Dr. Morse has zero clue what ultrasound does to water in a tendon over time. If he did he would not help you facilitate your future torn Achilles tendon. If you want prevention do not screen. Walk on a beach with your feet in the water every AM, begin using grounding shoes, and use the abscopal effect of sunlight on your skin to increse the piezo electric and flexoelectric strength of solar photons to strengthen your tendons and joints.
You do not have to come to El Salvador to see me. I offer you this Rx here on X for free. You can asked Adrian Peterson, Drew Brees, or Cam Akers. We use biophyscis and quantum biology to help our trainers and athletes.
In centrlaized medicine where ultrasound screenings are used this is what they do not tell you: Using conventional orthopedic management most of these injuries requiring 9–12 months on average. See Dan Marino. Achilles tendon ruptures are severe injuries in the NFL, with historical return-to-play (RTP) rates around 60–70% and typical timelines of about 11 months for those who do return.
The first person who used decentrlaized ideas was Jerry Rice for his ACL. See how that went. He came back in same season. See TO. Broke his leg in season and played in SB that same season.
See AP.
Tore his ACL and embraced the suck of decentralized ideas and ran for 2000 yds the next yr. See 2012 T Suggs. Tore his Achilles and came back in 6 months to play in the last SB the Ravens won with Harbaugh.
Tom Brady began to use naked sunbathing to fuel his play to 47 yrs old after a KC Safety took his ACL out. These are the things centralized medicine has made fun of at your expense. Aaron Rogers uses decentrlaized medicine to come back from his ACL and is playing tonight. The media and retards made fun of his use of cold and darkness with him walking the beach in malibu as he came back at over 40 yrs old. That was a very un- Marino think Aaron did a few years ago.
Do you want to be like everyone else and do ultrasounds on you achilles or do you want to put the extra in ordinary to do what the few in the NFL have? Embrace the suck of Nature to come back fast.
2. Let us ask the question Dr. Morse is too ignorant to raise, namely, what are the effects of using ultrasound on coherent domains in water? It is well established in the literature that for collagen to keep its piezo and flexoelectric abilities to performs it must be well hydrated by CCO from heme proteins. So what does screening ultrasound do to the collagen matrix in the Achilles based on what is known?
3. Ultrasound used in medical offices is considered by water researchers to be high intensity. Did you know this? I know the good doctor Morse doesn't because he has never read a water journal in physics in his life. If he had, he'd never have invited anyone to Miami to use a high intensity ultrasound machine to screen them. WHY?
4. High-intensity ultrasound used in centralized medicine screening tends to disrupt coherence (via cavitation or shear), while low-intensity or targeted applications may enhance or manipulate it through phonon-mediated interactions. These papers are all published in physics journals and water journals for you to read. I hand them out to my professional athlete clients and tell them to never let their TRAINERS near them with a ten foot pool if they are carrying an ultrasound machine.
These findings are backed by experiments in fields like quantum biology and water research. They remain controversial ONLY mainstream science who uses ultrasound to make money.
What does medical ultrasound cause?
5. Ultrasound, as high-frequency acoustic waves in screening devices, can interact with these coherent domains through mechanical pressure, cavitation, or phonon coupling, leading to various deleterious effects The effects depend upon level of heteroplasmy in the ligament, how much damage is done to CCO by a lack of proper grounding and solar exposure, the of use intensity, frequency, are all contextual.
What is the other problem.
It destroys the photomolecualr effect found in water because of heat generation.
I bet most centralized MDs have never heard of this effect because they are too busy reading up on the food pyramid.
Loss of this effect is like putting sunglasses in front of CCO in your achilles tendon because it disrupts ELF-UV signaling in mitochondria.
I tell all my atheletes if I ever see you wearing sunglasses or using ultrasound I will fire you. Below is why.
6. Use of ultrasound also eliminate the pyroelectric effect in water. What is that one?
Not only do sunglasses do this, but this is why I won't let my guys get their nails on hands or feet be covered with any toxic substance to prevent future injury.
Caleb Williams carries this risk.
7. The last quantum biological process US destroys is flexoelectricity. This is the ability of tendons, ligaments, discs, ....etc to retain their memories of what optimal triple helical function is under any stressor. Once flexoelectric currents are lost in collagen an injury is for sure coming.
How?
This disruptive effect is relevant in superirradiance biology in biological water networks. This was what Montagnier was realy studying in his 2009 paper on water that I mentioned to Huberman in the Tetra podcast. Ultrasound can be used to improve or negate its ability to remember electromagnetic signaling from UPEs. Pseudoscientific people call this "a control mechanism to negate "memory" effects."
Decentralized science understands that solitons are used at night during sleep to restore tissue when skeletal muslce are parlyzed in sleep cycle to erase poor redox patterns you acquired during activity.
Ultrasound exposure has been shown experiementally to break down coherent domains, particularly in scenarios involving "water memory". The creation of DDW from CCO is how water increases its ability to be imprinted by light photons.
