Your Search Results

      • Trusted Partner
        The environment
        February 2007

        Greenhouse Gas Sinks

        by Edited by David Reay, Nick Hewitt, Keith A Smith, John Grace

        Bringing together leading researchers from around the world this book reviews how vegetation and soils act as naturally occurring buffers which use up the gases responsible for global warming and the greenhouse effect. It provides in-depth information on the importance of these sinks, how they may respond to increased greenhouse gas emissions, how we can protect them and how they can help us mitigate climate change.

      • Handicrafts, decorative arts & crafts

        Tiaras and Bridal Jewellery

        Projects Using Beads and Wire

        by Jema Hewitt

        Tiaras and Bridal Jewellery shows you how to make a special tiara for your wedding, prom or party. And how to create earrings, bracelets or a necklace to match. Professional costume designer Jema Hewitt shows how to make spectacular tiaras – funky or classic – all using beads and wire. And if you want to start designing your own tiaras, here are all the techniques you need. ‘very good value for money’ – The Beadworkers Guild Journal ‘versatile and useful’ – Bead magazine

      • Handicrafts, decorative arts & crafts
        August 2009

        Making Tiaras and Designer Jewellery

        by Jema Hewitt

        Make your own beaded tiara with matching designer necklace and earrings, for your wedding, prom or special party. In this ebook, Jema Hewitt shows you the techniques you need to create six stunning tiara and jewellery designs using beads and wire. There are tiaras to suit many tastes, from pastel and delicate, to bold and colourful. Follow Jema’s comprehensive step by step instructions, and zoom in close to see every detail of the construction. This is Jema’s second ebook on making tiaras after the success of Tiaras and Bridal Jewellery.

      • 2019

        The Ballad of Samuel Hewitt

        by Nick Tooke

        Set against the backdrop of the Great Depression, this story sees a young horse thief and his unlikely accomplice pursued through the forbidding landscape of the British Columbia Interior. There they encounter villains, drifters, and fiercely insular circus folk in a profound tale of friendship, forgiveness, and finding home.To learn more about this publisher, click here: http://bit.ly/2Y9PX2r

      • Early learning: first word books

        My Great Big Book of Everything

        by Angela Hewitt

      • Education

        Dewey and Power

        Renewing the Democratic Faith

        by Hewitt, R.

        Dewey and Power develops out of criticism that John Dewey’s work lacks a sufficient concept of power, thus rendering his faith in an amelioristic sense of experience and a democratic ideal untenable. According to philosopher Cornel West, Dewey gives ameliorism its most mature social, political, and ethical justification. Alan Ryan suggests that Dewey represented “thinking America” at its best. Dewey’s critics maintain, however, that this best is not good enough. If their criticism of Dewey goes unchallenged, one of the most intelligent, philosophically consistent visions of ethical behavior in a world shot through with difference, risk, danger, and change becomes damned. The upshot is lost faith in the idea that the give and take of mutual reference and pooled intelligence can lead to ever wider points of contact with each other that will enrich the significance of our individual quests together. Furthermore, lost faith in ameliorism and democracy implies a lost faith in a democratic education. The purpose of Dewey and Power, therefore, is to explore the diverse critiques of his alleged insufficient concept of power and to represent Dewey’s work in a way that his critics’ claims can be evaluated. The key word here is evaluate. The book is not a simple apology for Dewey’s position on these matters.First, the book works out Dewey’s concept of power as it comes out of his understanding of the psycho-physiological makeup of the human organism. Then the analysis of power as it is psycho-physiologically interpreted is extended to incorporate Dewey's ontological insights, especially that of the directing influence of social custom on habit. This process unveils a concept of power that includes both domination and liberation. Furthermore, the relation between Dewey's sense of power and his faith in a democratic ideal is drawn out in explicit detail. Next, the book provides a full delineation of Dewey’s critics’ claims and measures the worth of these claims in light of what the preceding examination suggests in reference to Dewey’s idea of power. This analysis makes clear that Dewey understood that power can be as productively oppressive as it can be productively liberating. Finally, the book traces out why Dewey's concept of power can be deployed in the construction of a critical, democratic education.

