CDC

RFK Jr. drags feet on COVID-19 vaccine recommendations, delaying shots for kids

ACIP, CDC, COVID-19 vaccines, health, robert f kennedy jr, vaccines / Mike M. / October 3, 2025

Previously, the FDA narrowed the shots’ labels to include only people age 65 and older, and those 6 months and older at higher risk. But the ACIP recommended that all people age 6 months and older could get the shot based on shared decision-making with a health care provider. Although the shared decision-making adds a new requirement for getting the vaccine, that decision-making does not require a prescription and can be done not only with doctors, but also with nurses and pharmacists. Most people in the US get their seasonal COVID-19 vaccines at their local pharmacy.

Ars Technica reached out to the HHS on Thursday about whether there was a determination on the COVID-19 vaccine recommendations and, if not, when that is expected to happen and why there is a delay. The HHS responded, confirming that no determination had been made yet, but did not answer any of the other questions and did not provide a comment for the record.

In past years, ACIP recommendations and CDC sign-offs have happened earlier in the year to provide adequate time for a rollout. In 2024, ACIP voted on COVID-19 vaccinations in June, for instance, and then-CDC Director Mandy Cohen signed off that day. Now that we’re into October, it remains unclear when or even if the CDC will sign off on the recommendation and then, if the recommendation is adopted by the CDC, how much longer after that it would take for states to roll out the vaccines to children in the VFC program.

“Children who depend on this program, including children with chronic conditions, are still waiting unprotected. The delay in adopting COVID-19 vaccine recommendations puts their health at risk, reduces access and choice for families, and puts a strain on providers who want to deliver the best care for their youngest patients,” Susan Kansagra, the chief medical officer of the Association of State and Territorial Health Officials, said in a statement to Stat.

For now, children and adults with private insurance have access to the shots without the final sign-off, and health insurance companies have said that they will continue to maintain coverage for the vaccines without the final federal approval.

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In 2022, the world axed a disease name seen as racist. US just switched back.

CDC, health, mpox, Trump / 9u50fv / October 1, 2025

Switching names

In November 2022, the WHO decided to change the name. The United Nations health agency noted that it had received reports from individuals and countries about the “racist and stigmatizing language online, in other settings, and in some communities.” The WHO decided to switch to the name “mpox” with a one-year grace period.

The agency also clarified its authority to make such a change, saying: “Assigning names to new and, very exceptionally, to existing diseases is the responsibility of WHO under the International Classification of Diseases (ICD) and the WHO Family of International Health Related Classifications through a consultative process which includes WHO Member States.”

The WHO does not, however, have the authority to change the names of viruses. That power belongs to the International Committee on Taxonomy of Viruses, which has not changed the name of the virus.

While the virus remains the same, the world has shifted to using mpox to discuss the disease. The US CDC followed suit, changing its websites and health information to use the new name.

This month, however, the CDC reverted to monkeypox. The change was first reported by NPR. When journalists have asked about the change, the Department of Health and Human Services (which includes the CDC) has responded only by saying “Monkeypox is the name of the viral disease caused by the monkeypox virus,” which is not accurate.

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RFK Jr.’s anti-vaccine panel realizes it has no idea what it’s doing, skips vote

ACIP, CDC, health, hepatitis B, Rober F. Kennedy Jr., vaccine / DJ Henderson / September 19, 2025

With a lack of data and confusing language, the panel tabled the vote indefinitely.

Catherine Stein, far right, speaks during a meeting of the CDC’s Advisory Committee on Immunization Practices on September 18, 2025 in Chamblee, Georgia. Credit: Getty | Elijah Nouvelage

The second day of a two-day meeting of the Advisory Committee on Immunization Practices—a panel currently made up of federal vaccine advisors hand-selected by anti-vaccine activist Robert F. Kennedy, Jr.—is off to a dramatic start, with the advisors seemingly realizing they have no idea what they’re doing.

The inexperienced, questionably qualified group that has espoused anti-vaccine rhetoric started its second day of deliberations by reversing a vote taken the previous day on federal coverage for the measles, mumps, rubella, and varicella (MMRV) vaccine. Yesterday, the group voted to restrict access to MMRV, stripping recommendations for its use in children under age 4. While that decision was based on no new data, it passed with majority support of 8–3 (with one abstention). (For an explanation of that, see our coverage of yesterday’s part of the meeting here.)

But puzzlingly, they then voted to uphold access and coverage of MMRV vaccines for children under age 4 if they receive free vaccines through the federal Vaccines for Children program, which covers about half of American children, mostly low-income. The discrepancy projected the idea that the alleged safety concerns that led the panel to rescind the recommendation for MMRV generally, somehow did not apply to low-income, vulnerable children. The vote also created significant confusion for VFC coverage, which typically aligns with recommendations made by the panel.

Today, Kennedy’s ACIP retook the vote, deciding 9-0 (with three abstentions) to align VFC coverage with their vote yesterday to strip the recommendation for MMRV in young children.

Hepatitis B vaccine newborn dose

Next, they moved to a vote they failed to take yesterday as scheduled—a vote to strip a recommendation for a dose of hepatitis B vaccine that is currently recommended to be given universally on the first day of a baby’s life. Instead, the proposed recommendation would be to wait at least a month before the first dose—opening a window for a highly infectious disease that leads to chronic liver disease and cancer—unless the baby’s mother tested positive for the virus.

While it initially seemed that the panel was poised to approve the change, cracks in the plan began to appear quickly this morning, as some members of the panel noted that the proposed recommendation made no sense and was based on zero data.

Joseph Hibbeln, a psychiatrist on the panel, raised the obvious concern yesterday, saying: “I’m unclear if we’ve been presented with any safety or data comparing before one month to after one month, and I’m wondering why one month was selected as our time point and if there are data to help to inform us if there’s greater risk of adverse effects before one month or after one month at all, let alone in negative mothers.”

There was no data comparing the risks and benefits of moving the first dose from the day of birth to any other time point. And there is no data suggesting that such a move would be more or less safe.

Adam Langer, Acting Principal Deputy Director of the CDC’s National Center for HIV, Viral Hepatitis, STD, and Tuberculosis Prevention, stressed in his presentation on the safety data yesterday, that the vaccine is safe—there are no safety concerns for giving a dose at birth. Adverse side effects are rare, he said, and when they do occur, they’re mild. “The worst adverse event you could imagine, anaphylaxis, has been very rarely reported at only 1.1 cases per 1 million vaccine doses administered.”

Langer gave a clear explanation for why newborns are vaccinated at day one. Hepatitis B, which primarily affects the liver, spreads via bodily fluids and can live on surfaces for up to seven days. It can spread easily; only a tiny microscopic amount of blood or fluid is enough for a child to be infected. For some, an infection can be short-lived, but for others it can become chronic, which leads to liver disease, cirrhosis, liver transplant, and liver cancer. The risk of the infection becoming chronic increases with the younger someone is when they’re infected.

