@matthew_labosco Trying to counter or resist those behaviors won't work. They are the symptoms, the results of using a system you can't see. Until you do, you're just spinning your wheels.
@ErwanLeCorre The body, the imagined home of the “I”, is subject to destruction over time, and the mind that stakes its claim to life on that identity lives in constant anxiety about its demise.
Youre neither the body, nor the “l”. Holding your breath won't lead you to that recognition.
@ErwanLeCorre Entheogens can take you to the source of your imagined life, the “I” you believe yourself to be, and open the view beyond that identification.
Robert Becker discovered a semi-conductor based electric system in the body.
Semi-conductors have a crystal lattice structure that allows their electrical conductivity to be controlled.
Melanin is the body's semi-conductor.
More sunlight = better electrical flow. ☀️⚡️
What if food isn't your body's energy source?
Melanin uses light to split water and generate electrical energy that powers your cells.
The light you’re exposed to matters ☀️
🚨 This is INSANE.
CANCER has been Cured via something found in Japanese forests.
• Literally ERADICATED TUMORS IN A SINGLE DOSE
• Head to Head against chemo & immuno — worked Way Better
• No bad side effects
• Prevented Recurrence: the cancer COULD NOT be brought back
All this was possible via a single bacterium isolated from the intestines of Japanese tree frogs - Ewingella americana. 🐸
➡️ When a single dose of the E. americana was injected into the veins of mice bearing colorectal cancer, the tumors were 100% Rapidly, Completely eliminated.
➡️ No side effects (except mild necessary inflammation, gone w/in 72 hrs). No signs of long-term toxicity (multi-month observation period).
➡️ It also induced immune memory against rechallenge (prevented cancer from coming back).
➡️ And importantly: Zero colonization in normal organs + GONE from the body w/in 24 hours.
➡️ It's Highly likely these results will translate well to humans & to other (especially solid tumor) cancer types.
I pay attention to cancer studies (have for decades) and these are actually an INSANE results.
✅ Why E. americana is the perfect CANCER KILLING MACHINE:
• E. americana thrives in the same (low oxygen, immunosuppressive) environment tumors thrive. And proteins + metabolic byproducts that cancer cells produce actually support the growth of E. americana, right there near the tumors.
• Tumor blood vessels are poorly structured, very permeable/leaky. Because of this, E. americana can easily exit the bloodstream and enter the tumor tissue.
IN OTHER WORDS: when this bacterium is injected, a perfect symphony transpires where it goes DIRECTLY to tumors & eliminates them — while leaving normal cells & organs alone. 😯
✅ HOW IT WORKS:
E. americana eliminates cancer via 2 mechanisms:
• Directly damages cancer cells.
• Activates immune system — E. americana attracts T cells, B cells, and neutrophils to the tumor area (which then eliminate the cancer cells).
✅ WHY THIS IS LIKELY TO WORK IN HUMANS:
Curing cancer via bacteria has been tried before. Here's what we know.
⚫️ Efficacy results shown in mice usually DO translate to humans— ie. bacteria that accumulate in mice tumors usually do the same w/in a human body
⚫️ Toxicity results shown in mice also show up similarly in humans
⚫️ There has Never been a mice study showing results this good OR w/o toxicity (the other ones showed a lot of toxicity & even death in the mice)
⚫️ In other bacteria cancer studies: the bacteria DID accumulate in normal organs. This one does not.
⚫️ IMPORTANTLY: all other bacteria that have been tried thus far were bioengineered/GMO.
⚫️ E. americana is naturally occurring & far less likely to lead to bad side effects.
So anyway. Given these INSANENELY EFFECTIVE & safe results...they surely will FAST TRACK human trials on E. americana (perhaps on those who have nothing to lose and everything to gain) Right? ...Right?!
I doubt it. It'll probably be forever... IF they even let this get to the public.
They'll probably announce some new "miracle" genetic therapy instead, and try to pull all attention & resources toward that.
UNLESS we do something.
Be loud. Share this. Don't let this die down and be forgotten about.
This is one of the most promising "1 & done" type of cancer solutions I've ever seen.
But even if this does become mainstream, Natural Medicine & healthy living will still have it's place. This therapy does require an at least somewhat functioning immune system to work.
And know: there are ways to fix your body.
Please see my other posts on cancer reversal via high dose IP6 (Inositol Hexaphosphate), large amounts of vegetable juicing (carrots/greens especially), high doses of specific mushrooms (Mesima, certain types of Reishi), etc.
I've posted tons of studies & reversal reports (often stage 4).
