Not Genocide but Genthanasia [a slow motion extermination]: Since Vax Rollout Death Claims Have Tripled. Media Conceals Reality that Record Numbers of People are Dropping Dead or Becoming Disabled

genthanasia - the non-violent weeding out of undesirables or the slow motion extermination of LARGE POPULATIONS OVER A PERIOD OF TIME THROUGH THE USE OF BIOWEAPONS, BIOCIDE, FAKE VACCINES, WATER AND FOOD POISONINGS, ETC. Benign extermination CARRIED OUT BY THE PATHOCRACY THROUGH SINGLE SOURCE MEDIA PROPAGANDA, CORPORATIONS AND GOVERNMENT AUTHORITIES. Subtler non-violent ethnic cleansing. [MORE]

From [HERE] This is the Afterword to Edward Dowd’s new book, “‘Cause Unknown’: The Epidemic of Sudden Deaths in 2021 and 2022.”

A quick thought experiment:

Imagine that thousands of healthy young Americans died suddenly, unexpectedly, mysteriously — and then kept dying at an alarming and escalating rate. (Once upon a time), that would trigger an urgent Centers for Disease Control and Prevention (CDC) inquiry to determine the cause of the deaths.

Imagine attentive and curious public health officials discover the decedents had all repeatedly ingested a new and little-understood drug. Next, the officials determine to a certainty that the drug these kids took has a clear mechanism of action for causing inflammation of the heart and other cardiac injuries in some people.

They learn that public health officials in other countries have seen the same thing and stopped recommending this same drug to young people. Next, some of the most senior and revered scientific advisors to the U.S. government publicly recommend the drug be stopped for young people.

Finally, thousands of doctors around the world sign petitions and write op-eds opposing the drug for young people. Experts from Harvard, Yale, MIT, Stanford and Oxford universities come forward to voice their concerns.

Alas, that thought experiment doesn’t require any imagination, because it’s exactly what’s occurred — except for the part about attentive and curious CDC officials rushing in to inquire. That part I had to make up.

In the pre-COVID-19 world, wouldn’t inquisitive reporters chase such a story, and wouldn’t the U.S. Food and Drug Administration (FDA) pause administration of the new mystery drug until a comprehensive inquiry was complete?

And above all, wouldn’t such a drug have quickly become a leading suspect worth considering for its possible role in the deaths?

BUY NOW: Ed Dowd’s Must-Read Book — “Cause Unknown”

Somehow, those have become rhetorical questions.

But not to Edward Dowd. His pioneering exploration of these sad sudden deaths was months ahead of the Wall Street Journal (WSJ) story about a lethal conundrum facing insurance companies.

Apparently, as mass vaccination progressed in 2021, excess death claims in working-age Americans tripled. Given the temporal relationship, might there be a connection between vaccines and these deaths?

Apparently not, because the WSJ story didn’t even mention mass vaccination among the causes worth considering:

  1. Delayed medical treatment from 2020

  2. People’s fear of seeking treatment

  3. Trouble lining up appointments

  4. Drug abuse and other societal troubles

  5. People not taking care of themselves

  6. Long COVID

  7. Not-yet-known long-term effects of COVID-19

  8. People dying later “from the toll COVID has taken on their bodies”

Numbers 1, 2 and 3 are all subsets of the same concept: impact of lockdowns and fear. Numbers 6, 7 and 8 are all subsets of the same concept: the impact of COVID-19 illness.

Aside from drug abuse and trouble getting doctors’ appointments, did anything else happen in 2021 that might possibly-maybe-perhaps-call-me-crazy be worth considering?

The insurers attributed most of the 2021 excess deaths to heart and circulatory issues, neurological disorders and stroke. It’s a coincidence, apparently, that nearly all of their deceased customers had just been injected with something known to cause heart and circulatory issues, neurological disorders and stroke.

Head-scratching by insurance industry CEOs and experts interviewed for the WSJ article was understandable, because, you know, how in the world could deaths possibly be linked to some brand new, never-before-used drug that was minimally tested, maximally rushed, mass-administered, and oh yeah, and by the way, is known to cause the very medical issues their customers were dying of?

(If you have any doubt as to whether the mRNA vaccines cause cardiac problems, see Appendix Four, Page 190, for a sampling of 100 published papers on vaccine-induced cardiac injuries to young people.) [MORE]

COVID Fraud and Battery: Suit Says a Racist Suspect Georgetown Doctor Forced 2 Black Kids to Get Vaxxed w/o Mom's Consent, Prevented Kids from Leaving Clinic and Consulting w/Mom who Was Outside Door

From [HERE] The mother of two children who were given COVID-19 vaccines without the mother’s consent is suing the doctor who administered the vaccines.

An attorney representing NaTonya McNeil last week filed a lawsuit in Superior Court for the District of Columbia against Janine A. Rethy, M.D., M.P.H.

According to the complaint, on Sept. 2, 2022, McNeil took her two older children, ages 15 and 17, to the KIDS Mobile Medical Clinic/Ronald McDonald Care Mobile clinic, operated by Georgetown Hospital, to complete their required annual physical exam for the 2022-2023 school year.

The lawsuit alleges Rethy, director of the mobile clinic, held the children in the examination room longer than necessary for a regular check-up and vaccinated them against COVID-19 over their objections and without consulting their mother

In order to attempt to obtain the children’s consent — which they are not legally able to provide without a parent or guardian — the doctor falsely informed the children the COVID-19 vaccine was mandatory for school attendance and told them they could not lawfully decline it if they wanted to attend school.

