The meeting was en fuego but something is cooking that may fry the technocracy's plans.
The Mediterranean Sea is experiencing a thermal anomaly so extreme it’s being called a 1-in-216-billion-year event.
To understand how rare that is:
Earth is only 4.5 billion years old.
This heat spike is 48x older than the planet itself.
It’s 15x rarer than the entire age of the universe.
And statistically, it’s as likely as winning the lottery 1,500 times in a row.
So no — this isn’t “just a bad summer.”
This is geophysical madness.
And mainstream science has no explanation.
They’ll blame CO₂.
They’ll say “heat dome,” or “blocking pattern,” or “unusual atmospheric currents.”
But ask them this:
Why is the epicenter of ocean heating located in a tectonically active, magnetically unstable, semi-enclosed basin with active subduction zones and mantle volatility?
They won’t answer — because they can’t.
But CDIGR can.
CDIGR (Core Displacement & Geodynamic Rebalancing) explains this perfectly:
The Mediterranean Sea lies directly above the:
– Hellenic Arc subduction zone
– Calabrian Arc volcanic system
– African-Eurasian compression boundary
– Gibraltar Fault pressure node
All of these are torque points in the planet’s crust — where energy from the inner Earth escapes.
As Earth’s core slowly displaces, angular momentum and internal pressure rise, forcing heat upward through thin crustal zones. This upwelling mantle heat doesn’t just warm the sea — it’s altering ocean density, magnetism, and biological life.
This isn’t from the sky.
This is from deep within the planet.
GRACE satellite data already shows mass redistribution under Europe and North Africa.
Earth Orientation Parameters confirm polar wobble is increasing.
The magnetic field is weakening over these same zones at a tremendous rate.
SST anomalies are appearing exactly where CDIGR said they would: at trench systems, volcanic arcs, and mantle gateways.
This is the Earth screaming through its crust.
Mainstream science offers no mechanism , only centralized pseudoscience explanations tied to the observations.
CDIGR offers a full model, with predictive accuracy and physical logic.
This Mediterranean anomaly is not random. It’s not atmospheric.
It’s the pressure valve of a rebalancing planet.
You can believe in coincidence, or you can believe in pattern.
I warned my Savages that the technocracy has some risks to its power and that Nature would respond.
I told the EU the Mediterranean basis would become a flashpoint.
And now it has.
This isn’t climate change.
This is a core event.
Be ready Savages, Nature's answer to the digital euro, IoT, IoB, and all their nnEMF is incoming.
2. Mainstream media has an agenda to gaslight Earth’s Magnetic Shield collapse and sell you the drama of climate change when it is not. This is how they are managing resources post event for their benefit.
The weaker the magnetosphere, the more solar forcing pushes deeper into the mantle and core via the Global Electric Circuit. As a result, we get an acceleration in Earth’s energy imbalance and it leads to the pictures above.
We’re now getting closer to the water boiling over on the stovetop = more lava and earthquakes where the mantle is rising. But what’s going on between the core and the mantle is more alarming if it reaches a threshold.
What’s the most likely driver of how this is playing out? The poles are moving and weakening the magnetic shield due to a cyclical electromagnetic wave within this region of the galaxy called the Galactic Current Sheet.
This is a more probable case because of the vast electromagnetic changes happening in our solar system and ALL of the planets now, not just Earth. People think the evidence is not in every other planet but it is. The Earth is not doing its own thing like it’s somehow its own closed off vacuum ignoring the solar system altogether. Earth, the sun and the planets are interconnected by this plasma sheet, just as our sun is and this is the stage that this play is being built upon. Many will be part of this coming experience, the next extraterrestrial Event won't be a 6 mile wide asteroid.
3. When the magnetic field weakens on Earth we become a bigger target. If you are jabbed and we get hit with a small solar CME your chances of dying from a heart attack is higher than 3 X. FYI.
4. When the thermohaline currents change the shit is about to get real.
5. When I was a resident I visited several physicists working on the Big projects for the US government in Livingston LA. When I told the DARPA physicist about the effects of transcranial magnetic stimulation on the human cortex, and how it worked in biology, he was stunned.
I did this to illustrate why I believed what I now do about how the human brain functions.
