REFERENCE TO:- https://voicesforfreedom.co.nz/blog/post/midwives-challenge-legality-vaccination-order

New Zealand Midwives are challenging the government legality of the vax order.
Voices for Freedom are doing are wonderful job. Tahnk you.
A big thank you to those wonderful midwives too for having the courage to make NZ Government accountable for their insanity, demands on immunizations. (Human Experiments) T

27 October 2021, media release…..Midwives Challenging Legality of Vaccination Order…
Late on Friday 22 October 2021, the Minister of COVID-19 Response issued an order which amended the COVID-19 Public Health Response (Vaccinations) Order 2021. That order was purportedly made under the COVID-19 Public Health Response Act 2020. It now specifies that, unless midwives submit to receiving a COVID-19 vaccination by 15 November 2021, they will lose their livelihoods and their vocation.

The order now applies to most workers in the health and disability sector, as well as prisons, schools and early childhood services.

The New Zealand Midwives’ Collective is a group of midwives from around New Zealand who have come together to oppose mandatory vaccination and uphold the right to informed choice and consent. On Monday a small group of midwives filed an application on behalf of the Collective, asking the High Court to declare the vaccination order invalid.

The basis for this challenge is that midwives, like all New Zealanders, have a right guaranteed under the New Zealand Bill of Rights Act 1990 to refuse medical treatment that they do not want, whether or not anyone else agrees with their reasons for doing so. It is about the personal autonomy that we all enjoy over our bodies. If the Government wants to limit that right, it cannot do that in a regulation made under the authority of a general provision in a statute. On at least two occasions this year alone, the Supreme Court has held that “Parliament cannot abridge fundamental rights and freedoms by general or ambiguous words”. That is what has been done here and it is an affront to New Zealand’s constitutional norms.

The New Zealand Midwives Collective strongly opposes any restrictions being placed upon informed consent – a fundamental principle of midwifery in our country. They believe this is detrimental to the profession and a dangerous precedent that will adversely impact the rights of birthing families. Since the Cartwright Inquiry, it is a line that has not been crossed in health care and has been enshrined in law by the Code of Health and Disability Services Consumers’ Rights.

Informed consent, by definition, must acknowledge not only the benefits, but also any risks or alternatives. By definition, it also must be free from the threat of being denied the right to work as a midwife. The Collective says that there is an opportunity to open a solution-based paradigm, investigating legitimate alternatives and controls that have

been used successfully internationally. They do not agree that vaccination is the only answer.

The Collective understands that between 200 and 300 New Zealand midwives will decline the COVID-19 vaccination. That accounts for between 8 and 10% of all practicing midwives. If the order is not struck down, these midwives will be required to stop work on 15 November 2021. The Collective says:

“Our maternity system is already desperately short of midwives but the Government has continued to ignore our pleas to make urgent changes. There are already significant midwifery roster gaps within the DHBs. The decision to mandate this COVID-19 vaccine and the subsequent reduction in hospital midwife numbers will further increase the current workforce pressure for employed midwives and make it unsafe for the mothers and families for whom they care.”

It has been suggested that, if midwives who are Lead Maternity Carers (LMC) are unable to practice, the DHBs as the providers of last resort will have to ensure that maternity services continue to be provided safely to expectant mothers who can no longer access an LMC. The Collective questions whether there is a realistic contingency plan to cope with this shortfall. The irony is that the healthcare outcomes for mothers and babies which result from the Vaccination Order may be worse than those from which it is intended to shield New Zealanders.

The Collective says:-
“We are standing up to protect the rights of women. Our profession will always draw a line when it comes to informed consent and bodily autonomy. This is a not just a midwifery issue, this is a human issue, a feminist issue and a civil rights issue. All birthing women have the right to have bodily autonomy respected and midwives are the safeguards of that. It is a grossly hypocritical demand from our government, and our professional and statutory bodies, to expect us to surrender this right. Midwives are the guardians of this right for women around pregnancy, birth and postpartum. We are midwives, supporting midwives to have the same rights as the women for whom we care.”

This statement has been authorised for release by the New Zealand Midwives’ Collective, represented by the applicants in CIV 2021-485-584 F v Minister for COVID-19 Response.

