I’m Suzanne. It’s been 20 years since the diagnosis of Down Syndrome became a reality for me when my son was a newborn. I’ve seen my share of challenges, but I’ve also been blessed to witness the miracles. With those first words, “your son has Down syndrome,” I also became a member of a club that I didn’t want to join, but I’ve been gifted with the most amazing people along the way. The topic I’ve grown most passionate about is full inclusion for children and people with special needs. I’m here to be a resource to you in that pursuit and hope you’ll join me in the conversation.