Regardless of what’s behind recent outbreaks of white lung disease, some medical experts said they believe public health officials are downplaying environmental stressors and ignoring the immune-degrading effects of vaccination and poor diets that make people — and especially children — more vulnerable to infections of all kinds.

ChildrensHealthDefense.org

Media outlets and some mainstream medical experts are sounding the alarm over reports of pediatric white lung disease (or syndrome) outbreaks. But not all medical experts agree on what’s causing the outbreaks or what they mean — or whether the condition even exists.

Many, including experts interviewed by The Defender, do agree on this, however: Regardless of what the disease is and what’s behind the recent outbreaks, public health officials are downplaying environmental stressors and ignoring the immune-degrading effects of vaccination and poor diets that make people — and especially children — more vulnerable to infections of all kinds.

Pediatricians Dr. Paul Thomas and Dr. Larry Palevsky on a recent episode of “Good Morning CHD” on CHD.TV pushed back on media claims of white lung disease, instead pointing to vaccine-induced hyperimmunity and often-dismissed environmental factors.

TheGatewayPundit.com

The Florida Surgeon General, Dr. Joseph A. Ladapo, is demanding answers from Dr. Robert M. Califf, the Commissioner of the U.S. Food and Drug Administration (FDA), regarding the detection of host cell DNA fragments in mRNA COVID-19 vaccines developed by Pfizer and Moderna.

The Florida Surgeon General sent a letter to FDA Commissioner Califf and CDC Director Mandy Cohen on December 6, pressing for greater transparency about the potential for DNA integration into the human genome—a concern that could have far-reaching implications.

The Florida Public Health Integrity Committee discussed these issues on November 14, 2023, and Ladapo urged the FDA to consider their findings. In addition, he reminded Califf of a previous communication dated May 10, 2023, which had yet to receive a response.

On May 10, Ladapo sent a letter to Califf and former CDC Director Rochelle Walensky regarding the risks of the experimental COVID-19 vaccines

Brownstone.org

When everyone from the President to your primary care doctor declared loudly and wholeheartedly in December 2020 that the newly FDA-authorized Covid mRNA vaccines were “safe and effective” – what were those claims based on?

In this article, I will review the contractual and regulatory framework applied by the US government to the initial development, manufacture, and acquisition of the Covid mRNA shots. I will use the BioNTech/Pfizer agreements to illustrate the process.

The analysis will show that:

• The Covid mRNA vaccines were acquired and authorized through mechanisms designed to rush medical countermeasures to the military during emergencies involving weapons of mass destruction.

• These mechanisms did not require the application of, or adherence to, any laws or regulations related to vaccine development or manufacturing.

• The FDA’s Emergency Use Authorization for the vaccines was based on clinical trials and manufacturing processes conducted with no binding legal standards, no legally proscribed safety oversight or regulation, and no legal redress from the manufacturer for potential harms. (This last point is being challenged in multiple court cases, so far to no avail.)

A federal district court judge rejected a claim by the U.S. Department of Defense that the Pfizer-BioNTech COVID-19 vaccine being administered under Emergency Use Authorization is interchangeable with Pfizer’s fully licensed Comirnaty vaccine.

ChildrensHealthDefense.org

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A federal district court judge has rejected a claim by the U.S. Department of Defense (DOD) that the Pfizer-BioNTech COVID-19 vaccine being administered under Emergency Use Authorization is interchangeable with Pfizer’s Comirnaty vaccine, which in August was fully licensed by the U.S. Food and Drug Administration (FDA).

In an order issued Nov. 12 in Doe et al. v. Austin, U.S. Federal District Judge Allen Winsor of the U.S. District Court for the Northern District of Florida denied a preliminary injunction requested by 16 service members against the U.S. Military’s COVID vaccine mandate. A hearing is scheduled for Sept. 14, 2022.

However, the judge’s acknowledgment that “the DOD cannot mandate vaccines that only have an EUA” is significant for two reasons.

One reason pertains to the difference in ingredients and manufacturing process between Pfizer’s EUA vaccine and the approved Comirnaty vaccine, and the other pertains to the legal difference between a fully licensed vaccine and an EUA vaccine.

The latter reason would apply not just to the Pfizer-BioNTech vaccine, but also to the vaccines produced by Moderna and Johnson & Johnson (Janssen), both of which are authorized only as EUA products.

TheLibertyDaily.com

It no longer amazes most cognizant Americans to hear that Big Pharma and our own government conspired to promote dangerous “vaccines” to the people. They had their own agendas and saving lives wasn’t among them.

The final batch of Pfizer documents pertaining to Americans 16 and older have been released and they’re as damning as many of us expected. Here’s a breakdown by Twitter user Chief Nerd:

NEW — @ICANdecide Has Received the Final Batch of Pfizer Documents for Ages 16+ and Made Them Available to the Public

See the 🧵 below for observations of particular interest from the 51,893 pages. pic.twitter.com/KyEf7LBKvy

— Chief Nerd (@TheChiefNerd) December 4, 2023

Big Pharma developing a more potent form of experimental gene therapy technology
that will be sold to the public as life-saving 'vaccines.'

TheEpochTimes.com

Infowars.com

When I was looking at the data, which is part of my job, I noticed some discrepancies with the dates of death, people getting people dying within a week of being vaccinated,' says whistleblower.

A database administrator who helped the New Zealand government catalog vaccine recipients has come forward revealing the spike in deaths associated with the Covid-19 jab campaign, which resulted in hundreds dead.

According to the statistician whistleblower, who called himself “Winston Smith,” he worked on a program logging vaccine compensation for providers and was able to pinpoint how deaths began occurring shortly after the vaccine rollout.

TheGatewayPundit.com

Texas Attorney General Ken Paxton has initiated legal action against pharmaceutical giant Pfizer, Inc., citing allegations of deceptive practices related to the company’s COVID-19 vaccine.

The lawsuit asserts that Pfizer engaged in misrepresenting the vaccine’s efficacy, particularly challenging the claim of 95% effectiveness, and accuses the company of trying to stifle public debate on the matter.

Attorney General Paxton accuses Pfizer of violating the Texas Deceptive Trade Practices Act through “false, deceptive, and misleading acts and practices.”

The lawsuit highlights the company’s claims that the vaccine has a 95% efficacy rate against COVID-19 infection, stating that this was based on “relative risk reduction” in Pfizer’s initial short-term clinical trial results

RairFoundation.com

By Maryanne Demasi, PhD
blog.maryannedemasi.com

The recent findings of DNA fragments in the Pfizer and Moderna Covid-19 vaccines has led many to question why the FDA, which is responsible for monitoring the quality and safety of the vaccines, has failed to sound the alarm.

For years, the FDA has known about the risk posed by residual DNA in vaccines. Its own guidance to industry states:

“Residual DNA might be a risk to your final product because of oncogenic and/or infectivity potential. There are several potential mechanisms by which residual DNA could be oncogenic, including the integration and expression of encoded oncogenes or insertional mutagenesis following DNA integration.”

Put simply, the FDA acknowledges the possibility that fragments of DNA left over by the manufacturing process can be incorporated into a patient’s own DNA, to potentially cause cancer.