5 Emerging Technologies that Could Destroy the World
BY : GLYN TAYLOR July 7, 2013
5 technologies that could destroy the world
Through the accelerating rate of our technological advancements, we are now seeing the rise of revolutionary new technologies. Even from an optimistic perspective, many potential threats can be foreseen. These are our proposed top 5.

In the book ‘Our Final Century: will the human race survive the twenty-first century?‘, Martin Rees concludes that humanity has just a 50/50 chance of surviving the 21st century. We refrain from applying such odds, as the century is fraught with unpredictability and even incomprehensibility. Certain future events though are certain to happen, should growth continue uninterrupted.

Medical Nanobots
Medical Nanobots
1 & 2 – Nanotechnology & 3D Printers

Nanotechnology describes a wide variety of technologies and materials that share one thing in common: They are incredibly small in size. Typical nanostructures are the width of a strand of DNA (2 nanometers), 50 thousand times smaller than the width of a strand of hair. We are already seeing the emergence of nanotechnology; you can read about that in our article, ‘Phase One of the Nanotechnology Revolution has Begun‘. Nanotechnology will really start to make an impact on our world in the next couple of decades; you can read about that in our article, ‘Superhumans Created by Nanotechnology within 30 years‘. For more general background information about nanotechnology, visit here.

Why we need nanotechnology

Growth of Nanotechnology

Just as the industrial revolution ushered our way into the world we know today, nanotechnology will soon change our world beyond comprehension. It is predicted to cure all current types of illness, even aging. It will lead to massive improvements in battery and solar power, ending our dependence on the Earth’s gas, coal, and oil resources. Nano Fabricators will allow us, in our homes, to 3D-Print anything by literally building it from scratch. Quantum computing will create computers that are billions of times more powerful than the ones we have today. Many many more innovative examples exist; literally everything you know will be dramatically enhanced by nanotechnology.

But how it could destroy us

Yes, but the risk of misuse of these breakthroughs rises along with the benefits. There are many potential threats that could be caused through nanotechnology misuse/accident, of which provide an existential risk (a risk that would either annihilate Earth-originating intelligent life or permanently and drastically curtail its potential).

The Blood Brain Barrier
The Blood Brain Barrier
One of the soonest and simplest threats could arise from the ability of ‘passive’ nanostructures to pass through the blood-brain barrier. This barrier is a tightly knit layer of cells that affords the brain the highest possible protection from the simple chemicals and microorganisms that could harm it. Neuroscientists are purposefully engineering nanoparticles that can cross the blood-brain barrier to deliver medicines in a targeted and controlled way directly to diseased parts of the brain. This ability would also be utilised by the malevolent, in the creation of new forms of biological and chemical weaponry. These types of new biological/chemical WMDs would utilise simple non-toxic chemicals (which would harm the brain but not anything else), which would consequently be very hard to detect by authorities. At its simple stages though it is unlikely to cause an existential risk as it would not be contagious. Further advances though will see the rise of ‘active’ nanostructures, which pose a far greater threat. These are essentially nano-sized robots, which can be programmed to perform specific tasks. Tasks could be to attack certain materials, such as metals, water, internal organs, or specific DNA sequences.

Apocalyptic Scenario 1: Human Killing Nanobots

NanobotsActive nanostructures (nanobots) can be programmed to specifically target and kill humans. The smallest insect is about 200 microns; this creates a plausible size estimate for a nanotech-built antipersonnel weapon capable of seeking and injecting toxin into unprotected humans. The human lethal dose of botulism toxin is about 100 nanograms, or about 1/100 the volume of the weapon. As many as 50 billion toxin-carrying devices—theoretically enough to kill every human on earth—could be packed into a single suitcase. You can read more about this threat, here.

A potential exists that the activity of anti-technology terrorists would significantly increase in the future. This could be in response to the imminent development of an Artificial General Intelligence, which the anti-technologists may believe could turn against humanity. They may see it as necessary to release the ‘human killing nanobots’, to prevent an AGI from rising. They could create the nanobots using advanced molecular 3D-Printers, which by the 2040’s will be owned by many production companies, universities and research centers. Eventually, such printers will be available in all homes.

Apocalyptic Scenario 2: Gray Goo

Another threat of nanobots could arise from the Gray Goo Problem. Gray Goo is easily defined and explained as, ‘runaway nanobots’: A swarm of rapidly self-replicating nanobots, in a ravenous quest for fuel, which would consume the entire biosphere until nothing remained but an immense, sludge like robotic mass. It is incredibly difficult to build though, and so an accidental release will be very unlikely. As time passes though it will become easier to build, and if regulation is not put in place to allow it to be detected & disabled, then a terrorist organisation could release it. You can read more about the Gray Goo Problem, here.

3 & 4 – Artificial General Intelligence & Big Data

AGI is defined as a ‘conscious’ artificial construct that would be an intellectually independent thinker, just as are humans. It is predicted by Ray Kurzweil (Chief of Engineering at Google) and many others, that the first AGI will be operational before 2030. For more information about the basics of AGI, visit here.

Big Data is what we are creating through our use of social networks and smartphone apps. The data pot will become so immense that it can be assembled by us and utilised in new apps which have the new capability of understanding us and our world. Google could use the date to not only respond accurately to your search requests, but preempt what those requests will be. Big Data will drive forward a world where everything is connected in what is called the ‘Internet of Things‘. Our world will become ‘smart’, and that will give AGI a far better understanding, and potential control.

Why we need Artificial General Intelligence

When we develop an AGI that is significantly more intelligent than human beings, our rate of evolution will rapidly accelerate. The world which would as consequence be created, is mostly incomprehensible. The level of the resulting technological advance and incomprehensibility, has been referred to as the ‘Technological Singularity‘ (an event horizon that cannot be predicted beyond). What we hope though is that it will define the next stage of our evolution; we will transcend our biology; our Earth bound reality will only be the beginning; we can explore the universe; explore our existence; our creator; we can become the creator; become Gods.

But how it could destroy us

Optimistically, our future is a wondrous one. The reality though is fraught with security concerns. The main concern with AGI arises from what we have all seen in the movies – our machines turning against us. The University of Cambridge has launched a Centre for the Study of Existential Risk, which has the primary task of studying AGI risk.

The exact development strategy of AGI is largely as yet unknown. It could involve the integration of an already adult, human mind (as will be seen in the 2014 Johnny Depp movie, Transcendence); it could involve an artificial mind being activated, which would learn from scratch, just as a human child would; or it could be a supercomputer that is tweaked by adding hardware that would allow it to become conscious.

