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How the Government Uses Fear to Control


Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2020/09/19/government-using-fear-to-control.aspx
Analysis by Dr. Joseph Mercola    Fact Checked    September 19, 2020

STORY AT-A-GLANCE

  • August 28, 2020, the Children’s Health Defense, led by Robert F. Kennedy Jr., launched a European branch of the organization
  • Totalitarian nations have always used the power of fear to make citizens comply with authoritarian rule. Without fail, it’s been shown that all you have to do to engineer compliance, no matter how horrific the ramifications, is to tell people they have something to fear, and claim they will be safe if they follow you
  • Today, we also have something no previous tyrant has had, namely the technology to track, trace, control and manipulate individuals wherever they live. Most are surrounded by electronics and wireless devices that harvest every imaginable data point about their personal life
  • Digital currency will complete the net of tyranny. Once all cash economies have been abolished, they have absolute control over us because they will be able to tax every transaction and ensure compliance through the threat of financial confiscation
  • The pushback seen around the world against mask mandates, vaccines, social distancing and lockdowns is not because there’s a willful ignorance of science, but that no real science is being presented; science is actually being withheld and suppressed

August 28, 2020, the Children’s Health Defense, led by Robert F. Kennedy Jr., launched a European branch of the organization. In a press conference1 announcing the new branch, Kennedy discussed how governments are using fear to control and manipulate the population.

Acting as quasi-government agencies, public health organizations such as the U.S. Centers for Disease Control and Prevention and the World Health Organization are pushing vaccines using the same fear tactics, while simultaneously removing the regulatory oversight that used to ensure vaccines are properly safety-tested.

Corruption in the political system, however, has destroyed the trust these agencies need to get people to willingly take these fast-tracked vaccines, and this despite the fact that the media keep regurgitating the prescribed propaganda. Kennedy also highlights how people like Dr. Anthony Fauci and Bill Gates are helping to promote this global vaccination agenda.

“Point a finger at that source of their fear and you can make human beings do anything you want. You can make them go to the slaughter like sheep; you can make them obey.” ~ Robert F. Kennedy Jr.

As a result of all this corruption, there’s no independent, unbiased buffer between greedy corporations and the world’s most vulnerable populations — our children. This is a global problem, Kennedy says, and the press is facilitating it by helping to create so much fear in the peoples’ minds that they will obey whatever the health agencies say, no matter how illogical the demands.

Vaccines Are Not Routinely Tested Against Placebo

Kennedy explains how he ended up spearheading the fight for vaccine safety. He runs the largest water protection group in the world, the Waterkeeper Alliance. In the early 2000s, he was involved in lawsuits over mercury discharges by coal burning power plants.

Around the same time, he learned of the presence of mercury in vaccines, and that this source was a much larger source of mercury exposure than contaminated fish was. Initially, his goal was simply to get the mercury removed from vaccines, but as he dug deeper, he realized “there were larger problems with vaccines.”

One of the biggest problems was, and still is, the fact that vaccines in the U.S. are not safety tested. “They have an exemption that is not available to any other medical product,” Kennedy says, explaining that when the vaccine program was initially launched, the goal was to make sure vaccines could be rapidly developed and deployed in response to biological attacks by foreign countries.

As a result, regulatory impediments — including safety testing vaccines against placebos, which the gold-standard in medical safety testing — were removed.

My very narrow purpose in starting the Children Health Defense was to address this problem and to get vaccines properly safety tested, because if they’re not safety tested, nobody can tell you with any medical authority whether that vaccine is injuring more people than it’s saving,” Kennedy says.2

“As we continued on with this advocacy it became very clear that there were other problems as well. There [were] problems with the corruption in our political system.

The pharmaceutical companies had not only corrupted our politicians with huge amounts of lobbying money, they had captured the agencies that are supposed to protect Americans from public health threats: the CDC, the FDA, the HHS. They had captured the press in our country by huge influxes of advertising dollars which had neutralized the press.

They had effectively subverted American democracy by neutralizing all of those institutions that the Founding Fathers of our nation had created to stand between a greedy corporation and a vulnerable child.

The Congress had been corrupted. The regulatory agencies were captured; they had become the sock puppets for the industry they’re supposed to regulate. The press had been sidelined.

And worst of all, they had passed a law in our country in 1986 that gave pharmaceutical companies complete immunity from liability. So, there was no incentive for any of those companies to make vaccines safe …

If we win this battle in just one nation, the United States, we’re still going to lose it globally. So, we need people of good will, people who have courage, people who have a nonconformist way of thinking, who understand that we are being lied to, that the entire political structure today is saturated in pharmaceutical propaganda.”

Click here to read more

The Power of Fear

As noted by Kennedy, totalitarian nations have always used the power of fear to make citizens comply with authoritarian rule. Without fail, it’s been shown that all you have to do to engineer compliance, no matter how horrific the ramifications, is to tell people they have something to fear, and that they will be safe if they follow your lead.

“Point a finger at that source of their fear and you can make human beings do anything you want. You can make them go to the slaughter like sheep; you can make them obey,” Kennedy says.

A famous quote by Franklin D. Roosevelt is “The only thing we have to fear is fear itself.” He understood that fear is ultimately what strips us of our human rights and drives a society into totalitarianism, and that the only way to circumvent such a fate is to bravely resist fear. Today, one of the biggest threats (or so we’re told) is global pandemics.

“Governments love pandemics the same way that they love wars because it gives them power; it gives them control and it gives them the capacity to impose obedience on human beings,” Kennedy notes.

Today, we also have something no previous tyrant has had, namely the technology to track, trace, control and manipulate individuals wherever they live. Most people are surrounded by electronics and wireless devices that harvest every imaginable data point about your personal life.

Digital currency will complete the net of tyranny. Once all cash economies have been abolished, “they have absolute control over us because they will be able to tax every transaction,” Kennedy says. A digital currency economy will also ensure total compliance by the masses. If you disobey, they can simply restrict or shut down your bank account.

“Many people argue that this pandemic was a plandemic, that it was planned from the outset, it’s part of a sinister scheme,” Kennedy says. “I can’t tell you the answer to that. I don’t have enough evidence.

A lot of it feels very planned to me. I don’t know, but I will tell you this, if you create these mechanisms for control, they become weapons of obedience for authoritarian regimes no matter how beneficial or innocent the people who created them. Once you create them, they will be abused; 100% guarantee that they will be abused.”

People in Authority Lie

Kennedy goes on to stress that the pushback seen around the world against mask mandates, vaccines, social distancing and lockdowns are not because there’s a willful ignorance of science, but that no real science is being presented; science is actually being withheld and suppressed.

“What we know is that we’re not being dealt with honestly,” he says. “We’re being told, ‘This is the science,’ but it’s an appeal to authority. It’s science because Tony Fauci and Bill Gates tell us it’s science.

We want to see the studies. We want to see the studies on hydroxychloroquine. We want to see the studies on whether the lockdown is killing more people than the coronavirus. We want to see real science and real risk assessment.

My father told me when I was a child, ‘People in authority lie.’ If we are going to continue to live in a democracy we need to understand that people in authority lie. People in authority will abuse every power that we relinquish to them, and right now we are giving them the power to micromanage every bit of our lives.

Twenty-four hours a day they’re going to know where we are, they’re going to know the money that we spend, they’re going to have access to our children. They’re going to have the right to compel unwanted medical interventions on us.”

Why Are We Ignoring the Nuremberg Charter?

As noted by Kennedy, this is precisely what the Nazis did to prisoners during World War II. After the war, the world was so horrified by the atrocities of the Nazi camps, including and especially the medical testing that took place, the Nuremberg Code,3 which details the ethical framework for medical experimentation, was enacted.

“We all pledged … we would never again impose unwanted medical interventions on human beings without informed consent,” Kennedy says. “Yet in two years, all of that conviction has suddenly disappeared. People are walking around in masks when the science has not been explained to them. They are doing what they’re told.

These government agencies are orchestrating obedience, and it is not democratic; it’s not the product of democracy. It’s the product of a pharmaceutical driven, biosecurity agenda that will enslave the entire human race and plunge us into a dystopian nightmare where the apocalyptical forces of ignorance and greed will be running our lives and ruining our children … 

The launch of this organization, Children’s Health Defense, in Europe is a beachhead; it’s an announcement to the world that we are not going to take it. We are building institutions to fight your institutions. You have global institutions and we now have a global institution …

We are not going to let you take our democracy away. We are not going to let you take our health away. We are not going to let you take our freedoms away. We are not going to let you take our children away.”

Do Not Trust the Medical or National Security Establishment

In the Ron Paul Liberty Report above, former Congressman Dr. Ron Paul interviews4 Kennedy about who really killed his father and uncle, and why. In summary, the evidence suggests his father, Robert Kennedy, was assassinated by a CIA agent hired as a security guard.

Kennedy reviews some of the history of the CIA — how it was initially established as an espionage organization tasked solely with intelligence gathering, only to transform into a paramilitary agency engaged with the overthrowing of democracies around the world and other nefarious and antidemocratic activities.

He also touches on the infamous CIA program called MK Ultra, in which individuals are brainwashed to carry out orders, including murders, against their own will.

The conversation eventually turns to vaccine safety and the folly of ignoring published science showing there are significant problems — problems that the medical establishment is refuting without any actual counter-evidence.

They also discuss data suggesting the COVID-19 lockdowns may have caused more deaths than the virus itself, as well as the civil rights issues involved. “I think the data are really clear, that quarantine is going to kill far more people than COVID-19” Kennedy says.

Pandemic Responses Are Doing Far More Harm Than Good

He cites research from the 1980s that looked at the impact of unemployment on human life. This kind of research flourished in the wake of American industries increasingly being shipped overseas, causing rising unemployment.

The most famous of these studies, Kennedy says, found that for every one-point rise in unemployment there were 37,000 excess deaths, 4,000 excess imprisonments and 3,300 excess admissions into mental institutions.

“In addition to that, we have disruptions to medical supply chains and food supply,” Kennedy notes. “There are millions of people starving around the world because of the quarantines. We’ve lost, already, about 50,000 minority businesses, permanently, in [the U.S.] What is that going to do?”

Kennedy cites a report from a hospital in San Francisco that stated they saw one year’s-worth of suicides in a single month, a 1,200% increase. He also cites British research showing that while there were 30,000 excess deaths in nursing homes during a five-week period during the lockdown, only one-third of them were due to COVID-19.

In other words, the death rate from isolation was double that of the virus itself. People didn’t get the proper medical care for chronic conditions and so on. Kennedy also rightly points out that what we will see — and are already seeing — is the obliteration of the middle-class and the shift of wealth from the poor to the already ultra-rich.

Then there’s the rapidly approaching question of vaccination. Children and young adults under the age of 20 basically have a zero risk of dying from COVID-19, so are we going to force them to gamble with their future health by taking a fast-tracked and unproven vaccine in the name of protecting the elderly who are at greatest risk of dying from COVID-19? “That is a very dicey ethical question,” Kennedy says.

“This is like an apocalyptical battle; it’s really something I never thought would happen in my lifetime, where all the values of our country are being eroded,” Kennedy says, pointing out that in 1968, there was a bird flu pandemic5 that had a higher mortality rate than COVID-19, “and we all went to Woodstock. It was just part of life.”

Today, pandemics have become a tool of tyranny, and the “biosecurity” agenda is a globalist agenda that ultimately seeks to gain total control by stripping away human rights and the rights of countries. As noted by Kennedy, the fear level is totally out of proportion to the real threat of COVID-19, as are the government-prescribed responses.

Season 2, Episode 2 of “TRUTH” with Robert F. Kennedy, Jr.

© 18th September 2020 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc.
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Your donation will help to support us in our efforts.
Reproduced from original article:
childrenshealthdefense.org/news/season-2-episode-2-of-truth-with-robert-f-kennedy-jr
SEPTEMBER 18, 2020

In the second episode of our second season of “TRUTH” with Robert F. Kennedy, Jr., Mr. Kennedy interviewed life coach and internet comedian J. P. Sears.  The two had a lively and thought-provoking conversation that centered on several themes relevant to the COVID crisis including:

  • How censorship leads to totalitarianism and the importance of the First Amendment
  • Children’s Health Defense’s lawsuit against Facebook
  • Keeping a healthy attitude in troubling times
  • The toll on human life from deaths of despair vs. the coronavirus
  • The physical and societal impacts of mask mandates
  • The consequences of living in fear

(All episodes can be found on CHD’s social media, and on the CHD Channel found on Peeps TV, a network on Roku. Roku is accessible from any Smart TV and can be purchased separately for older TVs.)

Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is planning many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.

AstraZeneca’s COVID-19 vaccine trial ON HOLD after participant had serious neurological symptom

Reproduced from original article:
www.naturalhealth365.com/covid-trial-on-hold-3556.html
by:  | September 15, 2020

astrazeneca-covid-trial(NaturalHealth365) While vaccines generally take 15-20 years to get to the market, there’s been a significant push to get a COVID-19 vaccine ready to use to combat the current global pandemic. In fact, we previously reported that vaccines are being rushed to market while skipping procedures like animal testing before being used on humans.

We already know that most vaccine candidates fail, so testing them on humans without proper safety precautions could result in a solution that’s worse than the virus. Backing up our concerns is recent news announcing that AstraZeneca’s Phase 3 COVID-19 trials were put on hold after a participant in the United Kingdom experienced serious neurological symptoms.

Patient developed symptoms consistent with transverse myelitis after COVID-19 vaccine

According to reports by Stat News, a woman who was a part of the Phase 3 COVID-19 AstraZeneca vaccine trials came down with neurological symptoms that were consistent with transverse myelitis, a very serious and rare spinal inflammatory disorder.  AstraZeneca did confirm that this woman had been injected with the vaccine and not a placebo in the trials.  In addition, this participant was diagnosed with multiple sclerosis upon further examination, although this diagnosis was deemed to be unrelated to being treated with the COVID-19 vaccine.

While sources say the woman is expected to recover from her symptoms, the symptoms were enough to put the Phase 3 trials on hold – at least within the U.K.  It remains unclear whether the pause on Phase 3 testing within the U.K. will affect plans for Phase 3 testing within the United States.

