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Hello everyone...

My name is Jane. I am very glad to have found this list as we are still

in the " numb " stage here as we continue the diagnosis process. My

youngest child is 19 months old and wasn't gaining weight. She also has

asthma so we went for a sweat test. The result came out borderline so

we went back at did another test which came out much lower but they also

took blood for a genetic screen. I got the results of that screen

today. They looked for the top 30 mutations (of the 900 possible CF

ones) and found she had one of these. Now apparently they start the

search for the second gene using my and my husband's DNA also. The

clincher here is that 2 days before we had the results of the first

sweat test, I found out I was expecting another baby. So the stress

level is a little high 'round here. We are back at the CF clinic next

week and will talk to the geneticist about the siuation.

Has anyone else had such a confusing time trying to get a diagnosis? I

thought CF would be fairly clear cut to detect.

Thanks,

Jane, wife of Tom, mom of wocf, Tony wocf, wocf, Meredith

wocf, Eleanora maybe wcf and one on the way.

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