We support people with AT & fund research to help them live well and find a cure

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Ataxia-Telangiectasia (“AT”) is a complex genetic disease which affects many parts of the body and causes severe disability. The symptoms include lack of balance, slurred speech and more than normal infections.

The AT Society is a small national charity unique to the UK in the services it offers families. The Society’s objective has been to alleviate the distress and suffering caused by AT.

The AT Society provides support services for families, funds research and specialist AT clinics, and helps raise awareness.