People of Color with MS in Research
Presentation by Dr. Tirisham Gyang on the barriers that people of color may experience in joining clinical trials, and why it’s important that all people have the ability…
View ResourcePeople living with MS
Voices of MS: Our Experiences as Black Men with MS
Damian Washington, Tim Carr, Erik Nelson, & Zay Bell Brown discuss the challenges of living with MS as Black men.
View Resource
Voices of MS: Our Experiences as Research Participants
Part of the MS Foundation’s 2023 Black History Month webinar series, Yolanda Hardy moderates a discussion among Veronica Daniels Lewis, Delisa French, and Dimika Cavalier…
View Resource
Participating in Clinical Trials: Your Opportunity to Make a Difference
Inaugurating our “Living with MS as a Black Person” series, this digital educational program offers insights into clinical trials and their participation…
View Resource
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…
View Resource
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…
View Resource
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 healthcare and…
View Resource
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 MS in…
View Resource
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…
View Resource
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…
View Resource
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…
View Resource
We Are ILL
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…
View Resource