The Safe Vaccine Debate – 1. Dr Judy Wilyman Report – Open Letter & Newsletter #197 2. Robert Kennedy’s World Mercury Project: Merck Accused of Fraud, Deceit and Negligence in US Gardasil Case 3. Elizabeth Hart: OverVaccination

1. Dr Judy Wilyman Report – Open Letter & Newsletter #197

Copied to the Australian Medical Association, UOW Vice-Chancellor, Paul Wellings and UOW Academics/Staff

Dear Concerned Australian Community,

As our letters to politicians, the Human Rights Commission and  UOW academics over the last two decades have been ignored, and UOW academics have signed their names to false information about the safety and efficacy of vaccines, without being required to investigate this science, I am forwarding you this email exchange regarding the 2GB talk on vaccinations and questions that Dr. Tony Bartone, (AMA) has been asked to answer.

I will forward you the response from Dr. Tony Bartone when he provides one. 

To date Australia has banned Dr. Sherri Tenpenny, Kent Heckenlively and Polly Tommey, from coming to Australia to tell you the truth about vaccines. The Australian government is censoring my university research on vaccines and the Australian media has misinformed you about my vaccination research.

And the University of Wollongong is allowed to remain silent. 

My UOW research demonstrates with evidence the lack of safety and efficacy of vaccines and the disregard for the genetics of the Australian population. The UOW Vice-Chancellor, Paul Wellings has stated UOW is standing by my research (PhD thesis ) 

Compulsory vaccines in Australia will ensure there is a market for the 200+ vaccines that are currently being developed. Yet Australian doctors are not required to tell their healthy patients what is in the vaccines or what serious adverse health events have been listed on the pharmaceutical prescribing information leaflets – for decades. And Australia does not have a Vaccine Injury Compensation Program similar to the US and other countries, that legitimises the harm that vaccines cause to our children and ourselves.    

We do not want a vaccine-injury compensation scheme we want the right choose which vaccines we use without losing any rights or financial benefits.

Please read the information below and the questions that have been asked of Dr. Tony Bartone from the AMA, and ensure that you get involved in this debate to protect the health of children and university students, whose right to choose which vaccines they use and when HAS ALREADY BEEN REMOVED IN AUSTRALIA.

This policy will be extended to all adults in the near future unless the public stops the lies that are being told to politicians. 

Kind regards,

Dr. Judy Wilyman ( )

Newsletter 197 Health Minister, Greg Hunt, and Censorship of the Vaccination Debate in Australia
20 April 2018

The Health Minister, Greg Hunt, claimed yesterday on ABC radio that he believes in freedom of speech yet he is currently attempting to shut down the public debate on vaccination. Our right to choose how many vaccines we use in our bodies is being removed in Australia yet there is no discussion of this issue in the mainstream Australian media.

In November 2017 the City of Sydney Council stated that it would not allow my university research on vaccination to be presented or advertised in council venues. This is despite the fact that the University of Wollongong stands by this research.   

Traditionally, it is academic debate of university research that forms the basis of government public health policy, but not any more. Australia’s Health Minister, Greg Hunt, has stated he will shut down social media sites that are presenting the risks of vaccines because he has defined this as ‘anti-vaccination‘.

Instead of describing this as a debate of the medical risks and benefits of vaccination, we have a health minister who is dismissing the risks as ‘anti-vaccination‘.

This is harmful to the Australian population because Greg Hunt is preventing the science from being scrutinised by the Australian public. This is particularly concerning because vaccines are drugs for healthy people and they cannot be guaranteed ‘safe’ in any genetically diverse population.

Hence Australia’s mandatory and coercive vaccination policies implemented in social welfare legislation represent a crime under the Nuremberg Code.
This is the reason why Sweden and Colombia have stated they will not adopt these policies.

Greg Hunt, and Richard Di Natale (the Greens Leader) are being informed on this issue by powerful lobby groups (SAVN / Australian Skeptics Inc / Friends of Science in Medicine) who are providing false information about the safety and efficacy of vaccines based on corporate-sponsored research that is published in corporate-sponsored journals and presented to the public by a corporate-sponsored media.  

I described this situation in Chapter 6 of my PhD thesis in 2015 and now in 2018 here is an article in the Daily Mail titled Top Medical Journals accused of Skewing Research by raking in Millions of Dollars in ‘Bribes’ from Drug Firms‘ (13 April 2018)  

In the 1950’s doctors were using flawed ‘tobacco science’ to promote cigarettes to the public as ‘safe’ and this was finally exposed as ‘pseudo-science’. This same science is now being used to promote vaccines and this is why Australian pubiic health authorities will not debate this science.

Our health ministers are working hard to censor this debate because the science that is being used to support government legislation will not stand up to scrutiny – it is tobacco science‘. 