      • Working with Children Who Need Long-term Respiratory Support

        by Dr Jaqui Hewitt-Taylor

        This book discusses many of the day-to-day needs of children who require long-term respiratory support. This includes their physical requirements, but also their emotional, social and educational needs, and the needs of their families. The medical and technical aspects of these children’s care can seem overwhelming. However, arguably the more complex and challenging parts of their management concern things that are not directly related to their physical care, such as facilitating their social needs and education. This book aims to discuss all the aspects of care that such children and their families may need, and also to place these in the context of seeing the child as a whole person and as a part of society. To achieve this, six case studies of children who need long-term respiratory support are used throughout the book. CONTENTS: Why is this book needed? Getting to know children who require long-term respiratory support Why some children need long-term respiratory support Ways of providing respiratory support Assessing a child’s respiratory status Discharge planning Principles of working in the home setting Working with parents Working with the whole family Working with young people who require long-term respiratory support Children, families and loss Ethics and children’s rights

      • Children's & young adult fiction & true stories
        November 2014

        S.C.A.R.S

        by Julia Ibbotson

        Dragons, knights and a boy who slips through the fabric of the universe into a parallel fantasy medieval world to fight the evil Myrthor, the heart of darkness in the land of Unor.

      • Health systems & services
        November 2011

        Improving Health Literacy Within a State

        Workshop Summary

        by Maria Hewitt, Rapporteur; Roundtable on Health Literacy; Institute of Medicine

        Health literacy is the degree to which individuals can obtain, process, and understand the basic health information and services they need to make appropriate health decisions. According to Health Literacy: A Prescription to End Confusion (IOM, 2004), nearly half of all American adults--90 million people--have inadequate health literacy to navigate the healthcare system. To address issues raised in that report, the Institute of Medicine convened the Roundtable on Health Literacy, which brings together leaders from the federal government, foundations, health plans, associations, and private companies to discuss challenges facing health literacy practice and research and to identify approaches to promote health literacy in both the public and private sectors. On November 30, 2010, the roundtable cosponsored a workshop with the University of California, Los Angeles (UCLA), Anderson School of Management in Los Angeles. Improving Health Literacy Within a State serves as a summary of what occurred at the workshop. The workshop focused on understanding what works to improve health literacy across a state, including how various stakeholders have a role in improving health literacy. The focus of the workshop was on presentations and discussions that address (1) the clinical impacts of health literacy improvement approaches; (2) economic outcomes of health literacy implementation; and (3) how various stakeholders can affect health literacy.

      • Public health & preventive medicine
        February 2012

        Facilitating State Health Exchange Communication Through the Use of Health Literate Practices

        Workshop Summary

        by Maria Hewitt, Rapporteur;Roundtable on Health Literacy; Institute of Medicine

        Implementation of the Affordable Care Act (ACA) of 2010 will result in significant changes to the U.S. health care system. Among its many provisions, the ACA will extend access to health care coverage to millions of Americans who have been previously uninsured. Many of the newly eligible health insurance consumers will be individuals of low health literacy, some speakers of English and others more comfortable using languages other than English. Health insurance terms such as "deductible," "co-insurance," and "out-of-pocket limit" are difficult to communicate even to those with moderate-to-high levels of health literacy and so health exchanges will face challenges as they attempt to communicate to the broader community. In addition to having to convey some of these basic, and yet complex, principles of insurance, state exchanges will be attempting to adapt to the many changes to enrollment and eligibility brought about by ACA. The Institute of Medicine (IOM) convened the Roundtable on Health Literacy that brings together leaders from the federal government, foundations, health plans, associations, and private companies to discuss challenges facing health literacy practice and research and to identify approaches to promote health literacy in both the public and private sectors. The roundtable sponsored a workshop in Washington, DC, on July 19, 2011, that focused on ways in which health literacy can facilitate state health insurance exchange communication with potential enrollees. The roundtable's workshop focused on four topics: (1) lessons learned from existing state insurance exchanges; (2) the impact of state insurance exchanges on consumers; (3) the relevance of health literacy to health insurance exchanges; and (4) current best practices in developing materials and communicating with consumers. Facilitating State Health Exchange Communication Through the Use of Health Literate Practices summarizes the presentations and discussion that occurred during the workshop. The report provides an overview of health insurance exchanges, presents evidence on the extent to which consumers understand underlying health insurance concepts, and describes the relevancy of health literacy to health insurance reform and how health literacy interventions can facilitate the implementation of health insurance reforms. The report also provides a review of best practices in developing materials and communicating with consumers, and concludes with reflections on the workshop presentations and discussions by members of the roundtable and its chair. Further information is provided in the appendixes, the workshop agenda (Appendix A), workshop speaker biosketches (Appendix B), and testimony provided by the organization America's Health Insurance Plans (AHIP) (Appendix C).

