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.
We are delighted to launch a new website that provides information about children’s interstitial lung disease (chILD) for parents and caregivers of infants, children and teenagers living with the condition across Europe.
The website was produced as part of our patient priorities projects. We developed it with the support of parents and caregivers of infants, children and teenagers living with these very rare lung conditions and healthcare experts in the field who are members of the ChildEU Clinical Research Collaboration (CRC) which promotes awareness and research into chILD. Our thanks to everyone involved for their sharing their experiences and expertise.
We encourage you to visit the website and find out more about diagnosis, treatment and the experiences of parents and their children, and pass it on through your networks to help spread awareness.
We will add more information to the website in a range of languages over the next few months and look forward to receiving your feedback.
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