Showing results by publisher "-emdashery books-" in People with Disabilities

Hey guys, you might know me already from one of my social media channels where I talk about the highs and lows of living with Tourette's syndrome. I've loved sharing those times with you and - as there are lots of things I can't fit into a 60-second video - I've decided to write a book! It's the full story of how I came to be diagnosed and how having Tourette's has changed my life. Writing it has given me an opportunity to talk about things I haven't felt ready to share before - for some reason it's easier to put down private things in written words than in a video!

As autistic children grow into teenagers, you will experience new challenges, both as a parent and as a family. Supporting the leap into adulthood can seem daunting, but here Carrie Cariello takes you through her journey with her son Jack, shining a light on how to help your young person prepare for different life stages and grow in independence. Carrie's own experiences form the basis of her deeply empathetic advice—in this warm, astute and thoughtful book she offers a guiding and steadying hand so you can move through periods of change with increased confidence and calm.

Half a world away from home in 1976, 18-year old Anne B. Thomas awakens on the side of a two-lane road paralyzed from the chest down. Fast forward through a rigorous year of physical therapy to when her doctor gives her an ominous warning: “You will live a long time and be a burden on your family for the rest of your life unless you check yourself into a nursing home”.

On July 4th, 2013, Connor Sparrowhawk, also known as Laughing Boy or LB, was found dead in a specialist NHS unit. Connor, who had autism and epilepsy, had a seizure while in the bath, and no member of staff was on hand to stop him from drowning. An entirely preventable death. Sara Ryan presents a frank, sometimes funny and touching account of her son's early life and preventable death and the unfolding #JusticeforLB campaign.

"Rediscovering the World: A Journey through Anosmia" explores the little-known condition of anosmia—the loss of the sense of smell. James Rondepierre takes listeners on an inspiring journey, weaving together personal stories and scientific insights to uncover the profound impact of this condition. Through heartfelt narratives, listeners will witness the challenges and triumphs of individuals living with anosmia, from the emotional adjustments to their resilience and creativity in redefining life without smell.

You'll relate, you'll cry, and you'll want to learn more. A story of triumph over tragedy, again. In this moving tale, you'll follow Cristi Bundukamara's life as a blissful newlywed who hopes to give back to the world. Her family grows quickly in the form of both biological and adopted children. Cristi has all that she hoped for and more when a senseless drowning rocks her family. While struggling to pick up the pieces, more tragedy ensues and Cristi has to dig deep to keep moving forward.

It only takes a second to change your life. At age 21, Ryan Atkins had everything going for him: A full-ride scholarship in a prestigious business program, a well-paying internship, an opportunity to pitch a business plan to venture capitalists in New York City. He was living his dreams and preparing for a future of success. But the day before leaving for New York, Ryan was in a life-altering car accident that robbed him of the use of his arms and legs. Paralyzed from the shoulders down, he found himself struggling to grasp just how fundamentally his life had changed.

Ben Mattlin lives a normal, independent life. Why is that interesting? Because Mattlin was born with spinal muscular atrophy, a congenital weakness from which he was expected to die in childhood. Not only did Mattlin live through childhood, he became one of the first students in a wheelchair to attend Harvard, from which he graduated and became a professional writer. His advantage?

I finished my first book, Multiple Sclerosis: A Blessing in Disguise, around the end of 1998. At that time, I was going through a lot of issues that I thought were very important to me. That book told of my discovery, my eventual acceptance of the illness, and how I dealt with what was happening to me. Like anybody else who is faced with the burden of discovery, I had a lot of questions that I felt I really needed to answer, but I never sought to answer why this had happened to me.

Nathan Glad was not expected to survive birth. Born with OI (Osteogenesis Imperfecta), also known as Brittle Bone, he has faced remarkable life challenges. Despite it all, Nathan remains determinately happy. This book contains his 7 Hacks for Happiness.

In 2011, three years after leaving the NFL, Steve Gleason was diagnosed with ALS, a terminal disease that paralyzes the entire body. Doctors gave him three years to live. He was thirty-four years old. As Steve says, he is now ten years past his expiration date. His memoir is the chronicle of a remarkable life, one filled with optimism and joy, despite the trauma and pain and despair he has experienced.

This book explores the untold story of a war veteran's journey with transcranial magnetic stimulation treatment.

This English professor grew up spacey and overweight. Drowning in the unrealistic demands of motherhood, Livingston steals her son's ADHD medication and watches it transform her life—for good and bad. She grows weary of subjective diagnoses and chemical treatments from traditional psychology experts, and experiments with functional medicine—brain mapping and nutritional supplements—as a way to understand her brain's potential, bio-hacking her way to a healthy body and mind.

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.

Raymond Antrobus was first diagnosed as deaf at the age of six. He discovered he had missing sounds—bird calls, whistles, kettles, alarms. Teachers thought he was slow and disruptive, some didn't believe he was deaf at all. The Quiet Ear tells the story of Raymond's upbringing at the intersection of race and disability. Growing up in East London to an English mother and Jamaican father, educated in both mainstream and deaf schooling systems, Raymond explores the shame of miscommunication, the joy of finding community and shines a light on the decline of deaf education in Britain.

An inspiring and unforgettable memoir that provides hope to others who are experiencing depression, mania, or psychosis, RESILIENT is a deeply personal account about life with mental illness, hearing loss and resiliency. Liz's journey provides encouragement for patients, families, friends, and healthcare workers by showing that recovery is possible.

Our aim with this narrative is to share our journey through the labyrinth of cancer treatment—the decisions we faced, the paths we chose, and, most importantly, the lessons we learned. We hope to offer guidance, support, and perhaps a sense of solidarity to others who find themselves on a similar journey. This is not your typical medical guide; it is a well-researched companion for every aspect of your cancer journey and a deeply personal account of battling cancer from the perspective of a spouse.

Tom Nash has spent his adult life mesmerising audiences around the world, either with his thought-provoking philosophies or hypnotic DJ sets. However, before his career had even begun, Tom was given the slimmest chance of survival after contracting a deadly disease at the age of nineteen, resulting in him losing both his arms and legs. When the unthinkable becomes your reality, where do you turn? Why do you turn? Tom not only went on to survive, but to thrive, taking on life with nothing more than a pair of prosthetic hooks and a dark sense of humour.

With evocative storytelling and incisive research, Katie Rose Guest Pryal brings a new eye to the mental health crisis that higher education has faced for decades. Written from the perspective of a bipolar-autistic professor, A Light in the Tower is both a bracing account of the mental health crisis in higher education and a passionate and informed proposal for how to teach with mental health in mind. Pryal contends that higher education's mental health crisis is the result of long-term systemic problems in education that demand nothing short of a revolution.