• New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging

    SingularityNet, Fetch.ai, and Ocean Protocol are considering merging into AltSignals tokens, targeting a $7.5 billion valuation.
    The merger, led by SingularityNET’s Ben Goertzel and Fetch.ai’s Humayun Sheikh, aims to create a decentralized AI alternative.
    Operational independence will be maintained post-merger, reflecting a trend toward democratizing AI access.
    Artificial intelligence (AI) is set to witness a landmark development as three major protocols, SingularityNet, Fetch.ai, and Ocean Protocol, engage in discussions to merge their tokens into a unified AltSignals token (ASI), potentially boasting a fully diluted valuation of $7.5 billion.
    New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging
    New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging 2
    Read more: SingularityNET Review: Detailed About The Project, Will It Explode With AI Trend?

    SingularityNet, Fetch.ai, and Ocean Protocol Eye Merger With AltSignals Token
    Bloomberg reported on March 27 that the merger aims to establish a decentralized alternative in the AI domain, countering the dominance of tech giants. Pending community approval, the deal could be officially announced as early as Wednesday.

    The collaborative effort seeks to form the largest open-sourced, independent player in AI research and development, affirming a commitment to capitalizing on the AI surge and fostering decentralized infrastructure at scale. SingularityNET CEO Ben Goertzel is scheduled to lead the newly formed Superintelligence Collective, with Fetch.ai CEO Humayun Sheikh serving as chairman.


    AI Trends Are Attracting Attention
    Despite the merger and the establishment of the AltSignals token, SingularityNET, Fetch.ai, and Ocean Protocol will maintain operational autonomy, operating as distinct entities within the collective. This strategic move underscores a broader industry trend toward democratizing AI access, challenging the dominance of corporate giants like Alphabet and Microsoft.

    The convergence of these leading AI platforms mirrors a broader trend within the crypto market, where entities are increasingly exploring opportunities in AI development. Notably, Tether, a prominent stablecoin issuer, has recently announced plans to venture into open-source AI models, highlighting a growing synergy between AI and blockchain technologies in addressing real-world challenges.
    New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging SingularityNet, Fetch.ai, and Ocean Protocol are considering merging into AltSignals tokens, targeting a $7.5 billion valuation. The merger, led by SingularityNET’s Ben Goertzel and Fetch.ai’s Humayun Sheikh, aims to create a decentralized AI alternative. Operational independence will be maintained post-merger, reflecting a trend toward democratizing AI access. Artificial intelligence (AI) is set to witness a landmark development as three major protocols, SingularityNet, Fetch.ai, and Ocean Protocol, engage in discussions to merge their tokens into a unified AltSignals token (ASI), potentially boasting a fully diluted valuation of $7.5 billion. New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging 2 Read more: SingularityNET Review: Detailed About The Project, Will It Explode With AI Trend? SingularityNet, Fetch.ai, and Ocean Protocol Eye Merger With AltSignals Token Bloomberg reported on March 27 that the merger aims to establish a decentralized alternative in the AI domain, countering the dominance of tech giants. Pending community approval, the deal could be officially announced as early as Wednesday. The collaborative effort seeks to form the largest open-sourced, independent player in AI research and development, affirming a commitment to capitalizing on the AI surge and fostering decentralized infrastructure at scale. SingularityNET CEO Ben Goertzel is scheduled to lead the newly formed Superintelligence Collective, with Fetch.ai CEO Humayun Sheikh serving as chairman. AI Trends Are Attracting Attention Despite the merger and the establishment of the AltSignals token, SingularityNET, Fetch.ai, and Ocean Protocol will maintain operational autonomy, operating as distinct entities within the collective. This strategic move underscores a broader industry trend toward democratizing AI access, challenging the dominance of corporate giants like Alphabet and Microsoft. The convergence of these leading AI platforms mirrors a broader trend within the crypto market, where entities are increasingly exploring opportunities in AI development. Notably, Tether, a prominent stablecoin issuer, has recently announced plans to venture into open-source AI models, highlighting a growing synergy between AI and blockchain technologies in addressing real-world challenges.
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  • New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging

    SingularityNet, Fetch.ai, and Ocean Protocol are considering merging into AltSignals tokens, targeting a $7.5 billion valuation.
    The merger, led by SingularityNET’s Ben Goertzel and Fetch.ai’s Humayun Sheikh, aims to create a decentralized AI alternative.
    Operational independence will be maintained post-merger, reflecting a trend toward democratizing AI access.
    Artificial intelligence (AI) is set to witness a landmark development as three major protocols, SingularityNet, Fetch.ai, and Ocean Protocol, engage in discussions to merge their tokens into a unified AltSignals token (ASI), potentially boasting a fully diluted valuation of $7.5 billion.
    New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging
    New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging 2
    Read more: SingularityNET Review: Detailed About The Project, Will It Explode With AI Trend?

    SingularityNet, Fetch.ai, and Ocean Protocol Eye Merger With AltSignals Token
    Bloomberg reported on March 27 that the merger aims to establish a decentralized alternative in the AI domain, countering the dominance of tech giants. Pending community approval, the deal could be officially announced as early as Wednesday.

    The collaborative effort seeks to form the largest open-sourced, independent player in AI research and development, affirming a commitment to capitalizing on the AI surge and fostering decentralized infrastructure at scale. SingularityNET CEO Ben Goertzel is scheduled to lead the newly formed Superintelligence Collective, with Fetch.ai CEO Humayun Sheikh serving as chairman.


    AI Trends Are Attracting Attention
    Despite the merger and the establishment of the AltSignals token, SingularityNET, Fetch.ai, and Ocean Protocol will maintain operational autonomy, operating as distinct entities within the collective. This strategic move underscores a broader industry trend toward democratizing AI access, challenging the dominance of corporate giants like Alphabet and Microsoft.

    The convergence of these leading AI platforms mirrors a broader trend within the crypto market, where entities are increasingly exploring opportunities in AI development. Notably, Tether, a prominent stablecoin issuer, has recently announced plans to venture into open-source AI models, highlighting a growing synergy between AI and blockchain technologies in addressing real-world challenges.
    New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging SingularityNet, Fetch.ai, and Ocean Protocol are considering merging into AltSignals tokens, targeting a $7.5 billion valuation. The merger, led by SingularityNET’s Ben Goertzel and Fetch.ai’s Humayun Sheikh, aims to create a decentralized AI alternative. Operational independence will be maintained post-merger, reflecting a trend toward democratizing AI access. Artificial intelligence (AI) is set to witness a landmark development as three major protocols, SingularityNet, Fetch.ai, and Ocean Protocol, engage in discussions to merge their tokens into a unified AltSignals token (ASI), potentially boasting a fully diluted valuation of $7.5 billion. New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging 2 Read more: SingularityNET Review: Detailed About The Project, Will It Explode With AI Trend? SingularityNet, Fetch.ai, and Ocean Protocol Eye Merger With AltSignals Token Bloomberg reported on March 27 that the merger aims to establish a decentralized alternative in the AI domain, countering the dominance of tech giants. Pending community approval, the deal could be officially announced as early as Wednesday. The collaborative effort seeks to form the largest open-sourced, independent player in AI research and development, affirming a commitment to capitalizing on the AI surge and fostering decentralized infrastructure at scale. SingularityNET CEO Ben Goertzel is scheduled to lead the newly formed Superintelligence Collective, with Fetch.ai CEO Humayun Sheikh serving as chairman. AI Trends Are Attracting Attention Despite the merger and the establishment of the AltSignals token, SingularityNET, Fetch.ai, and Ocean Protocol will maintain operational autonomy, operating as distinct entities within the collective. This strategic move underscores a broader industry trend toward democratizing AI access, challenging the dominance of corporate giants like Alphabet and Microsoft. The convergence of these leading AI platforms mirrors a broader trend within the crypto market, where entities are increasingly exploring opportunities in AI development. Notably, Tether, a prominent stablecoin issuer, has recently announced plans to venture into open-source AI models, highlighting a growing synergy between AI and blockchain technologies in addressing real-world challenges.
    0 Σχόλια 0 Μοιράστηκε 32 Views
  • Win Real Money Online Instantly: Proven Methods for Immediate Financial Gain

    Win Real Money Online Instantly Join Here 👇👇
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    In recent years, the quest to win real money online instantly has driven many towards innovative online platforms. Games like Slots Cash™ on the App Store and mobile gaming platforms provided by Skillz showcase how digital arenas are becoming lucrative sources of income for players worldwide 12. With platforms such as Swagbucks and InboxDollars, individuals have multiple pathways to earn by engaging in games, surveys, and various online tasks, enhancing the accessibility to instant financial gains 2.

    As technology advances, options to win span across a broad spectrum, including traditional and digital game forms. From classic slots with high Return to Player (RTP) percentages like Mega Joker and Blood Suckers, to engaging in the gig economy through apps that offer micro-jobs, users have a plethora of opportunities to win real money online instantly 32. This article explores proven methods for immediate financial gain, delving into the worlds of cashback apps, cryptocurrency, stock trading platforms, and more, providing readers with insights on navigating the digital landscape profitably.

    Exploring Micro-Jobs and Gig Economy Platforms

    Exploring the gig economy and micro-job platforms unveils a dynamic landscape where individuals can monetize their skills and services efficiently. Key platforms facilitating this include:

    Appen and Clickworker: Specializing in tasks that train artificial intelligence, ranging from object recognition in images to human interaction simulations 7.
    Amazon Mechanical Turk and Neevo: Offering a wide array of micro-tasks, these platforms help businesses outsource small, yet significant tasks, such as data annotation and manual task training for AI 7.
    Fiverr and Upwork: These platforms allow professionals to sell their services across various fields like design, writing, and music, catering to a broad audience looking for specialized skills 8.
    Moreover, platforms like TaskRabbit and PeoplePerHour provide opportunities for individuals to offer their services both locally and globally, thus expanding the potential for financial gain 89. The gig economy's flexibility and the diversity of available tasks make it an attractive option for those looking to win real money online instantly 6789.

    Leveraging Cashback and Rebate Apps

    Leveraging cashback and rebate apps is a savvy strategy for those looking to win real money online instantly. These apps offer a variety of ways to earn back a portion of your spending through everyday purchases, dining, and even travel. Here's a breakdown of some top-rated apps and their unique features:

    Ibotta and Rakuten: Both apps provide users with cashback on a wide range of shopping options. Ibotta requires users to activate offers and clip digital coupons, while Rakuten offers cash back on eligible purchases through their platform or browser extension. Users can receive their savings via bank deposit, PayPal, or gift cards once they reach the minimum threshold 12.
    Dosh and Upside: Dosh offers automatic cashback without the need to scan receipts, making it a hassle-free option. Upside provides cashback at grocery stores, restaurants, and gas stations, with some users earning up to 25 cents back per gallon of gas 1213.
    Specialty Apps:Fetch: Redeem any purchase receipts for points, exchangeable for gift cards. Despite some users finding it slow to accumulate rewards, the app boasts high ratings 11.Coupons.com: Online Promo Codes and Free Printable Coupons: Focuses on grocery coupons, automatically applying discounts when you link your store loyalty card 11.RetailMeNot: Known for coupons, this app also offers a cashback program, though not all stores participate 11.
    Each app has its own set of advantages and potential drawbacks, from ease of use to the range of participating retailers. By choosing the right combination of apps, users can maximize their cashback earnings and move closer to achieving their goal of winning real money online instantly 10111213.

    Win Real Money Online Instantly Here is the Way 👇👇
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    Participating in the Sharing Economy

    Participating in the sharing economy can be a lucrative way to win real money online instantly. This sector allows individuals to capitalize on their unused or spare resources, from accommodation and transportation to personal belongings and skills. Here are some key opportunities:

    Accommodation & Space:List empty rooms or entire houses on platforms like Airbnb, Vrbo, or Booking.com: The largest selection of hotels, homes, and vacation rentals 14.Rent out underutilized spaces such as driveways, gardens, or parking spots through Neighbor | The Cheaper, Closer & Safer Storage Marketplace or Campspace 16.
    Transportation:Share your car via Turo or Getaround, or become a ride-sharing driver with Uber or Lyft 14.Unique options like turning your car into a moving billboard with Carvertise - Advertise On Uber, Lyft, and Grubhub Cars offer additional income streams 14.
    Personal Belongings & Skills:Platforms like Poshmark or Spinlister allow you to rent out clothes or sports equipment 14.Share your knowledge by creating online courses on Udemy or Teachable 14.
    The sharing economy's flexibility and low entry barriers make it an appealing option for those looking to supplement their income. With the industry projected to grow significantly, exploring these avenues could lead to substantial financial benefits 17.

    Investing in Cryptocurrency and Stock Trading Apps

    Investing in the digital currency and stock markets offers a diverse range of options for those aiming to win real money online instantly. Key platforms and their features include:

    Cryptocurrency Exchanges:Crypto Trading Platform | Buy, Sell, & Trade Crypto in the US | Binance.US: Offers trading in over 150 coins with fees starting at 0.57 percent for less-common coins, decreasing for high-volume traders. A 5 percent discount on fees is available with BNB payment 19.Coinbase: Known for its wide selection of cryptocurrencies, with fees typically at least 1.99 percent. Lower fees are available through Coinbase Advanced Trade 19.Kraken: Features a vast selection of 236 cryptocurrencies, with fees starting at 0.26 percent. Additional fees apply for card and online banking transactions 19.
    Stock and Cryptocurrency Trading Apps:Robinhood: Offers commission-free trading in stocks, ETFs, options, and cryptocurrencies, making it a popular choice for beginners. No minimum deposit required 22.E*TRADE: Provides a user-friendly mobile app and access to a wide range of investment options including stocks, options, ETFs, and mutual funds. Charges $0 commission for online US-listed stock, ETF, and options trades 22.TD Ameritrade: Known for its educational resources and tools, this platform also offers a robust mobile app and access to a broad spectrum of investment options. No minimum deposit required 22.
    These platforms provide various features tailored to different investing needs, from simple peer-to-peer payments to advanced trading strategies. By carefully selecting the right platform, individuals can enhance their prospects of financial gain in the digital marketplace 18192022.

    Conclusion

    This exploration into the myriad ways to win real money online has illuminated a diverse landscape of opportunities, each catering to different interests, skills, and investment levels. The gig economy, cashback and rebate apps, the sharing economy, and digital investing platforms are proven pathways that can lead to immediate financial gain. These methods reinforce the notion that with the right strategies and platforms, individuals can effectively navigate the digital realm to enhance their financial situation.

    Moreover, the significance of these opportunities extends beyond individual gain, highlighting a shift towards a more accessible and flexible economic landscape. As we venture further into this digital era, the potential for innovation and growth in these areas is immense, promising even more avenues for financial success. Embracing these options not only offers immediate benefits but also sets the stage for ongoing financial empowerment and independence, urging readers to explore these avenues with keen interest and informed perspective.

    FAQs

    How can I quickly earn legitimate money?

    To earn money quickly and legitimately, you can adopt various strategies such as:

    Driving for rideshare services
    Freelancing in your area of expertise
    Selling unused gift cards
    Renting out your car or parking space
    Referring friends to apps
    Searching for unclaimed money
    Delivering groceries or takeout
    Selling your clothes online
    What apps can pay me real money immediately?

    Some popular apps that pay out real money instantly include:

    Gaming Apps: Play games and compete with others for rewards (e.g., Mistplay, Lucktastic, Swagbucks Games).
    Survey Apps: Provide your opinions on various products and services to earn cash or gift cards.
    What are some methods to get money right away?

    You can obtain money instantly by:

    Selling spare electronics
    Selling unused gift cards
    Pawning items
    Working for immediate pay
    Seeking community loans and assistance
    Requesting bill forbearance
    Asking for a payroll advance
    Which app is the most trustworthy for earning money?

    Some of the most reliable apps for making money include:

    Swagbucks: Best for earning gift cards
    Survey Junkie: Best for completing online surveys
    Rocket Money: Best for managing finances
    DoorDash: Best for delivery drivers
    Rakuten Rewards: Best for cash back on purchases
    Upside: Best for rewards at gas stations
    Upwork: Best for freelancers looking for gigs

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    #onlinemoney #makemoney #realmoney #cashapp #giveaway #cashappblessing #giftcard #freegiftcard
    Win Real Money Online Instantly: Proven Methods for Immediate Financial Gain Win Real Money Online Instantly Join Here 👇👇 https://grabify.link/S7MPC7 In recent years, the quest to win real money online instantly has driven many towards innovative online platforms. Games like Slots Cash™ on the App Store and mobile gaming platforms provided by Skillz showcase how digital arenas are becoming lucrative sources of income for players worldwide 12. With platforms such as Swagbucks and InboxDollars, individuals have multiple pathways to earn by engaging in games, surveys, and various online tasks, enhancing the accessibility to instant financial gains 2. As technology advances, options to win span across a broad spectrum, including traditional and digital game forms. From classic slots with high Return to Player (RTP) percentages like Mega Joker and Blood Suckers, to engaging in the gig economy through apps that offer micro-jobs, users have a plethora of opportunities to win real money online instantly 32. This article explores proven methods for immediate financial gain, delving into the worlds of cashback apps, cryptocurrency, stock trading platforms, and more, providing readers with insights on navigating the digital landscape profitably. Exploring Micro-Jobs and Gig Economy Platforms Exploring the gig economy and micro-job platforms unveils a dynamic landscape where individuals can monetize their skills and services efficiently. Key platforms facilitating this include: Appen and Clickworker: Specializing in tasks that train artificial intelligence, ranging from object recognition in images to human interaction simulations 7. Amazon Mechanical Turk and Neevo: Offering a wide array of micro-tasks, these platforms help businesses outsource small, yet significant tasks, such as data annotation and manual task training for AI 7. Fiverr and Upwork: These platforms allow professionals to sell their services across various fields like design, writing, and music, catering to a broad audience looking for specialized skills 8. Moreover, platforms like TaskRabbit and PeoplePerHour provide opportunities for individuals to offer their services both locally and globally, thus expanding the potential for financial gain 89. The gig economy's flexibility and the diversity of available tasks make it an attractive option for those looking to win real money online instantly 6789. Leveraging Cashback and Rebate Apps Leveraging cashback and rebate apps is a savvy strategy for those looking to win real money online instantly. These apps offer a variety of ways to earn back a portion of your spending through everyday purchases, dining, and even travel. Here's a breakdown of some top-rated apps and their unique features: Ibotta and Rakuten: Both apps provide users with cashback on a wide range of shopping options. Ibotta requires users to activate offers and clip digital coupons, while Rakuten offers cash back on eligible purchases through their platform or browser extension. Users can receive their savings via bank deposit, PayPal, or gift cards once they reach the minimum threshold 12. Dosh and Upside: Dosh offers automatic cashback without the need to scan receipts, making it a hassle-free option. Upside provides cashback at grocery stores, restaurants, and gas stations, with some users earning up to 25 cents back per gallon of gas 1213. Specialty Apps:Fetch: Redeem any purchase receipts for points, exchangeable for gift cards. Despite some users finding it slow to accumulate rewards, the app boasts high ratings 11.Coupons.com: Online Promo Codes and Free Printable Coupons: Focuses on grocery coupons, automatically applying discounts when you link your store loyalty card 11.RetailMeNot: Known for coupons, this app also offers a cashback program, though not all stores participate 11. Each app has its own set of advantages and potential drawbacks, from ease of use to the range of participating retailers. By choosing the right combination of apps, users can maximize their cashback earnings and move closer to achieving their goal of winning real money online instantly 10111213. Win Real Money Online Instantly Here is the Way 👇👇 https://grabify.link/S7MPC7 Participating in the Sharing Economy Participating in the sharing economy can be a lucrative way to win real money online instantly. This sector allows individuals to capitalize on their unused or spare resources, from accommodation and transportation to personal belongings and skills. Here are some key opportunities: Accommodation & Space:List empty rooms or entire houses on platforms like Airbnb, Vrbo, or Booking.com: The largest selection of hotels, homes, and vacation rentals 14.Rent out underutilized spaces such as driveways, gardens, or parking spots through Neighbor | The Cheaper, Closer & Safer Storage Marketplace or Campspace 16. Transportation:Share your car via Turo or Getaround, or become a ride-sharing driver with Uber or Lyft 14.Unique options like turning your car into a moving billboard with Carvertise - Advertise On Uber, Lyft, and Grubhub Cars offer additional income streams 14. Personal Belongings & Skills:Platforms like Poshmark or Spinlister allow you to rent out clothes or sports equipment 14.Share your knowledge by creating online courses on Udemy or Teachable 14. The sharing economy's flexibility and low entry barriers make it an appealing option for those looking to supplement their income. With the industry projected to grow significantly, exploring these avenues could lead to substantial financial benefits 17. Investing in Cryptocurrency and Stock Trading Apps Investing in the digital currency and stock markets offers a diverse range of options for those aiming to win real money online instantly. Key platforms and their features include: Cryptocurrency Exchanges:Crypto Trading Platform | Buy, Sell, & Trade Crypto in the US | Binance.US: Offers trading in over 150 coins with fees starting at 0.57 percent for less-common coins, decreasing for high-volume traders. A 5 percent discount on fees is available with BNB payment 19.Coinbase: Known for its wide selection of cryptocurrencies, with fees typically at least 1.99 percent. Lower fees are available through Coinbase Advanced Trade 19.Kraken: Features a vast selection of 236 cryptocurrencies, with fees starting at 0.26 percent. Additional fees apply for card and online banking transactions 19. Stock and Cryptocurrency Trading Apps:Robinhood: Offers commission-free trading in stocks, ETFs, options, and cryptocurrencies, making it a popular choice for beginners. No minimum deposit required 22.E*TRADE: Provides a user-friendly mobile app and access to a wide range of investment options including stocks, options, ETFs, and mutual funds. Charges $0 commission for online US-listed stock, ETF, and options trades 22.TD Ameritrade: Known for its educational resources and tools, this platform also offers a robust mobile app and access to a broad spectrum of investment options. No minimum deposit required 22. These platforms provide various features tailored to different investing needs, from simple peer-to-peer payments to advanced trading strategies. By carefully selecting the right platform, individuals can enhance their prospects of financial gain in the digital marketplace 18192022. Conclusion This exploration into the myriad ways to win real money online has illuminated a diverse landscape of opportunities, each catering to different interests, skills, and investment levels. The gig economy, cashback and rebate apps, the sharing economy, and digital investing platforms are proven pathways that can lead to immediate financial gain. These methods reinforce the notion that with the right strategies and platforms, individuals can effectively navigate the digital realm to enhance their financial situation. Moreover, the significance of these opportunities extends beyond individual gain, highlighting a shift towards a more accessible and flexible economic landscape. As we venture further into this digital era, the potential for innovation and growth in these areas is immense, promising even more avenues for financial success. Embracing these options not only offers immediate benefits but also sets the stage for ongoing financial empowerment and independence, urging readers to explore these avenues with keen interest and informed perspective. FAQs How can I quickly earn legitimate money? To earn money quickly and legitimately, you can adopt various strategies such as: Driving for rideshare services Freelancing in your area of expertise Selling unused gift cards Renting out your car or parking space Referring friends to apps Searching for unclaimed money Delivering groceries or takeout Selling your clothes online What apps can pay me real money immediately? Some popular apps that pay out real money instantly include: Gaming Apps: Play games and compete with others for rewards (e.g., Mistplay, Lucktastic, Swagbucks Games). Survey Apps: Provide your opinions on various products and services to earn cash or gift cards. What are some methods to get money right away? You can obtain money instantly by: Selling spare electronics Selling unused gift cards Pawning items Working for immediate pay Seeking community loans and assistance Requesting bill forbearance Asking for a payroll advance Which app is the most trustworthy for earning money? Some of the most reliable apps for making money include: Swagbucks: Best for earning gift cards Survey Junkie: Best for completing online surveys Rocket Money: Best for managing finances DoorDash: Best for delivery drivers Rakuten Rewards: Best for cash back on purchases Upside: Best for rewards at gas stations Upwork: Best for freelancers looking for gigs Win Real Money Instantly Here 👇👇 https://grabify.link/S7MPC7 #onlinemoney #makemoney #realmoney #cashapp #giveaway #cashappblessing #giftcard #freegiftcard
    0 Σχόλια 0 Μοιράστηκε 2936 Views
  • "It is obviously un-American for the government to develop a ‘hit list’ of citizens to mute in the public square through secret pressure on communications monopolies."