The suit, filed by D.C. attorney Matthew Hardin, seeks damages for false imprisonment, battery and fraud.

Children’s Health Defense (CHD) is financing the lawsuit because, according to CHD President and General Counsel Mary Holland, “CHD couldn’t just sit still and not allow this wrong to go unpunished and not bring this to the public’s attention.”

In an exclusive conversation with The Defender, McNeil explained why she is suing the the doctor:

“I just feel like people shouldn’t be able to do whatever they want to do to other people and especially not to children. As a mother, I feel like, ‘You all just took all my rights away from me to do what you wanted to do to my kids.’

“I do want justice to be done in this case. I feel like something needs to be done. This can’t just continue to happen.”

‘I feel violated’

According to the complaint, Rethy’s stated goal is to vaccinate all children against COVID-19. The complaint quotes her statement to the press:

“Our goal is to increase vaccination rates in children here in D.C. … For more than 30 years our role has been to be in the community to help address the problem of health disparities, bringing families care where they are.

“For this particular effort, we are glad to be partnering with DC Health to provide both regular childhood vaccines and COVID-19 vaccines to all children.”

In addition to her role as director of the mobile clinic, Rethy is chief of MedStar Georgetown University Hospital’s Division of Community Pediatrics and assistant professor of pediatrics at Georgetown University School of Medicine.

McNeil said that when she took her older children to the clinic, she stayed outside the examination room to care for her infant. As soon as the children entered the doctor’s office, she called her daughter’s cellphone to let Rethy know she was just outside the door if the doctor needed to consult her for anything.

According to McNeil, the doctor did not ask or inform her about any vaccinations, and did not ask her to sign anything. At the end of the physical, Rethy came out to talk to her.

McNeil said the doctor explained her son’s asthma treatment plan, but that’s all they discussed.

As they were heading home, McNeil said she was shocked when her daughter complained that her arm hurt “pretty bad.” When McNeil asked her why it hurt, her daughter said she was given the COVID-19 shot, even though she told the doctor she didn’t want it.

When McNeil asked her why she allowed the doctor to administer the shot, her daughter said:

“When she had the needle in her hand and she was coming towards me, I backed up and I asked her what is that needle, and she said it was the COVID shot and I … told her I didn’t want it and she said, ‘Well it is mandatory, you have to get it in order to go to school.’”

Rethy allegedly administered the shot to her daughter, and then to her son. McNeil said:

“He’s 14 and he said they didn’t even ask him if he wanted it or not, but when they gave it to him, he said he thought he had to get it because his sister got it.”

According to the complaint, both children received the  Pfizer/BioNTech vaccine, authorized for emergency use, and the meningococcal vaccine. Her son was also injected with TDaP.

Both children were upset and angry they had been coerced into vaccination, the complaint says.

No school mandate, despite what clinic and doctor alleged

When she got home, McNeil said she called the doctor’s office, and asked them why they vaccinated her children without her consent.

“I would have never consented to you all vaccinating my children,” she said. “I’m not vaccinated and I’m not getting vaccinated and my kids were never supposed to be vaccinated for COVID period, under no circumstances.”

She said the person on the phone said they were supposed to get them for school.

After hanging up, McNeil said she was “so irritated I even started crying” because she couldn’t believe “they put this poison” into her children’s bodies.

In July 2022, D.C. public schools imposed a vaccine mandate for schoolchildren ages 12 and up for the 2022-2023 school year. But on Aug. 26, just weeks after imposing the mandate, officials walked it back, postponing it until 2023.

That means when McNeil’s children saw the doctor, there was no school vaccine mandate in place, despite what the Rethy allegedly told the children.

The age of consent

The District of Columbia in March 2021 enacted the D.C. Minor Consent for Vaccination Amendment Act of 2020 (D.C. Minor Consent Act), allowing children 11 and older to consent to the administration of any vaccine — including COVID-19 shots — recommended by the Advisory Committee on Immunization Practices (ACIP) — without parental knowledge or consent if the medical provider believed “the minor is capable of meeting the informed consent standard.”

The law also required healthcare personnel to provide accurate immunization records to the Department of Health and to the student’s school, but not to parents with religious exemptions.

CHD and Parental Rights Foundation filed a lawsuit seeking a court order to declare the D.C. Act unconstitutional.

A judge for the U.S. District Court for the District of Columbia on March 18, 2022, granted a preliminary injunction prohibiting the D.C. mayor, Department of Health and public schools from enforcing the law.

That means at the time McNeil’s children visited the clinic, they could not legally provide consent to be vaccinated without their mother’s consent.

McNeil said:

“To do that to my little children, my innocent children. They took her rights. When she backed away from you [the doctor] and said she didn’t want it, that should have been the end of it.

“Or you [the doctor] should have called me on the phone to find out what I feel about the situation. But you [the doctor] basically told my child a lie so you [she] could do what you [she] wanted to do to my kid.”

Lawsuit Claims “Remdesivir,” the primary treatment for COVID in hospitals, Has Killed at Least 100,000 People and the USDA Knows It and Still Approves It and Provides Incentives for Its Usage

From [HERE] and [HERE] The antiviral drug remdesivir, brand name Veklury, is approved for use against COVID-19 despite research showing it lacks effectiveness and can cause high rates of organ failure

  • John Beaudoin is calling for a criminal investigation into remdesivir, citing data that it may have killed 100,000 people in the U.S.

