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I called on the Senate to support the inquiry into the federal COVID-19 Vaccine Injury Claims Scheme and restated my demand for the people of Australia to have their Royal Commission in COVID.

Australians are dying at a far higher rate than normal. Surely even the pharma industry lobby in the Senate can see that there’s a high probability that the cause, the one thing that has changed in the last 4 years coinciding with the increased mortality, is the jabs that everyday Australians were coerced and bullied into taking.

Why is the Labor Government so afraid of uncovering the truth? If they’re confident it’s not the cause, then shouldn’t they be prepared to have an inquiry into it?

This is an issue of life or death for the Australian people and it needs to be above suspicion. We need honest debate and proper scrutiny to understand why over 30,000 people more than normal have died so far.

In this speech, I go further into messenger RNA “vaccines”, the technology used to protect them and the actual mechanism by which these jabs could be causing the harm we are seeing.

I also talk about the “bait and switch” that was used during clinical trials, which saw trials conducted using the long-established method of using albumin to grow the vaccine. After testing, this was switched out for a new and untested method using a derivative of E. coli bacteria, which multiples much faster but contaminates the vaccine in the process.

During an interview on the ABC, Greg Hunt, the Health Minister at the time, admitted that “The world is engaged in the largest clinical trial, the largest global vaccination trial ever, and we will have enormous amounts of data”.

Where is that data now and what does it really say about our COVID response? The answer will only come from an inquiry. Clearly the Albanese Government and the Opposition do not want you to know.

Transcript

There have been more than 25,000 deaths. That’s more than 25,000 homicides. At Senate estimates hearings last November I produced an independent analysis of Australian Bureau of Statistics data. It showed the unexplained increase in deaths for the period 2022-23—population adjusted, excluding COVID and respiratory deaths—was 13 per cent. The Australian Bureau of Statistics provided data using a different methodology, which agreed closely with my figure. An increase of 13 per cent above baseline on 195,000 deaths in 2022-23 means 25,000 more Australians died than expected. 

Did the novel COVID injections cause all of these deaths? While highly likely, it’s possible they did not. Were enough of these deaths caused by the injections to be of serious concern and to support an inquiry? Definitely yes. A common argument against having an inquiry is the issue that increases in mortality are due to many different causes—cancer, dementia, cardiac conditions and diabetes—so there can’t possibly be a single cause. An inquiry would need to explain this. In the absence of an inquiry, I’ll advance a theory from many credible medical authorities. I’ll do that in a minute. 

The COVID products are not vaccines because they don’t stop people getting COVID. They don’t stop people passing it on to someone else. I call them injections or jabs. The jabs include a segment of messenger RNA, which has the purpose of splicing a new segment into our DNA, which produces a protein to create an antibody to COVID-19. This raises the possibility that disease can be prevented, using mRNA techniques to get our bodies producing antibodies to stop cancer and disease in their tracks. This opportunity to play God has proven so intoxicating that many in our health industry have fallen for it; mRNA jabs are being defended with religious fervour. As with any religious zealotry, those who ask difficult questions like, ‘Why are so many people suddenly dying?’ are being treated in a way that is an afront to parliamentary process and civil government. This issue is life or death. It needs to be above honest debate and scrutiny. 

One potential explanation for increased mortality rates across a wide range of conditions is a scandal known as ‘plasmidgate’. This is technical, so I’ll use plain language and apologise to any specialist vaccinologists listening. Messenger RNA is too fragile to use in a vaccine. To protect the RNA sequence from damage, these COVID jabs use a new technique, wrapping each one in a protective coating called a lipid nanoparticle. This keeps the RNA intact on its journey from your arm to the nucleus of every cell in your body, where the coating helps the RNA enter the cell and bind with your existing DNA. Remember, there are billions of mRNA particles in every jab. 

The manufacturing process is not clean. Fragments of DNA are being picked up in the manufacturing process and getting coated in that protective layer as well, a coating that stops your body expelling the fragment. These fragments are coming from the E. coli bacteria, a derivative being used to grow on the mRNA. Yes, they’re using modified E. coli bacteria as the growing medium for the mRNA in these jabs. 

