“What’s pulmonary fibrosis?” A personal story from Peter Street

Earlier this month, Peter Street got in touch with the Pulmonary Fibrosis Trust and shared the story of his diagnosis with us. Peter has spent much of his life writing — as a published poet, memoirist and writer-in-residence. When pulmonary fibrosis unexpectedly became part of his own story, he did what he does best and…

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World Lung Day 2026

World Lung Day 2026 On World Lung Day, the Pulmonary Fibrosis Trust stands alongside people across the world living with lung disease, their families, carers and the healthcare professionals who support them. Pulmonary fibrosis remains a condition that far too many people have never heard of until it affects them or someone they love. That…

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Statement from the Pulmonary Fibrosis Trust on NICE Draft Guidance for Nerandomilast

The Pulmonary Fibrosis Trust is deeply disappointed by NICE’s draft decision not to recommend nerandomilast for routine NHS use in people living with idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF). As one of the organisations participating in the consultation process, alongside Asthma + Lung UK and Action for Pulmonary Fibrosis, we are currently…

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Nick Runs Britain: 900 Miles for the Pulmonary Fibrosis Trust

Get involved: PFT Every Breath Club: 900 Miles with Nick 2026 | Pulmonary Fibrosis Trust Details about the run: Nick Runs Britain: 900 Miles for the PFT   900 miles. One mission: Help People Breathe British ultrarunner to take on the length of Britain for a devastating lung disease, with the nation invited to join…

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Fire Side Chat at The WaterSide Inn

The Pulmonary Fibrosis Trust are proud to be closely linked with ILD-IN.Our patron Alain Roux recently met up with ILD-IN Co chair Marium Navqi for a fireside chat at The Waterside Inn, to discuss his family’s experience with pulmonary fibrosis  

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