  • Beaudoin received all the death certificates in Massachusetts from 2015 to 2022, finding 1,840 excess deaths from acute renal failure from January 1, 2021, to November 30, 2022, which he believes may be due to remdesivir

  • A study published in The Lancet found “no clinical benefit” from the use of remdesivir in hospitalized patients

  • The U.S. government pays hospitals a 20% upcharge on the entire hospital bill when remdesivir is used

The U.S. Food and Drug Administration authorized the experimental antiviral drug remdesivir, brand name Veklury, for emergency use against COVID-19 in May 2020.1 By October 2020, it had received full approval.2 It remains a primary treatment for COVID-19 in hospitals, despite research showing it lacks effectiveness3 and can cause high rates of organ failure.4

On Twitter, John Beaudoin is calling for a criminal investigation into the drug, citing data that it may have killed 100,000 people in the U.S. "They know," he says, "or they willfully refuse to know. Either way, it's homicide."5

Using drugs that cause organ failure, like remdesivir, isn't in the best interest of public health. The fact that U.S. health authorities have focused on this and similarly harmful drugs to the exclusion of all others, including older drugs with high rates of effectiveness and superior safety profiles, sends a very disturbing message.

Did Remdesivir Kill Thousands in Massachusetts?

Beaudoin has filed a lawsuit in U.S. District Court and believes a spike in deaths from acute renal failure (ARF) in Massachusetts is due to remdesivir, which is produced by Gilead Sciences. Using a Freedom of Information Act (FOIA) request, Beaudoin received all the death certificates in Massachusetts from 2015 to 2022.

He then graphed the FOIA data, finding 1,840 excess deaths from acute renal failure from January 1, 2021 to November 30, 2022. Beaudoin also revealed an increase in deaths from acute rental failure in every age group over 15 years old, from 2015 to 2022.6 "Thousands dead in Massachusetts ARF likely due to Remdesivir. This requires CRIMINAL investigation," he tweeted.7

Deaths, Kidney Injury Common With Remdesivir

Remdesivir use didn't become widespread until 2020. From that time until October 2021, at least 7,491 adverse drug reactions were reported to the World Health Organization's (WHO) VigiAccess, including 560 deaths, 550 serious cardiac disorders and 475 acute kidney injuries.8

For comparison, only 5,674 adverse drug reactions were reported for ivermectin from 1992 to October 13, 2021.9 Despite its strong safety profile and efficacy, ivermectin was widely vilified during the pandemic. Not to mention, remdesivir costs between $2,340 and $3,120,10 while the average treatment cost for ivermectin is $58.11 Do you think this has anything to do with remdesivir's promotion and ivermectin's vilification?

While WHO updated its guidance in April 2022 to recommend the use of remdesivir in "mild or moderate COVID-19 patients who are at high risk of hospitalization,"12 a study published in The Lancet found "no clinical benefit" from the use of remdesivir in hospitalized patients.13 Further, the investigators believed three deaths during the study were related to remdesivir.14

Gilead's Political Ties Questioned as Remdesivir Use Persists

Still, the question remains why remdesivir continues to be used at all. In November 2020, WHO issued a bulletin recommending against the use of remdesivir in COVID-19 patients, stating, "There is currently no evidence that remdesivir improves survival and other outcomes in these patients."15

Is it possible that Gilead's strong political connections have influenced the government's approvals and recommendations? It's worth noting that Donald Rumsfeld was the chairman of Gilead from 1997 until he joined the Bush administration in 2001. Rumsfeld had previously served as secretary of defense under President Gerald Ford from 1975 to 1977, and again under President George W. Bush from 2001 to 2006.

FDA Even Approved Remdesivir for Children

In late April 2022, the FDA even approved remdesivir as the first and only COVID-19 treatment for children under 12, including babies as young as 28 days,16 an approval that boggles the mind, considering COVID-19 is rarely serious in children while remdesivir is ineffective and carries a risk of serious, and deadly, side effects.

What's worse, the drug is also approved for outpatient use in children, which is a first. Dr. Meryl Nass expressed her concerns about the FDA's approval of remdesivir for outpatient use in babies, stating:17

"The FDA just licensed Remdesivir for children as young as one month old. Both hospitalized children and outpatients may receive it. The drug might work in outpatients, but the vast majority of children have a very low risk of dying from COVID. If 7 deaths per 1,000 result from the drug, as … European investigators thought18 … it is possible it will harm or kill more children than it saves.

Shouldn't the FDA have waited longer to see what early outpatient treatment did for older ages? Or studied a much larger group of children? Very little has been published on children and remdesivir …

When we look at the press release issued by Gilead,19 we learn the approval was based on an open label, single arm trial in 53 children, 3 of whom died (6% of these children died); 72% had an adverse event, and 21% had a serious adverse event."

More Lawsuits Filed Against Remdesivir

Two women are suing Kaiser Permanente and Redlands Community Hospital in California for giving remdesivir to their husbands without consent. Both men died from kidney and organ failure after being administered remdesivir. "The day he was admitted on August 12 they started the remdesivir and on [August 17] is when they were done," Christina Briones told CBS News. "Five doses. [On] the 17th his kidneys started to fail."20

In California, lawsuits have been filed on behalf of at least 14 families against medical providers for prescribing remdesivir without providing necessary information about it, leading to the patients' deaths.21 Another wrongful death suit was filed in Nevada, after a patient died of kidney failure and respiratory failure a week after being given remdesivir.22

Safety Signal Revealed for Remdesivir and Kidney Failure

Meanwhile, a study published in Clinical Pharmacology and Therapeutics in April 2021 detected a potential safety signal for remdesivir and acute renal failure:23

"The combination of the terms 'acute renal failure' and 'remdesivir' yielded a statistically significant disproportionality signal with 138 observed cases instead of the nine expected. ROR [reporting odds ratio] of ARF with remdesivir was 20-fold that of comparative drugs.

