Remember the battle for the Nobel Prize between the discovery of HIV from Montagnier versus Robert Gallo in 1983?
Do you know that Robert Gallo began studying HIV in the jungles of the Congo in chimpanzees during the oral polio virus trials.
The first oral polio vaccine was aerosolized oral spray that caused cancers all over the mouth and sinus system. A bioweapons company did the work for DoD and Robert Gallo was on that team. Things you just do not know when you do not know your history. Did you know that Fauci support the Nobel Prize for his friend Gallo over Luke Montagnier?
Coincidence or might it be related to why Reagan hired Fauci in 1982?
3. The first bioweapons lab on Magazine Street in NOLA and the work done at the US Public health hospital and Henry Clay Street in NOLA was transferred to the Tulane Primate Center in Covington Louisiana under the direction of Dr. Riopelle. When it became clear after the JFK killing in the mid 1960s that these simian viruses were behind many new human diseases like cancer and eventually HIV they were transferred to Fort Detrich as I laid out in my pod with RFK Jr. In the beginning Fort Detrich was an dual purpose base with the ARMY and CIA sharing thefacility and the bioweapons labs added to the mix as the science of Dr. Mary Stewart and Mary Sherman was developed by the CIA and industrial military complex.
4. The bioweapons lab in NOLA gave the military important bioweapon clues. Namely that nnEMF drive pathogenicity and it could be concentrated if many different viruses from competeing species were mixed before irridation. They were very deadly. These things were developed at Fort Detrich from 1963-68 in experiments called the Special virus leukemia Program.
5. This shows you where the military was in 1968. They were at a macro level dealing with data points in dead animals looking to see what was most effective in killing them. The miliatry was not the molecular level that one would need at furin cleavage sites to know the proper AMO physics to carry our mass death in living things. That science developed after Reagan hired Fauci in 1982.
When one plots the data of chronic diseases to when Fauci entered the industrial military health complex the data points do not lie. They tell a story that shows you it it not a story about food. It is a story of AMO physics and light to ruin mtDNA biology.
6. The most interesting finding from this Fort Detrich program was that the industrial military program was not looking to cure cancer, it was looking to make it more lethal. They found using animals closest to the human genome were the most deadly to humans. And then they amplified the effect through the early Nixon administration. @Kevin_McKernan The pathway to policy was clear. A new bioweapon policy was developed around vaccines using gene products needed to be developed by the military. This is where the ideas were born.
7. This paper really shows the origin of HIV. When the industrial military complex decided to mix the serum or primates and human serum togther and monitor the effects some very interesting findings started to show up in the literature early in Nixon's administration. This was 2 years before Nixon and Alton Ochsner launched the "War on Cancer" policy. That policy was designed to create a pile of money for covert bioweapon development. This money was laundered from the NCI to the military to continue on the pathway that General Groves began with Ochsner in NOLA during the Cutter Incident.
8. In 1970 they moved into the molecular medicine to see where the cancers can be recombined with across species. These are the genesis of gain of function studies done on US soil. This was legal before the 2001 Patriot Act. Now it is illegal and carries the penalty of death by Treason.
9. The last tweet shows you how viral chimera's were first built. You need to know that scientific accountability under our Constitution has not changed much since WW2. It rests with the Executive branch and this is why Gen. Groves capture this branch first in his silent coup on America by his shadow government. Why is this slide important. You'll notice the myriad of boxes who have to perform oversight for science and scientific misdeeds.
Groves had a lot to do with setting this system up because it gave the government scientific denialble plausibility in cases of misdeeds. I explained this to @nayibbukele when we met about the Constittional Amendment for his country. I told him RFK Jrs plan would not stop the problem with a Benjamin Rush like Amendment added to the ddcument because the industrial military complex knew this was the DOCUMENT's main weakness and they could exploit it using chronic disease management.
