reSee.it - Related Video Feed

The speaker claims to have witnessed a humanitarian catastrophe with millions of deaths worldwide due to vaccines. In their private practice, they've seen almost 1500 patients, previously healthy, now disabled and suffering years later, believing they are addressing the greatest unmet need in the country: care for the vaccine-injured. The speaker believes the government has been fully captured by corporations and industrial complexes. They allege that agencies like the CDC, FDA, NIH, and EPA, along with big food, are polluting air, water, and medicines. They also claim the government is allowing immigrants in, surveilling and censoring citizens, and stripping away rights, with most of the country unaware. The speaker states their goal is to educate people about this and "rescue the republic."

RFK Junior announced plans to address the Vaccine Injury Compensation Program (VICP), which was created in 1986 to shield vaccine manufacturers from lawsuits. According to the transcript, vaccine manufacturers, specifically Wyeth (now part of Pfizer), sought legal protection, claiming vaccines are "unavoidably unsafe." This phrase is reportedly in the statute and a Supreme Court decision. Senator Edward Kennedy intended for the VICP to fairly compensate vaccine-injured individuals, but the system is allegedly failing. Kennedy claims the HHS is the defendant, claimants face the DOJ, special masters are biased, there is no discovery, and rules of evidence don't apply. Attorneys report retaliation, fee suppression, and denied access to vaccine safety data. Expert witnesses have allegedly faced intimidation and threats. Kennedy pledges to fix the VICP and restore its original mission, working with AG Pam Bondi and HHS staff. Despite this, skepticism is warranted due to the government's track record on vaccine safety. Concerns remain about rushed approvals, questionable data, and ties with Big Pharma, including recent approvals of potentially dangerous vaccines.

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.

We are discussing a major medical mistake and corporate crime with vaccines causing serious harm like heart attacks and strokes. Research shows the risk of harm from the vaccine is higher than being hospitalized with COVID. This suggests the vaccine should never have been given. It's a scandal that many are unaware of, leading to a pandemic of vaccine injuries.

The speaker discusses the injuries and disabilities that have occurred after receiving the Covid-19 vaccines. They claim that the vaccines were a large human experiment and that the spike protein produced by the vaccines remains in the body for an unknown duration. The speaker suggests that the spike protein is difficult for the body to break down because it is not natural and was engineered in a Chinese lab. They accuse Dr. Anthony Fauci and others of covering up the origins of the virus and suppressing early treatment. The speaker states that about 15% of vaccine recipients have experienced medical problems, including myocarditis and blood clots, even years after vaccination.

The speaker claims there is a connection between autism and government-promoted vaccines, which constitutes a tort, implying many people were injured. They ask how these injured parties can be made whole. Another speaker explains that the 1986 National Vaccine Injury Compensation Program Vaccine Act gave vaccine companies immunity from liability, regardless of recklessness, toxicity, or injury severity. This immunity prevents lawsuits against vaccine companies and is presented as a reason for the increase in vaccinations.

You need to know the risk profile for products like the COVID vaccine. Many discuss adverse effects, but we lack sufficient data, which is unacceptable. Our surveillance system doesn't work. In 2010, the CDC had the Vaccine Adverse Event Reporting System, meant to detect injuries. However, a CDC study revealed it captures less than 1% of vaccine injuries. This is inexcusable. Congress, the Institute of Medicine, and the National Academy of Sciences have repeatedly directed the CDC to develop a better vaccine surveillance system. We will require it and address it immediately.

The speaker discusses the issue of liability protection for vaccine manufacturers and the lack of safety testing for vaccines. They explain that in 1986, liability was taken away from manufacturers, leading to an increase in the number of vaccines given to children. They argue that vaccines should be tested for safety like any other pharmaceutical product, but this is not happening due to the lack of liability. The speaker also addresses the claim that vaccines do not cause injury, particularly autism, and highlights the lack of studies supporting this claim. They conclude by discussing the use of aborted fetal tissue in vaccine development and the objections raised by religious groups.

The speaker claims the medical landscape is dominated by COVID vaccine injuries, disabilities, and deaths, and that they submit multiple entries daily to VAERS, facing scrutiny and potential penalties for falsification. They state they diagnosed an executive in her late thirties with Guillain Barre syndrome from COVID-19 vaccination. The speaker estimates that only 1% of manuscripts on COVID vaccine injuries are being published, suggesting a tremendous bias, and that there are about 4,000 papers on the vaccine debacle, which is about 1% of reality. They claim to have never seen myocarditis, heart failure, or blood clots from eating frosted flakes, but are seeing people devastated by the shots. The speaker advocates for removing COVID-19 vaccines from the market, a critical reevaluation of the vaccine schedule, dropping all vaccine mandates, and rescinding the 1986 Vaccine Injury Compensation Act.

