reSee.it - Related Video Feed

President Biden, meet Maddie, a 13-year-old aspiring nurse who selflessly participated in the Pfizer clinical trial for the COVID vaccine. Maddie's motivation was to assist her country, but she and others like her have been overlooked by the FDA and the media. The Vaccine Safety Research Foundation questions who will support Maddie after she took a stand to aid America.

Maddie, a 12-year-old who participated in Pfizer's COVID vaccine study, experienced severe health issues after receiving the vaccine. Following her second dose in January 2021, she suffered from debilitating symptoms, including paralysis, seizures, and heart problems. Despite her family's concerns, medical professionals attributed her condition to anxiety rather than the vaccine. While Maddie fought for her life, the FDA approved the vaccine for children, with no mention of her case. The DeGary family felt ignored by Pfizer and health authorities, who failed to acknowledge vaccine-related injuries. Maddie was later diagnosed with a neurological disorder linked to autoimmune reactions. Although there is hope for her recovery, the family's trust in the medical system has been shattered. Federal health officials declined to comment on the safety claims made by Pfizer regarding the vaccine's effects on children.

Speaker 0 states that one of their three children experienced health issues, including heart inflammation, after receiving the vaccine and subsequently lost their job for refusing further vaccination. This adverse reaction is officially registered. The speaker recounts a doctor advising their son against further vaccination outside a hospital setting, but later denying having said so. Speaker 1 says there is a good system for reporting side effects in New Zealand and finds no clear evidence of suppression of medical side effects of the Pfizer vaccine. Speaker 0 questions why the vaccine is still in use given the side effects. Speaker 1 responds that society decided to tolerate a certain number of adverse effects for the greater good, characterizing the speaker's family member's reaction as "taking one for the team."

Speaker 0 described a guest whose 18-year-old daughter was injected with Pfizer and developed cancer. He stated that he has sat across numerous people who lost their children to these injections, with some deaths immediate and others gruesome, and that these people must testify to lawmakers and others recounting their stories repeatedly. He framed this as a massive crime that needs to stop. He asserted that the FDA was fully aware that these injections would cause cancer, citing published guidance documents. He claimed that the FDA regulates the industry and, in 2015 and 2013 (and even more recently), wrote extensive guidance documents explaining to manufacturers developing mRNA products that they must study risks, including cancer, death, fertility issues, blindness, strokes, and cardiovascular issues. He said these risks were documented as regulatory knowledge and that manufacturers were told they had to study these risks and exclude them. He also claimed that studying these risks in healthy volunteers was not allowed because it was considered unethical. He contrasted this with 2020, stating that “all of a sudden, all of this is solved,” calling it a joke, and that this period raised his suspicions, prompting him to investigate independently. He concluded by describing the situation as a premeditated crime in which regulators knew, and that the military conducted a “fake exercise” to capture all these pharmaceutical companies and compel them to create these weapons.

Maddie, a 13-year-old aspiring nurse, volunteered for the Pfizer clinical trial to aid in the fight against COVID-19. However, she and others like her are being overlooked by the FDA and the media. Despite President Biden's assurance of the vaccine's safety, Maddie's selfless act begs the question: who will support her now? This message is sponsored by the Vaccine Safety Research Foundation.

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.

Speaker claims Pfizer knew a month into November 2020 rollout that the vaccine did not stop COVID, and that mandates, job losses, school closures, and two-tier society followed a lie. They allege the injection did not stay in the deltoid; the materials biodistribute within forty eight hours, cross the blood-brain barrier, and accumulate in organs including the liver, adrenals, spleen, lymphatic system, and ovaries, with the second dose increasing ovarian accumulation. Pfizer allegedly hired 2,400 staff to process adverse events, totaling over forty two thousand between 2020 and 2021; top side effects were myalgia and joint pain, followed by COVID. Catastrophic events included heart damage, myocarditis, pericarditis, thrombotic events, neurological and autoimmune disorders, and eye damage, plus twelve hundred deaths in three months. By April 2021 minors showed myocarditis; FDA/CDC/Israeli MOH were aware; FOIA revealed a 17-page script urging parents to vaccinate minors; Ron Johnson uses work to push unredaction.

