Despite the Fact that 70% of All Australians are "Fully Boosted,” Deaths from COVID Have Reached a Record High. Contrary to Media Lies the COVID Injected are Dying at an Ever-Increasing Rate
/From [HERE] The latest figures are in, and things are not looking good for “fully vaccinated” Australia.
Even though more than 96 percent of the native population there took the first two mRNA (messenger RNA) jabs for the Wuhan coronavirus (Covid-19), and more than 70 percent are fully “boosted,” Chinese Virus deaths throughout the country have reached a record high.
The following data chart clearly shows that ever since the launch of Operation Warp Speed, injection-related deaths Down Under have been soaring. As of this writing, a peak has formed to suggest that with the passage of time, the fully injected are dropping dead at an ever-increasing rate.
Had Australia opted for ivermectin and hydroxychloroquine (HCQ) instead of Fauci Flu shots, the plandemic would have ended ages ago. Instead, Australia is now seeing mass death rather than a recovery. (Related: Australian officials want Aussies to get injected a bi-annual intervals for the rest of time.)
In fact, there were almost no covid-related deaths at all in Australia prior to the launch of the “vaccines.” There was a small peak in the fall of 2020 followed by a precipitous drop back to baselines levels, followed by a massive peak once people started getting injected.
Interestingly, the booster shot campaign was followed by another massive spike and peak, which will more than likely be followed by continued increases in the death count as antibody-dependent enhancement (ADE) and other jab-induced health conditions take their toll.
“We were warned, but only intelligent people listened,” wrote a commenter in response to the news. “Antibody-dependent enhancement is happening, it is real, and it destroys the immune system.”
“No one mistreated their citizens more than Australia during the crisis,” added another. “The people that did that should be in jail.”
This is now a plandemic of the fully vaccinated
New South Wales (NSW) is reportedly seeing the most new “cases” of the Wuhan Flu, followed by Queensland and Victoria.
Each of these areas, as you may recall, imposed heavy restrictions throughout the plandemic – restrictions that area residents were told would put an end to the virus.
“Quarantine” concentration camps were set up; people were forced to mask everywhere they went; and public movement was restricted – but to no avail. The Chinese Virus is here to stay, thanks to the injections.
The media would have us all believe that people are “catching” and “re-catching” covid over and over again, but the reality is that what we are now seeing is a plandemic of the fully vaccinated whose immune systems are shot.
“They’re exhibiting symptoms of poisoning,” wrote another commenter about what the fully jabbed are experiencing, which is not “covid.” “Coughing and fever are mild symptoms. Neurological damage, spasms, and paralysis are serious symptoms, not unlike what happens to a cockroach that is sprayed with RAID.”
“Clots are a sign of internal bleeding. Severe clotting leads to amputation and heart attacks. The most severe symptom? Death.”
Another pointed out that nobody who is unvaccinated is experiencing any of this, which further proves that what sick people are suffering from is vaccine damage, not covid infection.
“Fake immunity designed to kill you never beats natural immunity,” wrote someone else about how the so-called vaccines do not in any way produce real or lasting immunity, but instead provoke vaccine-induced AIDS (VAIDS).
“The unvaxxed are not getting sick not because they have natural immunity to a non-existent pathogen, but because they haven’t been poisoned,” added someone else. “The mRNA drug causes epithelial cells to manufacture the toxic spike protein 24/7, 365. There’s no off switch.”
Novel Lawsuit Claims COVID 'Shelter in Place' or Shut Down Orders Interfered with the Inalienable Right to Earn a Living and Arbitrarily Denied Fruits of Labor Under NC Law
/Shelter in place orders were unnecessary Government seizures of people’s livelihoods and businesses that forced indefinite closures and widespread layoffs. Said conduct was not narrowly tailored because other ‘precautionary measures to manage contact tracing of [customers]; install plexiglass, touchless thermometers, six-feet distance markers, and screening booths; and to initiate vigilant cleaning procedures—all in consult with local health officials—would have been sufficient to combat the ALLEGED spread of COVID-19.’ (At any rate, asymptomatic transmission of COVID is epidemiologically irrelevant and shelter in place orders had no detectable impact on epidemic spreading, cases, hospitalisations, or deaths. Said governmental conduct was “among the most repressive acts ever imposed on citizens in a democracy.”) [MORE] The government’s actions may be described as “uncompensated takings” that violate the Takings Clause of the 5th Amendment. That is, the government is legally obligated to properly compensate citizens for their tangible losses. [MORE] If you believe such things as “rights” exist in the first place. The interesting lawsuit below is not a takings clause suit but invokes the NC Constitution.
From [HERE] Owners of an Alamance County speedway can move forward with a lawsuit against the state's top health official. The suit stems from a COVID-19 shutdown order.
Ace Speedway owners argue the shutdown deprived them of the right "to the enjoyment of the fruits of their own labor." They also contend the shutdown amounted to selective enforcement of a COVID-19 emergency order.
A unanimous decision from the N.C. Court of Appeals means the state Supreme Court faces no obligation to take the case.
A unanimous N.C. Court of Appeals panel has ruled that owners of an Alamance County racetrack shut down during the COVID-19 pandemic can move forward with a lawsuit against the state’s top health official.
Ace Speedway’s lawsuit argues that a shutdown order from Dr. Mandy Cohen, then serving as secretary of the N.C. Department of Health and Human Services, violated the speedway owners’ rights. The suit contends the shutdown infringed on speedway owners’ right to earn a living. The shutdown also represented selective enforcement of Gov. Roy Cooper’s COVID executive orders, according to the suit.
The suit is now known as Kinsley v. Ace Speedway Racing Ltd., with current DHHS Secretary Kody Kinsley replacing Cohen as the target of the speedway’s legal action.
“This case makes us consider the use of overwhelming power by the State against the individual liberties of its citizens and how that use of power may be challenged,” wrote Judge Jefferson Griffin.
“Ace’s counterclaims propose that the Governor’s orders were enforced upon them without justification and without equal protection of law,” Griffin added. “Ace’s counterclaims are constitutional claims alleging (1) executive orders issued by the Governor in response to the COVID-19 pandemic were an unlawful infringement on Ace’s right to earn a living as guaranteed by our Constitution’s fruits of labor clause, and (2) the Secretary’s enforcement actions against Ace under the executive order constituted unlawful selective enforcement.”
