Despite public statements by government officials affirming the safety and efficacy of COVID-19 vaccines in early 2022, documents obtained by Children’s Health Defense (CHD) reveal that, at that time, public health officials were increasingly concerned about vaccine-related adverse events.
The 300 pages of documents released on Aug. 22 contain private correspondence from 2021 and early 2022 between U.S. Food and Drug Administration (FDA) and National Institutes of Health (NIH) officials, and emails from vaccine-injured individuals to NIH scientists.
CHD requested the documents via a Freedom of Information Act (FOIA) request in 2022. In April 2023, CHD sued the NIH to obtain the records after the agency failed to respond. In an October 2023 settlement, the NIH agreed to produce 7,500 pages of documents at a rate of 300 pages per month.
Last month’s tranche of documents showed that in late 2021 and early 2022, FDA and NIH officials privately expressed concerns about the growing rate of adverse events related to the COVID-19vaccines — concerns that reached high-level FDA officials.
A Jan. 24, 2022, email (pages 239-240) to Dr. Janet Woodcock, the FDA’s principal deputy commissioner of food and drugs, and Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research, alerted them to the existence of “scientific data” regarding adverse events.
The email, titled “Impromptu Meetup” and sent by an individual whose name is redacted, stated:
“We are in [Washington] DC the remainder of today and tomorrow. Some of our epidemiologists happen to be in town as well and would like to have the opportunity to review with you the scientific data they have.
“Also checking in to see what progress has been made with our researchers?”
In a reply later that day, Woodcock said, “We are evaluating the data and analyses that have been done on adverse events after vaccination, particularly neurologic AE’s” (adverse events).
However, she added that the FDA was “not having in person meetings” at that time but stated that “something could be set up for a discussion between the scientists but it would need to be scheduled to ensure the right people attend.” She did not clarify who the “right people” would be.
On the same day, Marks also responded to the email, stating that the FDA has “connected with” NIH researcher Dr. Avindra Nath — who was studying vaccine-related adverse events — and was “also working through contacting other physicians as well.”
Marks added that he “sent a note to our pharmacovigilance group to see if they can free up time today or tomorrow” but said that “setting up a virtual meeting at some point in the near future when there is more time to plan participants and the agenda may make sense.”
There is no indication as to whether this meeting ultimately took place.
The emails followed just months after another NIH scientist, Farinaz Safavi, M.D., Ph.D., of the NIH Division of Neuroimmunology and Neurovirology, appeared to acknowledge the potential dangers of COVID-19 boosters.
In a Sept. 30, 2021, email (page 129), Safavi told a vaccine-injured individual, “We do not have any data to suggest for or against booster shot [sic] but the consensus among our team is not to take if patient develop [sic] significant neurological complications post vaccine.”
The individual emailed Safavi earlier that day asking whether it was advisable to receive the then-new COVID-19 booster, despite saying that “nothing has really changed” regarding their symptoms.“I think my ears are still off, but I have gotten used to it.”
The injured person previously contacted Safavi earlier in 2021 complaining about injuries sustained following vaccination — describing in a March 26, 2021, email (page 136), “severe paresthesias in my face and scalp and tongue and chest band tightness,” and “severe muscle spasms in my scalp and jaw and even my gums and teeth hurt.”
Vaccine injury victims felt ‘very betrayed’
But while some people injured by the vaccines received replies and advice from NIH scientists, the latest documents showed that many others received no such replies. Some sent desperate emails to NIH scientists asking for help or an update.
For instance, in a Jan. 14, 2022, email (pages 234-235) to Nath, a vaccine-injured person praised Nath for his previous work helping the vaccine-injured, but then noted that he and other NIH scientists subsequently abandoned them. The email stated, in part:
“Dr. Safavi left a vaccine injured chat last September, something strange was going on. The active engagement from the spring and summer was replaced with distance and vague responses, then nothing. But then some people get telehealth visits, and vague responses … and others are told ‘there is no research’ and that’s it for them.
“I am sure you would understand now why the hundreds+ who were turned down for any assistance are now extremely upset after waiting for so long … many feel very betrayed. They have been waiting and waiting, all while suffering every single day. … The conversation isn’t happening. They are dying.”
Marks and other FDA officials appear to have met with vaccine-injured individuals a few months prior, according to an Aug. 18, 2021, email sent to Nath (page 283). In that email, the vaccine-injured person wrote:
“Our ‘injured’ MDs and I are meeting with peter marks and paul Richards [sic] at the FDA Monday morning. I have discussed this with Janet Woodcock and Paul for the last few weeks.
“Hopeful they will be willing to help us ‘nobodies’ in our quest to get medical help for people, or any sort of acknowledgement so people are able to begin dialogue with their home physicians.”
Some victims said Marks blew off scheduled meetings with them.
Dr. Danice Hertz, a retired gastroenterologist from California injured by the Pfizer-BioNTech COVID-19 shot she received in December 2020, previously told The Defender that she and a group of vaccine-injured individuals secured a Zoom meeting with Marks in early 2021 — which he then skipped.
