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WHO Director, General Tedros Ghebreyesus, has conceded the failure of the WHO Pandemic Treaty at the start of the World Health Assembly 77.
This is a great day for those of us who have stood against a global health dictatorship, including myself and One Nation Australia.
Ghebreyesus was a terrorist with the Tigre Liberation Army. While at the helm of WHO, he has actively covered up the rape and sexual exploitation of women in the Congo by WHO personnel, as found by his own investigative commission.
The world has decided that this man and the degenerates at the WHO should not be trusted to lead the next pandemic response. Perhaps by sacking this man and re-empowering the old guard at WHO—doctors who genuinely want to heal and do good—trust in the organisation could be restored.
Additionally, removing the influence of predatory billionaire Bill Gates and his foundation, as well as globalist front groups like CEPI, would also help WHO regain their damaged reputation.
Nations don’t need a Pandemic Treaty to review their COVID performance; they just need the will and courage to scrutinise every aspect and uncover the truth behind the advocacy and fake science. Instead, governments worldwide, including Australia, are avoiding these issues, fearing the loss of sponsorship and protection provided by the crony capitalist world order.
Years ago, I promised to hound down those responsible for the death and destruction caused by corporate cronyism in Australia, and I will continue to do so.
Today is a good day for the resistance. Let this encourage all of us to renew our efforts to bring the guilty to justice and eliminate cronyism from our governance.
UPDATE: 29-May-2025
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 Spence said she was aware AstraZeneca had been withdrawn and that Novavax had also been withdrawn.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.
Queensland residents can’t find a home because there are simply more people than homes. Our hospitals are ramping because there are too many patients and not enough healthcare staff, and the number of kids in Queensland classrooms are rising not falling, despite many parents opting to home school.
The COVID response era actually provided a great opportunity to catch up on building infrastructure while immigration was frozen and people were out of jobs. Instead the government paid people to stay at home and NOT contribute to or build social infrastructure.
I asked Minister Watt, who is a Queenslander himself, if the Government opened the floodgates on immigration without the necessary social infrastructure being ready. His answer confirmed the government has not done the sums on the impacts of our record level of immigration and, quite honestly, is not fit to govern.
Transcript
I move:
That the Senate take note of the answer given by the Minister for Agriculture, Fisheries and Forestry (Senator Watt) to a question without notice I asked today relating to social infrastructure.
For three years, from 2020 to 2022, with the nation mostly out of work, we had an opportunity to catch up on social infrastructure: hospitals, schools, transport, water and housing. Instead, we paid money that could have been used to build those things to people to sit at home and not build those things. It was a trillion dollar wasted opportunity. With a new Labor government in power, the immigration floodgates then opened without the social infrastructure to accommodate the new arrivals. What’s worse is that there are not enough land re-zonings, building applications, approvals and starts to ever make a noticeable improvement in housing.
The Albanese government created a problem it cannot solve. Australia needs to get a refund on that plan we heard so much about from the Prime Minister in the last election because it’s a dud. It’s not up to the minister in his answer to blame the previous government repeatedly. For three years a so-called National Cabinet of Liberal and Labor leaders ran the country, so failure is on both your hands. It’s true that the neglect of social infrastructure goes back through 30 years of Liberal and Labor governments—the uniparty.
The message from the last two weeks of elections in Queensland and Tasmania is simple. Voters worked out the link between immigration and social infrastructure and voters are not happy. Voters are angry with Minister Watt and the Albanese government for creating a housing crisis that’s rapidly escalated to now be a human catastrophe. The public are noticing the disparity between those benefiting from the property market and those falling behind. It now takes everyday Australians on a median salary up to 14 years to save for a deposit for their own home. The housing crisis the Morrison government started and the Albanese government multiplied is disenfranchising the young. The irony is that the Labor government—supposedly, once the party of the workers—is making inequality of wealth far worse. Before the thread of social cohesion unravels in this country, this government must turn off the immigration tap and start building social infrastructure.
Question agreed to.
As a Scientist and former vet school Dean, Professor Rose became concerned that critical information about SARs-CoV2 virus and COVID-19 vaccines was not being reported by mainstream media.
We discussed how the world and particularly Australia changed with the arrival of COVID and how the population seems to have forgotten the drastic restrictions that were put on our freedoms. We also discussed what, if any, lessons were learned.
Reuben received a notice from YouTube that he had “breached community guidelines” and the link to his channel can no longer be accessed.
You can search for more of Reuben’s work here: https://reubenrose.substack.com/ | Sons of Issachar Newsletter | www.inancientpaths.com
It’s time for a Royal Commission into COVID – as recommended by the Senate Legal and Constitutional Affairs Committee Inquiry.
Before the last federal election, Anthony Albanese promised to hold a Royal Commission into COVID, yet once elected into government, he changed his attitude and now seeks to cover up government actions during COVID.
