Science
Trump Administration Temporarily Mutes Federal Health Officials
The Trump administration, moving quickly to clamp down on health and science agencies, has canceled a string of scientific meetings and instructed federal health officials to refrain from all public communications, including upcoming reports focused on the nation’s escalating bird flu crisis.
Experts who serve on outside advisory panels on a range of topics, from antibiotic resistance to deafness, received emails on Wednesday telling them their meetings had been canceled.
The cancellations followed a directive issued on Tuesday by the acting director of the federal Department of Health and Human Services, who prohibited the public release of any public communication until it had been reviewed by a presidential appointee or designee, according to federal officials and an internal memo reviewed by The New York Times.
The directive enjoins the public release of “regulations, guidance documents, and other public documents and communications,” including any “notice,” “grant announcement,” news releases, speaking engagements or official correspondence with public officials, until they have received approval.
The new stricture applies to messages to email groups and to social media posts, and included a ban on announcements to The Federal Register, without which many official processes cannot continue. Some notices sent by the Biden administration in its final week were quickly withdrawn.
The cancellations and communications crackdown sent a chill through employees of the Centers for Disease Control and Prevention and the broader scientific community. The directive was first reported by The Washington Post.
Representatives of the C.D.C. and the Food and Drug Administration declined to comment. The moratorium is to continue through Feb. 1.
The fallout was immediate.
Officials at the C.D.C. had been prepared to publish an issue of the influential Morbidity and Mortality Weekly Report on Thursday that included several items related to the widening bird flu outbreak on dairy and poultry farms.
The weekly reports have been called the “holiest of the holy,” a crucial means of communication about developments in public health. This week’s publication is now held up as a result of the order, according to two federal health officials who spoke on condition of anonymity because they were not authorized to speak publicly.
Upcoming meetings of outside advisory panels on health issues have been canceled, according to panel members, who spoke anonymously for fear of retribution. Meetings to review grant proposals submitted to the National Institutes of Health were scrubbed, for example.
Members of the Presidential Advisory Council for Combating Antibiotic-Resistant Bacteria were told that their two-day meeting, scheduled for next Tuesday and Wednesday, had been canceled “as the new Administration considers its plan for managing federal policy and public communications.”
Those who had registered in advance for a celebratory dinner were told they would be “fully reimbursed within 48 hours” of receiving the email.
The directive was signed by Dr. Dorothy Fink, acting secretary of the Department of Health and Human Services. The confirmation hearing for Robert F. Kennedy Jr., whom President Trump has nominated to lead the department, is not expected for at least another week.
The administration has yet to name an acting director for the C.D.C. or an acting commissioner at the Food and Drug Administration, usually among the first moves by an incoming administration.
The communications pause accompanies a spate of other changes facing federal employees since Mr. Trump’s inauguration on Monday, including a hiring freeze, an end to remote work and the shuttering of diversity, equity and inclusion offices and programs.
Late on Wednesday, Dr. Fink issued another directive aimed at ending diversity and inclusion efforts at H.H.S. and warned against attempting to “disguise these programs by using coded or imprecise language.” Her letter also encouraged employees to report on colleagues who were not compliant.
Former federal officials said it was not unusual for a new administration to limit communication during the initial transition, but the scope and duration of the latest pause were unexpected.
Staff members of the incoming Trump administration did not use the transition period to meet with federal health officials and to familiarize themselves with the agencies.
And while a pause on communications is not out of the ordinary, previous administrations have not restricted scientific publications like the M.M.W.R. or health guidelines because of their critical importance to public welfare.
“It’s not unusual for a new administration to want to centralize communication,” said Dr. Richard Besser, the chief executive of the Robert Wood Johnson Foundation and a former acting director of the C.D.C.
“It is unusual to pause all communication from an agency where one of its critical responsibilities is keeping the public informed,” he added.
Privately, several federal officials said they were confused about whether the restriction on communications with The Federal Register included health data. Some officials seemed unaware of the restrictions at all.
Much of the concern centered on the C.D.C., whose responsibilities certainly include public communications. The agency, for example, recently made doctors and patients aware of potential health risks about an emerging version of mpox and an outbreak of Marburg disease in Rwanda.
The agency has offered findings on the mental health effects of the pandemic on health care providers and new guidelines extending the recommendation for pneumococcal vaccines, and has warned of an increase in the incidence of tularemia, a rare infectious disease, in the United States.
