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.
Find out all you need to know about the implications of the Coronavirus for those living with AT.
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.
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.
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 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.
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.
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.
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.
Find out all you need to know about the implications of the Coronavirus for those living with AT.
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.
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.
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 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.
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.
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.
We know many families were hoping for encouraging news from the recent Phase 3 trial of eDSP. Sadly, Quince Therapeutics has announced that the treatment did not show the improvement researchers were looking for, and as a result, they will be stopping further development of this therapy.
Please click below to read Quince’s full statement.
