Leicestershire 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 - patients, family, carers and friends.

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

When we meet

Second Thursday each month, 1.30pm - 3.30pm
If you are interested in joining our meetings please contact the support group lead above for further details.


Upcoming dates

Thursday 13thJune - Dr Barbara Powell, Loros Palliative Care

Thursday 11th July - Ron & Maxine Flewett, Lung Transplant/PF Trust/Carers

Thursday  8th August - Felix Woodhead

Thursday 12th September - Helen Molesdale, PF Rehab

Thursday 10th October - Chris Startup, Singing for Lung Health

Thursday 14th November - Cathy Jackson-Read, Action for Pulmonary Fibrosis

Thursday 12th December - To Be Confirmed



Where we meet

Ulverscroft Activity Centre
Ulverscroft Manor
Priory Lane
Ulverscroft
Leicestershire
LE67 9PH

Get directions on Google Maps