Benefits and harms

Newborns who get hepatitis B from their mothers at birth have a 90 percent chance of developing a chronic infection, and 25 percent of those children will die prematurely from the disease. Up to 16 percent of pregnant women in the US are not tested for hepatitis B during pregnancy. Newborns and babies can also get infected from other people in their family or household, given hepatitis B’s infectiousness. Prior to the universal birth dose recommendation, a study of US-born children born to immigrant mothers found that 7 percent to 11 percent of them had hepatitis B while their mothers were negative. This highlights that unvaccinated babies and children can pick up the infection from family or the community.

Part of the reason for this is the elusiveness of the disease. While about 2.4 million people in the US are infected with hepatitis B, about 50 percent of those infected do not know that they’re infected.

In 1991, ACIP began recommending universal hepatitis B vaccination at birth; acute hepatitis B cases then fell from around 18,000 to about 5,500 in 2005 to about 2,200 in 2023. Since 2018, ACIP has recommended universal Hep B vaccination for all newborns within 24 hours of birth.

In the discussion, panel members pushed back on the universal birth dose, arguing that if mothers tested negative, there was little to no risk—downplaying the risk of other family or community exposure and assuming that test coverage could increase to 100 percent. There was a lot of discussion of why some women aren’t tested and if doctors can just try to assess whether there’s a risk that a family member might have the infection—even if those family members don’t know themselves that they’re infected.

Data and trust

Langer acknowledged there might be ways to assess risk from at least the mother in the 24-hour window after birth—”or,” he suggested, “you cannot have to worry about all of those different things that could go wrong, and you could simply give the vaccine because there is no data available that says that there is any harm that would come to a newborn compared to a one-month-old infant [getting the vaccine.]”

He summed up the discussion succinctly: “The only thing that we’re discussing here is if there’s some benefit or removal of harm that comes from waiting a month. And I have not seen any data that says that there is any benefit to the infant of waiting a month, but there are a number of potential harms to the infant of waiting a month.”

Panel member Robert Malone, who has falsely claimed that COVID-19 vaccines cause a form of AIDS, explained that the proposed change for the hep B vaccination was not due to any safety concern or evidence-based reason, but about trust among parents who have been exposed to vaccine misinformation.

“The signal that is prompting this is not one of safety, it is one of trust,” Malone said yesterday. “It is one of parents uncomfortable with this medical procedure being performed at birth in a rather unilateral fashion without significant informed consent at a time in particular when there has been a loss of trust in the public health enterprise and vaccines in general.”

Dashed decisions

But the questions and uncertainties of the proposed recommendation and the data behind it dogged the committee again this morning.

This morning, the voting language was put on a slide and immediately drew criticism. The language was:

If a mother tests [hepatitis B]-negative:

The first dose of the Hepatitis B vaccine is not given until the child is at least one month old.

Infants may receive a dose of Hepatitis B vaccine before one month according to individual based decision-making. *

*Also referred to as shared clinical decision-making.

Hibbeln, the psychiatrist, again pushed back, this time noting that the language of the change is confusing. “You can’t say don’t give it and then give an opportunity to give it,” he said, arguing that shared clinical decision-making is, essentially, all or nothing.

Discussion quickly spiraled, with another member questioning whether there was any data presented at all on the proposed recommendation. There was a fast motion to table the vote indefinitely, and the motion to table passed in a speedy vote of 11–1, with the ACIP chair, Martin Kulldorff, being the only holdout.

For the rest of the day, the panel is discussing COVID-19 vaccines. Stay tuned.

Beth is Ars Technica’s Senior Health Reporter. Beth has a Ph.D. in microbiology from the University of North Carolina at Chapel Hill and attended the Science Communication program at the University of California, Santa Cruz. She specializes in covering infectious diseases, public health, and microbes.

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In new level of stupid, RFK Jr.’s anti-vaccine advisors axe MMRV recommendation

ACIP, CDC, health, MMR, mmrv, robert f kennedy jr, vaccine / DJ Henderson / September 19, 2025

The vote to strip the recommendation came after a day of inept discussion.

An MMR and VAR vaccine ready for a pediatric vaccination at Kaiser Permanente East Medical offices in Denver in 2015. Credit: Getty | Joe Amon

The panel of vaccine advisors hand-selected by anti-vaccine activist Robert F. Kennedy Jr. voted on Thursday to change the federal vaccine recommendations for children, removing safe, well-established vaccine doses from current schedules and realizing Kennedy’s anti-vaccine agenda to erode federal vaccine policy and sow distrust.

Specifically, the panel—the Advisory Committee on Immunization Practices (ACIP)—voted to remove the Centers for Disease Control and Prevention’s previous recommendation for use of a measles, mumps, rubella, varicella (chickenpox) MMRV combination vaccine for children under 4 years old.

The context

In June, Kennedy fired all 17 highly qualified, highly vetted members of ACIP and quickly replaced them with seven questionable members, who largely did not have subject matter expertise. Moreover, many of them have clearly expressed anti-vaccine rhetoric and skepticism about pandemic responses and COVID-19 vaccines. At least two new members have been paid witnesses in trials against vaccine makers, a clear conflict of interest. Earlier this week, Kennedy added five additional members, who raise the same anti-vaccine concerns as the first group.

In the meeting today—the first of two all-day meetings—members made clear their inexperience and lack of expertise in evaluating vaccine policy. They asked basic questions about study data and analysis—such as asking what a “low confidence” designation means—and claimed CDC presentations lacked critical data when, in fact, a CDC scientist had just presented the exact data in question.

The first half of the day focused on the MMRV vaccine, while the second half focused on a newborn dose of the hepatitis B (hep B) vaccine. A vote was initially scheduled for that vaccine today, too, but was postponed after the panel decided to change the wording of the voting question. They meet again tomorrow to vote on the hep B recommendation as well as recommendations for this year’s COVID-19 vaccine. Ars Technica will have coverage of the second half of the meeting tomorrow, along with a report on the hepatitis B discussion today.

MMRV vaccine change

For the MMRV vaccine, the panel rehashed an issue that vaccine experts had thoroughly examined years ago. Currently, the CDC recommends children get vaccinated against measles, mumps, rubella, and varicella (chickenpox) twice—one dose at 12 to 15 months, and a second dose between the ages of 4 and 6 years.

In 2005, the Food and Drug Administration approved a combo shot for all four—the MMRV vaccine—which provided an alternative to the previous method of giving an MMR vaccine dose (against measles, mumps, and rubella) plus a separate varicella vaccine dose at the same time. (This vaccination strategy is shorthanded as MMR + V.) Thus, the MMRV combo shot meant one fewer shot for children. But, in 2008, post-market data suggested that the MMRV shot might have a slightly higher risk of causing febrile seizures (seizures associated with fevers), which is a very low risk with the MMR + V separate shots.

