Bill > S2560

This bill aims to address and support research on Long COVID, which refers to health conditions that may result, directly or indirectly, from COVID-19 infection. The key provisions of the bill include: 1. Establishing a voluntary patient registry to collect data on Long COVID symptoms, treatments, and related information, while ensuring privacy protections and voluntary participation. 2. Requiring the Secretary of Health and Human Services to coordinate federal research and activities related to the long-term health effects of Long COVID, including conducting or supporting research and developing recommendations and educational materials for healthcare providers and the public. 3. Directing the Secretary to develop and disseminate public and provider education programs on Long COVID, including information on awareness, incidence, health effects, treatment options, and strategies for reducing the likelihood of developing Long COVID. 4. Authorizing $10 million per year from 2024 to 2028 to carry out the research activities outlined in the bill. The bill aims to improve understanding, diagnosis, and treatment of the long-term health effects associated with COVID-19 infection.

Health and Social Services

https://www.congress.gov/bill/118th-congress/senate-bill/2560/all-info