Health & Fitness

DarkHorse host Bret Weinstein, Ph.D., has conducted a couple of long and really valuable interviews in recent weeks. One was with a lung and ICU specialist, Dr. Pierre Kory, who is also the president and chief medical officer¹ of the Frontline COVID-19 Critical Care Alliance (FLCCC). The FLCCC has published three different COVID-19 protocols, all of which include the use of ivermectin:

• I-MASK+² — a prevention and early at-home treatment protocol
• I-MATH+³ — an in-hospital treatment protocol. The clinical and scientific rationale for this protocol has been peer-reviewed and was published in the Journal of Intensive Care Medicine⁴ in mid-December 2020
• I-RECOVER⁵ — a long-term management protocol for long-haul syndrome

In another episode, Weinstein interviewed Dr. Robert Malone, the inventor of the mRNA and DNA vaccine technology.⁶ In both instances, YouTube deleted the videos. Why? Because they discussed science showing ivermectin works against COVID-19 and the hazards of COVID gene therapies. Never mind the fact that Kory and Malone are the widely recognized leading experts in their fields.

In the wake of this targeted takedown, podcast host Joe Rogan invited Weinstein and Kory in for an “emergency podcast” about the censorship of ivermectin. As noted by Weinstein in a June 23, 2021, tweet, “The censorship campaign obscuring Ivermectin (as prophylactic against SARS-CoV2 and as treatment for COVID-19) kills.”⁷

Indeed, we now know that early treatment is crucial to prevent complications, hospitalizations, death and/or long-haul syndrome, so censoring this information is inexcusable, and has without doubt resulted in needless deaths.

What Is Misinformation?

As Weinstein explains, there are several things in dire need of discussion. For starters, there’s the issue of YouTube’s community guidelines and posting rules, which are so vague that it’s impossible to determine beforehand if something is going to be deemed in violation.

Violations, in turn, threaten the ability of people like Weinstein to make a living. His entire family depends on the income generated through his YouTube channel. He now has two strikes against him, where YouTube claims he’s been posting “spam” and “medical misinformation.” One more, and the entire channel will be demonetized.

A central problem here is, who determines what misinformation is? YouTube has taken the stance that anything that goes against what the World Health Organization says is medical misinformation. However, the WHO doesn’t always agree with other public health agencies.

For example, the WHO does not recommend the drug remdesivir, but the U.S. Centers for Disease Control and Prevention does, and virtually all U.S. hospitals routinely use the drug on COVID-19 patients.

Another example where the WHO and the CDC are in disagreement is how the virus can be transmitted. While the CDC admits SARS-CoV-2 is an airborne virus that transmits through the air, the WHO does not list air as a form of transmission. So, is the CDC putting out medical misinformation?

Censorship Is a Disinformation Tool

As Weinstein rightly points out, if the WHO (or virtually every federal regulatory agency for that matter) has been captured and is being influenced by industry, in this case Big Pharma, and is itself putting out information that goes against medical science, then this is something that must be discussed and exposed. That is precisely what he did in the two episodes that YouTube wiped.

If an organization is putting out medical misinformation, and talking about this is censored, the end result is going to be devastating to public health. Overall, we’re in an untenable situation, Weinstein says, as people are losing their livelihoods simply for discussing the science and laying out the evidence. Licensed, practicing doctors are prevented from sharing practical knowledge that can save lives.

The fact that YouTube is making up the rules as they go is clear. One of Weinstein’s interviews was deemed to be “spam.” How can a discussion between highly respected and well-credentialed scientists and medical professionals be spam? YouTube obviously couldn’t determine what was incorrect about it so they simply made up an excuse to take the video down.

Or more likely, they knew exactly what they were doing and removed it because it countered what appears to be their primary agenda, which is to promote the COVID jab.

As noted in the featured interview, censorship is actually a form of disinformation, which is defined as “information given to hide the actual truth.” A perfect example of this is the suppression of the lab-leak theory. For a year and a half, no one was allowed to discuss the possibility that SARS-CoV-2 originated in a Wuhan lab. There’s no telling how many tens of thousands of people lost their social media accounts, including yours truly, because they violated this rule.

The lab-leak theory was “debunked,” according to all the industry-backed fact checkers. Now, all of a sudden, the evidence has somehow taken root and everyone is talking about it. Mainstream media pundits are squirming in their seats, trying to explain why they overlooked the obvious and roundly dismissed the evidence for so long. What was “misinformation” yesterday is now “fact.”

Who decided this? Big Tech censored verifiable facts for a year and a half, and there’s every reason to assume they censored it on behalf of someone. They grossly misinformed — nay, disinformed — the public, yet they’re not held accountable for any of it.

The Manufacturing of Medical and Scientific Consensus

As noted by Weinstein, the idea that medical and scientific consensus can be established seemingly from one day to another in the middle of a pandemic involving a novel virus is simply not believable. It cannot happen, because scientific and medical consensus arises over time, as experts challenge each other’s theories.

A hypothesis may sound good, but will break apart once another piece of evidence is added. So, it changes over time. What happened here, however, over the last year and a half, is that a consensus was declared early on, and subsequent evidence was simply discarded as misinformation.

The examples of this are numerous. Take vitamin D, for example. We’ve long known vitamin D influences your immune system. Yet the manufactured consensus declared vitamin D irrelevant in the case of COVID-19, and this stance remains to this day, even though dozens of studies have now demonstrated that vitamin D plays a crucial role in COVID-19 outcomes specifically.

The lab leak theory is another example. Manufactured consensus declared it bunk, and that was it. Face masks were declared effective without any evidence, and anyone pointing out the discrepancy between this recommendation and what the scientific literature was showing was simply declared to be violating some vaguely defined “community standards.”

