2022 marks the beginning of the third year of the COVID-19 pandemic.

The Highwire recaps the past 100 Episodes covering COVID-19 pandemic. – WATCH

In a Nature article published January 5, 2022, it points to mounting evidence from animal studies that Omicron is poor at infecting deep lung tissue, making it “less dangerous”, the exact prediction made by Dr Malone on December 15, 2021.

Based on modeling, the Omicron variant may have an 88% likelihood of escaping current vaccines, and studies are revealing breakthrough cases with Omicron.  In lay terms, the spike protein mutations are too great for the vaccine-induced Wuhan spike antibodies to neutralise.  The same appears true for previous natural infection, though second infection is mild.

Despite closed borders and very high vaccination rates, the highly transmissible omicron variant has been reported in seven out of 31 provinces and all of China’s biggest cities after it was first detected December 9, 2021

China’s first community outbreak of Omicron was detected in the city of Tianjin on Jan 8, 2022 in 2 patients, prompting ab immediate government lockdown of the local districts followed by large-scale screening.   41 positive cases were reported as of Jan 11, the source of the transmission is unknown, and the virus is still spreading.

China, which is set to host the Winter Olympics in Beijing starting February 4th, has adopted a “zero-covid” policy, which if an infection is detected it triggers strict control measures such as city lockdowns, factory shutdowns and delivery standstills, including the shut down of ports.  These strict measure have an onflow effect to the global supply chain. [1, 2]

Just before release of Fauci’s damning emails, a letter was sent from US Senate committee to HHS seeking to find truth about the origins of the pandemic virus.  It is stated that “rather than be transparent with the Committee, HHS and NIH continue to hide, obfuscate, and shield the truth” by hiding information that will help inform the origins of the virus.

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An insurance company refused to pay out on a multi-million dollar life insurance policy, after it was confirmed the man died from a COVID-19 vaccination. A French court ruled in favour of the life insurance company because it is know the vaccine is “experimental” and as such is a risky undertaking, essentially “suicide”, which is excluded from the insurance contract. [1, 2]

March 16, 2022, according to AFLD,  America’s Life Insurance council now says that Life Insurance policies may deny payment if you die from the COVID-19 vaccine because they are experimental.

On January 17, 2022, Oxfam’s “Inequity Kills” report was released and states “The wealth of the 10 richest men has doubled, while the incomes of 99% of humanity are worse off, because of COVID-19″.

The wealth of the 10 riches men amounts to $1.9 trillion, grew at a rate of $1.6 billion a day, more than it did the previous 14 years.

“This is the biggest annual increase in billionaire wealth since records began.”

“We have a situation where 10 men hold more wealth than that of two-thirds of humanity”
said Lyn Morgain, chief executive of Oxfam Australia.

Oxfam’s 2021 report revealed the COVID-19 vaccines had created 9 new billionaires.

Over the past two years, the wealth of Australia’s 47 billionaires has doubled to $255 billion. [1]

In a January 19, 2022 Public Health Scotland “COVID-19 & Winter Statistical Report“, figure 13 revealed the unvaccinated having the lowest COVID-19 case rate per 100,000 of all population cohorts, but they warn it should not be an indicator of the vaccines failing to “work.”

“a simple comparison of COVID-19 case rates in those who are vaccinated and unvaccinated should not be used to assess how effective a vaccine is in preventing serious health outcomes, because there are a number of differences between the groups, other than the vaccine itself, and these biases mean that you cannot use the rates to determine how well the vaccines work.”

The World Health Organization’s chief scientist Soumya Swaminathan said during a media briefing on Jan 19, 2022 that there is no evidence that children need booster shots and that the goal needs to “protect those at highest risk of severe disease and dying”. [1]

“There’s no evidence right now that healthy children or healthy adolescents need boosters, no evidence at all.”

In the “Statement on the tenth meeting of the International Health Regulations (2005) Emergency Committee regarding the coronavirus disease (COVID-19) pandemic” on January 19, 2022, amongst other things, the WHO want at least 70% of all countries’ populations vaccinated by the start of July 2022 and they want COVID-19 vaccinations integrated into routine health services. Also “[t]o enhance vaccine uptake, States Parties are encouraged to assess enablers and barriers to vaccination.”

