CDC Approves COVID Vaccines for Youngest Kids + More | By The Defender Staff | ChildrensHealthDefense.org

The Defender’s COVID NewsWatch provides a roundup of the latest headlines related to the SARS CoV-2 virus, including its origins and COVID vaccines.

Miss a day, miss a lot. Subscribe to The Defender’s Top News of the DayIt’s free.

CDC Approves COVID Vaccines for Youngest Kids

NBC News reported:

On Saturday, the Centers for Disease Control and Prevention Director Dr. Rochelle Walensky signed off on COVID vaccines for the youngest Americans. Her endorsement means shots can begin immediately, finally ending the two-and-a-half-year wait on the part of parents of children under 5.

Walenksy accepted the recommendation within hours after the CDC advisory committee voted unanimously in favor of the Pfizer-BioNTech and Moderna vaccines for children as young as 6 months.

A Centers for Disease Control and Prevention advisory committee on Saturday endorsed Pfizer-BioNTech and Moderna’s COVID-19 vaccines for the youngest children, the last step before CDC Director Dr. Rochelle Walensky could issue her final sign-off.

The unanimous recommendations from the CDC’s Advisory Committee on Immunization Practices followed the Food and Drug Administration’s authorization of the shots on Friday.

White House Health Official Makes False Claim About COVID Vaccines

The Epoch Times reported:

Continue on Source: CDC Approves COVID Vaccines for Youngest Kids + More

Pfizer Classified Almost All Severe Adverse Events During COVID Vaccine Trials ‘Not Related to Shots’ | By Michael Nevradakis, Ph.D. | the Defender | ChildrensHealthDefense.org

The case reports included in Pfizer clinical trial documents, released June 1 by the U.S. Food and Drug Administration, reveal a trend of classifying almost all adverse events — and in particular severe adverse events — as being “not related” to the vaccine.

Miss a day, miss a lot. Subscribe to The Defender’s Top News of the DayIt’s free.

The latest release by the U.S. Food and Drug Administration (FDA) of Pfizer-BioNTech COVID-19 vaccine documents reveals numerous instances of participants who sustained severe adverse events during Phase 3 trials. Some of these participants withdrew from the trials, some were dropped and some died.

The 80,000-page document cache includes an extensive set of Case Report Forms (CRFs) from Pfizer Phase 3 trials conducted at various locations in the U.S., in addition to other documentation pertaining to participants in Pfizer-BioNTech vaccine trials in the U.S. and worldwide.

The FDA on June 1 released the documents, which pertain to the Emergency Use Authorization (EUA) of the vaccine, as part of a court-ordered disclosure schedule stemming from an expedited Freedom of Information Act (FOIA) request filed in August 2021.

Public Health and Medical Professionals for Transparency (PHMPT), a group of doctors and public health professionals, submitted the FOIA request.

CRFs show deaths, severe reactions to the vaccines during Phase 3 trials

The CRFs included in this month’s documents contain often vague explanations of the specific symptoms experienced by the trial participants.

They also reveal a trend of classifying almost all adverse events — and in particular severe adverse events (SAEs) — as being “not related” to the vaccine.

For example:

  • A female in her early 50s (randomization number 86545) who participated in the trial at the Sterling Research Group in Cincinnati, Ohio, died of an apparent myocardial infarction on Nov. 4, 2020. She had received two doses of the vaccine, on Sept. 10 and Sept. 29, 2020.

The patient had a medical history of chronic obstructive pulmonary disease, hypertension, hypothyroidism, osteoarthritis of the knees and attention deficit disorder. Her death was listed as “not related” to the vaccine, and was instead attributed to “hypertensive cardiovascular disease.”

  • A female in her late 50s (randomization number 220496), who participated in the trial at Cincinnati Children’s Hospital Medical Center, died of cardiac arrest on Oct. 21, 2020. Her death, however, was indicated as “not related” to her vaccinations (which occurred on July 30, 2020, and Aug. 20, 2020) as it “occurred 2 months after last receipt of study agent,” according to her CRF.

The participant’s medical history included obesity, placement of a gastric sleeve, gastroesophageal reflux, sleep apnea, supraventricular tachycardia, hypothyroidism, depression and asthma.

