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"bio": "\u003ca href=\"http://www.MarkFiore.com\">MarkFiore.com\u003c/a> | \u003ca href=\"https://twitter.com/markfiore\">Follow on Twitter\u003c/a> | \u003ca href=\"https://www.facebook.com/pages/Mark-Fiore-Animated-Political-Cartoons/94451707396?ref=bookmarks\">Facebook\u003c/a> | \u003ca href=\"mailto:mark@markfiore.com\">email\u003c/a>\r\n\r\nPulitzer Prize-winner, Mark Fiore, who the Wall Street Journal has called “the undisputed guru of the form,” creates animated political cartoons in San Francisco, where his work has been featured regularly on the San Francisco Chronicle’s web site, SFGate.com. His work has appeared on Newsweek.com, Slate.com, CBSNews.com, MotherJones.com, DailyKos.com and NPR’s web site. Fiore’s political animation has appeared on CNN, Frontline, Bill Moyers Journal, Salon.com and cable and broadcast outlets across the globe.\r\n\r\nBeginning his professional life by drawing traditional political cartoons for newspapers, Fiore’s work appeared in publications ranging from the Washington Post to the Los Angeles Times. In the late 1990s, he began to experiment with animating political cartoons and, after a short stint at the San Jose Mercury News as their staff cartoonist, Fiore devoted all his energies to animation.\r\nGrowing up in California, Fiore also spent a good portion of his life in the backwoods of Idaho. It was this combination that shaped him politically. Mark majored in political science at Colorado College, where, in a perfect send-off for a cartoonist, he received his diploma in 1991 as commencement speaker Dick Cheney smiled approvingly.\r\nMark Fiore was awarded the Pulitzer Prize for political cartooning in 2010, a Robert F. Kennedy Journalism Award in 2004 and has twice received an Online Journalism Award for commentary from the Online News Association (2002, 2008). Fiore has received two awards for his work in new media from the National Cartoonists Society (2001, 2002), and in 2006 received The James Madison Freedom of Information Award from The Society of Professional Journalists.",
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"content": "\u003cp style=\"text-align: left\">A Concord woman with a life threatening condition who fought successfully to regain humanitarian protections for sick immigrants will attend President Trump’s State of the Union address next week.\u003c/p>\n\u003cp>[pullquote size='medium' align='right' citation=\"Karla Bueso, Maria Isabel's mother\"]‘It’s such an honor for Maria Isabel. That girl has gone through some very difficult times, but she’s also getting to live some pretty exceptional moments.’[/pullquote]\u003c/p>\n\u003cp>Maria Isabel Bueso, 24, became a public face of the plight of hundreds of immigrants who faced deportation last year after the Trump administration abruptly stopped issuing the temporary relief waivers they had relied on to stay in the United States and continue receiving medical treatment.\u003c/p>\n\u003cp>Bueso, who was born in Guatemala with a rare genetic disease, \u003ca href=\"https://www.kqed.org/news/11798764/bernie-sanders-pulls-away-from-pack-in-california\" target=\"_blank\" rel=\"noopener noreferrer\">testified at a congressional hearing\u003c/a> in September, insisting she would die if she were deported. National media outlets covered her story, and public outcry intensified.\u003c/p>\n\u003cp>Shortly after, U.S. Citizenship and Immigration Services reversed its position and resumed considering requests for so-called medical deferred action. In December, the agency \u003ca href=\"https://www.kqed.org/news/11790433/concord-woman-with-rare-disease-granted-reprieve-from-deportation\" target=\"_blank\" rel=\"noopener noreferrer\">approved\u003c/a> Bueso’s request to remain in the U.S. for another two years.\u003c/p>\n\u003cp>At the State of the Union on Feb. 4, Bueso will be the guest of Rep. Mark DeSaulnier, D-Concord, who called for the congressional hearing she testified at and later \u003ca href=\"https://desaulnier.house.gov/media-center/press-releases/congressman-desaulnier-announces-private-bill-protect-maria-isabel-bueso\" target=\"_blank\" rel=\"noopener noreferrer\">introduced a House bill\u003c/a> that would grant legal permanent resident status to Bueso and her immediate family.\u003c/p>\n\u003cp>Bueso moved to the U.S. with her family when she was 7 after doctors in the Bay Area invited her to participate in a clinical trial for a new drug to treat her condition — Mucopolysaccharidosis type VI.