Recently there has been some press coverage that potential running mates for Robert F. Kennedy Jr., are themselves well versed in conspiracy theories.
Kennedy, the driving force behind anti-vaccine pressure group Children’s Health Defense, which includes Children’s Health Defense Australia (recently abandoned website), is running as an independent for President of the USA. One possible running mate is Jesse Ventura who was mentioned here when the antics of Rima Laibow were reviewed. The other is Aaron Rodgers who has entertained a number of conspiracy theories including denial of the Sandy Hook shootings. Both are anti-vaxxers.
Kennedy has lobbied for years promoting the debunked link between MMR vaccines and autism. In the early days of the COVID pandemic he emerged as a vocal critic of COVID-19 vaccines. Which for a presidential contender, is understandably proving to be a problem. As measles cases rise across the US it isn’t surprising that Kennedy is not attacking vaccines on the campaign trail. In April last year Kennedy announced he would take leave of his roles as Chairman and Chief Legal Counsel of CHD, although the US site still lists him as both.
Exactly why the CHD Australian chapter URL is parked, just seven months after launching is unclear, although the Instagram page remains. What can’t be denied is Kennedy’s long history of spreading vaccine disinformation. In the early days of his campaign Kennedy talked about plans to tell NIH scientists it is time “to give infectious disease a break for about eight years”. However as his presidential campaign continues he is, according to NBC in the below clip, keeping his usual anti-vaccine message “relatively quiet”.
RFK Jr. relatively quiet on antivax message despite past ties
On Monday 22 January 2024 the unique home for all things COVID conspiracy, Café Locked Out, hosted a video titled The Launch of OpenDAEN, A free database of Adverse Events. Cutting to the chase, OpenDEAN, promoted and launched by Sharon Cousins, purported to be an easy and honest means of access to the Therapeutic Goods Administration, Database of Adverse Event Notification.
Like its namesake previously debunked here, OpenVAERS, the Australian analogue of misleading information, OpenDAEN, presents decontextualised data in a manner that seeks to create the illusion COVID-19 vaccines are inherently unsafe. That “vaccine injuries” are rampant. Again like OpenVAERS it presents as conclusive fact, reports of negative health experiences observed in, or claimed by, an individual after that individual received a COVID-19 vaccine.
Like the TGA, OpenDAEN uses the Medical Dictionary for Regulatory Activities (MedDRA), to classify adverse reactions. It provides filtering with the European Medicines Agency, Important Medical Events list and Pfizer’s analysis of post authorisation adverse events. An additional adverse reaction of “serious” has been added to OpenDAEN. Sharon Cousins is an erstwhile insurance executive, now presenting as an “independent researcher” with a penchant for criticising COVID-19 vaccines. Sharon could not share her screen and was directing suspended NSW anaesthetist Paul Oosterhuis, the third member of this Zoom presentation, around the site.
The primary data interrogation categories on the index page of openDAEN are:
Case numbers by Year, Month and Sex
Cases by COVID-19 Vaccine Type
Case Numbers by Reaction term and Age
Case by Frequency of Batch Number
Table of case number, date, vaccine manufacturer, MedDRA reactions, Death, Serious cases and the FOI request number the batch number was confirmed by.
The index page offers the following:
Above: Slideshow: OpenDAEN website
OpenDAEN is called a “free database”. Don’t be fooled. The important elements here are reports and post vaccine, combined with the fact almost all adult Australians have had two COVID-19 vaccines, as have two thirds of 5-15 year olds. Random ill health events can and do frequently occur coincidentally with vaccination. It’s also important to realise that the TGA and health authorities encourage Australians to report these events, so that over time a greater understanding of these vaccines will emerge. OpenDAEN.info provides a description on each page footer:
OpenDAEN.Info is a non-commercial and not-for-profit website for the research, study and review of the TGA (Therapeutic Goods Administration) DAEN (Database of Adverse Event Notifications) system in respect of COVID-19 vaccines. The primary source of data on OpenDAEN is the TGA DAEN system and their published FOIs (Freedom of Information).
Decontextualisation
When taken out of context and denied TGA cautionary disclaimers, the reports become hearsay temporally related to something somebody did. Nothing more. This is decontextualisation. But apparently, we are to assume causation exists. OpenDAEN claims to be able to offer up to date, conclusive data related to adverse events caused by COVID-19 immunisation. These adverse reactions are the subject of reports sent to the TGA DAEN. So, the data themselves have a recognisable source. But can absolute conclusions be made with any real confidence? In reality it takes time for clinically relevant events, specific to any vaccination to be investigated, identified and acted upon. Unless already understood and published on the TGA COVID-19 Vaccine Safety Report (2 November 2023), the quality and quantity of adverse reaction is speculation. To make matters worse, the anti-vaccination lobby has invested an exceptional amount of time spreading disinformation via social media, and one of their primary targets has been the TGA DAEN.
The anti-vaccine lobby want every report to be an absolute reality. They want the figures, diligently and honestly provided to Australia by the TGA, to be accepted without examination as conclusive, in their misguided attempt to wipe out COVID-19 immunisation. We saw this claim time and again in the court affidavits of Peter Fam, Meryl Dorey, Julian Gillespie and Katie Ashby-Koppens; reports presented as if confirmation of death and injury in huge numbers. But correlation is not causation. If you haven’t clicked the link to DAEN by now, let’s see what the TGA, but not OpenDAEN, stress about the contents.
- DAEN SPLASH SCREEN DISCLAIMER –
Okay, so it confirms what I stressed above. But most crucially, you have to tick the teeny weeny little box next to I have read and understand the above, to access the TGA data. The disclaimer can’t be missed. Only willingly ignored. The importance of what this means and the restrictions the disclaimer places ipso facto, on OpenDAEN was studiously avoided during the video on 22 January. In fairness I will note that a small header on the TGA DAEN page was visible, but also ignored. It reads; Inclusion in DAEN – medicines does not mean that the adverse event has been confirmed or that it was caused by a medicine or vaccine. Clicking it – which the presenters also studiously avoided – reveals a little more about the DAEN content. Due to size restrictions of a screenshot, I’ll pop the text in a paragraph, and include some emphasis (mine):
The DAEN – medicines allows you to search adverse event reports for medicines including vaccines received by the TGA. The TGA uses adverse event reports to identify when a safety issue may be present. The DAEN – medicines does not contain all known safety information. An assessment of the safety of a medicine or vaccine cannot be made using the DAEN – medicines alone.
Talk to a health professional before starting, stopping, or changing your prescription medicines.
Anyone can report a suspected adverse event, including members of the public, health professionals and pharmaceutical companies. We encourage reporting even when it is not clear that a medicine or vaccine is the cause. Information from these reports is published in the DAEN – medicines and reflects the observations of the person who reported the event.
People who experienced an adverse event cannot be identified. Maintaining their privacy is of critical importance to the TGA.
The DAEN – medicines is a ‘living’ database that is frequently updated. Information may change if we receive more details on an existing report or if we identify duplicate reports and combine them. Updates may also occur as part of our data quality assurance activities.
