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New WHO study on vaccine injuries linked to the vaccine lobby

The criticized covid vaccinations

Published 2 March 2024
– By Editorial Staff
Bill Gates has spent a considerable amount of money on various vaccine projects around the world.

The covid vaccine may be associated with an increased risk of heart muscle inflammation and blood clots in the brain. This is the conclusion of a WHO research project funded by the US Centers for Disease Control and Prevention and the globalist and vaccine lobbyist Bill Gates Foundation. At the same time, it downplays the dangers, saying that these are “rare cases”.

In a study widely circulated on social media, a “global network of researchers” reviewed data from 99 million people in eight countries and concluded that Pfizer’s and Moderna’s covid vaccines may be associated with an increased risk of inflammation of the heart muscle, while Astra Zeneca’s vaccine may lead to “rare cases” of blood clots in the brain.

The researchers also note that the vaccine has been linked to an increased risk of the neurological disease Guillain-Barré syndrome, in which the immune system attacks the peripheral nervous system. A possible link between the drugs and inflammation of the spinal cord and brain has also been discovered.

Although the researchers have identified risks with the vaccine that were not previously widely recognized, they stress that injuries are rare and say that the “few potential safety signals” that have been identified. They are also careful to point out that it is estimated that most people who receive the injections do not experience injuries or serious side effects.

– Both things can be true. They can save millions of lives, and there can be a small number of people who’ve been adversely affected, Harlan Krumholz, the study’s principal investigator and director of the Yale New Haven Hospital Center for Outcomes Research and Evaluation, said in an interview.

“Vaccine safety and efficacy”

Jacob Glanville, CEO of the biotech company Centifax, argues that the results of the study indicate that the risks of blood clots in the brain and inflammation of the heart muscle are “much higher” for those infected with covid than for those injected with the covid vaccine.

– So vaccination is still by far the safer choice, he asserts.

The high-profile study was produced by the Global COVID Vaccine Safety (GCoVS) project, which is part of the WHO Global Vaccine Data Network (GVDN) project. The project is described as “a consortium of research sites ready to conduct globally coordinated epidemiologic studies of the safety of vaccines, including COVID-19 vaccines, as they are introduced”.

“We aim to facilitate collaborative studies of vaccine safety and effectiveness using health data from diverse populations in countries around the world. With international cooperation it is now possible to have a large enough population to conduct robust analyses of rare events following vaccination”, it continues.

“Our aims are to work with vaccine safety and effectiveness experts, global health agencies, and other global non-profit health alliances to help assure the safety and risk benefit of vaccines through vaccine monitoring”, one can also read on the Global Vaccine Data Network homepage.

Gates Foundation

GVDN says it works “closely” with vaccine safety experts around the world – as well as “global health authorities and other global nonprofit health organizations”. Its work was initially made possible by seed funding from the controversial Bill & Melinda Gates Foundation, run by multi-billionaire and high-profile vaccine advocate Bill Gates.

“In April 2021, the GVDN® received significant funding from the U.S. Centers for Disease Control and Prevention for project over three years, entitled Global Covid Vaccine Safety (GCoVS). In August 2022, the U.S. Centers for Disease Control and Prevention granted additional funding to extend the GCoVS project by two years and expand the number of sites participating globally. The purpose of this project is to put in place a coordinated and harmonised post-introduction active surveillance infrastructure in diverse populations across the globe to assess the safety of COVID-19 vaccines”, the statement said.

The GVDN board is co-chaired by Steve Black, a retired professor of pediatrics who has been involved in several immunization programs, and vaccinologists Helen Petousis-Harris and Jim Buttery. The work is based at the University of Auckland, Waipapa Taumata Rau in New Zealand.

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Zuckerberg: Biden administration forced us to censor vaccine criticism

Internet censorship

Published 11 January 2025
– By Editorial Staff
Mark Zuckerberg says it was Biden's team that forced Facebook to censor vaccine criticism.

In an interview with podcaster Joe Rogan, Meta CEO Mark Zuckerberg says it was the Biden administration that forced the company’s platforms to censor posts criticizing the experimental COVID-19 vaccines.

