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This is my seventh update on the fallout from our ill-considered, dangerous, and criminal response to COVID-19. The truth is becoming clearer with every new study and every new piece of data.

Australia and New Zealand responded to COVID with measures designed to force mass vaccination, resulting in enormous financial gains for pharmaceutical companies. This money flowed through to shareholders—the world’s most predatory billionaires.

It’s terrifying that the entire situation—from the development of the COVID virus to the implementation of COVID measures, including the vaccines—was one giant fundraiser for the world’s wealthiest individuals. Yet that IS the truth!

Let me be clear: those who died from COVID died from a man-made virus. It was developed using gain-of-function research to be more deadly and more contagious than the original SARS virus, which was the starting point for the development of COVID. The virus was then “sold” to the public as the unfortunate result of human interaction with pangolins at a wet market in Wuhan, China.

It’s concerning that so many believed that fanciful story—an over-trust in authority resulting in a medical tragedy that’s still unfolding, as shown in new peer-reviewed and published studies.

Transcript

The New Zealand Royal Commission of Inquiry into COVID-19 Lessons Learned invited several former ministers in New Zealand responsible for the damaging, inhuman and fatal COVID response. These were Jacinda Ardern, the former prime minister; Chris Hipkins, the former health and COVID-19 response minister and current Labour leader; Grant Robertson, the former finance minister; and Ayesha Verrall, the former health minister. All four refused to testify, instead choosing to provide the Hollywood version of their actions in writing, avoiding cross-examination. Jacinda Ardern went so far as to call the royal commission a witch-hunt. One Nation calls it accountability. To refuse to be held to account for their actions is a signed confession of wrongdoing. Australia and New Zealand reacted to COVID with measures designed to force mass vaccination at huge financial benefit to pharmaceutical companies. This money flowed through to shareholders who are the world’s predatory billionaires. It’s terrifying that this entire thing, from the development of the COVID virus to the COVID measures, including the vaccine injections, was one giant fundraiser for the world’s wealthiest people. Yet that is the truth. 

We know COVID itself is a man-made virus developed under Anthony Fauci with funding from the United States’s NIH, National Institutes of Health, administered through Peter Daszak’s EcoHealth Alliance. The research was conducted first in the USA and then moved to the Wuhan Institute of Virology from 2014, where it escaped in a lab leak in September 2019 before development was completed. Documents released through the FBI and others prove these facts. This is why the amazing United States secretary of national intelligence, Tulsi Gabbard, announced the opening of a criminal investigation into Anthony Fauci and his cronies. I wonder if Ms Ardern considers that a witch hunt. The wheels of justice turn slowly, though they do turn. Ms Ardern can stare down a royal commission now, yet the truth is coming out. 

It’s important to note that in its 2020 press release Australia’s own CSIRO confirmed it was involved in this gain-of-function research. Last February, a new paper was published through CSIRO Publishing entitled ‘Impacts of long COVID on disability, function and quality of life for adults living in Australia’. It found that people with long COVID reported worse disability than 98 per cent—almost 100 per cent—of the general Australian population. A total of 86 per cent those with long COVID met the threshold for serious disability compared with nine per cent of Australians overall. Complex areas like housework and socialising were badly impacted. People could often meet basic needs, yet their ability to contribute to their homes, workplaces and communities was limited. Quality of life was badly affected. Energy levels and social life were the most impacted, reflecting how fatigue and brain fog affect activities, relationships and connections. It is without a hint of irony that the CSIRO published a study showing health damage resulting from the virus they helped create through their support for gain-of-function research. All the evidence we have at the moment suggests long COVID can come from exposure to COVID or from the vaccine, the injections, the shots, and from some batches more than others. This is because for the first year the COVID shots were not made using good manufacturing processes, so batch variation was enormous. 

Almost immediately when the virus appeared, we knew that COVID was the product of gain-of-function research. Nobel Prize winning virologist Luc Montagnier sequenced COVID in April of 2020 and found unmistakeable evidence human intervention, including the inclusion of a large segment of the HIV virus. Luc should know; he won his Nobel prize for discovering the HIV virus. The bat virus was spliced in to confuse the human body’s immune system into producing in the wrong immune response to make the virus more deadly, deliberately. Then, for good measure, they spliced in most of the HIV virus to make it more contagious. Let me be clear. Those who died from COVID died from a manmade virus developed using gain-of-function research to be more deadly and more contagious than the original SARS virus which was the starting point for the development of COVID. Then the virus was sold to the public is an unfortunate outcome of human interaction with pangolin animals in a wet market in Wuhan in China. It’s concerning that so many believe that fanciful story and overtrust in authority, resulting in a medical tragedy that continues to unfold in new peer-reviewed and published articles. 

