Author(s): Christy Mallory and Will Tentindo, Williams Institute at University of California - Los Angeles

Article Type: Report 

This report highlights key factors related to Medicaid coverage of gender affirming care. Emphasis is placed on the sheer number of individuals who identify as transgender or gender non-conforming that are covered by Medicaid – about one fourth of those who identify as transgender or gender non-conforming in the United States rely on Medicaid for their gender affirming care. Underlying factors contributing to inequities for this group include unclear language about what services are covered, and/or gender affirming care services are not covered at all in their state. Authors urge all states to fully expand their Medicaid program under the Affordable Care Act. 

Author(s): Robin J. Kempf, Assistant Professor in the College of Public Service at the University of Colorado - Colorado Springs; Nicole M. Elias, Associate Professor in the Department of Public Management at John Jay College of Criminal Justice, City University of New York; Alonso J. Rubin-DeSimone, John Jay College of Criminal Justice, City University of New York

Article Type: Peer-reviewed journal 

This peer reviewed journal article describes how transgender and gender non-binary individuals have been marginalized historically in U.S. society, including in terms of institutional or informal “erasure” as well as through isolation and “hypervisibility.” In health care, this discrimination translates into lack of access to qualified professionals and lack of coverage for a continuum of needed services. Authors chose to review state Medicaid program coverage policies to identify opportunities to build equity for all U.S. residents and noted that discrimination of individuals identifying as non-cisnormative gender can be compounded by the intersectionality of race, sexual orientation, socioeconomic status, and geographical location. They assessed comprehensiveness of state Medicaid coverage in accordance with the World Professional Association for Transgender Health (WPATH) standards. Authors found that the five states in their sample varied widely in terms of health coverage to transgender and gender non-binary Medicaid beneficiaries, however, there were stand out states in terms of the continuum of services offered as well as opportunities for improvement. Authors recommend removal of barriers to needed care such as prior authorization requirements as well as additional training for providers and individuals making coverage determinations.

Author(s): Nance Yuan, Cedars-Sinai Transgender Surgery and Health Program, and member of the Urology and Plastic Surgery Divisions at Cedars-Sinai Medical Center; Theodore Chung, David Geffen School of Medicine, University of California, Los Angeles; Alma Jimenez-Eichelberger and Caitlin Sioni, Cedars-Sinai Transgender Surgery and Health Program and the Division of Urology at Cedars-Sinai Medical Center; Edward C. Ray, Division of Plastic Surgery, Cedars-Sinai Medical Center; Maurice M. Garcia, Departments of Urology and Anatomy, University of California, San Francisco 

Article Type: Peer-reviewed journal 

This peer reviewed article investigates and discusses insurance requirements for referral letters from mental health providers prior to genital gender affirming surgeries for trans and non-binary individuals. In this study, half of the participants had federally funded insurance, such as Medicaid. Most plans, both public and private, required at least two referral letters at every stage of surgery (there may be four to five stages depending on the operation). Authors state that it took office staff, “an average of 2.5 hours per patient, per surgery, dedicated to coordinating submission of updated referral letters”. Some participants had to cancel or reschedule an operation due to lack of coordination of care, and/or administration not receiving referral letters. This resulted in patients being forced to pay for surgeries out-of-pocket instead of using insurance coverage. The authors discuss how multiple letters for each stage of a surgery is unnecessary, when no participant was deemed mentally unfit for any previously performed procedure. Authors state that requiring updated letters for each year was also a point of stress for participants as these administrative burdens were “costly and burdensome” to patients and providers alike. The authors urge organizations such as the World Professional Association for Transgender Health (WPATH) to revisit their recommendations for referral letter requirements to alleviate the burdens on both administrators and patients alike.

Author(s): Samuel Mann, Christopher S. Carpenter, Benjamin Harrell, and Cameron Deal are all from the Department of Economics, LGBTQ+ Policy Lab, Vanderbilt University, Nashville, Tennessee; Gilbert Gonzales is also a member of the Department of Medicine, Health & Society, and Department of Health Policy at Vanderbilt University. 