This flexoelectric ability is how water retains information from dissolved solutes from tissue damage. most collagen is surrounded by different water than CCO makes. So when DDW is created it dilutes high deuterium extracellular water derived from the blood (slide below) with DDW to allow tisues to erase redox damage to repair itself photo bio-electrically.
This disruption eliminates the biological or physical effects associated with these structures, similar to thermal denaturation. This effect mirrors heating water to 70°C for one hour, suggesting ultrasound induces mechanical shear or vibrational energy that destabilizes the quantum-coherent oscillations. Flexoelectric effects RESTORE this healing ability in collagen.
For instance, in studies on water memory mechanisms, ultrasound has been shown to completely abolish the biological efficiency of substances like histamine, implying it dismantles underlying nanostructures such as chains of nano-pearls or ferroelectric crystallites that support coherence.
These are the foundational reason my clients avoid high intensity medical screening ultrasound. You do not have to pay me for this info. Decentralized medicine wants all to use it.
I write about all this for clients and they become first principle thinkers and become problems for the centralized MDs trainers, and food guru influencers.
That is how I roll. I show them Nature's plan in using flexoelectricity to their benefit when a bolt fo lightening hits a tree and the tree remains undamaged. I want to turn my athlete clients into that tree and not the one who explodes because the tree in your neighbor's yard is loaded with big Ag chemicals and fertilizers that ruin this effect in your trees.
8.
9. I copy this blog and hand it to all my athletes with collagen and soft tissue injuries. patreon.com/posts/cpc-30-g…
10. People struggle to understand how scales changes how things can act in Nature.
For example, so if atoms are 99.999999999% empty space… what happens if we magically squish out all that emptiness and only keep the actual "stuff" (the nuclei and electrons)?
All 8 billion+ people on Earth, every bit of their real physical matter, would fit inside something about the size of one ordinary sugar cube!
11. You are mostly empty space, but the forces and patterns in that space make you perfectly real, solid-feeling, and amazing. It makes your collagen appear strong.
Matter isn't about being "stuffed full" , it's about clever organization, energy, and invisible rules holding everything together in collagen. With respect to it, water chemistry is one of the key EM forces involved. Few realize it.
Light at small scale is by far most important.
12. Light give collagen is uber strength. This is why centralized clinicians and trainers think small amount of UPE photons from mitochondria and blood cannot do amazing things, yet the inverse square law teaches us that as scale shronks the EMF on Earth get uber strong.
13. What Are UPEs, Really? (The "Tiny Candle" Analogy) UPEs are spontaneous, ultra-low-level light emitted by all living cells as a byproduct of normal metabolism which arise mainly from mitochondria during oxidative reactions (ROS like singlet oxygen or excited carbonyls relaxing and releasing photons).
Typical detected intensities outside cells are very weak:~10–1000 photons per second per cm² (often tens to hundreds under normal conditions, higher with stress). This translates to roughly 10⁻¹⁶ to 10⁻¹⁸ W/cm² (or even lower in some estimates).
Analogy: Think of a single UPE source in a cell as a tiny, flickering birthday candle in a pitch-black football stadium at night.
From far away (outside the cell), you barely notice it, it's almost invisible. But if you're right next to it (nanometers away inside the cell), that little flame feels blindingly bright because the light hasn't spread out yet.
Mainstream science sees UPE as a byproduct of metabolism (especially mitochondrial ROS), useful for monitoring oxidative stress, but not necessarily a purposeful "signal."
Some researchers (like in microtubule or coherence models) propose it could play roles in intracellular signaling, repair, or circadian sync with my decentralized thesis of "mitocepcion" because this idea aligns with those emerging hypotheses.
14. What if I told you the little UPEs in you are more powerful than the sun and this is why your ligaments derive their stregth.......would you believe me?
Well it is true.
The Inverse Square Law Magic: Why Nanoscale Makes "Tiny" Huge
The inverse square law says intensity (I) drops with the square of distance (r) from a point source:I = P / (4πr²) (where P is the power emitted by the source)
My calculation in the pic above can be fact checked but you'll find they are spot-on for a hypothetical single source emitting 10⁻¹⁹ W (a very low value, but illustrative for one reaction/event): At r = 1 nm (10⁻⁹ m), I ≈ 8 × 10⁻³ W/m² = 8 × 10⁻⁷ W/cm².
That's orders of magnitude higher than typical external detections! At cellular scales (nanometers between molecules like mtDNA, proteins, or neuromelanin), local intensity skyrockets because the photons haven't spread out over a large area yet.
Analogy: Imagine whispering in a quiet room from across the room, it's inaudible. But whisper directly into someone's ear (1 nm scale), and it's loud and clear. As scale shrinks distance, so the "signal" (intensity) explodes even a whisper becomes a shout.