Here are the latest such articles. Chen and others say mRNA injections cross the placenta and reach the fetus. mRNA-1273 crosses within one hour, accumulates in fetal organs, translates into spike protein and persists after birth. Thorp and others say CDC and FDA safety signal thresholds were breached for 37 adverse events following jabs in pregnant women, including miscarriage, stillbirth and fetal arrests. Karaman and others say mRNA shots destroy 60 per cent of a woman’s egg supply, known as primordial follicles. Manniche and others, on a sample set of 1.3 million women, found 33 per cent fewer successful pregnancies in women who had the shots. Freiberg and others, on a sample of 493,000 people—almost half a million people—found a 23 per cent increase in autoimmune disease post shot. 

Did anyone hear about this study conducted from the United States Centres for Disease Control and Prevention epidemiologist Dr Feldstein, published in the Paediatric Infectious Disease Journal, an Oxford University Press peer-reviewed publication? Amongst children aged six months to four years with no prior COVID infection, those who received the Pfizer-bioNTech mRNA shots were 159 per cent more likely to get infected and 257 per cent more likely to develop symptomatic COVID-19 compared to unvaccinated children without prior infection. This study from the US’s own CDC clearly shows that a COVID shot in young people has negative efficacy. It makes children more likely to get COVID, and, when they do, they experience worse symptoms. That study has resulted in the FDA and now Australia’s TGA at long last announcing the end of COVID vaccination for children, after they told us it was essential. Add that to the mental health damage, developmental delays and academic damage done to children during lockdown, and the picture is scandalous. This is criminal. This is inhuman. 

In O’Keefe Media’s recent hidden camera video, Johnson Johnson’s lead scientist in regulatory affairs, Joshua Rys, admitted the typical clinical process was abandoned for the COVID-19 vaccine. J J knowingly bypassed standard testing protocols under pressure from the Biden government. Joshua said: 

This was just, ‘let’s test it on some lab models … and just throw it to the wind and see what happens. 

He acknowledges that the public was not informed about the shortcuts, which were not acknowledged. Did the TGA know that there was no proper safety testing on the J J product before it was given approval in Australia? While public officials claimed the vaccines were ‘safe and effective’, Rys pushed back saying: 

There’s no proof. None of that stuff was safe and effective. 

He added that the industry relies on a benefit-to-risk trade-off to justify product launches. What this means is that the product is justified if it helps more people than it harms. In that scenario, harm is tolerated. If the pharmaceutical company has its thumb on the scale, making harm less and benefit more, then the faulty product makes it to the market. That’s exactly what happened with the COVID products and 20 other products, like Remdesivir, that were approved in Australia. 

Now the latest instalment in Frankenstein science is upon us. Listen to this. Self-amplifying RNA vaccines—saRNA—are being tested. These are shots which replicate inside the human body after injection, turning our bodies into genetic material production units which shed on those around us. This is uninformed consent to vaccination taken to a whole new level. A paper published in the peer reviewed Journal of Clinical Medicine found that the COVID-19 replicon saRNA injections caused severe blood abnormalities in 93 per cent of trial participants. Symptoms include increased risk of internal bleeding and suppressed immune cells, which raises infection risks. Renowned American cardiologist Dr Peter McCullough last week commented on saRNA technology, saying: 

Vaccinologists have made a critical error in the design of genetic vaccines. Injection of the genetic code for any foreign protein including parts of viruses causes the body to respond with an immune attack against its own cells. 

This leads to intense vaccine injury syndromes all through the human body 

He said: 

Giving the vaccines their own ‘life’ with the ability to reproduce themselves is inhumane, reckless, and from the outset, should be flagged as dangerous and potentially lethal to the recipient. 

COVID vaccines were released without proper testing and caused 1,200 deaths in testing alone, in Pfizer alone. Pushing COVID shots killed tens of thousands of Australians—homicide. If saRNA shots are pushed, it will be genocide—deliberate. Those responsible for COVID have not been held to account, yet now they plan to turn every person and every animal into a genetic material production facility. I have now given seven of these COVID updates, 70 minutes of proof—scientific proof, medical proof—that we must investigate this criminal enterprise, or this next generation of Frankenstein science, the saRNA, will kill and maim huge numbers of Australians. 

Dengue fever is a viral illness spread by the Aedes aegypti mosquito (known as the dengue mosquito in north Queensland). The dengue virus is not endemic in Australia, meaning the virus is not normally present in Australia.

