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Last year I was successful in having the Senate inquire into the prospective terms of reference for a Royal Commission into the government response to COVID-19. The Inquiry was held in good faith by Senator Scarr and I thank everyone concerned for their work, which produced a 128 page report full of honesty, decency and common sense. After hearing and reading testimony from multiple highly qualified witnesses, every one of whom called for a Royal Commission.

The Committee recommended a Royal Commission be held and included a comprehensive Terms of Reference that would have uncovered the truth. Last week, the Government provided a response to the Inquiry Report, which stated that the Government does not support a Royal Commission, does not support working with the States to review COVID, does not support the proposed terms of reference and does not support you, the public, having further involvement in the inquiry process.

This is the same Labor Party that took one million dollars from the pharmaceutical industry in 2022/23, including large donations from Pfizer and Astra Zeneca.

Do we have the best government money can buy? You decide.

Transcript

I move: 

That the Senate take note of the document. 

I wish to comment on Legal and Constitutional Affairs References Committee report COVID-19 Royal Commission. Last year, I was successful in having the Senate inquire into the prospective terms of reference for a royal commission into the government response to COVID-19. The inquiry was held, and I thank Senator Paul Scarr for his even-handed treatment of the process and for producing with the secretariat at an excellent report—outstanding! After hearing and reading testimony from multiple highly qualified witnesses, every one of whom called for a royal commission, the committee did, in fact, recommend a royal commission be held. Their report was 128 pages of honesty, decency and common sense. 

Last week, the government provided its response to the report—one-and-a-bit pages. Here’s what it says: ‘The government does not support a royal commission. The government does not support working with the state governments on an inquiry. The government does not support the proposed terms of reference. The government does not support any further public involvement in the inquiry process.’ How can we have an investigation when the government says it does not support working with the state governments, yet it’s got an inquiry underway right now that is not considering the state governments. Instead, the Albanese Labor government will continue with their cover-up inquiry, comprised of two bureaucrats and a university academic closely involved in the COVID response. Shame! The government is letting bureaucrats and academics investigate themselves. What a disgrace! It is betrayal. It’s inhuman.  

During the last election campaign, the Prime Minister promised a royal commission or similar inquiry. A Senate select committee inquiry would fit that description. Then Senator Gallagher promised us a royal commission. No wonder the public distrust politicians, when two promises that were as clear as day were broken the minute the Labor Party came to power. It does raise this question, though: what was the motivation for the government to proceed with a cover-up instead of its promised judicial inquiry? Could it be the donations the Labor Party received from the pharmaceutical industry in the last election?  

Here’s the list from the Australian Electoral Commission of donations made to the Australian Labor Party in 2022-23: AbbVie, the makers of leuprorelin, a puberty blocker, $14,000; Alexion Pharmaceuticals, $33,000; Amgen biopharmaceuticals, $27,500; Aspen Medical, $83,000; AstraZeneca, $33,000, and isn’t there a huge conflict of interest in refusing to investigate them; Bayer, $33,000; Bristol-Myers, $52,000; HA Tech pharmaceuticals, $54,000; and Johnson Johnson pharmaceuticals, $36,000. Kerching, kerching, kerching! The cash register at the Labor Party is ticking over. Here are more donations: Merck Sharpe Dohme, $66,000; Navitas, $33,000; Pfizer, $25,000—another cash register kerchinging. There was Roche, $66,000; Sanofi-Aventis, $42,000; Pharmacy Guild of Australia, who enjoyed years of profit dispensing high-paying COVID injections, $154,000; and Medicines Australia, the peak lobbying body for the pharmaceutical industry, which just gave the former head of the TGA, Professor Skerritt, a job as a director, donated $112,000 to the Labor Party campaign funds—kerching! Including smaller donations, the Labor Party raked in almost a million dollars from pharmaceutical companies and associated favours bought. It’s not just big pharma, either. Remember when you couldn’t get COVID at Bunnings, yet you could get it at your neighbourhood hardware store? Governments forced many hardware stores to stop business during lockdowns, and they went broke while Bunnings grew its market share. Then they set up vaccination stations in their car parks. I know many people thought that was odd, so let’s look at this list of donations. The owners of Bunnings, Wesfarmers, donated $110,000. For completeness, let me list One Nation’s pharma donations in 2022-23: none! There was not one donation from the pharmaceutical industry, the banking industry, the healthcare industry or the net-zero industry. Why? It’s because One Nation is not for sale. 

I will now review what the government is covering up with their refusal to hold a COVID royal commission. This is based on expert witness testimony to the committee inquiry and on peer-reviewed papers and data analysis which have come out since the inquiry. Firstly, testimony before America’s congress proves SARS-CoV-2 was the product of gain-of-function research, with funding from Anthony Fauci’s National Institutes of Health, managed through Peter Daszak’s EcoHealth Alliance. The research started in the USA, and when President Obama banned gain-of-function research, it was moved to the Wuhan Institute of Virology in China. But the research continued secretly and illegally in North Carolina. We know that. In 2021, Australia’s CSIRO confirmed it assisted in the Wuhan research. We’re complicit. 

Secondly, the official timeline for COVID is wrong. The University of Siena in Italy sequenced COVID on 10 October 2019. Unconfirmed reports persist of three lab technicians from Wuhan lab presenting with flu-like symptoms to a hospital in Wuhan in mid-September 2019. Those three were COVID patients ‘zero’. Wuhan has 90 direct overseas flights a day, including five a day into Italy and five a day into Australia, where symptomatic infections started showing up around the end of December 2019. This means that, in October 2019, when the Bill Melinda Gates Foundation sponsored the COVID-themed Event 201 war game that the World Economic Forum organised, COVID was alive in public. Note that the Nobel Prize winning virologist Luc Montagnier sequenced COVID in April 2020 and found: ‘It is not natural. It’s the work of professionals and of molecular biologists—a very meticulous work.’ Luc declared the virus was a combination of the original man-made SARS virus, parts of the HIV virus and a bat virus which was there to fool the body’s immune system into thinking it had never seen the virus before and as a result had no immune response to it. 

The fact the virus escaped before it could be perfected has saved billions of lives. What they tried to do was evil personified. Here is an example. The RNA genome of SARS-CoV-2 consists of 30,000 nucleotides and 11 major coding genes. Pfizer, BioNTech and Moderna took the 4,284 nucleotides constituting the spike protein. At positions K986P and V987P, they introduced mutations to stimulate increased production of human antibodies. Those spike proteins of SARS-CoV-2 are involved in receptor recognition, viral attachment and entry into the host cells. The last part is significant. Both COVID itself and the mutated vaccine material enter human cells. There’s certainty on this point. These COVID vaccines are gene therapies yet are not regulated as such. No safety testing was done on the long-term effect of introducing a mutated COVID DNA strand into the human genome. 

Secondly, Oxford University investigated brain injury from COVID. It mapped the brains of 785 participants and waited for them to get COVID; 401 obliged, creating a control of 384. All were scanned a second time, and any brain function difference was attributed to COVID spike proteins. Oxford University found: ‘significant longitudinal effects, including a reduction in grey matter thickness and tissue contrast, changes in markers of tissue damage in regions functionally connected to the olfactory function and a reduction in global brain size in the SARS-CoV-2 cases. The participants who were infected with SARS-CoV-2 showed on average a greater cognitive decline between the two time points.’ The paper concluded these results may indicate degenerative spread of the disease through olfactory pathways through the nose. Doctors who advocated for nasal preparations were actually right. The nose turns out to be the key. One study found 471 bacterial agents in 171 face masks, many of which had high resistance to antibiotics. This was an important issue for the royal commission to understand. Thirdly, Yonker et al. from Massachusetts General Hospital tested young people presenting with chest pains and found free spike antigen was detected in the blood of adolescents and young adults who developed post-mRNA-vaccine myocarditis, linking the shots with heart disease in the young. Fourthly, we knew as early as November 2021 that spike protein could build up in the lungs, heart, kidney and liver, causing an inflammatory response, yet we kept injecting spike proteins into people, including children, over and over. Now they’re dying suddenly and doctors are baffled—the hell they’re baffled. 

