Saturday, July 19, 2025

Polaris of Enlightenment

British PM confronted over vaccine injuries

The criticized covid vaccinations

Published 17 February 2024
– By Editorial Staff
2 minute read

At the GB News People’s Forum, a member of the audience took the opportunity to confront British prime minister Rishi Sunak. The man demanded that the Prime Minister look him in the eye to see his “pain, trauma and regret” for taking the covid vaccine and said that there was no real political concern for those harmed by the drug.

– My name is John Watt and I am one of the covid vaccine victims in this country, the man told Sunak at the GB News event, which was attended by what was described as a cross-section of British voters.

Watt went on to say that he knew people who had lost legs and suffered heart problems after taking the covid vaccine, and described the protection mechanisms for those injured by the shots as deeply flawed.

– I want you to look into my eyes. I want you to see the pain and the trauma and the regret in my eyes, he said.

– How is it that those in power who urged us to ‘do the right thing’ have now left us all to rot? he asked. Watt continued.

Sunak said that there are compensation programs for those injured by covid vaccines and that he could not comment on “individual cases”. The Premier also said that it was news to him that vaccine victims had been silenced, stating that it was “sad to hear”.

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Pharmaceutical giant’s top researcher on covid vaccine: “Nothing was safe and effective”

The criticized covid vaccinations

  • Joshua Rys, a leading regulatory researcher at pharmaceutical giant Johnson & Johnson (J&J), now confirms on hidden camera what mainstream media dismissed as "conspiracy theories".
  • "Do you have any idea the lack of research that was done on those products?" Rys asks rhetorically in the clip, among other things.
  • The slogans "safe and effective" that surrounded the mass vaccination campaign were, in his view, a direct lie from the authorities.
  • "This was just, let's test it on some lab route models, analyze and see if it works and stuff like that, and just roll it to the wind and see what happens", he adds.
Published 16 July 2025
– By Editorial Staff
The hidden recording confirms many concerns that have surrounded the COVID vaccines.
1 minute read

Joshua Rys leads the creation and implementation of regulatory strategies for new and existing products within Johnson & Johnson in his role.

— We run the whole soup to nuts. Not only are we working on the products, but everything that has to do with the drug. We have to make sure that you understand how to use the drug, how to be able to prescribe certain pieces of information, how to communicate that to the patient, he explains his role.

In front of independent journalist James O’Keefe’s OMG hidden cameras, he confirms that Johnson & Johnson was well aware that the preparation was not safe and effective.

— Do you have any idea the lack of research that was done on those products? You shouldn’t be surprised that this happened. It was pretty much the government kind of made a deal with pharmaceutical companies and kind of pressured the pharmaceutical companies, because we’re not going to say no to the government.

— I mean, none of that stuff was safe and effective. We didn’t do the typical test. The typical process, that’s why it takes so long to get a product on market, the typical process is all this clinical trial testing and stuff in a small population, Rys continues.

— This was just, let’s test it on some lab route models, analyze and see if it works and stuff like that, and just roll it to the wind and see what happens, he adds.

Kennedy halts US support for global vaccine alliance

The criticized covid vaccinations

Published 28 June 2025
– By Editorial Staff
According to Kennedy, Gavi has exhausted the public’s – and the US government’s – trust.
2 minute read

US Secretary of Health Robert F. Kennedy Jr. announced during a meeting in Brussels this week that the country is withdrawing its financial support for the global vaccine alliance Gavi.

The announcement comes as Gavi has launched a new funding round with the goal of raising at least $9 billion for the next five years.

Kennedy, who has long been highly skeptical of large-scale mass vaccination programs and experimental vaccines, sharply criticized Gavi and its collaboration with the World Health Organization (WHO) during the coronavirus crisis in a brief video address. He accused the alliance of systematically silencing “dissenting views” and ignoring health risks and safety issues related to the vaccines.

“In its zeal to promote universal vaccination, Gavi, the Vaccine Alliance has neglected the key issue of vaccine safety”, Kennedy later wrote in a post on X, and continued:

“When vaccine safety issues have come before GAVI, it has treated them not as a patient health problem, but as a public relations problem”.

Kennedy also questioned the safety of the combined vaccine against diphtheria, tetanus, and pertussis, claiming that research shows girls who received the vaccine are at higher risk of dying from other causes than unvaccinated children. He also expressed skepticism about WHO’s and Gavi’s recommendation to vaccinate pregnant women against COVID-19 – a recommendation he called “questionable”.

“I call on GAVI to re-earn the public trust and to justify the $8 billion dollars that America has provided in funding since 2001. Until that happens the United States won’t contribute more to GAVI. Business as usual is over”, he declared.

US promised one billion

According to Kennedy, Gavi must start “consider the best science available, even when that science contradicts established paradigms”.

In a statement on Thursday, Gavi claimed that the organization’s highest priority is children’s health and safety. They also stated that all decisions about which vaccines to procure are made according to recommendations from WHO’s expert group on vaccines.

Gavi is a global partnership between WHO, UNICEF, the Gates Foundation, the World Bank, and several governments, working to promote affordable mass vaccination programs in poor countries. The United States has long been one of the organization’s largest donors – and had, before Donald Trump’s re-election, promised support of $1 billion through 2030.

US removes COVID vaccine recommendation for children and pregnant women

The criticized covid vaccinations

Published 28 May 2025
– By Editorial Staff
Kennedy has long been highly critical of the way the Biden administration urged that even young children be injected with the experimental vaccines.
3 minute read

The US government has removed the experimental COVID-19 vaccines from the list of recommended vaccinations for healthy pregnant women and children.

We’re now one step closer to realizing President Trump’s promise to make America healthy again, declared Health Secretary Robert F. Kennedy Jr. when announcing the decision.

