My daughter was diagnosed at 2 weeks of age. She was born with a meconium ileus. We were seen by multiple doctors because we were in the NICU for a month. A Peds GI doc put her on actigall and I still can't figure out why. Is anyone else on this or has anyone heard of another CF baby on it? I don't want my daughter on any unnecessary meds, but if she needs than I want her on it. I just can't find any information anywhere about CF and this drug. We are going to this this Peds GI doctor tomorrow (hopefully for the last time)and I want some info before I go. Thanks!