Care is not control: what does truly integrated, community-based care look like, grounded in lived experience?
Veronica Cho, Grace Gatera, Sonia Korra, Oliver A. Hugemark, Matthew Jackman, Rufaro Mushonga, Angelique Thomas, Lucero Andaluz Llerena, Bijayalaxmi Biswal, Hassan Hannan Legend, Sania Saeed, Chiamo Seraphine Njuontsop, Mithi Winona LacabaPurpose
What does it feel like when care truly works? Drawing on collective lived experience across diverse regions, systems and social contexts, this paper argues that effective care cannot be achieved through isolated clinical interventions alone. While care may exist in policy and evidence-based models, it often fails in practice when it remains disconnected from the realities of people’s everyday lives. The authors contend that meaningful care emerges from integrated, community-based approaches that recognize individuals as whole human beings shaped by culture, social conditions, histories of trauma and structural inequities.
Design/methodology/approach
This is a conceptual paper.
Findings
While care may exist in policy and evidence-based models, it often fails in practice when it remains disconnected from the realities of people’s everyday lives. The authors contend that meaningful care emerges from integrated, community-based approaches that recognize individuals as whole human beings shaped by culture, social conditions, histories of trauma and structural inequities. Integrated care extends beyond mental health services to encompass housing, employment, education, family and community networks, addressing the social determinants of distress rather than merely its symptoms. Central to this argument is the necessity of lived experience leadership.
Research limitations/implications
Peer workers, survivor advocates and experts by experience must be integral to the design, delivery and evaluation of care, not positioned at its margins. Without this leadership, integration risks reproducing entrenched hierarchies and exclusions. The paper situates this call within global rights-based commitments, including the WHO Comprehensive Mental Health Action Plan 2013–2030, the Sustainable Development Goals and the UN Convention on the Rights of Persons with Disabilities. Rather than proposing a technical model, the paper offers an attainable reorientation of care: from control to reciprocity, fragmentation to continuity and institutional confinement to community belonging and well-being.
Originality/value
Drawing on collective lived experience across diverse regions, systems and social contexts.