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      John Korty, Director of ‘Miss Jane Pittman,’ Is Dead at 85

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      He was best known for a series of ambitious television movies that examined racism, disability and other social issues.John Korty, a director best known for ambitious made-for-television projects, including the 1974 film “The Autobiography of Miss Jane Pittman,” which won nine Emmy Awards, died on March 9 at his home in Port Reyes Station, Calif. He was 85.His brother, Doug Korty, said the cause was vascular dementia.“Miss Jane Pittman,” a CBS presentation based on the Ernest J. Gaines novel in which a Black woman recounts more than a century’s worth of memories, featured an acclaimed performance by Cicely Tyson as the title character. John J. O’Connor, reviewing the film in The New York Times, called it “a splendid night for television.”“John Korty’s direction is cool and restrained,” he added, “never underlining and always avoiding what could easily be mawkish.”The Emmys the film won included one for Mr. Korty for best directing of a single program, comedy or drama.Mr. Korty on the set of the 1974 television movie  “The Autobiography of Miss Jane Pittman,” which went on to win nine Emmy Awards, including one for Mr. Korty.via Korty Family Cicely Tyson as the title character, a woman who recounts more than a century’s worth of memories, in “The Autobiography of Miss Jane Pittman.”Bettmann via GettyMr. Korty also won both an Oscar and an Emmy for “Who Are the Debolts? And Where Did They Get 19 Kids?,” a documentary about a couple whose many children included hard-to-place adopted ones with disabilities or other challenges. American television networks weren’t interested in the documentary when Mr. Korty first offered it; it was initially released as a film in Japan, then shown at the San Francisco Film Festival in 1977, where it received a standing ovation.That brought it an Oscar for best documentary feature, but Mr. Korty still wanted to get it in front of TV audiences. With some persuasion from Henry Winkler, whose role as Fonzie on “Happy Days” had made him one of the network’s biggest stars, ABC finally broadcast a cut-down version in late 1978; that version won the Emmy for outstanding individual achievement for an informational program.Although Mr. Korty also directed lighter fare and the occasional Hollywood feature, including “Oliver’s Story,” the 1978 follow-up to the hit 1970 movie “Love Story,” he gravitated toward television movies that touched on social issues.In addition to “Miss Jane Pittman,” which covered a century’s worth of the Black experience, he directed “Go Ask Alice” (1973), about teenage drug addiction; “Farewell to Manzanar” (1976), about the internment of Japanese Americans during World War II; “Second Sight: A Love Story” (1984), about a blind woman; “Resting Place” (1986), about a family’s attempt to have a Black officer who was killed in Vietnam buried in his hometown’s all-white cemetery; and “Eye on the Sparrow” (1987), about a blind couple trying to adopt.“I wouldn’t give up television movies,” Mr. Korty told The Times in 1986. “There is nothing like the response you get. Fifty million people saw ‘Jane Pittman’ in one night. That’s very different from even the biggest hit movie.”Mr. Korty on the set of “Farewell to Manzanar,” his 1976 TV movie about the internment of Japanese Americans during World War II.via Korty FamilyIn the best of his television work, Mr. Korty sought to illuminate subjects and perspectives not often addressed in the mainstream. In an essay he wrote for The San Francisco Examiner in 1978, he said that was his hope for the “Debolts” film, in which he showed the children’s disabilities in unflinching detail, rare for TV at the time.