Nature is amazing. Spread the word.
recorded a total and absolute BANGER with @DrJackKruse this morning, re: the coming magnetic pole flip, and the implications of magnetic declination on: health, despeciation, geopolitics, space travel, tech development and more. this is the most important podcast i’ve ever recorded. it’s up on spotify as well on Undoctrinate Yourself podcast.
https://t.co/GDrLiL3550
How does WiFi cause cancer? It causes hypermethylation with Deuterium. The slide explains the mechansim. My words are definitive on it because it is based on the laws of physics.
This "hexose image" from Boros and Somlyai is the "Isotopic Wiring Diagram" for the Metabolic Meltdown of a cell. In my decentralized framework, it represents the moment the Z-axis (The Heart) fails to provide the Magnetic Vortex necessary to fractionate the "Oncoisotope" Deuterium (D+). Here is how this biochemistry operates biophysically on DNA through the lens of the Heart’s Magnetic Vortex:
1. The Heart as the "Isotopic Centrifuge" The Magnetic Vortex in the ventricles is the physical driver of the J-vector (Angular Momentum). The Vortex Function: As blood pulses through the heart's helical chambers, it creates a centrifugal pressure gradient. Because D+ is twice as heavy as +, the vortex "spins" the heavy isotopes toward the vessel walls (The Exhaust), leaving a "Protium-Pure" stream for the high-resolution organs (The Brain and DNA). The Z-Axis Failure: In the cancer cell (image), the "STOP" signsindicate the Z-axis Vortex has stalled. The + is no longer being "pinched" out of the flow.
2. Biophysical Drag on the DNA Lattice When the heart's vortex fails to fractionate +, the "Heavy" atoms flood the G6PDH/NADPH pathway shown in the image. The Lobry de Bruyn "Stall": The image mentions Lobry de Bruyn transformations (isomerizations). In a "Protium-Pure" environment, these happen at the speed of light. But + acts as an Inertial Anchor. Its different magnetic moment and mass create a "Chiral Speed Bump." DNA Stability: The DNA is a 1D Lattice. To replicate or repair, it must "unfurl" with near-zero friction. If the G6PDH pathway is feeding the nucleus +-rich "Heavy" nucleotides, the DNA becomes "Inertially Massive." It cannot "vibrate" at the 40Hz Gamma truth. This is the biophysical definition of Genomic Instability.
3. The "Hypoxic" Mitochondria: A Lack of "Light" Water The image shows that Low Deuterium Metabolic Water production is defective. Metabolic Water (2 vs 2): The mitochondria are designed to produce "Light" water through fatty acid oxidation. This light water has a High Dielectric Constant ( > 78.5). The Dielectric Shield: This light water surrounds the DNA, acting as an "Optical Shield" for the UPE signaling (Ultra-weak Photon Emission). The Cancer Crash: When the heart's vortex stalls, the mitochondria become "Hypoxic" and start producing "Heavy" Metabolic Water (2H = D+).
This lowers the dielectric constant, "clouding" the Sphenoid Mirror and allowing the Fenton Fire to burn the DNA.
4. The "STOP" Sign: The Vagal Blockade The red "STOP" signs in the image are the Vagal Blockade at the molecular level. The Impedance Mismatch: Because the Exhaust Manifold (The Vagus) is welded shut, the D+ sludge cannot egress. It backs up from the mitochondria into the Pentose Phosphate Pathway. Energy vs. Time:
The cell reverts to the "Left Side" of my Lagrangian slide (below), which is the Bacterial/ATP model. It chooses "Energy" (Fermentation/Glycolysis/Warburg/Food) because it has lost the "Time" (The 4D Phase-Lock) required for Mitochondrial Respiration.
CITES
https://t.co/02bpIp4KDn
DMSO is a polar, aprotic solvent that has a profound affinity for water.
The Mechanism: When DMSO enters a "stiff" water lattice (dielectric 78), it disrupts the hydrogen-bond network of water.
The deuterium Fractionation: By breaking these bonds, DMSO "loosens" the grip that 150 ppm deuterium has on the water lattice. It effectively acts as a "chemical centrifuge,"helping to "un-weld" the isotopic deuterium silt from the cell membranes and mitochondrial intermembrane space.
https://t.co/SBbfD3imCs
DMSO is not chiral itself, but it acts as a Chiral Solvent Substitute that restores the Chiral Induced Spin Selectivity (CISS) in a "seized" lattice.
In my decentralized framework, it isn't just a "pore maker", it is a lattice breaker in things made from water with a low dielectric constant.
