<<Disclaimer: Verify this information before applying it to your situation.>> After 11 months of seeking a diagnosis for severe upper abdominal pain which started 6 months after going gf following a biopsy diagnosis of CD, I was finally referred to a GI in a major State hospital in Melbourne who stopped looking at biliary tract disease and sent me off for a nuclear medicine gastric emptying x-ray. Bingo, the x-ray showed that I have delayed stomach emptying (Gastroparesis). I don't know how to express the way I now feel except to say that I feel "real", authentic. I suspect that gastroparesis is somehow connected to my CD. Perhaps my stomach was accustomed to emptying into a smooth small intestine without effort and now that the folds and hairs (villi) have returned the stomach has to work a lot harder to empty ( a second biopsy 6 months after original diagnosis revealed that my gf diet was working and my small intestine had returned to normal). (I do not have diabetes with which Gastroparesis is often associated.) Does anyone have any experience/information re Gastroparesis and CD? I have been prescribed Cisapride tablets to be taken prior to meals. Could this condition be connected to a deficiency of digestive enzymes? Is there something else I can be doing with my diet to treat this. Yeah, at last I will get well. Persistence and self belief have seen me through this as well as support from my family and employer, and the generous contributors to this List. Thanks Kathy Robison Albury, Australia