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Welcome to the website of the European Pulmonary Fibrosis Federation

With 21 member organisations representing countries all over Europe, who unite their voices in the European organisation sharing experiences, sharing knowledge and communicating about PF care and treatment in the various countries the European Pulmonary Fibrosis Federation creates impact and influence on how the individual country handle the disease. We serve as the trusted resource for a united PF patient voice by raising awareness, providing disease education, advancing care, and funding research.

EU-IPFF brings together European national patient associations committed to defending their vision of equal access to treatment and care for all PF patients, regardless of geography, socio-economic status or age.