VAERS – American Conservative Movement https://americanconservativemovement.com American exceptionalism isn't dead. It just needs to be embraced. Sun, 24 Sep 2023 18:02:04 +0000 en-US hourly 1 https://wordpress.org/?v=6.6.2 https://americanconservativemovement.com/wp-content/uploads/2022/06/cropped-America-First-Favicon-32x32.png VAERS – American Conservative Movement https://americanconservativemovement.com 32 32 135597105 How Myocarditis Became the Silent Scandal of Covid “Vaccination” https://americanconservativemovement.com/how-myocarditis-became-the-silent-scandal-of-covid-vaccination/ https://americanconservativemovement.com/how-myocarditis-became-the-silent-scandal-of-covid-vaccination/#respond Sun, 24 Sep 2023 18:02:04 +0000 https://americanconservativemovement.com/?p=197088 (Rational Ground)—It started slowly at first – a trickle of concerning reports that something wasn’t right. In January 2021, just weeks after the rollout of the COVID-19 vaccines, cases of myocarditis began cropping up.

Myocarditis – inflammation of the heart muscle – had never been linked to vaccines before. So when 28 cases were reported to the US vaccine adverse event reporting system (VAERS) [1] that month, it raised eyebrows..

By February, the trickle had become a stream. VAERS received 64 more reports, including two deaths [2]. Then in March, Israel [3] and the military [4] started reporting cases too.

Something strange was going on. But the authorities ignored it.

In March, the FDA authorized the Johnson & Johnson vaccine without a whisper of myocarditis [5]. The CDC soon recommended it for all adults [6]. Colleges and businesses started mandating the shots [7]. It was full speed ahead.

Behind closed doors though, alarm bells were ringing. The CDC met with the military to discuss the myocarditis cases in young troops [8]. Israel was reporting dozens of cases, including in teenagers [9]. The FDA knew from Pfizer that there were nearly 60 cases already in its database [10].

But in public, it was denial and dismissal. The CDC director claimed she wasn’t aware of any military cases [11]. Pfizer hid its database numbers [12]. And the FDA rubber-stamped authorization of the Pfizer vaccine for teenagers in May without a mention of myocarditis [13].

As myocarditis reports flooded into VAERS in the hundreds during the summer [14], young, healthy people continued being pressured to get vaccinated. Mandates rolled out across the country [15]. The authorities told the public the benefits outweighed the risks [16].

But patients started sharing their stories of being hospitalized with heart problems after vaccination [17].Researchers began publishing case reports in medical journals [18]. And still, the CDC publicly downplayed concerns [19].

Behind closed doors, officials strategized about monitoring the alarming reports [20]. They expanded the criteria for identifying myocarditis cases [21]. More hospitals confirmed seeing unusual cases in vaccinated youths [22].

In June, the FDA quietly added warnings about myocarditis to the vaccine fact sheets [23]. The news dripped out slowly that CDC advisers now acknowledged a “likely association” [24].

But the full scope remained obscured. The authorities clung to the narrative that benefits outweighed risks [25]. They used incomplete data and rosy assumptions to claim the vaccines were still worth it for young people [26].

Millions of teenagers continued getting pressured to get vaccinated throughout the summer and fall [27]. It became painfully clear that the drive for widespread vaccination took precedence over transparency and caution.

It wasn’t until October 2021 that the warnings were taken more seriously. Nordic countries limited the Moderna vaccine due to myocarditis concerns [28]. The FDA and CDC were forced to address the risks more openly in meetings [29].

But still, they pushed ahead with expanding the shots to younger ages [30]. Five-year-olds started getting vaccinated in November despite a complete lack of safety data [31]. Booster doses were promoted for teenagers against the advice of their European counterparts [32].

The evidence continued piling up into 2022 that the vaccines were inflaming hearts [33]. Young people, almost all male, were suffering severe outcomes [34]. The FDA fully approved the Moderna and Pfizer vaccines with scarcely a mention of myocarditis[35].

Regulators around the world scaled back recommendations for boosters in young people as more safety signals emerged [36]. But the US charged ahead, even permitting a fourth dose before any trial data was available [37].

Three years and over 1,600 confirmed VAERS reports later [38], the CDC finally admitted publicly that the mRNA vaccines cause myocarditis [39]. But authorities continue maintaining the stance that benefits outweigh risks across all groups [40].

Yet as researchers report finding heart abnormalities months later [41], it’s unclear if the full scope of risks is known. Some experts argue society lost sight of “First, do no harm” in the rush to vaccinate an entire population against COVID-19 [42].

Why were the early warning signs dismissed? How many ended up harmed from ignored or hidden signals [43]? And why does debate about vaccine prudence remain taboo despite mounting evidence condemning overly broad immunization policies [44]?

This story is far from over. As more studies probe long-term effects and deaths possibly caused by vaccine-induced myocarditis [45], questions will continue swirling.

The families forever changed want accountability. Recognition that mass vaccination programs failed to uphold informed consent [46]. And assurances that blindly “following the science” won’t again take precedent over individuals’ health [47].

Myocarditis turned out to be the tip of the iceberg when it came to underestimated vaccine risks [48]. Only time will tell the full scope of lives upended and lost in the race to inoculate the world [49].

Leave you thoughts about this story on the End Medical Tyranny Substack.

