Morris Barney Dalitz = Mr. Las Vegas is how the link between the Mossad, CIA, and mob occured when Vegas was being built. He also was who the CIA interviewed about the one armed bandits and blocking our sunlight in the casinos to increase revenue from more gambling.

He worked in his family's laundry business early in his life during WW1, but began a career in bootlegging when the Prohibition era began by Constitutional decree in 1919. Here is where he learned about the link between behavior, alcohol abuse, during night time with ALAN. He capitalized on his access to the laundry trucks in the family business to bootleg. As a consequence, he developed a partnership with the Maceocrime syndicate which ran Galveston, Tx during the roaring 20's and supplied liquor from Canada and Mexico. This business was massive and he was so profitable that this is how the mafia came to give him the oasis in the desert to develop using behavior modification, alcohol, solar blockade, and use of electrical lighting in gambling/drink houses to addict people to spend their money.

In 1982 it was clear he was Mossad when, Dalitz received the "Torch of Liberty" award from the Anti-Defamation League of B'nai B'rith. This chapter is a Mossad front. Dalitz and a group of Cleveland investors purchased the Desert Inn, which opened in 1950, after founder Wilbur Clark ran out of money for the project.
Dalitz tapped an investment group who included Donald Stralheim, who changed his name to Stralem due to anti semitism in NYC during WW 1. Stralem married Jean Lehman Ickelheimer, a member of the Lehman family that ran the Lehman Brothers investment bank, on April 11, 1928. He was very connected with the banker families linked to the new Federal Resrve Bank created in 1911-13 by JP Morgan and friends.

In his bootlegging days Dalitz learned the gambling alcohol business from Meyer Lansky. In 1949 American Municipal Association, representing more than 10,000 cities nationwide, petitioned the federal government to combat the growing influence of organized crime. First-term senator Estes Kefauver of Tennessee drafted a resolution to create a special committee to investigate the issue. The Commerce and Judiciary Committees ran the investigation, and Vice President Alben Barkley cast the tie-breaking vote to establish a special committee. It was here we learned how Dalitz linked to the Jewish mob and Mossad. Lansky was always in the cross hairs of the FBI/CIA but Dalitz was keep uber clean by his handlers. If police detectives, CIA/FBI suspected Dalitz of wrongdoing, they dared not whisper such criticism without ample evidence because of his link with Israeli defense. By the time Dalitz reached his prime later in his life, his financial empire and formidable string of businesses were legitimate. He was the perfect front man for Israeli Intelligence.

Post WW2 in America the heat was on as law enforcement and high-ranking politicians vilified illegal gamblers and their ilk as a societal scourge.
Moe Dalitz did what any businessman with acumen might have done. He migrated to Las Vegas, Nevada where casino games were legal and gamblers were respected. At the time, Las Vegas and Havana, Cuba vied for dominance as legal gambling centers. The Italian mob of Carlos Marcelo ruled the Cuban casino scene. Dalitz spent time in Cuban casinos learning modern gaming, where his friend and bootlegging ally Meyer Lansky had invested many millions. Because of JFK and RFK Sr, Meyer Lansky and the Israeli syndicates lost millions of dollars due to the Bay of Pigs fiasco. This is why the US gov't and mob became joined in their hatred for the Keneedy brothers.

In Vegas, Moe Dalitz became good friends with Teamsters union president Jimmy Hoffa, and consequently had access to millions of dollars in loans from the Teamsters Central States Pension Fund. Bobby Kennedy Sr hated Hoffa and went after him mercilessly as AG under JFK.

Moe became linked to David Rockefeller and several Mossad agents assigned to Rockefeller congressional staffers (pre AIPAC organization) by Israel's lobby by way of B'nai B'rith in the late 1940s. This continued into the 1950s. Dalitz got private financing from the friends of the Rockefeller's for the Desert Inn purchase which got him into the Vegas casino scene when Wilbert Clark went bankrupt. Nelson Rockefeller was tapped to provide private financing for Dalitz via his connections.

Nelson brother, David Rockefeller had a financier partner whose name was Donald Stralem. This guy was the son of the co-founder in 1850 of Rothschild affiliate Hallgarten & Co., German-Jewish investment bankers that financed both sides in the Civil War. This is how the bankers and Israel got into Vegas early even before the Italian mob did. Moe Dalitz was the guy. Once Cuba went boom in 1959, then Lansky's krewe became interested in Vegas because of his links to Dalitz.

The link of Nelson to JFK's murder is via Warren Commission member Gerald Ford. Nelson served as the 41st vice president of the United States from 1974 to 1977 under President Gerald Ford who was appointed President after Nixon resigned. Nelson, like Nixon was member of the Republican Party who had deep links to the oil businessmen in Texas who were in on the assassination I mentioned to Abel James in his podcast. Nelson Rockefeller served as the 49th governor of New York from 1959 to 1973. Rockefeller also served as assistant secretary of State for American Republic Affairs for Presidents Franklin D. Roosevelt (Note the link here to Gen Groves and Henry Wallace debacle) and Harry S. Truman (1944–1945 CIA link) as well as under secretary of Health, Education and Welfare (HEW) under Dwight D. Eisenhower from 1953 to 1954. Nelson was the son of John D. Rockefeller Jr. and Abby Aldrich Rockefeller and was the grandson of Standard Oil co-founder John D. Rockefeller whose Oil company was broken up by Teddy Roosevelt after McKinley was assassinated in 1900. Now you can see more of the links tied to the @AbelJames pod I did.
2. Meyer Lansky was born in Grodno, Russia (now Hrodna, Belarus). In 1911 the family emigrated to the United States and settled on the Lower East Side of Manhattan, New York. While Lansky was in school, he allegedly met young Charles "Lucky" Luciano, who tried to shake him down (extort money). When Lansky refused to pay, Luciano was impressed with the younger boy's bravery and the two became friends for life. Lansky met Bugsy Siegel when he was a teenager. They also became lifelong friends, and together with Luciano, formed a lasting partnership. Lansky was instrumental in Luciano's rise to power by organizing the 1931 murder of Mafia powerhouse Salvatore Maranzano. As a youngster, Siegel saved Lansky's life several times, a fact which Lansky always appreciated. The two adroitly managed the Bug and Meyer Mob despite its reputation as one of the most violent Prohibition gangs. Lansky was the brother of Jacob "Jake" Lansky, who in 1959 was the manager of the Nacional Hotel in Havana, Cuba.

By 1936, Lansky had established gambling operations in Florida, New Orleans, and Cuba. This was the same year that his partner Luciano was sent to prison. As Alfred McCoy records: "During the 1930s, Meyer Lansky 'discovered' the Caribbean for northeastern syndicate bosses and invested their illegal profits in an assortment of lucrative gambling ventures... He was also reportedly responsible for organized crime's decision to declare Miami a 'free city' (i.e., not subject to the usual rules of territorial monopoly)." Later, Lansky convinced the Mafia to place Siegel in charge of Las Vegas, and became a big investor in Siegel's Flamingo Hotel project. After Al Capone's 1931 conviction for tax evasion & prostitution, Lansky realized his own vulnerability to this type of prosecution. In response, he transferred illegal funds from his growing casino empire to Europe, where he opened a numbered bank account with the Rothschild banks following the 1934 Swiss Banking Act. Later, according to Lucy Komisar, Lansky would buy an offshore bank in Switzerland (Rockefeller's had one as well), which he used for money laundering through a network of shell and holding companies. Politicians and bankers have used banks to do this for hundreds of years.
3. In the 1930s, Meyer Lansky and his gang stepped outside their usual criminal activities to break up rallies held by Nazi sympathizers. Lansky recalled a particular rally in Yorkville, a German neighborhood in Manhattan, that he and 14 other hoods disrupted: The stage was decorated with a swastika and a picture of Hitler. The speakers started ranting. There were only fifteen of us, but we went into action. We threw some of them out the windows. Most of the Nazis panicked and ran out. We chased them and beat them up. We wanted to show them that Jews would not always sit back and accept insults. This is where B'Nai B'rith formed alliances with Lansky.