Along with this isolated report of serious neurological symptoms, studies on phase one and two, which were published in the medical journal the Lancet discovered multiple side effects. These side effects include reactions at the injection site, headaches, muscle pain, and fever, although they did subside during the course of the vaccine trials.

Adenovirus used in AstraZeneca’s COVID-19 vaccine

The AstraZeneca vaccine, which is called AZD1222, uses an adenovirus carrying a gene for one of the proteins found in SARS-CoV-2, which is the virus causing COVID-19.  Scientists believe the adenovirus will cause the immune system to generate a protective response to SARS-2. While this platform hasn’t been used in any vaccines that have gained approval, it’s been tested in experimental vaccines designed for other viruses, such as the Ebola virus.

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The advenovirus platform is still considered “experimental,” although it did serve as the basis for a COVID-19 vaccine in Russia. Known as Sputnik-V, this new vaccine was rolled out to the public in Russia within the past week.

According to a peer-reviewed study, which was published in the Lancet, that looked at early testing of the Sputnik-V vaccine, the Russian vaccine appears to be safe and effective.  Naturally, we have our doubts.

It should be noted that most of these vaccine “trials,” involve relatively “young, healthy people.”  One can only imagine what the results of these experimental COVID-19 vaccine trials would be, if they were done with an elderly population.  And, that’s not to mention testing this new vaccine on people with diabetes, obesity or on multiple prescription medications for preexisting health issues.

So, obviously, the jury is still out on what will happen with AstraZeneca’s vaccine moving forward.  Feeding into the general public distrust about vaccines, many other vaccine manufacturers remain quite secretive about their “progress.”

Editor’s note: Just a few days after the AstraZeneca trial was suspended – due to a spinal inflammatory response in one participant, the company announced it will resume its work on developing a vaccine.  But, AstraZeneca is not disclosing any medical information.  Naturally, this leaves many people concerned about what’s really going on here.

Stay tuned to NaturalHealth365, as we continue to monitor developments in this story.

Sources for this article include:

StatNews.com
RT.com
TheLancet.com
NaturalHealth365.com

EcoHealth Alliance Gets Big Bucks for Risky Virus Research


Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2020/09/17/gain-of-function-research.aspx
Analysis by Alexis Baden-Mayer    September 17, 2020

gain of function research

STORY AT-A-GLANCE

  • Gain-of-function research to alter coronaviruses for the infection of humans goes back to 1999 or earlier, years before the first novel coronavirus outbreak
  • Peter Daszak, President of EcoHealth Alliance, is a top scientific collaborator, grant writer and spokesperson for virus hunters and gain-of-function/dual-use researchers, in labs both military and civilian
  • On behalf of the U.S. government, often the military, Daszak scours the globe for animal pathogens and brings them back to the lab to be catalogued, investigated and manipulated
  • To learn that the closest known relative to SARS-CoV-2 has been in the care of the gain-of-function researchers at the Wuhan Institute of Virology (WIV) for seven years does nothing to allay suspicions that the virus infected humans only after being tinkered with in a lab
  • The National Institute of Allergy and Infectious Diseases announced a five-year, $82-million investment in a new global network of Centers for Research in Emerging Infectious Diseases, including gain-of-function experiments to “determine what genetic or other changes make [animal] pathogens capable of infecting humans”

Peter Daszak, President of EcoHealth Alliance, is a top scientific collaborator, grant writer and spokesperson for virus hunters and gain-of-function/dual-use researchers, in labs both military and civilian.

Daszak works with dozens of high-containment laboratories around the world that collect pathogens and use genetic engineering and synthetic biology to make them more infectious, contagious, lethal or drug-resistant. These include labs controlled by the U.S. Department of Defense, in countries in the former Soviet Union, the Middle East, South East Asia and Africa.

Many of these labs are staffed by former biological weapons scientists. (See Arms Watch’s reports.1) Before the Biological Weapons Convention was ratified, this research was called what it is: biological weapons research. Now, it’s euphemistically called gain-of-function or dual-use research.

Gain-of-function research to alter coronaviruses for the infection of humans2 goes back to 1999 or earlier,3 years before the first novel coronavirus outbreak. On behalf of the U.S. government, often the military, Daszak scours the globe for animal pathogens and brings them back to the lab to be catalogued, investigated and manipulated.

Daszak and others justify their research this way: If/When an outbreak of a new virus occurs, they can compare it to the ones in their labs, and maybe glean how the novel virus emerged. A recent Wired magazine article4 quoting Daszak described how a virus collected in 2012 was found to be a 96% match to SARS-CoV-2 in 2020:

“The search for the source of SARS – which killed more than 770 people two decades ago – has given us a headstart for the current hunt.

Wearing hazmat suits and equipped with mist nets, a team from the Wuhan Institute of Virology, together with the ecologist and president of EcoHealth Alliance Peter Daszak, ventured into limestone caves to collect faeces and blood samples from thousands of roosting bats before testing them for novel coronaviruses in the lab.

‘At the time, we were looking for SARS-related viruses, and this one was 20 percent different,’ says Daszak. ‘We thought it’s interesting, but not high-risk. So we didn’t do anything about it and put it in the freezer.’

The group has found around 500 bat-borne viruses in China over the last 16 years, but only flagged those that most resembled SARS to the authorities – a lack of funding meant they couldn’t further investigate the virus strain now known to be 96 percent genetically similar to the virus that causes Covid-19.”

Interesting though that story is, it fails to explain how SARS-CoV-2 evolved. Some scientists say it would take 50 years5 for RaTG13 to turn into SARS-CoV-2. Others propose theories6 on how the virus might have evolved so quickly, yet still suspect that it escaped from the Wuhan lab.

Certainly, to learn that the closest known relative to SARS-CoV-2 has been in the care of the gain-of-function researchers at the Wuhan Institute of Virology (WIV) for seven years does nothing to allay suspicions that the virus infected humans only after being tinkered with in a lab.7

Still, the National Institute of Allergy and Infectious Diseases is going all-in on virus hunting. The institute just announced a five-year, $82-million8 investment in a new global network of Centers for Research in Emerging Infectious Diseases, including gain-of-function experiments to “determine what genetic or other changes make [animal] pathogens capable of infecting humans.”

Daszak’s EcoHealth Alliance will receive $7.5 million9 from this grant. This is on top of $100.9 million10 that EcoHealth Alliance has received in government grants and contracts since 2003. (What was that Daszak said about how “a lack of funding meant they couldn’t further investigate the virus strain now known to be 96-percent genetically similar to the virus that causes Covid-19”11)?

Critics12 of virus hunting say scientists like Daszak could make a greater contribution to human health by going after the viruses that commonly infect humans, not the ones that never have. According to a 2018 Smithsonian Magazine report:13

“Not everyone thinks that discovering viruses and their hotspots is the best way to prevent pandemics. Dr. Robert B. Tesh, a virologist at the University of Texas Medical Branch, says we don’t understand enough about zoonotic viruses to create predictive models. ‘A lot of the stuff they produce is hype. … It’s more PR than science.'”

Daszak’s research might be more hype14 and public relations than science, but the Department of Homeland Security’s National Biosurveillance Integration Center (NBIC) has chosen to rely on it. NBIC gave Daszak’s EcoHealth Alliance a $2.2-million15 contract (2016-2019) to create a “Ground Truth Network”16 of “subject matter experts” who could provide “contextual information pertaining to biological events.”

The context17 Daszak invariably provides is a compelling one. Destruction of forests and other encroachments on wildlife habitats, especially the hunting of wild animals and the sale of live animals in wet markets, is forcing humans and animals into uncomfortable proximity. This is bad for vulnerable and endangered species, as well as for humans who are at increasing risk for contracting novel zoonotic diseases.

Who isn’t shocked and appalled to learn that people eat bats, or that marvelously strange and adorable animals you’ve never heard of ― pangolins, civet cats ― have had their habitats destroyed and are now being sold for meat at live animal markets? Daszak’s framing of the issue ― what has come to be known as the One Health approach ― has been heartily embraced by the U.S. military.

But what if the stories being spun by Daszak and his fellow government-supported subject matter experts aren’t supported by the evidence? Let’s look at EcoHealth Alliance’s story about Ebola and bushmeat.

Click here to read more

False Narrative, Tragic Outcomes

From 2011 to 2014, Ecohealth Alliance had a $164,480 purchase order contract from the Centers for Disease Control in Pittsburgh for “Bushmeat.” No more information than that is available on that contract (HHSD2002011M41641P18), but the money likely funded a paper Daszak and his colleagues published in 2012.

The 2012 paper,19 “Zoonotic Viruses Associated with Illegally Imported Wildlife Products,” was used in August 2014, at the height of the West African Ebola pandemic, as the basis for a Newsweek article titled, “Smuggled Bushmeat Is Ebola’s Back Door to America.”20

The article, which quoted an EcoHealth Alliance spokesperson, spread a false (not to mention racist and xenophobic) narrative, one that subsequently would be thoroughly debunked,21 that bushmeat smuggled to the U.S. from Africa could transmit Ebola to Americans.

In January 2015, a meeting of the UK Bushmeat Working Group convened. The group countered Daszak’s misinformation with the facts, in an article titled, “Ebola and Bushmeat: Myth and Reality.”22 The article stated:

“As the Ebola virus can remain viable in untreated carcasses for up to 3-4 days, there is a risk of transporting it to bushmeat markets (although there is no evidence of this to date).

However, the risk of transmitting Ebola in bushmeat overseas to Europe or the USA is extremely low, given the total travel time and the fact that these carcasses are usually smoked (which probably inactivates the virus). The risk of spread to new areas lies with the movement of infected people, not infected meat.”

Tragically, the misinformation about bushmeat as a primary cause of Ebola transmission had already been communicated to West Africans in the midst of the crisis, through international health organizations, including Daszak’s funder,23 the U.S. Centers for Disease Control and Prevention (CDC).

Daszak’s misinformation campaign overshadowed the truth — that the only way Ebola was actually being transmitted during the pandemic was via contact with the bodily fluids of people sick with Ebola, or with their corpses.

Perpetuating Mythical Theories

The SARS pandemic is another instance where Daszak’s theories didn’t pan out. It is commonly accepted that the SARS pandemic began in 2002,24 when humans caught a bat virus from civet cats at a wet market in Guangdong, China. But Daszak and his collaborators admit they have no evidence to explain how the virus leapt from bats to civets to humans.

SARS-CoV was found in civets at the Guangdong wet market, but civets aren’t the natural reservoir of this virus. Bats are. Only the civets at the market — and no farm-raised or wild civets — carried the virus. None of the animal traders handling the civets at the market had SARS.

When Daszak and his collaborators at the WIV25 searched the cave in Yunnan for strains of coronavirus similar to human versions, no single bat actually had SARS. Genetic pieces of the various strains would have to be recombined to make up the human version. Adding to the confusion, Yunnan is about 1,000 kilometers from Guangdong.

So, how did viruses from bats in Yunnan combine to become deadly to humans, and then travel to civets and people in Guangdong, without causing any illnesses along the way during this 1,000 kilometer trip? No one knows. Just like no one knows how SARS-CoV-2, the virus that causes COVID-19, leapt from bats to pangolins to humans.

(The most recent study, “Broad host range of SARS-CoV-2 predicted by comparative and structural analysis of ACE2 in vertebrates”26 in the Proceedings of the National Academy of Sciences,27 showed that the SARS-CoV-2, which infects human cells through binding of the viral Spike protein to ACE2, has a “very high” binding affinity to ACE2 in “Old World” monkeys apes, and humans.

But in bats, the binding affinity is “low” and in pangolins it is “very low.” The authors also noted that “neither experimental infection nor in vitro infection with SARS-CoV-2 has been reported for pangolins.”)

Daszak continues to tell his bat-origin story,28 but the science doesn’t back it up. That ― along with the fact that dozens of labs conduct “gain-of-function”29 research on bat coronaviruses and there are troubling safety issues30 at these labs ― is why the National Institutes of Health (NIH) is investigating the possibility that SARS-CoV-2 escaped from a lab.

Inquiring Minds at the NIH Want to Know

On July 8, the NIH sent a letter31 to Daszak asking EcoHealth Alliance to arrange for an inspection of the WIV by an outside team that would examine the facility’s lab and records “with specific attention to addressing the question of whether WIV staff had SARS-CoV-2 in their possession prior to December 2019.”

The WIV and the Wuhan University School of Public Health are listed as subcontractors for EcoHealth Alliance under a $3.7-million NIH grant32 titled, “Understanding the Risk of Bat Coronavirus Emergence.”

The two institutions also worked as collaborators under another $2.6-million grant,33 “Risk of Viral Emergence from Bats,” and under EcoHealth Alliance’s largest single source of funding, a $44.2 million sub-grant34 from the University of California at Davis for the PREDICT project (2015-2020).

It’s the $44.2-million PREDICT grant that EcoHealth Alliance used to fund35 the gain-of-function experiment by WIV scientist Zhengli Shi and the University of North Carolina at Chapel Hill’s Ralph Baric.36

Shi and Baric used genetic engineering and synthetic biology to create a “new bat SARS-like virus … that can jump directly from its bat hosts to humans.” Daszak described the work being done by Shi and Baric in a 2019 interview:37

“You can manipulate them [coronaviruses] in the lab pretty easily. Spike protein drives a lot of what happens with the coronavirus, zoonotic risk. So, you can get the sequence, you can build the protein, and we work with Ralph Baric at UNC to do this. Insert it into a backbone of another virus, and do some work in the lab.”

The work, “A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence,”38 published in Nature in 2015 during the NIH’s moratorium39 on gain-of-function research, was grandfathered in because it was initiated before the moratorium (officially called the U.S. Government Deliberative Process Research Funding Pause on Selected Gain-of-Function Research Involving Influenza, MERS and SARS Viruses), and because the request by Shi and Baric to continue their research during the moratorium was approved by the NIH.

As a condition of publication, Nature, like most scientific journals, requires40 authors to submit new DNA and RNA sequences to GenBank, the U.S. National Center for Biotechnology Information Database. Yet the new SARS-like virus Shi and Baric created wasn’t deposited41 in GenBank until May 2020.