Props to Epoch Times for their detailed timeline on all of this!

About the Author

Justin Hart is an executive consultant with over 25 years experience creating data-driven solutions for Fortune 500 companies and Presidential campaigns alike. Mr. Hart is the Chief Data Analyst and founder of RationalGround.com which helps companies, public policy officials, and even parents gauge the impact of COVID-19 across the country. The team at RationalGround.com offers alternative solutions on how to move forward during this challenging pandemic.

]]> https://americanconservativemovement.com/how-myocarditis-became-the-silent-scandal-of-covid-vaccination/feed/ 0 197088 The Global Depopulation Agenda Is More Organized and Well-Funded Than Ever Before in World History https://americanconservativemovement.com/the-global-depopulation-agenda-is-more-organized-and-well-funded-than-ever-before-in-world-history/ https://americanconservativemovement.com/the-global-depopulation-agenda-is-more-organized-and-well-funded-than-ever-before-in-world-history/#comments Thu, 10 Aug 2023 21:44:58 +0000 https://americanconservativemovement.com/?p=195659 Back in 1974, the U.S. government and other multinational interests grew concerned about worldwide population growth and how it implicates U.S. security and overseas interests. The declassified Kissinger Report unveils high-level, diabolical plans for population control and uncovers the government’s sinister intent for depopulation efforts in the U.S. and abroad.

This grisly gambit of controlling populations and exterminating people en masse was discussed by Dr. Robert Malone in a recent speech at the 2023 White Coat Summit. At the summit, Malone was asked about the so-called covid-19 vaccines: “Why would a government wish to advance this technology?” As one of the pioneers of the mRNA technology, Malone concludes that the mRNA injections were developed by the Central Intelligence Agency (CIA) and the Defense Advanced Research Projects Agency (DARPA) through a front (Moderna) as part of a global depopulation program.

Practically every government action during the covid-19 crisis was designed for depopulation, especially the mRNA “vaccines”

Practically every high-level government action taken during the covid-19 crisis inflicted more harm, mental suffering, and death. Every coordinated propaganda campaign was scripted bio-terror that enabled a medical police state and a censorship regime that misled and herded people into a state of perpetual suffering, separation, and abuse.

Blind obedience to propaganda and unlawful mandates deepened the abuse and emboldened a ruthless and unaccountable vaccine industry. The false savior of government safety protocols and “lifesaving” vaccines masquerade today, even after killing untold numbers of people.

The restrictions against healthy people, the takedown of doctors who provided efficacious treatments for infectious disease, and the blackout against information on maintaining healthy immune function all pointed to the sinister conclusion: in every which way, populations were being targeted for extermination.

It was all part of a psychopathic plot to break our wills, to tear apart our families, and to strip us of our individuality, body autonomy and dignity. Resistance to every oppressive decree was necessary in order to escape the death throes of this monolithic evil.

The U.S. government enacted outrageous policies and emergency orders that suspended the Bill of Rights. The government aggressively funded this gargantuan evil with mandates of coercion and force. As Dr. Malone points out, all of the sciences — from molecular biology and biochemistry to virology and microbiology —  have been weaponized by the US government over the years and aimed toward the development of biowarfare programs.

Dr. Malone points out that Operation Paperclip imported both Nazi and Japanese biowarfare specialists decades ago. Instead of researching, publishing, and promoting information on the antiviral, antibacterial and immune-modulating properties of various phytochemicals that are abundant all around us, the National Institutes of Health (NIH) has been funding biolabs to weaponize viruses and bacteria to exploit human immune systems. Our own institutions have systemically weaponized science to depopulate us and profit from our suffering along the way, with new vaccine technologies that further mutate pathogens and exploit and weaken the innate function of our immune defenses.

Global institutions are well-funded and coordinate deadly propaganda campaigns that unleash mass terror and a medical police state

Global institutions now carry out these depopulation agendas and synchronize their propaganda campaigns to maximize compliance. The propaganda is designed to incite terror and fear in the global population, to create what Dr. Malone calls “mass formation psychosis.” From the World Health Organization to the World Economic Forum to the Bill and Melinda Gates Foundation, these multinational interests all coordinate their messages to promote bio-terror and to instill mass obedience to a global medical police state.

These organizations can be best described as the “specialized agencies” that were commissioned in the Kissinger Report to carry out “a global population strategy.” This global population strategy entails “functional assistance programs to create conditions for fertility decline” and encourages the United Nations, the specialized agencies, and private organizations to enact “population programs that assist in fertility decline around the globe.”

As we go about our lives and careers, we have to discern the propaganda that enables psychopaths to continue on with their population control schemes; we must be aware of our relationship to these sinister agendas, and we must decide how we will resist participation in these wicked schemes and change the course of this decades-long, well-coordinated strategy to depopulate the Earth.

Sources include:

]]> https://americanconservativemovement.com/the-global-depopulation-agenda-is-more-organized-and-well-funded-than-ever-before-in-world-history/feed/ 1 195659 Miscarriages and Stillbirths Due to “Vaccines” Up 5,271% in 2021 Compared to 2020 https://americanconservativemovement.com/miscarriages-and-stillbirths-due-to-vaccines-up-5271-in-2021-compared-to-2020/ https://americanconservativemovement.com/miscarriages-and-stillbirths-due-to-vaccines-up-5271-in-2021-compared-to-2020/#respond Thu, 29 Jun 2023 19:03:42 +0000 https://americanconservativemovement.com/?p=194133 “Pregnant women should get vaxxed,” they said.

