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There is a connection between autism and vaccines that the government promoted, and this constitutes a tort, meaning many people were injured by the product. However, in 1986, Congress passed the National Vaccine Injury Compensation Program, giving vaccine companies immunity from liability. Therefore, no matter how reckless the company, how toxic the product, or how egregious the injury, they cannot be sued. This is one reason for the explosion of vaccinations.

In the early 1980s, a tetanus and pertussis vaccine called DTP was used, but it caused brain damage and death in African children. Vaccine companies faced lawsuits and losses, so they went to Congress and threatened to stop making vaccines unless they were granted immunity from liability. In 1986, a law was passed granting them immunity, which eliminated the need for testing and ensured no liability for injuries. This made vaccines a profitable product, as they were mandated for millions of children and had high profit margins. The government purchased a large portion of these vaccines, making it a lucrative industry. As a result, the number of vaccines on the schedule increased from 3 to 72 doses by 1989.

The Institute of Medicine reported in 2011 that over 150 vaccine-related injuries have not been studied, and the CDC has repeatedly been ordered to conduct these studies but has refused. The pharmaceutical companies producing vaccines, such as Merck, Sanofi, Glaxo, and Pfizer, have faced over $35 billion in penalties for misconduct. Trust in these companies is misplaced without solid scientific evidence. While vaccines should remain available for those who choose them, there is a need for rigorous scientific scrutiny. The FDA has misled the public in the past, as seen with Vioxx and opioids, raising concerns about their credibility regarding vaccine safety. The focus should be on ensuring public health, not pharmaceutical profits.

In 1986, the National Childhood Vaccine Injury Act removed liability from drug companies for vaccine-related injuries. Recently, the 9th Circuit Court of Appeals ruled that the COVID vaccine is not a true vaccine as it doesn't prevent disease or transmission. This could open up legal challenges against pharmaceutical companies, though the government may protect them. The outcome remains uncertain.

In the video, the speaker discusses the lack of accountability for vaccine manufacturers. They explain that in the 1980s, there were only three routine childhood vaccines, but now there are 17, with 14 being routine. The speaker highlights that the manufacturers convinced Congress to grant them immunity for any harm caused by their vaccines, leading to the National Childhood Vaccines Act in 1986. This immunity extends to future vaccines added to the childhood schedule. The speaker emphasizes that this level of immunity is not seen in other consumer products, which hold manufacturers accountable for any harm caused. They also mention that emergency youth vaccines, like the COVID-19 vaccine, have separate immunity under the PrEP Act. The speaker argues that this lack of liability disincentivizes safety and affects the conduct of clinical trials and post-market actions by pharmaceutical companies.

A Michigan jury awarded a woman $1 million for being fired over vaccine refusal, highlighting a need for accountability in vaccine manufacturing. It's concerning that vaccine makers have blanket immunity from lawsuits, unlike other businesses. This immunity, granted by Congress in 1986, shields pharmaceutical companies from liability, which is unjust. Everyone else faces risks in their professions, yet these companies operate without accountability. Transparency in government and vaccine trials is crucial to restore trust and eliminate corruption. If information is being withheld, it likely indicates wrongdoing.

Vaccines are unique as the government defends companies against consumer claims in the vaccine injury program. Before 1986, only 3 vaccines were given, but now there are 19, totaling 84 injections. The National Childhood Vaccine Injury Act allowed companies to sell harmful products without consequences. This led to changes in clinical trials and regulatory treatment of vaccines. Regulatory agencies see themselves as partners with manufacturers. Translation: Vaccines are defended by the government against consumer claims. The number of vaccines has increased, and the law allows companies to sell harmful products without consequences. This has impacted clinical trials and regulatory treatment of vaccines. Regulatory agencies see themselves as partners with manufacturers.

Four companies, Pfizer, Merck, Blackstone, and Sanofi, are responsible for producing all 72 vaccines. However, these companies have a history of criminal activity, collectively paying $35 billion in fines for falsifying science, defrauding regulators, lying to doctors, and causing the deaths of hundreds of thousands of people. For instance, Merck's product, Vioxx, was sold as a headache pill but caused heart attacks and killed around 120,500 Americans. Despite this, they only paid fines and faced no jail time. It is hard to believe that these companies, known for lying and cheating, are honest when it comes to vaccines. The vaccine industry is immune to lawsuits, making it the perfect place for these companies to avoid consequences.

