There’s a “Died Suddenly” Epidemic…One Expert Went Through the Data and Reveals The “Coverup”

I don’t need to tell you that there’s a problem. You can see what’s happening with your own eyes. Over the past year or so, there has been a strangely large number of healthy, young people who are “dying suddenly.” These poor people are dropping like flies at an alarming rate. At first, stories of young, healthy people “dying suddenly” were peppered here and there, but now, there are so many of these stories, that I can’t keep up with them. And just imagine how many of these “sudden deaths” aren’t being talked about in the media.

Scary thought. 

Well, it’s gotten so bad, that people are now taking notice and talking about the “Died Suddenly” phenomenon. And one of those people is a former BlackRock fund manager who has poured through the data and what he found, is startling.

Lifestite reported that in his new book, “Cause Unknown: The Epidemic of Sudden Deaths in 2021 and 2022,” former BlackRock fund manager Edward Dowd details data showing the COVID shots are a crime against humanity.

Insurance industry research in 2016 concluded that group life policyholders die at one-third the rate of the general U.S. population, so they’re the healthiest among us. Group life policyholders are those employed with Fortune 500 companies, who tend to be younger and well-educated.

In 2020, the general U.S. population had higher excess mortality than group life holders, but in 2021, that flipped. Ages 25 through 64 of the group life policyholders suddenly experienced 40 percent excess mortality, compared to 32 percent in the general population. In short, a far healthier subset of the population suddenly died at a higher rate than the general population.
American disability statistics are equally revealing. In the five years before COVID, the monthly disability rate was between 29 million and 30 million. After the COVID jabs, the disability trend changed dramatically. As of September 2022, there were 33.2 million disabled Americans ­– an extra 3.2 million to 4.2 million – a three standard deviation rate of change since May 2021.

Since May 2021, the overall U.S. population has experienced an 11 percent increase in disabilities, while the employed – which is about 98 million out of a total population of about 320 million – experienced 26 percent increased rate of disability. So, something was introduced into the workforce that caused working age people to die.

Edward Dowd goes on to say:

This was an experimental vaccine, a non-traditional gene therapy that had never been tested on humans. I read the literature on the animal tests and they were an abomination. Then, this thing was approved in 28 days. They got rid of the control group. I knew it was Operation Warp Speed, so I was highly suspicious of this whole thing from the get-go.

Then in early 2021, I started hearing anecdotes that people were getting sick and/or injured, or died, from distant friends and relatives. I started reading about sudden athlete deaths, [and] suspected the vaccine right away. I didn’t have the data that I have now, but I said to myself, ‘You know, I’m going to look at insurance company results, funeral home results.’

That eventually led to excess mortality statistics… I’m known as ‘the excess mortality guy’ right now. What I’ve learned through my own personal experience is that Pharma is, on the whole, mostly fraudulent. Most drugs that have been approved by the FDA [U.S. Food and Drug Administration] aren’t really all that safe and effective.

They have to recall so many drugs every year. The FDA has been wholly captured by the pharma industry. 70 to 75 percent of the drug approval pharma arm of the FDA comes from pharma fees, directly from the companies, so this has been corrupted for a long time.

It’s now exposed primarily because [the COVID shot] is [injuring and killing] such a large amount of people. It’s hard to hide this one… This fraud is unveiled and out there for people to see, but it’s only in the echo chamber. Mainstream media is still beholden to Big Pharma because of all the ad spend and the government policymakers… [who] want this to go away.

There’s a giant cover-up going on as far as I’m concerned. The data that I’m going to talk about today is there for the global health authorities to see. They see what I see, and at this point it’s negligence, malfeasance, a cover-up and a crime.

I really encourage you to read the entire piece over at Lifesite. Click here.

Flashback: Fauci’s NIH funded experiments on AIDS orphans in New York City

Flashback: Fauci’s NIH funded experiments on AIDS orphans in New York City

Incarnation Children’s Center (ICC) “began testing drugs on its orphan population in 1992

by WorldTribune Staff, October 26, 2021

Dr. Anthony Fauci’s National Institutes of Health (NIH) approved drug trial experiments on hundreds of AIDS orphans in New York City. Over 200 of the orphans died during or after the experiments, according to Liam Scheff, the investigative reporter who broke the story.

