The Canadian PBC Society was founded in 2003 by a small group of volunteers in Toronto dedicated to improving the lives of those living with PBC. We now are a national registered charity with more than 300 members across the country with regional groups made up of patients and other concerned individuals.
- inform and educate those with PBC and their communities
- improve early diagnosis
- provide compassionate support to those suffering from PBC
- raise funds for research to help find a cure and effective treatment
We are a totally volunteer, non-profit organization managed by a small executive committee:
- Gail Wright, President
- Barbara Badstober, Past President
- Debbie Deinhart, Treasurer
- Nancy Stewart, Member Communications
- Katherine Fuerst, Advisor
We have relationships with a network of recognized world leaders in the field of PBC research who provide us with up-to-date information about the latest developments in diagnosis and treatment. They include:
- Angela Cheung, MD, FRCPC — Research Fellow, Mayo Clinic, Rochester, Minnesota.
- Andrew L. Mason MBBS, FRCPI, FAASLD — Professor of Medicine, Director, The Applied Genomic Core, Division of Gastroenterology and Hepatology, University of Alberta, Edmonton
- Mark G. Swain, MD, MSc, FRCPC, FAASLD — Professor of Medicine, Cal Wenzel Family Foundation Chair in Hepatology; Head, Division of Gastroenterology and Hepatology, University of Calgary; Head, Section of Gastroenterology and Hepatology, Alberta Health Services, Calgary Zone
The Canadian PBC Society has close links with organizations around the world, all working hard to find improved diagnosis and treatment — and ultimately to reach for a cure — for PBC.
These organizations include: