• The Tennessee State Senate has taken a definitive stance against the controversial topic of “chemtrails” by passing SB 2691/HB 2063.

    The bill, which aims to ban the intentional release of chemicals into the atmosphere for geoengineering purposes, was sponsored by Representative Monty Fritts (R-Kingston) and Senator Steve Southerland (R-Morristown) and won approval in the Senate on Monday, The Tennessean reported.

    The legislation is predicated on the claim that “it is documented the federal government or other entities acting on the federal government’s behalf or at the federal government’s request may conduct geoengineering experiments by intentionally dispersing chemicals into the atmosphere, and those activities may occur within the State of Tennessee.”

    This new bill seeks to outlaw any such activities, stating that, “The intentional injection, release, or dispersion, by any means, of chemicals, chemical compounds, substances, or apparatus within the borders of this state into the atmosphere with the express purpose of affecting temperature, weather, or the intensity of the sunlight is prohibited.”





    http://donshafi911.blogspot.com/2024/04/tennessee-state-senate-passes-bill.html https://donshafi911.blogspot.com/2024/04/tennessee-state-senate-passes-bill.html?m=1
    The Tennessee State Senate has taken a definitive stance against the controversial topic of “chemtrails” by passing SB 2691/HB 2063. The bill, which aims to ban the intentional release of chemicals into the atmosphere for geoengineering purposes, was sponsored by Representative Monty Fritts (R-Kingston) and Senator Steve Southerland (R-Morristown) and won approval in the Senate on Monday, The Tennessean reported. The legislation is predicated on the claim that “it is documented the federal government or other entities acting on the federal government’s behalf or at the federal government’s request may conduct geoengineering experiments by intentionally dispersing chemicals into the atmosphere, and those activities may occur within the State of Tennessee.” This new bill seeks to outlaw any such activities, stating that, “The intentional injection, release, or dispersion, by any means, of chemicals, chemical compounds, substances, or apparatus within the borders of this state into the atmosphere with the express purpose of affecting temperature, weather, or the intensity of the sunlight is prohibited.” http://donshafi911.blogspot.com/2024/04/tennessee-state-senate-passes-bill.html https://donshafi911.blogspot.com/2024/04/tennessee-state-senate-passes-bill.html?m=1
    Like
    1
    0 Comments 1 Shares 3412 Views
  • Eminent French Geneticist Dr. Alexandra Henrion-Caude, and Top Investigative Reporter Corinne Lalo Expose the mRNA Vaccine Risks and WHO's Controversial Pandemic Power Grab

    "mRNA vaccines are GMOs. And European law was changed in 2020 to be able to allow the arrival of vaccines GMOs, which are mRNA vaccines,"

    "Recently, Kevin McKernan showed that in vaccines, there was not only mRNA but there was also DNA... up to 30%…So that means that if we find DNA in vaccines, it will end up in genomes,"

    https://vk.com/video-177757343_456244085?access_key=1cc4a41e015243b2cf
    Eminent French Geneticist Dr. Alexandra Henrion-Caude, and Top Investigative Reporter Corinne Lalo Expose the mRNA Vaccine Risks and WHO's Controversial Pandemic Power Grab "mRNA vaccines are GMOs. And European law was changed in 2020 to be able to allow the arrival of vaccines GMOs, which are mRNA vaccines," "Recently, Kevin McKernan showed that in vaccines, there was not only mRNA but there was also DNA... up to 30%…So that means that if we find DNA in vaccines, it will end up in genomes," https://vk.com/video-177757343_456244085?access_key=1cc4a41e015243b2cf
    Like
    1
    0 Comments 0 Shares 1749 Views
  • The Tennessee State Senate has taken a definitive stance against the controversial topic of “chemtrails” by passing SB 2691/HB 2063.

    The bill, which aims to ban the intentional release of chemicals into the atmosphere for geoengineering purposes, was sponsored by Representative Monty Fritts (R-Kingston) and Senator Steve Southerland (R-Morristown) and won approval in the Senate on Monday, The Tennessean reported.

    The legislation is predicated on the claim that “it is documented the federal government or other entities acting on the federal government’s behalf or at the federal government’s request may conduct geoengineering experiments by intentionally dispersing chemicals into the atmosphere, and those activities may occur within the State of Tennessee.”

    This new bill seeks to outlaw any such activities, stating that, “The intentional injection, release, or dispersion, by any means, of chemicals, chemical compounds, substances, or apparatus within the borders of this state into the atmosphere with the express purpose of affecting temperature, weather, or the intensity of the sunlight is prohibited.”





    http://donshafi911.blogspot.com/2024/04/tennessee-state-senate-passes-bill.html https://donshafi911.blogspot.com/2024/04/tennessee-state-senate-passes-bill.html?m=1
    The Tennessee State Senate has taken a definitive stance against the controversial topic of “chemtrails” by passing SB 2691/HB 2063. The bill, which aims to ban the intentional release of chemicals into the atmosphere for geoengineering purposes, was sponsored by Representative Monty Fritts (R-Kingston) and Senator Steve Southerland (R-Morristown) and won approval in the Senate on Monday, The Tennessean reported. The legislation is predicated on the claim that “it is documented the federal government or other entities acting on the federal government’s behalf or at the federal government’s request may conduct geoengineering experiments by intentionally dispersing chemicals into the atmosphere, and those activities may occur within the State of Tennessee.” This new bill seeks to outlaw any such activities, stating that, “The intentional injection, release, or dispersion, by any means, of chemicals, chemical compounds, substances, or apparatus within the borders of this state into the atmosphere with the express purpose of affecting temperature, weather, or the intensity of the sunlight is prohibited.” http://donshafi911.blogspot.com/2024/04/tennessee-state-senate-passes-bill.html https://donshafi911.blogspot.com/2024/04/tennessee-state-senate-passes-bill.html?m=1
    0 Comments 0 Shares 3316 Views
  • Newly published documents from the Robert Koch Institute (RKI) show its researchers explicitly warned that their analysis showed lockdowns in Africa showed 'an expected rise in child mortality'.

    'The consequences of the lockdowns are in parts more severe than the virus itself,' the December 2020 report said, with another document dated to October 2020 suggesting that there was 'no evidence' to support that FFP2 medical masks could prevent the spread of Covid.

    But the findings were never made public, despite researchers clearly advocating for the open communication of their research in meeting minutes, with the German government choosing to pursue legislation their own researchers advised against.

    The revelations come after a two-year legal battle between the RKI and German magazine Multipolar, which ultimately won the court case to publish documents that were heavily redacted by the health agency.

    Multipolar has since launched another legal claim in an attempt to secure full access to the unredacted documents, which may conceal a trove of Covid policy recommendations that the RKI and the German government opted not to share with the public.

    http://donshafi911.blogspot.com/2024/04/lockdowns-could-cause-more-harm-than.html
    Newly published documents from the Robert Koch Institute (RKI) show its researchers explicitly warned that their analysis showed lockdowns in Africa showed 'an expected rise in child mortality'. 'The consequences of the lockdowns are in parts more severe than the virus itself,' the December 2020 report said, with another document dated to October 2020 suggesting that there was 'no evidence' to support that FFP2 medical masks could prevent the spread of Covid. But the findings were never made public, despite researchers clearly advocating for the open communication of their research in meeting minutes, with the German government choosing to pursue legislation their own researchers advised against. The revelations come after a two-year legal battle between the RKI and German magazine Multipolar, which ultimately won the court case to publish documents that were heavily redacted by the health agency. Multipolar has since launched another legal claim in an attempt to secure full access to the unredacted documents, which may conceal a trove of Covid policy recommendations that the RKI and the German government opted not to share with the public. http://donshafi911.blogspot.com/2024/04/lockdowns-could-cause-more-harm-than.html
    0 Comments 0 Shares 3471 Views
  • Australia challenged on ‘moral failure’ of weapons trade with Israel
    Regular protests have been taking place outside Australian firms making crucial components for the F-35 fighter jet.

    Ali MC
    Protesters sitting outside the HTA factory in the Melbourne suburbs,. There is a large placard reading 'Stop arming Israel"
    Weekly protests have been taking place for months [Ali MC/Al Jazeera]
    Melbourne, Australia – Israel’s continued assault on Gaza has highlighted a hidden yet crucial component of the world’s weapons manufacturing industry – suburban Australia.

    Tucked away in Melbourne’s industrial north, Heat Treatment Australia (HTA) is an Australian company that plays a vital role in the production of F-35 Joint Strike Fighters; the same model that Israel is using to bomb Gaza.

    Weekly protests of about 200 people have been taking place for months outside the nondescript factory, where heat treatment is applied to strengthen components for the fighter jet a product of US military giant Lockheed Martin.

    While protesters have sometimes brought production to a halt with their pickets, they remain concerned about what’s going on inside factories like HTA.

    “We decided to hold the community picket to disrupt workers, and we were successful in stopping work for the day,” Nathalie Farah, protest organiser with local group Hume for Palestine, told Al Jazeera. “We consider this to be a win.”

    “Australia is absolutely complicit in the genocide that is happening,” said 26-year-old Farah, who is of Syrian and Palestinian origin. “Which is contrary to what the government might have us believe.”

    More than 32,000 Palestinians have been killed since Israel launched its war in Gaza six months ago after Hamas killed more than 1,000 people in a surprise attack on Israel. The war, being investigated as a genocide by the International Court of Justice (ICJ), has left hundreds of thousands on the brink of starvation, according to the United Nations.

    HTA – which did not respond to Al Jazeera for comment – is just one of an increasing number of companies in Australia engaged in the weapons manufacturing industry.

    Community organiser Nathalie Farah. She's wearing a Palestinian scarf and a black T-shirt saying Australia.
    Nathalie Farah has been organising regular protests outside HTA’s factory [Ali MC/Al Jazeera]
    According to Lockheed Martin, “Every F-35 built contains some Australian parts and components,” with more than 70 Australian companies having export contracts valued at a total 4.13 billion Australian dollars ($2.69bn).

    Protesters have also picketed Rosebank Engineering, in Melbourne’s southeast, the world’s only producer of the F-35’s “uplock actuator system”, a crucial component of the aircraft’s bomb bay doors.

    Sign up for Al Jazeera

    Weekly Newsletter


    protected by reCAPTCHA
    Defence industry push

    In recent years, the Australian government has sought to increase defence exports to boost the country’s flagging manufacturing industry.

    In 2018, former Prime Minister Malcolm Turnbull announced Australia aimed to become one of the world’s top 10 defence exporters within a decade. It is currently 30th in global arms production, according to the Stockholm International Peace Institute.

    It is an aspiration that appears set to continue under the government of Anthony Albanese after it concluded a more than one-billion-Australian-dollar deal with Germany to supply more than 100 Boxer Heavy Weapon Carrier vehicles in 2023 – Australia’s single biggest defence industry deal.

    Since the Gaza war began, the industry and its business relationship with Israel have come increasingly under the spotlight.

    Last month, Deputy Prime Minister Richard Marles insisted that there were “no exports of weapons from Australia to Israel and there haven’t been for many, many years”.

    However, between 2016 and 2023 the Australian government approved some 322 export permits for military and dual-use equipment to Israel.

    The Department of Foreign Affairs and Trade’s own data – available to the public online – shows that Australian exports of “arms and ammunition” to Israel totalled $15.5 million Australian dollars ($10.1m) over the same period of time.

    Officials now appear to be slowing the export of military equipment to Israel.

    In a recent interview with Australia’s national broadcaster ABC, the Minister for International Development and the Pacific Pat Conroy insisted the country was “not exporting military equipment to Israel” and clarified this meant “military weapons, things like bombs”.

    However, defence exports from Australia fall into two categories, items specifically for military use – such as Boxer Heavy Weapons vehicles for Germany – and so-called ‘dual use’ products, such as radar or communications systems, that can have both civilian and military uses.

    Australia’s Department of Defence did not respond to Al Jazeera’s requests about whether the halt to defence exports to Israel also included dual-use items.

    What is certain is that companies such as HTA and Rosebank Engineering are continuing to manufacture components for the F-35, despite the risk of deployment in what South Africa told the International Court of Justice in December amounted to “genocidal acts“.

    In the Netherlands – where parts for the jet are also manufactured – an appeal court last month ordered the Dutch government to block such exports to Israel citing the risk of breaching international law.

    The Australian government has also come under scrutiny for its lax “end-use controls” on the weapons and components it exports.

    As such, while the F-35 components are exported to US parent company Lockheed Martin, their ultimate use is largely outside Australia’s legal purview.

    Lauren Sanders, senior research fellow on law and the future of war at the University of Queensland, told Al Jazeera that the “on-selling of components and military equipment through third party states is a challenge to global export controls.

    “Once something is out of a state’s control, it becomes more difficult to trace, and to prevent it being passed on to another country,” she said.

    Sanders said Australia’s “end use controls” were deficient in comparison with other exporters such as the United States.

    “The US has hundreds of dedicated staff – with appropriate legal authority to investigate – to chase down potential end-use breaches,” she said.

    “Australia does not have the same kind of end-use controls in place in its legislation, nor does it have the same enforcement resources that the US does.”

    A protester carrying a Palestinian flag at a picket outside an Australian arms company. They have wrapped a Palesinian scarf around their face so only their eyes are visible, Other protesters are behind them. They have placards. Some are sitting on the ground.
    The protesters say they will continue their action until manufacturing of F-35 components is stopped [Ali MC/Al Jazeera]
    In fact, under legislation passed in November 2023, permits for defence goods are no longer required for exports to the United Kingdom and the US under the AUKUS security agreement.

    In a statement, the government argued the exemption would “deliver 614 million [Australian dollars; $401m] in value to the Australian economy over 10 years, by reducing costs to local businesses and unlocking investment opportunities with our AUKUS partners”.

    International law

    This new legislation may provide more opportunities for Australian weapons manufacturers, such as NIOA, a privately owned munitions company that makes bullets at a factory in Benalla, a small rural town in Australia’s southeast.

    The largest supplier of munitions to the Australian Defence Force, NIOA – which did not respond to Al Jazeera for comment – also has aspirations to break into the US weapons market.

    At a recent business conference, CEO Robert Nioa said that “the goal is to establish greater production capabilities in both countries so that Australia can be an alternative source of supply of weapons in times of conflict for the Australian and US militaries”.

    Greens Senator David Shoebridge told Al Jazeera that the government needed to “publicly and immediately refute the plan to become a top 10 global arms dealer and then to provide full transparency on all Australian arms exports including end users.

    “While governments in the Netherlands and the UK are facing legal challenges because of their role in the global supply chain, the Australian Labor government just keeps handing over weapons parts as though no genocide was happening,” he said. “It’s an appalling moral failure, and it is almost certainly a gross breach of international law.”

    The Australian government also recently announced a 917 million Australian dollar ($598m) deal with controversial Israeli company Elbit Systems.

    A court in the Netherlands hearing a case brought in relation to military exports. The room is wood panelled and there is a portrait on the wall.
    The Dutch government has faced legal action over the export of F-35 fighter jet parts to Israel [File: Piroschka van de Wouw/Reuters]
    Elbit has come under fire for its sale of defence equipment to the Myanmar military regime, continuing sales even after the military, which seized power in a 2021 coup, was accused of gross human rights violations – including attacks on civilians – by the United Nations and others.

    Despite a recent joint announcement between the Australian and UK governments for an “immediate cessation of fighting” in Gaza, some say Australia needs to go further and cut defence ties with Israel altogether.

    “The Australian government must listen to the growing public calls for peace and end Australia’s two-way arms trade with Israel,” Shoebridge said. “The Albanese government is rewarding and financing the Israeli arms industry just at the moment they are arming a genocide.”

    Protests have continued both at the HTA factory in Melbourne and their premises in Brisbane, with organisers pledging to continue until the company stops manufacturing components for the F-35.

    https://www.aljazeera.com/news/2024/3/28/australia-challenged-on-moral-failure-of-weapons-trade-with-israel
    Australia challenged on ‘moral failure’ of weapons trade with Israel Regular protests have been taking place outside Australian firms making crucial components for the F-35 fighter jet. Ali MC Protesters sitting outside the HTA factory in the Melbourne suburbs,. There is a large placard reading 'Stop arming Israel" Weekly protests have been taking place for months [Ali MC/Al Jazeera] Melbourne, Australia – Israel’s continued assault on Gaza has highlighted a hidden yet crucial component of the world’s weapons manufacturing industry – suburban Australia. Tucked away in Melbourne’s industrial north, Heat Treatment Australia (HTA) is an Australian company that plays a vital role in the production of F-35 Joint Strike Fighters; the same model that Israel is using to bomb Gaza. Weekly protests of about 200 people have been taking place for months outside the nondescript factory, where heat treatment is applied to strengthen components for the fighter jet a product of US military giant Lockheed Martin. While protesters have sometimes brought production to a halt with their pickets, they remain concerned about what’s going on inside factories like HTA. “We decided to hold the community picket to disrupt workers, and we were successful in stopping work for the day,” Nathalie Farah, protest organiser with local group Hume for Palestine, told Al Jazeera. “We consider this to be a win.” “Australia is absolutely complicit in the genocide that is happening,” said 26-year-old Farah, who is of Syrian and Palestinian origin. “Which is contrary to what the government might have us believe.” More than 32,000 Palestinians have been killed since Israel launched its war in Gaza six months ago after Hamas killed more than 1,000 people in a surprise attack on Israel. The war, being investigated as a genocide by the International Court of Justice (ICJ), has left hundreds of thousands on the brink of starvation, according to the United Nations. HTA – which did not respond to Al Jazeera for comment – is just one of an increasing number of companies in Australia engaged in the weapons manufacturing industry. Community organiser Nathalie Farah. She's wearing a Palestinian scarf and a black T-shirt saying Australia. Nathalie Farah has been organising regular protests outside HTA’s factory [Ali MC/Al Jazeera] According to Lockheed Martin, “Every F-35 built contains some Australian parts and components,” with more than 70 Australian companies having export contracts valued at a total 4.13 billion Australian dollars ($2.69bn). Protesters have also picketed Rosebank Engineering, in Melbourne’s southeast, the world’s only producer of the F-35’s “uplock actuator system”, a crucial component of the aircraft’s bomb bay doors. Sign up for Al Jazeera Weekly Newsletter protected by reCAPTCHA Defence industry push In recent years, the Australian government has sought to increase defence exports to boost the country’s flagging manufacturing industry. In 2018, former Prime Minister Malcolm Turnbull announced Australia aimed to become one of the world’s top 10 defence exporters within a decade. It is currently 30th in global arms production, according to the Stockholm International Peace Institute. It is an aspiration that appears set to continue under the government of Anthony Albanese after it concluded a more than one-billion-Australian-dollar deal with Germany to supply more than 100 Boxer Heavy Weapon Carrier vehicles in 2023 – Australia’s single biggest defence industry deal. Since the Gaza war began, the industry and its business relationship with Israel have come increasingly under the spotlight. Last month, Deputy Prime Minister Richard Marles insisted that there were “no exports of weapons from Australia to Israel and there haven’t been for many, many years”. However, between 2016 and 2023 the Australian government approved some 322 export permits for military and dual-use equipment to Israel. The Department of Foreign Affairs and Trade’s own data – available to the public online – shows that Australian exports of “arms and ammunition” to Israel totalled $15.5 million Australian dollars ($10.1m) over the same period of time. Officials now appear to be slowing the export of military equipment to Israel. In a recent interview with Australia’s national broadcaster ABC, the Minister for International Development and the Pacific Pat Conroy insisted the country was “not exporting military equipment to Israel” and clarified this meant “military weapons, things like bombs”. However, defence exports from Australia fall into two categories, items specifically for military use – such as Boxer Heavy Weapons vehicles for Germany – and so-called ‘dual use’ products, such as radar or communications systems, that can have both civilian and military uses. Australia’s Department of Defence did not respond to Al Jazeera’s requests about whether the halt to defence exports to Israel also included dual-use items. What is certain is that companies such as HTA and Rosebank Engineering are continuing to manufacture components for the F-35, despite the risk of deployment in what South Africa told the International Court of Justice in December amounted to “genocidal acts“. In the Netherlands – where parts for the jet are also manufactured – an appeal court last month ordered the Dutch government to block such exports to Israel citing the risk of breaching international law. The Australian government has also come under scrutiny for its lax “end-use controls” on the weapons and components it exports. As such, while the F-35 components are exported to US parent company Lockheed Martin, their ultimate use is largely outside Australia’s legal purview. Lauren Sanders, senior research fellow on law and the future of war at the University of Queensland, told Al Jazeera that the “on-selling of components and military equipment through third party states is a challenge to global export controls. “Once something is out of a state’s control, it becomes more difficult to trace, and to prevent it being passed on to another country,” she said. Sanders said Australia’s “end use controls” were deficient in comparison with other exporters such as the United States. “The US has hundreds of dedicated staff – with appropriate legal authority to investigate – to chase down potential end-use breaches,” she said. “Australia does not have the same kind of end-use controls in place in its legislation, nor does it have the same enforcement resources that the US does.” A protester carrying a Palestinian flag at a picket outside an Australian arms company. They have wrapped a Palesinian scarf around their face so only their eyes are visible, Other protesters are behind them. They have placards. Some are sitting on the ground. The protesters say they will continue their action until manufacturing of F-35 components is stopped [Ali MC/Al Jazeera] In fact, under legislation passed in November 2023, permits for defence goods are no longer required for exports to the United Kingdom and the US under the AUKUS security agreement. In a statement, the government argued the exemption would “deliver 614 million [Australian dollars; $401m] in value to the Australian economy over 10 years, by reducing costs to local businesses and unlocking investment opportunities with our AUKUS partners”. International law This new legislation may provide more opportunities for Australian weapons manufacturers, such as NIOA, a privately owned munitions company that makes bullets at a factory in Benalla, a small rural town in Australia’s southeast. The largest supplier of munitions to the Australian Defence Force, NIOA – which did not respond to Al Jazeera for comment – also has aspirations to break into the US weapons market. At a recent business conference, CEO Robert Nioa said that “the goal is to establish greater production capabilities in both countries so that Australia can be an alternative source of supply of weapons in times of conflict for the Australian and US militaries”. Greens Senator David Shoebridge told Al Jazeera that the government needed to “publicly and immediately refute the plan to become a top 10 global arms dealer and then to provide full transparency on all Australian arms exports including end users. “While governments in the Netherlands and the UK are facing legal challenges because of their role in the global supply chain, the Australian Labor government just keeps handing over weapons parts as though no genocide was happening,” he said. “It’s an appalling moral failure, and it is almost certainly a gross breach of international law.” The Australian government also recently announced a 917 million Australian dollar ($598m) deal with controversial Israeli company Elbit Systems. A court in the Netherlands hearing a case brought in relation to military exports. The room is wood panelled and there is a portrait on the wall. The Dutch government has faced legal action over the export of F-35 fighter jet parts to Israel [File: Piroschka van de Wouw/Reuters] Elbit has come under fire for its sale of defence equipment to the Myanmar military regime, continuing sales even after the military, which seized power in a 2021 coup, was accused of gross human rights violations – including attacks on civilians – by the United Nations and others. Despite a recent joint announcement between the Australian and UK governments for an “immediate cessation of fighting” in Gaza, some say Australia needs to go further and cut defence ties with Israel altogether. “The Australian government must listen to the growing public calls for peace and end Australia’s two-way arms trade with Israel,” Shoebridge said. “The Albanese government is rewarding and financing the Israeli arms industry just at the moment they are arming a genocide.” Protests have continued both at the HTA factory in Melbourne and their premises in Brisbane, with organisers pledging to continue until the company stops manufacturing components for the F-35. https://www.aljazeera.com/news/2024/3/28/australia-challenged-on-moral-failure-of-weapons-trade-with-israel
    WWW.ALJAZEERA.COM
    Australia challenged on ‘moral failure’ of weapons trade with Israel
    Regular protests have been taking place outside Australian firms making crucial components for the F-35 fighter jet.
    Like
    1
    1 Comments 0 Shares 10109 Views
  • BREAKING: Texas Doctors Force FDA to Remove Covid-19 Posts in Settlement

    The U.S. Food and Drug Administration (FDA) has agreed to remove social media posts and webpages that urged people to stop taking ivermectin to treat COVID-19, according to a settlement dated March 21.