Febrile seizures are a somewhat common reaction in young children; this type of seizure almost entirely occurs in children under age 5 years, most often striking between 14 and 18 months. The seizures are short, usually less than a minute or two, and they can be caused by essentially anything that can cause a fever—ear infections, vaccines, the flu, etc. For parents, a febrile seizure can be very scary and lead them to bring their child to a doctor or hospital. However, febrile seizures are almost always harmless—the prognosis is “excellent,” as CDC staff experts noted. Nearly all children fully recover with no long-term problems. By age 5, up to 5 percent of all children have had a febrile seizure at some point, for some reason.

Low risks

In post-market studies of the MMRV vaccine, it was very clear that a slightly increased risk of febrile seizures was only linked to the first dose (given at 12 to 15 months, not the second, given at 4 to 6 years). In studies of over 400,000 children, data found that the risk of a febrile seizure after a first-dose MMRV vaccine was 7 to 8.5 seizure cases for every 10,000 vaccinations. That’s compared to 3.2 to 4.2 seizure cases in 10,000 vaccinations with MMR + V. In all, a first-dose MMRV vaccine had about one additional febrile seizure per 2,300 to 2,600 children vaccinated compared with MMR + V.

In 2009, CDC vaccine experts reviewed all the data and updated the vaccine recommendation. They maintained that MMRV and the MMR+V vaccinations are still both safe, effective, and recommended at both vaccination time points. But, they added the nuance that there is a preference (or a default, basically) for using the MMR + V shots for the first dose, unless a parent expressly wanted the MMRV vaccine for that first dose. This skirted the slightly increased risk of febrile seizure in young children, without entirely taking away the option if a parent prioritized fewer jabs and wanted the MMRV. For the second dose, again, both MMRV and MMR + V are options, but the CDC stated a preference for the one-shot MMRV.

Since then, about 85 percent of vaccinated children have gotten MMR + V for their first dose shots, with the other 15 percent getting the MMRV vaccine.

Inept discussion

In the discussion today, Kennedy’s members seemed to have little grasp of the issue at hand and the clinical significance of febrile seizures generally. They continued to circle back to unfounded concerns about febrile seizures and fringe theories about potential long-term effects.

Cody Meissner, a pediatric professor at Dartmouth’s Geisel School of Medicine who has served on ACIP in the past—arguably the most qualified of Kennedy’s new lineup—was bewildered at why the committee was rehashing the issue addressed years ago. “This discussion is really a déjà vu for me,” he said. Yet, while Meisner felt the issue was settled and pediatricians were well-equipped to calm parents’ fears about febrile seizures, the other members could not be swayed. They claimed, without evidence, that parents of children who have febrile seizures after a vaccine would be less likely to get future vaccines.

As the committee seemed to be leaning toward removing the recommendation for MMRV for the first dose, Jason Goldman, president of the American College of Physicians, who attended the meeting as a liaison, pushed back strongly. He pointed out that—as with the last time Kennedy’s ACIP met—they were not following the standard framework for making and changing recommendations.

“Are we going to have a thoroughly vetted evidence-to-recommend framework presentation that looks at all the harms benefits, acceptability, feasibility—with input from practicing clinicians and liaisons in order to make an informed decision?” Goldman asked. “I would argue that this recommendation is going to create more confusion among the public.”

Goldman noted that if the committee rescinds the recommendation for MMRV for children under 4, the shot would no longer be covered by the Vaccines for Children (VFC) Program, a federal program for Medicaid-eligible and under- or uninsured kids, which covers about half of American children.

“And finally, you are taking away the choice of parents to have informed consent and discussion with their physician on what they want to do for the health and benefit of their children,” Goldman said. “So, I urge this committee not to change the recommendations if they truly want to give the power to the parents to decide what is best for their child and allow them to make the choice in consultation with their physicians.”

Voting confusion

In the end, Kennedy’s panel voted 8–3 (with one abstention) to not recommend MMRV for children under age 4, meaning the MMRV vaccine could potentially no longer be available for some children under age 4. Private insurance companies are required to cover ACIP-recommended vaccines, so this move strips the recommendation and that coverage requirement.

But, anticipating such a change, AHIP, a trade organization representing insurance companies, put out a statement earlier this week suggesting that they would still cover the MMRV vaccine for children under 4, even if it’s not required.

“Health plans will continue to cover all ACIP-recommended immunizations that were recommended as of September 1, 2025, including updated formulations of the COVID-19 and influenza vaccines, with no cost-sharing for patients through the end of 2026,” the statement reads.

But, there’s more: In a second vote today, ACIP voted 8–1 (with three abstentions) against changing VFC coverage for MMRV. Therefore, the VFC program will continue to cover MMRV vaccines for children under age 4. This is a split from standard policy that is likely to spur confusion, because VFC typically goes with ACIP recommendations. Also, Medicaid’s Children’s Health Insurance Program (CHIP) has to follow the ACIP vaccine recommendation and thus will no longer cover MMRV for children under age 4 covered by CHIP.

One of the abstentions on the VFC coverage vote was Meissner, who didn’t want to strip the recommendation or the VFC coverage but was entirely confused by how this would work in practice.

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RFK Jr. adds more anti-vaccine members to CDC vaccine advisory panel

ACIP, anti-vaccine, CDC, COVID-19 vaccines, health, hepatitis B, measles, robert f kennedy jr / Mike M. / September 16, 2025

Kirk Milhoan, a pediatric cardiologist who is a senior fellow at the Independent Medical Alliance (formerly Front Line COVID-19 Critical Care Alliance), which promotes misinformation about COVID-19 vaccines and touts unproven and dubious COVID-19 treatments. Those include the malaria drug hydroxychloroquine, the de-worming drug ivermectin, and various concoctions of vitamins and other drugs. Milhoan has stated that mRNA COVID-19 vaccines should be removed from the market, telling KFF in March: “We should stop it and test it more before we move forward.”

Evelyn Griffin, an obstetrician and gynecologist in Louisiana who reportedly lost her job for refusing to get a COVID-19 vaccine. In a speech at a Louisiana Health Freedom Day in May 2024, Griffin claimed that doctors “blindly believed” that mRNA COVID-19 vaccines were safe. She has also claimed that the vaccines cause “bizarre and rare conditions,” according to the Post.

Hillary Blackburn, a pharmacist in St. Louis. Reuters reports that she is the daughter-in-law of Sen. Marsha Blackburn (R-Tenn.), who has opposed vaccine mandates.

Raymond Pollak, a semi-retired transplant surgeon who filed a whistleblower lawsuit against the University of Illinois Hospital in 1999, alleging the hospital manipulated patient data to increase their chances of receiving livers. The hospital settled the suit, paying $2.5 million, while denying wrongdoing.

