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

The emergence of nanobot society OUTRAGED HUMAN So, they injected it into the military, police, emergency services.... Now everyone is injected with a device with a "real IP ADDRESS".... 0:00 Thank you very much. So one word of notice before we begin, 0:03 all the technologies that you are going to see here now are real. 0:06 And with that said 0:07 I'd like to first tell you the story about 0:10 this uh... little girl named Dana 0:12 she's very special for me because she's my daugther 0:14 and Dana was born with a leg condition requiring frequent surgeries like this one 0:19 uh... she had when we were in Boston 0:21 and um... I remember taking her to that particular surgery 0:25 and uh... 0:26 I rembember her being admitted and she was excited at first 0:31 and then just before they got into her the OR 0:33 I looked at her and she was... afraid, she was little worried and 0:38 who wouldn't be? Because surgeries today are complicated 0:41 and they're often very risky. 0:42 Now let's imagine a few years into the future, into the near future hopefully, 0:47 Dana will arrive to hospital for her ??? surgery 0:50 and instead of being prepped for anesthesia for the OR 0:54 the surgeon will just take a syringe and inside the syringe 0:58 there are millions of tiny robots, of tiny machines 1:02 that will be injected into Dana's bloodstream. 1:04 They will autonomously locate the place they need to be in, 1:08 they will excite out the injured tissue, 1:11 then will remove dead cells, 1:13 then they will... 1:14 stimulate and guide the regrowth of healthy cells across those tissue gaps, 1:18 they will release drugs that relief pain and reduce inflammation 1:23 and all the while Dana will be sitting on the chair 1:25 eating a sandwich, reading a book, might be the next 1:28 twilight saga book which she'll be able to read because she will be 16 by then 1:32 And...(giggles) 1:33 uh... when these robots 1:35 have completed their job they'll simply disintegrate 1:39 and disappear from her bloodstream the next day. 1:42 So these nanobots have been envisioned in the past 30 years 1:45 by people like Eric Drexler, Robert Freitas and Ray Kuzweil. 1:49 Today I'm going to show you that these robots exist 1:51 here in Israel. 1:54 I'll show you this syringe 1:56 which I've brought from my lab. 1:58 So this syringe has inside it a thousand billion robots. 2:03 So these robots are each fifty nanometers 2:06 long as you can see in this slide under the microscope. 2:11 Fifty nanometers is about 2000 times thinner than the thickness of your hair 2:16 OK? And... umm... These robots were born actually 3 years ago 2:20 in a research I did with Shawn Douglas, now a UCSF Professor. 2:24 But over the past year and a half 2:25 in my group at Bar-Ilan University 2:27 We've been developing and testing robots for a variety of 2:31 medical and therapeutic tasks. 2:33 We've invented ways of making them safe for use 2:37 and non-inmunogenic 2:38 and we learned how to tune their stability in our bloodstream 2:41 to fit either short-term or long-term 2:44 even days long medical procedures. 2:47 So to carry out medical and therapeutic procedures in our body 2:50 with the upmost precision, 2:51 we need to be able to control molecules 2:53 Controlling molecules is a very simple challenge 2:56 in modern scientific knowledge. 2:58 OK? Let's speak for example about the class of molecules we know as drugs 3:02 So despite... 3:04 amazing progress made in the past four decades 3:06 the way we think about drugs and we the way we use drugs 3:09 has been essentially unchanged 3:11 and it's similar as two hundred years ago 3:14 right? You hear about about big pharmaceutical companies 3:17 spending huge amounts of money 3:19 searching for better, safer drugs. 3:22 Attempts that usually fail. 3:24 OK? but, 3:25 searching for let's say a safer cancer drug, 3:28 half it is a concept that has a flaw in it. 3:30 Because searching for a safer cancer drug 3:32 is basically like searching for a gun that kills only bad people 3:36 We don't search for such guns, 3:37 what we do is training soldiers to use that gun properly 3:42 Of course in drugs we can't do this because it seems very hard 3:45 But there are things we can do with drugs 3:47 for example, we can put the drugs 3:49 in particles from which they difuse slowly. 3:51 We can attach a drug to a carrier 3:54 which takes someplace but, this is not real control. 3:57 When we were thinking about control we're thinking about 4:00 processes is the real world around us 4:02 and what happens when we want to control a process 4:06 that's beyond our capabilities as humans 4:08 we just connect this process to a computer 4:10 and let the computer control this process for us. 4:13 OK? So that's what we do. 4:15 But obviously this cannot be done with drugs because 4:19 the drugs are so much smaller than the computers as we know them 4:23 The computer is in fact so much bigger 4:25 it's about a hundred million times bigger that any drug molecule. 4:28 Our nanobots which were in the syringe 4:31 solve this problem because they are in fact 4:34 computers the size of molecules. 4:36 and they can interact with molecules 4:38 and they can control molecules directly, 4:40 so just think about all those 4:42 drugs that have been withdrawn from the market 4:45 for excessive toxicity 4:46 right? 4:47 It doesn't mean that they are not effective, 4:49 they were amazingly effective, 4:51 they were just guns shooting in all directions 4:53 but in the hands of a well-trained soldier 4:56 or a well-programed nanobot 4:58 using all the existing drugs 5:01 we could hypothetically kill almost any disease. 5:05 So we might not need even new drugs. 5:07 We have amazing drugs already, 5:09 we just don't know how to control them, this is the problem 5:11 and our nanobots... 5:13 hopefully solve this problem and I'll show you how. 5:15 So there is an interesting question "how do we build 5:19 a robot or a machine the size of a molecule?" 5:21 so the simple answer would be: we can use molecules 5:25 to build this machine. 5:26 So we're using molecules, but we're not using just any molecule. 5:30 We're using the perfect, most beautiful molecule on earth, at least in my opinion, 5:34 which is DNA. 5:36 And in fact every part of the robot, 5:38 every part of out nanorobots: 5:40 Moving parts, axis, locks, chasis, software, 5:44 everything is made from DNA molecules. 5:46 And the techonology that enables us to do this 5:49 originated thirty years ago when the pioneering works of Nadrian Seeman, 5:52 culminating 7 years ago in the works of Paul Rothemund from Caltech, 5:56 which was also featured in TED, 5:58 and it's called DNA origami. 5:59 Now in DNA origami we do not use a piece of paper, 6:02 we use a single long strand of DNA 6:05 and we fold it into virtually any shape we want. 6:08 For example these shapes, so these are actual microscopic images 6:12 of shapes the size of molecules that were folded from DNA. 6:16 so the smiley you see here in the center of the screen for example 6:19 are a hundred nanometers in size 6:21 and we make billions of them in few... in a single reaction. 6:24 Now since 2006 several researchers, really talented ones, 6:28 have been expanding the limits of the technically feasible in DNA origami 6:32 and now we have an astonishig array of shapes and objects which we can build 6:35 using this technique. 6:36 And these researchers also gave us computer-aided design tools 6:41 that enable everyone 6:43 very very simply to design objects from DNA 6:46 So these CAD tools amazingly 6:49 enable us to focus o n the shape we want 6:52 forgetting the fact that these structures are in fact assemblies of molecules. 6:57 so this is for example a shape the computer can actually turn into DNA molecules. 7:02 and the output of this CAD software, as you can see, 7:05 is a spreadsheet with fragments of DNA 7:08 which you can attach to a message and send to a company 7:11 one of two dozen companies that make DNA by order and you'll get those DNA's 7:16 several days later to your doorstep 7:18 and when you get them all you need to do is just mix them in a certain way 7:23 and these molecular bricks will self-assemble into 7:26 millions of copies of the very structure that you designed using that CAD software 7:30 which is free by the way, you can download it for free. 7:34 So, let's have a look at our nanorobots. 7:38 So, this is how the nanorobots look like, it's built from DNA as you can see 7:42 And it resembles a clam shell in which you can put cargo 7:45 You can load anything you want starting from small molecules, drugs, 7:49 proteines, enzymes, even nano-particles. Virtually any function 7:54 that molecules can carry out, can be loaded into the nanobot 7:57 and the nanobot can be programmed to turn on and off 8:01 these functions at certain places and at certain times 8:05 this is how we control those molecules 8:07 and so this particular nanorobot is in an off state, it's closed,it's securely 8:12 sequestres anything, any payload you put inside 8:16 so it's not accessible to the outside of the robot, 8:18 for example, it cannot engage target cells or target tissues 8:22 But we can program the nanobot to switch to an on state 8:26 based on molecular cues it finds from the environment 8:30 so programming the robot is virtually like assemblying a combination lock 8:34 using disks that recognize digits, 8:37 but of course instead of digits we are assemblying disks that recognize molecules. 8:42 So these robots can turn from off to on and when they do 8:47 any cargo inside is now accessible, 8:49 it can attack target cells or target tissues 8:52 or other robots which you'll see later on. 8:54 And so we have robots that can switch from off to on 8:58 and off again, we can control their kinetics of transition. 9:02 We can control which payload becomes accessible at which time point 9:05 Let's see an example how these robots for example control a cancer drug 9:12 So what you can do is you can take nanobots, 9:14 you can put the nastiest cancer drug you may find 9:17 into the robots, even a cancer drug 9:19 that's been withdrawn because of excessive toxicity 9:23 Ok? When the robot is locked 9:25 and you put them in your mixture of healthy cells and tumor cells 9:29 nothing happens, no cell is affected, because the robot 9:32 safely sequesters those drugs inside. 9:35 When we unlock the robots 9:37 all cells die because the cargo inside the [robot] attacks anything on sight. 9:42 So all cells eventually die. In this case this is a fluorescent molecule 9:46 to help us see better the output. 9:48 But when we program the nanobots to search for tumor cells particulary, 9:53 so only the tumor cells 9:56 uh... only the tumor cells die because 9:59 the robot doesn't care about the bystander cells, about the healthy cells. 10:04 So it does not harm them at all. 10:06 And we have nanorobots in our lab that can target 10:09 about ten types of cancer already and other cell targets 10:12 and my team keeps expanding this range monthly. 10:17 So these are nanorobots and to another topic 10:22 organisms in nature, like bacteria and animals 10:26 have learned very early in evolution that working in a coordinated group 10:29 conveys advantage 10:31 and capabilities beyond those of the individual 10:34 and since we are interested in 10:36 very complex medical procedures, very complex therapeutic settings, 10:40 we're wondering what we could do 10:42 if we could engineer artificial swarm behaviors 10:46 into our nanobots as well so we could have extraordinarily large groups of nanobots 10:51 Can we teach them to behave like animals, like insects 10:55 and how do you do this? So the question is interesting. 10:58 So you could think one way to do it would be 11:01 to look at a natural swarm like this one of fish 11:04 and simulate the dynamics of the entire swarm and then try to write the codes 11:09 in molecules of course 11:10 that mimic the same behaviour 11:12 this is virtually impossible, it's impractical 11:15 what we do is we take the single fish or a single nanobot in our case 11:20 and you design a very basic set of interaction rules 11:23 and then you take this one, this nanobot, you make a billion copies of it 11:27 and you let the behaviours emerge from that group 11:31 let me show you some examples of the things we can already do 11:35 for example, just as ants 11:38 can shake hands and form physical bridges between two trees 11:42 or two remote parts of the same tree, 11:44 we already have nanorobots that can reach out for each other 11:47 touch each other and shake hands in such a way 11:49 they form physical bridges. 11:51 Then you can imagine these robots 11:53 extending, making bridges extending from one-half 11:56 to the other half of an injured tissue, 11:58 an injured spinal cord for example 12:00 or an injured leg in the case of Dana, my daughter 12:03 and once they stretched over that tissue gap 12:06 they can apply growth factors, as payloads, and those growth factors 12:10 stimulate the re-growth and guide re-growth of cells across the gap. 12:14 So we already did that and... 12:17 we have robots that can cross regulate each other just like animals do in groups 12:21 and this is amazing because as you can see here 12:24 you can have two types of robots, Type-A and Type-B 12:28 they can cross regulate each other, such that "A" is active 12:32 while "B" is not and viceversa. 12:34 So this is good for combination therapy 12:36 with combination therapy we take multiple drugs, right? 12:39 and sometimes two or more of these drugs 12:41 can collide and generate side effects, 12:43 but here you can put one drug here, one drug here 12:46 and the robots will time the activities so that 12:49 one drug is active, the other is not and then they can switch 12:52 and so two or more drugs can operate at the same time without actually colliding. 12:57 Another example that we did is the quorum sensing. 13:00 Now quorum sensing is great, it's a bacterial inspired behaviour 13:05 It means nanorobots can count themselves 13:08 and they can switch to "on" only when reaching a certain population size 13:12 this is a mechanism invented by bacteria in evolution 13:15 and they regulate amazing behaviours based on just their population density 13:18 for example, bioluminescence, this one of the well-studied examples 13:23 so our robots can count themselves and switch to on 13:26 only when reaching a certain population size which we can program. 