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Hughes Syndrome Foundation and MuchLoved - creating memorial websites in partnership

Hughes Syndrome Foundation
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  Welcome to the website of the Hughes Syndrome Foundation. We are a UK registered charity dedicated to promoting awareness and funding research into Hughes Syndrome which is also known medically as the antiphospholipid syndrome (APS). Our website provides information about the charity and all aspects of Hughes Syndrome for patients, doctors and supporters.

Hughes Syndrome is an autoimmune disorder which can present many clinical features, some of which can be life threatening, including strokes and thrombosis, and it can also be the cause of recurrent miscarriage. The good news is that, once diagnosed, Hughes Syndrome is potentially treatable; the bad news is that, as the condition is relatively new, it often goes undetected or misdiagnosed. With your help we hope to raise the profile of Hughes Syndrome so that we can discover more about its causes, prevalence and treatment.
   

Christmas Wishes to You Book your place at the National Patients' Day on 16th May 2012

Christmas Wishes to You Take part in the historic 2012 British 10K Run on 8th July - just before the Olympics.

Blogs, questions and more from the Hughes Syndrome community


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© 2011 Hughes Syndrome Foundation, Registered Charity No 1138116
Conybeare House, Guy's Hospital, London, SE1 9RT
telephone: 0207 188 8217 email: info@hughes-syndrome.org