After the run, the story will live on through a 6-episode documentary series,
ensuring this moment continues to raise awareness long into the future.
Together, We Can Breathe Hope Into Lives
Pulmonary Fibrosis changes lives.
But with the right support, no one has to face it alone.
Every Breath is Precious
900 miles across Britain to help people living with Pulmonary Fibrosis breathe easier
One man running. Thousands fighting for breath.
Your support today helps people with Pulmonary Fibrosis feel less alone — and gives hope where breath is running out.
Give Breathe All Year Round
People living with Pulmonary Fibrosis face this condition every day.
Monthly gifts help us plan ahead, keep support services running, and be there when breath feels hardest to find.
By joining The Breath Circle, you become part of a community giving reassurance, dignity and hope — not just once, but all year long.
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
Your Gift Helps Someone Breathe Easier
Pulmonary Fibrosis takes breath away day after day.
Your support helps us be there — with care, understanding and hope.
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
Give Breathe All Year Round
People living with Pulmonary Fibrosis face this condition every day.
Monthly gifts help us plan ahead, keep support services running, and be there when breath feels hardest to find.
By joining The Breath Circle, you become part of a community giving reassurance, dignity and hope — not just once, but all year long.
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
Your Gift Helps Someone Breathe Easier
Pulmonary Fibrosis takes breath away day after day.
Your support helps us be there — with care, understanding and hope.
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 £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
Challenge Donation Tracker
How Your Support Makes a Difference
There are many ways to support Every Breath Is Precious:
Donate (one-off or monthly)
Join our regular giving community — The Breath Circle
Become a corporate partner or matched giver
Fundraise in your community
Share the campaign and raise awareness
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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Mastering Your Crown
During lockdown Emma wrote a book called ‘Mastering Your Crown; A Guide to Transforming Anxiety, Fear, Loss and Grief in Times of Crisis’ which was largely inspired by her wonderful mother but also because she could see so many people struggling mentally and emotionally with anxiety, fear, loss and grief. Sadly, Ann, Emma’s mother passed away …
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Pantomime Charity Event
Lynne was diagnosed with pulmonary fibrosis almost 2 years ago, and no one in her village had heard of the condition. The committee for the Amateur Dramatics (Russell Players) very kindly decided to support Pulmonary Fibrosis Trust by hosting a pantomime called Goldilocks, Three Bears and the Detectives which starts on November 19th. Peter Bryce, …
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Show your support this festive season
The countdown to Christmas has started and we are excited to present this year’s PFT Christmas card designs. Choose from the Fluffy Robin, Christmas mail, the Cute Deer or the Snowman’s buddy. Each pack contains one design and includes 10 cards and 10 envelopes. We ask for a £5 donation for each pack ordered which …
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Lucy runs Alton Towers half marathon
Lucy will be running the Alton Towers half marathon on 13th November 2022 and will be raising money for PF Trust along the way, as it’s a charity very close to her heart and is affecting her family. Her grandpa was diagnosed with pulmonary fibrosis in 2016 and two of his siblings were also diagnosed …
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Pulmonary Fibrosis Trust Charity Manager
Location: Home-based role with occasional travel Closing date: 14th November 2022 Interview dates: Interview dates to be confirmed Hours: 16 hours per week Salary: £12,000 The Pulmonary Fibrosis Trust provides personal support to people affected by Pulmonary Fibrosis, a very debilitating and life-limiting illness, which affects the lungs. The charity is growing in the number of people it …
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March Hare and Hare Beer Bunch London Bridges Challenge
Janice and John Pritchett who own the March Hare pub have done several fundraisers this year which is absolutely amazing. Janice kindly let us know how the most recent fundraiser went. “Our intrepid explorers, Mike, Simon and Keith successfully completed the March Hare and Hare Beer Bunch London Bridges Challenge, including visiting a few pubs …
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Call for participants
My name is Karima and I am a freelance photographer based in Coventry. I am working on a photograhy project based on people suffering from Pulmonary Fibrosis ( idiopathic or not ) and their loved ones/carers. I would like to take photographs of people willing to share their daily experiences and fights surrounding this illness. …
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Post run feelings
In June 2022 Nick Ashill went back to America to complete his goal of running across it. Nick was tragically struck down by a lorry whilst trying to complete this in 2017. After being told he would never walk again, Nick completed the rest of his run across America this year. Nick was kept company …
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Welcome to our new website
We have some very exciting news for Pulmonary Fibrosis Awareness Month. The countdown is over and we are excited to present the new website for the PF Trust! We’ve got a fresh new look and designed with your needs in mind. Some of the great new features of the website include enhanced resources and support. …
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Dave’s 60th birthday fundraiser
Emma, Dave’s wife, got in touch with the PF Trust earlier this year to tell us that they are hosting a birthday party at their local golf club to celebrate Dave’s 60th in June. Emma kindly shared some great photos of the day and let us know how the day went. They raised an amazing …
Community
There is a strong pulmonary fibrosis community sharing experiences and providing support.
As a part of the community, the Pulmonary Fibrosis Trust has a platform available to all to raise awareness and provide support to each other.
Make sure you follow us on social media and join our PF Trust Community mailing list. We welcome stories, experiences and tips and share these with the community via our newsletter.
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