Family perspectives on independent living for adults with cerebral palsy: barriers, support needs, and quality of life.

Introduction: Independent living is recognized as a fundamental right under Article 19 of the Convention on the Rights of Persons with Disabilities. However, for many adults with cerebral palsy (CP) exercising this right remains challenging. Many adults with CP continue to rely on family caregivers or institutional arrangements, with consequences for autonomy and quality of life. Clinical complexity and structural barriers place families in a central position in shaping adult life trajectories. This study aimed to explore family caregivers' understandings of independent living, the barriers they encounter, and the supports they identify as necessary to promote quality of life for adults with CP and their families. Methods: An interpretive qualitative study was conducted with 165 family caregivers of adults with CP across four Spanish regions (Andalusia, Aragon, Castile and Leon, and Galicia). Interviews explored meanings attributed to independent living, perceived feasibility, support needs, caregiving experiences, and well-being. Data were analyzed using inductive thematic analysis within a reflexive framework. Results: Four main themes were identified: (1) Discussion: The findings suggest that independent living for adults with CP is constrained less by individual attitudes than by structural, organizational, and relational conditions. Families play a pivotal role in sustaining autonomy, often at considerable personal cost, which may in turn limit both caregiver well-being and the autonomy of the person with CP. Strengthening rights-based, personalized, and adequately resourced support systems, together with sustained training and emotional support for families, is essential to advance independent living and inclusive community participation for adults with CP.