Fifthly, SARS-CoV-2 spike proteins, meaning most likely the shots as well, have serious effects on the vasculature of multiple organ systems, including the brain. Outcomes include fatal microclot formation and, in rare cases, encephalitis. Wait a minute. Isn’t New South Wales now urging parents to vaccinate their children against a sudden outbreak of encephalitis? COVID and COVID shots are the same man-made poison, yet we never tested the shots long enough to reveal that. Now people are dying and suffering life-altering disease while we continue to inject the public with boosters containing the very substance that is causing these deaths and injuries. 

Today I’m announcing that, in the first week of December, I will be conducting the third of my full-day reviews of COVID, to be called ‘COVID in trial’. I promise to hound those responsible— 

The ACTING DEPUTY PRESIDENT (Senator Allman-Payne): Thank you, Senator Roberts. Do you wish to seek leave to continue your remarks? 

Senator ROBERTS: Yes, I seek leave to continue my remarks. 

Leave granted. 

References

https://oversight.house.gov/release/hearing‐wrap‐up‐dr‐fauci‐held‐publicly‐accountable‐by‐select‐subcommittee/

https://www.csiro.au/en/news/all/news/2021/june/response‐to‐the‐australian‐25‐june‐2021

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778320/

https://www.weforum.org/press/2019/10/live‐simulation‐exercise‐to‐prepare‐public‐and‐private‐leaders‐for‐pandemic‐response/

http://www.xinhuanet.com/english/2020‐04/21/c_138995413.htm

https://onlinelibrary.wiley.com/doi/10.1002/prca.202300048

https://www.nature.com/articles/s41586‐022‐04569‐5

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883076/

https://pubmed.ncbi.nlm.nih.gov/36597886/

https://www.nature.com/articles/s42003‐021‐02856‐x

https://pubmed.ncbi.nlm.nih.gov/33053430

Recently, I co-sponsored a Bill to establish a Senate Commission of Inquiry into COVID-19 and the government’s response. A Senate Commission of Inquiry is similar to a Royal Commission.

It’s extraordinary that Australia’s most costly and far reaching government response since WWII has not been subjected to an inquiry. This is more than likely because of the serious mistakes made, including poor judgments and instances of cronyism in both the government and the health industry.

I spoke in favour of the Bill, but it was voted down by globalist Liberals and, unsurprisingly, the corporate lackies in the Labor Party. The Greens chose to abstain.

One Nation remains committed to securing a thorough Commission of Inquiry into both the disastrous government response and the origins of COVID-19 itself.

How They Voted

Transcript

One Nation strongly supports the COVID-19 Response Commission of Inquiry Bill 2024, which I’ve proudly co-sponsored. To use the words of a former prime minister, ‘It’s time.’ It’s time to accept our duty is to the Australian people, not to ourselves and our colleagues. It’s time for courage and for truth.  

My Senate office held the first inquiry into COVID and response measures, called COVID Under Question, on 23 March 2022; a second was held on 17 August of the same year. Witnesses included Australian and international experts on health and the relatives of people that the COVID vaccine injections killed or maimed. All aspects of Australia’s COVID response were questioned. Several political parties participated, making it a truly non-partisan, cross-party inquiry. Because of the two full days of testimony at these hearings my decision-making has been better informed ever since. And that’s what senators must do: inform ourselves. 

The increasing interest from mainstream media in reporting the harm our COVID measures have caused indicates time is running out for those engaging in a cover-up. The public remains deeply dissatisfied and gravely concerned about state and federal governments’ COVID response. The people have many questions to be answered before trust can be restored in federal and state governments, politicians, health departments and agencies, medical professionals, medical professions, the media and pharmaceutical companies. 

I find it surprising our health bureaucrats and politicians oppose a judicial inquiry into COVID. After listening to their responses in Senate estimates hearings over the last four years, it’s clear they do not want to admit to a single mistake. In fact, their answers suggest they consider their performance exemplary, worthy of medals and parades. The United Kingdom even called upon the whole country to stand every Thursday evening on their front doorsteps and applaud their health professionals. Can you believe that? The inventor of the Moderna vaccine was given a stage-managed standing ovation at Wimbledon. Certainly, big pharma thought so highly of the head of our TGA, Therapeutic Goods Administration, Professor Skerritt, that they offered him a thankyou job on the board of Medicines Australia, which, despite the grandiose name, is the main pharmaceutical industry lobby group—heady days, indeed. Those days are over. That’s it! To those in this place fighting a rearguard action against the tidal wave of knowledge and accountability, it must now be clear to you that the battle is lost. Public anger is not going away; it’s here to stay until you restore trust. Trust in the medical profession is lower than at any time I can recall, and I fear where that will lead if not corrected. 

Every new unexplained death and every new heartbreak increases public realisation of what was done to our people in Australia. Despite the statistical sleight of hand, excess deaths are not falling. The genetic timebomb of mRNA vaccines is still ticking. More people are dying and more will die. The failure of our regulatory authorities to protect us is a crime. Approving a novel vaccine that killed people is a crime—homicide. Banning existing products that had proven efficacy and safety in order to drive sales of the so-called vaccine is a crime. Finally, covering up this corrupt process is a crime. 

Those who approved the vaccine knew, or rightly should have known, it was a gene therapy of a type which has failed a generation of safety testing. Five United States states—Texas, Utah, Kansas, Mississippi and Louisiana—are currently suing Pfizer for knowingly concealing vaccine caused myocarditis, pericarditis, failed pregnancies and deaths. The complaints allege Pfizer falsely claimed that its vaccine retained high efficacy against variants, despite knowing the reverse to be true—that is, protection dropped quickly over time, and the vaccine did not protect against new variants. Marketing the vaccine as safe and effective, despite its known risks, is a violation of consumer law in these five states. 

The lawsuit alleges that Pfizer engaged in censorship with social media companies to silence people criticising its safety and efficacy claims, proof of which has been public knowledge since Elon Musk released the Twitter files in December 2022. The lawsuit charges civil conspiracy between Pfizer, the US Department of Health and Human Services and others ‘to wilfully conceal, suppress or omit material facts relating to Pfizer’s COVID-19 vaccine.’ Under America’s PREP Act, Pfizer has indemnity for injuries. That indemnity is invalidated through making false and misleading claims. 

The reason this relates to Australia and to Australians is our contract with Pfizer, which provided indemnity against injury, can be negated through Pfizer’s misconduct, and misconduct there was, as I’m sure this commission of inquiry will discover. To taxpayers wondering why the expense of this inquiry is needed, here’s a thought: if we have a chance to move the cost of vaccine harm from the taxpayer to the perpetrator, we must take that opportunity. The guilty should pay; taxpayers should not pay. 

The grand jury evidence gathered to prepare the United States court case from the five states that I mentioned earlier applies to Australia as well. It makes for horrifying reading. First, Pfizer’s chairman and CEO, Dr Bourla, a veterinarian, not a doctor, declined government funding in order to prevent the government’s ability to oversee the vaccine development, testing and manufacture. That’s not something one does with a safe and properly made product. Second, Pfizer’s independence from Operation Warp Speed allowed it to demand a ‘tailor-made contract’ that did not include the normal clauses protecting taxpayers’ interests. Third, the investigation found Pfizer wilfully concealed, suppressed and omitted safety and efficacy data relating to its COVID-19 vaccine and kept them hidden through confidentiality agreements. Fourth, Pfizer had a written agreement with the United States government that Pfizer had to approve any messaging around the vaccine. I suspect the inquiry will find the same arrangement applied in Australia. In effect, Pfizer told our regulators what to say about their product. 

Fifth, Pfizer used an extended study timeline to conceal critical data relating to the safety and effectiveness of its COVID-19 vaccine. The study timeline was repeatedly pushed out to avoid revealing the results of the clinical trials until after billions of doses had been given. I’ll say that again: they avoided revealing the results of the clinical trials until after billions of doses had been given. Sixth, instead, Pfizer submitted a Hollywood version of the safety trials, which showed efficacy and safety that their real trials did not have—and our state and federal health authorities bought it. 