“It seems that most physically handicapped people have their greatest struggles not with their crutches, but with their identities — being accepted as individuals rather than as a distasteful class of outcasts,” he wrote. “We hope that by the end of our film the audience will forget who is on crutches and who isn’t.”John Van Cleave Korty was born on June 22, 1936, in Lafayette, Ind. His father, Richard, was an engineer, and his mother, Mary (Van Cleave) Korty, was a nurse.“I started drawing when I was 5 years old,” Mr. Korty said at a 2013 panel discussion of his work, “and for many, many years I thought I was going to be what you’d call a commercial artist.”But in 11th grade a teacher showed the class some of the innovative animated films of Norman McLaren, and Mr. Korty found a new interest. He soon made his first animated film, but, as he told The Abilene Reporter-News of Texas in 1986, he couldn’t afford new film stock. Instead he somehow obtained a reel of a Mickey Mouse cartoon and dumped bleach on it in his parents’ bathtub to erase the images, then hand-painted images on its 2,600 frames. The trick worked, he said, but it took him a week to scrub the bathtub clean.He earned a bachelor’s degree at Antioch College, where he continued to experiment with animation. In about 1963 he settled in the Bay Area, where he set up his own studio. One of his earliest professional efforts, “Breaking the Habit,” a documentary about smoking produced in cooperation with the American Cancer Society, was nominated for the short-subject documentary Oscar in 1965.Mr. Korty directed the independent features “The Crazy-Quilt” (1966), “Funnyman” (1967) and “riverrun” (1968) before he made his first television movies, drawing some critical acclaim and the attention of other young filmmakers who were interested in working outside the Hollywood system. Among them were Francis Ford Coppola and George Lucas, who came to visit his setup in 1968.“They showed up in two station wagons, and when Francis walked in, his mouth dropped open,” Mr. Korty told The Marin Independent Journal in 2011. “He said, ‘My God, you’ve done exactly what we want to do: get out of Hollywood and set up a studio. If you can do it, we can do it.’”A year later Mr. Coppola and Mr. Lucas would found their American Zoetrope studio in San Francisco. Mr. Korty had an office there for several years and went on to work with Mr. Lucas. He and Charles Swenson directed “Twice Upon a Time,” an animated feature made with Mr. Lucas’s Lucasfilm company in 1983, and the next year Mr. Korty directed “Caravan of Courage,” a Lucasfilm TV movie based on the Ewok creatures from the “Star Wars” movie “Return of the Jedi.”“I wouldn’t give up television movies,” Mr. Korty said in 1986. “There is nothing like the response you get. Fifty million people saw ‘Jane Pittman’ in one night. That’s very different from even the biggest hit movie.”via Korty FamilyThough the success of “Miss Jane Pittman” brought Mr. Korty offers to direct Hollywood films, he rarely accepted. “Oliver’s Story,” which he directed in 1978, was an exception. It was a bigger-budget movie than he normally attempted, with big stars — Ryan O’Neal, Candice Bergen — and Mr. Korty wasn’t entirely comfortable.“It’s the first movie I’ve ever made that I’ve felt not a part of,” he told The Sacramento Bee in December 1978 as the early reviews, many of them unflattering, were coming in. “I know I put things in this movie that I liked and the audience wouldn’t — and vice versa.”Mr. Korty’s marriages to Carol Tweedie in 1959 and Beulah Chang in 1965 ended in divorce. In 1989 he married Jane Silvia, who survives him, along with his brother; a sister, Nancy Korty; two sons from his second marriage, Jonathan and David; a son from his third marriage, Gabriel; and three grandchildren. More

