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911: Patent for Global COVID-19 Vaccine - Highly Deadly mRNA Platform
Emails sent between May 22, 2021 - May 29, 2021 notifying influential people and government officials that the COVID-19 mRNA INJECTIONS ARE BIOWEAPONS
Below is an example email of about 75 emails I sent between May 22, 2021 - May 29, 2021, notifying the MSM, alternative media, influencers, doctors’ organizations, senators, and governors that the COVID-19 mRNA INJECTIONS ARE BIOWEAPONS.
You may ask what compelled me to write this email and then incessantly call organizations and harass them as to why they were not covering the evidence I sent that could save millions of lives?
Brief answer: When I was reviewing the master patent, I discovered the lipid nanoparticle technology (which no one was informed that they were injected with) and came across a section that mentioned ‘triple helix DNA.’ The gravity of the implications of what these injections could do to our children and humanity hit me in that moment. I essentially went 72 hours without sleep in order to comprise the below email in the most effective and coherent way that I possibly could while pouring through hundreds of pages of horrifying government and clinical documents.
My key point is at the end of the email;
“These appear to be biological weapons that can only cause death and harm to millions around the globe. The Emergency Use Authorization for these biological agents in every country must cease immediately. There appears to be evidence that active participants, as defined as manufacturers, agents (including social media), CDC, NIH, FDA, HHS, spokespersons, marketers, et al. were acting upon their own willful malfeasant conduct in withholding scientific and clinical information as well as engaging in a manipulative propaganda campaign around the safety and efficacy of these biological agents.”
My prayers and intentions were that those who received my emails in May of 2021 would verify the information I sent and immediately share the message that the COVID-19 mRNA VACCINES ARE BIOWEAPONS using an advanced lipid nanoparticle technology made in China.
Unfortunately my intentions were not the same as those who initially received my message or that I reached out to, at that time. I was told that my idea about educating the masses that the shots are bioweapons and need to be stopped immediately was not a ‘good idea’. That the narrative had to emphasize "‘choice.” With some exceptions, the alternative media’s focus began to primarily shift to individuals having a ‘choice to be injected’ while MSM moved full-steam ahead pushing the deadly shots.
As fate would have it, I ended up being the messenger of my research. I am deeply grateful to Doug Billings, Stew Peters, Ann VanderSteel, and Brannon Howse who were courageous enough to have me share the TRUTH despite how terrifying it was, and even though it was from a messenger who did not have the credentials of an MD, PhD, or JD.
Disclaimer: I am not an mRNA expert, scientist, or doctor. I put the email summary together to the best of my ability after reading thousands of pages of scientific, legal, and government documents. Due to the VAERS data and reports on myocarditis, pulmonary failure and miscarriages, and after reviewing the master MODERNA mRNA patent, I hypothesized that chemotherapy agents could potentially be in the injections. There has been no evidence to prove this hypothesis to be true. However, there is an overwhelming body of evidence that the mRNA spike proteins and PEGylated LNPs induce these horrifying life-threatening and deadly effects and many others.
The Kingston Report. TRUTH WINS.
From: Karen Kingston <*kingston@*****.com>
Date: Thursday, May 27, 2021 at 8:02 PM
To: "Wendy.****@foxnews.com" <Wendy.***@foxnews.com>
Subject: 911: Patent for Global COVID-19 Vaccine - Highly Deadly mRNA Platform
Hi Wendy, I’m a consultant in the Pharma and Med Device industry. I conduct analysis of clinical data, IP landscape/patents, federal regulations, and communication trends and then develop content and strategic plans to influence how physicians manage various disease states, as well as what to communicate to the consumer population. My clients have included Pfizer, Johnson & Johnson, Medtronic, Allergan, et al.
I’m hoping you can pass the information I gathered regarding the COVID-19 biological agents onto a team at FOX and FOX can help in the efforts against the false propaganda regarding the COVID-19 injections. Many people are putting themselves and their children at unwarranted risk for harm, frequently resulting in permanent disabilities or death.