Seventh, we’re three years into COVID and scientists still can’t review Pfizer’s COVID-19 raw trial data. Eighth, so, when Professor Skerritt said in Senate estimates hearings that the TGA, the Therapeutic Goods Administration—his Therapeutic Goods Administration—had analysed all of the trial data, that was a lie. They used Pfizer’s special data. 

Ninth, Pfizer kept its COVID-19 vaccine’s true effects hidden through destroying the trial control group, invalidating the whole study. This was not gold standard research; this was dangerous and fraudulent behaviour. Tenth, Pfizer rigged the trial through excluding individuals who had been diagnosed with COVID-19, who were immunocompromised, pregnant or breastfeeding, or who were simply unwell. Why did the TGA claim the vaccine was safe for these very people when the vaccine was not tested on these people? Eleventh, the statement that the vaccine worked even if you already had COVID is therefore a lie, and yet that lie was used to expand the market and make more money. 

Twelfth, Pfizer maintained its own secret adverse events database, which was obtained in court process, and showed in the first three months of the rollout 158,893 adverse events resulted, including 1,223 deaths. Thirteenth, Pfizer was receiving so many adverse event reports that it had to hire 600 additional, full-time staff. It hired 600 extra people to monitor the adverse event reports. 

And, finally, while Pfizer tested its COVID-19 vaccine on healthy individuals in 2020, Pfizer and its partner, BioNTech, quietly tested its COVID-19 vaccine on pregnant rats. Test rats produced foetuses with severe soft tissue and skeletal malformations, failed to become pregnant and failed to implant embryos at more than double the control group rate. That’s amongst other side effects. Some rats lost their entire litter. Pfizer did not issue a press release announcing the rat fertility study’s findings. And when they were asked, they lied about the outcome. I can’t help but think about women, humans, suffering as a result of this. We know that. 

The United States is achieving what Australia is not—rigorous inquiry and testing of the law. What are you afraid of? In Australia, this is behaviour which, under normal circumstances, would already have resulted in a commission of inquiry. Our delay in calling that inquiry damns us. Other nations are now ahead of us. South Korea has produced a study which analysed 4.3 million individuals—4.3 million!—comparing the rates of various new medical conditions in vaccinated versus unvaccinated groups over three months. The study revealed that the vaccinated experienced a 138 per cent increase in mild cognitive impairment, a 93 per cent increase in sleep disorders, a 23 per cent rise in Alzheimer’s disease, a 44 per cent rise in anxiety and related disorders and a 68 per cent rise in depression. 

In Australia, following my questions to the Australian Institute of Health and Welfare at the inquiry into excess mortality in Australia, evidence was presented that the Australian Institute of Health and Welfare could have done this same research. It chose not to. Our health authorities are not conducting this research because they don’t want to know the answer. They want to hide from the truth, hide from the homicide that’s been caused in this country. I ask the Senate to pass this bill so we can get the answers ourselves, which is, as senators, our sworn duty.  

In March 2022, my office conducted an inquiry titled “COVID Under Question” to examine COVID and the response measures. Another inquiry was held in August of the same year. Witnesses included Australian and international health experts, as well as individuals or loved ones who were impacted by the jabs. The inquiry scrutinised all facets of Australia’s COVID response, involving politicians from multiple parties, ensuring a genuinely non-partisan cross-party inquiry.

Channel 7’s Spotlight program revealed widespread public dissatisfaction and concern with the government’s COVID response. Many people are expressing anger and have numerous unresolved questions. Rebuilding trust in federal and state governments, politicians, health departments, medical professionals, media, and pharmaceutical companies cannot happen without fully addressing these concerns.

Call a COVID Royal Commission now!

Transcript

My Senate office held the first inquiry into COVID and response measures, called COVID Under Question, on Wednesday 23 March 2022. Another was held on Wednesday 17 August of the same year. Witnesses included Australian and international experts on health and relatives of people that the COVID injections killed or maimed. All aspects of Australia’s COVID response were questioned. Politicians from several parties participated, making it a true non-partisan cross-party inquiry. 

Because of the two full days of testimony at these inquiries, my decision-making has been much better informed. That’s what a senator must do. I acknowledge the support of my wife, Christine, as our office team’s workload increased in response to the many serious breaches of Australians’ rights and tens of thousands of deaths due to mandated COVID injections. 

Our aim is to restore our country and our planet for humans to abound and flourish. Channel 7’s Spotlight program two nights ago revealed that the public remains very deeply dissatisfied and concerned about governments’ COVID response. Many are angry. The people have many questions to be answered before trust can be restored in federal and state governments, in politicians, in health departments and agencies, in medical professions, in media and in pharmaceutical companies. 

Across Australia, citizens are waking, making an effort to understand for themselves and for Australia. Generally speaking, people are wonderful and deserve to have their needs and expectations of governments met. Citizens are our constitutional democracy’s highest order. As servants to the people, it’s our duty as their representatives to address their questions and concerns. I find it surprising that our health bureaucrats and politicians oppose a judicial inquiry into COVID. Listening to their responses in Senate estimates over the last four years, it’s clear they desperately do not betray they’ve made a single mistake. In fact, their answers suggest their performance has been exemplary—worthy of medals and parades. The United Kingdom even called upon the whole country to stand on their front doorsteps and applaud their health professionals every Thursday evening. The inventor of the Moderna vaccine was given a staged standing ovation at Wimbledon. Certainly, big pharma thought so highly of the head of the TGA, the Therapeutic Goods Administration, Professor Skerritt, that they offered him a thankyou job on the board of Medicines Australia—which, despite the grandiose name, is the main pharmaceutical industry lobby group. Heady days, indeed. Those days are over as the reality of their incompetence, self-interest and lies comes home to roost. 

To those in this place fighting a rearguard action against a tidal wave of knowledge and accountability, it must be clear to you now that the battle is lost. Public anger is not going away; widespread and deep anger remains. Trust in the medical profession is lower than at any time I can recall. I fear where that will lead if it’s not corrected. 

Every new unexplained death and every new heartbreak increases public realisation of what was done to the people. Excess deaths, despite statistical sleight of hand, are not falling. The genetic timebomb of mRNA vaccines is still ticking. More people are dying and more will die. The failure of our regulatory authorities to protect us is a crime. Approving a vaccine—a novel vaccine that killed people—is a crime. Banning existing products that have proven efficacy and safety in order to drive sales of a so-called vaccine is a crime. Covering up this corrupt process is a crime. This is homicide. Those who approved the vaccine knew, or rightly should have known, it was a gene therapy—an experimental gene therapy of a type which has failed a generation of safety testing. 

Five United States states—Texas, Utah, Kansas, Mississippi and Louisiana—are currently suing Pfizer for knowingly concealing that the vaccine caused myocarditis, pericarditis, failed pregnancies and deaths. The complaints allege Pfizer falsely claimed that its vaccine retained high efficacy against variants despite knowing the reverse was true: protection dropped quickly over time, and it did not protect against new variants. Marketing the vaccine as safe and effective despite its known risks is a violation of consumer law in all five of those states. The lawsuit alleges Pfizer engaged in censorship with social media companies to silence people who were criticising its safety and efficacy claims and who even dared to question them—proof of which has been public knowledge since Elon Musk released the Twitter files in December 2022. 

The lawsuit charges civil conspiracy between Pfizer, the US Department of Health and Human Services and others ‘to wilfully conceal, suppress or omit material facts relating to Pfizer’s COVID-19 vaccine’. While Pfizer has indemnity for injuries, under the PREP Act, that indemnity is invalidated through making false and misleading claims. The reason this relates to Australia as well is that our contract with Pfizer, which provided indemnity against injury, can be negated through misconduct from Pfizer, and misconduct there was. Surely, if we have a chance to move the cost of vaccine harm from the taxpayer to the perpetrator, we must take that opportunity. Citizens of Australia deserve this. 

