Indoctrination: The True Risks and Benefits of Vaccines

August 17, 2021, By Judy Wilyman PhD

This article describes how the medical-industry paradigm has provided false and misleading information about vaccines to global populations for decades. Through its control of the education system, both doctors and research institutions, and through the mainstream media, it has been working towards this outcome for over 3 decades.  This has resulted in agnotology: populations that are ignorant of the real risks and benefits of vaccines. In addition, I will provide evidence that there is no legitimate public health purpose for coercive vaccination because governments have not adopted these laws in any Health Act with scientific evidence to support them.

Over the last 70 years the national immunization programs (NIP) of all countries have expanded as the World Health Organization (WHO), advised by the Global Alliance for Vaccine Initiatives (GAVI), took control of the design of Global Health Policies. In Australia, as in many countries, this program expanded to include recommendations for 16 vaccines (~52 doses) in the NIP for children 0-14 years of age.

In 2016 Australia mandated the NIP in Social Services policies, but not in any Health Act in Australia. This allows the Australian Prime Minister to claim that ‘vaccines are not compulsory’ even though social services programs and businesses can coerce parents with their jobs, childhood education, welfare benefits, and travel. In other words, parents must ‘choose between using a drug or having the capacity to live in society. Is this a real choice? These policies were implemented in Australia in 2016 under the title “Choices for Families”; these are policies that removed real choices for families, but they were promoted by the Australian government as creating choices for families.

These coercive vaccination policies have not been implemented in Australia in any Health Act because the government has not provided any scientific evidence to validate coercive vaccination policies as being for a legitimate public health purpose. If there is no health law to validate coercive vaccination, then governments are breaching all International Human Rights Covenants and medical ethics with these policies in social services legislation.

These social services policies remove parents right to welfare benefits, jobs, education, and travel. That is, they are losing their inalienable right to live in society without any scientific evidence being provided by the Australian government in any Health legislation. In addition, neither medical doctors or their patients are informed of the ingredients of vaccines and the risk of chronic illness that appears months or years after the vaccine is given.

Did you know that antibiotics are in most vaccines? Many people are allergic to antibiotics, and using any vaccine carries the serious risk of anaphylactic shock to this and many other vaccine ingredients. Are you being informed of this before you give consent to the vaccination of your baby or yourself?

Please consider whether you want the substances listed below injected into the tissues of your newborn infant before its body systems are fully developed – including the blood brain barrier.

The ‘new norm’ in children’s health since coercive vaccination policies were implemented in the 1990’s (when doctors were paid in Australia for each vaccine that was administered), includes – allergies, anaphylaxis, Kawasaki’s Disease (vasculitis), Chronic Fatigue Syndrome (CFS), autoimmune disorders (diabetes, childhood rheumatoid arthritis, arthritis, multiple sclerosis etc.), thrombocytopenia purpura (ITP), autism, speech delay, neurological disorders, encephalopathy, meningitis, ADHD, cancers, and many more that have increased in direct correlation to the vaccination program – a plausible cause of this illness . Whilst correlation is not causation a fundamental principle of evidence-based medicine is investigating all correlations before a drug is declared safe and effective to consumers.

This lack of investigation allows doctors and governments to claim, ‘we don’t know what causes these illnesses’ and ‘it would have developed anyway.’ Here is further evidence of the possible causal link between vaccines and autism. Here is the evidence that the CDC cannot support its claim that vaccines do not cause autism.

Your doctor will also inform you that the illness is ‘just a coincidence’ after vaccination because the Australian government and vaccine manufacturers have never funded a causality study that would prove this association. That is, a study that uses an inert placebo in the unvaccinated trial group to prove the safety of each vaccine over an appropriate long-term period: a period that includes the delay in the appearance of these diseases (5-10 years), or even the safety of combining 16 vaccines in the human body. That is, governments are assuming they are safe without any hard evidence to prove it. This is called ‘undone science’ and it is described in my PhD thesis.

Governments don’t have to prove the safety of these drugs because the pharmaceutical companies received indemnity for any vaccine product in the US Congress in 1986. The pharmaceutical companies needed to get indemnity in the 1980’s because they were paying millions of dollars in compensation every year for deaths and injuries due to vaccines. Does this evidence support the claim that vaccines are a ‘lifesaving drug’  ?

This removal of liability was achieved by deliberately creating fear to influence Members of Congress and the public at the time. Since 1986, as a result of this indemnity for vaccine manufacturers, governments have misused the precautionary principle in the design of vaccination policies. The precautionary principle was designed to protect the public’s health in the design of government public health policies. This principle can only protect ‘health’ in these policies if the onus of proof of harmlessness is on the proponent of the technology and not the public.  However, since 1986 the onus of proof of harmlessness has been reversed and it is has been placed on the public. In this format, it is protecting industry-interests in government policies, and not the public’s interest of health because any evidence the public provides can be ignored.

This is the case even though the public has been informed that vaccination policies are designed to ‘protect community health’. The community is trusting the government to be carrying out its duty of care to its citizens in protecting health in the design of public health policies. Yet by reversing the onus of proof, and by allowing serious conflicts of interest in government vaccine advisory boards, the government is protecting the industry-interests of profits in these policies. This is described more fully in my article ‘Misapplication of the Precautionary Principle has Misplaced the Burden of Proof of Vaccine Safety.’

Despite the medical industry’s knowledge that hundreds of chronic illnesses are linked to our genes (epigenetics), doctors, governments, and the media have been downplaying the risks of vaccines and exaggerating the benefits for decades.

