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Tag: United States Department of Health and Human Services

  • Trump administration said to reverse slashes in grants for mental health and addiction treatment programs

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    The Trump administration is said to to have suddenly reversed slashes in grants for mental health and addiction treatment programs that a source told CBS News were were valued at around $1.9 billion.

    Thousands of federal grants supporting the programs were suddenly terminated late Tuesday, sources told CBS News.

    The abrupt cancellations at the U.S. Substance Abuse and Mental Health Services Administration impacted 2,706 of the agency’s discretionary grants, a source familiar with the matter told CBS News. 

    President Trump’s political appointees moved to terminate the funding, not career officials working for SAMHSA, according to the source.

    But by Wednesday evening, those cuts were being reversed, according to reports in The New York Times, NPR, The Washington Post and others. Those three outlets say the restoration followed intense bipartisan backlash.

    CBS News has reached out to SAMHSA for comment.

    The top Democrat on the House Appropriations Committee, Rep. Rosa DeLauro, of Connecticut, said in a statement to the Times that the cuts should not have been made to begin with.

    The reason for the initial cuts wasn’t immediately clear.

    When the cuts were still being instituted, CBS News obtained a termination notice sent by a top SAMHSA official saying the agency was “terminating some of its awards in order to better prioritize agency resources” toward priorities “that address the rising rates of mental illness and substance abuse conditions, overdose, and suicide.”

    “This was not SAMSHA’s idea,” the CBS News source said, noting that many of the canceled grants addressed those priorities. “This was money going to people on the ground who are providing mental health treatment, substance use treatment, recovery support, and prevention resources, which this administration says is a priority.”

    SAMHSA, a branch of the Department of Health and Human Services, is at the forefront of efforts to improve mental health and address substance abuse across the country. At the national level, the agency leads public health initiatives geared toward reducing the burden of substance abuse and mental illness on communities, while also distributing funds to states and local entities for mental health and addiction services, according to its website

    A source said that among the grants that were being eliminated was one that provided $15 million per year to the Opioid Response Network, a program that offers evidence-based education and training to local authorities managing various types of substance use intervention, including prevention, treatment and recovery services. Another $6 million grant to a program called Building Communities of Recovery, which funds community-based resources to increase the availability and quality of long-term recovery support for people with substance use disorder, was being canceled as well.

    CBS News reached out to the Opioid Response Network and a representative for the Building Communities of Recovery program at SAMHSA.

    This latest funding loss was to follow the Trump administration’s sweeping Medicaid cuts that impacted a broad array of public health services including some focused on mental health and addiction. Those cuts were set to take effect in full later this year.

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  • RFK Jr.’s MAHA movement has picked up steam in statehouses. Here’s what to expect in 2026.

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    When one of Adam Burkhammer’s foster children struggled with hyperactivity, the West Virginia legislator and his wife decided to alter their diet and remove any foods that contained synthetic dyes.

    “We saw a turnaround in his behavior, and our other children,” said Burkhammer, who has adopted or fostered 10 kids with his wife. “There are real impacts on real kids.”

    The Republican turned his experience into legislation, sponsoring a bill to ban seven dyes from food sold in the state. It became law in March, making West Virginia the first state to institute such a ban from all food products.

    The bill was among a slew of state efforts to regulate synthetic dyes. In 2025, roughly 75 bills aimed at food dyes were introduced in 37 states, according to the National Conference of State Legislatures.

    Chemical dyes and nutrition are just part of the broader “Make America Healthy Again” agenda. Promoted by Health and Human Services Secretary Robert F. Kennedy Jr., MAHA ideas have made their deepest inroads at the state level, with strong support from Republicans — and in some places, from Democrats. The $50 billion Rural Health Transformation Program — created last year as part of the GOP’s One Big Beautiful Bill Act to expand health care access in rural areas — offers incentives to states that implement MAHA policies.

    Federal and state officials are seeking a broad swath of health policy changes, including rolling back routine vaccinations and expanding the use of drugs such as ivermectin for treatments beyond their approved use. State lawmakers have introduced dozens of bills targeting vaccines, fluoridated water, and PFAS, a group of compounds known as “forever chemicals” that have been linked to cancer and other health problems.

    In addition to West Virginia, six other states have targeted food dyes with new laws or executive orders, requiring warning labels on food with certain dyes or banning the sale of such products in schools. California has had a law regulating food dyes since 2023.

    Most synthetic dyes used to color food have been around for decades. Some clinical studies have found a link between their use and hyperactivity in children. And in early 2025, in the last days of President Joe Biden’s term, the Food and Drug Administration outlawed the use of a dye known as Red No. 3.

    Major food companies including Nestle, Hershey, and PepsiCo have gotten on board, pledging to eliminate at least some color additives from food products over the next year or two.

    “We anticipate that the momentum we saw in 2025 will continue into 2026, with a particular focus on ingredient safety and transparency,” said John Hewitt, the senior vice president of state affairs for the Consumer Brands Association, a trade group for food manufacturers.

    This past summer, the group called on its members to voluntarily eliminate federally certified artificial dyes from their products by the end of 2027.

    “The state laws are really what’s motivating companies to get rid of dyes,” said Jensen Jose, regulatory counsel for the Center for Science in the Public Interest, a nonprofit health advocacy group.

    Andy Baker-White, the senior director of state health policy for the Association of State and Territorial Health Officials, said the bipartisan support for bills targeting food dyes and ultraprocessed food struck him as unusual. Several red states have proposed legislation modeled on California’s 2023 law, which bans four food additives.

    “It’s not very often you see states like California and West Virginia at the forefront of an issue together,” Baker-White said.

    Although Democrats have joined Republicans in some of these efforts, Kennedy continues to drive the agenda. He appeared with Texas officials when the state enacted a package of food-related laws, including one that bars individuals who participate in the Supplemental Nutrition Assistance Program — SNAP, or food stamps — from using their benefits to buy candy or sugary drinks. In December, the U.S. Department of Agriculture approved similar waivers sought by six states. Eighteen states will block SNAP purchases of those items in 2026.

    There are bound to be more. The Rural Health Transformation Program also offers incentives to states that implemented restrictions on SNAP.

    “There are real and concrete effects where the rural health money gives points for changes in SNAP eligibility or the SNAP definitions,” Baker-White said.

    In October, California Gov. Gavin Newsom signed a bill that sets a legal definition for ultraprocessed foods and will phase them out of schools. It’s a move that may be copied in other states in 2026, while also providing fodder for legal battles. In December, San Francisco City Attorney David Chiu sued major food companies, accusing them of selling “harmful and addictive” products. The lawsuit names specific brands — including cereals, pizzas, sodas, and potato chips — linking them to serious health problems.

    Kennedy has also blamed ultraprocessed foods for chronic diseases. But even proponents of the efforts to tackle nutrition concerns don’t agree on which foods to target. MAHA adherents on the right haven’t focused on sugar and sodium as much as policymakers on the left. The parties have also butted heads over some Republicans’ championing of raw milk, which can spread harmful germs, and the consumption of saturated fat, which contributes to heart disease.

    Policymakers expect other flash points. Moves by the FDA and the Centers for Disease Control and Prevention that are making vaccine access more difficult have led blue states to find ways to set their own standards apart from federal recommendations, with 15 Democratic governors announcing a new public health alliance in October. Meanwhile, more red states may eliminate vaccine mandates for employees; Idaho made them illegal. And Florida Gov. Ron DeSantis is pushing to eliminate school vaccine mandates.

    Even as Kennedy advocates eliminating artificial dyes, the Environmental Protection Agency has loosened restrictions on chemicals and pesticides, leading MAHA activists to circulate an online petition calling on President Donald Trump to fire EPA Administrator Lee Zeldin.

    Congress has yet to act on most MAHA proposals. But state lawmakers are poised to tackle many of them.

    “If we’re honest, the American people have lost faith in some of our federal institutions, whether FDA or CDC,” said Burkhammer, the West Virginia lawmaker. “We’re going to step up as states and do the right thing.”

    KFF Health News is a national newsroom that produces in-depth journalism about health issues and is one of the core operating programs at KFF — the independent source for health policy research, polling, and journalism.

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  • 5 states sue Trump administration for freezing social services funding

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    Attorneys general in five Democratic-led states filed a lawsuit Thursday against the Trump administration after it said it would freeze money for several public benefit programs, citing concerns about fraud in the programs designed to help low-income families.

    The states — California, Colorado, Minnesota, Illinois and New York — called the move an unconstitutional abuse of power. The Trump administration announced earlier this week it was withholding their social safety net funding. The funding went toward three federal programs, two of which focus on lifting families with children out of poverty.

