In this article you state that July 15 was the day before the event in Butler, PA. The event was on July 13. July 15 was the Monday after the event. July 12 was the date of the Put in question. Just FYI.
Well, Trump did Covid, that one was down to him with his Operation Warp Speed, 9/11 was about the Arabs wanting to go to Jihad against America, what do they call you - The Great Evil? - and Trump's recent assassination attempt seems to have had Black rock and Microsoft involved, the computer "outage" just at the right time to benefit greatly from that having happened.
If Trump is relected, let's hope he remembers Black Rock and Bill Gates when he uses his new Presidential powers to catch and "get" his enemies, shall we?:
From Kyle Young: On March 21, 2021 I posted this piece about the press conference Donald Trump held on October 6, 2017 (above). Some of you may recall this strange event. Trump was standing with many of the military brass and taking questions from reporters. He cryptically said this meeting was “the calm before the storm”. As he was leaving a reporter pressed him about ‘what storm’ and he ominously said, “You’ll find out”. As you will learn, we got part of the picture two months later and even more later.
As that press conference was unfolding a select few were working on this Act. Here is the first paragraph of this legislation.
To amend the Federal Food, Drug, and Cosmetic Act to authorize additional emergency uses for medical products to reduce deaths and severity of injuries caused by agents of war, and for other purposes. <<NOTE: Dec. 12, 2017 - [H.R. 4374]>>
According to the US Army Medical Research and Development Command this legislation -
Expands FDA's emergency use authorization (EUA) authority under §564 of the FD&C Act to allow FDA to issue EUAs for emergency use of unapproved medical products or unapproved uses of approved medical products to address additional types of threats (beyond CBRN agents) related to attack with an "agent or agents that may cause, or are otherwise associated with, an imminently life-threatening and specific risk to the United States military forces" (see §1(a), P.L. 115-92);
Allows the Secretary of Defense to request, and authorizes FDA to take, specific actions to expedite the development of medical products, and the review of investigational submissions, applications for approval/licensure, and submissions/notifications for clearance for such medical products reasonably likely to diagnose, prevent, treat, or mitigate a specific and life-threatening risk to the U.S. military (see §1(b), P.L. 115-92).
Among other things, this legislation grants enormous powers of cooperation between the Department of Defense (DoD) and the FDA. It essentially allows the Secretary of Defense to tell the FDA to authorize drug companies to use the American public as guinea pigs under the auspices of an EUA (Emergency Use Authorization, which allows experimental jabs to be given to the masses). This is unprecedented. Why is the Secretary of Defense telling the FDA what to do? Could it have anything to do with the idea that the jabs are bioweapons meant to cull the population?
As CNN reported here, this legislation was signed into law by President Trump on December 12, 2017, a little over two months after Trump’s cryptic press conference with the military brass.
On April 10, 2021 I posted this piece which delved even deeper into the role Trump played initiating the plandemic. It focuses on Trumps declaration of a covid emergency.
Why is declaring covid an emergency so important to the plan? Without a “declared emergency” none of the ensuing steps could be taken; the EUA, Trumps Operation Warp Speed, the lockdowns, mandates, closures nor the billions of taxpayer dollars authorized by the Trump administration to develop and distribute the jabs.
As I pointed out in earlier posts here, here and here, the infrastructure to make all of this possible has been under development for decades. Slowly but surely, the government, working hand in hand with the DoD and Big Pharma, have programmed us to think that viruses constitute a medical emergency (a premise I’ve contested for a long time, most recently here) and that the US Constitution can be suspended to deal with such an emergency. It cannot. To make all of this seemingly possible they’ve created this completely illegal infrastructure to generate the illusion that they have the legal authority to impose mandates, lockdowns and… jabs. Trump used all of that smoke and all of those mirrors to the max.
emergency use authorization (eua) the key to the dark kingdom
One of the most insidious pieces of legislation in this unconstitutional scheme was the Prep Act. Here’s the first sentence from Wikipedia describing the Prep Act.
The Public Readiness and Emergency Preparedness Act (PREPA), passed by the United States Congress and signed into law by President of the United States George W. Bush in December 2005 (as part of Pub.L. 109–148 (text) (PDF)), is a controversial tort liability shield intended to protect vaccine manufacturers from financial risk in the event of a declared public health emergency.
Christine,
In this article you state that July 15 was the day before the event in Butler, PA. The event was on July 13. July 15 was the Monday after the event. July 12 was the date of the Put in question. Just FYI.
