Cloutlaws Bill Gates and Pfizer CEO Sued Over COVID Lies: Netherlands Ct Advances Injured Plaintiffs' Claim the Public was Intentionally Misled about the Safety of COVID Shots-Makers Hid Known Dangers

According to FUNKTIONARY:

cloutlaw – any member of the Overruling Overclass who covertly schemes or overtly acts without impunity and sans accountability (above the Lex and below the radar of jurisprudence). 2) the financial juice (if caught) to get let loose (get acquitted). 3) the jet set—set free from accountability. 4) the necessary pull to pull oneself out of deep-dish trouble.

From [HERE] A Netherlands court last week ruled that Bill Gates can stand trial in the Netherlands, in a case involving seven people injured by COVID-19 vaccines.

According to Dutch newspaper De Telegraaf, the seven “corona skeptics” sued Gates last year, along with former Dutch prime minister and newly appointed NATO Secretary General Mark Rutte, and “several members” of the Dutch government’s COVID-19 “Outbreak Management Team.”

Other defendants include Albert Bourla, Ph.D., CEO of Pfizer, and the Dutch state.

“Because Bill Gates’ foundation was involved in combating the corona pandemic, he has also been summoned,” De Telegraaf reported.

According to Dutch independent news outlet Zebra Inspiratie, the plaintiffs allege that Gates, through his representatives, deliberately misled them about the safety of the COVID-19 shots, despite knowing “that these injections were not safe and effective.”

Dutch independent journalist Erica Krikke told The Defender that the seven plaintiffs — whose names are redacted in the lawsuit’s publicly available documents — “are ordinary Dutch people, and they have been jabbed and after the jabs they got sick.”

Krikke said that of the seven original plaintiffs, one has since died, leaving the other six plaintiffs to continue the lawsuit.

The lawsuit was filed in the District Court of Leeuwarden. According to De Telegraaf, “Gates had objected because, according to him, the judges did not have jurisdiction.” Accordingly, the court first “had to rule in the so-called incident procedure,” De Andere Krant reported.

Zebra Inspiratie reported that the hearing in this “incident procedure” took place on Sept. 18 and that Gates’ representatives disputed jurisdiction, but not the claim.

According to De Andere Krant, Gates was represented by the Pels Rijcken law firm, based in The Hague, described as “the largest and the premier litigation law firm in the Netherlands.” Gates did not appear at the Sept. 18 hearing, but attorneys for Gates argued that the court “had no jurisdiction over him because he lives in the United States.”

However, in its Oct. 16 ruling, the Leeuwarden court ruled it does have jurisdiction over Gates. De Andere Krant reported that the court found “sufficient evidence” that the claims against Gates and the other defendants are “connected” and based on the same “complex of facts.”

Other defendants who reside outside of the Netherlands, including Bourla, did not challenge the court’s jurisdiction.

The court ruled Gates must pay attorneys’ fees and additional legal costs totaling 1,406 euros (approximately $1,520). A hearing is scheduled for Nov. 27.

Study of 1.7 Million Kids and Teens Who Got Pfizer COVID Injections Found Myopericarditis Only in Vaxed Groups

From [HERE] The Pfizer-BioNTech COVID-19 vaccine provided children and teens in England with only about 14 to 15 weeks of protection against testing positive for the virus, according to a preprint study of over 1.7 million children ages 5 to 15 in the English National Healthcare System (NHS).

Researchers investigating the safety and effectiveness of Pfizer’s vaccine in fully vaccinated, partially vaccinated, and unvaccinated children and teens, also found cases of myocarditis and pericarditis only in vaccinated children.

“This study clearly shows that Pfizer’s COVID vaccine provides almost no benefit to children and adolescents, but does increase their risk of myocarditis and pericarditis,” said Brian Hooker, Ph.D., chief scientific officer of Children’s Health Defense. “It begs the question: Why does the CDC continue to recommend these unlicensed shots for kids? Where is the data they use to support their statement that the benefits of these vaccines outweigh the risks?”