This is why skeptics who say "UPE is too weak to matter" miss the point: they're measuring it from afar (macro scale). Inside the crowded nanoscale world of a cell, the local flux can be biologically relevant, especially if absorbed by nearby light-sensitive molecules (aromatic amino acids in proteins, flavins, or melanin complexes).
This is why I tell you to stop caring about the opinion of idiots who opinion never mattered because they do not know the basics of how life really works.
15. Centralized science often struggles with scale. Macro measurements make UPE seem insignificant, but the inverse square law shows how potent these photons become at the nanoscale where biology actually happens.
My decentralized thesis beautifully highlights light's primacy, because cells aren't just chemical machines; they're electromagnetic orchestras tuned to subtle photon patterns. Class 4 lasers are a better choice than an ultrasound machine and they might/could be a tool to "turn up the volume" on those natural signals for healing, as long as we respect the dose (excess = stress mirror).
My perspective should be profound to the injured athlete because they all aligns with emerging ideas in quantum biology (coherence in microtubules, mitochondrial waveguides).
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@MaxGulhaneMD I do have to say after the first 20 minutes I like the discussion but I was frustrated in spots where he was physics facile as he could have been but it is clear Nunn believes as I do that biology is not fundamental it is biophysical.
He is too much in love with Levin. Levin has do nothing to advance Becker.
But I want to tell you at the 1:10 mark you bring up CCO and DDW. Nunn seems uncomfortable.
He goes on to talk KIE boilerplate but he is a biochemist and is dabbling in biphysics so you need to push and extend him further on the D/H+ isotope selection process tied to photosynethesis creation of deuterium on the carbon backbone. there has to be a way to sort the isoptopes and there is biophysically but I do not think he knows what it is.
DDW, heat, and UPEs are exhaust products from matrix operation. He seems to know this. But so is CO2. He does not seem to know the biophysics of CO2 and its real purpose.
The Failure of Centralized "Exhaust" Logic is always on display with Nunn here.
Centralized medicine tries to "fix" CO₂ levels or pH chemically, failing to realize they are tweaking the isotopic selection process that uses magnetic tuning of a quantum circuit.
High CO₂ isn't just "acidosis"; it is the cell trying to increase its "Hash Power" and protect its internal water from the "Double-Spend" attack of entropy I describe in my thesis. CO2 is dimagnetic. this means it shields CCO from the magentic fields of the matrix. Ask yourself why? The answer is simple biophysics. It guarantees that H+ is pushed into the intermembrane space so the ATPase has it to use to spin the Fo head. Deuterium has a different magnetic moment so CO2 acts to sort it and keep it away from the Intermembrane space so that the nanotorque engine is not slowed or destroyed. Neither, Nunn, Boros or Somylai know this because they are blinded by biochemical BS.
So because you asked the question he could not answer he is the answer:
The Physics: CO₂ is highly diamagnetic. By concentrating it at the site of water creation (CCO), the cell creates a FOCAL magnetic "quiet zone."
The DC Current: This allows the protons (H+ not D) to flow in a coherent DC current of repair without being scattered by the "vibrational noise" of the environment.
The VDR Link to the shied: The VDR sitting on the IMM acts as the sensor that ensures the CO₂/O₂/Light ratio is tuned to keep this magnetic "shield" active.
VDR: The Photonic Antenna that directs electron flow, speed, and tunneling efficiency before cytochrome C
Fe-S/CCO: The Quantum Engine is the engine that allows electron and proton tunneling
Carbonic Anhydrase in the matrix/CO₂: The Magnetic Shield/Tuner selects the stochiomtery H+ inside the intermembrane space to deliver to the ATPase.
This mechanism is sorting engines into "good/health/CCO and bad/Disease/Cardiolipin/heteroplasmy to get rid of the bad via Cardiolipin, or to extend life with DDW from CCO to hydrate all our semiconductive proteins. Timing from the OUTSIDE environment photonic signals controls this process max. Recall how Vitamin D, Melanin, DDW, NO, and CO2 are all made. Outside in, not inside out. Biochemists always have the inside out framework because this is where biochemistry occurs. Outside in is where biophysics of life begins.
The Calcium-Melanin Nexus: Macro vs. Micro Control
My thesis identification of melanin's macroscopic chelation vs. Vitamin D’s stochastic sorting provides a complete picture of cellular calcium management:
Melanin (The Macro-Buffer): Melanin acts as a high-capacity reservoir that absorbs and stores calcium. Certain light frequencies allow its release. Vitamin D made from 312-320 nm exogenous light on cholesterol esters is sent inside to the kidney and liver for final processing. This binds the VDR on the IMM and it is the VDR that can get into the nucleus to alter it way after the photonics of this axis acts first with clock genes.
This "macroscopic chelation" of melanin provides a stabilizing background, preventing the "vibrational noise" of the environment from immediately overwhelming the cell's delicate electric circuits.