State and city health officials rely on C.D.C. notices to make decisions for their communities, such as when to ramp up flu testing or which disease symptoms to keep an eye out for, said Chrissie Juliano, executive director of the Big Cities Health Coalition, which represents leaders of urban public health departments.
While much of that information can be delayed a few days, she said she hoped that the administration had a plan for disseminating more pressing public health information, especially in relation to the bird flu outbreak.
In the past year, the bird flu virus, called H5N1, has affected dozens of animal species and more than 35 million wild and commercial birds, resulting in soaring egg prices. It has also infected at least 67 people; the country recorded its first bird-flu-related human death in December.
“Can something like the bird flu turn on a dime in 10 days?” Ms. Juliano said. “Yes. I would hope that if those signals are seen at the federal level, information is going to get out.”
Dr. Ashish Jha, dean of the Brown University School of Public Health and the Biden administration’s former Covid czar, said the pause on communications was most likely a product of the Trump administration’s “particularly bumpy” transition into the White House, rather than a coordinated effort to withhold information.
Still, public health experts are wary of any changes to access of federal health data. Memories from Mr. Trump’s last term, during which political appointees repeatedly meddled in C.D.C. reports and doctored guidance documents, are still raw.
“I think if it goes anywhere beyond Feb. 1, then we have a much more serious problem,” Dr. Jha said.
Science
What’s in a Name? For These Snails, Legal Protection
The sun had barely risen over the Pacific Ocean when a small motorboat carrying a team of Indigenous artisans and Mexican biologists dropped anchor in a rocky cove near Bahías de Huatulco.
Mauro Habacuc Avendaño Luis, one of the craftsmen, was the first to wade to shore. With an agility belying his age, he struck out over the boulders exposed by low tide. Crouching on a slippery ledge pounded by surf, he reached inside a crevice between two rocks. There, lodged among the urchins, was a snail with a knobby gray shell the size of a walnut. The sight might not dazzle tourists who travel here to see humpback whales, but for Mr. Avendaño, 85, these drab little mollusks represent a way of life.
Marine snails in the genus Plicopurpura are sacred to the Mixtec people of Pinotepa de Don Luis, a small town in southwestern Oaxaca. Men like Mr. Avendaño have been sustainably “milking” them for radiant purple dye for at least 1,500 years. The color suffuses Mixtec textiles and spiritual beliefs. Called tixinda, it symbolizes fertility and death, as well as mythic ties between lunar cycles, women and the sea.
The future of these traditions — and the fate of the snails — are uncertain. The mollusks are subject to intense poaching pressure despite federal protections intended to protect them. Fishermen break them (and the other mollusks they eat) open and sell the meat to local restaurants. Tourists who comb the beaches pluck snails off the rocks and toss them aside.
A severe earthquake in 2020 thrust formerly submerged parts of their habitat above sea level, fatally tossing other mollusks in the snail’s food web to the air, and making once inaccessible places more available to poachers.
Decades ago, dense clusters of snails the size of doorknobs were easy to find, according to Mr. Avendaño. “Full of snails,” he said, sweeping a calloused, violet-stained hand across the coves. Now, most of the snails he finds are small, just over an inch, and yield only a few milliliters of dye.
Science
Video: This Parrot Has No Beak, But Is at the Top of the Pecking Order
new video loaded: This Parrot Has No Beak, But Is at the Top of the Pecking Order
By Meg Felling and Carl Zimmer
April 20, 2026
Science
Contributor: Focus on the real causes of the shortage in hormone treatments
For months now, menopausal women across the U.S. have been unable to fill prescriptions for the estradiol patch, a long-established and safe hormone treatment. The news media has whipped up a frenzy over this scarcity, warning of a long-lasting nationwide shortage. The problem is real — but the explanations in the media coverage miss the mark. Real solutions depend on an accurate understanding of the causes.
Reporters, pharmaceutical companies and even some doctors have blamed women for causing the shortage, saying they were inspired by a “menopause moment” that has driven unprecedented demand. Such framing does a dangerous disservice to essential health advocacy.
In this narrative, there has been unprecedented demand, and it is explained in part by the Food and Drug Administration’s recent removal of the “black-box warning” from estradiol patches’ packaging. That inaccurate (and, quite frankly, terrifying) label had been required since a 2002 announcement overstated the link between certain menopause hormone treatments and breast cancer. Right-sizing and rewording the warning was long overdue. But the trouble with this narrative is that even after the black-box warning was removed, there has not been unprecedented demand.
