Action for Pulmonary Fibrosis - Information and support
APF is a nationwide UK charity. We bring people together to drive change so more people affected by pulmonary fibrosis (or lung scarring) can live well for longer. We provide expert support, information, education, help a growing network of support groups and raise awareness of pulmonary fibrosis. We collaborate to drive change that improves health and care and we provide vital resources to researchers, bringing hope for new and future treatments for this devastating disease.
Remote
In-person
Further info
Support - There are over 100 independent Pulmonary Fibrosis Groups across the UK offering emotional support, helpful information, practigal guidance & signposting for anyone affected bfy Pulmonary Fibrosis. Local groups: APF Support Groups.
Support Line 01223 785 725 - Trusted compassionate support and information:
Information and Education - We provide a range of print and digital information for people affected by pulmonary fibrosis, their loved ones & health professionals. We offer bi-monthly webinars on all asspects of PF by a team of experts and people with lived experiece. Checkout our website actionpf.org
Awareness- Raising the profile of PF and tackling stigma and misinformation.
Advocacy- Campaigning for faster diagnosis, better care and health equality.
Research - Funding and influencing science that improves lives and brings hope.
Who can use this service?
Anyone affected by Pulmonary Fibrosis, including friends, carers, loved ones and health/social care professionals. Our telephone support line offers non-emergency support for people living with pulmonary fibrosis. We are unable to give individual medical advice.
How are services delivered?
Support Line 01223 785 725
Website actionpf.org
Face to face via our local Support Groups. To find a support group near you visit: APF Support Groups.
Locations