Every Life Has Value Hunter Syndrome Awareness

Every Life Has Value Hunter Syndrome Awareness PDF Author: Eyasin Ali
Publisher:
ISBN: 9781702291538
Category :
Languages : en
Pages : 102

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Book Description
This beautiful Notebook For Women and Men To Write In and inspirational gift idea for Hospice Awareness Awareness patients and survivors to write down their Hospice Awareness Journey or to keep track of doctor's appointments, treatment. Writing is a great stress reliever, as well as a way to cope with your thoughts, feelings, and fears about Hospice Awareness. It will also give survivors a chance to look back on their journey and recall their fight. This journal will give patients motivation to keep going, never give up and never lose hope or faith. This blank lined notebook is a perfect gift for that special person battling Hospice Awareness.

Every Life Has Value Hunter Syndrome Awareness

Every Life Has Value Hunter Syndrome Awareness PDF Author: Eyasin Ali
Publisher:
ISBN: 9781702291538
Category :
Languages : en
Pages : 102

Get Book Here

Book Description
This beautiful Notebook For Women and Men To Write In and inspirational gift idea for Hospice Awareness Awareness patients and survivors to write down their Hospice Awareness Journey or to keep track of doctor's appointments, treatment. Writing is a great stress reliever, as well as a way to cope with your thoughts, feelings, and fears about Hospice Awareness. It will also give survivors a chance to look back on their journey and recall their fight. This journal will give patients motivation to keep going, never give up and never lose hope or faith. This blank lined notebook is a perfect gift for that special person battling Hospice Awareness.

Communities in Action

Communities in Action PDF Author: National Academies of Sciences, Engineering, and Medicine
Publisher: National Academies Press
ISBN: 0309452961
Category : Medical
Languages : en
Pages : 583

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Book Description
In the United States, some populations suffer from far greater disparities in health than others. Those disparities are caused not only by fundamental differences in health status across segments of the population, but also because of inequities in factors that impact health status, so-called determinants of health. Only part of an individual's health status depends on his or her behavior and choice; community-wide problems like poverty, unemployment, poor education, inadequate housing, poor public transportation, interpersonal violence, and decaying neighborhoods also contribute to health inequities, as well as the historic and ongoing interplay of structures, policies, and norms that shape lives. When these factors are not optimal in a community, it does not mean they are intractable: such inequities can be mitigated by social policies that can shape health in powerful ways. Communities in Action: Pathways to Health Equity seeks to delineate the causes of and the solutions to health inequities in the United States. This report focuses on what communities can do to promote health equity, what actions are needed by the many and varied stakeholders that are part of communities or support them, as well as the root causes and structural barriers that need to be overcome.

Parenting Matters

Parenting Matters PDF Author: National Academies of Sciences, Engineering, and Medicine
Publisher: National Academies Press
ISBN: 0309388570
Category : Social Science
Languages : en
Pages : 525

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Book Description
Decades of research have demonstrated that the parent-child dyad and the environment of the familyâ€"which includes all primary caregiversâ€"are at the foundation of children's well- being and healthy development. From birth, children are learning and rely on parents and the other caregivers in their lives to protect and care for them. The impact of parents may never be greater than during the earliest years of life, when a child's brain is rapidly developing and when nearly all of her or his experiences are created and shaped by parents and the family environment. Parents help children build and refine their knowledge and skills, charting a trajectory for their health and well-being during childhood and beyond. The experience of parenting also impacts parents themselves. For instance, parenting can enrich and give focus to parents' lives; generate stress or calm; and create any number of emotions, including feelings of happiness, sadness, fulfillment, and anger. Parenting of young children today takes place in the context of significant ongoing developments. These include: a rapidly growing body of science on early childhood, increases in funding for programs and services for families, changing demographics of the U.S. population, and greater diversity of family structure. Additionally, parenting is increasingly being shaped by technology and increased access to information about parenting. Parenting Matters identifies parenting knowledge, attitudes, and practices associated with positive developmental outcomes in children ages 0-8; universal/preventive and targeted strategies used in a variety of settings that have been effective with parents of young children and that support the identified knowledge, attitudes, and practices; and barriers to and facilitators for parents' use of practices that lead to healthy child outcomes as well as their participation in effective programs and services. This report makes recommendations directed at an array of stakeholders, for promoting the wide-scale adoption of effective programs and services for parents and on areas that warrant further research to inform policy and practice. It is meant to serve as a roadmap for the future of parenting policy, research, and practice in the United States.

Mother Power

Mother Power PDF Author: Jacqueline Hornor Plumez
Publisher: Sourcebooks, Inc.
ISBN: 1402252471
Category : Religion
Languages : en
Pages : 354

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Book Description
Through research and in-depth interviews with more than 50 women from all walks of life, Dr. Plumez found that "Mother Power" is changing society today, just as women's liberation changed it a few decades ago.

