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This year we're talking time and hearing from Michelle, Chloe, Amy and Dom, who are all affected by cystic fibrosis.
Put on your sunniest outfit on 22 June 2018 and help us paint the country yellow to raise awareness and funds for our vital work.
A new data laws mean we can no longer email you to tell you about the impact your support is having - unless you give us your tick.
Explore our brand new Trials Tracker and loads of useful resources on our Clinical Trials Digital Hub.
Find out about our campaign for access to precision medicines and the upcoming debate in parliament.
Take a look at our interactive body to see exactly how CF affects the body.
Sign up to our e-newsletter to hear the latest news on what the Trust and its supporters are doing to fight for a life unlimited.
Take a leap of faith at 10,000 feet and parachute back down to earth as you take on a Skydive!
With 20 drop zones in the UK to choose from and on a date of your choice there's no reason for you not to take on this challenge of a lifetime.
Jeremy Hunt, Secretary of State for Health and Social Care today called on drug manufacturer Vertex to be transparent on its pricing for the precision medicine Orkambi, and agreed to explore avenues for ensuring quicker access to medicine, in a session of oral questions on health, in Parliament today.
We invest more money into cystic fibrosis research than any other UK organisation.
Find out more about our vision for a life unlimited by cystic fibrosis for everyone with the condition, and our strategy for getting there.
If you have a question, query, comment or suggestion, we'd love to hear from you.
Discover answers to frequently asked questions about cystic fibrosis.