Manufactured consensus declared hydroxychloroquine and ivermectin dangerous and/or useless, saying we can’t possibly risk using these drugs unless they’re proven safe and effective in large randomized controlled trials (RCTs). As noted by Weinstein, they willingly roll the dice when it comes to the novel COVID shots, yet apply ridiculously high standards of safety and effectiveness when it comes to off-patent drugs that have decades of safe use.

There’s something very unnatural and unscientific about all of this, and that raises serious questions about intent. What is the intent behind these manufactured consensuses that by any reasonable standard have been proven flawed or incorrect?

For all the talk about preventing dangerous misinformation being spread by the average person, governments, Big Pharma, Big Tech and nongovernmental organizations that have a great deal of influence over nations, have in fact engaged in the biggest disinformation campaign in human history. The question is why?

As noted by Kory, over time, he has developed a deep cynicism about many of the agencies and organizations that are supposed to protect public health, because their recommendations and conclusions do not comport with good science. And, if we trust them exclusively, we can get into real trouble.

The thing is, there must be a reason for why they don’t follow the science, and that, most likely, is because they’re beholden to financial interests. If the science doesn’t support those financial interests, it’s disregarded.

This is why, by and large, there’s a very clear dividing line between those who promote the ideas of the WHO, the CDC and the U.S. Food and Drug Administration, and those who don’t.

Those who disagree with the manufactured consensus are almost exclusively independent, meaning they’re not financially dependent on an organization, company or agency to which the facts are inconvenient.

“Heretics” also tend promote products that they cannot make a profit from, such as hydroxychloroquine and ivermectin, two drugs that have been used for so long they’re off-patent. Alternatively, they recommend natural products like vitamin D, which is virtually free, especially if you get it from optimal sun exposure.

Gold Standard Evidence Supports Ivermectin

As noted by Kory, while the WHO insists large RCTs must be completed before ivermectin (or hydroxychloroquine) can be recommended, RCTs actually are not the gold standard in terms of scientific evidence. Meta-analyses are.

The reason for this is because any given trial can be skewed by any number of protocol factors. When you do a meta-analysis of several trials, even if those trials are small, you have the best chance of detecting signals of danger or benefit because it corrects for flaws in the various protocols.

In the case of ivermectin, FLCCC recently conducted a meta-analysis⁸ of 24 RCTs, which clearly demonstrates that ivermectin produces “large statistically significant reductions in mortality, time to clinical recovery, and time to viral clearance.”

They also found that when used as a preventive, ivermectin “significantly reduced risks of contracting COVID-19.” In one study, of those given a dose of 0.4 mg per kilo on Day 1 and a second dose on Day 7, only 2% tested positive for SARS-CoV-2, compared to 10% of controls who did not get the drug.

In another, family members of patients who had tested positive were given two doses of 0.25 mg/kg, 72 hours apart. At follow up two weeks later, only 7.4% of the exposed family members who took ivermectin tested positive, compared to 58.4% of those who did not take ivermectin.

In a third, which unfortunately was unblended, the difference between the two groups was even greater. Only 6.7% of the ivermectin group tested positive compared to 73.3% of controls. Still, according to the FLCCC, “the difference between the two groups was so large and similar to the other prophylaxis trial results that confounders alone are unlikely to explain such a result.”

The FLCCC also points out that ivermectin distribution campaigns have resulted in “rapid population-wide decreases in morbidity and mortality,” which indicate that ivermectin is “effective in all phases of COVID-19.” For example, in Brazil, three regions distributed ivermectin to its residents, while at least six others did not. The difference in average weekly deaths is stark.

In Santa Catarina, average weekly deaths declined by 36% after two weeks of ivermectin distribution, whereas two neighboring regions in the South saw declines of just 3% and 5%. Amapa in the North saw a 75% decline, while the Amazonas had a 42% decline and Para saw an increase of 13%. Importantly, ivermectin’s effectiveness also appears largely unaffected by variants, meaning it has worked on any and all variants that have so far popped up around the world.

Kory also points out that once you can see from clinical evidence that something really is working, then conducting RCTs becomes unethical, as you know you’re condemning the control group to poor outcomes or death. This is, in fact, the same argument vaccine makers now use to justify the elimination of control groups by giving everyone the vaccine.

All of that said, RCT evidence for ivermectin will hopefully come from the British PRINCIPLE trial,⁹ which began June 23, 2021. Ivermectin will be evaluated as an outpatient treatment in this study, which will be the largest clinical trial to date.

How Ivermectin Works

While ivermectin is best known for its antiparasitic properties, it also has both antiviral and anti-inflammatory properties. With regard to how it can help against SARS-CoV-2 infection, studies¹⁰ have shown ivermectin lowers your viral load by inhibiting replication.

In “COVID-19: Antiparasitic Offers Treatment Hope,” I review data showing a single dose of ivermectin killed 99.8% of SARS-CoV-2 in 48 hours. A recent meta-analysis¹¹ by Dr. Tess Lawrie found the drug reduced COVID-19 infection by an average of 86% when used preventatively. 

An observational study¹² from Bangladesh, which looked at ivermectin as a preexposure prophylaxis for COVID-19 among health care workers, found only four of the 58 volunteers who took 12 mg of ivermectin once per month for four months developed mild COVID-19 symptoms between May and August 2020, compared to 44 of the 60 health care workers who had declined the medication.

Ivermectin has also been shown to speed recovery, in part by inhibiting inflammation through several pathways and protecting against organ damage. This, of course, also lowers your risk of hospitalization and death, which has been confirmed in several studies.

Meta-analyses have shown average reductions in mortality ranging from 75%¹³ to 83%^14,15 The drug has also been shown to prevent transmission of SARS-CoV-2 when taken before or after exposure. When you add all of these benefits together, it seems fairly clear that ivermectin use could vaporize this pandemic.

