Pre-Pandemic Timeline
2000 – 2015
Chronological order of significant global, Australian and SA data points leading up to the COVID-19 Pandemic.
Navigate the timeline pages:
1800s | 1900-1945 | 1946-1979 | 1980-1999 | You Are Here | 2016-2018 | 2019 | 2020 | 2021 | 2022 | 2023
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Data points are continuously being added so please come back again soon
Vaccine Confidence Project (to measure and track public trust) is funded by BMGF
- Around June 2023 Heidi Larson launched a new initiative called the Global Listening Project (GLP) to improve public trust in crisis preparedness.
DNA: Its “purpose” and susceptibility may be different than what we’ve been taught
A paper published in Int. J. of Radiation Biology called “DNA is a fractal antenna in electromagnetic fields”, concludes that “DNA appears to possess the two structural characteristics of fractal antennas, electronic conduction and self symmetry. These properties contribute to greater reactivity of DNA with EMF in the environment, and the DNA damage could account for increases”…in adverse health outcomes such as cancer.
Science is still figuring out the complexities of our genetic material and the role it plays in life and health, and to introduce a brand new gene-based technology referred to as a “vaccine” on the global population (2021), at the same time as rolling out 5G towers is alarming.
UN PrepCom 2 marks beginning of the Sustainable Development Goals
The United Nations Committee on Sustainable Development (UNCSD) hold their second session of the Preparatory Committee (PrepCom 2) at UN HQ in New York on March 7-8, 2011. This meeting marks the begining of the Zero Draft version of “The Future We Want” report which forms the basis for the the 2015 Sustainable Development Goals, along with “the scope of a green economy” which is adopted in the June 2012 second Earth Summit. [1, 2, 3, 4,]
Foundation for Vaccine Research is launched
As a progression from “It’s Time Campaign”, 14 scientists, led by Peter Hale, together with “advocacy experts” launch the Foundation for Vaccine Research incorporated in Washington DC on June 1, 2011. The aim of the foundation is “to create global awareness for the need for increased, flexible, long-term funding for vaccine research”. [1, 2]
CDC: Advanced Molecular Detection (AMD) initiative needed to remain an international leader
Following a June 15, 2011 Future Strategies for Bioinformatics in CDC’s Infectious Diseases Laboratories intenal report which identified a “critical need” for increased Advanced Molecular Detection (AMD) capacity at the CDC. Concluding “[t]he authoritative analysis and interpretation of scientific data is a critical area where CDC must excel for the Agency to continue to provide international leadership in public health and policy. The mission of CDC will be seriously compromised if the organization does not have the appropriate bioinformatics expertise and computational infrastructure.” Among other things “Should this occur, CDC will be at risk of going from outdated, to obsolete, and then to irrelevant”
President Obama’s 2014 budget gave life to CDC’s AMD initiative, which may have been motivated with the threat of an” emerging variety of highly antibiotic-resistant bacteria” called superbugs!
Using next-generation sequencing technology to identify complete genetic sequences of microorganisms, the CDC aimed to user a “new era for controlling infectious threats” and “revolutionizing” its “ability to diagnose infectious diseases, investigate and control outbreaks, understand transmission patterns, develop and target vaccines, and determine antimicrobial resistance—all with increased timeliness and accuracy and decreased costs”. [1]
CDC claim “each year the flu costs businesses approximately $10.4 billion in direct costs for hospitalizations and outpatient visits for adults.” CDCs intention is to detect patterns more precisely in order to make better vaccines!
Fast forward November 2020 and AMD becomes the precursor to CDC’s NS3 and SPHERES SARS-CoV-2 genetic sequencing efforts. [It’s as though they knew the virus would mutate and accelerate variants after vaccine rollout!]
NIH funded the Single Cell Analysis Project (SCAP)
NIH launched the Single Cell Analysis Project (SCAP), a 5 year Common Fund program aimed to:
- Improve our understanding of cell heterogeneity, including defining cell types and dynamic cell states.
- Accelerate the development of new innovative tools and approaches fore cell analysis.
