https://www.youtube.com/watch?v=485S0QC5ckE “Last year I went on a journey all over America while maintaining my Cystic Fibrosis care with new mobile medical devices. I am currently working on completely an in depth documentary about the challenges I faced, places I went and equipment I used on the trip.” Follow Beau Rich’s journey…
Image
Searching For Information On Pseudomonas Aeruginosa?
Searching for information on #PseudomonasAeruginosa? Read the most relevant articles here: https://bit.ly/1LiKW4E …
Furches Twins: Dealing with Cystic Fibrosis
Meet the 15 year-old Furches Twins, as they talk about their struggles dealing with Cystic Fibrosis. Ask questions and share your knowledge of Cystic Fibrosis in our forums. Follow her journey here: https://bit.ly/1VAjOnw…
According to the Cystic Fibrosis Trust, living with cystic fibrosis (CF) is a lifetime challenge that involves a strict, daily regimen of drugs, time-consuming physiotherapy and the risk of infection that can critically escalate at any time. In spite of the odds, singer and CF’er Bianca Nicholas is…
Clinical Trial FAQs – All You Need To Know
Check out the Frequently Asked Questions (FAQ) for clinical trials, and what the process involves. Read more here: https://bit.ly/1j4TxSt…
Everything You Need to Know About Orkambi
Orkambi is a combination therapy for treatment of cystic fibrosis. The FDA approval for the therapy was announced on July 2nd, 2015. Learn all about it here: https://bit.ly/1jCoQUT…
OneRepublic’s video begins with an intimate look into Warnecke’s daily treatment regimen for the disease, and is complemented by interview sequences where he outlines the history of his diagnosis, as well as the challenges and realities he faces both now and in the future. Continue reading: https://bit.ly/1PQSZtO…
#tbt – Remembering Jennifer
Remembering Jennifer’s story, the amazing woman who, unfortunately, lost the battle against Cystic Fibrosis after 23 years of fighting. Read the full article here: https://bit.ly/1jAqRRu…
Gifted Life is committed to support and nurture transplant recipients, their family and friends and to promote organ donation and has recently posted this video about what not to say to someone living with a chronic illness such as cystic fibrosis. Learn more about CF.
Your CF Community

Visit the Cystic Fibrosis News Today forums to connect with others in the CF community.
Recent Posts
- New CFTR panel expands detection of cystic fibrosis gene variants
- Sharing about my CF diagnosis helped me find my village
- American Airlines ski event raises more than $1.6M for CF Foundation
- Spring has sprung: Reflections on the beauty of post-transplant life
- Advocacy has a way of bringing out the best in people