In addition the WHO is calling for the lifting of international travel restrictions and they Do NOT require proof of vaccination against COVID-19 for international travel because currently there’s not enough to go around…not because of health!!!

British Prime Minister Boris Johnson announced “the lifting of COVID-19 vaccine passports, mask mandates and work-from-home guidance in England,” from 20th January, on the back of “wildly incorrect” modelling. [3, 4]

Now with masks the basic policy will be to “trust the judgment of the British people and no longer criminalize anyone who chooses not to wear one.”  The virus is not going to be eradicated, we have to learn to live with it. [1, 2]

The latest COVID-19 variant, the omicron sub-variant, known as BA.2, is 1.5 times more transmissible than the original omicron strain, according to Danish scientists, but just as mild.  UK health say it has a “substantial” growth advantage over the original omicron VOC, known as BA.1.  The mutation difference between BA.1 and BA.2 is greater than the difference between the original “wild strain” and the Alpha variant, where BA.2 has five unique mutations on a key part of the spike protein.

The BA.2 variant was first detected in the Philippines on January 20, 2022, and was soon detected around the world including Australia, around February 3, 2022. [1]

The WHO still considers BA.2 the same Omicron variant of concern.

As requested by the sponsor Gilead Sciences, On January 21, 2022 the FDA granted EUA approval to expand the use of the antiviral drug Veklury (remdesivir) to “certain non-hospitalised adults and pediatric patients for the treatment of mild-to-moderate COVID-19 disease”.   Their justification is that it “provides another treatment option to reduce the risk of hospitalization in high-risk patients”, even with the renal problems. [2]

Previously, the use of remdesivir was limited to patients requiring hospitalization. EUA was first granted in May 2020.

In addition the FDA revised the Emergency Use Authorisation (EUA) for remdesivir to include pediatric infants weighing 3.5 kilograms to children weighing less than 40 kilograms even though there IS NO safety data, and children are not at risk of COVID-19, but certainly at risk of the drug side effects! [1]

US Sen. Ron Johnson (R-Wis.) held a 5 hour panel discussion, COVID 19: A Second Opinion, where a group of world renowned doctors and medical experts provided testimony of a different perspective on the global pandemic response, the current state of knowledge of early and hospital treatment, vaccine efficacy and safety, what went right, what went wrong, what should be done now, and what needs to be addressed long term.

• Attorney Tom Renz – DOD vaccine injury whistleblowers data – WATCH
• Nurse Nicole S first hand experience on the frontline – WATCH
• Dr Marble – telehealth early treatment success – WATCH
• Dr. Peter McCullough Full Highlights – WATCH
• Dr. Paul Alexander Full Highlights- WATCH
• Dr. Paul Marik Full Highlights – WATCH
• Dr. Aaron Kheriarty Full Highlights WATCH
• Dr. Pierre Kory Full Highlights – WATCH
• Dr. Robert Malone Full Highlights – WATCH
• Dr. Ryan Cole Full Highlights – WATCH
• Dr. Richard Urso Full Highlights – WATCH
• Dr. Harvey Risch Full Highlights – WATCH
• Dr. Christina Parks Full Highlights – WATCH
• Steve Kirsch Full Highlights – WATCH

On January 24, 2022, the FDA limits the use of certain Monoclonal Antibodies to treat COVID-19 due to the Omicron Variant, even though we know doctors have been saving lives using Monoclonal Antibodies.. [1, 2]

“Two monoclonal antibody treatments – bamlanivimab and etesevimab (administered together) and REGEN-COV (casirivimab and imdevimab) – to limit their use to only when the patient is likely to have been infected with or exposed to a variant that is susceptible to these treatments” the FDA state “data show these treatments are highly unlikely to be active against the omicron variant, which is circulating at a very high frequency throughout the United States.”

This FDA announcement happened 3 days after the controversial drug remdesivir was granted outpatient approval by the FDA!

