Contact Us 

We'd love to hear from you. 
If you have a question about Hughes Syndrome (APS), our support for patients, or the work of the Hughes APS Trust, please get in touch.  
 
 
We are a small team, working part-time, so please bear with us if it takes a little longer to respond. 
 
We do read every message 
 
 

APS Champions 

You can become a Hughes APS Trust champion where you live. You might organise fundraising events, or help raise awareness locally, for example by distributing awareness raising leaflets. 
 
 
 
 
Join

Donate 

You can donate to help us reach as many medical professionals and patients as possible, raising awareness, and promoting early diagnosis. 
 
We rely entirely on donations to continue our life-changing work. 
 
Thank you for your support! 
 
 
Donate