The Incarnation Children’s Center (ICC) “began testing drugs on its orphan population in 1992, the same year they became a subsidiary of Columbia University’s Pediatric AIDS Clinical Trial Unit, under Dr. Anne Gershon,” Scheff noted. “In 2003, I went undercover inside the facility and saw the effects of the drugs on the children myself.”‘These children were, because of their HIV status, written off as a loss by the medical authority, before they even got a chance to live.’

Scheff broke the story in an article entitled The House that AIDS Built that first ran on Indymedia.org.

Scheff said his investigation found that the NIH and Columbia Presbyterian Hospital acted unethically.

The Associated Press reported in June 2005: “The government has concluded at least some AIDS drug experiments involving foster children violated federal rules designed to ensure vulnerable youths were protected from the risks of medical research.”

Fauci was the NIH AIDS Coordinator before being appointed as the first Director of the Office of AIDS research when the office was established in 1988. He served in that capacity until 1994. Fauci became director of the National Institute of Allergy and Infectious Diseases (NIAID) in 1984 and still holds that position.

Scheff reported several deaths in children at the ICC during the drug trials, adding that “although the mainstream denied that any deaths were due to drug toxicity, they admit that over 200 children died.”

In 2005, the City of New York hired the VERA Institute to produce a final report on the drug trials. VERA was given no access to medical records for any of the children used in trials. Their report was published in 2008.

VERA reported that 25 children died during the drug studies, that an additional 55 children died following the studies (in foster care), and, according to Tim Ross, Director of the Child Welfare program at VERA (as of 2009), 29 percent of the remaining 417 children who were used in drug studies had died (out of a total 532 children that are admitted to have been used).

No payment or compensation was ever paid to any of the children used in the trials, or to their families, Scheff noted.

Many of the drugs (like AZT and its analogues) that were used in the experiments on the AIDS orphans in New York City had previously been approved for use in adults and “evidenced life-threatening and fatal toxicities,” Scheff reported. “So why put a drug with severe recorded toxicities into a population of black and Hispanic orphans?”

Scheff noted: “Incarnation’s orphans live at the bottom of the American class system. Often the children of drug users, they were born into ill health and poverty. Additionally (and like all AIDS patients), these children were, because of their HIV status, written off as a loss by the medical authority, before they even got a chance to live.”

Anthony Fauci

Why wasn’t Fauci’s NIH interested in competitive AIDS research?

“That’s the billion-dollar question,” Scheff noted. “That is, if inexpensive micronutrients and competitive disease and treatment models prove more successful than the current research, it will represent a loss of billions for the AIDS drug and research industry.”

mRNA Vaccines and EUA

open.substack.com/pub/rwmalonemd/p/mrna-vaccines-and-eua

mRNA Vaccines and EUA by Dr. Robert Malone

Whatever you may currently think about the SARS-CoV-2 vaccines, it is a fact that more than 5.41 billion people worldwide have received a dose of some type of COVID-19 vaccine, equal to about 70.5 percent of the world population.  In the United States as of October 17, 2022, 494.74 million “initial protocol doses” of SARS-CoV-2 vaccine have been administered, together with 138.16 million “booster” doses. 265.59 million US residents have received at least one dose, and 226.59 million have completed the initial vaccination protocol (see this link), out of a total population of 335.49 million (67.5%). In terms of the logistics of development, manufacturing and deployment of a novel injectable biologic product, this is undeniably a major achievement.

Of the SARS-CoV-2 mRNA vaccine doses administered in the United States as of October 19, 2022:

375.64M doses of Pfizer/Bio-N-Tech 237.61 doses of Moderna

Total U.S. of 613.25M mRNA vaccine doses administered. 

In the European Union, the corresponding numbers are:

641.89M doses of Pfizer/Bio-N-Tech 153.16M doses of Moderna

EU total of 795.05M mRNA vaccine doses administered

Grand Total of 1 Billion

408.3 million doses of mRNA vaccines in these two regions. All this involves a novel technology, product and large scale manufacturing process which was created, passed non-clinical and clinical development and was massively manufactured, distributed and globally deployed in less than three years.

