From the hijacking of bitcoin to the passing of the GENIUS Act, a deep dive in the Epstein files reveals Epstein’s fingerprints are all over the transformation of the global economy and our digital currency enslavement. Aaron Day joins us today to discuss “The Hijacking of Bitcoin,” his detailed and well-documented breakdown of how and why Epstein hijacked bitcoin.
Look for 15 years I have tried to educate you. THIS IS THE LAST TIME. So pay attention. Your Rockefeller education beliefs are all FALSE.
When dueterium leakage occurs into the matrix it stimulates cataplerosis in the TCA and the M1 Phenotype results. This process leads directly to the CDR too because tunneling speeds are destroyed. Here is where you, Peter D and your Rockefeller education screwed you. You know shit about tunneling speeds.
Quantum mechanics tells us according to the formula for tunneling, even a tiny increase in distance (measured in angstroms) leads to an exponential drop in energy efficiency and a massive spike in ROS = massive non coherent UPEs that are the hallmark of disease generation. this is why I showed you Picard picture on the change in IMJ geometry. When the IMJs change you know tunneling speeds have cratered. Deuterium’s KIE is a massive problem for tunneling speeds. But you and your food guru friends have no idea why.
Quantum tunneling is extremely sensitive to mass. Deuteriumhas double the mass of H+.
In the quantum world, as scale shrinks the effects become logrithmic because of the inverse square law. This means the effect of deuterium is off the chart. The doubling the mass of the particle attempting to “tunnel” across a gap doesn’t just slow it down, it makes the probability of a successful tunnel drop exponentially. This is not subject to your beliefs or your experts beliefs because these UNIVERSAL laws in physics true on Earth or another galaxy.
The Result: Electrons and protons “stutter.” This delay increases the “dwell time” of electrons on the respiratory chain, leading to their premature escape and the creation of Superoxide. This is a ROS. ROS makes UPEs. You have no clue what a UPE even is because you’re a food guru. It is a biophoton.
The ATP synthase, (FoF1), is a physical motor that spins at speeds up to 9,000 RPM. It is designed specifically for the “light” weight of a single proton.
The “Wobble” Effect: When a deuterium atom enters the top of the motor, the extra mass creates a mechanical imbalance, much like a lead weight on a high-speed fan blade.
The Breakdown: This “wobble” creates friction and heat, physically damaging the mitochondrial inner membrane and causing leakage of the proton gradient. This leakage is a primary signal that triggers CDR1, as the cell perceives a loss of “pressure” (voltage) and shifts into defense mode.
Deuterium in the matrix then causes the 25(OH)D Crash. Remember the VDR sits on the IMM as a brake for unfettered ROS/RNS production. Mitochondria rely on metabolic water production at CCO which is deuterium depleted. It is a highly structured, liquid-crystalline state of H2O. This type of water excludes solutes and anything over the size of a H+. This includes isotopes like deuterium which are double the size/mass of H+.
When any stressor hits the system, say like nnEMF light stress, nnEMF shrinks the EZ water layer through CCO dehydration . When this layer collapses, deuterium “leaks” into the matrix and the enzymes and causes the destruction.
As deuterium replaces protium in the water shells surrounding the CYP450 enzymes, the vibrational frequency of the enzyme changes. The enzyme loses its “quantum tune.” To compensate for the loss of mitochondrial efficiency caused by deuterium “pollution,” the body consumes Vitamin D at a massive rate to try and dampen the resulting ROS and stabilize the membrane.
Once deuterium pollutes the matrix:
OXPHOS fails: The motors are broken.
Cataplerosis is unleashed: The cell stops trying to make ATP and starts dumping TCA intermediates (like citrate) to create lipids for new membranes (to replace the damaged ones).
UPEs spike: The “friction” from deuterium in the nanomotors releases incoherent photons (UPEs), signaling to neighboring cells that the environment is toxic.
The unleashing cataplerosis should make you realize why the M1 (Pro-inflammatory) Phenotype is always the result:
Because the TCA cycle breaks at two SPECIFIC places (at Isocitrate Dehydrogenase and Succinate Dehydrogenase).
This causes a massive efflux (cataplerosis) of Citrate and Succinate into the cytosol.
Succinate then acts as a potent inflammatory signal, stabilizing HIF-1α and further shutting down oxidative phosphorylation (OXPHOS).
In this state, the mitochondria stop making “energy and hormones” and start making “defense signals and ROS.” the ROS makes non coherent UPEs and this causes all the diseases of man. You do not know this because you do not read shit about biophotons. Van Wijk and Popp have written careers on it while you wasted your time with your Rockefeller biochemistr retard PhD who knows none of this. This explains why our Vitamin D receptor sits on the IMM because it is a key regulator of this entire process. Melanin sits on the skin in cholesterol rafts capturing UVB light to stop this process. That is why the SUN heals it all and most of your bullshit beliefs are all linked back to Rockefeller solutions in centralized biochemistry and BigHarma. The VDR on our IMM trys to act as a “circuit breaker” for the CDR tied to deuterium effects in the matrix.