13:29 This is great because this is a mechanism of programming a drug 13:33 to become active only when reaching a certain dose 13:36 around the target, regardless of its inherent dose-response curve. 13:41 One last I'm gonna show to you is computing, 13:43 so this nanobots can do computing. 13:45 How's so? If you think about your computer at home, 13:48 the processor of the computer is in fact a gigantic swarm of transistors 13:53 In an i7 core for example you have 800 million transistors approximately 13:58 and they're set to interact in certain ways to produce logic gates 14:02 and these logic gates are set to interact to produce computations 14:05 so we can also produce computation by setting interactions between nanorobots 14:10 to emulate logic gates like you see here 14:13 and they form chains and they form pairs 14:15 and my team in Bar-Ilan University [has] already developed several architectures 14:19 of computing based on interacting nanorobots 14:22 and to prototype these 14:24 we are using animals, very interesting animals 14:27 these are cockroaches, 14:28 they are very easy to work with, the're very sweet, 14:30 they're actually from South America 14:32 and I'm a Soutamerican myself so I fell kinda related 14:35 [Laughter] 14:36 And hum... so what we do is we inject those robots into the cockroach 14:40 and to do that we of course had to put the cockroaches to sleep 14:43 have you ever tried putting cockroach to sleep? 14:46 We put in the freezer for seven minutes 14:48 in they fall asleep 14:49 and we can inject these nanorobots inside 14:52 and after 20 minutes they start running around, they're happy. 14:55 And those robots 14:57 while they're doing this, the robots read molecules 14:59 from the cockroaches' inputs 15:01 and they write their outputs in the form of drugs 15:04 activated on those cockroaches' cells 15:06 so we can do, we can see that and we already have, as you can see, 15:09 architectures of interecting nanorobots that can emulate logical operators 15:14 and you can use these as modular parts to build any type universal computer you want 15:19 [....] 15:21 that can control multiple drugs simultaneously 15:25 as a result of biocomputing, this is real universal computing in a living animal. 15:30 Now we already have systems that have [the] computing capacity 15:33 of an 8-bit computer like Commodore 64. 15:36 To make sure we don't lose control over the nanobots after they're injected 15:40 my team [has] developed nanorobots that carry antennae 15:44 these antennae are made from metal nano-particles. 15:47 Now, the antennae enable the nanobots 15:49 to respond to externally applied electromagnetic fields 15:52 so these nanorobots, this version of nanobots 15:55 can actually be activated with a press of a button on a joystick 15:58 or for example using a controller 16:01 such as the Xbox or Wii if you ever had the chance of playing with those 16:05 and you can see one of my students in the lab configuring an Xbox app 16:09 to control nanobots. 16:11 For example you can imagine nanorobots being injected 16:14 to Dana, my daughter for example, 16:16 and the doctor can guide those robots 16:19 into the site, into the leg and just activate them with a hand gesture. 16:23 And you can already see an example where we actually took 16:26 cancer cells and loaded robots with cancer drugs 16:29 and activated the drug by a hand gesture. 16:31 and we can actually kill cancer cells just by doing this, 16:34 as you can see here. 16:36 And the interesting thing is that 16:39 because the controller like the Xbox is connected to the internet, 16:44 the controller actually links those nanobots to the network 16:47 so they have an actual IP address 16:49 and they can be accessed from a remote device sitting on the same network, 16:53 for example, my doctor's smartphone 16:55 So, OK?, just like controlling a controller, this can be done. 17:00 The last thing I'm gonna show is, if you look at our body 17:04 you'll see that every cell type, every organ, every tissue 17:08 has their own unique molecular signature 17:11 and this is equivalent to a physical IP address made of molecules 17:15 and if you know these molecules 17:17 you can use those nanobots to browse the Organism Wide Web, as we call it 17:21 and you can program them to look for bits, 17:23 this could be for example signally molecules between cells, 17:26 and either fetch them for diagnostics 17:28 or carry them to different addresses. 17:30 And we already have robots that can hijack 17:33 signals between cells 17:34 and manipulate an entire network of communications between cells 17:37 and this is great for controlling very complex diseases in which many cell types 17:43 communicate and orchestrate to perpetuate a disease. 17:46 So before I finish I'd just like to thank 17:50 my amazing team at Bar-Ilan University 17:52 and all the colleagues that took part in this extraordinary journey, 17:55 starting from the George Chuch's Lab in Harvard 17:57 and ending today in Bar-Ilan University in the new Faculty of Life Sciences, 18:01 and I really hope that 18:03 anywhere between a year and five years from now 18:06 we'll be able to use this in humans 18:08 and finally witness the emergence of nanobot society. 18:11 Thank you very much. https://www.digitaltrends.com/cool-tech/nanobots-live-cockroach-thought-control/ https://www.digitaltrends.com/cool-tech/nanobots-live-cockroach-thought-control/ https://www.timesofisrael.com/israeli-scientists-use-nanobots-and-thoughts-to-administer-drugs/ Israeli scientists say they have come up with a way for brain power to control when drugs are released into the body, by using tiny robots made out of DNA to deliver the medication internally. Researchers at the Interdisciplinary Center in Herzliya and Bar-Ilan University in Ramat Gan have built the nanobots to which medication is attached and then are injected into the body. The nanobots have a “gate” that opens or closes — thereby controlling drug release — depending on brain activity. In order to achieve this, the New Scientist magazine said, the researchers developed a computer algorithm that could tell whether a person’s brain was resting or carrying out some form of mental activity, such as math problems. A fluorescent-tinted drug was then added to the nanobots, which were injected into a cockroach placed inside an electromagnetic coil. Israeli scientists say they have come up with a way for brain power to control when drugs are released into the body, by using tiny robots made out of DNA to deliver the medication internally. This coil was then connected to an EEG cap worn by a person asked to perform mental calculations. The computer recognized increased brain activity by the cap wearer, which triggered the “gate” on the nanobots inside the cockroach, releasing the fluorescent drug that was visible as it spread through the insect’s body. The idea is to use the delivery system for people with mental health issues, which are sometimes triggered before sufferers are aware they need medication. By monitoring brain activity, the nanobots could deliver the required preventative drugs automatically, for example before a violent episode of schizophrenia. https://www.newscientist.com/article/2102463-mind-controlled-nanobots-could-release-drugs-inside-your-brain/ The group has built nanorobots out of DNA, forming shell-like shapes that drugs can be tethered to. The bots also have a gate, which has a lock made from iron oxide nanoparticles. The lock opens when heated using electromagnetic energy, exposing the drug to the environment. Because the drug remains tethered to the DNA parcel, a body’s exposure to the drug can be controlled by closing and opening the gate. By examining when fluorescence appeared inside different cockroaches, the team confirmed that this worked. The idea would be to automatically trigger the release of a drug when it is needed. For example, some people don’t always know when they need medication – before a violent episode of schizophrenia, for instance. If an EEG could detect it was coming, it could stimulate the release of a preventative drug. https://www.youtube.com/watch?v=BxJPceCV51g Nanobots Successfully Used on Living Animal for the First Time - IGN News 0:38 to treat human ailments or weaponized 0:40 hijacked by a snake themed terrorist 0:42 organization and then used to destroy 0:43 Paris but I suppose it's only a matter 0:45 of time “This syringe has inside it a thousand billion robots.” https://outraged.substack.com/p/the-emergence-of-nanobot-society?utm_source=cross-post&publication_id=1087020&post_id=143145132&utm_campaign=956088&isFreemail=true&r=1sq9d8&triedRedirect=true&utm_medium=email Follow @zeeemedia Website | X | Instagram | Rumble https://donshafi911.blogspot.com/2024/04/the-emergence-of-nanobot-society.html

COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers. COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher (CROCOTHERY/Shutterstock) Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA. The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed. These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times. DNA Integration Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome. Story continues below advertisement “Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA. Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research. Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines. Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA. Story continues below advertisement After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk. However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear. Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory. Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said. Story continues below advertisement “The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times. Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results. The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients. Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells. Story continues below advertisement However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data. His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12. “A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said. Not Random Events The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12. Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random. Story continues below advertisement “There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA. Highly activated DNA tends to play important roles in the human body. The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change. Vaccine DNA Is Active in the Cells Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times. Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA. Story continues below advertisement These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells. Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors. What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said. DNA Contamination From mRNA Vaccine Manufacturing DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process. This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency. The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance. Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA. However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine. In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination. However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this. Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose. Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells. https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184

Scientist claims ‘smoking gun’ evidence COVID-19 intentionally created by researchers in Chinese lab Ronny Reyes COVID-19 may have been created in a Chinese lab, a British professor told the UN Wednesday, with another expert claiming that evidence of the likelihood has reached “the level of a smoking gun.” Richard H. Ebright, a molecular biologist at Rutgers University, was quoted saying in a new Wall Street Journal article that the virus that killed millions around the world may actually have been manmade in China’s Wuhan Institute of Virology. He cited evidence found in a 2018 document from the lab that talked of making such a virus. Advertisement “[The document] elevates the evidence provided by the genome sequence from the level of noteworthy to the level of a smoking gun,” Ebright said in the piece by former New York Times editor Nicholas Wade. Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was man-made. 4 Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was manmade. Rutgers New Brunswick The papers from the lab cited by Ebright contained drafts and notes regarding a grant proposal called Project DEFUSE, which sought to test engineering bat coronaviruses in a way that would make them more easily transmissible to humans. The proposal was ultimately rejected and denied funding by the US Defense Advanced Research Projects Agency, but Wade suggested that their work could have been carried out by researchers in Wuhan who had secured Chinese government funding. Advertisement “Viruses made according to the DEFUSE protocol could have been available by the time Covid-19 broke out, sometime between August and November 2019,” wrote Wade, a former science editor of the New York Times. Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. 4 Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. AFP via Getty Images “This would account for the otherwise unexplained timing of the pandemic along with its place of origin.” Along with the research notes, Wade claimed the specific genetic structure of the coronavirus that allowed it to infect humans served as another strong indication of “the virus’s laboratory birth.” Advertisement “Whereas most viruses require repeated tries to switch from an animal host to people, SARS-CoV-2 infected humans out of the box, as if it had been preadapted while growing in the humanized mice called for in the DEFUSE protocol,” Wade wrote. While scientists continue to debate whether the coronavirus pandemic was a natural occurrence or manmade, Ebright believed there was credibility that the work proposed by the now-controversial EcoHealth Alliance led to the development COVID-19. Following the release of the 2018 documents — which were published by US Right to Know through a Freedom of Information Act request — Ebright said there was clearer evidence that the virus was manufactured in a lab, the Daily Telegraph reported. Advertisement The 2018 documents contained drafts and notes regarding Project DEFUSE and how to synthesize bat coronaviruses to make them more transmissible. The Wuhan Institute of Virology stands at the center of scrutiny over the origins of Covid-19. 