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Twenty percent of Americans did not take the COVID vaccine because it was not safe enough. The mRNA in the Pfizer and Moderna vaccines has been chemically modified to resist breakdown by enzymes. The mRNA and spike protein are found in the heart and brain, and the spike protein circulates in the blood for six to nine months post-vaccination. The speaker claims the lethal part of the virus circulates in the blood of vaccinated individuals, especially after boosters, and that it is a killer protein. The speaker asserts safety trumps efficacy and objects to claims that vaccines, specifically the COVID-19 vaccine, saved millions of lives. They state that consent forms do not guarantee the vaccine will save lives and that there has never been a prospective, randomized, double-blind, placebo-controlled trial showing that COVID-19 vaccines reduce mortality or hospitalization.

The speaker claims Pfizer documents reveal the COVID vaccines didn't work to stop the virus a month after rollout in November 2020. They allege Pfizer knew the third most common side effect was COVID. Within months, Pfizer supposedly needed to hire 2,400 staffers to process adverse event reports. The speaker asserts Pfizer and the FDA knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The speaker states the CDC initially claimed the injection materials stayed at the injection site, but Pfizer knew they biodistributed throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. Pathologist Dr. Robert Chandler allegedly found no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

The speaker believes that halting mRNA vaccine research and development at BARDA is a tragic, non-science-based mistake. They state that mRNA vaccines saved lives, citing estimates that in 2021, unvaccinated individuals were 12 times more likely to be hospitalized and die, and in 2022, six times more likely. The speaker, a member of the FDA vaccine advisory committee, notes initial concerns about potential serious side effects when the vaccine was rolled out to millions, but these did not materialize. While the vaccine can cause rare myocarditis, it is transient and self-resolving, unlike myocarditis caused by the virus itself, which can lead to hospitalization and death. The speaker emphasizes the technology's potential beyond COVID-19, including applications for cancer and gene therapy.

People in America are hesitant to get vaccinated due to the lack of clear information and the speed at which the vaccine was developed. However, one person points out that it used to take years to develop vaccines, but now it can be done in a shorter time frame. Another person argues that nine months is not enough time to trust a vaccine that was created so quickly. The importance of vaccination is emphasized, as it can help stop the spread of the virus. The comparison is made between COVID-19 and the flu, with COVID-19 being seen as more serious due to the higher number of deaths. The conversation ends with one person expressing skepticism about the incentives and fear tactics used to promote vaccination.

People in America are skeptical about the information regarding vaccinations, especially since the vaccines were developed quickly. It traditionally takes years to create a vaccine, and nine months feels insufficient. The conversation shifts to the impact of vaccination on controlling the virus, with one person emphasizing that unvaccinated individuals allow the virus to spread. While some argue that COVID-19 is more serious than the flu, others question the reported death toll from COVID-19, suggesting it may not be accurate. Concerns arise about incentivizing vaccinations, with one person perceiving it as a sign of something suspicious. Ultimately, there’s a belief that the pandemic is driven by fear rather than genuine health concerns.

The organized anti-vaccine movement significantly influenced public perception of the COVID vaccine, leading to an estimated 200,000 unnecessary deaths in the U.S. due to vaccine refusal. This movement targeted individuals and spread misinformation about vaccine safety. In contrast, our low-cost COVID vaccine, developed without a patent, successfully reached 100 million people, particularly in India and Indonesia. However, the primary responsibility for vaccine hesitancy still lies with the organized anti-vaccine efforts.

Speaker 0 asks if Speaker 1 is vaccinated, to which Speaker 1 responds that they are not. Speaker 1 explains that they advised their family and loved ones against getting vaccinated because they believed the vaccine was experimental, not tested on humans, and had concerns about the company behind it. They also mention that most vaccines typically take several years to gather safety data before approval. Speaker 1 expresses their intuition that Operation Warp Speed, the vaccine development initiative, seemed rushed and lacking in safety protocols. However, Speaker 1 did not anticipate the widespread propaganda campaign promoting vaccination, and they were horrified to see everyone around them rushing to get vaccinated without proper testing.