Most important, the attachment labeled SM-102 Patent is the global patent for the mRNA lipid nanoparticle (LNP) vaccines granted by WIPO to Moderna on August 6, 2020.
Please have an expert in auto-immune disease medical research review this patent and the ones linked in this email. I believe they will conclude that the COVID-19 injections are bioweapons that contain gain of function (GOF) chimeric viruses and toxins under the guise of mRNA therapeutic vaccines combined with a ‘diagnostic/therapeutic’ lipid nanoparticle (LNP) platform. Per the patent, the LNP can target specifics organs and systems throughout the body, including, but not limited to reproductive, cardiovascular, pulmonary, and the central nervous system, specifically crossing the blood brain barrier.
I apologize in advance for the ‘drinking from a firehose’ data in this e-mail.
Americans Right to Informed Consent
The FDA, CDC, NIH, and most Medical Associations, such as the American Academy of Pediatrics, are guilty of dozens of violations under the FD&C Act, by withholding or lying about these biological agents, including the dangers and risks of “COVID-19 Vaccines” under informed consent, per Sec. 564 of the FD&C Act:
Every communication (written, news, videos, social media, websites, podcasts, etc.) about the Covid-19 ‘vaccines’ must clearly state that:
The ‘vaccines’ are not approved by the FDA for the prevention or treatment of COVID-19, but are under Emergency Use Authorization (EUA) only
The ‘vaccines’ have NOT been proven to be safe or effective in stopping the infection or transmission of the SARS-CoV-2, the virus that causes COVID-19
Every patient has the right to be informed of the benefits and risks of the ‘vaccine’, including all reported side effects, other treatments available, and the right to refuse treatment
Following is a snippet of the information I’ve researched:
COVID-19 Vaccines Patents are based on Research from China
In Jan of 2017, MIT, Harvard, et al. filed a patent for Vaccine Nanotechnology. https://pubchem.ncbi.nlm.nih.gov/patent/US-9539210-B2 Under the Section STATEMENT OF GOVERNMENT SUPPORT – it clearly states that the invention was made possible by grants from the NIH and is entitled to rights of the invention. This patent dates back to a provisional filed Oct. 12, 2007 Ser. No. 60/979,596 which also stats the NIH’s ownership in the vaccine nanotechnology platforms.
In December of 2017, the NIH lifted its restrictions on Gain of Function (GOF) research. (attached – Dec 2017 NIH GOF).
In February of 2018, the USPTO granted the University of North Carolina a patent for Chimeric Coronavirus Spike Protein(s). The patent covered GOF spike coronaviruses from SARS-Cov-1, MERS, and bat coronaviruses. The NIH’s ownership is stated in this patent as well. In 2005, a NIH/People’s Republic of China funded study was published on chimeric research with bat coronaviruses. Ref 29 – Thanks the NIH for their grant for this research.
ref 29 This work was jointly funded by a special grant for “Animal Reservoir of SARS-CoV,” State Key Program for Basic Research Grant 2005CB523004, and State High Technology Development Program grant no. 2005AA219070 from the Ministry of Science and Technology, People's Republic of China; the Sixth Framework Program “EPISARS” from the European Commission (no. 51163); the Australian Biosecurity Cooperative Research Centre for Emerging Infectious Disease (Project 1.007R); and an NIH/NSF “Ecology of Infectious Diseases” award (no. R01-TW05869) from the John E. Fogarty International Center and the V. Kann Rasmussen Foundation. For the full-length genome sequence of SL-CoV Rp3, see GenBank accession no. DQ71615. Additional GenBank accession numbers are given in the supporting material.