    This Country Can't Afford A SCOTUS Weak On Internet Censorship
    Joy Pullmann
    The Biden administration attempted to distract the Supreme Court from the voluminous evidence of federal abuse of Americans’ speech rights during oral arguments in Murthy v. Missouri Monday. It sounded like several justices followed the feds’ waving red flag.

    “The government may not use coercive threats to suppress speech, but it is entitled to speak for itself by informing, persuading, or criticizing private speakers,” said Biden administration lawyer Brian Fletcher in his opening remarks. He and several justices asserted government speech prerogatives that would flip the Constitution upside down.

    The government doesn’t have constitutional rights. Constitutional rights belong to the people and restrain the government. The people’s right to speak may not be abridged. Government officials’ speaking, in their official capacities, may certainly be abridged. Indeed, it often must be, precisely to restrict officials from abusing the state’s monopoly on violence to bully citizens into serfdom.

    It is obviously un-American and unconstitutional for the government to develop a “hit list” of citizens to mute in the public square through secret pressure on communications monopolies beholden to the government for their monopoly powers. There is simply no way it’s “protected speech” for the feds to use intermediaries to silence anyone who disagrees with them on internet forums where the majority of the nation’s political organizing and information dissemination occurs.

    Bullying, Not the Bully Pulpit

    What’s happening is not government expressing its views to media, or “encouraging press to suppress their own speech,” as Justice Elena Kagan put it. This is government bullying third parties to suppress Americans’ speech that officials dislike.

    In the newspaper analogy, it would be like government threatening an IRS audit or Equal Employment Opportunity Commission (EEOC) investigation, or pulling the business license of The Washington Post if the Post published an op-ed from Jay Bhattacharya. As Norwood v. Harrison established in 1973, that’s blatantly unconstitutional. Government cannot “induce, encourage or promote private persons to accomplish what it is constitutionally forbidden to accomplish.”

    Yet, notes Matt Taibbi, some justices and Fletcher “re-framed the outing of extravagantly funded, ongoing content-flagging programs, designed by veterans of foreign counterterrorism operations and targeting the domestic population, as a debate about what Fletcher called ‘classic bully pulpit exhortations.’”

    Every Fake Excuse for Censorship Is Already Illegal

    We have laws against all the harms the government and several justices put forth as excuses for government censorship. Terrorism is illegal. Promoting terrorism is illegal, as an incitement to treason and violence. Inciting children to injure or murder themselves by jumping out windows — a “hypothetical” brought up by Justice Ketanji Brown Jackson and discussed at length in oral arguments — is illegal.

    If someone is spreading terrorist incitements to violence on Facebook, law enforcement needs to go after the terrorist plotters, not Facebook. Just like it’s unjust to punish gun, knife, and tire iron manufacturers for the people who use their products to murder, it’s unjust and unconstitutional for government to effectively commandeer Facebook under the pretext of all the evils people use it to spread. If they have a problem with those evils, they should address those evils directly, not pressure Facebook to do what they can’t get through Congress like it’s some kind of substitute legislature.

    It’s also ridiculous to, as Jackson and Fletcher did in oral argument, assume that the government is the only possible solution to every social ill. Do these hypothetically window-jumping children not have parents? Teachers? Older siblings? Neighbors? Would the social media companies not have an interest in preventing their products from being used to promote death, and wouldn’t that be an easy thing to explain publicly? Apparently, Jackson couldn’t conceive of any other solution to problems like these than government censorship, when our society has handled far bigger problems like war, pandemics, and foreign invasion without government censorship for 250 years!

    Voters Auditing Government Is Exactly How Our System Should Work

    Fletcher described it as a “problem” that in this case, “two states and five individuals are trying to use the Article III courts to audit all of the executive branch’s communications with and about social media platforms.” That’s called transparency, and it’s only a problem if the government is trying to escape accountability to voters for its actions.

    The people have a fundamental right to audit what their government is doing with public positions, institutions, and funds! How do we have government by consent of the governed if the people can have no idea what their government is doing?

    Under federal laws, all communications like those this lawsuit uncovered are public records. Yet these public records are really hard to get. The executive branch has been effectively nullifying open records laws by absurdly lengthening disclosure times — to as long as 636 days — increasingly forcing citizens to wage expensive lawsuits to get federal agencies to cough up records years beyond the legal deadline.

    Congress should pass a law forcing the automatic disclosure of all government communications with tech monopolies that don’t concern actual classified information and “national security” designations, which the government expands unlawfully to avoid transparency. No justice should support government secrecy about its speech pressure efforts outside of legitimate national security actions.

    Government Is So Big, It’s Always Coercive

    Fletcher’s argument also claimed to draw a line between government persuasion and government coercion. The size and minute harassment powers of our government long ago obliterated any such line, if it ever existed. Federal agencies now have the power to try citizens in non-Article III courts, outside constitutional protections for due process. Citizens can be bankrupted long before they finally get to appeal to a real court. That’s why most of them just do whatever the agencies say, even when it’s clearly unlawful.

    Federal agencies demand power over almost every facet of life, from puddles in people’s backyards to the temperature of cheese served in a tiny restaurant. If they put a target on any normal citizen’s back, he goes bankrupt after regulatory torture.

    As Franklin Roosevelt’s “brain trust” planned, government is now the “senior partner” of every business, giving every “request” from government officials automatic coercion power. Federal agencies have six ways from Sunday of getting back at a noncompliant company, from the EEOC to the Occupational Safety and Health Administration to the Environmental Protection Agency to Health and Human Services to Securities and Exchange Commission investigations and more. Use an accurate pronoun? Investigation. Hire “one too many” white guys? Investigation.

    TikTok legislation going through Congress right now would codify federal power to seize social media companies accused of being owned by foreign interests. Shortly after he acquired X, Elon Musk faced a regulatory shakedown costing him tens of millions, and more on the way. He has money like that, but the rest of us don’t.

    Speech from a private citizen does not have the threat of violence behind it. Speech from a government official, on the other hand, absolutely does and always has. Government officials have powers that other people don’t, and those powers are easily abused, which is exactly why we have a Constitution. SCOTUS needs to take this crucial context into account, making constitutional protections stronger because the government is far, far outside its constitutional bounds.

    Big tech companies’ very business model depends on government regulators and can be destroyed — or kneecapped — at the stroke of an activist president’s pen. Or, at least, that’s what the president said when Facebook and Twitter didn’t do what he wanted: Section 230 should “immediately be revoked.” This is a president who claims the executive power to unilaterally rewrite laws, ignore laws, and ignore Supreme Court decisions. It’s a president who issues orders as press releases so they go into effect months before they can even begin to be challenged in court.

    Constitutionally Protected Speech Isn’t Terrorism

    If justices buy the administration’s nice-guy pretenses of “concern about terrorism,” and “once in a lifetime pandemic measures,” they didn’t read the briefs in this case and see that is simply a cover for the U.S. government turning counterterrorism tools on its own citizens in an attempt to control election outcomes. This is precisely what the First Amendment was designed to check, and we Americans need our Supreme Court to understand that and act to protect us. Elections mean nothing when the government is secretly keeping voters from talking to each other.

    The Supreme Court may not be able to return the country to full constitutional government by eradicating the almost entirely unconstitutional administrative state. But it should enforce as many constitutional boundaries as possible on such agencies. That clearly includes prohibiting all of government from outsourcing to allegedly “private” organizations actions that would be illegal for the government to take.

    That includes not just coercive instructions to social media companies, but also developing social media censorship tools and organizations as cutouts for the rogue security state that is targeting peaceful citizens instead of actual terrorists. Even false speech is not domestic terrorism, and no clearheaded Supreme Court justice looking at the evidence could let the Biden administration weaponize antiterrorism measures to strip law-abiding Americans of our fundamental human rights.

    Joy Pullmann is executive editor of The Federalist, a happy wife, and the mother of six children. Her ebooks include "Classic Books For Young Children," and "101 Strategies For Living Well Amid Inflation." An 18-year education and politics reporter, Joy has testified before nearly two dozen legislatures on education policy and appeared on major media from Fox News to Ben Shapiro to Dennis Prager. Joy is a grateful graduate of the Hillsdale College honors and journalism programs who identifies as native American and gender natural. Her traditionally published books include "The Education Invasion: How Common Core Fights Parents for Control of American Kids," from Encounter Books.


    https://thefederalist.com/2024/03/21/this-country-cannot-afford-a-weak-supreme-court-decision-on-internet-censorship/

    Join ➡️ @MartinKulldorf
    "It is obviously un-American for the government to develop a ‘hit list’ of citizens to mute in the public square through secret pressure on communications monopolies." This Country Can't Afford A SCOTUS Weak On Internet Censorship Joy Pullmann The Biden administration attempted to distract the Supreme Court from the voluminous evidence of federal abuse of Americans’ speech rights during oral arguments in Murthy v. Missouri Monday. It sounded like several justices followed the feds’ waving red flag. “The government may not use coercive threats to suppress speech, but it is entitled to speak for itself by informing, persuading, or criticizing private speakers,” said Biden administration lawyer Brian Fletcher in his opening remarks. He and several justices asserted government speech prerogatives that would flip the Constitution upside down. The government doesn’t have constitutional rights. Constitutional rights belong to the people and restrain the government. The people’s right to speak may not be abridged. Government officials’ speaking, in their official capacities, may certainly be abridged. Indeed, it often must be, precisely to restrict officials from abusing the state’s monopoly on violence to bully citizens into serfdom. It is obviously un-American and unconstitutional for the government to develop a “hit list” of citizens to mute in the public square through secret pressure on communications monopolies beholden to the government for their monopoly powers. There is simply no way it’s “protected speech” for the feds to use intermediaries to silence anyone who disagrees with them on internet forums where the majority of the nation’s political organizing and information dissemination occurs. Bullying, Not the Bully Pulpit What’s happening is not government expressing its views to media, or “encouraging press to suppress their own speech,” as Justice Elena Kagan put it. This is government bullying third parties to suppress Americans’ speech that officials dislike. In the newspaper analogy, it would be like government threatening an IRS audit or Equal Employment Opportunity Commission (EEOC) investigation, or pulling the business license of The Washington Post if the Post published an op-ed from Jay Bhattacharya. As Norwood v. Harrison established in 1973, that’s blatantly unconstitutional. Government cannot “induce, encourage or promote private persons to accomplish what it is constitutionally forbidden to accomplish.” Yet, notes Matt Taibbi, some justices and Fletcher “re-framed the outing of extravagantly funded, ongoing content-flagging programs, designed by veterans of foreign counterterrorism operations and targeting the domestic population, as a debate about what Fletcher called ‘classic bully pulpit exhortations.’” Every Fake Excuse for Censorship Is Already Illegal We have laws against all the harms the government and several justices put forth as excuses for government censorship. Terrorism is illegal. Promoting terrorism is illegal, as an incitement to treason and violence. Inciting children to injure or murder themselves by jumping out windows — a “hypothetical” brought up by Justice Ketanji Brown Jackson and discussed at length in oral arguments — is illegal. If someone is spreading terrorist incitements to violence on Facebook, law enforcement needs to go after the terrorist plotters, not Facebook. Just like it’s unjust to punish gun, knife, and tire iron manufacturers for the people who use their products to murder, it’s unjust and unconstitutional for government to effectively commandeer Facebook under the pretext of all the evils people use it to spread. If they have a problem with those evils, they should address those evils directly, not pressure Facebook to do what they can’t get through Congress like it’s some kind of substitute legislature. It’s also ridiculous to, as Jackson and Fletcher did in oral argument, assume that the government is the only possible solution to every social ill. Do these hypothetically window-jumping children not have parents? Teachers? Older siblings? Neighbors? Would the social media companies not have an interest in preventing their products from being used to promote death, and wouldn’t that be an easy thing to explain publicly? Apparently, Jackson couldn’t conceive of any other solution to problems like these than government censorship, when our society has handled far bigger problems like war, pandemics, and foreign invasion without government censorship for 250 years! Voters Auditing Government Is Exactly How Our System Should Work Fletcher described it as a “problem” that in this case, “two states and five individuals are trying to use the Article III courts to audit all of the executive branch’s communications with and about social media platforms.” That’s called transparency, and it’s only a problem if the government is trying to escape accountability to voters for its actions. The people have a fundamental right to audit what their government is doing with public positions, institutions, and funds! How do we have government by consent of the governed if the people can have no idea what their government is doing? Under federal laws, all communications like those this lawsuit uncovered are public records. Yet these public records are really hard to get. The executive branch has been effectively nullifying open records laws by absurdly lengthening disclosure times — to as long as 636 days — increasingly forcing citizens to wage expensive lawsuits to get federal agencies to cough up records years beyond the legal deadline. Congress should pass a law forcing the automatic disclosure of all government communications with tech monopolies that don’t concern actual classified information and “national security” designations, which the government expands unlawfully to avoid transparency. No justice should support government secrecy about its speech pressure efforts outside of legitimate national security actions. Government Is So Big, It’s Always Coercive Fletcher’s argument also claimed to draw a line between government persuasion and government coercion. The size and minute harassment powers of our government long ago obliterated any such line, if it ever existed. Federal agencies now have the power to try citizens in non-Article III courts, outside constitutional protections for due process. Citizens can be bankrupted long before they finally get to appeal to a real court. That’s why most of them just do whatever the agencies say, even when it’s clearly unlawful. Federal agencies demand power over almost every facet of life, from puddles in people’s backyards to the temperature of cheese served in a tiny restaurant. If they put a target on any normal citizen’s back, he goes bankrupt after regulatory torture. As Franklin Roosevelt’s “brain trust” planned, government is now the “senior partner” of every business, giving every “request” from government officials automatic coercion power. Federal agencies have six ways from Sunday of getting back at a noncompliant company, from the EEOC to the Occupational Safety and Health Administration to the Environmental Protection Agency to Health and Human Services to Securities and Exchange Commission investigations and more. Use an accurate pronoun? Investigation. Hire “one too many” white guys? Investigation. TikTok legislation going through Congress right now would codify federal power to seize social media companies accused of being owned by foreign interests. Shortly after he acquired X, Elon Musk faced a regulatory shakedown costing him tens of millions, and more on the way. He has money like that, but the rest of us don’t. Speech from a private citizen does not have the threat of violence behind it. Speech from a government official, on the other hand, absolutely does and always has. Government officials have powers that other people don’t, and those powers are easily abused, which is exactly why we have a Constitution. SCOTUS needs to take this crucial context into account, making constitutional protections stronger because the government is far, far outside its constitutional bounds. Big tech companies’ very business model depends on government regulators and can be destroyed — or kneecapped — at the stroke of an activist president’s pen. Or, at least, that’s what the president said when Facebook and Twitter didn’t do what he wanted: Section 230 should “immediately be revoked.” This is a president who claims the executive power to unilaterally rewrite laws, ignore laws, and ignore Supreme Court decisions. It’s a president who issues orders as press releases so they go into effect months before they can even begin to be challenged in court. Constitutionally Protected Speech Isn’t Terrorism If justices buy the administration’s nice-guy pretenses of “concern about terrorism,” and “once in a lifetime pandemic measures,” they didn’t read the briefs in this case and see that is simply a cover for the U.S. government turning counterterrorism tools on its own citizens in an attempt to control election outcomes. This is precisely what the First Amendment was designed to check, and we Americans need our Supreme Court to understand that and act to protect us. Elections mean nothing when the government is secretly keeping voters from talking to each other. The Supreme Court may not be able to return the country to full constitutional government by eradicating the almost entirely unconstitutional administrative state. But it should enforce as many constitutional boundaries as possible on such agencies. That clearly includes prohibiting all of government from outsourcing to allegedly “private” organizations actions that would be illegal for the government to take. That includes not just coercive instructions to social media companies, but also developing social media censorship tools and organizations as cutouts for the rogue security state that is targeting peaceful citizens instead of actual terrorists. Even false speech is not domestic terrorism, and no clearheaded Supreme Court justice looking at the evidence could let the Biden administration weaponize antiterrorism measures to strip law-abiding Americans of our fundamental human rights. Joy Pullmann is executive editor of The Federalist, a happy wife, and the mother of six children. Her ebooks include "Classic Books For Young Children," and "101 Strategies For Living Well Amid Inflation." An 18-year education and politics reporter, Joy has testified before nearly two dozen legislatures on education policy and appeared on major media from Fox News to Ben Shapiro to Dennis Prager. Joy is a grateful graduate of the Hillsdale College honors and journalism programs who identifies as native American and gender natural. Her traditionally published books include "The Education Invasion: How Common Core Fights Parents for Control of American Kids," from Encounter Books. https://thefederalist.com/2024/03/21/this-country-cannot-afford-a-weak-supreme-court-decision-on-internet-censorship/ Join ➡️ @MartinKulldorf
    THEFEDERALIST.COM
    This Country Can't Afford A SCOTUS Weak On Internet Censorship
    It is obviously un-American for the government to develop a 'hit list' of citizens to mute through secret pressure on tech monopolies.
    1 Σχόλια 0 Μοιράστηκε 2813 Views
  • 💥💥💥WE all know that mainstream media has been CONTROLLED by the deep state for decades..it's how the levels of LIES and DECEPTION were accepted by so many.....I do still pay attention to mainstream because I choose to know what the "masses" are being fed...I believe we have been watching a lot of "REVERSE Operation Mockingbird" over the last few years...slowly leaking TRUTH for folks to digest...just my opinion 🤷‍♀️ That said, last night IMHO was a HUGE WIN for We the People! 😊 Regardless if you LIke FOX - Dislike FOX - Like Jesse- Dislike Jesse- the fact remains that last night March 19, 2024 at 8pm the TRUTH about Operation Mockingbird and the "Deep State" was being put out on Jesse Watters Primetime...including video clips we have been sharing for years on Telegram and other social media platforms....For me, it's more validation that the Storm IS upon us.... https://www.foxnews.com/video/6349280028112
    💥💥💥WE all know that mainstream media has been CONTROLLED by the deep state for decades..it's how the levels of LIES and DECEPTION were accepted by so many.....I do still pay attention to mainstream because I choose to know what the "masses" are being fed...I believe we have been watching a lot of "REVERSE Operation Mockingbird" over the last few years...slowly leaking TRUTH for folks to digest...just my opinion 🤷‍♀️ That said, last night IMHO was a HUGE WIN for We the People! 😊 Regardless if you LIke FOX - Dislike FOX - Like Jesse- Dislike Jesse- the fact remains that last night March 19, 2024 at 8pm the TRUTH about Operation Mockingbird and the "Deep State" was being put out on Jesse Watters Primetime...including video clips we have been sharing for years on Telegram and other social media platforms....For me, it's more validation that the Storm IS upon us.... https://www.foxnews.com/video/6349280028112
    WWW.FOXNEWS.COM
    Jesse Watters: The 'deep state' is preparing for war | Fox News Video
    Fox News host Jesse Watters gives his take on how the term ‘deep state’ has changed throughout the years on ‘Jesse Watters Primetime.’
    0 Σχόλια 0 Μοιράστηκε 493 Views
  • AltSignals (ASI) outlook amid expert’s “huge” Bitcoin (BTC) prediction

    AltSignals (ASI) recently listed on crypto DEX platform Uniswap.
    Analysts have shared major predictions for Bitcoin (BTC) as price hovers near $51k.
    As Bitcoin bulls struggle to hold prices above $51k, a crypto analyst has shared a potential bearish flip that could see BTC price trade to $48k. Here’s the price outlook for AltSignals.

    BTC price to $48k? Analyst points to on-chain metric
    Bitcoin price rose to above $53k on February 20, hitting the highest level since December 2021. While the bellwether cryptocurrency’s market cap remains above the $1 trillion mark hit this month, prices have revisited the $50.6k level on multiple occasions.

    A crypto analyst has shared a Bitcoin price prediction suggesting BTC could dip to lows of $48k. On-chain and data analytics platform CryptoQuant shared the analyst’s view on X on Monday.

    Per the prediction, the 30-day moving average of Bitcoin’s short term Holder SORP metric shows it’s near the selling zone for short-term investors. The technical chart also shows BTC trading below the resistance, with a breakdown likely to push prices to the $48k area.

    On the other hand, crypto analyst Ali says Bitcoin could retest the $53k level and target $60.5k amid its megaphone pattern formed on the daily chart.

    What could this mean for the altcoin market, for AltSignals price? Largely, declines for Bitcoin have seen the broader market react lower.

    Likewise, a mega rally has often injected new upside momentum in altcoins, likely to be led by ETH as spot Ethereum ETF excitement builds up. A recent report showed 84% of crypto investors see Bitcoin hitting a new all-time high in 2024.

    AltSignals: Trading signals enhanced by AI
    AltSignals has consistently returned win rates averaging 64%. Traders have benefitted from thousands of signals across stocks, crypto and forex among other markets.

