Hi everyone-
My fiance was diagnose last October, he is 20 years old and the gi thinks he's had CD for 15 years now... The reason they finally figured it out was he get these "abscess's" on his legs, they start out small, gradually get bigger with infection, at this point walking is very painful, and they burst making a nasty and painful mess. He was pretty much down and out for 3 days because of the last one.. One doc called them ulcers, the skin doc thinks its PAN (polyarterosis nodosa) the gi doc says it is chrones. The skin doc is the one that finally sent him to get a colonoscopy because a side affect of PAN is bowel issues... Anyone experience anything like this? They do seem to be better when the CD is under control, but he is on nothing at the moment, had to stop using 6mp becuase he was one of the lucky 1 in 200 that is allergic and got pancreatitis. The insurance is stalling about paying for the Humira, so we've been waiting for weeks to recieve that.. Just wondering if anyone knows or has experienced anything like this. It's getting out of control and the gi doc just tells us to wait for the humira... Not very helpful. Thanks!