Evidence for this lawsuit in the United States was gathered during a grand jury investigation and has now been presented to the Supreme Court of the United States, the ultimate court. It makes for horrifying reading. One, Pfizer’s chairman and CEO, Dr Bourla—a veterinarian, not a doctor—declined government funding in order to prevent the government’s ability to oversee the development, testing and manufacture of the vaccine. That’s not something someone does with a safe and properly made product. Two, Pfizer’s independence from Operation Warp Speed allowed it to demand a tailor made contract that did not include the normal clauses protecting taxpayers’ interest. Three, contrary to its representations, Pfizer has wilfully concealed, suppressed and omitted safety and efficacy data relating to its COVID-19 vaccine and has kept data hidden through confidentiality agreements—it kept it hidden. Four, Pfizer had a written agreement with the United States government that Pfizer had to approve any messaging around the vaccine. A judicial inquiry can determine if such a clause was in the Australian agreement as well.  

Five, Pfizer used an extended study timeline to conceal critical data relating to the effectiveness and safety of its COVID-19 vaccine. The study timetable was repeatedly pushed out to avoid revealing the results of the clinical trials until after billions of doses had been given. Six, instead Pfizer submitted a ‘Hollywood’ version of the safety trials, which showed efficacy and safety data that their real trials did not, and our health authorities bought it. 

Seven, we’re three years into COVID, and scientists still can’t review Pfizer’s COVID-19 raw trial data. Eight, so, when Professor Skerritt said in Senate estimates that the TGA had analysed all of the trial data, that was a lie. They used Pfizer’s ‘special’ data. Nine, Pfizer kept the true effects of its COVID-19 vaccine hidden by destroying the trial control group, invalidating the study. This was not gold-standard research. This was dangerous and fraudulent behaviour. 

Ten, Pfizer rigged the trial by excluding individuals who had been diagnosed with COVID-19 or who were immunocompromised, pregnant, breastfeeding or simply unwell. Why did the TGA claim the vaccine was safe for these people when the vaccine was not even tested on these people? Eleven, the statement that the vaccine worked even if you already had COVID is therefore a lie, yet that expanded the potential market. Twelve, Pfizer maintained its own secret adverse-events database, which was obtained in court processes and showed that, in the first three months of the rollout, 159,000 adverse events had resulted, including 1,223 deaths.  

Thirteen, Pfizer was receiving so many adverse-event reports that it had to hire 600 additional full-time staff. Fourteen, while Pfizer tested its COVID-19 vaccine on healthy individuals in 2020, Pfizer and its partner, BioNTech, quietly tested its COVID-19 vaccine on pregnant rats. Subjects had fetuses with severe soft-tissue and skeletal malformations, and some subjects failed, at more than double the rate of the control group, to become pregnant and to implant embryos, amongst other side effects. Some rats lost their entire litter. Pfizer did not issue a press release announcing the rat fertility study findings, and it lied about the outcome. 

My 10 minutes is almost done, and I’m only up to page 24 of the 179-page brief of evidence. There are another 155 pages yet to cover. If it’s not clear to the listeners by now, the vaccine was criminal fraud. I have plenty more to share with you. 

The last word for today is from South Korea, where a study analysed 4.3 million individuals over three months, comparing the rates of various new medical conditions in vaccinated versus unvaccinated groups. The study revealed that the vaccinated experienced a 138 per cent increase in mild cognitive impairment, a 23 per cent rise in Alzheimer’s disease, a 68 per cent rise in depression, a 44 per cent rise in anxiety and related disorders and a 93 per cent increase in sleep disorders.  

In Australia, following my questions to the Institute of Health and Welfare at the inquiry into excess mortality in Australia, evidence was presented that the Institute of Health and Welfare could have done this same research. It chose not to. Our health authorities are not conducting this research because they don’t want to know the answer. They want to avoid the answer and hide the answer. A judicial inquiry is needed to get to the truth, and I call on Prime Minister Albanese to call a royal commission immediately. 

At the last estimates in May, I asked CASA which experts they had consulted for their advice. After some delay, CASA admitted they had relied solely on information from the Chief Medical Officer, without conducting any independent research. They stated their sources were limited to the TGA and FDA and that the only data used came from Pfizer, which has since admitted to numerous fatalities.

Ms. Spence said she was aware AstraZeneca had been withdrawn and that Novavax had also been withdrawn. However, she noted that there had been no reported adverse events in the cockpit.

I raised concerns about CASA’s varying health test requirements for pilots of large commercial aircraft versus small private planes and pointed out that these differing standards posed a risk in shared airspace.

Transcripts

ACTING CHAIR: Thank you to your legal officer. Senator Roberts?  

Senator ROBERTS: Mr Marcelja could not tell me the specific names of the experts upon which CASA relied for turning a blind eye to Qantas and Virgin on mandates, which weren’t government mandates. Dr Manderson, can you tell me specifically which medical experts you relied upon for allowing Qantas and Virgin to mandate the vaccines? Who gave you the advice? Dr Manderson: The chief health officer of Australia at the time would be one important name.  

Senator ROBERTS: Did you actually get his advice?  

Ms Spence: I think we have gone through this previously. I appreciate—  

Senator ROBERTS: That was with Mr Marcelja—  

Ms Spence: But I think what we—  

Senator ROBERTS: and he wouldn’t tell me the names of the chief medical officer—  

Ms Spence: Sorry, Senator. Do you want me to finish?  

Senator ROBERTS: Do you want me to allow you to keep interrupting?  

ACTING CHAIR: Senator Roberts, come on. You know that’s against standing orders.  

Senator ROBERTS: There’s been a lot of protection of—  

ACTING CHAIR: No. Allow Ms Spence to conclude her answer to your first question.  

Senator ROBERTS: She’s not answering my question; Dr Manderson is.  

ACTING CHAIR: I thought I heard Ms Spence, but—  

Senator ROBERTS: She interrupted.  

ACTING CHAIR: I’ll allow CASA to answer your question. CASA?  

Ms Spence: All I was going to say is that we’ve tried to explain before that we don’t get individual advice on specific issues; we rely on the advice of the health experts, and, in this case—as Dr Manderson has said—the chief health officer of Australia was basically a key source. But the TGA was also providing advice. I think we have actually put that in response to questions or in some of the Hansard previously.  

Senator ROBERTS: The reason I’m frying up is that Mr Marcelja said that it was the experts, and he wouldn’t name them, and the experts wouldn’t name them. And then we went to international experts, to I gave up. Your answer is the Chief Medical Officer—not the chief health officer. I presume you’re talking about the federal Chief Medical Officer.  

Ms Spence: Yes.  

Senator ROBERTS: That’s important. The Chief Health Officer is—  

Mr Marcelja: Senator, perhaps you could refer me to your question specifically so that I’ve got in front of me what you’re talking about. What date was that? I’ve got the Hansard in front of me. 

Senator ROBERTS: I can’t remember the date.  

Mr Marcelja: You can’t remember it. My recollection of the conversation was that you were asking me on what basis we were taking the actions we were taking, and I told you that we were taking no actions to intervene in the Australian government’s response. The advice, as Dr Manderson pointed out, about Australia’s response was not being led by us; it was being led by health authorities. So we did not intervene and override the advice of Australia’s Chief Medical Officer or other health experts.  

Senator ROBERTS: You have told me that the buck ends here for aviation safety. You did not do any testing at high-altitude pressures, correct?  

Ms Spence: No.  

Senator ROBERTS: You just assumed Pfizer, the Chief Medical Officer and the TGA knew that the pressure would be okay at high altitude?  

Mr Marcelja: As I tried to explain a moment ago, what we’re interested in from a vaccination or medication perspective is: is it likely that you will get into a cockpit, have a sudden, incapacitating event and be unable to fly the plane? That’s our primary concern. For all vaccinations, including the vaccinations that were being—  

Senator ROBERTS: In the cockpit at altitude.  

Mr Marcelja: at altitude—our primary concern was whether that medication, the vaccination, would cause that event to happen. There is no evidence in Australia or anywhere around the world. We’ve checked with our regulatory authorities and colleagues in the US and Europe. There is no evidence of that event occurring anywhere in the world over the last several years. I think we were on pretty sound footing not to intervene and prevent a particular cohort of the population from being vaccinated when that’s not our role.  

