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Pfizer documents challenge Health Canada COVID-19 vaccine narrative

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7 minute read

From the Frontier Centre for Public Policy

By Ray McGinnis

Dr. Theresa Tam and senior federal health officials walked onto a stage this fall, socially distanced. Each wore masks, addressing an empty room.

Have they been living in a bubble?

The New York Times reported on February 21, 2023, that wearing masks did nothing to protect people from the COVID-19 virus.

Reporting on a rigorous and extensive study, Oxford epidemiologist Tom Jefferson said, “There is just no evidence that they [masks] make any difference. Full stop.” Jefferson said that even if one were to don an N-95 mask that it “makes no difference – none of it.” The microscopic hole in an N-95 mask was 35 microns. The much smaller droplet from the C-19 virus was 0.15 microns and could easily float through the N-19 mask hole. And why would a mask only be needed to protect us in public when we are not eating or drinking?

Health Canada continues to encourage the public to get COVID-19 boosters this fall. The agency asserts: “It’s considered safe to get both your COVID booster and a flu shot at the same appointment.” They are also “reviewing updated booster shots for children six months and up.”

However, release of the Pfizer Documents reveals people would be wise to avoid getting anymore boosters.

During its brief clinical trials, and in the first 12 weeks of the mRNA vaccine rollout, Pfizer compiled over 55,000 documents that related to clinical trials and other research the company conducted.  The company hoped these documents would be sealed from public view for 75 years.  The U.S. Food and Drug Administration supported keeping the data secret.

Nevertheless, a US court disagreed. The documents began being released in 2022. Steve K. Bannon hosted whistleblower Dr. Naomi Wolf on his War Room podcast. Together, they issued a call for medical and scientific experts to examine the documents. Project manager, Amy Kelly divided 3,500 highly trained specialists into teams. And they went through the material with a fine-toothed comb Their findings are published in the War Room/DailyClout Pfizer Documents Analysis Reports.

The teams learned that Pfizer had many reports of serious adverse events after the initial 12-week rollout – 158,000 – that they had to hire an additional 2,400 full-time staff to manage the caseload.

A Pfizer Safety Branch  Report concluded that by February 28, 2021, 1,223 people had died because of the vaccine.

Pfizer did not disclose all of its vaccine ingredients. In fact, a  news story reports: “Health Canada Confirms Undisclosed Presence of DNA Sequence in Pfizer Shot.” The Epoch Times explains that the Simian Virus 40 DNA sequence is in some of the the Pfizer mRNA vaccine, citing scientists who warn that it can be carcinogenic.

It seems that Pfizer kept sloppy records of the clinical trials. Pfizer Documents Investigation Team 5 reported: “a great deal of data… [is] missing from Pfizer’s analysis of adverse events that were reported after the Pfizer mRNA vaccine was approved by the US Food and Drug Administration…. The outcomes of almost one-quarter (22%) are not known.” They added, “Pfizer’s 3.7% fatality rate for the adverse event cases with known outcomes doesn’t include patients that Pfizer said had not recovered at the time of the report (30 April 2021).”

Team 1 reported that from December 1, 2020, “Pfizer was aware that the vaccine…had limited efficacy.” They reported that:“1,625 serious cases of vaccine ineffectiveness….” This included 136 people dying of COVID-19 related pneumonia after getting the Pfizer shot.

Team 3 examined what Pfizer did to ensure the safety of their vaccine. Did the vaccine stay in the arm, or did it travel to other places?

It was known that the engineered nanomaterials in the vaccine can cross or bypass the blood-brain barrier. What were the implications for the central nervous system? Team 3 discovered that: “This evaluation was never done in the Pfizer safety and efficacy trials… it is impossible to know whether the vaccine is safe in this arena. Pfizer did not prove the safety of the nano-lipid delivery system for the brain:” They just didn’t look under that rock.

In March 2022, the Journal of Pediatrics reported that the Seattle Children’s Hospital at the University of Washington had 35 cases of myocarditis in children within one week of receiving the second dose of the Pfizer vaccine. Team 1 reported that it was clear to both Pfizer and the FDA that by June 2021 there was a “serious problem of myocarditis in adolescents following mRNA vaccination….” Nonetheless, the FDA went ahead and issued the Emergency Use Authorization to include teenagers, and they did not mention the risks.

The Pfizer Documents also reveal that by February 28, 2021, they knew that serious stroke adverse events were occurring after vaccination. Pfizer observed 275 patients who had a stroke post-vaccine….“Strokes are life-altering events. Even Pfizer categorized all the reported stroke as serious.” Nonetheless, even after Pfizer examined the stroke adverse events, they offered an upbeat assessment: “This cumulative case review does not raise new safety issues.”

And what did Health Canada say?

Journalist Rodney Palmer reported to the National Citizens Inquiry that the Government of Canada reported that by “March 3, 2023, [there were] a total of 427 reports with an outcome of death…reported following vaccination.”

Unfortunately, Canadians are still living in a bubble with little understanding of the adverse effects of the COVID-19 vaccines and boosters.

