EU-PFF set up 2 years ago a Pulmonary Fibrosis Community Advisory Board (PF-CAB) as a working...

The European Pulmonary Fibrosis Federation (EU-PFF) is pleased to announce the appointment of John...

The 6th session of a new series of monthly and free webinars for the Pulmonary Fibrosis community...

The 6th session of a new series of monthly and free webinars for the pulmonary fibrosis community...

The fifth session of a new series of monthly and free webinars for the Pulmonary Fibrosis...

Would you like to know which projects we have initiated, implemented and continued in 2023 and...

What can PF patients do to improve their mental health? This and other questions will be addressed by Prof Brendan Kelly, Professor of Psychiatry at Trinity College Dublin and Consultant Psychiatrist at Tallaght University Hospital, Dublin, in the upcoming session on “Living with Lung Fibrosis: Optimising Mental Health and Wellbeing”. The session will be moderated by Liam Galvin, EU-PFF CEO.

Dear EU-PFF Community,  As the year draws to a close, you will find all the EU-PFF projects,...

Together with the European Lung Foundation (ELF), EU-PFF has developed a guide for pulmonary fibrosis patients and their carers. In its 24 pages and 8 chapters, “Pulmonary Fibrosis: a supportive guide” covers essential aspects such as the disease itself, treatment, supportive care and living well.

The 2023 EU-PFF BreathingLife Campaign Report (Pulmonary Fibrosis Awareness Month & IPF...

Our adherence survey is still running until November 30th. The survey is aimed exclusively at...

The fourth session of a new series of monthly and free webinars for the Pulmonary Fibrosis...

The 4th session of a new series of monthly and free webinars for the pulmonary fibrosis community...

The third webinar of a new series of monthly and free webinars for the Pulmonary Fibrosis...

The third session of a new series of monthly and free webinars for the pulmonary fibrosis...

The Imperial College London is running a qualitative research project (meaning there are no...

In the past few months, the Federation has been working on a survey to assess the extent to which pulmonary fibrosis patients adhere to their medications. In order for this survey to yield meaningful results and contribute to better health care for PF patients, we would like to ask you for your help and 20 minutes of your time.

Today kicks off Pulmonary Fibrosis Awareness Month! It takes place every September and aims to raise awareness about Pulmonary Fibrosis, its challenges and the changes it brings to daily life, as well as the burden it places on patients and their loved ones

A lot has happened in the field of Pulmonary Fibrosis in the time since our last newsletter in...