Vitamin D/VDR (The Stochastic Sorter): Sitting on the Inner Mitochondrial Membrane (IMM), the VDR acts as the "fine-tooth comb." It performs stochastic sorting, precisely directing individual Ca²⁺ ions to the TCA cycle dehydrogenases to tune the "Hash Power" (metabolic flux) based on the UVB/IR signals received from the exterior. VDR binding isolates CCO with CL.
The 30 Million Volt Charge: This charge on the IMM is the physical manifestation of the DC current of repair. It encodes photonic information as a voltage gradient, allowing the matrix to "read" the external environment through the language of electron and proton tunneling.
2. Other point @MaxGulhaneMD more for you than him. He does not seem to understand an additional neutron = more mass and as mass goes up what does Ilya theory from his Nobel in 1977 say? Timing slows.
So any additional mass irrespecitve of a KIE means that heteroplasmy expands because in CCO you have the story of life and death. A lot of H+ = CCO makes water and CO2.
Too much D+ and it stimulates Cardiolipin. Boros keeps confusing you with broken engines. They do not break. D+ cannot fit in the channel. The ATPase starves and the matrix swells and this stimulates forced apoptosis.
Decentralized Internal light Medicine done by the non visual photoreceptors is "Tuning the Shield"
The VDR, the Fe-S clusters, and the Carbonic Anhydrase system form a Triad of Temporal Control distally to the RPE-SCN.
The CO₂ Diamagnetic Shield
In my model, CO₂ provides the low-entropy environment required for the Protonic Spin-Ice (EZ water) to form. If you look at proton tunneling it is best modelled in ice. What these biochemistry guy don't yet relaize is when melanin is hydrated by DDW you create massive proton tunneling and you open more of the biophysics Pandora box like Grotthaus etcs........
3. The Solar vs. nnEMF Split: "Quantized" ROS
My slide below highlights the critical difference in how the cell processes Solar EMF vs. nnEMF (5G/Malware):
Solar EMF (Quantized Information): Sunlight creates a highly specific and sensitive amount of Reactive Oxygen Species (ROS). This is not "damage"; it is quantized information delivered via UVA/Blue light-stimulated Nitric Oxide (NO).
The NO Filter: UVA light controls NO production, which reversibly inhibits Cytochrome c Oxidase (CCO). This acts as a frequency filter for the DC current, preventing the "Double-Spend" entropy attack.
nnEMF Malware (Non-Quantized Noise): Unlike the sun, 5G/nnEMF acts as a Voltage-Gated Calcium Channel (VGCC) disruptor. This causes a massive, non-quantized "leak" of Ca²⁺, leading to:Hydroxyl Radical Flood: The resulting Fenton chemistry creates Hydroxyl Radicals (the most destructive ROS).
Photoreceptor Destruction: This noise "blinds" the internal lighting system of the non visual photoreceptors, leading to mitophagy failure and broken apoptosis, leaving behind a "static colony of defective mitochondria" (the hallmark of chronic disease/cancer).
Sorry @MaxGulhaneMD but I chuckled so hard listening to th first 20 minutes of this. When is this guy going to realize that Dr. Pirogine theory on dissipative structures has at its core a TIME SYMMETRY aspect. He still does not get it. Even at the Guy foundation they fly blind.
At life's genesis because of dissipative theory energy was always a commodity, but Time is the real value. He has no idea about the implications of this.
Evolution of life happens because life costly in time, not in energy because of the equations link to entropy.
this idea scales from stars to cells. A supernova has massive energy flux, but it is a state of total chaos (High Entropy). A human brain has much lower energy flux but evolved to have massive Temporal Coherence.
Each "event" in a cell, like a proton tunneling through a molybdenum transistor enzyme in mitochondria or a biophoton hitting a melanin sheet, is a "Block" in the ledger. It’s not "good" or "bad"; it’s a physical State Transition. Wisdom is the ability of the organism to maintain that ledger’s integrity against the "Double-Spend" attack of entropy. Sorry your expert fell short because he is ignorant about the 1977 Nobel Prize implication for mammals. youtube.com/watch?v=y5DEQ1…
2. Life is costly in time not energy goes right back to the 1977 Noble Prize. At life's genesis chaos has to gain order. Dissipative structure theory really aims to solve this problem for biology by using physics.
Dissipative structure theory led to pioneering research in self-organizing systems, as well as philosophical inquiries into the formation of complexity on biological entities and the quest for a creative and irreversible role of time in the natural sciences.
There is a well-known theorem of minimum entropy production derived by Prigogine, which states that entropy exported from a system reaches a minimum, or becomes zero, at thermodynamic equilibrium and at steady states close to thermodynamic equilibrium. Prigogine's theorem is a direct consequence of Onsager's reciprocity relationship which holds at steady states close to thermodynamic equilibrium. The principle of internal entropy compensation, is in addition to, and implies the principle of minimum entropy production, and may even be valid in regimes far from thermodynamic equilibrium.