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      Jack Willis, TV Producer and Empathetic Filmmaker, Dies at 87

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      A survivor of a crippling accident, his documentaries and news coverage for public television focused on poverty, race and other social issues.Jack Willis, a journalist and television executive who won several Emmys and a Polk Award for his innovative films and news and documentary programming during the embryonic years of cable and public broadcasting, died on Feb. 9 in Zurich. He was 87.He underwent assisted suicide at a clinic there, his wife, Mary Pleshette Willis, said. He lived in Manhattan.When he was in his late 30s, Mr. Willis broke his neck in a body surfing accident that temporarily left him a quadriplegic before he miraculously recovered, his wife said, inspiring a television movie. But after a half century, the injuries were taking their toll. Six years ago, he broke his hip and began using a wheelchair, she said.From 1971 to 1973, Mr. Willis was director of programming and production for WNET, the public television station in New York, where he introduced innovative local news coverage as executive producer of “The 51st State,” a program that took its name from the zany 1969 mayoral campaign of the author Norman Mailer, who proposed that New York City secede from New York State.The program, which won an Emmy Award, focused on communities rather than the more traditional fare of the nightly local news.Patrick Watson, center, the anchor of the WNET program “The 51st State,” moderated a discussion of racial tensions in New York City in 1971. Mr. Willis was the program’s executive producer. WNET records, Special Collections, University of Maryland Libraries“He pioneered in-depth local coverage of New York’s outer boroughs on WNET, focusing on long-ignored and disenfranchised minorities and immigrants, often letting them speak for themselves,” said Stephen B. Shepard, former editor in chief of Business Week and founding dean of the City University of New York Graduate School of Journalism. “For Jack, it was always about the people affected by government decisions.”Mr. Willis was an executive producer of another Emmy-winning series, “The Great American Dream Machine,” a weekly 90-minute program on PBS. The television critic John J. O’Connor of The New York Times, writing in 1971, said the program had been conceived as “a free‐form program that could offer the viewer worthwhile bits and pieces of humor, controversy, entertainment, investigative reporting, opinion, documentary and theatrical sketches.”“It has been called a hodgepodge of the brilliant and the trite,” he added, but concluded that it was “one of the most exciting and imaginative segments of television to come along this season.”Looking back, Mr. Willis himself told The Times in 2020: “It was a great time in public television. If you thought it, you could do it.”Marshall Efron, left, and Andy Rooney, two of the stars of the PBS program “The Great American Dream Machine,” in 1972. Mr. Willis was its executive producer. WNETIn 1963, he directed his first documentary, “The Streets of Greenwood,” a 20-minute film about a voter-registration drive in the Mississippi Delta. Collaborating with two friends, Phil Wardenburg and John Reavis, Mr. Willis shot it with a camera he had borrowed from the folk singer Pete Seeger, whose concert in a cotton field was featured in the film.In 1979, Mr. Willis shared the George Polk Award for best documentary with Saul Landau for “Paul Jacobs and the Nuclear Gang.” The film focused on the journalist Paul Jacobs’s investigation of radiation hazards from atomic testing in Nevada in the 1950s and ’60s and the federal government’s efforts to suppress information on its threat to public health.Two other films he produced — “Lay My Burden Down” (1966), about the plight of tenant farmers in rural Alabama, and “Every Seventh Child” (1967), questioning tax subsidies and other government benefits for Catholic education — were shown at the New York Film Festival.Mr. Willis wrote, directed and produced “Appalachia: Rich Land Poor People” (1968), which exposed grinding poverty largely caused, the film argued, by corporate greed, racism and ineffective local government.Mr. Willis’s commitment to civil rights was reflected in his enduring friendship with the singer Harry Belafonte, an activist in the movement, who described Mr. Willis in an email as “a soul brother” whose “intellect and humor, combined with his courageousness, make him one of the most precious people I have ever known.”“For those on the political left,” Mr. Belafonte added, “he was living proof of the proverb, ‘You can cage the singer but not the song.’”Jack Lawrence Willis was born on June 20, 1934, in Milwaukee to Louis Willis, a manufacturer of women’s shoes, and Libbie (Feingold) Willis, a homemaker. The family moved to California when he was 9.He earned a bachelor’s degree in political science in 1956 from the University of California, Los Angeles, where he also played shortstop on the varsity baseball team. He liked to recall that he was recruited by a Boston Red Sox minor-league team.Mr. Willis dropped out of U.C.L.A. School of Law to serve in the Army for two years, then graduated in 1962 and moved to New York, where he hoped to connect with a job teaching in Africa or the Middle East.While waiting for a job abroad that never materialized, he worked briefly in television for Allen Funt’s “Candid Camera” and David Susskind’s “Open End.”He ran a movie production company in California, then was hired as vice president for programming and production at CBS Cable, a short-lived but well-received performing arts channel.From 1990 to 1997, Mr. Willis was president of KTCA, the public television station in Minneapolis-St. Paul, then returned to New York, where, working for George Soros’s Open Society Institute, he developed a media program. In 1999, he was a founder of Link TV, a nonprofit satellite TV network. He retired in 2011.Jack Willis in an undated photo. via Mary WillisIn addition to his wife, he is survived by their two daughters, Sarah Willis and Kate Willis Ladell; three grandchildren; and his brother, Richard.Mr. Willis and his wife wrote a book, “… But There Are Always Miracles” (1974), about his body-surfing accident in 1969 off Southampton, N.Y. They had been planning to marry when a crashing wave broke his neck and left him paralyzed from the chest down. He was told he would never walk again.After two operations and six months of inpatient rehabilitation, he walked out of Rusk Institute of Rehabilitation Medicine in Manhattan. The couple married a year later.His story was adapted into a TV film, “Some Kind of Miracle” (1979), with a screenplay by the couple. They wrote and produced other films together.Shortly before he died, Ms. Willis said, her husband told her that the accident had “taught me to put everything in perspective — including the fear of failure.” He admitted to no regrets, she said, “except,” she quoted him as saying, “for taking that wave and turning down the Boston Red Sox.” More