The clinical trials for this product were conducted using the previous growing method, albumen from eggs. That’s the clinical trials. Yet that was far too slow for Pfizer, claiming the so-called speed of science. So, after the clinical trials were tested, with a conventionally propagated product, Pfizer switched it out for one grown using the much faster E. coli bacteria method. Has E. coli ever been used before as a medium to grow on a vaccine? No, it hasn’t. No, it has not. Was any safety testing done? Well, that would be every person that has had done the jab. That’s where the testing was done, if you’ve had the jab. Now people are dying, and the mRNA vaccine zealots are ignoring the outcome. The crime of the century is that the Australian public have been injected with DNA from E. coli bacteria that was wrapped up in a protective coating and delivered into the nucleus of every cell in your body. 

It gets worse. The latest peer reviewed published data on this shows that, in a third of cases, the cell will not produce the antibody intended against COVID and instead will produce some other antibody—in a third of cases. It’s a process called frame shifting, which means the mRNA does not present itself to your DNA strand correctly and accordingly combines with your DNA in an unintended way before producing an unintended protein antibody. This is going on in people’s bodies right now. What does that mutant protein do to your system? Nobody knows. Here’s the final crime. These mutant proteins are not created in one-third of people; they’re created in one-third of cells, meaning that everyone who was injected with a COVID product has a third of their cells now producing mutant proteins. We don’t know what harm that will cause. The harm varies from person to person. 

Are these proteins now resting in our brain? Are they? We know it can cross the blood-brain barrier into our brains. Are these proteins resting in our hearts, in our livers, in female ovaries, in male testes? Is it turning off our body’s natural cancer defence, resulting in turbo cancers? Highly likely. These are questions, not statements. When some of the most highly qualified medical professionals on this topic are asking questions, there is no excuse not to be investigating when those questions are being asked. It’s time to treat the zealots of the religion of mRNA as the maniacs they are. They played God and they harmed people. They killed tens of thousands of people. They committed homicide—homicidal maniacs. 

As a servant to the people of Queensland and Australia, I support this motion from Senator Rennick, which will find out how bad the damage is, and, once again, I call on the Senate to demand a royal commission into the crime of the century. 

The PRESIDENT: The question is that the motion moved by Senator Rennick be agreed to. 

The Senate divided. [12:18]  

(The President—Senator Lines)  

There’s a long tail to the COVID response that’s affecting a lot of things. There are many changes to the way we work — working from home for example — and the way in which we interact with employees that are a direct impact of the changes made during COVID. The Australian Industry (AI) Group clearly showed in their submission the anxiety levels and the mental health impact on their members and the everyday Australians who work for them. The mixed messaging, the lack of consistent and clear communication made a challenging situation almost impossible to tolerate.

The AI Group made this statement: If we don’t come to grips with the consequences of the sometimes damaging and divisive actions of states to lock down everything from buildings and suburbs to entire states, we ignore the impacts across the community. Their testimony on the disruption to state borders, not just in border communities but to national businesses, makes clear that it was extraordinary. State and territory border closures were so disruptive they should only ever be used as a last resort. Many businesses were impacted also by localised communications and differing ‘rules’ between states which caused chaos.

The Albanese Government’s limited COVID inquiry excludes state governments from its scope. The AI Group feels this is a big exclusion given the fact that state and territory governments were responsible for implementing a lot of the measures which were contradictory and often capricious. The AI Group supports a Royal Commission into COVID with broad terms of reference.

Transcript

Senator Roberts: Ms McGrath, thank you for your submission and also for appearing in person. It’s so much better to have people here in person, when possible. Your submission states: 

If we don’t come to grips with the consequences of the sometimes damaging and divisive actions of states to lock down everything from buildings and suburbs to entire states, we ignore the impacts across the community. 

What are some of the damaging outcomes that support your call for lockdowns to be included as a term of reference? 

Ms McGrath: That was the element that really had the most impact on our members. Our members, of course, are people and, as was the rest of Australian society, they were dealing with the challenges of the pandemic and worrying about their own health. I think we’ve clearly shown in the submission the anxiety levels and the mental health impact on our members and their workforces. The complexity of the shutdowns, the mixed messaging and the lack of consistent and clear communication made a challenging situation almost impossible to bear. 

Senator Roberts: Basically, what you’re saying is that there are enormous economic impacts that possibly could have been avoided—and I think many of them could have been. Those economic impacts led to anxiety and increased mental health problems, as well as economic impacts on employers. Also, you mentioned contradictions. Something that has been said repeatedly across the whole community by individuals and businesses is that each state had different science. 

Ms McGrath: They did. That’s why I referenced the bushfire response. If we think about the language that we use around bushfires, such as ‘prepare to leave’, and even just how we classify, from mild to catastrophic, the nature of a bushfire, we had none of that nomenclature when it came to the COVID pandemic. It meant that whoever was in front of the camera often used terms loosely, such as ‘essential workers’ or ‘authorised workers’. These all had different terms; often they were used interchangeably. It created great confusion amongst our members, who were trying to manage a very stressed workforce. 

