Brief History: The Massachusetts Down Syndrome Congress (MDSC), established in 1983, is an all-volunteer, non-profit organization made up of parents, professionals and anyone interested in gaining a better understanding of Down syndrome. Its roots trace back to a group of parents, in a living room in 1983, chatting about their children with Down syndrome and how they could connect and educate families, schools and communities. Twenty-two years later, with over 1,000 members, the MDSC has an energetic Board of Directors, and a vision to ensure that every person with Down syndrome has the opportunity to reach their full potential. Mission Statement To enhance on a continuous basis the lives of individuals with Down syndrome through the education and support of people with Down syndrome, their families, their friends, their teachers, and the community as a whole. To ensure individuals are valued, included, and live fulfilling lives in the community. Our Purposes · To provide new parents with information, resources, and support. · To promote the inclusion of people with Down syndrome into all aspects of the community, with particular consideration for schools and the workplace. · To gather and disseminate accurate, up-to-date information about Down syndrome. · To better educate the public about Down syndrome through the celebration of Down Syndrome Awareness Month and through an annual conference in order to advance the understanding of Down syndrome. · To encourage research related to Down syndrome and quality human services. · To address social policy issues with state and local human service agencies. · To solicit and distribute funding for these accomplishments. Our Vision The MDSC wants to be recognized by parents, educators, people with Down syndrome, and the medical community as the preeminent organization in Massachusetts for information, networking, and advocacy for and about Down syndrome.