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Special Education Law: Rothstein, Special Education Law, Fourth Edition + Osborne, Special Education And The Law: A Guide For Practitioners, Second Edition
by Scott F. Johnson Professor Laura F. RothsteinSpecial Education Law 6e, written by Laura Rothstein and Scott F. Johnson, provides a comprehensive and current overview of the major federal law, and judicial interpretations of those laws, that apply to special education students. School administrators and attorneys attend to special education issues on a regular basis, and local superintendents, principals, special education professionals, psychologists, and regional and state administrators must also be familiar with the legal requirements of educating students with disabilities. Classroom teachers in all types of classrooms need to be aware of the laws that affect them and their students. Special Education Law 6e is intended for students in education and educational administration, both graduate and undergraduate, as well as law students in courses on special education law, school law, and special education. The framework of this book begins with five introductory chapters on the major issues that are addressed in special education law. These topics include an overview the legal system, the history of special education, major statutes in special education law, stakeholders such as students, families, educators, and advocates, and finally, requirements for protection under various special education laws. The remainder of the text presents and analyzes special education case law within specific contexts. The text helps educators understand what the law requires so that they can make decisions that comply with these laws. Updates for the sixth edition include a major reorganization of the text. Chapters have been streamlined and edited for clarity, combining a previous chapter on Related Services with Free Appropriate Publication Education, and folding Eligibility into Identification, Evaluation, and Eligibility, so students can better see the connections between these topics. Many case excerpts have been shortened or summarized to provide students with a more straightforward and focused reading experience. The latest updates in statutes, regulations, and case law are included throughout the text.
Special Education Law: Rothstein, Special Education Law, Fourth Edition + Osborne, Special Education And The Law: A Guide For Practitioners, Second Edition
by Scott F. Johnson Professor Laura F. RothsteinSpecial Education Law 6e, written by Laura Rothstein and Scott F. Johnson, provides a comprehensive and current overview of the major federal law, and judicial interpretations of those laws, that apply to special education students. School administrators and attorneys attend to special education issues on a regular basis, and local superintendents, principals, special education professionals, psychologists, and regional and state administrators must also be familiar with the legal requirements of educating students with disabilities. Classroom teachers in all types of classrooms need to be aware of the laws that affect them and their students. Special Education Law 6e is intended for students in education and educational administration, both graduate and undergraduate, as well as law students in courses on special education law, school law, and special education. The framework of this book begins with five introductory chapters on the major issues that are addressed in special education law. These topics include an overview the legal system, the history of special education, major statutes in special education law, stakeholders such as students, families, educators, and advocates, and finally, requirements for protection under various special education laws. The remainder of the text presents and analyzes special education case law within specific contexts. The text helps educators understand what the law requires so that they can make decisions that comply with these laws. Updates for the sixth edition include a major reorganization of the text. Chapters have been streamlined and edited for clarity, combining a previous chapter on Related Services with Free Appropriate Publication Education, and folding Eligibility into Identification, Evaluation, and Eligibility, so students can better see the connections between these topics. Many case excerpts have been shortened or summarized to provide students with a more straightforward and focused reading experience. The latest updates in statutes, regulations, and case law are included throughout the text.
Leading Equity-Based MTSS for All Students
by Amy McCart Dr. Dawn Dee MillerEnsure that Every Child Achieves Academic and Social Success An equity-based multi-tiered system of support (MTSS) helps school teams engage all students across the full range of learning needs. MTSS ensures that the vision of equity for every student is achieved, with high expectations and quality instruction, while not straining a school&’s budget or personnel. This strategy filled book teaches you how to • Engage all students in learning through an equity-based approach • Analyze and utilize your resources • Apply strengths- and evidence-based principles for implementation • Incorporate effective tools to systematize MTSS
Leading Equity-Based MTSS for All Students
by Amy McCart Dr. Dawn Dee MillerEnsure that Every Child Achieves Academic and Social Success An equity-based multi-tiered system of support (MTSS) helps school teams engage all students across the full range of learning needs. MTSS ensures that the vision of equity for every student is achieved, with high expectations and quality instruction, while not straining a school&’s budget or personnel. This strategy filled book teaches you how to • Engage all students in learning through an equity-based approach • Analyze and utilize your resources • Apply strengths- and evidence-based principles for implementation • Incorporate effective tools to systematize MTSS
Butterflies and Second Chances: A Mom's Memoir of Love and Loss
by Annette HinesThe author recounts her struggles and joys as the single mother of two daughters, one of whom has severe multiple disabilities. Born with a mitochondrial disease that causes blindness, seizures, and impairments in speech as well as motor and intellectual development, Elizabeth requires many hospitalizations and intensive full-time care when she is at home. The author writes about her struggles to obtain the help she needs and how, through her life with Elizabeth, she builds a career as a disability lawyer. She writes frankly about dealing with her grief after Elizabeth's death.
