In a touching and unprecedented move, acclaimed Hollywood actor Colin Farrell has shared a video featuring his son James, who lives with Angelman syndrome, a rare neurogenetic disorder. Read More
This marks the first time Farrell has publicly shared such an intimate glimpse into their life together, aiming to raise awareness and foster understanding about the challenges and joys of living with a disability.
A Father’s Love and Advocacy
Farrell, known for his roles in films such as In Bruges and The Lobster, has always been private about his family life. However, his decision to share this video stems from a deep desire to advocate for his son and others with similar conditions. “I want the world to be kind to James,” Farrell expressed. “I want the world to treat him with kindness and respect”.
James, who is 20 years old, was diagnosed with Angelman syndrome, a condition characterized by developmental delays, lack of speech, and issues with movement and balance. Despite these challenges, James’s spirit and resilience shine through, something Farrell hopes to highlight through this video
Raising Awareness and Support
The video, which shows James engaging in everyday activities and interacting with his father, aims to break down the stigma often associated with disabilities. Farrell’s openness about his son’s condition is a powerful step towards greater awareness and acceptance. “This is the first time I’ve spoken about it, and obviously the only reason I’m speaking is I can’t ask James if he wants to do this,” Farrell explained. “I have to make a call based on knowing James’s spirit and what kind of young man he is and the goodness that he has in his heart”.
The Colin Farrell Foundation
In conjunction with the video’s release, Farrell has announced the launch of the Colin Farrell Foundation, dedicated to supporting adults with intellectual disabilities through advocacy, education, and innovative programs. This initiative is particularly crucial as many support systems for individuals with disabilities diminish once they reach adulthood. “Once your child turns 21, they’re kind of on their own,” Farrell noted. “All the safeguards that are put in place, special ed classes, that all goes away”.
A Message of Hope and Inclusion
Farrell’s heartfelt message and the establishment of his foundation underscore the importance of inclusion and support for individuals with disabilities. By sharing his family’s story, Farrell hopes to inspire others to embrace kindness and understanding. “I’m proud of him every day, because I just think he’s magic,” Farrell said of his son.
The video and the foundation are testaments to Farrell’s commitment to making the world a more inclusive place for James and others like him. As Farrell continues to use his platform to advocate for those with disabilities, his efforts serve as a powerful reminder of the impact of compassion and advocacy.
https://www.youtube.com/watch?v=JDiD8Z3lWQk
