Abortions continued rising in 2024 despite state bans: Report
More women were able to access abortion care in 2024 than the previous year despite state bans, reflecting a continued increase in the three years since the Supreme Court overturned Roe v. Wade, according to a report issued Monday.
The latest report from the #WeCount project of the Society of Family Planning, which supports abortion access, found there were about 1.14 million abortions provided by licensed clinicians across the U.S. in 2024, compared with 1.06 million in 2023.
The report was released a day before the third anniversary of the Supreme Court's Dobbs decision ended the nearly 50-year constitutional right to an abortion. #WeCount began after Roe was overturned and has been tracking abortions since 2022.
However, the 2022 numbers don't include January through March, when abortions are traditionally at their highest.
In-person care at brick-and-mortar clinics represented the majority of abortion care, even though the number of abortions has fallen to near zero in states that enforce bans.
The number of abortions using medication prescribed and delivered through telehealth has continued to increase since April 2022 and now makes up 1 in 4 procedures. Prior to the Dobbs ruling, about 1 in 20 abortions were accessed through telehealth.
About half of the telehealth abortions last year were facilitated by the shield laws in some Democratic-controlled states. Shield laws protect medical providers and others from out-of-state investigations and prosecutions regarding abortions and gender-affirming care.
An average of 12,330 abortions per month were provided under shield laws by the end of 2024, the report found.
The report's findings show abortion bans haven't stopped people from seeking care, Alison Norris, #WeCount co-chair and professor at Ohio State University's College of Public Health, said in a statement.
'As care shifts across state lines and into telehealth care, what's emerging is a deeply fragmented system where access depends on where you live, how much money you have, and whether you can overcome barriers to care,' Norris said.
Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.
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The Hill
11 hours ago
- The Hill
Congress should look to Tennessee as an example for Medicaid reform
As Congress wrestles with the need to trim spending, attention has turned to Medicaid, and to a lesser extent, Medicare. These are hardly new issues. Within seven years of the 1965 enactment of Medicaid, for those eligible for federal income support (largely those in poverty), and Medicare, primarily for those eligible for Social Security, Congress in 1972 turned its attention to concerns about containing costs in those programs. Tennessee has been a pioneer in managing its Medicaid costs, and Congress might benefit from the Tennessee experience with TennCare, the state's Medicaid program. About 30 years ago, Tennessee faced unsustainable annual increases in its Medicaid program. A popular Democratic governor, Ned McWherter, called the state's Medicaid program the Pac Man of the state's budget. He sought to find a way to pay for the Medicaid increases through a state income tax (Tennessee does not have one) but failed. The TennCare program was designed to address the issue by containing the rate of increase in costs. Tennessee received a waiver so that it could implement a universal and mandatory managed care program. Tennessee had no managed care in Medicaid, and a move to 100 percent managed care was projected to reduce costs by 20-25 percent on a recurring basis. Support from patient advocates was secured by agreeing that cost savings would be used to increase access to Medicaid to previously uncovered persons. The mandatory Medicaid managed care program was deemed such a success that, in 1997, Congress allowed states to implement Medicaid managed care without a waiver. Managed care introduced economic considerations into the process of medical decision-making. While the cost savings projections were pretty much on target; once those savings were fully realized, the projections recognized that the rate of cost escalation would be restored, albeit from a lower cost basis. That projection also turned out to be pretty accurate. A Republican governor, Don Sundquist, succeeded McWherter and unsuccessfully sought to implement an income tax. Another wonderful Democratic governor, Phil Bredesen, was elected to succeed Sundquist under a promise not to seek an income tax. Bredesen was determined to find a way to manage down the rate of increase of Medicaid spending. I served as his outside counsel. A reform team determined that the target for reform should focus on the concept of 'medical necessity.' That insight was informed by work I had done as part of an Institute of Medicine study group, which looked at hospital staffing in a system that had recently merged three hospitals. There were three distinct models, and no consensus about which was the 'right' one. Traditionally, the concept of 'medical necessity' was the term used to define the scope of benefits under health plans, including Medicaid. The concept assumed that there was a single correct way of practicing medicine, and that it had a justification based on scientific consensus. But