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      in Movies

      Troy Kotsur Makes History as the First Deaf Actor to Get a Nomination

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      A couple of weeks ago in The Hollywood Reporter, Troy Kotsur compared the opportunities for deaf actors like himself to one small hair in a beard’s worth of roles for those who can hear.With Sian Heder’s “CODA,” which stands for Child of Deaf Adults, he plucked it and made history. He’s the first deaf actor to be nominated for an Oscar. In 1987, Marlee Matlin became the first deaf performer to be nominated; she went on to win the Oscar, for “Children of a Lesser God.” Matlin happens to be Kotsur’s co-star in “CODA.”Kotsur plays Frank Rossi, a deaf fisherman, gruff yet surprisingly tender, trying to keep his business in Gloucester, Mass., afloat with the help of his teenage daughter, Ruby (Emilia Jones), the only hearing member of their family. Ruby has served as the interpreter for Frank, her mother, Jackie (Matlin), and her brother, Leo (Daniel Durant) for most of her life. But she longs to go to music school and become a singer, a dream her parents can’t understand. (“If I were blind, would you paint?” Jackie asks.) And the thought of having to navigate life on their own is terrifying.The critical response to Kotsur’s portrayal has been overwhelmingly warm. Owen Gleiberman of Variety called him “an extraordinary actor”; Steve Pond of The Wrap declared him “a treasure as Matlin’s gloriously profane husband”; and Peter Travers of “Good Morning America” said he was “hilarious and heartbreaking.”The role has also earned Kotsur 31 nominations, including a BAFTA, a Golden Globe, the first Screen Actors Guild nod for an individual deaf male actor and now an Oscar for best supporting actor. So far he has tallied nine wins, including a Gotham Award and a Spotlight Award from the Hollywood Critics Association.In a statement on Tuesday after the Oscar nominations were announced, Kotsur said he was stunned, explaining, “I can still remember watching Marlee win her Oscar on television and telling friends I was going to get nominated one day and them being skeptical. I would like to thank everyone for this huge honor.”Despite the scarcity of jobs for deaf actors, Kotsur is not exactly a stranger to the limelight. In 2003, he shared the role of Pap with a hearing actor in the Tony-nominated 2003 American Sign Language adaptation of “Big River” on Broadway. More recently he helped to develop a sign language for the Tusken Raiders in “The Mandalorian.”Still, “I’m so glad that they recognized me,” Kotsur told The Hollywood Reporter of the accolades that have come his way, “not because I’m deaf but because I’m a talented actor.” More

