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  • Who Really Runs the World? Conspiracies, Hidden Agendas & the Plan for World Government
    May 22, 2013

    Andrew Gavin Marshall, New Dawn
    Waking Times

    So, who runs the world? It’s a question that people have struggled with since people began to struggle. It’s certainly a question with many interpretations, and incites answers of many varied perspectives.

    Often, it is relegated to the realm of “conspiracy theory,” in that, those who discuss this question or propose answers to it, are purveyors of a conspiratorial view of the world. However, it is my intention to discard the labels, which seek to disprove a position without actually proving anything to the contrary. One of these labels – “conspiracy theorist” – does just that: it’s very application to a particular perspective or viewpoint has the intention of “disproving without proof;” all that is needed is to simply apply the label.

    What I intend to do is analyse the social structure of the transnational ruling class, the international elite, who together run the world. This is not a conspiratorial opinion piece, but is an examination of the socially constructed elite class of people; what is the nature of power, how does it get used, and who holds it?

    A Historical Understanding of Power

    In answering the question “Who Runs the World?” we must understand what positions within society hold the most power, and thus, the answer becomes clear. If we simply understand this as heads of state, the answer will be flawed and inaccurate. We must examine the globe as a whole, and the power structures of the global political economy.



    The greatest position of power within the global capitalist system lies in the authority of money-creation: the central banking system. The central banking system, originating in 1694 in England, consists of an international network of central banks that are privately owned by wealthy shareholders and are granted governmental authority to print and issue a nation’s currency, and set interest rates, collecting revenue and making profit through the interest charged. Central banks give loans to both governments and industries, controlling both simultaneously. The ultimate centre of power in the central banking system is at the Bank for International Settlements (BIS), in Basle, Switzerland; which is the central bank to the world’s central banks, and is also a private bank owned by the world’s central banks.
    As Georgetown University history professor Carroll Quigley wrote:

    [T]he powers of financial capitalism had another far-reaching aim, nothing less than to create a world system of financial control in private hands able to dominate the political system of each country and the economy of the world as a whole. This system was to be controlled in a feudalist fashion by the central banks of the world acting in concert, by secret agreements arrived at in frequent private meetings and conferences. The apex of the system was to be the Bank for International Settlements in Basle, Switzerland, a private bank owned and controlled by the world’s central banks which were themselves private corporations.1

    The central banks, and thus the central banking system as a whole, is a privately owned system in which the major shareholders are powerful international banking houses. These international banking houses emerged in tandem with the evolution of the central banking system. The central banking system first emerged in London, and expanded across Europe with time. With that expansion, the European banking houses also rose and expanded across the continent.

    The French Revolution resulted with Napoleon coming to power, who granted the French bankers a central bank of France, which they privately controlled.2 It was also out of the French Revolution that one of the major banking houses of the world emerged, the Rothschilds. Emerging out of a European Jewish ghetto, the Rothschilds quickly rose to the forefront in banking, and established banking houses in London, Paris, Frankfurt, Vienna and Naples, allowing them to profit off of all sides in the Napoleonic wars.3

    As Carroll Quigley wrote in his monumental Tragedy and Hope, “The merchant bankers of London had already at hand in 1810-1850 the Stock Exchange, the Bank of England, and the London money market,” and that:

    In time they brought into their financial network the provincial banking centres, organised as commercial banks and savings banks, as well as insurance companies, to form all of these into a single financial system on an international scale which manipulated the quantity and flow of money so that they were able to influence, if not control, governments on one side and industries on the other.4

    At the same time, in the United States, we saw the emergence of a powerful group of bankers and industrialists, such as the Morgans, Astors, Vanderbilts, Rockefellers, and Carnegies, and they created massive industrial monopolies and oligopolies throughout the 19th century.5 These banking interests were very close to and allied with the powerful European banking houses.

    The European, and particularly the British elites of the time, were beginning to organise their power in an effort to properly exert their influence internationally. At this time, European empires were engaging in the Scramble for Africa, in which nearly the entire continent of Africa, save Ethiopia, was colonised and carved up by European nations. One notable imperialist was Cecil Rhodes who made his fortune from diamond and gold mining in Africa with financial support from the Rothschilds,6 and “at that time [had] the biggest concentration of financial capital in the world.”7

    Cecil Rhodes was also known for his radical views regarding America, particularly in that he would “talk with total seriousness of ‘the ultimate recovery of the United States of America as an integral part of the British Empire’.”8 Rhodes saw himself not simply as a moneymaker, but primarily as an “empire builder.”

    As Carroll Quigley explained, in 1891 three British elites met with the intent to create a secret society. The three men were Cecil Rhodes, William T. Stead, a prominent journalist of the day, and Reginald Baliol Brett, a “friend and confidant of Queen Victoria, and later to be the most influential adviser of King Edward VII and King George V.” Within this secret society, “real power was to be exercised by the leader, and a ‘Junta of Three.’ The leader was to be Rhodes, and the Junta was to be Stead, Brett, and Alfred Milner.”9

    The purpose of this secret society, which was later headed by Alfred Milner, was: “The extension of British rule throughout the world, the perfecting of a system of emigration from the United Kingdom and of colonisation by British subjects of all lands wherein the means of livelihood are attainable by energy, labour, and enterprise… [with] the ultimate recovery of the United States of America as an integral part of a British Empire.” [Emphasis added]10 Essentially, it outlined a British-led cosmopolitical world order, one global system of governance under British hegemony. Among key players within this group were the Rothschilds and other banking interests.11

    After the 1907 banking panic in the US, instigated by JP Morgan, pressure was placed upon the American political establishment to create a “stable” banking system. In 1910, a secret meeting of financiers was held on Jekyll Island, where they planned for the “creation of a National Reserve Association with fifteen major regions, controlled by a board of commercial bankers but empowered by the federal government to act like a central bank – creating money and lending reserves to private banks.”12

    It was largely Paul M. Warburg, a Wall Street investment banker, who “had come up with a design for a single central bank [in 1910]. He called it the United Reserve Bank. From this and his later service on the first Federal Reserve Board, Warburg has, with some justice, been called the father of the System.”13President Woodrow Wilson followed the plan almost exactly as outlined by the Wall Street financiers, and added to it the creation of a Federal Reserve Board in Washington, which the President would appoint.14

    Thus, true power in the world order was held by international banking houses, which privately owned the global central banking system, allowing them to control the credit of nations, and finance and control governments and industry.

    However, though the economic system was firmly in their control, allowing them to establish influence over finance, they needed to shape elite ideology accordingly. In effect, what was required was to socially construct a ruling class, internationally, which would serve their interests. To do this, these bankers set out to undertake a project of establishing think tanks to organise elites from politics, economics, academia, media, and the military into a generally cohesive and controllable ideology.

    Constructing a Ruling Class: Rise of the Think Tanks

    During World War I, a group of American scholars were tasked with briefing “Woodrow Wilson about options for the postwar world once the Kaiser and imperial Germany fell to defeat.” This group was called, “The Inquiry.” The group advised Wilson mostly through his trusted aide, Col. Edward M. House, who was Wilson’s “unofficial envoy to Europe during the period between the outbreak of World War I in 1914 and the intervention by the United States in 1917,” and was the prime driving force in the Wilson administration behind the establishment of the Federal Reserve System.15

    “The Inquiry” laid the foundations for the creation of the Council on Foreign Relations (CFR), the most powerful think tank in the US and, “The scholars of the Inquiry helped draw the borders of post World War I central Europe.” On May 30, 1919, a group of scholars and diplomats from Britain and the US met at the Hotel Majestic, where they “proposed a permanent Anglo-American Institute of International Affairs, with one branch in London, the other in New York.” When the scholars returned from Paris, they were met with open arms by New York lawyers and financiers, and together they formed the Council on Foreign Relations in 1921. The “British diplomats returning from Paris had made great headway in founding their Royal Institute of International Affairs.” The Anglo-American Institute envisioned in Paris, with two branches and combined membership was not feasible, so both the British and American branches retained national membership, however, they would cooperate closely with one another.16 They were referred to, and still are, as “Sister Institutes.”17

    The Milner Group, the secret society formed by Cecil Rhodes, “dominated the British delegation to the Peace Conference of 1919; it had a great deal to do with the formation and management of the League of Nations and of the system of mandates; it founded the Royal Institute of International Affairs in 1919 and still controls it.”18

    There were other groups founded in many countries representing the same interests of the secret Milner Group, and they came to be known as the Round Table Groups, preeminent among them were the Royal Institute of International Affairs (Chatham House), the Council on Foreign Relations in the United States, and parallel groups were set up in Canada, Australia, New Zealand, South Africa and India.19

    These were, in effect, the first international think tanks, which remain today, and are in their respective nations, among the top, if not the most prominent think tanks.

    In 2008, a major study was done by the University of Philadelphia’s International Relations Program – the Think Tanks and Civil Societies Program – which sought to analyse and examine the most powerful and influential think tanks in the world. While it is a useful resource to understanding the influence of think tanks, there is a flaw in its analysis. It failed to take into account the international origins of the Round Table Group think tanks, particularly the Council on Foreign Relations in the United States; Chatham House or the Royal Institute of International Affairs in London; the Canadian Institute of International Affairs, now renamed the Canadian International Council; and their respective sister organisations in India, South Africa, New Zealand and Australia. Further nations have since added to this group of related think tanks, including Germany, and a recently established European Council on Foreign Relations. The report, while putting focus on the international nature of think tanks, analysed these ones as separate institutions without being related or affiliated. This has, in effect, skewed the results of the study. However, it is still useful to examine.

    The top think tanks in the United States include the Council on Foreign Relations, (which was put at number 2, however, should be placed at the number 1 spot), the Brookings Institution, (which was inaccurately given the position of number one), the Carnegie Endowment for International Peace, RAND Corporation, Heritage Foundation, Woodrow Wilson International Centre for Scholars, the Center for Strategic and International Studies, and the American Enterprise Institute, among others.

    The top think tanks in the world, outside of the United States, are Chatham House (sitting at number one), the International Institute for Strategic Studies in the UK, the German Council on Foreign Relations, the French Institute of International Relations, the Adam Smith Institute in the UK, the Fraser Institute in Canada, the European Council on Foreign Relations, the International Crisis Group in Belgium, and the Canadian Institute of International Affairs.20

    In 1954, the Bilderberg Group was founded in the Netherlands. Every year since then the group holds a secretive meeting, drawing roughly 130 of the political-financial-military-academic-media elites from North America and Western Europe as “an informal network of influential people who could consult each other privately and confidentially.”21

    Regular participants include the CEOs or Chairmen of some of the largest corporations in the world, oil companies such as Royal Dutch Shell, British Petroleum, and Total SA, as well as various European monarchs, international bankers such as David Rockefeller, major politicians, presidents, prime ministers, and central bankers of the world.22 The Bilderberg Group acts as a “secretive global think-tank,” with an original intent “to link governments and economies in Europe and North America amid the Cold War.”23

    In 1970, David Rockefeller became Chairman of the Council on Foreign Relations, while also being Chairman and CEO of Chase Manhattan. In 1970, an academic who joined the Council on Foreign Relations in 1965 wrote a book called Between Two Ages: America’s Role in the Technetronic Era. The author, Zbigniew Brzezinski, called for the formation of “A Community of the Developed Nations,” consisting of Western Europe, the United States and Japan. Brzezinski wrote about how “the traditional sovereignty of nation states is becoming increasingly unglued as transnational forces such as multinational corporations, banks, and international organisations play a larger and larger role in shaping global politics.”

    So, in 1972, David Rockefeller and Brzezinski “presented the idea of a trilateral grouping at the annual Bilderberg meeting.” In July of 1972, seventeen powerful people met at David Rockefeller’s estate in New York to plan for the creation of another grouping. Also at the meeting was Brzezinski, McGeorge Bundy, the President of the Ford Foundation, (brother of William Bundy, editor of Foreign Affairs) and Bayless Manning, President of the Council on Foreign Relations.24 In 1973, these people formed the Trilateral Commission, which acted as a sister organisation to Bilderberg, linking the elites of Western Europe, North America, and Japan into a transnational ruling class.

    These think tanks have effectively socially constructed an ideologically cohesive ruling class in each nation and fostered the expansion of international ideological alignment among national elites, allowing for the development of a transnational ruling class sharing a dominant ideology.

    These same interests, controlled by the international banking houses, had to socially construct society itself. To do this, they created a massive network of tax-exempt foundations and non-profit organisations, which shaped civil society according to their designs. Among the most prominent of these are the Carnegie Corporation, the Ford Foundation, and the Rockefeller Foundation.

    The “Foundations” of Civil Society

    These foundations shaped civil society by financing research projects and initiatives into major social projects, creating both a dominant world-view for the elite classes, as well as managing the other classes.

    These foundations, since their establishment, played a large part in the funding and organising of the eugenics movement, which helped facilitate this racist, elitist ideology to having enormous growth and influence, ultimately culminating in the Nazi Holocaust. From then, the word “eugenics” had to be dropped from the ideology and philanthropy of elites, and was replaced with new forms of eugenics policies and concepts. Among them, genetics, population control and environmentalism.

    These foundations also funded seemingly progressive and alternative media sources in an effort to control the opposition, and manage the resistance to their world order, essentially making it ineffective and misguided.

    The Rockefeller Foundation was established in 1912, and immediately began giving money to eugenics research organisations.25 Eugenics was a pseudo-scientific and social science movement that emerged in the late 19th century, and gained significant traction in the first half of the 20th century. One of the founding ideologues of eugenics, Sir Francis Galton, an anthropologist and cousin to Charles Darwin, wrote that eugenics “is the study of all agencies under social control which can improve or impair the racial quality of future generations.”26 Ultimately, it was about the “sound” breeding of people and maintaining “purity” and “superiority” of the blood. It was an inherently racist ideology, which saw all non-white racial categories of people as inherently and naturally inferior, and sought to ground these racist theories in “science.”

    The vast wealth and fortunes of the major industrialists and bankers in the United States flowed heavily into the eugenics organisations, promoting and expanding this racist and elitist ideology. Money from the Harriman railroad fortune, with millions given by the Rockefeller and Carnegie family fortunes were subsequently “devoted to sterilisation of several hundred thousands of American ‘defectives’ annually, as a matter of eugenics.”27

    In the United States, 27 states passed eugenics based sterilisation laws of the “unfit,” which ultimately led to the sterilisation of over 60,000 people. Throughout the 1920s and 30s, the Carnegie and especially the Rockefeller Foundation, funded eugenics research in Germany, directly financing the Nazi scientists who perpetrated some of the greatest crimes of the Holocaust.28

    Following the Holocaust, the word “eugenics” was highly discredited. Thus, these elites who wanted to continue with the implementation of their racist and elitist ideology desperately needed a new name for it. In 1939, the Eugenics Records Office became known as the Genetics Record Office.29 However, tens of thousands of Americans continued to be sterilised throughout the 40s, 50s and 60s, the majority of which were women.30

    Edwin Black analysed how the pseudoscience of eugenics transformed into what we know as the science of genetics. In a 1943 edition of Eugenical News, an article titled “Eugenics After the War,” cited Charles Davenport, a major founder of eugenics, in his vision of “a new mankind of biological castes with master races in control and slave races serving them.”31

    A 1946 article in Eugenical News stated that, “Population, genetics, [and] psychology, are the three sciences to which the eugenicist must look for the factual material on which to build an acceptable philosophy of eugenics and to develop and defend practical eugenics proposals.” As Black explained, “the incremental effort to transform eugenics into human genetics forged an entire worldwide infrastructure,” with the founding of the Institute for Human Genetics in Copenhagen in 1938, led by Tage Kemp, a Rockefeller Foundation eugenicist, and was financed with money from the Rockefeller Foundation.32

    Today, much of civil society and major social projects are a product of these foundations, and align with various new forms of eugenics. The areas of population control and environmentalism are closely aligned and span a broad range of intellectual avenues. The major population control organisations emerged with funding from these various foundations, particularly the Rockefeller foundations and philanthropies.

    These organisations, such as the Rockefeller and Ford foundations, funded major civil society movements, such as the Civil Rights movement, in an effort to “create a wedge between social movement activists and their unpaid grassroots constituents, thereby facilitating professionalisation and institutionalisation within the movement,” ultimately facilitating a “narrowing and taming of the potential for broad dissent,” with an aim of limiting goals to “ameliorative rather than radical change.”33

    Two major organisations in the development of the environmental movement were the Conservation Foundation and Resources for the Future, which were founded and funded with money from the Rockefeller and Ford Foundations, and helped “launch an explicitly pro-corporate approach to resource conservation.”34 Even the World Wildlife Fund was founded in the early 1960s by the former president of the British Eugenics Society, and its first President was Prince Bernhard of the Netherlands, a founding member of the Bilderberg Group.

    While the environmental movement positions people as the major problem for the earth, relating humanity to a cancer, population control becomes a significant factor in proposing environmental solutions.

    In May of 2009, a secret meeting of billionaire philanthropists took place in which they sought to coordinate how to “address” the world’s environmental, social, and industrial threats. Each billionaire at the meeting was given 15 minutes to discuss their “preferred” cause, and then they deliberated to create an “umbrella” cause to harness all their interests. The end result was that the umbrella cause for which the billionaires would aim to “give to” was population control, which “would be tackled as a potentially disastrous environmental, social and industrial threat.” Among those present at the meeting were David Rockefeller, Jr., George Soros, Warren Buffet, Michael Bloomberg, Ted Turner, Bill Gates, and even Oprah Winfrey.35

    Conclusion

    At the top of the list of those who run the world, we have the major international banking houses, which control the global central banking system. From there, these dynastic banking families created an international network of think tanks, which socialised the ruling elites of each nation and the international community as a whole, into a cohesive transnational elite class. The foundations they established helped shape civil society both nationally and internationally, playing a major part in the funding – and thus coordinating and co-opting – of major social-political movements.

    An excellent example of one member of the top of the hierarchy of the global elite is David Rockefeller, patriarch of the Rockefeller family. Long serving as Chairman and CEO of Chase Manhattan bank, he revolutionised the notion of building a truly global bank. He was also Chairman of the Council on Foreign Relations, a founding member of Bilderberg and the Trilateral Commission, heavily involved in the family philanthropies, and sits atop a vast number of boards and foundations. Even Alan Greenspan, in a speech to the Council on Foreign Relations, said that David Rockefeller and the CFR have, “in many respects, formulated the foreign policy of this country.”36

    In another speech to the Council on Foreign Relations, then World Bank President James Wolfesohn, said in 2005, in honour of David Rockefeller’s 90th birthday, that, “the person who had perhaps the greatest influence on my life professionally in this country, and I’m very happy to say personally there afterwards, is David Rockefeller.” He then said, “In fact, it’s fair to say that there has been no other single family influence greater than the Rockefeller’s in the whole issue of globalisation and in the whole issue of addressing the questions which, in some ways, are still before us today. And for that David, we’re deeply grateful to you and for your own contribution in carrying these forward in the way that you did.”37

    David Rockefeller, himself, wrote, “For more than a century ideological extremists at either end of the political spectrum have seized upon well-publicised incidents such as my encounter with Castro to attack the Rockefeller family for the inordinate influence they claim we wield over American political and economic institutions. Some even believe we are part of a secret cabal working against the best interests of the United States, characterising my family and me as ‘internationalists’ and of conspiring with others around the world to build a more integrated global political and economic structure – one world, if you will. If that’s the charge, I stand guilty, and I am proud of it.”38



    About the Author

    ANDREW G. MARSHALL is a Research Associate with the Centre for Research on Globalization based out of Montreal, Canada (www.globalresearch.ca). He has written extensively on issues imperialism in the Middle East and Africa, the environment, Homeland Security, war, terrorism and the global economy. He is currently studying Global Political Economy and the History of the Middle East and Africa at Simon Fraser University (Canada).

    Footnotes:

    1. Carroll Quigley, Tragedy and Hope: A History of the World in Our Time, New York: Macmillan Company, 1966, 324

    2. Carroll Quigley, op.cit., 515; Robert Elgie and Helen Thompson, ed., The Politics of Central Banks, New York: Routledge, 1998, 97-98

    3. Sylvia Nasar, ‘Masters of the Universe’, The New York Times: January 23, 2000; ‘The Family That Bankrolled Europe’, BBC News: July 9, 1999, http://news.bbc.co.uk/1/hi/uk/389053.stm

    4. Carroll Quigley, op.cit., 51

    5. Howard Zinn, A People’s History of the United States, Harper Perennial: New York, 2003, 323

    6. Carroll Quigley, op.cit., 130

    7. Niall Ferguson, Empire: The Rise and Demise of the British World Order and the Lessons for Global Power, New York: Basic Books, 2004, 186

    8. Ibid, 190

    9. Carroll Quigley, The Anglo-American Establishment, GSG & Associates, 1981, 3

    10. Ibid, 33

    11. Ibid, 34

    12. William Greider, Secrets of the Temple: How the Federal Reserve Runs the Country, New York: Simon and Schuster, 1987, 276

    13. John Kenneth Galbraith, Money: Whence it Came, Where it Went, Houghton Mifflin Company, Boston, 1975, 121-122

    14. William Greider, op.cit., 277

    15. H.W. Brands, ‘He Is My Independent Self’, The Washington Post: June 11, 2006:www.washingtonpost.com/wp-dyn/content/article/2006/06/08/AR2006060801104.html

    16. CFR, ‘Continuing the Inquiry. History of CFR’: www.cfr.org/about/history/cfr/inquiry.html

    17. Chatham House, ‘CHATHAM HOUSE (The Royal Institute of International Affairs): Background’, Chatham House History: www.chathamhouse.org.uk/about/history/

    18. Carroll Quigley, The Anglo-American Establishment, op.cit., 5

    19. Carroll Quigley, Tragedy and Hope, op.cit., 132-133

    20. James G. McGann, Ph.D., The Global “Go-To Think Tanks”: The Leading Public Policy Research Organizations In The World, The Think Tanks and Civil Societies Program: University of Pennsylvania, International Relations Program, 2008, 26-28

    21. CBC, ‘Informal forum or global conspiracy?’, CBC News Online: June 13, 2006:www.cbc.ca/news/background/bilderberg-group/

    22. Holly Sklar, ed., Trilateralism: The Trilateral Commission and Elite Planning for World Management, South End Press: 1980, 161-171

    23. Glen McGregor, ‘Secretive power brokers meeting coming to Ottawa?’, Ottawa Citizen: May 24, 2006

    24. Holly Sklar, ed., op.cit., 76-78

    25. Edwin Black, War Against the Weak: Eugenics and America’s Campaign to Create a Master Race, New York: Thunders’s Mouth Press, 2004, 93

    26. Ibid, 18

    27. Ibid, 101-102

    28. Edwin Black, ‘Eugenics and the Nazis – the California connection’, The San Francisco Chronicle: November 9, 2003

    29. Edwin Black, War Against the Weak, op.cit., 396

    30. Ibid, 398

    31. Ibid, 416

    32. Ibid, 418

    33. Michael Barker, The Liberal Foundations of Environmentalism: Revisiting the Rockefeller-Ford Connection, Capitalism Nature Socialism: 19, (2), June 2008, 18

    34. Ibid, 19-20

    35. John Harlow, ‘Billionaire club in bid to curb overpopulation’, Times Online: May 24, 2009

    36. CFR, Remarks at the Council on Foreign Relations Annual Corporate Conference, Transcripts: March 10, 2005:www.cfr.org/publication/7908/remarks_at_the_council_on_foreign_relations_annual_corporate_conference.html

    37. CFR, Council on Foreign Relations Special Symposium in honor of David Rockefeller’s 90th Birthday, Transcript: May 23, 2005:www.cfr.org/publication/8133/council_on_foreign_relations_special_symposium_in_honor_of_david_rockefellers_90th_birthday.html

    38. David Rockefeller, Memoirs, New York: Random House: 2002, 405

    The above article appeared in New Dawn No. 118 (Jan-Feb 2010).