For many years, the ADL anw now AIPAC has been linked to Jewish organized crime because of Lansky and Dalitz. In fact, the ADL gave, Moe Dalitz, their "Torch of Freedom" award in 1980s for his donating millions of dollars to the state of Israel. Donations from Dalitz, who headed the Cleveland mob known as the Mayfield Road Gang, allegedly came from his ownership of Las Vegas casinos such as the Desert Inn. I became aware of how money was laundered when I was a teenager working as a runner for banks in NYC.

Take a look at the Las Vegas Review-Journal article "The Double Life of Moe Dalitz" by John L. Smith, explains Dalitz' background in their series "The First 100 Persons Who Shaped Southern Nevada" (at ).

"Early in his life, Dalitz was a bootlegger and racketeer mentioned in the same breath as (Jewish) Meyer Lansky and (Jewish) Benjamin "Bugsy" Siegel. In Cleveland, one longtime member of law enforcement would tell the Kefauver Commission, 'Ruthless beatings, unsolved murders and shakedowns, threats and bribery came to this community as a result of gangsters' rise to power.' Dalitz was considered part of that rise."

Theodore Silbert worked simultaneously for the ADL and the Sterling National Bank (a mafia operation controlled by the Lansky syndicate). He lived in the Pentahouse apartment of 936 5th Ave for years. His apartment overlooked what would become Waldenberg Park that DJT repaired on behalf of ADL/AIPAC lobbyists.

Mira Lansky Boland, the granddaughter of notorious Jewish mafia boss, Meyer Lansky, was described in a Village Voice article by Robert Friedman of May 11th, 1993, as the ADL's top 'fact-finder' in Washington, DC. The links are there if you want to examine them. The truth is that the ADL of B'nai B'rith is anti-Gentile and anti American. They are not about anti-defamation, but their whole modus operandi is concerned with defaming anyone of any nationality who wants for their own people what the Jewish ADL leaders what for theirs. They work in unison with AIPAC in Washington DC now. How did AIPAC begin? Lansky gave the ADL the idea of AIPAC.

During World War II, Lansky was also instrumental in helping the Office of Naval Intelligence's Operation Underworld, in which the US government recruited criminals to watch out for German infiltrators and submarine-borne saboteurs.
According to Lucky Luciano's authorized biography, during this time, Lansky helped arrange a deal with the US Government via a high-ranking Navy official. This deal would secure the transfer of Lucky Luciano to a minimal security prison; in exchange the Mafia would provide security for the docks in New York Harbor. German submarines were beleieved to be entering the harbor at this time undetected, and there was great fear of attack or sabotage by Nazi sympathizers. (See "The Merger", by Paddy Kelly for detailed account).1st100.com/part2/dalitz.h…
4. Once Lansky and Dalitz were done who did the Mossad turn too to run their Las Vegas laundering schemes? nytimes.com/2021/01/12/bus…
5. Did you know that J.P Morgan and 50 of his banking friends, some of whom were in favor of the creation of the Federal Reserve, decided not to board at the last minute? Those who were not in favor it, stayed on the boat. For those of you who think 9/11 was the first run of a government psy-ops by the bankers, you need to know more about history. Stop watching Netflix and listen to food influencers.Image
6. With the help of a friendly mainsteam media, paid off congresspeople in the legislative branch who have their own AIPAC handle, the ADL's b'mai b'rite has become the premier lobby for Israeli interests in America, and the source of hate crime legislation by Congress and curtailment of First Amendment freedom of speech through their attempted censorship of the Internet. You need to understand history to understand modern current events. Millenials and Gen Xers, Gen Z's have no idea what they do not know.

Hopefully some of you will wake up. Listen to Tucker Carlson Podcast with Massie and tell me it does not make sense now.Image
7. The Mob prefers a bank patronized by the CIA, since both are involved in illegal activities, only the CIA calls its work covert action. When Lansky died Adeilson got schooled by Alvin Malnick on how to launder dirty cash through certain banks into art and real estate and emerge as men who seem clean and not connected to organized crime. Malnick was the sole heir to Lansky's fortune when he died. Malnick drove the developement in San Diego and Miami using Lansky's money in the 1970's- 2000's after he learned the game from Lansky in the 1960s. In the 1960s, Miami lawyer Alvin Malnik set up the Bank of Commerce in the Bahamas. Mob money flowed into its secret numbered accounts by the hundreds of millions--from mob financier Meyer Lansky's money, most of it--and then out again into Tibor Rosenbaum’s International Credit Bank of Switzerland before returning to the United States for investment in the real estate and art world. Why do you think Adelson and Steve Wynn hotels were filled with art worth millions of dollars? That is the legacy of Dalitz and Lanskey. Fiat bankers are their bitches laundering money. Malnick is why we have AML/KYC laws and I bet not more than 5 Bitcoiners know who Malnick is.

Any bank that serves the CIA by funneling agency money into covert work must hide the trail through paper fronts, and such fronts are precisely what organized crime needs to wash its dirty money. It also became apparent that some bank- ers deliberately blurred their relations with government agents and mobsters, using a CIA cover to protect their criminal con-nections. But in a number of cases it was not only the banker who clouded the lines but also the CIA, which was working with gangsters, supposedly for political motives but occasionally for the personal enrichment of its agents, as appears to have been the case in the Nugan Hand Bank scandal in Australia.Image
The answer to the second question lies in the changed nature of banking and the size of criminal profits. In the past mobsters infiltrated many industries but rarely bothered with banks because they were not spectacularly profitable and were too conservatively run. Moreover, the underground economy was still limited in size and had no overwhelming need of banks. All that has changed since the 1970s, with the exponential growth of money markets and a parallel explosion in profits from crime, particularly the drug trade which was ideal for CIA laundering for covert operations for the industrial military complex. This is the real reason Ross Ulbricht got the sentence he did. He was cutting into the profits of the CIA/FBI machine. This system of exchange now earns more than a trillion a year in untaxed profits and ranks as the United States' second biggest industry after oil. This is why your government allows an open border and invites Fentanyl into the US. Your family is being used as a vampire victim of the government need for cash to run forever wars.

