Colin Farrell Starts Foundation in Honor of Son with Angelman Syndrome He Opens Up About Their Life.

Colin Farrell has recently launched the Colin Farrell Foundation in honor of his son, James, who has Angelman syndrome, a rare neurogenetic disorder that affects the nervous system and results in severe speech impairment and developmental delays. In a heartfelt interview, Farrell shared insights into their life together, emphasizing the need for greater support for adults with intellectual disabilities, especially as James approaches his 21st birthday, a milestone that often leads to a lack of available support systems for individuals with disabilities.
Foundation Goals
The foundation aims to provide advocacy, education, and innovative programs to assist families with members who have intellectual disabilities. Farrell expressed his desire for the world to treat James with kindness and respect, stating, "I want the world to be kind to James" and highlighting the importance of community integration for individuals like his son. He noted that once children with disabilities turn 21, many of the educational and support services they rely on disappear, leaving them vulnerable and isolated.
Personal Reflections
Farrell described James as "magic," expressing pride in his son's determination and hard work throughout his life. He shared anecdotes about James's progress, such as learning to feed himself, and emphasized the joy and fulfillment James brings to those around him.
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