05/06/2026
At RMDSA, we believe every family deserves access to accurate, up-to-date information about Down syndrome.
Recent national conversations have highlighted why evidence-based resources and the voices of people with Down syndrome matter. Outdated stereotypes do not reflect the reality of the fulfilling, meaningful lives people with Down syndrome are living every day.
We are grateful to the Global Down Syndrome Foundation and our national partners for continuing to provide trusted information and resources for families, healthcare providers, and communities.
Learn more through this prenatal and newborn resource:
🔗 https://bit.ly/4aUSL44
People with Down syndrome are students, employees, friends, neighbors, leaders, and valued members of our communities. Accurate information matters, and so do their voices.
The Global Down Syndrome Foundation, the National Down Syndrome Congress, and the National Down Syndrome Society have teamed up to publish the third edition of the groundbreaking Prenatal & Newborn Down Syndrome Information Pamphlet, available in English, Spanish and Icelandic. The third edition