Article type: Peer-reviewed journal 

This peer reviewed journal article analyzes how Medicaid expansion influenced health insurance coverage for individuals in same-sex partnerships. Using data from the American Community Survey, authors found that there was a significant increase in coverage between 2009 and 2018 for low-income adults who were in a same-sex relationship, especially for women. The authors attribute this to a much higher prevalence of children being in households of women same-sex couples compared to men. The authors also state that sexual minority women may have stronger social ties that reduce stigma surrounding Medicaid or public options compared to sexual minority men. This research has implications that are important for policymaking and underlying factors of inequity within Medicaid in terms of barriers to seeking health insurance coverage and accessibility of services for those individuals in same-sex partnerships. 

Author(s): Carli Friedman, Director of Research for The Council on Quality and Leadership (CQL) at the University of Washington; Laura VanPuymbrouck, Assistant Professor of Occupational Therapy at Rush University

Article Type: Peer-reviewed journal

This peer reviewed article summarizes findings from a quantitative study exploring the association between ableism in the U.S. and Medicaid spending on long term services and supports. It begins with historical context about deinstitutionalization of people with disabilities and the history of Medicaid as both a primary payer for long-term care and an insurer for people with disabilities. Despite research indicating community living has more benefits than institutions, investments in home and community-based services vary state to state; authors hypothesize that an association exists between stereotypical attitudes toward people with disabilities (i.e., as dependent, a drain, not capable) and state decision making. Using CMS expenditure data and survey data from the Disability Attitudes - Implicit Association Test, authors found a negative association between state prejudice scores and state funding of home health and community-based services. While causality cannot be assumed, authors conclude by stressing the importance of understanding how disability prejudice is embedded into our society, and how it may influence Medicaid and other policy decisions. These findings are a call to advocate for increased investment in community services and to promote advocacy for the health and well-being of people with disabilities.

Author(s): Emmalise Earl, Seton Hall University, Judicial Law Clerk in New Jersey Court System

Article Type: Peer-reviewed journal

This article discusses long-standing systemic issues with having accessible health care tools and equipment for people with physical disabilities. Despite the passage of the American Disabilities Act in 1973, which requires hospitals and clinics to have physically accessible equipment for care for all individuals regardless of mobility status, the Act has gone loosely enforced for decades according to the author. Lack of accessible equipment for routine checkups, such as scales and exam tables, results in incomplete examinations, later and more severe diagnoses due to inability to screen those with mobility related disabilities, as well as an exacerbation of current diagnoses due to incomplete or less effective treatment. The author states that “without more aggressive enforcement, these circumstances are not likely to change”. The author uses the Department of Veterans Affairs (VA) hospitals as an exemplar for what is needed to uphold accessibility standards. The VA requires all new medical equipment to be approved as accessible by their Access Board. The author also describes specific program actions that the Center for Medicare and Medicaid Services needs to take in enforcing equitable access to medical equipment. For Medicaid in particular, the author suggests that state Medicaid agencies adopt and enforce standards that facilities and providers must follow in order to participate in the Medicaid program. The authors also suggest leveraging tax incentives to overcome financial barriers to accessibility.

Author(s): Rupa S. Valdez, the Departments of Public Health Sciences and Engineering Systems and Environment, University of Virginia; and Bonnielin Swenor, the Disability Health Research Center, Bloomberg School of Public Health, Johns Hopkins University

Article Type: Peer-reviewed journal perspective

This article discusses the details of systemic ableism and its effects on those with intellectual and/or physical disabilities. The authors maintain that this underlying factor of health inequities is often ignored in health care and research spaces. In addition, more attention is needed on the ways structural ableism interacts with other forms of oppression. The core purpose of this article is to highlight achievable and actionable solutions for alleviating bias and discrimination of those with disabilities. Proposed solutions include establishing measures of structural ableism within research and providing accessibility options within physical environments (e.g.  streets & roadways, buildings, neighborhoods, and cities). The authors also emphasize a need for the adaptation of measures of structural racism plus the addition of new measurement domains. Of particular importance for the authors is measuring both the funding allocated for home and community based services within the Medicaid program as well as measuring the rate of violations of the Olmstead decision, which entitles those with disabilities to community integration and community-based services. Consideration of qualitative methods and community partnership in this work is also crucial for creating actionable and effective solutions to issues of systemic ableism.

