The A-T Society is a non-profit organization dedicated to supporting individuals affected by Ataxia-Telangiectasia (A-T), a rare genetic disorder. The society focuses on raising awareness, funding research, and providing resources for families dealing with the challenges of A-T. In addition to research funding, the A-T Society offers educational materials and support networks for patients and caregivers. They aim to improve the quality of life for those impacted by A-T and work towards finding effective treatments and a potential cure for this condition.