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.



Unfortunately the Cystic Fibrosis Holiday Fund will be unable to process further holiday grants from the 1st July for the remainder of 2016.

We will resume activity from January 2017. An unprecedented demand for grants in the first half of this year has exceeded the funds at our disposal. We will continue to focus on activities that will generate the required funds for 2017 and we would, as always, encourage everyone involved with the charity to lend a helping hand.

Any fund raising activity, grant or donation, however big or small, will be gratefully received.

Please do not hesitate to contact us, should you require any further information or support for your fundraising activity.

Email info@cfholidayfund.org.uk

Tel 020 7616 1300