Vaxx Update: The adverse effects evidence keeps piling-up and Big Pharma and Government are way slow to admit any serious issues. And now they've "approved" the Vaxx injections for young children?

The sleight-of-hand and insanity continue... read all about it.

Thank you, Gabi, for this story…

Simply revolting, however, I am neither surprised nor disappointed. Just looking around, the fraud and moral “dry rot” in our society has reached a severe level - very few things are as they seem. Buyer beware on EVERYTHING. I find a lot of folks half-crazed.

The sad thing is many of these ‘celebrity’ and high-profile phonies have touted others to take a CLEARLY and LEGALLY experimental vaccine… with truly unknown long-term, and likely very bad, outcomes for many.

More than 2200 European celebrities, elites and politicians caught falsely registered as vaxxed against COVID-19

If it’s happening across Europe, it is happening here in America also. Guaranteed!

More “good for thee but not for me” bullshit. If it has been going on here in the U.S., it might likely be considered a federal crime. How many of our so-called ‘elites’ have been out pushing the VAxx on people in a false and misleading way? How many have done it for money?

I have heard about MASSIVE back-end ‘capitation fees’ and bonuses paid to medical groups and clinics for total Vaxx shots delivered. Will those ever be disclosed?

It raises some very interesting and complex legal questions.

Under the FDA’s EUA releasing the various COVID-19 “vaccines” for early use, there is NO legal liability for downstream ill effects. HOWEVER, if intentional “fraud” can be be established that MAY remove the liability shield.

I highly suspect there will be MASSIVE class action lawsuits in the near future if the ongoing Vaxx adverse effects and SADS death rates continue to climb unabated.

Folks will rightfully want revenge and compensation. TBD…

Please click on this image for a link to the video… (4:56)

FDA Approves Pfizer's COVID-19 Vaccine for Young Children

On June 12, 2022, the U.S. Food and Drug Administration (FDA) released a long-awaited analysis of the Pfizer Inc. (PFE) and BioNTech SE (BNTX) COVID-19 vaccine for potential use in children under age 5.

The analysis suggested that the vaccine appears to be safe and effective in preventing the illness in children in that age group. No new safety concerns were present in the evaluation.

The FDA's post about Pfizer's vaccine follows a similar posting that the FDA made earlier about Moderna's vaccine for children under 6.3 The FDA is scheduled to meet on June 15 to determine whether to approve shots from either or both companies.

The shots would be administered to many of the nation’s 18 million children beneath age 5, which includes babies, toddlers and preschoolers.

Please click on this image for a link to the article…

Again, this next image is courtesy of Gabi.

Are you beginning to see the UTTER INSANITY of all this? This is a direct quote from a Voting Member of the FDA’s Review Panel deciding to approve the Vaxx program for younger children….

U.S. FDA panel weighs COVID vaccines for children as young as 6 months

June 15 (Reuters) - Advisers to the U.S Food and Drug Administration on Wednesday will vote on whether to recommend authorization of two COVID-19 vaccines for the millions of children ages five years and under, an important step toward immunizing a group that has not been eligible for the shots during the pandemic.

The U.S. government is planning for a June 21 start to its under-5 vaccination campaign should the vaccines from Moderna Inc (MRNA.O) and Pfizer (PFE.N)/BioNTech (22UAy.DE) receive FDA authorization, White House COVID-19 response coordinator Ashish Jha said last week.

FDA finally admits that COVID-19 vaccines can cause blood clots

The U.S. Food and Drug Administration (FDA) has altered its guidance for the Wuhan coronavirus (Covid-19) "vaccine" from Janssen (Johnson & Johnson), which the federal agency now admits causes blood clots.

An FDA news release explains that the Janssen injection now has limited authorized use in individuals 18 years of age and older due to the risk of thrombosis with thrombocytopenia syndrome (TTS), "a syndrome of rare and potentially life-threatening blood clots in combination with low levels of blood platelets with onset of symptoms approximately one to two weeks following administration."

In other words, after a person gets injected with Janssen, potentially life-threatening blood clots could develop in a time period as short as one week.

Even so, the FDA claims that the Janssen shot's "benefits" outweigh the risks, and that people should still line up to get it.

The "Fact Sheet for Healthcare Providers Administering Vaccine" now reflects the FDA's authorized use revision for Janssen. It includes a warning at the beginning summarizing the risk of TTS, as well as a revision concerning the risk of blood clots with low levels of blood platelets added to the "Fact Sheet for Recipients and Caregivers."

"We recognize that the Janssen COVID-19 Vaccine still has a role in the current pandemic response in the United States and across the global community," said Peter Marks, director of the FDA's Center for Biologics Evaluation and Research. "Our action reflects our updated analysis of the risk of TTS following administration of this vaccine and limits the use of the vaccine to certain individuals."

Both FDA and CDC knew about heart risks but pushed covid shots anyway

Please click on the image for a link to the article…

Another suggestion from Gabi. Here is Steve Kirsch’s “take” on the FDA VAxx approval process. Steve is a fellow Substack Newsletter Editor. I HIGHLY recommend his material.

Concise summary of the FDA meeting (Day 1): Went as expected; unanimous approval

For those of you who haven't had time to watch the whole thing: unanimous vote to approve the Moderna vaccine EUA 6 to 11 and 12 - 17. Tomorrow is Moderna 6 month to 5 year; Pfizer 6 mo to 4 yrs.

Please click on this image for a direct link to Steve’s article…