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sickle cell disease
It is estimated that SCD affects 90,000 to 100,000 people in the United States, mainly Blacks or African Americans.
Our commitment
​The EDS Sickle Cell Foundation wholeheartedly dedicates itself to uniting families through its family support services. These services are expertly crafted to heighten awareness of the disease and to enhance the quality of life by imparting knowledge, trauma-informed support, and empowering healing circles.
Mission
The EDS Sickle Cell Foundation, Inc., incorporated in 2022, is a non-profit organization based in Winston Salem, North Carolina. Its steadfast mission is to increase awareness and provide unwavering support to families affected by Sickle Cell Disease (SCD).
SUBSCRIBE
EDS Sickle Cell Foundation Inaugural EVENTS
5th Annual Sickle Cell WalkTime is TBDBuffalo
2nd Annual Inaugural Fire BallTime is TBDLocation is TBD
GIVE TODAY TO HELP A Family in need
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