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    Who Really Runs the World? Conspiracies, Hidden Agendas & the Plan for World Government May 22, 2013 Andrew Gavin Marshall, New Dawn Waking Times So, who runs the world? It’s a question that people have struggled with since people began to struggle. It’s certainly a question with many interpretations, and incites answers of many varied perspectives. Often, it is relegated to the realm of “conspiracy theory,” in that, those who discuss this question or propose answers to it, are purveyors of a conspiratorial view of the world. However, it is my intention to discard the labels, which seek to disprove a position without actually proving anything to the contrary. One of these labels – “conspiracy theorist” – does just that: it’s very application to a particular perspective or viewpoint has the intention of “disproving without proof;” all that is needed is to simply apply the label. What I intend to do is analyse the social structure of the transnational ruling class, the international elite, who together run the world. This is not a conspiratorial opinion piece, but is an examination of the socially constructed elite class of people; what is the nature of power, how does it get used, and who holds it? A Historical Understanding of Power In answering the question “Who Runs the World?” we must understand what positions within society hold the most power, and thus, the answer becomes clear. If we simply understand this as heads of state, the answer will be flawed and inaccurate. We must examine the globe as a whole, and the power structures of the global political economy. The greatest position of power within the global capitalist system lies in the authority of money-creation: the central banking system. The central banking system, originating in 1694 in England, consists of an international network of central banks that are privately owned by wealthy shareholders and are granted governmental authority to print and issue a nation’s currency, and set interest rates, collecting revenue and making profit through the interest charged. Central banks give loans to both governments and industries, controlling both simultaneously. The ultimate centre of power in the central banking system is at the Bank for International Settlements (BIS), in Basle, Switzerland; which is the central bank to the world’s central banks, and is also a private bank owned by the world’s central banks. As Georgetown University history professor Carroll Quigley wrote: [T]he powers of financial capitalism had another far-reaching aim, nothing less than to create a world system of financial control in private hands able to dominate the political system of each country and the economy of the world as a whole. This system was to be controlled in a feudalist fashion by the central banks of the world acting in concert, by secret agreements arrived at in frequent private meetings and conferences. The apex of the system was to be the Bank for International Settlements in Basle, Switzerland, a private bank owned and controlled by the world’s central banks which were themselves private corporations.1 The central banks, and thus the central banking system as a whole, is a privately owned system in which the major shareholders are powerful international banking houses. These international banking houses emerged in tandem with the evolution of the central banking system. The central banking system first emerged in London, and expanded across Europe with time. With that expansion, the European banking houses also rose and expanded across the continent. The French Revolution resulted with Napoleon coming to power, who granted the French bankers a central bank of France, which they privately controlled.2 It was also out of the French Revolution that one of the major banking houses of the world emerged, the Rothschilds. Emerging out of a European Jewish ghetto, the Rothschilds quickly rose to the forefront in banking, and established banking houses in London, Paris, Frankfurt, Vienna and Naples, allowing them to profit off of all sides in the Napoleonic wars.3 As Carroll Quigley wrote in his monumental Tragedy and Hope, “The merchant bankers of London had already at hand in 1810-1850 the Stock Exchange, the Bank of England, and the London money market,” and that: In time they brought into their financial network the provincial banking centres, organised as commercial banks and savings banks, as well as insurance companies, to form all of these into a single financial system on an international scale which manipulated the quantity and flow of money so that they were able to influence, if not control, governments on one side and industries on the other.4 At the same time, in the United States, we saw the emergence of a powerful group of bankers and industrialists, such as the Morgans, Astors, Vanderbilts, Rockefellers, and Carnegies, and they created massive industrial monopolies and oligopolies throughout the 19th century.5 These banking interests were very close to and allied with the powerful European banking houses. The European, and particularly the British elites of the time, were beginning to organise their power in an effort to properly exert their influence internationally. At this time, European empires were engaging in the Scramble for Africa, in which nearly the entire continent of Africa, save Ethiopia, was colonised and carved up by European nations. One notable imperialist was Cecil Rhodes who made his fortune from diamond and gold mining in Africa with financial support from the Rothschilds,6 and “at that time [had] the biggest concentration of financial capital in the world.”7 Cecil Rhodes was also known for his radical views regarding America, particularly in that he would “talk with total seriousness of ‘the ultimate recovery of the United States of America as an integral part of the British Empire’.”8 Rhodes saw himself not simply as a moneymaker, but primarily as an “empire builder.” As Carroll Quigley explained, in 1891 three British elites met with the intent to create a secret society. The three men were Cecil Rhodes, William T. Stead, a prominent journalist of the day, and Reginald Baliol Brett, a “friend and confidant of Queen Victoria, and later to be the most influential adviser of King Edward VII and King George V.” Within this secret society, “real power was to be exercised by the leader, and a ‘Junta of Three.’ The leader was to be Rhodes, and the Junta was to be Stead, Brett, and Alfred Milner.”9 The purpose of this secret society, which was later headed by Alfred Milner, was: “The extension of British rule throughout the world, the perfecting of a system of emigration from the United Kingdom and of colonisation by British subjects of all lands wherein the means of livelihood are attainable by energy, labour, and enterprise… [with] the ultimate recovery of the United States of America as an integral part of a British Empire.” [Emphasis added]10 Essentially, it outlined a British-led cosmopolitical world order, one global system of governance under British hegemony. Among key players within this group were the Rothschilds and other banking interests.11 After the 1907 banking panic in the US, instigated by JP Morgan, pressure was placed upon the American political establishment to create a “stable” banking system. In 1910, a secret meeting of financiers was held on Jekyll Island, where they planned for the “creation of a National Reserve Association with fifteen major regions, controlled by a board of commercial bankers but empowered by the federal government to act like a central bank – creating money and lending reserves to private banks.”12 It was largely Paul M. Warburg, a Wall Street investment banker, who “had come up with a design for a single central bank [in 1910]. He called it the United Reserve Bank. From this and his later service on the first Federal Reserve Board, Warburg has, with some justice, been called the father of the System.”13President Woodrow Wilson followed the plan almost exactly as outlined by the Wall Street financiers, and added to it the creation of a Federal Reserve Board in Washington, which the President would appoint.14 Thus, true power in the world order was held by international banking houses, which privately owned the global central banking system, allowing them to control the credit of nations, and finance and control governments and industry. However, though the economic system was firmly in their control, allowing them to establish influence over finance, they needed to shape elite ideology accordingly. In effect, what was required was to socially construct a ruling class, internationally, which would serve their interests. To do this, these bankers set out to undertake a project of establishing think tanks to organise elites from politics, economics, academia, media, and the military into a generally cohesive and controllable ideology. Constructing a Ruling Class: Rise of the Think Tanks During World War I, a group of American scholars were tasked with briefing “Woodrow Wilson about options for the postwar world once the Kaiser and imperial Germany fell to defeat.” This group was called, “The Inquiry.” The group advised Wilson mostly through his trusted aide, Col. Edward M. House, who was Wilson’s “unofficial envoy to Europe during the period between the outbreak of World War I in 1914 and the intervention by the United States in 1917,” and was the prime driving force in the Wilson administration behind the establishment of the Federal Reserve System.15 “The Inquiry” laid the foundations for the creation of the Council on Foreign Relations (CFR), the most powerful think tank in the US and, “The scholars of the Inquiry helped draw the borders of post World War I central Europe.” On May 30, 1919, a group of scholars and diplomats from Britain and the US met at the Hotel Majestic, where they “proposed a permanent Anglo-American Institute of International Affairs, with one branch in London, the other in New York.” When the scholars returned from Paris, they were met with open arms by New York lawyers and financiers, and together they formed the Council on Foreign Relations in 1921. The “British diplomats returning from Paris had made great headway in founding their Royal Institute of International Affairs.” The Anglo-American Institute envisioned in Paris, with two branches and combined membership was not feasible, so both the British and American branches retained national membership, however, they would cooperate closely with one another.16 They were referred to, and still are, as “Sister Institutes.”17 The Milner Group, the secret society formed by Cecil Rhodes, “dominated the British delegation to the Peace Conference of 1919; it had a great deal to do with the formation and management of the League of Nations and of the system of mandates; it founded the Royal Institute of International Affairs in 1919 and still controls it.”18 There were other groups founded in many countries representing the same interests of the secret Milner Group, and they came to be known as the Round Table Groups, preeminent among them were the Royal Institute of International Affairs (Chatham House), the Council on Foreign Relations in the United States, and parallel groups were set up in Canada, Australia, New Zealand, South Africa and India.19 These were, in effect, the first international think tanks, which remain today, and are in their respective nations, among the top, if not the most prominent think tanks. In 2008, a major study was done by the University of Philadelphia’s International Relations Program – the Think Tanks and Civil Societies Program – which sought to analyse and examine the most powerful and influential think tanks in the world. While it is a useful resource to understanding the influence of think tanks, there is a flaw in its analysis. It failed to take into account the international origins of the Round Table Group think tanks, particularly the Council on Foreign Relations in the United States; Chatham House or the Royal Institute of International Affairs in London; the Canadian Institute of International Affairs, now renamed the Canadian International Council; and their respective sister organisations in India, South Africa, New Zealand and Australia. Further nations have since added to this group of related think tanks, including Germany, and a recently established European Council on Foreign Relations. The report, while putting focus on the international nature of think tanks, analysed these ones as separate institutions without being related or affiliated. This has, in effect, skewed the results of the study. However, it is still useful to examine. The top think tanks in the United States include the Council on Foreign Relations, (which was put at number 2, however, should be placed at the number 1 spot), the Brookings Institution, (which was inaccurately given the position of number one), the Carnegie Endowment for International Peace, RAND Corporation, Heritage Foundation, Woodrow Wilson International Centre for Scholars, the Center for Strategic and International Studies, and the American Enterprise Institute, among others. The top think tanks in the world, outside of the United States, are Chatham House (sitting at number one), the International Institute for Strategic Studies in the UK, the German Council on Foreign Relations, the French Institute of International Relations, the Adam Smith Institute in the UK, the Fraser Institute in Canada, the European Council on Foreign Relations, the International Crisis Group in Belgium, and the Canadian Institute of International Affairs.20 In 1954, the Bilderberg Group was founded in the Netherlands. Every year since then the group holds a secretive meeting, drawing roughly 130 of the political-financial-military-academic-media elites from North America and Western Europe as “an informal network of influential people who could consult each other privately and confidentially.”21 Regular participants include the CEOs or Chairmen of some of the largest corporations in the world, oil companies such as Royal Dutch Shell, British Petroleum, and Total SA, as well as various European monarchs, international bankers such as David Rockefeller, major politicians, presidents, prime ministers, and central bankers of the world.22 The Bilderberg Group acts as a “secretive global think-tank,” with an original intent “to link governments and economies in Europe and North America amid the Cold War.”23 In 1970, David Rockefeller became Chairman of the Council on Foreign Relations, while also being Chairman and CEO of Chase Manhattan. In 1970, an academic who joined the Council on Foreign Relations in 1965 wrote a book called Between Two Ages: America’s Role in the Technetronic Era. The author, Zbigniew Brzezinski, called for the formation of “A Community of the Developed Nations,” consisting of Western Europe, the United States and Japan. Brzezinski wrote about how “the traditional sovereignty of nation states is becoming increasingly unglued as transnational forces such as multinational corporations, banks, and international organisations play a larger and larger role in shaping global politics.” So, in 1972, David Rockefeller and Brzezinski “presented the idea of a trilateral grouping at the annual Bilderberg meeting.” In July of 1972, seventeen powerful people met at David Rockefeller’s estate in New York to plan for the creation of another grouping. Also at the meeting was Brzezinski, McGeorge Bundy, the President of the Ford Foundation, (brother of William Bundy, editor of Foreign Affairs) and Bayless Manning, President of the Council on Foreign Relations.24 In 1973, these people formed the Trilateral Commission, which acted as a sister organisation to Bilderberg, linking the elites of Western Europe, North America, and Japan into a transnational ruling class. These think tanks have effectively socially constructed an ideologically cohesive ruling class in each nation and fostered the expansion of international ideological alignment among national elites, allowing for the development of a transnational ruling class sharing a dominant ideology. These same interests, controlled by the international banking houses, had to socially construct society itself. To do this, they created a massive network of tax-exempt foundations and non-profit organisations, which shaped civil society according to their designs. Among the most prominent of these are the Carnegie Corporation, the Ford Foundation, and the Rockefeller Foundation. The “Foundations” of Civil Society These foundations shaped civil society by financing research projects and initiatives into major social projects, creating both a dominant world-view for the elite classes, as well as managing the other classes. These foundations, since their establishment, played a large part in the funding and organising of the eugenics movement, which helped facilitate this racist, elitist ideology to having enormous growth and influence, ultimately culminating in the Nazi Holocaust. From then, the word “eugenics” had to be dropped from the ideology and philanthropy of elites, and was replaced with new forms of eugenics policies and concepts. Among them, genetics, population control and environmentalism. These foundations also funded seemingly progressive and alternative media sources in an effort to control the opposition, and manage the resistance to their world order, essentially making it ineffective and misguided. The Rockefeller Foundation was established in 1912, and immediately began giving money to eugenics research organisations.25 Eugenics was a pseudo-scientific and social science movement that emerged in the late 19th century, and gained significant traction in the first half of the 20th century. One of the founding ideologues of eugenics, Sir Francis Galton, an anthropologist and cousin to Charles Darwin, wrote that eugenics “is the study of all agencies under social control which can improve or impair the racial quality of future generations.”26 Ultimately, it was about the “sound” breeding of people and maintaining “purity” and “superiority” of the blood. It was an inherently racist ideology, which saw all non-white racial categories of people as inherently and naturally inferior, and sought to ground these racist theories in “science.” The vast wealth and fortunes of the major industrialists and bankers in the United States flowed heavily into the eugenics organisations, promoting and expanding this racist and elitist ideology. Money from the Harriman railroad fortune, with millions given by the Rockefeller and Carnegie family fortunes were subsequently “devoted to sterilisation of several hundred thousands of American ‘defectives’ annually, as a matter of eugenics.”27 In the United States, 27 states passed eugenics based sterilisation laws of the “unfit,” which ultimately led to the sterilisation of over 60,000 people. Throughout the 1920s and 30s, the Carnegie and especially the Rockefeller Foundation, funded eugenics research in Germany, directly financing the Nazi scientists who perpetrated some of the greatest crimes of the Holocaust.28 Following the Holocaust, the word “eugenics” was highly discredited. Thus, these elites who wanted to continue with the implementation of their racist and elitist ideology desperately needed a new name for it. In 1939, the Eugenics Records Office became known as the Genetics Record Office.29 However, tens of thousands of Americans continued to be sterilised throughout the 40s, 50s and 60s, the majority of which were women.30 Edwin Black analysed how the pseudoscience of eugenics transformed into what we know as the science of genetics. In a 1943 edition of Eugenical News, an article titled “Eugenics After the War,” cited Charles Davenport, a major founder of eugenics, in his vision of “a new mankind of biological castes with master races in control and slave races serving them.”31 A 1946 article in Eugenical News stated that, “Population, genetics, [and] psychology, are the three sciences to which the eugenicist must look for the factual material on which to build an acceptable philosophy of eugenics and to develop and defend practical eugenics proposals.” As Black explained, “the incremental effort to transform eugenics into human genetics forged an entire worldwide infrastructure,” with the founding of the Institute for Human Genetics in Copenhagen in 1938, led by Tage Kemp, a Rockefeller Foundation eugenicist, and was financed with money from the Rockefeller Foundation.32 Today, much of civil society and major social projects are a product of these foundations, and align with various new forms of eugenics. The areas of population control and environmentalism are closely aligned and span a broad range of intellectual avenues. The major population control organisations emerged with funding from these various foundations, particularly the Rockefeller foundations and philanthropies. These organisations, such as the Rockefeller and Ford foundations, funded major civil society movements, such as the Civil Rights movement, in an effort to “create a wedge between social movement activists and their unpaid grassroots constituents, thereby facilitating professionalisation and institutionalisation within the movement,” ultimately facilitating a “narrowing and taming of the potential for broad dissent,” with an aim of limiting goals to “ameliorative rather than radical change.”33 Two major organisations in the development of the environmental movement were the Conservation Foundation and Resources for the Future, which were founded and funded with money from the Rockefeller and Ford Foundations, and helped “launch an explicitly pro-corporate approach to resource conservation.”34 Even the World Wildlife Fund was founded in the early 1960s by the former president of the British Eugenics Society, and its first President was Prince Bernhard of the Netherlands, a founding member of the Bilderberg Group. While the environmental movement positions people as the major problem for the earth, relating humanity to a cancer, population control becomes a significant factor in proposing environmental solutions. In May of 2009, a secret meeting of billionaire philanthropists took place in which they sought to coordinate how to “address” the world’s environmental, social, and industrial threats. Each billionaire at the meeting was given 15 minutes to discuss their “preferred” cause, and then they deliberated to create an “umbrella” cause to harness all their interests. The end result was that the umbrella cause for which the billionaires would aim to “give to” was population control, which “would be tackled as a potentially disastrous environmental, social and industrial threat.” Among those present at the meeting were David Rockefeller, Jr., George Soros, Warren Buffet, Michael Bloomberg, Ted Turner, Bill Gates, and even Oprah Winfrey.35 Conclusion At the top of the list of those who run the world, we have the major international banking houses, which control the global central banking system. From there, these dynastic banking families created an international network of think tanks, which socialised the ruling elites of each nation and the international community as a whole, into a cohesive transnational elite class. The foundations they established helped shape civil society both nationally and internationally, playing a major part in the funding – and thus coordinating and co-opting – of major social-political movements. An excellent example of one member of the top of the hierarchy of the global elite is David Rockefeller, patriarch of the Rockefeller family. Long serving as Chairman and CEO of Chase Manhattan bank, he revolutionised the notion of building a truly global bank. He was also Chairman of the Council on Foreign Relations, a founding member of Bilderberg and the Trilateral Commission, heavily involved in the family philanthropies, and sits atop a vast number of boards and foundations. Even Alan Greenspan, in a speech to the Council on Foreign Relations, said that David Rockefeller and the CFR have, “in many respects, formulated the foreign policy of this country.”36 In another speech to the Council on Foreign Relations, then World Bank President James Wolfesohn, said in 2005, in honour of David Rockefeller’s 90th birthday, that, “the person who had perhaps the greatest influence on my life professionally in this country, and I’m very happy to say personally there afterwards, is David Rockefeller.” He then said, “In fact, it’s fair to say that there has been no other single family influence greater than the Rockefeller’s in the whole issue of globalisation and in the whole issue of addressing the questions which, in some ways, are still before us today. And for that David, we’re deeply grateful to you and for your own contribution in carrying these forward in the way that you did.”37 David Rockefeller, himself, wrote, “For more than a century ideological extremists at either end of the political spectrum have seized upon well-publicised incidents such as my encounter with Castro to attack the Rockefeller family for the inordinate influence they claim we wield over American political and economic institutions. Some even believe we are part of a secret cabal working against the best interests of the United States, characterising my family and me as ‘internationalists’ and of conspiring with others around the world to build a more integrated global political and economic structure – one world, if you will. If that’s the charge, I stand guilty, and I am proud of it.”38 About the Author ANDREW G. MARSHALL is a Research Associate with the Centre for Research on Globalization based out of Montreal, Canada (www.globalresearch.ca). He has written extensively on issues imperialism in the Middle East and Africa, the environment, Homeland Security, war, terrorism and the global economy. He is currently studying Global Political Economy and the History of the Middle East and Africa at Simon Fraser University (Canada). Footnotes: 1. Carroll Quigley, Tragedy and Hope: A History of the World in Our Time, New York: Macmillan Company, 1966, 324 2. Carroll Quigley, op.cit., 515; Robert Elgie and Helen Thompson, ed., The Politics of Central Banks, New York: Routledge, 1998, 97-98 3. Sylvia Nasar, ‘Masters of the Universe’, The New York Times: January 23, 2000; ‘The Family That Bankrolled Europe’, BBC News: July 9, 1999, http://news.bbc.co.uk/1/hi/uk/389053.stm 4. Carroll Quigley, op.cit., 51 5. Howard Zinn, A People’s History of the United States, Harper Perennial: New York, 2003, 323 6. Carroll Quigley, op.cit., 130 7. Niall Ferguson, Empire: The Rise and Demise of the British World Order and the Lessons for Global Power, New York: Basic Books, 2004, 186 8. Ibid, 190 9. Carroll Quigley, The Anglo-American Establishment, GSG & Associates, 1981, 3 10. Ibid, 33 11. Ibid, 34 12. William Greider, Secrets of the Temple: How the Federal Reserve Runs the Country, New York: Simon and Schuster, 1987, 276 13. John Kenneth Galbraith, Money: Whence it Came, Where it Went, Houghton Mifflin Company, Boston, 1975, 121-122 14. William Greider, op.cit., 277 15. H.W. Brands, ‘He Is My Independent Self’, The Washington Post: June 11, 2006:www.washingtonpost.com/wp-dyn/content/article/2006/06/08/AR2006060801104.html 16. CFR, ‘Continuing the Inquiry. History of CFR’: www.cfr.org/about/history/cfr/inquiry.html 17. Chatham House, ‘CHATHAM HOUSE (The Royal Institute of International Affairs): Background’, Chatham House History: www.chathamhouse.org.uk/about/history/ 18. Carroll Quigley, The Anglo-American Establishment, op.cit., 5 19. Carroll Quigley, Tragedy and Hope, op.cit., 132-133 20. James G. McGann, Ph.D., The Global “Go-To Think Tanks”: The Leading Public Policy Research Organizations In The World, The Think Tanks and Civil Societies Program: University of Pennsylvania, International Relations Program, 2008, 26-28 21. CBC, ‘Informal forum or global conspiracy?’, CBC News Online: June 13, 2006:www.cbc.ca/news/background/bilderberg-group/ 22. Holly Sklar, ed., Trilateralism: The Trilateral Commission and Elite Planning for World Management, South End Press: 1980, 161-171 23. Glen McGregor, ‘Secretive power brokers meeting coming to Ottawa?’, Ottawa Citizen: May 24, 2006 24. Holly Sklar, ed., op.cit., 76-78 25. Edwin Black, War Against the Weak: Eugenics and America’s Campaign to Create a Master Race, New York: Thunders’s Mouth Press, 2004, 93 26. Ibid, 18 27. Ibid, 101-102 28. Edwin Black, ‘Eugenics and the Nazis – the California connection’, The San Francisco Chronicle: November 9, 2003 29. Edwin Black, War Against the Weak, op.cit., 396 30. Ibid, 398 31. Ibid, 416 32. Ibid, 418 33. Michael Barker, The Liberal Foundations of Environmentalism: Revisiting the Rockefeller-Ford Connection, Capitalism Nature Socialism: 19, (2), June 2008, 18 34. Ibid, 19-20 35. John Harlow, ‘Billionaire club in bid to curb overpopulation’, Times Online: May 24, 2009 36. CFR, Remarks at the Council on Foreign Relations Annual Corporate Conference, Transcripts: March 10, 2005:www.cfr.org/publication/7908/remarks_at_the_council_on_foreign_relations_annual_corporate_conference.html 37. CFR, Council on Foreign Relations Special Symposium in honor of David Rockefeller’s 90th Birthday, Transcript: May 23, 2005:www.cfr.org/publication/8133/council_on_foreign_relations_special_symposium_in_honor_of_david_rockefellers_90th_birthday.html 38. David Rockefeller, Memoirs, New York: Random House: 2002, 405 The above article appeared in New Dawn No. 118 (Jan-Feb 2010). If you appreciated this article, please consider a digital subscription to New Dawn. © New Dawn Magazine and the respective author. © Copyright New Dawn Magazine, http://www.newdawnmagazine.com. Permission granted to freely distribute this article for non-commercial purposes if unedited and copied in full, including this notice. © Copyright New Dawn Magazine, http://www.newdawnmagazine.com. Permission to re-send, post and place on web sites for non-commercial purposes, and if shown only in its entirety with no changes or additions. This notice must accompany all re-posting. ~~ Help Waking Times to raise the vibration by sharing this article with the buttons below… https://www.wakingtimes.com/who-really-runs-the-world-conspiracies-hidden-agendas-the-plan-for-world-government/
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  • Predictive Programming, Symbolism, and Ideological Subversion at Olympic Games Opening Ceremonies

    A tool that has been used as part of the ideological subversion of society is predictive programming – the process of informing and conditioning the population about events that are soon to occur. For example, in years previous to the 2020 Covid fake pandemic masses of people were conditioned to be scared about worldwide pandemics and deadly killer viruses. Several movies and television series were produced about a worldwide coronavirus pandemic. Examples include ‘Dead Plague’ and ‘Contagion’. ’Contagion’ was based on a coronavirus pandemic with lockdowns, social distancing, face masks, etc., being introduced. The Covid fake pandemic that later occurred was predicted in detail in these movies – the population had also been primed to accept it.

    London Olympics 2012

    Remember the London Olympics 2012 opening ceremony?

    Doctors and nurses dancing around children in hospital beds. A massive figure of death holding a needle. This was a prime example of how they condition the masses to accept a generated reality soon to occur. The statistics of death and injury related to Covid vaccination have been documented by many doctors and researchers, for example by Professor Chossudovsky on the Global Research website, and in one of my own books.



    Beijing Winter Olympics 2022

    At the Beijing Winter Olympics 2022 each team carried a snowflake aloft seemingly paying homage to what we were told was a ‘snowflake of winter’. The 6-pointed snowflake symbol was the centrepiece of the entire ceremony. Yet in the freeze-frame below we see the snowflake seemingly transform into the 6-pointed star symbol of Zionist Israel. Why did this occur? Was this a co-incidence?





    See also this article on the ancient origins of this hijacked symbol.



    The satkona is the oldest spiritual symbol known to the world. In the oldest known Vedic literature, Sri Brahma-samhita, the Sat-kona is mentioned in a description of the supreme abode of Goloka, the abode of Krsna, God personified in ancient Vedic literature

    The use of the satkona is evidenced in ancient Vedic cultures dating back over 5,000 years ago. The satkona has been used throughout the ages in India, Nepal, China, Tibet, Sri Lanka, and other countries in Asia by proponents of Vedic Vaisnavism, Jainism, and also in Buddhism.

    Paris Olympics 2024

    The recent opening ceremony for the Paris Olympics did not seem to be about sport rather something else entirely. The event has come under heavy criticism from people worldwide with conservative, traditional, and God-conscious values. The event was filled with woke left-wing symbolism, overt perversity, and seemingly pagan or satanic references. Personally I felt like washing my eyes out as quickly as possible.

    One of the scenes that sparked particular controversy was of a table of drag queens with one in the middle wearing some form of crown or halo on her head and standing in front of DJ gear. The already infamous scene appeared to be a recreation and mockery of Leonardo da Vinci’s mural of Jesus and his Twelve Apostles at table of the Last Supper. Was this an intentional replacement of Jesus and the disciples at the Last Supper with men in drag? Was this an intentional mockery of those with Christian faith?

    “One of the main performances of the Olympics was an LGBT mockery of a sacred Christian story – the Last Supper – the last supper of Christ. The apostles were portrayed by transvestites,” the spokesperson for Russia’s Foreign Ministry, Maria Zakharova, posted on Telegram.

    We were then presented with a naked blue man in flower garlands singing suggestive lyrics and pointing at his groin. This was apparently supposed to represent Dionysus, the Greek god of wine and ecstasy. However, this could also be interpreted as a mockery of Lord Krishna, who is described in the ancient Vedic scriptures as an avatar of God who lived on Earth 5,000 years. Regardless of the truth of the matter, the whole spectacle was in appallingly bad taste.



    French singer Philippe Katerine during the Paris Olympics opening ceremony(X/@Scipionista)

    The ceremony was littered with pre-recorded scenes with references to non-traditional sexual inclinations that left many viewers aghast. It appeared to be an overt display of LGBTQ+ perversity and sexual abandonment, containing a bearded drag queen crawling on all fours; the beginnings of a menage à trois; and an intimate embrace between two men who danced, hugged, kissed and held hands. The in-your-face nature of the show seemed to be an insult to people with conservative or God-conscious values. I for one would not allow impressionable children to watch this degrading melee.

    The athletes themselves were paraded and welcomed down the River Seine in many boats. Was this a mind programming reference to the huge numbers immigrants from faraway places that have been arriving in boats to Europe for years now? The people of Europe, it seems, are meant to welcome and accept mass (often unvetted) immigration regardless of the consequences and well documented increases in crime. Meanwhile, mere days before the opening ceremony a 25-year Australian woman, a tourist, was allegedly gang raped in Paris by 5 men of an immigrant background, see this report.

    Rejecting Indoctrination and Mind Control – The Value of Discernment

    The woke left, hypnotised by decades of new world order propaganda have welcomed and embraced bogus and perverse socio-political agendas. Sports events, TV, internet, and AI neuromancers channel corporate-funded propaganda and thought controls to the minds of the masses. These are mind control wands of the globalists.

    When we hear about ‘multi-culturalism’ and ‘diversity’ in the woke political sense – what does it actually mean? The entire world has been multi-cultural for thousands of years before this funded political agenda. Why are these code words and ideologies so embedded into the cultural psyche? Who is funding the subversion of America and the wider world with these ideological agendas?

    There is value in discernment, and in distinguishing good from evil. An increasingly perverse and dangerous ideological culture has been foisted upon us all. It can be rejected, and a more God-conscious life can be embraced. Perverse and toxic lifestyles devalue God-given life force (chi), and brain force – see also this article. Life is a mirror not a window, and surely a purified God-conscious life demands internal God-conscious values.

    Will those that carry out demonic actions will be subject to karma? The Christian teaching is that “whatever a man sows, this he will also reap.” I am also reminded of the words of Bhaktivedanta Swami Prabhupada, a great saint in the Vedic tradition of devotion to God.

    “… you have got a short duration of life… The best thing is that you mold your life and go back to home, back to Godhead. Oil your own machine, instead of thinking what will happen elsewhere. [Those things] will happen. Because people will go on with their rascal civilization, natural consequences will be there.”

    *

    Click the share button below to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles.

    Spread the Truth, Refer a Friend to Global Research

    Mark Keenan, is a former scientist at the UK Government Dept. of Energy and Climate Change, and at the United Nations Environment Division. He is a Research Associate of the Centre for Research on Globalization (CRG). He is author of the following books available on amazon.com:

    Transcending the Climate Change Deception Toward Real Sustainability
    CO2 Climate Hoax – How Bankers Hijacked the Real Environment Movement
    Godless Fake Science
    No Worries No Virus
    Demonic Economics and the Tricks of the Bankers
    Fake Moon Landings and the Lies of NASA
    Censored History of WW2 and Communism
    Website: Reality Distinguished From Illusion


    https://www.globalresearch.ca/predictive-programming-symbolism-ideological-subversion-olympic-games-opening-ceremonies/5864251
    Predictive Programming, Symbolism, and Ideological Subversion at Olympic Games Opening Ceremonies A tool that has been used as part of the ideological subversion of society is predictive programming – the process of informing and conditioning the population about events that are soon to occur. For example, in years previous to the 2020 Covid fake pandemic masses of people were conditioned to be scared about worldwide pandemics and deadly killer viruses. Several movies and television series were produced about a worldwide coronavirus pandemic. Examples include ‘Dead Plague’ and ‘Contagion’. ’Contagion’ was based on a coronavirus pandemic with lockdowns, social distancing, face masks, etc., being introduced. The Covid fake pandemic that later occurred was predicted in detail in these movies – the population had also been primed to accept it. London Olympics 2012 Remember the London Olympics 2012 opening ceremony? Doctors and nurses dancing around children in hospital beds. A massive figure of death holding a needle. This was a prime example of how they condition the masses to accept a generated reality soon to occur. The statistics of death and injury related to Covid vaccination have been documented by many doctors and researchers, for example by Professor Chossudovsky on the Global Research website, and in one of my own books. Beijing Winter Olympics 2022 At the Beijing Winter Olympics 2022 each team carried a snowflake aloft seemingly paying homage to what we were told was a ‘snowflake of winter’. The 6-pointed snowflake symbol was the centrepiece of the entire ceremony. Yet in the freeze-frame below we see the snowflake seemingly transform into the 6-pointed star symbol of Zionist Israel. Why did this occur? Was this a co-incidence? See also this article on the ancient origins of this hijacked symbol. The satkona is the oldest spiritual symbol known to the world. In the oldest known Vedic literature, Sri Brahma-samhita, the Sat-kona is mentioned in a description of the supreme abode of Goloka, the abode of Krsna, God personified in ancient Vedic literature The use of the satkona is evidenced in ancient Vedic cultures dating back over 5,000 years ago. The satkona has been used throughout the ages in India, Nepal, China, Tibet, Sri Lanka, and other countries in Asia by proponents of Vedic Vaisnavism, Jainism, and also in Buddhism. Paris Olympics 2024 The recent opening ceremony for the Paris Olympics did not seem to be about sport rather something else entirely. The event has come under heavy criticism from people worldwide with conservative, traditional, and God-conscious values. The event was filled with woke left-wing symbolism, overt perversity, and seemingly pagan or satanic references. Personally I felt like washing my eyes out as quickly as possible. One of the scenes that sparked particular controversy was of a table of drag queens with one in the middle wearing some form of crown or halo on her head and standing in front of DJ gear. The already infamous scene appeared to be a recreation and mockery of Leonardo da Vinci’s mural of Jesus and his Twelve Apostles at table of the Last Supper. Was this an intentional replacement of Jesus and the disciples at the Last Supper with men in drag? Was this an intentional mockery of those with Christian faith? “One of the main performances of the Olympics was an LGBT mockery of a sacred Christian story – the Last Supper – the last supper of Christ. The apostles were portrayed by transvestites,” the spokesperson for Russia’s Foreign Ministry, Maria Zakharova, posted on Telegram. We were then presented with a naked blue man in flower garlands singing suggestive lyrics and pointing at his groin. This was apparently supposed to represent Dionysus, the Greek god of wine and ecstasy. However, this could also be interpreted as a mockery of Lord Krishna, who is described in the ancient Vedic scriptures as an avatar of God who lived on Earth 5,000 years. Regardless of the truth of the matter, the whole spectacle was in appallingly bad taste. French singer Philippe Katerine during the Paris Olympics opening ceremony(X/@Scipionista) The ceremony was littered with pre-recorded scenes with references to non-traditional sexual inclinations that left many viewers aghast. It appeared to be an overt display of LGBTQ+ perversity and sexual abandonment, containing a bearded drag queen crawling on all fours; the beginnings of a menage à trois; and an intimate embrace between two men who danced, hugged, kissed and held hands. The in-your-face nature of the show seemed to be an insult to people with conservative or God-conscious values. I for one would not allow impressionable children to watch this degrading melee. The athletes themselves were paraded and welcomed down the River Seine in many boats. Was this a mind programming reference to the huge numbers immigrants from faraway places that have been arriving in boats to Europe for years now? The people of Europe, it seems, are meant to welcome and accept mass (often unvetted) immigration regardless of the consequences and well documented increases in crime. Meanwhile, mere days before the opening ceremony a 25-year Australian woman, a tourist, was allegedly gang raped in Paris by 5 men of an immigrant background, see this report. Rejecting Indoctrination and Mind Control – The Value of Discernment The woke left, hypnotised by decades of new world order propaganda have welcomed and embraced bogus and perverse socio-political agendas. Sports events, TV, internet, and AI neuromancers channel corporate-funded propaganda and thought controls to the minds of the masses. These are mind control wands of the globalists. When we hear about ‘multi-culturalism’ and ‘diversity’ in the woke political sense – what does it actually mean? The entire world has been multi-cultural for thousands of years before this funded political agenda. Why are these code words and ideologies so embedded into the cultural psyche? Who is funding the subversion of America and the wider world with these ideological agendas? There is value in discernment, and in distinguishing good from evil. An increasingly perverse and dangerous ideological culture has been foisted upon us all. It can be rejected, and a more God-conscious life can be embraced. Perverse and toxic lifestyles devalue God-given life force (chi), and brain force – see also this article. Life is a mirror not a window, and surely a purified God-conscious life demands internal God-conscious values. Will those that carry out demonic actions will be subject to karma? The Christian teaching is that “whatever a man sows, this he will also reap.” I am also reminded of the words of Bhaktivedanta Swami Prabhupada, a great saint in the Vedic tradition of devotion to God. “… you have got a short duration of life… The best thing is that you mold your life and go back to home, back to Godhead. Oil your own machine, instead of thinking what will happen elsewhere. [Those things] will happen. Because people will go on with their rascal civilization, natural consequences will be there.” * Click the share button below to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. Spread the Truth, Refer a Friend to Global Research Mark Keenan, is a former scientist at the UK Government Dept. of Energy and Climate Change, and at the United Nations Environment Division. He is a Research Associate of the Centre for Research on Globalization (CRG). He is author of the following books available on amazon.com: Transcending the Climate Change Deception Toward Real Sustainability CO2 Climate Hoax – How Bankers Hijacked the Real Environment Movement Godless Fake Science No Worries No Virus Demonic Economics and the Tricks of the Bankers Fake Moon Landings and the Lies of NASA Censored History of WW2 and Communism Website: Reality Distinguished From Illusion https://www.globalresearch.ca/predictive-programming-symbolism-ideological-subversion-olympic-games-opening-ceremonies/5864251
    WWW.GLOBALRESEARCH.CA
    Predictive Programming, Symbolism, and Ideological Subversion at Olympic Games Opening Ceremonies
    A tool that has been used as part of the ideological subversion of society is predictive programming – the process of informing and conditioning the population about events that are soon to occur. For example, in years previous to the 2020 Covid fake pandemic masses of people were conditioned to be scared about worldwide pandemics …
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  • HUGE: Covid nasal swabs ruled ”UNLAWFUL” by Ontario court
    This is big news.

    Peter Imanuelsen

    AI generated image
    A court in Ontario, Canada has ruled that covid PCR nasal swabs were an ”unlawful requirement”.

    This is a big development.

    The court case revolves around a traveler that was returning home, but after arriving at Pearson International Airport on the 9th April 2022, she rejected a covid nasal swab test.

    She was then consequently convicted of failing to comply with the Quarantine Act, and got a fine that together with additional charges landed at a whopping $6,255

    The Judge ruled that this was not allowed, stating that ”the screening test cannot involve the insertion into the traveler’s body of any instrument or foreign body”.

    Paper straws SUCK - Contains TOXIC "forever chemicals"

    Paper straws SUCK - Contains TOXIC "forever chemicals"
    Further, the Judge said the following:

    ”I do decide that the nasal swab test...was an unlawful requirement or demand..refusal to comply with the requirement or demand was lawful on her part. Because the requirement or demand made of her by the screening officer was not lawful”

    So there we have it.

    A court in Canada has ruled that it was ILLEGAL to force people to be nasal swabbed.

    When you think about it, how on earth was it considered acceptable for people to be forced to get a foreign object poked up their nose to begin with? My body, my choice!

    I did get some nasal swabs when I had to travel during covid, and let me tell you, it was not a pleasant experience at all.

    The good news is that it is new recognized as being unlawful, which will be a good precedent going forward.

    Finally, some common sense is prevailing!

    Share

    https://substack.com/home/post/p-146561404
    HUGE: Covid nasal swabs ruled ”UNLAWFUL” by Ontario court This is big news. Peter Imanuelsen AI generated image A court in Ontario, Canada has ruled that covid PCR nasal swabs were an ”unlawful requirement”. This is a big development. The court case revolves around a traveler that was returning home, but after arriving at Pearson International Airport on the 9th April 2022, she rejected a covid nasal swab test. She was then consequently convicted of failing to comply with the Quarantine Act, and got a fine that together with additional charges landed at a whopping $6,255 The Judge ruled that this was not allowed, stating that ”the screening test cannot involve the insertion into the traveler’s body of any instrument or foreign body”. Paper straws SUCK - Contains TOXIC "forever chemicals" Paper straws SUCK - Contains TOXIC "forever chemicals" Further, the Judge said the following: ”I do decide that the nasal swab test...was an unlawful requirement or demand..refusal to comply with the requirement or demand was lawful on her part. Because the requirement or demand made of her by the screening officer was not lawful” So there we have it. A court in Canada has ruled that it was ILLEGAL to force people to be nasal swabbed. When you think about it, how on earth was it considered acceptable for people to be forced to get a foreign object poked up their nose to begin with? My body, my choice! I did get some nasal swabs when I had to travel during covid, and let me tell you, it was not a pleasant experience at all. The good news is that it is new recognized as being unlawful, which will be a good precedent going forward. Finally, some common sense is prevailing! Share https://substack.com/home/post/p-146561404
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  • Dr Peter McCullough Recommends Dodgey Synthetic siRNA Jabs to Counter Effects of Dodgey Synthetic mRNA Jabs
    You're in great hands, health freedom movement! Not.

    Anthony Colpo

    The Medical Freedom Movement is full of suspicious characters. So suspicious you'd almost think the movement has been captured, or even commandeered from the outset, by the same people who brought us the 2020 blockbuster "The Great Culling: This Time, it’s Global!”

    There's Steve Kirsch, the DARPA teen protege and Rockefeller-linked buffoon famous for The Most Important Surveys You'll Ever Do!!, big money challenges he has no intention of fulfilling, surveillance state and CBDC technology, and aggressive promotion of the highly toxic, suicide-inducing SSRI fluvoxamine.

    There's Robert "Sly" Malone, the self-proclaimed inventor of "mRNA vaccine technology" who cries hard-done-by while swimming around in billion$ of grant money from the US Military (major enablers of the globalist death shot campaign), all while pretending claiming to be an injured vaxxx victim.

    There's Brett Weinstein, who helped propel Kirsch and Malone into stardom with his June 11, 2021 Darkhorse Podcast. In this creepy snippet from his Tucker Carlson interview, Weinstein gushes like a lovesick teen over mRNA technology. Such impassioned praise for a technology with a 30-year track record of failure, one that was successfully deployed to trigger accelerated death and disability around the world, is extremely curious for someone presenting as a health freedom fighter.


    There's Dr Ryan Cole who, at "the first Conversation on Covid" in Puerto Rico September 2021, emphatically emphasized “Covid is a clotting disease. Covid is a clotting disease. Covid is a clotting disease.”

    In case you didn't catch it the first three times, Cole reckons COVID is a clotting disease.

    Bollocks. COVID is regular cold, flu and pneumonia renamed and packaged as an uber-deadly new threat. They are not "clotting diseases" but respiratory ailments. What is a clotting disease is the common and now well-documented life-threatening thrombosis caused by the Unsafe and Ineffective gene therapies to treat the renamed COVID caused by the never-isolated Sars-Cov-2. Despite this clotting effect of the vaxxxines being well-established by September 2021, Cole preferred to blame the phenomenon on 'COVID.'

    With health freedom heroes like this, who needs villains?


    The “remarkable” San Juan “Covid Conversation” where health freedom spokespeople not chosen by you acted as if COVID was real and not a globalist psy-op.
    There's Dr Pierre Kory who, at the same star-studded gathering of pandemic shills, described COVID, the artist formerly known as Cold’n’Flu, as "the most complex and most violent disease that I have seen and the most difficult to treat in the ICU.”

    COVID: Once a simple cold you sat out with some hot tea, lemon juice and Vaporub, now the most complex and violent thug of a disease the world of medicine has ever seen! If the madicine gig ever stops working out for Kory, he should migrate to Australia and get a job as a SAPOL prosecutor - with such an unbridled capacity for egregious nonsense, he'd fit right in.


    Dr Pierre Kory, supposed member of the Health Freedom Movement, pushing the mask farce in uber-mainstream USA Today.
    The ‘Respectable’ Face of Pandemic and Gene Therapy Propaganda?

    Then there's the movement's smiling enigma, Dr Peter McCullough. Depending on who you listen to, McCullough is either a controlled opposition shill or the most sincere bloke you could ever meet.

    Compared to some of the other suspect characters who comprise the upper echelons of the health freedom movement, there's something disarming about McCullough. He doesn't have the grating motor mouth of Kirsch, nor the sinister gaze and evil gnome vibe of Malone.

    McCullough appears the polar opposite of Kirsch, who comes off like the tech-nerd version of your obnoxious, balding, know-it-all Uncle Barry. The guy who slurps, farts, belches at family gatherings and blames it on the dog, and challenges his nephews to wrestling matches while drunk then refuses to concede defeat when they repeatedly pin his fat hairy shoulders to the ground.

    McCullough seems more like your Uncle Ronald, the successful physician who arrives at family gatherings with your charmingly demure and well-liked Auntie Mary in his late model Jaguar. He doesn't act like a bogan, doesn't antagonize his nephews, and generally presents as a jovial, amicable, clean-living guy.

    But from behind McCullough's disarming facade there emanates some very dubious claims. I started to smell the pungent odour of pharma-sponsored allopathic bullpoop, extra-strength version, when McCullough claimed toxic statin drugs reduced the risk of dementia and Alzheimers Disease.

    Anyone who even pretends to care about health and medical freedom has no business praising toxic and ineffective garbage like cholesterol-lowering statins.

    To make his claim, McCullough had to ignore the substantial volume of clinical trial evidence showing both low cholesterol and cholesterol reduction via statins not only fail to prevent dementia and Alzheimers Disease, but often result in cognitive and neurological harms. Cholesterol is an integral component of your brain and nerve sheaths - claiming you can prevent cognitive and neurological decline by lowering cholesterol is like claiming your car will drive further and longer after you drain half the fuel from the tank. It is an inherently absurd and false thing to claim.

    McCullough, however, appears to have no issue with making inherently absurd and false claims. Because the RCT evidence wouldn't support his beloved statins, he instead based his untenable claims entirely upon a a 2022 meta-analysis of epidemiological studies by Italian researchers - two of whom have extensive ties to pharma companies, including cholesterol-lowering drug manufacturers like Pfizer, Merck, Amgen, Servier and Sanofi-Regeneron.

    Just brilliant.

    No matter how you wish to frame it, McCullough has benefited handsomely from the Big Pharma buy-an-opinion system in which ‘thought leaders’ are lavishly remunerated via speaking fees and ‘consulting’ arrangements. Since 2016, he has received over US $1.6 million in pharma largesse.


    While McCullough’s declared pharma funding did decline during the peak years of Covidiocy, this was replaced with a lucrative new career of worldwide COVID speaking engagements and supplement sales. For a guy who was allegedly ‘cancelled,’ McCullough sure got a lot of coverage. Others like Michael Yeadon, the former Pfizer executive with the pelotas to come out and identify the poison prick campaign for what it really was - a mass homicide event predicated upon a non-existent virus - curiously got nowhere near the exposure enjoyed by McCullough (and fellow pandemic shills like Kirsch and Malone).

    McCullough enthusiastically pimps what he calls “The McCullough Protocol.” This protocol includes his highly-priced “Spike Support” supplement (US $64.99 for a 60-day supply) which contains the following substances (bold emphases added):

    Nattokinase (“a proteolytic enzyme with fibrinolytic (anti-clotting) effects, that may maintain a healthy immune system”)

    Dandelion root (“may support cellular defense”)

    Selenium (“may help reduce stress, aiding the body repair itself and recover”)

    Black sativa extract (“may facilitate cellular repair”)

    Green tea extract (“may add defenses at the cellular level through scavenging for free radicals”)

    Irish sea moss (“is mineral-rich and may help rebuild damaged tissue and muscle”)

    It’s hard to think of a flimsier basis for promoting this motley array of ingredients as a vaxxx detox formula. Using the same rationale for Irish sea moss (“is mineral-rich and may help rebuild damaged tissue and muscle”), one might as well recommend a thick, juicy steak as a “Spike” detox.

