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Hughes APS Trust

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Hughes APS Trust

The Hughes APS Trust (formerly GHIC) was founded by expert doctors and researchers to educate, raise awareness, and fund vital research into Hughes Syndrome.

We rely entirely on donations to continue our life-changing work. Thank you for your support! We are proud to now be the Hughes APS Trust (formerly Graham Hughes International Charity, GHIC). Our new name marks an exciting new chapter — but our mission stays the same. We work to raise awareness, educate patients, doctors, and the wider public, and fund vital research to improve diagnosis, treatment, and care for people living with Hughes Syndrome (APS). Hughes Syndrome (APS) is a serious autoimmune disorder that can cause blood clots, pregnancy loss, strokes, and other life-threatening complications. Too often, it goes undiagnosed or misunderstood. Together, we can change that. We rely 100% on donations to power everything we do. Every gift you make helps to fund education, raise life-saving awareness, and drive research that brings hope to people with APS around the world. Please donate today and be part of building a better future for everyone affected by APS. Thank you for standing with us!

11/11/2025

We’re putting your questions to Dr Arvind Kaul, Consultant Rheumatologist and Chair of the Hughes APS Trust, for a special APS Q&A video coming this December.

If there’s something you’ve always wanted to ask about Antiphospholipid Syndrome (APS) — now’s your chance!

💬 Send us your question by 25 November via message or comment below.

Please note, we’re unable to give advice on individual treatments — you should always speak to your own doctor for personalised medical guidance.

30/10/2025

We recently shared the launch of our new website — and now we’re delighted to share a short welcome message from Professor Graham Hughes.
Many of you will know Professor Hughes as the doctor who first identified Hughes syndrome. His message perfectly captures the heart and purpose of our charity.
Watch below 👇

20/10/2025

Our New Website is Here! 🌐✨
We’re so excited to share our brand new Hughes APS Trust website with you!
It’s been designed to make finding information and support about Antiphospholipid Syndrome (APS) easier than ever — with clear explanations, helpful resources, and real stories from people living with APS.
We’d love for you to take a look, have a browse, and let us know what you think! 👇
🔗 www.hughesapstrust.org
Thank you to everyone who helped make this possible — we can’t wait for you to see it!

16/07/2025

👋 Hello everyone — and sorry for the delay in sharing this! We've been busy behind the scenes getting our new website ready, and we can’t wait to show you more very soon.

📢 Unfortunately, there isn’t a recording of the recent Ten Topics event — we know many of you were hoping to catch up afterwards.

However, we’re pleased to share some images from the day 📸, and we hope they offer a glimpse into the fantastic discussions and learning that took place.

📝 Good news — Professor Hughes will be writing a blog post summarising the key points from the event, which we’ll be sharing soon!

Looking ahead, we hope future events like this can be recorded, allowing us to share the insights more widely with our patients and supporters.

Thank you for your understanding 💜

Address

The Shard, TOG 24/25, 32 London Bridge Street
London
SE19SG

Opening Hours

Monday	9am - 5pm
Tuesday	9am - 5pm
Wednesday	9am - 5pm
Thursday	9am - 5pm
Friday	9am - 5pm

Telephone

+443008001234

Website

https://www.hughesapstrust.org/, https://www.justgiving.com/hughesapstrust

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Our Story

GHIC - is a global charity raising awareness, improving education and supporting all those affected by Hughes Syndrome (APS), in the UK and world wide.