The Cerebral Palsy Association of British Columbia (CPABC) is a registered non-profit organization founded in 1954 by a group of parents seeking to create better futures for their children. Today, it provides programs, support, and advocacy for people with cerebral palsy and other physical disabilities across the province.
Vision and mission
CPABC envisions a world where individuals with cerebral palsy live a “Life Without Limits.” Its mission is to raise awareness, promote inclusion, and support individuals with cerebral palsy in achieving independence, self-determination, and full community participation.
Core programs and services
Recreation and wellness
CPABC offers adapted yoga, dance, movement therapy, and inclusive social groups that promote both physical and emotional well-being.
Family and individual supports
Services include family and youth support workers, peer mentoring, caregiver connections, and guidance through transitions in education, employment, and independent living.
Public education and outreach
The organization provides disability-awareness presentations to schools, businesses, and community groups, helping to challenge stigma and improve accessibility. It also maintains a lending library of accessible resources.
Financial support
CPABC offers bursaries for post-secondary education, camperships for inclusive summer programs, and limited financial assistance for adaptive equipment and supplies.
Governance and structure
CPABC is governed by a volunteer board of directors and staffed by a small, dedicated team. It works closely with individuals with lived experience and operates with the support of donors, sponsors, and community partnerships.
Impact and reach
Serving over 1,000 individuals and families across British Columbia, CPABC delivers province-wide programming in person and online. It plays a key role in public education, early intervention, and lifelong support for people with cerebral palsy and related disabilities.
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