    None of these ingredients have been shown in anything resembling a controlled scientific study to help ameliorate post-vaxxxine injuries. Green tea extract, in fact, has a solid track record of causing liver toxicity and is a great supplement to avoid the hell out of - a woefully ignored issue I discuss in detail here.

    McCullough’s Recent Spike in Dubious Gene Therapy Claims

    On April 19, 2023, McCullough posted a brief Substack about a paper by Matthew Halma, Jessica Rose and Theresa Lawrie titled "The Novelty of mRNA Viral Vaccines and Potential Harms: A Scoping Review."

    McCullough repeated the paper’s title as headline for his own article, adding his own byline of “mRNA Off to a Bad Start but Future may be Brighter.”


    McCullough’s article employed the same “we must keep an open mind, remain balanced, and not paint issues with a broad brush” shtick that he employed in his hopelessly wrong statin article.

    I agree it’s good to keep an open mind - but not so open that your brains fall out.

    “The Halma paper,” claims McCullough, “points out that safe mRNA products are possible.”

    Here’s what the paper actually said:

    “If harm can be exclusively and conclusively attributed to the spike protein, then it is possible that future mRNA vaccines expressing other antigens will be safe.” (Bold emphasis added)

    McCullough apparently couldn’t find it within himself to neither highlight nor discuss the statement that immediately followed:

    “If harms are attributable to the platform itself, then regardless of the toxicity, or lack thereof, of the antigen to be expressed, the platform may be inherently unsafe, pending modification.” (Bold emphasis added)

    The McCullough interpretation makes it sound as if safe and effective mRNA drugs are just around the corner; what Halma et al wrote is a far more heavily qualified statement that speculates a possible scenario in which the drugs could be considered safe. If that specific condition isn’t met, they posit that the technology may be inherently dangerous, period.

    It’s rather precious to bang on about the importance of maintaining a balanced viewpoint while leaving that key detail out…

    So is mRNA technology inherently flawed, or is it a brilliant idea that just needs a few wrinkles ironed out before it starts saving millions of lives?

    After more than 30 years of research, mRNA technology failed to produce even a single, safe effective drug that made it through mandatory Phase 3 trials and garnered a New Drug Approval. Heck, none of this junk ever made it past the Phase 2 stage. The only reason the COVID gene therapies made it to market was thanks to the monumental scam known as COVID, which allowed the criminals in charge to declare a sniffles ‘emergency’ and rush the drugs through via the “Emergency Use Authorization” Trojan horse.

    The aftermath of the gene therapy rollout has been untold misery, morbidity and a global excess death toll estimated, at last count, between 18 and 35 million people. The kind of body count that would make Genghis Khan and Chairman Mao proud.

    To say mRNA is “Off to a Bad Start” is a monumental understatement.

    To say the future for mRNA technology may be brighter when that technology is still under the control of the same GloboPedo-Pharma-Military-Industrial Complex that bought us the COVID psy-op and Poison Prick democide fills me with about as much optimism as a family of crackheads moving in next door.

    Using Dodgy Novel Gene Therapies to Counter the Effects of Dodgy Novel Gene Therapies

    McCullough isn’t letting up on the idea that highly problematic gene therapies could be just what the doctor ordered.

    Recently, he and colleagues Nicolas Hulscher and Diane Marotta published a preprint titled “Strategic Deactivation of mRNA COVID-19 Vaccines: New Applications for RIBOTACs and siRNA Therapy.”

    According to McCullough, Hulscher and Marotta: "The rapid development and authorization of mRNA vaccines by Pfizer-BioNTech (BNT162b2) and Moderna (mRNA-1273) in 2020 marked a significant milestone in human mRNA product application, overcoming previous obstacles such as mRNA instability and immunogenicity."

    Let's be perfectly clear: The rapid development and authorization of mRNA vaccines was not a triumph over previous developmental obstacles, it was the triumph of untold evil and corruption over the traditional regulatory requirements and safeguards that are supposed to protect us against dangerous and ineffective drugs.

    It was a triumph over the last remnants of mainstream investigative reporting, whose practitioners have been almost entirely replaced by unthinking morons who’ll do and write whatever their Globalist-controlled employers tell them to.

    It was confirmation that the self-aggrandizing West is not a conglomerate of freedom-protecting democracies, but a centrally-controlled constellation of financially and/or sexually compromised politicians, bureaucrats and billionaire deviants who hold us in sheer contempt and not only wish to remove our freedoms but our very existence on this planet.


    A few sentences later, McCullough et al effectively acknowledge that obstacle-crushing mRNA technology isn’t so great after all, when they write:

    “The stability of mRNA vaccines, their pervasive distribution, and the longevity of the encapsulated mRNA along with unlimited production of the damaging and potentially lethal Spike (S) protein call for strategies to mitigate potential adverse effects.”

    In plain English: “The mRNA gene therapies are dangerous garbage that have caused untold illness and death. We need an effective strategy to treat the poor bastards who have been injected with this poison.”

    It seems McCullough’s Spike Support is about as effective as a fishnet condom, because nowhere in their paper do he and his co-authors discuss it as a potential remedy. Instead, the strategies they devote their paper to are gene therapies known as “small interfering RNA” (siRNA) and “ribonuclease targeting chimeras” (RIBOTACs).

    Yep, more synthetic RNA technology. Because we all know how well that worked out last time.

    These Brave New World genetic concoctions, posit the authors, may help counter the damage done by the small interfering psychopaths and “useless eater”-targeting Chimeras behind The Great Culling (in Greek mythology, the Chimera was a monstrous fire-breathing hybrid creature).

    Except McCullough et al don’t acknowledge The Great Culling, because they continue to regurgitate the insulting fairy tale that COVID was a genuine pandemic caused by the never-isolated and non-existent Sars-Cov-2.



    Some examples of highly toxic Australian and American fire-breathing Chimeras and small interfering psychopaths.
    Silencers: Not Just for Guns Anymore

    At this point you’re probably asking, “What the heck are siRNA and RIBOTACs?”

    Discovered in 1998, small interfering RNAs, sometimes known as short interfering RNAs or silencing RNAs, are noncoding RNAs with important roles in gene regulation.

    The initially double-stranded siRNA gets into cells, becomes part of what is dubbed the RNA-Induced Silencing Complex (RISC), and is unwound to form single stranded siRNA. It's now fit for duty to go out and find a complementary mRNA. Once the single stranded siRNA binds to its target mRNA, it induces mRNA cleavage.

    No, it doesn't give the mRNA a breast lift; "cleavage" in the world of science means to cut something up. Don't ask me why they don't just say that outright.

    Anyways, once the mRNA is cut, it is recognized as abnormal by the cell. The cell goes into garbage disposal mode and further degrades the mRNA, which prevents translation of the mRNA into amino acids and then proteins. This is what the gene "silencing" and “interfering” terminology refers to. Like a mafia informant who gets brutally shanked and can no longer talk to the feds, siRNA-sliced mRNA can no longer translate its encoded instructions into functioning proteins.

    Sorry, that was a somewhat gory analogy. You’ll have to excuse me, I'm back in Australia at the moment, a gray, soulless Masonic pit of substance abuse and mental illness that is run, policed and adjudicated by some of GloboPedo's most enthusiastically obedient deviants.

    But I digress.

    And RIBOTACs? What the hell are they?

    RIBOTACs are a new, man-made class of small molecules that have the potential to target diverse types of RNAs. In 2018, Scripps Institute researchers reported they were able to modify a small molecule to recruit a nuclease to a specific gene transcript, triggering its destruction.

    In plain English: Researchers continue to develop ‘novel’ ways to screw around with your genes.

    McCullough and co-authors speculate that it might be possible to develop siRNA and RIBOTAC gene therapies that will act as little vaxxx mRNA-munching Pacmen (or Pacpersons/PacTheys/PacThems/ma vaffanculo to all you anally-retentive, pronoun-confused PC-types).

    Sounds great, but there’s a wee problem.

    Warn the authors, "despite their numerous advantages, substantial obstacles must be surmounted to effectively harness the power of siRNAs. Barriers to the successful implementation of siRNAs as a therapeutic intervention include their susceptibility to degradation by endogenous nucleases in serum, rapid renal clearance, activation of the innate immune system, plasma protein sequestration and entrapment by the reticuloendothelial system (RES), membrane impermeability, endosomal entrapment and off-target effects."

    In inglés normal: This strategy is purely speculative and theoretical. There is no actual evidence siRNA and RIBOTACs can effectively treat vaxxx injuries. In fact, when you look at the research closely, there is no solid evidence these technologies can treat anything effectively. To top it all off, these technologies presently have numerous shortcomings that preclude their efficacy and may lead to "off-target effects", which is a polite way of saying nasty-ass side effects.

    As proof this fledgling technology could actually work, McCullough and co offer two examples of current siRNA drugs.

    Yup, this stuff is already appearing on the market thanks to the industry-funded shonks at the FDA.

    The first is Inclisiran (trade name Leqvio®) which has received FDA approval as a treatment for the utter non-disease of hypercholesterolemia. It’s very important to ‘treat’ this non-disease effectively, because studies repeatedly show that in over-60s (the demographic in which most heart attacks occur), people with high cholesterol levels (including the so-called “bad” LDL) outlive those with low levels.

    Did you forget there was a Great Culling going on?

    The authors write “seven clinical trials have shown this siRNA therapy to be safe and well-tolerated for long-term administration.” It allegedly did this in conflict of interest-riddled studies conducted by original developer Alnylam Pharmaceuticals and Novartis, which licensed the rights to inclisiran from the former.

    Mean duration of this "long-term administration" was 2.8 years. During that time, inclirisan completely failed to show any tangible clinical benefit.

    Even the hopelessly corrupt FDA, which approved this junk, quietly admits “The effect of Leqvio on cardiovascular morbidity (suffering from a disease) and mortality (death) has not been determined.”

    In other words, taking inclirisan means an increased risk of adverse drug effects and no established health benefit. The only people guaranteed to benefit from this product are those who sell it, at a cost of US $6,500 a year.

    Every single one of the 11 authors of the post hoc analysis McCullough and co cite as evidence of inclirisan being Safe & Effective™ have lengthy links to Big Pharma. Five, in fact, were employees of Novartis at the time the analysis was performed. All the authors enjoyed financial largesse from an array of drug companies that included … take a big deep breath … Novartis, Boehringer Ingelheim, The Medicines Company, AstraZeneca, Amgen, Pfizer, DalCor Pharmaceuticals, Kowa, Corvidia Therapeutics, Esperion, Genentech, OMEICOS, Novo Nordisk, LIB Therapeutics, Daiichi-Sankyo, New Amsterdam Pharma, TenSixteen Bio, Berlin-Chemie, Bristol Myers Squibb, Sanofi, Singulex, Abbott, Roche Diagnostics, Dr Beckmann Pharma, Bayer, HLS, Merck/Merck Sharp and Dohme, Aegerion Pharmaceuticals, Cipla, Algorithm, Zuelling Pharma, Regeneron Pharmaceuticals, Eli Lilly, Cerenis Therapeutics, Akcea Therapeutics, Silence Therapeutics, Takeda, AbbVie and Resverlogix.

    In addition, one of the authors, Gregory G. Schwartz, is co-holder of a patent titled "Methods for Reducing Cardiovascular Risk." The patent revolves around the monoclonal antibody drug alirocumab which, like inclirisan, is a cholesterol-lowering drug whose mechanism of action is inhibition of a gene known as PCSK9.

    Like inclirisan, alirocumab does not save lives but comes with all the usual side effects attendant with cholesterol-lowering.

    Like inclirisan, alicrocumab is an out-and-out rort. When alirocumab and fellow useless PCSK9 inhibitor evolocumab hit the market in 2015, the retail cost was an absurd $14,000 per year. After many health insurance providers refused to pay for them, their price tag magically dropped by 60%.

    The amount of trust I have in such a conflict of interest-plagued panel of pharma-owned researchers when they claim the ineffective inclirisan is “safe and well-tolerated”?

    Absolute zero.

    Indeed, when you pull up the Supplementary Material and scroll down to page 23, you quickly learn why the all-cause mortality figure wasn’t included in the analysis’ main paper.

    During a mean exposure period of 2.8 years, 24 (0.7%) of inclirisan subjects died, compared to 3 (0.2%) of placebo subjects during an average exposure period of 1.35 years. When calculated in terms of "exposure-adjusted incidence rates," the death rates in the inclirisan and placebo groups were 0.24% and 0.11%, respectively.

    In other words, the "safe and well-tolerated" inclirisan more than doubled the death rate when compared to placebo.

    Patisiran Poppycock

    The other drug that McCullough et al put forward as an example of "safe and well-tolerated" siRNA treatment is patisiran (Onpattro®), which received FDA approval in 2018 for the treatment of polyneuropathy in patients with hereditary transthyretin-mediated amyloidosis.

    Just like inclirisan, the clinical evidence supposedly showing this drug to be hunky dory is the same old suspicious rot produced by the hopelessly flawed and demonstrably corrupt system in which drug companies conduct their own trials, get approval from their FDA buddies, pay ghost-writing outfits to draft the application and journal papers, while the rest of us are supposed to stick our heads up our keesters and pretend the drug really was shown to be safe and efficacious.

    The first published Phase 3 trial claiming safety and efficacy for patisiran appeared in the New World Order England Journal of Medicine in July 2018.

    In that paper, Adams et al reported the initial results of the “APOLLO” trial which, of course, was funded by Alnylam Pharmaceuticals. The study's lead author is David Adams, who has received "consulting honoraria from Isis, Alnylam, received fees from Pfizer for participating to symposium, is participating as principal investigator for trials with ISIS and Alnylam."

    We learn from the paper’s full text that “The first author and sponsor-employed authors prepared the first draft with editorial assistance provided by Adelphi Communications, under contract with Alnylam Pharmaceuticals.”

    Adelphi Communications is one of the countless “communication” outfits contracted by drug companies that do everything from oversee the recruitment and day-to-day operation of clinical trials to ghost-writing journal papers. Like most businesses in the private sector, the success of these companies revolves around pleasing their customers. The way to please drug companies is not by telling the truth about their dangerous and toxic products - it is by chopping and changing the data and writing up journal papers in a manner that portrays these products as safe and effective.

    A close read of the paper raises eyebrows.

    Partirisan, claim the authors, fared better than placebo on every outcome.

    The researchers also claim the incidence of “any adverse event” was identical between groups (97% each). They also claimed a lower rate of adverse cardiovascular events in the partirisan group. Hold that thought - we’ll return to it later.

    The most important outcome of all is overall mortality. The researchers report that seven patisiran patients (5%) and six placebo patients (8%) died during the 18-month trial.

    In 2020, the APOLLO researchers published another paper reporting on the 225 subjects randomized to receive either patisiran or placebo. In this paper, we are told 6 (4%) patisiran subjects died at 18 months, compared to 4 (5%) of placebo subjects.

    In 2022, researchers published results from the HELIOS-A trial. The randomized, Phase 3, open-label (non-blinded) study enrolled 164 patients; 42 received patisiran, 77 served as a control subjects, and 122 received Alnylam's new wonder siRNA concoction called vutrisiran.

    By way of remarkable coincidence, patisiran now displayed a near-identical death rate to placebo (7.1% vs 7.8%), and a marginally higher rate of serious and severe adverse events. By way of further remarkable coincidence, the new viturisan with its fresher patent protection produced a mere 1.6% death rate and a far lower rate of adverse events.

    Amazing.

    Or complete bollocks, depending on how schooled you are in the conduct of Big Pharma and the researchers it owns.

    In 2023, the results of the Alnylam-funded "APOLLO-B" trial were published. The main paper states that in the 12-month double-blind period, 4 deaths (2.2%) occurred in the patisiran group and 10 (5.6%) occurred in the placebo group.

    It then goes on to say that in the "safety analysis," there were five deaths (3%) in the patisiran group, and eight deaths (4%) in the placebo group.

    Seeking an explanation for these disparate figures, I opened up the trial's supplementary data. It was there I learned that in the patisiran group, four patients died during participation in the study and one died after withdrawing from the study. In the placebo group, four patients died during participation in the study and four died after study withdrawal.

    In other words, an equal number of patisiran and placebo subjects died while participating in the APOLLO-B trial.

    We also learn in the supplementary material that "Hospitalizations for any cause" were virtually identical in the two groups. In contrast to the original APOLLO trial, marginally higher rates of cardiac and cerebrovascular events occurred in the patisiran group.

    In summary, the only data claiming patisiran (and vutrisiran) benefits transthyretin amyloidosis patients just happens to come from trials conducted by the drug’s developer, Alnylam Pharmaceuticals, and the pharma-friendly researchers on its payroll. The suspect data from these trials fails to show any clear mortality benefit, which makes one wonder what the death data would’ve looked like had the trials been conducted by independent researchers with no vested interest in the results.

    Useless inclirisan and doubtful patisiran, it bears reiterating, are the two drugs put forward by McCullough et al as successful examples of siRNA technology.

    Lipid Nanopoison

    Now here’s the real cracker.

    Patisiran, which McCullough et al present as an example of a “safe and well-tolerated” siRNA product, contains lipid nanoparticles (LNPs).

    As do the most widely-deployed COVID gene therapies; namely, the Pfizer and Moderna kill shots.

    McCullough, you will recall, has made a lucrative name for himself as a staunch anti-mRNA vaxxx commentator. After reading the paper he co-authored with Hulscher and Marotta, I began to wonder if he suffered transient global amnesia (a known statin side effect) when drafting the paper.

    That paper lavishes praise upon LNPs and how they admirably transformed the useless and dangerous gene therapies that failed to garner approval into useless and dangerous gene therapies that garnered emergency use authorizations. Okay, that’s not exactly how they described it, but that’s exactly what happened.

    Their incessant praise of LNPs as an “adjuvant” that could help do the same for vaxxxMRNA-gobbling siRNA drugs is nothing short of mind-boggling.

    “Adjuvant,” by the way, is ScienceSpeak for a toxic substance disguised as an ingredient that allegedly improves the ‘immunogenicity’ of a vaccine. Anyone who believes injecting people with stuff like thimerosal, squalene or polyethylene glycol is truly going to benefit their immunity should probably start shopping around for a brain transplant.

    Way back in December 2020, within a week of the Pfizer kill shot being unleashed in the US, the LNP polyethylene glycol (PEG) was named as a likely cause of life-threatening anaphylaxis that occurred after injection with the democide drug.

    The issue, of course, has been swept under the carpet and PEG remains in the poison darts. As researchers recently pointed out, no studies have been undertaken to characterize the inflammatory reactions induced by the PEG-containing 'vaccine' platform. So the researchers tested a lipid nanoparticle formula made by Acuitas Therapeutics, who licenses its LNP technology to Pfizer.

    They gave mice the Acuitas poison formula, via intradermal and intramuscular injection, which "led to rapid and robust inflammatory responses, characterized by massive neutrophil infiltration, activation of diverse inflammatory pathways, and production of various inflammatory cytokines and chemokines."

    In Queen's English: This most questionable substance caused these most unfortunate mice an inordinate amount of physiological bother.

    In fact, when the mice were forced to ingest this junk via their snouts, they experienced an inordinate amount of death.

    "The same dose of LNP delivered intranasally," noted the researchers, "led to similar inflammatory responses in the lung and resulted in a high mortality rate."

    Coming soon: Intranasal vaccines with extra-strength LNP, brought to you by the friendly megalomaniacs at GloboPedo!

    In Summary

    For a guy who supposedly wants you to be healthy, Peter McCullough has a bizarre habit of recommending toxic pharma junk and awarding praise to dubious gene therapies that are light years away from proving themselves safe and effective.

    There are two possible reasons for this.

    One is that he is not very good at reading research and, like many doctors and cardiologists, is simply a brainwashed product of the pharma-owned and -operated medical system.

    The other possibility is that he is controlled opposition carefully packaged to look like your respectable Uncle Ronald. Instead of calling out the pandemic scam, he in fact helps pave the way for future shamdemics and shambolic gene therapy rollouts by proffering favourable and optimistic commentary on what has so far proven to be a truly nefarious and dangerous field of ‘science.’

    For McCullough devotees offended that I dare mention the second possibility, I have this piece of advice: If you don’t want McCullough to be perceived as a possible controlled opposition figure, maybe ask him to stop acting like one.

    In the meantime, Mike Yeadon for President! Oh, wait, he’s from the UK. Damnit America, looks like you’re stuck with either Captain Warp Speed or Joe the Kiddy Fondler. As citizen of a country currently led by a vewy angwee* pwime minista who has been known to frequent Thai “Happy Ending” massage parlours to rewieve the stwess of fedwal powitics, I feel your pain.

    *PM Elmer Fudd is still vewy angwee dat wascawwy Austwalians voted ovawelmingwee against his pawly expwained “Voice” wefewendum. PM Fudd had a wot widing on dat wefewendum, and his land-gwabbing gwobawist masters are vewy upset dat it fayled.

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    https://substack.com/home/post/p-145590321
    Dr Peter McCullough Recommends Dodgey Synthetic siRNA Jabs to Counter Effects of Dodgey Synthetic mRNA Jabs You're in great hands, health freedom movement! Not. Anthony Colpo The Medical Freedom Movement is full of suspicious characters. So suspicious you'd almost think the movement has been captured, or even commandeered from the outset, by the same people who brought us the 2020 blockbuster "The Great Culling: This Time, it’s Global!” There's Steve Kirsch, the DARPA teen protege and Rockefeller-linked buffoon famous for The Most Important Surveys You'll Ever Do!!, big money challenges he has no intention of fulfilling, surveillance state and CBDC technology, and aggressive promotion of the highly toxic, suicide-inducing SSRI fluvoxamine. There's Robert "Sly" Malone, the self-proclaimed inventor of "mRNA vaccine technology" who cries hard-done-by while swimming around in billion$ of grant money from the US Military (major enablers of the globalist death shot campaign), all while pretending claiming to be an injured vaxxx victim. There's Brett Weinstein, who helped propel Kirsch and Malone into stardom with his June 11, 2021 Darkhorse Podcast. In this creepy snippet from his Tucker Carlson interview, Weinstein gushes like a lovesick teen over mRNA technology. Such impassioned praise for a technology with a 30-year track record of failure, one that was successfully deployed to trigger accelerated death and disability around the world, is extremely curious for someone presenting as a health freedom fighter. There's Dr Ryan Cole who, at "the first Conversation on Covid" in Puerto Rico September 2021, emphatically emphasized “Covid is a clotting disease. Covid is a clotting disease. Covid is a clotting disease.” In case you didn't catch it the first three times, Cole reckons COVID is a clotting disease. Bollocks. COVID is regular cold, flu and pneumonia renamed and packaged as an uber-deadly new threat. They are not "clotting diseases" but respiratory ailments. What is a clotting disease is the common and now well-documented life-threatening thrombosis caused by the Unsafe and Ineffective gene therapies to treat the renamed COVID caused by the never-isolated Sars-Cov-2. Despite this clotting effect of the vaxxxines being well-established by September 2021, Cole preferred to blame the phenomenon on 'COVID.' With health freedom heroes like this, who needs villains? The “remarkable” San Juan “Covid Conversation” where health freedom spokespeople not chosen by you acted as if COVID was real and not a globalist psy-op. There's Dr Pierre Kory who, at the same star-studded gathering of pandemic shills, described COVID, the artist formerly known as Cold’n’Flu, as "the most complex and most violent disease that I have seen and the most difficult to treat in the ICU.” COVID: Once a simple cold you sat out with some hot tea, lemon juice and Vaporub, now the most complex and violent thug of a disease the world of medicine has ever seen! If the madicine gig ever stops working out for Kory, he should migrate to Australia and get a job as a SAPOL prosecutor - with such an unbridled capacity for egregious nonsense, he'd fit right in. Dr Pierre Kory, supposed member of the Health Freedom Movement, pushing the mask farce in uber-mainstream USA Today. The ‘Respectable’ Face of Pandemic and Gene Therapy Propaganda? Then there's the movement's smiling enigma, Dr Peter McCullough. Depending on who you listen to, McCullough is either a controlled opposition shill or the most sincere bloke you could ever meet. Compared to some of the other suspect characters who comprise the upper echelons of the health freedom movement, there's something disarming about McCullough. He doesn't have the grating motor mouth of Kirsch, nor the sinister gaze and evil gnome vibe of Malone. McCullough appears the polar opposite of Kirsch, who comes off like the tech-nerd version of your obnoxious, balding, know-it-all Uncle Barry. The guy who slurps, farts, belches at family gatherings and blames it on the dog, and challenges his nephews to wrestling matches while drunk then refuses to concede defeat when they repeatedly pin his fat hairy shoulders to the ground. McCullough seems more like your Uncle Ronald, the successful physician who arrives at family gatherings with your charmingly demure and well-liked Auntie Mary in his late model Jaguar. He doesn't act like a bogan, doesn't antagonize his nephews, and generally presents as a jovial, amicable, clean-living guy. But from behind McCullough's disarming facade there emanates some very dubious claims. I started to smell the pungent odour of pharma-sponsored allopathic bullpoop, extra-strength version, when McCullough claimed toxic statin drugs reduced the risk of dementia and Alzheimers Disease. Anyone who even pretends to care about health and medical freedom has no business praising toxic and ineffective garbage like cholesterol-lowering statins. To make his claim, McCullough had to ignore the substantial volume of clinical trial evidence showing both low cholesterol and cholesterol reduction via statins not only fail to prevent dementia and Alzheimers Disease, but often result in cognitive and neurological harms. Cholesterol is an integral component of your brain and nerve sheaths - claiming you can prevent cognitive and neurological decline by lowering cholesterol is like claiming your car will drive further and longer after you drain half the fuel from the tank. It is an inherently absurd and false thing to claim. McCullough, however, appears to have no issue with making inherently absurd and false claims. Because the RCT evidence wouldn't support his beloved statins, he instead based his untenable claims entirely upon a a 2022 meta-analysis of epidemiological studies by Italian researchers - two of whom have extensive ties to pharma companies, including cholesterol-lowering drug manufacturers like Pfizer, Merck, Amgen, Servier and Sanofi-Regeneron. Just brilliant. No matter how you wish to frame it, McCullough has benefited handsomely from the Big Pharma buy-an-opinion system in which ‘thought leaders’ are lavishly remunerated via speaking fees and ‘consulting’ arrangements. Since 2016, he has received over US $1.6 million in pharma largesse. While McCullough’s declared pharma funding did decline during the peak years of Covidiocy, this was replaced with a lucrative new career of worldwide COVID speaking engagements and supplement sales. For a guy who was allegedly ‘cancelled,’ McCullough sure got a lot of coverage. Others like Michael Yeadon, the former Pfizer executive with the pelotas to come out and identify the poison prick campaign for what it really was - a mass homicide event predicated upon a non-existent virus - curiously got nowhere near the exposure enjoyed by McCullough (and fellow pandemic shills like Kirsch and Malone). McCullough enthusiastically pimps what he calls “The McCullough Protocol.” This protocol includes his highly-priced “Spike Support” supplement (US $64.99 for a 60-day supply) which contains the following substances (bold emphases added): Nattokinase (“a proteolytic enzyme with fibrinolytic (anti-clotting) effects, that may maintain a healthy immune system”) Dandelion root (“may support cellular defense”) Selenium (“may help reduce stress, aiding the body repair itself and recover”) Black sativa extract (“may facilitate cellular repair”) Green tea extract (“may add defenses at the cellular level through scavenging for free radicals”) Irish sea moss (“is mineral-rich and may help rebuild damaged tissue and muscle”) It’s hard to think of a flimsier basis for promoting this motley array of ingredients as a vaxxx detox formula. Using the same rationale for Irish sea moss (“is mineral-rich and may help rebuild damaged tissue and muscle”), one might as well recommend a thick, juicy steak as a “Spike” detox. None of these ingredients have been shown in anything resembling a controlled scientific study to help ameliorate post-vaxxxine injuries. Green tea extract, in fact, has a solid track record of causing liver toxicity and is a great supplement to avoid the hell out of - a woefully ignored issue I discuss in detail here. McCullough’s Recent Spike in Dubious Gene Therapy Claims On April 19, 2023, McCullough posted a brief Substack about a paper by Matthew Halma, Jessica Rose and Theresa Lawrie titled "The Novelty of mRNA Viral Vaccines and Potential Harms: A Scoping Review." McCullough repeated the paper’s title as headline for his own article, adding his own byline of “mRNA Off to a Bad Start but Future may be Brighter.” McCullough’s article employed the same “we must keep an open mind, remain balanced, and not paint issues with a broad brush” shtick that he employed in his hopelessly wrong statin article. I agree it’s good to keep an open mind - but not so open that your brains fall out. “The Halma paper,” claims McCullough, “points out that safe mRNA products are possible.” Here’s what the paper actually said: “If harm can be exclusively and conclusively attributed to the spike protein, then it is possible that future mRNA vaccines expressing other antigens will be safe.” (Bold emphasis added) McCullough apparently couldn’t find it within himself to neither highlight nor discuss the statement that immediately followed: “If harms are attributable to the platform itself, then regardless of the toxicity, or lack thereof, of the antigen to be expressed, the platform may be inherently unsafe, pending modification.” (Bold emphasis added) The McCullough interpretation makes it sound as if safe and effective mRNA drugs are just around the corner; what Halma et al wrote is a far more heavily qualified statement that speculates a possible scenario in which the drugs could be considered safe. If that specific condition isn’t met, they posit that the technology may be inherently dangerous, period. It’s rather precious to bang on about the importance of maintaining a balanced viewpoint while leaving that key detail out… So is mRNA technology inherently flawed, or is it a brilliant idea that just needs a few wrinkles ironed out before it starts saving millions of lives? After more than 30 years of research, mRNA technology failed to produce even a single, safe effective drug that made it through mandatory Phase 3 trials and garnered a New Drug Approval. Heck, none of this junk ever made it past the Phase 2 stage. The only reason the COVID gene therapies made it to market was thanks to the monumental scam known as COVID, which allowed the criminals in charge to declare a sniffles ‘emergency’ and rush the drugs through via the “Emergency Use Authorization” Trojan horse. The aftermath of the gene therapy rollout has been untold misery, morbidity and a global excess death toll estimated, at last count, between 18 and 35 million people. The kind of body count that would make Genghis Khan and Chairman Mao proud. To say mRNA is “Off to a Bad Start” is a monumental understatement. To say the future for mRNA technology may be brighter when that technology is still under the control of the same GloboPedo-Pharma-Military-Industrial Complex that bought us the COVID psy-op and Poison Prick democide fills me with about as much optimism as a family of crackheads moving in next door. Using Dodgy Novel Gene Therapies to Counter the Effects of Dodgy Novel Gene Therapies McCullough isn’t letting up on the idea that highly problematic gene therapies could be just what the doctor ordered. Recently, he and colleagues Nicolas Hulscher and Diane Marotta published a preprint titled “Strategic Deactivation of mRNA COVID-19 Vaccines: New Applications for RIBOTACs and siRNA Therapy.” According to McCullough, Hulscher and Marotta: "The rapid development and authorization of mRNA vaccines by Pfizer-BioNTech (BNT162b2) and Moderna (mRNA-1273) in 2020 marked a significant milestone in human mRNA product application, overcoming previous obstacles such as mRNA instability and immunogenicity." Let's be perfectly clear: The rapid development and authorization of mRNA vaccines was not a triumph over previous developmental obstacles, it was the triumph of untold evil and corruption over the traditional regulatory requirements and safeguards that are supposed to protect us against dangerous and ineffective drugs. It was a triumph over the last remnants of mainstream investigative reporting, whose practitioners have been almost entirely replaced by unthinking morons who’ll do and write whatever their Globalist-controlled employers tell them to. It was confirmation that the self-aggrandizing West is not a conglomerate of freedom-protecting democracies, but a centrally-controlled constellation of financially and/or sexually compromised politicians, bureaucrats and billionaire deviants who hold us in sheer contempt and not only wish to remove our freedoms but our very existence on this planet. A few sentences later, McCullough et al effectively acknowledge that obstacle-crushing mRNA technology isn’t so great after all, when they write: “The stability of mRNA vaccines, their pervasive distribution, and the longevity of the encapsulated mRNA along with unlimited production of the damaging and potentially lethal Spike (S) protein call for strategies to mitigate potential adverse effects.” In plain English: “The mRNA gene therapies are dangerous garbage that have caused untold illness and death. We need an effective strategy to treat the poor bastards who have been injected with this poison.” It seems McCullough’s Spike Support is about as effective as a fishnet condom, because nowhere in their paper do he and his co-authors discuss it as a potential remedy. Instead, the strategies they devote their paper to are gene therapies known as “small interfering RNA” (siRNA) and “ribonuclease targeting chimeras” (RIBOTACs). Yep, more synthetic RNA technology. Because we all know how well that worked out last time. These Brave New World genetic concoctions, posit the authors, may help counter the damage done by the small interfering psychopaths and “useless eater”-targeting Chimeras behind The Great Culling (in Greek mythology, the Chimera was a monstrous fire-breathing hybrid creature). Except McCullough et al don’t acknowledge The Great Culling, because they continue to regurgitate the insulting fairy tale that COVID was a genuine pandemic caused by the never-isolated and non-existent Sars-Cov-2. Some examples of highly toxic Australian and American fire-breathing Chimeras and small interfering psychopaths. Silencers: Not Just for Guns Anymore At this point you’re probably asking, “What the heck are siRNA and RIBOTACs?” Discovered in 1998, small interfering RNAs, sometimes known as short interfering RNAs or silencing RNAs, are noncoding RNAs with important roles in gene regulation. The initially double-stranded siRNA gets into cells, becomes part of what is dubbed the RNA-Induced Silencing Complex (RISC), and is unwound to form single stranded siRNA. It's now fit for duty to go out and find a complementary mRNA. Once the single stranded siRNA binds to its target mRNA, it induces mRNA cleavage. No, it doesn't give the mRNA a breast lift; "cleavage" in the world of science means to cut something up. Don't ask me why they don't just say that outright. Anyways, once the mRNA is cut, it is recognized as abnormal by the cell. The cell goes into garbage disposal mode and further degrades the mRNA, which prevents translation of the mRNA into amino acids and then proteins. This is what the gene "silencing" and “interfering” terminology refers to. Like a mafia informant who gets brutally shanked and can no longer talk to the feds, siRNA-sliced mRNA can no longer translate its encoded instructions into functioning proteins. Sorry, that was a somewhat gory analogy. You’ll have to excuse me, I'm back in Australia at the moment, a gray, soulless Masonic pit of substance abuse and mental illness that is run, policed and adjudicated by some of GloboPedo's most enthusiastically obedient deviants. But I digress. And RIBOTACs? What the hell are they? RIBOTACs are a new, man-made class of small molecules that have the potential to target diverse types of RNAs. In 2018, Scripps Institute researchers reported they were able to modify a small molecule to recruit a nuclease to a specific gene transcript, triggering its destruction. In plain English: Researchers continue to develop ‘novel’ ways to screw around with your genes. McCullough and co-authors speculate that it might be possible to develop siRNA and RIBOTAC gene therapies that will act as little vaxxx mRNA-munching Pacmen (or Pacpersons/PacTheys/PacThems/ma vaffanculo to all you anally-retentive, pronoun-confused PC-types). Sounds great, but there’s a wee problem. Warn the authors, "despite their numerous advantages, substantial obstacles must be surmounted to effectively harness the power of siRNAs. Barriers to the successful implementation of siRNAs as a therapeutic intervention include their susceptibility to degradation by endogenous nucleases in serum, rapid renal clearance, activation of the innate immune system, plasma protein sequestration and entrapment by the reticuloendothelial system (RES), membrane impermeability, endosomal entrapment and off-target effects." In inglés normal: This strategy is purely speculative and theoretical. There is no actual evidence siRNA and RIBOTACs can effectively treat vaxxx injuries. In fact, when you look at the research closely, there is no solid evidence these technologies can treat anything effectively. To top it all off, these technologies presently have numerous shortcomings that preclude their efficacy and may lead to "off-target effects", which is a polite way of saying nasty-ass side effects. As proof this fledgling technology could actually work, McCullough and co offer two examples of current siRNA drugs. Yup, this stuff is already appearing on the market thanks to the industry-funded shonks at the FDA. The first is Inclisiran (trade name Leqvio®) which has received FDA approval as a treatment for the utter non-disease of hypercholesterolemia. It’s very important to ‘treat’ this non-disease effectively, because studies repeatedly show that in over-60s (the demographic in which most heart attacks occur), people with high cholesterol levels (including the so-called “bad” LDL) outlive those with low levels. Did you forget there was a Great Culling going on? The authors write “seven clinical trials have shown this siRNA therapy to be safe and well-tolerated for long-term administration.” It allegedly did this in conflict of interest-riddled studies conducted by original developer Alnylam Pharmaceuticals and Novartis, which licensed the rights to inclisiran from the former. Mean duration of this "long-term administration" was 2.8 years. During that time, inclirisan completely failed to show any tangible clinical benefit. Even the hopelessly corrupt FDA, which approved this junk, quietly admits “The effect of Leqvio on cardiovascular morbidity (suffering from a disease) and mortality (death) has not been determined.” In other words, taking inclirisan means an increased risk of adverse drug effects and no established health benefit. The only people guaranteed to benefit from this product are those who sell it, at a cost of US $6,500 a year. Every single one of the 11 authors of the post hoc analysis McCullough and co cite as evidence of inclirisan being Safe & Effective™ have lengthy links to Big Pharma. Five, in fact, were employees of Novartis at the time the analysis was performed. All the authors enjoyed financial largesse from an array of drug companies that included … take a big deep breath … Novartis, Boehringer Ingelheim, The Medicines Company, AstraZeneca, Amgen, Pfizer, DalCor Pharmaceuticals, Kowa, Corvidia Therapeutics, Esperion, Genentech, OMEICOS, Novo Nordisk, LIB Therapeutics, Daiichi-Sankyo, New Amsterdam Pharma, TenSixteen Bio, Berlin-Chemie, Bristol Myers Squibb, Sanofi, Singulex, Abbott, Roche Diagnostics, Dr Beckmann Pharma, Bayer, HLS, Merck/Merck Sharp and Dohme, Aegerion Pharmaceuticals, Cipla, Algorithm, Zuelling Pharma, Regeneron Pharmaceuticals, Eli Lilly, Cerenis Therapeutics, Akcea Therapeutics, Silence Therapeutics, Takeda, AbbVie and Resverlogix. In addition, one of the authors, Gregory G. Schwartz, is co-holder of a patent titled "Methods for Reducing Cardiovascular Risk." The patent revolves around the monoclonal antibody drug alirocumab which, like inclirisan, is a cholesterol-lowering drug whose mechanism of action is inhibition of a gene known as PCSK9. Like inclirisan, alirocumab does not save lives but comes with all the usual side effects attendant with cholesterol-lowering. Like inclirisan, alicrocumab is an out-and-out rort. When alirocumab and fellow useless PCSK9 inhibitor evolocumab hit the market in 2015, the retail cost was an absurd $14,000 per year. After many health insurance providers refused to pay for them, their price tag magically dropped by 60%. The amount of trust I have in such a conflict of interest-plagued panel of pharma-owned researchers when they claim the ineffective inclirisan is “safe and well-tolerated”? Absolute zero. Indeed, when you pull up the Supplementary Material and scroll down to page 23, you quickly learn why the all-cause mortality figure wasn’t included in the analysis’ main paper. During a mean exposure period of 2.8 years, 24 (0.7%) of inclirisan subjects died, compared to 3 (0.2%) of placebo subjects during an average exposure period of 1.35 years. When calculated in terms of "exposure-adjusted incidence rates," the death rates in the inclirisan and placebo groups were 0.24% and 0.11%, respectively. In other words, the "safe and well-tolerated" inclirisan more than doubled the death rate when compared to placebo. Patisiran Poppycock The other drug that McCullough et al put forward as an example of "safe and well-tolerated" siRNA treatment is patisiran (Onpattro®), which received FDA approval in 2018 for the treatment of polyneuropathy in patients with hereditary transthyretin-mediated amyloidosis. Just like inclirisan, the clinical evidence supposedly showing this drug to be hunky dory is the same old suspicious rot produced by the hopelessly flawed and demonstrably corrupt system in which drug companies conduct their own trials, get approval from their FDA buddies, pay ghost-writing outfits to draft the application and journal papers, while the rest of us are supposed to stick our heads up our keesters and pretend the drug really was shown to be safe and efficacious. The first published Phase 3 trial claiming safety and efficacy for patisiran appeared in the New World Order England Journal of Medicine in July 2018. In that paper, Adams et al reported the initial results of the “APOLLO” trial which, of course, was funded by Alnylam Pharmaceuticals. The study's lead author is David Adams, who has received "consulting honoraria from Isis, Alnylam, received fees from Pfizer for participating to symposium, is participating as principal investigator for trials with ISIS and Alnylam." We learn from the paper’s full text that “The first author and sponsor-employed authors prepared the first draft with editorial assistance provided by Adelphi Communications, under contract with Alnylam Pharmaceuticals.” Adelphi Communications is one of the countless “communication” outfits contracted by drug companies that do everything from oversee the recruitment and day-to-day operation of clinical trials to ghost-writing journal papers. Like most businesses in the private sector, the success of these companies revolves around pleasing their customers. The way to please drug companies is not by telling the truth about their dangerous and toxic products - it is by chopping and changing the data and writing up journal papers in a manner that portrays these products as safe and effective. A close read of the paper raises eyebrows. Partirisan, claim the authors, fared better than placebo on every outcome. The researchers also claim the incidence of “any adverse event” was identical between groups (97% each). They also claimed a lower rate of adverse cardiovascular events in the partirisan group. Hold that thought - we’ll return to it later. The most important outcome of all is overall mortality. The researchers report that seven patisiran patients (5%) and six placebo patients (8%) died during the 18-month trial. In 2020, the APOLLO researchers published another paper reporting on the 225 subjects randomized to receive either patisiran or placebo. In this paper, we are told 6 (4%) patisiran subjects died at 18 months, compared to 4 (5%) of placebo subjects. In 2022, researchers published results from the HELIOS-A trial. The randomized, Phase 3, open-label (non-blinded) study enrolled 164 patients; 42 received patisiran, 77 served as a control subjects, and 122 received Alnylam's new wonder siRNA concoction called vutrisiran. By way of remarkable coincidence, patisiran now displayed a near-identical death rate to placebo (7.1% vs 7.8%), and a marginally higher rate of serious and severe adverse events. By way of further remarkable coincidence, the new viturisan with its fresher patent protection produced a mere 1.6% death rate and a far lower rate of adverse events. Amazing. Or complete bollocks, depending on how schooled you are in the conduct of Big Pharma and the researchers it owns. In 2023, the results of the Alnylam-funded "APOLLO-B" trial were published. The main paper states that in the 12-month double-blind period, 4 deaths (2.2%) occurred in the patisiran group and 10 (5.6%) occurred in the placebo group. It then goes on to say that in the "safety analysis," there were five deaths (3%) in the patisiran group, and eight deaths (4%) in the placebo group. Seeking an explanation for these disparate figures, I opened up the trial's supplementary data. It was there I learned that in the patisiran group, four patients died during participation in the study and one died after withdrawing from the study. In the placebo group, four patients died during participation in the study and four died after study withdrawal. In other words, an equal number of patisiran and placebo subjects died while participating in the APOLLO-B trial. We also learn in the supplementary material that "Hospitalizations for any cause" were virtually identical in the two groups. In contrast to the original APOLLO trial, marginally higher rates of cardiac and cerebrovascular events occurred in the patisiran group. In summary, the only data claiming patisiran (and vutrisiran) benefits transthyretin amyloidosis patients just happens to come from trials conducted by the drug’s developer, Alnylam Pharmaceuticals, and the pharma-friendly researchers on its payroll. The suspect data from these trials fails to show any clear mortality benefit, which makes one wonder what the death data would’ve looked like had the trials been conducted by independent researchers with no vested interest in the results. Useless inclirisan and doubtful patisiran, it bears reiterating, are the two drugs put forward by McCullough et al as successful examples of siRNA technology. Lipid Nanopoison Now here’s the real cracker. Patisiran, which McCullough et al present as an example of a “safe and well-tolerated” siRNA product, contains lipid nanoparticles (LNPs). As do the most widely-deployed COVID gene therapies; namely, the Pfizer and Moderna kill shots. McCullough, you will recall, has made a lucrative name for himself as a staunch anti-mRNA vaxxx commentator. After reading the paper he co-authored with Hulscher and Marotta, I began to wonder if he suffered transient global amnesia (a known statin side effect) when drafting the paper. That paper lavishes praise upon LNPs and how they admirably transformed the useless and dangerous gene therapies that failed to garner approval into useless and dangerous gene therapies that garnered emergency use authorizations. Okay, that’s not exactly how they described it, but that’s exactly what happened. Their incessant praise of LNPs as an “adjuvant” that could help do the same for vaxxxMRNA-gobbling siRNA drugs is nothing short of mind-boggling. “Adjuvant,” by the way, is ScienceSpeak for a toxic substance disguised as an ingredient that allegedly improves the ‘immunogenicity’ of a vaccine. Anyone who believes injecting people with stuff like thimerosal, squalene or polyethylene glycol is truly going to benefit their immunity should probably start shopping around for a brain transplant. Way back in December 2020, within a week of the Pfizer kill shot being unleashed in the US, the LNP polyethylene glycol (PEG) was named as a likely cause of life-threatening anaphylaxis that occurred after injection with the democide drug. The issue, of course, has been swept under the carpet and PEG remains in the poison darts. As researchers recently pointed out, no studies have been undertaken to characterize the inflammatory reactions induced by the PEG-containing 'vaccine' platform. So the researchers tested a lipid nanoparticle formula made by Acuitas Therapeutics, who licenses its LNP technology to Pfizer. They gave mice the Acuitas poison formula, via intradermal and intramuscular injection, which "led to rapid and robust inflammatory responses, characterized by massive neutrophil infiltration, activation of diverse inflammatory pathways, and production of various inflammatory cytokines and chemokines." In Queen's English: This most questionable substance caused these most unfortunate mice an inordinate amount of physiological bother. In fact, when the mice were forced to ingest this junk via their snouts, they experienced an inordinate amount of death. "The same dose of LNP delivered intranasally," noted the researchers, "led to similar inflammatory responses in the lung and resulted in a high mortality rate." Coming soon: Intranasal vaccines with extra-strength LNP, brought to you by the friendly megalomaniacs at GloboPedo! In Summary For a guy who supposedly wants you to be healthy, Peter McCullough has a bizarre habit of recommending toxic pharma junk and awarding praise to dubious gene therapies that are light years away from proving themselves safe and effective. There are two possible reasons for this. One is that he is not very good at reading research and, like many doctors and cardiologists, is simply a brainwashed product of the pharma-owned and -operated medical system. The other possibility is that he is controlled opposition carefully packaged to look like your respectable Uncle Ronald. Instead of calling out the pandemic scam, he in fact helps pave the way for future shamdemics and shambolic gene therapy rollouts by proffering favourable and optimistic commentary on what has so far proven to be a truly nefarious and dangerous field of ‘science.’ For McCullough devotees offended that I dare mention the second possibility, I have this piece of advice: If you don’t want McCullough to be perceived as a possible controlled opposition figure, maybe ask him to stop acting like one. In the meantime, Mike Yeadon for President! Oh, wait, he’s from the UK. Damnit America, looks like you’re stuck with either Captain Warp Speed or Joe the Kiddy Fondler. As citizen of a country currently led by a vewy angwee* pwime minista who has been known to frequent Thai “Happy Ending” massage parlours to rewieve the stwess of fedwal powitics, I feel your pain. *PM Elmer Fudd is still vewy angwee dat wascawwy Austwalians voted ovawelmingwee against his pawly expwained “Voice” wefewendum. PM Fudd had a wot widing on dat wefewendum, and his land-gwabbing gwobawist masters are vewy upset dat it fayled. Share https://substack.com/home/post/p-145590321
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  • Why the Official AIDS Story is a Complete Crock
    The Great Rebranding, 1980s-Style: HIV Was a Sham, Just Like Sars-Cov-2