A January 24, 2022 paper published in Cell journal, shows vaccine spike antigen and mRNA persist for two months in lymph node germinal centers, which according to Dr Malone is highly unusual.

Dr Malone hypothesises that the substitution of pseudouridine for uridine to avoid the immune response may be working so well that the mRNA is completely evading the normal clearance/degradation pathways. Hence, mRNA that is not being incorporated into cells at the injection site, is migrating to the lymph nodes and continuing to express protein there. In this case, the cytotoxic protein antigen is spike. Spike protein can be detected for at least 60 days after administration of dose. Note that the duration of the protein expression was only tested for 60 days.

The mRNA in the vaccines may not be as self-destructing as they predicted

Protein production of spike in people vaccinated with the Moderna or Pfizer mRNA vaccines is higher than in patients who are severely ill with COVID-19!

On January 27, 2022 parents are told that it is safe for their child to receive the COVID-19 vaccine with other childhood vaccines 9concomitantly), yet no such safety data on the simultaneous administration of COVID-19 vaccines and other vaccines are available for them to read. [1]

ACIP has a history of “no information available” regarding co-administering childhood vaccines, yet they say just stick it in different limbs, as though the body is compartmentalised! [@2:30 ]

The protection people experience after recovering from COVID-19, known widely as natural immunity, lasts for at least 18 months, according to a recently published study, “This is the longest observation (March 2020-September 2021) for the presence of antibodies against SARS-CoV-2 in recovered individuals”.   Those who also received the vaccine showed it gave a “boost” but it waned quickly.  [1]

In a press release on January 31, 2022, the FDA announced the approval of the vaccine which under EUA has been known as Moderna COVID-19 Vaccine, but now approved the vaccine will be marketed as Spikevax for the prevention of COVID-19 in individuals 18 years of age and older, under BLA.  This is the second approved COVID-19 vaccine.  Pfizer’s Cominarty was granted registration August 2021 yet it is still not available in the USA.

Good Sciencing website has been tracking athletes from over the world who have collapsed and or died on the field since the COVID-19 vaccine rollouts began.  As of Feb 5, 2022 they have gathered 624 reports, of which 397 died, and it increases nearly every day.

By June 4, 2022,  1090 Athlete have suffered a cardiac arrest or other serious issues and 715 Died.

Pfizer says it raked in $36.8 billion in COVID-19 vaccine sales in 2021, making it among the best-selling drugs in history, and representing 45% of their product sales, which is projected to reach $100 billion in Q4 2022 [1]

Pfizer is expected to take their new mRNA technology, that has been “accepted” by the global population through the emergency use authorisation, and expand it into other diseases in collaboration with CODEX DNA. Acuitas Lipid Nanoparticles is also “an essential part of everything you do with mRNA” says Pfizer [2]

On February 10, 2022 the Australian Technical Advisory Group on Immunisation (ATAGI) updated the defining of COVID-19 vaccination status from “fully vaccinated” which served for the 2-dose practice, but with boosters now in place they introduce the terminology of being “up-to-date”.  ” It forms the basis of the due and overdue rules for the Australian Immunisation Register (AIR).” [1, 2]

With any of the TGA provisionally approved CV19 vaccines (except J&J), 14 days post the second jab, is a minimum valid time frame for the primary doses to be considered ‘up-to-date’.”  Booster eligibility is from 3 months after the last primary dose, which includes that 14 day wait time – so actually 2 1/2 months.  “People who have not received a booster within 6 months of completing their primary series will be considered overdue”.

The FDA’s plan to fast-track Pfizer‘s COVID-19 vaccine for children under 5 years old (24 million kids) was delayed because

“there’s a low number of cases overall in the clinical trial most kids are not getting symptomatic COVID as such one case in one direction or another can tip the perception of the vaccines overall defectiveness”
says Pfizer director (former FDA commissioner) Dr. Scott Gottlieb

On February 17, 2022, the Therapeutic Goods Administration (TGA) granted provisional registration for the Moderna COVID-19 vaccine, SPIKEVAX, for children aged 6-11 years, to be administered as a half dose of 0.25 mL or 50 micrograms (50μg), in 2 doses at least 28 days apart. Compared to 12 years and older who receive the same vaccine preparation but at full dose of 0.5 mL or 100 micrograms (100 μg). [1, 2, 10]

