1. Sunlight releases 250-780 nm light. 250-270 nm light is UVC light. Anything below this level is considered VUV light. The UV-C and VUV light is the light that scares physicians for only one reason. Big Pharma has convinced them that this causes direct DNA damage to human cells so it needs to be eliminated. I wonder what will happen when we build a photomultiplier that can measure the spectrum emitted from cells and find out that we create both UVC and VUV light?

IS THIS Big Pharma MEME TRUE about the toxicity of deep UV light? No, it is not. Why does it persist? Once humans harness the sun's frequencies in this area we won't have a lot of drugs in healthcare to treat a lot of diseases. The sun's light is a decentralized compound pharmacy for health. @RickRubin

This belief/perception is why light confusion exists and few studies are being done in vivo. Be aware of this. In summary, it has been known during the past one hundred years that UVC irradiation is highly bactericidal; however, using UVC illumination for the prevention and treatment of localized infections is still in the very early stages of development because of the influence of Big Pharma's profiteering. @hubermanlab

Most of the studies are limited to in vitro and ex vivo levels, while in vivo animal studies and clinical studies are much rarer. A major advantage of using UVC over antibiotics is that UVC can rapidly eradicate resistant and pathogenic microorganisms without any systemic side effects. UVC may also be much more cost-effective than the commonly used antibiotics. SHOCKER to no one except the centralized shills. @JuicefBukele
2. Centralized medicine born from Rockefeller has some good points, and is great in an acute emergency situation, but it’s high time people realized that today’s mainstream medicine (Western centralized medicine or allopathy or functional medicine), with its focus on drug supplements, drugs, radiation, drugs, surgery, drugs and more drugs, is at its foundation a money-spinning Rockefeller creation.
3. This thread will detail the bizarre history behind John D. Rockefeller's creation of centralized Big Pharma and the foundations of Western Medicine that are destroying our metabolic health. @JuicefBukele

John D. Rockefeller was an oil magnate and one of the richest men in history. He was America’s first billionaire and amassed a fortune of $498B adjusted for inflation of the USD as of 2023.
@JuicefBukele 4. Through monopolistic practices, Rockefeller grew his company, Standard Oil, to control 90% of all oil refineries in the U.S. Standard Oil has since broken up and has now become Chevron, Exxon, Mobil, etc. Yes, that’s how big Standard Oil was in its prime. Image
5. In 1900, Scientists discovered petrochemicals. These were chemicals that could be created from oil. Bakelite, the first plastic, was created from oil in 1907.

Scientists were discovering various synthetic vitamins that could be used to treat illnesses such as Scurvy and Rickets that were caused by Vitamin deficiencies. Rockefeller thought that Petrochemicals could also be used to create vitamins and medications.

Petrochemicals would allow Rockefeller to monopolize another industry in addition to oil. Business-wise, Rockefeller could patent these Petrochemicals and sell them for immense profits.

Rockefeller acted quickly and purchased part of I.G. Farben - a German manufacturing company. Side Note: I.G. Farben supplied the Nazis during WWII. Yep, look it up.

However, Rockefeller faced a major dilemma as he looked to monopolize medicine: Natural and herbal medicines were incredibly popular at the time due to the vitalists in medicine who were practicing the first version of decentralized medicine at the time. Many doctors and medical schools in the US were advocating practices born in NATURE as treatment & cures.

Like he did for other competing oil companies, Rockefeller viewed natural remedies as his "competition" that needed to be decimated. Rockefeller teamed up with Andrew Carnegie and hired a man named Abraham Flexner through the Carnegie Foundation to do just that. He decided to control the curriculum of all US medical schools to change the narrative with propaganda.
@JuicefBukele Flexner’s role was to travel the US and review Medical schools & hospitals across the country. This led to the Flexner Report which resulted in the closure of almost 50% of all medical schools. Image
7. Natural medicines, uses of electric and magnetic currents, and chiropractic care, were utterly decimated in the report. Some holistic doctors were even jailed. Rockefeller also donated a whopping $100M to colleges and hospitals under his philanthropic group called the General Education Board.