    The FDA has already removed a page that said: “Should I take ivermectin to prevent or treat COVID-19? No.”

    Within 21 days, the FDA will remove another page titled, “why you should not use ivermectin to treat or prevent COVID-19,” according to the settlement announcement, which was filed with federal court in southern Texas.

    “The FDA has not authorized or approved ivermectin for use in preventing or treating COVID-19 in humans or animals,” the page currently states. It also says that data do not show ivermectin is effective against COVID-19, despite how some studies it cites show ivermectin is effective against the illness.

    The FDA in the settlement is also agreeing to delete multiple social media posts that came out strongly against ivermectin, including one that stated: “You are not a horse. You are not a cow. Seriously, y’all. Stop it.”

    In exchange, doctors who sued the agency are dismissing their claims, the filing states.

    READ: https://www.ntd.com/fda-settles-ivermectin-case-agrees-to-remove-controversial-stop-it-post_981178.html
    BREAKING: Texas Doctors Force FDA to Remove Covid-19 Posts in Settlement The U.S. Food and Drug Administration (FDA) has agreed to remove social media posts and webpages that urged people to stop taking ivermectin to treat COVID-19, according to a settlement dated March 21. The FDA has already removed a page that said: “Should I take ivermectin to prevent or treat COVID-19? No.” Within 21 days, the FDA will remove another page titled, “why you should not use ivermectin to treat or prevent COVID-19,” according to the settlement announcement, which was filed with federal court in southern Texas. “The FDA has not authorized or approved ivermectin for use in preventing or treating COVID-19 in humans or animals,” the page currently states. It also says that data do not show ivermectin is effective against COVID-19, despite how some studies it cites show ivermectin is effective against the illness. The FDA in the settlement is also agreeing to delete multiple social media posts that came out strongly against ivermectin, including one that stated: “You are not a horse. You are not a cow. Seriously, y’all. Stop it.” In exchange, doctors who sued the agency are dismissing their claims, the filing states. READ: https://www.ntd.com/fda-settles-ivermectin-case-agrees-to-remove-controversial-stop-it-post_981178.html
    WWW.NTD.COM
    FDA Settles Ivermectin Case, Agrees to Remove Controversial ‘Stop It’ Post
    The U.S. Food and Drug Administration (FDA) has agreed to remove social media posts and webpages that urged people to stop taking ivermectin to treat COVID-19, according to a settlement dated March 21. The FDA has already removed a page that said: “Should I take ivermectin to prevent or treat COVID-19? No.” Within 21 days, […]
    Like
    1
    0 Comments 1 Shares 2139 Views
  • FDA Loses its War on Ivermectin: Agrees to Remove All Related Social Media Content and Consumer Advisories on Ivermectin Usage for COVID-19
    by Jim Hᴏft Mar. 22, 2024 8:30 am
    In December 2021, the FDA warned Americans not to use Ivermectin, which “is intended for animals” to treat or prevent COVID-19.

    “Never use medications intended for animals on yourself or other people. Animal ivermectin products are very different from those approved for humans. Use of animal ivermectin for the prevention or treatment of COVID-19 in humans is dangerous,” FDA said at the time.

    This was a very controversial statement at the time since the FDA pushed the drug on African migrants back in 2015, and the drug was praised in several scientific journals.

    There have now been 101 Ivermectin COVID-19 controlled studies that show a 62% lower risk in early treatment in COVID-19 patients.

    New Deals At The Gateway Pundit Discounts Page At MyPillow – Up to 71% Off With Promo Code TGP

    A group of brave doctors had filed a federal lawsuit against the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) over the agencies’ unlawful attempts to block the use of ivermectin in treating COVID-19.

    The lawsuit, filed in the U.S. Southern District of Texas in Galveston, argues that the FDA has overstepped its authority and unjustifiably interfered with their medical practice.

    The plaintiffs, Drs. Mary Talley Bowden, Paul E. Marik, and Robert L. Apter, are contesting the FDA’s portrayal of ivermectin as dangerous for human consumption. They note that the FDA has approved ivermectin for human use since 1996 for a variety of diseases. However, they allege that with the advent of the COVID-19 pandemic, the FDA began releasing documents and social media posts discouraging the use of the anti-viral drug for COVID-19 treatment.

    “We’re suing the FDA for lying to the public about ivermectin,” said Dr. Bowden.

    Claims were made that the initial article misrepresented the law by stating the FDA’s official stance against Ivermectin use without mentioning that doctors were allowed to administer the medicine.

    U.S. law is cited in the complaint, including the provision that the FDA “may not interfere with the authority of a health care provider to prescribe or administer any legally marked device to a patient for any condition or disease within a legitimate health care practitioner-patient relationship.”

    On Thursday, the U.S. Food and Drug Administration (FDA) reportedly agreed to remove all its previous social media posts and consumer advisories that specifically addressed the use of ivermectin for the treatment or prevention of COVID-19.

    “FDA loses its war on ivermectin and agrees to remove all social media posts and consumer directives regarding ivermectin and COVID, including its most popular tweet in FDA history. This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship,” Dr. Bowden wrote on her social media.

    Emily Post News reported:

    The FDA agreed to delete the Twitter, LinkedIn, and Facebook posts from August 21, 2021 that read, “You are not a horse. You are not a cow. Seriously, y’all. Stop it.” (A screencap of the X/twitter one is above and still online here.)

    It will also remove the Twitter post (below) from April 26, 2022 that reads, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.

    Further, the FDA will delete all other social media posts on FDA accounts that link to its website (below) called “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19.”

    It will “retire” this website (called a consumer update) originally posted on March 5, 2021 and revised on September 7, 2021. The FDA retains the right to post a revised update.

    Bowden said she and her co-plaintiffs Dr. Paul E. Marik and Dr. Robert L. Apter decided to drop the lawsuit they got what they wanted.

    “After nearly two years and a resounding rebuke by the Fifth Circuit Court of Appeals, the FDA has agreed to remove its misleading social media posts and consumer directives regarding ivermectin and Covid-19,” said Bowden.

    Trending: MAGA Beauty Isabella DeLuca’s Arrest Is Proof Positive That Biden’s Weaponized Justice System Has Become Outright Despotic Against Political Dissidents


    The Gateway Pundit previously reported that during a hearing, the agency’s lawyers argued that the FDA was only giving advice and it was not mandatory when it told people to “stop” taking Ivermectin for COVID-19.

    “The cited statements were not directives,” said Isaac Belfer, one of the lawyers. “They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.”

    “They use informal language, that is true… It’s conversational but not mandatory,” he continued.

    However, the statement from the lawyer contradicted the FDA’s social media post, stating, “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” and another tweet says, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.”

    Both tweets displayed the title of “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and included a link to that publication.

    Last year, Doctors Mary Talley Bowden, Paul Marik, & Robert Apter appeared in the Fifth Circuit Court of Appeals as part of their lawsuit.

    “The FDA is not your doctor. Yesterday we took them to court to remind them of that,” Dr. Bowden wrote.

    “A pharmacist cites CDC and US FDA as why she will continue to deny filling prescriptions for ivermectin. On Tuesday, the FDA’s attorney declared the FDA has no problem with doctors prescribing ivermectin off-label. It’s time for them to make a formal announcement and set the record straight,” Bowden wrote on Thursday.

    During the oral argument, Ashley Cheung Honold, a Department of Justice lawyer representing the FDA stated that the agency “explicitly recognizes” that doctors do have the authority to administer ivermectin to treat COVID.

    “”FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” said Honold.

    “FDA made these statements in response to multiple reports of consumers being hospitalized, after self-medicating with ivermectin intended for horses, which is available for purchase over the counter without the need for prescription,” Honold said.

    “In some contexts, those words could be construed as a command,” Ms. Honold said. “But in this context, where FDA was simply using these words in the context of a quippy tweet meant to share its informational article, those statements do not rise to the level of a command.”

    “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said.

    It can be recalled that Houston Methodist launched an investigation into Bowden and suspended her for defying health authorities and exercising free speech.

    The hospital excoriated Bowden for “using her social media accounts to express her personal opinions about the COVID-19 vaccine and treatments,” NBC News reports. The suspension barred the physician from admitting or treating patients at the hospital.

    Bowden repeatedly warned that it is “wrong” to mandate the experimental mRNA vaccines and continuously touted Ivermectin as a safe and effective treatment amid threats from public health officials against prescribing the drug.

    Bowden was forced to resign. In her resignation letter, Bowden doubled down on the efficacy of Ivermectin.

    “I have worked hard to provide early treatment for victims of COVID-19. My efforts have been successful. I have treated more than 200 COVID-19 patients, including many with co-morbidities, and none of these patients have required hospitalization. This is a testament to the success of my treatment methods,” she wrote. “Throughout this pandemic, there has been no FDA-approved treatment for COVID. Therefore I have done my best to care for patients and save lives in the absence of a clear scientific consensus.”

    “Early treatment must still be part of any strategy for patient care. That is why physicians and hospitals should pay more attention to medications such as Ivermectin, which significant research and my clinical experience indicate is effective,” she continued. “I have decided to part ways with Houston Methodist because of the accusation that I have been spreading “dangerous information.” This is false and defamatory. I do not spread misinformation, and my opinions are supported by science. There is substantial evidence for the efficacy of Ivermectin in treating COVID-19, and no evidence for serious or fatal side effects associated with the doses used to treat COVID-19.”


    The U.S. FDA was sued over its false statements about ivermectin and now has to remove those false statements from their social media posts https://www.thegatewaypundit.com/2024/03/fda-loses-its-war-ivermectin-agrees-remove-all/. I wonder if the Singapore MOH is following this development.


    FDA Loses its War on Ivermectin: Agrees to Remove All Related Social Media Content and Consumer Advisories on Ivermectin Usage for COVID-19 by Jim Hᴏft Mar. 22, 2024 8:30 am In December 2021, the FDA warned Americans not to use Ivermectin, which “is intended for animals” to treat or prevent COVID-19. “Never use medications intended for animals on yourself or other people. Animal ivermectin products are very different from those approved for humans. Use of animal ivermectin for the prevention or treatment of COVID-19 in humans is dangerous,” FDA said at the time. This was a very controversial statement at the time since the FDA pushed the drug on African migrants back in 2015, and the drug was praised in several scientific journals. There have now been 101 Ivermectin COVID-19 controlled studies that show a 62% lower risk in early treatment in COVID-19 patients. New Deals At The Gateway Pundit Discounts Page At MyPillow – Up to 71% Off With Promo Code TGP A group of brave doctors had filed a federal lawsuit against the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) over the agencies’ unlawful attempts to block the use of ivermectin in treating COVID-19. The lawsuit, filed in the U.S. Southern District of Texas in Galveston, argues that the FDA has overstepped its authority and unjustifiably interfered with their medical practice. The plaintiffs, Drs. Mary Talley Bowden, Paul E. Marik, and Robert L. Apter, are contesting the FDA’s portrayal of ivermectin as dangerous for human consumption. They note that the FDA has approved ivermectin for human use since 1996 for a variety of diseases. However, they allege that with the advent of the COVID-19 pandemic, the FDA began releasing documents and social media posts discouraging the use of the anti-viral drug for COVID-19 treatment. “We’re suing the FDA for lying to the public about ivermectin,” said Dr. Bowden. Claims were made that the initial article misrepresented the law by stating the FDA’s official stance against Ivermectin use without mentioning that doctors were allowed to administer the medicine. U.S. law is cited in the complaint, including the provision that the FDA “may not interfere with the authority of a health care provider to prescribe or administer any legally marked device to a patient for any condition or disease within a legitimate health care practitioner-patient relationship.” On Thursday, the U.S. Food and Drug Administration (FDA) reportedly agreed to remove all its previous social media posts and consumer advisories that specifically addressed the use of ivermectin for the treatment or prevention of COVID-19. “FDA loses its war on ivermectin and agrees to remove all social media posts and consumer directives regarding ivermectin and COVID, including its most popular tweet in FDA history. This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship,” Dr. Bowden wrote on her social media. Emily Post News reported: The FDA agreed to delete the Twitter, LinkedIn, and Facebook posts from August 21, 2021 that read, “You are not a horse. You are not a cow. Seriously, y’all. Stop it.” (A screencap of the X/twitter one is above and still online here.) It will also remove the Twitter post (below) from April 26, 2022 that reads, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19. Further, the FDA will delete all other social media posts on FDA accounts that link to its website (below) called “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19.” It will “retire” this website (called a consumer update) originally posted on March 5, 2021 and revised on September 7, 2021. The FDA retains the right to post a revised update. Bowden said she and her co-plaintiffs Dr. Paul E. Marik and Dr. Robert L. Apter decided to drop the lawsuit they got what they wanted. “After nearly two years and a resounding rebuke by the Fifth Circuit Court of Appeals, the FDA has agreed to remove its misleading social media posts and consumer directives regarding ivermectin and Covid-19,” said Bowden. Trending: MAGA Beauty Isabella DeLuca’s Arrest Is Proof Positive That Biden’s Weaponized Justice System Has Become Outright Despotic Against Political Dissidents The Gateway Pundit previously reported that during a hearing, the agency’s lawyers argued that the FDA was only giving advice and it was not mandatory when it told people to “stop” taking Ivermectin for COVID-19. “The cited statements were not directives,” said Isaac Belfer, one of the lawyers. “They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.” “They use informal language, that is true… It’s conversational but not mandatory,” he continued. However, the statement from the lawyer contradicted the FDA’s social media post, stating, “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” and another tweet says, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.” Both tweets displayed the title of “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and included a link to that publication. Last year, Doctors Mary Talley Bowden, Paul Marik, & Robert Apter appeared in the Fifth Circuit Court of Appeals as part of their lawsuit. “The FDA is not your doctor. Yesterday we took them to court to remind them of that,” Dr. Bowden wrote. “A pharmacist cites CDC and US FDA as why she will continue to deny filling prescriptions for ivermectin. On Tuesday, the FDA’s attorney declared the FDA has no problem with doctors prescribing ivermectin off-label. It’s time for them to make a formal announcement and set the record straight,” Bowden wrote on Thursday. During the oral argument, Ashley Cheung Honold, a Department of Justice lawyer representing the FDA stated that the agency “explicitly recognizes” that doctors do have the authority to administer ivermectin to treat COVID. “”FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” said Honold. “FDA made these statements in response to multiple reports of consumers being hospitalized, after self-medicating with ivermectin intended for horses, which is available for purchase over the counter without the need for prescription,” Honold said. “In some contexts, those words could be construed as a command,” Ms. Honold said. “But in this context, where FDA was simply using these words in the context of a quippy tweet meant to share its informational article, those statements do not rise to the level of a command.” “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said. It can be recalled that Houston Methodist launched an investigation into Bowden and suspended her for defying health authorities and exercising free speech. The hospital excoriated Bowden for “using her social media accounts to express her personal opinions about the COVID-19 vaccine and treatments,” NBC News reports. The suspension barred the physician from admitting or treating patients at the hospital. Bowden repeatedly warned that it is “wrong” to mandate the experimental mRNA vaccines and continuously touted Ivermectin as a safe and effective treatment amid threats from public health officials against prescribing the drug. Bowden was forced to resign. In her resignation letter, Bowden doubled down on the efficacy of Ivermectin. “I have worked hard to provide early treatment for victims of COVID-19. My efforts have been successful. I have treated more than 200 COVID-19 patients, including many with co-morbidities, and none of these patients have required hospitalization. This is a testament to the success of my treatment methods,” she wrote. “Throughout this pandemic, there has been no FDA-approved treatment for COVID. Therefore I have done my best to care for patients and save lives in the absence of a clear scientific consensus.” “Early treatment must still be part of any strategy for patient care. That is why physicians and hospitals should pay more attention to medications such as Ivermectin, which significant research and my clinical experience indicate is effective,” she continued. “I have decided to part ways with Houston Methodist because of the accusation that I have been spreading “dangerous information.” This is false and defamatory. I do not spread misinformation, and my opinions are supported by science. There is substantial evidence for the efficacy of Ivermectin in treating COVID-19, and no evidence for serious or fatal side effects associated with the doses used to treat COVID-19.” The U.S. FDA was sued over its false statements about ivermectin and now has to remove those false statements from their social media posts https://www.thegatewaypundit.com/2024/03/fda-loses-its-war-ivermectin-agrees-remove-all/. I wonder if the Singapore MOH is following this development.
    0 Comments 0 Shares 9572 Views
  • Lawsuit Drops Bombshell on FDA’s Orwellian Lie About Ivermectin
    The FDA has lost its war on ivermectin and agreed to remove all related social media content and consumer advisories on ivermectin usage for COVID-19.

    vnninfluencersMarch 22, 2024
    This article originally appeared on The Gateway Pundit and was republished with permission.

    Guest post by Jim Hᴏft

    In December 2021, the FDA warned Americans not to use Ivermectin, which “is intended for animals” to treat or prevent COVID-19.

    “Never use medications intended for animals on yourself or other people. Animal ivermectin products are very different from those approved for humans. Use of animal ivermectin for the prevention or treatment of COVID-19 in humans is dangerous,” FDA said at the time.

    This was a very controversial statement at the time since the FDA pushed the drug on African migrants back in 2015, and the drug was praised in several scientific journals.

    There have now been 101 Ivermectin COVID-19 controlled studies that show a 62% lower risk in early treatment in COVID-19 patients.



    A group of brave doctors had filed a federal lawsuit against the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) over the agencies’ unlawful attempts to block the use of ivermectin in treating COVID-19.

    The lawsuit, filed in the U.S. Southern District of Texas in Galveston, argues that the FDA has overstepped its authority and unjustifiably interfered with their medical practice.

    The plaintiffs, Drs. Mary Talley Bowden, Paul E. Marik, and Robert L. Apter, are contesting the FDA’s portrayal of ivermectin as dangerous for human consumption. They note that the FDA has approved ivermectin for human use since 1996 for a variety of diseases. However, they allege that with the advent of the COVID-19 pandemic, the FDA began releasing documents and social media posts discouraging the use of the anti-viral drug for COVID-19 treatment.

    “We’re suing the FDA for lying to the public about ivermectin,” said Dr. Bowden.

    Claims were made that the initial article misrepresented the law by stating the FDA’s official stance against Ivermectin use without mentioning that doctors were allowed to administer the medicine.

    U.S. law is cited in the complaint, including the provision that the FDA “may not interfere with the authority of a health care provider to prescribe or administer any legally marked device to a patient for any condition or disease within a legitimate health care practitioner-patient relationship.”

    On Thursday, the U.S. Food and Drug Administration (FDA) reportedly agreed to remove all its previous social media posts and consumer advisories that specifically addressed the use of ivermectin for the treatment or prevention of COVID-19.

    “FDA loses its war on ivermectin and agrees to remove all social media posts and consumer directives regarding ivermectin and COVID, including its most popular tweet in FDA history. This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship,” Dr. Bowden wrote on her social media.

    The plaintiffs have recently received the signed court order and are preparing to issue a press release about it later today.


    The Gateway Pundit previously reported that during a hearing, the agency’s lawyers argued that the FDA was only giving advice and it was not mandatory when it told people to “stop” taking Ivermectin for COVID-19.

    “The cited statements were not directives,” said Isaac Belfer, one of the lawyers. “They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.”

    “They use informal language, that is true… It’s conversational but not mandatory,” he continued.

    However, the statement from the lawyer contradicted the FDA’s social media post, stating, “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” and another tweet says, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.”

