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COVID-19

Lawsuit accuses CIA of withholding possible evidence that its analysts took bribes to conceal lab origin of COVID-19

A new federal lawsuit accuses the CIA of withholding possible evidence that its analysts were paid to deep-six findings that the most likely cause of the COVID-19 pandemic was a Chinese lab leak.

The lawsuit, filed Friday by the Heritage Foundation’s Oversight Project and obtained by the Daily Caller, suggests that just as the CIA has neglected to publicly provide congressional investigators with the information they requested, it has similarly failed to provide Heritage with a timely response.

What’s the background?

A CIA whistleblower described as a “multi-decade, senior-level” official claimed in September that the agency bribed six analysts on its COVID Discovery Team to reject the theory that the COVID-19 virus initially spread as the result of a research-related leak at China’s Wuhan Institute of Virology — a communist-controlled lab controversial for its dangerous experiments on coronviruses.

Blaze News previously noted that federal documents obtained through a Freedom of Information Act lawsuit revealed earlier this year that the National Institute of Allergy and Infections Diseases, under former director Anthony Fauci, funded experiments at the WIV.

Millions among the dollars funneled from Fauci’s agency to the WIV were mediated by Peter Daszak’s EcoHealth Alliance, whose subcontractor Ben Hu — the lead on gain-of-function research on SARS-like coronaviruses — was among the patients zero at the lab and ostensibly among the very first infected in the world.

According to a Sept. 12 letter penned by House Intelligence Committee Chairman Mike Turner (R-Ohio) and Select Subcommittee on the Coronavirus Pandemic Chairman Brad Wenstrup (R-Ohio), the CIA whistleblower revealed that at the end of its review, six of the seven members of the COVID Discovery Team “believed the intelligence and science were sufficient to make a low confidence assessment that COVID-19 originated from a laboratory in Wuhan, China. The seventh member of the Team, who also happened to be the most senior, was the lone officer to believe COVID-19 originated through zoonosis.”

The whistleblower indicated that “to come to the eventual public determination of uncertainty, the other six members were given a significant monetary incentive to change their position.”

The whistleblower’s allegations were significant because a declassified report released in June by the director of national intelligence stated, “The Central Intelligence Agency and another agency remain unable to determine the precise origin of the COVID-19 pandemic, as both hypotheses rely on significant assumptions or face challenges with conflicting reporting.”

In response to the whistleblower testimony, congressional lawmakers demanded that the CIA turn over all documents and communications pertaining to the COVID Discovery Team, its establishment, and its investigation of the origins of the virus, as well as all documents pertaining to members’ pay history, by no later than Sept. 26.

Republican senators similarly wrote to CIA Director William Burns in early September demanding transparency on this issue.

The Heritage Foundation and Mike Howell of the Oversight Project then hit the agency with a Freedom of Information Act request to the same effect on Sept. 20.

The FOIA suit

Heritage indicated in its Friday complaint that the CIA did not ultimately comply with its September FOIA request regarding who allegedly “received monetary incentives to change their position on the origins of the virus.”

The complaint asked the U.S. District Court for the District of Columbia to compel the CIA to both “conduct a search or searches reasonably calculated to uncover all records responsive to Plaintiffs’ FOIA Request” and to produce all non-exempt records inside 20 days of the court’s order or “by such other date as the Court deems appropriate.”

“The Biden administration has refused to be transparent with Congress and the American people over the origins of COVID-19,” Kyle Brosnan, chief counsel for the Oversight Project, told the New York Post.

“A CIA whistleblower has made serious allegations that the agency bought off employees of the agency to further obstruct efforts to get to the truth of the virus’s origins,” continued Brosnan. “This obstruction cannot stand, and we’re fighting in federal court to get to the bottom of this.”

Fauci on the hot seat in 2024

It’s not just America’s spies whose feet are now being held to the fire.

Anthony Fauci, the former head of the National Institute of Allergy and Infectious Diseases, is set to testify before the Select Subcommittee on the Coronavirus Pandemic on Jan. 8 and Jan. 9.

The subcommittee noted on X that “thankfully, Dr. Fauci’s retirement from public service does not shield him from Congressional oversight nor accountability to the American people.”

The subcommittee further reminded the public that Fauci commissioned, edited, and gave final approval to the impactful March 2020 study published in the journal Nature, “The Proximal Origins of SARS-CoV-2” — an oft-cited study whose authors expressed concerns in private about the “sh** show that would happen if anyone serious accused the Chinese of even accidental release,” making clear that their cause was “political.”