Based on ARF cases reported in VigiBase, and despite the caveats inherent to COVID-19 circumstances, we detected a statistically significant pharmacovigilance signal of nephrotoxicity associated with remdesivir, deserving a thorough qualitative assessment of all available data."

In May 2021, another pharmacovigilance analysis revealed red flags against remdesivir. "Compared with the use of chloroquine, hydroxychloroquine, dexamethasone, sarilumab, or tocilizumab, the use of remdesivir was associated with an increased reporting of kidney disorders," the study found.24 It concluded:25

"Our findings, based on postmarketing real-life data from >5000 COVID-19 patients, support that kidney disorders, almost exclusively AKI [acute kidney injury], represent a serious, early, and potentially fatal adverse drug reaction of remdesivir. These results are consistent with findings from another group. Physicians should be aware of this potential risk and perform close kidney monitoring when prescribing remdesivir."

In March 2022, yet another pharmacovigilance analysis warned of a significant association between remdesivir and acute kidney injury, especially in male patients and those over the age of 65 years. "Although causality was not confirmed," they noted, "the association between remdesivir and AKI should not be ignored, especially in the older, male COVID-19 inpatients."26

US Government Pays Hospitals to Use Remdesivir

Remdesivir was developed as an antiviral drug and tested during the Ebola breakout in 2014. The drug was found to have a very high death rate and was not pursued further. In the early months of 2020, however, the drug was entered into COVID trials.27 Those trials were also beyond disappointing.28,29,30

Not only was the drug ineffective against the infection but it also had significant and life-threatening side effects, including kidney failure and liver damage.31 Dr. Paul Marik, a pulmonary and critical care specialist and founding member of the Front Line COVID-19 Critical Care Alliance (FLCCC), explained that during the pandemic the only drug he was allowed to prescribe was remdesivir.

When he refused to follow the remdesivir protocol, he was subjected to a "sham review," an unofficial but well-known process in which a "troublesome" doctor is accused of wrongdoing and basically railroaded out of practice. In the end, he was fired and reported to the National Practitioner Databank and the Board of Medicine.

The financial motivations to report doctors going against the grain run deep. According to Marik, the U.S. government pays hospitals a 20% upcharge on the entire hospital bill when remdesivir is used.32 Citizens Journal also reported that the U.S. government pays hospitals a "bonus" on the entire hospital bill if they use remdesivir.33 It described this practice as a bounty placed on your life, with payouts tied to declining health instead of recovery:34

"For remdesivir, studies show that 71% to 75% of patients suffer an adverse effect, and the drug often had to be stopped after five to 10 days because of these effects, such as kidney and liver damage, and death.

Remdesivir trials during the 2018 West African Ebola outbreak had to be discontinued because death rate exceeded 50%. Yet, in 2020, Anthony Fauci directed that remdesivir was to be the drug hospitals use to treat COVID-19, even when the COVID clinical trials of remdesivir showed similar adverse effects.

… We now see government-dictated medical care at its worst in our history since the federal government mandated these ineffective and dangerous treatments for COVID-19, and then created financial incentives for hospitals and doctors to use only those 'approved' (and paid for) approaches. Our formerly trusted medical community of hospitals and hospital-employed medical staff have effectively become 'bounty hunters' for your life."

Officials Push Expensive, Risky Treatments

In addition to remdesivir, Pfizer's Paxlovid was granted emergency use authorization to treat mild to moderate COVID-19 in December 2021.35 The drug consists of nirmatrelvir tablets — the antiviral component — and ritonavir tablets, which are intended to slow the breakdown of nirmatrelvir.36

But like remdesivir, there are many problems with Paxlovid. In this case, the U.S. Centers for Disease Control and Prevention issued a warning to health care providers and public health departments about the potential for COVID-19 rebound after Paxlovid treatment.37 Further, Pfizer stopped a large trial of Paxlovid in standard-risk patients because it didn't show significant protection against hospitalization or death in this group.38

Paxlovid costs $529 per five-day treatment39 and has cost U.S. taxpayers $5.29 billion,40 while safe and less expensive options exist. An investigation by Cornell University, posted on the University's preprint server January 20, 2022, found ivermectin outperformed 10 other drugs against COVID-19.41

Since the FDA and CDC cannot be trusted, and even physicians' hands are often tied by regulatory red tape, it's imperative to take responsibility for your own health. In the case of COVID-19, seek early treatment using an effective and safe protocol — not one that puts profits over patients.

 Sources and References

Restrictions in Free Range Prisons Tighten: Report Says Western Governments are Accelerating the Use of Non-Consensual Persuasion to Ensure Citizens Act and Speak in Ways Compatible w/Govt Narratives

From [HERE] Since the advent of the covid era in early 2020, Western liberal democracies have witnessed a marked acceleration in the systematic deployment of methods of non-consensual persuasion aimed at ensuring that people act and speak in ways that correspond to the dominant state-determined narrative. Throughout this period, everyone – politicians, academics, journalists, scientists and ordinary citizens – have been exposed to some combination of psychological manipulation, censorship, smearing and coercion (seehere for an overview). Disturbingly, two recent events suggest that the methods used by our government and other powerful actors to crush dissent are becoming more flagrant.

