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The A-T Society is the only charity supporting children and young people with Ataxia-Telangiectasia (A-T) 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.

Ataxia telangiectasia (A-T) is rare condition that affects the nervous system, the immune system, and many other parts of the body.

The condition is typically characterised by cerebellar ataxia (uncoordinated muscle movements), oculomotor apraxia, telangiectasia, choreoathetosis (uncontrollable movements of the limbs), a weakened immune system with frequent infections, and an increased risk of cancers such as leukaemia and lymphoma.

A-T is caused by changes in the ATM gene and is inherited disease from both parents.