With our help you can take the holiday of a lifetime.
Slideshow Image 1 Slideshow Image 2 Slideshow Image 3 Slideshow Image 4 Slideshow Image 5


  • Every year we help to fund holidays and short breaks for children and young people (under 25) with Cystic Fibrosis
  • As many as 9,000 people in the UK suffer from this debilitating disease. CF dominates their everyday routine and significantly reduces their life-span
  • Here at the Cystic Fibrosis Holiday Fund, our aim is to offer children and young adults with CF a respite from the disease. Holidays are imperative for the physical and mental well-being of those we help, and just about the only time during the year a family can spend quality time together, share new experiences and create wonderful, carefree memories.
  • With your help more CF-sufferers could enjoy the holiday of a lifetime and do something they have always wanted to do – from taking a round-the-world trip to spending a weekend in London or Paris


Jonathon visited Disney World and Universal Studios in Florida. The Cystic Fibrosis Holiday Fund provided a grant for travel and arranged for free tickets to the theme parks.


Great news!

We have received funding on a limited trial basis from the CF Trust to give anyone with CF over 25 the chance to apply for a holiday grant. Just click on the “apply” page to find out more!