Last month, the civil liberties group Big Brother Watch published a document titled Ministry of Truth: the secret government unit spying on our speech. The report confirmed what many of us had long suspected: some of our day-to-day talk and behaviour is being covertly monitored by our own Government for any signs of deviation from their version of the ‘truth’. If the confirmation of such Orwellian activities was not alarming enough, what was arguably more striking was the scale of this state-funded enterprise. Dedicated clandestine units are embedded within a range of government departments, including: the Cabinet Office (‘Rapid Response Unit’); Digital, Culture, Media & Sport (‘Counter Disinformation Unit’); Foreign Office (‘Government Information Cell’); Home Office(‘Research, Intelligence & Communications Unit); and the Ministry of Defence (‘77th Brigade). Clearly, law-abiding citizens that say or do something that deviates from the official government line (on covid, climate change, or the war in Ukraine) risk being clocked and silenced.

Within this state-funded infrastructure to crush free speech, the activities of the ‘Counter Disinformation Unit’ (CDU) evoke particular concerns. Despite being based in the government department responsible for the processing of Freedom of Information requests, the CDU was, paradoxically, the least forthcoming with answers to transparency questions posed by Big Brother Watch. The primary aim of the CDU is to ‘monitor covid disinformation’ and to signal potentially problematic material to social media companies. The Government, via the CDU, holds “Trusted Flagger” status with social media companies while — somewhat disingenuously — claiming not to mandate platforms to remove content. This special relationship results in government concerns being more visible to platforms such as YouTube and therefore more likely to be actioned; an arm’s length mechanism for habitual state censorship.

The Big Brother Watch investigation found that the Department of Digital, Culture, Media & Sport had spent over £1 million pounds on outsourcing private companies to conduct this monitoring of social media outlets. Indeed, as described in a previous article, in summer 2021 HART itself was the victim of this dubious practice when – following an illegal hack – a commercial enterprise called ‘Logically AI’ attempted to undermine us by publicising out-of-context quotes from our informal chat logs. It was galling to discover that the UK Government was spending swathes of taxpayers’ money to monitor and smear a group of academics who were giving their time voluntarily to engage in the perfectly lawful activity of challenging some aspects of covid policy and questioning the dominant covid narrative.  

The second recent event that suggests that government methods for silencing dissent are becoming increasingly dictatorial concerns an interview Andrew Bridgen MP did with Dominique Samuels (a political commentator). The backbench Conservative, the only parliamentarian to openly express concerns about the safety of the covid vaccines, had already been suspended from the party andsmeared as being ‘antisemitic’ and part of an ‘anti-vax conspiracy’ for stating that a Jewish consultant cardiologist had told him that the vaccine rollout had been ‘the biggest crime against humanity since the Holocaust’. In the interview with Samuels, Bridgen reveals a couple of other consequences he has endured for daring to criticise the dominant narrative.

Bridgen – the democratically elected MP for North West Leicestershire – describes how he was contacted by the ‘welfare’ office at the Houses of Parliament and told that ‘a number of people had come to us to say that you were suicidal, Andrew’. He reassures Samuels that there is absolutely no basis to these concerns. Later in the interview Bridgen also discloses that, around January 2022 (in the aftermath of him submitting a letter of ‘no confidence’ in the serving Prime Minister, Boris Johnson), an advisor from number 10 messaged him to say ‘what do you want … back off and you can have anything you want’. Bridgen says he has taken screenshots of the pertinent messages to support his conclusion that ‘they tried to buy me’. [MORE]

10 Blatant Lies Parroted by Media About COVID to Induce Public Consent to Take Deadly, Experimental COVID Injections

  1. Misinformation #1: Natural immunity offers little protection compared to vaccinated immunity

  2. Misinformation #2: Masks prevent Covid transmission

  3. Misinformation #3: School closures reduce Covid transmission

  4. Misinformation #5: Young people benefit from a vaccine booster

  5. Misinformation #6: Vaccine mandates increased vaccination rates

  6. Misinformation #7: Covid originating from the Wuhan Lab is a conspiracy theory

  7. Misinformation #8: It was important to get the 2nd vaccine dose 3 or 4 weeks after the 1st dose

  8. Misinformation #8: It was important to get the 2nd vaccine dose 3 or 4 weeks after the 1st dose

  9. Misinformation #9: Data on the bivalent vaccine is “crystal clear”

  10. Misinformation #10: One in five people get long Covid

https://archive.today/2023.03.03-171938/https://nypost.com/2023/02/27/10-myths-told-by-covid-experts-now-debunked/

New Emails Show Liar Fauci Commissioned Scientific Paper to Disprove that COVID Wasn’t Made in a Lab (and that He Helped Create It)

From [HERE] New emails uncovered by House Republicans probing the COVID-19 pandemic reveal the deceptive nature of Dr. Anthony Fauci.  

They show he “prompted” or commissioned — and had final approval on — a scientific paper written specifically in February 2020 to disprove the theory that the virus leaked from a lab in Wuhan, China. 

Eight weeks later, Fauci stood at a White House press conference alongside President Donald Trump and cited that paper as evidence that the lab leak theory was implausible while pretending it had nothing to do with him and he did not know the authors.

“There was a study recently,” he told reporters on April 17, 2020, when asked if the virus could have come from a Chinese lab, “where a group of highly qualified evolutionary virologists looked at the sequences … in bats as they evolve and the mutations that it took to get to the point where it is now is totally consistent with a jump of a species from an animal to a human. 