Apocalyptic Scenario 3 – The Terminators

Terminator ScenarioA potential threat is if the AGI has limited capacity to think intellectually (Weak AI). The threat of this has already been seen in humans. It translates as small mindedness, or selfishness. An example of a small minded group would be Al-Qaeda; it’s members have shown an incapability of thinking about other possibilities; they believe their religion is all that matters. As consequence, it is not possible to reason with them, no matter how intelligent they are; they believe they are morally superior.

If an Artificial Intelligence was to be ‘small minded’, it would be against all views which are not inline with its own, even if other opinions are rationally more likely to be correct. It would see all other ideologies as a threat. If humanity as a whole is in disagreement with it, possibility arises for a war of which we would be striped of our technological advantage, or made extinct. Big Data will allow this rogue Weak AI to potentially take control of all we know with the unleashing of a ‘superbug’, taking our cars, home appliances, power stations, communications, weapons etc; plummeting humanity back into the dark ages, or killing us off altogether.


Biotechnology5 – Biotechnology

The term biotechnology is used to define “any technological application that uses biological systems, living organisms or derivatives thereof, to make or modify products or processes for specific use” (Definition by UN Convention on Biological Diversity). Depending on the tools and applications, the term often overlaps/encompasases the fields of biomedical engineering, tissue engineering, biopharmaceutical engineering, genetic engineering, chemical engineering, bioprocess engineering, bioinformatics (a new brand of information technology), and biorobotics. Biotechnology is also researched and developed at the nanoscale, and so may also be spoken of as being a nanotechnology.

Why we need biotechnology

As obvious through the amount of biotechnology fields, it is set to make a huge impact on the world. Most exciting is the impact it will have on health care. Genetic therapy is currently being used to create cures for diseases such as cystic fibrosis, AIDS and cancer. And to go beyond exciting, into what most consider is not even possible, it is believed that developments in telomerase gene therapy could lead to effective indefinite lifespans. Visit the website of the SENS Foundation to see how humanity could bioengineer its immortality. You can read more about immortality on our website, here.

But how it could destroy us

With the ability to reengineer our own biology, comes the ability to easily destroy it. The Cambridge Project for Existential Risk cites that, “because the seriousness of these risks is difficult to assess, that in itself seems a cause for concern”. The reality is that any imaginable disease could be potentially created.

Bio WeaponsThe most dangerous examples are engineered diseases that are contagious, airborne, have long life spans and are able to avoid antibiotic attack. These new diseases could target anything their creator wishes, for example: The reproductive organs, destroying humanities ability to reproduce; organisms which have short telomere lengths – only killing people above a certain age; the eyes, blinding everybody; only certain ethnic groups, or a certain gender. It could be used to change our genetics, perhaps even transforming the science-fiction into reality with the creation what could be considered as Zombies.

Current biological weapons are simple organisms that have been produced through natural growth, and not genetically modified through gene therapy. The upcoming phase of bioweaponry will feature organisms that have had their genes manipulated, giving them new pathogenic characteristics (increased survivability, infectivity, virulence, stealthy dormancy, drug resistance, etc). Bioengineering of the aforementioned type is grouped and referred to as ‘black biology’, or ‘Chimeras’.

Apocalyptic Scenario 4: Jihad Chimera

Some scientists predict that within 20 years, biotech research will have advanced to a great enough level to allow biologists to switch their talents to black biology, and with relative ease create advanced Chimera pathogens that are resistant to biological defences (antibiotics and known antidotes). Reasons for biologist to want to do this in the future are many. In this scenario, we will feature Islamic fundamentalists in a hypothetical future where their ideology has almost been eradicated.

The year is 2035, the majority of the world has been democratised and all but 1 country refuses to tolerates Islamist elements in their Governments; people want to be led by democratic governments who do not hold religious/ethnic bias. Iran is that 1 country, and has kept it’s religious rule; it has became ‘the last stand’ for violent radical Islamists who have flocked there for defence, because of the lingering public majority support for Islamist rule. The country had been defended from international sanctions by Russia and China, on the basis of ‘not interfering in other countries affairs’.

Next Phase of Bio Weapons

However, it becomes no longer in the Chinese and Russian interests to continue to defend Islamist Iran. Iran is left alone and living conditions in the country rapidly deteriorate. Iranians revolt against their leadership in desperation. Radical Islam now faces its final demise, as does the long ruling extremist regime.

In anticipation of this, the regime had been running a black biology programme in their planning for a final Jihad. A new Chimera pathogen has been developed (we will call it the Jihad Chimera).

In 2025, gene therapy had led to a complete cure for cancer. Everybody in the world had been vaccinated. The vaccine involved the addition of certain genes into the human genome.

The Jihad Chimera works by seeking out the cancer-inhibiting gene. It sits on the gene, deactivating it, and it works as a carcinogen, making it certain that infected people will, within a few years, develop cancer. Once cancer cells develop, it activates the Jihad Chimera, releasing toxins which in turn accelerate the rate of cancer growth, making the cancer again untreatable and far more aggressive than traditional cancers.

The Jihad Chimera is released by the Iranians throughout the world in 2035. It is even more infectious that the common cold and by 2036, all of humanity is silently infected. By 2037 the cancer pandemic begins. Attempts at developing cures are made, but by 2040 everybody has terminal cancer.



Question Mark

What do you think?

However unlikely the above apocalyptic scenarios are, the technological threats will be increasing. It is up to us now to avoid these scenarios and all other potential threats that could arise from our rapidly accelerating technological advances. The answer is not the banning of technological advance (as some have proposed), the answer is strict regulation and surveillance. The regulation does not have to slow down progress, neither does the surveillance have to encroach on our liberties. What they both need to do though is keep dangerous tech out of the hands of the malevolent. Our defence will be powered by our advancing tech. Our threats will be powered by… What do you think?



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Posted in Artificial Intelligence, Nanotechnology and tagged Active Nanostructures, Big Data, Cancer Treatment, Existential Risk, Immortality, Passive Nanostructures, Ray Kurzweil, Religion, The Singularity, Transcendence Movie 2014

5 Emerging Technologies that Could Destroy the World
BY : GLYN TAYLOR July 7, 2013
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mRNA Technology Gave Us the First COVID-19 Vaccines. It Could Also Upend the Drug Industry

BioNTech co-founders Dr. Ugur Sahin and Dr. Ozlem Tureci in its headquarters in Germany on Jan. 3. Photograph by Dina Litovsky—Redux for TIMEBY WALTER ISAACSONJANUARY 11, 2021 5:10 AM EST

“No!” The doctor snapped. “Look at me!”

I had been staring her in the eyes, as she had ordered, but when a doctor on my other side began jabbing me with a needle, I started to turn my head. “Don’t look at it,” the first doctor said. I obeyed.

