DOUBLE your donation for research! All donations up to $30K will be matched dollar for dollar for our June 13th virtual event.
Each year we remember individuals with MPS and ML who have passed away but who remain in our thoughts and hearts. We invite you to join us in reading about and remembering our cherished friends and family.
We are dedicated to providing our members with the latest information and support around COVID-19. We are pleased to offer the following resources to our membership and will continue to update these regularly as the situation necessitates. Coronavirus General Information Severe COVID-19 Complications and MPS and ML Patients Clinical Trial Updates During COVID-19 Infusion Considerations … Continued
Help us Raise $45,000 for International MPS Awareness Day! Join the National MPS Society as we approach International MPS Awareness Day – May 15, 2020. This year, as we celebrate 45 years of serving families, we hope to raise $45,000 in 45 days for our Family Support programs. These programs provide access to critical resources … Continued
Thank you for your interest in the MPS/ML Support Sessions. This page will be maintained to provide details for active and upcoming Zoom webinar sessions. All sessions are free and open to members of the National MPS Society and to individuals and families with MPS and ML internationally. To sign up to receive regular emails … Continued
We have events on each coast and in between to raise money to support families diagnosed with MPS and ML, please join us at a few!
The National MPS Society hosts an Annual General Membership meeting to provide updates and report back to our membership. We are here to support you! This took place via webinar on Tuesday, November 19, 2019. Click the link below to review the webinar and learn about the work of the Society over the past year.
The 2019 Annual Fund is underway! Meet Jason Madison, Chair of the 2019 Annual Fund. Jason was diagnosed with MPS II (Hunter Syndrome) at the age of six after his mother watched his uncle suffer similar symptoms. Jason Madison and the National MPS Society hope that your family will make a difference by giving to … Continued
Our annual report outlines key fundraising efforts and work of the committees over the past year. Within the annual report are details of the grants awarded and financial statements. The National MPS Society provides funding for research, support to families, and works to advocate for cures for MPS and ML. Click here to read the … Continued
Families across the country received purple birds to help raise awareness! These birds traveled around the world to spread the word about MPS. Families and individuals with MPS submitted pictures of the adventures of their purple birds. These were shared on Facebook and voted on to determine the winner of the contest for this year! … Continued