Where You Can Learn More

While ivermectin certainly appears to be a useful strategy, which is why I am covering it, it is not my primary recommendation. In terms of prevention, I believe your best bet is to optimize your vitamin D level, as your body needs vitamin D for a wide variety of functions, including a healthy immune response.

As for early treatment, I recommend nebulized hydrogen peroxide treatment,^16,17 which is inexpensive, highly effective and completely harmless when you’re using the low (0.04% to 0.1%) peroxide concentration recommended.

All of that said, ivermectin and several other remedies certainly have a place, and it’s good to know they exist and work well. On the whole, there’s really no reason to remain panicked about COVID-19. If you want to learn more about ivermectin, there are several places where you can do that, including the following:

Mark Your Calendars for VERY Important Interview!

Please be sure to mark your calendar so you don’t miss my groundbreaking interview with Dr. Vladimir Zelenko, July 4, 2021. We discuss the very distinct possibility that everyone who receives the COVID jab may die from complications in the next two to three years.

You should have plenty of time to view this vitally important exchange of information as it is the national Fourth of July holiday. We literally share life-changing information, so please be sure to read it and share with your friends.

This is largely because getting the jab now immediately places the injected individual in the very high risk of dying from COVID. Most have the false assurance that they are protected but, in reality, they are far more vulnerable and as a result will not take very aggressive proactive measures to avoid dying from pathogenic priming or paradoxical immune enhancement before it is too late.

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We’re seeing the rapid emergence of two sets of people — those who are vaccinated against COVID-19 and those who are not. A distinction need not be made, as whether or not to receive medical procedures is a personal choice that should remain private if you so choose.

But increasingly, people are being required to prove that they’re vaccinated in order to go about their daily lives, while those who are unvaccinated are losing privileges.

While many countries have suggested that the COVID-19 vaccine will not be mandated, by giving special privileges to the vaccinated, such as the ability to travel, attend social events or even enter a workplace, it essentially amounts to the same thing and insinuates a “cleaner” class of people in those who have been vaccinated.

Make-A-Wish Grants Wishes Only to Vaccinated Children?

Make-A-Wish is a nonprofit organization that’s well-known for granting wishes, such as travel or meetings with celebrities, to children with critical illnesses. However, a widely circulated video featured Make-A-Wish Foundation CEO Richard Davis stating that certain wishes would only be granted to vaccinated children and families:¹

“I’m excited to share that Make-A-Wish will resume granting air travel wishes within the United States and its territories, as well as granting wishes involving large gatherings, for vaccinated Wish families as soon as September 15, 2021.

All Wish participants, including your Wish kid and any siblings, will need to be two weeks past completion of either a one-dose or a two-dose vaccine.

While we won’t ask for proof of vaccination, we’ll ask for any adult participant to sign a letter of understanding that certifies that they, and any minors participating in the wish, are vaccinated and understand the risks of traveling at this time.”

Backlash quickly ensued, not only because of the discrimination against those who choose not to get vaccinated, but also because children under 12 cannot be vaccinated for COVID-19 at this time, and even those within the eligible age range may be too ill to be vaccinated. Celebrities such as actor Rob Schneider said that if Make-A-Wish wasn’t going to grant wishes to unvaccinated children, they would no longer support the organization.²

In response, Make-A-Wish backpedaled their statements, claiming that “misinformation and falsehoods on social media and in some media outlets” took the comments out of context and led to the confusion.³ In an updated statement Make-A-Wish clarified that all critically ill children are eligible, including those who are unvaccinated:⁴

“We understand that there are many families whose children aren't eligible for the vaccine yet, and we also know that there are families who are choosing to not get the vaccine. We respect everyone’s freedom of choice. Make-A-Wish will continue to grant wishes for all eligible children. Make-A-Wish will not require anyone to get vaccinated to receive a wish.”

Dating Apps Give Premium Content to Vaccinated

In 2021, it’s not enough to divulge your likes and dislikes to get a date — you’ve also got to display personal medical data, like whether or not you’ve been vaccinated.

Dating app giants including Tinder, Hinge, OKCupid, BLK, Chispa, Plenty of Fish, Match, Bumble and Badoo now allow users to filter matches according to vaccination status and also announced that those who are vaccinated will get access to premium content such as “like boosts, super likes, and super swipes” — but only with proof of vaccination.⁵

The move comes via an unlikely partnership with the White House, which is targeting dating apps in an effort to increase COVID-19 vaccinations in the U.S.

“We believe that it’s particularly important to reach young people where they are in the effort to get them vaccinated,” a White House press release noted. They cited OKCupid, which reported that people who display their vaccination status are 14% more likely to get a match. Further, according to the White House:⁶

“Social distancing and dating were always a bit of a challenging combination. So today, dating sites like Bumble, Tinder, Hinge, Match, OkCupid, BLK, Chispa, Plenty of Fish, and Badoo are announcing a series of features to encourage vaccinations and help people meet people who have that universally attractive quality: They’ve been vaccinated against COVID-19.

These sites cater to over 50 million people in the U.S. and are some of the world’s biggest nongaming apps … We have finally found the one thing that makes us all more attractive: a vaccination.

These dating apps will now allow vaccinated people to display badges which show their vaccination status, filter specifically to see only people who are vaccinated, and offer premium content — details of which I cannot get into, but apparently, they include things like boosts and super swipes. The apps will also help people locate places to get vaccinated.”

