Remember the battle for the Nobel Prize between the discovery of HIV from Montagnier versus Robert Gallo in 1983?

Do you know that Robert Gallo began studying HIV in the jungles of the Congo in chimpanzees during the oral polio virus trials.

The first oral polio vaccine was aerosolized oral spray that caused cancers all over the mouth and sinus system. A bioweapons company did the work for DoD and Robert Gallo was on that team. Things you just do not know when you do not know your history. Did you know that Fauci support the Nobel Prize for his friend Gallo over Luke Montagnier?

Coincidence or might it be related to why Reagan hired Fauci in 1982?Image
2. How does it all fit into today's current events? forum.jackkruse.com/threads/ww1-th…Image
3. The first bioweapons lab on Magazine Street in NOLA and the work done at the US Public health hospital and Henry Clay Street in NOLA was transferred to the Tulane Primate Center in Covington Louisiana under the direction of Dr. Riopelle. When it became clear after the JFK killing in the mid 1960s that these simian viruses were behind many new human diseases like cancer and eventually HIV they were transferred to Fort Detrich as I laid out in my pod with RFK Jr. In the beginning Fort Detrich was an dual purpose base with the ARMY and CIA sharing thefacility and the bioweapons labs added to the mix as the science of Dr. Mary Stewart and Mary Sherman was developed by the CIA and industrial military complex.Image
4. The bioweapons lab in NOLA gave the military important bioweapon clues. Namely that nnEMF drive pathogenicity and it could be concentrated if many different viruses from competeing species were mixed before irridation. They were very deadly. These things were developed at Fort Detrich from 1963-68 in experiments called the Special virus leukemia Program.Image
5. This shows you where the military was in 1968. They were at a macro level dealing with data points in dead animals looking to see what was most effective in killing them. The miliatry was not the molecular level that one would need at furin cleavage sites to know the proper AMO physics to carry our mass death in living things. That science developed after Reagan hired Fauci in 1982.

When one plots the data of chronic diseases to when Fauci entered the industrial military health complex the data points do not lie. They tell a story that shows you it it not a story about food. It is a story of AMO physics and light to ruin mtDNA biology.Image
6. The most interesting finding from this Fort Detrich program was that the industrial military program was not looking to cure cancer, it was looking to make it more lethal. They found using animals closest to the human genome were the most deadly to humans. And then they amplified the effect through the early Nixon administration. @Kevin_McKernan The pathway to policy was clear. A new bioweapon policy was developed around vaccines using gene products needed to be developed by the military. This is where the ideas were born.Image
7. This paper really shows the origin of HIV. When the industrial military complex decided to mix the serum or primates and human serum togther and monitor the effects some very interesting findings started to show up in the literature early in Nixon's administration. This was 2 years before Nixon and Alton Ochsner launched the "War on Cancer" policy. That policy was designed to create a pile of money for covert bioweapon development. This money was laundered from the NCI to the military to continue on the pathway that General Groves began with Ochsner in NOLA during the Cutter Incident.Image
8. In 1970 they moved into the molecular medicine to see where the cancers can be recombined with across species. These are the genesis of gain of function studies done on US soil. This was legal before the 2001 Patriot Act. Now it is illegal and carries the penalty of death by Treason.Image
9. The last tweet shows you how viral chimera's were first built. You need to know that scientific accountability under our Constitution has not changed much since WW2. It rests with the Executive branch and this is why Gen. Groves capture this branch first in his silent coup on America by his shadow government. Why is this slide important. You'll notice the myriad of boxes who have to perform oversight for science and scientific misdeeds.

Groves had a lot to do with setting this system up because it gave the government scientific denialble plausibility in cases of misdeeds. I explained this to @nayibbukele when we met about the Constittional Amendment for his country. I told him RFK Jrs plan would not stop the problem with a Benjamin Rush like Amendment added to the ddcument because the industrial military complex knew this was the DOCUMENT's main weakness and they could exploit it using chronic disease management.Image
10. The next slide should give you chills. In 1969 they told Congress exactly what they were up to in viral chimera building and why they were doing it. Congress had ZERO issues with it and they allowed this via the oversight process. This was FUNDAMENTALLY why I disagreed with Bobby during the Tetragrammaton podcast with Rick on how to handle the chronic disease epidemic at its source.

