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European Lung Foundation
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.
We are delighted to launch our new LAM website, developed with the support of women with lymphangioleiomyomatosis (LAM) and healthcare experts working in the field, at the start of Worldwide LAM Awareness Month (June 2017).
LAM is a rare lung condition that mainly affects women. To find out more, download our factsheet (in 9 languages) and access our map of LAM patient support organisations on the in your language page.
Find out what matters most to women diagnosed with LAM and read stories of the experiences of women diagnosed with this condition.
Please pass on details of the website through your networks to help spread awareness of this rare lung condition; and let us have your feedback.
We also want to acknowledge and thank the women of our LAM patient advisory group who helped guide the development of this project.
Visit the LAM patient priorities website.
Visit the patient priorities homepage to see which websites will be coming next.
Sign up to our free monthly newsletter to get the latest information and research news on lung conditions, 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