“We hold that Ace pled each of its constitutional claims sufficiently to survive the Secretary’s motion to dismiss.”
Ace held a series of auto races in May and June 2020, even after Cooper personally asked the Alamance County sheriff to urge the speedway to shut down. Cooper had issued a COVID-19 executive order blocking “mass gatherings” of more than 25 people.
Ace’s races drew at least 1,000 spectators and as many as 2,550 people. The speedway operated with COVID abatement measures adopted in consultation with local health officials.
Jason Turner, an Ace Speedway owner, also attracted media attention for his outspoken comments against the governor’s shutdown efforts.
Cohen issued an abatement order on June 8, 2020, and secured a court order forcing Ace to shut down its operations.
The speedway filed suit and continued its legal action, even after Cohen dropped her abatement efforts in September 2020, when Cooper had loosened some mass gathering restrictions. A trial judge ruled in January 2021 against the health secretary’s motion to dismiss Ace’s constitutional claims.
Griffin’s opinion focused attention on Ace’s argument that Cohen violated Article I, Section 1 of the N.C. Constitution. That section says North Carolinians’ “inalienable rights” include “the enjoyment of the fruits of their own labor.”
“[T]he addition of a right to the fruits of one’s labor to the North Carolina Constitution sought to increase the floor of protections granted by similar provisions in the United States federal constitution,” Griffin wrote. “Since then, our courts have construed North Carolina citizens’ right to the ‘fruits of their labor’ to be synonymous with their ‘right to earn a living’ in whatever occupation they desired.”
“The core principle behind the fruits of their labor clause is that government ‘“may not, under the guise of protecting the public interests, arbitrarily interfere with private business, or impose unusual and unnecessary restrictions upon lawful occupations,”’” Griffin wrote.
“The intended purpose of the Governor’s order was not to regulate a particular occupation or business enterprise, but the direct and intended purpose of the Abatement Order was to cease the operation of a business,” the judge added. “It cannot be denied that the scope and breadth of the Abatement Order restricted or otherwise interfered with the lawful operation of a business serving the public.”
“We hold that Ace adequately pled that the Secretary, through [the] Abatement Order, deprived Ace of its constitutional right to the fruits of one’s own labor and, therefore, sovereign immunity cannot bar Ace’s claim,” Griffin wrote.
Ace also “sufficiently pleads a constitutional challenge” that Cohen violated speedway owners’ rights under Article I, Section 19 of the N.C. Constitution. It reads that “no person shall be denied the equal protection of the laws.”
“Ace effectively pled that it was among a class of ‘many speedways’ that similarly conducted races with fans in attendance during the period where such actions were banned,” Griffin explained. “Ace further pled that Governor Cooper and the Secretary ‘singled out’ Ace for enforcement by directing the Sheriff to take action against Ace and, when that failed, by issuing the Abatement Order against Ace alone.”
“Finally, Ace’s complaint pled its belief that it was singled out for enforcement in response to Defendant Turner’s statements to the press ‘and not because a true Imminent Hazard exist[ed,]’ as the Secretary asserted in the Abatement Order,” Griffin added. “These pleadings, taken as true, sufficiently allege bad faith enforcement of [Cooper’s executive order] against Ace alone.”
Kinsley could appeal to the N.C. Supreme Court. Because Judges Jeff Carpenter and Fred Gore agreed with Griffin and ruled unanimously, the state’s highest court faces no obligation to take the case.
Without an appeal, the case would head back to Superior Court for a trial on the merits of Ace Speedway’s claims.
CHD Survey Finds that After Getting a COVID Shot 15% of US Adults Have Been Diagnosed with a New Health Condition - 21% of Blacks and 32% of Latinos
/From [CHD] More than two years after Operation Warp Speed began, Children’s Health Defense (CHD) commissioned John Zogby Strategies to conduct two surveys (see here and here) about attitudes and the overall health of American adults.
Key highlights from the survey of 1,038 adults
The survey found that 67% of respondents received one or more COVID-19 vaccines, while 33% are unvaccinated. Furthermore, among those vaccinated, 6% received one dose, 28% received two doses, 21% received three doses, and 12% took four or more.
Of those receiving a COVID-19 vaccine, 15% say they’ve been diagnosed by a medical practitioner with a new condition within a matter of weeks to several months after taking the vaccine.
“The fact that the Centers for Disease Control and Prevention (CDC) reports more than 232 million Americans ages 18-65 have taken at least one dose of the COVID-19 vaccine, and 15% of those surveyed report a newly diagnosed condition is concerning and needs further study,” said Children’s Health Defense (CHD) executive director Laura Bono. “The mRNA vaccine technology is new and clinical trials naturally have no long-term data. CHD believes this survey points to the need for further study.”
Other key demographics of newly diagnosed medical conditions after COVID-19 vaccines show:
17% of those receiving two doses
13% of respondents had three shots
30% of those ages 18-29
23% of those ages 30-49
6% of those ages 50-64
4% of those older than 65
7% of whites
21% of African-Americans
32% of Hispanics
15% of liberals
14% of moderates
8% of conservatives
A follow-up question provided a list of medical conditions and asked diagnosed respondents to “select all that apply.” Among those who were medically diagnosed with a new condition within a matter of weeks to several months, the top five cited conditions were:
21% blood clots
19% heart attack
18% liver damage
17% leg clots/lung clots
15% stroke
Overall, 67% reported that getting the vaccine was a good decision, 24% were neutral and 10% regret it.
Survey participants were then asked if someone they personally know had been medically diagnosed with a new medical condition within the same time frame. Overall, 26% reported yes, while 63% reported no.
Looking at age cohorts:
34% of those ages 18-29 say they know someone who was diagnosed, as did
30% of those ages 30-49,
21% of those ages 50-64,
and 18% of those older than 65
Again, respondents were offered the same list of conditions and asked to “select all that apply.” The top five cited conditions were:****
28 % blood clots
20% stroke
19% autoimmune
16% lung clots
15% heart attack
Key highlights from the survey of 829 adults ages 18-49
Among those under age 50 – 62% report receiving a COVID-19 vaccine vs. 38% who have had none.
Among those receiving any COVID-19 vaccine, almost one quarter — 22% — report being medically diagnosed within a matter of weeks to several months after taking a shot.
