Memoirs Special Needs

All Janine Urbaniak Reid ever wanted was for everyone she loved to be okay so she might relax and maybe be happy. Her life strategy was simple: do everything right. This included trying to be the perfect mother to her three kids so they would never experience the kind of pain she pretended not to feel growing up. What she didn’t expect was the chaos of an out-of-control life that begins when her young son’s hand begins to shake.

Margaret Mohrmann has devoted most of her professional life to caring for children, and in Attending Children she shares the remarkable education those children and their families have given her. Her narratives are both painful and hopeful, tragic and funny, full of remarkable characters and sometimes bizarre families.

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.

For Magda Newman, normal was a goal—she wanted her son Nathaniel to be able to play on the playground, swim at the beach, enjoy the moments of childhood that are often taken for granted. But Nathaniel's severe Treacher Collins syndrome—a craniofacial condition—meant that other concerns came first. Could he eat without the aid of a gastrointestinal tube? Could he hear? Would he ever be able to breathe effortlessly?

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.

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.

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.

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.

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.

This is my story. After a lifetime of trying to help everyone else get their lives together, I have finally figured out how to get mine together. I am now 72 years old, semi-retired from a business I created to help young adults with autism function in the world. I live in Mexico with my loving partner. I have fulfilling relationships with my adult children and grandchildren.

When Kate Swenson’s son Cooper was diagnosed with severe, nonverbal autism, her world stopped. She had always dreamed of having the perfect family life — watching her boy play at baseball games, walking him down the aisle. She hadn’t signed up for life as a mother raising a child with a disability.

In November of 1970, the Finell family's lives were changed forever by a family vacation to Acapulco. Seven-year-old Stephanie fell ill soon after their return to the United States, but her mother, Karin, thinking it was an intestinal disorder, kept her home from school for a few days. She was completely unprepared when Stephanie went into violent convulsions on a Friday morning. Following a series of tests at the hospital, doctors concluded she had contracted viral equine encephalitis while in Mexico.

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.

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.

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.

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.

Susan Casserfelts kriminalromaner i Höga kusten-serien har lovprisats och blivit riktiga ljudbokssuccéer. Men medan hennes författarkarriär tog fart brottades hon med svårigheter på det privata planet. När sonen Hugo föddes förstod Susan ganska snart att han var annorlunda, men det dröjde mer än fem år och många läkarbesök innan han slutligen fick sin diagnos: autism. Med hjälp av bildstöd och teckenspråk försöker föräldrarna hantera Hugos många utmaningar. Samtidigt kämpar Susan med att få hjälp för sin egen utmattning.

Follow a mother's journey through the twists and turns of autism spectrum disorder. Planet A is a book that gives the reader a glimpse into the behaviors of a child, Jackie Christiansen, on the autism spectrum. It is real and raw dealing with issues of explosive anger, social ineptness and low maturity, all of which can cause complete confusion and low self-esteem. Parenting can be extremely exhausting and getting the outside world to understand can be challenging. Through IEPs (Individual Education Plans) within the school systems to navigating the causes of behaviors the book is laced ...