Fauci repeatedly referenced this paper on the national stage, including once from the White House podium, to bolster the zoonotic origins theory ultimately entertained by the CIA team.

The subcommittee also highlighted how Fauci was cognizant of the dangerous gain-of-function research taking place in Wuhan but “did nothing to stop it or warn the American people.”

The subcommittee failed to mention in its short list of Fauci’s faux pas Wenstrup’s late-September revelation that “according to information gathered by the Select Subcommittee, Dr. Anthony Fauci, then-director of National Institute of Allergy and Infectious Diseases, played a role in the Central Intelligence Agency’s review of the origins of COVID-19.”

“The information provided suggests that Dr. Fauci was escorted into Central Intelligence Agency (CIA) Headquarters — without a record of entry — and participated in the analysis to ‘influence’ the Agency’s review,” continued the chairman.

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COVID-19

Congress should treat Pfizer’s RSV shot like a chemical abortion

With the public’s appetite for Pfizer’s COVID shot lower than ever and Pfizer’s stock price in the toilet, the pharmaceutical giant is relying on new mothers to take its next poison: The respiratory syncytial virus shot. The White House recently made hundreds of thousands of doses available to unsuspecting doctors who are completely ignorant about the history of this shot.

What if I told you Pfizer’s own clinical trial data shows its new RSV shot for pregnant women will cause death for thousands of babies?

In a sane world, the shots would never have been approved. But we are living in a “Twilight Zone” of “Warp Speed,” where nothing can slow down anything stamped with the “vaccine” label. If thousands of studies and data points proving the COVID shots deadly and dangerous did not slow down their speed, then nothing about any new shots will convince the warped minds of the biomedical security state to slow things down.

As members of Congress continue to fund the FDA, CDC, and National Institutes of Health this fiscal year without any reforms to vaccine approval and recommendation processes, nearly all of them are unaware of the fact that Pfizer’s new RSV shot is so problematic that its twin sister was aborted before application for approval.

British drug maker GlaxoSmithKline was the first out of the gate with an RSV shot for pregnant women decades after other companies had abandoned their research. But the prolific vaccine developer abruptly suspended the phase 3 clinical trial after observing multiple safety signals.

GSK abandoned the project completely in 2022 after somebody died. The death was attributed to “acute disseminated encephalomyelitis 22 days after vaccination,” which the drug maker and the FDA concluded could be related to the vaccine. The trial investigators also found a 6.8% rate of preterm births in the trial group compared to 4.9% in the placebo group. The rate of neonatal deaths was also double that of the placebo group.

The entire premise of vaccinating pregnant women is to pass along immunity to babies, a venture that has failed for a half-century since RSV shots were first terminated in the 1960s. Back then, the shots made babies sicker. Now we see a sharp increase in preterm births correlated with the vaccine.

Given the woefully low standards nowadays for ending vaccination programs, it had to be pretty bad for GSK to concede defeat.

Ordinarily, that would have been the end of the story. But since we now live in a country “brought to you by Pfizer,” the nightmare continues. Pfizer in August received full FDA approval for a nearly identical formulation of the shot. The shot is so similar, in fact, that GSK is suing Pfizer in U.S. federal court for patent infringement.

And yet, despite the deadly and unmistakable safety signals with GSK’s vaccine, Pfizer’s knockoff version, Abrysvo, sailed through the CDC and FDA approval process.

Nearly every OB-GYN is pressuring patients to get the shot, despite their complete ignorance about its potential risks. In September, the American College of Gynecologists “unequivocally” endorsed the CDC’s recommendation that all pregnant women receive the RSV shots in addition to the many vaccines pumped into their bodies in such a short period of time.

In truth, we need not speculate about Pfizer having the same problem as GSK, given the similarity in composition. Pfizer’s own trial data revealed the same problem with premature births.

Although the sample size was smaller, Pfizer’s phase 2 trial reported three out of 116 (2.6%) premature births in the placebo group and six out of 114 (5.3%) in the trial group. Using the trial data, Igor Chudov estimated that the shots would cause 73,288 excess preterm deaths annually in the U.S. alone, leading to several thousand additional infant deaths a year.

One pharmaceutical researcher compared GSK and Pfizer’s RSV jabs to Coke and Pepsi. Yet one will never reach the market, while the other is in every pharmacy and doctor’s office in the country. Why? $cienceTM. Let’s not forget that the NIH helped develop it and will benefit from royalties on the patent.

