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    Biden administration seeks to expand health coverage to Dreamers

    The Biden administration is seeking to allow immigrants known as Dreamers, who were brought to the US as children by undocumented parents, greater access to health insurance through federal programs, the White House said on Thursday.The proposal would allow participants in the Deferred Action for Childhood Arrivals program, or Daca, to access to health insurance under Medicaid and Affordable Care Act (ACA) exchanges, it said.“Healthcare should be a right. I’ve worked hard to get more Americans health insurance than ever before,” Joe Biden said on Twitter, adding the move would give “Dreamers the same opportunities.”The proposed rule comes as efforts to further protect Dreamers stalls in Congress and faces legal challenges. About 580,000 people were enrolled as of last year in the Obama-era 2012 Daca program, which grants protection from deportation and work permits.An expansion would allow Daca recipients to enroll in coverage under the joint federal-state Medicaid program or through private insurers participating in the exchanges established by the 2010 ACA law also passed under Democratic then President Barack Obama and Biden, his vice-president.Eight US states have already expanded state insurance access to health coverage regardless of immigration status, according to data from the healthcare policy organization Kaiser Family Foundation.Biden promised during his 2020 presidential campaign to protect “Dreamers” and their families after Republican then President Donald Trump tried to end Daca. Biden this week said he plans to seek a second four-year term but has not formally announced his re-election bid.The president, in a video, reiterated his call for Congress to establish a pathway to citizenship for Daca recipients, adding: “While we work toward that goal … we need to give Dreamers the opportunities and the support they deserve.”One source familiar with the plan said it could take months or longer to finalize through the federal regulatory process.Democratic representative Pramila Jayapal, chair of the congressional progressive caucus, which last month urged the administration to expand access, called the move “a long overdue step toward immigrant justice”.Republicans, however, have cast doubt on Daca and other immigration reforms.Texas and other US states with Republican attorneys general are challenging the program in court. More

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    To protect abortion access, the FDA should decline to enforce a mifepristone ban | David S Cohen, Greer Donley and Rachel Rebouché

