Service Alert
CD service concludes July 31, 2025
CELA's audiobooks and magazines are available in Direct to Player and downloadable formats. We no longer mail out CDs. Please contact us for more information.
CELA's audiobooks and magazines are available in Direct to Player and downloadable formats. We no longer mail out CDs. Please contact us for more information.
Showing 1 - 20 of 22 items
By Alice Wong. 2024
The much-anticipated follow up to the groundbreaking anthology Disability Visibility : another revolutionary collection of first-person writing on the joys…
and challenges of the modern disability experience, and intimacy in all its myriad forms. What is intimacy? More than sex, more than romantic love, the pieces in this stunning and illuminating new anthology offer broader and more inclusive definitions of what it can mean to be intimate with another person. Explorations of caregiving, community, access, and friendship offer us alternative ways of thinking about the connections we form with others—a vital reimagining in an era when forced physical distance is at times a necessary norm. But don't worry: there's still sex to consider—and the numerous ways sexual liberation intersects with disability justice. Plunge between these pages and you'll also find disabled sexual discovery, disabled love stories, and disabled joy. These twenty-five stunning original pieces—plus other modern classics on the subject, all carefully curated by acclaimed activist Alice Wong—include essays, poetry, drama, and erotica: a full spectrum of the dreams, fantasies, and deeply personal realities of a wide range of beautiful bodies and minds. Disability Intimacy will free your thinking, invigorate your spirit, and delight your desiresBy Rod Michalko, Dan Goodley. 2023
Letters with Smokie captures an epistolic exchange between Dan Goodley and Rod Michalko, or rather, Rod Michalko's late guide dog,…
Smokie. A lively exploration of human-animal relationships and disability as disruption, disturbance, and art, the book offers a refreshing re-evaluation of cultural misunderstandings of disability.By Rod Michalko. 2024
In September 2020, Rod Michalko wrote to friend and colleague Dan Goodley, congratulating him on the release of his latest…
book, Disability and Other Human Questions . Joking that his late guide dog, Smokie, had taken offense to the suggestion that disability was purely a human question, Michalko shared a few thoughts on behalf of his dog. When Goodley wrote back—to Smokie—so began an epistolic exchange that would continue for the next seven months. As the COVID-19 pandemic swept across the world and the realities of lockdown-imposed isolation set in, the Smokie letters provided the friends a space in which to come together in a lively exploration of human-animal relationships and to interrogate disability as disruption, disturbance, and art. Just as he did in life, Smokie guides. In these pages, he offers wisdom about the world, love, friendship, and even The Beatles. His canine observations of human experience provide an avenue into some of the ways blindness might be reconceptualized and "befriended." Uninhibited by the trappings of traditional academic inquiry, Michalko and Goodley are unleashed, free to wander, to wonder, and to provoke within the bonds of trust and respect. Funny and thoughtful, the result is a refreshing exploration and re-evaluation of learned cultural misunderstandings of disabilityBy Jessica Slice. 2024
A much-needed guide to dating—from apps to hooking up, sex, long-term relationships and more—from disabled essayist and author Jessica Slice…
and bioethicist Caroline Cupp. Disabled people date, have casual sex, marry, and parent. Yet our romantic lives are conspicuously absent from the media and cultural conversation. Sexual education does not typically address the specific information needed by disabled students. Mainstream dating apps fail to include disability as an aspect of one's identity alongside race, ethnicity, gender identity, and sexual orientation. The few underutilized disability-focused apps are paternalistic and unappealing. Bestselling dating books do not address disability, and the few relationship books marketed to disabled people focus on the mechanics of sex rather than the complex interactions that create the conditions for it. In Dateable , disabled authors Jessica Slice Caroline Cupp team up to address the serious gap in the dating space. Dateable is the first book on disabled dating and relationships; it's a dating guide made especially for disabled and chronically ill people, that also calls in nondisabled readers. Jessica and Caroline take on everything from rom-com representation and dating apps to sex and breakups with a strong narrative underpinning and down-to-earth advice. The book is as much a practical tool as it is an empowering guideBy Marian Schembari. 2024
One woman's decades-long journey to a diagnosis of autism, and the barriers that keep too many neurodivergent people from knowing…
