The Constitution of the World Health Organisation (WHO) was adopted by the International Health Conference conference held in New York from June 19th to July 22nd of 1946 and signed on July 22, 1946 by the representatives of 61 States (Countries) (Off. Rec. Wld Hlth Org., 2, 100). The Constitution came into force two years later on April 7, 1948 and so the WHO officially began. [1, 2]

Prior to this, the proposal to convene an international conference for the establishment of a new worldwide health organization originated at the 1945 San Francisco United Nations Conference on International Organization (which would become the United Nation).

Dr Szeming Sze, a prominent Chinese medical expert, who was educated at Cambridge, and worked in both UK and US, was instrumental in the creation of the WHO. His father, Dr. Alfred Sao-ke Sze (施肇基, Zhaoji Shi), was China’s ambassador to Great Britain, the first Chinese ambassador to the United States (1935) and at the end of WW1 signed treaties as the “President of the Chinese Republic” , he was a diplomat.

As China’s delegate, Dr Szeming Sze “conferred” with Dr. Karl Evang of Norway and Dr. Geraldo de Paula Souza of the Brazil, (the only other medical professionals in attendance) on creating an international health organization under the auspices of the new United Nations.

After failing to get a resolution passed on the subject, Alger Hiss, the secretary general of the conference, recommended using a declaration to establish an international conference on health, Sze and other delegates “lobbied” and the declaration was passed. Sze followed this through to WHO’s creating, but went to work for the United Nations, not the WHO, in 1954 [after CCP came to rule] he was appointed medical director of the United Nations! [3, 4]

The UN then held the International Health Organization conference from June 19 to July 22, 1946 at the Henry Hudson Hotel in New York city.  Prior to this, the Technical Preparatory Committee for the International Health Conference, met in Paris on February 15, 1946 to prepare for the conference and produced a draft constitution report.  This report was adopted on June 11, 1946 by the Economic and Social Council and then presented to the conference delegation from there it was signed into July 22, 1946.   The Conference’s technical committee suggested the name “World Health Organization”. [5]

Dr Sze’s electronic correspondence HERE

The Central Intelligence Agency (CIA) was created with the signing of the National Security Act on July 26, 1947 by President Harry S. Truman. [1, 2, 3] Aside from the purposeful unification of the three military departments, the act established the National Security Council. [4]

The CIA was established under the National Security Council (NSC) to be headed by a Director of Central Intelligence (DCI), who would be appointed by the President, and be their principal advisor for intelligence matters related to national security.

To “promote the national security by providing for a Secretary of Defence; for a National Military Establishment; for a Department of the Army, a Department of the Navy, and a Department of the Air Force; and for the coordination of the activities of the National Military Establishment with other departments and agencies of the Government concerned with national security.”

Although “modern U.S. intelligence can be traced back to World War II, with the establishment of the Office of Strategic Services (OSS)” in 1942 their “functions included the use of propaganda, subversion, and post-war planning” including running ‘Operation Paperclip‘.

In 2004 the Intelligence Reform and Terrorism Prevention Act which passed December 17, 2004, amended the 1947 National Security Act to provide for a Director of National Intelligence (DNI) who would assume some of the roles formerly fulfilled by the DCI. [1]

The DNI, supported by the Office of the Director of National Intelligence (ODNI), produces the President’s Daily Brief (PDB), a top-secret document including intelligence from all Intelligence Community (IC) agencies, handed each morning to the president of the United States – previously handled by CIA Director.

Freedom of Information requests and declassification has revealed  just how the CIA has helped “shape” history. “The CIA was vested with broad powers, functioning under minimal public scrutiny, often operating in international territories to counter perceived threats to U.S. interests,” and become involved in global affairs. [2]

On October 30, 1948 the first Randomised Controlled Trial (RCT) was conducted and published by the UK Medical Research Council in the British Medical Journal (BMJ) on “Streptomycin treatment of pulmonary tuberculosis“.  This was a “methodological landmark because it provided detailed information about the trial, and in particular, the steps taken to prevent foreknowledge of treatment assignments.”