Dengue fever outbreaks begin when someone is infected with dengue overseas and arrives with the virus in their blood. This is referred to as an imported case. When a local Aedes aegypti mosquito bites an infected person, it in turn becomes infected with the virus and can then transmit it to others through subsequent bites. These instances are known as locally acquired cases.

The dengue virus does not spread directly from person to person.

Catching different types of dengue, even years apart, increases the risk of developing severe dengue. Severe dengue causes bleeding and shock, and can be life-threatening. There have been deaths in Queensland from severe dengue. This is why a vaccine is problematic, because that relies on giving the subject the disease.

About Oxitec and Their Process

Oxitec’s genetically modified mosquitoes work by releasing sterile males into the wild to mate with females, which results in offspring that die in the larval stage. Oxitec’s mosquitoes are engineered with a self-limiting gene that produces a non-toxic protein that prevents their offspring from surviving to adulthood. The protein, called tTAV, disrupts the cell’s ability to function and prevents the insect from developing normally.

The gene can be switched off using amoxicillin, which allows the factory to breed the mosquitoes, then once in the wild, the amoxicillin wears off and the gene starts producing the protein again.

In short – it’s gene editing, hence the need for the application to the Office of the Gene Technology regulator.

Our CSIRO is a proponent | https://www.csiro.au/en/news/all/news/2024/december/csiro-oxitec-to-tackle-disease-spreading-mosquitoes-threatening-mainland-australia

“Launched today, Oxitec Australia is a collaboration between CSIRO, Australia’s national science agency, and UK-based Oxitec Ltd, the leading developer of biological solutions to control pests.“

And look who is running the show – “Professor Brett Sutton, Director of Health & Biosecurity at CSIRO, said Oxitec Australia is now seeking partners to accelerate its activities and product development in Australia.”

When I said it was a template, this is confirmed in the CSIRO press release:

“This technology platform could also be used to develop solutions for a wide spectrum of pests that threaten livestock and crops and our food systems.”

Oxitec are running field trials on a fall armyworm with the same gene added, which is a moth not a mosquito. And it’s our money going into this so Estimates is fair game:

“Oxitec Australia is also developing an Aedes albopictus (Asian tiger mosquito) solution, with funding from CSIRO, to help prevent a major invasion risk to mainland Australia. “

Mosquito Performance in Brazil

Oxitec launched a year-long field trial in Indaiatuba, Brazil in 2018. The trial involved releasing Oxitec’s Friendly™ Aedes aegypti in four communities. The trial’s results included an average of 89% peak suppression in two communities treated with a low release rate of mosquitoes according to Oxitec. Brazil’s Dengue rate was low in 2018, and jumped up in 2019 and later. The locals are claiming a connection but there is no science around what that connection could be.

Gates Foundation however washed their hands of the Brazil Dengue escalation with this statement:

“A spokesperson at the Gates Foundation told AFP that the foundation ‘does not fund any of Oxitec’s work involving Aedes aegypti mosquito release in Brazil.’ 

NOT exactly a debunking of the controversy.

People are asking if the explosion in Dengue in Brazil the year after the trial was related, especially when the same thing happened after a similar trial for Zika. It is a question that should be addressed, although I do think it is not connected.

Florida 2021 – Nothing Went Wrong

Oxitec ran a controlled release in Florida in 2021. A kill rate of 90% was proven, with no known unintended consequences. HOWEVER, there was an increase in Dengue the following year and the same thing happened with the Zika test in Brazil. The reason this isn’t related is the genotype:

“We documented an unprecedented number of travel-associated and locally acquired DENV-3 cases in Florida during May 2022–April 2023; circulation of the DENV-3 genotype III was recently identified in the Americas. Our investigation illustrates that local transmission and spread in Florida was limited, despite multiple introductions from outside the country. Sequencing and phylogenetic analysis revealed that cases were from the same DENV-3 genotype III lineage and were highly related to one another and to cases identified in Puerto Rico, Arizona, and Brazil.”

https://wwwnc.cdc.gov/eid/article/30/2/23-1615_article

So the outbreak was not spontaneous in the area of the trial, but was introduced from outside.

Dengue Vaccine and the Philippines Scandal

Sanofi Pasteur owns the Dengvaxia® vaccine – the first licensed dengue vaccine and available in more than 20 countries. It is registered with the Therapeutic Goods Administration (TGA) in Australia, but is not currently marketed here.