their true selves Marian Schembari was thirty-four years old when she learned she was autistic. By then, she'd spent decades hiding her tics and shutting down in public, wondering why she couldn't just act like everyone else. Therapists told her she had Tourette's syndrome, obsessive-compulsive disorder, sensory processing disorder, social anxiety, and recurrent depression. They prescribed breathing techniques and gratitude journaling. Nothing helped. It wasn't until years later that she finally learned the truth: she wasn't weird or deficient or moody or sensitive or broken. She was autistic. Today, more people than ever are diagnosed with autism spectrum disorder. Testing improvements have made it easier to identify neurodivergence, especially among women and girls who spent decades dismissed by everyone from parents to doctors, and misled by gender-biased research. A diagnosis can end the cycle of shame and invisibility, but only if it can be found. In this deeply personal and researched memoir, Schembari's journey takes her from the mountains of New Zealand to the tech offices of San Francisco, from her first love to her first child, all with unflinching honesty and good humor. A Little Less Broken breaks down the barriers that leave women in the dark about their own bodies, and reveals what it truly means to embrace our differencesFounder of advocacy organization Diversability and creator of the viral Anti-Ableism Series on TikTok, Tiffany Yu takes readers on a…
revelatory examination of disability—how to unpack your biases and build a disability-inclusive and accessible world. As the Asian American daughter of immigrants, living with PTSD and a permanent arm injury sustained at age nine, Tiffany Yu is well aware of the intersections of identity that affect us all. She navigated the male-dominated world of corporate finance as an investment banker at Goldman Sachs before founding Diversability, an award-winning community business run by disabled people building disability pride, power, and leadership. Organized from the personal to the professional, the domestic to the political, the Me to the We to the Us, The Anti-Ableist Manifesto frames context for conversations, breaks down the language of ableism, identifies microaggressions, and proposes real actions that lead to genuine and authentic allyship. How do we remove ableist language from our daily vocabulary? How do we create inclusive events? What are the advantages of hiring disabled employees, and what market opportunity are we missing out on when we don't consider disabled consumers? With contributions from disability advocates, activists, authors, entrepreneurs, scholars, educators, and executives, Yu celebrates the power of stories and lived experiences to foster the proximity, intimacy, and humanity of disability identities that have far too often been "othered" and rendered invisible. The Anti-Ableist Manifesto is an essential book for going beyond mere awareness and becoming an active anti-ableist working form a more equitable society for allBy Gabrielle Drolet. 2025
A humorous, profound debut memoir about chronic pain, accessibility, and young adulthood, by an acclaimed essayist and cartoonist.In 2021, Gabrielle…
Drolet developed a condition that made her unable to use her hands. It only worsened over time, and as a writer and artist, she had to learn new ways of creating and expressing herself. The experience completely changed her life and her outlook. Look Ma, No Hands explores both the difficulty and the humour of developing chronic and life-altering pain in her twenties. Each chapter looks at a different aspect of her life touched by her disability: how she learned to write when she couldn’t type; how she learned to manage the most mundane daily tasks. She moves cities and as her work as a writer and cartoonist builds has to navigate different byzantine health systems without the privilege or security of having a family doctor, even as she moves into her new apartment and embarks on first dates. And she does all of this with the most wonderful sense of the absurd. Look Ma, No Hands is utterly charming and shares profound reflections on life’s curveballs, and explores how, in Drolet’s words, "you can live a full—even funny—life in a disabled body."By Emily Macrae. 2024
How can we build more accessible cities? Living Disability brings together vibrant perspectives on disability justice and urban systems. A…
musician and snow removal expert, a queer curator, a public pool aficionado, and a journalist turned city councillor - these are just some of the disabled writers exploring disability justice, analyzing urban systems, and proposing more equitable approaches to city building in this anthology. Essays and interviews push the conversation about accessibility beyond policy papers and compliance checklists to show how disabled people are already creating more inclusive spaces in cities of all sizes. Living Disability is universal in scope but intimate and local in focus, grounded in personal struggles and celebrations. Decisions about public transit, affordable housing, and park design all disproportionately impact disabled communities; by sharing stories and strategies, contributors consider the ways disabled thinkers and doers are embracing overlooked aspects of urban design and tackling the toughest problems facing cities. Each chapter provides context to welcome both disabled and non-disabled readers into conversations about the future of inclusion so that all readers can develop their own understanding of what accessible cities look and feel like. This book appeals to city builders of all stripes committed to learning from and working with underrepresented communities. It equips architects, designers, community leaders, innovators, and citizens with the key concepts they need to collaborate with rather than care for disabled neighbors. " Living Disability is at once hopeful and infuriating, solemn and joyous. The stories shared within these pages point to both the past and future simultaneously - illuminating the struggles and joys and history of disabled life, while putting access barriers on blast in a way that is more necessary than ever. The deep, rich work of this collection lies in its embrace of complexity, community, grief, and also its belief in the capacity of our world (read: us) to change. May these stories touch your heart, kindle the flame of your anger, and move you forward into fighting for the better world we all deserve." - Amanda Leduc, author of Disfigured: On Fairy Tales, Disability, and Making SpaceBy Amit Patel. 2020
