06/05/2026
This week, a social media post involving a prenatal diagnosis of Down syndrome gained significant attention online. Since then, members of our community have reached out with questions and concerns. We believe every family deserves access to accurate, balanced, and up-to-date information when learning about Down syndrome.
Unfortunately, misinformation and outdated perceptions about Down syndrome continue to circulate. Today's individuals with Down syndrome are living longer, healthier, and more included lives than ever before. They attend school, build friendships, participate in their communities, pursue employment, and contribute their unique talents in meaningful ways.
At the Down Syndrome Association of Middle Tennessee, our mission is:
"To ensure individuals with Down syndrome are valued for their extraordinary gifts and contributions, empowering them to pursue meaningful, included lives."
Whether you are a parent, family member, healthcare professional, educator, or community member seeking information about Down syndrome, we encourage you to explore current, research-based resources. Advances in healthcare, education, inclusion, employment, and quality of life continue to expand our understanding of Down syndrome. Access to accurate, up-to-date information helps families develop a more complete understanding of the opportunities and possibilities available today.
DSAMT strives to be a trusted source of current, evidence-based information, local resources, and family support for individuals with Down syndrome and those who love them. These resources can be found on our website at www.somethingextra.org.
Thank you for helping us create a community where individuals with Down syndrome are seen, valued, included, and celebrated.