As a consequence, individuals with SCD live longer and are more prosperous than they were before.

The organization is working to meet the needs of patients, families, and populations impacted by Sickle Cell Disease by providing education, knowledge, and empathy in the United States and internationally. Creation and dissemination of instructional materials, granting of post-doctoral research fellowships, medical scholarships for sickle cell patients, patient advocacy services, and professional training and assistance by state, international, and local conferences are among the organization’s international programs. In over 300 counties throughout the United States and worldwide, the organization aims to have member groups offering various medical advocacy programs such as day camps, counseling, home treatment, and tutoring.