Due to the coronavirus (COVID-19) outbreak, many of you will have had to cancel or postpone your fundraising events. We know this will be disappointing, but we also know that many of you will still want to get involved, keep active and have fun, and be assured we are here to support you in whatever you want to do during this difficult time.
Check out our virtual A-Z of fundraising ideas (237 KB) and remember we are here to help. Thank you so much for all your amazing hard work, enthusiasm and continued commitment, we are so grateful for all you are doing at this very difficult and challenging time.
Find out how you can organise a Big Bounce at your school or workplace, or with friends and family! You can download our 'how to' factsheet, your very own Big Bounce poster for your event and order a fundraising pack today.
Bouncing is a fun and easy way for people with cystic fibrosis to exercise and also helps to clear mucus from the lungs, which could otherwise attract infection. So what better way to raise money than by bouncing?
See what the pupils of Sandbach High School and Sixth Form College in Cheshire got up to when they dedicated their sports day to CF Week.
Organise your own Big Bounce
This campaign is all about bouncing, whether on space hoppers, trampolines, pogo sticks – anything that bounces! The key is to get creative.
You can hold your event at your school or your local hall, but if these are too tame why not try something more adventurous?
- Across bridges and back
- A race on a grand driveway to stately houses or castles
- A lap of a racecourse
- Along a seafront promenade or the beach
- On woodland trails or disused railways
- Around the grounds of stadiums
So what to do on your bounce? Create an assault course, bounce at work, hire a bouncy castle, have a race – there are all kinds of challenges you can set. For more ideas and further guidance or organising your event, download your How to Big Bounce.
Advertise your event with our Big Bounce Poster.
Order your Big Bounce fundraising pack today on 020 3795 2176 or email firstname.lastname@example.org. Remember to include your name, address and daytime telephone number.
Research we fund
We fund research to tackle some of the most pressing issues in CF today. Find out how your donations are making a difference.
What is CF?
Cystic fibrosis, or CF, affects the lungs, digestive system and other organs, and there are over 10,600 people living with it in the UK.
Get in touch with us to speak to someone on our Helpline, find out about an event or speak to our Press Team.