“So, the paper will be available. I don’t have the authors right now, but we can make it available to you.” [MORE]

“Media is the Virus:” Government Building in Canada Plastered with Photos of People Killed and Injured by COVID Injections. Induced to Take Deadly Injections by Govt and Media Lies (genthanasia)

From [HERE] Watch our exclusive report of the activists plastering the CBC building on Front St. with stickers of people suspected of suffering Covid “vaccine” injuries and deaths.

Inspired by the UK’s “Media Is the Virus” protests that targeted the BBC in similar fashion, the activists hoped to share a voice for those affected while holding the CBC and other mainstream media to account for their complicity in promoting an unscientific and dangerous “safe and effective” narrative. (Bright Light News/Rumble)

UK Government Data Shows You’re Far More Likely to Die from COVID Injections than from COVID Itself

CHART IS FROM [HERE]

From [HERE] and [HERE] They apparently did not mean to do this but government officials in the United Kingdom have accidentally admittedthat the risk of death from Wuhan coronavirus (Covid-19) “vaccination” is far higher than the risk of dying from covid itself.

The data shows that eight times as many people died from the lethal injections in the six-month period following the launch of Operation Warp Speed than died from “covid” over the course of 18 months starting in March 2020.

Now that the cat is out of the bag, it is abundantly clear that Fauci Flu shots never should have been allowed to stay on the market. Had government officials been honest from the beginning about all this, thousands, if not millions, of lives could have been saved.

To tell the truth, though, would have cut into Big Pharma’s bottom line – and we simply cannot have that. Money is the only thing that matters to the pharmakeia-peddling globalists that are using these deaths jabs to cull the masses. (Related: The reason they’re not conducting autopsies on post-jab dead bodies is because they know it would expose the “vaccine” scam.)

Just about everything we were told concerning covid was a lie

Another thing the data shows is that government officials were lying about covid deaths. The vast majority of these deaths were actually caused by other things such as dementia, chronic kidney disease, chronic pulmonary disease, chronic neurological disease, and heart disease – but instead, they blamed “covid.”

This further skewed the numbers, at least early on, to suggest that “covid” is the real threat and that the “vaccines” help to minimize that threat. The reality is that the oppositeis true: “covid” is nothing to worry about, but the jabs certainly are.

“When you consider that testing was compulsory in hospitals, despite it not being written in law, and they used the PCR test notorious for producing false positives, it’s not hard to see how the Government managed to mix tens of thousands of people who actually died of other causes into the Covid-19 death statistics,” reported The Exposé about this fudging of the numbers.

It took a lot of inquiries, including numerous Freedom of Information requests, to get to the bottom of this deception. It also took an independent analysis and assessment of the data to reach an accurate conclusion about the true primary cause of death throughout the scamdemic: the “vaccines.”

The latest dataset published on Feb. 21, 2023, confirms that covid jabs massively increase a person’s risk of death – by 276 percent, in fact. Mortality rates among the unvaccinated, meanwhile, are the lowest out of every demographic.

“As I see it now that we know the consequences for all untried, untested and unproven vaccines, if any medically trained person tries to stick me with a needle, he or she will accidentally get a broken neck,” one incensed commenter wrote in response to the news.

“It is no more than intentional state-sponsored murder to apply anything like these covid vaxxes again, and the vaxxed to me are too stupid to somehow realize the vaxx and boosters are going to save them. That is also why I should not have to pay anything for this! The vaxxed knowingly injected themselves and should pay for their own healthcare going forward.”

Another commenter expressed worry that perhaps “chemtrails,” which are produced during geoengineering spraying operations, are laced with covid or some other toxic chemical designed to sicken whoever breathes them.

“In Yorkshire U.K., we are chemtrailed on a regular basis,” this person wrote. “There should be a culling of all useless MPs.”

Gullible Black Man Who Took 9 Deadly, Experimental COVID Injections is Now Undergoing Chemo, Trying to Stay Alive [yup, good luck mf]

Jim Crenshaw reports, “I guess he does not count cancer as a side effect?
He is now having or had a Cytokine Storm. What this is if you do not know is:

A cytokine storm occurs when your immune system releases too many molecules called cytokines. These molecules promote inflammation and can overstimulate the activity of other immune cells.

It is hard at work killing him. It looks like they are carving this poor dude up like a Christmas Turkey. His medical bills have lots of comma's I am sure. They cannot wait until he dies so they can list it as a covid death and really cash in.” 

"With all My Heart:" Another Canadian Puppetician Apologizes for Deadly COVID Shot Mandates [here Apologize Means ‘to Trick, to Lay the foundation for a Future Offense’ or to Reform One's Image]

According to FUNKTIONARY:

apologize – to lay the foundation for a future offense or affront. (See: Apologease, Forgiveness & Acceptance)

apology – a plea bargain in disguise. An apology is needed wherever there is no communion, contact or relationship; the “other” is a stranger. Explanation is needed because there is no love. Explanation is a trick to avoid conflict; apology is a device to avoid conflict. Apology is a trick—applied as an anger solvent—you need not be authentic in your apology as it is merely a social device (gesture) to detonate anger. Apologies, like excuses, are not for the benefit of the one to whom they are made, but the one who makes them. Apologizing does not always mean that you are wrong and the other person is right. It simply means that you value your relationship more than your ego. When there is no relationship and no love, both an apology and explanation is expected. When the other cannot understand, only then is apology needed. And if love cannot understand, what good is apology going to do? (See: Explanation, Rationalization, Forgretful, Forgiveness, Excuse, Promise, Regret, Rationalization, Anger, “Other” & Stranger)

biocide – the attempted annihilation of all life, which is the intent of Doggy and CrimethInc. (See: Doggy & CrimethInc.)