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      in Television

      A New Coalition Amplifies Disability Culture in the Music Industry

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      RAMPD, an organization of professional disabled musicians, will push for accessibility in the music industry, including adding visible ramps to awards show stages.For the singer, songwriter and producer Lachi, the acronym was everything.She helped start the organization that would become RAMPD — Recording Artists and Music Professionals with Disabilities — in July 2021, but it was a few months earlier, after moderating a panel for the Recording Academy about disability inclusion, that she came up with the name.“After that aired, musicians with disabilities were coming out of the woodwork and following me on Instagram, DMing me going, ‘What are we going to do? Are you going to lead this charge? What’s next?’” Lachi said in an interview. “Everyone was energized. And that’s when the spark came, of the acronym.”RAMPD, which Lachi co-founded with the singer-songwriter and violinist Gaelynn Lea, alongside a dozen or so founding members, works to amplify disability culture and advocate for accessibility in the music business. One of its main goals, fittingly, is to make accessibility ramps visible on TV during awards shows to help normalize disability in the entertainment industry.The coalition’s kickoff will be a virtual event at 5 p.m. on Friday, with opening and closing remarks live from the Grammy Museum Experience at the Prudential Center in Newark, N.J. (The Grammy Awards, originally scheduled for Jan. 31, have been pushed back to April 3.) Adrian Anantawan, a classical violinist; Eliza Hull, an indie rock singer-songwriter; and Molly Joyce, an organist and songwriter, will perform, alongside other disabled musicians, and professional membership applications for the group will open.“Our professional membership have awards, have toured, have worked with big names, are big names themselves,” said Lachi, who is based in New York. “And we’re not here to make folks feel warm and gushy. We’re not here to get handouts. We’re here to get gigs. We’re here to get on stages, we’re here to get paid.”“Disability isn’t ‘despite this, they did this,’” said the singer-songwriter and violinist Gaelynn Lea, a RAMPD co-founder. “It’s more like, ‘because of their identity as a disabled artist, you are enjoying this art in this form.’” Paul VienneauIn October, RAMPD partnered with the inaugural Wavy Awards for an event celebrating women, L.G.B.T.Q. artists, nonbinary musicians, artists of color, performers who identify as having a disability and allies. The organization advised the show on American Sign Language interpretation, captioning, audio description and ensuring the inclusion of people with disabilities on-camera and behind the scenes.Perhaps Lachi’s favorite part, though, was promoting the use of what she calls “self description,” known widely as visual description, which is added as audio to television programs and movies to help people with low vision and people who are blind, like herself.“My name is Lachi, she/her, Black girl, cornrows,” she said as an example. “So that’s what I go by. And that’s all it is.”She underscored how racism, sexism and homophobia compound the discrimination disabled people face. “It’s paramount for folks to recognize that disability has color, that disability has gender, that disability has sexual preference and that disability is not straight, white, middle-America male,” she said.Lea, who was born with osteogenesis imperfecta and is based in Minnesota, pointed out that she wouldn’t make the same music — which won NPR Music’s Tiny Desk Contest in 2016 — if not for her life experience.“Disability isn’t ‘despite this, they did this,’” she said in an interview. “It’s more like, ‘because of their identity as a disabled artist, you are enjoying this art in this form.’”She added, “Disability culture and the movement that we’re starting I think really is actually up there in terms of cultural shifts with all the other diversity movements we’re talking about.”Through the Arrowhead Regional Arts Council in Duluth, Minn., Lea received the Arts Ecosystem Grant, which will allow RAMPD to build a membership database of professional disabled artists — something that never existed until now. RAMPD also recently secured a fiscal sponsor, Accessible Festivals, a nonprofit organization that will help manage RAMPD’s grants and donations, and allow for the group to grow beyond Lachi and Lea.“We want to see more leaders emerge out of this and people recognize them in the community, because sometimes it feels like I get asked to do so many events, and it’s partly because I feel like people don’t know anyone else to ask,” Lea said. “That’s something that we have to fix.” More