The Covid-19 “vaccines” have proven to be the most dangerous and falsely promoted government-backed drugs in the history of mankind. The death tolls continue to rise, and despite unambiguous evidence that they’re neither safe nor effective, they’re still being heavily promoted as such. Corporate media, academia, and most in the medical community are either too scared or too complicit to report the truth.

Even as it seems to many that medical tyranny is waning and Pandemic Panic Theater is in its final act, the need to share information about the jabs has increased. Complacent people are gullible people. We expect another round of… something… to be launched any time between now and Election Day, 2024. That’s why data like this is so important to share:

It doesn’t take a mathematician to notice the sharp increase in stillbirths and miscarriages that took place in 2021. Over 5,100 have been reported since the Covid jabs were unleashed on the public. In 2020, there were 65, according to the CDC’s own data.

Any doctor, politician, academic, or journalist who used their status of influence to compel pregnant women to get jabbed is complicit in deaths of these preborn children. And if 5,100 have been reported, that means between 51,000 and 510,000 have actually died needlessly.

]]> https://americanconservativemovement.com/miscarriages-and-stillbirths-due-to-vaccines-up-5271-in-2021-compared-to-2020/feed/ 0 194133 “Reprehensible” FDA Sued for Withholding Covid-19 Vaxx Safety Analyses: “The Courts Will Command the FDA to Do Its Job” https://americanconservativemovement.com/reprehensible-fda-sued-for-withholding-covid-19-vaxx-safety-analyses-the-courts-will-command-the-fda-to-do-its-job/ https://americanconservativemovement.com/reprehensible-fda-sued-for-withholding-covid-19-vaxx-safety-analyses-the-courts-will-command-the-fda-to-do-its-job/#respond Sat, 28 Jan 2023 23:27:39 +0000 https://americanconservativemovement.com/?p=189528 The U.S. Food and Drug Administration (FDA) has been sued for withholding the results of key COVID-19 vaccine safety analyses.

The FDA’s actions violate federal law, the new lawsuit, filed on Jan. 26 in federal court in Washington by the nonprofit Children’s Health Defense (CHD), alleges.

The suit is seeking the raw results from the FDA’s analyses of reports to the Vaccine Adverse Event Reporting System (VAERS).

The system, which the FDA runs with the U.S. Centers for Disease Control and Prevention, accepts reports of post-vaccination adverse events.

As part of its vaccine safety monitoring, the FDA pledged to run a type of analyses called Empirical Bayesian (EB) data mining on the reports to see if any safety signals were triggered. Signals give agencies an idea of which problems may be caused by vaccines. Agencies are supposed to research signals to verify them or rule them unrelated to vaccination.

“A report to VAERS does not mean that a vaccine caused an adverse event. But VAERS can give CDC and FDA important information. If it looks as though a vaccine might be causing a problem, FDA and CDC will investigate further and take action if needed,” the CDC says on its website.

The FDA denied CHD’s request for the results of the data mining, claiming the records are “intra-agency memoranda consisting of opinions, recommendations, and policy discussions within the deliberative process of FDA, from which factual information is not reasonably segregable.”

The FDA also claimed the sought-after information “contains a discussion of legal and policy matters and fall within the attorney work product and attorney-client privileges as enunciated by the Supreme Court.”

The FDA also refused to provide the results of the EB data mining to The Epoch Times, using the same rationale.

In a set of operating procedures, the federal government said the FDA would carry out Empirical Bayesian data mining and the CDC would conduct a separate type of analyses using a method called Proportional Rate Ratio, or another way to analyze the VAERS data.

 

 

After lying about when it started the proportional data mining and stonewalling inquiries, the CDC recently released the results of the analyses to The Epoch Times, revealing the agency identified hundreds of adverse events potentially connected to the Pfizer and Moderna COVID-19 vaccines.

Kim Witczak, co-founder of Woodymatters, a nonprofit that advocates for a stronger FDA and drug safety system, said at the time that the agency’s refusal to provide the analyses was not acceptable.

“The secrecy is unacceptable for an agency that said it is transparent with the public about vaccine safety,” Witczak said.

Lawmakers, including Rep. Ronny Jackson (R-Texas), have also questioned (pdf) why the records were not released.

The FDA and CDC only publicly acknowledge a small number of adverse events as being definitely caused by or potentially caused by the messenger RNA shots, including myocarditis, or heart inflammation.

The CDC claimed that the results of its analyses “were generally consistent with EB data mining.”

CHD says the refusal by the FDA to release the EB mining results violates the Freedom of Information Act, which enables people and organizations to request information from federal agencies.

While exemptions exist, the FDA improperly withheld the requested data, the new lawsuit charges. It notes that the FDA did not provide any evidence to support its claims that it could not release the records.

While the CHD appealed to the government for a fresh look at the request, the FDA said it would not have a response to the appeal until “around” the summer of 2023.

The Freedom of Information Act requires an agency to make requested records “promptly available” to a requester and imposes other time restrictions, which have not been adhered to, the suit says.

