Illegal Collusion Between Government and Big Tech Exposed
By Dr. Joseph Mercola | September 15, 2022
In a September 1, 2022, article,1 the Post Millennial reveals how federal officials in the Biden administration have held secret censorship meetings with social media companies to suppress Americans’ First Amendment rights to free speech, and to ban or deplatform those who share unauthorized views about COVID and vaccines.
The evidence for this comes out of a lawsuit2 brought by the New Civil Liberties Alliance and the attorneys general of Missouri and Louisiana (Eric Schmitt and Jeff Landry) against President Biden, filed in May 2022.
During the discovery process, the plaintiffs sought to identify “all meetings with any social media platform relating to content modulation and/or misinformation,” which is how we now know that such illegal meetings did, in fact, take place.
Illegal Collusion to Suppress Free Speech
Monthly, a Unified Strategies Group (USG) meeting took place — and may still be taking place — between a wide variety of government agencies and Big Tech companies, during which topics to be censored and suppressed were/are discussed.
Censored topics included stories involving COVID jab refusal, especially those involving military refusals and consequences thereof, criticism against COVID restrictions and their effects on mental health, posts talking about testing positive for COVID after getting the jab, personal stories of COVID jab side effects, including menstrual irregularities, and worries about vaccine passports becoming mandatory.3 According to the New Civil Liberties Alliance:4
“… scores of federal officials … have secretly communicated with social-media platforms to censor and suppress private speech federal officials disfavor. This unlawful enterprise has been wildly successful.
Under the First Amendment, the federal government may not police private speech nor pick winners and losers in the marketplace of ideas. But that is precisely what the government has done — and is still doing — on a massive scale not previously divulged.
Multiple agencies’ communications demonstrate that the federal government has exerted tremendous pressure on social-media companies — pressure to which companies have repeatedly bowed …
Communications show these federal officials are fully aware that the pressure they exert is an effective and necessary way to induce social-media platforms to increase censorship. The head of the Cybersecurity and Infrastructure Security Agency even griped about the need to overcome social-media companies’ ‘hesitation’ to work with the government …
This unlawful government interference violates the fundamental right of free speech for all Americans, whether or not they are on social media. More discovery is needed to uncover the full extent of this regime — i.e., the identities of other White House and agency officials involved and the nature and content of their communications with social-media companies.”
Jenin Younes, litigation counsel for the New Civil Liberties Alliance added:5
“If there was ever any doubt the federal government was behind censorship of Americans who dared to dissent from official COVID messaging, that doubt has been erased. The shocking extent of the government’s involvement in silencing Americans, through coercing social-media companies, has now been revealed …”
Federal Agencies Involved in Free Speech Suppression
Documents obtained so far have identified more than 50 federal employees across 15 federal agencies, who participated in these censorship meetings or otherwise engaged in illegal censorship activities.6 This includes officials from:
- The Cybersecurity and Infrastructure Security Agency’s (CISA) Election Security and Resilience team
- Department of Homeland Security’s (DHS) Office of Intelligence and Analysis
- The FBI’s foreign influence taskforce
- The Justice Department’s (DOJ) national security division
- The Office of the Director of National Intelligence
- White House staff (including White House lawyer Dana Remus, deputy assistant to the president Rob Flaherty and former White House senior COVID-19 adviser Andy Slavitt)
- Health and Human Services (HHS)
- Centers for Disease Control and Prevention (CDC)
- National Institutes of Allergy and Infectious Diseases (NIAID)
- The Office of the Surgeon General
- The Census Bureau
- The Food and Drug Administration (FDA)
- The State Department
- The U.S. Treasury Department
- The U.S. Election Assistance Commission
Emails from a strategic communications and marketing firm called Reingold7 also reveals that outside consultants were hired to manage the government’s collusion with social media to censor Americans. For example, Reingold set up a “partner support portal” for the CDC so that CDC officials could link emails to the portal for easier flagging of content it wanted censored by social media companies linked to the portal.
Big Tech Companies Involved in Government Censorship
On the private industry side, notable tech participants in the censorship meetings include:
- YouTube
- Microsoft
- Verizon Media
- Wikimedia Foundation
While some social media companies may have “hesitated” to censor on the government’s behalf at times, Facebook was certainly an eager beaver from the get-go. As early as February 2020, Facebook CEO Mark Zuckerberg was in contact with the State Department, offering its services to help “control information and misinformation related to coronavirus.”8
Biden Administration’s ‘Executive Privilege’ Denied
As you might expect, the White House has not cooperated with discovery and have fought to keep communications secret — especially with regard to Dr. Anthony Fauci’s correspondence — claiming all White House communications as “privileged.”
However, executive privilege does NOT apply to external communications, so the plaintiffs called on the U.S. District Court for the Western District of Louisiana to “overrule the government defendants’ objections and order them to supply this highly relevant, responsive and probative information immediately.”
September 7, 2022, Judge Terry Doughty did just that. The Biden administration’s claim of executive privilege was rejected and Doughty ordered the White House to hand over any and all relevant records.9 That includes correspondence to and from Fauci, White House press secretary Karine Jean-Pierre and many others. According to the judge’s order, they have three weeks to comply.
Examples of Illegal Government Censorship
On Twitter,10 Missouri AG Schmitt has shared a long list of examples of government censorship, including one document in which Clarke Humphrey, COVID-19 response digital director at the White House, asked Facebook to take down the Instagram account “anthonyfauciofficial,” a parody account dedicated to making fun of Fauci.11 Facebook complied.
Schmitt also shared emails12,13 between a senior Facebook official and the surgeon general, stating, “I know our teams met today to better understand the scope of what the White House expects from us on misinformation going forward.” This email came on the heels of the surgeon general’s July 2021 “misinformation health advisory.”
The CDC also coordinated with Facebook, providing them with talking points to debunk various claims, including the claim that spike protein in the COVID shots is dangerous and cytotoxic. In a July 28, 2021, email, a CDC official provided Facebook with the following counter-narrative, taken straight from the “How mRNA Vaccines Work” section on the CDC website:14
“Messenger mRNA [sic] vaccines work by teaching our cells to create a harmless spike protein …” (Emphasis in the original.)
Fast-forward to mid-June 2022, and the CDC was suddenly less sure about the harmlessness of the spike protein.
Up until then, the words “harmless spike protein” had always been bolded, but in this June revision, they removed the bolding, along with an entire section in which they’d previously claimed that mRNA was rapidly broken down and spike protein did not last more than a few weeks in the body.15 Clearly, the truth was catching up to them and certain lies were getting too risky to hold on to.
CISA also reached out to Google, Meta (Facebook’s parent company), Microsoft and Twitter for help, shortly after the DHS’s Disinformation Governance Board was announced.16 Fortunately, public outcry put an end to this Orwellian Ministry of Truth before it got started.
