Like everyone here, my story is a long one. I was diagnosed in 1990 at age 23 after my colon ruptured, nearly killing me. Nine months and three surgeries later, and I was sent back out into the world, but obviously life with Crohn's is tricky. I feel like I'm one of the lucky ones, despite the fact I still have persistent symptoms (stomach discomfort, frequent bowel movements, occasional fever, etc.).
I make my living as a writer, and for years people had told me I should write a book about my Crohn's experience. It was really cathartic. I see many of you writing about your experiences in these forums -- glad there are support systems like this now. I had nothing of the kind when I was diagnosed, so I felt very, very alone. Cheers to everyone who keeps fighting the good fight.
I make my living as a writer, and for years people had told me I should write a book about my Crohn's experience. It was really cathartic. I see many of you writing about your experiences in these forums -- glad there are support systems like this now. I had nothing of the kind when I was diagnosed, so I felt very, very alone. Cheers to everyone who keeps fighting the good fight.