All of this for a virus that is rarely deadly and almost always treatable with a nebulizer. Between 2005 and 2016, RSV was identified on death certificates as the underlying cause of death for 17 babies per year on average. The fact is that no RSV vaccine known to man has proven effective and may have negative efficacy — it might do more harm than good — just as we’ve learned about the COVID shots.

Knowing all of this, will Congress continue to fund these projects in the Health and Human Services appropriations bill when the February deadline comes around? If Speaker Mike Johnson (R-La.) wants to show real leadership, he should pledge to fight for the following provisions in the bill:

  • End all funding or marketing for the COVID and RSV shots;
  • Ban on all direct-to-consumer advertising for COVID and RSV “vaccines”;
  • Repeal the protections against liability for vaccine-makers for any COVID or RSV shot, particularly for pregnant women, a provision added to the 2016 Cures Act;
  • Establish a congressional committee dedicated to researching the rationale, safety, and efficacy of all the shots the CDC currently recommends;
  • Ban the NIH from receiving royalties from any vaccine recommended by the CDC.

Republicans focus incessantly on abortion but often forget there are other spheres of the pro-life cause. We now have incontrovertible data showing that the RSV shots can be deadly for pregnancies and, in some cases, should be regarded as a chemical abortion. They should be opposed with the same rigor as we oppose abortions. Let’s leave the RSV shots to the “pregnant men.”

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COVID-19

FDA responds to Ladapo letter about DNA fragments detected in mRNA COVID-19 vaccines

In response to a letter in which Florida Surgeon General Joseph Ladapo noted the detection of DNA fragments in mRNA COVID-19 vaccines, Peter Marks, director of the U.S. Food and Drug Administration’s Center for Biologics Evaluation and Research, emphasized the FDA’s view that the shots are safe and effective.

“I am writing to you to address the recent discovery of host cell DNA fragments within the Pfizer and Moderna COVID-19 mRNA vaccines,” Ladapo noted in his letter to FDA Commissioner Robert Califf and CDC Director Mandy Cohen.

“This raises concerns regarding the presence of nucleic acid contaminants in the approved Pfizer and Moderna COVID-19 mRNA vaccines, particularly in the presence of lipid nanoparticle complexes, and Simian Virus 40 (SV40) promoter/enhancer DNA. Lipid nanoparticles are an efficient vehicle for delivery of the mRNA in the COVID-19 vaccines into human cells, and may therefore be an equally efficient vehicle for delivering contaminant DNA into human cells. The presence of SV40 promoter/enhancer DNA may also pose a unique and heightened risk of DNA integration into host cells,” Ladapo wrote.

He also noted that “it is essential to human health to assess the risks of contaminant DNA integration into human DNA.”

But when responding to Ladapo, Marks conveyed the FDA’s contention that the vaccines are safe and said that “misinformation and disinformation” causes “vaccine hesitancy that lowers vaccine uptake.”

“We would like to make clear that based on a thorough assessment of the entire manufacturing process, FDA is confident in the quality, safety, and effectiveness of the COVID-19 vaccines. The agency’s benefitrisk assessment and ongoing safety surveillance demonstrate that the benefits of their use outweigh their risks. Additionally, with over a billion doses of the mRNA vaccines administered, no safety concerns related to residual DNA have been identified,” Marks wrote.

“No SV40 proteins are encoded for or are present in the vaccines. On first principle, it is quite implausible that the residual small DNA fragments located in the cytosol could find their way into the nucleus through the nuclear membrane present in intact cells and then be incorporated into chromosomal DNA,” Marks wrote. “Additionally, studies have been conducted in animals using the modified mRNA and lipid nanoparticle together that constitute the vaccine, including the minute quantities of residual DNA fragments left over after DNAse treatment during manufacturing, and demonstrate no evidence for genotoxicity from the vaccine. Pharmacovigilance data in hundreds of millions of individuals also indicate no evidence indicative of genotoxicity.”

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2020 Election

Rudy Giuliani ordered to pay $148 million to 2 Georgia election employees over election fraud defamation

Rudy Giuliani, the former mayor of New York City, was ordered by a federal jury to pay two Georgia election workers $148 million over a defamation lawsuit related to voter fraud claims.

The jury of eight residents of Washington, D.C., deliberated for about ten hours before reaching a decision Friday afternoon.

Ruby Freeman and her daughter Wandrea ArShaye “Shaye” Moss sued Giuliani, who had represented former President Donald Trump as his personal attorney, and accused them of participating in a fake balloting scheme during the 2020 presidential election in Fulton County.

The jury awarded $16 million to Freeman for compensatory damages for defamation and awarded $17 million to Moss for compensatory damages for defamation. In addition, they awarded $20 million to each for emotional distress and $75 million in punitive damages for both.