the existence of clinical uncertainty called into question that traditional view. As it turned out, many alternatives were available at varying costs, and evidence of superiority of one particular approach was often lacking. Those insights led to the policy conclusion that, if a more expensive alternative were proposed, the state should not pay for that more expensive alternative unless there was good scientific evidence that it was superior and worth the additional cost. If an aspirin were adequate, it should be used instead of a more expensive prescription-based alternative. If an adequate outpatient procedure were available at lower cost, TennCare should not pay for a more expensive inpatient option. These insights resulted in a TennCare definition of 'medical necessity' that could serve as a national model at considerable (but hard to measure) cost savings. That definition has been in place for nearly 20 years and has been approved by a federal court. TennCare has kept costs manageable so that the state has been able to live within existing sources of revenue, and the state even proposed to accept financial risk if it could share in the cost savings from TennCare above a projected baseline. The TennCare definition includes the traditional requirement that a medical item or service be recommended by a treating physician (no doctor shopping) and that it be 'safe and effective.' The reasonably anticipated medical benefits must 'outweigh' the reasonably anticipated medical risks 'based on the enrollee's condition and scientifically supported evidence' to be covered under TennCare. That is, a medically based risk-benefit calculation is a requirement as part of medical decision-making. The innovative aspects have three components. First, a medical item or service must be required 'in order to diagnose or treat an enrollee's medical condition.' That circumscribes the type of item or service covered under the program. Second, the medical item or service must be the 'least costly alternative course of diagnosis or treatment.' That expressly incorporates economic factors into medical decision-making. An alternative course of diagnosis or treatment 'may include observation, lifestyle or behavioral changes, or, where appropriate, no treatment at all.' If an item or service can be safely provided in an outpatient setting at lower cost, then that is what TennCare will pay for. More expensive inpatient treatment is not 'medically necessary.' Third, the less costly alternative need only be 'adequate for the medical condition of the enrollee.' The yardstick is not the best possible standard or some comparison with private plans. The standard of 'adequacy' means that sub-standard medicine is not acceptable, but that some differences between benefits for TennCare enrollees and those on private plans are acceptable. These innovations were controversial 20 years ago, when proposed and enacted, but they have become part of the fabric of TennCare and have been in place successfully for two decades. They help shape the medical decision-making culture that costs are to be considered and that the issue is the adequacy of care not what might be available in some private plans. That type of modest stratification, by the way, is expressly endorsed in the Affordable Care Act. Section 1302(b)(5) expressly allows for supplementation by health plans beyond the essential health benefits mandated by the Affordable Care Act. In the discussions that led to these reforms, the estimated range of savings was from 1 percent to 5 percent of total Medicaid spending. In an environment in which a program entails large expenditures, even a 1 percent per year savings could be considerable. James F. Blumstein is University Distinguished Professor at Vanderbilt Law School and the director of Vanderbilt's Health Policy Center.


Politico
11 hours ago
- Politico
Graham feels Tillis' pain
As Republicans in Congress look to get President Donald Trump's sweeping megabill to the Oval Office by July 4, one Democratic Senator is predicting the bill will crater support for the GOP across the country. Virginia Sen. Mark Warner told CNN's Jake Tapper on Sunday that the Medicaid cuts in Trump's 'Big Beautiful Bill' will prove especially unpopular. 'I think the overwhelming amount of data shows that on this one, this is tax cuts for the wealthiest to end up cutting health care, plain and simple,' Warner said on 'State of the Union.' 'You can put any lipstick you want on this pig, but it's still a pig.' Senate Republicans on Saturday narrowly voted to start debate on the megabill, with just two members of the caucus, Kentucky Sen. Rand Paul and North Carolina Sen. Thom Tillis, voting against moving forward. The chamber could likely pass the bill by Monday. A June estimate from the Congressional Budget Office found that the bill and other health care rules could push 16 million people off health insurance. Warner told Tapper that it would 'about double' the uninsured rate in his commonwealth of Virginia. 'The fact of the matter is, what this does baseline is all these cuts, all this cutback on health care to provide the wealthiest in our country a disproportionate share of tax cuts,' he said. 'That just doesn't seem fair. And the more we can get that out, I think this will be a political albatross.'


