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CDC Panel Votes to Nix Current Covid Vaccine Recommendations
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CDC Panel Votes to Nix Current Covid Vaccine Recommendations

by admin September 20, 2025


On Friday, the Advisory Committee on Immunization Practices (ACIP) voted to drop its recommendation that U.S. adults should generally receive the covid-19 vaccine, instead endorsing an individualized approach.

In a unanimous decision, the ACIP members agreed that adults 65 and older should decide on their own or with their doctor whether to get vaccinated for covid-19. The ACIP also recommended that people between the ages of 6 months and 64 years make an individual decision about covid-19 vaccination (yes, you read that correctly), while being informed that the benefits of vaccination are most apparent in those at higher risk of severe illness.

A screencap of ACIP blurbage articulating the new recommendations. © ACIP

The ACIP narrowly avoided recommending that Americans should require a prescription to get the covid-19 shot, however, though only barely.

A chaotic ACIP meeting

The votes capped off a chaotic and disorganized discussion held Friday over the safety and effectiveness of the covid-19 mRNA vaccines.

Retsef Levi, a longtime skeptic of the covid-19 vaccines and a professor of operations management at MIT Sloan School of Management, led the ACIP discussion, as well as the working group on covid-19 vaccines. Levi is one of several ACIP members handpicked by Health Secretary Robert Kennedy Jr. who has a long history of misrepresenting vaccine research.

CDC staff presented reams of evidence that covid-19 vaccines, even today, still reliably prevent serious outcomes like hospitalization and death, including in very young children. Many outside experts also testified in support of maintaining widespread access to these vaccines for every American who wants them. But ACIP members often questioned the findings or made their own poorly evidenced attempts to attack the safety of the vaccines.

At one point, for instance, ACIP members argued in support of a paper claiming to show extensive DNA contamination of the vaccines—a study that outside experts have criticized for glaring flaws and that is now being reviewed over potential concerns by its publisher. At another point, members argued that the covid-19 vaccines could possibly raise the risk of cancer, a claim widely refuted by most experts (mRNA vaccine technology is actively being studied as a way to prevent and treat certain cancers).

What this vote means for covid vaccine access

The language of the ACIP votes today was not disclosed until the very last minute, and it’s not entirely clear how they will impact vaccine access.

Late last month, the Food and Drug Administration limited its explicit approval of the updated covid-19 boosters to people over 65 or those with a higher risk of severe illness. The ACIP’s recommendation to move to an individualized approach, assuming it’s adopted by the CDC, may further delay or prevent people from obtaining a covid-19 booster if they so choose.

That said, several states like New York have already taken steps to ensure continued vaccine access and public coverage of the vaccine to all their residents. This week, the country’s largest health insurance association, America’s Health Insurance Plans, also announced that its members will rely on the previous ACIP recommendations to determine their coverage of the covid-19 vaccine for the time being. It additionally stated that patients covered by these plans would not experience cost-sharing through the end of 2026.

In a 6 to 6 vote, the ACIP declined to endorse a recommendation calling for people to require a prescription for the covid-19 vaccines—ACIP chairman Martin Kulldorff issued the tiebreaker, voting “no.”



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September 20, 2025 0 comments
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RFK Jr.’s Vaccine Panel Votes Down Its Own Proposal to Require Prescriptions for Covid-19 Shots
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RFK Jr.’s Vaccine Panel Votes Down Its Own Proposal to Require Prescriptions for Covid-19 Shots

by admin September 19, 2025


In another vote, advisers recommended adding language on the shot’s risks to the vaccine’s information sheet, which is already required by law.

The committee’s focus on Covid-19 vaccines reflects Kennedy’s long-held suspicion of them. Since taking office in February, Kennedy has canceled a half-billion dollars in mRNA vaccine research and separately ended a major contract with Moderna, one of the Covid vaccine manufactures, for work on a pandemic bird flu vaccine.

During Friday’s meeting, CDC scientists presented extensive data on the safety and efficacy of the Covid vaccines. They also explained in detail how the agency tracks Covid hospitalizations and said the agency has a “rigorous and standardized process” to determine whether hospitalizations are classified as being due to Covid-19.

During the discussion portion of the meeting, committee members made several unfounded claims. Robert Malone, a former mRNA researcher who has spread vaccine misinformation, questioned whether there is actually evidence of disease protection from the Covid shots. “Are there any well-defined, characterized correlates of protection for Covid, yes or no?” he demanded.

