Ataxia-Telangiectasia Society

The A-T Society was established in 1989 and is committed to helping, supporting and advising families affected by A-T particularly at the very difficult time of diagnosis. The objective of the Society is to alleviate the distress and suffering that A-T causes by working to improve quality of life now and in the future. We do this through funding research, supporting families, working to improve clinical management, raising awareness. Amongst other things we provide information on A-T, organise an annual Family Day, make grants for equipment such as computers, wheelchairs etc.