The ER doctor said, “Let’s take a chest x-ray just to be safe.” The results were simple, the sentence easily stated, and the next time period of life was about to be defined. “There is a white spot on the top right lung. You’d better have your doctor look at this!” That spot turned out to be lung cancer, and with that diagnosis Jim and Betty Serritella began a journey of tests and treatment on the road to becoming cancer-free. Fighting and winning the battle with cancer is a long and arduous process. You need a team of doctors and nurses you can trust, friends and loved ones to provide support, and lots of prayer. The Journey Through Cancer is a road map of the process Jim and Betty followed to battle Betty’s lung cancer. Jim wrote this book to help provide guidance for those on their own cancer journey, especially the caregivers and patient advocates, and to share lessons they learned along the way. “The Journey is a heartfelt personal account of struggle through the diagnosis, treatment and recovery of cancer. This book is not an oncology textbook written by a medical expert. This is a user’s guide written by an experienced caregiver intended to help other patients, caregivers and “team members” get a better understanding and insight into this most challenging process.” Dr. Neil Farber, MD, PhD, Associate. Professor “This book offers great spiritual, medical and practical guidance for the cancer patient, caregiver, relative of patient, friend of patient, and those working on the patient’s prayer chain. Please read it, and remember how each of us being treated need those daily naps, good nights of sleep, and the knowledge that our loved ones are in our corner at all times, supporting our effort to battle the disease, with prayer, good wishes, humor and the occasional good meal.” Cancer survivor - Daniel M. Gray, Attorney at Law, Falls Church, VA Jim Serritella is veteran of the US Air Force, and he spent more than fifty years in the world of systems, computers, and consulting. He is a life member of the Disabled American Veterans, the American Legion Post 171 of Damascus, Maryland, and a fourth degree Knight of Columbus. His advice for those going through the cancer journey: Don’t stop asking questions. And don’t forget to pray for help and understanding in fighting a battle you cannot win alone.

I wrote this book for other women, newly diagnosed with breast cancer, who wondered exactly what they could expect from the treatment of the condition. It's an account of my experiences and emotions during the treatment.

Kate Hayward 'journeyed' from nurse to patient when she was diagnosed with grade three breast cancer. In this book she shares her experiences as both a carer and a patient, giving hope to those fighting the disease.

It is often said that bioethics emerged from theology in the 1960s, and that since then it has grown into a secular enterprise, yielding to other disciplines and professions such as philosophy and law. During the 1970s and 1980s, a kind of secularism in biomedicine and related areas was encouraged by the need for a neutral language that could provide common ground for guiding clinical practice and research protocols. Tom Beauchamp and James Childress, in their pivotal The Principles of Biomedical Ethics, achieved this neutrality through an approach that came to be known as "principlist bioethics." In Pastoral Aesthetics, Nathan Carlin critically engages Beauchamp and Childress by revisiting the role of religion in bioethics and argues that pastoral theologians can enrich moral imagination in bioethics by cultivating an aesthetic sensibility that is theologically-informed, psychologically-sophisticated, therapeutically-oriented, and experientially-grounded. To achieve these ends, Carlin employs Paul Tillich's method of correlation by positioning four principles of bioethics with four images of pastoral care, drawing on a range of sources, including painting, fiction, memoir, poetry, journalism, cultural studies, clinical journals, classic cases in bioethics, and original pastoral care conversations. What emerges is a form of interdisciplinary inquiry that will be of special interest to bioethicists, theologians, and chaplains.

Incurable disease is a natural phenomenon, inherent to the human condition. This book critically investigates the uniquely human experience of and response to illness and treatment, which affects the body, the mind, and the very core of human existence and identity. Uncertainties regarding the outcomes of laboratory and other investigations that aid in the diagnosis and assessment of disease exacerbate the apprehension inherent to the diagnosis of incurable disease. An excessively scientific approach may disregard the suffering patient. The book begins by analysing the nature, meaning and significance of hope in the context of disease, and goes on to reflect on the language of medicine and the role of emotion, ideology and politics in disease treatment and research. The epilogue reflects on healing as distinct from physical cures. Without hope, there is no future; without healing, no holistic recovery. The final chapters are devoted to the end-of-life period of this journey. This book is a revision, extension, and reconceptualization of the original Afrikaans publication Hoop, Heling en Harmonie: Dink Nuut Oor Siekte en Genesing, winner of the 2021 Andrew Murray Prize for Theological Publications.

Daniel Thomas was 17 when he was diagnosed with rare bone cancer. His chances of survival were slim. But his father David refused to give up hope and did everything in his power to find his son a cure. Sadly, Daniel didn't survive but this account of the journey is testament to a parent's unconditional love and mankind's desperate need for hope.

National Book Critics Circle Award Finalist A New York Times Notable Book of the Year "Transcendently disobedient, the most existence-affirming and iconoclastic defense a writer could mount against her own extinction." --Heidi Julavits, New York Times Book Review From "one of the great anomalies of contemporary literature" (The New York Times Magazine) comes a breathtaking memoir about terminal cancer and the author's relationship with Nobel Prize winner Doris Lessing. In July 2014, Jenny Diski was diagnosed with inoperable lung cancer and given "two or three years" to live. She didn't know how to react. All responses felt scripted, as if she were acting out her part. To find the response that felt wholly her own, she had to face the clichés and try to write about it. And there was another story to write, one she had not yet told: that of being taken in at age fifteen by the author Doris Lessing, and the subsequent fifty years of their complex relationship. In the pages of the London Review of Books, to which Diski contributed for the last quarter century, she unraveled her history with Lessing: the fairy-tale rescue as a teenager, the difficulties of being absorbed into an unfamiliar family, the modeling of a literary life. Swooping from one memory to the next--alighting on the hysterical battlefield of her parental home, her expulsion from school, the drug-taking twenty-something in and out of psychiatric hospitals--and telling all through the lens of living with terminal cancer, through what she knows will be her final months, Diski paints a portrait of two extraordinary writers--Lessing and herself. From a wholly original thinker comes a book like no other: a cerebral, witty, dazzlingly candid masterpiece about an uneasy relationship; about memory and writing, ingratitude and anger; about living with illness and facing death.