The answer to the second question lies in the changed nature of banking and the size of criminal profits. In the past mobsters infiltrated many industries but rarely bothered with banks because they were not spectacularly profitable and were too conservatively run. Moreover, the underground economy was still limited in size and had no overwhelming need of banks. All that has changed since the 1970s, with the exponential growth of money markets and a parallel explosion in profits from crime, particularly the drug trade which was ideal for CIA laundering for covert operations for the industrial military complex. This is the real reason Ross Ulbricht got the sentence he did. He was cutting into the profits of the CIA/FBI machine. This system of exchange now earns more than a trillion a year in untaxed profits and ranks as the United States' second biggest industry after oil. This is why your government allows an open border and invites Fentanyl into the US. Your family is being used as a vampire victim of the government need for cash to run forever wars. Now they have a new patsy in Ukraine and Zelensky. This is why the Uniparty votes as they do.Image
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9. AIPAC and B’nai B’rith have many elves in history acting as fly paper. Image
10. Now for the biggie connections: FDR to the Royal family, the bankers, Lansky by way of the polio vaccine and Salk. All tied to the pre civil war migration of a group of men who knew Queen Victoria's new husband and they became spies for the Crown in NYC. How did it all go down?Image
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11. Franklin D Roosevelt was criticized by conservatives and libertarians for his economic interventionism that did nothing to end the Depression.
Despite all the President's efforts and the courage of the American people, the Depression hung on until 1941, when America's involvement in the Second World War resulted in the drafting of young men into military service, and the creation of millions of jobs in defense and war industries.  This is how General Groves got the idea that military spending on defense contractors was a prudent move for the country.  The bankers and Industrialist realized it was another new opportunity for them to launder money from federal contracts.  This is how the industrial military complex was born in 1939-1941.  Charles Lindberg was a huge opponent of FDR and the military for this reason.

Lindberg most famous quote captured his beliefs around FDR and the military.  He said, "If I had to choose between nature or man, I would rather have birds than airplanes. Real freedom lies in wildness, not in civilization. In time of war, truth is always replaced by propaganda. It is the greatest shot of adrenaline to be doing what you have wanted to do so badly."  People forget he quit the military in 1941 and resigned his position.  The FDR administration waged a smear campaign (with the help of the ADL chapter of B'nai B'rith) against Lindbergh that blighted his reputation forever.  FDR wanted to enter WW2 contrary to what your history books say today.  Lindberg saw the military provocation done at see from his plane that clearly told him FDR was much more of a war mongering President than history says he was.  Because of this Lindberg political views became opposite FDR.  He was a strict isolationist.   Today Lindberg is forgotten.  But when I was a young boy my grandparents told me he was remembered as a great aviator who later endured personal tragedy, and during World War II, was a German sympathizer with antisemitic beliefs.  That last part came from FDR's liaisons with the ADL.

Lindberg became FDR's opponent when he publically challenged Roosevelt's decision to cancel the commercial air mail contracts and later as a proponent and spokesman for the America First Committee (ADL group), a group which supported America's nonintervention in the European war. That Roosevelt was successful in his campaign against Lindberg is demonstrated by the memories and perceptions of those contemporaries I had polled.

In 1940, a group of Yale University students founded the America First Committee to oppose US intervention in the European war. They quickly mobilized hundreds of other antiwar students to join the organization, and persuaded one of the nation’s most outspoken isolationists, Charles Lindbergh, to support its cause. Lindbergh’s enormous celebrity—dating to his 1927 solo, nonstop flight across the Atlantic Ocean—helped the America First Committee become a national organization with as many as 800,000 members.  After Lindbergh accused Jews of being “war agitators” in a speech at Des Moines, Iowa, on September 11, 1941, the America First Committee’s reputation changed significantly. Newspapers and magazines across the country denounced Lindbergh and the committee for promoting antisemitism and intolerance. Political cartoonists, including PM newspaper artist Theodor Geisel (Dr. Seuss), accused Lindbergh of spreading Nazi propaganda. America First Committee leaders denied the accusation, but the criticism continued.   Geisel was an ADL member.  The ADL fueled this propaganda against Lindberg to assist FDR efforts.  The ADL, UK Prime Minister, and House of Windsor were all on the same team behind the scenes and Lindberg never knew it.  Neither did We The People.  B' nai B’rith ( also called Sons of the Covenant) is the oldest Jewish fraternal organization in the world. It was founded in 1843 in America by a small group of German immigrants who came from the UK.  Most of them had links to the Saxe-Coburg-Gotha a capital of the duchyin Germany.  In the nineteenth century, prior to 1848, no Jews were permitted to live in the duchy of Gotha, although they could trade there under restrictions; after 1848 they were free to enter. This is why many of the B'nai B'rith Jews left in 1840-43 to go to America to start anew in a land where they could start fresh.  You should know this community had a literary society and a B'nai B'rith lodge present at this time.  They were British loyalists.  They opposed the American Revolution and they instigated many problems during the Civil War because of their ties to the British Monarchy.  They became very helpful to the Monarchy.

How did the link get strengthened in 1840 pre civil war?    The name Saxe-Coburg-Gotha came into the British Royal Family in 1840 with the marriage of Queen Victoria to Prince Albert, son of Ernst, Duke of Saxe-Coburg & Gotha. Queen Victoria herself was the last monarch of the House of Hanover. The House of Saxe-Coburg-Gotha as a British dynasty was short-lived because the family name had to changed as a result of anti-German feeling during the First World War, and the name Windsor was adopted after the Castle of the same name.  the King Of Germany was cousins with the King of England and they caused the first WW1.  This is when the British Empire began its collapse and loss of power.  Today's events via the WHO/WEF/and ADL are attempts to regain that power by weakening America's Constitutional Republic by corrupting its branches of government.  The blueprint was seen at the beginning of WW2 when Churchill promised the King he would do all he could to draw America into the war to fight its battles with Germany again.

FDR was easily manipulated by Winston Churchill as the former maneuvered or was maneuvered into bringing the United States into World War II. Another revelatory fact was how Churchill "...was determined from the beginning to turn the United States into a combatant in WW2 with the help of the ADL.

In January of 1941, one poll found that 88% of Americans opposed the idea of declaring war against the Axis powers in Europe. As late as June of 1941, only 35% of Americans believed their government should risk war to help the British.  On December 6th 1941, Japan gave FDR his chance and the Pearl Harbor attack completely changed public opinion overnight.  Did you know that ADL chapter of  B'nai B'rith was part of British Intelligence at this time?  So few Americans know their own history well enough and this explains why many of things are going on today. Few will recall that John McCloy was our Secretary of the War at this time in the USA.  did you know he wound up on the Warren Commission after the JFK assassination?

Your government is controlled by a shadow government that would stun you if you knew the scope of the corruption.   Ukraine and Afghanostan are just the latest opportunities for the shadow government to launder money to clandestine military operations that the industrial military complex mandates from the Executive and Legislative branches. Both parts are captured parts of government.  Much of that laudering goes through the UK airports today into the Middle East and flows back to Tel Aviv and the government there.

The DNC and the executive branch has a robust history of in this sort of corruption.  FDR is remembered as a hero not a traitor.  Some of us who know better think he and Biden have a lot in common.

CITES













exhibitions.ushmm.org/americans-and-…
reaganlibrary.gov/archives/speec…
tovima.com/wsj/billions-i…
americanussr.com/american-ussr-…
latimes.com/archives/la-xp…
nytimes.com/2021/01/12/bus…
jrbooksonline.com/adl/adl/behind…

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More from @DrJackKruse

Mar 16
Why does what she is saying in this video make decentralized sense biophysically?

Here is a breakdown of how the biophysics perspective connects to biochemistry to quantum signaling in the microbiome: @SabinehazanMD

1. The Pancreas as a Deuterium Sink
From the biophysics perspective, it’s about mass export.The secretion of ~2L of bicarbonate (𝐻𝐶𝑂−3) daily isn't just about neutralizing 𝑝𝐻.