We need a Constitutional Amendment to stop this freight train of the Deep State actors. This is when the military began to ensnare and capture the legistaltive branch of government. @KONCRETEImage
11. The industrial miliatry complex knew exactly what they were doing and Congress and Nixon helped them. If you listened to what I said about Nixon and what Bobby said about Nixon you'll notice we differed on our opinions of his legacy. This Act to Congress explicitly said that the military was now capable of making a bioweapon that would be immune to human immunity.Image
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12. For the non believers that your own government did this, this is the entire logic chart they used in the annual report of the project from 1972 when the War on Cancer was used as a psy-ops on America. Image
13. Fort Detrich was where mammalian viral pathogens were mixed in lab test tubes accross multiple species like cards in a casino deck to try to find the nastiest disease the miliatry could use to kill effectively. The slide below shows you the basic of how the system was developed by your own government.Image
14. So when someone asks you where disease really begin........and you answer food. You're an idiot because you have no idea about the history of how this process began with the Manhattan Project in the 1930s. Image
15. Once they created a virus that could collapse the enture immune system, they decided to find out how to alter immunity so that diseases could come on faster. Here was a paper I was assigned to read as a neurosurgery resident to understand the biology of the fast growing cancer called GBM in humans. Most autoimmune conditions are related to these mechanisms. Many cancers are. Many other chronic disease epidemic diseases are also linked to neuroimmune defects.Image
16. Why was Peter Duesberg an HIV denier. If you read the literature as I did, you'd know why. He knew where it came from. This is the same story we just saw with COVID that happened 40 years ago in HIV. Image
17. Deusberg knew what many of us knew that simian virus was grafted onto the human system and the vector was the VISNA platform. The result was the HIV "1983 discovery" It was no discovery at all. Any financial forensic journalist could perform a details accounting to find out where the money came from and went to, to figure out this "medical enigma"Image
18. This is the patent to making the monster Hepatitis B vaccine that all physicians had to take. Note the highlighted area. You now see 20 yrs after the list of simian viruses the military was using they were now producing vaccines with the science as a delivery mechanism. Now you can see why there was a need for Fauci 7 years later and the vaccine law in 1986 when the techniques moved from the DoD to BigHarma partners.Image
19. That Hepatitis patent was used by Merck in their Heptavax trial in 1978. That trial was the basis of why every healthcare professional and soldier had to take this jab. So I know my history and I know what the government is capable of. It is time some of you get your heads out of your ass and know it as well.Image
20. What was in the COVID jabs? Simian virus 40 promotor. Image
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More from @DrJackKruse

Apr 22
People, like the NYP are blaming this on climate change but they are missing the bigger point in the slide. for 540 my the oceans have been linked to the dynamo via oxygen. Everyone forgets it was the oceans where the GOE's oxygen came from not the tectonic plates. I believe this is another way government are trying hide the dynamo weakening to this story.

The at-risk current in question is the Atlantic Meridional Overturning Circulation, or AMOC, a “conveyor belt of the ocean” that circulates warm water toward the ocean surface from the tropics to the Northern Hemisphere.

NY Post:  nypost.com/2026/04/22/sci…

This is the "Geologic Sleight of Hand" currently being played out in science and the press. By framing the AMOC (Atlantic Meridional Overturning Circulation) collapse solely as a "Climate Change" event, centralized science is masking the Magnetic Stall of the planetary engine.

The Science Advances paper (June 2025 below) provides the evidence from my thesis: the dynamo and the oxygen cycle are a single, coupled Z-axis system.

1. The AMOC: The Ocean’s "Right Vagus"

The AMOC is not just a "conveyor belt"; it is the Planetary Vagal Exhaust.

The Vortex Function: The AMOC is a density-driven vortex that fractionates the ocean's "water table." It pulls warm, high-dielectric water north and "sinks" cold, nutrient-rich water.

The Magnetic Link: If the Universal Stator (the dynamo) weakens, the Lorentz force acting on the ionic sea water (the "Salinity" factor) decreases. The "pinning" of the ocean's vortex fails.

The Stall: The AMOC isn't "slowing down" because of melting ice alone; it is losing its Magnetic Torque. When the dynamo goes weak (as in the SAA/Neoproterozoic), the Z-axis vortex of the ocean "stalls," leading to the rapid de-oxygenation and Isotopic Stagnation we see in the "climate" data.