Giuliani had previously said he would take the stand in order to testify in his defense, but he changed his mind and never testified.

“We feel like these women have been through enough,” said Giuliani’s attorney on Thursday.

Mike Gottlieb, the attorney for Moss and Freeman, argued in his closing statement that Giuliani had dehumanized the workers in order to push his narrative about the election.

“He thought they were ordinary and expendable. He didn’t see them as human beings,” said Gottlieb. “It’s dangerous for them to be Ruby Freeman or Shaye Moss because of Giuliani and his co-conspirators.”

The women testified about the numerous threats and insults they had received on social media because of the accusations made against them by Giuliani.

Giuliani later equated the damages they were seeking to “the civil equivalent of the death penalty” for the former mayor.

“They’re trying to end Mr. Giuliani,” he said to the jury.

Here’s a news report about the decision:

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COVID-19

Tucker Carlson talks COVID-19 vaccines, UFOs, and claims Alex Jones has ‘prophetic ability’

During a wide-ranging interview on BlazeTV’s “Prime Time with Alex Stein,” Tucker Carlson said that one of his friends suffered a heart attack due to the COVID-19 vaccine. He also said that Alex Jones has a “prophetic ability.” And on the topic of UFOs, Carlson suggested that “there is something that is not human flying around.”

Carlson said that his friend had been forced into taking the COVID-19 vaccine and experienced the heart attack just days later.

The prominent media personality also said “there is evidence it that it effects your DNA.”

“No, I don’t think anyone will ever be held accountable for it because it implicates too many people, because everybody took it,” Carlson said, suggesting that those who were coerced into taking the shots “feel like survivors of an assault, because they are.”

During the interview, Carlson said Jones has a “prophetic ability, which is real,” saying that Jones had “called 9/11 and did it in detail on television.” He suggested that Jones is receiving a “message from somewhere. I’m not an expert in metaphysics but … I can read the evidence and there’s no other explanation for that,” Carlson said.

When Stein asked about aliens, Carlson said “there is something that is not human flying around,” though he opined that it is not “extraterrestrial.”

“This is real. The U.S. government does have physical evidence,” which it is attempting to hide, Carlson claimed.

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Vaccines

Bill Gates and Mastercard are testing vaccine passports in Africa. Is the US next?

The Bill Gates-backed Gavi, also known as the Vaccine Alliance, Mastercard, and NGOs in the fintech space have been trialing a digital vaccine passport in Africa called the Wellness Pass. Africa has long been a testing ground for Big Pharma to test drugs and programs far from the prying eyes of journalists and regulators.

This passport, touted as a handy way to track patients in “underserved communities” across “multiple touchpoints,” is part of a grouping of consumer-facing Mastercard products aimed ostensibly at roping people into a cashless digital ID system that simultaneously automates compliance with prescribed pharmaceutical regimens and fosters dependency on at least one ideologically captive non-governmental entity.

Gavi, the leading partner and “catalyst” for the initiative, and Mastercard, “acting in the capacity of technology partner,” rolled out pilots of the Wellness Pass in Mauritania and Ethiopia under the banner of “efficiently delivering vaccines to millions of children, tracking identity and immunization records in a digitized manner and incentivizing the delivery of vaccines.”

Gavi, originally the Global Alliance for Vaccines and Immunization, has historically provided children in the third world with non-mRNA vaccinations. But its reputation and reach in relatively unregulated regions — where it has worked in recent years to limit big pharmaceutical companies’ financial risk regarding COVID-19 vaccine injuries — are now being exploited to provide cover for experimentation by Western technocrats and corporate giants.

Brazen efforts to exploit the COVID-19 pandemic in pursuit of greater power and a “new normal” have sadly cast doubt on purportedly altruistic endeavors such as this, already suspect in a region long used by pharmaceutical companies and other outfits as a sandbox for treacherous experiments.

Bill Gates’ apparent keenness to usher in a future where digital passport stamps attesting to dutiful acceptance of vaccines — including those of the kind he’s hawkish on developing in Africa — has increased suspicions that the initiative is a foretaste of efforts stateside to curb God-given freedoms.

Besides pledging more than $1.8 billion to Gavi between 2021 and June of this year, the Bill and Melinda Gates Foundation has bankrolled other similar efforts.

For instance, the foundation helped fund the World Health Organization’s 2021 “Digital Documentation of COVID-19 Certificates: Vaccination Status” guidance, which discussed the deployment of a vaccine passport “solution to address the immediate needs of the pandemic but also to build digital health infrastructure that can be a foundation for digital vaccination certificates beyond COVID-19.” It’s worth noting that the Gates Foundation provides the WHO with nearly as much financing as the U.S. government yearly.

