Profile
Name:
Cystic Fibrosis Foundation
Channel Views:
65,791
Total Upload Views:
653,511
Age:
57
Joined:
Jul 13, 2007
Latest Activity:
1 week ago
Subscribers:
1,292
Website:
Cystic fibrosis is a life-threatening genetic disease that affects the lungs and digestive systems of approximately 30,000 children and adults in the U.S.
More than 10 million Americans are symptomless carriers of the defective CF gene.
The Cystic Fibrosis Foundation is the leading organization committed to finding new therapies and ultimately a cure for CF.
Help fight CF! Visit www.cff.org to learn more.
More than 10 million Americans are symptomless carriers of the defective CF gene.
The Cystic Fibrosis Foundation is the leading organization committed to finding new therapies and ultimately a cure for CF.
Help fight CF! Visit www.cff.org to learn more.
Country:
United States
Subscribers
(1292)
Channel Comments
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Mtpest01
(1 month ago)
wuwuw, so painful to watch these patients!!
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Hockeyjeph88
(3 months ago)
Hey Guys. My name is Jeph and I'm a 14 year old with CF. It freaking sucks, but there is hope. I'm trying to get teens with CF talking, so check it out please? It would mean a lot! :) my facebook page- search Cystic Fibrosis Teen Chat i dont have any followers so it would help a lot to like it! and my website is posted on there, Youtube isn't letting me put it on here.. thanks so much! Also, if you would like to message me, feel free to do so, i check my fb and youtube every day :) God Bless"
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gg3bones
(3 months ago)
i have cf and i can rap check my videos out the one that says keep your head up its about cf and how it all made life hard maybe send this to cf foundation it would be awsome thanks CURE FOR CF PLEASE GOD
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alonzo12357
(6 months ago)
my son has cf his name is alonzo peterkin
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ledfootbabe
(6 months ago)
My best friend who now is 31 almost 32 yrs old has CF...I pray each day that a cure will be found. I also pray each day that he will wake up and live....
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zackyv08
(7 months ago)
Heya, im a person from ireland with CF and were doing a facebook event to raise awarness of Cystic Fibrosis and also to get a Guinness World Record, if ye all could join and spread the word it would be great. just type into facebook "make cystic fibrosis aware by trying to break a world record". All support would be very greatful
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pupydejz
(7 months ago)
Hello everyone.
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redrabbitfilms
(10 months ago)
Hey everybody. I'm try to help raise awareness through a youtube contest. Our oldest has CF and I made a film about it. Please check out my video and vote. CF = Cure Found
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RGreen6732
(10 months ago)
The Co-CEO of BJ's Restaurants has a daughter that has CF and created a program called Cookies for Kids. Every time you order a Pizookie at their restaurant, a portion of the sales goes to the CFF Foundation to help find a cure for this disease.. Please pass the word around...
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RGreen6732
(10 months ago)
I have the gene but its not active in me. I had 2 brothers who passed recently. My older brother was 42 when he passed (May 2006). He was able to have a dual lung transplant which gave him an extra 6.5 years. My younger brother passed at 35 1/2 (Dec 2009). He wasn't able to have a lung transplant because he also had another bacteria called Cepacia. He was not allowed to be put on the lung transplant list. I also have 2 nephews who currently have CF as well... I'm very familiar with this disease... I hope one day there is a cure for this disease... God has bless me with the time I was able to have with them...
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