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The speaker believes that the representation of COVID-19 vaccines as vaccines is false. They argue that the FDA has no regulatory authority over these countermeasures, and that the manufacturers engaged in fraud and data manipulation. They claim that there is documented data showing significant injury and death, which Pfizer was aware of. The FDA's assertion that the vaccines are safe and effective is seen as play-acting.

"dreadful use of vaccines and the mandates that have caused so much problem." "From the very beginning, these vaccines were not vaccines, particularly the ones that ended up after AstraZeneca with all the clots and they were shut down." "The messenger RNA vaccines of Pfizer and Moderna, of course, unbelievable problems and damage to people." "They were pushed into this by Pfizer and all the people that Pfizer and Moderna wanted to get this into everybody." "These were not vaccines. These were horrible gene therapies that could actually integrate into your genome." "turbo cancers." "They are incompetence, medical negligence, everything, and nobody is accepting responsibility for this." "This is Nuremberg trial stuff." "They were never ever effective." "There was no evidence that they were effective whatsoever. It was basically hope, and they were never ever safe."

According to VAERS, there have been 38,000 deaths from COVID shots. The speaker claims that under normal circumstances, the FDA would have pulled the shots, but instead, they've been put on the childhood vaccine schedule, with babies expected to get three shots by nine months old. The speaker states the shots are still under EUA status for those 12 and under, and are not fully FDA approved, yet are on the vaccine schedule. According to the CDC, nine million American children have received the latest version of these COVID shots. The speaker expresses concern about myocarditis in children. The speaker believes the shots should have been shut down a long time ago.

Today, we are here to inform the public and representatives about the serious errors and safety issues related to mRNA injections. The previous speakers discussed the deadly political mistakes made by the EMA and the European Commission, who deliberately deceived the public and used pseudoscience to push people into potentially deadly experiments. The EMA admitted to providing misleading information to the public, and the lack of evidence for transmission control makes the vaccination campaign a fraudulent and illegal marketing campaign. The argument that this is for the benefit of vulnerable and elderly individuals is false, as the entire population has been forced to participate in this potentially deadly experiment. We demand the removal of all mRNA injections from the market and accountability for those responsible.

The COVID special committee revealed significant misinformation regarding the mRNA injection. Claims that it saved 20 million lives were exposed as false; that figure actually refers to all vaccines in history, not just the mRNA injection. In reality, it is suggested that the mRNA injections may have contributed to the deaths of 17 million people globally. There is no evidence to support the notion that these injections are safe and effective, as they were never properly tested.

I'm Christine Drivdahl Smith, a family physician and volunteer board member of the Montana Medical Freedom Alliance. Gene-based vaccines, including COVID-19 shots and a new RSV shot, are the most destructive medical products ever used. I urge you to support a bill banning them to prevent further harm and death. These vaccines were rolled out under emergency use authorization, which has been extended to 2029, shielding manufacturers from liability. Despite over 38,000 deaths reported to VAERS and thousands of peer-reviewed studies documenting injuries like cardiac arrest and cancer, these vaccines remain in use. Highly vaccinated countries are experiencing increased mortality and decreased life expectancy. The shots don't prevent disease and are contaminated with excessive DNA, increasing cancer risk. Shedding of these vaccines has been confirmed. The American College of OBGN still recommends them for pregnant patients, and the CDC has added them to the pediatric schedule.

Today, we are here to inform the public and representatives about the serious errors and safety issues related to mRNA injections. The previous speakers discussed the deadly political mistakes made by the EMA and the European Commission, who deliberately deceived the public and used pseudoscience to push people into potentially deadly experiments. The EMA admitted that the information provided to the public was not for informed consent. The lack of evidence for transmission control from the start makes the vaccination campaign a fraudulent and illegal marketing campaign. The argument that it is a disservice to vulnerable and elderly individuals is false, as the entire population has been forced to participate in this potentially deadly experiment. We demand the removal of all mRNA injections from the market and accountability for those responsible.

"72 mandated vaccines by the age of 18." They start injecting pregnant women second trimester. "In 1986, congress gave big pharma carte blanche, put in whatever you want. You have absolutely no liability." "And in that year, the vaccine schedule tripled." "Babies are getting seven shots at the same time." "This shot is experimental and on and you it did not get FDA approval. That was a complete fraud." "under an EUA, emergency use authorization." The synthetic mRNA is a program that they put into your body. It instructs your cells to produce the spike protein. The spike protein in itself creates the disease. It also contains fetal cell lines, kidney cells, retinal cells, lung cells. These are immortal meaning that they are cancerous. The COVID contained polyethylene glycol. Seventy percent of people are allergic to this. Luciferase. The shot contains a bioluminescent dye.

