Disability Memoir

Ruth's tribe are her lively children and her filmmaker husband, Simon, who has motor neurone disease and can communicate only with his eyes. Ruth's other tribe are the friends who gather at the cove in Greystones, Co. Wicklow, and regularly throw themselves into the freezing cold water just for kicks. The Tragic Wives' Swimming Club, as they jokingly call themselves, meet to cope with the extreme challenges life puts in their way, not to mention the monster waves rolling over the horizon.

In this deeply moving memoir, L.A. Batista recounts her incredible journey through a life filled with obstacles — family turmoil, physical challenges, an abusive marriage, and single parenthood. Despite the hardships, her story is one of unyielding strength and resilience. Beginning with her childhood in the 1960s in a neighborhood in New York City, the author recounts her family life as she dealt with an undiagnosed rare disease.

In 1959, at the age of 21, Max Starkloff was in a car accident that left him paralyzed from the neck down. His doctors doubted he would live longer than a few days, and, if he survived, the hope for his quality of life would be minimal. How did this young man with barely a high school education become the leader of a powerful disability rights movement and the founder of the Starkloff Disability Institute? This is his remarkable story.

This is a very real and bloody look at the journey I made from 19 to 29. I will walk you through the icy halls of drug addiction and dealing, college in Santa Barbara (specifically Isla Vista), depression, suicide, and overdoses. The second part of the book I could only write just recently, as I was, by the Grace of God, able to live the life I knew I always should. Please come with me through the very real and honest look at what it was like to be a young man in the 2010s and how through a million close calls, I finally found life.

This book chronicles the journey of Eritrean-born Joseph Woldu. As a child refugee, he found himself having to adapt to changes of place, language, and customs; then as a man forced to relearn much of the same after involvement in a disastrous accident two days before the 9/11 terrorist attacks. What makes Joseph's story so incredible is not that he survived change and tragedy, but how he continually found the strength to improve himself and his circumstances. His story reflects the importance good relationships play in our lives.

Fred Rutman was certainly up against it. It being the Grim Reaper. The Reaper unleashed its full arsenal, pitting Fred against much of the medical system he trusted with his life. Even if Fred won the initial battles, could he win the war? The Summer I Died Twenty Times is a medical trauma memoir unlike any other. In one package, Fred Rutman provides all the overcoming adversity, resilience and beating the odds a listener expects. With a side of sarcasm and humor. He may not be the hero you expected. He just might be the hero you need.

I Sverige finns mer än en miljon anhöriga som vårdar eller stöttar en närstående med fysisk eller psykisk ohälsa eller funktionsnedsättning. Även om var och en har sin unika historia är det mycket som förenar oss. Anhörig i ett hav av känslor ger röst åt våra berättelser. Om ovisshet och oro, otillräcklighet och frustration, skuld och skam, sorg och maktlöshet. En situation som kan utveckla oss som människor, men också utmana och slita ut oss. Det handlar om avgrunder och guppande känslohav, men också om stillsamma solgläntor och fascinerande utsiktsplatser.

At the age of sixty, and having lived with Parkinson’s disease for over ten years, Guy Deacon CBE set out on one last adventure: to drive solo from his home in the UK 18,000 miles and through twenty-five countries to Cape Town on the southern tip of Africa. This incredible journey, across Europe and down the full length of Africa, took the former British Army officer over twelve months. Along the way, he broke down five times, underwent one emergency evacuation, and took 3,650 prescription pills.

Beyond the nerve is a raw and unfiltered journey through five years of living with pudenda neuralgia—a condition that tested every ounce of my resilience while reshaping my purpose. It delves into the struggles and triumphs of managing chronic pain, the emotional toll of invisible battles, and the lessons learned in advocating for myself when support wasn't always easy to find.

En este libro de memorias profundamente conmovedor y sincero, Blanca Reyes Méndez comparte su viaje tras la pérdida repentina e irreversible de la visión de su ojo izquierdo. A través de la reflexión poética y la verdad personal, explora el dolor, el miedo, la curación y la transformación. Ver con el alma no trata sólo de la pérdida de visión, sino de aprender a ver de otra manera. A encontrar la luz interior. A vivir más despacio, más plenamente y con el corazón bien abierto.

