Sickle Cell Disease Foundation

Founded in 1957, we’re the first and oldest non-profit, social service, sickle cell disease organization in the United States today. The Sickle Cell Disease Foundation has maintained a viable and reputable organization for over 60 years.

We address the needs of individuals with sickle cell disease and their families by emphasizing educational and support programs and services that meet the physical, psychosocial and economic needs of our clients.

With a growing population of individuals with sickle cell disease and sickle cell trait, a primary focus of the Sickle Cell Disease Foundation is to educate, screen and counsel those persons at risk of having children with sickle cell disease and other hemoglobin disorders.

Our mission is to build a world where individuals with Sickle Cell Disease get the care and compassion they deserve.