Judy Wilyman PhD
Bachelor of Science, University of NSW
Diploma of Education (Science), University of Wollongong
Master of Science (Population Health), Faculty of Health Sciences, University of Wollongong.
PhD in The Science and Politics of the Australian Government’s Vaccination Program, UOW School of Humanities and Social Inquiry.


2. Robert Kennedy’s World Mercury Project: Merck Accused of Fraud, Deceit and Negligence in US Gardasil Case
Apr. 25th, 2018

By Christina England, BA Hons, for GreenMedInfo, Partner of World Mercury ProjectMerck’s aggressive agenda to increase HPV vaccine uptake rates, despite causing thousands of severe injuries, is hitting a stumbling block in a court case alleging blatant corruption.There has been documented evidence that the HPV vaccine has caused more injuries than any other vaccination in history. Despite this evidence however, the HPV vaccination has continued to be hailed a success by the pharmaceutical industry and governments alike.According to the World Health Organisation’s (WHO) VigiAccess database, as of April 09, 2018, a total of 85,329 reports of adverse reactions have been filed regarding the HPV vaccination. These reports include 37,699 reports of nervous system disorders; 2450 cardiac disorders, (including 38 cardiac arrests) 533 reports of Postural orthostatic tachycardia syndrome (POTS); over 3200 reports of seizures or epilepsy, 8453 syncope and 389 deaths.In July 2016, a case was filed in the Superior Court of the State of California, Los Angeles County (central district). The case involved a 16-year-old female who between 2010 and 2011 received three injections of Gardasil, the HPV vaccination manufactured by Merck. Shortly after she received her third vaccination, she suffered a severe adverse reaction, the nature and complexity of which, failed to be diagnosed until 2015, when she finally received the diagnosis of Postural Orthostatic Tachycardia Syndrome (POTS).For those of you who are unaware, Postural Orthostatic Tachycardia Syndrome (POTS) is an abnormal response of your body when you are upright (usually when standing). It is caused by a problem with the nervous system which controls the autonomic functions in the body. This part of the nervous system is called the autonomic nervous system.The symptoms of POTS occur when you are upright and are relieved when lying down. These symptoms are associated with an abnormally high and persistent increase in heart rate within ten minutes of standing.  (Description of POTS taken from Patient Access website)If this diagnosis was not devastating enough for this young lady and her family, in 2016, she was further diagnosed with an underlying small fiber neuropathy, existing within and throughout her body.

Her family firmly now believe that the vaccinations caused her illness because prior to receiving the HPV vaccination, she was physically active, and had not only participated in her high school basketball team but had also engaged in other athletic activities.

It is for this reason, that the family decided to file a case against the manufacturer of the vaccine, Merck, accusing them of:

1. Fraud and Deceit
2. Negligent Misrepresentation
3. Defective Product – Inadequate warnings & information
4. Medical Malpractice
5. Medical Battery

As you can see these charges are extremely serious and if won, this case would set a precedent for similar cases to be brought against the manufacturer of this vaccine in the future.

Merck had wrongfully and deceitfully failed to perform in the preapproval processing period and thereafter, the material scientific and medical investigations and studies relating to the safety, effectiveness and need for the Gardasil vaccine as required by and under the FDA directives and regulations.

Merck Accused of Fast Tracking a Vaccine for Financial Gain

The complaint outlined the fact that the Plaintiff and her family believed that Merck had wrongfully and deceitfully failed to perform in the preapproval processing period and thereafter, the material scientific and medical investigations and studies relating to the safety, effectiveness and need for the Gardasil vaccine as required by and under the FDA directives and regulations.

It is a well-known fact, that all pharmaceutical products must undergo extensive pre-marketing clinical trials often spanning several years before the FDA can consider the product for licensing.

The complaint written by the family’s attorney stated that:

Upon approval by the FDA of the Gardasil vaccine, Defendants Merck, Does 1 through 25, and each of them commenced and engaged in highly extensive, and aggressive marketing practices, which were designed primarily, if not solely, to increase the sales and profits from Gardasil.In doing so, Defendants Merck, Does 1 through 25, and each of them, in order to preclude any and all questions by consumers, patients and others, as to the effectiveness, safety and need for the administration of the Gardasil vaccination as well as the risks of serious adverse reaction related thereto, intentionally, wrongfully and deceitfully withheld, failed to provide and concealed from consumers, patients and others material facts and information with respect to the effectiveness, safety and need for the administration of the Gardasil vaccination, as well as the risks of serious adverse reaction related thereto and as in part hereafter set forth.” (emphasis added)

The complaint continued by describing each and every misdemeanour that Merck was thought to have participated in. It stated:

“Further, Defendants Merck and Does 1 through 25 in its Marketing wrongfully and deceitfully failed to unambiguously inform those to whom the marketing was directed, of material facts and information which they knew or should have ascertained through their investigations and studies specific to risk/ benefit and quantitative risk assessments regarding and including, among other things, the following:

1. The five-year period that the Gardasil vaccine was then only known to be effective;
2. That Gardasil was effective only as to certain and not other strains of the HPV virus;
3. The Gardasil vaccine is not effective once an individual is infected with the HPV virus;
4. Other existing methods that are effective in avoiding HPV viral infections;
5. The minimal risk that even once the individual was infected with the HPV virus the infection would result in precancerous lesions;
6. The successfulness of exiting methods of diagnosing and treating HPV precancerous lesions;
7. The successfulness of exiting methods of diagnosing and treating any resulting cancer;
8. The nature as the consequences of serious adverse reactions to the HPV vaccine; and
9. Other items related and material to risk/benefit and quantitative risk assessments not now known and if required leave of Court will be requested to amend this complaint to set forth fully such item or items when ascertained.

Such information was and is reasonably required by patients and consumers as well as others when considering and deciding whether or not under their individual and personal circumstances to be vaccinated with Gardasil.”

Not only did the family and their attorney outline an excellent and well thought out case, they went one step further and suggested that the court hold a Science Day Hearing.

So, what did both sides offer in the way of science to support their case and did the Judge agree to his unusual request?

Judge Agreed to a Science Day Hearing

In an unusual step the Judge in this case, agreed to hold a “Science Day Hearing” to enable the court to get a better understanding of the science behind the HPV vaccine. In advance of the scheduled science day presentation both parties submitted briefs that outlined their side’s view of HPV vaccine science.

In other words, for the first time ever, both sides including the vaccines manufacturer Merck, were given the unique opportunity to present to the court, their up-to-date science and studies proving the safety and effectiveness of this vaccine. The information provided would prove once and for all, whether or not Gardasil was not only a safe vaccination but necessary in the fight against cancers caused by the HPV virus.

What Science Did the Two Sides Present?

The paperwork that was submitted clearly demonstrated many of the issues surrounding HPV vaccines and vaccination policies. The Plaintiff’s submission, offered clear precise facts to enable the Judge to understand the science behind the vaccination.

Their submission contained the following information:

“There are approximately 130 strains of the HPV virus, of which only 15 to 18 strains are known to be associated with cervical cancer.  The Gardasil vaccine provides protection against only 4 specific strains, namely HPV 6, 11, 16 and 18.  Strains 16 and 18 are thought to be casually associated with 70 % of the worldwide HPV related cervical cancers.  HPV 6 & 11 are associated with warts.

As stated, ninety-five (95%) percent of HPV infections are removed from the body by its own immune and related processes without medical or other consequences. Any abnormal cell growth associated with the remaining 5%, approximately 20% (1% of the total), if not identified and removed could be at risk of developing into cancerous cells in approximately 5 years which could progress to irreversible cancer in 15 to 30 years.  The incidence of cervical cancer occurring in the United States is estimated to be 1.4 to 2.3 per 100,000. The risk of precancerous cells, due to the presence of the HPV 16 and 18 viruses, progressing to cervical cancer is estimated at 1.5 per 100,000.  The actual incidence rate of serious adverse events after HPV vaccination is unknown.”

They outlined a brief history of the immune system and how it works and continued by describing the nature of the autoimmune diseases that the injured teenager was now suffering from.

To support their argument, they included a wide range of scientific studies that had been written by some of the world’s leading experts and they criticized Merck for ‘misleading the public’ in their advertising campaign.

They stated that:

“Initially, qGardasil (Quadrivalent Gardasil) is not a treatment process and does not prevent cancer as marketed by Merck. Gardasil is a vaccine designed to increase the response of the Human Immune system to pathogens namely HPV viruses 6, 11, 16 & 18.”

They continued:

“Generally, with vaccines an adjuvant is required to be injected as a part of the vaccine to increase the body’s immune response to the antigen (disease causing organism).  The most commonly used adjuvants for many years have been aluminum salts with an Aluminum hydroxide base.

It is medically and scientifically accepted that aluminum salts are toxic to and damage the human cells at the injection site.  In addition, the aluminum salts cause inflammation at the site.  These aluminum salts may bind with the free DNA released from the damaged and dying cells at the injection site.  The combination of the Aluminum salt bound by the human DNA is effective in activating Toll Like Receptors (“TLR”), whose function in the immune system is highly complex.”

Their submission concluded that:

“The foregoing is merely illustrative of the complex and extensive scientific factors involved in this litigation.  Although the purpose of Science Day is to provide the Court with information as to the nature and extent of the complex scientific matters involved, it is necessary to connect these matters to a foundation rooted in the facts of the case before the Court, which may be construed as argument.