Previously released documents from CHD’s lawsuit against the NIH contained emails showing that Marks and Woodcock were aware of reports about COVID-19 vaccine injuries in early 2021, including emails from injured people throughout 2021 and 2022 seeking help regarding their injuries.
Other documents indicate that, as early as January 2022, NIH researchers were aware of at least 850 peer-reviewed case reports and/or research articles about COVID-19 vaccine reactions.
In one email (name and agency redacted), NIH researchers were told the federal government was “saddled” with the “mess” of dealing with those injured by the COVID-19 vaccines, due to the liability shield enjoyed by vaccine manufacturers.
Marks, FDA still publicly claim COVID shots are safe and effective
Marks continues to promote the COVID-19 vaccines as safe and effective and downplay the extent and severity of vaccine-related adverse events.
Last month, he advised the public to get newly updated formulations of the COVID-19 shots, stating the new vaccines “meet the agency’s rigorous, scientific standards for safety, effectiveness, and manufacturing quality.” He said vaccination “continues to be the cornerstone of COVID-19 prevention.”
In a subsequent interview with NPR though, Marks hedged on the question of how effective the new vaccines are.
“The vaccine is not intended to be perfect,” Marks said. “It’s not going to absolutely prevent COVID-19. … But if we can prevent people from getting serious cases that end them up in emergency rooms, hospitals or worse — dead — that’s what we’re trying to do with these vaccines.”
During congressional testimony in February, Marks said, “There was a signal for myocarditis or pericarditis only after the primary vaccination series with the Pfizer mRNA vaccine in those 12 to 17 years of age, and that now that signal is not being seen more recently.”
Marks also claimed that numerous false reports are submitted to the Vaccine Adverse Event Reporting System (VAERS), though other experts have disputed this assertion.
However, Marks also acknowledged that the FDA was overwhelmed with adverse event reports after the COVID-19 vaccines became available, stating that “the avalanche of reports was tremendous.”
The next installment of attorney Aaron Siri’s expert testimony before the New Hampshire House Committee on COVID Response Efficacy. In this episode, ICAN’s lead attorney exposes the shortcomings of post-licensure safety, and shatters the claim that the connection between vaccines and autism has been ‘thoroughly studied.’
A new documentary titled “My Biggest Battle” explores the life-altering journey of renowned
extreme triathlete Heiko Sepp after receiving a COVID-19 vaccination. The 35-minute film
highlights Heiko’s incredible athletic accomplishments, the onset of debilitating health
complications, and his relentless search for answers while suffering from post-vaccination
injuries.
“My Biggest Battle” is more than just a documentary—it’s a conversation starter. Our hope is
that Heiko’s battle encourages the public to share this powerful film to raise awareness about
the challenges faced by individuals like Heiko. By sharing his story, you contribute to an
important dialogue supporting those impacted by vaccine-related events.
The documentary paints a vivid picture of Heiko’s life in Norway, where he lives with his wife
and their two young sons. Known for his remarkable achievements in extreme triathlons,
including podium placements in grueling races like the Norseman, Heiko’s passion for the sport
is central to his identity. However, everything changed in September 2021 when Heiko received
his second COVID-19 vaccination. What began as chest pain rapidly escalated into a series of
debilitating symptoms, including heart inflammation, joint pain, and muscle spasms, leaving
Heiko’s once vibrant life shrouded in pain and uncertainty.
The film follows Heiko’s challenging journey through countless hospital visits, medical tests, and
consultations with healthcare professionals. Despite his lifelong peak health and athletic
prowess, Heiko faces a healthcare system that offers few answers and little relief. As Heiko’s
search for a diagnosis leads him to an esteemed immunologist, the documentary delves into the
emerging understanding of vaccine-induced autoimmunity and its implications for people like
Heiko. The film concludes with a message of hope and resilience, raising critical questions
about vaccine safety and healthcare accessibility.
FUNDRAISER FOR HEIKO’S FAMILY:
Due to Heiko’s illness, he has been unable to maintain stable employment, depleting his
savings on costly private treatments. Facing the brink of bankruptcy, Heiko has launched a
personal fundraiser to alleviate the financial strain and continue his necessary treatments.
Despite the risks, Heiko’s decision to share his story is vital, bringing attention to post
vaccination injuries—a topic few are willing to address.
We urge the media and public to support Heiko’s fundraiser and spread the word about his
story.
Heiko’s story of injury after the first dose and yet still being advised to take a second shot with devastating consequences, is unfortunately a common occurrence. Any doctor will tell you that if you have penicillin allergy you must never receive it again, and yet the medical profession seemed happy to follow this quite extraordinary advice re covid vaccines, as if they couldn’t get the mantra ‘Safe & Effective’ out of their minds. His story of the failures of the medical profession in Norway to diagnose and treat him, is also mirrored across the world.
After a pandemic, all cause mortality should go down due to a culling effect of the frail and vulnerable. We saw acute COVID-19 become the proximate cause of death in many seniors who were in the final year of natural life.
