The author shares her insights and perspectives on living with ALS, or Lou Gehrig's disease, sharing both her thoughts on life and happiness as well as practical ideas for daily living with this progressive neuromuscular disease.

Learn how a thirty-five-year-old fast rising, no nonsense Special Agent of our government turned a diagnosis of certain death into a life saving experience. A.L.S., It Literally Saved My Life author Dennis Eldridge delicately weaves his daily battle for life over death while exposing some of Satan's most prized secrets. Readers will both laugh and cry as they root for a man whose vocabulary doesn't contain the word quit. Readers will also greet with open arms and receptive hearts the bold manner in which author Dennis Eldridge systematically speaks truth into a world infiltrated by myths and dastardly lies from the 'evil one'. A.L.S., It Literally Saved My Life is a long overdue book that individuals should have at their fingertips.

​"The Only Way to Live" is a quick read filled with many entertaining stories. Michael has not held back anything in this book - brutal honesty and vulnerability when he talks about going from a life of non-stop adventure to his latest challenge of life - fighting ALS. An amazing tale of a kid with all the odds against him, moving all over the country multiple times with multiple family members in and out of his life, growing up and working hard to get what he wants in a career. Throughout the childhood stories, his young adult escapades, and through his years starting his career, it is apparent that Michael lives life to the fullest!​

Filled with intrigue and juicy stories, Nancy Hillis: The Vamp of Savannah tells the story of one of Savannah’s most colorful characters, Ms. Nancy Hillis. Now with ALS, Miss Hillis is telling the real story of Mandy Nichols, her character in the best selling book, Midnight in the Garden of Good and Evil. From her partnership with the piano playing, loving scoundrel Joe Odom in Sweet Georgia Browns, the hot jazz club in Savannah, Georgia; to her escapades with Minerva, the Voodoo Priestess; to her reign as a national beauty queen; and her heartbreaking dealings with the molestation of her son; Nancy tells it all—the good and not so good. You will laugh, cry and be amazed to read the story of this remarkable woman whose motto is “never, never, never give up.”

THE STORY: The time is 1919, a period of limited prosperity for Japanese families toiling in the sugarcane fields of the Hawaiian islands. Yachiyo, a young peasant girl, is destined for life in the fields and for a marriage to Willie, a lowly worke

The first three StarCraft novels--"Libertys Crusade, Shadow of the XelNaga, Speed of Darkness"--and the eBook "Uprising" are collected in this single volume, making this an essential tome for the millions of StarCraft game players.

“My dad was going to die. My sweet, loving, caring, and wonderful-in-every-way dad was going to leave me before he could watch my sister and me grow up.” At the tender age of fifteen, Sarah Caldwell learned that her father had been diagnosed with ALS (amyotrophic lateral sclerosis) and had only a short time left to live. In moments her life went from texting friends, going to gymnastics practice and family vacations by the sea to watching her father’s rapid, irreversible deterioration, a process that plunged her into deep depression. But Jim Caldwell was a man whose indomitable spirit in the face of his suffering provided the ultimate inspiration for Sarah to transform her depression into a journey of healing and love. She learned to accept her and her father’s fate and became determined not to waste a moment of the time she had left with him. When her father passed away, leaving Sarah to face life without her beloved dad, she was determined again to continue on the path of hope and strength, making sense of her loss and honoring his life by helping raise awareness of ALS and money for desperately-needed research for a cure. With a special foreword by former pro-football player Steve Gleason, Just To Make You Smile is the rare, honest, compassionate and bold account of a young adult’s process of watching a parent get ill and die, and the inspiration she hopes to impart by sharing her grieving process, deep inner growth and healing. By telling her story in its entirety, from the lowest depths of grief and depression to the heights of finding her inner strength, making a difference and carrying on her father’s fighting spirit, she hopes to touch the lives of others, especially kids with a sick parent, letting them know they are never alone on this difficult journey.

"'I was alone on that icy cold December day when I received my worst news in 2014... I went for that definitive test, and I wasn't the least bit prepared to be diagnosed with an incurable disease... I didn't know what to do with a prognosis of just a few years to live, growing more and more disabled until I could no longer move, swallow and, ultimately, breathe. I looked for a book that would guide me through this process. I wondered what to expect, how to share this news with colleagues, kith, and kin. Would I get angry? Sad? Depressed? How long would I remain in denial? But I never did find that book. Instead, I began writing it.' Norm MacIsaac writes in the opening of The Best of the Worst News. Written over several years as the disease progressed, the author explores living with amyotrophic lateral sclerosis (ALS), commonly referred to as Lou Gehrig's disease. This is a series of intertwined autobiographical tales set in over a dozen different countries spanning nearly half a century. It's not about the disease, but the emotional and psychological journey that accompanies such an earth-shattering diagnosis. Travel with him around the world and back in time as he tells stories of the people and places that inspired him to defy this incurable, degenerative disease, to embrace a positive perspective and live every day to the fullest."--

The time has come to tell my ALS reversal story. I have been silent long enough. In 2006 I was diagnosed with ALS and given 18 months to get my affairs in order. My physical condition deteriorated rapidly, until wheelchair-bound, I was only able to move my head and two fingers. My story is one of heartache, despair, the wish to end my life, and the Supernatural Gift of recovery. This book chronicles my journey and recovery as a rare ALS reversal. I feel I am in a unique position to offer solace and the understanding that only comes from enduring this disease. My Reversal taught me to never give up HOPE