Various vaccines are being linked to different industries. The companies behind these vaccines are making a staggering $60 billion annually from vaccine sales. However, they are also making a whopping $500 billion from selling remedies for vaccine-related injuries. This includes medications for diabetes, ADHD (such as Adderall and Ritalin), inhalers like Advair and albuterol, and anti-seizure medications. It seems like a profitable business plan: make people sick and then sell them a lifetime of treatments.

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.

In the early 1980s in the United States, there were only three routine vaccines: DTP, MMR, and OPV, totaling seven injections for childhood, plus the adult and pregnancy schedules, which did not exist at the time. Manufacturers of these three products either stopped making them or went out of business due to injuries and the financial liability associated with those injuries. Typically, when a product harms people, a company would respond by making a better, safer version. The speaker notes that, for vaccines, Congress chose a different path. Instead of compelling manufacturers to improve safety or compensate victims, the United States Congress decided to provide immunity from liability. In 1986, Congress passed the National Childhood Vaccine Injury Act, which granted immunity to manufacturers for liability not only for those three early vaccines but for virtually all other vaccines made thereafter, including all childhood vaccines. The speaker emphasizes the contrast between the standard industry response to harm (improve the product) and the legislative approach taken with vaccines (immunity from liability). The implication highlighted is that this immunity allowed vaccine manufacturers to continue selling products despite injuries, shaping the broader vaccine landscape beyond the initial three vaccines.

Vaccines are not subjected to true placebo-controlled trials before licensure. The DDP vaccine was pulled in the US due to lawsuits against drug companies. Wyeth, now Pfizer, requested full immunity from liability for all vaccines from the Reagan administration in 1986, threatening to leave the vaccine business. The company claimed they were losing $20 in downstream liability for every dollar of profit. When asked to make vaccines safe, they responded that "vaccines are unavoidably unsafe." This phrase is in the statute granting them immunity and was cited in the Brusowitz Supreme Court case. The industry obtained immunity by convincing the president and Congress that vaccines are unavoidably unsafe.

Vaccines are not subjected to true placebo-controlled trials before licensing. The DTP vaccine was pulled due to lawsuits against manufacturers like Wyeth (now Pfizer). In 1986, vaccine manufacturers requested immunity from liability from the Reagan administration, threatening to exit the vaccine business. They claimed they were losing $20 in liability for every $1 in profit. When asked to make vaccines safer, they responded that vaccines are "unavoidably unsafe." This phrase is in the statute granting them immunity and was upheld in the Brusowitz Supreme Court case. The industry obtained immunity by arguing to the president and Congress that vaccines are unavoidably unsafe.

Pharmaceutical companies like Merck, Sanofi, Pfizer, and Glaxo have paid billions in penalties for dishonest practices, resulting in harm and deaths. The opioid crisis and Vioxx are examples of collusion between pharma and regulators, leading to thousands of deaths. Regulatory agencies have become puppets for the industry, depriving the public of informed consent.

Vaccine manufacturers are uniquely protected from design defect claims, unlike manufacturers of other products like planes, cars, and drugs. This immunity was granted in 1986 through the National Childhood Vaccine Injury Act due to the harm and liability caused by the original three routine childhood vaccines (MMR, OPV, and DTP). Instead of requiring manufacturers to create safer products, Congress granted them immunity. This immunity applies to all subsequent routine childhood vaccines. The number of CDC-recommended injections has increased from three in 1986 to 29 today. Pharmaceutical companies developing these vaccines know they won't be liable for injuries. Unlike typical drug trials, vaccine trials often lack placebo controls, have short safety review periods (days, weeks, or up to six months), and are underpowered. These trials cannot confirm the safest product.

The pharmaceutical industry is seen as untrustworthy, being compared to a criminal cartel due to the large penalties they have paid for their other products. Vaccines, however, are exempt from liability, meaning companies cannot be sued no matter how negligent or reckless they are. This lack of accountability may lead to a lack of caution in product development.

