Hi Everyone, Here in the UK we have a young Ostomate called Hannah Witton who has been blogging about her battle with UC. She has suffered with the illness most of her life and in Jan she had surgery. Just seen her on breakfast TV this morning talking about her journey. We have a young member of our own going for surgery shortly and it would be worth looking at this girls story. I was going to post a link but it brings up a lot of unwanted items, but any one interested Google Hannah Witton.