Influence childhood bronchiectasis research and treatment by sharing your experiences in a new survey
ELF has launched a survey to learn more about the impact of bronchiectasis on children and young adults.
The survey is open to:
- Parents, relatives or carers of children or young adults with bronchiectasis
- Adults who were diagnosed with bronchiectasis as children
Your anonymous responses will help healthcare professionals and researchers understand more about the challenges of treating and looking after children with bronchiectasis.
The survey is available in 9 languages: English, French, German, Greek, Italian, Polish, Portuguese, Spanish and Russian.
Help us reach as many people as possible by forwarding the survey link below to anyone who may be interested in sharing their views.
If you have any questions, please email firstname.lastname@example.org
This survey was developed by ELF and the ERS Paediatric Bronchiectasis Task Force.