At a meeting of the Special Committee of the European Union Parliament held on 11 October 2022 to discuss the findings regarding COVID-19 pandemic and recommendations for the future, a Pfizer executive confirmed that the vaccine had never been tested for its ability to prevent the transmission of SARS-CoV-2 virus before being put on the market. Data emerging since the introduction of the vaccine indicates that it is in fact unable to do so, thereby refuting the claim that the COVID-19 Passports provide any guarantee of protection.  In other words, although governments throughout the world employed a wide range of propaganda and censorship methods to promote these products as both safe and effective at stopping the spread of SARS-CoV-2 infection, there were no studies performed prior to this distribution which even tested how well the products would prevent the spread of COVID-19 disease.  It is not an exaggeration to state that this massive deployment has been the largest clinical experiment performed on human beings in the history of the world. 

All of the mRNA vaccine doses administered in the United States (to both citizens and military personnel) have been provided under “Emergency Use Authorization” (EUA), which is to say that although the FDA has licensed the Pfizer/Bio-N-Tech and Moderna vaccines for some age cohorts, the firms have elected to not manufacture, distribute, or market these licensed products in the United States.  The reason for this is not clear, but appears to relate to both liability issues as well as conditions placed by the FDA involving additional clinical studies, safety monitoring (pharmacovigilance)  and product disclosures once the products begin to be marketed.

From the standpoint of the vaccine manufacturers, EUA is a preferred pathway for marketing their products.  A single purchaser (the US Government) provides complete liability indemnification, a guaranteed market with very little oversight, and manages both the distribution and marketing.  In the case of all unlicensed products, the manufacturers are prohibited from marketing them, but under EUA the US Government has been doing this for them, and has been acting in coordination with corporate media, social media, and large technology firms to suppress any discussion of risks or limitations of the products.  From the standpoint of the vaccine manufacturers, this is all profit and no risk; a perfect business model.  Why would they ever want to consider taking up the burden of actually producing and marketing the licensed version of these products?

EUA is a process defined by US federal law (21 U.S. Code § 360bbb–3 – Authorization for medical products for use in emergencies) which in the case of these mRNA-based products involves biological products which are not approved, licensed, or cleared for commercial distribution.  Specifically, the statute authorizes “the introduction into interstate commerce, during the effective period of a declaration under subsection (b), of a drug, device, or biological product intended for use in an actual or potential emergency.”  Continued “Emergency Use Authorization” of these vaccines requires “a determination by the Secretary of Homeland Security that there is a domestic emergency, or a significant potential for a domestic emergency, involving a heightened risk of attack with a biological, chemical, radiological, or nuclear agent or agents”. Once the domestic emergency has passed (ergo “a determination by the Secretary, in consultation as appropriate with the Secretary of Homeland Security or the Secretary of Defense, that the circumstances described in paragraph (1) have ceased to exist”),  “A declaration under this subsection shall terminate”.  In other words, when there is no longer an emergency, the “Emergency Use Authorization” for the product will cease, and the vaccine products will return to their status as not approved, licensed, or cleared for commercial distribution.  These products remain experimental, and are only to be used for a limited amount of time during an ongoing emergency. 

“Pseudouridine likely affects multiple facets of mRNA function, including reduced immune stimulation by several mechanisms, prolonged half-life of pseudouridine-containing RNA, as well as potentially deleterious effects of Ψ on translation fidelity and efficiency.”

Based on the currently available information, it appears to me that the extensive random incorporation of pseudouridine into the synthetic mRNA-like molecules used for the Pfizer/BioNTech and Moderna SARS-CoV-2 vaccines may well account for much or all of the observed immunosuppression, DNA virus reactivation, and remarkable persistence of the synthetic “mRNA” molecules observed in lymph node biopsy tissues (Roltgen et al. 2022). Many of these adverse effects were reported by Kariko, Weissman et al in their 2008 paper  “Incorporation of pseudouridine into mRNA yields superior nonimmunogenic vector with increased translational capacity and biological stability” (Kariko et al. 2008) and could have been anticipated by regulatory and toxicology professionals if they had bothered to consider these findings prior to allowing emergency use authorization and widespread (global) deployment of what is truly an immature and previously untested technology.  Therefore, neither the FDA, NIH, CDC, nor BioNTech (which employs Dr. Kariko as a Vice President) nor Moderna can claim true ignorance.  To my eyes, what we have seen is more appropriately classified as “willful ignorance”.

