October Message from Executive Director Sarah Schaefer
At the WSA, we are committed to providing support and resources to as many people with Williams syndrome and their families as possible, regardless of their circumstances. No matter where our members live, their economic status, cultural background, what they look like, sound like, act like… happy or sad, spicy or sweet–we are here for them. We also want to make sure that everyone we support sees themselves in the stories we share.