4 The Wuhan Institute of Virology stands at the center of scrutiny over the origins of COVID-19. AFP via Getty Images The researchers proposed introducing “appropriate human-specific cleavage sites” to the spike proteins of SARS-related viruses in the lab, the same method several biologists have said could have been used to synthesize the coronavirus that led to the pandemic. According to the documents, the researchers had planned to conduct a portion of the research at the Wuhan lab where they noted that safety conditions were not up to US standards, to the point where they claimed American scientists would “likely freak out.” Advertisement A spokesperson for EcoHealth Alliance said its research played no role in the start of the COVID-19 pandemic. “Documents representing incomplete or early drafts of the proposal have been acquired via the Freedom of Information Act and published along with allegations regarding their intent. These allegations are false, based on misunderstanding of edits and comments on the document, and based on misleading out-of-context quotations, and a lack of understanding of the process by which federal grants are awarded,” the spokesperson said. “Because the work was not selected for funding, any assertions about these details are by definition based on review of incomplete information and are extremely misleading.” Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London. 4 Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, called on scientists to follow more rigorous safety standards. King College London Advertisement While COVID-19’s origins remain a mystery, Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, said the world needed to acknowledge that the possibility exists that the virus was synthesized. Speaking before the UN in New York on Wednesday, Lentzos presented the work of the Independent Task Force on Research with Pandemic Risks, which calls on scientists the world over to follow stricter regulations lest another worldwide breakout occur, the Telegraph reported. “We have to acknowledge the fact that the pandemic could have started from some research-related incident,” Lentzos said. Advertisement “Are we going to find that out? In my view, I think it’s very unlikely that we will. We need to do better in the future,” she added. “We are going to see more ambiguous events.” https://nypost.com/2024/02/29/world-news/scientists-may-have-started-the-covid-pandemic-article/ https://telegra.ph/Scientist-claims-smoking-gun-evidence-COVID-19-intentionally-created-by-researchers-in-Chinese-lab-03-11

BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome 2nd Smartest Guy in the World This important article further establishes that the Modified mRNA “vaccines” integrate into the cells. While these contaminated cells do not express the entire spike protein, but, rather, only part of it, the net effect is that the DNA of the “vaccinated” is irrevocably altered. Any type of integration into the genome, especially when being assaulted by millions of different random sequences from the “vaccine,” will inevitably cause mutations and other damage to the genome, irrespective if the entire spike protein is expressed, or not. This DNA contamination ultimately results in the plethora of slow kill bioweapon adverse events that we are now seeing in surging amounts, not limited to prion diseases, turbo cancers, SADS, and so on and so forth. The below is translated from Japanese, and it is a rather technical read, but well worth your time. by Mao Arakawa (Okudo Hirokushi) The essence of the corona vaccine contaminated DNA problem is the possibility of altering the human genome. To validate this possibility, Dr. Ulrike Kaemmerer conducted an experiment to administer the corona vaccine to MCF7 and OVCAR-3 cancer cell lines. Dr. McKernan, consulted by Dr. Kaemmerer, conducted an experiment to detect contaminated DNA from these cell lines. He reports on his blog the first case of contaminated DNA integration into the cancer cell line genome. (2SG: yesterdays article entitled, UPDATE: Doctors Warn mRNA "Vaccines" Could Spur Epidemic of Prion Brain Diseases addresses this.) I was interested, so I attempted to recreate the DNA recombinant event that Dr. McKernan identified. In this article, I will show the results of my analysis. Nepetalactone Newsletter Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2 Ulrike Kaemmerer has treated MCF7 and OvCar3 cancer cell lines with various vaccines. Once transfected they performed cell passaging on these transfected cell lines to dilute out the residual vaccine and identify cells which were transfected. They performed Immunohistochemistry (IHC) on these cells and documented spike expression levels… Read more 14 days ago · 109 likes · 22 comments · Anandamide image Figure 1 Dr. Kaemmerer administered the corona vaccine from Pfizer and AstraZeneca to the ovarian tumor cell line OVCAR-3 and, after subculture, confirmed the expression of the spikutanpak by immunohistochemical staining. Deep Sequencing comes at a high cost; therefore, preliminary experiments are required in advance to perform DNA detection experiments. Dr. McKernan first screened post-vaccination cells with qPCR and targeted qPCR-positive cells for deep sequencing. Contaminated DNA that is not integrated into the genome is diluted with subculture. In fact, the Ct value of the vector was Ct 30.28 in the first generation, but it was 34.72 in the second generation. The difference in 4Ct is 16 times the difference, and that is the lower concentration in the second passage. Dr. McKernan extracted DNA from two cells subcultured and performed deep sequencing. Sequence data detected SV40, replication origin and spiked DNA. Spike DNA was detected in the full genomic shotgun library of vaccine-treated samples with 3000x coverage. (Coverage means the percentage of the total base pair or locus of the genome covered by sequencing.) Since the coverage in the human genome was 30 times, we can see that the DNA with a large number of copies of the genome was invading the cell. As a result, strangely, SNP (monobasic polymorphism) was detected in deep sequencing at the origin of the vaccine plasmid replication (F1 and SV40). This SNP does not exist in the vaccine. In other words, it seems that plasmids are mutating in cells. Also, the coverage of deep sequencing in the replication origin area is higher than average, and the number of copies observed is relatively high, which means that the DNA embedded in the cell may be duplicated and mutated. I mean. Originally, plasmids and SV40 DNA replication require specific enzymes not owned by human cells. Experiments such as the introduction of large amounts of microDNA fragments containing replication points into cells are not usually performed in molecular genetics. It is possible that unexpected DNA replication is occurring within the cell. A total of two genomic integrations were observed in the vaccinated cell line from the analysis of Deep Sequencing by Dr. McKernan. Individual arrays of deep sequencing are called 「 leads 」. It was very interesting data, so I tried to re-parse the lead myself. image Figure 2 Figure 2 is a lead showing genomic integration in Dr. McKernan's Deep Sequencing Analysis. The subject of the analysis is Genome Integration Leads 1 and 2. You can also read a lot of information from short array data. This time in comparison with the human genomeblat searchTo find homologyblast searchI used it. Now, after that, it will be my own re-parse. image Figure 3 The top of the array in Figure 3 is the lead. As you can tell by aligning this lead with the 12th chromosome (black) and the spike gene (red) of the Pfizer Corona vaccine, the 12th chromosome (black) is on the way to the spike gene (red). I am switching. And there is a short identical array (here GAGAG) in the place of switching. You can see that the end-recombination (MMEJ, Microhomology-mediated end joining) mediated by microhomology (microhomology) recombinates the contaminated DNA and human genome. Since MMEJ involves multiple intracellular DNA repair enzymes, this recombination is an artifact (mistake product) in the test tube. Instead, gene recombination may have occurred in cells. Genome integration occurs on the long arm of chromosome 12, and the FAIM2 gene is present at this locus. FAIM2 is a gene that has been suggested to be associated with cancer malignancy. Recombinations occur on introns (arrays that do not encode proteins), but I do not know how such mutations also affect gene expression. image Figure 4 Another example of genomic integration is Figure 4. If you align this lead with chromosome 9 (black) and spike gene (red), you can see that in the lead, chromosome 9 (black) is switching to the spike gene (red) on the way. There is a short identical array (here TCTGCCCT) in the place where this example also switches. After all, it is believed that the contaminated DNA and the human genome were recombined using microhomology. Since there are multiple pathways for DNA repair, which repair pathway is used when foreign DNA is taken into the genome is case-by-case. Part of the lead had an Illumina adapter array left. Adapter arrays are arrays granted to PCR amplify and sequence DNA for deep sequencing. Originally, the adapter array is removed during parsing, but often the removal is inadequate and remains in the lead. Integration of contaminated DNA into the genome is occurring near Centromea. Let's talk a little about Centromea. Two chromosomes with the same genetic information that can be done after DNA replication are chromatids (sister chromatids). The chromatids are connected until the chromosomes are distributed during cell division, but the region on the connected DNA is Centromea. As such, Centromea is an important area for chromosome separation and distribution. image Figure 5 Figure 5 is about the DNA fragments of the spike gene integrated into the genome. On the Pfizer Corona vaccine spike gene, the sequence found in the genome integrated lead was written in red. Due to lead length limitations, the actual integrated array will be even larger. The integrated sequence is part of the spike gene, and it is not possible to make a full-length spike sequence. However, it is unpredictable how contaminated DNA will be inserted into any area of the genome and have any effect. image Figure 6 Nucleotype (cario type) means the size, shape, and number of chromosomes. Human chromosomes consist of a total of 46 22 pairs of autosomal and one pair of sex chromosomes. The autosomal is assigned the number 1 chromosome, number 2 chromosome,, number 22 chromosome and number in order of size. The integrated site of contaminated DNA is the FAIM2 locus on the long arm of chromosome 9 and near Centromea on chromosome 12. The genomic integration observed this time is the first two cases in cultured cell experiments, but the specific identification of recombinant sequences with the human genome of contaminated DNA is a major advance. Further verification experiments will be advanced in the future. Genome integration, as in Figure 6, does not know which locus actually occurs on the genome. This is exactly the 「 shotgun attack on the genome 」. What happens in cultured cells can also occur in normal cells, with a wide variety of alterations depending on the site of genomic integration. The first predicted catabolism is cancer induction and malignancy. And then, the ones that manifest themselves over time are various genetic diseases. What is known as a factor that causes genomic damage is, for example, radiation exposure, but genomic modification by contaminated DNA is different in that it is due to fragments of artificially created genes, and random mutations which are akin to radiation. But it is fundamentally different in nature. This experiment in cultured cells epitomizes genomic integration of contaminated DNA. This is a real problem that a large number of humans around the world, under the name of vaccination, are now experiencing a「 transfection human body experiment 」of contaminated DNA. The genomic modification of humanity is a direct consequence of the largest experiment in history of mRNA drug substance harm, and in the future it may be etched in history as the「 original sin 」of humanity. Original Social Engineering Sin Original Social Engineering Sin “...the socio-psychological foundations of socialism is identical to that of the foundations of a state, if there were no institution enforcing socialistic ideas of property, there would be no room for a state, as a state is nothing else than an institution built on taxation and unsolicited, noncontractual interference with the use that private people c… Read full story They want you dead. Do NOT comply. Upgrade to paid Shop 2SG merch Use code 2SGPET for 10% off PetMectin Use code 2SGPET for 10% off PetDazole Use code 2SGPET for 10% off FishCycline BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome 🧬 https://www.2ndsmartestguyintheworld.com/p/breaking-integration-of-corona-vaccine https://telegra.ph/BREAKING-Integration-of-corona-vaccine-contaminated-DNA-into-the-human-cell-line-genome-03-11

ASDI Project ▶ The mined tokens can be transferred to the metamask. ▶ It is a token that is likely to be listed by ASDI Group, and please preempt it. ▶ Click every hour (it's a good idea to set an alarm)  ※ Subscription link  Android : https://play.google.com/store/apps/details?id=com.asdi.nft IOS : https://apps.apple.com/kr/app/asdi/id6471332498 Invitation code: 0xccd36c074ab864bd8946ecae223c06d69b60c970 ▶ Mining Method 1.Click on the top of the first screen (guest). Link your account to your MetaMask BNB chain address. Click "AGREE AND SIGN" to switch to the ASDI screen. Click "Signature" in Metamask, switch to ASDI screen. Click "Menu" on the bottom right of the first screen, and check your reference. (The BNB wallet address is your invitation code.) Invitation code: 0xccd36c074ab864bd8946ecae223c06d69b60c970 Enter the invitation code in My inviter and click Done. After clicking Confirm, (Go to the first screen after checking the recommendation) Press and hold the mark between Overall and Daily mission to start mining. Enjoy your preoccupation.