This is how the indoctrination of the population has occurred, which strives for every individual to believe vaccines are only beneficial. A situation that is now leading to people taking the COVID ‘vaccine’ (for which there is no proven benefit and many proven risks) and even though the new genetic technology has never been tested in human clinical trials. Plus, in the small animal studies that were done, all the animals died upon re-exposure to wild coronaviruses. This is called Pathogenic Priming or a hyper-immune response. The effects of pathogenic priming are more clearly explained by Dr. James Lyons-Weiler PhD and Robert F Kennedy Jnr in this article in The Defender.

For thirty years the public has been educated with false and misleading health information from the industry-medical paradigm and from the mainstream media. The result is agnotology – a society that has been educated to be ignorant about the risks and benefits of vaccines.

Below are some of the common components of traditional vaccines that are not inert substances that doctors and consumers are not informed about before vaccines are given:

Antibiotics: Neomycin, Polymyxin, Gentamicin, Kanamycin

Foreign Protein includes:

Human Foetal Cells

Chick embryo Cells and Bovine Serum

Recombinant Human Albumin (genetically engineered DNA)

Potassium Chloride

Aluminium hydroxide

Aluminium hydroxide/phosphate

Aluminium phosphate

Thimerosal (50% mercury compound) (flu vaccine multidose vials & infanrix-hexa & hep B 2013)

Borax (‘sodium borate’ – causes infertility and is found in HPV vaccines and hep A)

Polysorbate 80 – causes infertility


Egg protein



Monosodium glutamate (MSG)



Filed Under: Children’s HealthImmunisation Policymedia misinformationNo Jab No Pay Policyvaccination

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  1. what a fantastic informative article. Has Dr Wilyman still got her job? I have always wondered how being injected with poisons can heal viruses, etc. And as usual there is the money factor.

    Cyanide, formaldehyde, catechins, flavanols, quercetin, epicatechin, procyanidins, phlorizin, starch, potasium, manganese, iron, copper, zinc, phosphorous, chloride, sugars, dihydrogen monoxide (and more).


  3. Yes, at this point she still has her job, she gave us all (if you attended the Perth 31/08 rally outside WA Parliament) great support and basically discussed in further detail all the above article. The attendance 400-500 although small was very vocal. Please all of you support the protests on 18th September, all voices count.

  4. COVID VACCINES – DIRE WARNINGS in this Paper by Seneff & Nigh – damage from these vaccines is potentially catastrophic and transgenerational – and now they have targets on our children.
    The rats will be scurrying from an exploding ship when the population learn the true facts of these shocking experimental covid vaccines – please read these papers – I note today, that already as at 16.9.2021 23,751,922 of these experimental jabs have been coerced/forced on Australians and being mandated for ever increasing population sectors – this grossly violating universal informed consent codes.
    Also Paper from Classen Immunotherapies.

    PLEASE READ THESE PAPERS AS OUR POLITICIANS are incapable of (allegedly) independent and unbiased research as their extreme pro-vaccination lobby involvement/stance proves and allegedly throughout the entire Australian Government Vaccinations Policy is rife with Conflicts of Interest -it’s shocking and they are answerable to no one. Likewise – who in the hell allowed mainstream media empires to be calling the shots and virtual mouthpieces for Pharmaceutical Industry (allegedly) – WRONG WRONG WRONG. They all have to be stopped. Read the Papers – the DIRE WARNINGS.


    Worse Than the Disease? Reviewing Some Possible
    Unintended Consequences of the mRNA Vaccines
    Against COVID-19
    Stephanie Seneff and Greg Nigh
    Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge MA, 02139, USA, E-mail:
    Naturopathic Oncology, Immersion Health, Portland, OR 97214, USA
    Operation Warp Speed brought to market in the United States two mRNA vaccines, produced by Pfizer and
    Moderna. Interim data suggested high efficacy for both of these vaccines, which helped legitimize Emergency Use Authorization (EUA) by the FDA. However, the exceptionally rapid movement of these vaccines through controlled trials and into mass deployment raises multiple safety concerns. In this review we first describe the technology underlying these vaccines in detail. We then review both components of and the intended biological response to these vaccines, including production of the spike protein itself, and their potential relationship to a wide range of both acute and long-term induced pathologies, such as blood disorders, neurodegenerative diseases and autoimmune diseases. Among these potential induced pathologies, we discuss the relevance of prion-protein-related amino acid sequences within the spike protein. We also present a brief review of studies supporting the potential for spike protein “shedding”, transmission of the protein from a vaccinated to an unvaccinated person, resulting in symptoms induced in the latter. We finish by addressing a common point of debate, namely, whether or not these vaccines could modify the DNA of those receiving the vaccination. While there are no studies demonstrating definitively that this is happening, we provide a plausible scenario, supported by previously established pathways for transformation and transport of genetic material, whereby injected mRNA could ultimately be incorporated into germ cell DNA for transgenerational transmission. We conclude with our recommendations regarding surveillance that will help to clarify the long-term effects of these experimental drugs and allow us to better assess the true risk/benefit ratio of these novel technologies.
    Full Paper >

    COVID-19 RNA Based Vaccines and the Risk of Prion Disease
    Classen Immunotherapies, Inc., 3637 Rockdale Road, Manchester
    MD 21102, E-mail:
    J. Bart Classen, MD*
    Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARSCoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing. In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients. The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations. In the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified. Two GGΨA sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration.
    The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.
    The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit.
    Full Paper >