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Hi there, Iv just read your entry and identifiy totally with how you feel right now! My daughter was diagnosed eight months ago with cystic fibrosis and she is just seven. My youngest daughter who is three years old has had a normal sweat test, we waited five weeks for that to be organised and...

Hi there, Iv just read your entry and identifiy totally with how you feel right now! My daughter was diagnosed eight months ago with cystic fibrosis and she is just seven. My youngest daughter who is three years old has had a normal sweat test, we waited five weeks for that to be organised and...

Hi there, Iv just read your entry and identifiy totally with how you feel right now! My daughter was diagnosed eight months ago with cystic fibrosis and she is just seven. My youngest daughter who is three years old has had a normal sweat test, we waited five weeks for that to be organised and...

Hi Meghan, My daughter was diagnosed seven months ago, and life has been kind of foggy ever since. My husband and I are both very positive people, and I guess being brits its all very stiff upper lip. However, deep down the feelings of fear and I think grief are at times overwhelming! It is...

Hi Meghan, My daughter was diagnosed seven months ago, and life has been kind of foggy ever since. My husband and I are both very positive people, and I guess being brits its all very stiff upper lip. However, deep down the feelings of fear and I think grief are at times overwhelming! It is...

Hi Meghan, My daughter was diagnosed seven months ago, and life has been kind of foggy ever since. My husband and I are both very positive people, and I guess being brits its all very stiff upper lip. However, deep down the feelings of fear and I think grief are at times overwhelming! It is...

Hi Jayne and Callum, I wish you all the best with the sweat test tomorrow, my daughter was diagnosed Seven months ago, although for years Iv had issues with her poos. They hardly ever flushed away, were not just smelly but quite putrid, also they also had what I now know was a fatty content...

Hi Jayne and Callum, I wish you all the best with the sweat test tomorrow, my daughter was diagnosed Seven months ago, although for years Iv had issues with her poos. They hardly ever flushed away, were not just smelly but quite putrid, also they also had what I now know was a fatty content...

Hi Jayne and Callum, I wish you all the best with the sweat test tomorrow, my daughter was diagnosed Seven months ago, although for years Iv had issues with her poos. They hardly ever flushed away, were not just smelly but quite putrid, also they also had what I now know was a fatty content...

Many Thanks for that! Iv been looking at this site for a while now, and Im blown away by the amount of truly inspirational individuals! You are right, it is a unique community! Im comforted by the fact there is somewhere to share experiences and emotions!

Many Thanks for that! Iv been looking at this site for a while now, and Im blown away by the amount of truly inspirational individuals! You are right, it is a unique community! Im comforted by the fact there is somewhere to share experiences and emotions!

Many Thanks for that! Iv been looking at this site for a while now, and Im blown away by the amount of truly inspirational individuals! You are right, it is a unique community! Im comforted by the fact there is somewhere to share experiences and emotions!

Hi there, my name is Cathy Williams and I live in Plymouth, uk. I have two daughters, Annie who is seven and Olivia who is three years old. Six months ago Annie was diagnosed with cystic Fibrosis, after years of concern over growth and development, wierd poos, and what we were told was asthma...

Hi there, my name is Cathy Williams and I live in Plymouth, uk. I have two daughters, Annie who is seven and Olivia who is three years old. Six months ago Annie was diagnosed with cystic Fibrosis, after years of concern over growth and development, wierd poos, and what we were told was asthma...

Hi there, my name is Cathy Williams and I live in Plymouth, uk. I have two daughters, Annie who is seven and Olivia who is three years old. Six months ago Annie was diagnosed with cystic Fibrosis, after years of concern over growth and development, wierd poos, and what we were told was asthma...