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Book Three in the Intelligent Patient Guide series. All the information breast cancer patients need to take an informed and active role in their treatment.
This best-selling self-help book for cancer patients and their families, by five practising physicians and professors of medicine, is the definitive authority on all aspects of breast cancer. It equips patients with the knowledge needed to take an active part in their treatment. Patients involved in making decisions about their treatment are better able to deal with their illness than are patients who relegate control to their doctors. Topics covered in the book include what cancer is, all about mammograms, breast self-examination technique, risk, what to do if a lump is found, benefits and side effects of all treatments, chemotherapy and radiation, what type of surgery is best, coping with cancer, reconstructive surgery and physiotherapy, handling the emotional side, diet and vitamins, what herceptin is and how it should be used, the new concept of partial breast radiotherapy, what a sentinel node biopsy is, and practical tips on living with cancer.
This best-selling self-help book for cancer patients and their families, by five practicing physicians and professors of medicine from Toronto and Vancouver, is the definitive authority on all aspects of breast cancer. It equips patients with the knowledge needed to take an active part in their treatment. Patients involved in making decisions about their treatment are better able to deal with their illness than are patients who give control to their doctors. Topics covered in the book include what cancer is, all about mammograms, breast self-examination technique, risk, what to do if a lump is found, benefits and side effects of all treatments, chemotherapy and radiation, what type of surgery is best, coping with cancer, reconstructive surgery and physiotherapy, living with the diagnosis, diet and vitamins, what herceptin is and how it should be used, the new concept of partial breast radiotherapy, what a sentinel node biopsy is, preventing recurrence of cancer, and practical tips.
Discusses the causes and diagnosis of breast cancer, treatment options, breast reconstruction, chemotherapy, hormone therapy, radiation therapy, diet, and prevention
More and more women are searching the Internet for medical information. Women who have been diagnosed with breast cancer search for information and participate in online communities—groups that “gather” in established online spaces to interact about their diagnoses of breast cancer. They share their own struggles and emotions with their own language: the rhetoric of breast cancer. They ask questions, share experiences, create friendships, discuss their disease processes, and present their illness narratives. However, they also create ethical dilemmas for online researchers and privacy issues as they share information that is legally protected through HIPAA. Online communities will only increase as research of online information expands through big data and predictive analytics, and more than ever before, women need to be aware of the information they share. Researchers also need to be aware, as they share the data they gather, and seek to preserve the privacy of the creators of the online data that they investigate and report. The Rhetoric of Breast Cancer provides a discussion of the complex structures of online communities, particularly those focused on medical diagnoses, and is a valuable read for patients, theorists, physicians, and researchers.
Family & health.
Cancer Resources on the Internet shows cancer patients, their families, and oncology health care professionals how the Internet can be used to locate information about the diagnosis, treatment, and prognosis of different forms of cancer; to locate specialized treatment centers around the world; to facilitate support groups; and to provide a mechanism for individuals to share experiences and stories. This book includes a discussion of the quality of information on the Net (and how to assess it); evaluations of Web sites in terms of content, clarity, and user-friendliness; and advice on how to conduct a focused, subject-specific search. Arranged in an order that gives a general starting point and then leads to more specific needs, Cancer Resources on the Internet helps you by: providing an overview of cancer resources available on the WWW--how to overcome the sheer quantity of information and find the most relevant sites discussing the National Cancer Institute's CancerNet, including ways to access the network and links to other resources detailing OncoLink, the first multimedia cancer information resource on the Internet offering state- of-the-art, quality information reviewing NCI's comprehensive cancer center's 26 web sites--from patients’and referring physicians’viewpoints showing how to find information on breast cancer on the Internet--Web-based resources on risk factors, early detection, treatment, psychological aspects, and breast cancer in men discussing different types of Internet resources (mailing lists, newsgroups, and real-time communication) and using cancer information to show how health care information can be transferred from physician to patient and back again illustrating a practical use of Internet Relay Chat (IRC)--how it offers accessibility to shut-in and convalescing patients and instant, real-time support guiding you through the process a newly diagnosed Hodgkin's Disease patient might use to find information and support on the Internet reviewing resources found on the Web about alternative and complementary therapies for cancer Information resources on the Internet about cancer, from Web sites to listservs and chat groups, are plentiful. In fact, cancer patients and oncology health care professionals were some of the earliest users of the Internet as a health information resource. Using cancer as the focus of this book provides a helpful overview of the various health care uses of the Net.
This is an original sociological study of breast cancer patients' participation in Internet spaces. While much has been debated about the significance of the Internet, the actual processes of communication in which people engage online are little understood as yet. Exploring the ways in which participants in online spaces configure their experience into a story, the book presents readers with an innovative way of understanding online communication as a socially significant activity. The substantive focus of storytelling online is analyzed sensitively and thoroughly in its specificity as a social phenomenon. At the same time it is connected to a broad range of debates on communication and Internet, health, illness, and social agency.