Crohn’s disease is a lifelong inflammatory bowel disease. Inflammation and ulceration develop in the digestive tract, most often in the lower small bowel and upper colon. Day to day that can mean cramping pain, persistent diarrhoea, tiredness and weight loss.
Crohn’s is one of two main forms of inflammatory bowel disease. Crohn’s and Colitis Canada describes it as able to strike anywhere from mouth to anus, in patches, with healthy bowel between. Ulcerative colitis differs: one continuous stretch in the colon and rectum, involving only the inner lining.
It is also not caused by anything you ate or did. The cause is not known, and Crohn’s and Colitis Canada points to genetics, environment and the gut microbiome. Food affects how you feel day to day, but it did not start the disease.
Crohn’s runs in flares and quieter stretches, and no two people are the same.

Some risk factors cannot be changed:
Others can often be worked on, usually with support from a health care team:
There is no single test. A family doctor usually starts with your history, an examination, and blood and stool tests. The Canadian Digestive Health Foundation describes the faecal calprotectin stool test as a way to see whether there is inflammation in the bowel, which helps separate inflammatory bowel disease from irritable bowel syndrome. A gastroenterologist then confirms it with endoscopy and biopsies, usually a colonoscopy reaching the end of the small bowel, plus imaging for the parts an endoscope cannot reach.
There is no cure, so care aims to settle inflammation and prevent complications. A gastroenterology team may discuss:
No two cases are alike. These are decisions for you and your own gastroenterology team.
There is no cure, and many people either never respond well to a given medicine or lose their response over time. The 2023 national report shows inflammatory bowel disease in children rising year after year while adult onset stays flat, and no one can yet explain that, or why Canadian rates are among the highest in the world. Studies are testing new biologic and small molecule targets, diet and microbiome approaches, intestinal ultrasound for monitoring, and ways to predict who will need surgery.
Taking part is voluntary. You give informed consent first, you can stop at any time without affecting your regular care, and no one can say in advance whether a study will help you personally.
This page is written in plain language for people considering clinical research. It is general health information, not medical advice, and it does not replace a conversation with your own doctor or nurse practitioner.
Both are forms of inflammatory bowel disease. Crohn's and Colitis Canada describes Crohn's as able to affect anywhere from the mouth to the anus, in patches, with healthy bowel in between, and as going deeper into the wall of the bowel. Ulcerative colitis is more localised: it affects the colon including the rectum, in one continuous stretch, and involves only the inner lining. Bleeding and urgency are more common in colitis, and mouth ulcers are more common in Crohn's. Narrowed bowel, fistulas and abscesses are complications specific to Crohn's.
No. The cause of Crohn's disease is not known. Crohn's and Colitis Canada points to a combination of genetics, environmental factors and changes in the gut microbiome. Food can affect how you feel day to day, and a dietitian can help you work out what suits you, but diet did not cause the disease. Neither did stress.
Because many people either never respond well to a given medicine or lose their response over time, and trials are how new options and better ways of using existing ones get tested. Taking part usually means extra assessments and close monitoring by a research team. Participation is voluntary, you give informed consent before anything begins, and you can withdraw at any time without affecting the care you get from your own gastroenterology team.