On February 25, 2022, New Zealand High Court judge, Justice Francis Cooke, determined that “the government [vaccine] mandate is an unjustified incursion on the Bill of Rights.” The judge ends Jacinda Ardern’s Vaccine Mandate: “It’s a Gross Violation of Human Rights”.  The landmark case means that the police and Defence staff cannot be fired for refusing to take the experimental COVID-19 vaccines. This case will be used to overthrow all of Ardern’s illegal mandates in New Zealand.

On 3 March 2022, the EU Council adopted a decision to authorise the opening of negotiations for an international agreement on pandemic prevention, preparedness and response or “pandemic treaty“. [1]  In November 2021  the WHO noted this is because the “global response to COVID-19 was a disorganized, inequitable disaster”.

The intergovernmental negotiating body (INB) formed in December 2021, tasked with drafting and negotiating this “international instrument”, will deliver a progress report to the WHO’s 76th World Health Assembly in 2023, with the aim to adopt the international legally binding instrument by 2024, providing the WHO unprecedented powers. [2, 3]

This is the continuation of an “effort to make the WHO the centre of a One World Government” with their One Health agenda – WATCH

But the United States believe a new “Pandemic Treaty” is too slow, so in January 18, 2022 they have proposed changes to the existing IHR which the WHO D-G sent to Member states on January 20, 2022, they want these amendments rushed through at the May 22, 2022 World Health Assembly. [4]

Dr Tess Lawrie in conjunction with Oracle Films released a mini-documentary that captures her attempts to get ivermectin recognised as a drug that would save lives from COVID-19.  The pooled data showed an 90% mortality benefit, and the health “establishment” quashed it. [1]

Yet the global drug regulators and health authorities warned against the established, Nobel Prize winning drug ivermectin for use for COVID-19!  The media got hold of this and falsely portrayed it as only a horse dewormer, not crediting it as a life-saving human medication. [2, 3, 4]

Pfizer CEO, Albert Bourla, admits that the company had only worked with mRNA vaccines for 2 years prior to 2020, before they began their mass experiment on the world population.  The governments, health authorities and the mainstream media told the public that there were decades of experience with mRNA vaccines. [@10min]

“It was counter-intuitive because Pfizer was mastering or let’s say we had very good experience and expertise with multiple technologies that could give a vaccine…mRNA was the technology that we had less experience with, only two years working on this. And actually, mRNA was a technology that never delivered a single product until that day. Not vaccine, not any other medicine, so it was very counter-intuitive and I was surprised when they suggested to me that this is the way to go…

They felt that the two years of work, on mRNA since 2018, together with BioNTech to develop a flu vaccine made them believe that the technology is mature and we are at the cusp of delivering a product, so they convinced me”  says Albert Bourla

On March 4, 2020 the US CDC changed how death certificates were to be filled in for COVID-19, a manner that would exaggerate death numbers.

Two years later on March 10, 2022 the US Health Department in Massachusetts acknowledge they counted the death of any person who had previously tested positive for COVID-19 as a COVID-related death, regardless of how much time elapsed between those two events.  They have now changed the definition so the death number is 15% lower.

Australians looked to the high COVID-19 death toll in countries like the US as an example of what could happen here!

On March 21, 2022, Dr Anthony Fauci et al published a paper to further propagate the notion  that “classical herd immunity” may not be “attainable” for COVID-19.  “The authors explain how the scientific understanding of herd immunity and its applications to various diseases have evolved over time.” [1]

Some factors that Dr Fauci et al believe hinder achieving herd immunity for SARS-CoV-2 include: “the virus’ ability to continually mutate to new variants; asymptomatic virus transmission, which complicates public health control strategies; the inability of prior infection or vaccination to provide durable protection against reinfection; suboptimal vaccination coverage; and adherence to non-pharmacologic interventions.”

“Research to develop pan-coronavirus vaccines, which could protect against multiple coronaviruses or at least multiple SARS-CoV-2 variants, remains crucial.”  Remember in March 2020 getting a vaccine was the only way, this is the next step!  [2]

Ten days later, on March 31st, the NIH launched their clinical trials for mRNA multi-variant vaccines; a solution they’ll likely come to promote!

Without TGA’s approval, on March 25, 2022, ATAGI recommended a fourth dose (second booster), in some cases a 5th dose, of COVID-19 vaccine be given for certain groups and no shorter than 3 months apart.

“Comirnaty (Pfizer) or Spikevax (Moderna) are the preferred vaccines for COVID-19 booster doses including the additional winter booster dose. Vaxzevria (AstraZeneca) can be used when an mRNA vaccine is contraindicated or a person declines vaccination with an mRNA vaccine. Nuvaxovid (Novavax) can be used if no other COVID-19 vaccine is considered suitable for that person.”

It would appear that TGA have provided provisional registration for a “booster” dose, and maybe that is expected to cover any number of boosters!