Senator Roberts: I will mention that we have here the Australian Health Management Plan for Pandemic Influenza, which was released in August 2019. This is a thick document, so it was comprehensively done, yet it was tossed out of the window and wasn’t even referred to. I think that led to some of the contradictions. Would you like to comment on that? 

Ms McGrath: I’m not aware of that document; I’m sorry. 

Senator Roberts: Let’s move on to another question. The High Court’s decision on the Western Australian border closures, the section 92 judgement, was instrumental in perpetuating border closures and certainly relied on health advice that closures were justified by the health dangers of COVID. Are you familiar with that decision? 

Ms McGrath: Not particularly, but I am aware of the impact of the state border closures. 

Senator Roberts: Basically, it says that border closures are within a state’s constitutional powers, providing that the state’s response is proportionate to the threat. The High Court decided that, based on the medical authorities’ advice, COVID was a serious threat, yet the health authorities at the time knew it was not. In fact, they gave me, in writing, their conclusion that showed that COVID was of low to moderate severity. If you think about the vulnerable that are a very small subset and you remove that, COVID was less severe than many past flus. Those health dangers have now been proven to be overstated, as I said, which really shows that the High Court made an interpretation of section 92 that was, in hindsight, not only not supported by the facts but also contrary to the facts; the High Court was misled. I note that your submission goes to the section 92 judgement, but it doesn’t offer a better way of doing closures. Can you expand on your thoughts around state border closures, please? 

Ms McGrath: As I said in my opening statement, they really should be of last resort. The disruption to state borders, not just in border communities but to national businesses, was extraordinary. The communication often was very localised. Victoria would talk about what was happening in Victoria, not understanding that there perhaps were companies in Queensland that had trucks that needed to come to Victoria; therefore, the message was never conveyed directly to them. The role that the Ai Group played in COVID was to try to gather all these instructions and directives, translate them into easily accessible language and make sure that all our members had access to them, regardless of where they were located. 

Senator Roberts: Do you consider that the responses to COVID were excessively politically motivated? Maybe that was intentional or maybe it was in ignorance. Some states ran focus groups to determine what the people thought was necessary, and yet we, the people, aren’t health authorities. It seemed to be driven by political purposes or political ends in some states, and that might have contributed to the contradictions. 

Ms McGrath: I’m not in a position to comment on that. I think there are many reasons for the contradictions. One is that the people making the directives were very stressed in their own right and so perhaps were not cognitively prepared for that sort of communication. As I’ve said, everyone was making very many decisions on the run. 

Senator Roberts: Your submission notes that JobKeeper benefits were paid to some companies that didn’t need the money; they made excessive profits during COVID and then refused to pay the money back. Is the answer clawbacks to recoup JobKeeper money or is the answer much tougher criteria for JobKeeper, including targeting small and medium businesses over large businesses? 

Ms McGrath: When it comes to JobKeeper, as we said, carefully calibrated support is best. The challenge with JobKeeper is that it was made very quickly and was quite broad based. When it comes to public policy, as you would know, that sometimes has unfortunate consequences. 

Senator Roberts: Your submission mentions mandatory COVID vaccination policies, yet it doesn’t say what about them should be investigated. Where does Ai stand on mandatory injections? 

Ms McGrath: We don’t have a position on mandatory injections; our position is to support members adhering to whatever regulation applies to them. What we found challenging was, again, a mix of communication styles and a mix of messages that came out, which caused a lot of stress in understanding what their obligations were. 

Senator Roberts: Just as a statement, your submission talks about the need for local manufacturing of personal protective equipment and related equipment to remove the need for stockpiling materials that degrade over time. One Nation fully supports that; we cannot be reliant on foreign countries for such products. Has Ai come up with any policy with regard to ensuring that we have the security of our own manufacturing? 

Ms McGrath: Not particularly. We work with ICN in each state and with a number of different local manufacturers in sovereign manufacturing. 

Senator Roberts: One of the responses to COVID from the previous government was to hand out a lot of money. We were warning at the time that this would lead to inflation and, sure enough, it has. We’re still living with the consequences of the COVID response; would you agree? 

Ms McGrath: There’s a long tail to COVID that’s affecting a lot of things. 

Senator Roberts: A long tail to COVID or to the COVID response? 

