Video duration: 397 seconds
Global video hits: 3601
My name is Katy and I am 23 years old. I just wanted to spread awareness about CF. Many people have heard of the disease but don't know exactly what it is about. Hoping that more awareness will lead to increased research and hopefully a cure in the near future!!
Video duration: 186 seconds
Global video hits: 7526
Cystic Fibrosis sucks. Kids find it tough to breathe and their lungs break down over time. There's no federal funding and no cure. Join the fight against CF and contribute to research to find a cure for this horrible disease.
Video duration: 267 seconds
Global video hits: 6203
Cystic fibrosis is the commonest inherited disorder in the UK. One in every 2,500 babies is born with cystic fibrosis. One in twenty-five people carry the defective recessive gene. It affects more than 7,500 babies, children and young adults in the UK. 14 year old Lauren Hutchins talks about living with the disorder.
Video duration: 375 seconds
Global video hits: 3078
Part 1 of a short film I put together this afternoon for Ms. Hall's biology 11 class. To give a little peak into the life of a double-lung transplant reciepient/ cystic fibrosis patient.
Video duration: 271 seconds
Global video hits: 2433
The Boomer Esiason Foundation for people who have Cystic Fibrosis is now in the world of Second Life. So those with CF can now interact with each other and outsiders with out having to wear mask or worry about getting sick. Goto Esiason.com for more information and updates, also how you can get involved
Video duration: 620 seconds
Global video hits: 3989
Hi, We just wanted to share some pictures of our sweet daughter Traci Ann Pelekoudas with this video. We lost Traci to Cystic Fibrosis on March 24, 2005. Tomorrow, Feb. 02, she would have been 20 years old. We miss her more than you can imagine.....
Video duration: 325 seconds
Global video hits: 4005
The Cystic Fibrosis Foundation is powered by the work of dedicated volunteers. Through their fundraising, CF patients are enjoying longer, healthier lives. But some CF patients are still dying before their time. This video, produced and directed by Dan Sonnett of the Sonnett Media Group, is a call to CF volunteers to strengthen their commitment to fight CF.
Video duration: 514 seconds
Global video hits: 4442
Part 2 of a short film I put together this afternoon for Ms. Hall's biology 11 class. To give a little peak into the life of a double-lung transplant reciepient/ cystic fibrosis patient.
Video duration: 495 seconds
Global video hits: 667
The Cystic Fibrosis Foundation strives to advance the search for a cure for CF by funding promising scientific research at medical centers and biotech companies nationwide. Frank Deford narrates this look at the Cystic Fibrosis Foundation's innovative approach to moving new treatments for CF into a pipeline that promises a better quality of life for all CF patients.
![Cystic Fibrosis Foundation: \"We Are Commitment\"](http://img.youtube.com/vi/ht3FxIg6k-M/2.jpg "Cystic Fibrosis Foundation: \\"We Are Commitment\\"")
![Cystic Fibrosis Foundation: \"Funding A Pipeline of Promise\"](http://img.youtube.com/vi/bpAYK-tumt8/2.jpg "Cystic Fibrosis Foundation: \\"Funding A Pipeline of Promise\\"")