Continued on Source: Pfizer Classified Almost All Severe Adverse Events During COVID Vaccine Trials ‘Not Related to Shots’

CDC Admits It Never Monitored VAERS for COVID Vaccine Safety Signals | By Josh Guetzkow, Ph.D. | the Defender | ChildrensHealthDefense.org

In response to a Freedom of Information Request submitted by Children’s Health Defense, the Centers for Disease Control and Prevention last week admitted it never analyzed the Vaccine Adverse Event Reporting System for safety signals for COVID-19 vaccines.

Miss a day, miss a lot. Subscribe to The Defender’s Top News of the DayIt’s free.

In a stunning development, the Centers for Disease Control and Prevention (CDC) last week admitted — despite assurances to the contrary — the agency never analyzed the Vaccine Adverse Event Reporting System (VAERS) for safety signals for COVID-19 vaccines.

The admission was revealed in response to a Freedom of Information Act (FOIA) request submitted by Children’s Health Defense (CHD).

In September 2021, I published an article in The Defender in which I used the CDC’s published methodology to analyze VAERS for safety signals from COVID-19 vaccines.

The signals were loud and clear, leading me to wonder “why is nobody listening?”

Instead, I should have asked, “Is anybody even looking for them?”

After that article was published, I urged CHD’s legal team to submit a FOIA request to the CDC about its VAERS monitoring activities.

Since CDC officials stated publicly that “COVID-19 vaccine safety monitoring is the most robust in U.S. history,” I had assumed that at the very least, CDC officials were monitoring VAERS using the methods they described in a briefing document posted on the CDC website in January 2021 (and updated in February 2022, with minor changes).

I was wrong.

Continued on Source: CDC Admits It Never Monitored VAERS for COVID Vaccine Safety Signals

The FLCCC Protocol for COVID-19 Jab Injuries | Analysis by Dr. Joseph Mercola | Fact Checked

STORY AT-A-GLANCE

  • COVID-19 is clearly no longer an emergency. The real emergency now is the continued use of the COVID “vaccines,” because they’re creating injuries on a level that is truly alarming and unprecedented. VAERS data reveal the COVID jabs have caused more harm in 18 months than all other vaccines on the market, combined, over the past three decades
  • Raw data from the Pfizer trial also show the shots were associated with an increased risk for death from the start, and both Pfizer and the FDA knew it
  • Data also show highly “vaccinated” and boosted nations are now experiencing record case and death rates from COVID compared to countries with low injection rates
  • We’re now finding the COVID shots have negative efficacy, meaning, if you have received the shot and are exposed to COVID, you are more likely to get sick, not less likely, compared to someone who is unvaccinated
  • The Frontline COVID-19 Critical Care Alliance (FLCCC) has developed a protocol for those injured by the COVID jabs called I-RECOVER, which you can download from covid19criticalcare.com in several different languages

In the “Tea Time” episode above, Drs. Pierre Kory and Paul Marik review the Frontline COVID-19 Critical Care Alliance (FLCCC) protocol for those injured by the COVID jabs. They also discuss what’s in the shots, their lack of safety and efficacy, adverse events, and the controversial issue of “shedding.”

Kory and Marik are both part of the FLCCC, which was founded in 2020 to share early treatment protocols for COVID-19. Kory is an ICU specialist, triple board certified in internal medicine, critical care and pulmonary medicine. He now runs a private tele-health practice specializing in the treatment of COVID-19, so-called “long-COVID” and vaccine injuries.

Marik is one of the most-published ICU specialists in the world, and best known for his vitamin C protocol for sepsis. The FLCCC’s protocol for COVID is known as the MATH+ protocol, which has undergone multiple revisions over the course of the pandemic.

Now, as injuries from the COVID jab are stacking up, they’ve also added a post-vaccine treatment called I-RECOVER,1 which you can download from covid19criticalcare.com in several different languages.

Continue reading on Source: The FLCCC Protocol for COVID-19 Jab Injuries

Fauci Tests Positive for COVID After 4 Doses, Gets Grilled at Senate Hearing on Response to Pandemic | By Megan Redshaw | the Defender | ChildrensHealthDefense.org | 6-16-22

Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, tested positive for COVID-19, his office said Wednesday. Fauci, who is quadruple-vaxxed, was experiencing “mild symptoms.”