10. The next slide should give you chills. In 1969 they told Congress exactly what they were up to in viral chimera building and why they were doing it. Congress had ZERO issues with it and they allowed this via the oversight process. This was FUNDAMENTALLY why I disagreed with Bobby during the Tetragrammaton podcast with Rick on how to handle the chronic disease epidemic at its source.
We need a Constitutional Amendment to stop this freight train of the Deep State actors. This is when the military began to ensnare and capture the legistaltive branch of government. @KONCRETE
11. The industrial miliatry complex knew exactly what they were doing and Congress and Nixon helped them. If you listened to what I said about Nixon and what Bobby said about Nixon you'll notice we differed on our opinions of his legacy. This Act to Congress explicitly said that the military was now capable of making a bioweapon that would be immune to human immunity.
12. For the non believers that your own government did this, this is the entire logic chart they used in the annual report of the project from 1972 when the War on Cancer was used as a psy-ops on America.
13. Fort Detrich was where mammalian viral pathogens were mixed in lab test tubes accross multiple species like cards in a casino deck to try to find the nastiest disease the miliatry could use to kill effectively. The slide below shows you the basic of how the system was developed by your own government.
14. So when someone asks you where disease really begin........and you answer food. You're an idiot because you have no idea about the history of how this process began with the Manhattan Project in the 1930s.
15. Once they created a virus that could collapse the enture immune system, they decided to find out how to alter immunity so that diseases could come on faster. Here was a paper I was assigned to read as a neurosurgery resident to understand the biology of the fast growing cancer called GBM in humans. Most autoimmune conditions are related to these mechanisms. Many cancers are. Many other chronic disease epidemic diseases are also linked to neuroimmune defects.
16. Why was Peter Duesberg an HIV denier. If you read the literature as I did, you'd know why. He knew where it came from. This is the same story we just saw with COVID that happened 40 years ago in HIV.
17. Deusberg knew what many of us knew that simian virus was grafted onto the human system and the vector was the VISNA platform. The result was the HIV "1983 discovery" It was no discovery at all. Any financial forensic journalist could perform a details accounting to find out where the money came from and went to, to figure out this "medical enigma"
18. This is the patent to making the monster Hepatitis B vaccine that all physicians had to take. Note the highlighted area. You now see 20 yrs after the list of simian viruses the military was using they were now producing vaccines with the science as a delivery mechanism. Now you can see why there was a need for Fauci 7 years later and the vaccine law in 1986 when the techniques moved from the DoD to BigHarma partners.
19. That Hepatitis patent was used by Merck in their Heptavax trial in 1978. That trial was the basis of why every healthcare professional and soldier had to take this jab. So I know my history and I know what the government is capable of. It is time some of you get your heads out of your ass and know it as well.
20. What was in the COVID jabs? Simian virus 40 promotor.
21. @threadreaderapp make me a roll
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Wondering if you'd be able to break down what happened after I took Venlafaxine (Effexor) a few years ago and if there's any specific things needed to be done to hopefully repair any damage.
After what I believe was a spontaneous CSF leak that happened one night and started all my chronic issues I was diagnosed with vestibular migraine around 3 months later.
Venlafaxine 75mg was indicated for this so I was on it for around 12 months (give or take the 3 months wean I did).
Within 3 weeks my emotions went numb, I lost my libido, erections and ability to pretty much feel love or any strong emotion. There was a very definite and obvious "change" but I believe I still had the ability to focus and enjoy hobbies etc.
After deciding to taper off, I would get brain zaps and all the other jazz that comes with it. After fully tapering, I was then introduced to anhedonia. Unable to feel or enjoy anything, unable to focus on anything for too long without getting the irritable and feeling like I need to do something else etc. Essentially feel there's been a permanent change since starting this.
This has improved slightly but not even close to where I'd like to be. Add all the daily brain fog, memory lapses etc and my brain is running on empty.
Does this need anything specific additional to the core light, water & magnetism?
Listening to this months webinar (October 2025) you mentioned accutane extending recovery from 6 months up to 5 years. This prompted me to ask this question and about my accutane use in the future as this is a huge jump in recovery time and shows how powerful these drugs are.
