Sickle Cell Genetics Project
        
     
    
        
    
    
        Project Description:
        Establish a follow-up component of Arkansas' sickle cell disease screening program, including community-based hemoglobinopathy counseling, education and support services.
Goals and Objectives:  The project goal is to improve the lives of children and families affect by sickle cell disorders through newborn screening follow-up and referrals, education, and family support.  The objectives are to improve the lives of children with sickle cell and their families by:  a) expanding the newborn screening follow-up to include education about sickle cell trait and hemoglobinopathy testing to 500 families of children born with sickle cell trait each year; b) training 70 health care professionals each year; c) providing sickle cell disease education to 500 persons annually; and d) offering family support to 100 families annually
     
    
        Keyword(s):
        sickle cell,  genetics,  education,  infants,  counselors
     
    
        Core Function(s):
        Performing Technical Assistance and/or Training, Developing & Disseminating Information
     
    
        Area of Emphasis
        Health-Related Activities
     
    
        Target Audience:
        Students/Trainees (long or intermediate trainees), Community Trainees / Short term trainees, Professionals and Para-Professionals, Family Members/Caregivers, Adults with Disabilities, Children/Adolescents with Disabilities/SHCN, Legislators/Policy Makers, General Public
     
    
        Unserved or Under-served Populations:
        Racial or Ethnic Minorities, Disadvantaged Circumstances, Geographic Areas, Rural/Remote, Specific Groups
     
    
        Primary Target Audience Geographic Descriptor:
        State
     
    
    
        COVID-19 Related Data:
        
                N/A