Now an analysis from Allen indicates that all-cause mortality is up in heavily vaccinated Australia and that at least two thirds in the variation per region is explained by mass COVID-19 vaccination. There are numerous well-documented fatal vaccine serious adverse events which are piling up months and years after the shots. Cumulative toxicity is another factor as a single person is not vaccinated just with the primary series (first two injections), but continued dosing every six months.
Allen, DE. 2024. The correlation between Australian Excess Deaths by State and Booster Vaccinations. Medical Research Archives, [online] 12(7).https://doi.org/10.18103/mra.v1 2i7.5485
These data call for a direct data merge of the vaccine administration and death data in Australia to explore these very uncomfortable relationships. Because the Australian government pushed the vaccines so hard, officials have been stonewalling the public on this important next analysis.
Japanese citizens were shocked on the morning of August 28 as their largest national broadcaster, NHK, decided to air a special feature on the COVID-19 vaccine relief system. This program highlighted real-life experiences of individuals who have suffered severe side effects, prompting an overwhelming public response with over 2000 messages received.
In a surprising turn of events, NHK’s popular Morning Show, Asaichi, has taken a bold step. Once dismissive of doubts about vaccine safety, the show recently focused on the challenges and realities faced by those affected by mRNA experimental vaccine side effects. This change in stance marks a pivotal U-Turn in the ongoing national conversation about the experimental mRNA’s safety and transparency.
The program’s new focus was echoed in the unexpected surge of viewer engagement. “We have received more than 2000 messages from viewers today. Thank you very much,” the host announced, signaling widespread public interest and concern.
One chilling account came from a viewer who detailed their struggle after the third vaccine dose: “My headaches became severe. Although they have lessened since the beginning, the symptoms have persisted for more than two years. It has been two and a half years of vaccine aftereffects.” Frustration with the bureaucratic hurdles in seeking relief was evident: “It’s difficult to go collect documents because of my leg pain, so I urgently wish the process to be simplified as soon as possible.”
Another viewer recounted a deeply personal tragedy: “Right after vaccination, my mother developed a serious illness and passed away.” Their story was not just about personal loss, but also about the social repercussions of questioning vaccine side effects. “During the period when I was collecting application documents after my mother’s illness and passing, I’ve been met repeatedly with heartless comments just for questioning the connection with the vaccine.”
The show also featured Misu from Ibaraki Prefecture, a former healthcare worker in her 40s, who shared her ongoing battle. Since receiving her third dose, she has struggled with “pain and numbness in the vaccinated arm, fatigue, and other symptoms.” Misu’s plea was simple yet profound: “I hope the government and media report this properly. Voices are being raised to spread awareness about the suffering caused by side effects.”
This feature on NHK’s Asaichi has not only brought attention to individual struggles but has also highlighted a broader societal issue: the difficulty in openly discussing vaccine side effects without backlash. It presents a call to action for society to foster an environment where sharing such experiences does not invite judgment but rather understanding and empathy.
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Japanese citizens were left stunned when NHK, Japan's largest national broadcaster, on 28th Aug aired an hour long comprehensive report on the harms of the COVID-19 mRNA vaccine.
The program received messages from over 2,000 viewers, revealing that the extent of the… pic.twitter.com/9vlH6LrYhm
Two days following the national broadcast, Japan’s Health Minister, Keizō Takemi, made an unexpected statement: “Regarding whether health damage from the COVID-19 vaccine constitutes drug-induced injury, our response at this point is that we would like to refrain from commenting.”
It looks like they are no longer saying that it is 100% safe and effective!
Novavax is offering parents up to $3,000 to enroll their children in the vaccine maker’s Phase 2/3 COVID-19 vaccine trial for infants and children ages 6 months to 11 years. The offer also includes a stuffed animal for each child.
The “Hummingbird” trial is testing two primary shots and a booster shot of Novavax’s adjuvanted recombinant spike protein nanoparticle vaccine in children. The study, which began in 2022, is enrolling 3,600 children.
The study, which began in the U.S., is expected to run through 2025 and will be conducted in the U.S. and other countries.
The children will receive three injections and visit the clinic eight times. Parents will participate in three phone calls and keep an e-diary of the vaccine’s effects on their child. Some children will receive two additional injections, for a total of five shots.
The study website promises, “You will be compensated for your time and travel regardless of your immigration status. Transportation to the study site may also be provided, as available. No health insurance is required to participate.”
Recruitment materials from Be Well Clinical Studies, which is running one of the U.S. trials, state that compensation can be more than $3,000 over two years.
A 2023 video explaining the study also promises incentives for the children, including “a Covid stuffed animal.”
In the video, a pastor from Louisiana who has four children enrolled in the study said incentives like the stuffed animal made the kids even “more excited than the parents” to participate.
The video features Dr. Jibran Atwi who is running a Hummingbird trial in Lafayette, Louisiana. He encouraged people to participate in the study, because COVID-19 severely affected kids, particularly through lockdowns and lost schooling.
Atwi also said that COVID-19 can be “very disruptive” because if a child has to stay home from school, parents may not be able to go work and the child may have to be isolated from their grandparents.
“Prevention,” he said, “is the best medicine.” He added that there had been an “impressive response” from parents who wanted to participate.
