So says a whopping 72% of Americans, according to a new Rasmussen Reports survey.



Onward and upward,
airforce

Cause of death? Kicking out James O'Keefe.



Onward and upward,
airforce

COVID-19 Vaccines Revealed To Be ‘Neither Safe, Nor Effective’: Watchdog

Authored by Naveen Athrappully via The Epoch Times (emphasis ours),

COVID-19 vaccines were authorized in Canada during 2020 and 2021 without being subjected to the country’s safety tests as required under established drug regulations, revealed an accountability watchdog.
A medical assistant holds a tray of syringes filled with doses of Moderna COVID-19 vaccine at a vaccination site in Los Angeles on Feb. 16, 2021. (Apu Gomes/AFP via Getty Images)

An investigation into COVID vaccines found that the jabs were “neither safe nor effective,” said the nonprofit National Citizens Inquiry (NCI) in a Sept. 15 post on X. The organization published a report Thursday detailing the flawed mechanism through which the vaccines were granted “approval” in Canada.

“It is important to understand that the COVID-19 vaccines were never approved under the traditional approval process for drugs in Canada,” stated the report (pdf). Instead, Health Canada, the federal agency responsible for national health policy, approved the vaccines through an alternative authorization process—an interim order.

“Under the alternative authorization process, the necessity to establish the safety and efficacy of COVID-19 vaccines through an objective manner appears to have been set aside.”

Canada’s Food and Drug Regulations require that a drug can only be approved in the country after its safety and effectiveness are demonstrated to the Minister of Health. Then, the minister considers whether the benefits outweigh the risks, following which, approval is granted.

Instead of following regulations, the Minister of Health sanctioned an interim order on Sept. 16, 2021, which exempted all COVID-19 vaccines from normal review and approval. This provision usually allows the minister to override normal regulations in situations of “significant risk” to health, safety, or the environment.

In Canada, four COVID-19 vaccines were authorized by the health agency under an interim order—Pfizer-BioNTech, Moderna, Janssen, and AstraZeneca.

The report noted that under the order, vaccines were authorized under a “subjective test.” In this situation, authorization is granted by simply proving that the benefits of vaccination outweigh the risks.

“This cannot be an appropriate standard for approving a drug that the Government intends to administer to the entire population. It is difficult to conceive of a less-scientific test for drug authorization than that found in the Interim Order.”

Moreover, the order made sure that the authorized vaccines could not be revoked even under evidence that it was unsafe and ineffective. Once an interim order is issued, the typical Food and Drug Regulations do not apply.

The order thus exempted manufacturers from having to effectively demonstrate “objective evidence of safety and effectiveness” of their COVID-19 vaccines.

“The result was that while chief medical officers across the country repeatedly assured Canadians that the COVID-19 vaccines were ‘safe and effective’—the general Canadian population had no understanding that their authorization process had not required objective proof of safety nor efficacy.”

‘Not Safe for Human Use’

The NCI report was supported by cardiologist Dr. Peter A. McCullough. “Excellent work @Inquiry_Canada with exhaustive testimony and evidence review. Conclusion: all COVID-19 vaccines unsafe for human use and must be removed from the Canadian market immediately to protect the public,” he wrote in a Sept. 16 post on X.
DALLAS, TX—Peter McCullough, cardiologist, speaks at the Conservative Political Action Conference in Dallas at the Hilton Anatole August 5, 2022. (Bobby Sanchez for The Epoch Times)

Dr. McCullough recently asked European lawmakers to take COVID-19 vaccines off the market due to concerns about illnesses like heart inflammation, blood clots, and neurological diseases.

“COVID-19 vaccines and all of their progeny and future boosters are not safe for human use. I implore you, as a governing body, European Medicines Agency (EMA), to apply all pressure and due urgency to remove the COVID-19 vaccines from market,” Dr. McCullough said in Sept. 13 testimony to the European Parliament.

The NCI report comes as the U.S. Food and Drug Administration (FDA) approved new COVID vaccines on Sept. 11 for children as young as six months old.

“Vaccination remains critical to public health and continued protection against serious consequences of COVID-19, including hospitalization and death,” Dr. Peter Marks, a top FDA official, said in a statement.

However, many experts have questioned the push for new vaccines. Earlier this month, Florida’s Surgeon General, Dr. Joseph Ladapo, criticized the updated shots.

“We all know there’s a new vaccine that’s coming around the corner, [a] new mRNA COVID-19 vaccine. And there’s essentially no evidence ‘for it,” he said during a press conference.