    With business on the upside since its debut in 2017, this trading signals platform is now getting ready for the next chapter of growth. It seeks to capitalize on the Artificial Intelligence (AI) boom by integrating a new AI stack dubbed ActualizeAI.

    The platform aims to increase its algorithm’s average win rate from 64% to over 80%.

    Elsewhere, the AltSignals roadmap includes the licensing of ActualizeAI and launch of Actualize Pass NFT marketplace. There are also plans to partner with other platforms to enhance adoption.

    The native token is ASI, which offers holders access to the AI ecosystem.

    AltSignals price prediction: Will ASI token explode 2024?
    The ASI token recently listed on the decentralized exchange (DEX) platform Uniswap, having successfully navigated its presale that closed in December last year.

    As the AI narrative strengthens and crypto markets expand, AltSignals (ASI) looks primed to be one of the top investing opportunities in the market. In the short term, a dip across the market may see ASI token struggle too.

    If the market rallies as anticipated amid Bitcoin’s halving and other tailwinds, the value of ASI could rise significantly. The potential for the AltSignals’ price to 100x is there given the likely demand for ActualizeAI.
    https://token.altsignals.io/
    AltSignals (ASI) outlook amid expert’s “huge” Bitcoin (BTC) prediction AltSignals (ASI) recently listed on crypto DEX platform Uniswap. Analysts have shared major predictions for Bitcoin (BTC) as price hovers near $51k. As Bitcoin bulls struggle to hold prices above $51k, a crypto analyst has shared a potential bearish flip that could see BTC price trade to $48k. Here’s the price outlook for AltSignals. BTC price to $48k? Analyst points to on-chain metric Bitcoin price rose to above $53k on February 20, hitting the highest level since December 2021. While the bellwether cryptocurrency’s market cap remains above the $1 trillion mark hit this month, prices have revisited the $50.6k level on multiple occasions. A crypto analyst has shared a Bitcoin price prediction suggesting BTC could dip to lows of $48k. On-chain and data analytics platform CryptoQuant shared the analyst’s view on X on Monday. Per the prediction, the 30-day moving average of Bitcoin’s short term Holder SORP metric shows it’s near the selling zone for short-term investors. The technical chart also shows BTC trading below the resistance, with a breakdown likely to push prices to the $48k area. On the other hand, crypto analyst Ali says Bitcoin could retest the $53k level and target $60.5k amid its megaphone pattern formed on the daily chart. What could this mean for the altcoin market, for AltSignals price? Largely, declines for Bitcoin have seen the broader market react lower. Likewise, a mega rally has often injected new upside momentum in altcoins, likely to be led by ETH as spot Ethereum ETF excitement builds up. A recent report showed 84% of crypto investors see Bitcoin hitting a new all-time high in 2024. AltSignals: Trading signals enhanced by AI AltSignals has consistently returned win rates averaging 64%. Traders have benefitted from thousands of signals across stocks, crypto and forex among other markets. With business on the upside since its debut in 2017, this trading signals platform is now getting ready for the next chapter of growth. It seeks to capitalize on the Artificial Intelligence (AI) boom by integrating a new AI stack dubbed ActualizeAI. The platform aims to increase its algorithm’s average win rate from 64% to over 80%. Elsewhere, the AltSignals roadmap includes the licensing of ActualizeAI and launch of Actualize Pass NFT marketplace. There are also plans to partner with other platforms to enhance adoption. The native token is ASI, which offers holders access to the AI ecosystem. AltSignals price prediction: Will ASI token explode 2024? The ASI token recently listed on the decentralized exchange (DEX) platform Uniswap, having successfully navigated its presale that closed in December last year. As the AI narrative strengthens and crypto markets expand, AltSignals (ASI) looks primed to be one of the top investing opportunities in the market. In the short term, a dip across the market may see ASI token struggle too. If the market rallies as anticipated amid Bitcoin’s halving and other tailwinds, the value of ASI could rise significantly. The potential for the AltSignals’ price to 100x is there given the likely demand for ActualizeAI. https://token.altsignals.io/
    TOKEN.ALTSIGNALS.IO
    AltSignals Presale - Invest In The AI Revolution With The ASI Token
    Become a part of AltSignals new AI development ActualizeAI, and join the fastest growing AI project in crypt
    Like
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    0 Σχόλια 0 Μοιράστηκε 7196 Views
  • Best Freelancing Sites
    When it comes to freelancing, the digital landscape offers a myriad of platforms where you can showcase your skills and land exciting gigs. Here are some of the best freelancing sites that cater to a wide range of talents:

    Upwork: Think of Upwork as the bustling marketplace of freelancing. With millions of jobs posted annually across various categories like writing, design, programming, and virtual assistance, there's something for everyone here.

    Fiverr: Fiverr's unique approach allows freelancers to offer "gigs" or services starting at $5, covering everything from graphic design and copywriting to voiceovers and digital marketing.
    Read Details: https://shorturl.at/zACV3
    Best Freelancing Sites When it comes to freelancing, the digital landscape offers a myriad of platforms where you can showcase your skills and land exciting gigs. Here are some of the best freelancing sites that cater to a wide range of talents: Upwork: Think of Upwork as the bustling marketplace of freelancing. With millions of jobs posted annually across various categories like writing, design, programming, and virtual assistance, there's something for everyone here. Fiverr: Fiverr's unique approach allows freelancers to offer "gigs" or services starting at $5, covering everything from graphic design and copywriting to voiceovers and digital marketing. Read Details: https://shorturl.at/zACV3
    Best Freelancing site
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    0 Σχόλια 0 Μοιράστηκε 2650 Views
  • Showcase a full-fledged social media plan that define the target audiences, competitors, company USP, roadblocks and vision using this fully editable one page social media plan PowerPoint template. You can use this PPT template to understand the audiences behaviour in different social media platforms and their analytics.
    Watch Now: https://youtube.com/shorts/PzHB0-Dwsls
    Download Now: https://bit.ly/3Ho9907
    #socialmediaplan #SocialMediaMarketing #OnePage #powerpointpresentation #slides
    Showcase a full-fledged social media plan that define the target audiences, competitors, company USP, roadblocks and vision using this fully editable one page social media plan PowerPoint template. You can use this PPT template to understand the audiences behaviour in different social media platforms and their analytics. Watch Now: https://youtube.com/shorts/PzHB0-Dwsls Download Now: https://bit.ly/3Ho9907 #socialmediaplan #SocialMediaMarketing #OnePage #powerpointpresentation #slides
    0 Σχόλια 0 Μοιράστηκε 3278 Views

  • The Ultimate Guide to $750 Cash App Gift Card Rewards Store 2024

    In the era of digital rewards and cash incentives, the allure of gift cards has become increasingly prominent. Among the plethora of options available, the $750 Cash App Gift Card stands out as a lucrative and versatile reward, offering recipients the flexibility to choose how they wish to utilize their earnings. Whether you're aiming to treat yourself or seeking the perfect gift for a loved one, understanding the intricacies of this rewards store is essential to maximizing its benefits. Here's everything you need to know about the $750 Cash App Gift Card Rewards Store in 2024:

    Diverse Redemption Options:

    One of the most enticing aspects of the $750 Cash App Gift Card Rewards Store is its wide range of redemption options. From popular retailers and online marketplaces to subscription services and entertainment platforms, recipients have the freedom to explore an extensive selection of products and experiences. Whether you're in need of household essentials, craving a shopping spree, or looking to indulge in streaming services, the $750 Cash App Gift Card ensures that there's something for everyone.

    Seamless Integration with Cash App:

    As a prominent player in the realm of digital finance, Cash App offers users a seamless and convenient experience when it comes to managing their funds. The integration of the $750 Gift Card into the Cash App ecosystem further enhances this convenience, allowing recipients to effortlessly redeem their rewards and track their transactions within a single platform. With intuitive features and user-friendly interfaces, navigating the rewards store becomes a hassle-free experience for users of all backgrounds.

    Enhanced Security Measures:

    Security is paramount in today's digital landscape, and the $750 Cash App Gift Card Rewards Store prioritizes the safety and privacy of its users. Robust encryption protocols and stringent authentication measures safeguard sensitive information, ensuring that transactions remain secure and protected against potential threats. Whether you're redeeming your rewards online or making in-store purchases, you can rest assured that your personal and financial data are in safe hands.

    Exclusive Deals and Promotions:

    In addition to its diverse redemption options, the $750 Cash App Gift Card Rewards Store offers exclusive deals and promotions to enhance the value proposition for its users. From limited-time discounts to special offers on premium products and services, there are ample opportunities to stretch your rewards further and make the most out of your shopping experience. Keep an eye out for notifications and updates to capitalize on these lucrative deals and maximize your savings.

    User-Friendly Redemption Process:

    Navigating the $750 Cash App Gift Card Rewards Store is a breeze, thanks to its intuitive redemption process. Whether you prefer to browse through categories or search for specific items, the platform offers a seamless and user-friendly interface that caters to your preferences. With just a few clicks or taps, you can select your desired rewards, complete your transaction, and enjoy the satisfaction of securing valuable products or experiences with your gift card earnings.

    conclusion, the $750 Cash App Gift Card Rewards Store represents a compelling opportunity for individuals seeking versatile and rewarding experiences in 2024. With its diverse redemption options, seamless integration with Cash App, enhanced security measures, exclusive deals, and user-friendly redemption process, it's no wonder why this rewards store continues to captivate users worldwide. Whether you're treating yourself or surprising a loved one, the $750 Cash App Gift Card is your ticket to unlocking a world of possibilities and indulging in the rewards you deserve.
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    The Ultimate Guide to $750 Cash App Gift Card Rewards Store 2024 In the era of digital rewards and cash incentives, the allure of gift cards has become increasingly prominent. Among the plethora of options available, the $750 Cash App Gift Card stands out as a lucrative and versatile reward, offering recipients the flexibility to choose how they wish to utilize their earnings. Whether you're aiming to treat yourself or seeking the perfect gift for a loved one, understanding the intricacies of this rewards store is essential to maximizing its benefits. Here's everything you need to know about the $750 Cash App Gift Card Rewards Store in 2024: Diverse Redemption Options: One of the most enticing aspects of the $750 Cash App Gift Card Rewards Store is its wide range of redemption options. From popular retailers and online marketplaces to subscription services and entertainment platforms, recipients have the freedom to explore an extensive selection of products and experiences. Whether you're in need of household essentials, craving a shopping spree, or looking to indulge in streaming services, the $750 Cash App Gift Card ensures that there's something for everyone. Seamless Integration with Cash App: As a prominent player in the realm of digital finance, Cash App offers users a seamless and convenient experience when it comes to managing their funds. The integration of the $750 Gift Card into the Cash App ecosystem further enhances this convenience, allowing recipients to effortlessly redeem their rewards and track their transactions within a single platform. With intuitive features and user-friendly interfaces, navigating the rewards store becomes a hassle-free experience for users of all backgrounds. Enhanced Security Measures: Security is paramount in today's digital landscape, and the $750 Cash App Gift Card Rewards Store prioritizes the safety and privacy of its users. Robust encryption protocols and stringent authentication measures safeguard sensitive information, ensuring that transactions remain secure and protected against potential threats. Whether you're redeeming your rewards online or making in-store purchases, you can rest assured that your personal and financial data are in safe hands. Exclusive Deals and Promotions: In addition to its diverse redemption options, the $750 Cash App Gift Card Rewards Store offers exclusive deals and promotions to enhance the value proposition for its users. From limited-time discounts to special offers on premium products and services, there are ample opportunities to stretch your rewards further and make the most out of your shopping experience. Keep an eye out for notifications and updates to capitalize on these lucrative deals and maximize your savings. User-Friendly Redemption Process: Navigating the $750 Cash App Gift Card Rewards Store is a breeze, thanks to its intuitive redemption process. Whether you prefer to browse through categories or search for specific items, the platform offers a seamless and user-friendly interface that caters to your preferences. With just a few clicks or taps, you can select your desired rewards, complete your transaction, and enjoy the satisfaction of securing valuable products or experiences with your gift card earnings. conclusion, the $750 Cash App Gift Card Rewards Store represents a compelling opportunity for individuals seeking versatile and rewarding experiences in 2024. With its diverse redemption options, seamless integration with Cash App, enhanced security measures, exclusive deals, and user-friendly redemption process, it's no wonder why this rewards store continues to captivate users worldwide. Whether you're treating yourself or surprising a loved one, the $750 Cash App Gift Card is your ticket to unlocking a world of possibilities and indulging in the rewards you deserve. check site: https://sites.google.com/view/clickherecahha/home
    0 Σχόλια 0 Μοιράστηκε 9369 Views
  • Singapore Police investigate two events amid Israel’s genocide in Gaza
    Singapore Police Force in a statement said it is probing two events on 2 Feb for Public Order Act breaches, urging lawful, respectful dialogue on Israel-Hamas conflict as death toll in the Gaza Strip has surpassed 28,000, with more than 67,600 Palestinians wounded.

    Staff writer13 February 2024

    SINGAPORE: The Singapore Police Force (SPF) is currently investigating two events held on 2 February that may have breached the Public Order Act amidst the ongoing Israel-Hamas conflict and genocide in Gaza.

    In their statement on Tuesday (13 Feb), the SPF also emphasized the importance of maintaining respectful and responsible discussions concerning the conflict, highlighting the illegal nature of participating in public protests without the requisite permit.

    The first event under investigation saw approximately 70 individuals congregating along Orchard Road, proceeding towards the Istana with umbrellas adorned with watermelon imagery—a recognized symbol of Palestinian resistance.

    This march, potentially advocating for the political causes of other countries, has raised concerns over stirring tensions and leading to public disorder, particularly given the security sensitivity of the Istana area.

    A second incident involved a private gathering which was captured and shared online where a subject was seen live streaming publicly and chanting, “From the river to the sea”, and others chanting “, Palestine will be free”, in response.

    The participants in the private event called for stopping the purchase of Israeli arms, ending Singaporean partnerships with Israeli institutions, halting all diplomatic relations with Israel, ceasing participation in the US-led attacks in the Red Sea, and stopping police investigations into peaceful expressions of support for Palestine.

    SPF states, “The phrase “From the river to the sea” is associated with calls for the destruction of the State of Israel. The use of such phrases can lead to racial tensions in our society, and may be an offence under Section 298A(a) of the Penal Code 1871. We must also not condone calls for violence.”

    The participants in the private event, made calls for the Singapore government

    Reflecting on these incidents, the SPF reiterated its stance from October 2023, alongside the National Parks Board, that applications for public events related to the Israel-Hamas conflict would be systematically rejected due to public safety and security concerns.

    The SPF’s statement further stressed the importance of not allowing international events to disrupt Singapore’s internal harmony, pointing out the “real risk” assemblies related to the Gaza situation pose to public order and inter-community relations.

    In line with this, the SPF has made it clear that no permits will be granted for gatherings that risk inciting disorder or advocate for foreign political causes.

    Additionally, SPF noted that unauthorized posting of materials such as stickers on properties remains a punishable offence under the Miscellaneous Offences (Public Order and Nuisance) Act.

    In a supportive stance, Josephine Teo, Minister for Communications and Information and Second Minister for the Ministry of Home Affairs, echoed the police’s sentiments in a Facebook post.

    She reassured that the advisory is not aimed at stifling expression but rather at ensuring that public discourse does not infringe upon the law or threaten societal cohesion.

    Minister Teo also highlighted Singapore’s proactive stance on the conflict, noting the country’s contribution to humanitarian efforts and its call for an immediate ceasefire through international platforms.

    The death toll in the Gaza Strip has surpassed 28,000, with more than 67,600 Palestinians wounded since the Israeli offensive on Gaza began on 7 October last year.

    On 26 January, the International Court of Justice ordered Israel to limit deaths and damage but stopped short of demanding a cease-fire in the Palestinian territory.

    South Africa has accused Israel of genocide and requested the World Court in The Hague, Netherlands, to impose interim measures as the case proceeds. These requested measures include ordering Israel to halt its offensive, allowing Gaza residents access to aid, and taking “reasonable measures” to prevent genocide.

    Israel has denied committing genocide and asked the court to dismiss the case, which the panel of 17 judges refused to do.

    Casualties in Gaza are expected to increase as Israeli Prime Minister Benjamin Netanyahu calls for a ground invasion of Rafah, where 1.4 million civilians are crammed into the city, trapped between Isreal’s offensive in the north and Egypt’s border where it has been said that it would not allow passage.

    Gutzy has checked with the organisers of the events and understands that they have yet to be contacted by the police and that the President has yet respond to the letters that were sent on 2 February.


    Singapore Police Force in a statement said it is probing two events on 2 Feb for Public Order Act breaches, urging lawful, respectful dialogue on Israel-Hamas conflict as death toll in the Gaza Strip has surpassed 28,000, with more than 67,600 Palestinians wounded.




    https://gutzy.asia/2024/02/13/singapore-police-investigate-two-events-amid-israels-genocide-in-gaza/

    https://donshafi911.blogspot.com/2024/02/singapore-police-investigate-two-events.html
    Singapore Police investigate two events amid Israel’s genocide in Gaza Singapore Police Force in a statement said it is probing two events on 2 Feb for Public Order Act breaches, urging lawful, respectful dialogue on Israel-Hamas conflict as death toll in the Gaza Strip has surpassed 28,000, with more than 67,600 Palestinians wounded. Staff writer13 February 2024 SINGAPORE: The Singapore Police Force (SPF) is currently investigating two events held on 2 February that may have breached the Public Order Act amidst the ongoing Israel-Hamas conflict and genocide in Gaza. In their statement on Tuesday (13 Feb), the SPF also emphasized the importance of maintaining respectful and responsible discussions concerning the conflict, highlighting the illegal nature of participating in public protests without the requisite permit. The first event under investigation saw approximately 70 individuals congregating along Orchard Road, proceeding towards the Istana with umbrellas adorned with watermelon imagery—a recognized symbol of Palestinian resistance. This march, potentially advocating for the political causes of other countries, has raised concerns over stirring tensions and leading to public disorder, particularly given the security sensitivity of the Istana area. A second incident involved a private gathering which was captured and shared online where a subject was seen live streaming publicly and chanting, “From the river to the sea”, and others chanting “, Palestine will be free”, in response. The participants in the private event called for stopping the purchase of Israeli arms, ending Singaporean partnerships with Israeli institutions, halting all diplomatic relations with Israel, ceasing participation in the US-led attacks in the Red Sea, and stopping police investigations into peaceful expressions of support for Palestine. SPF states, “The phrase “From the river to the sea” is associated with calls for the destruction of the State of Israel. The use of such phrases can lead to racial tensions in our society, and may be an offence under Section 298A(a) of the Penal Code 1871. We must also not condone calls for violence.” The participants in the private event, made calls for the Singapore government Reflecting on these incidents, the SPF reiterated its stance from October 2023, alongside the National Parks Board, that applications for public events related to the Israel-Hamas conflict would be systematically rejected due to public safety and security concerns. The SPF’s statement further stressed the importance of not allowing international events to disrupt Singapore’s internal harmony, pointing out the “real risk” assemblies related to the Gaza situation pose to public order and inter-community relations. In line with this, the SPF has made it clear that no permits will be granted for gatherings that risk inciting disorder or advocate for foreign political causes. Additionally, SPF noted that unauthorized posting of materials such as stickers on properties remains a punishable offence under the Miscellaneous Offences (Public Order and Nuisance) Act. In a supportive stance, Josephine Teo, Minister for Communications and Information and Second Minister for the Ministry of Home Affairs, echoed the police’s sentiments in a Facebook post. She reassured that the advisory is not aimed at stifling expression but rather at ensuring that public discourse does not infringe upon the law or threaten societal cohesion. Minister Teo also highlighted Singapore’s proactive stance on the conflict, noting the country’s contribution to humanitarian efforts and its call for an immediate ceasefire through international platforms. The death toll in the Gaza Strip has surpassed 28,000, with more than 67,600 Palestinians wounded since the Israeli offensive on Gaza began on 7 October last year. On 26 January, the International Court of Justice ordered Israel to limit deaths and damage but stopped short of demanding a cease-fire in the Palestinian territory. South Africa has accused Israel of genocide and requested the World Court in The Hague, Netherlands, to impose interim measures as the case proceeds. These requested measures include ordering Israel to halt its offensive, allowing Gaza residents access to aid, and taking “reasonable measures” to prevent genocide. Israel has denied committing genocide and asked the court to dismiss the case, which the panel of 17 judges refused to do. Casualties in Gaza are expected to increase as Israeli Prime Minister Benjamin Netanyahu calls for a ground invasion of Rafah, where 1.4 million civilians are crammed into the city, trapped between Isreal’s offensive in the north and Egypt’s border where it has been said that it would not allow passage. Gutzy has checked with the organisers of the events and understands that they have yet to be contacted by the police and that the President has yet respond to the letters that were sent on 2 February. Singapore Police Force in a statement said it is probing two events on 2 Feb for Public Order Act breaches, urging lawful, respectful dialogue on Israel-Hamas conflict as death toll in the Gaza Strip has surpassed 28,000, with more than 67,600 Palestinians wounded. https://gutzy.asia/2024/02/13/singapore-police-investigate-two-events-amid-israels-genocide-in-gaza/ https://donshafi911.blogspot.com/2024/02/singapore-police-investigate-two-events.html
    GUTZY.ASIA
    Singapore Police investigate two events amid Israel’s genocide in Gaza
    Singapore Police Force in a statement said it is probing two events on 2 Feb for Public Order Act breaches, urging lawful, respectful dialogue on Israel-Hamas conflict as death toll in the Gaza Strip has surpassed 28,000, with more than 67,600 Palestinians wounded.
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  • The dark web: a journey into the dark sides of the internet

    The internet represents a large and complex aspect of human daily life, where information is exchanged and social interaction takes place in an unprecedented way. However, there is a small and dark part of the internet known as the dark web, which intrigues some and terrifies others.

    The dark web is a part of the internet that remains hidden from traditional search engines and requires special technologies to access it, such as using the Tor private network (TOR). This dark side of the internet allows users to access sites and services for the exchange of information and goods in illegal or unethical ways.

    Activities on the dark web are very diverse, as individuals can find sites for drug trafficking, selling weapons, exchanging confidential information, and even ordering electronic hacking services. In addition, there are also platforms for illegal file sharing and circulation of extremist ideas.

    With such a wide variety, the dark web raises big questions about privacy and security on the internet. Can States and authorities effectively combat this dark side How can individuals protect themselves from potential dangers

    However, it is worth noting that the dark web is not necessarily a completely dangerous place, as there are also activities there aimed at maintaining privacy and moving in the dark without it being harmful. Bloggers and journalists can sometimes use the dark web to share information confidentially and securely.