This publication marks the birth of Randomised Controlled Trials the the gold standard for medical research. [1]

In the aftermath of WWII, the foundations of the North Atlantic Treaty Organization (NATO) were officially laid down on 4 April 1949 with 12 founding members signing of the North Atlantic Treaty in Washington DC, known as the Washington Treaty, “to provide collective security against the threat posed by the Soviet Union”.

“The Treaty derives its authority from Article 51 of the United Nations Charter, which reaffirms the inherent right of independent states to individual or collective defence.”

NATO is an intergovernmental military alliance between 28 European countries and 2 North American countries. [1]

Australia is not a member of NATO, (not North Atlantic), but are bound to the US by other intergovernmental treaties, so indirectly become involved in NATO defense activities:

• Australia, New Zealand, United States Security Treaty (ANZUS)
• AUSCANNZUKUS alliance
• Southeast Asia Treaty Organization (SEATO)

On April 12, 1955, Jonas Salk’s inactivated polio vaccine (IPV) was licensed in the US the same day “researchers announced the vaccine was safe and effective”.  It was hailed as “an historic victory over a dread disease…ushering in a new medical age”.  Between 1948 and 1955 several Polio (known officially as poliomyelitis) epidemics had occurred and people were fearful of the “disease”. [1, 4]

US physician Jonas Salk tested his experimental killed-virus vaccine on himself and his family in 1953. Then on “April 26, 1954, the Salk polio vaccine field trials, involving 1.8 million children, begin at the Franklin Sherman Elementary School in McLean, Virginia. Children in the United States, Canada and Finland participated in the trials, which used, for the first time, the now-standard double-blind method.” [2, 3]

Within days of Salk’s “inactivated” polio vaccine rolled out, cases began emerging across America of children who had become paralyzed in the limb that were injected with the new technology vaccine which had known live virus issues, and who’s mass produced formulations had not been tested in humans – The Cutter Incident.  Later forumulation problems also with Wyeth manufacturing (now Pfizer) but CDC covered this up.  [7] The polio case definition was then adjusted!

“The practice among doctors before 1954 was to diagnose all patients who experience even short-term paralysis (24 hours) with ‘polio'”. In 1955, the year the Salk vaccine was released, “the diagnostic criteria became more stringent”  that being “[i]f there was no residual paralysis 60 days after onset, the disease was not considered to be paralytic polio”, thus providing an immediate sharp decline in polio cases, even without a vaccine! [Page 230-33] Many things can cause transient paralysis.

According to the CDC “paralysis” dropped from 15,000 in the 1950’s to 100 cases in the 60’s. Since 1979, no cases of polio caused by wild poliovirus have originated in the U.S., but on July 21, 2022 a case was reported.

In 1961 the Salk vaccine was recalled due to live virus and presence of cancer causing SV40 monkey virus, and was replace with Albert Sabin’s oral polio vaccine, which also contained SV40. [6]

Prior to 1890 poliomyelitis was known through out history by hundreds of other names. By changing a disease name or case definition you can create or eliminate a disease or epidemic with the stroke of a pen. [5]

The US military research agency was created on February 7, 1958 by President Dwight D. Eisenhower in response to the Soviet launching of Sputnik 1 in 1957, and known as the Advanced Research Projects Agency (ARPA). Then in March 1972 organization first changed its name to DARPA (D for Defense), then changing back to ARPA in February 1993, then reverted to DARPA in March 1996. [1]

In 1999 DARPA’s primary mission “is to help maintain U.S. technological superiority and guard against unforeseen technological advances by potential adversaries” by pursuing “research and technology where risk and payoff are both very high and where success may provide dramatic advances for traditional military roles and missions and dual-use applications.” [2]

In June 2021 NIH head Dr Francis Collins et al stated a “DARPA-like culture at NIH can drive biomedical and health advances” as their vision for the March 15, 2022 established Advanced Research Projects Agency for Health (ARPA-H). [3, 4, 5]

In 1961 Sydney Brenner, Francois Jacob, and Matthew Meselson discovered that messenger RNA (mRNA) is the molecule that takes genetic information from DNA in the nucleus to the protein-making machinery (ribosomes) in the cell cytoplasm. Thus answered the question of how proteins were synthesised in cells. [1]