We Carry Kevan: Six Friends. Three Countries. No Wheelchair.
by Kevan ChandlerKevan is just one of the guys. It's impossible to know him and not become a little more excited about life. He is an inspiring man permeated by joy, unafraid of sorrow, full of vitality and life! His sense of humor is infectious and so is his story.He grew up, he says, at "belt-buckle level" and stayed there until Kevan's beloved posse decided to leave his wheelchair at the Atlanta airport, board a plane for France, and have his friends carry him around Europe to accomplish their dream to see the world together! Kevan's beloved posse traveled to Paris, England, and Ireland where, in the climax of their adventure, they scale 600 feet up to the 1,400-year-old monastic fortress of Skellig Michael.In WE CARRY KEVAN the reader sits with Kevan, one head-level above everyone else for the first time in his life and enjoys camaraderie unlike anything most people ever experience. Along the way they encounter the curiosity and beauty of strangers, the human family disarmed by grace, and the constant love of God so rich and beautiful in the company of good friends. WE CARRY KEVAN displays the profound power of friendship and self-sacrifice.
Forgiving God: A Story of Faith
by Hilary YanceyA young mother's life is forever changed and her faith in God is broken when her son in diagnosed with complex physical disabilities. Restore and grow your faith as you read about Hilary Yancey's personal journey back to God. Three months into her pregnancy with her first child, Hilary Yancey received a phone call that changed everything. As she learned the diagnosis-cleft lip and palate, a missing right eye, possible breathing complications-Hilary began to pray in earnest. Even in the midst of these findings, she prayed that God would heal her son. God could do a miracle unlike anything she had seen. Only when Hilary held her baby, Jack, in her arms for the first time did she realize God had given her something drastically different than what she had demanded. Hilary struggled to talk to God as she sat for six weeks beside Jack's crib in the NICU. She consented to surgeries and learned to care for a breathing tube and gastronomy button. In her experience with motherhood Hilary had become more familiar with the sound of her son's heart monitor than the sound of his heartbeat. Later, during surgeries and emergency trips back to the hospital with her crying, breathless boy, Hilary reproached the stranger God had become. Jack was different. Hilary was not the mother she once imagined. God was not who Hilary knew before. But she could not let go of one certainty-she could see the image of Christ in Jack's face. Slowly, through long nights of wrestling and longer nights of silence, Hilary cut a path through her old, familiar faith to the God behind it. She discovered that it is by walking out onto the water, where the firm ground gives way, that we can find him. And meeting Jesus, who rises with his scars to proclaim new life, is never what you once imagined.
Praying for Emily: The Faith, Science, and Miracles that Saved Our Daughter
by Tom Whitehead Kari Whitehead Emily WhiteheadDiscover the incredible true story of Emily Whitehead, the first child to receive CAR-T cell treatment for her leukemia -- and learn how her family's faith journey guided them in the fight for her life.When their five-year-old daughter was diagnosed with leukemia, Tom and Kari Whitehead's world was shattered. They vowed to do whatever it took to help their daughter, and as they made decisions about how to best treat her, Tom found his faith coming to him in "whispers," guiding his decisions and keeping his hope alive, while Kari placed great faith in science and the doctors surrounding her little girl. But as Emily's condition continued to worsen, they both prayed for a miracle.Then, their miracle arrived, in the form of an experimental treatment called CAR-T cell therapy that, against all odds, saved Emily's life. Because of Emily's miraculous recovery, this treatment is now used widely to treat cancer and has gone on to save hundreds of lives and promises to help thousands more. For all the acclaim and attention this important new approach to treating cancer has received, few know the full story of all it took to make this miracle happen.In Praying for Emily, the Whiteheads share their story, recounting the belief, resilience, and support that got them through the most difficult time of their lives.