The study found that vaccinated children required slightly fewer emergency room visits and hospital stays, but that those outcomes were extremely rare in children and teens across all groups.

There were no COVID-19 deaths among any of the study subjects.

Public health agencies in the United Kingdom (U.K.) and in the U.S. granted authorization to the Pfizer vaccines based on clinical trials that measured immunogenicity — or how well the vaccine elicited an immune response in the body — and efficacy against infection.

The trials didn’t test how well the vaccines protected against severe disease. They also didn’t assess particular safety endpoints, like myocarditis and pericarditis, which have been reported globally. [MORE]

State Department Colluded With Social Media to Censor Content, Twitter Files Show

From [HERE] The latest release of the “Twitter Files” includes evidence that the U.S. Department of State worked closely with social media platforms, despite denials by government officials.

Independent journalist Paul D. Thacker published the documents today in The Disinformation Chronicle. Thacker’s previous “Twitter Files” installments revealed evidence of collusion between the federal government, social media platforms and private actors to censor content.

According to Thacker, the newly released documents add to existing evidence that the Biden administration worked closely with platforms like Twitter to censor content and influence social media content moderation policies.

“These emails [call] into sharp question claims by Democrats and their allies in the media that Twitter did not collude with federal agencies and was free from Biden administration pressure to make its own censorship decisions,” Thacker wrote.

According to the new “Twitter Files,” the Indian government pressured Twitter to censor accounts in 2021, including accounts critical of India’s COVID-19 policies.

This led Twitter to hire Albright Stonebridge, a lobbying firm “closely aligned with the Biden administration” — and previously funded by the Bill & Melinda Gates Foundation — to pressure the State Department for assistance.

“Around this same timeframe, emails show that the State Department was pressuring Twitter to censor accounts they didn’t like,” Thacker wrote.

Thacker told The Defender the Indian government “was going after Twitter for not suspending accounts critical of the government, and there were threats that Twitter employees in the country would be arrested.”

The State Department then began “working closely with Twitter to deal with the company’s problems in India,” Twitter’s third-largest market, at the same time that it “was leaning on Twitter to censor certain accounts and topics,” Thacker said.

The new “Twitter Files” release is the latest in a series of installments, based on internal company records, that suggest “close coordination between U.S. government officials and social media companies to censor viewpoints and accounts — often those that opposed Biden administration policies,” Thacker wrote. [MORE]

“Vaxxed 3” Recalls the SpokesPuppets who Tricked the Public Into Getting COVID Shots [Consent Obtained by Lies, Non-Disclosures or Coercion is Not Informed Consent; It's Battery, Negligence or Fraud]

Dr Yeardon and Dr Blynd: Authorities Own the Minds of Those who Believe “The COVID Lies." The False Narratives are Enemy Outposts in the Believer's Mind, Giving Rise to More Coercive Political Systems

Consent obtained by lies, halfTruths, non-disclosures, fraud, coercion is not lawful consent - it is induced consent, which is unlawful.

A plaintiff cannot ordinarily be regarded as actually consenting to the defendant's conduct if the plaintiff assented to the conduct while mistaken about the nature and quality of the invasion intended by the defendant. Likewise, an overt manifestation of assent or willingness would not be effective apparent consent if the defendant knew, or probably if he ought to have known in the exercise of reasonable care, that the plaintiff was mistaken as to the nature and quality of the invasion intended.... The decisions in this area have involved assent induced by fraud, in the sense that the defendant was either aware of the plaintiff's mistake or ignorance and failed to disclose the truth, or the defendant induced the mistake with representation which he knew was false. Prosser and Keeton on Torts § 18, at 119-20 (5th ed. 1984).

The failure to provide informed consent is a basis of medical malpractice. But it also may be the basis of a lawsuit for an intentional battery (murder), negligence or fraud.

Battery is an intentional, unwanted or offensive touching by another. A lawsuit for battery increases the likelihood of punitive damages and unlike a claim for negligence, no proof of injury or harm is necessary. A lawsuit for battery generally has a shorter statute of limitations than a claim for negligence.

