FLASHBACK: Fauci Talks About the Possibility of Vaccine Enhancing the Disease and Making People Worse in March 2020

ADE (antibody-dependent enhancement) is one of the most catastrophic risks of any mass-vaccination campaign.

Several prominent scientists have warned about the potential of the COVID-19 injections resulting in the development of ADE.

As Dr. Robert Malone warned, ADE is the worst case scenario of the experimental vaccination rollout.

Given the waning protection of the COVID-19 jabs, the worst case scenario includes the virus replicating more efficiently than it would without a vaccine.

This scenario causes antibodies to enhance virus entry and replication in cells.

That’s ADE and a significant challenge to vaccine development.

If the experimental injection fails to prevent transmission and your antibody response enhances the infection, it’s a recipe for disaster.

That’s what is potentially developing with the COVID-19 jabs.

Although there weren’t any COVID-19 jabs available in 2020, the United States saw more COVID-19 deaths in 2021.

U.S. COVID-19 deaths reach 800,000; 2021 was worse than 2020https://t.co/wDvs2cj3dd

— CP24 (@CP24) December 12, 2021

It’s clear the experimental injections aren’t doing the job Big Pharma and public health officials said they would.

There were multiple warnings about the possibility of ADE, but the red flags went ignored by federal agencies and the mainstream media.

MARCH ‘21 NIH WARNED VAX TRIAL OF ADE & WORSE OUTCOMES WHEN EXPOSED TO SARS COV2 !!! Informed consent disclosure to vaccine trial subjects of risk of COVID-19 vaccines worsening clinical disease – PubMed https://t.co/EJcxtd2sDU

— Leanna (@leannaevolution) August 14, 2021

People are not ‘anti-vaxxers’ for reading beyond MSM & asking legitimate Qs 👉
“COVID-19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated“ – PubMed
#ADE https://t.co/U6AW9ZLteU

— BumblingAlong (@ChickensAndBeez) September 21, 2021

As noted in the study titled “Informed consent disclosure to vaccine trial subjects of risk of COVID-19 vaccines worsening clinical disease”

Results of the study: COVID-19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern: that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralising antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID-19 disease via antibody-dependent enhancement (ADE). This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID-19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials.

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Conclusions drawn from the study and clinical implications: The specific and significant COVID-19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.

This study clearly states the COVID-19 jabs may worsen the disease and informed consent of ADE is critical.

Does the CDC mention the possibility of ADE?

Let’s see what their website says about potential side effects:

COVID-19 vaccination will help protect people from getting COVID-19. Adults and children may have some side effects from the vaccine, which are normal signs that their body is building protection. These side effects may affect their ability to do daily activities, but they should go away in a few days. Some people have no side effects, and allergic reactions are rare.

Serious side effects that could cause a long-term health problem are extremely unlikely following any vaccination, including COVID-19 vaccination. Vaccine monitoring has historically shown that side effects generally happen within six weeks of receiving a vaccine dose. For this reason, the U.S. Food and Drug Administration (FDA) collected data on each of the authorized COVID-19 vaccines for a minimum of two months (eight weeks) after the final dose. CDC is continuing to monitor the safety of COVID-19 vaccines even now that the vaccines are in use.