 

Ray McGinnis is a senior fellow at the Frontier Centre for Public Policy, and author of Unanswered Questions and Writing the Sacred.

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‘They lied to us’: Wife of 53-year-old who died hours after receiving Remdesivir speaks out

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From LifeSiteNews

By Michael Nevradakis Ph. D., The Defender

Shannon is trying to raise public awareness of the COVID-19 hospital protocols that she believes led to her husband’s death.

In August 2021, 53-year-old Michael E. Pilgrim and his wife Shannon had just celebrated their 29th wedding anniversary and were looking forward to their daughter’s marriage in October.

A former military service member and father of two, Michael was a “good husband and great dad” and enjoyed golf in his spare time.

However, Michael’s fortunes dramatically changed that month when he experienced difficulty breathing and a low oxygen level. On Aug. 17, 2021, he was admitted to Dallas Regional Medical Center, near his hometown of Forney, Texas, with a COVID-19 diagnosis.

Two days later, on Aug. 19, he was dead.

In an interview with The Defender, Shannon Pilgrim said that from the time Michael was admitted to the hospital, she and other members of her family were barred from visiting him and kept in the dark about the treatment he was receiving.

READ: 26% of those prescribed Remdesivir for COVID died, according to Medicare database

According to Shannon, Michael’s medical records showed that doctors barely offered Michael any treatment and emphasized his unvaccinated status. Treatments Michael received included the controversial drug remdesivir — administered hours before his death.

Today, Shannon is trying to raise public awareness of the COVID-19 hospital protocols that she believes led to her husband’s death. She shared extensive medical documentation with The Defender corroborating her story.

‘Contradictory’ medical records contained ‘many gaps’

“The worst thing that’s ever happened to me is calling 911,” Shannon said. “I thought that I was doing the best thing for Michael. I came to find out that was the worst thing.”

Michael was taken to Dallas Regional Medical Center, a hospital that “has a horrible reputation” according to Shannon. She accused the hospital of refusing her request for Michael to be transferred and did not let her see him after he was admitted.

Shannon said communication with the hospital was limited. “I would call and the nurses would tell me they were on shift change or were busy and couldn’t talk to me.”

Doctors’ interactions with Michael were also limited, Shannon said. “They were just leaving him in a room and they had an iPad popped in to ask him about medical stuff.”

According to Shannon, most of what she’s learned about Michael’s treatment came from the medical records she obtained after his death — even though the records “are completely just contradictory” and contain “many gaps.”

Shannon referred to an instance when a Dallas Regional doctor told her that Michael was doing well — while the records indicate that the doctor called her to say Michael was in critical condition.

Shannon said the records revealed that the hospital “did nothing” for Michael. She said:

On the first day, they basically didn’t do anything except give him oxygen. The next day, he had a chest X-ray and then doctors gave him vitamins … there’s contradictory stuff in here about whether he even had an IV. I can’t even get — from looking at his medical records — if they gave him fluid.

They started giving him Lovenox shots for blood clots. Why? He didn’t have blood clots … Then they started giving him insulin. Why were they giving him insulin? He wasn’t a diabetic.

But according to the medical records, they really didn’t do anything, and that’s what just completely floored me — except they gave him remdesivir.

Remdesivir, which has been linked to deaths and injuries in COVID-19 patients, was commonly administered to patients under the COVID-19 hospital protocols.

According to Shannon, the records indicate that Michael was administered remdesivir on the day of his death. But as she recalls, when she spoke to her husband on the phone that day at noon he showed no signs of being in danger.

“He called me, and I actually got to talk to him. I didn’t talk to him very long, but he wasn’t on a ventilator. He was better,” Shannon said. “I called my kids and I was like, ‘He sounded so good.’ I said, ‘He’s going to be coming home.’ I was so excited.”

Yet, that afternoon, Michael was given remdesivir. According to Shannon, the hospital called her a few hours later to say that Michael was found unresponsive.

“I got hysterical,” Shannon said. “I was asking again and again, ‘Is he OK? Where is he? How do I get in touch?’ … She wouldn’t give me her name. She just said, ‘I’m so sorry.’ She said he coded and they took him to ICU and ‘someone will call you tomorrow’ … And she hung up the phone on me.”

Shannon’s son called Dallas Regional and was told Michael had died. But the family’s difficulties did not end there, as the hospital did not allow them to see Michael’s body.

“We didn’t get to see him until he was embalmed, because they told us that he had COVID,” Shannon said.

Shannon said she believes her husband’s unvaccinated status played a role in the treatment he received. She said Michael had been “cautious” about the COVID-19 vaccine and reluctant to receive it — and that the hospital was aware of this.

“You see all through his medical records, ‘unvaccinated,’ ‘unvaccinated,’ ‘unvaccinated,’” Shannon said. “It’s even written in there, ‘doesn’t trust the vaccine.’”

‘They completely lied’

Shannon said the hospital stonewalled her and her family after Michael’s death.

“They wouldn’t talk to me, they wouldn’t take my calls,” Shannon said. “I kept calling up there and begging to have somebody tell me what happened and nobody would tell me.” The hospital then started pursuing her for unpaid medical bills, she said.