“There’s been no clinical trial done in human beings showing that it benefits people, there’s been no clinical trial showing that it is a safe product for people. And not only that, but then there are a lot of red flags.”

Mr. Ladapo said that mRNA COVID-19 vaccines have “caused cardiac injury in many people."

Not Actually ‘Interim’

Canada’s interim order for COVID-19 vaccines “has become permanent,” according to the NCI report (pdf). An interim order typically only lasts for one year. In March 2022, the order was replaced with permanent regulations which codified the “subjective authorization” of the vaccine.

“Thus, under the permanent test, Health Canada no longer has to be swayed by urgency, but simply by the public health need related to COVID-19. In this way, it seems that so long as COVID-19 is a circulating virus, Health Canada must authorize any vaccine for which there is an argument to support the conclusion that its benefits outweigh its risks,” the report said.

“In effect, we fear that there will never be a need for COVID-19 vaccine manufacturers to prove [the] safety or efficacy of their products.”

NCI also alleged there was a “conflict of interests” while approving the COVID-19 vaccines, with the government being involved.

Political Interests, Letter to Trudeau

Canada usually does not allow drugs to be imported into the country unless approved by Health Canada. However, the interim order allowed the unapproved COVID-19 vaccines to be imported “as long as the Canadian Government was the purchaser,” said the report.

This pre-purchasing and distribution of COVID vaccines were done to make sure the jabs were available for dissemination as soon as they were authorized. “This created a tremendous conflict of interest.”

“Once the vaccines were purchased, imported and ready for distribution, the Government of Canada would have suffered significant political blowback if it was unable to authorize them. Thus, it needed to authorize the COVID-19 vaccines, and it needed to do it quickly.”

The administration “ordered the vaccines, imported them, created new regulations to authorize them, and then took significant measures to convince and coerce every Canadian to take multiple doses. The political stakes were high, and the federal government had every motivation to get the vaccines authorized, regardless of their actual efficacy or safety.”

On Sept. 14, the NCI sent a letter (pdf) to Canadian Prime Minister Justin Trudeau highlighting the issue of COVID-19 vaccine approval.

“Canadians are relying on representations as to the safety and effectiveness of COVID-19 vaccines,” which Health Canada has never determined, the letter said. “Some might draw the conclusion that the misrepresentation to Canadians of proven safety is intentional, made while knowing it to be false and intending it to be relied upon.”

“As a matter of common sense, the objective falsity of the ‘proven safe’ claim brings into question the basis for informed consent to the administration of the injections, creating potentially enormous liabilities.”

In the current context, the organization pointed out that the population immunity has increased along with the latest variants being “milder.”

“In the face of your government’s reported intention to promote booster injections in coming months, the urgency now lies in telling the truth to Canadians and taking corrective action.”

The NCI asked the prime minister to withdraw COVID-19 vaccines “until the normal rigorous evaluation can be completed” and to reinstate the traditional objective test for safety.

The Death Of Informed Consent

Authored by Stella Paul via AmericanThinker.com,

Here’s what never happened in the hospital during COVID:

…a doctor sat down next to a patient and said,

“You have a choice.

We can give you Remdesivir, which killed 53% of the patients in an Ebola trial. It was so bad the trial had to be shut down. And you’ll notice here in Remdesivir’s fact sheet, it says, ‘Not a lot of people have used Remdesivir. Serious and unexpected side effects may happen.’

Or we can give you ivermectin, a safe and effective drug that’s been successfully used for decades, and send you home. Which do you prefer?”

The reason that conversation never happened is that it would have cost the hospital too much money. If the hospital gave you ivermectin and sent you home, the federal government paid the hospital $3,200. If the hospital gave you Remdesivir, the federal government paid the entire hospital bill, plus a 20% bonus. So the hospital executives’ choice was to receive $3,200 or $500,000, which was the average hospital bill. No contest. Patients were going to get Remdesivir — whether they wanted it or not.

Informed consent died a grotesque death in the hospitals during COVID, and we need an autopsy. There was no information, and there was no consent, and without them, patients are reduced to helpless victims, exploited for corrupt financial gain and immoral experiments.

Informed consent has been enshrined in numerous judicial rulings as the foundation of ethical medical practice and seared into the public’s conscience from the Nuremberg trials. Seven Nazi doctors were hanged in Germany by an American military tribunal for “murders, tortures, and other atrocities committed in the name of medical science.” Yet murders, tortures, and other atrocities are exactly what was committed by medical staff in the hospitals against thousands of Americans during COVID.

