The public health response to COVID-19 has treated people with disabilities as disposable … [and] devaluation of people with disabilities has been our daily experience throughout this pandemic. 1T he coronavirus disease-2019 (COVID-19) pandemic arrived in 2020, at the 30th anniversary of the Americans with Disabilities Act (ADA). 2 Visible failures in our national response, and in the response of many social service and medical care organizations, leads many to question whether American society is living up to the original intent of the ADA. 3 The ADA guarantees individuals with disabilities equal access to employment, education, housing, transportation, telecommunications, government social services, and medical care. 2 Despite these guarantees and related efforts, individuals with disabilities had among the highest infection and death rates of any group during the COVID epidemic. Individuals with disabilities also faced a US health system that consistently made choices contrary to their best interests, and, in some instances, systems that proposed to allocate scarce life-saving treatments and rescue resources such as ventilators in actively discriminatory ways based on disability status. [4][5][6] As a result, more than 100 disability advocacy organizations across the nation penned a public letter, quoted above, to the Director of the Centers for Disease Control and Prevention (CDC) in 2022 requesting an apology from the federal government and an action plan to remedy systemic health inequities experienced by individuals with disabilities. 1 In this issue of Medical Care, Xie et al 7 report results from a nationally representative study of the US community-dwelling population that compared access to medical care for adults with versus without disabilities during the COVID-19 pandemic. The authors found that nearly 9% of adults reported severe disability limitations. Members of this group were 52% and 84% more likely to delay and forgo medical care, respectively, due to COVID-19, than were adults with no disability limitations. One-third of adults reported moderate disability limitations; this group was 33% and 46% more likely to delay and forgo medical care, respectively, due to COVID-19, than were adults without disability limitations. These findings were robust to adjustment for patient demographic, socioeconomic, regional market, insurance status, and other health condition risk factors.The study displayed many strengths, including the use of patient-reported data representing 250 million US adults in the National Health Interview Survey during the third and fourth quarters of 2020 after the onset of the pandemic, statistical adjustment of p values for multiple comparisons, and adjustment of point estimates for the potentially confounding patient risk factors described above. Given sample exclusion of institutionalized individuals receiving longterm care services, and given the role of disabilities and functional limitations as exogenous drivers of differences in patient socioeconomic and health risk factors...