Senator ROBERTS: Let me ask you a few more questions around that. I want you to remember at all times in your answers to me that, when it comes to safety, the buck stops with you, CASA. There is no high-altitude testing done that you’re aware of. Are you aware that the TGA, when I asked them what tests they did in Australia on the vaccines, said they did no tests and relied on the FDA? Are you aware of that?  

Mr Marcelja: I reiterate what I said. They are not matters for us. We look at it from an aviation safety lens. Dr Manderson has been involved in international panels looking at aviation safety on a number of different topics. I’m sure she can step you through that. There is no evidence whatsoever over several years now of there being an aviation safety risk. That’s our concern. Whether the vaccine has other effects or issues—  

Senator ROBERTS: You relied upon the TGA. That was one of the people you relied on.  

Ms Spence: Yes.  

Senator ROBERTS: The TGA admits it did no testing and that it relied upon the FDA. The FDA, prior to the TGA’s announcement, admitted that it did no testing and relied on—wait for it—Pfizer.  

Mr Marcelja: Are you suggesting—  

Senator ROBERTS: Now we find out Pfizer in their trials had hundreds of fatalities.  

Ms Spence: I don’t know how many times we can say this, but we treated the COVID vaccinations the same way we treat all vaccinations, and we don’t do individual, independent testing. But—  

Senator ROBERTS: Let me continue, then. Are you aware of AstraZeneca being withdrawn?  

Ms Spence: Yes, but I think—  

Senator ROBERTS: Are you aware—  

Ms Spence: Senator, sorry. I don’t think it’s quite as clear cut as saying it’s been withdrawn. They’re no longer using it. It wasn’t around inefficacy at the time, but now they’re no longer producing it. Yes, we are aware.  

Senator ROBERTS: Do blood clots say anything to you. What about Novavax? We understand that has been withdrawn just recently.  

Ms Spence: I wasn’t aware of that one.  

Senator ROBERTS: Okay. Excess deaths, 13 per cent, in line with the COVID injections—before COVID outbreaks in Queensland and Western Australia—what would make you investigate whether or not pilots are suffering from COVID injection adverse events? Because you don’t do testing on pilots; you rely upon pilots to turn themselves in. What would make you investigate it?  

Ms Spence: The only thing that would make us investigate is if there was an adverse reaction in the cockpit which could be directly attributed to a COVID vaccination. 

Senator ROBERTS: What if I told you that pilots are telling us that they know of mates who have had adverse events but they won’t speak up for fear of losing their job?  

Ms Spence: I would encourage them to report through the confidential reporting arrangements that I mentioned, both with us and with the ATSB, because we are not getting those reports, and there are mechanisms for them to do that.  

Senator ROBERTS: With pilots losing their jobs, I wonder.  

Ms Spence: As I said, they’re confidential, so they don’t need to report who they work for—but just giving us the information, if that is actually occurring, would be incredibly beneficial.  

Senator ROBERTS: Given that CASA use Austroads fitness to drive as a guideline for recertification for TIA or stroke in class 5 medicals, on what are the class 1 and 2 medical recertification guidelines based, and do they differ from class 5 guidelines? If so, how and why?  

Ms Spence: The standards for class 1 and 2, which is the commercial pilot and the private pilot medical certificates, are based on the International Civil Aviation Organization medical standards for certification for pilots—for commercial and private. They are quite different to the domestic Australian class 5 medical certificate, which is not an ICAO certificate and doesn’t need to comply with those medical standards. So class 1 and class 2 reference the international pilot standards.  

Senator ROBERTS: And class 5—you make up the standards?  

Ms Spence: Class 5 medical standard was developed through really extensive consultation through technical working groups with both doctors and pilots, with operational input from pilots in particular. It also went through a really strong risk assessment process within CASA to determine what those standards should be, mapped against the risk treatments for the operational restrictions with the class 5.  

Senator ROBERTS: But my question was: CASA developed those standards? I’m not interested in the process. CASA developed those standards?  

Ms Spence: Yes, CASA developed those standards.  

Senator ROBERTS: Thank you. CASA allow airlines to push pilots to the limit as a routine practice. This is facilitated by a concession given to the airlines masquerading as ‘fatigue risk management’. CASA have allowed airlines to use this system as a shield when continuing to roster pilots to fly unreasonably long hours. Do class 5 medical holders and class 1 and 2 medical holders operate in the same airspace?  

ACTING CHAIR: What are you quoting? I think the witnesses would like to see the source of that quote.  

Senator ROBERTS: I’m not quoting from anything here. My research assistant—  

ACTING CHAIR: I thought you were.  

Senator ROBERTS: No, I’m not quoting.  

ACTING CHAIR: Okay.  

Senator ROBERTS: I’m just quoting the fatigue risk management title.  

Mr Marcelja: So, for the record, we don’t agree with the statement you just said.  

Senator ROBERTS: Okay. Do class 5 medical holders and class 1 and 2 medical holders operate in the same airspace?  

Ms Spence: Yes, they do.  

Senator ROBERTS: Thank you. Is a class 5 medical holder a single pilot operation?  

Dr Manderson: Yes, it is.  

Mr Marcelja: Yes. 

Senator ROBERTS: Okay. You had some doubts, Dr Manderson?  

ACTING CHAIR: I think they answered the question.  

Dr Manderson: Sorry, only because I felt it was self-evident that—but, yes, it is.  

Senator ROBERTS: Okay. Thank you. So, if a class 5 medical holder with a recent history of stroke or TIA after four weeks of grounding is back in an aeroplane at the holding point at an airport and has a relapse, his or her aircraft taxis out in front of the landing heavy jet fully laden. Class 1 and 2 medical holders can operate with multicrew and autopilots as well as current pilots repositioning as passengers in the cabin on numerous flights. Class 5 pilots have no back-up. Is that correct so far?  

Ms Spence: Senator, I— 

Mr Marcelja: Perhaps you could repeat the question. I’m not sure what the question was in that.  

Senator ROBERTS: We’ve got a heavy laden jet coming in to land with class 1 and 2 medical holders, with other back-ups on their position, and we’ve got a class 5 just about to go in front of the path and they have a relapse.  

Ms Spence: It feels like you’re describing—without being derogatory—a weekend warrior landing in the same place as a large commercial air transport operator, and I’m just trying to—  

Senator ROBERTS: Okay. Let’s continue then. We’ll get on to your weekend warriors. What value does CASA place on the designated medical examiner’s ability to diagnose and recertify pilots? And what situations require CASA to intervene with their diagnosis?  

Dr Manderson: So the designated aviation medical examiners are absolutely fundamental to us being able to make safe decisions about issuing medical certificates. They are the doctors that perform the examination and interact with the pilots and air traffic controllers at every medical certificate renewal application. We trust their assessment as clinicians as to whether or not there is any medically significant or safety relevant medical condition present in that pilot or air traffic controller applicant. We take their clinical information and their advice when we decide whether or not to issue a medical certificate.  

Senator ROBERTS: Why then is CASA advocating self-certification for class 5 medicals—as I understand it?  

Mr Marcelja: We are not advocating. What we’re presenting are options for different types of operations. So a pilot that chooses to operate with a single passenger in a light aircraft can choose a class 5 certificate or they can choose any other certificate. So we’re not advocating any particular medical. We’re creating options and different pathways for different pilots in different circumstances, and those circumstances are adjusted based on risk and the level of medical certification.  

Ms Spence: This is a matter that has been under debate for a number of years, around CASA being a proportionate regulator. Under the class 5 medical, we put restrictions on the way you can operate, therefore you can operate within those constraints and then we will review to see how that’s working over time. We’re monitoring it closely to make sure that we’re auditing people’s self-declarations and the like. So I think people do expect us to be a proportionate risk-based regulator, and I think the class 5 medical is an example of how we can do that.  

