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Clarifying the Confusing World of Clinical Trials in Underserved Populations
This webinar, serving as the second part of MSAA’s Health Disparities in the MS Community series, aims to clarify misunderstandings regarding clinical trials within underserved…
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MS Research Mythbusting
Minority communities may experience a disproportionate burden due to MS, including a heightened risk of severe disease and disability. However, minority populations are significantly underrepresented…
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Minority Engagement in MS Research: Patient Recruitment Toolkit for Healthcare Professionals
This toolkit is designed to help healthcare providers learn more about current MS research opportunities, talk to their MS patients about them, and offer insights…
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Alliance for Research in Hispanic Multiple Sclerosis (ARHMS) Registry
The ARHMS Registry is looking to better understand unique characteristics of MS in the Hispanic population and the need for more accessible and culturally relevant…
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National African Americans with MS (NAAMS) Registry
The NAAMS Registry is a research study established with the goal of accurately estimating the number and geographic distribution of African American people diagnosed with…
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MSAA Hispanic/Latinx Advisory Board
This advisory board was founded by the Multiple Sclerosis Association of America (MSAA) with the purpose of recognizing unaddressed obstacles encountered by the Latinx MS…
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MSAA African American Advisory Board
This advisory board was founded by the Multiple Sclerosis Association of America (MSAA) with the purpose of recognizing the unaddressed difficulties encountered by the African…
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Clinical Characteristics of Multiple Sclerosis in African-Americans
This review looks at risk factor exposure, disease course, biomarkers, socioeconomic status and access to healthcare between White and Black patients with MS. It also…
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How MS Affects the Black Community
Integrated set of resources and information about prevalence, current research, research opportunities, finding community, and engagement opportunities for Black people affected by MS. Includes information…
Minority Health and Research Resources
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. If you have any questions or comments, or would like to recommend a new resource to be included, please contact us at msminorityresearch@acceleratedcure.org
Spot our logo in the upper right for resources that were produced internally.