Hughes Syndrome Foundation
Also known as: Aps Support UK
We aim to achieve earlier diagnosis and better treatment for people with antiphospholipid syndrome (APS).We support anyone affected by APS; provide education and awareness within the medical profession; raise awareness of APS in the general public and raise funds to provide support, education and research.
Activities & Mission
We aim to achieve earlier diagnosis and better treatment for people with antiphospholipid syndrome (APS).We support anyone affected by APS; provide education and awareness within the medical profession; raise awareness of APS in the general public and raise funds to provide support, education and research.
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.
Region
Financial Information
Financial Efficiency
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 | £114,900 | £96,201 | 0 / 6 | |||
| 2023 | £172,332 | £80,148 | 0 / 8 | |||
| 2022 | £91,541 | £77,692 | 0 / 8 | |||
| 2021 | £128,035 | £66,274 | 0 / 15 | |||
| 2020 | £127,590 | £92,020 | 0 / 13 |
Staff column shows: Employees / Volunteers
Frequently asked questions about Hughes Syndrome Foundation
What does Hughes Syndrome Foundation do?
We aim to achieve earlier diagnosis and better treatment for people with antiphospholipid syndrome (APS).We support anyone affected by APS; provide education and awareness within the medical profession; raise awareness of APS in the general public and raise funds to provide support, education and research.
How much income did Hughes Syndrome Foundation report in 2024?
Hughes Syndrome Foundation reported total income of £115k and reported expenditure of £96k for the financial year ending 2024, based on the most recent annual return filed with the Charity Commission.
When was Hughes Syndrome Foundation registered as a charity?
Hughes Syndrome Foundation was registered with the Charity Commission for England and Wales on 17 September 2010 as charity number 1138116. It has been registered for 16 years.
Who runs Hughes Syndrome Foundation?
Hughes Syndrome Foundation is governed by a board of 7 trustees. The chair of trustees is BARONESS ESTELLE MORRIS. Trustees are legally responsible for the charity's governance and are listed in full on its profile.
Where does Hughes Syndrome Foundation operate?
Hughes Syndrome Foundation operates in England And Wales, as recorded in its Charity Commission filing.
Is Hughes Syndrome Foundation a registered charity?
Yes — Hughes Syndrome Foundation is a registered charity in England and Wales, charity number 1138116.
Details
WHITE HART LANE
BASINGSTOKE
HAMPSHIRE
RG21 4AF
Registry Information
Is this your charity?
Add your logo, photos and tell the story behind the numbers in your own words. Free for our first 50 launch partners.
Claim this listing Learn more about premium profilesOther notable Charity and VCS support charities
Major UK charities in the same primary sector, drawn from the curated priority cohort.
Trustees
Sectors & Classifications
Also Known As
- Aps Support UK
Data & trust
- Register data refreshed
- 14 May 2026
- Methodology
- How metrics are calculated