Why Stop With Wuhan?

NIH is right to require that the WIV’s lab and records be opened to outside inspectors. But why is the government focusing on just one of EcoHealth Alliance’s projects, when the organization has received $100.9 million42 in grants, primarily from the Department of Defense, to sample, store and study bat coronaviruses at labs around the world?

Coronaviruses, both those that have been collected from animals and those that have been created through genetic engineering and synthetic biology, at all of these labs should be compared with SARS-CoV-2.

Daszak’s collaborators working under contracts with the Department of Health and Human Services (HHS) aren’t allowed to conduct gain-of-function research unless specifically approved to do so by the Potential Pandemic Pathogen Care and Oversight (P3CO) committee. This committee was set up as a condition for lifting43 the 2014-2017 moratorium on gain-of-function research.

The P3CO committee operates in secret. Not even a membership list has been released. The only information provided to the public is that Assistant Secretary for Preparedness and Response Robert Kadlec44 appointed HHS Senior Science Advisor Christian Hassell45 as its chair.

It’s time to open the records of the PC3O committee’s deliberations and decisions to examine all gain-of-function research on coronaviruses. And every lab manipulating these viruses should have their coronaviruses compared to SARS-CoV-2.

The Pentagon’s Defense Threat Reduction Agency (DTRA) for its Cooperative Biological Engagement Program (now called the Biological Threat Reduction Program) isn’t supposed to fund gain-of-function (what they call “dual-use”46) research at all.

It’s time to determine whether this prohibition on “dual-use” funding has been adhered to, especially in light of the investments the Pentagon is making across the globe in the construction of new laboratories for the “consolidation and securing of pathogens.” DTRA’s mission was to dismantle the biological weapons programs of hostile or destabilized countries.

Instead it is being used to develop new biological weapons programs in dozens of countries around the world.

Even if these programs are purely defensive, they proliferate, around the globe, pathogens with pandemic potential, even though it’s been difficult to keep these dangerous germs under control here in the U.S. (See “The Global Proliferation of High-Containment Biological Laboratories: Understanding the Phenomenon and Its Implications,”47 and the Government Accountability Office’s reports, “Biological Select Agents and Toxins: Actions Needed to Improve Management of DOD’s Biosafety and Biosecurity Program,”48 and “High-containment Laboratories: Comprehensive and Up-to-Date Policies and Stronger Oversight Mechanisms Needed to Improve Safety”49).

EcoHealth’s Tentacles Reach Far and Wide

EcoHealth Alliance is very much involved in the Pentagon’s proliferation of high-containment biological laboratories. It is conducting DTRA-funded work in the following countries, which are all participants in the Pentagon’s Biological Threat Reduction Program.50

Tanzania — In Tanzania, a country that is considered only “partly free,”51 which has a history of foreign medical experimentation52 and which didn’t ratify the Biological Weapons Convention53 until 2019, EcoHealth Alliance has a $5-million Pentagon contract,54 “Crimean-Congo Hemorrhagic Fever: Reducing an Emerging Health Threat in Tanzania.”

Crimean-Congo Hemorrhagic Fever (CCHF)55 is a tick-borne disease, originally only infecting animals, that was discovered by Ottis and Calista Causey while working for the Rockefeller Foundation in Nigeria. There was only ever one case56 of CCHF in Tanzania, and that was in 1986.

Gain-of-function research57 on CCHF is being conducted at the U.S. Department of Agriculture’s National Bio and Agro-Defense Facility (NBAF) to determine the “mechanisms of CCHF transmission including development of CCHF tick and animal infection methods and CCHF tick-animal transmission models.” (The National Bio and Agro Defense Facility will take over the mission of the Plum Island Animal Disease Center and become the lead facility for Foreign Animal Disease research.)

The National Bio and Agro Defense Facility Biosafety Level 4 (BSL4) Zoonotic and Emerging Infectious Disease team’s CCHF Virus Surveillance Project58 is investigating “the interface between tick vectors, livestock and pastoralist and resource-poor farming communities in Tanzania” as well as the disease’s “molecular pathogenesis.”

Tanzania is the origin of chikungunya,59 a mosquito-borne virus that the U.S. has long cultivated60 as a potential biological weapon. according to a patent61 held by the University of Texas for a “chimeric” chikungunya virus created through genetic engineering and synthetic biology:

“The 39 documented laboratory infections reported by HHS in 1981 strongly suggest that Chikungunya virus is infectious via aerosol route. Chikungunya virus was being weaponized by the U.S. Army army when the offensive program was terminated.”

Tanzania is one62 of the countries where bat coronaviruses were collected for the PREDICT63 project. Tanzania has one Biosafety Level 3 (BSL3) laboratory, the privately owned Ifakara Health Institute,64 which is partnering with PREDICT65 to launch “concurrent surveillance of wildlife and people in at-risk areas for viral spillover and spread.”

South Africa — In South Africa, which had a notorious apartheid-era biological weapons program,66 EcoHealth Alliance has a $5-million Pentagon contract67 (2019-2024), “Reducing the Threat of Rift Valley Fever Through Ecology, Epidemiology and Socio-economics.” This is on top of a $4.9-million grant68 (2014-2019), “Understanding Rift Valley Fever in the Republic of South Africa.”

The last human outbreak69 of Rift Valley Fever in South Africa occurred in 2010, when the government reported 237 confirmed cases, including 26 deaths from nine provinces. But there were also a few cases70 in 2018 among farmworkers who slaughtered infected animals during an outbreak in livestock. The fever can spread from animals to humans if they come into contact with the blood and other body fluids of an infected animal.

The U.S. military has conducted offensive biological weapons research71 on Rift Valley Fever. South Africa’s biological weapons program72 included the weaponization of Rift Valley Fever virus obtained from the U.S. government.

Known as Project Coast, South Africa’s biological weapons program murdered anti-apartheid activists with narcotics and poisons, and attempted a genocide of the black majority by spreading AIDS73 and by developing pathogens and vaccines74 that would selectively attack black people with illness, death and infertility.

Dr. Wouter Basson,75 the project’s top scientist, told Pretoria High Court in South Africa that the U.S. Central Intelligence Agency threatened him with death, presumably to prevent him from revealing the deep connections between Project Coast and the U.S., which had forced President F. W. de Klerk to shut down the project and destroy its records.

Basson named the U.S. Centers for Disease Control as his source of eight shipments76 of Ebola, Marburg and Rift Valley viruses, but claimed that he had obtained the viruses by posing as a medical researcher and hiding his affiliation with the South African Defense Forces.

Surveys of bats in South Africa found no evidence77 of bats being natural carriers of Rift Valley Fever virus, but experiments have shown that bats can be infected78 with it in a laboratory setting.

A bat coronavirus collected79 in South Africa in 2011 was thought to be the closest known relative of the MERS-CoV virus that emerged in Saudi Arabia in 2012, until a 100-percent match for MERS-CoV was detected by Daszak and his colleagues in viral RNA fragments from an Egyptian tomb bat80 found near the home of one of the first MERS victims in Saudi Arabia.

Liberia — In Liberia, which didn’t ratify the Biological Weapons Convention until 2016,81 EcoHealth Alliance has a $4.91-million82 Pentagon contract,83 “Reducing the Threat from High-risk Pathogens Causing Febrile Illness in Liberia.” Febrile illnesses include Ebola, which has been the subject of some of the most controversial dual-use research.84

While the U.S. has a sordid history of biological weapons experimentation on its own people — with conscientious objectors,85 military “volunteers,”86 and the general public87 as frequent subjects — there were some biological weapons tests88 the Department of Defense considered too unethical to perform within the continental U.S. Those tests were conducted in other countries, including Liberia.89

Likewise, mirroring medical experimentation90 on African Americans, there is a history of colonial medical experimentation in Liberia going back to 1926 when the Firestone91 tire company financed surveys of local diseases they feared could curtail the profitability of their rubber plantations.

More recently, a failed Pentagon-funded Ebola drug trial92 caused many Liberians to suspect that the subsequent Ebola outbreak was the fault of Tekmira, the pharmaceutical company that created TKM-100802. Doubt surrounded the official story, promoted93 by Daszak, that the West African Ebola outbreak happened because bats flew in with the Ebola Zaire virus from 2,500 miles away.

In January 2014, the Phase I trial94 for TKM-100802 was launched, but put on clinical hold by the U.S. Food & Drug Administration due to high cytokine release in participants. In a dose-escalation, healthy volunteer study, one (of two) participants dosed at the highest level of 0·5 mg/kg experienced cytokine release syndrome.95

Cytokine release syndrome96 is a pro-inflammatory reaction that occurs when activated lymphocytes and/or myeloid cells release soluble immune mediators following administration of certain therapeutic agents, especially monoclonal antibodies. Onset can be rapid (within hours of administration) and can be life-threatening.

Ultimately, TKM-100802 proved useless97 for Ebola patients, but the Pentagon’s $140-million98 investment, and the boost99 Tekmira’s stock experienced on speculation that Ebola would soon spawn the next $1-billion drug,100 made many investors rich.

Suspicions were raised because the TKM-100802 Phase I trial on healthy volunteers began in January 2014, before101 the first cases of the Ebola outbreak in March 2014.

Later, the World Health Organization’s Pierre Formenty traced the first case102 back to late December 2013, in Meliandou, Guinea. There, 50 meters from the home of patient zero, another researcher, Fabian Leendertz,103 found DNA fragments that matched the Angolan free-tailed bat, a species known to survive experimental infections with Ebola.

Then, Daszak’s EcoHealth team found viral RNA fragments104 of Ebola Zaire in a greater long-fingered bat, captured in 2016 in Liberia’s Sanniquellie-Mahn District, which borders Guinea. There was a 1982 article105 in Annals of Virology in which a trio of Germans reported finding Ebola antibodies in 26 of 433 Liberians (6%). Bats aren’t the only place to look for Ebola.

There’s a BSL-4 lab that was handling Zaire Ebola before the pandemic in Kenema, Sierra Leone. This is where international law attorney Francis Boyle,106 a drafter of the U.S. Biological Weapons and Anti-Terrorism Act passed into law in 1981, believes the pandemic originated.

There’s also Liberia’s Monkey Island. As the Washington Post reported,107 that’s where 66 chimpanzees have been since 2004, when they were abandoned by the American scientists at the Liberian labs of the New York Blood Center. From 1974 to 2004, the New York Blood Center captured wild chimps, engaged them in medical experimentation and then released them back into the jungle in a project known as Vilab II108 (Virology Lab II), which maintained a colony of 200 chimps.

Vilab II was built from the remnants of the Liberian Institute of Tropical Medicine. Built by Firestone in 1946, the Liberian Institute of Tropical Medicine had once employed 60 scientists, but by 1974, medical doctor Earl Reber109 was there alone with eight chimps. The roots of the Liberian Institute of Tropical Medicine go back to the research begun in 1926 by Harvard Department of Tropical Medicine chief Richard Pearson Strong.

Virus hunters like Daszak should have a keen interest in a population of chimpanzees that, for nearly 100 years, has been caught, injected with viruses and then released back into the wild, especially considering the work of the researchers who handled the chimps.

The New York Blood Center is at the center of a theory110 on the origin of HIV/AIDS, that it came from a contaminated Hepatitis B vaccine the center distributed to gay men from 1978-1981. The New York Blood Center also tested111 its vaccine on Liberians.

Richard Pearson Strong112 is infamous for killing 13 men when he infected a group of 24 inmates of Manila’s Bilibid Prison with plague through a contaminated cholera vaccine. That was prior to his work113 in Liberia, which is only now being explored, and also involved experiments with humans as well as chimpanzees.

Georgia — EcoHealth Alliance has a $6.5-million Pentagon grant114 for “Understanding the Risk of Bat-borne Zoonotic Disease Emergence In Western Asia” (2017-2022).

Arms Watch115 reports that this grant involves genetic studies on coronaviruses in 5,000 bats collected in Georgia, Armenia, Azerbaijan, Turkey and Jordan. The studies were conducted at the Lugar Center, a $161-million Pentagon-funded biolaboratory in Georgia’s capital, Tbilisi. Russia claims116 the Georgia lab is the site of a U.S. biological weapons program.

According to USASpending.gov,117 EcoHealth Alliance has received $2.88 million in grants for work in Georgia. The Lugar Center is one of the labs that hosts EcoHealth Alliance’s Western Asia Bat Research Network.118

Malaysia — In Malaysia, which is only now in the process of creating a legislative framework119 for enforcing the Biological Weapons Convention, EcoHealth Alliance had a $1.6-million Pentagon grant120 (2017-2019) for “Serological Biosurveillance for Spillover of Henipaviruses and Filoviruses at Agricultural and Hunting Human Animal Interfaces in Peninsular Malaysia.”

There are no known cases of filovirus infections in humans in Malaysia. But Malaysia is the origin of the Nipah virus,121 first recognized in 1999, during an outbreak among farmers and farmworkers in factory farms and slaughterhouses producing pork.

The virus spread to Singapore. In all, there were 265 cases of acute encephalitis with 105 deaths, and the billion-dollar pig-farming industry nearly collapsed. No new outbreaks have been reported in Malaysia since 1999.

Nipah virus, a zoonotic pathogen for which no treatments exist, is the inspiration for the film “Contagion.”122 The virus can only be experimented on in BSL-4 laboratories. The National Bio and Agro-Defence Facility in Kansas will be the first biocontainment facility123 in the U.S. where research on Nipah and Ebola (a filovirus) can be conducted on livestock.

In 2019, Nipah Malaysia was among the deadly virus strains shipped124 from Canada’s National Microbiology Lab to the WIV. Henipaviruses,125 in the paramyxovirus family, were the first emerging diseases linked to bats.

In June 2012, in the same Chinese cave126 (actually an old copper mine where workers doing cleanup had become sick and died) in which Daszak’s WIV colleagues found SARS-CoV-2’s most closely related coronavirus, another frequent collaborator of Daszak’s, Zhiqiang Wu of the Chinese Academy of Medical Sciences, found a new henipavirus-like pathogen in a rat, naming it the “Mojiang paramyxovirus,”127 after the county in Yunnan province where it was found.

