Our experience with CHOP was not as great as the others who have posted but we did not use them to the extent they have. They did my son's sweat test (borderline) and drew the blood for his genetic screening. His results were interesting with one 5T variant mutation and another that in most people have been asymptomatic. When the very kind nurse called me with his results, she said "as far as we are concerned, he does not have Cf." They never saw him.
Based on the recommendation of family member who has a son with CF, we took him the their CF clinic. They did a thorough history review and a multitude of tests and looked at that information (esp.his chest x-ray and PFT results) in the context of his genetic results. They did diagnose him with a CF variant and started him on enzymes--which are doing their job. EVeryone seems to agree that diagnosing CF is a clinical decision and I don't think CHOP got that right.
Based on the recommendation of family member who has a son with CF, we took him the their CF clinic. They did a thorough history review and a multitude of tests and looked at that information (esp.his chest x-ray and PFT results) in the context of his genetic results. They did diagnose him with a CF variant and started him on enzymes--which are doing their job. EVeryone seems to agree that diagnosing CF is a clinical decision and I don't think CHOP got that right.