The A-T Society is the small national charity funding and inspiring quality research for treatments and a cure for the disabling, life shortening genetic condition Ataxia-Telangiectasia.
The charity provides family support, advocacy and equipment to give children, young adults and their families the best quality of life possible. A-T is more than disabling; people with the condition have a high risk of developing cancer and lung disease and average life expectancy is just 26 years.
1 in 200 people carry the gene which can result in A-T, and you could be one of them. But most people, including doctors and health specialists have never heard of the condition. A-T Society asks you to help us raise awareness of A-T and bring a cure closer for every child diagnosed now and in the future. Thank you.