The Patient Partner Advisory Council (PPAC) is a group of patients and caregivers who ensure lived experience remains central to PHA Canada’s work. The Council provides advice and insight on organizational priorities, programs, advocacy efforts, and research initiatives, helping to ensure that the needs of the pulmonary hypertension (PH) community guide decision-making across the organization.

Members:

Angèle Belliveau, PAH patient, New Brunswick

Brooke Paulin, PAH patient, Ontario

Don Downey, Caregiver with lived experience, Alberta