For further details, please contact Christopher Griggs on (04) 914 1053

These are the primary principles of the Helsinki Declaration:-
The basic principles include respect for individuals, the right to make informed decisions, recognition of vulnerable groups, and more. The Declaration of Helsinki has been revised six times, in 1975, 1983, 1989, 1996, 2000, and 2008.

The four basic principles of research are classified as autonomy, beneficence, non-maleficence, and justice.

THE PREAMBLE: The World Medical Association (WMA) has developed the Declaration of Helsinki as a statement of ethical principles for medical research involving human subjects, including research on identifiable human material and data.

The Declaration of Helsinki is consistent with the mandate of the WMA, the Declaration is addressed primarily to physicians. The WMA encourages others who are involved in medical research involving human subjects to adopt these principles.

GENERAL PRINCIPLES: -The Declaration of Geneva of the WMA binds the physician with the words, “The health of my patient will be my first consideration,” and the International Code of Medical Ethics declares that, “A physician shall act in the patient’s best interest when providing medical care.”
It is the duty of the physician to promote and safeguard the health, well-being and rights of patients, including those who are involved in medical research. The physician’s knowledge and conscience are dedicated to the fulfilment of this duty.

Medical progress is based on research that ultimately must include studies involving human subjects.
The primary purpose of medical research involving human subjects is to understand the causes, development and effects of diseases and improve preventive, diagnostic and therapeutic interventions (methods, procedures and treatments). Even the best proven interventions must be evaluated continually through research for their safety, effectiveness, efficiency, accessibility and quality.

Medical research is subject to ethical standards that promote and ensure respect for all human subjects and protect their health and rights. While the primary purpose of medical research is to generate new knowledge, this goal can never take precedence over the rights and interests of individual research subjects.
It is the duty of physicians who are involved in medical research to protect the life, health, dignity, integrity, right to self-determination, privacy, and confidentiality of personal information of research subjects. The responsibility for the protection of research subjects must always rest with the physician or other health care professionals and never with the research subjects, even though they have given consent.

Physicians must consider the ethical, legal and regulatory norms and standards for research involving human subjects in their own countries as well as applicable international norms and standards. No national or international ethical, legal or regulatory requirement should reduce or eliminate any of the protections for research subjects set forth in this Declaration.
Medical research should be conducted in a manner that minimises possible harm to the environment.

Medical research involving human subjects must be conducted only by individuals with the appropriate ethics and scientific education, training and qualifications. Research on patients or healthy volunteers requires the supervision of a competent and appropriately qualified physician or other health care professional.
Groups that are underrepresented in medical research should be provided appropriate access to participation in research.

Physicians who combine medical research with medical care should involve their patients in research only to the extent that this is justified by its potential preventive, diagnostic or therapeutic value and if the physician has good reason to believe that participation in the research study will not adversely affect the health of the patients who serve as research subjects
Appropriate compensation and treatment for subjects who are harmed as a result of participating in research must be ensured.

RISKS, BENEFITS AND BURDENS:- In medical practice and in medical research, most interventions involve risks and burdens. Medical research involving human subjects may only be conducted if the importance of the objective outweighs the risks and burdens to the research subjects.
All medical research involving human subjects must be preceded by careful assessment of predictable risks and burdens to the individuals and groups involved in the research in comparison with foreseeable benefits to them and to other individuals or groups affected by the condition under investigation.

Measures to minimise the risks must be implemented. The risks must be continuously monitored, assessed and documented by the researcher.
Physicians may not be involved in a research study involving human subjects unless they are confident that the risks have been adequately assessed and can be satisfactorily managed.
When the risks are found to outweigh the potential benefits or when there is conclusive proof of definitive outcomes, physicians must assess whether to continue, modify or immediately stop the study.

VUNERABLE GROUPS AND INDIVIDUALS:- Some groups and individuals are particularly vulnerable and may have an increased likelihood of being wronged or of incurring additional harm. All vulnerable groups and individuals should receive specifically considered protection.
Medical research with a vulnerable group is only justified if the research is responsive to the health needs or priorities of this group and the research cannot be carried out in a non-vulnerable group. In addition, this group should stand to benefit from the knowledge, practices or interventions that result from the research.

