How we can help
The A-T Society is here to support anyone affected by Ataxia-Telangiectasia (A-T) or a variant of A-T and the people who care for them.
One of the Society's most important aims is to fund and promote research to find better treatments and ultimately a 'cure' for A-T.
However the quality of life for children and adults who have A-T in the 'here and now' is just as important.
We have two Family Support Officers with over fifteen years experience in working with A-T families and within health and social care; Kay Atkins (Family Support Manager) and Anne Murray (Family Support Co-ordinator). We are able to offer support, advice and advocacy for people with A-T and their family, friends and carers. We also liaise with and offer advice to professionals.
You can contact Kay and Anne on 01582 760733, or email Support
(Normal working hours are Mon-Fri: 8.30am - 4.30pm, please do leave a message out of these times). Please note that all communication is treated in complete confidence.