Sepsis Canada Patient Advisory Council
Within Sepsis Canada, Patient Partners include any individual(s) who have experienced sepsis themselves or are the caregiver(s) of a sepsis patient (eg. spouse, parent, child, sibling, friend, other family member).
Sepsis Canada Patient Partners help to inform the research we conduct and programs we offer by sharing their insights and lived experiences, sitting on Sepsis Canada committees (e.g., Steering Committee, Communications Committee etc.), and working alongside investigators to ensure our research is meaningful and reflects the needs of sepsis patients and their families.
The Sepsis Canada Patient Council is made up of individuals from across Canada who have lived various experiences.
Sepsis Canada has had an overwhelming response to join our Patient Advisory Council. At this time, we are no longer accepting new applications to join the council.
If you are interested in future Patient Partner opportunities, please subscribe to our newsletter.
PLEASE NOTE: Sepsis Canada is not permitted to give advice and support to sepsis survivors and their families, as our mandate is only sepsis research. If you are in need of support, please contact the Canadian Sepsis Foundation as they will be better placed to help!