• Description

    LEANBLISS REVIEW (( NEW BEWARE! )) LEANBLISS WEIGHT LOSS - LEAN BLISS REVIEWS - LEANBLISS SUPPLEMENT

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    What Is LeanBliss?
    LeanBliss is a revolutionary weight loss supplement that targets unwanted weight by optimizing blood sugar levels. Formulated with natural ingredients, LeanBliss boasts effectiveness, efficiency, and, most importantly, safety in managing blood sugar levels while offering various associated health benefits.

    Official BUY LINK https://leanbliss24.com/text.php#aff=Vivek5555

    Packaged in chewable tablet form, each bottle of this weight loss and blood sugar-controlling supplement contains 30 tablets, ensuring the inclusion of vital ingredients necessary for its intended effects. With a focus on quality, LeanBliss is free from GMOs or stimulants that artificially induce health benefits. Additionally, its gluten-free and dairy-free composition underscores its safety for consumption.

    LeanBliss Ingredients: What Goes Into Its Making?
    The ingredients in the formulation of LeanBliss weight management aid have been informed to be natural by its manufacturer. When specifically looking into these, it has been noted that there exists a potential blend of exotic herbs, which are expected to provide the intended results when taken. These include the following:

    Ceylon Cinnamon Bark: It is needless to mention this type of cinnamon bark is native to Sri Lanka. Multiple health benefits are associated with this plant, one of which is reducing inflammatory response in the body. Since a majority of the inflammatory reactions are due to chronic health conditions, such as diabetes, arthritis, and heart disease, the cinnamaldehyde, an active component contained in the Ceylon cinnamon bark is what renders this plant its anti-inflammatory properties. The plant also helps enhance metabolism, which is essential in reducing weight.

    Corosolic Acid: A vital component present within the Banaba leaves from the tree of Banaba (scientific name: Lagerstroemia speciosa) found in Southeast Asia, Corosolic acid helps treat diabetes because of the antidiabetic properties contained within it. Meanwhile, it would be worth noting that every part of this plant is noted with some or other health benefits. For instance, its fruits and roots have been found to have analgesic properties.

    Citrus Sinensis: This ingredient in the LeanBliss formula is considered to be useful in weight loss for overweight people. It is alternatively termed as Sicilian blood orange, which is beneficial in tackling stubborn weight gain in people who are otherwise medically healthy. Notably, it is the anthocyanins and cyanidin 3-glucoside present in this orange that make it effective in reducing unwanted weight.

    Saffron Bulb Extract: Saffron which is often used as a spice is also bestowed with medicinal properties. The anticancer property of saffron helps prevent and treat cancer. The saffron bulb extract is also helpful in treating PMS symptoms in women, such as headaches, pain, irritability, and cravings.

    How Does The LeanBliss Formula Work?
    The LeanBliss weight loss support supplement operates by regulating blood sugar levels, thereby facilitating healthy weight loss. Given the prevalent issues of obesity and overweight in the United States, medical interventions for these conditions often come at considerable expense. Despite numerous attempts, such as restrictive diets, intense workouts, and starvation, many individuals struggle to shed unwanted weight.
    Official BUY LINK https://leanbliss24.com/text.php#aff=Vivek5555

    In response to these challenges, US physicians have sought to develop supplements that are natural, diet-friendly, and yield optimal results. LeanBliss, a fat-burning formula, emerges as a product of such efforts, purportedly created by a doctor and supported by robust clinical research and findings. Contrary to conventional beliefs, studies suggest that fluctuating blood sugar levels may precede weight gain, rather than vice versa.

    This revelation underscores the significance of pancreatic function, particularly insulin production and glucose utilization, in regulating hunger cravings and weight gain. Understanding this mechanism sheds light on how the LeanBliss dietary formula operates, offering insight into its design and functionality.

    Official BUY LINK https://leanbliss24.com/text.php#aff=Vivek5555

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    Description LEANBLISS REVIEW (( NEW BEWARE! )) LEANBLISS WEIGHT LOSS - LEAN BLISS REVIEWS - LEANBLISS SUPPLEMENT Official BUY LINKπŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡ https://leanbliss24.com/text.php#aff=Vivek5555 βœ…What Is LeanBliss? LeanBliss is a revolutionary weight loss supplement that targets unwanted weight by optimizing blood sugar levels. Formulated with natural ingredients, LeanBliss boasts effectiveness, efficiency, and, most importantly, safety in managing blood sugar levels while offering various associated health benefits. Official BUY LINKπŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡ https://leanbliss24.com/text.php#aff=Vivek5555 Packaged in chewable tablet form, each bottle of this weight loss and blood sugar-controlling supplement contains 30 tablets, ensuring the inclusion of vital ingredients necessary for its intended effects. With a focus on quality, LeanBliss is free from GMOs or stimulants that artificially induce health benefits. Additionally, its gluten-free and dairy-free composition underscores its safety for consumption. βœ…LeanBliss Ingredients: What Goes Into Its Making? The ingredients in the formulation of LeanBliss weight management aid have been informed to be natural by its manufacturer. When specifically looking into these, it has been noted that there exists a potential blend of exotic herbs, which are expected to provide the intended results when taken. These include the following: Ceylon Cinnamon Bark: It is needless to mention this type of cinnamon bark is native to Sri Lanka. Multiple health benefits are associated with this plant, one of which is reducing inflammatory response in the body. Since a majority of the inflammatory reactions are due to chronic health conditions, such as diabetes, arthritis, and heart disease, the cinnamaldehyde, an active component contained in the Ceylon cinnamon bark is what renders this plant its anti-inflammatory properties. The plant also helps enhance metabolism, which is essential in reducing weight. Corosolic Acid: A vital component present within the Banaba leaves from the tree of Banaba (scientific name: Lagerstroemia speciosa) found in Southeast Asia, Corosolic acid helps treat diabetes because of the antidiabetic properties contained within it. Meanwhile, it would be worth noting that every part of this plant is noted with some or other health benefits. For instance, its fruits and roots have been found to have analgesic properties. Citrus Sinensis: This ingredient in the LeanBliss formula is considered to be useful in weight loss for overweight people. It is alternatively termed as Sicilian blood orange, which is beneficial in tackling stubborn weight gain in people who are otherwise medically healthy. Notably, it is the anthocyanins and cyanidin 3-glucoside present in this orange that make it effective in reducing unwanted weight. Saffron Bulb Extract: Saffron which is often used as a spice is also bestowed with medicinal properties. The anticancer property of saffron helps prevent and treat cancer. The saffron bulb extract is also helpful in treating PMS symptoms in women, such as headaches, pain, irritability, and cravings. βœ…How Does The LeanBliss Formula Work? The LeanBliss weight loss support supplement operates by regulating blood sugar levels, thereby facilitating healthy weight loss. Given the prevalent issues of obesity and overweight in the United States, medical interventions for these conditions often come at considerable expense. Despite numerous attempts, such as restrictive diets, intense workouts, and starvation, many individuals struggle to shed unwanted weight. Official BUY LINKπŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡ https://leanbliss24.com/text.php#aff=Vivek5555 In response to these challenges, US physicians have sought to develop supplements that are natural, diet-friendly, and yield optimal results. LeanBliss, a fat-burning formula, emerges as a product of such efforts, purportedly created by a doctor and supported by robust clinical research and findings. Contrary to conventional beliefs, studies suggest that fluctuating blood sugar levels may precede weight gain, rather than vice versa. This revelation underscores the significance of pancreatic function, particularly insulin production and glucose utilization, in regulating hunger cravings and weight gain. Understanding this mechanism sheds light on how the LeanBliss dietary formula operates, offering insight into its design and functionality. Official BUY LINKπŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡πŸ‘‡ https://leanbliss24.com/text.php#aff=Vivek5555 #leanbliss #leanblissreview #leanblissreviews lean bliss,lean bliss review,lean bliss supplement review,lean bliss supplement,lean bliss weight loss,lean bliss lean bliss really works,does lean bliss work,lean bliss fda,weight loss lean bliss,lean bliss honest review,lean bliss weight loss supplement,lean bliss weight loss supplement review,leanbliss review,leanbliss reviews,leanbliss weight loss,leanbliss buy,lean bliss buy,leanbliss benefits,leanbliss ingredients,leanbliss order,lean bliss 2024 #weight #weightloss #fitness #health #healthylifestyle #healthyfood #fitnessm otivation #weightlossmotivation #training #food # #lifestyle#transformation #body #weightlossjourney bodybuilding #weightgain #weightwatchers #Supplements #Supplementshealth
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  • Simple and nutritious smoothie diet plan recipe:
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    Simple and nutritious smoothie diet plan recipe: Morning Kickstart Smoothie: Ingredients: 1 cup spinach,1 banana, 1/2 cup frozen berries (blueberries, strawberries, raspberries), 1/2 cup Greek yogurt, 1 tablespoon honey, 1/2 cup almond milk. Instructions: Blend all ingredients together until smooth. Enjoy as a refreshing breakfast or morning snack. Midday Boost Smoothie: Ingredients: 1 cup kale, 1/2 cup pineapple chunks, 1/2 cup cucumber slices, 1/2 avocadoJuice of , 1/2 lime, 1/2 cup coconut water. Instructions: Blend all ingredients until smooth. Pour into a glass and savor the rejuvenating flavors. Afternoon Refuel Smoothie: Ingredients: 1 cup spinach, 1/2 cup mango chunks, 1/2 cup pineapple chunks, 1/2 cup Greek yogurt, 1 tablespoon chia seeds, 1/2 cup water or coconut water. Instructions:Combine all ingredients in a blender. Blend until creamy and enjoy as a healthy pick-me-up. Evening Relaxation Smoothie: Ingredients: 1/2 cup kale, 1/2 cup cucumber slices, 1/2 avocado, 1/2 banana, 1 tablespoon almond butter, 1/2 cup almond milk, A dash of cinnamon (optional). Instructions:Blend all ingredients until smooth and creamy. Pour into a glass, sprinkle with cinnamon if desired, and unwind with this nourishing treat. Remember to drink plenty of water throughout the day and listen to your body's hunger cues. Enjoy your smoothie journey! And more click here to know πŸ‘‡ https://bit.ly/3UkMKHo #weightloss #weightlossjourney #fitness #healthylifestyle #motivation #health #healthy #workout #diet #fitnessmotivation #healthyfood #weightlosstransformation #gym #fit #nutrition #fitfam #fatloss #healthyeating #exercise #slimmingworld #weightlossmotivation #transformation #keto #bodybuilding #healthyliving #personaltrainer #lifestyle #food #fitnessjourney #training #smootheidietplan
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  • To loss more belly fate in only 21 days .
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  • Bill Gates and the UN impose their digital IDs on Sierra Leoneans.
    The West African nation of Sierra Leone is at full throttle with its digital transformation efforts, and its MOSIP-based foundational identity system is the nucleus of this project.
    https://expose-news.com/2024/04/13/bill-gates-and-un-impose-digital-ids/
    Bill Gates and the UN impose their digital IDs on Sierra Leoneans. The West African nation of Sierra Leone is at full throttle with its digital transformation efforts, and its MOSIP-based foundational identity system is the nucleus of this project. https://expose-news.com/2024/04/13/bill-gates-and-un-impose-digital-ids/
    EXPOSE-NEWS.COM
    Bill Gates and the UN impose their digital IDs on Sierra Leoneans
    The West African nation of Sierra Leone is at full throttle with its digital transformation efforts, and its MOSIP-based foundational identity system is the nucleus of this project. The Modular Ope…
    0 Comments 0 Shares 1630 Views
  • Pfizer partnering with Ido Bachelet on DNA nanorobots
    OUTRAGED HUMAN
    “No, no it’s not science fiction; it’s already happening,” said Ido Bachelet to a somewhat incredulous audience member








    https://www.youtube.com/watch?v=MzLTWU2EqP4 Ido Bachelet - Moonshot Thinking


    ... when they cause too much damage by mistake...

    or intentionally...


    5:12

    study your biology and activate targeted medication when necessary.


    5:36

    We also know how to remote-control these robots, using magnetic fields.

    5:40

    Furthermore, we can control them, as you saw in the clip, with a joystick,

    5:43

    directing them to a specific part of the body,

    5:46

    and then activating them with the push of a button.

    5:49

    We have also connected this joystick to the internet.

    5:51

    Our robots have a IP address,

    5:54

    so you can connect with them from afar and activate them online.



    6:01

    Imagine that in a couple of years,

    6:03

    your doctor will be able to sit at home with his smartphone,

    6:05

    and instead of playing "Candy Crush"

    6:08

    he will connect with the robots inside of you,

    6:11

    activate a certain medication and possibly even save you, just in time.

    AND IMAGINE THAT YOU WOULDN'T EVEN KNOW IT, YOU WOULDN'T BE TOLD ABOUT IT.

    AND THAT IN ORDER TO IMPLANT/INJECT IT, YOU WOULD BE TOLD THAT THERE IS A DREADFUL PANDEMIC, AND AT EVERY STEP YOU WOULD BE FORCED TO TAKE IT AS A NECESSARY "VACCINATION." AND A “PCR TEST”.

    BY YOUR GOVERNMENT, THE AIRLINES, THE EMPLOYER, THE WAITER AT THE RESTAURANT, THE FDA, THE EMA, THE WORLD HEALTH ORGANIZATION...

    AND YET IMAGINE THAT MANY PEOPLE WOULD DIE FROM IT, AND THEY WOULD BE YOUR RELATIVES AND FRIENDS.

    BUT YOU WOULD BE THE ONE WHO WOULD HAVE TO PROVE THAT IT WAS BECAUSE OF IT.

    IMAGINE BEING SURROUNDED BY CENSORSHIP, BEING RIDICULED, HAVING YOUR RIGHTS TO DO YOUR JOB, MOVE AROUND, OR EVEN SPEAK THE TRUTH AT ALL TAKEN AWAY FROM YOU....

    ISN’T THIS A BRIGHT FURTURE AND A FANTASTIC REALITY?

    ARE YOU AGAINST SCIENCE? AGAINST PROGRESS? AGAINST PREVENTING DISEASES?



    https://www.nextbigfuture.com/2015/05/pfizer-partnering-with-ido-bachelet-on.html

    Pfizer is cooperating with the DNA robot laboratory managed by Prof. Ido Bachelet at Bar-Ilan University. Bachelet has developed a method of producing innovative DNA molecules with characteristics that can be used to "program" them to reach specific locations in the body and carry out pre-programmed operations there in response to stimulation from the body. This cooperation was revealed in a lecture by Pfizer president of worldwide research and development (WRD), portfolio strategy and investment committee chairman, and executive VP Mikael Dolstein at the IATI Biomed Conference in Tel Aviv being concluded today.

    Research will focus on the possibility that the robots will deliver the medical proteins to designated tissue.

    Bachelet came to Bar-Ilan from the Massachusetts Institute of Technology (MIT) several years ago. At a Tedmed event held two years ago, he explained, "In order to make a nanometric robot, we first of all create a selected DNA sequence, and then fold it using a process called DNA origami. With this method, a person can give a command to a computer, which folds the DNA molecule as needed.

    "The result is that a DNA sequence can be made in the form of a clam, for example, and containing a drug. The DNA molecule, however, contains a code activated upon encountering certain materials in the body. For example, the clam can be designed to change its shape and release the drug only when it meets a cancer cell or the right tissue.

    "In addition, the molecules can receive signals from each other, and can theoretically change their shape according to signals from the body, and can be pre-programmed to attach themselves to one another. In the future, it will be possible to combine each such molecule with a miniature antenna. When the antenna receives an external signal, it will make a small change in the molecule that will make it open or close, and dissipate or connect itself to another molecule."



    In a brief talk, Bachelet said DNA nanobots will soon be tried in a critically ill leukemia patient. The patient, who has been given roughly six months to live, will receive an injection of DNA nanobots designed to interact with and destroy leukemia cells—while causing virtually zero collateral damage in healthy tissue.

    According to Bachelet, his team have successfully tested their method in cell cultures and animals and written two papers on the subject, one in Science and one in Nature.

    Contemporary cancer therapies involving invasive surgery and blasts of drugs can be as painful and damaging to the body as the disease itself. If Bachelet's approach proves successful in humans, and is backed by more research in the coming years, the team’s work could signal a transformational moment in cancer treatment.

    If this treatment works this will be a medical breakthrough and can be used for many other diseases by delivering drugs more effectively without causing side effects.

    2012 Video with answers from George Church, Ido Bachelet and Shawn Douglas on the medical DNA double helix clamshell nanobucket nanobot



    George Church indicates the smart DNA nanobot has applications beyond nanomedicine. Applications where there is any need for programmable and targeted release or interaction at the cellular or near molecular scale.

    2014 Geek Time Presentation from Ido Bachelet



    “AND THE LAST THING I AM GOING TO SCHOW YOU IS… PANDEMIC.

    SO, WE ARE REALLY CONCERNED ABOUT PANDEMICS… ESPECIALLY INFLUENZA PANDEMICS.

    SO THE BEST WAY TO AVOID PANDEMICS OR TO HANDLE PANDEMICS, IS SIMPLY TO KNOW WHERE THE VIRUS IS AND NOT TO BE THERE…

    IT SOUNDS STUPID, BUT IT IS ACTUALLY THE CASE…

    IF YOU COULD IDENTIFY WHERE THE VIRUS IS IN REAL TIME AND YOU CAN CONTAIN THAT AREA, YOU WOULD STOP THE PANDEMIC, YOU WOULD STOP THE DISEASE… OK?


    SO, WHAT WE DEVELOPED IS A SENSOR… COMPOSED OF CARBON NANOTUBES FUNCTIONALIZED WITH ALL KIND OF THINGS… THE SENSOR IS EXTREMELY SENSITIVE… WE’VE BUILT THIS APPLICATION… THEY SEND THEIR GPS COORDINATES TO OUR SERVER SO WE CAN SORT OF RECONSTRUCT A REAL MAP…

    I HOPE YOU ENJOYED THIS AND UNDESTOOND WHAT BIONICS IS ALL ABOUT…

    At the British Friends of Bar-Ilan University's event in Otto Uomo October 2014 Professor Ido Bachelet announced the beginning of the human treatment with nanomedicine. He indicates DNA nanobots can currently identify cells in humans with 12 different types of cancer tumors.

    A human patient with late stage leukemia will be given DNA nanobot treatment. Without the DNA nanobot treatment the patient would be expected to die in the summer of 2015. Based upon animal trials they expect to remove the cancer within one month.

    Within 1 or 2 years they hope to have spinal cord repair working in animals and then shortly thereafter in humans. This is working in tissue cultures.

    Previously Ido Bachelet and Shawn Douglas have published work on DNA nanobots in the journal Nature and other respected science publications.

    One Trillion 50 nanometer nanobots in a syringe will be injected into people to perform cellular surgery.

    The DNA nanobots have been tuned to not cause an immune response.
    They have been adjusted for different kinds of medical procedures. Procedures can be quick or ones that last many days.


    Medicine or treatment released based upon molecular sensing - Only targeted cells are treated

    Ido's daughter has a leg disease which requires frequent surgery. He is hoping his DNA nanobots will make the type of surgery she needs relatively trivial - a simple injection at a doctor's office.

    We can control powerful drugs that were already developed

    Effective drugs that were withdrawn from the market for excessive toxicity can be combined with DNA nanobots for effective delivery. The tiny molecular computers of the DNA nanobots can provide molecular selective control for powerful medicines that were already developed.

    Using DNA origami and molecular programming, they are reality. These nanobots can seek and kill cancer cells, mimic social insect behaviors, carry out logical operators like a computer in a living animal, and they can be controlled from an Xbox. Ido Bachelet from the bio-design lab at Bar Ilan University explains this technology and how it will change medicine in the near future.

    Ido Bachelet earned his Ph.D. from the Hebrew University in Jerusalem, and was a postdoctoral fellow at M.I.T. and Harvard University. He is currently an assistant professor in the Faculty of Life Sciences and the Nano-Center at Bar Ilan University, Israel, the founder of several biotech companies, and a composer of music for piano and molecules.


    Researchers have injected various kinds of DNA nanobots into cockroaches. Because the nanobots are labelled with fluorescent markers, the researchers can follow them and analyse how different robot combinations affect where substances are delivered. The team says the accuracy of delivery and control of the nanobots is equivalent to a computer system.

    This is the development of the vision of nanomedicine.
    This is the realization of the power of DNA nanotechnology.
    This is programmable dna nanotechnology.

    The DNA nanotechnology cannot perform atomically precise chemistry (yet), but having control of the DNA combined with advanced synthetic biology and control of proteins and nanoparticles is clearly developing into very interesting capabilities.

    "This is the first time that biological therapy has been able to match how a computer processor works," says co-author Ido Bachelet of the Institute of Nanotechnology and Advanced Materials at Bar Ilan University.

    The team says it should be possible to scale up the computing power in the cockroach to that of an 8-bit computer, equivalent to a Commodore 64 or Atari 800 from the 1980s. Goni-Moreno agrees that this is feasible. "The mechanism seems easy to scale up so the complexity of the computations will soon become higher," he says.

    An obvious benefit of this technology would be cancer treatments, because these must be cell-specific and current treatments are not well-targeted. But a treatment like this in mammals must overcome the immune response triggered when a foreign object enters the body.

    Bachelet is confident that the team can enhance the robots' stability so that they can survive in mammals. "There is no reason why preliminary trials on humans can't start within five years," he says

    Biological systems are collections of discrete molecular objects that move around and collide with each other. Cells carry out elaborate processes by precisely controlling these collisions, but developing artificial machines that can interface with and control such interactions remains a significant challenge. DNA is a natural substrate for computing and has been used to implement a diverse set of mathematical problems, logic circuits and robotics. The molecule also interfaces naturally with living systems, and different forms of DNA-based biocomputing have already been demonstrated. Here, we show that DNA origami can be used to fabricate nanoscale robots that are capable of dynamically interacting with each other in a living animal. The interactions generate logical outputs, which are relayed to switch molecular payloads on or off. As a proof of principle, we use the system to create architectures that emulate various logic gates (AND, OR, XOR, NAND, NOT, CNOT and a half adder). Following an ex vivo prototyping phase, we successfully used the DNA origami robots in living cockroaches (Blaberus discoidalis) to control a molecule that targets their cells.

    Nature Nanotechnology - Universal computing by DNA origami robots in a living animal


    44 pages of supplemental information

    Ido Bachelet's moonshot to use nanorobotics for surgery has the potential to change lives globally. But who is the man behind the moonshot?

    Ido graduated from the Hebrew University of Jerusalem with a PhD in pharmacology and experimental therapeutics. Afterwards he did two postdocs; one in engineering at MIT and one in synthetic biology in the lab of George Church at the Wyss Institute at Harvard.

    Now, his group at Bar-Ilan University designs and studies diverse technologies inspired by nature.

    They will deliver enzymes that break down cells via programmable nanoparticles.
    Delivering insulin to tell cells to grow and regenerate tissue at the desired location.
    Surgery would be performed by putting the programmable nanoparticles into saline and injecting them into the body to seek out remove bad cells and grow new cells and perform other medical work.


    Research group website is here.












    SOLVE FOR DISEASE X?

    https://en.globes.co.il/en/article-pfizer-to-collaborate-on-bar-ilan-dna-robots-1001036703


    Pfizer is cooperating with the DNA robot laboratory managed by Prof. Ido Bachelet at Bar-Ilan University. Bachelet has developed a method of producing innovative DNA molecules with characteristics that can be used to "program" them to reach specific locations in the body and carry out pre-programmed operations there in response to stimulation from the body. This cooperation was revealed in a lecture by Pfizer president of worldwide research and development (WRD), portfolio strategy and investment committee chairman, and executive VP Mikael Dolstein at the IATI Biomed Conference in Tel Aviv being concluded today.

    Bar-Ilan Research & Development Co. CEO Orli Tori said, "This is Pfizer's first cooperative venture with someone in Israeli higher education. The technology is fairly new for a drug company, but Pfizer has agreed to take up the challenge and support this technology, in the hope that it will make a contribution to the company at the proper time.

    "As in all of our research agreements, the company coming from the industry has the right to negotiate the acquisition of the technology at the end of the process." The financial volume of the deal was not disclosed, but most such agreements amount to several hundred thousand dollars at most. The medical sector in which cooperation will take place was also not disclosed,

    but it appears that research will focus on the possibility that the robots will deliver the medical proteins to designated tissue.

