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hi steve just writing to say well done it sounds like you have worked very hard but yet again all cf victims have to work hard

hey emily you do not know me but i've been reading that you are in hospiital and i hope that you get better soon also my name is rebekah and if you would like to email me you can because i love to make new friends my email address is cf.info@livethelife.com

yes you can be born wif cf

hey brain you do not know me but my name is rebekah i'm 15 and i live in new zealand and you sound really cool here is my Email address cf.info@livthelife.com can not wait to hear from you bye bye <img src="i/expressions/face-icon-small-happy.gif" border="0">

The way you are diagnosed with cystic fibrosis is the doctors give you a sweat test and if your sweat has lots of salt you have it and you also get a whole heap of blood tests at birth but all babies at birth get this treatment so if you do not have cystic fibrosis then your test comes back...

hi i'm 15 and four months ago i lost a friend to CF and it as been so hard with him not here because i have known him for about 10 years and when he told me that he was dying i told my self that he would get over it but about 2 months later i was at school and one of my mates told me that he...

hi i read your thing on the internet and i know what you are talking because my mates do not get what i'm talking about also they do not understands what i'm on about. i hope your liver transplant went well. i have also have a surgery on my left hand-side i had an portacath placed in and after...