Pulmonary Fibrosis Trust
Every breath matters
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 …
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, …
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 …
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 …
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 …
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 …
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. …
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 …
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. …
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 …
Could you help by being an Ambassador or set up a fundraising event? Get in touch to find out more.
Providing personal support to people affected by Pulmonary Fibrosis, a very debilitating and life-limiting illness.
Would you like to join the PF Trust's 2022 London Marathon Team or know someone who would?
Get in touch today to register your place.
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