Sickle Cell Disease (SCD) is a genetic disorder that affects millions of people around the world. It is characterized by abnormally shaped red blood cells that can cause a range of health problems, including pain crises, anemia, organ damage, and a decreased lifespan. It is a complex condition that requires comprehensive management strategies to improve the quality of life for those living with it.
SCD is a genetic condition that affects hemoglobin (the protein responsible for carrying oxygen in the red blood cells). Individuals with SCD have abnormal hemoglobin molecules that cause their red blood cells to become deformed and fragile. These deformed cells can clog blood vessels, leading to severe pain and a range of health complications.
Every contribution counts. By donating, you can support our efforts to provide essential services, education, and resources to individuals and families affected by health challenges.
Donate now