URGENT independent overhaul of government power NEEDED

31st Aug, 2021
The prolonged 'imprisonment' of many Australians until most of the nation is vaccinated is the most irresponsible action by government so far. On par is the recent decision to vaccinate adolescents. Let us explain the reasons why.
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So let's dig a little deeper.
 
1. How reliable is the Therapeutic Goods Administration (TGA)?  
  • The Pfizer and AstraZeneca vaccines to this point are ONLY 'provisionally' approved by the TGA [1] and have never been fully approved as our government falsely declares [2], which is the basis of coercion.
  • The Pfizer [3] and Astra Zeneca [4] vaccines are still undergoing trials, which are thus incomplete, and therefore it is too early to determine the short to long-term adverse health consequences [5]. However, these may never be determined because trial subjects given a placebo are offered vaccination well before completion of the trials [6].
  • According to TGA reports, ALL of the clinical trials used for their assessments were conducted by vaccine manufacturers and developers and NONE were independent [7], [8], including those informing the recent 'provisional' approval for use on adolescents (conducted by Pfizer) [9]. This same report refers to the use of the Pfizer vaccine on children aged from six months to 12 years, in a clinical trial conducted by BioNTech SE / Pfizer [6].
  • Monitoring and reporting of adverse events is inadequate [10]. For example, a very small fraction of the total vaccinations is being monitored [11], and only for a short time – maximum 42 days [12]. According to US cardiologist, Prof. Peter McCullough, three to six months after their vaccination, he sees patients with newly developed chronic diseases – neurodegenerative or cardiac disease [13].
2. Can we trust The Doherty Institute?
 
The government uses The Peter Doherty Institute modelling to inform their response to COVID-19 [14]. Recently Prof. Jodie McVernon also used their modelling to inform her recommendation to vaccinate adolescents [15].   
 
The Peter Doherty Institute is also in collaboration with the Vaccine and Immunisation Research Group (VIRGo) / Murdoch Children's Research Institute [16], which has received funding from vaccine manufacturers GSK, Janssen, Merck, Novavax, Sanofi and Sequiris [16].
 
Prof. Jodie McVernon, spokesperson and researcher for The Peter Doherty Institute for Infection and Immunity, COVID-19 Research [17] also has conflicts of interest with Pfizer and other vaccine manufacturers [18].
3. Can we trust advice from conflicted medical officers?
 
Government uses incentives for doctors [19] to vaccinate, promote and advertise vaccination and restrictions BUT penalises doctors who disagree with government policy or actions [20]. Government should seek advice from a broad range of relevant opinion, such as doctors from the COVID Medical Network who are often critical of government measures and recommendations [21].
4. How well do COVID vaccines work?
 
We are in a country with very low COVID exposure and COVID illness and only a short history of COVID vaccine use. So the experience of COVID and COVID vaccination in other countries may help to answer that question.  For example:
 
ISRAEL
Has a high vaccination rate and exposure. “The Health Ministry had reported earlier this month that the Pfizer vaccine was only around 64% effective at stopping coronavirus infection with the Delta variant, compared to 95% against the original strain – and perhaps even less.” [22]. Data produced by the Israel Ministry of Health is consistent with poor efficacy [23].
 
UNITED KINGDOM
As they call for an end to mass testing, scientists warn that the Delta variant has wrecked hopes of vaccination producing herd immunity and that “there is no way of stopping SARS-CoV-2 spreading through the entire population”. [24]
 
USA
It may be that in the short-term COVID -19 occurs less often in fully vaccinated people, BUT on 27th July 2021, the CDC stated (Note: CDC owns patents on some vaccines [25]), “Fully vaccinated people with Delta variant breakthrough infections can spread the virus to others” and “the Delta variant seems to produce the same high amount of virus in both unvaccinated and fully vaccinated people… [but] the amount of virus produced by Delta breakthrough infections in fully vaccinated people also goes down faster than in unvaccinated people" [26]. Another study indicated similar conclusions [27].
 
A clear example from a recent outbreak in Massachusetts showed that among five COVID-19 patients who were hospitalised, four were fully vaccinated [27].
 
