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COVID-19

The Federal Government Paid Media Outlets to Promote the Covid Vaccine

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11 minute read

From the Brownstone Institute

BY Rav AroraRAV ARORA

After releasing my three-part series earlier this year showing how multiple media outlets refused to platform dissent on the Covid vaccine, I was asked on multiple podcasts why this was the case. Ideological groupthink, fear of exacerbating institutional distrust, and financial motives were on my list of potential explanations, but I did not have concrete evidence.

As I highlighted in my first piece, the responses I got from editors claiming their publication’s “pro-vaccine” allegiance was quite jarring. More than anything else, a publication should be “pro-truth” — whether that means highlighting the astounding benefits of a therapeutic or exposing its serious side effects. The idea that a whole media corporation would take a firm stance on a novel, experimental product is antithetical to the core purpose of journalism.

As I’ve said many times before, we are a pro-vaccination newspaper, and personally I just wish everyone would get vaccinated already.

Editor response to Rav Arora’s story proposals on vaccine risks

As it turns out, mainstream media’s nearly monolithic coverage of mRNA vaccines and other Covid measures can be at least partially explained by a clear financial interest. Recently, independent journalist Breanna Morello — who left Fox News because of draconian vaccine mandates in New York City — alerted me to a FOIA request filed by the conservative media company TheBlaze, which found a number of major media outlets were paid to promote the Covid vaccine.

Such venues included the Washington PostLos Angeles Times, NBC, CNN, Fox News, and several others. TheBlaze’s report received little coverage — even in conservative media (perhaps because some of those outlets were also paid by HHS) ideologically predisposed to criticize government-fuelled narratives on the pandemic. As The Blaze reports:

Hundreds of news organizations were paid by the federal government to advertise for the vaccines as part of a “comprehensive media campaign,” according to documents TheBlaze obtained from the Department of Health and Human Services. The Biden administration purchased ads on TV, radio, in print, and on social media to build vaccine confidence, timing this effort with the increasing availability of the vaccines.

During the vaccine rollout, the Biden administration made a number of efforts to bolster vaccination rates. The US Department of Health and Human Services’ COVID-19 Public Education Campaign states they employed “both paid advertising and media interviews, presentations, radio/TV tours, and other public events to educate people about the importance of vaccination.”

The L.A Times – an outlet funded by HHS to promote Covid vaccines – runs a morally reprehensible column justifying mockery of ‘anti-vaxxer’ deaths.

The HHS website contains public access to all vaccine campaign advertisements for media outlets and beyond. One past advertisement promotes Covid vaccination in children, featuring a montage of selected medical doctors stating in unison,

We can all agree on this: you can trust the Covid vaccine for yourself, or your kids, or your grandkids….I mean it from the heart.

In another ad directed to parents, HHS’ selection of doctors state,

We want you to know, Covid vaccines are ‘safe and effective’.’ My grandkids are vaccinated…what’s not safe is getting Covid.

Is it ethical for the government to dubiously claim Covid vaccines are uniformly beneficial for kids, and contracting Covid is far less “safe” than getting your child double-vaccinated? No such randomized clinical evidence exists suggesting the benefits of the Covid vaccine outweigh the harms in young cohorts with a nearly zero risk of serious outcomes. The concentrated risk of myocarditis in boys and menstrual irregularities in girls suggest the Covid vaccine may be harmful on net. Moreover, is it ethical (for either party) for the federal government to advertise such medical misinformation on platforms allegedly committed to investigating the truth and holding the powerful accountable?

HHS advertisement on the updated Covid booster

A new government ad on the HHS website now promotes the updated Covid vaccine. It falsely claims the new booster shot prevents long Covid and hospitalization when the only available evidence from Pfizer and Moderna are rat studies and a 50-person trial (with an unexplained 2% rate of serious adverse events).

Rather than critically covering such propagandistic attempts to promote a longitudinally ineffective therapeutic with a 1 in 800 serious adverse event rate, major media outlets allowed the federal government to freely spread its misinformation on their platform. The New York Times’ reporting on vaccine-induced myocarditis, for example, downplayed the side effect at every sight and compared it to misleadingly higher rates of Covid-induced myocarditis:

For over two years, the media and government officials have been peddling dangerous misinformation — the very sin they accuse of the conspiracy web of committing — about COVID-19 posing a higher risk to young people than the vaccine. Instead of examining age, gender, and health-stratified risk-benefit ratios, they elementarily look at aggregate data and cherry-pick seemingly beneficial outcomes to justify their “Everyone should get vaccinated!” campaign. A few of umpteen examples:

CNBC: “Myocarditis risk higher after Covid infection than Pfizer or Moderna vaccination, CDC finds

Reuters: “Higher risk of heart complications from COVID-19 than vaccines -study”

CNN: “Pediatric cardiologists explain myocarditis and why your teen should still get a Covid-19 vaccine

The Conversation: “Myocarditis: COVID-19 is a much bigger risk to the heart than vaccination

As an admittedly biased Zoomer, one of the most discrediting media assault campaigns grew in opposition to Joe Rogan’s claim in a June 2021 podcast that healthy 21-year-olds didn’t need the vaccine. Over two years later, Rogan’s judgment has been vindicated — as it was at the time — given the 0.003% mortality risk among 20-year-olds and unusually high rates of myocardial and menstrual-related vaccine adverse events. However, the mainstream media ecosystem conducted a fierce reputational decapitation in response to Rogan’s impermissible dissent from the CDC and Pfizer’s edicts:

The Washington PostJoe Rogan is using his wildly popular podcast to question vaccines. Experts are fighting back.

