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Cancer Care in Countries and Societies in Transition
This is a rare compilation of clinically focused chapters on the practice of oncology in more than 25 countries and areas around the world that experience ongoing or intensifying ethnic, religious, and nationalistic conflict. Each chapter is written by an internationally respected local physician or nurse. Topics include the relationship between local culture and the local practice of mainstream modern medicine, critical clinical issues faced by local physicians, and options for when and how to incorporate palliative care. The book ends with chapters on the United States’ current initiatives on promoting cancer care training in these regions, and another on clinical concepts for Western clinicians undertaking oncology practice in emerging countries. The audience includes oncologists around the world: those practicing medicine in similarly extreme circumstances; Western oncologists organizing or preparing for medical missions; and Western oncologists who wish to learn from the experiences of oncologists who practice under radically different conditions.
Palliative Care for Chronic Cancer Patients in the Community
The new global cancer data suggests that the global burden has risen to 18.1 million new cases per year and 9.6 million cancer deaths per year. A number of factors appear to be driving this increase, in particular, a growing and aging global population and an increase of exposure to cancer risk factors linked to social and economic development. For rapidly-growing economies, the data suggests a shift from poverty- or infection-related cancers to those associated with lifestyles more typical in industrialized countries. There is still large geographical diversity in cancer occurrence and variations in the magnitude and profile of the disease between and within world regions. There are specifi...
Global Perspectives in Cancer Care
"Contemporary medical models focus predominantly on the technical and financial aspects of care. While these are important aspects of care, they fail to include what may be the most critical need of patients and families - that is, the whole-person approach to care where psychosocial and spiritual needs are viewed as essential and just as important as the physical. Cecily Saunders, the founder of hospice, was one of the first to describe the concept of 'total pain', which led to the biopsychosocial and spiritual model of care. In 2014, the World Health Assembly for the WHO passed a resolution which included spiritual care as an essential domain of palliative care, stating that Palliative Car...
The Impact of Culture and Faith in Dementia Care
This book provides the reader with a deeper understanding of the symptoms and palliative care needs of patients with dementia and their families. The book addresses the unique role of different cultures throughout the world and how this impacts psycho-social–spiritual healing. By looking at how patients with dementia are cared for in low-, middle-, and high-income countries, we can not only learn about cultures globally but learn from one another about unique and special models of care. Our hope is that by learning from different cultures, care for patients with dementia and their families will improve on a global scale. The book will be very useful for anyone involved in care for patients with dementia and their families, including neurologists, primary care physicians, psychiatrists, and physiotherapists, nurses, nurse practitioners, psychologists, spiritual ministry, social workers and volunteers.
Palliative Care
The incidence of cancer is alarmingly increasing worldwide. The major problem that the medical profession is currently facing refers to "late presentation" patients who, for the most part, have reached the terminal stage of the illness. For these people, the only treatment option left is palliative care. Various patterns of palliation have been in practice in every culture and in every ethnic group for generations. Unfortunately, we still lack significant and sustained investment in research related to the practice of palliative care. Authors from around the globe seek more investment of public and private funds to investigate ways to improve the bedside practice of palliative care. Modern p...
Palliative Care to the Cancer Patient
In the Middle East, as in other countries in the developing world, there is now a wide acceptance that palliative care is an important public health issue that should be integrated into the mainstream of cancer care as well as other life-threatening diseases. Nowadays, it is recognised as a human right issue that patients and families have the right to receive this care. The WHO defined palliative care as the active total care of the patient's body, mind and spirit; whereby health care providers need to evaluate and alleviate the patient's physical, psychological and social distress. Such care encompasses a broad, multidisciplinary approach that includes both the family and the community and...
Palliative Care -- Perspectives, Practices and Impact on Quality of Life
This book provides a new outlook on the practice of palliative care worldwide. All five continents are represented in this book by global leaders in this relatively new subspecialty. The chapters in the book re-emphasize the fact that in the 21st century, most patients in the world still lack this elementary tool to alleviate suffering physical, and even more so, emotional and spiritual which are so critical to people, especially when patients conditions become fatal. An issue that comes up again and again from almost all parts of the world, regardless of religion and traditional backgrounds, ethnicities, beliefs or faith, refers to the critical lack of basic and advanced training for physic...
Global Perspectives in Cancer Care
"Contemporary medical models focus predominantly on the technical and financial aspects of care. While these are important aspects of care, they fail to include what may be the most critical need of patients and families - that is, the whole-person approach to care where psychosocial and spiritual needs are viewed as essential and just as important as the physical. Cecily Saunders, the founder of hospice, was one of the first to describe the concept of 'total pain', which led to the biopsychosocial and spiritual model of care. In 2014, the World Health Assembly for the WHO passed a resolution which included spiritual care as an essential domain of palliative care, stating that Palliative Car...
The Bibliography of Australasian Judaica 1788-2008
This bibliography includes all traceable self-contained books, monographs, pamphlets and chapters from books which in some way pertain to Jews in Australia and New Zealand between 1788 and 2008 Born in Russia in 1942, Serge Liberman came to Australia in 1951, where he now works as a medical practitioner. As author of several short-story collections including On Firmer Shores, A Universe of Clowns, The Life That I Have Led, and The Battered and the Redeemed, he has three times received the Alan Marshall Award and has also been a recipient of the NSW Premier's Literary Award. In addition, he is compiler of two previous editions of A Bibliography of Australian Judaica. Several of his titles have been set as study texts in Australian and British high schools and universities. His literary work has been widely published; he has been Editor and Literary Editor of several respected journals and has contributed to many other publications.
