The CNOC Family Advisory Council brings together patients, parents, and caregivers with lived experience in congenital heart disease and cardiac neurodevelopment. The council was created to strengthen the integration of patient and family voice across CNOC’s work, including research, education, clinical resources, outreach, advocacy, and committee-based projects.
CNOC Family Advisory Council has been holding introductory meetings with leadership from all CNOC committees about advisory integration. This has been incredibly helpful in understanding each committee’s current work, upcoming priorities, and where patient and caregiver advisory partnership may be most useful. Soon advisory members will be assigned to respective committees with the goal of representing the broader CHD community and bringing meaningful lived experiences into CNOC’s work.
Patients, caregivers, and family members who may be interested in contributing their lived experience to CNOC’s work are invited to apply to participate. More information about the Family Advisory Council, including a fun informational video can be found here https://cardiacneuro.org/for-patients-and-families/family-advisory-council-page/.