When Censorship Becomes Election Interference
According to The Washington Times :17
“Details about the Biden administration’s conduct raised the hackles of Republican lawmakers. ‘Confirming that this is the most dangerously anti-free speech administration in American history AND that Facebook … is nothing but an appendage of the deep state,’ Sen. Josh Hawley, Missouri Republican, said on Twitter as he shared news of the court filing.”
Other lawmakers are also getting involved. In an August 29, 2022, letter18,19 to Attorney General Merrick Garland and FBI Director Christopher A. Wray, Republican Sens. Charles E. Grassley of Iowa and Ron Johnson of Wisconsin requested records of the government’s contacts with social media companies to ascertain whether the FBI and/or DOJ did, in fact, instruct them to censor information about the Hunter Biden laptop scandal by falsely referring to it as “Russian disinformation.”20
Zuckerberg has also been asked21 to provide any correspondence involving the censorship of the Hunter Biden laptop story, especially as it pertains to the FBI’s instructions to censor this political hot potato — something he openly admitted in a recent Joe Rogan interview (see video above).22
Lawmakers Pursue Legislation to Penalize Gov’t Censorship
Three Republican House Representatives on the House Oversight and Reform, Judiciary, and Commerce committees — Reps. James Comer of Kentucky, Jim Jordan of Ohio, and Cathy McMorris Rodgers of Washington — have also introduced the Protecting Speech from Government Interference Act23 (HR.8752), aimed at preventing federal employees from using their positions to influence censorship decisions by tech platforms.
The bill would create restrictions to prevent federal employees from asking or encouraging private entities to censor private speech or otherwise discourage free speech, and impose penalties, including civil fines and disciplinary actions for government employees who facilitate social media censorship.
While the U.S. Constitution clearly forbids government censoring and restricting free speech, HR. 8752 could be a helpful enforcement tool, as people might tend to think twice when they know there’s a real and personal price to pay.
Sources and References
- 1, 3, 8 Post Millennial September 1, 2022
- 2 State of Missouri and State of Louisiana Against President Joseph Biden, Civil Action No. 22-cv-1213
- 4, 5 New Civil Liberties Alliance September 1, 2022
- 6 NTD September 1, 2022
- 7 Reingold
- 9 Washington Times September 7, 2022
- 10, 13 Twitter Eric Schmitt September 1, 2022 thread
- 11, 16, 17, 20 Washington Times September 1, 2022
- 12 Twitter, Eric Schmitt, Emails Between FB and SG
- 14 Ago.mo.gov CDC emails to Facebook July 2021
- 15 AIER September 1, 2022
- 18 Chuck Grassley Letter to Garland and Wray August 29, 2022
- 19 Chuck Grassley August 30, 2022
- 21 Chuck Grassley Letter to Mark Zuckerberg August 29, 2022
- 22 Spotify Joe Rogan Experience, Episode 1863
- 23 HR 8752 — Protecting Speech from Government Interference Act
How many Americans have gotten their second booster?
By Meryl Nass, MD | September 5, 2022
7%. Seven percent. SEVEN PERCENT! Americans have said, “No more.” And so the authorities are trying a new con job to get more of us to offer our arms. The new improved version that the government and manufacturers were too scared to test! How many times do they think they can fool you?
In its article on the new booster authorizations last Wednesday, the WaPo had quotes from Peter Hotez and Michael Osterholm, both huge vaccine supporters. Neither was happy about the rush to get the boosters out before any human testing had been done.
Neither the WaPo nor the NY Times nor most other media bothered to tell their readers that the FDA had refused to convene an advisory committee meeting so the public could see the evidence for the boosters and hear a discussion about them. They must have been instructed what to leave out.
The claim is that flu shots get grandfathered in each year with minor tweaks, so why not COVID shots? Here’s why:
- Flu shots have been around for decades and their differences from year to year are well understood
- Flu shots are used first in the southern hemisphere, so the US actually gets the benefit of six months of data before using them
- But the HUGE difference is that flu shots are licensed! They have liability! You can apply to the vaccine injury compensation program for damages. You get a legal hearing with a “special master’“ judge. The new COVID boosters are unlicensed, have no quality standards they are required to meet, and the manufacturers and government are off the hook if anything goes wrong
They fooled us enough. This time it’s shame on me.
Fauci’s Red Guards: Lawsuit Reveals Vast Federal Censorship Army
By Michael P Senger | The New Normal | September 2, 2022
One aspect of dictatorships that citizens of democratic nations often find puzzling is how the population can be convinced to support such dystopian policies. How do they get people to run those concentration camps? How do they find people to take food from starving villagers? How can they get so many people to support policies that, to any outsider, are so needlessly destructive, cruel, and dumb?
The answer lies in forced preference falsification. When those who speak up in principled opposition to a dictator’s policies are punished and forced into silence, those with similar opinions are forced into silence as well, or even forced to pretend they support policies in which they do not actually believe. Emboldened by this facade of unanimity, supporters of the regime’s policies, or even those who did not previously have strong opinions, become convinced that the regime’s policies are just and good—regardless of what those policies actually are—and that those critical of them are even more deserving of punishment.
One of history’s great masters of forced preference falsification was Chairman Mao Zedong. As László Ladány recalled, Mao’s decades-long campaign to remold the people of China in his own image began as soon as he took power after the Chinese Civil War.
By the fall of 1951, 80 percent of all Chinese had had to take part in mass accusation meetings, or to watch organized lynchings and public executions. These grim liturgies followed set patterns that once more were reminiscent of gangland practices: during these proceedings, rhetorical questions were addressed to the crowd, which, in turn, had to roar its approval in unison—the purpose of the exercise being to ensure collective participation in the murder of innocent victims; the latter were selected not on the basis of what they had done, but of who they were, or sometimes for no better reason than the need to meet the quota of capital executions which had been arbitrarily set beforehand by the Party authorities. From that time on, every two or three years, a new “campaign” would be launched, with its usual accompaniment of mass accusations, “struggle meetings,” self-accusations, and public executions… Remolding the minds, “brainwashing” as it is usually called, is a chief instrument of Chinese communism, and the technique goes as far back as the early consolidation of Mao’s rule in Yan’an.
This decades-long campaign of forced preference falsification reached its apex during the Cultural Revolution, in which Mao deputized radical youths across China, called Red Guards, to purge all vestiges of capitalism and traditional society and impose Mao Zedong Thought as China’s dominant ideology. Red Guards attacked anyone they perceived as Mao’s enemies, burned books, persecuted intellectuals, and engaged in the systematic destruction of their country’s own history, demolishing China’s relics en masse.
Through this method of forced preference falsification, any mass of people can be made to support virtually any policy, no matter how destructive or inimical to the interests of the people. Avoiding this spiral of preference falsification is therefore why freedom of speech is such a central tenet of the Enlightenment, and why it is given such primacy in the First Amendment of the US Constitution. No regime in American history has ever previously had the power to force preference falsification by systematically and clandestinely silencing those critical of its policies.