    On Friday, the nation faced dueling decisions from federal judges regarding the first drug in a medication abortion: mifepristone. A judge in Texas ruled that the Food and Drug Administration (FDA) likely improperly approved the drug, putting mifepristone’s approval on hold while the case plays out (though this order won’t take effect until late Friday this week). Minutes later, a judge in Washington state ruled that the FDA could not change the status quo regarding mifepristone’s availability.In response to these two cases and two other less-publicized cases involving the FDA and medication abortion, the agency needs to chart a course consistent with its mission to protect patient health and to follow the evidence. As the Biden administration has stated, protecting medication abortion is a public health imperative now that states can ban all abortion outright. If the agency does not respond to these conflicting rulings in a manner tailored to provide the greatest access possible to medication abortion, it will be telling of Biden’s commitment to reproductive justice.Though the case in Texas has garnered enormous attention, it is not the only case thrusting the FDA into the center of the abortion debate. The others have the opposite goal of improving access to the drug. The litigation in Washington state, not widely discussed until Friday, centered around the FDA’s special and onerous regulation of medication abortion. Eighteen state attorneys general sued the FDA arguing that the agency’s overregulation is not justified by the statute or the drug’s safety and must be lifted. If successful on appeal, this would ensure mifepristone is treated like other prescription drugs – prescribed through any provider and accessible at any pharmacy.Plaintiffs in two other cases are pushing even further, trying to use the FDA’s special regulation of mifepristone to argue that a state cannot ban or overregulate the drug. These lawsuits, filed respectively by the generic manufacturer of mifepristone in West Virginia and a physician in North Carolina, might restore access to medication abortion across the country. The plaintiffs argue that federal approval of mifepristone trumps state abortion laws, essentially forcing all states to allow medication abortion as regulated by the FDA.The FDA is caught in the crosshairs. Though the agency prides itself on scientific independence and seeks to avoid the appearance of partisanship, any reaction the agency has to these cases – even a decision not to act – will appear political to one side. Nonetheless, the FDA must push forward to ensure access to this critical drug.Starting with the two cases just decided, the agency can comply with both by announcing that it will exercise enforcement discretion. Enforcement discretion allows the agency to provide safe harbor for technical violations of law. So even if mifepristone becomes an unapproved drug per the Texas order, the agency could announce that it would not pursue action against the entities that market or dispense the drug to maintain the status quo as required by the Washington case.This would not require the agency to “ignore” the Texas order, as some have suggested. Rather, enforcement discretion is a normal part of the FDA’s operation and only relevant if the drug becomes unapproved as ordered. The FDA could exercise this discretion without being ordered to by the Washington court, but the Washington case provides enormous political cover for the agency to use this discretion.Repercussions for patient and public health could result from the FDA failing to clearly exercise its enforcement discretion. Clinicians may turn to a different medication abortion regimen that does not include mifepristone and is outside of current FDA regulation. Though alternative regimens will be vital to maintaining abortion access if mifepristone becomes inaccessible, they are slightly less effective and, more importantly, will upend what has been the uniform, established protocol for a medication abortion in the United States for over two decades. Relatedly, confusion is sure to reign after the Texas decision unless the FDA speaks in a clear and timely voice. Already, certain abortion providers have indicated that they will continue to dispense mifepristone regardless of the order in Texas unless the FDA tells them they cannot.As requested by plaintiffs in the Washington case, the FDA could also start the process to remove the unnecessary barriers to accessing mifepristone, which every relevant medical organization agrees are not medically necessary. These barriers make abortion less accessible without any benefit for patient safety. Though the FDA has repealed parts of these unduly restrictive rules over the last decade, the FDA should abandon the remaining restrictions, which are also contradicted by the best evidence. These policies do not make the agency seem evenhanded; they make it seem unscientific. The agency should not wait for the Washington court to order this – it should start the process now.In the pre-emption cases, the FDA could help the effort to restore access to early abortion in states with abortion bans by embracing the theory that the federal agency’s regulation of medication abortion trumps state law. The Department of Justice has already signaled its agreement, but the FDA has been silent. The FDA has spent decades assessing the risks and benefits of medication abortion, examining and re-examining the evidence even decades after its approval in 2000. States should not be able to override that authority and create a public health crisis by banning a safe and effective medication.The agency, however, has appeared unwilling to remove the remaining unnecessary barriers to mifepristone or support pre-emption at this juncture. Indeed, it has said nothing about pre-emption and is opposing the attorneys general in the Washington case – a fact that may surprise people who think the Biden administration is doing all it can to support abortion access. Given the current public health crisis, the FDA must be bolder in its support of reproductive healthcare.Try as it might, the FDA cannot escape the abortion debate. Instead of trying to play both sides, the agency must act now by following the science and protecting the public’s health to the best of its ability. Protecting access to safe abortion is the way to do that.
    David S Cohen, a law professor at Drexel University, is a co-author of Obstacle Course: The Everyday Struggle to Get an Abortion in America, a board member of the Abortion Care Network and a consulting attorney with the Women’s Law Project
    Greer Donley is a law professor at the University of Pittsburgh and a board member of the Women’s Law Project
    Rachel Rebouché is the dean of the Temple University Beasley School of Law and a faculty fellow at the Center for Public Health Law Research More

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    Biden team to propose strict vehicle pollution limits to boost EV sales