Based on my review of the scientific data, it is my opinion that the random and uncontrolled insertion of pseudouridine into the manufactured “mRNA”-like molecules creates a population of polymers which may resemble natural mRNA, but which have a variety of properties which are clinically relevant. These characteristics and activities may account for many of the unusual effects, unusual stability, and striking adverse events associated with this new class of vaccines. These molecules are not natural mRNA, and they do not behave like natural mRNA. 

The question that most troubles and perplexes me at this point is why the biological consequences of these modifications and associated clinical adverse effects were not thoroughly investigated before widespread administration of random pseudouridine-incorporating “mRNA”-like molecules to a global population. 

Biology, and particularly molecular biology, is highly complex and interrelated.  Change one thing over here, and it is really hard to predict what might happen over there. That is why one must do rigorously controlled non-clinical and clinical research. Once again, it appears to me that the hubris of “elite” high status scientists, physicians and governmental “public health” bureaucrats has overcome common sense, well established regulatory norms have been disregarded, and patients have unnecessarily suffered as a consequence.  These products do not use natural mRNA, and referring to them as mRNA vaccines is misleading.  I recommend that, in the future, these products which employ a synthetic unnatural polymer which is not natural mRNA, should be designated using a different term, such as Ψ-mRNA genetic medicines.

CDC reports fewer COVID-19 pediatric deaths after data correction

The U.S. Centers for Disease Control and Prevention reported 966,575 deaths from COVID-19 on Friday after it corrected the data earlier this week, which reduced the death tallies in all age-groups, including children.

The health agency, in a statement to Reuters, said it made adjustments to its COVID Data Tracker’s mortality data on March 14 because its algorithm was accidentally counting deaths that were not COVID-19-related.

The adjustment resulted in removal of 72,277 deaths previously reported across 26 states, including 416 pediatric deaths, CDC said.

The reduction cut the CDC’s estimate of deaths in children by 24% to 1,341 as of March 18.
— Read on news.yahoo.com/cdc-reports-fewer-covid-19-204027980.html

Kakistocracy: noun, government by the worst persons; a form of government in which the worst persons are in power

Kakistocracy: noun, government by the worst persons; a form of government in which the worst persons are in power.

The old saying goes that even a blind squirrel finds a nut occasionally.  So you might think that during a 50-year political career, the odds would dictate that Joe Biden would, once in a blue moon, make a correct decision — just based on the odds.  But you’d be mistaken.  Biden has stumbled and bumbled from one disastrous decision to the next.  Disastrous, that is, for America.  Biden himself has prospered handsomely in spite of his glaring incompetence and corruption. 

Biden’s long Senate career was based on being the credit card companies’ man in Washington.  While crowing endlessly about the working class being “his people,” Biden sponsored bills allowing bank issuers to charge egregious interest rates and to make it harder for working men to escape the credit trap through bankruptcy.

When Biden chaired the Senate Judiciary Committee, he turned the confirmation of Clarence Thomas into a political smear campaign that descended into a degenerate three-ring circus. In his first campaign for president, he failed to garner a single percentage point before having to withdraw when confronted with his past lies and blatant plagiarism. He literally stole a speech detailing a British politician’s life story. He ran again in 2008 but again failed to reach even one percent of the vote.

When Barack Obama took him off the primary trash heap to make him vice president, Biden first made a hash out of the 2009 American Recovery and Reinvestment Act, wasting hundreds of billions on boondoggles and giveaways to Democrat cronies. Little of the recovery billions was spent on anything useful to America. Biden went on to manage our relations with China and Ukraine, pocketing untold millions for himself and his family by selling out America’s security interests.