SCIENTIFIC REQUIREMENTS AND RESEARCH PROTOCOLS: – Medical research involving human subjects must conform to generally accepted scientific principles, be based on a thorough knowledge of the scientific literature, other relevant sources of information, and adequate laboratory and, as appropriate, animal experimentation. The welfare of animals used for research must be respected.
The design and performance of each research study involving human subjects must be clearly described and justified in a research protocol.
The protocol should contain a statement of the ethical considerations involved and should indicate how the principles in this Declaration have been addressed. The protocol should include information regarding funding, sponsors, institutional affiliations, potential conflicts of interest, incentives for subjects and information regarding provisions for treating and/or compensating subjects who are harmed as a consequence of participation in the research study.

In clinical trials, the protocol must also describe appropriate arrangements for post-trial provisions.
RESEARCH ETHIC COMMITTEE’S:- The research protocol must be submitted for consideration, comment, guidance and approval to the concerned research ethics committee before the study begins. This committee must be transparent in its functioning, must be independent of the researcher, the sponsor and any other undue influence and must be duly qualified. It must take into consideration the laws and regulations of the country or countries in which the research is to be performed as well as applicable international norms and standards but these must not be allowed to reduce or eliminate any of the protections for research subjects set forth in this Declaration.

The committee must have the right to monitor ongoing studies. The researcher must provide monitoring information to the committee, especially information about any serious adverse events. No amendment to the protocol may be made without consideration and approval by the committee. After the end of the study, the researchers must submit a final report to the committee containing a summary of the study’s findings and conclusions.

PRIVACY AND CONFIDENTIALITY:- Every precaution must be taken to protect the privacy of research subjects and the confidentiality of their personal information.
INFORMED CONSENT: Participation by individuals capable of giving informed consent as subjects in medical research must be voluntary. Although it may be appropriate to consult family members or community leaders, no individual capable of giving informed consent may be enrolled in a research study unless he or she freely agrees.

In medical research involving human subjects capable of giving informed consent, each potential subject must be adequately informed of the aims, methods, sources of funding, any possible conflicts of interest, institutional affiliations of the researcher, the anticipated benefits and potential risks of the study and the discomfort it may entail, post-study provisions and any other relevant aspects of the study. The potential subject must be informed of the right to refuse to participate in the study or to withdraw consent to participate at any time without reprisal. Special attention should be given to the specific information needs of individual potential subjects as well as to the methods used to deliver the information.

After ensuring that the potential subject has understood the information, the physician or another appropriately qualified individual must then seek the potential subject’s freely-given informed consent, preferably in writing. If the consent cannot be expressed in writing, the non-written consent must be formally documented and witnessed.

All medical research subjects should be given the option of being informed about the general outcome and results of the study.

When seeking informed consent for participation in a research study the physician must be particularly cautious if the potential subject is in a dependent relationship with the physician or may consent under duress. In such situations the informed consent must be sought by an appropriately qualified individual who is completely independent of this relationship.
For a potential research subject who is incapable of giving informed consent, the physician must seek informed consent from the legally authorised representative. These individuals must not be included in a research study that has no likelihood of benefit for them unless it is intended to promote the health of the group represented by the potential subject, the research cannot instead be performed with persons capable of providing informed consent, and the research entails only minimal risk and minimal burden.

When a potential research subject who is deemed incapable of giving informed consent is able to give assent to decisions about participation in research, the physician must seek that assent in addition to the consent of the legally authorised representative. The potential subject’s dissent should be respected.

Research involving subjects who are physically or mentally incapable of giving consent, for example, unconscious patients, may be done only if the physical or mental condition that prevents giving informed consent is a necessary characteristic of the research group. In such circumstances the physician must seek informed consent from the legally authorised representative. If no such representative is available and if the research cannot be delayed, the study may proceed without informed consent provided that the specific reasons for involving subjects with a condition that renders them unable to give informed consent have been stated in the research protocol and the study has been approved by a research ethics committee. Consent to remain in the research must be obtained as soon as possible from the subject or a legally authorised representative.

The physician must fully inform the patient which aspects of their care are related to the research. The refusal of a patient to participate in a study or the patient’s decision to withdraw from the study must never adversely affect the patient-physician relationship.

For medical research using identifiable human material or data, such as research on material or data contained in biobanks or similar repositories, physicians must seek informed consent for its collection, storage and/or reuse. There may be exceptional situations where consent would be impossible or impracticable to obtain for such research. In such situations the research may be done only after consideration and approval of a research ethics committee.

