Colin Farrell has typically been very private about his home life, but now he’s opening up about his experience having a child with Angelman syndrome. Despite being relatively common, affecting 1 in ...

For the first time, Colin Farrell has opened up his home and talked in-depth about life with his son James, who has Angelman syndrome. James was just a toddler when he was diagnosed with the rare ...

Mothers are often encouraged to trust their instincts, especially regarding their children's health. But for Tiffany Young, getting others to take her concerns seriously proved challenging when her ...

Henry Edberg dug through the play kitchen at his home in Rosemount before serving up the daily special to his older brother. “Vegetables are healthy, so I’m giving you the vegetables,” Henry, 3, told ...

Angelman syndrome affects roughly 1 in every 20,000 children and it has no approved treatment. Researchers recently published results of early tests of a gene therapy strategy for Angelman syndrome, a ...

Actor Colin Farrell recently disclosed that his son, James, has Angelman syndrome, one of the driving factors behind Farrell's support for finding a cure for Angelman syndrome and for launching the ...

Actor Colin Farrell, long an advocate for people with intellectual disabilities, has started a foundation in honor of his son, James, who suffers from Angelman syndrome, a rare neurogenetic disorder.

Colin Farrell revealed that his 20-year-old son, James, has been living with a disorder known as Angelman Syndrome. While speaking with PEOPLE in a recent interview, the Saving Mr. Banks star, 48, ...

Massachusetts General Hospital in Boston announced the opening of its new Angelman Syndrome Clinic — one of only two in the country, according to the release. The clinic was established through a ...

ION582 showed robust and consistent benefit in communication, cognition and motor function in a broad patient population evaluated with a comprehensive set of assessment tools that collect input from ...

About two years ago, Midland resident Felicia Warner was sent a YouTube video from a friend that showed a child with Angelman Syndrome, a rare genetic disorder. The friend sent this video because it ...

William Edberg smiles as he takes a a bite of his favorite meal, macaroni and cheese, on Saturday, Feb. 4, 2023, in his Rosemount, Minnesota, home. Born with Angelman syndrome, a rare neurogenetic ...