Hi I just recently found out that there is a very high chance that my 3 yr old foster son has cf. His sweat test came back high a few weeks ago and was tested again this week. We don't have those results back yet. He is very tiny, closer to the size of a 24mo old. He has had almost a constant cough since he came into my care 2 months ago. He also typically has very loose bms. And gets respirtory infections easily. He is such a great kid with a wonderful spirit the giggles and laughs just don't stop. I want to do everything I possibly can to take care of him, but at this point I know so little about the disease and only his social worker has been able to visit with the doctor up to this point, so I have very little information.to go on. Please help give me some ideas as to what I can do to help him. If he does have cf what will that mean for him? Any input would be greatly appriciated. Thanks FM