Cody Meissner, a pediatrician at Dartmouth College, responded that there is “a reasonable measurement of neutralizing or binding antibodies that correlate with protection against symptomatic infection in the first few months” after vaccination.

At one point, Hilary Blackburn, a pharmacist on the committee, questioned whether the Covid vaccine could be connected to her mother’s lung cancer diagnosis, which occurred two years after receiving a Covid vaccine. She said she is aware of four other individuals in her small hometown diagnosed with the same kind of cancer. “Is it related to the vaccine?” she asked.

In a tense exchange about potential birth defects associated with the Covid vaccines, some ACIP members pressed manufacturer Pfizer about eight birth defects that occurred in a group of pregnant women who received the company’s vaccine and two birth defects that occurred in an unvaccinated group. Alejandra Gurtman, who heads vaccine clinical research and development at Pfizer, replied that those rates are comparable to rates of congenital abnormalities seen in the general population.

Carol Hayes, a liaison with the American College of Nurse-Midwives who was present during the meeting, clarified that most birth defects arise during the first trimester of pregnancy, and in the cited study, mothers received the vaccine at 12 to 24 weeks of pregnancy.

At Friday’s meeting, the committee also reversed a decision it made just a day before. On Thursday, advisers voted to no longer recommend the combined measles, mumps, rubella, and varicella (MMRV) vaccine to children under age 4. Yet puzzlingly, it voted to maintain coverage of that vaccine through the federal Vaccines for Children program, which provides free vaccines to low-income children and those without insurance. On Friday, they voted that the program should not, in fact, cover it.

On Friday, advisers also voted 11 to one in favor of tabling a decision on whether to delay the birth dose of the hepatitis B vaccine until one month of age. The committee had discussed that vaccine extensively on Thursday, though it’s unclear why the committee was asked to look into the potential change at all, as the hepatitis B vaccine has been given to newborns in the US since 1991.

Infants get the vaccine before leaving the hospital because the virus can be passed from an infected mother to the baby during birth. Hepatitis B is a serious liver infection that can lead to cirrhosis and cancer. The vaccine is highly effective at preventing infection in newborns.

Chari Cohen, president of the Hepatitis B Foundation, tells WIRED there is no scientific rationale for delaying the hepatitis B vaccine until one month after birth and she worries about an increase in hepatitis B infections if the panel eventually recommends delaying the immunization.

“We will likely see more babies and young children who become infected,” Cohen says. “From a public health infrastructure perspective, we are concerned that this risk-based approach will miss preventing infection to babies born to infected moms.”

Up to 16 percent of HBV-positive pregnant women don’t get tested for hepatitis B, so screening doesn’t capture all infected mothers.

“We do not understand the motivation or rationale for this debate,” Cohen says.



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September 19, 2025 0 comments
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RFK Jr.’s Handpicked Vaccine Panel Nixes Measles-Chickenpox Combo for Kids Under 4
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RFK Jr.’s Handpicked Vaccine Panel Nixes Measles-Chickenpox Combo for Kids Under 4

by admin September 19, 2025


Robert F. Kennedy Jr.’s handpicked vaccine recommendation panel has just issued guidance that, if acted on, could overhaul when and how children receive vaccines designed to protect them from dangerous diseases like measles, rubella, and chickenpox.

The Advisory Committee on Immunization Practices (ACIP) met on Thursday. In an 8 to 3 vote, they recommended against the use of the combined measles, mumps, rubella, and varicella (chickenpox) vaccine in children under four. They are instead now recommending that children should only receive two separate vaccines covering these four diseases.

Kennedy’s new guard

The ACIP has traditionally been a panel of independent experts organized by the Centers for Disease Control and Prevention to help steer the country’s vaccine policy. Their recommendations, while non-binding, carry significant weight; many states mandate that children receive all the vaccines recommended by ACIP before entering public school, for instance. But under U.S. Health and Human Services Secretary Robert F. Kennedy, Jr., critics say that ACIP has become a platform for vaccine skepticism.

In early June, Kennedy unilaterally fired all 17 former members of ACIP and then, without any outside review, appointed eight new members, some of whom have previously misrepresented science on vaccine safety or who have financially benefited from attacking vaccines. Kennedy added five new members to the panel earlier this week, including some individuals who have questioned the safety and effectiveness of the covid-19 vaccines.

