Vaxx Update: The competing narratives here between the official "safe and effective" and the ever greater real-world evidence of "death and severe injury" from the C-19 "vaccine" rollout is stunning!
Our thanks to Gabi for referring some of today's news stories...
The CDC now recommends COVID shots for babies and toddlers.
Learn what parents won’t be told before the shot.
COVID-19 shots for kids starting at 6 months have FDA authorization and CDC recommendation.
The White House is ready to start getting “shots in arms” of our babies and toddlers this Tuesday, June 20, 2022, mere days after the federal agencies fulfilled their part in the Biden administration’s plan to vaccinate America.
Now that FDA has authorized the Pfizer and Moderna COVID shots as of Friday, June 17 and the CDC gave its recommendation on Saturday, June 18, there are over 18 million more children (ages 6 months through 5 years) who will now be strategically targeted (keep reading for evidence) for the shots.
States were able to pre-order COVID shots for kids under 5 at the beginning of June, two weeks before the FDA even met publicly to discuss their recommendation. There are 10 million doses at the ready for Tuesday the 20th, with more on the way.
Parents must question the COVID shots.
The White House knows that people are going to turn to trusted people they know, like a pediatrician or a community leader, to make this decision. So they have already started educating “a network of providers and trusted messengers.”
The White House is working with the American Academy of Pediatrics to create a speakers’ bureau to spread its messaging. The CDC site is ready to go with social media downloads with the tagline “less worry, more play” if infants and toddlers get the shot.
On June 8 the White House made it clear that their messages will be coming from every direction:
“We’re going to be reaching out to millions of children and their parents and guardians nationwide through WIC and SNAP, through Head Start and child care programs, through HUD-supported housing, and Medicaid, and CHIP.
“We’re going to work with trusted organizations like the American Academy of Pediatrics, the Association of Children’s Museums, the American Library Association, the National PTA, the National Diaper Bank Network, and the National Association of Community Health Centers, as well as a number of Black, Latino, AANHPI, and Native American community-based organizations.
“We’re also going to activate our 17,000-plus-member HHS COVID-19 Community Corps, which will help provide creative, kid-focused English and Spanish toolkits to trusted local messengers.
“At this point in the Biden administration’s vaccination program, our partners are accustomed to this process, and so are we.
“As we have said previously, we are not in the predicting business; we’re in the planning business.”
–Excerpts from White House Press Briefing on the Administration’s Operational Plan for Vaccinating Children Under 5 Against COVID-19.[i]
Friends, it’s our responsibility to use our voices. Let’s talk to pregnant moms, bring up the topic with neighbors, and have difficult conversations with family members. But always remember to open the door with love and curiosity.
Please click on this graphic for a link to the article…
Breaking: 58 babies who received mRNA COVID-19 vaccines suffered life-threatening adverse events
An analysis of VAERS reports shows that contrary to the FDA's briefing document claiming that the majority of adverse events in Pfizers' clinical trial were non-serious – at least 58 cases of life-threatening side effects in infants under 3 years old who received mRNA vaccines were reported.
For some, it is unclear if they survived.
It is also unclear why the infants were vaccinated, and whether they were part of the clinical trials.
However, in the upcoming FDA meeting on Wednesday, the FDA will not be able to argue it did not know.
While the FDA is preparing to approve the mRNA COVID-19 vaccine for infants and toddlers aged 6 months to four years, and claims in its' VRBPAC Briefing Document released today that the majority of adverse events found in Pfizers' trial were non-serious - Real-Time magazine analysis reveals at least 58 life-threatening adverse events in infants and toddlers aged under 3 years old reported to VAERS.
The most common serious adverse events were life-threatening bleeding, anaphylactic shock, anticholinergic syndrome, encephalitis, hypoglycemia, and neuroleptic syndrome. In most of the reported cases, these are multi-system injuries.
In some cases it is not clear what happened to the babies - did they survive? And if so, have they recovered?
Most reports do not specify under what circumstances the infants were vaccinated, and if they participated in the clinical trials.
While the FDA claims in its' briefing document that the vaccine efficacy in infants is 80.4%, the document reveals that the claim is based on a total of 10 symptomatic cases of COVID-19 identified in the trial among 1415 participants – 7 of them in the placebo group vs. 3 in the vaccine group.
Please click on this photo for a link to the article…
Cases of Brain Damage in Children Skyrocket Following COVID-19 Vaccines
First published on June 22, 2022
Weakened hearts, blood clots, and now you can add neurological brain damage to the list of side effects being reported in children following COVID-19 vaccinations.
In at least one case, one poor child developed all three conditions.
In a case study published earlier this month (May 2022) in the Journal of Neuroimmunology, a 15-year-old girl developed encephalopathy, myocarditis, and thrombocytopenia simultaneously following the second dose of the Pfizer COVID-19 vaccine.
