What We Do
Uplifting Sickle Cell Disease as a Statewide Priority
As part of the Networking California for Sickle Cell Care Initiative, we are working to ensure that all Californians impacted by SCD are able to receive the quality health care they need and deserve.
Decades of inadequate funding for California adults living with SCD resulted in this underserved community dying at younger ages and at higher rates. Californians with SCD have higher incidents of emergency room visits and hospitalizations than patients in other states.
For the first time in California’s history, the governor committed $15 million statewide for sickle cell screening and treatment programs throughout the state.
This program marks the first time California has ever provided funding for SCD, which is the world’s most common genetic disease affecting approximately 100,000 in the U.S. alone. This initiative will help train physicians, as much as it will treat patients, to ensure those with SCD receive a timely diagnosis and the best care possible.
How we help
Programs + Services
Free services for persons with sickle cell disease, their families, and the general public.
Education + Training
The Sickle Cell Disease Foundation is State-Approved Sickle Cell Counseling Program.
Fundraising
Make a difference: make a donation or become a sponsor.