Until now. As it turns out, an astonishing new release of discovery documents in Missouri v. Biden—in which NCLA Legal is representing plaintiffs including Jay Bhattacharya, Martin Kulldorff, and Aaron Kheriaty against the Biden administration for violations of free speech during Covid—reveal a vast federal censorship army, with more than 50 federal officials across at least 11 federal agencies having secretly coordinated with social media companies to censor private speech.
Secretary Mayorkas of DHS commented that the federal Government’s efforts to police private speech on social media are occurring “across the federal enterprise.” It turns out that this statement is true, on a scale beyond what Plaintiffs could ever have anticipated. The limited discovery produced so far provides a tantalizing snapshot into a massive, sprawling federal “Censorship Enterprise,” which includes dozens of federal officials across at least eleven federal agencies and components identified so far, who communicate with social-media platforms about misinformation, disinformation, and the suppression of private speech on social media—all with the intent and effect of pressuring social-media platforms to censor and suppress private speech that federal officials disfavor.
The scale of this federal censorship enterprise appears to be far beyond what anyone imagined, involving even senior White House officials. The government is protecting Anthony Fauci and other high level officials by refusing to reveal documents related to their involvement.
The discovery provided so far demonstrates that this Censorship Enterprise is extremely broad, including officials in the White House, HHS, DHS, CISA, the CDC, NIAID, and the Office of the Surgeon General; and evidently other agencies as well, such as the Census Bureau, the FDA, the FBI, the State Department, the Treasury Department, and the U.S. Election Assistance Commission. And it rises to the highest levels of the U.S. Government, including numerous White House officials… In their initial response to interrogatories, Defendants initially identified forty-five federal officials at DHS, CISA, the CDC, NIAID, and the Office of the Surgeon General (all within only two federal agencies, DHS and HHS), who communicate with social-media platforms about misinformation and censorship.
Federal officials are coordinating to censor private speech across all major social media platforms.
The third-party social-media platforms, moreover, have revealed that more federal agencies are involved. Meta, for example, has disclosed that at least 32 federal officials—including senior officials at the FDA, the U.S. Election Assistance Commission, and the White House—have communicated with Meta about content moderation on its platforms, many of whom were not disclosed in response to Plaintiffs’ interrogatories to Defendants. YouTube disclosed eleven federal officials engaged in such communications, including officials at the Census Bureau and the White House, many of whom were also not disclosed by Defendants. Twitter disclosed nine federal officials, including senior officials at the State Department who were not previously disclosed by Defendants.
Federal officials are granted privileged status by social media companies for the purpose of censoring speech on their platforms, and officials hold weekly meetings on what to censor.
These federal bureaucrats are deeply embedded in a joint enterprise with social-media companies to procure the censorship of social-media speech. Officials at HHS routinely flag content for censorship, for example, by organizing weekly “Be On The Lookout” meetings to flag disfavored content, sending lengthy lists of examples of disfavored posts to be censored, serving as privileged “fact checkers” whom social-media platforms consult about censoring private speech, and receiving detailed reports from social-media companies about so-called “misinformation” and “disinformation” activities online, among others.
Social media companies have even set up secret, privileged channels to give federal officials expedited means to censor content on their platforms.
For example, Facebook trained CDC and Census Bureau officials on how to use a “Facebook misinfo reporting channel.” Twitter offered federal officials a privileged channel for flagging misinformation through a “Partner Support Portal.” YouTube has disclosed that it granted “trusted flagger” status to Census Bureau officials, which allows privileged and expedited consideration of their claims that content should be censored.
Many suspected that some coordination between social media companies and the federal government was occurring, but the breadth, depth, and coordination of this apparatus is far beyond what virtually anyone imagined. And the scale of this censorship apparatus raises troubling questions.
How could so many federal officials be convinced to engage in the clandestine censorship of opposition to tin-pot public health policies from China which have killed tens of thousands of young Americans and—let’s be honest—were never really that popular to begin with? The answer, I believe, is that high-level White House officials such as Anthony Fauci must have been simultaneously threatening social media companies if they did not comply with federal censorship demands, while also threatening entire federal bureaucracies if they did not toe the Party line.
By simultaneously threatening both the federal bureaucracy and social media companies, a handful of high-level officials could effectively transform the federal government into a sprawling censorship army reminiscent of Mao’s Red Guards, silencing any opposition to tin-pot public health policies with increasing detachment and certitude as this systematic silencing falsely convinced them that the regime’s policies were just and good. A few of these federal employees must have eventually let slip to the Republicans that this jawboning was taking place, which appears to have been how this suit began.
In plaintiff Aaron Kheriaty’s words:
Hyperbole and exaggeration have been common features on both sides of covid policy disputes. But I can say with all soberness and circumspection (and you, kind readers, will correct me if I am wrong here): this evidence suggests we are uncovering the most serious, coordinated, and large-scale violation of First Amendment free speech rights by the federal government’s executive branch in US history.
Michael P Senger is an attorney and author of Snake Oil: How Xi Jinping Shut Down the World.
Why the COVID Jab Should Be Banned for Pregnant Women
By Dr. Joseph Mercola | August 30, 2022
Since the rollout of the experimental COVID shots, U.S. health officials have adamantly claimed the shots are safe for pregnant women, and have been urging all pregnant women to get the jab “to protect themselves and their babies.” To this day, the U.S. Centers for Disease Control and Prevention recommends the COVID shot for:1
“… people who are pregnant, breastfeeding, trying to get pregnant now, or might become pregnant in the future.”
The CDC further recommends:2
“People who are pregnant should stay up to date with their COVID-19 vaccines, including getting a COVID-19 booster when it’s time to get one.”
And claims:3
“Evidence continues to build showing that:
- COVID-19 vaccination during pregnancy is safe and effective.
- There is currently no evidence that any vaccines, including COVID-19 vaccines, cause fertility problems in women or men.”
All the while, they’ve had Pfizer data showing the shots cause shocking rates of miscarriage which, adding insult to injury, have been blatantly miscategorized as a “recovered/resolved” adverse effect.4 Who in their right mind would consider DEATH a resolved side effect unless they had a depopulation agenda in mind all along?
I don’t see how this could be described as anything but a criminal cover-up. The only reason we know any of this is because U.S. District Judge Mark Pittman ordered the U.S. Food and Drug Administration to release Pfizer documents at a rate of 55,000 pages per month. The FDA and Pfizer had asked to release the documents at a pace of 500 pages per month, which meant it would take 75 years to disclose them all.5
Criminal Cover-Up
Dr. Naomi Wolf recently reported that an analysis of Pfizer data revealed 44% of the women in the trial suffered miscarriages.6 That statistic turns out to have been the result of a miscalculation,7 as Pfizer listed the miscarriages in two separate columns, resulting in them being counted twice.
We’ve repeatedly found Pfizer’s data collection and reporting to be all over the place, and seemingly on purpose, to make hazards more difficult to ascertain. Wolf admitted the error and took down the original report. However, while fact checkers are gloating over the perceived victory, there’s plenty of other evidence in the Pfizer material to demonstrate these shots should be banned for all time.