In short, the TGA DAEN database is constantly growing, contains information from any member of the public, reflects the observations of that person, provides no information about the safety or lack thereof, of vaccines and does not confirm that an adverse event was caused by a vaccine. It cannot even confirm if the event has actually occurred. I might add, dear reader, given that the anti-vaccine lobby has gone out of its way to submit to the DAEN clearly impossible and even bogus reports, one must remain extra vigilant when assessing or querying these data.
Indeed, Sharon Cousins herself relayed an abuse of the TGA DAEN system at the 8:30 mark of the video. She had queried via FOI why a reported death of a 6 year old boy was no longer available on the DAEN. Sharon noted that within her FOI report FOI 4077 (“Batch numbers of COVID-19 vaccines of reported deaths”), it was revealed the initial report was submitted as a hoax. The relevant section of the report reads:
FOI 4077 also requested information about why case number 724925 no longer appears in the DAEN. This report was rejected following review of further information for the case. The information demonstrated that the report was submitted as a hoax and as such there is no identifiable patient. The report remains in the TGA’s internal database. However, it no longer is included in the DAEN as it has been rejected because it no longer met the minimum criteria for a valid adverse event report.
Sharon Cousins
Sharon also said the TGA reply included, “Normally we wouldn’t answer this”, after insinuating she has a positive relationship with them. However, that comment is clearly not there. One appreciates Sharon sharing this information, but cannot ignore that it took an FOI query of a fatality to uncover the truth. How many other adverse or serious adverse reactions were, or will be, “rejected following review of further information for the case”. Sharon was eager to reassure viewers that OpenDAEN was not misusing the TGA website, but rather making it “more user friendly”. It will be of benefit to TGA staff Sharon opined, and she had sent the site link “to the coroners”, and to State and Territory head pathologists.
Batch Numbers
Throughout, much is made of the section allowing search of batch numbers. We learn that when it comes to accessing batch numbers, the TGA, “Doesn’t have any search engines on it, is a little bit clunky and it times out”. The TGA freely provide data in CSV format on batch release assessment of COVID-19 vaccines. One of two release pathways is taken; either based on overseas certification or based on TGA laboratory assessment. The TGA explain this in detail. So, what could be wrong with smoother navigation of COVID-19 batch numbers as a function of vaccine type, reported adverse reaction and de-identified data? Usually nothing, unless one ignores TGA advice and extrapolates to conclusion, based on other available data.
At the 50:00 minute mark Sharon directs navigation through the number of cases per batch number, highlighting batch number FP1430 – COMIRNATY, (Pfizer), in section 4. OpenDAEN has accessed the batch numbers via FOI, and that’s fine. OpenDAEN reveals inordinately more adverse reactions for male and female associated with this batch number, compared to those next to it. Sharon instructed more data access and directed navigation to the batch number table. She continued:
Look at the dates! Look at all the dates! Within 24 hours of the Pfizer being released on the younger children, the five to elevens… it was all advertised, tenth of January [2022], five to eleven year olds… within 24 hours we have reported cases. Now that for me is causal proximity.
Sharon continued on, directing suspended doctor Oosterhuis to isolate reported – not confirmed – fatalities using that batch number and age group. They isolate two boys. Zeroing in on the symptoms of one boy, Sharon reads, abdominal pain, then dismisses adverse event following immunisation as “a very bland one”, then cardiac arrest. She has Paul Oosterhuis explain eosinophilia and eosinophilia myocarditis. He assumes he is explaining the findings of both of “these boys”. In fact the data reveal clearly it is only one boy. A five year old.
The ten year old “fatality” has only Adverse Event Following Immunisation listed. The “very bland one”, dear reader. Then Sharon warns us “It’s a little bit distressing now, okay. The two boys both had the same batch number”. She gets Oosterhuis to zoom in and suggests, “So, screen print that people if you don’t believe us”. After zooming in on the case numbers Sharon has Oosterhuis zoom in on the batch numbers again, as if she hadn’t made that point enough times already.
Now, I am not a lawyer but I doubt the strength of Sharon’s “causal proximity” claim. There is another factor Sharon told us herself, that must be considered. As she points out, the roll out for Pfizer for 5-11 year olds was 10 January 2022. Thus, the first factor I would investigate would be the sheer number of children being vaccinated, at the time of release. Over 11 weeks, 76.6% of those 2.3 million children were vaccinated. 1,761,800 children had one dose. 1,552,500 (67.5%) had two doses. The vaccine for 5-11 year olds is one third the dose approved for children aged 12 years and over. Cold chain transport and storage is vital to the success of mass mRNA vaccination programmes.
Using OpenDAEN to interrogate vaccine batch numbers of adverse reports about 5-11 year olds, over the first two months of the rollout, we see virtually one result: FP1430. Yet what is more likely? Batch FP1430 is responsible for all adverse reaction reports? Or most 5-11 year olds vaccinated in the initial days, were dosed from batch FP1430? By the end of February other batch numbers begin to appear and gradually attract more reports. By late March, FP1430 is just another batch number. More so, there are over 500 unknown batch numbers for that age group. However, if you present your disinformation just right, some might believe in the deliberate harming of children:
– Facebook comment –
What do the TGA say?
There have been no deaths in children or adolescents determined to be linked to COVID-19 vaccination. More detail on these deaths is available in the safety report published on 15 December 2022… If we identify a new death likely to be related to vaccination, we will publish this information promptly, as we have for all other cases since the start of the vaccine roll-out. [Source – 2 November 2023]
Of the 14 deaths the TGA confirm are linked to vaccination, none are in the 5-11 year age group. Yet Sharon is convinced of her claim, has already convinced others and will convince more, simply because of bias. Her defence, I suspect, will be that she used FOI legislation to access reports on batch numbers and the TGA lacks the smooth batch number access and navigation of OpenDAEN. Yet Sharon made up her mind before she even started looking. In fact, Inclusion in the DAEN does not mean the event has been confirmed or determined as related to a vaccine, is utterly ignored when using OpenDAEN.
The reactions reported in January, are based on MedDRA. Seen clearly in the video, were cough, vomiting, pallor, lethargy, rash, injection site rash, syncope, cold sweat, decreased appetite, anxiety, dizziness, nausea, abdominal pain, abdominal discomfort, aggravation of existing disease, excessive sweating, hives, muscle stiffness, chest discomfort. The worst on screen were seizure, appendicitis and a seperate loss of consciousness. Searching the batch number/adverse reaction table for 5-11 year olds in my own time, revealed reports of chest pain, syncope, anaphylactic reaction, paraesthesia, ECG ST segment elevation, nystagmus, pneumonia and many others. Some reports were of one reaction and others of multiple. All reports are of conditions children experience everywhere across the globe. Establishing cause or any relationship to COVID-19 vaccines is the role of health authorities.
Elsewhere on OpenDAEN we read that:
Useful search engines, graphs and tables have been developed into a helpful user-friendly database to assist study, research, review and analysis of the Australian Government publicly available data. […] We believe in sharing this information in an open and easy-to-use format (with search engines, tables and graphs etc.) and to help make it quicker for anyone wanting to source data for their own study, research and review.
