Eagle’s Eye Report: Big Pharma & Child Abuse

Eagle’s Eye Report: Big Pharma & Child Abuse


Eagle’s Eye Report: Big Pharma & Child Abuse (Archived)

90 Minute Special

Host: Roger Landry (TLB) – Co-Host & Producer: Stephen Roberts

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Intro by: Roger Landry (TLB)

Welcome again to Episode #9 of the Eagle’s Eye Report. Hosted by myself, Roger Landry (TLB), and Co-Hosted and Produced by my good friend and fellow patriot – Stephen Roberts. The title of today’s show is … Big Pharma & Child Abuse. The mission of this show is to be a mechanism for communicating the truth and facts in a country increasingly forbidding of these very concepts.

No, as I say weekly, this not a pleasant way to introduce a show … but today reality is blatant and not very pleasant in many aspects. Thus the reason, and intent behind the Eagle’s Eye Report.

Our mission is to keep you armed with the vital truth, as well as to present you with a platform where you can discuss these vital issues without fear of censorship or exclusion, that being the sponsor of this show … TLBTalk.com.

Now it’s down to business …

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Big Pharma & Child Abuse

If ever we are approached by danger or violence on just about any level, who is the first to be protected, to be hustled off to a safe area, or to be worried over with the utmost attention and focus? That would of-course be any children present, be they ours or not. For most normal adults this is very close to an instinctive action, being so close to automatic that it is difficult to even remember any forethought involved …

DANGER = PROTECT THE CHILDREN !!!

and for the most part (98% or better) we do! If a child is playing in the street and a car suddenly turns the corner and is bearing down on on them at a speed that leaves said child frozen in fear, a vast majority of adults would (almost) instinctively rush out into the street to push the child out of the path of the onrushing vehicle … even at the probable expense of their own safety or life. To any sane adult our children are the most precious asset, and the very future of, humanity, so to act in any other fashion is not really acceptable as a societal or a personal norm.

Yet today we will discuss an entity, mainly trusted by a very large portion of humanity, that not only totally disregards this premise … but specifically and knowingly puts our very youngest (babies) and toddlers in harms way as a matter of business and profit. Yes this is done knowingly and with foreknowledge by being the original source of the research clearly stating that these very actions are harmful and quite possibly even deadly to our babies/children.

No I am not exaggerating or pushing fear porn to make a personal point or to grandstand a situation that does not warrant it. As a matter of fact, if anything my pulpit is not high enough, nor is my bullhorn loud enough !!!

So let’s dig into this massive and unforgivable tyranny …

This episode is based on an article published by Dr. Mercola titled: Why Big Pharma Is Desperate to Get COVID Jab Into Babies. Yes that is the actual title and I’m sure you may now have a clearer understanding of why I chose this article to base this show on. As usual my commentary, opinion, and understandings are also a part of this presentation.

Let’s start this with a couple of slaps of reality:

Statistics show the rate of COVID associated hospitalization among children aged 5 to 11 is 0.0008%. Deaths are even more rare! In real-world terms, that’s so close to zero you basically cannot lower it any further. Yet, despite such reassuring data, children in this age group are urged to get two to three doses of the COVID jab, even though side effects of the injection could harm them for life, or kill them. In other words … it is a FACT that the supposed cure is far more dangerous to these children than the disease would ever be …

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As if the situation were not blatant enough already, June 15, 2022, the U.S. Food and Drug Administration’s vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — unanimously approved (21-0) to grant Emergency Use Authorization (EUA) to both Pfizer’s and Moderna’s COVID shots for infants and young children.

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Dr. Clare Craig, a diagnostic pathologist, points out that of the 4,526 children, aged 6 months to 4 years, who participated in Pfizer’s trial, 3,000 didn’t make it to the end of the trial. Why did two-thirds of the children drop out? Oftentimes, this happens when side effects are too severe for the participant to continue. Here, we don’t know why two-thirds of the participants were eliminated, and “on that basis alone, this trial should be deemed null and void …

••••

As noted by the Vaccine Safety Research Foundation, vaccinating infants and children who have no need for the shots and don’t benefit from them, just to “protect” adults, violates medical ethics. And since those who are jabbed still readily transmit the virus, the children are actually put at risk for no reason at all.

••••

Big Pharma needs this last remaining age group to be included (infants and toddlers) under the EUA, because once the emergency is finally declared ‘over,’ the next phase of liability shielding requires that the shots receive approval by the CDC’s Advisory Committee on Immunization Practices (ACIP).

Once the vaccine is on the childhood vaccination schedule, the vaccine makers are permanently shielded from liability for injuries and deaths that occur in ANY age group, including adults.

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So fasten your seat-belt and – Listen Up …

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Eagle’s Eye Report: Big Pharma & Child Abuse (Archived)

(Click on image below to listen to show)

SO BIG PHARMA WILL “KNOWINGLY” MAIM AND KILL OUR CHILDREN IN ORDER TO PROTECT THEIR PROFITS AND PREVENT CORPORATE LIABILITIES … OR … GENOCIDE ANYONE ???

