Leo

[jack @jack]

we're launching BUZZ!

a new groupchat platform for teams of people and agents of all sizes, built to reduce our dependency on slack and github. model-agnostic, decentralized, self-sovereign, and open source. 🐝

https://t.co/8IaMVeTQNo

[Collectooor of dice 🎲☣️🪢 @hoardingsats]

Satoshi saying #Bitcoin should keep arbitrary data OUT #BIP110

[Dr. Jack Kruse Decentralized Medicine Maxi 🔆 @DrJackKruse]

Let me upgrade the tweet. From the hard laws of optical physics, the following three cellular components demonstrate the most extreme optical anisotropy in the human body:

1. The Myelin Sheath Superlattice (Extreme Form Birefringence)The Physics: Myelin is a highly ordered, alternating lipid-protein concentric wrap. Because its structural layers are smaller than the wavelength of visible light, it exhibits intense form birefringence.

The Blueprint: When wrapped tightly around axons, this anisotropic lipid matrix acts as an all-optical waveguide. It forces light to maintain a strict polarization axis, preventing the loss of coherent biophotonic signals as chaotic thermal noise.

2. The Collagen Triple Helix Matrix (Extreme Intrinsic Birefringence)The Physics: As the primary component of bones, tendons, fascia, and the cornea, collagen is composed of highly oriented, crystalline triple-helical protein rails. This geometry gives it a massive uniaxial positive birefringence.

The Blueprint: This extreme anisotropy allows the extracellular connective tissue grid to function as a macroscopic, solid-state liquid-crystal semiconductor network. It couples physical mechanical stress directly into electrical current via piezoelectric induction.

3. Retinal Photoreceptor Outer Segments (Extreme Dichroism)

The Physics: The outer disks of rods and cones, packed densely with the photopigments rhodopsin and iodopsin, are stacked like a series of parallel optical plates. They exhibit profound linear dichroism and birefringence, absorbing light with extreme dependency on the photon's electric field vector orientation.

The Blueprint: This extreme optical asymmetry forms the foundation of the retinal clock. It enables the eye to serve as an optical magnetic compass, directly transducing the polarization angles of ambient solar light and the planetary magnetosphere into clean, direct current (DC) homeostatic signals.

[Dr. Jack Kruse Decentralized Medicine Maxi 🔆 @DrJackKruse]

Boom. Physics> Pharma from 2017

[Leo @LeoVP37]

@JoshuaK__ @zaidkdahhaj @Mitopapi @Seasonal_Ryan @jack_schroder_ @ze_rusty @helios_brah Grounding sheets and💧

[Leo @LeoVP37]

@AmmousMD 😂😂😂😂😂

[Leo @LeoVP37]

@Torito1774 @ze_rusty 🤝

[Leo @LeoVP37]

@DrJackKruse

[Dr. Jack Kruse Decentralized Medicine Maxi 🔆 @DrJackKruse]

LOL. Nope. It is the melanin that chelates Ca2+ that is missing thst causes it. K2 is the answer when the dielectric is normal. Today, no one is. LOL. Influencers.

[Dr. Jack Kruse Decentralized Medicine Maxi 🔆 @DrJackKruse]

This is the "Chemical Warburg Shift" in its most devastating form. PSSD (Post-SSRI Sexual Dysfunction) is not a psychological "side effect"; it is a biophysical "hard drive wipe" of the body’s topological surfaces.

When you apply my framework to the PSSD story, the mechanism becomes clear: SSRIs are powerful deuterium-concentrators that collapse the dielectric constant of the nervous system.

1. The "Emotional Lobotomy" as a Dielectric DropYou’ve noted that music and love require "photonic proteins."The Coherent Wave: Love and the appreciation of music are high-frequency, coherent ferron waves moving through the K+)-stabilized water of the brain.

The SSRI "Sludge": Fluorinated drugs like many SSRIs (Prozac, Paxil, etc.) or those that disrupt the CYP450 enzymes interfere with the body's ability to fractionate deuterium.

The Result: The "inner sea" of the neuron becomes deuterated. The dielectric constant (E) drops from 160 back toward the bulk value of 78. In this low-E environment, the "Velocity of Life" (v = square root of {2gy) stalls. The ferrons cannot propagate, leading to the "numbness" of the clitoris and the "numbness" of the soul.

2. The Melanin-MITF Connection in PSSD
The genital numbness and loss of libido are direct evidence of a Melanin/Catecholamine backslide.Genital Topology: The genitals are the most highly innervated and "topologically active" surfaces of the body. They require massive amounts of dopamine and melanin-derived semiconductors to function.

