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Tensegrity and Redox......

Discussion in 'Redox Rx' started by Jack Kruse, Sep 4, 2022.

  1. Jack Kruse

    Jack Kruse Administrator

    Today's PSA from Tensegrity 7: If you want real change you have to go for wisdom that is uncommon to modern humans, why? Society has become so synthetic and artificial that the truth now offends people.
    Fake light causes your mitochondria ECT to slow because the respiratory proteins enlarge to slow electron tunneling….…..when it slows you up regulate carbohydrate metabolism by way of AMPK pathways. All this from the change in frequency of light. The brain can not tell sunlight from blue light.......and ancestral health is unaware of this. You no longer can afford to be.
    Hemoglobin’s peak light absorption peaks at "280 mm 420nm 540nm and 580nm" and has a very sharp cutoff at 600 nm. This points out why green light spikes in fake light might be behind many blood disorders. This is why green and yellow wavelengths of krypton ion lasers peak at 531 mm and 568 mm respectively they almost perfectly match the absorption peaks of hemoglobin so these laser colors are used for coagulation of blood and blood vessels. These absorption peaks in hemoglobin are ideally match the spectral absorptions of the aorta where atherosclerosis predominates. These ideas go way past atherosclerosis. They reach all the way to neurologic diseases like tumors and to neurodegeneration too because of the effect on the SCN and the RPE and dopamine in the brain as I laid out in Ubi 24
    So what has Seneff et al. missed? Absorption spectra of the skin, aortic wall and cornea show us some interesting connections when we look at them all plotted together. In the visible range of light (sunlight). The absorption spectra of the skin is 20-30 times that of the cornea. The absorption spectra of the aortic wall exhibits VERY SIMILAR peaks as hemoglobin. This data has been published for years, yet no one seems to link them in coherent fashion. Parrish and Anderson from 1983, Keijzer et al. in 1989 and Eichler and Seiler in 1991 have all shown this. Seneff and her WAPF supporters wants to suggest to us all this is all about eating more foods with sulfur, but what good is that when your skin and eye are constantly getting overwhelmed with long wave blue light frequencies at night while getting no UV frequencies in the AM? That is a half truth Rx. Half truths lead to full lies. Sulfur without its catalyst light frequency is a losing biological battle; look again how the absorption spectra is in the cornea with respect to the skin. Long wave blue light destroys the signaling optically of the RPE at night. AM UV light stimulates it in the AM. If you live in the UK you are in deep because you cannot make D3 without UVB in the RPE of the eye. Note it is not a skin surface effect. It is a photo biologic one in the eye. Food can give you sulfur but you need the proper light signal to make use of it! Location matters.
    Seneff believes and has argued that an underlying deficiency in sulfated cholesterol, is due principally to insufficient dietary sulfur. I do not buy this. It is due to a lack of AM UV and too much long wave blue post sunset. I read the tea leave in a quantum manner not in a biochemical one. Many papers have shown that inadequate sun exposure to the skin leads, over longer timescales, to severe depletion of cholesterol and sulfate in many tissues. This loss is ADVANCED by blue light signaling after sunset. This is the world we live in today, because it is artificially illuminated. The result is worse when you add in mobile technology. We have created this world. This is why I see heart attacks in young people and carotid artery occlusions in 20-and 30 year old commonly today. This sulfur deficiency in cholesterol, chondroitin, and heparin becomes life-threatening with age in tissues and the blood plasma to eventually lead to an atherosclerotic plaque and a lack of blood flow and the development of pseudohypoxia that cause a loss of triplet superoxide production. UV sunlight causes triplet oxygen to form naturally in our atmosphere and in our retina. Check out Ubi 15 and the story on ozone. Missing AM UV light fast forwards the disease further and the tissues it occurs in ages faster and the patient dies sooner. This can happen in a vessel or in your brain depending upon the intensity of the nnEMF involved. It is a well-choreographed program for renewal of cholesterol that is sulfated by AM light. Seneff missed the point completely on superoxide. Singlet SO is a bad player most of the time, but triplet superoxide is the ideal player cells need to run the sulfation program in our tissues to work with IR and UV light in the AM to increase oxygen tensions and lower NAD+ in mitochondria. No one sees this but it is published in laser data and in Russia. I know it and you better. The Russian data on the correlation of oxygen availability, UV light, and triplet state SO is crystal clear to those who go deeper than just food. Seneff in her own paper says the following, "Unfortunately, there is necessarily collateral damage from superoxide exposure". That alone tells me she does not understand how light works at all in our eye. She thinks it is a food story. So do your ancestral guru's. Sorry, it is not and never was; for brain diseases and atherosclerosis it is a lack of AM UV light not a food story. Triplet state superoxide is required to oxidize the LDL and to catalyze the reaction that produces sulfate from homocysteine thiolactone.
