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The more information that comes out, the more governments are willing to cover up
vaccine data despite a constantly growing public outcry demanding answers.
Josh Sigurdson reports on recent news exposing the FDA as the Food & Drug Administration has been given allowance by US District Judge Reggie Walton to essentially hide vaccine data from the public due to “extraordinary circumstances.”
They knew the shots were killing people from the start and gave orders to conceal deaths.
Del recently visited the laboratory of Pathologist, Dr. Ryan Cole, to get a first-hand look under microscopes to find out what is true, and what is not, about Covid-19 vaccines, along with unusual samples from postmortem vaccinated patients. Then, Del tests his own blood on each one of the Covid Vaccines.
Public willingness to get injected with who-knows-what from vaccine needles is waning. Thus, scientists are now developing needleless vaccines that they claim can be delivered to a person’s body through ultrasound.
At the recent Acoustics 2023 event in Sydney, scientists unveiled the concept along with a press release from the Acoustical Society of America (ASA), which co-hosted the event along with the Australian Acoustical Society.
With funding from the Bill & Melinda Gates Foundation, the Coalition for Epidemic Preparedness Innovations is investing $1.2 million in a startup to create under-the-tongue vaccine wafers that can be stored at any temperature. Critics question the reliability of the technology and the safety of the mRNA platform.
The Coalition for Epidemic Preparedness Innovations (CEPI) is partnering with Jurata Thin Film Inc. to develop a wafer-like mRNA film that can be stored at room temperature and taken under the tongue for needle-free vaccine delivery.
The partnership will begin with a $1.2 million investment to help Jurata develop its proprietary vaccine platform, which the company says stabilizes mRNA-containing lipid nanoparticle vaccine technologies in a thin film.
Jurata claims the film is designed to be “thermostable,” produced and stored at room temperature and remain stable for three years, eliminating the need for energy-intensive cold storage required by current mRNA vaccines.
A study shows that Pfizer vaccines were significantly more likely to produce proteins that some experts believe may increase cancer and autoimmune risk.
There may be around a 1 in 10 chance that Pfizer mRNA COVID-19 vaccines will not generate spike proteins but something else, a new Cambridge study finds, raising concerns about autoimmune response among experts.
The study authors found that 8 percent of the time, Pfizer mRNA COVID-19 vaccines are mistranslated, leading to the formation of unintended proteins.
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.
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.
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
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:
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.
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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.
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