Hi there, here's a link to an article about sweat tests (it's an easy and quick read.)
<a target=_blank class=ftalternatingbarlinklarge href="http://understandingcysticfibrosis.blogspot.com/2007/05/how-sweat-test-works.html
">http://understandingcysticfibr...test-works.html
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Sweat tests used to be the "gold standard" for determining CF, but these days the more reliable test is to have a genetic test done. When you're looking at the possibility of something as serious as CF, get a second opinion if possible. False positives are less likely with the sweat test than false negatives, but you never know.
The full panel from AmbryGenetics is the most comprehensive genetic testing, since it looks for more than one "flavor" of the CF gene.
Cystic fibrosis has its ups and downs. Sometimes people can go through periods where they have more digestive issues than respiratory ones, but even that is caused by the thick, sticky mucus.
The antibiotic, Levaquin is a very effective antibiotic. I've been on it a number of times and it has worked well to wipe out my infections.
Welcome to the site, I hope you'll get the answers you are looking for here. There are lots of great members who have a wealth of experiences and information to share about cystic fibrosis. Be sure to check out my site where I have posted a number of articles about cystic fibrosis. <a target=_blank class=ftalternatingbarlinklarge href="http://understandingcysticfibrosis.blogspot.com
">Http://understandingcysticfibrosis.blogspot.com
</a>
Regards,
Lauren