    Anthony Colpo

    All you youngsters born after the Glomesh era have surely heard of AIDS, but probably have no idea of just how big a deal it was when it burst onto the scene in the early 1980s.

    It was the biggest show in town. Sure, it wasn't as big a deal as what COVID would later be. It wasn't accompanied by 'vaccine' mandates, lockdowns or heavily-armed goons bashing people for sitting peacefully in the park. Instead of masks, there were condoms and paper toilet seat covers. There was no social distancing, only admonitions to avoid unprotected sex and not share needles when shooting up.

    Fauci was there, front and center, but he wasn't telling us to wear two condoms at once. Instead, he was pimping a toxic concoction known as AZT.

    Right off the bat, nothing made sense about the AIDs charade. It does make sense in hindsight if you view it as a giant test run, an exercise in spreading 'virus' hysteria. The HIV/AIDS charade confirmed most people don't ask questions, and those who do can be quickly shouted over and marginalized as "deniers," "conspiracists" and menaces to society. It also confirmed that not only could people be convinced to take toxic drugs in response to an overblown 'pandemic' scare, but they could be manipulated into rabidly demanding their expedited release.

    It was an exercise whose lessons would prove valuable come December 2019.

    AIDS stands for "acquired immunodeficiency syndrome." In other words, you somehow "acquired" an immune system that, like a tired car engine with 300,000 km on the clock, was about to blow its last gasket.

    It was first identified in 1981 in Los Angeles when the CDC reported on five young homosexual men suffering pneumonia caused by a protozoon known as Pneumocystis carinii.

    This microbe is ordinarily innocuous and, in fact, found in nearly all healthy persons. For reasons unknown it had suddenly become lethal - an outcome previously seen only in persons whose immune systems were being undermined by immunosuppressant therapy, cancer, or severe malnourishment.

    This same pneumonia promptly appeared in New York, together with several dozen cases of an unusual skin cancer called Kaposi's Sarcoma which had previously been almost unknown in the US.

    Eventually Pneumocystis carinii pneumonia and Kaposi's Sarcoma were interpreted as secondary manifestations of an underlying immune-system deficiency of unknown origin which was eventually dubbed "acquired immunodeficiency disease syndrome" or AIDS.

    The bodies of AIDS patients seemed to have just given up. Patients suffered severe weight loss and lethargy and were so immune deficient that even a minor infection threatened to kill them.

    The first few thousand cases were found mostly in homosexual males, and the media bombarded us with images of emaciated gay blokes on the verge of death and barely able to sit upright. Initially, the condition was referred to as GRID (gay-related immune deficiency). Outside of scientific circles, it came to be known as the "gay plague" and religious fundamentalists trumpeted the phenomenon as God's revenge on evil sodomites.

    That began to change in 1983, when AIDS was found to affect heterosexual women, which caused the fear porn to increase by an order of magnitude. As with COVID, health authorities treated us to an orgy of fearmongering and doomsday predictions - and the sheeple lapped it up.

    In 1986, Dr. Donald Ian Macdonald, then Acting Assistant Secretary of Health and Human Services, described "the escalating AIDS epidemic" as "staggering," "devastating" and a "huge problem."

    Dr. Halfdan Mahler, Danish physician and head of the World Health Organization, called AIDS "a health disaster of pandemic proportions" and said he could "not imagine a worse health problem in this century."

    "We stand nakedly in front of a very serious pandemic as mortal as any pandemic there ever has been," Mahler bizarrely quipped. Why he would don his birthday suit instead of a Hazmat one in the face of such a mortal pandemic was never explained, but that's globalist bureaucrats for you.

    "I don't know of any greater killer than AIDS, not to speak of its psychological, social and economic maiming," continued Mahler, who after leaving WHO became director of the International Planned Parenthood Federation.

    Not to be outdone, in 1987 Harvard biology professor Stephen Jay Gould, said AIDS was "potentially, the greatest natural tragedy in human history." He warned "AIDS may run through the entire population, and may carry off a quarter or more of us" (in 1987, the world population was just over 5 billion; it now stands at over 8 billion).

    That same year, Gallup asked an open-ended question about what Americans saw as the most urgent health problem facing the US. Despite the fact AIDS has never even come close to being the leading cause of death in the US, more than two-thirds of Americans said AIDS. The disease continued as the top pick until 2000.

    According to Gallop polls conducted in 1987, most Americans (60%) agreed people with AIDS should be made to carry a card noting they had the disease, and one in three (33%) agreed employers should be allowed to fire employees who had AIDS. Twenty-one percent of Americans said people with AIDS should be isolated from the rest of society.

    An earlier LA Times poll from 1985 found more than half of US adults supported quarantining AIDS patients, nearly half would approve of ID cards for those testing positive for "AIDS antibodies," and one in seven favored tattooing those with the disease.

    People never learn.

    A Disease Looking For a Cause

    Authorities had presented us with a new public health scare, but no causal agent. No-one knew what caused the immune systems of AIDS patients to become so deficient.

    Was it a new microbe? A new drug scourge? God's revenge for Abba and Disco Duck?

    No-one knew.

    At least officially.

    In reality, authorities knew damn well what was going on.

    But they didn’t tell us. Instead, they eventually claimed AIDS was the result of a 'novel virus' that, in 1986, was named "human immunodeficiency virus,” or HIV.

    The 'novel virus' paradigm holds that a 'zoonotic' virus wakes up one day, and decides to "jump" from apes/bats/pangolins/garden gnomes to humans. This novel virus then acts like a seventeen year old that has been given the keys to an alcohol-filled mansion while mom and dad head off for a weekend vacation. However, the virus has no friends to party with. So he first has to convert to a 'human' form of the virus, then he has to begin self-replicating in order to build a social circle. Once this is done, the virions party so hard that the host becomes sick. The virions conclude their current host is no fun, so they go looking for a new host to party inside. The process repeats itself, and before you know it, there's a 'pandemic' going on with squillions of little virions pogo-dancing in global synchrony and chanting "the roof, the roof, the roof is on fire!!" while trashing everything in sight.

    Viruses these days, sheesh.

    Setting aside the glaring fallacies of the virus 'isolation' charade, the 'novel virus = pandemic’ theory is an inherent load of cobblers.

    Outbreaks of what look to be infectious illnesses don't just happen for no reason. There has to be some facilitating factor.

    AIDS became a big thing in the early 1980s, and we know that initially, the majority of patients were gay males. African-Americans were also known to be at increased risk.

    Even if butt sex is an especially efficient method of transmitting STDs, it doesn't explain why AIDS became a phenomenon in the 1980s. After all, both sodomy and homosexuality have been around as long as humans have. Heck, even apes have been observed taking rides on the Hershey Highway.

    Which begs the question: What other events with the potential for dire impact on health occurred around the same time as the AIDS outbreak?

    The Other Crack Rears Its Ugly Head

    Thanks in no small part to Uncle Sam and his ability to conveniently look the other way when it suits his financial and geopolitical interests*, the early 1980s saw a massive flood of cocaine into the US, with urban black neighborhoods the worst afflicted.

    So plentiful was the supply of cocaine, drug dealers came up with a way to make it even cheaper and more addictive in order to expand their customer base.

    Freebase is the name given to the original form of smokable coke, which resulted in a more intense high than snorting. While this constituted an obvious selling point, the process for making freebase required ether, making it notoriously volatile and dangerous to produce. In a famed 1980 incident, comedian Richard Pryor suffered severe and life-threatening burns after mixing cocaine with ether at his home; the mixture promptly exploded in his face.

    Freebase cocaine seems to have first surfaced in the US in the mid-1970s. Around 1980, a less volatile but similar process was developed by dealers in which cocaine was dissolved in a solution of water and baking soda and then dried out into "crack rocks." As the rocks are heated, it makes a crackling sound, hence the name.

    As early as 1981, reports of crack appeared in Los Angeles, San Diego, Houston, and in the Caribbean. Its use quickly spread to other major US cities, and by 1987, crack was reportedly available in DC and all but four states in the Union.

    "In some major cities, such as New York, Detroit, and Philadelphia, one dosage unit of crack could be obtained for as little as $2.50," writes the US DEA. "Never before had any form of cocaine been available at such low prices and at such high purity."

    The crack epidemic dramatically increased the number of Americans addicted to cocaine, as well as the number of cocaine-related hospital emergencies. In 1985, cocaine-related hospital emergencies rose by 12 percent, from 23,500 to 26,300. In 1986, these incidents increased 110 percent, from 26,300 to 55,200.

    The crack cocaine explosion, you'll notice, overlaps neatly with the AIDS "explosion."

    The House of Representatives Select Committee on Narcotics Abuse and Control held cocaine hearings in July, October, and November 1980. Dr. Robert Byck, who along with his colleagues conducted the first scientific studies of cocaine plasma levels after coca paste smoking, testified at the hearings. He warned that the heavy use of smokable freebase cocaine, employed by an estimated 10 percent of cocaine users, was about to change. He warned Congress that the US was about to experience the worst epidemic of drug abuse the country had ever seen. Byck predicted the use of smoked cocaine in the 1980s would match the widespread use of "speed" (methamphetamine) in the 1960s. He urged Congress and the National Institute on Drug Abuse to mount an education and prevention campaign to avert this impending epidemic.

    No such campaign was undertaken.

    "The emergence of crack cocaine use in the United States during the mid-1980s was one of the most significant public health problems of that era," note Watkins et al in a 1998 paper. "Crack use contributed to a series of sexually transmitted disease epidemics, to epidemic increases in violent injuries and homicides, and to significant increases in the incidence and prevalence of cocaine addiction. Despite these threats to health and safety, a national public health campaign to counter crack-related morbidity and mortality was never mounted."

    Is that because authorities were already committed to carrying out a manufactured 'HIV' crisis?

    Crack, Risky Sex, and 'HIV'

    A 1994 NEJM article reported an analysis of 1,967 people recruited from inner-city neighborhoods in New York, Miami, and San Francisco. All respondents reported never having injected drugs, however 1,137 were regular smokers of crack. The remaining 830 people reported never having smoked crack.

    The results for crack users weren't pretty.

    Female crack users were 4.1 times more likely to have been raped, and 1.6 times more likely to have had their first vaginal or anal sex encounter before 13 years of age.

    Both male and female crack users reported a higher number of sexual partners than non-users; in the case of women, crack users were 11 times more likely to have had 50 or more sexual partners.

    Crack-smoking women were 13.5 times more likely than nonsmoking women to have engaged in sexual work at any time, and 28.8 times more likely to have engaged in recent, unprotected sex work.

    Male crack smokers, meanwhile, were 3.4 times more likely to report ever having homosexual anal sex, and 23 times more likely to have had 50 or more male anal sex partners.

    Clearly, crack users were significantly more likely to engage in prostitution and risky sexual practices.

    Not surprising then, that female and male crack users had higher historical rates of syphilis (3.5 and 2.2, respectively) and gonorrhea (1.8 and 1.6, respectively).

    When the researchers ran blood tests for current infection, female and male crack users were significantly more likely to test positive for syphilis (2.8 and 1.6, respectively).

    Among the participants in New York and Miami, HIV 'infection' was 2.3 times more prevalent among crack smokers than among nonsmokers (prevalence of HIV antibodies among participants recruited in San Francisco was low).

    Testing positive for ‘HIV antibodies’ was strongly associated with previous or current infection with other STDs.

    A positive reactive syphilis test (adjusted odds ratio, 2.3) and a history of herpes (adjusted odds ratio, 3.6) remained significantly associated with HIV infection after adjustment for high-risk sexual practices and African-American race.

    Other studies found similar results.

    Chiasson and colleagues at the New York City Department of Health examined the link between HIV infection and crack use. Examining patients at an STD clinic in the South Bronx, they found that, among women with no other identified risk (i.e., no injectible drug use), crack use, prostitution, crack-using prostitution and history of syphilis were all found to be risk factors for HIV infection. Among men with no other risk behavior, a history of syphilis was in fact the strongest predictor of HIV infection - greater than crack use and contact with prostitutes.

    In a 1990 paper, Greenspan and Castro note "between 1981 and 1983, the incidence of primary and secondary syphilis in the United States increased 34%, reaching a rate in 1989 (18.4 cases per 100,000 persons) that was higher than at any time since 1949. Between 1985 and 1989, incidence among blacks more than doubled, from 52.5 to 121.8 cases per 100,000; the increase was greater for black women than for black men (176% versus 106%). These trends are markers for the same high-risk sexual practices that promote transmission of HIV."

    So crack, syphilis and ‘HIV’ are closely related. Now let's look at another class of drugs showing a close correlation with pre-existing STDs and ‘HIV.’

    The Popper Phenomenon

    “Poppers” is a slang term for nitrite inhalant drugs (when they were first manufactured, they came in small ampoules that were 'popped' to release fumes). Amyl nitrite was originally developed to treat angina pectoris by dilating blood vessels, allowing the heart to get more oxygen and thereby relieving the pain.

    Arteries are not the only thing poppers help to dilate. Inhaling nitrites relaxes smooth muscles throughout the body - including the sphincter muscles, making it particularly helpful to gay posteriors. Along with facilitating anal sex, the blood vessel-dilating effects of poppers can produce a brief but intense sensation of heat and euphoria lasting 1 or 2 minutes.

    The story of poppers is an interesting one, involving US Vietnam vets, a profiteering Big Pharma and an enabling FDA, a gay medical student and organized criminals.

    The latter two entities sidestepped an eventual prescription requirement for amyl nitrite by creating butyl and isobutyl nitrite - less pure, more toxic, and even faster-acting versions than the original. Further restrictions were averted thanks to an unwritten agreement between producers and the FDA that poppers were only to be advertised in gay-oriented publications, as 'room deodorizers.'

    During the 1970s and early 80s, poppers were advertised heavily in the gay press, and the drugs became an integral part of gay culture. Not only was it routine for patrons at gay nightclubs to freely pass the vials around, some "disco clubs would even add to the general euphoria by occasionally spraying the dance floor with poppers fumes."

    "The miasma of nitrite fumes was taken for granted at gay gathering places: bars, baths, leather clubs," writes John Lauritsen in a 1994 New York Native article. "Some gay men were never without their little bottle, from which they snorted fumes around the clock."

    Throwing caution to the wind when it comes to drugs never ends well. Amyl nitrite was developed for occasional use by angina patients, not as a party drug to be snorted every time one hit the dance floor or engaged in a bout of Jolly Rogering.

    Apart from causing localized damage to nasal membranes, poppers have been linked to anemia, strokes, heart, lung, and brain damage, cardiovascular collapse, and, tellingly, the blood de-oxygenation, thymus atrophy, chronic depletion of T-cell ratio's associated with severe immune dysfunction. The drugs have also been linked to the development of Kaposi's Sarcoma.

    Sounds a lot like AIDS, doesn't it?

    While researchers and the more level-headed of gay advocates warned of the dangers, the FDA continued to look the other way. The gay press, whose advertising revenue relied heavily on popper ads, also willfully turned a blind eye to the dangers.

    In the 1980s, in a lukewarm attempt to be seen to be doing something about the problem, US health officials banned the use of poppers in public places and required merchants to post warnings about their dangers. "The warnings about their use disappeared sometime in the late '80s to early '90s," reports SFGATE, "and no one seems to know why."

    "During the first few years of the AIDS epidemic," writes Ian Young at VirusMyth.org, "poppers came under suspicion as a possible contributing factor. But after 1984, when the Reagan administration pronounced a single retrovirus to be the only cause of the growing list of AIDS illnesses, the health hazards of poppers were dismissed. All attention and funding was directed to HIV."

    Fun fact: Burroughs Wellcome, the original manufacturers of poppers, went on to profit handsomely from the subsequent AIDS hysteria with its highly-toxic 'anti-AIDS' drug AZT.

    History is Made (Up)

    There were major drug scourges afflicting the high-risk gay and African-American communities, drugs whose chronologies overlapped neatly with the AIDS outbreak. Use and abuse of these drugs was well established to cause severe illness, immune dysfunction and was also strongly correlated with pre-existing STDs like syphilis.

    The powers-that-be, however, had already decided the sole cause of AIDs was a 'novel virus.' They just needed to come up with one.

    And so along came the virologists to save the day. Not just any old bunch of virologists, but virologists with friends in high places. In France, this meant Luc Montagnier and his team at the Pasteur Institute, which advises the French government and the World Health Organization (WHO), and maintains a close collaboration with the US Centers for Disease Control and Prevention (CDC).

    In the US, it meant sci-bureaucrats from the government's behemoth National Institutes of Health (NIH). One of the key figures was the caustic Robert S Gallo, a researcher at the NIH's National Cancer Institute, where he worked for 30 years mainly as head of the Laboratory of Tumor Cell Biology. Gallo’s career would be dogged by controversy and misconduct allegations, but that’s a whole other article (stay tuned).

    The other career bureaucrat that would play a key role on the US side was none other than Anthony S Fauci, who recently completed a ridiculous 38-year reign as unelected head of the NIH's National Institute of Allergy and Infectious Diseases (NIAID).

    If you've surmised that, with names like the above, the HIV story must be a real shite show, you are absolutely correct.

    HIV is Invented 'Discovered'

    In 1983, the Pasteur Institute researchers declared they had 'isolated' a 'retrovirus' belonging to the family of T-cell leukemia viruses (HTLV), and concluded it "may be involved in several pathological syndromes, including AIDS." (Bold emphasis added)

    Their isolate came from a promiscuous 33-year-old Caucasian homosexual male referred to as "BRU", who indicated he'd had more than 50 sexual partners per year. Nasty. According to the authors, he displayed "signs and symptoms that often precede the acquired immune deficiency syndrome (AIDS)." However, the only symptoms reported for the patient were multiple lymphadenopathies (swollen lymph glands) and asthenia (weakness), which are evident in many conditions aside from AIDS. Neither fever nor recent loss of weight were noted.

    In other words, the patient from whom the alleged AIDS-causing virus was first 'isolated' from did not have an AIDS diagnosis.

    Tellingly, the patient did have a history of several episodes of gonorrhea and had been treated for syphilis in September 1982. Lymphadenopathy is one of the symptoms of both the aforementioned infections.

    The study's lead author was Francoise Barre-Sinoussi, although the finding is routinely credited to the paper's last listed author, the late Montagnier.

    The French study was marred by two key problems. It did not isolate any virus, and it did not show AIDS was caused by any HTLV offshoot.

    Forty years later, little has changed. The terminology and rationalizations have indeed become increasingly complex (as is the case with most elaborate lies), but there is no physical isolate of 'HIV.'

    Virologists and their sycophants, of course, insist this doesn't matter and that their non-purified mixtures are indeed isolates.

    While they condescendingly sneer and dismiss anyone who disputes this as a silly little dumb-dumb that doesn't 'understand' virology, they tend to remain rather quiet on another highly inconvenient observation.

    Namely, there is no proof that whatever is in their ‘isolates’ actually causes AIDS.

    HIV and Sars-Cov-2: The 'Deadly' Viruses That Aren't Deadly

    In the early days of 'COVID', testing positive for the mythical Sars-Cov-2 was considered a death sentence. So much so, that some folks didn't even bother getting their affairs in order; they instead killed themselves.

    Such is the power of all this heinous "deadly virus" bullshit.

    It was the same in the 'HIV' Dark Ages - testing positive was considered a death sentence. When a famous basketballer by the name of Erving “Magic” Johnson announced he was HIV positive in 1991, everyone was shocked. "Now we all know someone with HIV," said someone I can't recall in what was supposed to be a profound, insight-triggering moment.

    Johnson, everyone assumed, was now living on borrowed time.

    Thirty-three years later, Johnson is still alive and wealthy. He attributes his survival to antiretroviral cocktails that have never been shown in clinical studies to benefit survival: GlaxoSmithKline's Trizivir and Abbott's Kaletra. These cocktails are comprised of drugs like AZT which increase the risk of side effects but have never been shown to exert a mortality benefit.

    Johnson, it should be noted, has featured in ads for both products. In 2009, the FDA issued a warning letter to Abbott Laboratories regarding a promotional DVD in which Johnson discussed his experiences with Kaletra. The letter stated the violations were of public health concern "because they suggest that Kaletra is safer and more effective than has been demonstrated by substantial evidence or substantial clinical experience, and encourage use in circumstances other than those for which the drug has been shown to be safe and effective."

    "FDA is not aware of substantial evidence or substantial clinical experience to support effectiveness for five or more years of treatment with Kaletra in treatment-experienced adults. The personal experience of Kaletra patients, such as Magic Johnson, does not constitute such evidence."

    So if overpriced drug cocktails aren't keeping Johnson alive, what explains his survival?

    It's explained by the fact that HIV is a load of bollocks. A shady test that claims you are ‘HIV positive’ does not mean you are in fact harboring a deadly 'virus.'

    If ‘HIV’ was so deadly, then lab animals infected with it would get sick and die.

    But guess what? Administering a so-called isolate of uber-deadly HIV to animals results in ... nothing.

    Stugatz.

    That's right - directly administering the Virus That Causes AIDS™ to animals does not cause AIDS.

    "The only animals susceptible to experimental HIV-1** infection are the chimpanzee, gibbon ape, and rabbit but AIDS-like disease has not yet been reported in these species," lamented the authors of a 1989 FASEB paper.

    Oops.

    I'm guessing those chimps, gibbons and wascawwy wabbits didn't have a history of syphilis, smoking crack or inhaling poppers.

    Experiments in which human volunteers are deliberately 'infected' with the 'HIV isolate' would never get past the ethics committees of most research institutions.

    We do, however, have numerous instances of involuntary infection to give us a guide as to what happens when otherwise low-risk individuals are exposed to 'HIV.'

    In a 1984 NEJM letter, before 'HIV' testing became available, Sloan Kettering researchers reported there had been 27 parenteral exposures by 25 staff to the blood of AIDS patients since August 1982 (24 exposures were via needlestick).

    "All the involved staff are in their usual (generally excellent) state of health," including those who were exposed more than 12 months ago. Blood work was available for 12 staff with exposure more than 6 months prior, and no abnormalities were evident, reported the researchers.

    During 1985–2013, 58 confirmed and 150 possible cases of occupationally acquired HIV infection among healthcare workers were reported to the CDC. Since 1999, only one confirmed case (a laboratory technician sustaining a needle puncture while working with a live HIV culture in 2008) has been reported. There is no mention of subsequent AIDS, something the fear-porn agents at the CDC would surely have mentioned had it occurred.

    Some of you have probably heard of Dr Robert Willner, who twice deliberately pricked himself on TV with blood from 'HIV-positive' men (in Spain 1993, and USA 1994). Willner was an outspoken critic of the HIV hypothesis, having authored a book titled Deadly Deception: The Proof that Sex and HIV Absolutely Do Not Cause AIDS. Depending on who you listen to, Willner died 3 months after his 1994 TV appearance in a car crash, or the following year from a heart attack. Neither outcome is consistent with the oft-cited sequelae of AIDS.

    Jump, Jump, Jump Around

    Despite the fact that it is scientifically untenable, the HIV theory of AIDS still reigns supreme. Which brings us back to the key question: Why did 'HIV' wait until Wham! and Devine hit the charts before it started striking down gay blokes en mass?

    Enter the apes.

    According to Wikipedia, "HIV made the jump from other primates to humans in west-central Africa in the early-to-mid-20th century." (Bold emphasis added)

    Just like Sars-Cov-2 was purported to have kicked off when the allegedly zoonotic virus "jumped" to humans from a bat or pangolin at a Wuhan wet market that did not sell any bats or pangolins.