    In the end, the dark web remains a controversial part of the internet, combining opportunities and challenges. Interaction with this dark world requires caution and awareness, as drifting into it can be dangerous and expose individuals to many dangers.
    The dark web: a journey into the dark sides of the internet The internet represents a large and complex aspect of human daily life, where information is exchanged and social interaction takes place in an unprecedented way. However, there is a small and dark part of the internet known as the dark web, which intrigues some and terrifies others. The dark web is a part of the internet that remains hidden from traditional search engines and requires special technologies to access it, such as using the Tor private network (TOR). This dark side of the internet allows users to access sites and services for the exchange of information and goods in illegal or unethical ways. Activities on the dark web are very diverse, as individuals can find sites for drug trafficking, selling weapons, exchanging confidential information, and even ordering electronic hacking services. In addition, there are also platforms for illegal file sharing and circulation of extremist ideas. With such a wide variety, the dark web raises big questions about privacy and security on the internet. Can States and authorities effectively combat this dark side How can individuals protect themselves from potential dangers However, it is worth noting that the dark web is not necessarily a completely dangerous place, as there are also activities there aimed at maintaining privacy and moving in the dark without it being harmful. Bloggers and journalists can sometimes use the dark web to share information confidentially and securely. In the end, the dark web remains a controversial part of the internet, combining opportunities and challenges. Interaction with this dark world requires caution and awareness, as drifting into it can be dangerous and expose individuals to many dangers.
    0 Σχόλια 0 Μοιράστηκε 5046 Views
  • Hypothetical “Disease X”: The WHO Pandemic Treaty Is a Fraud. Demands Compliance for “Next Pandemic”
    “Very narrow national interests should not come in the way”

    Michel Chossudovsky
    [This article was originally published by Global Research. Click here to read this article on Global Research.]

    Introduction

    WHO Director General Tedros Adhanom Ghebreyesus continues to mislead public opinion worldwide.

    There is no such thing as “Disease X”. It’s a hypothetical construct by a WHO expert committee (2017-2018) of virologists and disease analysts. It was then envisaged in the Clade X Simulation (May 2018) and Event 201 Simulation of a Pandemic (October 2019). Both events were held under the auspices of the John Hopkins Center for Heath Security with the support of the Gates Foundation.

    It was then announced by Bill Gates at the Munich Security Conference in February 2022:

    “The risks of severe disease from Covid-19 have “dramatically reduced” but another pandemic is all but certain,” says Bill Gates.

    “A potential new pandemic would likely stem from a different pathogen to that of the coronavirus family” (CNBC).

    “We’ll have another pandemic. It will be a different pathogen next time,” Gates said.

    How could he know this in advance?

    “Predicting” and “Preparing” for “Disease X”, an Unknown Threat

    In his presentation at the Davos24 WEF, the WHO Director General Dr. Tedros recanted Bill Gates’s premonition, pointing to the alleged severity of the Covid-19 crisis initiated in early 2020, in blatant contradiction with official WHO data.

    Bill Gates is Tedros’s mentor. They have a close personal relationship, which occasionally borders on “conflict of interest”.

    Bill Gates, Tedros et al. (supported by the WHO “committee of experts”) are now predicting “Disease X” which stems from a hypothetical pathogen which is allegedly 20 times more deadly than SARS-CoV-2. What absolute nonsense.

    “Aside from the fact that it will wreak havoc on humanity, the research team has no idea about the nature of the pathogen.”

    According to Forbes:

    Disease X, a hypothetical unknown threat, is the name used among scientists to encourage the development of countermeasures, including vaccines and tests, to deploy in the case of a future outbreak—the WHO convened a group of over 300 scientists in November 2022 to study the “unknown pathogen that could cause a serious international epidemic,” positing a mortality rate 20 times that of Covid-19″

    300 scientists to study something which is unknown and hypothetical? The media propaganda buzz, quoting “scientific opinion” is “Disease X 20 times more dangerous than Covid.”

    A renewed fear campaign 24/7 has been launched, consisting of reports of an alleged new wave of Covid deaths, while totally ignoring the tide of excess mortality and morbidity resulting from the Covid-19 “vaccine”.

    Video: A Vaccine for a Hypothetical “Disease X” Pandemic.

    Produced by Lux Media. Michel Chossudovsky and Caroline Mailloux


    Click here to watch the interview.

    “Disease X” Alleged Pathogen “Identified” by WHO Expert Committee Two Years Prior to the Covid-19 Crisis

    In early February 2018, a WHO expert committee convened behind closed doors in Geneva “to consider the unthinkable”.

    “The goal was to identify pathogens with the potential to spread and kill millions but for which there are currently no, or insufficient, countermeasures available.”

    The Expert Committee had met on two previous occasions, most probably in 2017:

    “It was the third time the committee, consisting of leading virologists, bacteriologists and infectious disease experts, had met to consider diseases with epidemic or pandemic potential.

    But when the 2018 list was released two weeks ago [mid February 2018] it included an entry not seen in previous years.

    In addition to eight frightening but familiar diseases including Ebola, Zika, and Severe Acute Respiratory Syndrome (SARS), the list included a ninth global threat: Disease X.” (Daily Telegraph, emphasis added)

    It all sounds very scientific based on experts contracted and rewarded by the WHO, under the advice of the Bill and Melinda Gates Foundation:

    “Disease X represents the knowledge [what knowledge?] that a serious international epidemic could be caused by a pathogen currently unknown to cause human disease”.

    Experts on the WHO panel say Disease X could emerge from a variety of sources and strike at any time.

    “History tells us that it is likely the next big outbreak will be something we have not seen before”, said John-Arne Rottingen, chief executive of the Research Council of Norway and a scientific adviser to the WHO committee.

    “It may seem strange to be adding an ‘X’ but the point is to make sure we prepare and plan flexibly in terms of vaccines and diagnostic tests.

    “We want to see ‘plug and play’ platforms developed which will work for any, or a wide number of diseases; systems that will allow us to create countermeasures at speed.” (Telegraph)

    The work of the “expert committee” was followed by two table top simulations respectively in May 2018 and October 2019.

    The Clade X Simulation: “Parainfluenza Clade X”

    A few months following the WHO experts’ meeting in Geneva in early 2018, at which a hypothetical Disease X was categorized as a “global threat’, the Clade X table top simulation was conducted Washington D.C. (May 2018) under the auspices of The Johns Hopkins Center for Health Security.

    “The scenario begins with an outbreak of novel parainfluenza virus that is moderately contagious and moderately lethal and for which there are no effective medical countermeasures”.

    The virus is called: “Parainfluenza Clade X”

    “Disease X” and the 201 Global Pandemic Simulation

    The Hypothetical Disease X Concept developed in 2017-2018 by a WHO Expert Committee of leading virologists and disease experts was simulated in the Event 201 Table Top Simulation of a deadly corona virus pandemic. The Global Pandemic Exercise was held in New York under the auspices of the John Hopkins Bloomberg School of Health, Centre for Heath Security (which hosted the May 2018 Clade X Simulation). The event was sponsored by the Gates Foundation and the World Economic Forum. (Event 201)

    An October 21, 2019 report “Disease X dummy run: World health experts prepare for a deadly pandemic and its fallout confirms that Disease X was part of the 201 Global Pandemic Simulation:

    On Friday a panel of 15 high-powered international figures gathered in the ballroom of a New York hotel to “game” a scenario in which a pandemic is raging across the world, killing millions.

    Health experts fully expect the world to be confronted by a fast-moving global pandemic. The updates were coming into the situation room thick and fast – and the news was not good. The virus was spreading… The former deputy director of the CIA took off her glasses, rubbed her eyes, and addressed the panel. “We also have to consider that terrorists could take advantage of this situation,” she said. “We’re looking at the possibility of famine. There is the potential for outbreaks of secondary diseases.”

    “I fully expect that we will be confronted by a fast-moving global pandemic,” said Dr Mike Ryan, executive director of the World Health Organisation (WHO) health emergencies programme.

    Addressing participants – and the 150 observers – before the scenario began, he said that the WHO deals with 200 epidemics every year. It’s only a matter of time before one of those becomes a pandemic – defined as a disease prevalent over a whole country or the world.” (Telegraph, emphasis added)



    Video: Tedros Stated that Covid was “The First Disease X”


    Click here to watch the video.

    Evidence: No Pandemic in Early 2020. Misleading Statements by Dr. Tedros, Fraudulent Decisions

    In a factual nutshell:

    WHO Director General Dr. Tedros Adhanom Ghebreyesus launched a Public Health Emergency of International Concern (PHEIC) on January 30th 2020. There was 83 “confirmed cases” outside China for a population of 6.4 billion people.

    There was no “scientific basis” to justify the launching of a Worldwide Public Health Emergency.

    On February 20th, 2020: At a briefing in Geneva, the WHO Director General Dr Tedros said that he was “concerned that the chance to contain the coronavirus outbreak was “closing” …“I believe the window of opportunity is still there, but that the window is narrowing.” Those statements were based on 1076 “confirmed cases” outside China.

    The WHO officially declared a Worldwide pandemic on March 11, 2020 at a time when the number of PCR cases outside China (6.4 billion population) was of the order of 44,279 cumulative confirmed cases.

    All so-called confirmed cases are the result of the PCR test, which does not detect the virus.

    In the US on March 9, 2020, there were 3,457 “confirmed cases” out of a population of 329.5 million people.

    In Canada on March 9, 2020, there were 125 “confirmed cases” out of a population of 38.5 million people.

    In Germany on March 9, 2020, there were 2948 “confirmed cases” out of a population of 83.2 million people.

    The above is a summary. Click here and scroll down for references and analysis.

    The “Disease X” Fear Campaign and the Pandemic Treaty

    There is vast literature on the Pandemic Treaty and its likely consequences.

    The Pandemic Treaty consists in creating a global health entity under WHO auspices. It’s the avenue towards “Global Governance” whereby the entire world population of 8 billion would be digitized, integrated into a global digital data bank.

    All your personal information would be contained in this data bank, leading to the derogation of fundamental human rights as well as the subordination of national governments to dominant financial establishment.

    The Pandemic Treaty would be tied into the creation of a worldwide digital ID system.

    According to David Skripac:

    “A worldwide digital ID system is in the making. [The aim] of the WEF—and of all the central banks [is] to implement a global system in which everyone’s personal data will be incorporated into the Central Bank Digital Currency (CBDC) network.”

    Peter Koenig describes the underlying process as:

    “an all-electronic ID – linking everything to everything of each individual (records of health, banking, personal and private, etc.).”

    Bombshell: A Vaccine for a Hypothetical “Disease X” Pandemic “with an Unknown Pathogen”

    Announced by Dr. Tedros at Davos24, not to mention Bill Gates’s numerous authoritative statements, governments must prepare for the outbreak of “Disease X”.

    A State of the Art “Vaccine” allegedly to “Build our Immunity” against “Disease X” (which is a hypothetical construct based on an unknown pathogen) is slated to be developed at Britain’s “Vaccine Development and Evaluation Centre” (UK Health and Security Agency’s (UKHSA) Porton Down campus in Wiltshire, inaugurated in August 2023.

    “Ministers have opened a new vaccine research centre in the UK where scientists will work on preparing for “disease X”, the next potential pandemic pathogen.

    Prof Dame Jenny Harries said: “What we’re trying to do now is capture that really excellent work from Covid and make sure we’re using that as we go forward for any new pandemic threats.”

    She added: “What we try to do here is keep an eye on the ones that we do know. For example, with Covid, we are still here testing all the new variants with the vaccines that have been provided to check they are still effective.

    “But we are also looking at how quickly we can develop a new test that would be used if a brand new virus popped up somewhere.” …

    “This state-of-the-art complex will also help us deliver on our commitment to produce new vaccines within 100 days of a new threat being identified.”

    (The Guardian, emphasis added)

    The “Disease X” “Vaccine” Is to be Developed at the U.K. Ministry of Defense Science and Technology Porter Down Campus

    “The Vaccine Development and Evaluation Centre” (VDEC) –which has a mandate to develop “The Disease X” Vaccine– is a civilian research entity under Britain’s National Health Service (NHS) managed by the UK Health and Security Agency (UKHSA) headed by Dame Jennifer Harries (DBE).

    Of significance VDEC which was inaugurated in August 2023 is located in:

    The “Defence Science and Technology Laboratory” [Dstl] at Porton Down, Wiltshire, which is one of the U.K.’s Ministry of Defense’s most secretive and controversial military research facilities specializing in the testing of biological and chemical weapons.

    The UK Health and Security Agency (UKHSA) has initiated a project in global and country-level “Integrated Disease Surveillance” funded by the Bill and Melinda Gates Foundation. A representative of the Gates Foundation is a member of UKHSA’s Advisory Board.

    What is required is a mass movement to oppose the adoption of the Pandemic Treaty at the World Health Assembly (May 27, 2024).

    We also call for the immediate cancellation of the Covid-19 “Killer Vaccine.”

    Ironically to say the least, the WHO Director General Tedros admits that

    “the momentum had been slowed down by entrenched positions and “a torrent of fake news, lies, and conspiracy theories”.

    Click here to read Steve Watson’s article titled World Health Organisation Head: Global Compliance Needed For Next Pandemic.


    https://open.substack.com/pub/michelchossudovsky/p/hypothetical-disease-x-who-pandemic-treaty-fraud

    It is surely obvious to any dispassionate observer that this coalition of the powerful intends to spring some health crisis upon the people of the world.

    When have the rich and powerful given a care about the health of poor people? That’ll be never.

    Pandemics are not a thing. Think back through your life. How many pandemics have there been? Covid wasn’t one. The Spanish flu nonsense wasn’t one. None of the flu like illnesses reported in the 1960s were one. I don’t believe there has ever been even one.

    Scary infectious diseases are only scary until you stumble across medical research literature going back as far a century and more, in which numerous, serious clinical research studies were set up to detect and measure symptomatic transmission (causing a well person to fall ill with similar symptoms to those of the donor person). Try as they might, that didn’t happen. Contagion in this specific scenario (acute respiratory diseases) does not happen.

    So when they come at you with the next bunch of lies, try to spot the lies as the mealy mouthed, wet, TV presenters talk nonsense!

    Then to this “100 day vaccine” idiocy. As you really going to roll your sleeve up and receive an injection of mRNA wrapped in lipid nanoparticles? They will be toxic.

    Do note that Porton Down, the government’s own formerly named Chemical Defence Establishment, has been tapped as the people to do it! Wouldn’t you want to work with the people who claimed to have whipped up by far the world record speed of vaccine R&D & product delivery? They cut down the time needed by 90%. Surely you’d give the task to those people? So they’re giving it to a military group who haven’t ever done anything like this before?

    You don’t need a vaccine. Even if everything else was true, it’s out of the question to rustle up a jab in 100 days. Impossible to do it in under several yearrs which, by the way, is FAR FAR longer than the length of time that it’s claimed for the longest lasting pandemic, ever.

    I hope this helps you to respond appropriately, before the next nonsense arrives!

    Best wishes
    Mike

    👉 https://t.me/DrMikeYeadon

    https://donshafi911.blogspot.com/2024/02/hypothetical-disease-x-who-pandemic.html
    Hypothetical “Disease X”: The WHO Pandemic Treaty Is a Fraud. Demands Compliance for “Next Pandemic” “Very narrow national interests should not come in the way” Michel Chossudovsky [This article was originally published by Global Research. Click here to read this article on Global Research.] Introduction WHO Director General Tedros Adhanom Ghebreyesus continues to mislead public opinion worldwide. There is no such thing as “Disease X”. It’s a hypothetical construct by a WHO expert committee (2017-2018) of virologists and disease analysts. It was then envisaged in the Clade X Simulation (May 2018) and Event 201 Simulation of a Pandemic (October 2019). Both events were held under the auspices of the John Hopkins Center for Heath Security with the support of the Gates Foundation. It was then announced by Bill Gates at the Munich Security Conference in February 2022: “The risks of severe disease from Covid-19 have “dramatically reduced” but another pandemic is all but certain,” says Bill Gates. “A potential new pandemic would likely stem from a different pathogen to that of the coronavirus family” (CNBC). “We’ll have another pandemic. It will be a different pathogen next time,” Gates said. How could he know this in advance? “Predicting” and “Preparing” for “Disease X”, an Unknown Threat In his presentation at the Davos24 WEF, the WHO Director General Dr. Tedros recanted Bill Gates’s premonition, pointing to the alleged severity of the Covid-19 crisis initiated in early 2020, in blatant contradiction with official WHO data. Bill Gates is Tedros’s mentor. They have a close personal relationship, which occasionally borders on “conflict of interest”. Bill Gates, Tedros et al. (supported by the WHO “committee of experts”) are now predicting “Disease X” which stems from a hypothetical pathogen which is allegedly 20 times more deadly than SARS-CoV-2. What absolute nonsense. “Aside from the fact that it will wreak havoc on humanity, the research team has no idea about the nature of the pathogen.” According to Forbes: Disease X, a hypothetical unknown threat, is the name used among scientists to encourage the development of countermeasures, including vaccines and tests, to deploy in the case of a future outbreak—the WHO convened a group of over 300 scientists in November 2022 to study the “unknown pathogen that could cause a serious international epidemic,” positing a mortality rate 20 times that of Covid-19″ 300 scientists to study something which is unknown and hypothetical? The media propaganda buzz, quoting “scientific opinion” is “Disease X 20 times more dangerous than Covid.” A renewed fear campaign 24/7 has been launched, consisting of reports of an alleged new wave of Covid deaths, while totally ignoring the tide of excess mortality and morbidity resulting from the Covid-19 “vaccine”. Video: A Vaccine for a Hypothetical “Disease X” Pandemic. Produced by Lux Media. Michel Chossudovsky and Caroline Mailloux Click here to watch the interview. “Disease X” Alleged Pathogen “Identified” by WHO Expert Committee Two Years Prior to the Covid-19 Crisis In early February 2018, a WHO expert committee convened behind closed doors in Geneva “to consider the unthinkable”. “The goal was to identify pathogens with the potential to spread and kill millions but for which there are currently no, or insufficient, countermeasures available.” The Expert Committee had met on two previous occasions, most probably in 2017: “It was the third time the committee, consisting of leading virologists, bacteriologists and infectious disease experts, had met to consider diseases with epidemic or pandemic potential. But when the 2018 list was released two weeks ago [mid February 2018] it included an entry not seen in previous years. In addition to eight frightening but familiar diseases including Ebola, Zika, and Severe Acute Respiratory Syndrome (SARS), the list included a ninth global threat: Disease X.” (Daily Telegraph, emphasis added) It all sounds very scientific based on experts contracted and rewarded by the WHO, under the advice of the Bill and Melinda Gates Foundation: “Disease X represents the knowledge [what knowledge?] that a serious international epidemic could be caused by a pathogen currently unknown to cause human disease”. Experts on the WHO panel say Disease X could emerge from a variety of sources and strike at any time. “History tells us that it is likely the next big outbreak will be something we have not seen before”, said John-Arne Rottingen, chief executive of the Research Council of Norway and a scientific adviser to the WHO committee. “It may seem strange to be adding an ‘X’ but the point is to make sure we prepare and plan flexibly in terms of vaccines and diagnostic tests. “We want to see ‘plug and play’ platforms developed which will work for any, or a wide number of diseases; systems that will allow us to create countermeasures at speed.” (Telegraph) The work of the “expert committee” was followed by two table top simulations respectively in May 2018 and October 2019. The Clade X Simulation: “Parainfluenza Clade X” A few months following the WHO experts’ meeting in Geneva in early 2018, at which a hypothetical Disease X was categorized as a “global threat’, the Clade X table top simulation was conducted Washington D.C. (May 2018) under the auspices of The Johns Hopkins Center for Health Security. “The scenario begins with an outbreak of novel parainfluenza virus that is moderately contagious and moderately lethal and for which there are no effective medical countermeasures”. The virus is called: “Parainfluenza Clade X” “Disease X” and the 201 Global Pandemic Simulation The Hypothetical Disease X Concept developed in 2017-2018 by a WHO Expert Committee of leading virologists and disease experts was simulated in the Event 201 Table Top Simulation of a deadly corona virus pandemic. The Global Pandemic Exercise was held in New York under the auspices of the John Hopkins Bloomberg School of Health, Centre for Heath Security (which hosted the May 2018 Clade X Simulation). The event was sponsored by the Gates Foundation and the World Economic Forum. (Event 201) An October 21, 2019 report “Disease X dummy run: World health experts prepare for a deadly pandemic and its fallout confirms that Disease X was part of the 201 Global Pandemic Simulation: On Friday a panel of 15 high-powered international figures gathered in the ballroom of a New York hotel to “game” a scenario in which a pandemic is raging across the world, killing millions. Health experts fully expect the world to be confronted by a fast-moving global pandemic. The updates were coming into the situation room thick and fast – and the news was not good. The virus was spreading… The former deputy director of the CIA took off her glasses, rubbed her eyes, and addressed the panel. “We also have to consider that terrorists could take advantage of this situation,” she said. “We’re looking at the possibility of famine. There is the potential for outbreaks of secondary diseases.” “I fully expect that we will be confronted by a fast-moving global pandemic,” said Dr Mike Ryan, executive director of the World Health Organisation (WHO) health emergencies programme. Addressing participants – and the 150 observers – before the scenario began, he said that the WHO deals with 200 epidemics every year. It’s only a matter of time before one of those becomes a pandemic – defined as a disease prevalent over a whole country or the world.” (Telegraph, emphasis added) Video: Tedros Stated that Covid was “The First Disease X” Click here to watch the video. Evidence: No Pandemic in Early 2020. Misleading Statements by Dr. Tedros, Fraudulent Decisions In a factual nutshell: WHO Director General Dr. Tedros Adhanom Ghebreyesus launched a Public Health Emergency of International Concern (PHEIC) on January 30th 2020. There was 83 “confirmed cases” outside China for a population of 6.4 billion people. There was no “scientific basis” to justify the launching of a Worldwide Public Health Emergency. On February 20th, 2020: At a briefing in Geneva, the WHO Director General Dr Tedros said that he was “concerned that the chance to contain the coronavirus outbreak was “closing” …“I believe the window of opportunity is still there, but that the window is narrowing.” Those statements were based on 1076 “confirmed cases” outside China. The WHO officially declared a Worldwide pandemic on March 11, 2020 at a time when the number of PCR cases outside China (6.4 billion population) was of the order of 44,279 cumulative confirmed cases. All so-called confirmed cases are the result of the PCR test, which does not detect the virus. In the US on March 9, 2020, there were 3,457 “confirmed cases” out of a population of 329.5 million people. In Canada on March 9, 2020, there were 125 “confirmed cases” out of a population of 38.5 million people. In Germany on March 9, 2020, there were 2948 “confirmed cases” out of a population of 83.2 million people. The above is a summary. Click here and scroll down for references and analysis. The “Disease X” Fear Campaign and the Pandemic Treaty There is vast literature on the Pandemic Treaty and its likely consequences. The Pandemic Treaty consists in creating a global health entity under WHO auspices. It’s the avenue towards “Global Governance” whereby the entire world population of 8 billion would be digitized, integrated into a global digital data bank. All your personal information would be contained in this data bank, leading to the derogation of fundamental human rights as well as the subordination of national governments to dominant financial establishment. The Pandemic Treaty would be tied into the creation of a worldwide digital ID system. According to David Skripac: “A worldwide digital ID system is in the making. [The aim] of the WEF—and of all the central banks [is] to implement a global system in which everyone’s personal data will be incorporated into the Central Bank Digital Currency (CBDC) network.” Peter Koenig describes the underlying process as: “an all-electronic ID – linking everything to everything of each individual (records of health, banking, personal and private, etc.).” Bombshell: A Vaccine for a Hypothetical “Disease X” Pandemic “with an Unknown Pathogen” Announced by Dr. Tedros at Davos24, not to mention Bill Gates’s numerous authoritative statements, governments must prepare for the outbreak of “Disease X”. A State of the Art “Vaccine” allegedly to “Build our Immunity” against “Disease X” (which is a hypothetical construct based on an unknown pathogen) is slated to be developed at Britain’s “Vaccine Development and Evaluation Centre” (UK Health and Security Agency’s (UKHSA) Porton Down campus in Wiltshire, inaugurated in August 2023. “Ministers have opened a new vaccine research centre in the UK where scientists will work on preparing for “disease X”, the next potential pandemic pathogen. Prof Dame Jenny Harries said: “What we’re trying to do now is capture that really excellent work from Covid and make sure we’re using that as we go forward for any new pandemic threats.” She added: “What we try to do here is keep an eye on the ones that we do know. For example, with Covid, we are still here testing all the new variants with the vaccines that have been provided to check they are still effective. “But we are also looking at how quickly we can develop a new test that would be used if a brand new virus popped up somewhere.” … “This state-of-the-art complex will also help us deliver on our commitment to produce new vaccines within 100 days of a new threat being identified.” (The Guardian, emphasis added) The “Disease X” “Vaccine” Is to be Developed at the U.K. Ministry of Defense Science and Technology Porter Down Campus “The Vaccine Development and Evaluation Centre” (VDEC) –which has a mandate to develop “The Disease X” Vaccine– is a civilian research entity under Britain’s National Health Service (NHS) managed by the UK Health and Security Agency (UKHSA) headed by Dame Jennifer Harries (DBE). Of significance VDEC which was inaugurated in August 2023 is located in: The “Defence Science and Technology Laboratory” [Dstl] at Porton Down, Wiltshire, which is one of the U.K.’s Ministry of Defense’s most secretive and controversial military research facilities specializing in the testing of biological and chemical weapons. The UK Health and Security Agency (UKHSA) has initiated a project in global and country-level “Integrated Disease Surveillance” funded by the Bill and Melinda Gates Foundation. A representative of the Gates Foundation is a member of UKHSA’s Advisory Board. What is required is a mass movement to oppose the adoption of the Pandemic Treaty at the World Health Assembly (May 27, 2024). We also call for the immediate cancellation of the Covid-19 “Killer Vaccine.” Ironically to say the least, the WHO Director General Tedros admits that “the momentum had been slowed down by entrenched positions and “a torrent of fake news, lies, and conspiracy theories”. Click here to read Steve Watson’s article titled World Health Organisation Head: Global Compliance Needed For Next Pandemic. https://open.substack.com/pub/michelchossudovsky/p/hypothetical-disease-x-who-pandemic-treaty-fraud It is surely obvious to any dispassionate observer that this coalition of the powerful intends to spring some health crisis upon the people of the world. When have the rich and powerful given a care about the health of poor people? That’ll be never. Pandemics are not a thing. Think back through your life. How many pandemics have there been? Covid wasn’t one. The Spanish flu nonsense wasn’t one. None of the flu like illnesses reported in the 1960s were one. I don’t believe there has ever been even one. Scary infectious diseases are only scary until you stumble across medical research literature going back as far a century and more, in which numerous, serious clinical research studies were set up to detect and measure symptomatic transmission (causing a well person to fall ill with similar symptoms to those of the donor person). Try as they might, that didn’t happen. Contagion in this specific scenario (acute respiratory diseases) does not happen. So when they come at you with the next bunch of lies, try to spot the lies as the mealy mouthed, wet, TV presenters talk nonsense! Then to this “100 day vaccine” idiocy. As you really going to roll your sleeve up and receive an injection of mRNA wrapped in lipid nanoparticles? They will be toxic. Do note that Porton Down, the government’s own formerly named Chemical Defence Establishment, has been tapped as the people to do it! Wouldn’t you want to work with the people who claimed to have whipped up by far the world record speed of vaccine R&D & product delivery? They cut down the time needed by 90%. Surely you’d give the task to those people? So they’re giving it to a military group who haven’t ever done anything like this before? You don’t need a vaccine. Even if everything else was true, it’s out of the question to rustle up a jab in 100 days. Impossible to do it in under several yearrs which, by the way, is FAR FAR longer than the length of time that it’s claimed for the longest lasting pandemic, ever. I hope this helps you to respond appropriately, before the next nonsense arrives! Best wishes Mike 👉 https://t.me/DrMikeYeadon https://donshafi911.blogspot.com/2024/02/hypothetical-disease-x-who-pandemic.html
    OPEN.SUBSTACK.COM
    Hypothetical “Disease X”: The WHO Pandemic Treaty Is a Fraud. Demands Compliance for “Next Pandemic”
    A “vaccine” for a non-existent hypothetical “Disease X” is slated to to be developed at one of UK Ministry of Defense's most secretive and controversial military research facilities specializing in the testing of biological and chemical weapons.
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  • Dissecting “Disease X” And The Pandemic Agreement
    Derrick Broze
    (TLAV) At the World Economic Forum‘s recent annual meeting in Davos, Switzerland, a panel called “Preparing for Disease X” caught the eyes of researchers who are skeptical of the organization and their claimed mission of helping humanity and the planet. The panel included the World Health Organization’s Director-General Tedros Adhanom Ghebreyesus; Shyam Bishen, member of the WEF Executive Committee; and Nisia Trindade Lima, Brazil’s Minister of Health, among others.

