Helen Scott
Lead On for the AT Society
Fundraising for AT Society
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.
* Charities pay a small fee for our service. Find out how much it is and what we do for it.