Get in the Game: Nothing Missing: You Have Everything Needed to Succeed
by Kevin AtlasBe inspired by the story of Kevin Atlas (formerly Laue), whose faith and perseverance helped him become an NCAA Division I basketball player, despite being born with only one arm.Even before entering the world, Kevin Atlas was a fighter. He should have died in childbirth, as the umbilical cord was wrapped around his neck twice, but he survived because his left arm was in the middle of it, allowing blood to flow to his brain. But since circulation was cut off in that arm, he was born with his left arm ending just below his elbow. GET IN THE GAME is Kevin's story of transformation: Moving from anger to joy. From embarrassment to confidence. From the sidelines and wishing his life was different to getting in the game and showing who he is. Kevin's arduous journey to earning a scholarship to Manhattan College in New York City and becoming the first NCAA Division I basketball player missing a limb has given him keen insights to help anyone who feels trapped and defeated by less-than-perfect circumstances, whether physical, mental, or environmental. Kevin doesn't encourage readers to simply accept and live with their challenges, hurts, and losses. He spurs them on to believe any weakness can, in reality, become the one thing that propels them to achieve their greatest potential. As Kevin has learned throughout his life, you can't win if you don't get in the game!
All Secure: A Special Operations Soldier's Fight to Survive on the Battlefield and the Homefront
by Steve Jackson Tom SatterlyOne of the most highly regarded Tier One Delta Force operators in American military history shares his war stories and personal battle with PTSD.As a senior non-commissioned officer of Delta Force, the most elite and secretive special operations unit in the U.S. military, Command Sergeant Major Tom Satterly fought some of this country's most fearsome enemies. Over the course of twenty years and thousands of missions, he's fought desperately for his life, rescued hostages, killed and captured terrorist leaders, and seen his friends maimed and killed around him. All Secure is in part Tom's journey into a world so dark and dangerous that most Americans can't contemplate its existence. It recounts what it is like to be on the front lines with one of America's most highly trained warriors. As action-packed as any fiction thriller, All Secure is an insider's view of "The Unit." Tom is a legend even among other Tier One special operators. Yet the enemy that cost him three marriages, and ruined his health physically and psychologically, existed in his brain. It nearly led him to kill himself in 2014; but for the lifeline thrown to him by an extraordinary woman it might have ended there. Instead, they took on Satterly's most important mission-saving the lives of his brothers and sisters in arms who are killing themselves at a rate of more than twenty a day. Told through Satterly's firsthand experiences, it also weaves in the reasons-the bloodshed, the deaths, the intense moments of sheer terror, the survivor's guilt, depression, and substance abuse-for his career-long battle against the most insidious enemy of all: Post Traumatic Stress. With the help of his wife, he learned that by admitting his weaknesses and faults he sets an example for other combat veterans struggling to come home.
Wheels of Courage: How Paralyzed Veterans from World War II Invented Wheelchair Sports, Fought for Disability Rights, and Inspired a Nation
by David DavisOut of the carnage of World War II comes an unforgettable tale about defying the odds and finding hope in the most harrowing of circumstances. Wheels of Courage tells the stirring story of the soldiers, sailors, and marines who were paralyzed on the battlefield during World War II-at the Battle of the Bulge, on the island of Okinawa, inside Japanese POW camps-only to return to a world unused to dealing with their traumatic injuries. Doctors considered paraplegics to be "dead-enders" and "no-hopers," with the life expectancy of about a year. Societal stigma was so ingrained that playing sports was considered out-of-bounds for so-called "crippled bodies." But servicemen like Johnny Winterholler, a standout athlete from Wyoming before he was captured on Corregidor, and Stan Den Adel, shot in the back just days before the peace treaty ending the war was signed, refused to waste away in their hospital beds. Thanks to medical advances and the dedication of innovative physicians and rehabilitation coaches, they asserted their right to a life without limitations. The paralyzed veterans formed the first wheelchair basketball teams, and soon the Rolling Devils, the Flying Wheels, and the Gizz Kids were barnstorming the nation and filling arenas with cheering, incredulous fans. The wounded-warriors-turned-playmakers were joined by their British counterparts, led by the indomitable Dr. Ludwig Guttmann. Together, they triggered the birth of the Paralympic Games and opened the gymnasium doors to those with other disabilities, including survivors of the polio epidemic in the 1950s. Much as Jackie Robinson's breakthrough into the major leagues served as an opening salvo in the civil rights movement, these athletes helped jump-start a global movement about human adaptability. Their unlikely heroics on the court showed the world that it is ability, not disability, that matters most. Off the court, their push for equal rights led to dramatic changes in how civilized societies treat individuals with disabilities: from kneeling buses and curb cutouts to the Americans with Disabilities Act of 1990. Their saga is yet another lasting legacy of the Greatest Generation, one that has been long overlooked. Drawing on the veterans' own words, stories, and memories about this pioneering era, David Davis has crafted a narrative of survival, resilience, and triumph for sports fans and athletes, history buffs and military veterans, and people with and without disabilities.
