patrick.net

Overall characterization of what is going on: the federal and most of the state governments are gone and captured. Whatever is running the federal gov agencies (e.g. HHS) really intends to kill you, or at least substantially injure you, damage your reproductive capacity and repossess your assets in the process. The aim is to reduce the population and terrorize the survivors enough to establish a totalitarian control over much of the world’s territory. Nobody is coming to save you, your survival and that of your children is in your hands only. Do not comply.

We are at war in the US and globally. Public Health Emergencies have largely the same legal status as war declarations (National Emergency). PHE (PHEIC) declarations effectively suspend the Constitution, let the Executive branch (including DOD and HHS) usurp the power and neuter the Legislative and Judicial branches of the government. Once initiated, there are no stopping conditions.

PREP Act declarations by the HHS Secretary can be viewed as announcements of use of certain types of weapons as well as provision of liability coverage for those deploying them (largely through the healthcare system), just as military in combat zones are exempt from injury claims from those they kill and injure as enemy combatants.

Deployment of the bio-chemical poisons advertised as “vaccines” or any other medical countermeasures (for covid or another made-up “pandemic”) does not depend on federal or state pharmaceutical regulations and are not subject to any consumer or research subject protections, such as informed consent rules. Thus, any activities advertised as “clinical trials” or regulatory actions in relation to these bio-chemical materials are theatrics to fool the public and especially the professional class into believing this is a health event, and that they are receiving (or administering) treatments. This is explained in more detail in this post - Intent to Harm.

Bio-chemical poisons advertised as “vaccines” were pushed on unsuspecting public and fooled professionals under a “bait and switch” scheme where FDA approval (BLA) was a sham and the actual delivered product always (with exception of tiny amount of 35K doses) substituted with the Emergency Use Authorized (EUA) version of the product. This is explained in detail in this post, as well as the allegations in this important legal complaint.

The role of DOD: All covid countermeasures were ordered by the US Department of Defense (DOD), typically as “demonstrations” and “prototypes” via Other Transactions Authority contracts. DOD partnered with HHS in order to over-ride the OTA restrictions of both, the DOD and HHS. DOD oversaw the development, manufacture, and distribution of the countermeasures. Hundreds of contracts for covid countermeasures became available via FOIA and SEC disclosures in partially-redacted form. The contracts include the removal of all liability for the manufacturers and any contractors along the supply and distribution chain under the 2005 PREP Act and related federal legislation except in case of willful misconduct. While the DOD/BARDA countermeasure contracts refer to safety and efficacy requirements for vaccines and mention current Good Manufacturing Practices (cGMP) compliance, this language in contract is designed to fool the reader as it is in fact unenforceable. To date (2024) no legal case filed against vaccine makers citing contractual obligation to deliver safe and effective vaccine has succeeded. These compliance items are explicitly carved out as “not in scope” of the contract and not being paid for nor ordered by the US Government. Judge Truncale agreed with this interpretation when dismissing Brook Jackson’s case v Pfizer under False Claims Act. The case is now being appealed.

Use of Emergency Use Authorized (EUA) covered countermeasures under a declared Public Health Emergency cannot constitute a clinical investigation (21 USC 360bbb-3(k)), therefore these countermeasures could not be tested for safety or efficacy in accordance with US law (21 CFR 312 and 21 CFR 601), nor could compliance with current Good Manufacturing Practices (cGMP) or Good Distribution Practices (GxP in general) be enforced by the FDA. This legal fact was known to high-level FDA officials, to DOD and BARDA officials and to the pharmaceutical companies signing these contracts. This fact was not known to the public, clinical investigators, clinical trial subjects, or the lower-level employees of the pharmaceutical companies and the US Government.

EUA Countermeasures under Public Health Emergency are neither investigational nor experimental! The federal government found a way to break the FD&C Act by creating a separate section in it (random number 564) and making up a new “regulatory” pathway that resides entirely outside of all pharmaceutical regulations: NO investigational review board, NO informed consent and NO cGMP compliance apply to things called “EUA countermeasures under Public Health Emergency”. No matter how adulterated or misbranded (filled with poison and wrapped in a false label) - US Code states that this is totally fine and allowed because HHS Secretary says so. The EUA law is explained in detail in this memo, which you can use to communicate with health care providers and others who are pushing these poisons on you and your children.

