Born of the belief that today’s generation can find tomorrow’s cure, the National MPS Society finds, funds, and partners with people and programs that improve the lives of those suffering from rare progressive diseases and conducts the groundbreaking research necessary to improve their odds.
The Society supports Mucopolysaccharidoses (MPS) and Mucolipidosis (ML) through funding research, supporting newly diagnosed and long-member families, and increasing public and professional awareness. For more information on MPS and ML, please visit www.mpssociety.org.
Today, the Society is a 49-year organization that serves 11 disorders and have over 2,600 members. Our Board of Directors, Team, and members run hard-working committees that bring results to our families and patients. Our fundraising efforts have brought in an impressive 21.5 million dollars for research and family support programs since the year 2000..
The advances in recent years could not have happened without the tremendous support of our Donors, Families, Friends, and Scientific Advisory Board.
