Quote:He said supply chains would soon be interrupted and urged Aussies to stock up on groceries to get them through the next couple of weeks.

A GoFundMe page has since been launched to support the truckies financially as they prepare to strike from 9am on Tuesday August 31, which will involve 'blocking every highway entering into every state at the same time'. -Daily Mail

For your consideration. Taken from here. Published June 8, 2021



Dear America,

This is the story of possibly the greatest corruption scandal in our country’s history.

This is the story of how petty bureaucrats and drug companies unjustly discredited an inexpensive FDA-approved drug that would have prevented COVID-19 hospitalizations and deaths for political spite and financial gain. These perpetrators, who now hold more significant positions in government, need to be held accountable for over 500,000 American deaths and the disruption of our economy.

This is the story of how a few key government officials failed to implement our well-formulated National Pandemic Plan and their weaponization of a dangerously complicit mainstream media.

I tell this story because we, the People, deserve answers – those responsible need to be held accountable for their actions. The COVID-19 pandemic was a proverbial “warning shot across our bow.” Thus, we must forever prioritize pandemic preparedness as critical to our national security.

We deserve better. We deserve the truth. We deserve answers. We deserve JUSTICE.

I hope my words and timeline will help clarify what has happened, who is involved, and what action must be taken to protect our health and freedom.

My name is Dr. Steven Hatfill. I am a specialist physician, recognized Virologist and Bioweapons expert and I worked as an outside advisor to the Executive Office of the President of the United States from February 2020 through the inaugural transition period of 2021. My statements are not speculation because I had a front-row seat from the very beginning of the pandemic. My subsequent published papers and articles have been painstakingly referenced and fact-checked.

Some will tell you this is just another conspiracy theory, so I ask you to read on and judge for yourselves.

FACTUAL EVENTS

2005 – the United States creates its first-ever National Pandemic Plan, outlining the actions to combat a serious respiratory viral disease pandemic. This is based on the previous Biological Weapons Improved Response Plan.

2008 – President Obama closes the White House Global Health Security Office.

2013 – after the SARS and MERS outbreaks, Chinese virologists collect hundreds of samples from bats for study at the Wuhan Institute of Virology (WIV). Collaborative research begins on the Coronaviruses, including Gain Of Function (GOF) experiments (research which involves increasing the capacity of a pathogen to cause illness) in China and the University of North Carolina at Chapel Hill.

2014 – The West Africa Ebola virus outbreak occurs. Dr. Anthony Fauci MD promotes a single layer of gloves for nursing Ebola patients and other inadequate protective measures. His instructions endanger the lives of health care workers, and national guidelines for protection must be urgently updated.

2014 – United States’ Centers for Disease Control and Prevention (CDC) and the World Health Organization (WHO) ban GOF research. The ban was implemented for 2014-2017.

2015 – Chinese virologists and the University of North Carolina at Chapel Hill conduct unauthorized GOF experiments on coronaviruses.

2017 – The 2005 Health and Human Services’ (HHS) National Pandemic Plan is updated. The specific responsibilities of local authorities, states, and the federal government have been clearly stated. The national plan is to use early, outpatient antiviral drug treatment, home quarantine, and case contact tracing to cover the “vaccine gap” (the time needed to develop a vaccine to combat any pathogen).

December 2019 – Chinese authorities report the first outbreak of COVID-19 in Wuhan. On January 21, the first recognized case of COVID-19 occurs in the United States.

February 2020 – Dr. Steven Hatfill MD, a specialist physician and recognized Virologist, is brought into the White House as an outside medical advisor. Some members of the COVID-19 Task Force are considering the use of Hydroxychloroquine (HCQ), a safe and effective FDA-approved drug, to control the rapidly spreading pandemic. The drug proves to prevent hospitalization if taken when early symptoms of COVID-19 arise. The drug is cost-effective at 60 cents per tablet with COVID-19 treatment consisting of 11 tablets taken over five days. The FDA considers HCQ to be a safer drug than Tylenol.

March 23, 2020 – The Director of BARDA, (Biological Advanced Research Development Authority) Rick Bright Ph.D., is instructed by his superiors to work with the FDA to establish an Investigational New Drug (IND) authorization for HCQ. The next day, the Director of Drug Evaluation and Research at the Food and Drug Administration (FDA), Dr. Janet Woodcock MD, contacts Rick Bright at BARDA.

March 24, 2020 – Dr. Woodcock wrongly advises Bright that HCQ is a dangerous drug requiring a EUA (Emergency Use Authorization). Its use should be limited to hospitalized patients. Bright and Dr. Woodcock promote this course of action, despite the early clinical data showing HCQ was the most effective in outpatients if given early during the initial infection, effectively eliminating hospitalization.

