Academic and healthcare conferences often default to professional expertise, leaving patients and caregivers at the margins. In this commentary led by patient and caregiver partners, we reflect on our experiences co-designing and participating in the 2024 North American Conference on Integrated Care (NACIC24). From waived registration fees and quiet rooms to shared chairing and plenary roles, we highlight tangible steps to creating inclusive conference design processes, spaces and experiences. In reflecting on the successes and areas for additional opportunities, this article provides tangible recommendations to advance patient and caregiver inclusive engagement based on our key learnings from the NACIC24.

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