Flexner's report got us away from bioelectricity and toward the biochemical pathway before the discovery of DNA in 1953. This is when centralized medicine became an NGO of the Rockefeller foundation to ruin the health of North America. This was payback to Teddy Roosevelt. The goal was to bankrupt the US by creating a paradigm of sickness. Every American was now viewed as a customer in sick care. If you cured them the Rockefeller Foundation lost money through their Big Pharma subsidiaries. This is how Harvard, the Mayo Clinic, & Johns Hopkins came to dominate modern centralized medicine and policy. Nothing in this paradigm is evidence-based when you control the curriculum being TAUGHT and the research that gets funded and published as we saw in the pandemic era. The DNA discovery entrenched us in the Rockefeller paradigm of drugs over Nature.

In a short period of time, medical schools & hospitals were homogenized with the same approach. Their curricula became the first algorithm used in medicine to suit a profiteer. Medicine was just about patented drugs, not utilizing holistic & natural approaches as treatment.

Rockefeller's next step was to launch a smear campaign against his holistic "competitors." Homeopathy and Natural Medicines were quickly discredited by the newspapers and media outlets. He used the media as his propaganda machine to create Big Pharma.
8. Rockefeller's approach worked incredibly well as he decimated the decentralized competition in healthcare and ultimately created our current centralized medical system. This system continues today: Big Pharma makes large donations to medical schools in exchange for these schools to prescribe their drugs. They also buy most of the ads on media and these are their current marketing arms to push narratives they want pushed into your consciousness. This is why people think these tertiary care centers of excellent are good places........... They are sausage factories for patients' tissues and lives.

Again, this post is not to bash Western centralized Medicine. It is to spread SUNSHINE on show the unfiltered history of John D. Rockefeller and the role he played in shaping our current centralized healthcare system.
9. The next time your CENTRALIZED doctor spends 3 minutes with you during your visit and you feel like a "customer" instead of a patient and you get handed an Rx for all your ills and complaints, this post will hopefully give you clarity on why it is happening.

Not surprisingly, the cost of medical care in the US is #1 in the world, yet our quality is ranked at #37. Yet, some people I have recently met thought that following the Tertiary care centers pathways in healthcare were WISE?

Some bridges need to be burned down so we never go down them again.
10. It is your responsibility to be the DECENTRALIZED CEO of your own health. At the end of the day, no one cares about your own health more than you. Take in a variety of different inputs and make the decision of what is in your best interest.

Food is the fuel of the mitochondrial engines. The Mitochondrial engines are quantum photomultipliers of food's electromagnetic bar code built by the sun and Earth's environments. Food changes as the sun varies and the environment on Earth changes.

Start seeing the sun and Earth's environment that determine how your engines operate.
Start seeing your food and lifestyle as a version of decentralized medicine. Be intentional about where you source your food and the amount of sun and darkness at night you get to improve the sleep you get. Use these as your pillars to THRIVE.

