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Jack's sweat test

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Hi. I just got word FINALLY that the sweat test came back NORMAL. I want to

be sure and thank all of you so very much for all of your help. I understand

your quest to spread awareness as I do the same for the condition that my son

Max was born with. I will keep this CF family in my prayers and I am praying

for a cure for all of you. God Bless all of your children and your families.

You are such strong dedicated parents, I am honored to have met and been

able to communicate with you.

The Pulminologist says he will try to find a way to keep Jack's breathing

regulated so he doesn't have to " struggle for air " on occassion and he will help

us get through this (I hope) We will work on getting to the bottom of all of

this mucus. We will see him this week.

Continue to be as strong as you are and keep fighting this disease. You are

all heros to me. God Bless you all!

Hugs to you all - Amy

Click to read " Max's Story " <A

HREF= " http://www.cappskids.org/CAPPSCranioKidMax.htm " >CAPPS CranioKid Max</A>

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