Editor’s Commentary: Most of the time, the details of a story are the most important parts. When we’re dealing with the death of a fellow American, it’s natural to want to know their name, situation, and the events that caused them to die. Today, I’m withholding the personal details at the request of the family, but I’m going to describe the situation nonetheless. It’s such an unfortunate scenario that it must be highlighted.
A 17-year-old girl contracted Covid-19 in August. She recovered easily, as the vast majority of young people who are infected by Covid-19 do. Severe or deadly Covid infections for people under the age of 20 are so rare, it makes headlines. This particular teen made it through Covid easily, recovering quickly and acquiring the natural immunity that is so effective at preventing future infections.
For some reason, she was vaccinated a few days later based on the anti-scientific recommendations of our government. As we’ve long said, there is no reason to inject experimental drugs into children, nor is there a reason to inject these drugs into those who have acquired natural immunity. The risks associated with the jabs far exceed the potential benefits of vaccinating kids or those with immunity. For a child who has immunity to get jabbed, as our government recommends, it absolutely asinine. There have been ZERO reported instances of anyone in the United States under the age of 20 dying from Covid after acquiring natural immunity.
Why was she forced to get vaxxed? Was it her school? Her job? Her parents? Her own choice based on the Big Pharma money-printing agenda being pushed by our government? As Megan Redshaw details below, she appears to have died from myocarditis complications, indicating it was the experimental drug inexplicably injected into her body that killed her.
Here’s Megan’s article. I had to highlight this one sad story because it angers me that Americans who have essentially zero risk of Covid are choosing or being forced to inject these experimental drugs into their bodies. This 17-year-old girl’s story should be a warning to any parent who thinks they’re doing right by their children to “protect” them from a disease that poses an infinitesimal risk to them. Here’s Megan…
VAERS COVID Vaccine Data Show Surge in Reports of Serious Injuries, as 5-Year-Olds Start Getting Shots
VAERS data released today by the CDC included a total of 875,653 reports of adverse events from all age groups following COVID vaccines, including 18,461 deaths and 135,400 serious injuries between Dec. 14, 2020, and Nov. 5, 2021.
The Centers for Disease Control and Prevention (CDC) released new data today showing a total of 875,653 adverse events following COVID vaccines were reported between Dec. 14, 2020, and Nov. 5, 2021, to the Vaccine Adverse Event Reporting System (VAERS). VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 18,461 reports of deaths — an increase of 383 over the previous week, and 135,400 reports of serious injuries, including deaths, during the same time period — up 7,943 compared with the previous week.
Excluding “foreign reports” to VAERS, 643,957 adverse events, including 8,456 deaths and 53,780 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Nov. 5, 2021.
Foreign reports are reports received by U.S. manufacturers from their foreign subsidiaries. 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 8,456 U.S. deaths reported as of Nov. 5, 10% occurred within 24 hours of vaccination, 15% occurred within 48 hours of vaccination and 26% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.
In the U.S., 427.6 million COVID vaccine doses had been administered as of Nov. 5. This includes: 250 million doses of Pfizer, 162 million doses of Moderna and 16 million doses of Johnson & Johnson (J&J).
Every Friday, VAERS publicizes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed. Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.
Numbers this week do not yet include reports from the authorization of Pfizer’s pediatric COVID vaccine for the 5 to 11 age group. Reports currently in VAERS for children under 12 are due to ”product administered to patient of inappropriate age.”
During a meeting on Oct. 26, by the U.S. Food and Drug Administration’s vaccine panel, Dr. Jessica Rose, a viral immunologist and biologist, said tens of thousands of reports have been submitted to the Vaccine Adverse Event Reporting System for children ages 0 to 18, and that 60 children have died — 23 of them were under 2 years old.
“It is disturbing to note that “product administered to patients of inappropriate age was filed 5,510 times in this age group,” Rose said. Two children were inappropriately injected, presumably by a trained medical professional, and subsequently died. This is malfeasance.”
This week’s U.S. data for 12- to 17-year-olds show:
- 22,782 total adverse events, including 1,400 rated as serious and 29 reported deaths. Two of the 29 deaths were suicides.
The most recent death includes a 17-year-old female from Washington (VAERS ID 1828901) who reportedly died Oct. 29 from a heart condition after receiving her second dose of Pfizer. According to the VAERS report, the girl had COVID in August and fully recovered. She received her first dose of Pfizer on Sept. 3 and her second dose on Sept 15.
