From November 3rd-5th 2022, the second virtual European Pulmonary Fibrosis Patient Summit brought together patients and caregivers, healthcare professionals, policy makers and industry representatives, with 12 Sessions and 37 speakerscovering a wide range of topics including clinical, treatment, patient involvement and research. You can find the report here.
“Pulmonary Fibrosis: a supportive guide” – a joint project by the ELF and EU-PFF
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.