There Are No Licensed COVID Vaccines for Kids Under 12 — But CDC Wants Babies to Get 3 Pfizer Shots by Age 9 Months

From [HERE] Nine-month-old babies must receive multiple doses of an unlicensed mRNA COVID-19 vaccine to be considered “up to date” with their COVID-19 vaccination, according to the Centers for Disease Control and Prevention (CDC).

The CDC’s updated guidance, issued Aug. 30, states that children — as young as 6 months old — should get either two doses of the 2024-2025 Moderna vaccine or three doses of the 2024-2025 Pfizer-BioNTech vaccine.

If getting the new Pfizer shot, the baby is supposed to receive the first dose at 6 months, the second dose three weeks later and the third dose at least eight weeks after the second dose — meaning, that by 9 months old, babies are supposed to have received three Pfizer shots.

If getting the latest Moderna shot, the CDC recommends babies get the first dose at age 6 months and the second dose a month later.

The latest Pfizer and Moderna COVID-19 shots for children under 12 are unlicensed in the U.S. The U.S. Food and Drug Administration (FDA) has granted only emergency use authorization (EUA) for the vaccines.

Children’s Health Defense (CHD) CEO Mary Holland told The Defender, “The earlier COVID shots have been proven unsafe and ineffective. Now we’re asked to believe that newer versions are miraculously safe and effective?”

“This is an insult to people’s intelligence,” she said, “I pray that parents will have the good sense to say no to these dangerous and unnecessary shots for babies.”

As of July 28, 37,814 deaths following COVID-19 vaccination had been reported to VAERS, the Vaccine Adverse Event Reporting System, run by the FDA and CDC.

Of those, 187 reports were for children and teens under 18. Nearly 13,000 reports listed the age as “unknown.”

VAERS analyst and expert Albert Benavides recently told The Defender he believes VAERS is “throttling” and underreporting deaths of all ages following COVID-19 vaccination.

Meanwhile, the CDC continues to tell the public that COVID-19 vaccines are “safe and effective.”

There’s no licensed COVID vaccine for kids under 12

There are still no licensed COVID-19 vaccines available for children under 12, Hooker said — so all COVID-19 vaccines given to young kids are EUA products.

The FDA’s website on EUA for medical products states that EUA vaccines only have to meet the standard of “may be effective” as long as if, “based on the totality of the scientific evidence, it is reasonable to believe that the product may be effective for the specified use.”

“The ‘may be effective’ standard for EUAs provides for a lower level of evidence than the ‘effectiveness’ standard that FDA uses for product approvals,” the website states.

Before a vaccine can be fully licensed, the vaccine maker typically is required to conduct numerous clinical trials to demonstrate that the product is safe. However, the safety requirements for EUA are more flexible. [MORE]

Study of 125 Countries Finds ‘No Apparent Benefit’ From COVID injections

From [HERE] A new study by a team of Canadian researchers into excess mortality during the COVID-19 pandemicfound that patterns of excess death globally could not be explained by the virus, including long COVID.

The study, by researchers with Correlation Research in the Public Interest, examined excess mortality in 125 countries during the pandemic. It found that mortality patterns correlate closely with the imposition of restrictions such as lockdowns and with the COVID-19 vaccine rollout.

The investigation determined that pandemic-related restrictions resulted in 30 million deaths globally and that 17 million deaths can be attributed to the COVID-19 vaccines.

The researchers concluded that “nothing special would have occurred in terms of mortality had a pandemic not been declared and had the declaration not been acted upon.”

Joseph Hickey, Ph.D., one of the paper’s co-authors and president of Correlation, joined “The Defender In-Depth” this week to discuss the study’s findings and analyze the likely causes contributing to increases in excess deaths and overall mortality.

Excess death data ‘not compatible’ with ‘particularly virulent special pathogen’

Hickey explained that “all-cause mortality” refers to “the number of deaths without filtering by the cause of death” during a given period, while “excess deaths” refers to “how many deaths occurred that are above and beyond what would have been predicted” for a certain period.