– I couldn’t be more pleased to announce that as of today the COVID vaccine for healthy children and healthy pregnant women has been removed from the CDC recommended immunization schedule, RFK said in a video posted on X yesterday.

According to analysts, the decision will most likely mean that significantly fewer children and pregnant women will be vaccinated with the heavily criticized vaccines in the future – partly because this is not recommended by the authorities – but also because many insurance companies will likely no longer cover the cost.

– Last year the Biden administration urged healthy children to get yet another COVID shot despite the lack of any clinical data to support the repeat booster strategy in children, Kennedy continued.

“Common sense and good science”

At the announcement, Kennedy was flanked by Food and Drug Administration (FDA) Commissioner Dr. Martin Makary and National Health Service Chief Dr. Jay Bhattacharya.

– It’s common sense and it’s good science, Bhattacharya said.

– There’s no evidence healthy kids need it today and most countries have stopped recommending it for children, Makary added.

Even the US Department of Health and Human Services press secretary, Vianca N. Rodriguez Feliciano, states that “HHS and the CDC remain committed to gold standard science and to ensuring the health and well-being of all Americans – especially our nation’s children”.

“A victory for all children and pregnant women”

Since the vaccines became available, the government has recommended them to almost all citizens including children and pregnant women.

Mary Holland, CEO of Children’s Health Defense (CHD) which early on urged the CDC not to recommend the vaccine for children and challenged the agency after the decision welcomes the announcement.

– Hallelujah! Holland said, adding: “These dangerous, poorly tested shots have caused injuries and death to far too many children. And many of the vaccines’ long-term side effects remain unknown. This is a major step in the right direction”.

– CHD urged the CDC not to add these dangerous vaccines to the childhood schedule. When we were ignored, we fought relentlessly to get them removed. This is a victory for all children and pregnant women.

In 2022, CHD sued the US federal Food and Drug Administration for granting emergency approval of COVID-19 vaccines for children and infants. The lawsuit alleged that the FDA abused its emergency use authorization power to push dangerous biological substances on minors. The organization appealed all the way to the US Supreme Court, which ultimately declined to hear the case.

“Emergency use authorized” for 5-year-olds

Even during the most panicked phases of the coronavirus crisis, experts agreed that children were at extremely low risk from COVID-19. Shortly after the vaccines were approved, side effects were reported, and peer-reviewed studies linked the vaccine to myocarditis and pericarditis, particularly in young people, in addition to several other health risks.

Despite this, public health authorities initially approved the vaccine for people aged 16 and older, and extended it to 12-year-olds in May 2021. The FDA then approved the vaccine for children aged 5 and older in October 2021, and for infants aged 6 months in June 2022.

However, the COVID-19 vaccine has never received full approval from the FDA for children under 12 it is still only authorized for use under emergency use authorization.

Nevertheless, the CDC added COVID vaccination to its routine vaccination schedule for children and adults in February 2023, after the agency’s advisory committee unanimously recommended it. The CDC has since continued to recommend annual booster doses for children.

The federal vaccination schedule also forms the basis for the vaccination recommendations given by most doctors, and also serves as formal guidance for state and local public health authorities that determine which vaccinations are required for school attendance. Children must usually have received all vaccines on the schedule to be considered “up to date”.

EU’s withholding of Pfizer vaccine texts ruled illegal by court

The criticized covid vaccinations

Published 15 May 2025
– By Editorial Staff
European Commission President Ursula von der Leyen and Pfizer CEO Albert Bourla had secret text message conversations in 2021.
2 minute read

The European Commission is found guilty by the European Court of Justice of withholding text messages between Ursula von der Leyen and Pfizer’s CEO in connection with the multi-billion euro purchase of COVID-19 vaccines. The Court ruled that the Commission violated transparency legislation when it refused to disclose the messages.

Now the Commission must disclose the conversations or provide a more credible explanation for why it cannot disclose them.

In spring 2021, it emerged that the President of the European Commission, Ursula von der Leyen, and Pfizer’s CEO, Albert Bourla, had private text message conversations in connection with the comprehensive COVID-19 vaccine agreement concluded between the EU and the pharmaceutical company. The agreement covered 1.8 billion doses of COVID-19 vaccine, but few details of how it was reached have been made public. For example, the price tag for each dose is still not known.

When a journalist from the New York Times requested the text message conversations between von der Leyen and Bourla, it was announced that these had been deleted. The following year, the European Court of Auditors reviewed the case and questioned why the European Commission did not disclose the text messages or other written details of the agreement. Furthermore, the Commission is said to have chosen not to share any written details of the agreement, something it has been transparent about in the past, which was of course also questioned by the Court.

The European Court of Auditors has no authority to demand more information about the text message conversations, but the New York Times chose in 2023 to file a lawsuit in the matter and this week the case was brought before the European Court of Justice. The court was asked to examine whether the European Commission had breached the law by not disclosing the conversations.

Court: “Must provide credible explanations”

The court’s decision finds that the European Commission did break the law when it refused to disclose the text message conversations between the chairman and the CEO, reports the New York Times. Under EU transparency laws, the conversations should have been shared with the newspaper.

The European Commission claimed that it did not consider the conversations important and therefore deleted them and that they cannot be retrieved. However, it never explained the extent of the search for them, which the Court considers insufficient.

The commission cannot merely state that it does not hold the requested documents but must provide credible explanations enabling the public and the court to understand why those documents cannot be found”, the Court said.

It is unclear whether the text messages have actually been deleted, but the court ruled that the European Commission must now either disclose the conversations, or at least provide a more detailed and credible explanation as to why they cannot be disclosed. In a statement, the European Commission said it would “adopt a new decision providing a more detailed explanation”.

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