Feeling abandoned? A new Pulmonary Fibrosis Carers’ Support Group is here for you…

White cup of coffee on a tan background
27
September 2021

Are you interested in using your lived experience and voice to help us shape the future pulmonary fibrosis research?

The Pulmonary Fibrosis (PF) Carers' Support Group is run by and for carers to share experience on ways to make life better for you and the person you are supporting.

The group started as an APF focus group during lockdown last year, to help the charity develop support for carers. It has now developed into a national PF Carers’ Support Group which meets monthly online.

Former carer Wendy Jones, who’s mum had PF, is helping to facilitate the group. Speaking to the isolation that many carers' can experience, she shared:

“Carers have a vital role but caring can feel a lonely place. This group is open to all PF carers – you are not alone, we are here for you.”

For further information and the meeting link contact support@actionpf.org or phone 01223 785 725. We’d love to welcome you!