The Down Syndrome Association of Delaware (DSA of DE) is a non-profit organization dedicated to supporting individuals with Down syndrome and their families. Founded in 1979, we aim to provide resources, education, and advocacy to promote inclusion and improve the quality of life for individuals with Down syndrome. Originally founded by a small group of parents of children with Down syndrome, our organization now serves over 600 individuals with Down syndrome throughout DE and surrounding states.  Our organization is one of the most robust and prominent Down syndrome organizations in the country.