J
Jfrank
Guest
Hello I'm new here. I was diagnosed with crohns disease in my small bowl a little over a year and a half ago. I was diagnosed when I had a flare up after a colonscopy. Despite some days of cramping and pain I always considered myself lucky because my GI told me I had a mild case. At first I was put on Asacol and then was switched to Pentasa and put on the maximum daily dosage. The past few months I had a lot of cramping and a few weeks ago I was hospitalized for the first time. I was put on 40 mg of prednisone and i am now starting to ween off of it. I am now taking 30 mg and am still taking the pentassa. I am currently seeing a new GI because we were unhappy of the care that I received when I was hospitalized. This new GI who is suppose to be very good and associated with Mt. Sinai is retesting me because he doesn't think there is conclusive evidence of crohns diesease from the past colonscopy, cat scan and upper GI tests. He said that just because it shows that my small intestine is inflammed does not mean it's crohns although it is likely since i have a family history of IBD. I'm just kind of nervous to go through the colonscopy again because of the flare up I had from it the first time. I'm first getting a gi series of my small bowl done on thurs. i'm hoping i don't have to get the colonscopy done. I'm just getting very frustrated because my stomach is still very sensative. I have been following weight watchers the past few months and doing very well on it but it is starting to get difficult with following a low residue diet. I also find that I go through periods of being extremely hungry which I think is from the prednisone. If anyone has any suggestions on food or anything else i would really appreciate it.