“A length of DNA that includes the “blueprint” for a single protein product is called a gene. Each three-nucleotide sequence [codon] carries the instructions for making a particular amino acid, with amino acids being the building blocks of proteins”.  In all, there are 20 amino acids which can be used to form a polypeptide chain, which when folds into a 3D shape it becomes a protein. [2, 3]

RNA is chemically similar to DNA except that:

• The sugar in its nucleotide building blocks is ribose and not deoxyribose
• RNA uses the nucleotide base uracil instead of thymine. But like thymine, uracil can pair with adenine
• RNA, especially mRNA, tends to be single-stranded, not double-stranded like DNA

Natural mRNA degredation is a precise, genetically controlled process with an approximate half-life of around 9 hours.  Around 40 proteins are produced/mRNA/hour. [5, 6, 7, 8]

In the COVID-19 gene-technology mRNA ‘vaccines’ the nucleotide uracil (uradine) has been replaced with pseudouradine, which causes the synthetic mRNA to last longer.  A study shows the synthetic mRNA can persist in lymph nodes for up to 60 days (possibly longer), constantly producing foreign spike protein! [4]

On October 10, 1962 President Kennedy signed the Drug Industry Act Amendments of 1962, also known as the Kefauver-Harris Amendments. This amendment now required drug manufacturers to supply efficacy data to the Food and Drug Administration (FDA), previously it was just safety data, for their product to be considered for licensing.  Intended to protect American consumers from “unsafe and ineffective drugs”. [1, 3]

In 1960 “Senator Estes Kefauver… decided that in dealing with medications, the government must do more than control their labels, contents, and safety and their marketing and distribution processes. It must also control their prices and enforce “competition….Although Kefauver’s main concern was pricing, another provision called for NDAs to show proof of both safety and efficacy.”  The thalidomide babies tragedies paved the way for the passing of the amendments, though the “pricing and patent-sharing provisions were deleted”. [2]

The amendment expanded the power of the FDA. “The task of proving efficacy is much more difficult, expensive, and time-consuming than the task of proving safety. To a great extent, efficacy, which is sensitive to individual conditions and mediated by market process, had in the past always been judged jointly by doctors and consumers…  In 1962, however, the FDA began to act on the premise that it could establish authoritative knowledge of efficacy prior to experience and experimentation in actual market processes….The time spent waiting for FDA approval and the expense and duration of the bureaucratically determined testing procedures combined to cause tremendous delays in drug development and production. Drug development declined significantly after 1962″ [2]

The FDA does no clinical testing, they rely solely on data selected and supplied by the drug manufacturer, called a ‘dossier’ [@16:50]

Before 1962 “controlled trials were still developing, and many marketed drugs were ineffective for their labeled uses.  Now, the standard for evidence is the well-controlled study, and the FDA’s implementation of the 1962 amendments contributed greatly to that.”[4]

The Drug Amendments also addressed the use of drugs in clinical trials, including a requirement of informed consent by subjects. [2]

Immune induced “efficacy” in vaccine trials was measured by the production of neutralising antibody titres – which assumed “protection” from “disease” – the symptom from said pathogen.

On January 10, 1963, Congressman Albert S. Herlong Jr. of Florida read into congressional record 45 “Current Communist Goals,” to overthrow the United States. “They were taken from the “The Naked Communist” by W. Cleon Skousen, who began his extensive study of Communism during his sixteen year term of service with the Federal Bureau of Investigation.   [1, 2, 3]

Communist Goal:
#15. Capture one or both of the political parties
#20. Inflitrate the press
#21. Gain control of key positions in radio, TV, and motion pictures

After 2020 election “it’s pretty clear these goals have been achieved” states Man in America

In 1966 the genetic code is cracked by Marshall Nirenberg, Har Khorana and Severo Ochoa by demonstrating that when the 4 possible nucleotide bases are sequenced in groups of 3 to form a codon, they encode one of 20 amino acids. In time codons which signal the start and end of protein synthesis are deciphered. [1]

Messenger RNA (mRNA) genetic sequence codes for a string of specific amino acids which form and fold into a specific protein within the cell cytoplasm.