    Bachelet came to Bar-Ilan from the Massachusetts Institute of Technology (MIT) several years ago. At a Tedmed event held two years ago, he explained, "In order to make a nanometric robot, we first of all create a selected DNA sequence, and then fold it using a process called DNA origami. With this method, a person can give a command to a computer, which folds the DNA molecule as needed.

    "The result is that a DNA sequence can be made in the form of a clam, for example, and containing a drug. The DNA molecule, however, contains a code activated upon encountering certain materials in the body. For example, the clam can be designed to change its shape and release the drug only when it meets a cancer cell or the right tissue.

    "In addition, the molecules can receive signals from each other, and can theoretically change their shape according to signals from the body, and can be pre-programmed to attach themselves to one another. In the future, it will be possible to combine each such molecule with a miniature antenna.

    When the antenna receives an external signal, it will make a small change in the molecule that will make it open or close, and dissipate or connect itself to another molecule."

    Tori adds, "What is special about the robots is that they open and close according to signals from the surroundings, and that makes it possible to manage the disease. The robot exposes the drug to the target site according to biological signs within the body. For example were we to develop a product for diabetes, although that is not the purpose of this cooperation, it would be possible to develop a robot that would release insulin only when it sensed a rise in the blood sugar level."

    Published by Globes [online], Israel business news - www.globes-online.com - on May 14, 2015

    https://www.nextbigfuture.com/2015/03/ido-bachelet-dna-nanobots-summary-with.html

    Disadvantages

    1. Designing of nanorobot is very costly and complicated

    2. Stray field might be created from electrical systems which can trigger bioelectric based molecular recognition system in biology

    3. Electrical nanorobots remain vulnerable to electrical interference from other sources like radiofrequency or electric fields, electromagnetic pulse and stray fields from other in-vivo electronic devices.

    4. Nanorobots are difficult to design, and customize

    5. These are capable of molecular level destruction of human body thus it can cause terrible effect in terrorism field. Terrorist may make usage of nanorobots as a tool for torturing opponent community

    6. Other possible threat associated with nanorobots is privacy issue.

    As it dealt with designing of miniature form of devices, there are risks for snooping than that exist already.

    [https://web.archive.org/web/20200718043030/https://pharmascope.org/ijrps/article/download/2523/5031]

    [https://web.archive.org/web/20150911233849/http://www.nanosafe.org/home/liblocal/docs/Nanosafe%202014/Session%201/PL1%20-%20Fran%C3%A7ois%20TARDIF.pdf]

    NANOROBOTS:

    SOCIETAL CONCERNS: INDIVIDUAL FREEDOM, TRANSHUMANISM!!!

    http://immortality-roadmap.com/nanorisk.pdf










    http://jddtonline.info/index.php/jddt/article/download/891/533

    There are several drawbacks with this technology like toxicity, contamination. Sometime human body generates strong immune response against them.

    https://web.archive.org/web/20051218111931/http://teknologiskfremsyn.dk:80/download/58.pdf


    “Nanotubes can be highly toxic”

    Fifteen percent of the rats treated with carbon nanotubes suffocated to death within twenty-four hours due to clumping of the nanotubes that obstructed the bronchial passageways.








    Toxicity- the issue of toxicity of nanoparticles was raised as an area in which more research is needed, particularly in terms of whether the regulatory system is sufficient.






    And it's injected into people, soldiers, children, even infants…

    Thank you Zz for this link.



    Pfizer partnering with Ido Bachelet on DNA nano robots.

    “No, no it’s not science fiction; it’s already happening,” said Ido Bachelet to a somewhat incredulous audience member, displaying a test tube in which he says just one drop contains approximately 1,000 billiard robots.

    https://outraged.substack.com/p/pfizer-partnering-with-ido-bachelet?utm_source=cross-post&publication_id=1087020&post_id=143153580&utm_campaign=956088&isFreemail=true&r=1sq9d8&triedRedirect=true&utm_medium=email

    Follow @zeeemedia
    Website | X | Instagram | Rumble

    https://telegra.ph/Pfizer-partnering-with-Ido-Bachelet-on-DNA-nanorobots-04-03
    Pfizer partnering with Ido Bachelet on DNA nanorobots OUTRAGED HUMAN “No, no it’s not science fiction; it’s already happening,” said Ido Bachelet to a somewhat incredulous audience member https://www.youtube.com/watch?v=MzLTWU2EqP4 Ido Bachelet - Moonshot Thinking ... when they cause too much damage by mistake... or intentionally... 5:12 study your biology and activate targeted medication when necessary. 5:36 We also know how to remote-control these robots, using magnetic fields. 5:40 Furthermore, we can control them, as you saw in the clip, with a joystick, 5:43 directing them to a specific part of the body, 5:46 and then activating them with the push of a button. 5:49 We have also connected this joystick to the internet. 5:51 Our robots have a IP address, 5:54 so you can connect with them from afar and activate them online. 6:01 Imagine that in a couple of years, 6:03 your doctor will be able to sit at home with his smartphone, 6:05 and instead of playing "Candy Crush" 6:08 he will connect with the robots inside of you, 6:11 activate a certain medication and possibly even save you, just in time. AND IMAGINE THAT YOU WOULDN'T EVEN KNOW IT, YOU WOULDN'T BE TOLD ABOUT IT. AND THAT IN ORDER TO IMPLANT/INJECT IT, YOU WOULD BE TOLD THAT THERE IS A DREADFUL PANDEMIC, AND AT EVERY STEP YOU WOULD BE FORCED TO TAKE IT AS A NECESSARY "VACCINATION." AND A “PCR TEST”. BY YOUR GOVERNMENT, THE AIRLINES, THE EMPLOYER, THE WAITER AT THE RESTAURANT, THE FDA, THE EMA, THE WORLD HEALTH ORGANIZATION... AND YET IMAGINE THAT MANY PEOPLE WOULD DIE FROM IT, AND THEY WOULD BE YOUR RELATIVES AND FRIENDS. BUT YOU WOULD BE THE ONE WHO WOULD HAVE TO PROVE THAT IT WAS BECAUSE OF IT. IMAGINE BEING SURROUNDED BY CENSORSHIP, BEING RIDICULED, HAVING YOUR RIGHTS TO DO YOUR JOB, MOVE AROUND, OR EVEN SPEAK THE TRUTH AT ALL TAKEN AWAY FROM YOU.... ISN’T THIS A BRIGHT FURTURE AND A FANTASTIC REALITY? ARE YOU AGAINST SCIENCE? AGAINST PROGRESS? AGAINST PREVENTING DISEASES? https://www.nextbigfuture.com/2015/05/pfizer-partnering-with-ido-bachelet-on.html Pfizer is cooperating with the DNA robot laboratory managed by Prof. Ido Bachelet at Bar-Ilan University. Bachelet has developed a method of producing innovative DNA molecules with characteristics that can be used to "program" them to reach specific locations in the body and carry out pre-programmed operations there in response to stimulation from the body. This cooperation was revealed in a lecture by Pfizer president of worldwide research and development (WRD), portfolio strategy and investment committee chairman, and executive VP Mikael Dolstein at the IATI Biomed Conference in Tel Aviv being concluded today. Research will focus on the possibility that the robots will deliver the medical proteins to designated tissue. Bachelet came to Bar-Ilan from the Massachusetts Institute of Technology (MIT) several years ago. At a Tedmed event held two years ago, he explained, "In order to make a nanometric robot, we first of all create a selected DNA sequence, and then fold it using a process called DNA origami. With this method, a person can give a command to a computer, which folds the DNA molecule as needed. "The result is that a DNA sequence can be made in the form of a clam, for example, and containing a drug. The DNA molecule, however, contains a code activated upon encountering certain materials in the body. For example, the clam can be designed to change its shape and release the drug only when it meets a cancer cell or the right tissue. "In addition, the molecules can receive signals from each other, and can theoretically change their shape according to signals from the body, and can be pre-programmed to attach themselves to one another. In the future, it will be possible to combine each such molecule with a miniature antenna. When the antenna receives an external signal, it will make a small change in the molecule that will make it open or close, and dissipate or connect itself to another molecule." In a brief talk, Bachelet said DNA nanobots will soon be tried in a critically ill leukemia patient. The patient, who has been given roughly six months to live, will receive an injection of DNA nanobots designed to interact with and destroy leukemia cells—while causing virtually zero collateral damage in healthy tissue. According to Bachelet, his team have successfully tested their method in cell cultures and animals and written two papers on the subject, one in Science and one in Nature. Contemporary cancer therapies involving invasive surgery and blasts of drugs can be as painful and damaging to the body as the disease itself. If Bachelet's approach proves successful in humans, and is backed by more research in the coming years, the team’s work could signal a transformational moment in cancer treatment. If this treatment works this will be a medical breakthrough and can be used for many other diseases by delivering drugs more effectively without causing side effects. 2012 Video with answers from George Church, Ido Bachelet and Shawn Douglas on the medical DNA double helix clamshell nanobucket nanobot George Church indicates the smart DNA nanobot has applications beyond nanomedicine. Applications where there is any need for programmable and targeted release or interaction at the cellular or near molecular scale. 2014 Geek Time Presentation from Ido Bachelet “AND THE LAST THING I AM GOING TO SCHOW YOU IS… PANDEMIC. SO, WE ARE REALLY CONCERNED ABOUT PANDEMICS… ESPECIALLY INFLUENZA PANDEMICS. SO THE BEST WAY TO AVOID PANDEMICS OR TO HANDLE PANDEMICS, IS SIMPLY TO KNOW WHERE THE VIRUS IS AND NOT TO BE THERE… IT SOUNDS STUPID, BUT IT IS ACTUALLY THE CASE… IF YOU COULD IDENTIFY WHERE THE VIRUS IS IN REAL TIME AND YOU CAN CONTAIN THAT AREA, YOU WOULD STOP THE PANDEMIC, YOU WOULD STOP THE DISEASE… OK? SO, WHAT WE DEVELOPED IS A SENSOR… COMPOSED OF CARBON NANOTUBES FUNCTIONALIZED WITH ALL KIND OF THINGS… THE SENSOR IS EXTREMELY SENSITIVE… WE’VE BUILT THIS APPLICATION… THEY SEND THEIR GPS COORDINATES TO OUR SERVER SO WE CAN SORT OF RECONSTRUCT A REAL MAP… I HOPE YOU ENJOYED THIS AND UNDESTOOND WHAT BIONICS IS ALL ABOUT… At the British Friends of Bar-Ilan University's event in Otto Uomo October 2014 Professor Ido Bachelet announced the beginning of the human treatment with nanomedicine. He indicates DNA nanobots can currently identify cells in humans with 12 different types of cancer tumors. A human patient with late stage leukemia will be given DNA nanobot treatment. Without the DNA nanobot treatment the patient would be expected to die in the summer of 2015. Based upon animal trials they expect to remove the cancer within one month. Within 1 or 2 years they hope to have spinal cord repair working in animals and then shortly thereafter in humans. This is working in tissue cultures. Previously Ido Bachelet and Shawn Douglas have published work on DNA nanobots in the journal Nature and other respected science publications. One Trillion 50 nanometer nanobots in a syringe will be injected into people to perform cellular surgery. The DNA nanobots have been tuned to not cause an immune response. They have been adjusted for different kinds of medical procedures. Procedures can be quick or ones that last many days. Medicine or treatment released based upon molecular sensing - Only targeted cells are treated Ido's daughter has a leg disease which requires frequent surgery. He is hoping his DNA nanobots will make the type of surgery she needs relatively trivial - a simple injection at a doctor's office. We can control powerful drugs that were already developed Effective drugs that were withdrawn from the market for excessive toxicity can be combined with DNA nanobots for effective delivery. The tiny molecular computers of the DNA nanobots can provide molecular selective control for powerful medicines that were already developed. Using DNA origami and molecular programming, they are reality. These nanobots can seek and kill cancer cells, mimic social insect behaviors, carry out logical operators like a computer in a living animal, and they can be controlled from an Xbox. Ido Bachelet from the bio-design lab at Bar Ilan University explains this technology and how it will change medicine in the near future. Ido Bachelet earned his Ph.D. from the Hebrew University in Jerusalem, and was a postdoctoral fellow at M.I.T. and Harvard University. He is currently an assistant professor in the Faculty of Life Sciences and the Nano-Center at Bar Ilan University, Israel, the founder of several biotech companies, and a composer of music for piano and molecules. Researchers have injected various kinds of DNA nanobots into cockroaches. Because the nanobots are labelled with fluorescent markers, the researchers can follow them and analyse how different robot combinations affect where substances are delivered. The team says the accuracy of delivery and control of the nanobots is equivalent to a computer system. This is the development of the vision of nanomedicine. This is the realization of the power of DNA nanotechnology. This is programmable dna nanotechnology. The DNA nanotechnology cannot perform atomically precise chemistry (yet), but having control of the DNA combined with advanced synthetic biology and control of proteins and nanoparticles is clearly developing into very interesting capabilities. "This is the first time that biological therapy has been able to match how a computer processor works," says co-author Ido Bachelet of the Institute of Nanotechnology and Advanced Materials at Bar Ilan University. The team says it should be possible to scale up the computing power in the cockroach to that of an 8-bit computer, equivalent to a Commodore 64 or Atari 800 from the 1980s. Goni-Moreno agrees that this is feasible. "The mechanism seems easy to scale up so the complexity of the computations will soon become higher," he says. An obvious benefit of this technology would be cancer treatments, because these must be cell-specific and current treatments are not well-targeted. But a treatment like this in mammals must overcome the immune response triggered when a foreign object enters the body. Bachelet is confident that the team can enhance the robots' stability so that they can survive in mammals. "There is no reason why preliminary trials on humans can't start within five years," he says Biological systems are collections of discrete molecular objects that move around and collide with each other. Cells carry out elaborate processes by precisely controlling these collisions, but developing artificial machines that can interface with and control such interactions remains a significant challenge. DNA is a natural substrate for computing and has been used to implement a diverse set of mathematical problems, logic circuits and robotics. The molecule also interfaces naturally with living systems, and different forms of DNA-based biocomputing have already been demonstrated. Here, we show that DNA origami can be used to fabricate nanoscale robots that are capable of dynamically interacting with each other in a living animal. The interactions generate logical outputs, which are relayed to switch molecular payloads on or off. As a proof of principle, we use the system to create architectures that emulate various logic gates (AND, OR, XOR, NAND, NOT, CNOT and a half adder). Following an ex vivo prototyping phase, we successfully used the DNA origami robots in living cockroaches (Blaberus discoidalis) to control a molecule that targets their cells. Nature Nanotechnology - Universal computing by DNA origami robots in a living animal 44 pages of supplemental information Ido Bachelet's moonshot to use nanorobotics for surgery has the potential to change lives globally. But who is the man behind the moonshot? Ido graduated from the Hebrew University of Jerusalem with a PhD in pharmacology and experimental therapeutics. Afterwards he did two postdocs; one in engineering at MIT and one in synthetic biology in the lab of George Church at the Wyss Institute at Harvard. Now, his group at Bar-Ilan University designs and studies diverse technologies inspired by nature. They will deliver enzymes that break down cells via programmable nanoparticles. Delivering insulin to tell cells to grow and regenerate tissue at the desired location. Surgery would be performed by putting the programmable nanoparticles into saline and injecting them into the body to seek out remove bad cells and grow new cells and perform other medical work. Research group website is here. SOLVE FOR DISEASE X? https://en.globes.co.il/en/article-pfizer-to-collaborate-on-bar-ilan-dna-robots-1001036703 Pfizer is cooperating with the DNA robot laboratory managed by Prof. Ido Bachelet at Bar-Ilan University. Bachelet has developed a method of producing innovative DNA molecules with characteristics that can be used to "program" them to reach specific locations in the body and carry out pre-programmed operations there in response to stimulation from the body. This cooperation was revealed in a lecture by Pfizer president of worldwide research and development (WRD), portfolio strategy and investment committee chairman, and executive VP Mikael Dolstein at the IATI Biomed Conference in Tel Aviv being concluded today. Bar-Ilan Research & Development Co. CEO Orli Tori said, "This is Pfizer's first cooperative venture with someone in Israeli higher education. The technology is fairly new for a drug company, but Pfizer has agreed to take up the challenge and support this technology, in the hope that it will make a contribution to the company at the proper time. "As in all of our research agreements, the company coming from the industry has the right to negotiate the acquisition of the technology at the end of the process." The financial volume of the deal was not disclosed, but most such agreements amount to several hundred thousand dollars at most. The medical sector in which cooperation will take place was also not disclosed, but it appears that research will focus on the possibility that the robots will deliver the medical proteins to designated tissue. Bachelet came to Bar-Ilan from the Massachusetts Institute of Technology (MIT) several years ago. At a Tedmed event held two years ago, he explained, "In order to make a nanometric robot, we first of all create a selected DNA sequence, and then fold it using a process called DNA origami. With this method, a person can give a command to a computer, which folds the DNA molecule as needed. "The result is that a DNA sequence can be made in the form of a clam, for example, and containing a drug. The DNA molecule, however, contains a code activated upon encountering certain materials in the body. For example, the clam can be designed to change its shape and release the drug only when it meets a cancer cell or the right tissue. "In addition, the molecules can receive signals from each other, and can theoretically change their shape according to signals from the body, and can be pre-programmed to attach themselves to one another. In the future, it will be possible to combine each such molecule with a miniature antenna. When the antenna receives an external signal, it will make a small change in the molecule that will make it open or close, and dissipate or connect itself to another molecule." Tori adds, "What is special about the robots is that they open and close according to signals from the surroundings, and that makes it possible to manage the disease. The robot exposes the drug to the target site according to biological signs within the body. For example were we to develop a product for diabetes, although that is not the purpose of this cooperation, it would be possible to develop a robot that would release insulin only when it sensed a rise in the blood sugar level." Published by Globes [online], Israel business news - www.globes-online.com - on May 14, 2015 https://www.nextbigfuture.com/2015/03/ido-bachelet-dna-nanobots-summary-with.html Disadvantages 1. Designing of nanorobot is very costly and complicated 2. Stray field might be created from electrical systems which can trigger bioelectric based molecular recognition system in biology 3. Electrical nanorobots remain vulnerable to electrical interference from other sources like radiofrequency or electric fields, electromagnetic pulse and stray fields from other in-vivo electronic devices. 4. Nanorobots are difficult to design, and customize 5. These are capable of molecular level destruction of human body thus it can cause terrible effect in terrorism field. Terrorist may make usage of nanorobots as a tool for torturing opponent community 6. Other possible threat associated with nanorobots is privacy issue. As it dealt with designing of miniature form of devices, there are risks for snooping than that exist already. [https://web.archive.org/web/20200718043030/https://pharmascope.org/ijrps/article/download/2523/5031] [https://web.archive.org/web/20150911233849/http://www.nanosafe.org/home/liblocal/docs/Nanosafe%202014/Session%201/PL1%20-%20Fran%C3%A7ois%20TARDIF.pdf] NANOROBOTS: SOCIETAL CONCERNS: INDIVIDUAL FREEDOM, TRANSHUMANISM!!! http://immortality-roadmap.com/nanorisk.pdf http://jddtonline.info/index.php/jddt/article/download/891/533 There are several drawbacks with this technology like toxicity, contamination. Sometime human body generates strong immune response against them. https://web.archive.org/web/20051218111931/http://teknologiskfremsyn.dk:80/download/58.pdf “Nanotubes can be highly toxic” Fifteen percent of the rats treated with carbon nanotubes suffocated to death within twenty-four hours due to clumping of the nanotubes that obstructed the bronchial passageways. Toxicity- the issue of toxicity of nanoparticles was raised as an area in which more research is needed, particularly in terms of whether the regulatory system is sufficient. … And it's injected into people, soldiers, children, even infants… Thank you Zz for this link. Pfizer partnering with Ido Bachelet on DNA nano robots. “No, no it’s not science fiction; it’s already happening,” said Ido Bachelet to a somewhat incredulous audience member, displaying a test tube in which he says just one drop contains approximately 1,000 billiard robots. https://outraged.substack.com/p/pfizer-partnering-with-ido-bachelet?utm_source=cross-post&publication_id=1087020&post_id=143153580&utm_campaign=956088&isFreemail=true&r=1sq9d8&triedRedirect=true&utm_medium=email Follow @zeeemedia Website | X | Instagram | Rumble https://telegra.ph/Pfizer-partnering-with-Ido-Bachelet-on-DNA-nanorobots-04-03
    OUTRAGED.SUBSTACK.COM
    Pfizer partnering with Ido Bachelet on DNA nanorobots
    “No, no it’s not science fiction; it’s already happening,” said Ido Bachelet to a somewhat incredulous audience member Thanks for reading OUTRAGED’s Newsletter! Subscribe for free to receive new posts and support my work. https://www.youtube.com/watch?v=MzLTWU2EqP4
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  • Pre-emptive Nuclear War: The Role of Israel in Triggering an Attack on Iran
    Chapter III of "The Globalization of War" by Michel Chossudovsky


    Firmly All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name.

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    Author’s Introduction and Update

    In a recent article entitled “A Planned US-Israeli Attack on Iran is Contemplated” I focussed on how Israel’s criminal attack on the People of Palestine could evolve towards an extended Middle East War.

    At the time of writing, US-NATO war ships –including two aircraft carriers, combat planes, not to mention a nuclear submarine– are deployed in the Eastern Mediterranean and the Red Sea, all of which are intended to confront what both Western politicians and the media casually describe as “Palestine’s Aggression against the Jewish State”.

    “Israel ranks” as “the 4th strongest military” after Russia, the U.S and China. Ask yourself: Why on earth would Israel need the support of U.S. aircraft carriers to lead a genocide against the Palestinians who are fighting for their lives with limited military capabilities.

    Is the U.S. intent upon triggering a broader war?

    “U.S. Warns Hezbollah, Iran. It Will intervene if they Escalate”

    Who is “Escalating”? The Pentagon has already intimated that it will attack Iran and Lebanon, “If they Escalate”. Is the Pentagon Seeking to Trigger one or more “False Flags”?



    Times of Israel, November 9, 2023

    Also of significance (less than 4 months prior to October 7, 2023) is the adoption on June 27, 2023 of the US Congress Resolution (H. RES. 559) which Accuses Iran of Possessing Nuclear Weapons. H.RES 559 allows the use of force against Iran, intimating that Iran has Nuclear Weapons.

    Whereas Iran is tagged (without a shred of evidence) as a Nuclear Power by the U.S. Congress, Washington fails to acknowledge that Israel is an undeclared nuclear power.





    The article below was first published in my book entitled “The Globalization of War. America’s Long War against Humanity” (2015).

    I remain indebted to the former Prime Minister of Malaysia Tun Dr. Mahathir Mohamad who took the initiative of launching my book in Kuala Lumpur. (image right).

    Firmly committed to “the criminalization of war”, Tun Mahathir is a powerful voice in support of Palestine.

    The article below (Chapter III of “Globalization of War”) provides analysis in a historical perspective of U.S. war plans directed against Iran.

    Numerous “war theater scenarios” for an all-out attack on Iran have been contemplated.

    Dangerous Crossroads in our History

    The current and ongoing US-NATO military deployment in The Middle East — casually presented by the media as a means to coming to the rescue of Israel– is the pinnacle of U.S. war preparations extending over a period of more than 20 years.

    Contemplated by the Pentagon in 2005 was a scenario whereby an attack by Israel would be conducted on behalf of Washington:

    “An attack by Israel could, however, be used as “the trigger mechanism” which would unleash an all-out war against Iran, as well as retaliation by Iran directed against Israel.” (quoted from text below)

    At the outset of Bush’s second term

    “Vice President Dick Cheney had hinted, in no uncertain terms, that Iran was “right at the top of the list” of the “rogue enemies” of America, and that Israel would, so to speak, “be doing the bombing for us” (Ibid)

    The article also focusses on the dangers of a US-Israel nuclear attack against Iran which has been contemplated by the Pentagon since 2004.

    The US Israel “Partnership”: “Signed” Military Agreement

    Amply documented, the U.S. Military and Intelligence apparatus is firmly behind Israel’s genocide. In the words of Lt General Richard Clark:

    Americans Troops are “prepared to die for the Jewish State”.

    What should be understood by this statement is that the US and Israel have a longstanding Military “Partnership” as well as (Jerusalem Post) a “Signed” Military Agreement (classified) regarding Israel’s attack on Gaza.

    Lt. General Richard Clark is U.S. Third Air Force Commander, among the highest-ranking military officers in the U.S. Armed Forces. While he refers to Juniper Cobra, “a joint military exercise that has been conducted for almost a decade”, his statement points to a much broader “signed” military-intelligence agreement (classified) with Israel which no doubt includes the extension of the Israeli-US bombing of Gaza to the broader Middle East.

