The Sickle Cell Disease Association of America, based in Atlanta, GA, is a national nonprofit organization dedicated to advocating for individuals affected by sickle cell disease. With a focus on education, research, and advocacy, the association provides resources and support to empower those living with the condition.
Through initiatives such as clinical trial finders, mental health campaigns, and community health worker training, the organization strives to improve the quality of life for sickle cell warriors and raise awareness about the disease. With a history spanning over 50 years, the SCDA advocates for advancements in treatments and access to care for individuals and families impacted by sickle cell disease.
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