CHD is asking the court to find the FDA’s failures to meet the time requirements unlawful and order the FDA to produce all non-exempt records within 20 days. CHD is also asking the court to award attorneys’ fees and other litigation costs. The FDA did not respond to a request for comment.

“It is long overdue for the FDA to release the data on the Empirical Bayesian data mining that it promised even before the COVID shot rollout” Mary Holland, president and general counsel of CHD, said in a statement. “It is reprehensible for this agency, established to protect the American people, to conceal critical data. I trust that the courts will command the FDA to do its job.”

Article cross-posted from our premium news partners at The Epoch Times. Image by Felton Davis via Flickr, CC BY 2.0.

]]> https://americanconservativemovement.com/reprehensible-fda-sued-for-withholding-covid-19-vaxx-safety-analyses-the-courts-will-command-the-fda-to-do-its-job/feed/ 0 189528 45 Deaths, 5,000+ Adverse Events Following Updated Booster Shots Reported to VAERS, CDC Data Show https://americanconservativemovement.com/45-deaths-5000-adverse-events-following-updated-booster-shots-reported-to-vaers-cdc-data-show/ https://americanconservativemovement.com/45-deaths-5000-adverse-events-following-updated-booster-shots-reported-to-vaers-cdc-data-show/#respond Sat, 29 Oct 2022 09:11:12 +0000 https://americanconservativemovement.com/?p=184060

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website.

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,447,520 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and Oct. 21, 2022, to the Vaccine Adverse Event Reporting System (VAERS).

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S. The data included a total of 31,696 reports of deaths and 263,462 serious injuries, including deaths, during the same time period.

There were a total of 5,435 reports of adverse events following the new COVID-19 bivalent booster as of Oct. 21, 2022. The data included a total of 45 deaths and 280 serious injuries. As of Oct. 27, 22.8 million people have received the updated bivalent booster dose.

Of the 31,696 reported deaths, 20,252 cases are attributed to Pfizer’s COVID-19 vaccine, 8,599 cases to Moderna, 2,752 cases to Johnson & Johnson (J&J) and no cases yet reported for Novavax.

Excluding “foreign reports” to VAERS, 887,564 adverse events, including 14,920 deaths and 92,482 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Oct. 21, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 14,920 deaths reported as of Oct. 21, 7% occurred within 24 hours of vaccination and 15% occurred within 48 hours of vaccination.

In the U.S., 632 million COVID-19 vaccine doses had been administered as of Oct. 19, including 376 million doses of Pfizer, 238 million doses of Moderna and 19 million doses of J&J.

Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed. Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

VAERS data from Dec. 14, 2020, to Oct. 21, 2022, for 6-month-olds to 5-year-olds show:

VAERS data from Dec. 14, 2020, to Oct. 21, 2022, for 5- to 11-year-olds show:

VAERS data from Dec. 14, 2020, to Oct. 21, 2022, for 12- to 17-year-olds show:

According to the CDC, “VAERS data available to the public include only the initial report data to VAERS. Updated data which contains data from medical records and corrections reported during follow up are used by the government for analysis. However, for numerous reasons including data consistency, these amended data are not available to the public.”

  • 269 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death.
  • 1,336 reports of myocarditis and pericarditis with 1,167 cases attributed to Pfizer’s vaccine.
  • 301 reports of blood clotting disorders with 278 cases attributed to Pfizer.
  • 27 cases of postural orthostatic tachycardia syndrome (POTS) with all cases attributed to Pfizer’s vaccine.

VAERS data from Dec. 14, 2020, to Oct. 21, 2022, for all age groups combined, show:

Children’s Health Defense (CHD) asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

CDC pressured FDA to authorize COVID boosters without clinical trials

The CDC pressured U.S. regulators to clear COVID-19 boosters without clinical trial data, according to emails obtained by Judicial Watch.

CDC officials relayed to counterparts at the FDA in early August 2021 that they wanted authorization for Moderna and Pfizer boosters, as data began showing that the vaccines weren’t working as well as initially promoted.

The conversation took place on a call that was described by Dr. Phil Krause, a top FDA official, to several other FDA workers. On that call, the CDC “evidently stated” they would assemble all the data they were aware of on third dosing in the immunocompromised setting and send it to the FDA in hopes they would authorize a third dose for those with compromised immune systems under Emergency Use Authorization.

All COVID-19 vaccines were authorized only for emergency use at that time. No boosters had been authorized and no clinical data were available for a third vaccine dose. Less than two weeks later, the FDA authorized boosters for certain people, including immunocompromised persons.

The agency said “a thorough review of the available data” concluded the group “may benefit” from a third dose. The only data cited on efficacy were from two studies, one conducted by French researchers and another by Canadian researchers. Pfizer and Moderna hadn’t completed any clinical trials.

FDA slow-walked studies on COVID vaccine safety signals in elderly

The FDA took more than a year to follow up on a potential increase in serious adverse events in elderly people who received Pfizer’s COVID-19 vaccine, according to an investigative report published Tuesday by The BMJ.

According to The BMJ, in July 2021, the FDA “quietly disclosed” the findings of a potential increase in four types of serious adverse events in elderly people who had received a Pfizer COVID-19 vaccine: acute myocardial infarction, disseminated intravascular coagulation, immune thrombocytopenia, and pulmonary embolism.

