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Healthcare providers, researchers, and advocates
The Sickle Cell Association is a not-for-profit organization that strives to diminish suffering and improve the quality of life for those individuals affected by sickle cell disease. They are committed to raising the public’s awareness and providing education to patients, their families, health professionals, legislators and the general public about sickle cell disease, its management and its challenges.
Sickle Cell Association Mission is to support the sickle cell community while working to eliminate the disease through collaborations on research, education and resources.
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