The top five cited new conditions include:
21% autoimmune
20% blood clots
19% stroke/lung clots
17% liver damage/leg clots/heart attack
15% disrupted menstrual cycle/Guillain-Barré/Bell’s palsy
Regarding describing the conditions, 47% report mild, 43% report serious and 10% report severe/still recovering.
Describing their experience with taking one or more COVID-19 vaccines, 58% report it was a good decision, 28% are neutral and 14% regret it.
Finally, 30% of those ages 18-49 report knowing someone else who has been medically diagnosed within a matter of weeks to several months after taking a COVID-19 vaccine.
The top five cited medically diagnosed conditions of the person known by those under age 50 are:
30% blood clots
23% stroke
20% autoimmune
18% leg clots/lung clots
17% heart attack
In other findings:
Regarding trust in the government to handle future pandemics among the all-adults survey — 23% say it has increased, 34% say it has decreased, 32% say it has remained the same, the rest were unsure.
The surveys included 1,038 American adults of all ages (MOE +/- 3.1) and 829 18-49-year-olds (MOE +/- 3.5) Both polls were fielded July 22-24, and data sets were pre-stratified and weighted to be representative of their respective populations. Error margins are higher for subgroups.
For questions, wording and full results, see ALL ADULTS and 18-49.
Fed Ct Says Walgreens is Immune from Liability Under the Prep Act: Woman Fell in the Parking Lot after Getting COVID Shot. All who Administer Shots are Immune Unless there was Willful Misconduct
/From [HERE] Walgreen Co. is immune from a customer’s suit seeking damages for injuries she suffered in a fall after receiving her Covid-19 vaccine, a federal court in New Mexico said.
The Public Readiness and Emergency Preparedness Act provides an exclusive, administrative remedy for “any claim for loss that has a causal relationship with the administration to or use by an individual of a covered countermeasure” such as a vaccine, the US District Court for the District of New Mexico said.
Suzanne Storment’s injuries directly related to Walgreens’ administration of the vaccine, and therefore weren’t actionable, the court said.
Storment received her first Covid-19 vaccination at a Walgreens store in Albuquerque in February 2021. There were no chairs to sit on while waiting to see if there were any untoward effects, so Storment went out to the parking lot to sit in her car.
Once in the parking lot, Storment felt dizzy and fell to the pavement, fracturing her elbow in multiple places. She sued Walgreens for damages.
Congress, in the PREP Act, “plainly provided immunity under both federal and state law with respect to all claims for loss” arising from the administration of the vaccine, the court said.
The PREP Act's cause of action permits suits only for “willful misconduct.” 42 U.S.C. § 247d-6d(d)(1). The Act defines “willful misconduct” as “an act or omission that is taken-(i) intentionally to achieve a wrongful purpose; (ii) knowingly without legal or factual justification; and (iii) in disregard of a known or obvious risk that is so great as to make it highly probable that the harm will outweigh the benefit.” Id. § 247d-6d(c)(1)(A). The Act further specifies that willful misconduct “shall be construed as establishing a standard for liability that is more stringent than a standard of negligence in any form or recklessness.” Id. § 247d-6d(c)(1)(B).
Storment’s injury “is unfortunate and certainly deserving of a remedy,” the court said. But it can’t be divorced from the administration of the vaccine. The PREP Act therefore applies and provides Walgreens with immunity, Judge Margaret I. Strickland said in Wednesday’s opinion.
Branch Law Firm represents Storment. Modrall Sperling represents Walgreens.
The case is Storment v. Walgreen Co., 2022 BL 261083, D.N.M., No. 1:21-cv-898, 7/27/22.
Dr Fleming says 'There is No Benefit to COVID Shots. Vax is a Bioweapon Making the Vaccinated Susceptible to Disease and Death. Companies Must Be Held Accountable, Gain of Function Research Stopped'
/From [HERE] Dr Richard Fleming is an American Medical Doctor, specialising in cardiology and has a law degree. He is a Fellow of the American College of Physicians and a Fellow of the American Society of Internal Medicine, he is a medical patent expert, has authored between 400 and 500 medical papers, and has sat on review boards of medical journals.
In March this year, he testified that:
SARS-CoV-2 is a lab-engineered bio-weapon, funded by the US government, the result of gain-of-function research on the spike protein, making it more infectious.
Safe and Effective treatments for the virus were suppressed by the US health regulatory agencies.
Quarantining of healthy people is completely ineffective.
The mRNA/RNA “vaccines” produced by Pfizer, Moderna and Janssen are bio-weapons delivering the same toxic spike protein as the virus but in loads up to 5 million times higher.
The vaccinated are responsible for pressure-selecting variants (alpha, delta, omicron, etc.), prolonging the epidemic.
The “vaccine” disrupts the natural immune system, making the vaccinated more susceptible to infection and disease.
The “vaccine” damages red-blood cells and causes hyper-inflammatory and clotting that cause disease and death in its own right.
Did MoneyPox Arise Naturally? Evidence Suggests US/China Authorities Created the Virus, Its Treatment and "The Emergency" [reality construction] for More Liability Free Profit and Control Over Sheeple
/STORY AT-A-GLANCE
By the third week of July 2022, some 16,000 cases of monkeypox had been recorded across 75 countries, with the vast majority of cases occurring among homosexual and bisexual men. In the U.S., recorded cases were around 3,000, including two children
July 23, 2022, World Health Organization Director-General Tedros Adhanom Ghebreyesus unilaterally overruled this panel of advisers and declared monkeypox a “public health emergency of international concern” (PHEIC). Ghebreyesus made the decision to declare a PHEIC even though the WHO’s advisory panel opposed the declaration 9 to 6
According to Ghebreyesus, “for the moment this is an outbreak that is concentrated among men who have sex with men, especially those with multiple sexual partners. That means that this is an outbreak that can be stopped with the right strategies in the right groups”
At present, the PHEIC appears to be financially motivated. Moderna is testing an mRNA injection for monkeypox, and in addition to the two smallpox vaccines already approved, Aventis Pasteur also has a smallpox vaccine that, while still investigational, could receive emergency use authorization
Disturbingly, in February 2022, the Wuhan Institute of Virology published a study in which they describe creating a portion of a monkeypox genome from scratch in order to develop a PCR test for monkeypox diagnosis. The National Institutes for Health in the U.S. also began studying a monkeypox drug in 2020
CDC Official Used Purposefully Flawed Data to Justify COVID Shots for Infants and Children Analysis Shows
/From [CHD] An official with the Centers for Disease Control and Prevention (CDC) used data from a flawed preprint study that exaggerated the risk of death for children from COVID-19 in her presentations to CDC and U.S. Food and Drug Administration (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.
Study falsely claimed COVID was leading cause of death in U.S. children
During a June 17 meeting of its Advisory Committee on Immunization Practices to discuss pediatric COVID-19 vaccines in children under 5, Dr. Katherine Fleming-Dutra, a pediatrician and pediatric emergency medicine physician with the CDC, presented a table that falsely claimed COVID-19 was a leading cause of death in U.S. children.
Fleming-Dutra earlier that week presented the same table during the FDA’s vaccine advisory committee meeting, along with other slides from the original U.K. study that also falsely claimedCOVID-19 as a “top 5 cause of death” in children.
The table, which was sourced from the U.K. study, was disseminated widely by physicians on Twitter who claimed the data “made the case” for vaccinating children under 5.
Emails Reveal Biden, Pharma Pressured Top FDA Officials to Approve Booster Timeline
/From [CHD] Judicial Watch today announced it received 112 pages from the U.S. Food and Drug Administration (FDA) that show top officials being pressured by “companies and for that matter the administration, who try to impose timeless [sic] that make no sense.”
The records were produced to Judicial Watch in response to a February Freedom of Information Act (FOIA) lawsuit against the Department of Health & Human Services (HHS) that was filed after HHS failed to respond to a Sept. 3, 2021, FOIA request for records of communication from the former director and deputy director of the FDA’s Office of Vaccines Research and Review, Dr. Marion Gruber and Dr. Philip Krause, respectively (Judicial Watch v. U.S. Department of Health and Human Services (No. 1:22-cv-00292)).
Drs. Gruber and Krause reportedly resigned during the White House’s push to approve the COVID-19 vaccine “booster shots.”
On Sept. 13, 2021, Gruber and Krause were among a group of resigning doctors who agreed that, “available evidence doesn’t yet indicate a need for COVID-19 vaccine booster shots among the general population …”
The records include an Aug. 25, 2021, email by Marion Gruber to her boss, Center for Biologics Evaluation and Research (CBER) Director Peter Marks:
“Over the last couple of days, Janssen has bombarded us with emails regarding their booster dose studies.
“I am also very concerned that companies (such as Pfizer and Janssen) are trying to put pressure on OVRR [Office of Vaccines Research and Review] by way of PR [public relations]. We need to be given time to consider their data and cannot be pushed by these companies and for that matter the Administration, who try to impose timeless [sic] that make no sense (e.g., Sep 20)…. It appears that at least Pfizer’s data will not be aligned with this approach and the ‘n’ [test numbers] they have is grossly insufficient. Obviously, we have to review the data but we have taken a peek and have serious concerns.
“Lastly, and this is my personal opinion, data we have seen so far from various companies (Pfizer, Janssen, Moderna) appear to suggest that boosters are not needed.”
In an email exchange on Aug. 27, 2021, Gruber replies to an email from Maureen Hess, a communications specialist at the Center for Biologics Evaluation and Research:
“Well, the message appears to be ‘total buy-in in the need for boosters,’ this is not how I am writing the BD [likely board decision], I am trying to take a more neutral approach. This piece sounds as if we already decided to approve this supplement.”
Hess responds, “Okay, I’ll make some additional edits (but JW [likely Acting FDA Commissioner Janet Woodcock] was included on this statement so our edits may be rejected above us.”
After sending more emails about edits Hess made, Gruber replies, “From my perspective, this is as good as it can get. Obviously, this statements [sic] puts us into a real bind but the damage is already done.”
In an Aug. 20, 2021, email exchange Dr. Doran Fink, the Deputy Director of the FDA’s Division of Vaccines and Related Products Applications raises questions regarding new data, that Moderna was submitting to FDA about its COVID vaccine. Fink told Drs. Gruber, Krause and other colleagues:
“I had to bite my tongue when Peter [likely Dr. Peter Marks, Director of the Center for Biologics Evaluation and Research] mentioned this morning we wouldn’t be doing rushed reviews anymore so as not to ask about the booster doses that the administration promised to everyone by Sept 20!
“And then there is the question of the data that will support these booster doses — maybe I’m wrong, but my understanding is that Pfizer is proposing that their sBLA include the Phase 1 booster data from a grand total of 23 subjects. I’m not sure what Moderna will have, but the data Fauci presented in the press conference from NIAID studies, which was ~25 subjects per treatment arm.”
Gruber states in an Aug. 17, 2021, email “They [Dr. Doran’s team] fully understand that the Acting Commissioner would like to approve this product [Pfizer COVID booster vaccine] very soon and are trying their best to complete their review and assessment, while at the same time, maintaining our high standards and scientific and clinical integrity.”
Philip Krause, in an Aug. 10, 2021 email, complains: “It sounds like Peter [likely Center for Biologics Evaluation and Research Director Peter Marks] thinks he has taken over all vaccine operations, not just the Pfizer BLA [Biologics License Application] …”
On Aug. 23, 2021, Dr. Arnold Monto, professor in the Department of Epidemiology of the University of Michigan School of Public Health, emails Drs. Gruber and Krause using the subject “VRBPAC and boosters.”
The email said:
“The Surgeon General last night made a statement that the FDA and CDC advisory committees would be reviewing Hope that he misspoke about the VRBPAC (Vaccines and Related Biological Products Advisory Committee) Doesn’t seem to be enough time to get it organized Just got asked about flu vaccination and COVID boosters being given at the same time. Gave my personal information, don’t”
Gruber then replies to Monto: “We will be discussing the ‘booster question’ and related submissions including whether VRBPAC should be held. We do not know yet and you are right that timing will be an issue once again.”
On Sept. 22, 2021, the FDA approved the use of a booster dose of the Pfizer drug.
According to the organization’s news release, the FDA, “amended the emergency use authorization (EUA) for the Pfizer-BioNTech COVID-19 Vaccine to allow for use of a single booster dose, to be administered at least six months after completion of the primary series” for people at “high risk” of “severe COVID-19.”