The Quack Miranda
So, the team want to share information in a fast open and easy way to help with doing your own research. It sounds almost too good to be true. The Disclaimer and Disclosure tell us:
– Source: OpenDAEN –
Okay then. It is up to the user to get further professional information to confirm if the information is “of value to you”. Accuracy of the information cannot be guaranteed which places further responsibility on the user to seek advice before relying upon it. It’s information they might get wrong and as such will not be liable “for any loss, damage, cost or expense incurred” by reason of relying on that information.
It is 2024 and world search and data systems can perform enormous and complex requests with astonishing speed and accuracy, yet when Australian governments roll out never before used experimental gene therapies to millions of citizens, Australians are left to report to an antiquated adverse event reporting system (DAENs) still with both feet in last century.
This amounts to a fundamental failure of Pharmacovigilance and the Australian People. Searching through DAENs remains a nightmare for researchers, where one cannot but question the motivations of the TGA and the Australian health departments who feed it Our Information. OpenDAEN greatly assists researchers and students, and data and IT experts desperately needed to review and criticise the current DAEN system which is not fit for purpose.
Hopefully OpenDAEN will motivate Australian governments to take the needed steps towards a national real-time, transparent, and easily accessible adverse event reporting system, for properly protecting the health of Australians and better facilitating valid Informed Consent. The antiquated DAEN system deprives and seemingly hides needed health data necessary for Australians to provide valid Informed Consent.
COVID vaccine injury class action fund raiser, Dr. Melissa McCann writes:
This is amazing and meticulous work by you and your team.
Strong reminders of OpenVAERS and how decontextualised data are used by anti-vaccine activists to mislead, were apparent during the video. Alluding to what is known as the Lazarus Report, after the name of the principle investigator, one commenter offers:
– Facebook comment –
Suggesting that TGA DAEN statistics are only “(10%?)” of “ACTUAL injuries and deaths”, is linked to a bogus belief of widespread underreporting to VAERS in the USA. I addressed this in a post challenging OpenVAERS, writing.
The figure of 1% comes from a report from Harvard Pilgrim Health Care, Inc., authored by Ross Lazarus. Data examined are from 1 December 2007 to 30 September 2010. These data include all possible adverse events. Prior evaluation of the reporting rates of various events confirms that minor events are rarely reported and more serious events routinely reported. A 2014 report on surveillance of adverse events following immunisation in NSW, Australia noted that:
Only 11% of the reported adverse events were categorised as serious.
In short, most adverse events such as a sore arm, nausea, swelling, redness, headaches, vomiting and other self correcting issues are indeed underreported, but make up the vast bulk of adverse events following immunisation. Yet since the Lazarus report, anti-vaxxers love to spread tales of widespread death and terrifying injury, then solemnly add “only 1% are ever reported”.
Paul Offit is a strong supporter of VAERS which he refers to as a “hypothesis-generating mechanism”. Reports there of intussusception approximately once per 10,000 doses led to suspension of his own RotaShield vaccine which was ultimately recalled, before returning as a safe product. In fact health authorities want parents or doctors to report minor events as soon as possible. Much can be learned about self limiting reactions, and more concerning to severe reactions can be gauged by pattern changes, properly identified and suspended under section 29D of the Therapeutic Goods Act 1989.
Perhaps the most damning page on OpenDAEN is the resources page. A curated smattering of COVID-19 vaccine pseudoscience and “vaccine injury” class actions, peppered with all the anti-COVID mandate and health advice groups, it seems designed to lead readers into a field of gaping rabbit holes. Dr. Melissa McCann’s COVID class action vaccine injuries video tops the page. The World Council for Health Spike protein detox guide is there. R.F. Kennedy Jr.’s Children’s Health Defense Australia, The Zelenko Protocol, The Australian Medical Professionals Society, many of whom we’ve met here before, World of Wellness and the National Institute of Integrative Medicine to name a few.
Conclusion
OpenDAEN is not an exciting addition to the TGA DAEN database. It is not a positive, user-friendly addition to TGA staff or to genuine researchers and academics. It is created, managed, supported and provided by and for respectively, members of the anti-vaccine community, convinced that COVID-19 vaccines are the cause of multiple health ailments and death. No professionals were available for its launch. All invitations were ignored. It has no integrity and no academic standing. No coroners or State and Territory head pathologists will care.
Like its namesake in the USA, OpenVAERS, it is designed to allow users to gather misleading collections of coincidental report material and present this as causal COVID-19 vaccine adverse reactions. To be sure, the results it produces, easy to construct as they are, will find their way onto websites, social media and court affidavits. OpenDAEN won’t enjoy the success OpenVAERS did, because now only diehards remain. During the launch of OpeanDAEN, events two years old were focused on, to craft a demonstrably bogus, yet very serious accusation against COVID-19 vaccines.
Very late on Christmas Eve 2023, Santa had just dropped me a rather special present.
I more or less knew what it was by feeling the packaging, but still fumbled hastily until it sat gleaming in my hand. There it was. A brand new COVID-19 infection.
I could hear him jingling happily into the distance, with the words “naughty” and “nice” echoing on the breeze. Then, “falsifiable hypotheses” wafted back.
Of course! I suddenly remembered a discussion years ago, soaking our blistered feet in cured reindeer urine, when he told me anything that could be falsified was inherently “naughty”. Wrongly, I thought I had properly explained things to him.
This time, I’d sort him out. “Santa, Santa. I just KNOW we’ve had this conversation before”, I yelled in his direction.
I continued.
” Making a list, and checking it twice , gonna find out who’s naughty and nice… does not a falsifiable hypothesis make. I just… I mean, I can’t even….”.
He answered with a vague reference to falsifying anti-vaxxer claims and something even more vague about my feet needing another urine soak. Next thing an apparition-like, misty glob of reindeer, a sleigh, a fat, smelly-chap, sacks of presents and boxes of Rapid Antigen Tests was in front of me. Santa folded his arms and confidently started his defence.
I responded,
“Wait! What?! Say that again. I’ve been ‘naughty’, because I revealed falsification, and therefore I can’t enjoy Christmas this year? No, no dude, you’re attributing subjective emotional qualities to the entire notion of the falsibility hypothesis. Yeah I get it – you’re saying if I hadn’t showed things were totally false that I’d have been ‘nice’, particularly because you were checking it twice. But if I may, with respect old chap, it simply doesn’t work that way.”
He laughed, pointing at me, and asked, “Why the fud not?”
I was feeling far from well but managed.
“Well because, my long-bearded, voluminous-bellied friend. The very notion that the hypothesis can be falsified, is what lends it such robust integrity in the first place. Suggesting falsifiability is ‘naughty’ and anything not shown to be false is ‘nice’, is likely a position arrived at via a sequence of logical fallacies.
He said I was making some sense but sounding very lah-de-dah. So, I went on.
“Okay, let’s agree your position is that honesty or not ‘being false’, can be labelled very simply as ‘nice’. Cool? Righto then. And that dishonesty, or being deliberately false can be labelled as ‘naughty’. So, deliberate falsehoods coming from, ooh let’s say anti-vaxxers, are ‘naughty’. In fact they are known for providing so-called data based on fabrication, and fraud. So, let’s say ‘very naughty’.