- Accelerate the validation, translation, and adoption of new technologies.
- Engage multidisciplinary teams and attract new approaches and researchers to the field.
Laying the foundation for the future global medical progression. [1]
Grant funding was awarded for such projects that encourage the development of “next-generation, innovative technologies to better define cell heterogeneity in situ.” The techniques were to “provide new analytical measures and manipulations of cellular contents, structure and activity significantly beyond those currently available at the single cell level.”
IOM: vaccine injury review – “the evidence is inadequate”
On September 25, 2008 a committee of experts met, who were convened by the Institute of Medicine (IOM) to review “the epidemiological, clinical, and biological evidence regarding adverse health events associated with specific vaccines covered by the Vaccine Injury Compensation Program.”
Three years later, in a press release on August 25, 2011, they stated “[a]n analysis of more than 1,000 research articles concluded that few health problems are caused by or clearly associated with vaccines.” Also they state “that while no vaccine is 100 percent safe, very few adverse events are shown to be caused by vaccines“. Their report “Adverse Effects of Vaccines” was published 2012. [Inadaquate evidence!]
A key component of the 1986 National Childhood Vaccine Injury Act required the U.S. HHS to collaborate with the Institute of Medicine to assess the safety of vaccines and potential adverse events, especially in children.
The National Academy of Sciences web page specifically states “the MMR vaccine is not associated with autism or childhood diabetes”, but there are many more vaccines than just MMR.
The IOM review found that “the evidence is inadequate to accept or reject a causal relationship between [DTaP] vaccine and autism.” So when the CDC states there is “no evidence” that [all] vaccines cause autism [4] – they are correct, and through FOIA the CDC can produce NO evidence! [1, @27:30 2].
Also the one DTaP study which happened to “suggest an association between serious neurological disorders and whole-cell pertussis immunization” was “rejected” from the review as it “lacked an unvaccinated comparison population.”!
In 2023, Kathleen Stratton, a NASEM official AGAIN leads a panel of experts to assess, this time, the COVID-19 vaccine specific injury. [3]
Genome sequencing is now cheap and fast
On September 16, 2011, Richard Resnick in his TED talk revealed that genome sequencing is now so cheap and fast it will open up opportunities for personalised genome sequencing for health care, insurance and politics!
“Now what we do is we take a genome, we make maybe 50 copies of it, we cut all those copies up into little 50-base reads, and then we sequence them, massively parallel. And then we bring that into software, and we reassemble it, and we tell you what the story is.”
The Human Genome Project sequenced 3 gigabases which took 15 years, now one run on a modern machine can process 200 gigabases in a week, and that capacity is increasing and now the price of sequencing a base has fallen 100 million times!
With a world wide capacity to sequence human genomes is 50-100 thousand per year, in 2011 and the one lab that represents 20% of all the global capacity is the Bejing Genomics Institute (BGI) in China.
[BGI provided 10 million COVID-19 PCR test kits to Australia. It is known that the Chinese are building a DNA profiling database for genomic surveillance, which is of great concern for Australians.]
There is still much to learn about the human genome and genetic material. In March 2022 the first complete, gapless sequence of a human genome revealed there are hidden regions! “These unresolved regions include segmental duplications, ribosomal rRNA gene arrays, and satellite arrays that harbor unexplored variation of unknown consequence” [1]
Global population reaches 7 billion
On October 31, 2011, top United Nations officials marked the global population reaching 7 billion with a call to action to world leaders to meet the challenges that a growing population poses.
The “implications of the new milestone for sustainability, urbanization and migration in a world where conflicts and weather disasters are driving people from their homes and climate change is exacerbating food and water shortages” provide “opportunities” to take action.
UN Secretary-General Ban Ki-moon “noted that the world’s population reached 6 billion in 1998, only 13 years ago, and it is expected to grow to 9 billion by the middle of this century, or even a few years earlier – by 2043.” According to the latest UN figures… the global population would “surge past 9 billion before 2050” and pass 10 billion by 2100 if current fertility rates continue at expected levels.”
With climate change allegedly linked to increased disease epidemics and population growth this is a significant milestone.