USE OF PLACEBO:- The benefits, risks, burdens and effectiveness of a new intervention must be tested against those of the best proven intervention(s), except in the following circumstances:
Where no proven intervention exists, the use of placebo, or no intervention, is acceptable; or
Where for compelling and scientifically sound methodological reasons the use of any intervention less effective than the best proven one, the use of placebo, or no intervention is necessary to determine the efficacy or safety of an intervention and the patients who receive any intervention less effective than the best proven one, placebo, or no intervention will not be subject to additional risks of serious or irreversible harm as a result of not receiving the best proven intervention. Extreme care must be taken to avoid abuse of this option

POST TRIAL PROVISIONS:- In advance of a clinical trial, sponsors, researchers and host country governments should make provisions for post-trial access for all participants who still need an intervention identified as beneficial in the trial. This information must also be disclosed to participants during the informed consent process.

RESEARCH REGISTRATION AND PUBLICATION AND DISSEMINATION OF RESULTS:- Every research study involving human subjects must be registered in a publicly accessible database before recruitment of the first subject.
Researchers, authors, sponsors, editors and publishers all have ethical obligations with regard to the publication and dissemination of the results of research. Researchers have a duty to make publicly available the results of their research on human subjects and are accountable for the completeness and accuracy of their reports. All parties should adhere to accepted guidelines for ethical reporting. Negative and inconclusive as well as positive results must be published or otherwise made publicly available. Sources of funding, institutional affiliations and conflicts of interest must be declared in the publication. Reports of research not in accordance with the principles of this Declaration should not be accepted for publication.

UNPROVEN INTERVENTIONS IN CLINICAL PRACTICE:- In the treatment of an individual patient, where proven interventions do not exist or other known interventions have been ineffective, the physician, after seeking expert advice, with informed consent from the patient or a legally authorised representative, may use an unproven intervention if in the physician’s judgement it offers hope of saving life, re-establishing health or alleviating suffering. This intervention should subsequently be made the object of research, designed to evaluate its safety and efficacy. In all cases, new information must be recorded and, where appropriate, made publicly available.

PRIVACY & CONFIDENTILITY: Every precaution must be taken to protect the privacy of research subjects and the confidentiality of their personal information.
INFORMED CONSENT: Participation by individuals capable of giving informed consent as subjects in medical research must be voluntary. Although it may be appropriate to consult family members or community leaders, no individual capable of giving informed consent may be enrolled in a research study unless he or she freely agrees.

In medical research involving human subjects capable of giving informed consent, each potential subject must be adequately informed of the aims, methods, sources of funding, any possible conflicts of interest, institutional affiliations of the researcher, the anticipated benefits and potential risks of the study and the discomfort it may entail, post-study provisions and any other relevant aspects of the study. The potential subject must be informed of the right to refuse to participate in the study or to withdraw consent to participate at any time without reprisal. Special attention should be given to the specific information needs of individual potential subjects as well as to the methods used to deliver the information.
After ensuring that the potential subject has understood the information, the physician or another appropriately qualified individual must then seek the potential subject’s freely-given informed consent, preferably in writing. If the consent cannot be expressed in writing, the non-written consent must be formally documented and witnessed.
All medical research subjects should be given the option of being informed about the general outcome and results of the study.

When seeking informed consent for participation in a research study the physician must be particularly cautious if the potential subject is in a dependent relationship with the physician or may consent under duress. In such situations the informed consent must be sought by an appropriately qualified individual who is completely independent of this relationship.
For a potential research subject who is incapable of giving informed consent, the physician must seek informed consent from the legally authorised representative. These individuals must not be included in a research study that has no likelihood of benefit for them unless it is intended to promote the health of the group represented by the potential subject, the research cannot instead be performed with persons capable of providing informed consent, and the research entails only minimal risk and minimal burden. When a potential research subject who is deemed incapable of giving informed consent is able to give assent to decisions about participation in research, the physician must seek that assent in addition to the consent of the legally authorised representative. The potential subject’s dissent should be respected.

Research involving subjects who are physically or mentally incapable of giving consent, for example, unconscious patients, may be done only if the physical or mental condition that prevents giving informed consent is a necessary characteristic of the research group. In such circumstances the physician must seek informed consent from the legally authorised representative. If no such representative is available and if the research cannot be delayed, the study may proceed without informed consent provided that the specific reasons for involving subjects with a condition that renders them unable to give informed consent have been stated in the research protocol and the study has been approved by a research ethics committee. Consent to remain in the research must be obtained as soon as possible from the subject or a legally authorised representative.