From the challenges of travelling when blind to becoming a parent for the first time, Kika & Me is the…
moving, heart-warming and inspirational story of Dr Amit Patel 's sight-loss journey and how one guide dog changed his world. 'Inspiring and compelling . . . rekindles one's faith in human nature' - Andrew Marr Amit Patel is working as a trauma doctor when a rare condition causes him to lose his sight within thirty-six hours. Totally dependent on others and terrified of stepping outside with a white cane after he's assaulted, he hits rock bottom. He refuses to leave home on his own for three months. With the support of his wife Seema he slowly adapts to his new situation, but how could life ever be the way it was? Then his guide dog Kika comes along . . . But Kika's stubbornness almost puts her guide dog training in jeopardy – could her quirky personality be a perfect match for someone? Meanwhile Amit has reservations – can he trust a dog with his safety? Paired together in 2015, they start on a journey, learning to trust each other before taking to the streets of London and beyond. The partnership not only gives Amit a renewed lease of life but a new best friend. Then, after a video of an irate commuter rudely asking Amit to step aside on an escalator goes viral, he sets out with Kika by his side to spread a message of positivity and inclusivity, showing that nothing will hold them back. 'An incredible story of courage, perseverance and, ultimately love' - Sun 'The most moving book of the year' - The LadyBy David S Tatel. 2024
A memoir by one of America's most accomplished public servants and legal thinkers—who spent years denying and working around his…
blindness, before finally embracing it as an essential part of his identity. David Tatel has served nearly 30 years on America's second highest court, the United States Court of Appeals for the D.C. Circuit, where many of our most crucial cases are resolved—or teed up for the Supreme Court. He has championed equal justice for his entire adult life; decided landmark environmental and voting cases; and embodied the ideal of what a great judge should be. Yet he has been blind for the past 50 of his 80-plus years. Initially, he depended upon aides to read texts to him, and more recently, a suite of hi-tech solutions has allowed him to listen to reams of documents at high speeds. At first, he tried to hide his deteriorating vision, and for years, he denied that it had any impact on his career. Only recently, partly thanks to his first-ever guide dog, Vixen, has he come to fully accept his blindness and the role it's played in his personal and professional lives. His story of fighting for justice over many decades, with and without eyesight, is an inspiration to us allThis program is read by the authors and a full cast. YouTube sensations Shane and Hannah Burcaw are back with…
a groundbreaking, uproarious collection of essays and short stories about what it means to be in an interabled relationship. With their signature wit and hilarious voice, authors, bloggers, and entrepreneurs Shane and Hannah Burcaw share a true story collection of sweet and unforgettable love stories about interabled couples. Follow the lives of several couples as they navigate their love story in an ableist world. Sometimes tear-jerking, sometimes funny, and always heartwarming, this moving collection comprised of interviews and short stories - with interludes from Shane and Hannah about their own dating and marriage journey - will have readers laughing and sobbing as they discover true stories of love and commitmentWise, visceral essays on navigating pain, sex, trauma, spirituality, addiction, recovery, and grief from queer, neurodivergent trauma-resolution guide Jessica Graham…
In an unapologetic look at living well with trauma and chronic illness, writer and meditation teacher Jessica Graham offers smart, funny, raw, and mindful insights on untangling—and embracing—the messy realities of being a human alive on this planet today. Graham gives us permission to accept care—and accept that it’s okay to want care. They weave together personal stories and practical wisdom, offering their take on managing symptoms, getting creative, setting boundaries, and healing from ableist tropes like “you don’t look sick” and “we’re all a little ADHD.” Graham also shares vulnerable personal history: The adverse childhood experiences that wired their body and brain. The workaholism and addictions that kept their pain lying just below the surface. How illness and trauma intersect to obscure the knowledge that we’re each enough, wholly as we are. This memoir explores the parts of chronic illness life that don’t get enough airtime: How can we center sex and pleasure when pain gets in the way? How can we live well while living through late-stage capitalist hell? How can we come into relationship with our pain without falling prey to self-blame, magical thinking, or toxic positivity? Wise and embodied, fearless and necessary, Being (Sick) Enough is both a wild awakening and a love letter to your whole self: the pains and suffering, joys and brightness, and vital connections that hold each of us as we navigate what it means to be here, like this, right nowBy Amit Patel. 2020