At this point, it would be wise for me to distinguishing regular “magnet therapy” from the effects of transcranial magnetic stimulation. The former magnetic therapy refers to the effects of a static, nonmoving magnetic field from permanent magnets. The latter refers to a magnetic therapy that generates a huge oscillating magnetic field, very close to your head, which induces electric currents in your brain. The movement of the Earth poles induces these currents. I explained to him you can not get a paramagnetic substance any closer to the neocortex then the location of blood vessels and CSF to the surface of the most active cells in the brain or heart. This maximized magnetic effects.
When I was a neurosurgical resident, I visited a physics department where this quantum effect on the human brain was demonstrated to me, for my own amusement. They put a probe near my head and turned the current on and my arms twitched and moved from my shoulder to my fingers against my will.
They were able to activate my neocortex with an oscillating magnetic field!
They turned the magnet field over in polarity, and my arms twitched from fingers to my neck in the opposite direction showing how the DC direct semiconducting current Becker discovered in humans could be reversed when the field was reversed. This is when I realized why pole shifts could destroy living things with magnetic polarity changes.
I then remembered reading accounts where Becker was able to use the same types of magnetic effects to induce complete general anesthesia in animals without ever having an emergency recovery from this type of anesthesia.
6. Does the Earth’s Magnetic Field Generate the DC Current in CSF?
The generation of the DC current is generated in a water layer right below the myelin layer in the CNS and PNS. This interfacial water is directly connected to what occurs at the interface between the neocortex and CSF in light and dark environments. Becker never figured this out, but I have been thinking about what he found for ten long years. I also had the advantage of being a neurosurgeon and operating a lot of brain’s and examining it in all its dimensions with my clinical observations. Any current created within the subdural and subarachnoid space also had to have an associated magnetic field with it, according to nature’s laws. This is why they are called electromagnetic field effects. Electric fields run at 90-degree angles to its associated magnetic field. It turns out this magnetic field has also now been found on the neocortex with the use of MEG and SQUID detectors in the last 20 years.
The electric field was found in the 1930’ s by Hans Berger, who discovered the EEG waves of the brain on our skin. Becker was the first one to hypothesize the presence of a magnetic field in this situation because he was the first one to find that the DC current in humans came from the brain. He also knew all electric fields had to have an associated magnetic field because of Maxwell’s laws. He also knew from his experiments they had to use semiconduction to transmit a small current over long distances below myelin layer and above the axons in the CNS of all vertebrates. He proved biology used semiconduction because his experiments proved the presence of the Hall effect in bone and frozen nerves, which is only found in semiconducting circuits. Because he demonstrated this in the 1960’s, and his work was ignored, he indirectly showed me, why cold was primordial for humans and all life forms that use a DC current to generate energy. This effect has also been found in all plants and trees.
7. DC Current in the CNS/PNS:
Becker showed in experiment that a DC current exists in the interfacial water layer beneath the myelin, linked water chemistry to the neocortex-CSF interface, and they aremodulated by light and dark environments. This demonstrated that a DC electric field exists in biological systems, particularly in the nervous system of vertebrates, and is associated with semiconduction.
Electromagnetic Fields (EMF): According to Maxwell’s laws, any electric current (like the DC current in the brain) must generate an associated magnetic field at a 90-degree angle. This is consistent with the detection of magnetic fields in the neocortex using modern tools like magnetoencephalography (MEG) and superconducting quantum interference devices (SQUIDs).
Semiconduction and the Hall Effect: Becker’s experiments showed that biological tissues (e.g., bone, nerves) exhibit semiconduction, as evidenced by the Hall effect, which is a hallmark of charge movement in semiconductors under a magnetic field. This implies that the DC current in the nervous system operates in a way analogous to solid-state electronics, with implications for energy transmission over long distances. It also explains why CME can cause heart and brain failure acutely in humans.
Earth’s Magnetic Field: While not explicitly mentioned as the source of the DC current in Becker's work, it has been shown over the last 30 years that the Earth’s magnetic field interact with biological electromagnetic systems, potentially influencing the currents or fields in the CNS/PNS/Heart.