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Show Talking Points from the following article:

The Reason Big Pharma Is Desperate to Get the Jab Into Babies

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Related article/video:

Dr. Rima Laibow – DEVASTATING! 90% of the Global Population Will Die – Globalist Agenda

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More Episodes of Eagle’s Eye Report (click on image below)

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About the Articles Author Roger Landry (TLB) spent about three decades of his adult life either in, or working for the military, with about two decades working directly for the Military Industrial Complex facilitating DOD contracts. His awakening to Political, Economic, and Health realities was about twelve short years ago. Since that time he has founded The Liberty Beacon Project (TLB) consisting of a half dozen proprietary global websites, media projects and partner websites across the planet. He contributes regularly to multiple forums both in and outside of TLB Project. Most of his work can be found on the TLB Flagship website TheLibertyBeacon.com

Image credit: Image of Joe Biden & Kamala Harris, In Public Domain – All other image credits on articles linked above.

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The Liberty Beacon Project is now expanding at a near exponential rate, and for this we are grateful and excited! But we must also be practical. For 7 years we have not asked for any donations, and have built this project with our own funds as we grew. We are now experiencing ever increasing growing pains due to the large number of websites and projects we represent. So we have just installed donation buttons on our websites and ask that you consider this when you visit them. Nothing is too small. We thank you for all your support and your considerations … (TLB)

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Disclaimer: TLB websites contain copyrighted material the use of which has not always been specifically authorized by the copyright owner. We are making such material available to our readers under the provisions of “fair use” in an effort to advance a better understanding of political, health, economic and social issues. The material on this site is distributed without profit to those who have expressed a prior interest in receiving it for research and educational purposes. If you wish to use copyrighted material for purposes other than “fair use” you must request permission from the copyright owner.

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The Massacre of the Innocents

The FDA and CDC launch a reckless nationwide medical experiment on children

I. The government is coming for your kids

Last week was shrouded in darkness. We saw the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) and the CDC’s Advisory Committee on Immunization Practices (ACIP) assemble the pieces of their Final Solution.

The meetings were surreal as so-called “experts” displayed no critical thinking skills and instead wallowed in clichés supplied to them by the pharmaceutical industry.

Over the course of five meetings in five days we witnessed crimes against humanity, the end of the bourgeoisie, and the likely end of America.

Let’s talk about what actually happened at the meetings, the short and long-term implications of the decisions that were made, and where we go from here.

II. The meetings themselves

The clinical trials of Moderna and Pfizer mRNA shots in kids all had the same flaws — enabled and encouraged by the permissive FDA. Moderna and Pfizer each:

1. Failed to demonstrate actual health benefits (so they relied on junk science “immunobridging” even though there are no valid correlates of protection);
2. Wiped out the control group, so there is no long term safety data; and
3. Caused catastrophic adverse events.

Contrary to their statutory obligations, the FDA/VRBPAC and CDC/ACIP do not act as regulators. Instead they see themselves as partners with Pharma. Indeed FDA and CDC officials often slip and say “we” when referring to the applicant — it’s all one big happy crime family.

At the meetings, the FDA and CDC went to great lengths to exaggerate the risks of Covid in children. As you know, there is no Covid-19 emergency in kids But Emergency Use Authorization requires a public health emergency so the FDA and CDC manufacture one.

Many presentations at the meetings last week cited the same British pre-print study that claims that Covid-19 was the 4th or 5th leading cause of death in children in the U.S. This is false.

Kelley Krohnert from Covid Georgia dismantles the pre-print.

The British academics who wrote the paper make two obvious errors. First they count deaths “with Covid” (tested after they got to the hospital for some other reason or underlying condition) as “from Covid.” If you remove the “with Covid” from the tally, the numbers shrink by about 35%.

The second major error in the pre-print is that the authors “compare the cumulative number of Covid deaths over 26 months to deaths from other causes over a one year period.” Whoops. So the FDA and CDC made their case by double-counting Covid-19 deaths in children.

Once these errors are corrected, Covid-19 drops down to the 8th or 9th leading cause of death. But as Ms. Krohnert explains:

Even given the corrected rankings above, there are also issues with the entire concept of showing the impact of Covid deaths in children using rankings. Rankings overstate the impact of Covid, because the top few causes of death far outweigh the causes further down the list. For example, in ages 1-4, accidents account for almost 25 times as many deaths as Covid-19 on an annualized basis. Furthermore, for each of the 4 age groups covered by the CDC slide, the very broad “accidents” is the leading cause of death. If we break that down further, causes of death like drownings, vehicle crashes, drug overdoses, would be individual causes of death greater than Covid in various age groups.

For those who want to argue, “if-it-even-prevents-one-death(TM)”: Covid-19 is NOT a vaccine-preventable-disease given that these shots do not stop infection, transmission, hospitalization, nor death. And given adverse events, Covid-19 shots will cause a net increase in deaths not a decrease.

If one really cares about the health of children, mandate fences around swimming pools, not experimental gene-modifying injections for the entire childhood population.