The Gates Foundation also recently funded research into biocompatible near-infrared quantum dots indicating vaccination status, applied to the skin with microneedles. One needn’t be a biblical scholar to draw a parallel with the mark of the beast.

Despite its potentially nefarious applications, the Wellness Pass is thankfully not another Gates tattoo. Instead, more in line with the passport discussed in the WHO guidance, it is a chip card that stores a patient’s vaccine history offline.

According to Gavi, the pass, which appears to have outlived IBM’s Digital Health Pass and has the potential to give the World Economic Forum’s CommonPass app a run for its money, ensures that “vaccination records are available at any time through participating health facilities, regardless of connectivity, and utilizes tokenized biometrics when accepted, or alternatively a pin, to verify service delivery and adhere to vaccination cycles.”

The card is reportedly linked to a phone number so that jab appointment reminders can be sent.

During the pandemic, both in blue states and increasingly unfree Anglo nations like Australia and Canada, we saw vaccine receipts and QR codes become necessary to travel and use various facilities.

On the one hand, Gavi and the world’s second-largest payment processing corporation are working to ensure human test subjects are up to date on their vaccines. On the other hand, Africans appear to be unwittingly helping them beta-test improved biometric systems of control for potential deployment farther afield.

Already, bit players involved in the project have made the logical progression from the Sahara to the States. For instance, the AI-powered biometric company Trust Stamp helped incorporate its digital identification tech into the Wellness Pass system early on, then turned its focus stateside, developing applications for the American prison industry.

Gareth Genner, co-founder of Trust Stamp, said something revealing in a 2020 interview with Mastercard. Genner suggested that the hope for this technology was that “anyone in the world can say, ‘This is who I am and these are what my needs are.’”

The Wellness Pass similarly conveys identifying information and needs through what it does not say: This is what I am not; ergo these are what needs I can be denied.

During the pandemic, both in blue states and increasingly unfree Anglo nations like Australia and Canada, we saw vaccine receipts and QR codes become necessary to travel and use various facilities. Those without these prototypic vaccine passports often saw their liberties and horizons drastically limited.

An Americanized Wellness Pass, even if adopted with the pseudo-anonymized hash system used in Africa, would grant authorities similar limiting potential as before, along with a far better sense of where there were pockets of dissent, where they had to propagandize, and where there were arms yet unjabbed.

Besides helping to further shape behavior, flush out vaccine resistance, and medicalize society, such an infrastructure as Mastercard provides could lay the groundwork for the kinds of digital credentialing systems Americans have been otherwise resistive to.

Alisdair Haythornthwaite, senior vice president of thought leadership and policy communications at Mastercard, told USA Today in 2020, “There is nothing about this solution that means someone who doesn’t get vaccinated won’t get money or food.”

Sure, that might have been true of Wellness Pass as deployed in Mauritania, but time will tell what Western systems informed by these African pilot programs might ultimately accomplish in the way of prohibitions in the name of public health, climate correction, countering extremism, and so forth.

Forgive my skepticism about the beneficence of behemothic corporations, but it’s not hard to imagine soon being required to produce a Wellness Pass simply to pass go.

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Elections

New poll finds rampant mail-in voting fraud in the 2020 election

One in five voters who cast mail-in ballots during the 2020 presidential election admit to participating in at least one kind of voter fraud, according to a new poll conducted by Rasmussen Reports and the Heartland Institute.

Specifically, 21% of mail-in voters admitted they filled out a ballot for a friend or family member; 19% of mail-in voters admitted that a friend or family member filled out a ballot on their behalf; 17% of mail-in voters admitted they voted in a state where they were no longer a permanent resident; and 17% of mail-in voters said they signed a ballot for a friend or family member with or without his or her permission.

Each of these instances constitutes voter fraud.

Taking only the first instance, this means that 21% of all mail-in ballots were fraudulent in 2020. It is important to note this number was likely much higher because the survey questions were not mutually exclusive. Though there is certainly some crossover between categories, some voters committed fraud by filling out a ballot for a friend or family member, while an entirely different subset of voters committed fraud by casting mail-in ballots in a state in which they were no longer permanent residents.

The national poll of 1,085 likely voters was conducted between November 30 and December 6, with a margin of error of +/-3 percentage points and a 95% level of confidence.

