by c4cfadmin | Nov 27, 2025 | News, Research
Cure4CF Update Why D-Day Matters: Sophia’s Story As D-Day approaches, we spoke with Cure4CF supporter and advocate Sophia Leopardi about her family’s journey with cystic fibrosis, the power of research, and why this day of giving has become so important to her,...
by c4cfadmin | Nov 20, 2025 | News, Research
Cure4CF Update Driving Innovation: More Than $1 Million Awarded to Advance CF Research Cure4 Cystic Fibrosis Foundation (Cure4CF) has today announced four new research projects that will receive funding through its Holckner Family CF Impact Grant with over one million...
by c4cfadmin | Nov 10, 2025 | News, Research
Cure4CF Update Thinking About Joining a Clinical Trial? Here’s What You Should Know Professor Jodie Simpson, Head of Research, Cure4CF I was recently invited to take part in a clinical trial, and it made me stop and think about how many people might not really know...
by c4cfadmin | Oct 13, 2025 | News, Research
Cure4CF Update Cure4CF and Lung Foundation Australia unite to strengthen bronchiectasis research Cure4CF is proud to join forces with Lung Foundation Australia (LFA) to strengthen research into bronchiectasis – a chronic lung disease that affects many in our cystic...
by c4cfadmin | Sep 12, 2025 | News, Research
Cure4CF Update Rare Genetic Mutations in Cystic Fibrosis – Why They Matter More Than You Think Professor Jodie Simpson, Head of Research, Cure4CF Cystic fibrosis (CF) is what’s called an autosomal recessive condition. That means a person needs to inherit two faulty...
by c4cfadmin | Aug 15, 2025 | News, Research
Cure4CF Update Spit Happens. From Phlegm to Facts: Understanding Wet Coughs Professor Jodie Simpson, Head of Research, Cure4CF Let’s talk about something we don’t often discuss openly—sputum. You might know it better as phlegm or mucus, and if you’ve ever had a wet...
by c4cfadmin | Aug 14, 2025 | Events, News
Cure4CF Update Running for Breath: Kyle’s Journey from CF Diagnosis to Ultra Marathons When Kyle laces up his running shoes, he is not just preparing for another training session, he is fighting for his health, his future, and the dream of a world without cystic...
by c4cfadmin | Jul 25, 2025 | News
Cure4CF Update Reflections from the 48th European Cystic Fibrosis Conference Professor Jodie Simpson, Head of Research, Cure4CF In June 2025, Milan played host to the 48th European Cystic Fibrosis Conference (ECFS), drawing together the brightest minds in cystic...
by c4cfadmin | Mar 11, 2025 | News, Research
Researcher Spotlight From Mumbai to Brisbane and Liver to Lungs: How Dr Divya Ramnath is tackling inflammation and infection in Cystic Fibrosis. Last month I had the chance to speak with Dr Divya Ramnath, one of the team working on the Think Zinc program this year....
by c4cfadmin | Feb 12, 2025 | News
Cure4CF Update “The number” – the changing landscape of lung function testing in cystic fibrosis When we visited the Mater in Brisbane last year as part of our tour with Dr Lucy Burr we visited the lung function laboratory. Here we met Respiratory Scientist Grace...
I was recently invited to take part in a clinical trial, and it made me stop and think about how many people might not really know what that means. Clinical trials are often mentioned in the news or by health professionals, but what happens in one—and why do people volunteer?
I was recently invited to take part in a clinical trial, and it made me stop and think about how many people might not really know what that means. Clinical trials are often mentioned in the news or by health professionals, but what happens in one—and why do people volunteer?
Recent Comments