The FDA disclosure lacked specific details, such as the magnitude of the increased potential risk, and the agency said it would “share further updates and information with the public as they become available.”

The FDA did not alert physicians or the public, via a press release or any other means, The BMJ investigator said.

Eighteen days later, the FDA published a study planning document that outlined a protocol for a follow-up epidemiological study for investigating the matter more thoroughly.

According to the BMJ, the recondite technical document disclosed the unadjusted risk ratio estimates originally found for the four serious adverse events, which ranged from 42% to 91% increased risk.

More than a year later, the status and results of the follow-up study are unknown. The BMJ report also alleged the FDA has not “publicly acknowledged other published observational studies or clinical trial reanalyses reporting compatible results.”

CDC knew COVID shots could cause myocarditis in young males months before telling the public

Two months after COVID-19 vaccines were rolled out to the U.S. public, a statistically significant vaccine safety signal for myocarditis in males ages 8 to 21 appeared in the CDC’s VAERS database, but CDC officials waited another three months before alerting the public, according to a new study.

The study, “Delayed Vigilance: A Comment on Myocarditis in Association with the COVID-19 Injections,” by Karl Jablonowski, Ph.D., and Brian Hooker, Ph.D., P.E., was published on Oct. 17 in the International Journal of Vaccine Theory, Practice, and Research.

In their study, Jablonowski and Hooker recorded and analyzed the increasing incidence of myocarditis as it progressively became a statistically significant “signal” in VAERS.

In an interview with The Defender, Hooker said the paper shows a “strong, statistically significant vaccine adverse event ‘signal’ for myocarditis in males 8 to 21 years of age was seen on the VAERS database as early as Feb. 19, 2021, just two months after the release of the COVID-19 vaccine to the U.S. public.”

Yet, instead of sounding the alarm, “CDC officials buried the connection between COVID-19 vaccination and myocarditis until May 27, 2021,” Hooker added. “By this date, over 50% of the eligible U.S. population had received at least one mRNA COVID-19 vaccine.”

All age groups at higher risk of myocarditis death after COVID vaccines

People of all ages are at higher risk of death from heart inflammation after COVID-19 vaccination compared with the typical occurrence of myocarditis death, according to a new preprint study.

Researchers in Japan analyzed deaths caused by myocarditis, a form of heart inflammation, where the myocarditis set in within 28 days of vaccination. Thirty-eight deaths fit the definition, about half of which were diagnosed by autopsy and or biopsy, with the others being determined through tools such as blood tests and electrocardiograms.

Researchers then took the vaccinated mortality rate and compared it with the death from myocarditis rate from the general population before the pandemic, in the years 2017 to 2019.

Using data provided by the Japanese government, the researchers observed an increased myocarditis mortality rate ratio in the SARS-CoV-2 vaccinated population compared with the general population during the three years pre-COVID-19 pandemic era, especially in young adults.

An increased risk was also observed in the middle-aged (40s) and elderly vaccinated populations.

Even estimating the lowest level of the effect, the risk of COVID-19 vaccination on myocarditis death would be at least four times higher than the unadjusted mortality risk, the researchers said. There are also signs that some post-vaccination deaths aren’t reported properly, they added.

Recent studies identify new concerns related to COVID vaccines and organ transplants

Recent studies identified a new concern related to the failure of transplanted kidneys and other organs: COVID-19 vaccination.

In one study, published in September in Transplant Infectious Disease, researchers cataloged acute organ rejection within a week or two of COVID-19 vaccination in five individuals who had received kidney, liver or heart transplants six to 18 months earlier.

In August, Japanese researchers reported rejection of corneal grafts — which ordinarily have a high success rate — in COVID-19 vaccine recipients, occurring from one day to six weeks post-vaccination.

Noting literature that documents transplant rejection in association with other vaccines such as influenza, hepatitis B, tetanus and yellow fever, the Japanese authors expressed worry about what “the projected societal shift towards a more frequent vaccination schedule” portends for transplant recipients.

Concerns about the impact of COVID-19 jabs on people with existing transplants are important, but another pressing-yet-unaddressed issue is what happens when an unvaccinated person receives a transplanted organ from someone who received a COVID-19 vaccination.

Woman injured by Gardasil vaccine shares how COVID shots injured her mother and ended the life of her grandmother

In 2012, when she was 20 years old, Rochelle was so injured by Merck’s Gardasil vaccine that she had to give up her pre-med studies.

Ten years later, her mother was injured by Moderna’s COVID-19 vaccine, and shortly after, her grandmother died just a few weeks after getting her second dose of Pfizer’s vaccine.

In an exclusive interview with The Defender, Rochelle, now 30, shared her story, and her mother and grandmother’s stories. Rochelle told The Defender that her father, grandfather and brother all became doctors, and her mother, Marcia, was a nurse.

Rochelle’s mother received both doses of the Moderna vaccine in the spring of 2021. Adverse events followed soon after the first dose and she was diagnosed with polymyalgia rheumatica (PMR), which her doctor said was induced by the vaccine.

Marcia’s PMR “caused severe inflammation throughout her body,” leading to “spontaneous tendon ruptures and a lower back disc herniation,” said Rochelle. In addition, “she tore her thumb tendon just by moving her hand normally and required urgent surgery to repair it.”