The physician must fully inform the patient which aspects of their care are related to the research. The refusal of a patient to participate in a study or the patient’s decision to withdraw from the study must never adversely affect the patient-physician relationship.
For medical research using identifiable human material or data, such as research on material or data contained in biobanks or similar repositories, physicians must seek informed consent for its collection, storage and/or reuse. There may be exceptional situations where consent would be impossible or impracticable to obtain for such research. In such situations the research may be done only after consideration and approval of a research ethics committee.

(9TH July 2018)
Clinical Study, Ethics, Ethics Committee, Helsinki, Human Subjects, Medical Research, Patient Autonomy, Placebo, Post-Trial Access, Principle, Publication, Register, Review Committee, Risk Assessment, Subject Protection, Vulnerable Populations..WMA Declaration of Cordoba on Patient-Physician Relationship
https://pubmed.ncbi.nlm.nih.gov/24141714/

WMA Declaration of Helsinki – Ethical Principles for Medical Research Involving Human Subjects

Fonterra is investing in la-grown artificial meat. Fonterra is investing in Montif ingredients, a Boston biotech start-up that uses genetic engineering and cultured ingredients to ‘make foods that are more sustainable’. Once again be alerted to that word ‘sustainable’. UN Agenda 2030 and its 17 Sustainable Development Goals and also the Great Reset.
Beyond Meats CEO says fake meat is good for farmers, so who is behind ‘Beyond Meats? Non other than Bill Gates, he has invested in a number of start-up’s relating to fake foods, fake meats. Plant based food is all part of the tech revolution, the ‘Great Reset’ and ‘UN Agenda 2030’ (Climate Alarmism)
It has been reported that by 2040 the alternative to real meat could make $240 billion in revenue globally.

I personally believe that the global fake meat industry will have a big impact on farmers, causing a disruption in beef production, as if its not bad enough already with this targeting of farmers with stricter regulations and also targeting them to significantly reduce livestock numbers.

Global Multistakeholder Capitalist wealthy Corporations are jumping on the gravy train when it comes to climate alarmism. Philanthropists like Bill Gates has invested in several start-up in the fake meat, fake food industry.

COVID-19 has spiked the increase of fake meats in supermarket refrigerators. In US grocery stores sales of fake meat has increased 264%.

The farmers in New Zealand are about to have another ‘Groundswell’ protest nationwide, the second one this year. Thousands of farmers in New Zealand had descended on dozens of towns and cities across the nation. They were protesting, demanding the government loosen its environmental policies, regulations which they are finding very difficult to deal with.

Farmers are not climate villains. The IPCC methane measurements are questionable, biogenic methane has been stable or has reduced each year in New Zealand since 2001. One must surely question is this a global scamdemic aligning itself with the plandemic. WHo actually understands the wellbeing indicator modelling and every other modelling these so called scientists and researchers use, which is called evidence based. Predictabilities, assumptions, data in and data out?? After all the government fund the researchers in these universities to provide them with the evidence to introduce policies and regulations that effect New Zealanders.

So, when it comes to fake meat, should we question is it a healthy replacement for real meat, or can it cause disease?

NOTE” PLEASE GO TO THE LINK ABOVE TO VIEW MY RMBLE VIDEO FOR MORE INFORMATION ON THIS TOPIC.

AN INTERESTING ARTICLE AUTHOURED BY: Brian Aiken November 16, 2020

Last year, Prime Minister Jacinda Ardern was a guest speaker at a private gathering in New York hosted by Bill & Melinda Gates.
She told the audience that New Zealand took the lead under her control and incorporated UN Agenda 2030 into our legal and regulatory framework.
“… My government is doing something that many other countries have never tried. We will incorporate the principles of the 2030 Agenda into domestic policymaking and promote system-level action. I want … I believe that the change in approach adopted in New Zealand is needed on a global scale … “
The event was arranged by the goalkeeper, an organization founded by the Gates Foundation in 2017 to accelerate progress towards the 17 Sustainable Development Goals of the United Nations Agenda 2030.