Concerts, Travel Only for the Vaccinated

Unvaccinated people are also being excluded from certain concert venues, including S. James Theater in New York City, which recently featured Bruce Springsteen. Jujamcyn, which operates the theater, stated that guests must be “fully vaccinated with an FDA or WHO approved vaccine in order to attend SPRINGSTEEN ON BROADWAY and must show proof of vaccination at their time of entry into the theatre with their valid ticket.”⁷

Exceptions were only made for people under the age of 16 or “those who need reasonable accommodations due to a disability or sincerely held religious belief.” Protestors arrived to the show’s opening night, with signs stating "no vax passports" and "Bruce Springsteen is for segregation on Broadway.”⁸

Protestors also arrived outside a Foo Fighters concert at the Canyon Club in Agoura Hills, California, which was also closed to unvaccinated fans. In addition to calling the vaccination requirement a form of segregation, one protestor told KCAL news, “Those of us who have healthy immune systems should be able to enjoy these freedoms just like anybody else.”⁹

In other examples of loss of privileges for the unvaccinated, in Hawaii only those with proof of vaccination are allowed to travel between counties without pretravel testing and quarantine restrictions, while New York requires you to be vaccinated or have a recent negative COVID-19 test to enter certain sports arenas and large performance venues.

If you’re planning to travel on a cruise ship, there are also different requirements depending on vaccination status. Royal Caribbean recently announced that unvaccinated guests would need proof of COVID-19 related travel insurance to board and would also be banned from certain areas of ships. On the Freedom of the Seas, for instance, unvaccinated travelers would not be able to enter certain spas, casinos, parties, pools, bars and restaurants.¹⁰

A Florida law prohibits Royal Caribbean from asking if guests are vaccinated, so to get around this anyone who doesn’t show proof of vaccination will be considered unvaccinated. The segregation of vaccinated and unvaccinated guests will be obvious, as those who are vaccinated will receive a wristband while those who are not will have a hole punched in the card needed to access certain areas of the ship.¹¹

In other cases, people have lost their jobs due to their vaccination choice, including at Houston Methodist hospital, where employees were forced to either resign or be fired if they chose not to get a COVID-19 vaccine.¹²

What About People With Natural Immunity?

A sizeable percentage of the population has made it clear that they have no intention of getting vaccinated with an experimental gene therapy. Everyone has their own reasons for this decision, including an unknown risk of side effects and death but, for some, their reasoning is that they’ve already had COVID-19 and therefore have natural immunity.

If protecting public health were really the ultimate goal in the pandemic response, people who have recovered from COVID-19 should be offered the same type of immunity “passports” and benefits being offered to those who have been vaccinated. In fact, they should be granted even more “access” since their immunity is likely superior to those with vaccine-induced immunity.

Evidence from Washington University School of Medicine shows long-lasting immunity to COVID-19 exists in those who’ve recovered from the natural infection.¹³ At both seven months and 11 months after infection, most of the participants had bone marrow plasma cells (BMPCs) that secreted antibodies specific for the spike protein encoded by SARS-CoV-2.

In addition, in 2020 it was reported that people who had recovered from SARS-CoV — a virus that is genetically closely related to SARS-CoV-2 and belongs to the same viral species — maintained significant levels of neutralizing antibodies as much as 17 years after initial infection.¹⁴ This also suggests that long-term immunity against SARS-CoV-2 should be expected,¹⁵ and natural protection is likely to continue “indefinitely.”¹⁶

This — natural immunity to COVID-19 that an unknown number of people have acquired — is completely ignored when it comes to official guidelines. Everyone is urged to get vaccinated with an experimental shot, regardless of their COVID-19 infection history and even if they’re as young as 12 years old — in some cases without parental consent.¹⁷

As Dr. Peter McCullough, vice chief of internal medicine at Baylor University Medical Center, has stated, "All roads lead to the vaccine,"¹⁸ and it’s possible the pandemic’s purpose was to fuel the global vaccination campaign that is now occurring. This would allow for the vaccinated population to be recorded in a vaccine database, essentially “marking” you, which could be used as a tool for population control via vaccine passports.

Vaccine Passports Will Open the Floodgates

Right now, we’re in a battle of freedom versus tyranny. Fortunately, a number of states have enacted laws that ban vaccine passport requirements in order to prevent the creation of a two-tier society based on vaccination status. It’s important to understand that the adoption of vaccine passports will only open the floodgates for further restrictions on your freedom.

The end goal here isn’t about tracking vaccination status only. Vaccine passports or any other type of tracking and tracing device or certification system are part of a much larger plan to implement a global social credit system based on 24/7 electronic surveillance to ensure compliance.

This will expand to include not just COVID-19 infection and vaccination status but also other medical data, basic identification records, financial data and just about anything else that can be digitized and tracked. There’s still time to take action to protect freedom as we know it today, and one of the best ways to do so is by speaking out via peaceful protest and civil disobedience.

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A research team performs machine learning-powered photoacoustic/ultrasound imaging for thyroid cancer classification.

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Babies younger than four weeks old, called neonates, were once thought not to perceive pain due to not-yet-fully-developed sensory systems, but modern research says otherwise.

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Listening to vocal music is a simple and cost-efficient way of promoting recovery and brain health after a stroke.

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Recess quality, not just the amount of time spent away from the classroom, plays a major role in whether children experience the full physical, mental and social-emotional benefits of recess, a new study has found.

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Scientists investigated the efficiency of splicing across different human cell types. The results were surprising in that the splicing process appears to be quite inefficient, leaving most intronic sequences untouched as the transcripts are being synthesized. The study also reports variable patterns between the different introns within a gene and across cell lines, and it further highlights the complexity of how newly transcripts are processed into mature mRNAs.

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Investigators conducted a systematic review and meta-analysis of 38 randomized controlled trials of omega-3 fatty acids. Overall, they found that omega-3 fatty acids improved cardiovascular outcomes. Results showed a significantly greater reduction in cardiovascular risk in studies of EPA alone rather than EPA+DHA supplements.

