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I, along with six colleagues, wrote a letter to the European Medicines Agency (EMA) expressing concerns about the COVID vaccines. The EMA responded, revealing shocking facts. They clarified that the vaccines were only approved for individual immunization, not for controlling or preventing infections. The EMA emphasized the lack of data on contagiousness and even stated that repeated exposure to the virus could increase the risk of infection in vaccinated individuals. The government's campaigns promoting vaccination to protect others were unauthorized and based on misinformation. The EMA also highlighted the importance of carefully considering safety information before administering vaccines. The government's failure to report vaccine side effects within the first 14 days was not only fraudulent but also endangered lives. The vaccination campaign should be halted as it does not meet EMA standards. The government and supporting political parties should be held accountable for their lies and deception.

A group of European Parliament members wrote a letter to the European Medicines Agency (EMA) expressing concerns about the COVID-19 vaccines. The EMA responded, stating that the vaccines were only approved for individual immunization and not for controlling or preventing infections. They also admitted a lack of data on vaccine effectiveness against infections. The government's campaign to vaccinate for the sake of others was based on misinformation. Furthermore, the EMA emphasized the need to carefully consider safety information before administering vaccines. The mass vaccination campaign should be halted as it does not meet the EMA's requirements and puts people's health at risk. The government and supporting political parties should be held accountable for their lies and deception.

A group of European Parliament members wrote a letter to the European Medicines Agency (EMA) expressing concerns about the COVID-19 vaccines. The EMA responded, stating that the vaccines were only approved for individual immunization, not for controlling or preventing infections. They also emphasized the lack of data on preventing infections and even mentioned that exposure to the virus could increase the risk of infection, even in vaccinated individuals. The EMA highlighted the importance of carefully considering safety information before administering vaccines. The government's vaccination campaigns were deemed unauthorized and based on misinformation. The EMA's information undermines the vaccination policies of the Dutch government, and they should be held accountable for their actions.

The video discusses the different processes used to create COVID-19 vaccines, specifically the mRNA vaccines from Moderna and Pfizer. The first process, called Process 1, involved a synthetic PCR method and was tested on 40,000 people. However, a second process, tested on only 252 people, was used to produce vaccines for billions of people. This second process involved using a complementary DNA sequence to make the mRNA. It is revealed that this process was not properly tested and resulted in bacterial plasmid DNA contamination in the vaccines. The presence of this contamination raises concerns about potential long-term effects, such as autoimmune diseases and cancers. The video criticizes the fact that contaminated products are still being distributed despite the risks involved.

Last month, a group of European Parliament members, including myself, wrote a letter to the European Medicines Agency (EMA) expressing concerns about the COVID-19 vaccines. The EMA's response revealed shocking facts. They admitted that the vaccines were only approved for individual immunization and not for controlling or preventing infections. Furthermore, there is a lack of data supporting the vaccines' effectiveness in preventing infections. In fact, the EMA stated that repeated exposure to the virus increases the risk of infection even in vaccinated individuals. The government's campaigns promoting vaccination to protect others were unauthorized and based on misinformation. The EMA also emphasized the need to carefully consider safety information before administering vaccines. The mass vaccination efforts were in direct contradiction to the approved use of the vaccines. The government and supporting political parties should be held accountable for their lies and deception. The vaccination campaign needs to be halted as it is not safe and does not meet EMA requirements.

The speaker criticizes a report for omitting important information discussed in the committee. They highlight that contracts were not fully disclosed and mention a scandal involving text messages between Ursula von der Leyen and Albert Bourla. They question the safety and effectiveness of the injections, citing a statement from a Pfizer representative. The speaker argues that information about the SARS CoV-two virus was known prior to the report's claim. They also dispute the claim that vaccines saved 250,000 lives, pointing out the high mortality rates in highly vaccinated countries. The abusive use of the Digital Green Certificate and the violation of individuals' rights to consent are also mentioned. The speaker concludes that this report highlights a disconnect between EU institutions and its citizens.

