<<Disclaimer: Verify this information before applying it to your situation.>> I have noticed a number of people on the list who are parents of Celiac Disease children. Are any of these posters Celiacs themselves along with caring for the child's needs? I imagine that combination would really be a nightmare. Does the "fuzzy-mindedness" that so many mention as an adjunct to Celiac interfere with the overall care? I should think these parents would need a special kind of strength. It would be interesting to read how they set priorities and get everything done. Could some of these Celiacs, who are also caregivers, give us some inspiration and understanding into ways to cope? I find all the "connections" that are associated with Celiac fascinating. I think many of us could benefit from some insight into coping mechanisms. I have suspicions about two of my grandchldren. One (age14) has had, ostensibly, the best of medical supervision (Boston Children's, etc.) The other(age 4 1/2) is just thought of as a rude, disruptive, undisciplined child, AT TIMES. The girl who has had so much attention and money spent on her, has not fared well. She has multiple fractures, lethargy, and varying diagnoses from Chronic Fatigue Syndrome to possible Lupus. Neither child seems to come close to being Autistic. I worry about them. Worry solves nothing. The doctors think my being a Celiac is "incidental", and of no consequence. The little boy will probably end up in jail by the Second grade. Strangely, both are very attractive and socially competent. Who's to know? AMS