingly, if the bio-chemists really understood light, they would have realized immediately that lack of blue light at night should also be expected to reduce adiponectin. It turns out the recent report on melanopsin in mice fat mass does just that.
The specific details in quantum mechanics of light is why Lady Evolution built the human retina as she did. If you look at its anatomy you will see it appears like the retina is built backwards. Once you understand why she did it, you’d see why I made the prediction that malanopsin and neurospin would both be found in the skin and subcutaneous fat mass of mammals. In fact, in some papers from 1990’s it was shown that the illumination of a simple penlight on theback of a humans’ knee was the only stimulus that was needed to turn off melatonin function in humans. Nobody could explain the effect back then, but I mentioned in long ago in blogs and webinars and told people the reason it could happen was because of blue light exposure from the penlight had to effect the opsin system. Absense of evidence is not absense of effect. With respect to the retina, it only appears it was created backwards when you have a cursory understanding of anatomy, a lack of knowledge of how energy trumps anatomy in cells. Moreover, it highlights how light acts as the ultimate non linear stimulus to bio-chemical pathways. It shows us how scientists today do not have a quantum understanding of the non linear aspects of light it uses to make sense of our world using small changes in charges of electrons and protons by frequencies of light. This is the key to becoming a mitochondriac. Blue light must be COMPLETELY subtracted from our lives because of how the opsin system is built by nature. I mentioned this in Mexico to Julia, one of my 19 year old members when she came to dinner scantily dresses when she ask me why her mypoia was not improving. If you protect you eyes alone by blue light and not your skin, you have built a half truth in your life. Begin to cover most of your skin at night, and especially the skin around your thyroid gland.
It takes the non linear aspects of light to build what appear to be a counterintuitive retina. Control of photo oxidation in the retina is maintained by the carotenoids (flavins) from a marine diet. Those carotenoids are key to controling precisely the movement of protons in mitochondria and in the retina’s network of bio-molecules. Both of these unusual antioxidants are contained in them. Eggs can be used as a bridge when seafood is sparse, because eggs of mammals also concentrate these chemicals to help control protons recycling in mitochondria. This is why all mammals are drawn to eating eggs of other mammals in nature. Lutein and zeaxanthin improve the ability of the human retina to preserve vitamin A from degradation of light using the GTP type A rhodopsin receptors. Lutein and zeaxanthin, like DHA, are selectively taken up into the macula of the eye by the exosomes of RNA when photodamage occurs. In this way, light damage in the eye strenghtens the eye because it improves the redox potential of the eye, by destroying the normal anatomy to increase the recycling of protons in the retina, where they protect against age-related macular degeneration by protecting us from the blue light hazard at night. The November 2017 webinar laid out this mechanism in detail. In the very same webinar I mentioned that humans stored their stem cells in their subcutaneous fat for use later when the environment became more favorable. This blog now sheds more wisdom on why the subcutaneous fat mass has our most valuable cell present in it. Might it be because we have our blue light opsin system also present in this tissue? Might it be that melanopsin in our fat is waiting for a “specific light signal” to be present before we can use our stem cells to regenerate our tissues?
The answer to these questions are: YES.
Recall that blue light photo-oxidation lowers DHA content of the retina and central retinal pathways. It also lowers the charge and this slows protons recycling ability in cells of the eye. Myopia and retinal thickening results from this effect. This effects the anterior visual pathways ability to work as bi-directional semiconductive gate for information control from the environment to the brain where the leptin receptor is located. Darkness is needed to convert serotonin to melatonin in the gut; then and only then can melatonin travel to the pineal gland to work on the sleep mechanisms there. The melatonin travels via the blood plasma, and the melatonin in blood effects the mitochondria in WBC’s, platelets, and in the pineal gland to get us the “quantum alter” of REM sleep were cells regenerate using autophagy and apoptosis programs in mitochondria. These sleep cycles are massively improtant in clearing deuterium from the system at night. Melatonin lowers heteroplasmy rate because it enhances proton recycling at night (subtracting deuterium from our blood and CSF) to improve the charge of tissues and facilitate regeneration by lowering heteroplasmy in mtDNA. The absence of blue light at night is THE critical non linear light effect for melatonin to operate when the sun is absent by lowering temperature. When temperatures are lowered it lowers the strength of the kinetic isotope effect of deuterium. The lack of blue light at night via the eye and skin is needed to catalyze the solid state conversion of serotonin to melatonin in the gut and blood by using the process of methylation in cells. Methylation is the key epigenetic program that controls regeneration and mitochondrial heteroplasmy. Methylation during darkness mediates circadian clock plasticity in peripheral tissues. Methyl groups have three hydrogen bound to carbon. If these hydrogens are deuterium and they are bound to RNA and DNA epi-genetic expression of melatonin and the opsin systems are LOST. This is why astronauts who are identical twins can go in space and the one that comes back from space will have increased methylation and heavy deuteration of the RNA and DNA. One of our former members, knows one of these twins and I told her when Kelly went into to space I bet that he comes back with very specific eye changes and methylation defects due to an upregulation of this pathway. Now it turns out I was correct. Check out this hyperlink.
This solid state process in cells on the spin of electrons and protons requires a large EZ must be present (DDW creates the largest EZ and redox potential in a cell) and the presence of vitamin B12 and folate. B12 is made in the presence of daylight. Folate is destroyed by strong sunlight and this is why it works at night on DNA to effect methylation of our nucleic acids. Methylation is usually a stop code signal in DNA. I predicted that the space astronaut would return and his genome would be turned on, because all things with a bacteria heritage increases their volume in space to begin to grow because of how volume changes marry to the cell cycle in humans. These changes, if left to go on chronically lead to many mitochondrial diseases like cancer. Why?
Hypermethylation of human DNA is associated with silencing tumor suppression genes that can lead to oncogenesis. This should be really bad news for NASA and any astronaut that chooses to go to Mars. Could this be why human cancers on Earth are growing over the last 120 years? Is our use of the light spectrum in technology gear and screens the reason behind this change in signalling in cells? I think so. Kelly exhibited this change when he returned to Earth. Today, researchers know that DNA methylation occurs at the cytosine bases of eukaryotic DNA, which are converted to 5-methylcytosine by DNA methyltransferase (DNMT) enzymes. You should remember that all the DNA bases are made by the Pentose Phosphate Pathway along with their ribose sugars. I believe the key to understanding the epigenetic program is tied to the type of protons in the 3′ and 5′ carbons of the ribose of these cytosines. Methyl groups have 3 H+ protons. There amount of deuterons present in theses methyl groups would have large kinetic isotope effects on the bond strenght to nuclear bases. People forget deuterium adds a ton of mass to this equation and diminishes how much energy can be liberated from DNA. Moreover, the length of these methylated nuclear bases are markedly altered because of the kinetic isotope effect of deuterium. these radical differences in the nuclear magnetic moments of deuterons and H+. The altered cytosine residues are usually immediately adjacent to a guanine nucleotide, resulting in two methylated cytosine residues sitting diagonally to each other on opposing DNA strands. This diagonal relationship is a geometric arrangement that would affect what light waves in the electromagnetic spectrum to alter their activity. People forget that light waves have their electric and magnetic field at 90 degree angles to one another and this diagonal arrangment is ideal for light to interact with DNA/RNA.
The protons physical state, I believe, is the key to decoding the epigenetic programs of life. Different members of the DNMT family of enzymes act either as de novo DNMT’s, putting the initial pattern of methyl groups in place on a DNA sequence, or as maintenance DNMTs, copying the methylation from an existing DNA strand to its new partner after replication. Methylation can be observed by staining cells with an immunofluorescently labeled antibody for 5-methylcytosine, but we have no way of knowing if the hydrogens on methyl groups are dueterated or not. We do know that deuterium depleted water improves survival in all cancers so far tested in humans. In mammals, methylation is found sparsely but globally, distributed in definite CpG sequences throughout the entire genome, with the exception of CpG islands, or certain stretches (approximately 1 kilobase in length) where high CpG contents are found. The methylation of these sequences can lead to inappropriate gene silencing, such as the silencing of tumor suppressor genes in cancer cells.
Currently, the mechanism by which de novo DNMT enzymes are directed to the sites that they are meant to silence is not well understood. I mentioned this in the January 2018 webinar and in the 12/17/2017 Q &A on genetic diseases. I believe they are 100% tied to the physical state of the proton and I think the proton spin process is critical in the understanding. I no longer think genetic mutations are needed to understand how DNA signaling can be altered by simple deuterium replacement on the DNA backbone.