Author(s): Ruqaiijah Yearby, Professor of Law at Ohio State University

Article Type: Peer-reviewed journal

This article discusses the historical context and implications of Medicaid’s origins. For example, Title VI of the Civil Rights Act of 1964 was designed to support hospital-level integration but did not apply to individual-level providers, which allowed for racism to persist especially directed toward Black people. The racist conduct of providers persisted beyond Title VI, creating mistrust and deterring Black people from seeking health care even today. Yearby connects key aspects of systemic racism to health inequity, such as housing discrimination, the wealth gap, and employment discrimination. She goes on to discuss ways in which these issues are not permanent – that they can be resolved through multifaceted solutions aimed at holding institutions accountable for racial disparities in their health care, such as further diversity training for health care staff at all levels, emphasis on cultural humility over cultural competency, and, on the federal level, implementation of new anti-discrimination laws that hold institutions (such as health care systems) accountable for vast or increasing disparities among their patients.

*Another article of interest by Ruqaiijah Yearby: Yearby R. and Mohapatra S. (2021). Systemic Racism, The Government’s Pandemic Response, and Racial Inequities in COVID-19. Emory Law Journal, 70(7), 1418–1473.

Author(s): Sanders Korenman, Dahlia Remler, City University of New York Graduate Center; Rosemary Hyson, City University of New York, Baruch College

Article Type: Peer-reviewed journal

Authors explain how a newly constructed measure of poverty, called the “Health-Inclusive Poverty Measure,” that accounts for both health insurance needs and resources to meet them, builds on the research related to the impact of Medicaid expansion on poverty. The premise for this new measure is that health insurance is a basic necessity and should be incorporated into how poverty is measured. The Census Bureau’s supplemental poverty measure, another common measure of poverty, accounts for indirect effects of health insurance on poverty. Comparatively, the new Health Inclusive Poverty Measure adds insurance needs, does not deduct out-of-pocket spending on premiums, adds health insurance benefits, and caps other deductions, such as deductibles and copays. Using this new measure, the authors explain that Medicaid can move a family out of poverty when their resources are above the measure threshold or keep them from falling into poverty due to out-of-pocket expenses. Authors conduct logistical regressions and show that the poverty rate as defined by the new health-inclusive measure is lower in expansion states than non-expansion states; the deep poverty rate is lower, too, in expansion states versus non-expansion states. Differences were generally smaller and not statistically significant when using the supplemental measure. Thus, the authors conclude that any rollbacks in Medicaid expansion would not only hurt public health, but also increase poverty as well.

Author(s): Lonni Snowden, Health Policy and Management, University of California Berkeley; and Genevieve Graaf, School of Social Work, University of Texas at Arlington

Article Type: Peer-reviewed journal

This article elevates the structural determinants of African American individuals’ physical and psychological well-being, namely stereotypes and biases that deny these individuals much-needed health insurance coverage and treatment. Authors attribute greater African American-White disparity in coverage to African American individuals’ disproportionate residence in states that declined to expand Medicaid. Authors build on earlier research by Colleen Grogan and Sung-geun Ethan Park documenting the association between state’s acceptance of Medicaid expansion and representation of African American people and White peoples’ willingness to accept expansion.* In addition, while stigma associated with Medicaid coverage has lessened for some population groups, it has not for the “non-deserving” poor, i.e., nonelderly, nondisabled adults. In fact, studies suggest that negative attitudes towards Black people explains opposition to welfare spending and public health insurance coverage. Authors call on additional research documenting both the benefits of expansion and how biases act as a barrier. The authors also encourage Medicaid administrators and providers to offer culturally sensitive care.