Hickey and the study’s co-authors analyzed pre-pandemic raw data from 2015 to 2019, and data collected between 2020 and 2023. Hickey said the data, collected from 125 countries, found “a large amount of excess deaths.”

“We calculate that over the COVID period … about 0.39% of the global population died in excess. That compares to about 0.97%” during the 1918 Spanish Flu pandemic in 1918.

Hickey said this was “the largest non-war mortality event in 100 years” globally.

The study also found patterns of excess mortality across the world were “very heterogeneous,” as they varied “significantly from country to country,” across regions within the same country and across age groups. Hickey said:

“There are some countries that immediately following the declaration of the pandemic in March of 2020 had an enormous spike in … excess mortality that is very sharp, very fast and very narrow. But that does not occur in all countries.

“There are neighboring countries that don’t have that at all. There are countries that do not have any excess mortality throughout all of 2020, and it’s only in 2021 when the vaccines are rolled out, that they suddenly have excess. And that excess can be a sharp spike, or it can be a raised and sustained plateau.”

Noting that none of the countries had any excess deaths before the declaration of the pandemic, Hickey said this finding does not match the spread of a deadly virus.

“If you take the model of a new very deadly pathogen that is spreading around the world, you should not see this very high degree of heterogeneity … it’s simply not compatible with the hypothesis of a particularly virulent special pathogen,” he said.

“If there was a specifically virulent and dangerous pathogen that was spreading around the world, it would not wait for a political declaration of a pandemic to start causing excess mortality,” Hickey added.

Instead, “a much simpler, much more elegant explanation is that it’s differences in national policies, national measures of one kind or another that are responsible for these very different outcomes in excess mortality,” Hickey said. [MORE]

American Dental Association Pledges to Push Fluoridated Water Despite Court Finding that ‘Fluoride Causes Cognitive Damage to Children’

From [HERE] A landmark federal court ruling recently determined that fluoride levels in U.S. drinking water pose unnecessary risks to children’s IQ and cognitive development, validating what conspiracy theorists have warned about for decades.

Generations of people have been poisoned through the water supply without their consent. This toxic byproduct – hexafluorosilicic acid – has been dripped into most municipal water supplies for decades. The institutions that thought they knew what was best for everyone’s dental health have instead dumbed down entire generations of people, harming their IQ and cognitive development. This widespread dumbing down of human populations helps explain the lack of critical thinking skills in the 21st century.

None of these serious matters of public health seem important to institutions like the American Dental Association, however. In fact, the ADA immediately issued a statement, doubling down and defending water fluoridation.

Biased and stubborn American Dental Association defends fluoridated water

Some institutions, like the American Dental Association, are pushing back against the science and dismissing this federal court ruling, demanding that fluoride be considered safe for everyone, against all available evidence.

The ADA, representing some 159,000 dentists across the country, posits itself as “the premier source of oral health information.” The ADA claims that they have “promoted the art and science of dentistry since 1859” while advocating for the public’s health. But the ADA aren’t thinking about the big picture with fluoride and how it is destroying the cognitive abilities of those exposed on a daily basis.

Immediately after the court’s ruling, the ADA hastily wrote:

The American Dental Association (ADA) remains staunchly in support of community water fluoridation at optimal levels to help prevent tooth decay. The district court ruling against the Environmental Protection Agency (EPA) provides no scientific basis for the ADA to change its endorsement of community water fluoridation as safe and beneficial to oral health.

The ADA called the ruling and the barrage of social media posts that followed “pseudo-scientific information.” The ADA claims that social media users are spreading information that “is not always based on research conducted according to impartial and evidence based scientific methodology.” The ADA contends that “conclusions drawn from research are not always scientifically justifiable or without bias.” One might point out that the ADA is drawing their own biased conclusions from research that was validated in court. By ignoring the latest evidence on fluoride’s damage to children’s brains, the ADA might be guilty of spreading “pseudo-scientific information.” [MORE]

Federal Court Rules Fluoride in Water Poses an ‘Unreasonable Risk’ to Children, Reduces Their IQ

From [HERE] Several U.S. cities, towns and counties announced they will stop fluoridating their water in the aftermath of a landmark federal court ruling that found water fluoridation at current levels poses an “unreasonable risk” of reduced IQ in children.