In this video, several topics are covered, including the influence of BlackRock on major pharmaceutical and processed food companies, concerns about the COVID-19 pandemic and mRNA vaccines, and the threats faced by a New Zealand whistleblower and journalist. The speakers express skepticism towards the government, question the science behind the vaccines, and raise concerns about the intentions of big pharma. They emphasize the need for transparency, accountability, and the protection of individual rights.

Willem Engel, a pharmaceutical scientist and human rights activist, discusses the concerns and safety issues surrounding COVID vaccines. He criticizes the spread of misinformation by governments and the lack of accurate registration of vaccine risks. He questions the validity of informed consent when crucial information is not shared with the public. Another speaker highlights the patterns of adverse reactions in different vaccine batches, suggesting that informed consent was impossible due to the unknown risks associated with each batch. The statistician presents data showing three distinct patterns of adverse reactions in different vaccine batches, indicating a concerning safety signal. The speakers call for the withdrawal of vaccine marketing authorizations and accountability for the alleged mishandling of the vaccination campaign.

John Loughlin, director of FVD International, discusses a letter written by Marcel de Graaf, Joachim Koos, and other members of the European Parliament to the European Medical Agency. The letter raises concerns about the procedures followed and changes made in the approval process for COVID vaccines. It also highlights the alleged harmful nature of the vaccines and the confusion between testing batches and those used on people. The speakers argue that the vaccines are not effective and that the approval process has been corrupted. They discuss the dangers of the vaccines, including myocarditis and heart disease, and question the legality and safety of genetically modified organisms used in the vaccines. The speakers also mention allegations of corruption and suppression of text messages by Ursula von der Leyen.

Last month, Joachim Küs and six other colleagues from the European Parliament wrote a letter to the European Medicines Agency (EMA) regarding concerns about the vaccines. The EMA responded, stating that the vaccines were only authorized for individual immunization and not for infection control, prevention, or reduction. In fact, the EMA highlighted a lack of data on contagion and stated that repeated exposure to the virus could increase the risk of infection even in vaccinated individuals. The massive vaccination campaigns aimed at protecting others were not authorized and lacked factual basis. The EMA emphasized that vaccinations were solely for the protection of the vaccinated individual, and safety information should be carefully considered before administering or recommending a vaccine. The government's vaccination policies disregarded this information, putting lives at risk. Vaccination campaigns should be halted immediately, and those responsible for the lies and deception held accountable.

Last month, Joachim Küs and six other colleagues from the European Parliament wrote a letter to the European Medicines Agency (EMA) regarding concerns about the vaccines. The EMA responded, stating that the vaccines were only authorized for individual immunization and not for infection control, prevention, or reduction. In fact, the EMA highlighted a lack of data on the vaccines' ability to prevent infections. The EMA also mentioned that repeated exposure to the virus could increase the risk of infection even in vaccinated individuals. The massive vaccination campaigns aimed at protecting others were not authorized and lacked factual basis. The EMA emphasized that vaccinations were solely for the protection of the vaccinated individual, and safety information should be carefully considered before administering vaccines. The government's vaccination policies and failure to report side effects were deemed dangerous and fraudulent. Vaccination campaigns should be halted immediately.

The speakers in the video discuss various red flags and concerns regarding the COVID-19 vaccines. They highlight the importance of accurate information and informed consent for individuals deciding whether to get vaccinated. They criticize government policies and media campaigns for downplaying the risks and side effects of the vaccines. The speakers also raise concerns about the registration of adverse events and the existence of a closed database containing more serious side effects. They emphasize the need for transparency, accountability, and further investigation into the safety and long-term effects of the vaccines.

I am Marcel de Graaf, Member of the European Parliament for Forum for Democracy. I recently sent a letter to the European Medicines Agency (EMA) regarding the approval of medications in the European market, specifically questioning the COVID-19 vaccines. We have received a response that clarifies many issues. This response is highly critical of the vaccination policy in the Netherlands. I will provide more details in a press conference tomorrow at 3 PM via a livestream from Strasbourg. The EMA's response confirms that Forum for Democracy's criticism of the vaccination policy is justified.

