We are looking for people with experience of children’s interstitial lung disease (chILD) from a range of countries in Europe to be part of a patient advisory group.
As part of this group, you would work with patient organisations, healthcare professionals and researchers to improve networking, information and research in this field.
You might be a parent of a child with ILD, or an adult with personal experience of ILD as a child, and be interested in being actively involved in representing the views of individuals with ILD at the European level.
If you, or someone you know, would like more information about this opportunity, please email Jeanette Boyd.
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