    While this so-called “signed” military agreement remains classified (not in the public domain), it would appear that Biden is obeying the orders of the perpetrators of this diabolical military agenda.

    Does President Biden have the authority (under this “Signed” Agreement with Israel) to save the lives of innocent civilians including the children of Palestine:

    Q (Inaudible) Gaza ceasefire, Mr. President?

    THE PRESIDENT: Pardon me?

    Q What are the chances of a Gaza ceasefire?

    THE PRESIDENT: None. No possibility.

    White House Press Conference, November 9, 2023

    Lt. General Clark confirms that:

    “U.S. troops could be put under Israeli commanders in the battlefield”, which suggests that the genocide is implemented by Netanyahu on behalf of the United States.

    Everything indicates that the US military and intelligence apparatus are behind Israel’s criminal bombing and invasion of Gaza.

    We stand firmly in Solidarity with Palestine and the People of the Middle East.

    It is my intent and sincere hope that my writings (including the text below) will contribute to “Revealing the Truth” as well “Reversing the Tide of Global Warfare”.

    Michel Chossudovsky, Global Research, November 17, 2023, March 10, 2024

    Pre-emptive Nuclear War:

    The Role of Israel in Triggering an Attack on Iran

    by

    Michel Chossudovsky



    Introduction

    While one can conceptualize the loss of life and destruction resulting from present-day wars including Iraq and Afghanistan, it is impossible to fully comprehend the devastation which might result from a Third World War, using “new technologies” and advanced weapons, until it occurs and becomes a reality.

    The international community has endorsed nuclear war in the name of world peace. “Making the world safer” is the justification for launching a military operation which could potentially result in a nuclear holocaust.”

    The stockpiling and deployment of advanced weapons systems directed against Iran started in the immediate wake of the 2003 bombing and invasion of Iraq. From the outset, these war plans were led by the U.S. in liaison with NATO and Israel.

    Following the 2003 invasion of Iraq, the Bush administration identified Iran and Syria as the next stage of “the road map to war”. U.S. military sources intimated at the time that an aerial attack on Iran could involve a large scale deployment comparable to the U.S. “shock and awe” bombing raids on Iraq in March 2003:

    American air strikes on Iran would vastly exceed the scope of the 1981 Israeli attack on the Osiraq nuclear center in Iraq, and would more resemble the opening days of the 2003 air campaign against Iraq.1

    “Theater Iran Near Term” (TIRANNT)

    Code named by U.S. military planners as TIRANNT, “Theater Iran Near Term”, simulations of an attack on Iran were initiated in May 2003 “when modelers and intelligence specialists pulled together the data needed for theater-level (meaning large-scale) scenario analysis for Iran.”2

    The scenarios identified several thousand targets inside Iran as part of a “Shock and Awe” Blitzkrieg:

    The analysis, called TIRANNT, for “Theater Iran Near Term,” was coupled with a mock scenario for a Marine Corps invasion and a simulation of the Iranian missile force. U.S. and British planners conducted a Caspian Sea war game around the same time. And Bush directed the U.S. Strategic Command to draw up a global strike war plan for an attack against Iranian weapons of mass destruction. All of this will ultimately feed into a new war plan for “major combat operations” against Iran that military sources confirm now [April 2006] exists in draft form.

    … Under TIRANNT, Army and U.S. Central Command planners have been examining both near-term and out-year scenarios for war with Iran, including all aspects of a major combat operation, from mobilization and deployment of forces through postwar stability operations after regime change.3

    Different “theater scenarios” for an all-out attack on Iran had been contemplated:

    The U.S. army, navy, air force and marines have all prepared battle plans and spent four years building bases and training for “Operation Iranian Freedom”. Admiral Fallon, the new head of U.S. Central Command, has inherited computerized plans under the name TIRANNT (Theatre Iran Near Term).4

    In 2004, drawing upon the initial war scenarios under TIRANNT, Vice President Dick Cheney instructed U.S. Strategic Command (U.S.STRATCOM) to draw up a “contingency plan” of a large scale military operation directed against Iran “to be employed in response to another 9/11-type terrorist attack on the United States” on the presumption that the government in Tehran would be behind the terrorist plot. The plan included the pre-emptive use of nuclear weapons against a non-nuclear state:

    The plan includes a large-scale air assault on Iran employing both conventional and tactical nuclear weapons. Within Iran there are more than four hundred fifty major strategic targets, including numerous suspected nuclear-weapons-program develop- ment sites. Many of the targets are hardened or are deep underground and could not be taken out by conventional weapons, hence the nuclear option. As in the case of Iraq, the response is not conditional on Iran actually being involved in the act of ter- rorism directed against the United States. Several senior Air Force officers involved in the planning are reportedly appalled at the implications of what they are doing –that Iran is being set up for an unprovoked nuclear attack– but no one is prepared to dam- age his career by posing any objections.5

    The Military Road Map: “First Iraq, then Iran”

    The decision to target Iran under TIRANNT was part of the broader process of military planning and sequencing of military operations. Already under the Clinton administration (1995), U.S. Central Command (U.S.CENTCOM) had formulated “in war theater plans” to invade first Iraq and then Iran. Access to Middle East oil was the stated strategic objective:

    The broad national security interests and objectives expressed in the President’s National Security Strategy (NSS) and the Chairman’s National Military Strategy (NMS) form the foundation of the United States Central Command’s theater strategy. The NSS directs implementation of a strategy of dual containment of the rogue states of Iraq and Iran as long as those states pose a threat to U.S. interests, to other states in the region, and to their own citizens. Dual containment is designed to maintain the balance of power in the region without depending on either Iraq or Iran. U.S.CENTCOM’s theater strategy is interest-based and threat-focused. The purpose of U.S. engagement, as espoused in the NSS, is to protect the United States’ vital interest in the region – uninterrupted, secure U.S./Allied access to Gulf oil.6

    The war on Iran was viewed as part of a succession of military operations. According to (former) NATO Commander General Wesley Clark, the Pentagon’s military road-map consisted of a sequence of countries:

    [The] Five-year campaign plan [includes]… a total of seven countries, beginning with Iraq, then Syria, Lebanon, Libya, Iran, Somalia and Sudan.6 (For further details, see Chapter I)

    The Role of Israel

    There has been much debate regarding the role of Israel in initiating an attack against Iran.

    Israel is part of a military alliance. Tel Aviv is not a prime mover. It does not have a separate and distinct military agenda.

    Israel is integrated into the “war plan for major combat operations” against Iran formulated in 2006 by U.S. Strategic Command (U.S.STRATCOM). In the context of large scale military operations, an uncoordinated unilateral military action by one coalition partner, namely Israel, is from a military and strategic point almost an impossibility. Israel is a de facto member of NATO. Any action by Israel would require a “green light” from Washington.

    An attack by Israel could, however, be used as “the trigger mechanism” which would unleash an all-out war against Iran, as well as retaliation by Iran directed against Israel.

    In this regard, there are indications going back to the Bush administration that Washington had indeed contemplated the option of an initial (U.S. backed) attack by Israel rather than an outright U.S.-led military operation directed against Iran.

    The Israeli attack –although led in close liaison with the Pentagon and NATO– would have been presented to public opinion as a unilateral decision by Tel Aviv. It would then have been used by Washington to justify, in the eyes of World opinion, a military intervention of the U.S. and NATO with a view to “defending Israel”, rather than attacking Iran. Under existing military cooperation agreements, both the U.S. and NATO would be “obligated” to “defend Israel” against Iran and Syria.

    It is worth noting, in this regard, that at the outset of Bush’s second term, (former) Vice President Dick Cheney had hinted, in no uncertain terms, that Iran was “right at the top of the list” of the “rogue enemies” of America, and that Israel would, so to speak, “be doing the bombing for us”, without U.S. military involvement and without us putting pressure on them “to do it.”8

    According to Cheney:

    One of the concerns people have is that Israel might do it without being asked. …Given the fact that Iran has a stated policy that their objective is the destruction of Israel, the Israelis might well decide to act first, and let the rest of the world worry about cleaning up the diplomatic mess afterwards.9

    Commenting the Vice President’s assertion, former National Security adviser Zbigniew Brzezinski in an interview on PBS, confirmed with some apprehension, yes: Cheney wants Prime Minister Ariel Sharon to act on America’s behalf and “do it” for us:

    Iran I think is more ambiguous. And there the issue is certainly not tyranny; it’s nuclear weapons. And the vice president today in a kind of a strange parallel statement to this declaration of freedom hinted that the Israelis may do it and in fact used language which sounds like a justification or even an encouragement for the Israelis to do it.10

    What we are dealing with is a process of joint U.S.-NATO-Israel military planning. An operation to bomb Iran has been in the active planning stage since 2004. Officials in the Defense Department, under Bush and Obama, have been working assiduously with their Israeli military and intelligence counterparts, carefully identifying targets inside Iran. In practical military terms, any action by Israel would have to be planned and coordinated at the highest levels of the U.S. led coalition.

    Israel's Prime Minister Ariel Sharon and Vice President Dick Cheney discuss a vision of peace for Israel and Palestine as they conduct a press briefing in Jerusalem, Israel, March 19, 2002.

    Israel’s Prime Minister Ariel Sharon and Vice President Dick Cheney discuss a vision of peace for Israel and Palestine as they conduct a press briefing in Jerusalem, Israel, March 19, 2002. “It is our hope that the current violence and terrorism will be replaced by reconciliation and the rebuilding of mutual trust,” said the Vice President. (Source)

    An attack by Israel against Iran would also require coordinated U.S.-NATO logistical support, particularly with regard to Israel’s air defense system, which since January 2009 is fully integrated into that of the U.S. and NATO.11

    Israel’s X band radar system established in early 2009 with U.S. technical support has “integrate[d] Israel’s missile defenses with the U.S. global missile [Space-based] detection network, which includes satellites, Aegis ships on the Mediterranean, Persian Gulf and Red Sea, and land-based Patriot radars and interceptors.”12

    What this means is that Washington ultimately calls the shots. The U.S. rather than Israel controls the air defense system:

    This is and will remain a U.S. radar system,’ Pentagon spokesman Geoff Morrell said.

    ‘So this is not something we are giving or selling to the Israelis and it is something that will likely require U.S. personnel on-site to operate.13

    The U.S. military oversees Israel’s Air Defense system, which is integrated into the Pentagon’s global system. In other words, Israel cannot launch a war against Iran without Washington’s consent. Hence the importance of the so-called “Green Light” legislation in the U.S. Congress sponsored by the Republican party under House Resolution 1553, which explicitly supported an Israeli attack on Iran:

    The measure, introduced by Texas Republican Louie Gohmert and 46 of his colleagues, endorses Israel’s use of “all means necessary” against Iran “including the use of military force.” … “We’ve got to get this done. We need to show our support for Israel. We need to quit playing games with this critical ally in such a difficult area”.14

    In practice, the proposed legislation serves as a “Green Light” to the White House and the Pentagon rather than to Israel. It constitutes a rubber stamp to a U.S. sponsored war on Iran which uses Israel as a convenient military launch pad. It also serves as a justification to wage war with a view to defending Israel.

    In this context, Israel could indeed provide the pretext to wage war, in response to alleged Hamas or Hezbollah attacks and/or the triggering of hostilities on the border of Israel with Lebanon. What is crucial to understand is that a minor “incident” could be used as a pretext to spark off a major military operation against Iran.

    Known to U.S. military planners, Israel (rather than the U.S.A) would be the first target of military retaliation by Iran. Broadly speaking, Israelis would be the victims of the machinations of both Washington and their own government. It is, in this regard, absolutely crucial that Israelis forcefully oppose any action by the Netanyahu government to attack Iran.

    Global Warfare: The Role of U.S. Strategic Command (U.S.STRATCOM)

    In January 2005, at the outset of the military deployment and build-up directed against Iran, U.S.STRATCOM was identified as “the lead Combatant Command for integration and synchronization of DoD-wide efforts in combating weapons of mass destruction.”15 What this means is that the coordination of a large scale attack on Iran, including the various scenarios of escalation in and beyond the broader Middle East Central Asian region would be coordinated by U.S.STRATCOM. (See Chapter I).

    Confirmed by military documents as well as official statements, both the U.S. and Israel contemplate the use of nuclear weapons directed against Iran. In 2006, U.S. Strategic Command (U.S.STRATCOM) announced it had achieved an operational capability for rapidly striking targets around the globe using nuclear or conventional weapons. This announcement was made after the conduct of military simulations pertaining to a U.S. led nuclear attack against a fictional country.16

    Continuity in Relation to the Bush-Cheney Era

    President Obama has largely endorsed the doctrine of pre-emptive use of nuclear weapons formulated by the previous administration. Under the 2010 Nuclear Posture Review, the Obama administration confirmed “that it is reserving the right to use nuclear weapons against Iran” for its non-compliance with U.S. demands regarding its alleged (nonexistent) nuclear weapons program.17 The Obama administration has also intimated that it would use nukes in the case of an Iranian response to an Israeli attack on Iran. Israel has also drawn up its own “secret plans” to bomb Iran with tactical nuclear weapons:

    Israeli military commanders believe conventional strikes may no longer be enough to annihilate increasingly well-defended enrichment facilities. Several have been built beneath at least 70ft of concrete and rock. However, the nuclear-tipped bunker-busters would be used only if a conventional attack was ruled out and if the United States declined to intervene, senior sources said.18

    Obama’s statements on the use of nuclear weapons against Iran and North Korea are consistent with post-9/11 U.S. nuclear weapons doctrine, which allows for the use of tactical nuclear weapons in the conventional war theater.

    Through a propaganda campaign which has enlisted the support of “authoritative” nuclear scientists, mini-nukes are upheld as an instrument of peace, namely a means to combating “Islamic terrorism” and instating Western style “democracy” in Iran. The low-yield nukes have been cleared for “battlefield use”. They are slated to be used against Iran and Syria in the next stage of America’s “War on Terrorism” alongside conventional weapons:

    Administration officials argue that low-yield nuclear weapons are needed as a credible deterrent against rogue states. [Iran, Syria, North Korea] Their logic is that existing nuclear weapons are too destructive to be used except in a full-scale nuclear war. Potential enemies realize this, thus they do not consider the threat of nuclear retaliation to be credible. However, low-yield nuclear weapons are less destructive, thus might conceivably be used. That would make them more effective as a deterrent.19

    The preferred nuclear weapon to be used against Iran are tactical nuclear weapons (Made in America), namely bunker buster bombs with nuclear warheads (for example, B61-11), with an explosive capacity between one third to six times a Hiroshima bomb.

    The B61-11 is the “nuclear version” of the “conventional” BLU 113. or Guided Bomb Unit GBU-28. It can be delivered in much same way as the conventional bunker buster bomb.20 While the U.S. does not contemplate the use of strategic thermonuclear weapons against Iran, Israel’s nuclear arsenal is largely composed of thermonuclear bombs which are deployed and could be used in a war with Iran. Under Israel’s Jericho III missile system with a range between 4,800 km to 6,500 km, all Iran would be within reach.

    Radioactive Fallout

    The issue of radioactive fallout and contamination, while casually dismissed by U.S.-NATO military analysts, would be devastating, potentially affecting a large area of the broader Middle East (including Israel) and Central Asian region.

    In an utterly twisted logic, nuclear weapons are presented as a means to building peace and preventing “collateral damage”. Iran’s nonexistent nuclear weapons are a threat to global security, whereas those of the U.S. and Israel are instruments of peace “harmless to the surrounding civilian population.”

    “The Mother of All Bombs” (MOAB) Slated to be Used against Iran?

    Of military significance within the U.S. conventional weapons arsenal is the 21,500-pound “monster weapon” nicknamed the “mother of all bombs” The GBU-43/B or Massive Ordnance Air Blast bomb (MOAB) was categorized “as the most powerful non-nuclear weapon ever designed” with the the largest yield in the U.S. conventional arsenal. The MOAB was tested in early March 2003 before being deployed to the Iraq war theater. According to U.S. military sources, the Joint Chiefs of Staff had advised the government of Saddam Hussein prior to launching the 2003 that the “mother of all bombs” was to be used against Iraq. (There were unconfirmed reports that it had been used in Iraq).

    The U.S. Department of Defense already confirmed in 2009 that it intends to use the “Mother of All Bombs” (MOAB) against Iran. The MOAB is said to be ”ideally suited to hit deeply buried nuclear facilities such as Natanz or Qom in Iran”21. The truth of the matter is that the MOAB, given its explosive capacity, would result in significant civilian casualties. It is a conventional “killing machine” with a nuclear type mushroom cloud.



    The procurement of four MOABs was commissioned in October 2009 at the hefty cost of $58.4 million, ($14.6 million for each bomb). This amount includes the costs of development and testing as well as integration of the MOAB bombs onto B-2 stealth bombers. This procurement is directly linked to war preparations in relation to Iran. The notification was contained in a ninety-three-page “reprograming memo” which included the following instructions:

    “The Department has an Urgent Operational Need (UON) for the capability to strike hard and deeply buried targets in high threat environments. The MOAB [Mother of All Bombs] is the weapon of choice to meet the requirements of the UON [Urgent Operational Need].” It further states that the request is endorsed by Pacific Command (which has responsibility over North Korea) and Central Command (which has responsibility over Iran).23

    The Pentagon is planning on a process of extensive destruction of Iran’s infrastructure and mass civilian casualties through the combined use of tactical nukes and monster conventional mushroom cloud bombs, including the MOAB and the larger GBU-57A/B or Massive Ordnance Penetrator (MOP), which surpasses the MOAB in terms of explosive capacity.

    The MOP is described as “a powerful new bomb aimed squarely at the underground nuclear facilities of Iran and North Korea. The gargantuan bomb–longer than eleven persons standing shoulder-to-shoulder or more than twenty feet base to nose”.24

    These are WMDs in the true sense of the word. The not so hidden objective of the MOAB and MOP, including the American nickname used to casually describe the MOAB (“Mother of all Bombs”), is “mass destruction” and mass civilian casualties with a view to instilling fear and despair.

    State of the Art Weaponry: “War Made Possible Through New Technologies”

    The process of U.S. military decision making in relation to Iran is supported by Star Wars, the militarization of outer space and the revolution in communications and information systems. Given the advances in military technology and the development of new weapons systems, an attack on Iran could be significantly different in terms of the mix of weapons systems, when compared to the March 2003 Blitzkrieg launched against Iraq. The Iran operation is slated to use the most advanced weapons systems in support of its aerial attacks. In all likelihood, new weapons systems will be tested.

    The 2000 Project for the New American Century (PNAC) document entitled Rebuilding American Defenses, outlined the mandate of the U.S. military in terms of large scale theater wars, to be waged simultaneously in different regions of the World: “Fight and decisively win multiple, simultaneous major theater wars”. (See Chapter I)



    This formulation is tantamount to a global war of conquest by a single imperial superpower.

    The PNAC document also called for the transformation of U.S. forces to exploit the “revolution in military affairs”, namely the implementation of “war made possible through new technologies”.25 The latter consists in developing and perfecting a state of the art global killing machine based on an arsenal of sophisticated new weaponry, which would eventually replace the existing paradigms.

    Thus, it can be foreseen that the process of transformation will in fact be a two-stage process: first of transition, then of more thoroughgoing transformation. The breakpoint will come when a preponderance of new weapons systems begins to enter service, perhaps when, for example, unmanned aerial vehicles begin to be as numerous as manned aircraft. In this regard, the Pentagon should be very wary of making large investments in new programs –tanks, planes, aircraft carriers, for example– that would commit U.S. forces to current paradigms of warfare for many decades to come.26

    The war on Iran could indeed mark this crucial break-point, with new space-based weapons systems being applied with a view to disabling an enemy which has significant conventional military capabilities including more than half a million ground forces.

    Electromagnetic Weapons

    Electromagnetic weapons could be used to destabilize Iran’s communications systems, disable electric power generation, undermine and destabilize command and control, government infrastructure, transportation, energy, etc. Within the same family of weapons, environmental modifications techniques (ENMOD) (weather warfare) developed under the HAARP program could also be applied.27 These weapons systems are fully operational. In this context, the U.S. Air Force document AF 2025 explicitly acknowledged the military applications of weather modification technologies:

    Weather modification will become a part of domestic and international security and could be done unilaterally. … It could have offensive and defensive applications and even be used for deterrence purposes. The ability to generate precipitation, fog, and storms on earth or to modify space weather, improve communications through ionospheric modification (the use of ionospheric mirrors), and the production of artificial weather all are a part of an integrated set of technologies which can provide substantial increase in U.S., or degraded capability in an adversary, to achieve global awareness, reach, and power.28

    Electromagnetic radiation enabling “remote health impairment” might also be envisaged in the war theater.29 In turn, new uses of biological weapons by the U.S. military might also be envisaged as suggested by the PNAC: “[A]dvanced forms of biological warfare that can ‘target’ specific genotypes may transform biological warfare from the realm of terror to a politically useful tool.”30

    Iran’s Military Capabilities: Medium and Long-range Missiles

    Iran has advanced military capabilities, including medium and long-range missiles capable of reaching targets in Israel and the Gulf States. Hence the emphasis by the U.S.-NATO Israel alliance on the use of nuclear weapons, which are slated to be used either pre-emptively or in response to an Iranian retaliatory missile attack.

    In November 2006, Iran tests of surface missiles two were marked by precise planning in a carefully staged operation. According to a senior American missile expert, “the Iranians demonstrated up-to-date missile-launching technology which the West had not known them to possess.”31 Israel acknowledged that “the Shehab-3, whose 2,000-km range brings Israel, the Middle East and Europe within reach”.32

    According to Uzi Rubin, former head of Israel’s anti-ballistic missile program, “the intensity of the military exercise was unprecedented… It was meant to make an impression – and it made an impression.”33

    The 2006 exercises, while creating a political stir in the U.S. and Israel, did not in any way modify U.S.-NATO-Israeli resolve to wage war on Iran.

    Tehran has confirmed in several statements that it will respond if it is attacked. Israel would be the immediate object of Iranian missile attacks as confirmed by the Iranian government. The issue of Israel’s air defense system is therefore crucial. U.S. and allied military facilities in the Gulf states, Turkey, Saudi Arabia, Afghanistan and Iraq could also be targeted by Iran.

    Iran’s Ground Forces

    While Iran is encircled by U.S. and allied military bases, the Islamic Republic has significant military capabilities. What is important to acknowledge is the sheer size of Iranian forces in terms of personnel (army, navy, air force) when compared to U.S. and NATO forces serving in Afghanistan and Iraq.

    Confronted with a well-organized insurgency, coalition forces are already overstretched in both Afghanistan and Iraq. Would these forces be able to cope if Iranian ground forces were to enter the existing battlefield in Iraq and Afghanistan? The potential of the Resistance movement to U.S. and allied occupation would inevitably be affected.

    Iranian ground forces are of the order of 700,000 of which 130,000 are professional soldiers, 220,000 are conscripts and 350,000 are reservists.34 There are 18,000 personnel in Iran’s Navy and 52,000 in the Air Force. According to the International Institute for Strategic Studies, “the Revolutionary Guards has an estimated 125,000 personnel in five branches: Its own Navy, Air Force, and Ground Forces; and the Quds Force (Special Forces).”

    According to the CISS, Iran’s Basij paramilitary volunteer force controlled by the Revolu- tionary Guards “has an estimated 90,000 active-duty full-time uniformed members, 300,000 reservists, and a total of 11 million men that can be mobilized if need be”35, In other words, Iran can mobilize up to half a million regular troops and several million militia. Its Quds special forces are already operating inside Iraq.

    U.S. Military and Allied Facilities Surrounding Iran

    For several years now, Iran has been conducting its own war drills and exercises. While its Air Force has weaknesses, its intermediate and long-range missiles are fully operational. Iran’s military is in a state of readiness. Iranian troop concentrations are currently within a few kilometers of the Iraqi and Afghan borders, and within proximity of Kuwait. The Iranian Navy is deployed in the Persian Gulf within proximity of U.S. and allied military facilities in the United Arab Emirates.

    It is worth noting that in response to Iran’s military build-up, the U.S. has been transferring large amounts of weapons to its non-NATO allies in the Persian Gulf including Kuwait and Saudi Arabia.

