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Pulmonary Fibrosis Trust

Pulmonary Fibrosis Trust

Every breath matters

  • About the Pulmonary Fibrosis Trust
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01543 442 191

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        • About the Pulmonary Fibrosis Trust

        • Latest updates

          • Pulmonary Fibrosis Trust Welcomes Approval of New Drug
          • Chair Peter Bryce Word on Health Interview
          • ‘At 53, I was told I’d never walk again. At 62, I’m running the length of Britain – here’s how I fought back’
          • Jacob’s Ground Hopping Journeys
          • Nick Runs Britain: 900 Miles for the Pulmonary Fibrosis Trust
        • About
          • About the Pulmonary Fibrosis Trust
          • PFT Patron – Alain Roux
          • Meet the Trustees
          • Ambassadors
          • Research
        • Contact us
  • Support
        • Support

        • About Pulmonary Fibrosis
          • What is pulmonary fibrosis?
          • Diagnosing Pulmonary Fibrosis
          • Monitoring and management
          • How to help yourself
          • Allowances available
        • Support available
          • Emotional support
          • Equipment funding
          • Caravan holidays
          • Useful links
  • Get involved
        • Get involved to help others

        • Be inspired

        • Every donation helps

        • Donate
        • Memorials
        • Merchandise
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          • Fundraising stories

News

Home - News - Page 2

Fundraising Information Guide

We are very excited to launch our fundraising information guide, which is a 12 page booklet to support the amazing people who fundraise for our charity! Get yours now, and see how you can help someone living with pulmonary fibrosis.

Read moreFundraising Information Guide

Jayne’s mobility scooter

We fund mobility scooters, wheelchairs, and other mobility aids. The mobility aids transform people’s lives and allow them to spend quality time with their family. Jayne contacted us to help with funding for a mobility scooter at the end of last year, and she told us how having a scooter made such a difference. “I …

Read moreJayne’s mobility scooter

Great North Run 2024

We have places available for the Great North Run and would love you to run for you or someone you know to be part of our running team! Make a difference today and sign up to raise funds for research to finding a cure to pulmonary fibrosis, or giving someone back their independence by funding …

Read moreGreat North Run 2024

Saving Your Breath

Taskforce for Lung Health and Asthma + Lung UK have launched the “Saving Your Breath” campaign. It’s a call to action to ensure that individuals living with lung conditions receive the care and treatment they deserve. Read the full report here.

Read moreSaving Your Breath

ILD-IN conference 2023

It was a pleasure to attend the ILD IN conference, and meet so many inspiring and wonderful people. It’s amazing to hear about the incredible work being done by ILD-IN, and how we can help support those with PF patients. For those who did not attend, please get in touch to see how we can …

Read moreILD-IN conference 2023

Pulmonary Fibrosis Awareness Month

September marks Pulmonary Fibrosis (PF) Awareness Month, a globally recognised awareness initiative aimed at raising awareness about the disease, its symptoms and the need for support.  Help us raise awareness of pulmonary fibrosis this September, as well as the support and resources the Pulmonary Fibrosis Trust can offer.  The more people that are talking about Pulmonary …

Read morePulmonary Fibrosis Awareness Month

Welcoming our first Patron, Chef Alain Roux

Pulmonary Fibrosis Trust announce their first Patron – Chef Alain Roux 23rd June 2023 – The Pulmonary Fibrosis Trust are delighted to announce the new Patron of the Charity – Chef Alain Roux. Chef Alain, world famous and celebrated chef, takes on the patronage in memory of his father, Michel Roux OBE, founder of world …

Read moreWelcoming our first Patron, Chef Alain Roux

Great North Run 2023

We have places available for the Great North Run and would love you to run for you or someone you know to be part of our running team! Make a difference today and sign up to raise funds for research to finding a cure to pulmonary fibrosis, or giving someone back their independence by funding …

Read moreGreat North Run 2023

GKA Idiopathic Pulmonary Fibrosis

GKA, a UK based medical market research agency, are looking to speak to individuals living with Idiopathic Pulmonary Fibrosis. We are currently undertaking a research project to consider how we can improve individuals experience of taking part in clinical trials. Please note that this is not a clinical trial, but a simulated experience. Who: This …

Read moreGKA Idiopathic Pulmonary Fibrosis

Goodbye AmazonSmile

Unfortunately Amazon have announced they will be closing their AmazonSmile program this month. Thank you to everyone who signed up and donated, we are very grateful for your support. £1,730.50 has been raised in the last few years so thank you so much to all who signed up! 💙 💜

Read moreGoodbye AmazonSmile
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Our community is for ALL those affected by pulmonary fibrosis. Whether you are a PF/IPF sufferer, family or friend, healthcare professional or interested in raising awareness of pulmonary fibrosis, you are all welcome.

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01543 442 191

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Pulmonary Fibrosis Trust
c/o EBS
Stowe House
St Chad’s Road
Lichfield
Staffordshire
WS13 6TJ

Pulmonary Fibrosis Trust is a Charity registered in England with number 1213302
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