This was in early August in New Orleans, where I had signed up to be a participant in the clinical trial for the Pfizer-BioNTech COVID-19 vaccine. It was a blind study, which meant I was not supposed to know whether I had gotten the placebo or the real vaccine. I asked the doctor if I would really been able to tell by looking at the syringe. “Probably not,” she answered, “but we want to be careful. This is very important to get right.”https://f0038f2a34d76ebd774c6dfa86a4f077.safeframe.googlesyndication.com/safeframe/1-0-38/html/container.html?n=0

I became a vaccine guinea pig because, in addition to wanting to be useful, I had a deep interest in the wondrous new roles now being played by RNA, the genetic material that is at the heart of new types of vaccines, cancer treatments and gene-editing tools. I was writing a book on the Berkeley biochemist Jennifer Doudna. She was a pioneer in determining the structure of RNA, which helped her and her doctoral adviser figure out how it could be the origin of all life on this planet. Then she and a colleague invented an RNA-guided gene-editing tool, which won them the 2020 Nobel Prize in Chemistry.

The tool is based on a system that bacteria use to fight viruses. Bacteria develop clustered repeated sequences in their DNA, known as CRISPRs, that can remember dangerous viruses and then deploy RNA-guided scissors to destroy them. In other words, it’s an immune system that can adapt itself to fight each new wave of viruses—just what we humans need. Now, with the recently approved Pfizer-BioNTech vaccine and a similar one from Moderna being slowly rolled out across the U.S. and Europe, RNA has been deployed to make a whole new type of vaccine that will, when it reaches enough people, change the course of the pandemic.

Drs. Ugur Sahin and Ozlem Tureci, Co-founders, BioNTech. In January 2020, before many in the Western world were paying attention to a new virus spreading in China, Dr. Ugur Sahin was convinced it would spur a pandemic. Sahin, who in 2008 co-founded the German biotech company BioNTech with his wife Dr. Ozlem Tureci, went to work on a vaccine and by March called his contact at Pfizer, a much larger pharmaceutical company with which BioNTech had previously worked on an influenza vaccine using mRNA. Less than a year later, the Pfizer-BioNTech COVID-19 vaccine became the first ever mRNA vaccine available for widespread use. Even so, Sahin, BioNTech’s CEO, and Tureci, its chief medical officer, maintain that BioNTech is not an mRNA company but rather an immunotherapy company. Much of the couple’s work—both at BioNTech and at their previous venture, Ganymed—has focused on treating cancer. But it is mRNA, and the COVID-19 vaccine made possible by the technology, that has pushed the famously hardworking couple into the ­limelight—and helped them become one of the richest pairs in Germany, though they reportedly still bicycle to work and live in a modest apartment near their office. Dina Litovsky—Redux for TIME

Up until last year, vaccines had not changed very much, at least in concept, for more than two centuries. Most have been modeled on the discovery made in 1796 by the English doctor Edward Jenner, who noticed that many milkmaids were immune to smallpox. They had all been infected by a form of pox that afflicts cows but is relatively harmless to humans, and Jenner surmised that the cowpox had given them immunity to smallpox. So he took some pus from a cowpox blister, rubbed it into scratches he made in the arm of his gardener’s 8-year-old son and then (this was in the days before bioethics panels) exposed the kid to smallpox. He didn’t become ill.

Before then, inoculations were done by giving patients a small dose of the actual smallpox virus, hoping that they would get a mild case and then be immune. Jenner’s great advance was to use a related but relatively harmless virus. Ever since, vaccinations have been based on the idea of exposing a patient to a safe facsimile of a dangerous virus or other germ. This is intended to kick the person’s adaptive immune system into gear. When it works, the body produces antibodies that will, sometimes for many years, fend off any infection if the real germ attacks.https://d-17721611131985076948.ampproject.net/2203041950000/frame.html

One approach is to inject a safely weakened version of the virus. These can be good teachers, because they look very much like the real thing. The body responds by making antibodies for fighting them, and the immunity can last a lifetime. Albert Sabin used this approach for the oral polio vaccine in the 1950s, and that’s the way we now fend off measles, mumps, rubella and chicken pox.

At the same time Sabin was trying to develop a vaccine based on a weakened polio virus, Jonas Salk succeeded with a safer approach: using a killed or inactivated virus. This type of vaccine can still teach a person’s immune system how to fight off the live virus but is less likely to cause serious side effects. Two Chinese companies, Sinopharm and Sinovac, have used this approach to develop vaccines for COVID-19 that are now in limited use in China, the UAE and Indonesia.

Another traditional approach is to inject a subunit of the virus, such as one of the proteins that are on the virus’s coat. The immune system will then remember these, allowing the body to mount a quick and robust response when it encounters the actual virus. The vaccine against the hepatitis B virus, for example, works this way. Using only a fragment of the virus means that they are safer to inject into a patient and easier to produce, but they are often not as good at producing long-term immunity. The Maryland-based biotech Novavax is in late-stage clinical trials for a COVID-19 vaccine using this approach, and it is the basis for one of the two vaccines already being rolled out in Russia.

The plague year of 2020 will be remembered as the time when these traditional vaccines were supplanted by something fundamentally new: genetic vaccines, which deliver a gene or piece of genetic code into human cells. The genetic instructions then cause the cells to produce, on their own, safe components of the target virus in order to stimulate the patient’s immune system.

For SARS-CoV-2—the virus that causes COVID-19—the target component is its spike protein, which studs the outer envelope of the virus and enables it to infiltrate human cells. One method for doing this is by inserting the desired gene, using a technique known as recombinant DNA, into a harmless virus that can deliver the gene into human cells. To make a COVID vaccine, a gene that contains instructions for building part of a coronavirus spike protein is edited into the DNA of a weakened virus like an adenovirus, which can cause the common cold. The idea is that the re-engineered adenovirus will worm its way into human cells, where the new gene will cause the cells to make lots of these spike proteins. As a result, the person’s immune system will be primed to respond rapidly if the real coronavirus strikes.https://f0038f2a34d76ebd774c6dfa86a4f077.safeframe.googlesyndication.com/safeframe/1-0-38/html/container.html?n=0

This approach led to one of the earliest COVID vaccine candidates, developed at the aptly named Jenner Institute of the University of Oxford. Scientists there engineered the spike-protein gene into an adenovirus that causes the common cold in chimpanzees, but is relatively harmless in humans.

The lead researcher at Oxford is Sarah Gilbert. She worked on developing a vaccine for Middle East respiratory syndrome (MERS) using the same chimp adenovirus. That epidemic waned before her vaccine could be deployed, but it gave her a head start when COVID-19 struck. She already knew that the chimp adenovirus had successfully delivered into humans the gene for the spike protein of MERS. As soon as the Chinese published the genetic sequence of the new coronavirus in January 2020, she began engineering its spike-protein gene into the chimp virus, waking each day at 4 a.m.