*Grogan, C. M., & Park, S. (Ethan). (2017). The Racial Divide in State Medicaid Expansions. Journal of Health Politics, Policy and Law, 42(3), 539–572. https://doi.org/10.1215/03616878-3802977

Author(s): Brian McGregor, Glenda Wrenn and Kisha Holden, Department of Psychiatry and Behavioral Sciences & The Satcher Health Leadership Institute, Morehouse School of Medicine, Atlanta, Georgia; Chaohua Li and Peter Baltrus, National Center for Primary Care

Article Type: Peer-reviewed journal

This article explores disparities in uptake and modality of treatment for depression for those who are enrolled in Medicaid and seeking mental health care. Authors analyze data from a nationally representative sample of Medicaid claims (in 28 states and the District of Columbia) from 2008-2009. The study identified that African American Medicaid enrollees diagnosed with depression were about half as likely to have received treatment compared to white Medicaid enrollees diagnosed with depression; Hispanic Medicaid enrollees diagnosed with depression were about three-quarters as likely to have received treatment compared to white Medicaid enrollees diagnosed with depression. Additionally, African Americans who received treatment for their depression were “…less likely to receive medication alone…”, but more likely to only be in therapy (without medication) compared to whites. These findings stood when controlled for medical comorbidities, neighborhood income inequality and poverty, and neighborhood educational context. The authors attribute these disparities partially to cultural differences and stigma of receiving mental health care, as well as provider implicit and explicit bias and structural factors that perpetuate inequities. The authors recommend integrated care models as a way to overcome stigma and improve mental health care access.

Author(s): Elisa Minoff, Senior Policy Analyst at Center for the Study of Social Policy

Article Type: Report

This resource, written by a policy analyst in an advocacy organization, provides a detailed history of work requirements in the U.S. and how these policies are based on a bias that certain people, i.e., Black people, do not want to work. This report also argues that these policies were written to coerce people, primarily Black people, into certain forms of labor thus inflating the standing of White people and putting any assistance available to non-White people at risk. Despite a lack of evidence in favor of these policies for the well-being of all, they continue to be promoted. For example, the Medicaid work requirements under the Trump Administration proved harmful to families; evaluation of the policy in Arkansas’ showed that the Medicaid work requirement led to coverage losses and no employment gains).* The author argues that in order to stop the creation of policies rooted in structural racism, it is important to understand “how we got here.” Beginning with slavery and White enslavers perpetuating racist stereotypes about Black people, the author discusses how this has evolved to public assistance policies requiring primarily Black families to work in low-wage, insecure jobs. “Work requirements not only deny families much-needed assistance, but they also discount much of their labor, ignoring the caregiving work that people provide to their loved ones….” The author advocates for the abolishment of work requirements and the promotion of policies, e.g., higher minimum wage, child care, and paid family leave, that value all work, no matter the setting or wage.

*Sommers, B. D., Goldman, A. L., Blendon, R. J., Orav, E. J., & Epstein, A. M. (2019). Medicaid Work Requirements — Results from the First Year in Arkansas. New England Journal of Medicine, 381(11), 1073–1082. https://doi.org/10.1056/nejmsr1901772

Author(s): LaShyra T. Nolen, Founding Executive Director of We Got Us and Current Student Harvard Medical School; Adam L. Beckman, Medical Student at Harvard Medical School and Harvard Business School; Emma Sandoe, Associate Director of Strategy and Planning at North Carolina Medicaid and Adjunct Professor at Duke University

Article Type: Peer-reviewed online brief

The authors examine foundational moments in the history of the Medicaid program—the creation of Medicaid (1965), welfare reform (1996), the ACA Medicaid expansion (2012), and the COVID-19 pandemic (2020)—that led to inequities in access to care as well as the racial disparities and disparate health outcomes that resulted. The authors call for policy changes in Medicaid that focus on: improving access to care for marginalized communities; prioritizing clinical care to address diseases and conditions that have disproportionately affected Black Americans; diversifying the health care and nursing facility workforce; and incentivizing nursing facilities to provide minority patient access to care while also address disparities minority patients often face.

