Memoirs Special Needs

A sacred journey through grief, healing, and rediscovering life after loss. For 25 years, John and Carla Miller dedicated their lives to loving and caring for their son, Peter Flint Miller—a special needs child who could not walk, talk, or eat without assistance, but whose life overflowed with joy, laughter, and purpose. Every four hours, around the clock, they fed him, changed him, bathed him, dressed him, and prayed over him. And then, one day, it all stopped. Room to Breathe, Room to Grieve is their honest, faith-filled story of what happens after the caregiving ends—after the ...

The world Annette Hines knew exploded when her infant daughter Elizabeth was diagnosed with mitochondrial disease—a degenerative, life-limiting illness. Annette’s joy quickly turned to apprehension and she knew nothing would ever be the same again. Butterflies and Second Chances is the inspiring true story of a mother’s special needs journey, and her struggle to secure the best possible life for her child in the face of bureaucratic resistance and marital crisis. It is a story of sacrifice, dedication, and the life-altering adjustments a special needs parent has to make when ...

What do you do when you wake up in your mid-40s and realize you've been living a lie your whole life? Do you tell? Or do you keep it to yourself? Laura James found out that she was autistic as an adult, after she had forged a career for herself, married twice and raised four children. Odd Girl Out tracks the year of Laura's life after she receives a definitive diagnosis from her doctor, as she learns that 'different' doesn't need to mean 'less' and how there is a place for all of us, and it's never too late to find it.

After three long years, Johnny’s young son, Sam, experiences a breakthrough. But even as calm comes to Sam's body, the illness makes off with his mind. Violent outbursts, strange obsessions - what has happened to his sweet boy? Cinematically weaving three generations of fatherhood, Remember, You’re the Greatest is a memoir of hard questions. Of unexpected joy in the ache of mystery. And the power of a special needs child to teach a father what greatness truly looks like.

Andreas Souvaliotis was raised at a time when being on the autism spectrum wasn't easily diagnosed or even discussed. Minds like his were simply considered odd. He also knew from an early age he was gay, and it terrified him as he was growing up with openly homophobic parents in one of Europe's least tolerant societies. Andreas' differences made him an outsider, right through to his mid-40s. And then suddenly, everything changed. Misfit is the extraordinary memoir of a man who realized there was strength in his strangeness, that it could be used as a force for good.

Owen-known to his family as "little buddy" or "Little B"-has a rare genetic disorder that leaves him largely confined to a wheelchair. Before being united with Haatchi, Little B was anxious and found it difficult to make friends. Haatchi-an adorable Anatolian Shepherd puppy-was abused and left for dead on railroad tracks. He was struck by an oncoming train, and although his life was saved, his leg and tail were partially severed. Haatchi was left massively disabled and totally dispirited.

Caro Giles lives on the far edge of the country, with her tribe of daughters: The Mermaid, The Whirlwind, The Caulbearer and The Littlest One. She is at once alone and yet surrounded. Bound by circumstance, financial constraints, illness and the challenges of single motherhood, she has nowhere to go but the fierce landscape that surrounds her. Over the course of the year, the moon becomes her fellow traveller through dark times, and companion through joyful ones – and even when the sky is wreathed in cloud, the moon is still felt in the pull of the tides.

A late bloomer’s coming-of-age memoir asks how does one accept and free themselves from visible and invisible disabilities and still retain their sense of connection and humor? Nothing Special is a disarmingly candid tale of two sisters growing up in the 1970s in rural Connecticut. Older sister Chris, who has Down syndrome, is an extrovert, while the author, her younger, typically developing sister, shoulders the burdens and grief of her parents.

Kenna was born January 9, 2012, weighing in at a meager 9.6 ounces. She was born 16 weeks too soon. After spending 183 days riding the roller coaster in Club NICU, she is finally home. This is our story of hope, finding happiness in unlikely places, and making the best of the life we have.