In an August 20, 2022, Substack article, Dr. Pierre Kory addressed other, “absolutely horrifying,” findings on miscarriages found in the Pfizer data dumps:8
“… let’s do a dive on just one page of the many thousands. See below, Section 5.3.6, Page 12 of the document called ‘Cumulative Analysis of Post-Authorization Adverse Event Reports.’
Looking at the first bullet under the header: Pregnancy cases: 274 cases including:
In this paragraph, at first read, it is just a list of adverse events and numbers, detailed in a way that is confusing at best, and obfuscating at worst. I think it is the latter because, if you do some simple arithmetic trying to parse that paragraph, you end up with this:
270 pregnancies were reported in vaccinated women during the first 12 weeks of the vaccine campaign. In 238 of them, ‘no outcome was provided.’ So, they only knew the outcome of 32 pregnancies reported. What happened in those 32 pregnancies they followed up on?
My hands are literally trembling as I write this, but here goes. In these 32 pregnancies, there were:
•23 spontaneous abortions
•2 spontaneous abortions with intra-uterine death
◦So, 25 of the 32 pregnancies with known outcomes resulted in a miscarriage, a rate of 78%. Note that miscarriage normally occurs in only 12-15% of pregnancies
•2 premature births with neonatal death
•1 spontaneous abortion with neonatal death
•1 normal outcome
Note that this only adds up to 29 known outcomes, but then they note that ‘two different outcomes were reported for each twin’ and then they talk about ‘fetus/baby cases as separate from mother cases.’ I have no idea how to interpret this explanation of outcomes, so it may have been one or two less (or more) deaths then.
So, of the 32 pregnancies they knew the outcome of, 87.5% resulted in the death of the fetus or neonate. Burying this data in the way and not alerting the world to what they found, is criminal activity …”
To be perfectly clear, the failure to record and report the outcomes of 238 out of 274 pregnancies during a drug trial is simply unheard of. It’s shockingly unethical. And the fact that both the Food and Drug Administration and the CDC accepted this, and claim there’s “no evidence” of harm to pregnant women and their babies is proof positive of reprehensible maleficence.
There’s no fixing what’s gone wrong at the FDA and CDC. Their credibility with the public is ruined beyond any possible recovery. The CDC can review and reorganize itself all it wants, but it changes nothing. They are, to this day, urging pregnant women to take a shot that they KNOW will cause babies to die. Calling it a dystopia of epic proportions is a profoundly serious understatement.
CDC-Sponsored Study Also Tried to Hide Data
Need more evidence? How about the fact that the CDC-sponsored study9 published in The New England Journal of Medicine (NEJM) in April 2021 — which was widely used to support the U.S. recommendation for pregnant women to get injected — also obfuscated data to hide a shockingly elevated miscarriage rate.
According to this paper, the miscarriage rate within the first 20 weeks of pregnancy was 12.5%, which is only slightly above the normal average of 10%. (Looking at statistical data, the risk of miscarriage drops from an overall, average risk rate of 21.3% for the duration of the pregnancy as a whole, to just 5% between Weeks 6 and 7, all the way down to 1% between Weeks 14 and 20.10)
However, there’s a distinct problem with this calculation, as highlighted by Drs. Ira Bernstein, Sanja Jovanovic and Deann McLeod, HBSc, of Toronto. In a May 28, 2021, letter to the editor, they pointed out that:11
“In table 4, the authors report a rate of spontaneous abortions <20 weeks (SA) of 12.5% (104 abortions/827 completed pregnancies). However, this rate should be based on the number of women who were at risk of an SA due to vaccine receipt and should exclude the 700 women who were vaccinated in their third-trimester (104/127 = 82%).”
In other words, when you exclude women who got the shot in their third trimester (since the third trimester is after week 20 and therefore should not be counted when determining miscarriage rate among those injected before week 20), the miscarriage rate is 82%. (The errors in that NEJM article were also reviewed in a Science, Public Health Policy and the Law paper12 published in November 2021.)
Of those 104 miscarriages, 96 of them occurred before 13 weeks of gestation, which strongly suggests that getting a COVID shot during the first trimester is an absolute recipe for disaster. So, here was yet another attempt to hide the fact that more than 8 in 10 pregnancies may be terminated as a result of the jab.
As of August 12, 2022, the U.S. Vaccine Adverse Event Reporting (VAERS) database listed 4,941 miscarriages post-COVID jab.13 For comparison, the fetal death reports for all other vaccines reported to VAERS in the last 30 years is 2,239.14
Birth Rates Are Suddenly Plummeting Worldwide
In addition to miscarriages, we’re also looking at abruptly plummeting birth rates, suggesting the COVID jabs are having an adverse impact on future fertility as well.
“They are large drops, and they are occurring, almost like clockwork, approximately 9 months after pregnant women around the world started to be vaccinated,” Kory notes.15
For example, Germany recently released data showing a 10% decline in birth rate during the first quarter of 2022.16
The live birth rate graph for Sweden looks much the same, with a 14% drop:17,18 According to Gunnar Anderson, a Swedish professor in demographics at Stockholm University, “We have never seen anything like this before, that the bottom just falls out in just one quarter.”19
Between January and April 2022, Switzerland’s birth rate was 15% lower than expected, the U.K.’s was down by 10% and Taiwan’s was down 23%.20,21,22 In Hungary, MP Dúró Dóra has expressed concern about a 20% drop in birth rate during January 2022, compared to January 2021.23
The U.S. is also showing signs of a drop in live births. Provisional data from North Dakota show a 10% decline in February 2022, 13% reduction in March and an 11% reduction in April, compared to the corresponding months in 2021.24
In a July 5, 2022, Counter Signal article, Mike Campbell reported that in the five countries with the highest COVID jab uptake, fertility has dropped by an average of 15.2%, whereas the five countries with the lowest COVID jab uptake have seen an average reduction of just 4.66%. Below is a chart from Birth Gauge25 on Twitter comparing live birth data for 2021 and 2022 in a large number of countries.
Many Women Report Menstrual Irregularities Post-Jab
High rates of menstrual irregularities post-jab are also a warning sign that reproductive capacity may be impacted. As of August 12, 2022, there were 31,443 VAERS reports of menstrual disorders.26
Changes include heavier and more painful periods27 and changes in menses length, as well as unexpected breakthrough bleeding or spotting among women on long-acting contraception or those who are postmenopausal and haven’t had a period in years or even decades.28
Health officials have tried to brush off the reports, but a study published in Obstetrics & Gynecology — funded by the National Institute of Child Health and Human Development (NICHD) and the National Institutes of Health’s Office of Research on Women’s Health — confirmed an association between menstrual cycle length and COVID-19 shots.29
According to the authors, it’s possible that the immune response created by the mRNA shots affect the hypothalamic-pituitary-ovarian axis, which plays a well-known role in the timing of a woman’s cycle:30
“Our findings for individuals who received two doses in a single cycle supports this hypothesis. Given the dosing schedule of the mRNA COVID-19 vaccines in the United States (21 days for Pfizer and 28 days for Moderna), an individual receiving two doses in a single cycle would have received the first dose in the early follicular phase.