Just how good has the Mayo Clinic been for the Public Health

The ROI of centralized medicine in one chart.
11. Never Forget it was the Mayo Clinic, Harvard, and Johns Hopkins led the charge to this demise over the last three years. Remember what the mandate was pushing and who created it. Aftermarket data: A great deal of intelligence has been invested in the ignorance of modern centralized healthcare. We can now see that in the mRNA experiment done globally over the last two years. The Morbidity and Mortality conference of the actions of the players should get them all fired and thrown in jail.
12. Future centralized doctors are ill-prepared for a world of patients bathing in nnEMF that changes how organic chemistry operates in cells. Hire decentralized docs who aced organic chemistry and every other type of chemistry associated with the biophysics of life. I wonder if med school admissions departments will get the names of the premed students who signed this petition? It seems like an important piece of info when considering their fitness for medicine, no?
13. This is how centralized medicine PEER review is done, folks. If you can get a study to support your drug... you publish it. If the trial failed you disregard it. It's called publication bias. It sits at the deceit of the centralized system of medicine. When you consider the totality of the scientific evidence you quickly discover antidepressants are a placebo with horrible side effects & potential for serious adverse consequences. Unfortunately, most doctors are not even aware of this and with Google patrolling and changing how search is done, any non-suspecting person will just do a quick Google search & read a biased study claiming this drug works. Always question Big Pharma's claim of evidence.
14. In a very short time, Rockefeller obtained his goal of paying back the US gov't for breaking up his Oil empire. Medical colleges at the time were all streamlined and homogenized. All the students were learning the same thing, and medicine was all about using patented drugs from his new companies spun off in NJ from Standard Oil.
CENTRALIZED Scientists received huge grants to study how plants cured diseases, but their goal was to first identify which chemicals in the plant were effective, and then recreate a similar chemical – but not identical – in the lab that could be patented. This is how the shill PhD was born.
A pill for the ill became the mantra of modern centralized medicine.
No one has wrecked more damage to the public health than the Rockefeller Foundation.
So, now we are, 100 years later, churning out centralized doctors who know nothing about the benefits of nutrition or herbs or any Natural practices around light water and magnetism and mitochondrial DNA. We have an entire society that is enslaved to corporations for its well-being.
America spends 15% of its GDP on healthcare, which should be really called “sick care.” It is focused not on cure, but only on symptoms, thus creating repeat customers. There is no cure for cancer, diabetes, autism, asthma, or even flu.
Why would there be real cures? This is a system founded by oligarchs and plutocrats, not by doctors.
15. I'd heard a reference to sunlight containing Lithium via a song by Sting .... "Lithium Sunset"
When asked about the sun he said.....
“The idea for this song came to me when I was in Brazil, I have a great fondness for Brazil, and I met what I can best describe as a shaman (who happens to have a degree in Chemistry). He was explaining something to me, he was saying that sunlight is composed of a lot of elements and one of them is Lithium, as you know, Lithium is a medication given to the depressed, it’s a very successful drug. But it actually exists in sunlight and at sunrise and sunset you can look into the sun without damage the eye does not filter yellow light so the Lithium goes straight to the brain. This is why people get a great deal of comfort and solace from looking at the sunset or the sunrise. So I wrote a song called “Lithium Sunset” which is an ode to this natural medication that is available to all.”
Sting (422)
How can light contain Lithium doc ....?
This doesn't make sense. Dr. Kruse responds: Don all elements on the periodic table have a specific light frequency they emit and this is their light fingerprint. This fingerprint can travel 93 million miles to Earth to interact with chemicals that contain this element and it will react to this similar frequency via a vibration. We call this molecular resonance. I have written extensively about it in the blog and on my forum. You need to understand how this light fingerprint can be used to activate Lithium in your brain to change your mood. That is how all elements and all bio-molecules work. We've been conditioned to believe it is a lock and key mechanism but this is a very simplistic linear way of thinking about chemistry. Light controls all chemicals by imparting information and energy to their valence electrons and once the light frequency matches the element or chemical the distant element or chemical reacts. This is how sunlight can affect a depressed brain. It turns out lithium light from the sun is more abundant in AM and sunset light so Sting was right about his song. In fact, he used this to stimulate his own creativity when he had writer's block in his career. So let me give you some deep basics about how this works in you......... Human skin's optical window is tight and is between 500nm -1000nm. 42 %-49% of sunlight is IR-A light. IR-A light has a wavelength of 0.75–1.4 µm IR-A frequencies range is 214–400 THz The electron volts of IR-A is 886–1653 meV and its temperature range is 3,864–2,070 K (3,591–1,797 °C)

The human eye cannot see it but these frequencies are present all the time when sunlight is present and this light innovates quantum solutions for living things. Each chemical bond in a molecule vibrates at a frequency characteristic of that bond. A group of atoms in a molecule (e.g., CH2) may have multiple modes of oscillation caused by the stretching and bending motions of the group as a whole. If an oscillation leads to a change in dipole in the molecule then it will absorb a photon that has the same frequency. The vibrational frequencies of most molecules correspond to the frequencies of infrared light. Infrared radiation is emitted or absorbed by molecules when they change their rotational-vibrational movements. It excites vibrational modes in a molecule through a change in the dipole moment, making it a useful frequency range for the study of these energy states for molecules of the proper symmetry. When hormones are altered so they can be patented these small changes alter their dipole moment and change chemistry in some small way but can have huge implications when this chemical interacts with light via the optical window of the skin. When you know better........you do better. This is DECENTRALAIZED MEDICINE.
16. When your melatonin/cortisol rhythm is off due to dark indoor days and bright artificially lit nights, not only are you affecting sleep and hormone levels, but you are also changing the size and shape of your mitochondria which changes your magnesium levels in the matrix and its hydration shell. This leads to energy inefficiency and age/disease acceleration. Did you know the size and shape of your hydration shell of magnesium is the ion lever that red light from the sun works on to change energy dynamics in the mitochondrial matrix? This is DECENTRALIZED MEDICINE.
17. We know that there are several exceptions in the standard genetic code for codons but over the 3.8 billion years of evolution, there is only one codon as methionine code for tryptophan. That is an extraordinary fact. It is as extraordinary as DHA never being replaced in 600 million years of eukaryotic evolution in the nervous system and in cell membranes. It is so extraordinary that there must be a missing role in biology that has yet to be discovered about why this is true. This blog is about that reason. THIS IS DECENTRALIZED MEDICINE.
18. So you might be wondering if DHA is so critical to humans how did it show up on Earth initially? Before DHA, Molybdenum was the key element for bacteria and archaea that used the sun for energy. The clocks in us measure and control the flow of entropy in us. The time stamping of light and dark on post-translational DNA by the mt DNA is how DECENTRALIZED MEDICINE WORKS. It is time you all wake up and stop supporting the criminals who created centralized healthcare.
19. THE LESSON IS OVER. REJECT CENTRALIZED IDEAS IN HEALTHCARE. Most of them are bad for you and good for the progeny of Rockefeller's plan.
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More from @DrJackKruse

