If you have recently been diagnosed with Hughes/antiphospholipid syndrome, you may feel overwhelmed and isolated. This section aims to help you learn about your diagnosis, how to find support and feel more in control of your health
Hughes/antiphospholipid syndrome can cause a myriad of different symptoms both low-grade, such as headaches, and also serious conditions as a result of blood clots. It is not necessary to have all the symptoms to be diagnosed with Hughes/antiphospholipid syndrome.
...achieve earlier diagnosis and the best possible treatment for patients by:
Our charity exists to support patients with APS/Hughes syndrome. Many clinicians now only use APS to describe the condition, and patients need to be aware of this fact when they visit their GP or specialist.
© 2016 The Hughes Syndrome Foundation. Registered Charity Number 1138116. A company limited by guarantee registered in England 7268671.