Ms McGrath: I’m sorry; to the COVID response. There are all sorts of things—as you say, inflation, which is happening globally, but also work from home policies—and changes to the way that we work and the way that we interact with employees that are a direct impact of many of the rules that came through COVID. 

Senator Roberts: On the second page of your submission you state: The existing Commonwealth Government COVID-19 Response Inquiry does include in its terms of reference a review of the responsibilities of state and territory governments and national governance mechanisms, such as National Cabinet. However, it includes the specific exclusion from the scope of the inquiry of ‘actions taken unilaterally by state and territory governments’. Given the fact that the state and territory governments were responsible for implementing a lot of the measures that were contradictory and often capricious, that would seem to be a very big exclusion. 

Ms McGrath: We agree. 

Transcript

Chair: Senator Roberts. 

Senator Roberts: The COVID injections or vaccines raise many questions. The TGA admitted to me in Senate Estimates that it did not test them here in this country but relied on the FDA in America. The FDA in America had already admitted previously that it didn’t test them but relied on Pfizer; and Pfizer’s trials were shut down early because of the number of deaths that they had. So, when you haven’t got something consistent, it puts people under a lot of pressure, not only employees but also employers. That puts you in a difficult position, because not all supermarkets forced their employees to get injected; I think IGA didn’t. But I can imagine a Coles or Woolies employee thinking, ‘I can’t go in the back door to the supermarket, because I’m an employee and must get injected; but I can go in the front door any time I want to and stay for as long as I like as a customer.’ How do you make sense of that? 

Ms McGrath: As I’ve illustrated, there are many complexities, particularly in communication and rules, that really added to the stress of the whole situation, and employers and employees were all coping with the same challenges. 

Senator Roberts: And customers. 

Ms McGrath: And customers. 

Senator Roberts: And sometimes they were in all three roles. Your final comment on page 6 of the January submission says, ‘A root and branch review is required to ensure that governments work cohesively and respond holistically during the next inevitable pandemic, and Ai Group supports any moves towards consideration of appointing a COVID Royal Commission.’ A ‘root and branch review’ is pretty serious stuff; it would be very detailed and comprehensive and would cover everything. 

Ms McGrath: Yes. 

Senator Roberts: Is that because it was so variable and there were so many contradictions and inconsistencies that it just didn’t make sense to many people? 

Ms McGrath: Yes, it didn’t make sense. Sometimes, there would be a minister or health officer making an announcement and we’d wait for the actual orders, and they would not be consistent with what had been announced. We would have to try to find a way to convey that to the government and ask them which directive we should listen to, and then they would try to reverse it. But it was just incredible, I think. 

Senator Roberts: I can empathise with you. I remember watching Yvette D’Ath, the Queensland state health minister, laying out the law in January 2022 or 2023, saying, ‘People in cars must wear masks.’ Someone asked, ‘What about if the driver is by himself?’ and she hummed and said, ‘Yes’. There was no science behind that: sitting alone in a car, with windows up, wearing a mask. These things were not driven by science. 

Chair: Is that a question, Senator Roberts? 

Senator Roberts: It is a statement, backing up Ai Group’s concerns. 

The Consumers Health Forum (CHF) seeks to understand how society in Australia has been impacted by COVID and the COVID response. This not-for-profit organisation was founded approximately 40 years ago and is funded by the Australian Government – as the primary national healthcare consumer organisation under the Health Peak and Advisory Bodies Program.

CEO Dr Elizabeth Deveny seeks to support Australians experiencing ill health as a consequence of the pandemic. She agrees that deferred healthcare needs to be examined in a Royal Commission, as she believes a good COVID response needs to be an enduring one. There needs to be a coordinated response to support unwell Australians to return to health — regardless of whether the cause is from COVID, or the government and health authorities response to COVID.

The CHF seeks a broad and independent Royal Commission into COVID. She says hearing from people impacted by the COVID response will provide Australians with a voice and help restore trust. There will be those who are still suffering trauma or whose lives are still in turmoil. Allowing private sessions will give those witnesses, regardless of their background, an opportunity to come forward and disclose their evidence without exposing them publicly to negative impacts.

The current inquiry commissioned by PM Albanese is run by those who advocated for the very same COVID response the inquiry is supposed to be critiquing. Understandably, Australians need proof of impartiality to have the confidence to trust a Royal Commission. Dr Deveny suggests the selection process should involve the community and build from that point. We need to lift up the voices of health consumers to ensure that the Australian health system meets the needs of every citizen.