ACIP is scheduled to meet at the end of this week, on September 18 and September 19. According to an agenda recently posted online, the committee will vote on recommendations for a measles, mumps, rubella, and varicella (MMRV) combination vaccine, the Hepatitis B vaccine, and this year’s updated COVID-19 vaccines. Vaccine experts widely fear that the committee will rescind recommendations and restrict access to those vaccines. Such moves will likely create new, potentially insurmountable barriers for people, including children, to get vaccines.

ACIP-recommended vaccines are required to be covered by private health insurance plans and the Vaccines for Children program for Medicaid-eligible and under- or uninsured kids, which covers about half of American children. Without ACIP recommendations for a vaccine, insurance coverage would be an open question, and vulnerable children would simply lose access entirely.

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RFK Jr.’s CDC may limit COVID shots to 75 and up, claim they killed kids

CDC, COVID-19, fda, health, kennedy, mRNA, vaccines / Shannon Garcia / September 13, 2025

While some experts and health care providers had hoped that next week’s ACIP meeting would add clarity to the situation and allow healthy adults and children better access to the shots, the Post’s reporting suggests that’s unlikely. According to their sources, Kennedy’s ACIP is considering recommending the vaccines to those 75 and older, while instructing those 74 and younger to speak with their doctor about getting a shot. Another reported option is to not recommend the vaccine to people under the age of 75 at all, unless they have a preexisting condition.

Backlash

Such additional restrictions would likely intensify the backlash against Kennedy’s anti-vaccine agenda. Already, medical organizations have taken the unprecedented action to release their own evidence-based guidances that maintain COVID-19 vaccine recommendations for healthy children, particularly those under age 2, pregnant people, and healthy adults. Many medical and health organizations, as well as lawmakers, and over 1,000 current and former HHS employees have also called for Kennedy to resign.

Criticism of Kennedy’s actions has spread across party lines. Sen. Bill Cassidy (R-La.), a vaccine-supporting physician who cast a critical vote for Kennedy’s confirmation, had accused Kennedy of denying people vaccines and called for next week’s ACIP meeting to be postponed.

“Serious allegations have been made about the meeting agenda, membership, and lack of scientific process being followed for the now announced September ACIP meeting,” Cassidy said. “These decisions directly impact children’s health, and the meeting should not occur until significant oversight has been conducted. If the meeting proceeds, any recommendations made should be rejected as lacking legitimacy given the seriousness of the allegations and the current turmoil in CDC leadership.”

Meanwhile, in a clear rebuff of Kennedy’s cancellation of mRNA vaccine funding, the Republican-led House Committee on Appropriations this week passed a 2026 spending bill that was specifically amended to inject the words “including of mRNA vaccines” into a sentence about pandemic preparedness funding. The bill now reads: “$1,100,000,000, to remain available through September 30, 2027, shall be for expenses necessary to support advanced research and development, including of mRNA vaccines, pursuant to section 319L of the PHS Act and other administrative expenses of the Biomedical Advanced Research and Development Authority.”

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Child dies of horrifying measles complication in Los Angeles

CDC, child, death, health, Infectious disease, Los Angeles, measles, sspe, vaccine / Beth Washington / September 12, 2025

A child in Los Angeles has died of a measles-related brain disorder stemming from an infection in infancy, the Los Angeles County health department reported Thursday.

Specifically, the child died of subacute sclerosing panencephalitis (SSPE), a rare but always fatal complication that strikes years after an initial measles infection. The health department’s announcement offered few details about the child, including the child’s age, but said that the child had contracted the virus before they were old enough to be vaccinated against measles. The first of two recommended doses of measles, mumps, and rubella (MMR) vaccine is given between 12 and 15 months.

“This case is a painful reminder of how dangerous measles can be, especially for our most vulnerable community members,” Muntu Davis, a Los Angeles County health officer, said in a statement. “Infants too young to be vaccinated rely on all of us to help protect them through community immunity. Vaccination is not just about protecting yourself—it’s about protecting your family, your neighbors, and especially children who are too young to be vaccinated.”

SSPE is caused by a persistent measles infection in the central nervous system. Children infected with the virus may go through the standard disease progression—flu-like symptoms, high fever, the telltale rash—and then appear to fully recover. But, for a small few, the virus remains, and SSPE emerges years later, often seven to 10 years after the initial infection.

The Los Angeles health department noted that SSPE generally affects about 1 in 10,000 people with measles, but the risk may be much higher—about 1 in 600—for those who get measles as infants, such as the child who recently died.

With widespread vaccination, which led to measles being declared eliminated from the US in 2000, SSPE has virtually disappeared in the US. However, with vaccination rates slipping and anti-vaccine misinformation and views gripping the country, health experts fear seeing more of these devastating cases. Already, the US measles case count for the year is at a 33-year high, and two other children, as well as an adult, died from the acute infection this year.

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Ousted CDC director to testify before Senate after RFK Jr. called her a liar

ACIP, CDC, COVID-19, health, robert f kennedy jr, Senate, vaccines / 9u50fv / September 11, 2025

Kennedy is reportedly vetting seven additional members for ACIP, who may be added before the next meeting. They include additional anti-vaccine voices and fringe members of the medical community, such as Kirk Milhoan, who promoted the de-worming drug ivermectin to treat COVID-19, despite several clinical trials finding it is not effective. There is also Joseph Fraiman, who has repeatedly called for COVID-19 vaccines to be pulled from the market.

Also on the list is Catherine Stein, who, The Washington Post noted, has advocated against vaccine mandates and wrote a 2021 article arguing that people should not be afraid of contracting COVID-19 because: “Our Lord has given us a mission to share the gospel. If we live in fear of death, that weakens our testimony. Remember, the Lord Jesus did not fear lepers, and leprosy was (and continues to be) a highly contagious infectious disease.”

Leprosy, or Hansen’s disease, is, in fact, not a highly contagious disease. It does not spread easily from person to person, is not spread through casual contact, and about 95 percent of people are immune to it naturally. COVID-19, meanwhile, is estimated to have caused more than 7 million deaths worldwide since the start of the pandemic.

Regardless of whether these candidates are added to the roster, Cassidy has called for the ACIP meeting scheduled for September 18 and 19 to be postponed.

“Serious allegations have been made about the meeting agenda, membership, and lack of scientific process being followed for the now announced September ACIP meeting,” Cassidy said. “These decisions directly impact children’s health and the meeting should not occur until significant oversight has been conducted. If the meeting proceeds, any recommendations made should be rejected as lacking legitimacy given the seriousness of the allegations and the current turmoil in CDC leadership.”

After Monarez and Houry testify before the HELP committee, Cassidy said that Senators are planning to invite current health officials to respond in a subsequent hearing.

