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Critics highlight certain phrases and concepts that raise red flags, such as “stakeholder capitalism,” which suggests a shift towards a more collectivist economic model. They argue that this could pave the way for increased Government control and diminish the role of free markets.
Moreover, sceptics point to the involvement of influential figures like Bill Gates, who has advocated for population control measures in the past.
This connection fuels suspicions that the Great Reset may be a vehicle for implementing population control strategies under the guise of sustainability.
As critical thinkers, it is essential to engage in thorough research and examine multiple perspectives to form an informed opinion.
While the Great Reset claims to carry the potential for positive change, this could not be further from the truth and it is crucial to oppose, and if needed monitor, its implementation and ensure transparency and accountability.
By staying vigilant and demanding open dialogue, we can actively participate in shaping our collective future and ensure that it aligns with our values and aspirations.
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To understand Gates’ philanthropic endeavours, it is essential to delve into the work of the Bill & Melinda Gates Foundation. The foundation focuses on addressing some of the world’s most pressing challenges, such as poverty, infectious diseases, and education.
Through partnerships with governments, NGOs, and other philanthropic organizations, the foundation aims to improve the quality of life for millions of people worldwide.
One of the primary areas of focus for the Gates Foundation is global health. Gates has been a strong advocate for vaccination campaigns, particularly in developing countries, aiming to combat diseases like polio, malaria, and HIV/AIDS.
However, these efforts are not driven by benevolence but rather serve as a means to control population growth and make huge profits.
Gates’ financial investments have also come under scrutiny. Some argue that his involvement in industries such as pharmaceuticals and genetically modified crops indicates a hidden agenda to profit from global health crises or control the food supply.
Gates’ financial investments have sparked speculation and raised concerns. One area of scrutiny lies in his involvement in the pharmaceutical industry. Critics point to his significant investments in pharmaceutical companies, suggesting that his philanthropic endeavours in the field of public health may be driven by profit motives rather than solely altruistic intentions.
They argue that by promoting vaccines and other medical interventions, Gates stands to benefit financially from the widespread adoption of these products.
Additionally, Gates’ investments in genetically modified (GM) crops have fueled suspicions regarding his control over the global food supply. His support for GM technology is part of a broader agenda to monopolize agriculture and exert influence over the world’s food production systems.
This control would grant Gates immense power and potentially enable him to manipulate food availability and prices to serve his own interests.
Gates of course denies this and has publicly stated that his investments align with his goal of addressing pressing global challenges, including improving health outcomes and enhancing food security. He asserts that his financial involvement allows him to leverage resources and expertise to make a meaningful impact in these areas.
But as critical thinkers, it is vital to engage in objective analysis, consider multiple perspectives, and demand transparency and accountability from all individuals and organizations involved in shaping our world.
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To understand the role of vaccines, it is crucial to examine their scientific foundation. Vaccines allegedly work by stimulating the immune system to recognize and respond to specific pathogens, preparing the body to defend itself against future infections.
Prior to the Emergency Use Authorization (EUA) of the Covid-19 vaccines, the development and approval process for vaccines typically followed a rigorous timeline involving several stages of research, clinical trials, and regulatory scrutiny.
It is true that the average timeline for vaccine development, from initial discovery to final approval, historically took around 8 to 10 years. This prolonged timeline allowed for comprehensive and extensive testing to assess the safety, efficacy, and potential long-term effects of the vaccine candidates.
The traditional vaccine development process involved various phases, including preclinical testing in the laboratory and on animals, followed by three distinct phases of clinical trials involving human subjects.
Phase 1 trials primarily focused on assessing the vaccine’s safety and dosage levels in a small group of healthy volunteers.
Phase 2 trials expanded the study population to hundreds of individuals to evaluate the vaccine’s immunogenicity and further assess its safety profile.
Phase 3 trials, which are often the largest and most time-consuming phase, involved thousands to tens of thousands of participants.
These trials aimed to determine the vaccine’s efficacy in preventing the target disease while closely monitoring for any potential side effects.
During this phase, participants were divided into two groups, with one group receiving the vaccine and the other receiving a placebo or an alternative control measure. The researchers then compared the outcomes between the groups to evaluate the vaccine’s effectiveness.
Following the completion of clinical trials, vaccine developers would compile and submit extensive data to regulatory bodies, such as the US Food and Drug Administration (FDA) or the European Medicines Agency (EMA), for review and approval.
These regulatory agencies allegedly rigorously scrutinize the data, including the vaccine’s safety and efficacy profiles, manufacturing processes, and quality control measures, before granting approval for public use.
However, in the case of the alleged Covid-19 pandemic, the development and approval process for vaccines underwent an accelerated timeline of just a few months.
