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 the 2019 Annual Fund and supporting our mission to keep the Society strong. Please read about his journey here.
The 2019 Annual Fund supports critical family support programs, ensures the successful delivery of our research program and helps advocate to Congress for key rare disease legislation. Your donation MAKES A DIFFERENCE! We can’t do it without your help. Please give to the Annual Fund now, online or by check to the National MPS Society.