Chasing My Cure

Chasing My Cure PDF Author: David Fajgenbaum
Publisher: Ballantine Books
ISBN: 1524799629
Category : Biography & Autobiography
Languages : en
Pages : 256

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Book Description
LOS ANGELES TIMES AND PUBLISHERS WEEKLY BESTSELLER • The powerful memoir of a young doctor and former college athlete diagnosed with a rare disease who spearheaded the search for a cure—and became a champion for a new approach to medical research. “A wonderful and moving chronicle of a doctor’s relentless pursuit, this book serves both patients and physicians in demystifying the science that lies behind medicine.”—Siddhartha Mukherjee, New York Times bestselling author of The Emperor of All Maladies and The Gene David Fajgenbaum, a former Georgetown quarterback, was nicknamed the Beast in medical school, where he was also known for his unmatched mental stamina. But things changed dramatically when he began suffering from inexplicable fatigue. In a matter of weeks, his organs were failing and he was read his last rites. Doctors were baffled by his condition, which they had yet to even diagnose. Floating in and out of consciousness, Fajgenbaum prayed for a second chance, the equivalent of a dramatic play to second the game into overtime. Miraculously, Fajgenbaum survived—only to endure repeated near-death relapses from what would eventually be identified as a form of Castleman disease, an extremely deadly and rare condition that acts like a cross between cancer and an autoimmune disorder. When he relapsed while on the only drug in development and realized that the medical community was unlikely to make progress in time to save his life, Fajgenbaum turned his desperate hope for a cure into concrete action: Between hospitalizations he studied his own charts and tested his own blood samples, looking for clues that could unlock a new treatment. With the help of family, friends, and mentors, he also reached out to other Castleman disease patients and physicians, and eventually came up with an ambitious plan to crowdsource the most promising research questions and recruit world-class researchers to tackle them. Instead of waiting for the scientific stars to align, he would attempt to align them himself. More than five years later and now married to his college sweetheart, Fajgenbaum has seen his hard work pay off: A treatment he identified has induced a tentative remission and his novel approach to collaborative scientific inquiry has become a blueprint for advancing rare disease research. His incredible story demonstrates the potency of hope, and what can happen when the forces of determination, love, family, faith, and serendipity collide. Praise for Chasing My Cure “A page-turning chronicle of living, nearly dying, and discovering what it really means to be invincible in hope.”—Angela Duckworth, #1 New York Times bestselling author of Grit “[A] remarkable memoir . . . Fajgenbaum writes lucidly and movingly . . . Fajgenbaum’s stirring account of his illness will inspire readers.”—Publishers Weekly

Knowledge

Knowledge PDF Author:
Publisher:
ISBN:
Category : Science
Languages : en
Pages : 336

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Book Description


Genetic Knowledge of Human Values

Genetic Knowledge of Human Values PDF Author: Jacquelyn Ann Kegley
Publisher: Paragon House Publishers
ISBN:
Category : Medical
Languages : en
Pages : 296

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Book Description
Recent developments in the science of genetics and certain accompanying technologies promise the prevention and possible cure of disease. However, there are still many uncertainties about the application of genetic knowledge. There is, in fact, mounting evidence that our current models do not adequately describe our complex and flexible genetic mechanisms. The general lack of public understanding and over-expectation of the technological promise make ethical and public policy issues crucially important.This book addresses the many value, scientific, and public policy issues surrounding the use of genetic knowledge. From an interdisciplinary and multicultural perspective, the writers raise important questions about the definitions of health and disease; personhood and responsibility; discrimination, stigmatization, and the right of privacy. Also discussed are responsible, preventive medicine, and genetic carrier responsibility.

The Lancet

The Lancet PDF Author:
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 742

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Book Description


The Metabolic & Molecular Bases of Inherited Disease

The Metabolic & Molecular Bases of Inherited Disease PDF Author: Charles R. Scriver
Publisher: New York ; Montreal : McGraw-Hill
ISBN: 9780071363198
Category : Genetic disorders
Languages : en
Pages : 6338

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Book Description
Presents clinical, biochemical, and genetic information concerning those metabolic anomalies grouped under inborn errors of metabolism.

Dying in America

Dying in America PDF Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309303133
Category : Medical
Languages : en
Pages : 470

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Book Description
For patients and their loved ones, no care decisions are more profound than those made near the end of life. Unfortunately, the experience of dying in the United States is often characterized by fragmented care, inadequate treatment of distressing symptoms, frequent transitions among care settings, and enormous care responsibilities for families. According to this report, the current health care system of rendering more intensive services than are necessary and desired by patients, and the lack of coordination among programs increases risks to patients and creates avoidable burdens on them and their families. Dying in America is a study of the current state of health care for persons of all ages who are nearing the end of life. Death is not a strictly medical event. Ideally, health care for those nearing the end of life harmonizes with social, psychological, and spiritual support. All people with advanced illnesses who may be approaching the end of life are entitled to access to high-quality, compassionate, evidence-based care, consistent with their wishes. Dying in America evaluates strategies to integrate care into a person- and family-centered, team-based framework, and makes recommendations to create a system that coordinates care and supports and respects the choices of patients and their families. The findings and recommendations of this report will address the needs of patients and their families and assist policy makers, clinicians and their educational and credentialing bodies, leaders of health care delivery and financing organizations, researchers, public and private funders, religious and community leaders, advocates of better care, journalists, and the public to provide the best care possible for people nearing the end of life.