    New York Attorney General Letitia James, who is leading the lawsuit, said the Trump administration is overstepping its authority by freezing billions of dollars in funds that were already approved for the states by Congress.

    The lawsuit filed in the U.S. District Court for the Southern District of New York asks the courts to order the administration to halt the freeze and release the funds.

    “Once again, the most vulnerable families in our communities are bearing the brunt of this administration’s campaign of chaos and retribution,” James said.

    The U.S. Department of Health and Human Services this week told the five states it was freezing their money for the Child Care and Development Fund, which subsidizes childcare for children from low-income families; the Temporary Assistance for Needy Families program, which provides cash assistance and job training; and the Social Services Block Grant.

    HHS officials did not immediately respond to a request for comment on the lawsuit.

    In an interview with CBS News Wednesday, Health and Human Services Secretary Robert F. Kennedy Jr. because they wouldn’t show the Trump administration plans for eliminating fraud. 

    “The best way to help poor families is to end the fraud,” he told CBS News. Kennedy said the five states were impacted, not because they’re run by Democrats, but because they “refuse to cooperate with developing plans that would end the fraud.”

    “We gave them a warning,” Kennedy said of the five states, claiming that the administration told them they wouldn’t cut funding if they presented a plan for handling fraud.

    “But if you won’t show us a plan, a workable plan, we’re gonna cut it off until you do,” he said.

    When asked how long the funding will be cut off, Kennedy replied, “That’s up to them.”

    About half of the $10 billion in funding targeted by the Trump administration supported California programs, said the state’s attorney general, Rob Bonta.

    In letters to the states, Alex J. Adams, assistant secretary for the Administration for Children and Families, wrote that HHS had “reason to believe” the states were providing benefits to people who were in the U.S. illegally, offering no further details about the allegations. They requested reams of data, including the names and Social Security numbers of everyone that had received some of the benefits.

    “The letters requested that California turn over essentially every document ever associated with the state’s implementation of these federal programs and do so within 14 days, by Jan. 20, including personally identifiable information about program participants,” Bonta said. “That is deeply concerning and also deeply frustrating.”

    The government intensified its focus on the childcare subsidy program after a conservative YouTuber released a video claiming day care centers in Minneapolis had committed up to $100 million in fraud. The childcare centers were run by members of the city’s Somali community, which has been frequently maligned by President Trump and targeted by immigration authorities.

    Minnesota Gov. Tim Walz, a Democrat, has defended his state’s response and said his state is taking aggressive action to prevent further fraud.

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  • RFK Jr.’s new food pyramid emphasizes protein, healthy fats. Here’s what to know about the dietary guidelines.

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    The Trump administration has unveiled a new food pyramid and dietary guidelines for Americans that call for “prioritizing high-quality protein, healthy fats, fruits, vegetables and whole grains” while avoiding highly processed foods and refined carbohydrates. 

    “As secretary of Health and Human Services, my message is clear: Eat real food,” HHS Secretary Robert F. Kennedy Jr. said at a White House briefing announcing the changes alongside Agriculture Secretary Brooke Rollins and other health officials. Kennedy called it “the most significant reset of federal nutrition policy in history.”

    A White House official told CBS News the new guidelines are “science-driven.” In a fact sheet, the administration said the new guidelines would restore “science and common sense” and put “real food back at the center of health.” 

    Here’s what to know about the new dietary guidelines. 

    First recommended limits on highly processed foods

    For the first time, the recommendations are calling for Americans to avoid eating highly processed foods

    A recent report from the Centers for Disease Control and Prevention found that 55% of the U.S. population receives more than half of their daily calories from ultra-processed foods. The previous 2020-2025 dietary guidelines did not mention highly processed or ultra-processed foods.

    The new guidelines call for avoiding “highly processed packaged, prepared, ready-to-eat, or other foods that are salty or sweet,” as well as avoiding sweetened beverages including soda, fruit drinks and energy drinks. 

    Research has shown diets high in ultra-processed food are associated with an increased risk of 32 damaging health outcomes, according to a review published in The BMJ medical journal in 2024.

    Limits on sugars, artificial flavors and dyes

    The guidelines also say that “no amount of added sugars” are recommended for Americans, especially children. 

    At most, a meal should contain no more than 10 grams of added sugars, according to the new guidance. The former guidance said children under 2 should not consume added sugars and that Americans should aim to have less than 10% of their daily calories come from added sugars. 

    People should also limit foods and beverages that include artificial flavors, dyes, low-calorie non-nutritive sweeteners and artificial preservatives, the new guidelines said. 

    Naturally occurring sugars are not considered added sugars and can be part of a recommended diet under the new guidelines. 

    Fighting chronic disease and supporting gut health 

    Dietary guidelines are used as the baseline for federal food programs, including SNAP and school meal programs. The fact sheet for the new guidelines says public adherence to the new guidelines “will dramatically lower chronic disease — and healthcare costs — for Americans.” 

    The fact sheet said the U.S.’s high level of health-related spending and a life expectancy that is five years less than other developed countries is “predominantly due to chronic conditions tied to food.” It also said that lowering rates of obesity, Type 2 diabetes, heart disease and Alzheimer’s disease would cut about $600 billion in annual healthcare costs. Previous studies have also shown a possible link between diet and Alzheimer’s

    “The most expensive thing we can do as a country is continue government incentives for food that sickens Americans and drives up healthcare costs,” the fact sheet said. 

    The new guidelines point out the importance of gut health and the microbiome inside a person’s intestines. The gut microbiome includes trillions of bacteria, viruses and fungi whose balance is important for good health. The new guidelines call for the consumption of vegetables, fruits, fermented foods and high-fiber foods to support a diverse gut microbiome. 

    “Ending the war on healthy fats”

    The fact sheet for the new guidance calls for “ending the war on healthy fats” and getting the bulk of dietary fats from whole food sources. That includes meat, poultry, eggs, seafood, nuts, full-fat dairy and avocados, the guidelines say. 

    People should aim for three servings of dairy a day, in line with the 2020-2025 guidelines. The new guidelines say people should prioritize full-fat options, while the previous guidelines recommended fat-free or low-fat products. 

    The new guidelines also recommend olive oil, butter or beef tallow for preparing meals. Kennedy has previously criticized seed oils and extolled tallow, at odds with long-standing recommendations. 

    “We are ending the war on saturated fats,” Kennedy said. 

    In total, saturated fat consumption should not exceed more than 10% of a person’s daily calories, according to the new guidelines. The 2020-2025 guidelines also had similar recommended limits on saturated fats, though they noted a “healthy dietary pattern” could include vegetable oils. 

    A focus on protein and “real” foods 

    The new guidelines recommend “high-quality, nutrient dense protein foods” including eggs, poultry, seafood, red meat, and plant-based proteins like beans, nuts and seeds in every meal. 

    Under the guidelines, Americans should aim to eat 1.2 to 1.6 grams of protein per kilogram of body weight every day. Proteins should be served with no or limited added sugars, chemical additives, refined carbohydrates or starches, the guidelines say. 

    “What we’re stressing is that people should be eating protein,” Kennedy said in an interview with CBS News chief White House correspondent Nancy Cordes.

    FDA Commissioner Marty Makary noted at the briefing that the new guidelines increase the recommended amount of protein for children.

    “Kids need protein,” Makary said. “The old protein guidelines were to prevent starvation and withering away. These new protein guidelines are designed for American kids to thrive.”

    Fruits, vegetables and whole grains

    The new guidelines also recommend people eat at least three servings of vegetables and two servings of fruit per day, in line with the previous 2020-2025 dietary guidance. 

    People should eat a variety of fruits and vegetables, preferably in their original form. Frozen, dried or canned products with no or very limited added sugars “can also be good options,” according to the fact sheet. People should limit consumption of 100% fruit or vegetable juices. 

    Americans should also prioritize fiber-rich whole grains and reduce the consumption of highly processed, refined carbs, the guidelines say. People should aim for between two and four servings of whole grains per day.  

    A new food pyramid

    Officials released a new version of the food pyramid, with protein, dairy, healthy fats making up one of the top corners, fruits and vegetables in the other, and whole grains at the bottom.

    A new version of the food pyramid was released by the USDA and Department of Health and Human Services on Jan. 7, 2026.

    USDA/Department of Health and Human Services


    Consume less alcohol

    The guidelines recommend that Americans should “consume less alcohol for better overall health.”

    People in certain categories are urged to completely avoid alcohol, including pregnant women, people who are recovering from alcohol use disorder or are unable to control the amount they drink, and people taking medications or with medical conditions that can interact with alcohol. 

    Previous guidelines said that Americans should not drink or drink in moderation. The recommended limits were 2 drinks or less per day for men and 1 drink or less per day for women on days when alcohol is consumed. 