    After absorption of UV light photons, the photosensitizer is first transferred to an excited singlet state by the quantized energy in the photon. Then 3 possible decay channels are possible according to QED physics. Again not subject to your opinion. These are natures rules embedded in the photoelectric effect. This is why quantum physics works on probabilities and not absolutes. The 3 cases are non radiative, radiative singlet state decay to the ground state, and intersystem crossing to an excited triplet state. The last one, may also promote a reaction leading to the singlet ground state by either non radiative decay or by radiative triplet decay. The radiative decays are called fluorescence and phosphorescence, respectively. Life time for fluorescence are on the order of nanosecond time scales where phosphorescence may last up to milliseconds or even seconds. According to Foote (1968), two alternative reaction mechanisms exist for the decay of the excited triplet state which are called Type 1 or 2 reactions. They are characterized by either the generation of free radicals (Type 1) reactions, or the transfer of excitation energy to oxygen molecules directly in a Type 2 reaction.
    During Type 1 reactions the triplet state next interacts with a target molecule or protein, other than oxygen. Stop and think about mitochondria now at cytochrome 1 and what should happen seasonally for mitophagy. This is why seasonal eating is advocated in my book and why ketosis year round is a bad idea. Type 1 reactions result in the release of free neutral or ionized radicals. We use these to signal in mitochondria. Further reaction with triplet oxygen may also lead to the formation of hydrogen dioxide or superoxide. Where have you heard that before? From me, and me alone. No one see both sides of the light story. Now you see why I see the world differently than your food guru's. We need more light guru's.
    In Type 2 reactions, the triplet state of the photosensitizer directly interacts with molecular triplet oxygen (3O2) which is then transferred to an excited singlet state of (1O2). During this reaction the electronic spins are flipped of the electrons in oxygen. Light does this not sulfur. Both reactions are designed to occur simultaneously but when the environment around a mitochondria is altered by pseudohypoxia the Respiratory Quotient can be altered dramatically. The reason for this is because all electrons in ECT are designed to move to oxygen for reduction. Their flow is 100% dependent upon the electron density, size of the respiratory chain proteins, and the amount of oxygen present at the end of the respiratory chain. (Insert Nick Lane's new book here) This makes pseudohypoxia within the mitochondria a very powerful environmental variable because it controls the pull of electrons in ECT. Insert David Sinclair's paper on NAD+ and pseudohypoxia here. Pull in ECT is measured in voltage. So pseudohypoxia means that voltages in mitochodria are falling and that means the magnetic field developed in mitochondria have diminished. If it declines it does not draw oxygen to it because O2 is PARAMAGNETIC. Excited singlet oxygen is very reactive and toxic. It leads to cellular oxidation, mitochondrial swelling and necrosis. Weishaupt in 1968 identified singlet oxygen as the TOXIC agent in photoactivation of tumor cells. Carotenoids in skin promote the toxic singlet oxygen to triplet oxygen which is harmless. Does the skin and retina have carotenoids? Yep. Now those who have listened to my September 2015 webinar should be getting where I am headed. Now, did you know blue light 410-500 nm increases singlet oxygen and decreases triplet? Did you know that AM UV light 270-390 decrease it? I told you that in Ubi 15. Did you know that diabetics, who all get atherosclerosis and most neolithic diseases have no measurable superoxide? I also told you in Ubi 5 and 6 why Jimmy Moore likely has none either. See now why SO too much blue light at night and not enough UV light in the AM, sulfur are really all linked to atherosclerosis? It is a disease of light not food. Only a small mind believes that precept. Here is nature's concepts for you to examine.
    With pseudohypoxia, we always see a lack of AM UV light and too much blue light exposure after sunset when we make singlet oxygen over triplet superoxide; that is the reason why diabetes and most anterior eye diseases are blue light over exposures and a lack of AM UV exposures. Nothing is what it appears when your beliefs are tied to food alone. This is why we see alterations in Vitamin A in the brain. Vitamin A turns over with RPE damage by PM blue light or a lack of AM UV light. When these two things exist we are using carotenoids up in tissues chronically exposed in blue light diseases or underexposed to AM UV light. Once they are used up there are severe downstream effects at the surface that causes deeper biochemical abnormalities in cells below. This singlet oxygen predominates in a microwaved blue lit world and you never see triplet superoxide again until you get rid of this bad mitochondria. This is why all disease must first attacked by changing your environment and not looking into your genome.
    It's time for you and everyone else to understand details matter in quantum biology. Note from above that hemoglobin has an absorption spectrum spike at 280nm? Why would it have that unless the environment provided it? The natural AM spectrum does this. when you know better you do better.
     
