Cancer Caregiving A To Z Book in PDF, ePub and Kindle version is available to download in english. Read online anytime anywhere directly from your device. Click on the download button below to get a free pdf file of Cancer Caregiving A To Z book. This book definitely worth reading, it is an incredibly well-written.
Author : American Cancer Society Publisher : American Cancer Society Page : 0 pages File Size : 44,5 Mb Release : 2008 Category : Health & Fitness ISBN : 0944235921
Cancer Caregiving A to Z by American Cancer Society Pdf
"The role of caregiver in cancer care has expanded tremendously in recent years. People with cancer are living longer, and many cancer treatments once done in a hospital are now performed in an outpatient setting. In addition, hospital patients may be discharged early, often while they still are experiencing pain, discomfort, or other side effects from treatment. Caregivers at home suddenly have to perform tasks traditionally done by nurses, such as administering medications, monitoring symptoms, and hooking up intravenous antibiotics. Yet they have no formal training for the job. Whether the caregiver is a spouse, partner, adult child, or friend, this person fills an exceptional role--one the requires compassion and strength, as well as knowledge about health care issues. Cancer Caregiving A to Z was written by experts at the American Cancer Society to provide caregivers the knowledge they need to make the right decisions for loved ones who are recovering from cancer and the effects of cancer treatments"--Page 4 of cover.
The Comprehensive Guide to Cancer Caregiving: A Helping Hand For Patients, Caregivers, Family and Friends by C.L. Ueberroth Pdf
The book cancer patients and their families should receive upon diagnosis. Advise and help for cancer patients, caregivers, friends and family of cancer patients. Simple yet potent suggestions for caring for oneself or caring for someone else facing cancer. From the day of diagnosis on through all treatments, suggestions for physical symptoms, emotional strength, and day to day aspects of cancer treatment. A how to guide on dealing with today and preparing for tomorrow practically during cancer.
Things I Wish I'd Known by Deborah J. Cornwall Pdf
Family caregivers are the unsung heroes of the life-saving drama that's triggered by a cancer diagnosis. Nearly three quarters of American households will find themselves caring for a cancer patient at one point in their lives. This book is the first to capture their thoughts, feelings, and insights on a large scale. It is based on 101 formal interviews with non-professional caregivers (some of whom are cancer survivors themselves), covering 122 patients in 19 states and Canada who ranged in age from 2 to 92 and faced 40 different cancer diagnoses. Practical lessons drawn from caregivers' experiences are intermingled with their own words to forge a compelling narrative intended to help both patients and their family caregivers to understand and cope with the full range of issues they should anticipate as they fight the battle of their lives.
If cancer has touched your family, you need this book. The Cancer Caregiver Roles that have to be assumed are: 1) Medical Support-including scheduling, medication support, monitoring side effects, managing pain, maintaining medical records, and advance medical directives. 2) Insurance and Financial Management-selecting the right insurance plans, or finding resources if you have no insurance, and navigating the medical quicksand of costs so as not to drown in medical bankruptcy or lose your home. 3) Household Management-including nutrition management, safety, controls for infection, modesty, and physical/emotional/spiritual support. The final chapter of the book is on Laughter because splashes of laughter are a powerful antidote to pain, stress, and conflict. Laughter strengthens the body's immune system. Laughter pushes back the cancer for a while. The Epilogue deals with end of life.
Things I Wish I'd Known by Deborah J. Cornwall Pdf
Based on numerous interviews with cancer caregivers from across the United States, this comprehensive guide intersperses real-life stories with practical advice regarding the critical issues and decisions facing nonprofessional cancer caregivers. Topics range from logistical to medical to financial and emotional concerns in order to empower patients and caregivers on the cancer journey. A special chapter covers caring for children with cancer and how to best support children when another family member suffers from the disease. A must-read for all caregivers, irrespective of age, race, or economic status.