Carbonic Anhydrase II (CAII): This enzyme serves as the kinetic gatekeeper. By rapidly hydrating
𝐶𝑂2
with water, it effectively captures the hydrogen (or deuterium) from the intracellular matrix and shunts it into the intestinal lumen.

Deuterium Clearance: If the body preferentially uses "light" water (𝐻2𝑂) for ATP production in the mitochondria to prevent "stuttering" in the ATP-synthase motor, the exocrine system must have a massive exit strategy for the 𝐷2𝑂 it accumulates. What happens to prokaryotes in a high deuterium back up system? The prokaryotes die off and simplify.
The bicarbonate system is that high-volume exit that keep deuterium moving to your shit so it does not stunt the growth of your microbiome.

2. Melanin and Isotopic Fractionation
The presence of a massive amount of melanin in enterochromaffin cells suggests a role beyond simple pigmentation or "tanning." That role is using the radically different magnetic moment of deuterium compared to H+ to chealte deuterium to get it out of the gut via the gastrocolic reflex.

Symmetry Breaking (SU2): Melanin acts as a semiconductor and a "magnetic trap." Because deuterium has a different magnetic moment and mass than protium, melanin can utilize its paramagnetic properties to fractionate these isotopes.

The Gut-Brain Optical Link: If melanin is managing the flow of isotopes, it is also managing the optical density of the tissue. Deuterium-laden water alters the vibrational frequencies of the hydrogen-bond network. A "backup" in this system, would cause a less diverse microbiome and/or melanin dysfunction—acts like "smoke" in the exhaust, clogging the biophotonic signaling that the brainstem monitors via the vagus nerve and the transverse mesocolon pathways.

3. Improving ΔΨ = improving the 30 million volt charge of the IMM in the brain.
Your conclusion about the microbiome is critical here. Prokaryotes are most aafected by the KIE of deuterium because of how they make energy. When the proton gradient is contaminated with heavy deuterium, the efficiency of the matrix drops, the "voltage" of the cell falls, and signaling to the brainstem reflects a state of metabolic "stress" or low energy. This unleashes the mitochondrial retrograde response where GDF-15 skyrockets, AMPAR goes nuts, brainstem glutaminergic signaling is off and this stimulate the CDR. This is a state of emergency event for the brain. This leads to altered brain function. The vagus nerve is the conduit where that transmits this infomation from the gut to the brain. The CDR signal sets off the Transdermal MITF-AMPAR signal and this begins to destroy melanin creation in all neuroectodermal derivatives.

Microbiome as the Evolutionary Cleaner: A healthy pancreas processes the "exhaust" (the bicarbonate and isotopic waste).

When this system backs up for any reason, kids brains have to work on the old atavistic Pax software package and they cannot think well (AMPAR) and their thalamus becomes defective because in children who's brain is still developing post natally the thalmus serves as the cite where neurogenesis occurs to build out the CNS post natally. Vagus is the highway connecting the two organs. This back up of deuterium will also stunt muscle growth in the small bowel and lead to slowed gastric and duodenal emptying times. The children will have many GI symptoms along with psychological changes.

In my model, healing the gut isn't about "digestion" in the traditional sense; it’s about restoring the quantum transparency of the body's exhaust system so the mitochondrial motors in the brain can run on high-voltage protium and not have their IMJ's filled with deuterium.

My biophysics explanation of Dr. Hazan clinical findings is profound expansion of the "exhaust" model of what a defective glucagon gene exhaust problem is. I'm describing a thermodynamic bottleneck where a failure in isotopic clearance triggers a systemic "state of emergency." This is happening in people using GLP 1 drugs too. The difference is, their brains are already built out by 25 years old so the same effect is not seen. They are cognitively impaired and the AMPAR part of this equation is now well laid out why. A recent paper from Yokahama University explains why cognition is impaired in long COVID when the AMPAR system is blocked.

By integrating the Cell Danger Response (CDR) and the Kie (Kinetic Isotope Effect), you’ve pinpointed why GI distress and neurodevelopmental delays (like those seen in autism or Pans/Pandas) are often two sides of the same coin. MDs and parents are stumped by these conditions but my tribe is not. I told @NicoleShanahn exactly how this operates when I wrote a blog for her daughter called QE #45 on Patreon.

My Keys Refinements to Dr. Hazan's Microbiome Model:

The Prokaryotic Filter: If the pancreas fails as a deuterium sink, the duodenal deuterium load rises. Because bacteria lack the complex isotopic shielding of eukaryotes, "heavy" water acts as a metabolic toxin. This forces the microbiome to simplify and revert to atavistic strains that can survive the "stuttering" motors, essentially killing off the diverse "evolutionary cleaners" needed for high-level signaling.

The GDF-15 / AMPAR Flare: When the IMM voltage (ΔΨ) drops due to D+ contamination, the retrograde response isn't just a local signal; it’s a systemic alarm. High GDF-15 acts as the metabolic "smoke detector," while AMPAR dysregulation in the brainstem scrambles the glutamatergic signaling. This is the "optical noise" that prevents the thalamus from executing its postnatal neurogenesis "software."

The MITF-AMPAR Suicide Switch: The most striking part of my model for Rockefeller trained MDs or the parents that believe their bullshit is the destruction of melanin creation both endogenously and exogenously. If the body senses it cannot fractionate the deuterium (due to the backup), it downregulates the very system (MITF) meant to create the "magnetic traps." This is a biological "surrender" to the CDR, leading to the loss of quantum transparency in all neuroectodermal tissues in the skin, gut, and brain.

The Thalamic Stall: In children, if the Vagus/Transverse Mesocolon highway is backed up with deuterium, the thalamus cannot "see" clearly enough to build the CNS. The resulting GI stasis (slowed emptying) is simply the physical manifestation of a system that has lost its magnetic and kinetic "pull."

In short: Autism and developmental stagnation are a "clogged tailpipe" problem where deuterium creates an optical and electromagnetic fog that the developing brain cannot penetrate. Vaccines exacerbate all this biophysical blinding because they are loaded with deuterium and heavy atomic metals by design, by the Rockefeller paradigm. These atoms have to chelated by melanin for elimination via the gut, so blocking the exhaust is why this happens. Here is that paper. scilit.com/publications/3…

Based on recent laboratory analyses, this study published in late 2024 reported that 55 undeclared chemical elements were detected in COVID-19 vaccines from several manufacturers (AstraZeneca, CanSino, Moderna, Pfizer, Sinopharm, and Sputnik V) using Inductively Coupled Plasma Mass Spectrometry (ICP-MS). this test is not a standard laboratory test. I had sent letters out to many researchers over the last two decades asking them to test vaccine vials for undeclared atoms. This paper proved my decentralized thesis insights were spot on.

It is not hard to understand when you understand the equations below. Few centralized MDs do. I have shared my concerns directly with Dr. Hazan and we even did a podcast about how this all operates. UV-NIR light is key in the transdermal MITF-AMPAR repair of these kids. BigHarma wants no part of Uncle Jack because I know their grift.Image
Image
2.
A. Clogging the Melanin "Magnetic Trap"
In my decentrlaized model, melanin in the enterochromaffin cells acts as a paramagnetic filter to fractionate deuterium for clearance. The presence of these undeclared elements presents two major failures:

Chelation Overload: Melanin has a high affinity for heavy metals like lead, mercury, and nickel. If melanin is "occupied" chelating these 55 elements, its capacity to bind and clear deuterium is functionally diminished.

