The Cystic Fibrosis Foundation supports universal masking in school to protect people with CF and other health conditions against COVID-19.
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The treatment has the potential to prevent Aspergillus fungal infections in people who have had a lung transplant.
Results show that people on Trikafta® enrolled in the six-week study were able to safely stop taking one of the two common CF medications without negatively affecting their health.
Bill will jump-start rebuilding of the antibiotics pipeline that is vital to stave off a looming pandemic.
More than 60 teens from across the country — 25 of whom live with cystic fibrosis — participated online and on Capitol Hill in the Foundation’s Teen Advocacy Day to advocate for the CF community.
Vertex’s copay assistance changes add an undue burden for people living with an already expensive, challenging lifelong disease.
The Foundation, in collaboration with external community advisors, finalizes recommendations in area of Community to help foster more inclusion and improve the experiences of Black people living with and impacted by cystic fibrosis.
The Board’s review put Coloradans with CF at the center of the discussion, helping to preserve vital access to Trikafta®.
Foundation welcomes new members to advance its mission
Clarametyx’s novel therapy aims to disrupt bacterial biofilms, one of the primary causes of antibiotic resistance, thereby potentially increasing the effectiveness of existing treatments in fighting a wide range of bacterial infections, including those commonly affecting people with CF.