2. The GOE and the "Liquid Dynamo"

Oxygen didn't come from the tectonic plates; it came from the Oceans via the Magnetic Photolysis of Water.

The 540 MY Slide: The slide confirms that as the dynamo strength grew since the Cambrian, oxygen levels rose. This is because a strong magnetic field allows Melanin-like pigments (the early cyanobacteria) to split water without being "poisoned" by the Kinetic Isotope Effect (KIE).  People have forgotten that cyanobacteria made the oxygen in the GOE but cyanobacteria love to grow in high deuterium water and that is why cyanbacteria can be so toxic to humans.  This is a reminder that in the biggest magnetic decline event on Earth was during theNeoproterozoic era,  right before the Cambrian explosion. At the Cambrian is when oxygen yoked to the dynamo because the dynamo de-fragged itself by hardening its inner core to allow the dynamo to improve its own vortex and viscosity at the CMB barrier.

Today’s Inverse: We are now in the Reverse-Cambrian situation and everyone is calling this climate change when it is a MAGNETIC CHANGE.  It is a loss of flux in the SAA and Atlantic ocean. As the dynamo weakens, the ocean’s capacity to "filter" deuterium and "release" oxygen collapses. The AMOC failure is the "Isotopic Backflow" of the planet.

3. The "Climate Change" Mask

By blaming "CO2/Climate," the government avoids admitting that the Planetary Shield is fraying.

The Narrative: "Climate Change" is something they can "tax" or "manage" with software (policy).

The Reality: Magnetic Declination and the SAA split are "hardware" failures that imply the 160THz signal of the entire planet is shifting. You can't "fix" a dynamo stall with a carbon tax.

The Oxygen Drop: The drop in oxygen is the "Optical Blindness" of the Earth. It’s the sign that the Magnetic Pin for life is being pulled.  This is why Austrlia has a massive melanoma expeience.  They sit in an ocean that is even more effected and this alters the hydrology cycle of this continent.  When oxygen drops melanin is DEGRADED.  That is why they get melanoma. It is not the sun. It is a loss of the magnetic Stator

4. The SAA is the Atlantic Ocean's Giant "Red Spot"

The AMOC is situated directly in the path of the South Atlantic Anomaly.  It seems no one can see that data staring them right in their face.

The Flashover: As the SAA expands, it provides a "Magnetic Ground Fault" for the AMOC. It disrupts the dielectric constant of the seawater, increasing its "viscosity" (metaphorically) and making it harder for the vortex to "sink" at the poles.

The Result: A stagnant ocean leads to a stagnant atmosphere, which leads to Deuterated Rain (Isotopic Insufflation) falling on the "Y-axis" of all life.

5. My decentralized Synthesis: The "Hydraulic" Collapse

The AMOC collapse is the "Empty Sella Syndrome" of the Earth. It is the hydraulic "squish" of the planetary water table because the Z-axis torque has failed.

Centralized Failure: They are looking at the "fever" (surface temperature) but ignoring the "Magnetic Sepsis" (the loss of dynamo power).

The "Climate Crisis" is a Magnetic Stator Crisis. The AMOC is the first symptom like a "Nerve Root Sleeve, cyst, or tumor" is for deuterium in the CSF around a nerve or a symptom of the planet to show the Isotopic Sludge is the real culprit.Image
2. Why are mosquitoes now in Iceland? They are following the magnetic field they can sense because the one in the South Atlantic is gone. Mosquiotos are arthopods that navigate by the radical pair mechanism. Another sign that it is not climate change.

It is magnetic field loss that links all these " unusual events." invaltec.com/magnemax/Scrip…
3. How does this mechanism work? elifesciences.org/articles/44179
Read 7 tweets
Apr 19
All he needs it a bilateral VNS to de-frag him. The centralized Canadian docs you hired are clueless. I do a the left one the old fashion way and then I'd use the right ear to VNS the right one due to his symptoms. If cognition is impaired the VNS needs to go on left. I’ve revealed how evolution used the mechanical throb of the Aortic Arch as a high-fidelity "de-fragmentation" tool for the left hemisphere’s cognitive centers.

If he has spatial awareness and emotional lability then it should go on the right side. Why? The right vagus travels behind the esophagus and bronchus, coupling with Breathing Motions.

The Right-Brain Connection: The right brain is more tied to spatial awareness and emotional "GPS." The aural VNS can go on the opposite side avoiding issues with bilateral RLN issues with dual VNS.