Feb 11
This new blog is more explosive than the Epstein files, that I promise.

patreon.com/posts/150408576
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.Image
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?Image
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Read 9 tweets
Feb 10
Savages should know that glyphosate inhibits melanin production.  This means glyphosate causes on to lose control of metal chelation that controls mitochondrial pathway selection in humans.

Glyphosate acts as a noncompetitive inhibitor of the enzymes (like tyrosinase) responsible for synthesizing melanin. It disrupts the oxidation-reduction balance required to create the chelator of metals in mammals.

When the high-resolution, mammalian control system (driven by Melanin, L-amino acids like tyrosine, for precise NCC migration in the eye) is disrupted by modern stressors, like glyphosate, matrix deuterium loading  or the Cotton Effect of light, the mammalian system loses its physiological ability to control the metabolic "GPS" system of melanin which encodes the actions of our mitochondrial matrix using unpolarized sunlight via the RPE-SCN neural circuitry.

As a result,  In the absence of melanin to control those signals (Cu, Fe, Mn, Mo, and 2H+), the tissue defaults to a more primitive, "atavistic" genetic blueprint: the PaxB (Pax2/5/8) instruction set is employed.

Savages are also forewarned that centralized PhDs/MDs are Big Food and BigHarma technicians with bad attitudes and ignorant beliefs.
2. Let me show you a quantum leap between posts. You think you understand where I am headed with the post above?

LOL.

You do not.

Spoon feeding the public, in the long run, teaches us nothing but the shape of the spoon. The whole educational and professional training system is a very elaborate perception filter, which just weeds out people who are too independent, and who think for themselves, and who don't know how to be submissive for government programming. Education systems do not foster critical thinkers because they're dysfunctional to the institutions and the government. This is why I focus my teaching on how to think critically.

Try on this decentralized fact. It will make the centralized thinker head blow up, but it will intrigued the decentralized thinker to ask, what is Uncle Jack trying to tell me about Nature's recipe around light?

The Single Proton is the key Observer in figuring out what was buried in Genesis 1:1 to 1:15.

A single proton in Tryptophan is indeed a Time Crystal in reality. It is the "Observer" that allows the cell to know where the Earth is in its revolution. When we swap that proton for a deuteron, we aren't just changing an atom; we are changing the flow of Time in the organism.

Time is the most valuable asset we have. So you better understand how sunlight can put it back into you genotype.

CITE

optimalklubs.com/kruse-for-dumm…Image
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3. By framing health through E=mc^2 lens, I have identified the most fundamental "law" of biology: Mass and Energy are interchangeable, and Time is the denominator that determines which way the equation swings.  

Most of you missed that lesson in Vermont 2017.

Your RPE is the object in the eye that changes light to mass.

Time to bring you to speed with the MKULTRA blog on Patreon up next.

A lot of food gurs are going ot feel like they just got named in Epstein's files when I am done skull fucking their narratives.
Read 24 tweets
Feb 5
1. Should we give the 49ers players a free lesson on what the NFL and the team will never expose on their behalf?

We need to explain why the players are getting injured at an amazing pace since 2014 and that sotry begins with the evolution of the SCN in the eye that controls the circadian clock.

The eye clock is the key to the story of their injuries.
2. Today we know that vision and hearing evolved together dating back to the PaxB gene, which is a single gene controlling eye and precursors to hearing (mechanoreceptors) in box jellyfish.