Global Climate and Health Alliance, an NGO, is formed
On December 4, 2011, during the 17th Conference of the Parties (COP17) of the United Nations Framework Convention on Climate Change (UNFCCC), the first Global Climate and Health Summit was held and the Global Climate and Health Alliance, an NGO, is formed. [1, 2]
Alliance members meet annually at the conference of the UN Framework Convention on Climate Change – they believe “The climate crisis is a health crisis“
International Consortium for future pandemics is launched
The International Severe Acute Respiratory Infection Consortium (ISARIC) was launched on December 16, 2011, and is a group of international organisations taking part in a new global consortium organized to prepare clinical research for future influenza pandemics or other rapidly emerging public health threats.
Infectious outbreaks are not limited only to influenza outbreaks but are global phenomena that are occurring with increasing frequency.
The standardized and open-access protocols developed during this consortium will allow researchers from all participating countries to work with, adapt and evolve common clinical case ascertainment. This will ensure that high-quality and comparable clinical research is practiced on a global scale.
As part of The Global Health Network (TGHN) also funded by the Bill & Melinda Gates Foundation, ISARIC has “an overreaching ambition to change the way in which research is carried out during and between epidemics, ISARIC aims to address the social and ethical issues related to this paradigm change.”
The ISARIC is being launched by the Wellcome Trust, and the UK Medical Research Council, the Bill & Melinda Gates Foundation, Inserm, Li Ka Shing Oxford Global Health Programme and the Singapore Ministry of Health.
Chinese miners fall ill after shoveling bat faeces
Sometime in 2012 in Yunnan province, China, 6 miners become seriously ill with respiratory symptoms after shovelling bat faeces at the bottom of a mine shaft. The miner’s respiratory virus (RaBtCoV/4991) was said to came from rufous horseshoe bats.
The mineshaft floor was covered with a fungus. “Although the fungus turned out to be the pathogen that had sickened the miners” Shi speculated “it would only have been a matter of time before they caught the coronaviruses if the mine had not been promptly shut.”
“Shi’s team had been called in to investigate the virus profile of a mineshaft in Yunnan’s mountainous Mojiang County—famous for its fermented Pu’er tea—where six miners suffered from pneumonia-like diseases (two of them died). After sampling the cave for a year the researchers discovered a diverse group of coronaviruses in six bat species. In many cases, multiple viral strains had infected a single animal, turning it into a flying factory of new viruses.” [2]
Since 2013 the Wuhan Institute of Virology has been experimenting with these bat coronaviruses, including their use in 2015 controversial gain-of-function study.
In February 3, 2020, Shi Zhengli et al published paper suggesting SARS-CoV-2 genome was almost 80% identical to that of SARS-CoV, the virus that caused SARS in 2002, but it was 96.2% similar to RaTG13 another genome from Yunnan bat caves. [1]
Highly pathogenic Influenza virus research voluntarily paused, Fauci argues for it.
On January 27, 2012 it was published that the influenza virus research community implemented a 60-day voluntary moratorium on “gain-of-function” experiments related to “highly pathogenic avian influenza H5N1 viruses leading to the generation of viruses that are more transmissible in mammals.”
On October 9, 2012 Anthony Fauci, director of NIAID, and as a key funder of Influenza research, publishes “The Way Forward” for this kind of gain-of-function research. [1]
Fauci wrote “the benefits of such experiments and the resulting knowledge outweigh the risks. It is more likely that a pandemic would occur in nature, and the need to stay ahead of such a threat is a primary reason for performing an experiment that might appear to be risky.”
The Davos Global Risk Forum sponsors the first One Health Summit
February 19-22, 2012, the first One Health Summit was held in Davos, Switzerland sponsored by the private membership entity called the Global Risk Forum. [1, 2]
The Summit presented the One Health concept as a way to manage health threats, focusing on food safety and security. The conference ended by approving the “Davos One Health Action Plan,” which pinpointed ways to improve public health through multi-sectoral and multi-stakeholder cooperation. [3]
“Many emerging health issues are linked to increasing contact between humans and animals, the industrialization of food production, and environmental pollution. Global change has created new threats to the health of both animals and humans…[associated with the] systemic interconnections of human, animal and environmental health….Being a global movement at the interface of science, society, policy and practice, One Health is, therefore, also deeply interdisciplinary and cross-sectorial.”