Akathisia, which is a state of severe motor restlessness, is traditionally linked to the blockade of Dopamine D2 receptors in the striatum.

The Striatum requires high-velocity dopaminergic firing to maintain motor "quietude" in the motor outflow.

The Viscosity Trap: As the ventricular deuterium leaks into the striatal tissue, it increases the viscosity of the interstitial fluid.

D2 Receptor Failure: The "stiff" 𝐶−𝐷
bonds due to the KIE of Deuterium in the receptor proteins slow down the conformational changes required for dopamine binding. This creates a "stutter" in the feedback loop between the striatum and the cortex.

The Sensation: Akathisia is the conscious perception of this dielectric "friction." The person feels they must move to "shake off" the internal stagnation, but because the source is the "heavy" water in the lateral ventricles, no amount of movement can fix the signal.

Peterson disease is just like SANS in astronauts. This is why SANS (Spaceflight Associated Neuro-ocular Syndrome) and neurological "glitches" are so prevalent in astronauts crossing the SAA.
This blog covers it all. Hand to you centralized moron MDs and get your Dad better. This story is boring me with how bad you guys have played your hand. patreon.com/posts/decentra…
2. Why are the left and right Vagus nerves asymmetric? Because life is and so are your hemispheres.
3. Peterson's Answer is the the following. Fire your doctors and family and get somebody on your team who understands how to improve HRV from a Magentic stall.

Doppler flows and thermograms of the great vessels would show you have lost the dielectric constant in the water in your circulatory system.

If the anesthesiologists or allopathic MDs understood the Z-axis of the human GPS system, they would see JP case is like Micheal Jackson's death. Using exogenous Propofol to sleep was a "Magnetic Darkness" event aka why Micheal Jackson died and the benzodiazepine abuse of Jordan Peterson behind his recent development of drug induced Akathisia are the same.

This is the biophysical post-mortem of modern allopathic failure. I’ve just linked for my savages that the high-profile "anomalies" of Michael Jackson and Jordan Peterson to a singular event: the Z-axis Magnetic Stall of the heart vortexing blood.

When MDs prescribe these drugs, they think they are "calming the brain." They don't realize they are quenching the biophoton field and creating an "Optical Blindness" that the body interprets as a death-signal. That is what I had planned on telling his family but they chose a diet solution of the real answer.

Michael Jackson: The Propofol "Darkness"

Propofol is a potent suppressor of Heart Rate Variability (HRV) and the Z-axis GPS signal. Look it up.

The Blackout: By flattening the HRV "vortex," Propofol stops the centripetal force required to eject deuterium from the mitochondria.

The SAA Effect: Using Propofol daily is like forcing the brain to live in the center of the South Atlantic Anomaly 24/7.

The "Death" Signal: Without the chaotic Z-axis signal to "pin" the protons, the 160THz light in the brainstem (the "Universal Stator") went out. Jackson didn't just stop breathing; his Topological Insulator collapsed because he had no "magnetic pressure" left to maintain the CSF lattice in his brain. Game Set match.

Peterson will go down the same way if they do not wake up.
Read 7 tweets
Apr 18
Chromothripsis is typically triggered by errors during mitosis, such as the formation of a micronucleus. Recent research suggests that deuterium overload can play a role in this "shattering" process:

Kinetic Isotope Effect (KIE): Deuterium (D) forms bonds that are 8-10 times stronger and harder to break than normal hydrogen (H).

Mitotic Disruption: This mass difference can cause "stutters" in the molecular motors (like Fo-ATPase pumps) that manage energy and cell division. When these motors fail, chromosomes are more likely to lag behind or mis-segregate into micronuclei, leading directly to the shattering seen in chromothripsis. Kev is right chromothripsis is down stream deuterium biology because the KIE controls clock speeds and a slow clock causes cancer because atomic mass (D+) is weighing down the DNA and it cannot be read on time.

The base chain of life, DNA is designed to be undeuterated to get perfect signal and eliminate the noise cause by deuteration.
2. What does this slide really mean? The slide highlights a massive biophysical paradox that mainstream medicine largely ignores: Deuterium is the most concentrated "vital element" in human serum, yet it is functionally excluded from the mitochondria. Rockefeller medicine teaches MDs to focus on glucose and K+ but deuterium has 10X the concentration in blood where no RBC have mitochondria because of this partitioning.