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Who can get a COVID vaccine—and how? It’s complicated.

ACIP, CDC, COVID-19, fda, health, mRNA, pharmacists, robert f kennedy jr, vaccines / Mike M. / September 6, 2025

We’re working with a patchwork system, and there are a lot of gray areas.

Vaccinations were available at CVS in Huntington Park, California, on August 28, 2024. Credit: Getty | Christina House

As fall approaches and COVID cases tick up, you might be thinking about getting this season’s COVID-19 vaccine. The annually updated shots have previously been easily accessible to anyone over 6 months of age. Most people could get them at no cost by simply walking into their neighborhood pharmacy—and that’s what most people did.

However, the situation is much different this year with an ardent anti-vaccine activist, Robert F. Kennedy Jr., as the country’s top health official. Since taking the role, Kennedy has worked diligently to dismantle the country’s premier vaccination infrastructure, as well as directly hinder access to lifesaving shots. That includes restricting access to COVID-19 vaccines—something he’s done by brazenly flouting all standard federal processes while providing no evidence-based reasoning for the changes.

How we got here

In late May, Kennedy unilaterally decided that all healthy children and pregnant people should no longer have access to the shots. He announced the unprecedented change not through official federal channels, but via a video posted on Elon Musk’s X platform. Top vaccine and infectious disease officials at the Centers for Disease Control and Prevention—which sets federal vaccination recommendations—said they also learned of the change via X.

Medical experts—particularly the American Academy of Pediatrics (AAP) and the American College of Obstetricians and Gynecologists (ACOG)—immediately slammed the change, noting that data continues to indicate pregnant women and children under age 2 are particularly vulnerable to severe COVID-19. Both medical groups have since released their own vaccination guidance documents that uphold COVID-19 vaccine recommendations for those patient groups. (AAP here, ACOG here)

Nevertheless, in line with Kennedy, officials at the Food and Drug Administration signaled that they would take the unprecedented, unilateral step of changing the labels on the vaccines to limit who could get them—in this case, people 65 and over, and children and adults with health conditions that put them at risk of severe COVID-19. Kennedy’s FDA underlings—FDA Commissioner Martin Makary and top vaccine regulator, Vinay Prasad—laid out the plans alongside a lengthy list of health conditions in a commentary piece published in the New England Journal of Medicine. The list includes pregnancy—which is evidence-based, but odd, since it conflicts with Kennedy.

What was supposed to happen

When there isn’t a zealous anti-vaccine activist personally directing federal vaccine policy, US health agencies have a thorough, transparent protocol for approving and recommending vaccinations. Generally, it starts with the FDA, which has both its own scientists and a panel of outside expert advisors to review safety and efficacy data submitted by a vaccine’s maker. The FDA’s advisory committee—the Vaccines and Related Biological Products Advisory Committee (VRBPAC)—then holds a completely public meeting to review, analyze, and discuss the data. They make a recommendation on a potential approval and then the FDA commissioner can decide to sign off, typically in accordance with internal experts.

Resulting FDA approvals or authorizations are usually broad, basically covering people who could safely get the vaccine. The specifics of who should get the vaccine fall to the CDC.

Once the FDA approves or authorizes a vaccine, the CDC has a similar evaluation process. Internal experts review all the data for the vaccine, plus the epidemiological and public health data to assess things like disease burden, populations at risk, resource access, etc. A committee of outsides expert advisors do the same—again in a totally transparent public meeting that is livestreamed with all documents and presentations available on the CDC’s website.

That committee, the Advisory Committee on Immunization Practices (ACIP), then makes recommendations to the CDC about how the shots should be used. These recommendations can provide nuanced clinical guidance on exactly who should receive a vaccine, when, in what scenarios, and in what time series, etc. The recommendations may also be firm or soft—e.g., some people should get a vaccine, while others may get the vaccine.

The CDC director then decides whether to adopt ACIP’s recommendations (the director usually does) and updates the federal immunization schedules accordingly. Those schedules set clinical standards for immunizations, including routine childhood vaccinations, nationwide. Once a vaccine recommendation makes it to the ACIP-guided federal immunization schedules, private health insurance companies are required to cover those recommended vaccinations at no cost to members. And—a key catch for this year—19 states tie ACIP vaccine recommendations to pharmacists’ ability to independently administer vaccines.

What actually happened

Days after Kennedy’s X announcement of COVID-19 vaccine restrictions in late May, the CDC changed the federal immunization schedules. The recommendation for a COVID-19 shot during pregnancy was removed. But, for healthy children 6 months to 17 years, the CDC diverged from Kennedy slightly. The updated schedule doesn’t revoke access outright; instead, it now says that healthy children can get the shots if there is shared decision-making with the child’s doctor, that is, if the parent/child wants to get the vaccine and the doctor approves. ACIP was not involved in any of these changes.

On August 27, the FDA followed through with its plans to change the labels on COVID-19 vaccines, limiting access to people who are 65 and older and people who have an underlying condition that puts them at high risk of severe COVID-19.

FDA’s advisory committee, VRBPAC, met in late May, just a few days after FDA officials announced their plans to restrict COVID-19 vaccine access. The committee was not allowed to discuss the proposed changes. Instead, it was limited to discussing the SARS-CoV-2 strain selection for the season, and questions about the changes were called “off topic” by an FDA official.

ACIP, meanwhile, has not met to discuss the use of the updated COVID-19 vaccines for the 2025–2026 season. Last year, ACIP met and set the 2024–2025 COVID-19 shot recommendations in June. But, instead, in June of this year, Kennedy fired all 17 members of ACIP, falsely claiming members were rife with conflicts of interest. He quickly repopulated ACIP with anti-vaccine allies who are largely unqualified and some of whom have been paid witnesses in lawsuits against vaccine makers, a clear conflict of interest. While Kennedy is reportedly working to pack more anti-vaccine activists onto ACIP, the committee is scheduled to meet and discuss the COVID-19 vaccine on September 18 and 19. The committee will also discuss other vaccines.

Outside medical and public health experts view ACIP as critically compromised and expect it will further restrict access to vaccines.

With this set of events, COVID-19 vaccine access is in disarray. Here’s what we do and don’t know about access.

Getting a vaccine

FDA vaccine criteria

Prior to Kennedy, COVID-19 vaccines were available to all people ages 6 months and up. But that is no longer the case. The current FDA approvals are as follows:

Pfizer’s mRNA COVID-19 vaccine (COMIRNATY) is only available to people:

65 years of age and older, or
5 years through 64 years of age with at least one underlying condition that puts them at high risk for severe outcomes from COVID-19.

Moderna’s mRNA COVID-10 vaccine (SPIKEVAX) is only available to people:

65 years of age and older, or
6 months through 64 years of age with at least one underlying condition that puts them at high risk for severe outcomes from COVID-19.