    Says Wikipedia, "Scientists generally accept that the known strains (or groups) of HIV-1 are most closely related to the simian immunodeficiency viruses (SIVs) endemic in wild ape populations of West Central African forests." (Bold emphasis added).

    "Generally accept" is code for "Scientists have no proof of this, but pretend it's true anyway."

    This brings us to an oft-cited 2011 paper titled "Origins of HIV and the AIDS Pandemic" which repeats the claim that "simian immunodeficiency viruses (SIVs) ... crossed from monkeys to apes and from apes to humans." The paper was authored by Paul Sharp and Beatrice Hahn, the latter a member of Gallo's NCI lab team which she joined in 1982.


    A chimpanzee minding his own business while a Gallo associate who blames apes for spreading HIV to humans (Beatrice Hahn) stares at him from a distance.
    In their paper, the researchers provide a graphic claiming SIV resulting in HIV-1 has been transmitted to humans via chimpanzees and gorillas.

    Hold that thought.

    According to the official narrative, the primary routes of 'HIV' transmission in humans are sexual intercourse with an infected individual, sharing needles with an infected person while taking drugs, transfusions of infected blood, or transmission from an infected pregnant mother to fetus.

    Sharp and Hahn speculate that SIVs first developed in chimpanzees, and were spread among the chimpanzee community primarily through sexual activity, from infected mothers to infants, and "in rare cases, possibly by aggression."

    But how did the disease "jump" from apes to humans? Researchers can't claim humans and apes were shooting up drugs together and sharing needles while doing so, or that apes were administering blood transfusions to humans, because that would be patently absurd.

    Ditto for suggesting apes were passing SIV to humans via birth, because apes don't give birth to humans.

    Claiming that apes transmitted SIV to humans because they were having cross-species sexual encounters would also be a hard sell. Humans are capable of some pretty weird and degenerate behaviour, but good luck pinning down a chimp or gorilla while you attempt to get jiggy with it.


    Meet Bruce. Can bench press you and your extended family with one arm. Incursions into his personal space not advised.
    "How humans acquired the ape precursors of HIV-1 groups M, N, O, and P is not known," write Sharp and Hahn, "however, based on the biology of these viruses, transmission must have occurred through cutaneous or mucous membrane exposure to infected ape blood and/or body fluids. Such exposures occur most commonly in the context of bushmeat hunting." (Bold emphasis added).

    Researchers can't explain exactly how immunodeficiency viruses pole-vaulted from apes to human, so they simply assume it must have happened during hunting expeditions.

    Virologists do a lot of assuming.

    Sharp and Hahn write that the first clue to HIV-1's "sudden emergence, epidemic spread, and unique pathogenicity" came in 1986 when a “morphologically similar but anti-genically distinct” virus was allegedly found to cause AIDS in patients in western Africa.

    Well riddle me this, Batman: Humans have been around for 2.5 million years, and the earliest Homo sapiens were getting around some 300,000 years ago.

    We've been hunting that whole time.

    Furthermore, the advance of agriculture and the steadily declining numbers of hunter-gatherers in modern times would have meant a greatly reduced opportunity for SIV to jump aboard the H-train via scratchy-bitey-fluid-exchangey hunting confrontations.

    Yet immunodeficiency viruses waited until the latter half of the Twentieth Century to successfully make the big cross-species jump?

    What an utter crock.

    Wikipedia admits "How the SIV virus would have transformed into HIV after infection of the hunter or bushmeat handler from the ape/monkey is still a matter of debate."

    Translated: There is no actual scientific evidence to support the claim that, after allegedly entering the human body, ‘SIV’ magically transformed into ‘HIV.’

    The Sodomy Paradox

    There's another problem with the official AIDS narrative which holds that, after catching SIV from apes during hunting mishaps in Africa, it "transformed" into HIV, which hunter-gatherers then spread by doing the backdoor boogie with gay abandon.

    That story further holds that, somewhere along the way, one of these HIV-carrying ape-hunters nailed a gay airline steward from America. Patient Zero then flew back to the US, and began having lots of AIDS-causing unprotected sex in the saunas of San Francisco. Or the gay bars of New York. Or the wet markets of Wisconsin, I'm not sure, all this virus BS gets a bit hard to keep track of after a while.

    It doesn't really matter, because like the rest of the AIDS tale, the gay airline steward story was nonsense. Gaetan Dugas, the French-Canadian flight attendant posthumously labelled 'Patient Zero' and accused of single-handedly igniting the spread of HIV/AIDS across North America, was later exonerated.

    Thanks to the determined sleuthing of Pullitzer Prize-winning reporter John Crewdson, it was known by 1988 that what we now call AIDS was in fact present in America in the 1960s. While the rest of the media was tripping over itself to blame Dugas (“THE MAN WHO GAVE US AIDS” blared the New York Post’s October 6, 1987 headline; “Canadian Said to Have Had Key Role in Spread of AIDS,” wrote the New York Times, while the National Review nicknamed Dugas “the Columbus of AIDS"), Crewdson had discovered a 1973 case report that showed the official Patient Zero story was bollocks.

    That 1973 case report described Robert Rayford, a 15-year-old black lad from St. Louis who had died of AIDS in 1969 - more than a decade before anyone knew what AIDS was. The impoverished teen had presented to hospital in the spring of 1968 with swollen loins covered with open, infected sores. He struggled while breathing, was razor thin and pale as a ghost. Doctors initially suspected cancer, but subsequent tests revealed herpes, genital warts, and a severe case of chlamydia. The infection spread, in the form of purple colored lesions, to his legs, causing a misdiagnosis of lymphedema. He eventually succumbed to his condition in May 1969, leaving doctors baffled.

    The teen, who doctors described as mildly intellectually impaired, said he'd suffered the symptoms for around two years prior to seeking medical help. He denied injury or animal bites, had not travelled outside the midwestern United States, but admitted to "frequent" heterosexual intercourse. His family consented to an autopsy, which revealed "widespread Kaposi's sarcoma of the aggressive, disseminated type." The autopsy also found evidence of anal scarring and a particular kind of lesion no one had identified when Rayford was alive. Some doctors thought the scarring indicated Rayford was gay; others pointed out he may have been sexually abused.

    Struck by how closely Rayford's symptoms resembled those of AIDS, Crewdson flew to St. Louis and found a pathologist willing to dig through laboratory freezers in search of the youth's tissue samples. By using the test 'co-developed' by Gallo and the French, researchers were able to determine that the boy, incredibly, had been infected with 'HIV.'

    The finding was published in JAMA in 1988. However, it was not until 2016 that the fake Dugas tale was officially revoked.

    Had the Rayford story been more widely known, it wouldn’t have been good for HIV business.

    Not to worry, the out-of-Africa hypothesis was salvaged in 1998 when researchers claimed they had detected HIV - by a PCR process involving two rounds of amplification for a combined total of 69 cycles - in a plasma sample obtained in early 1959 from an adult Bantu male, with a sickle-cell trait and a glucose-6-phosphate-dehydrogenase deficiency, living in the Belgian Congo. Two of the researchers announcing this narrative-saving discovery hailed from the Aaron Diamond AIDS Research Center, at Rockefeller University in New York.

    So just like the COVID charade, we have a shamdemic for which the original Patient Zero story was shown to be a bunch of cobblers. Just like the COVID sham, few people noticed or cared and the rest of the AIDS tale continued its relentless march and took on a life of its own.

    Despite more holes than a ... wait, that's dangerous pun territory ... I mean, despite a plethora of discrepancies, the official Fauci-endorsed tale still has HIV migrating from Africa to the US and spread in the early 1980s by blokes bumping uglies in big city gay bars and saunas.

    And Fauci should know, because he went to gay saunas and gay bars himself in the “early stages” of the AIDS “explosion” to get a “feel” for the situation.

    Purely for ‘research’ purposes, of course (wink, wink).

    It's okay Tony, it's 2024, you don't have to cover for your sexuality anymore.


    A young Anthony Fauci displaying his "I've just been to the saunas!" smile. Your tax money at work.
    You could literally fill a book with all the discrepancies contained within the official AIDS story; several authors have already done just that. What I wanted to highlight here are the commonalities between the AIDS and COVID sagas.

    Both featured never-isolated 'viruses' with nonsensical 'Patient Zero' stories.

    ‘Isolates’ of both these ‘deadly’ and ‘novel’ viruses do a whole lot of nothing when administered to our primate cousins.

    Both sagas featured Anthony Fauci, showing up on cue touting the most toxic drug he could get away with recommending.

    Both featured doomsday, end-of-times hyperbole in which testing 'positive' was initially considered a death sentence.

    Both were remarkable demonstrations of how the media and masses could be easily manipulated into accepting a pandemic scare that, upon the most cursory examination, simply didn't add up.


    *During the presidency of former actor Ronald Reagan, senior administration officials secretly — and illegally — arranged for the sale of arms to Iran in return for Iran’s promise to help secure the release of a group of Americans being held hostage in Lebanon.

    Suspiciously, the hostages were formally released into US custody just minutes after Reagan was sworn into office.

    Proceeds from the arms sales were then secretly, and again illegally, funneled to the Contras, a group of rebels fighting the Marxist Sandinista government of Nicaragua.

    Is if that wasn't bad enough, the CIA looked the other way while the Contras trafficked cocaine into the US to help finance their fight to oust the communist Sandinistas. The scandal was exposed in 1996 by the brilliant, Pullitzer Prize-winning journalist Gary Webb while writing for the San Jose Mercury News. His series described a San Francisco Bay Area drug ring that sold tons of cocaine to the Crips and Bloods street gangs of Los Angeles, funelling millions in drug profits to the CIA-assisted Contras. This drug ring "opened the first pipeline between Colombia's cocaine cartels and the black neighborhoods of Los Angeles" and, as a result, "helped spark a crack explosion in urban America."

    His articles caused a proverbial shit-storm, prompting the government to conduct several investigations into itself and declaring itself innocent of all charges. We were supposed to believe it was all just an accidental oversight when even the Kerry report acknowledged "the Contra drug links included", among other connections, "... payments to drug traffickers by the U.S. State Department of funds authorized by the Congress for humanitarian assistance to the Contras, in some cases after the traffickers had been indicted by federal law enforcement agencies on drug charges, in others while traffickers were under active investigation by these same agencies." (Bold emphasis added).

    The Los Angeles Times, New York Times, and Washington Post launched their own 'investigations' (read: hatchet jobs) and rejected Webb's allegations, instead siding with the government - a practice they uphold to this day.

    However, an internal CIA report released in 1998 admitted the CIA ‘overlooked’ or ‘ignored’ reports that the Nicaragua Contra rebels financed their fight to oust the communist Sandinistas through the sale of drugs in the United States.

    **‘HIV-1’ is the form of ‘HIV’ allegedly most common and threatening to humans. According to the official tale, ‘HIV-2’ is rare and of little threat.

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    Why the Official AIDS Story is a Complete Crock The Great Rebranding, 1980s-Style: HIV Was a Sham, Just Like Sars-Cov-2 Anthony Colpo All you youngsters born after the Glomesh era have surely heard of AIDS, but probably have no idea of just how big a deal it was when it burst onto the scene in the early 1980s. It was the biggest show in town. Sure, it wasn't as big a deal as what COVID would later be. It wasn't accompanied by 'vaccine' mandates, lockdowns or heavily-armed goons bashing people for sitting peacefully in the park. Instead of masks, there were condoms and paper toilet seat covers. There was no social distancing, only admonitions to avoid unprotected sex and not share needles when shooting up. Fauci was there, front and center, but he wasn't telling us to wear two condoms at once. Instead, he was pimping a toxic concoction known as AZT. Right off the bat, nothing made sense about the AIDs charade. It does make sense in hindsight if you view it as a giant test run, an exercise in spreading 'virus' hysteria. The HIV/AIDS charade confirmed most people don't ask questions, and those who do can be quickly shouted over and marginalized as "deniers," "conspiracists" and menaces to society. It also confirmed that not only could people be convinced to take toxic drugs in response to an overblown 'pandemic' scare, but they could be manipulated into rabidly demanding their expedited release. It was an exercise whose lessons would prove valuable come December 2019. AIDS stands for "acquired immunodeficiency syndrome." In other words, you somehow "acquired" an immune system that, like a tired car engine with 300,000 km on the clock, was about to blow its last gasket. It was first identified in 1981 in Los Angeles when the CDC reported on five young homosexual men suffering pneumonia caused by a protozoon known as Pneumocystis carinii. This microbe is ordinarily innocuous and, in fact, found in nearly all healthy persons. For reasons unknown it had suddenly become lethal - an outcome previously seen only in persons whose immune systems were being undermined by immunosuppressant therapy, cancer, or severe malnourishment. This same pneumonia promptly appeared in New York, together with several dozen cases of an unusual skin cancer called Kaposi's Sarcoma which had previously been almost unknown in the US. Eventually Pneumocystis carinii pneumonia and Kaposi's Sarcoma were interpreted as secondary manifestations of an underlying immune-system deficiency of unknown origin which was eventually dubbed "acquired immunodeficiency disease syndrome" or AIDS. The bodies of AIDS patients seemed to have just given up. Patients suffered severe weight loss and lethargy and were so immune deficient that even a minor infection threatened to kill them. The first few thousand cases were found mostly in homosexual males, and the media bombarded us with images of emaciated gay blokes on the verge of death and barely able to sit upright. Initially, the condition was referred to as GRID (gay-related immune deficiency). Outside of scientific circles, it came to be known as the "gay plague" and religious fundamentalists trumpeted the phenomenon as God's revenge on evil sodomites. That began to change in 1983, when AIDS was found to affect heterosexual women, which caused the fear porn to increase by an order of magnitude. As with COVID, health authorities treated us to an orgy of fearmongering and doomsday predictions - and the sheeple lapped it up. In 1986, Dr. Donald Ian Macdonald, then Acting Assistant Secretary of Health and Human Services, described "the escalating AIDS epidemic" as "staggering," "devastating" and a "huge problem." Dr. Halfdan Mahler, Danish physician and head of the World Health Organization, called AIDS "a health disaster of pandemic proportions" and said he could "not imagine a worse health problem in this century." "We stand nakedly in front of a very serious pandemic as mortal as any pandemic there ever has been," Mahler bizarrely quipped. Why he would don his birthday suit instead of a Hazmat one in the face of such a mortal pandemic was never explained, but that's globalist bureaucrats for you. "I don't know of any greater killer than AIDS, not to speak of its psychological, social and economic maiming," continued Mahler, who after leaving WHO became director of the International Planned Parenthood Federation. Not to be outdone, in 1987 Harvard biology professor Stephen Jay Gould, said AIDS was "potentially, the greatest natural tragedy in human history." He warned "AIDS may run through the entire population, and may carry off a quarter or more of us" (in 1987, the world population was just over 5 billion; it now stands at over 8 billion). That same year, Gallup asked an open-ended question about what Americans saw as the most urgent health problem facing the US. Despite the fact AIDS has never even come close to being the leading cause of death in the US, more than two-thirds of Americans said AIDS. The disease continued as the top pick until 2000. According to Gallop polls conducted in 1987, most Americans (60%) agreed people with AIDS should be made to carry a card noting they had the disease, and one in three (33%) agreed employers should be allowed to fire employees who had AIDS. Twenty-one percent of Americans said people with AIDS should be isolated from the rest of society. An earlier LA Times poll from 1985 found more than half of US adults supported quarantining AIDS patients, nearly half would approve of ID cards for those testing positive for "AIDS antibodies," and one in seven favored tattooing those with the disease. People never learn. A Disease Looking For a Cause Authorities had presented us with a new public health scare, but no causal agent. No-one knew what caused the immune systems of AIDS patients to become so deficient. Was it a new microbe? A new drug scourge? God's revenge for Abba and Disco Duck? No-one knew. At least officially. In reality, authorities knew damn well what was going on. But they didn’t tell us. Instead, they eventually claimed AIDS was the result of a 'novel virus' that, in 1986, was named "human immunodeficiency virus,” or HIV. The 'novel virus' paradigm holds that a 'zoonotic' virus wakes up one day, and decides to "jump" from apes/bats/pangolins/garden gnomes to humans. This novel virus then acts like a seventeen year old that has been given the keys to an alcohol-filled mansion while mom and dad head off for a weekend vacation. However, the virus has no friends to party with. So he first has to convert to a 'human' form of the virus, then he has to begin self-replicating in order to build a social circle. Once this is done, the virions party so hard that the host becomes sick. The virions conclude their current host is no fun, so they go looking for a new host to party inside. The process repeats itself, and before you know it, there's a 'pandemic' going on with squillions of little virions pogo-dancing in global synchrony and chanting "the roof, the roof, the roof is on fire!!" while trashing everything in sight. Viruses these days, sheesh. Setting aside the glaring fallacies of the virus 'isolation' charade, the 'novel virus = pandemic’ theory is an inherent load of cobblers. Outbreaks of what look to be infectious illnesses don't just happen for no reason. There has to be some facilitating factor. AIDS became a big thing in the early 1980s, and we know that initially, the majority of patients were gay males. African-Americans were also known to be at increased risk. Even if butt sex is an especially efficient method of transmitting STDs, it doesn't explain why AIDS became a phenomenon in the 1980s. After all, both sodomy and homosexuality have been around as long as humans have. Heck, even apes have been observed taking rides on the Hershey Highway. Which begs the question: What other events with the potential for dire impact on health occurred around the same time as the AIDS outbreak? The Other Crack Rears Its Ugly Head Thanks in no small part to Uncle Sam and his ability to conveniently look the other way when it suits his financial and geopolitical interests*, the early 1980s saw a massive flood of cocaine into the US, with urban black neighborhoods the worst afflicted. So plentiful was the supply of cocaine, drug dealers came up with a way to make it even cheaper and more addictive in order to expand their customer base. Freebase is the name given to the original form of smokable coke, which resulted in a more intense high than snorting. While this constituted an obvious selling point, the process for making freebase required ether, making it notoriously volatile and dangerous to produce. In a famed 1980 incident, comedian Richard Pryor suffered severe and life-threatening burns after mixing cocaine with ether at his home; the mixture promptly exploded in his face. Freebase cocaine seems to have first surfaced in the US in the mid-1970s. Around 1980, a less volatile but similar process was developed by dealers in which cocaine was dissolved in a solution of water and baking soda and then dried out into "crack rocks." As the rocks are heated, it makes a crackling sound, hence the name. As early as 1981, reports of crack appeared in Los Angeles, San Diego, Houston, and in the Caribbean. Its use quickly spread to other major US cities, and by 1987, crack was reportedly available in DC and all but four states in the Union. "In some major cities, such as New York, Detroit, and Philadelphia, one dosage unit of crack could be obtained for as little as $2.50," writes the US DEA. "Never before had any form of cocaine been available at such low prices and at such high purity." The crack epidemic dramatically increased the number of Americans addicted to cocaine, as well as the number of cocaine-related hospital emergencies. In 1985, cocaine-related hospital emergencies rose by 12 percent, from 23,500 to 26,300. In 1986, these incidents increased 110 percent, from 26,300 to 55,200. The crack cocaine explosion, you'll notice, overlaps neatly with the AIDS "explosion." The House of Representatives Select Committee on Narcotics Abuse and Control held cocaine hearings in July, October, and November 1980. Dr. Robert Byck, who along with his colleagues conducted the first scientific studies of cocaine plasma levels after coca paste smoking, testified at the hearings. He warned that the heavy use of smokable freebase cocaine, employed by an estimated 10 percent of cocaine users, was about to change. He warned Congress that the US was about to experience the worst epidemic of drug abuse the country had ever seen. Byck predicted the use of smoked cocaine in the 1980s would match the widespread use of "speed" (methamphetamine) in the 1960s. He urged Congress and the National Institute on Drug Abuse to mount an education and prevention campaign to avert this impending epidemic. No such campaign was undertaken. "The emergence of crack cocaine use in the United States during the mid-1980s was one of the most significant public health problems of that era," note Watkins et al in a 1998 paper. "Crack use contributed to a series of sexually transmitted disease epidemics, to epidemic increases in violent injuries and homicides, and to significant increases in the incidence and prevalence of cocaine addiction. Despite these threats to health and safety, a national public health campaign to counter crack-related morbidity and mortality was never mounted." Is that because authorities were already committed to carrying out a manufactured 'HIV' crisis? Crack, Risky Sex, and 'HIV' A 1994 NEJM article reported an analysis of 1,967 people recruited from inner-city neighborhoods in New York, Miami, and San Francisco. All respondents reported never having injected drugs, however 1,137 were regular smokers of crack. The remaining 830 people reported never having smoked crack. The results for crack users weren't pretty. Female crack users were 4.1 times more likely to have been raped, and 1.6 times more likely to have had their first vaginal or anal sex encounter before 13 years of age. Both male and female crack users reported a higher number of sexual partners than non-users; in the case of women, crack users were 11 times more likely to have had 50 or more sexual partners. Crack-smoking women were 13.5 times more likely than nonsmoking women to have engaged in sexual work at any time, and 28.8 times more likely to have engaged in recent, unprotected sex work. Male crack smokers, meanwhile, were 3.4 times more likely to report ever having homosexual anal sex, and 23 times more likely to have had 50 or more male anal sex partners. Clearly, crack users were significantly more likely to engage in prostitution and risky sexual practices. Not surprising then, that female and male crack users had higher historical rates of syphilis (3.5 and 2.2, respectively) and gonorrhea (1.8 and 1.6, respectively). When the researchers ran blood tests for current infection, female and male crack users were significantly more likely to test positive for syphilis (2.8 and 1.6, respectively). Among the participants in New York and Miami, HIV 'infection' was 2.3 times more prevalent among crack smokers than among nonsmokers (prevalence of HIV antibodies among participants recruited in San Francisco was low). Testing positive for ‘HIV antibodies’ was strongly associated with previous or current infection with other STDs. A positive reactive syphilis test (adjusted odds ratio, 2.3) and a history of herpes (adjusted odds ratio, 3.6) remained significantly associated with HIV infection after adjustment for high-risk sexual practices and African-American race. Other studies found similar results. Chiasson and colleagues at the New York City Department of Health examined the link between HIV infection and crack use. Examining patients at an STD clinic in the South Bronx, they found that, among women with no other identified risk (i.e., no injectible drug use), crack use, prostitution, crack-using prostitution and history of syphilis were all found to be risk factors for HIV infection. Among men with no other risk behavior, a history of syphilis was in fact the strongest predictor of HIV infection - greater than crack use and contact with prostitutes. In a 1990 paper, Greenspan and Castro note "between 1981 and 1983, the incidence of primary and secondary syphilis in the United States increased 34%, reaching a rate in 1989 (18.4 cases per 100,000 persons) that was higher than at any time since 1949. Between 1985 and 1989, incidence among blacks more than doubled, from 52.5 to 121.8 cases per 100,000; the increase was greater for black women than for black men (176% versus 106%). These trends are markers for the same high-risk sexual practices that promote transmission of HIV." So crack, syphilis and ‘HIV’ are closely related. Now let's look at another class of drugs showing a close correlation with pre-existing STDs and ‘HIV.’ The Popper Phenomenon “Poppers” is a slang term for nitrite inhalant drugs (when they were first manufactured, they came in small ampoules that were 'popped' to release fumes). Amyl nitrite was originally developed to treat angina pectoris by dilating blood vessels, allowing the heart to get more oxygen and thereby relieving the pain. Arteries are not the only thing poppers help to dilate. Inhaling nitrites relaxes smooth muscles throughout the body - including the sphincter muscles, making it particularly helpful to gay posteriors. Along with facilitating anal sex, the blood vessel-dilating effects of poppers can produce a brief but intense sensation of heat and euphoria lasting 1 or 2 minutes. The story of poppers is an interesting one, involving US Vietnam vets, a profiteering Big Pharma and an enabling FDA, a gay medical student and organized criminals. The latter two entities sidestepped an eventual prescription requirement for amyl nitrite by creating butyl and isobutyl nitrite - less pure, more toxic, and even faster-acting versions than the original. Further restrictions were averted thanks to an unwritten agreement between producers and the FDA that poppers were only to be advertised in gay-oriented publications, as 'room deodorizers.' During the 1970s and early 80s, poppers were advertised heavily in the gay press, and the drugs became an integral part of gay culture. Not only was it routine for patrons at gay nightclubs to freely pass the vials around, some "disco clubs would even add to the general euphoria by occasionally spraying the dance floor with poppers fumes." "The miasma of nitrite fumes was taken for granted at gay gathering places: bars, baths, leather clubs," writes John Lauritsen in a 1994 New York Native article. "Some gay men were never without their little bottle, from which they snorted fumes around the clock." Throwing caution to the wind when it comes to drugs never ends well. Amyl nitrite was developed for occasional use by angina patients, not as a party drug to be snorted every time one hit the dance floor or engaged in a bout of Jolly Rogering. Apart from causing localized damage to nasal membranes, poppers have been linked to anemia, strokes, heart, lung, and brain damage, cardiovascular collapse, and, tellingly, the blood de-oxygenation, thymus atrophy, chronic depletion of T-cell ratio's associated with severe immune dysfunction. The drugs have also been linked to the development of Kaposi's Sarcoma. Sounds a lot like AIDS, doesn't it? While researchers and the more level-headed of gay advocates warned of the dangers, the FDA continued to look the other way. The gay press, whose advertising revenue relied heavily on popper ads, also willfully turned a blind eye to the dangers. In the 1980s, in a lukewarm attempt to be seen to be doing something about the problem, US health officials banned the use of poppers in public places and required merchants to post warnings about their dangers. "The warnings about their use disappeared sometime in the late '80s to early '90s," reports SFGATE, "and no one seems to know why." "During the first few years of the AIDS epidemic," writes Ian Young at VirusMyth.org, "poppers came under suspicion as a possible contributing factor. But after 1984, when the Reagan administration pronounced a single retrovirus to be the only cause of the growing list of AIDS illnesses, the health hazards of poppers were dismissed. All attention and funding was directed to HIV." Fun fact: Burroughs Wellcome, the original manufacturers of poppers, went on to profit handsomely from the subsequent AIDS hysteria with its highly-toxic 'anti-AIDS' drug AZT. History is Made (Up) There were major drug scourges afflicting the high-risk gay and African-American communities, drugs whose chronologies overlapped neatly with the AIDS outbreak. Use and abuse of these drugs was well established to cause severe illness, immune dysfunction and was also strongly correlated with pre-existing STDs like syphilis. The powers-that-be, however, had already decided the sole cause of AIDs was a 'novel virus.' They just needed to come up with one. And so along came the virologists to save the day. Not just any old bunch of virologists, but virologists with friends in high places. In France, this meant Luc Montagnier and his team at the Pasteur Institute, which advises the French government and the World Health Organization (WHO), and maintains a close collaboration with the US Centers for Disease Control and Prevention (CDC). In the US, it meant sci-bureaucrats from the government's behemoth National Institutes of Health (NIH). One of the key figures was the caustic Robert S Gallo, a researcher at the NIH's National Cancer Institute, where he worked for 30 years mainly as head of the Laboratory of Tumor Cell Biology. Gallo’s career would be dogged by controversy and misconduct allegations, but that’s a whole other article (stay tuned). The other career bureaucrat that would play a key role on the US side was none other than Anthony S Fauci, who recently completed a ridiculous 38-year reign as unelected head of the NIH's National Institute of Allergy and Infectious Diseases (NIAID). If you've surmised that, with names like the above, the HIV story must be a real shite show, you are absolutely correct. HIV is Invented 'Discovered' In 1983, the Pasteur Institute researchers declared they had 'isolated' a 'retrovirus' belonging to the family of T-cell leukemia viruses (HTLV), and concluded it "may be involved in several pathological syndromes, including AIDS." (Bold emphasis added) Their isolate came from a promiscuous 33-year-old Caucasian homosexual male referred to as "BRU", who indicated he'd had more than 50 sexual partners per year. Nasty. According to the authors, he displayed "signs and symptoms that often precede the acquired immune deficiency syndrome (AIDS)." However, the only symptoms reported for the patient were multiple lymphadenopathies (swollen lymph glands) and asthenia (weakness), which are evident in many conditions aside from AIDS. Neither fever nor recent loss of weight were noted. In other words, the patient from whom the alleged AIDS-causing virus was first 'isolated' from did not have an AIDS diagnosis. Tellingly, the patient did have a history of several episodes of gonorrhea and had been treated for syphilis in September 1982. Lymphadenopathy is one of the symptoms of both the aforementioned infections. The study's lead author was Francoise Barre-Sinoussi, although the finding is routinely credited to the paper's last listed author, the late Montagnier. The French study was marred by two key problems. It did not isolate any virus, and it did not show AIDS was caused by any HTLV offshoot. Forty years later, little has changed. The terminology and rationalizations have indeed become increasingly complex (as is the case with most elaborate lies), but there is no physical isolate of 'HIV.' Virologists and their sycophants, of course, insist this doesn't matter and that their non-purified mixtures are indeed isolates. While they condescendingly sneer and dismiss anyone who disputes this as a silly little dumb-dumb that doesn't 'understand' virology, they tend to remain rather quiet on another highly inconvenient observation. Namely, there is no proof that whatever is in their ‘isolates’ actually causes AIDS. HIV and Sars-Cov-2: The 'Deadly' Viruses That Aren't Deadly In the early days of 'COVID', testing positive for the mythical Sars-Cov-2 was considered a death sentence. So much so, that some folks didn't even bother getting their affairs in order; they instead killed themselves. Such is the power of all this heinous "deadly virus" bullshit. It was the same in the 'HIV' Dark Ages - testing positive was considered a death sentence. When a famous basketballer by the name of Erving “Magic” Johnson announced he was HIV positive in 1991, everyone was shocked. "Now we all know someone with HIV," said someone I can't recall in what was supposed to be a profound, insight-triggering moment. Johnson, everyone assumed, was now living on borrowed time. Thirty-three years later, Johnson is still alive and wealthy. He attributes his survival to antiretroviral cocktails that have never been shown in clinical studies to benefit survival: GlaxoSmithKline's Trizivir and Abbott's Kaletra. These cocktails are comprised of drugs like AZT which increase the risk of side effects but have never been shown to exert a mortality benefit. Johnson, it should be noted, has featured in ads for both products. In 2009, the FDA issued a warning letter to Abbott Laboratories regarding a promotional DVD in which Johnson discussed his experiences with Kaletra. The letter stated the violations were of public health concern "because they suggest that Kaletra is safer and more effective than has been demonstrated by substantial evidence or substantial clinical experience, and encourage use in circumstances other than those for which the drug has been shown to be safe and effective." "FDA is not aware of substantial evidence or substantial clinical experience to support effectiveness for five or more years of treatment with Kaletra in treatment-experienced adults. The personal experience of Kaletra patients, such as Magic Johnson, does not constitute such evidence." So if overpriced drug cocktails aren't keeping Johnson alive, what explains his survival? It's explained by the fact that HIV is a load of bollocks. A shady test that claims you are ‘HIV positive’ does not mean you are in fact harboring a deadly 'virus.' If ‘HIV’ was so deadly, then lab animals infected with it would get sick and die. But guess what? Administering a so-called isolate of uber-deadly HIV to animals results in ... nothing. Stugatz. That's right - directly administering the Virus That Causes AIDS™ to animals does not cause AIDS. "The only animals susceptible to experimental HIV-1** infection are the chimpanzee, gibbon ape, and rabbit but AIDS-like disease has not yet been reported in these species," lamented the authors of a 1989 FASEB paper. Oops. I'm guessing those chimps, gibbons and wascawwy wabbits didn't have a history of syphilis, smoking crack or inhaling poppers. Experiments in which human volunteers are deliberately 'infected' with the 'HIV isolate' would never get past the ethics committees of most research institutions. We do, however, have numerous instances of involuntary infection to give us a guide as to what happens when otherwise low-risk individuals are exposed to 'HIV.' In a 1984 NEJM letter, before 'HIV' testing became available, Sloan Kettering researchers reported there had been 27 parenteral exposures by 25 staff to the blood of AIDS patients since August 1982 (24 exposures were via needlestick). "All the involved staff are in their usual (generally excellent) state of health," including those who were exposed more than 12 months ago. Blood work was available for 12 staff with exposure more than 6 months prior, and no abnormalities were evident, reported the researchers. During 1985–2013, 58 confirmed and 150 possible cases of occupationally acquired HIV infection among healthcare workers were reported to the CDC. Since 1999, only one confirmed case (a laboratory technician sustaining a needle puncture while working with a live HIV culture in 2008) has been reported. There is no mention of subsequent AIDS, something the fear-porn agents at the CDC would surely have mentioned had it occurred. Some of you have probably heard of Dr Robert Willner, who twice deliberately pricked himself on TV with blood from 'HIV-positive' men (in Spain 1993, and USA 1994). Willner was an outspoken critic of the HIV hypothesis, having authored a book titled Deadly Deception: The Proof that Sex and HIV Absolutely Do Not Cause AIDS. Depending on who you listen to, Willner died 3 months after his 1994 TV appearance in a car crash, or the following year from a heart attack. Neither outcome is consistent with the oft-cited sequelae of AIDS. Jump, Jump, Jump Around Despite the fact that it is scientifically untenable, the HIV theory of AIDS still reigns supreme. Which brings us back to the key question: Why did 'HIV' wait until Wham! and Devine hit the charts before it started striking down gay blokes en mass? Enter the apes. According to Wikipedia, "HIV made the jump from other primates to humans in west-central Africa in the early-to-mid-20th century." (Bold emphasis added) Just like Sars-Cov-2 was purported to have kicked off when the allegedly zoonotic virus "jumped" to humans from a bat or pangolin at a Wuhan wet market that did not sell any bats or pangolins. Says Wikipedia, "Scientists generally accept that the known strains (or groups) of HIV-1 are most closely related to the simian immunodeficiency viruses (SIVs) endemic in wild ape populations of West Central African forests." (Bold emphasis added). "Generally accept" is code for "Scientists have no proof of this, but pretend it's true anyway." This brings us to an oft-cited 2011 paper titled "Origins of HIV and the AIDS Pandemic" which repeats the claim that "simian immunodeficiency viruses (SIVs) ... crossed from monkeys to apes and from apes to humans." The paper was authored by Paul Sharp and Beatrice Hahn, the latter a member of Gallo's NCI lab team which she joined in 1982. A chimpanzee minding his own business while a Gallo associate who blames apes for spreading HIV to humans (Beatrice Hahn) stares at him from a distance. In their paper, the researchers provide a graphic claiming SIV resulting in HIV-1 has been transmitted to humans via chimpanzees and gorillas. Hold that thought. According to the official narrative, the primary routes of 'HIV' transmission in humans are sexual intercourse with an infected individual, sharing needles with an infected person while taking drugs, transfusions of infected blood, or transmission from an infected pregnant mother to fetus. Sharp and Hahn speculate that SIVs first developed in chimpanzees, and were spread among the chimpanzee community primarily through sexual activity, from infected mothers to infants, and "in rare cases, possibly by aggression." But how did the disease "jump" from apes to humans? Researchers can't claim humans and apes were shooting up drugs together and sharing needles while doing so, or that apes were administering blood transfusions to humans, because that would be patently absurd. Ditto for suggesting apes were passing SIV to humans via birth, because apes don't give birth to humans. Claiming that apes transmitted SIV to humans because they were having cross-species sexual encounters would also be a hard sell. Humans are capable of some pretty weird and degenerate behaviour, but good luck pinning down a chimp or gorilla while you attempt to get jiggy with it. Meet Bruce. Can bench press you and your extended family with one arm. Incursions into his personal space not advised. "How humans acquired the ape precursors of HIV-1 groups M, N, O, and P is not known," write Sharp and Hahn, "however, based on the biology of these viruses, transmission must have occurred through cutaneous or mucous membrane exposure to infected ape blood and/or body fluids. Such exposures occur most commonly in the context of bushmeat hunting." (Bold emphasis added). Researchers can't explain exactly how immunodeficiency viruses pole-vaulted from apes to human, so they simply assume it must have happened during hunting expeditions. Virologists do a lot of assuming. Sharp and Hahn write that the first clue to HIV-1's "sudden emergence, epidemic spread, and unique pathogenicity" came in 1986 when a “morphologically similar but anti-genically distinct” virus was allegedly found to cause AIDS in patients in western Africa. Well riddle me this, Batman: Humans have been around for 2.5 million years, and the earliest Homo sapiens were getting around some 300,000 years ago. We've been hunting that whole time. Furthermore, the advance of agriculture and the steadily declining numbers of hunter-gatherers in modern times would have meant a greatly reduced opportunity for SIV to jump aboard the H-train via scratchy-bitey-fluid-exchangey hunting confrontations. Yet immunodeficiency viruses waited until the latter half of the Twentieth Century to successfully make the big cross-species jump? What an utter crock. Wikipedia admits "How the SIV virus would have transformed into HIV after infection of the hunter or bushmeat handler from the ape/monkey is still a matter of debate." Translated: There is no actual scientific evidence to support the claim that, after allegedly entering the human body, ‘SIV’ magically transformed into ‘HIV.’ The Sodomy Paradox There's another problem with the official AIDS narrative which holds that, after catching SIV from apes during hunting mishaps in Africa, it "transformed" into HIV, which hunter-gatherers then spread by doing the backdoor boogie with gay abandon. That story further holds that, somewhere along the way, one of these HIV-carrying ape-hunters nailed a gay airline steward from America. Patient Zero then flew back to the US, and began having lots of AIDS-causing unprotected sex in the saunas of San Francisco. Or the gay bars of New York. Or the wet markets of Wisconsin, I'm not sure, all this virus BS gets a bit hard to keep track of after a while. It doesn't really matter, because like the rest of the AIDS tale, the gay airline steward story was nonsense. Gaetan Dugas, the French-Canadian flight attendant posthumously labelled 'Patient Zero' and accused of single-handedly igniting the spread of HIV/AIDS across North America, was later exonerated. Thanks to the determined sleuthing of Pullitzer Prize-winning reporter John Crewdson, it was known by 1988 that what we now call AIDS was in fact present in America in the 1960s. While the rest of the media was tripping over itself to blame Dugas (“THE MAN WHO GAVE US AIDS” blared the New York Post’s October 6, 1987 headline; “Canadian Said to Have Had Key Role in Spread of AIDS,” wrote the New York Times, while the National Review nicknamed Dugas “the Columbus of AIDS"), Crewdson had discovered a 1973 case report that showed the official Patient Zero story was bollocks. That 1973 case report described Robert Rayford, a 15-year-old black lad from St. Louis who had died of AIDS in 1969 - more than a decade before anyone knew what AIDS was. The impoverished teen had presented to hospital in the spring of 1968 with swollen loins covered with open, infected sores. He struggled while breathing, was razor thin and pale as a ghost. Doctors initially suspected cancer, but subsequent tests revealed herpes, genital warts, and a severe case of chlamydia. The infection spread, in the form of purple colored lesions, to his legs, causing a misdiagnosis of lymphedema. He eventually succumbed to his condition in May 1969, leaving doctors baffled. The teen, who doctors described as mildly intellectually impaired, said he'd suffered the symptoms for around two years prior to seeking medical help. He denied injury or animal bites, had not travelled outside the midwestern United States, but admitted to "frequent" heterosexual intercourse. His family consented to an autopsy, which revealed "widespread Kaposi's sarcoma of the aggressive, disseminated type." The autopsy also found evidence of anal scarring and a particular kind of lesion no one had identified when Rayford was alive. Some doctors thought the scarring indicated Rayford was gay; others pointed out he may have been sexually abused. Struck by how closely Rayford's symptoms resembled those of AIDS, Crewdson flew to St. Louis and found a pathologist willing to dig through laboratory freezers in search of the youth's tissue samples. By using the test 'co-developed' by Gallo and the French, researchers were able to determine that the boy, incredibly, had been infected with 'HIV.' The finding was published in JAMA in 1988. However, it was not until 2016 that the fake Dugas tale was officially revoked. Had the Rayford story been more widely known, it wouldn’t have been good for HIV business. Not to worry, the out-of-Africa hypothesis was salvaged in 1998 when researchers claimed they had detected HIV - by a PCR process involving two rounds of amplification for a combined total of 69 cycles - in a plasma sample obtained in early 1959 from an adult Bantu male, with a sickle-cell trait and a glucose-6-phosphate-dehydrogenase deficiency, living in the Belgian Congo. Two of the researchers announcing this narrative-saving discovery hailed from the Aaron Diamond AIDS Research Center, at Rockefeller University in New York. So just like the COVID charade, we have a shamdemic for which the original Patient Zero story was shown to be a bunch of cobblers. Just like the COVID sham, few people noticed or cared and the rest of the AIDS tale continued its relentless march and took on a life of its own. Despite more holes than a ... wait, that's dangerous pun territory ... I mean, despite a plethora of discrepancies, the official Fauci-endorsed tale still has HIV migrating from Africa to the US and spread in the early 1980s by blokes bumping uglies in big city gay bars and saunas. And Fauci should know, because he went to gay saunas and gay bars himself in the “early stages” of the AIDS “explosion” to get a “feel” for the situation. Purely for ‘research’ purposes, of course (wink, wink). It's okay Tony, it's 2024, you don't have to cover for your sexuality anymore. A young Anthony Fauci displaying his "I've just been to the saunas!" smile. Your tax money at work. You could literally fill a book with all the discrepancies contained within the official AIDS story; several authors have already done just that. What I wanted to highlight here are the commonalities between the AIDS and COVID sagas. Both featured never-isolated 'viruses' with nonsensical 'Patient Zero' stories. ‘Isolates’ of both these ‘deadly’ and ‘novel’ viruses do a whole lot of nothing when administered to our primate cousins. Both sagas featured Anthony Fauci, showing up on cue touting the most toxic drug he could get away with recommending. Both featured doomsday, end-of-times hyperbole in which testing 'positive' was initially considered a death sentence. Both were remarkable demonstrations of how the media and masses could be easily manipulated into accepting a pandemic scare that, upon the most cursory examination, simply didn't add up. *During the presidency of former actor Ronald Reagan, senior administration officials secretly — and illegally — arranged for the sale of arms to Iran in return for Iran’s promise to help secure the release of a group of Americans being held hostage in Lebanon. Suspiciously, the hostages were formally released into US custody just minutes after Reagan was sworn into office. Proceeds from the arms sales were then secretly, and again illegally, funneled to the Contras, a group of rebels fighting the Marxist Sandinista government of Nicaragua. Is if that wasn't bad enough, the CIA looked the other way while the Contras trafficked cocaine into the US to help finance their fight to oust the communist Sandinistas. The scandal was exposed in 1996 by the brilliant, Pullitzer Prize-winning journalist Gary Webb while writing for the San Jose Mercury News. His series described a San Francisco Bay Area drug ring that sold tons of cocaine to the Crips and Bloods street gangs of Los Angeles, funelling millions in drug profits to the CIA-assisted Contras. This drug ring "opened the first pipeline between Colombia's cocaine cartels and the black neighborhoods of Los Angeles" and, as a result, "helped spark a crack explosion in urban America." His articles caused a proverbial shit-storm, prompting the government to conduct several investigations into itself and declaring itself innocent of all charges. We were supposed to believe it was all just an accidental oversight when even the Kerry report acknowledged "the Contra drug links included", among other connections, "... payments to drug traffickers by the U.S. State Department of funds authorized by the Congress for humanitarian assistance to the Contras, in some cases after the traffickers had been indicted by federal law enforcement agencies on drug charges, in others while traffickers were under active investigation by these same agencies." (Bold emphasis added). The Los Angeles Times, New York Times, and Washington Post launched their own 'investigations' (read: hatchet jobs) and rejected Webb's allegations, instead siding with the government - a practice they uphold to this day. However, an internal CIA report released in 1998 admitted the CIA ‘overlooked’ or ‘ignored’ reports that the Nicaragua Contra rebels financed their fight to oust the communist Sandinistas through the sale of drugs in the United States. **‘HIV-1’ is the form of ‘HIV’ allegedly most common and threatening to humans. According to the official tale, ‘HIV-2’ is rare and of little threat. Share https://substack.com/home/post/p-146567752
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    Why the Official AIDS Story is a Complete Crock
    The Great Rebranding, 1980s-Style: HIV Was a Sham, Just Like Sars-Cov-2
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  • EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed
    “I already have had.. uh.. patients die from shedding” - Ana Maria Mihalcea, M.D.

