Bill > H1443

This bill establishes a statewide Parkinson's disease registry and mandates reporting requirements for healthcare professionals to improve the understanding and care of Parkinson's disease and atypical parkinsonism, which are neurological conditions affecting movement. Beginning January 1, 2027, physicians and advanced practice registered nurses (APRNs) who diagnose or treat patients with these conditions must report specific information, including nationally recognized performance measures, to this registry. The bill also provides legal protection, stating that physicians and APRNs will not be held liable for damages for providing this information. Furthermore, it modifies the Parkinson's Disease Research Board by adding appointments from the President of the Senate and the Speaker of the House of Representatives, revising membership qualifications to include specialists in movement disorders and informatics or population health research, and adjusting term lengths. The University of South Florida's Institute for Parkinson's Disease, subject to funding, will be responsible for creating and maintaining the statewide registry and a dedicated public website by January 1, 2028, which will feature annual reports on disease incidence and prevalence, as well as other relevant information. The bill also requires annual reports from the board to the Governor and legislative leaders, which, starting in October 2028, will include detailed updates on Parkinson's disease statistics within the state. This act is set to take effect on July 1, 2026.

Budget and Finance, Health and Social Services

Health & Human Services Committee (House), Health Care Budget Subcommittee (House), Health Professions & Programs Subcommittee (House)

https://www.flsenate.gov/Session/Bill/2026/1443