Donate £9
To symbolically sponsor a mile of the journey
Donate £9
To symbolically sponsor a mile of the journey
Donate £9
To symbolically sponsor a mile of the journey
Donate £9
To symbolically sponsor a mile of the journey
Donate £9
To symbolically sponsor a mile of the journey
Donate £9
To symbolically sponsor a mile of the journey
Donate £9
To symbolically sponsor a mile of the journey
Donate £26
to represent one day of running
Donate £50
to help fund vital patient support
Donate £100+
to fund life-changing home adaptations
Donate £9
To symbolically sponsor a mile of the journey
Donate £26
to represent one day of running
Donate £50
to help fund vital patient support
Donate £100+
to fund life-changing home adaptations
Strava feed
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Welcome to our new Trustee
We are very excited to announce that Debbie Roots is now a Trustee for the PF Trust! Read more on who Debbie is and why she wanted to become a Trustee in her own words. Let me introduce myself, I am currently working as a respiratory nurse consultant and have a vast amount of experience …
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Places for London Virtual Marathon 2022
Do you know someone who wants to take on an amazing challenge whilst helping support people who are living with pulmonary fibrosis and their family today! We have places available for the London Virtual Marathon and would love you to spread the word and share this post! Runners are asked to pay a non refundable …
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Welcome to our new Trustee
We are very excited to announce that Jess Sharp who was previously an Ambassador for the PF Trust, is now a Trustee. She kindly said a few words about her reasons why she wanted to become a Trustee. After loosing my uncle to IPF in 2014, I got in touch with the Trust asking if …
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International Nurses Day 2022
Today is International Nurses Day. Everyone at the PF Trust thanks all nurses out there working so hard to look after every patient, including those with IPF and PF. Respiratory nurses, ILD nurses and nurses in general are very much appreciated by the PF community and we thank you for all that you do.
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PF Trust at the ARNS Conference
The PF Trust had a fantastic time at the ARNS conference on May 6th and 7th. It was great to be back at a face to face conference and get to meet everyone again. Thank you to all who visited our stand. We hope that we can reach more people who need our help.
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Community
There is a strong pulmonary fibrosis community sharing experiences and providing support.
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