I made it clear that my children were immunized with childhood vaccines. Public health failed to explain that COVID vaccines are different. Childhood vaccines, like for many diseases, provide immunity after one dose by giving children the disease without the deadly consequences. The COVID vaccine wasn't designed to prevent infection. Vaccine hesitancy has doubled since COVID, and we need to address these concerns. The mRNA vaccine should have been prioritized for those at high risk of severe disease, as the science and data indicated. We should have protected the elderly and those with comorbidities first. It went into young people before the elderly and nursing homes. We need to align public health actions with science and data. When we don't, we fracture trust with the American people.

Trump gave Moderna's COO a billion-dollar check to develop a vaccine quickly, bypassing FDA regulations. Human trials began after testing on mice. Many doubted the speed and safety of the process, but the vaccine was developed in 6 months. Concerns were raised by vaccine experts about the rushed development.

Some people love the vaccines, while others hate them. The speaker acknowledges that vaccines have saved lives, but also mentions concerns about their safety. Reports vary on the effectiveness and problems with the vaccines, but the speaker claims to have saved 100 million lives. They argue that those who get very sick and go to the hospital are usually the ones who haven't taken the vaccine. The mainstream media is accused of stifling information about adverse reactions. The speaker believes the vaccines have saved millions of lives but criticizes the media for pausing the Johnson and Johnson vaccine over a small number of cases.

During COVID, I was on the board of my kids' school and initially supported a strict lockdown policy. However, I now realize that keeping kids out of school for longer had a greater negative impact than the risks. We all operated with imperfect information, including myself, the CDC, and the governor. Let's learn from this and hold each other accountable while showing grace and forgiveness. Unfortunately, about 1 in 5 US adults are unwilling to get vaccinated, making them the global runner-up in vaccine hesitancy. This means roughly 56 million Americans are 11 times more likely to die from COVID than the rest of the population. It's embarrassing that some Americans are playing Russian roulette with their lives and the lives of others. Despite this, America's healthcare response to COVID has been a victory, thanks to the vaccines.

Over 100 million Americans were required to get vaccinated due to job mandates. The government claimed vaccines were safe and effective, but data showed vaccinated people could still carry the virus. Despite promises of freedom, there have been 1 million adverse events reported from COVID-19 vaccines, with only 11 compensated cases. Big Pharma has immunity from liability for vaccine injuries.

We are generating real-time data on mRNA vaccines, which have been in development for years due to side effects. Pfizer and Moderna used the pandemic to accelerate their development. The collaboration with BioNTech on flu led to the quick rollout of the mRNA vaccine. Clinical trials skipped phases, causing uncertainty. Concerns arise about vaccine distribution and the need for booster shots. Politics play a role in decision-making.

Speaker 0 and Speaker 1 discuss the COVID-19 vaccine episode, challenging why the vaccine was pursued as a public health solution and exploring deeper incentives behind the program. - A knowledgeable figure at the stand answered a burning question: did they know the vaccine wouldn’t be effective from the start and could be dangerous? The answer given was that it was “a test of a technology.” The exchange suggests the broader aim was testing an entire program of control previewed in Event 2019. - They ask whether inoculation was necessary on billions, noting it could have been tested on a much smaller population. If shots had been basically empty or inert, the data could have been spun to claim success and end the pandemic, preventing injuries from appearing. The absence of that approach remains a mystery. - The speakers point to high pre-vaccine seroprevalence in 2020, including studies from South Dakota showing 50-60% seroprevalence before vaccine release, implying that a saline shot or no shot could have achieved “indomicity” (immunity) without a vaccine. - They discuss why people might fear vaccines and interpret the broader impact: the public is waking up to something terrible having occurred, as it revealed readiness to lie, potential data quality concerns, and risk to pregnant women and healthy children who might get little justification for risk. - The disease’s lethality is framed as greatest among the very old or very sick; for others, it was less deadly, with natural evolution potentially reducing vulnerability over time. - The mRNA platform was touted as a means to outrun mutations, but the timeline to release was still insufficient to stay ahead of natural change. They note accelerated development was the fastest vaccine in history, from detection to inoculation, reducing the timeline by about a year or two, yet not fast enough. - Political and logistical factors delayed release; there is mention that it would not have appeared under Trump and that Eric Topol argued to delay the rollout. Fauci reportedly sent Moderna back to trials due to insufficient racial diversity in participants. - The discussion questions whether the vaccine qualifies as a normal consumer product, given ongoing subsidies, mandates, indemnifications, wartime-like supports, and propaganda. They wonder if there has been an ongoing two-century revolt by industry against public scrutiny, with public interest repeatedly leading to pushback and rebranding. - A central theme is the sophistication of pharma: the “game of pharma” involves owning an IP-based health claim, crafting supportive research, convincing it is safe and effective, achieving standard-of-care status, securing mandates and government funding, and leveraging ongoing propaganda. They describe pharma as a long-running arms race with deep institutional knowledge, implying that it is far more capable of shaping reality than the public realizes.