Transcript

Coming Soon

Supporting Health Consumers to be Better Informed

In 2019 the government published the Australian Health Management Plan for Pandemic Influenza. This substantial document was the result of 8 years of consultation. When COVID arrived, the government tossed this strategic plan in the bin — just 4 months after it was published.

I asked Dr Elizabeth Deveny, CEO of the Consumers Health Forum (CHF), if her organisation was consulted on this strategic health framework. Dr Deveny will respond to my question on notice.

I then asked Dr Deveny if the CHF is interested in investigating the reporting of adverse events and excess deaths due to the COVID ‘vaccines’. Since COVID ‘vaccines’ were rolled out, excess mortality is around 26,000 above normal annual mortality. The DAEN (Database of Adverse Event Notifications) is a surveillance system that receives reports of adverse events or side effects from medicines, vaccines, biological therapies and medical devices. It’s monitored by the Therapeutic Goods Administration (TGA).

Adverse events, including deaths from COVID ‘vaccines’ were reported to the DAEN — although we know there’s always under-reporting of these events. I outlined for Dr Deveny how official downgrading of approximately 1060 deaths originally tied to these experimental and novel COVID shots meant a large number was removed from the database, leaving 14 deaths attributed to the injections.

Dr. Deveny noted that consumers frequently struggle to find the appropriate channels and methods for lodging complaints about negative healthcare encounters. She believes that the current reporting procedures are not easily navigable for users. Consequently, many incidents involving medication, vaccines, biological therapies, or medical devices go unreported.

The CHF is advocating for improved mechanisms, especially during emergencies, to ensure Australians can easily report concerns about their health. They believe that individuals should be able to express their worries and receive guidance promptly. Both the government and the Australian public need to understand the repercussions of adverse events, as they impact everyone financially. As taxpayers, Australians deserve to comprehend the full effects of health interventions and their outcomes. The CHF supports transparency and is calling for a comprehensive Royal Commission into Australia’s COVID response to empower and inform all health consumers.

Transcript

Coming Soon

Thank you Hoody for your courage in speaking the truth at the second public hearing to set the Terms of Reference for a future Royal Commission into COVID.

“I urge this Senate and I urge this government with these words: Government you must listen. This country is in dire straits. The spirit of this country has been systematically destroyed and I’ve witnessed it firsthand. I’ve done what many of you don’t have the time to do. I’ve been face to face with people who’ve lost loved ones that they know were from vaccine injury. And I don’t know whether these excess deaths are being caused by vaccines or ‘long COVID,’ or whatever else it might be. It could be an additive in food. I don’t know, but nobody else seems to know either and that’s why we must stop. We must investigate. We must do a proper debriefing. We must apply proper human factors. And we must bring the people that I mentioned that have been locked away with censorship, back out of the dark with their data so that we can start healing the people of this country. And if we don’t do that we have neglected an opportunity that will go down in history as one of the greatest human factor failures in the world.”

One thing that has come out of the COVID response is how it’s exposed the pharmaceutical industry to more scrutiny from the public than ever before. More questions have been raised about the Therapeutic Goods Authority (TGA) and our Health Pharmacrats than ever before. Yet, what is the alternative?

In this parliamentary speech, I put it on record that we must look at the influence of pharmaceutical companies on the education system for medical professionals, and the relationships between pharma giants and former health department executives. The toxic, inhuman killer ‘pharmaceutical only’ model is failing Australian taxpayers. People are dying needlessly.

As an example, Albicidin is a natural antibiotic with clear potential to become our leading antimicrobial. It’s proven to not create resistance. Albicidin could be, and most likely is the answer to antimicrobial resistance. There are many others, but they don’t get patented. They don’t receive sponsorship and therefore they don’t get approved.

It’s time for an entirely new medical paradigm. One that puts humans first, not big pharma.

Antimicrobial resistance is the new climate change, allowing for control over agriculture, medicine and household and industrial cleaning, in the name of reducing use of antimicrobials. That’s why an alternative solution, using an antimicrobial that doesn’t cause antimicrobial resistance, is being ignored and quietly buried. It’s to protect globalist profits and to control people – and to hell with human and animal health and safety!

Globalists WANT control. Globalists NEED control to complete their agenda.

Australia needs a customer consumer advocate, or natural product advocate, to advance natural products that can’t be patented, yet are safe and effective treatments — products to be listed under Schedule 4 and offered under the PBS as frontline medicines. Not watered down products sold in supermarkets as complementary medicines so that their efficacy can plausibly be dismissed.