Maddy DeGary, a participant in Pfizer's COVID-19 vaccine trial for 12 to 15-year-olds, suffered serious injuries post-vaccination. Pfizer initially downplayed her condition as abdominal pain, misleading the FDA. Despite being wealthy, only after an email to FDA officials did Pfizer admit to DeGary's injuries. FDA's response was lackluster, showing no concern for Pfizer's misconduct. The failure to report all adverse events corrupts the trial process, with no repercussions for Pfizer's actions.

Florida's surgeon general raised concerns about the safety of COVID vaccines, while the federal government continues to promote them. This video tells the story of Maddie, a child who participated in Pfizer's vaccine study. After receiving the second dose, Maddie experienced severe symptoms including chest pain, abdominal pain, and loss of feeling in her legs. Despite seeking medical help, her symptoms were dismissed as anxiety. Maddie's case was not properly reported, and the FDA granted emergency use of the vaccine for children based on this study. Other children also experienced serious adverse effects, including heart problems and death. Maddie was eventually diagnosed with chronic inflammatory demyelinating polyneuropathy. The government and those involved in the study declined to comment. Maddie's parents are hopeful for her recovery but have lost trust in the medical system.

The documentary explores potential adverse events following COVID-19 vaccination, focusing on personal experiences of trial participants. Maddie, a 12-year-old Pfizer trial participant, developed severe health issues, including paralysis, after her second dose. Augusto Rue, another participant, reported heart inflammation. Olivia, in a separate trial, experienced nerve pain and suspected lymphoma. Breanne, in the AstraZeneca trial, suffered debilitating pain and neurological issues. These participants claim their adverse events were not accurately reported or acknowledged. Some were diagnosed with functional neurological disorder or post-vaccine neuropathy. Experts re-analyzing trial data found more serious adverse events in the vaccine group than reported. Concerns are raised about the FDA's transparency, fast-tracked approvals, and potential conflicts of interest. REACT19, a support group for the vaccine-injured, was founded to address the lack of support from health agencies. Some studies suggest potential risks like myocarditis, especially in young males. Lawsuits have been filed against Pfizer, alleging misleading claims about vaccine safety and effectiveness. The film highlights the need for further research and support for those experiencing post-vaccination health issues.

Maddie, a 13-year-old aspiring nurse, volunteered for the Pfizer clinical trial to support the COVID vaccine. However, she and others like her are being overlooked by the FDA and the media. The Vaccine Safety Research Foundation questions who will support Maddie after she stepped up to help America.

According to the speaker, Pfizer documents reveal that one month after the vaccine rollout in November 2020, Pfizer knew the vaccines didn't stop COVID and identified vaccine failure. Within months, the company allegedly needed to hire 2,400 staffers to process adverse event reports. The speaker claims Pfizer knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this information wasn't shared with parents until August 2021. The speaker alleges that the CDC initially stated the injection materials stayed in the injection site, but Pfizer knew these materials biodistribute throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. The speaker asserts that there is no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

Researchers are seeking volunteers for a US human trial of a new vaccine. A family shares their experience after their child participated in the trial and experienced severe adverse reactions. The child developed symptoms such as abdominal pain, nausea, fatigue, and neurological issues. Despite multiple hospital visits, doctors dismissed the symptoms as psychological and failed to conduct necessary tests. The child's condition deteriorated, and they are now wheelchair-bound, experiencing pain and other debilitating symptoms. The family feels abandoned by Pfizer and the medical community. A subsequent diagnosis revealed severe nerve damage related to the vaccine. The family hopes to raise awareness and prevent others from experiencing similar hardships. (150 words)

Kelly Sue, a survivor of the vaccine, used to lead an active life but experienced cramping in her calf after her first shot. Concerned, she visited a vascular surgeon who performed an ultrasound on her legs. Weeks later, she had back-to-back strokes and continued to have more throughout the following months. Kelly Sue spent 31 days in the hospital, experiencing various complications such as blindness and difficulty speaking. Her neurologist initially attributed her condition to the vaccine, but discussions about it ceased when doctors started getting fired. Kelly Sue is frustrated that no one is investigating the cause of these adverse reactions. Recently, she experienced a sudden spike in blood pressure and is currently fighting for her life.

President Biden, meet Maddie, a 13-year-old aspiring nurse who volunteered for the Pfizer COVID vaccine trial to help others. While there are many like her, their stories are overlooked by the FDA and the media. You assured the public of the vaccine's safety, but now we need to ensure Maddie's well-being. Who will support her? Paid for by the Vaccine Safety Research Foundation.

