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About AT
- About AT
  Ataxia-Telangiectasia or AT, is a rare and complex genetic disorder. It is often referred to as a ‘multi-system’ disorder because it affects a number of different systems within the body.
Living with AT
- Living with AT
  Find out all you need to know about the implications of the Coronavirus for those living with AT.
How we help
- How we help
  Our support team, Kay and Anne, are on hand 5 days a week to help and support families living with AT. From the shock of the initial diagnosis through to treatment and the challenges of everyday living, we can provide support, advice and advocacy for people with AT and their family, friends and carers. We also liaise with and offer advice to professionals.
  Kay and Anne can be contacted on 01582 760733.
Support us
- Support Us
  The AT Society is completely funded by grants and donations, so to keep doing what we do best, we need you to help us. Your support means we can continue to raise awareness. be there with emotional and practical assistance for new families, commission more medical research and provide a vital information resource for everyone involved with AT.
Shop
- Shop
  We have a wide range of gifts and fundraising merchandise in our online shop. Every single purchase helps to make a difference to children and their families living with AT.
Research
- Research
  Research funded and supported by the AT Society has done a lot to advance our understanding of AT and improve treatments. By bringing top scientists together and exploiting the latest advances in technology we will develop effective ways to treat and ultimately cure AT.
For Professionals
- For Professionals
  Ataxia-Telangiectasia (AT) is a very rare condition with an estimated 200 cases in the UK. Most professionals will have limited knowledge or be unaware of the condition when a person is referred to them.
About us
- About Us
  The AT Society exists to enable people with AT to make the most of the lives they have. We are unique in that we both support people with AT and fund research.

Call us on 01582 760733

About AT
- About AT
  Ataxia-Telangiectasia or AT, is a rare and complex genetic disorder. It is often referred to as a ‘multi-system’ disorder because it affects a number of different systems within the body.
Living with AT
- Living with AT
  Find out all you need to know about the implications of the Coronavirus for those living with AT.
How we help
- How we help
  Our support team, Kay and Anne, are on hand 5 days a week to help and support families living with AT. From the shock of the initial diagnosis through to treatment and the challenges of everyday living, we can provide support, advice and advocacy for people with AT and their family, friends and carers. We also liaise with and offer advice to professionals.
  Kay and Anne can be contacted on 01582 760733.
Support us
- Support Us
  The AT Society is completely funded by grants and donations, so to keep doing what we do best, we need you to help us. Your support means we can continue to raise awareness. be there with emotional and practical assistance for new families, commission more medical research and provide a vital information resource for everyone involved with AT.
Shop
- Shop
  We have a wide range of gifts and fundraising merchandise in our online shop. Every single purchase helps to make a difference to children and their families living with AT.
Research
- Research
  Research funded and supported by the AT Society has done a lot to advance our understanding of AT and improve treatments. By bringing top scientists together and exploiting the latest advances in technology we will develop effective ways to treat and ultimately cure AT.
For Professionals
- For Professionals
  Ataxia-Telangiectasia (AT) is a very rare condition with an estimated 200 cases in the UK. Most professionals will have limited knowledge or be unaware of the condition when a person is referred to them.
About us
- About Us
  The AT Society exists to enable people with AT to make the most of the lives they have. We are unique in that we both support people with AT and fund research.

Home / Give us a gift

Showing 1–12 of 14 results

A-T Activity Weekend
£800.00
A-T Support Helpline
£300.00
All-terrain powered wheelchair
£10,000.00
Amazon Fire 7 Tablet
£50.00
Counselling session
£50.00
Horse Riding lesson
£15.00
Lunch for a family attending A-T Clinic
£25.00
Month of Scientific Research
£5,000.00
New Family Information Pack
£5.00
Overnight stay for a family attending A-T Clinic
£100.00
Play Therapy Session for a child
£50.00
Specially adapted joy stick and computer keyboard
£175.00

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AT Society, Unit 54, Thrales End Business Centre, Thrales End Lane, Harpenden, Hertfordshire, AL5 3NS
Registered Charity No: 1105528

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+44 (0) 1582 760733

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