YouTube - Broadcast Yourself.

My cousin had CF but she died when she was 14..6 years ago

He is a good looking boy.I have four grand boys who have cf and my daughter is raiseing them by herself.Her husban was killed in a car wreck after the twins were born.

GoodOBoy757 3 years ago

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For more information on cystic fibrosis, simply type in Gibson Vance promoting Cystic Fibrosis in your youtube search engine

beasleyallen 3 years ago

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When you get to the American Express Member Project home page type UZHKO0 into the search box...it will take you right to it.

Come on people, $1.5 million could be AWARDED for ORGAN DONOR AWARENESS if we can win the VOTE!

PLEASE TAKE THE TIME AND PASS THE WORD

organdonor5 3 years ago

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There is a great project to increase DONOR AWARENESS that ends Septemebr 1, 2008. American Express (credit card company) will fund the project with the most votes and I would LOVE for it to be the DONOR AWARENESS project.

It was written by an 18 yr old girl that received a transplant and is living with CF cystic fibrosis.

GOOGLE IT. It is called Member Project "Second Chances" Mobile Organ Donation Awareness.

Please VOTE FOR IT, pass the word to everyone and increase DONOR AWARENESS!

organdonor5 3 years ago

my mom has CF and so did my uncle he died they are amazing and i love them.

Tory584 3 years ago 2

i am 21 years old with CF i had a double lung transplant when i was 18....i was not expected to be here at all. CF does suck but i also agree that i would not change having it for anything..it has made me who i am, i am now a youth worker and also work with teenagers who are chronically ill. I do public speaking for CF and for organ awareness....life is a gift and every expereience whether good or bad is a learning and growing experience

silvadodge86 3 years ago

I am a mother of a son who died age 17 of CF in 2004. You are right - CF makes a person who they are and I hear of so many people with CF whose disease has given them great strength. Take Gregory Lemarchal for instance - the French singer who died last year age 23 (there are loads of vids on youtube). My son's favourite song was 'Nothing Else Matters' - For ever trust in who we are and nothing else matters (Metallica).

soopersue 3 years ago

nothing else matters is my favourite song too...metallica are my fave band

silvadodge86 3 years ago

You are the same age as my son would have been. Glad to see young people still like the ageing rockers! David's band played NEM at his funeral. (David was a drummer).

soopersue 3 years ago

ur amazing

i hv cf 2

lifelovepeaceGP 3 years ago

Stay tough I know it is hard but I am 23 years old and I have CF. I have alot of friends who are even older and I see alot that has improved over the years. I wish you the best.

ehsnrgs927 3 years ago

thank you for your story. I'm praying for all CF people around the world for a cure.

chieftalentofficer 3 years ago

We loved the pictures..he's so adorable. Our 12 year old daughter has cf. we believe its all about the maintence..(thats what we call the treatment, meds) she has a 4600 calorie intake a day. that really helps. half comes from ensure plus drinks. keep up the fantastic work, mom and dad we know it can be hard at times, but we all know its worth it! enjoy him lots! messybubbles's family.

messybubbles 4 years ago

I am 12 and I have CF! IT SUX! I h8 the vest....

although it makes me feel better.... :)

BEST WISHES TO YR DAUHTER! PEACE

luv

GEMMA xoxo

gemmasinger 4 years ago

it doesnt suck, it makes you who your are

surfnguitar74 4 years ago

do u have it, it does suck, mucus is blocking your lungs and you can barely breathe and ppl make fun of u cuz u couph up grose stuff... IT SUX

gemmasinger 4 years ago

yes i do have it but if you have real friends that you can tell them about it, then they wouldnt do that

surfnguitar74 4 years ago

Yes, i do tell them about it, but its the "bullies" at my school who make fun of me about the mucus and being small and ppl say i am bulimic (I AM NOT) cuz I eat a lot of stuff, I am A PIG! lol and yet i am so skinny, ppl make fun of me. CF SUX!

gemmasinger 4 years ago

okay, whatever i am never going to meet you never going to be in contact with you

so i am not even going to argue

surfnguitar74 4 years ago

dnt take any notice of them

they r jealous coz u can eat urself sick and not get fat... while they weigh a ton.

lifelovepeaceGP 3 years ago

i have cf, i'm 15 years old. if you have real friends that care about you, all the other people don't matter. if they're going to make fun of you for a lung disease, i feel very sorry for them. they don't know what we go through every day, they don't know how much pressure is put on us day in and day out. just know, you're not a freak. just because we cough up more stuff than they do, it doesn't make us gross or weird. it makes us who we are, and we're something beautiful.

believeex3 4 years ago

thank you! u ROCK MY SOX!

gemmasinger 4 years ago

now, i have new firends and they are amazing people.... they dont make fun of me.... :) YAY!

gemmasinger 3 years ago

i have cf!!

jadehorgan 4 years ago

Hi jake im 32 and i also have cystic fibrosis with other major medical condions i really liked how you shared your photos with everyone that was very kind of you if you would like to email me you can at talk to you soon hope you are having a good summer

CFDLW 4 years ago

Hi everyone ..Im 29 Yrs old with CF and i can say that somtimes life is not easy,, But never give up hope and Faith, someday we will fine a cure for it ;)...have a great day ....

rejmel 4 years ago 2

What do you mean its amazing!? I have cf and it sucks. I can hardly go to school anymore because they always send a wheelchair when i struggle for breath on the stairs!

lauren100289 4 years ago