Her 21-year-old triplets, all of whom were studying biochemistry, volunteered to be early testers, getting the vaccine and seeing if they developed the desired antibodies. (They did.) Trials in monkeys conducted at a Montana primate center in March also produced promising results.

Bill Gates, whose foundation provided much of the funding, pushed Oxford to team up with a major company that could test, manufacture and distribute the vaccine. So Oxford forged a partnership with AstraZeneca, the British-Swedish pharmaceutical company. Unfortunately, the clinical trials turned out to be sloppy, with the wrong doses given to some participants, which led to delays. Britain authorized it for emergency use at the end of December, and the U.S. is likely to do so in the next two months.

Johnson & Johnson is testing a similar vaccine that uses a human adenovirus, rather than a chimpanzee one, as the delivery mechanism to carry a gene that codes for making part of the spike protein. It’s a method that has shown promise in the past, but it could have the disadvantage that humans who have already been exposed to that adenovirus may have some immunity to it. Results from its clinical trial are expected later this month.

In addition, two other vaccines based on genetically engineered adenoviruses are now in limited distribution: one made by CanSino Biologics and being used on the military in China and another named Sputnik V from the Russian ministry of health.https://f0038f2a34d76ebd774c6dfa86a4f077.safeframe.googlesyndication.com/safeframe/1-0-38/html/container.html?n=0

There is another way to get genetic material into a human cell and cause it to produce the components of a dangerous virus, such as the spike proteins, that can stimulate the immune system. Instead of engineering the gene for the component into an adenovirus, you can simply inject the genetic code for the component into humans as DNA or RNA.

Let’s start with DNA vaccines. Researchers at Inovio Pharmaceuticals and a handful of other companies in 2020 created a little circle of DNA that coded for parts of the coronavirus spike protein. The idea was that if it could get inside the nucleus of a cell, the DNA could very efficiently churn out instructions for the production of the spike-protein parts, which serve to train the immune system to react to the real thing.

The big challenge facing a DNA vaccine is delivery. How can you get the little ring of DNA not only into a human cell but into the nucleus of the cell? Injecting a lot of the DNA vaccine into a patient’s arm will cause some of the DNA to get into cells, but it’s not very efficient.

Some of the developers of DNA vaccines, including Inovio, tried to facilitate the delivery into human cells through a method called electroporation, which delivers electrical shock pulses to the patient at the site of the injection. That opens pores in the cell membranes and allows the DNA to get in. The electric pulse guns have lots of tiny needles and are unnerving to behold. It’s not hard to see why this technique is unpopular, especially with those on the receiving end. So far, no easy and reliable delivery mechanism has been developed for getting DNA vaccines into the nucleus of human cells.

That leads us to the molecule that has proven victorious in the COVID vaccine race and deserves the title of TIME magazine’s Molecule of the Year: RNA. Its sibling DNA is more famous. But like many famous siblings, DNA doesn’t do much work. It mainly stays bunkered down in the nucleus of our cells, protecting the information it encodes. RNA, on the other hand, actually goes out and gets things done. The genes encoded by our DNA are transcribed into snippets of RNA that venture out from the nucleus of our cells into the protein-manufacturing region. There, this messenger RNA (mRNA) oversees the assembly of the specified protein. In other words, instead of just sitting at home curating information, it makes real products.null

Scientists including Sydney Brenner at Cambridge and James Watson at Harvard first identified and isolated mRNA molecules in 1961. But it was hard to harness them to do our bidding, because the body’s immune system often destroyed the mRNA that researchers engineered and attempted to introduce into the body. Then in 2005, a pair of researchers at the University of Pennsylvania, Katalin Kariko and Drew Weissman, showed how to tweak a synthetic mRNA molecule so it could get into human cells without being attacked by the body’s immune system.

Stéphane Bancel, CEO, Moderna. Moderna’s COVID-19 vaccine was first tested in humans less than three months after news of the novel virus broke. But that lightning-fast development process belies the years of work that got Moderna to where it is today. The startup was founded in 2010 with the belief that mRNA technology, then still fairly new, could help treat any number of ailments. CEO Stéphane Bancel, pictured above, joined a year later. Moderna wasn’t originally focused on vaccines, but over time, its scientists began working toward vaccines against several infectious diseases as well as some forms of cancer. That experience came in handy when the COVID-19 pandemic arrived, leaving the world clamoring for a vaccine that could fight the deadly virus—and fast. Bancel’s company took the challenge in stride, using its mRNA platform to develop a vaccine around 95% effective at protecting against COVID-19 disease in less than a year. Cody O’Loughlin—The New York Times/Redux

When the COVID-19 pandemic hit a year ago, two innovative young pharmaceutical companies decided to try to harness this role played by messenger RNA: the German company BioNTech, which formed a partnership with the U.S. company Pfizer; and Moderna, based in Cambridge, Mass. Their mission was to engineer messenger RNA carrying the code letters to make part of the coronavirus spike protein—a string that begins CCUCGGCGGGCA … —and to deploy it in human cells.

BioNTech was founded in 2008 by the husband-and-wife team of Ugur Sahin and Ozlem Tureci, who met when they were training to be doctors in Germany in the early 1990s. Both were from Turkish immigrant families, and they shared a passion for medical research, so much so that they spent part of their wedding day working in the lab. They founded BioNTech with the goal of creating therapies that stimulate the immune system to fight cancerous cells. It also soon became a leader in devising medicines that use mRNA in vaccines against viruses.

In January 2020, Sahin read an article in the medical journal Lancet about a new coronavirus in China. After discussing it with his wife over breakfast, he sent an email to the other members of the BioNTech board saying that it was wrong to believe that this virus would come and go as easily as MERS and SARS. “This time it is different,” he told them.

BioNTech launched a crash project to devise a vaccine based on RNA sequences, which Sahin was able to write within days, that would cause human cells to make versions of the coronavirus’s spike protein. Once it looked promising, Sahin called Kathrin Jansen, the head of vaccine research and development at Pfizer. The two companies had been working together since 2018 to develop flu vaccines using mRNA technology, and he asked her whether Pfizer would want to enter a similar partnership for a COVID vaccine. “I was just about to call you and propose the same thing,” Jansen replied. The deal was signed in March.https://f0038f2a34d76ebd774c6dfa86a4f077.safeframe.googlesyndication.com/safeframe/1-0-38/html/container.html?n=0

By then, a similar mRNA vaccine was being developed by Moderna, a much smaller company with only 800 employees. Its chair and co-founder, Noubar Afeyan, a Beirut-born Armenian who immigrated to the U.S., had become fascinated by mRNA in 2010, when he heard a pitch from a group of Harvard and MIT researchers. Together they formed Moderna, which initially focused on using mRNA to try to develop personalized cancer treatments, but soon began experimenting with using the technique to make vaccines against viruses.