A child named Maddie DeGary experienced severe side effects after receiving the COVID vaccine during clinical trials. She felt pain at the injection site and developed intense abdominal and chest pain. Concerns have been raised about the vaccine's safety, with claims of thousands of deaths in the United States. The vaccine's effectiveness has also been questioned, as a reanalysis of the trials suggested a higher likelihood of serious adverse events from the vaccine compared to hospitalization from COVID. Despite heavy promotion and potential coercion, vaccination rates for the booster shot remain low, with only 7% of adults and 2% of children receiving it. Many adults express reluctance to get vaccinated or vaccinate their children.

A child named Maddie DeGary experienced severe side effects after receiving the COVID vaccine during clinical trials. She felt pain at the injection site and developed intense abdominal and chest pain. Concerns have been raised about the number of deaths associated with the vaccine, with claims of 17,000 recorded deaths in the United States alone. A reanalysis of Pfizer and Moderna's trials suggested that the vaccines had a higher likelihood of causing serious adverse events compared to being hospitalized with COVID. Despite these concerns, the vaccines were heavily promoted and even mandated in some cases. Vaccination rates for the latest COVID booster remain low, with only 7% of adults and 2% of children receiving the shot.

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.

This is the story of Maddie, a 12-year-old girl who participated in Pfizer's COVID vaccine study for children. After receiving the second dose, Maddie experienced severe symptoms including chest pain, abdominal pain, and loss of feeling in her legs. Despite her deteriorating condition, doctors dismissed her symptoms as anxiety. Maddie was hospitalized multiple times and diagnosed with chronic inflammatory demyelinating polyneuropathy. The family believes that Pfizer, the FDA, and the study leaders tried to cover up Maddie's case. The FDA granted emergency use of Pfizer's vaccine for children based on this study, but there were no official hearings on vaccine side effects. The family's trust in the government and medical professionals has been shattered.

Maddy DeGary, a participant in Pfizer's 12-15 year old COVID-19 vaccine trial, suffered serious injuries post-vaccination. Pfizer misrepresented her condition as "functional abdominal pain" to the FDA. Despite efforts to bring attention to her true injuries, the FDA showed little concern and failed to hold Pfizer accountable for withholding information. This lack of transparency undermines the integrity of the trial process.

Our next witness is miss Polly Tommy. Miss Tommy is the director of children's health defense. My son, Billy, entered the world as a healthy, perfect baby with an Apgar score that reflected his perfection. The day he received the MMR vaccine hours after the vaccination, Billy's perfect world shattered. He became lethargic, sleeping for long stretches. My husband came home that afternoon and went to check on him, Billy was convulsing. His tiny body gripped by seizures. We rushed him to hospital desperate for answers, but the doctors, after hearing he'd had the MMR said, it's perfectly normal, it's perfectly common. Lots of children have seizures. He'll be fine. No more Pfizer sponsored science.

Yesterday, my last patient of the day, a healthy woman, got the vaccine and the booster. Four days after the booster, she's paralyzed, wheelchair bound. "Really? And four days." "Alan, you and I have been doing clinical trials long enough to know that that's a serious adverse event, right?" "Sure." "Nobody reported it. So nobody's looking at it. It's like, oh, no problem. A good site will eventually report that." "I mean, will eventually have to come out of me because that, I mean, we would Might have reached out to her and tried to mitigate to not have her speak too much." But we're seeing it. "I'm seeing it every day. I mean, I have hundreds of people that have been vaccine injured. So"

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.

Maddie, a 13-year-old aspiring nurse, volunteered for the Pfizer clinical trial to support the COVID vaccine. However, she and others like her are being overlooked by the FDA and the media. The Vaccine Safety Research Foundation questions who will support Maddie after she stepped up to help America.

They received texts claiming extraordinary lives, but the speaker asks how many people have suffered long-term health consequences from the vaccine. The other person, Helen, responds that there have been 10 cases of long-term consequences. In March 2023, MedSafe received 11,289 reports, with 1,062 listed as disabled, 118 as life-threatening, and 184 as deaths. The speaker clarifies if it's 100 or 1,000 cases, but Helen confirms it's around 10 for long-term effects.