    Dr. Mehmet Oz, administrator for the Centers for Medicare and Medicaid Services, said the new guidelines are meant to encourage moderation but acknowledge the social benefits that some may experience. 

    “There is alcohol on these guidelines, but the implication is don’t have it for breakfast,” Oz said.  

    Reactions to new dietary guidance 

    The American Medical Association said in a statement that it “applauds” the Trump administration’s new dietary guidelines.

    “The guidelines affirm that food is medicine and offer clear direction patients and physicians can use to improve health,” Dr. Bobby Mukkamala, the president of the AMA, said in the statement. Kennedy thanked Mukkamala in his briefing. 

    The AMA said it will launch a collection of educational resources and hold a series of roundtable discussions with doctors and experts to “strengthen nutrition education and clinical competency.” It also pledged to work with Congress to incentivize the consumption of nutrient-dense foods, expand food labeling efforts, define ultra-processed foods and increase investment in nutrition research. 

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  • HHS freezes all child care payments to Minnesota after viral fraud allegations

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    The Department of Health and Human Services said Tuesday it has frozen federal child care funding for the state of Minnesota, citing viral fraud allegations.

    Deputy HHS Secretary Jim O’Neill announced the move in a post on X, writing that “blatant fraud … appears to be rampant in Minnesota and across the country.” 

    “We have turned off the money spigot and we are finding the fraud,” he wrote.

    O’Neill cited a video in which conservative YouTuber Nick Shirley alleged nearly a dozen Minnesota day care centers that receive state funds aren’t actually providing services. O’Neill said the agency has identified the centers mentioned in a video and demanded that the state carry out a “comprehensive audit” of them, including “attendance records, licenses, complaints, investigations and inspections.”

    CBS News conducted its own analysis of day care centers mentioned by Shirley. All but two have active licenses, according to state records, and all active locations were visited by state regulators within the last six months. The analysis found dozens of citations for safety, cleanliness and other issues, but no recorded evidence of fraud.

    Some of the day care centers featured in Shirley’s video have pushed back against the fraud allegations. One of the facilities, ABC Learning Center, shared surveillance videos with CBS News that showed parents dropping children off on the same day as Shirley’s visit.

    A spokesperson for Minnesota Gov. Tim Walz said in a statement: “The governor has been combating fraud for years while the President has been letting fraudsters out of jail.  Fraud is a serious issue. But this is a transparent attempt to politicize the issue to hurt Minnesotans and defund government programs that help people.”

    Starting immediately, O’Neill said, all payments from HHS’s Administration for Children and Families nationwide “will require a justification and a receipt or photo evidence before we send money to a state.”

    The Administration for Children and Families sends some $185 million in child care funds to Minnesota annually, the agency’s head, Alex Adams, said in a video shared by HHS.

    Minnesota receives hundreds of millions of federal dollars per year to support its Child Care Assistance Program, which subsidizes day care services for roughly 23,000 children from low-income families. In the current fiscal year ending in September 2026, the federal government’s share of the program was expected to total $218 million, with the state kicking in $155 million, according to state projections.

    The moves by O’Neill came one day after agents from the Department of Homeland Security visited dozens of sites in Minneapolis, part of what DHS Secretary Kristi Noem described as a “massive investigation on child care and other rampant fraud.”

    In recent years, Minnesota has grappled with a litany of alleged fraud schemes targeting the state’s public assistance programs. Dozens of people have been convicted as part of a scheme to bilk nearly $250 million from a federally backed child nutrition program during the pandemic, and federal prosecutors have charged people with defrauding Medicaid-supported autism services and housing stabilization programs.

    Federal prosecutors have estimated that fraudulent payments made by Minnesota’s Medicaid service in recent years could total $9 billion or more, a figure that Walz has disputed.

    The fraud issues have drawn the attention of President Trump, who has focused on the fact that many — though not all — of the defendants are of Somali descent.

    Walz has defended the state’s handling of the situation but vowed to crack down on fraud.

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  • HHS freezes all federal child care funding to Minnesota in wake of fraud claims

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    HHS freezes all federal child care funding to Minnesota in wake of fraud claims – CBS News









































    Watch CBS News



    The Department of Health and Human Services said it has frozen federal child care funding for the state of Minnesota, citing viral fraud allegations. Jonah Kaplan has the latest.

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  • 19 states and D.C. sue HHS over effort to ban transgender care for minors

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    A coalition of 19 states and the District of Columbia on Tuesday sued the U.S. Department of Health and Human Services, its secretary, Robert F. Kennedy Jr., and its inspector general over a declaration that could complicate access to gender-affirming care for young people.

    The declaration issued last Thursday called treatments like puberty blockers, hormone therapy and surgeries unsafe and ineffective for children and adolescents experiencing gender dysphoria, or the distress when someone’s gender expression doesn’t match their sex assigned at birth. It also warned doctors that they could be excluded from federal health programs like Medicare and Medicaid if they provide those types of care.

    The declaration came as HHS also announced proposed rules meant to further curtail gender-affirming care for young people, although the lawsuit doesn’t address those as they are not final.

    Tuesday’s lawsuit, filed in U.S. District Court in Eugene, Oregon, alleges that the declaration is inaccurate and unlawful and asks the court to block its enforcement. It’s the latest in a series of clashes between an administration that’s cracking down on transgender health care for children, arguing it can be harmful to them, and advocates who say the care is medically necessary and shouldn’t be inhibited. After taking office in January, President Trump signed an executive order that seeks to cut federal support for certain types of gender-affirming care for people under the age of 19. 

    “Secretary Kennedy cannot unilaterally change medical standards by posting a document online, and no one should lose access to medically necessary health care because their federal government tried to interfere in decisions that belong in doctors’ offices,” New York Attorney General Letitia James, who led the lawsuit, said in a statement Tuesday.

    The lawsuit alleges that HHS’s declaration seeks to coerce providers to stop providing gender-affirming care and circumvent legal requirements for policy changes. It says federal law requires the public to be given notice and an opportunity to comment before substantively changing health policy — neither of which, the suit says, was done before the declaration was issued.

    A spokesperson for HHS declined to comment.

    HHS’s declaration based its conclusions on a peer-reviewed report that the department conducted earlier this year that urged greater reliance on behavioral therapy rather than broad gender-affirming care for youths with gender dysphoria.

    The report questioned standards for the treatment of transgender youth issued by the World Professional Association for Transgender Health and raised concerns that adolescents may be too young to give consent to life-changing treatments that could result in future infertility.

    Major medical groups and those who treat transgender young people have sharply criticized the report as inaccurate, and most major U.S. medical organizations, including the American Medical Association, continue to oppose restrictions on transgender care and services for young people.

    The declaration was announced as part of a multifaceted effort to limit gender-affirming health care for children and teenagers — and built on other Trump administration efforts to target the rights of transgender people nationwide.

    HHS on Thursday also unveiled two proposed federal rules — one to cut off federal Medicaid and Medicare funding from hospitals that provide gender-affirming care to children, and another to prohibit federal Medicaid dollars from being used for such procedures.

    The proposals are not yet final or legally binding and must go through a lengthy rulemaking process and public comment before becoming permanent. But they will nonetheless likely further discourage health care providers from offering gender-affirming care to children.

    Several major medical providers already have pulled back on gender-affirming care for young patients since Mr. Trump returned to office — even in states where the care is legal and protected by state law.

    Medicaid programs in slightly less than half of states currently cover gender-affirming care. At least 27 states have adopted laws restricting or banning the care. The Supreme Court’s recent 6-3 decision upholding Tennessee’s ban means most other state laws are likely to remain in place. The case, U.S. v. Skrmetti, marked the first time the Supreme Court had waded into the issue of health care for transgender youth. 

    Tennessee’s law prohibits medical treatments like puberty blockers or hormone therapy for transgender adolescents under the age of 18.  

    The state had argued that it has a “compelling interest in encouraging minors to appreciate their sex, particularly as they undergo puberty,” and in barring treatments that “might encourage minors to become disdainful of their sex.”   

    “Our role is not ‘to judge the wisdom, fairness, or logic’ of the law before us, but only to ensure that it does not violate the equal protection guarantee of the Fourteenth Amendment. Having concluded it does not, we leave questions regarding its policy to the people, their elected representatives, and the democratic process,” Chief Justice John Roberts wrote for the majority.  

    Joining James in Tuesday’s lawsuit were Democratic attorneys general from California, Colorado, Connecticut, Delaware, Illinois, Maine, Maryland, Massachusetts, Michigan, Minnesota, New Jersey, New Mexico, Oregon, Rhode Island, Vermont, Wisconsin, Washington and the District of Columbia. Pennsylvania’s Democratic governor also joined.

