Hi, everybody:

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Do you know of any forums for Cystic Fibrosis children who had transplants at a young age? I feel really, really bad not getting any answers, even if I do realize this forum is not very busy. I believe some parents (with their family, their friends, their coworkers, their neighbors, or some of their acquaintances) using this thread about children's health must know someone, even if it is only one person, who has a child with Cystic Fibrosis who can give me some help or advice. After all, Cystic Fibrosis is not that rare a disease; it is even more frequent than RSD for example. RSD patients get answers, so why not Cystic Fibrosis patients and their caregivers, when these patients happen to be children? Please, someone, help my baby! It is not because my baby had transplants that he is out of danger. After all, while taking immuno-suppressants, he could easily catch a microbe, virus, or parasite that would kill him in a cinch because his immune system is suppressed.*edit*