As billions of people are getting vaccinated, it is not surprising that vaccine-related adverse events are coming into focus and being reported in the scientific literature.
Here we report a case of COVID-19 mRNA Pfizer- BioNTech vaccine-associated encephalopathy, myocarditis, and thrombocytopenia following the second dose of vaccine which responded dramatically to methylprednisolone. (Source.)
Neurological issues are common side effects of all childhood vaccines, and are often grouped under the label of “autism.” There is a very clear correlation between increased vaccinations of children to rising rates of autism in the United States, even though the U.S. Government health agencies refuse to acknowledge any causal effect between the bloated childhood vaccine schedule and diagnoses of autism.
It is no surprise, therefore, that we are seeing similar reports following the deadly COVID-19 vaccines.
But how do reports of brain damage following COVID-19 vaccines compare to the rate of brain damage reported with all other vaccines administered for the previous 30 years before the roll-out of the COVID-19 experimental shots?
To develop a baseline, I chose to search VAERS (Vaccine Adverse Events Reporting System) for all cases reporting “encephalopathy” following vaccination.
“Encephalopathy” is a term for “any diffuse disease of the brain that alters brain function or structure.” (Source.)
This term alone does not represent all the cases of neurological damage to the brain that are reported in VAERS, but it does give us a point of reference to compare cases reported after COVID-19 shots as compared to all other FDA-approved vaccines for the previous 30+ years.
And what I found was that there is a 2,000%+ increase in brain injuries being reported after COVID-19 shots.
Here are the results based on a search for “encephalopathy” symptoms after COVID-19 vaccines. (Source.) Notice the high rate of death among these cases of “encephalopathy.”
Please click on this photo for a link to the article…
If every doctor in America took just five minutes to review the latest VAERS report, they would quickly realize that the Covid “vaccines” are extremely toxic, injurious, and often fatal.
Hence, any physician who participates in such a risky and dangerous experiment is administering a poisonous injection to their trusting patients, thereby profoundly violating their quite sacred Hippocratic Oath.
Submitted by The Covid Coach
SOTN Exclusive
All of the following COVID-19 ‘vaccine’ data and information comes directly from the U.S. Federal Government’s Vaccine Adverse Event Reporting System (VAERS).
The Vaccine Adverse Event Reporting System (VAERS) is a United States program for vaccine safety, co-managed by the U.S. Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA).[1]
VAERS is a postmarketing surveillance program, collecting information about adverse events (possible harmful side effects) that occur after administration of vaccines to ascertain whether the risk–benefit ratio is high enough to justify continued use of any particular vaccine.
VAERS, the Vaccine Safety Datalink, and the Clinical Immunization Safety Assessment (CISA) Network are tools by which the CDC and FDA monitor vaccine safety[2] to fulfill their duty as regulatory agencies charged with protecting the public.(Source: Vaccine Adverse Event Reporting System)
Please click on this graphic for a link to the article…
Here, let the data speak for itself; here’s the PDF of the actual report:
Documents show Pfizer's COVID-19 vaccine causes autoimmune disease and VAED
The Pfizer documents that the Food and Drug Administration (FDA) was forced to publish by court order revealed that the Big Pharma company knew that its COVID-19 vaccine is causing autoimmune disease and vaccine-associated enhanced disease (VAED).
But the FDA chose to ignore it.
The Pfizer vaccine uses mRNA technology, which was never authorized before December 2020 for human use – and for a reason.
During animal trials for SARS and MERS viruses, it had the opposite of its intended effect and worsened the disease by inducing antibody-dependent enhancements.
Eighteen months after the injections were administrated in trials, all the animals died.
Yet somehow, the vaccine was granted emergency use authorization around the world and administered to millions to protect them against a disease that statistically kills only less than 0.2 percent of those affected, the majority being the elderly, the vulnerable, and those who already had existing underlying conditions. Even then, the vaccine failed. (Related: Pfizer, FDA knew their COVID vaccine causes immunosuppression, ADE, VAED.)
An example is Australia. In June, nearly 90 percent of Australia is considered fully vaccinated, but the country is still riding its largest wave of COVID-19 deaths since March.
According to data, at least 4 in 5 of the COVID-19 deaths recorded were among the fully vaccinated.
This suggests that the COVID-19 injections don't work.
Moreover, it suggests that the injections make the recipients more vulnerable to infection.
Data revealed that all of the deaths could have been avoided if the FDA bothered to read the documents submitted by Pfizer. Instead, the FDA attempted to delay the release of the company's vaccine safety data for 75 years, despite approving the injection after only 108 days of safety review.
Please click on this photo for a link to the article…