DECENTRALIZED MEDICINE #28: JABS/CANCER PART 2

If you looked at the video above you'll notice how light is contained in coherent domain water. The jabs cause less water production in cells and this allows the light normally harnessed in cells to leak out to the rest of the organ and this ruins the fidelity of photonic signaling and begins the process of oncogenesis.

Because each shot has 60 billion pieces of DNA protected in Liquid Nano-Particals (LNPs) this means rapid dielectric collapse can occur in the jabbed to lead to turbo cancer. My current concern as an MD, is it possible that creators of this bioweapon used the LNP delivery system to introduce these virus-sized transistors - perhaps even in a targeted way using specific LNPs? and if they did, what the f would be the effects? This is my current night mare.

Each shot has 60 billion pieces of DNA that can become part of your DNA, and it is more likely if the nuclear promotor SV40 is present in the jab you took. So, one of the things I need the jabbed to understand is that even if it is more probable than not that your DNA is going to be invaded, you have to do things to your environment to make it less probable that it occurs, and this makes oncogenesis less likely.

I want you to think of these pieces of DNA as matter. Then I want to remind you about the mass equivalence equation, E=mc^2

Since 1905, physicists have told us that the atomic quantum world does not act like the macroscopic world we experience regarding matter. Recall that mass and light are forms of energy that take shape, form, and size based on the electrical environment they sense.  The electrical environment in us is defined by the Coulomb charge.

HOW DO WE GO FROM THE COULOMB CHARGE TO DNA?

Throughout the cell cycle, the cell is constantly monitoring the volume of a cell by way of water in the cell. These water networks are directly tied to the mitochondrial matrix's ability or inability to make DDW.   If the cell does not reach the desired volumes required by Nature, the cell will be unable to progress to the next phase of the cell cycle. 

There is a G1/S transition “checkpoint,” which causes the cell to arrest at this intermediate stage, if adequate water volume is not reached. When a cell is arrested due to inadequate volume, there are two possible events: either the cell will leave the cycle and enter G0 step, and become a dormant, non-cycling cell, or the cell will be recognized as non-viable, and undergo mitochondrial-induced programmed cell death (apoptosis). This is good because defective cells have to be removed because they are more likely to become cancerous.

Altered water volumes also increase eNOS, which acts to increase albumin in our blood plasma and the Na /H+ transporter in cell membranes.  Cancer cells up-regulate sodium/hydrogen exchangers (Na+/H+ exchangers) because they are looking for light hydrogen in other pathways than the broken TCA matrix source.  Cancerous cells cannot harvest enough hydrogen from the TCA cycle. This means the cancer state is intimately tied to the inability to generate light hydrogen from the TCA intermediates.   The TCA cycle is no longer an effective cycle. The electric power stored in membranes tell the Kreb cycle how to react as we see below.

The key point for the jabbed to know, you cannot use the TCA cycle as it was intended to if you DO NOT SEE THE SUNRISE. IN CANCER STATES THIS IS WHY THE WARBURG SHIFT OCCURS. MEMBRANES ARE NOT GIVING METABOLIC PATHWAYS THE PROPER SIGNALS. This is why this slide exist below.

The implications of this if you are jabbed is simple. You have zero tolerance and must see sunrises daily. You also have zero tolerance for any light exposure at night if you are to avoid a cancerous transition. The TCA cycle makes more water from metabolism than any pathways in a human. As such it is the anti-cancer mode of living.

The Na+/H+ exchanger is a membrane-bound protein that transports one molecule of Na+ into the cell while effluxing one molecule of H+. Water passively follows Na+ (modern belief). Because cancer cells overexpress the Na+/H+ exchanger, they rapidly pump sodium into their cells. 

Water (non-structured from the ECF) passively follows the sodium, causing the cancer cells to swell.  The oncologist believes this happens because of the Na/H+ transporter, but it is really due to the loss of the net negative charge from a reduction in the number of coherent domains in cells.  This reduces the electrons a cell can harvest. Cancer cells are electron-poor, and this is why their Coulomb charge is lacking. Recall that sunlight in the UV and IR range builds large coherent domains, and their size directly affects the Coulomb charge.  That Coulomb charge is a synonym for your redox potential in the cell.  

As a result, all cancer cell lines are known to have a lower membrane potential due to the lack of electrical power in the cell.

Oceanic microstructures on Earth act a lot like plasma from the sun. Cellular microstructures act very similar to oceanic microstructures. We think about the ocean as a fluid, but fluids cannot be a plasma.  So what is a plasma?