    Both tweets displayed the title of “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and included a link to that publication.




    Last year, Doctors Mary Talley Bowden, Paul Marik, & Robert Apter appeared in the Fifth Circuit Court of Appeals as part of their lawsuit.

    “The FDA is not your doctor. Yesterday we took them to court to remind them of that,” Dr. Bowden wrote.

    “A pharmacist cites CDC and US FDA as why she will continue to deny filling prescriptions for ivermectin. On Tuesday, the FDA’s attorney declared the FDA has no problem with doctors prescribing ivermectin off-label. It’s time for them to make a formal announcement and set the record straight,” Bowden wrote on Thursday.

    During the oral argument, Ashley Cheung Honold, a Department of Justice lawyer representing the FDA stated that the agency “explicitly recognizes” that doctors do have the authority to administer ivermectin to treat COVID.

    “”FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” said Honold.

    “FDA made these statements in response to multiple reports of consumers being hospitalized, after self-medicating with ivermectin intended for horses, which is available for purchase over the counter without the need for prescription,” Honold said.

    “In some contexts, those words could be construed as a command,” Ms. Honold said. “But in this context, where FDA was simply using these words in the context of a quippy tweet meant to share its informational article, those statements do not rise to the level of a command.”

    “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said.

    It can be recalled that Houston Methodist launched an investigation into Bowden and suspended her for defying health authorities and exercising free speech.

    The hospital excoriated Bowden for “using her social media accounts to express her personal opinions about the COVID-19 vaccine and treatments,” NBC News reports. The suspension barred the physician from admitting or treating patients at the hospital.

    Bowden repeatedly warned that it is “wrong” to mandate the experimental mRNA vaccines and continuously touted Ivermectin as a safe and effective treatment amid threats from public health officials against prescribing the drug.

    Bowden was forced to resign. In her resignation letter, Bowden doubled down on the efficacy of Ivermectin.

    “I have worked hard to provide early treatment for victims of COVID-19. My efforts have been successful. I have treated more than 200 COVID-19 patients, including many with co-morbidities, and none of these patients have required hospitalization. This is a testament to the success of my treatment methods,” she wrote. “Throughout this pandemic, there has been no FDA-approved treatment for COVID. Therefore I have done my best to care for patients and save lives in the absence of a clear scientific consensus.”

    “Early treatment must still be part of any strategy for patient care. That is why physicians and hospitals should pay more attention to medications such as Ivermectin, which significant research and my clinical experience indicate is effective,” she continued. “I have decided to part ways with Houston Methodist because of the accusation that I have been spreading “dangerous information.” This is false and defamatory. I do not spread misinformation, and my opinions are supported by science. There is substantial evidence for the efficacy of Ivermectin in treating COVID-19, and no evidence for serious or fatal side effects associated with the doses used to treat COVID-19.”

    Copyright 2024 The Gateway Pundit


    https://vigilantnews.com/post/lawsuit-drops-bombshell-on-fdas-orwellian-lie-about-ivermectin/
    Lawsuit Drops Bombshell on FDA’s Orwellian Lie About Ivermectin The FDA has lost its war on ivermectin and agreed to remove all related social media content and consumer advisories on ivermectin usage for COVID-19. vnninfluencersMarch 22, 2024 This article originally appeared on The Gateway Pundit and was republished with permission. Guest post by Jim Hᴏft In December 2021, the FDA warned Americans not to use Ivermectin, which “is intended for animals” to treat or prevent COVID-19. “Never use medications intended for animals on yourself or other people. Animal ivermectin products are very different from those approved for humans. Use of animal ivermectin for the prevention or treatment of COVID-19 in humans is dangerous,” FDA said at the time. This was a very controversial statement at the time since the FDA pushed the drug on African migrants back in 2015, and the drug was praised in several scientific journals. There have now been 101 Ivermectin COVID-19 controlled studies that show a 62% lower risk in early treatment in COVID-19 patients. A group of brave doctors had filed a federal lawsuit against the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) over the agencies’ unlawful attempts to block the use of ivermectin in treating COVID-19. The lawsuit, filed in the U.S. Southern District of Texas in Galveston, argues that the FDA has overstepped its authority and unjustifiably interfered with their medical practice. The plaintiffs, Drs. Mary Talley Bowden, Paul E. Marik, and Robert L. Apter, are contesting the FDA’s portrayal of ivermectin as dangerous for human consumption. They note that the FDA has approved ivermectin for human use since 1996 for a variety of diseases. However, they allege that with the advent of the COVID-19 pandemic, the FDA began releasing documents and social media posts discouraging the use of the anti-viral drug for COVID-19 treatment. “We’re suing the FDA for lying to the public about ivermectin,” said Dr. Bowden. Claims were made that the initial article misrepresented the law by stating the FDA’s official stance against Ivermectin use without mentioning that doctors were allowed to administer the medicine. U.S. law is cited in the complaint, including the provision that the FDA “may not interfere with the authority of a health care provider to prescribe or administer any legally marked device to a patient for any condition or disease within a legitimate health care practitioner-patient relationship.” On Thursday, the U.S. Food and Drug Administration (FDA) reportedly agreed to remove all its previous social media posts and consumer advisories that specifically addressed the use of ivermectin for the treatment or prevention of COVID-19. “FDA loses its war on ivermectin and agrees to remove all social media posts and consumer directives regarding ivermectin and COVID, including its most popular tweet in FDA history. This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship,” Dr. Bowden wrote on her social media. The plaintiffs have recently received the signed court order and are preparing to issue a press release about it later today. The Gateway Pundit previously reported that during a hearing, the agency’s lawyers argued that the FDA was only giving advice and it was not mandatory when it told people to “stop” taking Ivermectin for COVID-19. “The cited statements were not directives,” said Isaac Belfer, one of the lawyers. “They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.” “They use informal language, that is true… It’s conversational but not mandatory,” he continued. However, the statement from the lawyer contradicted the FDA’s social media post, stating, “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” and another tweet says, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.” Both tweets displayed the title of “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and included a link to that publication. Last year, Doctors Mary Talley Bowden, Paul Marik, & Robert Apter appeared in the Fifth Circuit Court of Appeals as part of their lawsuit. “The FDA is not your doctor. Yesterday we took them to court to remind them of that,” Dr. Bowden wrote. “A pharmacist cites CDC and US FDA as why she will continue to deny filling prescriptions for ivermectin. On Tuesday, the FDA’s attorney declared the FDA has no problem with doctors prescribing ivermectin off-label. It’s time for them to make a formal announcement and set the record straight,” Bowden wrote on Thursday. During the oral argument, Ashley Cheung Honold, a Department of Justice lawyer representing the FDA stated that the agency “explicitly recognizes” that doctors do have the authority to administer ivermectin to treat COVID. “”FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” said Honold. “FDA made these statements in response to multiple reports of consumers being hospitalized, after self-medicating with ivermectin intended for horses, which is available for purchase over the counter without the need for prescription,” Honold said. “In some contexts, those words could be construed as a command,” Ms. Honold said. “But in this context, where FDA was simply using these words in the context of a quippy tweet meant to share its informational article, those statements do not rise to the level of a command.” “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said. It can be recalled that Houston Methodist launched an investigation into Bowden and suspended her for defying health authorities and exercising free speech. The hospital excoriated Bowden for “using her social media accounts to express her personal opinions about the COVID-19 vaccine and treatments,” NBC News reports. The suspension barred the physician from admitting or treating patients at the hospital. Bowden repeatedly warned that it is “wrong” to mandate the experimental mRNA vaccines and continuously touted Ivermectin as a safe and effective treatment amid threats from public health officials against prescribing the drug. Bowden was forced to resign. In her resignation letter, Bowden doubled down on the efficacy of Ivermectin. “I have worked hard to provide early treatment for victims of COVID-19. My efforts have been successful. I have treated more than 200 COVID-19 patients, including many with co-morbidities, and none of these patients have required hospitalization. This is a testament to the success of my treatment methods,” she wrote. “Throughout this pandemic, there has been no FDA-approved treatment for COVID. Therefore I have done my best to care for patients and save lives in the absence of a clear scientific consensus.” “Early treatment must still be part of any strategy for patient care. That is why physicians and hospitals should pay more attention to medications such as Ivermectin, which significant research and my clinical experience indicate is effective,” she continued. “I have decided to part ways with Houston Methodist because of the accusation that I have been spreading “dangerous information.” This is false and defamatory. I do not spread misinformation, and my opinions are supported by science. There is substantial evidence for the efficacy of Ivermectin in treating COVID-19, and no evidence for serious or fatal side effects associated with the doses used to treat COVID-19.” Copyright 2024 The Gateway Pundit https://vigilantnews.com/post/lawsuit-drops-bombshell-on-fdas-orwellian-lie-about-ivermectin/
    VIGILANTNEWS.COM
    Lawsuit Drops Bombshell on FDA’s Orwellian Lie About Ivermectin
    The FDA has lost its war on ivermectin and agreed to remove all related social media content and consumer advisories on ivermectin usage for COVID-19.
    1 Comments 0 Shares 7494 Views
  • What a War Requires
    Yes, It's About Resources

    Dr Naomi Wolf

    Dear Readers, Dear Extended Family

    I am grateful that this Substack — which, if you read the comment section, is also one that is a home or meeting-place for many of the most interesting and idealistic people on the Internet — has 83,500 plus subscribers. That is almost the subscriber base of The New Republic. It had 737,000 plus views in the last 30 days — 249,000 plus more than the month prior. That is more views than the number of the audience of CNN.

    Every reader is equally precious to me. But you all count on me — you tell me this — to do all I can to affect national and even global outcomes. From the messages I receive, leaders from all walks of life do indeed read this Substack — and so it is having some impact on the public discussion and perhaps even on public outcomes.

    But this Substack has only a few more than 4000 paid subscribers.

    Why does this matter, more than to my personal finances?

    As you know, I believe — I think at this point it is incontrovertible - that a war is being waged upon us, one that will soon become a “hot war.” My husband Brian O’Shea, who cohosts the podcast “Unrestricted Invasion” with JJ Carrell, is documenting the positioning of military-age or gangland-age illegal-immigrant young men, in barracks-type situations in strategic points around the country. This week he went undercover to a budget hotel in Massachusetts, where security and the hotel staff sought to prevent him from filming what was happening inside in relation to scores of illegal incomers. He was subsequently followed by a maroon sedan that pulled up right as he was leaving the hotel; the drivers proceeded to wait til he was his car, and then followed him across three different exits til he shook them off.

    Brian was also confronted by security, and then followed, earlier this year, when he went to document a facility in Brooklyn, Floyd Bennett Field, an area with over 1000 flat acres of land, where illegal immigrants are being housed in military-style facilities. Illegal immigrants are being housed at Chicago’s O’Hare airport, a sensitive strategic location for a possible attack on America, if there ever was one. Illegal immigrants, disproportionately fighting-age men, are being housed for months in hotels in midtown Manhattan, all basic expenses paid and with cleaning services.

    As they say, wake up and smell the coffee. This is not a domestic policy issue any longer — ie, what are these illegal immigrants getting that your legal immigrant parents or grandparents, your enslaved great-grandparents, did not get? To anyone who has ever been in a combat area, this set of situations depicts what is obviously a military or terrorist set of staging areas. Or, to be conservative, this set of landscapes has all the hallmarks of depicting military or terrorist staging areas.

    Meanwhile, the whips are being brought down on the shoulders of the last standing dissidents in the United States and globally. A Canadian court ordered psychologist and commentator Jordan Peterson to be forced into a re-education program. Literal Marxism. Ethical physician Dr Kulvinder Kaur Gill, who was critical of the mRNA injections, has been hit with a $1 million dollar fine after her libel suit in defense of her reputation, failed. She was forced to mobilize an online donations campaign in order not to lose her house. Under the guise of a credit review, as he points out, researcher and inventor of the mRNA vaccine Dr Robert Malone has been hit with a letter from payment processor Stripe, demanding his bank records. He was told that it will cost $100,000 to fight it. Other dissident voices on Substack, including conservative voices, are being hit in similar ways.

    Governor Hochul declared that National Guard would take on some civil policing roles in New York State, and she is appealing the court decision that prevented her from opening quarantine camps that could detain New Yorkers without trial or even without infection, indefinitely. If she prevails, and if the WHO treaty that declares WHO “pandemic” requirements superior to national or state law prevails in May, the National Guard (or the WHO’s own mercenaries) could show up at any New Yorker’s house, and this is the state where I live; and compel him or her to be transported to a detention facility, and that would be that.

    Why am I presenting all of this to you? Because things are getting very scary and we need your help.

    This Substack does not just provide personal income for me. It is the source of funds to meet costs for the independent news and opinion site DailyClout.io and for BillCam when our demands exceed our resources.

    Gloria Steinem says to look at your checkbook to see if you are walking your talk morally, and my checkbook speaks volumes. I had hoped by the age of 61, after decades of training for my profession, honing my craft as a writer, and fighting for humanity and for humane values, that I would be able to look at my checkbook records and see mostly expenses for travel, with other records perhaps of dinners in some lovely restaurants, an occasional nice dress or two, and funds devoted to caring for elderly relatives.

    But my primary expenditure is not for any of that. Most of the money I earn goes to scrambling to meet the extraordinary and unpredictable costs that running a war from the trenches of DailyClout can involve, and many of these high costs arise unpredictably. Remember, too, that those who use their own resources to oppose and harass us and me personally, include one of the biggest companies in the world, not to mention the United States government, including its justice arm — and state governments. One of our legal letters is against the Justice Department. One of our lawsuits is against the Biden administration, including the CDC.

    Though we are doing impressively well as a startup helmed by three people, and punching far above our weight, we have, as you know, bills that can top six figures for the various lawsuits we are waging on your behalf.

    To keep a dissident news startup — one that also crafts draft bills and passes them, as nonprofits cannot do, which activity involves traversing a minefield of FEC restrictions — so scrupulously kosher that it can’t be brought down by government tripwires, is itself a legal bill for tens of thousands.

    Though we are a lean machine, our technical costs are substantial. Our API, the feed from which our legislative technology that lets you see, share and act on any bill, costs thousands of dollars per quarter. Our developers have created tools — the latest being the extraordinary game changer LegiSector, at https://www.legisector.com (due to suppression, you need to cut and paste the whole url in order to see it) — that sweep away all obfuscation from state and federal legislation, and allow you to pass, share or stop bills from the ease of your own desktop, or even from your handheld. This is also a tens of thousands of dollars a year commitment. As we push to launch this revolutionary tool, Google appears to be suppressing it so thoroughly that it is difficult for us to let the world know that everything has changed now, as interviewers who have covered this tool are telling me, when it comes to legislative transparency. We need a marketing campaign in the tens of thousands to break through this censorship by another one of the biggest companies on Earth.

    It is my sleepless nights, no one else’s, that are involved in trying to figure out how.

    Then there are the fights to protect the reputation that allows me to lead this company and its mission and tools, forward; I was forced to spend tens of thousands on a lawsuit against Twitter for suppressing my (accurate, important) warnings about harms to women from the mRNA injections. My co-plaintiff? President Donald Trump. (Sadly I do not have the resources for legal representation, that my co-plaintiff does.)

    The point of all of the above is that staying credible, meaning fighting the constant government- and nonprofit-sponsored attacks on the credibility of my and my company’s reputations; staying on the right side of all government regulations, so that no harm can come to me or the company; fighting in the courts so that a precedent can be set to protect all Americans from the government leaning on private companies to destroy them — fighting Google’s algorithms with creative workarounds; fighting laws that constantly seek to imprison or bankrupt us — all of this, at times, as you know because I have shared it with you before, can take a terrible financial and psychic/energetic toll.

    It is tempting to just walk away and, to paraphrase Voltaire, “cultivate my own garden.”

    But to stay in these trenches and achieve it at all, all that so many of you tell me you are counting on, requires a robust and reliable stream of resources if we are to stay alive in this culture of lies and erasures.

    Think about the lives we have saved. Maybe yours or your loved ones. Think about whether anyone else’s technology lets you see and act on any state or Federal bill, or protect your investments; with both BillCam and LegiSector offering free searches.

    Think about whether anyone else is soliciting citizens’ input on draft model bills, hiring lawyers, drafting and passing them, in the way we do. Remember, nonprofits can give you a tax deduction, but they cannot lobby. They must stop short of actual political action with legislation and legislators. The fact that we aren’t a nonprofit allows us to lobby and draft and pass bills — a superpower — but makes it much harder for us to raise donation funding.

    Think about this Substack, for that matter. Did my writing help to balance and reassure you in this nightmarish struggle? Did it inform you of important issues that could affect your family? Did you find community and spiritual strength here?

    What would your world be like without my voice, or without DailyClout’s voice and tools and advocacy?

    There would be a lot more darkness, and you and your family’s position and knowledge base would be weakened. I do not think that is too strong a statement.

    If you want these voices and institutions to keep fighting this war, mine but also others’, there is no alternative but to support them with, dare I say it, your actual money.

    I know that many people cannot afford $8 a month. But many of the 83,000 subscribers who are now free, could afford to upgrade to the status of paid subscriber. And the difference between 4 per cent of my readers being paid subscribers and eight per cent being paid subscribers, is the difference between a precarious and easily extinguished position on the battlefield, versus a more secure one that can continue winning victory after victory for you.

    And I will tell you, speaking both as a writer and on behalf of a dissident company, without your financial support it is not only materially unsustainable to fight on, but emotionally unsustainable, as the battles grow more serious and more costly. Without your help, over time, the strain of trying to figure out, during many months, how to pay our lawyers, as well as our API invoices and our developers and our travel to statehouses to lobby for freedom for you, will simply become too great.

    We need your help in spiritual and emotional as well as in material ways.

    You should support us not as a charity but because our our approach works. Because of our draft Five Freedoms bill, which passed in 33 states in 2021, you do not have vaccine passports in the US, and kids went back to school earlier than they might have done. Our Election Integrity bill, which you all shared, has cosponsors in Wyoming, was introduced and defeated in Maine (but a successor has been tapped to re-introduce it in the Fall), and three other states, Michigan, Alabama and North Dakota, have citizens and legislators acting to push it forward. The Pfizer Papers comes out in May. The manuscript, which Amy Kelly and I edited, is 500 pages long. We edited 96 reports from the WarRoom/DailyClout Pfizer Documents Research Team, who in turn had reviewed 450,000 pages of internal Pfizer documents. They revealed the greatest crime against humanity in history in exhaustive detail, affecting people and governments worldwide. Their work is cited or used without citation by dozens of other freedom advocates, and legislators. And booster uptake is now down to 4%; Pfizer’s profits ground to pre-2016 levels.

    We saved, together, with your help, what may turn out to be millions of lives and countless unborn babies.

    But to continue, I need your help; seriously; now just now but into the future.

    If you can afford, it, and if the above is meaningful to you at all, do please upgrade your subscription from free to paid.