He had some very interesting things to say about TIME in his work and Nobel Prize speech. I think they are key to understanding circadian biology and timing. All of our time reversible equations in physics created by Newton, Einstein, and Schrödinger describe a simplification of what actually occurs in nature. We live our lives with eyes blinkered, dismissing reality as the exception to our neatly formed approximations of what time really is.
3. Prigogine’s work on Minimum Entropy Production explains why mammals must be "Costly in Time & not in Energy".
By proving that Time is Irreversible, he effectively "Hard Forked" biology away from the time-reversible approximations of Newton and Einstein. Time reversibility is built into the matrix. That is heteroplasmy. As it changes so does time you experience.
Near equilibrium, entropy production is minimized. But life exists far from equilibrium, much to the dismay of all your food guru friends. To maintain complexity, the organism must "export" entropy. This is why life innovated clock genes quick. They are flow meters for entropy.
My historical and political analyses have compared
the QAnon phenomena before DJT presidency (45th) and the 1920s Soviet counterintelligence operation "Operation Trust" (Operatsiya Trest) due to their shared use of psychological manipulation to pacify political opposition. If you review my twitter feed you'll see no QAnon posts because I believed they were counter ops of the Zionist controling Israel at this time. Bibi was that leader. He was reaching back into the Zionist bag to the take over of Russia in 1917.
The parallels between these two movements typically center on the following tactics:
"Trust the Plan" Narrative of 4D chess: Both movements relied on the central premise that a secret group of high-ranking insiders, patriots within the government or military, was working covertly to dismantle the regime from within.
Neutralization of Dissent: Operation Trust was designed by the Soviet secret police (Cheka/GPU) to create a fake anti-Bolshevik resistance (the Monarchist Union of Central Russia). Its primary goal was to convince opponents to wait for this "internal coup" rather than taking active measures, effectively stalling real resistance.
Discrediting Opposition: When Operation Trust was exposed in 1927, it humiliated those who had believed in it, making them appear foolish and reducing their willingness to support future anti-Bolshevik efforts.
Luring and Identifying Targets: Just as QAnon encouraged followers to identify themselves online, Operation Trust lured high-profile dissidents like Sidney Reilly and Boris Savinkov back to Russia, where they were captured or executed.
QAnon was part of the plan to turn MAGA to MIGA, in my opinion. The same thing that went on in Russia in 1917 is ongoing in Washington DC.
2. Palantir surveillance will be used to target those who went against this coup and they will be taken care of by the zionist faction that wins this coup between the bankers and transhumanist tech bros.
3. Point three as proof of the current coup of America by MIGA:
You missed a big lesson. The "Green Revolution" Pipeline of the 1940-2025 = Melanin Erasure Program
The Rockefeller/Monsanto/Sperry Rand trinity wasn't just about "feeding the world"; it was about standardizing the human bio-frequency.
The Inputs: Rockefeller provided the "seeds," Monsanto provided the "chemical metal-shredder" (Roundup), and Sperry Rand provided the "computational logistics" to scale this melanin-destroying diet globally.
The DARPA Connection: By canceling Robert O. Becker’s lab, DARPA protected this industrial model. They couldn't allow the world to know that we are DC bio-electric organisms whose health depends on the semiconductive fidelity of the melanin that the Green Revolution was designed to erase.
2. Room 5600: The Professionalization of Biotech Warfare
J. Richardson Dilworth was the architect of the financial "Pivot." He shifted the Rockefeller "Room 5600" from 19th-century industrialism to 21st-century Biotech Control.
The Venrock Ecosystem: By seeding Amgen and its peers, the family office created a "Multi-Client" trap. They funded the discovery of Leptin (1994) specifically because they already knew from the DARPA MKULTRA program that melanin was the key target to hit in farming. Glyphosate is a competive inhibitor of melanin. Few know it.
The Shelved the Leptin Trials: When the leptin trials showed that Light and Cold were the actual regulators of the pathway, they couldn't commercialize that, because there’s no profit in the Sun. So, they shelved the "Photonic" truth and pivoted to the Distal pathway below photonics and elevated the GLP-1 Agonists to treat the symptoms of the light-starved world they built in the 1960's BigTech revolution in Silicon Valley. Steve Jobs links to Rockefeller and Rothschild is deep.
The connection between Steve Jobs and the Rockefeller and Rothschild families is primarily rooted inearly-stage venture capital, shared high-level board memberships, and modern institutional investment. While Jobs was an adopted child of a working-class couple, his career in Silicon Valley was deeply intertwined with the financial infrastructure established by these dynasties.
The Rockefeller family’s venture capital arm, Venrock Associates, was one of the early investors in Apple Computer during its start-up phase in Silicon Valley. This initial capital was crucial for transitioning Apple from a hobbyist project into a scalable corporation. Venrock's involvement established a direct link between the Rockefeller family office (established in 1882) and the nascent personal computing industry.
The Rothschild family has maintained a significant financial interest in Apple through various investment vehicles:Rothschild Investment Corp: This firm identifies Apple Inc. (AAPL) as one of its top holdings in recent SEC filings.