Ms. Krohnert contacted the authors of the paper to alert them to these errors and now they are revising the paper (a new draft is due next week). Of course, the FDA and CDC never admit that they were wrong because they don’t actually care about data.

At these meetings it is standard practice for FDA and CDC to lie about the benefits of these shots. Indeed the FDA went to great lengths to downplay the risk of vaccine-induced myocarditis in the briefing documents for Moderna and Pfizer. In preparing these documents the FDA relies on fixers — Matt Oster, Tom Shimabukuro, and John Su at CDC and Nicola Klein at Kaiser Permanente — to manipulate the data to fit the Pharma narrative.

However, one of the unusual things about the VRBPAC meeting on Tuesday is that Ruth Link-Gelles from CDC just straight up admitted that these shots have negative efficacy.

Then Tom Shimabukuro (citing his own slides and those from John Su and Nicola Klein) just straight up admitted that these shots cause myocarditis:

So I’m watching at home thinking… ‘no observed health benefits (that’s why they had to switch to immunobriding) and they are admitting that the shots have negative efficacy and cause myocarditis, therefore the risks outweigh the benefits. So how are they going to try to get out of this?’

And their argument is (supplied by Jacqueline Miller, Senior VP at Moderna) that the risk of myocarditis from Covid is greater than the risk of myocarditis from these shots. One of the obvious problems with that argument is that THESE SHOTS DO NOT PREVENT COVID. So the FDA is accepting a known risk from these shots in return for an imagined benefit that does not exist in the real world.

The VRBPAC and ACIP do not care about the facts at all. As George Lakoff famously observed, “facts bounce off of frames” and the frame that guides these public health zombies is, “vaccines are infallible.”

Adverse events. Others have done a better job of flagging adverse events in these clinical trials. Quant genius Jessica Rose wrote an excellent article about the harms in the Pfizer clinical trial and the Moderna clinical trial.

Look at pages 169 to 171 of the FDA briefing document for Moderna that showed 18 serious adverse events in the vaccine group as compared with only 1 in the placebo group in kids 6 through 23 months of age.

Furthermore, no one at the FDA/VRBPAC nor CDC/ACIP can explain why VAERS reports skyrocketed following the introduction of Covid-19 shots at the end of 2020 and why reports of vaccine injury in kids skyrocketed following the authorization of the Pfizer mRNA shot in kids last fall. Indeed FDA honcho Peter Marks had a meltdown at the end of the VRBPAC meeting on Wednesday because VAERS was trending on Twitter (apparently the public was not impressed with the VRBPAC’s self-serving nonsense).

Further observations:

At these meetings there is no critical thinking, no hard questions, and no debate.

There’s no science at all at these meetings, just a theatrical performance of science-y sounding things.

Quite literally, these so-called experts apologized to Moderna for asking them questions.

No one asks about adverse events.

There’s no discussion of antibody dependent enhancement, prion disease, or any of the other nightmare possibilities that seem to be emerging.

No VRBPAC member ever uses the phrase “negative efficacy” — even though the Pfizer application in kids showed negative efficacy between dose 1 and dose 2 and negative efficacy against the Omicron variant.

Antibodies are accepted as a valid measure even though everyone knows that there are no correlates of protection.

No one questioned the fact that FDA and CDC spent a year minimizing the risks of myocarditis and still could not get the safety signal to go away entirely.

No one questioned the fact that the international scientific consensus is that mRNA shots cause myocarditis in young people and that the U.S. is the only country in the world to push these shots on little kids.

The VRBPAC and ACIP members live in an alternative universe where sacrificing children is always acceptable to serve “The Greater Good(TM).”

VRBPAC and ACIP meetings are a horror movie come to life.

While these shots showed no benefit and catastrophic harms… the VRBPAC members wanted MORE, MORE, MORE!

Paul Offit led the charge on Tuesday by arguing that Moderna’s toxic shot should be a THREE dose series instead of the two doses that Moderna was applying for. Because VRBPAC members are selected for ideological conformity and groupthink, several other members piled on and echoed Offit’s call for MORE Moderna doses in kids.

On Wednesday, Offit again led the charge by arguing that Pfizer was “underdosed” (his word) at 3 mcg of mRNA in little kids and that they should have put MORE mRNA in there to produce a larger antibody response — adverse events in children be damned.

At this point, the bloodlust of these committees is unquenchable.

In the end, there was no need to even hold the meetings because the decisions were already made before they started.

On Tuesday, VRBPAC voted 21 to 1 to authorize the Moderna EUA application to inject mRNA into kids 6 to 17 years old. (There was 1 abstention — from the new guy, Bruce Gellin.)

On Wednesday, VRBPAC voted 21 to 0 to authorize the EUA applications to inject Moderna into kids 6 months to 5 years old and Pfizer into little kids 6 months to 4 years old.