Melinda Gates told the audience in an ardent introduction to Jacinda Ardern that the Prime Minister “announced an international human rights program that promises New Zealand to lead, among other things, gender equality and the empowerment of women and girls.” It was.
She described our Prime Minister as “a true international leader who understands that the future of the world depends on eliminating inequality.”
It’s a shame that Jacinda Ardern wasn’t very positive about New Zealanders when he decided to follow the path of this experimental Agenda 2030. Most kiwis will not be completely aware that we have not only adopted UN doctrine, but are also world leaders in gender equality and empowerment of women and girls.

The Government of Ardern does not hide the fact that it is working to implement the United Nations Sustainable Development Goals, but it is open and transparent on the agenda that underpins those goals and the policy implications of “eliminating inequality.” There is no doubt that it is not.
Agenda 2030, not by name, was featured in the 2017 Confidence and Cooperation Agreement between Labour and Greens. Instead, both parties have committed to the 17 Sustainable Development Goals that underpin Agenda 2030.

“The Greens support a transformative government that implements the United Nations’ 17 Sustainable Development Goals. During this parliamentary term, the Greens set many priorities to promote the implementation of the Sustainable Development Goals. The Labour Party-led government will share and support these priorities. “
And that’s the way the Labour-led government has followed the country in the last three years.
This made Jacinda Ardern a child of the poster for Agenda 2030, the United Nations blueprint for modern socialism, but New Zealanders found that we were used as guinea pigs in international socialist experiments. Almost unaware.

In a speech at the 2018 International Conference on Sustainable Development in New York, the Prime Minister expressed his intention to lead the world by fully incorporating the Agenda 2030 Sustainable Development Goals (SDGs) into domestic affairs. It was. Other countries have done it before and have incorporated indicators like the SDGs into everything we do. “
She said the government no longer relies on traditional progress indicators such as “economic growth” and instead introduces new experimental indicators. “… establishing a whole new indicator of national achievement beyond growth … the standard of living framework we have created a tool called. It has the concept of sustainable intergenerational well-being. At the heart of various decision-making processes – policy advice, government spending, and long-term management of our assets.

“Our statistics department is working on an ambitious project called Indicators Aotearoa New Zealand, which aims to create a comprehensive set of indicators of New Zealanders’ current and future well-being. . Economical, cultural, social and environmental.
“These new tools will help us achieve and monitor the achievement of goals like the SDGs. The first test of this new approach will be early next year. At that time, we will use these new tools and new approaches. We provide the first budget. We call it the Happiness Budget and are not shy about investing in alternation of generations … “
Just before the 2019 “welfare” budget was announced, the Prime Minister explained to a New Zealand business audience what the new approach of the government would entail. “Economic growth is important and we continue to pursue, but that alone is the standard of living for New Zealanders … This year, the new well-being budget will allow us to lay a strong foundation for both our country and our people. I hope we can do it.

The mainstream media doesn’t seem to focus on Jacinda Ardern’s commitment to Agenda 2030, which is not surprising given the imbalance.
This week’s NZCPR guest commentator, Dr. Oliver Hartwich, Chief Executive Officer of the New Zealand Initiative, explains how difficult it is to speak openly to the government, especially in this country.

“Our small population fosters social adaptability that makes it difficult to speak our hearts. We cannot afford to burn the bridge because of the two gaps.
“Most of us no longer doubt whether it is based on reality, and anyone who does so is called non-patriotic and trivial, so risk falling apart. Please let me do it anyway. “
Dr. Hartwitch is particularly critical of housing-related policy failures. As he says, if there’s one thing New Zealand doesn’t lack, it’s space to build a house. Still, the high cost of the New Zealand section, combined with excessive bureaucratic planning and excessive building regulations, has led to the “most expensive” housing market in developed countries.
The lack of affordable housing has been such a scandal for many years, and successive governments have prioritized fixing it. However, it is of little use, so the ideological framework that caused the problem in the first place is well established.

The housing crisis originated in Agenda 21 of the United Nations, the predecessor of 2030, and has had a major impact on New Zealand’s private property rights for over 20 years. Designed to prevent “urban sprawl,” “smart growth” policies are being imposed by council planners above and below the country, creating a serious shortage of residential land. The impact is clear – higher section prices contributing to the current home affordability crisis.