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.

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 Pfizer COVID vaccine was not tested for its ability to stop the transmission of the virus before it entered the market. The speaker acknowledges that they had to work quickly to understand the situation and move at the speed of science.

The speaker discusses the decision-making process for the COVID vaccine, highlighting the role of Operation Warp Speed and the lack of FDA involvement. They praise the collaboration between NIH and FDA, emphasizing the dedication of the team. The speaker commends the public-private partnership and the effectiveness of Operation Warp Speed. They express a wish for earlier financial support from the government for the industry.

Today, we’ll explore Operation Warp Speed and its historical context. In 1909, Dr. Clark claimed vaccinations caused cancer, noting he never saw cancer in unvaccinated individuals. In 1887, Saint Saviors Cancer Hospital echoed this sentiment. The push for vaccinations dates back to 1885, where financial motives behind vaccines were highlighted. Misinformation about smallpox vaccines emerged in 1880, and in 1799, Dr. Jenner’s smallpox vaccine led to deaths, sparking outrage among medical professionals. A tragic case involved a father whose vaccinated daughter died the next day, symbolized by the Raggedy Ann doll. This history raises questions about the narrative that vaccines can cure cancer.

People in America are skeptical about the information surrounding vaccinations, especially given the rapid development of COVID-19 vaccines. It traditionally takes years to create vaccines, and many feel that nine months isn't sufficient for safety. The conversation highlights the concern that unvaccinated individuals could allow the virus to spread further. While some compare COVID-19 to the flu, the death toll from COVID-19 significantly surpasses that of the flu in recent years. There are suspicions about the motives behind incentivizing vaccinations, suggesting that fear tactics are being used to encourage compliance. Ultimately, the pandemic is perceived by some as driven by fear rather than genuine health concerns.

We discussed pandemic readiness and the speed of mRNA technology. I proposed a simulation to create a vaccine within 60 days, which was initially met with skepticism. However, due to our work on personalized cancer vaccines, we were prepared. When news of a new coronavirus emerged, we quickly got the sequence and began working on a vaccine. The conversation shifted to the need for disruptive entities to accelerate vaccine development, moving away from traditional methods like egg-based production. The urgency for innovative solutions to address outbreaks was emphasized.

Big companies said it wasn't possible, but Trump gave Moderna's COO $1 billion to develop a vaccine quickly. They started human trials after testing on mice. Many were skeptical, but the vaccine was ready in 6 months. Some experts raised concerns about the rushed development process.

We developed vaccines, like the Ameila vaccine, in just nine months. It's fast, considering the uncertainties surrounding vaccines. Initially, we made a mistake by claiming they protect against transmission, but they actually provide limited protection. As a result, repeated vaccinations are necessary due to their relatively short lifespan.

The speaker discusses the development, adoption, and scaling of vaccines for different variants and subvariants. They highlight the speed and extraordinary process of vaccine development. They mention the availability of manufacturing capacity, with a reference to making 100,000 doses in 2019. The speaker recalls a conversation about the need to produce $1 billion worth of vaccines in the following year due to the predicted pandemic. The discussion briefly touches on the topic of new variants and subvariants before the transcript ends.

On COVID, there's a perception that credit isn't given where it's due. While the vaccines were developed quickly, they don't prevent infection or transmission and may have serious side effects. In hindsight, would anything be done differently? Studies on the vaccines are ongoing, and results will emerge over time. It's important to note that Pfizer marketed its vaccine as safe for pregnant women, but reports indicated that over half of the 458 pregnant women who received the vaccine experienced adverse events. The ongoing studies will help clarify these concerns.