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How to Tell When We Will Die expands upon Hedva's paradigm-shifting perspective in a series of slyly subversive and razor-sharp essays that range from the theoretical to the personal―from Deborah Levy and Susan Sontag to wrestling, kink, mysticism, death, and the color yellow.

Vier Jahre lang schien die Welt um mich herum weiterzulaufen, während ich in einer unsichtbaren Blase gefangen war. Von lähmender Angst, tiefer Unsicherheit und sozialer Isolation geprägt, verließ ich kaum das Haus und kämpfte täglich gegen meine innere Stimme, die mich immer wieder zurückzog. Dieses Buch erzählt offen und ehrlich von meiner persönlichen Reise durch die Dunkelheit einer schweren psychischen Erkrankung. Es beschreibt den Schmerz des Alleinseins, die Verzweiflung, die Frage nach der eigenen Stärke – und vor allem den unerschütterlichen Willen zur Veränderung.

Up All Night not only grips listeners in unrelenting humor, but it offers a fresh voice embracing listeners with graphic injuries, tender recollections, big surprises, and love. Posing nuanced psychological questions while never losing its heart, Up All Night traces the challenges of living with undiagnosed Asperger's syndrome before the social disorder became known in 1992.

As a result of complications during the birthing process, Amanda was born with cerebral palsy. This book recounts the trauma she experienced as a child, enduring physical, mental, sexual, and emotional abuse from her family, and having a mother who cannot tolerate her cerebral palsy. Amanda found comfort and solace in her grandmother, her '"Gragwa", throughout her childhood. Amanda exposes the naked truth of life with cerebral palsy as she deals with growing up and various relationship issues, friendship issues, loss, and many other things.

Close your eyes and get ready to see the world in a new and more positive way. As a child in Toronto, Molly Burke was diagnosed with retinitis pigmentosa and became completely sightless as a teenager. Now an award-winning YouTube star and global influencer, Molly shares what it’s like to be a purple-haired, pink-obsessed fashion and makeup lover in a seeing world. She speaks with authenticity and candor about how she tackles the preconceived notions we have around blindness; Molly has made it her mission to make us see her - and ourselves- in a wholly empowering way.

On an island off the coast of Massachusetts, six miles across the cobalt blue Waters of the Nantucket Sound, there is a place where hope flourishes. The island is Martha’s Vineyard. The place is Camp Jabberwocky, a sleepover summer camp for people with a variety of disabilities.

In Pass the Salt, Robert Kingett invites you into his world of online dating in 2010s Chicago–a world filled with unexpected challenges, outrageous encounters, and more than a few colorful characters. As a gay man navigating not only the complexities of love but also life with disabilities, Robert’s journey is anything but ordinary.

Science writer Lorraine Boissoneault has been in pain for most of her adult life. Unable to control or make sense of her chronic illness diagnoses, she began describing the ebb and flow of her symptoms as “body weather.” At first an imaginative approach to coping with flare-ups, the phrase has become a waypoint in Lorraine’s explorations of the intimate relationship between our fragile bodies and the fragile world around us.

On t'a appris que le handicap était une faiblesse. Qu'il limitait les possibles. Qu'il condamnait à une vie en retrait. Et si c'était tout l'inverse ? Virginie Delalande est née dans le silence. On lui a prédit l'échec. Elle a choisi la vie.

Ce parcours c'est avant tout une belle histoire d'amour. Une histoire à deux qui malheureusement se termine mais accroît le désir inconditionnel de devenir père, le combat d'un homme pour connaître la paternité, y compris seul. À travers ce témoignage, Mathieu Ceschin se livre sans filtre sur ce combat, celui d'une vie, pour toucher à la paternité.

We meet Andrew Leland as he’s suspended in the liminal state of the soon-to-be blind: he’s midway through his life with retinitis pigmentosa, a condition that ushers those who live with it from sightedness to blindness over years, even decades. He grew up with full vision, but starting in his teenage years, his sight began to degrade from the outside in. Soon— but without knowing exactly when—he will likely have no vision left. Full of apprehension but also dogged curiosity, Leland embarks on a sweeping exploration of the state of being that awaits him.

The entire world knows Michael J. Fox as Marty McFly, the teenage sidekick of Doc Brown in Back to the Future; as Alex P. Keaton in Family Ties; as Mike Flaherty in Spin City; and through numerous other movie roles and guest appearances on shows such as The Good Wife and Curb Your Enthusiasm. Diagnosed at age 29, Michael is equally engaged in Parkinson’s advocacy work, raising global awareness of the disease and helping find a cure through The Michael J. Fox Foundation for Parkinson's Research, the world's leading nonprofit funder of PD science.

Meine Mutter war Alkoholikerin. Meine Kindheit? Keine einfache! Vor Jahren schwör ich mir, den Kontakt zu meiner Mutter abzubrechen. Als sie jedoch schwer erkrankte und Hilfe brauchte, reichte ich ihr meine Hand. Nichtwissend, dass die härtesten Tage, Wochen und Monate meines Lebens sein sollten.

By entitling his book The God Who Enables, Timothy Burdick proceeds to develop in great detail, chapter-by-chapter, that although physically blind from birth, he has been enabled to "see" so much of what the majority who are sited have chosen not to see. Unlike Timothy, they close their eyes and hearts to what our God has and wants for each of us, to see and understand with both hearts and our minds.

After a catastrophic ski accident left him permanently paralyzed from the waist down, Jason not only had to relearn basic tasks like dressing and bathing but also had to wrestle with the harder questions: why do bad things happen? If God is good and powerful, why does he allow suffering? And how does one cope with suffering, which in one way or another visits us all?

Die Autorin ist Mutter eines Jungen im Autismus-Spektrum. Seit einigen Jahren lebt sie mit ihrer Familie in Deutschland, wo sie jeden Tag das Leben aus einer anderen Perspektive kennenlernt – durch das Prisma der Mutterschaft, der Auswanderung und der einzigartigen Welt ihres Sohnes.

La vita di Carlotta Gilli è stata sconvolta all'età di sei anni, quando la malattia di Stargardt, una retinopatia degenerativa, ha ridotto progressivamente la sua vista, portandola da dieci decimi a un solo decimo.

Get ready to embrace your inner warrior with Kelly-Anne Kerley's real and raw story of resilience and HOPE. Dive into her empowering story, celebrating her strength and transformation—because conquering adversity needs to be showcased with laughter and tears.

When Molly Burke was four years old, she was diagnosed with retinitis pigmentosa, a rare degenerative eye disease that leads to eventual blindness, forcing her to see the world through new eyes—literally. Growing up disabled didn’t stop her from playing sports, becoming a rock-climbing instructor, or winning a beauty pageant, but other people’s narrow perceptions of her held her back. Years of relentless bullying, toxic work environments, a rodent-infested apartment, and life’s lowest moments were juxtaposed with red carpets, first-class flights, and personal and professional achievements.

Most people encounter disability at some point in their lives, either in their own bodies or through a friend or loved one. Faith leaders, sacred texts, and members of religious communities frequently offer religious teachings and metaphors as explanation for the presence of disability, but rarely do we hear the voices of people living with disabilities reflecting on their experiences of God, faith, or religious life.