Malaysia was the planned site of a BSL-4 laboratory run by the pharmaceutical company Emergent Biosolutions128 for the production of a halal version of the BioThrax vaccine. But that project failed.129

In addition to the Pentagon funding, Dazsak obtained $1.7 million in grants130 (2002-2005) from NIH’s Fogarty International Center for “Anthropogenic Change & Emerging Zoonotic Paramyxoviruses.” In 2012-2014, Daszak had a $569,700 grant from the National Fish and Wildlife Service for “Development of a Great Ape Health Unit in Sabah, Malaysia.”

Daszak has a new National Institute of Allergy and Infectious Diseases grant,131 “Understanding Risk of Zoonotic Virus Emergence in EID Hotspots of Southeast Asia,” for $1.5 million (2020). The grant is for an “Emerging Infectious Diseases – South East Asia Research Collaboration Hub (EID-SEARCH)” that “brings leaders in emerging disease research from the U.S., Thailand, Singapore and the three major Malaysian administrative regions together to build an early warning system to safeguard against pandemic disease threats. This team will identify novel viruses from Southeast Asian wildlife [and] characterize their capacity to infect and cause illness in people …”

Other Pentagon Contracts

EcoHealth Alliance had a $1-million Pentagon contract132 (2017-2019) for an Inbound Bio-event Information System (IBIS), “a web-based application and early warning system for global infectious disease bio-events that threaten the U.S. via international transportation networks.”

EcoHealth Alliance also had another $4.5-million Pentagon contract (HDTRA115C0041133) for 2015-2017. No other information is available on this contract other than that it is for “Applied Research/Exploratory Development” in the “Physical, Engineering, and Life Sciences (except Biotechnology).”

Department of Homeland Security Contracts — EcoHealth Alliance has a $566,300 contract (2019-2021) with the Department of Homeland Security for the Rapid Evaluation of Pathogens to Prevent Epidemics in Livestock (REPEL) project134 “to apply biological-based, pathogen agnostic medical countermeasure vaccine and diagnostic platforms to develop foreign animal and emerging zoonotic livestock disease vaccines.”

Department of Health and Human Services Funding — Daszak obtained a $300,000-grant135 in 2012 from NIH’s Fogarty International Center for research on “Comparative Spillover Dynamics of Avian Influenza In Endemic Countries.” While most of the research listed in the “results” section of the grant are flu-related, it also includes the WIV’s paper,136 “Isolation and Characterization of a Bat SARS-like Coronavirus that Uses the ACE2 Receptor.”137

Daszak was given $3.7 million in grants138 (2002-2012) from NIH’s Fogarty International Center for “The Ecology, Emergence And Pandemic Potential of Nipah Virus in Bangladesh.”

The grants Daszak used to support the work of the WIV were a $3.7-million grant139 (2014-2020) “Understanding the Risk of Bat Coronavirus Emergence,” and a $2.6-million grant140 (2008-2012) “Risk of Viral Emergence From Bats,” each from the National Institute of Allergy and Infectious Diseases.

U.S. Agency for International Development (USAID) Funding

In Thailand, EcoHealth Alliance has a $647,200-grant141 for “One Health Workforce – Next Generation” (2019-2020).

Alexis Baden-Mayer is political director for the Organic Consumers Association (OCA). www.organicconsumers.org To keep up with OCA’s news and alerts, sign up here.

– Sources and References

Popular Prescription Will Increase Your COVID Hospital Stay


Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2020/09/16/popular-prescription-lengthens-hospital-stays.aspx
Analysis by Dr. Joseph Mercola    Fact Checked    September 16, 2020

prescription lengthens hospital stays

STORY AT-A-GLANCE

  • One study showed remdesivir lowered hospital days by 30%, yet doctors in Florida are finding that people who take the drug are staying longer than those who don’t
  • The company priced the drug based on how much it could save in hospital costs. The cost to produce, package and ship one vial is $10, while the commercial price is $520 per vial
  • Big Pharma is poised to make large profits from drugs and vaccines that the U.S. government subsidized during the COVID-19 pandemic
  • I believe it is crucial that you proactively support your immune system and not wait for a drug or vaccine with unknown, potentially long-term side effects. Optimizing your vitamin D is likely the easiest, least expensive and most beneficial strategy

In early 2020, a global pandemic spurred the world into action, especially in the science community. Researchers began seeking to discover how the COVID-19 virus worked and to uncover the best methods for testing, treating and vaccinating. One of the interventions that the biomedical community has been pursuing is the use of antivirals, including remdesivir.

The drug was initially analyzed during the Ebola outbreak several years ago but never approved. Its development was the result of a collaboration involving Gilead Sciences, the CDC and the U.S. Army Medical Research Institute of Infectious Diseases.

Testing was also done on SARS and MERS, which are both zoonotic coronaviruses, as well as two types of common human coronavirus which trigger the common cold. The medication was developed with a $99 million grant from the American government.1 A 2017 report noted that the Department of Defense “… is cost-sharing with Gilead biosciences for continued development of this product.”2

At the time it was labeled GS-5734.3 The initial studies that Gilead used to demonstrate the effectiveness of the drug had problems with the way they were designed, and changes made during the study would have negated the results.

Del Bigtree from Highwire, who serves as CEO of the Informed Consent Action Network, described the issues with the studies in detail, which you can read about at “Remdesivir Treatment Stopped Due to Side Effects.”

However, as just one of many technology platforms censoring or eliminating accounts that do not share the corporate view, YouTube terminated Bigtree’s entire account. This severing of information from public view has earned YouTube the title of “ministry of information” by some, because it infers that only YouTube/Google knows what’s right and wrong, according to user posts.4

Remdesivir Lengthens Hospital Stays for Some

As described in one study published in The Lancet, scientists conducted a randomized, double-blind, placebo-controlled investigation at 10 hospitals in China5 from February 6, 2020, to March 12, 2020.

Two-hundred thirty-seven people were enrolled and randomly assigned to either a treatment group or a placebo group. The results showed that remdesivir was not associated with statistically significant clinical benefits, and had to be stopped early because it was believed to have caused adverse events.

Despite a lack of strong evidence that the drug is beneficial, it is being used globally. In a highly quoted study about the drug, it was purported that it may have shortened hospital stays by 31%, from 15 days to 11.6

Dr. George Ralls with Orlando Health reports they are seeing positive benefits with remdesivir.7 However, he is also attributing a lengthier hospital stay to the need to complete a course of remdesivir. Interestingly, he also said the drug is keeping people in longer than if they weren’t taking the drug:

“Once they start on this medication … they need it for five days, so they are in the hospital longer than they would have normally been. So that could be a reason why our inpatient numbers have ticked up a little.”

It does not appear, then, that the drug is shortening hospital stays.

Click here to read more

Alternatives Are Available, but Ignored

In a paper from Dr. Harvey Risch of the Yale School of Public Health, published in the American Journal of Epidemiology, the use of hydroxychloroquine and azithromycin was cited as necessary to helping halt the pandemic.

The combination of inexpensive medications is highly effective during the first phase of the infection, before hospitalization. This does not compete with the intravenous drug remdesivir, used only after a person is hospitalized. Risch noted:8

“Remdesivir has shown mild effectiveness in hospitalized inpatients, but no trials have been registered in outpatients. Hydroxychloroquine+azithromycin has been widely misrepresented in both clinical reports and public media, and outpatient trials results are not expected until September. Early outpatient illness is very different than later hospitalized florid disease and the treatments differ.

Five studies, including two controlled clinical trials, have demonstrated significant major outpatient treatment efficacy. Hydroxychloroquine+azithromycin has been used as standard-of-care in more than 300,000 older adults with multicomorbidities … These medications need to be widely available and promoted immediately for physicians to prescribe.”

According to Global Research, the same protocol is showing significant success in China, India, Senegal and Brazil.9

As I have also written, French microbiologist and infectious disease expert Didier Raoult, director of a research unit at Institut Hospitalo-Universitaire in France, has reported that using a combination of hydroxychloroquine and azithromycin, administered immediately upon diagnosis in 1,061 people, led to recovery and “virological cure” in 91.7% of patients.10

It is also important to note that unlike remdesivir — which has had side effects severe enough to stop clinical trials — the hydroxychloroquine/azithromycin combination showed no cardiac toxicity, rhythmic cardiac events or sudden death in patient data.

$3,120 Five-Day Remdesivir: A ‘Spectacularly Good Value’

The long-awaited price for remdesivir was announced June 29, 2020, by Gilead Sciences. As reported in NPR, there was “months of speculation as the company tried to figure out how to balance profit and public health needs in the middle of a pandemic.”11 Daniel O’Day, chairman and CEO of Gilead Sciences, published an open letter in which he said:12

“Remdesivir, our investigational treatment, is the first antiviral to have demonstrated patient improvement in clinical trials for COVID-19 and there is no playbook for how to price a new medicine in a pandemic.”

While the drug has demonstrated only questionable benefits, O’Day is correct in saying there are no guidelines on pricing a new medicine in a pandemic. Yet, he believes Gilead balanced corporate profits and public health when they settled on $520 per vial, which equates to $3,120 for the recommended five-day course of treatment (on the first day, a double dose is given).

The Institute for Clinical and Economic Review (ICER) released the calculated total cost of production, packaging and a small profit margin May 1, 2020. The cost was rounded to $10 per vial.13

The same group noted that the company could charge a much higher rate depending on its effectiveness, with Dave Whitrap from ICER qualifying that statement by saying, “If the drug doesn’t impact mortality and only shortens recovery time, we figure a course of treatment is worth about $310.”14 Gilead is currently charging $2,810 more for a drug that has already proven it doesn’t reduce mortality.15

O’Day wrote that under “normal circumstances” a medication would be priced “according to the value it provides.”16 In this case they estimated that early discharge from the hospital would save approximately $12,000 per patient.

They believe the $3,120 price tag does not hinder anyone from receiving treatment, while it balances their responsibilities to continue work on remdesivir and research on antivirals.

High Level Coronavirus Profiteering

When the price for the drug was announced, an analyst for SVB Leerink, which is an investment bank, described the price as a “spectacularly good value.” The analyst, Geoffrey Porges, added that it is “unprecedented to price the drug below the medical costs that it’s saving.” He believes remdesivir has the potential to save $40,000 per patient by preventing someone from entering the ICU.

He also believes there’s more value that Gilead has not built into their price. In other words, a drug that taxpayers poured $99 million into the development of, and for which Gilead pays $10 per vial ($60 per course of treatment) to produce, is somehow underpriced at $3,120 for a single course of treatment.17

Using this same logic, a florist could base the charge for a dozen red roses on how much they save a couple by preventing the cost of a divorce. However, in the same way the florist does not know if flowers are for a celebration or an apology, Gilead has priced remdesivir on the assumption that patients will be hospitalized for four fewer days, even though Ralls finds that his patients who take the drug are actually in the hospital longer.

This is not the first time Gilead has leveraged exorbitant markups on their products. Sovaldi was billed as a “groundbreaking” drug to treat hepatitis C, for which Gilead charges $84,000 for each course of treatment.18 While some see the price for remdesivir as reasonable, it’s important to remember that drug production is nearly riskless for Big Pharma as they are often subsidized by the government.19

U.S. Rep. Lloyd Doggett, D-Texas, has been outspoken about the profits the pharmaceutical industry and others are making off the pandemic, saying, “The power of the industry combined with fear is driving extraordinary spending. It all suggests rosy times ahead for the pharmaceutical industry.”20

Big Pharma Poised to Make Big Profits

The profiteering has started for Gilead, which has a market capitalization of $90 billion21 and developed their antiviral drug with the help of your tax dollars. The day after the price was announced, the U.S. government bought 500,000 doses. Press secretary Kayleigh McEnany said this was so patients would not be charged the real cost of the drug.

On the surface, this means individuals will not be charged, yet all Americans are paying with their tax dollars. Emergency vaccine spending bills were recently passed, allocating $6 billion for manufacturing and distribution and $20 billion for development.

As Doggett points out, “The public will pay for much research and manufacturing. Only the profits will be privatized. We’re in the extraordinary position of spending billions on vaccines before we know if they work.”22

Rolling Stone reports that some large pharmaceutical companies have made pledges regarding the cost of future vaccines, including Johnson & Johnson and AstraZeneca. Astra Zeneca CEO Pascal Soriot announced, “We’ll do it at no profit.”23

Yet, when Doggett and his staff contacted the drug companies for clarification about what their statements meant, they did not get an answer, nor was there definition of “cost” included. Gestures like this may look good in the news but only time will tell if they keep their promises.

Without announcing an end date and knowing that many public health experts will be pushing a vaccine for many years, it’s highly unlikely that any pharmaceutical company will provide a drug at cost for more than a short time to meet the initial need.

Healthy Choices That Make a Difference

Some public health officials and the media are wringing their hands over the number of new cases being diagnosed each day. Using these numbers to generate fear and distress, they encourage people to stay in place and wait for a vaccination.

However, I recommend that you take a proactive approach in supporting your immune system. There are a number of simple, yet significant strategies you can use that you’ll find on my Coronavirus Resource Page.

It has become more apparent with every passing week that optimizing your vitamin D level is likely the easiest, least expensive and most beneficial strategy you can use to minimize your risk.

The best time to start addressing your vitamin D level is right now, before the second wave of disease that health officials expect in the fall. You’ll find more information about the importance of vitamin D and how the body uses it to combat coronavirus and other infectious diseases in “The Most Important Paper Dr. Mercola Has Ever Written.”

It is my hope you use this resource to spread the word about the significance of vitamin D to your friends and family. Within the report I go into detail about how to raise your levels between 60 ng/mL and 80 ng/mL.

One important first step is to get your vitamin D level tested so you know where to start. You’ll find a quick summary of the key steps and information about getting tested in the article linked above.