Abilene, Texas; Yorktown and Somers, New York; and the Weber Basin Water Conservancy District in Utah are among those cities and districts that responded quickly to the Sept. 24 ruling by U.S. District Judge Edward Chen.

Chen ruled the U.S. Environmental Protection Agency (EPA) can no longer ignore the risk fluoridation poses to human — especially children’s — health and that the agency must take regulatory action.

The ruling stemmed from a lawsuit filed in 2017 by Fluoride Action NetworkMoms Against FluoridationFood & Water Watch and individual parents and children. It followed the publication of a key report by the U.S. Department of Health and Human Services’ National Toxicology Program.

Rick North, board member of the Fluoride Action Network, told The Defender he expects more cities and towns to announce they will end the practice of fluoridation.

“Fluoridation is a house of cards and it’s going to fall,” North said. “It’s only a matter of when. Our job is to make the wind blow.” [MORE]

30 Lawmakers Sponsor Bill to End Liability Protection for Vaccine Makers

From [HERE] A bill introduced late last week in the U.S. House of Representatives would end the liability protections Congress gave vaccine makers under the 1986 Childhood Vaccine Injury Act.

Thirty Republican lawmakers signed on as co-sponsors to House Bill 9828, End the Vaccine Carveout Act. The proposed legislation would end the broad protection from liability for injuries resulting from vaccines listed on the Centers for Disease Control and Prevention’s (CDC) Childhood Immunization Schedule.

“The … vaccine makers are criminal enterprises that have paid tens of billions in criminal penalties over the past decade,” Children’s Health Defense (CHD) founder and chairman on leave Robert F. Kennedy Jr. said in a statement on the bill.

Kennedy, who has long advocated for eliminating liability protection for vaccine manufacturers, added, “By freeing them from liability for negligence, the 1986 statute removed any incentive for these companies to make safe products. If we want safe and effective vaccines we need to end the liability shield.”

CHD, React19 and The American Family Project also supported the development of the bill, the press release said.

REACT19 founder Brianne Dressen, who experienced a debilitating COVID-19 vaccine injury as a volunteer in AstraZeneca’s clinical trial, announced the bill and its co-sponsors in a post on X, formerly Twitter.

“People harmed are long overdue for a compensation process that actually works, and it’s time for the drug companies to pick up the tab,” she said.

‘Complex sham compensation program’ in place since 1986 act

Congress passed the 1986 National Childhood Vaccine Injury Act to address the risks of vaccines — which Congress and vaccine makers acknowledged had “unavoidable” side effects.

The act set up a “no-fault” system whereby instead of suing the manufacturers, people injured by vaccines can file a claim with the National Vaccine Injury Compensation Program (VICP), which adjudicates the claims.

The VICP was meant to insulate vaccine makers from lawsuits that could bankrupt them while ensuring that injury victims had a straightforward, non-adversarial and fair path to compensation.

The program is funded by a 75-cent-per-dose tax, paid by vaccine makers, for every vaccine included in the program.

The U.S. Department of Health and Human Services administers the VICP, also known as the “vaccine court.” Court-appointed “special masters” — typically lawyers who previously represented the U.S. government — manage and decide the individual claims.

The proceedings are more informal than a typical courtroom. There is no judge or jury, and the rules of evidence, civil procedure and discovery do not apply.

In practice, getting compensation through the VICP has been notoriously difficult. Critics say the program has devolved to protect government agencies and corporations rather than the health of vaccinated children.

CHD CEO Mary Holland said the 1986 Childhood Vaccine Injury Act effectively left parents and children injured by vaccines with no substantive way to get any compensation while giving vaccine makers a free pass.

