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April 30, 2025
Quarterly Opinion
Sara Rosenbaum
Marc A. Cohen
Jane L. Tavares
Alison Barkoff
Apr 1, 2025
Feb 28, 2025
Feb 21, 2025
Back to The Milbank Quarterly Opinion
Since the Affordable Care Act (ACA) Medicaid expansion passed in 2010, Medicaid work requirement proponents have sought to convince policymakers that the Medicaid working-age adult population is dominated by young, “able-bodied” adults who simply don’t work. This assertion is contrary to a mountain of evidence showing that the vast majority of working-age adults (aged 18-64) insured through Medicaid are either working, caring for family members, or exempt because of health issues.
Nonetheless, these baseless claims persist. Using what the authors cite as “responsive records” supplied by 23 states, a new report from the Foundation for Government Accountability (FGA) argues that “most Medicaid beneficiaries do not work at all.” Legally, a “responsive record” is a term of art under the Freedom of Information Act meaning a “record provided by a government in response to an information request.” FGA provides no information regarding what kind of records they examined, how they were analyzed, or any other indication of their reliability or accuracy or even their relevance to the question of the work status of Medicaid beneficiaries.
The FGA study also fails to offer any insight into the real question: Who exactly are these “able-bodied” Medicaid-enrolled working-age adults who do not work, how many of these adults actually exist, and what are their characteristics?
This information is essential if the goal is a policy that promotes work and community engagement without punitive measures that fail to account for who the population is and wrongfully deprive people of access to health care. Overwhelming evidence shows what can happen under broad mandates that tie health care to compliance with work reporting: Affected people, including workers and potentially exempted people are unable to navigate the reporting maze, lose their health care, uninsurance rates rise, and employment rates don’t change.
To provide more detail regarding the question of who exactly are working-age, but nonworking, “able-bodied” Medicaid adults, we analyzed data from the 2023 American Community Survey (ACS), the Census Bureau’s gold standard annual population survey and the premier source of highly detailed information about Americans. The survey contains information collected from over 3.5 million households regarding multiple aspects of life, including income, health and health care, family and living arrangements, and work status.
Our focus was working-age adults who live in the community and who are enrolled in Medicaid. Within this population, we undertook three basic comparisons: (a) Medicaid enrollees versus their counterparts who are not enrolled in Medicaid; (b) Medicaid enrollees who work versus those who do not work; and (c) nonworking “able-bodied” Medicaid enrollees versus able-bodied enrollees who do, in fact, work. For the purpose of this analysis, we focused especially on the able-bodied question. We define the term “able-bodied” individuals as people who report no health issues, do not receive either Social Security Disability Insurance (SSDI) or Supplemental Security Income (SSI) because of disability, do not have dependents under 18, and are not currently attending school. These attributes basically describe the population of interest among Medicaid work mandate proponents.
Here is what our analysis revealed:
In sum, “able-bodied” adults are a small portion of working-age Medicaid enrolled adults ages 18 to 64. They are not healthy young adults just hanging out. Although they may not have current health problems, many are middle-aged women or older, and a quarter are older than 50. They are very poor, have limited education, the majority once worked, most have left the workforce, and now they care for family and cannot afford to lose their own health care.
The most recent iteration of a federal work mandate, the 2023 House-passed Limit Save Grow Act, aims to penalize states that are unable to get people like these women to work. The bill would claw back hundreds of billions of dollars over time from states unable to prove that their working-age population is either exempt or working. The proposal rests on an assumption that there are tens of millions of healthy working-age adults enrolled in Medicaid who could work and do not.
Our robust analysis of the gold standard ACS data tells a dramatically different story.
First, working-age adults who could be classified as “able bodied” because they report no health problems, no advanced disability, and no dependents at home, represent only one in seven working-age Medicaid adults.
Second, they are not young people who choose not to work. They are older women (26% over age 50) who once worked but left the workforce to stay home and care for family.