In January 2020, Afeyan took one of his daughters to a restaurant near his office in Cambridge to celebrate her birthday. In the middle of the meal, he got an urgent text message from the CEO of his company, Stéphane Bancel, in Switzerland. So he rushed outside in the freezing temperature, forgetting to grab his coat, to call him back.

Bancel said that he wanted to launch a project to use mRNA to attempt a vaccine against the new coronavirus. At that point, Moderna had more than 20 drugs in development but none had even reached the final stage of clinical trials. Nevertheless, Afeyan instantly authorized him to start work. “Don’t worry about the board,” he said. “Just get moving.” Lacking Pfizer’s resources, Moderna had to depend on funding from the U.S. government. Anthony Fauci, head of the National Institute of Allergy and Infectious Diseases, was supportive. “Go for it,” he declared. “Whatever it costs, don’t worry about it.”

It took Bancel and his Moderna team only two days to create the RNA sequences that would produce the spike protein, and 41 days later, it shipped the first box of vials to the National Institutes of Health to begin early trials. Afeyan keeps a picture of that box on his cell phone.

An mRNA vaccine has certain advantages over a DNA vaccine, which has to use a re-engineered virus or other delivery mechanism to make it through the membrane that protects the nucleus of a cell. The RNA does not need to get into the nucleus. It simply needs to be delivered into the more-accessible outer region of cells, the cytoplasm, which is where proteins are constructed.null

The Pfizer-BioNTech and Moderna vaccines do so by encapsulating the mRNA in tiny oily capsules, known as lipid nanoparticles. Moderna had been working for 10 years to improve its nanoparticles. This gave it one advantage over Pfizer-BioNTech: its particles were more stable and did not have to be stored at extremely low temperatures.

Katalin Kariko, Senior vice president, BioNTech. In 1995, after years of struggle, Hungarian-born Katalin Kariko was pushed off the path to full professorship at the University of Pennsylvania. Her work on mRNA, molecules she believed could fundamentally change the way humans treat disease, had stalled. Then, in 1997, she met and began working with immunologist Drew Weissman. In 2005, they published a study describing a modified form of artificial ­mRNA—a discovery, they argued, that opened the door to mRNA’s use in vaccines and other therapies. Eventually, Kariko and Weissman licensed their technology to the German company BioNTech, where Kariko, shown here in a portrait shot by a photographer working remotely, is now a senior vice president. Her patience paid off this year. The mRNA-based Pfizer-­BioNTech corona­virus vaccine, which Kariko helped develop, has been shown to be 95% effective at preventing COVID-19. Dina Litovsky—Redux for TIME

By November, the results of the Pfizer-BioNTech and Moderna late-stage trials came back with resounding findings: both vaccines were more than 90% effective. A few weeks later, with COVID-19 once again surging throughout much of the world, they received emergency authorization from the U.S. Food and Drug Administration and became the vanguard of the biotech effort to beat back the pandemic.

The ability to code messenger RNA to do our bidding will transform medicine. As with the COVID vaccines, we can instruct mRNA to cause our cells to make antigens—molecules that stimulate our immune system—that could protect us against many viruses, bacteria, or other pathogens that cause infectious disease. In addition, mRNA could in the future be used, as BioNTech and Moderna are pioneering, to fight cancer. Harnessing a process called immunotherapy, the mRNA can be coded to produce molecules that will cause the body’s immune system to identify and kill cancer cells.

RNA can also be engineered, as Jennifer Doudna and others discovered, to target genes for editing. Using the CRISPR system adapted from bacteria, RNA can guide scissors-like enzymes to specific sequences of DNA in order to eliminate or edit a gene. This technique has already been used in trials to cure sickle cell anemia. Now it is also being used in the war against COVID. Doudna and others have created RNA-guided enzymes that can directly detect SARS-CoV-2 and eventually could be used to destroy it.

More controversially, CRISPR could be used to create “designer babies” with inheritable genetic changes. In 2018, a young Chinese doctor used CRISPR to engineer twin girls so they did not have the receptor for the virus that causes AIDS. There was an immediate outburst of awe and then shock. The doctor was denounced, and there were calls for an international moratorium on inheritable gene edits. But in the wake of the pandemic, RNA-guided genetic editing to make our species less receptive to viruses may someday begin to seem more acceptable.https://f0038f2a34d76ebd774c6dfa86a4f077.safeframe.googlesyndication.com/safeframe/1-0-38/html/container.html?n=0

Throughout human history, we have been subjected to wave after wave of viral and bacterial plagues. One of the earliest known was the Babylon flu epidemic around 1200 B.C. The plague of Athens in 429 B.C. killed close to 100,000 people, the Antonine plague in the 2nd century killed 5 million, the plague of Justinian in the 6th century killed 50 million, and the Black Death of the 14th century took almost 200 million lives, close to half of Europe’s population.

The COVID-19 pandemic that killed more than 1.8 million people in 2020 will not be the final plague. However, thanks to the new RNA technology, our defenses against most future plagues are likely to be immensely faster and more effective. As new viruses come along, or as the current coronavirus mutates, researchers can quickly recode a vaccine’s mRNA to target the new threats. “It was a bad day for viruses,” Moderna’s chair Afeyan says about the Sunday when he got the first word of his company’s clinical trial results. “There was a sudden shift in the evolutionary balance between what human technology can do and what viruses can do. We may never have a pandemic again.”

The invention of easily reprogrammable RNA vaccines was a lightning-fast triumph of human ingenuity, but it was based on decades of curiosity-driven research into one of the most fundamental aspects of life on planet earth: how genes are transcribed into RNA that tell cells what proteins to assemble. Likewise, CRISPR gene-editing technology came from understanding the way that bacteria use snippets of RNA to guide enzymes to destroy viruses. Great inventions come from understanding basic science. Nature is beautiful that way.

Isaacson, a former editor of TIME, is the author of The Code Breaker: Jennifer Doudna, Gene Editing, and the Future of the Human Race, to be published in March. After the Pfizer vaccine was approved, he opted to remain in the clinical trial and has not yet been “unblinded.”

This appears in the January 18, 2021 issue of TIME.

More Must-Read Stories From TIME

---

• Moldovans Fear They’ll Be Putin’s Next Target. Their Prime Minister Is Preparing for the Worst
• This Is Why We’re Still Struggling With Anti-AAPI Hate One Year After Atlanta Shootings
• What to Know About a Fourth COVID-19 Vaccine Dose
• Evan Rachel Wood, Marilyn Manson and the Stories We Tell Ourselves About Iconoclastic Rock Stars
• After Fleeing Ukraine, LGBTQ Refugees Search for Safety in Countries Hostile to Their Rights
• A Haitian Man’s Brutal Experience With U.S. Border Agents Sparked Outrage. Now He’s Telling His Story
• ‘It’s Our Home Turf.’ The Man On Ukraine’s Digital Frontline

CONTACT US AT LETTERS@TIME.COM.