On Saturday the CDC let it slip that Covid-19 shots in kids will be 10-dose vials. 10-dose vials are terrible because administration errors go up and because it’s impossible to guarantee consistency across doses (unless perfectly shaken before each dose, the ingredients may not be evenly distributed across the 10 doses). The federal government has paid billions of dollars to these companies up front for these shots. The fact that they did not require single dose vials shows that they do not know what they are doing and they have absolutely no concern for your health.

At the end of the meeting Saturday ACIP voted 12 to 0 to authorize the applications to inject Moderna and Pfizer into little kids.

Rochelle Walensky signed off on the Final Solution on Saturday night.

The federal government’s massacre of the innocents began Monday June 20, 2022.

III. The short and long-term implications of these decisions

The VRBPAC and ACIP believe that they achieved some sort of great victory. They got nostalgic at the end of the meeting as they looked back over the Final Solution that they had constructed over the last year. One can imagine Reinhard Heydrich and the other participants in the Wannsee Conference in 1942 felt the same way.

The reality is quite different. The FDA and CDC have guaranteed their own collapse.

Here’s how the next few years are likely to play out:

About one-third to half of the Democratic Party (including the overwhelming majority of the public health establishment) are afflicted with hypochondria, Stockholm Syndrome, and/or Munchausen Syndrome by Proxy. They are going to take their kids to be injected right away at any nearby CVS, Walgreens, or out of the back of a windowless van down by the river. They don’t care — “needles into arms (and legs)” is the only thing that Democrats believe in now. They’re junkies who get high from deadly virtue signaling.

Those poor kids are going to develop a wide range of adverse events — myocarditis, heart attacks, strokes, autoimmune disorders, cancer, endocrine disorders, infertility, and sudden “unexplained” death, to name a few. The over-boosted adults will suffer a similar fate. The bourgeoisie will lose their health, their dignity, and then all of their wealth to the Pharma cartel.

Over time, about half of injured families will come over to our side and become single issue medical freedom voters. That will give us the numbers we need to take power and prosecute the evil doers. All of the demographic advantages that Democrats thought would carry them to permanent majorities will evaporate.

Republicans, who understand vaccine injury better than Democrats at this point, will win the November midterm elections, the 2024 Presidential election, and the majority of local, state, and federal elections for the foreseeable future. Republicans will control all of the appropriations committees and oversight committees that have purview over HHS, FDA, CDC, and NIH. Fauci, Walensky, Califf, and Marks will all quickly retire to avoid being called to testify.

The meritocratic bourgeoisie system that has guided the U.S. for two centuries has already collapsed. It turns out that meritocracy was always a lie. Many of the most esteemed bourgeois institutions in the country were represented at the meetings last week — Stanford, Harvard, NEJM, and the Rockefeller Foundation — and they have no credibility now. When the fate of our nation was on the line they revealed themselves to be fascist clowns whose ideology renders them less smart than the average homeschooled fifth grader. The trust that was the lifeblood of our system is no more.

By failing to listen to the majority of the country that is deeply skeptical of these shots, the FDA and CDC deepened the polarization and made reconciliation nearly impossible.

These decisions will make no difference on the pandemic. If anything these authorizations of more shots for kids mean that the pandemic will continue for years — because the shots do not work and they fuel the evolution of variants that evade vaccines.

One might think that these decisions will lead to civil war or partition of the country into separate independent red and blue countries. At this point there is no need for red states like Texas and Florida to split off to form their own countries because Republicans are about to control EVERYTHING — Congress, the Presidency, and the Courts.

IV. Where do we go from here?

We’re all traumatized right now but we need to keep our head in the game. We need to become the leaders who will take over as things begin to fall apart.

The Advisory Committee on Immunization Practices is still going to vote on Thursday June 23, on Moderna’s EUA application to inject mRNA into kids 6 to 17. You can still register a formal comment — look for the blue comment button in the upper left hand corner or upload your own file.

Then, eight days from now the FDA is going to vote on the “Future Framework”. It’s a proposal to exempt Covid-19 vaccine manufacturers from clinical trials for reformulated shots. It’s literally the worst idea in the history of public health.

Long term we need to shift our strategy from lobbying others to taking power ourselves. Right now it seems the Republican Party is the best vehicle for accomplishing this goal. But honestly at this point, how many national Republican leaders (10? 20?) actually understand the enormity of the catastrophe that has been inflicted upon us over these past two years?

We need to make the point every chance that we get that the November midterm election is not about inflation, guns, abortion, drag shows, nor Ukraine. The 2022 midterm election is about stopping the Pharma genocide. Vote for politicians who publicly speak out against all of the following ongoing atrocities:

• Tony Fauci funded the creation of a gain-of-function virus that got loose and killed 6 million+ people.

• The medical establishment blocks access to safe and effective treatments in order to create the market for vaccines.

• Hospitals used and continue to use the wrong protocols because all of their financial incentives are not aligned with health.

• Poorly tested genetic experiments were injected into BILLIONS of people worldwide causing an increase in all-cause mortality and a wide range of horrific adverse events that are going to wreck human health and the economy for DECADES.

• Social media companies censor life saving information to protect the cartel while enriching themselves; the entire mainstream media is complicit in covering up the genocide.

