Irish star Colin Farrell has touchingly recounted his decision to place his 21 year old son into long-term care. The actor from Dublin shared his experience, explaining how his son James was initially ...

Actor Colin Farrell is launching a new foundation to raise awareness of a rare genetic condition called Angelman syndrome, so that his son and others with the disorder will have more support and ...

Add Yahoo as a preferred source to see more of our stories on Google. Back in August, Irish actor Colin Farrell won widespread praise when he emotionally opened up about the “terrifying” reality of ...

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, ...

Colin Farrell is opening up about his son’s rare neurogenetic disorder. The 48-year-old recalled the moment James was diagnosed with Angelman syndrome when he was just 2 1/2 years old. “One of the ...

Colin Farrell says his personal life has inspired him to launch a new foundation aimed at helping people with intellectual disabilities. The actor, 48, recently launched the Colin Farrell Foundation, ...

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 ...

People from across the USTA Eastern tennis community came together at the USTA Billie Jean King National Tennis Center to ...

Affected populations: The disorder is believed to affect somewhere between 1 in 12,000 and 1 in 24,000 people, although these figures may be underestimated. Many cases of Angelman syndrome can go ...

What is Angelman Syndrome? Causes, Treatments & Prognosis Learn about Angelman syndrome, a rare genetic disorder affecting the nervous system, how it is managed through therapies and medications, and ...

HAVE THEIR BAGS READY TO BE PICKED UP. NEVER IMAGINING THIS WOULD BE THEIR FATE. AN AREA FAMILY IS NOW IMMERSED IN THE RARE DISEASE COMMUNITY. KMBC9 DONNA PITMAN SHOWS US HOW THEY’VE GONE FROM A MAJOR ...