The Angelman Strong Superhero 5K & All-Abilities Fun Run takes place Saturday, May 30 at Memorial Park in Colorado Springs.

Mary Roeloffs is a Forbes breaking news reporter covering pop culture. Actor Colin Farrell is shining light on a rare genetic disorder called Angleman syndrome in a new interview offering a peek into ...

Daybue turned Neuren into a biotech heavyweight. Now investors want to know whether the company’s next wave of rare disease drugs can repeat the trick.

Dr. Joseph D'Orazio shares his experience working as a doctor and raising a child who has a rare disease, Angelman syndrome. D'Orazio explains how the experience has impacted his professional and ...

The event centers around Immy, a young Westlake girl living with Angelman Syndrome, a rare neurogenetic disorder that affects approximately 1 in 15,000 people. Characterized by developmental delays, ...

CHESHIRE, Conn. (WTNH) — The General Motors charity car show was held on Sunday in Cheshire, benefitting families with children diagnosed with Angelman Syndrome. Quinnipiac students create customized ...

CINCINNATI (WKRC) - People came together to help fight a significant health issue. Angelman Syndrome is a rare neurogenetic disorder that can have a significant impact on movement and speech. It also ...

(COLORADO SPRINGS) — When a child is born, so is a whole host of hopes and dreams. “When you hold your child for the first time, the first time you hear their cries… you play out their lives ...

MONTROSE, Mich. (WJRT) - A Mid-Michigan family is raising money to help their 6-year-old boy with a rare genetic disorder. After spending a few months looking for action figures and fun items, Kristin ...

Colin Farrell shared an update on his eldest son James, who has a genetic disorder called Angelman syndrome, in a new interview that aired Monday on "Good Morning America". Farrell said his son's ...