    While Iran’s advanced weapons do not measure up to those of the U.S. and NATO, Iranian forces would be in a position to inflict substantial losses to coalition forces in a conventional war theater, on the ground in Iraq or Afghanistan. Iranian ground troops and tanks in December 2009 crossed the border into Iraq without being confronted or challenged by allied forces and occupied a disputed territory in the East Maysan oil field.

    Even in the event of an effective Blitzkrieg, which targets Iran’s military facilities, its communications systems etc., through massive aerial bombing, using cruise missiles, conventional bunker buster bombs and tactical nuclear weapons, a war with Iran, once initiated, could eventually lead into a ground war. This is something which U.S. military planners have no doubt contemplated in their simulated war scenarios.

    An operation of this nature would result in significant military and civilian casualties, particularly if nuclear weapons are used.

    Within a scenario of escalation, Iranian troops could cross the border into Iraq and Afghanistan.

    In turn, military escalation using nuclear weapons could lead us into a World War III scenario, extending beyond the Middle-East – Central Asian region.

    In a very real sense, this military project, which has been on the Pentagon’s drawing board for more than ten years, threatens the future of humanity.

    Our focus in this chapter has been on war preparations. The fact that war preparations are in an advanced state of readiness does not imply that these war plans will be carried out.

    The U.S.-NATO-Israel alliance realizes that the enemy has significant capabilities to respond and retaliate. This factor in itself has been crucial in the decision by the U.S. and its allies to postpone an attack on Iran.

    Another crucial factor is the structure of military alliances. Whereas NATO has become a formidable force, the Shanghai Cooperation Organization (SCO), which constitutes an alliance between Russia and China and a number of former Soviet Republics has been significantly weakened.

    The ongoing U.S. military threats directed against China and Russia are intended to weaken the SCO and discourage any form of military action on the part of Iran’s allies in the case of a U.S. NATO Israeli attack.

    Video Interview: Michel Chossudovsky and Caroline Mailloux

    November 2023 Interview

    Notes

    1. See Target Iran – Air Strikes, Globalsecurity.org, undated.

    2. William Arkin, Washington Post, April 16, 2006.

    3. Ibid.

    4. New Statesman, February 19, 2007.

    5. Philip Giraldi, Deep Background,The American Conservative August 2005.

    6. U.S.CENTCOM, http://www.milnet.com/milnet/pentagon/centcom/chap1/stratgic.htm#U.S.Policy, link no longer active,

    archived at http://tinyurl.com/37gafu9.

    7. General Wesley Clark, for further details see Chapter I.

    8. See Michel Chossudovsky, Planned U.S.-Israeli Attack on Iran, Global Research, May 1, 2005.

    9. Dick Cheney, quoted from an MSNBC Interview, January 2005.

    10. According to Zbigniew Brzezinski.

    11. Michel Chossudovsky, Unusually Large U.S. Weapons Shipment to Israel: Are the U.S. and Israel Planning a Broader Middle East War? Global Research, January 11, 2009.

    12. Defense Talk.com, January 6, 2009.

    13. Quoted in Israel National News, January 9, 2009.

    14. Webster Tarpley, Fidel Castro Warns of Imminent Nuclear War; Admiral Mullen Threatens Iran; U.S.-Israel versus Iran-Hezbollah Confrontation Builds On, Global Research, August 10, 2010.

    15. Michel Chossudovsky, Nuclear War against Iran, Global Research, January 3, 2006.

    16. David Ruppe, Pre-emptive Nuclear War in a State of Readiness: U.S. Command Declares Global Strike Ca- pability, Global Security Newswire, December 2, 2005.

    17. U.S. Nuclear Option on Iran Linked to Israeli Attack Threat – IPS ipsnews.net, April 23, 2010.

    18. Revealed: Israel plans nuclear strike on Iran – Times Online, January 7, 2007.

    19. Opponents Surprised By Elimination of Nuke Research Funds, Defense News, November 29, 2004.

    20. See Michel Chossudovsky, “Tactical Nuclear Weapons” against Afghanistan?, Global Research, December 5, 2001. See also http://www.thebulletin.org/article_nn.php?art_ofn=jf03norris.

    21. Jonathan Karl, Is the U.S. Preparing to Bomb Iran? ABC News, October 9, 2009.

    22. Ibid.

    23. ABC News, op cit, emphasis added. To consult the reprogramming request (pdf) click here.

    24. See Edwin Black, “Super Bunker-Buster Bombs Fast-Tracked for Possible Use Against Iran and North Korea Nuclear Programs”, Cutting Edge, September 21, 2009.

    25. See Project for a New American Century, Rebuilding America’s Defenses Washington DC, September 2000, pdf.

    26. Ibid, emphasis added.

    27. See Michel Chossudovsky, “Owning the Weather” for Military Use, Global Research, September 27, 2004. 28. Air
    Force 2025 Final Report, See also U.S. Air Force: Weather as a Force Multiplier: Owning the Weather in 2025, AF2025
    v3c15-1.

    29. See Mojmir Babacek, Electromagnetic and Informational Weapons:, Global Research, August 6, 2004.

    30. Project for a New American Century, op cit., p. 60.

    31. See Michel Chossudovsky, Iran’s “Power of Deterrence” Global Research, November 5, 2006.

    32. Debka, November 5, 2006.

    33. www.cnsnews.com November 3, 2006.

    34. See Islamic Republic of Iran Army – Wikipedia.

    Featured image is from The Libertarian Institute

    The Globalization of War: America’s “Long War” against Humanity

    Michel Chossudovsky

    The “globalization of war” is a hegemonic project. Major military and covert intelligence operations are being undertaken simultaneously in the Middle East, Eastern Europe, sub-Saharan Africa, Central Asia and the Far East. The U.S. military agenda combines both major theater operations as well as covert actions geared towards destabilizing sovereign states.

    ISBN Number: 978-0-9879389-0-9

    Year: 2015
    Pages: 240 Pages
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    Pre-emptive Nuclear War: The Role of Israel in Triggering an Attack on Iran Chapter III of "The Globalization of War" by Michel Chossudovsky Firmly All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name. To receive Global Research’s Daily Newsletter (selected articles), click here. Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. Author’s Introduction and Update In a recent article entitled “A Planned US-Israeli Attack on Iran is Contemplated” I focussed on how Israel’s criminal attack on the People of Palestine could evolve towards an extended Middle East War. At the time of writing, US-NATO war ships –including two aircraft carriers, combat planes, not to mention a nuclear submarine– are deployed in the Eastern Mediterranean and the Red Sea, all of which are intended to confront what both Western politicians and the media casually describe as “Palestine’s Aggression against the Jewish State”. “Israel ranks” as “the 4th strongest military” after Russia, the U.S and China. Ask yourself: Why on earth would Israel need the support of U.S. aircraft carriers to lead a genocide against the Palestinians who are fighting for their lives with limited military capabilities. Is the U.S. intent upon triggering a broader war? “U.S. Warns Hezbollah, Iran. It Will intervene if they Escalate” Who is “Escalating”? The Pentagon has already intimated that it will attack Iran and Lebanon, “If they Escalate”. Is the Pentagon Seeking to Trigger one or more “False Flags”? Times of Israel, November 9, 2023 Also of significance (less than 4 months prior to October 7, 2023) is the adoption on June 27, 2023 of the US Congress Resolution (H. RES. 559) which Accuses Iran of Possessing Nuclear Weapons. H.RES 559 allows the use of force against Iran, intimating that Iran has Nuclear Weapons. Whereas Iran is tagged (without a shred of evidence) as a Nuclear Power by the U.S. Congress, Washington fails to acknowledge that Israel is an undeclared nuclear power. The article below was first published in my book entitled “The Globalization of War. America’s Long War against Humanity” (2015). I remain indebted to the former Prime Minister of Malaysia Tun Dr. Mahathir Mohamad who took the initiative of launching my book in Kuala Lumpur. (image right). Firmly committed to “the criminalization of war”, Tun Mahathir is a powerful voice in support of Palestine. The article below (Chapter III of “Globalization of War”) provides analysis in a historical perspective of U.S. war plans directed against Iran. Numerous “war theater scenarios” for an all-out attack on Iran have been contemplated. Dangerous Crossroads in our History The current and ongoing US-NATO military deployment in The Middle East — casually presented by the media as a means to coming to the rescue of Israel– is the pinnacle of U.S. war preparations extending over a period of more than 20 years. Contemplated by the Pentagon in 2005 was a scenario whereby an attack by Israel would be conducted on behalf of Washington: “An attack by Israel could, however, be used as “the trigger mechanism” which would unleash an all-out war against Iran, as well as retaliation by Iran directed against Israel.” (quoted from text below) At the outset of Bush’s second term “Vice President Dick Cheney had hinted, in no uncertain terms, that Iran was “right at the top of the list” of the “rogue enemies” of America, and that Israel would, so to speak, “be doing the bombing for us” (Ibid) The article also focusses on the dangers of a US-Israel nuclear attack against Iran which has been contemplated by the Pentagon since 2004. The US Israel “Partnership”: “Signed” Military Agreement Amply documented, the U.S. Military and Intelligence apparatus is firmly behind Israel’s genocide. In the words of Lt General Richard Clark: Americans Troops are “prepared to die for the Jewish State”. What should be understood by this statement is that the US and Israel have a longstanding Military “Partnership” as well as (Jerusalem Post) a “Signed” Military Agreement (classified) regarding Israel’s attack on Gaza. Lt. General Richard Clark is U.S. Third Air Force Commander, among the highest-ranking military officers in the U.S. Armed Forces. While he refers to Juniper Cobra, “a joint military exercise that has been conducted for almost a decade”, his statement points to a much broader “signed” military-intelligence agreement (classified) with Israel which no doubt includes the extension of the Israeli-US bombing of Gaza to the broader Middle East. While this so-called “signed” military agreement remains classified (not in the public domain), it would appear that Biden is obeying the orders of the perpetrators of this diabolical military agenda. Does President Biden have the authority (under this “Signed” Agreement with Israel) to save the lives of innocent civilians including the children of Palestine: Q (Inaudible) Gaza ceasefire, Mr. President? THE PRESIDENT: Pardon me? Q What are the chances of a Gaza ceasefire? THE PRESIDENT: None. No possibility. White House Press Conference, November 9, 2023 Lt. General Clark confirms that: “U.S. troops could be put under Israeli commanders in the battlefield”, which suggests that the genocide is implemented by Netanyahu on behalf of the United States. Everything indicates that the US military and intelligence apparatus are behind Israel’s criminal bombing and invasion of Gaza. We stand firmly in Solidarity with Palestine and the People of the Middle East. It is my intent and sincere hope that my writings (including the text below) will contribute to “Revealing the Truth” as well “Reversing the Tide of Global Warfare”. Michel Chossudovsky, Global Research, November 17, 2023, March 10, 2024 Pre-emptive Nuclear War: The Role of Israel in Triggering an Attack on Iran by Michel Chossudovsky Introduction While one can conceptualize the loss of life and destruction resulting from present-day wars including Iraq and Afghanistan, it is impossible to fully comprehend the devastation which might result from a Third World War, using “new technologies” and advanced weapons, until it occurs and becomes a reality. The international community has endorsed nuclear war in the name of world peace. “Making the world safer” is the justification for launching a military operation which could potentially result in a nuclear holocaust.” The stockpiling and deployment of advanced weapons systems directed against Iran started in the immediate wake of the 2003 bombing and invasion of Iraq. From the outset, these war plans were led by the U.S. in liaison with NATO and Israel. Following the 2003 invasion of Iraq, the Bush administration identified Iran and Syria as the next stage of “the road map to war”. U.S. military sources intimated at the time that an aerial attack on Iran could involve a large scale deployment comparable to the U.S. “shock and awe” bombing raids on Iraq in March 2003: American air strikes on Iran would vastly exceed the scope of the 1981 Israeli attack on the Osiraq nuclear center in Iraq, and would more resemble the opening days of the 2003 air campaign against Iraq.1 “Theater Iran Near Term” (TIRANNT) Code named by U.S. military planners as TIRANNT, “Theater Iran Near Term”, simulations of an attack on Iran were initiated in May 2003 “when modelers and intelligence specialists pulled together the data needed for theater-level (meaning large-scale) scenario analysis for Iran.”2 The scenarios identified several thousand targets inside Iran as part of a “Shock and Awe” Blitzkrieg: The analysis, called TIRANNT, for “Theater Iran Near Term,” was coupled with a mock scenario for a Marine Corps invasion and a simulation of the Iranian missile force. U.S. and British planners conducted a Caspian Sea war game around the same time. And Bush directed the U.S. Strategic Command to draw up a global strike war plan for an attack against Iranian weapons of mass destruction. All of this will ultimately feed into a new war plan for “major combat operations” against Iran that military sources confirm now [April 2006] exists in draft form. … Under TIRANNT, Army and U.S. Central Command planners have been examining both near-term and out-year scenarios for war with Iran, including all aspects of a major combat operation, from mobilization and deployment of forces through postwar stability operations after regime change.3 Different “theater scenarios” for an all-out attack on Iran had been contemplated: The U.S. army, navy, air force and marines have all prepared battle plans and spent four years building bases and training for “Operation Iranian Freedom”. Admiral Fallon, the new head of U.S. Central Command, has inherited computerized plans under the name TIRANNT (Theatre Iran Near Term).4 In 2004, drawing upon the initial war scenarios under TIRANNT, Vice President Dick Cheney instructed U.S. Strategic Command (U.S.STRATCOM) to draw up a “contingency plan” of a large scale military operation directed against Iran “to be employed in response to another 9/11-type terrorist attack on the United States” on the presumption that the government in Tehran would be behind the terrorist plot. The plan included the pre-emptive use of nuclear weapons against a non-nuclear state: The plan includes a large-scale air assault on Iran employing both conventional and tactical nuclear weapons. Within Iran there are more than four hundred fifty major strategic targets, including numerous suspected nuclear-weapons-program develop- ment sites. Many of the targets are hardened or are deep underground and could not be taken out by conventional weapons, hence the nuclear option. As in the case of Iraq, the response is not conditional on Iran actually being involved in the act of ter- rorism directed against the United States. Several senior Air Force officers involved in the planning are reportedly appalled at the implications of what they are doing –that Iran is being set up for an unprovoked nuclear attack– but no one is prepared to dam- age his career by posing any objections.5 The Military Road Map: “First Iraq, then Iran” The decision to target Iran under TIRANNT was part of the broader process of military planning and sequencing of military operations. Already under the Clinton administration (1995), U.S. Central Command (U.S.CENTCOM) had formulated “in war theater plans” to invade first Iraq and then Iran. Access to Middle East oil was the stated strategic objective: The broad national security interests and objectives expressed in the President’s National Security Strategy (NSS) and the Chairman’s National Military Strategy (NMS) form the foundation of the United States Central Command’s theater strategy. The NSS directs implementation of a strategy of dual containment of the rogue states of Iraq and Iran as long as those states pose a threat to U.S. interests, to other states in the region, and to their own citizens. Dual containment is designed to maintain the balance of power in the region without depending on either Iraq or Iran. U.S.CENTCOM’s theater strategy is interest-based and threat-focused. The purpose of U.S. engagement, as espoused in the NSS, is to protect the United States’ vital interest in the region – uninterrupted, secure U.S./Allied access to Gulf oil.6 The war on Iran was viewed as part of a succession of military operations. According to (former) NATO Commander General Wesley Clark, the Pentagon’s military road-map consisted of a sequence of countries: [The] Five-year campaign plan [includes]… a total of seven countries, beginning with Iraq, then Syria, Lebanon, Libya, Iran, Somalia and Sudan.6 (For further details, see Chapter I) The Role of Israel There has been much debate regarding the role of Israel in initiating an attack against Iran. Israel is part of a military alliance. Tel Aviv is not a prime mover. It does not have a separate and distinct military agenda. Israel is integrated into the “war plan for major combat operations” against Iran formulated in 2006 by U.S. Strategic Command (U.S.STRATCOM). In the context of large scale military operations, an uncoordinated unilateral military action by one coalition partner, namely Israel, is from a military and strategic point almost an impossibility. Israel is a de facto member of NATO. Any action by Israel would require a “green light” from Washington. An attack by Israel could, however, be used as “the trigger mechanism” which would unleash an all-out war against Iran, as well as retaliation by Iran directed against Israel. In this regard, there are indications going back to the Bush administration that Washington had indeed contemplated the option of an initial (U.S. backed) attack by Israel rather than an outright U.S.-led military operation directed against Iran. The Israeli attack –although led in close liaison with the Pentagon and NATO– would have been presented to public opinion as a unilateral decision by Tel Aviv. It would then have been used by Washington to justify, in the eyes of World opinion, a military intervention of the U.S. and NATO with a view to “defending Israel”, rather than attacking Iran. Under existing military cooperation agreements, both the U.S. and NATO would be “obligated” to “defend Israel” against Iran and Syria. It is worth noting, in this regard, that at the outset of Bush’s second term, (former) Vice President Dick Cheney had hinted, in no uncertain terms, that Iran was “right at the top of the list” of the “rogue enemies” of America, and that Israel would, so to speak, “be doing the bombing for us”, without U.S. military involvement and without us putting pressure on them “to do it.”8 According to Cheney: One of the concerns people have is that Israel might do it without being asked. …Given the fact that Iran has a stated policy that their objective is the destruction of Israel, the Israelis might well decide to act first, and let the rest of the world worry about cleaning up the diplomatic mess afterwards.9 Commenting the Vice President’s assertion, former National Security adviser Zbigniew Brzezinski in an interview on PBS, confirmed with some apprehension, yes: Cheney wants Prime Minister Ariel Sharon to act on America’s behalf and “do it” for us: Iran I think is more ambiguous. And there the issue is certainly not tyranny; it’s nuclear weapons. And the vice president today in a kind of a strange parallel statement to this declaration of freedom hinted that the Israelis may do it and in fact used language which sounds like a justification or even an encouragement for the Israelis to do it.10 What we are dealing with is a process of joint U.S.-NATO-Israel military planning. An operation to bomb Iran has been in the active planning stage since 2004. Officials in the Defense Department, under Bush and Obama, have been working assiduously with their Israeli military and intelligence counterparts, carefully identifying targets inside Iran. In practical military terms, any action by Israel would have to be planned and coordinated at the highest levels of the U.S. led coalition. Israel's Prime Minister Ariel Sharon and Vice President Dick Cheney discuss a vision of peace for Israel and Palestine as they conduct a press briefing in Jerusalem, Israel, March 19, 2002. Israel’s Prime Minister Ariel Sharon and Vice President Dick Cheney discuss a vision of peace for Israel and Palestine as they conduct a press briefing in Jerusalem, Israel, March 19, 2002. “It is our hope that the current violence and terrorism will be replaced by reconciliation and the rebuilding of mutual trust,” said the Vice President. (Source) An attack by Israel against Iran would also require coordinated U.S.-NATO logistical support, particularly with regard to Israel’s air defense system, which since January 2009 is fully integrated into that of the U.S. and NATO.11 Israel’s X band radar system established in early 2009 with U.S. technical support has “integrate[d] Israel’s missile defenses with the U.S. global missile [Space-based] detection network, which includes satellites, Aegis ships on the Mediterranean, Persian Gulf and Red Sea, and land-based Patriot radars and interceptors.”12 What this means is that Washington ultimately calls the shots. The U.S. rather than Israel controls the air defense system: This is and will remain a U.S. radar system,’ Pentagon spokesman Geoff Morrell said. ‘So this is not something we are giving or selling to the Israelis and it is something that will likely require U.S. personnel on-site to operate.13 The U.S. military oversees Israel’s Air Defense system, which is integrated into the Pentagon’s global system. In other words, Israel cannot launch a war against Iran without Washington’s consent. Hence the importance of the so-called “Green Light” legislation in the U.S. Congress sponsored by the Republican party under House Resolution 1553, which explicitly supported an Israeli attack on Iran: The measure, introduced by Texas Republican Louie Gohmert and 46 of his colleagues, endorses Israel’s use of “all means necessary” against Iran “including the use of military force.” … “We’ve got to get this done. We need to show our support for Israel. We need to quit playing games with this critical ally in such a difficult area”.14 In practice, the proposed legislation serves as a “Green Light” to the White House and the Pentagon rather than to Israel. It constitutes a rubber stamp to a U.S. sponsored war on Iran which uses Israel as a convenient military launch pad. It also serves as a justification to wage war with a view to defending Israel. In this context, Israel could indeed provide the pretext to wage war, in response to alleged Hamas or Hezbollah attacks and/or the triggering of hostilities on the border of Israel with Lebanon. What is crucial to understand is that a minor “incident” could be used as a pretext to spark off a major military operation against Iran. Known to U.S. military planners, Israel (rather than the U.S.A) would be the first target of military retaliation by Iran. Broadly speaking, Israelis would be the victims of the machinations of both Washington and their own government. It is, in this regard, absolutely crucial that Israelis forcefully oppose any action by the Netanyahu government to attack Iran. Global Warfare: The Role of U.S. Strategic Command (U.S.STRATCOM) In January 2005, at the outset of the military deployment and build-up directed against Iran, U.S.STRATCOM was identified as “the lead Combatant Command for integration and synchronization of DoD-wide efforts in combating weapons of mass destruction.”15 What this means is that the coordination of a large scale attack on Iran, including the various scenarios of escalation in and beyond the broader Middle East Central Asian region would be coordinated by U.S.STRATCOM. (See Chapter I). Confirmed by military documents as well as official statements, both the U.S. and Israel contemplate the use of nuclear weapons directed against Iran. In 2006, U.S. Strategic Command (U.S.STRATCOM) announced it had achieved an operational capability for rapidly striking targets around the globe using nuclear or conventional weapons. This announcement was made after the conduct of military simulations pertaining to a U.S. led nuclear attack against a fictional country.16 Continuity in Relation to the Bush-Cheney Era President Obama has largely endorsed the doctrine of pre-emptive use of nuclear weapons formulated by the previous administration. Under the 2010 Nuclear Posture Review, the Obama administration confirmed “that it is reserving the right to use nuclear weapons against Iran” for its non-compliance with U.S. demands regarding its alleged (nonexistent) nuclear weapons program.17 The Obama administration has also intimated that it would use nukes in the case of an Iranian response to an Israeli attack on Iran. Israel has also drawn up its own “secret plans” to bomb Iran with tactical nuclear weapons: Israeli military commanders believe conventional strikes may no longer be enough to annihilate increasingly well-defended enrichment facilities. Several have been built beneath at least 70ft of concrete and rock. However, the nuclear-tipped bunker-busters would be used only if a conventional attack was ruled out and if the United States declined to intervene, senior sources said.18 Obama’s statements on the use of nuclear weapons against Iran and North Korea are consistent with post-9/11 U.S. nuclear weapons doctrine, which allows for the use of tactical nuclear weapons in the conventional war theater. Through a propaganda campaign which has enlisted the support of “authoritative” nuclear scientists, mini-nukes are upheld as an instrument of peace, namely a means to combating “Islamic terrorism” and instating Western style “democracy” in Iran. The low-yield nukes have been cleared for “battlefield use”. They are slated to be used against Iran and Syria in the next stage of America’s “War on Terrorism” alongside conventional weapons: Administration officials argue that low-yield nuclear weapons are needed as a credible deterrent against rogue states. [Iran, Syria, North Korea] Their logic is that existing nuclear weapons are too destructive to be used except in a full-scale nuclear war. Potential enemies realize this, thus they do not consider the threat of nuclear retaliation to be credible. However, low-yield nuclear weapons are less destructive, thus might conceivably be used. That would make them more effective as a deterrent.19 The preferred nuclear weapon to be used against Iran are tactical nuclear weapons (Made in America), namely bunker buster bombs with nuclear warheads (for example, B61-11), with an explosive capacity between one third to six times a Hiroshima bomb. The B61-11 is the “nuclear version” of the “conventional” BLU 113. or Guided Bomb Unit GBU-28. It can be delivered in much same way as the conventional bunker buster bomb.20 While the U.S. does not contemplate the use of strategic thermonuclear weapons against Iran, Israel’s nuclear arsenal is largely composed of thermonuclear bombs which are deployed and could be used in a war with Iran. Under Israel’s Jericho III missile system with a range between 4,800 km to 6,500 km, all Iran would be within reach. Radioactive Fallout The issue of radioactive fallout and contamination, while casually dismissed by U.S.-NATO military analysts, would be devastating, potentially affecting a large area of the broader Middle East (including Israel) and Central Asian region. In an utterly twisted logic, nuclear weapons are presented as a means to building peace and preventing “collateral damage”. Iran’s nonexistent nuclear weapons are a threat to global security, whereas those of the U.S. and Israel are instruments of peace “harmless to the surrounding civilian population.” “The Mother of All Bombs” (MOAB) Slated to be Used against Iran? Of military significance within the U.S. conventional weapons arsenal is the 21,500-pound “monster weapon” nicknamed the “mother of all bombs” The GBU-43/B or Massive Ordnance Air Blast bomb (MOAB) was categorized “as the most powerful non-nuclear weapon ever designed” with the the largest yield in the U.S. conventional arsenal. The MOAB was tested in early March 2003 before being deployed to the Iraq war theater. According to U.S. military sources, the Joint Chiefs of Staff had advised the government of Saddam Hussein prior to launching the 2003 that the “mother of all bombs” was to be used against Iraq. (There were unconfirmed reports that it had been used in Iraq). The U.S. Department of Defense already confirmed in 2009 that it intends to use the “Mother of All Bombs” (MOAB) against Iran. The MOAB is said to be ”ideally suited to hit deeply buried nuclear facilities such as Natanz or Qom in Iran”21. The truth of the matter is that the MOAB, given its explosive capacity, would result in significant civilian casualties. It is a conventional “killing machine” with a nuclear type mushroom cloud. The procurement of four MOABs was commissioned in October 2009 at the hefty cost of $58.4 million, ($14.6 million for each bomb). This amount includes the costs of development and testing as well as integration of the MOAB bombs onto B-2 stealth bombers. This procurement is directly linked to war preparations in relation to Iran. The notification was contained in a ninety-three-page “reprograming memo” which included the following instructions: “The Department has an Urgent Operational Need (UON) for the capability to strike hard and deeply buried targets in high threat environments. The MOAB [Mother of All Bombs] is the weapon of choice to meet the requirements of the UON [Urgent Operational Need].” It further states that the request is endorsed by Pacific Command (which has responsibility over North Korea) and Central Command (which has responsibility over Iran).23 The Pentagon is planning on a process of extensive destruction of Iran’s infrastructure and mass civilian casualties through the combined use of tactical nukes and monster conventional mushroom cloud bombs, including the MOAB and the larger GBU-57A/B or Massive Ordnance Penetrator (MOP), which surpasses the MOAB in terms of explosive capacity. The MOP is described as “a powerful new bomb aimed squarely at the underground nuclear facilities of Iran and North Korea. The gargantuan bomb–longer than eleven persons standing shoulder-to-shoulder or more than twenty feet base to nose”.24 These are WMDs in the true sense of the word. The not so hidden objective of the MOAB and MOP, including the American nickname used to casually describe the MOAB (“Mother of all Bombs”), is “mass destruction” and mass civilian casualties with a view to instilling fear and despair. State of the Art Weaponry: “War Made Possible Through New Technologies” The process of U.S. military decision making in relation to Iran is supported by Star Wars, the militarization of outer space and the revolution in communications and information systems. Given the advances in military technology and the development of new weapons systems, an attack on Iran could be significantly different in terms of the mix of weapons systems, when compared to the March 2003 Blitzkrieg launched against Iraq. The Iran operation is slated to use the most advanced weapons systems in support of its aerial attacks. In all likelihood, new weapons systems will be tested. The 2000 Project for the New American Century (PNAC) document entitled Rebuilding American Defenses, outlined the mandate of the U.S. military in terms of large scale theater wars, to be waged simultaneously in different regions of the World: “Fight and decisively win multiple, simultaneous major theater wars”. (See Chapter I) This formulation is tantamount to a global war of conquest by a single imperial superpower. The PNAC document also called for the transformation of U.S. forces to exploit the “revolution in military affairs”, namely the implementation of “war made possible through new technologies”.25 The latter consists in developing and perfecting a state of the art global killing machine based on an arsenal of sophisticated new weaponry, which would eventually replace the existing paradigms. Thus, it can be foreseen that the process of transformation will in fact be a two-stage process: first of transition, then of more thoroughgoing transformation. The breakpoint will come when a preponderance of new weapons systems begins to enter service, perhaps when, for example, unmanned aerial vehicles begin to be as numerous as manned aircraft. In this regard, the Pentagon should be very wary of making large investments in new programs –tanks, planes, aircraft carriers, for example– that would commit U.S. forces to current paradigms of warfare for many decades to come.26 The war on Iran could indeed mark this crucial break-point, with new space-based weapons systems being applied with a view to disabling an enemy which has significant conventional military capabilities including more than half a million ground forces. Electromagnetic Weapons Electromagnetic weapons could be used to destabilize Iran’s communications systems, disable electric power generation, undermine and destabilize command and control, government infrastructure, transportation, energy, etc. Within the same family of weapons, environmental modifications techniques (ENMOD) (weather warfare) developed under the HAARP program could also be applied.27 These weapons systems are fully operational. In this context, the U.S. Air Force document AF 2025 explicitly acknowledged the military applications of weather modification technologies: Weather modification will become a part of domestic and international security and could be done unilaterally. … It could have offensive and defensive applications and even be used for deterrence purposes. The ability to generate precipitation, fog, and storms on earth or to modify space weather, improve communications through ionospheric modification (the use of ionospheric mirrors), and the production of artificial weather all are a part of an integrated set of technologies which can provide substantial increase in U.S., or degraded capability in an adversary, to achieve global awareness, reach, and power.28 Electromagnetic radiation enabling “remote health impairment” might also be envisaged in the war theater.29 In turn, new uses of biological weapons by the U.S. military might also be envisaged as suggested by the PNAC: “[A]dvanced forms of biological warfare that can ‘target’ specific genotypes may transform biological warfare from the realm of terror to a politically useful tool.”30 Iran’s Military Capabilities: Medium and Long-range Missiles Iran has advanced military capabilities, including medium and long-range missiles capable of reaching targets in Israel and the Gulf States. Hence the emphasis by the U.S.-NATO Israel alliance on the use of nuclear weapons, which are slated to be used either pre-emptively or in response to an Iranian retaliatory missile attack. In November 2006, Iran tests of surface missiles two were marked by precise planning in a carefully staged operation. According to a senior American missile expert, “the Iranians demonstrated up-to-date missile-launching technology which the West had not known them to possess.”31 Israel acknowledged that “the Shehab-3, whose 2,000-km range brings Israel, the Middle East and Europe within reach”.32 According to Uzi Rubin, former head of Israel’s anti-ballistic missile program, “the intensity of the military exercise was unprecedented… It was meant to make an impression – and it made an impression.”33 The 2006 exercises, while creating a political stir in the U.S. and Israel, did not in any way modify U.S.-NATO-Israeli resolve to wage war on Iran. Tehran has confirmed in several statements that it will respond if it is attacked. Israel would be the immediate object of Iranian missile attacks as confirmed by the Iranian government. The issue of Israel’s air defense system is therefore crucial. U.S. and allied military facilities in the Gulf states, Turkey, Saudi Arabia, Afghanistan and Iraq could also be targeted by Iran. Iran’s Ground Forces While Iran is encircled by U.S. and allied military bases, the Islamic Republic has significant military capabilities. What is important to acknowledge is the sheer size of Iranian forces in terms of personnel (army, navy, air force) when compared to U.S. and NATO forces serving in Afghanistan and Iraq. Confronted with a well-organized insurgency, coalition forces are already overstretched in both Afghanistan and Iraq. Would these forces be able to cope if Iranian ground forces were to enter the existing battlefield in Iraq and Afghanistan? The potential of the Resistance movement to U.S. and allied occupation would inevitably be affected. Iranian ground forces are of the order of 700,000 of which 130,000 are professional soldiers, 220,000 are conscripts and 350,000 are reservists.34 There are 18,000 personnel in Iran’s Navy and 52,000 in the Air Force. According to the International Institute for Strategic Studies, “the Revolutionary Guards has an estimated 125,000 personnel in five branches: Its own Navy, Air Force, and Ground Forces; and the Quds Force (Special Forces).” According to the CISS, Iran’s Basij paramilitary volunteer force controlled by the Revolu- tionary Guards “has an estimated 90,000 active-duty full-time uniformed members, 300,000 reservists, and a total of 11 million men that can be mobilized if need be”35, In other words, Iran can mobilize up to half a million regular troops and several million militia. Its Quds special forces are already operating inside Iraq. U.S. Military and Allied Facilities Surrounding Iran For several years now, Iran has been conducting its own war drills and exercises. While its Air Force has weaknesses, its intermediate and long-range missiles are fully operational. Iran’s military is in a state of readiness. Iranian troop concentrations are currently within a few kilometers of the Iraqi and Afghan borders, and within proximity of Kuwait. The Iranian Navy is deployed in the Persian Gulf within proximity of U.S. and allied military facilities in the United Arab Emirates. It is worth noting that in response to Iran’s military build-up, the U.S. has been transferring large amounts of weapons to its non-NATO allies in the Persian Gulf including Kuwait and Saudi Arabia. While Iran’s advanced weapons do not measure up to those of the U.S. and NATO, Iranian forces would be in a position to inflict substantial losses to coalition forces in a conventional war theater, on the ground in Iraq or Afghanistan. Iranian ground troops and tanks in December 2009 crossed the border into Iraq without being confronted or challenged by allied forces and occupied a disputed territory in the East Maysan oil field. Even in the event of an effective Blitzkrieg, which targets Iran’s military facilities, its communications systems etc., through massive aerial bombing, using cruise missiles, conventional bunker buster bombs and tactical nuclear weapons, a war with Iran, once initiated, could eventually lead into a ground war. This is something which U.S. military planners have no doubt contemplated in their simulated war scenarios. An operation of this nature would result in significant military and civilian casualties, particularly if nuclear weapons are used. Within a scenario of escalation, Iranian troops could cross the border into Iraq and Afghanistan. In turn, military escalation using nuclear weapons could lead us into a World War III scenario, extending beyond the Middle-East – Central Asian region. In a very real sense, this military project, which has been on the Pentagon’s drawing board for more than ten years, threatens the future of humanity. Our focus in this chapter has been on war preparations. The fact that war preparations are in an advanced state of readiness does not imply that these war plans will be carried out. The U.S.-NATO-Israel alliance realizes that the enemy has significant capabilities to respond and retaliate. This factor in itself has been crucial in the decision by the U.S. and its allies to postpone an attack on Iran. Another crucial factor is the structure of military alliances. Whereas NATO has become a formidable force, the Shanghai Cooperation Organization (SCO), which constitutes an alliance between Russia and China and a number of former Soviet Republics has been significantly weakened. The ongoing U.S. military threats directed against China and Russia are intended to weaken the SCO and discourage any form of military action on the part of Iran’s allies in the case of a U.S. NATO Israeli attack. Video Interview: Michel Chossudovsky and Caroline Mailloux November 2023 Interview Notes 1. See Target Iran – Air Strikes, Globalsecurity.org, undated. 2. William Arkin, Washington Post, April 16, 2006. 3. Ibid. 4. New Statesman, February 19, 2007. 5. Philip Giraldi, Deep Background,The American Conservative August 2005. 6. U.S.CENTCOM, http://www.milnet.com/milnet/pentagon/centcom/chap1/stratgic.htm#U.S.Policy, link no longer active, archived at http://tinyurl.com/37gafu9. 7. General Wesley Clark, for further details see Chapter I. 8. See Michel Chossudovsky, Planned U.S.-Israeli Attack on Iran, Global Research, May 1, 2005. 9. Dick Cheney, quoted from an MSNBC Interview, January 2005. 10. According to Zbigniew Brzezinski. 11. Michel Chossudovsky, Unusually Large U.S. Weapons Shipment to Israel: Are the U.S. and Israel Planning a Broader Middle East War? Global Research, January 11, 2009. 12. Defense Talk.com, January 6, 2009. 13. Quoted in Israel National News, January 9, 2009. 14. Webster Tarpley, Fidel Castro Warns of Imminent Nuclear War; Admiral Mullen Threatens Iran; U.S.-Israel versus Iran-Hezbollah Confrontation Builds On, Global Research, August 10, 2010. 15. Michel Chossudovsky, Nuclear War against Iran, Global Research, January 3, 2006. 16. David Ruppe, Pre-emptive Nuclear War in a State of Readiness: U.S. Command Declares Global Strike Ca- pability, Global Security Newswire, December 2, 2005. 17. U.S. Nuclear Option on Iran Linked to Israeli Attack Threat – IPS ipsnews.net, April 23, 2010. 18. Revealed: Israel plans nuclear strike on Iran – Times Online, January 7, 2007. 19. Opponents Surprised By Elimination of Nuke Research Funds, Defense News, November 29, 2004. 20. See Michel Chossudovsky, “Tactical Nuclear Weapons” against Afghanistan?, Global Research, December 5, 2001. See also http://www.thebulletin.org/article_nn.php?art_ofn=jf03norris. 21. Jonathan Karl, Is the U.S. Preparing to Bomb Iran? ABC News, October 9, 2009. 22. Ibid. 23. ABC News, op cit, emphasis added. To consult the reprogramming request (pdf) click here. 24. See Edwin Black, “Super Bunker-Buster Bombs Fast-Tracked for Possible Use Against Iran and North Korea Nuclear Programs”, Cutting Edge, September 21, 2009. 25. See Project for a New American Century, Rebuilding America’s Defenses Washington DC, September 2000, pdf. 26. Ibid, emphasis added. 27. See Michel Chossudovsky, “Owning the Weather” for Military Use, Global Research, September 27, 2004. 28. Air Force 2025 Final Report, See also U.S. Air Force: Weather as a Force Multiplier: Owning the Weather in 2025, AF2025 v3c15-1. 29. See Mojmir Babacek, Electromagnetic and Informational Weapons:, Global Research, August 6, 2004. 30. Project for a New American Century, op cit., p. 60. 31. See Michel Chossudovsky, Iran’s “Power of Deterrence” Global Research, November 5, 2006. 32. Debka, November 5, 2006. 33. www.cnsnews.com November 3, 2006. 34. See Islamic Republic of Iran Army – Wikipedia. Featured image is from The Libertarian Institute The Globalization of War: America’s “Long War” against Humanity Michel Chossudovsky The “globalization of war” is a hegemonic project. Major military and covert intelligence operations are being undertaken simultaneously in the Middle East, Eastern Europe, sub-Saharan Africa, Central Asia and the Far East. The U.S. military agenda combines both major theater operations as well as covert actions geared towards destabilizing sovereign states. ISBN Number: 978-0-9879389-0-9 Year: 2015 Pages: 240 Pages Price: $9.40 Click here to order. Related Articles from our Archives https://www.globalresearch.ca/pre-emptive-nuclear-war-the-role-of-israel-in-triggering-an-attack-on-iran/5840256 https://telegra.ph/Nuclear-war-03-10
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  • The WHO Wants to Rule the World
    Ramesh Thakur
    The World Health Organisation (WHO) will present two new texts for adoption by its governing body, the World Health Assembly comprising delegates from 194 member states, in Geneva on 27 May–1 June. The new pandemic treaty needs a two-thirds majority for approval and, if and once adopted, will come into effect after 40 ratifications.