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The world's largest study of global climate related mortality found deaths related to hot temperatures increased in all regions from 2000 to 2019, indicating that global warming due to climate change will make this mortality figure worse in the future. The international research team looked at mortality and temperature data across the world from 2000 to 2019, a period when global temperatures rose by 0.26C per decade.

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The CDC's Advisory Committee on Immunization Practices (ACIP) recently unanimously voted 14-0 to coadminister the COVID-19 and flu vaccine to adults and children.¹ The proposed policy for the 2021-2022 influenza season was made to implement changes that coincide with the timing of children returning to school in fall 2021, and to align with the CDC’s guidelines allowing COVID-19 vaccines to be coadministered with other vaccines.

This also will be the first influenza season² where nearly all available flu vaccines are quadrivalent,³ rather than trivalent. This means flu shots will contain four vaccine strain influenza viruses — two influenza A viruses and two influenza B viruses.

The ACIP vaccine policy recommendations also included explicit information about when influenza vaccines should be given to children and adults.⁴ For example, the recommendations direct vaccine providers to give non-pregnant adults flu shots after August because of concerns about waning vaccine-acquired artificial immunity.

Vaccine providers are directed to give children flu shots by the end of October, with the dog kidney (MDCK) cell-based Flucelvax quadrivalent vaccine now being recommended for children starting at age 2 and older.

The policy also calls for precautions in giving a vaccine to anyone with a moderate or severe acute illness, history of Guillain-Barré syndrome within six weeks of receiving an influenza vaccine, or a history of severe allergic reactions to any other dose of flu vaccine.⁵

Unanimous Vote: CDC Approved One Flu and COVID Vaccine

In addition to approving the coadministration of flu and COVID-19 vaccines, ACIP warns that providers should be aware their patients may exhibit increased reactogenicity. This is a term health authorities use to describe expected adverse reactions to pharmaceutical products, especially hyper-inflammatory immunological responses to vaccination.

The literature⁶ calls it a “physical manifestation of the inflammatory response to vaccination” and “symptoms may include pain, redness, swelling or induration for injected vaccines, and systemic symptoms, such as fever, myalgia, headache or rash.”

In other words, the CDC expects more people to experience side effects/adverse reactions when influenza and COVID-19 vaccines are administered concurrently. ACIP member Dr. Matthew Daly believes that this year “Most adolescents will be vaccinated [against] COVID-19 in the summer and have their flu vaccination in the fall.”⁷

But coadministration of the two vaccines next year could increase the number of children receiving COVID-19 vaccine together with influenza vaccine and, subsequently, potentially increase reactogenicity. In the same meeting, the committee also voted unanimously to recommend a shorter rabies vaccination series for children traveling to areas where the potential risk is high.

Lastly, ACIP recommended the dengue vaccine for children ages 9 to 16 who live in areas where the virus is endemic. According to the CDC,⁸ the dengue virus spreads through the bite of a mosquito, infecting up to 400 million people each year. Each year, nearly 100 million will get sick and 22,000 will die from dengue.

No Evidence to Suggest Concurrent Vaccination Policy Is Safe

Despite the unanimous vote by CDC health experts charged with protecting the health of U.S. citizens, there is no evidence to suggest that giving children or adults influenza and COVID-19 vaccines simultaneously on the same day is safe. Some ACIP members noted the lack of data proving that concurrent vaccination policy is safe.

However, Medpage⁹ reports that CDC staff countered by citing one preprint study¹⁰ — published just days before the ACIP meeting — that examined the safety issues and efficacy of coadministering flu vaccine with the Novavax COVID-19 vaccine.

With this study, CDC staff noted there were “no changes in antibody titers for influenza vaccine and no safety issues” when give in combination, although participants did have greater tenderness or pain at the injection site, and higher levels of fatigue and muscle pain.

It’s also crucial to note that the information on which they based this decision was gathered from a sub-study of just 217 participants who had fewer comorbid conditions and were younger than those in their vaccine’s main study.¹¹

Also important to note is that the experimental Novavax COVID-19 vaccine is a subunit protein,¹² which is different from the mRNA COVID-19 vaccines. This means that information from the Novavax study cannot be extrapolated to the experimental mRNA vaccines now being administered under an EUA.¹³

Unlike the messenger RNA vaccines, which use genetic material to trigger the body to make parts of the SARS-CoV-2 spike protein, the Novavax vaccine’s protein adjuvant contains the spike protein as a nanoparticle.¹⁴ The manufacturer proposes that it stimulates the immune system to recognize the virus and resist infection.

Additionally, none of the mRNA COVID-19 vaccines being distributed under an EUA has been tested for safety and efficacy when coadministered with influenza vaccine. In other words, the CDC made a recommendation that the two vaccines can be given simultaneously to children and adults without providing data conclusively demonstrating safety or efficacy.

Could Flu Vaccines Increase Risk of COVID-19?

Over the years, data have demonstrated that the flu vaccine has kept missing the mark when it comes to effectiveness. In the 2004-2005 season, the vaccine’s overall effectiveness was only 10%,¹⁵ which means 90% of the time it failed. During the 2012-2013 flu season it was 49% effective overall and in 2014-2015 it was only 19% effective overall.

The abysmal success rate of the seasonal influenza vaccines is related to how the vaccine is developed each year.¹⁶ Because influenza viruses are constantly mutating, the vaccine must be reviewed and updated to include those the scientists estimate will be circulating in the coming flu season.

Each year, 100 centers in over 100 countries conduct surveillance, which includes testing thousands of influenza virus samples from patients. Twice a year these results are analyzed, and the World Health Organization recommends the specific viruses that should be included in the coming year’s influenza vaccine. In America, the FDA makes the final decision.