Rochelle said her mother will need several surgeries for complete tendon tears in her shoulder, and may potentially need spine surgery to repair her herniated disc. She is also on medication and for a long time, could not perform basic tasks.

What happened to Rochelle after getting the Gardasil human papillomavirus, or HPV, vaccine, and her mother, Marcia, after getting the COVID-19 vaccine was bad enough — but not as bad as what happened to Rochelle’s grandmother. After receiving her second Pfizer vaccine, Jean lost her ability to communicate, her health declined severely and within a few weeks, she was dead.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

]]> https://americanconservativemovement.com/45-deaths-5000-adverse-events-following-updated-booster-shots-reported-to-vaers-cdc-data-show/feed/ 0 184060 CDC Drops Quarantine, Distancing Recommendations, as 1.3 Million Covid “Vaccine” Injuries Reported to VAERS https://americanconservativemovement.com/cdc-drops-quarantine-distancing-recommendations-as-1-3-million-covid-vaccine-injuries-reported-to-vaers/ https://americanconservativemovement.com/cdc-drops-quarantine-distancing-recommendations-as-1-3-million-covid-vaccine-injuries-reported-to-vaers/#comments Sat, 13 Aug 2022 11:20:21 +0000 https://americanconservativemovement.com/?p=178323 Editor’s note: In previous VAERS weekly updates, The Defender focused exclusively on U.S. reports in the sections where reports are broken out by age groups and types of adverse events. However, excluding foreign reports from these categories excludes thousands of vaccine injuries reported to the system, so those sections now include all — U.S. and foreign combined — reports submitted to VAERS in the categories indicated.

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,379,438 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and Aug. 5, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 7,964 adverse events over the previous week.

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 30,162 reports of deaths — an increase of 181 over the previous week — and 251,075 serious injuries, including deaths, during the same time period — up 1,959 compared with the previous week.

Of the 30,162 reported deaths, 19,462 cases are attributed to Pfizer’s COVID-19 vaccine, 8,038 cases to Moderna, 2,613 cases to Johnson & Johnson (J&J) and no cases yet reported for Novavax.

Excluding “foreign reports” to VAERS, 854,084 adverse events, including 13,972 deaths and 87,488 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Aug. 5, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 13,972 U.S. deaths reported as of Aug. 5, 7% occurred within 24 hours of vaccination, 15% occurred within 48 hours of vaccination and 54% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 604 million COVID-19 vaccine doses had been administered as of Aug. 3, including 357 million doses of Pfizer, 228 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).

Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.

Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

VAERS data from Dec. 14, 2020, to Aug. 5, 2022, for 6-month-olds to 5-year-olds show:

VAERS data from Dec. 14, 2020, to Aug. 5, 2022, for 5- to 11-year-olds show:

VAERS data from Dec. 14, 2020, to Aug. 5, 2022, for 12- to 17-year-olds show:

  • 32,945 adverse events, including 4,189 rated as serious and 118 reported deaths.
    According to the CDC, “VAERS data available to the public include only the initial report data to VAERS. Updated data which contains data from medical records and corrections reported during follow up are used by the government for analysis. However, for numerous reasons including data consistency, these amended data are not available to the public.”
  • 268 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 94% of cases attributed to Pfizer’s vaccine.
  • 1,304 reports of myocarditis and pericarditis with 650 cases attributed to Pfizer’s vaccine.
  • 298 reports of blood clotting disorders with 275 cases attributed to Pfizer.
  • 26 cases of postural orthostatic tachycardia syndrome (POTS) with all cases attributed to Pfizer’s vaccine.

VAERS data from Dec. 14, 2020, to Aug. 5, 2022, for all age groups combined, show:

Children’s Health Defense (CHD) asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

New CDC COVID guidance ditches distinctions between vaccinated and unvaccinated

The CDC on Thursday issued sweeping new recommendations as part of the agency’s efforts to overhaul its COVID-19 guidance.

“This guidance acknowledges that the pandemic is not over, but also helps us move to a point where COVID-19 no longer severely disrupts our daily lives,” the CDC’s Greta Massetti said in a press release.

Here are the biggest changes to the CDC’s guidance:

  • Unvaccinated people now have the same guidance as vaccinated people.
  • Those who are exposed to the virus are no longer required to quarantine regardless of vaccination status.
  • Students may stay in class even if they’ve been exposed to COVID-19.
  • Six-foot social distancing is no longer recommended.
  • Contact tracing and routine surveillance testing of symptomatic people are no longer recommended in most settings.

According to The New York Times, the CDC has been working for months on the new guidance which builds on previous guidance issued in February that reduced isolation times for those who get COVID-19.

The agency said it is making changes to its guidance now because “vaccination and prior infections have granted many Americans some degree of protection against the virus, and treatments, vaccines and boosters are available to reduce the risk of severe illness.”

According to The National Law Review:

“The CDC’s focus on individual responsibility, the removal of distinctions between vaccinated and unvaccinated, the removal of quarantine recommendations and the discussion of mask wearing as an individual responsibility are good news for employers who are considering relaxing COVID-19 workplace requirements.

“This likely will not be the last we hear from the CDC on this topic. Indeed, the CDC stated that it intends to issue more specific guidance for settings such as healthcare, congregate living, and travel.”