    “‘Disease X’ is a placeholder for unknown disease,” Tedros explained to the panel. “You may even call COVID as the first Disease X, and it may happen again.”

    WHO Director-General Tedros referenced the WHO’s Pandemic agreement discussions, stating that countries need to unite against a “common enemy”.

    “This is a common global interest, and very narrow national interest can get in the way,” Tedro stated. “Of course, national interest is natural, but it’s the narrow national interest that can be difficult and is affecting the negotiations even as we speak.”

    The WHO’s 194 member nations are slated to meet in May to adopt some version of the WHO’s pandemic treaty and the International Health Regulations (IHR). Recent drafts of the proposed treaty indicate that it poses a threat to national sovereignty and decision making. Fears of loss of sovereignty have led some nations to push back against the agreement.

    On Monday the United Nations noted that the Pandemic Agreement may not be finalized in May as planned. The news came from a WHO “Informal Session” on the agreement and IHR. During the session Tedros stated that time was “very short” to find consensus. Tedros specifically blamed “conspiracy theories” for the lack of progress on the agreement.

    “The IHR working group are operating amidst a torrent of fake news, lies, and conspiracy theories. There are those who claim the pandemic agreement and IHR will cede sovereignty to WHO and give the WHO Secretary the power to impose lockdowns or vaccine mandates on countries,” Tedros stated. “You know this is fake news, lies, and conspiracy theories. You know these claims are completely false. You know the agreement will give the WHO no such powers. We cannot allow this historic agreement, this milestone in global health, to be sabotaged by those who spread lies.”

    Tedros claimed the agreement “will not and can not” cede the sovereignty of member states over to the WHO. However, the language of the most recent draft makes it clear that member nations are expected to be bound by the provisions within the agreement. As you will see in a moment, documents from the 2017 G20 meeting make it clear the IHR are intended to be followed by member nations of the WHO.

    What is Disease X?

    The phrase “Disease X” has been going viral since the announcement of the WEF panel. The corporate media and the fact checkers have already done their part to assure the masses that it’s only “right wing extremists” who are worried about the talk of this unknown pathogen that could allegedly be “20 times” more deadly than the COVID-19 panic.

    One of the reasons the internet is ablaze with talk of “Disease X” is because the public remembers the Event 201 exercise which took place in October 2019 and simulated a coronavirus pandemic sweeping the world 5 months before the world learned of what they would later call COVID-19. As TLAV has extensively reported, many elements of the Event 201 exercise became reality in 2020. Between 2020 and 2022, many people were banned from social media platforms for asking questions about Event 201.

    Interestingly, Event 201 is also considered to be a test for “Disease X”, and, as noted by WHO Secretary Tedros, COVID-19 could be considered the first Disease X. Now, after the WEF panel discussing the allegedly upcoming “Disease X”, onlookers are wondering if the world should be prepared for another scamdemic.

    So, where did the use of this phrase begin and what does it mean for 2024? This is a brief rundown of some of the various discussions of “Disease X”.

    WEF 2017

    In January 2017, the World Economic Forum announced the creation of the Coalition for Epidemic Preparedness Innovations, or CEPI. The launch of CEPI at the 2017 WEF meeting involved the Wellcome Trust, Bill & Melinda Gates Foundation — both of whom had major roles in the response to COVID-19, providing hundreds of millions of dollars in funding.

    At the WEF 2019 meeting — one year before COVID-19 emerged — there was also discussion of “Disease X” on a panel titled “Disease X: Confronting a New Era of Biological Threats”. The panel was moderated by Jeffrey M. Drazen, Editor-in-Chief of the New England Journal of Medicine, and included panelists Seth F. Berkley, CEO of Gavi, the Vaccine Alliance, and Jeremy Farrar, Director of Wellcome Trust, with closing remarks by Wang Chen, President of the Chinese Academy of Medical Sciences.

    G20 2017: 5C Health Emergency Simulation Exercise

    The G20 held a pandemic simulation exercise known as ‘5C Health Emergency Simulation Exercise’ in Berlin, Germany in May 2017. The name “5C” refers to the five C-topics around which the exercise revolved: communication, collaboration, contributions, coordination and compliance. The simulation involved a fictional novel respiratory virus, the Mountain Associated Respiratory Syndrome (MARS) virus.

    At the same meeting, the G20 released a statement titled “Berlin Declaration of the G20 Health Ministers: Together Today for a Healthy Tomorrow”, which made it clear that the World Health Organization expects member states to comply with the International Health Regulations (IHR).

    In the Berlin Declaration, under the section focused on “compliance” it calls for stronger tools to force compliance from member states. It reads, “However, countries’ compliance with the IHR and with temporary recommendations issued under the IHR needs to be enhanced.” The document also states that “countries not fulfilling their obligations might be perceived by the international community to be violating international law and thus risk reputational damage”.

    As the G20 noted in their declaration, the IHR were passed by the WHO in 2005 and went into effect in 2007. They are considered an “international legal instrument” that is binding on all WHO Member States.

    “We acknowledge that efficient global health crisis management can only be ensured through compliance with the International Health Regulations (IHR). We will act accordingly within our obligations under the IHR and support the leadership and coordination of WHO in the event of health crises of international concern,” the document states.

    It also says the signatories “affirm WHO’s central role as health cluster lead in particular within the United Nations (UN)”. All “stakeholders” are expected to be “involved in preventing, preparing for and responding to current and future health crises, guided by the leadership of WHO”.

    Further, the document states that the “international community needs to fully support the WHO in order for the organization to be able to fulfill its role”.

    It is these sorts of statements which have stoked fears of the WHO interfering with the sovereignty of member states.

    2018: WHO Research Development Blueprint

    In February 2018, the WHO launched the “2018 R&D Blueprint” to focus on diseases which are claimed to represent the highest likelihood of causing a future pandemic. Around this time the WHO added Disease X to the shortlist as a placeholder for a “knowable unknown” pathogen. The WHO said the name “represents the knowledge that a serious international epidemic could be caused by a pathogen currently unknown to cause human disease”. The WHO called for more financing and preparedness for the apparently inevitable future pandemic.

    Dr. Anthony Fauci, former director of the US National Institute of Allergy and Infectious Diseases, told CNN “experience has taught us more often than not the thing that is gonna hit us is something that we did not anticipate”.

    October 2018: The Trudeau Institute War Game

    In addition to Event 201, previous simulations of pandemics have also been touted as preparation for the future event known as “Disease X”. One such simulation took place in October 2018 in Saranac Lake, New York, at a gathering organized by the Trudeau Institute and the State University of New York Upstate Medical University titled, ‘‘Translational Immunology Supporting Biomedical Countermeasure Development for Emerging Vector-Borne Viral Diseases.”

    At this gathering a group of biomedical scientists conducted a “war game” for the fictional Disease X. The attendees included basic scientists, physician-scientists, science support professionals, and organizations and institutions with “experience and expertise in identifying and working to solve major global health problems”.

    Keynote speakers included representatives from the International Vaccine Institute (IVI), Coalition for Epidemic Preparedness Innovations (CEPI), and the U.S. National Institutes of Health (NIH).

    The scientists concluded that the key to preventing a “global health disaster” resulting from Disease X is to pull “existing public health organizations together in a coordinated, vigorous and sustained effort” to deliver a “safe and effective vaccine”. They called for “leveraging pre-developed vaccine platforms such as injectable formulations of DNA, self-replicating RNA, recombinant proteins and viral vectors”.

    March 2020: COVID-19

    After the WHO declared COVID-19 a pandemic we continued to see references to Disease X from numerous scientific journals and health organizations. In March 2020, The Lancet published a study titled “Disease X: accelerating the development of medical countermeasures for the next pandemic“. A couple months later a paper titled “The Next Pandemic: Prepare for ‘Disease X’” was published in the West Journal of Emerging Medicine.

    2021: Disease X Medical Countermeasure Program

    By 2021, John Hopkins University’s Center for Health Security launched the Disease X Medical Countermeasure Program. The program was said to “leverage technologies and vaccine platforms most suitable to the viral families that are likely to cause future catastrophic disease outbreaks”.

    2022: WHO Updates Their “Research & Development Blueprint”

    In November 2022, the WHO announced the launch of a global scientific process to update the list of “priority pathogens” to guide global investment, research, and development (R&D), especially in vaccines, tests, and treatments.

    The WHO convened over 300 scientists to consider the evidence on over 25 virus families and bacteria, including “Disease X.” The scientists made recommendations for which priority pathogens needed further research and investment.

    2023: Disease X Act of 2023

    In June 2023, Congresswoman Lori Trahan of Massachusetts introduced the “Disease X Act of 2023” calling for expanding “the priorities of the Biomedical Advanced Research and Development Authority (BARDA) to specifically include viral threats that have the potential to cause a pandemic”. BARDA was created in 2006 as a response to the claims of anthrax attacks in the United States. The agency has been compared to the controversial Department of Advanced Research and Projects Agency, or DARPA.

    Trahan’s bill calls for establishing a Disease X Medical Countermeasures Program at BARDA by allowing the HHS to award contracts, grants, and cooperative agreements to “promote the development of Disease X medical countermeasures for viral families with pandemic potential”. The bill also calls for directing BARDA to “accelerate and support the advanced research, development, and procurement of countermeasures and products to address Disease X threats”.

    May 2024: The WHO Pandemic Agreement

    With only 3 months until the WHO’s official meeting to vote on the Pandemic Agreement, the clock is ticking for the Predator Class and their biomedical agenda. Will they succeed in forcing the agreement down the throats of skeptical nations? If so, will Disease X magically appear? Will the agreement actually lead to the loss of sovereignty?

    The language in the agreement appears to be clear that nations will be expected to follow the guidelines and recommendations of the WHO during a claimed pandemic. Whether nations will comply and how exactly the WHO could enforce such measures remains to be seen, but the 2017 G20 Berlin Declaration specifically mentions peer pressure from other nations. This could come in the form of public statements or even financial pressure.

    One thing is for certain: those who are paying attention need to know that 2024 is going to be a big year for the Predator Class as they finally attempt to cement their collectivist philosophy in a binding international agreement. Do whatever you can to spread the word and resist their attempts to strip nations and individuals of the right to decide how to respond to claimed health threats.

    https://thefreethoughtproject.com/health/dissecting-disease-x-and-the-pandemic-agreement

    https://donshafi911.blogspot.com/2024/01/dissecting-disease-x-and-pandemic.html
    Dissecting “Disease X” And The Pandemic Agreement Derrick Broze (TLAV) At the World Economic Forum‘s recent annual meeting in Davos, Switzerland, a panel called “Preparing for Disease X” caught the eyes of researchers who are skeptical of the organization and their claimed mission of helping humanity and the planet. The panel included the World Health Organization’s Director-General Tedros Adhanom Ghebreyesus; Shyam Bishen, member of the WEF Executive Committee; and Nisia Trindade Lima, Brazil’s Minister of Health, among others. “‘Disease X’ is a placeholder for unknown disease,” Tedros explained to the panel. “You may even call COVID as the first Disease X, and it may happen again.” WHO Director-General Tedros referenced the WHO’s Pandemic agreement discussions, stating that countries need to unite against a “common enemy”. “This is a common global interest, and very narrow national interest can get in the way,” Tedro stated. “Of course, national interest is natural, but it’s the narrow national interest that can be difficult and is affecting the negotiations even as we speak.” The WHO’s 194 member nations are slated to meet in May to adopt some version of the WHO’s pandemic treaty and the International Health Regulations (IHR). Recent drafts of the proposed treaty indicate that it poses a threat to national sovereignty and decision making. Fears of loss of sovereignty have led some nations to push back against the agreement. On Monday the United Nations noted that the Pandemic Agreement may not be finalized in May as planned. The news came from a WHO “Informal Session” on the agreement and IHR. During the session Tedros stated that time was “very short” to find consensus. Tedros specifically blamed “conspiracy theories” for the lack of progress on the agreement. “The IHR working group are operating amidst a torrent of fake news, lies, and conspiracy theories. There are those who claim the pandemic agreement and IHR will cede sovereignty to WHO and give the WHO Secretary the power to impose lockdowns or vaccine mandates on countries,” Tedros stated. “You know this is fake news, lies, and conspiracy theories. You know these claims are completely false. You know the agreement will give the WHO no such powers. We cannot allow this historic agreement, this milestone in global health, to be sabotaged by those who spread lies.” Tedros claimed the agreement “will not and can not” cede the sovereignty of member states over to the WHO. However, the language of the most recent draft makes it clear that member nations are expected to be bound by the provisions within the agreement. As you will see in a moment, documents from the 2017 G20 meeting make it clear the IHR are intended to be followed by member nations of the WHO. What is Disease X? The phrase “Disease X” has been going viral since the announcement of the WEF panel. The corporate media and the fact checkers have already done their part to assure the masses that it’s only “right wing extremists” who are worried about the talk of this unknown pathogen that could allegedly be “20 times” more deadly than the COVID-19 panic. One of the reasons the internet is ablaze with talk of “Disease X” is because the public remembers the Event 201 exercise which took place in October 2019 and simulated a coronavirus pandemic sweeping the world 5 months before the world learned of what they would later call COVID-19. As TLAV has extensively reported, many elements of the Event 201 exercise became reality in 2020. Between 2020 and 2022, many people were banned from social media platforms for asking questions about Event 201. Interestingly, Event 201 is also considered to be a test for “Disease X”, and, as noted by WHO Secretary Tedros, COVID-19 could be considered the first Disease X. Now, after the WEF panel discussing the allegedly upcoming “Disease X”, onlookers are wondering if the world should be prepared for another scamdemic. So, where did the use of this phrase begin and what does it mean for 2024? This is a brief rundown of some of the various discussions of “Disease X”. WEF 2017 In January 2017, the World Economic Forum announced the creation of the Coalition for Epidemic Preparedness Innovations, or CEPI. The launch of CEPI at the 2017 WEF meeting involved the Wellcome Trust, Bill & Melinda Gates Foundation — both of whom had major roles in the response to COVID-19, providing hundreds of millions of dollars in funding. At the WEF 2019 meeting — one year before COVID-19 emerged — there was also discussion of “Disease X” on a panel titled “Disease X: Confronting a New Era of Biological Threats”. The panel was moderated by Jeffrey M. Drazen, Editor-in-Chief of the New England Journal of Medicine, and included panelists Seth F. Berkley, CEO of Gavi, the Vaccine Alliance, and Jeremy Farrar, Director of Wellcome Trust, with closing remarks by Wang Chen, President of the Chinese Academy of Medical Sciences. G20 2017: 5C Health Emergency Simulation Exercise The G20 held a pandemic simulation exercise known as ‘5C Health Emergency Simulation Exercise’ in Berlin, Germany in May 2017. The name “5C” refers to the five C-topics around which the exercise revolved: communication, collaboration, contributions, coordination and compliance. The simulation involved a fictional novel respiratory virus, the Mountain Associated Respiratory Syndrome (MARS) virus. At the same meeting, the G20 released a statement titled “Berlin Declaration of the G20 Health Ministers: Together Today for a Healthy Tomorrow”, which made it clear that the World Health Organization expects member states to comply with the International Health Regulations (IHR). In the Berlin Declaration, under the section focused on “compliance” it calls for stronger tools to force compliance from member states. It reads, “However, countries’ compliance with the IHR and with temporary recommendations issued under the IHR needs to be enhanced.” The document also states that “countries not fulfilling their obligations might be perceived by the international community to be violating international law and thus risk reputational damage”. As the G20 noted in their declaration, the IHR were passed by the WHO in 2005 and went into effect in 2007. They are considered an “international legal instrument” that is binding on all WHO Member States. “We acknowledge that efficient global health crisis management can only be ensured through compliance with the International Health Regulations (IHR). We will act accordingly within our obligations under the IHR and support the leadership and coordination of WHO in the event of health crises of international concern,” the document states. It also says the signatories “affirm WHO’s central role as health cluster lead in particular within the United Nations (UN)”. All “stakeholders” are expected to be “involved in preventing, preparing for and responding to current and future health crises, guided by the leadership of WHO”. Further, the document states that the “international community needs to fully support the WHO in order for the organization to be able to fulfill its role”. It is these sorts of statements which have stoked fears of the WHO interfering with the sovereignty of member states. 2018: WHO Research Development Blueprint In February 2018, the WHO launched the “2018 R&D Blueprint” to focus on diseases which are claimed to represent the highest likelihood of causing a future pandemic. Around this time the WHO added Disease X to the shortlist as a placeholder for a “knowable unknown” pathogen. The WHO said the name “represents the knowledge that a serious international epidemic could be caused by a pathogen currently unknown to cause human disease”. The WHO called for more financing and preparedness for the apparently inevitable future pandemic. Dr. Anthony Fauci, former director of the US National Institute of Allergy and Infectious Diseases, told CNN “experience has taught us more often than not the thing that is gonna hit us is something that we did not anticipate”. October 2018: The Trudeau Institute War Game In addition to Event 201, previous simulations of pandemics have also been touted as preparation for the future event known as “Disease X”. One such simulation took place in October 2018 in Saranac Lake, New York, at a gathering organized by the Trudeau Institute and the State University of New York Upstate Medical University titled, ‘‘Translational Immunology Supporting Biomedical Countermeasure Development for Emerging Vector-Borne Viral Diseases.” At this gathering a group of biomedical scientists conducted a “war game” for the fictional Disease X. The attendees included basic scientists, physician-scientists, science support professionals, and organizations and institutions with “experience and expertise in identifying and working to solve major global health problems”. Keynote speakers included representatives from the International Vaccine Institute (IVI), Coalition for Epidemic Preparedness Innovations (CEPI), and the U.S. National Institutes of Health (NIH). The scientists concluded that the key to preventing a “global health disaster” resulting from Disease X is to pull “existing public health organizations together in a coordinated, vigorous and sustained effort” to deliver a “safe and effective vaccine”. They called for “leveraging pre-developed vaccine platforms such as injectable formulations of DNA, self-replicating RNA, recombinant proteins and viral vectors”. March 2020: COVID-19 After the WHO declared COVID-19 a pandemic we continued to see references to Disease X from numerous scientific journals and health organizations. In March 2020, The Lancet published a study titled “Disease X: accelerating the development of medical countermeasures for the next pandemic“. A couple months later a paper titled “The Next Pandemic: Prepare for ‘Disease X’” was published in the West Journal of Emerging Medicine. 2021: Disease X Medical Countermeasure Program By 2021, John Hopkins University’s Center for Health Security launched the Disease X Medical Countermeasure Program. The program was said to “leverage technologies and vaccine platforms most suitable to the viral families that are likely to cause future catastrophic disease outbreaks”. 2022: WHO Updates Their “Research & Development Blueprint” In November 2022, the WHO announced the launch of a global scientific process to update the list of “priority pathogens” to guide global investment, research, and development (R&D), especially in vaccines, tests, and treatments. The WHO convened over 300 scientists to consider the evidence on over 25 virus families and bacteria, including “Disease X.” The scientists made recommendations for which priority pathogens needed further research and investment. 2023: Disease X Act of 2023 In June 2023, Congresswoman Lori Trahan of Massachusetts introduced the “Disease X Act of 2023” calling for expanding “the priorities of the Biomedical Advanced Research and Development Authority (BARDA) to specifically include viral threats that have the potential to cause a pandemic”. BARDA was created in 2006 as a response to the claims of anthrax attacks in the United States. The agency has been compared to the controversial Department of Advanced Research and Projects Agency, or DARPA. Trahan’s bill calls for establishing a Disease X Medical Countermeasures Program at BARDA by allowing the HHS to award contracts, grants, and cooperative agreements to “promote the development of Disease X medical countermeasures for viral families with pandemic potential”. The bill also calls for directing BARDA to “accelerate and support the advanced research, development, and procurement of countermeasures and products to address Disease X threats”. May 2024: The WHO Pandemic Agreement With only 3 months until the WHO’s official meeting to vote on the Pandemic Agreement, the clock is ticking for the Predator Class and their biomedical agenda. Will they succeed in forcing the agreement down the throats of skeptical nations? If so, will Disease X magically appear? Will the agreement actually lead to the loss of sovereignty? The language in the agreement appears to be clear that nations will be expected to follow the guidelines and recommendations of the WHO during a claimed pandemic. Whether nations will comply and how exactly the WHO could enforce such measures remains to be seen, but the 2017 G20 Berlin Declaration specifically mentions peer pressure from other nations. This could come in the form of public statements or even financial pressure. One thing is for certain: those who are paying attention need to know that 2024 is going to be a big year for the Predator Class as they finally attempt to cement their collectivist philosophy in a binding international agreement. Do whatever you can to spread the word and resist their attempts to strip nations and individuals of the right to decide how to respond to claimed health threats. https://thefreethoughtproject.com/health/dissecting-disease-x-and-the-pandemic-agreement https://donshafi911.blogspot.com/2024/01/dissecting-disease-x-and-pandemic.html
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  • Hypothetical “Disease X”: The WHO Pandemic Treaty is A Fraud. Demands Compliance for “Next Pandemic”
    “Very narrow national interests should not come in the way”