Author(s): Paul R. Schafer, Professor at Boston University School of Public Health; Nambi Ndugga, Policy Analyst at the Kaiser Family Foundation’s Racial Equity and Health Policy Program

Article Type: Peer-reviewed journal perspective

This American Journal of Public Health Perspective written at the height of the COVID-19 pandemic by scholars at Boston University raises concerns about some states using flexibilities offered in the Medicaid program to exacerbate inequities. The authors cite the Trump Administration initiatives restricting benefits and spending (such as converting Medicaid to a block grant, work requirements, and restrictions on retroactive eligibility) as having a disproportionate negative effect on Black Americans and people of color. The authors move on to caution decision makers against promoting rather than reversing institutional racism in initiatives like these. These initiatives, regardless of if they were established with racist intent or not, demonstrate that inequities are still built into Medicaid’s policies and practices today – and that we need to replace them with equitable policies that benefit those most in need.

Author(s): Elise Trott Jaramillo, Associate Research Scientist at the Pacific Institute for Research and Evaluation (PIRE-Southwest); Cathleen Willging, Center Director and Senior Research Scientist II at the Pacific Institute for Research and Evaluation (PIRE-Southwest)

Article Type: Peer-reviewed journal

This peer-reviewed article provides a qualitative perspective on the experiences of Native American elders in the health care system across the United States. Native American people have experienced significantly higher rates of mortality from heart disease, higher rates of diabetes and mental health concerns, and have the lowest life expectancy of any aggregated race in the country. This is attributed to the lack of sufficient funding for the Indian Health Service, a separate health system that is meant to serve enrolled members of federally recognized tribes. While the expansion of Medicaid and other provisions under the Affordable Care Act (ACA) improved access to health insurance coverage for American Indian people, concerns of inadequate services sparked this research study, which consisted of semi-structured interviews with 95 elders between June 2016 and March 2017. The study found the elders lacked confidence in three main aspects of the health care system: interactions with providers (e.g., lack of trust, accessible communication, and/or coordination); identification of health insurance coverage and health care costs (e.g., confusion); and federal policy for American Indians. The authors conclude with a call to action to address health care hesitancy in a way that does not increase the complexity that Native people already face in navigating the health care system, but instead focuses resources on systemic and provider-centric changes that can build confidence for American Indian people seeking care.

Author(s): Paula Amina Alio, Professor in the Department of Public Health Sciences at the University of Rochester; Mitchell J. Wharton, Associate Professor of Clinical Nursing and Associate Dean for Equity and Inclusion at the University of Rochester; Kevin Fiscella, Professor in the Departments of Family Medicine and Public Health Sciences at the University of Rochester

Article Type: Commentary

Authors in this commentary share their perspectives on findings from a secret shopper study building off of the established association between having Medicaid coverage and a lower likelihood of scheduling specialty care appointments compared to those with private insurance coverage. In that secret shopper study from Marks et al*, researchers found that only two thirds of facilities accepted new patient appointments for cancer treatment for patients covered by Medicaid. Authors of this commentary suggest that downstream solutions, including improved reimbursement and adoption of new payment models, are not enough to help resolve these issues of access to care. They aim to raise awareness of structural racism in health care and promote equity-centered health care policies over those that only advantage white populations. Examples of the authors’ suggested solutions include Centers for Medicaid Services (CMS) requiring facilities to make their Medicaid policies public as well as incorporating ‘access to Medicaid’ in managed care and accreditation organizations requirements and standards. Improving data collection, gathering patient experience exit surveys, and establishing patient grievance processes were also proposed as possible solutions.

*Marks, V., Hsiang, W., Nie, J., Demkowicz, P., Umer, W., Haleem, A., Galal, B., Pak, I., Kim, D., Salazar, M. C., Berger, E. R., & Leapman, M. (2022). Acceptance of Simulated Adult Patients With Medicaid Insurance Seeking Care in a Cancer Hospital for a New Cancer Diagnosis. JAMA Network Open, 5(7), e2222214–e2222214. https://doi.org/10.1001/jamanetworkopen.2022.22214

Author(s): Sarah Somers, Managing Attorney of the National Health Law Program’s (NHeLP) Chapel Hill, North Carolina Office; Jane Perkins, Legal Director of the National Health Law
Program (NHeLP)

