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Every Breath Counts

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Canadian Cystic Fibrosis Foundation video spreading awareness about CF

Channel: People & Blogs
Uploaded: November 30, 1999 at 12:00 am
Author: CCFFadmin

Length: 10:42
Rating: 4.83
Views: 17136

Tags: Breath  Counts  Cystic  Every  Fibrosis  

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Video Comments

54spiritedwill54 (November 30, 1999 at 12:00 am)
My daughter has CF, this is a very important subject for me. I prey every day for a cure.
xshexyxox (November 30, 1999 at 12:00 am)
Hi.My best friend has just died aged 14 yrs of age.He spent 9 months a yr in hospital since he was 2.He needed a heart and a lung transplant.If anyone here is living in ireland please fundraise or give money 2 help build a foundation in ireland there is not 1.the population is so small that there is not many matches.Please help and donate or fundraise. thankyou. great video. God bless everyone with cf!
SeksiKitty (November 30, 1999 at 12:00 am)
The CCFF did agreat job with this info video.I had a daughter Sarah with CF who passed away in July 2006. Sarah had just turned 20 6 weeks before. I miss my girl dearly,she was my only child. To help I now do the Great Strides walk Sarah began in 2005 in memory of her best friend Rachel who had CF too. A few of us got a team together,we call it "Angels of Hope".Each year I'm walking in memory of those we have lost to CF. Lets all pitch in & make CF stand for Cure Found!
GOBBYBITCH2K8 (November 30, 1999 at 12:00 am)
n i had to fuckin watch this at skwl in sceince
GOBBYBITCH2K8 (November 30, 1999 at 12:00 am)
wot the fuck wit ur comment on ma pageeesmegg eddtap bak batty man x
teiubesc36 (November 30, 1999 at 12:00 am)
just pray that is found a cure very soon,so that way,CF won,t take those we love so much,my heart is with you all,never give up fighting,never loose hope please,even if some days you don,t have the strenght to do it,god bless you all,and a big thanks to this foundations and volunteers who help and do everything they can...good bless
teiubesc36 (November 30, 1999 at 12:00 am)
i found out about this desease,about one year ago,when a singer that i admire a lot pass away from it,he was 23 years old,i start to learn more about CF,i don,t have it,but my heart is with everyone who does,i
missdrpc (November 30, 1999 at 12:00 am)
hi! im gunna do a fundraiser in my town! i really wanna help out and find a cure, i dont have cf but my brother did he died a year and a half ago, thanks for posting the video
sylvainlarue (November 30, 1999 at 12:00 am)
one of my bestfriends has CF. she always has to miss special ocasions and hang outs cause of it. though she still lives a normal life, it sometime really affects her :'(
xBlackFallenAngelx (November 30, 1999 at 12:00 am)
Wow..after looking at this video, I was surprised at how many people have CF. I was browsing through YouTube because I was studying for a Science test about Cystic Fibrosis. Even though I dont have CF, I am really touched at how much confidence the people have. I hope that IF I do have CF, i would be the same.

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