COVID-19
Health researcher calls government promotion of Covid mRNA vaccines “confusing”

From (2079) Dr. John Campbell – YouTube
British Health researcher John Campbell has uncovered sobering and disturbing statistics regarding serious adverse events connected to covid vaccines.
As Campbell outlines in this presentation, multiple previous vaccines producing far fewer adverse events, have been withdrawn from public use while governments continue to promote covid vaccines.
(Campbell is well known for his meticulous research and he always includes links to the studies he is calling attention to. His presentation notes are below the video)
John Campbell’s research notes and links to relevant studies
Swine flu vaccine (1976), 1 serious event per 100,000 vaccinees,
Vaccine withdrawn Rotavirus vaccine
Rotashield, (1999),1 to 2 serious events per 10,000 vaccinees,
Vaccine withdrawn
Covid mRNA vaccines, 1 serious event per 800 vaccinees,
Vaccine officially promoted
Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults https://pubmed.ncbi.nlm.nih.gov/36055…
Free full text available https://www.ncbi.nlm.nih.gov/pmc/arti…
Why We Question the Safety Profile of mRNA COVID-19 Vaccines (Robert M Kaplan and Sander Greenland) https://sensiblemed.substack.com/p/wh…
Using publicly available data from Pfizer and Moderna studies, we found one serious adverse event for each 800 vaccinees. That translates to about 1,250 serious events for each million vaccine recipients.
US, Spain, Australia
Study to evaluate serious adverse events of special interest observed in mRNA COVID-19 vaccine trials.
Secondary analysis of serious adverse events reported in the placebo-controlled, phase III randomized clinical trials, of Pfizer and Moderna mRNA COVID-19 vaccines
Results Pfizer and Moderna mRNA COVID-19 vaccines were associated with an excess risk of serious adverse events
of special interest
Pfizer
10.1 per 10,000 vaccinated over placebo baselines of 17.6
Moderna
15.1 per 10,000 vaccinated over placebo baseline of 42.2
Combined, the mRNA vaccines Associated with an excess risk of serious adverse events of special interest of 12.5 per 10,000 vaccinated
Pfizer trial
Pfizer vaccine group 52 serious AESI (27.7 per 10,000) were reported
Pfizer placebo group 33 serious AESI (17.6 per 10,000) were reported
36 % higher risk of serious adverse events in the vaccine group
Risk difference 18.0 per 10,000 vaccinated
Moderna trial
Moderna trial, vaccine group 87 serious AESI (57.3 per 10,000) were reported
Moderna trial, placebo group 64 serious AESI (42.2 per 10,000) were reported
6 % higher risk of serious adverse events in the vaccine group
Risk difference 7.1 per 10,000 vaccinated
Discussion
The excess risk of serious adverse events found in our study points to the need for formal harm-benefit analyses, particularly those that are stratified according to risk of serious COVID-19 outcomes. These analyses will require public release of participant level datasets. Full transparency of the COVID-19 vaccine clinical trial data is needed, to properly evaluate these questions.
Unfortunately, as we approach 2 years after release of COVID-19 vaccines, participant level data remain inaccessible.
Level of adverse reactions in the past
The 1976 swine flu vaccine
Small increased risk of Guillain-Barré Syndrome
The increased risk was approximately 1 additional case of GBS for every 100,000 people who got the swine flu vaccine. When over 40 million people were vaccinated against swine flu, federal health officials decided that the possibility of an association of GBS with the vaccine, however small, necessitated stopping immunization until the issue could be explored.
The Institute of Medicine (2003) https://www.ncbi.nlm.nih.gov/books/NB…
Concluded that people who received the 1976 swine influenza vaccine had an increased risk for developing GBS. Exact reason for this association remains unknown.
Rotavirus vaccine Rotashield, (1999) https://www.cdc.gov/vaccines/vpd-vac/…
The U.S. Advisory Committee on Immunization Practices (ACIP) October 22, 1999 to no longer recommend use of the RotaShield® vaccine for infants, because of an association between the vaccine and intussusception. The results of the investigations showed that RotaShield® vaccine caused intussusception in some healthy infants Within 2 weeks Intussusception increased 20 to 30 times over the expected risk (Less after the second and third dose) CDC estimated that one or two additional cases of intussusception would be caused among each 10,000 infants vaccinated with RotaShield® vaccine.
2025 Federal Election
Mark Carney refuses to clarify 2022 remarks accusing the Freedom Convoy of ‘sedition’

