I've been reviewing all of the threads to find someone else who experiences nausea, not from food or eating, but from the PEG. I'm sure I'm not the first!! Having the long tube on my stomach tube, I returned to the GI doctor because it was extremely painful. He loosened the connection between the inside of my stomach & my outside skin by about an inch and started me on 2000 mg/day've been on Keflex for an infection. Maybe I'm just sensitive but I find any movement of the tube inside my stomach to be quite nauseating. I was told that I'd be able to return to regular activities but doing anything that requires movement is miserable. Sometimes I feel like a crybaby which is totally not me. Anyone have any suggestions??