Hello, my name is Meredith and I'm 31 years old. I was diagnosed with Crohns Disease in 2010. Up until then, I was really healthy. Never any problems what so ever. Then one day- boom. It hit like a ton of bricks. I thought I was dying. I had awful stomach pains, diarrhea, and couldn't keep anything down. I practically lived in the bathroom! At first, I thought it was something I ate or some type of stomach bug. After 3 days I finally went to the doctor. Nothing came out of that, he said a bug was going around so I went back home to be miserable. A couple more days went by, and I was getting worse. It literally felt like a rat was in my stomach clawing it's way out. I knew this was something far worse than a "bug"! I went back to the doc and he sent me to a gastro doc. Boy, was he my savior! It took some time and a lot of tests to diagnose me. I was admitted to the hospital with severe dehydration and Crohns flare up. I stayed about a week and was released. I was taking what seemed like 100 pills a day but nothing was working. I never felt good. I lost 30 lbs and just looked "sickly". Finally my insurance approved me for Remicade infusions. I started out going every 8 weeks but I still had flare ups. My last flare up was last May. Was admitted to the hospital again and acquired pancreatitis from all the prednisone I was receiving. I'm now on Remicade every 6 weeks and have not had any major problems since. I guess I've been lucky so far. This is a nasty disease and I feel for all of you who have to go through this. Its depressing!