Self-care management is an important part of living with a chronic illness. Sickle cell disease (SCD) is a chronic disease with acute, painful exacerbations that often results in a shortened life expectancy. Some middle-aged and older adults with SCD lived with the disease prior to having a diagnosis and without modern advances. The purpose of this study is to share the self-care recommendations of middle-aged and older adults with SCD. Using descriptive qualitative methods, data were gathered through semistructured interviews from 11 individuals living with SCD, including 6 women and 5 men. Self-care recommendations themes included physiological, psychological, and provider-related. The self-care recommendations may be seen as an additiona...
Sickle cell disease is characterized by acute pain crises. Pain, chronic medical problems, utilizati...
Background Transitions from paediatric to adult health-care ser...
Presentation given at the American Public Health Association (APHA) Annual Conference. Objective: S...
Sickle cell disease (SCD) is a genetic disorder which affects thousands of Black Americans. SCD is f...
SOJNR, issue 3, vol. 7, p.2 Background: Sickle cell disease (SCD) and its manifestations often resul...
Abstract Sickle cell disease is the most common genetic disorder in the United States. Approximatel...
Self-care is an important aspect of managing a chronic disease. In sickle cell disease (SCD), home s...
Background. Patients with SCD now usually live well into adulthood. Whereas transitions into adultho...
Exploring Telemedicine and Self-Management Practices of Transitioning Adults with Sickle Cell Diseas...
Aim of study To survey the self-medication practices of adults with Sickle Cell Disease (SCD) using ...
This article summarizes the psychometric evaluation of the Chronic Illness Assessment Interview for ...
Sickle Cell Disease (SCD) is an inherited blood disorder that affects 80,000 individuals in the Unit...
In individuals with sickle cell disease (SCD), recognizing the cues to an acute pain episode and res...
Background: Theories of self-care management, particularly the development of self-efficacy or confi...
Sickle cell disease (SCD) is the commonest inherited haemoglobinopathy worldwide. Although it is a c...
Sickle cell disease is characterized by acute pain crises. Pain, chronic medical problems, utilizati...
Background Transitions from paediatric to adult health-care ser...
Presentation given at the American Public Health Association (APHA) Annual Conference. Objective: S...
Sickle cell disease (SCD) is a genetic disorder which affects thousands of Black Americans. SCD is f...
SOJNR, issue 3, vol. 7, p.2 Background: Sickle cell disease (SCD) and its manifestations often resul...
Abstract Sickle cell disease is the most common genetic disorder in the United States. Approximatel...
Self-care is an important aspect of managing a chronic disease. In sickle cell disease (SCD), home s...
Background. Patients with SCD now usually live well into adulthood. Whereas transitions into adultho...
Exploring Telemedicine and Self-Management Practices of Transitioning Adults with Sickle Cell Diseas...
Aim of study To survey the self-medication practices of adults with Sickle Cell Disease (SCD) using ...
This article summarizes the psychometric evaluation of the Chronic Illness Assessment Interview for ...
Sickle Cell Disease (SCD) is an inherited blood disorder that affects 80,000 individuals in the Unit...
In individuals with sickle cell disease (SCD), recognizing the cues to an acute pain episode and res...
Background: Theories of self-care management, particularly the development of self-efficacy or confi...
Sickle cell disease (SCD) is the commonest inherited haemoglobinopathy worldwide. Although it is a c...
Sickle cell disease is characterized by acute pain crises. Pain, chronic medical problems, utilizati...
Background Transitions from paediatric to adult health-care ser...
Presentation given at the American Public Health Association (APHA) Annual Conference. Objective: S...