\u003c/p>\n\u003cp>The trial led to the U.S. Food and Drug Administration’s approval of the drug, which Bueso needs to survive. She receives it through intravenous infusions at UCSF Benioff Children’s Hospital in Oakland.\u003c/p>\n\u003cp>[aside label=\"related coverage\" tag=\"maria-isabel-bueso\"]“Isabel is one of my personal heroes and she deserves to stay in this country,” DeSaulnier said in a statement. “I am proud to help lead her fight in Congress and am so pleased she is joining me for the State of the Union.”\u003c/p>\n\u003cp>The medicine is not available in Guatemala, said her doctor, Paul Harmatz, a pediatrician at the hospital who led the clinical trial.\u003c/p>\n\u003cp>The disease has left Bueso confined to a wheelchair and dependent on a device implanted in her throat to breathe. But she still excelled in school, graduating summa cum laude from Cal State University, East Bay in 2018. Bueso also became a nationally recognized advocate for people with rare genetic conditions.\u003c/p>\n\u003cp>Bueso’s mom, Karla, said she was grateful her daughter would be present at the State of the Union.\u003c/p>\n\u003cp>“It’s such an honor for Maria Isabel,” said Karla, from the family’s home in Concord. “That girl has gone through some very difficult times, but she’s also getting to live some pretty exceptional moments.”\u003cbr>\n[ad fullwidth]\u003c/p>\n\u003cp>\u003c/p>\n",
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"content": "\u003cdiv class=\"post-body\">\u003cp>“Isabel is one of my personal heroes and she deserves to stay in this country,” DeSaulnier said in a statement. “I am proud to help lead her fight in Congress and am so pleased she is joining me for the State of the Union.”\u003c/p>\n\u003cp>The medicine is not available in Guatemala, said her doctor, Paul Harmatz, a pediatrician at the hospital who led the clinical trial.\u003c/p>\n\u003cp>The disease has left Bueso confined to a wheelchair and dependent on a device implanted in her throat to breathe. But she still excelled in school, graduating summa cum laude from Cal State University, East Bay in 2018. Bueso also became a nationally recognized advocate for people with rare genetic conditions.\u003c/p>\n\u003cp>Bueso’s mom, Karla, said she was grateful her daughter would be present at the State of the Union.\u003c/p>\n\u003cp>“It’s such an honor for Maria Isabel,” said Karla, from the family’s home in Concord. “That girl has gone through some very difficult times, but she’s also getting to live some pretty exceptional moments.”\u003cbr>\n\u003c/p>\u003c/div>",
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"content": "\u003cp>A Bay Area woman receiving lifesaving treatment for a rare genetic condition, who could die if she were deported, has been approved by the federal government to remain in the U.S. for two more years.\u003c/p>\n\u003cp>The reprieve marks a reversal by the Trump administration, and comes months after immigration authorities told Concord resident Maria Isabel Bueso that she and her immediate family had 33 days to leave the country or face deportation.\u003c/p>\n\u003cp>Bueso, 24, depends on a weekly intravenous infusion of medicine at an Oakland hospital to survive. The treatment is not available in her native Guatemala.\u003c/p>\n\u003cp>In a letter drafted Dec. 6, U.S. Citizenship and Immigration Services’ San Francisco district director, John Kramar, informed Bueso that her request for humanitarian relief, known as deferred action, had been granted and is effective until Aug. 13, 2021.\u003c/p>\n\u003cp>[pullquote size='medium' align='right' citation=\"Maria Isabel Bueso\"]‘What I learned from this was to not be afraid — to speak up from your heart and to know that your voice matters.’[/pullquote]\u003c/p>\n\u003cp>“I was so happy and relieved,” Bueso said. “I really appreciate everyone who has been so kind to my family and given us support.”\u003c/p>\n\u003cp>Forcing Bueso to leave the U.S. would be akin to “pulling the plug on a respirator,” said Dr. Paul Harmatz, a pediatrician at UCSF Benioff Children’s Hospital, who treats her.\u003c/p>\n\u003cp>The genetic disease, which stunts normal skeletal development and can cause respiratory complications and organ degeneration, has left Bueso confined to a wheelchair and breathing through a device implanted in her throat.