Sepsis Resources

These websites contain information for clinicians, patients & their families, and researchers, including overviews of what sepsis is, how to recongize it, and what its long-term impacts can be.

Are you a sepsis survivor looking for support, or a researcher interested in involving sepsis survivors in your research? Our Patient Advisory Council can support you - learn more here. There are also online groups available for peer support. Visit the Canadian Sepsis Foundation's Facebook page to connect to other sepsis survivors.

The Pediatric Sepsis Data CoLaboratory is an international data-sharing network of healthcare workers, policy makers, researchers, and advocacy partners collaborating to address the high burden of pediatric sepsis mortality and morbidity globally. Members have access to an open-source data repository, enabling them to 1) access guidelines, tools, algorithms, and many other resources; 2) access and share data through data sharing agreements; and 3) securely store data. Learn more and register to be a member on their website.

Respectful Environments, Equity, Diversity, and Inclusion

The Action on Sepsis Research Cluster is committed to reducing inequity and increasing inclusivity within our team and our work. The following resources provide advice and guidance on supporting a working environment and conducting research that is equitable, diverse, and inclusive.

First Nations land acknowledegement

Action on Sepsis operates on the traditional, ancestral, and unceded territory of the Coast Salish peoples — xʷməθkʷəy̓əm (Musqueam), Sḵwx̱wú7mesh (Squamish), and Səl̓ílwətaʔ/Selilwitulh (Tsleil-Waututh) Nations. We invite everyone to reflect on the traditional territories and land that they currently work and live on.

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