Amit Patel is working as a trauma doctor when a rare condition causes him to lose his sight within thirty-six…
hours. Totally dependent on others and terrified of stepping outside with a white cane after he's assaulted, he hits rock bottom. He refuses to leave home on his own for three months. With the support of his wife Seema he slowly adapts to his new situation, but how could life ever be the way it was? Then his guide dog Kika comes along.... But Kika’s stubbornness almost puts her guide dog training in jeopardy – could her quirky personality be a perfect match for someone? Meanwhile Amit has reservations – can he trust a dog with his safety? Paired together in 2015, they start on a journey, learning to trust each other before taking to the streets of London and beyond. The partnership not only gives Amit a renewed lease of life but a new best friend. Then, after a video of an irate commuter rudely asking Amit to step aside on an escalator goes viral, he sets out with Kika by his side to spread a message of positivity and inclusivity, showing that nothing will hold them back. From the challenges of travelling when blind to becoming a parent for the first time, Kika & Me is the moving, heart-warming and inspirational story of Amit’s sight-loss journey and how one guide dog changed his world.By David S. Tatel. 2024
The "moving, thoughtful, and inspiring memoir" (Bryan Stevenson, author of Just Mercy) by one of America&’s most accomplished public servants…
and legal thinkers—who spent years denying and working around his blindness, before finally embracing it as an essential part of his identity. David Tatel has served nearly 30 years on America&’s second highest court, the United States Court of Appeals for the D.C. Circuit, where many of our most crucial cases are resolved—or teed up for the Supreme Court. He has championed equal justice for his entire adult life; decided landmark environmental and voting cases; and embodied the ideal of what a great judge should be. Yet he has been blind for the past 50 of his 80-plus years. Initially, he depended upon aides to read texts to him, and more recently, a suite of hi-tech solutions has allowed him to listen to reams of documents at high speeds. At first, he tried to hide his deteriorating vision, and for years, he denied that it had any impact on his career. Only recently, partly thanks to his first-ever guide dog, Vixen, has he come to fully accept his blindness and the role it's played in his personal and professional lives. His story of fighting for justice over many decades, with and without eyesight, is an inspiration to us all.By Edited by Alice Wong. 2024
The much-anticipated follow up to the groundbreaking anthology Disability Visibility: another revolutionary collection of first-person writing on the joys and…
challenges of the modern disability experience, and intimacy in all its myriad forms.What is intimacy? More than sex, more than romantic love, the pieces in this stunning and illuminating new anthology offer broader and more inclusive definitions of what it can mean to be intimate with another person. Explorations of caregiving, community, access, and friendship offer us alternative ways of thinking about the connections we form with others—a vital reimagining in an era when forced physical distance is at times a necessary norm. But don't worry: there's still sex to consider—and the numerous ways sexual liberation intersects with disability justice. Plunge between these pages and you'll also find disabled sexual discovery, disabled love stories, and disabled joy. These twenty-five stunning original pieces—plus other modern classics on the subject, all carefully curated by acclaimed activist Alice Wong—include essays, photo essays, poetry, drama, and erotica: a full spectrum of the dreams, fantasies, and deeply personal realities of a wide range of beautiful bodies and minds. Disability Intimacy will free your thinking, invigorate your spirit, and delight your desires.By Jessica Slice, Caroline Cupp. 2024
A much-needed guide for disabled and chronically ill people to dating - from apps to hooking up, sex, and more…
- from disabled essayist and author Jessica Slice and bioethicist Caroline Cupp. Disabled people date, have casual sex, marry, and parent. Yet our romantic lives are conspicuously absent from the media and cultural conversation. Sexual education does not typically address the specific information needed by disabled students. Mainstream dating apps fail to include disability as an aspect of one&’s identity alongside race, ethnicity, gender identity, and sexual orientation. The few underutilized disability-focused apps are paternalistic and unappealing. Bestselling dating books do not address disability, and the few relationship books marketed to disabled people focus on the mechanics of sex rather than the complex interactions that create the conditions for it. In Dateable, disabled authors Jessica Slice Caroline Cupp team up to address the serious gap in the dating space. Dateable is the first book on disabled dating and relationships; it&’s a dating guide made especially for disabled and chronically ill people, that also calls in nondisabled readers. Jessica and Caroline take on everything from rom-com representation and dating apps to sex and breakups with a strong narrative underpinning and down-to-earth advice. The book is as much a practical tool as it is an empowering guide.Tiffany Yu takes readers on a revelatory examination of disability—how to unpack biases and build an inclusive and accessible world.…