Instead of advancing people-first health care, our Pharmacrats are actively promoting mRNA vaccines and medications to the commercial benefit of big pharma. This is caused by “the patent cliff”, which refers to the expiration of patents on popular drugs, leading pharmaceutical companies to face intense competition from generic drug makers, dramatically reducing their profits. The new mRNA technology allows big pharma to replace off-patent drugs with newly patented mRNA drugs at prices that guarantee their profits for the next 30 years. Our health authorities are actively promoting this solution to the patent cliff, despite the myriad of adverse health outcomes from the mRNA vaccines.

Why? These are important matters that can only be answered by a Royal Commission.

What should not wait for a Royal Commission is a system to incorporate affordable, natural remedies into our health approval process. This could be implemented immediately if the Pharmacrats were interested in providing people-first health care.

Transcript

Where’s the scrutiny on our health authorities? During COVID, drugs were rushed through that would never have been approved on safety and efficacy grounds, such as molnupiravir and remdesivir. Last year, these two inhuman pharmaceuticals cost taxpayers $1 billion. Alternatively, tried and tested drugs that are out of patent could have been used for a fraction of the price. Remember that our authorities and the mouthpiece media called ivermectin ‘horse paste’. The statist Left rushed to demonise anyone who defended ivermectin, because the control side of politics—the so-called Left—loves to follow orders. Ivermectin is a Nobel-Prize-winning antiviral for humans. Over 40 years, it has saved millions of lives. Around the world, it’s now been proven safe and effective as an early-stage treatment for COVID, as it always was.

Our health authorities demonised ivermectin to prevent early-stage treatment of COVID in order to build demand for an untested novel mRNA vaccine. How many died because of the long-term strategy that our health authorities followed and pushed—a strategy to use COVID as a cover to introduce a class of mRNA drugs that the public would have rightly baulked at and rejected? How many died from the side effects of mRNA technology—technology that was not tested in Australia and was not tested off the production line, for which the method of production was changed after overseas testing and approval and the fake trials were at best shambolic and at worst criminally negligent?

Why would our health authorities tolerate this? Simply because of a thing called the patent cliff. Pharmaceutical companies are profitable because they develop a new drug and then get a patent, exclusive sale of the drug for 25 years. Drug companies can afford to put that drug through the approval process because once it’s approved they add the approval cost to the selling price—kerching, kerching!

The system of drug patents has created a $2 trillion industry whose tentacles of influence extend to political parties, who happily accept donations, and to health authorities. Their tentacles extend to the USFDA and Anthony Fauci’s National Institutes of Health, who hold patents on drug processes they license to big pharma in return for hundreds of millions of dollars in personal royalties. Their tentacles extend to the World Health Organization, the United Nations and the World Economic Forum, whose young global leaders sit in this parliament.

This is influence that our healthy authorities cultivate while coveting lucrative careers in the pharmaceutical industry. For example, just eight months after approving Pfizer’s untested COVID injections, Professor John Skerritt, former head of the Therapeutic Goods Administration, the TGA, is now on the board of the pharmaceutical industry lobby group Medicines Australia. This isn’t the normal operation of a free-enterprise system that One Nation would support; this is a cabal of greedy, unprincipled, evil individuals treating everyday citizens as cash cows. They want everything you have for themselves, including your health.

The patent cliff is upon us. There’s increasing urgency—desperation—in the measures being rammed through government. Two-thirds of the revenue is from drugs being sold to you that are out of patent now or will go out of patent over the next five years. That threatens big pharma’s harvesting of humans for profit. Modern drugs, once out of patent, can be made for cents per tablet. India specialises in that. Australia used to, and we can do it again. The patent cliff threatens the entire pharmaceutical industry and stops the ability of chemical pharmaceuticals to do better than they do now, in terms of profit.

From where are the new patents going to come? I’m glad you asked, Mr Acting Deputy President: from mRNA of course. There are 400 new mRNA vaccines and drugs currently under development. Such is the expected volume of these things that two manufacturing plants are being prepared here in Australia. Our health authorities decided to press ahead with mRNA technology to save the pharmaceutical status quo—the pharmaceutical gouging of people to extract exorbitant profits. Patient harm apparently no longer matters.