“For over 35 years, parents of children injured and killed by government-recommended vaccines have been left with no meaningful redress — only a complex, sham compensation program that pits grieving families against the government, while Big Pharma enjoys no liability,” she said.

“During that same time, chronic health conditions in children — autism, ADHD [attention-deficit/hyperactivity disorder], severe allergies, asthma — have skyrocketed,” Holland said.

In some cases, people who are dissatisfied with the outcome of their case in the VICP, or who don’t get a timely decision, can sue the manufacturer for limited causes of action, such as fraud — as is the case in many of the over 200 gardasil injury lawsuits currently being argued against Merck in federal court. [MORE]

How Many Black Children Did Pfizer Kill with Its Drug "Oxbryta?" After Targeting Blacks, Pfizer Pulls Blood Cell Therapy Off Market Due to Deaths: Black Children Were at Greatest Risk

From [KARENKINGSTON] Pfizer targeted parents of African American children who had sickle cell disease with their OXBRYTA marketing. Yesterday, Pfizer announced OXBRYTA is being withdrawn from 35 countries due to deaths.

Immediately after the stock market closed on September 25, 2024, Pfizer announced that “it’s voluntarily withdrawing all lots of OXBRYTA for the treatment of sickle cell disease at this time, in all markets where it is approved. Pfizer is also discontinuing all active clinical trials for the drug and expanded access programs worldwide.” Sickle cell disease is a genetic disease that affects hemoglobin and the ability for red blood cells to carry oxygen causing red blood cells to ‘sickle’ or become deformed.

Per the website, OXBRYTA supports hemoglobin in order to prevent the breakdown of red blood cells.

Pfizer’s OXBRYTA marketing targeted African American parents whose children were diagnosed with sickle cell disease. [MORE]

Karen Kingston says Trump Outmaneuvered Big Pharma after being Mandated to Deliver COVID Shots. Is that Why Elites are Using Their Authorities and Media to Try to Silence and Kill Him?

From [KAREN KINGSTON] I’ve frequently been criticized for not condemning Trump for allowing the COVID-19 mRNA injections to come to market. As a former corporate executive who has written, reviewed, and negotiated well over a hundred contracts with large biopharma companies, I always asserted that President Trump had an extremely clean paper trail in regard to the Pfizer contract. 

Pfizer agreed to work independent of the US government and military in order to deliver safe and effective vaccines thereby forfeiting their derivative immunity in exchange for first-to-market and intellectual property rights in a growing multi-trillion-dollar industry.

When it came to negotiating the Pfizer contract, it appears that President Trump was not only exceptionally well-versed in the laws regulating emergency use authorized (EUA) products and U.S. laws regulating military contracts, but that he also leveraged his expertise in outsmarting and outmaneuvering unethical businessmen (aka con artists).  [MORE]

Assassin of Haitian President Linked to US Intel. Did US Authorities Murder Moïse b/c He Rejected MRNA COVID Shots? Poor Nation that Didnt Vax, Social Distance or Shut Down was Unaffected by Plandemic

From [FTP] South Florida businessman accused of funding the plot to assassinate former Haitian President Jovenel Moise received legal advice endorsing a mission to capture the head of state from a confidential informant of a US intelligence agency, court documents unveiled in July 2024 allege. According to the accused’s legal team, “the discovery received from The Government redacts the U.S. intelligence agency with which [the informant] is affiliated,” but “it is clear that he is a [confidential informant] for a U.S. Intelligence Agency.”

The businessman, Walter Veintemilla, and his company, Worldwide Capital Lending Group, stand accused of providing a $175,000 line of credit to Florida defense contractor CTU Security LLC, which reportedly carried out the assassination. 

On July 1, Veintemilla’s attorneys filed a pretrial motion to depose the alleged intelligence informant, “J.C.,” who is described as an Ecuadorian lawyer living in Bolivia. Veintemilla’s defense argues that testimony from “J.C.” would support their contention “that several investigative and administrative agencies of the United States Government were aware of the actions and intentions of his alleged co-conspirators in Haiti and supported those actions.”