Atlantic
13 hours ago
- Atlantic
The Liberal Misinformation Bubble About Youth Gender Medicine
Allow children to transition, or they will kill themselves. For more than a decade, this has been the strongest argument in favor of youth gender medicine—a scenario so awful that it stifled any doubts or questions about puberty blockers and cross-sex hormones. 'We often ask parents, 'Would you rather have a dead son than a live daughter?'' Johanna Olson-Kennedy of Children's Hospital Los Angeles once explained to ABC News. Variations on the phrase crop up in innumerable media articles and public statements by influencers, activists, and LGBTQ groups. The same idea—that the choice is transition or death—appeared in the arguments made by Elizabeth Prelogar, the Biden administration's solicitor general, before the Supreme Court last year. Tennessee's law prohibiting the use of puberty blockers and cross-sex hormones to treat minors with gender dysphoria would, she said, 'increase the risk of suicide.' But there is a huge problem with this emotive formulation: It isn't true. When Justice Samuel Alito challenged the ACLU lawyer Chase Strangio on such claims during oral arguments, Strangio made a startling admission. He conceded that there is no evidence to support the idea that medical transition reduces adolescent suicide rates. At first, Strangio dodged the question, saying that research shows that blockers and hormones reduce 'depression, anxiety, and suicidality'—that is, suicidal thoughts. (Even that is debatable, according to reviews of the research literature.) But when Alito referenced a systematic review conducted for the Cass report in England, Strangio conceded the point. 'There is no evidence in some—in the studies that this treatment reduces completed suicide,' he said. 'And the reason for that is completed suicide, thankfully and admittedly, is rare, and we're talking about a very small population of individuals with studies that don't necessarily have completed suicides within them.' Here was the trans-rights movement's greatest legal brain, speaking in front of the nation's highest court. And what he was saying was that the strongest argument for a hotly debated treatment was, in fact, not supported by the evidence. Even then, his admission did not register with the liberal justices. When the court voted 6–3 to uphold the Tennessee law, Sonia Sotomayor claimed in her dissent that 'access to care can be a question of life or death.' If she meant any kind of therapeutic support, that might be defensible. But claiming that this is true of medical transition specifically—the type of care being debated in the Skrmetti case—is not supported by the current research. Advocates of the open-science movement often talk about 'zombie facts' —popular sound bites that persist in public debate, even when they have been repeatedly discredited. Many common political claims made in defense of puberty blockers and hormones for gender-dysphoric minors meet this definition. These zombie facts have been flatly contradicted not just by conservatives but also by prominent advocates and practitioners of the treatment—at least when they're speaking candidly. Many liberals are unaware of this, however, because they are stuck in media bubbles in which well-meaning commentators make confident assertions for youth gender medicine—claims from which its elite advocates have long since retreated. Perhaps the existence of this bubble shouldn't be surprising. Many of the most fervent advocates of youth transition are also on record disparaging the idea that it should be debated at all. Strangio—who works for the country's best-known free-speech organization—once tweeted that he would like to scuttle Abigail Shrier's book Irreversible Damage, a skeptical treatment of youth gender medicine. Strangio declared, 'Stopping the circulation of this book and these ideas is 100% a hill I will die on.' Marci Bowers, the former head of the World Professional Association for Transgender Health (WPATH), the most prominent organization for gender-medicine providers, has likened skepticism of child gender medicine to Holocaust denial. 'There are not two sides to this issue,' she once said, according to a recent episode of The Protocol, a New York Times podcast. Boasting about your unwillingness to listen to your opponents probably plays well in some crowds. But it left Strangio badly exposed in front of the Supreme Court, where it became clear that the conservative justices had read the most convincing critiques of hormones and blockers—and had some questions as a result. Trans-rights activists like to accuse skeptics of youth gender medicine—and publications that dare to report their views—of fomenting a ' moral panic.' But the movement has spent the past decade telling gender-nonconforming children that anyone who tries to restrict access to puberty blockers and hormones is, effectively, trying to kill them. This was false, as Strangio's answer tacitly conceded. It was also irresponsible. After England restricted the use of puberty blockers in 2020, the government asked an expert psychologist, Louis Appleby, to investigate whether the suicide rate for patients at the country's youth gender clinic rose dramatically as a result. It did not: In fact, he did not find any increase in suicides at all, despite the lurid claims made online. 'The way that this issue has been discussed on social media has been insensitive, distressing and dangerous, and goes against guidance on safe reporting of suicide,' Appleby reported. 'One risk is that young people and their families will be terrified by predictions of suicide as inevitable without puberty blockers.' When red-state bans are discussed, you will also hear liberals say that conservative fears about the medical-transition pathway are overwrought—because all children get extensive, personalized assessments before being prescribed blockers or hormones. This, too, is untrue. Although the official standards of care recommend thorough assessment over several months, many American clinics say they will prescribe blockers on a first visit. This isn't just a matter of U.S. health providers skimping on talk therapy to keep costs down; some practitioners view long evaluations as unnecessary and even patronizing. 