The TGA state their assessment was based on Moderna‘s  kidCOVE study [3, 4, 5, 6, 7, 8]

By this stage myocarditis is known as a potential side effect of the mRNA COVID-19 vaccines, and have been designated “very rare” which means “up to one in 10,000 vaccinated people may be affected” and “the data show that the increased risk of myocarditis after vaccination is highest in younger males.” [9]

As of Feb. 23, 2022,  49.4% of children have received their first dose of a vaccine and 62.1% of eligible of Australians have received their boosters.

On February 20, 2022 the New York Times reports that the CDC has collected data on hospitalizations for COVID-19 in the United States and broken it down by age, race and vaccination status, but most of the information has been hidden from the public and independent scientists. [1]

“Two full years into the pandemic, the agency leading the country’s response to the public health emergency [the CDC] has published only a tiny fraction of the data it has collected”, because they claim ” it’s not yet ready for prime time”.  The NY Times goes on to state “[m]uch of the withheld information could help state and local health officials better target their efforts to bring the virus under control.”

Doctors call this hiding of data by a public health agency, “scientific fraud”. [2, 3]

People who contract the Omicron virus variant are unlikely to get re-infected by a subvariant of the virus Danish researchers published in pre-print paper.

Emerging data indicate BA.2, a subvariant of Omicron, is more transmissible—possibly 30 percent more, according to the World Health Organization.

But an analysis of data from national surveillance systems in Denmark, one of approximately 10 countries where BA.2 has become predominant, suggests reinfections are rare. [1]

On February 23, 2022, the WHO selects subsidiary of Deutsche Telekom called T-Systems as the contractor to “standardize the issuing of QR codes” for 194 member states for an intended global vaccine passport. [1, 2, 3, 4, 5]

In August 2021 the WHO released technical specifications and guidance document for Digital Vaccine Passports to countries. [5]

The global digital passport system will be designed for ALL vaccines, not just COVID-19 vaccines, somewhere between 260 and 300 vaccines are in the developmental pipeline, and now with mRNA vaccine technology being “accepted” for COVID-19, that number vaccines “justified” for “disease control” could increase substantially. [6]

President Vladimir Putin of Russia declared the start of a “special military operation” in the Ukraine on February 24 2022 (23rd US time zone) with the goal to:

• “demilitarize” but not occupy the country [4],
• to ensure the security of the people of Donbas region and
• the de-Nazi-fication of the region (the para-military neo-Nazi groups that have allegedly been backed, armed and trained by Western military), [5, 6] and
• to bring human rights violator criminal, neonazis to justice. [1, 2, 3]
• “14,000 people had died in fighting between Ukrainian government forces and eastern Ukrainian separatists before Russia invaded, or as Putin and the Russians see it, before they finally felt forced to respond. Not only to answer those pleas for help, but also to protect their own borders and their own security.” [7]

On February 6, 2024, Tucker Carlson is the first journalist in 2 years to interview Putin, as “you cannot understand this war unless you speak to both sides”.

UK Column WATCH

Russia-Ukraine war timeline – HERE

On February 25, 2022 a peer reviewed paper of an in vitro study out of Sweden shows that the Pfizer-BioNTech COVID-19 mRNA vaccine (BNT162b2) spike genetic mRNA code does indeed integrate (reverse transcribe) into liver cell DNA in as fast as 6 hours.   [1, 2, 3]

From early 2021 the media “fact checkers” were debunking this as a possible mechanism or concern, including Australia’s Dept. of Health, and experts. More studies are urgently needed. [4, 5, 6]

This potential “phenomenon” that was NOT looked at and ruled out by the vaccine manufactures and the regulatory authorities before the vaccines were authorised.  The implications and potential consequences of a foreign piece of genetic code incorporating into cell DNA is scary – especially for children! [7]

Watch >>>

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..

On April 18-22, 2022 the annual World Vaccine Congress in Washington DC was held with “record attendance with just under 1900 participants”, a place where academia, pharma and public health intersect!

