CYSTIC FIBROSIS HOLIDAY FUND
- Every year we help to fund holidays and short breaks for children (under 18) with Cystic Fibrosis
- As many as 10,000 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 respite to children with CF. 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, and with project Revitalise World-Wide, CF sufferers can enjoy the holiday of a lifetime.
Exciting Developments at the CFHF
The CFHF will next be assessing grant applications in January 2017. The new online form is fully operational and ready for your application. Look out for the revised FAQs to help guide you through the process of applying to us online. If you have any further questions please do not hesitate to contact us by phone or email.
Tel 020 7616 1300
Project ‘Revitalise World-Wide’
In 2017 the CFHF will be partnering with an international holiday provider to enable families struggling with CF to get a break that would not take place without our help. Studies have shown that holidays give CF sufferers a measurable improvement in both physical and mental well being and this is our next step to improve the lives of children living with CF.