Chronic kidney disease has a strong impact on the health of Indigenous people and communities. Through research and engagement, Can-SOLVE CKD is working to eliminate disparities in access to diagnosis and treatment facing First Nations, Inuit, and Métis individuals.

We are committed to respectful partnerships built on an understanding of the histories and cultures of Indigenous peoples. Through the wisdom and guidance of Indigenous patient partners, Knowledge Keepers, community leaders, academics, and health care providers, we strive to ensure Indigenous knowledge and perspectives are reflected across our research projects and governance.

The Indigenous Peoples’ Engagement and Research Council (IPERC) plays a valuable role in providing governance and oversight within the Can-SOLVE CKD Network. IPERC exists to ensure Indigenous voices are heard and to guide research priorities that affect Indigenous communities and individuals with kidney disease.

To support this mission, IPERC members actively oversee the network’s research projects, as well as the development of training materials and other initiatives.

IPERC is leading a range of activities that support researchers and patient partners to become more aware of racial biases, Indigenous voices and stories, the impact of colonization on Indigenous health, and culturally safe health research practices.

IPERC meets monthly, alternating between formal business meetings and Tea and Bannock sessions—a more casual, conversational gathering that strengthens relationship-building and open dialogue. This structure reflects a balance of governance and cultural connection, and supports meaningful engagement rooted in Indigenous values.

Across the Can-SOLVE CKD Network, Indigenous leadership, partnerships, and ways of knowing are helping shape how research is designed, carried out, and shared. Explore recent stories that show this work in action.

Building relationships, shaping research: The legacy of IPERC

For a decade, the Indigenous Peoples’ Engagement and Research Council (IPERC) has helped strengthen Indigenous leadership, shape research, foster cultural safety, and build lasting relationships that continue to influence kidney health research across Canada.

Cultural safety in action: How Indigenous partnerships are shaping research

Researchers behind two Can-SOLVE CKD projects share how Indigenous patient partners, Knowledge Keepers, and communities are helping research teams rethink engagement, challenge assumptions, and build more culturally safe, meaningful approaches to kidney research.

Bringing kidney care closer to home for First Nations communities

BC Kidney Check and Helicopters Without Borders are helping reduce barriers to care by bringing kidney screening and prevention services directly into remote First Nations communities. Learn how this partnership is supporting earlier detection, relationship-building, and access to care closer to home.

Can-SOLVE CKD has adopted Land Acknowledgements to open all virtual and in-person meetings. This is done to recognize the numerous and distinct First Nations across Canada and acknowledge their traditional stewardship over the land. We have also created a four-part learning series to share teachings on the how, what, and why of acknowledging traditional territories.

A variety of other ceremonies have been included in the network’s activities, guided by IPERC members:

These Indigenous ceremonies enhance knowledge translation and Indigenous health and wellness. Importantly, these ceremonies are also training opportunities for network members to engage in Indigenous ways of doing, knowing and being.

Storytelling is a valuable method used to share patient experiences within the network, and numerous Indigenous patient partners have shared their experiences through the Storytelling for Impact module. Their stories highlight calls to action and aim to increase awareness of patient-oriented priorities.

Another methodology involves teachings from Knowledge Keepers, as part of the Learning Pathway. Can-SOLVE CKD hosted a gathering of Knowledge Keepers from diverse First Nations to share knowledge that was converted into a virtual guidebook. The Knowledge Keepers in Research guidebook encourages researchers to honour various forms of knowledge alongside Indigenous Knowledge Keepers and helps them translate those teachings into practice. Tobacco and other offerings were gifted to the Knowledge Keepers for their participation and sharing of knowledge at the gathering.

In addition, the network’s Indigenous-focused projects have developed culturally appropriate research protocols that promote better kidney health for Indigenous communities and individuals.

On June 10, 2026, Indigenous Peoples’ Engagement and Research Council (IPERC) members Cathy Woods and Tannyce Cook took part in “Indigenous Engagement in Action: Lessons from IPERC and the Kidney Check Project,” a webinar hosted by the Canadian Donation and Transplant Research Program. Cathy is co-chair of IPERC and national patient partner lead with the Kidney Check project, while Tannyce is an IPERC member and registered nurse with Kidney Check in Manitoba. The conversation explored Indigenous engagement and leadership in kidney health research, culturally safe care, relationship-building, and the importance of community connection.

For questions or more information, please contact Indigenous Initiatives Manager Jocelyn Jones at  jocelyn.jones@ubc.ca