The MITF Shutdown: SSRIs are known to interfere with the AMPAR receptors (as you noted with Lasix). This triggers the downregulation of MITF, the factory manager. The body stops producing the melanin and catecholamine "sparks" required for orgasm and empathy.

The Result: The system "defrags" into the toxic precursors (Tyrosine/PA). Without the "Right-ward" photonic flow, the clitoris becomes as biophysically "silent" as the back of an elbow.

3. Why it Persists: The Deuterium Trap

The most tragic part of PSSD is that it remains after the drug is stopped.

The "Static" Memo: Just like the ancient magnetic field "frozen" in the rocks of Hawaii, the Deuterium is frozen into the collagen and neural stroma.

The Collapse of the EZ: Once the SSRI collapses the Exclusion Zone (EZ) water, D+ floods the mitochondria. This "heavy" environment prevents the K+ from re-anchoring the water lattice. The cell is stuck in a permanent Warburg Shift because it no longer has the dielectric "torque" to kick the deuterium out.

4. Reconciling with the "Dynamo"

If Life is a wave generated by the Dynamo, an SSRI acts as a magnetic shield that decouples the person from Earth's field. They are "magnetically orphaned." This is why they can't feel music, they have lost the ability to "resonate" with the frequencies of the environment.

My Decentralized Summary: PSSD is "Topological Extinction." The drug causes a "chemical backslide" into a deuterated, low-oxygen, high-matter state. To "reboot" someone like this, you have to do more than stop the drug; you have to re-polarize the stroma using the "Cambrian" toolkit:

Deuterium-Depleted Water (to flush the "heavy" motors). UV-A and Red Light (to trigger MITF and re-establish the photonic flow).

Zero Declination Alignment (to provide the magnetic torque for the "Lagrangian" hand-off). I also use 3% saline IV using Lactated Ringers to activate the G3P shuttle.

[Dr. Jack Kruse Decentralized Medicine Maxi 🔆 @DrJackKruse]

Not one mention of water's dielectric constant or the magnetic polarity flip found by Becker in his work. This is bad science.

MT cannot function without water surrouding them or operating inside of them. When you change the dielectric constant at water that induces the unconscious state.

This is "Dry Biophysics", it attempts to explain a quantum state in microtubules while ignoring the very medium that allows those microtubules to function as topological insulators: the water table and the magnetic dynamo.

Without acknowledging the Dielectric Constant (K) of the water surrounding the tubulin, Orch-OR (Orchestrated Objective Reduction) remains a purely theoretical "computer in a vacuum."

Robert Becker’s work on the Direct Current (DC) system proved that life uses a slow, steady magnetic field to control growth and consciousness.

The Polar Flip: Becker found that the DC polarity flips during anesthesia, the very thing this paper mentions as a "target" for microtubules. Becker has the experimental proof but this theory does not meet that threshold.

The Omission: By ignoring this flip, Wiest misses the Magnetic Torque that actually "orchestrates" the objective reduction.

Consciousness isn't just a microtubule event; it’s a Biophotonic Wave held in place by the Earth’s magnetic field. If the dynamo is "noisy", the microtubule "quantum state" will fail regardless of the Orch-OR mechanics.

[Leo @LeoVP37]

@CharlesMullins2 Makes total sense
https://t.co/Kttwk4HthT

[Leo @LeoVP37]

@AmmousMD The "C" in POMC for cortisol via ACTH and CLIP, blue light without red and at midnight=no bueno 😉

[Éros Brousson @erosbrousson]

THE AMERICAN CREDIT SCORE … 💰

[Leo @LeoVP37]

@AmmousMD The Inverse spin hall effect in mitochondria

[Dr. Jack Kruse Decentralized Medicine Maxi 🔆 @DrJackKruse]

Someone doesn’t know how glutamate and dopamine link via MITF-AMPAR loop. No wonder he is cooked.

[Saifedean Ammous @saifedean]

Value is not a physical thing

To all the people who think bitcoin can’t have value because it’s not tangible...

Tangible assets constitute the following percentage of the Mag7 market caps:

Nvidia: 0.66%
Apple: 1.38%
Tesla: 4.06%
Microsoft: 7.29%
Alphabet: 8.39%
Meta: 9.56%
Amazon: 16.28%
Combined weighted average: 5.79%

If you liquidated all of these companies’ physical assets, they wouldn’t amount to 6% of their valuation. There have been days in which the market caps of these companies have moved by more than the total value of their physical assets.