Deer Run Home
by Ann Clare LeZotteEffie is Deaf, and no one in her family speaks sign language, her language. This moving story of survival and found family, inspired by a true court case, is perfect for fans of Wonder and Out of My Mind.* "Quietly extraordinary." -Kirkus Reviews, starred review* "Elegantly weaves a heartbreaking story with hope." -School Library Journal, starred reviewEffie and her older sister, Deja, have recently moved into their father's trailer after an incident at their mom's house. Daddy communicates with Effie by pointing, stomping on the floor, and making thoughtless jokes. Even if they did understand each other, could she tell the terrible secret she carries when telling feels impossible-and dangerous?But what if telling is the only way to be seen?This tender, spare, emotionally charged story about the impact of abuse and the power of love explores what it feels like to be an outsider in your own family and to awaken-through friendship, writing, and kinship with the natural world-to a new understanding and appreciation of yourself.
Snoop
by Gordon KormanFrom Gordon Korman, the bestselling author of Restart, the story of a boy who's stuck at home with two broken legs... and who starts using cameras and a drone to spy on his classmates, neighbors, and a possible criminal who's come to town.If Carter hadn't been checking his phone, he might have seen his brother coming down the ski slopes in his direction. And if Carter had seen his brother in time and avoided the crash, he might not have two broken legs right now.Oops.Now Carter is stuck at home for weeks, with both his legs in casts. Bored, he starts checking out the live feeds from police cams around his town. Before he knows it, he's obsessed -- watching his classmates when they don't know he's looking, and discovering some other VERY STRANGE things going on that no one else is noticing.But what happens when Carter is found out... and the people he's watching know where he lives?
Sally's Story (The Dodo)
by Bonnie BaderThe true story of how one little puppy learned to breathe on her own -- as seen on The Dodo!When Sally was rescued, this tiny dachshund puppy couldn't eat or breathe without help. Sally had a feeding tube to give her food and medicine. And she had to stay inside a plastic bubble to get the extra oxygen she needed.But Sally was determined to breathe on her own. She practiced spending small amounts of time outside her bubble. Slowly but surely, Sally's lungs grew healthy and strong. With the love and support of those around her, Sally showed the world what it means to never give up!This story is perfect for middle-grade readers and includes eight-pages of full-color photos!
Across Two Novembers: A Year in the Life of a Blind Bibliophile
by David Faucheux<P>Friends and family. Restaurants and recipes. Hobbies and history. TV programs the author loved when he could still see and music he enjoys. The schools he attended and the two degrees he attained. The career that eluded him and the physical problems that challenge him. And books, books, books: over 230 of them quoted from or reviewed. All in all, an astonishing work of erudition and remembrance.
Perché Mia Figlia Non Parla? Storia del viaggio di una madre
by Lisa Chen Sabrina AntonioliQuesto libro è basato su una storia vera ed è un'opera di saggistica creativa. Gli eventi rappresentati sono reali ma in alcuni casi sono stati romanzati per una resa efficace, o minimizzati per proteggere le persone direttamente coinvolte. Inoltre, i nomi e le caratteristiche identificative sono stati modificati per proteggere la privacy delle persone. Sebbene l'autore e l'editore abbiano compiuto ogni sforzo per garantire che le informazioni contenute in questo libro fossero corrette al momento della stampa, l'autore e l'editore con la presente non si assumono, e con la presente declinano, ogni responsabilità nei confronti di terzi per eventuali perdite, danni o interruzioni causate da errori o omissioni, se tali errori o omissioni derivano da negligenza, incidente o altre cause. Le informazioni contenute all'interno di questo e-book hanno soltanto finalità informative generali. Questo libro non è da intendersi quale sostituto di consulenza medica da parte di medici, di esperti e di terapisti. Il lettore dovrebbe consultare regolarmente un medico per le questioni riguardanti il/la proprio/a figlio/a, con particolare attenzione a tutti i sintomi che potrebbero richiedere una diagnosi o un'assistenza medica. Nessuna parte di questo libro può essere riprodotta o trasmessa in alcuna forma, o con alcun mezzo, elettronico o meccanico, incluso fotocopie, registrazioni o sistemi di salvataggio e di recupero di informazioni, senza il permesso scritto dell'autore. Copyright © 2017 di Lisa Chen Tutti i diritti riservati.