    The amendments to the International Health Regulations (IHR) can be adopted by a simple majority and will be binding on all states unless they recorded reservations by the end of last year. Because they will be changes to an existing agreement that states have already signed, the amendments do not require any follow-up ratification. The WHO describes the IHR as ‘an instrument of international law that is legally-binding’ on its 196 states parties, including the 194 WHO member states, even if they voted against it. Therein lies its promise and its threat.

    The new regime will change the WHO from a technical advisory organisation into a supra-national public health authority exercising quasi-legislative and executive powers over states; change the nature of the relationship between citizens, business enterprises, and governments domestically, and also between governments and other governments and the WHO internationally; and shift the locus of medical practice from the doctor-patient consultation in the clinic to public health bureaucrats in capital cities and WHO headquarters in Geneva and its six regional offices.

    From net zero to mass immigration and identity politics, the ‘expertocracy’ elite is in alliance with the global technocratic elite against majority national sentiment. The Covid years gave the elites a valuable lesson in how to exercise effective social control and they mean to apply it across all contentious issues.

    The changes to global health governance architecture must be understood in this light. It represents the transformation of the national security, administrative, and surveillance state into a globalised biosecurity state. But they are encountering pushback in Italy, the Netherlands, Germany, and most recently Ireland. We can but hope that the resistance will spread to rejecting the WHO power grab.

    Addressing the World Governments Summit in Dubai on 12 February, WHO Director-General (DG) Tedros Adhanom Ghebreyesus attacked ‘the litany of lies and conspiracy theories’ about the agreement that ‘are utterly, completely, categorically false. The pandemic agreement will not give WHO any power over any state or any individual, for that matter.’ He insisted that critics are ‘either uninformed or lying.’ Could it be instead that, relying on aides, he himself has either not read or not understood the draft? The alternative explanation for his spray at the critics is that he is gaslighting us all.

    The Gostin, Klock, and Finch Paper

    In the Hastings Center Report “Making the World Safer and Fairer in Pandemics,” published on 23 December, Lawrence Gostin, Kevin Klock, and Alexandra Finch attempt to provide the justification to underpin the proposed new IHR and treaty instruments as ‘transformative normative and financial reforms that could reimagine pandemic prevention, preparedness, and response.’

    The three authors decry the voluntary compliance under the existing ‘amorphous and unenforceable’ IHR regulations as ‘a critical shortcoming.’ And they concede that ‘While advocates have pressed for health-related human rights to be included in the pandemic agreement, the current draft does not do so.’ Directly contradicting the DG’s denial as quoted above, they describe the new treaty as ‘legally binding’. This is repeated several pages later:

    …the best way to contain transnational outbreaks is through international cooperation, led multilaterally through the WHO. That may require all states to forgo some level of sovereignty in exchange for enhanced safety and fairness.

    What gives their analysis significance is that, as explained in the paper itself, Gostin is ‘actively involved in WHO processes for a pandemic agreement and IHR reform’ as the director of the WHO Collaborating Center on National and Global Health Law and a member of the WHO Review Committee on IHR amendments.

    The WHO as the World’s Guidance and Coordinating Authority

    The IHR amendments will expand the situations that constitute a public health emergency, grant the WHO additional emergency powers, and extend state duties to build ‘core capacities’ of surveillance to detect, assess, notify, and report events that could constitute an emergency.

    Under the new accords, the WHO would function as the guidance and coordinating authority for the world. The DG will become more powerful than the UN Secretary-General. The existing language of ‘should’ is replaced in many places by the imperative ‘shall,’ of non-binding recommendations with countries will ‘undertake to follow’ the guidance. And ‘full respect for the dignity, human rights and fundamental freedoms of persons’ will be changed to principles of ‘equity’ and ‘inclusivity’ with different requirements for rich and poor countries, bleeding financial resources and pharmaceutical products from industrialised to developing countries.

    The WHO is first of all an international bureaucracy and only secondly a collective body of medical and health experts. Its Covid performance was not among its finest. Its credibility was badly damaged by tardiness in raising the alarm; by its acceptance and then rejection of China’s claim that there was no risk of human-human transmission; by the failure to hold China accountable for destroying evidence of the pandemic’s origins; by the initial investigation that whitewashed the origins of the virus; by flip-flops on masks and lockdowns; by ignoring the counterexample of Sweden that rejected lockdowns with no worse health outcomes and far better economic, social, and educational outcomes; and by the failure to stand up for children’s developmental, educational, social, and mental health rights and welfare.

    With a funding model where 87 percent of the budget comes from voluntary contributions from the rich countries and private donors like the Gates Foundation, and 77 percent is for activities specified by them, the WHO has effectively ‘become a system of global public health patronage’, write Ben and Molly Kingsley of the UK children’s rights campaign group UsForThem. Human Rights Watch says the process has been ‘disproportionately guided by corporate demands and the policy positions of high-income governments seeking to protect the power of private actors in health including the pharmaceutical industry.’ The victims of this Catch-22 lack of accountability will be the peoples of the world.

    Much of the new surveillance network in a model divided into pre-, in, and post-pandemic periods will be provided by private and corporate interests that will profit from the mass testing and pharmaceutical interventions. According to Forbes, the net worth of Bill Gates jumped by one-third from $96.5 billion in 2019 to $129 billion in 2022: philanthropy can be profitable. Article 15.2 of the draft pandemic treaty requires states to set up ‘no fault vaccine-injury compensation schemes,’ conferring immunity on Big Pharma against liability, thereby codifying the privatisation of profits and the socialisation of risks.

    The changes would confer extraordinary new powers on the WHO’s DG and regional directors and mandate governments to implement their recommendations. This will result in a major expansion of the international health bureaucracy under the WHO, for example new implementation and compliance committees; shift the centre of gravity from the common deadliest diseases (discussed below) to relatively rare pandemic outbreaks (five including Covid in the last 120 years); and give the WHO authority to direct resources (money, pharmaceutical products, intellectual property rights) to itself and to other governments in breach of sovereign and copyright rights.

    Considering the impact of the amendments on national decision-making and mortgaging future generations to internationally determined spending obligations, this calls for an indefinite pause in the process until parliaments have done due diligence and debated the potentially far-reaching obligations.

    Yet disappointingly, relatively few countries have expressed reservations and few parliamentarians seem at all interested. We may pay a high price for the rise of careerist politicians whose primary interest is self-advancement, ministers who ask bureaucrats to draft replies to constituents expressing concern that they often sign without reading either the original letter or the reply in their name, and officials who disdain the constraints of democratic decision-making and accountability. Ministers relying on technical advice from staffers when officials are engaged in a silent coup against elected representatives give power without responsibility to bureaucrats while relegating ministers to being in office but not in power, with political accountability sans authority.

    US President Donald Trump and Australian and UK Prime Ministers Scott Morrison and Boris Johnson were representative of national leaders who had lacked the science literacy, intellectual heft, moral clarity, and courage of conviction to stand up to their technocrats. It was a period of Yes, Prime Minister on steroids, with Sir Humphrey Appleby winning most of the guerrilla campaign waged by the permanent civil service against the transient and clueless Prime Minister Jim Hacker.

    At least some Australian, American, British, and European politicians have recently expressed concern at the WHO-centred ‘command and control’ model of a public health system, and the public spending and redistributive implications of the two proposed international instruments. US Representatives Chris Smith (R-NJ) and Brad Wenstrup (R-OH) warned on 5 February that ‘far too little scrutiny has been given, far too few questions asked as to what this legally binding agreement or treaty means to health policy in the United States and elsewhere.’

    Like Smith and Wenstrup, the most common criticism levelled has been that this represents a power grab at the cost of national sovereignty. Speaking in parliament in November, Australia’s Liberal Senator Alex Antic dubbed the effort a ‘WHO d’etat’.

    A more accurate reading may be that it represents collusion between the WHO and the richest countries, home to the biggest pharmaceutical companies, to dilute accountability for decisions, taken in the name of public health, that profit a narrow elite. The changes will lock in the seamless rule of the technocratic-managerial elite at both the national and the international levels. Yet the WHO edicts, although legally binding in theory, will be unenforceable against the most powerful countries in practice.

    Moreover, the new regime aims to eliminate transparency and critical scrutiny by criminalising any opinion that questions the official narrative from the WHO and governments, thereby elevating them to the status of dogma. The pandemic treaty calls for governments to tackle the ‘infodemics’ of false information, misinformation, disinformation, and even ‘too much information’ (Article 1c). This is censorship. Authorities have no right to be shielded from critical questioning of official information. Freedom of information is a cornerstone of an open and resilient society and a key means to hold authorities to public scrutiny and accountability.

    The changes are an effort to entrench and institutionalise the model of political, social, and messaging control trialled with great success during Covid. The foundational document of the international human rights regime is the 1948 Universal Declaration of Human Rights. Pandemic management during Covid and in future emergencies threaten some of its core provisions regarding privacy, freedom of opinion and expression, and rights to work, education, peaceful assembly, and association.

    Worst of all, they will create a perverse incentive: the rise of an international bureaucracy whose defining purpose, existence, powers, and budgets will depend on more frequent declarations of actual or anticipated pandemic outbreaks.

    It is a basic axiom of politics that power that can be abused, will be abused – some day, somewhere, by someone. The corollary holds that power once seized is seldom surrendered back voluntarily to the people. Lockdowns, mask and vaccine mandates, travel restrictions, and all the other shenanigans and theatre of the Covid era will likely be repeated on whim. Professor Angus Dalgliesh of London’s St George’s Medical School warns that the WHO ‘wants to inflict this incompetence on us all over again but this time be in total control.’