RIT Capital Partners: Chaired by Lord Jacob Rothschild, this London-listed trust acquired a 37% stake in Rockefeller Financial Services in 2012, formally uniting the two dynasties' wealth management interests.
Laurene Powell Jobs, Steve Jobs’ widow, serves as a bridge to the elite policy circles traditionally associated with the Rockefellers:Council on Foreign Relations (CFR): Laurene Powell Jobs serves on the board of the CFR, an organization famously chaired by David Rockefeller from 1970 to 1985.
Ford Foundation: She also sits on the board of the Ford Foundation, another pillar of the philanthropic network where the Rockefeller influence is historically substantial
Jobs is often compared to John D. Rockefeller in terms of his business impact. While Rockefeller revolutionized industry through vertical integration, Jobs transformed technology through a closed ecosystem that redefined global consumer behavior = Why the Epstein emails call Jobs brilliant. Jobs and John D. Rockefeller integrated their business just like Groves did in the Manhattan Project. Go re listen to my Podcast with Breedlove on Groves.
Few can rival my research. I am all over these fuckers.
3. The Savage's Survival Guide
The "Centralized PhDs" are merely the maintenance crew for the Rockefeller/Amgen/Monsanto grid. They are trained to ignore the RPE-SCN-POMC circuitry because acknowledging it would dismantle the entire $100 million "Leptin Bounty" and the trillion-dollar pharmaceutical "Distal Patch" industry.
Uncle Jack, the warning to the Savages is clear:
Glyphosate is a "Metal Leaking" agent.
Blue Light is a "Timing Shredding agent."
Leptin Resistance is a "Power Outage" signal.
The Monk must not only sell his Ferrari; he must burn the Rockefeller "Roadmap" and reconnect to the DC Bio-Electric Current of the Sun.
How do we begin the "Melanin Reclamation" for the Savages who are currently trapped in the Green Revolution/Agenda 2030 isotopic sink?
Why doesn't Rockefeller centralized medicine work for 99.9% of people?
It is designed to make the family customers not deliver cures for the people.
This is why in Norway right now, below your ability to know it, because zionist media is quiet on it while they feed you Bondi nonsense (circus maximus), they are ransacking the house of the Nobel Committee leader. Jagland. LOL... bastards... Norway the perfect country for corruption.
This is why Epstein was at Harvard and MIT and why Maxwell family controlled PEER review in centralized science. It is why Robert O. Becker was cancelled by the front people (Dr. Phillip Hnadler) for Rockefeller Medicine. The entire scheme was designed to keep Rockefeller medicine in power. Few. Eric Weinstein wants to know why Epstein was in his math dept at MIT. This is why. Control the scientific narratives, control what gets funded and published, control what gets studied and what get buried to Pubsmear (Elisabeth Bik) and then you auction off Nobel Prizes and give them to researchers whose science leads to no cures.
@Kevin_McKernan @JesslovesMJK
2. Why doesn't Rockefeller centralized medicine work for 99.9% of people?
It is designed to make the family customers not deliver cures for the people.
This is why in Norway right now, below your ability to know it, because zionist media is quiet on it while they feed you Bondi nonsense (circus maximus), they are ransacking the house of the Nobel Committee leader. Jagland. LOL... bastards... Norway the perfect country for corruption.
This is why Epstein was at Harvard and MIT and why Maxwell family controlled PEER review in centralized science. It is why Robert O. Becker was cancelled by the front people (Dr. Phillip Handler) for Rockefeller Medicine. The entire scheme was designed to keep Rockefeller medicine in power. Few. Eric Weinstein wants to know why Epstein was in his math dept at MIT. This is why. Control the scientific narratives, control what gets funded and published, control what gets studied and what get buried to Pubsmear (Elisabeth Bik) and then you auction off Nobel Prizes and give them to researchers whose science leads to no cures.
1.x.com/DrJackKruse/st…
2.x.com/DissidentMedia…
3.x.com/DissidentMedia…
4.x.com/DissidentMedia…
DID YOU READ THE NEW MKULTRA BLOG YET? patreon.com/posts/cpc-78-n…
3. Are you paying attention Savages? I doubt it.
A new, compact, high-power microwave weapon, the TPG1000Cs, has been developed at a Shanghai Nuclear Technology Institute, which could become one of the most serious threats to the Starlink satellite network.
The device can deliver 20 gigawatts of energy for up to a full minute, the South China Morning Post reported, cited by Portfolio.
The TPG1000Cs, the world’s first compact driver for high-power microwave weapons, has been created at the Northwest Institute of Nuclear Technology in Shanghai. The device can deliver 20 gigawatts of power for up to one minute.
At just four meters long and weighing just five tons, the device is small enough to be mounted on trucks, warships, airplanes, or even satellites. Some Chinese experts estimate that a ground-based microwave weapon with a power of over 1 gigawatt could be capable of seriously disrupting or even damaging satellites in low Earth orbit, such as Starlink, being used in the Russian-Ukrainian war.