This occurred before independent Pax 2 and Pax 6 genes showed up in primates much later. There are evolutionary connections between eyes and mechanoreceptors of the inner ear to the extent that during evolution are linked to melanin generation in those sense organs.

I told you earlier in the decentralized medicine series on Patreonmelanin was the favored semiconductor of all mammals post KT event.

This story of the 49ers players fits this my thesis well because the entire team is made of mammals who are post KT evovled.

If POMC/melanin is absent for any reason in these players, at any particular body place, for any reason, including nnEMF, it appears human neuroplastiticty allows sensory cells to shift their sensory modalities to an older phylogeny experienced in evolutionary history.

Why is this a big deal for the 49ers players?
3. The SCN is controlled by ipRCGs and is a well known blue light detecotr. The melanopsin phylogeny predates even primate evolution in time.

I think this happens in modern humans because of a loss of information and energy transformation in the embryo due to a lack of POMC or POMC translation in the parents cells and their germ lines that create their child = epigenetic defect planning = childhood diseases not of genetic causes which make up the bulk of childhood disease burdens today.

This means any 49ers players future children will also carry the burden of the 2014 power plant upgrade.
Read 38 tweets
Jan 31
Here is the irony: Attia advice was wrong.

**certain body secretions in people with diabetes often contain higher levels of carbohydrates (specifically glucose, the main simple carb involved) compared to people without diabetes.**. Look it up.

This is primarily due to elevated **blood glucose** levels (hyperglycemia) in diabetes, which can cause glucose to spill over or leak into various secretions when blood levels exceed normal thresholds. Recall Attia never finished his residency. He charges 200K to see him. I’m sure many of his patients would expect him to know the basic of human secretions is based on blood sugar levels

Here's a breakdown by common secretions that have more carbs

-vaginal secretions are high in carbohydrates in diabetic women.

- **Urine** — In uncontrolled or poorly managed diabetes, urine frequently contains significantly more glucose (a condition called **glycosuria** or glucosuria). Normally, healthy kidneys reabsorb nearly all filtered glucose back into the blood, so urine has little to no detectable glucose. When blood glucose exceeds the renal threshold (typically around 160–180 mg/dL), excess glucose appears in the urine. This is a classic sign of diabetes and can be much higher than in non-diabetics (who usually have negligible amounts).

- **Saliva** — Multiple studies show that salivary glucose levels are higher in people with diabetes (both controlled and uncontrolled) compared to non-diabetics. For example, mean salivary glucose is often around 13–14 mg/dL in diabetics versus 4–5 mg/dL in healthy controls. This occurs because high blood glucose increases leakage or diffusion of glucose into salivary secretions.

- **Sweat** — Sweat glucose concentrations are generally low in everyone (often 1–2% of blood levels), but research shows a strong correlation between sweat and blood glucose. In diabetics with higher blood glucose, sweat glucose is correspondingly elevated (e.g., potentially 0.3 mmol/L or more when blood is very high, versus lower in non-diabetics). This is why sweat is being explored for non-invasive glucose monitoring devices.

- **Tears** — Some evidence suggests tear glucose can also be higher in diabetics and correlates with blood levels, though this is less commonly studied than the others.

In summary, while not all secretions are equally affected and concentrations remain much lower than in blood, **diabetics typically have more glucose (a carbohydrate) in urine, saliva, sweat, and possibly tears** when blood sugar is poorly controlled. This doesn't apply universally to every diabetic at all times (e.g., well-controlled cases may show minimal differences), but it's a well-documented pattern, especially in hyperglycemia. If this relates to a specific health concern, consulting a doctor for personalized testing is recommended.
2. This goes to show you just how uninformed Attia is on the basics. High blood sugar (hyperglycemia) can occur due to various conditions and factors outside of diabetes, potentially leading to similar effects on carbohydrate (primarily glucose) levels in body secretions like vaginal secretions, urine, saliva, sweat, and tears. Physical or emotional stress: Acute stress from illness, infection, injury, trauma, surgery, tech screen abuse, cell phone use triggers the release of hormones like cortisol and epinephrine, which raise blood sugar to provide energy for the "fight or flight" response. High-intensity workouts can cause a short-term spike in blood sugar as the body releases stored glucose for fuel, especially in non-diabetics unaccustomed to such activity. Poor sleep quality from blue light and Earpod use disrupts hormonal balance, leading to insulin resistance and elevated glucose levels. Attia is known to believe that doing 100 push ups limits nnEMF risk. Look it up. He told this to Chris Williamson on a live IG post.
3. What else did Attia miss in his answer to Epstein? Cushing's syndrome: Excess cortisol production (often from adrenal tumors or prolonged steroid use) impairs insulin function and raises blood sugar.

