A-T Society (Ataxia-Telangiectasia Society)
Charity information
A-T Society (Ataxia-Telangiectasia Society)
The A-T Society (Ataxia-Telangiectasia Society) is the only UK charity providing family support and medical research into treatments and a cure for Ataxia-Telangiectasia.
Founded 1989
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Mission statement
Our vision is:
A world where no one need suffer from the devastating effects of A-T
Our mission is:
To improve quality of life and quality of care for people living with A-T while actively promoting research to lengthen lives and ultimately bring about a cure.
We do this by
• Providing information and support to meet the challenges of living with A-T
• Working to achieve better, more coordinated health and social care services
• Promoting and funding high quality A-T research
• Speaking out to ensure that the voices of people affected by A-T are heard
• Raising awareness of A-T and gathering supporters and resources to help achieve our vision -
Aims
A-T Society (Ataxia-Telangiectasia Society) aims to:
- To raise awareness of Ataxia-Telangiectasia within the general population and the medical community.
- Family support for children, young people and their families living with Ataxia-Telangiectasia.
- To fund research towards treatments and a cure for Ataxia-Telangiectasia - improving quality of life and quality of care.
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Overview
Established: June 1989
Registered Charity Number: 1105528
Board members: 12
Full time staff: 3
Part time staff: 1
Volunteers: 10
Phone number: 01582 760733
Address: Rothamsted Harpenden Hertfordshire AL5 2JQ
View charity accounts on the Charity Commission website