Cycle length variability results from events leading to the recruitment and maturation of the dominant follicle during the follicular phase …”
Other Disturbing Evidence
A Japanese biodistribution study for Pfizer’s jab also showed the COVID spike protein from the shots accumulate in female ovaries and male testes,31,32 and there’s credible concern that the COVID jabs will cross-react with syncytin (a retroviral envelope protein) and reproductive genes in sperm, ova and placenta in ways that may impair fertility and reproductive outcomes.
A Pfizer-BioNTech rat study33 revealed the injection more than doubled the incidence of preimplantation loss (i.e., the risk of infertility), and led to mouth/jaw malformations, gastroschisis (a birth defect of the abdominal wall) and abnormalities in the right-sided aortic arch and cervical vertebrae.34,35 As noted by The Exposé :
“With this being the case, how on earth have medicine regulators around the world managed to state in their official guidance that ‘Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy’? And how have they managed to state ‘It is unknown whether the Pfizer vaccine has an impact on fertility’?
The truth of the matter is that they actively chose to cover it up. We know this thanks to a Freedom of Information (FOI) request36 made to the Australian Government Department of Health Therapeutic Goods Administration (TGA).”
You can read more about that in The Exposé’s July 19, 2022, article, “FOIA Reveals Pfizer & Medicine Regulators Hid Dangers of COVID Vaccination During Pregnancy After Study Found It Increases Risk of Birth Defects & Infertility.”37
We’re also seeing a sudden uptick in infant mortality. The Exposé 38 highlighted data from Scotland, showing neonatal deaths were 119% higher above the annual norm in March 2022.
COVID Jab Affects Male Fertility Too
Male fertility is also under attack by these bioweapons. Israeli research39,40 published in the journal Andrology found the Pfizer COVID jab temporarily but significantly impairs male fertility, dropping sperm concentration by 15.4% and total motile count by 22.1%, compared to baseline pre-jab.
Both eventually recovered, some three months after the last jab, but if you destroy a man’s sperm for three months every time he gets a COVID shot, you’re significantly reducing the probability of him fathering a child for a good part of any given year and the stats reviewed above support this.
Remember, the mRNA shots are recommended at three-month intervals for the original series, and boosters are now being recommended at varying intervals thereafter. In the video above, Amy Kelly, project director for the Daily Clout’s Pfizer document analysis team, reviews this study and other post-jab male fertility concerns.41
End the COVID Shots Now, Before It’s Too Late to Recover
In October 2021, when the FDA was voting on whether to authorize the COVID jab for children aged 5 through 11, Dr. Eric Rubin, an FDA advisory panel member, Harvard professor and editor-in-chief of the NEJM, stated:42
“We’re never going to learn about how safe this vaccine is unless we start giving it. That’s just the way it goes … And I do think we should vote to approve it.”
So, in this and other instances, they’ve openly admitted that anyone who takes the jab is part of an experiment. Yet at the same time, the FDA and CDC have insisted that the jabs are perfectly safe — all while in possession of data showing they’re anything but! In conclusion, I agree with Kory, who writes:43
“… when a new medicine or device is introduced, you must first assume any adverse effects or deaths reported to be related to the intervention until proven otherwise. That is what I am doing here.
We must assume the vaccines are impacting fertility unless some other provable or credible explanations for a sudden drop in month to month birth rates. So stop the shots until you can prove they are not …
Too many young people dying,44 too many becoming disabled, too many pregnancies resulting in fetal or neonatal death as above, and now we find out that if we continue with this vaccine obsession, they will not be replaced. This is a humanitarian catastrophe heaped atop the one caused by dangerous gain-of-function research.
When will the world wake up to this rapidly unfolding horror? For those of us who know what is going on, it is hard not to feel helpless as we are forced to watch increasingly apparent and widespread needless death. But we will continue to try to get these truths out despite the massive censorship and propaganda overwhelming the globe.
We have a moral and ethical obligation and take that responsibility seriously no matter what befalls us. Stop the vaccines, now. And if we can’t stop them, we must try to convince everyone we know to no longer agree to get vaccinated. Their lives and our future depend on it.”
Sources and References
- 1, 2, 3 CDC.gov Updated July 14, 2022
- 4, 6 Clark County Today August 18, 2022
- 5 Bloomberg Law January 18, 2022
- 7 Twitter Phil Kerpen August 17, 2022
- 8, 15, 19, 43 Pierre Kory Substack August 20, 2022
- 9 N Engl J Med 2021; 384:2273-2282
- 10 Medical News Today January 12, 2020
- 11 Wayback NEJM Letter to the Editor June 27, 2021
- 12 Science, Public Health Policy, and the Law November 2021; 4: 130-143
- 13, 26 OpenVAERS Reproductive Health Reports as of August 12, 2022
- 14, 35, 38, 44 The Expose August 7, 2022
- 16 Expose News July 18, 2022
- 17, 20, 23 The Counter Signal July 5, 2022
- 18 Twitter Havard Skjaervik June 27, 2022
- 21, 24 Igor Chudov Substack June 25, 2022
- 22 SWPRS June 2022
- 25 Twitter Birth Gauge June 3, 2022
- 27 Boston University September 9, 2021
- 28 NPR August 9, 2021
- 29 Obstetrics & Gynecology: January 5, 2022 – Volume – Issue – 10.1097
- 30 Obstetrics & Gynecology: January 5, 2022 – Volume – Issue – 10.1097, Discussion
- 31 Children’s Health Defense June 3, 2021
- 32 Rights and Freedoms, Confidential Pfizer Research Document
- 33 Reproductive Toxicology August 2021; 103: 28-35
- 34 Science, Public Health Policy, and the Law November 2021; 4:130-143, page 135
- 36, 37 The Expose July 19, 2022
- 39 Andrology June 17, 2022 DOI: 10.111/andr.13209
- 40 Expose June 26, 2022
- 41 Daily Clout August 16, 2022
- 42 Townhall October 26, 2021
If It’s Okay for Mice, It’s Good Enough for People, Right?
By Madhava Setty, M.D. | The Defender | August 26, 2022
Its audacity on full display, Pfizer — arguably the most criminal corporation in history — has asked the U.S. Food and Drug Administration (FDA) to greenlight its new bivalent COVID-19 vaccine that targets the Omicron BA.4 and BA.5 subvariants for people 12 and older “to help the country prepare for potential fall and winter surges of the coronavirus,” Pfizer CEO Albert Bourla said in a statement.
Bourla’s good intentions are sadly thwarted by FDA regulations that require an Investigational New Drug (IND) application be submitted and approved before a drug can be tested in humans.
Luckily, the FDA can circumvent the inconvenience of its own regulatory processes by allowing itself the ability “to authorize use of an experimental drug in an emergency situation that does not allow time for submission of an IND in accordance with 21CFR, Sec. 312.23 or Sec. 312.20.”