Polycystic ovary syndrome (PCOS): This common hormonal disorder in women causes insulin resistance, leading to chronic hyperglycemia.

Acromegaly: Overproduction of growth hormone from a pituitary tumor reduces insulin sensitivity and elevates glucose.

Other hormonal issues: Conditions like hyperthyroidism or pheochromocytoma (a tumor causing excess catecholamines) can also contribute.
Read 5 tweets
Jan 31
In my decentralized framework, this is exactly how the system is wired. The nipple-areola complex acts as a quantum-optical sensor, and the infant’s saliva is the fiber-optic cable delivering a real-time UPE (ultra-weak photon emission) status report from the child's mitochondria to the mother’s "manufacturing plant."

This isn't just convenience; it is a biophysical "handshake" that ensures the survival of the post Cambrian hardware mammals need to thrive.

1. Saliva as the "Optical Bio-Feed"

Saliva is a highly structured, mineral-rich fluid. In my thesis, it serves as the medium for optical information transfer:
The Child’s Signal: When a calf or child is sick, their internal "optical smog" increases. The VUV (Vacuum Ultraviolet) and chaotic UPEs produced by their congested Complex II are transmitted through the saliva. Congestion usually is due to reverse electron flow or deuterium.
The Mother’s Sensor: The areola is one of the most melanized and innervated tissues in the mammalian body. Melanin here doesn't just protect against the sun; it acts as a broadband transducer like an optical scanner in the grocery store. It "reads" the frequency of the biophotons in the saliva.

2. The Backflow "Optical Loop"

Research into the "infant-led" backflow confirms that when a child suckles, a vacuum is created that pulls saliva back into the mother's mammary ducts.
Information Sensing: The mother’s immune-sensing cells in the ductal walls "listen" to the ROS/RNS signatures and UPE entropy in that saliva.
The Response: If the child’s saliva "shouts" of deuterium congestion at cytochrome two because succinate is elevated  or viral "optical noise," the mother’s brain (via the SCN-hypothalamic oxytocin posterior pituitary pathway) triggers a change in milk composition. She begins to "distill" more NPD1, Iodine, and IgA antibodies into the milk to act as a "quantum reset" for the child’s mitochondria.

3. The "Rotating Mom" Phenomenon (Allomaternal Nursing)
Why do calves or elk rotate moms? In my framework, this is "Frequency Matching":
Metabolic Matching: A calf may instinctively seek a different "frequency" of milk if its own mother’s melanin-metal hardware is jammed (perhaps she spent too much time in a "dirty" environment like inside a barn under fake light).
Information Diversity: By "sampling" different mothers, the young mammal is essentially "crowd sourcing" optical coherence. They are looking for the milk with the lowest deuterium/highest DHA-D3-Iodine ratio to stabilize their own emerging Faraday cage.
Modern humans with nnEMF toxicity who cannot breast feed their children due to a lack of production should be considering what elk do when they are faced with the same problem.  This concept is foreign to humans because they do not observe nature carefully enough.

4. Milk as a "Re-Cambrian-ization" Serum

Mother's milk is the ultimate low-deuterium, high-DHA, solar-coded fuel.
Deuterium Depletion: Milk fat (cream) is naturally low in deuterium, helping the child build a "clean" 14 Angstrom tunneling gap in their developing mitochondria.
Melanocortin Programming: The act of nursing at sunrise/sunset ensures the child’s Leptin-Melanocortin pathway is synced to the mother’s, preventing the "Proterozoic regression" that leads to neolithic disease later in life.
The ranch memories you have are of a Quantum Ecosystem in action. The child’s saliva "tells" the mother's nipple exactly how the child's internal "mercury lamp" (deuterium) is burning. The mother then alters the "Optical Duty Cycle" of her milk to quench the fire.
Does this explain why formula-fed infants (drinking high-deuterium, seed-oil-heavy milk) are essentially being "pushed into the Proterozoic mud" from birth, as they lack this bidirectional optical feedback loop?  Yes, it does but few seem to care about it.