Now, that all sounds okay, but it can’t really be tested beyond the scope of opinion. It also takes unnecessary work and lends credence to fraudsters. Better then, that the theory or hypothesis is one that can be tested and logically refute the idea being questioned, particularly if the falsification can be based on empiricism (what we see or experience).”
Santa asked if empiricism was like the Black Runes-of-Empiricism that Senator Malcolm Roberts used, to make a mockery of climate change.
“Why yes, you’ve heard of him then? A total… whoa, okay… sorry, yes, yes I did see the pontoons strapped to the sleigh. Bit sloshy up North… I can grasp that. Reality and Roberts don’t get on, Santa. Not a fan are we? No Ho, eh? Ah, well… er, no we can’t do the sword thing anymore. No, no the Blood Eagle never did take on down South. Sorry. Free speech and such. Oh? Well, um, I’d prefer to say we’ve become, “civilised” but “as sturdy as walrus diarrhoea” will do for any justified criticism in this case, old chap.”
Santa mumbled on about colourful torment to Roberts for a while, many involving objects I had never heard of, then he then gradually worked his way back to chatting about falsifying arguments and hypotheses.
I jumped in.
“So, see it’s simple really. If you can devise a method to falsify an argument that someone is proposing, then it is held to a greater standard of proof because it is possible to falsify it. Even if it has never been falsified. It just means it is possible to imagine or construct an argument to falsify it.”
I was by now feeling pretty crook and thought I might try my luck at swapping my present.
“Now Santa. Maaate, buddy, bloke. I realise we’re a long way from naughty and nice but I hope this clears things up, and clafifies the obvious error of this rather unique present you’ve dropped off. I guess this is one test I’d like to have seen falsified as it were… Nudge, nudge. Any chance you can wave the magic stocking..?
What’s that? Yes, yes, I did expose a bunch of anti-vaxxer arguments as false. They were false – fabricated in fact. In fact they were all bad. Thanks for noticing – it’s quite a long way for news to travel up North. What do you mean I’m still naughty? Er, yeah, okay… sure… But dude, I don’t CARE how many times you’re making a list, and checking it twice . Didn’t you understand a single thing we just discussed?
So, I’m what now? I’m too Skeptical? So I’m naughty because I’m too Skeptical? Oh, righty-Ho-Ho! What? Well, yes I’ve had a few COVID vaccines. Oh, I see that’s what this is. But I never said they were 100% protective; that’s an anti-vax logical fallacy. Gawd, Santa! Vaccines do reduce symptoms though. What? Well, er pretty sh*t actually. I’m running a temp of 39 C. But tomorrow I won’t be.”
Incredible! Santa seemed to be warming up to Gish gallop. Time to wrap this up.
“Anyway bloke. It’s getting late. Shouldn’t you be flying toward the West by now? Time zones and all that. You’re what?! You’re not flying!? Oh?
In June this year we briefly met suspended GP registrar, William Bay, thanks to his attempt to intervene in the Australian Babies Case. He has summarised his reasons for doing so here. Suffice it to say the Australian Vaccination-risks Network were not happy, making me very happy.
Fast forward to the present, and former AVN president Meryl Dorey, who has taken to feverish promotion of cooker-conspiracy theories on Substack, revealed Saturday that the same William Bay had sent her a formal Letter of Concern. It lists numerous comments about him on her Substack site, that he believes are defamatory. Billy wants the article and every comment removed, topped off with a public apology. This is the latest event since Billy, who proudly refers to himself as the Suspended Dr. William Bay, falsely declared his High Court challenge to have the Voice referendum declared unconstitutional, was a success.
This was not the first time Billy, who often proclaims he’s doing God’s work, declared victory in stark dissonance to the facts. He is soundly refuted by AAP FactCheck here. AAP provide insight into how quickly disinformation spreads between cookers. Billy’s proclamation of victory is a great example of how the uncritical acceptance of a claim can influence belief. It also underscores the power of social media, in this regard. Billy gave a performance of confidence and credibility in a Cafe Locked Out interview, citing as proof documents that actually confirmed his failure.
During the interview he referred to a document on his website’s legal docs page headed “Application For A Constitutional Or Other Writ”. Billy directs viewers to his site then says:
I’m looking at it on my computer right now. It’s a miracle, it’s gorgeous, it’s great. It is a stamped document by Justice Jagot of the High Court itself who has declined to rule on the constitutionality of the referendum. So with this case being dismissed from further need for analysis, in legal circles as my lawyer friends will know… if jurisdiction is not proven it is invalid.
The gorgeous and great miracle was the exact document Billy had submitted for filing. The stamp added by Justice Margaret Jagot references High Court Rule 6.07.2, which deals with the management of frivolous or vexatious applications, and includes:
I direct the Registrar to refuse to issue or file this document without the leave of a Justice first had and obtained by the party seeking to issue or file it.
The upper part of the stamped application is below.
Screenshot – Billy Bay’s rejected application
Of course I am not a lawyer, and neither is Billy for that matter, but he has filed documents with the High Court before this. The Notice Of Filing cover page is part of previous documents he has lodged, displayed on his website. This includes file number, title, registry, type of document; in this case Application for constitutional or other writ, filing party and date. Think of it as confirmation that legal proceedings will take place. Plainly absent from his gorgeous miracle, it also clearly states:
Notice of filing page: Important Information
Staying in theme dear reader, I submit that the evidence before you supports the contention that the Suspended Dr. William Bay did know or should have known that his application was unsuccessful, and did know or should have known that the 2023 referendum is not unconstitutional. This conduct is not unusual for Billy who frequently offers baseless beliefs as fact.
Nonetheless, what followed was an old fashioned pile-on by various “freedom fighters” who took three days and more to decide Billy was wrong. Which interestingly, although they’d never admit it, was how long it took for AAP FactCheck to publish their rebuttal. More so, the stamped rejection of Billy’s application was available on 5 September receiving comment on social media by critics of the so-called freedom movement.
Then on 8 September, long time anti-vaxxer, AVN member, self-proclaimed “journalist” and founder of The People’s Revolution, Tristan Van Rye, better known as Triccy Triddy took to Facebook. Triccy lives in that alternate universe where nefarious global conspiracies of momentous proportion are accepted as fact. His tactics deserve proper deconstruction, but for now bear in mind he is driven by base neoconservatism. There is the ever-changing enemy to fear and there is “us”, constantly threatened by the enemy. Triccy’s a true believer and whilst he’s sowing fear, disinformation and social harm, appears genuinely convinced he is doing good.
In this video Triccy does a sound job of pointing out why Billy’s claim that the referendum is unconstitutional, can only be bogus. Chatter in the cookerverse following Billy’s announcement was reinforcing his other claim, that voting is unnecessary. Triccy had spent months sewing disinformation and anxiety about voting “Yes” and understandably couldn’t allow the chance of lost votes to go unchallenged. Other seasoned curators of disinformation felt the same way and rushed to their live streams. Senator Malcolm Roberts (who himself alleged in parliament that the ballot was unconstitutional), AVN president Aneeta Hafemeister, SovCit grifter Mike Palmer, former MMA fighter and Peacemaker founder Nick Patterson and pseudolaw obsessive Derek Balogh, all had a sudden concern for the spread of misinformation.