Global Vaccine Safety: Blueprint, Plan and Initiative
In 2011 the WHO and a group of partners developed a strategic document on vaccine safety called the Global Vaccine Safety Blueprint (GVSB) published February 22, 2012. The Blueprint proposes a strategic plan for strengthening vaccine safety activities globally. It focuses on building national capacity for vaccine safety in the world’s poorest countries through the coordinated efforts of major stakeholders. [1, 4]
Three months after the GVS Blueprint was published 94 Member States at the 65th World Health Assembly endorsed the Global Vaccine Action Plan (GVAP) serving as a framework to guide immunization efforts through to the end of 2020.
The Global Vaccine Safety Initiative (GVSI) was set up to implement the Blueprint strategy and to provide WHO and partners with a framework for enhancing vaccine pharmacovigilance, that is to better detect, report, and analyse adverse events.
The eight strategic objectives (1-4 pharmacovigilance, 5-8 regulatory system)
- Adverse Event Following Immunisation (AEFI) detection
- Investigation of safety signals
- Vaccine safety communication
- Tools and methods
- Regulatory framework
- Technical support and trainings
- Global Analysis and response
- Public-private information exchange
How it works: A Global Vaccine Safety Initiative (GVSI) meeting is a general meeting which guides the GVSI, who is the implementation mechanism for the Global Vaccine Safety Blueprint. [2, 3]
As of 2021 the GVS Blueprint is under review, which began December 2018 and again June 2019, in line with deploying the new plan, Immunization Agenda 2030 at the 73rd World Health Assembly in May 2020. No longer will vaccines be focused be on the ” the world’s poorest countries” they intend to “leave no one behind”.
In the 2019 report a “emerging vaccine safety themes” concluded one was “vaccine hesitancy and misinformation” [pg26]
Paper cautions use of coronavirus vaccine in humans
A paper published on April 20, 2012 which tested 4 candidate SARS coronavirus vaccines in both ferrets, monkeys and mice, warned: “Caution in proceeding to application of a SARS-CoV vaccine in humans is indicated”. Many mice that received a virus-like-particle vaccine died when challenged due to immune priming or antibody dependent enhancement (ADE). Although the vaccine induced immune response (producing “serum neutralizing antibodies” said to “protection against infection”), it actually set the mice up for an enhanced reaction upon challenge causing an “immunopathologic-type lung disease”, and death. [1]
Immune inhancement following coronavirus vaccines in animals is a well known issue, and in humans dates back to the use of a formalin-inactivated respiratory syncytial virus (RSV) vaccine in infants and toddlers used in 1967. [2]
Dr Fauci testifies to US Government on H5N1 transmissibility research
Dr Anthony Fauci testifies to the Committee on Homeland Security and Governmental Affairs regarding the “important and intense discourse” to recent manuscripts highlighting the potential risks of conducting “dual use research of concern” (DURC) on the H5N1 avian influenza virus.
These dual use experiments, that genetically manipulate pathogens, could “yield new information” and help “identify molecular targets on pathogenic microbes” that can lead to the development of new vaccines, but also has the potential for bioweapon applications, the latter being DURC.
DURC can yield products that if “misapplied…pose a significant threat with broad potential consequences to public health and safety.”
The research is justified because of the worldwide “thread to public health” from seasonal and pandemic influenza, which is said to be “among the leading global cause of death due to infectious diseases” and is estimated by WHO to cause annually between “250,000 to 500,000 influenza-related deaths” globally.
Experimenting to see “which genetic mutations” alter virus transmissibility or pathogenicity using ferrets as models helps with the goal of developing a “universal” influenza vaccine, of which a “prime-boost” gene-based vaccine seems promising.