Around 40% of menopausal women were prescribed hormone treatments in some form before the 2002 announcement. Use plummeted in its aftermath, dipping to less than 5% in 2020 and just 1.8% in 2024. According to the most recent data, the number has now settled back at the 5% mark. Unprecedented? Hardly. Modest at best.
Nor is estradiol a new or complex drug; the patch formulation has existed for decades, and generic versions are widely manufactured. There is no exotic ingredient, no rare supply chain dependency, no fluke that explains why women are suddenly being told their pharmacy is out of stock month after month.
The story is far more an indictment of the broken insurance industry: market concentration, perverse incentives and the consequences of allowing insurance companies to own the pharmacy benefit managers that effectively control drug access for the majority of users. Three companies — CVS Caremark, Express Scripts and OptumRx — manage 79% of all prescription drug claims in the United States. Those companies are wholly owned subsidiaries of three insurance behemoths: CVS Health, Cigna and UnitedHealth Group, respectively. This means that the same corporation that sells you your insurance plan also decides which drugs get covered, at what price, and whether your pharmacy can stock them. This is called vertical integration. In another era, we might have called it a cartel. The resulting problems are not unique to hormone treatments; they have affected widely used medications including blood thinners, inhalers and antibiotics. When a low-cost generic such as estradiol — a medication with no blockbuster profit margins and no patent protection — runs into friction in this system, the friction is not random. It is structural. Every decision in that chain is filtered through the same corporate profit motive. And when the drug in question is an off-patent estradiol patch that has negligible profit margins because of generic competition but requires logistical investment to keep consistently in stock? The math on “how much does this company care about ensuring access” is not complicated.
Unfortunately, there is little financial incentive to ensure smooth, consistent access. There is, however, significant financial incentive to steer patients toward branded alternatives, or simply to let supply tighten — because the companies aren’t losing much profit if sales of that product dwindle. This is not a conspiracy theory: The Federal Trade Commission noted this dynamic in a report that documented how pharmacy benefit managers’ practices inflate costs, reduce competition and harm patient access, particularly for independent pharmacies and for generic drugs.
Any claim that the estradiol patch shortage is meaningfully caused by more women now demanding hormone treatments is a distraction. It is also misogyny, pure and simple, to imply that the solution to the shortage is for women’s health advocates to dial it down and for women to temper their expectations. The scarcity of estradiol patches is the outcome of a broken system refusing to provide adequate supply.
Meanwhile, there are a few strategies to cope.
- Ask your prescriber about alternatives. Estradiol is available in multiple formulations, including gel, spray, cream, oral tablet, vaginal ring and weekly transdermal patch, which is a different product from the twice-weekly patch and may be more consistently available depending on manufacturer and region.
- Consider an online pharmacy. Many are doing a good job locating and filling these prescriptions from outside the pharmacy benefit manager system.
- Call ahead. Patch shortages are inconsistent across regions and distributors. A call to pharmacies in your area, or a broader geographic radius if you’re able, can locate stock that your regular pharmacy doesn’t have.
- Consider a compounding pharmacy. These sources can sometimes meet needs when commercially manufactured products are inaccessible. The hormones used are the same FDA-regulated bulk ingredients.
Beyond those Band-Aid solutions, more Americans need to fight for systemic change. The FTC report exists because Congress asked for it and committed to legislation that will address at least some of the problems. The FDA took action to change the labeling on estrogen in the face of citizen and medical experts’ pressure; it should do more now to demand transparency from patch manufacturers.
Most importantly, it is on all of us to call out the cracks in the current system. Instead of repeating “there’s a patch shortage” or a “surge in demand,” say that a shockingly small minority of menopausal women still even get hormonal treatments prescribed at all, and three drug companies control the vast majority of claims in this country. Those are the real problems that need real solutions.
Jennifer Weiss-Wolf, the executive director of the Birnbaum Women’s Leadership Center at New York University School of Law, is the author of the forthcoming book “When in Menopause: A User’s Manual & Citizen’s Guide.” Suzanne Gilberg, an obstetrician and gynecologist in Los Angeles, is the author of “Menopause Bootcamp.”
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