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 vaccine policy will change due to better information. They claim that none of the vaccines given in the first six months of life have been tested, except for the DTP vaccine, which a study linked to issues, but was dismissed due to problems with the CDC's surveillance system. The speaker asserts the CDC lacks a functional surveillance system to capture vaccine injuries, with their own study showing it captures less than 1% of injuries. They plan to fix this by implementing a functional surveillance system, using data management, and providing answers to the public. The speaker promises to follow the science, use gold standard science, publish all datasets, replicate studies, and publish peer reviews, which they claim the CDC has never done, to provide real answers.

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 holds 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.

The speaker discusses the vaccine's link to death and disability, citing over 37,000 deaths globally reported on VAERS. They criticize regulators for not addressing this issue earlier and mention a conversation with Francis Collins about vaccine-related deaths. The speaker also mentions a conversation with Dr. Redfield, who admitted downplaying vaccine injuries to avoid creating hesitancy. Dr. Redfield acknowledged that there are more injuries than reported.

The Countermeasures Injury Compensation Program (CICP) and the Vaccine Injury Compensation Program (VICP) are taxpayer funded. The VICP currently has a $4.3 billion surplus to aid vaccine-injured Americans. However, the VICP is struggling with a backlog of 5,000 non-COVID related claims, which are reviewed by only eight special masters. HR 5142, a bill aiming to modernize the program and update compensation, is projected to cost $10-20 billion. Democrats are hesitant to support the bill due to its vaccine association, while Republicans are unwilling to allocate the necessary funds. This leaves those seeking compensation in a difficult position, as pharmaceutical companies are protected and the government is reluctant to take responsibility.

The speaker states the vaccine recommendation panel has been under attack for 20 years. A 2002 congressional investigation allegedly found 97% of panel members had conflicts of interest with the pharmaceutical industry. One instance cited four out of five members working for a company when they approved its vaccine, and one voting member held a patent on that vaccine, later sold for $186 million. The speaker says the goal is to ensure the panel consists of individuals without conflicts of interest who are not profiting from their votes. The speaker claims that since the panel's inception in 1986, the vaccine schedule has expanded from 11 doses of five vaccines to 69 to 92 doses of 19 vaccines, none of which have been tested for safety. The speaker asserts this is malpractice and aims to ensure all vaccines are tested for safety so physicians and patients understand the risk profile and benefits of each vaccine.

An analysis of clinical trial data showed that for every eight hundred people vaccinated, one suffers a serious adverse event. The goal is to end the silence for the one in eight hundred. It is time to stop politicizing vaccine injuries and start building meaningful recognition, research, competent care, and fair and just compensation.

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.

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.

"And, you know, we're not here to judge anyone that did take a shot." "And in fact, what we need to focus on now is government funding, NIH funding for those who did and are still suffering." "There are a lot of people left in the wake of this program." "However, I think these bold moves give us basically fodder for the cannon to continue to fire and say, look, we will work on better science, better technology, but let's not forget those who were harmed by this." "And we need to focus on better technologies, not gene therapies that go to every cell in the body, not gene therapies for respiratory viruses." "As the secretary said, look, we're for good science. We're not trying to pull everybody's vaccine away from them, but we're not gonna allow them to take unsafe ones."

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.

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.

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.

We have found more adverse effects than officially reported from the COVID vaccine. Serious harms and deaths are at unprecedented levels. We are committed to compensating those affected, but the financial burden should not fall on taxpayers. Our goal is to fight for justice for vaccinated individuals, expose discrimination against the unvaccinated, and reveal the truth about the COVID pandemic and vaccine safety.

Speaker 0: No compensation is available for people with legitimate vaccine injuries, as there is already a system in place through ACC for managing such cases. Speaker 1: However, many vaccine-injured individuals have been denied by ACC and are facing personal financial burdens for their treatment. The requirement of proving the injury is a high bar to meet. Speaker 2: It is not a high bar if a proper examination system is in place. If someone was fine before receiving the vaccine and experienced severe consequences afterward, it is likely caused by the vaccine. We should let an independent commissioner investigate the truth instead of arguing about it.

The speaker claims the current vaccine injury surveillance system, VAERS, captures less than one percent of vaccine injuries, according to a 2010 CDC study. They state that the CDC had a machine counting system to roll out to HMOs but shelved it. The speaker intends to improve surveillance, gather data sets, and create data-sharing agreements with scientists worldwide. They aim to investigate the contribution of vaccines, mold, EMF, food, and other exposures that began in the late 1980s to health issues.