Connecting with others
Talking to someone who really gets what you’re going through can make a big difference. Our PF and ILD Peer Connect service can match you with someone else who is going through a similar situation. We’ll help you connect over the phone so you can share and support each other.
Resources
A diagnosis of pulmonary fibrosis can feel isolating, but you’re not alone. Lung Foundation Australia, in partnership with the Centre of Research Excellence in Pulmonary Fibrosis, are here to provide you with the tools and information you need to live well with your condition. Explore the resource hub to access evidence-based resources on a range of topics including symptom management, medications and getting the most out of your treatment and care.
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Support groups
Support groups are a safe and friendly place where people with similar experiences can get together face-to-face or online. You can support each other, share tips and feel less alone. Lung Foundation Australia can help to find a group near you.
Webinars
Learn more about your condition from health experts and people living with PF. Our webinars are a great way to get the latest info, advice, and support. You can watch live from home or catch a recording later.
Pulmonary rehabilitation
This is an exercise and education program run by specially trained health professionals. They will teach you how to manage shortness of breath and stay well.
Lungs in Action
After pulmonary rehabilitation, it’s important to keep exercising to stay fit. The Lungs in Action program is a fun exercise class to help people with lung disease or lung cancer maintain the benefits from pulmonary rehabilitation and live their best life. Learn more, or let us know if you’re interested in a class.
Support and palliative care
Palliative care can be a great help for you and your family. It’s all about improving your quality of life so you can live as well as you can for as long as possible. It works along with your other treatments and helps you manage your symptoms.
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