The “winter booster” COVID-19 program is being rolled out with the 2022 influenza vaccination program and ATAGI says both vaccines can be administered at the same time!

ATAGI’s reasoning for the state that “[d]uring the COVID-19 pandemic, there has been reduced circulation of influenza virus and lower levels of influenza vaccine coverage compared with previous years.”  But due to “borders reopening, a resurgence of influenza is expected in 2022.”  Masks and other mitigation efforts are doing nothing, or could it be they’ve returned to testing for ILI again?

Compare Victoria’s Influenza Like Illness (ILI) data for yourself – see Figures 1, 2 and 3 for 2019, 2020, 2021, 2022  for yourself.

Dose upon dose upon dose and mix and match brands and “antigens”….what could go wrong?

March 30, 2022  – Former CDC Director Dr Robert Redfield stated that Bird Flu will jump to humans and be highly fatal in the coming “Great Pandemic” for which COVID-19 was a mere warm-up. [3]

A few days after Dr Redfield’s “prediction” a “new deadly bird flu” began spreading through domestic flocks in America which will contribute to food shortages, though poses low risk to humans. [1, 2]

The U.S. Department of Agriculture is looking into vaccines as an option to protect poultry against deadly bird flu.

On March 31, 2022, the NIH begins clinical trials evaluating the second COVID-19 booster shots in adults with the Moderna mRNA vaccine, the study included new multiple-variant vaccines.  The study is known as the COVID-19 Variant Immunologic Landscape (COVAIL) trial.

Two days earlier on March 29, the CDC recommended the second booster for adults 50 years and older and the immune-compromised.

The NIH will study the Moderna and Pfizer mRNA vaccine, and claim that the “COVID-19 vaccine manufacturers can adjust prototype vaccines to target specific variants, a process similar to how manufacturers update seasonal influenza vaccines every year to target circulating strains…COVAIL trial will gather data on the immune responses induced by prototype vaccines and variant vaccine candidates—including bivalent vaccines, which target two SARS-CoV-2 variants—to inform booster shot recommendations.

Effectively any mRNA code can be readily generated on a computer and synthesised with these new “vaccine platforms“, but the protein-antigen that your body will be tricked into manufacturing could potentially be cytotoxic, as has been shown with the “spike protein”.

“We are looking beyond the Omicron variant to determine the best strategy to protect against future variants,”
said NIAID Director Anthony S. Fauci, M.D.

The challenge is, what will be the new variant?
They’ve thought about that too, the NIH has established the SARS-CoV-2 Assessment of Viral Evolution (SAVE) programme to “address the public health threat caused by the increasing SARS-CoV-2 genomic diversity”, because new “variants jeopardizes the protective antiviral immunity induced after infection or vaccination”.

Two years into the pandemic the Biden administration launch a new website, COVID.gov, “that serves as a portal for information on vaccines, tests, treatments, masks, and the latest on COVID-19.” [1]

At the US FDA’s April 6, 2022 Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting, they discussed “considerations for future COVID-19 vaccine booster doses and the process for selecting specific strains of the SARS-CoV-2 virus for COVID-19 vaccines to address current and emerging variants.” – WATCH

The FDA’s advisory group VRBPAC discussed the “Future Framework” for the first time on April 6, 2022.  “All of the committee members agreed that COVID-19 shots are not working, that boosting multiple times a year was not feasible, and that the shots need to be reformulated. They also unanimously agreed that there are no “correlates of protection” that one can use to predict what antibody levels would be sufficient to prevent SARS-CoV-2 infection.”

The “Future Framework” is a plan to rig the Covid-19 vaccine regulatory process in perpetuity with the so-called “next generation” COVID-19 shots.

The urgency of this matter was pushed because vaccine manufactures wanted a vaccine strain selection by June 2022 in order to deliver shots for autumn supply.

On June 28, 2022, VRBPAC met and voted to move forward with boosters formulated with Wuhan and Omicron variants even though there is little data. [2]

On April 7, 2022 the Therapeutic Goods Administration (TGA) granted Pfizer provisional registration for COVID-19 booster dose for adolescents 12-15 years, which would be a third shot six months after their first two regardless of which previous brand of vaccine used as their primary course. [1]

One day earlier on April 6, 2022, Senator Malcolm Roberts questioned the TGA in a Senate Estimates session, over the safety of boosters for this young age group.

On April 8, 2022 ATAGI met and concluded that based on current data they did not “currently” recommend the booster shot for 12 to 15 year, though they do still “strongly recommended” primary doses for ages 5-15.

Reports of death and serious injury following the jab in all age groups including adolescent keep mounting up.

As of April 19, 2022, over 57 million doses of COVID-19 vaccines had been administered in Australia according to ATAGI who continue to assess appropriateness of boosters for the adolescent age group..