by Oliver Prenton | Apr 20, 2020 | News
Lachie Monfries Takes Over Cure4CF Lachie Monfries I’m a 35-year-old with cystic fibrosis, I am married and have a cheeky 6-year-old boy Harvey, I’m proud to be deputy chair for Cure 4 Cystic Fibrosis and am passionate about the work we do to fund world leading...
by c4cfadmin | Nov 13, 2019 | News
Major Research Announcement. Successful Recipient – Barbara Stow-Smith Cystic Fibrosis Innovation Grant. We are thrilled to welcome Professor Marc Pellegrini to our Cure4 Cystic Fibrosis Army as the first successful grant recipient of our inaugural National...
by Suzy Dimaline | May 27, 2019 | News
CMV Group Foundation We welcome the CMV Group Foundation to our CF Army We are thrilled to announce the CMV Group Foundation as Naming right sponsor of our inaugural Community Ambassador Program. Through this innovative program we will recruit local, passionate and...
by Suzy Dimaline | Apr 29, 2019 | News
Phage Therapy update We spoke with Sarah Vreugde, Senior Scientist from the ENT Research Group at the Basil Hetzel Institute in Adelaide, who is currently working on the Phage Therapy project. We asked Sarah how the project was progressing and were thrilled to hear...
by Suzy Dimaline | Apr 29, 2019 | News
Meet In Celebration fundraiser, Michelle This month we spoke to Michelle about what it’s like to fundraise for Cure4CF as part of her birthday celebrations. You chose to support Cure4CF recently in lieu of gifts for your birthday celebrations, with many...
by c4cfadmin | Nov 1, 2018 | News
I Have 65 Roses Meet first time author, Holly who has written and illustrated her own book inspired by her cousin who has cystic fibrosis (CF). Holly is donating all profits from her book sales to Cure4CF. Read more about how you can get involved below. “As a...
by c4cfadmin | Nov 1, 2018 | News
Introducing new Chair Jo Close Cure4CF is proud to introduce Ms Jo Close as the new Chair of the Foundation. Jo was appointed to the board of Cure4 Cystic Fibrosis Foundation in December 2013 and has been an active contributor to the development of the organisation’s...
by c4cfadmin | Nov 1, 2018 | News
Meet Fight Squad Member, Danyelle This month we spoke to Danyelle about what it’s like to be a part of CF Fight Squad. How do you currently support the work of Cure4CF? I am a member of the CF Fight Squad by making a monthly direct debt donation. You’ve been a...
by c4cfadmin | Nov 1, 2018 | News
Gandel Philanthropy Gandel Philanthropy recently awarded Cure4 Cystic Fibrosis $167,000 to fund the appointment of an X-Ray Lung Functioning Imaging Analyst based at Monash University and the Australian Synchrotron. Dr Freda Werdinger has been appointed to the...
by c4cfadmin | Oct 23, 2018 | News
Phage Therapy Funded by C4CF, CFSA and The Hospital Research Foundation, the Adelaide ENT Research group at the Basil Hetzel Institute are aiming to eliminate drug resistant bacteria in CF using bacteriophage. Bacteriophage is a virus that can eliminate very specific...
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?
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 fibrosis (CF) community.
Recent Comments