Previously known similar systems could operate continuously for no more than three seconds and were much larger. The Russian Sinus-7 drive, for example, was operational for about a second, delivered about 100 pulses per shot, and weighed up to 10 tons.
China has repeatedly signaled that Starlink poses a serious threat to its national security. Chinese military researchers are currently developing new “Starlink killer” weapons, including high-powered microwave systems and lasers, that could be used to relatively cheaply combat large constellations of low-orbit satellites if necessary.
SpaceX has lowered the orbital altitude of its Starlink satellites to reduce the risk of collisions. But that makes them much more vulnerable to attacks from ground-based directed energy weapons. If China eventually deploys the TPG1000Cs in space, the invisible strikes could be even more devastating.
Erika Kirk family DEW Microwave weapon was used to harvest Maduro from Venezuela so the Zionist could cpature the oil and refine it in Citgo refinies in the USA that one of Miriam fiends just bought on the courthouse steps for 7 billion. YOU'RE SLEEPING.
This new blog is more explosive than the Epstein files, that I promise.
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Richard Helms, the Director of Central Intelligence, ordered the destruction of the vast majority of CIA MKULTRA documents in January 1973. He believed these were all the records. The original MKULTRA work was done at Tulane University in the Dept of Neurology and Neurosurgery in the 1950s and 1960s and he was unaware of this. Much of that work was linked to the Tulane Primate lab. Delgado's work in bulls was copied by the Tulane researchers.
The program, first began with drugs moved to wired technologies and then ended in wireless technology using polarized light from screens. Final patents for screen use to control the nervous system of humans were filed in 2003 by people known to be linked to US government contracting and DARPA. The drugs were given to primates and humans. The program involved administering Mexican Peyote and LSD and other drugs to unwitting human subjects, was highly controversial, illegal, and immoral. Helms ordered the destruction of the files during a period of intense scrutiny following the Watergate scandal and as he was leaving office.
Helms sought to erase the evidence of the planning and approval of these test programs to prevent public outrage and ensure no one would be prosecuted. He also knew about the rumors of forming the Church Comission which was being done to examine and audit the illegal activities in the CIA at this time. Frank Church was a Senator from Kentucky. As Helms was forced to resign by President Nixon in 1973, he ordered the purge as one of his final acts to protect the agency and his subordinates.
He left an executor behind to finish the job of document destruction. The Executor was Sidney Gottlieb. I spoke about him briefly with RFK Jr in the Rick Rubin Tetra podcast. The destruction of MKULTRA was authorized by Dr. Sidney Gottlieb. He was the head of MKULTRA, who ordered the files shredded. The chief of the CIA Records Center protested the destruction of these files on February 2, 1973, but the order was carried out anyway. Despite the 1973 order, a cache of approximately 20,000 documents survived because they were misfiled in financial records rather than subject files, which were discovered in 1977.
In 1989-1991, I found a cache of 16 boxes of MKULTRA data from the Tulane University Dept of Neurology and Neurosurgery. All the science in this blog was discovered in those boxes in the basement of Charity Hospital. Charity Hospital was flooded by by Hurricane Katrina in 2005. The NOPD and NO Fire Dept said that the basement areas were flooded all assets of the hospital were destroyed and cleared as salvage. I've referenced what I found in many podcasts but this blog contains the hardcore science data I found and I put together as a resident at LSU neurosurgery. The CIA sought to prevent congressional investigators from discovering the extent of the experiments, which involved over 80 institutions including universities and hospitals.
2. The collateral effects of the blog above for kids stuck in the Rockefeller paradigm of medicine?
Jaundice, Heteroplasmy, and Transgenerational Epigenetics: The Warning Flare that shows up in the NICU.
The baby's matirx becomes loaded with atoms it cannot use to clear the toxin. Bilirubin build up in the skin and brain alter the fluorescence of both organs and this changes how both organs work. Normally UV fluorescence is a function of cholesterol and melanin in the skin and brain.
Bilirubin can significantly interfere with the UV fluorescence and light absorption properties of the skin, though it doesn't do so by changing the melanin itself. Instead, bilirubin acts as a "competitive absorber" and a fluorophore in its own right. Here is how that interaction works:
1. Absorption Overlap
Melanin is a broad-spectrum absorber, meaning it soaks up light across almost the entire UV and visible spectrum. Bilirubin, however, has a very specific "peak" absorption around 450–460 nm (blue light).
When you shine UV or near-UV light on the skin:
Melanin absorbs the light to protect the lower layers.
Bilirubin absorbs the light in that specific blue-green range.
The Result: If you are looking for the specific "glow" (fluorescence) of melanin or other skin components, the presence of bilirubin acts like a yellow filter, "stealing" the light before it can reach the melanin or blocking the resulting fluorescence from reaching your eyes/sensors.
2. Bilirubin’s Own Fluorescence
Bilirubin is actually fluorescent under certain conditions. When exposed to specific wavelengths of light, it can emit its own glow.
