The Gilbert Fund

Understanding Williams Syndrome

Williams syndrome is a rare genetic disorder that affects brain structure, cognitive function, and physical health. Characterized by extreme sociability, distinct facial features, and cardiovascular issues, this condition offers a unique insight into the connection between genetics and behavior. Learn more about its causes, diagnosis, and the latest research shaping the future of Williams syndrome care.

Living With Williams Syndrome

Williams syndrome, often called the ‘Happy Syndrome,’ is a rare genetic condition that shapes both the joys and challenges of those who live with it. This article explores the social, emotional, and medical aspects of WS, highlighting the importance of support, advocacy, and inclusion for individuals and their families.