    Covid in the Context of Africa’s Disease Burden

    In the Hastings Center report referred to earlier, Gostin, Klock, and Finch claim that ‘lower-income countries experienced larger losses and longer-lasting economic setbacks.’ This is a casual elision that shifts the blame for harmful downstream effects away from lockdowns in the futile quest to eradicate the virus, to the virus itself. The chief damage to developing countries was caused by the worldwide shutdown of social life and economic activities and the drastic reduction in international trade.

    The discreet elision aroused my curiosity on the authors’ affiliations. It came as no surprise to read that they lead the O’Neill Institute–Foundation for the National Institutes of Health project on an international instrument for pandemic prevention and preparedness.

    Gostin et al. grounded the urgency for the new accords in the claim that ‘Zoonotic pathogens…are occurring with increasing frequency, enhancing the risk of new pandemics’ and cite research to suggest a threefold increase in ‘extreme pandemics’ over the next decade. In a report entitled “Rational Policy Over Panic,” published by Leeds University in February, a team that included our own David Bell subjected claims of increasing pandemic frequency and disease burden behind the drive to adopt the new treaty and amend the existing IHR to critical scrutiny.

    Specifically, they examined and found wanting a number of assumptions and several references in eight G20, World Bank, and WHO policy documents. On the one hand, the reported increase in natural outbreaks is best explained by technologically more sophisticated diagnostic testing equipment, while the disease burden has been effectively reduced with improved surveillance, response mechanisms, and other public health interventions. Consequently there is no real urgency to rush into the new accords. Instead, governments should take all the time they need to situate pandemic risk in the wider healthcare context and formulate policy tailored to the more accurate risk and interventions matrix.


    The lockdowns were responsible for reversals of decades worth of gains in critical childhood immunisations. UNICEF and WHO estimate that 7.6 million African children under 5 missed out on vaccination in 2021 and another 11 million were under-immunised, ‘making up over 40 percent of the under-immunised and missed children globally.’ How many quality adjusted life years does that add up to, I wonder? But don’t hold your breath that anyone will be held accountable for crimes against African children.

    Earlier this month the Pan-African Epidemic and Pandemic Working Group argued that lockdowns were a ‘class-based and unscientific instrument.’ It accused the WHO of trying to reintroduce ‘classical Western colonialism through the backdoor’ in the form of the new pandemic treaty and the IHR amendments. Medical knowledge and innovations do not come solely from Western capitals and Geneva, but from people and groups who have captured the WHO agenda.

    Lockdowns had caused significant harm to low-income countries, the group said, yet the WHO wanted legal authority to compel member states to comply with its advice in future pandemics, including with respect to vaccine passports and border closures. Instead of bowing to ‘health imperialism,’ it would be preferable for African countries to set their own priorities in alleviating the disease burden of their major killer diseases like cholera, malaria, and yellow fever.

    Europe and the US, comprising a little under ten and over four percent of world population, account for nearly 18 and 17 percent, respectively, of all Covid-related deaths in the world. By contrast Asia, with nearly 60 percent of the world’s people, accounts for 23 percent of all Covid-related deaths. Meantime Africa, with more than 17 percent of global population, has recorded less than four percent of global Covid deaths (Table 1).

    According to a report on the continent’s disease burden published last year by the WHO Regional Office for Africa, Africa’s leading causes of death in 2021 were malaria (593,000 deaths), tuberculosis (501,000), and HIV/AIDS (420,000). The report does not provide the numbers for diarrhoeal deaths for Africa. There are 1.6 million such deaths globally per year, including 440,000 children under 5. And we know that most diarrhoeal deaths occur in Africa and South Asia.

    If we perform a linear extrapolation of 2021 deaths to estimate ballpark figures for the three years 2020–22 inclusive for numbers of Africans killed by these big three, approximately 1.78 million died from malaria, 1.5 million from TB, and 1.26 million from HIV/AIDS. (I exclude 2023 as Covid had faded by then, as can be seen in Table 1). By comparison, the total number of Covid-related deaths across Africa in the three years was 259,000.

    Whether or not the WHO is pursuing a policy of health colonialism, therefore, the Pan-African Epidemic and Pandemic Working Group has a point regarding the grossly exaggerated threat of Covid in the total picture of Africa’s disease burden.

    A shorter version of this was published in The Australian on 11 March

    Published under a Creative Commons Attribution 4.0 International License
    For reprints, please set the canonical link back to the original Brownstone Institute Article and Author.

    Author

    Ramesh Thakur, a Brownstone Institute Senior Scholar, is a former United Nations Assistant Secretary-General, and emeritus professor in the Crawford School of Public Policy, The Australian National University.

    View all posts
    Your financial backing of Brownstone Institute goes to support writers, lawyers, scientists, economists, and other people of courage who have been professionally purged and displaced during the upheaval of our times. You can help get the truth out through their ongoing work.

    https://brownstone.org/articles/the-who-wants-to-rule-the-world/
    The WHO Wants to Rule the World Ramesh Thakur The World Health Organisation (WHO) will present two new texts for adoption by its governing body, the World Health Assembly comprising delegates from 194 member states, in Geneva on 27 May–1 June. The new pandemic treaty needs a two-thirds majority for approval and, if and once adopted, will come into effect after 40 ratifications. The amendments to the International Health Regulations (IHR) can be adopted by a simple majority and will be binding on all states unless they recorded reservations by the end of last year. Because they will be changes to an existing agreement that states have already signed, the amendments do not require any follow-up ratification. The WHO describes the IHR as ‘an instrument of international law that is legally-binding’ on its 196 states parties, including the 194 WHO member states, even if they voted against it. Therein lies its promise and its threat. The new regime will change the WHO from a technical advisory organisation into a supra-national public health authority exercising quasi-legislative and executive powers over states; change the nature of the relationship between citizens, business enterprises, and governments domestically, and also between governments and other governments and the WHO internationally; and shift the locus of medical practice from the doctor-patient consultation in the clinic to public health bureaucrats in capital cities and WHO headquarters in Geneva and its six regional offices. From net zero to mass immigration and identity politics, the ‘expertocracy’ elite is in alliance with the global technocratic elite against majority national sentiment. The Covid years gave the elites a valuable lesson in how to exercise effective social control and they mean to apply it across all contentious issues. The changes to global health governance architecture must be understood in this light. It represents the transformation of the national security, administrative, and surveillance state into a globalised biosecurity state. But they are encountering pushback in Italy, the Netherlands, Germany, and most recently Ireland. We can but hope that the resistance will spread to rejecting the WHO power grab. Addressing the World Governments Summit in Dubai on 12 February, WHO Director-General (DG) Tedros Adhanom Ghebreyesus attacked ‘the litany of lies and conspiracy theories’ about the agreement that ‘are utterly, completely, categorically false. The pandemic agreement will not give WHO any power over any state or any individual, for that matter.’ He insisted that critics are ‘either uninformed or lying.’ Could it be instead that, relying on aides, he himself has either not read or not understood the draft? The alternative explanation for his spray at the critics is that he is gaslighting us all. The Gostin, Klock, and Finch Paper In the Hastings Center Report “Making the World Safer and Fairer in Pandemics,” published on 23 December, Lawrence Gostin, Kevin Klock, and Alexandra Finch attempt to provide the justification to underpin the proposed new IHR and treaty instruments as ‘transformative normative and financial reforms that could reimagine pandemic prevention, preparedness, and response.’ The three authors decry the voluntary compliance under the existing ‘amorphous and unenforceable’ IHR regulations as ‘a critical shortcoming.’ And they concede that ‘While advocates have pressed for health-related human rights to be included in the pandemic agreement, the current draft does not do so.’ Directly contradicting the DG’s denial as quoted above, they describe the new treaty as ‘legally binding’. This is repeated several pages later: …the best way to contain transnational outbreaks is through international cooperation, led multilaterally through the WHO. That may require all states to forgo some level of sovereignty in exchange for enhanced safety and fairness. What gives their analysis significance is that, as explained in the paper itself, Gostin is ‘actively involved in WHO processes for a pandemic agreement and IHR reform’ as the director of the WHO Collaborating Center on National and Global Health Law and a member of the WHO Review Committee on IHR amendments. The WHO as the World’s Guidance and Coordinating Authority The IHR amendments will expand the situations that constitute a public health emergency, grant the WHO additional emergency powers, and extend state duties to build ‘core capacities’ of surveillance to detect, assess, notify, and report events that could constitute an emergency. Under the new accords, the WHO would function as the guidance and coordinating authority for the world. The DG will become more powerful than the UN Secretary-General. The existing language of ‘should’ is replaced in many places by the imperative ‘shall,’ of non-binding recommendations with countries will ‘undertake to follow’ the guidance. And ‘full respect for the dignity, human rights and fundamental freedoms of persons’ will be changed to principles of ‘equity’ and ‘inclusivity’ with different requirements for rich and poor countries, bleeding financial resources and pharmaceutical products from industrialised to developing countries. The WHO is first of all an international bureaucracy and only secondly a collective body of medical and health experts. Its Covid performance was not among its finest. Its credibility was badly damaged by tardiness in raising the alarm; by its acceptance and then rejection of China’s claim that there was no risk of human-human transmission; by the failure to hold China accountable for destroying evidence of the pandemic’s origins; by the initial investigation that whitewashed the origins of the virus; by flip-flops on masks and lockdowns; by ignoring the counterexample of Sweden that rejected lockdowns with no worse health outcomes and far better economic, social, and educational outcomes; and by the failure to stand up for children’s developmental, educational, social, and mental health rights and welfare. With a funding model where 87 percent of the budget comes from voluntary contributions from the rich countries and private donors like the Gates Foundation, and 77 percent is for activities specified by them, the WHO has effectively ‘become a system of global public health patronage’, write Ben and Molly Kingsley of the UK children’s rights campaign group UsForThem. Human Rights Watch says the process has been ‘disproportionately guided by corporate demands and the policy positions of high-income governments seeking to protect the power of private actors in health including the pharmaceutical industry.’ The victims of this Catch-22 lack of accountability will be the peoples of the world. Much of the new surveillance network in a model divided into pre-, in, and post-pandemic periods will be provided by private and corporate interests that will profit from the mass testing and pharmaceutical interventions. According to Forbes, the net worth of Bill Gates jumped by one-third from $96.5 billion in 2019 to $129 billion in 2022: philanthropy can be profitable. Article 15.2 of the draft pandemic treaty requires states to set up ‘no fault vaccine-injury compensation schemes,’ conferring immunity on Big Pharma against liability, thereby codifying the privatisation of profits and the socialisation of risks. The changes would confer extraordinary new powers on the WHO’s DG and regional directors and mandate governments to implement their recommendations. This will result in a major expansion of the international health bureaucracy under the WHO, for example new implementation and compliance committees; shift the centre of gravity from the common deadliest diseases (discussed below) to relatively rare pandemic outbreaks (five including Covid in the last 120 years); and give the WHO authority to direct resources (money, pharmaceutical products, intellectual property rights) to itself and to other governments in breach of sovereign and copyright rights. Considering the impact of the amendments on national decision-making and mortgaging future generations to internationally determined spending obligations, this calls for an indefinite pause in the process until parliaments have done due diligence and debated the potentially far-reaching obligations. Yet disappointingly, relatively few countries have expressed reservations and few parliamentarians seem at all interested. We may pay a high price for the rise of careerist politicians whose primary interest is self-advancement, ministers who ask bureaucrats to draft replies to constituents expressing concern that they often sign without reading either the original letter or the reply in their name, and officials who disdain the constraints of democratic decision-making and accountability. Ministers relying on technical advice from staffers when officials are engaged in a silent coup against elected representatives give power without responsibility to bureaucrats while relegating ministers to being in office but not in power, with political accountability sans authority. US President Donald Trump and Australian and UK Prime Ministers Scott Morrison and Boris Johnson were representative of national leaders who had lacked the science literacy, intellectual heft, moral clarity, and courage of conviction to stand up to their technocrats. It was a period of Yes, Prime Minister on steroids, with Sir Humphrey Appleby winning most of the guerrilla campaign waged by the permanent civil service against the transient and clueless Prime Minister Jim Hacker. At least some Australian, American, British, and European politicians have recently expressed concern at the WHO-centred ‘command and control’ model of a public health system, and the public spending and redistributive implications of the two proposed international instruments. US Representatives Chris Smith (R-NJ) and Brad Wenstrup (R-OH) warned on 5 February that ‘far too little scrutiny has been given, far too few questions asked as to what this legally binding agreement or treaty means to health policy in the United States and elsewhere.’ Like Smith and Wenstrup, the most common criticism levelled has been that this represents a power grab at the cost of national sovereignty. Speaking in parliament in November, Australia’s Liberal Senator Alex Antic dubbed the effort a ‘WHO d’etat’. A more accurate reading may be that it represents collusion between the WHO and the richest countries, home to the biggest pharmaceutical companies, to dilute accountability for decisions, taken in the name of public health, that profit a narrow elite. The changes will lock in the seamless rule of the technocratic-managerial elite at both the national and the international levels. Yet the WHO edicts, although legally binding in theory, will be unenforceable against the most powerful countries in practice. Moreover, the new regime aims to eliminate transparency and critical scrutiny by criminalising any opinion that questions the official narrative from the WHO and governments, thereby elevating them to the status of dogma. The pandemic treaty calls for governments to tackle the ‘infodemics’ of false information, misinformation, disinformation, and even ‘too much information’ (Article 1c). This is censorship. Authorities have no right to be shielded from critical questioning of official information. Freedom of information is a cornerstone of an open and resilient society and a key means to hold authorities to public scrutiny and accountability. The changes are an effort to entrench and institutionalise the model of political, social, and messaging control trialled with great success during Covid. The foundational document of the international human rights regime is the 1948 Universal Declaration of Human Rights. Pandemic management during Covid and in future emergencies threaten some of its core provisions regarding privacy, freedom of opinion and expression, and rights to work, education, peaceful assembly, and association. Worst of all, they will create a perverse incentive: the rise of an international bureaucracy whose defining purpose, existence, powers, and budgets will depend on more frequent declarations of actual or anticipated pandemic outbreaks. It is a basic axiom of politics that power that can be abused, will be abused – some day, somewhere, by someone. The corollary holds that power once seized is seldom surrendered back voluntarily to the people. Lockdowns, mask and vaccine mandates, travel restrictions, and all the other shenanigans and theatre of the Covid era will likely be repeated on whim. Professor Angus Dalgliesh of London’s St George’s Medical School warns that the WHO ‘wants to inflict this incompetence on us all over again but this time be in total control.’ Covid in the Context of Africa’s Disease Burden In the Hastings Center report referred to earlier, Gostin, Klock, and Finch claim that ‘lower-income countries experienced larger losses and longer-lasting economic setbacks.’ This is a casual elision that shifts the blame for harmful downstream effects away from lockdowns in the futile quest to eradicate the virus, to the virus itself. The chief damage to developing countries was caused by the worldwide shutdown of social life and economic activities and the drastic reduction in international trade. The discreet elision aroused my curiosity on the authors’ affiliations. It came as no surprise to read that they lead the O’Neill Institute–Foundation for the National Institutes of Health project on an international instrument for pandemic prevention and preparedness. Gostin et al. grounded the urgency for the new accords in the claim that ‘Zoonotic pathogens…are occurring with increasing frequency, enhancing the risk of new pandemics’ and cite research to suggest a threefold increase in ‘extreme pandemics’ over the next decade. In a report entitled “Rational Policy Over Panic,” published by Leeds University in February, a team that included our own David Bell subjected claims of increasing pandemic frequency and disease burden behind the drive to adopt the new treaty and amend the existing IHR to critical scrutiny. Specifically, they examined and found wanting a number of assumptions and several references in eight G20, World Bank, and WHO policy documents. On the one hand, the reported increase in natural outbreaks is best explained by technologically more sophisticated diagnostic testing equipment, while the disease burden has been effectively reduced with improved surveillance, response mechanisms, and other public health interventions. Consequently there is no real urgency to rush into the new accords. Instead, governments should take all the time they need to situate pandemic risk in the wider healthcare context and formulate policy tailored to the more accurate risk and interventions matrix. The lockdowns were responsible for reversals of decades worth of gains in critical childhood immunisations. UNICEF and WHO estimate that 7.6 million African children under 5 missed out on vaccination in 2021 and another 11 million were under-immunised, ‘making up over 40 percent of the under-immunised and missed children globally.’ How many quality adjusted life years does that add up to, I wonder? But don’t hold your breath that anyone will be held accountable for crimes against African children. Earlier this month the Pan-African Epidemic and Pandemic Working Group argued that lockdowns were a ‘class-based and unscientific instrument.’ It accused the WHO of trying to reintroduce ‘classical Western colonialism through the backdoor’ in the form of the new pandemic treaty and the IHR amendments. Medical knowledge and innovations do not come solely from Western capitals and Geneva, but from people and groups who have captured the WHO agenda. Lockdowns had caused significant harm to low-income countries, the group said, yet the WHO wanted legal authority to compel member states to comply with its advice in future pandemics, including with respect to vaccine passports and border closures. Instead of bowing to ‘health imperialism,’ it would be preferable for African countries to set their own priorities in alleviating the disease burden of their major killer diseases like cholera, malaria, and yellow fever. Europe and the US, comprising a little under ten and over four percent of world population, account for nearly 18 and 17 percent, respectively, of all Covid-related deaths in the world. By contrast Asia, with nearly 60 percent of the world’s people, accounts for 23 percent of all Covid-related deaths. Meantime Africa, with more than 17 percent of global population, has recorded less than four percent of global Covid deaths (Table 1). According to a report on the continent’s disease burden published last year by the WHO Regional Office for Africa, Africa’s leading causes of death in 2021 were malaria (593,000 deaths), tuberculosis (501,000), and HIV/AIDS (420,000). The report does not provide the numbers for diarrhoeal deaths for Africa. There are 1.6 million such deaths globally per year, including 440,000 children under 5. And we know that most diarrhoeal deaths occur in Africa and South Asia. If we perform a linear extrapolation of 2021 deaths to estimate ballpark figures for the three years 2020–22 inclusive for numbers of Africans killed by these big three, approximately 1.78 million died from malaria, 1.5 million from TB, and 1.26 million from HIV/AIDS. (I exclude 2023 as Covid had faded by then, as can be seen in Table 1). By comparison, the total number of Covid-related deaths across Africa in the three years was 259,000. Whether or not the WHO is pursuing a policy of health colonialism, therefore, the Pan-African Epidemic and Pandemic Working Group has a point regarding the grossly exaggerated threat of Covid in the total picture of Africa’s disease burden. A shorter version of this was published in The Australian on 11 March Published under a Creative Commons Attribution 4.0 International License For reprints, please set the canonical link back to the original Brownstone Institute Article and Author. Author Ramesh Thakur, a Brownstone Institute Senior Scholar, is a former United Nations Assistant Secretary-General, and emeritus professor in the Crawford School of Public Policy, The Australian National University. View all posts Your financial backing of Brownstone Institute goes to support writers, lawyers, scientists, economists, and other people of courage who have been professionally purged and displaced during the upheaval of our times. You can help get the truth out through their ongoing work. https://brownstone.org/articles/the-who-wants-to-rule-the-world/
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    The WHO Wants to Rule the World ⋆ Brownstone Institute
    The World Health Organisation (WHO) will present two new texts for adoption by its governing body, the World Health Assembly comprising delegates from 194 member states, in Geneva on 27 May–1 June.
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  • DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA

    Rebekah Barnett
    Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can.

    The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells.

    Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say.

    And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say.

    However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA.

    TLDR

    1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable)

    2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient)

    3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination

    4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA.
    Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process.

    McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.”

    Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients.

    But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan.

    While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration.

    Now, the first results are in.

    In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine.

    The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites.

    “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says.

    “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.”

    To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls.

    The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan.

    Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA.

    This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with.


    Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack
    Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA.

    “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.”

    Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan.


    Source: Kevin McKernan’s Substack
    Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line.

    You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’

    ‘Major advance,’ but clinical implications are limited

    McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.”

    “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries.

    The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells.

    McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately.

    At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan.

    The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety.

    Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English).

    LNPs deliver contaminant DNA straight to the cells

    A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur.

    This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes.

    This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems.


    Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021
    From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.”

    It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis.

    Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines.

    Regulators unconcerned

    I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment.

    The TGA did not address the new findings, but a spokesperson from the TGA responded,

    “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.”

    However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims.

    Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised.

    Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted.

    In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year.

    Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories.

    Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning.

    Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further.

    The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk.

    ‘No excuse’ for ignoring ‘screaming hot signal’

    Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan.

    Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.”

    “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?”

    There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years.

    “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.”


    Source: National Human Genome Research Institute
    DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination.

    “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.”

    Scientists pick up regulators’ slack

    In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton.

    “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.”

    Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites.

    In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in.

    “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said.

    McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present.

    Decentralisation the future of science?

    McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust.

    “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan.

    “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“

    In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world.


    Source: X
    For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation.

    “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan.

    Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet.

    Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct.


    Source: X
    In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.”

    But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa.

    Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not.

    The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received.

    View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files.

    Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina.

    Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account.


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    1
    From an article I wrote for Umbrella News on this topic last year:

    The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News,

    “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.”

    “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.”

    With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected).

    As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims.

    The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken.

    Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed.


    https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows It also appears that the contamination enters the cell nucleus and integrates with human DNA Rebekah Barnett Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can. The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells. Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say. And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say. However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA. TLDR 1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable) 2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient) 3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination 4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA. Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process. McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.” Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients. But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan. While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration. Now, the first results are in. In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine. The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites. “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says. “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.” To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls. The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan. Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA. This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with. Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA. “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.” Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan. Source: Kevin McKernan’s Substack Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line. You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’ ‘Major advance,’ but clinical implications are limited McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.” “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries. The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells. McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately. At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan. The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety. Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English). LNPs deliver contaminant DNA straight to the cells A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur. This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes. This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems. Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021 From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.” It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis. Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines. Regulators unconcerned I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment. The TGA did not address the new findings, but a spokesperson from the TGA responded, “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.” However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims. Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised. Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted. In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year. Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories. Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning. Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further. The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk. ‘No excuse’ for ignoring ‘screaming hot signal’ Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan. Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.” “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?” There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years. “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.” Source: National Human Genome Research Institute DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination. “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.” Scientists pick up regulators’ slack In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton. “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.” Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites. In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in. “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said. McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present. Decentralisation the future of science? McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust. “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan. “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“ In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world. Source: X For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation. “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan. Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet. Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct. Source: X In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.” But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa. Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not. The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received. View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files. Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina. Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account. To support my work, make a one-off contribution to DDU via my Kofi account and/or subscribe. Thanks! Follow me on X Follow me on Instagram 1 From an article I wrote for Umbrella News on this topic last year: The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News, “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.” “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.” With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected). As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims. The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken. Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed. https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    NEWS.REBEKAHBARNETT.COM.AU
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA
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  • BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy
    donshafi911
    BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy

    January 6, 2024

    VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel
    $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts

    Source: Embassy of Israel, Washington, D.C. and US Department of State.

    In the cover image, the Canadian researcher Jessica Rose, author of an excellent biochemical analysis of an article from the University of Cambridge commenting a study by some of its researchers on the toxicity of manipulated human nucleoside in mRNA genetic sera

    by Fabio Giuseppe Carlo Carisio

    VERSIONE IN ITALIANO

    «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell».

    With this phrase to be engraved in the history of the massive Covid vaccination campaign, the esteemed Canadian researcher, biochemist, immunologist and molecular biologist Jessica Rose (Source 1), author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridge in relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule” because it is a biological human component modified twice in the laboratory. (Source 1).

    UPDATE! Florida State Surgeon General Calls for Halt of mRNA Vaccines due to Dangerous, Oncogenes DNA Fragments
    Author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridgein relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule”because it is a biological human component modified twice in the laboratory.

    Billions of Dangerous Spike DNA’s Molecules inside Covid mRNA Vaccines. They can Reproduce the Toxic Protein in Human Cells for a Long Time
    This is the double alteration of Uridinetransformed into Pseudourine with the first synthetic biochemical alteration and then into N1-methylpseudouridine initialed “m1Ψ” as an acronym for N1-methyl-Ψ in which the Greek letter “Psi” was used to name Psueudoridine .

    Uridine is an organic compound, nucleoside,made up of the coupling of a molecule of ribose and one of uracil. Uracil is one of the two pyrimidine nitrogenous bases that form the nucleotides of RNA nucleic acid.



