I have personally interviewed vaccinators at three COVID19 Vaccination Centre’s. Each individual vaccinator was questioned “If I have a COVID19 jab will you promise I will not have a serious adverse event or die from receiving the COVID19 jab”? In total 10 vaccinators each informed me that the COVID19 Vaccine is extremely safe.

True informed consent is a process, and, as such, it requires that the health-care provider enter into a discussion that ultimately leads to the patient understanding of their options, and the risks and benefits of the alternative courses of action.

New Zealand Bill of Rights 1990 states the ‘Right to refuse to undergo medical treatment. Everyone has the right to refuse to undergo any medical treatment.
The New Zealand Bill of Rights 1990 is referred to in the COVID19 Public Health Response Act Section 11– The right to refuse to undergo medical treatment.
The Code of Health and Disability Services Consumers’ Rights – There is no particular age at which children or young people may give informed consent under the Code.

A HUMAN RIGHTS APPROACH TO HEALTH:
– Accessibility- non-discrimination, physical accessibility, economic accessibility (affordability), information accessibility.
– Acceptability: respectful of medical ethics and culturally appropriate, sensitive to age and gender
– Quality: scientifically and medically appropriate

All people have the Right to Self-Determination. The historical and current development of the right to self-determination on the basis of the Charter i of the \ United Nations and other instruments adopted by United Nations organs, with particular reference to the promotion and protection of human rights and fundamental freedoms.

The Charter of the United Nations expressly establishes the right to self-determination.
Guaranteeing informed consent is fundamental to achieving the enjoyment of the right to health through practices, policies and research that are respectful of autonomy, self-determination and human dignity. Safeguarding informed consent along the health-care continuum is an obligation placed on States and third parties

The concept of consent has evolved for centuries to arrive at its current meaning. In the aftermath of the Nuremberg Trials, increased international recognition of patients’ rights developed in the twentieth century, hence defining the responsibility of health-care providers and States responsibilities to the patient.

In 1947, the Nuremberg Code asserted that the voluntary consent of the human subject to medical research is necessary under all circumstances. The Declaration of Helsinki (1964) further developed the Code principles and tied them to the ethical duties of physicians, as outlined in the Declaration of Geneva (1948).
In 1994, the World Health Organization Amsterdam Declaration on Patients’ Rights required informed consent as a prerequisite for any medical intervention, guaranteeing also the right to refuse or halt medical interventions.

Informed consent is not mere acceptance of a medical intervention, but a voluntary and sufficiently informed decision, protecting the right of the patient to be involved in medical decision-making, and assigning associated duties and obligations to health-care providers. Its ethical and legal normative justifications stem from its promotion of patient autonomy, self-determination, bodily integrity and well-being.

I am extremely concerned that young people in New Zealand can legally consent to participating in Clinical Trials without prior parental or guardianship consent. That they can also book a COVID19 jab online, or just turn up at a COVID19 Vaccination Centre, and are not be required to provide identification of proof of age.

The randomised Pfizer Clinical Trial (Human Experiments) was of 2,260 12 – 15year olds from across America. 50% of them were jabbed with a placebo, only 1,130 actually received the COVID19 jab. This is a very tiny percentage of the population within this age group considering there are almost 17 million 12-15 year olds in America alone and only 1,130 participants were required for FDA to give consent.

COVID 19 so called vaccines are not vaccines, they are inoculations. They do not stop infection, they are an immune treatment.
I am extremely concerned for our young people who have the legal right to consent to be participants in these human trials, human experiments. (12-15yrs old).
DHB’s are trying to get schools on board for onsite vaccination clinics.

Chris Hipkins has reported that COVID19 Vaccinations for children from the age of 5years will be rolled out by the end of January 2022 as FDA have given Pfizer provisional consent for these inoculations, they are just awaiting MEDSAFE approval.

Globally populations are being controlled by a Communist Chinese type Social Credit System of Rewards and Punishments, compliant or non-compliant our freedoms, human ights, civil liberties have been severely violated, it now appears that all these Human Rights just simply, sadly disappeared. We really do not have any Human Rights.

NOTE: FOR FURTHER INFORMATION PLEASE CLICK ON THE IMAGE ABOVE WHICH WILL TAKE YOU TO MY RUMBLE VIDEO.