The conversation covered several topics, but one that stood out was when Zuckerberg talked about government censorship and how the outgoing administration forced the tech company to weed out uncomfortable opinions – even if they were completely true.

– This hit the most extreme. I’d say it was during the Biden Administration when they were trying to roll out the vaccine programme. Now I’m generally pretty pro rolling out vaccines, I think on balance the vaccines are more positive than negative but I think that while they’re trying to push that program they also tried to censor anyone who was arguing against it.

– They pushed us super hard to take down things that were honestly true. I mean, they basically pushed us and said, ‘You know anything that says that vaccines might have side effects, you need to take down’ , the billionaire explained in the interview, claiming he opposed this demand.

According to Zuckerberg, representatives of the Biden administration contacted him personally and demanded that posts highlighting the side effects of the mRNA vaccine be deleted.

That’s ridiculous

Referring to the investigation, and the committee set up to look into the Biden administration’s censorship, Mark Zuckerberg went on to say that government representatives called and yelled at Meta’s team, demanding that various posts, even of a humorous nature, be deleted immediately.

– It just got to this point where we were like, no, we’re not gonna take down true things. That’s ridiculous… We’re not going to take down humor and satire.

According to Zuckerberg, his alleged refusal to comply with the Biden administration’s censorship demands also led the government to begin attacking his company through various pronouncements and government investigations.

– It was brutal, he claims.

With the departure of the Biden administration and the arrival of the Trump administration, the Facebook founder says it is high time to “restore freedom of expression” on platforms that were previously subject to widespread and arbitrary censorship, and where dissent was often effectively banned.

– We will go back to our roots, they say.

“Criminal censorship”

Not everyone finds Zuckerberg’s claims particularly credible, however. For example, author David Icke, an early critic of mass vaccination programs, points out that he was censored and suspended from Facebook back in 2020 when Donald Trump was president.

They are all at it – letting Zuckerberg’s criminal censorship be whitewashed to bring him into the MAGA fold while Biden takes the blame”, he writes.

Swedish MP pushes for accountability on mRNA vaccine risks

The criticized covid vaccinations

Published 30 November 2024
– By Editorial Staff
Elsa Widding calls on the government to stop the use of mRNA products until their risks are properly assessed.

In an interpellation debate, Elsa Widding asks whether Social Affairs Minister Jacob Forssmed (KD) will investigate the strong suspicions that the mRNA vaccine has a very harmful effect on the human genome and stop all use of the experimental vaccines until such an investigation is completed.

However, Forssmed is not interested in thoroughly investigating the harmful effects of the vaccine, claiming that the controls are already “rigorous and comprehensive”. Nor does he seem to want to take any personal responsibility for the consequences of mRNA technology.

Independent member of the Swedish Parliament Elsa Widding, addressed an interpellation to Minister of Social Affairs Jacob Forssmed in light of the experimental mRNA vaccine during the COVID crisis and the dangers and negative health effects suspected to be linked to the vaccine.

Widding refers to a wide range of experts and points out how there is a lot of evidence to suggest that mRNA vaccines can, among other things, be contaminated with bacterial DNA and thus carry a risk of very serious damage to human health.

– This is because synthetic foreign DNA is encapsulated in lipid nanoparticles, which can then integrate into human cells, leading to genomic instability, cancer, immune system disorders and adverse hereditary effects.

“Will the Minister take responsibility?”

She therefore asks Forssmed whether he will set up an independent investigation into the strong suspicions that the vaccine affects the human genome and whether he will stop all use of products based on mRNA technology until the above investigation is completed.

– If the Minister chooses not to stop the use of mRNA technology in Sweden, will the Minister take full responsibility for the consequences? she asks.

However, Forssmed does not seem to be prepared to take any personal responsibility at all and he calls the process of checking the vaccine “rigorous and comprehensive“.

I have good faith in the process related to the control and monitoring of medicines and vaccines, and I believe it is important that those who are deemed to be at risk of serious illness from COVID-19 can continue to receive the protection offered by the vaccine, he says.

“Dark shadow hangs over the authorities”

Widding soon becomes visibly frustrated in the debate that the Minister for Social Affairs does not seem to be interested in answering her questions at all and also seems to misunderstand what she is trying to get across.

