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Health authorities and the media have been accused of misleading the public about the safety of COVID injections, with evidence suggesting they concealed adverse event data. Recent emails from Australia’s Therapeutic Goods Administration (TGA) reveal that officials acknowledged the potential for DNA fragments from mRNA vaccines to integrate into human genomes, contradicting their public statements. Despite this, the TGA focused on dispelling public fears rather than investigating risks. Concerns have been raised about the lack of testing for DNA integration and the overall safety of the vaccines. Senator Gerard Renick criticized the TGA for its poor quality assurance and lack of accountability, highlighting the need for greater scrutiny of vaccine safety and the political failures that allowed these issues to persist. The situation reflects broader frustrations with government transparency and public health decisions in Australia.

Australia's healthcare system, supported by dedicated workers, is facing unprecedented challenges, including rising sickness levels among healthcare professionals. Concerns have been raised regarding synthetic DNA contamination in Pfizer and Moderna COVID-19 vaccines, with findings indicating contamination levels far exceeding safety limits. A report co-authored by 52 scientists highlights the potential risks, including cancer mutations from minimal contamination. The Therapeutic Goods Administration (TGA) has been criticized for dismissing these concerns without proper investigation, using inadequate testing methods. The Port Hedland Council has called for a suspension of these vaccines following alarming cancer trends in their community. Urgent action is needed to ensure the safety of all Australians, invoking the precautionary principle until independent testing can confirm or dispel these contamination claims. Transparency and accountability are essential to protect public health.

The Pfizer and Moderna vaccines contain fragments of DNA, which can integrate into the genomic DNA of cells and become a permanent part of the cell. This poses a potential risk of autoimmune attacks and future cancer. The DNA contamination occurred during the production process, where a plasmid vector was used to scale up the production of the RNA template. The regulatory threshold for DNA in vaccines is outdated and not suitable for this new type of vaccine. The speaker believes that DNA sequencing should be done on vaccinated individuals' stem cells to determine if this theoretical risk has occurred. Informed consent is necessary, and the lack of transparency regarding the DNA contamination is concerning.

This is not conspiracy theory. This has been published in the BMJ by Retzaf Levy, and they go through this process: one where they ran these vaccines in the trial and how they changed that when they decided to go and inject the rest of the world. This is traditionally a mortal sin in vaccine manufacturing or in any sort of biologic manufacturing. The process is the product. You change the process, you have to go through trials again. And the EMA even asked them to do that, although they failed to. They asked for another trial of 250 people once they changed the process and that data was never delivered. So this bait and switch is very important for you to understand why the trial data is of absolute zero consequence to what we're actually seeing in the field. Those numbers are a caricature of what they're actually doing with these injections. They know something. Pfizer very early on they had the data on this from their trial, they knew this was going to happen and they quickly went out and acquired cancer companies. They put $43,000,000,000 into the acquisition of C Gen and they put $2,260,000,000 to acquire Trillium Therapeutics. Trillium was focused on blood cancers that have a CD one forty seven marker on them. Okay? That is one of the markers that is known to be involved in COVID. So, they have a very interesting window on those malignancies and, they're buying up the cancer companies that are probably gonna play the biggest role in benefiting from the mess that they've created. So, in summary, the Pfizer vaccines on the market are not the same formulation as what was tested in the clinical trials. This is a big bait and switch and it's a fraud. So you can't believe anything they're saying about the vaccine efficiency, which we have seen even those numbers decay over time. This is probably why. They're not really what they trialed. They gave you something different. There is significant DNA contamination that's found. Like, 10 out of 11 studies have found this, and the ones that haven't found it have some financial conflicts. So, I think the consensus is out. 10 out of 10 out of 10 of the real studies, are finding this. Several are through peer review, which have not been easy to get through peer review. The peer review journals do not like these papers. They get beat around in peer review for months to years, but they're making their way out now. There is also significant DNA contamination now found in five peer reviewed studies that were not looking at this. They were looking at people's blood and tissue and it was accidentally in there. Other people had to go sleuth it out. We've got cancer on the rise and there's several papers that report cancer post vaccination. Like, right at the site of injection, they'll see neoplasms. Alright? There is there's something going on here. This can't be ignored saying it's a coincidence anymore. Now this is these are liability free and they're often mandated. Okay? This may be the largest carcinogenic hit ever to the human population. And we have these on childhood schedules. We're giving these to pregnant women. This has gone absolutely off the rails.

I urge the British, Australian, New Zealand, Canadian, and US governments to recognize the global health crisis linked to the mRNA vaccine platform, which has been used for COVID-19, RSV, flu, and tetanus. During the pandemic, we were constantly updated on COVID cases, yet now we face a significant health crisis affecting potentially hundreds of millions due to this mRNA technology. While it is known to be cost-effective and profitable, it is also causing injuries to millions, with potential generational effects. Governments must acknowledge this serious issue, as ignoring it raises concerns.