For all of the reasons I stated above, I mentioned to my members long ago that going to Mars for NASA was not a tenable plan based upon what we already know about mitochondria, light, and proton spin. I believe the key data for us to know about astronaut Kelly return from space was to see if he had the tell tale signs of methyaltion defects present or not. Kelly himself released his data and now we know it is true. Havng Kelly’s data would help a quantum clinician decipher the epigenetic toolbox code further. My bet he comes down with a mitochondrial disease before his twin, who stayed on Earth does, and I bet it will happen in the tissue where his methyaltion defects are elevated. These tissues will have higher heteroplasmy rates and lead to diseases. This is why you always hear me tell you the best situation for humans is to be in environments that keep our mt DNA quiet to keep our nuclear genome silent to improve our energy and charge flux of electrons and protons in mitochondria.
These are the two chemical arms in cells that tell the quantum clinician if a patient is solar deficient and/or blue light toxic. B12 and sulfated Vitamin D3 are linked to the presence of AM sunlight frequencies and this is why pernicious anemia is associated with a lack of sun. This type of anemia results in premature RBC’s being released into the blood and the cells are larger. We know that hypermethylation leads to defects in stem cell differentiation in biology. The stem cells are hidden in bone marrow and our fat mass. Blue and red light get to these tissues easily as the picture below shows.
This link of B12 and folate was another link found by Fritz Hollowich in the 1940’s and I covered this link in my Vermont 2017 talk. He confirmed this finding, first reported in the literature in 1927.
Recall that melatonin optimizes mitochondrial DNA to control heteroplasmy rates to maximize energy generation in tissues, while also optimizing tissue level sulfation too because of the effect of charge. Charge is mostly related to the type of protons we have in our tissues. The less charge we have the less sulfation we see in tissues. Light stimulates the non imaging portions of the anterior visual system are designed to create a non linear trail of photoelectric changes in proteins that amplify the incident photon signal the retina senses by using protons size, shape, spin, and charge to facilitate the amplification.
HOW SO?
Melatonin is also an antagonist of the aromatase enzyme so it lowers estrogen in tissues. I showed this in my Vermont 2017 video on youtube. Plasma Vitamin D3 levels happens to be a “light stress hormone” that builds melatonin levels in the RPE of the eye and locally where full spectrum light penetrates our cells. Diseases in men and women with high estradiol (E2) levels in men are signs of sunlight deficiency and a low quantum yield environment because of increased methylation defects related to poor proton recycling. Poor AM sunlight exposure also causes a pro-estrogen pro-growth state. Left untreated, this will cause an increase in the % heteroplasmy rate to cause insulin resistance to manifest in cells because of the “proton crisis” in tissues that lead to many downstream effects in the hormone panel, tissue charge, and the lack of proton recycling. This causes glucose to rise in the blood plasma, we lose control of sulfation of the proteins in our skin and blood plasma, and eventually metabolic syndrome can manifest when the liver is afflicted by too many deuterons. The liver is the source of most of the gluconeogenesis in the body. Dr. Wallace talks about it in the last cite below. He also mentions it in this video too.
The human liver is a lot like the sun (vidoe has it close to the 24-26 min mark). It is where most hydrogen energy occurs in the body and it controls most proton recyling in the entire body. It has a massive effect in the gut and when deuterons are more numerous in the gut lining the gut loses its charge and this is why it become permeable. The only way to repair it is to increase the redox potential of the cell to get rid of deuterons for H+ in the entire system.
When these quantum changes begin to all manifest at cytochrome 1 (NADH) we begin to observe changes in lipid oxidation, lipo-protein changes which result in higher mass and inertia in the blood. This increases the viscosity of the blood and lowers the exclusion zone in blood plasma. ECT slows because the matrix become overwhelmed with too many deuterons over H+ and it swells and the charge on membranes drops quickly. This acts to further decrease the recycling of protons. The “smart natural answer” is not blood pressure medicine, statins, and glucophage, in this case. A better answer is to follow nature cues and get that person in the sunlight eating animal fats and drinking deuterium depleted fluids of any kind. Sensible sun exposure with connection to Earth is best able to charge separate water, charge cells, control proton recycling to build an optimized photoelectric battery around every protein in every cell in the body to allow for proper function to lower ubiquitin marking and control cell and mitochondrial swelling. If the battery function around the protein (water from mitochondria) is not well maintained the protein will be selected for replacement at a huge energy cost to the cell. This is stimulated by the loss of charge and the resultant swelling. The sun’s photons allows cells to make melatonin initially in the globe and its presence there is then amplified throughout the central retinal pathways to the frontal lobes. These photochemical interactions generalizes via statistical mechanics to elevate the production of melatonin and dopamine throughout the visual systems and into the brain. Serotonin is the braking mechanism for melatonin, and glutamine is the braking mechanism for dopamine release.
This is why glucose and glutamine metabolism are up-regulated in a Warburg shift in mitochondria. It is not a pathologic problem. It is a the mitochondria’s reaction to get rid of deuterium and replace it with H+ and change the ratio in all tissues as fast as possible. The H+ in NADH must be deuterium free to work its magic at cytochrome 1 to make the correct free radical signal. This H+ must come from the water in the matrix. The breaking mechanism is wholly tied to the effectivness of recycling protons in cells to eliminate the ones that have a 1/2(e) charge (H+). The protons favored by all living things is H+ that carries a +1(e) charge.
Our eye clock, fat mass, and our camera vision, and all of our other senses like touch, smell, taste, and sound— rely on very specific atomic interactions, which rely in turn on the interactions of electrically charged particles. Light is what alters the charge on electrons and protons in all living systems. The light life works with is solar light and not man made light. Man made light frequencies alters the charge that mitochondria expect during the day night cycle. Light can alter the electromagnetic interactions in all these sensory systems to tune its crystalline lattice or ruin its optimal melody, we call life. Even touch sensation, though for more subtle reasons, relies on electromagnetic vibrations and interactions. Since human senses are all based in electromagnetic interactions of some sort, they are all directly affected by photoelectric interactions that begin in the smallest semiconductors of eye and skin cells. Light first touches melanopsin in the eye and our fat mass begin to build time perception in living things.
This occurs because melanopsin ipRGC have a low spatial resolution and long latencies as compared to cone and rod responses, and they show the ability to integrate photic energy over long periods of time. This firing pattern has to marry to the optical coding of the skin from the opsin system as well. When it is not, the circadian mechanism for deuterium clearance is altered and will not be OPTIMIZED.
IS MELANOPSIN LINKED TO DEUTERIUM CLEARANCE BY FALLING BLUE LIGHT EXPOSURES IN THE EYE AND SKIN?
When light dims as the day ends, melanopsin is activated in all eutherian mammals in their tissues derived from ectoderm. Eutherian mammals are the animals who survived the KT asteroid event you heard about in the last chapter of my book. In non-mammalian vertebrates, they have an intrinsically photosensitive iris in their eye and skins resulting in a local pupillary light reflex (PLR) and skin color changes to sunlight.
Melanopsin is a relatively new photopigment found in the eutherian mammal and human retina and subcutaneous fat mass which regulates non-visual functions of light such as the synchronization of the sleep-wake cycle, and relays photoelectric and magnetic signals to the pineal gland and the allows the pupillary reflex to work in dim lighting for mammals to see as the sun rises or falls. It also appears it is the key quantum event that links to the sleep cycles that begin the clearance of deuterium from CSF and the blood plasma during the various sleep cycles in these animals. If the system gets mixed messaging, it appears to effect the clearance of deuterium from our tissues that lead to an inability to regenerate properly when the sun light absent.
This “type of time” built in the hydrated proteins of the retina and subcutaneous fat is critical in the shape shifting cascade that occurs in this light system. The critical difference in this type of time is how we are able to observe the “past” and “future” time in reality. The idea of “past” and “future” only exists in human reality if heat is present somewhere in the cascade of energy transduction. Thermodynamics is the science that teaches us this and this science was innovated by Ludwig Boltzman. He developed statistical mechanics, which explains and predicts how the properties of atoms, such as mass, charge, and physical structure change with time. These things determine the physical properties of matter in the retina once light hits the photoreceptors and water. When this collision occurs, things like viscosity, thermal conductivity, and diffusion change and build the reality we all enjoy. Heat is a red frequency of light and it makes atoms and molecules move in certain ways. Heat moves dueterons and H+ differently. Heat concentrates deuterons and H+ moves away from heat sources and goes to the surface. This was critical at life’s beginning and it is the reason why I am not a fan of hot coffee or tea.