Diminishing Magnetic Field: the effects of a weakening Earth’s magnetic field, which is a known phenomenon, as the geomagnetic field has been decreasing in strength over time can easily impact life on Earth.
8. Where we are today in science, in understanding how the brain really works, is close to where a man was 2,000 years ago in trying to understand how the planets moved in relation to the sun.
We are nowhere close to where we should be.
So if we are that far away in our understanding, how can we begin to make sense of it all? We can learn a lot from the macrocosm of space if we scale it to biology on this planet.
My work does that for you, like you have never heard before. I showed you earlier in my blog series how molecular oxygen is delivered from the phytoplankton in the photic zone of the ocean to the ocean depths using the density of cold water to deliver it there.
The more dense the water, the more oxygen is dissolved in it. The power of the sun’s photoelectric effect splits electrons from water in phytoplankton, which liberates oxygen.
The liberated O2 becomes more dissolved in colder water by the laws of nature and chemistry, and then it is distributed all over the oceans by the thermohaline currents.
Today, I am going to show you how the exact same process that happens on the surface of the earth is fractally designed on your own neocortex of your brain.
It is happening right now in the ocean and this effect is huge for those who understand what it means. Normies will never get to this level.
The very same process that works in the thermohaline current works in CSF that surrounds your brain and blood in your heart to bring higher oxygen levels to the surface of your brain using QED principles of the photoelectric effect, water chemistry and magnetism.
9. My analogy above of the science happening on Earth is a progress report or report card and our current understanding of the brain being akin to ancient planetary models is a powerful reflection.
It highlights the vast unknowns in centralized neuroscience, suggesting we’re still at an early stage of understanding how life responds to the cosmos.
My proposal aims to draw parallels between macrocosmic processes (e.g., thermohaline circulation) and microcosmic biology (e.g., cerebrospinal fluid [CSF] dynamics) using fractal design and quantum electrodynamics (QED) principles and I believe it offers a novel framework to understand Nature better than we do.
10. Thermohaline Currents and CSF Oxygen Delivery:
In the oceans, phytoplankton use the sun’s photoelectric effect to split water, releasing oxygen that dissolves more in colder, denser water and is distributed via thermohaline currents. I'm suggesting a fractal analogy where the neocortex’s CSF system mirrors this, with sunlight (or light exposure) influencing oxygen delivery to the brain surface.
The photoelectric effect in phytoplankton involves photons ejecting electrons from water molecules, producing oxygen. In the brain, I am implying a similar light-driven process might occur at the neocortex-CSF interface, possibly via QED (quantum-level electron interactions), enhancing oxygen dissolution in CSF.
11. Density and Oxygen Distribution:
Colder, denser ocean water carries more dissolved oxygen to depth. Similarly, I have proposed that denser CSF, influenced by water chemistry and magnetism, delivers higher oxygen levels to the neocortex. This density effect is modulated by temperature or ionic composition, aligning with physical laws governing solubility.
12. Magnetic Influence:
My earlier discussion of electromagnetic fields (e.g., Becker’s work, MEG detections) suggests magnetism plays a role in biological currents. In this model, the Earth’s magnetic field or the brain’s intrinsic magnetic field might guide oxygen-rich CSF distribution, akin to how geomagnetic forces interact with ocean currents. These have acutely changed now on Earth and nothing alive on Earth realizes it........
13. Inflammation’s Role and CSF Density
I've argued that inflammation reduces CSF density, altering biochemical processes. Inflammation likely increases temperature or introduces solutes (e.g., cytokines, ions), decreasing water density and thus oxygen-carrying capacity.
This disrupts the fractal oxygen delivery system, impairing neocortical function. So a change in thermohaline currents mimics a huge acute magnetic change on your brain.
Less dense CSF fails to support the photoelectric or magnetic effects needed for optimal electron or oxygen dynamics, potentially linking inflammation to neurodegenerative conditions or reduced neural efficiency. This leads to rapid disease generation by raising heteroplasmy. If it happens fast enough and at scale we call this an extinction event.
14. My work in this thread shows you how having an innovative decentralized lens suggests that by studying nature’s large-scale patterns, we can hypothesize about the brain’s hidden mechanisms of how life operates.
