Health
Ethical Vaccine: Trump nominee Jay Bhattacharya says NIH will not use aborted babies in research

Jayanta Bhattacharya, U.S. President Donald Trump’s nominee to be Director of the National Institutes of Health, speaks at his confirmation hearing before the Senate Committee on Health, Education, Labor, and Pensions on Capitol Hill
From LifeSiteNews
By Matt Lamb
The use of aborted babies in research is one of the main reasons many Christians oppose the use of several vaccines
The National Institutes of Health will not use abortion fetal tissue in research, according to President Donald Trump’s nominee to lead the agency.
Dr. Jay Bhattacharya made the comments on Wednesday during his hearing in front of the Senate Health, Education, Labor, and Pensions Committee in response to a question from Republican Senator Josh Hawley of Missouri.
“In public health, we need to make sure the products of science are ethically acceptable to everybody,” Bhattacharya said during the hearing. “And so having alternatives that are not ethically conflicted with fetal cell lines is not just an ethical issue, but it’s a public health issue.”
Dr. Bhattacharya said it is important to have ethical testing guidelines, sharing his experience answering questions on Catholic radio about the mRNA COVID shots. The jabs are tainted by their development using a fetal cell line derived from an aborted baby, which has caused moral concerns for faithful Catholics and also Protestants.
“Looking forward to voting for him to be our next NIH director,” Sen. Hawley wrote on X (formerly Twitter).
Dr. Bhattacharya is a well-respected medical doctor who gained further fame as a COVID contrarian, rejecting the establishment narrative that widespread lockdowns of the economy and schools were needed to slow the spread of the virus.
As LifeSiteNews previously reported:
Bhattacharya was one of the earliest and most notable critics of the draconian COVID response by most governments around the world. In October 2020 he co-authored The Great Barrington Declaration, which criticized the harmful lockdown policies. Bhattacharya is a professor of medicine, economics, and health research policy at Stanford University in California and the director of Stanford’s Center for Demography and Economics of Health and Aging.
Bhattacharya is the latest high-ranking public health official to affirm the Trump administration will not allow for the use of aborted fetal tissue in federally funded research.
Secretary of Health and Human Services Robert F. Kennedy Jr. previously assured Sen. Hawley he would prohibit the practice when questioned prior to his confirmation.
“Will you reinstate President Trump’s policy that ensures that no federal research and no federal tax dollars is conducted on fetal tissue taken from elective abortions,” Hawley asked RFK Jr.
“Yes,” the nominee said, as previously reported by LifeSiteNews.
President Trump’s administration previously rejected 13 or 14 requests to use aborted fetal tissue, as LifeSiteNews reported in 2020.
Business
Prime minister can make good on campaign promise by reforming Canada Health Act