As the Asian American daughter of immigrants, living with PTSD, and sustaining a permanent arm injury at age nine, Tiffany Yu is well aware of the intersections of identity that affect us all. She navigated the male-dominated world of corporate finance as an investment banker at Goldman Sachs before founding Diversability, an award-winning community business run by disabled people building disability pride, power, and leadership, and creating the viral Anti-Ableism series on TikTok. Organized from personal to professional, domestic to political, Me to We to Us, The Anti-Ableist Manifesto frames context for conversations, breaks down the language of ableism, identifies microaggressions, and offers actions that lead to authentic allyship. • How do we remove ableist language from our daily vocabulary? • How do we create inclusive events? • What are the advantages of hiring disabled employees, and what market opportunities are we missing out on when we don&’t consider disabled consumers? With contributions from disability advocates, activists, authors, entrepreneurs, scholars, educators, and executives, Yu celebrates the power of stories and lived experiences to foster the proximity, intimacy, and humanity of disability identities that have far too often been &“othered&” and rendered invisible.By Null Jessica Graham. 2025
Wise, visceral essays on navigating pain, sex, trauma, spirituality, addiction, recovery, and grief from queer, neurodivergent trauma-resolution guide Jessica GrahamIn…
an unapologetic look at living well with trauma and chronic illness, writer and meditation teacher Jessica Graham offers smart, funny, raw, and mindful insights on untangling—and embracing—the messy realities of being a human alive on this planet today.Graham gives us permission to accept care—and accept that it&’s okay to want care. They weave together personal stories and practical wisdom, offering their take on managing symptoms, getting creative, setting boundaries, and healing from ableist tropes like &“you don&’t look sick&” and &“we&’re all a little ADHD.&”Graham also shares vulnerable personal history: The adverse childhood experiences that wired their body and brain. The workaholism and addictions that kept their pain lying just below the surface. How illness and trauma intersect to obscure the knowledge that we&’re each enough, wholly as we are.This memoir explores the parts of chronic illness life that don&’t get enough airtime: How can we center sex and pleasure when pain gets in the way? How can we live well while living through late-stage capitalist hell? How can we come into relationship with our pain without falling prey to self-blame, magical thinking, or toxic positivity?Wise and embodied, fearless and necessary, Being (Sick) Enough is both a wild awakening and a love letter to your whole self: the pains and suffering, joys and brightness, and vital connections that hold each of us as we navigate what it means to be here, like this, right now.By Null Shane Burcaw, Null Hannah Burcaw. 2025
YouTube sensations Shane and Hannah Burcaw are back with a groundbreaking, uproarious collection of essays and short stories about what…
it means to be in an interabled relationship.With their signature wit and hilarious voice, authors, bloggers, and entrepreneurs Shane and Hannah Burcaw have put together a true story collection of sweet and unforgettable love stories about interabled couples.Follow the lives of several couples as they navigate their love story in an ableist world. Sometimes tear-jerking, sometimes funny, and always heartwarming, this moving collection comprised of interviews and short stories - with interludes from Shane and Hannah about their own dating and marriage journey - will have readers laughing and sobbing as they discover true stories of love and commitment.By Gabrielle Drolet. 2025
A humorous, profound debut memoir about chronic pain, accessibility, and young adulthood, by an acclaimed essayist and cartoonist.In 2021, Gabrielle…
Drolet developed a condition that made her unable to use her hands. It only worsened over time, and as a writer and artist, she had to learn new ways of creating and expressing herself. The experience completely changed her life and her outlook. Look Ma, No Hands explores both the difficulty and the humour of developing chronic and life-altering pain in her twenties. Each chapter looks at a different aspect of her life touched by her disability: how she learned to write when she couldn&’t type; how she learned to manage the most mundane daily tasks. She moves cities and as her work as a writer and cartoonist builds has to navigate different byzantine health systems without the privilege or security of having a family doctor, even as she moves into her new apartment and embarks on first dates. And she does all of this with the most wonderful sense of the absurd. Look Ma, No Hands is utterly charming and shares profound reflections on life&’s curveballs, and explores how, in Drolet&’s words, &“you can live a full—even funny—life in a disabled body.&”