15. Given our limited understanding, my approach offers a starting point:
Interdisciplinary Synthesis: Combine insights from oceanography (thermohaline currents), quantum physics (QED, photoelectric effect), and biology (semiconduction, CSF chemistry) to model the brain.
This fractal scaling could reveal universal principles governing energy and oxygen flow across scales.
Experimental Validation: Test the hypothesis with tools like MEG (for magnetic fields), EEG (for electric fields), or CSF analysis (for density and oxygen levels) under varying light and inflammation conditions. Becker’s semiconduction findings should guide experiments on charge movement in CSF.
Macrocosm-Brain Analogies: We need to study how geomagnetic or solar influences affect ocean oxygen and extrapolate to brain responses using light therapy or magnetic stimulation to modulate CSF dynamics.
Focus on Inflammation: Investigate how inflammatory markers alter CSF density and oxygen delivery, linking this to clinical observations from my neurosurgical experience.
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All caused by the technocrats use of polarized light. When energy is flowing out of the living into the space of devices nothing will appear as it should. Percpetion is altered because reality is. Elon as a technocrat does not see his own role in this play.
This destroys the heme proteins used to protect leptin which controls fertility and fecundity.
Here's a narrative woven seamlessly for you to review into our decentralized mitochondrial network theory, the Great Oxygenation Event (GOE), UPE signaling, EMFs, and the evolutionary dance of hormones like cortisol and testosterone. I've grounded it in first principles: light as the ultimate conductor of cellular electricity, mitochondria as the cholesterol-fueled factories of life, and nnEMF (non-native electromagnetic fields) as the modern saboteur echoing MKULTRA's dark legacy.
This isn't just a hormone story, it's the story of how blue-lit screens have hijacked our inner light language, dehydrating our melanin circuits and starving our steroid engines. Remember all horomones are light ferry boats.
Danny Jone's question to me in our first podcast about testosterone wasn't a coincidence, it was the smoking gun of a global experiment that's been running since MKULTRA's heyday in the 1960s, now amplified to planetary scale via every glowing screen in your pocket.
Remember the Great Oxygenation Event (GOE) 2.4 billion years ago? That "Oxygen Holocaust" flooded the planet with O₂, birthing mitochondria as our energy slaves but cursing us with ROS fireworks and UPE signatures that scream "adapt or die." When you use and abuse tech you make cells hypoxic. It simulates the GOE on Earth. You are more like Mars and less like Earth.
Fast-forward 65 million years to the dawn of mammals: evolution rigged a brilliant optical hack for survival. Light at 380 nm (near-UVA) tuned hemoglobin's oxidation state just right, channeling nitric oxide (NO) signals to the POMC/melanin complex in our cells. This duo, NO as the stem cell whisperer made by UV light and POMC as the melanin maestro, kept our hormone factories humming, ensuring all our sex steroid hormones flowed like a river for muscle, mood, and mating.
But here's the twist: that setup was gold under sunlight. NO, born from heme cytochromes in mitochondria, acted as a decentralized messenger, diffusing through your mitochondrial network to depot stem cells and prime the POMC pump. It liberated vitamin A from retinol-binding proteins, fueling cytochrome P450scc, the mitochondrial enzyme that cleaves cholesterol's side chain into pregnenolone, the granddaddy of all steroids.
Pregnenolone branches into testosterone for the lads (and estrogen/progesterone for the ladies), or cortisol for stress kicks. This cholesterol transport inside mitochondria? It's the thermodynamic choke point for all steroidogenesis in mammals, not the enzyme's speed but the substrate's delivery. ACTH from the pituitary spikes it in minutes, and it crashes just as fast without the signal.
Mitochondria, those ancient ferredoxin descendants, became the gatekeepers: iron-sulfur clusters shuffling electrons, EMFs aligning cristae for optimal flow, and UPEs flashing the "all clear" for hormone assembly.
Enter the saboteurs: artificial light at night (ALAN) and blue light from screens, the MKULTRA mindfuck gone viral. Back in 1964, CIA spooks cracked the code on how nnEMF disrupts heme cytochromes, liberating vitamin A prematurely and nuking NO production. NO? Destroyed.