¿Por qué mi hijo no habla?
by Lisa Chen Facundo AgüeroEsta historia está basada en hechos reales y es una obra creativa de no ficción. Los sucesos relatados son reales pero en algunos casos se han modificado para darle más efecto o se han minimizado para proteger a las personas involucradas de forma directa. A pesar de que el autor y la editorial han hecho lo posible para asegurarse de que la información de este libro sea correcta a la hora de imprimirlo, el autor y la editorial no se hacen responsables y por la presente se desligan de toda responsabilidad por pérdida, daño o alteración causados por errores u omisiones, ya sea que los errores u omisiones sean consecuencia de negligencia, accidente o cualquier otra causa. La información que contiene este libro digital es únicamente para fines informativos generales. La intención de este libro no es reemplazar el consejo profesional de médicos, expertos y/o terapeutas. El lector debería, con regularidad, consultar con un médico por temas relacionados con su hijo/a y en particular con respecto a síntomas que puedan requerir un diagnóstico o atención médica. Ninguna parte de este libro digital podrá ser duplicada o transmitida de ninguna manera o por ningún medio, ya sea electrónico o mecánico, incluyendo fotocopia, grabación o por ningún sistema de almacenamiento de información o de recuperación sin el consentimiento escrito del autor.
Por que meu filho ainda não fala?
by Lisa Chen Ana Paula NascimentoTodas as crianças se desenvolvem de maneira diferente e no seu próprio ritmo. Mas e se a criança tiver dois ou três anos e ainda não falar? E se todo mundo disser para não se preocupar que a criança falaria quando estivesse pronta? Lisa Chen passou por esse exato problema com sua filha. Ao redor, todos lhe davam uma opinião diferente mas ela seguiu o conselho de um profissional e conseguiu a ajuda que precisava. O desejo de Lisa agora é permitir que pais e famílias que passam pelo mesmo problema que sua filha, encontrem ajuda cedo para assim, ajudar mais crianças. No entanto, nem toda criança terá os mesmos sintomas ou resultados que a filha de Lisa teve. Lisa escreveu este livro apenas para fins informativos. Por favor, obtenha assistência médica e profissional para opiniões sobre a saúde e o bem-estar dos seus entes queridos.
Un desiderio per te (Secondo Libro della serie "Trenta Desideri" #2)
by Elizabeth LangstonLei è una ragazza che non riesce a ricordare. Lui è il ragazzo che non riesce a dimenticare. È il suo ultimo semestre al liceo e Kimberley Rey è curiosa di scoprire cosa succederà dopo. Deve scegliere un’università, ma i suoi problemi di memoria complicano la scelta. I suoi sforzi per ricordare le renderanno impossibile lasciare casa? L'aiuto arriva attraverso un regalo inaspettato e soprannaturale. Grant è un “genio” con delle regole. Può donarle trenta desideri (uno al giorno per un mese), a patto che siano umanamente possibili. Kimberley sa bene cosa chiedere: lezioni per imparare a vivere contando solo su di sé. Ma i suoi desideri cambiano quando un suo amico riceverà una diagnosi devastante. Unendo le forze con Grant per aiutare il suo amico, Kimberley imparerà che la capacità di vivere nel momento – la capacità di dimenticare – forse può essere più preziosa di quanto potesse immaginare.v
Cam Tait
by Jim Taylor Cam Tait"I have cerebral palsy much like I have blue eyes and have-or should I say had?-brown hair. It is simply a part of who I am. When I speak to groups about my situation I can even joke about it. 'Think of CP as Canada Post,' I tell them. 'My brain sends out signals, and God knows where they wind up.'" Long-time journalist Cam Tait has seen some interesting times on the sports beat-rolling alongside Rick Hansen in the Man in Motion tour, playing in fundraising golf tournaments, and tipping back some cold ones with Wayne Gretzky, to name a few. His personal life hasn't lacked excitement either-memorable moments include parasailing, winning a stand-up (or in his case, sit-down) comedy contest, and helping his grandson take his first steps. But he couldn't have done it without the help of his friends. Tait was born with cerebral palsy, unable to sit up, speak or move his arms and legs. But thanks to a revolutionary form of physical therapy that required a 24/7 commitment from his parents and a team of 116 volunteers, he learned to get around in a wheelchair, move his hands and talk. These turned out to be useful skills for a career of prime interviews, crazy deadlines and pranks. Tait teams up with friend and fellow journalist Jim Taylor, telling his own story with characteristic directness and humour. With a newspaperman's inveterate sense of timing, Tait moves seamlessly from one-liners and tales of debauched hijinks to candid accounts of his depression, career struggles and loss of loved ones. He speaks with eloquence about the importance of giving disabled people the chance to pursue their ambitions, and the value of all the support he's received in achieving his own dreams. In both his career and personal life, he's experienced the power of humour to break down barriers and bring people together-and have a hell of a good time doing it.