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    Psychics or psychopaths at the helm?

    —Felicity Arbuthnot, Global Research, January 21, 2024

    Hypothetical “Disease X”

    The WHO Pandemic Treaty is A Fraud

    by

    Michel Chossudovsky

    Introduction

    WHO Director General Tedros Adhanom Ghebreyesus, continues to mislead public opinion Worldwide.

    There is no such thing as “Disease X”. It’s a hypothetical construct by a WHO expert committee (2017-2018) of virologists and disease exports. It was then envisaged in the Clade X Simulation (May 2018) and Event 201 Simulation of a Pandemic (October 2019). Both events were held under the auspices of the John Hopkins Center for Heath Security with the support of the Gates Foundation.“the risks of severe disease from Covid-19 have “dramatically reduced” but another pandemic is all but certain”. says Bill Gates.

    “A potential new pandemic would likely stem from a different pathogen to that of the coronavirus family” (CNBC).

    “We’ll have another pandemic. It will be a different pathogen next time,” Gates said.

    How could he know this in advance?

    WHO Director General’s Presentation at Davos24 WEF

    In his presentation at the Davos24 WEF, the WHO Director General Dr.Tedros recanted Bill Gates’ premonition, pointing to the alleged severity of the Covid-19 crisis initiated in early 2020, in blatant contradiction with official WHO data. (see video below).

    Bill Gates is Tedros’ Mentor. They have a close personal relationship, which occasionally borders on “conflict of interest”.

    Bill Gates, Tedros et al (supported by the WHO committee of experts) are now predicting a new hypothetical pathogen which is allegedly 20 times more deadly than SARS-CoV-2. What absolute nonsense.

    According to Forbes:

    Disease X, a hypothetical unknown threat, is the name used among scientists to encourage the development of countermeasures, including vaccines and tests, to deploy in the case of a future outbreak—the WHO convened a group of over 300 scientists in November 2022 to study the “unknown pathogen that could cause a serious international epidemic,” positing a mortality rate 20 times that of Covid-19″

    300 scientists to study something which is unknown and hypothetical? The media propaganda buzz, quoting “scientific opinion” is “Disease X 20 times more dangerous than Covid”

    A renewed fear campaign 24/7 has been launched, reporting on an alleged new wave of Covid deaths, while totally ignoring the tide of excess mortality resulting from the Covid-19 “vaccine”.

    Video: A Vaccine for a Hypothetical “Disease X” Pandemic.

    “Disease X” Pathogen “Identified” by a WHO Expert Committee Two Years Prior to the Covid-19 Crisis



    In early February 2018 a WHO expert committee convened behind closed doors in Geneva “to consider the unthinkable”.

    click image to access text

    “The goal was to identify pathogens with the potential to spread and kill millions but for which there are currently no, or insufficient, countermeasures available.”

    The Expert Committee had met on two previous occasions, most probably in 2017:

    “It was the third time the committee, consisting of leading virologists, bacteriologists and infectious disease experts, had met to consider diseases with epidemic or pandemic potential.

    But when the 2018 list was released two weeks ago [mid February 2018] it included an entry not seen in previous years.

    In addition to eight frightening but familiar diseases including Ebola, Zika, and Severe Acute Respiratory Syndrome (SARS), the list included a ninth global threat: Disease X.” (Daily Telegraph, emphasis added)

    It all sounds very scientific based on experts contracted by the WHO, under the advice of the Bill and Melinda Gates Foundation:

    “Disease X represents the knowledge [what knowledge?] that a serious international epidemic could be caused by a pathogen currently unknown to cause human disease”.

    Experts on the WHO panel say Disease X could emerge from a variety of sources and strike at any time.

    “History tells us that it is likely the next big outbreak will be something we have not seen before”, said John-Arne Rottingen, chief executive of the Research Council of Norway and a scientific adviser to the WHO committee.

    “It may seem strange to be adding an ‘X’ but the point is to make sure we prepare and plan flexibly in terms of vaccines and diagnostic tests.

    “We want to see ‘plug and play’ platforms developed which will work for any, or a wide number of diseases; systems that will allow us to create countermeasures at speed.” (Telegraph)

    The work of the expert committee was followed by two table top simulations respectively in May 2018 and October 2019.

    The Clade X Simulation: “Parainfluenza Clade X”

    A few months following the WHO experts’ meeting in Geneva in early 2018, at which a hypothetical Disease X was categorized as a “global threat’, the Clade X table top simulation was conducted Washington D.C. (May 2018) under the auspices of The Johns Hopkins Center for Health Security.

    “The scenario begins with an outbreak of novel parainfluenza virus that is moderately contagious and moderately lethal and for which there are no effective medical countermeasures”.

    The virus is called: “Parainfluenza Clade X”

    “Disease X” and the 201 Global Pandemic Simulation



    The Hypothetical Disease X Concept developed in 2017-2018 by a WHO Expert Committee of leading virologists and disease experts was simulated in the Event 201 Table Top Simulation of a deadly corona virus pandemic. The Global Pandemic Exercise was held in New York under the auspices of the John Hopkins Bloomberg School of Health, Centre for Heath Security (which hosted the May 2018 Clade X Simulation). The event was sponsored by the Gates Foundation and the World Economic Forum. (Event 201)

    An October 21, 2019 report “Disease X dummy run: World health experts prepare for a deadly pandemic and its fallout confirms that Disease X was part of the 201 Global Pandemic Simulation:

    On Friday a panel of 15 high-powered international figures gathered in the ballroom of a New York hotel to “game” a scenario in which a pandemic is raging across the world, killing millions.

    Health experts fully expect the world to be confronted by a fast-moving global pandemic. The updates were coming into the situation room thick and fast – and the news was not good. The virus was spreading… The former deputy director of the CIA took off her glasses, rubbed her eyes, and addressed the panel. “We also have to consider that terrorists could take advantage of this situation,” she said. “We’re looking at the possibility of famine. There is the potential for outbreaks of secondary diseases.”

    “I fully expect that we will be confronted by a fast-moving global pandemic,” said Dr Mike Ryan, executive director of the World Health Organisation (WHO) health emergencies programme.

    Addressing participants – and the 150 observers – before the scenario began, he said that the WHO deals with 200 epidemics every year. It’s only a matter of time before one of those becomes a pandemic – defined as a disease prevalent over a whole country or the world.” (emphasis added)



    Video: Tedros stated that Covid was “The First Disease X”

    Evidence: No Pandemic in Early 2020. Misleading Statements by Dr. Tedros, Fraudulent Decisions

    In a Factual Nutshell:

    WHO Director General Dr. Tedros Adhanom Ghebreyesus, launched a Public Health Emergency of International Concern (PHEIC) on January 30th 2020. There was 83 “confirmed Cases” outside China for a population of 6.4 billion people.
    There was no “scientific basis” to justify the launching of a Worldwide Public Health Emergency.
    On February 20th, 2020: At a briefing in Geneva, the WHO Director General Dr Tedros, said that he was “concerned that the chance to contain the coronavirus outbreak was “closing” …“I believe the window of opportunity is still there, but that the window is narrowing.” Those statements were based on 1076 “confirmed cases” outside China.
    The WHO officially declared a Worldwide pandemic on March 11, 2020 at a time when the number of PCR cases outside China (6.4 billion population) was of the order of 44,279 cumulative confirmed cases
    All so-called confirmed cases are the result of the PCR test, which does not detect the virus.
    In the US on March 9, 2020, there were 3,457 “confirmed cases” out of a population of 329.5 million people.
    In Canada on March 9, 2020, there were 125 “confirmed cases” out of a population of 38.5 million people.
    In Germany on March 9, 2020, there were 2948 “confirmed cases” out of a population of 83.2 million people.
    The above is a summary. Scroll down for references and analysis

    The “Disease X” Fear Campaign and the Pandemic Treaty

    There is vast literature on the Pandemic Treaty and its likely consequences.

    The Pandemic Treaty consists in creating a global health entity under WHO auspices. It’s the avenue towards “Global Governance” whereby the entire World population of 8 billion would be digitized, integrated into a global digital data bank.

    All your personal information would be contained in this data bank, leading to the derogation of fundamental human rights as well as the subordination of national governments to dominant financial establishment.

    The Pandemic Treaty would be tied into the creation of a Worldwide digital ID system.

    According to David Scripac

    “A worldwide digital ID system is in the making. [The aim] of the WEF—and of all the central banks [is] to implement a global system in which everyone’s personal data will be incorporated into the Central Bank Digital Currency (CBDC) network.”

    Peter Koenig describes the underlying process as :

    “an all-electronic ID – linking everything to everything of each individual (records of health, banking, personal and private, etc.).”

    Bombshell: A Vaccine for a Hypothetical “Disease X” Pandemic “With an Unknown Pathogen”

    Announced by Dr. Tedros at Davos24, not to mention Bill Gates’ numerous authoritative statements, governments must prepare for the outbreak of “Disease X”.

    A State of the Art “Vaccine” allegedly to “Build our Immunity” against “Disease X” (which is a hypothetical construct based on an unknown pathogen) is slated to be developed at Britain’s “Vaccine Development and Evaluation Centre” (UK Health and Security Agency’s (UKHSA) Porton Down campus in Wiltshire, inaugurated in August 2023.

    “Ministers have opened a new vaccine research centre in the UK where scientists will work on preparing for “disease X”, the next potential pandemic pathogen.

    Prof Dame Jenny Harries said: “What we’re trying to do now is capture that really excellent work from Covid and make sure we’re using that as we go forward for any new pandemic threats.”

    She added: “What we try to do here is keep an eye on the ones that we do know. For example, with Covid, we are still here testing all the new variants with the vaccines that have been provided to check they are still effective.

    “But we are also looking at how quickly we can develop a new test that would be used if a brand new virus popped up somewhere.”

    The opening of the facility is announced after the Covid inquiry heard evidence that previous governments were ill prepared for a pandemic, with its plans focusing too much on the possibility of an influenza pandemic rather than other viruses. The former prime minister David Cameron had admitted this was a “mistake”.

    “This state-of-the-art complex will also help us deliver on our commitment to produce new vaccines within 100 days of a new threat being identified.”

    (The Guardian, emphasis added)

    What we need is a mass movement to oppose the adoption of the Pandemic Treaty at the World Health Assembly (May 27, 2024).

    Ironically to say the least, the WHO Director General Tedros, admits that “the momentum had been slowed down by entrenched positions and “a torrent of fake news, lies, and conspiracy theories”.

    Michel Chossudovsky, Global Research, January 22, 2024, Revised January 24, 2024

    ***

    World Health Organisation Head:

    Global Compliance Needed For Next Pandemic

    by

    Steve Watson

    Original source Modernity

    In an appearance at the globalist World Economic Forum in Davos, the Director General of the World Health Organisation urged that global cooperation will be needed during the next pandemic, and that national interests” hinder compliance.

    In a session titled “Disease X,” Tedros Adhanom Ghebreyesus stated that in order to be “better prepared” and “to understand disease X,” the WHO’s ‘Pandemic Agreement’ needs to be adopted globally.

    “This is about a common enemy,” Tedros continued, adding “without a shared response, we will face the same problem as COVID.”

    He explained that the decline for the legislation is May of this year and member states are negotiating between countries to implement it.

    “This is a common global interest, and very narrow national interests should not come in the way,” he continued, adding “of course national interests are natural, but they could be difficult and affect the negotiations.”

    Tedros also declared that COVID was “the first disease X, and it could happen again.”

    Here is the full exchange:

    Before the cosy chat, Rebel news reporter Avi Yemini confronted Tedros and asked for his opinion on global lockdowns and vaccination mandates.

    He had nothing to say.

    First published by Modernity

    References



    There Never Was a “New Corona Virus”, There Never Was a Pandemic

    By Prof Michel Chossudovsky, January 21, 2024

    Biggest Lie in World History: There Never Was A Pandemic. The Data Base is Flawed. The Covid Mandates including the Vaccine are Invalid,

    By Prof Michel Chossudovsky, May 14, 2023

    The Covid “Killer Vaccine”. People Are Dying All Over the World. It’s A Criminal Undertaking,

    By Prof Michel Chossudovsky, May 24, 2023

    *

    The Worldwide Corona Crisis, Global Coup d’Etat Against Humanity

    Free of Charge for ALL our Readers. Click here to Download

    The Worldwide Corona Crisis, Global Coup d’Etat Against Humanity

    by Michel Chossudovsky

    Michel Chossudovsky reviews in detail how this insidious project “destroys people’s lives”. He provides a comprehensive analysis of everything you need to know about the “pandemic” — from the medical dimensions to the economic and social repercussions, political underpinnings, and mental and psychological impacts.

    “My objective as an author is to inform people worldwide and refute the official narrative which has been used as a justification to destabilize the economic and social fabric of entire countries, followed by the imposition of the “deadly” COVID-19 “vaccine”. This crisis affects humanity in its entirety: almost 8 billion people. We stand in solidarity with our fellow human beings and our children worldwide. Truth is a powerful instrument.”

    Reviews

    This is an in-depth resource of great interest if it is the wider perspective you are motivated to understand a little better, the author is very knowledgeable about geopolitics and this comes out in the way Covid is contextualized. —Dr. Mike Yeadon

    In this war against humanity in which we find ourselves, in this singular, irregular and massive assault against liberty and the goodness of people, Chossudovsky’s book is a rock upon which to sustain our fight. –Dr. Emanuel Garcia

    In fifteen concise science-based chapters, Michel traces the false covid pandemic, explaining how a PCR test, producing up to 97% proven false positives, combined with a relentless 24/7 fear campaign, was able to create a worldwide panic-laden “plandemic”; that this plandemic would never have been possible without the infamous DNA-modifying Polymerase Chain Reaction test – which to this day is being pushed on a majority of innocent people who have no clue. His conclusions are evidenced by renown scientists. —Peter Koenig

    Professor Chossudovsky exposes the truth that “there is no causal relationship between the virus and economic variables.” In other words, it was not COVID-19 but, rather, the deliberate implementation of the illogical, scientifically baseless lockdowns that caused the shutdown of the global economy. –David Skripac

    A reading of Chossudovsky’s book provides a comprehensive lesson in how there is a global coup d’état under way called “The Great Reset” that if not resisted and defeated by freedom loving people everywhere will result in a dystopian future not yet imagined. Pass on this free gift from Professor Chossudovsky before it’s too late. You will not find so much valuable information and analysis in one place. –Edward Curtin

    ISBN: 978-0-9879389-3-0, Year: 2022, PDF Ebook, Pages: 164, 15 Chapters

    Price: $11.50 FREE COPY! Click here (docsend) and download.

    We encourage you to support the eBook project by making a donation through Global Research’s DonorBox “Worldwide Corona Crisis” Campaign Page.

    Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles.