\u003c/p>\n\u003cp>Bueso came to the U.S. with her family when she was 7, after Harmatz and other doctors in the Bay Area invited her to participate in a clinical trial for a new drug to treat her condition — \u003ca href=\"https://ghr.nlm.nih.gov/condition/mucopolysaccharidosis-type-vi\" target=\"_blank\" rel=\"noopener noreferrer\">Mucopolysaccharidosis type VI\u003c/a>. Her participation in that trial was very important in order for the U.S. Food and Drug Administration to approve the drug, called Naglazyme, said Harmatz, who led the trial.\u003c/p>\n\u003cfigure id=\"attachment_11790508\" class=\"wp-caption alignnone\" style=\"max-width: 1920px\">\u003ca href=\"https://ww2.kqed.org/app/uploads/sites/10/2019/12/RS38885_IMG_1325-qut.jpg\">\u003cimg loading=\"lazy\" decoding=\"async\" class=\"wp-image-11790508 size-full\" src=\"https://ww2.kqed.org/app/uploads/sites/10/2019/12/RS38885_IMG_1325-qut.jpg\" alt=\"\" width=\"1920\" height=\"1440\" srcset=\"https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut.jpg 1920w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-160x120.jpg 160w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-800x600.jpg 800w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1020x765.jpg 1020w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1200x900.jpg 1200w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1832x1374.jpg 1832w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1376x1032.jpg 1376w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1044x783.jpg 1044w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-632x474.jpg 632w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-536x402.jpg 536w\" sizes=\"(max-width: 1920px) 100vw, 1920px\">\u003c/a>\u003cfigcaption class=\"wp-caption-text\">Maria Isabel Bueso (R) and her mother, Karla Bueso, at their attorney’s offices in San Francisco on Aug. 29, 2019. ‘I haven’t slept for days,’ said Karla at the time, out of concern that her daughter could lose vital medical treatment in the U.S. \u003ccite>(Farida Jhabvala Romero/KQED)\u003c/cite>\u003c/figcaption>\u003c/figure>\n\u003cp>Bueso and her family were subsequently able to renew their deferred action status several times. Bueso has since become a nationally renowned advocate for people with rare diseases.\u003c/p>\n\u003cp>Last year, Bueso graduated summa cum laude from CSU East Bay, where she helped create a scholarship fund for students with disabilities.\u003c/p>\n\u003cp>But in early August, USCIS stopped reviewing almost all applications for deferred action, including those of immigrants in need of medical treatment in the U.S.\u003c/p>\n\u003cp>[ad fullwidth]\u003c/p>\n\u003cp>About 700 people had pending applications for the humanitarian protection at the time, including 420 who were sent denial letters, according to agency officials who testified at \u003ca href=\"https://oversight.house.gov/legislation/hearings/the-administration-s-apparent-revocation-of-medical-deferred-action-for\" target=\"_blank\" rel=\"noopener noreferrer\">a hearing\u003c/a> of the House Committee on Oversight and Reform in September.\u003c/p>\n\u003cp>During the hearing, at which Bueso testified, USCIS officials were excoriated by several lawmakers, and public outcry grew in the following days. A week later, on Sept. 19, the agency announced it was resuming consideration of nonmilitary deferred action requests on a case-by-case basis.\u003c/p>\n\u003cp>The renewal for Bueso and her family — which includes work permits — means Bueso’s father, Alberto, can continue his job in sales at an import-export company. His employment supports the family and pays for Bueso’s medical care.\u003c/p>\n\u003cp>USCIS declined to comment on Bueso’s case.\u003c/p>\n\u003cp>[aside label=\"related coverage\" tag=\"deferred-action\"]On Monday, Rep. Mark DeSaulnier, a Democrat representing Contra Costa County who championed Bueso’s case and called for the congressional hearing, said he tepidly applauded USCIS’ decision to allow Bueso to remain in the country.\u003c/p>\n\u003cp>“This is a good first step,” he said. “We’re continuing to work on a permanent solution, but at least this can reasonably reduce our fears for two years.”\u003c/p>\n\u003cp>DeSaulnier introduced a \u003ca href=\"https://www.congress.gov/bill/116th-congress/house-bill/4225\" target=\"_blank\" rel=\"noopener noreferrer\">bill\u003c/a> in the House in late August that would grant legal permanent resident status to Bueso and her immediate family. Sens. Dianne Feinstein, D-California, and Lindsey Graham, R-South Carolina, introduced similar legislation in the Senate.