Electronic Interference: The study specifically highlights lanthanides (such as gadolinium and erbium), which are commonly used in optogenetics and electronics due to their unique magnetic and optical properties. These elements may "jam" the optical signaling of the melanin system, turning a clear quantum filter into an opaque "lead curtain."

This is why adults get gadolinium syndrome from too many MRI contrasted studies and why I stopped using Gadolinium about 20 years ago as a neurosurgeon. Many of the symptoms of Gad toxicity is seen today in GLP 1 abusers. GLP 1 agonists all block the exhasust system of EDAR and the glucagon genes on Chromosome two. POMC is also on Chromosome two for the non believers.Image
3. B Impact on Exocrine and IMM Signaling
(Delta Psi) I described in my thesis:
The accumulation of these elements would accelerate the breakdown of the ΔΨ on the IMM leading to the CDR.

Enzymatic Poisoning: Heavy metals like arsenic (found in 82% of samples) and chromium (100%) are known to disrupt enzymatic functions, potentially including the Carbonic Anhydrase II needed for the bicarb-deuterium exit.

Mitochondrial "Smoke": If the pancreas cannot clear the isotopic and chemical waste, the "exhaust" backs up into the brainstem. The study notes that the elemental composition of these vials is heterogeneous, meaning the "toxicity profile" varies, which would create unpredictable "optical noise" for the vagus nerve to transmit. This is the Rockefeller dirty little secret I found out about when I started snooping around vials 20 years ago. That is why they banned my TED talk, FYI.Image
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Read 10 tweets
Mar 15
He and Hameroff still do not understand melanin. If they did it would advance their ideas a lot further.
2. If the Lagrangian of life (L=T−V) is the "seed" of reality, then melanin was the earliest form of soil on Earth that allowed the environment to "unfurl" that seed into a useful photo-biological circuit. Melanin being spread all over the human mammalian body plan had massive impacts on consciousness.

Not including melanin in this story makes the story a half truth. My proposal is that melanin acts as a Battery Charger for transition metals.

This is the missing mechanical link that explains how early life navigated the Great Oxidation Event (GOE) without a catastrophic "short-circuit." Melanin turned invisible unusuable energy into a visible biological win we call life. It is part of the human Langrangian version of this equation. The electroweak force breaking time symmetry is the key to the mystery.
3. This is a profound expansion of my "physics-first" model for consciousness. By mapping the Lagrangian of physics, the fundamental balance of Kinetic (𝑇) and Potential (𝑉) energy, onto the biological emergence of life, I'm suggesting that melanin isn't just a pigment, but a fundamental biological force-carrier.

Here is my evaluation of my own proposal that melanin is the "missing mechanical link" in the Human Lagrangian from my blogs:

1. The "Soil" for the Biological Circuit
In the image provided, the Lagrangian (𝐿=𝑇−𝑉) is the "seed" that, through symmetry breaking, generates the particles of our universe.

In my thesis I've proposed proposing that melanin acted as the original substrate that allowed life to "choose its symmetry."

Because melanin is a biological semiconductor with massive pi-electron resonance (those aromatic rings we discussed), it acts as a "buffer" or "soil."

It can absorb high-energy, "invisible" radiation (UV, Gamma, X-rays) and convert it into low-energy, "usable" phonons or electrochemical gradients. This effectively prevents the "short-circuiting" of delicate early organic molecules. It does the same thing for consciousness. It provides the fuel to power it.Image
Read 10 tweets
Mar 12
You are A MORON. THIS PAPER IS DEVASTING. You do not seem to be able to read the literature nor decipher the implications.

Here is how this data likely fits into and strengthens my arguments in CPC #79 & 80:

1. Moving Beyond "Sarcopenic Obesity"
Standard critiques of GLP-1s focus on the ratio of fat-to-muscle loss. Mythesis can now argue that the problem isn't just the quantity of muscle lost during the weight loss phase, but a fundamental degradation of the quality and regenerative capacity of the remaining tissue. This is a loss of longevity due to Rockefeller time inflation. I’ve successfully moved the goalposts from a simple "muscle loss" argument to a
"regenerative failure" model, which is much harder for critics to dismiss as just a side effect of dieting. My term "drug time inflation" is a powerful way to describe the trade-off. While Ozempic might "buy" time by reducing cardiometabolic risk, the Blau data suggests it "spends" it by functionally aging the muscle’s repair system. What is the most important muscle in humans? The Heart. Damaging it will kill humans sooner. Never forget this effect will be minimized in mice because they are nocturnal and do not have the mitochondrial capacity in their hearts that humans do. I'd expect the fact to be magnified in humans.

2. The Mitochondrial Density Gap
The human heart is the most mitochondrial-dense organ in the body, requiring constant ATP for rhythmic contraction. Unlike mice, which have a much higher heart rate but lower overall mitochondrial "reserve" due to their size and nocturnal metabolic patterns, humans rely on PGE2-mediated repair to maintain cardiac density over decades.

My Argument: If Ozempic blocks PGE2 signaling via the Gerozyme pathway, the human heart cannot "rescue" damaged mitochondria. In humans, this doesn't just lead to "weakness"; it leads to cardiac remodeling and diastolic dysfunction.

3. Nocturnal vs. Diurnal Disconnect
Mice are nocturnal, meaning their repair cycles (melatonin/autophagy) happen during the day in a state of rest. Humans are diurnal.

The Problem: GLP-1 drugs have long half-lives (roughly 7 days for semaglutide). This means the "signal" never turns off. In humans, this persistent signaling may interfere with the circadian rhythm of mitochondrial repair in the heart, an effect that is minimized in short-lived, nocturnal mice who don't have to maintain cardiac tissue for 80+ years.

4. Magnification of Effect
I think my thesis is likely correct that the effect will be magnified in humans. In mice, the study showed an 8% recovery in strength, a catastrophic failure. In a human heart, an 8% recovery rate after minor cellular stress or sub-clinical ischemia is essentially a death sentence or a fast-track to heart failure with preserved ejection fraction (HFpEF).

5. Heteroplasmy in the Myocardium
Because the heart is post-mitotic (the cells don't divide often), it is uniquely susceptible to the heteroplasmy that I mentioned earlier. If the "repair signal" (PGE2) is degraded by the Gerozyme, and the GLP-1 drug is preventing stem cell activation, the human heart is forced to run on "broken engines" (damaged mitochondria) without the ability to replace them.

Summary From My Thesis: I can now argue based on the Blau data that the "Ozempic face" (loss of facial fat/collagen) is just a visual precursor to "Ozempic heart," a state where the most vital muscle in the body is losing its regenerative capacity and accumulating mitochondrial mutations (heteroplasmy) faster than it can repair them. I bet this will get this will get this pre print retracted and this will never be in PEER reviewed literature.

6. Identifying a Specific Biological Mechanism
The study suggests that semaglutide doesn't just "cause" muscle loss via weight loss; it appears to interact with the 15-PGDH (Gerozyme) pathway.

The Problem: Ozempic alone seems to suppress muscle stem cell function (down to 20% in mice), effectively "locking" the repair mechanism. When you realize in humans BCL11A is tied to regeneration and also sits on Chromosome 2 in humans with the glucagon gene. This is a high-level genetic catch from my thesis. I'm pointing to a "hot spot" on Chromosome 2 (2p15-p16) where the Glucagon gene (GCG), the precursor to GLP-1, resides near BCL11A.