Mr. Kevin McKernan, a former leader at the Human Genome Project, discussed DNA contamination in Pfizer and Moderna vaccines. He highlighted the risks of insertional mutagenesis and integration into the genome, contradicting regulators' claims of little consequence. The DNA, found in lipid nanoparticles, can enter cells and potentially contribute to cancer. McKernan emphasized the inadequacy of current monitoring methods and called for a review of regulatory practices. The presence of DNA in these vaccines challenges existing safety standards and raises concerns about long-term effects.

Thank you, Senator Johnson. I want to address the DNA contamination found in Pfizer and Moderna mRNA vaccines, which has been confirmed by multiple labs and acknowledged by regulatory agencies like the FDA and EMA. They downplay the significance of this contamination, claiming it has no functional consequences, which is misleading. DNA contamination can lead to insertional mutagenesis, as noted in Moderna's patents. The contamination levels vary significantly between lots, and current measurement methods allow for selective reporting. We have evidence that this DNA can integrate into the genome, raising concerns about genotoxicity, especially given the rise in cancer drug sales since the vaccine rollout. Regulatory practices need to be reviewed, particularly the PDUFA Act, which allows regulators to accept funding from the companies they oversee, creating conflicts of interest. Informed consent processes have not addressed this contamination issue, yet mandates persist based on flawed regulatory guidance. Thank you.

Many labs, including Medicinal Genomics, found DNA contamination in Pfizer and Moderna mRNA vaccines. Regulators like the FDA and EMA admitted to this, but downplayed its significance. The SP 40 sequences omitted by Pfizer are crucial. DNA contamination can cause insertional mutagenesis, as stated in Moderna's patents. Regulatory agencies were deceived and failed to properly address the issue. This poses a serious risk that cannot be ignored.

The speaker claims that this is not conspiracy theory and cites a BMJ publication by Retzaf Levy, which describes a process in vaccine development: vaccines were trialed under one formulation, but when the decision was made to deploy them globally, the process was changed and the product injected to the rest of the world. The speaker asserts that changing the process requires new trials, yet the EMA asked for an additional trial of 250 people after the process change, and that data was never delivered. This is described as a “bait and switch,” asserted as crucial for understanding why trial data is of zero consequence to what’s seen in the field, implying that real-world outcomes do not match trial data and that the numbers from trials are a caricature of field performance. The speaker claims Pfizer had early data indicating what would happen and acted on that by acquiring cancer companies: $43,000,000,000 into the acquisition of C Gen and $2,260,000,000 to acquire Trillium Therapeutics. Trillium is described as focused on blood cancers with the CD147 marker (CD Adaptor 147) on them, a marker claimed to be known to be involved in COVID. The implication is that Pfizer is building an investment portfolio in cancer companies that would benefit from the consequences the speaker alleges they caused. In summary, the vaccines on the market are said to be not the same formulation as what was tested in clinical trials, labeling this a “bait and switch” and a fraud, and asserting that vaccine effectiveness numbers are not reliable because the products differ from trial formulations and because those numbers decay over time. The speaker alleges significant DNA contamination, stating that 10 out of 11 studies have found this, with the remaining studies allegedly constrained by financial conflicts. The claim is that consensus among real studies supports DNA contamination, with several studies through peer review, which the speaker notes is difficult for those papers to pass through peer review. It is claimed that five peer-reviewed studies not originally examining contamination found DNA in blood and tissue upon sleuthing. The speaker asserts that cancer is on the rise and that several papers report cancer post-vaccination, including neoplasms at the site of injection. The claim is that this situation cannot be dismissed as coincidence and is described as “liability free” and often mandated. The speaker posits that this may be the largest carcinogenic hit to the human population, with vaccines on childhood schedules and given to pregnant women, stating that “this has gone absolutely off the rails.”

The speaker discusses DNA contamination found in Pfizer and Moderna mRNA vaccines, highlighting regulatory agencies' failure to address the issue. They mention potential risks of DNA integration and cancer development, urging for a review of regulatory practices. Concerns are raised about DNA levels exceeding limits, potential cell integration, and long-term presence in the body. The speaker emphasizes the need for better monitoring tools and the unique nature of DNA contamination in these vaccines.