International drug regulators begin to form the ICMRA
In May 2012 at a high-level seminar hosted by Brazil, just before the 65th World Health Assembly in Geneva, the importance of better coordinating international cooperation among Medical Regulatory Agencies (MRA) was highlighted. This action marked the begining of the coordinated effore to form the International Coalition of Medicines Regulatory Authorities (ICMRA). [1, 2]
In December 2013 the ICMRA was formed when 8 regulatory authorities came together to form the Coalition, with Health Canada as the chair. By 2023 it has attracted 38 global memebers with the World Health Organization as “an observer.”. [3, 4]
In August 2014, in the face of the Ebola outbreak, the 8 ICMRA members (pledged) “committed to enhanced cooperation with the World Health Organization (WHO) and between regulatory agencies” to encourage and fast track “potential new medicines, otherwise known as investigational treatment. This puts ICMRA in their “interim” phase. [5, 6] Then came Zirka in 2016.
On February 10, 2021 the coalition came together to decide what paramaters would be needed to authorise new versions of COVID-19 vaccines. They decided clincal trials would not be required. And so on June 24, 2021, only a few months after the COVID-19 vaccines rolled out around the world, the WHO released new ‘correlates of protection‘ to justify “vaccine efficacy” to authorise updated vaccines. [7, 8] So now every year a new “updated” vaccine can be justified!
UN Rio+20: the Second Earth Summit: “The Future We Want”
On June 20-22, 2012 the first Earth Summit in 20 years was held again in Rio de Janeiro, Brazil this “marks the 40th anniversary of the first major international political conference that specifically had the word “environment” in its title”. Officially knowns as the United Nations Conference on Sustainable Development (Rio+20). The last Earth Summit was held in Rio in 1992. [1, 2, 3] 40th anniversary of the first major international political conference that specifically had the word “environment” in its title
In January 2012 the committee relesed their “Zero Draft” [6] version of what would be the final document titled “The Future We Want” an extension of the Brundtland Commission’s 1987 “Our Common Future” report [6]. Members states were asked to sign onto “10 new sustainable development goals for the planet”. The “zero draft” was developed by the Co-Chairs and Bureau of the UNCSD Preparatory Committee from March 2011 meetings in New York. [5]
The document was allegedly “leaked” to ahead of time [marketing?!]. [4]
Member States adopted the outcome document The Future We Want that launched a process to develop a set of Sustainable Development Goals (SDGs) to build upon the Millennium Development Goals. The SDGs were intended [for] all countries, not just developing countries. This paradigm shift moves away from outdated development assumptions of the past, and ensures no one is left behind.” [7]
“The Conference also adopted ground-breaking guidelines on green economy policies” in the “context of sustainable development and poverty eradication”.
On March 14, 2013, the first 30-member Open Working Group (OWG) met, to develop a proposal on the SDGs, they held a total of 13 meetings between March 2013 and July 2014, formulating a report containing 17 SDGs and 169 targets. The OWG submitted their proposal to the UNGA for consideration and action at its 68th session in September 2014″. [7] Ahead of the pivotoal 2015 GA.
UN World Happiness Day is born – brining together 3 pillars of sustainable development
On April 2, 2012, the United Nations held the first ever High-Level Meeting on Happiness and Wellbeing: Defining a New Economic Paradigm. At this meeting “United Nations Secretary-General Ban Ki-Moon said, “We need a new economic paradigm that recognizes the parity between the three pillars of sustainable development. Social, economic and environmental well-being are indivisible. Together they define gross global happiness.” [3, 4]
It was attended by Australia’s Honourable Tim Fisher (comments in report)
UN International Happiness Day was founded by Jayme Illien and “was officially sanctioned by the United Nations in their UN Resolution 66/281 on June 28,2012, because “happiness as a fundamental human right and goal”. It was first celebrated on March 20, 2013 and annually ever since on the same date all over the world.
Why “Happy”, in Oct 2020 World Economic Forum (WEF) tweeted “You will own NOTHING and you WILL BE HAPPY” and The Great Reset. According to the self appointed “leaders” the COVID-19 pandemic presented an “opportunity” for their plan to Build Back Better!