    The war is here, and you need warriors fighting for you, who are not barefoot in the snow, but who have warm clothing, and weapons, and ammunition.

    https://naomiwolf.substack.com/p/what-a-war-requires
    What a War Requires Yes, It's About Resources Dr Naomi Wolf Dear Readers, Dear Extended Family I am grateful that this Substack — which, if you read the comment section, is also one that is a home or meeting-place for many of the most interesting and idealistic people on the Internet — has 83,500 plus subscribers. That is almost the subscriber base of The New Republic. It had 737,000 plus views in the last 30 days — 249,000 plus more than the month prior. That is more views than the number of the audience of CNN. Every reader is equally precious to me. But you all count on me — you tell me this — to do all I can to affect national and even global outcomes. From the messages I receive, leaders from all walks of life do indeed read this Substack — and so it is having some impact on the public discussion and perhaps even on public outcomes. But this Substack has only a few more than 4000 paid subscribers. Why does this matter, more than to my personal finances? As you know, I believe — I think at this point it is incontrovertible - that a war is being waged upon us, one that will soon become a “hot war.” My husband Brian O’Shea, who cohosts the podcast “Unrestricted Invasion” with JJ Carrell, is documenting the positioning of military-age or gangland-age illegal-immigrant young men, in barracks-type situations in strategic points around the country. This week he went undercover to a budget hotel in Massachusetts, where security and the hotel staff sought to prevent him from filming what was happening inside in relation to scores of illegal incomers. He was subsequently followed by a maroon sedan that pulled up right as he was leaving the hotel; the drivers proceeded to wait til he was his car, and then followed him across three different exits til he shook them off. Brian was also confronted by security, and then followed, earlier this year, when he went to document a facility in Brooklyn, Floyd Bennett Field, an area with over 1000 flat acres of land, where illegal immigrants are being housed in military-style facilities. Illegal immigrants are being housed at Chicago’s O’Hare airport, a sensitive strategic location for a possible attack on America, if there ever was one. Illegal immigrants, disproportionately fighting-age men, are being housed for months in hotels in midtown Manhattan, all basic expenses paid and with cleaning services. As they say, wake up and smell the coffee. This is not a domestic policy issue any longer — ie, what are these illegal immigrants getting that your legal immigrant parents or grandparents, your enslaved great-grandparents, did not get? To anyone who has ever been in a combat area, this set of situations depicts what is obviously a military or terrorist set of staging areas. Or, to be conservative, this set of landscapes has all the hallmarks of depicting military or terrorist staging areas. Meanwhile, the whips are being brought down on the shoulders of the last standing dissidents in the United States and globally. A Canadian court ordered psychologist and commentator Jordan Peterson to be forced into a re-education program. Literal Marxism. Ethical physician Dr Kulvinder Kaur Gill, who was critical of the mRNA injections, has been hit with a $1 million dollar fine after her libel suit in defense of her reputation, failed. She was forced to mobilize an online donations campaign in order not to lose her house. Under the guise of a credit review, as he points out, researcher and inventor of the mRNA vaccine Dr Robert Malone has been hit with a letter from payment processor Stripe, demanding his bank records. He was told that it will cost $100,000 to fight it. Other dissident voices on Substack, including conservative voices, are being hit in similar ways. Governor Hochul declared that National Guard would take on some civil policing roles in New York State, and she is appealing the court decision that prevented her from opening quarantine camps that could detain New Yorkers without trial or even without infection, indefinitely. If she prevails, and if the WHO treaty that declares WHO “pandemic” requirements superior to national or state law prevails in May, the National Guard (or the WHO’s own mercenaries) could show up at any New Yorker’s house, and this is the state where I live; and compel him or her to be transported to a detention facility, and that would be that. Why am I presenting all of this to you? Because things are getting very scary and we need your help. This Substack does not just provide personal income for me. It is the source of funds to meet costs for the independent news and opinion site DailyClout.io and for BillCam when our demands exceed our resources. Gloria Steinem says to look at your checkbook to see if you are walking your talk morally, and my checkbook speaks volumes. I had hoped by the age of 61, after decades of training for my profession, honing my craft as a writer, and fighting for humanity and for humane values, that I would be able to look at my checkbook records and see mostly expenses for travel, with other records perhaps of dinners in some lovely restaurants, an occasional nice dress or two, and funds devoted to caring for elderly relatives. But my primary expenditure is not for any of that. Most of the money I earn goes to scrambling to meet the extraordinary and unpredictable costs that running a war from the trenches of DailyClout can involve, and many of these high costs arise unpredictably. Remember, too, that those who use their own resources to oppose and harass us and me personally, include one of the biggest companies in the world, not to mention the United States government, including its justice arm — and state governments. One of our legal letters is against the Justice Department. One of our lawsuits is against the Biden administration, including the CDC. Though we are doing impressively well as a startup helmed by three people, and punching far above our weight, we have, as you know, bills that can top six figures for the various lawsuits we are waging on your behalf. To keep a dissident news startup — one that also crafts draft bills and passes them, as nonprofits cannot do, which activity involves traversing a minefield of FEC restrictions — so scrupulously kosher that it can’t be brought down by government tripwires, is itself a legal bill for tens of thousands. Though we are a lean machine, our technical costs are substantial. Our API, the feed from which our legislative technology that lets you see, share and act on any bill, costs thousands of dollars per quarter. Our developers have created tools — the latest being the extraordinary game changer LegiSector, at https://www.legisector.com (due to suppression, you need to cut and paste the whole url in order to see it) — that sweep away all obfuscation from state and federal legislation, and allow you to pass, share or stop bills from the ease of your own desktop, or even from your handheld. This is also a tens of thousands of dollars a year commitment. As we push to launch this revolutionary tool, Google appears to be suppressing it so thoroughly that it is difficult for us to let the world know that everything has changed now, as interviewers who have covered this tool are telling me, when it comes to legislative transparency. We need a marketing campaign in the tens of thousands to break through this censorship by another one of the biggest companies on Earth. It is my sleepless nights, no one else’s, that are involved in trying to figure out how. Then there are the fights to protect the reputation that allows me to lead this company and its mission and tools, forward; I was forced to spend tens of thousands on a lawsuit against Twitter for suppressing my (accurate, important) warnings about harms to women from the mRNA injections. My co-plaintiff? President Donald Trump. (Sadly I do not have the resources for legal representation, that my co-plaintiff does.) The point of all of the above is that staying credible, meaning fighting the constant government- and nonprofit-sponsored attacks on the credibility of my and my company’s reputations; staying on the right side of all government regulations, so that no harm can come to me or the company; fighting in the courts so that a precedent can be set to protect all Americans from the government leaning on private companies to destroy them — fighting Google’s algorithms with creative workarounds; fighting laws that constantly seek to imprison or bankrupt us — all of this, at times, as you know because I have shared it with you before, can take a terrible financial and psychic/energetic toll. It is tempting to just walk away and, to paraphrase Voltaire, “cultivate my own garden.” But to stay in these trenches and achieve it at all, all that so many of you tell me you are counting on, requires a robust and reliable stream of resources if we are to stay alive in this culture of lies and erasures. Think about the lives we have saved. Maybe yours or your loved ones. Think about whether anyone else’s technology lets you see and act on any state or Federal bill, or protect your investments; with both BillCam and LegiSector offering free searches. Think about whether anyone else is soliciting citizens’ input on draft model bills, hiring lawyers, drafting and passing them, in the way we do. Remember, nonprofits can give you a tax deduction, but they cannot lobby. They must stop short of actual political action with legislation and legislators. The fact that we aren’t a nonprofit allows us to lobby and draft and pass bills — a superpower — but makes it much harder for us to raise donation funding. Think about this Substack, for that matter. Did my writing help to balance and reassure you in this nightmarish struggle? Did it inform you of important issues that could affect your family? Did you find community and spiritual strength here? What would your world be like without my voice, or without DailyClout’s voice and tools and advocacy? There would be a lot more darkness, and you and your family’s position and knowledge base would be weakened. I do not think that is too strong a statement. If you want these voices and institutions to keep fighting this war, mine but also others’, there is no alternative but to support them with, dare I say it, your actual money. I know that many people cannot afford $8 a month. But many of the 83,000 subscribers who are now free, could afford to upgrade to the status of paid subscriber. And the difference between 4 per cent of my readers being paid subscribers and eight per cent being paid subscribers, is the difference between a precarious and easily extinguished position on the battlefield, versus a more secure one that can continue winning victory after victory for you. And I will tell you, speaking both as a writer and on behalf of a dissident company, without your financial support it is not only materially unsustainable to fight on, but emotionally unsustainable, as the battles grow more serious and more costly. Without your help, over time, the strain of trying to figure out, during many months, how to pay our lawyers, as well as our API invoices and our developers and our travel to statehouses to lobby for freedom for you, will simply become too great. We need your help in spiritual and emotional as well as in material ways. You should support us not as a charity but because our our approach works. Because of our draft Five Freedoms bill, which passed in 33 states in 2021, you do not have vaccine passports in the US, and kids went back to school earlier than they might have done. Our Election Integrity bill, which you all shared, has cosponsors in Wyoming, was introduced and defeated in Maine (but a successor has been tapped to re-introduce it in the Fall), and three other states, Michigan, Alabama and North Dakota, have citizens and legislators acting to push it forward. The Pfizer Papers comes out in May. The manuscript, which Amy Kelly and I edited, is 500 pages long. We edited 96 reports from the WarRoom/DailyClout Pfizer Documents Research Team, who in turn had reviewed 450,000 pages of internal Pfizer documents. They revealed the greatest crime against humanity in history in exhaustive detail, affecting people and governments worldwide. Their work is cited or used without citation by dozens of other freedom advocates, and legislators. And booster uptake is now down to 4%; Pfizer’s profits ground to pre-2016 levels. We saved, together, with your help, what may turn out to be millions of lives and countless unborn babies. But to continue, I need your help; seriously; now just now but into the future. If you can afford, it, and if the above is meaningful to you at all, do please upgrade your subscription from free to paid. The war is here, and you need warriors fighting for you, who are not barefoot in the snow, but who have warm clothing, and weapons, and ammunition. https://naomiwolf.substack.com/p/what-a-war-requires
    1 Comments 0 Shares 15103 Views
  • Chimaeras and interspecies hybrids; the sinister agenda hiding behind covid
    Rhoda WilsonMarch 20, 2024
    There is something that has quietly slipped through the din of the murderously phoney episode called covid-19, Dr. Mathew Maavak writes. “If the covid-19 vaccines were ‘experimental gene therapies’, what other genetic experimentations continue unhindered out there?” he asks.

    In May 2020, Dr. Maavak wrote an article about how SARS-CoV-2 was not germinated in a vacuum. The Wuhan Institute of Virology conducted research with alarming global parallels including the pursuit of superintelligence and the development of chimaeras, or interspecies hybrids.

    What he wrote in May 2020 is still relevant today, he says. So yesterday, Dr. Maavak reposted his now four-year-old article.

    Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…

    Coronavirus in a Time of Chimaeras and Beyond

    By Dr. Mathew Maavak

    In May 2020, just as the coronavirus made hourly headlines, I had suspected that the virus was part of a much more sinister agenda. What I wrote back then remains just as relevant today. Here it is.

    Genetically-Enhanced Competitiveness

    The Sars-Cov-2 virus, which allegedly causes covid-19, was not germinated in a vacuum. The type of research conducted at the Wuhan Institute of Virology had ominous analogues worldwide. These included the quest for super intelligence and the development of interspecies hybrids or chimaeras.

    What began as a scientific mission to remedy congenital defects has rapidly morphed into a global race to create designer babies, super soldiers and transhumans through the aid of biotechnology, artificial intelligence and/or machine-neuralinking. 21st century eugenics is tacitly justified by the need to boost “national competitiveness.”

    China leads the way here. In one revealing episode, genome sequencing giant BGI Shenzhen had procured and sequenced the DNA of more than 2,000 people – mostly Americans – with IQ scores of at least 160. According to Stephen Hsu, a theoretical physicist from Michigan State University and scientific adviser to BGI:

    An exceptional person gets you an order of magnitude more statistical power than if you took random people from the population …

    BGI Shenzhen intends to become a “bio-Google” that will collate the “world’s biological information and make it universally accessible and useful.” From 2012 onwards, it began collaborating with the Bill & Melinda Gates Foundation (“BMGF”). No surprises there.

    Scientific endeavours like these are based on the assumption that an assemblage of smart samples can help in the identification and transplantation of optimal bits of genetic material into future generations.

    Can a virus or vaccine perform this transplantation? Or will such agencies be used to cull the majority of the human population before a “genetic antidote” emerges to reverse their lethal effects? It will be too late for the vast majority of mankind by then. artificial selection, backed by artificial intelligence, may decide who gets this new booster. But is such a hypothetical scenario even realistic? There are too many imponderables here but viruses, nasal swabs and “vaccines” will surely deliver vital data for the “New Human Genome Project.”

    New Eugenics Zeitgeist

    The science of eugenics is not dissuaded by the nurture over nature debate, even after exhaustive studies had failed to establish genetic variants associated with intelligence. For example, a 2010 study led by Robert Plomin, a behavioural geneticist at King’s College London, had probed over 350,000 variations in single DNA letters across the genomes of 7,900 children but found no prized variant. Curiously, most of the smart samples procured by BGI Shenzhen were sourced from Plomin’s research activities.

    Periodic setbacks did not deter the proponents of “procreative beneficence” who argue that it is a human duty to augment the genetic codes of future generations. Failure to do so is couched in terms of “genetic neglect” and even child abuse. If this sounds eerily familiar, look no further than the worldview which once animated the Western world before the Nazis elevated it to a whole new level altogether.

    The eugenics zeitgeist has gripped China in a big way. Under its Maternal and Infant Health Care Law (1994), foetuses with potential hereditary diseases or deformities are recommended for abortion. At the rate Beijing is building its eugenics utopia, the definition of deformity may ultimately include a genetically pre-diagnosed average IQ.

    Instead of inciting public outrage, the law precipitated a headlong rush to select “intelligent” babies through methods like preimplantation genetic diagnosis (“PGD”). The idea behind PGD is to screen and identify the most promising embryos for implantation and birth. Combined with CRISPR gene-editing tools, next-generation Chinese citizens are expected to exhibit remarkably higher IQs – at least according to bioethicists who fret over a future marked by the “genetic haves” and “genetic have-nots.” China already has three CRISPR-edited babies whose current fate remains unknown.

    In the aftermath of the corona psychosis, the availability of “smart samples” would have increased exponentially and may dovetail nicely with the eugenics agenda of the Rockefeller Foundation and BMGF. Incidentally, Bill Gates grew up in a household that was heavily invested in population control and eugenics.

    Our smart societies may inevitably face the existential question of “live-lets” and “live-nots” down the line. The orchestrated rebellion towards selective extinction, if it occurs, has a tragicomical public face: An autistic Swede who parrots the “listen to the science” and “listen to the experts” mantra.

    How will future designer babies contribute to society? For one thing, we will be missing individuals like Beethoven (deaf); Albert Einstein (learning disability/late development); John Nash (schizophrenia); Andrea Boccelli (congenital glaucoma) and Vincent van Gogh (chronic depression/anxiety) and a host of others like them. A future Stephen Hawking (motor neurone disease) and Greta Thunberg (Asperger’s Syndrome – allegedly) will be genetically disqualified before birth.

    It is now inconvenient to consider intelligence as a result of peer interactions, human environment and ingenious reactions to adversity. (I personally define intelligence as an ability to nip the bullsh*t in its foetid bud).

    Mapping out the complex and sometimes unpredictable interplay between 100 trillion synaptic connections in a human brain may take centuries to accomplish but that does not deter the utopians of today.

    After all, genetic manipulation is the eugenic wormhole that promises to accelerate the emergence of a super society at warp speed. The late billionaire paedophile, Jeffrey Epstein, was a prominent proponent of this philosophy. Epstein intended to breed a “super race of humans with his DNA by impregnating women at his New Mexico ranch, genetic engineering and artificial intelligence.” Welcome to Lebensborn 2.0!

    Prominent scientists linked to Epstein’s transhumanist fantasies included “molecular engineer George Church; Murray Gell-Mann, the discoverer of the quark; the evolutionary biologist Stephen Jay Gould; the neurologist and author Oliver Sacks; and the theoretical physicist Frank Wilczek.” The late Stephen Hawking – who will ironically flunk the genetic pre-screenings of tomorrow – was another Epstein associate.

    Forget about Mars missions; major powers see eugenics as the next great frontier. Its hyper-materialistic focus is encapsulated by the following analogy from Russian scientist Denis Rebrikov:

    It currently costs about a million roubles (US$15,500 at that time) to genetically change an embryo – more than a lot of cars – but prices will fall with greater use … I can see the billboard now: “You Choose: a Hyundai Solaris or a Super-Child?”

    You are comparing a child, super or not, with a Hyundai? I mean a Hyundai, really? Sometimes, the road to hell is paved with good intentions but most of the time, it begins with a diabolically silly proposition.

    But why stop at children? From genetically engineered horses in Argentina that are supposedly faster, stronger and better jumpers to super-dogs in China that are comprehensively superior to the average mutt, the DNA of the entire natural world is being slated for a revolutionary redesign.

    Crouching Chimaeras, Hideous Hybrids

    The masters of our universe however cannot create future generations of superhumans without being adept at recombining genetic sequences across species. That is the logic guiding eugenicists. As a result, a slew of chimaeras or interspecies hybrids have been spawned with the aid of CRISPR technology. These include ghastly human-monkey hybrids, monkey-pig hybrids, human-rabbit hybrids and a host of other lab-manufactured monstrosities.

    Chimaeras are created when human embryonic stem cells are injected into embryos of other species. The goal, for the time being, is to induce growth of targeted human organs. Those facing terminal illnesses will no longer have to worry about long organ waiting lists. Chinese scientists have just transplanted a modified pig liver into a brain-dead human and it seems to have worked.

    A less controversial approach to human organ replacement is 3D bioprinting or its 4D bioprinting iteration. These techniques involve the “printing” of a replacement organ from the stem cells of a transplant recipient, thereby eliminating the odds of organ rejection.

    But why stop at replacement organs when we can have “replacement humans” altogether? Future generations must think like Einsteins, be as nimble as leopards and possess owl-like night visions. And, of course, be virus-resistant as well!

    The manipulation of the human genome is the new “grand response” to the venerable set of “grand challenges” for 2030 and beyond. China is the go-to place for such genetic tinkering as some of these undertakings are technically illegal in the West. And this is where the utility of covid-19 comes into the picture. It provides the perfect pretext to remove such ethical constraints. After all, “Disease X” is just waiting to escape from the belly of some bat or pangolin …

    Since 2014, the Wuhan Institute of Virology has been the recipient of a two-stage grant worth $7.2 million from the United States government for gain-of-function research into bat coronaviruses. According to a Newsweek report in April 2020:

    Many scientists have criticised gain of function research, which involves manipulating viruses in the lab to explore their potential for infecting humans because it creates a risk of starting a pandemic from accidental release.

    Such caution has not deterred a flurry of research into microbial gene manipulation. The Wuhan experiments may have either spawned the Sars-Cov-2 virus or it may have provided a fraudulent context for future tyrannical mandates.

    But to solely blame China for the coronavirus “pandemic” is a tad unfair. Just as China is the factory of the world for foreign corporations, it is also the genetic incubator for a variety of viruses and chimaeras for foreign governments and foundations. Even so, the human-pig chimaera was the creation of the Salk Institute in California. Research into the world’s first human-mouse hybrid was largely a Japanese affair. The Portuguese in the meantime had created a virus chimaera.

    The United Kingdom, on their end, had spawned a human-cow hybrid embryo in 2008 – perhaps in keeping with the bovine disposition of those glued to the BBC. It was in Britain where the game-changing Dolly the Sheep was cloned in 1996.

    The transition from sheep to sheeple may turn out to be a short 21st century Jurassic Park ride.

    Coincidences and Consequences

    Before the advent of gene-editing tools and supercomputing, it would have been impossible to create a viable chimaera. The Biotech-Industrial Complex and contact tracing-type panopticons constitute a new growth area for Tech Titans that were once facing bankruptcy.

    The dangers of genome editing were in fact included in the Worldwide Threat Assessment reports submitted to the United States Congress in 2016 and 2017. These risks were either omitted or glossed over in the 2018 and 2019 reports – just as such risks gravitated to the high impact-high likelihood quadrant.

    Is it a coincidence that the nations most affected by covid-19 – at least during the first two years of its alleged spread – were the very ones that had either promoted or encouraged a variety of genetic experimentations that are contrary to nature? If – and that is a big “if” – these nations succeed in their quest for “designer babies” and “superhumans,” the rest of mankind will be rendered redundant. Some mass extermination event may transpire under the guise of World War III, food shortages, Disease X or a combination thereof.


    If everything goes according to plan, however, there will be 500 million potential specimens left for The Great Reset. The Third World, whose leaders are being monetarily incentivised to focus on unattainable Sustainable Development Goals (“SDGs”), will be consigned to the ash heaps of history.

    It is quite ironic that a new generation of cerebrally deficient “thought leaders” and “experts” are being groomed to promote the demises of their societies and themselves.

    About the Author

    Mathew Maavak, with a PhD in Policy Studies, specialises in systems science, global risks, strategic foresight, geopolitics and governance. He is a Malaysian expert on risk foresight and governance.

    Dr. Maavak has published numerous op-eds on a variety of eclectic subjects for over 20 years – by ‘connecting the dots’ in a disjointed world. He is the author of a Substack page titled ‘The Eye Opener’ which you can subscribe to and follow HERE.



