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    Axis Dance Explores New Frontiers With Mobility Technology

    What are crutches for? To help an injured or disabled person get from Point A to Point B?Like most mobility devices, crutches are often designed and viewed in a matter-of-fact medical framework. There is a problem to be fixed; the device is the solution.Performances by Axis Dance Company routinely explode that idea. For Axis — an Oakland, Calif., ensemble of both disabled and non-disabled dancers — a crutch brims with creative possibilities: It might be a partnering support, a third leg, an elongated arm.But what happens when that expansive way of thinking is applied to the design of the device itself? What kinds of movement might be possible if, for example, a crutch could extend and retract?Joseph Tebandeke (aloft) and Anna Gichan of Axis rehearsing. That’s not a hypothetical. Telescoping crutches play a central role in Axis’ “Kinematic/Kinesthetic,” premiering Thursday at the Exploratorium museum in San Francisco. The work is a collaboration between the interdisciplinary artist Ben Levine; the choreographer and Axis artistic director Nadia Adame; and engineering students from Carnegie Mellon University and the University of Maryland. It features two imaginative mobility technologies developed for the project — the telescoping crutches, and a hexapod robot that gives its user six legs rather than two — as well as a hands-free Omeo wheelchair.Levine, who is disabled, hopes “Kinematic/Kinesthetic” will enlarge our understanding of the relationship between bodies and machines. Dancers are deeply attuned to their physical selves; people with disabilities often interact extensively with technology. Involving these knowledgeable bodies in the development of assistive devices can reshape ideas about the devices — and potentially generate new ways of moving.We are having trouble retrieving the article content.Please enable JavaScript in your browser settings.Thank you for your patience while we verify access. If you are in Reader mode please exit and log into your Times account, or subscribe for all of The Times.Thank you for your patience while we verify access.Already a subscriber? Log in.Want all of The Times? Subscribe. More

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    Trump Cuts Threaten Meals and Services for People With Disabilities and the Aging

    Every Monday, Maurine Gentis, a retired teacher, waits for a delivery from Meals on Wheels South Texas.“The meals help stretch my budget,” Ms. Gentis, 77, said. Living alone and in a wheelchair, she appreciates having someone look in on her regularly. The same group, a nonprofit, delivers books from the library and dry food for her cat.But Ms. Gentis is anxious about what lies ahead. The small government agency responsible for overseeing programs like Meals on Wheels is being dismantled as part of the Trump administration’s overhaul of the U.S. Department of Health and Human Services. Roughly half its staff has been let go in recent layoffs and all of its 10 regional offices are closed, according to several employees who lost their jobs.“I’m just kind of worried that the whole thing might go down the drain, too,” Ms. Gentis said.In President Trump ’s quest to end what he termed “illegal and immoral discrimination programs,” one of his executive orders promoted cracking down on federal efforts to improve accessibility and representation for those with disabilities, with agencies flagging words like “accessible” and “disability” as potentially problematic. Certain research studies are no longer being funded, and many government health employees specializing in disability issues have been fired.The downsizing of the agency, the Administration for Community Living, is part of far-reaching cuts planned at the H.H.S. under the Trump administration’s proposed budget.While some federal funding may continue through September, the end of the government’s fiscal year, and some workers have been called back temporarily, there is significant uncertainty about the future. And some groups are reporting delays in receiving expected federal funds.We are having trouble retrieving the article content.Please enable JavaScript in your browser settings.Thank you for your patience while we verify access. If you are in Reader mode please exit and log into your Times account, or subscribe for all of The Times.Thank you for your patience while we verify access.Already a subscriber? Log in.Want all of The Times? Subscribe. More

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    Amadou Bagayoko, Half of Malian Duo Who Went Global, Dies at 70

    As Amadou & Mariam, he and his wife were improbable pop stars on two counts. Their style was venturesome and eclectic, and they were blind virtuosos.Amadou Bagayoko, a Malian guitarist and composer who with his wife, the singer Mariam Doumbia, formed Amadou & Mariam, inventing a broadly accessible sound that made fans of people worldwide who otherwise knew little about music from Africa, died on Friday in Bamako, Mali’s capital. He was 70.His death was announced by the Malian government, which did not provide a cause. He and Ms. Doumbia lived in Bamako.In the late 2000s and early 2010s, Amadou & Mariam was regularly described as the new century’s most successful African musical act.Mr. Bagayoko, who grew up listening to Led Zeppelin and Pink Floyd, called their sound “Afro-rock,” and the group regularly combined his winding guitar solos with, for example, the pounding of a West African djembe drum.Yet the group’s music also consistently evolved. Their breakout hit, the 2005 album “Dimanche à Bamako,” had chatty spoken asides, sirens, the hubbub of crowds — city sounds turned into melodies. Their 2008 album “Welcome to Mali,” conversely, embraced an electronic style of funk, opening with a song, “Sabali,” featuring Damon Albarn of the arty hip-hop group Gorillaz.What was consistent was a sweet, graceful sound that still had the power to build to crescendos, with Ms. Doumbia’s alto achieving clear, pleasant resonance over a rich orchestration.We are having trouble retrieving the article content.Please enable JavaScript in your browser settings.Thank you for your patience while we verify access. If you are in Reader mode please exit and log into your Times account, or subscribe for all of The Times.Thank you for your patience while we verify access.Already a subscriber? Log in.Want all of The Times? Subscribe. More

