Ex-CDC Director Says It’s High Time To Admit ‘Significant Side Effects’ Of COVID-19 Vaccines

Dr. Robert Redfield, former director of the Centers for Disease Control and Prevention (CDC), said Thursday that many officials who tried to warn the public about potential problems with COVID-19 vaccines were pressured into silence and that it’s high time to admit that there were “significant” side effects that made people sick.

Dr. Redfield made the remarks in a May 16 interview with Chris Cuomo on NewsNation, during which he lamented the loss of public confidence in public health agencies because of a lack of transparency around the vaccines, which he said “saved a lot of lives” but also made some people “quite ill.”

Those of us that tried to suggest there may be significant side effects from vaccines … we kind of got canceled because no one wanted to talk about the potential that there was a problem from the vaccines, because they were afraid that that would cause people not to want to get vaccinated,” Dr. Redfield said.

In his role as head of the CDC, Dr. Redfield was part of the Trump administration’s Operation Warp Speed, a project to surge COVID-19 vaccine development at a time during the pandemic when little was known about the virus and rapid vaccine rollout was widely seen as key to getting the outbreak under control and lockdowns lifted.

In September 2020, a few months before the first COVID-19 vaccines were given in the United States, Dr. Redfield testified before the Senate that COVID-19 represented the “most significant public health challenge to face our nation in more than a century,” and that the prevailing view among scientists at the time was that the overall case fatality rate of the disease was somewhere between 0.4 and 0.6 percent in the United States.

If you were to look right now, individuals under the age of 18, it’s about 0.01 percent, 19 to say 69, it’s more like 0.3 percent. And if you’re over the age of 70, it’s about 5 percent now,” he testified at the time.

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Pfizer’s Covid Gene Therapy Shots Have Over 500 Times Allowable Levels of DNA Contamination — Study

study published this month has found that the Pfizer mRNA Covid ‘vaccine’ gene therapy injections contain DNA contamination at over 500 times allowable levels, raising fears that the DNA may integrate into the vaccinated person’s own DNA, causing mutations that can lead to diseases such as cancer.

“The available information and data indicate that the ready-to-use mRNA vaccine Comirnaty contains DNA impurities that exceed the permitted limit value by several hundred times and, in some cases, even more than 500 times,” the study said in the ‘Conclusions’ section.

Modified messenger RNA (mRNA) vaccines work by encapsulating the RNA sequence of the Covid spike protein (the dangerous part of Covid, linked to HIV) into lipid nanoparticles which are able to deliver the RNA payload into the body’s cells. The RNA is then integrated into the person’s genetics so they will produce the Covid spike protein, which the body can then develop an immune response to.

However, according to the study, mRNA is not the only genetic information being injected into people.

“…in addition to the mRNA active ingredient, DNA impurities are also encased in lipid nanoparticles and are therefore difficult to quantify,” the study said in the ‘Abstract’ section.

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Covid Fearmongering Worked So Well, The Government Is Now Creating A Poultry Panic

In 2020, the supply chain experienced disruptions that no one in my generation had ever seen. It became even more apparent to those who believe in the power of self-reliance that it is up to us to take care of ourselves. Backyard farming began booming, along with an increased interest in raising chickens.

Since then, efforts to balance self-sustainable lifestyles have been threatened. Government interference in normal healthy practices continues to grow amid concerns over “public safety.”

During the pandemic, my family added fruit trees to our already-growing vegetable garden and discussed getting chickens. It offered a sense of peace in a time of unprecedented government overreach.

The years to come offered plenty of related concerns. In 2022, the U.S. Department of Agriculture (USDA) unveiled its “People’s Garden Initiative.” This encouraged Americans to register their backyard, school, and community gardens and is still being presented as a beneficial collaboration.

But if you read the full breakdown, it advances “equity” and other “DEI” and Green New Deal initiatives that reek of a government takeover. I, like many other Americans who value their freedoms, have not registered my garden because my food belongs to me and is no one else’s business.

Now as avian flu is making headlines, fears that “they’re coming for your chickens” are being realized.

Although the Centers for Disease Control (CDC) admits that “the current public health risk is low,” it also posted that more than 90 million detections have been found in wild birds and backyard and commercial flocks across 48 states.

Yet, in the fine print, they note that this number was compiled over a two-year period and offer no information on how the testing was administered, how deadly the virus is, or how many birds have recovered.

So once again, the numbers are being stacked to breed fear. Why?

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NIH official finally admits taxpayers funded gain-of-function research in Wuhan — after years of denials

It’s about time!