Last week, a study of 99 million COVID-jab users, including in New South Wales and Victoria, found the product was not safe. The study was published by Elsevier, for more than 140 years the world’s leading scientific publisher and data analytics company. The study showed the following conditions were occurring above baseline levels: brain and spinal cord swelling, up 380 per cent; blood clots, up 320 per cent; Guillain-Barre syndrome, up 250 per cent; and myocarditis, up 278 per cent for Moderna and up 350 per cent for Pfizer. After a second injection, myocarditis was up a damning 610 per cent and pericarditis was up 690 per cent. I told you so four years ago. Many good people warned that COVID products were not tested, that they were experimental, and that forcing them on the general population was an insane, inhuman abuse of government power. Now look at those figures. It’s another area for a royal commission to investigate.

It’s time for an entirely new medical paradigm in this country and throughout the West. Pharmaceutical companies are embracing mRNA as their saviour because it can be patented. They can charge whatever they want for it, and compliant health bureaucrats like our TGA, acting out of self-interest, protect pharmaceutical companies from financial harm. The expert medical advice the TGA relies on comes either directly from drug companies or from advisers who have worked for big pharma, who have accepted research grants or sponsorship from big pharma, or who covet doing so in the future. After all, $29-million Sydney harbourside mansions don’t just buy themselves.

These are things that make for a royal commission. One thing that should not wait for a royal commission is a system for getting cheap, natural remedies into our health approval system. Australia needs an office of the consumer advocate to oversee complaints and the harm bureaucrats cause—bureaucrats who appear incapable of acknowledging odious and obvious adverse events. We need a customer consumer advocate or a natural product advocate to advance natural products that can’t be patented but are safe and effective treatments—products to be listed under schedule 4 and offered under the PBS as frontline medicines, not watered down and sold in supermarkets as complementary medicines so their efficacy can be dismissed. Albicidin, for example, is a natural antibiotic with clear potential to become our leading antimicrobial. It’s proven to not create resistance. Albicidin could be the answer, and highly likely is the answer to antimicrobial resistance.

Antimicrobial resistance is the new climate change, allowing for control over agricultural, medicine, and household and industrial cleaning in the name of reducing use of antimicrobials. That’s why an alternative solution, using an antimicrobial that doesn’t cause antimicrobial resistance, is being ignored and quietly buried: to protect globalist profits and to control people—and to hell with human and animal health and safety! Globalists want control. Globalists need control to complete their agenda.

Take another example: blushwood is an Australian native berry. It was shown, in a 2014 test, to kill skin cancer in just 10 days. Did our health authorities rush to understand this plant and bring a potentially lifesaving medication to market? No; they did not. Another one: conolidine is a natural treatment for severe pain. Ignored! Natural remedies include cannabis. Senator Pauline Hanson has led way, advocating for medicinal cannabis since 1996. I joined her, and now there are others.

A recent paper pointed out that natural products work differently to chemical products, yet our system for understanding and testing substance efficacy is geared to chemical drugs. The paper and system offer a new way of measuring efficacy that confirms plants like cannabis and conolidine do work, and explains how they work. The truth is this: currently only when a product is patented and presented as the TGA on a plate, ready for the TGA’s rubberstamp, does it enter our pharmaceutical system. I urge the Minister for Health and Aged Care to introduce a consumer natural products advocate to provide much needed supervision and accountability over our health authorities. Failing that, I ask the Greens to consider if the agency they’re establishing with the Legalising Cannabis Bill would be better suited to handle natural medications in general—those that the TGA refuse to handle in addition to cannabis.

I’m not offering medical advice on the examples I’ve used in this speech; I’m asking why the health department and medical schools first response is to the scalpel and the prescription pad instead of natural medications that cost a fraction of the price. We must have an independent office in the TGA with the budget to sponsor natural alternatives through the safety, testing and efficacy stages, and to have these promoted to doctors who most likely have never even heard of them.

We must look at the influence of pharmaceutical companies in the education system for medical people, in their relationship with former health department executives and their influence through advertising and sponsorship. The toxic inhuman killer ‘pharmaceutical only’ model is failing Australian taxpayers. People are dying needlessly. Stop so-called health authorities committing homicide, child homicide, infanticide. As a servant to the people of Queensland and Australia, I say call a royal commission now and make an immediate start on the obvious reforms to our health administration that we need.

Many Australians have lost trust in governments at both state and federal levels, and we’ve lost trust in health authorities. Last parliament the Select Committee on COVID-19 stated ‘a royal commission be established to examine Australia’s response to the COVID-19’. That was two years ago. During his election campaign, Prime Minister Anthony Albanese promised the Australian people a COVID Royal Commission. He and Minister Gallagher, who chaired the committee, have both broken their promises.

The Government has clearly chosen to cover-up for the failure of our health authorities to apply human rights to our COVID measures. A genuine party of the worker would be protecting workers against the billionaires who profited from COVID.

