NoBo is Back
Just because Matthew has limitations doesn’t mean we also stop living life. We love to travel — at least that is what my husband I and kept telling ourselves. Summer of 2017, we traveled to the Philippines, then summer of 2018, we traveled to Europe. It was fun, but very challenging and exhausting. We felt […]
Welcome to our blog
Our youngest son, Matthew, was born with a rare genetic disorder called “Angelman Syndrome.” Our family is always looking for ways to educate others on what Angelman Syndrome is as well as “special needs” in general. This summer we wanted to do something different and try to raise awareness by traveling across the United States […]