Buch online Managing Sickle Cell Disease: In Low-Income Families (Health, Society, and Policy)

Beschreibung Managing Sickle Cell Disease: In Low-Income Families (Health, Society, and Policy)

/1592131956

Presents a comprehensive account of sickle cell disease (SCD) and its affect on low-income families. This book examines how low-income African American mothers with children suffering from this hereditary, incurable, and chronically painful disease, react to the diagnosis and manage their family's health care.

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Managing Sickle Cell Disease: In Low-Income Families on JSTOR ~ The off-handed statement that “kids do get sick” belies the difficulties experienced by the thirty-two low-income African American mothers in this study as they faced the consequences of having the sickle cell trait and passing a chronic illness, SCD, on to their children. A recent study of the impact of childhood SCD on Black families found that “when asked about it directly, there is .

Managing Sickle Cell Disease In Low Income Families Health ~ By Robin Cook - buy managing sickle cell disease in low income families health society and policy by hill shirley isbn 9781592131952 from s book store everyday low prices and free delivery on eligible orders managing sickle cell disease in low income families health society and policy by shirley a hill unknown edition get this from a .

Managing Sickle Cell Disease in Low-Income Families ~ Managing Sickle Cell Disease in Low-Income Families (Health, Society, and Policy) by Shirley A. Hill, unknown edition,

Managing Sickle Cell Disease: In Low-Income Families ~ Buy Managing Sickle Cell Disease: In Low-Income Families (Health Society And Policy) by Hill, Shirley (ISBN: 9781592131952) from 's Book Store. Everyday low prices and free delivery on eligible orders.

Managing Sickle Cell Disease: In Low-Income Families by ~ As many as 30,000 African Americans have sickle cell disease (SCD). Though the political activism of the 1960s and a major 1970s health campaign spurred demands for testing, treatment, and education programs, little attention has been given to how families cope with SCD. This first study to give.

American Society of Hematology 2020 guidelines for sickle ~ American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults M. R. DeBaun , M. R. DeBaun *

Reducing Health Care Disparities in Sickle Cell Disease: A ~ Community health workers who specialize in treating persons with SCD provide social support, offer informal counseling, and aid in navigating health systems. 25 The Sickle Cell Disease Association of America offers a certification program to expand the number of health workers qualified to support patients with SCD and has trained more than 300 health care workers (S. Fitzgerald, Community .

ASH Pocket Guides - Apps on Google Play ~ The ASH Pocket Guides app brings together all of ASH's pocket guides to provide guidance for the diagnosis and management of a variety of hematologic conditions. Key features include: New search and favorites features allow you to quickly access tools and guides you use regularly. Click the heart icon to elevate pocket guides or tools to the top of the list.

Reproductive Decisions in People With Sickle Cell Disease ~ The purpose of this analysis was to examine the beliefs, attitudes, and personal feelings of people with sickle cell disease or sickle cell trait related to making informed reproductive health decisions. Three focus groups were conducted with a total of 15 people who had either SCD or SCT. Five themes were identified: health-related issues in sickle cell disease, testing for sickle cell trait .

Sickle Cell Disease / NHLBI, NIH ~ The NHLBI offers many sickle cell disease resources, including publications and videos, to help patients, their families, and health professionals. Explore these resources to learn more about important topics, such as tips for healthy living, treatments, and managing pain. Some publications are also available in Spanish.

Helpline » Sickle Cell Society ~ Sickle Cell Society Helpline Do you have a sickle cell disorder or know someone who does? Are you looking for information, advice or support? The SCS Helpline Service provides confidential information, guidance, and emotional support to individuals and families affected by sickle cell living within the UK.

Overview / Sickle cell disease: managing acute painful ~ This guideline covers managing acute painful sickle cell episodes in children, young people and adults who present at hospital, from presentation until when they are discharged. It aims to reduce variation in how acute episodes are managed in hospital, focusing on effective, prompt and safe pain relief.

Sickle Cell Society - Supporting People Affected by Sickle ~ The Sickle Cell Society believes that individuals with sickle cell disorder have the right to quality care. This can only be achieved if funding is made available to educate health carers and other professionals about the condition. The Society aims to provide this. The Society does not discriminate between the types of sickle cell disorders or .

Sickle Cell Disease Monitoring / CDC ~ Sickle Cell Trait Toolkit is a collection of fact sheets covering various health problems affecting people with sickle cell trait. Stepping Up: A 2-part video series for teenagers and young adults with SCD. The videos share the stories of Kevin and Calvanay, two young adults with SCD, and their transition to adult care, how it has affected them .

Why self-care fails: Implementing policy at a low-income ~ Managing Sickle Cell Disease in Low-Income Families Philadelphia: Temple University Press. Google Scholar . Hopper, Susan. (1981). “Diabetes as a Stigmatized Condition: The Case of Low-Income Clinic Patients in the United States”Social Science and Medicine Vol. 15B: 11–19. Google Scholar. Katz, Alfred H and Lowell S. Levin (1980). “Self-Care IsNot A Solipsistic Trap: A Reply to Critics .

Paediatric to adult transition care for patients with ~ Sickle cell disease is a life-threatening inherited condition designated as a public health priority by WHO. Increased longevity of patients with sickle cell disease in high-income, middle-income, and low-income countries present unprecedented challenges for all settings; however, a globally standardised solution for patient transition from paediatric to adult sickle cell disease health care .