\u003c/p>\n\u003cp>In collaboration with Democratic Rep. Ayanna Pressley of Massachusetts, who also has constituents affected by the halt to deferred action, DeSaulnier said he is also working on a broader proposal to provide more permanent relief to other immigrants in need of medical treatment in the U.S.\u003c/p>\n\u003cp>This fall, Bueso was recognized by both the \u003ca href=\"https://rareadvocates.org/rare-disease-legislative-advocates-honor-leaders-who-inspire-transformational-public-policy-solutions/\" target=\"_blank\" rel=\"noopener noreferrer\">Rare Disease Legislative Advocates\u003c/a> and the \u003ca href=\"https://members.eastbayleadershipcouncil.com/blog/eblc-news-updates-97/post/isabel-bueso-and-betsy-biern-to-keynote-the-philanthropy-awards-21067\" target=\"_blank\" rel=\"noopener noreferrer\">East Bay Leadership Council\u003c/a> for her work advocating for immigrants who depend on deferred action status to receive lifesaving medical treatment in the U.S.\u003c/p>\n\u003cp>Bueso said that she and her family have been living in limbo for the last six months, a period full of fear and stress. But her ordeal, she added, has also been an important learning experience.\u003c/p>\n\u003cp>“What I learned from this was to not be afraid — to speak up from your heart and to know that your voice matters,” she said.\u003c/p>\n\u003cp>\u003c/p>\n",
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"excerpt": "The Trump administration's policy reversal grants two-year deferred action protection to Guatemalan-born Maria Isabel Bueso, whose life depends on weekly medical treatments at an Oakland hospital.",
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"title": "Concord Woman With Rare Disease Granted Reprieve From Deportation | KQED",
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"content": "\u003cdiv class=\"post-body\">\u003cp>\u003cp>A Bay Area woman receiving lifesaving treatment for a rare genetic condition, who could die if she were deported, has been approved by the federal government to remain in the U.S. for two more years.\u003c/p>\n\u003cp>The reprieve marks a reversal by the Trump administration, and comes months after immigration authorities told Concord resident Maria Isabel Bueso that she and her immediate family had 33 days to leave the country or face deportation.\u003c/p>\n\u003cp>Bueso, 24, depends on a weekly intravenous infusion of medicine at an Oakland hospital to survive. The treatment is not available in her native Guatemala.\u003c/p>\n\u003cp>In a letter drafted Dec. 6, U.S. Citizenship and Immigration Services’ San Francisco district director, John Kramar, informed Bueso that her request for humanitarian relief, known as deferred action, had been granted and is effective until Aug. 13, 2021.\u003c/p>\n\u003cp>\u003c/p>\u003c/div>",
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"content": "\u003cdiv class=\"post-body\">\u003cp>\u003c/p>\n\u003cp>“I was so happy and relieved,” Bueso said. “I really appreciate everyone who has been so kind to my family and given us support.”\u003c/p>\n\u003cp>Forcing Bueso to leave the U.S. would be akin to “pulling the plug on a respirator,” said Dr. Paul Harmatz, a pediatrician at UCSF Benioff Children’s Hospital, who treats her.\u003c/p>\n\u003cp>The genetic disease, which stunts normal skeletal development and can cause respiratory complications and organ degeneration, has left Bueso confined to a wheelchair and breathing through a device implanted in her throat.\u003c/p>\n\u003cp>Bueso came to the U.S. with her family when she was 7, after Harmatz and other doctors in the Bay Area invited her to participate in a clinical trial for a new drug to treat her condition — \u003ca href=\"https://ghr.nlm.nih.gov/condition/mucopolysaccharidosis-type-vi\" target=\"_blank\" rel=\"noopener noreferrer\">Mucopolysaccharidosis type VI\u003c/a>. Her participation in that trial was very important in order for the U.S. Food and Drug Administration to approve the drug, called Naglazyme, said Harmatz, who led the trial.