Our Services
Public Education
Formal presentations about sickle cell anemia and related hemoglobin abnormalities made to organizations, providers and other interested entities.
Professional - Teachers, Nurses, Physicians, Lawyers, other Health Care Providers.
General - Civic Associations, Sororities, Fraternities, Churches, Social Clubs, Parents
Community Screening Programs
Obtaining blood samples to determine hemoglobin status.
Mass Screening - Participating in health fairs, schools or other events where large attendance is expected.
Family/Individual - Families or individuals schedule appointments to have blood drawn or you may have a walk-in service.
Genetic Counseling Services
Providing scientific and genetic information regarding hemoglobinopathies.
Newborn Sickle Cell Disease - Counseling parents of children identified through the newborn screening program on the recurrence risks of having a child with Sickle Cell Disease.
Newborn trait - Counseling parents of children identified through the newborn screening program on the carrier status and probability of having a child with sick e cell trait/disease.
Family planning - Counseling couples at risk for having a child with Sickle cell Disease.
Trait - follow-up counseling for in house screening/testing services
Tutorial Services
Education assistance for children with Sickle Cell Disease.
Camp
Enrichment activities for children with Sickle Cell Disease (and their siblings).
Transportation
Allot funds to assist with transportation needs to and from medical appointments.
Support Networks
Organized groups of parents, teens and/or adults affected by sickle cell disease.
Regional Clinics
To provide professional support and assistance to UAB Division of Pediatric Hematology/Oncology by sponsoring children with sickle cell disease - ages infants to 18.
E-mail:
info@seasca.com 