At long last, National Institutes of Health (NIH) principal deputy director Lawrence Tabak admitted to Congress Thursday that US taxpayers funded gain-of-function research at the Wuhan Institute of Virology in China in the months and years before the COVID-19 pandemic.

“Dr. Tabak,” asked Rep. Debbie Lesko (R-Ariz.) of the Select Subcommittee on the Coronavirus Pandemic, “did NIH fund gain-of-function research at the Wuhan Institute of Virology through [Manhattan-based nonprofit] EcoHealth [Alliance]?”

“It depends on your definition of gain-of-function research,” Tabak answered. “If you’re speaking about the generic term, yes, we did.”

The response comes after more than four years of evasions from federal public health officials — including Tabak himself and former National Institute of Allergy and Infectious Diseases (NIAID) director Dr. Anthony Fauci — about the controversial research practice that modifies viruses to make them more infectious.

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Marathon Runner Left Disabled By AstraZeneca Covid Jab Now Suing Company, But UK Taxpayers To Foot Bill

A 50-year-old UK man named Adrian Walker was left disabled after taking the AstraZeneca Covid shot, and now he’s part of a class-action lawsuit against the company.

This comes as the pharmaceutical giant takes its COVID-19 jab off the market worldwide due to health hazards.

However, even if the 51 people pursuing legal action against the company are successful in court, AstraZeneca will be financially off the hook as the UK government gave the company legal immunity during the pandemic.

Because of the government’s deal with AstraZeneca, and other Covid jab manufacturers, UK taxpayers will instead foot the bill.

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Coronavirus Pandemic Select Subcommittee Moves Closer To The Covid-19 Origin Coverup To Protect Anthony Fauci

The House Select Subcommittee on the Coronavirus Pandemic sent a subpoena Wednesday to compel Dr. David Moreno to testify in a public congressional hearing on May 22 before Anthony Fauci’s scheduled public hearing on June 3. 

Just like the National Institute of Health (NIH) and National Institute of Allergy and Infectious Diseases (NIAID) officials, like Dr. Francis Collins and Dr. Anthony Fauci, wanted to create the narrative that vaccinations were the only answer to COVID-19 pandemic in order to lift the lockdowns, and worked overtime to not create vaccination hesitancy by pushing the false narrative that COVID-19 vaccinations were “safe and effective” for all, congressional investigators are slowly unraveling how many players also are working overtime to protect Anthony Fauci over the COVID-19 origins. It is of no surprise that Dr. Peter Daszak of EchoHealth Alliance is involved, as is his mentor, Dr. David Moreno, who was Fauci’s Senior Scientific Advisor at NIAID, who was put on administrative leave in 2023. 

Congressman Brad Wenstrup (R-OH), Chairman of the Select Subcommittee, lowered the boom Wednesday by sending the subpoena to Morens after the subcommittee uncovered evidence suggesting Morens intentionally obstructed the investigations into the origins of COVID-19.

In June 2023, Morens tried to avoid potential Freedom of Information Act (FOIA) requests by using his personal email instead of his NIH email, a letter from Wenstrup reads. Lawmakers have been asking if documents have been destroyed.

After the subcommittee discovered Morens’ potential federal records violation, the NIH placed Morens on administrative leave.

In October 2023, Wenstrup announced a subpoena for NIH records related to Morens’ potential federal records violation. NIH conducted an internal investigation into Morens’ actions but did not share its findings with Capitol Hill.

In November 2023, EcoHealth Alliance President Peter Daszak appeared for a transcribed interview and called Morens a “mentor.”

In December 2023, Morens was scheduled to appear for a transcribed interview. The Department of Health and Human Services (HHS) stepped in and prohibited Morens from answering any questions about the origins of COVID-19. 

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Classified docs from State Dept. give more credence to Covid-19 Chinese lab leak

The House Select Subcommittee on the Coronavirus Pandemic recently reviewed classified State Department documents that credibly suggest Covid-19 originated from a lab related accident in Wuhan, China.

Many experts said this was the case from the start of the pandemic but were censored by the US government, media, and social media.

The lab and research at issue, controversial “gain of function” studies to develop new vaccines, were funded with US taxpayer money via Dr. Anthony Fauci’s National Institute of Allergy and Infectious Diseases.

The documents also strongly convey that the Chinese Communist Party attempted to cover-up the lab leak and that the Wuhan Institute of Virology (WIV) maintains a relationship with the Chinese People’s Liberation Army (PLA), according to the members of Congress.

