My son is 5 weeks old today. He had a blood dna test done at 2 weeks old and we were told he had one abnormal cf gene. We then had a sweat test done and his numbers were borderline at 40.9 and 44.3. We are now awaiting results from an expanded dna test. However, his doctor keeps telling us he believes our son will be a symptomatic carrier. Has anyone else ever heard of this? Neither my husband or I have a history of cf in our families, so we are not informed on the subject at all. He weighed 6lbs at birth, weighed 5lbs 7oz at 2 weeks and now weighs 7lbs 9 oz. They tested him for CF because he had a meconium plug at birth and because of the weight loss. So I guess I just do not understand how he could have symptoms but not the disease. Thank you so much for your time.