Our volunteers give their time, experience and expertise to help us promote lung health and support people living with lung conditions. Without their support, we simply would not be able to do what we do. You can learn more about some of them here.
Zena has worked alongside ELF since 2019 as a parent-patient advisory member on non-cystic fibrosis bronchiectasis in childhood. Her son Ed was diagnosed with bronchiectasis 9 years ago, having first showed symptoms at 5 months old.
Zena's role within the Childhood Bronchiectasis PAG has included getting involved on the Taskforce to produce guidelines and set future research priorities. Since 2021, she has also been an active member of Child-BEAR-Net and sits alongside Ed on the ELF Core Council.