By Megan Redshaw

Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases (NIAID) and chief medical advisor to President Biden, tested positive for COVID-19, his office said Wednesday.

The NIAID said Fauci, 81, tested positive for the virus through a rapid antigen test and is currently “experiencing mild symptoms.”

“Dr. Fauci will isolate and continue to work from his home,” the statement said. “Dr. Fauci will follow the COVID-19 guidelines of the Centers for Disease Control and Prevention [CDC] and medical advice from his physician and return to the NIH [National Institutes of Health] when he tests negative.”

This is the first time Fauci, who is quadruple-vaxxed against COVID-19, has announced he’s tested positive for the virus.

The NIAID confirmed Fauci received four COVID-19 vaccine doses, including two boosters.

Despite testing positive, Fauci today testified remotely during a hearing before the Senate Committee on Health, Education, Labor and Pensions, where he was grilled about the federal response to the pandemic.

“Our current vaccines have maintained their effectiveness for preventing severe COVID-19,” Fauci said, referring to the Omicron variant during his opening statement. “Individuals who have received only their primary vaccine regimen have a greater likelihood of getting infected with the Omicron variant than with previous variants.”

“Importantly, booster shots have been shown to significantly reconstitute and enhance the level of antibodies that neutralize the Omicron variant and in sub-lineages,” he added.

In May 2021, in an interview on MSNBC, Fauci said people who got vaccinated would not get infected.

Continued on Source: Fauci Tests Positive for COVID After 4 Doses, Gets Grilled at Senate Hearing on Response to Pandemic

Judy Mikovits Shocks The World: Most Damning Covid Evidence Bombshell The World Has Seen | Stew Peters Network | Rumble.com | 6-15-22

Science and medicine have no other modern definition than FAKE at this point in time. Dr. Judy Mikovits presents her findings of medical fraud, and how Fauci was involved in her arrest AND career destruction.

Buy tickets to see Mikovits at the crimes against humanity conference: https://pathtotruth.ticketleap.com/t/Stewpeters/

Watch this new segment NOW at StewPeters.com!

Source: Judy Mikovits Shocks The World: Most Damning Covid Evidence Bombshell The World Has Seen

FDA: Vaccines and Related Biological Products Advisory Committee (VRBPAC) – June 14th and 15th Meetings – CHD TV: Livestreaming Video & Audio | ChildrensHealthDefense.org

VRBPAC Meeting: June 15th

The FDA VRBPAC will be convening on the topic of amending the Moderna COVID-19 mRNA vaccine EUA to allow it’s use in the 6 through 17 years age group, as well as the 6 month through 5 years age group. The Pfizer-BioNtech COVID-19 mRNA vaccine will also be considered in amending it’s EUA to include use among infants and children 6 months through 4 years old.

Dr. Meryl Nass will provide live-blogging of the event.

More info on these meetings can be found Here

In Case You Missed It:

The People’s Testaments: The Infertility Files — Part 1: Rachel Williams’ Story

Recommended Clips

Dr. Patrick Flynn on ‘Infertility: A Diabolical Agenda’

‘I’ve Never Had a Single Unvaccinated Patient with Autism’ — Dr. Ben Tapper 

CHD TV – Censorship Free. Guaranteed.

You Make It Possible

Children’s Health Defense depends on generous donations from our community. Large or small, every donation gets us closer to achieving our goals.

Listen to what RFK, Jr. has to say.

Become a Member | Donate Now

Listen to what RFK, Jr. has to say.

Become a Member | Donate Now

Children’s Health Defense
852 Franklin Ave., Suite 511
Franklin Lakes, New Jersey 07417
Contact us

Grand Jury Day 8 – Closing Arguments: Dr. Reiner Fuellmich | English | Odysee.com

Closing Arguments: Dr. Reiner Fuellmich – Attorney at Law, Germany

Grand Jury Day 8 – Closing arguments

A group of intern. attorneys and a judge are conducting a criminal investigation modeled on the grand jury proceedings to present to the public all available evidence of past crimes against humanity related to Covid-19 of the “leaders, organizers, instigators, and accomplices” who assisted in the formulation and execution of a common plan for a pandemic. This investigation is of the people, by the people, and for the people, so YOU can be part of the jury.

