Our Problem
Sickle cell disease (SCD) is an inherited disease and one of the most neglected diseases in the world. SCD has plagued African children for over 8,000 years. The disease causes recurrent excruciating pain and disabling strokes; most affected children die early in childhood. About 300,000 children (85 percent of the global incidence) are born with the disease in Africa annually.
In Western countries, proven interventions dramatically reducing suffering and deaths from SCD are medically simple: infant screening, childhood vaccinations, a daily penicillin pill for five years, and lifelong daily pill of hydroxyurea to reduce sickling of blood cells. In Africa, a tiny minority of affected children receive care at tertiary hospitals, most of them after suffering severe irreversible complications such as brain strokes.
Access to largescale public health SCD care is urgently needed in Africa but has not materialized. Current programs are too slow and unaffordable.