Say hello to the faces behind The Chris Aked Foundation 👋 Our team of trustees all had a personal connection to Chris, and our founder...

Nicola talks about how we've been able to support her family, and her work on developing The Little C Club: “I was diagnosed with...

There's one month to go until our annual CAF golf day! Join us on bank holiday Monday 29th August, at Royal Blackheath Golf Club. There...

Joshua was diagnosed with a rare genetic disease called SCID (Severe Combined Immune Deficiency) just before he turned two years old,...

Sign up to our newsletter for all the latest CAF news and events. You can join here (http://eepurl.com/gfkpbH) or from the footer of any...

We send out care packs to all new families referred to us, to hopefully bring a smile and brighten their day at such a difficult time. We...

Are you able to make a small monthly donation to help us support more families? We know times are tight for many right now, but if you...

Our second Festive 5k is now live! We are so excited to say you can sign up now and either get your first CAF medal or add to your...

Our Festive 5k is now live! We are so excited to say you can sign up here to take part in the first ever Chris Aked Foundation Festive...

A huge thank you to all the children who entered our Christmas card competition! We loved seeing your entries and judging was very close,...