Informal caregivers - family members, friends, and other loved ones - are an essential, uncompensated and significantly burdened extension of the healthcare team. Rapid advances in cancer care, including new drugs and immunotherapies and more sophisticated diagnostic tools, have markedly improved the ability to medically extend lives and enhance survival. As patients are living longer, with today's shorter hospital stays and shift towards increased outpatient care, however, the demands placed on all caregivers and their needs have substantially increased. Cancer Caregivers reveals the field of Psycho-Oncology's exploration of the depth of complexities of caregiving experiences and identifies the vast expanses left to be understood. This text describes the characteristics and experiences of cancer caregivers based on their life stage, relationship to the patient, and ethnic group membership, as well as patients' disease and treatment type. It highlights the significant progress in research focused on the development and dissemination of psychosocial interventions for cancer caregivers, and includes in-depth case studies to illustrate their delivery and application. The text also explores the provision of support to caregivers in the community and the legal and ethical concerns faced by caregivers throughout the caregiving process. Cancer Caregivers offers both fundamental and practical information and is the essential resource for all healthcare professionals who work with patients and families facing cancer.
Hope an Inspiring A-Z Guide for Cancer Patients, Survivors and Caregivers by Patti McGee Pdf
Inspiring cancer survivors share their stories to assist newly diagnosed cancer patients, survivors and caregivers through their journey with cancer. Each story offers inspiration, hope and healing through journaling, health tips and support programs.
This guide is designed to walk you through the basics of cancer caregiving and provide practical tips and advice as well as useful resources from someone who has walked the walk of both patient and cancer caregiver. Conversation points throughout the guide will help you communicate with the patient and medical team.
Cocoon of Love for Cancer Caregivers by Susan Brownell Pdf
Rather than focus on how to perform hands-on caregiving, this book delves into practical ways to help the caregiver survive the emotional and physical impact of being a cancer caregiver. This book has many practical tips and suggestions which are certain to help any caregiver when caring for a loved one with a devastating illness. -- Amazon.
This book tells the story of a caregiver for a person who is seriously ill of cancer. It is of help to both the caregiver and the person suffering from illness. It offers physical, mental, emotional, and spiritual suggestions to help with the process of the disease, and, if it comes to that, dying. The book's information is valuable as a guide for any caregiver helping another with any serious, debilitating illness, not solely cancer. The large paperback is printed in a large font which allows for comfortable and fast reading. Caregivers, I know, are always pressed for time. Book Published March 25, 2005.
Author : Richard P. McQuellon,Michael A. Cowan Publisher : Oxford University Press Page : 161 pages File Size : 45,9 Mb Release : 2021 Category : Medical ISBN : 9780197500293
The Art of Conversation in Cancer Care by Richard P. McQuellon,Michael A. Cowan Pdf
"We use "mortal time" in our work to mean the experience of human beings confronting the prospect of death. This confrontation can stimulate intense feelings, a flurry of thoughts, and erratic or unusual behavior. In the broadest sense, mortal time is entered whenever death comes near, and that can happen either directly or vicariously. Hearing the words, "you have cancer," and signing a medical consent form where death is a possible medical "complication," are direct experiences of mortal time. Learning of a loved one's cancer diagnosis, losing a family member in an automobile accident, or reading about a missing child are vicarious experiences of mortal time. The power of tragedy in the theatre can brings us into the experience of mortality. King Lear's madness in the face of betrayal propels him toward an untimely death. The focus in this book is on the particular and powerful experience of entering mortal time when someone receives a diagnosis of cancer, a life-threatening illness. As we noted in our introduction to this second edition, the experience of mortal time in cancer medicine has changed with new treatments. A cancer diagnosis could mean an illness where rapid progression toward death is looming, or where there is only the distant possibility of death. Now there is a third option: the prospect of longer survival with metastatic disease due to the promise of additional