Cystic Fibrosis Videos

Cystic Fibrosis Video

Cystic Fibrosis
Sep 01, 2010
10 minute documentary final project about a day in the life of a ten year old girl with Cystic Fibrosis

Watch Current TV presents 'Dying Young' Video

Current TV presents 'Dying Young'
Sep 01, 2010
This documentary short explores the struggles of living with cystic fibrosis. Produced by and for Current TV.

What is Cystic Fibrosis?
Sep 01, 2010
A short film on the what cystic fibrosis does to the body.

Cystic Fibrosis
Aug 29, 2010
this is a nice little video that a friend put together as a personal project because his daughter has CF.

Cystic Fibrosis Emcee: VC2
Aug 27, 2010
Citizen Aim is a 27 year old emcee in Yuma, Arizona who might literally rap his last breath. That's because he's expected to die from Cystic Fibrosis by age 35. Diagnosed with the fatal chronic illness as an infant, Citizen Aim is amongst the 70000 people worldwide living with this death sentence sometimes referred to as '65 Roses. In this pod, by vc2 producer Carlos Aguilar, Citizen Aim talks about his disease, his treatment, and how his recovery themed songs are an inspiration others suffering from the disease.

Watch UltraViolet: Cystic Fibrosis Foundation Video Video

UltraViolet: Cystic Fibrosis Foundation Video
Sep 03, 2010
We raise money for the Cystic Fibrosis Foundation to help Violet and everyone else find a cure for this disease. please donate safely and securely online at: www.cff.org/Great_Strides/RebeccaDixon5175 www.cff.org www.myspace.com/ultraviolet_rockforcf

Living with Cystic Fibrosis
Sep 02, 2010
Living with Cystic Fibrosis.

Cystic Fibrosis
Aug 27, 2010
Learn more about the #1 genetic killer of children and young adults in the United States, Cystic Fibrosis, and what you can do to help!

Cystic Fibrosis - My Story
Aug 27, 2010
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!!

Cystic Fibrosis and Me
Aug 27, 2010
I walk you through my treatment routine.

Luminex Announces Commercial Launch of New Cystic Fibrosis Test
AUSTIN, Texas, Aug. 26 /PRNewswire-FirstCall/ -- Luminex Corporation (Nasdaq: LMNX), the worldwide leader in multiplexed solutions, today announced the full commercial launch of its xTAG® Cystic Fibrosis 60 Kit v2, a new diagnostic test that can simultaneously screen a single blood sample for up to 60 cystic fibrosis-causing genetic mutations in a matter of hours.

'Improving Access to Clinical Trials Act' Passes U.S. Senate in Victory for CF Advocates
BETHESDA, Md., Aug. 6 /PRNewswire-USNewswire/ -- The U.S. Senate last night passed the "Improving Access to Clinical Trials Act" (I-ACT), a bipartisan piece of legislation championed by the Cystic Fibrosis Foundation, its advocates and 120 other health advocacy organizations.

Fifth Annual Hook the Cure Fishing Tournament Set for October to Benefit Cystic Fibrosis Foundation
The IGFA-qualifying tournament is expected to attract more than 120 for the competition and the accompanying golf and spa packages. $1.3 million NET generated since inception of event.


