Our core content on Lung conditions and related factsheets has been translated to a number of other languages.
For more languages explore all available Factsheet translations.
Volunteer as a translator or learn how to translate using Chrome, Firefox or Edge browsers.
Our core content on Lung conditions and related factsheets has been translated to a number of other languages by our volunteer team.
For more languages explore all available Factsheet translations.
Volunteer as a translator or learn how to translate using Chrome, Firefox or Edge browsers.
Home » Patient representatives needed for two new Task Forces
If you have been affected by Pulmonary Alveolar Proteinosis (PAP) and/or pneumonia, you could help guide research by being part of a new Task Force.
A Task Force is a group of lung health experts working together to produce guidance on how to diagnose, treat, and manage different lung conditions and symptoms. Two new Task Forces are looking for patients to share their experiences and ensure that the guidance takes account of what is most important to patients.
For more information, or if you would like to get involved, please contact Clare: clare.williams@europeanlung.org
Sign up to get the latest information and research on lung conditions, hear about our upcoming events and campaigns, plus views from experts and patients! You can unsubscribe at any time.
ELF is a non-profit organisation registered as a UK company (VAT no. GB 115 0027 74) and charity (no. 1118930).
Our Brussels office enterprise number is 0738.383.695
European Lung Foundation's TR ID number in the Transparency Register is: 094039644810-79