Limited representation limits research.
ACP connects researchers with communities underrepresented in research, so findings hold true for more of the people they're meant to help.
The gaps aren't random
Who participates in research is shaped by many factors — from where studies are conducted and who hears about them to eligibility criteria, participation barriers, bias, and mistrust rooted in past and present experiences. These barriers can leave some communities underrepresented and limit how well findings apply across the MS population.
More inclusive research starts here
Whether you need hands-on project support or broader tools and resources, ACP has you covered.
Consult with community advisors
The Research, Inclusion, Diversity, and Equity (RIDE) Council brings nearly 30 people living with MS from underrepresented communities to the table. Available for project consulting at every stage of your study.
Connect with a field-wide network
The MS Minority Research Engagement Partnership Network (MREPN) is a free, open network of researchers, clinicians, and community organizations working together to make MS research more representative.
The numbers behind the gap
These aren’t abstract disparities. They can shape who participates in research — and how useful the findings are for the people research is meant to serve.
> 50%
of people living with MS are 55+
1 in 5
Americans live in rural areas
93%