Novavax’s protein subunit COVID-19 vaccine NUVAXOVID is only available to people:

65 years of age and older, or
12 years through 64 years of age with at least one underlying condition that puts them at high risk for severe outcomes from COVID-19.

Who can get a COVID-19 vaccine and where now depends on a person’s age, underlying conditions, and the state they reside in.

States-based restrictions

The fact that ACIP has not set recommendations for the use of 2025–2026 COVID-19 vaccines means vaccine access is a messy patchwork across the country. As mentioned above, 19 states link pharmacists’ ability to independently provide COVID-19 vaccines to ACIP recommendations. Without those recommendations, pharmacies in those states may not be able to administer the vaccines at all, or only provide them with a doctor’s prescription—even for people who fit into the FDA’s criteria.

Last week, The New York Times reported that CVS and Walgreens, the country’s largest pharmacy chains, were either not providing vaccines or requiring prescriptions in 16 states. And the list of 16 states where CVS had those restrictions was slightly different than where Walgreens had them, likely due to ambiguities in state-specific regulations.

The National Alliance of State Pharmacy Associations (NASPA) and the American Pharmacists Association (APhA) have a state-by-state overview of pharmacist vaccination authority regulations here.

For people meeting the FDA criteria

In the 31 states that allow for broader pharmacist vaccination authority, people meeting FDA’s criteria (65 years and older, and people with underlying conditions), should be able to get the vaccine at a pharmacy like usual. And once ACIP sets recommendations later this month—assuming the committee doesn’t restrict access further—people in those groups should be able to get them at pharmacies in the remaining states, too.

Proving underlying conditions

People under 65 with underlying health conditions who want to get their COVID-19 shot at a pharmacy will likely have to do something to confirm their eligibility.

Brigid Groves, APhA’s vice president of professional affairs and the organization’s expert on vaccine policy, told Ars that the most likely scenario is that people will have to fill out forms prior to vaccination, indicating the conditions they have that make them eligible, a process known as self-attestation. This is not unusual, Groves noted. Other vaccinations require such self-attestation of conditions, and for years, this has been sufficient for pharmacists to administer vaccines and for insurance policies to cover those vaccinations, she said.

“APhA is a strong supporter of that patient self-attestation, recognizing that patients have a very good grasp of their medical conditions,” Groves said.

For people who don’t meet the FDA criteria

There are a lot of reasons why healthy children and adults outside the FDA’s criteria may still want to get vaccinated: Maybe they are under the age of 2, an age that is, in fact, still at high risk of severe COVID-19; maybe they live or work with vulnerable people, such as cancer patients, the elderly, or immunocompromised; or maybe they just want to avoid a crummy respiratory illness that they could potentially pass on to someone else.

For these people, regardless of what state they are in, getting the vaccine would mean a pharmacist or doctor would have to go “off-label” to provide it.

“It’s very gray on how a pharmacist may proceed in that scenario,” Groves told Ars. Going off-label could open pharmacists up to liability concerns, she said. And even if a patient can obtain a prescription for an off-label vaccine, that still may not be enough to allow a pharmacist to administer the vaccine.

“Pharmacists have something called ‘corresponding responsibility,’ Groves explained. “So even if a physician, or a nurse practitioner, or whomever may send a prescription over for that vaccine, that pharmacist still has that responsibility to ensure this is the right medication, for the right patient, at the right time, and that they’re indicated for it,” she said. So, it would still be going outside what they’re technically authorized to do.

Doctors, on the other hand, can administer vaccines off-label, which they might do if they choose to follow guidance from medical organizations like AAP and ACOG, or if they think it’s best for their patient. They can do this without any heightened professional liability, contrary to some suggestions Kennedy has made (doctors prescribe things off-label all the time). But, people may have to schedule an appointment with their doctor and convince them to provide the shot—a situation far less convenient than strolling into a local pharmacy. Also, since pharmacies have provided the vast majority of COVID-19 vaccines so far, some doctors’ offices may not have them on hand.

Pregnancy

It’s unclear if pregnancy still falls under the FDA’s criteria for a high-risk condition. It was included in the list that FDA officials published in May. However, the agency did not make that list official when it changed the vaccine labels last month. Some experts have suggested that, in this case, the qualifying high-risk conditions default to the CDC’s existing list of high-risk conditions, which includes pregnancy. But it’s not entirely clear.

In addition, with Kennedy’s previous unilateral change to the CDC’s immunization schedule—which dropped the COVID-19 vaccine recommendation during pregnancy—pregnant people could still face barriers to getting the vaccine in the 19 states that link pharmacist authorization to ACIP recommendations. That could change if ACIP reverses Kennedy’s restriction when the committee meets later this month, but that may be unlikely.

Insurance coverage

It’s expected that insurance companies will continue to cover the full costs of COVID-19 vaccines for people who meet the FDA criteria. For off-label use, it remains unclear.

Groves noted that in June, AHIP, the trade organization for health insurance providers, put out a statement suggesting that it would continue to cover vaccines at previous levels.

“We are committed to ongoing coverage of vaccines to ensure access and affordability for this respiratory virus season. We encourage all Americans to talk to their health care provider about vaccines,” the statement reads.

However, Groves was cautious about how to interpret that. “At the end of the day, on the claims side, we’ll see how that pans out,” she said.

Rapidly evolving access

While the outcome of the ACIP meeting on September 18 and 19 could alter things, a potentially bigger source of change could be actions by states. Already, there have been rapid responses with states changing their policies to ensure pharmacists can provide vaccines, and states making alliances with other states to provide vaccine recommendations and vaccines themselves.

Who can get a COVID vaccine—and how? It’s complicated. Read More »

RFK Jr. says COVID shots still available to all as cancer patients denied access

CDC, COVID-19 vaccine, health, kennedy, robert f kennedy jr, Senate / Shannon Garcia / September 5, 2025

Here are some key moments from today’s hearing:

Untrustworthy

With the fallout ongoing from the abrupt ouster of CDC Director Susan Monarez last week, many senators focused on what led to her downfall. In a Wall Street Journal op-ed published two hours before the hearing, Monarez confirmed media reports that she had been fired by Kennedy for refusing to rubber-stamp changes to CDC vaccine guidance based on recommendations from Kennedy’s hand-selected advisors.

“I was told to preapprove the recommendations of a vaccine advisory panel newly filled with people who have publicly expressed antivaccine rhetoric,” Monarez wrote in the op-ed. She said she refused, insisting that the panel’s recommendations be “rigorously and scientifically reviewed before being accepted or rejected.”

In today’s hearing, Senators directly confronted Kennedy with that statement from the op-ed. Kennedy repeatedly said that she is lying and that he never directed her to preapprove vaccine recommendations. Instead, he claims, he told her to resign after he asked her directly if she was a trustworthy person, and she replied, ‘No.”

