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Oncology and Palliative Social Work: Psychosocial Care for People Coping with Cancer illustrates the need for integrating early palliative care for patients with cancer and the important role social workers have in providing psychosocial support services across the cancer trajectory. There is a convergence of oncology and palliative social work specialties in the delivery of comprehensive, culturally-congruent, whole person cancer care. OPSW reflects the collective knowledge, skills, clinical experience and perspectives of a diverse group of interprofessional contributors, including best practices, emerging trends, and priorities in psychosocial oncology, and the impact of the COVID-19 pande...
This book addresses the unmet needs of the medical community in dealing with the psychological problems, particularly anxiety and depression, of patients diagnosed with cancer. Providing a scholarly review of the impact of cancer diagnosis on patients’ emotional and psychological status, as well as the evidence that psychological factors impact cancer occurrence and biological behavior, this book explores the therapeutic implications of such converse dynamics. Chapters review financial toxicity, eHealth, palliative care, mindfulness, sleep and cancer, social support and cancer, cultural diversity, pediatric and adolescent oncology, and geriatric oncology. While intended primarily for the p...
When Mom gets cancer all of the family's routines are disrupted, but with surgery, chemotherapy, radiation and rest, she eventually gets well enough to do the things they did before she got sick.
In Meeting Psychosocial Needs of Women with Breast Cancer, the National Cancer Policy Board of the Institute of Medicine examines the psychosocial consequences of the cancer experience. The book focuses specifically on breast cancer in women because this group has the largest survivor population (over 2 million) and this disease is the most extensively studied cancer from the standpoint of psychosocial effects. The book characterizes the psychosocial consequences of a diagnosis of breast cancer, describes psychosocial services and how they are delivered, and evaluates their effectiveness. It assesses the status of professional education and training and applied clinical and health services r...
Manual of Cancer Treatment Recovery guides the practitioner to understanding the issues involved in the care of cancer survivors. Manual of Cancer Treatment recovery teaches the practitioner how to guide patients and families in setting up and using a recovery plan; how to coordinate with other clinicians involved in the patient's management; and how to develop a directed survivorship program in their practice. Divided into three sections the book covers what one needs to know about survivorship, how to implement effective survivorship care, and how to work with patients utilizing the LEARN System (Living, Education, Activity, Rest, Nutrition), Dr. Fleishman developed. An appendix includes worksheet templates for the provider to give the patient to help in organizing and understanding the recovery plan.
"Learn to Live Through Cancer: What You Need to Know and Do" is the result of Dr. Stewart Fleishman's three decades of research, patient outreach and the development of his model of supportive integrative cancer treatment. The book presents a step-by-step guide to improve the length and quality of life for cancer survivors, helping them to manage the variety of physical, emotional, and spiritual issues they face proactively. In "Learn to Live Through Cancer: What You Need to Know and Do, " cancer survivors learn how to evaluate their condition, improve their communication with healthcare providers, research their illness and treatment options, seek complementary therapies when necessary, improve overall health habits, tend to their emotional well-being, and continue to monitor the long-term success of their survivorship program. The complete guide is an inspirational, cutting-edge book that provides a roadmap to a healthier and meaningful future following a cancer diagnosis.
This timely volume identifies factors that impede the success of women in STEM professions and demonstrates the negative impact of sexual harassment on women’s physical health, mental health, and job performance. Focusing specifically on the narratives of women in higher education, the authors illuminate the structural and systemic barriers facing women working as graduate students, faculty, and administrators. Drawing on insights from the #metoo and #timesup movements as well as the Brett Kavanaugh Senate hearings, this book: Provides real-life narratives as clarifying examples Validates the experiences of women struggling to negotiate the STEM workplace Recommends specific helpful practices for both women and employers .This book will be a valuable resource for those in academia and the workplace, and serve as an illuminating of women's experience generally.
William McGeorge was born in Scotland. He emigrated in 1793 with his second wife, Julie Hayden, and his son from his first marriage, John. They settled in Allegheny County, Pennsylvania. William and Julie had five children. Descendants and relatives lived mainly in Pennsylvania, Missouri, Kansas, Nebraska, South Dakota and California.
Prevention magazine provides smart ways to live well with info and tips from experts on weight loss, fitness, health, nutrition, recipes, anti-aging & diets.
The Oxford Textbook of Palliative Social Work is a comprehensive, evidence-informed text that addresses the needs of professionals who provide interdisciplinary, culturally sensitive, biopsychosocial-spiritual care for patients and families living with life-threatening illness. Social workers from diverse settings will benefit from its international scope and wealth of patient and family narratives. Unique to this scholarly text is its emphasis on the collaborative nature inherent in palliative care. This definitive resource is edited by two leading palliative social work pioneers who bring together an array of international authors who provide clinicians, researchers, policy-makers, and academics with a broad range of content to enrich the guidelines recommended by the National Consensus Project for Quality Palliative Care.