We consistently engage in outreach to both medical professionals and patient advocacy groups through publications and public policy education. Some of the ways in which we offer support and education include:

  • Publishing updates about Down Syndrome Information Act state laws and state fact sheets. We regularly update this information to keep providers and patients informed.
  • Publishing in professional journals and popular media about prenatal testing and the importance of accurate, up-to-date, and balanced of patient education and support.
  • Offering presentations at local, national and international conferences about prenatal testing, delivering a diagnosis, patient education resources, and prenatal education policies at medical, genetics, and disability advocacy conferences .