Press Release
Calgary, June 1, 2023 – Crohn’s and Colitis Canada, a national health charity, today released the 2023 Impact of Inflammatory Bowel Disease in Canada report – a comprehensive snapshot of the state of care and implications for the future.
(Note: Inflammatory bowel disease (IBD) describes a group of conditions, the two main forms of which are Crohn’s disease and ulcerative colitis. These cause inflammation, ulcers and bleeding in the bowel that can extend to the rest of the body. IBD is a completely different disease from irritable bowel syndrome (IBS), which does not result in visible inflammation or ulcers in the bowel.)
The report includes findings that need to be addressed to improve the lives of those impacted with these diseases:
The number of people in Canada with IBD is increasing rapidly:
Dr. Eric Benchimol, report co-chair, and Professor of Paediatrics and Clinical Epidemiology at the University of Toronto, Senior Core Scientist at ICES, and Northbridge Chair in IBD at the Hospital for Sick Children in Toronto, says: “We see there is a significant impact on mental health – psychiatric disorders are 1.5-2 times more common in people with IBD. Youth with IBD have nearly double the risk of psychiatric diagnosis. This underlines the importance of making mental health services available, especially in children, adolescents and young adults.”
Dr. Gilaad Kaplan, a Professor of Medicine, adult, gastroenterologist, epidemiologist at the University of Calgary and report co-chair, says: “The number of people in Canada living with IBD is growing rapidly. Healthcare needs to evolve to include multidisciplinary care, including access to specialist physicians and nurses, mental health professionals, dietitians and others to improve quality of life.”
This is the fourth comprehensive report, the first was published in 2008. They bring together experts to provide a comprehensive overview of the impact of IBD in Canada. The 2023 report is available at crohnsandcolitiscanada.ca/2023report as of June 1.
Lori Radke, CEO, Crohn’s and Colitis Canada, said: “The report highlights the need to use our financial and health care resources as effectively as possible. That’s why, since 2016, our PACE network project has brought together leading Canadian hospital centres to develop best practices to help patients. We’re hoping that within the next two years, we start seeing these pilot innovations being rolled out across Canada and leading to better care.”
An innovation for this report was involving patient reviewers. One of them was Léa Caplan of Calgary. She was diagnosed with Crohn’s disease in 2020: “IBD has been an important part of my life for the last three years, so I was happy to be one of the dozens of patient partners. It’s meaningful to know that this report was prepared with individuals living with IBD and is for individuals living with IBD. Our voices are being heard.”
Watch the launch of this report—tune in to the live Zoom meeting on June 1 at 11:30 MT / 1:30 ET.
About Crohn’s and Colitis Canada
We are on a relentless journey to transform the lives of people affected by Crohn’s disease and ulcerative colitis by delivering impact at all stages of life, in every corner of the country, by
Our 2023-2026 Impact Strategy creates a roadmap for our journey with a focus on
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For more information, contact:
Paul Kilbertus
Senior Manager, Communications and PR, Crohn’s and Colitis Canada
Pkilbertus@crohnsandcolitis.ca
647-567-4690
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