“These FDA documents confirm a politicized approval process for the controversial COVID-19 vaccine booster shots,” says Judicial Watch President Tom Fitton. “It is a scandal that it took months and a federal lawsuit to these troubling facts about this unprecedented and seemingly never-ending vaccine operation.”
Through FOIA requests and lawsuits, Judicial Watch has uncovered a substantial amount of information about COVID-19 issues:
Recently, National Institutes of Health (NIH) records revealed an FBI “inquiry” into the NIH’s controversial bat coronavirus grant tied to the Wuhan Institute of Virology. The records also show National Institute of Allergy and Infectious Diseases (NIAID) officials were concerned about “gain-of-function” research in China’s Wuhan Institute of Virology in 2016. The Fauci agency was also concerned about EcoHealth Alliance’s lack of compliance with reporting rules and use of gain-of-function research in the NIH-funded research involving bat coronaviruses in Wuhan, China.
HHS records revealed that from 2014 to 2019, $826,277 was given to the Wuhan Institute of Virology for bat coronavirus research by the NIAID.
NIAID records showed that it gave nine China-related grants to EcoHealth Alliance to research coronavirus emergence in bats and was the NIH’s top issuer of grants to the Wuhan lab itself. The records also included an email from the vice director of the Wuhan Lab asking an NIH official for help finding disinfectants for decontamination of airtight suits and indoor surfaces.
HHS records included an “urgent for Dr. Fauci” email chain, citing ties between the Wuhan lab and the taxpayer-funded EcoHealth Alliance. The government emails also reported that the foundation of U.S. billionaire Bill Gates worked closely with the Chinese government to pave the way for Chinese-produced medications to be sold outside China and help “raise China’s voice of governance by placing representatives from China on important international counsels as high-level commitment from China.”
HHS records included a grant application for research involving the coronavirus that appears to describe “gain-of-function” research involving RNA extractions from bats, experiments on viruses, attempts to develop a chimeric virus and efforts to genetically manipulate the full-length bat SARSr-CoV WIV1 strain molecular clone.
HHS records showed the State Department and NIAID knew immediately in January 2020 that China was withholding COVID data, which was hindering risk assessment and response by public health officials.
University of Texas Medical Branch (UTMB) records show the former director of the Galveston National Laboratory at the University of Texas Medical Branch (UTMB), Dr. James W. Le Duc warned Chinese researchers at the Wuhan Institute of Virology of potential investigations into the COVID issue by Congress.
HHS records regarding biodistribution studies and related data for the COVID-19 vaccines show a key component of the vaccines developed by Pfizer/BioNTech, lipid nanoparticles (LNPs), were found outside the injection site, mainly the liver, adrenal glands, spleen and ovaries of test animals, eight to 48 hours after injection.
Records from the Federal Select Agent Program (FSAP) reveal safety lapses and violations at U.S. biosafety laboratories that conduct research on dangerous agents and toxins.
HHS records include emails between NIH then-Director Francis Collins and Anthony Fauci, the director of the NIAID, about hydroxychloroquine and COVID-19.
HHS records show that NIH officials tailored confidentiality forms to China’s terms and that the World Health Organization (WHO) conducted an unreleased, “strictly confidential” COVID-19 epidemiological analysis in January 2020.
Fauci’s emails include his approval of a press release supportive of China’s response to the 2019 novel coronavirus.
Response to FOIA Request Reveals the US Government Colluded with Twitter, Google and Fakebook to Suppress Information Posted About the Dangers of COVID Shots and Intentionally Destroy Informed Consent
/From [HERE] A number of documents described as “the tip of the iceberg” have been made public, revealing communications between private tech giants and the US administration bodies, aimed at closely coordinating censorship of Covid topics on social media.
This was announced on Wednesday by America First Legal (AFL)nonprofit, which obtained the documents thanks to a lawsuit filed against the Centers for Disease Control and Prevention (CDC). The legal action came after a failed attempt to, through Freedom of Information Act (FOIA) requests, learn about the level of the involvement of the White House in this type of censorship.
The communications are interpreted as providing yet another piece of evidence of coordination, or even collusion, between US authorities and Google, Twitter, and Facebook.
AFL was spurred to action after Jen Psaki, at the time White House press secretary, last July declared that the administration was “regularly making sure” to inform social networks about what it identifies as narrative dangerous to public health. “And we work to engage with them to better understand the enforcement of social media platform policies,” Psaki said.
The emails that have now finally been released show that CDC maintained regular communication with the three biggest social platforms starting in December 2020 and for at least another six months. These exchanges reveal what “working” with Google and others looked like: it went as far as flagging posts by social sites’ users as “examples” of what needs to be censored.
Ad money was also a building block in this unusual and secretive form of close cooperation that could eventually bring into question the status of Big Tech corporations as private entities not bound by the First Amendment. In April of last year, Facebook gave CDC $15 million-worth of ad credits as a “gift” to be used to spread the agency’s messages on vaccines, social distancing, travel and other Covid restrictions.
In other emails, Twitter employees are arranging regular chats with CDC, while the agency at one point in the spring of last year warned Facebook that its algorithms are not doing a good job – because along with vaccine “misinformation” they also were also getting rid of some posts by public health institutions.
An interesting detail concerns a high-ranking CDC official appearing at Google’s Trusted Media Summit in 2020, but not allowing organizers to post their address on YouTube – because they were not authorized to speak publicly. [MORE]
Best Interest of the Child? Robert Kennedy's Organization Denounces the COVID Injection Mandate for Kids in DC: It Violates the Right to Refuse Emergency Use Vaccines and Refuse Medical Treatment
/COVID INJECTIONS DON'T IMMUNIZE OR STOP SPREAD. THEY'RE TREATMENTS (NOT VACCINES) THAT FEED THE VIRUS AND FACILITATE ITS DEVELOPMENT INTO MORE VARIANTS. YES THE GOVERNMENT IS TRYING TO KILL YOU AND YOUR CHILDREN.
From [CHD] Schools in Washington, D.C., will require all students ages 12 and older to get the COVID-19 vaccine before they can attend school in the fall, despite warnings from legal experts who say the mandate violates federal law.