In other words, scientists must guess based on past data which influenza viruses will be circulating in the upcoming season. There is also evidence from Canadian studies¹⁷ that with repeated vaccinations, flu vaccine effectiveness wanes. This type of study will not be done in the U.S. for the simple reason that U.S. authorities recommend everyone get vaccinated every year. As noted by STAT news:¹⁸

"Given that policy, it would be unethical for researchers here to randomly assign some people to forgo vaccinations in some years. But experts elsewhere, including in Hong Kong, where influenza circulates year-round, are trying to put together the funding for what would have to be a large, multiyear study."

The SARS-CoV-2 virus that causes COVID-19 also mutates and is expected to continue to mutate in the environment, resulting in new strain variants. Additionally, a study published in January 2020 in the journal Vaccine¹⁹ found that people who had received influenza vaccines during the 2017-2018 flu season were more likely to get some form of coronavirus infection.

When compared to unvaccinated individuals, those who had gotten the seasonal flu shot were 36% more likely to contract an unspecified coronavirus infection and 51% more likely to contract human metapneumovirus, which has respiratory symptoms similar to COVID-19.

In October 2020,²⁰ another positive association was found between COVID-19 deaths and flu vaccination rates in the elderly. This means coadministration of these vaccines may have potentially serious side effects.

An analysis of data²¹ from 39 countries with more than one-half million inhabitants showed that those over 65 years old who had gotten a flu shot had an increased risk of death from COVID-19. An analysis published in May 2020²² looked at European countries with the highest COVID-19 death rates and found those countries also had the highest rate of influenza vaccinations among the elderly.

Why COVID-19 Vaccine for Children Is Very Risky

There is no evidence that coadministration of influenza vaccine and COVID vaccine is safe, but there is evidence that giving the COVID-19 vaccine to children is extremely risky. A video entitled “Why Children Should Not Receive the COVID Shot,” features comments that Peter Doshi, Ph.D., made during a June 10, 2021, meeting of the FDA’s Vaccines and Related Biological Products Advisory Committee.

Doshi is the senior editor of The BMJ and associate professor at the University of Maryland School of Pharmacy. In a paper published in The BMJ, he points out that Pfizer's claim the vaccine is 95% effective refers to relative risk reduction. The absolute risk reduction is actually less than 1%.²³

In addition, the primary endpoint measured is a reduction in severity and not the vaccine's ability to prevent infection or save lives. The decision to vaccinate should be made on a risk-benefit analysis, where the benefit far outweighs the potential risks involved.

However, as I discussed in the linked article above, the benefits are rare, the side effects are common, and the long-term effects are completely unknown. For example, Pfizer boasts a 100% efficacy rate in the 12-to-15 age group. In the video, Doshi explains this was based on less than 2% of the placebo group getting COVID-19, while none in the fully vaccinated group got sick.

As reported in The Defender,²⁴ many of the side effects have been short-lived but, by June 11, 2021, there were 6,332 total adverse events in 12- to 17-year-olds, seven deaths and 271 events rated “serious.”

According to OpenVAERS²⁵ one week later, data through June 18, 2021, showed 11,584 adverse events and nine deaths in the same age group. In one week, there were two more deaths and 5,252 more adverse events reported to OpenVAERS.

One of the reasons health experts give for vaccinating children, many of whom Doshi explains have natural immunity from a COVID-19 infection, is to benefit adults. This practice is sometimes called “cocooning” and has never been proven to be effective.

The authors of an editorial in The BMJ²⁶ stressed that giving children COVID-19 vaccine is “hard to justify right now” since children experience mild disease symptoms and transmission is limited, while the potential for unintended consequences from the vaccine is high. They go on to write:

“Should childhood infection (and re-exposures in adults) continue to be typically mild, childhood vaccination will not be necessary to halt the pandemic. The marginal benefits should therefore be considered in the context of local healthcare resources, equitable distribution of vaccines globally, and a more nuanced understanding of the differences between vaccine and infection induced immunity.

Once most adults are vaccinated, circulation of SARS-CoV-2 may in fact be desirable, as it is likely to lead to primary infection early in life when disease is mild, followed by booster re-exposures throughout adulthood as transmission blocking immunity wanes but disease blocking immunity remains high. This would keep reinfections mild and immunity up to date.”

How to Report a Vaccine Reaction

The number of vaccines recommended by health authorities for children has grown significantly in the past decades.²⁷ The CDC’s childhood vaccine schedule recommends all children receive 69 doses of 16 vaccines with 50 doses of 14 vaccines given between the day of birth and age 18. The majority of children in the U.S. today receive three times as many vaccinations as children received in 1983.

If you or your child gets a COVID-19 vaccine and your health deteriorates within hours, days or weeks of being vaccinated, the medical professional who gave you the shot is required to file a report with the federal vaccine adverse event reporting system (VAERS).²⁸

Despite the VAERS having been established in 1990²⁹ and used for over 30 years, Dr. Anne Schuchat from the CDC said in an interview with ABC News³⁰ that one of the reasons for pausing the Johnson & Johnson COVID-19 vaccine was to teach vaccine providers how to report adverse events to VAERS.

Since the experimental COVID-19 vaccines currently are being distributed under an Emergency Use Authorization (EUA) granted to vaccine manufacturers by the FDA) there is a great need to report vaccine reactions, especially injuries and deaths. If your health care provider refuses to file an injury report with VAERS, the system allows you to do it yourself.

