Ataxia-Telangiectasia A-T Society

Ataxia-Telangiectasia in the UK

Welcome to the A-T Society Facebook page! This is a place for people with A-T, their friends, families, and anyone interested in the Society, to chat, share stories, news, pictures, plus plan and announce upcoming A-T Society events and fundraising ideas.

Ataxia-Telangiectaisa (“A-T”) 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 perhaps a more than normal number of infections. There is no cure or treatment available at present.

The A-T Society is a small national charity unique to the UK in the services it offers families. Since its foundation in 1989, the Society’s objective has been to alleviate the distress and suffering caused by A-T.

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

Join the A-T Society group to show your support!

For more information visit the website www. atsociety.org. uk or call the Society direct on + 44 (0 1582 760733
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A-T Society - Awareness Research Care
Reg. Charity No: 1105528