Big thanks to all the attendees at our @DHealthLDN showcase today. In particular we'd like to thank Kay Boycott our chair, Our fantastic clinician speakers Laura Lowndes & @mwickremas and our inspirational patient speaker @TriathARon#DigitalHealthLondonTurns5
Pulmonary Fibrosis Transplant Patients Support Group. Next meeting on 8 October 1600-1730. Contact: [email protected] [Photo shows group members @ActionPFsteve (5 years post-transplant) and @TriathARon (on active list) out for e-bike ride] @ActionPFcharity
“Reversing PF should be our goal. But it’s not just about finding better treatments, it’s about finding ways to identify patients with PF earlier before there is a lot of scar tissue and fibrosis.” (Toby Maher)
#PFSummit21#PF#PFmonth#BreathingLife#pulmonaryfibrosis
To clinicians, carers, researchers and others: Join us and help raise awareness of #PF! “Awareness campaigns play an important role in getting patients to see a general practitioner and avoid delayed diagnosis.“ (Marlies Wijsenbeek)
#PFmonth#BreathingLife#pulmonaryfibrosis
When #PulmonaryFibrosis develops, it's probably not sudden changes you instantly notice - and that's part of the problem. Learn more about recognizing the signs on a new episode of the Journeys through Pulmonary Fibrosis podcast.
There are many ways to keep fit and improve your quality of life – like Ron on his electric bike: „It has enabled me to carry on doing what I love doing.” (Ron Flewett)
#PF#PFmonth#BreathingLife#PFAwarenessMonth#qol
Despite IPF being such a serious disease, there are still ways to enjoy life: "A chronic disease is an adjustment of life – not the end of it. There will have to be adjustments along the pathway." (Liam Galvin)
#PFSUMMIT21#PF#PFmonth#BreathingLife#PFAwarenessMonth#qol
Watch our video interview with #IPF patient activist Ron Flewett @TriathARon exploring the impact of the pandemic on #IdiopathicPulmonaryFibrosis patients and how home monitoring of FVC & FEV1 was a “huge reassurance during COVID-19” #virtualcare https://t.co/r90n2yDxrU
Ron, one of our Trustees, has been speaking to ITV Calendar sharing his concerns for clinically extremely vulnerable people who have been shielding during the pandemic and worries how this will impact them with 'freedom day' today 💜💙🙌https://t.co/HrQLj9rAy7
Kicking off our 7th @EU_IPFF General Assembly, reporting to our members, advisers and supporters what the European Pulmonary Fibrosis Federation has done in the past year, what we will work on in 2021 and 2022 in patient advocacy and research. We'll also elect new board members!
Kicking off our 7th @EU_IPFF General Assembly, reporting to our members, advisers and supporters what the European Pulmonary Fibrosis Federation has done in the past year, what we will work on in 2021 and 2022 in patient advocacy and research. We'll also elect new board members!
Take a look at the moving segment featured in @itvcalendar yesterday, featuring @TriathARon and Alison Cook, Chair of the Taskforce, talking about the impact of delays to lung disease diagnosis and care: https://t.co/4KfJGf0RWg