After several exchanges about this with other senators, Bernie Sanders (I-Vt.) picked it apart further, saying:

“Are you telling us that the former head of CDC went to you, you asked her, ‘Are you a trustworthy person?’ And she said, ‘No, I am not a trustworthy person,'” Sanders asked.

“She didn’t say ‘No, I’m not a trustworthy person,'” Kennedy replied. “She said, ‘No.’ I’m giving a quote.”

After that, Sen. Thom Tillis (R-NC), who seemed skeptical of Kennedy’s arguments generally, pointed out the absurdity of the claim, quoting Kennedy’s previous praise of Monarez. “I don’t see how you go—over four weeks—from a public health expert with ‘unimpeachable scientific credentials,’ a longtime champion of MAHA values, caring and compassionate and brilliant microbiologists, and four weeks later fire her,” Tillis said. “As somebody who advised executives on hiring strategies, number one, I would suggest in the interview you ask ’em if they’re truthful rather than four weeks after we took the time of the US Senate to confirm the person.”

RFK Jr. says COVID shots still available to all as cancer patients denied access Read More »

CDC spiraled into chaos this week. Here’s where things stand.

CDC, health, rfk jr / 9u50fv / August 30, 2025

CDC is in crisis amid an ouster, resignations, defiance, and outraged lawmakers.

Demetre Daskalakis, former director of the National Center for Immunization and Respiratory Diseases at the Centers for Disease Control and Prevention (CDC), center, embraces a supporter during a clap out outside of the Centers for Disease Control and Prevention (CDC) headquarters in Atlanta, Georgia, US, on Thursday, Aug. 28, 2025. Credit: Getty | Dustin Chambers

The US Centers for Disease Control and Prevention descended into turmoil this week after Health Secretary and zealous anti-vaccine advocate Robert F. Kennedy Jr. ousted the agency’s director, Susan Monarez, who had just weeks ago been confirmed by the Senate and earned Kennedy’s praise for her “unimpeachable scientific credentials.”

It appears those scientific chops are what led to her swift downfall. Since the Department of Health and Human Services announced on X late Wednesday that “Susan Monarez is no longer director” of the CDC, media reports have revealed that her forced removal was over her refusal to bend to Kennedy’s anti-vaccine, anti-science agenda.

The ouster appeared to be a breaking point for the agency overall, which has never fully recovered from the public pummeling it received at the height of the COVID-19 pandemic. In its weakened position, the agency has since endured an onslaught of further criticism, vilification, and misinformation from Kennedy and the Trump administration, which also delivered brutal cuts, significantly slashing CDC’s workforce, shuttering vital health programs, and hamstringing others. Earlier this month, a gunman, warped by vaccine misinformation, opened fire on the CDC’s campus, riddling its buildings with hundreds of bullets, killing a local police officer, and traumatizing agency staff.

Monarez’s expulsion represents the loss of a scientifically qualified leader who could have tried to shield the agency from some ideological attacks. As such, it quickly triggered a cascade of high-profile resignations at the CDC, a mass walkout of its staff, and outrage among lawmakers and health experts. While the fallout of the ouster is ongoing, what is immediately clear is that Kennedy is relentlessly advancing his war against lifesaving vaccines from within the CDC and is forcing his ideological agenda on CDC experts.

Some of those very CDC experts now warn that the CDC can no longer be trusted and the country is less safe.

Here’s what we know so far about the CDC’s downturn:

The ouster

Late Wednesday, The Washington Post reported that, for days prior to her ouster, Monarez had stood firm against Kennedy’s demands that she, and by extension the CDC, blindly support and adopt vaccine restrictions put forward by the agency’s vaccine advisory panel—a panel that Kennedy has utterly compromised. After firing all of its highly qualified, extensively vetted members in June, Kennedy hastily installed hand-selected allies on the Advisory Committee on Immunization Practices (ACIP), who are painfully unqualified but share Kennedy’s hostility toward lifesaving shots. Already, Kennedy’s panel has made recommendations that contradict scientific evidence and public health.

It is widely expected that they will further undo the agency’s evidence-based vaccine recommendations, particularly for COVID-19 and childhood shots. Experts fear that such changes would undermine public confidence in both vaccines and federal guidance, and make vaccines more difficult, if not impossible, for Americans to obtain. Kennedy has already restricted access to COVID-19 vaccines, prompting medical associations to produce divergent recommendations, which raises a slew of unanswered questions about access to the vaccines.

Amid the standoff over rolling back vaccine policy, Kennedy urged Monarez to resign. She refused, and instead called key senators for help, including Bill Cassidy (R-La.), who cast a critical vote in favor of Kennedy’s confirmation in exchange for concessions that Kennedy would not upend CDC’s vaccine recommendations.

Cassidy then called Kennedy, which angered the anti-vaccine advocate, who then chastised Monarez. The beleaguered director was then presented with the choice to resign or be fired. She continued to refuse to resign. On Wednesday evening, HHS wrote of her termination on X. But Monarez, speaking through her lawyers, reiterated that she would not resign and had not been notified of her termination. Late Wednesday night, her lawyers confirmed that White House officials had sent notification of termination, but she still refused to vacate the role.

“As a presidential appointee, senate confirmed officer, only the president himself can fire her,” her lawyers, Mark Zaid and Abbe Lowell said in a statement emailed to Ars Technica. “For this reason, we reject the notification Dr. Monarez has received as legally deficient and she remains as CDC Director. We have notified the White House Counsel of our position.”

On Thursday, the Post reported that the White House had already named a replacement. Jim O’Neill, currently the deputy secretary of HHS, is to be the interim leader of the CDC. O’Neill was previously a Silicon Valley investor and entrepreneur who became a close ally of Peter Thiel. He also worked as a federal official in the George W. Bush administration. During the COVID-19 pandemic, he was a frequent critic of the CDC, but at his Senate confirmation hearing in May, he called himself “very strongly pro-vaccine.”

Kennedy, meanwhile, went on Fox News’ Fox and Friends program Thursday and said the CDC is “in trouble” and that “we’re fixing it. And it may be that some people should not be working there anymore.”

Kennedy’s ACIP is now scheduled to meet September 18–19 to discuss COVID-19 shots, among other vaccines.

Response at the CDC

Soon after news broke of Monarez’s removal, three high-ranking CDC officials resigned together: Daniel Jernigan, director of the National Center for Emerging Zoonotic Infectious Diseases; Debra Houry, chief medical officer; and Demetre Daskalakis, director of the National Center for Immunization and Respiratory Diseases.

Their resignation letters spoke to the dangers of Kennedy’s anti-vaccine, anti-science agenda.