    The Biden administration will propose strict new automobile pollution limits requiring that all-electric vehicles account for as many as two of every three new vehicles sold in the US by 2032 in a plan that would transform the US auto industry.Under the proposed regulation, expected to be released by the Environmental Protection Agency (EPA) on Wednesday, greenhouse gas emissions for the 2027 through 2032 model years for passenger vehicles would be limited to even stricter levels than the auto industry agreed to in 2021.“This is a massive undertaking,” said John Bozzella, the president of the Alliance for Automotive Innovation, told the New York Times, which first reported on the proposed limits. “It is nothing short of a complete transformation of the automotive industrial base and the automotive market.”The auto industry is expected to push back against the plan, which comes nearly two years after carmakers pledged to make electric vehicles comprise half of US new car sales by 2030 as part of a history-making transition from gasoline-powered engines to battery-powered vehicles. Environmental groups have applauded the ambitious limits proposed by the Biden administration.The proposal would require at least 54% of new vehicles sold in the US to be electric by 2030, four percentage points higher than the 2021 goal that the industry previously agreed to, and up to 67% of new vehicles by 2032. The 2021 agreement came after strong pressure from President Biden, who signed an executive order setting a target for half of all new vehicles sold in 2030 to be zero-emissions vehicles.The president also wants automakers to raise gas mileage and cut tailpipe pollution between now and model year 2026, which would be a significant step toward his pledge to cut US planet-warming greenhouse gas emissions in half by 2030.Electric vehicles accounted for only 7.2% of US vehicle sales in the first quarter of the year, but the share of EV sales is on the rise – last year it was 5.8% of new vehicle sales.The EPA declined to offer details ahead of Wednesday’s announcement, but confirmed in a statement that, as directed by Biden’s order, it is “developing new standards that will … accelerate the transition to a zero-emissions transportation future, protecting people and the planet”.The proposed regulation isn’t expected to become final until next year. More

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    US appeals Texas judge’s ruling to suspend abortion pill approval

    The US government on Monday appealed a Texas judge’s decision to suspend the Food and Drug Administration’s 23-year-old approval of a key abortion drug, saying the ruling endangered women’s health by blocking access to a pill long deemed safe.In a filing with the 5th US circuit court of appeals, the Department of Justice (DoJ) called judge Matthew Kacsmaryk’s decision on the drug mifepristone “especially unwarranted” because it would undermine the FDA’s scientific judgment and harm women for whom the drug is medically necessary.The DoJ also said the anti-abortion groups that sought to overturn the FDA’s approval had no right to sue in the first place, saying they could not show they were harmed and had left the approval unchallenged for years.Kacsmaryk’s decision “upended decades of reliance by blocking FDA’s approval of mifepristone and depriving patients of access to this safe and effective treatment, based on the court’s own misguided assessment of the drug’s safety,” the department said.Lawyers for the anti-abortion groups did not immediately respond to requests for comment.Kacsmaryk, a district judge appointed by former Republican president Donald Trump, had ruled on Friday that the FDA exceeded its authority by ignoring mifepristone’s risks and relying on “plainly unsound reasoning” when approving it.The judge, who works in Amarillo, Texas, stayed his ruling for seven days to allow the Biden administration time to appeal.In Monday’s filing, the justice department asked that Kacsmaryk’s stay remain in place until all appeals, including if necessary to the US supreme court, are resolved.Mifepristone is part of a two-drug regimen, also including misoprostol, for medication abortions in the first 10 weeks of pregnancy. The drugs account for more than half of all US abortions.Kacsmaryk ruled just 18 minutes before a federal judge in Washington state issued a contradictory ruling that directed the FDA to keep the drug available in 17 states.In a Monday filing in that case, the justice department asked the judge there to clarify what should happen if Kacsmaryk’s order took effect.The conflicting rulings could foreshadow a resolution by the supreme court, which last June overturned the 1973 Roe v Wade decision, eliminating a constitutional right to abortion.The supreme court has a 6-3 conservative majority. The New Orleans-based fifth circuit also has a conservative reputation, with three-quarters of its active judges appointed by Republican presidents.“This administration stands by the FDA and is prepared for this legal fight, and we will continue our work to protect reproductive rights,” White House spokesperson Karine Jean-Pierre said.Monday’s appeal came in a case brought by anti-abortion groups led by the Alliance for Hippocratic Medicine, which was formed last August.They accused the FDA of failing to consider during its approval process for mifepristone the drug’s safety when used by girls under age 18.The plaintiffs sought a sympathetic court by suing in Amarillo, where Kacsmaryk is the only federal district judge.Kacsmaryk had written critically about Roe v Wade, and the former Christian legal activist’s courtroom is a popular destination for conservatives challenging Biden policies.Twelve US states ban abortion, while 14 others ban it at some point after six to 22 weeks of pregnancy, according to the nonprofit Guttmacher Institute, which supports abortion rights. More