'I don't send someone to a therapist when I'm going to start them on insulin,' Olson-Kennedy told The Atlantic in 2018. Her published research shows that she has referred girls as young as 13 for double mastectomies. And what if these children later regret their decision? 'Adolescents actually have the capacity to make a reasoned logical decision,' she once told an industry seminar, adding: 'If you want breasts at a later point in your life, you can go and get them.' Perhaps the greatest piece of misinformation believed by liberals, however, is that the American standards of care in this area are strongly evidence-based. In fact, at this point, the fairest thing to say about the evidence surrounding medical transition for adolescents—the so-called Dutch protocol, as opposed to talk therapy and other support—is that it is weak and inconclusive. (A further complication is that American child gender medicine has deviated significantly from this original protocol, in terms of length of assessments and the number and demographics of minors being treated.) Yes, as activists are keen to point out, most major American medical associations support the Dutch protocol. But consensus is not the same as evidence. And that consensus is politically influenced. Rachel Levine, President Joe Biden's assistant secretary for health and human services, successfully lobbied to have age minimums removed for most surgeries from the standards of care drawn up by WPATH. That was a deeply political decision—Levine, according to emails from her office reviewed by the Times, believed that listing any specific limits under age 18 would give opponents of youth transition hard targets to exploit. More recently, another court case over banning blockers and hormones, this time in Alabama, has revealed that WPATH members themselves had doubts about their own guidelines. In 2022, Alabama passed a law criminalizing the prescription of hormones and blockers to patients under 19. After the Biden administration sued to block the law, the state's Republican attorney general subpoenaed documents showing that WPATH has known for some time that the evidence base for adolescent transition is thin. 'All of us are painfully aware that there are many gaps in research to back up our recommendations,' Eli Coleman, the psychologist who chaired the team revising the standards of care, wrote to his colleagues in 2023. Yet the organization did not make this clear in public. Laura Edwards-Leeper—who helped bring the Dutch protocol to the U.S. but has since criticized in a Washington Post op-ed the unquestioningly gender-affirmative model—has said that the specter of red-state bans made her and her op-ed co-author reluctant to break ranks. The Alabama litigation also confirmed that WPATH had commissioned systematic reviews of the evidence for the Dutch protocol. However, close to publication, the Johns Hopkins University researcher involved was told that her findings needed to be 'scrutinized and reviewed to ensure that publication does not negatively affect the provision of transgender health care.' This is not how evidence-based medicine is supposed to work. You don't start with a treatment and then ensure that only studies that support that treatment are published. In a legal filing in the Alabama case, Coleman insisted 'it is not true' that the WPATH guidelines 'turned on any ideological or political considerations' and that the group's dispute with the Johns Hopkins researcher concerned only the timing of publication. Yet the Times has reported that at least one manuscript she sought to publish 'never saw the light of day.' The Alabama disclosures are not the only example of this reluctance to acknowledge contrary evidence. Last year, Olson-Kennedy said that she had not published her own broad study on mental-health outcomes for youth with gender dysphoria, because she worried about its results being 'weaponized.' That raised suspicions that she had found only sketchy evidence to support the treatments that she has been prescribing—and publicly advocating for—over many years. Last month, her study finally appeared as a preprint, a form of scientific publication where the evidence has not yet been peer-reviewed or finalized. Its participants 'demonstrated no significant changes in reported anxious/depressed, withdrawn/depressed, somatic complaints, social problems, thought problems, attention problems, aggressive behavior, internalizing problems or externalizing problems' in the two years after starting puberty blockers. (I have requested comment from Olson-Kennedy via Children's Hospital Los Angeles but have not yet heard back.) The reliance on elite consensus over evidence helps make sense of WPATH's flatly hostile response to the Cass report in England, which commissioned systematic reviews and recommended extreme caution over the use of blockers and hormones. The review was a direct challenge to WPATH's ability to position itself as the final arbiter of these treatments—something that became more obvious when the conservative justices referenced the British document in their questions and opinions in Skrmetti. One of WPATH's main charges against Hilary Cass, the senior pediatrician who led the review, was that she was not a gender specialist—in other words, that she was not part of the charmed circle who already agreed that these treatments were beneficial. Because of WPATH's hostility, many on the American left now believe that the Cass review has been discredited. 