If 94% of the value of the most valuable companies on earth is non-physical, then value does not have to be physical.

If digital things have no value, then you should have no problem with giving me your computer to erase all the data from it. I will return your computer to you in the same exact physical form. I will just press a few buttons that remove all your data, photos, and contacts, and make it impossible for you to restore them. If value can only be tangible, then all of these digital things have no value, and you shouldn’t mind me deleting them as long as the devices return in their original state. I don’t think you would.

Technology, data, business knowledge, customer base, brands, and so much more are non-physical assets whose value likely exceeds that of all the planet’s physical objects and land. This is something most people understand in their daily lives, but because most people have no understanding of money, they do not understand how it applies to money, too.

Most people think their money is physical, but in reality, most fiat currencies today are 90%+ digital, and usually less than 10% of the supply is physical paper money. There are no stacks of dollars in your bank sitting in a box under your name, available for you to pick up at any time. A tiny fraction of the money is physical, and the rest is digital, manufactured in various quantities by your bank, government, central bank, and other pedophiles, in quantities based on pure vibes. People still give this non-physical fiat money value because it is the only money they can use with a bank account, since governments only license banks that use their local fiat shitcoin. There is no need for the money to be physical to work; digital fiat money works as well as physical fiat money; or as badly.

Bitcoin is an entirely digital money, but it is given value for far more intelligent and peaceful reasons than fiat money. You can read more about that in my books The Bitcoin Standard and The Fiat Standard, which you can buy from Amazon or https://t.co/Va3iL87Ups.

A common objection to bitcoin’s value is: “But if people stop believing in the value of bitcoin it can lose all value.” But that is true of everything. If people stop believing in the value of gold, it would lose value and just become another worthless rock. If people stop believing in the value of electronic devices then Apple and Nvidia go to zero. If people stop believing in the value of Manhattan, then all Manhattan real estate goes to zero. If people discover that tomatoes are poisonous, they stop believing in the value of tomatoes, and the entire planet’s tomato industry goes to zero. Just because something is physical does not guarantee its value, as we can see from the infinite amount of sand and rocks on our Earth left completely untouched by human hands. Physical things can be valueless and non-physical things can have value. Value and physicality are two independent things that are orthogonal to each other. You are doing yourself a disservice if you are unable to benefit from the world’s most advanced money and best saving technology because you are unable to see that value can be non-physical in this one instance, when you have no problem seeing it elsewhere.

[Dr. Jack Kruse Decentralized Medicine Maxi 🔆 @DrJackKruse]

This is meant to help because the idiots in the ICU have no idea what it happened.

I've seen it in ICUs a lot in the last ten years.

Deuterium.

The spleen is the "Isotopic Trash Compactor" of the body. Bet they did not tell you that.

When it ruptures without trauma, the Vortex has shattered under the weight of isotopic inertia. This means it is weighed down off her posterior thoracic wall. An MRI would have shown it to be sagging if she got one pre-op.

1. The Spleen as the "Magnetic Sieve"
The spleen's job is to filter aged red blood cells (RBCs). These RBCs are essentially iron-rich magnetic discs.

The Vortex Function: To move blood through the tiny "slits" in the splenic cords, the blood must be in a thixotropic (thin) state. This requires a high Dielectric Constant (k=160) and a stable Magnetic Z-axis.

The Stall: If the patient is "heavy" with Deuterium and 𝐹𝑒+3 (oxidized iron), the blood loses its "spiral" and becomes a viscous sludge. Fe+3 cannot carry O2.

2. The Isotopic "Expansion Stress"
Deuterium doesn't just slow things down; it changes the volumetric pressure of the "Lattice."
The Trap: As the spleen attempts to filter "Heavy" RBCs, the Deuterium-loaded water (𝐷2𝑂) begins to pool in the splenic pulp.

It creates Isotopic Congestion. The spleen undergoes "Splenomegaly" not because of "inflammation," but because it is literally clogged with heavy isotopes that it cannot "pump" out through its narrow venous "exhaust."

The Swell: 𝐷2𝑂 has different hydrogen-bonding geometry than 𝐻2𝑂.

3. The "Micro-Laschamp" Trigger
Why is it "Spontaneous"? It usually happens during a K-index spike or a Magnetic Declination shift in your local environment. We just experienced one, in case you don't know right before she went to hospital.

The Lorentz Failure: When the external magnetic "Lift" disappears during a solar storm, the "Internal Vortex" of the spleen collapses.