As of June 18, 2021, the system shows there have been 6,136 deaths, 21,806 people hospitalized and 51,575 people seen in urgent care after receiving a COVID-19 vaccination. Additionally, the system highlights these injuries:³¹

Reported Injury	Number
Life threatening reactions	6,450
Heart attack	2,483
Myocarditis or pericarditis	1,644
Low platelet count	1,776
Miscarriage	720
Severe allergic reactions	17,408
Disabled	5,194
Tinnitus (ringing in the ear)	4,447

You can report a adverse reaction to a COVID-19 vaccine, or to any other vaccine, to the VAERS system.^32,33 There are two ways to make a report — online or through a writable PDF form that can be uploaded to the system. If you have any questions call 1-800-822-7967.

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So much has happened over the past year that it may be hard to remember what life was like pre-COVID. But let’s flash back to December 2019, when the idea of social distancing, compulsory masking and lockdowns would have been met with disbelief and outrage by most Americans.

At that time, most were blissfully unaware of the pandemic that would change the world in the next few months. It wasn’t until December 31, 2019, that the COVID-19 outbreak was first reported from Wuhan, China,¹ and at this point it was only referred to as cases of viral pneumonia, not a novel coronavirus.² I say “most” because it seems some people may have been aware of something lurking much earlier than it appeared.

In confidential documents³ revealed by the U.K.’s Daily Expose, Moderna, together with the National Institute of Allergy and Infectious Diseases (NIAID), sent mRNA coronavirus vaccine candidates to the University of North Carolina at Chapel Hill December 12, 2019 — raising significant red flags. As The Daily Expose reported:⁴

“What did Moderna [and NIAID] know that we didn’t? In 2019 there was not any singular coronavirus posing a threat to humanity which would warrant a vaccine, and evidence suggests there hasn’t been a singular coronavirus posing a threat to humanity throughout 2020 and 2021 either.”

COVID-19 Vaccine Candidate Was Released Prior to Pandemic

The confidential disclosure agreement relays a material transfer agreement between the providers — Moderna, NIAID and the National Institutes of Health (NIH) — and the University of North Carolina at Chapel Hill. The providers agreed to transfer “mRNA coronavirus vaccine candidates developed and jointly-owned by NIAID and Moderna” to the university’s investigator.⁵

“The material transfer agreement was signed the December 12th 2019 by Ralph Baric, PhD, at the University of North Carolina at Chapel Hill, and then signed by Jacqueline Quay, Director of Licensing and Innovation Support at the University of North Carolina on December 16th 2019,” Daily Expose noted.

At this point, some backstory information is more than relevant. We know with great certainty that researchers at China’s Wuhan Institute of Virology (WIV) had access to and were doing gain-of-function research on coronaviruses, and manipulating them to become more infectious and to more easily infect humans. We also know that they collaborated with scientists in the U.S. and received funding from the National Institutes of Health for such research.

Baric, who signed the material transfer agreement to investigate the mRNA coronavirus vaccine candidate before there was a known COVID-19 pandemic, pioneered techniques for genetically manipulating coronaviruses, according to Peter Gøtzsche with the Institute for Scientific Freedom,⁶ and these became a major focus for WIV.

Baric worked closely with Shi Zhengli, Ph.D., the director of WIV’s Center for Emerging Infectious Diseases, also known as “bat woman,” on research using genetic engineering to create a “new bat SARS-like virus ... that can jump directly from its bat hosts to humans.” According to Gøtzsche:⁷

“Their work focused on enhancing the ability of bat viruses to attack humans so as to ‘examine the emergence potential.’ In 2015, they created a novel virus by taking the backbone of the SARS virus replacing its spike protein with one from another bat virus known as SHC014-CoV. This manufactured virus was able to infect a lab culture of cells from the human airways.

They wrote that scientific review panels might deem their research too risky to pursue but argued that it had the potential to prepare for and mitigate future outbreaks. However, the value of gain-of-function studies in preventing the COVID-19 pandemic was negative, as this research highly likely created the pandemic.”

Moderna Gets Emergency Use Approval for COVID Vaccines

The rest of the story, as the saying goes, is history. December 12, 2019, Amy Petrick, Ph.D., NIAID’s technology transfer specialist, signed the agreement, along with Dr. Barney Graham, an investigator for NIAID, whose signature is undated.⁸ May 12, 2020, just months later, Moderna was granted a fast-track designation for its mRNA-1273 vaccine by the U.S. Food and Drug Administration. According to Moderna’s news release:⁹

“mRNA-1273 is an mRNA vaccine against SARS-CoV-2 encoding for a prefusion stabilized form of the Spike (S) protein, which was selected by Moderna in collaboration with investigators from Vaccine Research Center (VRC) at the National Institute of Allergy and Infectious Diseases (NIAID), a part of the NIH.”

December 18, 2020 — about one year after the material transfer agreement was signed — the FDA issued emergency use authorization for Moderna’s COVID-19 vaccine for use in individuals 18 years of age and older.¹⁰ June 10, 2021, Moderna also filed for emergency use authorization for its COVID-19 shot to be used in U.S. adolescents aged 12 to 17 years.¹¹ Yet, we still have no answers to some glaring questions:¹²

“It was not until January 9th 2020 that the WHO reported¹³ Chinese authorities had determined the outbreak was due to a novel coronavirus which later became known as SARS-CoV-2 with the alleged resultant disease dubbed COVID-19. So why was an mRNA coronavirus vaccine candidate developed by Moderna being transferred to the University of North Carolina on December 12th 2019?

… Perhaps Moderna and the National Institute of Allergy and Infectious Diseases would like to explain themselves in a court of law?”

