We fund international research in an effort to find life-improving therapies and a cure for ataxia-telangiectasia.
Producing the functional ATM protein that is missing within the cells of children with A-T
Screening thousands of compounds to find potential new drugs to help A-T
Discovering how the A-T protein works in brain cells to reveal ways to compensate or correct for the lack of the protein in children with A-T
Establishing and supporting the Global A-T Family Data Platform, a direct patient engagement website and data donation platform
Neuroimaging to reveal abnormal brain function in A-T
Conducting studies to improve the quality of care for people with A-T at the A-T Clinical Center at Johns Hopkins Hospital
We drive innovative research, develop potential therapies, organize scientific conferences and sponsor a multidisciplinary clinical center for ataxia-telangiectasia (A-T), a fatal genetic disease that attacks children, causing progressive loss of muscle control, cancer, and immune system problems.
Join the grassroots fundraising efforts with families and friends of the A-T Children’s Project.
Help fund critically needed A-T research. You can host any type of fundraising event, and we will help you every step of the way.
Join the A-T CureTeam as an official charity in several national marathon weekends!
You can take pride in the important difference your gift makes in the lives of families living with A-T.
