Disability Biography

Linda Dezenski pulls no punches in this raw and revealing memoir. Born with Cerebral Palsy, Linda takes us on a rollercoaster ride through the ups and downs of life with a body that doesn't always cooperate and a society that often misunderstands. But Getting to the Real Me isn't just about struggles—it's a story of triumph. With humor and heart, Linda shares her lightbulb moment: disability doesn't define her, it's just part of the package. Join Linda as she learns to embrace her whole self and discovers her mission to help others do the same.

Wayne Magee is on a mission to empower those who have been repeatedly told, “You can’t!” He has spent his life overcoming obstacles and negative labels intended to convince him that he could not lead a purposeful, fulfilled life. At birth, he was diagnosed with cleidocranial dysplasia, which is a rare genetic skeletal disorder that affects one in one million people. Countless medical professionals stated that he would not live beyond two years old. Wayne’s story demonstrates that for every tough blow, we have an innate ability to overcome societal and medical challenges.

When fourth grader Alex Schwartz first met his cello, his eyes lit up with wonder, and a smile appeared on his face as bright as the potential his new cello teacher saw within him. The cello positively impacted all aspects of his development, including focus, fine motor, and gross motor skills.

During an ordinary Fall afternoon, Kimber Hanchey-Ogden was delivered devastating news: Seth, her 17-year-old son, had been hit by a car and airlifted to a hospital! Having sustained a traumatic brain injury, doctors told her that if Seth made it, he would never be able to walk or talk; he would not remember his past or understand humor. And that was just for starters.

"La situazione di Cesare è molto grave. È giusto che te lo dica. Fate tutto quello che potete con lui, non rimandate." La storia di Valentina, Federico, Ale, Terry e Cece si è interrotta qui, tra le mura di un ospedale e la paura di non avere più tempo. Loro, però, si erano Fatti una promessa: anche nei momenti più bui, tra le ombre, avrebbero cercato la felicità. Così, tra feste di compleanno e gite in canoa, la loro storia continua, e con l’estate ormai alle porte il loro viaggio diventa molto di più.

Ellen Keane spent most of her teens uncomfortable with her limb difference and battling to hide her insecurities. It was only when she embraced her difference that she found her superpower. She started to believe in her unique abilities and gradually find the success that she had never dreamed possible. Perfectly Imperfect is for anyone struggling to accept who they are. With anecdotes from her own life, practical advice and good-natured humour, Keane challenges you to let go of waiting until everything is perfect and instead embrace your imperfections and accept who you are, flaws and all.

Embark on a powerful and inspirational journey with Dawn Green as she battles against the odds in a 35-year-long quest to uncover the truth behind her mysterious and life-threatening health issues. This gripping memoir takes listeners through the highs and lows of an extraordinary life marked by persistence, resilience, and unwavering hope. The book opens with the author's early years, when she first realized that her health was beginning to decline. In succession, a series of perplexing symptoms began to plague her.

AUTISM UNLEASHED, GENIUS UNLEASHED celebrates the lives and achievements of 13 autistic visionaries, illuminating the profound contributions they have made in a variety of fields. These stories are not only a testament to their genius but also a beacon of hope and inspiration for anyone touched by autism.

When her son was diagnosed with autism at the age of three, Irma Velasquez was devastated. It was the pre-internet era of the early 1990s, and both information and experts were hard to find. Desperate for answers, she sought out therapists and educational programs designed to teach Aaron how to become successful in school and in life. But those early years ended up teaching Irma more than they taught Aaron. Irma realized her desire to "fix" her son had been a masquerade to fulfill her own needs, and she began to love him just as he was: perfect.

In less than sixty days, published author and family chiropractor Kristi Hellenbrand would suddenly lose the ability to walk. The brightest doctors would not be able to figure out why. Part memoir, part research thesis, the author reveals with raw honesty her journey through Lyme Disease and the seemingly impossible passage to rediscovering wellness. In 2020, a sudden and mysterious illness - said to not exist in Georgia - took everything from her. This is the story of the deep, dark place where only grief takes you, but also the story of how she saves her own life.

