Sickle Cell Alliance Foundation

Launched in May 2014, Sickle Cell Alliance Foundation is a passionate non-profit, community-based organization. It is committed to being a valuable resource to guide and help families and patients – children, teens and adults – living with the life-threatening sickle cell disease. It’s goal is to ensure the appropriate programs and needed resources are available and offered to the patient and caregiver.

Through the strong connection with the families, Sickle Cell Alliance Foundation will be “their voice”. This will help as they advocate, partner and develop relationships with hospitals, schools, companies and public officials. This will help to heighten awareness and raise the much-needed funding to educate at the local and national levels to improve care.