Veintemilla’s co-defendants also joined in that motion to depose J.C. in Bolivia. Several of them, including Arcangel Pretel Ortiz and Antonio Intriago, were accused by the Bolivian government of plotting an aborted coup attempt in October 2020 against President Luis Arce. German Alejandro Rivera Garcia, a retired Colombian Army officer who helped lead the kill team in Haiti, was also present in Bolivia with this group. He was extradited to the US, pled guilty, and received a life sentence in late 2023. [MORE]

One week after Haiti's president was assassinated, the country's first shipment of COVID-19 vaccines finally arrived.

President Jovenel Moïse was allegedly shot a dozen times in his private residence on July 7. Prior to his murder Haiti, the poorest nation in the Western hemisphere, was the only nation that hadn’t vaccinated a single resident against Covid-19.

Haiti was among the 92 poor and middle-income countries offered doses under the Covax Facility. But the government initially declined AstraZeneca PLC shots, citing side effects and widespread fears in the population.

“Haiti did not reject the offer of vaccines from Covax,” Haiti Ministry of Health General Director Laure Adrien said in a telephone interview. “All we asked was that they change the vaccine they were providing us.” [MORE]

Boris Johnson says COVID Lockdowns were “Medieval.” Is that One of the Reasons Elites Removed Him from Service?

From [HERE] Former British Prime Minister Boris Johnson has said he doubts lockdowns played a significant role in bringing the COVID-19 pandemic to an end.

In extracts released from his new memoir Unleashed, he describes the lockdowns as “literally medieval in their savagery and consequences,” and likened himself to King Canute attempting to “repel the waves of a highly contagious disease.”

He also says he believes the COVID-19 virus did originate in a laboratory in Wuhan, rather than a wet market.

At the British government’s COVID inquiry last December, Johnson said there were “appalling harms on either side of the decision” to lock down the country, and he apologised for any mistakes he and his government made.

Initially, according to the extracts, Johnson said he believe the lockdowns were reducing the spread of the virus.

“It was only later that I started to look at the curves of the pandemic around the world—the double hump that seemed to rise and fall irrespective of the approaches taken by governments,” he writes.

“There were always two waves, whether you were in China, where lockdowns were ruthlessly enforced, or in Sweden, where they took a more voluntary approach.”

He continues: “I am not saying that lockdowns achieved nothing; I am sure they had some effect. But were they decisive in beating back the ­disease, turning that wave down? All I can say is that I am no longer sure.”

Johnson goes on to say that the lockdowns showed Britain had “barely progressed” from the Elizabethan era, four hundred years ago, when theatres were closed and the number of mourners at funerals were limited to stop the spread of pestilence.

Three national lockdowns took place in Britain, from March 2020 to June 2020, from November 2020 to December 2020 and from January 2021 to May 2021.

Boris Johnson was forced to resign in 2022, after a series of scandals including so-called “Partygate,” when it was revealed the members of the government did not abide by the social-distancing restrictions imposed on the country.

Allies of Mr Johnson, such as Michael Gove, have suggested the lockdowns went totally against the former prime ministers “worldview.”

After Using Unscientific Nonsense to Destroy Jobs and Businesses w/COVID Lockdowns, Elite White Liberals in DC to Allow Evictions of Mostly Black People to Resume w/Rollback of City Tenant Protections

From [HERE] During the pandemic, emergency legislation made it easier for people falling on hard times to obtain rental assistance and stay in their homes or apartments.

Now, D.C. leaders say some are using the changes to delay their eviction, and those delays are impacting landlords that provide affordable housing in the city.

“The long-term continuation of these emergency policies, some of them becoming permanent policies, have put the affordable housing that we have invested so heavily in at risk, ” said D.C. Mayor Muriel Bowser at a press conference on Monday.

Bowser joined D.C. Council Chair Phil Mendelson to announce emergency legislation that both said would roll back the Emergency Rental Assistance Program, or ERAP, to where it was before the pandemic.

