How Fauci Predicted a Worldwide ‘Surprise’
On Tuesday afternoon, November 9, 2021, The New York Times ran an article titled “Moderna and U.S. at Odds over Vaccine Patent Rights.” Reporters Stolberg and Robbins unravel the dispute and the four-year history behind it – which is interesting considering the vaccine in question was for SARS-COV-2, the virus which emerged in late 2019, not 2017.
The fight is about who gets the credit for inventing the primary component of the vaccine, placing long term distribution of this medical product and billions of dollars at stake. It turns out vaccines are big business – especially when they are mandated for every man, woman, and child on the planet.
Big money looms for both manufacturers and the United States Government when producing products exempt from liability. Vaccines were deemed unavoidably unsafe by the United States Congress in 1986 and affirmed unavoidably unsafe by the United States Supreme Court in 2011.
Products which are unavoidably unsafe are technically defined as products that are incapable of being made safe for their intended use. The United States Centers for Disease Control disagrees with the United States Congress and SCOTUS and state that vaccines, especially coronavirus vaccines, are safe and effective. Dr. Anthony Fauci claims they are safe and effective as well.
This NYT article helps explain what the vaccines are ultimately effective at doing.
The four-year collaboration was between Moderna, and 3 scientists associated with the National Institutes of Health (NIH) employed by the Vaccine Research Center (VRC) housed within the National Institute of Allergy & Infections Disease (NIAID) under the leadership of Dr. Fauci. The VRC was established by Bill Clinton and named after Dale and Betty Bumpers of Arkansas.
Betty Bumpers worked hand in hand with Roslyn Carter to establish the nonprofit organization Every Child by Two (ECBT) in 1991 to promote full coverage vaccination of toddlers within the first two years of life. The organization proudly rebranded to Vaccinate Your Family in 2018.
By 1993, Mrs. Bumpers and Mrs. Carter had traveled to all 50 states to help establish immunization coalitions of policymakers, organizations, and concerned citizens. ECBT boasted in 1998 on their website that “These two women have been credited with the passage of laws mandating vaccination at school entry, which now exist in every state. As a result of these laws, the United States has a 95% plus immunization rate for school enterers.”
The Dale & Betty Bumpers VRC explains their mission in their agency brochure. The VRC is highly focused on the development of gene-based vaccine technology platforms.
In addition, the brochure clarifies the VRC “develops new vaccine platforms, such as genetic vaccination and nanoparticle display. Design and engineering are product driven and consist of (1) process development, which is an overarching term referring to processing methods (e.g., designing appropriate cell culture media), analytical tools (e.g., measuring product yields and purity), and formulation methods (e.g., ensuring stability in the vial for clinical products); and (2) the manufacture of pilot lot clinical materials.”
Developing this platform makes it easier to grow the vaccine manufacturing market to address as many viruses as the government deems a threat to the public to ensure our peace and safety. The government agencies define the word “threat.”
More vaccines in the future using this rapid platform deployed during the public/private partnership of Operation Warp Speed can bring new vaccines to market within a desired goal of 230 days rather than decades of development as outlined in President Biden’s American Pandemic Preparedness plan.
Moderna filed several patents for this technology well before the Covid-19 pandemic appeared: January 6, 2018, September 4, 2018, April 23, 2019, and October 15, 2019. Their platform was ready as soon as they received the genetic sequence code for the SARS COV-2 virus which was supplied by China on January 11, 2020. Only 41 people in the world had contracted coronavirus by January 11th and although they had never brought a vaccine to market before, Moderna knew this was the big one they had been waiting for. They got right to work developing a vaccine.
It was well known, according to the NYT article, that the NIH and Moderna had been in collaboration for four or five years on developing mRNA vaccines. In addition to the Coronavirus vaccine, Moderna has vaccines lined up for patents for cytomegalovirus, respiratory syncytial virus, flu, Zika, HIV, propionic acidemia and methylmalonic acidemia – which are inborn errors of metabolism, personalized cancer vaccines, myocardial ischemia, Ebola and Nipah viruses.
What does this mean?
This means Moderna and the NIH developed a platform that can be quickly used to develop genetic vaccines to address viruses, as well as conduct gene therapy on the DNA you, or your children, possessed when born. They are fighting about who gets to control and profit from that platform.
Basically, Moderna and NIH developed this cookie recipe together, but Moderna developed the technology to cut the cookies into certain shapes and decorate them. Now the NIH wants profits off of both the cookie recipe and the final baked cookie product as well.
Sales of the Moderna vaccine in 2021 and 2022 are anticipated to rank among the highest sales in a single year for any medical product in all of history. Makes you wonder what kind of money unavoidably unsafe products made from all the viruses and genetic defects science can possibly identify will generate – especially since they aren’t liable for any damages.
You may recall that Dr. Anthony Fauci prophetically predicted nearly 5 years ago that something was coming during the Trump administration that would really be a challenge back on January 11, 2017. He stated, “A surprise is coming.”
And he added, “There is no question there will be a challenge in the coming administration in the arena of infectious diseases, both chronic infectious diseases in the sense of already ongoing disease. And we have certainly a large burden of that. But also, there will be a surprise outbreak. And I hope that the end of my relatively short presentation will (help you) understand why the history of the last 32 years that I have been the director of NIAID will tell the next Administration (Trump) that there is no doubt in anyone’s mind that they will be faced with the challenges that their predecessors were faced with.”
He was correct, but maybe now we know why.
They’ve been laying the groundwork for decades.
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Author Shelley McLaughlin is a passionate IFA intercessor who loves meditating on His Word. Picture Credit: Getty Images.
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