Warmer temperatures concentrates deuterons, fluoride, and bromine. All have massive effects on H+ in water and lower the amount of DDW in the matrix and lower the size of the EZ. When the size of the EZ is lowered the redox potential of the cell SHRINKS.
Heat is liberated in the mitochondria of every mammal on this planet.Heat creates reality because it creates TIME by moving things with mass. Protons have a lot more mass than electrons, therefore red light (heat) is optimized to work with proton motions and recycling programs in cells and mitochondria. This maybe hard for you to accept initially, but when an Alaskan native sees spring break from the winter for the first time, they always remark that the pace of life seems to pick up in spring and accelerates in summer. This is not just a perception, it is reality related to the changing diurnal aspects of light in that season at that high latitude. Light is constantly present 24/7 at this time.
The reason is simple and linked to physics of light. At polar regions sunlight is compressed in to shorter periods of time in spring and summer, so you can see the effect of powerful light on time in living systems very easily. Spring is when heat and light return and life speeds up because time speeds up because proton recyling improves tissue wide. Heat comes to us in a form of red light from the sun. That light comes from H+ in the photosphere of the sun. 42% of sunlight that falls to Earth is IR-A light that looks to control the movements of light hydrogen. UV light is also capable of generating heat because it can be shifted to red photons in a hot plasma (like the EZ) to make more heat, but only 1-4% of sunlight is in the UVA/B ranges that falls to Earth. This frequency shifting of light is what the Q- cycle and water does in our mitochondria to build a strong EZ around it. The directions of these motions caused by red light in our mitochondria are critical to understanding probability of quantum mechanics of protons in cells and to really understanding the reality of time creation by living things. Quantum mechanics is the science of probability.
In the 21st century statistical mechanics of heat movement has now been extended to electromagnetic and quantum phenomena by QED theory. This was important in me figuring out what Szent Gyorgi really found when he noted that fumarate hydratase controls water creation in mitochondria. This enzyme is critical in the placement of H+ in TCA intermdiates, in glucose, and in glycerol, and glycogen back bones. I realized the rules of QED would control all aspects of protons. Light can control the charge, spin, radius, size, and movements under red light because Feyman extended the thermodynamics of Boltzman. Today, because of Boltzman’s work, we know both space and time must vibrate (if Einstein is right about them) or move, but we still do not know how to describe this process well with words or with mathematics. Einstein tried to do this and came up with a geometric solution of the idea of curved space/time. The Standard Model of physics has embraced this idea of curved space/time as gospel 100%. I told you in the Sun blog in the reality series , I have rejected this idea because of how I view time creation occuring via light transmutation to other forms of energy. Humans only see energy when it is transformed from one form of energy to another. This is because of the Quantum Zeno effect. Once the living system observes the effect, the effect vanishes from reality by quantum laws. This offends common sense, but it is how nature operates.
Think about lightening in a storm. Its power comes from the solar wind, and it is created when this light is slowed by the ionsophere, and captured and transformed into lightening by water droplets in the sky, that then discharges the energy in light form we call lightening. This is a big deal because the bolts that hits Earth and unleashes the nitrogen cycle for plants and animals to make foods from photosynthesis to build the chloroplast nitrogen cage and breaks the triple bonds of N2 to make N available to plants. This process is the basis of the entire photosynthetic pathways that form the food webs on Earth. That makes it pretty important. The threads that nature uses sunlight for are vast and hidden from our perceptions in our senses because of the rules of quantum mechanics. The one sensor that always pays attention to them ALL is our mitochondria. It reacts to energy drops by altering its charge to swell and change cell volumes. This is how quantum mechanics is transformed from the QED rules of light and charge to Boltzman’s three thermodynamic laws.
Mitochondria, like the sun, also release heat. Heat, as we all know from our observations in reality, always moves from hot things to cold things. This should make you ask yourself, why does heat always seem to go from hot to cold and not vice versa? Is there a universal law that says this is axiomatic? It turns out there is no universal law that tells us this. So this raises the question why does it always appear this way in our reality that HEAT flow goes from hot to cold?
IS SHAPE SHIFTING JUST ANOTHER DESCRIPTION FOR THERMODYNAMICS?
Light from the sun has energy that “shape shifts” Vitamin A, the opsins, and the protons in the eye and skin to alter their charges, and that small charge alteration is capable of confirmational changes in the rhodopsin system (GTP circadian gene sets). These small changes are also what destroys melatonin’s ablity to control mitochondrial DNA in cells. These changes alter the thermodynamic ledge in the retina of the eye and the central retinal pathways that lead to cascading effects from the cell membrane down to the mitochondria to drive energy flux through out the retina to the central retinal pathway. Vitamin A is tightly bound to opsins in nocturnal mammals like rodents (mice in the melanopsin cite below), but it is loosely bound in diurnal mammals like humans. The loose binding is why humans are so sensitive to blue light photo-damage at night. If deuterium is in this system its kinetic isotope effects massively influences the bonding affinity to ruin how the system operates with light!!!!!
These small changes in these proteins alters the tension within the cell water (where protons are excluded to move and recycle) and this changes the charge around all proteins and lipids, and carbohydrates involved in metabolic pathways. How protons move in these pathways was first worked out by Albert Szent Gyorgi in the 1930’s. This effects the proton motions and the potential battery effect in cell water around every protein in our cell when this change occurs. This cascade then immediately effects the output of energy flow in mitochondria by small changes in volume in the outer mitochondrial membrane space which changes the charge in the outer mitochondrial membrane which connect directly to the endoplasmic reticulum membrane (ER) of the mitocondria in the retina, fat and skin. The ER is the site of protein construction in the cell. The ER is connected directly to the Golgi apparatus that does post transaltion modification of the protein to add lipids, carbohydrates, and protons in specific regions of the completed translation before the cell deploys this bio-molecule. Where those protons are deployed, determine how sensitive the entire cell, tissue, and organism is to light radiations in their environment. This is how one becomes electrosensitive, in my view. When more protons are 1/2(e) charge (deuterons) versus H+, the more sensitive one becomes to all aspects of the electromagnetic spectrum and the more heteroplasmy rates rise with an associative increase in ubiquitination rates.
The Endoplasmic Reticulum is physically, electrically, and optically connected to the outer mitochondrial membrane which vibrates and sends its shockwaves through the cell water to the inner mitochondrial membrane where the cytochrome proteins change energy from one form to another. Here the mitochondria make water, H+, and ATP.
In proton chemiosmosis, the energy stored in the gradient is used to make ATP. Because protons are electrically charged particles (+1(e), the potential energy stored in the proton gradient is electric as well as chemical in nature. The electric component corresponds to the voltage difference across the inner mitochondrial membrane, with the matrix of the mitochondrion negative and the intermembrane space positive. The membrane is critical in protons recycling because the charge acts to filter out all the deuterons and favor all the H+ for recycling in the matrix and in all our bio-molecules. This charge differential in the mitochondria sets up a huge capacitor that is surrounded by another water capacitor filled with a large exclusion zone driven by the heat release of the proton gradient and electric field. It also is the major sieve that filters protons in cells. This is how the two sides of the energy equation remain so efficient in eukaryotic mitochondria. The last part of the equation is to understand why ATP breakdown to inorganic P and ADP, AMP, and adenosine are important in mitochondrion. It also begins to explain why we have two separate adenine nucleotide transporters (ANT1 and ANT2) in our mitochondrion as well.
Watch this video again to pay attention to the ANT1 and ANT 2 importance in heteroplasmy development. You’ll begin to see how deuterium content affects things like sleep and regeneration to lead to many mitochondrial diseases.
2018 Mexico members teaching point made over and over again at the beach between myself and an industry insider: Make friends who have tattoo’s when you city goes 5G because they will be the best indicator of when you will need to migrate because of the electric fields that will generate at their skin. However, I would not go with them to fill the car up with gas at any gas station given how much charge their skin will hold and carry and how this energy will have the ability to jump conduct to their metal car. Static electric energy will be a massive 5 G problem beginning this year. Ask anyone who has been in a smart meter fire or anyone in the Southern California fires. Both of these scenario’s are linked to this hack as I described to my members on the beach in Mexico this week.