The Albanese government must restore trust and commit to a royal commission now. The royal commission could easily commence as soon as the current Senate’s inquiry into appropriate terms of reference defines those terms — an inquiry One Nation secured. I promised to hound those responsible down and I will keep that promise.

Transcript

Today the Queensland Supreme Court ruled vaccine mandates for Queensland’s emergency services workers to be unlawful. What a victory for the Australian people! It’s a victory that reaffirms the need for a full royal commission into Australia’s response to COVID. Everyday Australians have lost trust in governments at both state and federal levels, and we’ve lost trust in health authorities. Recommendation 17 of the report of the Select Committee on COVID-19 stated ‘a royal commission be established to examine Australia’s response to the COVID-19’. That was two years ago.

During his election campaign Prime Minister Anthony Albanese promised the Australian people to hold a COVID royal commission. He and Minister Gallagher, who chaired the committee, have both broken their promises. Appearing to have something to hide looks terrible for the government. It is terrible for the government. The public realise that our Prime Minister and his administration cannot be trusted to keep their word.

Today’s Queensland Supreme Court ruling is encouraging for everyday Australians who’ve lost their source of income. Businesses were forced to lay off their staff unless they complied with the draconian policies, and many industries are still suffering the consequences of having to fire unvaccinated staff. Our nurses, teachers, police, firefighters and paramedics, along with other Australians, deserve to know where things went wrong and why the government turned against them. One simple green tick was the difference in being able to attend school, go to work, move around, socialise and exercise—one green tick that took our rights to freedom, life, privacy and movement.

The Prime Minister must now realise that, if he takes these things from the people, trust goes with them. The Albanese government must restore trust and commit to a royal commission now, to commence as soon as the current inquiry into appropriate terms of reference defines those terms.

The Queensland Supreme Court said there was an abuse of process and that they did not consider the loss of human rights fundamental to Australian democracy. 

Remember when Ivermectin was called a horse paste and they said humans shouldn’t even take it?

Now the World Health Organisation is handing it out to a million humans. 🤷

In January, the Senate held a committee inquiry into appropriate Terms of Reference for a Royal Commission into COVID. This is the Royal Commission the Prime Minister promised during the election campaign, which Senator Gallagher also promised. Instead the Prime Minister called a review of the government’s response, which excludes state and territory responses.

Many have slammed the Prime Minister’s COVID review panel as a “toothless tiger” and support a Royal Commission instead. Doctors, unions, human rights lawyers, vaccine injured, and Royal Commission experts were among the witnesses who provided submissions and gave evidence at the Senate inquiry tasked with proposing Terms of Reference for a future COVID Royal Commission.

Why did the Government Health Department not partake in this inquiry? Could it be to avoid scrutiny from the Committee that would result from making a submission? Judge for yourself.

Transcript

Senator ROBERTS: The department and its agencies did not make a submission to the Senate inquiry into appropriate terms of reference for a possible future royal commission into COVID. I would have thought, Minister, that the department that ran our COVID response would be the first to put forward its position on the matter. Why the silence? Is the department hiding from committee scrutiny? 

Senator McCarthy: We do have an inquiry underway—an independent one—looking into COVID, so I reject outright your question. 

Robodebt had a Royal Commission called three months after Anthony Albanese was elected.

Four years after we first heard of COVID and two years after Albanese was elected, we still don’t have a COVID Royal Commission.

Is PM Albanese only interested in “transparency and accountability” when it’s politically convenient for him?

The Senate inquiry to draft terms of reference for a future COVID Royal Commission is having its first public hearing today (Thursday, 1 February 2024) in Canberra.

This committee will report on what the appropriate terms of reference will be to give all Australians a say and have a fully empowered Royal Commission into the COVID mismanagement.

Panel at Inquiry

  • Institute of Public Affairs (Submission No. 14)
  • Australian Institute for Progress (Submission No. 39)
  • Redfern Legal Centre (Submission No. 9)
  • Australian Human Rights Commission (Submission No. 18)
  • Civil Liberties Australia (Submission No. 13)
  • People’s Terms of Reference (Submission No. 45)
  • Nurses Professional Association of Queensland (Submission No. 46)
  • Australian Nursing and Midwifery Federation (Federal Office) (Submission No. 46)
  • The Royal Australian College of General Practitioners Ltd (Submission No. 41)
  • Suicide Prevention Australia (Submission 21)
  • COVERSE (Submission 34)