• Schools and universities are incapable of conducting even basic risk benefit assessments and instead sacrifice the students in their care to the predatory pharmaceutical industry.

• The FDA and CDC sold the American people to the pharmaceutical industry.

THAT’S what needs to be addressed, unraveled, and prosecuted. Everything else is secondary.

Source

Another pile of dead vaxed people. They just keep piling up.

Another pile of dead vaxed people. They just keep piling up.

Jim Crenshaw – June 28th, 2022

If enough of these poor people pile up will that cause a wake up?
Source: JBossman008 on 153news.net

SourceSouth Australian Gov Criminal Organisation

The Reason Big Pharma Is Desperate to Get the Jab Into Babies

The Reason Big Pharma Is Desperate to Get the Jab Into Babies


Story at-a-glance

  • The rate of COVID-19 associated hospitalization among children aged 5 to 11 is just 0.0008%. In real-world terms, that’s so close to zero you basically cannot lower it any further

  • Despite that, the U.S. Food and Drug Administration’s vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — on June 15, 2022, unanimously approved to grant Emergency Use Authorization (EUA) to Pfizer’s and Moderna’s COVID shots for infants and young children

  • Pfizer’s EUA is for a three-dose regimen (3-microgram shots) for children 6 months to 5 years old; Moderna’s EUA is for a two-dose regimen (25-microgram shots) for children 6 months to 6 years

  • In granting this EUA, the FDA again ignored injury and death data and swept medical ethics aside

  • The drug companies need this last remaining age group to be included under the EUA, because once the emergency is finally declared “over,” the next phase of liability shielding requires that the shots receive approval by the CDC’s Advisory Committee on Immunization Practices (ACIP). Once the vaccine is on the childhood vaccination schedule, the vaccine makers are permanently shielded from liability for injuries and deaths that occur in any age group, including adults

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••••

Why Big Pharma Is Desperate to Get COVID Jab Into Babies

Analysis by Dr. Joseph Mercola

Statistics show the rate of COVID-19 associated hospitalization among children aged 5 to 11 is 0.0008%.1 In real-world terms, that’s so close to zero you basically cannot lower it any further. Yet, despite such reassuring data, children in this age group are urged to get two to three doses of the COVID jab, even though side effects of the injection could harm them for life, or kill them.

As noted by the Vaccine Safety Research Foundation in the video below, myocarditis — one of the recognized effects of the COVID jab — “has a mortality rate of 25% to 56% within three to 10 years, owing to progressive heart failure and sudden cardiac death.”

Sudden cardiac death is what the media and public health agencies are now glibly referring to as “sudden adult death syndrome” or SADS. The older and more appropriate description for SADS is “sudden arrhythmic death syndrome,” but they don’t even want to use the word “arrhythmic” anymore, as that tells you what the death is really caused by, and many are now aware that the jab can cause heart inflammation.

By avoiding the word “arrhythmic,” it’s easier for them to pretend as though people are dying for no apparent reason, and certainly not because of the COVID shots. Still, real-world facts tell us that SADS didn’t take off until after the shots were rolled out, and the vast majority of young healthy people who suddenly die for no apparent reason have been jabbed.2

Also, understand that if your child or you are injured by the shot, you cannot sue the drug company for damages and, so far, the U.S. government has rejected all but one of the claims filed with the Countermeasures Injury Compensation Program (CICP).3 At the current pace of about 18 claims a month, it would take 38 years just to get through the current backlog, Reuters has noted.4 Basically, many may die before their case even gets through review.

COVID Jab Authorization Granted for Babies

As if the situation were not bad enough already, June 15, 2022, the U.S. Food and Drug Administration’s vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — unanimously approved (21-0) to grant Emergency Use Authorization (EUA) to both Pfizer’s and Moderna’s COVID shots for infants and young children.5

Pfizer’s EUA is for a three-dose regimen (3-microgram shots) for children 6 months to 5 years old, while Moderna’s EUA is for a two-dose regimen (25-microgram shots) for children 6 months to 6 years.

In the video at the top of the page, Steve Kirsch, president of the Vaccine Safety Research Foundation, interviews reporter Toby Rogers, who endured the entire nine-hour day of the recent VRBPAC meeting.

The day before that meeting, June 14, Rogers published6 a written summary of Pfizer’s trial on young children, which he referred to as “an embarrassment.” “Any VRBPAC member who votes Aye on this junk science application should be removed from his/her job,” he wrote. Apparently, they all need to go.

In the interview, Rogers laments the fact that the VRBPAC members remain “locked in their information bubble” and won’t allow any conflicting data to influence their preconceived biases.

As noted by Rogers, they have a sacred duty to protect public health, and they’re being flippant about it. They’re ignoring data, they’re ignoring the pleas of the vaccine injured, they’re ignoring serious questions, they’re ignoring everything except the flimsiest bits and pieces upon which their narrative is built. Rogers called the experience “heartbreaking.”