    Dr. Ariyana Love (ND)
    “My people are destroyed for lack of knowledge: because thou hast rejected knowledge, I will also reject thee, that thou shalt be no priest to me: seeing thou hast forgotten the law of thy God, I will also forget thy children.” ~ Hosea 4:6 KJV

    Rockefeller Medicine

    Around 1900, the science world was getting excited about new “petrochemicals” and the ability to create a variety of new compounds from oil. Some of the first products derived from petrochemicals were plastics.

    In 1908, modern medicine was established by the Rockefeller’s and dubbed “Allopathy”. The Rockefeller’s created the business of modern medicine which has always been about poisoning people, Eustice Mullen explains.

    This is the definition of Allopathic medicine according to the NIH:

    “A system in which medical doctors and other health care professionals (such as nurses, pharmacists, and therapists) treat symptoms and diseases using drugs, radiation, or surgery.”

    The Rockefeller Institute for Medicine, founded in 1908, marked the advent of the re-creation of synthetic versions of natural cures. Prior to 1908, every place of healing in America, Europe and the world, used only ancient traditional natural medicinal cures. Every hospital was a “Homeopathic Hospital”. Most of these magnificent buildings were converted into mental health asylums where a system of torture and electric shock was established to “cure” mental illness.


    John D. Rockefeller created the oil industry and used it to crush traditional medicine in order to enslave people. They also financed the Eugenics movement. One of the perks of modern medicine is depopulation.

    “Everyone knows that the infamous Roe v. Wade opinion legalized abortion, but almost no one knows that legal abortion was a strategy by eugenicists, as early as 1939, to “genetically improve” the population by “reducing” it.”

    In the book, “Rockefeller Medicine Men: Medicine and Capitalism in America”, authored by E. Richard Brown, he tells the hidden story of the financial, political, and institutional manipulations whereby a diverse and eclectic range of traditional healing modalities available to the North American public was summarily canceled and pared down to a singular style of medicine that would become the predominant medicine of the Western world and a major force in global medical culture during the 20th century. This was brought about largely by the collaboration of the American Medical Association, the philanthropies of Andrew Carnegie and John D. Rockefeller, and the development of a revolutionary curriculum by the Johns Hopkins School of Medicine. Brown documents the story of how a powerful professional elite gained virtual hegemony in the Western theatre of healing by effectively taking control of the ethos and practice of Western medicine. E. Richard Brown describes how, in 1905, the American Medical Association’s new Council on Medical Education funded by Carnegie and Rockefeller commenced serious activity. They employed the services of Abraham Flexner who proceeded to visit and “assess” every single medical school in the US and Canada. Within a short time of this development, medical schools all around the US began to collapse or consolidate. By 1910, 30 schools had merged, and 21 had closed their doors. Of the 166 medical schools operating in 1904, 133 had survived by 1910, and 104 by 1915. Fifteen years later, only 76 schools of medicine existed in the US and they all followed the same curriculum.

    The 1910 Flexner Report laid the foundations of the modern medical system, dubbed “Rockefeller medicine” (Allopathy). Since 1910, corporate interests have established near total control of the medical field, both though pharmacology and through their impact on medical education.

    In 1935, vitamin C became the first vitamin to be artificially synthesized in Switzerland. Rockefeller saw a big opportunity with the possibility that vitamins and medications could be developed from petroleum. He saw the chance to control and monopolize multiple industries at once: petroleum, chemical and medical. Petrochemicals were ideal from a business perspective because they could be patented, owned and sold for high profits.

    Today, the petrochemicals in plastics are causing a slew of illnesses including neurodevelopmental disorders, diabetes, chronic respiratory disease, and cancer, which have increased between 28% and 150% between 1990 and 2019. Petrochemicals in microplastics are also rapidly reducing fertility in males in particular, and polluting our environment. Please also read more here, here, and here.

    The first pharmaceutical drug was an arsenic named Salvarsan. That’s right, an ARSENIC!

    DEATH is an all-to-common side effect of pharmaceutical drugs which is only logical when you administer poisons internally. The following pages demonstrate the many deaths of people around the world, most of them children, who were fatally poisoned during the first mass medication experiments with Rockefeller’s Allopathic health. The paper is entitled, Toward Responsibility in International Health: Death following Treatment in Rockefeller Hookworm Campaigns, 1914–1934.

    What is EDTA?

    EDTA is synthesized on an industrial scale using 1, 2-diaminoethane (ethylene diamine), formaldehyde, water and sodium cyanide.

    Ethylene diamine induced acute and subchronic toxicity in lab animals, also allergic hypersensitivity. The liver and kidneys are target organs of ethylenediamine, where they simply stop working.


    Read more: Is C60 And EDTA Safe? Clinical Review


    Absorption of large amounts of formaldehyde via any route can cause severe systemic toxicity, leading to metabolic acidosis, tissue and organ damage, and coma, according to the CDC.

    Exposure to sodium cyanide can be rapidly fatal. It has whole-body (systemic) effects, particularly affecting those organ systems most sensitive to low oxygen levels: the central nervous system (brain), the cardiovascular system (heart and blood vessels), and the pulmonary system (lungs), according to the CDC.

    EDTA is an industrial poison. The textile industry required a chelating agent to remove calcium during textile processing and this led to the synthesis of polyamino-carboxylic acids, one of which was EDTA. A patent was filed for EDTA in Germany in 1935, for industrial chemical use. EDTA is a synthetic acid effectively used to clean boiler rooms in nuclear power plants. In 1945, Franz Munz obtained a US EDTA patent in 1945. In 1947, EDTA was approved by the US Food and Drug Administration (FDA) as a food additive in “low doses” because it’s a forever chemical and a preservative.

    There are two different types of EDTA approved by the U.S. FDA. In 1953, Edetate calcium disodium also known as Calcium EDTA (marketed under the trade name Calcium Disodium Versenate registered ) was approved for the treatment of lead poisoning. Three years later, in 1956, a related EDTA compound, Edetate disodium, was also approved for clinical use. This compound, also known as Disodium EDTA, has been marketed under the trade names Disotate (registered) and Endrate (registered). The essential difference between these two compounds is that Calcium EDTA's structure has an incorporated Ca super(2+) moiety while Disodium EDTA does not. The use of the latter compound, Disodium EDTA, has been associated with life-threatening and fatal hypocalcemia.

    EDTA trial DEATHS

    An EDTA trial (Sloth-Nielsen et al., 1981) on the possible antiatherogenic effect of EDTA with 6 patients, showed clinical signs of potentially lethal hypocalcemia from abnormally low calcium levels caused by EDTA.

    Another EDTA chelation human trial in 2003-2005 resulted in DEATHS due to hypocalcemia.

    A 2006 EDTA chelation trial also resulted in DEATHS due to hypocalcemia.

    There were several DEATHS reported from cardiac arrest due to lethal hypocalcemia in EDTA trials in 2006 and 2008 and (Brown, Willis, Omalu, & Leiker, 2006; Baxter & Krenzelok, 2008), from calcium deficiency inducing alterations in the brain, and osteoporosis, which causes the bones to become brittle.

    In 2008, a clinical trial with EDTA chelation on autistic children also proved fatal, resulting in DEATHS of children.

    A 2007 EDTA chelation study proved KIDNEY FAILURE in humans.

    Decades of clinical studies demonstrate that EDTA treatment is associated with severe, life-threatening adverse effects, as Science Direct explained in 2016.

    “It should be emphasized that EDTA treatment is associated with severe, life-threatening adverse effects.

    EDTA for cardiovascular disease DEBUNKED

    Many Allopathic specialists tried to popularize the use of EDTA for chelation, to no avail. In the 1980s, Richard Casdorph, a practicing cardiologist, claimed improvements in ejection fractions of the heart and in cerebral blood flow with EDTA chelation therapy in several articles. McDonagh, Rudolph, and Cheraskin published about 30 articles documenting various positive effects of EDTA chelation. This group wrote articles showing no problems with kidney function in patients treated with EDTA according to the published protocol. At the same time, conventional cardiologists wrote several editorials against EDTA chelation. So the American Medical Association called for studies to see if chelation worked. The American Board of Chelation Therapy in 1983 was formed to certify doctors who give the therapy. It was later called the American Board of Clinical Metal Toxicology. ACAM also certified doctors who took its workshop on chelation therapy and passed its written and oral examinations. The Great Lakes College of Clinical Medicine, later called the International College of Integrative Medicine (ICIM), was formed in 1983 to teach and do research on chelation and other integrative therapies. After complex negotiations, in the late 1980's Walter Reed Army Hospital agreed to do a randomized clinical trial on EDTA chelation therapy, but part way through the study it was suddenly discontinued for unknown reasons.

    However, in a paper by Seely, Wu, and Mills, (2005), a systematic review of published articles in this field was undertaken. The authors concluded that the best current available evidence did not support the therapeutic use of EDTA chelation therapy in the treatment of cardiovascular disease. Similar results have been reported in review papers by Shrihari, Roy, Prabhakaran, and Reddy (2006) and Crisponi et al. (2015).

    While a 2002 EDTA large randomized clinical trial “showed benefit”, smaller studies were inconsistent.

    In the 1990s, the Federal Trade Commission filed a complaint against ACAM for making a claim in a brochure that chelation was effective for vascular disease. ACAM submitted almost 100 articles in support of the claim, but the FTC insisted that a large randomized trial was required to make that claim. ACAM finally gave up after spending a million dollars in legal fees and signed a consent order saying they would not make such a claim anymore, based on the evidence at that time.

    In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up.

    A slew of other adverse events such as lacrimation, nasal congestion, mucocutaneous lesions, glycosuria, hypotension, and ECG abnormalities (DISEASE OF THE HEART AND LUNGS) have also been reported as well as allergic reactions (Wax, 2013) to EDTA. Prolonged treatment with calcium EDTA gives rise to depletion of magnesium and trace-metal depletion, the most marked being due to the excretion of zinc. Zinc depletion destroys your cells’ ability to absorb nutrients and leads to diabetes.

    A 2015 study entitled, Quality of Life Outcomes with a Disodium EDTA Chelation Regimen for Coronary Disease: Results from the TACT Randomized Trial concluded with this statement:

    “In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up.”

    Severe kidney damage from EDTA chelation therapy was reported in a (Nissel 1986) trial. In a very short period of time, EDTA causes kidneys to shut down in complete failure.

    A study from 2015 suggests EDTA chelation for myocardial infarction with “modest” benefits to cardio health. However, I would suggest that the moderate benefits of this study were due to the high doses of vitamin C administered.

    A 2017 study on EDTA chelation for atherosclerosis and Miocardial Infraction concluded:

    “Unsubstantiated claims of chelation therapy as an effective treatment of atherosclerosis should be avoided and patients made aware of the inadequate evidence for efficacy and potential adverse effects, especially the harm that can occur if used as a substitute for proven therapies.”

    In a 2018 EDTA trial it was concluded:

    “These results… are not sufficient to support the routine use of chelation therapy for treatment of patients who have had an MI (Miocardial Infraction)”.

    A study from 2023 entitled, Chelation Therapy Associated with Antioxidant Supplementation Can Decrease Oxidative Stress and Inflammation in Multiple Sclerosis: Preliminary Results proved a flop with two participants discontinuing their trial participation.

    EDTA for lead poisoning DEBUNKED

    EDTA has also been touted as a treatment for lead poisoning. Because of its adverse effects, calcium EDTA was replaced by DMSA in the treatment of lead poisoning (Aposhian et al., 1995) in 1995. CaEDTA has also been used for the treatment of cases with manganese toxicity, but the result was neurotoxic symptoms resembling PARKINSONISM (Andersen, 1999).

    A 2004 trial showed that EDTA actually REDISTRIBUTES LEAD TO THE BRAIN after acute or chronic lead exposure (Andersen, 2004).

    Another trial proved adverse effects in 5 patients receiving EDTA at an outpatient chelation clinic in 2002, and all patients experienced gastrointestinal and musculoskeletal symptoms.

    Oral exposure to EDTA (2002) had produced adverse reproductive and developmental effects in animals. EDTA did not make it past the animal or human trials, so why are medical doctors using it in humans?

    A 2002 EDTA trial was performed on humans as a test for “chelation” therapy by a chelation clinic, demonstrating adverse events in 5 out of 5 patients.

    Additionally, EDTA is a persistent organic pollutant (POP). In that case, each intake would only be partially excreted, while the remaining chemicals build up in the body and produce cell death. And long-term exposure to calcium disodium EDTA creates toxicity and kidney damage.

    EDTA Snakeoil Salesmen

    In March 2023, Ana Maria Mihalcea interviewed Dr. Michael Roth who claims that EDTA is a “synthetic amino acid related to vinegar.” Together they make a slew of medical claims that are not scientifically proven, such as that EDTA “detoxifies covid vaccine, heavy metals, graphene oxide, parasites, hydrogels, and nanoparticles”.

    The only scientific tool Ana Maria uses to back her claims is dark field microscopy. You cannot see nanoparticles with a dark field microscope. It takes a spectroscopy microscope to identify nanoparticles. Her medical claims are simply fabricated and unscientific lies.

    Ana Maria and Dr. Ross made additional unproven medical statements that “EDTA removes the effects of a heart attack, can bring back the elderly from senility and Alzheimer’s, reduces blood pressure, detoxifies several snake and spider venoms, lowers insulin, smooths skin and wrinkles, ” and a host of other laughable health claims that aren’t backed by anything.

    Incidentally, Dr. Ross is now dead.

    “Dr. Roth sadly passed away on March 11/2023”


    My sources informed me that Dr. Rashid Buttar was using EDTA. Given that he was already severely poisoned as Stew Peter’s reported, using EDTA Acid would have been enough to tip him over the edge and kill him.

    EDTA is not an approved pharmaceutical drug. It was Covid Emergency approved by the FDA under an Emergency Use Authorization (EUA), just like the modified RNA (modRNA) Covid-19 vaccine nanotechnology.

    The National Center for Complementary and Integrative Health (.gov) makes it clear that the use of EDTA chelation for heart disease has not been approved by the FDA.

    Ana Maria has been touting EDTA as an “antioxidant” when it is not. She even published to her Substack that EDTA is an “Antioxidant” when in fact it’s an acid poison and an oxidant. Many people saw it on her Substack before she removed it.

    I’ve had over a dozen clients come to me extremely sick from EDTA pills and EDTA IV infusion. Some told me they thought it was a natural substance due to Ana Maria’s false advertising and medical malfeasance. A Medical Doctor is licensed to know wether EDTA Acid is an oxidant poison or an antioxidant. Not knowing this and inducing the death of a patient is not an acceptable excuse. Ana Maria is criminally liable.


    EDTA is an oxidant when used internally. The studies that refer to EDTA as an “antioxidant” are in vitro lab studies, not in vivo (inside the body).

    EDTA is used to preserve cell specimens for chemistry lab work because it prevents blood coagulation and oxidation of cells in a petri dish where it’s used for diagnostic purposes. This is the kind of “antioxidant” the studies are referring to. But when you infuse EDTA Acid into the human body, it acts as an oxidant poison.

    EDTA also will not decoagulate the blood in vivo (inside the body). But I can see how people who cannot read peer-reviewed literature could be deceived and manipulated by snake oil salesmen.

    For example, a study entitled, “Comparative study of the antioxidant capability of EDTA and Irganox”. EDTA is a preservative used in laboratories to preserve cells for scientific lab research. EDTA prevents the oxidation of cells in a petri dish. Oxygen causes cells to deteriorate, but labs need them to last longer for research purposes. When used inside the human body (in vivo), it’s a different story. Then EDTA acts as an oxidant poison, not an antioxidant. So this has a very different meaning.

    One of the well documented and widely known adverse events from EDTA “chelation” is DEATH, according to Mount Sinai.

    Other serious side effects that have been reported include low blood sugar, diminished calcium levels, headache, nausea, dangerously low blood pressure, kidney failure, organ damage, irregular heartbeat, seizures, or even death.

    I have to wonder if Ana Maria Mihalcea is informing her patients that death is a potential adverse event to EDTA chelation? In a March 24, 2024, broadcast that Ana Maria released, at the 53:24 minute mark, she makes a chilling confession:

    “I already have had… uh… patients die from the shedding”

    How many of Ana Maria Mihalcea’s patients have been killed by her EDTA infusion protocol? I was horrified when I heard Ana Maria’s confession because I haven’t had any clients die from shedding! I’ve treated many people who were extremely sick from shedding, and I helped them all to detox effectively. Some clients came to me after several hospitalizations from extreme shedding but none of them died in my care! Nobody needs to die from shedding if they use an effective detox protocol.

    Between 1-2 years, Ana Maria has been claiming that EDTA detoxes graphene, dissolves graphene and chelates heavy metals, but experts such as Dr. Robert Young and Dr. Judy Mikovitz told me this is impossible.

    Ana Maria has gone so far as to produce a medical study with unscientific claims right in the title, “EDTA Chelation Dissolves the Artificial Intelligence Magnetic Hydrogel Weapon”. The study was also promoted by Health Canada. In her study, Ana Maria claims that EDTA can “detoxify the body even from Graphene”.

    EDTA is not a detox agent! Again, it’s an oxidant that degrades cells whereas genuine antioxidants repair cells.

    Ana Maria does in fact know about oxidant poisons. In an interview from December 2022, she referred to graphene as an oxidant. At least she’s correct about something.

    Saul Green, Ph.D., and Wallace I. Sampson, M.D. wrote in great detail about the Implausibility of EDTA Chelation Therapy, stating:

    “EDTA chelation effectiveness is implausible; (2) the preponderance of evidence shows ineffectiveness; and (3) EDTA augments oxidative reactions involving iron instead of inhibiting them, resulting in increased likelihood of production of oxygen free radicals rather than neutralization of them, as claimed.”

    EDTA a precurser to cellular transfection

    The Rockefeller Institue of Medicine has done clinical research on EDTA. One particular study entitled, Studies of Cell Deformity from 1967, shows that cells will degrade from EDTA exposure, which also induces “deformation” on their surfaces. The trial demonstrated that EDTA stops cellular synthesis of calcium. They learned that calcium is bound to anionic sites at the cell periphery, some of which are located at the cellular electrokinetic surface.

    Due to Rockefeller’s research, EDTA is now used in electrophoresis which is a laboratory technique used to separate DNA, RNA or protein molecules based on their size and electrical charge. An electric current is used to move the molecules through a gel or other matrix, according to the National Human Genome Research Institute.

    In agarose gel electrophoresis, EDTA is added for chelating the magnesium ions which are cofactors for DNA nucleases. Hence, activity of DNA nucleases that may be present is inhibited, and “DNA is protected from degrading”. This is why EDTA is an effective transfection agent because it dissolves parts of your DNA, preserving cells for lab research in vitro.

    Gel electrophoresis using EDTA is routinely used for detection and size analysis of proteins and nucleic acid. DMSO is used with EDTA in this process. This destruction of cells makes transfection (gene editing) of cells easier using CRISPR-Cas9 which splices and dices the genome in vivo, as this study explains entitled, “Inhibition of CRISPR-Cas9 ribonucleoprotein complex assembly by anti-CRISPR AcrIIC2”.


    EDTA was found to be genotoxic in laboratory animals. A study from 1983 demonstrates that EDTA induces gene mutations and chromosomal breakage, meaning that genetic mutations will be passed on your offspring, affecting generations to come, according to this Genetic Toxicology of EDTA study from 1983.

    Calcium chelate of EDTA (CaEDTA) “chelation” has shown teratogenic effects (Catsch & Harmuth-Hoene, 1976), which are central nervous system depression and peripheral neuropathy. EDTA produced abnormalities in pups of rats removed by cesarian section on day 21 of the study. Increases in several abnormalities (cleft palate, adactyly or syndactyly, abnormal rib or abnormal vertebrae) were observed with increased doses of CaEDTA.

    EDTA improves transfection of embryonic stem cells lines (hESC) in cells, according to the NIH.

    According to a peer reviewed paper from the NIH, EDTA is a precursor to cellular transfection.

    “We found that chemically abrading the differentiated CACO-2 human intestinal epithelial cell layer by a trypsin and EDTA pretreatment (before the use of detergent-like transfection reagents) dramatically improved transfection efficiency in this polar, differentiated model. Although this treatment did improve the transfection efficiency, it also induced leakiness in the epithelial barrier by both opening tight junctional complexes and by creating holes in the cell layer because of low-level cell death and detachment. Thus, this approach to enhance the transfection efficiency of polar, differentiated cells will be useful for assessment of the effect of the transfected/expressed protein on (re)formation of an epithelial barrier..."

    Thermo Fisher Scientific Inc. Fetal Bovine Serum for human transfection also uses EDTA.


    An NIH study entitled, “Kinetic Basis for DNA Target Specificity of CRISPR-Cas12a” reveals that EDTA enables rapid binding to DNA during gene editing (transfection).

    Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” explains:

    “CAS12a is an RNA-guided, programmable genome editing enzyme found within bacterial adaptive immune pathways. Unlike CRISPR-Cas9, Cas12a uses only a single catalytic site to both cleave target double-stranded DNA (dsDNA) (cis-activity) and indiscriminately degrade single-stranded DNA (ssDNA) (trans-activity).”

    According to the study, “A DNA loading buffer of 45% formamide and 15 mM EDTA, with a trace amount of xylene cyanol and bromophenol blue…” is used to transfect the human genome.

    So, EDTA is a transfection agent used with CRISPR-Cas9 to edit the human genome. Does EDTA actually dissolve graphene, as Ana Maria claims? The answer is NO! EDTA oxidant is used to reduce graphene to Reduced Graphene Oxide (RGO) form. Graphene is reduced by oxidation. Rather than dissolving graphene, EDTA reduces it to Graphene Oxide Nanoparticles otherwise known as Quantum Dots.

    Graphene oxide is more toxic than graphene, as I documented in my article entitled, “Graphene Oxide The Vector For Covid-19 Democide”.

    I will emphasize again that Graphene Oxide Quantum Dots cannot be seen with a dark field microscope. So Ana Maria’s claims that EDTA is detoxing graphene from the human body is unscientific.

    EDTA chelation for graphene nanocomposites

    EDTA chelation is NOT effective in removing metals from the human body. It's actually a different kind of chelation that’s used to create electrochemical sensors (biosensors) when combined with GRAPHENE!

    EDTA serves as a connecting mediator between NiHCF (Graphene Oxide Nanoparticles and Nickle) and graphene nanosheets. EDTA is used with metal nanoparticles, metal oxides, graphene, carbon nanotubes, and quantum dots to stabilize the technology for a more uniform distribution throughout the body.

    A Science Direct paper entitled, “Highly sensitive ascorbid acid sensors from EDTA chelation derived nickel hexacyanoferrate/graphene nanocomposites” reveals that EDTA is used to create Graphene/Nickel, AA sensor nanocomposites.

    “EDTA chelation stragey” is used for the “homogeneously distrubuted" NiHCF” (Nickel hexacyanoferrate composite) on graphene sheets. EDTA residue-supported pyramidal and spherical nanoparticles of NiHCF deposited on graphene sheets is used to create biosensors for the formation of Graphene/Nickel hydrogels.


    The graphene hydrogel nanocomposite sensors (Gr/NiHCF) are used as externally controlled biosensing tools. They tell us it’s used to test for ascorbic acid, but the application of this technology is for “human life” as well as for industrial use. See link here.


    Graphene oxide/Lauric acid nanoparticles are modified using EDTA. Lauric acid nanoparticles is suggested as a “prospective drug carrier” for oral nanoparticle-mediated sustained drug delivery (timed release technology) used for the removal of Pb(II) ions (lead). However, studies show there are cytotoxic results.

    Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” demonstrates how EDTA improves transfection and modification of the human genome.

    Once Graphene is reduced to Graphene Oxide, due to its small particulate size, you can no longer identify it using a Dark Field Microscope. Ana Maria is using a dark field scope, not a spectroscopy microscope, which is the only instrument that can measure GON and Quantum Dots.

    So what is Ana Maria doing with EDTA infusions? She’s creating a metal-EDTA complex that stabilizes and strengthens the graphene-based nanotech weapon system and enables it to spread more readily throughout the body, for human transfection. She uses “light and sound healing techniques” to activate the delayed release technology before administering EDTA infusion, as she reveals in an interview here.

    EDTA is a poison acid that dissolves DNA. It's used to prime the cells’ DNA for transfection. EDTA disrupts the surface of skin cells so that other chemicals can penetrate more easily and CRISPR-Cas9 gene editing technology can work more efficiently.

    The NIH describes EDTA’s enhanced cellular transfection:

    “Flow cytometric analysis using an enhanced green fluorescent protein vector showed a significantly increased transfection efficiency of EDTA method compared to standard enzyme method. In addition, the EDTA approach maintained stable cell viability and recovery rate of hESCs after transfection.”

    Another study published in Research Gate, confirms that EDTA increases cellular transfection, along with using chloroquine.

    Graphene Oxide Quantum Dots (GOQD-HA) nanocomposite use EDTA for tissue-specific delivery of Metformin, an anti-diabetic drug otherwise known as insulin.


    Conclusion

    Beware of snakeoil salesmen! Never trust pharmaceuticals! Superior heavy metal chelation supplements exist such as ASEA redox molecules and Master Peace, sign up and order here. Medicines made from nature are always superior to pharmaceutical drugs. Finally, be sure your Naturopathic Doctor is competent!

