sunshine07
New member
I am new to his site and have a question regarding my daughter. She is 7 months old and was diagnosed with CF through the newborn screening program. She had 2 sweat tests done in which both came back low borderline. They then decided to do the full genetics test through Ambry and it came back that she has I1051F & DeltaF508. They diagnosed her with CF Variant. We have been told that the I1051F has never been seen before and they don't know if this is a real mutation or a non disease causing variant. She is completely healthy. No problems or symptoms at all. She is not on any meds, but does go to the CF clinic every three months for preventive measures. My question is does anyone know of a situation like ours? We take one day at a time and hope for the best. But of course we realize that only time will tell.