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The speaker claims that the evidence around vaccines and autism in the U.S. consists of two flawed and fraudulent CDC studies. One study allegedly showed a statistically significant effect of the MMR vaccine, with 67% more boys receiving the vaccine on time being diagnosed with autism compared to those who waited until age three. The speaker says a whistleblower, Dr. William Thompson, came forward with this information in 2013 and 2014. The speaker also alleges that the Verstraten study in 2003 is flawed and fraudulent, accusing them of cherry-picking information from the Vaccine Safety Datalink. The speaker asserts there is a significant gap in the science around vaccines and autism, stating that safety cannot be determined by looking at one vaccine or component in isolation.

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The speaker questions the safety of 5,000 micrograms for children under six. They claim many vaccine trials use an aluminum adjuvant containing placebo or other aluminum-containing vaccines as the control group. The speaker argues that because the control group receives aluminum, the study is invalidated. They further claim that countries with less aggressive vaccine schedules do not have significant trends in autistic diagnoses. They state that the Amish community, which is largely unvaccinated, has extremely low rates of autism diagnoses.

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We're discussing the presence of mercury in vaccinations, specifically thimerosal, which hasn't been tested by health agencies since its initial test in 1929 on 27 dying meningitis patients. That test found no correlation between their deaths and mercury. Despite its long history of use, there's no conclusive evidence proving its safety. The Institute of Medicine suggests rejecting a causal link between mercury and autism or neurological disorders, but cannot guarantee that trace amounts won't harm children. While one speaker believes it doesn't have the capacity to cause damage, they admit it's impossible to make definitive statements about every child and every dose.

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The discussion addresses whether vaccines cause autism and whether relevant agencies will investigate this. Regarding the MMR vaccine, studies have failed to find a causal link to autism, including a large Danish study comparing vaccinated and unvaccinated children over years, which showed no difference in autism rates. For other vaccines like polio, there's less research specifically examining links to autism. While the speaker doesn't know the full literature extent, they haven't seen the same level of evidence for vaccines other than MMR. Biologically, it's considered unlikely that vaccines are the main reason for the documented rise in autism.

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The speaker asks if there has been a study comparing the health outcomes of children following the CDC vaccination schedule and those who are unvaccinated. The other speaker says they are not aware of such a study and suggests it may be considered bad malpractice not to vaccinate a child. They discuss the possibility of a retrospective study using the Vaccine Safety Datalink, but note the need to control for confounders. The speaker presents an exhibit showing higher rates of health conditions in vaccinated children and suggests the need for larger studies to confirm or refute these findings. The other speaker agrees.

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Thimerosal, a mercury-based preservative, has only been tested once in 1929 on 27 people dying of meningitis, who all died. No other tests have been conducted. The speaker questions why health agencies allow mercury to be injected into people's bodies without testing its safety. The IOM favors rejecting a causal relationship between mercury and autism. When asked if the amount of mercury injected into babies could harm them, the speaker cannot make a categorical statement but believes it is unlikely. The speaker criticizes the health agencies for not removing thimerosal from vaccines despite its toxicity. Progress has been slow in addressing this issue, and the speaker believes the agencies have neglected their responsibility. (136 words)

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The speaker claims epidemiological studies are easily manipulated and that proper studies comparing vaccinated and unvaccinated groups are lacking, except for a CDC study in 1999. This CDC study, led by Thomas Verstraten, allegedly compared children who received the hepatitis vaccine within the first thirty days of life to those vaccinated later or not at all. The speaker asserts the study found a 1,135% elevated risk of autism in vaccinated children, which "shocked" researchers. The speaker alleges the CDC then kept the study secret and manipulated it through five iterations to bury the link.

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The CDC has not conducted studies comparing vaccinated and unvaccinated children over time. In my practice, we analyzed data from all patients over 10.5 years, comparing those who followed the CDC vaccine schedule with those who did not. We included over 500 unvaccinated children and around 3,700 who received some vaccines. The findings were surprising; unvaccinated children experienced significantly fewer health issues, including infections and chronic conditions. The data showed a clear trend: the more vaccines a child received, the worse their health outcomes, including conditions like ADHD and allergies. Shortly after publishing this data, my medical license was suspended, with claims that I posed a threat to public health.