3. Reasons Why Venlafaxine Could Cause Issues, Based on My Thesis
My thesis posits that life's core "code" resides in conserved correlations of phase, spin, and topology, geometric invariants that maintain coherence beyond mere voltage gradients. Man-made electromagnetic (EM) pollution disrupts this coherence, leading to health risks like aging, cancer, and failed regeneration. Voltage is merely a "courier," while true memory and form emerge from photonic organization of spin and topological symmetry.
Venlafaxine, as a synthetic molecule introduced into this already polluted EM environment, would act to exacerbate disruptions by interfering with biological EM phenomena. Below, I list hypothesized reasons grounded in its structure, spectra, pharmacology, and potential EM interactions.
These are hypothestical extensions based on my published framework, drawing from known drug effects and bio-EM principles (e.g., biophotons, ion flows, and field coherence), while acknowledging that direct studies on venlafaxine-EM-biology intersections are limited because BigHarma isn't going to dump on its own product with truthful decentralized science.
1. The terms anaplerosis and cataplerosis describe reciprocal and correlative reactions involved in the function of the TCA/urea cycle. The enzymatic steps in these processes have long been known, but the overall concept of a linkage between anaplerosis and cataplerosis should be underscored because the balance between these two processes controls the entry and exit of TCA cycle anions.
Anaplerotic and cataplerotic reactions are involved in the ultimate disposal of all metabolic intermediates. The metabolic role of anaplerosis and cataplerosis in amino acid metabolism varies with the light environment, specific organs and is dependent on the nutritional/metabolic status of the individual.
If the AM sunrise is seen by the eye, skin, and sensed by the gut via the skin clocks, during feeding, the intestine is an important site of catabolism of enterally derived amino acids, whereas in the starved state amino acid catabolism occurs primarily in the kidney, liver, and muscle. The light environment is critical in how anaplerosis and cataplerosis operate in people.
Every tissue differs in how it uses anaplerosis and cataplerosis.This implies the regulation of anaplerosis and cataplerosis is very dependant on deuterium kinetics in the matrix from normal or abnormal metabolic and physiologic states.
Methionine: Propionyl-CoA forms as a catabolite of methionine, threonine, and the branched-chain amino acids. β-Oxidation of fatty acids with an odd number of carbon atoms yields propionyl-CoA. The oxidation of the side chain of cholesterol also yields propionyl-CoA. Thus, propionyl-CoA is derived from the catabolism of lipids and proteins.Propionyl-CoA is converted to succinyl-CoA, which is oxidized or converted to glucose by way of oxaloacetate and pyruvate. Succinyl-CoA may also form δ-aminolevulinate, a precursor of porphyrin biosynthesis.
This is critical in oncogenesis because cancer cells need brisk ECT which means that cancer cells can use methionine to usurp oxygen using methionine to increases both angiogenesis and hemoglobin production to make sure that oxygen delivery is brisk and apoptosis stays inhibited PROVIDED VDR/D3 and/or UVA are absent to slow ECT flow.
NO is used to slow ATPase as a braking mechanism when oxygen is a toxin. This is a remnant from our GOE evolution before heme proteins and melanin were innovated to protect us as a firewall from oxygen. NO is liberated by UVA light and NIR.
Update your biochemical models because they are all broken.
2. Anaplerosis and Cataplerosis: They are Light-Dependent Gatekeepers of TCA/Urea Cycle Dynamics and Metabolic Fate
From first principles, metabolism is fundamentally an energy and information flow process, governed by thermodynamic gradients where sunlight provides the primary low-entropy input to drive organization and efficiency.
The tricarboxylic acid (TCA) cycle, also known as the Krebs or citric acid cycle, serves as life's central hub for oxidizing nutrients to generate ATP, but it doesn't operate in isolation.