Senator ROBERTS: That’s what I’m exploring here. I’m trying to understand. I’m not a pilot. Considering CASA AvMed can override opinions of consulting physicians and specialists during the medical renewal process, how could the view of a CASA AvMed doctor come to its own diagnosis of an individual pilot in the absence of face-to-face consultation and overrule the opinions of independent specialists and consultants? Is that possible?  

Dr Manderson: The aero-medical decision-making process is more than and different to the clinical decisionmaking process. The medical assessment process that we’re required to follow by the Civil Aviation Safety Regulations and the ICAO standards and recommended practices is that we take all of the advice that is available from all of the clinicians—including their expert opinions, the investigations and reports that are available, the medical examination from the DAME—and we apply that information against the medical standard for medical certification. The key difference is that the medical specialists who are seeing the patient and the patient pilot or controller are performing an assessment of the medical status of that person as a clinician for diagnosis and management, not for aero-medical risk assessment and not for medical certification processes. So it’s quite a different role and a different process. We consider their advice, but their advice is about the condition and its disease and severity, not about its safety relevance for medical certification.  

ACTING CHAIR: Senator Roberts, we need to break for dinner. Are you close to finishing?  

Senator ROBERTS: We might put these on next Senate estimates.  

ACTING CHAIR: We are going to release CASA now. Thank you very much. 

I was disappointed in the Minister’s response to my questions about the implications of the QLD Supreme Court judgement on the COVID ‘vaccine’ mandates. I expected more clarity and less deflection from the Minister. These decisions were made by the Liberal, Labor and Greens parties, there can be no avoiding the fallout form their actions across the COVID period.

While the ruling was made on the basis of the human rights act in QLD, identical provisions are in place in Victoria and the ACT, suggesting the decision is not just a QLD issue. The government is arrogantly ignoring the reality of the situation and failing to read the room when it comes to this topic.

People have had enough of high-handed, out of touch government. One Nation is calling for the Royal Commission into our COVID response to be announced right now!

Transcript

I take note of Senator Gallagher’s answer to my question on the Queensland Supreme Court’s decision. The court found measures relating to COVID were mandated on a number of Queensland workers without adequate consideration of their human rights as required under the Queensland Human Rights Act. Identical human rights provisions apply in Victoria and the ACT. So certainly there is the probability of the same or similar decisions being made in other jurisdictions.  

I’d hoped the government would be fully aware of the implications of this decision. I was disappointed. The minister deflected and failed to address the substance of the question, so here are some more reasons the minister should get clarity on this issue. An employee who is fired as the outcome from a vaccine mandate can sue the employer, which may be the government, for wrongful dismissal. An employee who took a vaccine to keep their job as a result of a vaccine mandate, who is now vaccine injured, can sue for damages. Class-action lawsuits will result from this decision. The Commonwealth will be as much in the firing line as Victoria and Queensland.  

It’s not just mandates. Evidence has been presented over the last few months that closing schools and denying children education has caused a permanent drop in children’s educational potential and medical health—permanent harm. Last week, a landmark study of 99 million people including Australians found the injections caused an increase in blood clots, brain injuries and heart disease of up to 600 per cent. These injuries are legally actionable. Whether it’s over mandates, vaccine injuries, education or business closures, victims will be joining class-action lawsuits sooner rather than later.  

All levels of government in Australia made terrible mistakes during COVID. Only a royal commission has the powers and the resources to decide what mistakes were made and how the victims of those mistakes can be fairly compensated. This will be expensive, yet failure to act through a royal commission will create a running sore on public administration for a generation. Only an objective royal commission will restore trust in governments and in the healthcare sector. 

We’re told in the media that ‘vaccine’ mandates are over, yet my office hears from many Australians who are refused employment or threatened with being sacked from their jobs unless they take two, sometimes three jabs. What is the current guidance on mandates in the health sector? Department of Health has no particular view and says it can be the employer’s individual decision — there is no national policy or vaccine mandate in place. The Minister has not heard of anyone, including nurses, being sacked recently.

The terms of reference inquiry for a potential COVID Royal Commission involved witnesses who gave this testimony. Despite an alarming shortage of nurses and other healthcare workers, skilled and willing staff are being rejected for their decision based on informed consent. We hear from many healthcare workers and others from across Australia who are still faced with the ‘no jab, no job’ discrimination to this day.

This looks very much like the rule of “hear no evil, see no evil, speak no evil” is being applied by the Minister and the health department. Until they take responsibility and offer a position around employers’ choices over applying mandates there will continue to be a ‘free for all’ on the use of coercion and discrimination to the detriment of individuals and our health care services.

Transcript

Senator ROBERTS: Turning to vaccine mandates—COVID injections—while the media are being fed a line that vaccine mandates are over, my electorate office is getting reports from health workers who are being refused re-employment for not having two COVID injections. What is the health department’s current guidance on vaccine mandates for employment in the health sector?

Prof. Singer : Apologies, Senator. Could you—

Senator ROBERTS: Do you want me to repeat the question?

Prof. Singer : Yes, please.

Senator ROBERTS: While the media are being fed a line that vaccine mandates are over, my electorate office is getting reports from health workers who are being refused re-employment—some have even been sacked in the last two weeks—for not having two COVID injections. What’s the health department’s current guidance on vaccine mandates for employment in the health sector?

Prof. Singer : I’ll just need to look that up. I believe that there may be some in relation to aged care, but we don’t have any particular view on mandates generally. Obviously, they are individual agreements between employers and employees. There is no national mandate as such, to my knowledge.

Senator ROBERTS: Does it bother you, Minister, that there are some state health departments, including Queensland, where nurses are being sacked for not having their two injections and for choosing to go on their informed consent?

Senator McCarthy: I’m unaware of that. Of course, it would be a concern that they can raise in each jurisdiction. But, as the Acting Chief Medical Officer has said, there is no national policy in place on that.

Senator ROBERTS: Let’s move to good manufacturing practice. I have just two questions left. At the last estimates, I tried to get to the bottom of whether every batch of Pfizer COVID injections was made using good manufacturing processes. If they were not, that may explain the huge variance in adverse events between batches. If they were made with good manufacturing processes, there is another cause we really need to understand for the huge number of excess deaths. In your answer on notice, you did not answer the question, but you gave me a list of entries in your manufacturing information database. This is a little confusing, because your answer does not allow me to check good manufacturing process certificates off against batch numbers. What your data tells me is that all of these good manufacturing process certificates were issued as a result of a desktop audit rather than an in-person inspection, which means you took the manufacturers’ word for it based on whatever it was they sent you. Is that correct?

Prof. Lawler : Thank you for the question. I would just highlight that we’ve received these questions regarding the batch testing of vaccines and the associated release a number of times before, and we’ve answered these questions—most recently, I think, SQ23-002145. Those answers are clearly on the record.

Senator ROBERTS: That’s not the one I have. Secondly, there are 44 good manufacturing process certificates for all COVID vaccines, yet there are 410 batches listed in your COVID vaccine batch release assessment. Some of those are duplications and some, admittedly, are for AstraZeneca, but the number seems off. Can you please give me on notice a full list of Pfizer batch numbers and the corresponding good manufacturing process—or is it true that good manufacturing process was only used from the bivalent vaccines onwards?

Prof. Lawler : Thank you for the question. I’m happy to either take that on notice or to return to that under outcome 1.8 when my—

Senator ROBERTS: Perhaps you could take it on notice.

Prof. Lawler : Absolutely.

Senator ROBERTS: Thank you.

In light of Professor Brendan Murphy’s, the Secretary Department of Health & Aged Care, evidence during the June estimates that mandates are no longer justifiable, I asked the Human Rights Commissioner, Lorraine Finlay, for their latest guidance on COVID vaccine mandates.

Commissioner Finlay’s response was that this advice has not changed throughout the COVID response in terms of general human rights principles. What this means is that although governments can restrict individual human rights in an emergency, those restrictions need to be proportionate, non-discriminatory and targeted to risk.

This goes to the heart of the problem. Decisions were made that put Australia onto an emergency footing in 2020. Yet this has dragged on beyond what is reasonable. The response has not been proportionate to the risk of the COVID infection, which the Chief Medical Officer in March of 2021 admitted was low to moderate.