VRBPAC Refuses to Answer Lawmakers’ Questions

The VRBPAC members aren’t even swayed by concerns from lawmakers. They simply ignore their questions too. As reported by The Defender:7

“The Vaccines and Related Biological Products Advisory Committee (VRBPAC) ignored pleas from experts, the vaccine injured and a congressman representing 17 other lawmakers to halt authorization until questions about the safety and efficacy of COVID-19 vaccines for the nation’s youngest children could be properly addressed …

Rep. Louie Gohmert (R-Texas) said there are many unanswered questions … ‘I’m deeply concerned that the push to vaccinate these children is nothing more than a dystopian experiment with unknown consequences,’ Gohmert told the committee. ‘Some of us have outlined these questions in a letter8 to VRBPAC but have not received any answers, and I pose some of them here.’ Gohmert said:

‘Number 1, why has the FDA refused to release the hundreds of thousands of pages of data from preapproval manufacturer studies, post-approval adverse events data and other post-approval manufacturer data?

Number 2, what is the cardiac risk factor in administrating these COVID vaccines to children?

Number 3, world-renowned immunologists have raised concerns about potential antibody-dependent enhancement, or ADE, resulting from COVID vaccines, and since ADE was a problem in prior unrelated respiratory vaccine trials, we need to know what studies, if any, the FDA has that it’s used regarding ADE from COVID vaccines in children 5 and under or any age group. Can the FDA affirm there’s no risk of ADE for vaccinated children?

Number 4, if widely approved among children 5 and under, how many lives, if any, does FDA estimate will be saved next year? Given the injuries reported in the FDA’s VAERS [Vaccine Adverse Event Reporting System] system, how will FDA evaluate serious vaccine injuries versus serious COVID outcomes?

Number 5, is it possible the proposed COVID vaccines in young children could create increased risk in future novel COVID variants?

Number 6, why has the FDA recently lowered the efficacy bar for COVID vaccines for youngest children? This change significantly lowers the expected benefits from any COVID vaccination for young children and it’s of particular concern given that over 70% of that age cohort already is seropositive.’

Gohmert said these questions and 13 other questions posed by lawmakers are critical and deserve answers from the FDA and VRBPAC prior to any EUA with the ‘accompanied protection for liability for all harm done.’”

Trial Showed COVID Jab Increases Infection Risk in Babies

In the video above, you can see Centers for Disease Control and Prevention director Dr. Rochelle Walensky, with a forced grin on her face, claiming “rigorous scientific review” has proven the shots to be safe and effective in infants and young children.

The video also features excerpts from a video in which Dr. Clare Craig, a diagnostic pathologist and “lover of data,”9 reviews what this “rigorous scientific review” actually found and what the FDA and CDC aren’t telling you. To hear Craig’s full summary of how Pfizer twisted its clinical data for young children, check out the video below.

Craig points out that of the 4,526 children, aged 6 months to 4 years, who participated in Pfizer’s trial, 3,000 didn’t make it to the end of the trial. Why did two-thirds of the children drop out? Oftentimes, this happens when side effects are too severe for the participant to continue. Here, we don’t know why two-thirds of the participants were eliminated, and “on that basis alone, this trial should be deemed null and void,” Craig says. Moreover:

Six of the children, aged 2 to 4 years, in the vaccinated group were diagnosed with “severe COVID,” compared to just one in the placebo group. So, what this actually shows is that the likelihood the shot is causing severe COVID is higher than the likelihood that it’s preventing it.

The only child who required hospitalization for COVID was also in the “vaccinated” group.

In the three weeks following the first dose, 34 of the children in the vaccinated group and 13 of the unvaccinated children were diagnosed with COVID. That means the children’s risk of developing symptoms of COVID within the first three weeks of the first dose actually increased by 30%. These data were ignored.

Between doses two and three, there was an eight-week gap, and the vaccinated arm again experienced higher rates of COVID. This too was ignored. After the third dose, incidence of COVID was again raised in the vaccine group, and this was ignored as well.

In the end, they only counted three cases of COVID in the vaccine arm and seven cases in the placebo group. They literally ignored 97% of all the COVID cases that occurred during the trial to conclude that the shots were “effective” in preventing COVID.

While they claim the triple-dose regimen reduced COVID, 12 of the children actually caught COVID twice in the two-month follow-up, and 11 of them were vaccinated.

The confidence interval for Pfizer’s jab is -370% at the lower end of the 95%, which suggests children who get the jab are nearly four times more likely of getting sick with COVID than their unvaccinated peers.10

Unscientific and Unethical Behavior

As reported by The Defender:11

“Combining all ages together, Pfizer said its three-dose regimen for children 6 months to 5 years old was 80% effective at preventing illness from the Omicron variant based on preliminary data from its clinical trial.

The 80% number was calculated 30 days after the third dose. As noted by committee members, the efficacy number is likely to go down after 30 days and post-approval monitoring was suggested.

Moderna said its two-shot vaccine was about 51% effective against infection from Omicron in children under 2, and about 37% among kids 2 to 5 years old, citing different efficacy numbers than what was reported by the company in March.