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    UK Aims to Cut Billions in Welfare Amid Budget Crunch

    Changing disability allowances is a particularly contentious move within Prime Minister Keir Starmer’s center-left Labour Party.Britain’s center-left government outlined plans on Tuesday to curb spiraling welfare costs as it attempts to juggle a difficult set of competing objectives: saving public money, incentivizing work and protecting the most vulnerable.The announcement follows weeks of tense internal debate within the governing Labour Party, led by Prime Minister Keir Starmer, about how to cut Britain’s spending on welfare, which has risen sharply since the Covid-19 pandemic.“The status quo is unacceptable but it is not inevitable,” Liz Kendall, the work and pensions secretary, said in Parliament, promising “decisive action” to get those who can work into employment, protect those who cannot, and save five billion pounds (about $6.5 billion) by 2030.For Labour, a party that sees itself as the creator and guardian of Britain’s post-World War II welfare state, cutting support for some of the most vulnerable in society is especially contentious.But Britain, with a total population of about 68 million, now has more than 9.3 million people of working age across England, Scotland and Wales who are not employed, a rise of 713,000 since 2020. Of those, 2.8 million receive long-term sickness payments or related welfare, according to the government, which expects the number to grow to more than four million if nothing is done. The government spent £65 billion on sickness payments last year.Facing mounting pressure to increase military spending, at a time when public services including the health system are badly underfunded, and economic growth is sluggish, Britain’s Treasury is searching for cuts to public programs.We are having trouble retrieving the article content.Please enable JavaScript in your browser settings.Thank you for your patience while we verify access. If you are in Reader mode please exit and log into your Times account, or subscribe for all of The Times.Thank you for your patience while we verify access.Already a subscriber? Log in.Want all of The Times? Subscribe. More

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    Trump’s USAID Cuts Halt Agent Orange Victims Program in Vietnam

    Nearly 40 years after she was born with a malformed spine and misshapen limbs — most likely because her father was exposed to Agent Orange, the toxic chemical that the American military used during the Vietnam War — Nguyen Thi Ngoc Diem finally got some help from the United States.A project funded by U.S.A.I.D. gave her graphic design training in 2022 and helped her land a job. Even when the company closed a few months ago, she stayed hopeful: The same program for Agent Orange victims was due to deliver a new computer, or a small loan.I was the first to tell her that the support may never come; that President Trump had frozen U.S.A.I.D. funding and planned to fire nearly everyone associated with the humanitarian agency.“It makes no sense,” Ms. Diem told me, her tiny body curled into a wheelchair, below a crucifix on the wall. “Agent Orange came from the U.S. — it was used here, and that makes us victims,” she said. “A little support for people like us means a lot, but at the same time, it’s the U.S.’s responsibility.”Ms. Diem had been expecting a small U.S. loan to help her buy a more modern computer for her graphic design work.Linh Pham for The New York TimesMs. Diem uses a computer from 2011. It often freezes and shuts down unexpectedly.Linh Pham for The New York TimesWe are having trouble retrieving the article content.Please enable JavaScript in your browser settings.Thank you for your patience while we verify access. If you are in Reader mode please exit and log into your Times account, or subscribe for all of The Times.Thank you for your patience while we verify access.Already a subscriber? Log in.Want all of The Times? Subscribe. More

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    Special Education Services With a Catch: Parents Are Asked Not to Sue

    New York City school officials want families seeking such services to waive their right to sue the Education Department in exchange for receiving them. New York City parents who missed a rarely enforced deadline to apply for their children’s special education services can now receive those services, but only if they agree not to sue the Education Department.The requirement affects about 3,500 families whose children attend private or religious schools or are home-schooled and receive resources such as teacher aides who attend class with them, speech therapy and occupational therapy.About 17,000 families successfully filed to participate in the system this year by the June 1 deadline, which had not been enforced in previous years. The families who missed the cutoff were left in limbo.Because they missed the deadline, their children have not gotten the services so far this school year. The waiver, which the Education Department sent to affected parents on Thursday, would provide the families expedited services in about three days, said Nicole Brownstein, a spokeswoman for the city Education Department.But one lawyer who specializes in education issues described the waiver as “highly problematic” because of its vague wording, and another said such a pre-emptive move was extremely unusual. City Council members learned about the new waiver program during a briefing on Thursday.“I think it’s outrageous,” said Councilman Keith Powers, who attended the meeting with the Education Department. He added, “It feels wrong, and the whole process has been a mess from the very beginning.”We are having trouble retrieving the article content.Please enable JavaScript in your browser settings.Thank you for your patience while we verify access. If you are in Reader mode please exit and log into your Times account, or subscribe for all of The Times.Thank you for your patience while we verify access.Already a subscriber? Log in.Want all of The Times? Subscribe. More

