Welcome to the Official site of the APS Foundation of America, Inc!

Founded in 2005, The APS Foundation of America, Inc. (APSFA) is the leading United States nonprofit health agency dedicated to bringing national awareness to Antiphospholipid Syndrome (APS), the major cause of multiple miscarriages, thrombosis, young strokes and heart attacks. We are a volunteer run, community based 501(c)3 non-profit Public Charity organization and is dedicated to fostering and facilitating joint efforts in the areas of education, support, public awareness, research and patient services.


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Antiphospholipid Syndrome

What is Antiphospholipid Syndrome (APS)? APS is associated with recurrent clotting events (thrombosis) including premature stroke, repeated miscarriages, phlebitis, venous thrombosis (clot in the vein) and pulmonary thromboembolism (blockage of an artery found in the lung due to a clot that has traveled from a vein). It is also associated with low platelet or blood elements that prevent bleeding. Recently, however, even more disease states have been linked with APL including premature heart attack, migraine headaches, various cardiac valvular abnormalities, skin lesions, abnormal movement/chorea, diseases that mimic multiple sclerosis, vascular diseases of the eye that can lead to visual loss and blindness.

APS is an autoimmune disorder in which the body recognizes certain normal components of blood and/or cell membranes as foreign substances and produces antibodies against them. There are two known forms of APS. APS may occur in people with systemic lupus erythematosus, other autoimmune disease, or in otherwise healthy individuals. Sadly, when most people hear about APS and it being referred to as autoimmune disease, they incorrectly confuse the terms autoimmune with acquired immune deficiency syndrome (AIDS); or they think this is a form of cancer.

Lack of knowledge and awareness results in needless suffering for persons with APS. Misdiagnosis and / or delayed diagnosis usually result in damage to vital organs. The APS Foundation of America, Inc's vision is to bring national attention to APS as a common factor in multiple miscarriages, thrombosis, young strokes and heart attacks is vital in order to bring a joint effort to research, funding, early detection, and eventually, prevention and cure for APS.

APS is also referred to as APLS or APLA in the United States and formerly as Hughes Syndrome or Sticky Blood in the UK.



Do you have Lupus Anticoagulants? Join a Donor Program! Make a Difference!

George King Bio-Medical, Inc is searching for persons who have been diagnosed with Antiphospholipid Antibody Syndrome (APS)

George King Bio-Medical, Inc. has been a leader in the clinical community since 1973. Our plasmas are used for patient testing and research projects in laboratories worldwide. We supply most of the renowned and respected laboratories in the United States. We also work closely with leading pharmaceutical and biotech companies who develop products that are used in testing people with Antiphospholipid Syndrome (APS).

If you would like more information on how you can donate your plasma to George King Bio-Medical, Inc please visit this page: Lupus Anticoagulants?

For more information about George King Bio-Medical, Inc: http://www.kingbiomed.com



Are You on Warfarin or Coumadin? Check out INR Tracker!

INR Tracker was founded in April 2012 as the definitive personal health management tool designed for Warfarin patients. With INR Tracker, patients can generate easy to read reports to help them and their doctor figure out what may be causing fluctuations in their Warfarin therapy. INR Tracker also provides easy to use tools to help you figure out what your INR level means, what foods have vitamin k and to help you understand the symptoms of blood clots. INR Tracker was founded by a couple affected by a blood clot.

For more information: http://www.inrtracker.com



If You Have Antiphospholipid Syndrome (APS) And Lupus, You May Qualify For A Research Study

The Paisley Study is a research study that is evaluating an oral investigational drug for people with moderate to severe systemic lupus erythematosus (SLE). Qualified participants must be on stable anticoagulant therapy as long as APS is not the sole or predominant feature of their SLE.

Visit PaisleyStudy.com to learn more today.



The Faces of APS

The service we used to display the "Faces of APS" has closed. We were not given any warning and have lost all of the photos we collected from APS patients and their families. We are in the process of finding another slideshow service. In the meantime, we need to collect photos of APS patients to display on the site. If you would like your picture to be included please contact us via the website, support forum, Facebook, or Twitter for details on where to send the photos. We appreciate your assistance, patience, and continued support!

Click here to see the Faces of APS (on our photo album site) that we have collected so far. We hope to have a slideshow available again soon!


Women are more likely than men to be affected by APS. Some estimates say that 75% to 90% of those affected are women. For example, it has been estimated by some doctors that one third of all of young strokes (defined as under the age of 50) are due to APS.

In obstetrics it is estimated by some doctors that up to 25% of all women with 2 or more spontaneous miscarriages have APS. Some doctors believe that 1 in 5 of all Deep Vein Thrombosis (DVT), Pulmonary Embolism (PE), and even worse, amputations are due to APS. And it is believed that 40-50% of patients with Lupus also have APS. Still, with these statistics, APS rarely is discussed as a women's health issue and is misdiagnosed often. Therefore the total number of people affected and true statistics are unknown really.


Page last update: 05/30/2018

The APS Foundation of America, Inc. website and forums are both volunteer run and funded by donations to the APSFA.

Website hosted by Dreamhost. Website created and maintained by Heidi P.

DISCLAIMER: APS Foundation of America, Inc. website is not intended to replace standard doctor-patient visits, physical examination, and medical testing. Information given to members is only an opinion. All information should be confirmed with your personal doctor. Always seek the advice of a trained physician in person before seeking any new treatment regarding your medical diagnosis or condition. Any information received from APS Foundation of America, Inc. website is not intended to diagnose, treat, or cure. This site is for informational purposes only. Please note that we will be listing all donor or purchaser's names on the Donor page of our foundation site. If you do not want your name listed, please contact us to opt out. If you think you may have a medical emergency, call your doctor or 911 immediately.

APS Foundation of America, Inc. will be building a database with your email, name and address information for future mailings. Your information will be kept confidential and not sold to any third parties. You may opt out at anytime by emailing us.

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