In 2012, combat engineer Curtis McGrath was serving in the Australian army in Afghanistan when, in the line of duty, he stepped on a mine. Seriously injured but still conscious and aware he'd bleed out and die within minutes, McGrath, as the unit's chief first-aid officer, directed his comrades to apply tourniquets and administer an IV and morphine. Then, as he was stretchered to a helicopter, fearing he would never see his family again, he joked that he planned to become a Paralympian.

Weaving together memoir, criticism, and cultural history, and touching on both the spectrum of the deaf experience and how society fails deaf people, Antrobus finds his own way to reclaim his deafness as a power and a joy, and to reconcile his relationship to words and the world around him.

L'inizio di questa storia è un incrocio nel bel mezzo di Tripoli, più che un incrocio, un'auto con un parabrezza rotto ferma a un incrocio dopo un incidente. A bordo della macchina un uomo e una donna, un padre e una madre, prima erano in tre, solo che la figlia poco più che neonata è stata sbalzata fuori dall'abitacolo e ha impattato contro un albero. Comincia così il racconto della vita di Nagla Augelli, bambina tunisina abbandonata dalla famiglia in un orfanotrofio della sua città, dopo che un incidente di auto l'ha resa paraplegica.

Told through an experimental mix of intimate anecdotes and interactive visuals, this book immerses listeners in Emmy Award–winning documentary filmmaker James Robinson's point of view, allowing them to see the world through his disabling eye conditions.

Der Wunsch, den Jakobsweg zu wandern und einfach mal rauszukommen, ist für viele Menschen ein Traum - egal, ob man gesund, stark und ausdauernd ist. Auch Menschen mit Behinderung gehen diesen Weg, um ihre Grenzen auszutesten, um auf ein Wunder zu hoffen oder vielleicht, um mal etwas anderes zu erleben. Genau das will ich auch. Etwas Neues sehen und hören - auch als Nichtsehender und Nichthörender, denn ich bin taubblind. Ich möchte dich auf meine Reise mitnehmen. Hier in meinem Buch kannst du mich begleiten.

In God’s Got Jokes, author Neosho C. Ponder, allows the listener into the most personal and vulnerable parts of her life. As she battled the hardships of cancer, she learned that some of those who supported her succumbed to their own battles of cancer. You will hear stories such as: Being evicted during chemotherapy, which finally led to her seeing the humor and not choosing to give up. The financial adversity that affects cancer patients too sick to work, those undergoing treatments, and multiple surgeries.

Theirs was an unlikely life together. Sheila gave birth to Josephine on 11th May 1993 and for twenty-three years they co-existed in a loving mother-daughter relationship, but one with a difference. Josephine suffered catastrophic brain injury at birth, never spoke to Sheila, rarely smiled and was barely able to see the faces of the people who loved her.

The Umbrella Picker tells the true story of a woman who was lost for 45 years until she learned that she is Autistic. After a long and relentless journey of searching for answers, the hand of fate finally revealed to her what she had waited a lifetime for. Learning she was Autistic was life changing. She is no longer lost, and having found her own, unique way, Jane has written the (brutally honest!) book she wished was available to her years earlier.

Her Name Was Lola is the story of Trish Ryan’s triumphant recovery from a stroke that should have killed her. She had a successful career in the entertainment industry for over 30 years until May 5th, 2017, when she suffered a severe stroke that changed her life forever. Living a very fast-paced life had not prepared her for when it all came to a grinding halt. Lost and confused with no roadmap to follow, she relied on her faith to show her the way to embrace what happened and move forward.

This book is about one big rollercoaster. It's about a girl who has CP (cerebral palsy) and the challenges she has faced throughout her life. A girl who is lucky to be blessed with people who stood beside her all the way. A girl who tries to do it all and doesn't let her CP get in the way of life. She just goes with it!