By the time he ran for president again in 2020 he was a spent husk of his former corrupt and incompetent self, delivering asinine performances in the Iowa caucus and New Hampshire primary. When the Democrat establishment propped him up to once again stop Bernie Sanders, Biden was set up for the strangest presidential campaign in modern history. While Donald Trump barnstormed the nation with packed, enthusiastic rallies, Biden cowered in his basement, occasionally venturing out to speak with a few dozen voters sitting in circles drawn on the floor.

For his vice presidential pick, he chose — if you can believe it — an even more buffoonish candidate than himself.

Had it not been for Mark Zuckerberg buying and staffing government election offices in swing states, and the media and Big Tech’s censorship of the Biden family’s corruption, Biden would now be enjoying his dotage in Delaware, creeping on unsuspecting children with yarns of Corn Pop and South African arrests.

Instead, the man with one of the most astonishing records of abject failure in Washington was installed in the White House, and he has remained true to form.  As one of a hundred senators and then as vice president, there was a limit to how much damage he could do.  But as president, the shackles have been removed.

His first agenda item was to throttle our oil and gas sector, offshoring tens of thousands of good paying jobs to Russia and the Middle East — along with our energy independence. He threw open our southern border and encouraged virtually unlimited illegal immigration — during a global pandemic.

He sponsored trillions of dollars in wasteful spending, pushing our national debt to over $31 trillion.  Were it not for two Democrat senators who had not yet taken leave of their senses, it would have been even worse.  As it is, Biden has sparked the largest one-year increase in inflation in 40 years.

Biden’s “defund the police” rhetoric delivered us soaring violent crime in Democrat-run cities, while he sicced federal law enforcement on parents who object too strenuously to their children being indoctrinated with anti-White racism and LGBTQIA+ ideology. 

It can truly be said that as president, Biden’s record of failure remains unblemished.  

But now comes what may be the capstone on Biden’s long history of buffoonery and corruption.  In Ukraine, we have an armed conflict that threatens to plunge the world into an economic depression and raises the specter of nuclear war.  Not only did Biden set the stage for this calamity when, as vice president, he was in charge of Ukraine policy and led Kiev to believe that NATO membership was in Ukraine’s future, but on the eve of the Russian invasion, he refused to admit that it was not.  Then Biden all but admitted to Vladimir Putin — on live TV, no less — that NATO would not defend Ukraine if Russia chose to invade. 

In the aftermath of Russia’s invasion, Biden and his administration have crafted sanctions that seem almost designed to boomerang on America’s and Europe’s fragile post-pandemic economies, while forcing Russia into a deeper alliance with China

With the U.S. over $31 trillion in debt, Biden seems totally oblivious to the perilous position of the U.S. dollar as the world’s reserve currency and the consequences should that privileged position end. 

Economists predict that food and gasoline will cost the average U.S. household an additional $3,000 this year, and inflation threatens to push millions of lower-middle income-earners into abject poverty.

And bumbling, corrupt Joe Biden isn’t yet halfway through his first — and please God, last — term.

Image: Gage Skidmore via Flickr, CC BY-SA 2.0.
Image: Gage Skidmore via Flickr, CC BY-SA 2.0.

Image: Gage Skidmore via Flickr, CC BY-SA 2.0.

Jim Daws is a recovering talk radio host at jimdaws.com.

Big Tech Censored Dozens of Doctors, More Than 800 Accounts for COVID-19 ‘Misinformation,’ Study Finds

Resource : https://www.bloomberg.com/press-releases/2022-02-08/merck-and-ridgeback-announce-that-3-1-million-courses-of-molnupiravir-an-investigational-oral-antiviral-covid-19-medicine-have

Big Tech Censored Dozens of Doctors, More Than 800 Accounts for COVID-19 ‘Misinformation,’ Study Finds

Ailan Evans / @AilanHEvans / February 09, 2022

Twitter, Google, Google+, Gmail, Facebook, Instagram, and Snapchat are among the platforms arrayed on the screen of an Apple iPhone. Many of them have used their largely unregulated power to censor information they don’t approve of as “misinformation.” (Photo: Chesnot/Getty Images)

Major technology companies and social media platforms have removed, suppressed or flagged the accounts of more than 800 prominent individuals and organizations, including medical doctors, for COVID-19 “misinformation,” according to a new study from the Media Research Center.