In a March 23 press release, Moderna said its vaccine in the 6-month to 2-year age group was only 43.7% effective. In the older age group, the company said its vaccine was 37.5% effective. A top official at Moderna has already said a booster will be necessary.”

As noted by the Vaccine Safety Research Foundation, vaccinating infants and children who have no need for the shots and don’t benefit from them, just to “protect” adults, violates medical ethics. And since those who are jabbed still readily transmit the virus, the children are actually put at risk for no reason at all.

It’s All About Securing Indemnification

So, how can we explain the irrational behavior of the FDA and CDC? Why don’t any of the data matter? Why doesn’t the science matter? Why don’t any of the red flags matter? And why are they handing out EUAs when the criteria for EUA are satisfied? Products must satisfy four criteria in order to get EUA:

  1. There must be an emergency
  2. A vaccine must be at least 30% to 50% effective
  3. The known and potential benefits of the product must outweigh the known and potential risks of the product
  4. There can be no adequate, approved and available alternative treatments (drugs or vaccines)

Unless all four criteria are met, EUA cannot be granted or maintained, yet here we are. COVID, by any reasonable measurement, is no longer an emergency, there are plenty of adequate alternative treatments, and the potential benefits in no way, shape or form outweigh the potential risks — especially not in infants and children under 5. That’s three out of four criteria that, clearly, are not met.

The short answer to the question, “Why are the CDC and FDA acting so irrationally?” is that both agencies are corrupt to the core and are no longer in the business of protecting public health. They are securing profits for the drug industry, and getting EUA for infants and young children is a crucial step toward securing permanent legal indemnity for the drugmakers.

As explained by Robert F. Kennedy Jr., in the short video clip above, they need this last remaining age group to be included under the EUA, because once the emergency is finally declared “over,” the next phase of liability shielding requires that the shots receive approval by the CDC’s Advisory Committee on Immunization Practices (ACIP).

This is the group that decides which vaccines are to be added to the childhood vaccination schedule. Once the vaccine is on the childhood vaccination schedule, the vaccine makers are permanently shielded from liability for injuries and deaths that occur in ANY age group, including adults.

The only way to break that indemnity is by proving the vaccine maker knew about the safety issues and withheld that information. You can learn more about this indemnification process in “The Real Reason They Want to Give COVID Jabs to Kids.”

So, the end goal is permanent immunity against liability for injury and death from the COVID shots in all age groups, and to get there, they first need the EUA to cover all children. After that, the ACIP approval becomes more or less a matter of rubber stamping. This is why they’re playing Russian roulette with the health of infants and young children.

Murder Has No Statute of Limitation

That said, if fraud can be proven, all indemnity falls by the wayside, and there’s no statute of limitation when it comes to murder, which some insist is what’s happening here.

The video above features “To The Lifeboats” podcaster Sam Dodson’s comments to the FDA VRBPAC during its open public hearing session to approve the COVID jabs for children between the ages of 6 months and 5 years. In a rapid-fire manner, he reviews several data points that ought to have put a halt to these injections, but didn’t; several instances where the FDA knew harm was occurring from these shots, or would occur, and they did nothing.

Another public comment was submitted by an as-yet unidentified individual. The submitted comment was provided to and reposted on Coquin de Chien’s Substack. Here are some select pieces:12

“This comment is NOTICE of possible criminal liability to Lauren K. Roth and members of the Vaccines and Related Biological Products Advisory Committee who owe duties of care, diligence, good faith, and loyalty in recommending ‘for’ or ‘against’ the EUA amendment for COVID-19 mRNA vaccine in children 6 months through 4 years of age.

Only two deaths are listed herein to establish knowledge. If the amendment is approved, it will have been done by committee members ‘knowing’ of felony crimes in context. Your investigation of these deaths should include death certificates, autopsy records, witness interviews, and immunization records.

Massachusetts Death Certificate 2022 SFN 5980 is a 7yo girl died January 18, 2022 listed as died from U071 ‘COVID-19,’ B49 ‘unspecified mycosis,’ J450 ‘predominantly allergic asthma,’ and R091 ‘pleurisy.’

VAERS_ID 2038120 is a 7yo girl in Massachusetts, who received her 2nd dose 1/13/2022 and was reported to VAERS 1/15/2022. PRIOR_VAX states, ‘Severe nausea and vomiting from 5 min post vaccination and for the next 8-10 hours.’

SYMPTOM_TEXT states, ‘Spiked a 103 fever, severe stomachache, has not had a bowel movement since the day before vaccination, which makes today 3 days without one. First vaccine caused severe nausea and vomiting from 5 minutes post injection and for the next 8-10 hours.’ This little girl suffered immeasurably 4 to 5 days as her intestines shut down due likely to impeded blood vessels servicing intestines.

Massachusetts Death Certificate 2021 SFN 56611 is a 48yo man died 11/16/2021 listed as died from U071 ‘COVID-19’ and E669 ‘OBESITY.’ SFN 56611 is known to have died less than 24 hours after inoculation.

