Added: Jun 14, 2007
From: rajjas
Duration: 1:52
this is a nice little video that a friend put together as a personal project because his daughter has CF.
Channel: People
Tags: breath children cystic fibrosis help lungs
believeex3 Says:
Nov 3, 2008 - i have cf, i'm 16. and i just got out of the hospital yesterday. it's hard to live with, but everyone; stay strong. you give the rest of us hope <3.
believeex3 Says:
Nov 3, 2008 - i have cf, i'm 16. and i just got out of the hospital yesterday. it's hard to live with, but everyone; stay strong. you give the rest of us hope <3.
tinkerbelljyt101 Says:
Nov 9, 2008 - this is really good, but if it wasnt for the logo at the end would have no idea this was about cystic fibrosis. i just dont get how "wishing" has anything to do with it.
hopeandwork Says:
Nov 10, 2008 - I am so sorry
hopeandwork Says:
Nov 10, 2008 - A cure will not find a cure by donating to the CF foundation. It is a fraudulant organization
hopeandwork Says:
Nov 10, 2008 - But not through the foundation. It is a fraudulant organization
Korianga07 Says:
Nov 19, 2008 - The Cystic Fibrosis foundation is a great organization, 90 cents of every dollar donated goes directly to cystic fibrosis research. I have CF and I know that this organization is one of the big reasons that we have made so much progress with medicines and the treatments. so please don't make comments like that because this organization really does help millions of people and we need it and we need people to know how great it is.
hopeandwork Says:
Nov 19, 2008 - The cf foundation origianlly may have been an upright company, They have since become rampant with fraud. Including Rober J. Beall. Are there some good people in the company? Perhaps. But know this as well; of a physician or clinic has received donations to be used locally only, the foundation will use threats and intimidation in order to force all donations to be sent to them. The CF foundation is not the only such company or organization.
hopeandwork Says:
Nov 19, 2008 - Scamdipharm's purpose is to rip off CF families who could use the funds they use on thier products for much better products at much lower prices. Scandipharm truly is a scam. May you and all cystic patients be blessed. But study and think out of the box created by the foundation.
crit639yourock Says:
Nov 27, 2008 - my sister died from cf she was 19 she was only supposed to live too 10
snoll2222 Says:
Dec 1, 2008 - i have cystic fibrosis its hard!!!!!!!!!!:((((
snoll2222 Says:
Dec 1, 2008 - i have cystic fibrosis am 13 its hard getting needles surgreys stayinin the hospital so please be helpful and help us find a cure!!!!
wearefun9 Says:
Dec 5, 2008 - omg my best friend has C.F. and she is struggling right now and that just made me sob like a baby thx for posting that
livelaughlove10101 Says:
Dec 8, 2008 - omg i love this video!! i have cf and it made me cry. but some day cf will stand for cure found and it can all be over <3
summerbabbbe Says:
Dec 11, 2008 - This made me cry last year me and mah friends rashed 1000$ for CF because my friend has it. she is really sick now and I want her to get better fast. We love you Anna, get well soon.
rgandy23 Says:
Dec 11, 2008 - horrible disease, doctors thought my brother had it as a newborn. luckily he did not. he would probably have barely made it to his 20s. keep all people who have this in ur prayers!
willdafergman Says:
Dec 12, 2008 - My sister has CF, she's 12. I feel so bad for her. The things that poor girl has to go through everyday... There truly is no God, for how could he intend for people to suffer in this way. Videos like this make people forget the little problems they get in life that they all complain about, and think of people who really do deserve their thoughts.
1moe7 Says:
Dec 13, 2008 - believe it or not, I actually know a guy who has CF and he's turning 50 soon!! and another guy he's in his 70's and he has CF! that's how I know I can make it with this disease! sure, i might have to have a lung transplant one day... but I make the best of my life! have any of you heard of the Sunny Shores Sea Camp???
1moe7 Says:
Dec 13, 2008 - same here man! i'm 13 and i have to go to thwe hospital every few months!!
BigAL0006 Says:
Dec 18, 2008 - My sisters boyfriend and probaly some day husband has cystic fibrosis. Hes actually one of the coolest guys ive ever met. All my sisters friends told her what if some something happens to him how are you going to deal with it. they told her not to date him cause it could be soo hard but she kept goin and stayed with him, i am so glad hes a part of my sisters life. and i hope he stays well for along time its such a scary diesease
vea210 Says:
Dec 22, 2008 - I was touched by this video. Love that song by Coldplay... "Fix you"
SarahJosine Says:
Jan 4, 2009 - I have cf, and I love this video. It's very sweet..
trinaababesx Says:
Jan 6, 2009 - A boy at my school had cf. unfortunately in 2008 he died at 16. so sadly it just shows not everyone makes it through this horrible disease.
kaleishot Says:
Jan 9, 2009 - Hey ya`ll im karson im 17 with cystic fybrosis ive acomplished somthing not many childeren with cystic fybrosis can do i have started bullring ive been riding for 3 years now and nothin is inpossible if you take care of yourself and put your mind to what you love to do
nikki135xx Says:
Oct 27, 2008 - thx,but it happens