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.
Bonnie Blue the MSM should stop all reporting.