- Who is WEF?
- United Nations World Order
- Agenda 2030 means that land and property ownership will be a thing of the past, as ownership leads to “social injustice” [1, 2]
Annual World Happiness Reports started 2012 interlinking with Sustainable Development – stating independence from UN – NGO Parners.
USDA: First RNA technology vaccine approved – herd-specific vaccines
On September 20, 2012 US based private company Harrisvaccines Inc. announced the US Department of Agriculture (USDA) granted the first licence for a RNA technology vaccine to be used in livestock, this for swine influenza virus (SIV) H3N2. The USDA also approved Harrisvaccines manufacturing facility to make any future animal vaccine. [1]
With this new RNA technology platform “only a gene from an infected animal is required to prepare vaccines in as little as four weeks” allowing the company to “rapidly respond to pandemics” in livestock. In 2013 Harrisvaccines gained exclusive rights to Alphavax’s technology for use with companion animals.
The advanced process, called SirraVax RNA Particle (RP) technology, which “utilizes a genetic sequence of specific viruses, which can be submitted electronically, to create a vaccine.” This unique technology allows for the production of custom, herd-specific vaccines in a matter of weeks to “rapidly mutating viruses”…”allowing for rapid response to disease outbreaks” both viral or bacterial.
When the H1N1 virus presented itself we were able to develop a custom vaccine in weeks and were the first to get it to market. That proved that we were prepared to change the landscape in regards to livestock immunology.”
says Joel Harris, Head of Sales and Marketing
Harrisvaccines was founded in 2006 in conjuntion with Uni Iowa, in 2015 they were purchased by Merck Animal Health. In 2016 the USDA grants full license of the vaccine technology platform.
Edible Vaccines – MORE
MERS: first case reported in Saudi Arabia
On September 20, 2012, a report appeared on ProMed from Saudi Arabia of a case of a novel coronavirus isolated from a male aged 60 years, who died 3 months earlier on June 6, 2012. [1, 2]
The novel betacoronavirus (HCoV-EM) was in time classified as Middle Eastern respiratory syndrome coronavirus (MERS-CoV), the virus does not seem to pass easily from person to person. [6]
Early genetic characterization led to the recognition that MERS-CoV was related to SARS-CoV and was thought to have a bat reservoir, and transferred through a camel.
As of October 2021 there have been 2578 MERS cases over 27 countries with 888 deaths reported since April 2012, making a global case fatality rate of 34.4%. [4, 5, 7]
“The emergence of new infectious global threats in the past four decades (e.g. AIDS, H5N1, SARS) has reshaped thinking at the national and international level on the nature and level of public health responses needed for these threats.” [3]
Scientists warning about Tween 80, a common vaccine ingredient
A paper by Qiu et al, from November 2012 raised “concerns with regard to the indiscriminate use of Tween® 80 in clinical applications” as it is an “extensively used surfactant in parenteral drug formulation”. Tween 80 is otherwise known as PolySorbate 80 and is a common surfactant ingredient used in vaccines.
The paper stated that “Tween® 80 induced the release of histamine, and a 2-fold increase in SC5b-9, 2.5-fold increase in C4d, 1.3-fold increase in Bb, while IgE remained unchanged. It also produced changes in pulmonary pressure, systemic pressure and ECG.”