What is the best 5G tracker I know right now based upon the bio-physics? I pay attention to my patients and friends with tattoo’s. The more ink they have the better indicator they will be when you environment is turned to shit by cell carriers. I had an INDUSTRY INSIDER on the beach to back up my claims for my members too. Membership matters folks!!!!! This is why I draw them to the sun and to the crater. They become wiser to nature’s rules and less subject to pill pushers.
If they have lots of red ink I am more interested in monitoring their lives because of what I’ll learn. When they start coming in with lots of complaints tied to mitochondrial energy loss I know its time to go recheck the local environment. The excess energy in the skin will lead to more deuterium collection in the mitochondria below the tatoo leading to more dysfunction making them a NET deuterium collector further ruining their mitochondrial function. PREDICTION ONE 2018 made in Mexico this week on the beach with an INDUSTRY INSIDER PRESENT.
Tattoo INK = transition metals = heavy metals = geo-engineering of the atmosphere. Transition metals found anywhere (vaccine, road tar, highways, and medications) have D shell electrons. These D shell electrons draw nnEMF to them, especially RF and microwaves. RF tends to affect surfaces in a big way so the surface skin and RF is a huge issue with tattoo’s. RF generates massive electric fields surfaces. This hass massive implications as all my members heard from an INDUSTRY INSIDER this week during our member retreat.
When 5 G hits I am expecting tons of people with tattoo’s come in which mitochondrial ailments that will stump their physicians. What did I say about heavy metals in Ubiquitination 4 blog post? It causes massive local circadian disruption because it speeds the local molecular clocks in front of every gene in that cell faster than the main clock in the SCN of the eye. This is effectively what eczema is on the skin. It is also why sunlight help eczema and why RF/microwaves, and blue light make it worse. Normally in a good brain, cortisol shows up in early morning when solar blue light and red light are balanced and UVA and UVB are absent. This release helps germinate new neuron circuits during daytime, but melatonin is critical in pruning arborization in neurons and new neuronal connections and proteins. Melatonin is made by the combination of IRA and UVA. So if the tattoo blocks this you just created a circadian mismatch. It is very active in ubiquination in the brain and the skin. Why? Both brain and skin come from neuro-ectoderm in an embryos’ layers. People forget that. This is why Vitamin A and D3 exist. They are chemicals that allow these two organs to speak to each other using light frequencies they sense. When the light cannot get in properly, diurnally, or in circadian fashion skin and brain diseases from the mitochondria explode. That is what we see today. Melatonin has been widely studied in biology for its role in photoperiodism in seasonal breeders; but it is also a potent antioxidant. Its main effect is controlling mtDNA!!!! It controls heteroplasmy. Ubiquitin, a protein also widespread in living cells, contributes to many cellular events, although the most well known is that of tagging proteins for destruction by the proteasome. Melatonin interacts with the ubiquitin–proteasome system to regulate the central activity of thyroid hormone type 2 deiodinase; the subsequent regulation of T3, is central to the melatonin-induced changes in seasonal reproduction and seasonal changes in metabolism. This is how light changes the surfaces of most animals including humans when the sunlight changes. Today man rarely is in sunlight due to his teether to technology which brings them inside the power grid (jump conduction MORE LIKELY and unhackable) or in front of a blue lit mobile. This is also why excessive man made blue light can alter thyroid function in humans. People with tattoo’s also hurt themselves because they limit how much UV sunlight can get into their skin and deeper layers where the blood vessels have RBC waiting to be irradiated as UVA light releases NO to get the job done. Did you know that UV light on the skin is how keritinocytes get rid of deuterium from the blood plasma normally? Yep………..that is the other part of how the solar callus works to deplete us of deuterium. You should have come to Mexico folks. You missed a ton of new info and deeper discussion or deuterium on the beach this week.
This is why most people with tattoos I am confident in calling low dopamine and high deuterium humans because of the alien fields their skin generates. They just fail to realize why I say as I do. Now I am stepping on the gas pedal to warn you of what is coming. Physicians better pay attention to these risks. If they don’t they will be flumoxxed why so many young people with tattoo’s are coming to see them them conditions they cannot explain. The etiology will be their CELL PHONE’s 5G network. Low melatonin always walks hand and hand with low local and systemic melatonin levels because both are solar hormones made by UVA and IR-A light combination found in the AM and later PM. Many papers have shown that glutathiolation (sulfates from cysteine think EE 12) of this enzyme protects proteins from unnecessary degradation by ubiquination. So the sulfur is normally carried by melatonin, may limit protein degradation in the brain. So if the melatonin is not present nothing get sulfated by sun exposure. If they take ANY Melatonin supplement the effect will be MAGNIFIED and not helped. I bet your “bulletprooff” executive pill sellers won’t tell you that. My members were warned this week of what it all means and why it is all connected.
What are the five main things sunlight sulfates? Cholesterol, heparin, platelets, DHEA, and Vitamin D3. This begins to tell you why tattoos and low dopamine are strongly correlated because of increase of deuterium fractionation.
When this process is broken, the result is low brain sulfate levels, while excessive amounts of metals precipitate out in our tissues. So when the functional medicine doc says you have heavy metal toxicity it means to a mitochondriac that you have a DEFICIT of sunlight and a net ability to assimilate EVEN MORE DEUTERIUM in you matrix for some reason and not a heavy metal issue. When you realize that deuterium is the heavy metal version of H+ for the matrix you begin to see a huge problem developing. That is how a half truth leads you to a wallet biopsy for a chelation treatment. I highly do not recommend this because I am a person who understands how the quantized process works in the skin. Tattoo’s make this worse and lower the dopamine and melatonin levels innocuously as one ages. Precipitation of metals in tissues have the atomic effect of speeding up our organ clocks because we are adding atomic mass to the mitochondria in the tissues feeding sensory input via electromagnetic radiations in relation to the SCN. This ages you faster using the theory of relativity. This is why NASA will have to use DDW to get people to MARS. See the cite below.
This assimilation of atomic mass from deuterium completely ruins the circadian mechanism signaling in the central retinal pathways by ruining the mass equivalence equation by reducing E 9energy) while simultaneously, increasing mass (“m” in E=mc^2). As a result of this small effect (non linear) this speeds up ubiquination rates and increases epigenetic activation because you are lacking solar light to run that software program in your cells. This implies all mitochondrial disease, like cancer, maybe simply due to excessive man made light perception and the deuterium collection phenomena and/or loss of solar light assimilation for some reason to cause a lack of proper epigenetic control. This usually activates the p53 genome that opens Pandora’s box to hell. Enjoy all those technology gadgets you got from the holidays. You might need a term insurance policy with their use.
How much do you know about hydrogen? I know I have taught you a lot about here recently, but do you think you’ve tied it all together to really understand how it all links to sunlight?
Bright light always induces stress and swelling and that small swelling stress stimulus is needed for life to awaken but the dose makes the toxin with respect to blue light. Blue light induces this stimulus by allowing more deuterium into the tissue irradiated with it to create some molecular crowding to stimulate growth. The red light limits the molecular swelling if it is present to control swelling and create regeneration by lowering the amount of deuterium within the cytosol and matrix. AM light provides this stimulus to awaken us and then red light regenerates the thickening of the retinal tissues so there is no excessive growth generated in the central retinal pathways, hypothalamus, the leptin receptor, and eventually the subcutaneous fat mass. Full spectrum sunlight contains the antidote of blue light just as seafood contains the antidote for heavy metals by having high levels of selenium to help improve the semiconductive electric currents in the lipid rafts of cell membranes. The AM blue light is designed by nature to create a quantized amount of swelling to stresses the anterior pituitary to make adrenalin, noradrenalin, cortisol, alpha MSH, beta endorphin, TSH, estrogen, and prolactin. UVA light is the light stimulus that turns off the optical deuterium switch to limit molecular crowding and curb the pro-growth stance of blue light. When you use fake light with a blue color temp of technology of 5700K, the light stress provides a chronic pro growth stimulus that never can be moderated because technology contains no UV or IR light to blanche the effects of blue light on deuterium. In this way deuterium is an optical switch that promotes growth. When it loses its solar light controls it becomes what causes the Warburg shift in oncogenesis.
Deuterium has a different magnetic moment than a proton. The ATPase is the magnet they work with. The magnetic moment of a magnet is a quantity that determines the torque it will experience in an external magnetic field. The Earth provides that external field. Deuterium has a large increase to its magnetic moment because of the addition neutron to the proton. The ATPase is a nano electromechanical torque magnet that exclusive works with the light hydrogen proton in the ATPase.