    Schedule a health consultation with me for a customized detox protocol and complete cellular health restoration.

    https://substack.com/home/post/p-144979143
    EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed “I already have had.. uh.. patients die from shedding” - Ana Maria Mihalcea, M.D. Dr. Ariyana Love (ND) “My people are destroyed for lack of knowledge: because thou hast rejected knowledge, I will also reject thee, that thou shalt be no priest to me: seeing thou hast forgotten the law of thy God, I will also forget thy children.” ~ Hosea 4:6 KJV Rockefeller Medicine Around 1900, the science world was getting excited about new “petrochemicals” and the ability to create a variety of new compounds from oil. Some of the first products derived from petrochemicals were plastics. In 1908, modern medicine was established by the Rockefeller’s and dubbed “Allopathy”. The Rockefeller’s created the business of modern medicine which has always been about poisoning people, Eustice Mullen explains. This is the definition of Allopathic medicine according to the NIH: “A system in which medical doctors and other health care professionals (such as nurses, pharmacists, and therapists) treat symptoms and diseases using drugs, radiation, or surgery.” The Rockefeller Institute for Medicine, founded in 1908, marked the advent of the re-creation of synthetic versions of natural cures. Prior to 1908, every place of healing in America, Europe and the world, used only ancient traditional natural medicinal cures. Every hospital was a “Homeopathic Hospital”. Most of these magnificent buildings were converted into mental health asylums where a system of torture and electric shock was established to “cure” mental illness. John D. Rockefeller created the oil industry and used it to crush traditional medicine in order to enslave people. They also financed the Eugenics movement. One of the perks of modern medicine is depopulation. “Everyone knows that the infamous Roe v. Wade opinion legalized abortion, but almost no one knows that legal abortion was a strategy by eugenicists, as early as 1939, to “genetically improve” the population by “reducing” it.” In the book, “Rockefeller Medicine Men: Medicine and Capitalism in America”, authored by E. Richard Brown, he tells the hidden story of the financial, political, and institutional manipulations whereby a diverse and eclectic range of traditional healing modalities available to the North American public was summarily canceled and pared down to a singular style of medicine that would become the predominant medicine of the Western world and a major force in global medical culture during the 20th century. This was brought about largely by the collaboration of the American Medical Association, the philanthropies of Andrew Carnegie and John D. Rockefeller, and the development of a revolutionary curriculum by the Johns Hopkins School of Medicine. Brown documents the story of how a powerful professional elite gained virtual hegemony in the Western theatre of healing by effectively taking control of the ethos and practice of Western medicine. E. Richard Brown describes how, in 1905, the American Medical Association’s new Council on Medical Education funded by Carnegie and Rockefeller commenced serious activity. They employed the services of Abraham Flexner who proceeded to visit and “assess” every single medical school in the US and Canada. Within a short time of this development, medical schools all around the US began to collapse or consolidate. By 1910, 30 schools had merged, and 21 had closed their doors. Of the 166 medical schools operating in 1904, 133 had survived by 1910, and 104 by 1915. Fifteen years later, only 76 schools of medicine existed in the US and they all followed the same curriculum. The 1910 Flexner Report laid the foundations of the modern medical system, dubbed “Rockefeller medicine” (Allopathy). Since 1910, corporate interests have established near total control of the medical field, both though pharmacology and through their impact on medical education. In 1935, vitamin C became the first vitamin to be artificially synthesized in Switzerland. Rockefeller saw a big opportunity with the possibility that vitamins and medications could be developed from petroleum. He saw the chance to control and monopolize multiple industries at once: petroleum, chemical and medical. Petrochemicals were ideal from a business perspective because they could be patented, owned and sold for high profits. Today, the petrochemicals in plastics are causing a slew of illnesses including neurodevelopmental disorders, diabetes, chronic respiratory disease, and cancer, which have increased between 28% and 150% between 1990 and 2019. Petrochemicals in microplastics are also rapidly reducing fertility in males in particular, and polluting our environment. Please also read more here, here, and here. The first pharmaceutical drug was an arsenic named Salvarsan. That’s right, an ARSENIC! DEATH is an all-to-common side effect of pharmaceutical drugs which is only logical when you administer poisons internally. The following pages demonstrate the many deaths of people around the world, most of them children, who were fatally poisoned during the first mass medication experiments with Rockefeller’s Allopathic health. The paper is entitled, Toward Responsibility in International Health: Death following Treatment in Rockefeller Hookworm Campaigns, 1914–1934. What is EDTA? EDTA is synthesized on an industrial scale using 1, 2-diaminoethane (ethylene diamine), formaldehyde, water and sodium cyanide. Ethylene diamine induced acute and subchronic toxicity in lab animals, also allergic hypersensitivity. The liver and kidneys are target organs of ethylenediamine, where they simply stop working. Read more: Is C60 And EDTA Safe? Clinical Review Absorption of large amounts of formaldehyde via any route can cause severe systemic toxicity, leading to metabolic acidosis, tissue and organ damage, and coma, according to the CDC. Exposure to sodium cyanide can be rapidly fatal. It has whole-body (systemic) effects, particularly affecting those organ systems most sensitive to low oxygen levels: the central nervous system (brain), the cardiovascular system (heart and blood vessels), and the pulmonary system (lungs), according to the CDC. EDTA is an industrial poison. The textile industry required a chelating agent to remove calcium during textile processing and this led to the synthesis of polyamino-carboxylic acids, one of which was EDTA. A patent was filed for EDTA in Germany in 1935, for industrial chemical use. EDTA is a synthetic acid effectively used to clean boiler rooms in nuclear power plants. In 1945, Franz Munz obtained a US EDTA patent in 1945. In 1947, EDTA was approved by the US Food and Drug Administration (FDA) as a food additive in “low doses” because it’s a forever chemical and a preservative. There are two different types of EDTA approved by the U.S. FDA. In 1953, Edetate calcium disodium also known as Calcium EDTA (marketed under the trade name Calcium Disodium Versenate registered ) was approved for the treatment of lead poisoning. Three years later, in 1956, a related EDTA compound, Edetate disodium, was also approved for clinical use. This compound, also known as Disodium EDTA, has been marketed under the trade names Disotate (registered) and Endrate (registered). The essential difference between these two compounds is that Calcium EDTA's structure has an incorporated Ca super(2+) moiety while Disodium EDTA does not. The use of the latter compound, Disodium EDTA, has been associated with life-threatening and fatal hypocalcemia. EDTA trial DEATHS An EDTA trial (Sloth-Nielsen et al., 1981) on the possible antiatherogenic effect of EDTA with 6 patients, showed clinical signs of potentially lethal hypocalcemia from abnormally low calcium levels caused by EDTA. Another EDTA chelation human trial in 2003-2005 resulted in DEATHS due to hypocalcemia. A 2006 EDTA chelation trial also resulted in DEATHS due to hypocalcemia. There were several DEATHS reported from cardiac arrest due to lethal hypocalcemia in EDTA trials in 2006 and 2008 and (Brown, Willis, Omalu, & Leiker, 2006; Baxter & Krenzelok, 2008), from calcium deficiency inducing alterations in the brain, and osteoporosis, which causes the bones to become brittle. In 2008, a clinical trial with EDTA chelation on autistic children also proved fatal, resulting in DEATHS of children. A 2007 EDTA chelation study proved KIDNEY FAILURE in humans. Decades of clinical studies demonstrate that EDTA treatment is associated with severe, life-threatening adverse effects, as Science Direct explained in 2016. “It should be emphasized that EDTA treatment is associated with severe, life-threatening adverse effects. EDTA for cardiovascular disease DEBUNKED Many Allopathic specialists tried to popularize the use of EDTA for chelation, to no avail. In the 1980s, Richard Casdorph, a practicing cardiologist, claimed improvements in ejection fractions of the heart and in cerebral blood flow with EDTA chelation therapy in several articles. McDonagh, Rudolph, and Cheraskin published about 30 articles documenting various positive effects of EDTA chelation. This group wrote articles showing no problems with kidney function in patients treated with EDTA according to the published protocol. At the same time, conventional cardiologists wrote several editorials against EDTA chelation. So the American Medical Association called for studies to see if chelation worked. The American Board of Chelation Therapy in 1983 was formed to certify doctors who give the therapy. It was later called the American Board of Clinical Metal Toxicology. ACAM also certified doctors who took its workshop on chelation therapy and passed its written and oral examinations. The Great Lakes College of Clinical Medicine, later called the International College of Integrative Medicine (ICIM), was formed in 1983 to teach and do research on chelation and other integrative therapies. After complex negotiations, in the late 1980's Walter Reed Army Hospital agreed to do a randomized clinical trial on EDTA chelation therapy, but part way through the study it was suddenly discontinued for unknown reasons. However, in a paper by Seely, Wu, and Mills, (2005), a systematic review of published articles in this field was undertaken. The authors concluded that the best current available evidence did not support the therapeutic use of EDTA chelation therapy in the treatment of cardiovascular disease. Similar results have been reported in review papers by Shrihari, Roy, Prabhakaran, and Reddy (2006) and Crisponi et al. (2015). While a 2002 EDTA large randomized clinical trial “showed benefit”, smaller studies were inconsistent. In the 1990s, the Federal Trade Commission filed a complaint against ACAM for making a claim in a brochure that chelation was effective for vascular disease. ACAM submitted almost 100 articles in support of the claim, but the FTC insisted that a large randomized trial was required to make that claim. ACAM finally gave up after spending a million dollars in legal fees and signed a consent order saying they would not make such a claim anymore, based on the evidence at that time. In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up. A slew of other adverse events such as lacrimation, nasal congestion, mucocutaneous lesions, glycosuria, hypotension, and ECG abnormalities (DISEASE OF THE HEART AND LUNGS) have also been reported as well as allergic reactions (Wax, 2013) to EDTA. Prolonged treatment with calcium EDTA gives rise to depletion of magnesium and trace-metal depletion, the most marked being due to the excretion of zinc. Zinc depletion destroys your cells’ ability to absorb nutrients and leads to diabetes. A 2015 study entitled, Quality of Life Outcomes with a Disodium EDTA Chelation Regimen for Coronary Disease: Results from the TACT Randomized Trial concluded with this statement: “In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up.” Severe kidney damage from EDTA chelation therapy was reported in a (Nissel 1986) trial. In a very short period of time, EDTA causes kidneys to shut down in complete failure. A study from 2015 suggests EDTA chelation for myocardial infarction with “modest” benefits to cardio health. However, I would suggest that the moderate benefits of this study were due to the high doses of vitamin C administered. A 2017 study on EDTA chelation for atherosclerosis and Miocardial Infraction concluded: “Unsubstantiated claims of chelation therapy as an effective treatment of atherosclerosis should be avoided and patients made aware of the inadequate evidence for efficacy and potential adverse effects, especially the harm that can occur if used as a substitute for proven therapies.” In a 2018 EDTA trial it was concluded: “These results… are not sufficient to support the routine use of chelation therapy for treatment of patients who have had an MI (Miocardial Infraction)”. A study from 2023 entitled, Chelation Therapy Associated with Antioxidant Supplementation Can Decrease Oxidative Stress and Inflammation in Multiple Sclerosis: Preliminary Results proved a flop with two participants discontinuing their trial participation. EDTA for lead poisoning DEBUNKED EDTA has also been touted as a treatment for lead poisoning. Because of its adverse effects, calcium EDTA was replaced by DMSA in the treatment of lead poisoning (Aposhian et al., 1995) in 1995. CaEDTA has also been used for the treatment of cases with manganese toxicity, but the result was neurotoxic symptoms resembling PARKINSONISM (Andersen, 1999). A 2004 trial showed that EDTA actually REDISTRIBUTES LEAD TO THE BRAIN after acute or chronic lead exposure (Andersen, 2004). Another trial proved adverse effects in 5 patients receiving EDTA at an outpatient chelation clinic in 2002, and all patients experienced gastrointestinal and musculoskeletal symptoms. Oral exposure to EDTA (2002) had produced adverse reproductive and developmental effects in animals. EDTA did not make it past the animal or human trials, so why are medical doctors using it in humans? A 2002 EDTA trial was performed on humans as a test for “chelation” therapy by a chelation clinic, demonstrating adverse events in 5 out of 5 patients. Additionally, EDTA is a persistent organic pollutant (POP). In that case, each intake would only be partially excreted, while the remaining chemicals build up in the body and produce cell death. And long-term exposure to calcium disodium EDTA creates toxicity and kidney damage. EDTA Snakeoil Salesmen In March 2023, Ana Maria Mihalcea interviewed Dr. Michael Roth who claims that EDTA is a “synthetic amino acid related to vinegar.” Together they make a slew of medical claims that are not scientifically proven, such as that EDTA “detoxifies covid vaccine, heavy metals, graphene oxide, parasites, hydrogels, and nanoparticles”. The only scientific tool Ana Maria uses to back her claims is dark field microscopy. You cannot see nanoparticles with a dark field microscope. It takes a spectroscopy microscope to identify nanoparticles. Her medical claims are simply fabricated and unscientific lies. Ana Maria and Dr. Ross made additional unproven medical statements that “EDTA removes the effects of a heart attack, can bring back the elderly from senility and Alzheimer’s, reduces blood pressure, detoxifies several snake and spider venoms, lowers insulin, smooths skin and wrinkles, ” and a host of other laughable health claims that aren’t backed by anything. Incidentally, Dr. Ross is now dead. “Dr. Roth sadly passed away on March 11/2023” My sources informed me that Dr. Rashid Buttar was using EDTA. Given that he was already severely poisoned as Stew Peter’s reported, using EDTA Acid would have been enough to tip him over the edge and kill him. EDTA is not an approved pharmaceutical drug. It was Covid Emergency approved by the FDA under an Emergency Use Authorization (EUA), just like the modified RNA (modRNA) Covid-19 vaccine nanotechnology. The National Center for Complementary and Integrative Health (.gov) makes it clear that the use of EDTA chelation for heart disease has not been approved by the FDA. Ana Maria has been touting EDTA as an “antioxidant” when it is not. She even published to her Substack that EDTA is an “Antioxidant” when in fact it’s an acid poison and an oxidant. Many people saw it on her Substack before she removed it. I’ve had over a dozen clients come to me extremely sick from EDTA pills and EDTA IV infusion. Some told me they thought it was a natural substance due to Ana Maria’s false advertising and medical malfeasance. A Medical Doctor is licensed to know wether EDTA Acid is an oxidant poison or an antioxidant. Not knowing this and inducing the death of a patient is not an acceptable excuse. Ana Maria is criminally liable. EDTA is an oxidant when used internally. The studies that refer to EDTA as an “antioxidant” are in vitro lab studies, not in vivo (inside the body). EDTA is used to preserve cell specimens for chemistry lab work because it prevents blood coagulation and oxidation of cells in a petri dish where it’s used for diagnostic purposes. This is the kind of “antioxidant” the studies are referring to. But when you infuse EDTA Acid into the human body, it acts as an oxidant poison. EDTA also will not decoagulate the blood in vivo (inside the body). But I can see how people who cannot read peer-reviewed literature could be deceived and manipulated by snake oil salesmen. For example, a study entitled, “Comparative study of the antioxidant capability of EDTA and Irganox”. EDTA is a preservative used in laboratories to preserve cells for scientific lab research. EDTA prevents the oxidation of cells in a petri dish. Oxygen causes cells to deteriorate, but labs need them to last longer for research purposes. When used inside the human body (in vivo), it’s a different story. Then EDTA acts as an oxidant poison, not an antioxidant. So this has a very different meaning. One of the well documented and widely known adverse events from EDTA “chelation” is DEATH, according to Mount Sinai. Other serious side effects that have been reported include low blood sugar, diminished calcium levels, headache, nausea, dangerously low blood pressure, kidney failure, organ damage, irregular heartbeat, seizures, or even death. I have to wonder if Ana Maria Mihalcea is informing her patients that death is a potential adverse event to EDTA chelation? In a March 24, 2024, broadcast that Ana Maria released, at the 53:24 minute mark, she makes a chilling confession: “I already have had… uh… patients die from the shedding” How many of Ana Maria Mihalcea’s patients have been killed by her EDTA infusion protocol? I was horrified when I heard Ana Maria’s confession because I haven’t had any clients die from shedding! I’ve treated many people who were extremely sick from shedding, and I helped them all to detox effectively. Some clients came to me after several hospitalizations from extreme shedding but none of them died in my care! Nobody needs to die from shedding if they use an effective detox protocol. Between 1-2 years, Ana Maria has been claiming that EDTA detoxes graphene, dissolves graphene and chelates heavy metals, but experts such as Dr. Robert Young and Dr. Judy Mikovitz told me this is impossible. Ana Maria has gone so far as to produce a medical study with unscientific claims right in the title, “EDTA Chelation Dissolves the Artificial Intelligence Magnetic Hydrogel Weapon”. The study was also promoted by Health Canada. In her study, Ana Maria claims that EDTA can “detoxify the body even from Graphene”. EDTA is not a detox agent! Again, it’s an oxidant that degrades cells whereas genuine antioxidants repair cells. Ana Maria does in fact know about oxidant poisons. In an interview from December 2022, she referred to graphene as an oxidant. At least she’s correct about something. Saul Green, Ph.D., and Wallace I. Sampson, M.D. wrote in great detail about the Implausibility of EDTA Chelation Therapy, stating: “EDTA chelation effectiveness is implausible; (2) the preponderance of evidence shows ineffectiveness; and (3) EDTA augments oxidative reactions involving iron instead of inhibiting them, resulting in increased likelihood of production of oxygen free radicals rather than neutralization of them, as claimed.” EDTA a precurser to cellular transfection The Rockefeller Institue of Medicine has done clinical research on EDTA. One particular study entitled, Studies of Cell Deformity from 1967, shows that cells will degrade from EDTA exposure, which also induces “deformation” on their surfaces. The trial demonstrated that EDTA stops cellular synthesis of calcium. They learned that calcium is bound to anionic sites at the cell periphery, some of which are located at the cellular electrokinetic surface. Due to Rockefeller’s research, EDTA is now used in electrophoresis which is a laboratory technique used to separate DNA, RNA or protein molecules based on their size and electrical charge. An electric current is used to move the molecules through a gel or other matrix, according to the National Human Genome Research Institute. In agarose gel electrophoresis, EDTA is added for chelating the magnesium ions which are cofactors for DNA nucleases. Hence, activity of DNA nucleases that may be present is inhibited, and “DNA is protected from degrading”. This is why EDTA is an effective transfection agent because it dissolves parts of your DNA, preserving cells for lab research in vitro. Gel electrophoresis using EDTA is routinely used for detection and size analysis of proteins and nucleic acid. DMSO is used with EDTA in this process. This destruction of cells makes transfection (gene editing) of cells easier using CRISPR-Cas9 which splices and dices the genome in vivo, as this study explains entitled, “Inhibition of CRISPR-Cas9 ribonucleoprotein complex assembly by anti-CRISPR AcrIIC2”. EDTA was found to be genotoxic in laboratory animals. A study from 1983 demonstrates that EDTA induces gene mutations and chromosomal breakage, meaning that genetic mutations will be passed on your offspring, affecting generations to come, according to this Genetic Toxicology of EDTA study from 1983. Calcium chelate of EDTA (CaEDTA) “chelation” has shown teratogenic effects (Catsch & Harmuth-Hoene, 1976), which are central nervous system depression and peripheral neuropathy. EDTA produced abnormalities in pups of rats removed by cesarian section on day 21 of the study. Increases in several abnormalities (cleft palate, adactyly or syndactyly, abnormal rib or abnormal vertebrae) were observed with increased doses of CaEDTA. EDTA improves transfection of embryonic stem cells lines (hESC) in cells, according to the NIH. According to a peer reviewed paper from the NIH, EDTA is a precursor to cellular transfection. “We found that chemically abrading the differentiated CACO-2 human intestinal epithelial cell layer by a trypsin and EDTA pretreatment (before the use of detergent-like transfection reagents) dramatically improved transfection efficiency in this polar, differentiated model. Although this treatment did improve the transfection efficiency, it also induced leakiness in the epithelial barrier by both opening tight junctional complexes and by creating holes in the cell layer because of low-level cell death and detachment. Thus, this approach to enhance the transfection efficiency of polar, differentiated cells will be useful for assessment of the effect of the transfected/expressed protein on (re)formation of an epithelial barrier..." Thermo Fisher Scientific Inc. Fetal Bovine Serum for human transfection also uses EDTA. An NIH study entitled, “Kinetic Basis for DNA Target Specificity of CRISPR-Cas12a” reveals that EDTA enables rapid binding to DNA during gene editing (transfection). Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” explains: “CAS12a is an RNA-guided, programmable genome editing enzyme found within bacterial adaptive immune pathways. Unlike CRISPR-Cas9, Cas12a uses only a single catalytic site to both cleave target double-stranded DNA (dsDNA) (cis-activity) and indiscriminately degrade single-stranded DNA (ssDNA) (trans-activity).” According to the study, “A DNA loading buffer of 45% formamide and 15 mM EDTA, with a trace amount of xylene cyanol and bromophenol blue…” is used to transfect the human genome. So, EDTA is a transfection agent used with CRISPR-Cas9 to edit the human genome. Does EDTA actually dissolve graphene, as Ana Maria claims? The answer is NO! EDTA oxidant is used to reduce graphene to Reduced Graphene Oxide (RGO) form. Graphene is reduced by oxidation. Rather than dissolving graphene, EDTA reduces it to Graphene Oxide Nanoparticles otherwise known as Quantum Dots. Graphene oxide is more toxic than graphene, as I documented in my article entitled, “Graphene Oxide The Vector For Covid-19 Democide”. I will emphasize again that Graphene Oxide Quantum Dots cannot be seen with a dark field microscope. So Ana Maria’s claims that EDTA is detoxing graphene from the human body is unscientific. EDTA chelation for graphene nanocomposites EDTA chelation is NOT effective in removing metals from the human body. It's actually a different kind of chelation that’s used to create electrochemical sensors (biosensors) when combined with GRAPHENE! EDTA serves as a connecting mediator between NiHCF (Graphene Oxide Nanoparticles and Nickle) and graphene nanosheets. EDTA is used with metal nanoparticles, metal oxides, graphene, carbon nanotubes, and quantum dots to stabilize the technology for a more uniform distribution throughout the body. A Science Direct paper entitled, “Highly sensitive ascorbid acid sensors from EDTA chelation derived nickel hexacyanoferrate/graphene nanocomposites” reveals that EDTA is used to create Graphene/Nickel, AA sensor nanocomposites. “EDTA chelation stragey” is used for the “homogeneously distrubuted" NiHCF” (Nickel hexacyanoferrate composite) on graphene sheets. EDTA residue-supported pyramidal and spherical nanoparticles of NiHCF deposited on graphene sheets is used to create biosensors for the formation of Graphene/Nickel hydrogels. The graphene hydrogel nanocomposite sensors (Gr/NiHCF) are used as externally controlled biosensing tools. They tell us it’s used to test for ascorbic acid, but the application of this technology is for “human life” as well as for industrial use. See link here. Graphene oxide/Lauric acid nanoparticles are modified using EDTA. Lauric acid nanoparticles is suggested as a “prospective drug carrier” for oral nanoparticle-mediated sustained drug delivery (timed release technology) used for the removal of Pb(II) ions (lead). However, studies show there are cytotoxic results. Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” demonstrates how EDTA improves transfection and modification of the human genome. Once Graphene is reduced to Graphene Oxide, due to its small particulate size, you can no longer identify it using a Dark Field Microscope. Ana Maria is using a dark field scope, not a spectroscopy microscope, which is the only instrument that can measure GON and Quantum Dots. So what is Ana Maria doing with EDTA infusions? She’s creating a metal-EDTA complex that stabilizes and strengthens the graphene-based nanotech weapon system and enables it to spread more readily throughout the body, for human transfection. She uses “light and sound healing techniques” to activate the delayed release technology before administering EDTA infusion, as she reveals in an interview here. EDTA is a poison acid that dissolves DNA. It's used to prime the cells’ DNA for transfection. EDTA disrupts the surface of skin cells so that other chemicals can penetrate more easily and CRISPR-Cas9 gene editing technology can work more efficiently. The NIH describes EDTA’s enhanced cellular transfection: “Flow cytometric analysis using an enhanced green fluorescent protein vector showed a significantly increased transfection efficiency of EDTA method compared to standard enzyme method. In addition, the EDTA approach maintained stable cell viability and recovery rate of hESCs after transfection.” Another study published in Research Gate, confirms that EDTA increases cellular transfection, along with using chloroquine. Graphene Oxide Quantum Dots (GOQD-HA) nanocomposite use EDTA for tissue-specific delivery of Metformin, an anti-diabetic drug otherwise known as insulin. Conclusion Beware of snakeoil salesmen! Never trust pharmaceuticals! Superior heavy metal chelation supplements exist such as ASEA redox molecules and Master Peace, sign up and order here. Medicines made from nature are always superior to pharmaceutical drugs. Finally, be sure your Naturopathic Doctor is competent! Schedule a health consultation with me for a customized detox protocol and complete cellular health restoration. https://substack.com/home/post/p-144979143
    SUBSTACK.COM
    EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed
    “I already have had.. uh.. patients die from shedding” - Ana Maria Mihalcea, M.D.
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  • Unlock Your Brain's Hidden Genius with a Simple Daily Ritual

    Have you ever wondered why some people just seem to be naturally blessed with intelligence, happiness, and luck? It's not because of "better genetics" but because they've activated their Genius Wave.

    What is the Genius Wave?

    It's a powerful brainwave, about the size of a cashew, over 200 million years old, but currently dormant in most of us. This brainwave, once activated, is linked to extraordinary abilities:

    Great ideas just come to you.
    You learn faster.
    Lucky things happen.

    NASA-Backed Research

    Dr. James Rivers, a key contributor to NASA’s Neuroscience Program and a Stanford-trained researcher, discovered a 7-second ritual that can activate this Genius Wave. This method is backed by research from major universities like Stanford and Yale, proving its effectiveness by connecting several regions of your brain together simultaneously.

    Real-Life Transformations

    Thousands of people have experienced life-changing results:

    One grandmother, struggling with memory loss, showed almost immediate signs of enhanced cognitive health and memory after listening to a 7-minute song.

    A father whose son was failing in school let him listen to this soundwave every morning. The boy’s grades skyrocketed from C’s and D’s to straight A’s before midterms.

    Another person reportedly attracted the love of her life just a week after starting the ritual, despite being divorced and single for three years.

    The Secret Revealed

    This revelation was so profound that elite circles, including the CIA, whispered about the potential of pineal gland activation for extraordinary manifestations. Dr. Rivers' safe, proven 7-Second Brain Trick is now available to everyone.
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    How to Activate Your Genius Wave

    The best part? You don’t need to meditate, visualize, or manifest. Just pop on some headphones and listen to this specially designed 7-minute song every morning. Transform yourself into a walking good luck charm.

    Join the thousands of Americans who have already changed their lives with this incredible discovery. Tap the button below to learn more and start your transformation today.
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    #UnlockYourGenius #BrainPower #DailyRitual #ActivateYourMind #GeniusWave #BrainBoost #HiddenPotential #UnlockYourBrain #MentalMastery #DailyMindHack #BoostYourBrain #IntelligenceUnlocked #LearnFaster #LuckyLife #BrainwaveActivation #GeniusMindset #UnlockSuccess #BrainHacks #MindOverMatter #GeniusUnlock
    Unlock Your Brain's Hidden Genius with a Simple Daily Ritual Have you ever wondered why some people just seem to be naturally blessed with intelligence, happiness, and luck? It's not because of "better genetics" but because they've activated their Genius Wave. What is the Genius Wave? It's a powerful brainwave, about the size of a cashew, over 200 million years old, but currently dormant in most of us. This brainwave, once activated, is linked to extraordinary abilities: 💡 Great ideas just come to you. 💡 You learn faster. 💡 Lucky things happen. NASA-Backed Research Dr. James Rivers, a key contributor to NASA’s Neuroscience Program and a Stanford-trained researcher, discovered a 7-second ritual that can activate this Genius Wave. This method is backed by research from major universities like Stanford and Yale, proving its effectiveness by connecting several regions of your brain together simultaneously. Real-Life Transformations Thousands of people have experienced life-changing results: 🔮 One grandmother, struggling with memory loss, showed almost immediate signs of enhanced cognitive health and memory after listening to a 7-minute song. 🔮 A father whose son was failing in school let him listen to this soundwave every morning. The boy’s grades skyrocketed from C’s and D’s to straight A’s before midterms. 🔮 Another person reportedly attracted the love of her life just a week after starting the ritual, despite being divorced and single for three years. The Secret Revealed This revelation was so profound that elite circles, including the CIA, whispered about the potential of pineal gland activation for extraordinary manifestations. Dr. Rivers' safe, proven 7-Second Brain Trick is now available to everyone. Click Here Now 👉 https://bit.ly/TheGeniusWave2 How to Activate Your Genius Wave The best part? You don’t need to meditate, visualize, or manifest. Just pop on some headphones and listen to this specially designed 7-minute song every morning. Transform yourself into a walking good luck charm. Join the thousands of Americans who have already changed their lives with this incredible discovery. Tap the button below to learn more and start your transformation today. Click Here Now 👉 https://bit.ly/TheGeniusWave2 #UnlockYourGenius #BrainPower #DailyRitual #ActivateYourMind #GeniusWave #BrainBoost #HiddenPotential #UnlockYourBrain #MentalMastery #DailyMindHack #BoostYourBrain #IntelligenceUnlocked #LearnFaster #LuckyLife #BrainwaveActivation #GeniusMindset #UnlockSuccess #BrainHacks #MindOverMatter #GeniusUnlock
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  • Air Vax — The Latest mRNA Delivered Into Lungs
    (Mercola)—Yale University researchers have developed a new airborne method for delivering mRNA right to your lungs. The team has also used the method to vaccinate mice intranasally,1 opening the door for human testing in the near future.

    While scientists are hailing the creation as an easy way to vaccinate the masses, critics wonder if the development of an airborne vaccine could be used for nefarious purposes, including covert bioenhancements,2 which have already been recommended in academic literature.3

    Yale Team Develops Airborne mRNA, Delivers It to Lungs

    In a study on mice, Yale scientists created polymer nanoparticles to encapsulate mRNA, making it inhalable so it can reach the lungs. Courtney Malo, editor with Science Translational Medicine, which published the study, explained:4

    “The ability to efficiently deliver mRNA to the lung would have applications for vaccine development, gene therapy, and more. Here, Suberi et al. showed that such mRNA delivery can be accomplished by encapsulating mRNAs of interest within optimized poly(amine-co-ester) polyplexes [nanoparticles].

    Polyplex-delivered mRNAs were efficiently translated into protein in the lungs of mice with limited evidence of toxicity. This platform was successfully applied as an intranasal SARS-CoV-2 vaccine, eliciting robust immune responses that conferred protection against subsequent viral challenge. These results highlight the potential of this delivery system for vaccine applications and beyond.”

    Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef

    MORE NEWS: Stephanopoulos Caught on Camera After Biden Interview: ‘I Don’t Think He Can Serve Four More Years’

    The team, led by cellular and molecular physiologist Mark Saltzman, explained that the inhalable mRNA vaccine successfully protected against SARS-CoV-2, which “opens the door to delivering other messenger RNA (mRNA) therapeutics for gene replacement therapy and other treatments in the lungs.”5

    For the study, mice received two intranasal doses of nanoparticles carrying mRNA COVID-19 vaccines, which proved to be effective in the animals. In the past, lung-targeted mRNA therapies had trouble making it into the cells necessary to express the encoded protein, known as poor transfection efficiency.6

    Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef

    “The Saltzman group got around this hurdle in part by using a nanoparticle made from poly(amine-co-ester) polyplexes, or PACE, a biocompatible and highly customizable polymer,” a Yale University news release explained.7 In a previous study, Saltzman had tried a “prime and spike” system to deliver COVID-19 shots, which involved injecting mRNA shots into a muscle, then spraying spike proteins into the nose.8

    It turned out the injection portion may be unnecessary, and Saltzman has high hopes for the airborne delivery method, beyond vaccines:9

    “In the new report, there is no intramuscular injection. We just gave two doses, a prime and a boost, intranasally, and we got a highly protective immune response. But we also showed that, generally, you can deliver different kinds of mRNA. So it’s not just good for a vaccine, but potentially also good for gene replacement therapy in diseases like cystic fibrosis and gene editing.

    We used a vaccine example to show that it works, but it opens the door to doing all these other kinds of interventions.”

    Air Vax Could ‘Radically Change’ How People Are Vaccinated

    MORE NEWS: Data Analyst Says Gold Will Be the “New Reserve Asset” — Time to Get the Gold Guide

    Saltzman says this “new method of delivery could ‘radically change the way people are vaccinated,’” making it easier to vaccinate people in remote areas or those who are afraid of needles.10 But that’s not all. An airborne vaccine makes it possible to rapidly disseminate it across a population.

    By releasing the vaccine in the air, there’s no need to inject each person individually — which is not only time-consuming but difficult if an individual objects to the shot. This isn’t the case with an airborne vaccine, which can be released into the air without consent or even the public’s knowledge.

    A similar strategy is being used with mRNA in shrimp, which are too small and numerous to be injected individually. Instead, an oral “nanovaccine” was created to stop the spread of a virus. Shai Ufaz, chief executive officer of ViAqua, which developed the technology, stated:11

    “Oral delivery is the holy grail of aquaculture health development due to both the impossibility of vaccinating individual shrimp and its ability to substantially bring down the operational costs of disease management while improving outcomes …”

    While the Yale scientists are targeting an intranasal mRNA product, the outcome is the same — get as many exposed as possible with the least amount of cost and effort. According to the Yale study:12

    “An inhalable platform for messenger RNA (mRNA) therapeutics would enable minimally invasive and lung-targeted delivery for a host of pulmonary diseases. Development of lung-targeted mRNA therapeutics has been limited by poor transfection efficiency and risk of vehicle-induced pathology.

    Here, we report an inhalable polymer-based vehicle for delivery of therapeutic mRNAs to the lung. We optimized biodegradable poly(amine-co-ester) (PACE) polyplexes [nanoparticles] for mRNA delivery using end-group modifications and polyethylene glycol. These polyplexes achieved high transfection of mRNA throughout the lung, particularly in epithelial and antigen-presenting cells.

    We applied this technology to develop a mucosal vaccine for severe acute respiratory syndrome coronavirus 2 and found that intranasal vaccination with spike protein–encoding mRNA polyplexes induced potent cellular and humoral adaptive immunity and protected susceptible mice from lethal viral challenge. Together, these results demonstrate the translational potential of PACE polyplexes for therapeutic delivery of mRNA to the lungs.”

    US Government Has History of Bioweapons Release

    When you put the pieces of the puzzle together, a disturbing picture emerges. As reported by The Epoch Times, we have a history of the U.S. government taking extreme measures to mandate and promote COVID-19 shots to the public. Now, researchers have developed an airborne mRNA vaccine, offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent.13

    Is there proof that the government or another entity has plans to covertly release an air vax on the population? No. But there is a history of it carrying out secret bioweapon simulations on Americans. In 1950, the U.S. Navy sprayed Serratia marcescens bacteria into the air near San Francisco over a period of six days.

    MORE NEWS: Washington State Is ‘Ground Zero’ for EV Charging Port Thefts

    Dubbed “Operation Sea Spray,” the project was intended to determine how susceptible the city was to a bioweapon attack. Serratia marcescens turns whatever it touches bright red, making it easy to track. It spread throughout the city, as residents inhaled the microbes from the air. While the U.S. military initially thought Serratia marcescens wouldn’t harm humans, an outbreak occurred, with some developing urinary tract infections as a result.

    At least one person died “and some have suggested that the release forever changed the area’s microbial ecology,” Smithsonian Magazine reported.14 This wasn’t an isolated incident, as the U.S. government carried out many other experiments across the U.S. over the next 20 years.15 So, while it’s disturbing to think of an air vax experiment being conducted on an unsuspecting public, it’s not unprecedented.

    Bioethics Study Promotes Covert, Compulsory Bioenhancement

    Adding to the story is academic endorsement of the use of compulsory, covert bioenhancements. Writing in the journal Bioethics,16 Parker Crutchfield with Western Michigan University, Homer Stryker M.D. School of Medicine, discusses moral bioenhancements, which refers to the use of biomedical means to trigger moral improvements.

    Drug treatments, including vaccines, and genetic engineering are potential examples of bioenhancements.17 Further, according to Crutchfield:18

    “It is necessary to morally bioenhance the population in order to prevent ultimate harm. Moral bioenhancement is the potential practice of influencing a person’s moral behavior by way of biological intervention upon their moral attitudes, motivations, or dispositions.

    The technology that may permit moral bioenhancement is on the scale between nonexistent and nascent, but common examples of potential interventions include infusing water supplies with pharmaceuticals that enhance empathy or altruism or otherwise intervening on a person’s emotions or motivations, in an attempt to influence the person’s moral behavior.”

    Some argue that moral bioenhancements should be compulsory for the greater good. Crutchfield believes this doesn’t go far enough. He also wants them to be covert:19

    “I take this argument one step further, arguing that if moral bioenhancement ought to be compulsory, then its administration ought to be covert rather than overt. This is to say that it is morally preferable for compulsory moral bioenhancement to be administered without the recipients knowing that they are receiving the enhancement.”

    MORE NEWS: Suspect Arrested After Shooting Houston Police Officer Amid Hurricane Recovery

    He even goes so far as to suggest “a covert compulsory program promotes values such as liberty, utility, equality and autonomy better than an overt program does.”20 So here we have evidence of academic support for covertly releasing drugs and other bioenhancements onto the public. This, combined with the creation of an airborne mRNA vaccine and the government’s history of experimenting on the public, paints an unsettling picture of the future.