      • Oncology
        March 2004

        Meeting Psychosocial Needs of Women with Breast Cancer

        by Maria Hewitt, Roger Herdman, and Jimmie Holland, Editors, National Research Council

        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.

      • Oncology
        May 2003

        Fulfilling the Potential for Cancer Prevention and Early Detection

        by Susan J. Curry, Tim Byers, and Maria Hewitt, Editors, National Research Council

        Cancer ranks second only to heart disease as a leading cause of death in the United States, making it a tremendous burden in years of life lost, patient suffering, and economic costs. Fulfilling the Potential for Cancer Prevention and Early Detection reviews the proof that we can dramatically reduce cancer rates. The National Cancer Policy Board, part of the Institute of Medicine, outlines a national strategy to realize the promise of cancer prevention and early detection, including specific and wide-ranging recommendations. Offering a wealth of information and directly addressing major controversies, the book includes: • A detailed look at how significantly cancer could be reduced through lifestyle changes, evaluating approaches used to alter eating, smoking, and exercise habits. • An analysis of the intuitive notion that screening for cancer leads to improved health outcomes, including a discussion of screening methods, potential risks, and current recommendations. • An examination of cancer prevention and control opportunities in primary health care delivery settings, including a review of interventions aimed at improving provider performance. • Reviews of professional education and training programs, research trends and opportunities, and federal programs that support cancer prevention and early detection. This in-depth volume will be of interest to policy analysts, cancer and public health specialists, health care administrators and providers, researchers, insurers, medical journalists, and patient advocates.

      • Oncology
        March 2006

        From Cancer Patient to Cancer Survivor - Lost in Transition

        An American Society of Clinical Oncology and Institute of Medicine Symposium

        by Maria Hewitt and Patricia A. Ganz, Editors, Institute of Medicine, National Research Council

        This report of the proceedings of a symposium held in conjunction with the release of the IOM report, From Cancer Patient to Cancer Survivor: Lost in Transition, represents an effort on the part of the American Society of Clinical Oncology (ASCO), the National Coalition for Cancer Survivorship (NCCS), and the Institute of Medicine (IOM) to further disseminate the findings and recommendations of the IOM report and to take the next step toward implementation of those recommendations. The symposium and this report serve as important vehicles to raise awareness, fill gaps that have existed in cancer patients' long-term care, and chart a course for quality care for cancer survivors and their families. More than 100 stakeholders in the cancer community, including survivors, advocates, healthcare providers, government officials, insurers and payers, and researchers participated in the symposium. This report culminates a series of work at the IOM focused on cancer survivorship. The idea to embark on a major study of cancer survivorship within the National Academies originated with the National Cancer Policy Board (NCPB). The NCPB was established in 1997 in the IOM and the National Research Council's Division of Earth and Life Studies at the request of the National Cancer Institute (NCI), the National Institutes of Health, and the President's Cancer Panel. The NCPB identified emerging policy issues in the nation's effort to combat cancer, and prepared reports that address those issues, including a series of reports on topics ranging from cancer prevention to end-of-life care.

      • Paediatric medicine
        September 2003

        Childhood Cancer Survivorship

        Improving Care and Quality of Life

        by Maria Hewitt, Susan L. Weiner, and Joseph V. Simone, Editors, National Research Council

        Only more recently has it been realized that the intense effort to care for and cure a child with cancer does not end with survival. Continued surveillance and a variety of interventions may, in many cases, be needed to identify and care for consequences of treatment that can appear early or only after several decades and impair survivors’ health and quality of life. The more than two-thirds of childhood cancer survivors who experience late effects -- that is, complications, disabilities, or adverse outcomes -- as a result of their disease, its treatment, or both, are the focus of this report which outlines a comprehensive policy agenda that links improved health care delivery and follow-up, investments in education and training for health care providers, and expanded research to improve the long-term outlook for this growing population now exceeding 270,000 Americans.