The ATPase is 100% quantum mechanical efficient torque engine with red light (600-3100nm). The measured magnetic moment and QED theory taken together, yield the most precise measured value of the fine structure constant in nature. Electrons are the mustang’s of life. They are constantly are mobile when life is present. Protons are corralled horses controlled by the sun. We obtain the action of life when we multiply energy by time. They are the actors of life whereas the relatively static proteins are the stage the drama of life begins. Life needed a conductor and quantum mechanics provided star light as that conductor that make proteins electronic conductors who use proton recycling to power complex nano machines in cells. The movement of electrons is key to life because it powers proton recycling and deuterium depleted matrix water makes proteins become carbon based semiconductors. Without deuterium depleted matrix water proteins are insulators and the atoms become inanimate. Life is animated. There are many ways of knocking electrons out of atoms. UV light is the most accessible to life. The simplest is to rub two surfaces together, but life chose to use sun light to do it for a specific reason. It is close to a free lunch as one could get on a planet being bombarded by light for 4.6 billion years by some version of sunlight. Sometimes we just fall into things that we don’t even seek to understand and nature uses it. These are the things that make life interesting. Electrons, in living things, are something I just fell into. And it caused me to understand how life used the asymmetries in protons in glycolysis, the PPP, and the TCA cycle to make water from sunlight to reverse photosynthesis and create the sea inside of every cell to make complex life possible.
Today, I am going to do just that. Watch the video above before proceeding.
Why won’t a biochemist ever solve cancer? (they subtract bio-physics from the equation of life and think this will explain it)
Light in the lab is not the same as sunlight. To get the answer you need to know this fact. So all studies on deuterium depletion effects and H+ fractionation must be done under sunlight to see the true effect in glycolysis, TCA, and the PPP. This is why metabolic ward studies will never equal what Weston A. Price observed in nature. It is why WAP and Schweitzer never saw cancer in the indigenious people they studied. They can never be equivalent. Is this why they never observed cancer? Is it why we are seeing cancer in modern man grow like mad? Yep.
Physics has proven millions of times in their experiments that the structure of mass determines the frequency it can resonate and this frequency dictates structure of plasmoid instabilities and the type of light that will work with it and what frequencies won’t. Biologists, specifically biochemists refuse to realize that this process is what drives biochemistry. Light from the sun has the ability to act in non linear fashion. what does non linear mean? It means a small stimulus leads to seismic changes. How can we disprove bio-chemists ideas right here in this thread? If you add one methyl group with it 3 hydrogens to the right cytosine of RNA or DNA it COMPLETELY CHANGES its bio-chemical and physiologic abilities. That is defines a non linear change. It is well past time we all realize this. Life is fundamentally bio-physical and not bio chemical because the manner in which bio chemistry works is when small things change, like the ratio of H+ to deuterium massive changes occur inside the TCA cycle.
This is why cancer occurs. It is a biophysical change inside the matirx which alters the pH and temperature of the water the matrix makes and this ruins the kinetics of the TCA to not allow it to function as cycle. It becomes a linear pathway and that pathway is what the Warburg shift describes to a T.
So I want to stop now an ask a question you have all heard before. Why does the Warburg shift favor glucose and glutamine when both bio-molecules are non essential to humans?
We can live perfectly fine without sugar and glutamine. In case you don’t know, glutamine is a non essential amino acid. Thus even if you eat none your body will produce what it needs from other sources. So it raises a really good question that bio-chemists, who have never figured out why the Warburg shift happens. Why does a broken TCA cycle want glucose and glutamine exclusively in a cancer state??
What is it about glutamine and glucose that is seemingly so critical in a cancer state?
This question of being “non essential” was critical in me asking the right questions of why young people were getting brain cancer in the early 2000’s at exponetial rates. Remaining curious is why it is critcal to understand why cancer cells make specific food sources essential when your mitochondria have high heteroplasmy rates. I found the answer was simple. In a cancer state we need a reliable vast new proton source that can be added into a broken metabolism to fix the problem of making DDW in the matrix.
So how did I figure all this out?
Let us tackle the glutamine issue first. Cancer needs glutamine to recycle TCA intermediates when the TCA cycle is filled with intermediates that are loaded with deuterium. This turns the cycle into a pathway. It can no longer operate as a cycle. When a cycle breaks it means allosteric and enzyme control is gone. This is why ROS and RNS signaling looks so biazarre in an cancer state. So the cell has to make glucose and glutamine 100% essential in those states where TCA intermediates have the wrong isotope in them. That is why glutamine and glucose metabolism is up-regulated in a Warburg shift. It also explains why AMPk pathways are raised in cancer, because it only goes up when ATP levels drop. They drop because too many protons are deuterated and this slows electron chain transport from NADH to oxygen. The result is simple, NAD+ drops, ATPase spin rates slow, the magnetic field of the ATPase slows and since oxygen is paramagentic is is no longer drawn to the ATPase. This causes a pseudohypoxia or hypoxic state. When hypoxia is chronic the cell has two choices. Default to the more ancient system of metabolism that used to control hydrogen flows in its H+ state under the power of photosynthesis. Glucose and glutamine.
Glutamine enters the TCA cycle before the fumerase step so it can repar and fix the TCA proximal intermediates via alpha keto glutarate step. Remember in this state, the cycle is no longer a cycle because of the kinetic isotope effect of deuterium on how it makes bond strengths between TCA intermediates 6-8 times stronger. This effects the way the enzyme kinetics are in a cell.
So if you’re staying with me you probably are beginning to see why glucose is up regulated too now aren’t you?
If you aren’t making the connection because you’re bad at science I will give you a boost. Glucose has 6 carbons and it is a ring. It becomes two 3 carbon linear molecules called pyruvate. Look above. See where it enters the matrix of the mitochondria? In the beginning. It can only get in if NAD+ is HIGH. Don’t forget this. That is cytochrome 1 of the inner mitochondrial membrane because a low NAD+ means a LOSS of membrane potential or redox inside the matrix. Now, what did I say about this in the Decemeber webinar of 2017? Yep………..you’re getting wise by being a Patron or member.
Now ask yourself this: Why does it take cells ten enzymatic steps to cleave 6 carbon sugar into two 3 carbon pyruvates when it appears way easier to do in a lab with a lot less steps? Then I asked yourself why does it take 9 enzymatic steps to remove two CO2 molecules in the TCA cycle? Ya’ think it has anything to do with the fact that the mitochondrial matrix reverses the photosynthetic reactions that take CO2 and H20 and make glucose? Take a look at this picture from my Vermont 2017 video on youtube. You think I had this all planned for to explain to all in step by step fashion? Yep.
So how does nature provide water for the photosynthetic web folks? How does rain form that falls on our head on Earth at different latitudes? Is the information in hydrogen movements somehow tied to the sun and water cycles in ways that bio-chemists are clueless about? Yep.
Now I want you to stop and watch the video below before proceding to blow your mind in explaining why the Warburg effect is seen in cancer states.
A cancer biochemist recently asked me at a conference, “what would cause the tumor to prefer glutamine over glucose if both can provide TCA intermediates? That’s something I have never been able to figure out.”
My answer was simple. I told him it was due to the heteroplasmy rate in the matrix and the simultaneous oxygen deficit in tissues.
He looked perplexed. He then followed up by asking, “I was wondering based upon your hypothesis why do only certain cells develop into a metastatic biomass? If deuterium accumulation is the problem how does it selectively create biomass? In other words, it seems as if this would become a systemic problem.”
I went on to explain that mitochondrial origins are bacterial, so when the broken matrix sustains enough deuterium damage, and cannot be taken out by mitophagy by a SO pulse at cytochrome 1, mitochondria regain ability to move from the cells in the cytoarchitecture of the tissue to find a new oxygen source and a new source of H+.
They become a damaged bacteria looking for a better environment. They look to leave and migrate from their current local environment in their host looking for a new terminal electron acceptor to survive and make energy.That is what metastasis is.
This is why in metastatic brain cancer, mets always go to grey white junction in the neocortex where the best mitochondrial density is located and where oxygen tension are huge because this is where blood eneters the brain. I reminded him about some basic anatomy of the brain. Arteries feed in from the subarachnoid space into the substance of the brain. So this means oxygen delivery in the brain is unique. Oxygenated blood enters brain via the surface. All cancers are hypoxic and look for new oxygen sources. Neovascularization is rare in the brain except in grade 4 gliomas which are deadly. Those glioma’s are called glioblastoma multiforman.
