Enabling statutes, regulations, executive orders, guidance documents and budget allocations.
Katherine Watt, Bailiwick News, May 2023
At least six Congressionally-authorized statutory frameworks and related budget appropriations, reinforced through Presidential Executive Orders and related executive branch declarations,[1] and implemented through hundreds of regulatory amendments,[2] mostly promulgated through the Federal Register since 1969, appear to have authorized and funded a coordinated US Government attack (actors), on the American people (targets), using toxic biological and chemical material (bioagents/biochemical weapons) distributed across state borders labelled as “Covid-19 vaccines.”[3]
These biochemical weapons have been fraudulently marketed by the US Government and pharmaceutical weapons manufacturers including Pfizer, Moderna, Johnson & Johnson and their manufacturing subcontractors as “safe and effective vaccines,” following the transfer of the US Government’s Chemical and Biological Warfare Program, formerly housed in the Department of Defense (DOD), to the Public Health Emergency (PHE) Emergency Use Authorization (EUA) Medical Countermeasures (MCM) program.
The American chemical and biological warfare program is now housed in the Department of Health and Human Services (HHS) and jointly operated by DOD, HHS, Department of Homeland Security, Department of State, most other federal agencies and their subordinate departments, divisions, offices, authorities, enterprises, committees, advisory boards and employees.
Six of the enabling statutes, in chronological order of Congressional enactment:
- 1969 – Title 50, War and National Defense, Chapter 32, §1511 et seq. Chemical and Biological Warfare, enacted Nov. 19, 1969 (PL 91-121).
- 1983 – Title 42, Public Health Service, §247d et seq. Public health emergencies, established July 13, 1983 (PL 98-49).
- 1986 – Title 42 – Public Health Service, §300aa-1 et seq. National Vaccine Program and Vaccine Injury Compensation Program, established Nov. 14, 1986 (PL 99-660).
- 1997 – Title 21 – Federal Food and Drugs Act, §360bbb et seq, Expanded access to unapproved therapies and diagnostics, adopted Nov. 21, 1997 (PL 105-115).
- 2002 – Title 42 – Public Health Service, §300hh et seq, National All-Hazards Preparedness for Public Health Emergencies, adopted June 12, 2002 PL 107-188).
- 2015 – Title 10 – Armed Forces, §4021 et seq., Research projects: transactions other than contracts and grants. Originally adopted July 29, 1958 (PL 85-568) for NASA, expanded for DOD use for “prototype” contracting on Nov. 25, 2015 (PL 114-92).