My 13 year old DGS was diagnosed with Crohn's Disease two years ago. My DS and DiL are reluctant to follow the NHS treatment route as it involves medication and a possible eventual colostomy bag. Instead, they are following a programme devised by an eminent consultant on Crohn's which should eventually provide DGS with a list of foods he can safely eat. After that, so long as he sticks to the approved foods, he should be able to live a normal life. However, this is a very slow process and DGS suffers debilitating bouts of stomach ache, wind and diarrhoea each time he tries a food that subsequently disagrees with him.
I would be interested to hear from anyone with experience of Crohn's in children as I am very worried about DGS's condition and how it may affect him in later life. I should add that there is no possibility of an operation to remove part of the gut as the whole of the gut is affected.
Good Morning Wednesday 24th June 2026



