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
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Thank you to Leicestershire PFSG
Thank you so much to the Leicestershire Pulmonary Fibrosis Support Group who invited our chair, Peter Bryce, to give a presentation on what our charity…
10 miles a day in January
Thank you so much to James who has been running an amazing 10 miles every day in memory of his father in law, Gary Dean…
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…
Thank you Jobie!
We would like to say a massive thank you to Jobie Travers, our ambassador, for all the hard work he has done over the years….
PFT Charity Single ‘Christmas Time’
‘Christmas Time’ Song Bio: Written for The Pulmonary Fibrosis Trust, Ambassador Ben Drake, wanted to try and capture the spirit of Christmas, being thankful for our…
Well done Jacob!
How amazing that Jacob’s school devoted their assembly to pulmonary fibrosis and all the fundraising Jacob has done. They presented him with a certificate which…