Pulmonary Fibrosis Trust
Every breath matters
PFT Patron Nick Ashill is preparing to run 900 miles from John O’Groats to Land’s End this September to raise awareness for everyone living with pulmonary fibrosis. Nick recently spoke to Runner’s World about the challenge, his extraordinary journey, and why raising awareness of PF matters so much. Read the full article here: https://www.runnersworld.com/…/running-length-of…/ Find …
PFT ambassadors Kenny and Jacob McDonald are back on the road again and this time they’re taking on all 42 Scottish football league stadiums to raise awareness of pulmonary fibrosis and support the Pulmonary Fibrosis Trust. As part of Jacob’s Ground Journeys, the pair will visit every SPFL ground across Scotland and complete 10 laps …
Get involved: PFT Every Breath Club: 900 Miles with Nick 2026 | Pulmonary Fibrosis Trust Details about the run: Nick Runs Britain: 900 Miles for the PFT 900 miles. One mission: Help People Breathe British ultrarunner to take on the length of Britain for a devastating lung disease, with the nation invited to join …
The Pulmonary Fibrosis Trust are proud to be closely linked with ILD-IN.Our patron Alain Roux recently met up with ILD-IN Co chair Marium Navqi for a fireside chat at The Waterside Inn, to discuss his family’s experience with pulmonary fibrosis
Every 5 minutes, someone dies from a lung condition in the UK. And yet there’s a lack of political will to fund the research that could save these lives. Today, the Lung Research and Innovation Group have set out 10 priorities the government needs to take seriously to fix the lung research pipeline and fix …
All our places for the Great North Run 2024 are full, but if you are running for us through the ballot then please get in touch as would love to support you! If you wish to run for us in 2025, please contact us now to be added to the waitlist. Contact us today by …
Seven-year-old Jacob will be out to conquer his biggest feat ever by walking the Humber & Severn Bridges both ways in July
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.
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 …