At the panel’s last meeting in June, in a majority vote, Kennedy’s new members recommended the removal of a mercury-based additive called thimerosal from the very few remaining vaccines that contain it. The recommendation was formally adopted by the government in July. Anti-vaccination proponents have long blamed thimerosal in vaccines for causing autism and other neurological conditions, even after it was phased out from all childhood shots two decades ago out of an abundance of caution. And dozens of studies have since failed to support any link between thimerosal (or, for that matter, any vaccine or specific ingredient) and autism.

Under Kennedy’s leadership, the CDC has been rocked by a series of high-profile departures. The Centers’ director Susan Monarez was reportedly fired for reportedly refusing to support Kennedy’s vaccine agenda—a decision that spurred the resignation of several other senior CDC staff and an unprecedented public display of support from remaining employees.

Monarez testified at a Senate hearing earlier this week, alleging that Kennedy had pressured her to rubber-stamp recommendations from ACIP. She also stated that Kennedy told her that the childhood vaccine schedule was going to change in September and that she needed to be “on board with it.”

What the latest vote means for these vaccines

In what was its second meeting since Kennedy dismissed the former members in June, the panel first debated the safety of the measles, mumps, rubella, and varicella (MMRV) vaccine.

The MMRV vaccine was approved in 2005 as a convenient alternative to children being given the MMR vaccine and a separate varicella vaccine, providing protection against all four diseases at once. Soon after its release to the public, however, evidence emerged that the first dose of the MMRV vaccine is associated with a slightly increased risk of febrile seizure (seizures caused by a fever) in children under the age of four as compared to the MMR plus varicella vaccine. Importantly, an additional risk of seizure wasn’t seen with the second dose of the MMRV vaccine given to older children.

The CDC was the first to discover and acknowledge this risk and has long recommended that, unless parents specifically request the MMRV vaccines, younger children should receive the MMR plus varicella vaccine as their first dose and the combined MMRV vaccine for the second dose. At Thursday’s ACIP meeting, CDC staff presented data showing that about 85% of parents choose the MMR and a separate varicella vaccine as recommended for the first dose. But since some families may prefer their children taking fewer vaccines overall, parents were advised they could opt for either vaccine strategy.

Febrile seizures are certainly scary for both the parent and for the child to experience. However, they’re generally short-lasting and aren’t often linked to longer-term health problems. In turn, the vast majority of these kinds of seizures aren’t tied to vaccination but to infections.

The long and short of it is that this change is wholly unnecessary, given that most parents take the CDC’s advice and don’t use the MMRV vaccine for the first dose. But the ACIP’s vote will effectively remove a family’s right to decide which shot their young children receive—an ironic fate given how anti-vaccination proponents often frame their decision to not vaccinate themselves or their children as an expression of freedom.

CDC staff noted that the ACIP’s recommendation could affect Medicaid coverage of these vaccines, as well as coverage offered through the Vaccines for Children (VFC) program, a federal program that provides vaccines to families unable to afford them. And it’s possible that some children who would have received the MMRV vaccine will end up not receiving the two separate vaccines for any number of reasons.

That said, the ACIP voted ‘No’ on whether the VFC should change its coverage in alignment with the new recommendation. This means that the program should stick to its existing coverage of the MMRV vaccine.

The ACIP also discussed whether it should continue to recommend universal hepatitis B vaccination starting at birth—a policy first endorsed by the group over 30 years ago. But due to a longer meeting than scheduled, the ACIP has delayed its vote on the matter until tomorrow. The ACIP is expected to weigh in on the covid-19 vaccines tomorrow as well.



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September 19, 2025 0 comments
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Vaccine Panel Stacked by RFK Jr. Recommends Delaying MMRV Immunization
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Vaccine Panel Stacked by RFK Jr. Recommends Delaying MMRV Immunization

by admin September 19, 2025


A federal vaccine advisory committee made up of members hand-picked by Health and Human Services secretary Robert F. Kennedy Jr. recommended in an 8-3 vote on Thursday that the combined measles, mumps, rubella, and varicella (MMRV) vaccine should not be given before age 4, citing long-known evidence that shows a slightly increased risk for febrile seizures in that age group.

Experts say that while frightening, febrile seizures—which are uncommon after vaccination—are usually short-lived and harmless, and removing the option for parents could cause a decline in immunization rates against measles, mumps, and rubella, some of the most dangerous childhood diseases.

