There is no longer science-based medicine in the United States.

Medicines are primarily produced and promoted by a public-private partnership between federal bureaucrats and Big Pharma to enhance government power and amass personal profit.

Curing disease is a secondary consideration. In fact, prolonging disease is more profitable.

The Daily Clout has published 55,000 Pfizer documents, which the U.S. Food and Drug Administration (FDA) had asked the court to keep secret for 75 years.

Thousands of doctors, nurses, biostatisticians, medical fraud investigators, laboratory clinicians and research scientists are now analyzing and posting what those previously secret documents reveal – a massive number of shocking lies the world has been told about the COVID-19 vaccines.

A summary of those findings has been published by Dr. Naomi Wolf.

First and foremost amongst them is the fact that Pfizer and the FDA knew by December 2020 that the mRNA vaccines did not work — that they “waned in efficacy” and presented “vaccine failure.”

Pfizer knew in May of 2021 that 35 minors’ hearts had been damaged a week after mRNA injection.

According to Wolf’s summary, while pregnant women were excluded from the internal studies, and thus from the Emergency Use Authorization on which basis all pregnant women were assured the vaccine was “safe and effective”, nonetheless about 270 women got pregnant during the study. The records of more than 230 of them were somehow “lost.” But of the 36 pregnant women whose outcomes were followed – 28 lost their babies.

Many babies nursing from vaccinated mothers showed agitation, gastrointestinal distress, and failure to thrive (to grow), and were inconsolable.

et, the FDA is now moving to approve COVID-19 mRNA vaccines for children 6 months through 5 years of age.

All of this vaccine insanity could have been avoided simply by transparency and “following the science.”

The Pfizer and Moderna COVID-19 vaccines were designed to produce immunity by injecting genetic material (mRNA) into muscle cells, which would use the cells’ own mechanisms to synthesize spike proteins that would then generate antibodies circulating inside our bodies to bind to and block the ability of COVID-19 spike proteins to initiate the infection process.

Unfortunately, it was later learned, long after the global human experimentation began, that the vaccine, a lipid nanoparticle containing the spike protein mRNA, can spread beyond the local injection site entering other organs, like the heart.

The spike proteins themselves, which are produced by the mRNA, can also circulate throughout the body, having potential cascading damaging effects.

The potential for coronavirus spike protein-induced disease was already known in a 2005 experiment done with SARS-CoV-1, the coronavirus that caused the first SARS pandemic from 2002 to 2004.

That 2005 study found that the 2002-2004 SARS-CoV-1 virus entered human cells by binding to the angiotensin converting enzyme type-2 (ACE2) receptor and both SARS-CoV-1 infection and the spike protein alone reduced ACE2 expression, thus dysregulating the renin-angiotensin-aldosterone system (RAAS) responsible for a variety of critical bodily functions.

More ominously, however, the 2005 scientific publication reported that treatment of the laboratory animals with just the small ACE2 binding component of the spike protein made subsequent SARS-CoV-1 lung infections worse.

The spike protein of the COVID-19 virus can similarly interact with RAAS leading to reduced cardioprotection, increased lung injury, contributing to atherosclerosis, hypertension, heart failure, and chronic kidney disease, as well as creating the conditions for the formation of blood clots.

The point being is that, because of scientific censorship, “we don’t know what we don’t know,” and American citizens have been denied informed consent, while being subjected to forced vaccination with an experimental and potentially highly dangerous vaccine.

The preponderance of evidence now shows that COVID-19 mRNA vaccines do not prevent infection or transmission, are only short-acting if at all, do not significantly affect viral load of infected individuals and may enhance the transmission of viral variants.

In contrast to any beneficial effect, COVID-19 mRNA vaccines may exacerbate pre-existing conditions or cause acute or chronic pathogenic effects, both in the presence and absence of COVID-19 infection, by dysregulating delicately-balanced bodily functions or initiating damaging immune, inflammatory or blood-clotting processes.

Taking COVID-19 mRNA vaccines may be a bit like leaning into a punch.

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Lawrence Sellin, Ph.D. is retired U.S. Army Reserve colonel and a veteran of Afghanistan and Iraq. He had a civilian career in international business and medical research. Dr. Sellin is the author of Restoring the Republic: Arguments for a Second American Revolution. His email address is [email protected].

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