(a)    In this section, “Steering Committee” means the Statewide Steering Committee on Services for Adults with Sickle Cell Disease.
    (b)    There is a Statewide Steering Committee on Services for Adults with Sickle Cell Disease.
    (c)    The Steering Committee shall include representatives from:
        (1)    Local and national groups that advocate for individuals with sickle cell disease;
        (2)    Interest and support groups for individuals with sickle cell disease;
        (3)    Community and consumer groups;
        (4)    Academic and private clinical settings with knowledge and experience caring for adults with sickle cell disease;
        (5)    Area hospitals caring for individuals with sickle cell disease; and
        (6)    Pediatric clinics that care for children with sickle cell disease.
    (d)    The Steering Committee shall:
        (1)    Establish institution and community partnerships;
        (2)    Establish a statewide network of stakeholders who care for individuals with sickle cell disease;
        (3)    Educate individuals with sickle cell disease, the public, and health care providers about the State options for care of sickle cell disease; and
        (4)    Identify funding sources for implementing or supporting the actions, studies, policies, regulations, or laws recommended by the Steering Committee, including funding from:
            (i)    State, federal, and local government sources; and
            (ii)    Private sources.
Structure Maryland Statutes
Subtitle 5 - Sickle Cell Anemia
Section 18-501 - Intent of Subtitle
Section 18-502 - Test; Prenatal Education Program
Section 18-503 - Notice Requirements; Confirmatory Test
Section 18-504 - Confidentiality and Disclosure of Information
Section 18-505 - Blood Testing Procedure
Section 18-506 - Statewide Steering Committee on Services for Adults With Sickle Cell Disease