    This manipulation was designed by the Hungarian biochemist Katalin Karikó,awarded the 2023 Nobel Prize for Medicine precisely for having laid the foundations of mRNA vaccines, in order to “deceive” human cells into recognizing the synthetic mRNA as harmless human RNA …

    I apologize to the biochemistry experts for any transcription mistakes I may make trying to translate from a difficult chemical language the portentous scientific essence of the abundant technical quotations in the article published by Rose on her Substack, from which we will only extrapolate its introduction.

    Bombshell from US! FDA “Hides” Toxicity on DNA Fragments inside mRNA Vaccines despite Danger of Cancer Highlighted in its Guidance too
    Martin: “Pseudouridine Killer in the Vaccines for Depopulation”
    This analysis comes surprisingly providential as on Gospa News International we have just reported the summary of a conference by the famous patent expert David E. Martin in which he narrated in recent weeks the story of SARS-Cov-2 as a bacteriological weapon built in 58 years of military research on coronaviruses and that of mRNA vaccines, in his opinion, knowingly spread in a mass experiment for the search for vaccines against HIV-AIDS and cancer but also aimed at global depopulation.

    WUHAN-GATES – 73. Half of Century of Covert Bioweapon Development Leading to Fauci’s SARS-Cov-2 and to mRNA Lethal Vaccines
    In a very detailed article the American osteopath doctor Joseph Mercola wrote that «Martin points out that even if they don’t unleash any other bioweapons, the desired death toll may still be achieved, because they used pseudouridine in the mRNA shots, which is causing “turbo cancers”».

    Because: «Pseudouridine suppresses cancer-controlling agents and promotes oncogenic activity in the body, and this has been known since 2018, so its inclusion was hardly an accident. It’s a conspiracy, alright. But not a conspiracy theory in the dismissive sense. It’s a global conspiracy by identifiable agents who have, for nearly 60 years, plotted to commit, and profit from, the greatest genocide the world has ever seen, while hiding behind the false veneer of “public health.”».
    Well today, both the University of Cambridge and other authoritative scientists from around the world implicitly confirm that all those vaccinated with Covid mRNA with Moderna’s Spikevax and Pfizer-Biontech’s Comirnaty have been and continue to be unpaid and, above all, unaware human guinea pigs.

    Precisely because of this altered nucleoside…

    The Disturbing Article from Cambridge University
    The comment by the researcher Rose that we reported in the incipit of the article referred to the text of the University of Cambridge(Source 2) in relation to the study “N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting” by Mulroney et al.published on December 6, 2023 by Nature after more than a month of review.



    «Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses» is the eloquent title of the scientific text published by the British university.

    «The latest developments, led by biochemist Professor Anne Willis and immunologist Dr James Thaventhiran from the MRC Toxicology Unit at the University of Cambridge, build upon previous advances to ensure the prevention of any safety issues linked with future mRNA-based therapeutics. Their report is published today in the journal Nature» we read in the unsigned article.

    «The researchers identified that bases with a chemical modification called N1-methylpseudouridine – which are currently contained in mRNA therapies – are responsible for the ‘slips’ along the mRNA sequence» adds the university website.
    In collaboration with researchers at the Universities of Kent, Oxford and Liverpool, the MRC Toxicology Unit team«tested for evidence of the production of ‘off-target’ proteins in people who received the mRNA Pfizer vaccine against COVID-19. They found an unintended immune response occurred in one third of the 21 patients in the study who were vaccinated – but with no ill-effects, in keeping with the extensive safety data available on these COVID-19 vaccines».

    SCIENCE Magazine Finally Admitted the mRNA Vaccines Dangerous Side Effects! Shots linked to Long Covid, Neurologic Damages and POTS
    Despite disturbing the article already appears biased as it is aimed at “minimizing” the adverse reactions, even lethal one, that are accumulating in pharmacovigilance systems around the world, which have been confirmed by an alarming article in the journal Science, by the regulatory bodies from all over the world (EMA, FDA, etc.) and which led Moderna and Pfizer-Biontech to include the risk of lethal myocarditis in the information leaflets of their genetic drugs…

    7 EURODEPUTATI CHIEDONO IL RITIRO DEI VACCINI COVID. Per Miocarditi Letali, Malori Improvvisi e Sicurezza Incerta nei Fragili
    British Study: “Incorrect mRNA Translation may Increase Toxicity”
    But it is the same authors of the study whose first signatory is Thomas E. Mulroney (Source 3), associate researcher of the Toxicology Unit of the MRC in Cambridge, who wrote the shocking considerations from a biochemical point of view in the conclusions.

    «We show that 1-methylΨ is a modified ribonucleotide that significantly increases +1 ribosomal frameshifting during mRNA translation and that cellular immunity to +1 frameshifted products can occur following vaccination with mRNA containing 1-methylΨ. To our knowledge, this is the first report that mRNA modification affects ribosomal frameshifting. Alongside this impact on host T cell immunity, the off-target effects of ribosomal frameshifting could include increased production of new B cell antigens».




    And they further add:

    «These findings are of particular importance to our fundamental understanding of how ribonucleotide modification affects mRNA translation, and for designing and optimizing future mRNA-based therapeutics to avoid mistranslation events that may decrease efficacy or increase toxicity».
    We will not delve further into the technical references but return to the analysis published by Jessica Rose in her Substack, making an extreme summary of it and advising professionals to read the text full of important images.

    Billions of DNA Fragments of Toxic Spike Protein and SV40 gene in the mRNA Vaccines. New Study: “They may Cause Turbo-Cancer”
    Let’s start with the comment added under the research published by Nature by her together with David Wiseman, L. Maria Gutschi, David J. Speicher, Kevin McKernan.

    Alongside the Canadian biologist they were already co-authors of the study “DNA fragments detected in the monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: exploratory dose-response relationship with serious adverse events” which induced the EMA to confess that Pfizer hid the use of the very dangerous SV40 gene in its vaccine, which can cause tumors.

    The same research encouraged the bioimmunologist Robert Malone to denounce the presence of the antibiotic resistance gene in the Moderna one, pointing out also that the pharmaceutical company was aware of the tumor risks of mRNA biotechnology as reported in its own patent.

    Bomba Mondiale! “NEI VACCINI COVID GENE DI RESISTENZA AGLI ANTIBIOTICI”. Studio Spagnolo lo Conferma. Ministro Schillaci lo CELA nell’Allarme Morti AMR
    We have written extensively about these topics in three investigations, one of which – on antibiotic resistance gene – is a world exclusive.

    Alarm of American Scientists for the New Research
    Let us therefore see the content of the comment by Rose and colleagues (Source 1)on Cambridge’s research:

    The paper provides evidence for the formation “off-target” or unintended proteins following vaccination with BNT162b2 due to frameshifting. Given the proposed mechanism, a similar problem is likely to exist for the Moderna product.
    While the authors have not isolated samples of these proteins from vaccinated patients or animals, their existence is evidenced by the specific cellular immune responses elicited to frameshifted proteins the authors synthesized. It is not clear why B cell – antibody responses were not studied.
    The authors state that “Although there is no evidence that frameshifted products in humans generated from BNT162b2 vaccination are associated with adverse outcomes.”
    BOMBSHELL: mRNA COVID jabs can Damage Children’s Immune Response to OTHER Viruses as well, Study finds
    It is unclear how it is possible to make this statement, given:
    • The small number of vaccinated subjects (n=21) providing samples.
    • This was not a controlled trial.
    • None of these subjects had reported undue effects of vaccination. Accordingly, the sample is subject to selection bias.
    • The toxicology of these unintended proteins must be studied.
    • The authors acknowledge the misdirected immunity “has huge potential to be harmful.”
    Translated into simpler words, no one has verified the selection methods of the samples which may have been chosen precisely because they did not have serious adverse reactions.

    SPIKE-DEMIC among Vaccinated: 83 % hit by PCVS Syndrome. Indian Study confirmed Gates, Big Pharma’s Health Disaster
    Furthermore, in the interests of expertise we read that the two Cambridge scientists Thomas E. Mulroney and Anne E. Willis «are inventors of a pending patent application (2305297.0) relating to mRNA technology» while in the information on the authors it is discovered that Alexander J Mentzer works at the Wellcome Center for Human Genetics, University of Oxford.

    Wellcome, with the Bill & Melinda Gates Foundation and the World Economic Forum, is among the founders of the Ngo CEPI(Coalition for Epidemic Preparedness Innovations) which has already launched the SKYCovion vaccine together with the London-based GSK, managed by CEO Emma Walmsley who is also director of Microsoft, and SK Bioscience.

    WUHAN-GATES – 73. BILL III A CACCIA DI CAVIE UMANE PER VACCINO COVID COREANO. “Genotossicità non Studiata” ma OMS & UK danno OK a SkyCovione con Spike Tossica e Adiuvante GSK da Pericoloso Squalene
    But let’s go back to the analysis made by Jessica Rose on the Cambridge researchers’ study: «The authors write that N1-methylpseudouridine affects the fidelity of mRNA translation via ribosome stalling that induces frameshifting. Frameshifting results in the production multiple, unique and potentially aberrant proteins».

    «The modified mRNAs for use in the COVID-19 products were codon-optimized for maximal protein expression in humans. Codon optimization, or synonymous codon replacement, rests on the idea that one can induce mutations throughout a gene of interest (like spike) based on an organism’s (like humans) codon usage bias, to increase translational efficiency and protein expression without altering the sequence of the protein. But, it is well-known that codon-optimization can lead to protein conformation, folding and stability problems».
    COVID: SCOPERTA LA PROTEINA CHE RIVELA I LETALI COAGULI DI SANGUE. Ma Nessuno Indaga sulla Correlazione coi Vaccini
    The Canadian immunologist further notes:

    «Codon optimization could affect protein conformation, folding and stability, change post-translational modification sites and even affect protein function.Different rates of translation by different tRNAs, including those that exhibit wobble base-pairing (a tRNA that can recognize multiple synonymous codons) may actually be critical for determining the rate of translation. The ribosome may slow and pause during elongation which may actually be necessary for proper protein folding. Therefore, codon optimization may disrupt the fine-tuned timing of translation and ultimately protein function».
    The Prophetic Seneff Study on Autoimmune and Neurocerebral Damage
    He then refers to other studies that had reported the dangers of this biochemical manipulation (Source 1):

    «Codon optimization can also lead to misfolding of mRNAs due to increased Guanine/Cytosine (GC content). Please read McKernan et al.’s preprint, Xia et al.’s paper and Seneff et al.’s paper to learn more about potential problems relating to codon optimization and GC content changes. The latter group write: Synonymous codon replacement also results in a change in the multifunctional regulatory and structural roles of resulting proteins».
    ONE in THREE Covid Vaccinated with Neurological Complications. Alarming Study from Italian National Research Council
    The risks to the human organism are clearly highlighted:

    «There is, in fact, a significant enrichment of GC content (17% and 25% enrichments as per Pfizer and Moderna, respectively, as compared to SARS-CoV-2) as a result of the codon optimization that was done, and this can lead to “dysregulation of the G4-RNA-protein binding system and a wide range of potential disease-associated cellular pathologies including suppression of innate immunity, neurodegeneration, and malignant transformation”. Increased GC content significantly alters mRNA secondary structure as well, and this can also lead to ribosomal pausing or stalling».
    These considerations were expressed in a study published by illustrious scientists such as Stephanie Seneff, Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA, USA, Greg Nigh, Immersion Health, Portland, OR, USA, Anthony M. Kyriakopoulos, Nasco AD Biotechnology Laboratory, Department of Research and Development, Piraeus, Greece and Peter A. McCullough, for Health Foundation, Tucson, AZ, USA, which was the subject of enormous censorship by specialized medical journals but we published in Gospa News thanks to an excellent summary by Dr. Mercola.

    Dangerous RNA Manipulation with N1-methyl-Ψ
    Below are the quotes from Seneff et al.(Source 4) useful for understanding the connection with uridine modified in N1-methyl-Ψ: «The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein».

    «However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance».
    The COVID Jabs’ Mechanisms of Injury: Sudden Death, Blood Cloths, Human Mad Cow and Autoimmune Diseases
    In the study entitled “Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs” the scientists added:

    «These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health».
    The late biologist Luc Montagnier, in a study published posthumously by his research friends Jean-Claude Perez and Claire Moret-Chalmin with a review contribution from Seneff biophysics, proved without a shadow of a doubt the correlation between killer prions caused by vaccines and rapid deaths for neurocerebral Creutzfeldt-Jacob disease, human mad cow disease.

    PRIONS as KILLERS: 25 Deaths due to a New Mad-Cow from Covid Vaccines. Shocking Research by Montagnier (RIP), Perez & Moret-Chalmin on CJD Brain Damages
    In detail Seneff and the other scientists also refer to specific alterations:

    «Impaired type I IFN signaling is linked to many disease risks, most notably cancer, as type I IFN signaling suppresses proliferation of both viruses and cancer cells by arresting the cell cycle, in part through upregulation of p53, a tumor suppressor gene, and various cyclin- dependent kinase inhibitors (Musella et al., 2017; Matsuoka et al., 1998). IFNα also induces major histocompatibility (MHC) class 1 antigen presentation by tumor cells, causing them to be more readily recognized by the cancer surveillance system (Heise et al., 2016)».
    They then delve into the problem of the uridine molecule.

    To understand its importance we report a note from Rose: «Pseudouridines (Ψs) are a normal and essential part of our biology. They have been called the 5th nucleotide, in fact, and “are a ubiquitous constituent of structural RNA (transfer, ribosomal, small nuclear (snRNA) and small nucleolar), and present in coding RNA, across the three phylogenetic domains of life”and “accounts for about 1.4% of all bases in human rRNAs”».

    “mRNA COVID-19 Vaccines are Like Gene Therapy Products” French Study highlighted Omitted Controls on Genotoxicity
    Here’s what Seneff and his colleagues wrote about vaccines:

    «A breakthrough came when it was discovered experimentally that the mRNA coding for the spike protein could be modified in specific ways that would essentially fool the human cells into recognizing it as harmless human RNA. A seminal paper by Karikó et al. (2005) demonstrated through a series of in vitro experiments that a simple modification to the mRNA such that all uridines were replaced with pseudouridine could dramatically reduce innate immune activation against exogenous mRNA».

    Cancer Risk pointed out by the Nobel Inventor of mRNA Vaccines
    Precisely for this discovery, Hungarian researcher Katalin Karikó, long-time at Biontech, recently received the Nobel Prize for Medicine together with her American colleague Drew Weissman, although both warned of the dangers of the new mRNA biotechnology.

    Medicine Nobel to mRNA Covid Vaccines’ Scientists, both Sponsored by Gates, Fauci and Zuckerberg
    In particular, on January 6, Karikó declared to the German newspaper Welt (Source 5):

    «Every day I receive many emails from people who write to me about their experiences. One woman wrote to me that two days after the vaccination she developed a large lump in her breast. Vaccination caused cancer, it was her conclusion. But the cancer was already there, only vaccination gave an extra boost to the immune system, so that the immune defense cells rushed in large numbers towards the enemy».



    The Gospa News investigations on Turbo-Cancer based now on seven published scientific studies have highlighted a very strong correlation between mRNA gene sera and the appearance or reactivation of tumor phenomena with abnormal degeneration resulting in lethal outcomes.

    TURBO-CANCER – 2. Many Lethal/Serious Cases and New Researches on Covid mRNA Vaccines Risks. Melatonin Hope…
    Karikó herself adds: «Vaccination provides a strong boost to the immune system. It can happen that a dormant infection breaks out in people with an already weakened immune system. The extent to which this is the case for shingles will need to be examined more closely».

    Gospa News did so by discovering 27 thousand cases of Herpes Zoster, in the European Union only, as adverse reactions to vaccines reported by EMA pharmacovigilance database even in children, who are more exposed to damage to the natural immune system as confirmed by recent research.

    Esclusivo! EPIDEMIA DI HERPES DOPO I VACCINI COVID. 27mila Casi nell’UE: 31 Morti da Zoster. Lo Studio: “Per danni al Sistema Immunitario”
    Let’s go back to Seneff’s conclusions:

    «Andries et al. (2015) later discovered that 1-methylpseudouridine as a replacement for uridine was even more effective than pseudouridine and could essentially abolish the TLR response to the mRNA, preventing the activation of blood-derived dendritic cells. This modification is applied in both the mRNA vaccines on the market (Park et al., 2021)».
    To put it simply, the dendritic cell plays the role of sentinel and if it senses the presence of a pathogen in the body, it stimulates the immune response of B and T lymphocytes, specific against that antigen. If its action is limited or suppressed, it may become incapable of dealing with viral or bacterial enemies but also tumor dangers.

    Critical Role of Pseudouridine in mRNA Vaccines
    A study published by Pedro Morais, Director (Pseudouridylation Technology) ProQR Therapeutics, Leiden, Netherlands, and by Department of Biochemistry and Biophysics, Center for RNA Biology, University of Rochester Medical Center, Rochester, NY, US, entitled “The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines” highlighted the fundamental role of the laboratory alteration of this protein in the Comirnaty and Spikevax genetic sera (source 6).

    «Both consisted of N1-methyl-pseudouridine-modified mRNA encoding the SARS-COVID-19 Spike protein and were delivered with a lipid nanoparticle (LNP) formulation. Because the delivery problem of ribonucleic acids had been known for decades, the success of LNPs was quickly hailed by many as the unsung hero of COVID-19 mRNA vaccines».
    “European Medicines Agency Knew Toxicity of Pfizer Covid Vaccine”. Bombshell Study Published in US by an Italian BioChemist on Dangers mRNA-LNPs
    But the scholars, one of whom has a clear conflict of interest because he is director of the Pseudouridylation Technology project, have highlighted another very interesting fact:

    «However, the clinical trial efficacy results of the Curevac mRNA vaccine (CVnCoV) suggested that the delivery system was not the only key to the success. CVnCoV consisted of an unmodified mRNA (encoding the same spike protein as Moderna and Pfizer-BioNTech’s mRNA vaccines) and was formulated with the same LNP as Pfizer-BioNTech’s vaccine (Acuitas ALC-0315).However, its efficacy was only 48%. This striking difference in efficacy could be attributed to the presence of a critical RNA modification (N1-methyl-pseudouridine) in the Pfizer-BioNTech and Moderna’s mRNA vaccines (but not in CVnCoV)».
    “Toxic Nanoforms inside Pfizer-Biontech Covid Vaccine”. Vital Study by Italian Biochemist on US Journal of Virology highlights an Alleged Crime
    However, the same researchers highlight a significant note:

    «The intrinsic immunogenicity of non-modified mRNA was once considered a potential advantage for its use in vaccines(Ishii and Akira, 2005) as it would encode the antigen and concomitantly serve as an adjuvant while permitting a low dose. In fact, the unmodified COVID-19 mRNA vaccine candidate in late-stage clinical trials (CVnCoV, developed by Curevac) had a maximum dose of 12 µg».
    Curevac was developed by Curevac NV of Tubingen, together with the Ngo CEPI founded by Bill Gates with Wellcome and WEF, which initiated an authorization process before the CHMP committee of the European Medicines Agency (EMA) but withdrew it due to its low efficacy on October 12, 2021 (source 7) in view of the arrival of a new pharmacological product developed with GSK financed by Gates himself.

    MINISTRO SCHILLACI SPECULA SU BIG PHARMA FINANZIATA DA GATES. €700mila Investiti in Biomediche USA che Testano anche Vaccini DNA Covid
    Here is another cryptic phrase in which we talk about the “safety” of vaccines, implicitly implying that it is not clear in the current vaccines which therefore make all those who take them into “human guinea pigs”from the laboratory as the immunologist Rose clearly highlights in her final bioethical considerations.

    Rose: “Unpredictable Health Effects of Manipulated Codons”
    «Ehden Biber also wrote a great article about the pitfalls of codon optimization that you can read here. In a Nature article published in 2011 entitled: “Breaking the silence”, the author writes on the potential danger of fiddling with codons in therapeutic proteins whereby it “could have unpredictable effects on people’s health”»

    Rose wrote in her comment on the Cambridge research quoting many sentences by scientific journalist Alla Katsnelson which we report below.

    Bombshell! Texas Attorney General sues Pfizer on Covid Vaccine Efficacy and Conspiring
    In detail, the Canadian researcher adds:

    «She points to a study where the authors show that a synonymous codon change found in the most common form of cystic fibrosis results in mRNA misfolding. (Keep this in mind.) She also points out that in the context of the multi-drug resistance 1 gene (MDR1) (the gene that encodes P-glycoprotein), that a codon change may interfere with the pauses that characterize RNA passing through the ribosome, thereby changing how the growing amino acid chain folds».

    «But perhaps the most timely and spine-tingly relevant statement in this article is found at the end, and I quote: “At the moment, companies developing recombinant therapies must verify that the DNA sequence designed by their scientists is the one that’s producing their proteins, but they aren’t required to note how different that is from the native genetic code”».
    European Regulator: Pfizer Hid Dangerous Cancer Gene! It Kept Secret the SV40 DNA Sequence In COVID-19 Vaccine
    We do not have any guidance with regard to the [DNA] sequence,” Kimchi-Sarfaty notes.

    While it was the Italian bioimmunologist Mauro Mantovani who demonstrated how the “double Proline” inserted in mRNA vaccines makes the toxic Spike protein dangerously persistent in the human body.

    «That’s one piece of data that could be tracked by the system she is proposing. Such knowledge, in turn, could ultimately help define better strategies for optimization and possibly even make biologic drugs safer for people» adds Alla Katsnelson while the immunologist asks herself a question:

    «I wonder if the FDA ever took her advice to track the differences in codons and the resulting potential adverse effects?»
    Covid Vaccines Killer Pathologies in a Name Only: Spikeopathy! Huge, Chilling Study on mRNA Genic Serums’ Serious Adverse Reactions
    Therefore Rose quoted the article which we analyzed before:

    «In addition to our comment on the Nature paper, a University of Cambridge write-up entitled: Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses was penned. They make it clear that the most relevant conclusion from the Nature paper is that we can make more products similarly insanely dangerous as the ones pumped into billions of bodies because we can simply ‘reduce the production of frameshifted products’ by ‘synonymous targeting of slippery sequences’».

    So she wrote her milestone sentence:

    «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell».
    Moderna AWARE that mRNA Jabs cause CANCER due to DNA Fragments. Malone Unveils Patent
    The Canadian molecular biologist concludes before going into detail about a biochemical analysis that is too technical for non-experts:

    «The manufacturers might have thought to explore options to prevent potentially harmful responses from their products prior to injecting billions of people with them. It is criminal that these products continue to be forced onto newborns and infants by mandate, to this day».
    And then she report an emblematic quote about the risks of “Fooling with Mother Nature” by an evolutionary cell biologist at the University of Chicago: “Please do not monkey with these sites; they are optimized for some reason”, in reference to codon bias in mammals.

    Fabio Giuseppe Carlo Carisio

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    MAIN SOURCES

    SOURCE 1 – JESSICA ROSE – That Substack about N1-methylpseudouridines and frameshifting

    SOURCE 2 – UNIVERSITY OF CAMBRIDGE – Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses

    SOURCE 3 – NATURE – N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting

    SOURCE 4– PUBMED – Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs

    SOURCE 5 – WELT – “Das ist der wirkliche Grund, warum man unter neuen Varianten nicht mehr so krank wird“

    SOURCE 6 – FRONTIERS IN – The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines

    SOURCE 7 – EMA ends rolling review of CVnCoV COVID-19 vaccine following withdrawal by CureVac AG

    Fabio G. C. Carisio

    Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal.

    His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more…

    Most popolar investigation on VT is:

    Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon

    Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting.

    For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime.

    With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians.

    In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence.

    In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates

    His investigations was quoted also by The Gateway Pundit, Tasnim and others

    He worked for many years for the magazine Art & Wine as an art critic and curator.

