WHAT WENT WRONG IN THE GOVERNMENT'S RESPONSE TO THE PANDEMIC AND HOW DO WE STOP IT FROM HAPPENING AGAIN?
Stay tuned for June 27, 2022, Senate Health and Human Resources Committee Hearing on the Pandemic Response.
07/23/21 Despite the failure of the PCR test and contrary to reports from various countries showing that the Delta variant is predominately infecting vaccinated people, US media outlets are falsely accusing the unvaccinated of rising COVID-19 cases.
07/23/21 The FDA announced today that the CDC PCR test for COVID-19 has failed its full review. After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only.
07/23/21 Boston Globe In Singapore, 75 percent of COVID infections are among vaccinated and partially vaccinated people,
07/25/21 New South Wales, Australia report 141 new cases, all fully vaccinated but one only had one shot.
On July 19th, America's Frontline Doctors filed suit against
US Health and Human Services for underreporting of vaccine injury via the Vaccine Adverse Events Reporting System (VAERS)
Sworn affidavit, of a whistleblower who has access to the Centers for Medicare and Medicaid Services (CMS) system analyses data from
VAERS compared to CMS and states,
"On July 9, 2021, there were 9,048 deaths reported to VAERS. ... In tandem, I queried data from the CMS claims with regard to vaccines and patient deaths, and have assessed that the deaths occurring within 3 days of vaccination are higher than those reported in VAERS by a factor of at least 5. This would be indicated that the true number of vaccine-related deaths was at least 45,000."
On July 9, 2021, VAERS reported 9 short of 11,000 deaths. If the 5x factor is true, this represents 55,000 deaths from COVID-19 gene-modifying technology referred to as vaccines.
What did they know and when did they know it?
See the "anticipated side effects from COVID-19 vaccines" on
slide 16 of the CBER Plans for Monitoring COVID-19 Vaccine Safety and Effectiveness meeting presentation from the
October 22, 2020 Vaccines and Related Biological Products Advisory Committee.
Must see July 12, 2021 deposition style interview of
Dr. David Martin with Reiner Fuellmich.
On July 12, 2021, Dr. David Martin, founder of MCAM CNBC IQ100 index, was interviewed by Reiner Fuellmich in this 1:22:47 minute video.
Sheila Hemphill's brief message from Dr. Martin
“The Pandemic is a racketeering, criminal conspiracy managed by Anthony Fauci, Peter Daszak, and Ralph Baric outlined in the attached Fauci Dossier document. It is essential for the State Texas Attorney General to file racketeering charges against these individuals, for “Terror to coerce a population” in violation of Section 802 of the USA Patriot Act.”
- The Fauci Dossier - Must see a timeline of patents awarded, pg 20
SARS CoV Patent Corpus summary of patents pertaining to SARS CoV.
A rough transcription of the video with minute markers.
Who is Dr. David Martin?
Minute Marker 00:18:00
“From a corporate standpoint, we have, since 1998, been the world's largest underwriter of intangible assets used in finance in 168 countries. So in the majority of the countries around the world, our underwriting systems include the entire corpus of all patents, patent applications, federal grants procurement records, e-government records, etc. We have the ability to not only track what is happening and who is involved in what's happening, but we monitor a series of thematic interests for a variety of organizations and individuals, as well as, for our own commercial use because as you probably know we maintain three global equity in the indices which are the top-performing large-cap and mid-cap equity indexes worldwide. So our business is to monitor the innovation that's happening around the world and specifically to monitor the economics of that innovation to the degree to which you know financial interests are being served, you know corporate interests are being dislocated, etc. So our business is the business of innovation and its foreign finance industry of social innovation."
Minute marker 00:09:25
On April 19, 2002 – the Spring before the first SARS outbreak in Asia – Christopher M. Curtis, Boyd Yount, and Ralph Baric filed an application for U.S. Patent 7,279,372 for a method of producing recombinant coronavirus. In the first public record of the claims, they sought to patent a means of producing, “an infectious, replication-defective, coronavirus.” This work was supported by the NIH grant referenced above and GM63228. In short, the U.S. Department of Health and Human Services was involved in the funding of amplifying the infectious nature of coronavirus between 1999 and 2002 before SARS was ever detected in humans. (Fauci Dossier pg 3)
What is the end-game of the pandemic?