    https://expose-news.com/2024/03/20/chimaeras-and-interspecies-hybrids/
    Chimaeras and interspecies hybrids; the sinister agenda hiding behind covid Rhoda WilsonMarch 20, 2024 There is something that has quietly slipped through the din of the murderously phoney episode called covid-19, Dr. Mathew Maavak writes. “If the covid-19 vaccines were ‘experimental gene therapies’, what other genetic experimentations continue unhindered out there?” he asks. In May 2020, Dr. Maavak wrote an article about how SARS-CoV-2 was not germinated in a vacuum. The Wuhan Institute of Virology conducted research with alarming global parallels including the pursuit of superintelligence and the development of chimaeras, or interspecies hybrids. What he wrote in May 2020 is still relevant today, he says. So yesterday, Dr. Maavak reposted his now four-year-old article. Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… Coronavirus in a Time of Chimaeras and Beyond By Dr. Mathew Maavak In May 2020, just as the coronavirus made hourly headlines, I had suspected that the virus was part of a much more sinister agenda. What I wrote back then remains just as relevant today. Here it is. Genetically-Enhanced Competitiveness The Sars-Cov-2 virus, which allegedly causes covid-19, was not germinated in a vacuum. The type of research conducted at the Wuhan Institute of Virology had ominous analogues worldwide. These included the quest for super intelligence and the development of interspecies hybrids or chimaeras. What began as a scientific mission to remedy congenital defects has rapidly morphed into a global race to create designer babies, super soldiers and transhumans through the aid of biotechnology, artificial intelligence and/or machine-neuralinking. 21st century eugenics is tacitly justified by the need to boost “national competitiveness.” China leads the way here. In one revealing episode, genome sequencing giant BGI Shenzhen had procured and sequenced the DNA of more than 2,000 people – mostly Americans – with IQ scores of at least 160. According to Stephen Hsu, a theoretical physicist from Michigan State University and scientific adviser to BGI: An exceptional person gets you an order of magnitude more statistical power than if you took random people from the population … BGI Shenzhen intends to become a “bio-Google” that will collate the “world’s biological information and make it universally accessible and useful.” From 2012 onwards, it began collaborating with the Bill & Melinda Gates Foundation (“BMGF”). No surprises there. Scientific endeavours like these are based on the assumption that an assemblage of smart samples can help in the identification and transplantation of optimal bits of genetic material into future generations. Can a virus or vaccine perform this transplantation? Or will such agencies be used to cull the majority of the human population before a “genetic antidote” emerges to reverse their lethal effects? It will be too late for the vast majority of mankind by then. artificial selection, backed by artificial intelligence, may decide who gets this new booster. But is such a hypothetical scenario even realistic? There are too many imponderables here but viruses, nasal swabs and “vaccines” will surely deliver vital data for the “New Human Genome Project.” New Eugenics Zeitgeist The science of eugenics is not dissuaded by the nurture over nature debate, even after exhaustive studies had failed to establish genetic variants associated with intelligence. For example, a 2010 study led by Robert Plomin, a behavioural geneticist at King’s College London, had probed over 350,000 variations in single DNA letters across the genomes of 7,900 children but found no prized variant. Curiously, most of the smart samples procured by BGI Shenzhen were sourced from Plomin’s research activities. Periodic setbacks did not deter the proponents of “procreative beneficence” who argue that it is a human duty to augment the genetic codes of future generations. Failure to do so is couched in terms of “genetic neglect” and even child abuse. If this sounds eerily familiar, look no further than the worldview which once animated the Western world before the Nazis elevated it to a whole new level altogether. The eugenics zeitgeist has gripped China in a big way. Under its Maternal and Infant Health Care Law (1994), foetuses with potential hereditary diseases or deformities are recommended for abortion. At the rate Beijing is building its eugenics utopia, the definition of deformity may ultimately include a genetically pre-diagnosed average IQ. Instead of inciting public outrage, the law precipitated a headlong rush to select “intelligent” babies through methods like preimplantation genetic diagnosis (“PGD”). The idea behind PGD is to screen and identify the most promising embryos for implantation and birth. Combined with CRISPR gene-editing tools, next-generation Chinese citizens are expected to exhibit remarkably higher IQs – at least according to bioethicists who fret over a future marked by the “genetic haves” and “genetic have-nots.” China already has three CRISPR-edited babies whose current fate remains unknown. In the aftermath of the corona psychosis, the availability of “smart samples” would have increased exponentially and may dovetail nicely with the eugenics agenda of the Rockefeller Foundation and BMGF. Incidentally, Bill Gates grew up in a household that was heavily invested in population control and eugenics. Our smart societies may inevitably face the existential question of “live-lets” and “live-nots” down the line. The orchestrated rebellion towards selective extinction, if it occurs, has a tragicomical public face: An autistic Swede who parrots the “listen to the science” and “listen to the experts” mantra. How will future designer babies contribute to society? For one thing, we will be missing individuals like Beethoven (deaf); Albert Einstein (learning disability/late development); John Nash (schizophrenia); Andrea Boccelli (congenital glaucoma) and Vincent van Gogh (chronic depression/anxiety) and a host of others like them. A future Stephen Hawking (motor neurone disease) and Greta Thunberg (Asperger’s Syndrome – allegedly) will be genetically disqualified before birth. It is now inconvenient to consider intelligence as a result of peer interactions, human environment and ingenious reactions to adversity. (I personally define intelligence as an ability to nip the bullsh*t in its foetid bud). Mapping out the complex and sometimes unpredictable interplay between 100 trillion synaptic connections in a human brain may take centuries to accomplish but that does not deter the utopians of today. After all, genetic manipulation is the eugenic wormhole that promises to accelerate the emergence of a super society at warp speed. The late billionaire paedophile, Jeffrey Epstein, was a prominent proponent of this philosophy. Epstein intended to breed a “super race of humans with his DNA by impregnating women at his New Mexico ranch, genetic engineering and artificial intelligence.” Welcome to Lebensborn 2.0! Prominent scientists linked to Epstein’s transhumanist fantasies included “molecular engineer George Church; Murray Gell-Mann, the discoverer of the quark; the evolutionary biologist Stephen Jay Gould; the neurologist and author Oliver Sacks; and the theoretical physicist Frank Wilczek.” The late Stephen Hawking – who will ironically flunk the genetic pre-screenings of tomorrow – was another Epstein associate. Forget about Mars missions; major powers see eugenics as the next great frontier. Its hyper-materialistic focus is encapsulated by the following analogy from Russian scientist Denis Rebrikov: It currently costs about a million roubles (US$15,500 at that time) to genetically change an embryo – more than a lot of cars – but prices will fall with greater use … I can see the billboard now: “You Choose: a Hyundai Solaris or a Super-Child?” You are comparing a child, super or not, with a Hyundai? I mean a Hyundai, really? Sometimes, the road to hell is paved with good intentions but most of the time, it begins with a diabolically silly proposition. But why stop at children? From genetically engineered horses in Argentina that are supposedly faster, stronger and better jumpers to super-dogs in China that are comprehensively superior to the average mutt, the DNA of the entire natural world is being slated for a revolutionary redesign. Crouching Chimaeras, Hideous Hybrids The masters of our universe however cannot create future generations of superhumans without being adept at recombining genetic sequences across species. That is the logic guiding eugenicists. As a result, a slew of chimaeras or interspecies hybrids have been spawned with the aid of CRISPR technology. These include ghastly human-monkey hybrids, monkey-pig hybrids, human-rabbit hybrids and a host of other lab-manufactured monstrosities. Chimaeras are created when human embryonic stem cells are injected into embryos of other species. The goal, for the time being, is to induce growth of targeted human organs. Those facing terminal illnesses will no longer have to worry about long organ waiting lists. Chinese scientists have just transplanted a modified pig liver into a brain-dead human and it seems to have worked. A less controversial approach to human organ replacement is 3D bioprinting or its 4D bioprinting iteration. These techniques involve the “printing” of a replacement organ from the stem cells of a transplant recipient, thereby eliminating the odds of organ rejection. But why stop at replacement organs when we can have “replacement humans” altogether? Future generations must think like Einsteins, be as nimble as leopards and possess owl-like night visions. And, of course, be virus-resistant as well! The manipulation of the human genome is the new “grand response” to the venerable set of “grand challenges” for 2030 and beyond. China is the go-to place for such genetic tinkering as some of these undertakings are technically illegal in the West. And this is where the utility of covid-19 comes into the picture. It provides the perfect pretext to remove such ethical constraints. After all, “Disease X” is just waiting to escape from the belly of some bat or pangolin … Since 2014, the Wuhan Institute of Virology has been the recipient of a two-stage grant worth $7.2 million from the United States government for gain-of-function research into bat coronaviruses. According to a Newsweek report in April 2020: Many scientists have criticised gain of function research, which involves manipulating viruses in the lab to explore their potential for infecting humans because it creates a risk of starting a pandemic from accidental release. Such caution has not deterred a flurry of research into microbial gene manipulation. The Wuhan experiments may have either spawned the Sars-Cov-2 virus or it may have provided a fraudulent context for future tyrannical mandates. But to solely blame China for the coronavirus “pandemic” is a tad unfair. Just as China is the factory of the world for foreign corporations, it is also the genetic incubator for a variety of viruses and chimaeras for foreign governments and foundations. Even so, the human-pig chimaera was the creation of the Salk Institute in California. Research into the world’s first human-mouse hybrid was largely a Japanese affair. The Portuguese in the meantime had created a virus chimaera. The United Kingdom, on their end, had spawned a human-cow hybrid embryo in 2008 – perhaps in keeping with the bovine disposition of those glued to the BBC. It was in Britain where the game-changing Dolly the Sheep was cloned in 1996. The transition from sheep to sheeple may turn out to be a short 21st century Jurassic Park ride. Coincidences and Consequences Before the advent of gene-editing tools and supercomputing, it would have been impossible to create a viable chimaera. The Biotech-Industrial Complex and contact tracing-type panopticons constitute a new growth area for Tech Titans that were once facing bankruptcy. The dangers of genome editing were in fact included in the Worldwide Threat Assessment reports submitted to the United States Congress in 2016 and 2017. These risks were either omitted or glossed over in the 2018 and 2019 reports – just as such risks gravitated to the high impact-high likelihood quadrant. Is it a coincidence that the nations most affected by covid-19 – at least during the first two years of its alleged spread – were the very ones that had either promoted or encouraged a variety of genetic experimentations that are contrary to nature? If – and that is a big “if” – these nations succeed in their quest for “designer babies” and “superhumans,” the rest of mankind will be rendered redundant. Some mass extermination event may transpire under the guise of World War III, food shortages, Disease X or a combination thereof. If everything goes according to plan, however, there will be 500 million potential specimens left for The Great Reset. The Third World, whose leaders are being monetarily incentivised to focus on unattainable Sustainable Development Goals (“SDGs”), will be consigned to the ash heaps of history. It is quite ironic that a new generation of cerebrally deficient “thought leaders” and “experts” are being groomed to promote the demises of their societies and themselves. About the Author Mathew Maavak, with a PhD in Policy Studies, specialises in systems science, global risks, strategic foresight, geopolitics and governance. He is a Malaysian expert on risk foresight and governance. Dr. Maavak has published numerous op-eds on a variety of eclectic subjects for over 20 years – by ‘connecting the dots’ in a disjointed world. He is the author of a Substack page titled ‘The Eye Opener’ which you can subscribe to and follow HERE. https://expose-news.com/2024/03/20/chimaeras-and-interspecies-hybrids/
    EXPOSE-NEWS.COM
    Chimaeras and interspecies hybrids; the sinister agenda hiding behind covid
    There is something that has quietly slipped through the din of the murderously phoney episode called covid-19, Dr. Mathew Maavak writes. “If the covid-19 vaccines were ‘experimental gene therapies…
    1 Comments 0 Shares 15166 Views
  • Discovering an Azoran alternative in Ayurveda offers a holistic pathway for individuals navigating autoimmune conditions. Ayurveda, the ancient Indian system of medicine, presents a treasure trove of herbal remedies, dietary recommendations, and lifestyle adjustments aimed at restoring balance to the body and mind. In this insightful guide, we explore Ayurvedic perspectives on autoimmune disorders and unveil potent herbs such as Ashwagandha (Withania somnifera) and Guduchi (Tinospora cordifolia) that serve as alternatives to Azoran.

    For more info visit: https://www.planetayurveda.com/library/azathioprine-side-effects-and-safe-alternatives/
    Discovering an Azoran alternative in Ayurveda offers a holistic pathway for individuals navigating autoimmune conditions. Ayurveda, the ancient Indian system of medicine, presents a treasure trove of herbal remedies, dietary recommendations, and lifestyle adjustments aimed at restoring balance to the body and mind. In this insightful guide, we explore Ayurvedic perspectives on autoimmune disorders and unveil potent herbs such as Ashwagandha (Withania somnifera) and Guduchi (Tinospora cordifolia) that serve as alternatives to Azoran. For more info visit: https://www.planetayurveda.com/library/azathioprine-side-effects-and-safe-alternatives/
    WWW.PLANETAYURVEDA.COM
    Azathioprine Side Effects and Alternatives In Ayurveda
    Azathioprine (AZA) is an immunosuppressive agent which is associated with the conditions such as Atopic dermatitis, (ITP), and Psoriasis.
    0 Comments 0 Shares 2263 Views
  • Scientist claims ‘smoking gun’ evidence COVID-19 intentionally created by researchers in Chinese lab
    Ronny Reyes
    COVID-19 may have been created in a Chinese lab, a British professor told the UN Wednesday, with another expert claiming that evidence of the likelihood has reached “the level of a smoking gun.”

    Richard H. Ebright, a molecular biologist at Rutgers University, was quoted saying in a new Wall Street Journal article that the virus that killed millions around the world may actually have been manmade in China’s Wuhan Institute of Virology.

    He cited evidence found in a 2018 document from the lab that talked of making such a virus.

    Advertisement

    “[The document] elevates the evidence provided by the genome sequence from the level of noteworthy to the level of a smoking gun,” Ebright said in the piece by former New York Times editor Nicholas Wade.

    Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was man-made. 4
    Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was manmade. Rutgers New Brunswick
    The papers from the lab cited by Ebright contained drafts and notes regarding a grant proposal called Project DEFUSE, which sought to test engineering bat coronaviruses in a way that would make them more easily transmissible to humans.

    The proposal was ultimately rejected and denied funding by the US Defense Advanced Research Projects Agency, but Wade suggested that their work could have been carried out by researchers in Wuhan who had secured Chinese government funding.

    Advertisement

    “Viruses made according to the DEFUSE protocol could have been available by the time Covid-19 broke out, sometime between August and November 2019,” wrote Wade, a former science editor of the New York Times.

    Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. 4
    Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. AFP via Getty Images
    “This would account for the otherwise unexplained timing of the pandemic along with its place of origin.”

    Along with the research notes, Wade claimed the specific genetic structure of the coronavirus that allowed it to infect humans served as another strong indication of “the virus’s laboratory birth.”

    Advertisement

    “Whereas most viruses require repeated tries to switch from an animal host to people, SARS-CoV-2 infected humans out of the box, as if it had been preadapted while growing in the humanized mice called for in the DEFUSE protocol,” Wade wrote.

    While scientists continue to debate whether the coronavirus pandemic was a natural occurrence or manmade, Ebright believed there was credibility that the work proposed by the now-controversial EcoHealth Alliance led to the development COVID-19.

    Following the release of the 2018 documents — which were published by US Right to Know through a Freedom of Information Act request — Ebright said there was clearer evidence that the virus was manufactured in a lab, the Daily Telegraph reported.

    Advertisement

    The 2018 documents contained drafts and notes regarding Project DEFUSE and how to synthesize bat coronaviruses to make them more transmissible.

    The Wuhan Institute of Virology stands at the center of scrutiny over the origins of Covid-19. 4
    The Wuhan Institute of Virology stands at the center of scrutiny over the origins of COVID-19. AFP via Getty Images
    The researchers proposed introducing “appropriate human-specific cleavage sites” to the spike proteins of SARS-related viruses in the lab, the same method several biologists have said could have been used to synthesize the coronavirus that led to the pandemic.

    According to the documents, the researchers had planned to conduct a portion of the research at the Wuhan lab where they noted that safety conditions were not up to US standards, to the point where they claimed American scientists would “likely freak out.”

    Advertisement

    A spokesperson for EcoHealth Alliance said its research played no role in the start of the COVID-19 pandemic.

    “Documents representing incomplete or early drafts of the proposal have been acquired via the Freedom of Information Act and published along with allegations regarding their intent. These allegations are false, based on misunderstanding of edits and comments on the document, and based on misleading out-of-context quotations, and a lack of understanding of the process by which federal grants are awarded,” the spokesperson said.

    “Because the work was not selected for funding, any assertions about these details are by definition based on review of incomplete information and are extremely misleading.”

    Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London. 4
    Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, called on scientists to follow more rigorous safety standards. King College London
    Advertisement

    While COVID-19’s origins remain a mystery, Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, said the world needed to acknowledge that the possibility exists that the virus was synthesized.

    Speaking before the UN in New York on Wednesday, Lentzos presented the work of the Independent Task Force on Research with Pandemic Risks, which calls on scientists the world over to follow stricter regulations lest another worldwide breakout occur, the Telegraph reported.

    “We have to acknowledge the fact that the pandemic could have started from some research-related incident,” Lentzos said.

    Advertisement

    “Are we going to find that out? In my view, I think it’s very unlikely that we will. We need to do better in the future,” she added.

    “We are going to see more ambiguous events.”


    https://nypost.com/2024/02/29/world-news/scientists-may-have-started-the-covid-pandemic-article/


    https://telegra.ph/Scientist-claims-smoking-gun-evidence-COVID-19-intentionally-created-by-researchers-in-Chinese-lab-03-11
    Scientist claims ‘smoking gun’ evidence COVID-19 intentionally created by researchers in Chinese lab Ronny Reyes COVID-19 may have been created in a Chinese lab, a British professor told the UN Wednesday, with another expert claiming that evidence of the likelihood has reached “the level of a smoking gun.” Richard H. Ebright, a molecular biologist at Rutgers University, was quoted saying in a new Wall Street Journal article that the virus that killed millions around the world may actually have been manmade in China’s Wuhan Institute of Virology. He cited evidence found in a 2018 document from the lab that talked of making such a virus. Advertisement “[The document] elevates the evidence provided by the genome sequence from the level of noteworthy to the level of a smoking gun,” Ebright said in the piece by former New York Times editor Nicholas Wade. Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was man-made. 4 Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was manmade. Rutgers New Brunswick The papers from the lab cited by Ebright contained drafts and notes regarding a grant proposal called Project DEFUSE, which sought to test engineering bat coronaviruses in a way that would make them more easily transmissible to humans. The proposal was ultimately rejected and denied funding by the US Defense Advanced Research Projects Agency, but Wade suggested that their work could have been carried out by researchers in Wuhan who had secured Chinese government funding. Advertisement “Viruses made according to the DEFUSE protocol could have been available by the time Covid-19 broke out, sometime between August and November 2019,” wrote Wade, a former science editor of the New York Times. Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. 4 Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. AFP via Getty Images “This would account for the otherwise unexplained timing of the pandemic along with its place of origin.” Along with the research notes, Wade claimed the specific genetic structure of the coronavirus that allowed it to infect humans served as another strong indication of “the virus’s laboratory birth.” Advertisement “Whereas most viruses require repeated tries to switch from an animal host to people, SARS-CoV-2 infected humans out of the box, as if it had been preadapted while growing in the humanized mice called for in the DEFUSE protocol,” Wade wrote. While scientists continue to debate whether the coronavirus pandemic was a natural occurrence or manmade, Ebright believed there was credibility that the work proposed by the now-controversial EcoHealth Alliance led to the development COVID-19. Following the release of the 2018 documents — which were published by US Right to Know through a Freedom of Information Act request — Ebright said there was clearer evidence that the virus was manufactured in a lab, the Daily Telegraph reported. Advertisement The 2018 documents contained drafts and notes regarding Project DEFUSE and how to synthesize bat coronaviruses to make them more transmissible. The Wuhan Institute of Virology stands at the center of scrutiny over the origins of Covid-19. 4 The Wuhan Institute of Virology stands at the center of scrutiny over the origins of COVID-19. AFP via Getty Images The researchers proposed introducing “appropriate human-specific cleavage sites” to the spike proteins of SARS-related viruses in the lab, the same method several biologists have said could have been used to synthesize the coronavirus that led to the pandemic. According to the documents, the researchers had planned to conduct a portion of the research at the Wuhan lab where they noted that safety conditions were not up to US standards, to the point where they claimed American scientists would “likely freak out.” Advertisement A spokesperson for EcoHealth Alliance said its research played no role in the start of the COVID-19 pandemic. “Documents representing incomplete or early drafts of the proposal have been acquired via the Freedom of Information Act and published along with allegations regarding their intent. These allegations are false, based on misunderstanding of edits and comments on the document, and based on misleading out-of-context quotations, and a lack of understanding of the process by which federal grants are awarded,” the spokesperson said. “Because the work was not selected for funding, any assertions about these details are by definition based on review of incomplete information and are extremely misleading.” Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London. 4 Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, called on scientists to follow more rigorous safety standards. King College London Advertisement While COVID-19’s origins remain a mystery, Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, said the world needed to acknowledge that the possibility exists that the virus was synthesized. Speaking before the UN in New York on Wednesday, Lentzos presented the work of the Independent Task Force on Research with Pandemic Risks, which calls on scientists the world over to follow stricter regulations lest another worldwide breakout occur, the Telegraph reported. “We have to acknowledge the fact that the pandemic could have started from some research-related incident,” Lentzos said. Advertisement “Are we going to find that out? In my view, I think it’s very unlikely that we will. We need to do better in the future,” she added. “We are going to see more ambiguous events.” https://nypost.com/2024/02/29/world-news/scientists-may-have-started-the-covid-pandemic-article/ https://telegra.ph/Scientist-claims-smoking-gun-evidence-COVID-19-intentionally-created-by-researchers-in-Chinese-lab-03-11
    NYPOST.COM
    Scientist claims ‘smoking gun’ evidence COVID-19 intentionally created by researchers in Chinese lab
    Covid-19 may have been created by a “research-related incident,” a British professor told the UN Wednesday, with Richard H. Ebright, a molecular biologist at Rutgers University, claimin…
    Like
    1
    0 Comments 1 Shares 5377 Views
  • Judaism: Satanism, Sorcery and Black Magic | VT Foreign Policy
    February 23, 2024
    VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

    $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts
    Source: Embassy of Israel, Washington, D.C. and US Department of State.



    …by Jonas E. Alexis, Eric Gajewski, and Michael Hoffman

    Jonas E. Alexis: You have just published an article by Michael Hoffman, author of Judaism Discovered, and it almost certainly will ruffle people’s feathers because it goes into the dark world of Judaism, Cabbala and Freemasonry. E. Michael Jones has an entire chapter of this topic in his study The Jewish Revolutionary Spirit and Its Impact on World History.[1]

    According to Jones, Jewish revolutionaries were using secret societies such as Freemasonry and the Rosicrucian to bring down Western Civilization during the French Revolution. Voltaire himself was a Freemason and was indirectly aiding Judaism when he said: “Let the real Philosophers unite in a brotherhood like the Freemasons; let them assemble together and support each other, and let them be faithful to the association.”[2] Jones writes,

    “The theological foundation of the French Revolution becomes clear when Barruel’s exposition of Masonic ritual. The philosophes began their assault on the ancient regime by subverting morals, but the goal was always theological. Freemasonry’s attack on Christ was inspired by the Talmudic literature in the Cabala…Freemasonry is ultimately Judaizing.”[3]

    Is there a lot of Judaizing going on today?

    Eric Gajewski: This article and analysis by Mr Hoffman is timely. We must understand that from a Catholic’s perspective “Israel” or Zion was always a reference to the Catholic Church not some sort of “puppet state of Israel” created by those who truly hate Our Lord. Their “messiah” to come is not ours.

    Yet how many supposed Christians do you know are following this heresy? Certainly, the majority of “Christians” in America are. Now, we see in the news talk of a rebuilt third temple. You see many “Christians” getting excited because they think the second coming of Christ is coming. Ehh…wrong!

    Who is behind the New World Order? The answer becomes obvious after some basic study. We are moving out of a truly Catholic society right into the arms of the Antichrist himself. Let us recall the words of Rabbi Waton:

    “Judaism is communism, internationalism, the universal brotherhood of man, the emancipation of the working class and the human society. It is with these spiritual weapons that the Jews will conquer the world and the human race. The races and the nations will cheerfully submit to the spiritual power of Judaism, and all will become Jews….”

    Everybody should be able to see the evil principles in place and it should no longer surprise anyone at this point to see the further persecution of Catholicism/Christianity. It is time to draw a line in the sand.

    Michael Hoffman: The Kabbalah (“reception”), is a series of books of magic and mysticism. The canon has not been strictly defined although the rabbinic consensus names the Zohar as the most important volume. Another book, Sefer Yetzirah is a guide to black magic in Judaism.