Discrimination remains to this day against those who exercised their right to say no to injections, despite the coercion. We must have a system in place whereby civil liberties are rightfully returned. The Australian Human Rights Commission should be at the forefront of calling for this, yet they appear to be captured, with the exception of Commissioner Finlay, who has come out strongly in support of human rights principles.

Commissioner Finlay is looking forward to the COVID Inquiry that was recently announced, after the Senate approved my motion to establish an inquiry to recommend and report on the Terms of Reference for a COVID-19 Royal Commission. She sees the need not only to look at the economic and scientific impacts and advice that were given throughout the COVID response, but the human cost too.

Transcript

CHAIR: Senator Roberts, do you want to see if you can get some questions done?

Senator ROBERTS: Yes. As the chair said, my questions are fairly short and straight to the point. What is the latest guidance from the commission on COVID vaccine mandates? Where was that published?

Ms Finlay: I would refer you to the answer we gave you in relation to this at the previous estimates. The advice remains the same in terms of the general human rights principles that we rely on in our approach to both
vaccine mandates and all other restrictions that were imposed during the COVID-19 pandemic.

Senator ROBERTS: I must compliment you here and express my appreciation and admiration for your stand on being so clear on the Voice and on misinformation and disinformation. I also want to thank everyone for being here tonight so I could do that. Are you aware of the evidence from the Secretary of the Department of Health and Aged Care, Professor Brendan Murphy, at the previous estimates in regard to COVID mandates?

Ms Finlay: In a general sense.

Senator ROBERTS: On 1 June, Professor Brendan Murphy said – at this stage in the pandemic there is little justification for vaccine mandates. That is the most senior health bureaucrat in the country who said that. There doesn’t seem to be any updated guidance from the commission on vaccine mandates despite the fact they are still in effect at employers and are clearly a breach of human rights that’s not proportionate to any supposed benefit. Why haven’t you come out clearly on this issue?

Ms Finlay: I would answer that in two respects. The first is that the guidance in terms of the general human rights principles remains the same. We are not medical experts. I think we discussed that at the previous estimates. Our advice is based on those general human rights principles where in emergency situations governments can restrict human rights but those restrictions need to be proportionate, nondiscriminatory and targeted to risk. So the advice remains the same because of the general principles of international human rights law that we rely on in informing our views about these things and those don’t change.

Senator ROBERTS: So you as a commission essentially follow blindly? The Chief Medical Officer advised me in March 2021 that the severity of COVID was low to moderate, not severe. So it was not a crisis.

Ms Finlay: No, our advice doesn’t follow blindly. Again, I would refer back to the evidence we gave previously and note that, for example, the most recent TGA advice in relation to their vaccination safety report
repeated the same advice that we discussed at the previous estimates in terms of the benefits of the vaccination outweighing the risks. It’s on the basis of that that the general principles of human rights law then apply.

Senator ROBERTS: I appreciate that you probably haven’t got any latitude to investigate, but the TGA told me at Senate estimates in February, I think, that they did not test the injections. They relied on the FDA in
America, which did not test injections. It relied on Pfizer, which shut down the trial because of the horrendous results.

Ms Finlay: I can’t provide any information on that—

Senator ROBERTS: No, I wasn’t expecting that. I’m just—

Ms Finlay: but I would refer to the second aspect of the answer that I was meaning to get to, which is that we welcome the opportunity for these issues to be explored at the COVID-19 inquiry that’s been announced. Certainly we have made public comments in relation to that inquiry about the need to not only look at the economic and scientific impacts of advice that was given throughout the pandemic but at the human cost of the
pandemic as well.

Senator ROBERTS: That’s refreshing to hear. Thank you.

I’ve been asking for a Royal Commission into COVID for more than 2 years. I am told it’s too early.

It’s now been 4 years since COVID was first found in Wuhan and in Italy and sent the world insane. Lock-downs, business closures and job losses, civil rights violations, coerced vaccination contrary to the Nuremberg Code. Simply inhuman!

Now we have a “scary” new variant, Pirola. Medical evidence provided to me by qualified medical practitioners state that it’s extremely mild and isn’t cause for keeping the COVID scare alive.

I also share the latest research which shows the reason why the “vaccinated” are getting more sick, more often than the unvaccinated, and that this may continue to be an issue for quite some time to come.

Join me for the 4th COVID science update this year.

Transcript

As a servant to the many different people who make up our one Queensland community, tonight, on the fourth anniversary of COVID-19, I ask the Senate to consider the latest scientific discoveries. I’ll then make a request.

The latest variant of COVID-19, called pirola, is now dominating the news cycle and leading to calls for a return of masks, lockdowns and injections, despite there being only 12 cases in five countries. Dr Byram Bridle, a viral immunologist who specialises in vaccines, has published work relevant to pirola, which I will now summarise here.

If pirola were a dangerous virus, it would be easily detected because the increase in suffering and death would prompt testing. With only 12 cases, pirola is not serious. Pirola contains more than 30 mutations on the spike protein, which is what helps the virus enter cells and cause an infection. An accumulation of mutations in the spike protein is exactly the expected result from the poor design of these COVID injections that we’ve been inflicted with; specifically, the targeting of a single spike protein. The approach of targeting a single spike protein encourages the virus to mutate until it finds a variant the shot does not protect against. In this case, vaccination causes mutation. Natural immunity, though, targets multiple components of COVID-19. A person with natural immunity will have both antibodies and T cells that can kill COVID-19 by virtue of recognising things other than the spike protein, so it will be more difficult for new variants to completely evade natural immunity. He continues that Australians with only vaccine induced immunity will be more susceptible to getting infected. That means no immunity. And he says—listen to this quote—they ‘will be prone to more severe illness than people with natural immunity’.

In our haste to force vaccination on every Australian we have weakened the immune systems of our nation and delivered weakened bodies into the hands of the medical establishment responsible for this crime in the first place. In the months ahead, as the medical establishment and their media mouthpieces scare the Australian public into more injections, masks and other manifestations of Soviet control, remember this: pirola is likely less dangerous than any other strain, especially for those with natural immunity. So far it looks like pirola might cause a typical wave of the common cold. It might spread to a lot of people, like most cold-causing viruses do, and for most it will cause mild, if any, disease. Of course, follow medical advice if you’re immunocompromised or unwell. Thank you, Dr Byram Bridle.

Next, David Dowdy, a professor of epidemiology at the John Hopkins Bloomberg School of Public Health, commented:

We don’t want to be sounding alarm bells over a variant that is just as likely to die out as it is to become the next big thing. If we did that for every single variant we’d be sounding alarm bells every single day.

The professor seems to be missing the point that fear is the point, and from fear comes control. If you want to slow the emergence of new variants, like pirola, stop the shots—stop the COVID-19 injections.

While we’re at it, stop manufacturing viruses like COVID-19 in laboratories. Seriously, what else in these labs may escape one day? Surely a royal commission would have to ask that question. It’s now been four years since COVID-19 was discovered in the wild, when three junior researchers at the Wuhan Institute of Virology presented to a hospital in Wuhan with flu-like symptoms. It’s been four years since 14 September 2019, the date Italian medical staff detected what became known as COVID-19. In the years since, the world has gone insane, with lockdowns; business closures and job losses; civil rights violations; coerced vaccination, contrary to the Geneva convention and inhuman; and military on the streets acting on instructions from the Medical Countermeasures Consortium, a military-health joint venture that oversaw the development of COVID-19 as a medical countermeasure, along with the antidote—sorry, the vaccine—produced in case the virus ever occurred in the wild. That’s what medical countermeasures are. Was this unholy military-health alliance responsible for suppressing inquiry into the source of COVID-19 lest it call into the question the wisdom of gain-of-function research? That’s an important question.

