The Cystic Fibrosis Foundation has issued the following invitation to "Life Without Modulators Small Group Discussion." While many are celebrating the progression of CFTR modulators (Trikafta®, Symdeko®, Kalydeco® and Orkambi®), […]
The Cystic Fibrosis Foundation has shared the following announcement for an on-line discussion around body image.Adults with CF are invited to join an open conversation around body image. Based on BreatheCon 2024 feedback and community requests, the CF Foundation is offering a small group discussion where adults with CF can share experiences with each other […]
The invitation from the Cystic Fibrosis Foundation:You are invited to join the 6th annual ResearchCon on April 30-May 1, where you can interact virtually with researchers and clinicians and develop a deeper understanding of CF-related research and science topics. Past attendees have said that ResearchCon helps them better advocate for the changing health needs of […]
The invitation from the Cystic Fibrosis Foundation:You are invited to join the 6th annual ResearchCon on April 30-May 1, where you can interact virtually with researchers and clinicians and develop a deeper understanding of CF-related research and science topics. Past attendees have said that ResearchCon helps them better advocate for the changing health needs of […]
From the Cystic Fibrosis Foundation: Interested in learning about the latest cystic fibrosis research and care highlights from the North American Cystic Fibrosis Conference (NACFC)? Register for our live webinar November 12 at 7 p.m. ET to hear key takeaways from this year’s conference and have an opportunity to ask the experts your questions. REGISTER […]
The Cystic Fibrosis Foundation has extended the following invitation: Join us for an inspiring conversation with Michael Boyle, MD, President and CEO, and Irena Barisic, Executive VP and Chief Operating […]
From the Cystic Fibrosis Foundation: Whether you were diagnosed with cystic fibrosis at birth or recently received a diagnosis, there’s a spot for you at BreatheCon! This two-day virtual experience […]
From the Cystic Fibrosis Foundation: Whether you were diagnosed with cystic fibrosis at birth or recently received a diagnosis, there’s a spot for you at BreatheCon! This two-day virtual experience […]
Description from Cystic Fibrosis Foundation: This small group discussion is for adults with CF and offers a supportive environment to connect with others who share similar experiences. There is no […]
Here's the announcement from the Western New York Chapter of the Cystic Fibrosis Foundation: Celebrate the moment with us at the Western New York Chapter of the Cystic Fibrosis Foundation's […]
Description from Cystic Fibrosis Foundation: This small group discussion is for adults with CF 40+ and offers a supportive environment to connect with others who share similar experiences. Previous topic […]
The announcement from the Cystic Fibrosis Foundation: Join us at ResearchCon May 6! Everyone in the cystic fibrosis community is invited to this one-day, virtual event to discuss the latest […]