CF-Cystic Fibrosis-Awareness:Every Breath Counts
I know there are many other info vidz on Cystic fibrosis but i thought it was about time 4 a updated vid.This is an information video to bring cystic fibrosis:a genetically inherited & life-threatening condition, into the spotlight.CF is a common condition which need the help and support of everyone to fight against CF. At this moment in time,there is no cure for cystic fibrosis but we hope 2 find it one day with your help.Plz pass this video on to everyone you know;the more ppl that are aware of CF,the quicker we can get to finding that cure,plz help us see off CF.thank you. [sufferer of CF]
Tagged with: Cf • Cystic Fibrosis • Vidz
Filed under: Cystic Fibrosis
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Thanks. A friend who has a loved one with CF passed this on to me. Very good video. Here’s hoping for a cure soon.
really all u do is take your medicines, live a normal life, and stuff. the best thing u can do is not to tell her to cover her mouth if she doesnt or not to tell her stop caughing or something. really just ignore all the caughing, becuase cf patients are already very self consious, the best thing to do is not to make them more self concious
hi, my name is kayla, im 14 and i advise you DONT do it. i used to not do my treatments and i went to the hospital 5 times that year, after being out for 3 years. i sometimes cut it short but i dont just NOT do it. please, dont end up like that or worse.
Kayla
Every time i watch this video it brings so many emotions up its that fantastic!! I have spread it across face book to all my friends on there to promote the understanding of CF!!
Thankyou again for making it!!
Keep up the fight x
Hi I am 15 and get sick of my treatment so much so I just
don’t do it . Got any advice . Good for u that u do it
if you guys have a chance my cousin started a page on facebook he is putting his battle against cf for the world to see and help others undrerstand and give supoort to others and their families it is 365 breaths by eric hintz i encourage u to look it up well worth it and u can share your stories as well
This video is wonderful!!
Thankyou for making it!!
I have been affected by CF my best friend who sadly passed away on 24th april 2001 aged 16, had CF an if we can make the world aware of CF and what it is, then we can help those diagnosed in th future!!
Spreading the word about CF can help rase awareness which i turn can help the CF trust find a cure one day!! Well thats my dream any how!! Even if i’m not here to see them find that cure I know by spreading the word I have helped in some way!!
I have cystic fibrosis. i am 13. my friend heather died this may due to cystic fibrosis. she was 18. thakns so much for making this video. i will pass it on
let us fight CF!
good vid
so can someone plz tell me how do u fight it [[ i dont have it, im 14]] but a friend of mine was diagnozed with it so im gonna try to help her
thnx for making the vid 5*s
vicky wright died january this year x
god bless u marissa x
My best friend was digonsed with cistic fibrosis
RIP
Alex, Phillip, & Shamberly
I am 16 years old,
and i have Cystic Fibrosis!
I was diagnosed December 10 1992
6 months exactly after i was born.
♥Marissa♥
i got diagnosed when i was only a day old after an operation … my best friend also died when she was just 14 i am now 16 and i have been keepin great xx a luv this video :d xxx
sorry, 1:20
i know th girl at 1:14 (vicky), shes my cousins cousin
it is important that people know about cystic fibrosis, my sister lived with it 4 17 years and sadly lost her life after a transplant. i like the video. xxxx
Oh my god! How’d you get that photo at 1:24? Thats my sister shelley white and my dad Jim white!
I am 15 and they caught mine at 4 years ago
….
This is a beautiful video. I live with CF also, so it touched me on a personal level. Great way to spread awarness and express what we really go through!
Breathe and Believe!
Greatt Viideo
=]
i’m 14 now but I was diagnosed @ 2 weeks old…. But that is because I was in distress in inside so they took tests straight away…. I’ve heard recently they can now diagnose it within 48 hours!
I have CF and I tried making my own video like this it was great but it was de wrong format for youtube ….. can anyone help me convert it to the right format? Please?!
BTW brill video….
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