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  • RFK Jr. says he’ll work with federal agencies to wind down animal testing

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    Health and Human Services Secretary Robert F Kennedy Jr. said this weekend that he is working across the government to end all federally funded animal testing. 

    “All the major agency heads are committed to ending animal experimentation,” he said in an interview with Lara Trump on Fox News, referring to research being conducted by the U.S. Centers for Disease Control and Prevention and the National Institutes of Health. 

    Kennedy focused specifically on monkey testing, or “non-human primate testing,” during his remarks. There are over 100,000 monkeys in primate testing labs around the country, with more than 20,000 more being imported every year, he said. 

    “We are trying to put an end to that,” Kennedy said.

    Earlier this year, a CBS News investigation with the South Carolina Post & Courier documented efforts to cancel nearly $28 million in federal grants for research that relied on animals. And it found that, as federal health agencies moved to phase out research on live primates, available alternatives were not yet ready for use.

    It was against this backdrop that scientists at the CDC were ordered last month to phase out all their monkey research, a directive first reported in the journal Science

    “Across the Trump Administration, there is a shift to prioritize animal welfare,” a health department spokesperson told CBS News in a statement. “At HHS, that includes moves to reduce unnecessary animal testing requirements and prioritizing human-based research.” 

    Primate testing has been an integral part of medical advancement for nearly a century, and federal regulations require that most pharmaceuticals be tested on primates before they enter human clinical studies. Experiments on monkeys are credited with major medical advancements leading to the creation of Tylenol, the COVID-19 vaccine and Ozempic, among other things.  

    Experiments on primates make up a small portion of biomedical research overall, but Deborah Fuller, director of the NIH-funded Washington National Primate Research Center, said they are essential for developing therapies that continue to save lives. 

    “The majority of the biomedical interventions that we have today went through a non-human primate at some point,” she said. “Shutting down a non-human primate research program, you’re actually shooting yourself in the foot.”

    A view of primates in cages in a research facility n Yemassee, South Carolina, on Nov. 8, 2024. 

    Peter Zay/Anadolu via Getty Images


    For example, 200 primates are part of CDC’s ongoing research into treatments for HIV and other infectious diseases. Non-human primates are the only animals that closely model HIV infection in humans, according to Fuller. 

    “It is a very small slice of all of the animal research that’s done. And it is only done because that is the only model that can effectively answer the question that’s being addressed,” she said.

    But animal rights groups, who have found allies in the Trump administration, say this type of testing is outdated. 

    “I think it’s baseless fear-mongering to suggest we need to torture animals to improve human health. All of the available evidence suggests otherwise,” said Justin Goodman, senior vice president of advocacy and public policy at White Coat Waste Project. The organization

    advocates to end all federally funded animal testing and works closely with the Trump administration to cut grant programs that rely on it. 

    Kennedy’s pledge was “unprecedented,” Goodman said.

    “As the head of the agency that funds more animal testing than anyone else in the world, RFK’s commitment to ending testing on primates and other animals is game-changing,” he said. “We are optimistic — but the devil is in the details.” 

    The details for how the federal government intends to actually end animal testing remain sparse. The fate of monkeys already in labs across the country is also unclear.

    Kennedy said his agency is exploring options to retire animals to sanctuaries. But there are limited facilities equipped to take in the thousands of primates that may need continued medical monitoring. The estimated cost of transporting the animals alone could cost millions of dollars, even if there were available space for the animals in question. 

    “We need to make sure we have space somewhere that can take care of these animals for the rest of their lives,” said Sally Thompson-Iritani, an associate professor at the University of Washington, who helps oversee the university’s animal care program. “And we currently don’t have an infrastructure that supports that.”

    “I think there’s legitimately logistical issues that have to be sorted out, which is why we are anxious to hear more details from HHS about what its plans are,” Goodman agreed, calling such an effort “a massive undertaking.”

    Moreover, some animals that have been infected with dangerous diseases like Ebola would not be able to move to a sanctuary and would likely need to be euthanized, Goodman said. 

    Kennedy has pushed for alternatives to animal testing, suggesting that AI and computer generated models are more accurate and efficient methods for predicting health outcomes in humans. The FDA and NiH put out updated guidelines advocating for the phasing out of live animal models in favor of alternative technologies this spring. 

    But researchers on the cutting edge of these alternatives don’t believe that the new technologies are ready to completely replace primate models. 

    “I want to see us get out of the business of using animals in research,” said Paul Locke in an interview with CBS News over the summer. Locke is an environmental health lawyer at Johns Hopkins Bloomberg School of Public Health and serves on the board of the school’s Center for Alternatives to Animal Testing. 

    “The question is when. When can we do that and reach the double goal of having better science and virtually no animals? The answer is not tomorrow.”

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  • Kennedy sharpens vaccine attacks, without scientific backing

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    As the federal government prepares for the next meeting of its Advisory Committee on Immunization Practices, Health and Human Services Secretary Robert F. Kennedy Jr. has intensified his attacks on aluminum vaccine components used in many shots to boost the body’s immune response.

    Kennedy, a longtime anti-vaccine activist before seeking public office, claims that aluminum adjuvants are neurotoxic and tied to autism, asthma, autoimmune disease, and food allergies.

    But science and medicine advances a different view. Strong recommendations that parents introduce peanut-containing foods to infants early, for instance, have led to a drop in the incidence rate of peanut allergies.

    Since taking office, Kennedy has ordered reviews of vaccine ingredients, citing aluminum as a top concern. A discussion of “adjuvants and contaminants” is on the vaccine advisory panel’s draft agenda.

    A Centers for Disease Control and Prevention webpage that for years has assured the public vaccines do not cause autism was updated Nov. 19 with new language stating that studies have not definitively ruled out a link between vaccines and autism.

    He has also targeted scientists who have published studies showing aluminum adjuvants are safe. In August, Kennedy denounced a large Danish study finding no link between aluminum in vaccines and childhood disease, calling it a “deceitful propaganda stunt” and demanding its retraction. The Annals of Internal Medicine rejected the claim and refused to retract the study.

    And, regarding the upcoming advisory panel meeting, HHS spokesperson Emily HIlliard said ACIP “is independently reviewing the full body of evidence on adjuvants and other vaccine components to ensure the highest safety standards.”

    The stakes are high because Kennedy’s push to cast doubt on aluminum isn’t just about the ingredient itself. It’s part of a broader strategy to foster uncertainty about vaccine safety and lay the groundwork to challenge the National Vaccine Injury Compensation Program, which drug manufacturers say is essential to ensure a stable market for shots.

    But researchers across infectious diseases, immunology, pediatrics, and epidemiology say the data is clear: Aluminum adjuvants are safe.

    “Aluminum is the third most common element on the Earth’s surface,” said Dr. Paul Offit, a pediatrician and director of the Vaccine Education Center at Children’s Hospital of Philadelphia. “So we’re all exposed to aluminum all the time. The water that we drink has aluminum in it. The food that we eat has aluminum in it.”

    Vaccines add only a tiny amount of aluminum to the body — a combined total of about 8 milligrams — after the schedule of childhood vaccines is complete. Offit said that over the first 18 years of life, people naturally take in about 400 milligrams of aluminum from everyday sources.

    “I don’t know why there is so much concern,” said Dr. Rajesh Gupta, a former FDA vaccine scientist. “Aluminum gets distributed in the body everywhere. It is ultimately excreted by the kidneys in the urine. So, it is not that aluminum stays in the body.”

    How they work

    The aluminum in vaccines isn’t foil or metal. It’s a compound of aluminum salts, such as aluminum hydroxide or aluminum phosphate, that help the vaccine work better.

    It’s a bit like zinc in cold tablets: Patients don’t swallow chunks of metal, instead ingesting a zinc salt that dissolves safely in the body.

    In vaccines, these aluminum salts give the immune system an extra nudge so it learns to recognize the target germ more effectively.

    When injected, the vaccine stays near the injection site and causes mild, short-lived inflammation that summons immune cells. Those cells pick up the vaccine antigen, a harmless piece of a virus or bacterium, and carry it to nearby lymph nodes. There, the adjuvants show it around like a wanted poster so the body can identify and destroy the germ quickly.

    Dr. Harm HogenEsch, a professor of immunopathology at the Purdue University College of Veterinary Medicine, said that aluminum adjuvants work only when they’re injected in the same spot as the vaccine ingredient they’re meant to boost, to help nearby immune cells learn to recognize the germ. If the two shots are given in different places, he said, “you don’t see that effect.”

    In response to Kennedy’s claims, scientists say that anything that acts as an adjuvant can, in principle, also boost an allergic response. But that doesn’t mean aluminum-adjuvanted vaccines are turning children into food-allergic time bombs. Antigens in vaccines such as the hepatitis B surface antigen or HPV proteins are not allergens, and no food proteins are put into vaccines.

