Your Advocates for Sickle Cell
SCDAA President and CEO Regina Hartfield visited Capitol Hill in Washington, D.C., to connect with federal lawmakers on SCDAA's legislative priorities, policy needs and other sickle cell priorities. We are proud to advocate for our community and are dedicated to this cause.
Become an advocate yourself and join us for the first-ever National SCD Policy Forum on March 21-22, 2023. This tri-collaborative event is hosted by SCDAA, Sick Cells and the Sickle Cell Community Consortium.