'Upon first reading, especially to a person with limited knowledge of the history of transgender health care, much of the report might seem reasonable,' Lydia Polgreen wrote in the Times last August. However, after 'poring over the document' and 'interviewing experts in gender-affirming care,' Polgreen realized that the Cass review was 'fundamentally a subjective, political document.' Advocates of youth gender medicine have reacted furiously to articles in the Times and elsewhere that take Cass's conclusions seriously. Indeed, some people inside the information bubble appear to believe that if respectable publications would stop writing about this story, all the doubts and questions—and Republican attempts to capitalize on them electorally—would simply disappear. Whenever the Times has published a less-than-cheerleading article about youth transition, supporters of gender medicine have accused the newspaper of manufacturing a debate that otherwise would not exist. After the Skrmetti decision, Strangio was still describing media coverage of the issue as 'insidious,' adding: ' The New York Times, especially, has been fixated on casting the medical care as being of an insufficient quality.' Can this misinformation bubble ever be burst? On the left, support for youth transition has been rolled together with other issues—such as police reform and climate activism—as a kind of super-saver combo deal of correct opinions. The 33-year-old democratic socialist Zohran Mamdani has made funding gender transition, including for minors, part of his pitch to be New York's mayor. But complicated issues deserve to be treated individually: You can criticize Israel, object to the militarization of America's police forces, and believe that climate change is real, and yet still not support irreversible, experimental, and unproven medical treatments for children. The polarization of this issue in America has been deeply unhelpful for getting liberals to accept the sketchiness of the evidence base. When Vice President J. D. Vance wanted to troll the left, he joined Bluesky—where skeptics of youth gender medicine are among the most blocked users—and immediately started talking about the Skrmetti judgment. Actions like that turn accepting the evidence base into a humiliating climbdown. Acknowledging the evidence does not mean that you also have to support banning these treatments—or reject the idea that some people will be happier if they transition. Cass believes that some youngsters may indeed benefit from the medical pathway. 'Whilst some young people may feel an urgency to transition, young adults looking back at their younger selves would often advise slowing down,' her report concludes. 'For some, the best outcome will be transition, whereas others may resolve their distress in other ways.' I have always argued against straightforward bans on medical transition for adolescents. In practice, the way these have been enacted in red states has been uncaring and punitive. Parents are threatened with child-abuse investigations for pursuing treatments that medical professionals have assured them are safe. Children with severe mental-health troubles suddenly lose therapeutic support. Clinics nationwide, including Olson-Kennedy's, are now abruptly closing because of the political atmosphere. Writing about the subject in 2023, I argued that the only way out of the culture war was for the American medical associations to commission reviews and carefully consider the evidence. From the July/August 2018 issue: When children say they're trans However, the revelations from Skrmetti and the Alabama case have made me more sympathetic to commentators such as Leor Sapir, of the conservative Manhattan Institute, who supports the bans because American medicine cannot be trusted to police itself. 'Are these bans the perfect solution? Probably not,' he told me in 2023. 'But at the end of the day, if it's between banning gender-affirming care and leaving it unregulated, I think we can minimize the amount of harm by banning it.' Once you know that WPATH wanted to publish a review only if it came to the group's preferred conclusion, Sapir's case becomes more compelling. Despite the concerted efforts to suppress the evidence, however, the picture on youth gender medicine has become clearer over the past decade. It's no humiliation to update our beliefs as a result: I regularly used to write that medical transition was 'lifesaving,' before I saw how limited the evidence on suicide was. And it took another court case, brought by the British detransitioner Keira Bell, for me to realize fully that puberty blockers were not what they were sold as—a 'safe and reversible' treatment that gave patients 'time to think' —but instead a one-way ticket to full transition, with physical changes that cannot be undone. Some advocates for the Dutch protocol, as it's applied in the United States, have staked their entire career and reputation on its safety and effectiveness. They have strong incentives not to concede the weakness of the evidence. In 2023, the advocacy group GLAAD drove a truck around the offices of The New York Times to declare that the ' science is settled.' Doctors such as Olson-Kennedy and activists such as Strangio are unlikely to revise their opinions. For everyone else, however, the choice is still open. We can support civil-rights protections for transgender people without having to endorse an experimental and unproven set of medical treatments—or having to repeat emotionally manipulative and now discredited claims about suicide. I am not a fan of the American way of settling political disputes, by kicking them over to an escalating series of judges. But in the case of youth gender medicine, the legal system has provided clarity and disclosure that might otherwise not exist. Thanks to the Supreme Court's oral questioning in Skrmetti and the discovery process in Alabama, we now have a clearer picture of how youth gender medicine has really been operating in the United States, and an uncomfortable insight into how advocacy groups and medical associations have tamped down their own concerns about its evidence base. Those of us who have been urging caution now know that many of our ostensible opponents had the same concerns. They just smothered them, for political reasons.