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      in Theater

      Neil Marcus, Whose Art Illuminated Disability, Dies at 67

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      A playwright and actor, he saw his life as performance art. He was best known for his play “Storm Reading.”At each performance of his play “Storm Reading,” the writer and actor Neil Marcus offered his audience a reminder: “Disability is not a brave struggle or courage in the face of adversity. Disability is an art. It’s an ingenious way to live.”Mr. Marcus, who had dystonia, a neurological disorder that causes involuntary muscle contractions and affects speech, starred in the play, which comically illuminated how he passed through the world in a typical week, through vignettes of him conversing with grocery shoppers, doctors and passers-by.In 1988, when the show had its premiere at the Lobero Theater in Santa Barbara, Calif., people more often than not looked away from those with disabilities. “We’ve always been taught as kids we don’t point, don’t laugh, just basically ignore them,” Rod Lathim, the director of “Storm Reading,” said in an interview.In contrast, “Storm Reading” encouraged audiences to laugh with Mr. Marcus about his experiences.“Neil invited and welcomed, and in some cases demanded that people look,” Mr. Lathim said. “And so he brought them into his reality, which was not a reality of disability; it was a reality of his definition of life.”The success and longevity of the play, which toured throughout the country until 1996, turned Mr. Marcus into a pioneer of the disability culture movement. He called his work a reclamation of personhood in a world determined to deny people with disabilities their autonomy.Mr. Marcus died on Nov. 17 at his home in Berkeley, Calif. He was 67.His sister Kendra Marcus said the cause was dystonia.In 1987, Mr. Marcus and his brother Roger contacted Mr. Lathim, the director of Access Theater, a Santa Barbara company that regularly mounted plays featuring disabled artists. Neil Marcus sent over samples of his writing and asked Mr. Lathim if the theater would be interested in adapting them.Their conversation led to the genesis of “Storm Reading.” Mr. Marcus, his brother and Mr. Lathim worked together to draft the play, whose cast of three originally also included Roger as “The Voice,” who portrayed Neil’s thoughts during his interactions (the role was later played by Matthew Ingersoll), as well as a sign language interpreter.The show was physically taxing for Mr. Marcus. But it also invigorated him.“There’s no drug, there’s no treatment, that is, in my opinion, as powerful as the interaction between a live audience and an artist on the stage,” Mr. Lathim said. “And watching Neil transform from that was astounding.”Scenes from “Storm Reading” were filmed for NBC as part of a 1989 television special about disability, “From the Heart,” hosted by the actor Michael Douglas. The cast reunited in 2018 for a performance at the John F. Kennedy Center for the Performing Arts in Washington.Neil Marcus was born on Jan. 3, 1954, in Scarsdale, N.Y., the youngest of five children of Wil Marcus, who worked in public relations, and Lydia (Perera) Marcus, an actor. When Neil was 6, the family moved to Ojai, Calif.Neil was 8 when he learned he had dystonia, and he attempted suicide at 14 after a taxing series of surgeries, he said in a 2006 oral history interview for the Bancroft Library at the University of California, Berkeley.But counseling gave him confidence. He attended Ojai Valley School, where he was often spotted zooming around in a golf cart. After graduating from high school as valedictorian in 1971, he traveled to Laos; when he returned, he hitchhiked around the West Coast and eventually took classes at Fairhaven College, part of Western Washington University, and elsewhere. He moved to Berkeley in 1980 and became active in the disability activist community there.He explored art through various partnerships. With professional dancers, he participated in “contact improvisation” performances, which eschewed formal choreography and instead followed the seemingly frenetic movements of Mr. Marcus’s dystonia.He also wrote widely. He worked with the University of Michigan professor and activist Petra Kuppers on the Olimpias Performance Research Project, an artist collective that spotlights performers with disabilities in performances and documentaries. Their conversations on disability as art were published in a 2009 essay, “Research in Drama Education: The Journal of Applied Theatre and Performance.” The two also wrote a book, “Cripple Poetics: A Love Story” (2008), which features poetry and photography highlighting the physicality and sensuality of disability.The Neil Marcus Papers, including his essays, poems and correspondence, are held at the Bancroft Library.In addition to his sister Kendra, Mr. Marcus is survived by another sister, Wendy Marcus, and his brothers, Roger and Russell.In 2014 the Smithsonian National Museum of American History commissioned Mr. Marcus to write a poem dedicating its online exhibition “EveryBody: An Artifact History of Disability in America.”His poem began: “If there was a country called disabled, I would be from there./I live disabled culture, eat disabled food, make disabled love,/cry disabled tears, climb disabled mountains and tell disabled stories.” More

