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2 yo son just diagnosed

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From the time my son was 3 weeks old he has been sick with some sort

of respritory problem or another and has always had real bad

diarhea. We have, for 2 years now, tried to find out what was wrong

with our baby. It finally took a trip to the ER just before x-mas

for them to decided to test him for CF. I have brought this up with

my dr.s 2 times in the last year (testing him). I was lead to

believe that it was am impossible diagnosis because we had no family

history. To my sadness this is not a true assumption. This past

wednesday we finally had his sweat test and by that afternoon we knew

the results. I am completly shocked at the results. Thursday was a

long confusing day with all the info I recieved from his Dr.s.

Needless to say I am still confused and struggling through this

initial dose of info. Any tips on how I can grasp all this info and

remember the important things would be wonderful. I would appreciate

all the help I can get from anyone who knows what this is like,

because I feel like my world just fell apart.

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