Known as the Advisory Committee on Immunization Practices, or ACIP, the group provides recommendations to the US Centers for Disease Control and Prevention on vaccine usage. These recommendations are typically adopted by CDC and have an impact on state vaccine requirements for school, insurance coverage of vaccines, and pharmacy access—something at least one member of the panel seemed to be unaware of.

Thursday’s vote is part of a new shift in vaccine policy being spearheaded by Kennedy, a longtime anti-vaccine activist. In his short time as HHS secretary, Kennedy has implemented restrictions on who can receive Covid-19 vaccines and dismissed all 17 sitting members of ACIP, replacing them with 12 new members—some of whom were installed just this week. Several of the new advisers have a history of criticizing vaccines or denouncing public health measures taken during the Covid-19 pandemic. Kennedy said a “clean sweep” of ACIP was necessary to build back public confidence in vaccine science.

On Thursday, committee members were asked to evaluate whether to recommend against the combined MMRV vaccine before age 4, as well as whether to delay the first dose of the hepatitis B vaccine until the child is at least one month old.

Currently, parents have two options for vaccinating their children against measles, mumps, rubella, and varicella, also known as chickenpox. They can choose the combined shot, known as MMRV, or two separate shots—one for MMR and another for chickenpox. About 85 percent of children get separate shots.

In the US, the hepatitis B vaccine is given in the hospital shortly after birth, because the virus can be transmitted to children during delivery. A serious liver infection, hepatitis B can lead to cirrhosis and cancer. Each year in the US, an estimated 25,000 infants are born to women diagnosed with the hepatitis B virus. Without vaccination, up to 90 percent of them would develop chronic infections. The World Health Organization advises a universal birth dose of the hepatitis B vaccine.

The topics of discussion at Tuesday’s meeting were not based on new data or evidence, and in fact, two ACIP members, Joseph Hibbeln and Cody Meissner, as well as several representatives from professional medical organizations who were in attendance, questioned why these changes were up for consideration.

Robert Malone, one of the more controversial new ACIP members, offered an explanation: “It’s clear that a significant population of the United States has significant concerns about vaccine policy and about vaccine mandates.” Malone is a former mRNA researcher who rose to prominence during the Covid-19 pandemic by spreading falsehoods about the disease and the vaccines; he abstained from Thursday’s vote because he previously served as an expert witness in a lawsuit over the mumps vaccine.



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September 19, 2025 0 comments
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Fired CDC Director Says RFK Jr. Pressured Her to Blindly Approve Vaccine Changes
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Fired CDC Director Says RFK Jr. Pressured Her to Blindly Approve Vaccine Changes

by admin September 18, 2025


Debra Houry, former chief medical officer and deputy director for program and science at CDC, who was one of several agency officials to resign in the wake of Monarez’s firing, also testified during Wednesday’s hearing.

“I resigned because CDC leaders were reduced to rubber stamps, supporting policies not based in science, and putting American lives at risk. Secretary Kennedy censored CDC’s science, politicized its processes, and stripped leaders of independence. I could not and in good conscience, remain under those conditions,” Houry said.

She also accused Kennedy of halting flu campaigns despite the severity of the 2024-2025 flu season, as well as spreading misinformation and promoting unproven treatments for measles.

Houry said she learned that Kennedy had changed the CDC’s Covid-19 vaccine guidance from a social media post on X. “CDC scientists have still not seen the scientific data or justification for this change. That is not gold-standard science,” Houry said, referring to a statement in May that HHS will no longer recommend the vaccine for healthy children and pregnant women

Monarez said Secretary Kennedy had not communicated his plans to change the childhood vaccination schedule to her until their meeting on August 25. Monarez said she told Kennedy that she would be open to changing the childhood vaccine schedule if the evidence or science supported those changes. Kennedy responded that there was no existing science or evidence and elaborated that CDC had never collected that data, according to Monarez.

Monarez said she could not agree to approving ACIP recommendations before knowing what they were. “I have built a career on scientific integrity, and my worst fear was that I would then be in a position of approving something that would reduce access to life-saving vaccines to children and others who need them,” she said.

This Thursday, ACIP is set to discuss the hepatitis B vaccine, which has been recommended for newborns within 24 hours of birth since 1991. But the committee is expected to vote on removing that recommendation and delaying the birth dose of the hepatitis B vaccine until age 4.