The Mask Mandates Did Nothing. Will Any Lessons Be Learned?

From [HERE] But whatever the reason, mask mandates were a fool’s errand from the start. They may have created a false sense of safety — and thus permission to resume semi-normal life. They did almost nothing to advance safety itself. The Cochrane report ought to be the final nail in this particular coffin.

There’s a final lesson. The last justification for masks is that, even if they proved to be ineffective, they seemed like a relatively low-cost, intuitively effective way of doing something against the virus in the early days of the pandemic. But “do something” is not science, and it shouldn’t have been public policy. And the people who had the courage to say as much deserved to be listened to, not treated with contempt. They may not ever get the apology they deserve, but vindication ought to be enough.

White Liberal Boulder County Authorities Target Latinos with Fear Campaign to Coerce and Induce Parental Consent for Dangerous COVID Injections for Young Kids

From [HERE] A Boulder County Public Health (BCPH) campaign to persuade parents — especially Latinos — of children ages 0 to 11 to vaccinate their kids for COVID-19 has some of the Colorado county’s parents up in arms.

The BCPH in May 2022 hired Godot, a “creative” consulting agency, to conduct focus groups and develop the campaign.

The agency’s final report — dated October 2022 and obtained in January by local citizen’s group No Vax Mandates Colorado through numerous Colorado Open Records Act (CORA) requests — describes the agency’s findings and lays out a proposed ad campaign strategy to convince the “vaccine-hesitant” to give their small children the shot.

According to the report, “Vaccine hesitancy is not binary.” So the consultants set out to characterize people on a spectrum, from “anti-vaccine” to “vaccine champions” in order to identify those individuals who may be susceptible to “moving the needle” toward having their young children vaccinated through an effective advertising campaign.

Cindy Baker, a member of No Vax Mandates Colorado for months has been trying to foster a dialogue about the project with BCPH at public meetings.

Baker told The Defender:

“The report is egregious and offensive on many levels. It defines anyone who questions mRNA injections as ‘intentionally ignorant’ and ‘selfish.’

“It aims for innovation but instead comes across as a mishmash of vicious stereotyping, vagueness on detail (such as methodology), Zoom-class arrogance and outright weirdness.”

Much research and many organizations across the country have been dedicated to understanding and overcoming “vaccine hesitancy” — particularly among Latino people — often framing it as a way to fight racial and economic injustice.

The medical establishment often blames this “hesitancy” on factors like “misinformation” and past trauma, claiming these and other issues confuse people’s thought process — instead of acknowledging that some people reject the vaccines on the basis of informed decision making.

According to Colorado’s COVID-19 tracking website, over 85% of white Coloradans have received at least one dose of the COVID-19 vaccine, but less than 50% of Hispanics have — the lowest rate for all racial/ethnic groups.

Approximately 26% of children ages 0 to 9 in Colorado have received at least one shot. Among children ages 11 to 18, that number rises to almost 59%.

The county’s program appears to be moving forward despite a broader trend where local, state and national governments are abandoning vaccine mandates and changing vaccine recommendations for young people.

For example, last month, California dropped its planned vaccine mandate for school-age children. Sweden stopped vaccinating children under age 12. The U.K. no longer recommends COVID-19 boosters for healthy people under age 50.

Despite this trend, the Centers for Disease Control and Prevention (CDC) last month added COVID-19 vaccination to its routine immunization schedule for children and adults.

The report: empathetic, fear-based messaging?

The Godot report described the findings from an unknown number of English and Spanish language focus groups the agency conducted, “exploring the web of influence, emotion, information, and misinformation behind the community’s decision making.”

The document said BCPH had little direct input on the focus groups process, but also that the process between the consultancy and BCPH was “deeply collaborative.”

Godot conducted focus groups with “community members” who were “hesitant” or had questions about vaccines. The goal was “to use empathy and trauma-informed listening skills to translate that feedback into meaningful and truthful messaging that connects with community members.”

Godot focused on communities with “lower full vaccination rates,” and said that vaccination rates among the Spanish-speaking population were lower than that of white adults and their older children in Boulder.

They recruited participants, who were compensated with a $40 gift card, by working with Latino organizations such as El Centro Amistad, which also advertised on Radio La Ley, and at a Latino-focused head start program and food bank.

The agency also had support from Out Boulder County, a client listed on the agency’s website.

The focus groups were held on Zoom due to lack of interest in attending in-person events.

The report did not include details about the number of participants or the number of focus groups conducted, questions asked, metrics for evaluating outcomes or other methodological details.

Marti Hopper, a member of No Vax Mandates Colorado, pointed to the vagueness of the project description in a statement at the Feb. 13 County Board of Public Health meeting.

“I found it very odd that the report has no methodology section. Missing completely is information on how many focus groups were conducted? What was the final make-up of the groups? Who conducted the groups, what questions were asked, what materials were handed out, etc.”

To select participants and analyze their responses, Godot said it worked with BCPH to develop a spectrum of vaccine hesitancy “based loosely on the work and thinking done by the SAGE working group within the World Health Organization.”

SAGE is the World Health Organization’s Strategic Advisory Group of Experts working Group on COVID-19 Vaccines.

SAGE researchers, such as Yale University’s Dr. Saad Omer, have conducted extensive research on “combating vaccine hesitancy” through “tailored message campaigns,” the Defender reported.