WIKIPEDIA: “The Philippine Department of Health began in 2016 a programme in three regions to vaccinate schoolchildren against dengue fever, using Dengvaxia supplied by Sanofi Pasteur. On 29 November 2017, Sanofi issued a caution stating that new analysis had shown that those vaccinated who had not previously been infected with dengue ran a greater risk of infection causing severe symptoms. On 1 December 2017, the Philippine DOH placed the programme on hold, pending review. Over 700,000 people had received at least one vaccination at that point.[11][12] Since the announcement by Sanofi, at least 62 children have died, allegedly after receiving a vaccination. The victims’ parents blamed the dengue vaccine for the deaths of their children.”

Most of the deaths were caused by internal bleeding in the heart, lungs and brain, which are symptoms of haemorrhagic dengue.

Sanofi announcement confirms facts:

Wikipedia with references: https://en.wikipedia.org/wiki/Dengvaxia_controversy

Is this an Attempt to Create a Disease Just to Sell the vaccine?

Comparison of death rates from the vaccinated and unvaccinated suggests the vaccine offers some benefit, but that is mostly based in areas and demographics where health services are poor. It is best answered by offering mobile health services in affected areas. This Australia can do, whereas maybe the Philippines can’t.

The vaccine is listed in Australia – but hasn’t been used. The Philippines incident was the last known use of the vaccine, and the victim’s court case is still underway. Given Sanofi’s admissions around the vaccine and WHO’s advisory that a serology test is needed before giving the vaccine to a person to ensure they haven’t had the disease before, I doubt this is a vaccine play.

The mRNA version of the vaccine was trialled and rejected in 2014 because it didn’t work. It’s not an attempt to feed work to Pfizer’s new mRNA factories in Australia. There are new vaccines coming through but they have the same problem – making the disease worse in people who have had it before.

Some Mosquitoes Replicate

4% of the mosquitoes in the Brazil test lived and replicated. No work appears to have been done on what happened to the offspring – were they normal or were they mutated and if so, what is the effect of that mutation?

Could a mutated progeny cause a mutation in the virus (Dengue, Zika, Yellow Fever, Malaria) which causes it to become more dangerous, infectious, etc. This is a major question to be answered – capturing and testing mosquitoes in the wild to look for mutations, and that work has not been done. It must be an element of the OGTR approval.

Mosquitoes have a life cycle of 7 – 10 days. Fall army worms (FAW) live 6 – 8 weeks, so they are present in the environment longer but not significantly so.

Cane Toad Disaster at Risk of Repeating

One Nation Senator Malcolm Roberts calls on the Prime Minister to immediately release COVID-19 modelling upon which the government bases its planned six-month hibernation of Australia.

“We can’t let this debilitating economic slow-down go on one day longer than it needs to, yet right now the government refuses to share vital information with the Australian people,” said Senator Roberts.

He added, “The data continues to show that we are passing peak COVID-19 infections, yet rather than offering people and businesses an economic recovery plan, the Prime Minister simply repeats his chorus line saying Australia could be closed for six months.”

Strong leadership making the tough and unpopular decisions does not need to remove hope from people for when lives can return to some normality.

Senator Roberts urges the Prime Minister to ensure rigorous wide testing, with strict isolation of the sick and vulnerable, allowing the healthy to return to work as soon as possible.

The Government has instead chosen to isolate the huge majority of healthy people, when data strongly suggests that with effective testing, all we need do is isolate the sick and protect the vulnerable.

“We can’t have massive swathes of the economy hibernating without any idea of the indicators that will trigger a re-start. 

Business owners and families need to make decisions around how long they can hold out and not be left in limbo.”

The Prime Minister has a duty of care to show the evidence to justify business closure for up to six months, and the indicators he will use to trigger a change in strategy.  

“No other country is promising to close its economy down for six months and healthy Australians would rather go back to work than to receive partial wage subsidies.”

Taiwan’s approach to COVID-19 should be used as a template, to primarily focus on and avoid a health crisis, and in that way avoid an economic crisis. 

Taiwan managed the virus with a clear priority on people’s health using rigorous temperature testing and hand hygiene practices, isolating those in danger and allowing the economy to keep running.

Senator Roberts added, “Taiwan with less than 260 people infected and only 5 deaths is a stunning example of how to manage the virus – putting people’s health as first priority – so that healthy people continued working and the economy barely blinked.”

Considering that about seventy-five percent of all COVID-19 cases in Australia are from people who travelled overseas or had direct contact with those travellers, the current arrangement of forced quarantine for overseas travellers should see a decline in cases within weeks. 

Once we are assured of people’s health we can end this debilitating economic slow-down and give people what they need: real hope through a plan for the next step, economic recovery.