With our help you can take the holiday of a lifetime.
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  • Every year we help to fund holidays and short breaks for children (under 18) 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 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.


IMPORTANT – Changes to holiday grants

ALL under 18s apply to the CF Holiday Fund

ALL over 18s apply to the CF Trust

From 1 April 2016, the Cystic Fibrosis Trust and the CF Holiday Fund are making some changes to how holiday grants are awarded.

The CF Holiday Fund will now fund and administer grants for people with cystic fibrosis aged under 18 only.

The Cystic Fibrosis Trust will now fund and administer grants for people with cystic fibrosis aged 18 and over.

These changes allow the two organisations to focus on providing grants for children and adults respectively, to administer the grants more effectively and ensure as many holiday grants as possible are distributed to those most in need.

For more information on adult holiday grant applications please follow the link below:

Or contact the CFT on:
Cystic Fibrosis Trust
One Aldgate
Second floor
London EC3N 1RE
0300 373 1000