Health
Cancer drug pioneer praises RFK Jr., suggests link between childhood cancer and COVID shots

From LifeSiteNews
Trump nominee for Secretary of Health and Human Services Robert F. Kennedy received a ringing endorsement from a medical pioneer, Dr. Patrick Soon-Shiong, who said the country needs to take seriously a possible link between the COVID-19 shots and childhood cancer.
Trump nominee for Secretary of Health and Human Services Robert F. Kennedy Jr. received a ringing endorsement from an acclaimed medical expert on Tuesday who said the country needs to take seriously a possible link between the COVID-19 shots and childhood cancer.
Dr. Patrick Soon-Shiong is a billionaire who pioneered the cancer drug Abraxane and has owned and led multiple medical companies. In 2018, he purchased the Los Angeles Times (which he blocked from endorsing Democrat Kamala Harris for president in 2024), and his ImmunityBio was among the companies recruited by the Trump administration to contribute to Operation Warp Speed.
On Tuesday, Soon-Shiong appeared on the 2WAY podcast, where he shared his thoughts about some of the big medical policy questions of the next four years.
“I think people misunderstand Bobby Kennedy, Robert F. Kennedy. He’s really all about the science,” he said. “I’ve sat down with him, met with him for the first time. I’ve not known him until I sat down with him, because I wanted to understand what he was thinking. And after hours of sitting down with him, I was so impressed. He knows more about the science than most doctors.”
Soon-Shiong went on to say “we’re going to have to address the rising incidence of cancer. For the first time in my career, I’ve seen an 8-year-old, 9-year-old, 10-year-old with colon cancer. The first time in my career, I’ve had a 13-year-old child in our clinic die of metastatic pancreatic cancer. We have to face this effectiveness and reality.”
The doctor ended on an optimistic note, saying that “there are effective therapies because we understand the science in such an immense way,” and adding that he is “excited about this next four years of bringing this information across and not to scare the population to say, look, we could lead the world in our innovation and using healthcare as a foreign policy around the world.”
A large body of evidence identifies significant risks to the COVID shots, which were developed and reviewed in a fraction of the time vaccines usually take under Operation Warp Speed.
The federal Vaccine Adverse Event Reporting System (VAERS) reports 38,264 deaths, 219,594 hospitalizations, 22,134 heart attacks, and 28,814 myocarditis and pericarditis cases as of December 27, among other ailments. CDC researchers have recognized a “high verification rate of reports of myocarditis to VAERS after mRNA-based COVID-19 vaccination,” leading to the conclusion that “under-reporting is more likely” than over-reporting.
An analysis of 99 million people across eight countries published in February in the journal Vaccine “observed significantly higher risks of myocarditis following the first, second and third doses” of mRNA-based COVID shots, as well as signs of increased risk of “pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis,” and other “potential safety signals that require further investigation.” In April, the CDC was forced to release by court order 780,000 previously undisclosed reports of serious adverse reactions, and a study out of Japan found “statistically significant increases” in cancer deaths after third doses of mRNA-based COVID-19 injections and offered several theories for a causal link.
Earlier this month, a long-awaited Florida grand jury report on the COVID shot manufacturers found that there were “profound and serious issues” in pharmaceutical companies’ review process, including reluctance to share what evidence of adverse events they found.
All eyes are currently on Trump and his health team, which will be helmed by Kennedy at HHS. As one of the country’s most vocal critics of the COVID establishment and vaccines more generally, his nomination brought hope that the second Trump administration will take a critical reassessment of the shots that the returning president has previously embraced, although most of Kennedy’s comments since joining Trump have focused on other issues, such as conventional vaccines and harmful food additives.
Trump has given mixed signals as to the prospects of reconsidering the shots and has nominated both critics and defenders of establishment COVID measures for a number of administration roles.
Aristotle Foundation
The Canadian Medical Association’s inexplicable stance on pediatric gender medicine

By Dr. J. Edward Les
The thalidomide saga is particularly instructive: Canada was the last developed country to pull thalidomide from its shelves — three months during which babies continued to be born in this country with absent or deformed limbs
Physicians have a duty to put forward the best possible evidence, not ideology, based treatments
Late last month, the Canadian Medical Association (CMA) announced that it, along with three Alberta doctors, had filed a constitutional challenge to Alberta’s Bill 26 “to protect the relationship between patients, their families and doctors when it comes to making treatment decisions.”