The FDA issues a EUA for HCQ – for hospital use only.

• In a legal document, Rick Bright makes a blatant admission of insubordination to multiple layers of leadership, including the White House, HHS Secretary Azar, and Dr. Robert Kadlec, MD, the Assistant HHS Secretary for Preparedness and Readiness.
  
• Bright states the following in his Whistleblower Complaint: “…instead of a Nationwide Expanded Access IND protocol. Implementing the EUA was a compromise position, to rein in HHS leadership’s initial campaign to make the drugs available to the public outside of a hospital setting“.
  
• Question: When is it EVER acceptable to “compromise” public health during a rampaging pandemic?
  

• All conflicts of interest and the interactions between government officials and pharmaceutical companies, including the publication of faulty research papers in respected medical journals, must be investigated, and they must be held accountable.
  
• Immediately reinstate HCQ as an FDA-approved drug for COVID-19.
  
• The U.S. Pandemic Plan must be immediately reinstated as initially crafted.
  
• Establish an outside independent United States Pandemic Response Department, with board powers including oversight.
  

• Book The Dictator Pope exposes the true Jorge Bergoglio
  
• Omar Bello: Francis Plays Both Sides
  
• Novus Ordo Cardinals slam Francis as “Cold-Blooded, Cunning Machiavellian [who] Lies”, Heretic
  

Quote:Pope Francis could soon promulgate a new law (in the form of an Apostolic Constitution) to regulate the resignation of the Pope, and especially the status following the resignation of a Pontiff.

This is also to avoid a whole series of misleading interpretations on the existence of two Popes, on their cohabitation, on the thesis of “an enlarged papacy” and on other issues which, although not having touched the vast majority of the faithful, have fed the underground poisons of the so-called “Pope-vacantists,” [=“Resignationists”] who have come to hypothesize that the only true Pope is Ratzinger.

In short, it is not even excluded, although it would be sensational, that for the new law there has been no Pope Emeritus at all.

(Maria Antonietta Calabrò, “Francesco potrebbe promulgare una norma sullo status di ‘Papa emerito'”, Huffington Post, Aug. 23, 2021; translation by Robert Moynihan.)

Quote:"We have every expectation that once the vaccines are made mandatory the troops are going to do the right thing," Kirby told reporters at a Pentagon news conference a few weeks ago. "But, without speaking to the future, it’s treated, certainly, like any lawful order, and there could be administrative and disciplinary repercussions for failing to obey that order."

Quote:"Commanders have a range of tools, short of using the UCMJ [Uniform Code of Military Justice] available to them to try to help individuals make the right decisions," Kirby added.

Quote:Today, the U.S. Food and Drug Administration approved the first COVID-19 vaccine. The vaccine has been known as the Pfizer-BioNTech COVID-19 Vaccine, and will now be marketed as Comirnaty (koe-mir’-na-tee), for the prevention of COVID-19 disease in individuals 16 years of age and older. The vaccine also continues to be available under emergency use authorization (EUA), including for individuals 12 through 15 years of age and for the administration of a third dose in certain immunocompromised individuals.

"The FDA’s approval of this vaccine is a milestone as we continue to battle the COVID-19 pandemic. While this and other vaccines have met the FDA’s rigorous, scientific standards for emergency use authorization, as the first FDA-approved COVID-19 vaccine, the public can be very confident that this vaccine meets the high standards for safety, effectiveness, and manufacturing quality the FDA requires of an approved product,” said Acting FDA Commissioner Janet Woodcock, M.D. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated. Today’s milestone puts us one step closer to altering the course of this pandemic in the U.S."

Since Dec. 11, 2020, the Pfizer-BioNTech COVID-19 Vaccine has been available under EUA in individuals 16 years of age and older, and the authorization was expanded to include those 12 through 15 years of age on May 10, 2021. EUAs can be used by the FDA during public health emergencies to provide access to medical products that may be effective in preventing, diagnosing, or treating a disease, provided that the FDA determines that the known and potential benefits of a product, when used to prevent, diagnose, or treat the disease, outweigh the known and potential risks of the product.

FDA-approved vaccines undergo the agency’s standard process for reviewing the quality, safety and effectiveness of medical products. For all vaccines, the FDA evaluates data and information included in the manufacturer’s submission of a biologics license application (BLA). A BLA is a comprehensive document that is submitted to the agency providing very specific requirements. For Comirnaty, the BLA builds on the extensive data and information previously submitted that supported the EUA, such as preclinical and clinical data and information, as well as details of the manufacturing process, vaccine testing results to ensure vaccine quality, and inspections of the sites where the vaccine is made. The agency conducts its own analyses of the information in the BLA to make sure the vaccine is safe and effective and meets the FDA’s standards for approval.

