The National MPS Society exists to cure, support, and advocate for MPS and ML. Their mission serves individuals, families, and friends affected by Mucopolysaccharidoses (MPS) and Mucolipidosis (ML) through supporting research, supporting families, and increasing public and professional awareness. For more information on MPS and ML, please visit www.mpssociety.org.
Born of the belief 45 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 11 syndrome types nationwide and have over 1700 members. Our Board of Directors, staff, and members run 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.
Today the National MPS Society is an organization that serves 11 syndrome types nationwide and have over 1700 members. Our Board of Directors, staff, and members run 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.
