The AT Society is the only charity supporting children and young people with ataxia telangiectasia (AT) and funds research to find a cure. We offer families an essential lifeline; advising and support through the many challenges they face. Life expectancy is currently just 26.

I am doing this event to raise as much money as possible for the charity whilst at the same time trying to raise awareness of this debilitating condition. I had not heard of it myself until my step-mother was diagnosed with it a few years ago. Please give whatever you can. Your donation makes a real difference.