This may explain the anaphylaxis adverse events seen following the COVID-19 jabs. [1, 2]
Australia: DOD+Dept. Health join Medical Countermeasures Consortium (MCMC)
In 2006 Australia became a signatory to the chemical, biological and radiological (CBR) threats, Memorandum of Understanding (MoU) in partnership with the Defence departments of the United States, United Kingdom and Canada. The Medical Countermeasures Consortium (MCMC) is a working group under the CBR MoU and includes the Health Departments of each of those nations. [2]
Medical countermeasures (MCM) include therapeutics (drugs), vaccines, diagnostics and personal protective equipment. Not having MCM “to chemical, biological and radiological (CBR) threats, emerging infectious diseases or pandemics is the biggest risk to our health, economy and security”. [1]
In November 2012, Australia’s Departments of Health joined the Department of Defence (DOD), which in Australia is represented by the Defence Science and Technology Organisation (DSTO) and the Office of Health Protection (OHP), who have been working with local biotechnology and medical-technology communities to identify, validate and develop national MCM-related capability and capacity. [1, 2, 3]
A 2013 DSTO commissioned the first MCM audit which recommended the establishment of a public–private partnership to create a nexus between industry best-practice project/product development disciplines with relevant capabilities in government, universities, medical research institutes and the private sector, resulting in the September 2013 formation of Medical Countermeasure Products Australia (MCPA) with Leigh Farrell is chairman of Steering Committee and Craig Rayner [6] is chairman of Development Committee. Under Next Generation Technology Fund (NGTF), part of Defense Science and Technology (DTS) group. [2, 3, 4, 5]
- In December 2022, Dr Craig Rayner joined Moderna in Australia! He was against ivermectin in 2020!, and in 2017 authored the report to DOD warning that Australia is not prepared, as we import 90% of our drugs! [2]
In 2014 the DOD and Health is represented by the Defence Science and Technology Organisation (DSTO) and the Office of Health Protection (OHP), have been working with local biotechnology and medical-technology communities to identify, validate and develop national MCM-related capability and capacity. [2]
On August 9, 2023 Australian Senator Malcolm Roberts pointed out that this DOD agreement appears to have been designed to make pandemic response in Australia a military operation and not a civilian health operation, especially, when in July 2021, General Frewen took to the microphone in full military uniform. [6]
“The military should not be used against law-abiding civilians or against healthy civilians for the purposes of forced injections to transfer wealth to big pharma”
Senator Roberts stated
The military played a dominant role in the response to the SARS-CoV-2 virus both in the development and distribution of the COVID-19 vaccines, “a fact hidden from the general public”. The TGA allowed the genetic therapy injectable products to enter the Provisional Registration pathway under the classification of a “vaccine”, but it appears they were also considered to be emergency “countermeasures“. So not only were the products not considered a gene therapy, as a “countermeasure” the products circumvented the “standard steps and procedures, otherwise required for pharmaceutical products.” [7]
- On March 2, 2020 President Donald Trump held a meeting to discuss the development of “countermeasures in the form of therapeutics and vaccines.”
TGA: Advisory Committee on the Safety of Vaccines (ACOSV) is established, the precursor to ACV
On November 12, 2012 Australia‘s drug regulator the TGA began recruiting members for the newly established Advisory Committee on the Safety of Vaccines (ACOSV) as regulated “under Part 6 Division 1EB of the Therapeutic Goods Regulations 1990 (the regulations)” the purpose of this body is to “advise and make recommendations to the Minister for Health and the Therapeutic Goods Administration (TGA) on the safety, risk assessment and risk management of vaccines.”
- The committees inaugural meeting was held on March 13, 2013
- TGA has international harmonisation arms
- In Feb 2012 the WHO set a Blueprint for WHO Global Vaccine Safety Initiative
ACSOV handled vaccine safety and risk assessment only and all other “pre-market functions for vaccines” was handled by the Advisory Committee on Prescription Medicines (ACPM).
On January 1, 2017 as part of Government’s October 2016 [5] statutory structural changes, ACSOV and ACPM’s vaccine regulatory roles were consolidated [1] to form TGA’s Advisory Committee on Vaccines (ACV). ACV now “provides independent medical and scientific advice…on issues relating to the safety, quality and efficacy of vaccines supplied in Australia including issues relating to pre-market assessment, post-market monitoring and safe use in national immunisation programs.” [2, 3, 4]
ACV’s role as a statutory advisory committee established by the Therapeutic Goods Regulations 1990, is to hold regular meetings to assess commercial-in-confidence sponsor information in regard to Submissions for Registration, Pharmacovigilance and Immunisation Programs, and provide independent expert scientific and technical advice aid the TGA delegate in making regulatory decisions. ALL advisory decisions now made by one centralised committee!
The ACV was first chaired by Prof. Allen Cheng, with 9 other members. Cheng held additional gate-keeper-like “independent”, highly influential head positions on ATAGI and AusVaxSafety through 2020.
