Legislation
- Title
- Sickle Cell Trait Screening, Treatment, Education, and Public Awareness (Journey's Law)
- Sponsored by
- Delegates Acevero, Washington, Anderson, B. Barnes, Boyce, Bridges, Carr, Charkoudian, Charles, Conaway, Crutchfield, Cullison, D.M. Davis, W. Fisher, Forbes, Fraser-Hidalgo, Gilchrist, Harrison, Haynes, Henson, Ivey, C. Jackson, M. Jackson, Kerr, Korman, R. Lewis, Lierman, Lopez, Love, Moon, Mosby, Palakovich Carr, Patterson, Qi, Queen, Rogers, Sample-Hughes, Smith, Stewart, Turner, Valentino-Smith, Wells, Wilkins, Williams, Pendergrass, Pena-Melnyk, Reilly, Kelly, Bagnall, Chisholm, Morgan, Hill, Krebs, Rosenberg, Bhandari, Kipke, K. Young, Szeliga, Barron, Johnson, Saab
- Status
- In the Senate - First Reading Education, Health, and Environmental Affairs
- Analysis
- Fiscal and Policy Note
Synopsis
Requiring the Statewide Steering Committee on Services for Adults with Sickle Cell Disease to work in conjunction with members of the medical community in leading a certain comprehensive education and treatment program; requiring the Maryland Department of Health, in conjunction with local health departments and the Steering Committee, to develop a public awareness campaign on the importance of an individual knowing one's sickle cell trait status, receiving screening for the sickle cell trait and counseling under certain circumstances; etc.
Committees
Committee Testimony
Details
Introduced in a prior session as: HB1414 Session: 2018 Regular Session
Bill File Type: Regular
Effective Date(s): October 1, 2020
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18-506 )
Last Updated: 9/22/2020 2:19 PM