The AtlanticJoe Rogan’s Show May Be Dumb. But Is It Actually Deadly?

Today: Dr. Fauci says Joe Rogan ‘incorrect’ to tell young people not to get vaccinated

NBC: Joe Rogan’s Covid vaccine misinfo matters

The United States wasn’t alone in spending large sums of taxpayer dollars to promote its agenda. The Trudeau government invested over $600,000 in hiring social media influencers to advance federal directives, including the push for Canadians to get vaccinated and boosted.

As CTV reports, Health Canada spent the most on hiring influencers to promote government information; $130,600 was spent towards an “influencer campaign in support of the COVID-19 vaccination marketing and advertising campaign.”

None of this is to mention Pfizer’s vaccine campaigns paying celebrities to rhapsodize about marvellously ‘safe and effective’ mRNA inoculation. Travis Kelce — a professional football player watched and revered by many young American men in particular — promoted getting the updated booster shot and flu vaccine in the same visit.

The journalists I grew up admiring — such as Megyn Kelly, Glenn Greenwald, Alex Berenson (Unreported Truths), and Matt Taibbi (Racket News) — were known for challenging consensus and providing novel perspectives on complex sociopolitical topics. I relied on select journalistic outlets and individual commentators for an honest, independent evaluation of the facts.

The heavily biased coverage of race relations and criminal justice issues in 2020 following the tragic death of George Floyd was self-discrediting but hardly surprising given the dominance of identity politics in elite liberal discourse.

The deterioration of journalistic standards during the vaccine rollout beginning in 2021, however, was particularly disorienting. The Washington Post, NBC, and the New York Times should have held the Biden administration’s feet to the fire for promoting experimental vaccines in all Americans irrespective of risk and continued revelations regarding concerning side effects.

They miserably failed to do so.

The last standing bulwark against government propaganda and censorship is crumbling before our eyes, losing relevance by the month. Perhaps a solution for media institutions to earn back credibility is to critically cover federal agencies misinforming the public rather than take funds to promote their agendas.

Just a thought.

Republished from the author’s Substack

Author

  • Rav Arora

    Rav Arora is an independent journalist based in Vancouver, Canada.

COVID-19

USAID directed over $200 million to gain of function research leading up to SARS-CoV outbreak

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By John Leake

USAID gave Peter Daszak’s EcoHealth Alliance $207 million between 2009 and October 2019, right when SARS-COv-2 began to spread

With revelations emerging about USAID’s spending spree on friends and pet projects, I was reminded of the following April 2023 exchange between Senator Rand Paul and Samantha Power, Administrator of USAID from 2021 to 2025. I vividly remember the vexation I felt as I listened to the recording on my evening jog the next day. Note how she repeatedly looks Senator Paul directly in the eye and insists that USAID has disclosed the grant documents he has repeatedly requested, even though he repeatedly admonishes her that he KNOWS she isn’t telling him the truth because he has never seen them.

Note as well that in October 2019, when USAID officially ceased funding PREDICT, papers like the New York Times lamented that, bereft of such funds, the program would not be able to predict emerging infectious diseases.

A great deal of evidence indicates that this was precisely the time it became apparent that a novel SARS coronavirus was circulating in Wuhan, almost certainly the result of GoF research conducted as part of the PREDICT program.

In other words, PREDICT predicted nothing—it actually created the monster.

Yet another irony was a letter that Elizabeth Warren—the Supreme Self-Righteous Bloviator of the Senate (SSBS)—wrote on January 20, 2020 to the then Administrator Mark Green, demanding to know why PREDICT funding had been cut off.

I would bet a considerable sum that at least someone in USAID knew in October 2019 about the circulating monster that PREDICT had created with the assistance of the $207 million the agency had given the program over a ten year period.

The evidence is clear: USAID has long been a rogue agency that should indeed be brought under direct State Department Control with new, stringent transparency requirements about its activities and long prison times for people like Samantha Power who conceal the agency’s activities and then lie to Senators about them.

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Brownstone Institute

FDA Lab Uncovers Excess DNA Contamination in Covid-19 Vaccines

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From the Brownstone Institute

By 

An explosive new study conducted within the US Food and Drug Administration’s (FDA) own laboratory has revealed excessively high levels of DNA contamination in Pfizer’s mRNA Covid-19 vaccine.

Tests conducted at the FDA’s White Oak Campus in Maryland found that residual DNA levels exceeded regulatory safety limits by 6 to 470 times.

The study was undertaken by student researchers under the supervision of FDA scientists. The vaccine vials were sourced from BEI Resources, a trusted supplier affiliated with the National Institute of Allergy and Infectious Diseases (NIAID), previously headed by Anthony Fauci.

