Dr. Vito Ferro of The University of Queensland in Brisbane, Australia received a grant for his work in the field of MPS during the years of 2013-2015. We are proud … Continued
On behalf of the 15th International Symposium on MPS and Related Diseases, the Scientific Program Delegates announce the Scientific Program Oral Presenters this August 2 – 4, 2018 in San Diego, California. Selections were led … Continued
The May edition of our Courage newsletter is now available for viewing. Read it here!
The international community celebrates MPS Awareness Day each year on May 15. In an effort to spread awareness about MPS during the month of May, we’ve created this calendar with … Continued
Don’t miss this exciting opportunity to learn about new and innovative treatments, meet researchers from around the globe, and increase your network of friends and families! The symposium is … Continued
Once again, Team MPS will be participating in the Million Dollar Bike Ride on May 20th. This event, hosted by Penn Medicine Orphan Disease Center, is critical for funding research for MPS … Continued
The National MPS Society funds research that may lead to treatments for MPS and ML diseases and solicits applications for innovative research projects that involve clinical research, basic research and … Continued
Data confirm highly promising biomarker for MPS VI and limited enzyme replacement therapy (ERT) efficacy in reducing leukoGAGs Inventiva, a biopharmaceutical company developing innovative therapies in MPS, recently announced the positive … Continued
RARE Scholars, an annual scholarship for students living with rare disease, aims to empower patients with continued education by recognizing students who have demonstrated leadership and participation in school and … Continued
The latest version of Courage is now available! Click here to see the latest news and announcements from the National MPS Society.