Article Type: Peer-reviewed journal

This resource discusses the history of Medicaid and makes key observations about the paradox of the Medicaid program – that while Medicaid has decreased disparities in health insurance coverage and access among the poor and people of color, the program was also founded on inherently racist premises. The authors point to three distinct Medicaid policies that shaped its weaknesses. First, the program’s beginnings were not federal; it was an optional state-level program. This resulted in disparities between states, as the authors say, “States in the South lagged. Thirty-two states had adopted Medicaid before even the first former Confederate state had adopted it.” The second major issue with Medicaid’s foundations that authors call out was its roots in the voluntary health coverage program under the Kerr-Mills Act of 1960, which had the stigma of a welfare program. The authors point out that in order, “to qualify, a person had to be poor and fit with a population group deemed worthy of coverage.” The third major concern with Medicaid’s history according to these authors is its fundamental coverage, delegation of decision making, and enforcement of covered services to states. Despite protections afforded under Title VI of the Civil Rights Act, extremely segregated facilities and disparities in both services and outcomes exist to this day. Authors discuss ways Medicaid can address systemic racism, including encouraging the expansion of Medicaid in states that have not yet made that decision, the addition of requirements to improve health equity in state contracts with Medicaid managed care plans, and the improvement of collection and reporting of disaggregated data. 

Author(s): Jacob Wallace, Professor at Yale School of Public Health, Anthony Lollo, Professor at Yale School of Public Health, Kate Duchowny, University of California – San Francisco, Chima Ndumele, Professor at Yale School of Public Health, Matthew Lavallee, Yale University.

Article Type: Peer-reviewed journal

This article utilizes 2016 administrative records from three Southern and Midwest state Medicaid programs to compare whether there were differences in health care spending and utilization between nearly two million black and white Medicaid enrollees. Results indicated that spending on adult Black enrollees was less than adult white enrollees after adjusting for demographic characteristics and health status. Additionally, Black Medicaid adults and children utilized health care less, including primary care, but visited the emergency department more than white Medicaid populations. Regarding preventive care, Black enrollees had higher rates of measures of some screenings, e.g., breast cancer, cervical cancer, chlamydia, than white enrollees. However, Black enrollees with asthma, diabetes, and cardiovascular conditions filled fewer pharmaceutical prescriptions than white enrollees. The authors attributed these differences in part to the structural and interpersonal racism that racial and ethnic minority groups face when navigating the health care system, as well as reduced access to care despite coverage increases for racial minorities overall. The authors recommend improvements to Medicaid managed care risk adjustment practices as Black enrollees are currently undercompensated in coverage due to unmet need. In addition, authors suggest a need to align plan and provider incentives to address health equity in the Medicaid program.

Author(s): Ayan Goran, Policy Analyst at the Georgetown Center on Poverty and Inequality (GCPI); Laura Tatum, Managing Director of Policy & Research at GCPI; Cara Brumfield, Director of Income and Work Supports at the Center for Law and Social Policy (CLASP); Aileen Carr, Interim Executive Director of GCPI

Article Type: Report

This report discusses how many aspects of the Medicaid and Children’s Health Insurance Program (CHIP) programs contribute to health inequities among enrolled people of color. The report covers key historical factors, such as the low reimbursement rates to hospitals and clinics for services, continued racial segregation in nursing facilities, and limited coverage for birthing people and their newborns. The latter likely contributes to the United States’ maternal mortality rate ranking highest among developed countries. The authors also specifically emphasize systemic and administrative barriers in the enrollment process, highlighting political and media narratives that have resulted in exclusionary policies directed toward single mothers of color, particularly black women, as well as immigrants. Work requirements were another key exclusionary factor, as well as a quick turnaround on verification processes that relied on paper mail to arrive at the correct address in a timely manner among other administrative burdens. This report provides multiple recommendations on how to address these issues within both Medicaid and CHIP, including taking action at the federal level to close the coverage gap both in states that have not expanded Medicaid and for certain populations, making CHIP funding permanent, increasing Medicaid reimbursement rates, and alleviating administrative burdens. Additionally, authors point to centering community voices and empowering program participants through partnerships with community advocacy organizations and community health workers, compensating these organizations and/or individuals for their time.

