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Embodiment of structural racism and multiple sclerosis risk and outcomes in the USA
The authors review the ways in which racial and ethnic disparities in MS in the USA can be linked to bias, discrimination, and social determinants…
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Hispanic/Latinx MS Experience Program Series
Quarterly program series focused on the Hispanic/Latinx population and their unique needs. Click here to access this resource.
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Black MS Experience Program Series
Quarterly program series focused on the Black population and their unique needs. Click here to access this resource.
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Navigating Challenges and Embracing Opportunities Toward Achieving Equitable Multiple Sclerosis Care
This review explores the contemporary issues driving health disparities among people with MS including the role of race, ethnicity, and socioeconomic disadvantage, the need for…
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Race- and place-based disparities in multiple sclerosis care: A qualitative study of patient experiences
Black and White people with MS participated in focus groups and interviews aimed at understanding how race and location affect MS healthcare quality and access.…
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Race and ethnicity on MS presentation and disease course
This study explores the inequities in health along with differences in clinical characteristics observed in selected racial and ethnic populations that may be genetic, environmental,…
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Racial and ethnic disparities in treatment response and tolerability in multiple sclerosis: A comparative study
This study compares Hispanic, Black, and White patients with MS regarding disease outcome, as well as the impact of race on long-term outcomes. The findings…
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Descriptive Analysis of Health Disparities Between Black and White People With Multiple Sclerosis in the Deep South
This article reviews disparities in health outcomes as experienced by Black Persons with MS in the Deep South as compared to White Persons with MS.…
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Exploring the Landscape of MS in Black Americans
Recent research highlights a rising number of MS diagnoses among Black Americans, with many experiencing a more aggressive form of the disease. Dr. Mitzi Joi…
Research isn't finished until it reflects everyone with MS.
ACP is working to change that.