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Hi all,

My name is Leah and I have a 19 month old son who has yet to be

offically diagnosed with cf. We are to go to St. Louis Monday and

find out results/or see if another sweat test needs to be done. Just

to fill you all in on him he was diagnosed with severe GERD when he

was 3 weeks old. At the age of 6 months he had his first surgery a

nissen-fundoplication. He has since had tubes put in his ears, had a

diagnoses of chronic sinusitus, a loose fundo, decreased motillity of

the esphogus, and a sliding hital-hernia.

His ped has started to do immune test and with some of the results

preceeded with the sweat test. It came back positive but she

considered it inconclusive. As of right now we are waiting to see his

gi who specializes in cf. We will hopefully now within the next week.

I was wondering if this story sounds familiar. I am new on this and

not to sure what to think. Any info would be nice.

Thanks

Leah

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