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The speaker discusses the misconception that vaccines are always beneficial and highlights the lower under-five mortality rates in other countries with fewer vaccines. They question why certain vaccines, like flu and varicella, are not widely adopted in other countries and raise concerns about the correlation between vaccines and autism. Another speaker emphasizes the need for an open debate on this topic and criticizes the limited number of vaccines and ingredients studied in relation to autism. They express frustration with doctors who dismiss the potential link between vaccines and autism without thoroughly examining the research. The speaker urges for a more collaborative approach to help children and criticizes those who antagonize the medical community.

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The speaker claims that the CDC commissioned six epidemiological studies using fraudulent techniques, instead of comparing health outcomes between fully vaccinated and unvaccinated groups. According to the speaker, a 1999 CDC study led by Thomas Verstraten compared children who received the hepatitis vaccine within their first thirty days of life to those vaccinated later or not at all. This study allegedly found a 1,135% elevated risk of autism among vaccinated children. The speaker states that the CDC kept the study secret and manipulated it to bury the link by removing older children and stratifying the data. The speaker asserts that over 100 external studies indicate a link between vaccines and autism.

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Autism is caused by vaccines, according to the speaker. The CDC's VirTrak study from 1989 showed a 1350% elevated risk for autism among children who received the hepatitis B vaccine in their first 30 days. A series of 13 studies were allegedly done by people paid by the CDC to create the illusion that vaccines don't cause autism. The chief scientist, Paul Thornsen, is a fugitive wanted by Interpol for stealing millions from the CDC that he claimed to use for the study. His study is considered fraudulent but has not been retracted. The speaker claims there are hundreds of studies linking autism and neurological injuries to vaccines, citing a book with 1,400 references and over 400 studies. The speaker believes the CDC is a dishonest organization owned by the pharmaceutical industry and promotes propaganda that vaccines don't cause autism.

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The speakers discuss the presence of Thimerosal, a preservative containing mercury, in vaccines. Speaker 0 questions why vaccines still use multi-dose vials instead of single-dose vials. Speaker 1 defends the safety and effectiveness of vaccines with Thimerosal but acknowledges the importance of considering the testimony and studies on the potential harm caused by mercury. Speaker 0 challenges the lack of definitive studies disproving the link between Thimerosal and autism. Speaker 1 emphasizes the benefits of vaccines and the challenges associated with transitioning to single-dose vials. Speaker 0 questions why the FDA hasn't taken a cautious approach given the growing evidence. The conversation ends with Speaker 0 expressing frustration and urging the removal of Thimerosal from vaccines.

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The discussion revolves around the use of thimerosal in vaccines and the potential link to autism. The speaker questions why single-dose vials are not used instead. The response emphasizes the safety and effectiveness of current vaccines, despite concerns. The conversation also touches on manufacturing challenges in switching to single-dose vials. The speaker expresses frustration with the lack of definitive answers regarding the safety of mercury in vaccines and advocates for caution in light of increasing autism rates. Ultimately, the debate centers on the balance between vaccine supply and potential risks.

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I raised concerns about investing NIH resources to re-examine the link between the measles vaccine and autism, given the extensive existing research and limited resources. It's impossible to prove a negative, and re-plowing already examined ground distracts from addressing unknown causes or solutions to the chronic disease crisis. We risk children dying from preventable diseases if we keep pretending this link is an issue. I agree that we need to address the rise in autism. While I believe the literature shows no connection between the MMR vaccine and autism, distrust in medicine exists post-pandemic. Providing good data is key to addressing concerns, but I'm unsure what constitutes "good data" when it already exists. The focus should be on pressing childhood health problems like diabetes and obesity, which should be the priorities of the NIH director.