In the wake of Triccy’s video, Billy sent him a text message. It was reposted on Telegram:
Triccy, I hearby request and direct you to take down that FB live that you just did about me because I consider it defamatory. We have WON in the High Court. I will continue to show and explain that to the people of Australia; until it’s crystal clear for everyone I encourage you to keep an open mind to things, and in the meantime, I would appreciate it to save us all the trouble if you would remove that video please. Dr William Bay
Billy also sent a Letter of Concern to Triccy in response to said defamatory video. Triccy, in a rare moment of near jocularity, burnt it in his favourite faux lounge fire-pit. Billy however, kept up his booming confidence and applied for leave to issue or file the original application. This matter was heard on 15 September and ruled the original application an abuse of process. See p. 5, para 8:
It is not necessary to consider the question of standing, here in the context of a referendum. By r 6.07.1 leave to issue or file should be refused where the document would amount to an abuse of process. The latter term encompasses proceedings which are foredoomed to fail, as the proposed proceedings are.
Ah, foredoomed to failure, dear reader. A weighty yoke for our suspended doctor to bear. By 19 September, Billy had apologised to Triccy and withdrawn “proceedings”. Triccy was not amused, and announced an end to any further cooperation with Billy. He also took issue with a claim Billy made about employment restrictions imposed by AHPRA. We’ll get to that. First, we don’t want to forget that when Billy was gearing up to sue Triccy for defamation, someone else got their bad ass boots on. In fact there was bad assin’ and chin juttin’ aplenty from our Meryl, all with the hope of provoking Billy.
He was easy to provoke and Meryl went in hard. In a piece titled Distinguishing truth from bullsh*t 101, Meryl hit him where it hurt. It began with humour, as Australia’s most pernicious antivax liar laid out the section heading; Unity is vital – but truth is paramount. Oh, how we laughed! But next came mockery with; Billy Bay’s High Court “Victory”. Ah, the sting of those quotation marks. Then Not the first time Billy has done this, opened the way to a recounting of the failure of the Australian Babies Case. But ultimately came the totally bad ass; Will Billy Bay now come after me for telling the truth about his actions?
Having got the desired reaction, Meryl posted an article, referring to him only as “Bully” as she outlined the specifics of Billy’s letter of concern. The subheading; I don’t take well to threats, can only be described as (need I say it?) totally bad ass, and the article swiftly dispenses with any notion that Meryl is concerned. Within, she refers to a comment reply she wrote in response to Billy’s comment requesting her to “stop attacking” him. She raises the same issue Triccy Triddy had done regarding Billy’s claim on Voice of Freedom that AHPRA had prevented him from working in “any job at all”.
This is another jolly example of that area between remote possibility and reality that Billy exploits. Just as he continued to claim victory in the High Court because he had filed for leave to have his (already rejected) application accepted, there is a submission Billy refers to in the hope of convincing his followers. Simply put it is material submitted in reply from Billy to AHPRA, The Medical Board of Australia and QLD State, in the wake of his suspension. It happens to include:
So, he sought an injunction to prevent AHPRA and the Board from further enforcement of their “compliance letter” so that he can work in positions that don’t “require current registration with AHPRA as a condition of employment”. Neither AHPRA nor the Board have the power to enforce conditions outside their purview. Billy has always been free to work in areas where registration with AHPRA is not required.
Prior to this Billy had submitted an Application for Review of the findings of AHPRA and the Board. On page 7 is a request for an injunction to limit enforcement of the “compliance letter”, so that Billy could work in health care roles seperate from those of a GP Registrar.
The “compliance letter” is clear in that Billy is prohibited from working in health care. All health care, and only health care. In fact, the same document includes a November 2022 affidavit from Billy Bay which presents a clear summary of that letter on page 4, item 15:
The evidence that AHPRA ever sought to prevent Billy working “at all” doesn’t exist. Yet Billy chose to zero in on one part of a much larger, failed application to the Supreme Court. From 27:20 to 28:45 in the interview with Carl Lieberman, Billy talks about what he then thought were defamatory comments from Triccy Triddy. It was “a matter of life and death” for him because if his followers don’t trust him, donations would dry up and this was his only income. You can grab the mp3 file here or listen below. The important part is:
Billy: I even filed an application in the Supreme Court to let me work in any job at all and I lost that one…
Carl: Is that any job in health or any job at all?
Billy: At all, at all Sir… at all! It’s an outrage. It’s a disgrace and a disgust and the people of Australia need to know that, to see how unlawful this AHPRA agency is that they think they can regulate me that much. If they can do that to me they can do that to you.
Carl’s face is priceless as he can’t hide his incredulity. He asks Billy about responding to AHPRA under basic trade-law rights, but Billy had already tried “the international covenant on political and civil rights”. And so it came to pass that Triccy and Meryl called foul on this claim of Billy’s. But they were ten and fourteen days late respectively. Where did they get such bad ass information? Could it be that badder asses had earlier sought to hold Billy to account? A quick visit to Billy’s Facebook page gave me an answer of sorts. Some devious character with an obviously fake name had commented under the video, a day after it was posted:
The plot thickens! There’s also some lucky losing cast iron flying pig standing on an old copy of The Skeptic magazine and snooping around X.
@DrBillyBay Can you support your claim of being prevented by AHPRA to work in “any job at all” please? You’re suspended, and AHPRA suspension outcomes are clearly stated on their website. I’m worried you might inadvertently reinforce Triccy’s claim you “spruik misinformation”.
Humour aside, there are serious elements to consider in the wake of Billy’s ultimately harmless threats against seasoned con-artists. It’s breath-taking to witness Meryl Dorey, architect of the 2016 No Jab No Pay High Court scam, levelling accusations of donation fraud against him. NSW Fair Trading found the AVN guilty of breaching the Charitable Fundraising Act 1991, yet decided not to press charges. As for the money Dorey admitted to hoarding, furious AVN donors had to swallow the loss of their $160,000. Yet she recently wrote about Billy:
So Bully is gaining money from our suffering community under false pretences and I exposed that along with several other long-time supporters of health freedom and informed choice.
Meryl exposed nothing others hadn’t revealed two weeks before. Her own false pretences ensured a career sabotaging public health initiatives and scamming donors. Prior to the formation of the unfunded volunteer group, Stop The AVN, her unceasing schemes ran unchecked. COVID was a double-edged sword; bringing more followers to anti-vaccine conspiracies, but ensuring the increasing irrelevance of the Cult of Meryl. Even the AVN court cases failed. The frustration seeps through in this stand-over advice she offered Billy.
Better than you have tried to censor me for nearly 3 decades and they have not been successful. Perhaps it’s time for you to do some deep soul searching Bully and try to work out why you are actually involved with this issue. Because as far as I can see, it doesn’t appear that caring for our community and the lives of the children and adults therein is your main motivator.