Omer is one of many prominent voices in what is known as the field of “infodemiology,” which seeks to limit the circulation of “misinformation” and “disinformation” with respect to vaccines.

Rather than conveying factual evidence to support claims, such research is dedicated to developing messaging designed to persuade people to act in particular ways.

In that spirit, Godot’s spectrum placed people into one of seven categories on a visual chart found in the report.

These categories ranged from the green-colored “vaccine champion” who expresses “outspoken support for immunizations” to the red-colored “anti-vaccine,” defined in the report as: “outspoken, intentional misinformation. Conclusions based on disproven data. Holding beliefs commonly tied to other conspiracies.”

The agency’s target group of people who could potentially be moved by an advertising campaign range from the orange-colored “vaccine resistant” type — characterized by: “statements rooted in intentional ignorance. Foundation of fact vs. fiction is generally not sound. Vocal” — to the light green-colored “vaccine compliant” type who is “willing to get vaccines to access school, work, activities OR are choosing to follow their own vaccine schedule.”

Godot said its role in the focus groups was to “reinforce the core messaging coming from the CDC and WHO,” and to find locally specific themes they could address “truthfully, genuinely, and with empathy.”

To that end, the agency came up with three themes — Knowing the Unknown, Ecosystem, and Ambivalence — and sought to develop “fear-appealing” messaging tied to each theme.

The report explained that the fear-based approach was based on Kim Witte’s Extended Parallel Processing Model (EPPM), also known as the Threat Management or Fear Management model.

According to Witte’s foundational work in this field, “Fear appeals are persuasive messages designed to scare people by describing the terrible things that will happen to them if they do not do what the message recommends.”

The U.S. Agency for International Development also uses this method and describes its logic:

 “The degree to which a person feels threatened by a health issue determines his or her motivation to act, while one’s confidence to effectively reduce or prevent the threat determines the action itself.”

The report concludes with the example of “concept boards” for the potential direction of the advertising campaign.

Several images include a large orange ball that signifies different things in different ads. Another image contains a picture of a wombat’s head on a person’s body. As they explain in the document, the proposals are often intentionally counterintuitive and avoid facts about COVID-19 in a way that is meant to be tied to the fear-appeal model.

The document states:

“These treatments get a little strange, even unintuitive. Beyond the visual intrigue and clickability, the quirkiness here is intentional. It’s a way of softening the push and pull of the EPPM. It makes them feel created for people rather than populations.

“And by not diving too deeply into the hard facts of COVID-19 vaccinations and kids, we keep their thinking high-level and empathetic, understanding that when it comes to a more foundational, global message, the national organizations continue to provide excellent material.”

The Spanish text contains errors that make the Spanish-language examples more difficult to understand.

Trying to communicate with public health policymakers ‘feels like a brick wall’

The report was brought to light through the efforts of some members of the citizen group No Vax Mandates Colorado who told their story to The Defender.

Concerned by the adverse effects of ongoing public health policy regarding COVID-19 in schools, at the University of Colorado and for the general population in Boulder County Colorado, members of the group began attending the monthly BCPH zoom meetings.

When BCPH announced its plan at the May 2022 meetingIndira Gujral, a spokesperson for BCPH said, “For younger children we see some disparities particularly by race and ethnicity that we are concerned about.”

Gujral added:

“The goal is to be able to glean information from vaccine-hesitant parents and as to what would make them feel further confident to move them along the continuum.

“We know that we have a unique population and community in Boulder, and so it’s an opportunity for us to learn and hear from parents about what their concerns are.”

At the June meeting, several citizens gave public comments, voicing their concerns about the program. They presented data on natural immunity, on the limited efficacy for vaccines among children and on vaccine injury among young people.

They argued that experimental vaccines could not be mandated and, legally, people must be apprised of all of the risks and benefits of experimental medicines.

They implored local health officials to respond to their question: “What are your reasons for promoting COVID vaccines for kids and on what scientific and ethical considerations are these policies based?”

Comments were made in “public comments” sections of the meetings, where commenters had three minutes to make their comments. There was no official response.

At the next several meetings, members of the group continued to voice their concerns.

Aware that the focus groups had been ongoing, No Vax Mandates Colorado requested documentation of the focus group findings in October 2022, along with other information about the project, including cost and funding sources from the BCPH.

They made a CORA request, which is similar to a Freedom of Information Act request, but at the state level.

According to No Vax Mandates Colorado, BCPH told them there would be a cost of over $700 to respond to their request. Public agencies are permitted to charge for search time and review time on their requests.

The group said they narrowed their request substantially, but BCPH still required fees of several hundred dollars, which they found prohibitive.

After making four requests, BCPH informed them in December the summary document would be available in mid-January.

BCPH sent them the document — dated October 2022 on the cover, but dated “Final-1-20-23” in pdf itself — in late January and also posted it on its website. [MORE]

Google Hides Patent Data Showing Rothschild was Involved in COVID-19 Testing Since 2015

From [HERE] Compare the two following screenshots. The first screenshot shows the Google Patents publication of a system and method for testing for covid-19, dated 18 August 2022, which is also mentioned in our book Hope Amidst a Tsunami of Evil.

The second screenshot (from 21 February 2023) shows the same entry with some changes which have been made after September 2022.

Same link—two different versions.

Spot the differences: Image 1) shows the year 2015. Rothschild is stated as the applicant in 2020.

Image 2) begins with the application made in 2020 after the pandemic began. The name Rothschild is left out.

Accessed 18 August 2022:

[MORE]