We Are God, Jesus, Holy Spirit, Force, The Trinity.

According to these scriptures whatever created us is telling us that we have dominion over the Earth we are supposed to be the ones protecting our beautiful planet and we are showing God or Nature whatever you like to refer to it as that we don’t give a darn.

Genesis 9:4-6

Only you shall not eat flesh with its life, that is, its blood. Surely I will require your lifeblood; from every beast I will require it. And from every man, from every man’s brother I will require the life of man. “Whoever sheds man’s blood,
By man his blood shall be shed,
For in the image of God
He made man.

Source: https://bible.knowing-jesus.com/topics/Blood,-As-Basis-Of-Life

New International Version.

Genesis 1:26
26 Then God said, “Let us(A) make mankind(B) in our image,(C) in our likeness,(D) so that they may rule(E) over the fish in the sea and the birds in the sky,(F) over the livestock and all the wild animals,[a] and over all the creatures that move along the ground.”

https://www.biblegateway.com/passage/?search=Genesis%201%3A26&version=NIV

Good News Translation.

Luke 17:21
No one will say, ‘Look, here it is!’ or, ‘There it is!’; because the Kingdom of God is within you.”

New International Version.

1 Corinthians 3:17
If anyone destroys God’s temple, God will destroy that person; for God’s temple is sacred, and you together are that temple.

New Living Translation.

Hebrews 10:24
Let us think of ways to motivate one another to acts of love and Good works.

Berean Study Bible.

Hebrews 10:25
Let us not neglect meeting together, as some have made a habit, but let us encourage one another, and all the more as you see the Day approaching.

We are God or Good.

Isn’t Star Wars about the Force that is everything and that is in everything?
https://vm.tiktok.com/ZTdPVHxPG/

Evidence for a connection between Disease-19 and exposure to radiofrequency radiation from wireless communications including 5.G.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580522/

Natural immunity was more effective than 💉 alone against delta variant, CDC study shows.
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The 1986 Act
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https://t.me/Covid19VaccinationsSideEffects

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This website will be where you can find more information. Just give us some time to update it please.
https://LiveTruthDaily.WordPress.com

The Purity Virus (The X-Files Explored)
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Super Portable Walking-Stick Wood Stoves.
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The BEST NEWS re CΟRΟNΑ VΙrus you’ve heard all month! Kinda.
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Area 51 2005 Game Diary Clip.🧬💉🧫
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Stop Scrolling Black Lights….
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5G Zombies movie on Tubi app.
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What did Mark Zuckerberg say about the 💉?
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5G NEW WORLD ORDER MIND CONTROL GRID LINKS TARGETED INDIVIDUALS TO A.I. QUANTUM SUPERCOMPUTER.
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What is in the 💉?
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Bill Gates 2005 briefing the Government on removing the God Gene 🧬💉🧫
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Sickness from 5G Cell Towers | Technology is Killing Us Slowly.
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Bill Gates: How Gene Editing, AI Can Benefit World’s Poorest.
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#WeAreGod, #Jesus, Holy Spirit, #Force, The #Trinity.

Genetically modified organism.

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“GMO” redirects here. For other uses, see GMO (disambiguation).
A genetically modified organism (GMO) is any organism whose genetic material has been altered using genetic engineering techniques. The exact definition of a genetically modified organism and what constitutes genetic engineering varies, with the most common being an organism altered in a way that “does not occur naturally by mating and/or natural recombination”. A wide variety of organisms have been genetically modified (GM), from animals to plants and microorganisms. Genes have been transferred within the same species, across species (creating transgenic organisms), and even across kingdoms. New genes can be introduced, or endogenous genes can be enhanced, altered, or knocked out.

Creating a genetically modified organism is a multi-step process. Genetic engineers must isolate the gene they wish to insert into the host organism and combine it with other genetic elements, including a promoter and terminator region and often a selectable marker. A number of techniques are available for inserting the isolated gene into the host genome. Recent advancements using genome editing techniques, notably CRISPR, have made the production of GMOs much simpler. Herbert Boyer and Stanley Cohen made the first genetically modified organism in 1973, a bacterium resistant to the antibiotic kanamycin. The first genetically modified animal, a mouse, was created in 1974 by Rudolf Jaenisch, and the first plant was produced in 1983. In 1994, the Flavr Savr tomato was released, the first commercialized genetically modified food. The first genetically modified animal to be commercialized was the GloFish (2003) and the first genetically modified animal to be approved for food use was the AquAdvantage salmon in 2015.

Bacteria are the easiest organisms to engineer and have been used for research, food production, industrial protein purification (including drugs), agriculture, and art. There is potential to use them for environmental purposes or as medicine. Fungi have been engineered with much the same goals. Viruses play an important role as vectors for inserting genetic information into other organisms. This use is especially relevant to human gene therapy. There are proposals to remove the virulent genes from viruses to create vaccines. Plants have been engineered for scientific research, to create new colors in plants, deliver vaccines, and to create enhanced crops. Genetically modified crops are publicly the most controversial GMOs, in spite of having the most human health and environmental benefits.[1] The majority are engineered for herbicide tolerance or insect resistance. Golden rice has been engineered with three genes that increase its nutritional value. Other prospects for GM crops are as bioreactors for the production of biopharmaceuticals, biofuels, or medicines.

Animals are generally much harder to transform and the vast majority are still at the research stage. Mammals are the best model organisms for humans, making ones genetically engineered to resemble serious human diseases important to the discovery and development of treatments. Human proteins expressed in mammals are more likely to be similar to their natural counterparts than those expressed in plants or microorganisms. Livestock is modified with the intention of improving economically important traits such as growth rate, quality of meat, milk composition, disease resistance, and survival. Genetically modified fish are used for scientific research, as pets, and as a food source. Genetic engineering has been proposed as a way to control mosquitos, a vector for many deadly diseases. Although human gene therapy is still relatively new, it has been used to treat genetic disorders such as severe combined immunodeficiency and Leber’s congenital amaurosis.

Many objections have been raised over the development of GMOs, particularly their commercialization. Many of these involve GM crops and whether food produced from them is safe and what impact growing them will have on the environment. Other concerns are the objectivity and rigor of regulatory authorities, contamination of non-genetically modified food, control of the food supply, patenting of life, and the use of intellectual property rights. Although there is a scientific consensus that currently available food derived from GM crops poses no greater risk to human health than conventional food, GM food safety is a leading issue with critics. Gene flow, impact on non-target organisms, and escape are the major environmental concerns. Countries have adopted regulatory measures to deal with these concerns. There are differences in the regulation for the release of GMOs between countries, with some of the most marked differences occurring between the US and Europe. Key issues concerning regulators include whether GM food should be labeled and the status of gene-edited organisms.

