Cystic Fibrosis is a complex condition, affecting not only the lungs, but the pancreas, liver and other organs too. While our knowledge and understanding of CF, from its underlying genetic causes to ways of treating it, have grown immeasurably, there is still much to do if we are to reduce its impact on people with CF.

From the very start, back in 1964, the Cystic Fibrosis Trust has invested in research into all aspects of CF. We continue to be one of the largest funders of research into CF and, with our partners in the UK and internationally, we are committed to unlocking the secrets to treating - and beating - CF.

In this section, you will find the areas of research that we are funding directly and an overview of other research being carried out by our partner organisations across the world.

Fill in our survey and raise £20,000 in 20 minutes

We need 400 people with CF, over the age of 18, to complete a quick survey. For every person who fills it in, the Cystic Fibrosis Trust gets £50. That's £20,000 towards supporting people with CF live more fulfilling lives.

There's very little research about the Health Related Quality of Life (HRQL) of people with Cystic Fibrosis. In many counties including the UK, the decision to agree to fund a new treatment can only be made if HRQL information is available.

So, if you're 18+ and have Cystic Fibrosis, you can help. Please fill in our survey