    Animal experiments

    Animal studies form the basis of Kennedy’s claim that aluminum adjuvants in vaccines can create allergies. In these experiments, scientists deliberately sensitize rats or mice by injecting them with a food protein mixed with aluminum. The aluminum strengthens the immune response, but it does not cause an allergy by itself.

    “That’s the basis for a lot of the experimental mouse models, where you inject a food allergen with an aluminum adjuvant to sensitize the mice,” HogenEsch said. “I’m not aware of any food antigen being included in vaccines, and so I don’t really see a way by which this could happen.”

    Dr. Ross Kedl, a professor of immunology and microbiology at the University of Colorado Anschutz School of Medicine, went further, noting that there is no plausible route for vaccines to create a peanut allergy out of thin air. “Someone would have had to mix peanut proteins in with the actual vaccine prior to injection.”

    Dr. Stefan H. E. Kaufmann, director emeritus at the Max Planck Institute for Infection Biology in Berlin, said results from mice often don’t match what happens in people, because “mice are much easier to push into allergic reactions than humans.” In other words, what looks dramatic in a rodent study doesn’t automatically apply to human immune systems.

    And in this case, it’s “important to distinguish between how aluminum behaves in lab animals versus people,” Kaufmann said.

    Human studies

    Beyond animal models and theoretical scenarios, scientists have looked hard for signals of harm in large human datasets.

    In 2023, a study by the Vaccine Safety Datalink, a collaboration coordinated by the CDC, reported a slight increase in asthma among children with higher aluminum exposure before age 2, but the association disappeared in further analyses.

    “That paper was roundly criticized,” Offit said. “When they controlled for breastfeeding, the association between asthma and receipt of aluminum-adjuvant-containing vaccines disappeared.”

    “It should have never been published,” he said.

    Dr. Kathy Edwards, professor emerita of pediatrics at Vanderbilt University, said that false signals are common when large databases are mined for dozens of outcomes.

    “When you look at a hundred different things, just by the law of percentages, some of those may look like there is a signal,” she said. “The whole RFK Jr. assessment is really prone to cherry-picking,” she said, adding that “there does need to be some kind of basic understanding of statistics for people to interpret this.”

    Soon after the 2023 U.S. findings drew attention, scientists at the CDC contacted Dr. Anders Hviid, head of epidemiology research at the Statens Serum Institut in Copenhagen, Denmark, to see whether his team could replicate the work.

    “It makes perfect sense to try to replicate findings of any kind in different data sources,” Hviid said.

    Hviid’s nationwide Danish study followed 1.2 million children over two decades, using linked national health registries that record every vaccination and diagnosis.

    “Our health care system is quite egalitarian. It’s free, and there’s universal access. And everyone is in these nationwide registers,” he said. Their findings: no increased risk of these conditions associated with increasing amounts of aluminum received through the vaccines.

    Rare bumps

    Doctors have documented one genuine reaction to aluminum adjuvants: itchy nodules at the injection site, called “pruritic granulomas.” These small bumps are so rare that most allergists and pediatricians will never see a single case.

    This reaction “doesn’t lead to something bad, and it really isn’t associated with anything other than that local irritation,” Edwards said.

    Researchers believe these bumps represent a localized immune response — meaning only in the area of the injection, not a body-wide allergy — that is very different from the kind of immediate allergic reaction people treat with antihistamines. These include the reactions driven by food or beestings, when histamine, the body’s own alarm signal, floods the system within minutes and causes hives, swelling, or breathing trouble. Kedl said that distinction often gets lost in public debate.

    Eliminating aluminum adjuvants

    For many experts, the real issue is not just whether aluminum is safe but what happens to the entire vaccine program if aluminum adjuvants are stripped out. For many modern vaccines that rely on a single purified protein — such as those for diphtheria and tetanus toxoids, hepatitis B, and HPV — adjuvants are crucial.

    Edwards said that simply swapping in a different adjuvant isn’t realistic.

    “They’re kind of all built on one another,” she said. Once a vaccine has been proved to work and become the standard of care, new or updated versions are generally no longer tested against a placebo in people who should be getting that vaccine. Instead, they’re tested against the existing product, which means each approval rests on the one before it.

    Core childhood vaccines would probably have to be reformulated, and large clinical trials would have to be repeated to prove the new products are safe and effective. Meanwhile, production gaps and shortages would have to be managed, potentially for years, while manufacturers and regulators start over — all while diseases such as whooping cough, hepatitis B, and HPV-related cancers gain more room to spread.

    “The aluminum adjuvants have sort of hit the sweet spot in terms of being effective at inducing a robust antibody response that is protective for those vaccines in which they’re being used and being very safe,” HogenEsch said. “It would be quite frankly foolish to try to eliminate them.”

    A century of safe use

    The DTaP, hepatitis B, and HPV vaccines all contain aluminum adjuvants and have been in use for nearly a century. Large-scale studies show no link between aluminum and systemic allergic disease.

    “We have had aluminum adjuvants in vaccines for decades,” Edwards said. “I have grandchildren. My grandchildren have received all of their vaccines. And I do not worry about the safety of them.”

    If aluminum is falsely cast as the villain and vaccine uptake falls, experts warn, the consequences will not be theoretical: more measles in schools, more meningitis in college dorms, and more young adults dying of cancers that HPV shots could have prevented.

    In their view, the real danger isn’t the trace amounts of a metal that children already encounter every day. It’s rolling back the protection aluminum-adjuvanted vaccines have provided for generations.

    That’s the trade-off Offit hopes parents will see. “A choice not to get a vaccine is not a risk-free choice,” he said. “It’s just a choice to take a different risk.”

    KFF Health News is a national newsroom that produces in-depth journalism about health issues and is one of the core operating programs at KFF — the independent source for health policy research, polling, and journalism.

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  • CDC website is changed to include false claim about autism and vaccines

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    A page of the Centers for Disease Control and Prevention’s website was changed to include a false claim about autism and vaccines. Multiple CDC officials familiar with the situation said the change was made by political appointees inside the Department of Health and Human Services without input from relevant agency staffers. 

    The page about vaccines and autism formerly said that “no links have been found between any vaccine ingredients and Autism spectrum disorder.” The website has now been changed to say, “‘Vaccines do not cause autism’ is not an evidence-based claim” — a statement the Autism Science Foundation calls “misinformation” that “actually contradicts the best available science.” The CDC page also falsely claims that studies supporting a link between vaccines and autism have “been ignored by health authorities.”

    Previously, changes have only occurred in consultation with subject matter experts at the agency’s National Center on Birth Defects and Developmental Disabilities and its National Center for Immunization and Respiratory Diseases. The CDC sources told CBS News political appointees at HHS devised the change and instructed an employee inside the office of acting CDC Director Jim O’Neil to make it. 

    Autism is a developmental disability caused by differences in the brain. It presents with a wide range of symptoms that can include delays in language, learning, and social or emotional skills. The National Institutes of Health has committed hundreds of millions of dollars a year to studying the condition and trying to understand how and why it develops.

    The debunked theory that the measles, mumps and rubella vaccine causes autism has its roots in a 1998 study that was found to be fraudulent and has been retracted. Since then, “independent researchers across seven countries have conducted more than 40 high-quality studies involving over 5.6 million people,” said American Academy of Pediatrics president Susan Kressly in a statement decrying the website change. 

    “We are at a very dangerous moment for the health of America’s children,” said Dr. Sean O’Leary, chair of the AAP’s Committee on Infectious Diseases, in a news briefing on Thursday.  

    Research has found no evidence of increased rates of autism among those who are vaccinated compared to those who are not. Vaccines also undergo intensive safety testing. Research shows that genetics play a role in autism diagnoses. The NIH says some possible risk factors for autism include prenatal exposure to pesticides or air pollution, extreme prematurity or low birth weight, certain maternal health conditions, or parents conceiving at an older age.  

    “There is overwhelming evidence that vaccines do not cause autism,” said Dr. Mandy Cohen, a former CDC director. “This change to CDC language undermines the agency’s scientific integrity, damaging its credibility on vaccines and other health recommendations. Most concerning, it risks endangering children by driving down vaccination rates and leaving kids vulnerable to preventable diseases like measles and whooping cough.”

    In a statement, HHS communications director Andrew Nixon said, “This is a common-sense update that brings CDC’s website in line with our commitment to transparency and gold standard science.

    “As the updated page explains, the claim that ‘vaccines do not cause autism’ is not supported by comprehensive evidence, as studies to date have not definitively ruled out potential associations. Some research suggesting possible biologic mechanisms has been ignored or dismissed by public health agencies, and HHS is committed to finding a definitive answer,” Nixon said.