Anaplerosis (replenishment of TCA intermediates like oxaloacetate or succinyl-CoA) and cataplerosis (removal of these intermediates for biosynthesis or disposal) act as reciprocal OPTICAL valves, ensuring the cycle's continuity while adapting to cellular demands
3. Ultimately, these processes dictate the disposal of all metabolic intermediates, linking carbon, nitrogen, and sulfur flows across pathways like amino acid catabolism, fatty acid oxidation, and urea cycle.This balance controls the entry and exit of TCA anions (e.g., citrate, malate), preventing depletion during high biosynthetic pulls (e.g., gluconeogenesis, lipid synthesis) or overflow during nutrient excess.
Ultimately, these processes dictate the disposal of all metabolic intermediates, linking carbon, nitrogen, and sulfur flows across pathways like amino acid catabolism, fatty acid oxidation, and urea cycle.
There is only one kind of shock worse than the totally unexpected outcome: the expected for which one has refused to prepare. This is the new jouney for those who complied with tyranny and joined the experimental group the last 5 years.
The expected always happens and this can be a problem too. Sometimes the most scenic roads in life are the detours you didn't mean to take. This is true for the control group.
The results of traveling the road less traveled surprises us. So, would you really like to know your future?
If your answer is yes, think again. Not knowing is the greatest life motivator for thriving for those of us who rejected compliance.
So enjoy, endure, survive each moment as it comes to you in its proper sequence -- a surprise. Embrace the chaos and the suck for a change, but never comply with tyranny.
2. People who complain they have no time or wish they could control how they spend their time to do what they should are stuck in a low dopamine state because of the light they live under. Few of them are aware of the implications.
Here is how it works: Know how to get the most results in the least amount of time. That’s the ultimate aim of productivity skills. Savages know we all have the same amount of time in a day so when somebody tells you they do not have time to do something they have a made choice with their time to do something else. In the age of information, ignorance of the wisdom of reality and nature is a choice.
3. With that said how come equatorial Africans never seem to get cancers on the equator when they make the daily choice to be in the strongest sun on the planet possible, but people who have no time because they are working under fake light and nnEMF seem to get all denovo or jab induced cancers, and especially the worse types?
He said, "the same command becomes a metabolic loan the body can’t repay."
This is why evolution put the VDR recpetor on the IMM. When you have UV and IRA/NIR you can repay the loan. This means the SUN is TINA. Why? It slows the charge on the IMM.
It should not make sense why I do use affliate codes for red lights.
They are a half truth to those with electrical resistance problems in the IMM.
You always need purple and red to pay the loan back. Purple and red together renovate the poor engines to restore the default state.
2. The U.S. has the highest first-day infant mortality out of industrialized world About 11,300 newborns die within 24 hours of their birth in the U.S. each year, 50 percent more first-day deaths than all other industrialized countries combined.
This is that awkward moment when the statistics confirm that the experts are wrong about something, and the children are dying because of it.
The problem in the U.S. is that many of the babies born here are premature.
What are the reasons that babies are born prematurely?
Risk Factors for Premature Birth are all correlated with artificial light melanopsin damage. Can you imagine that?
Many risk factors can be reduced or eliminated altogether. Talk to your doctor or midwife about your individual risk factors and what you can do to diminish them.
Risk factors include:
Prior premature birth.
jaundice requiring blue light therapy
Multiple pregnancies.
Uterine or cervical problems.
Chronic high blood pressure.
Diabetes.
Smoking.
Jab compliance.
Age.
Lack of UV exposure prenatally.
Poor nutrition due to missing DHA.
Untreated infection.
3. What do bears and humans have in common? Both are carnivore mammals who have adapted to high latitude living over their evolutionary history.
Bear testosterone levels peak in the Spring and early Summer in high latitudes when UV light and IRA/NIR light return in unison to their environments.
Why does their hormone panel change?
Terrestrial solar light determines mating and fertility in mammals at all laltitudes but it most obviously seen at high latitudes where UV is not stable yearly.
What happens when humans bombard themselves with fake light they make?