Triccy was far more diplomatic in his criticism, stressing that he meant Billy “no harm”. Unlike Dorey, Triccy appears genuinely focused on change rather than profit and ego. That said, his belief that “we are experiencing World War III, which will be known in the future as The War Against the People”, is based on harmful conspiracy theories of shadow governments. Whilst a key aspect of his rhetoric is that “people will forget their differences”, he is quite skilled at ensuring division between what he wants and what most of us identify as progressive thought.
Billy himself has spent over a year filing for court cases, circling social media and attending protests, after he publicly sabotaged his medical career at an AMA conference in July 2022. Like these other two judging him, he spends a great deal of time spreading disinformation to suit his own bizarre ideology. He also scoops up donations from gullible supporters drawn to conspiracies.
Ultimately, trouble in cooker paradise is nothing short of great news. Belief in conspiracy theories and suspicion of vaccines have both increased post COVID. Researchers are refining their understanding of the factors behind distrust of health authorities. Yet the role social media played in warping uncritical minds during lockdown, has today been replaced by quick-changing narratives adapted to suit. Attacking the Voice referendum is a case in point.
For a long time yet, anything that reflects positive social change will be seen by these players as the latest phase of dark conspiracies. I for one wish them all the infighting and trouble they can muster, and may they tear their angry little worlds asunder.
In a previous post we looked at the unsuccessful attempt of the Australian Vaccination-risks Network to convince the Federal Court of Australia it had legal standing to challenge the COVID-19 vaccine rollout.
They sought a writ of Mandamus to overturn provisional registration of mRNA and AstraZeneca COVID-19 vaccines, and a Judicial Review to overturn provisional approval of Pfizer’s vaccine for 5 to 11 year olds.
The evidence was intended to demonstrate lack of safety and efficacy of the vaccines. The plaintiffs contended the vaccines should not have been provisionally approved or registered. Indeed, that they should have been cancelled or suspended because of an imminent risk of death or serious injury. Thus, the Secretary of the Department of Health had erred in his duty to “cause to be maintained” the Australian Register of Therapeutic Goods.
However the evidence and legal arguments were never heard in court. The AVN had no “special interest”, and thus standing. On 8 August 2022 their appeal against this finding was found to be incompetent. A couple of months later, lengthy correspondence went out to all “donors and potential donors”. Headed AVN Legal Actions and Strategiesthe document opined on the issue of standing:
The way that the current case law is being applied by the Federal Court is essentially to say that nobody has sufficient standing to challenge these therapeutic ‘goods’, nor indeed the Secretary of Health.
The Babies Case
The AVN had decided to take “an alternative course of action”. One that had been researched and prepared by retired barrister Julian Gillespie and solicitors Peter Fam of Maat’s Method and Katie Ashby-Koppens of PJ O’Brien and Associates. In view of the AVN’s recent outcome it was deemed wiser to approach the High Court with “The Australian Babies Case” (AuBC), and seek to “halt the provisional approval of the Moderna jab from being injected into our precious 6 month old to 5 year old infants”. The AVN would “change course” and become a co-applicant with five others.
The other applicants were:
Associate Professor Peter Parry
Dr. Julian Fidge
Dr. Shoba Iyer
Dr. Astria Lefringhausen
Mark Neugebauer
The first three applicants above are active members of the Australian Medical Professionals’ Society (AMPS), a Red Union group that formed with the specific aim of challenging the rollout of COVID-19 vaccines, fighting COVID-19 mandates and promoting controversial treatments such as Ivermectin and hydroxychloroquine. Parry is also the lead applicant challenging the State of QLD over health professional’s vaccine requirements and a key member of Doctors Against Mandates. Three months before the AuBC strategy was outlined in this document, the AVN published the full AMPS Medico-Legal Summit on its website.
The breakdown of speakers at the summit includes AVN legal consultant and primary researcher behind the AuBC Julian Gillespie, primary plaintiff Prof. Peter Parry, Senator Malcolm Roberts and Senator Gerard Rennick. We will meet Senator Rennick again, later in this post. In lobbying the SA Minister for Child Protection, plaintiff Mark Neugebauer cites AMPS correspondence from Dr. Christopher Neil, another speaker at the summit. Gillespie and Ashby-Koppens appear on AMPS Discussions From The Frontlineupdating legal activity |2|.
The document went on to outline the strategy behind this new approach:
In The Australian Babies Case, the legal strategy is to present five applicants before the High Court of Australia, and show the Court how each applicant is affected by the actions and inactions of the Secretary of Health, with respect to the Covid-19 drugs made available to babies and young children, and the rest of the Australian community in circumstances where, prima facie, preventable deaths, illnesses, and injuries in extraordinary numbers are associated with their use; and where most of the population does not need them; however despite the expertise and evidence possessed by the various five applicants, the current law on standing in Australia is deficient, and will not recognise any of the applicants as proper parties for suing the Secretary of Health.
Australian Babies Case legal research team
Julian GillespiePeter FamKatie Ashby-Koppens
It further outlined that the Babies Case would be seeking to have the High Court “fix the law on standing” such that the applicants would be accepted as having “special interest”. Namely, “the preservation of human life from preventable death, illness or injury”. It was claimed, albeit without evidence, these preventable outcomes were being seen now, due to “COVID-19 drugs” and that this constituted an “iatrogenic catastrophe”. That is to say, a catastrophe caused by the diagnosis and treatment of a condition.
Mark Robinson SC who represented the AVN in the initial failed case, confirmed this new approach was viable and advised that the High Court “has indicated that it wishes to revisit the law of standing in Australia”. They would be seeking:
A new Special Interest regarding the preservation of human life.
If successful, a court-granted injunction to halt the provisional approval of COVID-19 vaccines to babies 6 months to 5 years and children 6 to 11 years of age.
If the High court recognises this new special interest for standing, that the High or Federal Court immediately hear the Judicial Review cases for both childhood age groups and the original Mandamus case for mRNA and AstraZeneca vaccines.
If successful, the AVN expected to be able to proceed with their initial cases. As “a matter of convenience” the AVN would seek to take over the running of the Judicial Review case that involved children 6 months to 5 years (the AuBC). The AVN note that they feel joining the case “operates as a de facto appeal” from the 8 August 2022 Federal Court appeal decision.
The application was filed with the High Court on 20 December 2022. The day before, a media release was published by AVN president Meryl Dorey. It provided some initial insight into the legal tactics to be employed in this quest for a new category of standing. Resurrected anti-vaccine themes from the initial Federal Court case peppered a quote attributed to Julian Gillespie (bold mine):
The High Court of Australia is now being called upon to protect our youngest from participating in an acknowledged and ongoing Phase III clinical trial, to receive experimental drugs involving unprecedented levels of reported adverse events, including deaths… for a virus also acknowledged to pose no threat to our Babies and Toddlers…
At this point it’s worth noting that, in public discourse, the Australian Babies Case legal team studiously avoid discussing the 3 August 2022 ATAGI recommendations for this age group. Namely:
ATAGI recommends COVID-19 vaccination for children aged 6 months to <5 years with severe immunocompromise, disability, and those who have complex and/or multiple health conditions which increase the risk of severe COVID-19.
