SICKLE CELL DISEASE FOUNDATION
Providing education and life-enhancing programs to individuals with sickle cell disease. The Sickle Cell Disease Foundation provides life-enhancing education, services, and programs for ind From healthcare to humancare, SCDF understands that sickle cell disease isn't just a health condition — it’s a human condition. One that requires genuine connection and a holistic lens that takes into account how the disease plays into our sense of self and belonging affects different areas of life, and relates to larger societal structures. Currently approximately 250 million people worldwide carry the gene responsible for sickle cell disease (SCD) and other hemoglobin diseases. Each year about 300,000 infants are born with a major hemoglobin disease worldwide. In the US, 10% of the population is at risk for SCD. It is estimated that there are approx. 5,000 persons with sickle cell disease in Los Angeles.
Founded
1957
2954
X (Twitter)
2063
Address
Ontario
Home | SCDF Website Translator SITE TRANSLATOR SERVING WITH CAREAND COMPASSION About SCDF The Sickle Cell Disease Foundation is a nonprofit organization that has been supporting individuals with sickle cell disease and their families since 1957. Sickle cell disease is an inherited disease in which a person does not have enough healthy red blood cells to carry oxygen throughout the body. What is Sickle Cell Disease. An initiative developed through advocacy and stakeholder engagement to uplifting Sickle Cell Disease as a statewide priority.
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SICKLE CELL DISEASE FOUNDATION
📢Join us for a free virtual session specifically designed for individuals and families affected by sickle cell disease. This Gene Therapy Educational overview will breakdown what gene therapy is, how it works, and what it could mean for the future of sickle cell treatment. Whether you’re curious, hopeful, or just want to learn more, this is a safe space to ask questions and hear from experts.
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