Foundation Updates & Grants
How to Help
Who we are

About the Foundation

The Colin Farrell Foundation is committed to transforming the lives of individuals and families living with intellectual disability through education, awareness, advocacy, and innovative programs.

Colin Farrell with Stevie
Our story

Inspired by his two sons

Colin is an award -winning actor and special needs advocate. In 2003, Colin walked with the athletes in the Special Olympics World Summer Games held in Ireland, the largest sporting event of the year. He went on to be a passionate spokesperson, supporter, and advocate for the athletes and the organization.

Colin is an active member of the Angelman community and advocates for those with intellectual disabilities. Colin’s son James was born with Angelman Syndrome, a rare neuro-genetic disorder, which made Colin’s work with those living with intellectual disabilities even more personal.

Inspired by his two sons, he is excited and deeply humbled by the hope that the Colin Farrell Foundation can help those who the larger systems of governance have neglected.

Colin Farrell with Erin
Understanding

About Intellectual Disability

Intellectual Disability refers to neurodevelopmental conditions that affect cognitive functioning and skills needed for acquisition of knowledge, problem solving, and independent living. Intellectual disability manifests before the age of 21, oftentimes prior to birth.

Intellectual disability may impact learning, communication, social, and self-care skills. Most people with intellectual disability require some form of support throughout their lives.

Milestones

Our journey

  1. August 2024

    First Donation Received

    The Colin Farrell Foundation (CFF) officially launches with its first donation, marking the start of a bold mission to uplift individuals and families living with intellectual and developmental disabilities (I/DD) through education, awareness, and innovative programs.

  2. December 2024

    First Fundraiser Held

    CFF hosts its inaugural fundraiser in partnership with several organizations and supporters from the Angelman Syndrome community and beyond for our Winter Ball in Chicago, Illinois. The Winter Ball built early momentum and raised critical support to help launch CFF’s first grantmaking initiative. See more »

  3. June 2025

    Launch of First Grant Program

    On June 1st, CFF launches its first Innovation Grant—a National Call to Action supporting bold solutions to the most urgent challenges in the I/DD community. Priority will be given to programs focused on inclusive housing, integrated employment, accessibility tools, and cross-sector partnerships. Learn more »

  4. Spring 2026 Up next

    First Family Gathering

    CFF will host families here in Los Angeles for our first official Family Gathering—a heartfelt celebration of connection, community, and the shared journey of those impacted by intellectual and developmental disabilities. Check back this fall for more event details.

Leadership

Board of Directors

Select a board member to read their bio.

Accountability

Transparency

Conflict of Interest PolicyHow directors and officers disclose potential conflicts.Donor Privacy PolicyHow we protect donor information.Whistleblower PolicyHow concerns can be reported safely.
Get involved

Help bring our mission to life

Your generosity enables us to carry out our mission.

Donate nowSee our initiatives
Skip to content