MS HB787

Creates the Concern for Children with Sickle Cell Disease Task Force to study the growing incidence of the disease and make recommendations to the Mississippi Legislature on identifying, treating, and accommodating individuals with the disease and their families.

Task force membership consists of 13 members including three parents of children with Sickle Cell Disease, representatives from the State Department of Education, State Department of Health, Sickle Cell Anemia Association, medical associations, University of Mississippi Medical Center, a pediatrician in private practice, and a licensed nurse.

Task force shall review best practices from other states regarding educational, medical, and support services for individuals with Sickle Cell Disease and assess current Mississippi school district and medical services.

Task force shall identify potential funding sources for school districts, develop educational guidelines, evaluate higher education's role in workforce development for Sickle Cell Disease services, and make legislative recommendations for a continuum of services.

Task force must hold its first meeting by April 1, 2010, and file a report with relevant legislative committees and state agencies by December 1, 2010; State Department of Health shall provide necessary staff and support.