By presenting a complete picture of the factual situation, including the geopolitical and historical background, the trial aims to raise awareness of the collapse of the current hijacked system and its institutions.

Livestream links & more:
https://grand-jury.net

Source: Grand Jury Day 8 – Closing Arguments: Dr. Reiner Fuellmich | English

From Dr. Fuellmich’s Telegram channel: https://t.me/ReinerFuellmichEnglish/375

Reiner Fuellmich 🇺🇸/🇬🇧/🇦🇺, [6/13/2022 8:29 AM]
[Forwarded from Corona Investigative Committee 🇺🇸/🇬🇧/🇦🇺]
[ Photo ]
All closing arguments as single cut
Grand Jury Investigation, Day 8

Follow the link:
➥ to the closing argument of Dr. Reiner Fuellmich, Germany

(https://odysee.com/@GrandJury:f/Grand-Jury-Day-8-Fuellmich-Odyssee:9)➥ to the closing argument of Dipali Ohjha, India

(https://odysee.com/@GrandJury:f/Grand-Jury-Day-8-Ojha-Odyssee:1)➥ on the closing argument of Dexter L-J Ryneveldt, South Africa

(https://odysee.com/@GrandJury:f/Grand-Jury-Day-8-Ryneveldt-Odyssee:6)➥ on the closing argument of Virginie De Araujo-Recchia, France

(https://odysee.com/@GrandJury:f/Grand-Jury-Day-8-Recchia-Odyssee:5)➥ on the closing argument of Michael Swinwood, Canada

(https://odysee.com/@GrandJury:f/Grand-Jury-Day-8-Swinwood-Odyssee:d)➥ on the closing argument of Ana Garner, USA

(https://odysee.com/@GrandJury:f/Grand-Jury-Day-8-Garner-Odyssee:4)➥ on the closing argument of Leslie Manookian, USA

(https://odysee.com/@GrandJury:f/Grand-Jury-Day-8-Manookian-Odyssee:2)⚠️ ➥ to the vote (https://t.me/CoronaInvestigativeCommittee/84)⚠️

Website and all sessions: Grand-Jury.net

Keep up to date:
@CoronaInvestigativeCommittee

182 New Reports of Deaths After COVID Vaccines, CDC Data Show | by The Defender Staff | Children’s Health Defense 

VAERS data released Friday by the Centers for Disease Control and Prevention show 1,295,329 reports of adverse events from all age groups following COVID-19 vaccines, including 28,714 deaths and 236,767 serious injuries between Dec. 14, 2020, and June 3, 2022.

Miss a day, miss a lot. Subscribe to The Defender’s Top News of the DayIt’s free.

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,295,329 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and June 3, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 7,734 adverse events over the previous week.

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 28,714 reports of deaths — an increase of 182 over the previous week — and 236,767 serious injuries, including deaths, during the same time period — up 1,726 compared with the previous week.

Of the 28,714 reported deaths, 18,638 cases are attributed to Pfizer’s COVID-19 vaccine, 7,524 cases to Moderna and 2,483 cases to Johnson & Johnson (J&J).

Excluding “foreign reports” to VAERS, 829,329 adverse events, including 13,225 deaths and 83,801 serious injuries, were reported in the U.S. between Dec. 14, 2020, and June 3, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 13,225 U.S. deaths reported as of June 3, 16% occurred within 24 hours of vaccination, 20% occurred within 48 hours of vaccination and 59% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 588 million COVID-19 vaccine doses had been administered as of June 3, including 347 million doses of Pfizer, 222 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).

Continued on Source: 182 New Reports of Deaths After COVID Vaccines, CDC Data Show

Horrific Discovery In Warmed Jab Vials: There’s A Reason The Bioweapon Must Be Stored At -70 Degrees | Stew Peters & Dr. Jane Ruby | Stew Peters Network | Rumble.com

The vaccines are frozen to keep the PARASITES from growing! Dr. Jane Ruby has found SHOCKING discoveries on the truth of what is ACTUALLY in these vaccines! Watch this new segment NOW at StewPeters.co

Source: Horrific Discovery In Warmed Jab Vials: There’s A Reason The Bioweapon Must Be Stored At -70 Degrees