by c4cfadmin | Jul 10, 2026 | News, Research
Cure4CF Update Team Ella driving hope for a future beyond CF Team Ella was created for one very special reason: Michelle and Shane’s daughter, Ella. At just eight years old, Ella lives with cystic fibrosis (CF), a lifelong condition that requires daily...
by c4cfadmin | Jun 26, 2026 | News, Research
Cure4CF Update Gut Instincts: Why Digestive Matters in Cystic Fibrosis Opinion piece by Professor Jodie Simpson I attended a really interesting scientific session at the European Cystic Fibrosis Society (ECFS) Conference in June 2026, and it started me thinking…. When...
by c4cfadmin | Jun 23, 2026 | News, Research
Cure4CF Update Cure4CF and Cystic Fibrosis Trust launch international research partnership to accelerate progress in cystic fibrosis Cure4 Cystic Fibrosis (Cure4CF) and Cystic Fibrosis Trust have announced a new Global CF Research Integration Grant, designed to...
by c4cfadmin | May 26, 2026 | News, Research
Cure4CF Update A Mother’s Instinct, A Life-changing Diagnosis In May 2014, Teresa and her husband Harry’s world changed overnight. Their first child, Simon, was 17 months old when he was finally diagnosed with cystic fibrosis (CF). Until that moment, they had never...
by c4cfadmin | May 21, 2026 | News, Research
Cure4CF Update CF Awareness Month Reflection: Why This Science Stays With Me Suzy Dimaline, CEO, Cure4CF To our incredible community, In our 20th year as Cure4CF, and during cystic fibrosis (CF) Awareness Month, I have found myself reflecting more than usual on the...
by c4cfadmin | May 11, 2026 | News, Research
Cure4CF Update A Decade of Change: How Bacteriophage Research Is Making a Difference for People with CF Professor Jodie Simpson, Head of Research, Cure4CF A decade ago, the idea of using bacteriophages—viruses that naturally kill bacteria—to treat chronic lung...
by c4cfadmin | Apr 27, 2026 | News
Cure4CF Update Running for Rory: A Mother’s Journey from Diagnosis to Determination Rory’s mum Miranda is lacing up her running shoes, she is not just training for a half marathon, she is running for Rory, his future, and a world without cystic fibrosis. Rory’s Auntie...
by c4cfadmin | Apr 24, 2026 | News
Cure4CF Update Running Together for a Cure: Taking on the Frontyard Ultra When this husband-and-wife duo lace up their running shoes, they’re not just chasing kilometres , they’re running for a cause, for community, and for a future without cystic fibrosis. Finding...
by c4cfadmin | Apr 24, 2026 | News, Research
Cure4CF Update From Defense to Damage: The Surprising Role of Mucus in Bronchiectasis Professor Jodie Simpson, Head of Research, Cure4CF What is mucus? Mucus is a protective, gel-like substance found throughout the body, where it traps germs, lubricates tissues, and...
by c4cfadmin | Feb 20, 2026 | News, Research
Cure4CF Update Understanding Pain in Cystic Fibrosis: Why it Matters Professor Jodie Simpson, Head of Research, Cure4CF Pain is a complex and deeply personal experience. It involves both physical sensations and emotional responses, acting as the body’s warning system...
Team Ella was created for one very special reason: Michelle and Shane's daughter, Ella. At just eight years old, Ella lives with cystic fibrosis (CF), a lifelong condition that requires daily treatments, ongoing medical care and extraordinary resilience.
Learn why digestive health is a vital but often overlooked part of cystic fibrosis (CF), and what the latest research reveals about gut symptoms and CFTR modulators.
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