The Office of the State Superintendent of Education announced on July 19 that student immunization requirements for the upcoming 2022-2023 school year will include the COVID-19vaccine for all students who are of an age for which there is a vaccine fully approved by the U.S. Food and Drug Administration (FDA).
“On July 8, 2022, the FDA fully approved the COVID-19 vaccine commonly known as the Pfizer-BioNTech COVID-19 Vaccine for individuals 12 to 15 years old,” said State Superintendent of Education Christina Grant in a press release.
“The approval of the Pfizer-BioNTech COVID-19 vaccine for individuals 12 to 15 means that, unless exempted, any student age 12-15 at the start of the 2022-23 school year must have received the primary COVID-19 vaccine series or have started receiving the shot by Sept. 16, 2022,” she said.
“We want to make sure that all of our students have everything they need for a healthy start to the school year,” Grant added. “This means making sure children see their primary medical provider for a well-child visit and receive all needed immunizations.”
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.
CHD demands D.C. Schools rescind mandate
In a letter sent today to Grant, Robert F. Kennedy, Jr., chairman and chief legal counsel for Children’s Health Defense (CHD), asked Grant to rescind the program or CHD would sue to overturn the mandate.
Kennedy said Grant’s press release was incorrect because the Pfizer-BioNTech COVID-19 vaccine was never fully approved and still remains under Emergency Use Authorization (EUA).
The FDA earlier this month granted full approval to Pfizer’s Comirnaty COVID-19 vaccine for adolescents 12 through 15 years old, without convening its vaccine advisory panel.
In August 2021, the agency granted full licensing of the Comirnaty vaccine for ages 16 and older.
However, there are no Comirnaty-labeled vaccines available in the U.S., for any age group.
Although courts have upheld many childhood vaccination requirements for licensed and approved vaccines, no court has ever upheld a mandate for schoolchildren for an EUA vaccine, according to Kennedy.
Kennedy wrote:
“In fact, a District of Columbia United States District Court held that EUA vaccines cannot be mandated to soldiers in the U.S. military, who enjoy far fewer rights than civilians. Doe #1 v. Rumsfeld, 297 F.Supp.2d 119 (2003). That court held: ‘… the United States cannot demand that members of the armed forces also serve as guinea pigs for experimental drugs.’ Id. at 135.
“Federal law 21 U.S.C. § 360bbb-3(e)(1)(A)(ii)(III) requires that the person to whom an EUA vaccine is administered be advised, ‘of the option to accept or refuse administration of the product, of the consequences, if any, of refusing administration of the product, and of the alternatives to the product that are available and of their benefits and risks.’
“The reason for the right of refusal stems from the fact that EUA products are by definition experimental.
“Under the Nuremberg Code, a universal legal norm, no one may be coerced to participate in a medical experiment. Consent of the individual is ‘absolutely essential.’ The liability for forced participation in a medical experiment, not to mention liability for injury from such coerced medical intervention, may be incalculable.”
Commenting on the D.C. mandate, CHD President Mary Holland said, “It violates fundamental human rights and international law to force people, and especially children, to take experimentalmedical products.”
“We sincerely hope the District will reconsider its misguided policy for schoolchildren,” Holland added.
Another organization — Liberty Counsel — said it may also challenge the District of Columbia’s vaccine mandate.
“There is no FDA-approved COVID shot available and therefore, individuals have a right under the emergency use authorization to refuse these shots,” Matthew Staver, founder and chairman of Liberty Counsel, told The Epoch Times.
Under the Federal Food, Drug, and Cosmetic Act, people receiving an EUA product must be advised that some benefits and risks “are unknown” and given the “option to accept or refuse administration of the product.”
“It is your choice to receive or not receive [the vaccine],” Staver said. “Should you decide not to receive it, it will not change your standard medical care,” according to FDA fact sheets on EUA COVID-19 vaccines.
Several other school systems have attempted, so far unsuccessfully, to implement a COVID-19 vaccine mandate:
• Louisiana: The Louisiana Department of Health in May said it would no longer seek to make COVID-19 vaccines mandatory for the upcoming school year because the shot had not receivedfull FDA approval for people under the age of 16.
The decision came after CHD and thousands of concerned parents on March 16 filed an amicus brief in a lawsuit seeking to stop the Louisana Department of Health from adding COVID-19 vaccines to the state’s school immunization schedule.
The joint lawsuit was filed in December 2021, by Louisiana Attorney General Jeff Landry and state Rep. Raymond Crews against Gov. John Bel Edwards after he announced COVID-19 vaccines would be mandatory for all children age 5 and over at public or private schools.
• Los Angeles: Los Angeles Unified School District (LAUSD) Superintendent Alberto Carvalho on April 28 recommended the district postpone its COVID-19 student vaccination mandate until at least July 2023 because the FDA had not fully approved the COVID-19 vaccine for all ages covering grades 7 through 12.
LAUSD officials announced last fall students 12 and older would be required to be vaccinated by the start of the 2022-2023 school year but delayed the mandate because tens of thousands of students still had not complied with the requirement.
• Washington: The Washington State Board of Health in April voted unanimously against adding COVID-19 vaccines to the requirements for students to attend K-12 schools this fall after its advisory group recommended against the requirement. The board said more data was needed about vaccines for ages 5 to 11 and raised concerns that the Pfizer-BioNTech vaccine has yet to be fully approved for ages 5 to 15.
If the Numbers are Correct the Majority of the World’s Population Has Been Poisoned by COVID Injections. Blight Supremacy Depopulation Agenda Working as Deaths Pile Up
/According to "FUNKTIONARY, THE KEY HOLDERS ENPSYCHLOPEDIA"
genocide – the intentional decreasing of the people of a given population or asili, particularly in the interests of another population or value-system that wishes to control the resources of the victims. 2) the-cide-show of the World Health Organization (WHO). Blindness to economic reality has placed mankind in a very precarious position. Our freedom and very lives depend on how (and how soon) we resolve resource misapplication and inequalities. (See: Population Control)
UK Government Data Demonstrates COVID Shots are Most Likely the Cause of ‘Sudden Adult Death Syndrome’
/From [EXPOSE] Doctors are allegedly baffled at what is causing a sudden uptick in what they have dubbed ‘Sudden Adult Death Syndrome’ among adults under the age of 40 over the past year, and are now urging all under 40’s to go and get their heart checked.
