(unnamed MS awareness campaign) is driven by patient voices. People living with MS have the firsthand experience of receiving a diagnosis, educating friends and family, and navigating their life as a patient with a chronic autoimmune disease. For these reasons and more, patient voices are at the center of our awareness campaign. is asked to share their valuable feedback on our existing educational tools and resources, shaping them to become more accessible for all our audiences. The Advisory Committee also guides the MS Centers outreach approach to increasing community knowledge on the early signs of MS, and committee members play an active role in shaping the trajectory of the Awareness Campaign.

By selecting to participate through our menu of options, you’re not only equipping yourself with vital information but also becoming a catalyst for change within your local community. Together, we can break down barriers and ensure that every individual, regardless of background or circumstance, can live their fullest life with MS.

Your voice matters. By sharing our social media posts, you’re amplifying our message and reaching those who may need it most. Whether you choose to share our posts or simply like and comment, every action contributes towards building a world where everyone has better access to specialized MS support services.