More so, the legal team make much of the fact severe cases of COVID-19 are not common in this age group, and thus provisional approval of Spikevax suggests nefarious, and not clinical, motivation. Yet ATAGI clearly state:
ATAGI’s guidance takes into account:
The very low risk of severe COVID-19 (e.g. hospitalisation due to COVID-19) in healthy children aged 6 months to <5 years. This age group is one of the least likely age groups to require hospitalisation due to COVID-19. Among the small number who are hospitalised or who die due to COVID-19, underlying medical conditions or immunocompromise are frequently present. […]
The plaintiffs alleged Spikevax is a “genetically modified organism”. As such, Brendan Murphy, Secretary of the Department of Health had failed to comply with yet another section of the Therapeutic Goods Act 1989 (TG Act). As expected a writ of certiorari would be sought to quash provisional approval of Moderna’s Spikevax vaccine for children 6 months to 5 years. A writ of mandamus (where the court orders an official) was originally sought to have the application to approve Spikevax, reviewed under law. It was ultimately abandoned. For more specific insight we must turn to the application.
Legal Arguments
The plaintiff’s argument had two grounds, and a section headed Reasons Why Remittal Not Appropriate. Those reasons argued that the case should be heard by the High Court because that court had the power to accept the need for, and then admit for hearing, a new category of standing. Thus the High Court should not remit (send back) the case to the Federal Court. They contended that the principles for standing should be more liberal when a person can establish the subject matter involves life threatening or debilitating medical conditions and they seek to preserve human life. In short:
Where the fabric of human life might be compromised or adversely impacted, interested and involved members of the public should have a right of standing in such circumstances.
Whilst I don’t accept the argument for a new category of standing in this manner, I do agree that the law is frequently lacking. In fact, it’s about here I suspect a number of Australian vaccine proponents, Skeptics and opponents of the anti-vaccination lobby may feel a dash of Deja Vu.
In 2010, following complaints from the public about misleading AVN advice, the NSW Health Care Complaints Commission published a “damning report”. The AVN successfully appealed the ruling because whilst the HCCC had jurisdiction, the complaints lacked evidence that anyone had acted on AVN advice. The appeal outcome led to the Health Legislation Amendment Bill 2013 in NSW Parliament, allowing the HCCC to act on the likelihood of harm. A follow up inquiry was launched and a second, more in depth Public Warning against the AVN was published in 2014.
Let’s return to the present. The plaintiffs also argue that there are “important questions about the lawfulness of Commonwealth officials to make provisional determinations” that impact wellbeing. They allege there is no real jurisprudence about this in the context of the TG Act. Yet in reality, the standard of evidence required to make these determinations is high and the TG Act is comprehensively designed to minimise risk. Indeed failure to make provisional determinations may risk the wellbeing of the nation.
Ground One of the plaintiff’s argument again takes us to the TG Act. Specifically Section 22D(1), which provides that the Secretary must decide to make or refuse to make a determination, when a valid application has been made. In this case the application was for Spikevax (elasomeran), which the Secretary provisionally approved for children 6 months to 5 years, on 19 July 2022. The plaintiffs argue that s 22D(1) “is subject to an implied restraint”, that the decision will be legally reasonable. They submitted:
Legal reasonableness, or an absence of legal unreasonableness, is an essential element in the lawfulness of decision-making.
Referring to “the decision” to provisionally approve Spikevax for the ages under discussion, the application is dismissive of evidence used. It cites the TGA document Australian Public Assessment Report for Spikevax, 19 July 2022. Yet the Submission overview and risk/benefit assessment, accommodates no less than half of the 31 pages. This was updated on 8 November 2022; 42 days prior to filing of the plaintiff’s application, and contains 8 subsections covering 55 of the document’s 69 pages. Subsections include, but are not limited to, Quality, Risk management plan, Risk-benefit analysis, Additional clinical data and Second risk-benefit analysis.
The plaintiffs further argued that the Secretary’s decision that Regulation 10L(1)(a) of the Therapeutic Goods Regulations 1990 (TG Regs) was met, is legally unreasonable. That particular regulation states under Provisional Determinations:
(1) For the purposes of subsection 22D(2) of the Act, the criteria are all of the following:
(a) an indication of the medicine is the treatment, prevention or diagnosis of a life-threatening or seriously debilitating condition;
In other words it was legally unreasonable to accept that the vaccine ever contributed to the prevention of serious illness brought on by COVID-19 in children 6 months to 5 years. This argument is a repeat of the AVN tactic seeking Judicial Review in the initial Federal Court Children Decision case, where they also targeted s 22D of the Act.
This was cited because the AVN also sought an order quashing any determination made by the Secretary pursuant to section 22D, that an indication of the vaccine:
“[W]as the treatment, prevention or diagnosis of a life-threatening or seriously debilitating condition for children aged 5 to 11 years of age.”
The plaintiffs continue to argue their case for “legal unreasonable decision-making” by again turning to the TG Act. They argue the Secretary has failed to satisfy requirements in s 25(1)(d)(i). Section 25 deals with evaluation of therapeutic goods, and the cited subsection provides:
(d) for an application for provisional registration of a medicine:
(i) whether, based on preliminary clinical data, the safety and efficacy of the medicine for the purposes for which it is to be used have been satisfactorily established.
Put more simply, the plaintiffs contend that when the Secretary was evaluating Spikevax, the data he used did not “satisfactorily establish” its safety and efficacy. This, they allege, amounts to legal unreasonable decision-making.
Genetically Modified Organism
Ground two of the plaintiff’s argument stated that the Secretary failed to comply with s 30C(2) of the TG Act. Section 30C provides for Consultation with the Gene Technology Regulator (OGTR). The cited subsection reads:
It appears that there has been non-compliance with a statutory condition in the TG Act. […] The plaintiffs contend that non-compliance with the statutory obligation mandated by s 30C(2) leads to the invalidity of the registration decision that followed.
Could it be that the Secretary did not have to notify the OGTR? As fate would have it we are assisted here by questions from Senator Gerard Rennick. On 16 February 2023 during a Community Affairs Legislation Committee Estimates hearing, Rennick questioned our current gene technology regulator, Dr. Raj Bhula, about s 30C of the TG Act, asking if the Secretary had written to the OGTR in regards to mRNA vaccines.
You can read the full exchange on Rennick’s website, or watch the video of it below. However, I’ll cut to the responses that matter with respect to the AuBC. Does the Secretary have to notify the OGTR?
Dr Bhula : No, because the mRNA vaccines are not required to be regulated through the OGTR.
Senator RENNICK: Did they write to you and actually ask you that question?
Dr Bhula : No, because they’re not required to be regulated through the OGTR.
Senator RENNICK: But how would they know, because you’re the expert? And, by the way, gene technology involves both replication and transcription.
Dr Bhula : Yes.
Senator RENNICK: Which is what the mRNA vaccine does.
Dr Bhula : But the mRNA COVID-19 vaccines did not involve any step of genetic modification—
Senator RENNICK: They produce proteins.
Dr Bhula : or a GMO—
CHAIR: Senator Rennick, would you allow Dr Bhula to finish her answers.