Plasma is a highly electrically conductive state of matter with freely moving charged particles consisting of electrons, protons, and atoms stripped of their electrons called ions.  Contrary to commonly held beliefs, plasma does not act like a neutral gas. Plasma is usually described in space.  But they exist on earth.  Plasma cutters are used to cut thick metals in fabrication.  Plasmas behave and look different from other forms of matter; they tend to be cellular and clump together to create filaments.  Your DNA is such a filament.  Controlling this filament is the key to avoiding an induced TURBO cancer.

If you are jabbed, your job is to become a filament expert. Why? Your mitochondrial colonies controls the DNA filaments in you by controlling electric and magnetic flux in a cell. This can protect you or cause cancer.

A Birkeland current in the space around Earth is a plasma current that flows from the sun to the Earth along geomagnetic field lines connecting the Earth’s magnetosphere to the Earth’s high latitude ionosphere. We see these currents in Aurora at the poles and lightning strikes at lower latitudes. In the Earth’s magnetosphere, these plasma currents are driven by the solar wind and interplanetary magnetic field and by bulk motions of plasma through the magnetosphere.  These plasma flows are driven by convection, indirectly driven by the interplanetary environment at a particular time. The strength of the Birkeland currents changes with the solar activity and with collisions of the local magnetosphere.  Why is this important if you are jabbed? The jab lowers your own magnetosphere. This affects how you handle terrestrial sunlight. Why?

It follows that currents in our cells change with the solar activity on our surfaces.  It has also been shown that the mitochondria in our cells are quite responsive to the sun’s presence or absence.  This relationship makes it very likely that living things with mitochondria are sensitive to changes in plasma on the sun and Earth, too.  Our mitochondria seem to be able to sense these electrical changes by altering their respiratory proteins to these plasma displays. This alters the biophotons that cells emit. The lower our magnetosphere, the more biophotons we liberate. The more biophotons we liberate, the more cancer we are likely to get. This means living in places that have high magnetic flux is critical for the jabbed. It also means that they need to be close to terrestrial sunlight that has strong electric fields. These things are found inside the tropics and inside calderas of volcanoes or at black sand beaches. These regions fuel decentralized networks in your cells.

YOUR CHROMOSOMES ARE BIRKELAND CURRENTS SITTING IN PLASMA SEA OF WATER.

Current and flow are synonyms because they are linked to Coulomb’s law.  A plasma in motion = DC electric current.  So, one of the more important properties of a plasma is that it can conduct electrical current. Anything that generates an electric current must also generate a magnetic field at 90 degrees.  These currents are what RNA and DNA take orders from. This makes the key place to stop turbo cancers. Physics does this by forming current filaments that follow magnetic field lines. DNA is designed this way. Few see this fractal in Earth in our own DNA design. We can visualize this pattern when chromosomes align and split during cell division. Filamentary patterns are ubiquitous in the cosmos and inside our cells.  Filamentary patterns are found in nucleic acids and collagen, and those filaments are linked to the distances between mitochondria inside of cells, as I described in great detail in Ubiquitination 5 blog post at wwwjackkruse.com. The DC electric current of Becker is linked to regeneration. This implies that the jabs all reduce electric power transformation in cells to cause the damage we see in the aftermarket data of the mRNA jabs.

Most sugars are polar molecules, meaning they are also electrically charged. DNA’s backbone is made up of sugars. Cellular charge changes in all membranes when redox is low and cancer manifests because the lowered charge in the blood plasma is what stimulates the liver to make less albumin as a result the liver begins to focus on glucose metabolism and the oxidative branch of the PPP to rid the body of deuterium in 5 and 6 carbon sugars that make up every cell membrane in your body and all RNA and DNA to become electrically more efficient. Your job is augment these effects with sunlight and magnetism found in strong terrestrial light. This is why cancer rates are lower in tropical regions than they are outside the tropics. This is why if your jabbed you need to understand why this advice is something to consider in your journey as a GMO human now.

Everything in nature that is decentralized and healthy is organized by charge.  In the sea, the valence bonds inside between oxygen and hydrogen atoms give the oxygen a slight negative charge and the hydrogen a slight positive charge. In turn, polarized water molecules attract the negative and positive areas on the sugars, which makes them dissolve in water, whereas non-polar molecules will not.  

Consider olive oil, for instance, as an example in salad dressing. As the New Scientist article states in this HYPERLINK, some common phenomena are examples of the ocean’s gelatin-like substance. The northern Adriatic Sea turns to jelly every few years during algal blooms. However, the microscopic forces involved with the occurrence are not readily understood, nor is the way that the gel forms, in general.  

