With our help you can take the holiday of a lifetime.
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CYSTIC FIBROSIS HOLIDAY FUND

  • 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

 

Jonathan
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.

 

UPCOMING EVENT

SPRING 2015 Date TBD!

Get ready for Comedy Night 2015!

Thank you to Howie Baws, tireless fundraiser and amazing person for once again pulling together this event. See you at the Comedy Club!

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WE ARE LOOKING FOR AN INTERN FOR OUR LONDON OFFICE, PLEASE CONTACT info@cfholidayfund.org.uk FOR MORE INFO