    Problems With mRNA COVID Shots Persist

    Aside from the concerns of airborne delivery, mRNA COVID-19 shots are associated with significant risks — no matter how you’re exposed. People ages 65 and older who received Pfizer’s updated (bivalent) COVID-19 booster shot may be at increased risk of stroke, according to an announcement made by the U.S. Centers for Disease Control and Prevention and the Food and Drug Administration.21

    Further, a large study from Israel22 revealed that Pfizer’s COVID-19 mRNA jab is associated with a threefold increased risk of myocarditis,23 leading to the condition at a rate of 1 to 5 events per 100,000 persons.24 Other elevated risks were also identified following the COVID jab, including lymphadenopathy (swollen lymph nodes), appendicitis and herpes zoster infection.25

    At least 16,183 people also say they’ve developed tinnitus after receiving a COVID-19 shot.26 The reports were filed with the CDC’s Vaccine Adverse Event Reporting System (VAERS) database. But considering only between 1%27 and 10%28 of adverse reactions are ever reported to VAERS, the actual number is likely much higher.

    It’s because of risks like these that informed consent is essential for any medical procedure, including vaccinations. The development of airborne mRNA jabs, however, makes the possibility of informed consent being taken away all the more real.

    1, 4 Science Translational Medicine August 16, 2023, Vol 15, Issue 709
    2, 13 The Epoch Times September 5, 2023
    3 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29
    5, 6, 7, 8, 9 Yale School of Engineering & Applied Science, News & Events August 16, 2023
    10 Bitchute, Truther’s Lair September 5, 2023, 5:09
    11 Fish Farmer September 5, 2023
    12 Science Translational Medicine August 16, 2023, Vol 15, Issue 709, Abstract
    14, 15 Smithsonian Magazine July 6, 2015
    16, 18 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29., Intro
    17 Topoi volume 38, pages 1–5 (2019)
    19, 20 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29., Abstract
    21 U.S. FDA January 13, 2023
    22, 24, 25 The New England Journal of Medicine August 25, 2021
    23 MedPage Today August 25, 2021
    26 NBC News April 23, 2023
    27 Harvard Pilgrim Health Care report submitted to the U.S. Department of Health and Human Services, 2011, Page 6
    28 BMJ 2005;330:433
    Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef



    It’s becoming increasingly clear that fiat currencies across the globe, including the U.S. Dollar, are under attack. Paper money is losing its value, translating into insane inflation and less value in our life’s savings.

    Genesis Gold Group believes physical precious metals are an amazing option for those seeking to move their wealth or retirement to higher ground. Whether Central Bank Digital Currencies replace current fiat currencies or not, precious metals are poised to retain or even increase in value. This is why central banks and mega-asset managers like BlackRock are moving much of their holdings to precious metals.

    As a Christian company, Genesis Gold Group has maintained a perfect 5 out of 5 rating with the Better Business Bureau. Their faith-driven values allow them to help Americans protect their life’s savings without the gimmicks used by most precious metals companies. Reach out to them today to see how they can streamline the rollover or transfer of your current and previous retirement accounts.

    https://discernreport.com/air-vax-the-latest-mrna-delivered-into-lungs/
    Air Vax — The Latest mRNA Delivered Into Lungs (Mercola)—Yale University researchers have developed a new airborne method for delivering mRNA right to your lungs. The team has also used the method to vaccinate mice intranasally,1 opening the door for human testing in the near future. While scientists are hailing the creation as an easy way to vaccinate the masses, critics wonder if the development of an airborne vaccine could be used for nefarious purposes, including covert bioenhancements,2 which have already been recommended in academic literature.3 Yale Team Develops Airborne mRNA, Delivers It to Lungs In a study on mice, Yale scientists created polymer nanoparticles to encapsulate mRNA, making it inhalable so it can reach the lungs. Courtney Malo, editor with Science Translational Medicine, which published the study, explained:4 “The ability to efficiently deliver mRNA to the lung would have applications for vaccine development, gene therapy, and more. Here, Suberi et al. showed that such mRNA delivery can be accomplished by encapsulating mRNAs of interest within optimized poly(amine-co-ester) polyplexes [nanoparticles]. Polyplex-delivered mRNAs were efficiently translated into protein in the lungs of mice with limited evidence of toxicity. This platform was successfully applied as an intranasal SARS-CoV-2 vaccine, eliciting robust immune responses that conferred protection against subsequent viral challenge. These results highlight the potential of this delivery system for vaccine applications and beyond.” Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef MORE NEWS: Stephanopoulos Caught on Camera After Biden Interview: ‘I Don’t Think He Can Serve Four More Years’ The team, led by cellular and molecular physiologist Mark Saltzman, explained that the inhalable mRNA vaccine successfully protected against SARS-CoV-2, which “opens the door to delivering other messenger RNA (mRNA) therapeutics for gene replacement therapy and other treatments in the lungs.”5 For the study, mice received two intranasal doses of nanoparticles carrying mRNA COVID-19 vaccines, which proved to be effective in the animals. In the past, lung-targeted mRNA therapies had trouble making it into the cells necessary to express the encoded protein, known as poor transfection efficiency.6 Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef “The Saltzman group got around this hurdle in part by using a nanoparticle made from poly(amine-co-ester) polyplexes, or PACE, a biocompatible and highly customizable polymer,” a Yale University news release explained.7 In a previous study, Saltzman had tried a “prime and spike” system to deliver COVID-19 shots, which involved injecting mRNA shots into a muscle, then spraying spike proteins into the nose.8 It turned out the injection portion may be unnecessary, and Saltzman has high hopes for the airborne delivery method, beyond vaccines:9 “In the new report, there is no intramuscular injection. We just gave two doses, a prime and a boost, intranasally, and we got a highly protective immune response. But we also showed that, generally, you can deliver different kinds of mRNA. So it’s not just good for a vaccine, but potentially also good for gene replacement therapy in diseases like cystic fibrosis and gene editing. We used a vaccine example to show that it works, but it opens the door to doing all these other kinds of interventions.” Air Vax Could ‘Radically Change’ How People Are Vaccinated MORE NEWS: Data Analyst Says Gold Will Be the “New Reserve Asset” — Time to Get the Gold Guide Saltzman says this “new method of delivery could ‘radically change the way people are vaccinated,’” making it easier to vaccinate people in remote areas or those who are afraid of needles.10 But that’s not all. An airborne vaccine makes it possible to rapidly disseminate it across a population. By releasing the vaccine in the air, there’s no need to inject each person individually — which is not only time-consuming but difficult if an individual objects to the shot. This isn’t the case with an airborne vaccine, which can be released into the air without consent or even the public’s knowledge. A similar strategy is being used with mRNA in shrimp, which are too small and numerous to be injected individually. Instead, an oral “nanovaccine” was created to stop the spread of a virus. Shai Ufaz, chief executive officer of ViAqua, which developed the technology, stated:11 “Oral delivery is the holy grail of aquaculture health development due to both the impossibility of vaccinating individual shrimp and its ability to substantially bring down the operational costs of disease management while improving outcomes …” While the Yale scientists are targeting an intranasal mRNA product, the outcome is the same — get as many exposed as possible with the least amount of cost and effort. According to the Yale study:12 “An inhalable platform for messenger RNA (mRNA) therapeutics would enable minimally invasive and lung-targeted delivery for a host of pulmonary diseases. Development of lung-targeted mRNA therapeutics has been limited by poor transfection efficiency and risk of vehicle-induced pathology. Here, we report an inhalable polymer-based vehicle for delivery of therapeutic mRNAs to the lung. We optimized biodegradable poly(amine-co-ester) (PACE) polyplexes [nanoparticles] for mRNA delivery using end-group modifications and polyethylene glycol. These polyplexes achieved high transfection of mRNA throughout the lung, particularly in epithelial and antigen-presenting cells. We applied this technology to develop a mucosal vaccine for severe acute respiratory syndrome coronavirus 2 and found that intranasal vaccination with spike protein–encoding mRNA polyplexes induced potent cellular and humoral adaptive immunity and protected susceptible mice from lethal viral challenge. Together, these results demonstrate the translational potential of PACE polyplexes for therapeutic delivery of mRNA to the lungs.” US Government Has History of Bioweapons Release When you put the pieces of the puzzle together, a disturbing picture emerges. As reported by The Epoch Times, we have a history of the U.S. government taking extreme measures to mandate and promote COVID-19 shots to the public. Now, researchers have developed an airborne mRNA vaccine, offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent.13 Is there proof that the government or another entity has plans to covertly release an air vax on the population? No. But there is a history of it carrying out secret bioweapon simulations on Americans. In 1950, the U.S. Navy sprayed Serratia marcescens bacteria into the air near San Francisco over a period of six days. MORE NEWS: Washington State Is ‘Ground Zero’ for EV Charging Port Thefts Dubbed “Operation Sea Spray,” the project was intended to determine how susceptible the city was to a bioweapon attack. Serratia marcescens turns whatever it touches bright red, making it easy to track. It spread throughout the city, as residents inhaled the microbes from the air. While the U.S. military initially thought Serratia marcescens wouldn’t harm humans, an outbreak occurred, with some developing urinary tract infections as a result. At least one person died “and some have suggested that the release forever changed the area’s microbial ecology,” Smithsonian Magazine reported.14 This wasn’t an isolated incident, as the U.S. government carried out many other experiments across the U.S. over the next 20 years.15 So, while it’s disturbing to think of an air vax experiment being conducted on an unsuspecting public, it’s not unprecedented. Bioethics Study Promotes Covert, Compulsory Bioenhancement Adding to the story is academic endorsement of the use of compulsory, covert bioenhancements. Writing in the journal Bioethics,16 Parker Crutchfield with Western Michigan University, Homer Stryker M.D. School of Medicine, discusses moral bioenhancements, which refers to the use of biomedical means to trigger moral improvements. Drug treatments, including vaccines, and genetic engineering are potential examples of bioenhancements.17 Further, according to Crutchfield:18 “It is necessary to morally bioenhance the population in order to prevent ultimate harm. Moral bioenhancement is the potential practice of influencing a person’s moral behavior by way of biological intervention upon their moral attitudes, motivations, or dispositions. The technology that may permit moral bioenhancement is on the scale between nonexistent and nascent, but common examples of potential interventions include infusing water supplies with pharmaceuticals that enhance empathy or altruism or otherwise intervening on a person’s emotions or motivations, in an attempt to influence the person’s moral behavior.” Some argue that moral bioenhancements should be compulsory for the greater good. Crutchfield believes this doesn’t go far enough. He also wants them to be covert:19 “I take this argument one step further, arguing that if moral bioenhancement ought to be compulsory, then its administration ought to be covert rather than overt. This is to say that it is morally preferable for compulsory moral bioenhancement to be administered without the recipients knowing that they are receiving the enhancement.” MORE NEWS: Suspect Arrested After Shooting Houston Police Officer Amid Hurricane Recovery He even goes so far as to suggest “a covert compulsory program promotes values such as liberty, utility, equality and autonomy better than an overt program does.”20 So here we have evidence of academic support for covertly releasing drugs and other bioenhancements onto the public. This, combined with the creation of an airborne mRNA vaccine and the government’s history of experimenting on the public, paints an unsettling picture of the future. Problems With mRNA COVID Shots Persist Aside from the concerns of airborne delivery, mRNA COVID-19 shots are associated with significant risks — no matter how you’re exposed. People ages 65 and older who received Pfizer’s updated (bivalent) COVID-19 booster shot may be at increased risk of stroke, according to an announcement made by the U.S. Centers for Disease Control and Prevention and the Food and Drug Administration.21 Further, a large study from Israel22 revealed that Pfizer’s COVID-19 mRNA jab is associated with a threefold increased risk of myocarditis,23 leading to the condition at a rate of 1 to 5 events per 100,000 persons.24 Other elevated risks were also identified following the COVID jab, including lymphadenopathy (swollen lymph nodes), appendicitis and herpes zoster infection.25 At least 16,183 people also say they’ve developed tinnitus after receiving a COVID-19 shot.26 The reports were filed with the CDC’s Vaccine Adverse Event Reporting System (VAERS) database. But considering only between 1%27 and 10%28 of adverse reactions are ever reported to VAERS, the actual number is likely much higher. It’s because of risks like these that informed consent is essential for any medical procedure, including vaccinations. The development of airborne mRNA jabs, however, makes the possibility of informed consent being taken away all the more real. 1, 4 Science Translational Medicine August 16, 2023, Vol 15, Issue 709 2, 13 The Epoch Times September 5, 2023 3 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29 5, 6, 7, 8, 9 Yale School of Engineering & Applied Science, News & Events August 16, 2023 10 Bitchute, Truther’s Lair September 5, 2023, 5:09 11 Fish Farmer September 5, 2023 12 Science Translational Medicine August 16, 2023, Vol 15, Issue 709, Abstract 14, 15 Smithsonian Magazine July 6, 2015 16, 18 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29., Intro 17 Topoi volume 38, pages 1–5 (2019) 19, 20 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29., Abstract 21 U.S. FDA January 13, 2023 22, 24, 25 The New England Journal of Medicine August 25, 2021 23 MedPage Today August 25, 2021 26 NBC News April 23, 2023 27 Harvard Pilgrim Health Care report submitted to the U.S. Department of Health and Human Services, 2011, Page 6 28 BMJ 2005;330:433 Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef It’s becoming increasingly clear that fiat currencies across the globe, including the U.S. Dollar, are under attack. Paper money is losing its value, translating into insane inflation and less value in our life’s savings. Genesis Gold Group believes physical precious metals are an amazing option for those seeking to move their wealth or retirement to higher ground. Whether Central Bank Digital Currencies replace current fiat currencies or not, precious metals are poised to retain or even increase in value. This is why central banks and mega-asset managers like BlackRock are moving much of their holdings to precious metals. As a Christian company, Genesis Gold Group has maintained a perfect 5 out of 5 rating with the Better Business Bureau. Their faith-driven values allow them to help Americans protect their life’s savings without the gimmicks used by most precious metals companies. Reach out to them today to see how they can streamline the rollover or transfer of your current and previous retirement accounts. https://discernreport.com/air-vax-the-latest-mrna-delivered-into-lungs/
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  • mRNA COVID jabs found to spread from vaccinated to unvaccinated via AEROSOLS

    New peer-reviewed research published in the journal ImmunoHorizons shows that individuals who have been "vaccinated" for the Wuhan coronavirus (COVID-19) can spread antibodies generated by the injections to unvaccinated individuals through aerosols.
    Because of the lengthy mask mandates that plagued the country for several years during the "pandemic," scientists at the University of Colorado decided to take a closer look at whether or not fully jabbed people can transfer mRNA-generated antibodies to their fully un-jabbed peers. It turns out that they can.

    Using a combination of tests to detect SARS-CoV-2-specific antibodies in the worn masks of fully jabbed lab members, researchers identified the immune system-produced proteins, which circulate the bloodstream and neutralize foreign substances such as viruses and bacteria.

    "Consistent with results reported by others, the researchers identified both immunoglobulin G (IgG) and immunoglobulin A (IgA) antibodies in the saliva of vaccinated individuals and on their masks," reports explain.

    "Based on their observations, the researchers hypothesized droplet or aerosolized antibody transfer might occur between individuals, similar to how droplets and aerosolized viral particles are transferred by the same route."

    (Related: To "repair heart muscle" damaged by mRNA COVID injections, drug giant Moderna released a second injection, also with mRNA.)

    COVID jab "shedding" delivers "passive immunization" to the unvaccinated

    To test their hypothesis, researchers obtained and compared nasal swabs from non-jabbed children living in fully jabbed, fully non-jabbed, and COVID-positive households. Based on this, they learned that high IgG in the noses of fully jabbed parents was "significantly associated" with an increase in intranasal IgG in fully non-jabbed children from the same household.

    Comparatively, nasal swabs obtained from children living in fully non-jabbed households, meaning nobody in the family got injected for COVID, showed a "complete deficit of SARS-CoV-2-specific antibody detected."

    "In other words, their findings suggest aerosol transmission of antibodies can occur between COVID-19 vaccinated parents and their children – and the tendency for this transfer is directly related to the amount of nasal or oral antibodies found in those who received vaccines," reports explain.

    What this research definitively shows is that vaccine "shedding" is very real, and that unvaccinated people are being "passively immunized" by their fully vaccinated friends and family members whenever they are around them breathing in their tainted aerosols.

    "But this would provide minimal immunity for the 'bystanders' based on the fact that the original mRNA vaccines provide so little protection," commented Brian Hooker, chief scientific officer at Children's Health Defense about the lack of protection produced by passive immunization.

    Not only are the fully jabbed not protected from anything related to covid, but so are the fully non-jabbed that they contaminate with antibody-laced aerosols. In the end, everyone gets polluted with the same toxic chemicals that Hooker warns can cause autoimmunity and "all sorts of reactions" in bystanders due to a similar "molecular mimicry between the COVID-19 Ig [immunoglobulin] antibodies and human proteins."

    Other studies have shown that molecular mimicry between foreign molecules and human molecules can produce an autoimmune response that causes antibodies to function incorrectly and to interact against human proteins.

    If these Ig antibodies can transmit from person to person through aerosols, then there is no reason to believe that spike proteins generated by COVID injections cannot be transmitted as well, Hooker says.

    "This could cause immunization of the bystanders as well as problems associated with spike protein toxicity to bloodstream components and other tissues," he explained.

    According to French pharmacist and biologist Helene Banoun, spike proteins manufactured by the body after it is jabbed for COVID circulate as exosomes, or extracellular vesicles released from cells that transport spike protein through circulation.

    There is never a good reason to get injected for COVID. Learn more at Vaccines.news.

    Sources for this article include:

    TheEpochTimes.com

    Newstarget.com


    mRNA COVID jabs found to spread from vaccinated to unvaccinated via AEROSOLS

    https://www.naturalnews.com/2023-08-04-mrna-covid-vaccines-spread-vaccinated-unvaccinated-aerosols.html
    mRNA COVID jabs found to spread from vaccinated to unvaccinated via AEROSOLS New peer-reviewed research published in the journal ImmunoHorizons shows that individuals who have been "vaccinated" for the Wuhan coronavirus (COVID-19) can spread antibodies generated by the injections to unvaccinated individuals through aerosols. Because of the lengthy mask mandates that plagued the country for several years during the "pandemic," scientists at the University of Colorado decided to take a closer look at whether or not fully jabbed people can transfer mRNA-generated antibodies to their fully un-jabbed peers. It turns out that they can. Using a combination of tests to detect SARS-CoV-2-specific antibodies in the worn masks of fully jabbed lab members, researchers identified the immune system-produced proteins, which circulate the bloodstream and neutralize foreign substances such as viruses and bacteria. "Consistent with results reported by others, the researchers identified both immunoglobulin G (IgG) and immunoglobulin A (IgA) antibodies in the saliva of vaccinated individuals and on their masks," reports explain. "Based on their observations, the researchers hypothesized droplet or aerosolized antibody transfer might occur between individuals, similar to how droplets and aerosolized viral particles are transferred by the same route." (Related: To "repair heart muscle" damaged by mRNA COVID injections, drug giant Moderna released a second injection, also with mRNA.) COVID jab "shedding" delivers "passive immunization" to the unvaccinated To test their hypothesis, researchers obtained and compared nasal swabs from non-jabbed children living in fully jabbed, fully non-jabbed, and COVID-positive households. Based on this, they learned that high IgG in the noses of fully jabbed parents was "significantly associated" with an increase in intranasal IgG in fully non-jabbed children from the same household. Comparatively, nasal swabs obtained from children living in fully non-jabbed households, meaning nobody in the family got injected for COVID, showed a "complete deficit of SARS-CoV-2-specific antibody detected." "In other words, their findings suggest aerosol transmission of antibodies can occur between COVID-19 vaccinated parents and their children – and the tendency for this transfer is directly related to the amount of nasal or oral antibodies found in those who received vaccines," reports explain. What this research definitively shows is that vaccine "shedding" is very real, and that unvaccinated people are being "passively immunized" by their fully vaccinated friends and family members whenever they are around them breathing in their tainted aerosols. "But this would provide minimal immunity for the 'bystanders' based on the fact that the original mRNA vaccines provide so little protection," commented Brian Hooker, chief scientific officer at Children's Health Defense about the lack of protection produced by passive immunization. Not only are the fully jabbed not protected from anything related to covid, but so are the fully non-jabbed that they contaminate with antibody-laced aerosols. In the end, everyone gets polluted with the same toxic chemicals that Hooker warns can cause autoimmunity and "all sorts of reactions" in bystanders due to a similar "molecular mimicry between the COVID-19 Ig [immunoglobulin] antibodies and human proteins." Other studies have shown that molecular mimicry between foreign molecules and human molecules can produce an autoimmune response that causes antibodies to function incorrectly and to interact against human proteins. If these Ig antibodies can transmit from person to person through aerosols, then there is no reason to believe that spike proteins generated by COVID injections cannot be transmitted as well, Hooker says. "This could cause immunization of the bystanders as well as problems associated with spike protein toxicity to bloodstream components and other tissues," he explained. According to French pharmacist and biologist Helene Banoun, spike proteins manufactured by the body after it is jabbed for COVID circulate as exosomes, or extracellular vesicles released from cells that transport spike protein through circulation. There is never a good reason to get injected for COVID. Learn more at Vaccines.news. Sources for this article include: TheEpochTimes.com Newstarget.com mRNA COVID jabs found to spread from vaccinated to unvaccinated via AEROSOLS https://www.naturalnews.com/2023-08-04-mrna-covid-vaccines-spread-vaccinated-unvaccinated-aerosols.html
    WWW.NATURALNEWS.COM
    mRNA COVID jabs found to spread from vaccinated to unvaccinated via AEROSOLS – NaturalNews.com
    New peer-reviewed research published in the journal ImmunoHorizons shows that individuals who have been “vaccinated” for the Wuhan coronavirus (COVID-19) can spread antibodies generated by the injections to unvaccinated individuals through aerosols. Because of the lengthy mask mandates that plagued the country for several years during the “pandemic,” scientists at the University of Colorado decided […]
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  • What is a Vaccine? Is Prophylactic Ivermectin a vaccine?
    Fun with Words!

    Sage Hana
    Air Lift Underground

    It's not the prophylaxis which makes a "vaccine". It's the presumed immune effect from an analogue of the pathogenic agent.

    I always thought "vaccine" also meant stopped infection and transmission.

    But I sure learned better with COVID.

    Vaccine also came to mean: “stops or limits severe disease”. Like a treatment. Or at least that’s how the Gleaming Talking Heads seemed to be moving the goalposts.

    Thanks Animal Farm Napoleons.

    Analogue: something that is similar or comparable to something else either in general or in some specific detail : something that is analogous to something else

    A quick trip to Mockingbird Animal Farm Dictionary has broadened the definition.

    Now it just seems to mean stimulates an immune response.

    Vaccine: a preparation that is administered (as by injection) to stimulate the body's immune response against a specific infectious agent or disease: such as:

    (note Merriam-Webster then provides examples but does not say, “limited to” putting parameters on their taxonomy, so the floodgates are going to open up and all those MAGAMectinInjections and Nasal Sprays may qualify!)


    And then we get to definition #2:

    : a preparation or immunotherapy that is used to stimulate the body's immune response against noninfectious substances, agents, or diseases

    The U.S. Army is also testing a ricin vaccineand has reported success in mice.—Sue Goetinck Ambrose

    … many of the most promising new cancer vaccines use dendritic cells to train the immune system to recognize tumor cells.—Patrick Barry

    Boy you can just see the shitfuckery brewing here, huh?

    Vaccines for anything.

    Tight Psoas?

    There is a vaccine for that!

    Klimate Change?

    Klimate Vaccine.

    Too Many People?

    Try the Herd-Culling Vaccine, aka all of them probs.

    vaccine

    noun

    vac·​cine vak-ˈsēn

    ˈvak-ˌsēn

    pluralvaccines

    1

    : a preparation that is administered (as by injection) to stimulate the body's immune response against a specific infectious agent or disease: such as

    a

    : an antigenic preparation of a typically inactivated or attenuated (see ATTENUATED sense 2) pathogenic agent (such as a bacterium or virus) or one of its components or products (such as a protein or toxin)

    a trivalent influenza vaccine

    oral polio vaccine

    Many vaccines are made from the virus itself, either weakened or killed, which will induce antibodies to bind and kill a live virus. Measles vaccines are just that, weakened (or attenuated) measles viruses.—Ann Finkbeiner et al.

    … a tetanus toxoid-containing vaccinemight be recommended for wound management in a pregnant woman if [greater than or equal to] 5 years have elapsed … .—Mark Sawyer et al.

    In addition the subunit used in a vaccinemust be carefully chosen, because not all components of a pathogen represent beneficial immunological targets.—Thomas J. Matthews and Dani P. Bolognesi

    b

    : a preparation of genetic material (such as a strand of synthesized messenger RNA) that is used by the cells of the body to produce an antigenic substance (such as a fragment of virus spike protein)

    … Moderna's coronavirus vaccine … works by injecting a small piece of mRNA from the coronavirus that codes for the virus' spike protein. … mRNA vaccine spurs the body to produce the spike protein internally. That, in turn, triggers an immune response.—Susie Neilson et al.

    The revolutionary messenger RNA vaccines that are now available have been over a decade in development. … Messenger RNA enters the cell cytoplasm and produces protein from the spike of the Covid-19 virus.—Thomas F. Cozza

    Viral vector vaccines, another recent type of vaccine, are similar to DNA and RNA vaccines, but the virus's genetic information is housed in an attenuated virus (unrelated to the disease-causing virus) that helps to promote host cell fusion and entry.—Priya Kaur

    NOTE: Vaccines may contain adjuvants(such as aluminum hydroxide) designed to enhance the strength and duration of the body's immune response.

    2

    : a preparation or immunotherapy that is used to stimulate the body's immune response against noninfectious substances, agents, or diseases

    The U.S. Army is also testing a ricin vaccineand has reported success in mice.—Sue Goetinck Ambrose

    … many of the most promising new cancer vaccines use dendritic cells to train the immune system to recognize tumor cells.—Patrick Barry

    vaccine adjective

    Holy shit, they use Security State Pharm, Moderna in their example sentence.

    You think Moderna is not State Pharm?

    You think we don’t have State Animal Farm InfoControl?

    "Presumed immune effect" from the injected analogue substance is alluded to in the lead definition Merriam-Webster, but only in the convoluted examples.

    And then the second definition opens up the floodgates.

    a preparation or immunotherapy that is used to stimulate the body's immune response against noninfectious substances, agents, or diseases

    Vaccine: a preparation that is administered (as by injection) to stimulate the body's immune response against a specific infectious agent or disease:

    Or…noninfectious disease!

    It's just an effect...like a vaccine, to use Bob's words.

    Skip to :30-:49 if you have Chronic Lusitano Fatigue.


    ----

    But that's the magic of words and doublespeak.

    They can be officially changed. They can be massaged. The message can be tweaked.

    It can be framed as "new technology", a “preparation”.

    To derive the same intended lofty purpose.

    Of course they will not call it a vaccine if you are “anti-vax” and they still need to get drugs in your body, because the "presumed immune effect from the analogue of the pathologic agent" can be derived via another mechanism.

    Just take the drug. Take the drug. Take the New Drug. The "Repurposed" Drug.

    The definition of vaccine can be changed.

    The Thought Terminating Cliche can be changed.

    “prevention of transmission of Covid-19” Signed Pierre Kory.

    Project Director- Study of Incentives to Improve Medicaid Immunization Coverage Rates, NYC Dept. of Health and Centers for Disease Control


    Remember what I said above?

    I always thought "vaccine" also meant stopped infection and transmission.

    “prevention of transmission of Covid-19” Signed Pierre Kory.

    When you heard that, did you think? Cool! I like that!

    I would like to prevent the transmission of Covid-19!

    M-W: Vaccine: a preparation that is administered (as by injection) to stimulate the body's immune response against a specific infectious agent or disease:

    What did you think vaccine meant?

    What is a preparation?



    People love this about me! Words are fun!

    Can I just say? Ever since I’ve been looking into why there is a full court press to get Ivermectin into your bodies, some of the Not a Movement “anti-vaxxers” have exhibited the same talking points as the Blue Pill Covidians Vaccine Maniacs in 2021, with the same fear-based panic of a drowning swimmer fighting off the life raft.

    “You are a bad person and are hurting people and spreading misinformation.”

    Stop exploring this. Keep out.

    https://ko-fi.com/sagehanaproductions64182

    https://www.buymeacoffee.com/sagehanaJ





    https://donshafi911sars-cov-2.blogspot.com/2024/07/what-is-vaccine-is-prophylactic.html
    What is a Vaccine? Is Prophylactic Ivermectin a vaccine? Fun with Words! Sage Hana Air Lift Underground It's not the prophylaxis which makes a "vaccine". It's the presumed immune effect from an analogue of the pathogenic agent. I always thought "vaccine" also meant stopped infection and transmission. But I sure learned better with COVID. Vaccine also came to mean: “stops or limits severe disease”. Like a treatment. Or at least that’s how the Gleaming Talking Heads seemed to be moving the goalposts. Thanks Animal Farm Napoleons. Analogue: something that is similar or comparable to something else either in general or in some specific detail : something that is analogous to something else A quick trip to Mockingbird Animal Farm Dictionary has broadened the definition. Now it just seems to mean stimulates an immune response. Vaccine: a preparation that is administered (as by injection) to stimulate the body's immune response against a specific infectious agent or disease: such as: (note Merriam-Webster then provides examples but does not say, “limited to” putting parameters on their taxonomy, so the floodgates are going to open up and all those MAGAMectinInjections and Nasal Sprays may qualify!) And then we get to definition #2: : a preparation or immunotherapy that is used to stimulate the body's immune response against noninfectious substances, agents, or diseases The U.S. Army is also testing a ricin vaccineand has reported success in mice.—Sue Goetinck Ambrose … many of the most promising new cancer vaccines use dendritic cells to train the immune system to recognize tumor cells.—Patrick Barry Boy you can just see the shitfuckery brewing here, huh? Vaccines for anything. Tight Psoas? There is a vaccine for that! Klimate Change? Klimate Vaccine. Too Many People? Try the Herd-Culling Vaccine, aka all of them probs. vaccine noun vac·​cine vak-ˈsēn ˈvak-ˌsēn pluralvaccines 1 : a preparation that is administered (as by injection) to stimulate the body's immune response against a specific infectious agent or disease: such as a : an antigenic preparation of a typically inactivated or attenuated (see ATTENUATED sense 2) pathogenic agent (such as a bacterium or virus) or one of its components or products (such as a protein or toxin) a trivalent influenza vaccine oral polio vaccine Many vaccines are made from the virus itself, either weakened or killed, which will induce antibodies to bind and kill a live virus. Measles vaccines are just that, weakened (or attenuated) measles viruses.—Ann Finkbeiner et al. … a tetanus toxoid-containing vaccinemight be recommended for wound management in a pregnant woman if [greater than or equal to] 5 years have elapsed … .—Mark Sawyer et al. In addition the subunit used in a vaccinemust be carefully chosen, because not all components of a pathogen represent beneficial immunological targets.—Thomas J. Matthews and Dani P. Bolognesi b : a preparation of genetic material (such as a strand of synthesized messenger RNA) that is used by the cells of the body to produce an antigenic substance (such as a fragment of virus spike protein) … Moderna's coronavirus vaccine … works by injecting a small piece of mRNA from the coronavirus that codes for the virus' spike protein. … mRNA vaccine spurs the body to produce the spike protein internally. That, in turn, triggers an immune response.—Susie Neilson et al. The revolutionary messenger RNA vaccines that are now available have been over a decade in development. … Messenger RNA enters the cell cytoplasm and produces protein from the spike of the Covid-19 virus.—Thomas F. Cozza Viral vector vaccines, another recent type of vaccine, are similar to DNA and RNA vaccines, but the virus's genetic information is housed in an attenuated virus (unrelated to the disease-causing virus) that helps to promote host cell fusion and entry.—Priya Kaur NOTE: Vaccines may contain adjuvants(such as aluminum hydroxide) designed to enhance the strength and duration of the body's immune response. 2 : a preparation or immunotherapy that is used to stimulate the body's immune response against noninfectious substances, agents, or diseases The U.S. Army is also testing a ricin vaccineand has reported success in mice.—Sue Goetinck Ambrose … many of the most promising new cancer vaccines use dendritic cells to train the immune system to recognize tumor cells.—Patrick Barry vaccine adjective Holy shit, they use Security State Pharm, Moderna in their example sentence. You think Moderna is not State Pharm? You think we don’t have State Animal Farm InfoControl? "Presumed immune effect" from the injected analogue substance is alluded to in the lead definition Merriam-Webster, but only in the convoluted examples. And then the second definition opens up the floodgates. a preparation or immunotherapy that is used to stimulate the body's immune response against noninfectious substances, agents, or diseases Vaccine: a preparation that is administered (as by injection) to stimulate the body's immune response against a specific infectious agent or disease: Or…noninfectious disease! It's just an effect...like a vaccine, to use Bob's words. Skip to :30-:49 if you have Chronic Lusitano Fatigue. ---- But that's the magic of words and doublespeak. They can be officially changed. They can be massaged. The message can be tweaked. It can be framed as "new technology", a “preparation”. To derive the same intended lofty purpose. Of course they will not call it a vaccine if you are “anti-vax” and they still need to get drugs in your body, because the "presumed immune effect from the analogue of the pathologic agent" can be derived via another mechanism. Just take the drug. Take the drug. Take the New Drug. The "Repurposed" Drug. The definition of vaccine can be changed. The Thought Terminating Cliche can be changed. “prevention of transmission of Covid-19” Signed Pierre Kory. Project Director- Study of Incentives to Improve Medicaid Immunization Coverage Rates, NYC Dept. of Health and Centers for Disease Control Remember what I said above? I always thought "vaccine" also meant stopped infection and transmission. “prevention of transmission of Covid-19” Signed Pierre Kory. When you heard that, did you think? Cool! I like that! I would like to prevent the transmission of Covid-19! M-W: Vaccine: a preparation that is administered (as by injection) to stimulate the body's immune response against a specific infectious agent or disease: What did you think vaccine meant? What is a preparation? 😅 People love this about me! Words are fun! Can I just say? Ever since I’ve been looking into why there is a full court press to get Ivermectin into your bodies, some of the Not a Movement “anti-vaxxers” have exhibited the same talking points as the Blue Pill Covidians Vaccine Maniacs in 2021, with the same fear-based panic of a drowning swimmer fighting off the life raft. “You are a bad person and are hurting people and spreading misinformation.” Stop exploring this. Keep out. https://ko-fi.com/sagehanaproductions64182 https://www.buymeacoffee.com/sagehanaJ https://donshafi911sars-cov-2.blogspot.com/2024/07/what-is-vaccine-is-prophylactic.html
    DONSHAFI911SARS-COV-2.BLOGSPOT.COM
    donshafi911
    What is a Vaccine? Is Prophylactic Ivermectin a vaccine? Fun with Words! Sage Hana Air Lift Underground It's not the prophylaxis which mak...
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  • NASA: Satanic Hidden Images in Space Photos? Or Coincidence?
    Don't you just hate when you paint a constellation and it accidentally ends up looking like a demon eating a baby?

    http://donshafi911iamthefaceoftruth.blogspot.com/2024/06/nasa-satanic-hidden-images-in-space.html
    NASA: Satanic Hidden Images in Space Photos? Or Coincidence? Don't you just hate when you paint a constellation and it accidentally ends up looking like a demon eating a baby? http://donshafi911iamthefaceoftruth.blogspot.com/2024/06/nasa-satanic-hidden-images-in-space.html
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