This lesson also has deep information for the diseased breast too. Men can help their women with diseased breasts by kissing their nipples religiously to transfer information to their women about how they feel for them.  This will be highly stimulatory and healing.

Cells and Stars have a lot on common.  When they fail they have mechanisms that feedback on themselves that lead to the possibility of future survival if conditions are met.  In a star when it burns through its fuel source its core gets to iron and the star begins to emit microwaves.  The microwave radiation interacts with the D shell electrons of Fe and it blows up in a super nova so the atoms it creates in this destruction can be recycled to something with more life in the cosmos.  Cells in our body use a similar idea in apoptosis, autophagy, and ferroptosis.

In my decentralized framework, the brain and breast in cancer do not operate in the same fashion regarding IDH protection because their "optical hardware" and evolutionary duty cycles are fundamentally different. Neurons are not epithelium, but breast tissue is.
While the brain relies on IDH mutations from its DHA-rich antenna to create UPEs to work and eventually help create some VUV smog from complex two back up to clean the dirty chemistry in cancer, the breast mitigates oncogenic risk through a different mechanism:

It uses the DHA-Iodine-Melanin triad.

1. The IDH Paradox: Why the Brain Needs It, But the Breast Doesn't

The brain is the ultimate "quantum sensor" that can feedback on itself and it must maintain 24/7 DHA coherence.  DHA allows for this.
The Brain (DHA Antenna): When Complex II jams, the resulting VUV emission from Deuterium threatens to shatter the DHA antenna. The IDH mutation occurs as an emergency "filter" to deplete deuterium and lower the VUV entropy.  DHA, as a PUFA explodes like the star and in its destructions NPD1 and Elovanoids along with UPEs are made which are highly anti-inflammatory.  The released UPEs feed back on IDH and mutate it in such a specific way that the brain is able to make more deuterium depleted water because of this interaction than it could before to help self sustain its survival.  This is how most low grade gliomas begin.  This process does not happen in GBM transformation due to a lack of DHA in the brain.
The Breast (The Glandular Sink): Breast tissue is not a primary "spectrometer" like the brain. Instead of a mutation-driven shunt (IDH), the breast uses Iodine as its primary "quantum ground." In the breast, the "De-Cambrian-ization" of its mitochondria is mitigated by the concentration of iodine in the Ductal-Lobular Units.
2. How the Breast Mitigates Risk: The Iodine Shield
If the brain uses the IDH mutation to "buffer" the VUV smog itsdeuterium squeeze, but the human breast uses Iodine to "quench" the fire in the cytochrome 2 Fe-S clusters that begin the disease from reverse electron flow from cytochrome 2 dysfunction.The Delta-Iodolactone Mechanism: Iodine is required to form iodo-lipids (delta-iodolactone). These act similarly to Bazan’s Elovanoids in the brain, but they are specifically tuned to inhibit the Warburg Effect in glandular tissue.
Melanin & The Nipple: The high concentration of melanin in the areola/nipple is not a "decoration." It is the Optical Port that harvests solar UV/IR to control the metal flux (Cu, Fe) in the underlying breast tissue to make sure the TCA and urea cycle are the primary pathways used to avoid cytochrome 2 congestion and Fenton reactions of Fe-S couples.
The Sink: The breast is designed as a "DHA sink" (for lactation). It mitigates VUV damage by using Melanin and Iodine to sequester the "dirty" Iron noise created from a lack of sun, nnEMF, or polarized light.  nnEMF for the breast is the stimulus that leads to ferrotoptosis destruction of the Fe-S couples and this mimics the process that happens in a star.   When Iodine is missing, the breast cannot "ground" its own self created UPE field, leading to DCIS or invasive carcinoma without the IDH "slow-burn" protection seen in the brain.
3. The Unified "De-Cambrian" Failure
Both cancers represent a Proterozoic Regression, but the "breakdown" follows the tissue's specific metal hierarchy:Brain Cancer (GBM/LGG): A failure of the DHA-VDR-IDH loop. The brain tries to mutate (IDH) to survive the VUV fire.
Breast Cancer: A failure of the Melanin-Iodine-DHA loop. Without Iodine to "buffer" the Iron D-shell electrons, the breast tissue undergoes a rapid phenotypic regression and this is how cancer begins.Image
2. Integration with Melanin and the Sun

The synthesis of both molecules is tied to the Melanin-Metal hardware:
The Sun: UVB/IR input on the skin stimulates the Leptin-Melanocortin pathway. This manages the Copper (Cu) and Manganese (Mn) levels required to build the antioxidant "Mn-SOD shield."