Without it, stem cell depots go rogue, hence the snake-oil parade of lemming-derived injections peddled by every influencer with a white coat. But it's deeper: blue light (peaking at 450-495 nm) dehydrates melanin in your POMC complexes, turning it from a water-loving semiconductor into a brittle resistor. Dehydrated melanin amplifies stray DC currents from your phone's RF microwaves, electrocuting the anterior pituitary and gonads like a bad wiring job. Your jewels in the pocket? Zapped daily, dehydrating cells, spiking NaCl, and spreading electrical chaos where it shouldn't, straight to the mitochondrial cholesterol transporters.
Under ALAN, POMC flips from protector to tyrant. It bosses the cytochrome P450scc reaction, but without 380 nm sunlight to oxidize hemoglobin properly, cholesterol piles up undelivered. Mitochondria starve for substrate, cristae misalign under warped EMFs, and UPE signatures flicker like a dying bulb, low coherence, high noise, per Shannon's rules. Result?
Steroidogenesis grinds to a halt. Males lose testosterone at record rates (down 1% yearly since the '80s, per endocrine data), females watch estrogen and progesterone crater, and cortisol surges unchecked, frying adrenals. All your hormone panels?
Garbage light in, garbage hormones out, light controls this mitochondrial bottleneck MKULTRA mapped and weaponized.
Why screens over paper?
Why Obama and Biden's incandescent bulb bans? It's no accident. Society is easier to control without alpha males. Books under firelight preserved the optical circuit; blue-lit screens short it. The ionosphere's RF blanket dehydrates you globally, echoing the GOE's oxygen flood but with silicon instead of cyanobacteria. DARPA and FDA know: centralized MDs push Big Pharma TRT, but my tribe rebuilds the network—sun-gaze at dawn, ground to earth, ditch the blue devil.
Humanity's young bucks aren't broken; they're optically orphaned. Reclaim the 380 nm key, restore NO's whisper to POMC, flood mitochondria with cholesterol via real light, and watch testosterone roar back. The GOE taught us adaptation; MKULTRA's sequel demands revolution.The implications? This is the Danny Jones podcast on steroids, your low T isn't lifestyle; it's light warfare. Tune your mito network, or stay a lemming.
Retards like @axhoff never did their due diligence. They just post their ignorance because they are arrogant because they never put the PoW into the science.
2. Proof of science? PoW? See the top line.
3. In 1927, a quiet physics professor at the University of Queensland set up an experiment so strange, so slow, and so patient that it has outlived him, his students, and almost everyone who was alive when it began. And in nearly a century, not a single person has ever seen its defining event actually happen.
Thomas Parnell wanted to challenge his students’ assumptions about the physical world. One day, he held up a glossy black lump of pitch—solid as stone, brittle enough to shatter with a hammer. It looked completely immovable.
“This,” he told them, “is a liquid.”
When they laughed, he decided to show them.
Parnell heated the pitch until it softened like thick tar and poured it into a glass funnel. Then he waited three years for it to settle. In 1930, he cut the sealed stem and stepped back. Gravity would do the rest.
Eight years passed before the first drop finally fell in 1938. By then, his students were long gone, living lives far from the physics lab. The second drop fell in 1947—after a world war. The third in 1954. The fourth in 1962. Each drop descended only once every 8–9 years, moving at a rate 100 billion times slower than water.
But the strangest truth of all?
No one ever witnessed a drop fall. Not once. Not ever.
Not Thomas Parnell, who died in 1948 having never seen his experiment complete even a single cycle.
Not his successor, Professor John Mainstone, who took over in 1961. Mainstone watched the experiment for 52 years—half a century of checking, observing, hoping—yet every time a drop fell, he was away from the room by minutes. He missed one drop because he went to get coffee.
By the 2000s, technology was on their side. A camera was installed. Finally—finally—humanity would catch a drop in real time.
Except the camera angle was blocked.
The next drop? The footage corrupted.
It was as if the universe was playing a cosmic prank.
Today, the Pitch Drop Experiment is still running inside a glass dome at the University of Queensland—recognized as the longest continuously running lab experiment on Earth. A 24/7 livestream watches over it. Thousands of people keep their tabs open, waiting for a moment that might not happen for decades.