DMSO crosses the BBB effortlessly. This is why it is the ultimate" Decentralized Mechanic's Tool" for the 4th Ventricle Vortex.
LET ME FIX THIS TWEET WITH REAL SCIENCE: THE BIOPHYSICS OF LSD.
The case of the 97-year-old woman is the clinical proof that "Reincarnation is simply truths that survive everything." Her "Self" hadn't vanished; it was simply Isotopically Drowned in a high-inertia lattice.
1. The LSD-Deuterium Depletion Mechanism
LSD (20253) is a complex, chiral indole alkaloid that mimics what melanin does in human neuroectoderm. It chelates deuterium because of its unusual magnetic moment. Its structure allows it to act as a Symmetry Breaker (SU(2)) within the mitochondrial matrix.
LSD binds with high affinity to 5-HT2A receptors, which are densely packed in the Thalamic GPS and the Cerebral Cortex. This binding triggers a second-messenger cascade that upregulates BDNF. BDNF isn't just a "growth factor"; it is the signal to increase the capture cross-section of the mitochondrial antenna. It forces the TCA cycle to "spin" faster, using the Woodward Effect to centrifuge (Deuterium) out of the [Fe-S] clusters.
The Result: The "Ohmic resistance" drops. The "Twiddly Link Ball Bearings" (protons) can tunnel again. The 97-year-old woman regained awareness because the DC Polarity (Becker) flipped back to Frontal Negative. The "Vagal Blockade" is the primary reason Alzheimer’s patients enter a vegetative state, the Exhaust Manifold is welded shut with + sludge.
The Serotonin Link: The Vagus nerve is the primary highway for serotonin signaling between the gut and brain. By agonizing the 5-HT receptors, LSD acts as a "Drano" for the Vagus to gsain mixing in the pancreas with the 2L of Bicarb in the carbanic anhydrase system.
Pressure Equalization: It matches the Impedance of the Thalamus to the Pancreas/Bicarb exhaust. This allows the Cerebrospinal Fluid (CSF) to finally "dump the ballast" of accumulated deuterium into the gut for egress. This is why she emerge from her haze. It had nothing to do with BDNF new neurons. It was an opening the drain to slowed her consciousness.
The 97-year-old woman did not “grow new neurons.” She un-drowned the ones she already had by restoring the low-entropy, polarized DDW lattice Ling mapped and the Landauer-compliant proton tunneling the 2025 Nature Physics paper quantifies.
2. Chiral CISS mechanism: the quantum filter that re-opens fractionationChirality-Induced Spin Selectivity (CISS) is the missing quantum piece Ling never had. Chiral molecules (like LSD, melatonin, serotonin, and the amino acids in ferredoxin) act as spin filters for electrons and protons:
When a chiral molecule binds, it preferentially transmits electrons/protons of one spin orientation while blocking the opposite.
This spin-polarized current aligns proton wires in the structured DDW layers (dielectric constant of 160) and the [Fe-S] clusters.
Deuterium (spin-1 boson) is heavier and disrupts this spin coherence. CISS-enhanced binding (LSD → TrkB or serotonin pathways) restores the spin filter, ejects deuterium from the mitochondrial matrix, and re-establishes the coherent phase transition.
Influencers stop at biochemiscal knowledge. Savages go to the top levels of biophysics.
LSD (via direct TrkB binding + CISS spin filtering) acted as a chiral cardinal adsorbent that centrifuged deuterium out of the mitochondrial matrix, reopened the vagal exhaust, and restored the Spira Mirabilis at every stage, aqueduct, Luschka–CPA, and heart vortex. Centralized medicine will keep calling this “psychedelic plasticity” or “serotonin magic.” The thesis calls it reincarnation via isotopic re-fractionation.
The chiral CISS mechanism is the quantum filter that lets the heavy octave (deuterium) stay sequestered in blood while the light octave powers coherent UPE signaling and protein folding. Remove Alien Light, add coherent 432 Hz harmonics, restore sleep-driven Venturi flow, and the lattice re-forms. The body does not need new neurons from BDNF. It needs the deuterium bomb removed so the original ones can breathe again.
The system was never broken in this AD case. Her head was filled with deuterium she could not clear.
It is still obeying the same archaeal-derived harmonic centrifuge that navigated deuterium under the unshielded Archean Sun.
The 2023 Nature Neuroscience paper is the clinical Rosetta Stone.
Centralized training simply never learned to read the chiral spin filter, or the music of the spheres that keeps it tuned.
CITES
1. https://t.co/HnjBZodw4P
2. https://t.co/rwiMOWHiY4