Hello, I’m Dr. Mike Geadon. I want to address those affected by vaccine injuries and those involved in politics. I believe the materials labeled as vaccines were intentionally designed to harm recipients. With a background in pharmaceutical research, I assert that the COVID-19 response was based on misinformation, leading to unnecessary deaths due to harmful medical practices. The so-called vaccines were rushed and inherently toxic, targeting the body’s immune system and potentially harming fertility. This was not a mistake; it was a deliberate act by powerful entities seeking control. We must stop trusting those who lied to us and speak out against these actions. Politicians must recognize the gravity of their decisions regarding public health legislation. If we remain silent, we risk losing our freedoms and lives. Speak out, no matter the consequences. Thank you.

I recently heard stories of people losing their children to Pfizer injections, some experiencing immediate or gruesome deaths. The FDA knew about potential risks like cancer from as far back as 2013, but suddenly in 2020, these concerns were ignored. This seems like a premeditated crime, with regulators aware of the dangers. Military involvement in pushing these products is suspicious.

Elected officials are not acting in the people's best interest, serving pharmaceutical companies with the mRNA shot. They all use the same script, talking about safety without considering the risks of the injection. The vaccination campaign will be remembered as the biggest medical scandal and crime against humanity.

The speaker describes a committee conflict investigated by the office of inspector general and Congress, who urged change, but nothing happened. They claim medical malpractice by this group is evident in the approval of vaccines. The speaker states that in 1986 there were 11 vaccines, which increased to 69, then 92. They assert that, except for the COVID vaccine, none had a pre-licensing safety trial involving a true placebo. According to the speaker, these vaccines were introduced without safety studies, resulting in a lack of understanding regarding the risk profiles of these products. The speaker attributes this to corruption and agency capture.

The speaker states that many people have been injured by the COVID vaccine, some fatally or permanently disabled, and that these people are not receiving sufficient care or attention. The speaker says that the 1986 Vaccine Act is a major impediment to change. According to the speaker, Congress recognized that vaccines were "unavoidably unsafe" when it granted vaccine companies immunity, so it created a federal program with a trust fund to compensate those injured. The program is funded by a 75% surcharge on every vaccine. The speaker says the vaccine court is supposed to be generous and fast, but the speaker believes the lawyers defaulted to protecting the trust fund instead of taking care of people. The speaker says the program has paid out over $5 billion to about 12,000 people. The speaker says they are looking at ways to enlarge the program so that COVID vaccine-injured people can be compensated, including enlarging the statute of limitations.

I recently met someone whose 18-year-old daughter developed cancer after receiving the Pfizer vaccine. I've heard from many parents who lost children to these injections, some experiencing immediate and horrific deaths. They repeatedly share their stories with lawmakers, highlighting a significant crime that must end. The FDA was aware of the potential cancer risks associated with these vaccines, as outlined in guidance documents from 2013 and 2015. These documents instructed manufacturers to study risks like cancer, fertility issues, and cardiovascular problems, and deemed it unethical to test on healthy volunteers. Yet, by 2020, these concerns were seemingly overlooked. This raises serious suspicions about the intentions behind the vaccine rollout, suggesting a premeditated crime where regulators and the military may have colluded with pharmaceutical companies.

There have been repeated attempts to mandate coercion without accepting natural immunity, which is claimed to be equally effective at preventing infection and more effective at preventing severe disease and death. There was no real questioning of an emergency use authorized product, and informed consent was not prioritized. When doctors make mistakes, they should acknowledge the mistake and harm, apologize, and institute measures to prevent recurrence. This hasn't happened at a public health scale, and the medical establishment needs to acknowledge the problem. The speaker believes the product in question should never have been approved for a single human. At the very least, there should be acknowledgement of unintended harms, apologies, efforts to help the vaccine-injured, and structures for greater transparency in medicine. Regulators should not receive 86% of their funding from big pharma and then claim to be independent.

The Trump administration's Operation Warp Speed developed a COVID vaccine quickly, but critics argue that the program protected drug companies from liability for vaccine injuries. The government's compensation program for harm caused by vaccines has been criticized for being bureaucratic, with only 8 payouts out of 12,000 claims filed. The issue of liability for vaccine manufacturers has been a topic of debate since Reagan's presidency. Some argue that those harmed by vaccines deserve accountability and that free speech is crucial in discussing the merits of vaccines. There is a call to end crony capitalism and lobbying in government, with a focus on preventing government officials from joining companies they previously dealt with. The government's actions during the COVID-19 pandemic, including vaccine mandates and the approval of mRNA shots for young babies, are seen as problematic. There is a desire for accountability and a promise to clean house in agencies like the CDC, NIH, and FDA to prevent similar situations in the future.

