Ostomy Canada Society
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.
Question: My baby has an ostomy and will soon be returning to my care. I’ve been told that a nurse will provide me with teaching,
Ostomy Canada’s 2025 Youth Camp celebrated its 40th anniversary with an unforgettable week of connection, courage, and community. Ten new campers joined, one inspiring graduate was honoured, and thanks to generous sponsors, every moment was made possible. Read more about this milestone year and the lasting impact of camp.
Question: Our daughter currently has a cecostomy, which has not been effective. We’ve been advised to consider a total colectomy with end ileostomy or an
Question: Hi, the supplier of my daughter’s ostomy supplies recently started charging HST after a CRA audit. They said they were told they need to
Meet our new Ostomy Ambassador, Stalen. This courageous young boy with autism and health challenges has overcome numerous obstacles with remarkable bravery and positivity following his ileostomy surgery. His heartwarming journey highlights his resilience and inspiring achievements.
Bravery Bag Covers Are Now Available and They Are Free! Bravery Bag Covers – Finding Support For Kenzie In the Summer edition of Connects, we