100,000 Genome Project launched – towards genomic medicine
On December 10, 2012, then Prime Minister of UK, David Cameron, launched the 100,000 Genome Project, England’s first mission to sequence 100,000 human genomes by the end of 2017. The initiative is ” paving the way for a digital NHS, where genomics is “driving the move away from a ‘one size fits all’ approach to treatment, towards personalised, or precision medicine, whereby each patient is treated according to their individual genome sequence.” [1, 2]
Prior genome sequencing ventures launched:
Germany runs a Novel Coronavirus simulation
Germany ran a novel coronavirus simulation on an event said to occur once in a 100 years.
This simulated event was based on the scenario of a hypothetical novel coronavirus called “Modi-SARS”, that originated in a SE Asia wild animal market, that “naturally” jumps from animal to human. It takes some weeks for the Chinese to discover the virus, and as such it will spread through out the world.
The incubation period ranged from 2 to 14 days, children are at lesser risk compared to over 65 years. A person is only infectious when they show clear symptoms of the disease. No drugs are available, and a vaccine is 3 years away, and lockdowns are needed until then. Mutations of the virus means there is no immunity!
6 million are expected to become ill in the first wave!
Translate German to English here.
Dr Fauci defines Gain-of-Function research
While presenting at an International Consultative Workshop on “Gain-of-Function Research on Highly Pathogenic Avian Influenza H5N1 Viruses”, Dr Anthony Fauci defines Gain of Function (GOF) research by specifically stating:
“[w]hat historically investigators have done is to actually create gain-of-function by making mutations, passage adoption, or other genetic techniques, such as reverse genetics.”
These “reverse genetics” techniques were used in the Wuhan lab for coronavirus research, using grant funds from the NIH.
This 2012 definition of GOF is contrary to Dr Fauci’s congressional testimony in May 11, 2021 [1].
The First World Government Summit
The First Government Summit held February 12-13, 2013, its stated in their report was “not a convention of leading government officials and experts, but …an interactive platform, a knowledge melting pot and an inclusive national assembly, positioning the United Arab Emirate as the destination for government innovation, regionally.” With a focus on government services, including health. Australia participated.
By 2016 it is known as the World Government Summit (WGS) an annual gathering and “is the primary global forum dedicated to shaping the future of government worldwide”. It is a “neutral, non-profit organization” that “is a knowledge exchange platform at the intersection between government, futurism, technology and innovation. It functions as a thought leadership platform and networking hub for policymakers, experts and pioneers in human development.” [1] Its intended to “inspire and enable the next generation of governments.”
- It has a range of global partners, and requires membership.
- With past speakers like Klaus Schwab [2, 4] , Elon Musk [3], IMF & World Bank and Oxford University.
- In 2014 they partnered with WEF to publish the “Future of Government“
- 2018 – ask institutes to realign with the “global transition to the “new world order” [5]
- They have a vision for 2071
- “COVID-19 and Government“
- Guiding changes to the global Health Care system and more covering all the “sustainable” topics.
2022 – Programmable digital money announced at 2022 WGS
China’s Xi Jinping announces Belt & Road initiative
In Kazakhstan on September 7, 2013 China’s President, Xi Jinping, announced an initiative to build an “economic belt along the Silk Road”, where China would invest in infrastructure and energy in nearly 70 countries and international organizations. This was later referred to as the Belt & Road Initiative (BRI). [1, 2]
In 2017, the BRI was incorporated into the CCP’s constitution, resulting in an additional 61 countries joining in 2018 alone, and by 2021 a total of 139 countries are formally affiliated with China’s initiative, though not Australia. [3]
The project has a target completion date of 2049, which would coincide with the centennial of the People’s Republic of China (PRC)’s founding.
Private firm, CEFC China Energy Company Limited was part of the BRI build. CEFC Chairman, Ye Jianming, and China’s “Spy Chief”, Patrick Ho had business dealings with Hunter Biden, son of the then Vice President Biden (“the big guy“). [4]
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