    Leading autism advocacy groups dispute that. 

    The Autism Science Foundation said in a statement it was “appalled” by the change to the CDC’s website, and highlighted the decades of research into the topic. Alison Singer, the co-founder and president of the ASF, said that while researchers “can’t do a scientific study to show that something does not cause something else,” there are a “mountain of studies that we have exonerating vaccines as a cause of autism.”

    “I think the question of whether vaccines causes autism is one that science can answer, and science has answered it,” Singer said in Thursday’s news briefing.

    A subhead saying that “Vaccines do not cause autism” remains on the CDC website with an asterisk next to it. The bottom of the page explains that the header remains in place because of an agreement with Louisiana Republican Sen. Bill Cassidy, a physician who is the chair of the Senate Health, Education, Labor, and Pensions Committee and backed HHS Robert F. Kennedy Jr. during his confirmation hearings. Cassidy said Sunday on “Face the Nation with Margaret Brennan” that he supported Kennedy in part because of “serious commitments” from the Trump administration, but did not specify what those were. 

    “I’m a doctor who has seen people die from vaccine-preventable diseases,” Cassidy wrote on social media on Thursday afternoon. “What parents need to hear right now is vaccines for measles, polio, hepatitis B and other childhood diseases are safe and effective and will not cause autism. Any statement to the contrary is wrong, irresponsible, and actively makes Americans sicker.” 

    Cassidy highlighted recent outbreaks of whooping cough and measles. He also called for more research into “the real causes of autism,” and criticized HHS funding cuts. 

    “Redirecting attention to factors we definitely know DO NOT cause autism denies families the answers they deserve,” Cassidy wrote.

    Other health agency pages with information about autism and vaccines had not been changed as of early Thursday afternoon.

    Health and Human Services Secretary Robert F. Kennedy Jr. 

    CBS News


    Kennedy has previously pushed the discredited claim that routine childhood shots cause autism. President Trump has also falsely suggested vaccines could be to blame for autism rates. Both expressed concern about rising rates of autism diagnoses, which appear to be driven by a variety of factors including increased awareness and changes in how the condition is diagnosed. 

    O’Leary said he feared the website changes would “scare parents and further stigmatize” people with autism. 

    “We have been dealing with these falsehoods for many years. They are not new. We have been promoting the science, and we’re going to continue to do that, as are the other professional societies,” he said. “The problem is now it’s coming from, these falsehoods are coming for our federal government.” 

    Experts have previously raised concerns about Kennedy reviving debunked theories about the cause of autism. In April, Kennedy announced the CDC would conduct a “massive testing and research effort” to find out what causes the disorder, and hired David Geier, a man who repeatedly claimed a link between vaccines and autism, to lead the effort. Kennedy said the work would be completed by September, though other health officials later pushed the timeline

    Dr. Fiona Havers, an infectious disease physician and former CDC official, said that the website change showed scientists “who in the past carefully vetted scientific information have been pushed aside.” 

    The “CDC should be a data-driven agency based on science and not ideology, but when you take the scientists out of the process you get rhetoric that can harm families,” said former CDC chief science and medical officer Dr. Debra Houry, who lresigned from the agency earlier this year.

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  • Minnesota’s transgender athlete policy violates Title IX, federal investigation claims

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    Federal officials say that the Minnesota Department of Education and the Minnesota State High School League both violated Title IX with their policy on transgender athletes, in a Tuesday announcement.

    The U.S. Department of Education’s Office for Civil Rights and the U.S. Department of Health and Human Services determined in a joint finding that Minnesota “allowed male athletes to compete” on several girls’ sports teams.

    MDE told WCCO it is “reviewing the letter and remains committed to ensuring every child has the opportunity to thrive in a safe and supportive school community.”

    WCCO also reached out to MSHSL for comment and is waiting for a response.

    The departments issued a proposed resolution agreement to MSHSL and the MDE, ordering them to voluntarily resolve the Title IX violation within 10 days or “risk imminent enforcement action.”

    The agreement requires the two agencies to revise any guidance “permitting males to compete in girls’ sports” to comply with Title IX and submit updated Title IX training, procedure and process materials.

    Under the agreement, MDE must also issue a statewide notice “to all federally funded entities operating interscholastic athletic programs mandating their strict compliance with Title IX by separating athletics and intimate facilities based on sex,” and the notice must require “entities to adopt biology-based definitions of ‘male’ and ‘female’” and have a reminder that non-compliance could place federal funds in jeopardy, according to a press release from HHS.

    Additionally, MDE is ordered to “restore to female athletes all records and titles misappropriated by male athletes competing in female categories,” and to send each athlete an apology letter “for allowing her educational experience to be marred by sex discrimination.” The department must also demand in writing that MSHSL take parallel action.

    Hundreds of millions of dollars in federal funding for public schools in Minnesota, which lawmakers defined as a trans refuge state in 2023, are at stake.

    The investigation began in February when MSHSL announced it would not be following an executive order signed by President Trump banning transgender girls and women from competing on sports teams that match their gender identity. Schools that don’t comply with the order risk losing federal funding and could face legal action.

    The U.S. Department of Education elevated the investigation in June and HHS initiated a compliance review around the same time. Officials specifically cited the state champion Champlin Park High School softball team, which was also the subject of another lawsuit because of a transgender pitcher.

    In April, Minnesota Attorney General Keith Ellison announced a lawsuit against the Trump administration, claiming the president’s two executive orders targeting transgender youth and adults violate both the U.S. Constitution and Title IX. The lawsuit requests the court declare the orders unconstitutional and unlawful, Ellison said. U.S. Attorney General Pam Bondi filed a motion to dismiss the lawsuit in June for lack of jurisdiction and failure to state a claim. A judge heard arguments on the motion earlier this month and has yet to make a decision.

    contributed to this report.

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  • What the research says about Tylenol and autism

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    Health Secretary Robert F. Kennedy Jr. plans to announce that the use of Tylenol by pregnant women may be linked to autism in children, according to a report Friday in the Wall Street Journal — which the Department of Health and Human Services said was “speculation.” 

    This comes after Kennedy said in April that HHS would undertake a “massive testing and research effort” to determine the cause of autism. Kennedy at the time said the plan was to release a comprehensive report in September. However, National Institutes of Health Director Dr. Jay Bhattacharya said later that month the findings could take up to a year.

    Kennedy has in the past made the unfounded claim that autism is a “preventable disease,” drawing heavy criticism from many medical experts.

    How did Tylenol maker Kenvue and HHS respond to the WSJ report?

    In a statement provided to CBS News on Friday, an HHS spokesperson called the Journal’s report “speculation.”

    “We are using gold-standard science to get to the bottom of America’s unprecedented rise in autism rates. Until we release the final report, any claims about its contents are nothing more than speculation,” the spokesperson said.

    In a separate statement in response to the WSJ story, Kenvue, the maker of Tylenol — whose active ingredient is acetaminophen — said that “we have continuously evaluated the science and continue to believe there is no causal link between acetaminophen use during pregnancy and autism. To date, the U.S. Food and Drug Administration (FDA) and leading medical organizations agree on the safety of acetaminophen, its use during pregnancy, and the information provided on the label.”

    Later Friday, Kenvue said in another statement that “we appreciate the Secretary acknowledging media coverage on the upcoming HHS report is ‘nothing more than speculation.’” 

    What do medical experts say?

    The American College of Obstetricians and Gynecologists said in a statement provided to CBS News on Friday that “there is no clear evidence that proves a direct relationship between the prudent use of acetaminophen during pregnancy and fetal developmental issues.” 

    “Neurodevelopmental disorders, in particular, are multifactorial and very difficult to associate with a singular cause,” ACOG said. “Pregnant patients should not be frightened away from the many benefits of acetaminophen, which is safe and one of the few options pregnant people have for pain relief.”

    CBS News chief medical correspondent Dr. Jon LaPook said he is looking forward to reading the upcoming report pledged by Kennedy, “especially the evidence behind any conclusions and recommendations.”

    “I spoke this afternoon to a researcher who was part of a major study published just last year that followed 2.5 million children in Sweden over 25 years,” LaPook said. “He said use of acetaminophen … was not associated with an increased risk of autism in children.” 

    Autism has become more prevalent in children born in the U.S. over the past 25 years, according to statistics compiled by the U.S. Centers for Disease Control and Prevention. But there is no scientific consensus on the reasons why.  

    In an interview with CBS News on Friday, Dr. Christine Ladd-Acosta, an associate professor of epidemiology at the Johns Hopkins Bloomberg School of Public Health and the vice director for the Wendy Klag Center for Autism and Developmental Disabilities, said research shows that the causes of autism “are complex.”

