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Kylie Peacock


Kylie Peacock has lived with T1D for more than 20 years and has been an advocate and a supportive voice in the community, in particular in the area of diabetes and mental health. She has joined the Research Governance Committee and will be a patient representative for the National Diabetes Repository. Kylie hopes more people living with diabetes will consider becoming a patient partner in order to ensure diverse voices and experiences are represented in diabetes research. “Being a patient partner is extremely rewarding. Not only do I have the opportunity to contribute to meaningful and impactful research, but I have the opportunity to build important relationships with other patient partners, staff, and researchers,” she says.

Associated Programs

Digital Health Solutions for Learning Health Systems

Using health data to better understand those living with diabetes and transform diabetes self-management.

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