Author(s): Simon Haeder, Department of Health Policy & Management, Texas A & M University; Donald Moynihan, School of Public Policy, Georgetown University

Article Type: Peer-reviewed journal

This piece uses survey data to explore the relationship between racial resentment and public attitudes towards administrative policies in public programs such as Medicaid and the Supplemental Nutrition Assistance Program (SNAP). A random sample of adults with either Medicaid or SNAP were surveyed about the effects of administrative burdens (i.e., requiring in person interviews, lack of presumptive eligibility, lack of express lane eligibility, more frequent renewals, work requirements, and lack of continuous coverage) on program enrollment; a treatment group received additional information on how administrative burdens affect certain populations or exacerbate racial inequities in the survey introduction, while a control group did not receive this additional information. Authors found no relationship between exposure to this information and support for state actions associated with each of the six types of administrative burden. However, authors did find a relationship between support for administratively burdensome policies and racial resentment. Based on an analysis of non-Hispanic white respondents who were asked about racial resentment toward Black people, those with higher levels of racial resentment were more supportive of Medicaid-specific policies that would create burden. Implications for policy makers, according to the authors, include that the general public’s views on how state actions affect different socioeconomic groups are very important to the legislative process, and these views have an impact on support for new or proposed policies. However, it is also important to note that the finding that the public is hesitant to reduce initial enrollment burdens (such as work requirements) may be due to concerns of program integrity and combating fraud in addition to racial resentment. Overall, the public is more supportive of policies that reduce burden after enrollment, such as less frequent renewals and elimination of in-person interview requirements.

Author(s): Leighton Ku, Professor and Director of the Center for Health Policy Research at the Milken Institute School of Public Health, George Washington University

Article Type: Perspective in peer-reviewed journal

The author provides the historical context for programs like Medicaid and SNAP, explaining how they fill a gap in services for individuals and households living in poverty and addressing disparities in access to health care and food. While progress has been made, these programs are currently operating in an environment that runs counter to their original goals. While not explicitly racist, certain administrative policies (such as work requirements and immigration status restrictions), can be implicitly so, as they often have a disproportionately negative effect on specific populations of color. The author recommends that agencies administering these programs should reconsider policies that hinder enrollment and benefits.

Author(s): Jamila Michener, Professor of Government and Public Policy, Co-Director of the Center of Health Equity at Cornell University*;  Tiffany N. Ford, Brookings Institution at University of Illinois at Chicago

Article Type: Peer-reviewed journal

This article discusses the important context of racism and three core principles that the authors see as key to understanding and implementing policy changes related to health and racial equity. Those three core principles are described as: “interlocking systems of oppression”, “cumulative disadvantage”, and “power”. Racism operates both alongside and interlocked with other systems of oppression, such as patriarchy, structural sexism, ageism, sizeism, ableism, homophobia, and others, which have impacted society both historically and in the present day by shaping the ways in which people live. Racist and oppressive policies can have a cumulative negative effect (“cumulative disadvantage”) across systems (examples of such systems include “child welfare, public assistance, banking, incarceration, employment, housing”), and generally throughout one’s life course. The authors state that studying and addressing policies in these areas in isolation is not productive – “people and communities experience these policy arenas as overlapping aspects of daily life” just as they experience many “interlocking systems of oppression” at once. The authors also discuss the complex relationship between the concepts of power and race, arguing that power fuels racism. Race, the authors say, is not a biological fact, but rather a social construct based on appearances. And power, according to the authors, is based on where a group falls on a socially constructed racial hierarchy. Thus, power fuels racism, as groups in power will act to both construct and maintain systems that perpetuate inequities and keep themselves at the top of the hierarchy. The Medicaid program is discussed by the authors as having many policies that perpetuate these differences between races and create both cumulative disadvantage and power imbalances, with work requirements used as a prime example. The authors suggest that progress towards a more equitable future for everyone requires program design, policymaking, data collection, and research that both collaborates with and centers communities experiencing inequities. The authors also propose engaging professionals in various disciplines, such as public health, public policy, and urban planning, as well as different sectors of organizations such as academia, government, and non-profits, in the creation and revision of equitable policies and programs.

*Other resources from Jamila Michener include her book, Fragmented Democracy: Medicaid, Federalism, and Unequal Politics, as well as this Vox article on the politics and policy of racism in American health care.