REDOX 101 EXPLAINED

Gerald Pollack has written another book on gels and their creation, and no with surprise to my readers, this ability is tied to the creation of what he terms an exclusion zone in water.  This links algal blooms to sunlight.  Exclusions zones are really coherent domains that are an oasis for electron liberation to be used by cells in redox fashion. These coherent domains only needs a hydrophilic substance adjacent to it to create a charge separation in water by sunlight.  Once this occurs, light can be captured in water and the coherent domains grows massively. This means the amount of electrons to be delocalized in cells to control biology is INCREASED. This is the basis of what your redox potential is at its core.  This is how a plasma is created from light within water to form initially.

A milliliter of seawater contains huge numbers of polysaccharide molecules that if “…untangled and lined up end to end, would stretch 5600 kilometers”.  One liter of sea water also has 10,000,000 viruses in it, loaded with DNA and RNA.  Most are destroyed in our gut but because the human gut is designed to be leaky by design some can get through to our GALT. This is how we evolve. These are the spare parts cells use to figure our environmental cues and how to adapt to them.

There are also chains of DNA, proteins, and other organic substances that provide a nutrient-rich environment for the organisms that live in the ocean. Now think back to the brain gut 2 blog I wrote long ago.  UV light and sea water make more viral particles in the ocean then there are stars in the known universe.  This would have created a lot of viral particles and bacteria in a sea water gel at one time.  Might this be the conditions required for endosymbiosis to occur? Might it also be the way to reverse man made interlaction to avoid turbo cancers?

How would you expect nature build a cell to respond to excessive light loss?  Might there be a mechanism tied to excessive ELF-UV release tearing through a plasma that might be re-purposed in some odd way to regenerate us? Why did Popp find all cancer lines release massive amount of light from their cells?  Why are mitochondria at this time all running on glucose (Warburg shift)?   

Did you know that when high energy photons are traveling through hot and sparse plasma (just like the interstellar medium or deuterium loaded water) they normally get redshifted without scattering light.  Did you know that?  Mother Nature does and that is why cancer cells are liberating light massively when water creation via the TCA cycle is absent. This means using IR-A and NIR light can augment a jabbed patient to help them regenerate because Mother Nature built cells to operate by charge and frequency at all times.  Even when someone has a new turbo cancer there is bail outs to help reverse the process because all of Nature is quantized.   She knew that red shifted ELF-UV light could be a bail out to increase the red activation of water.  This only works if the water is deuterium depleted!!!!! The TCA cycle is how you make this water.

We make our DDW in mitochondrial matrix (TCA).  This means the first step in any reversal should be to focus in on using light to augment proton recycling.  When we have too much deuterium  inside of us when we are leaking massive light back to the environment in any cancer state. Seeing sunrise frequencies most of the day is one way to recapture the ability to re-harness the TCA cycle to make DDW again.

SUMMARY

What few humans alive realize today is that the SV40 story from the polio jabs was initially a salvage operation to save humanity from the scourge of cancer that Dr. Alton Ochsner and VP Nixon knew were coming. They had to let the Louisiana delegation in the House and Senate know what really was going on in all the covert bioweapons labs on Prytania and Magazine Streets. None of this data wound up in any medical journals by the actions of the FDA in concert with VP Nixon. This is why @Kevin_McKernan or @P_J_Buckhaults could not access to this data. It was never published in the literature. It was hidden and censored. When the industrial military complex realized the life preserver (LINAC) they sent to Dr. Sarah Stewart and Dr. Mary Sherman actually made the cancers more lethal, then the DoD realized what the two doctors found. A way to weaponized viruses and vaccines. When I went to @RickRubin podcast (Tetragrammaton) two years ago and told RFK Jr that SV40 was found in the Pfizer jab his face went white.

He knew exactly what that meant. Prior to that day, he had no idea that the problem that Ochsner found in 1951 was now in the jabs given in 2021. That 70 year span was proof positive that the USA was using bioweapons against Americans. Remember the DoD distributed the jab not BigHarma. They were the drug dealers who took the orders from the cartels in the Pentagon. In essense anyone who supports the mRNA platform is wearing the epaulet of the DoD bioweapons program on their shoulders out in the open for everyone to see. This epaulet for me mimics what the MS 13 tattoos were used for to round up all the gang members by @nayibbukele in his Exception Regime. This is why I asked my Congressman Matt Gaetz from Destin to come El Salvador and learn how President Bukele cleaned up his country.

I believe @mattgaetz was the perfect guy to round up all the people in Congress wearing the epaulet of compliance to the jab program.