Most of that funding came from Genzyme — a Sanofi subsidiary — and from Sanofi, which shares the co-exclusive licensing agreement with Novavax to commercialize its COVID-19 vaccine.
In 2022, Atwi received over $1 million, largely from AstraZeneca and Genzyme.
Last week, the U.S. Food and Drug Administration (FDA) granted emergency use authorization to Pfizer and Moderna’s 2024-2025 mRNA COVID-19 shots, but Novavax’s 2024-2025 formula has not yet been authorized.
The FDA has authorized previous versions of the Novavax vaccine, but only for children ages 12 and up.
High payments place children ‘at risk of coercion’
Other pharmaceutical companies that have paid research subjects large sums of money have come under scrutiny. In the United Kingdom (U.K.), Moderna was criticized for initially offering children’s families 1,505 pounds ($1,984 dollars) to participate in its NextCOVE clinical trial, which is testing Moderna’s mRNA vaccine in children ages 12 and up.
The Children’s Covid Vaccine Advisory Council submitted a complaint to the U.K.’s Prescription Medicines Code of Practice Authority (PMCPA) — an industry trade group that regulates ethical practices — raising concerns about “inappropriate financial inducement” offered to children and their parents to participate in the trial.
The council cited concerns raised by the research ethics committee (REC) that approved the clinical study. Regarding the 1,500-pound payment they wrote:
“This amount seems much higher than what would be considered a reasonable reimbursement and therefore would contravene clinical trial regulations. The Medicines for Human Use (Clinical Trials) Regulations (2004) explicitly prohibit the giving of incentives or financial inducements to children… or their parents.”
The REC said the amount, “placed the children at risk of coercion,” and the organization required that Moderna reduce the offer before recruitment could begin. Moderna reduced the amount to 185 pounds ($244 dollars).
Yet, according to the complaint, at least one pediatrician continued to offer the high enrollment compensation.
The PMCPA sanctioned Moderna, and the case report on the issue is currently pending.
If the PMCPA determines a pharmaceutical company has breached the industry code, it can require the company to pay administrative charges or issue a corrective statement. Or, it may request a compulsory audit of the company.
In the U.S., Be Well is also advertising that it will pay parents $2,400 for enrolling their infants and toddlers, ages 5-23 months, in Moderna’s Rhyme Trial for an mRNA RSV and a human metapneumovirus (hMPV) vaccine.
According to the clinicaltrials.gov website, Be Well withdrew from the Moderna RSV study, but the website is still advertising to recruit participants.
Be Well is run by founder and director Dr. Mark Carlson, a geriatrician, who has taken nearly $3 million in research funding from Big Pharma, mostly from Moderna, since 2021.
Moderna did not respond to The Defender’s inquiry about compensation offered to children’s families to participate in these studies.
The attorney from the Department of Justice who defended the Food & Drug Administration in court admitted on undercover camera that the agency’s actions were an abuse of authority by the government during its public campaign against ivermectin to treat COVID-19.
A trio of doctors recently won a major legal victory in a multi-year lawsuit sparked by the FDA’s viral 2021 public health guidance advising against the use of ivermectin for treating COVID-19. The most notable offending tweet stated, “You are not a horse. You are a not a cow. Seriously, y’all. Stop it.”
Department of Justice trial lawyer, Isaac Belfer, defended the FDA in this suit brought by Drs. Mary Talley Bowden, Robert L. Apter, and Paul E. Marik. On undercover camera, Belfer admits to a Project Veritas journalist that his client’s legal loss was deserved because the agency overstepped its statutory authority when it publicly tweeted medical advice.
Belfer told our journalist, “So, what the agency has done… [is] unquestionably beyond its authority. Making a recommendation of what drugs to take or not to take, that’s the practice of medicine. And FDA can’t practice medicine.”
The FDA’s public relations campaign also failed to inform the public that the award-winning antiparasitic medicine had a decades-long track record of successful medical usage in humans.
During the COVID-19 pandemic, the doctors prescribed ivermectin to tens of thousands of patients and found the drug to be a cheap and effective treatment.
The doctors told Project Veritas that they suspect that the suppression campaign against ivermectin was motivated by the government’s interest in fast-tracking the experimental COVID-19 vaccination. This speedy vaccine roll-out could only be accomplished through the FDA’s emergency use authorization [EUA], and only if no other alternative medications existed to treat COVID-19.
The FDA’s tweets caused a deadly chain reaction. The agency’s pronouncements were swiftly enforced by national medical associations and regulatory agencies, pharmacists refused to fill prescriptions, insurance refused to pay for it, and doctors who prescribed it faced career ruin.
Drs Apter and Bowden told Project Veritas that suppression of ivermectin led to a prolonged pandemic, and potentially millions in excess COVID deaths.
Apter: “It’s not unreasonable to think that there have been a million unnecessary deaths from COVID in the United States because of the public health agency suppression of effective early treatment with repurposed inexpensive medications.”
Bowden: “If more people had access to early treatment in the form of ivermectin, monoclonal antibodies, hydroxychloroquine… we could have nipped the pandemic in the bud.”