The implications of the above can not be overstated. Senior Executive Service officials within the U.S. Government authorized and funded the deployment of bio-chemical poisons on Americans and others without clarifying their “prototype” and “large scale demonstration” legal status, making the materials not subject to normal regulatory oversight, all while knowingly and willfully maintaining a fraudulent pseudo-“regulatory” presentation to the public.

These poisons have harmed and killed and continue to harm and kill Americans and other people around the world.

The Covid countermeasures deployment program has been partially coordinated through the quasi-government Public Health Emergency Medical Countermeasures Enterprise (PHEMCE) and via several other public, private, hybrid and quasi-governmental entities, including but not limited to: the FDA’s Medical Countermeasures Initiative (MCMi); BARDA; and the Medical Chemical, Biological, Radiological, Nuclear [CBRN] Defense Consortium (MCDC).[1]

Pandemic Preparedness is a federal quasi-government racketeering enterprise (here, here and here), and a mass murder/mass injury campaign orchestrated by the CIA/DOD/HHS and several other federal agencies. The purpose is to establish a global government regime of control and enslavement that will allow to replace already fake currencies with even more fake digital tokens CBDCs. This objective goes hand-in-hand with other globalist objectives. These objectives include reduction of the population in the name of “saving the planet”, asset transfer to cronies away from independent private sector (whatever is left of it), looting of public money, creation of government-dependent and therefore highly compliant slave class (dependent on extremely expensive “health” care, dependent on welfare, mentally ill, having to care for vaccine-disabled children, brainwashed into depraved self-destructive ideologies, including but not limited to DEI, addicted to propaganda and fear, addicted to drugs, etc.)

Private pharma corporations are used by the PHEMCE cartel as front to launder the poison made by the CIA/DOD controlled bio-manufacturing assets such as Resilience, Moderna, Emergent Biosolutions, and many other “biodefense” contractors. Pharmas are co-conspirators in the mass murder, however they are corporate shells used to both fool the public with brand names, illusion of regulated, compliant manufacturing (not at all in reality, see above), and launder massive profits resulting from no-risk “investment” of $billions of public money. Prosecution of pharmas for fraud under the EUA Countermeasures laws and PREP Act is mostly a fool’s errand, designed to fail.

Pandemics do not exist naturally. It is not possible for a natural infectious disease to spread all over the world simultaneously. Any local communicable diseases self extinguish. The vast majority to what is presented to the public as historical pandemics are diseases related to lack of water sanitation from human and animal waste, crowding and infestation with rats, fleas, etc. These include diseases that are attributable to bacteria - e.g. cholera and the plague. Spanish Flu was severely misrepresented as a “pandemic”, decades after the fact. It wasn’t considered one by the International Sanitary Convention (predecessor to WHO, 1850 - 1949), also here.

Pandemics do not exist, they are faked by the governments with prohibited bio-chemical agents manufactured utilizing “infectious disease research” loophole of the International Bioweapons Convention, and massive amounts of engineered virus fear porn, fake PCR and hospital murder protocols. US Government has a long, well-documented history of deploying chemical, biological and psychological weapons on unsuspecting targets, and on human subjects without proper consent. “Pandemic preparedness” is a murderous government scam, from which a huge parasitic, militaristic industry is deriving profits and power. This Cartel is managed by DARPA/DTRA and DOD-affiliated “defense” consortia which include all federal agencies acting as “One Government” and biopharmaceutical companies, academia, healthcare providers and many other entities. ...

Six primary enabling statutes include:

Title 21 – Federal Food and Drugs Act, at §360bbb et seq, “Expanded access to unapproved therapies and diagnostics,” as established in 1997;

Title 42 – Public Health Service Act, at §247d et seq, “Public health emergencies,” as established in 1983;

Title 42 – Public Health Service Act, at §300hh et seq, “National All-Hazards Preparedness for Public Health Emergencies,” as established in 2002;

Title 42 – Public Health Service Act, at §300aa-1 et seq, “Vaccines,” as established in 1986;

Title 10 – Armed Forces Act, at §4021 et seq, “Research projects: transactions other than contracts and grants,” as established for DoD use for “prototype” contracting in 2015;

Title 50, Chapter 32, §1511 et seq, “Chemical and Biological Warfare,” as established in 1969.

