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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.

Brooke Jackson, a former clinical trial worker, witnessed numerous instances of malfeasance and misfeasance during her time supervising the clinical trials for Pfizer's COVID-19 vaccine. She observed needles sticking out of bags, private information displayed publicly, patients not being properly monitored, incorrect blood collection methods, and lack of informed consent. The trials were supposed to be randomized and placebo-blinded, but they were neither. The vaccine was not stored at the correct temperature, and baseline data was not collected. Additionally, the data was doctored, certifications were falsified, and fraudulent invoices were submitted to the FDA and the defense department. Jackson reported these issues to the FDA in September 2020.

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 Dutch paper reveals a 36% higher risk of serious adverse events in the Pfizer vaccine group compared to the placebo. Despite this, the public was misled about the safety and effectiveness of the vaccines. Adverse reactions like stroke and heart attack were downplayed, making it difficult to link them to the vaccines. The truth is slowly coming to light, exposing the deception by big pharma, governments, and the media. Those responsible may face consequences in the future.

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.

A girl named Maddie had multiple hospitalizations and ER visits, experiencing numerous adverse events. The EUA amendment reduced her adverse reactions to five, which were diagnosed as functional abdominal pain. The speaker questions if a stomachache would put a child in a wheelchair or require a feeding tube. The CEO or representative from Pfizer was invited but did not attend, and the speaker wonders if Pfizer is aware of their situation. They mention that neither Pfizer, the FDA, nor the CDC has ever contacted or reached out to them.

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)

We found that the FDA lied about a maternal rat study that was testing the safety of mandating a vaccine to pregnant women. In every litter, individual pups had horrible bone deformities. This signal was extremely prominent. Moderna submitted the rat study, as they were required to do. The FDA then lied about the study results by claiming there were no problems. It was a huge enterprise in lying.

A Pfizer whistleblower has revealed documents indicating over 158,000 reports of adverse reactions from December 2020 to February 2021, including serious issues like spontaneous abortions. It is claimed that the FDA was aware of these reactions and sought to keep the documents hidden for 75 years, suggesting intentional harm. The whistleblower argues that the vaccine remains on the market despite serious concerns, highlighting a double standard compared to previous vaccine removals for fewer adverse events. There is a call for accountability for those involved in this situation.

At the outset, a process was approved by the FDA for emergency use authorization. However, it was later discovered that the approved process was swapped out for one containing contaminants like DNA and a cancer-causing substance. Pfizer redacted 800 pages of the manufacturing process, hiding the fact that a carcinogen was included. This lack of transparency led to no informed consent and potential harm to individuals. The vaccine rollout included a trial with a 2.4 times higher adverse event rate, including the presence of a carcinogen.

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.

Speaker 0: I find information like this, you know, inserts for the vaccine. Paper's there, and there's nothing printed on it. I find that very interesting, disheartening, disgusting, and lots of other words, but then it gets better. It just keep wait. There's more. It just keeps happening. The CDC redacts every single word of a 148 page study on a myocarditis after COVID vaccination. So I asked research to print the study for me. 148 pages. The entire thing is redacted. What good does a study do if there's nothing there? Then I wanna know, wait, what might have been there that they needed to redact it? That's even scarier. Speaker 1: We're witnessing an active cover up of a colossal consumer product safety debacle that is is basically affecting the entire world. Mhmm. So in The United States, our CDC, National Institutes of Health, and the FDA are actively involved in a cover up. And the same is occurring in The UK with the MHRA, Europe with European medicine agencies, and Australia with the Therapeutic Goods Administration. Something is going on that's very big. Each one of these companies that puts out a product has an obligation to produce ninety days of safety monitoring after their product comes out. It's a regulatory dossier. If somebody has a problem with the new product and they call the company like Pfizer, Pfizer has to report, write down what happened, and they have to collate that in a report and produce it and make it publicly available. When it came to ninety days with Pfizer, the first vaccine that came out, remember Pfizer was approved 12/10/2020. Pfizer didn't produce the report. And then people started asking, well, what's happening with your vaccine? And Pfizer would not disclose what happened. And then it went to court. And the lawyer for the FDA stepped in and said they don't wanna release Pfizer's dossier for fifty five years. Mhmm. Oh. Fifty five years. And the the the plaintiff pushed. And finally, slowly, the Pfizer dossier came out. Pfizer recorded one thousand two hundred and twenty three deaths with their product within ninety days of release. People were calling Pfizer in desperation watching their family members die after taking the vaccine. Pfizer recorded over twelve hundred new adverse events, new problems that doctor Boden has talked to you about that we are grappling with the entire time. But the point is our FDA worked to cover this up. The FDA should be regulating this company. FDA should have been having at least monthly meetings and fully disclosing what was going on with these novel vaccines, which are a genetic transfer technology platform.