The D.C. Council will take up the emergency legislation Tuesday, and Mendelson believes there is enough support among council members for the measure to pass.

Mutombo Dead from Tumor. Tricked by Gov Liars Into Taking COVID Shot and Spreading Myth-Information on Deadly Injections. Coincidence Theorists call Silence on Mounting Deaths 'Respect for the Family'

PROLIFIC SHOT BLOCKER CAN’T DODGE THE MRNA DEATH SHOT. Dikembe Mutombo has died at 58, the NBA announced on Monday. The cause of death was brain cancer. [MORE] On Oct 15, 2022 ESPN reported that Mutombo began receiving treatment for a brain tumor.

Ironically, Dikembe helped to propagandize deadly COVID shots by spreading unscientific nonsense and myth information. [MORE] and [MORE] and [MORE] Similar to “Race,” COVID Shots are a Leading Cause of Millions of Coincidences. Racists and synchronized, obedient Defenders of Genocidal, Coerced Shots Dogmatically Disagree.

According to FUNKTIONARY,

coincidence theories – the naïve belief that problems (and solutions to them) happen spontaneously, that nothing is ever foreseen, plotted, planned or conspired through collusion by the wealthy and powerful. (See: Pathocracy, Fronts, Predictive Programming, Conspiracy Theories, Laws, Technetronic Age, WARS & Council on Foreign Relations).

According to Dr. Michael Palmer and Dr. Sucharit Bhakdi:

Are mRNA vaccines dangerous in principle, or is the observed harm accidental?

The facts presented in this book will make it clear that the COVID-19 mRNA vaccines have done very significant harm. We might wonder whether this damage was caused by these vaccines working as intended, or rather by undeclared ingredients or contaminants. This question cannot be dismissed out of hand. Several kinds of contaminations have been clearly documented; and furthermore, there is an unusually large spread in the rate of adverse events between batches of the same COVID-19 vaccines, which indicates at the very least that these were not manufactured to consistent standards (see Section 5.4). Each of these factors may potentially influence toxicity. However, we will make the case that most of the observed severe harm is best understood in terms of these vaccines doing what they are designed to do; the harm is not accidental but rather built into the mRNA technology.

1.2 COVID-19 vaccines were never about your health

The official story of the COVID-19 “pandemic” is a staggering concoction of unscientific nonsense and outright lies [2]. This started already with the tales about the allegedly natural origin of the SARS-CoV-2 virus, which became untenable as soon as Chinese virologist Li-Meng Yan and her colleagues published their detailed analysis of the viral genome, revealing unambiguous traces of laboratory manipulation [3, 4]. While we still don’t know for certain who was or was not involved in the creation of this chimeric virus, this question is not really crucial: the absurd and predictably harmful “response measures”, which were imposed swiftly and in lock-step by the WHO and by most national governments of the world, revealed clearly and early on that the virus and these measures were part of the same agenda. Already in early 2020, Klaus Schwab and Thierry Malleret, in their book COVID-19: The Great Reset [5], spelled it out for us:

The worldwide crisis triggered by the coronavirus pandemic . . . is bringing economic disruption of monumental proportions. . . . At the time of writing (June 2020), the pandemic continues to worsen globally. Many of us are pondering when things will return to normal. The short response is: never.

The authors’ patently false claim that the “pandemic continues to worsen” as of June 2020—see for example Figure 1.1—gives the game away: Klaus Schwab and his cronies at the World Economic Forum are using COVID-19 as a cudgel to inflict upon the world their premeditated “economic disruption of monumental proportions” and to usher in their dystopian “new normal.” Early measures such as the closure of small businesses, schools, and places of worship caused grave damage to our livelihoods and our quality of life.

However, even worse was to come with the introduction of the gene- based COVID-19 vaccines. While there is now overwhelming evidence of grave injury and death due to these products (see Chapters 4 and 7), this evidence is still only slowly making its way into general awareness. A case can be made that these risks were not merely accepted but intended; the entire process of development and approval appears to have been designed to conceal the dangers and rush these harmful vaccines to market. [MORE]