The Imperial Global Public-Private Corporate Governance of the Planet namely Earth. The Eco-Political Global Elite (The Green Leftist-Socialist-Communist Global Powerhouse)

The Corporate capture of global governance : The World Economic Forum – UN partnership agreement is a dangerous threat to all living beings on the earth. Digital Globalization, digital Data, digital control of global populations. A Multistakeholder business governance, nationally-globally is being played out, has been planned for years, the end is in sight. The emerging powers in this Global imperialist global governance.

A group of rising powers from the global South is effectively challenging western predominance, the hallmark of the global order over the last two centuries. CIGI’s research is built on long term transnational networking that brings together high-ranking scholars from the industrialized and the developing worlds. The redistribution of wealthy and the end of private property rights.

THIS IS TOO SAD, TOO CRUEL IT MUST NEVER BE…..
Where have all the farmers gone..long time passing.
Where have all the tradies gone…long time passing…
Where have all the small businesses gone…long time passing
Where have all our freedoms gone….long time passing.

WAKE UP NEW ZEALAND NOW

Through social media I cam across a post that referred to a dangerous chemical namely Ethylene Oxide being used in PCR tests as a sterilization agent. This caused me some serious concern, therefore I decided to dig a bit deeper into this chemical namely Ethylene Oxide.

The FDA Is Taking Steps to Move Beyond Ethylene Oxide “Gas” Sterilization. There has been calls to replace Ethylene Oxide because of cancer risks

There’s outrage from exposed communities has federal regulators and device makers seriously rethinking a question that’s been hanging over the sterilization industry for decades: Can ethylene oxide be replaced?

Ethylene oxide is a widely used chemical made in the U.S. by some of the industry’s global giants, including Dow Chemical, Huntsman, Shell and Union Carbide. The main ingredient in automobile antifreeze.

FDA reported they will l continue in its efforts to reduce over-reliance on ethylene oxide for medical device sterilization. Supply issues can lead to shortages of medical devices—and can pose a threat to public health by delaying or disrupting critical care for patients. Mitigating product supply issues and working to prevent patient harm from device shortages are important to the FDA.

November 2019 it was reported that regulators from public health agencies, medical device manufacturers and expert physicians gathered at a 2 day meeting to discuss, address challenges with ethylene oxide, a carcinogenic gas used to sterilize more than 50% of medical devices.

The topic of focus of those at the gathering was “What’s the potential impact of reducing, eliminating or replacing ethylene oxide sterilization on the medical device supply chain, and what can FDA do to prevent shortages of critical devices used by hospitals and other healthcare providers across the country”?

Back in 2019, it was documented that 20 billion to 25 billion devices are sterilized in 2018 using ethylene oxide. FDA issued a warning in October 2019 that without adequate availability of Ethylene Oxide a national shortage of devices will occur.

Clinical Oncology News in the US, May 2nd 2020’s article read ‘Sterilization has beena problem for months- then COVID19 hit’
For months, officials had been warning of a looming shortage in the supply of a gas used in the sterilization of medical equipment (Ethylene Oxide). That the system had now taken another hit and was stressed due to COVID19.

One of the most adopted sterilization processes uses ethylene oxide (EO), a highly reactive, toxic and flammable gas capable of sterilizing at ambient temperature, preserving those medical devices which cannot be exposed to moisture or high temperatures — like the ones made of polymers, plastics or those containing electronic components.

The EO sterilization is assumed to play an important role in the battle against COVID-19, but, due to its intrinsic hazardous nature and carcinogenic effect on human beings, very high attention must be paid on possible residual levels
This position is supported by the Centres for Disease Control and Prevention (CDC) which states, “Ethylene oxide is not recommended as a crisis strategy for cleaning filtering facepiece respirators as it may be harmful to the wearer.”

In this scenario, it becomes even more critical to rely on efficient and sensitive testing methods to ensure no residual EO is present on PPE and medical devices in general.

