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Registered charity · No. 1138116Charitable companyWhite Hart Lane

Hughes Syndrome Foundation

Hughes Syndrome Foundation is a registered charity in England & Wales working in the advancement of health or saving of lives, based in White Hart Lane.

Quick answer

Hughes Syndrome Foundation is a registered charity (number 1138116) on the Charity Commission for England and Wales register, so it is a legitimate, regulator-overseen organisation. It is registered for: the advancement of health or saving of lives. Its latest reported income was £114,900 (year ending 2024-12-31). CharityCompare shows its official register record below; a Clarity Score is added automatically once detailed filing history is available.

Key facts

Registered charity number
1138116
Status
Registered (active)
Charity type
Charitable company
Location
White Hart Lane
Latest income (year ending 2024-12-31)
£114,900

What the charity does

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.

Registered causes

The Advancement Of Health Or Saving Of Lives

Why there's no Clarity Score yet

The Clarity Score is computed from full financial filing history. Hughes Syndrome Foundation is on the official register but outside the detailed-filing group we currently score (or awaiting its first filings), so we show its official register record instead of a rating. Its score appears automatically once enough filing data exists — never by payment. How scoring works

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Frequently asked questions

Is Hughes Syndrome Foundation a legitimate charity?
Yes. Hughes Syndrome Foundation is a registered charity (number 1138116) regulated by the Charity Commission for England and Wales. You can verify it on the official register.
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 can I donate to Hughes Syndrome Foundation?
Hughes Syndrome Foundation's website is http://www.aps-support.org.uk — donate there directly so the charity receives the full amount. CharityCompare never takes a commission on donations.

Source: Charity Commission for England and Wales register extract dated 2026-07-18, used under the Open Government Licence v3.0. Always verify current details on the official register entry.