    Zoharic studies in English have been advanced exponentially by the recent publication of Daniel Matt’s uncensored translation of all of the volumes traditionally associated with the Zohar.

    The descriptive term “Satanic” is overworked in this age of the Internet and “desktop” publishing. We do not propose to employ it casually or imprecisely. The Kabbalah is fundamentally Satanic in its theological orientation…

    The Kabbalah is attributed to the Rabbi Shimon ben Yoahi who wrote, “Even the best of the gentiles should all be killed.”

    Like the Talmud of Babylon, it is reputed to be derived form an Oral Law which God gave to Moses on Sinai in addition to the Written Law. In a cryptic passage from a book of the Kabbalah (Tikkunei Zohar 1:27b), buried within a double-entendre, is a reference to the Mishnah (first book of the Talmud) actually being “the burial place of Moses.” Furthermore, the rabbinic authors of the Mishnah admit to each other that their teachings and laws have “scant scriptural basis.”

    Judaics under Kabbalistic auspices are said to be under the dominion of the sitra ahra (“evil inclination”).

    SECRET MEANINGS, SEX CULT

    Kabbalistic exegesis of the Old Testament predicates a secret meaning that can be discerned by assigning each word of the Hebrew Bible a number through a process known as gematria, and then combining these numbers corresponding to letters, creating a new Bible unknown to the masses.

    The Kabbalah makes reference to the evil forces that will control Israel “in the secrecy of the steep,” when the spirits of the former zealots reincarnate on earth, forsaking their post-Second Temple exile to take up residence in Jerusalem yet again.[4]

    In Kabbalistic terms, “Evil forces attach themselves to holiness.”

    Patently, what is being called “holy” is not in accord with any Christian understanding of holiness, but rather in the pagan (Tantric) understanding that “defilement is a source of holiness.” That Jerusalem is the gateway to hell is celebrated in this mystical Kabbalistic sense, since it was known to and admitted by the rabbinate for centuries, that the evil forces are “most powerful in the Land of Israel, particularly in Jerusalem,” with the land’s “awesome powers” facilitating the process of demon worship and the resulting acquisition of material power on earth.[5]

    The Babylonian Talmud claims that the forbidden tree in the Garden from which Adam ate was a fig: “Rabbi Nehemiah holds that the tree of which Adam ate was the fig tree” (BT Berakoth 40a). The Kabbalah teaches that the leaves of this fig tree conveyed powers of sorcery and magic (Zohar 1:56b Bereshit).

    Consequently, in the rabbinic mind, the aprons worn by Adam and Eve, being made from the leaves of the fig tree, were garments that gave the wearers magical powers. These aprons made from fig leaves had the power to give the bearer the ability to enjoy “the fruits of the world-to-come” in the here-and-now. (BT Bava Metzia 114b). It is with this rabbinic understanding that Freemasons and Mormons wear these aprons in their own rituals.[6]

    The Zohar states that by black magic, Adam cut in half the divine unity of the god and goddess. Adam was formerly a giant, but after his sin his physical proportions were shrunk by God and “his erect stature diminished by one hundred cubits.” (Zohar 1:53b). In the fertile rabbinic imagination, most of the Book of Genesis, when taken literally, is misleading.

    In Zohar 1:36a Bereshit, an account is given of the temptation of Eve in Genesis 3: 4-6: “Eat from it and you will really be like Elohim, knowing good and evil.” After quoting this text, the Zohar reports that “Rabbi Yehudah said, This is not what the serpent said. For if he had said, ‘With this tree the Blessed Holy One created the world,’ it would have been a correct statement.

    What the serpent said was actually this: ‘The Blessed Holy One ate from this tree and then created the world…Eat from it and you will be creating worlds.””Zoharic Kabbalah…is centered on a blatantly erotic interpretation of the Godhead, dividing the functions of the sefirot into male and female sides. The Zohar includes multiple interpretations built around a concept of God’s ‘genitals.’

    Using a phrase in Isaiah, ‘behold the King in his beauty,’ (33:17) as its springboard, the Zohar interprets the word for yofi, ‘beauty’ as a euphemism for a divine member. Tikkuni Zohar explicitly claims the ‘divine image’ that God bestowed upon man (but not upon woman) was the penis (I: 62b, 94b). The Zohar also interprets a passage from Job, ‘In my flesh I see God,’ as a reference to the human penis being in ‘the image of God’…this supernal phallus is manifest in one or the other of two other sefirot, Tifferet…and Yesod…”[7]

    REDEMPTION THROUGH EVIL

    Judaism secretly teaches, as have the occult secret societies throughout the ages (in our time, Hindu Tantrism and the Ordo Templi Orientis or OTO), that the mystic can find redemption through a heroic willingness to do evil for the sake of a subsequent redemptive ascent to the highest spiritual good; immersion in the lowest of the low thus becomes a path to redemption: “…the concept of the descent of the Zaddiq, which is better known by the Hebrew phrase, Yeridah zorekh Aliyah, namely the descent for the sake of the ascent, the transgression for the sake of repentance…Much attention has been paid to this model because of its essential affinities with Zoharic and Lurianic Kabbalah…this model was a very important one in Hasidic thought…”[8]

    In other words, the rabbinic doctrine that evil can be redeemed by embracing it, was in circulation in early Hasidism until it threatened to expose the whole truth about the rabbinic religion, after which damage control was instituted through the familiar deception system of permissible dissimulation through dispensational revelation.

    In Hasidic Judaism’s first dispensation, the founding era of the Baal Shem Tov (early to mid-eighteenth century) and the disciples who came immediately in his wake, the grossest superstitions and the darkest dimensions of Babylonian Judaism were popularized among the Judaic masses, including the teaching that the “Jew” was to redeem the 288 “holy sparks” that exist in wicked thoughts (mahashavot zarot) and actions, by meditating upon them and implementing them, with the ostensible goal of “elevating” them.

    There was a sustained outcry, however, against this teaching from the rabbis of the non-Hasidic, “Mithnagdim” school, who complained bitterly that the Hasidim were “…popularizing mystical concepts that hitherto had zealously been kept concealed by the rabbis.” The complaint by the Mithnagdim has been represented to the outside world as a principled protest against excessive mysticism which “distorts” the austere Mosaic purity of rabbinic Judaism.

    Various forms of black magic (what Moshe Idel is pleased to call “the ancient Jewish mystical ascent as performed by the ‘descenders to the Merkavah”), superstition, goddess-worship, reincarnation and idolatry incontrovertibly comprise the under-publicized, formative core of Judaism’s oral traditions, and have exerted a profound influence on the rabbis since their sojourn in Babylon eighteen hundred years ago.[9]

    One of the oldest repositories of Babylonian magic in Judaism are the texts, Sifrei ha-Iyyun, the Sefer ha-Bahir and the Hilkoth Yesirah (also known as the Sefer Yetzirah), circa 200 A.D.; the earliest extant copy of the latter is the Genizah ms., tenth century. “…the practice associated with this school of thought is magical/theurgic, even including the attempt to make a golem.”[10]

    The “strand of earlier tradition is that of Merkavah mysticism. Merkavah designates a form of visionary mystical praxis that reaches back into the Hellenistic era but was still alive as late as tenth-century Babylonia…the old Merkavah and magical literature was preserved among the earliest Ashkenazic Jews…”[11]

    The best way for readers to acquaint themselves with the Kabbalah is to read the Zohar in the Matt translation. Two representative quotes from that volume are:

    “The evil impulse is good, and without the evil impulse, Israel cannot prevail in the world” (Zohar 161a); and: “Israel must make sacrifices to Satan so that he will leave Jerusalem unmolested.”

    Jonas E. Alexis: This “evil impulse” has never died out, and over the centuries has jumped around from place to place and movement to movement and has taken different forms and variations.

    It manifested itself briefly in fourteenth-century Spain when usury was used at an exorbitant rate, which ended up suppressing the peasants and provoking anti-Jewish reactions in the region. It sent shockwaves across much of Europe during the Hussite rebellion in the fifteenth century. It reached its pinnacle during the Peasant Revolt in the sixteenth century when judaizing Christians ended up smearing excrement on crucifixes and vandalizing and destroying churches and monasteries.

    In the seventeenth and eighteenth centuries, the revolutionary spirit produced false Jewish messiahs such as Shabbatai Zevi (1626-1676), who spearheaded the Sabbatean movement, and later produced staunch disciples and lesser known messiahs such as Barukhia Russo, Miguel Cardoso, Mordecai Mokia, Lobele Prossnitz, and Jacob Joseph Frank, compounding disaster on disaster.

    The revolutionary spirit swept Europe in the nineteenth century with the rise of Marxism, which was the ideological brainchild of Karl Marx and Moses Hess. In the nineteenth century, it showed itself in much of Europe and sections in America in the sex industry, which was largely a Jewish enterprise—an enterprise which gave rise to Hitler’s negative conception of the Jews.



    As we have seen earlier, this same “evil impulse” almost destroyed Berlin in the 1920s and 30s through moral corruption and degradation, but…

    [1] E. Michael Jones, The Jewish Revolutionary Spirit and Its Impact on World History (South Bend: Fidelity Press, 2008), chapter twelve, particularly pages 539-550.

    [2] Quoted in ibid., 546.

    [3] Ibid.

    [4] Zohar 184b.

    [5] Yehezkel Rabinowitz, Knesset Yehezkel (Bunden, 1913), p. 52. Moshe Halamish, “The Land of Israel innKabbalah” in A. Ravitsky (ed.), Eretz Yisrael, pp. 215-232. H.E. Shapira, Divrei Torah, 5:24; 6:25. Mendel Piekarz, Hasidut Polin. Jeremiah 32:31-32: “For this city (Jerusalem) hath been to me as a provocation of mine anger and of my fury from the day that they built it even unto this day; that I should remove it from before my face. Because of all the evil of the children of Israel and of the children of Judah, which they have done to provoke me to anger, they, their kings, their princes, their priests, and their prophets, and the men of Judah, and the inhabitants of Jerusalem.”

    [6] Cf. John L. Brooke, The Refiner’s Fire: The Making of Mormon Cosmology (Cambridge University Press, 1994) and Lance S. Owens, “Joseph Smith and Kabbalah: The Occult Connection,” in Dialogue: A Journal of Mormon Thought, Fall 1994. Smith enraged his brother Freemasons by incorporating secret Kabbalistic rituals in Mormon ceremonies. His occult church was seen as a growing rival to masonic power. In Carthage, Illinois in 1844, he was surrounded by a masonic mob (almost always described by establishment historians generically, as simply “a mob”), and out of awareness of its masonic personnel, Smith made the gesture of the masonic signal of distress, and shouted the code words, “Will no one help the widow’s son?” Faithful to their orders however, his erstwhile masonic-assassin brethren killed him on the spot. Cf. E. Cecil McGavin, Mormonism and Masonry (Bookcraft Publishers, 1956).

    [7] Rabbi Geoffrey W. Dennis, The Encyclopedia of Jewish Myth, Magic and Mysticism (2007), p. 199.

    [8] Idel, Hasidism Between Ecstasy and Magic, p. 103.

    [9] Ithamar Gruenwald, Israel Oriental Studies 1 (1971): pp. 132-177 and Temerin, vol. 7 (Jerusalem, 1972) pp.101-139. Gershom Scholem, Jewish Gnosticism, Merkabah Mysticism and Talmudic Tradition (Jewish Theological Seminary of America, 1965.

    [10] Daniel Matt, Zohar [Stanford, University 2004], v. 1. xxxvii].

    [11] Ibid., D. Matt, pp. xxxvi-xxxvii.


    ATTENTION READERS

    We See The World From All Sides and Want YOU To Be Fully Informed
    In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion.

    About VT - Policies & Disclosures - Comment Policy
    Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT.

    https://www.vtforeignpolicy.com/2024/02/judaism-satanism-sorcery-and-black-magic/
    Judaism: Satanism, Sorcery and Black Magic | VT Foreign Policy February 23, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. …by Jonas E. Alexis, Eric Gajewski, and Michael Hoffman Jonas E. Alexis: You have just published an article by Michael Hoffman, author of Judaism Discovered, and it almost certainly will ruffle people’s feathers because it goes into the dark world of Judaism, Cabbala and Freemasonry. E. Michael Jones has an entire chapter of this topic in his study The Jewish Revolutionary Spirit and Its Impact on World History.[1] According to Jones, Jewish revolutionaries were using secret societies such as Freemasonry and the Rosicrucian to bring down Western Civilization during the French Revolution. Voltaire himself was a Freemason and was indirectly aiding Judaism when he said: “Let the real Philosophers unite in a brotherhood like the Freemasons; let them assemble together and support each other, and let them be faithful to the association.”[2] Jones writes, “The theological foundation of the French Revolution becomes clear when Barruel’s exposition of Masonic ritual. The philosophes began their assault on the ancient regime by subverting morals, but the goal was always theological. Freemasonry’s attack on Christ was inspired by the Talmudic literature in the Cabala…Freemasonry is ultimately Judaizing.”[3] Is there a lot of Judaizing going on today? Eric Gajewski: This article and analysis by Mr Hoffman is timely. We must understand that from a Catholic’s perspective “Israel” or Zion was always a reference to the Catholic Church not some sort of “puppet state of Israel” created by those who truly hate Our Lord. Their “messiah” to come is not ours. Yet how many supposed Christians do you know are following this heresy? Certainly, the majority of “Christians” in America are. Now, we see in the news talk of a rebuilt third temple. You see many “Christians” getting excited because they think the second coming of Christ is coming. Ehh…wrong! Who is behind the New World Order? The answer becomes obvious after some basic study. We are moving out of a truly Catholic society right into the arms of the Antichrist himself. Let us recall the words of Rabbi Waton: “Judaism is communism, internationalism, the universal brotherhood of man, the emancipation of the working class and the human society. It is with these spiritual weapons that the Jews will conquer the world and the human race. The races and the nations will cheerfully submit to the spiritual power of Judaism, and all will become Jews….” Everybody should be able to see the evil principles in place and it should no longer surprise anyone at this point to see the further persecution of Catholicism/Christianity. It is time to draw a line in the sand. Michael Hoffman: The Kabbalah (“reception”), is a series of books of magic and mysticism. The canon has not been strictly defined although the rabbinic consensus names the Zohar as the most important volume. Another book, Sefer Yetzirah is a guide to black magic in Judaism. Zoharic studies in English have been advanced exponentially by the recent publication of Daniel Matt’s uncensored translation of all of the volumes traditionally associated with the Zohar. The descriptive term “Satanic” is overworked in this age of the Internet and “desktop” publishing. We do not propose to employ it casually or imprecisely. The Kabbalah is fundamentally Satanic in its theological orientation… The Kabbalah is attributed to the Rabbi Shimon ben Yoahi who wrote, “Even the best of the gentiles should all be killed.” Like the Talmud of Babylon, it is reputed to be derived form an Oral Law which God gave to Moses on Sinai in addition to the Written Law. In a cryptic passage from a book of the Kabbalah (Tikkunei Zohar 1:27b), buried within a double-entendre, is a reference to the Mishnah (first book of the Talmud) actually being “the burial place of Moses.” Furthermore, the rabbinic authors of the Mishnah admit to each other that their teachings and laws have “scant scriptural basis.” Judaics under Kabbalistic auspices are said to be under the dominion of the sitra ahra (“evil inclination”). SECRET MEANINGS, SEX CULT Kabbalistic exegesis of the Old Testament predicates a secret meaning that can be discerned by assigning each word of the Hebrew Bible a number through a process known as gematria, and then combining these numbers corresponding to letters, creating a new Bible unknown to the masses. The Kabbalah makes reference to the evil forces that will control Israel “in the secrecy of the steep,” when the spirits of the former zealots reincarnate on earth, forsaking their post-Second Temple exile to take up residence in Jerusalem yet again.[4] In Kabbalistic terms, “Evil forces attach themselves to holiness.” Patently, what is being called “holy” is not in accord with any Christian understanding of holiness, but rather in the pagan (Tantric) understanding that “defilement is a source of holiness.” That Jerusalem is the gateway to hell is celebrated in this mystical Kabbalistic sense, since it was known to and admitted by the rabbinate for centuries, that the evil forces are “most powerful in the Land of Israel, particularly in Jerusalem,” with the land’s “awesome powers” facilitating the process of demon worship and the resulting acquisition of material power on earth.[5] The Babylonian Talmud claims that the forbidden tree in the Garden from which Adam ate was a fig: “Rabbi Nehemiah holds that the tree of which Adam ate was the fig tree” (BT Berakoth 40a). The Kabbalah teaches that the leaves of this fig tree conveyed powers of sorcery and magic (Zohar 1:56b Bereshit). Consequently, in the rabbinic mind, the aprons worn by Adam and Eve, being made from the leaves of the fig tree, were garments that gave the wearers magical powers. These aprons made from fig leaves had the power to give the bearer the ability to enjoy “the fruits of the world-to-come” in the here-and-now. (BT Bava Metzia 114b). It is with this rabbinic understanding that Freemasons and Mormons wear these aprons in their own rituals.[6] The Zohar states that by black magic, Adam cut in half the divine unity of the god and goddess. Adam was formerly a giant, but after his sin his physical proportions were shrunk by God and “his erect stature diminished by one hundred cubits.” (Zohar 1:53b). In the fertile rabbinic imagination, most of the Book of Genesis, when taken literally, is misleading. In Zohar 1:36a Bereshit, an account is given of the temptation of Eve in Genesis 3: 4-6: “Eat from it and you will really be like Elohim, knowing good and evil.” After quoting this text, the Zohar reports that “Rabbi Yehudah said, This is not what the serpent said. For if he had said, ‘With this tree the Blessed Holy One created the world,’ it would have been a correct statement. What the serpent said was actually this: ‘The Blessed Holy One ate from this tree and then created the world…Eat from it and you will be creating worlds.””Zoharic Kabbalah…is centered on a blatantly erotic interpretation of the Godhead, dividing the functions of the sefirot into male and female sides. The Zohar includes multiple interpretations built around a concept of God’s ‘genitals.’ Using a phrase in Isaiah, ‘behold the King in his beauty,’ (33:17) as its springboard, the Zohar interprets the word for yofi, ‘beauty’ as a euphemism for a divine member. Tikkuni Zohar explicitly claims the ‘divine image’ that God bestowed upon man (but not upon woman) was the penis (I: 62b, 94b). The Zohar also interprets a passage from Job, ‘In my flesh I see God,’ as a reference to the human penis being in ‘the image of God’…this supernal phallus is manifest in one or the other of two other sefirot, Tifferet…and Yesod…”[7] REDEMPTION THROUGH EVIL Judaism secretly teaches, as have the occult secret societies throughout the ages (in our time, Hindu Tantrism and the Ordo Templi Orientis or OTO), that the mystic can find redemption through a heroic willingness to do evil for the sake of a subsequent redemptive ascent to the highest spiritual good; immersion in the lowest of the low thus becomes a path to redemption: “…the concept of the descent of the Zaddiq, which is better known by the Hebrew phrase, Yeridah zorekh Aliyah, namely the descent for the sake of the ascent, the transgression for the sake of repentance…Much attention has been paid to this model because of its essential affinities with Zoharic and Lurianic Kabbalah…this model was a very important one in Hasidic thought…”[8] In other words, the rabbinic doctrine that evil can be redeemed by embracing it, was in circulation in early Hasidism until it threatened to expose the whole truth about the rabbinic religion, after which damage control was instituted through the familiar deception system of permissible dissimulation through dispensational revelation. In Hasidic Judaism’s first dispensation, the founding era of the Baal Shem Tov (early to mid-eighteenth century) and the disciples who came immediately in his wake, the grossest superstitions and the darkest dimensions of Babylonian Judaism were popularized among the Judaic masses, including the teaching that the “Jew” was to redeem the 288 “holy sparks” that exist in wicked thoughts (mahashavot zarot) and actions, by meditating upon them and implementing them, with the ostensible goal of “elevating” them. There was a sustained outcry, however, against this teaching from the rabbis of the non-Hasidic, “Mithnagdim” school, who complained bitterly that the Hasidim were “…popularizing mystical concepts that hitherto had zealously been kept concealed by the rabbis.” The complaint by the Mithnagdim has been represented to the outside world as a principled protest against excessive mysticism which “distorts” the austere Mosaic purity of rabbinic Judaism. Various forms of black magic (what Moshe Idel is pleased to call “the ancient Jewish mystical ascent as performed by the ‘descenders to the Merkavah”), superstition, goddess-worship, reincarnation and idolatry incontrovertibly comprise the under-publicized, formative core of Judaism’s oral traditions, and have exerted a profound influence on the rabbis since their sojourn in Babylon eighteen hundred years ago.[9] One of the oldest repositories of Babylonian magic in Judaism are the texts, Sifrei ha-Iyyun, the Sefer ha-Bahir and the Hilkoth Yesirah (also known as the Sefer Yetzirah), circa 200 A.D.; the earliest extant copy of the latter is the Genizah ms., tenth century. “…the practice associated with this school of thought is magical/theurgic, even including the attempt to make a golem.”[10] The “strand of earlier tradition is that of Merkavah mysticism. Merkavah designates a form of visionary mystical praxis that reaches back into the Hellenistic era but was still alive as late as tenth-century Babylonia…the old Merkavah and magical literature was preserved among the earliest Ashkenazic Jews…”[11] The best way for readers to acquaint themselves with the Kabbalah is to read the Zohar in the Matt translation. Two representative quotes from that volume are: “The evil impulse is good, and without the evil impulse, Israel cannot prevail in the world” (Zohar 161a); and: “Israel must make sacrifices to Satan so that he will leave Jerusalem unmolested.” Jonas E. Alexis: This “evil impulse” has never died out, and over the centuries has jumped around from place to place and movement to movement and has taken different forms and variations. It manifested itself briefly in fourteenth-century Spain when usury was used at an exorbitant rate, which ended up suppressing the peasants and provoking anti-Jewish reactions in the region. It sent shockwaves across much of Europe during the Hussite rebellion in the fifteenth century. It reached its pinnacle during the Peasant Revolt in the sixteenth century when judaizing Christians ended up smearing excrement on crucifixes and vandalizing and destroying churches and monasteries. In the seventeenth and eighteenth centuries, the revolutionary spirit produced false Jewish messiahs such as Shabbatai Zevi (1626-1676), who spearheaded the Sabbatean movement, and later produced staunch disciples and lesser known messiahs such as Barukhia Russo, Miguel Cardoso, Mordecai Mokia, Lobele Prossnitz, and Jacob Joseph Frank, compounding disaster on disaster. The revolutionary spirit swept Europe in the nineteenth century with the rise of Marxism, which was the ideological brainchild of Karl Marx and Moses Hess. In the nineteenth century, it showed itself in much of Europe and sections in America in the sex industry, which was largely a Jewish enterprise—an enterprise which gave rise to Hitler’s negative conception of the Jews. As we have seen earlier, this same “evil impulse” almost destroyed Berlin in the 1920s and 30s through moral corruption and degradation, but… [1] E. Michael Jones, The Jewish Revolutionary Spirit and Its Impact on World History (South Bend: Fidelity Press, 2008), chapter twelve, particularly pages 539-550. [2] Quoted in ibid., 546. [3] Ibid. [4] Zohar 184b. [5] Yehezkel Rabinowitz, Knesset Yehezkel (Bunden, 1913), p. 52. Moshe Halamish, “The Land of Israel innKabbalah” in A. Ravitsky (ed.), Eretz Yisrael, pp. 215-232. H.E. Shapira, Divrei Torah, 5:24; 6:25. Mendel Piekarz, Hasidut Polin. Jeremiah 32:31-32: “For this city (Jerusalem) hath been to me as a provocation of mine anger and of my fury from the day that they built it even unto this day; that I should remove it from before my face. Because of all the evil of the children of Israel and of the children of Judah, which they have done to provoke me to anger, they, their kings, their princes, their priests, and their prophets, and the men of Judah, and the inhabitants of Jerusalem.” [6] Cf. John L. Brooke, The Refiner’s Fire: The Making of Mormon Cosmology (Cambridge University Press, 1994) and Lance S. Owens, “Joseph Smith and Kabbalah: The Occult Connection,” in Dialogue: A Journal of Mormon Thought, Fall 1994. Smith enraged his brother Freemasons by incorporating secret Kabbalistic rituals in Mormon ceremonies. His occult church was seen as a growing rival to masonic power. In Carthage, Illinois in 1844, he was surrounded by a masonic mob (almost always described by establishment historians generically, as simply “a mob”), and out of awareness of its masonic personnel, Smith made the gesture of the masonic signal of distress, and shouted the code words, “Will no one help the widow’s son?” Faithful to their orders however, his erstwhile masonic-assassin brethren killed him on the spot. Cf. E. Cecil McGavin, Mormonism and Masonry (Bookcraft Publishers, 1956). [7] Rabbi Geoffrey W. Dennis, The Encyclopedia of Jewish Myth, Magic and Mysticism (2007), p. 199. [8] Idel, Hasidism Between Ecstasy and Magic, p. 103. [9] Ithamar Gruenwald, Israel Oriental Studies 1 (1971): pp. 132-177 and Temerin, vol. 7 (Jerusalem, 1972) pp.101-139. Gershom Scholem, Jewish Gnosticism, Merkabah Mysticism and Talmudic Tradition (Jewish Theological Seminary of America, 1965. [10] Daniel Matt, Zohar [Stanford, University 2004], v. 1. xxxvii]. [11] Ibid., D. Matt, pp. xxxvi-xxxvii. ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/02/judaism-satanism-sorcery-and-black-magic/
    WWW.VTFOREIGNPOLICY.COM
    Judaism: Satanism, Sorcery and Black Magic
    …by Jonas E. Alexis, Eric Gajewski, and Michael Hoffman Jonas E. Alexis: You have just published an article by Michael Hoffman, author of Judaism Discovered, and it almost certainly will ruffle people’s feathers because it goes into the dark world of Judaism, Cabbala and Freemasonry. E. Michael Jones has an entire chapter of...
    0 Comments 0 Shares 22594 Views
  • CDC’s Own Scientists Found Masks Ineffective for Covid-19 but Recommended Them Anyway
    Officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness

