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I have Cf, It is VERY sad! I am in the hospital right now because of it! I have a picc in right now!

i dont have cf but my friend kendra did she died in last year at 15 i tried her vest and it hurts so bad because she has to doit 3 times a day sum times for a long time she dident let cf get too her she barrel raced all the time

legillizgay 8 months ago

im 18 with CF. going to college. have a girlfriend and a job. things dont get easier. but gotta be postive.

anthonythedunkmaster 1 year ago

they need to change cf from cyctic fribrosis to cure found

taylorchavis1 1 year ago

I'm glad that I started dating this girl named Nicole, because without her brothers suffering due to CF I would have never thought about helping out all of the innocent lives. I'm now trying to raise as much money as possible to go towards finding a cure. God bless you Matt, and all of the others suffering from this genetic disorder.

NoyeRox 1 year ago

Thank you so so much for this video

SweatySkate 2 years ago

thanks so much for this video. i am 13 and have cf. it is very difficult to deal with bless you all

Horsegal143 2 years ago

Great Video...I love the song, My Wish, it was one of Siobhan's (my niece) favorite songs. She passed from CF at age 27, June 24, 2008. We are still hoping, praying, and working for a cure. God Bless all who suffer from this disease.

kryan364 2 years ago

This is too my beautiful Kelly. She unfortuantly suffured with Cystic Fibrosis, all her 18th life, you wouldn't know how much pain she was in. She hid it all her life. She was deffinatly the prettiest girl by far, she smiled everyday knowing she had a short life too live, but she lived too the full. She was told she wouldn't make it, but she was a hero and made extra months. She was able too celabrate her 18th. Rest in peace angel. Sleep tight, im always with you. I love you princess x

AmieLouise89 2 years ago

i'm 13 and have it!!

1moe7 2 years ago

Thank you for the information!! my nephew Nathan Contreras has CF...he is 4... you can see his video on my site...

I know this is super hard to deal with...plus huge medical bills!!!

Jallulah 3 years ago

Inspiring, we'll find a cure.

BANA0907 3 years ago

I love this video. It shows how it really is. I have CF, and im 11. Its hard trying to keep up with a social life and keep healthy. my mom is a single mom of 4 kids, NONE of which are 'perfectly healthy' i have CF, osteoperosis, diabetes, chronic sinusitis, and other things. my brother has severe asthma, and my sis and bro have ehlers downlose syndrom... my friends cousin died of cf at 18, and her other cousin still has it. i LOVE allie! she helps me through it all, and thats not easy to do!

puggable 3 years ago

this comment is really sweet. i am 13 and I have cf. stay strong! and one o f the most importatant things I have learned from cf is to live lie to the fulleset and always have fun, and try not to complain and just hang out and go places, and respect that your alive! just think- we are all lucky because 30 years ago ppl w/ cf rarely lived past two.

your comment touched me and you and your family, and your freind's cousins will be in my prayers! god bless you

gemmasinger 3 years ago 2

Thank you for this video! My son is 10months old and is a carrier of cf but has had a serveraly weakend immuned system a simple cold keeps him sick for weeks and i still have no awnsers why! they say he should have any symptoms because hes just a "carrier" but he does

mommy62287 3 years ago

You're right, Im 16, and when i feel sick, i dont look it. When I had lung infections i looked healthy, so a lot of kids thought I was lying.

Because of CF I had to have a double lung transplant, I got my transplant on August 7th, 2007. It's been over a year, and everything has CHANGED, no more breathing treatments, no more worrying if my lungs were going to let me play volleyball at a HS game, now, i dont have to worry about all that now.

kEViNJoENiCKrHOt 3 years ago