ELF is pleased to partner with lung health organisations around the world to announce the first World Bronchiectasis Day, which will be held on 1 July 2022. The day will be held each year with the aim to raise global awareness of bronchiectasis and help those affected by the condition through education and advocacy.
Bronchiectasis is a lung disease that affects hundreds of thousands of people worldwide. It causes enlarged or scarred airways that cannot clear mucus properly, resulting in recurring lung infections. Although there is currently no cure, detecting and managing bronchiectasis early can improve quality of life and increase life expectancy of those affected.
World Bronchiectasis Day has been initiated by the COPD Foundation, USA. Representatives from ELF and other global patient advocacy organisations and professional societies serve on the organising committee.
“By supporting World Bronchiectasis Day, global partners are committed to addressing the critical unmet needs of the bronchiectasis lung disease community,” said Ruth Tal-Singer, PhD, COPD Foundation President & Chief Scientific Officer.
ELF has a strong community of bronchiectasis patients and a dedicated website (https://www.europeanlunginfo.org/) for people living with the condition. Watch the first-hand story of living with bronchiectasis by Barbara Crossley, member of the ELF Bronchiectasis Patient Advisory Group.
ELF hopes that World Bronchiectasis Day will help give patients across the globe a stronger voice and better care.
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ELF is a non-profit organisation registered as a UK company (VAT no. GB 115 0027 74) and charity (no. 1118930).
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European Lung Foundation's TR ID number in the Transparency Register is: 094039644810-79
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