The Rothschild Deep State Cabal Is Imploding Jonas E. Alexis, Senior EditorFebruary 23, 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. Whenever any form of government becomes destructive of these ends [life, liberty and the pursuit of happiness], it is the right of the people to alter or abolish it, and to institute new government, laying its foundation on such principles, and organizing its powers in such form, as to them shall seem most likely to effect their Safety and Happiness. Thomas Jefferson, Declaration of Independence, 1776 That same momentous year that kicked off the American Revolution, 1776 was also the year that ex-Jesuit Adam Weishaupt in Bavaria founded his Illuminati Order, sponsored by Mayer Amschel Rothschild as House of Rothschild patriarch in nearby Frankfurt, Germany. And it was America’s third US President Thomas Jefferson, who refused renewal of the Rothschild controlled First Bank of America’s charter in 1811. The American Revolution may have been fought for independence from King George’s British monarchy, but not independence from the Rothschild central banking cartel, whose controlling 70% foreign interests in First Bank of America indebted America’s earliest citizens. At the end of George Washington’s eight years as first US president, in 1791 the federalist Rothschild agent Alexander Hamilton installed for the Rothschilds their First Bank of America. Not renewing its charter, Jefferson kicked the Rothschild owned bank out of the US, which became the basis for America’s first war as a sovereign independent country, once again facing the same British enemy in the War of 1812. This war fought over financial independence from Britain’s City of London, only caused young America to drown further in war debt, as Nathan Rothschild backing both sides to every conflict he creates was determined to bankrupt the US to force it into recolonization. Despite the hard-fought American military victory, by 1815 with the US war debt nearly tripled at $119.2 million in the red, America financially was already a major debtor nation owing the infamous bloodline banking dynasty. That same year, making a colossal fortune over the Battle of Waterloo outcome by pre-rigging his investment, the gloating crook Nathan Rothschild proclaimed: I care not what puppet is placed upon the throne of England to rule the Empire on which the sun never sets. The man who controls Britain’s money supply controls the British Empire, and I control the British money supply. Sadly, America’s War of 1812 struggle for financial independence from the Rothschild controllers was lost. A brief excerpt from my Pedophilia & Empire series, Book 3, chapter one on the Rothschild family: In 1816 with yet a Second Bank of the United States foisted on American citizens for the next 20 years, in effect, Rothschild was simply seizing his predatory ownership of the United States. And once again, private control over the US money supply tacking on parasitic interest went into the coffers of as many as 1000 foreign investors, with [Nathan’s younger brother] Baron James de Rothschild in Paris holding the controlling shares. When the Second Bank of America’s charter was up for renewal 20 years later in 1836, that year Nathan Rothschild died. But France’s James de Rothschild assuming control over both the London and Paris banking branches, battled playing dirty as usual for charter renewal. He met his match as the resolute, feisty President Andrew Jackson was up for the challenge, declaring war on the House of Rothschild: You are a den of vipers. I intend to rout you out and by eternal God, I will rout you out. President Jackson’s turn to oppose the centralized moneychangers ultimately proved successful, kicking the Rothschilds out of America yet again, and the second British dynasty US takeover was again foiled, at least temporarily. However, the year prior in 1835, amidst the battle over the US private central bank, Jackson barely dodged a bullet to literally escape an assassination attempt attributed to Rothschild wrath. From 1836 to 1913, the US was largely free of the treacherous Rothschild leeches from Europe, signifying America’s longest period of foremost economic growth and prosperity in its entire history. Having acquired central banking control over Europe and through Nathan Rothschild’s ownership of the Bank of England by early 19th century, the British East India Company monopoly over international trade, including both the drug and slave trade, spanned the globe from Africa, the Indian and Pacific Oceans to North America and Europe, the flourishing international banking cartel consolidated its growing global money lending power over every commercial trade on every continent. But one vast sprawling nation covering two continents over the centuries resisted and eluded the Rothschild clutches. As a result, Russia was repeatedly targeted, as its ruling Romanov monarchy managed to successfully evade the Rothschild predatory conquest, but not without murderous retribution. From author Eustice Mullens’ New World Order: After the fall of Napoleon, the Rothschilds turned all their hatred against the Romanovs. In 1825, they poisoned Alexander I; in 1855, they poisoned Nicholas I. Other assassinations followed, culminating on the night of November 6, 1917, when a dozen Red Guards drove a truck up to the Imperial Bank Building in Moscow. They loaded the Imperial jewel collection and $700 million gold, loot totaling more than a billion dollars. The new regime also confiscated the 150 million acres in Russia personally owned by the Czar. In addition to a century of assassinating Romanov czars by poison, when Czar Alexander II came to the aid of Abraham Lincoln during the Civil War, which by many accounts attribute Russian support to preserving the Union, the vindictive Rothschild cartel as primary backer of the Confederacy, vowed eternal revenge against the Russia and its royal family. The Rothschilds et al’s war at all cost against Russia today in Ukraine is merely this same long legacy’s outcome. Just prior to the Rothschilds’ planned First World War in 1914, a few months earlier in late 1913, they deceptively snuck through Congress their Federal Reserve Act on December 23rd, after most members had already left on Christmas break. The Jekyll Island rendezvous of the Fed Reserve architects included Paul Warburg, the German born chief central banking Rothschild agent moved to the US, ending up the second Vice Fed chairman. Continuity of one thought mind pervades the Warburg clan as Paul’s son James Paul Warburg before the Senate Foreign Relations Committee in 1950 emphatically declared: We shall have world government, whether or not we like it. The question is only whether world government will be achieved by consent or by conquest. Thus, the third Rothschild central private bank in America was established to take permanent full usury-debtor system control over the US money supply, through bribery of Washington’s political puppet class, and the American people through their engineered debtor system. 1913 also saw the passage of the Federal Income Tax Act, illegally squeezing tax dollars to rip off hardworking US citizens just to pay off debt interests from all the bankers’ war loans. This vicious control cycle is how Khazarian mafia swindlers have cunningly operated since their identity snatching days of their ancient Khazar kingdom over a millennium ago. The Rothschild central banking controllers hired one of their own, distant cousin Karl Marx to write his Marxist Communist Manifesto in 1848. And it was the Rothschild cartel money along with Rothschild agent Jacob Schiff in America that financed his fellow Jews’ Bolshevik Revolution and their plotted murder and theft of Russian Czar Nicholas II’s family in 1917. And that billion plus of stolen Russian gold is said to have wound up stored in Rothschild’s underground chambers at City of London’s Bank of England. A centuries long pattern of covert deception, murder, war, corruption and insatiable appetite for greed and increasing power characterize all that is behind today’s still operating Khazarian mafia bankster dynasty rooted in ancient Khazar more than a millennium ago. Closer to this century historically, one world government tyranny and depopulation eugenics have both reflected the elites’ obsession. Rothschild crimes funded all three of the most bloodthirsty dictators in all of human history. The 1917 Russian Revolution spawned the rise of the Lenin-Stalin Communist Soviet Union democide, killing 66 million mostly Christian Russians. Then, since the early 1930s, in addition to Bush, Rothschild and Rockefeller bloodlines also funded the rise of Adolph Hitler. His alleged sacrifice of 6 million Jews in WWII was used coldheartedly as Zionist bargaining chips for the non-Hebrew Ashkenazim false claim of “Israelite birthright” to a homeland in Palestine, promised to Lord Lionel Rothschild in the 1917 Balfour Declaration. Three decades later, the pledge was fulfilled with the establishment of the Jewish State. Despite a non-Hebrew heritage, Ashkenazi [non]Jews that trace back originally to nomadic Turkic tribes, comprise 90% of today’s Israeli population. The Balfour Declaration also made another pledge: …Nothing shall be done which may prejudice the civil and religious rights of existing non-Jewish communities in Palestine. The Jewish State since its 1948 inception, that’s the last three quarters of a century now, has brutally pushed out the true Semite Arabs living in Palestine, their rightful ancient homeland, yet they’ve been systematically destroyed by Israel’s official genocidal apartheid policy. This fact is neither anti-Semitic nor what should be allowed or tolerated by rest of the world, yet with impunity, it has for far too long. This shameful reality is largely due to the Zionist House of Rothschild’s influence and control over Israel. Also in the 1930s, the Rothschilds groomed and backed yet another notorious Yale educated dictator Mao Zedong, also covertly supporting his democide against 65 million of his own sacrificed fellow Chinese. Over the centuries, you can recognize a pattern, that these Luciferian bloodline controllers led by the likes of the Rothschild and Rockefeller dynasties, have had ample practice committing genocides, financing the rise to power of all three dictators responsible for the deadliest genocides in all of history on this planet… that is, until the current unprecedented genocide against today’s human race. In 1933 the globalists of the day attempted the first major coup against the United States government in a failed attempt to overthrew the Franklin Delano Roosevelt, singlehandedly prevented by the Medal of Honor and most decorated war hero US Marine Corps Major General Smedley Butler. His intervention stopped the plotted criminal takeover, exposing it publicly in the press in 1934 as well as in his book. And though his courageous actions successfully averted the treasonous subversion committed by some of America’s wealthiest, most powerful conspiratorial traitors as captains of industry, bankers and politicians, among them heir to the Singer Sewing fortune Robert Sterling Clark and George HW Bush’s father, Prescott Bush, during WWII as a Union Banking Corp. director, Bush’s company was linked to financing, aiding and abetting the US Nazi enemy Adolph Hitler, yet his shockingly treasonous past was covered up and he was sent to the US Senate from Connecticut. Of course, the Bush-Clinton crime families are notorious for getting away with multiple felonies of high treason. Pedophile George Bush senior was implicated in America’s largest publicly exposed child sex trafficking network, tagged the “Franklin scandal” involving Nebraska children some from Catholic Boys Town directly trafficked to the White House during the Reagan-Bush administrations. While the Bush crime family are Satanists, their fellow Satanist arrested in this scandal coverup was fall guy Lawrence E. King, though the entire operation was quickly swept under the carpet as ringleader King aided by the likes of Satanist Lt. Col. Michael Aquino hotel drop-off of a cash filled suitcase to King. Like Epstein, Lawrence King was also handed a sweetheart deal with next to no jailtime considering his ungodly crimes. Of course, Aquino always walked free despite being linked to multiple pedo-scandals, protected by his military status high up in America’s MK mind control operation, identified by a number of child victims at the Presidio daycare scandal as well as implicated by Cathy O’Brien as a MK-ultra top programmer. America’s highest-profile pedophile-child sex trafficker is supposedly deceased, Jeffrey Epstein, while his gal pal partner-in-crime Guislaine Maxwell serves her 20-year sentence in a Florida federal penitentiary. Whereas the Franklin scandal incriminates the Bush crime family, both the Epstein-Maxwell operation and Pizzagate scandal expose the Rothschild, Clinton, Podesta, Obama, Biden crime families, including Donald Trump touting what “a terrific guy” Epstein was to 2004 New York Magazine, adding how he loves “the young ones,” wink, wink. The fact is, America’s uniparty is infested with hundreds of compromised famous pedophiles and gatekeeping enablers still walking free, despite the tons of cameras capturing the crimes as evidence. Outside of King, Epstein and Maxwell, zero arrests and prosecutions of any prominent guilty pedo-criminals including British, Belgian, and Dutch royalty, prime ministers and presidents, as well as billionaire criminals like Bill Gates, hundreds, perhaps thousands of these blackmailed VIP politicians, judges, police chiefs, generals, CEOs, bankers and entertainers, all guilty of horrific child sex abuse crimes have yet to face their unholiest of unholy karma. Multiple chapters in Pedophilia & Empire Book 4 unravel the US pedo-scourge and other scandals throughout the world in the other books. The New World Order, secret societies and the global pedophilia network generating enormous black ops revenue involving colossal amounts of money laundering by all Rothschild private central banks, are explicitly intertwined and fully documented in the five volume series with access to all 50 plus chapters here. Because so much accelerated shocking truth is coming out weekly, with a one in 6 billion chance of so many disastrous chemical spill derailments all at once, manmade earthquakes punishing nations aligned with Russia, all are only further incriminating the bloodline controllers and their puppet minions at the highest echelons of Western power. The reason why the Ukraine war is so huge right now, carrying so much at stake, is because the entire New World Order’s one world government scheme is riding on the bloodline controllers’ defeat by Russia in Ukraine as their longtime “devil’s playground” hub gets further exposed to the global public. With all these bloodline criminals vis-à-vis the Rothschild dynasty atop this predatory food chain, busily bribing, blackmailing, and silencing facts and truthtellers through any and all means necessary, it’s to ensure that their psychopathic club of elites remains unreachable and immune from all prosecution and long overdue justice. They know more than enough criminal evidence is out there in the public domain to convict these genocidal killers for their unending crimes and they know that We the People are closing in on them. And because of this, the monstrous beasts are willing to unleash nuclear Armageddon. We are living through epic times, and though millions have already perished and perhaps billions more will follow, in this war between good and evil, we have them on the run, rushing like cockroaches for the cover of darkness. But armed and united by the truth, justice will be done. As a consequence of the covert subversive overthrow of the United States government taking place in recent years, both the complete absence of rule of law and rampant treasonous failure to uphold the US Constitution, currently has Americans and people around the world waking up in righteous anger by the thousands every single day. Our founding fathers like Thomas Jefferson bestowed fundamental rights of liberty and freedom to every citizen, granting us clear-cut legal justification and guidelines to, in his words, “abolish” the illegitimate treasonous regime occupying Washington today. Taking into account the US government’s repeated terrorist acts constituting democide against its own American citizenry as well as having committed acts of war against US closest allies like Germany via the Nord Stream sabotage, the Biden regime’s intent to destroy both America and West must be opposed immediately. A growing majority of Americans disapprove of Biden’s job performance as imposter president, more so than any previous president in US modern history during the entire 78 years of presidential poll ratings. After the US Supreme Court declined the Brunson case out of Utah last month for a second time this year, the longshot effort to hold the vast majority of Congress accountable for illegally ratifying a fraudulent, rigged 2020 election has been thwarted. All three branches of government – the