Pulmonary Fibrosis Trust
Every breath matters
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 …
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 …
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.
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 …