    “There have been a few dozen studies looking at Tylenol and whether use during pregnancy is associated with risk of autism in those women’s children, and the evidence has been really kind of conflicting,” Ladd-Acosta said. “Some studies have shown no association. Some have shown a positive association. Some have shown negative associations. And I think part of that is because it’s really hard to tease apart … whether it’s the medication itself that is influencing autism risk in the child, or if it has to do with the condition … the mother is using the medicine to treat that is the thing that is important in autism risk.” 

    Ladd-Acosta noted that the dosage, the length of time that pregnant women take Tylenol, and the “specific condition” they are taking it for are all factors that have been considered when attempting to determine if there is a potential association between the medication and autism.

    “There have been some associations, but there has been no conclusive evidence I’ve seen to show that Tylenol itself causes autism definitively,” Ladd-Acosta said. 

    contributed to this report.

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  • Eye Opener: RFK Jr. grilled by senators in hearing

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    Senators grill HHS Secretary Robert F. Kennedy Jr. over his policies on vaccinations. Meanwhile, conservative Supreme Court Justice Amy Coney Barrett speaks exclusively to Norah O’Donnell. More of the interview with the Justice will air on “CBS Sunday Morning” and “CBS Mornings” next week. All that and all that matters in today’s Eye Opener.

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  • Watch Live: RFK Jr. testifies at Senate hearing today amid backlash over CDC turmoil, vaccine policies

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    Sen. Ron Wyden laid into Kennedy in his opening statement, saying the secretary was responsible for fueling “mistrust” in the U.S. health care system.

    “Families are confused,” Wyden said. “They’re scared about who to trust about their health care. Robert Kennedy and Donald Trump have done so much to feed that mistrust.”

    Wyden specifically went after Kennedy for his dismantling of the vaccine structure, claiming Kennedy’s family and allies stand to potentially make financial gains from his decisions. Wyden said it’s “been obvious from the start that Robert Kennedy’s primary interest is to take vaccines away from Americans,” Wyden said. 

    “His agenda has not been about choices and information for families,” Wyden said. “Just last week, he threatened doctors that deviated from the new anti-science vaccines guidelines he released that make it harder for pregnant women and children to get the COVID vaccine.” 

    “Every single day, there has been an action that endangers the health and wellness of American families,” Wyden said. “Robert Kennedy has elevated conspiracy theorists, crackpots and grifters to make life-or-death decisions about the health care of the American people.”

    Wyden said he doesn’t think Kennedy “should be within a million miles of this job.”

    “It is in the country’s best interest that Robert Kennedy step down, and if he doesn’t, Donald Trump should fire him before more people are hurt by his reckless disregard for science and the truth,” Wyden said. 

    Wyden asked the committee to formally swear in Kennedy as a witness “given the unprecedented nature of the witness’s behavior,” but Crapo objected, saying “we will let the secretary make his own case in his opening statement.”
    “This committee’s unwillingness to swear this witness is basically a message that it is acceptable to lie to the Senate Finance Committee about hugely important questions like vaccines,” Wyden said.

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  • Over 1,000 HHS staffers call on Trump to fire RFK Jr. for “endangering the nation’s health”

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    More than 1,000 current and former Health and Human Services employees penned an open letter Wednesday calling for HHS Secretary Robert F. Kennedy Jr. to either resign or be fired.

    The letter — whose signatories were not publicly named — was released at a tense time for the health agency. Last week, Centers for Disease Control and Prevention Director Susan Monarez was fired, and several other top CDC officials resigned from their jobs in protest. Staff are also reeling from layoffs, changes to the vaccine approval system — led by Kennedy, a longtime vaccine skeptic — and a shooting outside the CDC headquarters last month.

    Wednesday’s letter accused Kennedy of “endangering the nation’s health.” It cited last week’s upheaval at the CDC, the Food and Drug Administration’s decision to rescind emergency approvals that made the COVID-19 vaccines available for young children, and the elevation of “political ideologues who pose as scientific experts” to key vaccine approval posts.

    It called for Kennedy to resign, and said that if he declines to leave his post voluntarily, President Trump should pick a new HHS secretary.

    “We swore an oath to support and defend the United States Constitution and to serve the American people. Our oath requires us to speak out when the Constitution is violated and the American people are put at risk,” the letter read.

    The letter was released by a group called Save HHS, which penned a similar open letter last month urging Kennedy to “stop spreading inaccurate health information.”

    The group said the signatories for Wednesday’s letter were provided to members of Congress, but weren’t publicly listed due to security and privacy concerns.

    HHS Communications Director Andrew Nixon responded to the letter by defending Kennedy’s record and arguing he is working to restore trust in a “broken” CDC.

    “From his first day in office, he pledged to check his assumptions at the door — and he asked every HHS colleague to do the same,” Nixon said. “That commitment to evidence-based science is why, in just seven months, he and the HHS team have accomplished more than any health secretary in history in the fight to end the chronic disease epidemic and Make America Healthy Again.”

    Separately, nine former CDC directors wrote a New York Times op-ed on Monday that castigated Kennedy for making decisions they said were “unlike anything we had ever seen at the agency,” and argued Monarez’s firing “adds considerable fuel to this raging fire.”

    Kennedy is set to testify before the Senate Finance Committee on Thursday morning, where he’s likely to face questions about the tumult at HHS.

    Last week, the White House confirmed that Monarez was fired. Her lawyers called the firing “legally deficient” and said she was “targeted” because she “refused to rubber-stamp unscientific, reckless directives and fire dedicated public health experts.”

    At least four other senior CDC leaders also stepped down last week, in some cases penning resignation letters that decried cuts to the CDC, accused the Trump administration of an “ongoing weaponizing of public health” and blasted “misinformation” about vaccines.

    Republican Sen. Bill Cassidy of Louisiana, a physician who chairs the Senate health committee, said the resignations will “require oversight.” He also sits on the Senate Finance Committee.

    Meanwhile, Kennedy ousted every member of a CDC panel responsible for making vaccine recommendations earlier this year, in some cases replacing them with people who have questioned the safety of vaccines. 

    And last week, the FDA only authorized a set of updated COVID-19 vaccines for younger adults and children with preexisting health conditions, in addition to all seniors.

    contributed to this report.

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  • Senior CDC officials resign after Monarez ouster, cite concerns over scientific independence

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    Four senior officials with the U.S. Centers for Disease Control and Prevention announced their resignations in recent days, citing what they described as growing political interference in the agency’s scientific work, particularly regarding vaccines.

    Two of those — Dr. Debra Houry, the CDC’s Chief Science and Medical Officer, and Dr. Demetre Daskalakis, who led the National Center for Immunization and Respiratory Diseases — stepped down on Wednesday, hours after the White House announced the firing of CDC Director Susan Monarez.

    Monarez, confirmed by the Senate in late July, was removed less than a month into her tenure. White House spokesman Kush Desai said Monarez “was not aligned with the President’s agenda of Making America Healthy Again.” Monarez’s attorneys argue the dismissal is unlawful, asserting that only the president can remove a Senate-confirmed director.

    On Thursday, deputy secretary of Health and Human Services Jim O’Neill was chosen to serve as acting CDC director, several White House officials confirmed to CBS News. And in an internal email sent to CDC staff Thursday evening, Secretary of Health and Human Services Robert F. Kennedy Jr. confirmed O’Neill as the acting CDC director, but did not address Monarez’s departure.  

    I am committed to working with you to restore trust, transparency, and credibility to the CDC,” Kennedy told CDC employees, later writing that “President Trump and I are aligned on the commonsense vision for the CDC: Strengthen the public health infrastructure by returning to its core mission of protecting Americans from communicable diseases by investing in innovation to prevent, detect and respond to future threats.”

    Houry and Daskalakis said they had become increasingly uneasy about how vaccine policy was being handled. Both pointed to preparations for the Advisory Committee on Immunization Practices meeting, which recommends vaccine schedules.

    Houry said they feared “some decisions had been made before there was even the data or the science to support those. We are scientists, and that was concerning to us.”

    Daskalakis added that he was “very concerned that there’s going to be an attempt to re-litigate vaccines that have already had clear recommendations with science that has been vetted,” which he warned could undermine public trust. “If you can’t attack access, then why not attack trust? And that’s what I think the playbook is,” he said.

    Both officials cited instances in which evidence reviews were altered or withdrawn. A CDC analysis of thimerosal, a vaccine preservative, was briefly posted before being taken down at HHS’s direction. “If there’s something that doesn’t line up with the recommendations, then that information will be taken down, and it’s not there for the public to see for openness and transparency,” Houry said.