But these doctors need not remain “baffled” any longer because we have rock-solid evidence that the Covid-19 vaccine is to blame.
Official UK Office for National Statistics data shows vaccinated adults aged 18 to 39 have a 92% higher mortality rate (per 100,000) than unvaccinated adults.
Official Public Health Scotland data reveals there has been a 67% increase compared to the historical average in the number of 15 to 44-year-olds suffering heart attacks, cardiac arrest, myocarditis, stroke, and other cardiovascular diseases since this age group was first offered the Covid-19 injection.
And figures published by NHS England in response to a freedom of information request show that ambulance call-outs for heart illness have doubled among all age groups including the under 30’s since the beginning of the Covid-19 vaccination campaign.
Healthy young people are dying suddenly and unexpectedly from what doctors are dubbing “a mysterious syndrome” and these same doctors are now seeking answers through a new national register.
People aged under 40 are now being urged to have their hearts checked because doctors claim they may potentially be at risk of Sudden Adult Death Syndrome.
Doctors say the syndrome, known as SADS, has been fatal for all kinds of people regardless of whether they maintain a fit and healthy lifestyle.
“SADS is an umbrella term to describe unexpected deaths in young people”, said The Royal Australian College of General Practitioners.
But it turns out the term is actually used when a post-mortem cannot find an obvious cause of death, and the reason doctors are struggling to find an obvious cause of death is that we’re now seeing thousands of deaths due to something that was impossible to occur prior to 2021. Covid-19 vaccination.
This becomes obvious once you know where to look. But the problem is doctors are actively discouraged from looking and it is not publicised in the mainstream media. However, all the answers doctors are looking for to explain what they are dubbing Sudden Adult Death Syndrome, are contained in official Government data.
Vaccinated Young Adults have a 92% higher mortality rate (per 100,000) than Unvaccinated Young Adults
The Office for National Statistics (ONS) is the UK’s largest independent producer of official statistics and the recognised national statistical institute of the UK. It is responsible for collecting and publishing statistics related to the economy, population and society at national, regional and local levels.
An ONS dataset on deaths in England by vaccination status can be found here. It contains a large amount of data on age-standardised mortality rates for deaths by vaccination status between 1 January 2021 and 31 January 2022.
Table 2 of the dataset contains data on the monthly age-standardised mortality rates by vaccination status by age group for all deaths in England. The following table shows an example of how the numbers are presented in the dataset –
What immediately catches the eye when looking at this data is the mortality rate per 100,00 person-years among 18-39-year-olds in the month of January 2021. The figures show the death rate among the unvaccinated in this month was 67.7 deaths per 100,000 person-years. Whilst the death rate among the partly vaccinated (at least 21 days ago) was 119.9 deaths per 100,000 years.
This shows that vaccinated 18-39-year-olds were more likely to die in January 2021, suggesting the Covid-19 injections increased the risk of death or played a part in causing death. So we dug further and extracted all the figures on 18-39-year-olds for each month between January 2021 and January 2022, and this is what we found –
The above chart shows the monthly age-standardised mortality rates by vaccination status for all-cause deaths, per 100,000 person-years among adults aged 18 to 39 in England. The green line is the mortality rate among the unvaccinated, which while fluctuating has remained pretty stable throughout.
The other lines however represent different vaccination statuses, and they are extremely concerning. The orange, yellow, and pink lines represent mortality rates within 21 days of receiving a first, second or third dose. And they reveal that the risk of death increases significantly immediately after vaccination.
But the most concerning figures are the mortality rates among those vaccinated at least 21 days ago, which you can see more clearly in the following chart –
What’s most concerning here is that the second injection seems to make things much worse in terms of the risk of death.
The highest mortality rate among the double vaccinated (at least 21 days ago) occurred in September 2021, with 125.9 deaths per 100,000 person-years. In the same month, the mortality rate among the unvaccinated equated to 46.8. Meaning the double vaccinated mortality rate was 169% higher than the unvaccinated mortality rate.
But the largest statistical difference occurred in November 2021. The mortality rate among the unvaccinated equated to 33.4 deaths per 100,000 person-years, whereas the mortality rate among the double vaccinated equated to 107. A difference of 220.4%.
The following chart shows the average-age standardised mortality rate to have occurred between 1st Jan 21 and 31st Jan 22 by vaccination status for all-cause deaths, per 100,000 person-years among adults aged 18 to 39 in England – [MORE]
Profiteers at Pfizer Reach Cosmic High of $27 Billion in Record Sales in 2021 Off its Deadly COVID Shots that Have Government Granted Immunity for Any Injury or Death it Causes
/From [HERE] Thanks to its COVID shots and its COVID infection antiviral treatment, Paxlovid, Pfizer has marked a record high in its quarterly sales. In all, the company’s revenue increased by 47%, top $27.7 billion in 2021.
It’s expecting even more in 2022, with an anticipated $32 billion incoming from its COVID jab and $22 billion for Paxlovid. Complete immunity fuels the cosmic profits.
The federal government has given complete immunity to Pfizer, Moderna, and J&J for any injury caused by their Covid-19 vaccines. That’s right: you cannot sue them if you are injured by their Covid-19 vaccine. (See Note 1 to read the law yourself.) So, while their product may not give you immunity, Pfizer and Moderna are guaranteed immunity. Said immunity also shields doctors, hospitals and any other persons who administer or coerce people to take deadly COVID injections.
And it gets even worse. These companies are even immune for – hold your breath – willful misconduct. That may sound crazy, but it is shockingly true. You can only sue them for willful misconduct if the federal government first sues them for such conduct. (See Note 2 below to read the law yourself.) And what are the odds the federal government will do so after wildly promoting the vaccine? About as likely as the FDA ever admitting they promoted a vaccine that caused widespread harm. [MORE] and [MORE]
Note 1. Pursuant to 42 U.S.C. § 247d-6d the federal government “Declaration pursuant to section 319F-3 of the Public Health Service Act to provide liability immunity for activities related to medical countermeasures against COVID-19” provides that “manufacturers” of “any vaccine, used to treat, … prevent or mitigate COVID-19” shall enjoy “[l]iablity immunity ,” including, “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 [COVID-19 vaccine].”