The World Vaccine Congress is the largest, most established meeting dedicated to vaccines that covers the whole vaccine value chain. [3]

Hatice Beton, Executive Director of the G20 & G7 Health and Development Partnership who leads the policy, advocacy and communications work of over 25 leading global health organisations, discussed solutions to “tackle lowering immunization rates and vaccine hesitancy globally”, which has been labelled a threat to the next pandemic with Disease X. [1, 2]

To be allowed entry to the first face-to-face congress in 2 years all delegates were required to provide “evidence of either full vaccination or a negative PCR or antigen test from within the past 72 hours” for COVID-19,  meaning you could be “vaccine hesitant” and still attend the pro-vaccine conference.

Bill Gates, who is rich (and gets richer through investing in vaccines), believes, as is summarised by Today host (@2min) that “disease is inevitable but pandemics are not, and if you spend billions now you save trillions later”, if only they could get eliminate “vaccine hesitancy”. [4]

The Canadian media picks up on the conclusions of a scientific paper published in a Canadian journal on April 25, 2022, that allegedly concludes from computer modelling that unvaccinated people increase COVID-19 risk of transmission, compared to the vaccinated.

BUT…

Dr Byram Bridle in his substack article walks through how a simple change to just one “assumption” entered in to the mathematical model “completely reverses the conclusions of the paper”. “Now the ‘unvaccinated’ are serving as a protective buffer for the ‘vaccinated.’”

How could such a paper get through peer review and be published?

Mathematical models (that generally have not been made public) have been used in South Australia [1, 2] and globally by Public Health to shape COVID-19 policy, their outputs are only as accurate as the inputs!  One change to the computer model parameters took the unvaccinated from “dangerous” to “heros”!

Peer reviewed, observational study looking at “Increased emergency cardiovascular events among under-40 population in Israel during vaccine rollout and third COVID-19 wave” was published April 28, 2022 in Nature.  Is there a primary cardiac cause? – WATCH

On 7 May 2022, WHO was informed of a confirmed case of monkeypox in an individual who returned from Nigeria where the disease is endemic.   The case developed a rash on 29 April 2022 and arrived in the United Kingdom on 4 May, departing Nigeria on 3 May.

By May 22 the WHO reported on Twitter that there are 11 non-enemic countries with “about 80 confirmed cases, and 50 pending investigations” with more likely to be reported, and travel links have not been established. Endemic monkeypox disease is normally geographically limited to West and Central Africa. [1, 2]

It is reported that monkeypox has been found in an ‘atypical’ spread in several countries including the United States, Spain, Canada and Australia, and “could accelerate in the coming months”, prompting an emergency meeting by the WHO.

This world’s first-ever global outbreak of Monkeypox has occurred, just one year after an international biosecurity conference in Munich held a simulation of a “global pandemic involving an unusual strain of Monkeypox” beginning in mid-May 2022! [3]

The UK is stockpiling vaccines as they fear cases are being missed, as the majority of cases are not linked, suggesting it is spreading more widely.

Bill Gates “warned” us of smallpox in November 4, 2021.  Is it a coincidence the smallpox vaccine also does monkeypox and just in time?  On Sept 24, 2019, 13 months after it’s submission, the FDA approved the smallpox/monkeypox vaccine called JYNNEOS in a country where the virus is not endemic.

The general, healthy population doesn’t need to worry about monkeypox, the public health response need to be focused on male to male sex group – Dr McCullough concurs.  The media are using images of shingles and smallpox to pass off as monkeypox, and COVID-19 vaccine side effects can result in Bullous pemphigoid, painful skin blisters, that could be misdiagnosed as monkeypox.

On May 8, 2022, the FDA officials now admit Americans should treat COVID-19 like the flu, a “departure from the rhetoric that was expressed by public health officials in 2020 and 2021.”

“…it is time to accept that the presence of SARS-CoV-2, the virus that causes COVID-19, is the new normal.”

Frontline doctors have been stating COVID-19 is like the flu since the early data came out in 2020 showing the survival rate for infection is 99.9% for the majority of the population, and they were called out for spreading “disinformation”.