The Translation: Coherent UPE signals (from healthy mitochondria) then tell the cell to cleave the lipids needed for NPD1 or gamma iodolactone
.
The Result: You have a "protected" post Cambrian cell that can use oxygen via the TCA/urea cycle without producing the ionizing VUV UPEs that destroys the genome.

Bazan’s Docosanoids (Brain/Retina): These cleave from DHA to form a "Faraday cage" of 22 carbons. Their purpose is to quench the VUV (Vacuum Ultraviolet) smog emitted by deuterium in the high-density neural environment.Image
3. UPE isn't mere waste; from quantum biology, these photons (or associated fields) may mediate non-local signaling, akin to coherence in radical pairs or bystander effects.

Intensity/spectrum reflect metabolic flux:

Aerobic paths (TCA) produce more ROS/UPE than anaerobic (glycolysis); stress shifts spectra (e.g., UV-linked UPE from glycolysis/peptides). Melanin optimizes by calibrating inputs—solar photons tune metal-ROS-UPE, enabling adaptive switches via redox/epigenetic relays (e.g., NAD+/SIRT1, from the Decentralized Medicine series of blogs on Patreon).

patreon.com/DrJackKruse
Read 7 tweets
Jan 29
Plan B in El Salvador is all about the Tether gold play. This is how they want to rescue things for the surveillance state. Image
2. What is the rescue plan? Remember the famous now deleted Bessent tweet about DJT/Treasury plan to confiscate Bitcoin for the US Bitcoin Reserve? That was updated once the backlash on the tweet went out. Now it is about using Tether to centralize gold as they implode the Dollar and they will confiscate the Gold.

I've argued for 10 years that Bitcoin is a superior form of "trust-minimized" money compared to gold due to the high costs of verifying gold's authenticity.

This is the ability to own and verify an asset without relying on a third party (like a Central bank or Treasury of a government). Historically, gold's "trustless" nature was its greatest strength, but Savages now know this strength has been lost because most gold now sits in centralized vaults. This is why DJT won't let anyone audit Fort Knox. Why audit what you plan to steal?

The Cost of Validation for gold is steep so no one in the USA will want to pay that freight so now we are on the honor system for the Treasury.

Anyone who has owned gold knows that verifying that a gold bar before a sale/audit is real and pure requires specialized equipment, chemical tests, or expensive third-party audits. Because this is so difficult to do, you must have an inherit "trust" the vault or institution holding it for them. + Treasury and Bessent play. What did they do in 2025. They brought their middle man in. Tether. Go check if I am bullshitting you. Tether has bought more gold in the last 18 months than they have bought Bitcoin. Why? They are storing what the thieves in the industrial miliatry surveillence state will take down the road when the retards are sidetracked by circus maximus of some other psy-ops.

Why isn't Tether buying Bitcoin in this case? Anyone with a simple computer or smartphone can instantly verify the entire history and authenticity of their Bitcoin by running a node or using a block explorer. This "validation" is nearly free, making it more decentralized and harder to seize. Tether should be buying T bills but instead is buying Gold Reserves for the Zionist bankers to steal soon. Got it, my Savages.

Bitcoiners should know and remember their history better. This gameplan was used to before in 1933 during the Great Deperession to make it easy for governments to confiscate it.....Remember FDR's EO?

The U.S. did this already with Executive Order 6102 in 1933.

Looting and Centralization are the play. For thousands of years, physical gold was frequently stolen or seized by empires. To protect it, it was eventually moved into highly secure, centralized vaults (like those at the Federal Reserve Bank of New York or the Bank of England under control of the Treasury Head.

If the steal the gold this will tank markets including Bitcoin and then the Treasury will come in an sell gold at astronomical prices to buy Bitcoin at crashed Prices. This is how the Rockefeller and Rothschild Banks plan to do this.

If you know your history this is how the same guys did the scam during the Napoleaonic Wars. They manipulated the market with a psy-ops. In 1812 it was the Battle of Waterloo.

WAKE THE FUCK UP.

If you knew this history would would not be so gullible.Image
Read 5 tweets

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