The speaker asserts that the 1986 National Child Vaccine Injury Act led to an explosion of creativity in vaccine development due to the immunity from legal consequences it provided to vaccine companies. Before 1986, the 1976 swine flu vaccine fiasco, which resulted in numerous lawsuits and the government indemnifying vaccine companies, set a precedent. The 1986 act, passed due to lawsuits related to the diphtheria pertussis tetanus vaccine, shifted lawsuit coverage to taxes. Over time, the qualifications for compensation narrowed, enriching vaccine companies and allowing them to add adjuvants to stimulate the immune system. This indemnification paved the way for mRNA vaccines. Vaccine trials are now considered a joke, with accepted vaccinated-unvaccinated studies using other vaccines as placebos. Saline placebos are avoided because existing studies allegedly reveal the vaccines' ineffectiveness and increased susceptibility to disease.

Various vaccines are being linked to different industries. The companies behind these vaccines are making a staggering $60 billion annually from vaccine sales. However, they are making an even larger profit of $500 billion each year by selling remedies for the injuries caused by these vaccines. This includes medications for diabetes, ADHD (such as Adderall and Ritalin), inhalers for asthma (like Advair and albuterol), and anti-seizure medications. It's clear that these companies have devised a highly profitable business plan.

Vaccines have never undergone true placebo controlled trials, unlike other medical products. The DTP vaccine was pulled due to numerous lawsuits against drug companies, including Pfizer. In 1986, Pfizer asked the Reagan administration for immunity from liability, as they were losing more money in downstream liability than they were making in profits. Reagan suggested making vaccines safer, but Pfizer claimed they were unavoidably unsafe, a phrase now in the statute and upheld by the Supreme Court. The industry convinced the president and congress that vaccines are unavoidably unsafe, despite claims of their safety and effectiveness.

A law called Vika was passed in 1986, making it illegal to sue vaccine companies, regardless of recklessness or negligence. As a result, the number of mandated vaccines has increased from 3 to 79, none of which have been safety tested. The speaker claims that vaccines are exempt from pre-licensing safety testing, a claim that Anthony Fauci publicly denied. When President Trump appointed the speaker to run a vaccine safety commission, the speaker asked Fauci to provide safety studies on vaccines. Fauci claimed he left them in his office and never sent them. Subsequently, the speaker and Aaron Siri sued Fauci. After a year of stonewalling, HHS provided a letter stating that there has never been a pre-licensing safety study of any vaccine on the childhood schedule.

Pfizer, Moderna, BioNTech, Janssen, and AstraZeneca are accused of withholding safety information and causing deaths. The vaccines distribute toxic spike proteins throughout the body, contrary to what was claimed. Clinical trials were flawed, with unblinded studies and data manipulation. Companies misled about safety and efficacy, offering little virus protection.

Various vaccines are being linked to multiple industries. The motive behind this is money. The companies are earning $60 billion annually from vaccine sales, but a staggering $500 billion from selling remedies for vaccine-related injuries. This includes medications for diabetes, ADHD, asthma, seizures, and more. It's a profitable business strategy: make people sick and then provide them with lifelong treatments.

Various vaccines are being linked to multiple industries. The companies behind these vaccines are making $60 billion annually from vaccine sales, but they are also making $500 billion from selling remedies for vaccine-related injuries. These remedies include diabetes medication, Adderall, Ritalin, Advair inhalers, albuterol inhalers, and anti-seizure medications. It seems like a profitable business plan: make people sick and then sell them lifelong treatments.

Pharmaceutical companies are profiting immensely from vaccines and the subsequent treatments for vaccine-related injuries. They make $60 billion annually from vaccine sales and a staggering $500 billion from remedies for vaccine-induced conditions. This includes medications for diabetes, ADHD, asthma, seizures, and more. It's a lucrative business model: create illness and then sell lifelong treatments.

Vaccine manufacturers are uniquely protected from design defect claims, unlike manufacturers of other products like planes, cars, and drugs. This immunity was granted in 1986 through the National Childhood Vaccine Injury Act because manufacturers of the three routine childhood vaccines (MMR, Polio, and DTP) faced excessive liability and potential bankruptcy due to harm caused by their products. Instead of requiring safer products, Congress granted immunity, allowing manufacturers to continue selling vaccines regardless of potential harm. This immunity extended to all future routine childhood vaccines. Consequently, the CDC schedule has expanded from 3 injections in the first year of life in 1986 to 29 today. Pharmaceutical companies developing these vaccines know they won't be liable for injuries. Unlike typical drug trials, vaccine trials often lack placebo controls (except for the COVID-19 vaccine), have short safety review periods (days, weeks, or up to six months), and are underpowered, making it difficult to confirm product safety.