Local branches

Greenwich and Blackheath Cystic Fibrosis Trust Fundraising Group

Contact: Rose DaileySacha Bright or Mary Bright

Since our formation in 2008 we have raised over £70,000 with a variety of local events including a fabulous Crimson Ball, an annual Quiz Night, Blackheath Christmas Shopping Evening and more recently a Bags and Baubles Extravaganza. We would warmly welcome anyone who wishes to join us and help to organise these and more events.

Kingston & Epsom Branch

Contact: kingstonepsomcftrust@hotmail.com

We are a long-standing fundraising group based in south west London. We all have a personal connection to CF and are extremely dedicated to raising as much as we can for the Cystic Fibrosis Trust. We aim to hold around 12 events a year (though it usually ends up more than this) and would welcome any newcomers from the area to our group. Our main events include a curry night, bridge nights, and Christmas events in October/November selling our famous reindeer food!

North East London Branch

Contact: Sue Lawrence

We have been going for over 30 years, and have a history of successful fundraising for the Cystic Fibrosis Trust. Although the original members have taken well deserved retirement, we all have a personal connection to cystic fibrosis; whether through our children or our friends' children. We would love to have some new volunteers to join our ranks, give us some new ideas and help grow our numbers and ensure that the group continues fundraising for the next 30 years!

Sixty-Five Roses Ball

There have been 10 Sixty-Five Roses Balls since the first one in 1998, raising almost £1m for the Trust.

The Committee are now thinking of a new format going forward. If you would like more information, would like to be on the committee, or just want to give some ideas, please contact Harriet on harrietvdl@btinternet.com.

Further information can be found on the Ball website at www.sixtyfiverosesball.org.uk.


Contact: Serena

Fundraising bought us together but we are more a group of good friends than a formal branch. Our favourite fundraising activity is arranging our legendary balls. We try to arrange a black tie dinner with auction, live music and all of the usual trimmings, every second year. We are out to enjoy our fundraising so Abba nights, Christmas stalls and race nights are also often on our list of things to join in with. We very much welcome new volunteers, we meet informally in a pub in Wokingham. If you'd like to come along you will be made most welcome.

Oxford Branch

Contact: Martin Powell

We are a very friendly, active and successful branch of the Cystic Fibrosis Trust who are passionate about fundraising and raising awareness. Our fundraising activities include a quiz night, live music gigs and collections, however, we welcome any ideas to boost our fundraising achievements further. We come from all walks of life, vary in ages but all share the common goal of helping in the fight against cystic fibrosis. We meet informally in Cumnor Hill once every four or five weeks. We very much welcome new supporters so please do come along to join us.

Headcorn Branch

Contact: Sandra Lee

Headcorn Branch is committed to raising awareness of cystic fibrosis in the local area. The branch organises quizzes and supports other Kent events. In the past the branch has organised some very successful Balls including an event at Leeds Castle.

Portsmouth Branch

Contact: Sue Kruk


We are a group of CF Supporters who meet and put on a few events each year. We have a casual/informal monthly meeting at various homes on Hayling Island, in Gosport, Locks Heath and Sarisbury Green.

If you live in the area and would like to get involved we would love to hear from you. 


Contact: Joe & Mary

This group doesn't meet formally but is made up of a local family organising and supporting a variety of events throughout the county. In the past events included musical concerts, garden parties, pub events, discos, race nights and lots more. 

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What is CF?

Cystic fibrosis, or CF, affects the lungs, digestive system and other organs, and there are over 10,600 people living with it in the UK.

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