On August 23, 2021, the COVID-19 laws of warfare could have changed if evidence had prevailed over blind trust in experts.

On August 23, 2021, the FDA approved PFIZER’s COVID-19 vaccines, COMIRNATY. On August 25, 2021, I appeared on the Stew Peters Show in an interview captioned, “Check Mate. We Win.” Why did I proclaim this victory? Because when the FDA approved PFIZER’s COMIRNATY;

  • PFIZER had to provide a full list and description of the lipid nanoparticle technology that’s in the injections under 21 USC 814.9 within 2 weeks of approval.
  • The FDA had to shift from passive (VAERS) to active (BEST) near-real time surveillance of all US residents aged 16 or older who are in the BEST database and were diagnosed with a symptom, disease, or death after receiving PFIZER’s COVID-19.
    • This data can be released and should be demanded to be released under FOIA.
  • The civil and criminal liability SHIELD for PFIZER was BROKEN, causing the Pharma giant to be in violation of literally hundreds of federal and state laws.

On August 31, 2022, the DOD Defense Logistic Agency, confirmed under a FOIA request, that they began shipping PFIZER’s FDA-approved COMIRNATY to military bases in June of 2022. For over a year, the American people and many legal teams have been misled into believing the FDA never broke PFIZER’s shield.

  • Some still believe the FDA approval didn’t happen, despite the reality that PFIZER’s FDA-approved COMIRNATY has been manufactured and shipped to our military.

Experts, such as Dr. Robert Malone, with highly-impressive credentials in mRNA, vaccinology, and the FDA approval process, stated that the FDA approval was not for a PFIZER COVID-19 vaccine, but for a vaccine made by BioNTech, so ‘it didn’t really happen’. These are false and deceptive statements.

I break down the false claims made by Dr. Malone on August 24, 2021 with documentation and guidance in this SubStack.

Corporate sabotage is very real and prevalent in Big Pharma and Med Device. Typically it is someone who comes from a competitive company, has extremely impressive credentials, and has rightfully earned a position of power and influence. Individuals who commit corporate sabotage can mislead entire corporations because they are well-trusted due to their impressive credentials and ability to network and connect with key individuals and organizations.

If Dr. Malone had been the Executive Vice President of Regulatory/FDA-Approvals at a Big Pharma/Med Device company that received FDA-approval of a medical device, drug, or ‘vaccine’, and then somehow convinced the marketing, sales, executive, regulatory, and even the legal team, that the FDA-approval ‘didn’t really happen,’ and kept the deception going on for over a year, he would have been fired, escorted out by security, and criminally investigated for corporate sabotage.

The false claims made by Dr. Malone caused unnecessary chaos and confusion in our battle to save our country and our children. We must remain united, but we must be united under God and in TRUTH, not under deceptive practices and in blind trust.

I have worked on the commercialization of many FDA-approved pharma products and medical devices. I was the Senior/Executive manager at agencies who finalized the talking points for doctors and messaging for consumers in adherence with FDA compliance guidelines and law. I’ve signed off on packaging and to ‘lift the watermark’ on the final FDA-approved packaging and labeling for purposes of going to mass print production for an FDA-approved product.

On August 25, 2021, I had the documentation and professional expertise to notify the American people of this victory and partner with attorneys to begin a new battle on even ground now that the EUA shield was broken. Somehow, my offers to help win this battle with documents from the FDA, DOD, HHS, and PFIZER fell on deaf ears.

Here are a few examples the opportunities lost and harm done by the mass deception that the FDA-approval of PFIZER’s COVID-19 vaccines, ‘didn’t really happen.’

PFIZER had to provide a full list and description of the lipid nanoparticle gene-editing and neurotechnologies that are in the injections under 21 USC 814.9 within 2 weeks of approval.

  • The mRNA ‘vaccine’ patents state that the lipid nanoparticles have diagnostic applications. A diagnostic is a device and subject to 21 USC 814.9.
  • Under 21 USC 814.9, PFIZER and the FDA/Centers for Device and Radiological Health (CDRH) could have been forced to disclose the Ai nanotechnology in the shots.
  • This would have changed the COVID-19 laws of warfare.
  • An Ai neurotechnology can be used a neuroweapon in warfare or as a medical device in healthcare.
  • Professor James Giordano, DOD IAC, has clearly articulated on the HDAIC website that the use of neuroweapons on the general population may not be illegal if they are used under healthcare and medical experimentation and in partnership with a private sector partners, where due to intellectual property laws, transparency would not be required.

    In legal reality, CBER did not even have the authority to authorize or approve the COVID-19 vaccines because the vaccines contain electronic devices that emit radiation, Qdot. The Center for Devices and Radiological Health (CDRH) would be in receipt of the Qdot PMA and is the responsible division of the FDA for authorization and approval.

  • If this information had not been discredited due false claims about the FDA-approval made by highly-trusted experts such as Dr. Malone, informed consent regarding what is in the vials could have been forced to be known under the laws of warfare our enemies seem to be operating under.

    Thank you for reading The Kingston Report. This post is public so feel free to share it.


The FDA had to shift from passive (VAERS) to active (BEST) surveillance of all US residents aged 16 or older who are in the BEST database and were diagnosed with a symptom, disease, or death after receiving PFIZER’s COVID-19. This data can be released and should be demanded to be released under FOIA.