Dr Bhula : which meant that that didn’t require regulatory oversight by the OGTR.
An unambiguous answer. Interestingly, this wasn’t published on Rennick’s website at the time of the exchange. It was published 20 March 2023, which was four days after the High Court decided not to hear the AuBC. A coincidence? Unlikely, dear reader. As mentioned above, Senator Rennick, the AuBC plaintiffs, key legal researcher for the case and the AMPS are linked by their COVID-19 ideology and related lobbyist activity.
Gerard Rennick questions Dr. Raj Bhula, Office of Gene Technology Regulator
For the purposes of the AuBC affidavit, I acknowledge the confusion surrounding mRNA vaccines and GM technology. The AstraZeneca COVID-19 vaccine using a genetically modified chimpanzee adenovirus, is a clear example of GM technology. The OGTR Risk Assessment and Risk Management Plan for that vaccine is here. Years earlier the OGTR published a similar plan for a GM Live Attenuated Influenza Vaccine. The TGA acknowledges both examples as GMO medicines.
Technology applied to extract, multiply and distill the mRNA used in vaccines to instruct our cells to produce the spike protein of SARS-CoV-2 is different to the genetic modification of an adenovirus or a live influenza virus. Dr. Bhula describes it as not involving “any step of genetic modification or a GMO”.
Nonetheless, the Australian National Gene Technology Scheme lists mRNA COVID-19 vaccines, including Spikevax, as GMOs used as medicines. An Open Access Government article states, “mRNA and viral vector vaccines are derived using techniques of genetic modification (GM)”. The Alliance For Science distinguishes between the two. “This one really is genetically engineered”, it says of the adenovirus vaccine, after discussing mRNA vaccines.
We must accept Dr. Bhula’s position that mRNA vaccines are not required to be regulated through the OGTR. For the sake of the AuBC affidavit, s 30C(2) of the TG Act does not then apply, and the provisional registration of the mRNA vaccine Spikevax, is valid.
Case Remitted to Federal Court
The plaintiffs did not appear before the High Court. On 16 March 2023, Justice Stephen Gageler remitted the case to the Federal Court of NSW, as per the following order. A summary page is below.
No weight was given to the legal arguments raised, although it was noted there were “supporting affidavits totalling more than 2,000 pages”. What’s important is Justice Gageler’s observation that the Secretary had submitted that the proceedings should be remitted to the Federal Court which would have jurisdiction, under Section 39B(1) or (1A)(c) of the Judiciary Act. That section follows parliamentary action in 1997, to transform the Federal Court into one with more general jurisdiction (see p.9), including jurisdiction over any matter, “arising under any laws made by the Parliament [excluding criminal implications]”.
Justice Gageler observed:
I am satisfied that this matter is one “arising under” the TG Act for purposes of s 39B(1A)(c) of the Judiciary Act, and that the Federal Court has jurisdiction over its subject-matter and the parties on that basis.
Justice Gageler reflected on the plaintiff’s claim that the High Court was the only appropriate Court to decide on a new category of standing due to “special interest” arising when “the fabric of human life might be compromised or adversely impacted”. He stressed that the power to remit is discretionary “to be exercised after due consideration of all the circumstances of the case”. Justice Gageler cited another case as instructive, in that the power of the remitter is designed to ensure the High Court is not diverted from its principle functions by matters that “could properly be brought in an Australian trial court”. After offering his assessment of the significant scale of the case, Gageler concludes:
Having regard to these considerations, significant case management and fact finding are likely to be required to conduct a hearing of the kind contemplated by the application. Undertaking that task would unduly divert the Court from its principal functions.
“We are Discontinuing the Australian Babies Case”
The plaintiffs did not return to the Federal Court. On 12 April 2023, instructing solicitor Peter Fam of Maat’s Method published an article, and a longer explanatory video, in which he labels the vaccines “a poison”. In view of their 2022 failures with the Federal Court, further chances were poor. Even if successful, there may be repeated appeals lasting over a year. They did not have the money or time. “People are being injured and dying every day”, from COVID-19 vaccines, Fam said without evidence.
Fam added; “Too much money has been usedon facetious exploits and actions… things that haven’t been thought out in terms of strategy… people aren’t working together… doing things that are contradictory to each other… I have to take some responsibility… we lost the AVN case… a lot of money had been donated to that case”.
However:
All is not lost. This is a pivot; not a retreat, and there are other matters we have been working on simultaneously with this one, with better prospects of success than this case would have in the Federal Court. Those efforts will be formally launched within weeks, and you will hear more about them soon.
Dr. William Bay
A final mention must go to suspended GP registrar, William Bay. Bay has become a favourite amongst “cooker” watchers since he chose an AMA conference to film himself yelling anti-vaccine conspiracies, and call Chief Medical Officer, Paul Kelly “a liar”. A client of Peter Fam, Bay was asked to join the AuBC as a plaintiff. Shortly after he wanted to swap his position as plaintiff with the parent of a vaccine-injured child, believing this gave the team a greater chance at success. Fam and Gillespie disagreed. Nor could such a client be found.
Later, he filed for leave to intervene in the case as he objected to the nature of the special interest standing. He argued that if granted, the existence of standing granted via special interest in “the preservation of human life from preventable death, illness or injury”, could be used to justify COVID-19 vaccination for children. You can read Julian Gillespie’s “urgent” letter to supporters on this matter here.
Understandably, Bay further argues that such special interest standing may then be used to interfere in the application of medicine and the doctor-patient relationship in areas unrelated to COVID-19 vaccination (see video 56:45). Gillespie argues, quite rightly, that the request for standing applies to administrative and not private law. What Gillespie omits though, is any appreciation of how administrative changes impact private citizens.
Conclusion
The Australian Babies Case sought to convince the High Court to accept that medically qualified applicants had “special interest” preventing “death, illness or injury”, in babies and small children. Success would lead to a new category of standing, and this would permit the AVN to return to the Federal Court to pursue this case and its original 2022 Federal Court case, AVN v Secretary, Dept. Health.
Case evidence involved a revamping of prior legal tactics. The Therapeutic Goods Act was exploited by the plaintiffs to demonstrate regulatory failures on the part of the Secretary of the Department of Health. These failures, they again argue, justify overturning the registration or approval of COVID-19 vaccines. Driving this action was a suite of fallacious claims and misrepresented statistics.
The plaintiffs are members of and/or closely associated with the AMPS, a well organised union of medical and allied health professionals, working actively to undermine confidence in COVID-19 vaccines. Members of the legal team in this case are strident anti-vaccine activists, closely associated with AMPS, and outspoken anti-vaccine politicians.
Despite the label of “Babies Case”, this was all about giving the AVN a second chance for legal standing to have their case demanding an end to all COVID vaccines, heard in the Federal Court. Had standing been granted via a special interest as described above, it could be used to target all vaccines and help Meryl Dorey advance her life-long claim that “no vaccine is safe”.
According to the instructing solicitor of the AVN, further action should be expected soon.
Making a list, 
and checking it twice 
, gonna find out 
Losing In The Lucky Country 