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      in Movies

      AMC to Add Onscreen Captions at Some Locations

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      The move was lauded by advocates for the deaf and the hard of hearing, but theater owners worry audiences don’t want captions.AMC Entertainment, the largest movie theater chain in the world, will offer open captioning at 240 locations in the United States, a move that the company’s chief executive described as “a real advance for those with hearing difficulties or where English is a second language.”Movie theaters provide closed captioning through devices that some customers describe as inconvenient and prone to malfunctioning. Open captions, however, are displayed on the screen in a way similar to subtitles; everyone in the theater sees the same captions, on the same screen.Advocates for the deaf and hard of hearing have long sought more and higher-quality captioning, but theater owners worry that people who aren’t deaf simply don’t like seeing captions at the movies.“In some cases, putting open captions on the screen diminishes ticket sales for the movie,” said John Fithian, the president and chief executive of the National Association of Theatre Owners, although he noted that the evidence was mostly anecdotal. He said the industry, whose business has been battered by the pandemic, was studying the relationship between open captions and ticket sales.Christian Vogler, a professor at Gallaudet University, a school in Washington that serves the deaf, said in an email, “Detractors of open captions often have argued that the wider hearing audience would revolt over them, or that these would be a losing business proposition for theaters.” He praised AMC’s move, which was announced last week, saying, “The fact that a large national chain has had a change of heart is significant, and may even open the floodgates for others to follow suit.”Other major theater chains, including Regal Cinemas and Cinemark, did not respond to messages seeking comment, and AMC did not say what precipitated the company’s decision.But Mr. Fithian, whose group represents large chains and small theater owners alike, said the industry had been paying more attention to open captioning recently as advocates for the deaf and hard of hearing have voiced concerns about closed-captioning devices.“AMC’s the first to go public with what they’re rolling out,” he said. “But this is all part of an industrywide effort to improve access by both making sure our closed-captioning systems are working, but also by expanding the number of voluntary open-caption shows across the country.”The announcement brought some measure of hope to the deaf and the hard of hearing.Megan Albertz, of South Florida, was at a brewery on Saturday where a captioned version of the 1995 Robin Williams movie “Jumanji” was playing in the background.Ms. Albertz, 29, was born with profound hearing loss and realized, having previously seen “Jumanji” without captions, that she had originally misunderstood scenes or characters’ dialogue.“Over the years, I’ve rewatched movies I had seen in theaters on various streaming platforms with captions, and I am continuously blown away with how much language or lines I missed,” she said in an email.She called AMC’s decision a step toward “accessibility for all” but wanted the company and the industry to continue expanding open-caption options.In recent years, because of litigation, legislation and pressure from disability-rights advocates, the theater industry has made closed-captioning equipment more widely available. That equipment includes the Sony glasses used by Regal Cinemas and the Captiview device, which attaches to a theater seat’s cupholder and displays captions.“These devices have their fans,” Dr. Vogler, of Gallaudet University, said, “but are also widely despised, due to both their propensity to cut out, get misconfigured, run out of battery, and their inferior usability and ergonomics compared to” open captioning.AMC said that only select, clearly designated showtimes would feature open captioning and that the “vast majority” of its showtimes would still be offered with closed captioning.The company’s chief executive, Adam Aron, noted that the expansion was in time for Marvel’s “Eternals,” which is set to open on Nov. 5 and features Lauren Ridloff, an actress who has been deaf since birth and who plays the first deaf superhero in the Marvel Cinematic Universe.In an interview with The New York Times in August, Ms. Ridloff said most movie theaters were not accessible to the deaf, who are often viewed as an “afterthought.”“You have to use a special closed-captioning device to watch subtitling in a theater, and it’s a headache, because most of the time the devices don’t work,” she said. “Then you have to go back to the front desk and find somebody to help, and by the time they figure it out that it’s not working — that it’s not going to be subtitled at all — the movie’s halfway done.” More

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      Jillian Mercado on ‘Generation Q’ and the Importance of Joyful Stories