A recent study suggests that Pfizer may have excluded known deaths in the vaccine arm of its clinical trial from its data filing with the FDA in 2020. The study also found that trial subjects vaccinated with Pfizer's COVID-19 vaccine experienced a significant increase in cardiovascular deaths compared to placebo controls. This information was not disclosed by Pfizer when the FDA was evaluating the vaccine for emergency use. Additionally, researchers identified instances where Pfizer attributed potential vaccine-associated deaths to other causes, undermining vaccine safety data. The data presented to the FDA prior to the authorization of Pfizer's vaccine did not include all the deaths that occurred during the trial. The speaker raises concerns about the prioritization of profit over lives and warns against trusting Big Pharma.

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.

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.

A Pfizer whistleblower has revealed documents indicating over 158,000 reports of adverse reactions from December 2020 to February 2021, including serious issues like spontaneous abortions. This raises concerns about the intentional release of the vaccine and the knowledge of its potential to cause severe health problems, including heart attacks and infertility. The FDA's efforts to keep these documents hidden for 75 years suggest awareness of these dangers. The continued availability of the vaccine is alarming, especially considering that other vaccines have been removed for far fewer adverse cases. Those involved in this situation must be held accountable.

Pfizer knew a month into the rollout, November 2020, that this vaccine did not work to stop COVID. Everything that followed—the mandates, the lost jobs, the closures, children not allowed back to school if they didn’t take the shot, the armed forces compelled to take it, pilots compelled—was built on a lie of vaccine efficacy. The most common side effect of getting vaccinated is COVID, and Pfizer understood that the vaccine’s efficacy and vaccine failure showed it did not stop COVID. They also knew the injection did not stay in the deltoid. Europeans through the EMA and public health entities described side effects as chills, fever, fatigue, needing to lie down, but Pfizer knew that was a lie. In Pfizer documents, charts show that the materials—the spike protein, the mRNA, the lipid nanoparticles, and polyethylene glycol—biodistribute within forty-eight hours and leave the injection site to biodistribute to major organs throughout the body, crossing the blood-brain barrier. This may have contributed to personality changes in some loved ones who took the injection. They also accumulate in the liver, the adrenals, the spleen, the lymphatic system, and in women, the ovaries. The first injection accumulates in ovaries; the second injection more so. Experts could not find any mechanism whereby this material left the body in either gender. By the first booster, surgeries on vaccinated women reported fully blocked ovaries, among other damage. Pfizer knew that. They also hired 2,400 full-time staff to process reports of serious adverse events, starting to receive them during the 2020-2021 period. In Pfizer documents, over forty-two thousand serious adverse events were tallied from November 2020 to February 2021, with many individuals experiencing multiple events. The top documented side effects included myalgia (muscle pain), followed by joint pain, then COVID itself, and then a catastrophic tally of serious side effects including heart damage (myocarditis, pericarditis), problems with the aorta, thrombotic events (blood clots in various locations), neurological events (tremors, Guillain-Barré, dementia, epilepsy-like seizures), autoimmune disorders, and eye damage including blindness. Reproductive damage was noted: miscarriages and other issues. Twelve hundred deaths in three months were recorded as not statistically random; they were old with prior conditions, yet doctors noted causality concerns and recorded them. Pfizer knew by April 2021 that minors were injured by the vaccine, specifically myocarditis and pericarditis. Minors sustained heart damage, with thirty-five minors affected. The Israeli Ministry of Health warned the CDC and the Biden administration about minor heart damage, but FOIA requests later showed active conversations up to the White House regarding myocarditis in minors. Instead of withdrawing or advising parents, a 17-page document was produced as a script to persuade parents to vaccinate their minors, supplemented by a TikTok influencer campaign encouraging young people to get injected. These communications indicated that kids would sustain deadly heart damage, and still proceeded. Senator Ron Johnson is using the work to unredact those documents and hold hearings about the cover-up. Pfizer knew all of these things.

A senior scientist at Pfizer in Kyiv reveals alarming details about a COVID-19 vaccine trial for children. Children aged 5-11 were unknowingly given the experimental vaccine, resulting in deaths and hospitalizations. Despite concerns raised, the trial continues with approval from authorities. The scientist is appalled by the lack of regard for children's safety and vows to push for the trial to be halted. The situation highlights unethical practices in medical trials.