Recently published in the Journal of High School Science, the peer-reviewed study challenges years of dismissals by regulatory authorities, who had previously labelled concerns about excessive DNA contamination as baseless.

The FDA is expected to comment on the findings this week. However, the agency has yet to issue a public alert, recall the affected batches, or explain how vials exceeding safety standards were allowed to reach the market.

The Methods

The student researchers employed two primary analytical methods:

  • NanoDrop Analysis – This technique uses UV spectrometry to measure the combined levels of DNA and RNA in the vaccine. While it provides an initial assessment, it tends to overestimate DNA concentrations due to interference from RNA, even when RNA-removal kits are utilised.
  • Qubit Analysis – For more precise measurements, the researchers relied on the Qubit system, which quantifies double-stranded DNA using fluorometric dye.

Both methods confirmed the presence of DNA contamination far above permissible thresholds. These findings align with earlier reports from independent laboratories in the United StatesCanada, AustraliaGermany, and France.

Expert Reaction

Kevin McKernan, a former director of the Human Genome Project, described the findings as a “bombshell,” criticizing the FDA for its lack of transparency.

“These findings are significant not just for what they reveal but for what they suggest has been concealed from public scrutiny. Why has the FDA kept these data under wraps?” McKernan questioned.

CSO and Founder of Medicinal Genomics

While commending the students’ work, he also noted limitations in the study’s methods, which may have underestimated contamination levels.

“The Qubit analysis can under-detect DNA by up to 70% when enzymes are used during sample preparation,” McKernan explained. “Additionally, the Plasmid Prep kit used in the study does not efficiently capture small DNA fragments, further contributing to underestimation.”

In addition to genome integration, McKernan highlighted another potential cancer-causing mechanism of DNA contamination in the vaccines.

He explained that plasmid DNA fragments entering the cell’s cytoplasm with the help of lipid nanoparticles could overstimulate the cGAS-STING pathway, a crucial component of the innate immune response.

“Chronic activation of the cGAS-STING pathway could paradoxically fuel cancer growth,” McKernan warned. “Repeated exposure to foreign DNA through COVID-19 boosters may amplify this risk over time, creating conditions conducive to cancer development.”

Adding to the controversy, traces of the SV40 promoter were detected among the DNA fragments. While the authors concluded that these fragments were “non-replication-competent” meaning they cannot replicate in humans, McKernan disagreed.

“To assert that the DNA fragments are non-functional, they would need to transfect mammalian cells and perform sequencing, which wasn’t done here,” McKernan stated.

“Moreover, the methods used in this study don’t effectively capture the full length of DNA fragments. A more rigorous sequencing analysis could reveal SV40 fragments several thousand base pairs long, which would likely be functional,” he added.

Regulatory Oversight under Scrutiny

Nikolai Petrovsky, a Professor of Immunology and director of Vaxine Pty Ltd, described the findings as a “smoking gun.”

“It clearly shows the FDA was aware of these data. Given that these studies were conducted in their own labs under the supervision of their own scientists, it would be hard to argue they were unaware,” he said.

Nikolai Petrovsky, Professor of Immunology and Infectious Disease at the Australian Respiratory and Sleep Medicine Institute in Adelaide

Prof Petrovsky praised the quality of work carried out by the students at the FDA labs.

“The irony is striking,” he remarked. “These students performed essential work that the regulators failed to do. It’s not overly complicated—we shouldn’t have had to rely on students to conduct tests that were the regulators’ responsibility in the first place.”

The Australian Therapeutic Goods Administration (TGA), which has consistently defended the safety of the mRNA vaccines, released its own batch testing results, claiming they met regulatory standards. However, Prof Petrovsky criticised the TGA’s testing methods.

“The TGA’s method was not fit for purpose,” he argued. “It didn’t assess all the DNA in the vials. It only looked for a small fragment, which would severely underestimate the total amount of DNA detected.”

Implications for Manufacturers and Regulators

Now that DNA contamination of the mRNA vaccines has been verified in the laboratory of an official agency and published in a peer-reviewed journal, it becomes difficult to ignore.

It also places vaccine manufacturers and regulators in a precarious position.

Addressing the contamination issue would likely require revising manufacturing processes to remove residual DNA, which Prof Petrovsky explained would be impractical.

“The only practical solution is for regulators to require manufacturers to demonstrate that the plasmid DNA levels in the vaccines are safe,” Prof Petrovsky stated.

“Otherwise, efforts to remove the residual DNA would result in an entirely new vaccine, requiring new trials and effectively restarting the process with an untested product.”

Now the onus is on regulators to provide clarity and take decisive action to restore confidence in their oversight. Anything less risks deepening the scepticism of the public.

Both the US and Australian drug regulators have been approached for comment.

Republished from the author’s Substack

Author

Maryanne Demasi, 2023 Brownstone Fellow, is an investigative medical reporter with a PhD in rheumatology, who writes for online media and top tiered medical journals. For over a decade, she produced TV documentaries for the Australian Broadcasting Corporation (ABC) and has worked as a speechwriter and political advisor for the South Australian Science Minister.

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