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    Daniel Romanchuk’s Pre-Marathon Routine Includes Sandpaper

    Many of the 50,000 entrants in the New York City Marathon have pre-race routines — carbo-loading, plenty of liquids and so on — but only a few of these routines include wrenches, Allen keys and sandpaper.Daniel Romanchuk checks the contents of his utility pouch in Central Park ahead of the NYC Marathon, Manhattan, 2024.Clark Hodgin for The New York TimesThose are just a few of the tools that the 40 or so professional wheelchair racers rely on to prepare for New York’s hilly and rough roads.Before every race, they tighten the various nuts and bolts on their chairs to make sure nothing rattles lose on the city’s streets and bridges. Tires are doubled checked to ensure they are properly inflated. Adhesives are applied to customized racing gloves.Clark Hodgin for The New York Times“I have a nice long list of everything I need,” said Daniel Romanchuk, who became in 2018 the first American and youngest athlete ever to win the men’s wheelchair division in New York. “I travel with every tool that I could possibly need.”Clark Hodgin for The New York TimesClark Hodgin for The New York TimesUnlike at the Olympics, where there are fix-it shops to help Paralympians in a pinch, there is no dedicated wheelchair repair shop at the New York City Marathon. But by necessity, the racers and their coaches have an intimate knowledge of their wheelchairs and come prepared with an array of tools to allow them to make fixes on the fly.Clark Hodgin for The New York TimesIn addition to wrenches and screwdrivers, racers pay close attention to their tires, making sure they are ready for New York’s potholes and bridges. The organizers provide cans of pressurized CO2 because racers cannot bring them on planes when they travel to New York. Mr. Romanchuk recently switched to tubeless tires, but other racers carry sealant to repair any punctures.Clark Hodgin for The New York TimesRacers also apply adhesive to their gloves, but there is a balance between adding too much and too little, especially if it rains and grips become slippery.Clark Hodgin for The New York Times“I did that in one race when I was expecting it to rain a lot and it barely did, and my glove would stick to the wheel,” Mr. Romanchuk said.The night before the race, officials meet in the athletes’ hotel to inspect every chair to ensure it meets race standards for things like wheel size.Clark Hodgin for The New York TimesRomanchuk inspects the bottom of his racing bikeClark Hodgin for The New York TimesClark Hodgin for The New York TimesThe next morning, the chairs are brought to the hotel lobby and loaded onto trucks and taken to start line. The racers then travel by bus to Staten Island, where they do their final preparations, including packing a few essential tools like an Allen key and small CO2 can to carry during the race.Daniel Romanchuk poses for a photo for his mother at the finish line on Friday before the race.Clark Hodgin for The New York Times More

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    Doctors, A.I. and Empathy for Patients

    More from our inbox:Breast Cancer ScreeningWalz’s MisstepsMental Health Support for SchoolchildrenTo the Editor:Re “ChatGPT’s Bedside Manner Is Better Than Mine,” by Jonathan Reisman (Opinion guest essay, Oct. 9):Dr. Reisman notes that ChatGPT’s answers to patient questions have been rated as more empathetic than those written by actual doctors. This should not be a call for doctors to surrender our human role to A.I. To the contrary, we need to continue to improve our communication skills.For the past 25 years, I have been facilitating seminars in doctor-patient communication. The skills to communicate bad news listed by Dr. Reisman are exactly the techniques that we suggest to our medical students. However, doctors can avoid the temptation to surrender their “humanity to a script” as if it were “just another day at work.”Techniques are a valuable guide, but the real work consists of carefully listening to the responses and their emotional content, and crafting new words and phrases that speak to the unique patient’s confusion, fear and distress.In my experience, patients know when we are reciting a script, and when we are paying attention to their thoughts and feelings. Unlike A.I., and especially when conversations are matters of life and death, we can reach into the depths of our humanity to feel and communicate empathy and compassion toward our patients.Neil S. ProseDurham, N.C.To the Editor:Mention the words “A.I.” and “doctoring” to most physicians in the same sentence, and the immediate reaction is often skepticism or fear.As Dr. Jonathan Reisman noted in his essay, A.I. has shown a remarkable ability to mimic human empathy in encounters with patients. This is one reason many practicing physicians worry that A.I. may replace doctors eventually.We are having trouble retrieving the article content.Please enable JavaScript in your browser settings.Thank you for your patience while we verify access. If you are in Reader mode please exit and log into your Times account, or subscribe for all of The Times.Thank you for your patience while we verify access.Already a subscriber? Log in.Want all of The Times? Subscribe. More