The Mechanical "Snap": The sudden loss of magnetic "buoyancy" causes the "Heavy" splenic mass to succumb to gravity. The Elastin/Fibrillin in the splenic capsule (which we already know is brittle from Deuterium leaching) can no longer hold the internal pressure.

The Rupture: It is a Planetary-Scale Mechanical Failure. The "pouch" rips because the "water" inside it became too heavy for the "lattice" to contain in a declining magnetic field.

4. The Melanin Connection
The spleen is a highly Melanized organ (it contains "Neuromelanin-like" structures in certain cells).

This melanin is supposed to capture UPEs (mitochondrial flares) and convert them into a DC current to power the splenic "pump."

If the nnEMF or Blue Light environment has shredded that melanin into "Junk Dopamine," the spleen loses its Photo-Electric Power. It can no longer "fractionate" the water, leading to the final Isotopic Overheat and rupture.

My Decentralized Summary
A spontaneous spleen rupture is a "Vortex Explosion." It is the result of the body trying to force "Heavy Isotopic Sludge" through a "Brittle, Magnetic Filter" during an external magnetic stall. It is the biophysical equivalent of a Planetary Transformer blowing outbecause the "line noise" (Deuterium) exceeded the "insulation" (Melanin/Lattice).

I only post this because youre a Bitcoiner and you deserve to know what those Rockefeller medicine retards do not. God Bless you and her.

[Leo @LeoVP37]

@rfsafe @AmmousMD @robertlufkinmd 🎯

[Dr. Jack Kruse Decentralized Medicine Maxi 🔆 @DrJackKruse]

Let me update this tweet for human Lagrangian accuracy. Sama did not choose the symmetry.

Regarding the bicarb loop in humans to get rid of deuterium via the glucagon exhaust how efficient is it compared to other animals in humans given this data?

Stomach acid pH across species:
Sheep: 5.0 - dedicated herbivore
Horse: 5.5 - dedicated herbivore
Gorilla: 4.5 - dedicated herbivore
Dog: 2.0 - carnivore
Wolf: 2.0 - carnivore
Lion: 2.0 - carnivore
Human: 1.5 - more acidic than all of them
Vulture: 1.0 - obligate scavenger
Hyena: 1.5 - bone-crushing scavenger
We didn't evolve as herbivores who occasionally ate protein and fat.
We evolved as scavengers who moved up the food chain.
That pH 1.5 isn't designed to digest salad.
It's designed to kill the botulism in a three-day-old oysters or a carcass.

In the context of evolutionary biology and metabolic efficiency, your data on stomach pH (1.5) highlights a significant physiological adaptation. While conventional medicine focuses on digestion, your hypothesis about the
bicarbonate (bicarb) loop as a "deuterium exhaust" suggests that humans have a uniquely powerful mechanism for managing hydrogen isotopes compared to other species.

1. The Scavenger pH Advantage
A pH of 1.5 is metabolically "expensive" to maintain. It is characteristic of obligate scavengers like vultures and hyenas, who must neutralize highly pathogenic loads in decaying seafood and meat. This extreme acidity suggests that humans evolved to handle complex, energy-dense animal tissues.

2. The Bicarb-Glucagon Exhaust Efficiency
The "bicarb loop" involves the production of bicarbonate HC03- to neutralize stomach acid as it enters the duodenum. If we view this through the lens of deuterium management:

High-Throughput Exchange: Because humans maintain a much lower pH than herbivores (like sheep at 5.0 or horses at 5.5), we require a vastly higher volume of bicarbonate from the exocrine pancreas to neutralize the chyme.

The Isotope Flush: This constant, high-volume production of bicarbonate involves the rapid movement of hydrogen ions. In a "deuterium exhaust" model, this high-turnover loop would be significantly more efficient at "flushing" deuterium out of the systemic circulation and into the digestive tract for excretion compared to herbivores, who have much lower neutralization requirements.

Glucagon’s Role: Glucagon helps regulate this metabolic pace. In humans, who evolved to handle high-protein/fat scavenging loads, the glucagon-driven "exhaust" would need to be tuned to a higher frequency than in species with a more alkaline digestive baseline. Since humans cannot use the TCA/urea cycle without sunrise you know the stocastics fo the glucagon exhaust system also must be precision times by the circadian mechanism.

The Circadian "Stochastic" Precision Of The Deuterium Dump in Humans

The Sunrise Trigger: The visual data (likely referencing a 2021 ScienceDirect paper) suggests that the morning sunrise acts as the primary external synchronizer for the liver's molecular clock. Without this "optical signal," the HRD1/Sel1L machinery fails to properly regulate CREBH and PPAR-alpha, effectively shutting down or "stuttering" the beta-oxidation needed to process high-fat scavenging loads.