therapies, facilitated by next generation genome sequencing. This means, a lengthier period of mortal time and uncertainty for many cancer patients. MORTAL TIME: HOW LONG DOES IT LAST? There are, of course, many instances in which people far exceed their statistically predicted life span. This holds true whether it be the prediction of a physician in the midst of treating an illness or the projected life span of an insurance life-expectancy table. In Part II we give an example of how misleading statistics can be when we discuss the idea of false hope. When mortal time looms with the diagnosis of cancer, it may stretch from days to years, with patients encountering both helpful treatments that lead to periods of remission and recurrences of disease requiring additional treatment. Some patients may never experience a time when it is apparent that they are dying until the last days. The interval between living and dying that we are concerned with here is not primarily chronological time, measured in days, weeks, and months. The hallmark of mortal time is the person's unique biological, psychological, social, and spiritual experience of the prospect and meaning of death, a prospect that confronts their caregivers as well. Mortal time is "kairos" time, the ancient Greek word meaning the time of decisions. When someone enters mortal time directly, their caregivers enter the same time zone vicariously. What they do together in mortal time, especially how they speak and listen to each other, affects the quality and meaning of life for all involved, in the moment and beyond"--
Author : National Cancer Institute (U.S.) Publisher : Government Printing Office Page : 28 pages File Size : 47,9 Mb Release : 2018-07-18 Category : Medical ISBN : 9780160947520
Caring for the Caregiver: Support for Cancer Caregivers by National Cancer Institute (U.S.) Pdf
Caring for the Caregiver is a booklet for people who are caring for a person with cancer. This booklet provides tips for helping you understand your feelings and asking for help, making time for yourself, caring for your body and spirit, going with your loved one to medical visits, and talking with friends and family members about cancer Related products: Children with Cancer: A Guide for Parents -- ePub format only -- ISBN: 9780160947537 Coping with Advanced Cancer: Support for People with Cancer -- ePub format only ISBN: 9780160947544 Eating Hints: Before, during and after Cancer Treatment -- ePub format only --ISBN: 9780160947551 Life After Cancer Treatment: Facing Forward -- ePub format only -- ISBN: 9780160947568 Pain Control: Support for People with Cancer -- ePub format only -- ISBN: 9780160947575 Radiation Therapy and You: Support for People with Cancer --ePub format only -- ISBN: 9780160947582 Surgery Choice for Women with DCIS and Breast Cancer -- ePub format only -- ISBN: 9780160947599 Taking Part in Cancer Research Studies --ePub format only -- ISBN: 9780160947605 Understanding Breast Changes: A Health Guide for Women --ePub format only -- ISBN: 9780160947612 Understanding Cervical Changes: A Health Guide for Women -- ePub format only -- ISBN: 9780160947629 When Cancer Returns: Support for People with Cancer -- ePub format only -- ISBN: 9780160947636 When Someone You Love Has Advanced Cancer: Support for Caregivers --ePub format only -- ISBN: 9780160947643 When Someone You Love Has Completed Cancer Treatment: Facing Forward --ePub format only -- ISBN: 9780160947650 When Someone You Love Is Being Treated for Cancer: Support for Caregivers --ePub format only -- ISBN: 9780160947667 When Your Brother or Sister Has Cancer: A Guide for Teens --ePub format only -- ISBN: 9780160947674 When Your Parent Has Cancer: A Guide for Teens -- ePub format only -- ISBN: 9780160947681
Cocoon of Love for Cancer Caregivers by Susan Brownell Pdf
At Last--Care for the Caregiver! Soon after you begin caring for your loved one with Cancer, you realize what an overwhelming commitment you have made. As you search for answers and understanding, you may feel alone and in need of someone to help you along. It seems others don't really understand what you are dealing with. You may even feel like it's all too much to bear. You have a lot of questions. This is not your usual caregiver book. "Cocoon of Love for Cancer Caregivers" will take you on the caregiver journey with compassion and practical tips to help both you and your loved one through this difficult time. It's a beautiful read with a heart-warming message of love for the caregiver. Within this book, you will discover - How to care for yourself at this challenging time How to make your loved one feel loved Ways to bring comfort, compassion, and joy into your daily lives What butterflies have to do with your loved one and you How to face your fears head on How to emerge from this experience a changed, but stronger person
