Born of the belief 43 years ago that today's generation can find tomorrow's cure, the National MPS Society FINDS, FUNDS and PARTNERS with people and programs that are improving the lives of those suffering from rare progressive diseases and conducting the groundbreaking research necessary to improve their odds.
Today the National MPS Society is an organization that serves 12 syndrome types nationwide and have over 1100 members. Our Board of Directors, staff, and members make up five hard-working committees that bring results to our families and patients. Our fundraising efforts have brought in an impressive 12 million dollars for research and family support programs since the year 2000. To learn more about the National MPS Society, please visit our website.
The advances in recent years could not have happened without the tremendous support of our Donors, our families and friends and Scientific Advisory Board.