The tenth drop is forming now. Slowly. Patiently. Inevitably.
Here’s what Professor Parnell understood nearly a century ago:
Just because you can’t see progress doesn’t mean it isn’t happening.
Pitch flows. Mountains move. Continents drift millimeters a year. Coral reefs grow slowly, rings forming unseen. Blue light makes you gay and infertile. The most powerful forces in nature are almost invisible in real time. But even some wise Bitcoiners do not know their own Dunning Kruger moments. Be aware of this.
In decentralized medicine we look at your heteroplasmy ration for each organ.
Here is a sample I hand out to every client after their first private visit to me in El Salvador.
Aging is not one number. Each organ tells its own story about how much polarized and unpolarized light the owner of the organ has allowed.
2. Variation in Heteroplasmy Changes: Wallace enters my clinic exam room
Heteroplasmy (mixed wild-type/mutant mtDNA) disrupts the uniform 30 MV/m field, as mutants impair ETC (e.g., complex I/IV), causing charge mosaics that some see as a bioenergetic "interference" driving disease and evolution.
3. This idea directly ties to matrix geometry: heteroplasmic mitochondria lose e/g/k synchrony, widening V-angles → fragmented cristae → failed IMJs → network-wide charge instability. As a result the matrix emits more biophotons = more diseases of aging.
The main risks related to stereoisomers arise if a supplement contains an incorrect or mixed (racemic) form of a chiral compound:
Different Biological Effects: One stereoisomer may be active and beneficial, while the other may be inactive or even harmful. For example, the body primarily uses L-amino acids, and D-forms are often less bioavailable or utilized differently.
Toxicity: In the pharmaceutical world, the wrong enantiomer has, in some historical cases, shown different toxicity profiles, including teratogenicity or organ-specific harm.
For example:
The thalidomide tragedy of the late 1950s and early 1960s. This historical case points out what I am referring to in the peptide world or amino acid world of supplements. You never hear the food guru or peptide gurus tell you about the history of this risk so here you go.
Thalidomide was sold as a racemic mixture (containing equal parts of two mirror-image molecules, or enantiomers) and marketed as a safe sedative and an effective treatment for morning sickness in pregnant women. The different enantiomers had drastically different effects:
The (R)-enantiomer was the effective sedative with the desired therapeutic effect.
The (S)-enantiomer was a potent teratogen, meaning it caused severe birth defects in developing embryos, particularly affecting limb development (phocomelia), as well as eye, ear, heart, and internal organ development.
An estimated 10,000 to 20,000 infants in 46 countries were affected by these deformities. Many believe as I do these numbers are way under reported.
Crucially, even if the "safe" (R)-enantiomer had been administered alone, it would have been ineffective in preventing the harm because the human body's metabolic processes convert (R)-thalidomide into the toxic (S)-enantiomer, and vice versa, in a process called chiral inversion.
This disaster was a turning point in pharmaceutical regulation, leading to much stricter drug testing protocols and an increased understanding and focus on the importance of stereochemistry in drug development and safety testing. This was never applied to the peptide markets FYI. You have to TRUST that the lab or pharmacy does these tests.
2. More to worry about? Some peptide users in my client have developed amyloid changes. What did I tell them about continued use?
You might create a neurodegenerative disorder in your brain. Why?
Amyloid Beta (Aβ) peptides: In vivo, Aβ peptides, linked to Alzheimer's, can be found with D-amino acids (specifically Asp and Ser residues), indicating that a natural inversion process occurs, which affects their aggregation properties. This is an example of chiral inversion. This kind of freaked them out. When they questioned the lab/pharmacy and longevity docs who gave them this stuff communication completely shut down.
Decentralized medicine aims to educate not induce fear.
3. Why did I stop using NSAIDs in my patients around 2000? I read about homochirality and where it comes from. The physics of the cosmos.
Non-Steroidal Anti-Inflammatory Drugs (NSAIDs): While not peptides, a prominent example in pharmaceuticals (like ibuprofen) involves chiral inversion. The inactive (R)-enantiomer is metabolically converted into the active (S)-enantiomer by hepatic enzymes in the body, showcasing a clear biological pathway for inversion in a non-peptide context.