From David Martin regarding Peter Daszak, EcoHealth, recipient of NIH, NIAID, etc. funding.
Minute marker 00:29:26
“The statement that was made by Peter Daszak in 2015 was reported in the National Academies of press publication February 12, 2016. I'm quoting,
“We need to increase public understanding of the need for medical measures such as a pan coronavirus vaccine. A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues, investors will respond if they see profit at the end of the process.”
Minute marker 00:31:37
“The person who was independently corroborating the Chinese non-lab leaked, non-theory because there wasn't a lab leak this was an intentional bio weaponization of spike proteins to inject into people to get them addicted to a pan coronavirus vaccine. This has nothing to do with a pathogen that was released and every study that's ever been launched. To try to verify a lab leak is a red herring and there's really nothing that is new in this nothing.”
Minute marker 00:34:57
“The script for this was written first January 6, 2004, who wrote the script before a conference called SARS and Bioterrorism Emerging Infectious Diseases, Antimicrobials Therapeutics, and Immune Modulators. Merck introduced the notion of what they, called, “The New Normal” proper noun. The New Normal, which is the language that became the branded campaign that was adopted by the world health organization global preparedness monitoring board, which was the board upon which the Chinese director of Center for Disease Control, Bill Gates's, Dr. Elias of the Gates Foundation, and Anthony Fauci sat together on that board of directors but the first introduction of the new normal campaign which was about getting people to accept universal pan influenza, pan coronavirus vaccine.”
Minute marker 00:39:00
“What makes that story most problematic beyond the self-evident nature of it, is that we know that from 2016 until 2019, at every one of the National Institute of Allergy and Infectious Disease (NIAID) advisory council board meetings, Anthony Fauci lamented the fact that he could not find a way to get people to accept the universal influenza vaccine.”
AND MUCH, MUCH MORE!
The corrupt actions of Anthony Fauci, Peter Daszak, and Ralph Baric represent the most aggressive crimes against humanity imaginable.
Attempts to communicate to laypeople, legislators, and law enforcement about the corruption of Anthony Fauci, NIH, Peter Daszak, Ecohealth, and Ralph Baric, University of South Carolina, through scientific and medical studies are very difficult. The subject is highly complex, the terms are unfamiliar
Dr. David Martin's Fauci Dossier contains irrefutable evidence that documents the corruption and strong delusion of this Pandemic through the tracking of patents awarded to CDC, NIH, NIAID, and various pharmaceutical complies like Pfizer, Moderna, and many others.
Why is the CDC and COVID-19 vaccine manufacturers pushing so hard to get 12-17-year-olds in vaccine trials when this age group's chance of dying from COVID-19 is less than 1%?
Vaccines manufacturers and health care providers and private businesses, aka "covered persons", are not liable for any vaccine injury under the Public Readiness and Emergency Preparedness Act for vaccines licensed under Emergency Use Authorization (EUA) for Vaccines to Prevent COVID-19. In the event that the COVID-19 vaccines receive FDA approval, the "covered persons" will be liable unless the COVID-19 vaccine becomes part of the childhood vaccine schedule shielding them from liability with the
National Childhood Vaccine Injury Act of 1986.
The Omega Brief:
Irrefutable patent evidence of premeditated actions seen during the pandemic.
Text "DEFEND" to 855-822-1010 for Action Alerts
From 21 USC 360 bbb-3
Emergency Use Authorization (EUA) Criteria from page 3.
"There is no adequate, approved, and available alternative to the product for diagnosing, preventing, or treating the disease or condition."
Is this EUA criteria along with the CDC Therapeutic Options and NIH COVID-19 Treatment Guidelines the reason they have prevented early treatment so they could get the vaccine roll-out?