Antiphospholipid Antibody Syndrome or Hughes Syndrome

• 3/23/2008 - Volume 8 of Our Newsletter, "Antiphospho...What?" is available for download!

Volume 8 of Our Newsletter, "Antiphospho...What?" is available for download!

The newest installment of our quarterly newsletter, "Antiphospho...What??" is available for download at this link: 
http://www.apsfa.org/docs/APSFAVol8WinSpr2008.pdf

The next volume will be coming out in May, 2008.
 
Thank you to those people who submitted articles. If you have submitted an article and we have not used it yet, we will be using it in the near future.
 
We are in need of patient stories (esp about Men and Teens or Children), recipes, poems, related book reviews, and anything else you think would be of interest for upcoming newsletters. Please submit articles to the following email address:
articles@apsfa.org


If you have an idea and are not sure if it would fit, please feel free to contact us through our contact page on the website, or email us using the email add or email us using the email address below. We are open to any suggestions.
 
Please remember to check our website for any changes at the following link:
http://www.apsfa.org/new.htm
 
Thank you for your continued support.


Keywords: APSFA, APS Foundation, antiphospholipid antibody syndrome, lupus, stroke, dvt, pe, thrombosis, clot, migraine, hughes syndrome, miscarriage, america, usa, anticoagulant, heart attack, APS

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About Me

The APS Foundation of America, Inc. is the only United States nonprofit health agency dedicated to bringing national awareness to Antiphospholipid Antibody 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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