Pending the outcome of our next pulmo visit, which is within the next week, it looks like we are going to Ambry for tests that we will have to pay for out of pocket. It aggravates me that people have to fight so hard to get testing done. Having a kid sick for so long and no one can tell you what's wrong, yet there are tests availcable that docs just won't order.
I wonder how many people are cf positive and are never diagnosed correctly. Just for curiosity's sake, how many of you have had "normal"(below 40) or borderline sweat tests and still have been found to have a positive cf diagnosis? I'm hearing of more and more people that this seems to be the case with. Interested to hear back. Thanks, T
I wonder how many people are cf positive and are never diagnosed correctly. Just for curiosity's sake, how many of you have had "normal"(below 40) or borderline sweat tests and still have been found to have a positive cf diagnosis? I'm hearing of more and more people that this seems to be the case with. Interested to hear back. Thanks, T