Weaponization of Language and Law: US Government Bioterrorism Program from 1969 to Covid
Excellent new reporting:
Jan. 13, 2022 - Funding the Control Grid Part 1: The Biomedical Framework, by The Sharp Edge at Corey’s Digs. Detailed breakdown of Congressional authorization and funding for present and future bioterrorism programs in the 2023 NDAA and 2023 Consolidated Appropriations Act.
Jan. 13, 2022 - Anatomy of the sinister Covid Project, Part 1, by Paula Jardine at The Conservative Woman. Deep dive into
biodefensebioterrorism program history and Robert Kadlec’s role.
Below is an abstract written for organizers of an international human rights law conference to which I’ve been invited. The full paper is due by mid-May and the conference will be held in June.
Writing the abstract and responding to a comment at my Gab feed, helped me further distill the language and classification substitutions (lies) that keep people confused about the genocide and illegal war we’re living and dying through.
The commenter asked, “Can we find out if the DOD asked permission to experiment on us?” and linked to 50 U.S. Code § 1520a - Restrictions on use of human subjects for testing of chemical or biological agents.
Under the illegitimate pseudo-law frameworks set up to pseudo-legalize an unjust war on the world’s people and pseudo-legalize the actions of men and women committing war crimes, No. Injection recipients never had to be asked for permission to “experiment on us.”
It’s not an experiment.
It’s an attack.
The recipients of Covid-19 bioweapons, and now all products classified as ‘vaccines,’ are not patients or subjects in clinical research trials.
The recipients of Covid-19 bioweapons are military targets.
The US Government is not testing novel, investigational medicinal treatments to protect or cure people.
The US Government is using intentionally lethal weapons to injure and kill people.
Military officers don't ask targets for permission to use weapons to injure and kill the targets.
Military officers follow orders from superior officers, up to the Commander-in-Chief, the US President, to use weapons to injure and kill targets.
The products are not a class of medicinal treatments administered to protect the recipients from infectious disease (the former meaning of ‘vaccines.’)
The products are a class of bioweapons administered to protect the US Government, its central bank owners, and its land and resources, from their enemy: healthy, living men, women and children.
The pharmaceutical companies researching, developing and manufacturing Covid-19 bioweapons are not private business companies led by private business executives, with commercial interests in, or regulatory supervision of, product safety and consumer protection.
The pharmaceutical companies researching, developing and manufacturing Covid-19 bioweapons, under federal military contracts, are federalized defense production facilities, operated by commissioned executives, working under the control and on behalf of the US Government’s military-industrial-pharmaceutical complex, to produce bioweapons designed, intended and highly effective for injuring and killing recipients.
The nurses and doctors and pharmacists and firefighters injecting people are not private medical or health care workers with professional ethical obligations under biomedical ethics laws, codes and conventions.
Nurses, pharmacists and other ‘vaccinators’ have been conscripted into the US Department of Defense military-industrial-pharmaceutical complex, as commissioned, reserve or volunteer corps officers of the US Public Health Service, which is a military branch, to carry out military orders at “point of dispensing” to injure and kill the target population: living men, women and children.
The whole biowarfare program, aimed at all of humanity, by those who would like to kill off most of the world’s people and set themselves up as gods and overlords of the remnant, has been hiding in plain sight for decades.
Weaponization of Language and Law: US Government Bioterrorism Program from 1969 to Covid.
ABSTRACT: This paper addresses provisions of American law that enabled the US Government, Department of Defense, Department of Health and Human Services, pharmaceutical contractors, United Nations World Health Organization, World Economic Forum, member states and private research and development funding organizations such as the Bill and Melinda Gates Foundation, to jointly develop and deploy bioweapons on target populations around the world.
These American laws also set up structural barriers to legal accountability, to delay public understanding of the criminal enterprise and impede substantive criminal and civil prosecutions, and have been replicated in the federal laws of other countries.
The US Government bioterrorism program includes development and deployment of strains of communicable pathogens, aerosolized toxins, and products allegedly intended to prevent or treat effects of infection and exposure in human beings. Examples include swine influenza, avian influenza, human immunodeficiency virus (HIV), acquired immune deficiency syndrome (AIDS), anthrax, squalene, pyridostigmine bromide, Gulf War Syndrome, severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), Coronavirus Disease-2019 (CoViD-19), lipid nanotechnology, genetic coding platforms and other chemical, biological, radiological and nuclear materials.
The bioterrorism programs violate the 1975 UN Convention on the Prohibition of the Development, Production and Stockpiling of Bacteriological (Biological) and Toxin Weapons and on their Destruction; the 1990 US Biological Weapons Antiterrorism Act, codified at 18 USC 175; the 1997 UN Convention on the Prohibition of the Development, Production, Stockpiling and Use of Chemical Weapons; the 1998 US Chemical Weapons Convention Implementation Act codified at 18 USC 229 and 22 USC 6701; and related American and international law.
But the illegal and malign offensive attack on the world's population has not yet been stopped by governments, because the bioterrorism program has been misclassified as a lawful and defensive public health program mounted by those same governments in response to a Public Health Emergency of International Concern (PHEIC), using linguistic redefinition of terms in conjunction with the legal frameworks created by the WHO International Health Regulations, including amendments adopted in 2005, and implemented by participating nation-states and their political subdivisions.
Through gradual, covert statutory reclassification and program transfers, reinforced through Presidential Executive Orders and related executive branch declarations, and implemented through hundreds of regulatory amendments, the US Government's Chemical and Biological Warfare Program originally housed in the Department of Defense (DOD), became the Public Health Emergency-Emergency Use Authorization-Medical Countermeasures program housed in the Department of Health and Human Services (HHS).
The bioterrorism program is now jointly operated by DOD, HHS, Department of Homeland Security, Department of State, most other US federal agencies and their subordinate departments, divisions, offices, authorities, enterprises, committees, advisory boards and employees, in collaboration with the World Health Organization, the Bill and Melinda Gates Foundation, and other public, private and public-private hybrid institutions around the world.