Take, for example, Ray Lamar, who arrived in the emergency room with a message written with a black sharpie pen on his arm: “NO VENT NO REMDESIVIR.” On his other arm, he wrote the same message and added his wife’s name and phone number. Yet the doctors gave him Remdesivir anyway, without ever informing him. His widow Patti told me she constantly wonders what she could have done to save him.

Image via Patti Lamar.

Christine Johnson told the doctors that she discussed all her medications with her daughter, who is a nurse, and she concluded that she didn’t want Remdesivir. It didn’t matter. Christine was given Remdesivir while she was sleeping, and now her daughter Michelle doesn’t have her mother.

Rebecca Stevens was an avid reader of Epoch Times, where she learned about Remdesivir’s dangers. She declined Remdesivir on five separate occasions, as her hospital records confirm. But the medical staff didn’t care what Rebecca wanted. She was given Remdesivir without her knowledge, and now Rebecca’s five grandsons are bereft.

I asked Michael Hamilton how it’s possible to give Remdesivir to patients without them knowing. Hamilton is a lawyer for several families who are suing California hospitals for the murder of their loved ones, and he’s heard thousands of victims’ stories.

“They would lie right to your face,” he said.

“You’d tell the nurse that you didn’t want Remdesivir and she’d say, ‘Fine. But you’re a bit dehydrated, so let’s get some fluids in you.’ And she’d hook up the IV, but it wasn’t fluids. It was Remdesivir.”

Hamilton told me that another favored tactic was to knock out patients with sedatives like morphine and fentanyl. While they lay there in a stupor, they were injected with Remdesivir.

If secret injections of Remdesivir weren’t enough to kill you, the hospitals had more torture lined up. After all, the federal government paid hospitals a big bonus to ventilate patients — so patients were going to get ventilated, whether they wanted to or not. A lot of patients turned down being vented, because the whole process is a nightmare. You’re painfully intubated, rendered unable to talk; your lungs start shredding, and you may acquire bacterial pneumonia, which the hospital will refuse to treat.

But “no” is not an acceptable answer when the hospital has money at stake. The medical staff’s preferred method for gaining “consent” was relentless bullying, screaming, coercion, and threats until the patient finally caved. Patti Lamar, Ray’s widow, told me that when she refused to let them ventilate her husband, the doctors screamed at her over and over, “You’re killing him! You’re killing him! You’re killing him!” When she couldn’t take it anymore, she reluctantly gave in. Ray died shortly thereafter, and Patti lives with the trauma of that moment.

Image via Dayna Stevens.

Michael Hamilton told me the fate of his friend who was a nurse, hospitalized in the place where she had worked for 26 years. When she refused ventilation, the doctor shrieked,

“You’re refusing medical advice! Now your insurance company won’t pay your hospital bill when you die! Do you want to bankrupt your family? Do you? Do you?” The nurse panicked, and to protect her family, she “consented.”

Two days later, she died.

“This was a very common technique,” Hamilton said.

“I’ve heard it hundreds of times. You tell the patient that unless they do what the doctor says, they’ll bankrupt their family because insurance won’t pay the hospital bills. Nobody wants to do that to their family.”

Does this sound like informed consent to you? It sounds more like medical battery to me.

The entire hospital environment was a hellscape of abuse in which informed consent wasn’t even a distant memory. Hamilton told me that patients were routinely denied all access to food and water, stupefied with 50 medications that included drugs contraindicated for each other, tortured with oxygen machines set at such high levels that they couldn’t breathe, and zip-tied to the bed till their wrists bled and their hands turned black. His stories align with 1,000 collected testimonies of the COVID-19 Human Betrayal Memory Project, which documents the victims’ fates.

The ultimate denial of informed consent was the hospitals’ refusal to allow the patients to leave.

“Patients lost all rights when they went in the hospital,” Senator Ron Johnson told Patty Myers in her documentary, Making A Killing.

“They became prisoners.”

A cottage industry of hospital rescues cropped up, as desperate family members hired lawyers to try to spring their loved ones out of hospital “care.” Ralph Lorigo, a lawyer in Buffalo, told me that in every case when he succeeded in getting a patient’s case before a judge and the judge ruled in the family’s favor, the patient went home and survived. In all cases where the judge refused to hear the case or ruled against the family, the patient died.

Every American is a sovereign individual with inalienable rights to life, liberty, and the pursuit of happiness, not a sack of meat to be treated as a profit opportunity. Informed consent must be revived from the grave if Americans are to have a fighting chance against powerful financial interests allied against them.

New ATF rule! They are coming for you!