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    AOC urges Biden to ignore Texas ruling suspending approval of abortion drug

    The New York congresswoman Alexandria Ocasio-Cortez said on Sunday there was “an extraordinary amount of precedent” for the Joe Biden White House to ignore a Friday court ruling suspending federal approval of a drug used in medication abortion.Those remarks from the Democratic US House member quickly prompted a threat by the Texas Republican congressman Tony Gonzales to defund certain programs under the federal agency which oversees medication approvals if Biden’s administration did as Ocasio-Cortez suggested.The Biden administration has already said it plans to appeal a Friday ruling from Texas-based federal judge Matthew Kacsmaryk, a conservative appointed by the Donald Trump White House, that blocked the Food and Drug Administration’s (FDA) approval of the drug mifepristone. The FDA approved the drug in 2000, a move that is now being challenged by the Alliance Defending Freedom, a conservative Christian legal group.In urging the Biden administration to decline to enforce the ruling, Ocasio-Cortez noted that the Trump administration had ignored court rulings on immigration issues. She also pointed out that there was a contradicting ruling from a federal judge in Washington state on Friday which blocked the FDA from taking any action to limit access to the drug, virtually ensuring that the US supreme court would settle the matter at some point.“There is an extraordinary amount of precedent for this … The Trump administration also did this very thing. This has happened before,” she said during an appearance on CNN’s State of the Union.“The courts rely on the legitimacy of their rulings. And when they make a mockery of our system, a mockery of our democracy and a mockery of our law, as what we just saw happen in this mifepristone ruling, then I believe that the executive branch, and we know that the executive branch has enforcement discretion, especially in light of a contradicting ruling coming out of Washington.”CNN host Dana Bash said Ocasio-Cortez was offering a “pretty stunning position” and pressed the congresswoman on whether the Biden administration should ignore the ruling if the US supreme court eventually upheld Kacsmaryk’s decision.“I think one of the things that we need to examine is the grounds of that ruling,” she said. “But I do not believe that the courts have the authority … over the FDA that [Kacsmaryk] just asserted. And I do believe that it creates a crisis. Should the supreme court do that, it would essentially institute a national abortion ban.”During a later appearance on State of the Union, Gonzales told Bash that there would be consequences if the Biden administration ignored the ruling.“The House Republicans have the power of the purse,” Gonzales said. “And if the administration wants to not live up to this ruling, then we’re gonna have a problem. And it may become a point where House Republicans on the appropriations side have to defund FDA programs that don’t make sense.”Bash also asked the secretary of the US Department of Health and Human Services, Xavier Becerra, whether ignoring the ruling was “off the table”. Becerra declined to say specifically what the administration would do if appellate courts, including the supreme court, upheld the decision.“Everything is on the table,” he said on CNN. “We want the courts to overturn this reckless decision.” More

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    China sends dozens of warplanes towards Taiwan as US urges restraint amid military drills