It's noteworthy that in 2004, the NIH also collaborated with China on chimeric gain of function research of coronavirus with HIV-1 and SIV (Simian (aka monkeys) Immunodeficiency Viruses)
In January of 2021, researchers published an article noting 4 insertions of HIV-1 gp120 spike protein and the HIV-Gag in the SARS-CoV-2 spike protein. Attached is a copy of the withdrawn publication. (see attached Spike_Hiv)
HIV gp120 is a glycoprotein that is part of the outer layer of HIV. It is essential for viral infection and HIV entry into CD4+ cells and their depletion. https://pubmed.ncbi.nlm.nih.gov/20088758/
Gag polyprotein is the main structural protein of HIV-1 and other retroviruses*. A tech enthusiast may refer to Gag as the ‘operating system’ of a retrovirus because it forms higher ordered structures required for the correct assembly, budding, and maturation of new infectious particles. https://pubmed.ncbi.nlm.nih.gov/23266279/
*Retroviruses are RNA viruses that insert a DNA copy into the genome for viral replication.
Note: Researchers may want to test the COVID-19 biological agents for these HIV-1 proteins, as well as the blood of some subjects who were injected, 3- and 6- months post second injections, including children. Cardiovascular and thrombolytic events are becoming highly frequent among a children and teens per local news stories. https://alethonews.com/2021/05/26/at-least-18-teens-and-young-adults-hospitalized-in-connecticut-with-myocarditis-after-covid-vaccines/
U.S. COVID-19 Vaccines are Being Manufactured in China, Chinese Companies Making Large Profits
A company called SINOPEG, based in China, is the manufacturer of PEG for ALL mRNA vaccines that contain PEG, including Pfizer and Moderna. It’s important to note that these proprietary components found in the COVID-19 injections have Material Safety Data Sheets (MSDS) which are used for chemicals, metals, industrial lubricants and toxins. As noted on the SINOPEG site, they are not fit for human consumption.
The SINOPEG COVID-19 PEG portfolio can be found here. https://www.sinopeg.com/covid-19-vaccine-excipients_c138
Ingredients for US vaccines can be found here https://portal.ct.gov/Coronavirus/Covid-19-Knowledge-Base/Vaccine-Ingredients
The “Pfizer vaccine” was not developed by Pfizer. In June of 2018, Pfizer entered into a royalty agreement with BioNTech to manufacture the mRNA vaccine. Aside from the $50 million upfront payment to BioNTech, the royalty agreement was contingent on the production and sale of an mRNA LNP vaccine under Emergency Use Authorization in response to a global pandemic.
See Sec 3.1 Payments
BioNTech is also sharing the profits from the “Pfizer vaccine” with another company in China, Fosun Pharma, who is also a manufacturer of the “Pfizer vaccine.” Pfizer was guaranteed an order of a minimum of 1 Billion injections and up to 2 Billion injections for this year. See Slide 8 Biontech Investor Presentation. https://investors.biontech.de/static-files/82c9e451-7503-4217-a51f-ee7fb6497b17?fbclid=IwAR2MRfUtXExUeDS4qiqbk6jnRay-k0fp74ZKeBlGobChqyLAcqToU2uxm7Q
US COVID-19 ‘Vaccine’ Trials Are Being Conducted in Foreign Countries - Global COVID-19 ‘Vaccine’ Studies are Being Conducted in China
On August 26, 2020, the CDC released a list of global COVID-19 trials. 9 of the trials are being conducted in CHINA. https://www.cdc.gov/vaccines/acip/meetings/downloads/slides-2020-08/COVID-07-Oliver.pdf
Although there are four COVID-19 therapies listed under “US Trials,” if you read the FDA EUA Review Memorandums for Pfizer, you’ll notice that these studies are multi-national studies. The majority of patients and investigators are outside the US.
Pfizer Studies Centers: US, Argentina, Brazil, Germany, South Africa, Turkey.
Global Moderna mRNA Patent is for Therapeutics and Diagnostics – This is the Global Vaccine Patent
On August 6, 2020 Moderna was granted an international patent for Lipid Nanoparticle Technology (LNP) for therapeutic and diagnostic uses, including LNP encapsulated mRNA technologies. (see attached SM-102 Patent, page 1).