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      This interview contains minor spoilers for Episode 9 of Season 2 of “The L Word: Generation Q.”In its five years on air, “The L Word” brought lesbian romances, drama and many, many sex scenes to the small screen. (One hundred eleven, to be exact, but who’s counting?)But Jillian Mercado — the 34-year-old actress and model who plays Maribel in the show’s reboot, “Generation Q” — never thought she would be in one of those sex scenes. Growing up with muscular dystrophy, she rarely saw physically disabled actors on TV at all.A Dominican American Bronx native who attended New York’s Fashion Institute of Technology, Mercado began making her name as a model back in 2014, when she landed her first ad campaign with Diesel. Since then, she has signed with Creative Artists Agency; founded an initiative called Black Disabled Creatives; and joined the cast of “Generation Q,” her first acting role.Although the original “L Word” notably lacked major characters who weren’t cisgender lesbians (or really anyone who fell outside of the narrow scope of straight, white beauty standards), the reboot, which debuted in late 2019, welcomed Mercado into a notably more diverse cast. And this season, as a romance blossomed between Maribel and Micah (Leo Sheng), Mercado got to become the kind of character she wanted to see when she was younger.Mercado began making her name as a model in 2014, when she landed her first ad campaign with Diesel. Her character on “Generation Q” is her first major acting role.Bethany Mollenkof for The New York Times“Intimacy and sex for the disability community was never something I literally ever saw on TV until now,” Mercado, who uses a wheelchair, wrote last month on Instagram after her first sex scene aired in Episode 5. “My heart is so FULL of gratitude that I am able to say that I am one of the first people to show you how that looks like on national television, for millions of people to see.”In the show, Mercado plays a sharp-witted lawyer who often acts as the voice of reason, doling out advice to her younger sister, Sophie, along with their mutual friends. But a more vulnerable side of her character is revealed when Maribel’s friendship with Micah, a transgender man, grows into something more complicated. As Maribel and Micah sleep together and ultimately fall in love, it gives viewers an opportunity to celebrate the two characters’ joy rather than highlight their past traumas.“Honestly, the only thing that we want is for people to understand that we’re human,” Mercado said.In a video interview from Los Angeles, where “Generation Q” is filmed, Mercado discussed queer dating and the importance of telling joyful stories about disabled people. These are edited excerpts from the conversation.Were you a fan of the original series?I actually used to watch it under my covers when I was younger because my parents thought it was a little too risqué for me to watch, which got me even more curious.Did you identify with any of the characters?I don’t think there was a specific person that I identified with. I picked parts of every character. I mean, Shane was always such a badass; she was a troublemaker. Her plots were always so chaotic and interesting.I come from a Dominican household, and we love drama. We love mixing things up. So I always leaned more toward her character. But I think that everyone just had a different aspect of what life is about. Each character highlighted the best and the worst qualities of the human experience in the dating world, and specifically the queer world.Do you think the show has done a good job deepening its representation of characters who aren’t white cisgender lesbians?I mean, I’m on the show, so that says a lot! There’s not one specific way to be queer, and that’s why “Generation Q” has been making sure that everyone is seen and heard.How did you incorporate your experiences as a queer, Hispanic person with muscular dystrophy into Maribel’s character while also being sensitive to your own boundaries and privacy?My character — and my work in general — always feeds into my real life and my personal life. But what I’ve learned, as I enter the adult world, is to really make sure that you do take time for yourself and make sure you’re aligned with what you believe in. But I also love being an advocate for my community, and I’ve been privileged to talk in my work about different things that have been lacking in my community.You’ve mentioned before that seeing Aimee Mullins open Alexander McQueen’s spring 1999 show in custom wooden prosthetic legs was formative for you as an aspiring model; were there any actors on the big or small screen who gave you a similar moment of inspiration?I think the only representation where there was with someone who had a physical disability was always in a hospital. It was always very medical, like, “Save this person from whatever their disability is.” But we’re not just all about medical devices or medical situations. We’re so much more than that. And on television, if there was representation, it was always played by somebody who didn’t have a disability. And their narration of what I was watching was not even remotely close to my lived experience or to what most disabled people live.Episode 5 of Season 2, which aired in September, contained an intimate scene between Mercado’s character, Maribel, and Micah, a transgender man played by Leo Sheng.Liz Morris/ShowtimeMaribel’s sex scene with Micah is one of few TV sex scenes involving a physically disabled person; what felt important to keep in mind as that scene was developed?The writers of the show were amazing and so communicative about what would make me feel comfortable and what was most important for me. But I know that I have never seen a sex scene with someone who is actually disabled, onscreen. And I was excited because I was like, ‘Oh, I get to do this for millions of people who’ve never seen it.’ But it also kind of hurt me that that was a reality.Yeah, it’s hot, and of course it’s “The L Word,” so everything looks amazing and beautiful, but for me, it was so much more than that. It was having the conversation that is such a taboo for people who have disabilities, where people think that we don’t go out; we don’t have relationships; we don’t have intimacy with anybody, because they think that nobody will ever love us because we look different or we live life differently. We all have different ways of being intimate with each other, and just because ours is more visibly different, it doesn’t make it less-than.“I think the only representation where there was with someone who had a physical disability was always in a hospital,” Mercado said of onscreen depictions growing up. “We’re so much more than that.”Bethany Mollenkof for The New York TimesMaribel’s relationship doesn’t blossom without friction, but her romantic plotline is notably healthy and positive this season. Why do you think the writers went in that direction with Maribel, as opposed to the complicated (and sometimes very messy) relationships that the show usually creates?It’s really special to have a story line where it’s not messy and not chaotic — because trust me, I love a good chaotic moment, but I’m a sucker for a love story. I’m such a hopeless romantic. I also think that because Leo is trans and I’m disabled, that’s already a story line in itself. People can just feel like these are just two people who really love themselves, and it doesn’t have to be messy because maybe society views them as messy.What would you like to see next for your character?Maribel is such a strong, boss character, so I’m curious to see where she goes because this is the first time that she’s really let her guard down. She’s been hurt so many times. But she’s such a stubborn, determined person that I’m curious to see if she’s going to be the one to mess it up. I know Micah is the sweetest character on this show, so there’s no way that he’s going to do anything like mess that up. But I feel like Maribel might. More