\u003c/p>\n\u003cfigure id=\"attachment_11790508\" class=\"wp-caption alignnone\" style=\"max-width: 1920px\">\u003ca href=\"https://ww2.kqed.org/app/uploads/sites/10/2019/12/RS38885_IMG_1325-qut.jpg\">\u003cimg loading=\"lazy\" decoding=\"async\" class=\"wp-image-11790508 size-full\" src=\"https://ww2.kqed.org/app/uploads/sites/10/2019/12/RS38885_IMG_1325-qut.jpg\" alt=\"\" width=\"1920\" height=\"1440\" srcset=\"https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut.jpg 1920w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-160x120.jpg 160w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-800x600.jpg 800w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1020x765.jpg 1020w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1200x900.jpg 1200w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1832x1374.jpg 1832w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1376x1032.jpg 1376w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-1044x783.jpg 1044w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-632x474.jpg 632w, https://cdn.kqed.org/wp-content/uploads/sites/10/2019/12/RS38885_IMG_1325-qut-536x402.jpg 536w\" sizes=\"(max-width: 1920px) 100vw, 1920px\">\u003c/a>\u003cfigcaption class=\"wp-caption-text\">Maria Isabel Bueso (R) and her mother, Karla Bueso, at their attorney’s offices in San Francisco on Aug. 29, 2019. ‘I haven’t slept for days,’ said Karla at the time, out of concern that her daughter could lose vital medical treatment in the U.S. \u003ccite>(Farida Jhabvala Romero/KQED)\u003c/cite>\u003c/figcaption>\u003c/figure>\n\u003cp>Bueso and her family were subsequently able to renew their deferred action status several times. Bueso has since become a nationally renowned advocate for people with rare diseases.\u003c/p>\n\u003cp>Last year, Bueso graduated summa cum laude from CSU East Bay, where she helped create a scholarship fund for students with disabilities.\u003c/p>\n\u003cp>But in early August, USCIS stopped reviewing almost all applications for deferred action, including those of immigrants in need of medical treatment in the U.S.\u003c/p>\n\u003cp>\u003c/p>\u003c/div>",
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"content": "\u003cdiv class=\"post-body\">\u003cp>\u003c/p>\n\u003cp>About 700 people had pending applications for the humanitarian protection at the time, including 420 who were sent denial letters, according to agency officials who testified at \u003ca href=\"https://oversight.house.gov/legislation/hearings/the-administration-s-apparent-revocation-of-medical-deferred-action-for\" target=\"_blank\" rel=\"noopener noreferrer\">a hearing\u003c/a> of the House Committee on Oversight and Reform in September.\u003c/p>\n\u003cp>During the hearing, at which Bueso testified, USCIS officials were excoriated by several lawmakers, and public outcry grew in the following days. A week later, on Sept. 19, the agency announced it was resuming consideration of nonmilitary deferred action requests on a case-by-case basis.\u003c/p>\n\u003cp>The renewal for Bueso and her family — which includes work permits — means Bueso’s father, Alberto, can continue his job in sales at an import-export company. His employment supports the family and pays for Bueso’s medical care.\u003c/p>\n\u003cp>USCIS declined to comment on Bueso’s case.\u003c/p>\n\u003cp>\u003c/p>\u003c/div>",
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"content": "\u003cdiv class=\"post-body\">\u003cp>On Monday, Rep. Mark DeSaulnier, a Democrat representing Contra Costa County who championed Bueso’s case and called for the congressional hearing, said he tepidly applauded USCIS’ decision to allow Bueso to remain in the country.\u003c/p>\n\u003cp>“This is a good first step,” he said. “We’re continuing to work on a permanent solution, but at least this can reasonably reduce our fears for two years.”\u003c/p>\n\u003cp>DeSaulnier introduced a \u003ca href=\"https://www.congress.gov/bill/116th-congress/house-bill/4225\" target=\"_blank\" rel=\"noopener noreferrer\">bill\u003c/a> in the House in late August that would grant legal permanent resident status to Bueso and her immediate family. Sens. Dianne Feinstein, D-California, and Lindsey Graham, R-South Carolina, introduced similar legislation in the Senate.\u003c/p>\n\u003cp>In collaboration with Democratic Rep. Ayanna Pressley of Massachusetts, who also has constituents affected by the halt to deferred action, DeSaulnier said he is also working on a broader proposal to provide more permanent relief to other immigrants in need of medical treatment in the U.S.\u003c/p>\n\u003cp>This fall, Bueso was recognized by both the \u003ca href=\"https://rareadvocates.org/rare-disease-legislative-advocates-honor-leaders-who-inspire-transformational-public-policy-solutions/\" target=\"_blank\" rel=\"noopener noreferrer\">Rare Disease Legislative Advocates\u003c/a> and the \u003ca href=\"https://members.eastbayleadershipcouncil.com/blog/eblc-news-updates-97/post/isabel-bueso-and-betsy-biern-to-keynote-the-philanthropy-awards-21067\" target=\"_blank\" rel=\"noopener noreferrer\">East Bay Leadership Council\u003c/a> for her work advocating for immigrants who depend on deferred action status to receive lifesaving medical treatment in the U.S.