Racing Fear (SideStreets #1)
by Jacqueline Guest"Racing Fear" is an action-packed ride that takes a hard look at the selling of prescription drugs.
A Screaming Kind of Day
by Rachna Gilmore"I go to my room and bang the door shut. The rain skips and dances. It's leaping down, calling me. I can hear it, I really can, Scully, Scully, Scully, a kind of rushing, roaring. I stick my head out the door and peer around. Mom's in the living room, on the couch, surrounded by her books. I duck down low and sneak out the back door, grabbing my rain coat off the hook. I tie the hood down tight so my hearing aids won't get wet. ..." Every child has had a day like this! Other books by this author are available in this library.
Chill
by Colin FrizzellHow far will Chill and Sean go to expose a teacher's deception? (Orca Soundings)
Care Work: Dreaming Disability Justice
by Leah Lakshmi Piepzna-Samarasinha<p>In their new, long-awaited collection of essays, Lambda Literary Award-winning writer and longtime disability justice activist and performance artist Leah Lakshmi Piepzna-Samarasinha explores the politics and realities of disability justice, a movement that centres the lives and leadership of sick and disabled queer, trans, Black, and brown people, with knowledge and gifts for all. Leah writes passionately and personally about creating spaces by and for sick and disabled queer people of colour, and creative "collective access" -- access not as a chore but as a collective responsibility and pleasure -- in our communities and political movements. Bringing their survival skills and knowledge from years of cultural and activist work, Piepzna-Samarasinha explores everything from the economics of queer femme emotional labour, to suicide in queer and trans communities, to the nitty-gritty of touring as a sick and disabled queer artist of colour. <p>Care Work is a mapping of access as radical love, a celebration of the work that sick and disabled queer/people of colour are doing to find each other and to build power and community, and a toolkit for everyone who wants to build radically resilient, sustainable communities of liberation where no one is left behind. Powerful and passionate, Care Work is a crucial and necessary call to arms.</p>
The Future Is Disabled: Prophecies, Love Notes and Mourning Songs
by Leah Lakshmi Piepzna-SamarasinhaIn this book, Leah Lakshmi Piepzna-Samarasinha asks some provocative questions: What if, in the near future, the majority of people will be disabled—and what if that's not a bad thing? And what if disability justice and disabled wisdom are crucial to creating a future in which it's possible to survive fascism, climate change, and pandemics and to bring about liberation? Building on the work of her game-changing book Care Work: Dreaming Disability Justice, Piepzna-Samarasinha writes about disability justice at the end of the world, documenting the many ways disabled people kept and are keeping each other—and the rest of the world—alive during Trump, fascism and the COVID-19 pandemic. Other subjects include crip interdependence, care and mutual aid in real life, disabled community building, and disabled art practice as survival and joy. Written over the course of two years of disabled isolation during the pandemic, this is a book of love letters to other disabled QTBIPOC (and those concerned about disability justice, the care crisis, and surviving the apocalypse); honor songs for kin who are gone; recipes for survival; questions and real talk about care, organizing, disabled families, and kin networks and communities; and wild brown disabled femme joy in the face of death. With passion and power, The Future Is Disabled remembers our dead and insists on our future. This updated edition includes a new chapter and afterword by the author.