UCLH Pulmonary Fibrosis Support Group

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Holidaying with pulmonary fibrosis
When you’re living with pulmonary fibrosis (PF), going on holiday might need a bit more planning and preparation. We’ve written this guide to help you think about your needs so you can enjoy your holiday.

Read more here.

Being diagnosed and living with a lung condition can be challenging. Support groups offer the opportunity to meet others who understand what you are going through and are open to anyone affected by pulmonary fibrosis - people living with pulmonary fibrosis, family, carers, and friends.

We will offer a range of speakers on topics such as singing for lung health, keeping active, healthy eating, mental well-being, travel insurance, and the latest news in research and treatments. Specialist staff are sometimes available for information and advice, and we also arrange informal specialist events from time to time. Why not come to one of our meetings and check us out?

Contact details

Julia Stoward

julia@actionpf.org

Alternate Months, 3rd Monday of the month.

Upcoming dates

18th March 1-3pm

20 May 1-3 pm

15 July 1-3 pm

16 September 1-3pm

18 November 1-3pm

Where we meet

Hatter Cardio Vascular Institute

67 Chenies Mews

London

WC1E 6HX

Get directions on Google Maps