Global Uprising Underway


Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2020/09/16/global-uprising.aspx
Analysis by Dr. Joseph Mercola    Fact Checked    September 16, 2020

STORY AT-A-GLANCE

  • After six months of intermittent or in some cases near-continuous lockdowns, many have reached their limit and uprisings are finally emerging around the world
  • The last week of August 2020 saw gatherings of tens of thousands of individuals in Berlin, London and Dublin, protesting stay-at-home orders, business closures, mask and vaccine mandates and Bill Gates’ dictatorial grip on public health matters
  • According to data released by the U.S. Centers for Disease Control and Prevention August 26, 2020, only 6% of the total COVID-19-related deaths in the U.S. had COVID-19 listed as the sole cause of death on the death certificate
  • A September 2, 2020, study found the overall noninstitutionalized infection fatality ratio was 0.26%. Among those under the age of 40, the infection fatality ratio is 0.01%, while those over 60 have an infection fatality ratio of 1.71%
  • The estimated infection fatality rate for seasonal influenza is 0.8%, so the only people for whom SARS-CoV-2 infection is more dangerous than influenza are those over the age of 60. Everyone else has a lower risk of dying from COVID-19 than they have of dying from the flu

After six months of intermittent or in some cases near-continuous lockdowns, many have reached their limit and uprisings are finally emerging around the world. The last week of August 2020 saw gatherings of tens of thousands of individuals in Berlin,1 London2 and Dublin,3 protesting stay-at-home orders, business closures, mask and vaccine mandates and Bill Gates’ dictatorial grip on public health matters.

In the U.S., a protest took place August 30, 2020, in Boston, Massachusetts, against a new student flu vaccination mandate,4 and in Virginia, protesters gathered September 2 in opposition of unconstitutional COVID-19 mandates.5

These are just a few of the many demonstrations that have taken place in recent weeks around the world, as people are starting to realize their human rights are being stripped away over a virus with a lethality on par with that of seasonal influenza and other pandemic viruses, none of which was responded to with a global shutdown of economies and forced quarantining of healthy individuals.

COVID-19 — A Massive Brainwashing Scheme?

In recent weeks and months, more and more experts have come out sharing what they know about the roles of Big Tech, Big Pharma and global health organizations such as the World Health Organization in the creation of a new technocratic world order.

If you missed my interview with financial analyst Patrick Wood, in which he details the technocratic take-over plan, which has been in play for decades, be sure to review it now. Other articles shedding light on what’s happening behind the scenes include “Harvard Professor Exposes Google and Facebook,” featuring a documentary with professor Shoshana Zuboff, and “Plandemic Part 2.”

When you start to put all the puzzle pieces together, it seems clear this pandemic is being used as a cover story for both a global wealth redistribution scheme, and for the implementation of a technocratic system of totalitarian rule by unelected leaders.

The WHO seems to be part and parcel of this global network. While the U.S. has severed ties with the organization, Big Tech is still promoting the WHO as a final arbiter of which views are acceptable and which are not — medical expertise and scientific achievements be damned.

As reported by Reclaim the Net,6 the WHO eavesdrops on everything you do online, from reviewing your social media interactions to analyzing your emotions. To counteract “spread of misleading information” about the pandemic — which was a key area of focus during Event 201 — the WHO has partnered with an analytics company that uses machine learning analysis to scan more than 1.6 million social media posts per week.

The aim of this “social listening approach”— a nicer term than good old-fashioned spying — is to counteract anything that doesn’t align with the WHO’s current narrative on illnesses, treatments, interventions and causes of disease.

Aiding them in this dystopian censoring process is the United Nations, which has launched an army of 10,000 digital volunteers who troll the internet for “false” information and opposing views.

On top of that, most social media platforms have their own highly biased “fact-checkers” who censor for all they’re worth. Back in April 2020, YouTube CEO Susan Wojcicki, wife of Google product director Dennis Troper, announced they would ban and remove any video from the platform that contradicts the WHO.7

Countless examples of wanton censorship of perfectly valid medical and scientific information across all social media platforms and Google can be found at this point.

Click here to read more

Just How Deadly Is COVID-19?

According to groundbreaking data8 recently released by the U.S. Centers for Disease Control and Prevention, only 6% of the total COVID-19-related deaths in the U.S. had COVID-19 listed as the sole cause of death on the death certificate.

Six percent of 169,044 (the total death toll as of September 2) is 10,143. “For deaths with conditions or causes in addition to COVID-19, on average, there were 2.6 additional conditions or causes per death,” the CDC states. As reported by Rochester First,9 the top underlying medical conditions included influenza, pneumonia, respiratory failure, high blood pressure, diabetes, dementia, heart problems and renal failure.

However, the list also includes 5,424 intentional and unintentional injury and poisoning deaths, so basically, accidents and suicides in which the individual just happened to test positive (or was suspected of being positive for SARS-CoV-2) are also included in the grand total.

(Please note, these data were accurate as of this writing. The CDC does not notate when data is altered as new death certificates come in, so the numbers may therefore be different from what is reported here, depending on when you’re looking at it. For the most up-to-date figures, see the CDC’s website.10)

The fact that only 6% of COVID-19-related deaths are directly attributable to SARS-CoV-2 is bad news when you’re trying to keep a doomsday narrative going. In what appears to be a blatant attempt to minimize exposure of these data, social media platforms have censored many trying to share it.11

As noted by independent news commentator Tim Pool in the video below, fact-checkers are digging into nitpicky semantics in their effort to censor the CDC data, and in so doing, they’re really stretching the “false” claim ultrathin.

Similar data have emerged from Palm Beach County, Florida, where an investigation by CBS 1212 I-Team revealed only 86 of the reported 658 COVID-19 deaths had “COVID-19 pneumonia” listed as the sole cause of death.

All others had multiple comorbidities, including diabetes, cardiovascular diseases and dementia. As noted by CBS 12, “Most Palm Beach County COVID deaths cannot be attributed to COVID alone.”

While Dr. Terry Adirim, senior associate dean at the Florida Atlantic University College of Medicine, told the I-Team that “it makes sense to count them [people with comorbid conditions] toward COVID deaths because the virus may have made an otherwise nonfatal illness like a heart condition deadly,” the converse argument can also be made.

Had it not been for them having one or more serious comorbidities, the risk of the virus to these individuals would have been minuscule, and if they got sick at all, they’d probably have survived. So, ultimately, should the virus bear the brunt of the blame?

Infection Fatality Rate on Par With the Flu

Keeping the “killer virus” narrative going much longer is probably going to become even more difficult in light of a September 2, 2020 article13 in Annals of Internal Medicine, which points out that:

“Because many cases of coronavirus disease 2019 (COVID-19) are asymptomatic, generalizable data on the true number of persons infected are lacking, and that when calculating mortality rates from confirmed cases, you end up overestimating the infection fatality ratio (IFR).”

The paper reads, in part:14

“To calculate a true infection fatality ratio, population prevalence data are needed from large geographic areas where reliable death data also exist … We combined prevalence estimates from a statewide random sample with Indiana vital statistics data of confirmed COVID-19 deaths.

In brief, our stratified random sample consisted of state residents aged 12 years and older. Known decedents and incarcerated persons were excluded. Because nursing homes were limiting residents’ ability to leave and re-enter the facilities, their participation was unlikely.

Participants were tested from 25 April to 29 April 2020 for active viral infection and SARS-CoV-2 antibodies, which would indicate prior infection … We calculated the IFR by age, race, sex, and ethnicity on the basis of the cumulative number of confirmed COVID-19 deaths as of 29 April 2020, divided by the number of infections.

Although nursing home residents were not tested, they represented 54.9% of Indiana’s deaths. Thus, we excluded nursing home residents from all calculations (that is, deaths and infections).

To account for all infections, we added the number of patients hospitalized with COVID-19 during the testing period and noninstitutionalized COVID-19 deaths into the denominator …

Our random-sample study estimated 187 802 cumulative infections, to which 180 hospitalizations were added. The average age among all COVID-19 decedents was 76.9 years.

The overall noninstitutionalized infection fatality ratio was 0.26% … Persons younger than 40 years had an infection fatality ratio of 0.01%; those aged 60 or older had an infection fatality ratio of 1.71%. Whites had an infection fatality ratio of 0.18%; non-Whites had an infection fatality ratio of 0.59%.”

The estimated infection fatality rate for seasonal influenza listed in this paper is 0.8%. So, the only people for whom SARS-CoV-2 infection is more dangerous than influenza is those over the age of 60.

All others have a lower risk of dying from COVID-19 than they have of dying from the flu. Put another way, if you’re under the age of 60, your chances of dying from the flu is greater than your chance of dying from COVID-19.

White House coronavirus task force coordinator Dr. Deborah Birx also confirmed this far lower than typically reported mortality rate when she, in mid-August 2020, stated that it “becomes more and more difficult” to get people to comply with mask rules “when people start to realize that 99% of us are going to be fine.”15

Expect Massive Propaganda Campaign to Boost Vaccine Uptake

With death rates being as low as they are for everyone under the age of 60, it really weakens the rationale for vaccinating the entire world, including newborns, the risk to whom the virus poses is virtually nil.

The vaccine looking increasingly unnecessary is likely a reason for why the U.S. government is planning to launch an “overwhelming” COVID-19 vaccine campaign this fall, using carefully researched messages. As detailed in “Health and Autonomy in the 21st Century,” Yale University has conducted a trial16 to determine the type of message that will maximize acceptance and uptake of the COVID-19 vaccine. Messaging slants evaluated in the investigation included:17

Personal freedom message — A message about how COVID-19 is limiting people’s personal freedom and how working together to get enough people vaccinated can preserve society’s personal freedoms.
Economic freedom message — A message about how COVID-19 is limiting people’s economic freedom and how, by working together to get enough people vaccinated, society can preserve its economic freedom.
Self-interest message — A message that COVID-19 presents a real danger to one’s health, even if one is young and healthy, with the idea being that getting vaccinated against COVID-19 is the best way to prevent oneself from getting sick.
Community interest message — A message about the dangers of COVID-19 to the health of loved ones. The idea to promote is that the more people who get vaccinated against COVID-19, the lower the risk that one’s loved ones will get sick. The idea: Society must work together and all get vaccinated.
Economic benefit message — A message about how COVID-19 is wreaking havoc on the economy and the only way to strengthen the economy is to work together to get enough people vaccinated.
Guilt message — This message is about the danger that COVID-19 presents to the health of one’s family and community, with the idea that the best way to protect them is by getting vaccinated, and that society must work together to get enough people vaccinated. Then it asks the participant to imagine the guilt they will feel if they don’t get vaccinated and spread the disease.
Embarrassment message — This message is about the danger that COVID-19 presents to the health of one’s family and community. The idea to promote is that the best way to protect them is by getting vaccinated and by working together to make sure enough people get vaccinated. Then it asks the participant to imagine the embarrassment they will feel if they don’t get vaccinated and subsequently spread the disease.
Anger message — This message is about the danger that COVID-19 presents to the health of one’s family and community. The sales idea is that the best way to protect them is by getting vaccinated and by working together to make sure that enough people get vaccinated. It then asks the participant to imagine the anger they will feel if they don’t get vaccinated and spread the disease.
Trust in science message — A message about how getting vaccinated against COVID-19 is the most effective way of protecting one’s community. It promotes the idea that vaccination is backed by science, and that anyone who doesn’t get vaccinated doesn’t understand how infections are spread or who ignores science.
Not bravery message — A message which describes how firefighters, doctors and front line medical workers are brave, and infers that those who choose not to get vaccinated against COVID-19 are not brave.

The study, which was completed July 8, 2020, also sought to determine:

  • Participant’s confidence in the safety and effectiveness of the vaccine after hearing the message in question
  • Participant’s willingness to persuade others to get vaccinated
  • Their fear of those who have not been vaccinated
  • The social judgment of those who choose not to vaccinate

Prosocial Pressure Tactics Work Best

Harvard Business School in collaboration with the Sloan School of Management, Massachusetts Institute of Technology, have also published a working paper18 comparing self-interested versus prosocial motivations for COVID-19 prevention behaviors.

Considering the messages we’ve been bombarded with over the past few months — calling people who don’t wear masks “grandma killers” and so on — it seems clear that results from these kinds of investigations have been capitalized on.

In that paper, “Don’t Get It or Don’t Spread It?” the authors review studies in which various types of messages were compared — messages highlighting the threat to self, versus the threat you might pose to others.

Overall, prosocial messages, i.e., messages that stress the importance of complying with prevention behaviors in order to protect others fared the best. According to the authors:19

“These results reveal that prosocial framing was more effective than self-interested framing, suggesting a potential primacy of prosocial motivations in supporting prevention intentions …

First, prosocial framing may have been relatively more effective not because prosocial motivations do more to drive prevention intentions, but rather because people believe that COVID-19 poses a greater threat to society than to themselves.

Indeed, subjects in Studies 1-2 did on average report that coronavirus posed a larger public than personal threat.

However, we find that the advantage of the Public treatment (relative to the Personal treatment) was not significantly moderated by ‘threat difference scores’ (i.e., differences between the reported personal vs. public threat of coronavirus), or significantly smaller among subjects who reported the personal threat of coronavirus to be as large or larger than the public threat …

Thus, we find evidence that the relative effectiveness of the Public treatment was not unique to subjects who saw COVID-19 as more threatening to society than to themselves.

A second possibility is that prosocial framing (which encourages people to avoid spreading coronavirus) was more effective than self-interested framing (which encourages people to avoid getting coronavirus) because people feel relatively more empowered to avoid spreading the virus.”

Stop Believing in the Lockdown

A powerful essay20 in the American Institute for Economic Research asks the question: Is the lockdown the best way to minimize casualties in this pandemic?

Using historical examples beginning with Voltaire’s words, “those who can make you believe absurdities, can make you commit atrocities,” the author reasons that lockdowns are not going to save the world from COVID-19, if for no other reason than whenever lockdowns are eased, infections naturally start to creep back up.

However, the vast majority of these “infections” or “cases” are asymptomatic. A rising “case” load does not mean people are actually getting sick and dying. The misuse of the medical term “case” is an egregious one, as historically, a “case” is defined as someone who has symptoms of a particular disease — someone who is actually sick.