Comirnaty contains messenger RNA (mRNA), a kind of genetic material. The mRNA is used by the body to make a mimic of one of the proteins in the virus that causes COVID-19. The result of a person receiving this vaccine is that their immune system will ultimately react defensively to the virus that causes COVID-19. The mRNA in Comirnaty is only present in the body for a short time and is not incorporated into - nor does it alter - an individual’s genetic material. Comirnaty has the same formulation as the EUA vaccine and is administered as a series of two doses, three weeks apart.

"Our scientific and medical experts conducted an incredibly thorough and thoughtful evaluation of this vaccine. We evaluated scientific data and information included in hundreds of thousands of pages, conducted our own analyses of Comirnaty’s safety and effectiveness, and performed a detailed assessment of the manufacturing processes, including inspections of the manufacturing facilities,” said Peter Marks, M.D., Ph.D., director of FDA’s Center for Biologics Evaluation and Research. "We have not lost sight that the COVID-19 public health crisis continues in the U.S. and that the public is counting on safe and effective vaccines. The public and medical community can be confident that although we approved this vaccine expeditiously, it was fully in keeping with our existing high standards for vaccines in the U.S."

Taken from The Liturgical Year by Dom Prosper Guéranger  (1841-1875)

Quote:Philip was born at Florence of the noble family of the Benizi, and from his very cradle gave signs of his future sanctity. When he was scarcely five months old he received the power of speech by a miracle, and exhorted his mother to bestow an alms on the Servants of the Mother of God. As a youth, he pursued his studies at Paris, where he was remarkable for his ardent piety, and enkindled in many hearts a longing for our heavenly fatherland. After his return home he had a wonderful vision in which he was called by the Blessed Virgin to join the newly-founded Order of the Servites. He therefore retired into a cave on Mount Senario, and there led an austere and penitential life, sweetened by meditation on the sufferings of our Lord. Afterwards he travelled over nearly all Europe and great part of Asia, preaching the Gospel and instituting everywhere the Sodality of the Seven Dolors of the Mother of God, while he propagated his Order by the wonderful example of his virtues.

He was consumed with love of God and zeal for the propagation of the Catholic faith. In spite of his refusals and resistance he was chosen General of his Order. He sent some of his brethren to preach the Gospel in Scythia, while he himself journeyed from city to city of Italy repressing civil dissensions, and recalling many to the obedience of the Roman Pontiff. His unremitting zeal for the salvation of souls won the most abandoned sinners from the depths of vice to a life of penance and to the true love of Jesus Christ. He was very much given to prayer and was often seen rapt in ecstasy. He loved and honored holy virginity, and preserved it unspotted to the end of his life by means of the greatest voluntary austerities.

He was remarkable for his love and pity for the poor. On one occasion when a poor leper begged an alms of him, at Camegliano, a village near Sienna, he gave him his own garment, which the beggar had no sooner put on than his leprosy was cleansed. The fame of this miracle having spread far and wide, some of the Cardinals who were assembled at Viterbo for the election of a successor to Clement IV, then lately dead, thought of choosing Philip as they were aware of his heavenly prudence. On learning this, the man of God, fearing lest he should be forced to take upon himself the pastoral office, hid himself at Montamiata until after the election of Pope Gregory X. By his prayers he obtained for the baths of that place, which still bears his name, the virtue of healing the sick. At length, in the year 1285, he died a most holy death at Todi, while in the act of kissing the image of his crucified Lord, which he used to call his book. The blind and lame were healed at his tomb, and the dead were brought back to life. His name having become illustrious by these and many other miracles, Pope Clement X enrolled him among the Saints.

Begins approx. 3:50 minute mark

Quote:A few major news outlets covered its release by briefly reiterating the study’s summary: that masking then-unvaccinated teachers and improving ventilation with more fresh air were associated with a lower incidence of the virus in schools. Those are common-sense measures, and the fact that they seem to work is reassuring but not surprising. Other findings of equal importance in the study, however, were absent from the summary and not widely reported. These findings cast doubt on the impact of many of the most common mitigation measures in American schools. Distancing, hybrid models, classroom barriers, HEPA filters, and, most notably, requiring student masking were each found to not have a statistically significant benefit. In other words, these measures could not be said to be effective. -NYMag