The speaker claims COVID vaccines are not actually vaccines and have caused unbelievable problems and damage. They allege the virus escaped from a lab with six manipulated inserts and the vaccine was 80% homologous to humans, causing major side effects. The speaker states that governments were informed but ignored warnings. They further claim the vaccines' quality control was appalling, the manufacturing process changed, and they were full of contaminants that can integrate into the genome, leading to massive excess deaths and a rise in cancer. The speaker questions why the vaccines haven't been banned, given COVID's diminished threat. They criticize the vaccination of children and call the vaccines "horrible gene therapies" causing "turbo cancers." They advocate for trials for those involved and accuse medical officers and regulatory bodies like MHRA, TGA, and FDA of incompetence and negligence, likening the situation to the Nuremberg trials. They assert the vaccines were never effective or safe, citing Pfizer's initial submissions to the FDA.

I am a toxicology expert who has worked on designing experimental molecules for medicines. Based on my expertise, I firmly believe that the materials used in these vaccines were intentionally designed to cause harm, injury, and reduce fertility. I will be presenting this argument in court soon. Therefore, I strongly advise against taking these injectables or any future mRNA-based materials as they are all dangerous. Additionally, we have all been deceived from the beginning, as there was never a true pandemic or public health emergency. The media and unreliable diagnostic tests have spread lies and propaganda.

The speaker claims a committee experienced typical conflict, but a specific conflict was particularly obvious. The Office of Inspector General and Congress investigated and urged change, but nothing happened. The speaker asserts this group committed medical malpractice by approving vaccines, increasing the number from 11 in 1986 to 69 and then 92. They state that, except for the COVID vaccine, none had pre-licensing safety trials with a true placebo. According to the speaker, these vaccines were introduced without safety studies, meaning the risk profiles are unknown. The speaker attributes this to corruption and agency capture.

The speaker questions how many people injected with mRNA products knew they weren't receiving a traditional vaccine, suggesting many, including medical professionals, are unaware due to the perception of conspiracy. The speaker claims there was a sufficient safety signal in VAERS to halt the rollout in January, citing almost 90,000 VAERS entries and nearly 700 deaths within the first month. They state that historically, products causing over 50 deaths have been pulled from the market. The speaker questions why the CDC, HHS, and FDA aren't investigating this data.

Speaker decries the use of vaccines and mandates, questioning why it was done. They claim, "these vaccines were not vaccines" and that "the messenger RNA vaccines of Pfizer and Moderna" caused "unbelievable problems and damage to people," and were "pushed into this" by Pfizer and Moderna. They state, "These were not vaccines. These were horrible gene therapies that could actually integrate into your genome," linking to a rise in "turbo cancers." They urge others to "stand up to trial, defend themselves, and go to court" and call it "Nuremberg trial stuff," alleging "incompetence" and "negligence," that "they were never ever effective" and that there was "no evidence that they were effective whatsoever" and "they were never ever safe."

We were deceived with false information about the safety and effectiveness of these products. The claim that they would remain at the injection site and lymph nodes was proven false. The modified RNA in these products was said to only last a short time, but we now know it remains active in the body for weeks or even months. We were also manipulated into believing that we all needed to be vaccinated for everyone to be safe, using illegal tactics like coercion and enticement. These lies were used to justify the deployment of these experimental products, which aimed to establish a profitable vaccine platform technology.

A physician who experienced an adverse reaction to the Moderna COVID shot states that the COVID shots should never have been authorized for children and pregnant women. After receiving the Moderna shot, the speaker developed transverse myelitis, autonomic dysfunction, and an unspecified immune disorder, leading to medical retirement. The speaker is now co-chair of React19, representing Americans injured by the COVID shots. The speaker claims that the clinical trials were rushed, safety data was withheld or altered, and reporting systems like VAERS and V-Safe have failed. The speaker questions whether regulatory agencies have a conflict of interest. The speaker alleges that instead of proving safety and efficacy, the COVID-19 shots were assumed to be safe and effective, with short follow-up data, and were given to pregnant/lactating women and children without long-term safety data. The speaker is appreciative that the COVID-19 shots have been removed from the childhood vaccination schedule for healthy children, but much damage has already been done. The speaker advocates for recognition, research, medical care, and compensation for those injured by the COVID-19 shots.

Doctors and politicians have promoted vaccines, but refuse to acknowledge potential harm. Many Americans who received the vaccine may face unknown risks. The truth must be revealed to prevent future harm from the mRNA platform.

None of the vaccines, including the COVID vaccine, have undergone proper testing. No childhood vaccine has completed a placebo-controlled clinical trial with sufficient duration and power to confirm its safety before being administered to millions of children in America. This is not an opinion; it can be verified by anyone visiting the FDA website, where the package inserts and clinical trial documents are available for review.