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Hi everyone!

Well as this is my first post I will introduce myself a little Smile

My name is Kel and I'm a 24 year old female with Cystic Fibrosis. My younger brother has it too and so did my sister (She died from cot death when I was 2.)

Up until the last couple of years I have been really lucky and never had any major sickness or hospital admissions. I've only just recently been put on Creon because my food just isn't digesting properly anymore.

Anyways I was hoping to find some other CF'ers around to have a chat too! I only know a couple here and there! Big Grin
Welcome Kel Smile Maybe you can share some stories you have come across about those suffering from CF and the affect it has on their/your lives.

healthau Wrote:
Welcome Kel Smile Maybe you can share some stories you have come across about those suffering from CF and the affect it has on their/your lives.


I don't really have many stories. I am so much luckier than other people with CF because the only thing I have had to put up with up until now are the odd chest infections.

For people that don't know what CF is, here is a link with some info for you!

Cystic Fibrosis Information

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