Cystic Fibrosis
Sunday, January 24th, 2010 at
5:41 pm
rajjas asked:
this is a nice little video that a friend put together as a personal project because his daughter has CF.
Tagged with: Cf • Cystic Fibrosis • Personal Project
Filed under: Cystic Fibrosis
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ive got cf , diagnosed at 1 , im 15 now
I dint have CF but looking at your comments made my day… DONT EVER GIVE UP
haha me too! its the best thing!
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!!!!!!!!!!!
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
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 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
my boyfriend has Cystic Fibrosis and he is 15. he was diagnosed with Diabetes in January ’09. everyday for him is a struggle and i’m scared to lose him. i hope someday soon we will find a cure for both diseases.
this is a awsoem viid i love it when i was born my intestins expoled and i was diginosed with CF although i go though it every day i wish i i could help others to get them though it ! but the thing i **** the most it all the coufing !! sry i kind got off topic but i love you all for going though it with me !!!!! thanks
good luck with your lung transplant… i will be praying for you!
im lucky i as diagnosed when i was 2 months old^^ im 14 now and my doctor says im one of the healthest cf kids shes ever seen…but thats only becausr i was diagnosed at such a young age-_-
This is very good video. Brought tears to my eyes, because I can relate to those wishes. I was diagnosed when I was 15 with CF. I’m 18 now and everyday is a battle. I’m scheduled for a lung transplant next year and I’m looking forward to it! Wonderful video and I pray for your friend’s Daughter.
Thanks for sharing.
my best friend passed away 7 months ago from cf. without a doubt the hardest time in my life. seeing what he went through, i pray for everyone with cf and pray for a cure.
im 14, and i also have cf, amazing video.
I feel your pain! My best friend passed away from CF in 2007.
Please help!!
amen to that!
i doubt you husband will have cf too. the only way your child can have it is if you erm..”made the baby” with another CFer. i have it and i’m 13! diagnosed at 7 months old
=( I was tested for cf, cause I’m pregnant, and today they told me I am positive..don’t know if my husband is positive or negative….I’m scared to pass it onto my child!!
Google: Lung Transplant Bradenton, and you’ll find an inspiring story about a CFer who had a double lung transplant.
this is amazing. i have a close friend with cf, and i pray everyday we find a cure!