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Colin Farrell Details Son James Battle With Rare Neurogenetic Disorder E Online

Colin Farrell Establishes Foundation in Honor of Son with Angelman Syndrome

Farrell Shares Emotional Insight into Son's Condition

Foundation Aims to Support Families with Children with Special Needs

In a rare and emotional interview, actor Colin Farrell has revealed that he has established the Colin Farrell Foundation in honor of his 20-year-old son, James, who has Angelman syndrome.

Angelman syndrome is a rare neuro-genetic disorder that causes delayed development, intellectual disability, and speech impairment. It is often characterized by a happy and outgoing demeanor.

Farrell shared that he started the foundation to give back to families like his, who face unique challenges in caring for children with special needs.

"I hope that by sharing our story and our experience, we can help other families feel less alone," Farrell said. "We want to support them in any way we can, whether it's through financial assistance, resources, or simply a listening ear."

Farrell's foundation will provide a range of services to families, including respite care, educational programs, and financial assistance for medical expenses.


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