From LifeSiteNews
Mark Carney described the Freedom Convoy as an act of ‘sedition’ and advocated for the government to use its power to crush the non-violent protest movement.
Canadian Prime Minister Mark Carney refused to elaborate on comments he made in 2022 referring to the anti-mandate Freedom Convoy protest as an act of “sedition” and advocating for the government to put an end to the movement.
“Well, look, I haven’t been a politician,” Carney said when a reporter in Windsor, Ontario, where a Freedom Convoy-linked border blockade took place in 2022, asked, “What do you say to Canadians who lost trust in the Liberal government back then and do not have trust in you now?”
“I became a politician a little more than two months ago, two and a half months ago,” he said. “I came in because I thought this country needed big change. We needed big change in the economy.”
Carney’s lack of an answer seems to be in stark contrast to the strong opinion he voiced in a February 7, 2022, column published in the Globe & Mail at the time of the convoy titled, “It’s Time To End The Sedition In Ottawa.”
In that piece, Carney wrote that the Freedom Convoy was a movement of “sedition,” adding, “That’s a word I never thought I’d use in Canada. It means incitement of resistance to or insurrection against lawful authority.”
Carney went on to claim in the piece that if “left unchecked” by government authorities, the Freedom Convoy would “achieve” its “goal of undermining our democracy.”
Carney even targeted “[a]nyone sending money to the Convoy,” accusing them of “funding sedition.”
Internal emails from the Royal Canadian Mounted Police (RCMP) eventually showed that his definition of sedition were not in conformity with the definition under Canada’s Criminal Code, which explicitly lists the “use of force” as a necessary aspect of sedition.
“The key bit is ‘use of force,’” one RCMP officer noted in the emails. “I’m all about a resolution to this and a forceful one with us victorious but, from the facts on the ground, I don’t know we’re there except in a small number of cases.”
Another officer replied with, “Agreed,” adding that “It would be a stretch to say the trucks barricading the streets and the air horns blaring at whatever decibels for however many days constitute the ‘use of force.’”
The reality is that the Freedom Convoy was a peaceful event of public protest against COVID mandates, and not one protestor was charged with sedition. However, the Liberal government, then under Justin Trudeau, did take an approach similar to the one advocated for by Carney, invoking the Emergencies Act to clear-out protesters. Since then, a federal judge has ruled that such action was “not justified.”
Despite this, the two most prominent leaders of the Freedom Convoy, Tamara Lich and Chris Barber, still face a possible 10-year prison sentence for their role in the non-violent assembly. LifeSiteNews has reported extensively on their trial.
COVID-19
17-year-old died after taking COVID shot, but Ontario judge denies his family’s liability claim

From LifeSiteNews
Ontario Superior Court Justice Sandra Antoniani ruled that the Department of Health had no ‘duty of care’ to individual members of the public in its pandemic response.
An Ontario judge dismissed a liability claim from a family of a high schooler who died weeks after taking the COVID shot.
According to a published report on March 26 by Blacklock’s Reporter, Ontario Superior Court Justice Sandra Antoniani ruled that the Department of Health had no “duty of care” to a Canadian teenager who died after receiving a COVID vaccine.
“The plaintiff’s tragedy is real, but there is no private law duty of care made out,” Antoniani said.
“There is no private law duty of care to individual members of the public injured by government core policy decisions in the handling of health emergencies which impact the general population,” she continued.
In September 2021, 17-year-old Sean Hartman of Beeton, Ontario, passed away just three weeks after receiving a Pfizer-BioNtech COVID shot.
After his death, his family questioned if health officials had warned Canadians “that a possible side effect of receiving a Covid-19 vaccine was death.” The family took this petition to court but has been denied a hearing.
Antoniani alleged that “the defendants’ actions were aimed at mitigating the health impact of a global pandemic on the Canadian public. The defendants deemed that urgent action was necessary.”
“Imposition of a private duty of care would have a negative impact on the ability of the defendants to prioritize the interests of the entire public, with the distraction of fear over the possibility of harm to individual members of the public, and the risk of litigation and unlimited liability,” she ruled.
As LifeSiteNews previously reported, Dan Hartman, Sean’s father, filed a $35.6 million lawsuit against Pfizer after his son’s death.
Hartman’s family is not alone in their pursuit of justice after being injured by the COVID shot. Canada’s Vaccine Injury Support Program (VISP) was launched in December 2020 after the Canadian government gave vaccine makers a shield from liability regarding COVID-19 jab-related injuries.
However, only 103 claims of 1,859 have been approved to date, “where it has been determined by the Medical Review Board that there is a probable link between the injury and the vaccine, and that the injury is serious and permanent.”
Thus far, VISP has paid over $6 million to those injured by COVID injections, with some 2,000 claims remaining to be settled.
According to studies, post-vaccination heart conditions such as myocarditis are well documented in those, especially young males who have received the Pfizer jab.
Additionally, a recent study done by researchers with Canada-based Correlation Research in the Public Interest showed that 17 countries have found a “definite causal link” between peaks in all-cause mortality and the fast rollouts of the COVID shots as well as boosters.
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