The Down Syndrome Association of Snohomish County is committed to creating a community where individuals with Down syndrome are valued, included, and given every opportunity to thrive. We strive to make sure families feel informed, supported, and never alone.
Below are a few of the programs we offer.
First Call
First Call is designed for parents who have just received a Down syndrome diagnosis. This can be an especially anxious time, and the first thing to understand is that you are not alone. DSASC is made up primarily of parents of children with Down syndrome, so we are in a unique position to understand and meet your needs for information and support.
The opportunity to speak with other parents who have a child or children with Down syndrome can be invaluable. If you would like to speak to a parent or caregiver in DSASC, please email info@dsasc.org
As you begin the process of learning more about Down syndrome, we ask you to be mindful of the following:
- Like every child, all children with Down syndrome are unique, with their own strengths and challenges. You can’t predict exactly what your child will be like, and you can’t base their needs or abilities on your observations of others.
- Make sure that any material you read on the topic of Down syndrome has a recent publication date. Much of the information that is available becomes outdated quickly.
- Know that the outlook for children with Down syndrome has improved tremendously in recent years due to advancements in the quality of medical care and educational support in our schools for individuals with Down syndrome.
Social Groups
Our age-based social groups create meaningful opportunities for individuals with Down syndrome to connect, build friendships, and thrive in a supportive, inclusive community. Designed for children, teens, and adults, each group offers activities tailored to developmental stages and shared interests—from play-based learning and social skill-building to community outings and peer support. These social groups allow parents of children with Down syndrome to connect with other parents facing comparable challenges, milestones, and decisions. This creates a sense of shared understanding that can be difficult to find elsewhere. Parents can exchange practical advice, celebrate progress together, and offer emotional support during setbacks, all within a context that feels relevant and timely.
Birth to 5
Kristen O’Malley is leading a Birth-5 group for our DSASC families. For more info, email Kristen at kristenomalley1@gmail.com
Ages 6-10
Needs a leader! If interested email info@dsasc.org
Ages 11-15
Needs a leader! If interested email info@dsasc.org
OLDER TEEN/YOUNG ADULT
Led by Cathy Moore and Lori Schmieder. For more information, email Lori at lori.schmieder@dsasc.org
You can also find info on our public Facebook page (DSASC) to join specific age based group.
Scholarships
Exciting things are on the way! We are currently developing a scholarship program designed to expand opportunities and provide meaningful support to children and adults with Down syndrome in our community. This initiative reflects DSASC’s commit to the goal of life long opportunities for individuals with Down syndrome. More details will be announced soon—stay tuned as we work to bring this vision to life.