MS in the Hispanic/Latinx Community

Prevalence of Multiple Sclerosis Among Hispanic/Latinx

Symptoms of MS in Hispanics

Stories From People With MS

MS became part of Gloria Estefan’s family life after her father was diagnosed when she was a teenager. The singer reflects on how far treatments have come.

Still a Work in Progress

Crystal Bedoya’s life changed at 11 with MS symptoms. In addition to dealing with her diagnosis, she helped her Spanish-speaking parents understand her doctors.

Resources for Hispanics/Latinos Living With Multiple Sclerosis

Connect With the Hispanic/Latinx Community

The Hispanic/Latinx MS Experience Summit is an opportunity to connect with others. Listen to dynamic speakers in both Spanish and English and share your story.

Cultural Barriers to Healthcare

Race and MS

Knowledge of MS can contribute to better outcomes.

Get Involved in MS Research for the Hispanic Community

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Greater participation in research would offer a clearer picture of the impact of MS on the Hispanic/Latinx community. Investigators want to learn about the social, cultural and genetic factors that play a role in the disease. This will allow them to make changes that improve health outcomes.If you’re interested in helping determine which treatments are best and how to reduce MS risk in the community, find ongoing studies, including one that is recruiting Hispanics/Latinos with MS. Investigators are recruiting for a new study to determine whether an online program can reduce fatigue by improving self-management.For answers to questions you may have, read Participating in Clinical Trials: A Guide for People With MS.

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Mayteé, diagnosed in 2015

Your Experience Can Have an Impact

Investigators are recruiting Hispanics with an MS diagnosis for a study on genetic markers that influence disease severity. Help the Alliance for Research in Hispanic Multiple Sclerosis learn more about MS in Hispanic communities.