Ostomy Canada Society
By Mr Colitis Stoma, Harvey Gladwell Hello, my name is Harvey, aka mr colitis stoma on social media. I’m 22 years old and am from the
By Katherine Huitema In October of 2021, at the age of 25, I was diagnosed with ulcerative colitis (UC). I had no idea what it was.
A mother shares her daughter’s journey living with OEIS syndrome, an imperforate anus, and an ostomy. This heartfelt story explores resilience, caregiving, medical challenges, and the quiet strength families discover while navigating life with complex health conditions.
Holly shares the moving story of her son Easton, who was born with an imperforate anus and lives with an ostomy, and how a classroom presentation helped his peers better understand his body and medical experiences. This heartfelt blog explores disability representation, inclusion, and the importance of open conversations that help children with medical differences feel seen, accepted, and less alone.
Sean Currie shares his journey with Crohn’s disease, surgery, and life with an ileostomy—alongside his role as a photographer for Ostomy Canada Youth Camp and Calgary Ostomy, and finding freedom beyond illness.
By Karen Bruton RN BScN MCISc-WH WOCC(C). Originally published in the Fall 2024 issue of Ostomy Canada Magazine. One of the most common ostomy complications
A cancer survivor with two ostomy bags cycles 1,160 km across Thailand, proving that life after cancer and stoma surgery can still be bold, active, and inspiring.
A powerful reflection on life with a colostomy—how irrigation, vulnerability, and community support can lead to freedom, healing, and self-acceptance.
After surviving childhood ulcerative colitis, cult influence, multiple bowel surgeries, and profound family trauma, Tiffany Shorson shares how therapy, community, and ostomy support helped her reclaim her life. A powerful story of resilience, healing, and the life-changing importance of support.