One Nation secured a Senate Inquiry to write Terms of Reference for a COVID Royal Commission. I am proud to say the Committee agreed this was the right course of action and recommended a Royal Commission be called. The Committee also set out an appropriate terms of reference – which are excellent – covering all aspects the public would expect to be examined.
It is time for the Prime Minister to stop shielding bureaucrats, the media and multinational pharmaceutical companies. The Prime Minister is making a mockery of the Labor Party’s legacy. PM Gough Whitlam initiated thirteen Royal Commissions during his tenure, and PM Bob Hawke called for eight. This current Labor government has only called for one, despite public opinion polls indicating over 70% support for a Royal Commission.
It’s time for the Labor Party to prioritise people over its donors in the pharmaceutical industry.
It’s time for the Labor Party remembered who they are.
It’s time for a Royal Commission into COVID now!
Transcript
On behalf of One Nation, I thank the committee and the secretariat for their marvellous work during this inquiry into a COVID-19 royal commission, work that resulted from a One Nation motion. Many submissions were received and witness testimonies taken. The report that Senator Scarr has just tabled is a faithful representation of their evidence and reflects some amazing work by the secretariat, him and the committee.
Australia now has the recommendation that a royal commission into Australia’s response to the COVID pandemic be called, and it has appropriate terms of reference. So what happens now? To this point, the process has been one of which I’m proud. This Senate has held true to its fundamental function as the house of review. The Australian Parliament House website says of the powers of the Senate:
Democratically elected, and with full legislative power, it is generally considered to be, apart from the Senate of the United States of America, the most powerful legislative upper chamber in the world.
It’s time to use that power. Indeed, it’s our duty to use that power. It’s time to remind health care, the military and the bureaucracy: they do not run this country; the Australian people do. It’s long overdue to remind the crony communist establishment: they do not run this country, the Australian people do. And it’s time to restore trust in government and confidence in our healthcare practitioners, hospitals and medications. A royal commission is the only way to get to the truth, punish wrongdoing, praise the noble and set a future direction for pandemic preparedness in which the public can have complete confidence.
Support for a royal commission came from every witness at the inquiry—a rare and overwhelming display of consensus and unity in what has been until now a highly contentious debate. The inquiry submission from Professor Scott Prasser was most helpful in guiding debate around a royal commission. He said:
As then Justice Holmes, who chaired the 2011 Queensland Flood Commission of Inquiry observed there is an expectation in Australia for such inquiries following disasters:
… contemporary society does not countenance a fatalistic approach to such inevitabilities, even if their occurrence is unpredictable. There is an expectation that government will act to protect its citizens from disaster, and that all available science should be applied so that nature and extent of risk is known, and appropriate action taken to ameliorate it—
to protect people. Those who do not learn from history are doomed to repeat it. Remember these facts on Australia’s COVID response: half a trillion dollars was spent, economy and family livelihoods were smashed, freedom and human rights were stolen, and there were tens of thousands of deaths from injections approved yet not tested in Australia, with approval based only on Pfizer’s trial that was cut short after thousands of deaths and without the TGA seeing the patient-level data.
The AstraZeneca vaccine was withdrawn last week. How the hell do the injected withdraw it from their bodies? The department of health still approves AstraZeneca now. Overnight, a peer reviewed journal published proof that the Pfizer vaccine was contaminated with mutant DNA at levels that are hundreds of times higher than safe levels. The Pfizer vaccine must be withdrawn on safety grounds immediately. This is all for a virus which the Chief Medical Officer advised me in writing in March 2021 was of low to moderate severity, less than some past flus, and had transmissibility similar to that of flu. That was in writing. Australia will not stand for repeating our COVID mistakes and COVID deceit.
As I travel through Queensland and listen to everyday Australians, I continue to hear of COVID harms. It’s clear that COVID may be over, yet the harm from our response continues. Businesses weakened during COVID and kept alive with JobKeeper payments are now failing in the recession that inevitably followed the big spend. Victorians have been hit with a COVID tax to pay for the state’s response, a tax making it harder for homeowners to keep their homes in the face of rising interest rates. In turn, rising interest rates are a function of the inflation caused when the Reserve Bank printed $508 billion to fund COVID measures.
Our COVID response affected every life in this country and every corner of our economy. A quickie cover-up whitewash pseudo-inquiry into bureaucratic performance during COVID will not get to the truth of matters into which it’s not even looking. issues like unexplained deaths, which have started to increase again and are currently sitting at around 13 per cent, or 25,000 deaths a year. These are people who should not be dying—young people. In part, these people are dying of the side effects of the AstraZeneca vaccine that Craig Kelly specifically called out in 2021. Our health authorities claimed it was safe and effective until court cases caused AstraZeneca to withdraw the product worldwide, citing a fatality rate of 3.8 per 100,000 cases. Australia bought 56 million doses.