Section 312.20 of the Code of Federal Regulations specifies that a clinical investigation cannot commence until an IND application has been submitted and approved. Nevertheless, Pfizer on Monday submitted an IND for its new formulation.
Now that the FDA and Pfizer have crossed their Ts and dotted their Is to make sure all the rules are followed, how do we know these products are safe and will work?
This is where the rodents come in — the products seem to work on mice.
As NPR reported, “For the first time, the FDA is planning to base its decision about whether to authorize new boosters on studies involving mice instead of humans.”
Yes, it’s an unprecedented move by the FDA, but Dr. Ofer Levy, professor of pediatrics at Harvard and advisor to the FDA argues that the country has had enough experience with the vaccines at this point to be confident the shots are safe and that there’s not enough time to wait for data from human studies.
He has a point. There were still only 30,479 uninvestigated deaths reported in VAERS after administration of the shots as of Aug. 19.
In any case, why should the FDA be concerned with such things as human studies in the first place?
This maneuver by the FDA may finally unshackle the agency from its overly restrictive responsibility to fulfill its own mission and become more agile in bringing products to market.
Not to be left behind, Moderna also requested the FDA authorize its bivalent vaccine for human beings over the age of 17.
Similar to the Pfizer vaccine, Moderna’s vaccine also, for good measure, will encode for the spike protein for the original ancestral SARS-CoV-2 strain, which for all intents and purposes, does not exist on our planet any longer.
Meryl Nass, M.D., summarized it this way:
“No clinical trials. (You need to obtain an IND before you can start testing the vaccine in humans. Pfizer applied 4 days ago.)”
Taking no chances, the FDA will not convene the Vaccines and Related Biological Products Advisory Committee (just like the first time the FDA authorized boosters) and has announced this today to see how much opposition the agency gets.
Can we dispense with the pretense any of this is about health?
No sane person vaccinates the entire country with an experimental vaccine without trials — particularly since the whole country already has some immunity, the virulence is low and the evidence supports higher all-cause mortality with an increasing number of vaccine doses.
What is in the vaccine that they are desperate to inject us with?
Madhava Setty, M.D. is senior science editor for The Defender.
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
Here’s what government and industry came up with to wiggle out of liability for monkeypox vaccine injuries
By Meryl Nass, MD | August 7, 2022
Although I don’t have the full story yet, I am warning you that the moneypox vaccine Jynneos is a huge scam, in every way, including the supposed shortage. I will disclose more about that soon.
But since it is actually licensed, the moneypox vaccine (like other licensed drugs and vaccines) has liability attached to it. You can currently sue government program planners, the doctor who recommended it, the manufacturer, etc. if anything goes wrong.
To forestall that, some crook came up with the idea of splitting the doses, under the guise of a fake shortage, which provides an excuse to make the lower dose an EUA–in other words, turning it into a product for which you cannot sue anyone if something goes wrong. Pretty clever, eh?
Licensed products are not supposed to receive EUAs unless they are used for something different than what they were licensed for. Splitting the dose does not change the fact it is licensed for monkeypox and being used for moneypox.
Here is another possible but diabolical reason to split (dilute) the dose: it potentially allows the federal government access to the vials–so the vials won’t go straight from the manufacturer to the wholesaler but instead go somewhere else to be diluted. And what is in the diluent?
From the NY Times :
… Federal officials have ordered nearly seven million doses of Jynneos, but the shots will not arrive for months. So far, the Biden administration has shipped about 600,000 doses to states. It said last week that 800,000 additional doses were being allocated to states, but the distribution could take weeks.
Faced with shortages, some cities, including Washington and New York, are restricting second doses to stretch their supplies. Officials at the Food and Drug Administration and the C.D.C. have disagreed with that strategy, noting that Jynneos is approved as a vaccine to be given in two doses spaced 28 days apart.
But as federal health officials declared a public health emergency on Thursday, Dr. Robert Califf, the commissioner of the F.D.A., said the agency was now considering authorizing shots that contain just one-fifth of the regular dose, delivered between layers of the skin instead of under it.
The F.D.A. would need to grant Jynneos an emergency use authorization in order for it to be administered this way.
The dose-sparing approach has been used when supplies of other vaccines are scarce. But giving intradermal shots requires more skill than is needed for more traditional immunizations.
One shot is probably enough to forestall severe symptoms in most people, and the dose-sparing strategy may work just as well. But it’s unclear whether a scaled-back regimen is enough to prevent infection, and if so, how long that immunity may last, federal health officials said…
U.S. Declares Monkeypox Health Emergency, FDA Offers Vaccine to Some Kids Despite No Clinical Trials
By Megan Redshaw | The Defender | August 5, 2022
The U.S. declared monkeypox a public health emergency to raise awareness and allow for additional funding to fight the disease’s spread, U.S. Department of Health and Human Services Secretary Xavier Becerra said on Thursday.
“We’re prepared to take our response to the next level in addressing this virus, and we urge every American to take monkeypox seriously and to take responsibility to help us tackle this virus,” Becerra said.
Becerra said he also is considering a second declaration that would allow federal officials to expedite medical countermeasures — such as potential treatments and vaccines — designed to ensure drugs are safe and effective.
President Biden said in a tweet he remained “committed to our monkeypox response: ramping-up vaccine distribution, expanding testing, and educating at-risk communities.”
“That’s why today’s public health emergency declaration on the virus is critical to confronting this outbreak with the urgency it warrants,” Biden said.
The last time the U.S. declared a public health emergency was in January 2020, for COVID-19.
According to the Centers for Disease Control and Prevention (CDC), more than 7,100 cases of monkeypox have been reported in the U.S., including five cases in children.
Symptoms of monkeypox infection are usually mild and include fever, rash and swollen lymph nodes, and occasionally intense headache, back pain, muscle aches, lack of energy and skin eruptions that can cause painful lesions, scabs or crusts.
The virus is rarely fatal and no deaths have been reported in the U.S.
Monkeypox primarily is spread through skin-to-skin contact during sex and affects mostly gay and bisexual men, public health officials say, although the virus can affect anyone.
According to the CDC, about 98% of monkeypox patients who provided demographic information to clinics identified as men who have sex with men.
Public health emergency paves way for vaccine for kids
Now that the Biden administration has declared the monkeypox outbreak a public health emergency, the U.S. Food and Drug Administration (FDA) can move to issue an Emergency Use Authorization for the JYNNEOS vaccine for children under 18.
There are two vaccines that may be used “for the prevention” of monkeypox virus infection: JYNNEOS — also known as Imvamune or Imvanex — and ACAM2000, which is licensed by the FDA for use against smallpox and “made available for use against monkeypox under an Expanded Access Investigational New Drug application.”
The FDA told ABC News on Thursday that while the current monkeypox vaccine, JYNNEOS, is approved only for adults ages 18 and older, it will be available for kids on a case-by-case basis.
The JYNNEOS vaccine, delivered in a two-dose series, was not tested through clinical trials in children.
