Tel: 020 7188 8217
The Hughes Syndrome Foundation, a registered charity, aims to achieve earlier diagnosis and the best possible treatment for patients by:
- Informing doctors, nurses and GPs about Hughes/antiphospholipid syndrome.
- Raising awareness in the media and general public about Hughes/antiphospholipid syndrome.
- Offering support and understanding to anyone affected by the condition.
- Raising funds to provide support, education and research.
Last updated on 25/03/2015