More than Child’s Play

Episode 8: One of the Lucky Few - a conversation about Down Syndrome with Megan Dodd, advocate, co-founder of the Down Syndrome and Cancer Coalition, and parent

March 7, 2019

In one of our most personal and helpful conversations yet, we are joined by Megan Dodd. Megan, a seasoned educator, reading specialist, and administrator took on a new role as Mom when her amazing son Alex entered the world. Megan takes us on an intimate, honest, and real conversation about parenting a child who happens to have Down Syndrome.  She shares her story of learning of Alex's diagnosis, struggles of finding early connections to other parents with similar experiences, tales of medical diagnoses, hospitalizations, procedures, and therapy along with triumphs and many victories for her bright and beautiful son. In her unique position as an administrator and a parent, Megan shares advice on advocating for inclusion and navigating the public school system. Through Alex's experience with a co-diagnoses of leukemia, Megan has learned and shares valuable lessons that can help every listener. She has turned her pain into power by co-founding the Down Syndrome Cancer Coalition and is an advocate and administrator of the Down Syndrome Diagnosis Network (The Rockin' Moms). In our part of the world and for many across the globe, Megan has become a "go-to mom" for those first learning about their child's diagnosis with Down Syndrome and/or Leukemia. Parents and family members of children with and without these diagnoses, therapists, and educators can all learn something to make the world a better and more inclusive place to be from listening to Megan share her story.