However, the FDA confirmed to ABC News that “numerous” children have been granted access to the vaccine through a special permission process, but declined to state exactly how many children have received the vaccine to date through this process.
“If a doctor decides a person under 18 was exposed to monkeypox and the benefit of the vaccine is greater than any potential risk, they can submit a request to the FDA,” ABC News reported.
According to the CDC, the “immune response” takes “14 days after the second dose of JYNNEOS and 4 weeks after the ACAM2000 dose for maximal development.”
The CDC website also states: “No data are available yet on the effectiveness of these vaccines in the current outbreak.”
According to the latest data from the Vaccine Adverse Event Reporting System (VAERS), between June 14 and July 21, 2022, 31 adverse events were reported following vaccination with JYNNEOS — manufactured by Bavarian Nordic.
The World Health Organization (WHO) declared monkeypox a global health emergency after more than 26,000 cases were reported across 87 countries.
A global emergency is the WHO’s highest level of alert, but the designation does not necessarily mean a disease is particularly transmissible or lethal.
The U.S. makes up 25% of confirmed cases globally although the U.K. was the first to alert the world to the outbreak in May after confirming several cases.
A monkeypox fictional simulation was held in March 2021
As The Defender reported in May, the Nuclear Threat Initiative, in conjunction with the Munich Security Conference, in March 2021 held a “tabletop exercise on reducing high-consequence biological threats,” involving an “unusual strain of monkeypox virus that first emerged in the fictional nation of Brinia and spread globally over 18 months.”
This is similar to “Event 201,” a “high-level pandemic exercise” organized by the Johns Hopkins Center for Health Security, along with the World Economic Forum and the Bill & Melinda Gates Foundation — just weeks before the COVID-19 outbreak — that mirrored what later followed with COVID-19 pandemic.
According to the Nuclear Threat Initiative, the monkeypox exercise, which was “developed in consultation with technical and policy experts,” brought together “19 senior leaders and experts from across Africa, the Americas, Asia, and Europe with decades of combined experience in public health, biotechnology industry, international security, and philanthropy.”
The fictional start date of the monkeypox pandemic in this exercise was May 15, 2022. The first European case of monkeypox was identified on May 7, 2022.
Key participants in the simulation included Johnson & Johnson and Janssen, the Bill & Melinda Gates Foundation, the Chinese Centers for Disease Control and Prevention, the Nuclear Threat Initiative, GAVI — the Vaccine Alliance, Merck and the WHO.
Several of the participants listed above also “participated” in Event 201.
Megan Redshaw is a staff attorney for Children’s Health Defense and a reporter for The Defender.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
New Evidence: Fauci Imposed a Vaccine Delay that Cost Trump the Election
By Toby Rogers | July 31, 2022
I. Fauci fires Trump
Think back to July 2020. Trump and Fauci were at war with each other. Key leaders within the Trump administration, including Peter Navarro, wanted to fire Fauci. There were riots in the streets as people protested the murder of George Floyd. And new evidence shows that behind the scenes, Fauci was working to torpedo Trump’s chances for re-election.
We already knew that Fauci, the FDA, CDC, and the pharmaceutical industry went to great lengths to block safe and effective treatments including hydroxychloroquine and ivermectin in order to prolong the pandemic and create the market for Covid-19 vaccines. But a new book reveals that Fauci also forced Moderna to delay their clinical trial by three weeks — which pushed the release of their preliminary results until after the presidential election.
This key piece of information comes from The Messenger: Moderna, the Vaccine, and the Business Gamble That Changed the World published last week by Harvard Business Review Press. The author, Peter Loftus, is a reporter for the Wall Street Journal and they published his essay about the book in their Review section on Saturday. What’s astonishing is that Loftus does not even realize the enormity of the story he just stumbled upon. Cultural capture and too many shots apparently prevent one from connecting the dots, so I will do it for him.
Most people already know the broad brush strokes of the Moderna story — they had never successfully brought a product to market before Operation Warp Speed. They were grifters — they took $25 million from the Defense Advanced Research Projects Agency (DARPA) in 2013 to develop mRNA products that never worked and another $125 million from the Biomedical Advanced Research and Development Authority (BARDA) in 2015 for a vaccine for Zika that also failed. But Fauci really liked these grifters and so when the pandemic began in 2020, BARDA directed $483 million to Moderna for Covid-19 vaccine development — and Moderna cut NIH in on the patents. That gave NIH and especially Fauci control over what came next.
The key paragraphs from Loftus’ WSJ essay are here:
Dr. Zaks [Chief Medical Officer for Moderna] had wanted to use a private contract research organization to run the whole trial, but NIAID officials wanted their clinical-trial network involved. Eventually, Dr. Zaks backed off, and both entities participated. “I realized we were at an impasse, and I was the embodiment of the impasse,” Dr. Zaks said.
Next, when Moderna’s 30,000-person study began enrolling volunteers in July 2020, the subjects weren’t racially diverse enough. Moncef Slaoui, who led Warp Speed’s vaccine efforts, and Dr. Fauci began holding Saturday Zoom calls with Mr. Bancel and other Moderna leaders to “help coax and advise Moderna how to get the percentage of minorities up to a reasonable level,” Dr. Fauci recalled.
Drs. Fauci and Slaoui wanted Moderna to slow down overall enrollment, to give time to find more people of color. Moderna executives resisted at first. “That was very tense,” Dr. Slaoui said. “Voices went up, and emotions were very high.” Moderna ultimately agreed, and the effort worked, but it cost the trial about an extra three weeks. Later, Mr. Bancel called the decision to slow enrollment “one of the hardest decisions I made this year.”
The claim that Fauci cared about racial diversity in the clinical trial is a lie. How do we know this? Later “clinical trials” for Pfizer and Moderna in kids looked at antibodies in the blood, not actual health outcomes, in only about 300 study participants. The number of people of color enrolled in those undersized trials were in the single digits (literally two or three Black participants total) — so those results were not statistically significant. Yet this did not stop authorization. It appears that Fauci’s delay tactics were designed to accomplish a different goal.
Let’s do the math:
Moderna released their preliminary results — claiming 94.5% effectiveness — on November 16, 2020.
The presidential election was less than two weeks earlier — on November 3, 2020.
Trump lost by less than 1% of the vote in 4 key swing states.
Fauci’s demand to slow down enrollment in July 2020 cost Moderna 3 weeks.
If Moderna had released their results 3 weeks earlier — on October 25, 2020, Trump would have scored a major win in the final week of the campaign and won the election.
It does not matter how one feels about Trump or Biden. A massive political win in the week before the election would have convinced enough voters of Trump’s competence and thus pushed Trump’s vote total over the top.
What about Pfizer? They also could have published their preliminary results prior to the election which would have secured Trump’s re-election. According to Loftus, Pfizer “opted out of Operation Warp Speed for fear it would slow the company down.” Pfizer still took $2 billion off of the Trump administration for advance purchase orders. But Scott Gottlieb and Pfizer clearly preferred Biden and so they held their preliminary results until November 9, 2020 — just 6 days after the election. The Biden administration returned the favor by giving Pfizer a blank check and authorizing shots for additional age groups based on the worst “clinical trial” results anyone has ever seen.