Could it be that those who cannot respond well to the virus also cannot respond well to the vaccine? [28]   
 
FRANCE
French Nobel Prize winner, Prof. Luc Montagnier states, “Mass vaccinations are a scientific error as well as a medical error. It is an unacceptable mistake. The history books will show that, because it is the vaccination that is creating the variants.” [29] In other words, “Vaccination along with other impediments (social distancing, masks) to virus transmission may facilitate the rise to dominance of new and more virulent or transmissible variants.” [30]  
5. Too many unknowns to justify the drastic measures?
 
The long-term side effects are unknown.
 
Prof. Montagnier states, “We’re in unknown territory and proclaim mandatory vaccines for everyone. It’s insanity. It’s vaccination insanity that I absolutely condemn. I want to say as well, that I never, never said that everyone will die from the vaccine, but that a certain amount of people who take the vaccine will suffer from it. That’s impermissible.” [31]
 
Once the elderly and others with co-morbidities are vaccinated, there is little reason to vaccinate the remaining healthy young and adults. This is because vaccines are harmful [32] and the remaining population is at low risk of severe disease [33], that is, they are at high risk of asymptomatic or mild infection and consequent acquired natural immunity.
6. What about natural immunity?
 
In Israel, naturally induced immunity from infection (with or without symptoms) is more comprehensive and enduring than vaccination induced immunity [34].
 
As stated by the very pro-vaccination Prof. Robert Booy: “This resilience of healthy children begs the question of whether they need to be routinely vaccinated against COVID-19.” [35]
 
Vaccine herd immunity is impossible because:
  • vaccination does not stop transmission, as seen with the Delta outbreak in Singapore [36] and Iceland [37] and other countries (as mentioned above).
  • a recent study in Vietnam examined Delta breakthrough transmissions between vaccinated people [38].
  • vaccination MAY provide only a short-term and precarious immunity [28].
7. Conclusion
 
Why impose draconian measures that impact ALL Australians financially, physically and mentally, and destroy businesses, not only for the short term, but also for the long term?
 
To vaccinate healthy people to protect the vulnerable is unreasonable when the vaccinated can be infected and infect.
 
Given that the greatest risk is to those with co-morbidities, most of which have been preventable but endemic and increasing for more than 50 years, why has government not used draconian measures to prevent those illnesses; not spent hundreds of billions on preventative health education and 'incentivisation' nor signalled an intention to do so? Not even during 'COVID times' – when advertisements promoting junk food and misuse of medications have continued to flourish, making Australians more vulnerable to infections of all kinds. THAT is the great, irresponsible selfishness [39]. It is often co-morbidities that turn SARS-CoV-2 infection into COVID-19 – the illness. 
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BETTER SOLUTION? As vaccination does not stop transmission of the virus and the healthy are not at risk of developing severe illness, why not allow natural immunity amongst the healthy? This would, in contrast to vaccination induced immunity, have the benefit of a longer and more comprehensive immunity that better protects the vulnerable from viral transmission.
 
Dr John Gerrard, an infectious diseases physician from the Gold Coast University Hospital, has stated, “But what we can at least do with the vaccine – and this is critical – is protect people from getting serious illness. If the virus transmits like a normal respiratory virus and doesn’t cause serious illness, then that’s not a problem. In some respects, it might be a good thing because mild COVID infections might induce more immunity in the population.” [40]. However that effect (induction of more immunity in the population), would be even greater as a result of transmission from the unvaccinated.  When infected, they too are likely to experience mild illness or remain asymptomatic.
 