Marcel de Graaf, Willem Engel, and others discuss the safety issues and lack of informed consent surrounding COVID vaccines in a press conference. They highlight the existence of different batches of vaccines with varying risks, the failure of the European Medicines Agency (EMA) to properly inform the public, and the potential long-term side effects. They also question the classification of the vaccines as vaccines rather than gene therapy and raise concerns about the manipulation of data and the lack of transparency. The speakers call for the withdrawal of market authorizations and accountability for those responsible.

In this video, the speaker discusses the adverse effects of COVID-19 vaccines and criticizes the lack of transparency and accountability in the vaccination process. They highlight the rise in serious health emergencies, the neglect of natural immunity, and the higher rate of adverse events compared to other vaccines. The speaker calls for the release of data on vaccine dosage, dates, and deaths, and expresses concern over the public's diminishing trust in health services, media, and politics. They also mention their personal sacrifices for speaking out against the vaccines and emphasize the need to challenge the powerful interests involved.

I am one of the scientists involved in a study on the safety and dependency of vaccine batches. We found three types of side effects: mild, severe, and even death. These adverse effects were present in the initial batches, which may have been changed during production or transportation. Patients were not informed of the risks and some received poor-quality batches. The Vice President of Pfizer admitted to building the plane while flying, and we have shown that one wing has fallen off. There is a safety issue that the European Medicines Agency (EMA) and national institutions should have addressed and informed the public about. Our study also suggests a potential link between certain cancers and different vaccine batches. We have observed increased mortality rates in European countries since May 21st. The EMA should have reacted to these findings and halted vaccinations or at least withdrawn the problematic batches. As a concerned citizen and doctor, I expected more action from the EMA. Thank you.

In this video, the speaker discusses the presence of DNA fragments in COVID mRNA vaccines. They mention that while it has been proven in the laboratory, it hasn't been solidly proven in real-life human beings. The speaker criticizes certain individuals for not responding to their communications over the past two years. They also claim that the vaccine has caused a high number of deaths and injuries. The speaker suggests that people should be aware of the corruption in healthcare systems and recommends using products from a wellness company. The video concludes with a promotion for the wellness company's medical emergency kit.

Last month, I, along with six colleagues from the European Parliament, wrote a letter to the European Medicines Agency (EMA) expressing concerns about the COVID vaccines. The EMA's response revealed shocking facts. They admitted that the vaccines were only approved for individual immunization, not for controlling or preventing infections. The EMA emphasized the lack of data on the vaccines' ability to prevent transmission. In fact, repeated exposure to the virus could increase the risk of infection even in vaccinated individuals. The government's campaigns promoting vaccination to protect others were unauthorized and based on misinformation. The EMA also stated that vaccinations were solely for the protection of the vaccinated individual, and each case should be carefully evaluated for safety before administering the vaccine. The government's vaccination policy disregarded reporting of side effects within the first two weeks after vaccination, falsely attributing any complaints to the virus. This information exposes the flaws in the vaccination strategy and calls for an immediate halt to the campaign.

The speaker discusses their observations and analysis of the COVID-19 pandemic. They claim that the World Health Organization (WHO) has played an adverse role in both the virus's origins and the vaccine rollout. They believe that the WHO is part of a complex syndicate that includes various organizations and foundations. The speaker criticizes the WHO for not supporting early treatment protocols and claims that the vaccines have caused significant harm, including cardiovascular disease, neurologic issues, blood clots, and immunologic abnormalities. They argue that the vaccines should be removed from the market and urge the European Medicine Agency to take action. They also suggest that major stakeholders should withdraw from the WHO.

