heatherrose415
New member
I have been here before, quite a while ago, going through the testing process for CF. My sons sweat tests were 41 and 31. They did the full ambry genetics test and found nothing except he is 7T/7T poly T Variant.
He has no lung issues, just pancreatic insufficient. He is still having a VERY hard time gaining weight, he is still off the charts despite the enzymes and tagamet for stomache acid.
They upped his enzymes to the maximum amount he can have for his weight.
His GI Dr. at Stanford CHildrens Hospital said that "A Typical Cystic Fibrosis diagnosis is in their back pockets"
Has anyone been diagnosed before without finding any known mutations??
He is 2 1/2 and has been "sick" since he was born.
They are also going to test him for Shwackman diamond syndrome.
He has no lung issues, just pancreatic insufficient. He is still having a VERY hard time gaining weight, he is still off the charts despite the enzymes and tagamet for stomache acid.
They upped his enzymes to the maximum amount he can have for his weight.
His GI Dr. at Stanford CHildrens Hospital said that "A Typical Cystic Fibrosis diagnosis is in their back pockets"
Has anyone been diagnosed before without finding any known mutations??
He is 2 1/2 and has been "sick" since he was born.
They are also going to test him for Shwackman diamond syndrome.