Thank you so much for all your stories/advice, my daughter's sweat test was really low, but her symptoms just urk me, so I insisted on the genetic testing, plus her older brother had some type of cell blocker in his biliary tree that doesn't work properly ( he has a lot of digestive issues), we did the sweat on him a few yrs ago b/c of this, and it came up real low to. I just took him for the sweattest & never questioned CF b/c noone in our families have it. But now here I am 2 yrs later, and it came up again. The only thing is, when my son was tested, I had no clue, and lathered him with body lotion after his bath, then went for the sweat test. So now I am really bothered as to the accuracy of it. I never thought about it until my daughter started going through some reoccurring problems (digestive & respiratory), and the suggested the testing.
So now as I am awaiting these results, I am trying to find things that could help minimize the eyes from doing this. Even if it isn't CF, I have got to figure out something to help them.
Does anyone think that eye drops (like visine) helps the eyes - or anything else simple over the counter that I could try?
As for her sweating - she is soaked in her sleep, but never sweats during the day or anything for me to notice sweat marks around her hair, plus her hair is white/blond, so I have never noticed anything.