The same research was conducted with funding from the US government and supported across USA vassal states, including ours, Australia. I’ve previously spoken about our CSIRO’s involvement in gain-of-function research. Injectables were produced with the claim they could do something a real vaccine can’t do: stop the spread. In the decade before COVID, mRNA vaccines were tested and rejected, repeatedly, for product failure and adverse health outcomes. Then along came a lab engineered virus and those failures were swept aside in what almost felt like a Palm Sunday Hosanna reception. The injections were said to be our salvation, rescuing us from restrictions that governments imposed in order to sell the damn injections—a masterful media manipulation worthy of a royal commission inquiry into the approval and response process that has proven deadly.

Meanwhile, the medical establishment has ignored the obvious signs of injection-induced injury and death. Our medical establishment has responded to each alarming new study and damning data with a routine the internet has dubbed ‘Dr Baffled’. The World Health Organization is currently investigating an unusual rise in severe myocarditis cases amongst newborns and infants in the United Kingdom, one of which resulted in the death of the infant. ‘Dr Baffled’ doesn’t know what’s behind the rise in paediatric myocarditis. He’s baffled! Yet, somehow, he does know for sure that it isn’t the injections, despite myocarditis being a known COVID injection side effect.

In a peer reviewed study published in the Cureus Journal of Medical Science on 20 July, researchers found a correlation between neonatal vaccine doses and infant mortality rates in developed countries. According to data collected from 2019 to 2021, there’s a positive correlation between mortality rates and the number of vaccinations administered to neonates aged from birth to five years. In short: higher vaccine rates were linked with higher infant mortality rates. ‘Dr Baffled’ refuses to even look at this and so many other similar findings. As a result, ‘ Dr Baffled’ remains baffled as to why these children are not thriving on a diet of injected chemicals and genetic material.

In groundbreaking research presented last month, statistician and Luzern University professor Dr Konstantin Beck said:

… miscarriages and stillbirth rates in 2022 corresponded directly to COVID-19 vaccination among pregnant women in Switzerland nine months earlier.

And, he said, vaccine makers and public health officials either knew or could have known this information at the time, if they cared to look.

If they looked, of course, they couldn’t continue to be baffled about the findings. That’s why they’re baffled: they won’t look.

A study of the 500 largest school districts in the USA found that children forced to wear masks in school are on average three times more likely to get sick than those in districts without a mask mandate. Masks amplify diseases found in the wild. A random sample of used children’s masks found pneumonia, meningitis, diphtheria, sepsis and staphylococcus in amplified levels. Schools without masks recorded higher COVID infection rates early in the year, then cases fell away quickly, proving that healthy children only need natural immunity. It’s the best immunity there is. ‘Dr Baffled’ has no comment on the data but assures everyone that masks are safe, contrary to the evidence.

A new paper from the University of Melbourne published in the journal Frontiers in Immunology made the stunning conclusion that the Pfizer vaccine, when given to children, reduces their immune system’s response to other viruses and bacteria, like the bacteria I just mentioned that were found on children’s masks. It reduces children’s health. New information last month shows that Novavax, touted as a protein-only vaccine, free of genetic material, did in fact contain genetic material and a transfectant, saponin, meaning Novavax is a gene-therapy product. Whoops! Another massive scandal the public have not yet been told about. If the media does not speak further on this, I will. The TGA never pulled apart the injectables in their own labs. The TGA relied on what the manufacturers told them was in it so they could maintain plausible deniability of what was in them. A royal commission should short out Professor Baffled and the TGA expert committees on what seems to be a textbook case of malfeasance in office.

Undeterred, the TGA is doubling down. They just announced the removal of pack inserts for all injected products. These inserts used to inform doctors of known side effects and adverse drug interactions. For that reason, printed inserts are a legal requirement, saving the doctor from a web search most would haven’t time to conduct. Typically, when the TGA sees a problem, it hides the problem. Without this information, Dr Baffled will be even more baffled as to why patients keep dying suddenly. On the issue of excess deaths, the latest Australia Bureau of Statistics data shows Australian excess mortality remains at 27 per cent—40,000 Australians are dead this year who should not be dead and nobody in this government gives a damn. No one gives a stuff. One Nation calls on the government to call a royal commission into COVID now and, until that inquiry happens, stop the COVID shots now.

One Nation supports the general principle that students should be able to finish their studies without breaking the bank. The real conversation needed though is the artificial monopoly the medical colleges hold over students in this country.

At a time when Australia is desperate for trained health professionals, medical colleges punitively restrict the amount of places available for students, denying Australians a proper supply and ensuring students have nowhere else to turn. A second look into this practice is needed.

While we’re at it, students that chose not to take the COVID injections need to be allowed to complete their studies or have their HECS debt refunded.

Transcript

One Nation supports the general principle that this MPI proposes, that students should not have to go broke to finish their studies. The medical colleges currently rely on huge numbers of students paying their own out-of-pocket costs and even making thousands of hours of unpaid placements in addition to their studies. The real conversation we need to have, though, is about the artificial monopoly the medical colleges hold over students in this country.

Australia is crying out for health professionals, and the fees to see them are too high for some people. While this is happening, the medical colleges putatively restrict the amount of places available to students, denying Australians a proper supply of trained professionals and ensuring students have nowhere else to turn. We need to have a second look at the medical colleges. And we need to have a look at the universities, who are punishing some people who have completed their academic studies and just need to do their practical courses. The universities are forcing them out because of mandates for COVID injections. That’s inhuman—three to four years work and a contract broken.

The mainstream media tries to falsely paint anti-mandate protesters as extremists. Its the Australian Security Intelligence Organisation’s job to monitor people who are actually violent extremists. They told me what we already know. Protest and political dissent against mandates is completely lawful and it is only a small fringe element who take advantage of the whole group to push violence. The overwhelming majority of anti-mandate protesters are law-abiding peaceful people.

Transcript

Thank you very much Senator Keneally. Senator Roberts.

Thank you, Chair. And thank you all for appearing today. Recent public statements from you indicate ongoing issues of interference by foreign nationals in Australia, including attempts to influence the electoral process. Is this considered to be an ongoing threat from that identified foreign power?

As I said, in my threat assessment centre there are multiple countries. So this threat is real. It happens at all levels of government, local, state and federal. And that threat continues. In fact, espionage and foreign interference is now supplanted terrorism as our country’s principle security concern. And that’s not to take away from the terrorism threat.

Are the identified risks. Well, you just told us they’re serious, very serious.

They are.

Right throughout all levels. From your public, changing the topic slightly. From your public statements, why are so many everyday Australians opposed to mandated COVID-19 vaccinations? They’re opposed to the mandating, not to the vaccinations necessarily. Why are they being monitored?

Well, that’s not my remit. That’s nothing to do with me in terms of whether people are opposed to mandates or want to get vaccinated. That’s not a violent extremism problem that doesn’t fit within my head security. So we don’t monitor or follow those people. If those people also happen to be violent extremists promoting communal violence or politically motivated violence then they would get my full attention. But if they’re not in that category as I said in my speech last week,

“The vast majority of these protestors we’re seeing at the moment are not violent and they’re not violent extremists.”

Mike Burgess, Director General of Security Australian Security Intelligence Organisation, Senate Estimates 14 February 2022

That’s very pleasing to hear that confirms pretty much exactly what the AFP commissioner said just an hour or so ago. But the press has perhaps taken a slant on that. So thank you for clarifying that. And having been at the protests on Saturday, people are just excellent. Why would you consider? Okay. You’ve eliminated that. You said in your recent security annual threat assessment that you do not have a problem with people holding opinions. And would only intervene when these opinions involve promoting violence. You’ve just confirmed that again. What evidence links everyday Australians exercising their right to peaceful protests to being considered domestic terror extremists? I take it that’s a media exaggeration.

Well no, in terms of protest protests, its lawful public dissent is totally appropriate and right for people to do, but actually if people are preparing for or advocating acts of violence then they do fall into my agency’s remit and we will watch them carefully to understand what they’re up to and with our police partners work to stop them from harming Australians.

Yeah. There is a small element just about every group who takes advantage of the group.

There certainly is.

Thank you. No, I don’t need to answer… ask the seventh question. Everything’s covered. Thank you, Chair.

Thank you very much, Senator Roberts.