When Carla Ciccone is diagnosed with ADHD at thirty-nine—an evaluation prompted by the demands of early motherhood—it flips the script on her life. After years of self-blame and self-sabotage, she discovers that her most reviled traits aren’t deep personality flaws, but symptoms of an undiagnosed disorder. And as she goes from being her own biggest hater to someone a bit more compassionate, she notices the growing community of women in the same situation.

When Allen Shawn and his twin sister, Mary, were two years old, Mary began exhibiting signs of what would be diagnosed years later as autism. Understanding Mary and making her life a happy one appeared to be impossible for the Shawns. With almost no warning, her parents sent Mary to a residential treatment center when she was eight years old. She never lived at home again.

This book is about one mom's journey in raising a child with special needs. Her daughter Lydia has Down syndrome. This is the story of their life together. Kerry Lynn Patton shares the blessings, trials, and what their family has learned by having Lydia in their lives. This is not meant to be a “How To” book for raising a child with special needs, but rather a book to encourage moms, dads, family, and friends. This delightful book is written in whimsical and heartfelt “snippets" for the listener to enjoy a little at a time or easily in one sitting.

Happiness begins with a charming courtship between hopelessly attracted opposites: Heather, a world-roaming California girl, and Brian, an intellectual, homebody writer, kind and slyly funny but loath to leave his Upper West Side studio. Their magical interlude ends, full stop, when Heather becomes pregnant - Brian is sure he loves her, only he doesn't want kids.

Strange Son is the dramatic story (part memoir, part groundbreaking science) of how the author learned to communicate with her severely autistic son through meeting Soma Mukhopadhyay, a poor, single mother from Bangalore, India, whose own son, Tito, is a genius who is also severely autistic.

Patti M. Hall’s life is pitched into an abyss of uncertainty when a golf ball-sized tumour is discovered in her teenage son’s head and he is diagnosed with gigantism, a disease of both legend and stigma. After scrambling to access a handful of medical experts in the field, Patti learns that her son could grow uncontrollably, his mobility could be permanently limited, and his life could be cut short without timely and aggressive treatment. Patti’s attention shifts fully to her son, away from her relationships as well as her own career and health.

At the peak of the Cold War, Mitchell Minor was born to a military family living on Wurtsmith Air Force Base, Michigan. Unknown to his parents, the base's groundwater was contaminated from firefighter foams (PFAS/PFOA), de-greaser, and jet fuel. His mom drank the poisonous water which caused Mitchell’s small head (microcephaly) and other birth defects. This book is for every family who feels overwhelmed and for friends and family to better understand how to help. The Minor family invites you to experience God’s love during their 30-year journey with Mitchell.

Graham Hale Gardner died before turning 23 and never learned to walk or speak due to severe cerebral palsy complicated by epilepsy. Yet he left a legacy of love and compassion that deeply moved scores of people from widely different backgrounds. Graham’s story, written through the eyes of his father, speaks of the enormous legacy left by a boy who never spoke. A story that raises provocative questions about the “invisible lines of connection” that make us human.

I wrote this book because I wanted the world to know the story of my special needs son Lloyd C. Darby lll. Affectionately known as DJ, which stands for Darby Junior. When people triumph over their circumstances as my wife and I have, there are usually hidden lessons others can benefit from contained within the events. However, if we don’t share our stories with the world, no one will ever hear about them.

The remarkable story of how a mother moved from rage to hope after learning her youngest child was dying and harnessed her grief to transform the lives of others. Harnessing Grief will hearten listeners through Maria Kefalas' journey of understanding how to find hope and purpose amongst the most tragic of circumstances.

There are 1.3 billion people around the world who identify as having a disability. When you include friends and family, the disability market touches 53 percent of all consumers. It is the world’s largest emerging market. Unleash Different reveals how companies like Google, PepsiCo, and Nordstrom are attracting people with disabilities as customers and as employees. Replacing “nice to do” with “return on investment” allows market forces to take over and the world’s leading brands to do what they do best: serve a market segment - in this case, the disability market.