Bill 26, which became law last December, prohibits doctors in the province from prescribing puberty blockers and hormone therapies for those under 16; it also bans doctors from performing gender-reassignment surgeries on minors (those under 18).
The unprecedented CMA action follows its strongly worded response in February 2024 to Alberta’s (at the time) proposed legislation:
“The CMA is deeply concerned about any government proposal that restricts access to evidence-based medical care, including the Alberta government’s proposed restrictions on gender-affirming treatments for pediatric transgender patients.”
But here’s the problem with that statement, and with the CMA’s position: the evidence supporting the “gender affirmation” model of care — which propels minors onto puberty blockers, cross-gender hormones, and in some cases, surgery — is essentially non-existent. That’s why the United Kingdom’s Conservative government, in the aftermath of the exhaustive four-year-long Cass Review, which laid bare the lack of evidence for that model, and which shone a light on the deeply troubling potential for the model’s irreversible harm to youth, initiated a temporary ban on puberty blockers — a ban made permanent last December by the subsequent Labour government. And that’s why other European jurisdictions like Finland and Sweden, after reviews of gender affirming care practices in their countries, have similarly slammed the brakes on the administration of puberty blockers and cross-gender hormones to minors.
It’s not only the Europeans who have raised concerns. The alarm bells are ringing loudly within our own borders: earlier this year, a group at McMaster University, headed by none other than Dr. Gordon Guyatt, one of the founding gurus of the “evidence-based care” construct that rightfully underpins modern medical practice, issued a pair of exhaustive systematic reviews and meta analyses that cast grave doubts on the wisdom of prescribing these drugs to youth.
And yet, the CMA purports to be “deeply concerned about any government proposal that restricts access to evidence-based medical care,” which begs the obvious question: Where, exactly, is the evidence for the benefits of the “gender affirming” model of care? The answer is that it’s scant at best. Worse, the evidence that does exist, points, on balance, to infliction of harm, rather than provision of benefit.
CMA President Joss Reimer, in the group’s announcement of the organization’s legal action, said:
“Medicine is a calling. Doctors pursue it because they are compelled to care for and promote the well-being of patients. When a government bans specific treatments, it interferes with a doctor’s ability to empower patients to choose the best care possible.”
Indeed, we physicians have a sacred duty to pursue the well-being of our patients. But that means that we should be putting forward the best possible treatments based on actual evidence.
When Dr. Reimer states that a government that bans specific treatments is interfering with medical care, she displays a woeful ignorance of medical history. Because doctors don’t always get things right: look to the sad narratives of frontal lobotomies, the oxycontin crisis, thalidomide, to name a few.
The thalidomide saga is particularly instructive: it illustrates what happens when a government drags its heels on necessary action. Canada was the last developed country to pull thalidomide, given to pregnant women for morning sickness, from its shelves, three months after it had been banned everywhere else — three months during which babies continued to be born in this country with absent or deformed limbs, along with other severe anomalies. It’s a shameful chapter in our medical past, but it pales in comparison to the astonishing intransigence our medical leaders have displayed — and continue to display — on the youth gender care file.
A final note (prompted by thalidomide’s history), to speak to a significant quibble I have with Alberta’s Bill 26 legislation: as much as I admire Premier Danielle Smith’s courage in bringing it forward, the law contains a loophole allowing minors already on puberty blockers and cross-gender hormones to continue to take them. Imagine if, after it was removed from the shelves in 1962, government had allowed pregnant women already on the drug to continue to take thalidomide. Would that have made any sense? Of course not. And the same applies to puberty blockers and cross-gender hormones: they should be banned outright for all youth.
That argument is the kind our medical associations should be making — and would be making, if they weren’t so firmly in the grasp, seemingly, of ideologues who have abandoned evidence-based medical care for our youth.
J. Edward Les is a Calgary pediatrician, a senior fellow with the Aristotle Foundation for Public Policy, and co-author of “Teenagers, Children, and Gender Transition Policy: A Comparison of Transgender Medical Policy for Minors in Canada, the United States, and Europe.”
Health
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