The “Sinister” Element of deuterium is an expansion of Mitochondrial Heteroplasmy = disease. See Doug Wallace. LEARN.
ANY increase in heteroplasmy = mitochondrial DNA damage.
nnEMF increases the distance between respiratory proteins on the inner mitochondrial membrane.
This slows down Electron Tunneling Speed (e).
According to the formula for tunneling, even a tiny increase in distance (measured in angstroms) leads to an exponential drop in energy efficiency and a massive spike in ROS = massive non coherent UPEs that are the hallmark of disease generation.
In metabolic terms, cataplerosis is the process of “draining” or siphoning intermediates out of the Tricarboxylic Acid (TCA) cycle.
Here is what that “unleashing” looks like in the body:
Siphoning for Survival (Biosynthesis): Instead of intermediates completing the full cycle to generate ATP, they are exported to create essential building blocks. This happens in cancers.
Citrate is pulled for fatty acid synthesis.
Alpha-ketoglutarate is drained to make amino acids or neurotransmitters.
Oxaloacetate is diverted toward gluconeogenesis to maintain blood sugar. This is why nnEMF raises blood sugar in stress response.
Preventing “Clogging”: Cataplerosis acts as a pressure-relief valve. If intermediates (anions) accumulate too heavily in the mitochondria, it can disrupt cellular function. Unleashing this process clears out the “sink” so the cycle can continue to process incoming fuel.
The Cost of “Unleashing”: Because the TCA cycle is a closed loop, removing these “rungs of the ladder” will eventually break the cycle unless they are replaced by a counter-process called anaplerosis (refilling the cycle).
Environmental Link: In your specific context, light stress from a move and heavy nnEMF is unleashing cataplerosis might be the body’s way of prioritizing oxidative repair or calcium buffering over standard energy production. It’s a “emergency mode” where the body spends its metabolic currency (like Vitamin D and TCA intermediates) to fix immediate damage. It really tells you how bad the place you went to was.
In short: it is your metabolism switching from “maintenance mode” to “construction/repair mode” because your body is sensing a cell danger response. What I am saying to you , is that your body “used what it needed in this moment,” but it left a collateral wake in your system. What are the system collateral effects? I am likely describing a massive decoupling event at the Cytochrome P450 (CYP450) level. why? When Fe in in its +3 state it cannot bind oxygen and P450 cannot make hormones = pregnenlone steal syndrome.
Hormone synthesis from cholesterol relies on the CYP450 (Cytochrome P450) family of enzymes, which are heme-containing proteins.
The Power of Heme: Heme is the “business end” of these enzymes, acting as a specialized scaffold for electron transfer. To function, it requires precise quantum coherence, which is the ability of electrons to “tunnel” and move in a wave-like, coordinated state.
UPE Disruption: Non-native EMFs (nnEMF) act as electromagnetic “noise” that disrupts this coherence. This triggers the production of non-coherent Ultra-weak Photon Emissions (UPEs).
ROS and Heme Damage: The resulting flood of Reactive Oxygen Species (ROS) from the mitochondria (the “danger mode” or CDR1) is highly toxic to “free” or loosely bound heme. When the heme center of a CYP enzyme is damaged or its electron flow is decoupled by ROS, the enzyme can no longer convert cholesterol into pregnenolone (the “mother hormone”), effectively halting the entire steroidogenic pathway at the source.
If the environmental signals (like high milligauss levels from nnEMF) are constantly triggering the CDR, the mitochondria stay stuck in a pro-inflammatory state (M1 phenotype) designed for defense, not repair. the M1 state is caused by non-coherent UPE signaling. This is why high nnEMF environments are deadly when you blow away your P450 system.
True photorepair healing requires moving from CDR1 (defense) to CDR2 (growth) and finally CDR3 (differentiation and restoration). A “toxic” environment, one with high nnEMF, poor light cycles, or chemical stress, acts as a persistent “block” that keeps cells from completing this cycle.
Mitochondrial Mosaics: Over time, staying in the same environment creates a “mosaic” of dysfunctional cells that have failed to complete the healing cycle, leading to chronic illness or reigniting the flame of disease.
This new move by Sarah Rogers is causing The Blob to have its most insane meltdown of the year. Here I cover a potential new initiative by the US State Department’s Public Diplomacy branch to begin funding charities and think tanks in Europe that promote free speech online and digital freedom, and the utterly empty arguments being made in response by the EU, Brussels & Shadow Diplomacy elements of our own NGOplex and CIA.
Mike Benz: Executive Director, Foundation for Freedom Online. Former State Dept Cyber. Author of the unpublishable monstrosity, Weapons Of Mass Deletion.
