We’re committed to the communities we aim to serve. In order to realize that commitment, we constantly strive to become more educated on sickle cell disease (SCD) and beta-thalassemia, and the experiences and journeys of the community. Through lunch and learns with individuals living with SCD and beta-thalassemia, community-based organizations (CBOs) and key SCD and beta-thalassemia opinion leaders, our team strives to understand the journey, challenges and opportunities for the community to provide a stronger foundation for our work each day.
Imara team commemorating Rare Disease Day
Craig Butler, National Executive Director of the Cooley’s Anemia Foundation speaking about Beta-thalassemia
Team members chatting with Mary Brown, President & CEO at Sickle Disease Foundation