    World Council for Health
    This article was originally published by The Defender — Children’s Health Defense’s News & Views Website.

    cdc masks ineffective covid feature
    The Centers for Disease Control and Prevention’s (CDC) own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by independent journalist Paul D. Thacker.

    The investigation, published this week in two parts on The Disinformation Chronicle, details how CDC leadership openly questioned the findings of CDC scientists’ studies contradicting the agency’s public messaging about mask effectiveness.

    During the pandemic, mask advocates “shifted goalposts and demanded N95 respirators,” Thacker said, claiming they perform better than surgical masks at stopping the virus.

    If this content is important to you, share it!

    Share

    However, Thacker said CDC scientists found no difference between N95 and surgical masks in the ability to stop the spread of respiratory viruses. The findings of the CDC studies are consistent with other peer-reviewed studies on the efficacy of masks in preventing COVID-19, according to Thacker.

    “But the CDC responded by saying people can’t say that,” Thacker told The Defender.

    To shut down the controversy, the CDC, in its Jan. 23 post on preventing the transmission of pathogens in healthcare settings, warned researchers that to suggest facemasks and respirators are the same “is not scientifically correct,” Thacker wrote.

    CDC ignores own studies questioning N95, mask effectiveness

    According to Thacker, CDC guidance for controlling the spread of infections had not been updated since 2007. This prompted the CDC, in 2022, to select “a bunch of science experts,” and ask them “to update the agency’s scientific guidance to hospitals on how to control infections.”

    In November 2023, the experts produced an 80-page systematic review and meta-analysis, examining whether N95 respirators were more effective than surgical masks. The review found that while N95 respirators are better at filtering particles, the finding that they are more effective at stopping viruses “has been less conclusive.”

    The systematic review also examined the “effectiveness” of N95 respirators and surgical masks “under ‘real world’” conditions and found “no difference” between the two.

    The review also found numerous symptoms reported by N95 mask users, including: “difficulty breathing, headaches, and dizziness; skin barrier damage and itching; fatigue; and difficulty talking.”

    According to Thacker, the CDC is not pleased with these findings, suggesting in its recent update that its own scientists were wrong.

    “Although masks can provide some level of filtration, the level of filtration is not comparable to NIOSH Approved respirators,” the CDC said.

    The post also stated, “The COVID-19 pandemic has forever changed the approach we take in healthcare settings to protect healthcare personnel, patients, and others from transmission of respiratory infections.”

    More evidence contradicting the CDC’s public position came at a June 2023 CDC meeting in Atlanta, when Erin Stone, MPH, a public health analyst in the agency’s Office of Guidelines and Evidence Review, presented the findings of a meta-analysis on the effectiveness of N95 respirators and surgical masks.

    According to Stone, the data “suggests no difference” in their effectiveness.

    Yet, in November 2023 testimony before the U.S. House of Representatives’ Energy and Commerce Committee, CDC Director Mandy Cohen sidestepped questions regarding mask effectiveness and refused to deny she would reinstate mask mandates for children.

    According to Thacker, in December 2023, just six days after Cohen’s testimony, The BMJ’s Archives of Disease in Childhood journal published a study finding that “mask recommendations for children are not supported by scientific evidence.”

    “Recommending child masking does not meet the accepted practice of promulgating only medical interventions where benefits clearly outweigh harms,” the study authors noted.

    Thacker: CDC guidance based on politics, not science

    Thacker said the CDC contradicted its own findings on mask efficacy even in the early stages of the COVID-19 pandemic.

    “Soon after the pandemic started, the CDC began promoting masks to stop the spread of COVID,” Thacker wrote. “And it did so despite CDC publishing a May 2020 policy study in their own journal, ‘Emerging Infectious Diseases,’ that did not find a ‘substantial effect’ for masks in stopping the transmission of respiratory viruses.”


    twitter.com/CDCgov/status/1378462317109731334
    That same month, the CDC began publicly promoting N95 respirators as a more effective means of controlling the spread of COVID-19.

    However, on its webpage promoting the superiority of N95 respirators, the CDC admitted “there’s not a whole lot of evidence that N95 respirators do in fact work better than masks at stopping viruses,” Thacker wrote.

    “Laboratory studies have demonstrated that FFRs [filtering facepiece respirators] provide greater protection against aerosols compared with surgical masks … however, the results of clinical studies have been inconclusive,” the CDC wrote, citing a 2019 study in JAMA comparing N95 respirators to masks.

    “Among outpatient health care personnel, N95 respirators vs medical masks as worn by participants in this trial resulted in no significant difference in the incidence of laboratory-confirmed influenza,” the JAMA study noted.


    twitter.com/CDCgov/status/1256655451195715585
    According to Thacker, the results of these studies confirm the widely accepted pre-COVID-19 scientific consensus on the ineffectiveness of masks of any kind in stopping the spread of viruses. Thacker cited statements the World Health Organization made in 2019 and the CDC’s guidance on virus control.

    In a 2020 appearance on CBS’ “60 Minutes,” Dr. Anthony Fauci said that while a mask might “block a droplet” and “make people feel a little better,” it does not provide “the perfect protection that people think it is.”



    According to Thacker, “For some reason, a ‘masks work’ political movement began to grow,” despite Fauci’s statements and the findings of these studies.

    “I’m not really sure what happened or what we do next,” Thacker wrote. “But something weird took place in America where liberal elites began messaging among themselves ‘masks work.’ They then grew this into a crusade.”

    The movement was effective in getting the CDC on board with issuing mask guidance, Thacker said.

    Four years after the onset of the pandemic, the CDC now openly cheerleads for masks, despite research the agency published showing that masks don’t really protect people from catching viruses, he said.

    “And this is why the experts advising the CDC are getting all this pushback: they didn’t tell the CDC what the CDC wanted to hear,” Thacker wrote.

    Harvey Risch, M.D., Ph.D., professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Disinformation Chronicle the CDC “has succumbed to political influences.”

    Risch said:

    “It made policies for school closures in order to please the teachers’ union. Its charitable organization allows pharma to feed it hundreds of millions of dollars that would be illegal to go directly to the agency, and this gives pharma major influence on CDC policies.”

    According to Thacker, the CDC has continued to double down on guidance promoting mask efficacy. A Jan. 23 letter the agency sent to its own advisers appears to encourage them to add more mask guidance to the agency’s new guidelines for the spread of pathogens, based on the conclusion that N95 respirators are effective.

    “Too much science is forcing CDC to request a science do over,” Thacker wrote, referring to the CDC’s Jan. 23 post, which states that its new recommendations should not “be misread to suggest equivalency between facemasks and NIOSH Approved respirators, which is not scientifically correct nor the intent of the draft language.”

    Thacker said his investigation shows that “in their guidance to the CDC, experts do recommend masks as part of what they call ‘transmission-based guidance’ which the CDC defines as a second tier of infection control.” However, the CDC’s own guidance also finds that masks are effective only for “source control” — preventing an already infected person from infecting others.

    “But this isn’t what the CDC wants,” Thacker wrote. “They want the experts to write guidelines that recommend healthy people wear masks, even though research shows masks won’t really stop healthy people from getting sick.”

    “The CDC has caught the ‘masks work’ political wave and is now demanding that independent experts conform to their preferred mask dictates,” he added.

    In doing so, the CDC is rejecting science it doesn’t like, including several other non-CDC studies that have questioned mask effectiveness.

    A study published in Annals of Internal Medicine in November 2022 found no difference between N95 respirators and surgical masks in stopping the spread of COVID-19. These findings were mirrored in a January 2023 Cochrane meta-analysis on mask effectiveness.

    According to the Cochrane report, “The use of a N95/P2 respirators compared to medical/surgical masks probably makes little or no difference for the objective and more precise outcome of laboratory‐confirmed influenza infection.”

    A May 2023 study published in Ecotoxicology and Environmental Safety suggests N95 respirators may expose wearers to dangerous levels of toxic compounds linked to seizures and cancer.

    A September 2023 meta-analysis published in Clinical Research Study examined mask studies published since 2019 in the CDC’s Morbidity and Mortality Weekly Report (MMWR).

    According to the findings of the meta-analysis:

    “MMWR publications pertaining to masks drew positive conclusions about mask effectiveness >75% of the time despite only 30% testing masks and <15% having statistically significant results. No studies were randomized, yet over half drew causal conclusions.

    “The level of evidence generated was low and the conclusions were most often unsupported by the data. Our findings raise concern about the reliability of the journal for informing health policy.”

    Real-world examples also call into question narratives regarding mask efficacy.

    Sweden, for instance, did not mandate or recommend masks for the general public during the first wave of the COVID-19 pandemic, and only did so in certain situations in the later stages of the pandemic, according to The Conversation. Yet, its total excess deaths during the first two years of the pandemic were among the lowest in Europe.”

    In 2020, Swedish state epidemiologist Anders Tegnell said, “We see no point in wearing a face mask in Sweden, not even on public transport,” adding there were “at least three heavyweight reports … which all state that the scientific evidence is weak.”

    A Swedish government commission noted low levels of excess mortality in 2020 and 2021 and said that, at most, masks should have been “recommended.”

    Soon after the report was released, a Feb. 25, 2022, Boston Herald op-ed stated that Sweden “got it right.”

    “I don’t understand what is driving the ‘masks work’ political movement,” Thacker told The Defender. “There were plenty of stories written pointing out that there isn’t much scientific evidence that masks stop respiratory virus spread.”

    “Maybe people were just scared and wanted to believe masks provide protection?” he said.

    Thacker also cited the historical precedent of the Spanish Flu epidemic in 1918, when the Red Cross campaigned for masks all across America.

    “California’s state board of health ran a study comparing towns that had mask mandates against those that did not. They found that there was no difference and published the study in the American Journal of Public Health in 1920,” Thacker said.

    “Maybe these mask campaigners need to read a little history,” he added.

    Thacker is now calling on whistleblowers inside the CDC to contact him “to discuss what is going on inside the agency.”

    “I’m talking to CDC people and hope to learn what is going on inside the agency. I plan to write more on this,” Thacker told The Defender.

    “CDC Director Mandy Cohen wants to restore trust in the agency, but that won’t happen if she keeps putting politics ahead of scientific evidence,” he said.

    If this content is important to you, share it with your network!

    Share

    This article was written by Michael Nevradakis, Ph.D. and originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.


    If you find value in this Substack and have the means, please consider making a contribution to support the World Council for Health. Thank you.

    Upgrade to Paid Subscription

    Refer a friend

    Donate Subscriptions

    Give Direct to WCH

    https://worldcouncilforhealth.substack.com/p/cdcs-own-scientists-found-masks-ineffective

    https://donshafi911.blogspot.com/2024/02/cdcs-own-scientists-found-masks_16.html
    CDC’s Own Scientists Found Masks Ineffective for Covid-19 but Recommended Them Anyway Officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness World Council for Health This article was originally published by The Defender — Children’s Health Defense’s News & Views Website. cdc masks ineffective covid feature The Centers for Disease Control and Prevention’s (CDC) own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by independent journalist Paul D. Thacker. The investigation, published this week in two parts on The Disinformation Chronicle, details how CDC leadership openly questioned the findings of CDC scientists’ studies contradicting the agency’s public messaging about mask effectiveness. During the pandemic, mask advocates “shifted goalposts and demanded N95 respirators,” Thacker said, claiming they perform better than surgical masks at stopping the virus. If this content is important to you, share it! Share However, Thacker said CDC scientists found no difference between N95 and surgical masks in the ability to stop the spread of respiratory viruses. The findings of the CDC studies are consistent with other peer-reviewed studies on the efficacy of masks in preventing COVID-19, according to Thacker. “But the CDC responded by saying people can’t say that,” Thacker told The Defender. To shut down the controversy, the CDC, in its Jan. 23 post on preventing the transmission of pathogens in healthcare settings, warned researchers that to suggest facemasks and respirators are the same “is not scientifically correct,” Thacker wrote. CDC ignores own studies questioning N95, mask effectiveness According to Thacker, CDC guidance for controlling the spread of infections had not been updated since 2007. This prompted the CDC, in 2022, to select “a bunch of science experts,” and ask them “to update the agency’s scientific guidance to hospitals on how to control infections.” In November 2023, the experts produced an 80-page systematic review and meta-analysis, examining whether N95 respirators were more effective than surgical masks. The review found that while N95 respirators are better at filtering particles, the finding that they are more effective at stopping viruses “has been less conclusive.” The systematic review also examined the “effectiveness” of N95 respirators and surgical masks “under ‘real world’” conditions and found “no difference” between the two. The review also found numerous symptoms reported by N95 mask users, including: “difficulty breathing, headaches, and dizziness; skin barrier damage and itching; fatigue; and difficulty talking.” According to Thacker, the CDC is not pleased with these findings, suggesting in its recent update that its own scientists were wrong. “Although masks can provide some level of filtration, the level of filtration is not comparable to NIOSH Approved respirators,” the CDC said. The post also stated, “The COVID-19 pandemic has forever changed the approach we take in healthcare settings to protect healthcare personnel, patients, and others from transmission of respiratory infections.” More evidence contradicting the CDC’s public position came at a June 2023 CDC meeting in Atlanta, when Erin Stone, MPH, a public health analyst in the agency’s Office of Guidelines and Evidence Review, presented the findings of a meta-analysis on the effectiveness of N95 respirators and surgical masks. According to Stone, the data “suggests no difference” in their effectiveness. Yet, in November 2023 testimony before the U.S. House of Representatives’ Energy and Commerce Committee, CDC Director Mandy Cohen sidestepped questions regarding mask effectiveness and refused to deny she would reinstate mask mandates for children. According to Thacker, in December 2023, just six days after Cohen’s testimony, The BMJ’s Archives of Disease in Childhood journal published a study finding that “mask recommendations for children are not supported by scientific evidence.” “Recommending child masking does not meet the accepted practice of promulgating only medical interventions where benefits clearly outweigh harms,” the study authors noted. Thacker: CDC guidance based on politics, not science Thacker said the CDC contradicted its own findings on mask efficacy even in the early stages of the COVID-19 pandemic. “Soon after the pandemic started, the CDC began promoting masks to stop the spread of COVID,” Thacker wrote. “And it did so despite CDC publishing a May 2020 policy study in their own journal, ‘Emerging Infectious Diseases,’ that did not find a ‘substantial effect’ for masks in stopping the transmission of respiratory viruses.” twitter.com/CDCgov/status/1378462317109731334 That same month, the CDC began publicly promoting N95 respirators as a more effective means of controlling the spread of COVID-19. However, on its webpage promoting the superiority of N95 respirators, the CDC admitted “there’s not a whole lot of evidence that N95 respirators do in fact work better than masks at stopping viruses,” Thacker wrote. “Laboratory studies have demonstrated that FFRs [filtering facepiece respirators] provide greater protection against aerosols compared with surgical masks … however, the results of clinical studies have been inconclusive,” the CDC wrote, citing a 2019 study in JAMA comparing N95 respirators to masks. “Among outpatient health care personnel, N95 respirators vs medical masks as worn by participants in this trial resulted in no significant difference in the incidence of laboratory-confirmed influenza,” the JAMA study noted. twitter.com/CDCgov/status/1256655451195715585 According to Thacker, the results of these studies confirm the widely accepted pre-COVID-19 scientific consensus on the ineffectiveness of masks of any kind in stopping the spread of viruses. Thacker cited statements the World Health Organization made in 2019 and the CDC’s guidance on virus control. In a 2020 appearance on CBS’ “60 Minutes,” Dr. Anthony Fauci said that while a mask might “block a droplet” and “make people feel a little better,” it does not provide “the perfect protection that people think it is.” According to Thacker, “For some reason, a ‘masks work’ political movement began to grow,” despite Fauci’s statements and the findings of these studies. “I’m not really sure what happened or what we do next,” Thacker wrote. “But something weird took place in America where liberal elites began messaging among themselves ‘masks work.’ They then grew this into a crusade.” The movement was effective in getting the CDC on board with issuing mask guidance, Thacker said. Four years after the onset of the pandemic, the CDC now openly cheerleads for masks, despite research the agency published showing that masks don’t really protect people from catching viruses, he said. “And this is why the experts advising the CDC are getting all this pushback: they didn’t tell the CDC what the CDC wanted to hear,” Thacker wrote. Harvey Risch, M.D., Ph.D., professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Disinformation Chronicle the CDC “has succumbed to political influences.” Risch said: “It made policies for school closures in order to please the teachers’ union. Its charitable organization allows pharma to feed it hundreds of millions of dollars that would be illegal to go directly to the agency, and this gives pharma major influence on CDC policies.” According to Thacker, the CDC has continued to double down on guidance promoting mask efficacy. A Jan. 23 letter the agency sent to its own advisers appears to encourage them to add more mask guidance to the agency’s new guidelines for the spread of pathogens, based on the conclusion that N95 respirators are effective. “Too much science is forcing CDC to request a science do over,” Thacker wrote, referring to the CDC’s Jan. 23 post, which states that its new recommendations should not “be misread to suggest equivalency between facemasks and NIOSH Approved respirators, which is not scientifically correct nor the intent of the draft language.” Thacker said his investigation shows that “in their guidance to the CDC, experts do recommend masks as part of what they call ‘transmission-based guidance’ which the CDC defines as a second tier of infection control.” However, the CDC’s own guidance also finds that masks are effective only for “source control” — preventing an already infected person from infecting others. “But this isn’t what the CDC wants,” Thacker wrote. “They want the experts to write guidelines that recommend healthy people wear masks, even though research shows masks won’t really stop healthy people from getting sick.” “The CDC has caught the ‘masks work’ political wave and is now demanding that independent experts conform to their preferred mask dictates,” he added. In doing so, the CDC is rejecting science it doesn’t like, including several other non-CDC studies that have questioned mask effectiveness. A study published in Annals of Internal Medicine in November 2022 found no difference between N95 respirators and surgical masks in stopping the spread of COVID-19. These findings were mirrored in a January 2023 Cochrane meta-analysis on mask effectiveness. According to the Cochrane report, “The use of a N95/P2 respirators compared to medical/surgical masks probably makes little or no difference for the objective and more precise outcome of laboratory‐confirmed influenza infection.” A May 2023 study published in Ecotoxicology and Environmental Safety suggests N95 respirators may expose wearers to dangerous levels of toxic compounds linked to seizures and cancer. A September 2023 meta-analysis published in Clinical Research Study examined mask studies published since 2019 in the CDC’s Morbidity and Mortality Weekly Report (MMWR). According to the findings of the meta-analysis: “MMWR publications pertaining to masks drew positive conclusions about mask effectiveness >75% of the time despite only 30% testing masks and <15% having statistically significant results. No studies were randomized, yet over half drew causal conclusions. “The level of evidence generated was low and the conclusions were most often unsupported by the data. Our findings raise concern about the reliability of the journal for informing health policy.” Real-world examples also call into question narratives regarding mask efficacy. Sweden, for instance, did not mandate or recommend masks for the general public during the first wave of the COVID-19 pandemic, and only did so in certain situations in the later stages of the pandemic, according to The Conversation. Yet, its total excess deaths during the first two years of the pandemic were among the lowest in Europe.” In 2020, Swedish state epidemiologist Anders Tegnell said, “We see no point in wearing a face mask in Sweden, not even on public transport,” adding there were “at least three heavyweight reports … which all state that the scientific evidence is weak.” A Swedish government commission noted low levels of excess mortality in 2020 and 2021 and said that, at most, masks should have been “recommended.” Soon after the report was released, a Feb. 25, 2022, Boston Herald op-ed stated that Sweden “got it right.” “I don’t understand what is driving the ‘masks work’ political movement,” Thacker told The Defender. “There were plenty of stories written pointing out that there isn’t much scientific evidence that masks stop respiratory virus spread.” “Maybe people were just scared and wanted to believe masks provide protection?” he said. Thacker also cited the historical precedent of the Spanish Flu epidemic in 1918, when the Red Cross campaigned for masks all across America. “California’s state board of health ran a study comparing towns that had mask mandates against those that did not. They found that there was no difference and published the study in the American Journal of Public Health in 1920,” Thacker said. “Maybe these mask campaigners need to read a little history,” he added. Thacker is now calling on whistleblowers inside the CDC to contact him “to discuss what is going on inside the agency.” “I’m talking to CDC people and hope to learn what is going on inside the agency. I plan to write more on this,” Thacker told The Defender. “CDC Director Mandy Cohen wants to restore trust in the agency, but that won’t happen if she keeps putting politics ahead of scientific evidence,” he said. If this content is important to you, share it with your network! Share This article was written by Michael Nevradakis, Ph.D. and originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense. If you find value in this Substack and have the means, please consider making a contribution to support the World Council for Health. Thank you. Upgrade to Paid Subscription Refer a friend Donate Subscriptions Give Direct to WCH https://worldcouncilforhealth.substack.com/p/cdcs-own-scientists-found-masks-ineffective https://donshafi911.blogspot.com/2024/02/cdcs-own-scientists-found-masks_16.html
    WORLDCOUNCILFORHEALTH.SUBSTACK.COM
    CDC’s Own Scientists Found Masks Ineffective for Covid-19 but Recommended Them Anyway
    Officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness
    0 Comments 0 Shares 19417 Views
  • Are You an Anti-Paxxer?

