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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 can enjoy your holiday.
Contact details
Wendy Dickinson
07710015490
wdickinson1@gmail.com
Shama Malik
07889907157
Shama.malik@hotmail.co.uk
Website
Monthly on the last Tuesday in the month 12 for 12.30 start
Please check our Facebook page for further details - Nottingham Pulmonary Fibrosis Support Group. Alternatively you can call Wendy, Lead Contact for the group (as above)
Wendy, the support group leader, will be there to welcome you from 12 midday with the meeting ‘proper’ starting at 12.30pm until 2.30pm. Please feel free to bring your lunch with you! Tea, coffee and biscuits are provided.
Due to an increase in group numbers and therefore in the cost of a larger venue, we would be delighted if you could make a voluntary donation to the group when you attend a meeting - members have suggested £2 pp.
We also have a raffle so prizes are always welcome and we ask you to bring your own mug!
Upcoming dates
December 19th - Christmas Party including Christmas-themed Singing for Lung Health
Please bring a plate of food - sweet or savoury - to share. Fizz and soft drinks provided.
2024
January 30th
February 27th
March 26th
April 30th
May 28th
June 25th
July 30th
August- date tbc - Summer Outing
September 24th
October 29th
November 26th
Where we meet
Sir Julian Khan Pavilion,
West Park,
Loughborough Road,
West Bridgford,
Nottingham,
NG2 7JE.