On Oct. 23, she presented to the ER with chest pain and elevated troponin. She had an abnormal echocardiogram, abnormal EKG and became increasingly tachycardic. She then suffered cardiac arrest.
“Unfortunately she was not able to be resuscitated and died,” the report states. “Cause of death possible acute myocarditis.”
Other deaths include a 12-year-old girl from South Carolina (VAERS I.D. 1784945) who hemorrhaged 22 days after receiving Pfizer’s COVID vaccine, a 13-year-old girl from Maryland (VAERS I.D. 1815096) who died from a heart condition 15 days after receiving her first dose of Pfizer’s vaccine and a 17-year-old female from Texas (VAERS I.D. 1815295 who experienced an acute hyperglycemic crisis 33 days after being vaccinated.
- 59 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 96% of cases
attributed to Pfizer’s vaccine. - 552 reports of myocarditis and pericarditis (heart inflammation) with 542 cases attributed to Pfizer’s vaccine.
- 131 reports of blood clotting disorders, with all cases attributed to Pfizer.
This week’s U.S. VAERS data, from Dec. 14, 2020, to Nov. 5, 2021, for all age groups combined, show:
- 19% of deaths were related to cardiac disorders.
- 54% of those who died were male, 42% were female and the remaining death reports did not include gender of the deceased.
- The average age of death was 72.7.
- As of Nov. 5, 4,260 pregnant women reported adverse events related to COVID vaccines, including 1,337 reports of miscarriage or premature birth.
- Of the 3,123 cases of Bell’s Palsy reported, 51% were attributed to Pfizer vaccinations, 41% to Moderna and 8% to J&J.
- 723 reports of Guillain-Barré syndrome (GBS), with 41% of cases attributed to Pfizer, 30% to Moderna and 28% to J&J.
- 2,093 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
- 10,857 reports of blood clotting disorders. Of those, 4,790 reports were attributed to Pfizer, 3,864 reports to Moderna and 2,149 reports to J&J.
- 3,071 cases of myocarditis and pericarditis with 1,922 cases attributed to Pfizer, 1,016 cases to Moderna and 123 cases to J&J’s COVID vaccine.
Teen diagnosed with Guillain-Barré syndrome After COVID Vaccine
A 17-year-old girl was hospitalized for Guillain-Barré syndrome (GBS) — a rare disorder in which the body’s immune system attacks its nerves — after receiving a COVID vaccine. Shelby Allen said she’s thankful she isn’t paralyzed and didn’t die.
Shelby Allen, a 17-year-old from Dyer County, Tennessee, is hospitalized with a rare disorder in which the body’s immune system attacks its nerves. She developed the condition after getting a COVID vaccine.
SIGN UP #TheDefender: https://t.co/zL66Edfiw5https://t.co/M2wxPUxn3X
— Robert F. Kennedy Jr (@RobertKennedyJr) November 10, 2021
Allen started experiencing back pain and tingling in her arms after getting vaccinated. Symptoms progressed until she found herself unable to feel her arms and legs while bowling with her school’s team. Allen’s parents took her to the doctor in Jackson, Tennessee, where she was diagnosed with GBS and admitted to the ICU.
Allen’s doctor “knew right off the bat” her reaction was caused by a COVID vaccine, but still recommended people get vaccinated. Allen is hoping she’ll be able to walk by March for her high school graduation.
Taiwan temporarily halts second dose of Pfizer over myocarditis concerns
The Central Epidemic Command Center (CECC) said on Wednesday a panel of experts is suspending second doses of Pfizer-BioNTech’s COVID vaccine for children 12 to 17 years old amid concerns it may increase the risk of myocarditis.
Cases of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the outer lining of the heart) have been reported in children between 12 and 17 years old who received Pfizer’s vaccine.
CECC cited U.S. statistics which show the risk of experiencing heart inflammation after receiving a second dose is 10 times higher than after the first dose.
Chen Shih-chung, who heads up the CECC, said the Ministry of Health and Welfare’s Advisory Committee for Immunization Practices halted second doses of Pfizer for two weeks, during which time experts and CDC physicians will assess 16 cases of myocarditis among adolescents after Pfizer vaccination before making a decision on whether to go ahead with the second dose.
