Learn why Emily Schaller participates in clinical trials to help advance treatments for cystic fibrosis.
Sarah Murnaghan, the 10-year-old girl at the heart of a US national debate over transplant lists, had successful lung surgery and is recovering well.
A hospital in Brazil came up with the idea of transforming the drugs and therapies of young cancer patients so they would feel like superheroes.
CF Europe is on Facebook! And as starting point we are celebrating the 36th European Cystic Fibrosis Conference. Join us!
After 32 years living with cystic fibrosis Sharon Brennan is now waiting for a double lung transplant. Here she explains her hopes and fears.
One Canadian living with cystic fibrosis and the challenges of her daily therapy.
The story of Catherine Kitz may not be a miracle, but it's close. The Montini senior distance runner was diagnosed with cystic fibrosis at 4 months old.
Travelling with cystic fibrosis: Recommendations for patients and care team members
Ethan lives with Cystic Fibrosis and this is his hospital experience from March/April 2013
'Somebody that I'll never know' is a short parody for organ donation awareness
You can have contact with other CFers if you follow some rules to avoid cross infection.
Good weather means fresh air and lot of events coming soon! Check them out!
40 women played the longest hockey game ever—243 hours worth in 10 days—to raise awareness and money for cystic fibrosis.
A young woman has found a novel way of beating cystic fibrosis - singing songs from the smash hit musical Les Miserables.
Vertex Begins Phase 3 Study of Kalydeco and VX-809. Targeting DF 508, the most Common CF Mutation.
Novartis TOBI Podhaler has obtained FDA approval for the treatment of bacterial lung infection in certain cystic fibrosis patients.
Why we’re here: CF Trust new film. We’re here to beat CF and make a daily difference to the lives of those with cystic fibrosis, and the people who care for them.
"This is my life and I fight hard every day against fate to change it.. I am mentally prepared to think that this is just a routine." También en español.
Dr. Dorota Sands has been treating people with cystic fibrosis (CF) for more than 20 years in her native country of Poland. También en español.
Studies have shown that patients with better forced expiratory volume tend to have a better health-related quality of life
Las Vegas event "Adding Tomorrows with Celine Dion" raises $1 million for CF Research. Also available in Spanish
The Boomer Esiason Foundation’s General Academic Scholarships assist CF patients pursuing undergraduate and graduate degrees
What is the daily routine of a CF patient? Questions and answers by a CF patient. Check out this video
The Italian CF Research Foundation funds research projects that have the ultimate aim to treat and eventually cure cystic fibrosis (CF).
Victory for Kalydeco Campaign in England
Introduction to Using TOBI Podhaler: Easy steps to take your TOBI Podhaler treatment on a proper way.
Kate (6 year old) is determined that her Cystic Fibrosis will not stop her dreaming big dreams.
CFFT will invest up to $58 million to speed the discovery and development of potential therapies
We have compiled some of the 2012 initiatives for you! Enjoy!
This video stars the team of the Belgian CF association ‘moving for air’!
Watch Jerry Cahill, 56 years old with CF and recipient of a double-lung transplant, on CBS's “Courage in Sports”.
Interview with Tamara del Corral, Physiotherapist and 2011 Young Investigators Award.
The family of a seriously ill Barnstaple teenager on a long waiting list for a double lung transplant.
"My transplanted organ is still working like Swiss clockwork" Lucas, CF patient. También en español.
NICE Approves Pharmaxis’ Bronchitol® As An Important New Treatment Option for Cystic Fibrosis Patients
‘Move For Air’ focuses on the importance of sport. This video wants to show that there are different ways of ‘moving’.
Lucas is a 29 years old CFer full of energy and with lot of experiences to be shared. También en español.
2012 North American Cystic Fibrosis Conference Kicks Off in Orlando with nearly 4,000 health-care professionals.
"As a business owner suffering from cystic fibrosis it’s no easy task combining it all" Steven De Wilder
From October to November 2012, CF Belgium organizes an awareness campaign inviting people to "Move For Air".
On October 18th and 19th CFE and CF Turkey organize the 3rd South Eastern European CF Conference in Istanbul, Turkey. Find the program and information on how to register.
Climbing for life - All 19 Asthma and CF patients made it to the top of the Galibier! Congrats to all of you and of course to all other participants, especially because the rain and the snow!
An Olympic windsurfer at the London Games is now trying to sell her medal to help a CF neighbor
U.S. Cystic Fibrosis Foundation updated their recommended guidelines of vitamin D
"Work Life and Cystic Fibrosis" by Dr. Dominique Hubert
Lindsay participated in the clinical trial of Kalydeco™. Then, dreams reborn again
For the first time, CF Worldwide will organize a Global awareness event
E.U has approved Kalydeco to treat people with CF
Study in the class of innovative therapies or CFTR correctors
Why females with cystic fibrosis do worse than males? Breakthrough Study
“Diagnose – to treat, treat – to?” 11th National Cystic Fibrosis Week (27 February – 04 March 2012)
World Spirometry Day 2012
3rd European CF Awareness week – 21-27 November 2011
34th European Cystic Fibrosis Conference: took place between June 8th and June 11th 2011 in Hamburg