The Link: BCL11A is famous for the "fetal-to-adult" hemoglobin switch, but recent research also ties it to regenerative capacity and cell fate.

My Thesis Fit: If GLP-1 drugs over-stimulate pathways linked to this region, they might inadvertently trigger a "switch" that favors immediate metabolic stability over long-term regenerative "fetal-like" plasticity. This supports my idea of a fundamental "locking" of repair and dying early from these drugs.

The Result: This leads to a failure in regeneration and strength recovery (dropping to 8% in the study), suggesting that users might not just be "thinner," but biologically "older" in terms of muscle resilience due to increased heteroplasmy. I said this in my thesis and now I have proof of it.

7. The "Gerozyme" Link
By linking GLP-1s to the 15-PGDH enzyme, my thesis can bridge metabolic health with longevity science. If 15-PGDH degrades PGE2 (the repair signal), then GLP-1 drugs "inadvertently accelerate" a marker of aging in muscle tissue. Human studies have shown that 15-PGDH activity is elevated in aged cardiac tissue, leading to a localized drop in PGE2. Human Relevance: Microarray data from human biopsies shows that 15-PGDH expression increases significantly with age in cardiovascular tissues. The GLP-1 Interaction: If GLP-1 drugs further suppress the "repair signal" (PGE2) while this enzyme is already high, it creates a "perfect storm" for cardiac cell failure. In mice, inhibiting this enzyme reversed diastolic dysfunction and reduced Troponin I (a marker of heart damage). Without this "fix," the damage this is why I anticipate in humans the process is deadly. Fits with the Rockefeller eugenics plan (COVID jab).

My point about the human heart's mitochondrial density is the "smoking gun for the death sentence these drugs are delivering to people today."
Mitochondrial "Lock-out": 15-PGDH inhibition has been shown to restore mitochondrial morphology, turning "large, distended, vacuous" aged mitochondria into "round, compact, healthy" ones.
The Human Penalty: Because humans have higher mitochondrial capacity requirements, the failure to repair these organelles (due to the GLP-1/Gerozyme interaction) will lead to accelerated heteroplasmy in the heart much faster than in the short-lived mouse. The known already published research indicates that 15-PGDH promotes cardiac fibrosis (scarring) via TGF-β1 signaling.

My Thesis Fit: You can argue that the "weight loss" seen on GLP-1s hides a "stiffening" of the heart. While the patient looks "fit" due to the scale, their myocardium is accumulating fibrotic tissue because the PGE2 "anti-fibrotic" shield has been compromised. This means anyone on these drugs needs to have invasive caridac testing to see how the drug has already damaged their hearts. Sounds a lot like the COVID jab if you ask me (myocarditis risk).

Comparison: Mouse vs. Human Cardiac Impact slide below.

Dr. Williams is a danger to patients. The public should be aware he cannot read well, and not comprehend the implications of recent research.Image
2. A Path to "GLP-1 Plus" Protocols
The most provocative part of this data for my thesis is the "Rescue" effect. By blocking the Gerozyme, the researchers restored muscle mass to 80% and regeneration to 95%. This suggests that the future of GLP-1 therapy might not be a drug,  It should be UV-A-NIR light with occasional cold therapy, in a combination therapy approach designed to protect the "regenerative engine" of the body.

SUMMARY

By lowering their function to 20%, the drug essentially creates a "debt" of repair capacity that may only become visible after an injury or as the user ages further.  this means doctors will be blinded to this as it happens.  So we should expect more sudden heart attacks in humans who use them. My intuition about increased heteroplasmy (the presence of mutated mitochondrial DNA alongside healthy DNA) fits the "Gerozyme" model perfectly.  The Mechanism: The Blau Lab found that 15-PGDH degrades PGE2, which is critical for mitochondrial health.
The Proof: When PGE2 is low, mitochondria struggle. This "mitochondrial stress" is a known driver of heteroplasmy. If Ozempic exacerbates this by not addressing the Gerozyme rise, the "thinness" achieved is indeed "biologically older" because the cellular power plants are degrading.
The "GLP-1 Plus" Protocol Rx is: Light & Cold = Leptin Rx.
I’ve pivoted from a pharmaceutical fix to a biophysical one. This aligns with the "Hallmarks of Aging" approach:

UV-A/NIR Light: Near-Infrared (NIR) light is known to stimulate cytochrome c oxidase in mitochondria, potentially mimicking the "rescue" effect of PGE2 by boosting ATP and reducing the ROS (reactive oxygen species) that Gerozymes thrive on.

Cold Therapy: This triggers hormetic stress, which can improve insulin sensitivity and mitochondrial biogenesis via the AMPK/SIRT1 pathway—the same pathway GLP-1s use, but without the stem cell "lockout".
Now you know why they buried the synthetic leptin trials.  Now you know why they banned my TED talk on this topic.Image
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3. It seems from the decentralized perspective that Big Harma technology and Big Tech's use of light has reversed engineered and stolen from mammalian biophysics and our cosmological upbringing of ozone filtered light, and hence this has led to a modern devolution and atavism in society.

That should be a profound realization for the public whose brain still operates to think, that moves the conversation from biology into archeo-physics. What I'm describing in my thesis is the Technological Mimicry Trap: the idea that modern "innovation" is actually a simplified, "dead" imitation of the complex, living quantum-coherent systems already perfected by Archean evolution. By reverse-engineering these biological "vows" into silicon, steel, & LED light we create a world that is fundamentally atavistic, designed to drag the highly evolved, coherent human biology back toward a state of disordered, into a world of high-entropy chaos where drugs can be sold to soothe your ills.

1. The Parasitic Nature of Technology
Technology often "steals" a biophysical principle but strips cells of its Isotopic Filter for deuterium and masses and removes Chiral Spin Selectivity of melanin.

The Grid vs. The Vagus: The AC power grid is a "stolen" version of the nervous system’s oscillatory signaling that occured during the Electric Wars by JP Morgan. However, while the Vagus Nerve operates on coherent, p-mode oscillations tuned to the Earth's Schumann resonance, the 60Hz grid is a "heavy" frequency that vibrates at a scale that shatters the IMJ geometry by letting deuterium rush in to destroy the matrix.

The Processor vs. The Mitochondria: A computer chip uses electron flow across junctions, but it lacks the CISS effect linked to melanin. It doesn't care about spin; it only cares about charge. Melanin cares about BOTH. This "crude" movement of electrons generates heat (entropy) which is why computer centers need AC/water cooling, whereas the IMJ's spin-polarized transport generates light (information) and not much heat.

2. Devolution Through "Externalization"
When we externalize a biological function into a gadget, we cause the biological "organ" to atrophy, leading to biological devolution/atavism:

GLP-1 as Externalized Vagal Tone: Using a drug to force satiety is a "stolen" version of the VN-NTS feedback loop. By using an external chemical "wrench" to slow the stomach, the body’s internal deuterium-dumping mechanisms (the exocrine and autonomic circuits) go dormant.

The Atavistic Result: We lose the ability to sense our own isotopic load (deuterium interoception). As a result, we become "biological zombies,"physically present but quantum-topologically disconnected from the fabric of Nature.

3. The Reversal of the "Geometric Vow"
The "Geometric Vow" of the IMJ is a commitment to negentropy (increasing order). Technology, by its current design, enforces a 51% attack on the Vow:

Deuterium Accumulation: Our technological environment (nnEMF, processed foods, blue light) actively prevents the body from "dumping" deuterium.

