Did you know Williams Syndrome is a rare genetic condition that affects 1 in 10,000 people worldwide, yet remains widely unknown? Are you following along with us as we continue to share & highlight our community to help bring awareness? 💙 (Credit:teambluelobster ) | Williams Syndrome Association

For kids with Williams syndrome ages 0-5, the early years are crucial for intervention and support. At the WSA, we’re here to help families every step of the way: 🧸 Providing information on early intervention programs that use play to address developmental delays through physical, occupational, speech and music therapy. 📋 Guiding families through the process of creating an Individualized Education Program (IEP) - the roadmap for your child’s public education. 👩‍🏫 Sharing strategies that work

No one size fits all when it comes to Williams Syndrome! Autumn and her dad, WSA Board President, William Palmer share their Sunday with us! Every person with Williams Syndrome brings their own stories, strengths, and individuality. ❤️ #williamssyndrome #williamssyndromeawareness #dualdiagnosis | Williams Syndrome Association

This week our blog was about the effects of convention, and we're continuing the thread (see link for blog in comments). Mom Jennifer Ryan sent her stories/observations--feel free to share yours if you were at #SetSail2018! And enjoy a few more pictures! 1. "We take turns with childcare during the convention. While Granny (Cathy Minnella) was at a session, I took Elise (8, and dually diagnosed with Williams syndrome) to the Hard Rock Café. The adults arrived (The Dream Team--ages 38+). My daught