executive, legislative and judiciary, have systemically failed Americans by repeatedly violating the US Constitution in clear breech of their sworn oaths to uphold and defend. All three branches have committed treason for destroying our nation through reckless, willful crimes endangering both the American as well as global population, targeted for extermination by the elites. Nuremberg 2.0 needs to immediately be invoked for mass tribunal trials of multitudes of genocidal traitors determined to impose their diabolical, exposed depopulation agenda on humanity. The assassination of John F. Kennedy, the president that vowed to “splinter the CIA into a thousand pieces,” reduce the power of the Federal Reserve and avert a decade long costly war in Vietnam, set the stage for the Deep State to fester and thrive ever since November 22, 1963. Every US president ever since has been a mere puppet for bloodline controllers to rape the earth and humanity in the name of the military industrial security Big Pharma complex. In this century the Khazarian mafia infested and controlled international criminal cabal manufactured their “new Pearl Harbor” 9/11, an Israeli-neocon grand Satanic blood sacrifice after the prewritten Patriot Act straight out of the dialectical “problem, reaction, solution” con-game playbook intended to strip away all Americans’ constitutional rights, a lose-lose our less freedom for less security and win-win for the Satanists, thinly disguised as collateral damage behind their fabricated war on terror against Muslim terrorists they create, train and finance as fake proxy war US enemies, supplementing their ongoing “war on drugs” to destroy African American families for the prison security complex, then when convenient again switch the revolving “enemy” back to the Russians and Chinese in Cold War #2 to drive humanity off the Armageddon cliff with today’s nuclear World War III countdown. And now along with the threat of a mushroom cloud, their enemy target today expands to a genocidal war against the entire human species with their fake pandemic/killer jab’s malevolent agenda to destroy national sovereignty via the United Nations’ World Health Organization, subversively imposing more fake or deadly health emergencies possessing an unlimited bioweapon arsenal bringing more draconian lockdowns, more killer mandates, along with their 15-minute smart cities control grid prison enslavement, planetwide mass surveillance, Chinese modeled social credit scores freezing dissidents’ bank accounts requiring digital ID approval and cashless World Bank Digital Currency, all part of their “Great Reset.” The globalists’ wet dream is our never-ending nightmare of absolute myopic control over the culled down, beaten down, traumatized, lobotomized population of jabbed, DNA altered, group hived, AI mind-controlled cyborg survivors. This is our bleak Lucifer controlled future if we remain weak, passive, defeated and ignorant. Activism is growing in a planetwide movement protesting against the Ukraine debacle along with the price inflation, smart cities and World Economic Forum’s enslavement. Legal challenges against the technocratic tyranny, the genocide, the wokist insanity. Our enemy is on notice and no doubt will be unleashing more false flags and WMDs at us, but the momentum of growing resistance and opposition is mobilizing for the long war. Joachim Hagopian is a West Point graduate, former Army officer and author of “Don’t Let the Bastards Getcha Down,” exposing a faulty US military leadership system based on ticket punching up the seniority ladder, invariably weeding out the best and brightest, leaving mediocrity and order followers rising to the top as politician-bureaucrat generals designated to lose every modern US war by elite design. After the military, Joachim earned a master’s degree in Clinical Psychology and worked as a licensed therapist in the mental health field with abused youth and adolescents for more than a quarter century. In Los Angeles he found himself battling the largest county child protective services in the nation within America’s thoroughly broken and corrupt child welfare system. The experience in both the military and child welfare system prepared him well as a researcher and independent journalist, exposing the evils of Big Pharma and how the Rockefeller controlled medical and psychiatric system inflict more harm than good, case in point the current diabolical pandemic hoax and genocide. As an independent journalist for the last decade, Joachim has written hundreds of articles for many news sites, like Global Research, lewrockwell.com and currently https://jameshfetzer.org. As a published bestselling author on Amazon of a 5-book volume series entitled Pedophilia & Empire: Satan, Sodomy & the Deep State, his A-Z sourcebook series exposes the global pedophilia scourge is available free at https://pedoempire.org/contents/. Joachim also hosts the Revolution Radio weekly broadcast “Cabal Empire Exposed,” every Friday morning at 6AM EST (ID: revradio, password: rocks!). 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/2024/02/the-rothschild-deep-state-cabal-is-imploding/

What If Everything They’ve Been Telling You About Food Is… WRONG? Vigilant NewsFebruary 2, 2024 By Brian Cates The last 9 months have been an exceedingly strange journey for me. While I had already figured out the FDA food pyramid was garbage and had watched in real-time as all the federal “medical” “health” “science” agencies played a direct role in suppressing accurate information on COVID-19 and C-19 origins, treatments, vaccines, etc., it took me the better of part of 3 years to begin critically and logically examining what these self-same propagandists disguised as ‘experts’ have been telling all of us about food and what supposedly comprises a healthy diet. I’d struggled with my weight since I was a young man of 24. I am soon turning 60. I’d spent the past few years talking about losing weight and the all the issues I was dealing with from lugging around over 100+ pounds of useless bodyfat. But I was still eating 4-5 times a day, at least two of those meals being sizable. And though I cut down on the sweets and was eating what I was told were ‘healthy whole grains’, the weight not only refused to go down, it kept going up. I would go through the same cycle several times from when I was around 26 to last year: Start working out religiously, while eating what I was told was mostly ‘healthy’ food. I’d add some muscle, my weight would drop maybe 20 pounds or so…and then after 3-4 months, hit the wall. No changes, and despite working out, the weight crept back up. Quit working out, gain all the weight back, a year goes by…then start the cycle again. 34 years or so I ran on this hamster wheel. When this picture was taken, I’d just started writing for The Epoch Times in mid-2018. I was 350 pounds or so. Hadn’t weighed myself in a while. I was too scared to look anyway. Image I had just gone through the cycle again early last year. Working out, eating the “healthy food” chock full of carbs, various forms of sugars and toxic seed oils & chemicals, etc., etc. Then in May, I quit again. In late June, my stepmom visited me in my new house in Florida while I was on an RV tour around the US, and when she saw how I was living and eating, she read me the riot act. She kicked me in the ass and got me not only moving again, but that visit was also the catalyst I needed to go back and re-examine 35+ years of failure and why trying the same thing over and over again wasn’t working. For years, people like me were told this was a willpower/laziness thing. You’re fat and you can’t lose the weight because you don’t eat right/work out hard enough or long enough, etc. So I was mentally beaten down after exhausting myself on this hamster’s wheel as I was headed into decade #4 with the wrong programming in my head. Overweight Man Tired after Training, with Hand on Forehead Against ... But here’s the thing. As a journalist, I’d just spent the last 3 1/2 years extensively and exhaustively covering how federal and state and county ‘health’ ‘medical’ and ‘science’ ‘experts’ had just engaged in a deliberate conspiracy to hide and censor true and accurate information from the American public. Not to mention also covering the amount of gaslighting we were all being hit with following the blatant theft of the 2020 election from Donald Trump. So at this time, in late June/early July of last year, I started my re-examination of around 35 years of failure with an intriguing thought: **COULD IT BE** that the very same ‘health’ ‘medical’ & ‘science’ experts who’d just exposed and outed themselves as Big Pharma propagandists and business partners lying to us about COVID & many of the drugs involved in the treatment/prevention of infection…were also wrong or deliberately misleading us about….food? Image Could it possibly be…. One of the first things I realized, when I began examining what the federal ‘health’ ‘medical’ ‘science’ agencies tout as a ‘healthy’ diet, is that when they last changed the food pyramid in the early 1990’s, the rates of both obesity and diabetes exploded in this country as people began following this ‘expert’ advice. As you can see from the graphs below, an already alarming rising trend suddenly shot dramatically upward in the early 1990s. Image Image How bad has the obesity/diabetes/insulin resistance crisis gotten in the US? It is now so bad they’ve coined a bullshit term – ‘prediabetes’ – to try to mask the deadly seriousness of the crisis. If you are diagnosed as ‘prediabetic,’ you ARE diabetic; it’s just that your insulin resistance hasn’t progressed to such an extent that they’ll officially call it ‘diabetes.’ Image Or as actor Wilford Brimley would say: Wilford Brimley Has Diabeetus - Misc - quickmeme Insulin resistance leads directly to a massive amount of chronic health issues of which diabetes is only one. By giving Americans the ‘expert’ advice that they needed to start chugging down ‘6-11 servings’ every day of ‘healthy whole grains’ and cook their food with seed oils while counseling them to also **reduce** the amount of meat and animal fats they were eating, Americans began ingesting way more carbohydrates and PUFA’s [that’s ‘polyunsaturated fatty acids, for those of you in Rio Linda…] every day than they’d been eating before. And yet I recall for the past 30 years or so watching the popular culture health reporters scratch their heads and wondering what could possibly be causing the massive explosion of obesity and chronic illnesses, as well as the dropping testosterone and estrogen levels they were observing. So the fact that the federal ‘health’ agencies caused much of the country to make a dramatic wrong turn that exacerbated the rising trends of obesity and chronic illness with their drastically wrong official ‘food pyramid’ in the early 1990s, caused me to wonder: If they were giving the American public such rotten, terrible, horrible, no-good ‘expert’ instructions on what they should be eating every day, **what else** have they been telling us that is utter bullshit? And the very first thing I stumbled over in this regard was the history of SEED OILS and how medical scientists doing animal experiments back in the 1890s/early 1900s quickly established that seed oils were toxic and harmful to growing and developing animals. By the end of July last year, I was sharing the alarming stuff I was finding in my research with my readers on my Substack: Image You have to fully grasp this. They **knew** from animal experiments on rats and cows and horses and birds **exactly** what SEED OILS did to growing and developing animals. Many of these experiments were carried out from the late 1880s through the 1910s. Experiment results were published in books, such as this one from scientist E.V. McCollum in 1918. There was no mystery here. The results were established and easily observable. And yet…what ended up happening over the next 100 years? Government ‘health’ experts working hand-in-glove with Big Food corporations convinced most Americans to stop cooking their food with butter, lard, and tallow, and instead use the new ‘Crisco’ and other highly processed seed oils and margarine. Because they claimed these new processed products were ‘healthier’. And because Americans back then were very trusting people who didn’t know their government was controlled by hidden corporations and interests out to make massive profits while not caring about their health, they followed this ‘expert’ advice from authority figures they were taught to trust. From the 1920s through today, Big Food, working in conjunction with Big Government, began creating many new highly processed foods that contained large amounts of these seed oils and myriad toxic chemicals and food additives. Our American culture is now flooded with highly processed fake ‘food’ that didn’t exist even 100 years ago. And they are inventing new kinds of fake food every year. Image If they knew what seed oils would do to human beings who began eating them early in life, and ate them throughout their physical development and into adulthood – and evidence seems to suggest they did – then the only possible reason for them to do that would be to arrest the development of children, cause chronic illnesses throughout life, and ensure a premature death. What I saw through my research was **deeply disturbing to me**. Image This can’t be just about profit motive, the fact they’d make a lot of MONEY creating new addictive processed sugar-and-carb-and-seed oil-filled foods. They had to also have seen the very real and OBVIOUS HARM they would be doing to their fellow citizens by introducing these heavily toxic and health-destroy products into the American food supply. Not when you realize the wealthy elite who run everything in this fallen world behind the scenes are constantly wringing their hands and brainstorming about how to ‘fix’ the world’s overpopulation problem, think even the concept of human rights is a big funny hilarious joke, and that human rights don’t exist, just like God doesn’t exist. They’ve always sat around at their big, important conferences in places like Davos and talked about culling the human herd like they’re ranchers planning for the next cattle drive. It’s just that they’re starting to get embarrassed that the cows are now spying on them in the barn and figuring out what they’re talking about, their plans for the rest of us. What more clever way could be devised than convincing people to simply EAT themselves into chronic illnesses that will guide them expeditiously into an early grave? The rise in life expectancy rates over the past 100 years is not because people are HEALTHIER overall. Image Far from it. The rates rose because of medical advancements in keeping chronically ill people alive longer. Were people not being tricked and misled into fattening themselves with constant insulin resistance and filling their bodies with toxins, most people would very likely be living into their upper 90s by now. Instead, life expectancy is dropping because the amount of toxic and unhealthy food Americans are eating is going up. This cannot be overstated. With the medical/health/scientific advancements in knowledge and technology over the past 120 years, the only way this was allowed to happen and to become so widespread at this point millions of people are dying from easily preventable chronic illnesses is that… …and I know some of you will struggle to accept this…. …the real owners of the world out there **wanted** this to happen. They demanded it. There’s no way they don’t know. So if they know…and nothing’s been done to stop it? It’s not just about money. There’s what looks like an exceedingly nefarious agenda at work here. Image Sometimes in my more paranoid moments, I wonder if…. Nah. Couldn’t be…. Could it? Image Tastes like chicken! https://www.youtube-nocookie.com/embed/W-JhfjGtlp8?rel=0&autoplay=0&showinfo=0&enablejsapi=0 So the first two things I discovered in my new research starting in the middle of last year: 1. The food pyramid was a massive ‘mistake’…or was it? 2. Seed Oils are toxic and harm human development and shorten the human lifespan Yet they were allowed to proliferate into the American food supply by accident…or was it really an ‘accident’? Next, I discovered that the conventional ‘expert’ findings about animal fat were wrong. For decades I’d been endlessly told and had read that too much dietary animal fat caused health/heart issues. Cut down dramatically on the red meat, the eggs, the butter, replace the fat with ‘healthy’ food… And yet what do you actually **FIND** when you examine the medical research? You find when people dramatically reduced their animal fat intake they still got FATTER and more CHRONICALLY ILL. After all, one of the biggest reasons for creating a ‘new and improved!’ food pyramid back in the early 1990s was to convince people to CUT the amount of meat and animal fat they were eating and replace them with ‘healthy’ carbs. For people who were supposedly becoming more ‘healthy’ by following the new food pyramid’s ‘expert’ advice, Americans seemed to be getting fatter, heavier, and more unhealthy. It’s been noticed for some time now that people in America in the 1940s and 1950s sure do look pretty darn healthy, even though we were constantly being told by our modern ‘health experts’ that those poor folks were eating WAY too much animal fats and red meat and eggs and [gasp!] butter. I mean…there’s just NO WAY that Americans back then eating all that bad stuff were healthier than US today, right? 🤔 Why, that very idea would be absurd! They didn’t know any better! They didn’t have our advantages! Image Image Image Hey…maybe it’s time for us to stop, go back and look, and rethink this all out again… Because SOMETHING clearly isn’t working. We’re **supposed to be** far healthier than those poor fools back in the 1940s and 1950s…but we’re NOT. Why is that? If you commit yourself to finding the truth and facing it unflinchingly, no matter where it leads…you can find it. The brutal truth is…people here in America have been misled. Just about EVERYTHING the ‘health’ and ‘diet’ ‘experts’ have been telling them all their lives is….SURPRISE!…wrong. It’s not your fault. It is THEIR fault. They either didn’t know what they were talking about when they were teaching you how to eat, or they had a hidden agenda. Either way…NOT YOUR FAULT. Image Image Image Its not that you lack willpower. Or that you’re lazy. Or that you don’t work out enough. Its that what the ‘experts’ taught you about how to eat a proper diet wasn’t true. You were not getting accurate information. You were steered towards unhealthy seed oil/sugar/carb-filled processed foods because authority figures you trusted gave you terrible advice. You were given bad information by government and medical authority figures on 7 dietary subjects: 1. Cholesterol levels 2. Salt/mineral levels 3. Protein levels 4. Animal Fats 5. Fiber 6. Seed oils 7. Meal frequency My research has led me to conclude that we need to go BACK to how our ancestors ate. A mostly meat diet where we do not eat large meals of highly processed fake foods several times a day with snacks in between. We’re not designed to put food into our stomachs 3-6 times a day, constantly spiking our insulin levels and hormonal system, developing lifelong insulin resistance and metabolic syndrome-related chronic illnesses and diseases. Especially not the kind of food we’re surrounded by in our popular culture, the highly over-processed stuff that didn’t exist 100 years ago that are now chock-full of toxic seed oils, sugars, and chemicals. Sure, people back in the 1940s and 1950s were eating 3 squares a day, but look at **what** they were eating compared to what we are surrounded by now. Until around 120 years ago, most people lived on farms, and even if they didn’t, most of the food they ate came almost directly from a farm. Have you heard stories about people who travel to Europe and visit places like France and Italy where they eat all the bread and pasta, drink all the wine they want, etc. and don’t get fat? Know why that is? Because it’s ILLEGAL over there in many European countries to add in the toxic chemical crap they put into US processed food on this side of the pond. Look at the following links for just a HINT of how bad this issue is. Why are European governments taking better care of their people’s health than our supposedly superior US government? https://www.cbsnews.com/news/us-food-additives-banned-europe-making-americans-sick-expert-says/ https://www.theguardian.com/us-news/2019/may/28/bread-additives-chemicals-us-toxic-america https://foodrevolution.org/blog/banned-ingredients-in-other-countries/ https://www.theguardian.com/environment/2022/jun/23/titanium-dioxide-banned-chemicals-carcinogen-eu-us Image So, when I began changing my diet again in 2023, I switched to a [O]ne [M]eal [A] [D]ay program [OMAD] where I ate only once time in every 24-hour period. I adopted a 4-hour ‘feeding window’ from 4 pm to 8 pm. I also cut out most of the processed foods I had been eating – including the Weight Watcher’s stuff. I increased the amount of meat I ate from around 1/3rd of my diet to 2/3rds. From late June through early September, I went from 345 pounds [my stepmom made me get on the scale with her watching. I expected to see around 320. Ulp!] down to 320. And then I got stuck. The weight stopped coming off and I fluctuated between 317 and 320 for around a month and a half. Then my ‘little sister from another Mister,’ investigative journalist and head editor of Uncover DC, Tracy Beanz, shared some pictures and testimony about her husband William, who had lost over 160 pounds on a Carnivore Diet in one year. He not only lost a massive amount of unhealthy body fat, but he also had several chronic health issues evaporate. Image Image So….in early November, I decided to cut out the bread and the potatoes and the ‘healthy’ cereal I was still eating and stay only with raw milk and unpasteurized cheese for my carbs, and the rest of my diet was Amish-farm raised beef, bison, chicken, turkey, and fish with large brown eggs. The weight started coming again…slowly. I went from 320 down to my current weight of 295. I’ve gone down to 293, but 295 is what I saw the last 2 times I weighed myself. So. I learned a lot in the last 8 months. I wanted to share some of what I learned in this thread. I am not telling or advising anyone to do what I’m doing. I’m providing information and asking for people to check this out for themselves and make up their own minds. A key part of The Great Awakening is, I am convinced, teaching people how to get healthy and stay that way. And if people have been getting wrong and perhaps even deliberate disinformation from ‘health experts,’ the more people realize that and start reassessing what they’ve been told over the past few decades? THAT’S A BEAUTIFUL THING. https://vigilantnews.com/post/what-if-everything-theyve-been-telling-you-about-food-is-wrong/ https://donshafi911.blogspot.com/2024/02/what-if-everything-theyve-been-telling.html

Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use. Brenda Baletti, Ph.D. global moratorium mrna covid vaccine feature Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science. Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review. The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule. After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail. Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs). Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials. They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.” They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters. “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote. Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies. It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender. “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added. According to McCollough, “mRNA should never have been authorized for human use.” Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.” Here are six takeaways from the review: 1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years. To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote. The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease. However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines. There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction. The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself. The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.” The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now 2. Steps were taken in trials to overestimate vaccine efficacy Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do. “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote. Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.” Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19. There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%. The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety. Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote. Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine. The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate. One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large. According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility. While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively. “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote. As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death. However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote. And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.” They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19. One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19. A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues. 3. The trials underestimated the adverse events, including death, despite evidence in the data. Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here. First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group. “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked. Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population. None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote. Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended. During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data. And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports. Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.” In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.” This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.” 4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary. Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population. The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants. Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.” After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke. And millions of AEs have been reported to those systems. Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system. In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems. The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious. In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal. “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.” 5. The failure to appropriately test for safety and toxicity poses serious problems. Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs. Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues. That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids. Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown. McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns. Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown. 6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness. The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines. “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection. They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself. They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants. https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/ https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html

Researchers urge governments to endorse a global moratorium on mRNA injections in a newly released science paper Rhoda WilsonJanuary 26, 2024 In a paper published on Wednesday, researchers re-analysed the Pfizer covid “vaccine” phase 3 trial data and found more serious adverse events among those in the vaccine group. This is not what published reports from Pfizer’s phase 3 trials said. “Many key trial findings were either misreported or omitted entirely from published reports,” the researchers said. Seven researchers – M. Nathaniel Mead, Stephanie Seneff, Russ Wolfinger, Jessica Rose, Kris Denhaerynck, Steve Kirsch and Peter A. McCullough – set out to re-analyse Pfizer’s trial data because: our understanding of covid vaccinations and their impact on health and mortality has evolved substantially since the first vaccine rollouts; and, problems with the methods, execution, and reporting of the pivotal phase 3 trials have emerged. On Wednesday, they published their findings in a peer-reviewed paper titled ‘Covid-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign’. The paper was published in Cureus, a journal of medical science. “Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group,” the researchers wrote. Adding, “Numerous SAEs were identified following the Emergency Use Authorisation (EUA), including death, cancer, cardiac events, and various autoimmune, haematological, reproductive, and neurological disorders.” The EUA the researchers are referring to is the authorisation granted to Pfizer by the US Food and Drugs Administration (“FDA”). As the paper noted, Pfizer’s covid “vaccines” never underwent adequate safety and toxicological testing according to previously established scientific standards. It goes on to detail the absolute risk reduction, the underreporting of harms during trials, the shifting narratives and illusions of protection, quality control and manufacturing process-related impurities, the biological mechanisms underlying adverse events (“AEs”) and why, based on how our immune systems work, the vaccine is ineffective. Concluding their comprehensive review, the researchers wrote: Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered. Mead M, Seneff S, Wolfinger R, et al. (January 24, 2024) COVID-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign. Cureus 16(1): e52876. doi:10.7759/cureus.52876none Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… The paper noted that the gene therapy products (“GTPs”) vaccine platform has been studied for over 30 years as an experimental cancer treatment, with the terms “gene therapy” and “mRNA vaccination” often used interchangeably. “Although we employ the terms ‘vaccine’ and ‘vaccination’ throughout this paper, the covid-19 mRNA products are also accurately termed gene therapy products (GTPs) because, in essence, this was a case of GTP technology being applied to vaccination,” they wrote. As such, throughout their analysis, the terms “vaccines” and “vaccinations” are used interchangeably with injections, inoculations, biologicals, or simply, products. The following are some excerpts from the paper. You can read the full paper HERE. Serious Harms Revealed after EUA was Granted In this narrative review, we revisit the registrational trials and review analyses of the AEs from these trials and other relevant studies. Most of the revelations have only recently come to light, due to the past few years of extensive censorship of healthcare professionals and research scientists who challenged the prevailing narrative set forth by the vaccine enterprise. Despite the rhetoric, no large randomised double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalisation or death. The study designs for the pivotal trials that led to the EUA were never intended to determine whether the mRNA inoculations could help prevent severe disease or premature death. It was only after the EUA that the serious biological consequences of rushing the trials became evident, with numerous cardiovascular, neurological, reproductive, haematological, malignant, and autoimmune SAEs identified and published in the peer-reviewed medical literature. Moreover, the covid mRNA vaccines produced via Process 1 and evaluated in the trials were not the same products eventually distributed worldwide; all of the covid-19 mRNA products released to the public were produced via Process 2 and have been shown to have varying degrees of DNA contamination. The process-related impurities were absent from the covid-19 mRNA products used in the registrational trials. Virtually all doses used in those trials originated from “clinical batches” produced using what is known as Process 1. As a post-authorisation emergency supply measure for global distribution, however, a method much more suitable for mass production known as Process 2 was devised utilising bacterial plasmid DNA. The failure of regulatory authorities to heretofore disclose process-related impurities (e.g., SV40) has further increased concerns regarding safety and quality control oversight of mRNA vaccine manufacturing processes. Incentives Played a Key Role in Undermining Scientific Evaluation Political and financial incentives may have played a key role in undermining the scientific evaluation process leading up to the EUA. Before the pandemic, the US National Institutes of Health invested $116 million (35%) in mRNA vaccine technology, the Biomedical Advanced Research and Development Authority (“BARDA”) had invested $148 million (44%), while the Department of Defence (“DOD”) contributed $72 million (21%) to mRNA vaccine development. BARDA and the DOD also collaborated closely in the co-development of Moderna’s mRNA vaccine, dedicating over $18 billion, which included guaranteed vaccine purchases. This entailed pre-purchasing hundreds of millions of mRNA vaccine doses, alongside direct financial support for the clinical trials and the expansion of Moderna’s manufacturing capabilities. Once the pandemic began, $29.2 billion – 92% of which came from US public funds – was dedicated to the purchase of covid-19 mRNA products; another $2.2 billion (7%) was channelled into supporting clinical trials, and $108 million (less than 1%) was allocated for manufacturing and basic research. Using US taxpayer money to