“For the good of the nation and the world, the science at CDC should never be censored or subject to political pauses or interpretations,” Houry wrote in her resignation letter. “Vaccines save lives—this is an indisputable, well-established, scientific fact. … It is, of course, important to question, analyze, and review research and surveillance, but this must be done by experts with the right skills and experience, without bias, and considering the full weight of scientific evidence. Recently, the overstating of risks and the rise of misinformation have cost lives, as demonstrated by the highest number of US measles cases in 30 years and the violent attack on our agency.”

In his resignation letter, Daskalakis slammed Kennedy for his lack of transparency, communication, and interest in evidence-based policy. He accused the anti-vaccine advocate of using the CDC as “a tool to generate policies and materials that do not reflect scientific reality and are designed to hurt rather than to improve the public’s health.” He also blasted ACIP’s COVID work group members as having “dubious intent and more dubious scientific rigor.”

“The intentional eroding of trust in low-risk vaccines favoring natural infection and unproven remedies will bring us to a pre-vaccine era where only the strong will survive and many if not all will suffer,” Daskalakis wrote. “I believe in nutrition and exercise. I believe in making our food supply healthier, and I also believe in using vaccines to prevent death and disability. Eugenics plays prominently in the rhetoric being generated and is derivative of a legacy that good medicine and science should continue to shun.”

In a conversation with The New York Times published Friday, Daskalakis revealed that Kennedy has never accepted a briefing from his center’s experts and said the resignations should indicate that “there’s something extremely wrong [at CDC].

“And also I think it’s important for the American public to know that they really need to be cautious about the recommendations that they’re hearing coming out of ACIP,” he added.

As the three leaders were escorted out of the CDC on Thursday, the staff held a boisterous rally to show support for them and their agency. On his way out, Jernigan, who worked at CDC for more than 30 years, praised his colleagues.

“What makes us great at CDC is following the science, so let’s get the politics out of public health,” he said to cheers. “Let’s get back to the objectivity and let the science lead us, because that’s how we get to the best decisions for public health.”

While those three resignations made news on Wednesday and Thursday, they are part of a steady stream of exits from the agency since Kennedy became secretary. Earlier on Wednesday, Politico reported that Jennifer Layden, director of the agency’s Office of Public Health Data, Surveillance, and Technology, had also resigned.

Response outside the CDC

Lawmakers have expressed concern and even outrage over Monarez’s firing and what’s going on at the CDC.

Sen. Bernie Sanders (I-Vt.) quickly demanded a bipartisan investigation into Monarez’s firing, calling Kennedy’s actions “reckless” and “dangerous.”

He went on to blast Kennedy’s work as health secretary. “In just six months, Secretary Kennedy has completely upended the process for reviewing and recommending vaccines for the public,” Sanders said. “He has unilaterally narrowed eligibility for COVID vaccines approved by the FDA, despite an ongoing surge in cases. He has spread misinformation about the safety and effectiveness of vaccines during the largest measles outbreak in over 30 years. He continues to spread misinformation about COVID vaccines. Now he is pushing out scientific leaders who refuse to act as a rubber stamp for his dangerous conspiracy theories and manipulate science.”

Sanders called on Cassidy, chair of the Senate Health, Education, Labor, and Pensions (HELP) Committee, to immediately convene a public hearing with Kennedy and Monarez.

Cassidy called for the upcoming ACIP meeting to be postponed.

“Serious allegations have been made about the meeting agenda, membership, and lack of scientific process being followed for the now announced September ACIP meeting,” Cassidy said in a statement. “These decisions directly impact children’s health and the meeting should not occur until significant oversight has been conducted. If the meeting proceeds, any recommendations made should be rejected as lacking legitimacy given the seriousness of the allegations and the current turmoil in CDC leadership.”

Outside health organizations also expressed alarm about the situation at the CDC.

The American Medical Association said it was “deeply troubled” by the agency’s turmoil and called Monarez’s ouster and the other resignations “highly alarming at a challenging moment for public health.”

In a joint press conference on Thursday of the Infectious Disease Society of America and the American Public Health Association, leaders for the groups spoke of the ripple effects in the public health community and the American public more broadly.

“When leadership decisions weaken the CDC, every American becomes more vulnerable to outbreaks, pandemics, and bioterror threats,” Wendy Armstrong, vice president of the Infectious Disease Society of America said in the briefing. “We’re speaking out because protecting public health is our responsibility as physicians and scientists. It’s imperative that the White House and Congress take action to ensure a functioning CDC as the current HHS Secretary Robert Kennedy has failed.”

Georges Benjamin, executive director of the American Public Health Association, echoed the call, saying, “We’ve had enough.”

CDC spiraled into chaos this week. Here’s where things stand. Read More »

CDC director has been ousted just weeks after Senate confirmation

CDC, health, Monarez, robert f kennedy jr / Beth Washington / August 28, 2025

Georges Benjamin, executive director of the American Public Health Association, told the outlet that Monarez “values science, is a solid researcher, and has a history of being a good manager. We’re looking forward to working with her.”

A low point for the agency

The reported ouster comes at what feels like a nadir for the CDC. The agency has lost hundreds of staff from layoffs and buyouts. Vital health programs have been shuttered or hampered. Dangerous rhetoric and health misinformation from Kennedy and other health officials in the Trump administration have made once-respected CDC experts feel vilified by the public and like targets of hate. Kennedy himself has falsely called the COVID-19 shots the “deadliest vaccine ever made” and the CDC a “cesspool of corruption,” for example.

On August 8, a gunman warped by vaccine disinformation opened fire on the CDC campus. Of nearly 500 shots fired, about 200 struck six CDC buildings as terrified staff dove for safety. One local police officer was killed in the incident. The gunman had specifically targeted the CDC for the shooting and blamed COVID-19 vaccines for his health problems.

Additional exits reported

After news broke of Monarez’s removal, Stat News reported that a wave of CDC leadership has resigned. The high-ranking resignations include: Daniel Jernigan, director of the National Center for Emerging Zoonotic Infectious Diseases; Deb Houry, Chief Medical Officer; and Demetre Daskalakis, director of the National Center for Immunization and Respiratory Diseases.

“I am not able to serve in this role any longer because of the ongoing weaponization of public health,” Daskalakis said in a message to staff seen by Stat.

“I am committed to protecting the public’s health, but the ongoing changes prevent me from continuing in my job as a leader of the agency,” Houry wrote in a message to staff. Houry added that science should “never be censored or subject to political interpretations.”

Earlier today, Politico reported that Jennifer Layden, director of the agency’s Office of Public Health Data, Surveillance, and Technology, has also resigned.

8/27/2025 8: 15 pm ET: This post has been updated to include the social media post from HHS, reporting from the Washington Post on the circumstances around Monarez’s exit, additional resignations reported by Stat and Politico, and the statement from Monarez’s lawyers.

CDC director has been ousted just weeks after Senate confirmation Read More »