In medical diagnostics, researchers use skin fluorescence spectroscopy to measure bilirubin.
If you were to look at the skin under a Wood's Lamp (UV blacklight), high levels of bilirubin can alter the expected reflection. While melanin usually looks dark/void under UV, bilirubin can introduce a "muddy" or sickly hue that masks the crispness of the melanin's appearance.
3. The Phototherapy Connection
This relationship is actually the basis for treating jaundice in infants. We use Phototherapy (blue light) because:
Bilirubin absorbs the light energy.
That energy triggers a chemical reaction (photoisomerization).
The bilirubin changes into a water-soluble form that the body can excrete.
The Melanin Factor: This is exactly why phototherapy is LESS efficient in babies with high melanin levels. The melanin "competes" for the light, absorbing it before it can reach the bilirubin in the blood vessels, often requiring a higher intensity of light for treatment. NICU's stopped using UV light in my training!!!!
^^^^This is why when I was in medical school I always asked why we went away from UV light to treat jaundiced kids and the answer I always got back was retinal hyperplasia damage. I pointed out that studies all had medotholgy problems, never considered skin pigment levels and were sponsered by Rockefeller medicine foundation. They advocated for blue even thought blue light would add more mass to the childs matrix and age it right in the hospital. It was infuriating.
Jaundice in a baby which is yellow skin from bilirubin buildup (5-20 mg/dL vs. normal <1) screams trouble, and it’s tied to my decentalized dance. It’s a neon sign of heteroplasmy that mtDNA mutations piling up in utero, skewing the Fe²⁺/Fe³⁺ atomic fulcrum. The baby is adding mass to its body for no reason at all. Then you add in all the metals from the jabs they get. No wonder they are not all cretins.
Pregnancy gone wrong (hypoxia, ROS spikes, maternal stress) loads fetal tissues with defective mtDNA (10⁻⁵/bp/division, 10x normal). Bilirubin, from heme breakdown (Fe²⁺ oxidized to Fe³⁺), floods when liver mitochondria falter and this affects cytochrome c oxidase (Cu, Fe) and Q-cycle stall (NADH/NAD+ ratio +50%, per neonatal studies). You should have seen the faces of the OB's when a neurosurgery resident call them idiots when I showed them how the Q cycle worked. They are dumb asses.
NO binds Fe²⁺ too long (g = 2.03 persists), O₂ starves (pO₂ < 20 mmHg), and biophotons dim (10⁴ photons/cm²/s, sluggish growth and horrible repair is inborn in the kid in the ICU and the centralized fucks do not know it. Parent have no idea what their light addiction just caused.
Transgenerational epigenetics seals it; maternal mtDNA lesions (8-oxo-dG up 3x, per oocyte sequencing) pass down, amplified by ROS (0.5 mM in utero). Paramagnetic sync with Earth’s field frays that Fe²⁺/NO can’t toggle, Co/Mn falter, VEGF lags (angiogenesis -30%). your babies germ line has a 30% higher heteroplasmy rate.
Jaundice flags this: a baby’s tissues, choked with heteroplasmy, can’t regenerate like Becker’s kids did with torn off finger tips because voltage drops (+2 mV early), biophotons fade (10³ photons/cm²/s), and Fe³⁺ dominates (g = 4.3). It’s epigenetics 101 and the pregnancy’s chaos scars the next generation’s electromagnetic web. Not bueno at all. Rockefeller medicine is like going to the Zorro Ranch with no cell phone.
3. Dynasties must fulfill their destinies. Paradigms are like dynasties. Paradigms, like Rockefeller medicine must enforce their dynasties. Nature is different because life is nature’s dynasty.
My decentralized thesis strikes the final chord of the Quantum Biological Manifesto. I
’ve identified that the "Manufactured Dynasty" of modern medicine is essentially a Thermodynamic Lie; a sprawling edifice of "obfuscations and equations" designed to ignore the singular, simple truth that Life is a Light-Mediated Time Crystal.
When the environment (the conditions of existence) is decoupled from the internal "Nockchain," the dynasty of Nature is overthrown by the chaos of entropy.
The "Truth" is simpler than any equation: We are beings of Light, governed by Time.
The "Dynasty of Nature" can only be restored when we stop trying to "push and pull" our biochemistry with mechanical interventions.
We must return to the Conditions of Existence that created us: The Morning Sun, the Cold, the Ground, and the Sunset "Fountain of Youth."
Decentrlaized medicine shifts the MDs perspective by moving medical practice from Rockefeller "Pharmacological Management" to "Environmental Engineering." It acknowledges that the clinician’s role is not to "fix" the patient with material inputs, but to restore the Quantum Coherence of the patient's internal matrix so the body can heal itself according to the laws of physics.
My curiosity has revealed the "Nockchain" of reality. The only question remains: Are we brave enough to delete the manufactured dynasty and live by the laws of the Sun?