A significant debate took place in Port Hedland on November 29, 2024, addressing concerns over the Australian government's handling of COVID-19 vaccine safety. Key speaker Professor Ian Breithope highlighted alarming findings of synthetic DNA contamination in Pfizer and Moderna vaccines, which he claimed could lead to serious health issues, including cancers and autoimmune diseases. He criticized health authorities for not monitoring cancer trends post-vaccination and proposed a five-point plan to address the crisis, including monitoring cancer trends and halting contaminated vaccine distribution. Breithope emphasized the need for transparency and accountability in public health, urging that the health of future generations depends on today's actions. He concluded with a call for prioritizing human life over profits and politics.

Pfizer was criticized for marketing practices, and there are concerns about excess deaths in Australia possibly linked to the vaccine rollout. The vaccines may have systemic harm due to spike protein use. Dr. Tindall warns of potential harm to the immune system and increased cancer risk from disrupting DNA. There are suspicions of hidden cancer-linked DNA in vaccines. A study in Japan suggests a link between vaccines and increased cancer rates. The speaker urges an inquiry into vaccine safety and efficacy and calls for the government to suspend the vaccine rollout.

The Port Hedland Council in Australia has voted to suspend the Moderna and Pfizer COVID vaccines due to concerns over synthetic DNA contamination. They found levels of residual DNA in the vaccines up to 145 times above legal limits, raising fears of health risks such as cancer and immune disruption. The council plans to inform all local councils in Australia and health practitioners about these findings. This follows independent testing and pressure from federal MP Russell Broadbent, who has sought government accountability. The council aims to inspire other local governments to demand proof of vaccine safety from federal authorities, emphasizing the need for transparency and accountability regarding COVID-19 vaccinations.

I'm Philippe Boucalt, a cancer genomics researcher at the University of South Carolina. I've sequenced the DNA in the Pfizer vaccine and found that it contains fragments of DNA. This DNA could potentially cause rare but serious side effects, such as cardiac arrest and future cancer risks. The regulatory process that allowed this contamination is concerning. The DNA could integrate into long-lived somatic cells and potentially cause autoimmune attacks or disrupt tumor suppressors. To produce the vaccine, they cloned the PCR product into a plasmid vector, which led to the contamination. We can easily measure the amount of this substance in the vaccine and should conduct further studies to understand its implications. The FDA should require Pfizer to remove the DNA from the vaccine.

The speaker raises concerns about the contamination of current vaccines with DNA and the unknown consequences of this contamination. They argue that efforts should be made to eliminate DNA contamination, even if it increases production costs. The speaker mentions a researcher from MIT who accidentally discovered that mRNA vaccines were contaminated with DNA. They criticize Pfizer for testing vaccines from one process and then vaccinating billions of people with vaccines from another process, which were contaminated with DNA. The presence of DNA in the vaccines raises risks, including potential cancer development. The speaker believes it is misleading to claim that the vaccines have undergone clinical trials when they have not been properly studied. They call for more rigorous research before commercializing vaccines.

Technology was proven unsafe long before 2021. The COVID-19 vaccines contain lipid nanoparticles that carry synthetic DNA into various organs, risking genomic instability, cancers, autoimmune diseases, and hereditary disorders. Contamination levels are far above permissible limits, and we're seeing evidence in patients. Cancer-free patients are relapsing with aggressive cancers post-vaccination, including unusual and rapid tumor growth. There's a rise in blood cancers too. The vaccines also contained endotoxin, which causes shock and can lead to death. The lab-leak possibility was dismissed without investigation, leading to devastating lockdowns. The "safe and effective" mantra was a lie; these injections have caused unprecedented harm. Ethical principles were ignored, and informed consent was violated. These mRNA gene therapies shouldn't have been used on anyone. We must halt distribution, monitor cancer trends, develop testing, and research vaccine-related conditions.

The recent conference in Perth highlighted serious concerns about messenger RNA vaccines, particularly those from Pfizer, which are reportedly contaminated with SV 40, a substance previously used in tumor research on mice. It's shocking that these vaccines are being administered to humans for a disease that hasn't caused any deaths in two years. Additionally, a deal was announced in Australia for the purchase of $2 billion worth of Moderna vaccines over the next decade, targeting various diseases and intended for children. This raises ethical questions about the motivations behind such decisions, as it seems irresponsible to prioritize profit over the safety of children. The actions of companies like Moderna and Pfizer are seen as deeply troubling, and there is a call for accountability.

Recent findings suggest that DNA contamination in COVID jabs may act as a self-replicating infectious agent. Initially believed to be RNA, evidence shows billions of DNA copies coding for the spike protein in the vials. If this DNA integrates into bacteria or human cells, it could replicate and spread, potentially causing mutations linked to cancer. A case study revealed a patient, who had received four jabs, developed cancer with high levels of plasmid DNA in their tumor. This raises concerns about gut health and the inflammatory nature of the spike protein. It’s crucial to be proactive about detoxifying the gut and maintaining health. Resources and protocols for addressing these issues are available on my website.