You get an infertility epidemic in humans! = FACTOR Y on display.
This makes the OB/GYN's happy and rich. It also creates a lot of misgendering, beta, and mental illness. It also creates a lot of suboptimal children with developmental issues. We should never force nature into doing something she says should not occur.......unless we are ready for the collateral damages. academic.oup.com/biolreprod/art…
1. How will the transhumanist technologists use AI in the future?
I often think of how compliant we have become. Anytime you use Google or have an iPhone or any phone for that matter, you have to ‘agree to the terms’, every Apple update there is something new to comply with. This is a problem of how they suck you into the matrix. Your land line phones never did this.
The transhumanist tech companies know the addicted will comply and agree to any terms to suit their addiction to technology and don’t bother to read anything they want you to bend the knee for. The trade off for entertainment for the soul has been around for a long time. But the manner in which these transhumanist are capturing people should be unsettling to anyone who can think.
2. Wireless radiation is being used to surveil people without their knowledge or consent, even if they aren’t wearing a “smart” device or holding a cellphone, according to the authors of a new study.
The study authors engineering faculty members with the Institute for Systems and Computer Engineering, Technology and Science at the University of Porto, Portugal posted their report Jan. 24, 2025 on the Cornell University open-access research website, arXiv.
The study showcases hardware the authors designed that leveraged ambient wireless radiofrequency (RF) radiation to detect and render a visual image of human activity such as waving a hand or a person’s breathing rate with over 90% accuracy.
Their design involved a thin programmable surface a Reconfigurable Intelligent Surface (RIS) that communicates with computers and artificial intelligence (AI).
3. RIS can manipulate and steer Wi-Fi signals in controlled ways, explained Fariha Husain, manager of Children’s Health Defense’s (CHD) Electromagnetic Radiation (EMR) & Wireless Program. “By adjusting how radio waves reflect off this surface, the researchers were able to enhance signal-sensitivity and improve their ability to detect subtle human movements.”
Husain said:
“RIS panels can be strategically placed to optimize wireless signal reflection and steering and may take any shape or be integrated into objects. Indoors, they can be mounted on walls, ceilings or furniture.
“Outdoors and in urban areas, they can be installed on offices, airports, shopping centers, lampposts and advertising billboards. Additionally, RIS panels will enable smart city surveillance by tracking pedestrian and vehicle movement.”
RIS hasn’t been incorporated into current wireless networks but it’s in the works for 6G, according to W. Scott McCollough, chief litigator for CHD’s EMR & Wireless cases.
“Future 6G networks will have RIS functionality built in,” he said, “and it would not surprise me if they don’t implement RIS in the future 5G updates.”
What do you know about the Stiles-Crawford effect in a healthy eye? What if I told you this effect is how we sharpen central vision and narrow the periphery of the retina from too much blue light. Would you believe it? Did you know melanopsin has a specific topographic map on a healthy retina? A lesson no has taught you is incoming.
2. All opsins are topologic insulators. You might want to read that threadroll above now to understand topology well.
Topology changes in a cell = geometry change of cristae = UPE change from mitochondria = the optical signal changes in the same tissue altering physiology.
So what happens if you sustain mitochondrial damage in your retina's colony of mitochondria to the Stiles Crawford effect?
What are the implications?
3. The Stiles–Crawford effect (SCE) is the human eye's phenomenon of reduced light sensitivity when light enters the pupil from its periphery compared to the pupil's center. This effect is due to the optical properties of photoreceptors, which act as waveguides and are aligned to channel light towards the fovea, the central point of vision. The SCE makes vision less sensitive to light entering the periphery, thus reducing glare and improving visual clarity. It also keeps a lid on the amount of blue light the periphery the retina gets.
This sharpens vision, makes myopia, glaucoma, cataracts, hyperopia, and AMD almost impossible to get. Makes one resistant to mental illness too. Makes one impervious to diabetic transformations. Makes neurodegeneration rare.