It’s important to note that in the US, diagnostics are categorized as medical devices by the FDA.
Although over 100 million Americans may have been injected with a medical device technology, if they were, none were given informed consent.
These vaccines are “NOT APPROVED BY THE FDA”, therefore under TITLE 21 of the FD&C Act, Sec. 814.9: Confidentiality of data and information of pre-market approval (PMA) of medical devices, states;
(b) The existence of a PMA file may not be disclosed by FDA before an approval order is issued to the applicant unless it previously has been publicly disclosed or acknowledged.
May 25, 2021 - FDA Approves Modifications to COVID-19 Boosters Without Notifying the Public
The FDA also updated COVID-19 Manufacturer Guidelines authorizing modifications to the COVID-19 booster shots without having to notify the public.
Under the Preface of the below FDA document, it states that the guidelines for modifications to the booster vaccines are effective immediately and that it’s not practical to inform the public.
Page 2 also notes that “healthy people will be injected and that the injections have the potential for 'broad use' under the EUA.” – Again, no need to inform the public of these modifications or ‘broad uses’.
“HIGHLIGHTS” of Moderna/NIH SM-102 Patent
Vaccines May Include Chemicals, Viral Proteins (i.e. HIV Gag), Toxins, and Drugs That Can Lead to Infertility, Cancer, Biocorona, Psychosis, et al.
At the end of this email, I copied and pasted some of the ingredients from the patent, including lithium salt, lithium chloride, cellulose acetate, chemotherapies, genetic materials, genetic proteins, cytokines, metals and other dangerous substances, some psychotropic.
One of the chemotherapies mentioned in the patent is trastuzumab, a chemotherapy product made by Pfizer. http://labeling.pfizer.com/ShowLabeling.aspx?id=12725 Below is an excerpt from the trastuzumab prescribing information.
WARNING: CARDIOMYOPATHY, INFUSION REACTIONS, EMBRYO-FETAL TOXICITY, and PULMONARY TOXICITY
Cardiomyopathy: Trastuzumab products can result in subclinical and clinical cardiac failure manifesting as CHF, and decreased LVEF, with greatest risk when administered concurrently with anthracyclines. Evaluate cardiac function prior to and during treatment. Discontinue TRAZIMERA for cardiomyopathy. (2.3, 5.1)
Embryo-Fetal Toxicity: Exposure to trastuzumab products during pregnancy can result in oligohydramnios, in some cases complicated by pulmonary hypoplasia and neonatal death. Advise patients of these risks and the need for effective contraception. (5.3, 8.1, 8.3)
Is trastuzumab the reason why healthy children and teenagers injected with Pfizer vaccine are suffering from cardiac events such as pericarditis and cardiac arrest? https://www.nbcconnecticut.com/news/coronavirus/covid-vaccine/mom-of-conn-teen-speaks-after-son-suffers-heart-condition-days-after-covid-19-vaccine/2495057/
Is trastuzumab the reason why the side effect profile for Moderna injections looks like someone who has undergone gone chemotherapy? In the Phase 3 Moderna Trials submitted to the FDA, per page 37 of the EUA, 82% of subject who received 2 doses of the Moderna biological injections had Grade 3 or 4 Systemic Side Effects. The FDA Defines Clinical Adverse Events as follows, FDA Presentation Slide 14:
Grade 3: Severe or medically significant but not immediately life threatening, hospitalization or prolonged hospitalization
Grade 4: Life-threatening consequences, urgent intervention indicated
Grade 5: Death
Is trastuzumab the reason why Phase 1 inclusion protocols looks similar to those of chemotherapy or HIV studies?
