@DrJackKruse: Pretty cool zionist story. I can top it.
TODAY’s PSA only my decentralized MDs know because of our private lessons.
What does POMC, eccrine glands, exocrine gland evolution have in common?
All of them are found human chromosome two. Why is this unusual?
What if I told you this is why Rockefeller Medicine had my Ted talk banned 15 years ago?
I knew they were going to destroy the science around leptin when they cancelled the trials and did three things in their patents.
-
Patented cold receptors.
-
Made sure Monsanto was sold to Bayer
-
Used computer modeling to create drugs that would target exocrine biology
-
Patent drug targets of the TIM circadian clock gene.
Did you know the target of GLP 1 agonist are also on Chromosome 2 and BigPharma was shitting the bed 15 years ago that I was going to let their secret new target out of the bag. So they tried to cancel me like they did to Andy Wakefield.
I LOL’ed
The fusion of ancestral ape chromosomes into human Chromosome 2 (6–7 Ma) was the ultimate “Hard Fork” in the mammalian ledger. Keeping POMC on the p arm of this massive new chromosome placed the “Light-Integration” instructions in a prime “real estate” zone for the expanding neocortex. This gorilla duplication and fusion event provided the genomic stability to support a higher hashing power (increased mitochondrial density in neurons). It allowed the human brain to “mine” more complex time-percepts than any gorilla or chimp, simply because the POMC-Melanin-Mitochondrial relay was now hardwired adjacent to the mitochondrial matrix into the core of our newest genetic hardware. Essentially this was a consensus shift for the human blockchain. It means humans could sense light and temperature changes from their skin and bring that info directly to the mitochondria without ever needing to translate one nuclear gene to change the mammalian body plan. This is why the Human and Gorilla Genome shocked the world in the Clinton years. Humans did not need extra genes because the entire program sits on chromosome number two for the leptin melanocortin pathway. Extra genes would have costed energy and more energy would have meant less brain. Using light the TIM clock gene humans were able to use the extra energy to expand their cortex fast.
The HGP Truth: As the Human Genome Project hinted, the 20,000 genes are just the “parts.” The UPE maps (Light/EMF) are the “Assembly Instructions.”
The Human Advantage: Our Chromosome 2 fusion gave us the “bandwidth” to run the most advanced Optical Logic Gate on Earth.
The Shift: By bringing melanin “inside” and stabilizing its control via the POMC-Integrator on Chromosome 2, humans shifted the “Operating System” from the Nucleus to the Melanin-Mitochondrial Syncytium.
Wireless Regulation: Melanin and the water matrix act as a broadband semiconductor. They process light and electromagnetic fields to regulate the cell at the femto and atto timescales. This “Wireless” regulation bypasses the need for 100,000 different “hardwired” gene sequences. We didn’t need more genes; we needed a better transceiver.
As a result of this one change, human morphogenesis became expensive in timing, and not in energy. This allowed for massive encephalization. No gene expansion needed.
The skin Optical logic gate needed to be cooled to send pristine info inside to the matrix of trillions of cells. Chromosome 2 also controls the cooling program = 𝐸𝐷𝐴𝑅 built the “exhaust pipes” (eccrine glands), endogenous 𝑃𝑂𝑀𝐶 manages the “metabolic brake” and the light-driven signals from our surfaces that tell those pipes when to open. This is why the return of sweating is a big part of my Leptin Rx. I’ve noted in my decentralized thesis on Patreon, the explosion of eccrine glands in humans (via the EDAR/EN1 pathway on Chr 2) was not just about surviving the savanna, it was about Thermal Management of a Surface Semiconductor to send SUPERIOR light information to the interior to keep the nuclear genome quiet for energy efficiency.
What was the other system that Rockefeller medicine targeted after they cancelled the leptin trials? They knew I knew what they were really doing. While my earlier focus was on the p-arm (POMC), I found out in 2005 that the q-arm of Chromosome 2 (specifically 2q24.2) houses the GCG (Pre-proglucagon) gene. This was the smoking gun for their medical tyranny.
The GCG gene produces Glucagon, GLP-1, and GLP-2. These aren’t just for blood sugar; they regulate the growth, repair, and motility of the intestinal epithelium. GLP-1 agonists act as a “Quantum Jammer” that breaks the decentralized Chromosome 2 timing loop controlled by the TIM clock gene. Why do people using these drugs have to worry about the MEN syndromes side effects?
The thyroid is a key zip code for the TIM (Timeless) clock gene. By disrupting the light-mediated feedback of the SCN-Habenula-Thyroid axis, GLP-1 agonists force the C-cells to revert to the PaxB (Precambrian) genetic program = MEN Syndromic Cancers.
When the “centralized authorities” came to visit me after centralized powers cancelled my Ted talk they wanted to know what i knew. They were looking at my computer for any info on how I knew all this material. Remember the first GLP 1 was: Exenatide (Byetta) in 2005.
So where did I hide it? In the last place they’d look. I hid it in a Rockefeller bank in NYC. Recall leptin was discovered in 1994 in NYC at Rockefeller University. Now the world is getting that info on their medical tyranny. Every last bit of the drug creation of GLP-1A is tied to the MKULTRA program. GLP-1 receptors are highly expressed in the Retinal Pigment Epithelium (RPE). This is why GLP -1 agonist users are going blind.
I’ve now bridged the gap for my tribe between the Charity Hospital boxes, The Monk Who Sold his Ferrari, all the way to the modern GLP-1 craze in this blog. You might want to read it sometime —–> https://patreon.com/posts/cpc-78-nazi-150408576
What is the real MKULTRA story? Any patient on a GLP-1 agonist drug is like a star that is shedding its atmosphere to avoid a supernova. You’ve been warned. The genie is out of the bottle.
tweet source: https://x.com/TooWhiteToTweet/status/2022709503267844383
How fast can you get from a completely random, seemingly innocuous item in life to the most powerful and grotesque people in the world, like Jeffrey Epstein?
Let’s see:
New Hampshire eliminates vehicle inspections.
A Kentucky-based emissions equipment company sues NH, creating legal chaos.
The parent company, Searchlight Capital, is owned by Eric Zinterhofer, who is Jewish, and appears as a contact in the Epstein files.
His wife, Aerin Lauder, who is Jewish, is listed as a social contact in Epstein’s black book, with three phone numbers.
Her father, billionaire Ronald Lauder, appears in the Epstein files over 900 times, and was a known Epstein associate. He was involved in an art LLC with Epstein. Such art LLCs, of course, are notorious for being international money laundering operations. He is the president of the World Jewish Congress.
Just ponder for a moment how even the most obscure aspects of our daily lives are affected by the worst people on Earth.
There you are, deep in the no-man’s-land of New Hampshire’s great north woods, digging your car out of the snow, looking at the inspection sticker in your window, where, from there, you’re able to draw a very direct, very short line from that inspection sticker to the most notorious Jewish villain of our time.