Hi All. I'm Daniel and 16 years old and I was diagnosed with Crohns just over a month ago. I have been on this forum for a few weeks now and have finally got the opportunity to write down my story.
As Crohns goes I consider myself quite lucky - I have never suffered from any bowel symptoms. In fact it was a culmination of a few small things that led to my eventual diagnosis. It all started about April last year when, after a week holiday with my friend, my Dad noticed a very slight swelling in my right cheek; at the time I thought nothing of it assuming that it would go down over the next few weeks. But after about two months I had noticed that it hadn't changed so I went to the Doctors to see if there was anything wrong. From there I was sent to see an orofacial consultant where I had biopsies taken from inside my cheek - these came back to show that I had orofacial granulomatosis. From here I was sent to a paediatric consultant who looked at this and other symptoms (weight and height dropping off and a couple of perianal skin tags (these had not been causing any problems)) thought that it could possibly be Crohns, so I went and spoke to a gastroenterological doctor who set me up for a colonoscopy and endoscopy. Although these procedures didn't show up any visual problems biopsies revealed very slight inflammation at various points.
From that I have been put on a 6-8 week modulen diet (Half way through so far - woooo!) and I am also on 4g Pentasa a day. Next week I am due to have an MRI to have a look at my small bowel.
I feel quite glad that it has been caught 'early' as such but was just wondering if there is anyone out there who has experienced anything similar?
Cheers
As Crohns goes I consider myself quite lucky - I have never suffered from any bowel symptoms. In fact it was a culmination of a few small things that led to my eventual diagnosis. It all started about April last year when, after a week holiday with my friend, my Dad noticed a very slight swelling in my right cheek; at the time I thought nothing of it assuming that it would go down over the next few weeks. But after about two months I had noticed that it hadn't changed so I went to the Doctors to see if there was anything wrong. From there I was sent to see an orofacial consultant where I had biopsies taken from inside my cheek - these came back to show that I had orofacial granulomatosis. From here I was sent to a paediatric consultant who looked at this and other symptoms (weight and height dropping off and a couple of perianal skin tags (these had not been causing any problems)) thought that it could possibly be Crohns, so I went and spoke to a gastroenterological doctor who set me up for a colonoscopy and endoscopy. Although these procedures didn't show up any visual problems biopsies revealed very slight inflammation at various points.
From that I have been put on a 6-8 week modulen diet (Half way through so far - woooo!) and I am also on 4g Pentasa a day. Next week I am due to have an MRI to have a look at my small bowel.
I feel quite glad that it has been caught 'early' as such but was just wondering if there is anyone out there who has experienced anything similar?
Cheers