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    https://www.vtforeignpolicy.com/2024/01/bombshell-inside-mrna-vaccines-a-human-molecule-diabolically-altered/
    BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy donshafi911 BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy January 6, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. In the cover image, the Canadian researcher Jessica Rose, author of an excellent biochemical analysis of an article from the University of Cambridge commenting a study by some of its researchers on the toxicity of manipulated human nucleoside in mRNA genetic sera by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell». With this phrase to be engraved in the history of the massive Covid vaccination campaign, the esteemed Canadian researcher, biochemist, immunologist and molecular biologist Jessica Rose (Source 1), author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridge in relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule” because it is a biological human component modified twice in the laboratory. (Source 1). UPDATE! Florida State Surgeon General Calls for Halt of mRNA Vaccines due to Dangerous, Oncogenes DNA Fragments Author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridgein relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule”because it is a biological human component modified twice in the laboratory. Billions of Dangerous Spike DNA’s Molecules inside Covid mRNA Vaccines. They can Reproduce the Toxic Protein in Human Cells for a Long Time This is the double alteration of Uridinetransformed into Pseudourine with the first synthetic biochemical alteration and then into N1-methylpseudouridine initialed “m1Ψ” as an acronym for N1-methyl-Ψ in which the Greek letter “Psi” was used to name Psueudoridine . Uridine is an organic compound, nucleoside,made up of the coupling of a molecule of ribose and one of uracil. Uracil is one of the two pyrimidine nitrogenous bases that form the nucleotides of RNA nucleic acid. This manipulation was designed by the Hungarian biochemist Katalin Karikó,awarded the 2023 Nobel Prize for Medicine precisely for having laid the foundations of mRNA vaccines, in order to “deceive” human cells into recognizing the synthetic mRNA as harmless human RNA … I apologize to the biochemistry experts for any transcription mistakes I may make trying to translate from a difficult chemical language the portentous scientific essence of the abundant technical quotations in the article published by Rose on her Substack, from which we will only extrapolate its introduction. Bombshell from US! FDA “Hides” Toxicity on DNA Fragments inside mRNA Vaccines despite Danger of Cancer Highlighted in its Guidance too Martin: “Pseudouridine Killer in the Vaccines for Depopulation” This analysis comes surprisingly providential as on Gospa News International we have just reported the summary of a conference by the famous patent expert David E. Martin in which he narrated in recent weeks the story of SARS-Cov-2 as a bacteriological weapon built in 58 years of military research on coronaviruses and that of mRNA vaccines, in his opinion, knowingly spread in a mass experiment for the search for vaccines against HIV-AIDS and cancer but also aimed at global depopulation. WUHAN-GATES – 73. Half of Century of Covert Bioweapon Development Leading to Fauci’s SARS-Cov-2 and to mRNA Lethal Vaccines In a very detailed article the American osteopath doctor Joseph Mercola wrote that «Martin points out that even if they don’t unleash any other bioweapons, the desired death toll may still be achieved, because they used pseudouridine in the mRNA shots, which is causing “turbo cancers”». Because: «Pseudouridine suppresses cancer-controlling agents and promotes oncogenic activity in the body, and this has been known since 2018, so its inclusion was hardly an accident. It’s a conspiracy, alright. But not a conspiracy theory in the dismissive sense. It’s a global conspiracy by identifiable agents who have, for nearly 60 years, plotted to commit, and profit from, the greatest genocide the world has ever seen, while hiding behind the false veneer of “public health.”». Well today, both the University of Cambridge and other authoritative scientists from around the world implicitly confirm that all those vaccinated with Covid mRNA with Moderna’s Spikevax and Pfizer-Biontech’s Comirnaty have been and continue to be unpaid and, above all, unaware human guinea pigs. Precisely because of this altered nucleoside… The Disturbing Article from Cambridge University The comment by the researcher Rose that we reported in the incipit of the article referred to the text of the University of Cambridge(Source 2) in relation to the study “N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting” by Mulroney et al.published on December 6, 2023 by Nature after more than a month of review. «Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses» is the eloquent title of the scientific text published by the British university. «The latest developments, led by biochemist Professor Anne Willis and immunologist Dr James Thaventhiran from the MRC Toxicology Unit at the University of Cambridge, build upon previous advances to ensure the prevention of any safety issues linked with future mRNA-based therapeutics. Their report is published today in the journal Nature» we read in the unsigned article. «The researchers identified that bases with a chemical modification called N1-methylpseudouridine – which are currently contained in mRNA therapies – are responsible for the ‘slips’ along the mRNA sequence» adds the university website. In collaboration with researchers at the Universities of Kent, Oxford and Liverpool, the MRC Toxicology Unit team«tested for evidence of the production of ‘off-target’ proteins in people who received the mRNA Pfizer vaccine against COVID-19. They found an unintended immune response occurred in one third of the 21 patients in the study who were vaccinated – but with no ill-effects, in keeping with the extensive safety data available on these COVID-19 vaccines». SCIENCE Magazine Finally Admitted the mRNA Vaccines Dangerous Side Effects! Shots linked to Long Covid, Neurologic Damages and POTS Despite disturbing the article already appears biased as it is aimed at “minimizing” the adverse reactions, even lethal one, that are accumulating in pharmacovigilance systems around the world, which have been confirmed by an alarming article in the journal Science, by the regulatory bodies from all over the world (EMA, FDA, etc.) and which led Moderna and Pfizer-Biontech to include the risk of lethal myocarditis in the information leaflets of their genetic drugs… 7 EURODEPUTATI CHIEDONO IL RITIRO DEI VACCINI COVID. Per Miocarditi Letali, Malori Improvvisi e Sicurezza Incerta nei Fragili British Study: “Incorrect mRNA Translation may Increase Toxicity” But it is the same authors of the study whose first signatory is Thomas E. Mulroney (Source 3), associate researcher of the Toxicology Unit of the MRC in Cambridge, who wrote the shocking considerations from a biochemical point of view in the conclusions. «We show that 1-methylΨ is a modified ribonucleotide that significantly increases +1 ribosomal frameshifting during mRNA translation and that cellular immunity to +1 frameshifted products can occur following vaccination with mRNA containing 1-methylΨ. To our knowledge, this is the first report that mRNA modification affects ribosomal frameshifting. Alongside this impact on host T cell immunity, the off-target effects of ribosomal frameshifting could include increased production of new B cell antigens». And they further add: «These findings are of particular importance to our fundamental understanding of how ribonucleotide modification affects mRNA translation, and for designing and optimizing future mRNA-based therapeutics to avoid mistranslation events that may decrease efficacy or increase toxicity». We will not delve further into the technical references but return to the analysis published by Jessica Rose in her Substack, making an extreme summary of it and advising professionals to read the text full of important images. Billions of DNA Fragments of Toxic Spike Protein and SV40 gene in the mRNA Vaccines. New Study: “They may Cause Turbo-Cancer” Let’s start with the comment added under the research published by Nature by her together with David Wiseman, L. Maria Gutschi, David J. Speicher, Kevin McKernan. Alongside the Canadian biologist they were already co-authors of the study “DNA fragments detected in the monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: exploratory dose-response relationship with serious adverse events” which induced the EMA to confess that Pfizer hid the use of the very dangerous SV40 gene in its vaccine, which can cause tumors. The same research encouraged the bioimmunologist Robert Malone to denounce the presence of the antibiotic resistance gene in the Moderna one, pointing out also that the pharmaceutical company was aware of the tumor risks of mRNA biotechnology as reported in its own patent. Bomba Mondiale! “NEI VACCINI COVID GENE DI RESISTENZA AGLI ANTIBIOTICI”. Studio Spagnolo lo Conferma. Ministro Schillaci lo CELA nell’Allarme Morti AMR We have written extensively about these topics in three investigations, one of which – on antibiotic resistance gene – is a world exclusive. Alarm of American Scientists for the New Research Let us therefore see the content of the comment by Rose and colleagues (Source 1)on Cambridge’s research: The paper provides evidence for the formation “off-target” or unintended proteins following vaccination with BNT162b2 due to frameshifting. Given the proposed mechanism, a similar problem is likely to exist for the Moderna product. While the authors have not isolated samples of these proteins from vaccinated patients or animals, their existence is evidenced by the specific cellular immune responses elicited to frameshifted proteins the authors synthesized. It is not clear why B cell – antibody responses were not studied. The authors state that “Although there is no evidence that frameshifted products in humans generated from BNT162b2 vaccination are associated with adverse outcomes.” BOMBSHELL: mRNA COVID jabs can Damage Children’s Immune Response to OTHER Viruses as well, Study finds It is unclear how it is possible to make this statement, given: • The small number of vaccinated subjects (n=21) providing samples. • This was not a controlled trial. • None of these subjects had reported undue effects of vaccination. Accordingly, the sample is subject to selection bias. • The toxicology of these unintended proteins must be studied. • The authors acknowledge the misdirected immunity “has huge potential to be harmful.” Translated into simpler words, no one has verified the selection methods of the samples which may have been chosen precisely because they did not have serious adverse reactions. SPIKE-DEMIC among Vaccinated: 83 % hit by PCVS Syndrome. Indian Study confirmed Gates, Big Pharma’s Health Disaster Furthermore, in the interests of expertise we read that the two Cambridge scientists Thomas E. Mulroney and Anne E. Willis «are inventors of a pending patent application (2305297.0) relating to mRNA technology» while in the information on the authors it is discovered that Alexander J Mentzer works at the Wellcome Center for Human Genetics, University of Oxford. Wellcome, with the Bill & Melinda Gates Foundation and the World Economic Forum, is among the founders of the Ngo CEPI(Coalition for Epidemic Preparedness Innovations) which has already launched the SKYCovion vaccine together with the London-based GSK, managed by CEO Emma Walmsley who is also director of Microsoft, and SK Bioscience. WUHAN-GATES – 73. BILL III A CACCIA DI CAVIE UMANE PER VACCINO COVID COREANO. “Genotossicità non Studiata” ma OMS & UK danno OK a SkyCovione con Spike Tossica e Adiuvante GSK da Pericoloso Squalene But let’s go back to the analysis made by Jessica Rose on the Cambridge researchers’ study: «The authors write that N1-methylpseudouridine affects the fidelity of mRNA translation via ribosome stalling that induces frameshifting. Frameshifting results in the production multiple, unique and potentially aberrant proteins». «The modified mRNAs for use in the COVID-19 products were codon-optimized for maximal protein expression in humans. Codon optimization, or synonymous codon replacement, rests on the idea that one can induce mutations throughout a gene of interest (like spike) based on an organism’s (like humans) codon usage bias, to increase translational efficiency and protein expression without altering the sequence of the protein. But, it is well-known that codon-optimization can lead to protein conformation, folding and stability problems». COVID: SCOPERTA LA PROTEINA CHE RIVELA I LETALI COAGULI DI SANGUE. Ma Nessuno Indaga sulla Correlazione coi Vaccini The Canadian immunologist further notes: «Codon optimization could affect protein conformation, folding and stability, change post-translational modification sites and even affect protein function.Different rates of translation by different tRNAs, including those that exhibit wobble base-pairing (a tRNA that can recognize multiple synonymous codons) may actually be critical for determining the rate of translation. The ribosome may slow and pause during elongation which may actually be necessary for proper protein folding. Therefore, codon optimization may disrupt the fine-tuned timing of translation and ultimately protein function». The Prophetic Seneff Study on Autoimmune and Neurocerebral Damage He then refers to other studies that had reported the dangers of this biochemical manipulation (Source 1): «Codon optimization can also lead to misfolding of mRNAs due to increased Guanine/Cytosine (GC content). Please read McKernan et al.’s preprint, Xia et al.’s paper and Seneff et al.’s paper to learn more about potential problems relating to codon optimization and GC content changes. The latter group write: Synonymous codon replacement also results in a change in the multifunctional regulatory and structural roles of resulting proteins». ONE in THREE Covid Vaccinated with Neurological Complications. Alarming Study from Italian National Research Council The risks to the human organism are clearly highlighted: «There is, in fact, a significant enrichment of GC content (17% and 25% enrichments as per Pfizer and Moderna, respectively, as compared to SARS-CoV-2) as a result of the codon optimization that was done, and this can lead to “dysregulation of the G4-RNA-protein binding system and a wide range of potential disease-associated cellular pathologies including suppression of innate immunity, neurodegeneration, and malignant transformation”. Increased GC content significantly alters mRNA secondary structure as well, and this can also lead to ribosomal pausing or stalling». These considerations were expressed in a study published by illustrious scientists such as Stephanie Seneff, Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA, USA, Greg Nigh, Immersion Health, Portland, OR, USA, Anthony M. Kyriakopoulos, Nasco AD Biotechnology Laboratory, Department of Research and Development, Piraeus, Greece and Peter A. McCullough, for Health Foundation, Tucson, AZ, USA, which was the subject of enormous censorship by specialized medical journals but we published in Gospa News thanks to an excellent summary by Dr. Mercola. Dangerous RNA Manipulation with N1-methyl-Ψ Below are the quotes from Seneff et al.(Source 4) useful for understanding the connection with uridine modified in N1-methyl-Ψ: «The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein». «However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance». The COVID Jabs’ Mechanisms of Injury: Sudden Death, Blood Cloths, Human Mad Cow and Autoimmune Diseases In the study entitled “Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs” the scientists added: «These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health». The late biologist Luc Montagnier, in a study published posthumously by his research friends Jean-Claude Perez and Claire Moret-Chalmin with a review contribution from Seneff biophysics, proved without a shadow of a doubt the correlation between killer prions caused by vaccines and rapid deaths for neurocerebral Creutzfeldt-Jacob disease, human mad cow disease. PRIONS as KILLERS: 25 Deaths due to a New Mad-Cow from Covid Vaccines. Shocking Research by Montagnier (RIP), Perez & Moret-Chalmin on CJD Brain Damages In detail Seneff and the other scientists also refer to specific alterations: «Impaired type I IFN signaling is linked to many disease risks, most notably cancer, as type I IFN signaling suppresses proliferation of both viruses and cancer cells by arresting the cell cycle, in part through upregulation of p53, a tumor suppressor gene, and various cyclin- dependent kinase inhibitors (Musella et al., 2017; Matsuoka et al., 1998). IFNα also induces major histocompatibility (MHC) class 1 antigen presentation by tumor cells, causing them to be more readily recognized by the cancer surveillance system (Heise et al., 2016)». They then delve into the problem of the uridine molecule. To understand its importance we report a note from Rose: «Pseudouridines (Ψs) are a normal and essential part of our biology. They have been called the 5th nucleotide, in fact, and “are a ubiquitous constituent of structural RNA (transfer, ribosomal, small nuclear (snRNA) and small nucleolar), and present in coding RNA, across the three phylogenetic domains of life”and “accounts for about 1.4% of all bases in human rRNAs”». “mRNA COVID-19 Vaccines are Like Gene Therapy Products” French Study highlighted Omitted Controls on Genotoxicity Here’s what Seneff and his colleagues wrote about vaccines: «A breakthrough came when it was discovered experimentally that the mRNA coding for the spike protein could be modified in specific ways that would essentially fool the human cells into recognizing it as harmless human RNA. A seminal paper by Karikó et al. (2005) demonstrated through a series of in vitro experiments that a simple modification to the mRNA such that all uridines were replaced with pseudouridine could dramatically reduce innate immune activation against exogenous mRNA». Cancer Risk pointed out by the Nobel Inventor of mRNA Vaccines Precisely for this discovery, Hungarian researcher Katalin Karikó, long-time at Biontech, recently received the Nobel Prize for Medicine together with her American colleague Drew Weissman, although both warned of the dangers of the new mRNA biotechnology. Medicine Nobel to mRNA Covid Vaccines’ Scientists, both Sponsored by Gates, Fauci and Zuckerberg In particular, on January 6, Karikó declared to the German newspaper Welt (Source 5): «Every day I receive many emails from people who write to me about their experiences. One woman wrote to me that two days after the vaccination she developed a large lump in her breast. Vaccination caused cancer, it was her conclusion. But the cancer was already there, only vaccination gave an extra boost to the immune system, so that the immune defense cells rushed in large numbers towards the enemy». The Gospa News investigations on Turbo-Cancer based now on seven published scientific studies have highlighted a very strong correlation between mRNA gene sera and the appearance or reactivation of tumor phenomena with abnormal degeneration resulting in lethal outcomes. TURBO-CANCER – 2. Many Lethal/Serious Cases and New Researches on Covid mRNA Vaccines Risks. Melatonin Hope… Karikó herself adds: «Vaccination provides a strong boost to the immune system. It can happen that a dormant infection breaks out in people with an already weakened immune system. The extent to which this is the case for shingles will need to be examined more closely». Gospa News did so by discovering 27 thousand cases of Herpes Zoster, in the European Union only, as adverse reactions to vaccines reported by EMA pharmacovigilance database even in children, who are more exposed to damage to the natural immune system as confirmed by recent research. Esclusivo! EPIDEMIA DI HERPES DOPO I VACCINI COVID. 27mila Casi nell’UE: 31 Morti da Zoster. Lo Studio: “Per danni al Sistema Immunitario” Let’s go back to Seneff’s conclusions: «Andries et al. (2015) later discovered that 1-methylpseudouridine as a replacement for uridine was even more effective than pseudouridine and could essentially abolish the TLR response to the mRNA, preventing the activation of blood-derived dendritic cells. This modification is applied in both the mRNA vaccines on the market (Park et al., 2021)». To put it simply, the dendritic cell plays the role of sentinel and if it senses the presence of a pathogen in the body, it stimulates the immune response of B and T lymphocytes, specific against that antigen. If its action is limited or suppressed, it may become incapable of dealing with viral or bacterial enemies but also tumor dangers. Critical Role of Pseudouridine in mRNA Vaccines A study published by Pedro Morais, Director (Pseudouridylation Technology) ProQR Therapeutics, Leiden, Netherlands, and by Department of Biochemistry and Biophysics, Center for RNA Biology, University of Rochester Medical Center, Rochester, NY, US, entitled “The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines” highlighted the fundamental role of the laboratory alteration of this protein in the Comirnaty and Spikevax genetic sera (source 6). «Both consisted of N1-methyl-pseudouridine-modified mRNA encoding the SARS-COVID-19 Spike protein and were delivered with a lipid nanoparticle (LNP) formulation. Because the delivery problem of ribonucleic acids had been known for decades, the success of LNPs was quickly hailed by many as the unsung hero of COVID-19 mRNA vaccines». “European Medicines Agency Knew Toxicity of Pfizer Covid Vaccine”. Bombshell Study Published in US by an Italian BioChemist on Dangers mRNA-LNPs But the scholars, one of whom has a clear conflict of interest because he is director of the Pseudouridylation Technology project, have highlighted another very interesting fact: «However, the clinical trial efficacy results of the Curevac mRNA vaccine (CVnCoV) suggested that the delivery system was not the only key to the success. CVnCoV consisted of an unmodified mRNA (encoding the same spike protein as Moderna and Pfizer-BioNTech’s mRNA vaccines) and was formulated with the same LNP as Pfizer-BioNTech’s vaccine (Acuitas ALC-0315).However, its efficacy was only 48%. This striking difference in efficacy could be attributed to the presence of a critical RNA modification (N1-methyl-pseudouridine) in the Pfizer-BioNTech and Moderna’s mRNA vaccines (but not in CVnCoV)». “Toxic Nanoforms inside Pfizer-Biontech Covid Vaccine”. Vital Study by Italian Biochemist on US Journal of Virology highlights an Alleged Crime However, the same researchers highlight a significant note: «The intrinsic immunogenicity of non-modified mRNA was once considered a potential advantage for its use in vaccines(Ishii and Akira, 2005) as it would encode the antigen and concomitantly serve as an adjuvant while permitting a low dose. In fact, the unmodified COVID-19 mRNA vaccine candidate in late-stage clinical trials (CVnCoV, developed by Curevac) had a maximum dose of 12 µg». Curevac was developed by Curevac NV of Tubingen, together with the Ngo CEPI founded by Bill Gates with Wellcome and WEF, which initiated an authorization process before the CHMP committee of the European Medicines Agency (EMA) but withdrew it due to its low efficacy on October 12, 2021 (source 7) in view of the arrival of a new pharmacological product developed with GSK financed by Gates himself. MINISTRO SCHILLACI SPECULA SU BIG PHARMA FINANZIATA DA GATES. €700mila Investiti in Biomediche USA che Testano anche Vaccini DNA Covid Here is another cryptic phrase in which we talk about the “safety” of vaccines, implicitly implying that it is not clear in the current vaccines which therefore make all those who take them into “human guinea pigs”from the laboratory as the immunologist Rose clearly highlights in her final bioethical considerations. Rose: “Unpredictable Health Effects of Manipulated Codons” «Ehden Biber also wrote a great article about the pitfalls of codon optimization that you can read here. In a Nature article published in 2011 entitled: “Breaking the silence”, the author writes on the potential danger of fiddling with codons in therapeutic proteins whereby it “could have unpredictable effects on people’s health”» Rose wrote in her comment on the Cambridge research quoting many sentences by scientific journalist Alla Katsnelson which we report below. Bombshell! Texas Attorney General sues Pfizer on Covid Vaccine Efficacy and Conspiring In detail, the Canadian researcher adds: «She points to a study where the authors show that a synonymous codon change found in the most common form of cystic fibrosis results in mRNA misfolding. (Keep this in mind.) She also points out that in the context of the multi-drug resistance 1 gene (MDR1) (the gene that encodes P-glycoprotein), that a codon change may interfere with the pauses that characterize RNA passing through the ribosome, thereby changing how the growing amino acid chain folds». «But perhaps the most timely and spine-tingly relevant statement in this article is found at the end, and I quote: “At the moment, companies developing recombinant therapies must verify that the DNA sequence designed by their scientists is the one that’s producing their proteins, but they aren’t required to note how different that is from the native genetic code”». European Regulator: Pfizer Hid Dangerous Cancer Gene! It Kept Secret the SV40 DNA Sequence In COVID-19 Vaccine We do not have any guidance with regard to the [DNA] sequence,” Kimchi-Sarfaty notes. While it was the Italian bioimmunologist Mauro Mantovani who demonstrated how the “double Proline” inserted in mRNA vaccines makes the toxic Spike protein dangerously persistent in the human body. «That’s one piece of data that could be tracked by the system she is proposing. Such knowledge, in turn, could ultimately help define better strategies for optimization and possibly even make biologic drugs safer for people» adds Alla Katsnelson while the immunologist asks herself a question: «I wonder if the FDA ever took her advice to track the differences in codons and the resulting potential adverse effects?» Covid Vaccines Killer Pathologies in a Name Only: Spikeopathy! Huge, Chilling Study on mRNA Genic Serums’ Serious Adverse Reactions Therefore Rose quoted the article which we analyzed before: «In addition to our comment on the Nature paper, a University of Cambridge write-up entitled: Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses was penned. They make it clear that the most relevant conclusion from the Nature paper is that we can make more products similarly insanely dangerous as the ones pumped into billions of bodies because we can simply ‘reduce the production of frameshifted products’ by ‘synonymous targeting of slippery sequences’». So she wrote her milestone sentence: «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell». Moderna AWARE that mRNA Jabs cause CANCER due to DNA Fragments. Malone Unveils Patent The Canadian molecular biologist concludes before going into detail about a biochemical analysis that is too technical for non-experts: «The manufacturers might have thought to explore options to prevent potentially harmful responses from their products prior to injecting billions of people with them. It is criminal that these products continue to be forced onto newborns and infants by mandate, to this day». And then she report an emblematic quote about the risks of “Fooling with Mother Nature” by an evolutionary cell biologist at the University of Chicago: “Please do not monkey with these sites; they are optimized for some reason”, in reference to codon bias in mammals. Fabio Giuseppe Carlo Carisio © COPYRIGHT GOSPA NEWS prohibition of reproduction without authorization follow Fabio Carisio Gospa News director on Twitter follow Gospa News on Telegram MAIN SOURCES SOURCE 1 – JESSICA ROSE – That Substack about N1-methylpseudouridines and frameshifting SOURCE 2 – UNIVERSITY OF CAMBRIDGE – Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses SOURCE 3 – NATURE – N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting SOURCE 4– PUBMED – Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs SOURCE 5 – WELT – “Das ist der wirkliche Grund, warum man unter neuen Varianten nicht mehr so krank wird“ SOURCE 6 – FRONTIERS IN – The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines SOURCE 7 – EMA ends rolling review of CVnCoV COVID-19 vaccine following withdrawal by CureVac AG Fabio G. C. Carisio Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal. His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more… Most popolar investigation on VT is: Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting. For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime. With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians. In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence. In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates His investigations was quoted also by The Gateway Pundit, Tasnim and others He worked for many years for the magazine Art & Wine as an art critic and curator. VETERANS TODAY OLD POSTS www.gospanews.net/ ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/01/bombshell-inside-mrna-vaccines-a-human-molecule-diabolically-altered/
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    BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered
    In the cover image, the Canadian researcher Jessica Rose, author of an excellent biochemical analysis of an article from the University of Cambridge commenting a study by some of its researchers on the toxicity of manipulated human nucleoside in mRNA genetic sera by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO «Well of course! Now that we know that...
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