The Ataxia-Telangiectasia Society
Also known as: The a-T Society
Ataxia Telangiectasia (AT) is a progressive genetic condition which from early childhood causes increasingly severe disability, and shortens lives. The AT Society is dedicated to improving quality of life and quality of care for people living with AT while actively promoting research to lengthen lives and ultimately bring about a cure.
Activities & Mission
Ataxia Telangiectasia (AT) is a progressive genetic condition which from early childhood causes increasingly severe disability, and shortens lives. The AT Society is dedicated to improving quality of life and quality of care for people living with AT while actively promoting research to lengthen lives and ultimately bring about a cure.
Areas of Operation
Where this charity is registered to operate, as self-declared to the Charity Commission. These are regulatory classifications, not a list of active programmes, and don't necessarily indicate fundraising activity in each location.
Country
Region
Financial Information
Financial Efficiency
Latest Financial Breakdown
Income Sources
Expenditure Categories
Financial Trend
Annual Returns
As filed with the Charity Commission for England and Wales. Most recent filing covers the financial year ending 2024.
| Financial Year | Income | Expenditure | Charitable Spending | Net Assets | Reserves | Staff |
|---|---|---|---|---|---|---|
| 2024 | £657,491 | £571,908 | £426,554 | £485,316 | £404,744 | 9 / 40 |
| 2023 | £478,337 | £662,593 | 0 / 30 | |||
| 2022 | £429,145 | £481,406 | 0 / 10 | |||
| 2021 | £368,340 | £500,634 | 0 / 10 | |||
| 2020 | £320,758 | £505,594 | 0 / 1 |
Staff column shows: Employees / Volunteers
Frequently asked questions about The Ataxia-Telangiectasia Society
What does The Ataxia-Telangiectasia Society do?
Ataxia Telangiectasia (AT) is a progressive genetic condition which from early childhood causes increasingly severe disability, and shortens lives. The AT Society is dedicated to improving quality of life and quality of care for people living with AT while actively promoting research to lengthen lives and ultimately bring about a cure.
How much income did The Ataxia-Telangiectasia Society report in 2024?
The Ataxia-Telangiectasia Society reported total income of £657k and reported expenditure of £572k for the financial year ending 2024, based on the most recent annual return filed with the Charity Commission.
When was The Ataxia-Telangiectasia Society registered as a charity?
The Ataxia-Telangiectasia Society was registered with the Charity Commission for England and Wales on 18 August 2004 as charity number 1105528. It has been registered for 22 years.
Who runs The Ataxia-Telangiectasia Society?
The Ataxia-Telangiectasia Society is governed by a board of 8 trustees. The chair of trustees is Rachel Poupard. Trustees are legally responsible for the charity's governance and are listed in full on its profile.
Where does The Ataxia-Telangiectasia Society operate?
The Ataxia-Telangiectasia Society operates across 3 areas: Northern Ireland, Scotland and England And Wales.
Is The Ataxia-Telangiectasia Society a registered charity?
Yes — The Ataxia-Telangiectasia Society is a registered charity in England and Wales, charity number 1105528.
Details
Thrales End Business Centre
Thrales End Lane
Harpenden
Herts
AL5 3NS
Registry Information
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Also Known As
- The a-T Society
Data & trust
- Register data refreshed
- 30 July 2026
- Methodology
- How metrics are calculated