When she did speak to hospital personnel, they misled her. In one instance, she said a doctor told her that while she had the right to have an autopsy performed on Michael’s body, local authorities were “six to eight months behind” and that she’d have to wait that long for the body to be released.

“They completely lied, because later I found out that by law they have to do an autopsy within two weeks, and then it can be six to eight months before you actually get the report. But they have to do it and they have to release the body. But they lied to us and we trusted them,” Shannon said.

Instead, Shannon said the government-funded COVID-19 Bereavement Assistance Fund offered a $10,000 payout for Michael’s death. “They were giving up to $10,000 if the death certificate had COVID on it. And I said, ‘no way in hell will I take that payout.”

Instead, Shannon became an advocate for families that endured similar experiences, by joining the FormerFedsGroup Freedom Foundation. Through her involvement with this advocacy group, Shannon has met with legislators, attorneys and family members of other COVID-19 hospital protocol victims.

“It’s hard, but I don’t want other loved ones to go through what we went through,” Shannon said. “I realized that I want to keep fighting. And so, as hard as it is to keep reliving this timeframe, I will keep doing it … I don’t want people to think he died from COVID, because he didn’t. He died at the hospital because of them. They killed him.”

 

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

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Media failing to cover ‘powerful testimony’ of people injured by COVID vaccines

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From LifeSiteNews

By Brenda Baletti, Ph.D., The Defender

Kate Scott’s husband Jamie was an athlete, a high-power executive, and an active husband and father of two boys until he nearly died after experiencing jab-induced immune thrombosis and thrombocytopenia from the AstraZeneca COVID shot.

Important information coming out of the ongoing UK Covid-19 Inquiry is “slipping between the cracks” of media coverage, YouTube commenter John Campbell, Ph.D., reported on a recent episode of his show.

Campbell played clips of testimony by Kate Scott, who represents the U.K.’s Covid Vaccine Injured & Bereaved (VIBUK). Kate’s husband, Jamie, suffered a traumatic brain injury and was left severely disabled by the AstraZeneca vaccine.

Kate’s testimony is part of the inquiry’s fourth module, investigating issues related to the COVID-19 shots and therapeutics.

Jamie was an athlete, a high-power executive, and an active husband and father of two boys until he nearly died after experiencing jab-induced immune thrombosis and thrombocytopenia. He was in a coma for four weeks and five days.

Jamie survived, Kate explained, but his life will never be the same. His traumatic brain injury affects his thinking processes and his emotions. He is partially blind and he will never be able to work again, to live independently, or to look after their children.

Kate said that she and her group were testifying to draw attention to the fact that many people were injured by the shot, to remove the stigma of jab injuries, and to compel the government and pharmaceutical companies “to look again at how to deal with the inconvenient fact of vaccine injury and bereavement and the lives it has shattered.”

She said the very first serious side effects from the AstraZeneca shot “should have rung an alarm with the MHRA” – Medicines and Healthcare products Regulatory Agency – and the U.K. “government that there was a serious problem. However, no action was taken.”

She presented data that VIBUK obtained via a freedom of information law request showing that, as of November 30, 2024, 17,519 vaccine injury victims have made claims to the government’s Vaccine Damage Payment scheme.

Of those, she said, only 194 victims have been notified that they are entitled to payment, and only 55 have received any payment. The maximum allowed payment is 120,000 pounds (approximately $150,000).

Kate also revealed that people are deemed ineligible for compensation if they are considered less than 60 percent disabled and that many people receive diagnoses that they are 59 percent disabled.

“A percentage disablement is also somewhat offensive,” she said. “Regardless of if it’s 10 percent or 59 percent or, Jamie, way over 60 percent, or dead — I guess that’s 100% disabled — there’s no compensation if you fall below that [60 percent].”.

“The consequence of being told, ‘sorry you’re only 55% disabled,’ it’s awful, it’s devastating and then there’s nothing for you, no one to help.”

Commenting on her testimony, Campbell asked, “How on earth can a clinician adjudicate someone is only 59 percent disabled? Why not 58? Why not 61? How can you be 59 percent disabled? I don’t understand that. I simply don’t understand it.”

Kate added, “Statistics are interesting, aren’t they? Within our group, [for] 100 percent of the people in it, [the vaccine] was not ‘safe and effective.’”

The group recommended that pharmaceutical companies should not fund the government agencies that regulate them. They also said the Yellow Card scheme — which is the U.K.’s adverse events reporting system for medicines, vaccines, medical devices and other products — should be mandatory rather than voluntary.

Kate also said the government should follow up when people file yellow cards. Many people in their group had filed cards, but no one ever contacted them to investigate.

“We are important,” she said. “We’re part of this pandemic story.”

Campbell asked, “Why is it that so many things only come to light from freedom of information requests?” He said it’s a pity these stories are not being picked up by the media. “Powerful testimony, not well-covered, unfortunately,” he said.

Watch here:

Republished with permission from Children’s Health Defense – Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

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