UK lawmaker stuns parliament with call for members of ‘Covid cabal’ to face death penalty

by WorldTribune Staff, March 17, 2024

British Member of Parliament Andrew Bridgen last week called for the death penalty for Bill Gates and the “Covid cabal” which he said committed “crimes against humanity” during the Covid pandemic.

“Heads of governments around the world and others below them have engaged in what is tantamount to treason against the public,” declared Bridgen in response to a rebuttal from his colleague Penny Mordaunt, who is a long-term World Economic Forum (WEF) member.

During a round of Business Questions in the UK House of Commons, Bridgen said: “I’ve always opposed capital punishment on the principle that it’s wrong to take a life so it can’t be right for the state to take a life in revenge. Events have caused me to reconsider my position.”

Bridgen continued: “So can we have a debate on crimes against humanity and the appropriate punishment for those who perpetuate, collude and cover up for these atrocities, atrocities and crimes so severe that the ultimate punishment may be required?”

This, he further explained, had long been understood about respiratory viruses such as those that cause the common cold and influenza, and this same quality was quickly ascertained about SARS-CoV-2.

Flu "shot" ineffective.

WE MUST INVESTIGATE THE COVID CATASTROPHE

A plea by Ex-Captain Graham Hood - Parliament House, Canberra

Ex-Captain Graham Hood has testified before Senator Malcolm Roberts at Parliament House, Canberra on 21 March 2024 regarding the damage done by the government’s COVID policies.

After all the unnecessary deaths, Covid “vaccine” injuries, hundreds of billions of dollars wasted, the collapse of human rights and abuse of government power…….why can’t we have a Royal Commission? The cover up must end. We must know the truth. The Prime Minister previously supported a Royal Commission before the Federal election but now he is resisting. We now know his word is not his bond.

I was appalled recently at the First Covid Debate on 14th March at NSW Parliament House Sydney when I heard a comment from an individual in the audience disparage the character of Graham Hood and his media partner Johnny Larter (Club Grubberry). Maybe that individual should spend 19 minutes and listen to somebody who really cares about Australians and Australia - listen to a true patriot who has given so much. These days, few who are in a position to really make a difference, like Senator Malcolm Roberts, are prepared to stand and be counted. It is heartbreaking.

Trump just needs to go.

I remember at various jobs that my employers used to heavily push the flu shot. Schwab did for sure.

He's hardly a perfect choice, not even a good choice, but do you have any alternative?

I think RFK Jr is a slightly better alternative, because of his stance on the vaxx.

doctors who tried to prescribe it could lose licenses. pharmacists who filled it could lose licenses. and enforcement was rabid. suddenly, a safe, generic wonderdrug was verboten.

now, call me mr cynical paws, but one cannot help but wonder if the reason for this was less than pure.

here’s the text for EMA (emergency use authorization) drugs like the covid vaccines, paxlovid, and remdesivir.

notice anything? ...

yup. you cannot have an EMA if there is an adequate, approved alternative available. that’s quite an incentive set to gang tackle anything evincing efficacy off the shelves if you’re about to bring the most profitable pharma products in history to market at “warp speed” and your (up until very recently) commissioner scotty “show me the money” gottlieb just jumped ship for the pfizer board right in the middle of his term. ...

no one is really paying any meaningful price. no one got in trouble, got accused of crimes, malpractice, or iatrocide.

and that just means there all still waiting in the wings to do it again and the grift goes on. same prison. no redemption.

if you want change, there need to be consequences.

if you want change, we need to name names and call people out. this was not an accident, it was a plan, a playbook.

i'd really love to find out: who concocted and crafted this message?

who green lit putting it out?

seems like something the public should know and probably someone who really ought not be working at FDA anymore.

But … is covid over? You might say it’s not over till we get justice for everyone harmed by the defective jab products and the nefarious hospital schemes. Never leave a man behind.

n a significant blow to patient autonomy, informed consent has been quietly revoked just 77 years after it was codified in the Nuremberg Code.

On the 21st of December 2023, as we were frantically preparing for the festive season, the Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) issued a final ruling to amend a provision of the 21st Century Cures Act. This allowed

…an exception from the requirement to obtain informed consent when a clinical investigation poses no more than a minimal risk to the human subject…

This ruling went into effect on January 22nd, 2024, which means it’s already standard practice across America.