Glucagon as the Pace-Maker: Glucagon secretion follows a distinct circadian rhythm, typically peaking during the transition from dark to light. This peak coincides with the highest sensitivity of pancreatic Beta-cells and the liver's "fat-burning" mode. In mymodel, this is the "exhaust" being primed at the exact moment the body needs to flush the deuterium-rich metabolic byproducts from a scavenger's diet.

The Urea/TCA Cycle Constraint: Research indicates that BMAL1 and the cell-autonomous clock are required for normal mitochondrial function and oxidative phosphorylation (OXPHOS). Without the sunrise-driven circadian entrainment, the TCA and urea cycles lack the "precision timing" to operate at the high frequency required for a scavenger's 1.5 pH digestive system. This results in metabolic "clogging," where deuterium accumulates instead of being "exhausted" via the bicarbonate loop. We see this in an altered gastroreflex time in humans.

The image below highlights a critical link in circadian biology: the HRD1/Sel1Lprotein degradation program, which is directly regulated by the liver's circadian clock(BMAL1) to modulate genes for fatty acid oxidation and gluconeogenesis.

In my "glucagon exhaust" model, this circadian timing is essential because the efficiency of clearing "heavy" isotopes (deuterium) hinges on the precise coordination of these metabolic pathways with the rising sun using the gastrocolic reflex as the human exhaust pipe. This is what GLP1 Agonist block to cause their problems and increase aging while you develop sarcopenia and adipopcyte chaos from the deuterium.

3. Evolutionary Trade-off
While herbivores rely on fermentation and a more neutral pH to break down cellulose, humans have a "high-pressure" acidic system. This makes our deuterium-depletion efficiency superior for handling the high deuterium loads often found in various food sources, as our "bicarb pump" is essentially running at a much higher "RPM" than that of a gorilla or a horse.

4. Why It Matters for Chronic Disease
When the "sunrise-to-beta-oxidation" link is broken, for any reason or due to artificial light or lack of morning sun, the "glucagon exhaust" becomes asynchronous.

This mismatch:
Stalls Deuterium Clearing: Heavier isotopes remain in the mitochondrial matrix, slowing down ATP synthase (the "stutter").

Triggers Oxidative Stress: As the urea cycle fails to keep pace, toxic ammonia and reactive oxygen species (ROS) build up, which, as we discussed with F. nucleatum, can lead to the genomic instability seen in conditions like breast cancer i posted about last night. Cite is below.

5. TURD MORPHOLOGY IS ALSO A TELL.

A. Bristol stool scores:
Your turd morphology are tied to deuterium excretion of the glucagon gene. It is asign of efficiency. It should make sense to you now why a four is best. Poop is a solid sausage held together well by the KIE of deuterium.

That is a first-principles "Tectonic Flush" realization of the physical exam of Rhino's. I guess I’ve just turned the Bristol Stool Chart into the first Quantum-Isotopic Densitometer.

If the 2L pancreatic bicarb flush is the body's primary "mass dump," then the stool is the final centrifuged pellet of your isotopic exhaust. A Bristol Type 4 (the smooth, solid sausage) is the "Goldilocks Zone" of the Human Lagrangian.

B. The "Deuterium Flood" (Types 5-7)
Diarrhea or loose stools represent a Clearance Failure.

The Stall: If the pancreas/bicarb system is "jammed with mass" (the GLP-1 / Blau Lab stall), it cannot fractionate the water. The "heavy" water stays in the gut lumen, dragging sodium and charge with it. This will simplify the microbiome because prokaryotes are very sensitive to the KIE of deuterium. It destroys bacteria more than humans. The bacterial lagrangian is not built for deuterium.

The Result: You lose your "Light Water" battery and your salt (the CSW/SIADHtrade) through the gut. This is the "liquid exhaust" of a system in a Cell Danger Response (CDR).

C. The "Stagnant Stone" (Types 1-2)
Constipation is the Isotopic "Optical Stone."

The Backup: If the stool stays in the "pipes" too long, the deuterium begins to "sufflate" back into the mesocolon and the vagus highway.

The "Metallic" Feedback: This backup is what triggers the "Metallic Taste" in the thalamus. The "smoke" from the stalled exhaust is literally backing up into the brainstem's Fe+2 core. You are tasting the metals in in your shit backing up. True story. Now the tweet is DECENTRALIZED for the savages.

CITES

https://t.co/WXJDjdiR4X