    As doctors drop Paxlovid because of drug interactions and research shows it causes Covid rebounds and virus shedding, Pfizer and MSM crank the PR machine to hide the facts and shame "anti-paxxers."

    Don't fall for it!


    Are You an Anti-Paxxer?
    As doctors drop Paxlovid because of drug interactions and research shows it causes Covid rebounds and virus shedding, Pfizer and MSM crank the PR machine to hide the facts and shame "anti-paxxers."

    Linda Bonvie

    Pfizer has a big public relations push on for its controversial drug Paxlovid. There’s even a name being bandied about for those who question the drug: “Anti-Paxxers.”
    When an article by Los Angeles Times metro reporter Rong-Gong Lin II recommended last month that practically everyone who tests positive for Covid takes Pfizer’s Paxlovid, some media veterans may have wondered what had become of the traditional wall between news reporting and advertising.

    The story, which appeared on January 28, swept away almost all of the reservations that have been raised about the safety and effectiveness of this patent medicine, assuring us that “Paxlovid rebound” is a non-issue and fear of serious side effects is “erroneous.” It even went so far as to suggest that if your doctor won’t prescribe this “highly effective” medication, it’s time to go doctor shopping.

    So why is this LA Times writer so desperately trying to sell us this fast-tracked antiviral that comes with a black box warning?

    The article appeared at a particularly critical time for Pfizer just as it transitions from Emergency Use Authorization, or EUA Paxlovid, to FDA-approved Paxlovid. Originally free to patients, the medication was stockpiled by the U.S. government to the tune of 24 million treatment courses at a cost to taxpayers of $530 a box. Now, the FDA-approved version (same drug, different box) sells for a list price of up to $1,500. (According to an analysis by researchers at Harvard University, the actual cost to Pfizer for a five-day Paxlovid course is $13).

    But to Pfizer’s chagrin, it now doesn’t seem to be able to even give the stuff away, let alone sell it at a premium price. Last fall Pfizer accepted a return of nearly 8 million boxes sent back by the U.S. government.

    What’s a drugmaker to do when both patients and doctors shun a product that was anticipated to be the better half of Pfizer’s post-Covid “multibillion-dollar franchise?

    Flush with all that Covid cash and new Paxlovid FDA approval last May, Pfizer went shopping for partners to help promote its products.

    No stranger to top-tier PR firms such as Edelman and Ogilvy, the drugmaker tagged two of the biggest names in contemporary communications companies, Publicis Groupe, a Paris-based giant PR and ad agency, and the humongous Interpublic Group. These high-level agencies come at a big price tag, but what they can offer is priceless—a way to get your story told by respected media outlets.

    That’s right, if you have enough money to hire the folks with all the right contacts, you too can create your own “news!” And these special contacts are something that PR firms, such as Edelman, are very proud of. Many agency hires, in fact, are recruited directly from major media outlets, such as Edelman NYC Brand Director Nancy Jeffrey, who spent a decade at the Wall Street Journal.

    As quoted in an Edelman website blog, Jeffrey recalls how Richard Edelman (son of founder Dan) would call her during her time working at the paper “to meet a client with a story to tell.” As Jeffrey says, “No one at Edelman ever rises too high to pitch a reporter.”

    So was our LA Times reporter “pitched,” or does he just have an evangelical connection with Paxlovid?

    Let’s take a close look at his story and see what we find.

    Side effects be gone!

    First, there’s the article’s headline, which began: “If it’s COVID, Paxlovid”? Getting your oft-advertised product’s rhyming tagline in a headline—now that’s branding! And we don’t have to tell any of the side effects in this venue. The LA Times piece was off to a great start.

    Why aren’t more people being given Paxlovid, the reporter wanted to know. It’s “cheap or even free for many,” he said. And then he delivered his first rave review, calling it “highly effective.”

    By paragraph four, however, our intrepid reporter had uncovered the bad news that “a number of doctors are still declining to prescribe it.” But why? It must be those pesky “outdated arguments” about “Paxlovid rebound.” Anyone who gets Covid “has a similar rare chance of rebound,” he told us. For extra punch, he called on Dr. Peter Chin-Hong, professor of medicine at UCSF, to back up that statement. Rebound is “like, bogus” and “just dumb,” Chin-Hong said.

    What Lin didn’t report is that a study published in the Annals of Internal Medicine in November 2023, by researchers from Mass General Brigham, found that in Covid patients taking Paxlovid, rebound was “much more common” and often without symptoms. Nearly 21 percent had virologic rebound versus under 2 percent not on the drug. Of perhaps even more significance, prolonged viral shedding for an average of fourteen days was noted in those who rebounded, indicating that they “were potentially still contagious for much longer.” The virologic rebound “phenomenon,” in Paxlovid patients, the authors noted, “has implications for post-N-R (Paxlovid) monitoring and isolation recommendations.” This study closely monitored patients with follow-ups three times a week “sometimes for months.”

    After quoting from several Paxlovid-positive FDA and CDC statements and referencing a California Public Health commercial where people dance to an upbeat tune singing “Test it, treat it, beat it, California you know you need it,” Lin got around to some serious stuff—side effects.

    Not mentioned by Lin, but good to know anyway, Paxlovid bears an FDA-required black-box warning about drug interactions, cautioning of “potentially severe, life-threatening, or fatal events.” But the article carefully danced around this inconvenient issue, simply mentioning that some Paxlovid takers may need to have their medications adjusted. The fear of “serious side effects . . . is largely erroneous,” it claimed.

    Really?

    “There are 125 drug interactions (for Paxlovid) across twenty-five different classes of medicines,” author and FLCCC President Dr. Pierre Kory said in a phone interview. “I’ve never used any medicine that had that number and degree of drug interactions, and I find it absurd,” added Kory, who is an expert in early Covid treatment.

    And this is no secret. The Paxlovid package insert lists thirty-nine specific drugs that interact with this anti-viral (which is not a complete list, we’re warned) including medications that treat conditions such as an enlarged prostate, gout, migraines, high blood pressure, high cholesterol, arrhythmias, and angina.

    With side effects out of the way, our reporter moved on to an interesting idea—doctor shopping.

    If your doctor turns you down for Paxlovid, “what other options are there?” How about “reaching out to another healthcare provider” we’re advised, one “who might be more knowledgeable about Paxlovid . . .”

    Don’t be an ‘Anti-Paxxer!’

    The LA Times isn’t alone in this timely pushing of Paxlovid. The New York Times also ran a glowing Paxlovid piece at the beginning of January. The black-box warning was glossed over by simply saying that some “doctors balk” over the “long list of medications not to be mixed with Paxlovid,” referring to the drug as being “stunningly effective.” The NYT reporter also added five mentions of a study—actually a preprint (not yet peer reviewed or published)—which through the use of statistical magic concluded that during the course of the research had only half of the eligible Covid patients in the U.S. taken Paxlovid, 48,000 lives would have been saved.

    The server where the research was posted warns journalists and others when discussing preprints to “emphasize it has yet to be evaluated by the medical community and information presented may be erroneous.”

    Paxlovid is not the only drug that gets special treatment by the media. Last January, a 60 Minutes segment was called out by the Physicians Committee for Responsible Medicine as “an unlawful weight loss drug ad” for the med Wegovy. The piece, it noted, “looked like a news story, but it was effectively a drug ad,” the group said in a press release. PCRM also stated that Novo Nordisk, which makes Wegovy, paid over $100,000 to the doctors CBS interviewed for the segment.

    With this new frenzy to sell Paxlovid, one can’t help but compare it to the campaign against ivermectin. Kicked off by the FDA in August 2021, it successfully branded this Nobel Prize-winning, FDA-approved drug as nothing more than a horse dewormer endorsed by fanatical outlier doctors and accepted by gullible patients. Despite being found to be an extremely safe treatment as well as an effective one for Covid, the FDA, CDC, and its media “partners” made ivermectin the subject of false accusations and warnings about the supposed risks of using it.

    But early on in the game it was decided, as Dr. Kory pointed out, “to keep the market open for their novel pricey Paxlovid pill.” And to that effect, nothing was going to stand in the way. In an interview last summer with the head of the UCSF Department of Medicine, FDA Commissioner Dr. Robert Califf admitted that he helped promote Paxlovid—something he acknowledged is explicitly against the rules.

    “In normal times, the FDA should not be a cheerleader . . .” Califf said. But since back then EUA drugs could not be advertised (a policy that changed in the fall of 2022) he went ahead and pitched it himself.

    The Paxlovid campaign is far from over. In fact, it may now be revving up to full throttle. There’s even a name being bandied about for those who question the drug: “Anti-Paxxers.”

    And if we can take any insight from the new Pfizer tagline (just filed for protection with the US Patent and Trademark Office), “Outdo Yesterday,” there are even more spurious strategies in its pharmaceutical pipeline.

    Full story:
    https://rescue.substack.com/p/are-you-an-anti-paxxer

    Join @ShankaraChetty


    https://donshafi911.blogspot.com/2024/02/are-you-anti-paxxer-as-doctors-drop.html
    Are You an Anti-Paxxer? 🇺🇸💊As doctors drop Paxlovid because of drug interactions and research shows it causes Covid rebounds and virus shedding, Pfizer and MSM crank the PR machine to hide the facts and shame "anti-paxxers." Don't fall for it! Are You an Anti-Paxxer? As doctors drop Paxlovid because of drug interactions and research shows it causes Covid rebounds and virus shedding, Pfizer and MSM crank the PR machine to hide the facts and shame "anti-paxxers." Linda Bonvie Pfizer has a big public relations push on for its controversial drug Paxlovid. There’s even a name being bandied about for those who question the drug: “Anti-Paxxers.” When an article by Los Angeles Times metro reporter Rong-Gong Lin II recommended last month that practically everyone who tests positive for Covid takes Pfizer’s Paxlovid, some media veterans may have wondered what had become of the traditional wall between news reporting and advertising. The story, which appeared on January 28, swept away almost all of the reservations that have been raised about the safety and effectiveness of this patent medicine, assuring us that “Paxlovid rebound” is a non-issue and fear of serious side effects is “erroneous.” It even went so far as to suggest that if your doctor won’t prescribe this “highly effective” medication, it’s time to go doctor shopping. So why is this LA Times writer so desperately trying to sell us this fast-tracked antiviral that comes with a black box warning? The article appeared at a particularly critical time for Pfizer just as it transitions from Emergency Use Authorization, or EUA Paxlovid, to FDA-approved Paxlovid. Originally free to patients, the medication was stockpiled by the U.S. government to the tune of 24 million treatment courses at a cost to taxpayers of $530 a box. Now, the FDA-approved version (same drug, different box) sells for a list price of up to $1,500. (According to an analysis by researchers at Harvard University, the actual cost to Pfizer for a five-day Paxlovid course is $13). But to Pfizer’s chagrin, it now doesn’t seem to be able to even give the stuff away, let alone sell it at a premium price. Last fall Pfizer accepted a return of nearly 8 million boxes sent back by the U.S. government. What’s a drugmaker to do when both patients and doctors shun a product that was anticipated to be the better half of Pfizer’s post-Covid “multibillion-dollar franchise? Flush with all that Covid cash and new Paxlovid FDA approval last May, Pfizer went shopping for partners to help promote its products. No stranger to top-tier PR firms such as Edelman and Ogilvy, the drugmaker tagged two of the biggest names in contemporary communications companies, Publicis Groupe, a Paris-based giant PR and ad agency, and the humongous Interpublic Group. These high-level agencies come at a big price tag, but what they can offer is priceless—a way to get your story told by respected media outlets. That’s right, if you have enough money to hire the folks with all the right contacts, you too can create your own “news!” And these special contacts are something that PR firms, such as Edelman, are very proud of. Many agency hires, in fact, are recruited directly from major media outlets, such as Edelman NYC Brand Director Nancy Jeffrey, who spent a decade at the Wall Street Journal. As quoted in an Edelman website blog, Jeffrey recalls how Richard Edelman (son of founder Dan) would call her during her time working at the paper “to meet a client with a story to tell.” As Jeffrey says, “No one at Edelman ever rises too high to pitch a reporter.” So was our LA Times reporter “pitched,” or does he just have an evangelical connection with Paxlovid? Let’s take a close look at his story and see what we find. Side effects be gone! First, there’s the article’s headline, which began: “If it’s COVID, Paxlovid”? Getting your oft-advertised product’s rhyming tagline in a headline—now that’s branding! And we don’t have to tell any of the side effects in this venue. The LA Times piece was off to a great start. Why aren’t more people being given Paxlovid, the reporter wanted to know. It’s “cheap or even free for many,” he said. And then he delivered his first rave review, calling it “highly effective.” By paragraph four, however, our intrepid reporter had uncovered the bad news that “a number of doctors are still declining to prescribe it.” But why? It must be those pesky “outdated arguments” about “Paxlovid rebound.” Anyone who gets Covid “has a similar rare chance of rebound,” he told us. For extra punch, he called on Dr. Peter Chin-Hong, professor of medicine at UCSF, to back up that statement. Rebound is “like, bogus” and “just dumb,” Chin-Hong said. What Lin didn’t report is that a study published in the Annals of Internal Medicine in November 2023, by researchers from Mass General Brigham, found that in Covid patients taking Paxlovid, rebound was “much more common” and often without symptoms. Nearly 21 percent had virologic rebound versus under 2 percent not on the drug. Of perhaps even more significance, prolonged viral shedding for an average of fourteen days was noted in those who rebounded, indicating that they “were potentially still contagious for much longer.” The virologic rebound “phenomenon,” in Paxlovid patients, the authors noted, “has implications for post-N-R (Paxlovid) monitoring and isolation recommendations.” This study closely monitored patients with follow-ups three times a week “sometimes for months.” After quoting from several Paxlovid-positive FDA and CDC statements and referencing a California Public Health commercial where people dance to an upbeat tune singing “Test it, treat it, beat it, California you know you need it,” Lin got around to some serious stuff—side effects. Not mentioned by Lin, but good to know anyway, Paxlovid bears an FDA-required black-box warning about drug interactions, cautioning of “potentially severe, life-threatening, or fatal events.” But the article carefully danced around this inconvenient issue, simply mentioning that some Paxlovid takers may need to have their medications adjusted. The fear of “serious side effects . . . is largely erroneous,” it claimed. Really? “There are 125 drug interactions (for Paxlovid) across twenty-five different classes of medicines,” author and FLCCC President Dr. Pierre Kory said in a phone interview. “I’ve never used any medicine that had that number and degree of drug interactions, and I find it absurd,” added Kory, who is an expert in early Covid treatment. And this is no secret. The Paxlovid package insert lists thirty-nine specific drugs that interact with this anti-viral (which is not a complete list, we’re warned) including medications that treat conditions such as an enlarged prostate, gout, migraines, high blood pressure, high cholesterol, arrhythmias, and angina. With side effects out of the way, our reporter moved on to an interesting idea—doctor shopping. If your doctor turns you down for Paxlovid, “what other options are there?” How about “reaching out to another healthcare provider” we’re advised, one “who might be more knowledgeable about Paxlovid . . .” Don’t be an ‘Anti-Paxxer!’ The LA Times isn’t alone in this timely pushing of Paxlovid. The New York Times also ran a glowing Paxlovid piece at the beginning of January. The black-box warning was glossed over by simply saying that some “doctors balk” over the “long list of medications not to be mixed with Paxlovid,” referring to the drug as being “stunningly effective.” The NYT reporter also added five mentions of a study—actually a preprint (not yet peer reviewed or published)—which through the use of statistical magic concluded that during the course of the research had only half of the eligible Covid patients in the U.S. taken Paxlovid, 48,000 lives would have been saved. The server where the research was posted warns journalists and others when discussing preprints to “emphasize it has yet to be evaluated by the medical community and information presented may be erroneous.” Paxlovid is not the only drug that gets special treatment by the media. Last January, a 60 Minutes segment was called out by the Physicians Committee for Responsible Medicine as “an unlawful weight loss drug ad” for the med Wegovy. The piece, it noted, “looked like a news story, but it was effectively a drug ad,” the group said in a press release. PCRM also stated that Novo Nordisk, which makes Wegovy, paid over $100,000 to the doctors CBS interviewed for the segment. With this new frenzy to sell Paxlovid, one can’t help but compare it to the campaign against ivermectin. Kicked off by the FDA in August 2021, it successfully branded this Nobel Prize-winning, FDA-approved drug as nothing more than a horse dewormer endorsed by fanatical outlier doctors and accepted by gullible patients. Despite being found to be an extremely safe treatment as well as an effective one for Covid, the FDA, CDC, and its media “partners” made ivermectin the subject of false accusations and warnings about the supposed risks of using it. But early on in the game it was decided, as Dr. Kory pointed out, “to keep the market open for their novel pricey Paxlovid pill.” And to that effect, nothing was going to stand in the way. In an interview last summer with the head of the UCSF Department of Medicine, FDA Commissioner Dr. Robert Califf admitted that he helped promote Paxlovid—something he acknowledged is explicitly against the rules. “In normal times, the FDA should not be a cheerleader . . .” Califf said. But since back then EUA drugs could not be advertised (a policy that changed in the fall of 2022) he went ahead and pitched it himself. The Paxlovid campaign is far from over. In fact, it may now be revving up to full throttle. There’s even a name being bandied about for those who question the drug: “Anti-Paxxers.” And if we can take any insight from the new Pfizer tagline (just filed for protection with the US Patent and Trademark Office), “Outdo Yesterday,” there are even more spurious strategies in its pharmaceutical pipeline. Full story:👇 https://rescue.substack.com/p/are-you-an-anti-paxxer Join ➡️ @ShankaraChetty https://donshafi911.blogspot.com/2024/02/are-you-anti-paxxer-as-doctors-drop.html
    RESCUE.SUBSTACK.COM
    Are You an Anti-Paxxer?
    As doctors drop Paxlovid because of drug interactions and research shows it causes Covid rebounds and virus shedding, Pfizer and MSM crank the PR machine to hide the facts and shame "anti-paxxers."
    Like
    1
    0 Comments 1 Shares 16995 Views
More Results