SARS-CoV-2 Appears To Be Uniquely Able to Infect Humans

Nikolai Petrovsky, professor of endocrinology at Flinders University College of Medicine in Adelaide, Australia, is among those who has stated SARS-CoV-2 appears to be optimally designed to infect humans.¹⁴

His team sought to identify a way by which animals might have comingled to give rise to SARS-CoV-2, but concluded that it could not be a naturally occurring virus. Petrovsky has previously stated it appears far more likely that the virus was created in a laboratory without the use of genetic engineering, by growing it in different kinds of animal cells.¹⁵

To adapt the virus to humans, it would have been grown in cells that have the human ACE2 receptor. Over time, the virus would then adapt and eventually gain the ability to bind to the human receptor. U.S. Right to Know (USRTK) pointed out that the issue of binding sites is an important one, as the distinctive binding sites of the SARS-CoV-2 spike protein "confer 'near-optimal' binding and entry of the virus into human cells."¹⁶

Scientists have argued that SARS-CoV-2's unique binding sites may be the result of either natural spillover in the wild or deliberate recombination of an unidentified viral ancestor. Baric and others, including Peter Daszak, EcoHealth Alliance president, to which he is closely tied, were quick to dismiss the lab-leak hypothesis, which suggests that SARS-CoV-2 accidently leaked from a laboratory in Wuhan, China. Yet, according to Gøtzsche:¹⁷

“On 9 December 2019, just before the outbreak of the pandemic, Daszak gave an interview in which he talked in glowing terms of how his researchers at the Wuhan Institute had created over 100 new SARS- related coronaviruses, some of which could get into human cells and could cause untreatable SARS disease in humanized mice … ”

Daszak’s EcoHealth Alliance funded controversial GOF research at WIV; NIAID gave funding to the EcoHealth Alliance, which then funneled it to WIV.¹⁸ Daszak, despite working closely with WIV, was part of the World Health Organization’s investigative team charged with identifying the origin of SARS-CoV-2. Not surprisingly, the team dismissed the lab-accident theory.

Baric’s SARS-Like Virus Wasn’t Made Public Until May 2020

Regarding the novel SARS-like virus that Shi and Baric created in 2015, this research was conducted using a grant from EcoHealth Alliance.

While the information relating to the virus’ DNA and RNA sequences was supposed to have been submitted to a national biotechnology information database when the research was published, this wasn’t done until years later, in the midst of the COVID-19 pandemic. As reported by Alexis Baden-Mayer, political director for the Organic Consumers Association:¹⁹

“The work, ‘A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence,’²⁰ published in Nature in 2015 during the NIH’s moratorium²¹ on gain-of-function research, was grandfathered in because it was initiated before the moratorium … 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, requires²² 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 deposited²³ in GenBank until May 2020.”

Meanwhile, both Baric²⁴ and Daszak were involved in organizing the publication of a scientific statement, published in The Lancet and signed by 26 additional scientists, condemning inquiries into the lab-leak hypothesis as “conspiracy theory.”²⁵

Daszak was also made a commissioner of the Lancet Commission on COVID-19, but now that his extreme conflict of interest has been made public, he was recused from the commission.²⁶

Baric, Daszak Downplay Lab-Leak Theory

At the time The Lancet statement was released in February 2020, Daszak had advised Baric against adding his signature because he wanted to “put it out in a way that doesn't link it back to our collaboration so we maximize an independent voice.”²⁷ The authors also declared no competing interests.

In an update published June 21, 2021, The Lancet stated, “Some readers have questioned the validity of this disclosure, particularly as it relates to one of the authors, Peter Daszak.”²⁸ The journal invited the authors to “re-evaluate their competing interests,” and Daszak suddenly had much more to say. His updated disclosure statement reads, in part:²⁹

“EcoHealth Alliance's work in China includes collaboration with a range of universities and governmental health and environmental science organizations, all of which are listed in prior publications, three of which received funding from US federal agencies as part of EcoHealth Alliance grants or cooperative agreements, as publicly reported by NIH.

… EcoHealth Alliance's work in China involves assessing the risk of viral spillover across the wildlife–livestock–human interface, and includes behavioral and serological surveys of people, and ecological and virological analyses of animals.

This work includes the identification of viral sequences in bat samples, and has resulted in the isolation of three bat SARS-related coronaviruses that are now used as reagents to test therapeutics and vaccines.

It also includes the production of a small number of recombinant bat coronaviruses to analyze cell entry and other characteristics of bat coronaviruses for which only the genetic sequences are available.”

Also of note, a special review board, the Potential Pandemic Pathogens Control and Oversight (P3CO) committee, was created within the Department of Health and Human Services to evaluate whether grants involving dangerous pathogens are worth the risks.

Baden-Mayer explained, “This committee was set up as a condition for lifting the 2014-2017 moratorium on gain-of-function research. The P3CO committee operates in secret. Not even a membership list has been released.”³⁰

Daszak stated in his updated disclosure, “NIH reviewed the planned recombinant virus work and deemed it does not meet the criteria that would warrant further specific review by its Potential Pandemic Pathogen Care and Oversight (P3CO) committee.”³¹

However, according to Rutgers University professor Richard Ebright, an NIH grant for research involving the modification of bat coronaviruses at the WIV was sneaked through because the NIAID didn’t flag it for review.³² In other words, the WIV received federal funding from the NIAID without the research first receiving a green-light from the HHS review board.

The NIAID apparently used a convenient loophole in the review framework. As it turns out, it’s the funding agency’s responsibility to flag potential GOF research for review. If it doesn’t, the review board has no knowledge of it. According to Ebright, the NIAID and NIH have “systemically thwarted — indeed systematically nullified — the HHS P3CO Framework by declining to flag and forward proposals for review.”³³

Who Knew What, and When?

We now have proof that Moderna and NIAID sent their mRNA coronavirus vaccine candidates to Baric at the University of North Carolina at Chapel Hill in mid-December 2019. Were they aware that COVID-19 was circulating at that time, or did they have knowledge far before that such a vaccine would soon be in demand? The red flags, and cover-ups, continue to mount, but ultimately the truth will prevail.

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