The Pulmonary Fibrosis Trust would like to hear from PF sufferers, on how long they waited for diagnosis and referrals. We would be grateful if you would complete the 3 questions by clicking the link below.

Great News! We are pleased to announced that bookings are now open for our holiday home in Great Yarmouth. Please go to our website to download the application form or email us on info@pulmonaryfibrosistrust.org.

We have a few places for the Great North Run 2025, if you would like to run for the Pulmonary Fibrosis Trust please contact us for more details. Places are limited.

From all of us at Pulmonary Fibrosis Trust, we would like to thank everyone who has fundraised, donated or supported us in 2024. Thank you so much.

From all of us at Pulmonary Fibrosis Trust, we would like to thank everyone who has fundraised, donated or supported us in 2024. Thank you so much.

Thank you to Yardley Pharmacy, who did a bake sale and raffle and raised over £600 for the PF Trust.

We would like to thank the family of Phyllis Hewitt for the donation we have received in her memory. From all of us at PFT, Happy 80th Birthday.

The Pulmonary Fibrosis Trust are pleased to be in attendance at the ILD-IN conference in Edgbaston 06-07 October 2024.

New video featuring chair Peter Bryce and Patreon Alain Roux live on our Facebook page. #PFAM #EveryBreathEveryStory

Welcome, to our new trustee Lynsey Conway: Lynsey has spent over 30 years working in the health sector providing communications and public affairs support. Lynsey lives with her husband, teenage son, and nutty Spaniel, Daisy. #PFAM #EveryBreathEveryStory

A huge thank you to Helen Bridgeman in completing the GNR in aid of PFT. I managed to do it in 2 hours and 58 minutes, which was just under my goal of 3 hours. I can't thank you all enough for the donations, love and support I have been shown. #PFAM #EveryBreathEveryStory

Meet one of our trustees Jessica Sharp: I became an Ambassador for the Pulmonary Fibrosis Trust in 2014 after losing my Uncle to IPF. Not having heard of PF before, I was determined to make it known by raising awareness. #PFAM #EveryBreathEveryStory

Please join us in congratulating the Princess of Wales Hospital team for completing their run and raising an absolutely incredible £800 for far!! #PFAM #EveryBreathEveryStory

I particularly liked the fact that the PFT helps patients & their families on a practical level & it really does make a difference. On another note when I'm not working or doing Trustee things you can find me reading, at the theatre, travelling or sometimes even swimming! #PFAM

As shown in our patient and carer survey, an astonishing 9 out of 10 people had never heard of #pulmonaryfibrosis before they were diagnosed. With over 70,000 people living with IPF in the UK, more needs to be done. 💙💜 #PFAM #EveryBreathEveryStory

Many people when first diagnosed have never heard of #PulmonaryFibrosis, or the devastating impact it can have on them or their family. With so many people diagnosed every year it's important to raise awareness so that more people know about PF and where to seek support. #PFAM

Thank you, to one of our Great North runners, Vicky #PFAM #PFMonth #PFTrust

Thank you to our GNR Heroes! Every step & mile you conquered brings us closer to improving the lives of those affected by Pulmonary Fibrosis. Thank you for being part of our mission. Your efforts make the difference. We couldn’t do this without you! #PFAM #EveryBreathEveryStory

🚴‍♀️ In memory of her late husband, Susan Macleod is riding 980 miles from Land’s End to John O’Groats to raise funds for the PFT. ❤️ "Francis will be with me in spirit. With the support of family & friends, nothing is insurmountable." 💪 #PFAM #BabbleRideAcrossBritain