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FEDERAL LAWSUIT SEEKS IMMEDIATE HALT OF COVID VACCINES, CITES WHISTLEBLOWER
TESTIMONY CLAIMING CDC IS UNDER-COUNTING VACCINE DEATHS

By Megan Redshaw
Global Research, July 21, 2021
Children's Health Defense 20 July 2021
Region: USA
Theme: Law and Justice, Media Disinformation, Science and Medicine

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***

America’s Frontline Doctors filed a motion to stop the use of Emergency Use
Authorization (EUA) COVID vaccines for anyone under 18, anyone with natural
immunity or anyone who hasn’t received informed consent.

America’s Frontline Doctors (AFLDS) filed a motion July 19, seeking immediate
injunctive relief in Alabama Federal District Court to stop the use of Emergency
Use Authorization (EUA) COVID vaccines — Pfizer/BioNTech, Moderna and Johnson &
Johnson (J&J) — for three groups of Americans.

According to a press release, AFLDS is asking to immediately stop administration
of experimentalCOVID vaccines in anyone 18 and younger, all those who have
recovered from COVID and acquired natural immunity, and every other American who
has not received informed consent as defined by federal law.

The 67-page motion requests the judge issue a preliminary injunction pursuant to
§ 360bbb–3(b)(1)(C) for the following reasons:

 * There is no emergency, which is a prerequisite to issuing EUA and EUA
   renewals for COVID vaccines.
 * There is “no serious or life-threatening disease or condition.”
 * Vaccines do not diagnose, treat or prevent SARS-CoV-2 or COVID.
 * Known and potential risks of the vaccine outweigh their known and potential
   benefits.
 * There are adequate, approved and available alternatives to vaccines.
 * Healthcare professionals and vaccine candidates are not adequately informed.

The authors of the motion attached a declaration by a whistleblower who came
forward alleging deaths occurring within 72 hours of receiving a COVID vaccine
are significantly under-reported in the Centers for Disease Control and
Prevention’s (CDC) Vaccine Adverse Events Reporting System (VAERS) maintained by
the U.S. Food and Drug Administration (FDA).

As of July 9, reported deaths in the VAERS totaled 10,991. Of those, 4,593
occurred within 72-hours of vaccination.

The whistleblower — a computer programmer who developed more than 100 distinct
healthcare fraud algorithms, and who has expertise in healthcare data analytics
that allows her to access Medicare and Medicaid data obtained by the Centers for
Medicare and Medicaid Systems (CMS) — filed a sworn statement under penalty of
perjury alleging the actual number of COVID vaccine-related deaths is closer to
45,000.

As Health Officials, Media Ramp Up Vaccine Coercion, They Scapegoat the
Unvaccinated

The whistleblower alleged that VAERS, while extremely useful, is under-reported
by a conservative factor of at least five.

In her statement, she said:

“On July 9, 2021, there were 9,048 deaths reported in VAERS. I verified these
numbers by collating all of the data from VAERS myself, not relying on a third
party to report them. In tandem, I queried data from CMS medical claims with
regard to vaccines and patient deaths, and have assessed that the deaths
occurring within 3 days of vaccination are higher than those reported in VAERS
by a factor of at least 5. This would indicate the true number of
vaccine-related deaths was at least 45,000. Put in perspective, the swine flu
vaccine was taken off the market which only resulted in 53 deaths.”

AFLDS said the findings were shocking, and informed consent is impossible when
safety data is not accurate.

In a press release, AFLDS said:

“It is unlawful and unconstitutional to administer experimental agents to
individuals who cannot make an informed decision as to the true benefits and
risks to the vaccine on an independent basis. They must be of an age or a
capacity to make informed decisions and have been provided with all of the
risk/benefit information necessary to make an informed decision.”

One of the named plaintiffs, Deborah Sobczak, the mother of a 15- and
17-year-old, said in the press release:

“My child will not be the subject of an experiment. What kind of monsters are we
allowing to control us? Perfectly healthy children have developed heart
inflammation, brain bleeding and even died! I have had enough. I am not
sacrificing my child so a pharmaceutical company can experiment on her. This
madness has to stop.”

There is no emergency warranting EUA of COVID vaccines, plaintiffs allege

According to the complaint, the U.S. Department of Health and Human Services
(HHS) secretary, named as one of the defendants in the lawsuit, declared on Feb.
4, 2020, pursuant to § 360bbb–3(b)(1)(C), that SARS-CoV-2 created a “public
health emergency.”