    John Schumacher and JanSz like this.
  2. Jack Kruse

    Jack Kruse Administrator

    The capacity for unique vision is the gift of exquisite observation. Look for the ridiculous in everything and you will find it when your mind is open. Being number one requires you to be odd. Many call me a freak because my perspectives are unique. I fell blessed being classified as unusual, for it taught me to see the world with different binoculars. Every villain to a paradigm is a hero in his own mind, but every hero is a villain to dogma.
     
  3. Jack Kruse

    Jack Kruse Administrator

    Sunset and sunrises are the kind of kiss that inspires stars to climb into the sky and illuminate your world. Follow the path that leads to wisdom. Only then, will you illuminate the way for yourself and for others
     
  4. Jack Kruse

    Jack Kruse Administrator

    We are more often scared and frightened than damaged from our current beliefs about our circumstance; and yet, we suffer more from the lack of our imagination than from reality of our current circumstance. Life is a canvas furnished by nature laws and
    embroidered by our own imagination. In the world of our imagination, all things exist and belong.
     
  5. JanSz

    JanSz Gold

    Being number one requires you to be odd.
     
    John Schumacher likes this.
  6. Jack Kruse

    Jack Kruse Administrator

    In the coherent phase of life, water molecules can oscillate between two electronic configurations in a phase with a resonating EMF. The native EMF's life couples to are from the sun and the Schumann resonance of the Earth.

    Albert Szent-Gyorgyi had already highlighted the importance of water for life in the 1940s and proposed that organized water existing close to surfaces, such as found in cell membranes, is able to induce a very long-lasting electronic excitation via resonant transfer of the different molecular species present in liquid crystals, thereby activating them and enabling their mutual attraction for reactions to take place. Linus Pauling felt the hydrogen bond was the key to understanding what Szent-Gyorgi was trying to convey. When electrons are added to surfaces they become more likely to capture photon energy due to the photoelectric effect.

    This makes these surfaces more hydrophilic and they form a new structural zone in water that atomically forms in water. This structure essentially is a charge separating zone that surrounds everything inside a cell. Without the water being made in the mitochondrial matrix nothing inside a cell works. Why? As water is missing so are its hydrogen bond numbers. As hydrogen bond numbers drop, statistically, then SNP, genes, and proteins cannot function as they should because they exclude everything larger than the size of a proton = the lightest isotope of hydrogen. Statistics = probability = quantum realm. Light hydrogen is just a proton with its electron stripped out. It is the currency of the ATPase in mitochondria. The key to physiological functioning in a cell is linked to the bond angles in the hydrogen bonds between SNPs/SAPs/genes/proteins inside a cell. Because the electronic zone excludes the proton's positive charge, this zone has a large net negative charge as a battery would. Sunlight + coherent water becomes a battery for life. Without the battery, SNP/SAP/genes/proteins do not work. This is why you must fix the mitochondrial water creation mechanism to help people to health. This quantum dance forms the basis of your redox power. Quantum coherent water = water in its atomic construction. The hydrogen bonds are the pot of gold for health.

    This poses the question, how does the sun sculpt life?

    https://www.patreon.com/posts/71552008
     
    John Schumacher likes this.
  7. JanSz

    JanSz Gold

    How much (liters or kilograms) matrix water healthy human goes thru over 24hrs?

    Dr Boros claims that it is about equal to the volume of blood going thru the heart.

    Others (Wiki) say that body goes thru the weight of ATP equal to the weight of the whole body.
    Assuming that H contained in that amount of ATP is included in matrix water at some times,
    I calculated the amount of that water.
    It is still a lot but much less than Dr Boros says.

