Hey everybody, I'm a 30 year old man with crohns disease. Diagnosed September 2009 after a small bowel resection. I had symtoms since 1995 when I had multiple surgeries after a ruptured appendix. From 1999 up until surgery I'n 2009 I had migraines on almost a daily basis along with wart like spots on my arms and peritoneal abcesses. I have to say I was relieved to finally know what was wrong after the last surgery but I'm finding it hard to deal with lately because of the numerous flare ups I've had this past year. The constant changes I'n health are the hardest thing to deal with for me. One day feeling strong and perfectly healthy and the next day hardly being able to get out of bed is enough to drive you insane. Its kind of like Jekyll and Hyde, two totally different people. I'm glad that there is a forum like this where we can understand each other's problems. My heart goes out to anyone afflicted with this disease. I know how it is to have a disease that few people understand, a friend of mine still asks me what's wrong when I have a pain I'n my abdomen or I get nauseated, I just say nothing because I get tired of saying my stomach hurts. I am thankful for the good days though and glad to have this site.
It could be worse.
It could be worse.