Third, they are very poor, with limited education. They are reaching the end of a job life. Given the demands and hardships they face, they have limited time, ability, or opportunity to transform themselves into dynamic workers earning decent wages with job-based health insurance. Finally, because they are older, they are entering a period of life when it is absolutely essential, given who they are and how much their families depend on them, that they not experience needless disruption in their health insurance in furtherance of a punitive, mandatory work policy bearing no relationship to reality. Moreover, from a purely federal budgetary perspective, it is vital to keep this group of people stably insured. Many will enter Medicare in the not-too-distant future, and the evidence shows that Medicare—and therefore American taxpayers—will bear the financial consequences of depriving this group of health care access now. We simply cannot afford a Medicaid work mandate that will do nothing to increase employment and only serves to disinsure vulnerable, impoverished older working-age women on whom their families depend.
Sara Rosenbaum, JD, is Emerita Professor of Health Law and Policy at George Washington University’s Milken Institute School of Public Health. Previously she served as the Harold and Jane Hirsh Professor of Health Law and Policy and as founding Chair of the Department of Health Policy.
Professor Rosenbaum has devoted her career to health justice for medically underserved populations. She is a member of the National Academies of Sciences, Engineering, and Medicine, served on CDC’s Director’s Advisory Committee and the CDC Advisory Committee on Immunization Practice (ACIP), and was a founding Commissioner of Congress’s Medicaid and CHIP Payment and Access Commission (MACPAC), which she chaired from January 2016 through April 2017.
Professor Rosenbaum is the recipient of many honors and awards, including the National Academy of Medicine’s Adam Yarmolinsky Medal, awarded for distinguished service to a member from a discipline outside the health and medical sciences; the American Public Health Association Executive Director Award for Service; and the Association of Schools and Programs of Public Health Welch-Rose Award for Lifetime Contributions to the Health of the Public.
Marc A. Cohen, PhD, is a professor of gerontology at UMass Boston and co-director of the LeadingAge LTSS Center @UMass Boston. He is also a research director at the Center for Community Engagement in Health Innovation at Community Catalyst. He receives research funding from the RRF Foundation for Aging. Prior to joining UMass in the fall of 2016, Cohen served as the chief research and development officer and former president and co-founder of LifePlans, Inc., a long-term care research and risk management company.
Jane Tavares, PhD, is a senior research fellow at the LeadingAge LTSS Center @UMass Boston and an associate lecturer in the Department of Gerontology at the University of Massachusetts Boston. She has extensive experience working with large-scale representative panel data, such as the Health and Retirement Study. Her research explores how social relationships and social factors are associated with various aspects of health. She receives research funding from the RRF Foundation for Aging. More recently, Dr. Tavares has undertaken research examining social inequities in the US health care system related to person-centered care and eligibility/access to government benefit programs. She has also conducted demographic research to identify US older adults who are most financially vulnerable and to explore related longitudinal predictors and risk factors for financial vulnerability in later life. Dr. Tavares is the former managing editor of the peer-reviewed journal Research on Aging.
Alison Barkoff, JD, is the Harold and Jane Hirsh Associate Professor and program director at the George Washington University Milken Institute School of Public Health. She is a nationally recognized expert on long-term services and supports (LTSS), disability and aging policy, health care, and civil rights, with more than 25 years’ experience leading legal and policy advocacy. Prior to joining George Washington University, Barkoff led the Administration for Community Living in the Department of Health and Human Services (HHS) from January 2021 to October 2024. She served as the HHS secretary’s adviser on aging and disability policy; oversaw national disability and aging programs; led interagency initiatives related to LTSS, family caregiving, direct care workforce, and housing; and led the development of regulations related to Medicaid LTSS, health care discrimination, aging programs, and elder justice. Earlier in her career, she served in leadership roles in the Civil Rights Division of the Department of Justice, Bazelon Center for Mental Health Law, and Center for Public Representation. Barkoff has testified before Congress and the US Commission on Civil Rights.