These resources have been compiled by the MS Minority Research Engagement Partnership Network (MS MREPN), a collaborative, multi-stakeholder network supported by Accelerated Cure Project for MS. If you have any questions or comments, or would like to recommend a new resource to be included, please contact us at [email protected].
The authors looked at disparities in utilization of home and community based services among White and Black individuals with MS covered by Medicaid.
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We are ILL is a patient advocacy organization created to support, educate, and unite Black women with multiple sclerosis and to improve health equity for Black women living with…
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Damian Washington, Tim Carr, Erik Nelson, & Zay Bell Brown discuss the challenges of living with MS as Black men.
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This systematic review explored the incidence, prevalence, and outcomes of Indigenous persons with MS.
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This paper offers some clinical practice insights on how to improve management of minority patients with MS
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This toolkit is designed to help researchers learn more about MS in different racial and ethnic minorities, offer insights into patient concerns, and help with appropriate and…
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