Hong Kong gives only a single dose to teens 12 to 17, while the UK recommends only one shot for children between ages 12 and 18.
More countries restrict Moderna vaccine over reports of myocarditis
France’s public health authority recommended people under 30 receive Pfizer’s COVID vaccine instead of Moderna, due to higher risks of heart problems in young adults, Reuters reported.
The Haute Autorite de Sante (HAS), an independent advisor to the French health sector, cited “very rare” risks linked to myocarditis, confirmed by a French study published Monday.
“Within the population aged under 30, this risk appears to be around five times lesser with Pfizer’s Comirnaty jab compared to Moderna’s Spikevax jab,” HAS said.
Germany’s advisory committee, known as STIKO, said on Wednesday people under age 30 should receive only Pfizer’s vaccine, as it causes fewer cases of heart inflammation in younger people. STIKO also recommended pregnant women receive only the Pfizer vaccine, regardless of their age.
The recommendations were based on new safety data from the Paul Ehrlich Institute — Germany’s authority in charge of vaccines, and new data.
The decision came after several other countries restricted the use of Moderna to older populations, including Canada, Finland, Denmark and Sweden. France’s medical regulator on Oct. 15 recommended using only Pfizer’s vaccine for booster shots, despite the European Union’s drug regulator last month approving Moderna’s booster for all age groups over 18.
Pfizer asks FDA to authorize third booster dose for all people 18 and older
As The Defender reported Nov. 10, Pfizer and BioNTech on Tuesday asked the FDA to authorize a third dose of their COVID vaccine for all people 18 and older, even though advisory panels to the FDA and CDC in September overwhelmingly rejected a similar request.
The companies said their new request is based on the results of a study, conducted by Pfizer and BioNTech, which has not been published or peer-reviewed. The companies said the study of more than 10,000 volunteers showed vaccine efficacy against symptomatic infection of 95% or greater for people receiving the booster.
Pfizer did not disclose how many participants experienced asymptomatic infection, or whether the clinical trial — as did Pfizer’s clinical trial for 5 to 11 years olds — included individuals with natural immunity acquired from previous SARS-CoV-2 infection.
Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.
© 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
They’re Trying to Shut Us Down
Over the last several months, I’ve lost count of how many times the powers-that-be have tried to shut us down. They’ve sent hackers at us, forcing us to take extreme measures on web security. They sent attorneys after us, but thankfully we’re not easily intimidated by baseless accusations or threats. They’ve even gone so far as to make physical threats. Those can actually be a bit worrisome but Remington has me covered.
For us to continue to deliver the truth that Americans need to read and hear, we ask you, our amazing audience, for financial assistance. We just launched a GiveSendGo page to help us pay the bills. It’s brand new so don’t be discouraged by the lack of donations there. It’s a funny reality that the fewer the donations that have been made, the less likely people are willing to donate to it. One would think this is counterintuitive, but sometimes people are skeptical because they think that perhaps there’s a reason others haven’t been donating. In our situation, we’re just getting started so please don’t be shy if you have the means to help.
Thank you and God bless!
JD Rucker
Sin leads to death and choosing to believe lies is the root of sin.
There is no reason to inject anyone with this dangerous, deadly, and ineffective experimental drug. Whether the efficacy is 0%, 100%, or somewhere in between. If it worked, then everyone who chose not to take it made their own choice, assuming the risk on themselves. Since it doesn’t work, it’s irrelevant.
Nobody has the right or the authority, short of God Himself, to make a decision for someone else wherein there is significant risk of serious injury or death in either path chosen. That is a person’s own decision to make, weighing the risks for themselves, or in the case of children, the parent’s decision.
May God severely judge those who’ve pressured, coerced, pushed, and forced others into taking this dangerous drug. May He take from them 100 fold that which they took from others. May He harshly remind them, in a manner they will ever again forget, that they have no right, and no authority to encroach on His domain!
They volunteered. Little sympathy. It is sad.
Not necessarily. In contract law when information is purposefully and blatantly withheld or suppressed, the contract is not made in good faith and is therefore basically void. At that point its no differrent than volunteering for a tetanus shot and having the doctor amputate a limb instead. You volunteered for one thing and got something else. The question is did her parents know and understand the risks, and if not why.