  • Prior to FDA-approval, the reporting of any side-effect (symptom, disease or death) caused by PFIZER’s COVID-19 injections was passive, consisting mostly of VAERS and PFIZER’s responsibility to notify the FDA if they observed any ‘safety outcomes of interest’.
  • After FDA approval, the side-effect reporting system became active.
  • Active means that the FDA’s CBER/CDRH were obligated to take an active role with near real-time surveillance of side-effects and safety outcomes of interest (disease, disabilities and death) using the BEST and Centers for Medicare and Medicaid electronic healthcare records (EHR) system.
  • BEST provides access to over 300 million patients files…
  • …and billons of healthcare claims.
  • Under FOIA, the American people can demand to know every symptom, disease or death that has been reported by a US resident over the age who has received a PFIZER COVID-19 vaccine, and over the age of 18 who has received a MODERNA COVID-19 vaccine.
  • This data can be demanded using the CPT (Current Procedural Terminology) codes for the FDA-approved COVID-19 ‘vaccine’ age groups for PFIZER and COMIRNATY.
  • By providing the vaccine CPT codes with a list of the ICD-10 (international codes for disease), Americans can obtain nearly EVERY side effect, symptom, disease and death that has been caused by the PFIZER and MODERNA shots within the FDA-approved age groups.
  • A report using ICD-19 codes should be run separate due to the inability or unwillingness of healthcare workers to report vaccine side effects.
  • The BEST system uses IBM Watson, and the data can be exported and downloaded as a .csv file using a Python C++ API fairly quickly.
  • Due to the lack of responsiveness from the FDA/CBER and likely the Centers for Devices and Radiological Health (CDRH), the FOIA requests should go directly to the Chief Technology Officer of Health & Human Services, Karl Matthias.
  • The data regarding the disease, disabilities and death caused by the PFIZER COVID-19 injections for US residents aged 16 and older could have been demanded under FOIA immediately after the August 23, 2021, FDA approval.
  • No action was taken to access these databases because Americans had been deceived into believing the FDA approval ‘didn’t really happen.’

On August 23, 2021, the civil and criminal liability shield for PFIZER was broken, causing the Pharma giant to be in violation of literally hundreds of federal and state laws.

  • The changes in the legal landscape are too vast to enumerate on in a SubStack.I continue to search for colleagues, partners and attorneys who value expertise and knowledge and are invested in winning the war against COVID-19.

On August 23, 2021, the COVID-19 laws of warfare could have changed if evidence had prevailed over blind trust of experts.

We must remain united, but we must be united under God and in TRUTH, not under deceptive practices and in blind trust.

The Kingston Report. TRUTH WINS.

It’s Time we Reunite as Humanity and Take Down COVID-19.

  • STOP all COVID-19 emergency powers and financial funding
  • Ban and recall all COVID-19 products and technologies
  • Take Down 5G

If you would like to support the Take Down of COVID-19, please join miFight.

SOURCE: https://karenkingston.substack.com/p/part-3-dismantling-the-deceptions

A Note From HopeGirl


I believe Karen Kingston was led by God to read through thousands of pages of patents and government documentation, and was shown by the Holy Spirit the most undeniable proof of what has been done to the human race through the COVID-19 vaccines. Her interviews have had many millions of views and many people have come forward saying that it was because of the information Karen Kingston researched that caused them to not get the COVID injections and saved their lives.

Karen was targeted for this work. They tried to poison her on several occasions and we strongly believe that she was targeted by direct energy weapons.  They got to her family and they used typical COINTEL-PRO tactics to try to gaslight her and portray her as “not being well” or “acting crazy” due to malaria drugs. She fled for her life and left her country to go to Mexico and made a video from Mexico pleading for her life and asking that her name be taken off a hit list.   Many people reached out to Karen during this time, including ourselves, Karen did not respond to most people. One can only assume that they got to her. After a couple of weeks she returned to the US and went on two interviews recanting her information. And then she came out on her paid substack formally stating that she has officially decided to resign from doing any additional analysis on mRNA or COVID-19.

In the book of Esther, God commissioned Esther to be the one unique voice to speak out and save his people from perishing. Esther was married to the King and was the one person who could speak to him to stop the planned slaughter of thousands of people. In those times no one could speak to the king without being summoned first and the penalty to do so was death.  I believe Karen is a lot like Esther in this respect. NO ONE was able to put together the information that was in those patents the way Karen did. I’ve spent many hours buried in Karens work and it is obvious to me that she was divinely guided to speak to the world the truth of what was in the shots.

When Esther’s relative Mordecai revealed to her the evil plan to slaughter her people and asked her to speak out to save them, Esther hesitated, fearing for her own life if she spoke out. Mordecai replied to Esther: “Do not imagine that because you are in the king’s palace you alone will escape the fate of all the Jews. For if you remain silent at this time, relief and deliverance for the Jews will arise from another place, but you and your father’s house will perish. And who knows if perhaps you have come to the kingdom for such a time as this?”

Since I read this morning that Karen has chosen to silence herself permanently, I have decided to re-blog her work so that it doesn’t disappear forever.  I guess in this case “relief and deliverance will arise from another place” is the Hopegirl blog.