Using only the most conservative estimate (21%), the number of fraudulent ballots is still astronomical. According to election data, 43% of 2020 voters cast ballots by mail — by far the largest percentage in U.S. history. Twenty-one percent of that 43% mail-in figure yields approximately 9%.

Only 0.80% of all absentee and mail-in ballots were rejected in 2020. Clearly, nearly all fraudulent ballots made it through our country’s gaping sieve of an electoral system.

According to the Cook Political Report, 158,397,726 votes were cast for Joe Biden, Donald Trump, or another candidate in 2020. Taking 9% of this total, that means more than 14 million ballots cast in 2020 were fraudulent. Again, this is just the most conservative estimate — the total number of fraudulent ballots was likely much higher.

Moreover, the survey reveals that fraudulent voting may not have been purely limited to mail-in ballots. Eight percent of all survey respondents — not only those who cast mail-in ballots — admitted that a friend, family member, or organization (such as a political party) offered to pay or reward them for voting.

The survey indicates that the percentages of voter fraud among Republicans, Democrats, and unaligned voters were largely similar. It is vital to note, however, that this does not mean these fraudulent ballots simply canceled each other out.

While the percentages were similar, the overall numbers were not. According to the survey, 38% of Biden voters submitted mail-in ballots, compared to only 23% of Trump voters. As such, Biden received a much larger overall share of likely fraudulent ballots.

The 2020 election was an outlier for mail-in voting, largely due to executive overreach throughout the COVID-19 pandemic. In the lead-up to the November election, several governors declared states of emergency in response to the pandemic and arbitrarily changed their states’ voting laws to allow mass mail-in voting. For example, California mailed unsolicited ballots to all registered voters, while many other states expanded absentee ballot eligibility requirements.

In 2020, several states also allowed ballot harvesting, which allows third-party individuals to collect and submit mail-in ballots on behalf of voters, although evidence shows ballot harvesting is “ripe for voter fraud and abuse.”

All of this occurred despite the fact that the Constitution explicitly designates that only state legislatures have the power to make or change election laws. Under Article I, Section 4, “The Times, Places and Manner of holding Elections for Senators and Representatives, shall be prescribed in each State by the Legislature thereof.”

There are many reasons why mail-in voting is less reliable than in-person voting.

For starters, state voter rolls are notoriously inaccurate. In 2012, the Pew Center on the States analyzed state voter registration rolls and found that “approximately 24 million — one of every eight — voter registrations in the United States are no longer valid or are significantly inaccurate. More than 1.8 million deceased individuals are listed as voters. Approximately 2.75 million people have registrations in more than one state.”

Mail-in ballots are also rejected at an astounding rate.

In New York, which used mail-in ballots during its primary elections in 2020, 21% of ballots were rejected due to errors. In Pennsylvania, the same scenario played out with more than 20% of mail-in ballots rejected due to voter errors.

Even NPR raised concerns about mass mail-in voting in the months before the 2020 general election.

“An extraordinarily high number of ballots — more than 550,000 — have been rejected in this year’s presidential primaries. … That’s far more than the 318,728 ballots rejected in the 2016 general election and has raised alarms about what might happen in November when tens of millions of more voters are expected to cast their ballots by mail, many for the first time,” NPR reported.

In 2012, the New York Times ran an article headlined, “Error and Fraud at Issue as Absentee Voting Rises,” which similarly concluded that “votes cast by mail are less likely to be counted, more likely to be compromised and more likely to be contested than those cast in a voting booth.”

Despite all of these concerns, only 0.80% of all absentee and mail-in ballots were rejected in 2020, according to Ballotpedia. Clearly, nearly all fraudulent ballots made it through our country’s gaping sieve of an electoral system.

Though some people need to vote by mail, the practice should be the exception, not the rule. Considering most states offer early voting — allowing voters to cast ballots in-person weeks before Election Day — there is little excuse for voters who do not show up to a physical polling location. Plus, as this poll indicates, only 2% of voters would choose not to vote if their state banned mail-in voting.

With the 2024 general election less than one year away, it is vital that state officials do everything in their power to shore up the integrity of their states’ voting systems and ensure that voting procedures are as dependable and accurate as possible. Our republic cannot survive in the absence of strong electoral laws that prevent widespread fraud.

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Elections

DC removing over 100,000 ineligible voters from ‘dirty voter rolls’ following Judicial Watch pressure campaign

The governmental transparency outfit Judicial Watch appears to have executed a successful pressure campaign to rid select voter lists of multitudes of ineligible voters in the District of Columbia.