      • Oncology
        October 2000

        Enhancing Data Systems to Improve the Quality of Cancer Care

        by Maria Hewitt and Joseph V. Simone, Editors, National Cancer Policy Board, National Research Council

        One of the barriers to improving the quality of cancer care in the United States is the inadequacy of data systems. Out-of-date or incomplete information about the performance of doctors, hospitals, health plans, and public agencies makes it hard to gauge the quality of care. Augmenting today's data systems could start to fill the gap. This report examines the strengths and weaknesses of current systems and makes recommendations for enhancing data systems to improve the quality of cancer care. The board's recommendations fall into three key areas: Enhance key elements of the data system infrastructure (i.e., quality-of-care measures, cancer registries and databases, data collection technologies, and analytic capacity). Expand support for analyses of quality of cancer care using existing data systems. Monitor the effectiveness of data systems to promote quality improvement within health systems.

      • Oncology
        July 1999

        Ensuring Quality Cancer Care

        by Maria Hewitt and Joseph V. Simone, Editors; National Cancer Policy Board, Institute of Medicine and National Research Council

        We all want to believe that when people get cancer, they will receive medical care of the highest quality. Even as new scientific breakthroughs are announced, though, many cancer patients may be getting the wrong care, too little care, or too much care, in the form of unnecessary procedures. How close is American medicine to the ideal of quality cancer care for every person with cancer? Ensuring Quality Cancer Care provides a comprehensive picture of how cancer care is delivered in our nation, from early detection to end-of-life issues. The National Cancer Policy Board defines quality care and recommends how to monitor, measure, and extend quality care to all people with cancer. Approaches to accountability in health care are reviewed. What keeps people from getting care? The book explains how lack of medical coverage, social and economic status, patient beliefs, physician decision-making, and other factors can stand between the patient and the best possible care. The board explores how cancer care is shaped by the current focus on evidence-based medicine, the widespread adoption of managed care, where services are provided, and who provides care. Specific shortfalls in the care of breast and prostate cancer are identified. A status report on health services research is included. Ensuring Quality Cancer Care offers wide-ranging data and information in clear context. As the baby boomers approach the years when most cancer occurs, this timely volume will be of special interest to health policy makers, public and private healthcare purchasers, medical professionals, patient advocates, researchers, and people with cancer.

      • Health systems & services
        February 2013

        Oral Health Literacy

        Workshop Summary

        by Maria Hewitt, Rapporteur; Roundtable on Health Literacy; Board on Population Health and Public Health Practice; Institute of Medicine

        The Institute of Medicine (IOM) Roundtable on Health Literacy focuses on bringing together leaders from the federal government, foundations, health plans, associations, and private companies to address challenges facing health literacy practice and research and to identify approaches to promote health literacy in both the public and private sectors. The roundtable serves to educate the public, press, and policy makers regarding the issues of health literacy, sponsoring workshops to discuss approaches to resolve health literacy challenges. It also builds partnerships to move the field of health literacy forward by translating research findings into practical strategies for implementation. The Roundtable held a workshop March 29, 2012, to explore the field of oral health literacy. The workshop was organized by an independent planning committee in accordance with the procedures of the National Academy of Sciences. The planning group was composed of Sharon Barrett, Benard P. Dreyer, Alice M. Horowitz, Clarence Pearson, and Rima Rudd. The role of the workshop planning committee was limited to planning the workshop. Unlike a consensus committee report, a workshop summary may not contain conclusions and recommendations, except as expressed by and attributed to individual presenters and participants. Therefore, the summary has been prepared by the workshop rapporteur as a factual summary of what occurred at the workshop.

      • Oncology
        July 2001

        Interpreting the Volume-Outcome Relationship in the Context of Cancer Care

        by Maria Hewitt and Diana Petitti, Editors, National Cancer Policy Board, Division on Earth and Life Studies, National Research Council

        Interpreting the Volume-Outcome Relationship in the Context of Cancer Care is a summary of a workshop held on May 11, 2000, which brought together experts to review evidence of the relationship between volume of services and health-related outcomes for cancer and other conditions, discuss methodological issues related to the interpretation of the association between volume and outcome, assess the applicability of volume as an indicator of quality of care; and identify research needed to better understand the volume--outcome relationship and its application to quality improvement.

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