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Ataxia-Telangiectasia (“A-T”) is a rare, genetic, neurodegenerative disease which affects many parts of the body causing severe disability. The A-T Society is a charity, established in 1989, committed to helping, supporting and advising families affected by A-T. On this website you can find out about A-T and about support for families affected by it. You are free to download our leaflets and newsletters and may contact us directly. You will also find information about the latest research into A-T. And if you want to help us, you will find out how you can. News and Events About this website This website is updated every three months. We welcome your comments and feedback – contact the A-T Society Copyright belongs to the A-T Society. |
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