Cystic Fibrosis

I dint have CF but looking at your comments made my day... DONT EVER GIVE UP

haha me too! its the best thing!

i was diagnosed at 6 months...but had problems from day 1...doctors wouldn't believe my parents and said that i was just a small baby who had really disgusting nappies and cried a lot lol...now i'm 18 and my cf is better than it has been but my lung function is only 40%...so everyday the one wish i have...is to be able to breathe...and i wonder what it's like to be able to smell fresh air and go up the stairs without having a coughing fit....but i am hopeful of a cure...i just hope its here soon

hi sarah, i am also 13 and have cf since i was born. your comment about never giving up made me smile! x

it made me cry. Im sarah im 13 years old and i was diagnosed with cf when i was born. i was not suppose to live this long. ive lost a friend to cf her lost her fight. I am not going to lose my fight! i refuse to let cf kill me. tears are rollin down my face rite now. dont ever give up fight!

Hi girl,my name is Gaby,I am from Europe and i lost my sister 10 years ago from CF!Dont ever give up PLEASE!!!!!!!!!!!

Hi my name is Wondy and I am an RT.
I work at a children's hospital,taking care of kid's with cystic fibrosis.
They are all hero's.

My name is Cheri Taylor.
Im 14 in 3 weeks.
I was diagnosed with Cystic Fibroses at birth.
I love life and I try to do all my stuff right and good so i can live longer.
I was suppost to pass away when i was six.
For everyone who has it let's show everyone we can do it and be stronge
lot's of love to the kids out there who have it (:

i have cf and im 14 i was diagnosed at 2 years old im lucky to be alive, i really hope they find a cure need prayers