This confirms all I wrote about Trump being attacked by the Shadow Men who also did COVID and 9/11.
Well, Trump did Covid, that one was down to him with his Operation Warp Speed, 9/11 was about the Arabs wanting to go to Jihad against America, what do they call you - The Great Evil? - and Trump's recent assassination attempt seems to have had Black rock and Microsoft involved, the computer "outage" just at the right time to benefit greatly from that having happened.
If Trump is relected, let's hope he remembers Black Rock and Bill Gates when he uses his new Presidential powers to catch and "get" his enemies, shall we?:
From Kyle Young: On March 21, 2021 I posted this piece about the press conference Donald Trump held on October 6, 2017 (above). Some of you may recall this strange event. Trump was standing with many of the military brass and taking questions from reporters. He cryptically said this meeting was “the calm before the storm”. As he was leaving a reporter pressed him about ‘what storm’ and he ominously said, “You’ll find out”. As you will learn, we got part of the picture two months later and even more later.
As that press conference was unfolding a select few were working on this Act. Here is the first paragraph of this legislation.
To amend the Federal Food, Drug, and Cosmetic Act to authorize additional emergency uses for medical products to reduce deaths and severity of injuries caused by agents of war, and for other purposes. <<NOTE: Dec. 12, 2017 - [H.R. 4374]>>
As you can see, this legislation was included in HR 4374 https://www.congress.gov/bill/117th-congress/house-bill/4374.
According to the US Army Medical Research and Development Command this legislation -
Expands FDA's emergency use authorization (EUA) authority under §564 of the FD&C Act to allow FDA to issue EUAs for emergency use of unapproved medical products or unapproved uses of approved medical products to address additional types of threats (beyond CBRN agents) related to attack with an "agent or agents that may cause, or are otherwise associated with, an imminently life-threatening and specific risk to the United States military forces" (see §1(a), P.L. 115-92);
Allows the Secretary of Defense to request, and authorizes FDA to take, specific actions to expedite the development of medical products, and the review of investigational submissions, applications for approval/licensure, and submissions/notifications for clearance for such medical products reasonably likely to diagnose, prevent, treat, or mitigate a specific and life-threatening risk to the U.S. military (see §1(b), P.L. 115-92).
Among other things, this legislation grants enormous powers of cooperation between the Department of Defense (DoD) and the FDA. It essentially allows the Secretary of Defense to tell the FDA to authorize drug companies to use the American public as guinea pigs under the auspices of an EUA (Emergency Use Authorization, which allows experimental jabs to be given to the masses). This is unprecedented. Why is the Secretary of Defense telling the FDA what to do? Could it have anything to do with the idea that the jabs are bioweapons meant to cull the population?
As CNN reported here, this legislation was signed into law by President Trump on December 12, 2017, a little over two months after Trump’s cryptic press conference with the military brass.
On April 10, 2021 I posted this piece which delved even deeper into the role Trump played initiating the plandemic. It focuses on Trumps declaration of a covid emergency.
Why is declaring covid an emergency so important to the plan? Without a “declared emergency” none of the ensuing steps could be taken; the EUA, Trumps Operation Warp Speed, the lockdowns, mandates, closures nor the billions of taxpayer dollars authorized by the Trump administration to develop and distribute the jabs.
As I pointed out in earlier posts here, here and here, the infrastructure to make all of this possible has been under development for decades. Slowly but surely, the government, working hand in hand with the DoD and Big Pharma, have programmed us to think that viruses constitute a medical emergency (a premise I’ve contested for a long time, most recently here) and that the US Constitution can be suspended to deal with such an emergency. It cannot. To make all of this seemingly possible they’ve created this completely illegal infrastructure to generate the illusion that they have the legal authority to impose mandates, lockdowns and… jabs. Trump used all of that smoke and all of those mirrors to the max.
emergency use authorization (eua) the key to the dark kingdom
One of the most insidious pieces of legislation in this unconstitutional scheme was the Prep Act. Here’s the first sentence from Wikipedia describing the Prep Act.
The Public Readiness and Emergency Preparedness Act (PREPA), passed by the United States Congress and signed into law by President of the United States George W. Bush in December 2005 (as part of Pub.L. 109–148 (text) (PDF)), is a controversial tort liability shield intended to protect vaccine manufacturers from financial risk in the event of a declared public health emergency.