Judicial Watch notified election officials in
D.C., California, and Illinois that they had violated the National Voter Registration Act of 1993 “based on their failure to remove inactive voters from their registration rolls.”

While officials in California and Illinois have time left to act before Judicial Watch makes good on its threat of legal action, D.C. has indicated it has already begun taking remedial steps.

The watchdog claimed in a Sept. 22
letter to the Monica Holman Evans, executive of the District of Columbia Board of Elections, that the board was in violation of Section 8 of the NVRA requiring it to “conduct a general program that makes a reasonable effort to remove the names of ineligible voters from the official lists of eligible voters for DC.”

The letter cited D.C. data provided to the U.S. Election Assistance Commission indicating zero voter registrations had been removed from November 2020 to November 2022.

According to the watchdog, EAC data showed the number of inactive registrations in the district amounted to nearly one-quarter of the total number of Washington’s registrations. Moreover, the notice stated “DC’s total registration rate — its total number of registrations divided by the most recent census estimates of its citizen voting-age population — is over 131%.”

Judicial Watch wrote, “In our experience, and as a matter of common sense, there is no possible way that the DC BOE is complying with the NVRA if it remove no registrations pursuant to that provision in a two-year period.”

The watchdog threatened to file a federal lawsuit unless the violations were corrected within 90 days.

Evans evidently blinked,
telling Judicial Watch in a letter last month that the board had taken “several list maintenance actions,” including the removal of 65,544 inactive voters on Oct. 30 who had allegedly voted in neither the 2016 nor 2020 general elections.

Evans further noted that an additional 37,962 “inactive” voters would soon be removed who had not voted in the 2018 general election, responded to address confirmation notices, or participated in the November 2022 general election.

While thousands of inactive voters were moved off the list, 73,522 voters were moved from “active to an inactive status on October 3, 2023 as a result of the 2023 biennial canvass process.”

Judicial Watch president Tom Fitton said in a statement, “Dirty voter rolls increase the potential for voter fraud.”

“As Washington, DC’s, quick cleanup of tens of thousands of names in response to Judicial Watch shows, there are potentially hundreds of thousands of names on the voter rolls that should be removed by California and Illinois,” added Fitton.

Although earlier this year, California saw over 1.2 million ineligible voters
taken off rolls in Los Angeles County, the watchdog suggested that 46 counties in the state, containing over 14 million voters, “reported removing only a handful, or no registrations under the NVRA’s change of address rules, or else failed to report any data at all.”

Illinois similarly appears to have trouble dropping ineligible voters from its lists, with 15 counties indicating zero removals from November 2020 to November 2022, according to EAC reports.

Judicial Watch also
noted in its letter to Bernadette Matthews, executive director of the Illinois State Board of Elections, that “15 Illinois jurisdictions have more voter registrations than citizens of voting age.”

It appears this is a problem for other states as well.

The Republican National Committee demanded Friday that Michigan Secretary of State Jocelyn Benson clean up her state’s voter rolls, citing a recent analysis showing 55 of Michigan’s 83 counties have more registered voters than adults 18 or older,
reported the Detroit Free Press.

“More than 50 Michigan counties have a 100% or higher rate of voter registration,” said RNC Chairwoman Ronna McDaniel.

“This is mathematically impossible and means that ineligible voters are on the rolls ahead of the upcoming 2024 election,” continued the chairwoman. “The RNC is demanding that Michigan ensure only eligible voters can vote and will take legal action to ensure that outcome if necessary.”

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COVID-19

Pfizer mRNA jab leaves 1 in 3 recipients with ‘unintended immune response’: Cambridge study

A peer-reviewed University of Cambridge
study published Wednesday in the scientific journal Nature has revealed the Nobel Prize-winning technique that paved the way for synthetic messenger ribonucleic acid vaccines is far from flawless.

To trick the body into allowing cellular interventions by synthetic mRNA-based therapeutics, scientists discovered they first had to make chemical modifications to the building blocks of the mRNA. Researchers indicated this week that encounters with repeat base modifications often lead to cellular miscommunications, which ultimately trigger immune flare-ups in vaccine recipients.

Since the mRNA technology rushed to market during the pandemic is now being used to treat various cancers and diseases, the researchers stressed the urgency of addressing this issue.

Anne Willis, a co-author of the study and biochemist from the University of Cambridge’s Medical Research Council Toxicology Unit, said it is “essential that [mRNA] therapeutics are designed to be free from unintended side effects.”

What’s the background?

Katalin Karikó and Drew Weissman were
awarded the 2023 Nobel Prize in Physiology or Medicine in October for their discoveries that enabled the development of “effective mRNA vaccines” against COVID-19.