In both cases, the Medical Examiners listed the cause of death as ‘COVID-19,’ when it was clearly not COVID-19. And in both cases, the Medical Examiners omitted listing causes Y590 ‘Viral vaccines’ and T881 ‘Other complications following immunization, not elsewhere classified,’ when these clearly were proximate and actual causes.

Death certificates from the state of Massachusetts are sent to the CDC, a federal entity. Thus, fraud on a state death certificate is a federal crime as it affects federal death records. Several federal felony crimes apply in this instance and are listed below.

If you dismiss this NOTICE and recommend the EUA amendment without first investigating these two deaths, you become liable for inchoate crimes and the felony crime of ‘misprision of felony.’ If a single person subsequently dies as a result of the amendment, all the elements will have been satisfied for you to face felony murder charges or involuntary manslaughter. Qualified immunity is not a valid defense …

There were found sixty likely C19 vaccine deaths in a 25-minute perusal of the 2021 and 2022 death certificates, which extrapolates to hundreds, probably thousands of C19 vaccine deaths in Massachusetts.

Refusal to investigate these fraudulent records is a crime that, because of the felony murder aspect, has no statute of limitations. Five, ten, or twenty years from now, if a federal prosecutor were to learn of this NOTICE, he or she would have significant evidence to bring charges for felony murder.

In summary, this NOTICE places you in a position requiring you to investigate these deaths prior to recommending the amendment. If you dismiss this NOTICE, you may be criminally liable for involuntary manslaughter, felony murder, and a list of federal crimes and inchoate crimes … Comment Tracking Number l4d-m52d-ge4m.”

Florida Bucks the Trend

My home state of Florida now stands out as the only U.S. state that is recommending AGAINST the COVID jab for 6-month-olds to 5-year-olds. Parents can still get their infants jabbed if they want, but the official state recommendation is not to do it, as there’s simply no scientific or logical rationale for doing so.

Florida also did not preorder any extra doses for this age group.13 In a June 18, 2022, Substack article, Dr. Robert Malone addressed the latest EUA authorization for infants and young children, and applauded Florida Gov. Ron DeSantis’ decision to buck the trend. It’s hard to believe he is the only governor in the U.S. who resisted this murderous threat to the children:14

“Have you looked at the VAERS data lately? The CDC apparently has not. In the USA alone, there have been 831,801 adverse events, of which 12,776 are life threatening. There have been 63,978 hospitalizations. There have been 13,293 deaths and 14,232 permanent disabilities from these vaccines.

True, these are ‘unverified’ — but previous research has shown that the VAERS system under-reported adverse events associated with vaccines, not over-reported … Then there are the international post-vaccine adverse event summaries.15

The CDC, under Freedom of Information Act Request (FOIA) has now admitted16 that even though they had promised to analyze the VAERS data before advising about these vaccines for children, they did not.

The VAERS data were NOT taken into consideration before the authorization of these genetic agents for babies and young children. Frankly, this is shocking. So shocking, it is hard for me to even write about it.

Now, approximately 430 children with other severe illnesses have died with COVID in the last 2.5 years (that would be 172 per year). Plus there have been 2,600 hospitalizations of children, most with underlying conditions — over that 2.5 year period. These numbers show that even before Omicron, in the case of children, COVID is less severe than flu …

Omicron in children is much less severe. We know this. The scientific evidence is clear. Yet the FDA goes back to data from the DELTA variant when discussing the effects of this virus … Governor DeSantis again has it right. It is time to stop. Parents must stop. The time is now to just say no.”

Last but not least, if you’re still unsure whether the COVID shot is the “right” choice for your child, please read through Dr. Byram Bridle’s “COVID-19 Vaccines and Children: A Scientist’s Guide for Parents,”17 published by the Canadian Covid Care Alliance. It goes through how the shots work, what the known side effects are, results from the clinical trial, the effects of the spike protein and much more.

••••

Sources and References:

••••

Stay tuned to …

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world orders review – June 25th, 2022

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https://www.bitchute.com/video/JRB1XlaYI1Jy/ [SHARE]
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SourceSouth Australian Gov Criminal Organisation

Monkeypox: Was COVID Just a Test Run? (Dr. David Martin Interview)

Monkeypox: Was COVID Just a Test Run? (Dr. David Martin Interview)

Man in America Published May 25, 2022

LIVE AT 10:30AM ET: Just as COVID starts to die out, a brand new public health threat emerges: Monkeypox! But luckily, Bill Gates and the W.H.O. already have it all planned out! Join me for a live interview with Dr. David Martin to discuss the latest global health scare, and what to expect next.

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SourceSouth Australian Gov Criminal Organisation

HAMMERED by Multiple ‘HEART ISSUES’ Caused by the Covid Vaccine (South Australia Reports)

TimsTruth Published June 16, 2022

My Rant about the Idiotic Medical Grubs

SourceSouth Australian Gov Criminal Organisation

This COVID shot will be available – NEVER!


‘These drugs will not be manufactured’

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