Tourette Syndrome Research Support: New Centers and Data Collection
This act aims to expand and coordinate Tourette syndrome research by the National Institutes of Health. This means more funding for understanding the causes, diagnosis, and treatment of this condition, as well as improved data collection on its incidence and impact on citizens' lives. Specialized research centers will be established to conduct studies and inform about participation opportunities.
Key points
Increased funding and coordination for Tourette syndrome research, potentially leading to better treatment methods.
Creation of a system to collect data on Tourette syndrome in the U.S., including the availability of medical and social services.
Establishment of 4 to 6 specialized research centers in different regions of the country to conduct research and inform patients about participation opportunities.
Expired
Additional Information
Print number: 117_S_2027
Sponsor: Sen. Menendez, Robert [D-NJ]
Process start date: 2021-06-10