Supporting the William's Syndrome Foundation
Williams Syndrome is a rare genetic disorder that affects 1 out of 10,000 people, and is a genetic condition that is present at birth and can affect anyone. It is characterized by medical problems, including cardiovascular disease, developmental delays, and learning challenges. This is close to home for us as one of our kids was diagnosed at 4 months old and we always had to get creative when trying to give him supplements. mewd, not only tastes delicious and has a great consistency, but also has all the supplements to support his needs and keep him thriving.