As a result of the lawsuit, the FDA was forced to delete its social media posts warning against the use of ivermectin for treating COVID-19. Though the FDA removed its public statements, the agency did not change its policy or directives. Because major state and national medical governing authorities look to the FDA as an authoritative source on the appropriate use of drugs, pharmacies still refuse to prescribe ivermectin, and doctors face professional repercussions for prescribing it.
Dr. Talley Bowden was forced to resign her privileges from Houston Methodist Hospital; Apter was referred to the Washington Medical Commission and Arizona Medical Board for disciplinary proceedings; and Marik was forced to resign from his positions at Eastern Virginia Medical School.
Apter: “Because of my prescription of ivermectin for COVID I am still facing persecution by the medical licensing boards in spite of the fact that they have not been able to show a single adverse event in my care.”
Bowden: “I have a medical board coming after me because I tried to help a patient get ivermectin. We all had professional repercussions because of our use of ivermectin.”
Though the doctors continue to face professional consequences for their advocacy of ivermectin use for COVID-19, Belfer admits that the doctors dealt a significant blow to the government with their court victory. He told Project Veritas that the agency will think twice before issuing any misguided health advice in the future.
“I think going forward they’ll [FDA] probably be a bit more careful. They [the doctors] got an opinion that was good for them. That kind of limited FDA’s authority. It’s not okay to… actually tell people, ‘You should not take this drug.’”
Dr. Bowden says the fight against government overreach was worth it, because now doctors are vindicated in their years-long quest to protect the health of their patients.
Bowden: “One thing this case did is set a precedent. I think it permanently tarnished the reputation of the FDA. I think the public will takes the FDA little less seriously now, and it keeps them from making the same bold, reckless move in the future when it comes to telling patients what they can and cannot do. Like Isaac [Belfer] said, and we have all said, the FDA is not your doctor. The FDA has no business telling patients what they can take. And we proved in the court of law that they cannot do that.”
The Biden-Harris White House looks determined to justify and normalize the practice of the government colluding with private companies, in this instance Big Tech, to censor speech.
After Meta CEO Mark Zuckerberg on Monday sent a letter to the House Judiciary Committee, admitting that his company came under pressure from the current administration to conduct censorship and that he “believes” that was wrong – the White House doubled down on the controversial, and quite possibly, unconstitutional, policy.
In his letter, Zuckerberg chose to focus on Meta censoring content related to COVID-19, and in response, a White House spokesman revealed the government does not share Zuckerberg’s stance that the policy of pressure was wrong.
“Encouragement” is how that’s phrased. “When confronted with a deadly pandemic, this administration encouraged responsible actions to protect public health and safety,” stated the White House spokesman to media requests.
He further justified the actions described by Zuckerberg as needed because the White House believes private companies, including those from the tech industry, “should take into account the effects their actions have on the American people.”
And with the stage set in this way – the spokesman concluded that these companies are then free to make “independent choices about the information they present.”
But Zuckerberg’s letter to the Judiciary Committee Chairman Jim Jordan does a pretty good job of explaining how these “independent choices” get made. Senior figures from the Biden administration, Zuckerberg stated, in 2021 “repeatedly pressured our (Facebook, Instagram) teams for months to censor certain COVID-19 content, including humor and satire.”
The decision on content removal, and introduction of new rules into platform policies to facilitate censorship, Zuckerberg concedes, was “ultimately ours” – but made under pressure.
If Meta tried to defy these “suggestions” – the administration showed “a lot of frustration.”
“I believe the government pressure was wrong, and I regret that we were not more outspoken about it,” the letter, sent in response to the Committee’s subpoena first issued in early 2023, reads.
The Committee has been investigating how the government may have colluded with private companies to suppress speech it disapproves of, and whether those actions constitute First Amendment violations.
Even before the current Biden-Harris administration came to power, Facebook was being steered in a desired direction, one example being the notorious case of the censorship of the Hunter Biden laptop news story, the Zuckerberg letter reveals.
The FBI contacted the social media giant with a “warning” that there could be an anti-Biden family “Russian disinformation” campaign – and Facebook heeded it by “fact-checking and temporarily demoting (links to the article).”
Award-winning South African political cartoonist and talk show host Jeremy “Jerm” Nell interviews world-class academic Denis Rancourt (h-index 41 & i10 index of 91) on his latest paper showing an estimated 31 million dead from the Covid “vaccines” and the government’s Covid policies. We have a summary of the interview and full transcript at https://artofliberty.substack.com/p/dr-denis-rancourt-31-million-dead
AstraZeneca claims it is not obligated to pay medical expenses for a woman injured by its COVID-19 vaccine during a clinical trial because the company is immune from liability under the Public Readiness and Emergency Preparedness Act (PREP Act).
The British-Swedish vaccine maker is asking the court to dismiss a lawsuit filed by Brianne Dressen, who alleges the company reneged on its contract which promised to compensate clinical trial participants for injuries they sustained.
According to the lawsuit, AstraZeneca’s consent form for trial participants stated, “If you become ill or are injured while you are in this research study, you must tell your study doctor straight away. The study doctor will provide medical treatment or refer you for treatment.”