Pfizer vaccine efficacy in teens wanes 27 days after second dose

A study published Aug. 8 in The Lancet showed the effectiveness of the Pfizer-BioNTech COVID-19 vaccine against symptomatic infection among adolescents “rapidly declined over time,” waning from just 27 days after the second dose.

Researchers analyzed data from 503,776 COVID-19 tests of 2,948,538 adolescents — ages 12-17 — in Brazil from Sept. 2, 2021, to April 19, 2022, and 127,168 tests of 404,673 adolescents in Scotland from Aug. 6, 2021, to April 19, 2022.

The study showed vaccine efficacy began to decline 27 days after the second dose for both countries, plummeting to 5.9% (95% CI 2.2–9.4) in Brazil and dropping to 50.6% (95% CI 42.7–57.4) in Scotland at 98 days after adolescents received the second dose.

While protection against symptomatic COVID-19 dropped dramatically in both countries less than one month after the second dose, protection against severe illness — defined as hospitalization or death within 28 days — remained above 80% in Brazil from 28 days to 98 days and beyond.

The authors sought to assess protection against severe illness in Scotland but were unable to do so because so few cases of severe COVID-19 in adolescents in Scotland were reported during the time of the study.

The authors concluded that “two doses are insufficient to sustain protection against symptomatic disease” in adolescents and recommended more research be done on the need for booster doses.

‘Stunning’ link between Pfizer vaccine and myocarditis in teens, study shows

A preprint study conducted during Thailand’s national COVID-19 vaccination campaign showed what one physician described as a “stunning” association between myocarditis and the Pfizer-BioNTech vaccine.

The study analyzed 301 participants ages 13-18 who were healthy and without abnormal symptoms after receiving their first vaccine dose. Participants with a history of cardiomyopathy, tuberculous pericarditis or constrictive pericarditis and severe allergic reaction to the COVID-19 vaccine were excluded from the study.

Researchers found that 18% of the 301 teens analyzed had an abnormal electrocardiogram, or EKG after receiving their second dose of Pfizer, 3.5% of males developed myopericarditis or subclinical myocarditis, two were hospitalized and one was admitted to the ICU for heart problems.

Cardiovascular adverse events observed during the study included tachycardia (7.64%), shortness of breath (6.64%), palpitation (4.32%), chest pain (4.32%) and hypertension (3.99%).

Fifty-four adolescents had abnormal electrocardiograms after vaccination, three patients had minimal pericardial effusion with findings compatible with subacute myopericarditis and six patients experienced mitral valve prolapse.

All patients were male and had abnormal electrocardiograms, particularly sinus tachycardia. Researchers said the clinical course was mild in all cases.

Military using ‘Comirnaty’ vaccine produced at facility not approved by FDA

In an exclusive interview with The Defender, a U.S. Coast Guard (USCG) service member alleged the U.S. Department of Defense (DOD) is administering COVID-19 vaccines from vials of Pfizer’s Comirnaty-labeled vaccines that are not produced in a facility approved by the FDA.

Lt. Chad R. Coppin, in a July 30 declaration submitted to Sen. Ron Johnson (R-Wis.) under penalty of perjury, detailed his personal investigation into the availability and origin of Comirnaty-labeled COVID-19 vaccine vials at U.S. military facilities.

Coppin relayed his concerns in an interview with The Defender, as did Holly Freincle, the wife of a U.S. military service member stationed at Fort Detrick, Maryland, who corroborated Coppin’s claims that Comirnaty-labeled vaccine vials are appearing at military service facilities.

Until now, the DOD has claimed the Pfizer-BioNTech COVID-19 vaccine, administered under Emergency Use Authorization, is “interchangeable” with the fully licensed Pfizer Comirnaty vaccine — which until recently, was said to be unavailable at military facilities.

In his July 30 declaration, Coppin, who has served with the USCG since March 2002, reported that after a long period of unavailability, the “Comirnaty” vaccine began to appear at U.S. military facilities in June.

© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

]]> https://americanconservativemovement.com/cdc-drops-quarantine-distancing-recommendations-as-1-3-million-covid-vaccine-injuries-reported-to-vaers/feed/ 1 178323 9-Year-Old With No Pre-Existing Conditions Died 2 Weeks After Pfizer Shot, Latest VAERS Data Show https://americanconservativemovement.com/9-year-old-with-no-pre-existing-conditions-died-2-weeks-after-pfizer-shot-latest-vaers-data-show/ https://americanconservativemovement.com/9-year-old-with-no-pre-existing-conditions-died-2-weeks-after-pfizer-shot-latest-vaers-data-show/#comments Fri, 29 Jul 2022 22:42:45 +0000 https://americanconservativemovement.com/?p=177370 The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,357,940 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and July 22, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 6,990 adverse events over the previous week.

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 29,790 reports of deaths — an increase of 155 over the previous week — and 247,686 serious injuries, including deaths, during the same time period — up 1,010 compared with the previous week.

Of the 29,790 reported deaths, 19,236 cases are attributed to Pfizer’s COVID-19 vaccine, 7,917 cases to Moderna, 2,584 cases to Johnson & Johnson (J&J) and no cases yet reported for Novavax.

