Patient Partners Journey with the Indigenous Peoples' Engagement & Research Council

A webinar hosted by Cathy Woods & Arlene Desjarlais, sharing about patient partners experience with the Indigenous peoples Engagement and Research Council (IPERC) with Can-SOLVE CKD. Overview of how the IPERC exists to ensure Indigenous voices are represented within research priorities that affect Indigenous peoples living chronic kidney disease.
Introducing the Indigenous Peoples Engagement and Research Council
Get to know the co-chairs and how IPERC is a governing body within the Can-SOLVE CKD Network.
Supporting the Truth and Reconciliation Call's to Action
How IPERC supports the Truth and Reconciliation Call's to Action #18, #19, #23, and #92.
How CKD affects First Nations, Métis, and Inuit peoples differently.
Current Research Projects within Can-SOLVE CKD
Research projects within Can-SOLVE CKD that aim to address kidney disease earlier.
How to be a voice within research.
For more information about CanSOLVE CKD Network, please visit: cansolveckd.ca/
For more information about IPERC and Indigenous Initiatives please visit: cansolveckd.ca...
For more information about Kidney Check, please visit: cansolveckd.ca...
For more information about Improving Indigenous patient knowledge about treatment options please visit: cansolveckd.ca...
To watch Knowledge Keepers in Research videos, please visit: cansolveckd.ca...
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