The Emergency Use Authorization (EUA) mechanism allowed vaccines to be made available for emergency use before the completion of the usual lengthy regulatory process that ensured vaccines were safe for use among humans.
The decision to do this was extremely questionable when we consider that Bill Gates has shares in the major Covid-19 vaccine companies and was also a major funder of medicine regulators through his foundation.
The Bill and Melinda Gates Foundation has been a significant contributor to global health initiatives, including vaccine research and development. The foundation has provided funding for various organizations involved in vaccine development and delivery, including the World Health Organization (WHO), the Coalition for Epidemic Preparedness Innovations (CEPI), and Gavi, the Vaccine Alliance.
Therefore, this conflict of interest stinks of corruption as Bill Gates could have threatened to withdraw his funding to medicine regulators if they failed to grant EUA of the Covid-19 injections he had shares in to increase his return on those shares.
In 2017, the UK Medicine Regulator, the MHRA, received a grant from the Bill & Melinda Gates Foundation worth £980,000 to facilitate a “collaboration” between the two entities.
Source
But according to a Freedom of Information request answered by the MHRA in May 2021, the Gates Foundation sent funds of over $3 million to the MHRA to support “a number of projects.”
Source
While this relationship might not have raised eyebrows under different circumstances, the fact that the Gates Foundation owns shares in companies developing Covid-19 vaccines authorized for emergency use in children by the MHRA raises questions about potential conflicts of interest.
In 2016, Moderna announced that the Bill & Melinda Gates Foundation had granted them $20 million to support their initial project, which involved the evaluation of antibody combinations in a preclinical setting and the conduct of a Phase 1 clinical trial for a potential mRNA injection.
Source
Moderna also revealed that the framework agreement between Moderna and the Gates Foundation could potentially result in total funding of up to $100 million for follow-on projects proposed and approved by the Gates Foundation through 2022.
As part of this agreement, Moderna is obliged to grant the Gates Foundation certain non-exclusive licenses.
The Bill & Melinda Gates Foundation also bought shares in Pfizer back in 2002 before “coincidentally” buying $55 million worth of shares in BioNTech in September 2019, just before the alleged Covid-19 pandemic struck.
The partnership between Pfizer and BioNTech has proven to be highly profitable, as their Covid-19 vaccine was among the first to receive emergency use authorizations worldwide.
This rapid approval and widespread distribution have resulted in a substantial increase in the stock prices of both companies.
Consequently, the Gates Foundation’s investments in these corporations have also grown in value, adding to the foundation’s already significant wealth.
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The real-world evidence surrounding Covid-19 vaccines strongly suggests that they contain harmful substances and serve as a covert means to control fertility and cause depopulation.
The allegations are supported by scientific evidence contained in published Government data.
Ovarian Cancer – Source
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Source
All of the above points to the potential for depopulation due to the horrific effects, discovered in the confidential Pfizer documents, that Covid-19 vaccination can have on the ovaries, fertility, pregnancy, and newborn babies.
However, further figures on the incredible amount of excess deaths all but confirm that Covid-19 vaccination is a recipe for a depopulation disaster.
As Governments around the world raced to coerce every man, woman and child they could to get the Covid-19 vaccine, they gave away an astounding $75 billion of taxes collected from your hard-earned money to Pfizer, a company with a dark history of offences and fines, for its experimental mRNA injection.
This massive investment was allegedly made in the name of public health, but real-world data strongly suggests otherwise. However, it should come as no surprise considering our health and well-being were left in the hands of a company that has caused significant harm to the public in the past.
The data provided to the Organisation for Economic Co-Operation and Development (OECD) and EuroMOMO by official Government departments points to a significant increase in excess deaths since the rollout of Covid-19 vaccines in the USA, Canada, New Zealand, Australia, the UK and half of Europe. (Source)
This surge in excess deaths raises concerns about the safety and efficacy of the vaccines, especially considering the drastic differences in excess deaths before and after the vaccine rollout.
Source
Data provided to EuroMOMO by 27 countries across Europe highlights a striking correlation between the European Medicine Agency’s (EMA) extension of the emergency use authorization for the Pfizer COVID-19 vaccine to children aged 12 to 15 and the subsequent increase in excess deaths among children across Europe. (Source)
Excess deaths among children aged 0 to 14 across 27 countries across Europe, including the UK, France, Spain, Italy and most of Germany, increased by 760% up to week 12 of 2023 following the European Medicines Agency extending the emergency use authorization of the Pfizer COVID-19 vaccine to children aged 12 to 15. (Source)
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Transparency in vaccine development, regulatory processes, and post-marketing surveillance is essential for building public trust and fostering informed decision-making.
It is also vital to respect individual autonomy and provide accurate information to empower individuals to make informed choices regarding their health and well-being.
Read more at: Expose-News.com
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