SCD (Sickle Cell Disease) Management

Sickle Cell Disease (SCD) management involves preventing and treating complications caused by abnormal hemoglobin in red blood cells. Key strategies include regular health check-ups, pain management during crises, staying hydrated, and taking medications like hydroxyurea to reduce sickling episodes. Patients are also monitored for infections, and vaccinations are important. In severe cases, blood transfusions may be needed to reduce abnormal cells. Lifestyle adjustments like good nutrition, avoiding extreme temperatures, and prompt treatment of infections help improve quality of life. Ongoing medical care aims to minimize symptoms, prevent organ damage, and manage complications effectively.