Borders Pulmonary Fibrosis Support Group

Group of smiling people with PF information material
Information icon

Keeping well this winter
During the colder months, there might be a higher risk of catching coughs and colds when meeting face-to-face. If you're concerned about this, please speak to the group leader for information about how group members are keeping in touch, and how the group manages infection risk.

Read more about managing pulmonary fibrosis in cold weather.

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 will offer 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?

Contact details

Christine Evans
christineevans822@gmail.com

When we meet

We are a new support group and would love to hear from anyone in the Borders area whose life has been impacted by pulmonary fibrosis

We get together 2 or 3 times a year but keep in touch and support each other through a what's app group. If you'd like to join this group please contact Christine using the details above

Upcoming dates

For  more information about our group, please contact Christine

Where we meet

Get directions on Google Maps