This initial emergency declaration has been renewed repeatedly and remains in
force today — a necessary legal prerequisite for the issuance of vaccine EUAs,
the complaint states. EUA allowed the mass use of the vaccines by the American
public before the completion of the standard regimen of clinical trials and FDA
approval.

Plaintiffs allege the emergency declaration and its multiple renewals are
illegal because there is no underlying emergency. Using HHS COVID death data,
SARS CoV-2 has an overall survivability rate of 99.8% globally, which increases
to 99.97% for persons under the age of 70. This is consistent with the seasonal
flu, the complaint states.

Plaintiffs argue HHS deliberately inflated COVID case data

Plaintiffs allege HHS’ data is deliberately inflated. On March 24, 2020, HHS
changed the rules applicable to coroners and others responsible for producing
death certificates and making “cause of death” determinations exclusively for
COVID.

The rule change states: “COVID-19 should be reported on the death certificate
for all decedents where the disease caused or is assumed to have caused or
contributed to death.”

According to the complaint, HHS statistics showed 95% of deaths classified as
“COVID-19 deaths” involved an average of four additional comorbidities.
Plaintiffs claim the CDC knew the rules for coding and selection of the
underlying cause of death would result in COVID being the underlying cause more
often than not.

Plaintiffs said the actual number of COVID cases is also far lower than the
reported number due to emergency use of polymerase chain reaction (PCR) tests,
which are used as a diagnostic tool for COVID. The PCR tests are themselves
experimental products, authorized by the FDA under separate EUAs. The package
inserts state PCR tests should not be used to diagnose COVID.

The complaint alleges the way in which the PCR tests are being administered
knowingly guarantees an unacceptably high number of false positive results.

COVID vaccine risks undisclosed and under-reported, lawsuit says 

AFLDS medico-legal researchers analyzed the accumulated COVID vaccine risk data
and found migration of the pathogenic SARS-CoV-2 spike protein in the body. Yet
vaccines were authorized without any studies demonstrating where the spike
proteins traveled in the body following vaccination, how long they remain active
and what effect they have, the complaint states.

AFLDS researchers analyzed VAERS and discovered an increased risk of death from
COVID vaccines. The database indicated vaccine deaths in the first quarter of
2021 represented a 12,000% to 25,000% increase in vaccine deaths, year-on-year.

From 2009 to 2019, there were 1529 reported deaths associated with all vaccines
reported to VAERS, according to the motion. In the first quarter of 2021, there
were more than 4,000 reported deaths with 99% of all reported vaccine deaths in
2021 attributed to the COVID vaccine. Only 1% were attributed to other vaccines
in the system.

Plaintiffs also disclosed evidence of reproductive harm, vascular disease,
autoimmune disease, neurological damage and they highlighted an increased risk
of harm for children with COVID vaccines to support their position.

Why the secrecy around V-Safe data?

The complaint called attention to the secrecy of the CDC’s V-Safe system — a
parallel system used to track reported adverse events via a smartphone app
controlled exclusively by the CDC.

Plaintiffs raised concerns that information in V-Safe exceeds that in VAERS.
They claim VAERS is inaccurate because it potentially includes fewer than 1% of
all vaccine adverse events, and the federal government is failing to provide
data from other monitoring sources such as V-Safe, CMS and the military.

Plaintiffs stated informed consent cannot be given without understanding the
risks. They said they can’t help but wonder why HHS would fail to disclose to
the public critical information related to risk from it’s reporting systems,
“particularly in light of the fact that they have had the time and resources to
study and extend the authorizations on the vaccines, build an enormous vaccine
marketing machine and roll out vaccine clinics all over the nation.”

The lawsuit was filed by several law firms, including RENZ Law. The complaint
and whistleblower declaration can be read here.

*

Note to readers: Please click the share buttons above or below. Follow us on
Instagram, @crg_globalresearch. Forward this article to your email lists.
Crosspost on your blog site, internet forums. etc.

Megan Redshaw is a freelance reporter for The Defender. She has a background in
political science, a law degree and extensive training in natural health.

Featured image is from CHD

The original source of this article is Children's Health Defense
Copyright © Megan Redshaw, Children's Health Defense, 2021

--------------------------------------------------------------------------------

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Articles by: Megan Redshaw


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