Evidence for a connection between Disease-19 and exposure to radiofrequency radiation from wireless communications including 5.G.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580522/

Natural immunity was more effective than 💉 alone against delta variant, CDC study shows.
https://www.google.com/amp/s/fox8.com/news/coronavirus/natural-immunity-was-more-effective-than-vaccines-alone-against-delta-variant-cdc-study-shows/amp/

Are There Dangers To Wearing Masks?
https://t.me/AreThereDangersToWearingMasks

The 1986 Act
https://www.congress.gov/bill/99th-congress/house-bill/5546

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https://t.me/Covid19VaccinationsSideEffects

Live Truth Daily Social
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This website will be where you can find more information. Just give us some time to update it please.
https://LiveTruthDaily.WordPress.com

The BEST NEWS re CΟRΟNΑ VΙrus you’ve heard all month! Kinda.
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5G Zombies movie on Tubi app.
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In Bosnia in 2005, an amateur archeologist named Semir Osmanagich announced that he had discovered a pyramidal complex at the foot of a the hill now known as the Pyramid of the Sun which is some 1,180 feet high. Over time, he discovered three more pyramids and proposed that they were built by the same people who created the pyramids of Egypt and Mesoamerica. Osmanagich has claimed the pyramids to be 34,000 years old.

Not only were they found to be more precise in orientation than the pyramids of Giza but blocks made of some type of concrete were found at the Sun pyramid’s base. Futhermore, physicists surprisingly measured an electromagnetic energy of 28khz emanating from the tip of the pyramid.
.
In 2008, a conference of 50 scientists from countries including Egypt, Russia, UK, Poland, was conducted. The experts supported the claim that the hills were actually pyramids. Subsequent annual conferences concluded that the Bosnian pyramid complex is the oldest in the world.

Evidence for a connection between Disease-19 and exposure to radiofrequency radiation from wireless communications including 5.G.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580522/

Natural immunity was more effective than 💉 alone against delta variant, CDC study shows.
https://www.google.com/amp/s/fox8.com/news/coronavirus/natural-immunity-was-more-effective-than-vaccines-alone-against-delta-variant-cdc-study-shows/amp/

Are There Dangers To Wearing Masks?
https://t.me/AreThereDangersToWearingMasks

The 1986 Act
https://www.congress.gov/bill/99th-congress/house-bill/5546

C.o.v.id-19 V.a.c.c.i.n.a.t.i.o.n.s Side Effects
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This website will be where you can find more information. Just give us some time to update it please.
https://LiveTruthDaily.WordPress.com

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https://www.bitchute.com/video/V6G7XUV4PGiB/

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1,000 friends, but not one of them helped her Mother’s anger as woman posts suicide note on Facebook before killing herself!!!!

INDEPENDENT Contribute Subscribe

Jerome Taylor• Thursday 06 January 2011 01:00

The mother of a middle-aged woman who announced her intention to commit suicide to more than 1,000 of her Facebook friends has angrily demanded why not a single one of them came to her aid before she died.

Simone Back, 42, from Brighton, took an overdose of pills on Christmas Day and posted a brief suicide note that evening on the social networking site expressing her intention to die. Friends who lived outside the city urged others in Brighton to check on her, but the calls went unread or unheeded. Police found her the next day and she was pronounced dead in hospital.

Her 60-year-old mother, Jennifer Langridge, was only alerted to the Facebook message on Boxing Day afternoon, 17 hours after her daughter’s original posting. She dialled 999 but when police broke into the flat, Ms Back was already unconscious. “Nobody told me anything about it until the following day when I was sent a text saying: ‘get help’,” Ms Langridge said. “It is upsetting to think nobody did anything for my daughter.” Ms Langridge, who is disabled and has limited mobility, said she believed more could have been done to help her daughter.

“Normal help for her,” Ms Langridge said. “I watched my daughter go from a lovely when she takes overdoses I get young woman to what she ended up as: someone who didn’t smile.”

Friends also expressed anger that Ms Back’s threat to kill herself was not taken more seriously. Samantha Pia Owen, 48, from Southampton, said: “Somebody could have helped. They were all posting how much they care for her but someone should have at least popped round to see that she was OK.

“Everyone just carried on arguing with each other on Facebook like it wasn’t happening. Some of those people lived within walking distance of Simone. If one person just left their computer and went to her house her life could have been saved.”

Postings on Ms Back’s Facebook page reveal that many of her friends did not take her suicide threats seriously because she had threatened to kill herself on previous occasions. At 10.53pm on Christmas Day, Ms Back posted the suicide note, part of which read: “Took all my pills be dead soon so bye bye every one.”

A series of messages were then left on the same thread, with some of her friends expressing concern about whether Ms Back had gone through with her threat. One wrote: “did ya’ll catch the part about simone taking a shytload of pills??.. the ‘bye bye’ part?? Did anyone go by personally and check on simone… or call 9/11?? What’s wrong with you people??”

Another friend replied: “She does it all the time, takes all of her pills.” Others urged people to go round to Ms Back’s flat. “If any of you lot actually call youself a friend one of you should call around and see if shes ok, so glad I don’t personally know any of you, heartless,” wrote one.

Initial reports from friends suggested that Ms Back had been the victim of cyber- bullying, but later posts from friends say she had recently split up with her girlfriend.

Her Facebook page was filled with tributes and messages of support yesterday. One read: “Dearest Simone… May you have found peace at last. You will be greatly missed but your legacy will go on.”

A spokeswoman from the mental health charity Mind said suicide threats should be taken seriously: “It is a myth that people who talk about suicide don’t go through with it. They are very likely to have spoken about their feelings of desperation to others. ” %3D

A spokesperson from Facebook said: “We were deeply saddened to hear of the recent suicide of Simone Back. We have a close working relationship with the Samaritans and have a process in place whereby friends and family who are concerned about someone can report it to us through the Help Centre.

“A team of trained professionals are then able to review the case and the Samaritans will make contact with the person at risk. The safety of people who use Facebook is of paramount importance to us and this system is just one of number of tools we have in place to help them stay safe.”

