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

Our friends with Williams syndrome aged 6-12 have been meeting virtually with special camp and convention volunteers, and recently had a dance party! They were asked to make signs ahead of time showcasing all the things they can do (many things!) and shared them. Don't miss this celebration and spirit of "Try Anything"! To learn more or sign up for these virtual gatherings (there is one for teens this Sunday): https://williams-syndrome.org/programs/virtual-programs #williamssyndrome | Williams S

Caregivers of individuals with Williams syndrome play a very important role in their journey and often serve as their greatest advocate! Andrea Johnson, a genetic counseling graduate student at the University of South Carolina, wants to learn more about the transition into adulthood for those with WS. If you are a caregiver of someone 18 with Williams syndrome, please share your experience in this survey. https://pulse.ly/sskrgq5mz7 The survey closes on Oct. 15. | Williams Syndrome Association

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

Callie Truelove is diagnosed with Williams syndrome, a rare genetic condition known to cause a joyful demanor. She loves everybody and even sees hearts in common objects all around her. Callie's parents consider her positivity a blessing, but also try to teach her not everbody can be trusted. | Special Books by Special Kids

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