purchase so many doses in advance would suggest that, before the EUA process, US federal agencies were strongly biased toward successful outcomes for the registrational trials. Established Vaccine Testing Period Abolished Before the rapid authorisation process, no vaccine had been permitted for market release without undergoing a testing period of at least four years. Previous timeframes for phase 3 trial testing averaged 10 years. Health departments have stated that 10-15 years is the normal timeframe for evaluating vaccine safety. The previously established 10-15-year timeframe for clinical evaluation of vaccines was deemed necessary to ensure adequate time for monitoring the development of AEs such as cancers and autoimmune disorders. Pfizer’s covid vaccine completed the process in seven months. Established Safety Standards Abolished With the covid vaccines, safety was never assessed in a manner commensurate with previously established scientific standards, as numerous safety testing and toxicology protocols typically followed by the FDA were sidestepped. Historical accounts bear witness to instances where vaccines were prematurely introduced to the market under immense pressure, only to reveal disabling or even fatal AEs later on. Examples include the 1955 contamination of polio vaccines, instances of Guillain-Barré syndrome observed in flu vaccine recipients in 1976, and the connection between narcolepsy and a specific flu vaccine in 2009. Against this backdrop, it is not surprising that so many medical and public health experts voiced concerns about covid mRNA vaccines bypassing the normal safety testing process. Concerns about inadequate safety testing extend beyond the usual regulatory approval standards and practices. As there were no specific regulations at the time of the rapid approval process, regulatory agencies quickly “adapted” the products, generalised the definition of “vaccine” to accommodate them, and then authorised them for EUA for the first time ever against a viral disease. Due to the GTPs’ reclassification as vaccines, none of their components have been thoroughly evaluated for safety. The main concern, in a nutshell, is that the covid mRNA products may transform body cells into viral protein factories that have no off-switch – i.e., no built-in mechanism to stop or regulate such proliferation – with the spike protein (“S-protein”) being generated for prolonged periods, causing chronic, systemic inflammation and immune dysfunction. When the S-protein enters the bloodstream and disseminates systemically, it may become a contributing factor to diverse AEs in susceptible people. Enforce a Global Moratorium Given the well-documented SAEs and unacceptable harm-to-reward ratio, we urge governments to endorse and enforce a global moratorium on these modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered. https://expose-news.com/2024/01/26/researchers-urge-a-global-moratorium-on-mrna/

Israel Accuses The ICJ Of (You Guessed It) Antisemitism Caitlin Johnstone Listen to a reading of this article (reading by Tim Foley): The International Court of Justice rejected Israel’s request to dismiss the genocide case brought against it by South Africa on Friday, ruling by a massive majority that the case shall proceed and instructing Israel to refrain from killing and harming Palestinians in the interim. Many Palestine supporters have expressed dismay that the ICJ did not explicitly order a ceasefire, while many others (including South African officials) argue that the ruling is very positive and tantamount to a ceasefire order because it demands the end of harm to members of the protected group. Imperial media are aggressively emphasising the absence of a ceasefire order in their headlines and many Israel apologists are framing that absence as a victory for their favorite ethnostate, but such performative chest-thumping is severely undercut by the way high-level Israeli officials are currently accusing the ICJ of antisemitism and saying Israel should ignore its rulings. https://twitter.com/guardian/status/1751048855032926448 “The international court of justice went above and beyond when it granted South Africa’s antisemitic request to discuss the claim of genocide in Gaza, and now refuses to reject the petition outright,” complained Israeli defense minister Yoav Gallant in response to the ruling. “The decision of the antisemitic court in The Hague proves what was already known: This court does not seek justice, but rather the persecution of Jewish people,” said Israeli national security minister Itamar Ben Gvir. Ben Gvir also tweeted “Hague Schmague” immediately after the ruling was issued, which will probably go down in history as the most Israeli tweet of all time. Everyone’s arguing about whether or not the ICJ’s ruling is helpful, and I don’t know enough one way or the other to be sure either way, but from where things stand right now it does seem unlikely to me that managers of the Israeli war machine would be getting this freaked out and whipping out their tired old “antisemitism” song and dance if there wasn’t something of substance to it. International lawyer Francis Boyle, who won provisional measures against Yugoslavia at the ICJ in 1993, said the following of the ruling: “This is a massive, overwhelming legal victory for the Republic of South Africa against Israel on behalf of the Palestinians. The U.N. General Assembly now can suspend Israel from participation in its activities as it did for South Africa and Yugoslavia. It can admit Palestine as a full member. And — especially since the International Criminal Court has been a farce — it can establish a tribunal to prosecute the highest level officials of the Israeli government, both civilian and military.” So take that for whatever that’s worth to you. In any case the butchery in Gaza still urgently needs to be ended, and only time will tell whether Friday’s development had any major effect on the outcome of this horror. But man what I wouldn’t have given to be a fly on the wall at the meetings they were having at the US State Department on Friday. It’s days like this that remind you why empire managers switched from talking about “international law” to using the meaningless phrase “rules-based international order”. ________________ My work is entirely reader-supported, so if you enjoyed this piece here are some options where you can toss some money into my tip jar if you want to. Go here to buy paperback editions of my writings from month to month. All my work is free to bootleg and use in any way, shape or form; republish it, translate it, use it on merchandise; whatever you want. The best way to make sure you see the stuff I publish is to subscribe to the mailing list on Substack, which will get you an email notification for everything I publish. All works co-authored with my husband Tim Foley. Bitcoin donations: 1Ac7PCQXoQoLA9Sh8fhAgiU3PHA2EX5Zm2 https://open.substack.com/pub/caitlinjohnstone/p/israel-accuses-the-icj-of-you-guessed?r=29hg4d&utm_medium=ios&utm_campaign=post

The Pfizer COVID-19 “vaccines” forced on humanity were not the same ones used in Pfizer’s clinical trials. There was a “bait-and-switch.” The public received vials contaminated with plasmid DNA. Florida Surgeon General Dr. Joseph Ladapo says there is “zero question” that the mRNA shots could change people’s DNA. Moreover, he said, “I think it’s probably likely that that is, in fact, happening.” https://x.com/vigilantfox/status/1747324110558896154?s=46

How to Fake Pandemics in 4 Easy Steps A masterclass by the DOD showman, James Giordano. Sasha Latypova Who here still believes covid was a real viral pandemic? Or even an epidemic? Welcome! We don’t judge! Actually we do - you are an idiot if after 4 years of this charade you still believe that was an epidemic. The data is clear that there was none, US Government/Trump announced “public health emergency” based on about 40 cases in China without any significant evidence of real illness or economic impact. State governors announced public health emergencies based on nothing. In Ohio it was 3 cases of covid that became the basis for shutting down the entire state. This is because declarations of public health emergency, by law, require no evidence that an emergency exists. Opinion of one unelected bureaucrat is all that’s needed. The US Government then provided massive funding to fake-PCR label “covid” cases and murder people in hospitals with remdesivir+vent protocols while denying early effective treatment, as well as fake PCR-attributing covid causes to anything including motor vehicle deaths and gun homicides. Coquin de Chien John Beaudoin is a great resource on learning about this fraud-and-murder event labeled as “pandemic”, and if you have not yet subscribed to his stack, I recommend you do so. Pandemics do not exist at all. They are not possible in nature. Had they been possible, we would not be here. At this point I am asked - but the plague! The smallpox! The cholera! The answer is - these are diseases related to lack of sanitation, crowding, infestation with rats and fleas, human and animal waste polluting the drinking water. Once these problems are addressed, epidemics do not exist. And these diseases never caused global pandemics anyway. The “Spanish flu” was also a fake pandemic, a narrative manufactured probably decades after. Pandemics are also not possible via “science” and what is called gain-of-function research which amounts to mostly ridiculous attempts at software enabled sorcery, making soups of chemicals mixed with literally shit, as I discussed in my previous article. Yes, toxic chemicals and shit can cause poisoning, but this does not spread by itself. Of course, these labs should be shut down as a waste of money and a local health hazard (mostly to those working in the labs). Big thanks to Meryl Nass for pointing to this important piece of data published by the Lancet: A new study reports 309 lab acquired infections and 16 pathogen lab escapes between 2000 and 2021, several deaths/ Bulletin of the Atomic Scientists https://www.thelancet.com/action/showPdf?pii=S2666-5247%2823%2900319-1 https://thebulletin.org/2023/12/a-new-study-reports-309-lab-acquired-infections-and-16-pathogen-lab-escapes-between-2000-and-2021/#post-heading The CDC collects about 200 reports per year of lab accidents, leaks, escaped infected animals or infected staff. So this report is a gross un… Read more 23 days ago · 160 likes · 64 comments · Meryl Nass I think the Lancet was trying to make the opposite point vs the one they actually made. The paper identified 51 scary pathogen “leaks” from labs worldwide (mostly in North America and China). Additionally, CDC collects reports of about 200 of these “escapes” a year in the US (so Lancet paper is a severe under-count of these potentially apocalyptic events). This many dangerous leaks of dangerous pathogens a year! We should have world ending catastrophes every week, right? Lancet says it did not result in anything like this… There were 8 deaths (bad and tragic, and in lab workers themselves), and many “exposures” (imaginary concept in public health to justify throwing political dissidents and other random people into quarantine camps). There was one incident in China where 10,000 people acquired bacterial infection. OK, that’s bad too, but did China lock down? Did Europe and US close all flights from China? How come with such large “outbreak” nothing travelled by air and killed half the world? I mean with the coof, the entire world locked down after 40 cases or so! Why, with seemingly plenty of opportunities for lab leaks, do pandemics happen only on command from the WHO? And only after all key countries practiced those exact pandemics numerous times in table top exercises? All pandemics to date have been faked by the military-industrial globalist cabal (with numerous witting and unwitting participants): Sorry, RFK Jr., despite your desire to appear middle ground by including a lie with a majority truthful statement, covid “pandemic” was also faked, using the same basic script, actors and funding. What is the pandemic script? Let’s hear it from the horse’s mouth. Here is a DOD showman James Giordano. He is not a real scientist, his business is spinning clickbait science propaganda. In this lecture he is explaining how to fake pandemics in four easy steps in a video from 2017 “Neurotechnology in National Defense”: Step 1: Poison a few people in a few geographic locations (“sentinel cases”) with a drug (chemical toxin or bio-toxin) that causes “highly morbid” central nervous system (CNS) effects . [I told you “covid” was a synthetic toxin, didn’t I?] Step 2: Pretend it was “a bug, a virus modified with CRISPR Cas9” (what James means here is - “oops, forget what I just told you 45 seconds ago about A DRUG. I really-really mean a bioengineered GOF virus!!”) Step 3: Use the “REAL BUG” - the Internet! Broadcast on social media that everyone is infected with a “highly lethal agent” that has “asymptomatic, prodromal effects” - anxiety, sleeplessness and worry. When you worry - those are the signs that you have a “lethal asymptomatic infection”. M-kay. That means the undergraduate students in a garage someplace released the bioweapon. Or it “leaked” from BSL4 facility in Wuhan (that sounds scarier, doesn’t it?), and it got to you all the way in Iowa. Believe!!! Step 4: All hypochondriacs and “worried-well” run to their doctors and flood the hospital ERs, yay! Now we can get them with the fake PCR-remdesivir-ventilator protocol! and call it “covid”! PS. For extra fun play a game of confusing messages and denial with CDC. Does this explain Fauci’s flip-flop on masks early on in 2020 - you bet it does! There is a “step 0” that’s required for this plan to really work out - that is constant brainwashing of the masses, programming their brains to respond to some key trigger words in a predictable fashion. Here is one such example (“Blacklist”, 2014): I think the 5th horseman is called “ScienceMAD” and he rides a Chimera, something like this: Chimera with a Male Andalusian horse and a face of a goose again Stock Image Now, let’s hear from the field operative, the real practitioner. Here is now famous Indiana Jones by name of Michael Callahan, the CIA agent with a cover of “infectious disease doctor” explaining his job very clearly. You see, his job is to make prophecies of what viruses with pandemic potential will “inevitably emerge” (wink wink) and then make “vaccines” for them almost immediately. I think it is clear that he is not a real scientist either, but a “prophet” of sorts. https://twitter.com/LivewithAndy/status/1701987736406675770 In a related post I discussed another cabal thespian whose amplua includes pretending to be an infectious disease doctor, too - Col Matt Hepburn, evangelizing the crowd at TED: "Pandemic Preparedness" - a Government Protection Racket "Pandemic Preparedness" - a Government Protection Racket Meet Col Matt Hepburn who in 2020 leads an effort for the Department of Defense called Enabling Technologies. Enabling Technologies rapidly develops new vaccines and treatments against future (!) infectious disease challenges. Matt can predict the future and “protect” you from it. Read full story This racket is so profitable that they are getting tired of coming up with names for their fake “novel viruses” and fake pandemics and are simply switching to “Disease X” here and here. Oh, and look at that - a new bill in Congress: Image Image I am also tiered of repeating how utterly stupid it is to “predict” vital pandemics, especially of “unknown but deadly nature”, so I am going to refer you to this good piece of writing explaining this nonsense. The X Files: A Primer on the Next Plandemic My recent or only-intermittent readers may not buy this, but I truly do try to be sympathetic to the people who fell (and continue to fall, bless their trusting little hearts) for the wickedest and most prolific propaganda campaign in history. I have attempted to exonerate or at least understand the medical professionals who—despite overwhelming, irrefu… Read more 3 days ago · 72 likes · 55 comments · Jenna McCarthy My own assessment of what Disease X means - the cabal has been and is planning to continue using chemical, biological, radiological and nuclear weapons (yes, CBRN weapons, all of them) on populations in increasing scale and variety. These are internationally prohibited activities that the criminals in US Government and other governments are engaged in by renaming them into “health events” and “preparedness”. Is this dangerous? Yes, just as any act of terrorism. However, we can really get prepared for their “preparedness” by dispelling their fake fear narratives of mutating invisible self-spreading bullshit, and staying alert, utilizing common sense, not relying on their murderous “healthcare” and helping each other. Art for today: Portrait of a young man, 14x18 in. https://sashalatypova.substack.com/p/how-to-fake-pandemics-in-4-easy-steps?utm_medium=ios