\u003c/p>\n\u003cp>Bueso said that she and her family have been living in limbo for the last six months, a period full of fear and stress. But her ordeal, she added, has also been an important learning experience.\u003c/p>\n\u003cp>“What I learned from this was to not be afraid — to speak up from your heart and to know that your voice matters,” she said.\u003c/p>\n\u003cp>\u003c/p>\n\u003c/div>\u003c/p>",
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"content": "\u003cp>Amid intense criticism and a congressional inquiry, U.S. Citizenship and Immigration Services announced Thursday it will resume processing requests for long-standing humanitarian protections that allow immigrants to receive often lifesaving medical treatment in the country.\u003c/p>\n\u003cp>The order to completely reverse the policy change by USCIS on deportation relief for medical conditions, known as medical deferred action, came from the top official at the Department of Homeland Security, a USCIS spokesperson said.\u003c/p>\n\u003cp>“At the direction of [DHS] acting Secretary McAleenan, USCIS is resuming its consideration of non-military deferred action requests on a discretionary, case-by-case basis, except as otherwise required by an applicable statute, regulation, or court order,” the spokesperson said in a statement.\u003c/p>\n\u003cp>USCIS receives about 1,000 requests for deferred action per year, mostly for family support or medical reasons.\u003c/p>\n\u003cp>Since Aug. 7, USCIS denied the protections for more than 420 immigrants, as the agency abruptly stopped considering such requests, except for military families.\u003c/p>\n\u003cp>[ad fullwidth]\u003c/p>\n\u003cp>Concord resident Maria Isabel Bueso, who was born with a rare genetic disorder and must receive weekly intravenous infusions of medicine at an Oakland hospital to survive, was told by USCIS to leave the country in 33 days or face deportation.\u003c/p>\n\u003cp>After public outcry, including \u003ca href=\"https://desaulnier.house.gov/sites/desaulnier.house.gov/files/2019-08-30%20Congressional%20Letter%20to%20USCIS%20Regarding%20Medical%20Deferred%20Action.pdf\" target=\"_blank\" rel=\"noopener\">a letter\u003c/a> signed by nearly 130 members of Congress urging USCIS to reverse the shift in policy, the agency said on Sept. 2 it would reopen pending cases only, such as Bueso’s. But the future of medical deferred action, which must be renewed every two years, remained unclear.\u003c/p>\n\u003cp>Bueso, 24, testified during a four-hour \u003ca href=\"https://oversight.house.gov/legislation/hearings/the-administration-s-apparent-revocation-of-medical-deferred-action-for\" target=\"_blank\" rel=\"noopener\">congressional hearing\u003c/a> last week that she would die if forced to leave the U.S. The medicine she currently receives is not available in her native Guatemala.\u003c/p>\n\u003cp>Daniel Renaud, associate director at USCIS’ Field Operations Directorate, refused to answer questions from outraged members of Congress about how or why the agency decided to stop considering deferred action requests, citing a recent \u003ca href=\"https://www.wbur.org/news/2019/09/05/aclu-lawsuit-medical-deferred-action\">lawsuit\u003c/a> by an immigrant rights group in Massachusetts challenging the policy change .\u003c/p>\n\u003cp>After the news Thursday, Bueso said she and her family were “cautiously optimistic.”\u003c/p>\n\u003cp>“I am so grateful to all of the leaders who spoke with me last week in D.C. and played a role in helping to reinstate the deferred action program,” Bueso said. “We now wait to see whether our case will be approved, as well as confirmation on the future of the program in order to give families like mine the assurance that our lives won’t continue to be threatened.”\u003c/p>\n\u003cp>[aside postID='news_11771386,news_11772008' label='Related Coverage']\u003c/p>\n\u003cp>Congressman Mark DeSaulnier, D-Concord, a member of the Oversight and Reform Committee who requested the hearing, said he still wants answers for Bueso, who is his constituent, and others.