Welcome to the Pulmonary Fibrosis Trust
The aim of the Pulmonary Fibrosis Trust is to provide personal support to people affected by Pulmonary Fibrosis, a very debilitating and life-limiting illness.
We offer practical, and emotional support where there is a need. We also raise awareness of the illness and in particular the challenges people face on a daily basis.
The Pulmonary Fibrosis Trust was founded by patients who experienced a lack of information and support upon their own diagnosis, and therefore, wanted to support others through this process.
We are here to support all those affected by pulmonary fibrosis, whether you are a sufferer or have a loved one with pulmonary fibrosis.
What is pulmonary
fibrosis?
Find out about pulmonary fibrosis symptoms, how it is diagnosed and treatment options.
Commemoration to Michel Roux
Chef Alain Roux, PF Trust Patron, commemorates his father four years after his passing.
Get involved to support others
Could you help by being an Ambassador or set up a fundraising event? Get in touch to find out more.
Support
available
From a listening ear to funding practical equipment, find out how we could support you.
Latest updates
See the latest updates from the PF Trust.
You can keep up to date with us by subscribing to our newsletter.
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….
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…
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…