    China sent dozens of warplanes towards Taiwan for a second day of military drills on Sunday, launching simulated attacks in retaliation to the island’s president, Tsai Ing-wen, meeting the US House speaker during a brief visit to the US.Taiwan’s defence ministry said it was monitoring the movements of China’s missile forces, as the US said it too was on alert.China’s People’s Liberation Army (PLA) sent 70 warplanes, including fighter jets, reconnaissance craft and refuellers, into Taiwan’s air defence identification zone (ADIZ) on Sunday morning, according to Taiwan’s defence ministry. It did not provide a map or locations, but said 31 planes had crossed the median line – the de facto border in the Taiwan strait between Taiwan and China.The PLA had announced the immediate start to three days of drills on Saturday morning. By 7pm that evening it had sent 71 warplanes and eight ships into Taiwan’s ADIZ with almost 60 crossing the median line.Taiwan’s ministry said the activity had severely violated Indo-Pacific peace and stability, and had a negative effect on international security and economies. It urged other countries to speak out against China’s actions.Chinese state television reported that multiple units carried out simulated strikes on key targets in Taiwan and the surrounding sea. The Chinese military’s eastern theatre command put out a short animation of the simulated attacks on its WeChat account, showing missiles fired from land, sea and air into Taiwan with two of them exploding in flames as they hit their targets.A Taiwan security source told Reuters that on Saturday the Chinese drills around the Bashi channel, which separates Taiwan from the Philippines, included simulated attacks on aircraft carrier groups as well as anti-submarine drills.Last August, after a visit to Taipei by then US House speaker Nancy Pelosi, China staged war games around Taiwan including firing missiles into waters close to the island, though it has yet to announce similar drills this time.Chinese maritime authorities have issued just one notice of a live fire zone, in a small area of water near Pingtan, in the Taiwan strait. The mandatory notice warns air and seacraft to keep clear of the area, which is just a fraction of the areas designated for live fire during last year’s drills.While in Los Angeles last week, on what was officially billed a transit on her way back from Central America, Tsai met the speaker of the US House of Representatives, Kevin McCarthy, despite Beijing’s warnings against the meeting.The de facto US embassy in Taiwan said on Sunday that the US was monitoring China’s drills around Taiwan closely and is “comfortable and confident” it has sufficient resources and capabilities regionally to ensure peace and stability.US channels of communication with China remain open and the US had consistently urged restraint and no change to the status quo, said a spokesperson for the American Institute in Taiwan, which serves as an embassy in the absence of formal diplomatic ties.Washington severed diplomatic relations with Taipei in favour of Beijing in 1979 but is bound by law to provide the island with the means to defend itself.China, which has never renounced the use of force to bring the island under its control, says Taiwan is the most important and sensitive issue in its relations with the US, and the topic is a frequent source of tensions.Beijing considers Tsai a separatist and has rebuffed her repeated calls for talks. Tsai says only Taiwan’s people can decide their future.China has over the past three years or so stepped up its military pressure against Taiwan, flying regular missions around Taiwan, though not in its territorial airspace or over the island itself.Chinese state media said the aircraft flown into the ADIZ this weekend were armed with live weapons.Taiwanese air force jets also typically carry live weapons when they scramble to see off Chinese incursions.Late on Saturday, Taiwan’s Ocean Affairs Council, which runs the coast guard, put out footage on its YouTube channel showing one of its ships shadowing a Chinese warship, though it did not give an exact location.“You are seriously harming regional peace, stability and security. Please immediately turn around and leave. If you continue to proceed we will take expulsion measures,” a coast guard officer says by radio to the Chinese ship.Other footage showed a Taiwanese warship, the Di Hua, accompanying the coast guard ship in what the coast guard officer calls a “standoff” with the Chinese warship.Still, civilian flights around Taiwan, including to Kinmen and Matsu, two groups of Taiwan-controlled islands right next to the Chinese coast, have continued as normal.In August, civilian air traffic was disrupted after China announced effective no-fly zones in several areas close to Taiwan where it was firing missiles.Meanwhile the French president, Emmanuel Macron, said in an interview published on Sunday that Europe must not be a “follower” of either the US or China on Taiwan, saying that the bloc risks entanglement in “crises that aren’t ours”.His comments risk riling Washington and highlight divisions in the European Union over how to approach China, as the US steps up confrontation with its closest rival and Beijing draws closer to Russia in the wake of its invasion of Ukraine.“The worst thing would be to think that we Europeans must be followers and adapt ourselves to the American rhythm and a Chinese overreaction,” Macron told media as he returned on Friday from a three-day state visit to Beijing.Reuters contributed reporting More