
Raise awareness
Download and share our promotional pack of social media posts, tiles and newsletter content using #PFAwarenessMonth and #PFHeroForHope. Together, we can change lives and provide hope for a brighter future.
Share your story
Help us give hope and inspiration to the individuals and families affected by pulmonary fibrosis by sharing the story of how you or someone you love has been affected by the disease and what research means to you.
PF Heroes for Hope
Bill
Bill was diagnosed with Idiopathic Pulmonary Fibrosis in 2015 and has been championing awareness and funding for improved access to care and research through a number of awe inspiring fundraising efforts.
Linda
After experiencing a persistent cough for years, Linda was eventually diagnosed with Idiopathic Pulmonary Fibrosis. Since her diagnosis she has dedicated her time to supporting others living with Pulmonary Fibrosis through our Peer Connect Service.
Tamera
Associate Professor Tamera Corte, is a Consultant Respiratory Physician. Tamera is a Chief Investigator of the Centre of Excellence in Pulmonary Fibrosis (CRE-PF). Through our multi-million-dollar research program, Lung Foundation Australia and CRE-PF are partnering to drive discoveries in PF.
Dan
Professor Dan Chambers is a Thoracic and Transplant Physician with long-standing clinical and research interests in lung fibrosis. Dan is Chair of Pulmonary Fibrosis Australasian Clinical Trials Network.
Laura
Dr Laura Glenn is a final year Advanced Trainee in Respiratory Medicine and was the 2019 recipient of the Di Cox PhD Scholarship in Idiopathic Pulmonary Fibrosis Research. With this funding Laura is hoping to improve diagnostic pathways for patients.
Philippa
As a wife of someone living with PF, Philippa is determined to help raise awareness of this devastating disease and help provide hope for a brighter future. This October, Philippa will be fundraising to raise vital funds to support life-changing research.
Pulmonary Fibrosis Fact Sheets
In collaboration with the Centre of Research Excellence in Pulmonary Fibrosis, Lung Foundation Australia developed four free and downloadable fact sheets for people living with Idiopathic Pulmonary Fibrosis (IPF).
Peer Connect
Peer Connect is a peer to peer matching program which connects people with a similar lived experience of lung disease. Peer connect provides the opportunity for two people to share their experiences with someone who ‘gets it,’ providing each other with a listening ear and encouragement.
Educational Webinars
Hear information, advice and support on living with Idiopathic Pulmonary Fibrosis (IPF) from experienced health professionals as well as patients. You can join the webinar live from the comfort of your own home or access a recording after the event.
Life With Pulmonary Fibrosis
Download a free copy of the Life with Pulmonary Fibrosis ebook to learn more about managing your condition. This resource was developed in collaboration with leading healthcare professionals.