Scientific issues not addressed in this Brief, which are relevant to the safety, efficacy/effectiveness, need and risk/benefits of qGardasil include, without limitations, the following:

1.  Fast tracking of the FDA approval process to a 6-month period when criteria for fast tracking were not met.
2.  Five-year effectiveness of qGardasil as of 1/1/2011, now believed to be 8 years.
3.  Use of end points which did not establish the effectiveness of qGardasil.
4.  Effect on the clinical trial analysis of the removal of participants experiencing adverse and serious adverse events.
5.  The effect of non – HPV 16 and 18 cancer producing strains on cervical cancer occurrence when HPV 16 and 18 are eliminated.
6.  Lack of adequate pediatric clinical testing of the qGardasil regarding potential ovarian disorders/failures.
7.  The effect of clinical testing and studies involving undeveloped countries on U.S. analysis.”

In comparison, Merck appeared to offer very little in the way of scientific evidence to support their argument. Merck wrote:

“At Science Day, Merck intends to provide the Court with:
(1) an overview of The National Childhood Vaccine Injury Act of 1986 and the National Vaccine Injury Compensation Program, and their impact on the present litigation;
(2) background information about the development and approval of vaccines and, specifically, Gardasil, in the United States; and
(3) a detailed review of the extensive safety data that established and has continually reaffirmed the safety profile of Gardasil.”

They continued with what appeared to be an attempt to divert the Judge’s attention away from the science by switching the focus onto the Plaintiff’s unfortunate delay in obtaining a diagnosis:

“Although plaintiff alleges a moving target of injuries and purportedly related symptoms, Merck’s Science Day presentations will address the three on which plaintiff currently seems most focused; autoimmune diseases, demyelinating diseases, and Postural Orthostatic Tachycardia Syndrome (‘POTS’). A preview of the data concerning Gardasil and these conditions is set forth herein.”

This, in our opinion, failed to address the main points of the case that had been put forward by the Plaintiff and we found it extraordinary, that given this unique opportunity, Merck offered the Judge very little in the way of scientific evidence.

In fact, throughout Merck’s submission, instead of presenting the court with evidence from the Phase 1,2,3 and 4, pre-licensing vaccination trials, that should have preceded the vaccination coming onto the market, Merck appeared to rely heavily on post-marketing evidence from the VAERS website, the CDC, the FDA and other similar organizations.

Furthermore, instead of producing any real science as one would expect, Merck chose to use part of their unique opportunity, to discredit SaneVax Inc, an organization dedicated to providing the public with scientific facts and evidence behind vaccination safety.

Another interesting point that we discovered on reading Merck’s scientific day submission, was that their submission contained a large amount of information that appeared to focus on proving that Gardasil did not cause the teenager’s condition, instead of concentrating on the task at hand.

It will be interesting to see the final outcome of this case and we wish the family and their attorney, every success in their endeavour to get justice for this young lady’s injuries.

To learn more about the underreported harms of HPV vaccine, view our database on the topic here. To learn about the unintended, adverse effects of vaccinations in general, view our database on the topic here.

© April 17, 2018, GreenMedInfo LLC. This work is reproduced and distributed with the permission of GreenMedInfo LLC. Want to learn more from GreenMedInfo? Sign up for the newsletter here:

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3. Elizabeth Hart: OverVaccination

Hi All, I’ve just watched the speech by Robert F Kennedy Jr on the World Mercury Project homepage:  

The video is also on Facebook:

This is a great, motivating speech.  
We all know how difficult it is to work on the vaccination project, with times when it seems futile to be challenging the hegemony of the vaccine industry and its acolytes in academia, the medical ‘profession’, government and the media.
Watching RFK Jr’s speech today motivated me to soldier on. I’ve taken the liberty of providing an emphasised transcription because it’s useful to keep and refer to, i.e.:
A passionate, motivating speech.
But there’s a drawback with the apparent limitation of the project, i.e. the World Mercury Project, as there are many ingredients in vaccine products that may cause harm, e.g. aluminium, fetal bovine serum etc. 
I see that the Vaccine Safety Project title is also being used – should this now be the dominant title of the project to fully reflect the multiple concerns about vaccine products?
And of course there’s the sheer gross over-use of these vaccine products that must be considered, are we heading towards the destruction of natural immunity for future generations, it’s mind-boggling to think about what this might be leading to…?  The problems of the over-use of other medical products such as antibiotics, opioids, anti-depressants etc are being acknowledged, but vaccine products continue to be kept on a pedestal, without effective independent and objective scrutiny, so many of the so-called ‘experts’ in this area are conflicted by their associations with the vaccine industry. 
Where can citizens turn to for serious consideration of international vaccination policy, which is currently being run by the vaccine industry, aided and abetted by the Murdoch media, Bill Gates and others?


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