The important thing to understand in all of this is that Fauci, the FDA, NIH, and CDC are political functionaries pretending to be scientists. Pandemics, vaccines, and public health are a way for the Democratic Party machine to direct billions of dollars to their base and reward large donors to the party. These companies and their bureaucratic enablers were happy to take money off of Trump. But they knew that they could get an even better deal from Biden.
As you know, the results of this criminal scheme are gruesome. The Covid-19 shots authorized right after the 2020 election have made no discernible impact on the course of the pandemic. Far more people have died of Covid-19 since the introduction of the shots under Biden than during the Trump administration when no Covid-19 shots existed. The Covid-19 shots have negative efficacy and even quadruple-dosed Biden and quadruple-dosed Fauci have contracted Covid-19, twice. These are the deadliest and most toxic shots in the history of the world.
So what started out as a grift turned into mass murder and a crime against humanity.
And now it’s happening again…
II. Pfizer and Moderna move up the release date for reformulated Covid-19 shots in the effort to help Democrats win the midterm elections
On Thursday of last week, the White House and the FDA told their favorite stenographers at the NY Times that Moderna and Pfizer are going to release their reformulated Covid-19 shots, that will completely skip clinical trials, in mid-September.
As readers of my Substack will recall, back on June 28, Pfizer said that the fastest the reformulated shots could be released was October; Moderna said “late October or November” — provided they could skip clinical trials (which of course the FDA granted because they work for Pharma). Did Pfizer and Moderna not understand their own production capabilities? How did Pfizer and Moderna suddenly speed up their production schedule by 6 weeks?
It appears that once again, the public health gatekeepers are doing politics not science. If shots go into bodies in the last two weeks of September, Democrats will claim progress against Covid during October right before the midterm elections on November 8. It’s basically the political win that these same actors denied to Trump (it’s not a public health win, as I will show below).
What’s likely driving this is that Fauci, Pfizer, Moderna, the FDA, CDC, and NIH all want Democrats to retain the House and Senate in order to prevent hearings into their bungling of the Covid-19 response. Of course they also want to keep the Covid-19 vaccine gravy train going as long as possible.
But, you’re surely saying to yourself, we know that these 5th dose reformulated shots are likely to cause catastrophic harms. We’re already seeing a 5% to 15% increase in all-cause mortality across the most heavily vaccinated countries as a result of non-specific effects from these shots. There are 29,790 VAERS reports of death following these shots and this is likely an underestimate by a factor of 41 (so actual death toll = 1,221,390). These reformulated shots are going to use a form of mRNA never tried before and skip clinical trials altogether, so the harms could be even worse. There also seem to be cumulative harms from these shots — the more doses, the more messed up the immune system, the more vulnerable one is to Covid and all sorts of other diseases including cancer.
So how exactly do they plan to get away with this, especially right before an election?
The same way they always get away with it — they own the media. Pfizer and Moderna will rush out press releases claiming that these reformulated shots are a miracle. The CDC’s in-house newsletter, MMWR, will rush out articles and janky studies claiming that these reformulated shots are a miracle. The mainstream media will dutifully report that these reformulated shots are a miracle. Meanwhile, people you know and love — coworkers, friends, neighbors, and family — will be getting injured and killed by these shots. Yet all of the stories in the news will be hosannas about the genius of Tony Fauci, Peter Marks, and the FDA. Billions of dollars of dark money from Pharma will flow into Democratic Congressional campaign coffers. If Democrats can retain the House and Senate they will reward Pfizer and Moderna by blocking any inquiry into the failed Covid-19 response. Win, win, win for Pharma. Everyone else loses.
Which brings me to my last point….
III. Republicans, you have to step up and fight for us or you will lose
Republicans thought that they could take back the House and Senate simply by not being Democrats. Most Republicans did not really fight for us, they just sat back and let Dems destroy themselves. That plan was working until the Supreme Court overturned Roe. Now the Republican advantage in the generic Congressional ballot (‘which party do you prefer’) has evaporated. Pelosi has passed a range of popular bills. Manchin has fallen in line so Biden will likely get some late legislative wins. Gas prices have declined somewhat. And now it appears that Democrats, who were left for dead just weeks ago, will retain the Senate and may retain the House.
IF REPUBLICANS WANT TO WIN THE MIDTERM ELECTIONS THEY HAVE TO MAKE IT ABOUT DEMOCRATS’ FAILED RESPONSE TO COVID!
No more sitting back. No more making warrior mamas do all of the emotional labor for our country. If Republicans want to win they have to make it clear that they will fire, arrest, and prosecute Fauci (and all of his lieutenants) as soon at Republicans take power. Fauci funded the creation of the chimera virus, blocked access to safe and effective treatments, and inflicted deadly toxic vaccines on the entire population. Over 2 million Americans are dead as a direct result of Fauci’s corruption (1 million dead from/with Covid, over 1 million dead from the shots). If Republicans cannot be bothered to sink this two-foot putt then they don’t deserve to win. If Republicans want the votes of the 18 million single-issue medical freedom voters who decide every national election these days — that’s what they have to run on: #ArrestFauci!
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Chris Matthews got it: Neocons want to destroy the Middle East for Israel
By Jonas E. Alexis | Veterans Today | August 4, 2107
Chris Matthews attacked the Neocon project in 2015 by saying that the Neocons and warmongers in the United States aspire to create complete chaos in the Middle East, presumably for Israel. His words are worth quoting in full:
“Why were the people in the administration like [Paul] Wolfowitz and the others talking about going into Iraq from the very beginning, when they got into the white house long before there was a 911 long before there was WMD. It seemed like there was a deeper reason. I don’t get it. It seemed like WMD was a cover story.
“The reason I go back to that is there’s a consistent pattern: the people who wanted that war in the worst ways, neocons so called, Wolfowitz, certainly Cheney.. it’s the same crowd of people that want us to overthrow Bashar Assad, .. it’s the same group of people that don’t want to negotiate at all with the Iranians, don’t want any kind of rapprochement with the Iranians, they want to fight that war. They’re willing to go in there and bomb.
“They have a consistent impulsive desire to make war on Arab and Islamic states in a never-ending campaign, almost like an Orwellian campaign they will never outlive, that’s why I have a problem with that thinking. … we’ve got to get to the bottom of it. Why did they take us to Iraq, because that’s the same reason they want to take us into Damascus and why they want to have permanent war with Iran.”
Yours truly and many others have been saying the same thing for years. We would not have perpetual wars in the Middle East if the Neocons did not take their orders from Israel. Even George W. Bush implicitly admitted this.
George W. Bush once asked his father to define Neoconservatism. “‘What’s a neocon?’ ‘Do you want names, or a description?’ answered [the elder Bush]. ‘Description.’ ‘Well,’ said the former president of the United States, ‘I’ll give it to you in one word: Israel.’”[1] … continue
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