Two forms of sexual protection need to be used if a male subject is intimate with a woman (a woman who’s not in the study). She also must meet with a safety advisor. If she’s impregnated she must report it (again - she is not in the study), and male subjects must reportif they touch or are in close contact with a pregnant woman. See Sec 10.4.1 Male Participants Reproductive Inclusion Criteria
Women can NOT participate in the Pfizer study if they are of Child Bearing Potential. See Sec. 10.4.2
Furthermore, females are warned not to be exposed to the Pfizer ‘vaccine’ while breastfeeding or be exposed to anyone who was in the study. See Sec. 126.96.36.199 Exposure During Breastfeeding
Could the Pfizer biological injection include their chemotherapy trastuzumab? Or be spiked with the HIV proteins?
Are the ‘Vaccines’ a Biological Medical Device and Technology Platform?
If the public is in disbelief that they may have been injected with a smart technology, they may be interested in learning that Elon Musk/TESLA just joined the COVID-19 'vaccine' market per the May 12, 2021 article in NATURE, a highly regarded scientific, peer-reviewed journal. https://www.nature.com/articles/s41587-021-00912-9.pdf?fbclid=IwAR1xNdAetLM4ZzmTSH9gdvscml6S7AJ4ijl4-J9GiAwXof4dyZCdEY7ozcU
Of note, per the COVID-19 Patent Landscape visual from the article, it appears all manufacturers will need to pay some royalty to the NIH in the mRNA and theranostic (therapeutic/diagnostic). This is likely related to the 2017 Nanotechnology Patent https://pubchem.ncbi.nlm.nih.gov/patent/US-9539210-B2 and 2018 chimeric mRNA patent
Concerns of FDA panel members were safety in pregnant woman, safety and need in children under the age of 18, and verbatim from the FDA memo ‘FDA pointed out that vaccine development has a long history and FDA is not aware of an example of any vaccine that is effective against mild disease that is not also effective against severe disease.’
In regards to the children, at least 8 have had a cardiac or thrombolytic event from the Pfizer Phase 3 study group of approximately 2,000 children aged 12-15. According to the American Heart Association, the risk for this age group is only 5/100,000.
The biological agents being distributed by Pfizer, Johnson & Johnson, and Moderna are not vaccines. Per their own FDA filings and the FDA authorization letters, these injections DO NOT prevent infection or transmission of SARS-Cov-2, but only allegedly reduce the risk for symptoms of an ambiguously defined ‘disease’ called COVID-19, which most adults have a 99.9% chance of surviving and children have a 99.998% chance of surviving. For children specifically, it is statistically and clinically impossible to make a vaccine for children that is more effective or safe than their own innate immune response to SARS-CoV-2 and its variants.
These appear to be biological weapons that can only cause death and harm to millions around the globe. The Emergency Use Authorization for these biological agents in every country must cease immediately. There appears to be evidence that active participants, as defined as manufacturers, agents (including social media), CDC, NIH, FDA, HHS, spokespersons, marketers, et al. were acting upon their own willful malfeasant conduct in withholding scientific and clinical information as well as engaging in a manipulative propaganda campaign around the safety and efficacy of these biological agents.
I have much more evidence and references for these statements and more from FDA.gov, CDC site, HHS, PubMed, PubChem, SEC Filings, et al. I can provide a timeline dating back to 2004 through today on how much of this happened. I have the clinical and technology data for J&J as well in there is any interest in additional information regarding this concerning matter.
With respect and appreciation for the integrity and courage of the FOX News Team– Karen Kingston
- The Kingston Report. TRUTH WINS.
Page 149 – May include trastuzumab.  In some embodiments, the lipid nanoparticles described herein may be used therapeutically. For example, an mRNA included in a LNP may encode a therapeutic polypeptide (e.g., in a translatable region) and produce the therapeutic polypeptide upon contacting and/or entry (e.g., transfection) into a cell. In other embodiments, an mRNAincluded in a LNP may encode a polypeptide that may improve or increase the immunity of a subject. In some embodiments, an mRNA may encode a granulocyte-colony stimulating factor or trastuzumab.