    Related Articles from our Archives

    https://www.globalresearch.ca/world-health-organisation-head-global-compliance-needed-next-pandemic/5847006
    Hypothetical “Disease X”: The WHO Pandemic Treaty is A Fraud. Demands Compliance for “Next Pandemic” “Very narrow national interests should not come in the way” All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name (only available in desktop version). To receive Global Research’s Daily Newsletter (selected articles), click here. Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. New Year Donation Drive: Global Research Is Committed to the “Unspoken Truth” *** Psychics or psychopaths at the helm? —Felicity Arbuthnot, Global Research, January 21, 2024 Hypothetical “Disease X” The WHO Pandemic Treaty is A Fraud by Michel Chossudovsky Introduction WHO Director General Tedros Adhanom Ghebreyesus, continues to mislead public opinion Worldwide. There is no such thing as “Disease X”. It’s a hypothetical construct by a WHO expert committee (2017-2018) of virologists and disease exports. It was then envisaged in the Clade X Simulation (May 2018) and Event 201 Simulation of a Pandemic (October 2019). Both events were held under the auspices of the John Hopkins Center for Heath Security with the support of the Gates Foundation.“the risks of severe disease from Covid-19 have “dramatically reduced” but another pandemic is all but certain”. says Bill Gates. “A potential new pandemic would likely stem from a different pathogen to that of the coronavirus family” (CNBC). “We’ll have another pandemic. It will be a different pathogen next time,” Gates said. How could he know this in advance? WHO Director General’s Presentation at Davos24 WEF In his presentation at the Davos24 WEF, the WHO Director General Dr.Tedros recanted Bill Gates’ premonition, pointing to the alleged severity of the Covid-19 crisis initiated in early 2020, in blatant contradiction with official WHO data. (see video below). Bill Gates is Tedros’ Mentor. They have a close personal relationship, which occasionally borders on “conflict of interest”. Bill Gates, Tedros et al (supported by the WHO committee of experts) are now predicting a new hypothetical pathogen which is allegedly 20 times more deadly than SARS-CoV-2. What absolute nonsense. According to Forbes: Disease X, a hypothetical unknown threat, is the name used among scientists to encourage the development of countermeasures, including vaccines and tests, to deploy in the case of a future outbreak—the WHO convened a group of over 300 scientists in November 2022 to study the “unknown pathogen that could cause a serious international epidemic,” positing a mortality rate 20 times that of Covid-19″ 300 scientists to study something which is unknown and hypothetical? The media propaganda buzz, quoting “scientific opinion” is “Disease X 20 times more dangerous than Covid” A renewed fear campaign 24/7 has been launched, reporting on an alleged new wave of Covid deaths, while totally ignoring the tide of excess mortality resulting from the Covid-19 “vaccine”. Video: A Vaccine for a Hypothetical “Disease X” Pandemic. “Disease X” Pathogen “Identified” by a WHO Expert Committee Two Years Prior to the Covid-19 Crisis In early February 2018 a WHO expert committee convened behind closed doors in Geneva “to consider the unthinkable”. click image to access text “The goal was to identify pathogens with the potential to spread and kill millions but for which there are currently no, or insufficient, countermeasures available.” The Expert Committee had met on two previous occasions, most probably in 2017: “It was the third time the committee, consisting of leading virologists, bacteriologists and infectious disease experts, had met to consider diseases with epidemic or pandemic potential. But when the 2018 list was released two weeks ago [mid February 2018] it included an entry not seen in previous years. In addition to eight frightening but familiar diseases including Ebola, Zika, and Severe Acute Respiratory Syndrome (SARS), the list included a ninth global threat: Disease X.” (Daily Telegraph, emphasis added) It all sounds very scientific based on experts contracted by the WHO, under the advice of the Bill and Melinda Gates Foundation: “Disease X represents the knowledge [what knowledge?] that a serious international epidemic could be caused by a pathogen currently unknown to cause human disease”. Experts on the WHO panel say Disease X could emerge from a variety of sources and strike at any time. “History tells us that it is likely the next big outbreak will be something we have not seen before”, said John-Arne Rottingen, chief executive of the Research Council of Norway and a scientific adviser to the WHO committee. “It may seem strange to be adding an ‘X’ but the point is to make sure we prepare and plan flexibly in terms of vaccines and diagnostic tests. “We want to see ‘plug and play’ platforms developed which will work for any, or a wide number of diseases; systems that will allow us to create countermeasures at speed.” (Telegraph) The work of the expert committee was followed by two table top simulations respectively in May 2018 and October 2019. The Clade X Simulation: “Parainfluenza Clade X” A few months following the WHO experts’ meeting in Geneva in early 2018, at which a hypothetical Disease X was categorized as a “global threat’, the Clade X table top simulation was conducted Washington D.C. (May 2018) under the auspices of The Johns Hopkins Center for Health Security. “The scenario begins with an outbreak of novel parainfluenza virus that is moderately contagious and moderately lethal and for which there are no effective medical countermeasures”. The virus is called: “Parainfluenza Clade X” “Disease X” and the 201 Global Pandemic Simulation The Hypothetical Disease X Concept developed in 2017-2018 by a WHO Expert Committee of leading virologists and disease experts was simulated in the Event 201 Table Top Simulation of a deadly corona virus pandemic. The Global Pandemic Exercise was held in New York under the auspices of the John Hopkins Bloomberg School of Health, Centre for Heath Security (which hosted the May 2018 Clade X Simulation). The event was sponsored by the Gates Foundation and the World Economic Forum. (Event 201) An October 21, 2019 report “Disease X dummy run: World health experts prepare for a deadly pandemic and its fallout confirms that Disease X was part of the 201 Global Pandemic Simulation: On Friday a panel of 15 high-powered international figures gathered in the ballroom of a New York hotel to “game” a scenario in which a pandemic is raging across the world, killing millions. Health experts fully expect the world to be confronted by a fast-moving global pandemic. The updates were coming into the situation room thick and fast – and the news was not good. The virus was spreading… The former deputy director of the CIA took off her glasses, rubbed her eyes, and addressed the panel. “We also have to consider that terrorists could take advantage of this situation,” she said. “We’re looking at the possibility of famine. There is the potential for outbreaks of secondary diseases.” “I fully expect that we will be confronted by a fast-moving global pandemic,” said Dr Mike Ryan, executive director of the World Health Organisation (WHO) health emergencies programme. Addressing participants – and the 150 observers – before the scenario began, he said that the WHO deals with 200 epidemics every year. It’s only a matter of time before one of those becomes a pandemic – defined as a disease prevalent over a whole country or the world.” (emphasis added) Video: Tedros stated that Covid was “The First Disease X” Evidence: No Pandemic in Early 2020. Misleading Statements by Dr. Tedros, Fraudulent Decisions In a Factual Nutshell: WHO Director General Dr. Tedros Adhanom Ghebreyesus, launched a Public Health Emergency of International Concern (PHEIC) on January 30th 2020. There was 83 “confirmed Cases” outside China for a population of 6.4 billion people. There was no “scientific basis” to justify the launching of a Worldwide Public Health Emergency. On February 20th, 2020: At a briefing in Geneva, the WHO Director General Dr Tedros, said that he was “concerned that the chance to contain the coronavirus outbreak was “closing” …“I believe the window of opportunity is still there, but that the window is narrowing.” Those statements were based on 1076 “confirmed cases” outside China. The WHO officially declared a Worldwide pandemic on March 11, 2020 at a time when the number of PCR cases outside China (6.4 billion population) was of the order of 44,279 cumulative confirmed cases All so-called confirmed cases are the result of the PCR test, which does not detect the virus. In the US on March 9, 2020, there were 3,457 “confirmed cases” out of a population of 329.5 million people. In Canada on March 9, 2020, there were 125 “confirmed cases” out of a population of 38.5 million people. In Germany on March 9, 2020, there were 2948 “confirmed cases” out of a population of 83.2 million people. The above is a summary. Scroll down for references and analysis The “Disease X” Fear Campaign and the Pandemic Treaty There is vast literature on the Pandemic Treaty and its likely consequences. The Pandemic Treaty consists in creating a global health entity under WHO auspices. It’s the avenue towards “Global Governance” whereby the entire World population of 8 billion would be digitized, integrated into a global digital data bank. All your personal information would be contained in this data bank, leading to the derogation of fundamental human rights as well as the subordination of national governments to dominant financial establishment. The Pandemic Treaty would be tied into the creation of a Worldwide digital ID system. According to David Scripac “A worldwide digital ID system is in the making. [The aim] of the WEF—and of all the central banks [is] to implement a global system in which everyone’s personal data will be incorporated into the Central Bank Digital Currency (CBDC) network.” Peter Koenig describes the underlying process as : “an all-electronic ID – linking everything to everything of each individual (records of health, banking, personal and private, etc.).” Bombshell: A Vaccine for a Hypothetical “Disease X” Pandemic “With an Unknown Pathogen” Announced by Dr. Tedros at Davos24, not to mention Bill Gates’ numerous authoritative statements, governments must prepare for the outbreak of “Disease X”. A State of the Art “Vaccine” allegedly to “Build our Immunity” against “Disease X” (which is a hypothetical construct based on an unknown pathogen) is slated to be developed at Britain’s “Vaccine Development and Evaluation Centre” (UK Health and Security Agency’s (UKHSA) Porton Down campus in Wiltshire, inaugurated in August 2023. “Ministers have opened a new vaccine research centre in the UK where scientists will work on preparing for “disease X”, the next potential pandemic pathogen. Prof Dame Jenny Harries said: “What we’re trying to do now is capture that really excellent work from Covid and make sure we’re using that as we go forward for any new pandemic threats.” She added: “What we try to do here is keep an eye on the ones that we do know. For example, with Covid, we are still here testing all the new variants with the vaccines that have been provided to check they are still effective. “But we are also looking at how quickly we can develop a new test that would be used if a brand new virus popped up somewhere.” The opening of the facility is announced after the Covid inquiry heard evidence that previous governments were ill prepared for a pandemic, with its plans focusing too much on the possibility of an influenza pandemic rather than other viruses. The former prime minister David Cameron had admitted this was a “mistake”. “This state-of-the-art complex will also help us deliver on our commitment to produce new vaccines within 100 days of a new threat being identified.” (The Guardian, emphasis added) What we need is a mass movement to oppose the adoption of the Pandemic Treaty at the World Health Assembly (May 27, 2024). Ironically to say the least, the WHO Director General Tedros, admits that “the momentum had been slowed down by entrenched positions and “a torrent of fake news, lies, and conspiracy theories”. Michel Chossudovsky, Global Research, January 22, 2024, Revised January 24, 2024 *** World Health Organisation Head: Global Compliance Needed For Next Pandemic by Steve Watson Original source Modernity In an appearance at the globalist World Economic Forum in Davos, the Director General of the World Health Organisation urged that global cooperation will be needed during the next pandemic, and that national interests” hinder compliance. In a session titled “Disease X,” Tedros Adhanom Ghebreyesus stated that in order to be “better prepared” and “to understand disease X,” the WHO’s ‘Pandemic Agreement’ needs to be adopted globally. “This is about a common enemy,” Tedros continued, adding “without a shared response, we will face the same problem as COVID.” He explained that the decline for the legislation is May of this year and member states are negotiating between countries to implement it. “This is a common global interest, and very narrow national interests should not come in the way,” he continued, adding “of course national interests are natural, but they could be difficult and affect the negotiations.” Tedros also declared that COVID was “the first disease X, and it could happen again.” Here is the full exchange: Before the cosy chat, Rebel news reporter Avi Yemini confronted Tedros and asked for his opinion on global lockdowns and vaccination mandates. He had nothing to say. First published by Modernity References There Never Was a “New Corona Virus”, There Never Was a Pandemic By Prof Michel Chossudovsky, January 21, 2024 Biggest Lie in World History: There Never Was A Pandemic. The Data Base is Flawed. The Covid Mandates including the Vaccine are Invalid, By Prof Michel Chossudovsky, May 14, 2023 The Covid “Killer Vaccine”. People Are Dying All Over the World. It’s A Criminal Undertaking, By Prof Michel Chossudovsky, May 24, 2023 * The Worldwide Corona Crisis, Global Coup d’Etat Against Humanity Free of Charge for ALL our Readers. Click here to Download The Worldwide Corona Crisis, Global Coup d’Etat Against Humanity by Michel Chossudovsky Michel Chossudovsky reviews in detail how this insidious project “destroys people’s lives”. He provides a comprehensive analysis of everything you need to know about the “pandemic” — from the medical dimensions to the economic and social repercussions, political underpinnings, and mental and psychological impacts. “My objective as an author is to inform people worldwide and refute the official narrative which has been used as a justification to destabilize the economic and social fabric of entire countries, followed by the imposition of the “deadly” COVID-19 “vaccine”. This crisis affects humanity in its entirety: almost 8 billion people. We stand in solidarity with our fellow human beings and our children worldwide. Truth is a powerful instrument.” Reviews This is an in-depth resource of great interest if it is the wider perspective you are motivated to understand a little better, the author is very knowledgeable about geopolitics and this comes out in the way Covid is contextualized. —Dr. Mike Yeadon In this war against humanity in which we find ourselves, in this singular, irregular and massive assault against liberty and the goodness of people, Chossudovsky’s book is a rock upon which to sustain our fight. –Dr. Emanuel Garcia In fifteen concise science-based chapters, Michel traces the false covid pandemic, explaining how a PCR test, producing up to 97% proven false positives, combined with a relentless 24/7 fear campaign, was able to create a worldwide panic-laden “plandemic”; that this plandemic would never have been possible without the infamous DNA-modifying Polymerase Chain Reaction test – which to this day is being pushed on a majority of innocent people who have no clue. His conclusions are evidenced by renown scientists. —Peter Koenig Professor Chossudovsky exposes the truth that “there is no causal relationship between the virus and economic variables.” In other words, it was not COVID-19 but, rather, the deliberate implementation of the illogical, scientifically baseless lockdowns that caused the shutdown of the global economy. –David Skripac A reading of Chossudovsky’s book provides a comprehensive lesson in how there is a global coup d’état under way called “The Great Reset” that if not resisted and defeated by freedom loving people everywhere will result in a dystopian future not yet imagined. Pass on this free gift from Professor Chossudovsky before it’s too late. You will not find so much valuable information and analysis in one place. –Edward Curtin ISBN: 978-0-9879389-3-0, Year: 2022, PDF Ebook, Pages: 164, 15 Chapters Price: $11.50 FREE COPY! Click here (docsend) and download. We encourage you to support the eBook project by making a donation through Global Research’s DonorBox “Worldwide Corona Crisis” Campaign Page. Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. Related Articles from our Archives https://www.globalresearch.ca/world-health-organisation-head-global-compliance-needed-next-pandemic/5847006
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    Hypothetical "Disease X": The WHO Pandemic Treaty is A Fraud. Demands Compliance for "Next Pandemic"
    There is no such thing as "Disease X". It's a hypothetical construct. According to Bill Gates “Another Pandemic Is All But Certain”… And now, a "Vaccine" is being developed to protect us against a non-existent "Disease X"
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  • Covid mRNA Vaccines Required No Safety Oversight
    Debbie Lerman
    When everyone from the President to your primary care doctor declared loudly and wholeheartedly in December 2020 that the newly FDA-authorized Covid mRNA vaccines were “safe and effective” – what were those claims based on?

    In this article, I will review the contractual and regulatory framework applied by the US government to the initial development, manufacture, and acquisition of the Covid mRNA shots. I will use the BioNTech/Pfizer agreements to illustrate the process.

    The analysis will show that:

    The Covid mRNA vaccines were acquired and authorized through mechanisms designed to rush medical countermeasures to the military during emergencies involving weapons of mass destruction.
    These mechanisms did not require the application of, or adherence to, any laws or regulations related to vaccine development or manufacturing.
    The FDA’s Emergency Use Authorization for the vaccines was based on clinical trials and manufacturing processes conducted with no binding legal standards, no legally proscribed safety oversight or regulation, and no legal redress from the manufacturer for potential harms. (This last point is being challenged in multiple court cases, so far to no avail.)
    What all of this means is that none of the laws or regulations that we count on to protect us from potentially harmful, or deadly, medical products was applied to the Covid mRNA vaccines. The assertion of “safe and effective” was based entirely on aspirations, opinions, beliefs, and presumptions of government employees.

    In Part 1 of this article I will provide a summary of the main contractual and legal points and explain how they excluded any requirements for regulatory oversight. In Part 2, I will go through a detailed analysis of the underlying documentation.

    Contractual Framework for Covid mRNA Vaccines

    When the US government entered into its Covid vaccine agreement with Pfizer, which was acting on behalf of the BioNTech/Pfizer partnership, in July 2020, the agreement encompassed a minimum of 100 million doses of a “vaccine to prevent COVID-19” and a payment of at least $1.95 billion. The agreement also allowed for future procurement of hundreds of millions of additional doses.

    That’s a lot of money for a lot of items, especially since the vaccines had not yet been tested, approved, or manufactured to scale and, as the agreement stated, were purely “aspirational.”

    Obviously, this is not normal procedure. But, then, those were not normal times. The government declared that we were “at war” with a catastrophically dangerous virus that would kill millions and millions of people of all ages unless we could develop “medical countermeasures” (a military term) and get everyone to take them as quickly as possible.

    In keeping with the declaration of war, it was a military framework that was used for acquiring the aspirational products that became known as Covid mRNA vaccines.

    Military Acquisition

    The government side to the agreement with Pfizer was the Department of Defense (DoD), represented by a convoluted chain of parties, each operating as a subcontractor, or co-contractor, for the next.

    You’ll find details about the role of each of these military procurement groups in Part 2 of this article. The important point to recognize is that all of these bodies are charged exclusively with military objectives: “ensuring military readiness,” “enhancing the mission effectiveness of military personnel,” and “supporting the Army and Unified Land Operations, anytime, anywhere.”

    This is crucial, because the laws and procedures governing military procurement have a very different set of assumptions and cost-benefit considerations than those used in civil society.

    In fact, agencies governing civilian and public health, like the NIH, NIAID and HHS, do not have the authority to grant certain types of special acquisition contracts, which is why the Covid vaccine contracts had to be overseen by the Department of Defense.

    Thus, HHS “partnered” with DoD to “leverage DoD’s OTA authorities … which HHS lacked.” [ref]

    What are “OTA authorities?”

    Other Transaction Authority/Agreement (OTA)

    (NOTE: OTA is used interchangeably to refer to Other Transaction Agreement and Other Transaction Authority.)

    The OTA is a procurement method that, according to Department of Defense guidelines, has been used since 1958 to “permit a federal agency to enter into transactions other than contracts, grants, or cooperative agreements.”

    What types of transactions are we talking about?

    First and foremost, the OTA acquisition structure “operates outside the Federal Acquisition Regulations.” This means no federal laws related to government purchases apply to OTAs. Such laws generally involve things like ensuring competition, accounting standards, cost management, record-keeping and labor practices. For purchases of medical products, they also include things like oversight of research on human subjects and privacy laws.

    Why is it a good idea to bypass all these acquisition regulations? For the military, OTAs can provide “access to state-of-the-art technology solutions from traditional and non-traditional defense contractors.” More specifically, according to DARPA (Defense Advanced Research Projects Agency), OTAs are designed to “avoid many of the hurdles that scare away private industry,” including “burdensome regulations.”

    The second defining aspect of OTAs is that they apply to projects that are

    …directly relevant to enhancing the mission effectiveness of personnel of the Department of Defense or improving platforms, systems, components, or materials proposed to be acquired or developed by the Department of Defense, or to improvement of platforms, systems, components, or materials in use by the armed forces.

    In other words, OTA is not a pathway for government acquisitions primarily intended for civilian populations.

    In fact, from the time of OTA inception in 1958 until Covid, the vast majority of OTAs were awarded for weapons, military supplies, and information technologies. For example, in an overview from 2013-2018, the top OTAs dealt with underwater weapons, ground vehicles, rocket propulsion systems, and “technologies related to the use of the electromagnetic spectrum or the information that rides on it.”

    What About OTAs for Medical Products?

    In 2015, DoD announced the establishment of the CBRN Medical Countermeasure Consortium, whose purpose was to use the OTA acquisition pathway to “work with DoD to develop FDA licensed chemical, biological, radiological, and nuclear medical countermeasures.”

    Broadly speaking, this included “prototype technologies for therapeutic medical countermeasures targeting viral, bacterial, and biological toxin targets of interest to the DoD.” Furthermore, such technologies could include “animal models of viral, bacterial or biological toxin disease and pathogenesis, assays, diagnostic technologies, or other platform technologies.”

    Note that there is a mention of FDA licensing, which means a medical product cannot be purchased through OTA without any FDA involvement. The extent of that involvement will be discussed in the section on Regulations below.

    But before we get to the FDA, just looking at what an OTA can be applied to, it does not look like manufacturing 100 million doses of anything is even in the ballpark.

    Pfizer’s Other Transaction Agreement (OTA)

    DoD can make three types of agreements under OTA: research, prototypes, and manufacturing. Importantly, according to National Defense Magazine, the agreements (which are “other than contracts”) are supposed to start with prototypes and then move “from prototypes to production contracts.” In other words, you start with an OTA for a prototype and then get an actual production contract.

    In contrast, the agreement between Pfizer and the US government, routed through the Department of Defense and the CBRN Medical Countermeasure Consortium, classified what Pfizer agreed to deliver as a “prototype project” and “manufacturing demonstration.” As stated in the agreement:

    The intent of this prototype project is to demonstrate that Pfizer has the business and logistics capability to manufacture 100M doses of its currently unapproved mRNA-based COVID-19 vaccine for the Government [(b)(4) redaction]

    So the military acquisition branch of the government is paying Pfizer to show that it can manufacture 100 million doses of a never-before produced or tested product, while also acquiring those 100 million doses, and potentially hundreds of millions more. The “prototype” somehow includes not just the manufacturing process, but also the 100 million doses created through that process.

    Nowhere in the history of Other Transaction Agreements is there anything remotely resembling this conflation of a prototype (“a preliminary model of something,” according to the Oxford English Dictionary) and the manufacturing of millions of exemplars of that prototype. Actually, it is unclear from the wording of the OTA whether the “prototype” applies to the mRNA Covid vaccine, the mRNA platform for manufacturing the vaccine, the actual manufacturing of 100 million vaccines, or all of the above.

    Regulatory Framework for Covid mRNA Vaccines

    What about regulatory oversight of the development and manufacturing processes?

    For pharmaceutical products, like vaccines, this would include: 1) clinical trials to demonstrate the safety and efficacy of the products, and 2) compliance with Good Manufacturing Practices to ensure what is in each dose is actually what is supposed to be in each dose.

    Who is responsible for this type of oversight in the context of Pfizer’s OTA?

    Pfizer will meet the necessary FDA requirements for conducting ongoing and planned clinical trials, and with its collaboration partner, BioNTech, will seek FDA approval or authorization for the vaccine, assuming the clinical data supports such application for approval or authorization.

    What are the FDA requirements “for approval or authorization?”

    According to the Pfizer OTA, those requirements are whatever it takes to “grant an Emergency Use Authorization (“EUA”) under Section 564 of the Federal Food, Drug, and Cosmetic Act.”

    In fact, the two regulations applied to the authorization of the Pfizer mRNA Covid vaccines were EUA and its partner, the PREP Act, which grants legal immunity from prosecution to anyone who has anything to do with the vaccines, unless they commit outright fraud.

    Emergency Use Authorization (EUA)

    EUA is a very special way to authorize a medical countermeasure in very specific types of emergencies. It was designed, according to the Department of Justice, to quickly make available effective vaccines and treatments against – among other CBRN agents – potential biowarfare/bioterror agents like anthrax, botulinum toxin, Ebola, and plague.

    As explained in Harvard Law’s Bill of Health, “Ultimately, it was the War on Terror that would give rise to emergency use authorization.” The article continues,

    The record indicates that Congress was focused on the threat of bioterror specifically, not on preparing for a naturally-occurring pandemic.

    You can read about the details of EUA regulations in part 2 of this article. In summary, an Emergency Use Authorization can be granted by the Food and Drug Administration once the HHS and/or DoD have declared that there is an attack, threat of an attack, or national security threat created by a CBRN agent (a weapon of mass destruction).

    Significantly, as the Harvard Law article explains, EUA was not intended to cover brand-new vaccines:

    The only vaccine ever to have received an EUA prior to the current pandemic was AVA, an anthrax vaccine that had already been formally approved for other purposes.

    This is extremely important: EUA was meant for dire situations of warfare or terrorism, not to protect the entire population from naturally occurring pathogens. For this reason, EUA products do not require the type of legal safety oversight that is applied in civilian contexts by the FDA.

    And without adherence to legal safety standards in clinical trials and manufacturing, there is no way of knowing whether the products, in this case the Covid mRNA vaccines, are actually safe.

    No Legal or Regulatory Standards Apply to the FDA’s Decision to Grant EUA

    Here’s the kicker about EUA: because it was intended to be issued only in war and WMD-related emergencies, there are no legal requirements for how it is issued, beyond the determination of the FDA that such authorization is appropriate. No legal standards for how clinical trials are conducted. No laws regulating the manufacturing processes. Only “reasonable beliefs” based on whatever evidence is available to the FDA at the time that it makes its determination.