    The two also criticized what they described as a lack of direct communication between CDC scientists and HHS leadership. Daskalakis said his team was never invited to brief Kennedy on topics ranging from measles to COVID.

    When asked about Kennedy’s calls for “radical transparency,” Houry and Daskalakis described learning about changes to the COVID vaccine schedule for children not through internal channels but via social media.

    “The radical transparency manifested itself by a Twitter post, which is how Dr. Houry and I learned that the secretary had mandated the change in the children’s vaccine schedule for COVID,” Daskalakis recalled. “What is the background that led to that decision? And we were denied access to that information. So, I don’t think that that’s radically transparent,” Daskalakis said.

    CBS News reached out to HHS for comment on some of the allegations made by Houry and Daskalakis, but did not immediately hear back. 

    Both officials said they had no jobs lined up when they resigned. Houry described the decision as an effort to raise the alarm about the direction of the agency.

    “For us, this was really sending out a bat signal,” Houry said. “We were the very senior scientists and career leaders at CDC. We thought this was the time to stand together and try to do what we could to raise the alarm around public health in our country.”

    Daskalakis said remaining at CDC under current conditions would have made them complicit in what he called the “weaponization” of public health. 

    “The safety has already been compromised…We are flying blind in the U.S. already. If we continued…we would be complicit and would be facilitating the ability to go from flying blind to actively harming people,” he said.

    Houry emphasized the severity of the moment by noting that she left without a backup plan. 

    “My leaving without a job was really just showing how dire the circumstances had become,” Houry said. 

    Daskalakis said his decision was also shaped by his medical oath. 

    “As a physician, I take the Hippocratic oath: first, do no harm. I am seeing ideology permeating science in a way that is going to harm children and adults…I think we are seeing things that are happening that are making our country less prepared to be able to respond to the everyday pathogens …but also … to the next big thing.”

    Both also expressed concerns for their personal safety in the current climate. 

    “The environment we live in… stoked by misinformation, especially from people considered by some to be health authorities, makes me worried for all of us in public health,” Daskalakis said. “I am concerned, but that’s part of our job…to be brave and continue to speak the truth even when we are outside of the CDC.”

    The resignations came weeks after a shooting outside the CDC’s Atlanta headquarters, which law enforcement linked to COVID misinformation.

    Houry said the White House response to the shooting was muted. Kennedy toured the site but later gave an interview expressing distrust of experts. “That was after the attack. It was based on COVID misinformation. So this is when we were trying to build trust,” she said.

    Daskalakis added that while Kennedy later described mass shootings as a public health crisis, he believed the secretary should address misinformation as a root cause. “The misinformation about the COVID vaccine that has been documented by the Georgia bureau of investigation as the reason for the shooter at CDC. I would really recommend that the secretary actually do take his own advice and actually address the core problem that led to that shooting as well,” he said. He also noted that CDC’s own gun violence prevention programs had been sharply reduced. “We talk about violence as a public health problem. It is, and there’s things we can do to prevent it. Unfortunately, the majority of that program, the staff are terminated.”

    The firings and resignations have sparked calls for oversight. Independent Sen. Bernie Sanders of Vermont called for a bipartisan investigation, Democratic Sen. Patty Murray of Washington urged Kennedy’s removal, and Republican Sen. Bill Cassidy of Louisiana — who voted to confirm Kennedy’s appointment as HHC secretary — said the developments would “require oversight.”

    The events come as the Food and Drug Administration narrowed eligibility for updated COVID-19 vaccines to older adults and people with risk factors for severe COVID.

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  • Billions in NIH grants could be jeopardized by appointments snafu, Republicans say

    Billions in NIH grants could be jeopardized by appointments snafu, Republicans say

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    The Biden administration allegedly failed to correctly reappoint more than a dozen top-ranking National Institutes of Health leaders, House Republicans say, raising questions about the legality of billions in federal grants doled out by those officials over the last year. 

    Their claim, detailed Friday in a letter to Health and Human Services Secretary Xavier Becerra, obtained by CBS News, follows a monthslong probe led by Rep. Cathy McMorris Rodgers, the Republican chair of the House Energy & Commerce Committee, into vacancies at the agency.

    “The failure to reappoint the above NIH IC Directors jeopardizes the legal validity of more than $25 billion in federal biomedical research grants made in 2022 alone,” the committee wrote.

    The Biden administration rebutted the GOP-led committee’s accusations that it ran afoul of the law. An HHS official familiar with the matter, who responded on the condition of anonymity, said the committee was misrepresenting the requirements.

    The committee’s letter stems from the 21st Century Cures Act passed in 2016, which says that directors atop the institutes and centers within the NIH have five-year term limits before they must be reappointed. 

    When the term limits of 14 of these officials came due at the end of 2021, the Biden administration says the NIH director correctly reappointed them. The law says that they must be “appointed by the Secretary, acting through the Director of the National Institutes of Health.”

    The committee says that the way those officials were reappointed falls short of what the law demands from Becerra himself.

    “Specifically, it requires the Secretary of HHS to reappoint NIH IC Directors, including those who were serving at the time of the law’s enactment when their five-year terms expired on December 12, 2021,” the letter stated.

    After the committee’s probe was launched, Becerra signed affidavits the department says retroactively ratified and adopted the appointments. 

    While the Biden administration thinks its grants remain on sound footing, the HHS official said Becerra’s affidavits were intended to bolster defenses against challenges that might upend them in the courts.  

    The committee questioned the legality of that move. Among the issues it flagged were the retirements of Dr. Anthony Fauci, formerly head of the National Institutes of Allergy and Infectious Diseases, and Dr. Roger Glass, who had headed the Fogarty International Center. Both stepped down months before Becerra signed the affidavits in June.

    “HHS and the NIH should have known within days of receiving the Committee’s March 14, 2022, letter that the reappointments as legally required had not occurred. Rather than addressing the problem in consultation with the Committee, HHS and the NIH repeatedly misled the Committee,” the committee wrote of its  monthslong back-and-forth with the department. 

    The HHS official insisted that the department had cooperated with the committee’s questions in good faith, voluntarily producing documents and responses to the inquiry.

    National Institutes of Health building in Bethesda, Maryland
    National Institutes of Health James Shannon building on the campus of NIH in Bethesda, Maryland.

    AP Photo/Pablo Martinez Monsivais


    Thousands of researchers compete every year for NIH funding, which support a variety of projects ranging from fundamental laboratory research to human clinical trials. 

    Asked how those programs might be affected, a committee aide told CBS News, “It is unclear what the impact will be, but it creates unnecessary uncertainty and opens the door to legal challenges, While we are unaware of any other Cabinet Secretaries committing such egregious process violations, a similar case involving SEC Administrative Law Judges required the decisions made by improperly appointed officials be relitigated in front of a legally appointed judge.”

    The committee says its probe into the issue is continuing and prompted a renewed round of questions to the department, as well as the possibility of demanding interviews from HHS and NIH officials.  

    Its letter to Becerra warned that “intentional misstatements or omissions” may constitute “federal criminal violations under 18 USC 1001,” adding that it serves as a formal request to preserve “all existing and future records.”

    “Institute directors with discretion to award billions or even hundreds of millions in research funding are, by definition, exercising significant authority pursuant to the laws of the United States. As such, institute directors are the quintessential ‘inferior officers,’” a former senior HHS official told CBS News. 

    “The Secretary cannot delegate his or her constitutional authority to appoint inferior officers. It is my understanding that prior administrations of both parties zealously guarded the appointments process and took care to ensure that inferior officers were properly appointed,” said the former senior official, who previously served in the Bush, Reagan and Trump administrations.

    Senate Health, Education, Labor and Pensions Committee
    From left: Dr. Anthony Fauci, then director of National Institute of Allergy and Infectious Diseases; Dr. Richard Hodes, director of the National Institute on Agingl and Dr. Francis Collins, then director of the National Institutes of Health, testify at a Senate committee hearing on Aug. 23, 2018.

    Tom Williams/CQ Roll Call


    The Republican-led committee’s letter comes as the Biden administration has yet to fill key vacancies in the NIH leadership. 

    The agency has been without a director since December 2021, when Dr. Francis Collins stepped down from his post. 

    In May, President Biden announced he planned to nominate Dr. Monica Bertagnolli — currently head of the NIH’s National Cancer Institute — to fill the role.

    So far, Bertagnolli’s nomination is awaiting Senate confirmation. 

    Independent Sen. Bernie Sanders, chair of the panel charged with signing off on HHS nominees, has vowed not to move forward with the nomination without new pledges from the Biden administration on drug prices. 

    “I will oppose all nominations until we have a very clear strategy on the part of the government … as to how we’re going to lower the outrageously high cost of prescription drugs,” Sanders told The Washington Post last month.

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