Every tissue has a variable metabolic rate and heteroplasmy rate. The brain has a massive metabolic rate and normally has to run on a low heteroplasmy rate. If heteroplasmy spikes for any reason neurologic function in that area will manifest. This is what headache, tinnitus, and myopia are all.
In brain cancer the second heteroplasmy spikes thermodynamics are no longer maintained. The brain can only tolerate a 4 minute insult. So when the brain’s TCA cycle is altered it is a big deal for physiologic function. This is why the brain’s mitochondria must control deuterium fractionation to maintain their super metabolic rates. Glutamine enters TCA before fumerase step so it helps repair the hydrogen source to the proximal intermediates of the TCA cycle via alpha keto glutarate. We must remember that deuterium has an massive increase in bonding strength so the TCA can no longer cycle or turn forward. Deuterium turns the cycle to linear biochemical pathway, so complex enzyme kinetics controlling hydrogen recycling are destroyed.
So neurons and glial cells need ways to get hydrogen substrate from glucose and glutamine because pyruvate cannot get in to them in the matrix as electrons on the electron chain transport system slows down. At this point his eyes got big. He realized immediately that just knowing bio-chemistry was not enough. You need to understand both bio-physics and the biochemistry to make sense of the Warburg shift.
WHAT ABOUT THE REACTIVE OXYGEN SPECIES IN CANCER?
ROS is a result of the cycle becoming a linear pathway and not a cycle. There is too much oxygen available and not enough hydrogen present to complete reactions. When too much oxygen is present and not enough hydrogen present ROS results. You get a lot of free radicals because the reactions kinetics are no longer controlled by sunlight and oxygen at each end of the redox chain.
When this happens amount of oxygen needed is no longer control by light frequencies at NADH. People forget NADH is a fluorophore protein that absorbs light at 340nm. This step is quantized by the sun. So ROS is not really pathonmemonic of cancer. It is proof that the matrix intermediates are dysfunctional. Just thinking reductively about ROS will never lead you to the right cause of the matrix dysfunction.
I want to remind you about what occurs in diabetes. What makes diabetes and cancer the same, yet different? Diabetics have no free radical superoxide (SO) burst. This burst is what stimulate mitochondrial apoptosis which can take out defective mitochondria. It occurs at cytochrome one where NAD+/NADH couple reside.
It is why most diabetics get fatter too, because their mitochondrial matrix cannot perform beta oxidation of their subcutaneous fat at night when they sleep. They tend to have mitochondria with pseudohypoxia and not frank hypoxia. The reason is simple. The amount of damage to the TCA hydrogen recycling determines how much oxygen is present or not in the matrix. Cancer is a hypoxic state and diabetes is a pseudohypoxic state. SO is a free radical that we need to get rid of bad mitochondria. Neither disease has enough of it. All free radicals have unpaired electrons. Cancer can or cannot have ROS or RNS depending upon oxygen supply to the tissue.
This explains why DM and CA are linked to a dynamic deuterium effect that can or cannot flow into cells. See deuterium is not always bad, it just appears to be this way when you do not understand how it works to make the metabolic rate of a tissue.
Diabetics have a lot of deuteration of the TCA cycle, but not enough to get to the cancer state. Small superoxide bursts lead to seismic changes in tissues. This defines a non linear effect. UV light is the only frequency from the sun that can participate in non linear effect and the NADH cannot be recycled when the TCA cycle is gunked up with deuterium. This is why NAD+ is always lowered in diabetes, aging, cancer, and any disease. This was found in David Sinclair’s paper in December of 2013. This is why ROS is all over place in different cancers. They all have variable defects of TCA dysfunction. Normally NADH light (340nm) is THE non linear stimulus in mitochondrial matrix to create DDW. This is why Dr. Doug Wallace has always found heteroplastic mitochondria seem to have water trapped in the matrix when he has examined it under electron microscope.
Normal ROS creation is only controlled when its quantized by the incident light at cytochrome 1 the NADH/NAD+ couple. It’s quantized only when ECT electrons and TCA protons are moving freely in the DDW crystalline water made in the matrix under the power of frequencies in sunlight.
Most biochemists are at a loss to explain hydrogen motions in a matrix and why they are key to understanding brain cancer. Today, I am going to solve for X and show you why being a clinician and understanding both bio-physics and bio-chemistry is a must in understanding the biology of any cancer.
SO WHY ARE KIDS GETTING BRAIN CANCER AT ALARMING RATES?
I need you to become inspired to look into the conformational change of the in biochemical pathways and in any receptors in any cells due to hydrogen and to deuterium fractions they contain (H+/D ratio). These changes change how bio-chemical pathways can or cannot function when the matrix can no longer recycle protons in the matrix. Remember Dr. Doug Wallace has taught us all that 85-90% of chronic diseases are mitochondrial, so what I am going to explain to you will explain most of those diseases as well. Yep, it is that big folks.
You have to begin to ask yourself to what degree does the amount of H+ and deuterium alter function and the exchange of H+ in glycolysis, TCA cycle, and in the PPP. When you do, it turns out, deuterium affects the observation of interactions/reactions that all biochemists take for granted. It uncovers their Dunning Kruger effect of bio-chemists for you all to see and why I have disdain in my heart for them.
The ATPase needs a chronic and fast source of H+ all the time to run the ATPase at 100% efficiency. Red light is the incident light source that pushes the protons between 600nm and 1600nm. It turns out 1538.5 nm is really important frequency for that proton electric current Becker found long ago to drive regeneration in mammals. It was confirmed by Del Guidice and Preparta in 2000.
HOW DID I FIGURE IT ALL OUT AS A BRAIN SURGEON?
I saw a massive increase in glioma’s at the end of my residency at LSU. So I asked a buch of bio-chemists why this might happen. Here is how the story unfolded.
Glutamine import and metabolism through the TCA cycle has been shown to persist under hypoxia/pseudohypoxic conditions. This told me that glutamine has to be important in a cancer state when it was clearly not important in a state where oxygen tensions were high. Remember what I have already taught you as members of jackkruse.com, namely that, low NAD+ = pseudohypoxia = Leptin resistance.
The bigger key for understanding this dicussion is that glutamine contributes significantly to citrate carbons in the TCA cycle pictured above. Why is this a big deal to us mitochondriacs? Why do biochemist food guru’s whiff on this insight?
One has to look at glycolysis differently if you are a mitochondriac or quantum biologist like we are. If you look at what happens to hydrogen’s only in glycolysis, from glucose to pyruvic acid conversion in glycolysis, before the TCA cycle entry as acetyl CoA, you will see the real function of the linkage to glycolysis and the TCA cycle in a living system.
Glycolysis is a “primer catalyst” (H+ exclusivity) reaction acting as a more “ancient dehydrogenase mechanism” to remove hydrogen atoms from specific carbons in glucose. It appears nature is particular. Living cells will chose to oxidize these dehydrated carbons once pyruvate enters the TCA later in the TCA cycle. This is conserved in the TCA cycle when acetyl Co is formed in the matrix. This tells us black swan mitochorndriacs that glycolysis is the older evolutionary system compared to the TCA cycle. When life was less complex it could live off a linear pathway. Now it cannot. It also means the TCA cycle is a new generation hydrogen furnace.
It is why the TCA cycle is a much more complex dehydrogenating conveyer belt, built into a cyclic format in the matrix instead of the older bacterial version of glycolysis that was in the cytoplasm and was a linear strand of bio chemical reactions. Stop. Where did a mitochondria come from? Bacteria. Thanks Lynn Marguilis. Mitochondriac lesson well learned.
This linkage is lost on most bio-chemists because of how they were taught. Remember all doctos learn bio-chemistry from them in medicial school so this is why most doctors are clueless about this too.
The specificity of carbon oxidation position is related to hydrogen position in glucose. Here we see the relativity of size and positon impact the thermodynamics of the cell. This tells the quantum clinician and the astute biologist to pay attention to why nature is using all these crazy steps to control enzyme kinetics in the matirx. It does not make sense unless you understand evolution. Nature is doing this quantum dance very carefully for a deep reason. If you are wise and a mitochondriac, you might learn something new about bio-chemistry that you never realized before. I did that day back in the late 1990’s.