The duo observed that the body treated synthetic mRNA — genetic material designed to tell cells in the body how to make specific proteins, such as the “spike” protein — as a foreign invader. Faced with this invader, the body would undergo an inflammatory response. This reaction proved troublesome for potential therapeutics as the body’s natural response to the synthetic material hindered its efforts to enter cells and exert its effects,
according to the University of Cambridge.

Karikó and Weissman discovered that by chemically modifying its uridine RNA base, the synthetic mRNA could steal past the body’s defenses and issue its protein schematics.

The Telegraph
reported that it was widely believed until now that the modification to uridine was unproblematic. However, it’s now clear that these covert genetic operations leave an undesired mark on a significant portion of patients subjected to the gene therapy.

Cellular miscommunication

Researchers with the MRC Toxicology Unit set out to analyze whether there were any safety issues linked to mRNA-based therapeutics. They found that “the cellular machinery that ‘reads’ mRNAs ‘slips’ when confronted with repeats of a chemical modification commonly found in mRNA therapeutics,” the university indicated in a release.

The aforementioned “cellular machinery” is called a ribosome. The ribosome reads and translates mRNA code, providing the body with instructions on how to make antibodies. When confronted with a chemical base modification of mRNA called “N1-methylpseudouridine,” ribosomes apparently slip around 10% of the time, according to Anne Willis and immunologist James Thaventhiran.

These so-called slips result in the production of unintended proteins, which set off an “unintended immune response.”

The Cambridge researchers, collaborating with scientists at other English universities, tested for evidence of the production of “off-target” proteins in vaccine recipients, specifically those who took the mRNA Pfizer COVID-19 vaccine. Sure enough, they “found an unintended immune response occurred in one third of the 21 patients in the study who were vaccinated.”

mRNA is also utilized in the Moderna vaccine, but the scientists did not report testing it for slips.

Despite the immune responses and the small sample size, the researchers claimed there were no “ill effects” as the unintended proteins produced were not viable in the body.

“The safety concern for future mRNA medicines is that misdirected immunity has huge potential to be harmful, so off-target immune responses should always be avoided,” said Thaventhiran.

The Cambridge team determined that the mRNA sequences could be redesigned to ensure the production of the intended protein and thereby avoid such unintended immune responses.

Thaventhiran, senior author of the study, issued the necessary declaration that COVID-19 vaccines are safe, then added, “We need to ensure that mRNA vaccines of the future are as reliable. Our demonstration of ‘slip-resistant’ mRNAs is a vital contribution to future safety of this medicine platform.”

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COVID-19

Florida Surgeon General Joseph Ladapo notes ‘DNA fragments detected in mRNA COVID shots’

Florida Surgeon General Joseph Ladapo, who notes that DNA fragments have been detected in mRNA COVID-19 vaccines, has issued a letter asking questions related to the issue.

“On today’s episode of: What the FDA… I asked @DrCaliff_FDA to address the DNA fragments detected in mRNA COVID shots & how they are hitchhiking into human cells. DNA integration into the human genome & oncogenesis are known risks, even acknowledged by @US_FDA in ’07,” Ladapo tweeted when sharing his letter to FDA Commisoner Robert Califf. CDC Director Mandy Cohen is also included on the letter.

In a letter earlier this year, Ladapo accused Califf and then-CDC Director Rochelle Walensky of ignoring many of the risks related to mRNA COVID-19 vaccines. In his new letter dated December 6, 2023, he noted that “no response has been received.”

“In addition to my previous letter, I am writing to you to address the recent discovery of host cell DNA fragments within the Pfizer and Moderna COVID-19 mRNA vaccines,” Ladapo noted in his new letter.

“This raises concerns regarding the presence of nucleic acid contaminants in the approved Pfizer and Moderna COVID-19 mRNA vaccines, particularly in the presence of lipid nanoparticle complexes, and Simian Virus 40 (SV40) promoter/enhancer DNA. Lipid nanoparticles are an efficient vehicle for delivery of the mRNA in the COVID-19 vaccines into human cells, and may therefore be an equally efficient vehicle for delivering contaminant DNA into human cells. The presence of SV40 promoter/enhancer DNA may also pose a unique and heightened risk of DNA integration into host cells,” he noted.

Ladapo pressed for answers to several questions, including one which reads, “Considering the potentially wide biodistribution of mRNA COVID-19 vaccines and DNA contaminants beyond the local injection site, have you evaluated the risk of DNA integration in reproductive cells with respect to the lipid nanoparticle delivery system?”

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