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Kendall asks for an explanation of the process by which the MMR vaccine causes autism, referencing the movie Vaxxed. Speaker 2 responds that they are currently researching those questions, as parents and physicians have reported children developing autism immediately after the MMR vaccine. The speaker claims studies that should have been done long ago were not. Instead, the speaker alleges that captured researchers at the CDC, mainly people who work for the pharmaceutical industry, produced bad epidemiological studies. The speaker asserts that these studies deliberately avoided comparing health outcomes in vaccinated versus unvaccinated groups. Speaker 0 states that this is one of the things they are studying now with gold standard science. Speaker 2 confirms they are doing gold standard science, which includes replication. They are allocating about 20% of their budget to replicating studies. Speaker 0 explains replication as an independent group repeating a study with the same parameters and data sets to achieve the same result. Speaker 2 agrees.

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A congressional committee has concluded that thimerosal, a toxic substance found in vaccines, is directly linked to the autism epidemic. The FDA's negligence in allowing this untested ingredient in vaccines is to blame, driven by the pharmaceutical industry's protectionism. Scientific studies on monkeys have shown that vaccinated primates develop neurological disorders and autism-like behavior. Another study reveals that the mercury in vaccines stays in the brain longer than mercury in fish. Vaccination records also suggest a correlation between increased mercury-containing vaccinations and higher autism rates. Surprisingly, only 4 cases of autism were found among 22,000 unvaccinated Amish individuals, whereas statistically there should have been around 130 cases. Three of the four cases were actually vaccinated, and the remaining individual lived near a power plant.

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The speakers discuss the presence of Thimerosal, a mercury-containing preservative, in vaccines. Speaker 0 questions why vaccines still use multi-dose vials instead of single-dose vials. Speaker 1 explains that the feasibility of switching to single-dose vials is being considered, but there are manufacturing issues. Speaker 0 raises concerns about the potential link between Thimerosal and autism, citing studies and testimonies. Speaker 1 acknowledges the Institute of Medicine's conclusion that the evidence does not definitively support or reject this link. Speaker 0 questions why Thimerosal is still used if there is uncertainty and an increasing autism rate. Speaker 1 emphasizes the importance of vaccine supply and the belief that multi-dose vials are safe and effective. Speaker 0 expresses frustration and urges the removal of Thimerosal from vaccines.

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The speaker questions the safety of Thimerosal, a mercury-based preservative in vaccines, asserting it hasn't been adequately tested since 1929 when Lilly tested it on 27 meningitis patients, all of whom died. Despite this, the speaker claims Thimerosal has been used since the 1930s. The speaker challenges the witness to definitively state that the amount of mercury injected into babies is harmless. The witness admits it's impossible to make such a categorical statement with 100% certainty. The speaker then asks if it's possible that even trace amounts of mercury could neurologically damage a child. The witness says they don't think it has that capacity, but concedes they don't have evidence for every child and dose. The speaker expresses frustration at the difficulty in addressing the issue.

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How many people are completely unvaccinated? It's a small percentage, less than 1%. The Amish community is a notable example, as they largely remain unvaccinated and show very low instances of autism, ADD, autoimmune diseases, and epilepsy. Despite decades of study by the U.S. Government, no public reports have been released. This lack of information likely stems from the potential to undermine the narrative that following vaccination guidelines leads to better health. The absence of such reports suggests that the CDC may have been withholding data that could indicate that not following their recommendations could result in better health outcomes.

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The speaker asked why the FDA and HHS removed thimerosal from most children's vaccines but left it in a few. They admitted not being vaccine experts and offered to investigate and provide more information later. The speaker expressed interest in sharing the answer with the public.

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The speaker states that previous CDC studies on autism were epidemiological and designed to avoid finding a link. They claim the Institute of Medicine criticized the CDC's vaccine schedule decision-making, alleging the ASIP panel was captured by industry due to financial entanglements. The speaker says the Institute of Medicine recommended various studies, including animal models, which the CDC allegedly ignored, opting instead for manipulated epidemiological studies. They claim these studies didn't compare fully vaccinated to unvaccinated groups. According to the speaker, a 1999 CDC study led by Thomas Verstraten found an 1135% elevated autism risk in vaccinated children. They allege the CDC concealed and manipulated this study to bury the link by removing older children from the data and using other statistical tricks. The speaker asserts that over 100 external studies indicate a link between vaccines and autism.