\u003c/p>\n\u003cp>“This will save people’s lives, but we never should have had to go through it. I’m grateful that they’ve come to their senses and we are back to where they should’ve stayed,” DeSaulnier said. “But I want to find out who was responsible and they should be held accountable to the Congress and the U.S. taxpayers. This was a waste of money. Very cruel.”\u003c/p>\n\u003cp>DeSaulnier said the oversight committee was planning a second hearing next week ordering USCIS officials to attend.\u003c/p>\n\u003cp>“I think that may be part of the reason they decided to back off,” he said.\u003c/p>\n\u003cp>Bueso was 7 years old when she moved to the U.S. with her parents and sister, after doctors at UC San Francisco invited her to participate in a clinical trial that eventually led to federal approval of a drug to treat her condition — mucopolysaccharidosis type VI.\u003c/p>\n\u003cp>Doctors in Guatemala had told Bueso’s parents she wouldn’t survive past age 10. But the medical treatment at UCSF has extended her life more than a decade.\u003c/p>\n\u003cp>The disease left her confined to a wheelchair and breathing through a device in her throat. But that didn’t stop Bueso from training to become a dance instructor and graduating summa cum laude from California State University East Bay — where she set up a scholarship fund for students with disabilities.\u003c/p>\n\u003cp>People with Bueso’s disease lack an enzyme that allows the body to break down certain sugars. The genetic mutation leads to very short stature, because the skeletal system cannot develop normally, as well as pulmonary, heart and other problems.\u003c/p>\n\u003cp>\u003c/p>\n\u003cp>DeSaulnier introduced a private bill that would grant permanent resident status — green cards — to Bueso and her family. He said he’s also working on a separate bill to protect other immigrants with significant medical needs who depend on deferred action.\u003c/p>\n\n",
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"content": "\u003cdiv class=\"post-body\">\u003cp>\u003cp>Amid intense criticism and a congressional inquiry, U.S. Citizenship and Immigration Services announced Thursday it will resume processing requests for long-standing humanitarian protections that allow immigrants to receive often lifesaving medical treatment in the country.\u003c/p>\n\u003cp>The order to completely reverse the policy change by USCIS on deportation relief for medical conditions, known as medical deferred action, came from the top official at the Department of Homeland Security, a USCIS spokesperson said.\u003c/p>\n\u003cp>“At the direction of [DHS] acting Secretary McAleenan, USCIS is resuming its consideration of non-military deferred action requests on a discretionary, case-by-case basis, except as otherwise required by an applicable statute, regulation, or court order,” the spokesperson said in a statement.\u003c/p>\n\u003cp>USCIS receives about 1,000 requests for deferred action per year, mostly for family support or medical reasons.\u003c/p>\n\u003cp>Since Aug. 7, USCIS denied the protections for more than 420 immigrants, as the agency abruptly stopped considering such requests, except for military families.\u003c/p>\n\u003cp>\u003c/p>\u003c/div>",
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"content": "\u003cdiv class=\"post-body\">\u003cp>\u003c/p>\n\u003cp>Congressman Mark DeSaulnier, D-Concord, a member of the Oversight and Reform Committee who requested the hearing, said he still wants answers for Bueso, who is his constituent, and others.\u003c/p>\n\u003cp>“This will save people’s lives, but we never should have had to go through it. I’m grateful that they’ve come to their senses and we are back to where they should’ve stayed,” DeSaulnier said. “But I want to find out who was responsible and they should be held accountable to the Congress and the U.S. taxpayers. This was a waste of money. Very cruel.”\u003c/p>\n\u003cp>DeSaulnier said the oversight committee was planning a second hearing next week ordering USCIS officials to attend.\u003c/p>\n\u003cp>“I think that may be part of the reason they decided to back off,” he said.\u003c/p>\n\u003cp>Bueso was 7 years old when she moved to the U.S. with her parents and sister, after doctors at UC San Francisco invited her to participate in a clinical trial that eventually led to federal approval of a drug to treat her condition — mucopolysaccharidosis type VI.\u003c/p>\n\u003cp>Doctors in Guatemala had told Bueso’s parents she wouldn’t survive past age 10. But the medical treatment at UCSF has extended her life more than a decade.