So, with the majority of the elderly and those with co-morbidities vaccinated, and with a claimed good chance of thus preventing severe illness in those vulnerable groups, it would only be fair and just that healthy members of the population could choose their own protection from severe disease, either via vaccination or via their natural immunity, WITHOUT vilification, coercion or restrictions, that is, without the risk of triggering immune compromising stress and fear [41].
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And finally, we demand an URGENT independent investigation into government overreach, conflicts of interest and unnecessary, counterproductive fear-mongering, as well as a moratorium or injunction on any further jabs until the investigation is completed.
REFERENCES:
[1] TGA COVID vaccines “provisionally approved” https://www.tga.gov.au/covid-19-vaccine-provisional-registrations
[3] ASTRAZENECA
     ISRCTN89951424: Expected to run for: October 2021
     NCT04516746: Estimated Study completion date: February 14, 2023
     NCT04540393: Estimated Study completion date: May 11, 2021
[4] PFIZER
     NCT04368728: Estimated study completion date: May 2, 2023
"Clinical trials provide information about many of the possible adverse events associated with a therapeutic good, but do not detect all possible adverse events because they:
usually do not continue for long enough to detect adverse events that take a long time to develop
do not include enough patients to detect adverse events that occur rarely
do not include all of the different types of people who might eventually use the product and who might be more susceptible to some adverse events, such as older people, children, pregnant women or people with other medical conditions."
[6] Clinical Trial no. C4591001 referred to in AUSPAR report, uses 6 months to 12 years of age, provided by Pfizer vaccine developer and manufacturer, due for completion September 23, 2023 https://clinicaltrials.gov/ct2/show/NCT04816643
[7] AstraZeneca / Oxford: ChAdOx1-S Feb 2021 (9 clinical trials) https://www.tga.gov.au/auspar/auspar-chadox1-s
     - 5 were conducted by the vaccine’s developer; the University of Oxford
     - 3 were conducted by AstraZeneca
     - 1 was conducted by vaccine manufacturer Serum Institute of India/Indian Council of Medical Research
[8] Pfizer / BioNTech: Comirnaty BNT162b2 (mRNA) Jan 2021 (2 clinical trials) https://www.tga.gov.au/auspar/auspar-bnt162b2-mrna-comirnaty
     - 2 were conducted by vaccine developer BioNTech
[9] Pfizer / BioNTech: Comirnaty BNT162b2 (mRNA) Jul 2021 https://www.tga.gov.au/sites/default/files/auspar-bnt162b2-mrna-210722.pdf
The sponsor also submitted the six month safety data following the second dose as part of the post approval commitment to the original provisional approval for individual older than 16 years of age.
[10] Our previous press release dated 28th Jun 2021, “An IMOP Investigation into claims that vaccines undergo stringent assessments by TGA”, provides evidence the lack of adverse event reporting: https://imoparty.com/TGA-assessment-investigation
[12] AusVaxSafety 42 final day followup: https://www.ausvaxsafety.org.au/covid-19-vaccine-safety-surveillance/covid-19-vaccine-safety-surveillance-faq Click on “How does AusVaxSafety monitor the safety of COVID-19 vaccines?”
[13] Dr. Peter McCullough, cardiologist, epidemiologist and full professor of medicine at Texas A&M College of Medicine in Dallas with a master's degree in public health:
“I've seen it in my clinic and they seem to be emerging three, four or five, six months later after vaccination … So I'm getting increasingly alarmed here that this is not just a simple one- or two-day problem. And so there's great concern, particularly in younger kids that over a course of three or six or nine months, they'll end up with heart failure or cardiac death.
… What I see is, potentially from these signals, not mass death, but just a large number of Americans and people around the world with a new chronic disease of some sort of neurodegenerative disease or cardiac disease. The patients that I'm aware of, these problems seem to be quite disabling.”
[16] Murdoch Children’s Research Institute Funding & collaboration through VIRGo: https://www.mcri.edu.au/research/themes/infection-and-immunity/vaccine-and-immunisation-research-group-virgo  Click on "Funding & Collaborations" for funding; andhttps://imoparty.com/COI-References Ref 71, for screenshots
[18] Jodie McVernon – detailed COI can be found https://imoparty.com/Press-Release-COVID-19-vaccines-set-for-Australia
     - Director of Influenza Specialist Group https://www.health.gov.au/sites/default/files/atagi-conflict-of-interest-disclosures.pdf, which received funding from vaccine manufacturers Abbott, GSK, Seqirus, Pfizer, Roche and Sanofi http://www.isg.org.au/index.php/about/sponsorship-and-support/
     - Investigator on clinical trials funded by vaccine manufacturers GlaxoSmithKline, bioCSL, Novartis and Pfizer https://www.health.gov.au/sites/default/files/atagi-conflict-of-interest-disclosures.pdf.
