Grief Illness

When Mark Doty went looking to adopt a small dog, a cuddly creature who might comfort his terminally ill partner, Wally Roberts, he was surprised to find himself returning home from an animal shelter with a full-grown golden retriever, a dog whose "absolute openess of regard", and paw gently offered through the bars of a cage, proved irresistable to him.

“Where is the handbook for widows?” Mary Kenyon lamented as she planned a funeral for the beloved husband whose triumph over cancer she chronicled in Chemo-Therapist: How Cancer Cured a Marriage. During the ensuing weeks, as she attempted to make sense of his untimely death, she filled two journals, blogged, and read the inspirational writings of others who had gone down the road of grief before her.

When Jarrett J. Krosoczka was in high school, he was part of a program that sent students to be counselors at a camp for seriously ill kids and their families. Going into, Jarrett was worried: Wouldn't it be depressing, to be around kids facing such a serious struggle? Wouldn't it be grim?

I met Amber when I moved across the street from her. As I got to know her, I learned some things about myself. My goal in writing this book is to help anyone that is going through the loss of a loved one or has lost someone. This is not just my own personal journey through grief, but a message of hope and love and a love that survived beyond death. This book is a memoir of personal reflections of the beginning, middle, and end of a soulful relationship between two women and a connection which brought about valuable lessons from love, life, grief, and letting go.

Wie können wir Hoffnung schöpfen und Kraft finden, wenn wir mit Krankheit, Kummer, Schmerz oder Tod konfrontiert sind? Diese Frage beschäftigt auch Julia Baird, als sie schwer an Krebs erkrankt. Im Phänomen der Phosphoreszenz findet sie schließlich die geeignete Metapher für das, was uns in dunklen Stunden Licht bringt: So, wie es die Phosphoreszenz Glühwürmchen, Quallen und sogar ganzen Ozeanen ermöglicht, aus sich selbst heraus zu leuchten, können auch wir Menschen unsere eigene Phosphoreszenz erschaffen.

Memoirs of a caregiver turned cancer patient, turned professional athlete: A young widow suddenly must raise three children alone - all while living with a rare blood cancer and working full time. This situation might make any woman despair, but Sally Kalksma is not just any woman. With her passion for life and her infectious energy, she found the motivation to power through adversity with tenacity and grit while never giving up hope, even when life looked its bleakest.

Nicky, a witty, intelligent, and clever 13-year-old, was diagnosed with a rare childhood bone cancer. However, this book is about more than cancer and its treatment and the fight to survive. It's about more than a mother and her son who accepted his mortality at such a young age and the strength and love between two loving souls.

In 1985, when Cindy Weinstein was a graduate student at UC Berkeley, her beloved father, Jerry, was diagnosed with early-onset Alzheimer's disease. He was 58 years old. Twelve years later, at age 70, he died having lost all of his memories, along with his ability to read, write, and speak.

Podróż na południowe krańce Europy jest klamrą, w której Wojciech Czuchnowski, znany dziennikarz i publicysta, pomieścił intymny pamiętnik o odchodzeniu swojej żony. Z wnikliwością, precyzją i bez znieczulenia prowadzi nas przez stadia miłości, kryzysów ich związku i choroby. Ta książka jest w równym stopniu bolesna, jak i niosąca nadzieję.

Sometimes, we need a reminder to help us keep a tight hold on this hope that we have in the promises of Christ, in spite of the suffering that is happening all around us, which, at times, closely touches even our families in this present world. Birthed from the desire to encourage a family member who was in stage four of a battle with cancer; and then, directly behind that, facing the unexpected death of a parent, Jodi L. Serino-Barbour reaches into the core of fear and pain to plant seeds of hope for the future.

Jesse Cooper was an honor-roll student who loved to windsurf and write poetry. He also had severe cerebral palsy and was quadriplegic, unable to speak, and wracked by seizures. He died suddenly at age 17. In fiercely honest, surprisingly funny, and sometimes heartbreaking prose, Jesse's mother, Marianne Leone, chronicles her transformation by the remarkable life and untimely death of her child.