Last month, Joachim Küs and six other colleagues from the European Parliament wrote a letter to the European Medicines Agency (EMA) regarding concerns about the arrival of vaccines. The EMA responded, stating that the vaccines were only authorized for individual immunization, not for infection control, prevention, or reduction. The EMA also highlighted a lack of data on contagion and stated that repeated exposure to the virus could increase the risk of infection even in vaccinated individuals. The government's massive vaccination campaigns, aimed at protecting others, were not authorized and lacked factual basis. The EMA emphasized the importance of carefully considering safety information before administering vaccinations. The government's policy of not reporting complaints within the first 14 days of vaccination was seen as deliberate endangerment of human life. The speaker called for an end to vaccination campaigns and accountability for the government's lies and deception.

In this video, various experts discuss the risks and concerns surrounding experimental vaccines, particularly in relation to COVID-19. Professor Christian Péronne criticizes the rushed development and lack of long-term safety data for these vaccines, questioning their efficacy and safety. He highlights the importance of proper placebo-controlled studies and the need for further research on vaccine safety. Another speaker discusses the effectiveness and limitations of vaccines, emphasizing the importance of reading vaccine notices carefully and considering various factors in treatment decisions. They express concerns about the influence of pharmaceutical companies on medical research and advocate for transparency. Additionally, the impact of the HPV vaccine on reducing precancerous lesions is discussed, along with concerns about the influence of pharmaceutical companies on authorities and the lack of independent studies. The speaker calls for a reform of the World Health Organization (WHO) and expresses skepticism about the COVID-19 pandemic and vaccine. They emphasize the importance of vigilance against the suppression of freedoms and criticize the influence of big corporations.

Today's press conference featured Marcel De Graff, a European Parliament member, along with Joachim Kus, Evi Becquehmanish, and Max Schmeling. They discussed the shocking response from the European Medicines Agency (EMA) regarding the authorization of COVID-19 vaccines. The EMA explicitly stated that the vaccines were only authorized for individual immunization and not for infection control or prevention. This contradicts the government's messaging and raises concerns about the safety of the vaccines. The speakers also highlighted the lack of proper reporting of side effects and the potential risks associated with different vaccine batches. They called for an immediate halt to vaccination campaigns and accountability for the government's misleading information.

In this video, John Loughlin interviews Marcel de Graaf, Joachim Koos, and Willem Engel about their letter to the European Medical Agency (EMA) regarding the withdrawal of COVID vaccines. They discuss various arguments against the vaccines, including procedural violations, alleged confusion between test batches and actual batches, and the harmful nature of the vaccines. They highlight the dangers of the vaccines, such as myocarditis and pericarditis, and the potential corruption and illegality surrounding their approval. They also mention the suppression of text messages by Ursula von der Leyen and the erosion of sovereignty by the European Union. The speakers express their concerns and call for action against the vaccines.

I, along with six colleagues, wrote a letter to the European Medicines Agency (EMA) expressing concerns about the COVID vaccines. The EMA's response revealed shocking facts. They admitted that the vaccines were only approved for individual immunization, not for controlling or preventing infections. The EMA emphasized the lack of data on contagiousness and stated that repeated exposure to the virus could increase the risk of infection, even for the unvaccinated. The government's campaigns promoting vaccination to protect others were unauthorized and based on false information. The EMA also highlighted the importance of carefully considering safety information before administering vaccines. The mass vaccination efforts were in direct contradiction to the approved use of the vaccines. The EMA expected reports of side effects, but the government failed to report them, endangering lives. The vaccination campaign should be halted immediately.

Willem Engel, a human rights activist, and other speakers discuss the safety issues and lack of informed consent surrounding COVID vaccines. They highlight the problem of adverse events not being properly registered within the first 14 days after vaccination, leading to a false sense of security. They also raise concerns about the classification of mRNA injections as vaccines and the potential long-term side effects. The speakers present data showing different patterns of adverse reactions in different vaccine batches, indicating a lack of consistency and informed consent. They criticize the European Medicines Agency (EMA) for not taking appropriate action and call for the withdrawal of market authorizations.