This is a real gem by Harrison Smith at the American Journal.  It's always tricky to take a DEADLY SERIOUS issue and put it into some humorous form.  One of the most amazing things about humor is the fact that you can often simply tell the truth because the truth is often plenty absurd all by itself.  Here, Harrison lays out exactly how these deadly experimental vaccines were rolled out and how badly we were lied to about them, lies that morphed from one to another until they jabbed hundreds of millions of trusting/coerced people.

by Kyle Becker
TrendingPolitics.com

The Wall Street Journal unleashed an editorial over Independence Day weekend that is a devastating takedown of the rush to get all toddlers jabbed with Covid vaccines and boosters.

“In fact, we don’t know if the vaccines are safe and effective,” Allyssia Finley wrote in a WSJ editorial. “The rushed FDA action was based on extremely weak evidence. It’s one thing to show regulatory flexibility during an emergency. But for children, Covid isn’t an emergency. The FDA bent its standards to an unusual degree and brushed aside troubling evidence that warrants more investigation.”

“While adult Covid vaccines clearly met this standard in late 2020, the toddler vaccines don’t,” Finley added.

“Only 209 kids between 6 months and 4 years old have died from Covid—about 0.02% of all virus deaths in the U.S.,” the editorial adds. “About half as many toddlers were hospitalized with Covid between October 2020 and September 2021 as were hospitalized with the flu during the previous winter. More children were hospitalized during the Omicron wave last winter, but hospitalization rates were still roughly in line with the 2019-20 flu season. None of the 5,400 or so toddlers in Moderna’s trial were hospitalized for Covid. Yet at least 15 were hospitalized for non-Covid infections.”

TheGatewayPundit.com

According to a recent ruling by an Uruguayan judge, the government and the pharmaceutical company Pfizer must provide all the information they have on the COVID vaccine’s biochemical composition, including any evidence of “graphene oxide” or “nanotechnological elements,” as well as proof of the vaccine’s efficacy and safety.

Administrative Litigation Court (TCA) Judge Alejandro Recarey made the order in response to a request to suspend the immunization of children from 5 years of age in Uruguay.

By Julian Conradson
TheGatewayPundit.com

On Sunday, Moderna’s Chief Medical Officer Dr. Paul Burton announced the vaccine maker had officially kicked off phase 1 “human trials” for its new two-in-one Flu-Covid jab.

According to Burton, who spoke exclusively with 9News Australia, phase one clinical trials for the hybrid vaccine are currently underway and progressing on schedule, with the new treatment expected to be rolled out between late 2023 and early 2024.

By Julian Conradson
TheGatewayPundit.com

According to a newly released study by the University of Oxford, a jaw-dropping 94% of recently approved medications are not supported by high-quality evidence that demonstrates their benefits. What’s more, just like with the experimental Covid-19 ‘vaccines,’ side effects and adverse reactions to these drugs are being severely underreported across the board.

When looking at medical drugs that have been approved since 2008 under the Cochrane reviews – a “leading” international journal and database that is endorsed by over 100 organizations worldwide, including the US Food and Drug Administration (FDA) -researchers determined that just 87 of the 1,567 medications (6%) had clinical data that met the “high-quality” standard.

By Jordan Schachtel
TheDossier

The August 23, 2021 FDA approval of Pfizer’s Comirnaty vaccine was a cause for celebration. Marked as a turning point in the battle against COVID19, the announcement was highly publicized by the Biden Administration with the clear intention to extinguish “vaccine hesitancy” and boost uptake.

President Biden says anyone who was waiting for an FDA-approved Covid vaccine should "go get your vaccination and get it today" https://t.co/UrDwnjMZGc pic.twitter.com/OQ4Uwet23M

— CNN Breaking News (@cnnbrk) August 23, 2021

TheGatewayPundit.com

America’s Frontline doctors are speaking out about FDA’s approval of Remdesivir for the treatment of COVID-19 in babies.  They are beyond shocked.

The FDA recently reported that they had approved Remdesivir for the ‘treatment’ of COVID-19 in babies.

America’s Frontline doctors can’t believe what they are seeing.

A UK company literally named "Venomtech" announced a massive venom peptide and venom fragment library to be used for drug discovery by pharmaceutical companies (as well as pesticide used for agricultural companies). They write: "...[we are] helping our customers worldwide make pioneering advances in drug discovery, crop protection, and cosmetics. We have the largest library of naturally sourced venom-derived compounds in the UK, from a growing collection of vertebrate and invertebrate species." The use of snake venom in pharmaceuticals isn't a "conspiracy theory." It's a common practice, representing what most bioscience experts would describe as the cutting edge of drug discovery.
 

Dr. Bryan Ardis uncovers alarming new information that points to another possible culprit . . . venom poisoning. Most people have no idea that snake venom is an ingredient that is BIG with BIG PHARMA.

This nearly hour-long conversation between Stew Peters and Dr. Bryan Ardis exposed a new COVID-related topic that is raising eyebrows everywhere. Essentially, after realizing how odd it was that antivenom medicines like monoclonal antibodies were effectively treating Covid, Dr. Ardis began questioning the narrative that what we are calling COVID originated from a bat in a Chinese wet market. “Is Covid a venom, and this is why they don’t want you using monoclonal antibodies?” Dr. Ardis asked.

To answer this question, Dr. Ardis sought out establishment media “fact-checkers” to see if they were attempting to discredit any claims that the source of Covid-19 was a snake and not a bat. A quick internet search reveals plenty of mainstream media publications admitting at the onset of the Covid outbreak that it may have been derived from snakes. “Every time the snake is mentioned, fact-checkers 1,2,3,4,5,6 constantly fact-check it and spin it to the bats. There is no fact-checking about bats. They keep letting you look at bats,” Dr. Ardis said.

The doctor also claimed that Chinese scientists dismissed the bat theory at the beginning of the Covid outbreak because the type of bats the virus allegedly came from were hibernating at the time. He also said genetic sequence testing done on sick patients in Wuhan found their genetic sequence matched two snakes, the Chinese Krait and King Cobra, not bats.

New unredacted trove of documents reveal ADE cases were documented by Pfizer and the FDA but they tried concealing those shocking figures for decades.

The Food and Drug Administration (FDA) has released another batch of internal Pfizer documents under court order showing even more evidence that Pfizer and the FDA knew of the antibody dependent enhancement (ADE) phenomenon and tried to cover it up.

The trove of 11,000+ pages of documents, released on April 1, reveal both agencies knew that vaccine-induced ADE was occurring and worked to cover it up by claiming “no new safety issues have been raised.”

The next batch of Pfizer vaccine documents from the FDA has been produced (11,043 pages), as well as an unredacted version of the post-marketing experience report, available at https://t.co/BzkKyrnK5U or https://t.co/vT3d5OMGlC

— Aaron Siri (@AaronSiriSG) April 1, 2022

ADE occurs after the mRNA vaccine primes the immune system for a potentially deadly overreaction.