	Cystic Fibrosis Treatments

	Home - Site Map - Featured: Cystic Fibrosis Video Cystic Fibrosis Videos Cystic Fibrosis Video Cystic Fibrosis Sep 01, 2010 10 minute documentary final project about a day in the life of a ten year old girl with Cystic Fibrosis Current TV presents 'Dying Young' Sep 01, 2010 This documentary short explores the struggles of living with cystic fibrosis. Produced by and for Current TV. What is Cystic Fibrosis? Sep 01, 2010 A short film on the what cystic fibrosis does to the body. Cystic Fibrosis Aug 29, 2010 this is a nice little video that a friend put together as a personal project because his daughter has CF. Cystic Fibrosis Emcee: VC2 Aug 27, 2010 Citizen Aim is a 27 year old emcee in Yuma, Arizona who might literally rap his last breath. That's because he's expected to die from Cystic Fibrosis by age 35. Diagnosed with the fatal chronic illness as an infant, Citizen Aim is amongst the 70000 people worldwide living with this death sentence sometimes referred to as '65 Roses. In this pod, by vc2 producer Carlos Aguilar, Citizen Aim talks about his disease, his treatment, and how his recovery themed songs are an inspiration others suffering from the disease. UltraViolet: Cystic Fibrosis Foundation Video Sep 03, 2010 We raise money for the Cystic Fibrosis Foundation to help Violet and everyone else find a cure for this disease. please donate safely and securely online at: www.cff.org/Great_Strides/RebeccaDixon5175 www.cff.org www.myspace.com/ultraviolet_rockforcf Living with Cystic Fibrosis Sep 02, 2010 Living with Cystic Fibrosis. Cystic Fibrosis Aug 27, 2010 Learn more about the #1 genetic killer of children and young adults in the United States, Cystic Fibrosis, and what you can do to help! Cystic Fibrosis - My Story Aug 27, 2010 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!! Cystic Fibrosis and Me Aug 27, 2010 I walk you through my treatment routine. Luminex Announces Commercial Launch of New Cystic Fibrosis Test AUSTIN, Texas, Aug. 26 /PRNewswire-FirstCall/ -- Luminex Corporation (Nasdaq: LMNX), the worldwide leader in multiplexed solutions, today announced the full commercial launch of its xTAG® Cystic Fibrosis 60 Kit v2, a new diagnostic test that can simultaneously screen a single blood sample for up to 60 cystic fibrosis-causing genetic mutations in a matter of hours. 'Improving Access to Clinical Trials Act' Passes U.S. Senate in Victory for CF Advocates BETHESDA, Md., Aug. 6 /PRNewswire-USNewswire/ -- The U.S. Senate last night passed the "Improving Access to Clinical Trials Act" (I-ACT), a bipartisan piece of legislation championed by the Cystic Fibrosis Foundation, its advocates and 120 other health advocacy organizations. Fifth Annual Hook the Cure Fishing Tournament Set for October to Benefit Cystic Fibrosis Foundation The IGFA-qualifying tournament is expected to attract more than 120 for the competition and the accompanying golf and spa packages. $1.3 million NET generated since inception of event. Shoppers get steamy for cystic fibrosis Denny Hamlin Foundation donates $10,000 for life-saving transplant Cyclist's hard work pays off for charity Vital Signs: New drugs for cystic fibrosis bring hope Name change reaches to past		ARIKACEâ„¢ Demonstrates Sustained Benefit in the Treatment of Cystic Fibrosis Patients Who Have Pseudomonas Lung Infections MONMOUTH JUNCTION, N.J., June 17 /PRNewswire/ -- Transave, Inc., today reported interim results from a multi-cycle Phase II open label clinical trial in cystic fibrosis (CF) patients on its lead investigational drug, ARIKACEâ„¢ (liposomal amikacin for inhalation). US Cystic Fibrosis Market to Exceed $896 Million by 2015, According to New Report by Global Industry Analysts, Inc. GIA announces the release of a strategic report on Cystic Fibrosis market in the US. The US market for cystic fibrosis (CF) is projected to exceed $896 million by 2015. Largely driven by the sales of two leading drugs, Pulmozyme and TOBI, the market is expected to further expand significantly over the coming years, given the successful launch of novel and enhanced drug formulations or therapies including new mucolytic drugs, pancreatic enzyme replacement drugs, anti-inflammatory drugs, and drugs targeting genetic CFTR defects. 'Improving Access to Clinical Trials Act' Passes U.S. Senate in Victory for CF Advocates BETHESDA, Md., Aug. 6 /PRNewswire-USNewswire/ -- The U.S. Senate last night passed the "Improving Access to Clinical Trials Act" (I-ACT), a bipartisan piece of legislation championed by the Cystic Fibrosis Foundation, its advocates and 120 other health advocacy organizations. Hope for Cystic Fibrosis Sufferers An inherited disease, cystic fibrosis is thought to affect about 30,000 Americans and is the most common, life-shortening genetic disease known. Much of the population has heard the term cystic fibrosis, but few understand its meaning or consequences. Subscribe to our Monthly Email Newsletter