From the Fraser Institute
While running for the job of leading the country, Prime Minister Carney promised to defend the Canada Health Act (CHA) and build a health-care system Canadians can be proud of. Unfortunately, to have any hope of accomplishing the latter promise, he must break the former and reform the CHA.
As long as Ottawa upholds and maintains the CHA in its current form, Canadians will not have a timely, accessible and high-quality universal health-care system they can be proud of.
Consider for a moment the remarkably poor state of health care in Canada today. According to international comparisons of universal health-care systems, Canadians endure some of the lowest access to physicians, medical technologies and hospital beds in the developed world, and wait in queues for health care that routinely rank among the longest in the developed world. This is all happening despite Canadians paying for one of the developed world’s most expensive universal-access health-care systems.
None of this is new. Canada’s poor ranking in the availability of services—despite high spending—reaches back at least two decades. And wait times for health care have nearly tripled since the early 1990s. Back then, in 1993, Canadians could expect to wait 9.3 weeks for medical treatment after GP referral compared to 30 weeks in 2024.
But fortunately, we can find the solutions to our health-care woes in other countries such as Germany, Switzerland, the Netherlands and Australia, which all provide more timely access to quality universal care. Every one of these countries requires patient cost-sharing for physician and hospital services, and allows private competition in the delivery of universally accessible services with money following patients to hospitals and surgical clinics. And all these countries allow private purchases of health care, as this reduces the burden on the publicly-funded system and creates a valuable pressure valve for it.
And this brings us back to the CHA, which contains the federal government’s requirements for provincial policymaking. To receive their full federal cash transfers for health care from Ottawa (totalling nearly $55 billion in 2025/26) provinces must abide by CHA rules and regulations.
And therein lies the rub—the CHA expressly disallows requiring patients to share the cost of treatment while the CHA’s often vaguely defined terms and conditions have been used by federal governments to discourage a larger role for the private sector in the delivery of health-care services.
Clearly, it’s time for Ottawa’s approach to reflect a more contemporary understanding of how to structure a truly world-class universal health-care system.
Prime Minister Carney can begin by learning from the federal government’s own welfare reforms in the 1990s, which reduced federal transfers and allowed provinces more flexibility with policymaking. The resulting period of provincial policy innovation reduced welfare dependency and government spending on social assistance (i.e. savings for taxpayers). When Ottawa stepped back and allowed the provinces to vary policy to their unique circumstances, Canadians got improved outcomes for fewer dollars.
We need that same approach for health care today, and it begins with the federal government reforming the CHA to expressly allow provinces the ability to explore alternate policy approaches, while maintaining the foundational principles of universality.
Next, the Carney government should either hold cash transfers for health care constant (in nominal terms), reduce them or eliminate them entirely with a concordant reduction in federal taxes. By reducing (or eliminating) the pool of cash tied to the strings of the CHA, provinces would have greater freedom to pursue reform policies they consider to be in the best interests of their residents without federal intervention.
After more than four decades of effectively mandating failing health policy, it’s high time to remove ambiguity and minimize uncertainty—and the potential for politically motivated interpretations—in the CHA. If Prime Minister Carney wants Canadians to finally have a world-class health-care system then can be proud of, he should allow the provinces to choose their own set of universal health-care policies. The first step is to fix, rather than defend, the 40-year-old legislation holding the provinces back.
COVID-19
FDA requires new warning on mRNA COVID shots due to heart damage in young men

From LifeSiteNews
Pfizer and Moderna’s mRNA COVID shots must now include warnings that they cause ‘extremely high risk’ of heart inflammation and irreversible damage in males up to age 24.
The Trump administration’s Food and Drug Administration (FDA) announced it will now require updated safety warnings on mRNA COVID-19 shots to include the “extremely high risk” of myocarditis/pericarditis and the likelihood of long-term, irreversible heart damage for teen boys and young men up to age 24.
The required safety updates apply to Comirnaty, the mRNA COVID shot manufactured by Pfizer Inc., and Spikevax, the mRNA COVID shot manufactured ModernaTX, Inc.
According to a press release, the FDA now requires each of those manufacturers to update the warning about the risks of myocarditis and pericarditis to include information about:
- the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 shots and
- the results of a study that collected information on cardiac magnetic resonance imaging (cardiac MRI) in people who developed myocarditis after receiving an mRNA COVID-19 injection.
The FDA has also required the manufacturers to describe the new safety information in the adverse reactions section of the prescribing information and in the information for recipients and caregivers.
Additionally, the fact sheets for healthcare providers and for recipients and caregivers for Moderna COVID-19 shot and Pfizer-BioNTech COVID-19 shot, which are authorized for emergency use in individuals 6 months through 11 years of age, have also been updated to include the new safety information in alignment with the Comirnaty and Spikevax prescribing information and information for recipients and caregivers.
In a video published on social media, Dr. Vinay Prasad, director of the Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, explained the alarming reasons for the warning updates.
While heart problems arose in approximately 8 out of 1 million persons ages 6 months to 64 years following reception of the cited shots, that number more than triples to 27 per million for males ages 12 to 24.
Prasad noted that multiple studies have arrived at similar findings.
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