Lorsqu'on rencontre Martin pour la première fois, ce qui frappe immédiatement, c'est son sourire charmeur, son enthousiasme, son oeil qui pétille, son aisance à l'oral et ses idées qui fusent dans tous les sens. Son fauteuil, on n'y pense même pas. On ne le voit pas. C'est tout juste si l'on remarque que ses doigts, qui paraissent pourtant si agiles, sont inertes, tant Martin a de choses à partager, d'anecdotes à raconter et de montagnes à déplacer. Pourtant, Martin est tétraplégique.

Meet the exhausted group of caregiving mothers who offer extraordinary care to a child with disabilities or unique needs. These unsung heroes, who walk invisibly among us, dedicate time, energy, love, and their entire lives to help their loved one who is unable to help themselves. A child with a rare degenerative disease. A sibling with autism. A teen wading through anxiety and depression. An adult child with a debilitating illness. A child with extreme ADHD.

" Bizarrement, en tant que société, nous accordons à la cécité un caractère bien plus dramatique que cette condition physique ne le mérite peut-être. Nous...

Twitch is a frank and funny memoir about picking up the pieces when personal tragedy hits. In 2021, Irish Examiner columnist, stylist, author and podcaster Annmarie O'Connor was diagnosed with early-onset Parkinson's disease, an incurable neurodegenerative condition broadly affecting movement and mental health. Though she is no longer working as a stylist as part of her career due to Parkinson's complications, Twitch outlines her journey from a life-altering diagnosis to becoming an activist and agent of change.

Kathleen O’Neill courageously chronicles her journey through the turbulent realms of bipolar disorder, addiction, and recovery. With raw honesty and resilience, Kathleen shares the battles she fought within herself and against social stigmas, laying bare her struggles, triumphs, and the moments of grace that shaped her healing. This memoir offers a compelling look at the complex layers of mental health , the strength of the human spirit, and the transformative power of hope.

Darlene was a small-town single mother from Arkansas. Bert was a small-town preacher’s son from Oklahoma. Polio crippled both of them as teenagers. When their paths crossed at a rehab center in 1952, these young adults questioned how anything good could come from this crippling virus. Bert’s faith in the Biblical passage of Romans 8:28 gave him hope that “Polio was not good, but God would bring good out of it.” Darlene’s journey to the rehab center was “the one way for God to get me in the right place at the right time.”

While preparing to deploy with the US Army, Marcus suffered a severe spinal injury that left him paralyzed. After dying on the operating table twice, the surgeons saved his life, but told him he'd never walk again. Having no other option, Marcus started doing some brutally honest soul-searching, looking for the lesson to be learned from his injury. Once he started seeing his adversity as a gift instead of a curse, something miraculous began to happen....

This program is read by the author. An inspiring memoir of a young man who discovered he was going completely deaf just at the moment he’d fallen in love for the first time. As a child, Matt Hay didn’t know his hearing wasn’t the way everyone else processed sound—because of the...

Can four words change a life? On a rainy autumn day, four words changed the life of a young cardiology nurse. Four little words hurled across a dimly lit exam room struck fear in a mother’s heart. “You are legally blind.” Anita’s journey through blindness began with the devastating diagnosis of retinitis pigmentosa, an untreatable, degenerative retinal disease. At the age of 33, she was forced to face not only vision loss, but also the loss of driving, her nursing career, and even her independence. Anita was convinced that life was over.

When you hear the word “disability”, what comes to mind? Cheryl Schiltz tells her story of being introduced to disability. She shares her journey from a silent world to one that encased her in constant anxiety. Her life as she knew it had disappeared. It became one of a continuous fight between psychological and physical change. Noise. From her childhood, you’ll find yourself traveling with her as she discovers the power to gain control. She shares her story openly and honestly, raw and sensitive.