A summary of the evidence against the COVID vaccines Here's a quick summary of the key pieces of evidence that taken together show that the COVID vaccines are unsafe and that the medical community should not be trusted. Steve Kirsch What is evidence-based practice? Here is a short list of reasons that everyone should be concerned about the COVID vaccine. This is not an exhaustive list. Doctors are told to trust the FDA and CDC, but not verify, when prescribing vaccines. All the post-marketing safety data is kept hidden by health authorities so not even doctors can look at the data themselves to find out if any vaccine is safe. Doctors have to trust the authorities. They are essentially told: “trust, do not verify.” Zero Trust “Don't trust any, but verify, every time all the time.” The CDC itself doesn’t have the data to make a post-marketing independent vaccine safety assessment and they are not interested in obtaining the data either! The CDC relies on the FDA who relies on the manufacturer to test the product. The CDC could ask states for vaccination records tied to death records, but they don’t want to even ask because if they did an analysis, it could be discovered in a FOIA request. The CDC basically has no interest whatsoever in verifying what the actual safety data is. Lack of transparency by health authorities. Not a single health authority anywhere in the world has ever released anonymized record-level patient data for independent researchers to assess the safety of any vaccine. There isn’t any paper in a peer-reviewed journal showing that health outcomes are improved if public health data is kept secret. Lack of interest in data transparency by the medical community. Can you name a single high-profile pro-vaccine member of the medical community who has called for data transparency of public health data? Time-series cohort analyses can be easily produced by health authorities and published for everyone to see. These would show safety signals and do not jeopardize patient privacy. These are all kept hidden. We aren’t allowed to see even the simplest of charts. Wouldn’t it be great to define two cohorts on July 1, 2021: COVID vaccinated vs. COVID unvaccinated. Then you simply record the deaths from that point forward and plot them. Why isn’t this being published? Misinformation is deemed to be a problem, but the people making these statements are unwilling to take any steps to stop the so-called misinformation. These steps include: open public discussion to resolve differences of opinion and making public health data available/public in a way that preserves privacy. For example, HHS (as well as every state health department) should welcome all of us with open arms and invite us to query their databases (such as VSD and Medicare in the case of HHS) and publish whatever we find. Why does this information need to be hidden? The numbers tell the story, not the individual records. No response from health authorities to reasonable requests. I’ve sent emails to Sarah Caul of the UK ONS on four ways the ONS can increase data transparency. There was no response. No response when asked to explain damaging evidence. When credible scientists receive government data that shows very troubling safety signals, there is a total unwillingness of any health authority to discuss the matter and resolve it. The US Medicare data clearly shows mortality increases after people take the jab. Is there any epidemiologist who can explain why deaths rose during a period in time when they should have been falling (per the Medicare death data)? For the first 120 days after the shots given in March 2021, death rates overall were falling. But if you got the vaccine, your death rates went up. We know from data from other vaccines that the baseline death rate of 81-year olds in Medicare is 3.85%, so the baseline death rate of this group is <800 deaths a day. These deaths climb far above baseline after you took the COVID shot. The patient-level data released from NZ data confirms that mortality increases after the shots are given despite the fact that most of the shots were given during time periods when deaths were falling NZ data: Doses 2 and 4 were given while background mortality was falling, dose 3 while rising. So we’d expect the slope to fall in the first 6 months after vaccination. It does the opposite. Anecdotes such as the one from Jay Bonnar who lost 15 of his DIRECT friends unexpectedly since the shots rolled out. Four of the 15 died on the same day as that vaccine was given. Before the shots rolled out, Jay had lost only one friend unexpectedly. The probability this happened by chance is given by poisson.sf(14, .25) which is 5.6e-22. So this can’t happen by chance. SOMETHING killed Jay’s friends and 4 of the 15 died on the same day as they were vaccinated. Is there a more plausible explanation for what killed Jay’s friends? All of them who died were vaccinated with the COVID vaccines. Well done studies like the one done by Denis Rancourt showing 1 death per 800 shots on average. Jay Bonnar estimates he has around 14,000 friends so Jay’s numbers are consistent with Rancourt’s results. Survey data like Skidmore and Rasmussen Reports showing that hundreds of thousands of Americans have been killed by the COVID shots. There have never been any counter surveys published showing this not to be the case. The lack of any success stories. It appears that “vaccine success stories” where COVID infection fatality ratios dropped or that myocarditis cases plummeted do not exist. The US Nursing home data shows that the infection fatality rate (IFR) increased after the vaccine rolled out. There is nobody using that data making the claim it reduced the IFR. Anecdotes from healthcare are extremely troubling. One nurse reported a hospital admission rate that was 3X higher than anything in the 33-year history of the hospital after the COVID vaccines rolled out. Symptoms rarely ever seen were common after vaccines rolled out in that age group. Lack of autopsies in clinical trials and post-marketing. The CDC doesn’t request anyone to do autopsies even for people who die on the same day as they got the vaccine. Don’t they want to know what killed those people… just to be sure? Young people dying in sleep. There are way too many cases of young people who die in their sleep after being vaccinated. Doctors say this is a rare event. Now it is much more common. If the shots are safe, why is this happening? I have direct personal experience with the vaccine: two people I know were killed by the vaccine, none from COVID. I know many people who are vaccine injured from the COVID vaccine. Corruption in the VAERS system used to track adverse events. See this presentation by Albert Albert Benavides. In addition, the v-safe system showed that 8% of the people who got the vaccine had to see medical attention (which is in itself a train wreck), but the CDC refused to voluntarily disclose this important information and even today they don’t talk about it. The CDC covered up 770 safety signals. They didn’t tell the public about them at all. Not even hinting at them. A safety signal is very serious. To get one safety signal would be concerning. But to get 770 safety signals triggered (on 770 different adverse event types) and then not say anything to the public about it is a sure sign of a very corrupt public agency whose job is to protect the manufacturers, not the public. Ed Dowd’s book statistics. This very popular book (“Cause Unknown”) listed 500 who died unexpectedly. Ed didn’t know how many were unvaccinated. Only one person has come forward saying that one of the people in the book who died after the vaccines rolled out was unvaccinated. Prominent doctor/scientists switching sides. Paul Marik is one of the top intensivists in the world. After seeing many COVID vaccine injured patients, he changed his mind about the safety of vaccines. When he was not allowed to practice medicine consistent with his Hippocratic Oath, he resigned his position. The corruption with COVID protocols. The COVID hospital protocols likely caused 90% of the COVID deaths in hospitals. This led to Paul Marik resigning. See details in this article. Why are doctors forced to use hospital protocols that kill a huge percentage of patients instead of using their best judgment to save patients? This JAMA paper shows that COVID and influenza vaccines don’t work. Why are we pushing a vaccine where the statistics clearly show the vaccines don’t work? The consistency of the data. There have been no counter-anecdotes showing the vaccines are safe. I keep looking for one and come up empty. No debates with anyone prominent promoting the government narrative. Those who promote the narrative refuse to engage in any scientific discussions to resolve differences of opinion. This is similar to the question of whether vaccines cause autism: nobody who thinks it doesn’t is willing to engage in a public discussion about it to discuss the evidence. Why not resolve the issue through dialog? It isn’t resolved in the peer-review literature where half the papers say vaccines cause autism and the other half don’t. Why can’t we talk about it? Fear and intimidation tactics are used to silence dissent. Open debate would be more productive. But people are not allowed to hold or discuss views that go against the “consensus” or they will lose their jobs, their certifications, or their medical licenses. Health care workers are told they will be fired if they report an adverse event to VAERS, there are nurses who won’t talk about anaphylaxis after getting the vaccine for fear of being fired, vaccine injuries are covered up, hospital workers are afraid to talk about it at work. The cognitive dissonance is very disturbing. When healthcare workers bring up the topic of mortality and morbidity due to the vaccine, their peers say nothing and walk away. Censorship tactics employed by the US government to silence dissent instead of public recorded open debates. History has shown that purveyors of censorship are always on the wrong side of the issue. Liberty Justice Center Wins Battle for Doctors' First Amendment Rights as California Repeals Physician Censorship Law - Liberty Justice Center https://open.substack.com/pub/stevekirsch/p/a-summary-of-the-evidence-against?r=29hg4d&utm_medium=ios&utm_campaign=post

The article discusses concerns that contamination in the COVID-19 mRNA vaccines, specifically residual DNA from the manufacturing process, could help explain the recent rise in cancer rates and autoimmune diseases. Pathologist Dr. Ryan Cole explains that while the initial Pfizer vaccine trials used a very controlled synthetic mRNA production process, when they scaled up manufacturing for billions of doses they switched to a less precise method involving bacteria and plasmids, without properly cleaning the residual DNA. He and other experts believe this contaminated DNA could be intercalating into human DNA and causing mutations, suppressing the immune system, and driving cancers that are more aggressive and no longer responding to traditional treatments. More research is still needed, but this provides a potential mechanism for the alarming patterns doctors are observing of rapid cancer growth and previously stable cancers coming out of remission after vaccination. https://www.theepochtimes.com/us/the-rise-in-cancers-autoimmune-diseases-the-role-of-dna-contamination-5544587 No paywall source: https://archive.is/G0Shq The Rise in Cancers, Autoimmune Diseases: The Role of DNA Contamination The Rise in Cancers, Autoimmune Diseases: The Role of DNA Contamination Pathologist Dr. Ryan Cole in Dallas, Texas on Nov. 4, 2023. (York Du/The Epoch Times) In a recent episode of “American Thought Leaders,” host Jan Jekielek speaks with Dr. Ryan Cole, a pathologist and an expert on SARS-CoV-2 and the mechanisms of the genetic injections labeled as vaccines. Here, they discuss how these COVID-19 genetic vaccines may be related to the rise in cancers and autoimmune diseases. Jan Jekielek: I’ve done an interview with Kevin McKernan about what’s in the vaccine vials, this contamination that multiple labs had already verified. Let’s start with that, because that’s something you’ve been covering. Dr. Ryan Cole: Many laboratories around the world have been looking at this issue, and Kevin has been a leader in this area. When these products were made, there was the J&J, that’s an adenovirus factor, but then there was Moderna and Pfizer. These are mRNA; synthetically engineered, modified RNA. For the trials, at least for Pfizer, there’s a synthetic PCR-type process in making up the mRNA sequence for these shots. That was given to 40,000 people, and was a deliberate, synthetic, engineered attempt at a precision-type process. Mr. Jekielek: That’s dubbed “Process 1”? Dr. Cole: Yes. To make a lot of this for billions of people, a second process was used, which was only tested on about 252 people instead of 40,000. That was taking this complementary DNA sequence that is the reverse pattern of the spike to make mRNA a message, and then your body would make that protein in your cells. We did the trials on this very controlled synthetic process, but then at the last minute they snuck under the radar and said, “But we’re going to make all the rest of them using a process we’ve barely tested.” That’s what got rolled out into billions of people’s arms. It was kind of a bait and switch. Those large data sets one would want to see in terms of harms, you’re not going to find that in 250 patients. Mr. Jekielek: They actually use E. Coli, a bacterium, to grow these plasmids of DNA, which can then be turned into the RNA, but they just didn’t clean them up. Dr. Cole: They didn’t clean them up properly. They’re supposed to put in an enzyme that breaks down any residual DNA. Even up to the current vials of the fall booster, the XBB 1.5, Kevin and 12 other laboratories have shown there is still bacterial plasmid DNA contamination within these vials. The FDA allows up to, in gene products, 10 nanograms of DNA per dose, but that’s based on old technology. The smaller the fragment of DNA, the greater the opportunity it has to intercalate into your own DNA as well. More testing and probes are still needed to prove this, but it explains a lot of the strange happenings we’re seeing in clots, autoimmune disease, and cancers, because we’re changing signals within cells. Human cells are meant to make human proteins. They’re not meant to make foreign proteins. When we program people’s cells to make things they’re not supposed to make, they can go haywire. They can mutate and become a target of our own immune system. My big concern is that billions of people around the world have received a product that was contaminated, which was admitted to by the Canadian health regulatory agency. Mr. Jekielek: It was Epoch Times reporting that caused that disclosure to happen. Dr. Cole: Yes, well done. And my concern isn’t just these COVID shots. It’s this entire technology. A lipid nanoparticle in and of itself is an unproven product. It takes on whatever you put into it. They’re trying to create them for RSV, flu, and for many other pathogens. It still takes those little gene sequences anywhere and everywhere in the body. In some of his autopsy findings, the late Dr. Burkhardt, a friend and mentor to me, showed spike protein in the testes, in the placenta, and in the uterus. I’ve seen some of those in the studies we were doing in my laboratory. Mr. Jekielek: You feel this provides some explanation for these turbo cancers and this clotting we’ve been seeing. Dr. Cole: Dr. Ute Krüger from Sweden coined the term turbo cancer. She’s a breast pathologist who was looking at the damage of these shots. She noticed increases in cancer, an uptick not only in the size of the cancers, but also in the stage of the cancers. Instead of just taking out a lesion, she was finding it had spread to lymph nodes, the liver, the bone marrow, and the brain. She was seeing cancers behave in a manner like never before. Everywhere I go, I hear oncologists and physicians telling this story. A prominent oncologist in Texas told me, “At first I saw the clots, then the blood cancers, the leukemias, and the lymphomas. Now, I’m seeing solid tissue cancers at rates I’ve never seen. Patients that were stable or cancer-free for 1, 2, 5, or 10 years, their cancer is now back, and it’s not responding to traditional therapies.” It’s not necessarily that the gene sequence is causing cancer. The gene sequence can cause some of the mutations that lead to cancer. But it’s also suppressing the immune system, and your immune system is what kills cancer. If your immune system is asleep, your killer cells can’t be activated In addition, there are so many basic things our public health system isn’t addressing. Do we have a horrible diet? Are we vitamin D-deficient? Absolutely. In addition, a lot of people received a contaminated adulterated gene-based product, and we don’t know the long-term outcomes. Mr. Jekielek: Ryan, any final thoughts as we finish up? Dr. Cole: If we can resolve conflicts by having face-to-face conversations, the world will be a better place, and maintaining our rights to speak and think freely is more important than anything. Stay positive. Stay optimistic. Life is still good. This interview has been edited for clarity and brevity.