The study focused on acts of censorship on major social media platforms and online services, including Facebook, YouTube, Instagram, Twitter, LinkedIn, Google Ads, and TikTok.

dailycallerlogo

Instances of censorship included Facebook’s decision to flag the British Medical Journal with a “fact check” and “missing context” label, reducing the visibility of a post, for a study delving into data-integrity issues with a Pfizer vaccine clinical trial.

Facebook also deleted the page of the Great Barrington Declaration, an open letter led by dozens of medical professionals, including Dr. Jay Battacharya, a Stanford epidemiologist, and Dr. Martin Kulldorff, a former employee of the Centers for Disease Control and Prevention, which advocated for less restrictive measures to address the dangers of COVID-19.

“Big Tech set up a system where you can’t disagree with ‘the science’ even though that’s the foundation of the scientific method,” Dan Gainor, MRC vice president of Free Speech America, told the Daily Caller National Foundation. “If doctors and academic journals can’t debate publicly, then it’s not science at all. It’s ‘religion.’”

Big Tech also scrubbed podcast host Joe Rogan’s interviews with scientists Dr. Peter McCullough and Dr. Robert Malone, the latter of whom was instrumental in pioneering mRNA technology. Twitter banned Malone from its platform permanently in late December over the virologist’s tweets questioning the efficacy and safety of the COVID-19 vaccine.

“We tallied 32 different doctors who were censored, including mRNA vaccine innovator Dr. Robert Malone,” Gainor said. “Censoring views of credentialed experts doesn’t ensure confidence in vaccines. It undermines faith in government COVID-19 strategies.“

In addition to medical doctors, the study examined instances in which members of Congress were censored by tech platforms.

These included an incident last August in which YouTube suspended Sen. Rand Paul, R-Ky., for posting a video arguing that “cloth masks” are not effective against the coronavirus, a view later echoed by many prominent medical commentators. Twitter also flagged a tweet from Rep. Thomas Massie, R-Ky., in which he wrote “studies show those with natural immunity from a prior infection are much less likely to contract and spread COVID than those who only have vaccine-induced immunity.”

The study also examined Big Tech censorship of prominent media personalities, such as Rogan, Tucker Carlson, and Dan Bongino.

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YOU MUST FIGHT FOR YOUR FAMILY IN HOSPITALS

YOU MUST FIGHT FOR YOUR FAMILY IN HOSPITALS

– Attorney Renz

Attorney Thomas Renz speaking at Clay Clark’s ReAwaken America Tour in Michigan says he is constantly contacted by families across America who have loved ones being killed by the hospital protocols that Fauci instituted in all US hospitals. The Remdesivir + Ventilator protocol finds people dying, and hospitals making Covid money. You have Medical Rights!

CLICK HERE OR ON THE PHOTO BELOW TO VIEW VIDEO

Click photo to watch
You Must Fight For Your Families in Hospitals

During this speech Attorney Renz gives you several key pieces of information on how to fight hospitals and why you must fight for your family members.

1- Do not let the hospitals isolate your family members from you.

2 – Remdesivir and Ventilators equal death for your hospitalized family member. That is the Fauci protocol.

3 – Remdesivir and Ventilators equal death is key.

Ivermectin, Hydroxychloroquine, and Budesonide work.

Go here for protocols that work:
The Math+ and I-Mask+ protocols that Renz references in his speech are here:

FRONT LINE COVID-19 CRITICAL CARE ALLIANCE
PREVENTION & TREATMENT PROTOCOLS FOR COVID-19

https://covid19criticalcare.com/covid-19-protocols/

Another great treatment resource is PATIENT TREATMENT GUIDE E-BOOKLET AND DOWNLOAD PAGE. https://www.truthforhealth.org/patient-treatment-guidehttps://www.truthforhealth.org/patient-treatment-guide