Australian lawmakers and officials are admitting they were misled into enforcing coercive vaccine mandates, citing rising deaths and evidence of harm. They are calling for an urgent inquiry and the suspension of mRNA vaccines globally. A New South Wales health minister admitted a link between COVID-19 vaccines and a surge in hospitalizations and heart problems. A lawmaker highlighted synthetic DNA contamination in Pfizer and Moderna vaccines, up to 145 times higher than safety limits, potentially causing cancer and other health risks. Each vaccine shot tested contained trillions of synthetic DNA fragments, including SV40, known to cause cancer. It is claimed that using biological weapons to harm people violates the Geneva Convention. An Australian judge, Helen Rife QC, who dismissed a lawsuit against Pfizer, allegedly failed to disclose her ties to the company. Senator Malcolm Roberts is pursuing those responsible for what he calls the "greatest crime" of the 21st century.

Research has shown that COVID vaccines are contaminated with DNA, including a cancer virus promoter sequence. The DNA can enter the human genome, potentially activating carcinogenic genes and increasing cancer risk. Vaccines suppress immunity, further raising cancer risk. The presence of DNA in vaccines can lead to long-lasting spike production, causing health issues. Vaccines inducing IgG4 antibodies are considered defective. DNA impurities in vaccines can intensify side effects. DNA should not be introduced into the body's cells.

Australia has administered over 60 million vaccine doses to over 20 million people. Despite this, governmental health authorities have chosen not to monitor new or emerging cancer trends, and have failed to make post-vaccination cancer trend data publicly available, which is a critical oversight. Given the massive contamination levels of rogue residual DNA in the Australian vials, we must expect an ongoing rise in cancers and other genetic disorders in Australia. This is a potential long-term health crisis. This matter must be taken seriously. We must advocate for immediate public health responses and monitoring of these trends. Without action, Australians are vulnerable to preventable diseases that may devastate families and strain our healthcare system. These gene-based vaccines should never have been considered. The technology had never been proven to be effective in preventing coronavirus infections and was unsafe long before 2021.

Australia has administered over 60 million vaccine doses to more than 20 million people, yet health authorities have not monitored cancer trends post-vaccination. The lack of publicly available data on these trends raises concerns about public health oversight. Given the contamination levels of residual DNA in the vaccines, there is a potential for an increase in cancers and genetic disorders, posing a long-term health crisis. Immediate public health responses are necessary to monitor these trends and protect Australians from preventable diseases that could overwhelm the healthcare system. The use of gene-based vaccines raises questions, as their effectiveness in preventing coronavirus infections had not been proven, and safety concerns existed prior to their use in 2021.

Decades of research indicate risks associated with foreign synthetic DNA integrating into human cells, potentially leading to cancers and immune disorders. Contamination of synthetic DNA in Pfizer and Moderna COVID-19 vaccines raises concerns about genomic instability. These vaccines function more like gene therapy, as lipid nanoparticles deliver synthetic DNA into the body, risking integration into our genetic material. Since February 2022, there has been a troubling trend of cancer relapses in patients who had been stable for years, particularly aggressive forms of cancer following booster doses. Colorectal cancer is notably increasing in prevalence, along with blood cancers like leukemias and lymphomas. Research indicates that boosters suppress T-cell responses, allowing uncontrolled growth of cancer and other foreign invaders. Concerns about the timing of these cancers following vaccination are widespread among colleagues and patients.

The speaker believes vaccines are causing cancer, with the risk increasing exponentially with each booster, because boosters suppress T cell response, which controls cancer. Experts claim messenger RNA is safe because we are exposed to it daily and it's easily disposed of, but the speaker argues that mRNA vaccines are stabilized to prevent disposal, which is the core problem. The speaker claims that mRNA can integrate and hack your genetic code, promoting oncogenes and down-regulating suppressor genes. They state that the UK and Australia have invested heavily in mRNA technology without proper oversight. The speaker advocates for ending this culture and improving population health.

The Pfizer vaccine contains DNA contamination in addition to mRNA. The DNA comes from the DNA vector used as a template for making the mRNA. Sequencing analysis of the vaccine revealed the presence of DNA, which could potentially cause serious side effects and integrate into the genomic DNA of cells. This poses risks such as autoimmune attacks and potential future cancer. The DNA contamination likely occurred during the production process. It is important to investigate if this DNA has integrated into the genomes of vaccinated individuals. The FDA should require Pfizer to remove the DNA from future versions of the vaccine. The regulatory limit for DNA in vaccines is outdated and not suitable for this type of vaccine. It is necessary to address this oversight and ensure the safety of the vaccine.