I had the honor of interviewing the Belgian virologist Geert Vanden Bossche on Friday for my podcast, and he had quite a sobering message. “What I am predicting,” he said, “is a massive, massive tsunami” of illness and death among highly-vaccinated populations with dysregulated immune systems.

“You commit errors or even crimes at the very small scale, you can hide them,” he said (at around 47:00 minutes into the hour-long discussion). “I have seen this happen with the Ebola vaccination with Africa a number of years ago. . . . However, if you do this at the very large scale, like what has happened with this mass [Covid] vaccination campaign, the truth will surface. And those who have committed these crimes who have been lying to the people, who have not been taking care of the health and safety of the people, will be severely, severely punished. . . . If these people would now go out and say, ‘Yeah, wait a minute, we have been making some mistakes, it wasn’t all right, we have to correct them, we have to revise our opinion,' these people will be stoned in the streets. . . . They can only hope that something will happen that will distract from this issue, but it won’t. . . . The truth will surface: this has been a large-scale experiment of gain-of-function on the very human population. This will be something that will be reported in history for many many generations to come.” ...

Now that you’ve had an ice-cold shower, consider some further implications of this scenario. One is that the government and its public health officials may try to attribute the blame for this to the “Disease X” story they’ve been peddling for about a year, the “next pandemic,” something entirely new. That will not be true. They will be trying to cover their asses. ...

What, if anything, can you do to prepare for this? Dr. Vanden Bossche is also very clear: “What I can advise. . . to all these vaccinated people: they need to avoid reinfection. It is the reinfection of vaccinated people that is responsible for this situation. . . . Well, the only thing they can do — it’s very simple — is take anti-virals, of course. The only difference is, you will not be able to wait to take anti-virals until you have symptoms. . . . As soon as people see that in one of the other countries, or one of the other states in the United States, when this starts with hospitalizations going up very rapidly, they need to take anti-virals prophylactically, not wait until they have any symptoms. I’m in Belgium. If it starts in the US, or starts in Israel, or starts in the UK, I bet you that within a few days, you will see the same scenario in many of the highly-vaccinated countries.”

By “anti-virals,” Dr. Vanden Bossche means specifically Ivermectin, the Nobel Prize-winning drug that the FDA and the CDC demonized brutally in order to distract the public from knowing that there was a safe and effective treatment for Covid. To acknowledge that would have vacated Pfizer’s and Moderna’s Emergency Use Authorization, which allowed them to make tens of billions of dollars on a very poorly tested pharma product while enjoying blanket protection against lawsuits. ...

Instead of ivermectin, US public health officials pushed the use of unsafe remdesivir with intubation, resulting in many thousands of avoidable deaths. This is only one of the crimes they will have to answer for.

If Dr. Vanden Bossche’s scenario comes to pass, the “hyper-acute Covid crisis” will intersect with the elections of 2024, and not just in the USA. You would naturally expect some extreme despotic hysterics out of the “Joe Biden” government. They will surely try to run their “Disease X” ruse. But they have already lost the trust of the people they made war against in their own country. In which case, expect resistance among the un-sick. No more trips will be laid on us.

Right, I'm also skeptical of that prediction.

It takes balls for Geert to make this prediction because it's coming. If no mass deaths occur by the end of this year, he'll lose credibility.

It takes balls for Geert to make this prediction because it's coming. If no mass deaths occur by the end of this year, he'll lose credibility.

porkchopXpress says

It takes balls for Geert to make this prediction because it's coming. If no mass deaths occur by the end of this year, he'll lose credibility.

You’re saying it’s coming also? You’re just not putting a time on it?

I have seen people wipe out their credibility over and over and over again, and they are still doing just fine.

It takes balls for Geert to make this prediction because it's coming. If no mass deaths occur by the end of this year, he'll lose credibility.

Why does it seem everyone in the UK is ill at present?

US is collaborating with Chinese scientists to make bird flu strains more infectious and deadly as part of $1m project - despite fears similar tests unleashed Covid

The US government is spending $1million of American taxpayer money to fund experiments on dangerous bird flu viruses in collaboration with Chinese scientists.

The research involves infecting ducks and geese with different strains of viruses to make them more infectious, and study the viruses' potential to 'jump into mammalian hosts,' according to research documents.

It is being funded through the US Department of Agriculture and collaborating studies will take place at sites in Georgia, Beijing and Edinburgh in Scotland.