When a cell has mitochondria, our human Langrangian seeks to keep it from the matrix at all costs. When it gets this is when cancer becomes a real possibility.

H+ breaks time symmetry in mammals so we can live in a highly dissipative state, while D+ invites symmetry and this leads to disease and eventual rigor mortis. Life is not meant to be symmetric or at equilibrium. That is why biochemists are morons and why biophysics shows the equation of Everything. H+ and D+ are handled asymmetrically in the eukaryotic kingdom.Image
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3. Methylation and "Heavy" DNA:

As my thesis notes, methyl groups (𝐶𝐻3) are central to DNA regulation. When these groups are deuterated (CD3)

Gene Expression: Research indicates that a higher D/H ratio in the cell acts as a "trigger" for oncogenes like c-Myc and RAS while suppressing tumor suppressors like TP53.

Methylation Patterns: Altered D/H ratios can disrupt the tight regulation of DNA methyltransferases, potentially leading to the global hypomethylation and site-specific hypermethylation that characterize cancer. They also alter the UPE signal need to progress past mitosis ibn the cell cycle.
Read 6 tweets
Apr 16
This is a perfect example of the "Centralized Blind Spot."

Mainstream centralized medicine is celebrating the "technology" of the skin-to-neuron conversion, while completely missing the Biophysical Diagnostic staring them in the face: Why was the skin still "functional" while the brain was a "dead zone"?

In my decentralzied framework, this confirms the Ventricular Stall theory of neurodegeneration.
2. The Brain as the "Isotopic Sink"
The "Centralized Nonsense" assumes Parkinson's is just a "lack of dopamine." You see it as a failure of the 4th Ventricle "Centrifuge."
The Brain's Burden: As the highest-density deuterium environment (150ppm blood supply + massive cardiac output), the brain must spin its CSF vortex at high RPMs to vent the "Heavy" isotopes.
The Brain Stall: Parkinson's occurs when the brain's magnetic "stator" (decimated by nnEMF/Blue Light/SAA) can no longer clear the CD3 (Deuterated Methyl groups). The brain lattice becomes "Heavy," the dopamine-producing neurons "short circuit" under the UPE load, and the system locks up.
3. The Skin: The "Low-Flux" Survivor
Why did the skin cells work?
Lower Isotopic Pressure: The skin is a peripheral tissue. It doesn't have the 20% cardiac output/high-flux requirement of the brain. It is "less heavy" because it isn't the primary recipient of the body's isotopic waste.

The Transplant Logic: By taking skin cells (which still have a functional "archean" memory and lower isotopic grout) and placing them in the brain, they have essentially "imported" fresh, light-water machinery into a heavy-water swamp.

The 12-Month Clock: The scientists are amazed the cells are alive after a year. In my model, the clock is ticking.

Unless they fix the CSF Vortex Stall, those new cells will eventually "deuterate" and stall just like the original one. this is why neuralink is being developed to de lattice astronauts after two yrs of space travel where NASA will have to stop the IMM at cytochrome one just like satellite owners have to shut down their satelites as they fly through to the SAA to avoid lattice lock. This is why Oocytes stay healthy in the human ovary once formed. The body does not expose the germ line to deuteration when it is unnecessary.Image
Read 5 tweets
Apr 16
This "discovery" is a classic example of mainstream science stumbling into Robert O. Becker’s territory and mislabeling the mechanism because they lack the biophysical "Rosetta Stone."

When Wong claims it’s just "pH changes" and "evolving gases," he is looking at the exhaust pipe and thinking he’s found the engine.

The decentrlaized medicine assessment is: this isn't just electrochemistry; it’s the re-liquification of the collagen lattice via the DC current of injury.

In Fourth Turnings centralized scientists try to steal ideas like bankers steal your time via fiat banker games.Image
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2. The Becker Connection: The DC Stator
In the 1960s, Becker proved that a small DC current (nano-amperes) is the signal for morphogenetic repair.

The Error: Hill and Wong "accidentally" hit the sweet spot, the exact low-amperage current that signals the tissue to enter a "plastic" state.

The Reality: They aren't just "softening clay." They are using electrons to disrupt the Deuterium-heavy hydrogen bonds that make aging or damaged cartilage/corneas stiff. By lowering the resistance, they allow the collagen to "unfurl" and reset its dielectric state.

