Action for Pulmonary Fibrosis (APF) is a growing community of patients, families, researchers and healthcare professionals striving to find a cure for pulmonary fibrosis so that everyone affected by the disease has a better future. We provide personalised support to patient and families - and raise awareness of pulmonary fibrosis through campaigning, fundraising and education. We are also committed to funding research to improve the quality of life for people living with pulmonary fibrosis today and tomorrow.

Sadly Helens Dad succumbed to this horrible disease late last year. Helen felt that she wanted to do something in aid of her Dads memory and to support a growing charity in striving to find a cure for a disease that is more common than you realise yet relatively unheard of and under supported.

The idea was born from an office chat and evolved to  signing up for an event that was an achievable challenge to kick start our fundraising which we’re hoping to build on.

Any Donation big or small would be gratefully received  and Thankyou we hope to do you and Helen’s Dad proud!