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Our core content on Lung conditions and related factsheets has been translated to a number of other languages by our volunteer team.
For more languages explore all available Factsheet translations.
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Home » ELF Patient Organisation Networking Day 2022 Posters » Action for Pulmonary Fibrosis resources
Resources from Action for Pulmonary Fibrosis (APF).
Below are a few examples to highlight some of the self-management resources that the UK Charity Action for Pulmonary Fibrosis (APF) have available. Their self-management resources can either be viewed, downloaded, or printed from their website https://www.actionpf.org/
A panel involving a clinical nurse specialist, patient and chair of APF, patients and a carer discuss their journey and experience living with PF. The session includes common challenges faced, what support is available and how to access this.
Handy tips and advice on how to manage breathlessness when bending. This is one of the most visited support pages on the APF website.
https://www.actionpf.org/information-support/managing-breathlessness-when-bending
Information on the APF website is available in a tidy print format for anyone visiting our website. They are also developing a healthcare professionals training and resources page to help with supporting patients and families living with pulmonary fibrosis.
https://www.actionpf.org/healthcare-professionals/training-and-resources
APF’s free magazine offers information and self-management tips to help you live well with PF and manage your condition more effectively. It also includes stories, research news and updates from their PF community.
You can sign up to receive the magazine via this link: https://www.actionpf.org/information-and-support/magazine
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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).
Our Brussels office enterprise number is 0738.383.695
European Lung Foundation's TR ID number in the Transparency Register is: 094039644810-79