Diana Bozzo brings deeply personal lived experience to her role on the Board of Directors of Lupus Canada. Living with lupus has profoundly affected her life and her family, shaping a lifelong commitment to patient advocacy, public awareness, and meaningful change for the lupus community. She has played an active role in raising awareness and funds in support of lupus research and lupus clinics across the Greater Toronto Area, and helped advocate for the passing of Bill 112, an Act to proclaim Lupus Awareness Day in Ontario, a critical step in advancing visibility, education, and earlier diagnosis. At the heart of Diana’s work is an unwavering commitment to patients. She is dedicated to ensuring that the voices of those living with lupus are heard, respected, and centred in every decision and to making sure no individual or family facing this disease ever feels invisible or alone. She will ensure that patient voices are heard, valued and reflected in every conversation.