Note 2. Pursuant to 42 U.S.C. § 247d-6d(c)(5) “If an act or omission by a manufacturer or distributor with respect to a covered countermeasure, which act or omission is alleged under subsection (e)(3)(A) to constitute willful misconduct, … such act or omission shall not constitute ‘willful misconduct’ … if—(i)neither the Secretary nor the Attorney General has initiated an enforcement action with respect to such act or omission; or (ii)such an enforcement action has been initiated and the action has been terminated or finally resolved without a covered remedy.”
Latest CDC Data Shows 29,970 People are Dead from Taking COVID Injections. Including a Healthy 9 Yr Old who Died 2 Weeks After the Shot. She had sore throat and stomach and chest pain prior to Death
/From [CHD] 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:
2,429 adverse events, including 81 cases rated as serious and 3 reported deaths.
4 reports of myocarditis and pericarditis (heart inflammation).
The CDC uses a narrowed case definition of “myocarditis,” which excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department.15 reports of blood clotting disorders.
23 reports of seizures.
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) (see image above) 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:
32,835 adverse events, including 1,849 rated as serious and 44 reported deaths.
62 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 97% of cases attributed to Pfizer’s vaccine.
657 reports of myocarditis and pericarditis with 645 cases attributed to Pfizer’s vaccine.
165 reports of blood clotting disorders with all cases attributed to Pfizer.
20 cases of postural orthostatic tachycardia syndrome (POTS) with all cases attributed to Pfizer’s vaccine.
U.S. VAERS data from Dec. 14, 2020, to July 22, 2022, for all age groups combined, show:
20% of deaths were related to cardiac disorders.
54% of those who died were male, 41% were female and the remaining death reports did not include the gender of the deceased.
The average age of death was 73.
As of July 22, 5,670 pregnant women reported adverse events related to COVID-19 vaccines, including 1,772 reports of miscarriage or premature birth.
Of the 3,623 cases of Bell’s Palsy reported, 51% were attributed to Pfizer vaccinations, 40% to Moderna and 8% to J&J.
900 reports of Guillain-Barré syndrome, with 42% of cases attributed to Pfizer, 30% to Moderna and 27% to J&J.
2,293 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
1,743 reports of myocardial infarction.
14,254 reports of blood-clotting disorders in the U.S. Of those, 6,378 reports were attributed to Pfizer, 5,112 reports to Moderna and 2,718 reports to J&J.
4,273 cases of myocarditis and pericarditis with 2,619 cases attributed to Pfizer, 1,450 cases to Moderna and 188 cases to J&J.
14 cases of Creutzfeldt-Jakob disease with 8 cases attributed to Pfizer, 5 cases to Moderna and 1 case to J&J.
270 cases of POTS with 165 cases attributed to Pfizer, 87 cases to Moderna and 17 cases to J&J.
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.
LA Mask Mandate is Called Off. But an Unelected Health Ruler Can Unilaterally Declare Emergency and Force Compliance w/Trivial Demands Whenever She Wants in Free Range Prison Disguised as a Democracy
/According to the LA Times, Citing declining cases, Los Angeles County Public Health Director Barbara Ferrer announced Thursday her department would not impose a mask mandate to deal with a summer surge fueled by super-contagious Omicron subvariants such as BA.5. [sheople are relieved. thanks master.]
But that does not mean L.A. County is out of the woods. [MORE]
She did not explain what she meant by “declining cases” as PCR tests do not and cannot measure COVID infection. Nor did she explain how masks are relevant to the “declining cases.”
According to FUNKTIONARY:
"authority" - (so-called)—a cartoon, an alleged image of the Law. 2) a cartoon clothed in flesh and blood. 3) the notion of an implied right and application of that "right" of individuals or groups of same to control or exercise external power over others, which has no meaning in reality. 4) power over...which is thoroughly institutionalized. 5) ruling through coercion. So-called "authority" is the justification for remaining impotent. The real threat to "authority" is the masses overcoming info-gaps and verigaps through self-knowledge and the proliferation of symbols of opposition, not crime or destruction of property.
"Authority-" is not a force but a farce! "Every great advancement in natural knowledge has involved the absolute rejection of authority." —Aldous Huxley. Government is the hefty price we pay for our lack of being further evolved as humans. "The disappearance of a sense of responsibility is the most far-reaching consequence of submission to authority." —Stanley Milgram Regarding obedience to authority and carrying out "orders" Milgram states, "Thus there is a fragmentation of the totai human act; no one man decides to carry out the evil act and is confronted with consequences. The person who assumes full responsibility for the act has evaporated. Perhaps this is the most common characteristic of socially organized evil in modern society." At its root, government is based on violence and coercion. [MORE]
Pfizer mRNA Injection Goes Into Liver and Changes into DNA according to Swedish Study
/From [HERE] The research was conducted at Lund University.
A new Swedish study published in MDPI found that the Pfizer vaccine goes into liver cells and converts to DNA, challenging claims so far that the mRNA COVID-19 vaccines do not change or interact with your DNA in any way.
It's the first time that researchers have shown in vitro - or inside a petri dish - how an mRNA vaccine is converted into DNA on a human liver cell line, the Epoch Times reported.
It's precisely what health experts and fact-checkers said for more than a year could not occur.
Dr. Peter McCullough, an internist, cardiologist and epidemiologist who is one of the leading critics of the COVID vaccines, said the findings have "enormous implications of permanent chromosomal change" that could drive a "whole new genre of chronic disease."
The CDC assures Americans that the mRNA and the spike protein it produces in COVID-19 vaccines to create an immune response "don't last long in the body." On its website, the agency states:
"Our cells break down mRNA and get rid of it within a few days after vaccination. Scientists estimate that the spike protein, like other proteins our bodies create, may stay in the body up to a few weeks."
Further, the CDC says on a web page titled "Myths and Facts about COVID-19 Vaccines" that the "genetic material delivered by mRNA vaccines never enters the nucleus of your cells."
However, the researchers at Lund University in Malmö, Sweden, found that the mRNA vaccine enters human liver cells and triggers the cell's DNA in the nucleus to increase the production of the LINE-1 gene expression to make mRNA.
The whole process occurred rapidly, within six hours, concluded the study, which was published by the university's Department of Clinical Sciences.
Pfizer did not comment on the study's findings, the Epoch Times reported, stating only that its mRNA vaccine does not alter the human genome.

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