The official death figures from COVID injections are a fiction. Evidence of this is the TGA’s refusal to provide independent verification of their case analysis. Reports of deaths and serious injuries from COVID jabs stopped being made in full early in the rollout. Medical practitioners who reported adverse events were inevitably harassed and threatened with punitive action from the Australian Health Practitioner Regulation Agency, who acted as the pharma police. Their actions in suppressing the truth of vaccine harm must be of special interest to the royal commission.
Pfizer conducted aborted safety testing on a version of the vaccine they never used. The shots they did use were never safety tested, and this was the big lie: that the vaccines were tested and proven safe—a lie. ‘Safe and effective’ was not one lie; it was two. Pfizer are currently settling their lawsuits out of court, but for how much longer, as one successful lawsuit leads to another? Australia offered taxpayer funded immunity on these products. Remember: if criminal behaviour is detected from Pfizer, the immunity can be voided—behaviour like baiting and switching the test vaccines, covering up adverse events in the testing phase and erasing anyone with a serious adverse event from the trials as though they were never a participant. Ghost test sites were used, along with ghost participants who, miraculously, never had an adverse event. Window shifting was employed. Adverse events in person that was single dosed were counted against the unvaccinated, because one is not classified as fully vaccinated until after the second dose. How’s that for deceit? Likewise, even a person who was double dosed had their adverse event counted against the unvaccinated if it occurred within the first seven days for Pfizer and within 14 days for Moderna.
Behaviour like this is why we have royal commissions with powers to compel witnesses and obtain documents that have been hidden behind redactions. There have been 54 royal commissions since the Menzies era. The Hawke-Keating government called eight and the Whitlam government called 13. The Abbott-Turnbull-Morrison government called eight. After so long in opposition, the Albanese Labor government has only found cause to call one. What a compliment to the quality of the last government! In all of that time, only one thing was done badly enough to call a royal commission. You on this side must be so proud!
Prime Minister Albanese has turned his back on Labor Party history and seeks now to cover up for bureaucrats, multinational pharmaceutical companies and crony capitalist companies like Woolies and Coles. These companies implemented onerous staff vaccine mandates, required customers to behave like they were diseased and blasted out pro-vaccine anti-human propaganda over their PA non-stop for three years. It’s no surprise that their share register includes names like BlackRock, Vanguard and State Street. These same names appear in the share register of the pharmaceutical companies that profited from killing people in this country.
These foreign predatory wealth funds appear on the share register of Australian media that contributed unending fear to drive the pharmaceutical response to COVID. The media also policed public opinion, destroying the careers of presenters, medical professionals and politicians, despite those opinions now being proven correct. Even worse, their opinions were known to be correct at the time these brave people were speaking out against the official narrative during COVID. Was COVID an evil exercise in crony capitalism, in racketeering for the benefit of foreign predatory wealth funds, or crony communism? Yes, it was. Those funds have ripped $5 trillion—trillion—from the pockets of everyday citizens around the world in the name of keeping us safe. What an eye-watering transfer of wealth, unprecedented even in wartime. Thanks to COVID, the rich are richer, while everyday citizens struggle with reduced wealth, unprofitable businesses and poor health.
And yet the Labor government refuses to call a royal commission. You don’t care! Is this who the Labor Party has become—protectors of racketeering wealth funds and their parasitic, predatory billionaire owners? Is that it? One benefit of misinformation laws is that they may stop you calling yourselves the party of the worker when you are clearly the party of predatory billionaires—parasites.
Prime Minister Whitlam called 13 royal commissions, Prime Minister Hawke called eight and this Labor government has called one. Talk about not being able to handle the truth. Your position defies history, it defies the will of the Senate and it defies the will of the people. Talk to anyone in the street; they’ll tell you they want this. Your position defies history. I urge the Senate to send a clear instruction to the Prime Minister that his quickie cover-up inquiry has fooled nobody—nobody. It’s time to begin the royal commission; it’s time to care about people, not corporate profits; and it’s time for this Labor Party to remember who they should be. I seek leave to continue my remarks.
The final report from the Legal and Constitutional Affairs Committee regarding the Terms of Reference for a Royal Commission into the federal government’s handling of COVID-19 has been released.
This inquiry was initiated after the Senate passed my motion to establish it, which comes after extensive efforts by One Nation to uncover the truth about Australia’s COVID response.
The good news is that the committee recommends the federal government establish a Royal Commission to thoroughly examine Australia’s response to the pandemic and its impacts on the community. The report includes comprehensive terms of reference, covering all aspects that Australians are keen to see addressed, including the vaccines.
I appreciate the committee’s diligent work and welcome this report. I will address this matter further in Parliament next week.
RECOMMENDATIONS
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)
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
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.
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