At the Foundation for Sickle Cell Disease Research we believe that everybody is born with the right to a long, healthy, pain-free life. With innovative research, treatments, and education, we can change the conversation and shape the future for this genetic disorder.
JOIN THE FIGHT TO SHAPE THE FUTURE OF
SICKLE CELL DISEASE.
WHO WE HELP
Sickle cell disease patients and their families no longer have to suffer alone. Hear stories from real-life patients.
FUNDING RESEARCH
FSCDR works with countless research institutions to improve comprehensive standards of care and maximize the quality of life for those affected for generations ahead.
OUR SUPPORTERS
Compassionate collaborations make everything possible to improve the wellbeing of sickle cell patients.
OUR SERVICES
The nation’s first comprehensive multispecialty center dedicated to sickle cell patients provides long-term, holistic services for those affected. Get a free screening to know your status.
42-48 YRS
National median life expectancy
1-10
African Americans are born with SCD
15-16
years old sevenfold chance of death
1-5
Physicians feel comfortable treating SC patients
ONLY 2
FDA approved medications for SC
