CARE for Long COVID Act

The CARE for Long COVID Act establishes a national patient registry to collect data on Long COVID symptoms, treatments, and demographic information to improve understanding of the condition. It allocates $30 million for the registry in 2024, $15 million for research on healthcare disparities related to Long COVID, and $30 million annually for public and provider education programs about symptoms and treatments. The bill also creates interagency coordination to inform people about their rights in employment, education, and disability benefits related to Long COVID, with $30 million annually for this purpose. Additionally, it provides $50 million annually to support legal and social services assistance for people with Long COVID seeking disability benefits, healthcare access, and other services. The bill directly affects individuals with Long COVID, healthcare providers, and legal service organizations by improving data collection, education, and access to support services.