    ........................
    @Jack Kruse
     
  8. Jack Kruse

    Jack Kruse Administrator

    Boros is telling half-truths. Marketing is legalized lying. He has ownership in these water companies and centers. Some of my former members work for him now. This question cannot be known without knowing the precise heteroplasmy rate and potassium levels at the time. I keep telling you he is a marketer/scientist. Vet and parse his words carefully when profit is involved. This does not mean his science papers aren't valid. It just means how he profits from his research needs careful due diligence.

    Here are the scientific facts we know to be true today: Water makes up 99% of molecules in every cell. Water is a very small molecule that has more hydrogen bonds in it than any other compound. Liquid water contains the densest hydrogen bonding of any solvent, with almost as many hydrogen bonds as there are covalent bonds in its structure found anywhere on Earth. Water's hydrogen bond network changes at a pico and femtosecond level in any environment. Inside a cell, its atomic arrangement is controlled by electrostatic forces in a cell created by the redox power of the mitochondria in that cell. These hydrogen bonds can rapidly rearrange in response to changing conditions and environments (for example, solutes like K+ in a cell).

    This is why small atomic radius atoms like K+ change what water in a cell can do inside our cell membranes. The water inside a cell is not like the water humans sell. Water in a cell is an electromagnetic capacitor for sunlight because of how sunlight alters the hydrogen bonds in water. The most common small cation in a cell is K+. K+ has massive effects on the water made inside a mitochondrion at cytochrome c oxidase which sits right before the ATPase. What does sunlight do to these hydrogen bonds inside cells with respect to K+ concentration? The addition of the small atomic radius of K+ makes water liquid crystalline inside the cell. This means its physical, electronic, and refractive index varies. What is the stoichiometry of K+ to water in mitochondria that is working fine between -300mV to -400Mv redox state?


    Experiments by Ling have shown that each molecule of ATP in a cell controls 8,800 water molecule binding sites and 20 potassium ions to allow water to become structured inside every cell of your body. As redox varies so does the K+ concentration and # of water molecules created by mitochondria. Melatonin, NAD+, CO2 all vary in the same way as potassium does to redox power inside a cell. Environments change redox power by varying the charge density of the hydrogen bonds in water that mitochondria create.
     
  9. Jack Kruse

    Jack Kruse Administrator

    Go read the current blog series on charge density now. Put it together because Im spinning you're ATPases like mine now. JS seems to think my ATPase is suffering. LOL
     
  10. JanSz

    JanSz Gold

    My question is:
    How much (liters or kilograms) matrix water healthy human goes thru over 24hrs?

    current blog series does not have that value

    /////////////
     
  11. Jack Kruse

    Jack Kruse Administrator

    Society has become so synthetic and artificial that the truth now offends people.
    Artificial light or any light outside the visible causes your mitochondrial heteroplasmy rate to rise because the respiratory proteins enlarge to slow electron tunneling and decrease the amount of ATP made….…..when ECT slows and NOT enough red light is present shinning into your body to your mitochondria you up regulate carbohydrate metabolism by way of AMPK pathways. This means your blood glucose rises irrespective of anything eaten. All this from the change in frequency of light changes the charge density of things in your cell as your redox level has dropped.

    The brain can not tell sunlight from blue light.......and ancestral health is unaware of this. You no longer can afford to be.

    Hemoglobin’s peak light absorption peaks at "280 mm 420nm 540nm and 580nm" and has a very sharp cutoff at 600 nm. This is why RBC are red. They reflect all the red light above 600nm light.

    This also points out why blue/green light spikes in fake light might be behind many blood disorders. This is why green and yellow wavelengths of krypton ion lasers peak at 531 mm and 568 mm respectively they almost perfectly match the absorption peaks of hemoglobin so these laser colors are used for coagulation of blood and blood vessels. These absorption peaks in hemoglobin are ideally match the spectral absorptions of the aorta where atherosclerosis predominates. These ideas go way past atherosclerosis generation.

    They reach all the way to neurologic diseases like tumors and to neurodegeneration too because of the effect on the SCN and the RPE and dopamine in the brain as I laid out in Ubi 24

    So what has Seneff et al. missed in her work? Absorption spectra of the skin, aortic wall and cornea show us some interesting connections when we look at them all plotted together in the visible range of light (sunlight). The absorption spectra of the skin is 20-30 times that of the cornea. The absorption spectra of the aortic wall exhibits VERY SIMILAR peaks as hemoglobin in RBCs. This data has been published for years, yet no one seems to link them in coherent fashion.

