Skip to main content Skip to navigation

hughes syndrome foundation

The charity supports the general public. Hughes Syndrome Foundation is a registered charity whose purpose is the advancement of health or the saving of lives. It delivers its work by providing advocacy, advice, or information. The charity is based in Hampshire and operates in England And Wales.


This page summarises publicly available information about the charity, including its activities, beneficiaries, and registration details, based on official records.

Email Charity

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.

Fundraising

See where Hughes Syndrome Foundation is active and find local fundraising opportunities.

Financial Information

Latest Income
£114,900
Latest Expenditure
£96,201

Financial Efficiency

Overall Efficiency 83.7%
% of expenditure going to programs (vs overhead)
Expenditure Ratio 83.7%
Expenditure as % of income

Financial Trend

Annual Returns

Financial YearIncomeExpenditureCharitable SpendingNet AssetsReservesStaff
2024£114,900£96,2010 / 6
2023£172,332£80,1480 / 8
2022£91,541£77,6920 / 8
2021£128,035£66,2740 / 15
2020£127,590£92,0200 / 13

Staff column shows: Employees / Volunteers