Support for families
Research for a cure

Watch our video to see how the National MPS Society is changing lives.

Learn About MPS

Have you or your child recently been diagnosed with MPS or ML, or is your child undergoing diagnostic testing? We are here to help and can connect you with the information you need.
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Give to the National MPS Society

Donations to the National MPS Society allow us to support families affected by MPS and ML, fund medical research to find cures for these diseases and keep the public engaged and informed.
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Support those affected by MPS and ML

Families are the linchpin of our community, and whether it’s financial assistance during a hard time, a special treat for an affected family member or to help make educational dreams come true, we support MPS and ML families across the nation.
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News

Only 10 Days Left!

There’s only 10 days left to register for the Raleigh Run for Rare 5K which is raising funds to benefit ML and MPS research. The run will take place in the beautiful and historic Dorothea Dix Park in downtown Raleigh, NC. Registration opens at 7:00 a.m. and the run starts promptly at 8:00 a.m. After … Continued

The National MPS Society is proud to announce that the Research Grant Program for 2019 is officially open. In 2019 the Society will continue funding research with the goal of finding treatments and cures for MPS and ML. The application for Letters of Intent is now available for innovative research projects that involve clinical research, … Continued

#RareDiseaseDay

Our members came out strong to show support for #RareDiseaseDay and honor those that came before them and pave the way for those just starting their journey.

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Upcoming Events

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