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1,816
result(s) for
"Breast Cancer Psychological aspects."
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After the Cure
by
Saskia Subramanian
,
Emily K. Abel
in
Antineoplastic agents
,
Antineoplastic agents -- Side effects
,
Breast
2008,2010
2009 Choice Outstanding Academic Title 2009 Association of American University Presses Award for Jacket Design Chemo brain. Fatigue. Chronic pain. Insomnia. Depression. These are just a few of the ongoing, debilitating symptoms that plague some breast-cancer survivors long after their treatments have officially ended. While there are hundreds of books about breast cancer, ranging from practical medical advice to inspirational stories of survivors, what has been missing until now is testimony from the thousands of women who continue to struggle with persistent health problems. After the Cure is a compelling read filled with fascinating portraits of more than seventy women who are living with the aftermath of breast cancer. Emily K. Abel is one of these women. She and her colleague, Saskia K. Subramanian, whose mother died of cancer, interviewed more than seventy breast cancer survivors who have suffered from post-treatment symptoms. Having heard repeatedly that \"the problems are all in your head,\" many don't know where to turn for help. The doctors who now refuse to validate their symptoms are often the very ones they depended on to provide life-saving treatments. Sometimes family members who provided essential support through months of chemotherapy and radiation don't believe them. Their work lives, already disrupted by both cancer and its treatment, are further undermined by the lingering symptoms. And every symptom serves as a constant reminder of the trauma of diagnosis, the ordeal of treatment, and the specter of recurrence. Most narratives about surviving breast cancer end with the conclusion of chemotherapy and radiation, painting stereotypical portraits of triumphantly healthy survivors, women who not only survive but emerge better and stronger than before. Here, at last, survivors step out of the shadows and speak compellingly about their \"real\" stories, giving voice to the complicated, often painful realities of life after the cure. This book received funding from the Susan G. Komen Foundation.
The undying : pain, vulnerability, mortality, medicine, art, time, dreams, data, exhaustion, cancer, and care
\"A ... meditation on data, pain, time, and the limited capacity of literature to comprehend life and death in a sensate and vulnerable body\"-- Provided by publisher.
Meeting Psychosocial Needs of Women with Breast Cancer
by
National Cancer Policy Board (U.S.)
,
Institute of Medicine (U.S.)
,
Herdman, Roger
in
Breast
,
Breast -- Cancer -- Patients -- Services for
,
Breast -- Cancer -- Psychological aspects
2004
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 research and proposes policies to improve the quality of care and
quality of life for women with breast cancer and their families. Because cancer of the
breast is likely a good model for cancer at other sites, recommendations for this cancer
should be applicable to the psychosocial care provided generally to individuals
with cancer. For breast cancer, and indeed probably for any cancer, the report finds
that psychosocial services can provide significant benefits in quality of life and success
in coping with serious and life-threatening disease for patients and their families.
The bright hour : a memoir of living and dying
\"Built on her ... Modern Love column, 'When a Couch is More Than a Couch' (9/23/2016), a ... memoir of living meaningfully with 'death in the room' by the 38-year-old great-great-great granddaughter of Ralph Waldo Emerson--mother to two young boys, wife of 16 years--after her terminal cancer diagnosis\"-- Provided by publisher.
Taking charge of breast cancer
by
Julia Ericksen
in
Breast
,
Breast -- Cancer -- Patients -- Interviews
,
Breast -- Cancer -- Psychological aspects
2008
Vividly showcasing diverse voices and experiences, this book illuminates an all-too-common experience by exploring how women respond to a diagnosis of breast cancer. Drawing from interviews in which women describe their journeys from diagnosis through treatment and recovery, Julia A. Ericksen explores topics ranging from women's trust in their doctors to their feelings about appearance and sexuality. She includes the experiences of women who do not put their faith in traditional medicine as well as those who do, and she takes a look at the long-term consequences of this disease. What emerges from her powerful and often moving account is a compelling picture of how cultural messages about breast cancer shape women's ideas about their illness, how breast cancer affects their relationships with friends and family, why some of them become activists, and more. Ericksen, herself a breast cancer survivor, has written an accessible book that reveals much about the ways in which we narrate our illnesses and about how these narratives shape the paths we travel once diagnosed.
The Wounded Breast
2001,2002
This is a rare multicultural perspective on disease, particularly cancer, in which the author takes on a journey through the medical establishments, cultural taboos, gender-tagged attitudes and personal stories of different civilisations. It could also be defined as a quest on how human logic relates to illness. The writing itself blends the diary, personal letters, poems and songs with excerpts from some of the foremost authorities in cancer research, producing an effect upon the reader akin to that which she experienced herself, as she moved back and forth between the emotional and physical shock of the cancer experience and the objective scientific data she uncovered. She begins to find cancer everywhere in her physical environment: friends, relatives and people she has never met -- some die. She finds a depth of friendship and support that she had never expected including that of her close companion. While writing her book she sent sections of it to friends, who commented on the text. These honest responses to her story add a further dimension. The structure and content of the book are informed by her deep commitment to women, men, ecology and peace issues. As part of the journey she reads many books on the environment and cancer. Although she lives in the USA and France, the book takes the reader on physical journeys to many other cities including Paris, Tunis and Beirut.
Coping with Breast Cancer
2008
This couples-focused group program aims to improve a couple's functioning as a \"team\" and provides a supportive environment for couples facing breast cancer-related issues. Over the course of six sessions, couples learn support and communication skills, as well as techniques to manage stress and enhance intimacy. Modeling by group leaders and other couples facilitates skill acquisition. With continued use, the skills learned in group can have long-term benefits for couples.
Psychological Aspects to Consider in Breast Cancer Diagnosis and Treatment
by
Colloca Giuseppe
,
Valentini Vincenzo
,
Dinapoli Loredana
in
Breast cancer
,
Cognitive ability
,
Post traumatic stress disorder
2021
Purpose of ReviewBreast cancer (BC) is the most common cancer diagnosed in women in the West World. Coping with cancer is cause of extreme stress for patients and their family. The purpose of this review is to evaluate possible approaches to follow to control those situations that can impact on quality of life (QoL) and compliance to treatments.Recent FindingsAnxiety, distress, depression, and posttraumatic stress disorder are the most frequent psychological disorders in BC patients. Cognitive disorders and sexual dysfunction can also be important in affecting QoL both in younger and older patients. Younger and older patients show different characteristics of these disorders and different strategies of managing them.SummarySeveral psychotherapeutic and supportive approaches have proven effective in managing psychological disorders in BC patients. Every BC patient should be supported with these techniques during her entire oncological history, in order to increase QoL and compliance to treatments.
Journal Article