Ethylene Oxide is absorbed by many materials, for this reason, following sterilization the item must undergo aeration to remove any residual. Guidelines have been promoted regarding allowable EO limits for devices that depend on how the device is used, how often, and how long in order to pose a minimal risk to patients in normal product use

Additionally, during the EO sterilization process, it is also possible the formation of 2-chloroethanol (or ethylene chlorohydrin, ECH)2, which is classified as a hazardous substance very toxic by inhalation and skin absorption.
Ethylene Oxide is used for various medical devices including PCR tests to insert deeply into peoples nasal cavaties

Please go to the link in the image above which takes you to my Rumble video for more information on this serious subject.

QUESTIONS AND ANSWERS ON MEDSAFE WEBSITE- https://www.medsafe.govt.nz/COVID-19/q-and-a-vaccine-safety.asp

Should I be getting a COVID-19 vaccine while I am pregnant?
Currently, the Comirnaty (Pfizer) vaccine is the only COVID-19 vaccine available in New Zealand. There is limited data with the use of Comirnaty in pregnant women. Animal studies have not indicated direct or indirect harmful effects in pregnancy, development of the fetus or the newborn (NOTE: DOES NOT DOCUMENT HUMAN STUDIES)

What adverse effects (or events) after vaccination are doctors, nurses, DHB staff, pharmacists required to report to the Centre for Adverse Reactions Monitoring (CARM)?
There is no legal requirement for healthcare professionals to report adverse events following immunisation (AEFIs). However, we encourage healthcare professionals to report all AEFIs. Consumers can also report any reactions they experience to medicines and vaccines.
(NOTE: NO LEGAL REQUIREMENTS TO REPORT ADVERSE EFFECTS)

Are adverse events listed by the vaccine manufacturer in the package inserts and data sheets required to be reported to CARM?
There is no legal requirement to report adverse events. However, we encourage reporting of adverse events listed in the package inserts as well as any event that may be related to vaccination. ( NOTE: NO LEGAL REQUIREMENT )

If a patient has previously had an adverse event to a vaccine, can they receive a COVID-19 vaccine? (NOTE: AGAIN NO DIRECT ANSWER OF YES OR NO).

If a patient has previously had an adverse event to a vaccine, can they receive a COVID-19 vaccine?
Healthcare professionals should refer to the data sheet for information on contraindications to specific vaccines. These are published on our website.
(NOTE : AGAIN DOES NOT ANSWER YES OR NO )

Are the vaccines dangerous for people with previous COVID-19 infection?
The Cominarty clinical trials included people with previous COVID-19 infection. There are no known safety issues for people with previous infection. (NOTE: DOES NOT GIVE ANSWER YES OR NO)

Are the vaccines safe for children?
The Comirnaty vaccine is indicated for use in individuals aged 12 years and older. Clinical trials to assess safety and efficacy in children are ongoing. (NOTE: AGAIN NO YES OR NO ANSWER.. BUT TRIALS ARE STILL ONGOING… AS ARE THE HUMAN EXPERIMENTS ON OUR CHILDREN)

Are the vaccines safe for people with immunodeficiency or autoimmune conditions?
Refer to the vaccine’s Data Sheet or Consumer Medicine Information (CMI). (NOTE: STILL NO..YES OR NO ANSWERS)

What studies have Medsafe done to ensure the vaccine is safe for general use?
Medsafe does not conduct studies. Medsafe reviews the data submitted by the pharmaceutical company, including clinical trial data. (NOTE:- THEY DO NOT DO THEIR OWN TRIALS… NOTHING IS TRANSPARANT)

What is an acceptable number of side effects?
We encourage healthcare professionals and consumers to report any suspected side effect to a COVID-19 vaccine. For this reason, and because so many people will be receiving a vaccine, we expect many side effects to be reported.
Receiving large numbers of reports also indicates that the reporting system is working and easy to use.
Note that the cause of death is investigated and determined by the coroner, not by CARM or Medsafe. See the Coronial Services website (NOTE: DO NOT GIVE AN ANSWER AS TO ACCEPTABLE NUMBER OF SIDE EFFECTS..HOWEVER THEY WILL SEE AND THERE HAVE BEEN MANY MORE SERIOUS SIDE EFFECTS AND MORTALITIES)
ALSO PLEASE NOTE 5 -6 YEARS BACKLOG WITH INVESTIGATIONS IN CORONERIAL SERVICES.