What We Do
Programs &
Services
SCDF offers a range of programs and services to support individuals and families affected by sickle cell disease. Our programs include medical and educational support, counseling, and financial assistance. We also conduct research to further our understanding of sickle cell disease and to improve treatment options.
An education and support program specifically for parents of children with sickle cell disease.
BabySteps Parent Education Program
(Ages 0-6)
A creative outdoor group experience for children with sickle cell disease. Group activity, campfire programs, and community living.
Camp Crescent Moon (Ages 7-14)
Teens and Young Adults with sickle cell disease between the ages of 15-20 are eligible to attend. Camp activities include Archery, Zipline, Ropes Course, and more!
Camp Gibbous
(Ages 15-20)
Programs for Infants + Parents
Newborn Screening Hemoglobin Trait Follow-Up
The Sickle Cell Disease Foundation (SCDF) is a certified sickle cell trait counseling center. In partnership with the California Department of Public Health, Division of Genetic Disease Screening-Newborn Screening Program the SCDF provides parents of infants identified with sickle cell trait, hemoglobin C trait and hemoglobin D trait FREE trait counseling and family testing.
Clinical services specifically tailored to meet the needs of adults with sickle cell disease.
Adult Clinics
FREE counseling services are available at the Foundation. If you need help, we have experts available who understand how SCD affects individuals & families.
Psychosocial Support / Counseling