This website will be where you can find more information. Just give us some time to update it please.
https://LiveTruthDaily.WordPress.com

https://www-independent-co-uk.cdn.ampproject.org/v/s/www.independent.co.uk/life-style/gadgets-and-tech/news/1-000-friends-but-not-one-of-them-helped-her-2177037.html?amp_js_v=a6&amp_gsa=1&amp&usqp=mq331AQKKAFQArABIIACAw%3D%3D#aoh=16467090495765&referrer=https%3A%2F%2Fwww.google.com&amp_tf=From%20%251%24s&ampshare=https%3A%2F%2Fwww.independent.co.uk%2Ftech%2F1-000-friends-but-not-one-of-them-helped-her-2177037.html

There are many horrific injection side effects like this poor lady is saying!
………………..
Just because something is stated doesn’t make it true or false. If you want to know the truth keep searching with balance in life. Matthew 7:7
………………………………………………………………………………
Evidence for a connection between Disease-19 and exposure to radiofrequency radiation from wireless communications including 5.G.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580522/

Natural immunity was more effective than  alone against delta variant, CDC study shows.
https://www.google.com/amp/s/fox8.com/news/coronavirus/natural-immunity-was-more-effective-than-vaccines-alone-against-delta-variant-cdc-study-shows/amp/

Are There Dangers To Wearing Masks?
https://t.me/AreThereDangersToWearingMasks

The 1986 Act
https://www.congress.gov/bill/99th-congress/house-bill/5546

C o v id-19 V a c c i n a t i o n s Side Effects
https://t.me/Covid19VaccinationsSideEffects

Live Truth Daily Social
https://t.me/LiveTruthDailySocial

This website will be where you can find more information. Just give us some time to update it please.
https://LiveTruthDaily.WordPress.com

YouTube Censors Viral Video Of California Doctors Exposing The Governments So-Called Science.
https://www.bitchute.com/video/YXvjoGGClrhM/

Super Portable Walking-Stick Wood Stoves.
https://www.bitchute.com/video/ml0RflMos5Ns/

The BEST NEWS re C Ο R Ο N Α V Ι r us you’ve heard all month! Kinda.
https://www.bitchute.com/video/3MhGJw8cuVyP/

Area 51 2005 Game Diary Clip.溺匿
https://www.bitchute.com/video/SvW6pqcdegSs/

Stop Scrolling Black Lights….
https://www.bitchute.com/video/V6G7XUV4PGiB/

5G Zombies movie on Tubi app.
https://www.bitchute.com/video/1CggUwAlAM9D/

What did Mark Zuckerberg say about the ?
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5G NEW WORLD ORDER MIND CONTROL GRID LINKS TARGETED INDIVIDUALS TO A.I. QUANTUM SUPERCOMPUTER.
https://www.bitchute.com/video/9EDgS4XJcj3q/

What is in the ?
https://www.bitchute.com/video/6rMrIcG3ThRQ/

Bill Gates 2005 briefing the Government on removing the God Gene 溺匿
https://www.bitchute.com/video/QggfIrliLQDF/

Sickness from 5G Cell Towers | Technology is Killing Us Slowly.
https://www.bitchute.com/video/JrAs3a3YhrFE/

Bill Gates: How Gene Editing, AI Can Benefit World’s Poorest.
https://www.bitchute.com/video/mxUkwW7uIy5A/

Between 1534 and 1542, Jacques Cartier made three voyages across the Atlantic, claiming the land for King Francis I of France. Cartier heard two captured guides speak the Iroquoian word kanata, meaning “village.” By the 1550s, the name of Canada began appearing on maps.Oct 26, 2015
Combatants: British Empire; Allies of World War II

https://www.canada.ca/en/immigration-refugees-citizenship/corporate/publications-manuals/discover-canada/read-online/canadas-history.html#:~:text=Between%201534%20and%201542%2C%20Jacques,Canada%20began%20appearing%20on%20maps.
………………..
Just because something is stated doesn’t make it true or false. If you want to know the truth keep searching with balance in life. Matthew 7:7
………………………………………………………………………………
Evidence for a connection between Disease-19 and exposure to radiofrequency radiation from wireless communications including 5.G.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580522/

Natural immunity was more effective than 💉 alone against delta variant, CDC study shows.
https://www.google.com/amp/s/fox8.com/news/coronavirus/natural-immunity-was-more-effective-than-vaccines-alone-against-delta-variant-cdc-study-shows/amp/

Are There Dangers To Wearing Masks?
https://t.me/AreThereDangersToWearingMasks

The 1986 Act
https://www.congress.gov/bill/99th-congress/house-bill/5546

C o v id-19 V a c c i n a t i o n s Side Effects
https://t.me/Covid19VaccinationsSideEffects

Live Truth Daily Social
https://t.me/LiveTruthDailySocial

This website will be where you can find more information. Just give us some time to update it please.
https://LiveTruthDaily.WordPress.com

YouTube Censors Viral Video Of California Doctors Exposing The Governments So-Called Science.
https://www.bitchute.com/video/YXvjoGGClrhM/

Super Portable Walking-Stick Wood Stoves.
https://www.bitchute.com/video/ml0RflMos5Ns/

The BEST NEWS re C Ο R Ο N Α V Ι r us you’ve heard all month! Kinda.
https://www.bitchute.com/video/3MhGJw8cuVyP/

Area 51 2005 Game Diary Clip.🧬💉🧫
https://www.bitchute.com/video/SvW6pqcdegSs/

Stop Scrolling Black Lights….
https://www.bitchute.com/video/V6G7XUV4PGiB/

5G Zombies movie on Tubi app.
https://www.bitchute.com/video/1CggUwAlAM9D/

What did Mark Zuckerberg say about the 💉?
https://www.bitchute.com/video/RtTRTmnraLOT/

5G NEW WORLD ORDER MIND CONTROL GRID LINKS TARGETED INDIVIDUALS TO A.I. QUANTUM SUPERCOMPUTER.
https://www.bitchute.com/video/9EDgS4XJcj3q/

What is in the 💉?
https://www.bitchute.com/video/6rMrIcG3ThRQ/

Bill Gates 2005 briefing the Government on removing the God Gene 🧬💉🧫
https://www.bitchute.com/video/QggfIrliLQDF/

Sickness from 5G Cell Towers | Technology is Killing Us Slowly.
https://www.bitchute.com/video/JrAs3a3YhrFE/

Bill Gates: How Gene Editing, AI Can Benefit World’s Poorest.
https://www.bitchute.com/video/mxUkwW7uIy5A/

Used between the 1500s and 1800s, the ‘scold’s Bridle’ was a device which was used to publicly humiliate women who were forced to wear it. On the inside, the device had a metal plate that would go inside the mouth and press down on the tongue to stop the wearer from speaking. It would be placed on women who were deemed to be ‘troublesome’ to keep them quiet and ‘stop them from gossiping.’

This is so messed up! Has anyone ever watched “The Haunting on House Hill” on Netflix and if so is it worth watching??

The BEST NEWS re C Ο R Ο N Α VΙrus you’ve heard all month! Kinda.
https://www.bitchute.com/video/3MhGJw8cuVyP/

This website will be where you can find more information. Just give us some time to update it please.
https://LiveTruthDaily.WordPress.com