Dressen alleged she suffered injuries and disability as a direct result of her November 2020 vaccination, resulting in prohibitive medical costs — with one medication alone costing $432,000 a year. AstraZeneca offered her only $1,243.30 in compensation, prompting her to file the breach of contract claim.
In its motion to dismiss, AstraZeneca claimed it is fully immune from Dressen’s breach of contract claim under the PREP Act of 2005, which provides a liability shield to COVID-19 vaccine manufacturers.
“This action is barred by the PREP Act, which renders AstraZeneca ‘immune from suit and liability under Federal and State law with respect to all claims for loss caused by, arising out of, relating to, or resulting from the administration to or the use by an individual of a covered countermeasure,” the motion states.
According to AstraZeneca’s motion, the company did not waive its PREP Act immunity, but if it did, “any waiver would be strictly confined to ‘the costs of medical treatment for research injuries, provided that the costs are reasonable, and you did not cause the injury yourself.’”
AstraZeneca said Dressen’s claim that the company’s COVID-19 vaccine caused her neurological injuries falls outside the scope of such “research injuries.”
“This is a product liability case alleging personal injuries from the administration of AstraZeneca’s COVID-19 vaccine,” AstraZeneca said, seemingly distinguishing between “research injuries” and “personal injuries.”
AstraZeneca also said Dressen’s lawsuit should not be considered a breach-of-contract claim, but a product liability claim — which would preclude Dressen’s claim “under the Utah Product Liability Act’s two-year statute of limitations.”
Dressen’s opposition to AstraZeneca’s motion to dismiss disputed the product liability claim, stating, “AstraZeneca asks this Court to do what no court has ever done: grant ‘complete immunity’ for contractual violations so long as the violations relate to the administration of covered countermeasures under the PREP Act.”
The document cites precedent exempting breach-of-contract claims from the PREP Act’s immunity provisions. “Each court that has addressed claims of immunity for state contract claims has rightfully held that the PREP Act does not apply.”
Dressen also argued that AstraZeneca waived its immunity “by clearly and unmistakably promising to pay the cost of research injuries.”
In a reply brief filed last week, AstraZeneca repeated its original claims. “Plaintiff’s claims fall squarely within the scope of AstraZeneca’s PREP Act immunity and should be dismissed.”
A hearing on AstraZeneca’s motion to dismiss is scheduled for Oct. 29.
‘PREP Act wasn’t intended to excuse such fraudulent and illicit behavior’
The U.S. never granted emergency use authorization for the AstraZeneca COVID-19 vaccine, citing safety concerns.
In its motion to dismiss though, AstraZeneca claimed, “With the protections of the PREP Act in place, AstraZeneca and its partners successfully developed a lifesaving vaccine in a matter of months, an unprecedented scientific achievement.”
Ray Flores, a health freedom rights attorney unconnected to the lawsuit, told The Defender that the PREP Act’s liability shield for “covered countermeasures” extends to products being tested during clinical trials — but not in cases where there has been a breach of contract.
“A breach of contract such as this should obviously be excluded since the PREP Act is essentially a product liability protection statute,” Flores said.
He added:
“I’d like to think the PREP Act wasn’t intended to excuse such fraudulent and illicit behavior. But so far, under the guise of a pandemic emergency, the courts have determined that anything goes.
“This is the first PREP challenge that alleges a viable breach of contract. Since AstraZeneca’s guarantee was in writing, it has an excellent chance of winning.”
According to Dressen, two days after Dressen signed the consent form, AstraZeneca amended the form to state that its vaccine may cause “neurological disorders” such as “demyelinating disease,” which could “cause substantial disability” or death “if not treated promptly.”
Within hours of getting her first dose, Dressen experienced tingling in her right arm — a neurological condition known as paresthesia — and blurred vision and vomiting.
In the ensuing weeks, her condition worsened, with the paresthesia spreading to her legs, resulting in disability and multiple diagnoses indicating her symptoms were related to her vaccination.
Dressen, who was 39 when she was vaccinated, was previously a preschool teacher but is now unable to work.
In May, AstraZeneca announced the withdrawal of its COVID-19 vaccine globally — though the company said it based its decision on the “surplus of available updated vaccines,” resulting in reduced demand for its vaccine.
In an ongoing class-action lawsuit in the United Kingdom (U.K.) against AstraZeneca, plaintiffs allege that they were injured — or their family members died — after getting the shot.
According to The Telegraph, the U.K.’s Vaccine Damage Payment Scheme has approved 175 applications claiming harm caused by the COVID-19 vaccines, at a set amount of 120,000 pounds (approximately $156,000) per claim, adding that “Around 97 per cent of claims awarded relate to the AstraZeneca jab.”
Once again, Labor characterised its foes as ‘conspiracy theorists’, ‘cranks,’ ‘kooks’ and ‘far right extremists’ rather than engaging in rational debate
The Australian Government has voted down a bill to establish a Covid Commission of Inquiry, which would have essentially the same powers and independence as a Royal Commission.
