1 of 4

What is William's Syndrome?

William's Syndrome is a rare genetic condition caused by the deletion of genes on chromosome 7, affecting about 1 in 7,500 to 10,000 people. It is characterized by unique facial features, cardiovascular issues like supravalvular aortic stenosis, developmental delays, and a highly social, friendly personality.

Learn More!

CANDLE OF THE MONTH:

COME TRY OUR NEW SEASONAL SCENTS!

Shop Now