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A congressional committee concluded that thimerosal, a toxic substance in vaccines, is directly linked to the autism epidemic. The FDA's negligence in allowing this untested ingredient in vaccines is blamed on protecting the pharmaceutical industry. Scientific studies on monkeys showed that vaccinated primates developed neurological disorders and autism-like behavior. Another study found that the mercury in vaccines stays longer in the brain compared to mercury in fish. Vaccination records also suggest a correlation between increased mercury-containing vaccines and autism cases. Surprisingly, only 4 cases of autism were found among 22,000 unvaccinated Amish people, when statistically there should have been around 130 cases. Three of the vaccinated individuals and one living near a power plant were affected.

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Speaker 1 states that less than one percent of the public is totally unvaccinated. The Amish are given as an example of a largely unvaccinated group. Speaker 1 claims it is very rare to find an autistic child in the Amish community, and that ADD, autoimmune disease, PANDA PANS, and epilepsy are also rare. Speaker 1 asserts the U.S. government has studied the Amish for decades, but has not released a report. Speaker 1 believes the reason for this is that the report would show that not following government guidelines leads to better health outcomes. Speaker 1 concludes that the report would be devastating to the narrative and would show that the CDC has been harming the public for decades by burying data.

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My name is Dr. Brian Hooker, a vaccine safety scientist. The law shields vaccine manufacturers, and the vaccine schedule has grown to 73 doses by 2023. FDA approved vaccines with minimal safety testing, and CDC never studied the overall impact on children's health. Research shows vaccinated children are more likely to have developmental delays, ear infections, and asthma compared to unvaccinated children. Unvaccinated children have lower rates of autoimmune, neurodevelopmental, and other disorders.

Keeping It Real

VACCINES: HONEST ANSWERS with Dr. Joel Warsh
Guests: Dr. Joel Gator Warsh
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The episode presents a wide‑ranging, data‑driven discussion about vaccines with Dr. Joel Warsh, a pediatrician and epidemiology trained clinician who authored a book aimed at balancing vaccine questions with evidence. The conversation centers on how vaccine safety is communicated, the medical community’s approach to risk, and why concerns persist among parents who notice rising autoimmune and allergic conditions, chronic illnesses, and debates over autism. Warsh stresses that vaccines are not anti‑vaccine; rather, the aim is open dialogue, rigorous safety review, and better public understanding of benefits versus harms. He notes that many questions get short shrift in public discourse, and he advocates transparency, nuance, and ongoing research rather than absolutist declarations about safety being “debunked.” The dialogue dives into core concepts of safety testing and trial design, explaining the difference between inert placebo controls and comparisons against other vaccines or existing vaccines. The guests discuss how safety signals are collected, the role of VAERS, and whether long‑term, large‑scale data can convincingly rule out rare adverse events. They debate the interpretation of data around autism, noting the scarcity of comprehensive, prospective studies across all vaccines beyond MMR and thimerosal and arguing that unanswered questions should prompt more research rather than definitive dismissals. A substantial portion is devoted to the ethical and societal questions of mandates, coercion, and herd immunity. The hosts explore how individual risk assessments intersect with the social contract to protect vulnerable populations, acknowledging that definitions of “safe” and “enough” vary widely. They discuss vaccine technologies—old versus new—and adjuvants, including aluminum and trace metals, as well as the development of mRNA vaccines, their testing history, and what “emergency use” really means. Throughout, the conversation emphasizes the importance of listening to skeptical voices, testing assumptions, and pursuing healthier, safer vaccines while avoiding vilification of dissenting views. The episode concludes with calls for more balanced media coverage and collaborative dialogue among scientists, clinicians, policymakers, and parents to restore trust and improve vaccine safety in practice.
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