– So the question is not whether the contaminating foreign DNA integrates into the DNA of human cells, but how often this happens and how serious the effects are.

– The genetic risks to humans and their offspring are unknown. That is why further scientific studies to determine these risks are urgently needed. Similarly, the government should investigate, for example, excess mortality, which remains very high in the Western world. If you look at the years 2020, 2021 and 2022, you can see that it was highest in 2021, when vaccination started, and still very high in 2022. Why is this not being investigated? Is there a link with the vaccines or not? she continues.

The independent MP argues that the monitoring of mRNA vaccines is not at all as “rigorous and comprehensive” as Forssmed claims – instead, many rules and best practices for clinical trials were violated during the COVID crisis.

– Someone – the manufacturer – has been sloppy in the manufacturing process of the modified mRNA vaccine, and the authorities have let them get away with it. I would therefore say that a very dark shadow hangs over the same authorities that the Minister is defending. Safe and effective vaccines cannot be produced as long as regulators do not act in the public interest.

Not preventing the spread of infection

Forssmed continues to avoid Widdings’ questions and instead declares that he is “confident that the vaccines used against COVID-19 are of good quality and that they are safe and effective against serious illness and death“.

It is problematic that this type of non-scientific claims are spread, and it is of course not relevant to stop vaccinations with safe, effective and approved vaccines, the Minister continued.

Ms. Widdings’ irritation at the minister’s dodging of her questions is growing, and she also points out that the authorities may not have as much credibility on the vaccine issue as they would like to claim.


Translation: Head-in-the-sand behavior from Social Affairs Minister Forssmed.

– First, COVID-19 vaccines have never even been tested for their ability to block virus transmission and thus do not protect against the spread of infection. European regulators, as well as governments and state bodies, misled people to get them to accept these products. Hasn’t this affected the credibility of the authorities? Here I would like to remind the Council of State of the text of the Nuremberg Code, that is, the prohibition of subjecting people to experiments and of forcing, pressuring or persuading people to participate in medical experiments against their will.

– Second, the COVID-19 vaccines resulted in an unprecedented level of reported adverse events, including deaths. Moreover, analysis of public data shows that it was completely random which batch of vaccine a person received and thus also random which side effects the person suffered after the shot. Those who were unlucky enough to receive a shot from a really bad batch of modified mRNA vaccine had a 1 in 20 risk of becoming very seriously ill or dying. Others, who received their vaccine from the most favorable batch, had a minimal risk of illness or death.

– Third, analysis by several independent scientists now shows that Pfizer’s and Moderna’s products were contaminated with varying and uniquely high levels of residual DNA. It is this contamination that is at the heart of today’s debate…How can a vaccine be considered safe and effective when hardly anyone even knows what it contains?

“Affects the brain, heart and lungs”

Widding also highlights how the pressure for Swedes to take the experimental vaccines was enormous and how people were fooled into thinking they were preventing the spread of infection if they were vaccinated even though this was not the case.

She highlights how modified mRNA vaccines against COVID-19 pose health risks that were not adequately studied before the vaccines were granted emergency approval and began to be injected into the world’s populations.

– The lipid nanoparticles do not stop at the injection site but reach the bloodstream and thus several organs. If cells in the blood vessels absorb these particles, they will cause vascular damage and blood clots, leading to an increased risk of stroke, heart attack and other acute vascular diseases. The Minister should know this if he has read the data from Pfizer. All these conditions are well documented in the medical literature and in national adverse event reporting systems. Full stop. Similarly, lipid nanoparticles can affect organs such as the brain, heart, lungs, kidneys, etc.

Vaccine manufacturers must be scrutinized

– While these risks apply to all mRNA vaccine technology, the potentially serious health risks due to the contamination with bacterial DNA we are talking about today also need to be addressed. The development of safe and effective vaccines depends on transparent and reliable oversight of vaccine manufacturers. Positive change starts with the recognition of errors, and this process must start immediately before more lives are lost in a careless and unnecessary way. A huge responsibility rests here on the shoulders of the Prime Minister, she concluded.

Despite repeated calls and direct questions, Forssmed continues to refuse to answer them, instead repeating mantras such as “we need to continue vaccinating” and that “it is important that people in risk groups receive vaccines“.

