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

My grandson Thomas who is 13 has a very rare form of A T. It is a degenerative neurological condition which affects movement, creates chronic fatigue and needs full time support in school. Our whole family are already benefiting from the support from this small but very important charity. I would be so grateful for your kind sponsorship for this challenge.