Please get in touch at press@actionpf.org for any press/media enquiries.
Press releases
Action for Pulmonary Fibrosis launches new 5-year strategy to expand support and accelerate research
Action for Pulmonary Fibrosis appoints its first Patient President
Results of landmark clinical trial offer new hope for people living with pulmonary fibrosis
Johnnie Walker voices campaign to spot the signs and symptoms of lung scarring disease
New Chair of Trustees for Action for Pulmonary Fibrosis
New survey reveals staggering lack of awareness of killer lung scarring disease that's on the rise
More people living with IPF in Scotland to benefit from anti-fibrotic medication
Thousands of patients with terminal lung scarring given access to drugs that could prolong their lives
Action for Pulmonary Fibrosis BBC TV Lifeline Appeal
ACCELERATING CHANGE FOR PULMONARY FIBROSIS
One step closer for IPF patients to access life-extending anti-fibrotic drugs
NEW STATS REVEAL PEOPLE WITH PULMONARY FIBROSIS FEEL JUDGED FOR HAVING A PERSISTENT AND UNCONTROLLABLE COUGH
"Life With IPF" Podcast Released with patient Sylvia and Honey Langcaster-James
Janice Long joins forces with Action for Pulmonary Fibrosis for second year running
Patients call to end restrictions on drugs that prolong the lives of people with lung scarring
Increase in lung scarring or fibrosis, as a result of the COVID-19 pandemic.
Priority for pulmonary function tests (PFT) to early stage IPF patients.
Action for Pulmonary Fibrosis research brings hope to IPF patients and their families