    This is how it is described in U.S. Code 360bbb-3, which covers EUA:

    Criteria for issuance of authorization

    An agent referred to in a declaration [by the HHS Secretary] can cause a serious or life-threatening disease or condition
    Based on the totality of scientific evidence available to the Secretary, including data from adequate and well-controlled clinical trials, if available, it is reasonable to believe that
    The product may be effective in diagnosing, treating or preventing such disease or condition
    The known and potential benefits of the product outweigh the known and potential risks, taking into consideration the material threat posed by the CBRN agent(s)
    There is no adequate, approved, and available alternative to the product
    In Its EUA Guidance for Industry and Other Stakeholders, the FDA recommends that EUA applications contain information about clinical trials, manufacturing processes, potential risks, etc. Crucially, as stated at the top of every page, these are merely “nonbinding recommendations.”

    It’s up to the EUA applicant to decide what information to submit, and it’s up to the FDA to decide whether that information meets the “statutory requirements” (as stated above).

    PREP Act

    If you agree to develop, manufacture, and sell hundreds of millions of aspirational products to the government under the contract-like Other Transaction Agreement and bioterror-contingent Emergency Use Authorization, you need very good liability protection.

    This is provided by the PREP (Public Readiness and Emergency Preparedness) Act that was designed to go hand-in-hand with EUA. Again, it is possible to envision a bioterrorism scenario, like an anthrax attack, in which the government needs to get lots of countermeasures very quickly. Many people will inevitably die in the attack, but if there’s a chance that the countermeasure will work, it needs to get made and distributed as quickly as possible. If it has some bad side effects, or even if it kills some people, one could argue that the manufacturer should not be held liable.

    Clearly, this was never intended to apply to a new, untested vaccine used to counter a naturally occurring virus in hundreds of millions of people.

    What, then, are the standards for determining the necessity of a PREP Act declaration?

    Here’s how the Health and Human Services (HHS) website describes the factors considered by the HHS Secretary:

    In deciding whether to issue a PREP Act Declaration, HHS must consider the desirability of encouraging the design, development, clinical testing or investigation, manufacture, labeling, distribution, formulation, packaging, marketing, promotion, sale, purchase, donation, dispensing, prescribing, administering, licensing, and use of the countermeasure recommended in the Declaration. HHS may also consider other relevant factors.

    As with the EUA determination, there are no legally binding standards or directives for issuing a PREP Act. If the products made under EUA cause harm or death, no one involved in making or administering those products can be held accountable, as long as there is accompanying PREP Act protection.

    Conclusion

    The BioNTech/Pfizer Covid mRNA vaccines were authorized for use in the entire population of the United States based on the application of the following sequence of agreements and determinations:

    Department of Defense uses “contract-like” Other Transaction Authority (OTA) to buy aspirational products. DoD is not responsible for overseeing clinical trials or manufacturing. Pfizer is responsible for getting authorization from the FDA.
    The FDA is permitted to issue Emergency Use Authorization (EUA) to Pfizer for mRNA vaccines because the HHS Secretary declares that there is an emergency that warrants EUA.
    FDA makes its EUA determination based on whatever evidence and considerations it feels are appropriate, given the emergency situation. There are no legal standards that apply to the FDA’s considerations, except that it believes the product may be effective, the benefits outweigh the risks based on available information, and there is no alternative product.
    The Health and Human Services Secretary grants total legal immunity through the PREP Act to anyone involved in developing, making, shipping, or administering the vaccines, based on his determination that there is an emergency that justifies this action.
    That’s what the “safe and effective” claim for the BioNTech/Pfizer Covid mRNA vaccines was based on in December 2020, when millions of people – including children and pregnant women – were mandated to take the injections. Objectors were ridiculed, silenced, ostracized, and fired. Harms and deaths were, and continue to be, covered up, uninvestigated, and uncounted.

    Questions About the Legality of the EUA for Covid mRNA Vaccines

    It sounds like something in this whole process must be illegal, right?

    So far, trying to charge pharmaceutical companies with wrongdoing related to Covid vaccines has failed, because the EUA + PREP combo means they were not required to apply any legal/regulatory standards to their clinical studies or manufacturing processes.

    But what about the government?

    Since the OTA, EUA, and PREP regulations are intended for use during a catastrophic CBRN emergency, we might ask ourselves: did the US government believe SARS-CoV-2 was an engineered potential bioweapon? Did the government use what we might consider an extra-legal (in civilian terms) acquisition and authorization process based on the assumption that the entire population was threatened by the equivalent of a bioterrorism or biowarfare attack? It sure seems like they did. And if so, did they have a legal obligation to inform the public of this situation in order to resort to the OTA and EUA procurement and authorization pathway?

    Moreover, even if the government considered Covid-19 to be a disease caused by a potential bioterror agent, how could the HHS Secretary justify an Emergency Use Authorization that required him to determine that “there is a public health emergency that has a significant potential to affect national security” when it was known that Covid-19 was deadly almost exclusively in old and infirm populations?

    In December 2020 the following facts were known about Covid-19 without a reasonable doubt:

    The infection fatality rate (IFR) for the entire population was less than 1%.
    The IFR for anyone under 55 was 0.01% or lower.
    The IFR for children was near zero.
    [ref][ref][ref][ref][ref][ref]

    A disease that has significant potential to affect national security has to be very severe, especially in its effect on the military. Yet in December 2020 military-aged people were known to be at nearly no risk from Covid-19. And still the HHS Secretary determined that there was an emergency that warranted EUA for the mRNA vaccines. And all military personnel were mandated to get the injections.

    I hope that by publishing this information as widely as possible we can eventually find a way to demand some measure of accountability.

    Acknowledgements

    Sasha Latypova and Katherine Watt have been trying to draw attention to this shocking legal and regulatory framework for a long time. I am deeply grateful for, and indebted to, their in-depth research and tireless work to disseminate this information.

    Published under a Creative Commons Attribution 4.0 International License
    For reprints, please set the canonical link back to the original Brownstone Institute Article and Author.

    Author

    Debbie Lerman, 2023 Brownstone Fellow, has a degree in English from Harvard. She is a retired science writer and a practicing artist in Philadelphia, PA.

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    https://brownstone.org/articles/covid-mrna-vaccines-required-no-safety-oversight/
    Covid mRNA Vaccines Required No Safety Oversight Debbie Lerman When everyone from the President to your primary care doctor declared loudly and wholeheartedly in December 2020 that the newly FDA-authorized Covid mRNA vaccines were “safe and effective” – what were those claims based on? In this article, I will review the contractual and regulatory framework applied by the US government to the initial development, manufacture, and acquisition of the Covid mRNA shots. I will use the BioNTech/Pfizer agreements to illustrate the process. The analysis will show that: The Covid mRNA vaccines were acquired and authorized through mechanisms designed to rush medical countermeasures to the military during emergencies involving weapons of mass destruction. These mechanisms did not require the application of, or adherence to, any laws or regulations related to vaccine development or manufacturing. The FDA’s Emergency Use Authorization for the vaccines was based on clinical trials and manufacturing processes conducted with no binding legal standards, no legally proscribed safety oversight or regulation, and no legal redress from the manufacturer for potential harms. (This last point is being challenged in multiple court cases, so far to no avail.) What all of this means is that none of the laws or regulations that we count on to protect us from potentially harmful, or deadly, medical products was applied to the Covid mRNA vaccines. The assertion of “safe and effective” was based entirely on aspirations, opinions, beliefs, and presumptions of government employees. In Part 1 of this article I will provide a summary of the main contractual and legal points and explain how they excluded any requirements for regulatory oversight. In Part 2, I will go through a detailed analysis of the underlying documentation. Contractual Framework for Covid mRNA Vaccines When the US government entered into its Covid vaccine agreement with Pfizer, which was acting on behalf of the BioNTech/Pfizer partnership, in July 2020, the agreement encompassed a minimum of 100 million doses of a “vaccine to prevent COVID-19” and a payment of at least $1.95 billion. The agreement also allowed for future procurement of hundreds of millions of additional doses. That’s a lot of money for a lot of items, especially since the vaccines had not yet been tested, approved, or manufactured to scale and, as the agreement stated, were purely “aspirational.” Obviously, this is not normal procedure. But, then, those were not normal times. The government declared that we were “at war” with a catastrophically dangerous virus that would kill millions and millions of people of all ages unless we could develop “medical countermeasures” (a military term) and get everyone to take them as quickly as possible. In keeping with the declaration of war, it was a military framework that was used for acquiring the aspirational products that became known as Covid mRNA vaccines. Military Acquisition The government side to the agreement with Pfizer was the Department of Defense (DoD), represented by a convoluted chain of parties, each operating as a subcontractor, or co-contractor, for the next. You’ll find details about the role of each of these military procurement groups in Part 2 of this article. The important point to recognize is that all of these bodies are charged exclusively with military objectives: “ensuring military readiness,” “enhancing the mission effectiveness of military personnel,” and “supporting the Army and Unified Land Operations, anytime, anywhere.” This is crucial, because the laws and procedures governing military procurement have a very different set of assumptions and cost-benefit considerations than those used in civil society. In fact, agencies governing civilian and public health, like the NIH, NIAID and HHS, do not have the authority to grant certain types of special acquisition contracts, which is why the Covid vaccine contracts had to be overseen by the Department of Defense. Thus, HHS “partnered” with DoD to “leverage DoD’s OTA authorities … which HHS lacked.” [ref] What are “OTA authorities?” Other Transaction Authority/Agreement (OTA) (NOTE: OTA is used interchangeably to refer to Other Transaction Agreement and Other Transaction Authority.) The OTA is a procurement method that, according to Department of Defense guidelines, has been used since 1958 to “permit a federal agency to enter into transactions other than contracts, grants, or cooperative agreements.” What types of transactions are we talking about? First and foremost, the OTA acquisition structure “operates outside the Federal Acquisition Regulations.” This means no federal laws related to government purchases apply to OTAs. Such laws generally involve things like ensuring competition, accounting standards, cost management, record-keeping and labor practices. For purchases of medical products, they also include things like oversight of research on human subjects and privacy laws. Why is it a good idea to bypass all these acquisition regulations? For the military, OTAs can provide “access to state-of-the-art technology solutions from traditional and non-traditional defense contractors.” More specifically, according to DARPA (Defense Advanced Research Projects Agency), OTAs are designed to “avoid many of the hurdles that scare away private industry,” including “burdensome regulations.” The second defining aspect of OTAs is that they apply to projects that are …directly relevant to enhancing the mission effectiveness of personnel of the Department of Defense or improving platforms, systems, components, or materials proposed to be acquired or developed by the Department of Defense, or to improvement of platforms, systems, components, or materials in use by the armed forces. In other words, OTA is not a pathway for government acquisitions primarily intended for civilian populations. In fact, from the time of OTA inception in 1958 until Covid, the vast majority of OTAs were awarded for weapons, military supplies, and information technologies. For example, in an overview from 2013-2018, the top OTAs dealt with underwater weapons, ground vehicles, rocket propulsion systems, and “technologies related to the use of the electromagnetic spectrum or the information that rides on it.” What About OTAs for Medical Products? In 2015, DoD announced the establishment of the CBRN Medical Countermeasure Consortium, whose purpose was to use the OTA acquisition pathway to “work with DoD to develop FDA licensed chemical, biological, radiological, and nuclear medical countermeasures.” Broadly speaking, this included “prototype technologies for therapeutic medical countermeasures targeting viral, bacterial, and biological toxin targets of interest to the DoD.” Furthermore, such technologies could include “animal models of viral, bacterial or biological toxin disease and pathogenesis, assays, diagnostic technologies, or other platform technologies.” Note that there is a mention of FDA licensing, which means a medical product cannot be purchased through OTA without any FDA involvement. The extent of that involvement will be discussed in the section on Regulations below. But before we get to the FDA, just looking at what an OTA can be applied to, it does not look like manufacturing 100 million doses of anything is even in the ballpark. Pfizer’s Other Transaction Agreement (OTA) DoD can make three types of agreements under OTA: research, prototypes, and manufacturing. Importantly, according to National Defense Magazine, the agreements (which are “other than contracts”) are supposed to start with prototypes and then move “from prototypes to production contracts.” In other words, you start with an OTA for a prototype and then get an actual production contract. In contrast, the agreement between Pfizer and the US government, routed through the Department of Defense and the CBRN Medical Countermeasure Consortium, classified what Pfizer agreed to deliver as a “prototype project” and “manufacturing demonstration.” As stated in the agreement: The intent of this prototype project is to demonstrate that Pfizer has the business and logistics capability to manufacture 100M doses of its currently unapproved mRNA-based COVID-19 vaccine for the Government [(b)(4) redaction] So the military acquisition branch of the government is paying Pfizer to show that it can manufacture 100 million doses of a never-before produced or tested product, while also acquiring those 100 million doses, and potentially hundreds of millions more. The “prototype” somehow includes not just the manufacturing process, but also the 100 million doses created through that process. Nowhere in the history of Other Transaction Agreements is there anything remotely resembling this conflation of a prototype (“a preliminary model of something,” according to the Oxford English Dictionary) and the manufacturing of millions of exemplars of that prototype. Actually, it is unclear from the wording of the OTA whether the “prototype” applies to the mRNA Covid vaccine, the mRNA platform for manufacturing the vaccine, the actual manufacturing of 100 million vaccines, or all of the above. Regulatory Framework for Covid mRNA Vaccines What about regulatory oversight of the development and manufacturing processes? For pharmaceutical products, like vaccines, this would include: 1) clinical trials to demonstrate the safety and efficacy of the products, and 2) compliance with Good Manufacturing Practices to ensure what is in each dose is actually what is supposed to be in each dose. Who is responsible for this type of oversight in the context of Pfizer’s OTA? Pfizer will meet the necessary FDA requirements for conducting ongoing and planned clinical trials, and with its collaboration partner, BioNTech, will seek FDA approval or authorization for the vaccine, assuming the clinical data supports such application for approval or authorization. What are the FDA requirements “for approval or authorization?” According to the Pfizer OTA, those requirements are whatever it takes to “grant an Emergency Use Authorization (“EUA”) under Section 564 of the Federal Food, Drug, and Cosmetic Act.” In fact, the two regulations applied to the authorization of the Pfizer mRNA Covid vaccines were EUA and its partner, the PREP Act, which grants legal immunity from prosecution to anyone who has anything to do with the vaccines, unless they commit outright fraud. Emergency Use Authorization (EUA) EUA is a very special way to authorize a medical countermeasure in very specific types of emergencies. It was designed, according to the Department of Justice, to quickly make available effective vaccines and treatments against – among other CBRN agents – potential biowarfare/bioterror agents like anthrax, botulinum toxin, Ebola, and plague. As explained in Harvard Law’s Bill of Health, “Ultimately, it was the War on Terror that would give rise to emergency use authorization.” The article continues, The record indicates that Congress was focused on the threat of bioterror specifically, not on preparing for a naturally-occurring pandemic. You can read about the details of EUA regulations in part 2 of this article. In summary, an Emergency Use Authorization can be granted by the Food and Drug Administration once the HHS and/or DoD have declared that there is an attack, threat of an attack, or national security threat created by a CBRN agent (a weapon of mass destruction). Significantly, as the Harvard Law article explains, EUA was not intended to cover brand-new vaccines: The only vaccine ever to have received an EUA prior to the current pandemic was AVA, an anthrax vaccine that had already been formally approved for other purposes. This is extremely important: EUA was meant for dire situations of warfare or terrorism, not to protect the entire population from naturally occurring pathogens. For this reason, EUA products do not require the type of legal safety oversight that is applied in civilian contexts by the FDA. And without adherence to legal safety standards in clinical trials and manufacturing, there is no way of knowing whether the products, in this case the Covid mRNA vaccines, are actually safe. No Legal or Regulatory Standards Apply to the FDA’s Decision to Grant EUA Here’s the kicker about EUA: because it was intended to be issued only in war and WMD-related emergencies, there are no legal requirements for how it is issued, beyond the determination of the FDA that such authorization is appropriate. No legal standards for how clinical trials are conducted. No laws regulating the manufacturing processes. Only “reasonable beliefs” based on whatever evidence is available to the FDA at the time that it makes its determination. This is how it is described in U.S. Code 360bbb-3, which covers EUA: Criteria for issuance of authorization An agent referred to in a declaration [by the HHS Secretary] can cause a serious or life-threatening disease or condition Based on the totality of scientific evidence available to the Secretary, including data from adequate and well-controlled clinical trials, if available, it is reasonable to believe that The product may be effective in diagnosing, treating or preventing such disease or condition The known and potential benefits of the product outweigh the known and potential risks, taking into consideration the material threat posed by the CBRN agent(s) There is no adequate, approved, and available alternative to the product In Its EUA Guidance for Industry and Other Stakeholders, the FDA recommends that EUA applications contain information about clinical trials, manufacturing processes, potential risks, etc. Crucially, as stated at the top of every page, these are merely “nonbinding recommendations.” It’s up to the EUA applicant to decide what information to submit, and it’s up to the FDA to decide whether that information meets the “statutory requirements” (as stated above). PREP Act If you agree to develop, manufacture, and sell hundreds of millions of aspirational products to the government under the contract-like Other Transaction Agreement and bioterror-contingent Emergency Use Authorization, you need very good liability protection. This is provided by the PREP (Public Readiness and Emergency Preparedness) Act that was designed to go hand-in-hand with EUA. Again, it is possible to envision a bioterrorism scenario, like an anthrax attack, in which the government needs to get lots of countermeasures very quickly. Many people will inevitably die in the attack, but if there’s a chance that the countermeasure will work, it needs to get made and distributed as quickly as possible. If it has some bad side effects, or even if it kills some people, one could argue that the manufacturer should not be held liable. Clearly, this was never intended to apply to a new, untested vaccine used to counter a naturally occurring virus in hundreds of millions of people. What, then, are the standards for determining the necessity of a PREP Act declaration? Here’s how the Health and Human Services (HHS) website describes the factors considered by the HHS Secretary: In deciding whether to issue a PREP Act Declaration, HHS must consider the desirability of encouraging the design, development, clinical testing or investigation, manufacture, labeling, distribution, formulation, packaging, marketing, promotion, sale, purchase, donation, dispensing, prescribing, administering, licensing, and use of the countermeasure recommended in the Declaration. HHS may also consider other relevant factors. As with the EUA determination, there are no legally binding standards or directives for issuing a PREP Act. If the products made under EUA cause harm or death, no one involved in making or administering those products can be held accountable, as long as there is accompanying PREP Act protection. Conclusion The BioNTech/Pfizer Covid mRNA vaccines were authorized for use in the entire population of the United States based on the application of the following sequence of agreements and determinations: Department of Defense uses “contract-like” Other Transaction Authority (OTA) to buy aspirational products. DoD is not responsible for overseeing clinical trials or manufacturing. Pfizer is responsible for getting authorization from the FDA. The FDA is permitted to issue Emergency Use Authorization (EUA) to Pfizer for mRNA vaccines because the HHS Secretary declares that there is an emergency that warrants EUA. FDA makes its EUA determination based on whatever evidence and considerations it feels are appropriate, given the emergency situation. There are no legal standards that apply to the FDA’s considerations, except that it believes the product may be effective, the benefits outweigh the risks based on available information, and there is no alternative product. The Health and Human Services Secretary grants total legal immunity through the PREP Act to anyone involved in developing, making, shipping, or administering the vaccines, based on his determination that there is an emergency that justifies this action. That’s what the “safe and effective” claim for the BioNTech/Pfizer Covid mRNA vaccines was based on in December 2020, when millions of people – including children and pregnant women – were mandated to take the injections. Objectors were ridiculed, silenced, ostracized, and fired. Harms and deaths were, and continue to be, covered up, uninvestigated, and uncounted. Questions About the Legality of the EUA for Covid mRNA Vaccines It sounds like something in this whole process must be illegal, right? So far, trying to charge pharmaceutical companies with wrongdoing related to Covid vaccines has failed, because the EUA + PREP combo means they were not required to apply any legal/regulatory standards to their clinical studies or manufacturing processes. But what about the government? Since the OTA, EUA, and PREP regulations are intended for use during a catastrophic CBRN emergency, we might ask ourselves: did the US government believe SARS-CoV-2 was an engineered potential bioweapon? Did the government use what we might consider an extra-legal (in civilian terms) acquisition and authorization process based on the assumption that the entire population was threatened by the equivalent of a bioterrorism or biowarfare attack? It sure seems like they did. And if so, did they have a legal obligation to inform the public of this situation in order to resort to the OTA and EUA procurement and authorization pathway? Moreover, even if the government considered Covid-19 to be a disease caused by a potential bioterror agent, how could the HHS Secretary justify an Emergency Use Authorization that required him to determine that “there is a public health emergency that has a significant potential to affect national security” when it was known that Covid-19 was deadly almost exclusively in old and infirm populations? In December 2020 the following facts were known about Covid-19 without a reasonable doubt: The infection fatality rate (IFR) for the entire population was less than 1%. The IFR for anyone under 55 was 0.01% or lower. The IFR for children was near zero. [ref][ref][ref][ref][ref][ref] A disease that has significant potential to affect national security has to be very severe, especially in its effect on the military. Yet in December 2020 military-aged people were known to be at nearly no risk from Covid-19. And still the HHS Secretary determined that there was an emergency that warranted EUA for the mRNA vaccines. And all military personnel were mandated to get the injections. I hope that by publishing this information as widely as possible we can eventually find a way to demand some measure of accountability. Acknowledgements Sasha Latypova and Katherine Watt have been trying to draw attention to this shocking legal and regulatory framework for a long time. I am deeply grateful for, and indebted to, their in-depth research and tireless work to disseminate this information. Published under a Creative Commons Attribution 4.0 International License For reprints, please set the canonical link back to the original Brownstone Institute Article and Author. Author Debbie Lerman, 2023 Brownstone Fellow, has a degree in English from Harvard. She is a retired science writer and a practicing artist in Philadelphia, PA. View all posts Your financial backing of Brownstone Institute goes to support writers, lawyers, scientists, economists, and other people of courage who have been professionally purged and displaced during the upheaval of our times. You can help get the truth out through their ongoing work. https://brownstone.org/articles/covid-mrna-vaccines-required-no-safety-oversight/
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    Covid mRNA Vaccines Required No Safety Oversight ⋆ Brownstone Institute
    The FDA’s Emergency Use Authorization for the vaccines was based on clinical trials and manufacturing processes conducted with no binding legal standards, no legally proscribed safety oversight or regulation, and no legal redress from the manufacturer for potential harms. (This last point is being challenged in multiple court cases, so far to no avail.)
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