     - Member of Asia-Pacific Alliance for the Control of Influenza (APACI) https://www.apaci.asia/about-apaci/membership, which has received funds from vaccine manufacturers IFPMA, Roche and Seqirus/CSL https://www.apaci.asia/about-apaci/support-grants
     - Member of ATAGI's COVID-19 Working Group https://www.health.gov.au/committees-and-groups/australian-technical-advisory-group-on-immunisation-atagi-covid-19-working-group#atagi-covid19-working-group-members which provides advice to the Minister for Health on the immunisation program for COVID-19 vaccines as they become available in Australia.
[20] AHPRA Position Statement - Registered health practitioners and students and COVID-19 vaccination: https://www.ahpra.gov.au/documents/default.aspx?record=WD21/30751&dbid=AP&chksum=zrOQ56xJaaLbasNxLDyqMA%3d%3d
Any promotion of anti-vaccination statements or health advice which contradicts the best available scientific evidence or seeks to actively undermine the national immunisation campaign (including via social media) is not supported by National Boards and may be in breach of the codes of conduct and subject to investigation and possible regulatory action.”
“Fully vaccinated people with Delta variant breakthrough infections can spread the virus to others. However, vaccinated people appear to be infectious for a shorter period: Previous variants typically produced less virus in the body of infected fully vaccinated people (breakthrough infections) than in unvaccinated people. In contrast, the Delta variant seems to produce the same high amount of virus in both unvaccinated and fully vaccinated people. However, like other variants, the amount of virus produced by Delta breakthrough infections in fully vaccinated people also goes down faster than infections in unvaccinated people. This means fully vaccinated people are likely infectious for less time than unvaccinated people.”
     - “Among five COVID-19 patients who were hospitalized, four were fully vaccinated; no deaths were reported.”
     - “Real-time reverse transcription-polymerase chain reaction (RT-PCR) cycle threshold (Ct) values in specimens from 127 vaccinated persons with breakthrough cases were similar to those from 84 persons who were unvaccinated, not fully vaccinated, or whose vaccination status was unknown (median = 22.77 and 21.54, respectively).”
[32] Pfizer/Moderna
On June 21st, FDA “announced revisions to the patient and provider fact sheets for the Moderna and Pfizer-BioNTech COVID-19 vaccines regarding the suggested increased risks of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the tissue surrounding the heart) following vaccination.”
AstraZeneca
The TGA has confirmed on their weekly reports that 7 deaths occurred from AZ vaccination https://www.tga.gov.au/periodic/covid-19-vaccine-weekly-safety-report-19-08-2021 6 were Thrombosis with thrombocytopenia syndrome (TTS) and 1 from one was a case of immune thrombocytopenia (ITP).
[33] Who are the vulnerable:
     - According to The World Health Organisation, the vulnerable and high risk groups are: “people who are older than 60 years or who have health conditions like lung or heart disease, diabetes or conditions that affect their immune system.‚Äč” https://www.who.int/westernpacific/emergencies/covid-19/information/high-risk-groups
     - The Australian Health Department state: high risk of severe illness are 70 years and over, immune suppressive therapy, blood cancer, chemo or radio therapy, lung or heart disease, diabetes, neurological conditions, chronically inflammatory conditions, etc. https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/advice-for-people-at-risk-of-coronavirus-covid-19#who-is-at-high-risk-of-severe-illness-
     - According to the ABS reported October 2020, out of 682 deaths in Australia deemed “COVID-19” deaths, 496 of them had pre-existing chronic conditions and 8 of them were suspected COVID-19 but the presence of the virus was not confirmed https://www.abs.gov.au/articles/covid-19-mortality-0 . “Among these 496 deaths, dementia was noted on 41% of death certificates, chronic cardiac conditions on 32%, diabetes on 17% and hypertension on 16%” https://www1.racgp.org.au/newsgp/clinical/more-than-70-of-covid-19-deaths-had-pre-existing-c
“By contrast, Israelis who were vaccinated were 6.72 times more likely to get infected after the shot than after natural infection, with over 3,000 of the 5,193,499, or 0.0578%, of Israelis who were vaccinated getting infected in the latest wave.”
[35] Robert Booy, COVID-19 and vaccination in children: https://insightplus.mja.com.au/2021/29/covid-19-and-vaccination-in-children/
[38] https://papers.ssrn.com/sol3/papers.cfm?abstract_id=3897733 "Breakthrough Delta variant infections are associated with high viral loads, prolonged PCR positivity, and low levels of vaccine-induced neutralizing antibodies, explaining the transmission between the vaccinated people.”
[40] Gold Coast University Hospital infectious diseases physician Dr John Gerrard From “The Weekend Australian” 27-29 Feb. 2021, https://www.theaustralian.com.au/wp-content/uploads/2021/02/C19-Vaccine-Report-final.pdf Column 4-5 below
 
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