Sickle cell disease (SCD) is a genetic condition that affects approximately 100,000 people in the United States and millions more globally. Individuals with SCD endure the psychological and physiological toll of repetitive pain as well as side effects from the pain treatments they undergo. Some adults with SCD report reluctance to use health care services, unless as a last resort, due to the racism and discrimination they face in the health care system. Additionally, many aspects of SCD are inadequately studied, understood, and addressed. Addressing Sickle Cell Disease examines the epidemiology, health outcomes, genetic implications, and societal factors associated with SCD and sickle cell trait (SCT). This report explores the current guidelines and best practices for the care of patients with SCD and recommends priorities for programs, policies, and research. It also discusses limitations and opportunities for developing national SCD patient registries and surveillance systems, barriers in the healthcare sector associated with SCD and SCT, and the role of patient advocacy and community engagement groups.
My Friend Chantal Has Sickle Cell Disease
Sickle Cell and Thalassaemia: Achieving Health Gain : Guidance for Commissioners and Providers
La drépanocytose est une maladie héréditaire de l'hémoglobine. En France, la drépanocytose est devenue l'une des premières maladies génétiques par le nombre de malades qui en sont atteints.
This edition of The Management of Sickle Cell Disease (SCD) is organized into four parts: 1. Diagnosis and Counseling 2. Health Maintenance 3. Treatment of Acute and Chronic Complications 4. Special Topics.
This book is available in print here for convenience. It is also available as a free download at http://www.nhlbi.nih.gov/health-pro/guidelines/sickle-cell-disease-guidelines/
All the while, exhaustion was her constant companion. Living with Sickle Cell Disease: The Struggle to Survive is a story of Judy Gray Johnson's perseverance in the face of living with a little-understood chronic illness.
Describes what scientists currently know about the relationship between genes and sickle cell disease, touching on technologies and experimental methods.
Report to the NHS Sickle Cell & Thalassaemia Screening Programme: Analytical Report on the Feasibility of Using Ethnic Questions for...
Depuis que le Dr Herrick, en 1910, a mis en évidence l'existence d'une anémie sévère, liée à une constitution particulière du globule rouge, l'exploration scientifique de la drépanocytose a traversé tout le siècle et progressé ...
Osaik is an eight-year-old boy. He is charming and has an unusual ability to hear things no one else hears. His world is thrown into disarray when a debilitating disease takes his mother from him.