S 801

Comprehensive Access to Resources and Education for Long COVID Act or the CARE for Long COVID Act This bill requires research, education, and other activities to support individuals who have Long COVID or related conditions that may result directly, or indirectly, from COVID-19 infection. The Department of Health and Human Services (HHS) must support a voluntary patient registry to collect information about individuals with Long COVID and related conditions, such as their symptoms, treatments, and demographic characteristics. HHS must coordinate with the Patient-Centered Outcomes Research Institute on the registry. HHS must also conduct or support research along with other agencies on how the U.S. health care system responds to Long COVID and related conditions. This includes research on the effectiveness of treatments and strategies to mitigate disparities in health outcomes. In addition, HHS must (1) educate the public and health care providers about treatments for, conditions associated with, and other aspects of Long COVID and related conditions; and (2) disseminate information and resources on how Long COVID affects rights associated with employment, disability status, and education. Last, the Administration for Community Living must award grants to or enter contracts with states, health care providers, legal services providers, and other eligible entities for expanding access to legal assistance for individuals with Long COVID and related conditions, including assistance with obtaining Social Security and other benefits and accessing medical care and services.