Advocacy Committee Meeting
The National MPS Society’s Monthly Advocacy Group is a welcoming space for individuals and families impacted by MPS and related diseases who want to stay informed, share their voices, and help drive meaningful change.
The National MPS Society’s Monthly Advocacy Group is a welcoming space for individuals and families impacted by MPS and related diseases who want to stay informed, share their voices, and help drive meaningful change.
This four-part webinar series is designed to support individuals and families in the rare disease community as they explore the power of storytelling as a tool for connection, impact, and change.
Hola MPS is a welcoming space focused on supporting and connecting individuals and families impacted by MPS and ML, while strengthening Spanish-language resources and culturally relevant support across our community. […]
This four-part webinar series is designed to support individuals and families in the rare disease community as they explore the power of storytelling as a tool for connection, impact, and change.
This four-part webinar series is designed to support individuals and families in the rare disease community as they explore the power of storytelling as a tool for connection, impact, and change.
Join us for a timed 5K run & walk event, beginning at 9 AM on Saturday, March 28, 2026.
Join us for a timed 5K run & walk event, beginning at 9 AM on Sunday, April 26, 2026.
The National MPS Society invites you to attend its 40th Annual Family & Scientific Conference in Cincinnati, OH, on July 31-August 2, 2026.