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Click here To enter the 1st World survey of APS patient symptoms

Anti Phospholipid Syndrome

This site is intended as a research resource for medical professionals, patients and families who wish to learn more about a little known lethal, yet treatable, blood disorder that causes hypercoagulation.

Early signs of this disease are often diagnosed as many different disorders before being correctly diagnosed. This inability to correctly diagnose is not due to any form of medical inefficiency, but is due to the disease only being recognised in the last 9 years, and it's ability to mimic the symptoms of a number of well known and documented diseases.

Even though I have a clinical diagnosis of APLS, wear an SOS Talisman bracelet and carry a medical fact card on me, in an emergency the Accident and Emergency doctors still insist on treating the possibly catastrophic events as a Migraine.

I hope this site will help to raise the awareness of many doctors and health care professionals, and give help and the comfort of understanding the problems to patients and their families.

Research into APS is still being completed at a number of hospitals and research centres worldwide. The information within this site has been collected from their sites and from weekly updates from Medscape.com

 

Search Intute: 

 

Search the Intute Internet Resource Catalogue

Funded by the JISC

The Intute database makes it possible to discover the best and most relevant resources in one easily accessible place. You can explore and discover trusted information, assured that it has been evaluated by specialists for its quality and relevance.

 

 

I would be interested to hear from patients and doctors who have experience of Anti Phospholipid Syndrome (APS) and its associated disorders.

If these pages have been of interest or help please e-mail me at Eddie@apls.tk with your comments and reasons for visiting the site, as this will help in assessing the need for updates.

Basic details on blood, clotting and the most common effects on the blood by APS

If you have found this site helpful and are a return visitor, you will notice that there are a number of new additions in the menu of diseases. These have been added as a direct result of the APLS Survey, where it was noticed that many of these diseases are shared by patients with APLS. I will continue to add new pages as I research them, and any help with links or information would be greatly appreciated.

Are you having trouble finding a doctor who knows about APS or a hospital that has a specialist Consultant for APS? Then you need:

www.specialistinfo.com, a site created not only for Doctors but also to provide invaluable information about Consultants to Healthcare Professionals, potential patients and their families.

As a registered user of this website, you will be able to see the scope of the site and obtain some useful information. However, full access is only provided to Subscribers.

Subscribers can see the full index of Consultants' special interests as well as Consultants' contact details and clinic times and even their clinic waiting times.
Subscription costs £99 per year per user. Discounts are available for multiple users, with a special fee for potential patients where access to the site can be obtained for £2.99 for 24 hours.
To subscribe, please contact Specialist Info:

Forum for patients and medical professionals APLSUK Yahoo Groups

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