Please note that the meeting of the support group at Guy’s Hospital has been brought forward from the 9th May to the 2nd May. This is because of room availability. For further details on the support group click here
Sometimes it can help to hear how others have learnt to live with IPF. Watch the inspiring stories of people living with the disease, including their challenges and triumphs. Produced by Boehringer Ingelheim, enabled by Action for Pulmonary Fibrosis. See the stories here.
Action for Pulmonary Fibrosis has led the largest ever survey of people living with idiopathic pulmonary fibrosis (IPF) – an incurable lung disease which kills 6,000 people each year – in the UK has discovered high levels of misdiagnosis. The report, Giving Patients a Voice has been published today (12 March 2019). What did the report find? More than […]
American Thoracic Society (ATS) Travel Fellowships Action for Pulmonary Fibrosis would like to support researchers working in pulmonary fibrosis to attend the ATS 2019 in Dallas, Texas. The awards of £1000 contribute towards costs for conference registration, accommodation and travel. We have three awards available. Applications are now invited from any UK based researcher […]
It’s #RareDiseaseDay 2019. Contrary to public perception pulmonary fibrosis is not a rare disease. It’s under-resourced, under-recognised and often forgotten. Over 6,000 people are diagnosed a year and numbers are increasing. Read more
Choral Diversity performed a Christmas Concert, and raised a fantastic £900 for Action for Pulmonary Fibrosis. Melissa Hippard has IPF, and her very talented daughter Beth Melling is the founder and musical director of the Hereford and Ludlow based choir Choral Diversity -pictured above. We’d like to thank Beth and all the choir members for […]
Quoting Harriet “Well today I completed challenge 2, 40k Stonehenge Stomp! It was exhausting but I did so much better than I thought I would, I managed to run the majority of it apart from the steep hills. I did it in 4hrs 47 mins which I was really pleased with. And the weather didn’t […]
Wendy Dickinson and brother Philip Taylor The children of former Nottingham Forest and Derby County legend Peter Taylor have announced they are donating the royalties from the publication of a book written by their father about his career with Brian Clough to medical research. The book will be available on Thursday 24 January 2019. Peter […]
HYWEL DDA Pulmonary Fibrosis Support Group meeting on 19th December, at 3pm till 5pm. It’s at St Marys Catholic Church, 2 Union Street, Carmarthen, SA31 3DE All welcome.
The Bedford Pulmonary Fibrosis support group is meeting on Tuesday 18th December 2.30 to 4.00pm at the Jubilation Centre – the Biddenham Bell Ringers will be coming.