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In Pass the Salt, Robert Kingett invites you into his world of online dating in 2010s Chicago–a world filled with unexpected challenges, outrageous encounters, and more than a few colorful characters. As a gay man navigating not only the complexities of love but also life with disabilities, Robert’s journey is anything but ordinary.

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.

Twenty-three-year-old Ardra Shephard is sleeping with the wrong guy, living in a crappy apartment, and spending money she doesn't have on designer shoes, boozy brunches, and weekends in NYC. Making mistakes while you figure stuff out is what your twenties are all about. Then a doctor tells Ardra she has MS, and those two letters split her life into a Before and After.

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.

After a catastrophic ski accident left him permanently paralyzed from the waist down, Jason not only had to relearn basic tasks like dressing and bathing but also had to wrestle with the harder questions: why do bad things happen? If God is good and powerful, why does he allow suffering? And how does one cope with suffering, which in one way or another visits us all?

Die Autorin ist Mutter eines Jungen im Autismus-Spektrum. Seit einigen Jahren lebt sie mit ihrer Familie in Deutschland, wo sie jeden Tag das Leben aus einer anderen Perspektive kennenlernt – durch das Prisma der Mutterschaft, der Auswanderung und der einzigartigen Welt ihres Sohnes.

La vita di Carlotta Gilli è stata sconvolta all'età di sei anni, quando la malattia di Stargardt, una retinopatia degenerativa, ha ridotto progressivamente la sua vista, portandola da dieci decimi a un solo decimo.

Get ready to embrace your inner warrior with Kelly-Anne Kerley's real and raw story of resilience and HOPE. Dive into her empowering story, celebrating her strength and transformation—because conquering adversity needs to be showcased with laughter and tears.

Liz Casper is a former medical doctor, artist, and author from the Pacific Northwest. In her first book, BRILLIANT, BEAUTIFUL, BIPOLAR, Liz shares with us her personal journey before, during, and after her diagnosis of bipolar disorder. The book, set in Los Angeles and Las Vegas, chronicles Liz’s experience both living with and healing from this devastating diagnosis.

After being diagnosed with muscular dystrophy, Melissa Haugen felt alone. In an effort to make others feel seen, she vulnerably shares her personal story of living with muscular dystrophy.

Dietetics practitioners are food and nutrition experts who help people live healthier lives. They work in a variety of settings—from hospitals and research to sports, schools, nursing homes, and the food industry. Yet, despite the diversity of the populations they serve, the dietetics profession is predominantly female, white, and able-bodied. Only 2% of dietetics practitioners have a disability compared to 29% of US adults. There is an urgent need to diversify the field—especially by including practitioners with disabilities.

As a new mother to three nonverbal, profoundly autistic children, Christine Slack Roach felt lost and alone. There were resources about autism and about raising children with disabilities. But she couldn’t find anything that resonated with what she was experiencing with her own children. As her three children approach adulthood, Christine feels compelled to share the miracles, joys, pain and unending love she has experienced learning about and raising her kids so that other parents in a similar situation will know that they are not alone, and there are resources out there.

What do you do when multiple sclerosis knocks you on your ass, tells you your rap career is over, and dares you to stay down? You write a new story — and this one’s real as hell. Myelin My Shoes is the raw, unfiltered, punch-in-the-gut memoir from underground hip-hop artist Robert “B-Cide” Cardillo II, who turned pain into power and built something real in a world full of fake. From rocking shows with legends to dodging shady promoters, from touring the country to being forced into a wheelchair by multiple sclerosis — this is the story of a man who refused to tap out. No ghostwriters.

What it really feels like to live with type 1 diabetes—true stories inside. If you’ve ever felt overwhelmed, frustrated, or alone with type 1 diabetes, this book is for you. Written by Neil Greathouse (@thebetes), Type 1 Diabetes – True Stories is a powerful collection of honest, hilarious, and sometimes heartbreaking moments from over 30 years of living with T1D.

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.

We are all born with a series of gifts and curses. It is my experience, that some of those form your self-identity, and dictate much of your life. Attention Deficit Disorder was mine. Growing up I felt hindered by the inability to focus; therefore self-identified as a failure. Yet here I am, 40 years old, professionally and financially successful, artistically trained and skilled, and most importantly happy. In this book, I reflect on why I failed so much at certain elements of my life. I forgive my former self for how I erred as a son, brother, partner and friend.

Step into the world of best-selling children's book author Gavin Clifton as his inspirational story takes you on a journey of early battles, trials, achievements, and profound lessons learned along the way. Through his own eyes, Gavin uses his own words and unfiltered narrative to tell you of the many different experiences he's faced while navigating through life with cerebral palsy and a speech impediment.

How does an Unlikely Triathlete continue to exercise during a global pandemic? All this whilst being the Head of Fundraising for an NHS charity? It seems impossible doesn't it? Yet, Deborah continues with her tenacity to keep going as an athlete in the virtual world.

This narrative nonfiction novel chronicles my son’s twenty-year journey to get his Cushing’s disease diagnosed—a journey that took far too long. Throughout the book, I highlight opportunities for testing that could have been done according to endocrinologist guidelines. The core message is clear: early diagnosis is crucial for people to live vibrant lives.

After a normal, healthy, full-term pregnancy, Margaret Moore's parents Anne and Terrence were shocked as a prolapsed umbilical cord left their daughter unable to breathe on her own. Margaret, nicknamed Meg, was not expected to live through the night and began to breathe on her own by the next day—a phenomenon that medical personnel deemed a miraculous recovery. Meg came home with a physical disability Cerebral Palsy and permanent dependence on others for help with feeding, dressing, hygiene, and transfers to and from her wheelchair and walker.