Every year, many families in the U.S. begin the journey, and face the need for answers and support that a diagnosis of Williams syndrome sets in motion. For 40 years, the WSA has been here to help. We provide a wealth of knowledge from both experts who have studied or worked with children and adults medically or educationally, as well as from the networking of our members who have the past personal experiences to connect and share. Today, we need your help. We want to positively impact the life

Anne-Laure est la maman de Marius, qui est atteint du syndrome de Williams et Beuren. Pour neo, elle partage son quotidien rythmé par cette maladie rare. | Neo

131K views · 875 reactions | 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 | Facebook

13K views · 226 reactions | For kids with Williams syndrome ages 0-5,...