The billwas supported by a small coalition of senators from minor parties and the Opposition (conservative), but was rejected by the Labor Party(left-wing) in a vote today.
To date, Australia has had plenty of Covid inquiries, but none with teeth.
The siloing of inquiries to deal only with states and territory and federal governments on an individual basis has allowed for a lot of finger pointing with very limited accountability.
The scope of the federal Covid Inquiry excludes the policies of state and territory governments, which enacted vaccine mandates, lockdowns and inter-state border restrictions, leading politicians and media to call it “toothless.”
In turn, states and territories have focused on how well they implemented policies heavily influenced by the Federal Government and national advisory bodies without actually considering whether the policies were any good.
The patchwork nature of these inquiries allows the Federal Government to blame states and territories for implementing the harshest measures, and the states and territory governments pass the buck to the federal agencies and departments for influencing them to do so.
Another problem with inquiries to date is that federal, state and territory governments have played hide the ball with important documentation and data required to properly assess their performance. As yet, no Australian government has released the health advice that draconian measures were based upon.
A Royal Commission or similar, taking the entire Covid response – at federal, state and territory levels – and with aggressive powers to command access to information that governments don’t want to release, would be required for real accountability.
The only ways to bring this about are for the executive to call a Royal Commission, or for the Senate to call a Commission of Inquiry.
However, despite the recommendation of the Senate Select Committee on COVID-19 in 2022 that a Royal Commission into Australia’s Covid response be established, the Labor Government has resisted calls to do so.
The Committee, led by senior Labor Party member Katy Gallagher (now Minister for Finance, for Women and for the Public Service) criticised the then Liberal Government’s lack of transparency and accountability around pandemic decision making by the National Cabinet.
Emergency law making had “challenged the Australian Parliament’s capacity to provide meaningful scrutiny of proposed laws, particularly in identifying and addressing the impact of emergency powers on the rights of individuals,” the Committee stated in its recommendations.
Leader of the Opposition at the time, Anthony Albanese, sort of promised a Covid Royal Commission. But after being elected to government in May 2022, Prime Minister Albanese has resolutely dodged the issue, throwing his support behind the limited federal inquiry instead.
The bill, prepared by Senator Matt Canavan (Liberal), was co-sponsored by Senators Malcolm Roberts (One Nation), Alex Antic (Liberal), Gerard Rennick (Liberal), Ralph Babet (United Australia Party) and Matt O’Sullivan (Liberal), all of whom have been vocal critics of Australia’s pandemic response.
During speaking time, senators who sponsored the bill argued that a Covid Commission of Inquiry is needed so that Australia can finally move on from Covid with a good plan in place for future pandemics. A proper inquiry would get to the bottom of what went wrong (and what went right) to restore trust in public health, they said.
Senator Roberts also said that in light of the fact that multiple U.S. states are now suing Pfizer for misleading about its Covid vaccine, if an inquiry found that Pfizer was indeed guilty of fraudulent behaviour, this could shift the financial burden of injuries and deaths associated with Pfizer’s product from Australian tax payers to the pharmaceutical giant.
Australian tax payers have coughed up more than $20 million on compensation for Covid vaccine injuries, but they will have to pay a lot more if a Covid vaccine injury class action is successful. The action, which was filed in the Federal Court last year, has enrolled over 1,500 injured Australians (or families of the deceased).
However, only ten senators supported the bill when it went to a vote in Parliament today. The bill was supported by the above mentioned senators (with the exception of Senator Antic, who is on leave), some members of the Coalition, One Nation, and independent Senator David Pocock.
Despite Greens Senator Jordon Steele-John stating that his party supports the establishment of a “frank” and “transparent” inquiry with the powers of a Royal Commission, the Greens abstained from the vote. Labor voted against the bill.
An inquiry into proposed terms of reference for a Covid Royal Commission has already been conducted, which will prove helpful in the event that either a Royal Commission or a Commission of Inquiry into Australia’s Covid response are eventually established.
Nonetheless, such efforts will face stiff opposition from the Albanese Government, if Labor Senator Tim Ayres’ speech in Parliament today is representative of his party’s position.
In speaking time before the vote, Senator Ayres said that the Government did not support the bill because “there’s already a public inquiry,” before launching into an astonishing diatribe of ad hominem attacks on the senators who proposed the bill.
Senator Ayres used the term ‘conspiracy theories’ or ‘conspiracy theorist’ more than twenty times, likened the efforts of senators to bring about a thorough Covid inquiry to movements motivated by “anti-semitism,” and called these same senators “cranks,” and the “nastiest, extreme, kooky elements of politics.”
Senator Rennick called Senator Ayres’ speech “disgusting,” stating, “all we’re recommending today and supporting is that we have a thorough inquiry.”
In a statement after the vote, Senator Canavan said that more disheartening than Australia’s damaging pandemic response was “the response to the response.”
“Those Australians hurt during Covid deserve to have the accountability of proper public hearings, the publication of all the health advice and an open, transparent attempt to recognise mistakes as well as put in processes to prevent such things ever happening again.