Never in medical history has a “case” meant someone who is perfectly healthy and requires testing to determine whether they are infected with a particular pathogen. Would you get tested for the common cold or influenza if you had no symptoms? If the test happened to come back positive, would you with a straight face say you “have” a cold or the flu?

There are other myths, mostly scare tactics, that people are willingly believing that need to be stopped now, too, the author asserts — and it’s time to start questioning what is credulous and what is not. I encourage you to read that essay in its totality.

The Fatal Attraction of Techno-Fascism

Another article21 well worth reading is Mark Petrakis’ “The Fatal Attraction of Techno-Fascism.” This one also starts off with an excellent quote by Cato the Elder: “Those who are serious in ridiculous matters will be ridiculous in serious matters.” One of the first points he makes is that fascism is attractive because:

“… it requires so little from us, so little independent thought; just our basic belief and adherence to a limited set of popularly-shared directives and narratives that once fully accepted, relieve us of the need to address stubborn questions or to fret over subtle differences of opinion and feeling.

Propaganda reassures us that we are complete, that we know all there is to know, that we are rational, pragmatic and pure, that the science has been settled and that we are a part of something special.”

Petrakis goes on to discuss why propaganda and disinformation is required in order to maintain control in a fascist regime, and how truth is a liability that must be disallowed and penalized. In the end, the price we pay for this kind of intellectual laziness is “soul-crushing denial and disconnection.”

No one who has been paying attention this past year in particular can have missed that propaganda is in full swing, 24/7, and that both truthful facts and personal opinions that run counter to the established propaganda narrative are being censored and penalized in equal measure.

When it comes to COVID-19, the propaganda is so pervasive and widespread that it has actually shattered what Petrakis refers to as “the grandest illusion of all” that “must be maintained at all costs,” namely the appearance that the propaganda messages are randomly generated.

“It must always appear that the media’s coverage and the comments of experts are entirely free from any preconceived manipulation,” he says. Today, there is little doubt that the narrative we see is anything but free from bias. There’s little doubt that what we’re told is “weaponized storytelling,” to quote Petrakis yet again.

“Looking at our world, we can see that the reach and authority of the transnational global capitalists who run the world’s nation-sized casinos has been cemented. All systems are now in place, up and running LIVE on that criminal syndicate’s vast web of networks. Each one of us has by now been targeted by them for some form of surveillance and financialization …

The ‘A.I. control grids’ are all active and expanding. The technocratic agendas are now fully ready for prime-time.

We have been gradually ‘shepherded’ by propaganda and psychological torture techniques … under the ‘persistent’ control of A.I., which will guide the process of transmuting us into commodities, into plunderable assets, into digitally-regulated and genetically modified ‘livestock.’ Sadly, this is where decades of constant acquiescence to propaganda and institutional hypnosis has brought us …”

Ultimately, the economic system known as technocracy is tailor-made for the transhumanist revolution — which I touch upon in “Will New COVID Vaccine Make You Transhuman?” — where man is merged with technology and AI. As always, the lure will be greater convenience, self-improvement and “a better world for all.”

What’s never mentioned is the ultimate price. The price for all of it is complete subjugation to faceless leaders who profit from your every move, and therefore will dictate all of them.

COVID-19 Rules Mark ‘Hysterical Slide Into Police State’

I’ll end this with some observations by British Supreme Court judge Lord Sumption, who in a March 30, 2020, interview22 with The Post warned that COVID-19 rules are paving the way for despotism — the exercise of absolute power in a cruel and oppressive manner.

“The real problem is that when human societies lose their freedom, it’s not usually because tyrants have taken it away. It’s usually because people willingly surrender their freedom in return for protection against some external threat. And the threat is usually a real threat but usually exaggerated.

That’s what I fear we are seeing now. The pressure on politicians has come from the public. They want action. They don’t pause to ask whether the action will work. They don’t ask themselves whether the cost will be worth paying. They want action anyway. And anyone who has studied history will recognize here the classic symptoms of collective hysteria.

Hysteria is infectious. We are working ourselves up into a lather in which we exaggerate the threat and stop asking ourselves whether the cure may be worse than the disease.”

It is time to ask ourselves some very pressing questions. Is it reasonable to expect government to eliminate ALL infection and ALL death? They’ve proven they cannot, yet we keep relinquishing more and more freedoms and liberties because they claim doing so will keep everyone safer. It’s an enticing lie, but a lie nonetheless.

Remember, they sold us on the business shutdowns and home quarantining by saying we just need to flatten the curve of infection to avoid hospital overcrowding. Now the curve is in a visible nosedive and hospitals are far from overcrowded with COVID-19 patients, yet lockdowns remain in many areas and some — Australia being a prime example — have reached astonishing new heights.

Sooner or later everyone must decide which is more important: Personal liberty or false security? Circling back to where I started, the good news is that many are in fact starting to see the writing on the wall; they’re starting to see we’ve been “had,” and are starting to choose liberty over brutal totalitarianism in the name of public health.

Community and World United, We Say No!

© 14th September 2020 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc.
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Your donation will help to support us in our efforts.
Reproduced from original article:
childrenshealthdefense.org/news/community-and-world-united-we-say-no SEPTEMBER 14, 2020


Children’s Health Defense is proud to stand with all of these organizations and countries (below) as we work together to pushback on medical mandates, unsafe vaccines, and increasingly totalitarian governments.

In the coming months, these issues will be front and center in discussions around the world as people decide whether to cling tightly to their freedoms or blindly follow whatever edicts are put in place by corrupt government officials and profit-driven corporations.

The making of this video was accomplished through the teamwork of organizations and individuals who will not stand by and watch liberty be stripped away from citizens little by little until total tyranny reigns.

Please join us in standing up and demanding that our individual and medical freedom rights are forever protected. The time to be courageous is now.

#WeSayNo   #StandFirm

(See Full Script Below)

 

Organizations in Unity:

(Please send us a “General” email from our Contact Us page if you would like to add your organization name)

Children’s Health Defense
The Institute for Pure and Applied Knowledge
The Bolen Report
GreenMedInfo
Autism Action Network
DeMoss Chiropractic
California Jam
Health Choice 4 Action
Northport Wellness Center
Natural News 
Dr. Northrup.com
Medical Freedom Pac
The Truth About Cancer
The Truth About Vaccines
1986 The Act Movie
Informed Consent Action Network
National Vaccine Information Center
Dr. Rachel.com 
Bioenergy Medical Center 
The Autism Center Austin 
Vaxxed II, The People’s Truth
Millions Against Medical Mandates
Centers for Advanced Medicine
Wellness Forum Health
Tenpenny Integrative Medical Center
V is for Vaccine
Immunity Education Group
Age of Autism
The Autism Trust U.S.A.
Plague of Corruption Book
Tommey Burrowes Productions LLP
Vaccine Choice Canada
Georgia Coalition For Vaccine Choice
Tennessee Coalition for Vaccine Choice

Countries in Unity:

United States
Canada
Japan
Germany
Brazil
France
Norway
Belarus
Belgium
Italy
Scotland
Mexico
New Zealand
Northern Ireland
Australia
Chile
Spain
Denmark
Nigeria
England
Cyprus
Israel

Script: United, We Say NO!

We stand together representing MILLIONS who proclaim the right to health freedom for our ourselves and our families.

In recent months, people around the world have suffered death, illness, shutdowns, quarantines, school closings, food shortages and other restrictions because of COVID.

And now we face a new threat – the threat of being bullied into vaccination.

Some are predicting we won’t get our lives back ‘til we get vaccinated. Some are saying that every person on the planet has to be vaccinated and tracked to “get back to normal.”

Now is this based on sound science?

Wasn’t the US founded on liberty? Who are these people anyways?

We are scientists, physicians, nurses, lawyers, religious leaders, parents, journalists and more. We are freedom-loving individuals who will never allow a liability-free, poorly-tested product to be injected into ourselves or our children.

We say “No!” Mandating an invasive medical procedure violates our most fundamental rights. All medical procedures, including vaccines, carry risks; they must be voluntary.

And vaccine injuries aren’t rare – they’re approximately 1 in every 40 doses, according to a  U.S. Agency for Health Research Quality 2010 study.

Being pressured to vaccinate — to stay in school, keep a job, get welfare benefits, or get on a plane – violates rights to personal autonomy, informed consent, parental rights, religious freedom, medical freedom, equal protection and due process.

What will you do when someone shows up at your door to vaccinate you or your children? We say “No!”. Will you consent — or refuse? If your employer, school or government can bully you into vaccinating, what’s next? More forced medicine? More forced tracking? All for the greater good??

We stand for your rights — and ours – including your right to consent. But know this:

  • No federally-recommended vaccine has ever been tested against a real placebo. Vaccines are tested against other vaccines or vaccine ingredients, masking harm. And the government has never tested the entire childhood schedule in vaccinated vs. unvaccinated children.
  • Vaccines are typically tested for days or weeks, not years, like drugs.
  • Government agencies charged with vaccine safety are, in essence, vaccine companies, owning patents and earning royalties. They are sock puppets of industry.
  • Mainstream media heavily censors information critical of vaccines. The vaccine companies spend billions every year in advertising revenue to the big media companies in our country, and they’re not only buying ad space, they are dictating content.
  • It’s important to know you can’t sue a vaccine manufacturer for a vaccine injury or death. Instead, you have to go through a government claims program where most people lose. Vaccine makers get all the profits, but the injured get all the losses — physical, mental, emotional and financial.
  • COVID-19 vaccines have received billions in government subsidy and private money. These vaccines have become “too big to fail,” even though the clinical trials have been disasters.

So, please: 

Be courageous!

Stand up for YOUR right to consent or refuse. 

Protect your individual and medical freedom rights!

You decide – not the government – what substances can be injected into your children’s bodies and your own.

Our health, our freedom and our future depend on what we do NOW! 

So say no, and stand firm.

Join the Movement!

Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is planning many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.

Bradykinin Hypothesis Explains COVID-19 Complexities


Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2020/09/14/bradykinin-hypothesis.aspx
Analysis by Dr. Joseph Mercola    Fact Checked    September 14, 2020

STORY AT-A-GLANCE

  • Genetic analysis using the Oak Ridge National Lab supercomputer has revealed an interesting new hypothesis — the bradykinin hypothesis — that helps explain the disease progression of COVID-19
  • The bradykinin hypothesis also strengthens the hypothesis that vitamin D plays a really important role in the disease
  • SARS-CoV-2 not only infects cells that naturally have high numbers of ACE2 receptors but also tricks your body into upregulating ACE2 receptors in places where they’re usually expressed at lower levels, such as your lungs
  • SARS-CoV-2 also downregulates your body’s ability to degrade or break down bradykinin, a chemical that helps regulate your blood pressure and is controlled by your renin-angiotensin system
  • The end result is a bradykinin storm, which appears to be the primary cause behind many of COVID-19’s lethal effects, even more so than the cytokine storms associated with the disease
  • The virus also increases production of hyaluronic acid (HLA) in your lungs. HLA has the ability to absorb more than 1,000 times its own weight in fluid, and when it combines with the built-up fluid in the lungs, it forms a thick hydrogel that makes breathing very difficult

Genetic analysis using the Oak Ridge National Lab supercomputer called the Summit has revealed an interesting new hypothesis that helps explain the disease progression of COVID-19. A September 1, 2020, Medium article1 by Thomas Smith reviewed the findings of what is now referred to as the bradykinin hypothesis.

As reported by Smith, the computer crunched data on more than 40,000 genes obtained from 17,000 genetic samples.

“Summit is the second-fastest computer in the world, but the process — which involved analyzing 2.5 billion genetic combinations — still took more than a week. When Summit was done, researchers analyzed the results. It was, in the words of Dr. Daniel Jacobson, lead researcher and chief scientist for computational systems biology at Oak Ridge, a ‘eureka moment.’”

The Bradykinin Hypothesis

Bradykinin is a chemical that helps regulate your blood pressure and is controlled by your renin-angiotensin system (RAS). As explained in the Academic Press’ book on vitamin D (which has a significant impact on the RAS):2

“The renin-angiotensin system (RAS) is a central regulator of renal and cardiovascular functions. Over-activation of the RAS leads to renal and cardiovascular disorders, such as hypertension and chronic kidney disease, the major risk factors for stroke, myocardial infarction, congestive heart failure, progressive atherosclerosis, and renal failure.”

The bradykinin hypothesis provides a model that helps explain some of the more unusual symptoms of COVID-19, including its bizarre effects on the cardiovascular system. It also strengthens the hypothesis that vitamin D plays a really important role in the disease.

The findings3 were published in the journal eLife July 7, 2020. Based on this new hypothesis, the researchers also suggest more than 10 potential treatments, most of which are readily available drugs already approved by the U.S. Food and Drug Administration. I’ll review those later on.

As detailed in previous articles, your ACE2 receptors are the primary gateways of the virus, as the virus’ spike protein binds to the ACE2 receptor. As explained by Smith:4

“… COVID-19 infection generally begins when the virus enters the body through ACE2 receptors in the nose … The virus then proceeds through the body, entering cells in other places where ACE2 is also present: the intestines, kidneys, and heart. This likely accounts for at least some of the disease’s cardiac and GI symptoms.

But once Covid-19 has established itself in the body, things start to get really interesting … The data Summit analyzed shows that COVID-19 isn’t content to simply infect cells that already express lots of ACE2 receptors. Instead, it actively hijacks the body’s own systems, tricking it into upregulating ACE2 receptors in places where they’re usually expressed at low or medium levels, including the lungs.

In this sense, COVID-19 is like a burglar who slips in your unlocked second-floor window and starts to ransack your house. Once inside, though, they don’t just take your stuff — they also throw open all your doors and windows so their accomplices can rush in and help pillage more efficiently.”

Click here to read more

Bradykinin Storm Likely Responsible for Lethal Effects

In addition to upregulating ACE2 receptors throughout your body, the SARS-CoV-2 virus also downregulates your body’s ability to degrade or break down bradykinin.

The end result is a bradykinin storm, and according to the researchers, this appears to be an important factor in many of COVID-19’s lethal effects, even more so than the cytokine storms associated with the disease. As bradykinin accumulates, the more serious COVID-19 symptoms appear.