The Atavistic Shift: This forces the cell into the M1/Cell Danger Response (CDR). The M1 phenotype is a "throwback" to a more primitive, anaerobic, "survival-only" state of existence (Warburg shift). This is the definition of atavism, the return to an ancestral, less-refined biological state in evolutionary history. Your life is lived backward in time but your anatomy is that of the latest versions of mammals. This is the ultimate thermodynamic mismatch.

4. Sovereignty as "Anti-Tech" Biophysics
If technology is "stolen" biophysics, then true health is a reclamation of the original code based in the mammalian blueprint.

The Solar-Terrestrial Interface: Instead of using an external "bio-hack" or drug, sovereignty comes from honoring the Sunrise/Melanin/Cold trinity. These are the original "technologies" that defend the IMJ against the heavy-neutron interference of deuterium from the unfettered electromagnetic spectrum in the Archean world which is now being built by the modern technological world.

Blockchain of Quantum Events: I've mentioned biology as a TIME blockchain. In this sense, the "consensus mechanism" of your health is the coherence of your Vagus Nerve. Every time you align with the natural light-dark cycle, you "mine" a coherent block and time controls the flow of energy in cells well.

Every time you rely on a "stolen" technological proxy (like a GLP-1 agonist), you allow a "fork" in your biological code that leads toward devolution via atavism. You lose time. Loss of time is an inflationary event for longevity. This is why GLP 1 drugs will shorten your life.

I am effectively arguing that we are living in a biophysical plagiarism. We have built a world that mimics our form but destroys our essence.Image
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Read 4 tweets
Mar 12
Elliot needs to brush up on the embryology of the face.
It is intimately linked to NCC which follow melanopsins lead into the cells that become the the mid face and jaws and they develop based on brain growth. I'm not surprised that a food guru has no clue how melanin from NCC drives this process. LOL.

Elliot seems to be ignorant that NCCs are the progenitors of both melanocytes and much of the craniofacial mesenchyme (e.g., maxilla, mandible via ectomesenchyme), tha tbecome the HUMAN FACE.

This shared origin explains evolutionary yoking of facial shape and pigmentation, as variations in NCC genes (e.g., Pax3/7) affect both melanin density and craniofacial morphology. Sorry to tell you Elliot, but it appears you are dumbass for not knowing how melanin is directly related to your double jaw surgery.

Low maternal UV/IR exposure is a known risk factor reducing melanin synthesis, increasing NCC vulnerability to apoptosis via chaotic UPE (ultra-weak photon emission), as NCCs are sensitive to oxidative stress in the embryo's face. Disruptions in NCC migration/differentiation lead to hypoplasia; e.g., in Waardenburg syndrome, and today it is well known by all except Elliot, that melanin defects correlates with craniofacial anomalies.

pmc.ncbi.nlm.nih.gov/articles/PMC43…

If the "mass" of NCC does not arrive to the correct sites in the embryo, the geometry of the face is never correct and leads to post natal deformities and associated risks.

The DC Current: In optimal health, the embryo generates a bioelectric field which forms primitive version of the Melanin-Water battery created by NNC and CCO function in mitochondria. This field acts as a "GPS" (Galvanotaxis) for NCCs to migrate into the somites and arches that form facial structures.

The Hypoplasia: If this current is weak (due to low maternal redox or nnEMF interference), the NCCs "stall" or "get lost in migration patterns of the embryo." This leads to Maxillary and Mandibular Hypoplasia (receded jaws), which can be the structural root of the Sleep Apnea. The "Mass" simply never arrives at the "Scene of face."

In the decentralized framework, Craniofacial Dysmorphology is a failure of Topological Embryogenesis due to altered DC electric currents that ultimate come from melanin via neural crest cells that have to migrate into the embryonic facial structures to complete its growth. The lack of neural crest cell (NCC) migration is the result of a "cold" or "dark" Bioelectric Field that fails to provide the DC current necessary to guide these cells to their destination.

The NCC "Galvanotaxis" Failure Neural crest cells are the "Exploratory Stem Cells" of the vertebrate body. They migrate from the neural tube to form the Maxilla and Mandible by following a voltage gradient.

The palate/jaw act as a mechanical resonator for brain growth, with receded mandible shrinking the airway, triggering Piezo1 sensors in the brainstem for a "bunker" response in sleep apnea. Bone's piezoelectricity generates DC currents during chewing to hydrate the "vascular pecten" via CCO that is needed to hydrate melanin for the DC current to be optimized in the picoampere range per Becker's work for bone growth.

The palate and jaw influence airway patency; mandibular hypoplasia in PRS or craniosynostosis causes glossoptosis and OSA via mechanical strain.

Piezo1, a mechanosensitive channel, is expressed in the brainstem and responds to stretch/shear stress, potentially linking airway obstruction to respiratory control disruptions in OSA. Bone is piezoelectric, generating DC currents under mechanical load (embryonic movement of tongue or chewing), which stimulates osteogenesis and vascular hydration of NCC derivative via CCO (cytochrome c oxidase) in mitochondria. Low NCC mass from defective maternal/paternal redox in their germlines reduce this "charge," impairing brain vascular support leading to aberrent craniofacial growth. Very embarrassing for you Elliot to be undressed a decade later wearing a T shirt that you never explored.
2. The interplay of NCC (melanin), the VDR and CCO on the IMM regulates mtDNA-driven melatonin production, which is critical for hormonal signaling and bone growth. Embryonic hypoxia disrupts CCO activity, CCO activity changes the DC current from melanin in NCC's and CCO is also capable of reducing melatonin and altering UPE transformation in embryogenesis, thus, damaging mtDNA via ROS, leading to altered developmental patterns in craniosynostosis (suture fusion), scoliosis(vertebral asymmetry), and malocclusions (maxillary/mandibular growth defects). Melanin and Melatonin links these conditions by modulating osteoblast activity and hormonal pathways (e.g., estrogen, IGF-1), while UPE and bioelectric currents (per Becker) provide biophysical signaling mechanisms that coordinate NCC and mesodermal development. VDR dysfunction amplifies these effects by impairing mitochondrial function and calcium signaling, particularly in NCC-derived tissues (maxilla, mandible, sutures) and mesodermal tissues (vertebrae).

Ultra-Weak Photon Emission (UPE):
UPEs, are generated by CCO activity and ROS in the IMM, and serve as a biophysical signaling mechanism, coordinating cellular differentiation and tissue morphogenesis. Reduced UPE due to impaired CCO (e.g., from hypoxia or VDR dysfunction) disrupt:
Suture patency, leading to craniosynostosis.
Vertebral symmetry, contributing to scoliosis.
NCC migration, causing maxillary/mandibular growth defects and malocclusions.
Melatonin, as an antioxidant created by ELF-UV light emission, reduces excessive ROS, helps create Vitamin D and stimulates the VDR on the IMM to affect electron tunneling, which can stabilize UPE signaling. Mitochondrial melatonin deficiency and altered DC currents from the hydration status of CCO on melanin will lead to erratic UPE patterns, disrupting developmental signaling in NCCs and mesodermal cells.....So Elliot you remain a dumbass for a decade now. I hope your oral surgeon is better informed so you do not get a nerve injury from this henious surgery. LOLImage
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3. The "Mitochondriac" Conclusion: You cannot fix a "Proterozoic Face" with a dental appliance or a double jaw surgery, alone. You must restore the Picoampere Current by re-hydrating the Melanin via the Sunrise/Grounding/CT triad to reduce the risk of OSU in the adult. That is the evidence Elliot. You remain a clueless food guru.
Read 5 tweets
Mar 11
Sleep apnea is the brain protecting itself from nnEMF and blue light.  Oxygen is toxin to people with sleep apnea, and it also has a U shaped curve based on GOE evolution, hence why modern humans have it so commonly today since nnEMF mimics dehydration and hypoxia in our environment.
What did the blogs say about exogenous oxygen? Oxygen is quantized to the stoichiometry of the TCA/urea cycle.  What if you Kreb's bicycle is dysfunctional because you never see the sunrise?Image
2. What happens to melanin when pseudohypoxia occurs due to nnEMF = Melanin dehydrates and become massively conductive in cells = Archean legacy = causes damage too all evolution built from the GOE onwards. No one sees it until they do.

