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This article was first published by Patrick Wood in Technocracy News and Trends and is reproduced here by his kind permission

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Story at a glance

  • Trump signed Executive Order 13887 well before COVID hit
  • It set the stage for mRNA and DNA injections
  • It turned over design, manufacturing and distribution to the military
  • It set up a huge private-public partnership with Big Pharma
  • It set up a task force co-headed by the Secretary of Defense
  • Operation Warp Speed confirmed the design, manufacturing and distribution by the military

It is inconceivable that this editor missed former President Trump’s Executive Order EO 13887 on September 19, 2019, titled Modernizing Influenza Vaccines in the United States To Promote National Security and Public Health. Since then, it apparently has been swept under the carpet, virtually scrubbed from the Internet. Nevertheless, I found it, and this changes everything about Trump’s role in the biggest health fiasco in our nation’s existence.

Before you all attack dogs launch at me, be aware I voted for Trump. I have previously given him every benefit of the doubt on his role in starting Operation Warp Speed and his role with characters like Anthony Fauci, Deborah Birx, and Francis S. Collins. Certainly, he was just used or perhaps duped, right?

Ah, not so fast. The EO 13887 that Trump signed on Sept. 19, 2019, was just before COVID hit. It was one month BEFORE the now-infamous Event 201 role-playing exercise where the elitist response to COVID was carefully laid out. It was before anyone in the public sphere had even conceived that there was a new “vaccine” technology based on genetic engineering that would soon spring into existence, turning Americans into guinea pigs without so much as an “informed consent” form. Safe and effective, they said. No matter that you would get your shot under an Emergency Use Authorization (EUA), in lieu of any safety trials. Trust us, they said.

Since Trump signed EO 13887, we need to see what it says. 

The setup, Section 1 (a):

Periodically, new influenza A viruses emerge from animals, including birds and pigs, that can spread efficiently and have sustained transmission among humans. This situation is called an influenza pandemic (pandemic). Unlike seasonal influenza, a pandemic has the potential to spread rapidly around the globe, infect higher numbers of people, and cause high rates of illness and death in populations that lack prior immunity. While it is not possible to predict when or how frequently a pandemic may occur, there have been 4 pandemics in the last 100 years. The most devastating pandemic occurred in 1918–1919 and is estimated to have killed more than 50 million people worldwide, including 675,000 Americans.

The complaint, Section 1 (d):

The current domestic enterprise for manufacturing influenza vaccines has critical shortcomings. Most influenza vaccines are made in chicken eggs, using a 70-year-old process that requires months-long production timelines, limiting their utility for pandemic control; rely on a potentially vulnerable supply chain of eggs; require the use of vaccine viruses adapted for growth in eggs, which could introduce mutations of the influenza vaccine virus that may render the final product less effective; and are unsuitable for efficient and scalable continuous manufacturing platforms.

Thus, the traditional method of creating vaccines is declared dangerous (“could introduce mutations”)  and inadequate (“unsuitable for efficient and scalable continuous manufacturing platforms”.)

The Solution Announced, Section 2:

This order directs actions to reduce the United States’ reliance on egg-based influenza vaccine production; to expand domestic capacity of alternative methods that allow more agile and rapid responses to emerging influenza viruses; to advance the development of new, broadly protective vaccine candidates that provide more effective and longer lasting immunities; and to support the promotion of increased influenza vaccine immunization across recommended populations.

Alternative methods? More agile and rapid responses? Longer lasting immunities? Hmm.

The Solution Revealed

The EO excessively (in 4 separate sections) talked about cell-based and recombinant vaccines but who knew what this meant?

Sec. 4 (A) estimate the cost of expanding and diversifying domestic vaccine-manufacturing capacity to use innovative, faster, and more scalable technologies, including cell-based and recombinant vaccine manufacturingthrough cost-sharing agreements with the private sector, which shall include an agreed-upon pricing strategy during a pandemic;

Sec. 4 (G)(iii)(C) further support the conduct, in collaboration with the DOD, BARDA, and CDC, of applied scientific research regarding developing cell lines and expression systems that markedly increase the yield of cell-based and recombinant influenza vaccine manufacturing processes;

Sec. 4 (G)(iv)(A) expand vaccine effectiveness studies to more rapidly evaluate the effectiveness of cell based and recombinant influenza vaccines relative to egg-based vaccines

Sec. 4 (b)(v) investigate, in collaboration with HHS, alternative correlates of immune protection that could facilitate development of next-generation influenza vaccines; (vi) direct the conduct of a study to assess the feasibility of using DOD’s advanced manufacturing facility for manufacturing cell-based or recombinant influenza vaccines during a pandemic;

What is “recombinant” you ask? Cambridge Dictionary defines it as “produced by combining genetic material from different places”. Merriam-Webster tell us that is “relating to or containing genetically engineered DNA” and “produced by genetic engineering”.

EO 13887 did not mention the words mRNA, DNA or genetic engineering. Thus, even if you had read the whole thing, you would not have understood what it was a talking about. Now that you know what “recombinant” is, you know it was all about SYNTHETIC mRNA and DNA!!

Enter the Public-Private Partnership

The above Sec. 4 (A) states specifies how the government will participate with Big Pharma to provide:  “cell-based and recombinant vaccine manufacturingthrough cost-sharing agreements with the private sector, which shall include an agreed-upon pricing strategy during a pandemic.” 