Agenda 21 was founded by the United Nations in 1992, dating back to the first Earth Summit in Sweden in 1972. Based on the idea that humans are destroying the earth, we are trying to control our lives with sensible sounds. Reaching a “Sustainable Development” Policy Mechanism – Meet the needs of current generations without compromising the needs of future generations.
When the United Nations updated Agenda 21 to Agenda 2030 in 2015, they highlighted 17 Sustainable Development Goals to manage every aspect of our lives. From the end of poverty to the intensification of cities and the elimination of inequality, the United Nations has planned it all.

The following summary of Agenda 2030 goals from the United Nations website does not justify the complexity of the proposed restrictions. Learn more about.
– Goal 1. End all forms of poverty
– Goal 2. End hunger and promote sustainable agriculture
– Goal 3. Ensuring a healthy life and promoting well-being for all ages
– Goal 4. Ensuring comprehensive, equitable and quality education
– Goal 5. Achieve gender equality and empower all women and girls
– Goal 6. Ensure sustainable management of water and sanitation
– Goal 7. Ensuring access to sustainable energy
– Goal 8. Promote sustainable economic growth and decent work for all
– Goal 9. Promote comprehensive and sustainable industrialization
– Goal 10. Reduce national and domestic inequality
– Goal 11. Make cities and human settlements sustainable
– Goal 12. Ensure sustainable consumption and production patterns
– Goal 13. Take urgent action to combat climate change
– Goal 14. Sustainable use of the ocean
– Goal 15. Promote sustainable use of terrestrial ecosystems and stop biodiversity loss
– Goal 16. Promote inclusive societies and institutions for sustainable development
– Goal 17. Strengthen global partnerships for sustainable development

The UN concept was big and bold. They wanted a change in which every sector of society needed to mobilize 10 years of action. “To secure greater leadership, more resources … the necessary transitions to governments, cities, local governments … and include youth, civil society, the media, the private sector, trade unions, academia and other stakeholders. People’s actions create an unstoppable movement that drives the necessary changes.

At the heart of Agenda 2030, it is the “climate emergency” that justifies the need for “urgent” action. It is used to justify more regulation and control, claiming that humanity is destroying the planet. As a result, wildfires, droughts, floods and storms are all advertised as “evidence” that the global warming Armageddon is imminent. And it can only be avoided if countries take action to achieve UN goals, such as the redistribution of wealth. Poor countries.
In fact, this is the new face of socialism. The first is Agenda 21. Currently it is Agenda 2030. Next is “Agenda 2050”. For a new era socialist like Jacinda Ardern, “equality” is by no means equal enough, so it never stops.

Old school socialism fought the working class against the ruling class, but under the fundamental premise that exploiting the poor makes the rich richer, socialism is now in the struggle for equality. I changed my appearance. The underlying premise today is that it is fair to take from those who have it and give it to those who do not.
It has evolved into an obsession with equality of wealth, rather than all the most important principles of equal opportunity.
It’s a matter of dividing the country now. But the difference between New Zealand and most other counties is that there is no public debate here. We are transforming into a socialist country, but there is no full disclosure by the politicians driving this fundamental change.

There was no effective media investigation into these developments, nor was there an effective scrutiny from opposition politicians.
As a result, as Dr. Hartwitch points out, it is becoming increasingly difficult to discuss these issues freely. Especially now, the media is very openly biased to the left. In fact, it is our society that the Fourth Estate, once a guardian of truth, is now part of the problem and that much of the media has crossed the line from critical analysis and fact reporting to politics. It’s a tragedy for me. Advocacy.

Given the current lack of a balanced view, access to information has never been easier, but access to the truth has certainly never been more difficult. It’s ironic.
Behind the smile lies the most radical socialist government in our history, with the Prime Minister intending to incorporate the purpose of the world’s most socialist organizations into our policy and legislative framework. There is no doubt that it is.

To fight back, you need to start calling out what socialism is, but to call it out, you first need to lift the veil to find out what’s going on.
Next, we need to decide whether we want to be a socialist society that gives from those who achieve it to those who don’t, or whether New Zealand aims to be an opportunity society where everyone has a chance to improve. Myself and my family.

In other words, should New Zealand follow the path to socialism under the United Nations Agenda 2030, or should we respect people’s individualism and freedom and ensure that they have the opportunity to move forward? ??

In the latter case, by the time of the next election, we have a lot to stand up and speak together!

New Zealand’s Road to UN Agenda 2030
Source link New Zealand’s Road to UN Agenda 2030
LINK: https://eminetra.co.nz/new-zealands-road-to-un-agenda-2030/80172/