Mounting clinical data suggest COVID-19 is actually primarily a vascular disease rather than a respiratory one, and runaway bradykinin buildup can help explain this.

How SARS-CoV-2 Attacks the Lungs

That said, COVID-19 certainly has a respiratory component, and it appears the virus attacks the lungs in more ways than one. For starters, bradykinin increases vascular permeability, essentially causing your blood vessels to leak fluid. In the lungs, this leads to fluid buildup that can trigger inflammation when immune cells also leak out into the lungs.

But the Summit data also show the virus uses yet another pathway, which raises production of hyaluronic acid (HLA) in your lungs. HLA has the ability to absorb more than 1,000 times its own weight in fluid, and when it combines with the built-up fluid in the lungs, the effect is devastating, as it ends up forming a thick hydrogel that makes breathing near-impossible.

When this happens — in severe cases — even mechanical ventilation becomes ineffective, as the alveoli in the lungs are simply too clogged with this gel-like substance that prevents oxygen uptake.

Note that the HLA produced in your lungs does not mean that using supplemental HLA is a bad strategy. It is only when HLA is produced locally in high concentrations in pathologic conditions like COVID-19 that it becomes problematic. Otherwise it has important physiologic benefits.

How SARS-CoV-2 Attacks Your Heart and Brain

SARS-CoV-2 can also affect heart function, causing arrhythmias and low blood pressure. About 1 in 5 COVID-19 patients requiring hospitalizations have experienced damage to their heart. Your heart has ACE2 receptors, so SARS-CoV-2 has the ability to infect your heart directly. Arrhythmias and low blood pressure can also be the result of a bradykinin storm.

In some cases, COVID-19 has also been known to trigger neurological symptoms such as dizziness, seizures, delirium and stroke, and this too can be explained by bradykinin buildup.

At high levels, bradykinin can lead to a breakdown of your blood-brain barrier, thereby allowing harmful compounds to flood your brain. Bradykinin itself also causes blood vessel leakage. Together, these effects can trigger inflammation, brain damage and a variety of neurological symptoms.

SARS-CoV-2 Mimics ACE Inhibiting Drugs

Interestingly, as reported by Smith:5

“Increased bradykinin levels could also account for other common COVID-19 symptoms. ACE inhibitors — a class of drugs used to treat high blood pressure — have a similar effect on the RAS system as COVID-19, increasing bradykinin levels.

In fact, Jacobson and his team note in their paper that ‘the virus … acts pharmacologically as an ACE inhibitor’ — almost directly mirroring the actions of these drugs.

By acting like a natural ACE inhibitor, COVID-19 may be causing the same effects that hypertensive patients sometimes get when they take blood pressure-lowering drugs. ACE inhibitors are known to cause a dry cough and fatigue, two textbook symptoms of COVID-19.

And they can potentially increase blood potassium levels, which has also been observed in COVID-19 patients. The similarities between ACE inhibitor side effects and COVID-19 symptoms strengthen the bradykinin hypothesis, the researchers say.”

Another side effect associated with ACE inhibiting drugs is the loss of smell and taste. This is also an early sign associated with SARS-CoV-2 infection, and it’s a primary symptom of zinc deficiency too.

Zinc, as explained in “Swiss Protocol for COVID — Quercetin and Zinc,” plays a vital role in immunity as well as in blood clotting, cell division, thyroid health, smell and taste, vision and wound healing, and can effectively inhibit viral replication.

Your body does not store zinc, and it’s poorly absorbed, which appears to be why the combination of zinc and zinc ionophores such as quercetin and hydroxychloroquine are so effective when taken at first symptoms.

Bradykinin Hypothesis Explains Other COVID-19 Symptoms Too

The bradykinin storm also helps explain other odd COVID-19 symptoms such as “COVID toes,” a condition in which your toes become swollen and bruised. This may be due to leaky vasculature in your toes.

As explained by Smith, it can also shed helpful light on the gender differences seen in COVID-19. Women tend to have a lower mortality rate than men, and this may be due to the fact that women have twice the level of certain proteins involved in the RAS system.

bradykinin storm
Image source: Daniel Jacobson et al. via eLife Sciences

Potential Treatments

The good news is that if bradykinin storms are to blame, there are a number of already existing drugs that can help prevent bradykinin storms, either reducing bradykinin or blocking its receptors. As noted in the study:6

“Several interventional points (most of them already FDA-approved pharmaceuticals) could be explored with the goal of increasing ACE, decreasing BK [bradykinin], or blocking BK2 receptors.

Icatibant is a BKB2R antagonist whereas Ecallantide acts to inhibit KLKB1, reducing levels of BK production. Androgens (danazol and stanasolol) increase SERPING1, although the side effects likely make these undesirable, but recombinant forms of SERPING1 could be administered to reduce BK levels.

It should be noted that any intervention may need to be timed correctly given that REN levels rise on a diurnal cycle, peaking at 4AM which corresponds with the commonly reported worsening of COVID-19 symptoms at night …

4-methylumbelliferone (Hymecromone) is a potent inhibitor of HAS1, HAS2, and HAS3 gene expression and results in the suppression of the production of hyaluronan in an ARDS model.

Hymecromone (4-methylumbelliferone) is approved for use in Asia and Europe for the treatment of biliary spasm. However, it can cause diarrhea with subsequent hypokalemia, so considerable caution should be used if this were to be tried with COVID-19 patients … Timbetasin may reduce COVID-19 related coagulopathies by increasing fibrinolysis.”

However, please understand that taking these drugs is absolutely not my recommendation. These are simply the conventional strategies that can be used if this hypothesis is correct.

Why on earth would we use dangerous drugs like these for a disease that they have not been tested on when we have so many other safe, inexpensive and highly effective interventions for COVID-19? Strategies like nebulized peroxide, ozone, molecular hydrogen, exogenous ketones, and quercetin with zinc.

Evidence for Vitamin D Strengthens

The researchers also highlight the usefulness of vitamin D, noting that “Another approach would be the modulation of REN levels via Vitamin D supplementation …” Vitamin D is involved in the RAS system,7,8,9 and can reduce a compound called renin (REN), thereby preventing a deadly bradykinin storm. Renin is an endopeptidase, the function of which is to generate angiotensin 1 from angiotensinogen in your plasma.

If you are vitamin D deficient, your renin expression is stimulated, and based on the latest data, that may render you more prone to bradykinin storm.

Several investigations have highlighted the apparent influence of vitamin D in COVID-19 incidence, severity and mortality, and its effects on RAS further strengthens the idea that vitamin D may be a crucial component in your COVID-19 defense arsenal.

As explained in the 2004 paper,10 “Vitamin D: A Negative Endocrine Regulator of the Renin-Angiotensin System and Blood Pressure,” when the RAS system is inappropriately activated, high blood pressure can result.

One factor that influences your RAS is your vitamin D level, as it suppresses renin biosynthesis. If you are vitamin D deficient, your renin expression is stimulated, and based on the latest data, that may render you more prone to bradykinin storm.

The Evidence for Vitamin D

In a November 1, 2020 commentary11 in the journal Metabolism Clinical and Experimental, JoAnn Manson and Shari Bassuk call for the elimination of vitamin D deficiency to effectively squelch the COVID-19 pandemic, noting that 23.3% of the total U.S. population have insufficient or deficient vitamin D levels, with people of color having disproportionately lower levels than non-Hispanic whites.

They list several types of studies showing vitamin D deficiency is “an important modifiable risk factor for COVID-19,” including:12

Laboratory studies that demonstrate how vitamin D helps regulate immune function and the RAS, and modulate inflammatory responses to infection.

Ecologic studies showing populations with lower vitamin D levels or lower UVB radiation exposure have higher COVID-19 mortality,13,14,15 and the fact that people identified as being at greatest risk for COVID-19 hospitalization and death (people of color, the elderly, nursing home residents and those with comorbidities such as obesity, vascular conditions and chronic kidney disease) also have a higher risk of vitamin D deficiency.

A pilot randomized clinical study16,17 published online August 29, 2020, found hospitalized COVID-19 patients in Spain who were given supplemental vitamin D (calcifediol) in addition to standard of care — which included the use of hydroxychloroquine and azithromycin — had significantly lower intensive care unit admissions.

Patients in the vitamin D arm received 532 micrograms of calcifediol on the day of admission (equivalent to 106,400 IUs of vitamin D18) followed by 266 mcg on Days 3 and 7 (equivalent to 53,200 IUs19). After that, they received 266 mcg once a week until discharge, ICU admission or death.

Of those receiving calcifediol, only 2% required ICU admission, compared to 50% of those who did not get calcifediol. None of those given vitamin D supplementation died, and all were discharged without complications.

Observational studies showing low vitamin D levels are associated with a greater risk of testing positive for SARS-CoV-2 and contracting acute respiratory infections.

Most recently, a September 3, 2020 JAMA study20 reported that people who tested positive for SARS-CoV-2 were 1.77 times more likely to be deficient in vitamin D than those who tested negative for the virus.

Randomized clinical trials showing vitamin D inhibits respiratory tract infections, especially in those with lower vitamin D levels at baseline.

REALLY IMPORTANT: Optimize Your Vitamin D Level Now

For years, I’ve stressed the importance of optimizing your vitamin D level, especially in anticipation of flu season, and it seems clear it can go a long way toward protecting yourself against COVID-19 as well.

Aside from what’s already been mentioned, vitamin D also helps Type II cells in your lungs produce surfactant that aids in fluid clearance. When you’re vitamin D deficient, your entire RAS is deranged or dysfunctional, thereby raising your risk of both bradykinin storm and cytokine storm.

In closing, experts have been warning that SARS-CoV-2 may reemerge in the fall when temperatures and humidity levels drop, thereby increasing the virus’ transmissibility.

Now is the time to check your vitamin D level and start taking action to raise it if you’re below 60 ng/mL. An easy and cost-effective way of measuring your vitamin D level is to order GrassrootsHealth’s vitamin D testing kit and learn more about vitamin D and its impact on your health.

Knowledge is empowerment, and that is particularly true during this pandemic. To learn more about the influence of vitamin D on your health in general and COVID-19 in particular, see my vitamin D report.

Gates-funded polio vaccine causing polioviruses, WHO admits

Reproduced from original article:
www.naturalhealth365.com/polio-bill-gates-africa-3551.html
|  September 11, 2020

polio-vaccine(NaturalHealth365) When mainstream media has its way, any criticism of billionaire computer geek – turned so-called global health expert – Bill Gates is quickly quashed with accusations of “conspiratorial arrogance.”  But when even the World Health Organization (WHO) is forced to acknowledge that a polio vaccine funded by Gates is responsible for a polio outbreak, it’s nearly impossible not to feel alarmed by the billionaire’s huge presence in the worldwide medical sphere.

The outbreak in Africa is one of at least two dozen confirmed episodes of vaccine-derived polio outbreaks throughout the world over the past five years, affecting countries ranging from the Phillippines to Ukraine … and despite this news, we’re supposed to depend on a Bill Gates-backed COVID vaccine (rushed to market) – which “hopefully” restores life as usual after the coronavirus pandemic?!

Over a dozen cases: Polio outbreak in Africa linked to polio vaccine funded by Bill Gates

On September 1, 2020, the WHO announced on their website that just one month prior, the Federal Ministry of Health in Sudan notified the troubled organization of an emerging “vaccine-derived” polio outbreak, caused by what’s known as poliovirus type 2, or cVDPV2.  Sudanese officials so far have identified two young children suffering the effects of the vaccine.

“The first case,” reports the WHO, was a four-year-old child who experienced “onset of [acute flaccid paralysis] on 7 March 2020 … in South Darfur,” located in Western Sudan. The next child to become paralyzed by a vaccine was a three-year-old from “Shari city of AI Gedarif locality in Gedarif state in the east, close to the border with Eritrea and Ethiopia.”

“Both children,” the WHO admits, “received their last bOPV ( type 1 & 3) dose in 2019.”

In just the month of August alone, a total of 13 cases of cVDPV2 have been reported all over Africa, including the areas of the Red Sea, West Darfur, East Darfur, White Nile, River Nile, and Gezira. These cases are genetically linked to another vaccine-derived outbreak detected back in October 2019 and currently circulating in Chad and Cameroon.

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Myth buster: Far from eradicated, sickness is raging in certain parts of the world directly as a result of Gates-funded vaccines, experts say

Vaccine manufacturers and their backers – including the Bill and Melinda Gates Foundation – long tout the importance of vaccines to prevent communicable diseases and save lives around the world, especially in more vulnerable populations such as Sub-Saharan Africa.

And yet it’s clear from recent reports that this isn’t always the case.  To be blunt, many people greatly doubt the “good intentions” of Bill Gates and see him merely as a profiteer – making billions of dollars due to his vaccination agendas.

The problem is so concerning that a virologist from the U.S. Centers for Disease Control and Prevention, Mark Pallansch, admitted in a Science magazine interview from last year that because of widespread use of newer, more powerful polio vaccines, “[w]e have now created more new emergences of the virus than we have stopped.”

According to a recent report from Nature, cases of wild polio in Africa are virtually non-existent since 2016, but over 400 cases of polio caused by the vaccine have been documented in 20 countries around the world in just the last year (August 2019 to August 2020).

That’s right!  We have it from the highest authority that vaccines are spreading virulent strains of a potentially deadly virus.  We’ve had official reports of this for years, in fact. In light of this frightening reality, we have to wonder:

Will officials really keep denying the serious risks of forcing mass vaccination of a hastily-made COVID vaccine onto the unsuspecting (and perhaps all-too-trusting) public?

Sources for this article include:

WHO.int
Nature.com
Childrenshealthdefense.org
Sciencemag.org
WHO.int

Will New COVID Vaccine Make You Transhuman?


Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2020/09/12/coronavirus-vaccine-transhumanism.aspx
Analysis by Dr. Joseph Mercola    Fact Checked    September 12, 2020

STORY AT-A-GLANCE

  • The goal of the transhumanist movement, or “Human 2.0,” is to transcend biology into technology, to meld human biology with technology and artificial intelligence
  • Right now, today, we may be standing at the literal crossroads of transhumanism, thanks to the fast approaching release of one or more mRNA COVID-19 vaccines
  • COVID-19 mRNA vaccines are designed to instruct your cells to make the SARS-CoV-2 spike protein. It does this through a process called transfection, which is also used to create genetically engineered organisms
  • Transfection can have either temporary or permanent effects on the genome, and it is unclear how the COVID-19 vaccines may affect the human genome long-term
  • In 2019, researchers discovered the 2009 pandemic swine flu vaccine Pandemrix caused narcolepsy by affecting a non-coding RNA gene that regulates the production of glial cell line-derived neurotrophic factor, a protein that plays an important role in neuronal survival. If a conventional vaccine can have genetic effects, the risk of mRNA vaccines having genetic effects is bound to be even greater

Two years ago, in October 2018, Forbes contributor Neil Sahota, a United Nations artificial intelligence adviser and UC Irvine professor, warned that transhumanism is fast approaching — likely faster than you think.1

“In the past few years, there has been considerable discussion around the idea we are slowly merging with our technology, that we are becoming transhuman, with updated abilities, including enhanced intelligence, strength, and awareness,” Sahota writes.

The goal of the transhumanist movement, or “Human 2.0,” is to transcend biology into technology. Or, as Dr. Carrie Madej explains in the video above, to meld human biology with technology and artificial intelligence.

Two visible proponents of transhumanism are Ray Kurzweil (director of engineering at Google since 2012) and Elon Musk (founder of SpaceX, Tesla and Neuralink).

Standing at the Crossroads of Transhumanism

According to Madej, right now, today, we may be standing at the literal crossroads of transhumanism, thanks to the fast approaching release of one or more mRNA COVID-19 vaccines.

Many of the COVID-19 vaccines currently being fast-tracked are not conventional vaccines. Their design is aimed at manipulating your very biology, and therefore have the potential to alter the biology of the entire human race.

Conventional vaccines train your body to recognize and respond to the proteins of a particular virus by injecting a small amount of the actual viral protein into your body, thereby triggering an immune response and the development of antibodies.

This is not what happens with an mRNA vaccine. The theory behind these vaccines is that when you inject the mRNA into your cells, it will stimulate your cells to manufacture their own viral protein.2 The mRNA COVID-19 vaccine will be the first of its kind. No mRNA vaccine has ever been licensed before. And, to add insult to injury, they’re forgoing all animal safety testing.

Madej reviews some of the background of certain individuals participating in the race for a COVID-19 vaccine, which include Moderna co-founder Derrick Rossi, a Harvard researcher who successfully reprogrammed stem cells using modified RNA, thus changing the function of the stem cells. Moderna was founded on this concept of being able to modify human biological function through genetic engineering, Madej says.

Side Effects Should Be Expected

As mentioned, the mRNA vaccines are designed to instruct your cells to make the SARS-CoV-2 spike protein, the glycoprotein that attaches to the ACE2 receptor of the cell. This is the first stage of the two-stage process viruses use to gain entry into cells.

The idea is that by creating the SARS-CoV-2 spike protein, your immune system will mount a response to it and begin producing antibodies to the virus. However, as reported by The Vaccine Reaction, researchers have pointed out potential weaknesses:3

According to researchers at University of Pennsylvania and Duke University, mRNA vaccines have potential safety issues, including local and systemic inflammation and stimulation of auto-reactive antibodies and autoimmunity, as well as development of edema (swelling) and blood clots.4

Systemic inflammation, auto-reactive antibodies and autoimmune problems are not insignificant concerns. In fact, these are in large part why previous attempts to create a coronavirus vaccine have ALL failed.

Over the past 20 years, coronavirus vaccine research has been plagued by one consistent adverse outcome in particular, namely paradoxical immune enhancement. This is caused by the fact that coronaviruses produce two different types of antibodies — neutralizing antibodies5 that fight the infection, and binding antibodies6 (also known as nonneutralizing antibodies) that cannot prevent viral infection.

Incapable of preventing viral infection, binding antibodies can instead trigger paradoxical immune enhancement. What that means is that it looks good until you get the disease, and then it makes the disease far worse than it would have been otherwise. As detailed in my interview with Robert F. Kennedy Jr., in one coronavirus vaccine trial using ferrets, all the vaccinated animals died when exposed to the actual virus.

According to Madej, animal studies have also found the type of mRNA technology introduced with this vaccine can increase the risk of cancer and mutagenesis (gene mutations).

Click here to read more

What You Need to Know About the Delivery System

Madej goes on to discuss how this mRNA vaccine is going to be administered. Rather than a conventional injection, the vaccine will be administered using a microneedle platform. Not only can it be mass produced quickly, but it can also be administered by anyone. It’s as simple at attaching an adhesive bandage to your arm.

The adhesive side of the bandage has rows of tiny microneedles and a hydrogel base that contains luciferase enzyme and the vaccine itself. Because of their tiny size, the microneedles are said to be nearly painless when pressed into the skin.

The idea is that the microneedles will puncture the skin, delivering the modified synthetic RNA into the nucleus of your cells. RNA is essentially coding material that your body uses. In this case, as mentioned, the instructions are to produce the SARS-CoV-2 viral protein.

The problem with all of this, Madej notes, is that they’re using a process called transfection — a process used to create genetically modified organisms. She points out that research has confirmed GMO foods are not as healthy as conventional unmodified foods. The question is, might we also become less healthy?

“Vaccine manufacturers have stated that this will not alter our DNA, our genome,” Madej says. “I say that is not true. Because if we use this process to make a genetically modified organism, why would it not do the same thing to a human? I don’t know why they’re saying that.

If you look at the definition of transfection, it will tell you that it can be a temporary change in the cell. And I think that is what the vaccine manufacturers are banking on.

Or, it’s a possibility for it to become stable, to be taken up into the genome, and to be so stable that it will start replicating when the genome replicates. Meaning it is now a permanent part of your genome. That’s a chance that we’re taking. It could be temporary, or it could be permanent.”

Patentable DNA, Luciferase and Nanotechnology

Naturally, we won’t find out the truth about whether the vaccine causes a temporary or permanent change for many years after the experimental vaccine is introduced, and that’s an important piece of information.

Why? Because synthetic genes can be patented. So, if inserting a synthetic RNA ends up creating permanent changes in the genome, humans will contain patentable genes. What will that mean for us, seeing how patents have owners, and owners have patent rights?

Another part of the delivery system that raises its own set of questions is the use of the enzyme luciferase, which has bioluminescent qualities. While invisible under normal conditions, using a cellphone app or special device, you will be able to see a glowing vaccination mark.

As described in the journal RSC Advances7 in 2015, luciferase gene-loaded quantum dots “can efficiently deliver genes into cells.” The abstract discusses their use as “self-illuminating probes for hepatoma imaging,” but the fact that quantum dots can deliver genetic material is interesting in itself.

The hydrogel, meanwhile, is a DARPA invention that involves nanotechnology and nanobots. This “bioelectronic interface” is part of how the vaccination mark will be able to connect to your smartphone, Madej says, providing information about blood sugar, heart rate and any number of other biological data.

“It has the potential to see almost anything that goes on in your body,” Madej says. This will have immediate ramifications for our privacy, yet no one has yet addressed where this information will be going. Who will collect and have access to all this data? Who will be responsible for protecting it? How will it be used?

Also, if your cellphone can receive information from your body, what information can your body receive from it, or other sources? Could transmissions affect our mood? Our behavior? Our physical function? Our thoughts or memories?

Stepping Into Transhumanist Territory

In his Forbes article,8 Sahota quotes Kurzweil’s book “The Singularity Is Near: When Humans Transcend Biology,” in which Kurzweil states:

“The Singularity will represent the culmination of the merger of our biological thinking and existence with our technology, resulting in a world that is still human but that transcends our biological roots.”

If Madej turns out to be correct, and the mRNA vaccine ushers in the ability to alter not only our genes but also opens the door for nanotechnology-driven interfacing between our bodies and programmable technology, aren’t we in fact stepping over the line into transhuman territory?

The Truthstream Media video above discusses the larger issues of transhumanism and the race to merge man with machine and artificial intelligence. There are even ongoing attempts to upload the human mind into the cloud, ultimately creating a form of “digital hive mind” where everyone communicates via “Wi-Fi telepathy.” This, despite the fact we still do not fully understand what “the mind” actually is, or where it’s located.

Neuralink — A Psychiatric Disaster in the Making?

Another transhumanist that has recently brought us to a brand-new precipice is Elon Musk, with his latest venture, Neuralink, described in the video presentation given in late August, above. Neuralink is a transcranial implant that uses direct current stimulation. For now, the device is aimed at helping people with brain or spinal injuries.

Ultimately, the goal is to merge the human brain with computers. I have strong reservations about this. There’s tremendous room for unintended psychological and psychiatric consequences. In an interview that I did with psychiatrist Dr. Peter Breggin that has not yet been published, he discussed his concerns with this technology, saying:

“What’s interesting to me is that while Musk is so brilliant, he’s stupid about the brain. That’s probably because the neurosurgeons and psychiatrists he consults are stupid about the brain. I mean they’re just stupid.

He wants to put in multiple threadlike electrodes into the brain, into webs of neurons, and put in low voltage stimulation. This is insane. The brain can’t tolerate this. He hopes to [be able to] communicate but there’s not going to be any communication.

The brain isn’t going to talk to these electrodes. That’s not how the brain works. The brain talks to itself. It’s not going to talk to Elon Musk [or anyone else] and he’s going to disrupt the brain talking to itself. It’s a terrible thing to do.

I wish somebody who knows Elon Musk would say, ‘You ought to talk to Peter Breggin. He says your consultants are stupid.’ He’s already planning to try to get FDA approval for some neurological disorders and that’ll be the beginning of the onslaught.”

Is Transhumanism Inevitable?

Getting back to the mRNA vaccines, time will tell just how hazardous they end up being. Clearly, if the changes end up being permanent, the chance of long-term side effects is much greater than if they end up being temporary.

In a worst-case scenario, whatever changes occur could even be generational. The problem is these issues won’t be readily apparent any time soon. In my view, this vaccine could easily turn into a global catastrophe the likes of which we’ve never experienced before.

We really should not be quick to dismiss the idea that these vaccines may cause permanent genetic changes, because we now have proof that even conventional vaccines have the ability to do that, and they don’t involve the insertion of synthetic RNA.

Fast-Tracked Swine Flu Vaccine Caused Genetic Alterations

After the H1N1 swine flu of 2009, the ASO3-adjuvanted swine flu vaccine Pandemrix (a fast-tracked vaccine used in Europe but not in the U.S. during 2009-2010) was causally linked9 to childhood narcolepsy, which abruptly skyrocketed in several countries.10,11

Children and teens in Finland,12 the U.K.13 and Sweden14 were among the hardest hit. Further analyses discerned a rise in narcolepsy among adults who received the vaccine as well, although the link wasn’t as obvious as that in children and adolescents.15

A 2019 study16 reported finding a “novel association between Pandemrix-associated narcolepsy and the non-coding RNA gene GDNF-AS1” — a gene thought to regulate the production of glial cell line-derived neurotrophic factor or GDNF, a protein that plays an important role in neuronal survival.

They also confirmed a strong association between vaccine-induced narcolepsy and a certain haplotype, suggesting “variation in genes related to immunity and neuronal survival may interact to increase the susceptibility to Pandemrix-induced narcolepsy in certain individuals.”

In addition to that, there’s the research17 showing that the H1N1 swine flu vaccine was one of five inactivated vaccines that increased overall mortality, especially among girls. A swine flu article I wrote 11 years ago, in 2009, turned out to have a rather prophetic warning at the end:

The swine flu vaccine has not been tested for safety or efficacy, but we DO know it will contain harmful additives. The choice, to me, is obvious. And in the future, anytime a new ‘pandemic’ appears and officials urge you to rush out and get a shot, please remember this article and ask yourself if it’s really you who stands to benefit from their advice.”

The Swine Flu Fraud of 1976

We can also learn from the swine flu fiasco of 1976, detailed in this 1979 “60 Minutes” episode. Fearing a repeat of the 1918 Spanish flu pandemic, “the government propaganda machine cranked into action,” “60 Minutes” says, telling all Americans to get vaccinated.

According to “60 Minutes,” 46 million Americans were vaccinated against the swine flu at that time. Over the next few years, thousands of Americans filed vaccine damage claims with the federal government.18 As reported by Smithsonian Magazine in 2017:19

“In the spring of 1976, it looked like that year’s flu was the real thing. Spoiler alert: it wasn’t, and rushed response led to a medical debacle that hasn’t gone away.

‘Some of the American public’s hesitance to embrace vaccines — the flu vaccine in particular — can be attributed to the long-lasting effects of a failed 1976 campaign to mass-vaccinate the public against a strain of the swine flu virus,’ writes Rebecca Kreston for Discover.

‘This government-led campaign was widely viewed as a debacle and put an irreparable dent in future public health initiative, as well as negatively influenced the public’s perception of both the flu and the flu shot in this country.’”

A 1981 report by the U.S. General Accounting Office to Sen. John Durkin, D-N.H., reads, in part:20

“Before the swine flu program there were comparatively few vaccine-related claims made against the Government. Since 1963, Public Health Service records showed that only 27 non-swine flu claims were filed.

However, as of December 31, 1979, we found that 3,839 claims and 988 lawsuits had been filed against the Government alleging injury, death, or other damage resulting from the 45 million swine flu immunizations given under the program.

A Justice official told us that as of October 2, 1980, 3,965 claims and 1,384 lawsuits had been filed. Of the 3,965 claims filed, the Justice official said 316 claims had been settled for about $12.3 million …”

The devastating side effects of the Pandemrix vaccine should be instructive. No one anticipated a flu vaccine to have genetic consequences, yet it did. Now they’re proposing injecting mRNA to make every single cell in your body produce the SARS-CoV-2 spike protein.

It seems outright foolish not to assume there will be significant consequences. Perhaps even transhumanistic ones? The 1976 swine flu hoax is equally instructive, in that it demonstrates the long history of mass vaccination campaigns causing far more harm than good.