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Hello from Ireland

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Hello Everybody,

A friend of mine in work sought out this website, cfparents, for

me so I only just signed on yesterday.

I have been reading some of your stories and they are all so

interesting and some very funny about the eating or over eating

should I say!!

I have three beautiful girls, 10, 8 and 5.

My eldest girl always suffered with asthma and chest infections

and was always really weak and I was always coaxing her to eat

etc. etc. Last year after years of bringing her to our local

doctors, I finally got to see an asthma specialist, well the rest

is history. At 9 years of age, he told me she had what was

called Cystic Fibrosis. Needless to say my world just fell apart

and is slowly coming back on line. It's been a year of learning

and trying to understand the illness and all that goes with it.

At least I know now what's been wrong with her all these years.

With the right antiobiotics and enzymes she looks better than she

ever looked in her life.

My other two girls were tested and are fine.

It's great to be talking to other parents. I feel so isolated

sometimes, like I'm the only CF parent in Ireland and I've so

much I want to talk about.

I'll go for now. Hope you all have a nice weekend.

Ella.

For more information on the C&C Group visit http://www.candcgroupplc.com

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