The bio-physics of this hydrogen quantum dance underpins the pathways’ machinations (why there is so many enzymatic steps) and those moves are important for reasons that underpin the bio-chemists Dunning Kruger effect to fail to account for it in living cells. In fact, if you look close at these reactions you’ll see that enolase removes a H20 molecule from glucose in glycolysis. This is how a mitochondria reverses the photosynthetic reaction that consumes water in making glucose from CO2 and water.
This means the biochemist better understand the sun well too, or their algorithms will not make any sense if you just follow the substrates alone. That is all bio-chemists do. Most do not understand this nuance. I began to understand why young people were getting gliomas at faster rates that day. It took the literature 15 years later to prove my insights correct. See the study below.
This is why ALL cancers are always linked to poor solar exposure too in tissues. Sunlight’s frequencies are why this specificity matters in cancer. Sunlight uses non linear frequencies (UV/IR) to dictate the movement in hydrogen in bio-molecules using a molecular resonance mechanism I taught you in previous patreon blogs. This is why I am so interested in the physics of sunlight. Bio-chemists miss this quantum nuance and that is why they think pathways and substrates are all that matter. Not true.
How do I know I am correct? Well it links to this paper here. Under glucose deprivation in human cells are all pseudohypoxic to a degree. They then use glutamine to derived fumarate, malate, and citrate. They ARE significantly increased in these cases.
We know this from isotopic studies on carbon 13 flow in pathways. This isotope thing is a big deal folks. The Carbon 13 labeling patterns has demonstrated that glutamine is fully capable of generating an alternative energy-pathway in cells with a matrix that can no longer make DDW by using a glutaminolysis pathway involving a glucose-independent TCA cycle.
This is why the Warburg shift likes glutamine so much. It is a key source of new H+ for the TCA intermediates that are all deuterated by chronic blue light exposure via the eyes. Glutamine acts like methylene blue does in a matrix. It is capable of switching out heavy hydrogen for light hydrogen like Szent Gyorgi found back in the 1930’s. It lightens the load of the matrix of deuterium.
Erlenmeyer, Schoenauer, and Stillmann confirmed the vitamin C proton observations of Szent Gyorgi when they found in 1936 that during the establishment of the equilibrium reaction below:
Succinate + methylene blue = fumarate + leucomethylene blue
under the influence of deuterated succinic dehydrogenase, an exchange of the carbon – bound hydrogens of the succinate also takes place. In this way the “heavy” succinate gradually becomes “lighter.” The same thing was found in malate and fumarate too. This was the key old paper that told me the movement of hydrogen has to be specific and controlled by sunlight if we are to avoid oncogenesis.
Methylene blue (MB) performs best under red light frequencies when it is tested in the lab. It does even better in sunlight. Why is that? Sunlight is 42% red and this red light is the only light in the spectrum of the sun that is capable pf penetrating human tissue deeply to get to every mitochondria where hydrogen exists. Red light in the sun goes from 600nm-3100nm but our eye only sees 600-1000nm. Our mitochondria senses all red frequencies everywhere to control the flow of protons in cell water.
Glacial melt water has something in common with matrix water. It is how nature allows cells to control protons by making protons do something that the sun cannot control. Remember the photoelectric effect only allows light and electrons to work in unison. So cells decided to use DDW to make their EZ in the matrix the strongest it could be on Earth. Deuterium in water diminishes the size of the EZ. This is why, in my opinion, the matrix and chloroplast favor it. Gerry Pollack has never done this experiments to prove there is a difference in bulk and DDW, but others have done INS experiments that lead me to this conclusion.
If the EZ with deuterium is capable of excluding protons……..it really would exclude deuterium and this explains why life is the way it is. This is why the ATPase is prejudiced to the use of H+. Moreover, it explains why deuterium fractionation can be used as an optical switch to control growth and metabolism in the retina or open the door to mitochondrial diseases. Deuterium inflows radically alter the metabolic rate of tissues by causing small swellings in the mPTP pore. This area is normally protected by the EZ of the MINOS.
Methylene Blue is capable of performing substrate-level phosphorylation (SLP) by removing deuterium from the TCA intermediates and results in the production of ATP independent from the ATP synthase (ATPase). This means that MB can function outside the TCA cycle to lighten the hydrogen load when the matrix is weigh down with deuterium. Too bad oncologist do not know this, huh?
Bio-chemists never ask the simplest questions when they are faced with a clinical dilemna because they don’t observe nature well and they do not see or treat patients. DOCTORS DO. Have I told you that Albert Szent Gyorgi was a DOCTOR of MEDICINE? Below is a picture of someone who has no clue how to use MB correctly to repair these defects because his mouth should not be blue. Refuse to be ‘bullet proof’ and become a black swan mitochondriac instead. You’ll be a lot more wise. Most supplements and manufactured fats are all deuterium bombs.
Bio-chemists and many bulletproof bio-hackers rely too much on what other idiots have told them without looking why something really happens. Clinicians like myself do not do this because we see patients who have disease we cannot explain based upon what we were taught and we learned that when you do not know something you have to ask better question to figure it out. You must tap your curiosity to satisfy your curiosity’s hunger. When we want to understand why brain cancer is on the rise all of a sudden out of the ‘blue’, we ask questions of the bio-chemists teaching us. So I went to find a few of these guys in the medical school and I asked some questions.
I am a neurosurgeon who treats gliomas. These are horrible diseases for patients and surgeons. One thing I learned in medical school and residency is that glioma incidence in young people is rising fast. I ask why, and nobody seemed to know why. Then I found out these new glioma tumors are mostly spontaneous cases without any associated genetic defects. I found that curiosu consider oncology believes most cancer are caused by gene defects. I asked why. Nobody knew. Then I found out many of these de-novo gliomas all have links to other weird causes of familial cancer syndromes. I asked the bio chemists why this was the case and they did not know.
Then I went to the hospital and talked to the pathologists who did autopsy’s on these patients once they died.. I asked the pathologists why this set of circumstances was occuring in gliomas, and it was clear nobody had any answers for me. I asked why isn’t anyone studying this? I got blank looks from all the PhD’s. Bio-chemists only study what they can get $$$$ for and apparently none of them thought that these hydrogen movements in gliomas I found was big deal. I guess most of them thought it would be a tough sell to the NIH?
So in 2000, I opened up a bio-chemistry book and began to look for a pattern to explain this curious set of circumstances in brain cancer in young people. I found big clues in how hydrogen moved in glycolysis. What was the thing that caught my eye about this? Why does it take cells ten enzymatic steps to cleave 6 carbon sugar into two 3 carbon pyruvate when it appears way easier to do in a lab with a lot less steps? Then I asked why does it take 9 enzymatic steps to remove two CO2’s of molecules in the TCA cycle? That is when I realized why Szent Gyorgi and Pauling where so transfixxed on hydrogen biology and vitamin C in the 1930’s.
So I went and carefully read all their papers. I found my answer. The reason this was happening was a light effect. It was quantized, and it was tied to H+ movement, caused by solar frequencies that humans were no longer getting routinely.
I then found out that mutations of genes involved in the tricarboxylic acid (TCA) cycle such as fumarate hydratase, succinate dehydrogenase or isocitrate dehydrogenase 1 or 2 are causally linked to familial cancer syndromes (Bensaad et al., 2006) or spontaneous low grade gliomas and acute myelogenous leukemia (Dang et al., 2010). Then I answered my own question about why I was seeing milennials with spontaneous low grade gliomas.
I realized the environment we have built for modern humans today is not what it was in the 1930’s any longer. It is now like it is in a bio-chemsts lab, blue lit and filled with RF and microwaves. I went read about bio-physics of RF and microwaves on hydrogen and it was here I learned that RF radically effects H+ motions called precession in bio-chemical pathways. See, we neurosurgeons use MRI a lot, so I knew a lot about MRI’s already. In MRI image generation, we use pulsed RF frequencies to change the precession of hydrogen atoms in tissues to get images of the CNS. Most tumors show up on T 1 imaging by having an altered signal. The relaxing signal is different than regular tissues. I asked the radiologist why and they did not know. I figured it out by reading their literature. Deuterium is alters T1 imaging because of the kinetic isotope effect shields 96 H+ protons from this effect and this ruins our ability to see normal water protons. This is what we see in degenerative disc diseases cases on T1 imaging. This was how I figured it out. I started to notice all my patients had altered water content in their discs and complaining of muscular back pain. I realized that all patient with back pain were patients loaded with deuterium and this was causing imaging artifacts.
DOES FAKE FOOD AND GMO’S AFFECT GLIOMA’S TOO?