“Private sector” means Big Pharma, period. Why does Big Pharma need to use taxpayer funds to promote its insane profiteering juggernaut?

Worse, Enter the Department of Defense

The DOD was charged with design of the mRNA/DNA shots? And, to use its own manufacturing facilities to make the shots? Then, under project Warp Speed it was tasked to deliver the shots to every nook and cranny in America? Read it for yourself:

(iv) identify opportunities to use DOD’s vaccine research and development enterprise, in collaboration with HHS, to include both early discovery and design of influenza vaccines as well as later-stage evaluation of candidate influenza vaccines;

(v) investigate, in collaboration with HHS, alternative correlates of immune protection that could facilitate development of next-generation influenza vaccines; (vi) direct the conduct of a study to assess the feasibility of using DOD’s advanced manufacturing facility for manufacturing cell-based or recombinant influenza vaccines during a pandemic;

Folks, this fully outs the military’s end-to-end role from design, to manufacturing to distribution.

Enter the National Influenza Vaccine Task Force

Notice that the first co-chair of this Task Force is the Secretary of Defense (Mark Esper) who was assisted by the Secretary of Health and Human Services (Alex Azar, the former president of Eli Lilly and Company).

There is hereby established a National Influenza Vaccine Task Force (Task Force). The Task Force shall identify actions to achieve the objectives identified in section 2 of this order and monitor and report on the implementation and results of those actions. The Task Force shall be co-chaired by the Secretary of Defense and the Secretary of Health and Human Services, or their designees.

(b) In addition to the Co-Chairs, the Task Force shall consist of a senior official from the following executive branch departments, agencies, and offices:

(i) the Department of Defense (DOD);

(ii) the Department of Justice;

(iii) the Department of Agriculture;

(iv) the Department of Veterans Affairs (VA);

(v) the Department of Homeland Security;

(vi) the United States Food and Drug Administration;

(vii) the Centers for Disease Control and Prevention;

(viii) the National Institutes of Health (NIH);

(ix) the Centers for Medicare and Medicaid Services (CMS); and

(x) the Biomedical Advanced Research and Development Authority (BARDA).

All of these had a hand in the unfolding of the Great Panic of 2020 and the disastrous and deadly rollout of shots that killed hundreds of thousands of Americans, that destroyed our economy and drove millions into poverty.

Enter “Event 201”

Thirty days later, Event 201 took place on Friday, October 18, 2019, bringing industry leaders to stage a simulation on how COVID and the shots would roll out. It was headed by the director of Center for Health Security, a non-profit organization associated with John Hopkins. Feast your eyes on the “players” who showed up with dollar signs in their eyes:

Latoya Abbott Risk Management/Global Senior Director Occupational Health Services Marriott International
Sofia Borges Senior Vice President UN Foundation
Brad Connett President, U.S. Medical Group Henry Schein, Inc.
Christopher Elias President, Global Development division Bill & Melinda Gates Foundation
Tim Evans Former Senior Director of Health World Bank Group
George Gao Director-General Chinese Center for Disease Control and Prevention (China CDC)
Avril Haines Former Deputy Director Central Intelligence Agency; Former Deputy National Security Advisor
Jane Halton Board member ANZ Bank; Former Secretary of Finance & Former Secretary of Health, Australia
Matthew Harrington Global Chief Operating Officer Edelman
Martin Knuchel Head of Crisis, Emergency and Business Continuity Management Lufthansa Group Airlines
Eduardo Martinez President, The UPS Foundation
Stephen Redd Deputy Director for Public Health Service and Implementation Science US Centers for Disease Control and Prevention
Hasti Taghi Vice President & Executive Advisor NBCUniversal
Adrian Thomas Vice President, Global Public Health, Johnson & Johnson
Lavan Thiru Chief Representative Monetary Authority of Singapore

Enter Operation Warp Speed

The first news story on Operation Warp Speed was April 29, 2020, nine months after EO 13887 was signed.

According to Wikipedia,

Operation Warp Speed (OWS) was a public–private partnership initiated by the United States government to facilitate and accelerate the developmentmanufacturing, and distribution of COVID-19 vaccines, therapeutics, and diagnostics. The first news report of Operation Warp Speed was on April 29, 2020, and the program was officially announced on May 15, 2020.

Just as it was laid out in Executive Order 13887 above. Verbatim. Coincidence? Hardly.

In sum, COVID and the mRNA injections that followed made a mockery of “Make America Great Again.” In fact, it was the ultimate betrayal of the dream and instead turned it into a nightmare. To reiterate, the chain of events kicked off by Trump’s signature destroyed the American economy, killed hundreds of thousands, harmed millions, ripped families apart, and destroyed thousands of churches and businesses along the way.

Do you see Technocrats at work in this? We have been played by these monsters of tyranny. We have been betrayed once again. Unfortunately for him, there are no free passes left for Trump.

Unfortunately for us in 2024, MAGA chants are morphing into a simulacrum, a distant illusion of the promise of a former reality.

Copyright Coherent Publishing, LLC 2016-23

ABOUT THE EDITOR

Patrick Wood
Patrick Wood is a leading and critical expert on Sustainable Development, Green Economy, Agenda 21, 2030 Agenda and historic Technocracy. He is the author of Technocracy Rising: The Trojan Horse of Global Transformation (2015) and co-author of Trilaterals Over Washington, Volumes I and II (1978-1980) with the late Antony C. Sutton.
 
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