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Adult WCF

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Hi Everyone,

Zach was only diagnosed 6 months ago. I hadn't met any adults with

cf until this weekend. We met a great lady who is 26 years old and

runs marathons! She is such an inspiration to us. She hasn't let

CF stop her from doing anything she wants and that is how we hope to

raise Zach. I had only met other parents who unfortunately were

very negative about the disease. I constantly heard about how many

vacations were spent doing tune-ups and that cf kids end up in

therapy because they hate their parents for giving them the

disease. Never did I hear how proud they were of their child. That

is why I enjoy this list so much. We can talk about the negative

aspects of the disease, but we can share the joys of parenthood as

well.

She has given me so much hope. I wanted to share that with all of

the moms with little cf babies.

Sara - mommy to Zach 19 months wcf

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