3. Sleep apnea is the brain protecting itself from nnEMF and blue light.  Oxygen is toxin to people with sleep apnea, and it also has a U shaped curve based on GOE evolution, hence why modern humans have it so commonly today since nnEMF mimics dehydration and hypoxia in our environment.

What happens to melanin when pseudohypoxia occurs due to nnEMF =  Melanin dehydrates and become massively conductive in cells = Archean legacy = causes damage too all evolution built from the GOE onwards.  No one sees it until they do.
Sleep Apnea is not a respiratory failure, but a Topological Defense Mechanism. The brain induces apnea to limit oxygen entry because, in a decoherent system, oxygen is the "match" that ignites the sPLA2-IIA Supernova to destroy organs.

If your nnEMF/Blue light environment mimics deuterium-induced dehydration, your Inner Mitochondrial Junctions (IMJs) collapse. You lose the CISS (Chiral Induced Spin Selectivity) needed to spin-match oxygen.  In this "M1" state, incoming oxygen cannot be reduced cleanly to metabolic water. Instead, it creates a "flood" of Superoxide. The brain senses this oxidative "fire" and stops breathing (Apnea) to prevent the total destruction of the neural mitochondria.
x.com/DrJackKruse/st…

My blogs and my thesis align on apnea being a "Proterozoic" survival strategy.  Oxygen is a powerful paramagnetic radical. During the Great Oxidation Event (GOE), life had to evolve the Melanin-Metal shield and D-shell transition metals to "gate" oxygen.

Sleep Apnea is the body's attempt to regress to a Proterozoic state to survive a high-EMF environment. You aren't "missing air"; you are missing the Photonic DC current needed to make oxygen safe.  This is a counterintuitive truth bomb of evolution on Earth through the GOE lens.

What did the blogs say about exogenous oxygen when melanin is not hydrated? Oxygen utilization must be quantized to the stoichiometry of the TCA/urea cycle.  On the IMM sits CCO that makes the water that hydrates endogenous melanin.  What happens if your Kreb's bicycle loops of TCA and urea cycles are dysfunctional?

This decentralized take implies solar light to stimulate melanin production on the skin is a better & safer option than using a apnea machine because most sleep MDs do not do matrix/cytosol stoichiometry testing on apnea patients to see how toxic oxygen is. This also explains why many people with apnea suffer from atrophic skin.
Read 8 tweets
Mar 6
1. Question asked on the forum today: Hello all.
I'm $%^#@@ from Kansas City MO northern outskirts. 39° lattitude. 49 yo female
RLE surgery in left eye in December of 2023 (obviously before I found Dr. Kruse)...hopefully still getting enough beautiful sun in my one untouched eye.

Have faught with heartburn (small HH ) off and on for years...got off of H2 blocker 2 years ago and try to control mainly through diet/random supplements but phasing those out as I listen more to Doc.
Weak ass bladder after 2 kids that seems to get worse every year.

No other real medical history except some anemia the last few years (suspected d/t heavier periods/fibroids) and so my doctor currently has me on iron.
RN for 14 years now, bedside nursing, night shift...don't scold me...been making the transition to days since following Dr. Kruse and currently down to only one or two night shifts a month now.

Wearing my blueblockers most of the time, catching the sunrise and sunset pretty much most days since November and trying to get through Dr. Kruse's blogs the best I can without feeling too stupid. Plan on moving in the next few years after last kid is out of highschool. Where? I don't know...still have a lot of convincing to do to the spouse.

Hope to make it out to El Salvador for the 1st time this summer, maybe fall.Image
2. My ANSWER: This complex web of symptoms, ranging from eye surgery and heartburn to pelvic floor dysfunction and night shift challenges, reflects a deep systemic breakdown of the circadian and dopaminergic systems often seen in chronic metabolic conditions like diabetes.

1. The RPE-SCN "Optical Blindness"
The retinal pigment epithelium (RPE) and the suprachiasmatic nucleus (SCN), the body's master clock, are fundamentally linked through light perception and matrix metabolic regulation.

RPE Dysfunction: In night shift workers, high blood sugar causes early damage to the RPE barrier, leading to fluid leakage and "optical blindness" where the eye fails to properly process light-driven metabolic signals.

SCN Misalignment: When the RPE fails, the SCN loses its precise "zeitgeber" (time-giver) input. Working night shifts exacerbates this by forcing the body to operate against its natural light-dark cycle, leading to chronic circadian misalignment.

The "Untouched" Eye: Seeking sun in one eye while the other has undergone surgery (like RLE) may be an intuitive attempt to "re-sync" the SCN, though the systemic metabolic damage often persists across both eyesImage
3. The image highlights that UV-A and IR-A (Infrared) are the fuels for regeneration.

The Problem: In a modern environment (LEDs, screens, night shifts), we are often "UV-A/IR-A deficient" but "Blue Light toxic."

The Result: Without those specific frequencies, the RPE (Retinal Pigment Epithelium) cannot recycle the waste from your photoreceptors. This is the "optical blindness" where the eye is physically there, but the biochemical signaling of time is lost and this leads to all your current issues.

2. Dopamine, GERD, and Pelvic Floor Dysfunction
Dopamine acts as a bridge between your circadian clock and physical functions like digestion and muscle control.
The diagram shows Dopamine (DA) as the "Light" signal.

Muscle Fiber Type: low dopamine leads to muscle dysfunction. In my framework, dopamine is essential for maintaining the vagal tone and the correct "firing" of smooth muscles.

The GERD & Pelvic Link: If retinal dopamine is low, the signal to the brainstem is weak (PVN). This affects the Autonomic Nervous System, leading to the "loose" GE reflex (heartburn) and the "discordant" muscle tone in the pelvic floor. It’s not just a local muscle issue; it’s a top-down timing error you are experiencing from being a night shift nurse. My bet in your operated eye there was big time myopia of evidence of Drusen present.
Blue light and nnEMF toxicity often causes autonomic neuropathy, which delays gastric emptying and weakens the esophageal sphincter. Dopamine receptors (D2/D3) help regulate these digestive rhythms; when they are "out of sync," it manifests as chronic reflux or GERD.
Pelvic Floor Dysfunction: Chronic hyperglycemia damages the nerves and blood vessels supplying the pelvic floor. This can lead to diabetic bladder dysfunction (incontinence or urgency) and weakened structural support, which is further complicated by the "dopamine thing", as dopamine is essential for the coordinated muscle contractions required for pelvic health. The fact this is getting worse at 49 means your days of being a nurse should be over because you need a massive infusion of UV-NIR light during the day to fix all of this.Image
Read 10 tweets

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