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We are asking parents, relatives and carers of children and young adults with bronchiectasis (aged under 18), and adults who were diagnosed with bronchiectasis as children, to tell us what we should be looking at to provide answers to the challenges of treating and looking after children with bronchiectasis.
What do YOU think needs to change or be considered to have the greatest impact on quality of life for yourself or your child with bronchiectasis?
This survey is part of the work of the European Lung Foundation and European Respiratory Society Paediatric Bronchiectasis Task Force to improve awareness and effective treatment of children with non-cystic fibrosis bronchiectasis. We want to improve the outcomes and lives of children with bronchiectasis and their parents/family.
This survey will take up to 15 minutes to complete, and is anonymous.