Excluding “foreign reports” to VAERS, 848,094 adverse events, including 13,805 deaths and 86,604 serious injuries, were reported in the U.S. between Dec. 14, 2020, and July 22, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 13,805 U.S. deaths reported as of July 22, 7% occurred within 24 hours of vaccination, 15% occurred within 48 hours of vaccination and 54% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 601 million COVID-19 vaccine doses had been administered as of July 20, including 355 million doses of Pfizer, 227 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).

Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.

Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

U.S. VAERS data from Dec. 14, 2020, to July 22, 2022, for 6-month-olds to 5-year-olds show:

U.S. VAERS data from Dec. 14, 2020, to July 22, 2022, for 5- to 11-year-olds show:

  • 12,232 adverse events, including 313 rated as serious and 9 reported deaths.
    The most recent reported death involves a 9-year-old girl (VAERS I.D. 2377304) from California who died two weeks after receiving her first dose of Pfizer’s COVID-19 vaccine. The child experienced abdominal pain, sore throat and chest pain during the 2-3 days before she died, according to the VAERS report, which did not indicate any pre-existing conditions.
  • 24 reports of myocarditis and pericarditis.
  • 47 reports of blood clotting disorders.
  • 101 reports of seizures.

U.S. VAERS data from Dec. 14, 2020, to July 22, 2022, for 12- to 17-year-olds show:

U.S. VAERS data from Dec. 14, 2020, to July 22, 2022, for all age groups combined, show:

Children’s Health Defense (CHD) asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

Woman develops rare acute kidney failure after first Pfizer dose

A woman developed a rare case of acute kidney renal failure — linked to antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) — a few days after receiving her first dose of Pfizer-BioNTech’s COVID-19 vaccine.

According to a case study published July 18 in Nephron, a previously healthy 47-year-old woman presented to a primary care clinic for bilateral flank pain, generalized weakness and bilateral lower extremity swelling that started three days after her first Pfizer shot.

AAV is a group of diseases characterized by the destruction and inflammation of small vessels. The condition occurs when neutrophils attack small and medium vessels of the body, which can affect several organs, such as the kidney, stomach, intestine and lungs.

This case adds to previous reports suggesting COVID-19 vaccines may, in rare instances, promote the development or worsening of autoimmune diseases, such as AAV, from their silent state, according to Patricia Inacio, Ph.D., who summarized the report for ANCA Vasculitis News.

“Rarely, autoimmune processes have been described post-vaccination. AAV is an example of an autoimmune disease that can be induced or flared up from a silent state by COVID-19 vaccines,” the authors concluded. “A high index of suspicion regarding the presence of an autoimmune renal process is needed whenever a recently COVID-19-vaccinated individual presents for acute kidney injury.”

43% of parents ‘definitely’ won’t vaccinate young kids for COVID

According to survey results released Tuesday, 43% of U.S. parents of children under 5 will “definitely not” give their child a COVID-19 vaccine amid concerns the vaccine poses a greater risk to kids than the virus.

The survey, published by the Kaiser Family Foundation, found that 27% of parents said they would “wait and see,” while another 13% said they would have their children vaccinated only if required to do so for school or childcare.

Even parents who were vaccinated against COVID-19 said they would not give permission for their youngest children to get vaccinated.

When asked why they will not vaccinate their eligible child under 5 “right away,” parents cited “concerns about the newness of the vaccine and not enough testing or research, concerns over side effects and worries over the overall safety of the vaccines.”

CDC used flawed data to justify authorizing COVID-19 vaccines for kids

A CDC official used data from a flawed preprint study that exaggerated the risk of death for children from COVID-19 in her presentations to CDC and FDA advisors who were responsible for recommending Pfizer and Moderna’s vaccines for infants and young children.

The study, first published May 25 on the medRxiv preprint server, was authored by a group of U.K. researchers. On June 28, the authors published a revised version of the study, after critics questioned some of their original findings.

“It’s really disturbing that data this poor made its way into the meetings to discuss childhood COVID and that it took me less than a few minutes to find a major flaw (and then I found many more as I looked deeper),” said Kelley K, who was the first to point out some of the study’s flaws on her website COVID-Georgia.com.

After learning of Kelley’s analysis, The Defender reviewed the original preprint, confirmed Kelley’s findings and uncovered additional flaws in the original preprint and also in the June 28 revised version.

CHD demands D.C. schools rescind COVID vaccine mandate

Robert F. Kennedy, Jr., chairman and chief legal counsel for CHD, in a letter to the superintendent of the District of Columbia school system threatened to sue the school district unless it rescinds its recently announced COVID-19 vaccine mandate for students ages 12 and up.

State Superintendent of Education Christina Grant announced on July 19 that student immunization requirements for the upcoming 2022-2023 school year will include the COVID-19 vaccine for all students who are of an age for which there is a vaccine fully approved by the FDA now that the FDA has fully approved the Pfizer-BioNTech vaccine for individuals 12 to 15 years old.

D.C. law requires students in all area schools, including private, parochial and independent schools, to be fully compliant with mandated vaccinations, unless they have an approved exemption. The law also requires schools to verify immunization certification for all students.

The requirement was detailed in a law the D.C. Council approved last year and is the first legislation of its kind in the region.

Although courts have upheld many childhood vaccination requirements for licensed and approved vaccines, no court has ever upheld a mandate for schoolchildren for an Emergency Use Authorization vaccine, according to Kennedy.

© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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