It is important that we continue to stand up for science and the thousands of researchers who say that this is good and important and protects against severe disease and death, he says.

Von der Leyen’s ‘Pfizergate’ taken to the European Court of Justice

The criticized covid vaccinations

Published 12 October 2024
– By Editorial Staff
Ursula von der Leyen and Albert Bourla had private SMS conversations about covid vaccine contracts in 2021.

The Court of Justice of the European Union will now consider whether the European Commission’s reasons for refusing the New York Times access to text messages between Pfizer’s CEO and the EU president are valid. The case is due to start in November.

It was in April 2021 that the New York Times reported that the president of the European Commission, Ursula von der Leyen, and the CEO of Pfizer, Albert Bourla, had private text message conversations about the huge covid-19 vaccine deal, which was concluded in May of that year. The newspaper requested these text messages from the Commission, but von der Leyen claimed they had been deleted.

The European Union’s Court of Auditors audited the covid vaccine deal and published a report in September 2022 that, among other things, questioned the Commission’s reluctance to disclose von der Leyen’s personal role in the deal.

The New York Times then decided to sue the European Commission on the grounds that these text messages between the president and the CEO should be covered by freedom of information laws, as the conversations concerned an agreement within the EU.

– The public continues to be denied information about the terms of one of the biggest procurement contracts in the history of the EU, said Nicole Taylor, spokesperson for the newspaper, according to Politico.

Von der Leyen was “personally involved”

On 15 November the case will be heard by the EU’s highest court, the CJEU, reports the Financial Times. It will decide whether the Commission’s reasons for refusing access to the New York Times are valid, and thus whether SMS messages should be considered documents that must be stored and remain accessible to citizens.

Among other things, the Court is expected to ask the Commission’s legal representatives to explain whether the text messages ever existed and, if so, why they were not recorded. They are also expected to be asked whether they deleted these text messages and, if so, for what reasons.

According to the New York Times, both Bourla and von der Leyen have admitted to private text messages about the deal, with the president also saying she was “personally involved” in the deal.

In the run-up to the European elections last summer, the European Court of Justice ruled in a separate case concerning the covid vaccine deal that the Commission had illegally withheld certain details, AP News reported. The case involved a group of MEPs who took legal action after the Commission refused to give them full access to the covid vaccine deal. Despite the criticism, which was mainly directed at Ursula von der Leyen, she was re-elected as president of the European Commission.

Despite this unresolved issue, the European Commission has continued to sign new contracts with the pharmaceutical giant. Last year, for example, it bought an additional 2.4 billion doses of Pfizer’s covid vaccine.

Moderna offered children money to test covid vaccine

The criticized covid vaccinations

Published 9 October 2024
– By Editorial Staff

Moderna representatives allegedly offered children and young people money to take part in covid-19 vaccine trials via Whatsapp. UK regulators criticised them for bringing “discredit upon the pharmaceutical industry”.

Children aged between 12 and 18 were offered £1,500 (€1,790) to take part in the NextCove study, which is testing booster doses of Moderna’s covid-19 vaccine in children and adolescents. The children and adolescents were invited by a paediatrician via the Whatsapp app, reports The Telegraph.

After a research ethics committee raised concerns about the amount of money involved, Moderna reduced the reimbursement to £185 (€220), but at least one trial centre will continue to offer the original, higher amount. According to the UK Medicines for Human Use (Clinical Trials) Regulations, however, it is strictly prohibited to offer incentives or financial compensation to children or their parents.

The UK’s Prescription Medicines Code of Practice Authority (PMCPA) has ruled that the company’s behaviour amounted to an “inappropriate financial inducement”, and also states that the company has brought “discredit upon the pharmaceutical industry”.

“The panel considered that the unique circumstances of the Covid-19 pandemic, and the particular circumstances of this trial, which involved the recruitment of children, meant that Moderna should have been especially cautious. On balance, the panel considered that this brought discredit upon and reduced confidence in the pharmaceutical industry”, the PMCA said in a statement on the case.

Moderna must give a written undertaking to “cease forthwith” with the proceedings. The company was also ordered to pay £14,000, or almost (€16,700). In 2023, the company had a revenue of around 70 billion SEK (€6 billion).