Each year in the US, an estimated 25,000 infants are born to women diagnosed with the hepatitis B virus, or HBV, a serious liver infection that can lead to cirrhosis and cancer. Before the vaccine was introduced, nearly 20,000 babies and children were infected with HBV each year in the US. Now, fewer than 20 get the disease from their mothers.

“Now that we’ve controlled it, do we let the genie out of the bottle? If the recommendation goes away, and a parent does want the vaccine, insurance will no longer cover it free of charge. She’ll be forced to pay out of pocket,” Senator Cassidy said at the conclusion of the hearing. Vaccine coverage is typically tied to ACIP recommendations.

Cassidy was initially hesitant about Kennedy’s nomination as HHS secretary, given his prior statements about vaccines, but he supported him after, he has said, Kennedy promised to maintain vaccine availability and not undermine public trust in them.

ACIP is slated to discuss Covid-19 vaccines on Friday.



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September 18, 2025 0 comments
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Moderna CEO Responds to RFK Jr.’s Crusade Against the Covid-19 Vaccine
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Moderna CEO Responds to RFK Jr.’s Crusade Against the Covid-19 Vaccine

by admin September 9, 2025


At the WIRED Health summit on Tuesday, Moderna CEO Stéphane Bancel said the recent changes to Covid-19 vaccine policy made by Health and Human Services secretary Robert F. Kennedy, Jr. are a “step backward.”

Moderna is one of the manufacturers of mRNA-based Covid-19 vaccines, and last month the company received approval from the Food and Drug Administration for an updated version of the shot. But as part of that approval, the FDA imposed new restrictions on who can receive the vaccine. Previously, Covid vaccines were recommended for anyone 6 months or older. Now, the FDA says they should only be given to individuals at high risk of serious disease, either because they are 65 and older or have other health problems.

“I think it complicates things for people,” Bancel said. “You might have somebody in your household—a parent, a spouse, a kid—who is at high risk” that you want to protect, he said. Before, healthy individuals could just go to a pharmacy to receive a Covid shot. Now, several states require a prescription to get a Covid shot because of the FDA’s changes.

Kennedy has been on a crusade against vaccines since he stepped into the role of HHS secretary in February; earlier this week, the Senate Finance Committee grilled him about his actions in office so far.

In May, Kennedy terminated a $590 million contract with Moderna for the development of an mRNA-based bird flu vaccine candidate. The contract was awarded during the final days of the Biden administration in January, just before President Donald Trump’s second term began. Bird flu is widespread in wild birds and has been causing outbreaks in poultry and US dairy cows since March 2024. It has caused sporadic cases in people, most of them farm workers, but poses a pandemic potential if it develops the ability to spread from person to person.

That same month, Kennedy announced that HHS would no longer recommend mRNA Covid-19 vaccines for healthy children and pregnant women. In June, FDA said it would require new labels on mRNA vaccines to include safety information about the risks of myocarditis and pericarditis, rare side effects observed mostly in young men following administration of the shots.

In August, as a part of a “coordinated wind-down” of mRNA vaccine research, HHS canceled 22 related contracts and investments worth nearly $500 million. Kennedy incorrectly said in a statement these vaccines “fail to protect effectively against upper respiratory infections like Covid and flu.” HHS is instead shifting funding to an older vaccine platform known as “whole-virus” vaccines.

Despite the administration’s backlash against mRNA vaccines, Bancel said he is “encouraged by the dialogue” that the company has had with the FDA. In addition to getting updated Covid shots, albeit with limitations, Moderna also received expanded approval this year for its respiratory syncytial virus, or RSV, vaccine to include adults ages 18 to 59 who are at increased risk of disease. The vaccine was initially approved in May 2024 for adults aged 60 years and older.

“I think a lot of people back in January, including my own team, were quite worried that we might not get those approvals,” Bancel said.

The administration’s crackdown on mRNA research so far has not extended to the cancer space, and Moderna is developing several mRNA therapies against cancer, including personalized cancer vaccines. The company has 45 cancer-related programs in the pipeline, and has said it expects 10 FDA approvals in the next three years. “We are using exactly the same technology to go from infectious disease to cancer,” Bancel said.

He also addressed accusations that the Covid vaccines have not been well tested. “I don’t think there’s been a vaccine more studied for efficacy and safety in the history of vaccines,” he said. “In terms of vaccine efficacy and safety, there’s been studies done in literally millions of people in the real world.”



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September 9, 2025 0 comments
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