Of course this is no surprise since it has long been known that all research in China is looked at with a civilian and a separate military purpose in mind.

Rep. Brad Wenstrup (R-Ohio) is requesting the State Department rapidly declassify this information and share it with the American people.

These documents were previously released in an unclassified and highly redacted Freedom of Information Act production, first obtained and reported on by US Right to Know — a nonprofit working to expose government failures that threaten public health.

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Woman With Vaccine Injury in Clinical Trial Sues AstraZeneca

An American woman who suffered an injury from AstraZeneca’s COVID-19 vaccine sued the company on May 13, alleging the company breached a contract by not paying for the medical care she requires to deal with the injury.

“They left us no choice,” Brianne Dressen, a preschool teacher in Utah, told The Epoch Times in an email.

Ms. Dressen has paid tens of thousands of dollars to drugs to treat the nervous system disorder and other issues she’s experiencing, according to the complaint, filed in federal court in her home state.

Ms. Dressen chose to participate in AstraZeneca’s clinical trial in 2020 because she wanted to help the company develop its COVID-19 vaccine. The consent form she signed stated in part that AstraZeneca would “cover the costs of research injuries” and “pay the costs of medical treatment.”

“With these reassurances should something go wrong, Bri signed the form, rolled up her sleeve, and let the drug company inject the experimental product into her arm. Her mind was at peace, as Bri believed she was doing the right thing for her country, her students, and her family,” the suit states.

Ms. Dressen soon started experiencing problems, including blurred vision, tinnitus, and vomiting. She later became extremely sensitive to light and suffered spikes in her heart rate.

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CDC forced to release V-safe data, which includes over 780,000 reports of adverse reactions to Covid-19 shot

Reports of Covid-19 shot-related health problems, which were collected and kept hidden by the U.S Centers for Disease Control and Prevention (CDC) for several years, have now been published and reveal serious immune and brain dysfunction symptoms, include heart inflammation and death. Information on about 780,000 reports of adverse events following Covid shots were gathered and stored in the CDC’s special V-safe monitoring system that enabled Covid shot recipients to report adverse events via a cell phone text message.

V-safe is a smart-phone based surveillance system that allows users to access web-based surveys monitoring Covid shot adverse events and report reaction symptoms via a text message to federal health officials.

In the weeks after getting a Covid shot, V-safe users receive daily text messages asking about their health status. The messages contain a link to V-safe that allows users to answer follow-up questions including a checkbox of 12 symptoms, as well as enter a description of adverse events in a text message of not more than 250 characters.

According to a Jan. 13, 2024 article in The Epoch Times, CDC officials have collected approximately 7.8 million text responses from Covid shot recipients through V-safe. 

Previously, the CDC denied the public access to the V-safe reports and instead reported studies alleging that the data collected showed the shot was safe.

V-safe data released in 2022 from another lawsuit shows that between eight to ten million people, or 25 percent of responders reported reactions to Covid shots that were serious enough to require them to miss school, work or other normal activities or required medical attention or a hospital visit.

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Emails Reveal Fauci Ignored Early Reports Of Injuries Caused By COVID-19 Vaccine

Dr. Anthony Fauci knew COVID-19 vaccines were causing serious injuries within days of the vaccines’ rollout in December 2020, according to documents obtained by Children’s Health Defense (CHD). However, he didn’t respond to emails from people who described their injuries and asked for help — and he didn’t warn the public.

The 300-page tranche of documents released on April 21 relates to correspondence between the National Institutes of Health (NIH) and people who contacted the agency about adverse events they experienced after receiving the COVID-19 vaccine.

CHD requested the documents via a Freedom of Information Act (FOIA) request in November 2022. On April 12, 2023, CHD sued the NIH to obtain the records after the NIH failed to respond to the FOIA request.

As part of an October 2023 settlement, the NIH agreed to produce up to 7,500 pages of documents at a rate of 300 per month.

Dr. Joel Wallskog is a Wisconsin orthopedic surgeon who stopped practicing medicine after being injured by Moderna’s COVID-19 vaccine. He told The Defender the documents prove public health officials, including Fauci, “were well aware of the avalanche of adverse events that were occurring early in 2021.”

“No communication was made about these adverse events to the public,” said Wallskog, now co-chairman of React19, a nonprofit representing vaccine injury victims. “This prevented the public from receiving informed consent.”

Wallskog said that while the emails “are heartbreaking,” Fauci “was too busy to respond to Americans pleading for help.”

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