All fake foods made in a lab are made using hydrogenation. The process in a lab has no photosynthetic controls. Hydrogenation refers to the treatment of substances with molecular hydrogen (H2), adding pairs of hydrogen atoms to compounds (generally unsaturated compounds). These usually require a catalyst for the reaction to occur under normal conditions of temperature and pressure in a lab. Most hydrogenation reactions use gaseous hydrogen as the hydrogen source, but mitochondria and cells clearly have developed alternative sources do this as I am laying out very carefully. The reverse of hydrogenation, where hydrogen is removed from the compounds, is known as dehydrogenation. This is what cells to do foods as I showed you above in glycolysis. How cells do it is specific. Industry does it way different. Hydrogenation differs from protonation or hydride addition because in hydrogenation the products have the same charge as the reactants.
Hydrogenation reactions generally require three components: the substrate, the hydrogen source, and a catalyst. The same is true in a mitochodria or in a lab. How it occurs is the difference. In a lab of a big food company, the reaction is carried out at varying temperatures and pressures depending on the catalyst and substrate used. The hydrogenation of an alkene produces an alkane. The addition of hydrogen to compounds happens in a syn- addition fashion, adding to the same face of the compound and entering from the least hindered side. Generally, alkenes will convert to alkanes, alkynes to alkenes, aldehydes and ketones to alcohols, esters to secondary alcohols, and amides to amines via hydrogenation reactions.
The TCA cycle uses some of these reactions as the picture above showed.
Catalysts of Hydrogenation must be controlled by the matrix
Generally, hydrogenation reactions in a Bog Food lab will not occur between hydrogen and organic compounds below 480 degrees Celsius without metal catalysts. Mitochondria have iron and molybdenum (Mo) on the inner mitochondrial membrane. The use of Mo on this membrane is a remnant from its bacterial origins. I’ve written a whole blog on Mo fo rthis reason. It is a special transition metal. This is why the inner mitochondrial membrane, from and evolutionary perspective, is very different than the outer mitochondrial membrane which resembles a classic eukaryotic membrane which has no molybedenum in it. I’m surprised Nick Lane has not figured that one out yet to be truthful. Mo has a ton of electrons in it to help act as a catalyst at low pressures and low temperatures. In a Big Food lab catalysts are responsible for binding the H2 gas molecule. They do not screen their gas source for dueterium content. I’ve asked them. The catalysts they use facilitate the reaction between the hydrogen and the substrate (usually LA) used by the food company to create food. Platinum, palladium, rhodium, and ruthenium are known to be active catalysts which can operate at lower temperatures and pressures. In big food industry I found research is ongoing to procure non-precious metal catalysts which can produce similar activity at lower temperatures and pressures. They don’t seem to know about Molybdenum at all when I asked. It works at one atmosphere and body temperatures really well. It however, also doesn’t work as well in space, and this is why astronauts are getting sick as they enter space too long. They all come back with mitochondrial changes in their retina which I detailed in my Vermont 2017 talk. In space, their matrix cannot perform these hydrogen proton recycling reactions either as they can on Earth and NASA appears to be unaware of it.
Nickel-based catalysts, such as Raney nickel, have been developed, but still require high temperatures and pressures and these won’t work in space and they are too expensive for industry to make money from their cheap fake foods. All fake foods allow for a ton of deuterium to be added to their carbons. This is why fake food and GMO foods are to be avoided by mitochondriacs who understand that proton recycling is the key thing to get right in a matrix.
Heterogeneous Catalysis: The hydrogenation of ethylene (C2H4) on a solid support is an example of heterogeneous catalysis.
Catalysts can be divided into two categories: homogeneous or heterogeneous catalysts. Homogeneous catalysts are soluble in the solvent that contains the unsaturated substrate. In the fake food industry they use polyunsaturated fats as their substrate. Photosynthesis is a lot more discriminating in controlling hydrogen movement in the process as she makes her substrates for metabolism for oxidation in the matrix. This is why the matrix has so many unusual steps for glycolysis and for the TCA cycle.
Heterogeneous catalysts are found more commonly in industry, and are not soluble in the solvent containing the substrate. Often, heterogeneous catalysts are metal-based and are attached to supports based on carbon or oxide. The choice of support for these materials is important, as the supports can affect the activity of the catalysts and this is what affects ligher hydrogen or deuterium additions to the process. Hydrogen gas is the most common source of hydrogen used and is commercially available. Cells use hydrogen from the bio-molecules of glucose and fat as their source of hydrogen. All of these sources are processed by PHOTOSYNTHESIS!!! Those three pathways are called C3, C4, and CAM pathways and all of them have variable amounts of deuterium fractions in them as previous blogs have laid out. The TCA cycle is in charge of sorting through all these fractionations as this blog is laying out.
Hydrogenation is an exothermic reaction, releasing about 25 kcal/mol in the hydrogenation of vegetable oils and fatty acids in a lab. For heterogenous catalysts, the Horiuti-Polanyi mechanism explains how hydrogenation occurs. First, the unsaturated bond binds to the catalyst, followed by H2 dissociation into atomic hydrogen onto the catalyst. This is where deuterium can be added to the fake food. Food compaies do not fractionate their hydrogen gas because they have no idea nature does it in the water cycle that is one of the main substrates of photosynthesis because it consumes rain water which is deuterium depleted by nature.
In industry, then one atom of hydrogen attaches to the substrate in a reversible step, followed by the addition of a second atom, rendering the hydrogenation process irreversible in the lab. In the mitochondrial matrix, photosynthetic hydrogenation is reversible to C02 and DDW.
In the fake food industry for homogeneous catalysis, the metal binds to hydrogen and deuterium to give a dihydride complex via oxidative addition. The metal binds the substrate and then transfers one of the hydrogen atoms from the metal to the substrate via migratory insertion. Deuterium is far more reactive and this results in incomplete hydrogenation. This is a big problem for the final food product because it makes trans-fats which are not naturally found in eukaryotic membranes. Transfats do not work well with DHA in the lipid rafts electrically. Hydrogenation is important in processing vegetable oils because most vegetable oils are derived from polyunsaturated fatty acids of C3 plants. Partial hydrogenation reduces most, but not all, of the carbon-carbon double bonds, making them better for sale and consumption. The degree of saturation of fats changes important physical properties such as the melting range of the oils to create foods that last for ever on a shelf in a supermarket; an example of this is how liquid vegetable oils become semi-solid at various temperatures.
Incomplete hydrogenation of the double bonds in big food industry has health implications because of it deuteration; some double bonds can isomerize from the cis to the trans state. This isomerization occurs because the trans configuration has lower energy state than the cis configuration. This appears to be why nature spends so many steps on the processing of hydrogen in nature. The trans isomers have been implicated in contributing to pathological blood circulatory disorders like atherosclerosis and heart disease. The higher the deuterium fractionation in the fats the more wind up in arteries and more calcium build up occurs. This makes blood vessel less reactive to UVA light close to the surface of the skin and as a result the vessels make less nitric oxide (NO). Because the vessels make less NO, there is less vasodilation and as a result the blood pressure of patients rise. Most people with high deuterium fractionation in their tissues have high blood pressure, diabetes, obesity, and fatty liver with many deuterate triglycerides (TG) in their blood. The TG’s cannot be filtered by the liver’s ATPase because of doubled atomic mass so this is why visceral fatty liver develops. The cause of metabolic syndrome is a high deuterium fractionation usually above 130 ppm on breath testing. Here is a link that shows how electromagnetic fields lead to calcified vessels.
VIDEO OF SOMEBODY ELSE ASKING THE SAME QUESTIONS, but not understanding how it all fits together.
WHAT ABOUT THE nnEMF LINK TO BRAIN CANCER?
Microwaves are well know to vibrate and rotate the bonds in water and this causes heat release and oscillations of water. Mitochondria make water and they sit in the water they make. This means they way they move is affected by microwaves and this stops them from burning fat properly in the TCA. Then I relaized why everybody was getting fat before they got cancer. This is how microwave oven work, they jiggle the water in food to heat it. It turns our cell phones do the same thing in our brain when we put it up to our head. Then I read Frey and Addey work out of UCLA in the 1960’s that showed microwaves and RF cause upregulation of AMPk and blood brain barrier leakiness. This was repeated by Volkow in 2011. I realized immediately why technology was causing gliomas. It ruined how glycolysis and glutamine were feeding TCA intermediates and this in turn ruined hydrogen movements in cells. You feeling me now patrons?