This is not new this is what Archea were doing 3 billion years ago in oceans with no oxygen.Image
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3. The "Eukaryotic Lagrangian" Reset
I mentioned the Archean aspects. This is profound insights to morons in centralized fiat science. By applying that specific current, they are temporarily bypassing the modern "oxidative" noise and forcing the tissue back into a Pre-Cambrian regenerative mode.

Cartilage as a Semiconductor: Cartilage and the cornea are collagenous liquid crystals. They are designed to hold a charge.

The "Mistake": By using "too little current," they avoided cooking the tissue (thermal/Rockefeller approach) and instead engaged the Electronic/Biophysicalapproach. They accidentally tuned into the resonant frequency of the water lattice.Image
Read 5 tweets
Apr 16
For decades, the search for the biological roots of severe depression has largely focused on looking for physical changes in the brain's shape or size. It has never once looked at how the sun changes the viscosity of water that makes up the CSF and now that is slowly changing. Thermograpghy shows when blood is lattice lacked and it can show when CSF is lattice locked and stops flowing well in a vortex. This happens when its dielectric property changes from 78 to 160 in sunlight. This is why depression is always linked to low levels of sunlight and grounding to improve magnetic inclination of melanin in the brain. People forget melanin and oxygen are both paramagnetic. This is why they links exist.

However, major new research is fundamentally changing how we view the condition, revealing that the true key lies in how the brain operates in real-time using sun and grounding. The centralized ​scientists have not got it all together yet but they are bginning to utilize tools that will get them to my level of biophysical understanding.

Advanced imaging techniques have discovered that depression is strongly characterized by localized drops in cerebral blood flow. This reduced blood flow creates a domino effect, preventing neighboring clusters of brain cells from communicating and synchronizing properly.

Essentially, these specific regions are not receiving the optimal energy and oxygen required to maintain healthy neural connections. ​This discovery is a significant leap forward for mental health science.

By focusing on active blood flow and neural synchronization rather than physical structural scans, researchers have found a highly precise biological indicator that directly mirrors the intensity of a person's symptoms.

This deeper understanding paves the way for a new era of targeted, objective measurements and treatments focused on restoring healthy brain activity.

Journal Cite: Kochunov P, Adhikari BM, Keator D, et al. Functional vs Structural Cortical Deficit Pattern Biomarkers for Major Depressive Disorder. JAMA Psychiatry. 2025;82(6):582–590. DOI: 10.1001/jamapsychiatry.2025.0192Image
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2. This JAMA Psychiatry study from June 2025 is the "accidental" confirmation of my thesis. While centralized science celebrates finding a "functional biomarker" for depression, they are actually just measuring the Isotopic Stalling of the brain's particle accelerator.
By focusing on "localized drops in cerebral blood flow," Kochunov et al. have finally stumbled upon the Viscosity Map of the depressed brain.

1. The "Heavy" Sludge: Viscosity is the Variable

My slides makes the connection clear: Blood and CSF are thixotropic. Their flow is entirely dependent on the Zeta Potential and the Melanin-Water battery.
The Discovery: The "localized drops in blood flow" are not caused by "clogged" vessels, but by increased viscosity due to Deuterium loading (2H).
The Physics: Deuterium is twice as heavy as Protium and creates stronger hydrogen bonds. This makes the CSF and blood "thicker." In a region of the brain where the magnetic dynamo's coupling is weak (like the SAA or high-declination Azores), the 2H isn't fractionated out by melanin.
The Result: The blood literally slows down because it is too "heavy" to be moved by the heart’s vortex pressure at the normal 9,000 RPM ATPase rate.
3. Neural Synchronization: The Phase-Lock Failure

The study notes that reduced flow prevents brain cells from "synchronizing properly."

My Lagrangian Rebuttal: Synchronization is Phase-Locking. As you’ve established, the brain is a coupled oscillator slaved to the magnetic dynamo.

The Magnetic Wrench: When 2H increases viscosity, it "detunes" the elastin-melanin highway. The "mechanical jitter" (Piezo1/NOX2) creates electromagnetic noise that breaks the Chiral Handshake of melanin and oxygen to the dynamo.

Depression as "Stall": Depression isn't an "emotional" state; it is the Ohmic dissipation (heat) of a brain that has lost its Quantum Coherence. The neurons aren't communicating because they are drowning in a "symmetric dead state" of heavy water.Image
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Read 6 tweets

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