Wake Up America. You’ve Been Conned. Only An Estimated 9,683 Covid-19 Only Deaths So Far In 2020, Not 180,000

About half-way down the screen page The Center for Health Statistics August 26, 2020 update on provisional death counts for Coronavirus Disease 2019 (COVID-19) states the following: “For 6% of the deaths, COVID-19 was the only cause mentioned.”

Oh.  You mean America is not undergoing a pandemic?  On average, abut 8000 people die per day from all causes in the United States.  In the first 8 months of 2020 there were only ~1200 excess deaths per month or 40 extra deaths per day exclusively due to COVID-19 coronavirus infections, with 80% of those among American age 65 and older.  By extrapolation, there were only ~8 excess COVID-19 only deaths per day among working-age adults and school-age children.

Translation: of the 161,392 accumulated COVID-19 RELATED deaths reported as of August 22, 2020 (80% being among Americans age 75 and older), only 6% or ~9683 accumulated deaths were classified as COVID-19 only. Among these COVID-19 only deaths, ~60% were age 75 and older; 80% were age 65 and older. So, there were only ~2000 COVID-only deaths in working age adults and school-age children.

Sudden death epidemic: Excess mortality among young, middle-aged Americans skyrockets

If these trends continue at this same rate, it’s an absolute disaster for our economy and society at large.

Featured Image

tommaso79/Shutterstock

https://www.lifesitenews.com/author/dr-joseph-mercola/

STORY AT-A-GLANCE

  • 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.

(Mercola) – In this video, I interview repeat guest Edward (Ed) Dowd, a former analyst and fund manager with BlackRock, the largest asset manager in the world. With more than $10 trillion in assets, BlackRock wields greater financial power than any country in the world with the exception of the U.S. and China.

Dowd has a knack for seeing trends, and was able to grow the assets he managed during his time at BlackRock from $2 billion to $14 billion. Ten years ago, he left BlackRock, moved to Maui, and became an entrepreneur. More recently, he’s come out as a whistleblower against the COVID shots and Big Pharma corruption.

In our last interview, we discussed the mathematical certainty of a financial collapse, and how COVID provided a convenient smoke screen to hide this reality.

Data reveal crimes against humanity

Dowd has now published a book, “Cause Unknown: The Epidemic of Sudden Deaths in 2021 and 2022,” in which he details the data showing the shots are a crime against humanity.

“When this product [the COVID shots] came to market, I was very suspicious because I know a lot about health care” Dowd says. “I was on Wall Street and I used to analyze health care stocks. I knew that normal vaccines took seven to 10 years to prove effectiveness and safety.”

He added:

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.

That’s why I’m here, because I don’t believe anybody has a right to tell me what to do with my body, and I can’t believe this actually happened. The numbers I’m going to reveal to you are now a national security concern.

Group life insurance statistics tell a curious story

Dowd’s concerns are based on a variety of statistics, including but not limited to government mortality and disability data, as well as data from private insurance companies, such as group life insurance data. As explained by Dowd, group life policies are policies given to large Fortune 500 corporations and mid-sized companies.

Basically, when you start to work at one of these companies, you sign onto a policy from day one that includes a health care plan and life insurance plan (death benefit), which is typically one or two times your annual salary. The only way you can get a claim on these policies is if you die while employed. If you quit or get fired, you don’t get this claim.

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.

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 Extends Federal Mask Mandate

International Airport in Phoenix, Ariz., on Dec. 18, 2021. (Spencer Platt/Getty Images) The Centers for Disease Control and Prevention (CDC) has extended the federal mask mandate for transportation for two weeks, citing the small recent increase in COVID-19 cases.

Source : The Epoch Times

CDC Extends Federal Mask Mandate

People walk through Sky Harbor ICDC Extends Federal Mask Mandate

The order, which was to expire on April 18, will remain in place until May 3 to let officials at the agency assess whether the BA.2 virus subvariant drives a fresh wave of cases. “In order to assess the potential impact the rise of cases has on severe disease, including hospitalizations and deaths, and health care system capacity, the CDC order will remain in place at this time,” the CDC said in a statement.

The order was first imposed in January 2021 and applies to trains, airplanes, and other modes of transportation under purview of federal officials, as well as transportation hubs such as airports. The CDC has repeatedly extended the order, despite growing opposition to the move.

Leaders of 10 U.S. airlines in a letter last month urged the Biden administration to rescind the order, noting that COVID-19 metrics have plunged and that authorities across the country have rolled back or eliminated restrictions.

Separately, groups of pilots and flight attendants filed lawsuits against the CDC and its parent agency, alleging the mask order is unlawful.

Florida Gov. Ron DeSantis, a Republican, said in a statement that the latest extension “simply prolongs the misery that passengers and flight attendants are being forced to endure.” “This is not evidence-based, but simply more COVID theater,” he said.

The CDC’s move came after it said it would allow the expiration of Title 42, a pandemic-era order that enabled quick expulsion of illegal immigrants because they might carry the virus that causes COVID-19.CDC Director Dr. Rochelle Walensky said the action was taken because COVID-19 cases fell by over 95 percent between January and March and because more of the population has some form of immunity from vaccination and/or prior infection.According to data reported to the CDC, about 36,300 COVID-19 cases were recorded on April 11. That was a slight increase from the week prior.COVID-19-related hospitalizations and deaths are also relatively flat after bottoming out following January’s peaks.Some experts pin the rise in cases on BA.2, a subvariant of the Omicron strain of the CCP virus, which causes COVID-19.White House COVID-19 coordinator Ashish Jha had said earlier this week that a mask mandate extension was “absolutely on the table” but that it would be up to the CDC whether to allow the mandate to expire or extend it once again