Tissue polarization by artificial light turn the matrix of mitochondria into a deuterium-gated racemization factory, turning mitochondrial proteins into mirror-image versions that:
a. reverse CISS spin filtering,
b. invert local PV asymmetry,
c. emit optically “backwards” UPEs that neighboring healthy cells can no longer read correctly,
d. and render affected cells invisible to immune surveillance by NK cells (D-peptides are non-self to TCRs that evolved under L-only rules).
2. COVID was more than a virus—it was a Parity Violation inversion, hijacking the iron at the center of life’s light engines. By disrupting heme, it dimmed the internal sun of billions. Homochirality allows for the precise folding and functionality of complex structures like mitochondrial matrix, proteins and RNA/DNA, which is essential for the high energy efficiency of aerobic life.
A "global change in homochirality" in a body was changed by the spike protein and was indeed catastrophic to the compliant, on an oxygen-dependent food web because ALL of that machinery of life relies entirely on this specific asymmetry.
3. Cytochrome C Oxidase is the key Parity Violation gatekeeper because Normal apoptosis is triggered when cytochrome C (a heme protein in the ETC) is released from the inter-membrane space into the cytosol.
Many do not know Cytochrome C Oxidase is exquisitely chiral (L-amino acids, PV-selected structure). Its release binds Apaf-1 in a stereospecific way to form the apoptosome → caspase cascade → orderly cell death.
Without an intact apoptosis SV 40 promotor would promote explosive turbo cancer formation in the compliant among many other PV diseases. It would mimic an extinction event to mirror the 5 we've already had.
In most cancers, the Bcl-2 family (anti-apoptotic) blocks cytochrome C release, or the apoptosome is mutated. No cytochrome C release = no chiral "death signal" = You are getting a turbo cancer.
Wondering if you'd be able to break down what happened after I took Venlafaxine (Effexor) a few years ago and if there's any specific things needed to be done to hopefully repair any damage.
After what I believe was a spontaneous CSF leak that happened one night and started all my chronic issues I was diagnosed with vestibular migraine around 3 months later.
Venlafaxine 75mg was indicated for this so I was on it for around 12 months (give or take the 3 months wean I did).
Within 3 weeks my emotions went numb, I lost my libido, erections and ability to pretty much feel love or any strong emotion. There was a very definite and obvious "change" but I believe I still had the ability to focus and enjoy hobbies etc.
After deciding to taper off, I would get brain zaps and all the other jazz that comes with it. After fully tapering, I was then introduced to anhedonia. Unable to feel or enjoy anything, unable to focus on anything for too long without getting the irritable and feeling like I need to do something else etc. Essentially feel there's been a permanent change since starting this.
This has improved slightly but not even close to where I'd like to be. Add all the daily brain fog, memory lapses etc and my brain is running on empty.
Does this need anything specific additional to the core light, water & magnetism?
Listening to this months webinar you mentioned accutane extending recovery from 6 months up to 5 years. This prompted me to ask this question and about my accutane use in the future as this is a huge jump in recovery time and shows how powerful these drugs are.
Thanks,
Ja$%^
3. Reasons Why Venlafaxine Could Cause Issues, Based on My Decentralized Thesis
My thesis posits that life's core "code" resides in conserved correlations of phase, spin, and topology, geometric invariants that maintain coherence beyond mere voltage gradients. Man-made electromagnetic (EM) pollution disrupts this coherence, leading to health risks like aging, cancer, and failed regeneration. Voltage is merely a "courier," while true memory and form emerge from photonic organization of spin and topological symmetry. Venlafaxine, as a synthetic molecule introduced into this already polluted EM environment, would act to exacerbate disruptions by interfering with biological EM phenomena. Below, I list hypothesized reasons grounded in its structure, spectra, pharmacology, and potential EM interactions. These are imaginative extensions based on my published framework, drawing from known drug effects and bio-EM principles (e.g., biophotons, ion flows, and field coherence), while acknowledging that direct studies on venlafaxine-EM-biology intersections are limited because BigHarma isn't going to harpon its own product with truthful decentralized science.