“Why can’t the Government accept that if it is given immense power to lock people in their homes and force people out of work, that there should be an equal and corresponding obligation for them to be accountable to the people hurt by their decisions?”
Senator Babet took to X to express his dissatisfaction with the outcome, calling the decision of the Senate “weak.”
“Is it too much for Australians to ask for governments and the bureaucrats advising them to be held to account for the advice and actions they took during the pandemic?”
When discussing the mRNA COVID vaccines, we need to be careful about dividing people into the two broad groups of the vaccinated and the unvaccinated.
The truth is that many vaccinated people didn’t want to be injected and now deeply regret it.
There are 6 categories of the vaccinated, ranging from the innocent victims to the wicked, unrepentant perpetrators.
1. Those vaccinated by force, against their will
These people were forced to get the jab against their will, and included babies and children who were unable to resist. By forced, we mean they were subjected to extreme duress through threats like job loss or being banned from performing their livelihoods. Many knew that the experimental mRNA shots were potentially dangerous, or didn’t work, and were just unnecessary, but were forced against their will to accept them. These people are victims serious human rights violations. – injured or not.
2. The harassed and coerced
These people were not convinced and many were distrustful of the shot, or even fearful of the drug’s side effects. Many understood that the novel gene-manipulative drug was untested and could be potentially dangerous. Many understood the risk,and never would have allowed themselves to be vaccinated. But they did because the harassment at work, home and in public was just too much to bear.
3. The restriction dodgers
Many were convinced the novel vaccine would work or at least wouldn’t do any harm. Many had felt they didn’t need it, but simply wanted to go back to normal living. Unfortunately these people didn’t do the necessary research to make an informed decision. They were duped into thinking they weren’t harmful. We can forgive this category because at least they didn’t run around lecturing, persecuting and excluding those who resisted taking the mRNA shots. Like in category 1 and 2 above, many deeply regret allowing the injection and promise not to ever take these shots again.
4. The dimwitted follower sheep
They were gullible beyond belief, blindly following everything they were told, and refused to listen to informed experts and hard data contradicting the bogus claims made by the vaccine makers and tyrants. Even today many continue to insist the vaccine works, some even willing to roll up their sleeves again whenever instructed. Too many of them are simply too brainwashed, hypnotized are just flat out too dimwitted to learn. For them, denying is better than confessing and admitting to having been a fool. Yet, we can forgive them to some extent, but we need not give them much sympathy if things go wrong for them.
5. The mRNA vaccine tyrants
We all know who these people are. They were in the media, institutes, governments and big corporations. They lied and hid the risks from us. These people will remain evil until they confess to their grave sins and change their malicious ways. Everyday we heard them ridicule, persecute, marginalize and coerce the unvaccinated. Many of these tyrants need to be punished, prosecuted for fraud, or forever fired from their positions. The late Dr. Vladimir Zelenko even called for the death penalty for the worst offenders. These people can be forgiven, but only through lots of repentance, remorse, apologies and making solemn pledges to redeem themselves.
6. The unrepentant mRNA tyrants
Those who don’t repent must know we will never forget and will not ever relent hauling you in to face legal justice. Your numbers are shrinking and your protection is crumbling. But it’s (still) not too late for you to redeem yourselves.
By B. J. Sabri | American Herald Tribune | April 19, 2016
Since the Korean War, but particularly since the Iranian Revolution of 1979 until today, the United States has been steadily escalating its military presence in the Persian Gulf. Taking advantage of many colossal events of the past 36 years, [1] the hyper-empire has institutionalized its massive presence on land and sea, and expanded its objectives to include the unambiguous physical control of the area, as well as the clear understanding that local Arab governments should abide by them. The pretext is always the same: in “defense” of the national interests and security of the United States. From observing how the United States has been interacting with the governments of the region, and by judging from the size of its expeditionary force, we could reach a basic conclusion. The United States is occupying, de facto, the entire Arabian Peninsula. (Yemen, devastated by Saudi and American jets is yet to be conquered. Oman? Britain returned not as colonial ruler but as a soft occupying power.)
Under this articulation, Saudi Arabia, Qatar, Kuwait, and the United Arab Emirates are virtually occupied countries. If we compare this type of occupation to the mandate and protectorate regimes of the past, the results might be identical—the nations affected by it lose sovereignty. When Arab governments comply with the objectives of a foreign power that station military forces on their national milieu, then that power controls them in multiple ways including how they react to policy deliberations and what decisions they intend to take on specific issues. A good method to verify the concept of effective occupation is this: take notice of what the United States says and wants, and then compare it to what the gulf rulers do in response. (I shall discuss this detail at some point in the upcoming parts.)
If the presence of US forces or other means of political pressure are a factor in Saudi Arabia’s interventionist Arab wars, then we need to debate this issue. However, from the history of resistance to colonialism, we learnt: if a powerful state imposes its order on a nation by military means or other forms of coercion, and if this nation does not resist that imposition, then a mental subordination to the powerful state will ensue. This is especially true in the case of Saudi Arabia. One single event, 9/11, has transformed it from a US “ally” into an instant political hostage of the American Empire. … continue
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