    Parrish and Anderson from 1983, Keijzer et al. in 1989 and Eichler and Seiler in 1991 have all shown this. Seneff and her WAPF supporters wants to suggest to us all this is all about eating more foods with sulfur, but what good is that when your skin and eye are constantly getting overwhelmed with long wave blue light frequencies at night while getting no UV/IR frequencies in the AM?

    That is a half truth Rx. Half truths lead to full lies. Now you know why replacing water soluble B vitamins is a waste of time. Without its hydration cage it is doomed to fail. Just as sulfur without its catalyst light frequency is a losing biological battle; look again how the absorption spectra is in the cornea with respect to the skin. Long wave blue light, RF/microwaves all destroys the signaling optically of the RPE at night. AM UV light stimulates it in the AM. If you live in the UK you are in deep because you cannot make D3 without UVB in the RPE of the eye. Note it is not a skin surface effect. It is a photo biologic one in the mitochondria of your eye that has a problem because your clock mechanism is located there.

    Biological clocks are built as a flow meter for entropy inside of cells. Potassium orders water molecules by hydrogen bonding network cooperation. Entropy is a measure of the disorder or chaos in a system,and the more ions present in a solution the more disorder there will be. Solids have the most order and least entropy. They are held in a crystal lattice or network. The water molecule is quite small but the hydrogen bonds inside water are even smaller and most important to accurate biological clocks = ideal periodicity

    Food can give you sulfur but you need the proper light signal to make use of it! Location/latitude matters because that creates the water you need and makes your hydrogen bonding network to make your clocks uber accurate.
     
  12. Jack Kruse

    Jack Kruse Administrator

    you don't even realize I already answered it above. As your friend JS who thinks I am falling apart. Let's check his brain function out.
     
  13. Jack Kruse

    Jack Kruse Administrator

    Tell me JanSz what is the relationship between K+ and diabetics?

    When their K+ levels are too low, their pancreas makes less insulin. Did you know that? Might the level of insulin made have something to do with if they are skinny or fat? When insulin varies so does blood sugar. Does glucose change the charge density of RBCs? Does this change their optics? Studies show that people with low potassium levels release less insulin, have higher blood sugar levels, and are more likely to get type 2 diabetes than those with normal potassium levels. Did you know that?


    Potassium, both serum levels and to a lesser extent dietary intake levels, has been associated with incident diabetes. Lower levels of potassium have been found to be associated with a higher risk of diabetes. Few seem to understand how this links to biological clocks........Do you yet? If you do you will see your question has been very accurately been answered.


    https://medicalxpress.com/news/2022-08-insights-retinal-neurons.html
     
  14. Jack Kruse

    Jack Kruse Administrator

    What causes low potassium levels in diabetics?


    Low Potassium Levels in Type 1 Diabetes

    Low potassium levels are associated with a complication of Type 1 diabetes, called diabetic ketoacidosis. It is a condition in which your body does not make enough insulin to transport glucose into the cells, so the body uses fat as an energy source.

    Type 1 Diabetics tend to be skinny

    Now, what about type 2 diabetics?
    The Link Between Potassium and Type 2 Diabetes

    Potassium is generally stored in the fluid inside of the cells, but when there's too much glucose outside of the cells (blood sugar is too high), potassium moves OUTSIDE of the cell, raising potassium levels in the blood. Tell me JanSz what does this do to water inside your cells? How about your biological clocks?
     
  15. JanSz

    JanSz Gold

  16. JanSz

    JanSz Gold

    Ok. Let's check brain function.

    But I am more interested in your nose burns.
    To hopefully prevent that I use MT-2 (Melanotan-2) injections.
    How do you feel about me doing it?

    @Jack Kruse
    .............
     
  17. Jack Kruse

    Jack Kruse Administrator

    Nose wasn't burned. It was from a fight in Bahamas.
     
  18. JanSz

    JanSz Gold

    you said:
    raising potassium levels in the blood.
    --------

    Where in the blood?
    Serum?
    RBC?

    ////////////////////

    @Jack Kruse
     
    Last edited: Sep 14, 2022
  19. JanSz

    JanSz Gold

    I do not want to see your opponent's face.

    //////////

    What about me using MT-2?

    @Jack Kruse
    .
     
    Last edited: Sep 14, 2022
  20. JanSz

    JanSz Gold

    JanSz said:
    My question is:
    How much (liters or kilograms) matrix water healthy human goes thru over 24hrs?
    /////////////
    Indeed, I do not.
    But now I know that you know that value.
    .................
    @Jack Kruse
     

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