\u003c/p>\n\u003cp>The disease left her confined to a wheelchair and breathing through a device in her throat. But that didn’t stop Bueso from training to become a dance instructor and graduating summa cum laude from California State University East Bay — where she set up a scholarship fund for students with disabilities.\u003c/p>\n\u003cp>People with Bueso’s disease lack an enzyme that allows the body to break down certain sugars. The genetic mutation leads to very short stature, because the skeletal system cannot develop normally, as well as pulmonary, heart and other problems.\u003c/p>\n\u003cp>\u003c/p>\n\u003cp>DeSaulnier introduced a private bill that would grant permanent resident status — green cards — to Bueso and her family. He said he’s also working on a separate bill to protect other immigrants with significant medical needs who depend on deferred action.\u003c/p>\n\n\u003c/div>\u003c/p>",
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"mindshift": {
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"info": "The MindShift podcast explores the innovations in education that are shaping how kids learn. Hosts Ki Sung and Katrina Schwartz introduce listeners to educators, researchers, parents and students who are developing effective ways to improve how kids learn. We cover topics like how fed-up administrators are developing surprising tactics to deal with classroom disruptions; how listening to podcasts are helping kids develop reading skills; the consequences of overparenting; and why interdisciplinary learning can engage students on all ends of the traditional achievement spectrum. This podcast is part of the MindShift education site, a division of KQED News. KQED is an NPR/PBS member station based in San Francisco. You can also visit the MindShift website for episodes and supplemental blog posts or tweet us \u003ca href=\"https://twitter.com/MindShiftKQED\">@MindShiftKQED\u003c/a> or visit us at \u003ca href=\"/mindshift\">MindShift.KQED.org\u003c/a>",
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"info": "For decades, the process for how police police themselves has been inconsistent – if not opaque. In some states, like California, these proceedings were completely hidden. After a new police transparency law unsealed scores of internal affairs files, our reporters set out to examine these cases and the shadow world of police discipline. On Our Watch brings listeners into the rooms where officers are questioned and witnesses are interrogated to find out who this system is really protecting. Is it the officers, or the public they've sworn to serve?",
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"info": "Political Breakdown is a new series that explores the political intersection of California and the nation. Each week hosts Scott Shafer and Marisa Lagos are joined with a new special guest to unpack politics -- with personality — and offer an insider’s glimpse at how politics happens.",
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"possible": {
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"info": "Possible is hosted by entrepreneur Reid Hoffman and writer Aria Finger. Together in Possible, Hoffman and Finger lead enlightening discussions about building a brighter collective future. The show features interviews with visionary guests like Trevor Noah, Sam Altman and Janette Sadik-Khan. Possible paints an optimistic portrait of the world we can create through science, policy, business, art and our shared humanity. It asks: What if everything goes right for once? How can we get there? Each episode also includes a short fiction story generated by advanced AI GPT-4, serving as a thought-provoking springboard to speculate how humanity could leverage technology for good.",
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"pri-the-world": {
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},
"radiolab": {
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"info": "A two-time Peabody Award-winner, Radiolab is an investigation told through sounds and stories, and centered around one big idea. In the Radiolab world, information sounds like music and science and culture collide. Hosted by Jad Abumrad and Robert Krulwich, the show is designed for listeners who demand skepticism, but appreciate wonder. WNYC Studios is the producer of other leading podcasts including Freakonomics Radio, Death, Sex & Money, On the Media and many more.",
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},
"reveal": {
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