Georgia House Bill HB336

Georgia 2025-2026 Regular Session

• Introduced: 2/6/25

Caption

Education; local school systems to provide certain information to parents and guardians of students in grades six through twelve on sickle cell disease; require

Impact

If enacted, HB336 will amend existing educational regulations in the state of Georgia, particularly concerning health information sharing in schools. The bill will mandate local boards of education to include specific details about sickle cell disease in their communications with parents, thereby promoting greater awareness and facilitating timely medical consultations. The bill aims to improve health outcomes for affected students and ensure that they receive early intervention and the necessary support from healthcare professionals.

Summary

House Bill 336 aims to enhance the health education provided to parents and guardians of students in grades six through twelve by including critical information about sickle cell disease. Whenever local school systems disseminate health information—such as details on immunizations or medications—they will also be required to provide a comprehensive overview of sickle cell disease, which includes a description, risk factors, warning signs, and screening processes. This initiative intends to ensure that parents are adequately informed about the disease and can seek appropriate care for their children if necessary.

Contention

While the bill is primarily aimed at improving student health education, it could lead to debates surrounding the adequacy of resources and the training required for school systems to deliver this information effectively. Education advocates may express concerns about the implementation process, including how well local school systems can adapt to these new requirements. Additionally, discussions may arise concerning the broader implications of educational mandates on local education budgets and resources.