Antiphospholipid syndrome (APS)

Hughes syndrome, sticky blood syndrome

What is antiphospholipid syndrome (APS)?

APS is an autoimmune condition that makes the blood stickier than normal, causing an increased risk of blood clots.

What causes APS?

Although there is no cure, the risk of developing blood clots can be reduced with treatment. To receive a diagnosis of APS, blood tests must be carried out by your GP.

What are the symptoms of APS?

Symptoms of APS include:

  • Fatigue
  • Headaches or migraines
  • Balance and mobility difficulties
  • Memory problems

Are you affected by Antiphospholipid syndrome (APS)?

If you’re affected by APS, The Brain Charity can support you.

We are the only charity in the UK to be here for every one of the more than 600 different neurological conditions in existence. Individually, many are rare, but combined, they affect 1 in 6 people.

We provide practical help on all aspects of living with antiphospholipid syndrome, emotional support such as counselling, phone befriending and group therapy and social activities to people with antiphospholipid syndrome from all over the UK from our centre in Liverpool.

Looking to talk to someone?

Phone us

Contact The Brain Charity now

Our friendly Information & Advice Officers are here to help. We endeavour to respond to all enquiries within 10 working days.

0800 008 6417

Looking to talk to someone?

  • This field is for validation purposes and should be left unchanged.

Caring for someone affected by Antiphospholipid syndrome (APS)

APS can affect people of all ages, including children and babies.

Living with APS requires some lifestyle changes: it is a good idea to encourage someone affected by this condition to eat a healthy balanced diet, exercise and stop smoking if applicable.

We support carers, friends and family too

Are you a carer for or relative of someone with antiphospholipid syndrome? It’s just as important for you to look after your own physical and mental wellbeing too.

The Brain Charity provides free support for carers, friends and family of people with any form of neurological condition, including antiphospholipid syndrome, from anywhere in the UK.

We also run an additional carers advocacy service for all carers in Liverpool, regardless of which type of condition the person they care for has.

You don’t need to be a formal or registered carer

We can help you even if you don’t view yourself as a formal carer or claim Carer’s Allowance. Find out some of the ways we support carers below.

Carer support from The Brain Charity in Liverpool Practical help

Support for carers

All The Brain Charity's services are free for carers and family members of people with neurological conditions too.
Brain Changer Arts Project Arts-based therapies

Activities for children and young people

Physiotherapy and occupational therapy for under-18s, delivered via fun dance and art and craft workshops.
View all

Other resources

The Brain Charity's library

The Brain Charity's library has a range of resources on APS

Visit our library to read Hughes Syndrome by Judy Graham, or search the catalogue online.

 

Support groups

Antiphospholipid Syndrome UK

Facebook group

Support groups at The Brain Charity

Are you interested in setting up an APS support group, or do you already run one? Email info@thebraincharity.org.uk to let us know.

Alternatively, you can check out our list of related support groups here.

Other charities

APS Support UK (charity offering support to anyone affected by antiphospholipid syndrome)

Phone: 0300 323 9943
Website: aps-support.org.uk