2017 APS Awareness Month - APS Foundation of America, Inc.

APS Foundation of America, Inc.

Founded in 2005, the APS Foundation of America, Inc. (APSFA) is the only 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. The APSFA's Medical Advisory Team includes nationally & internationally recognized experts on Antiphospholipid Antibody Syndrome. Our URL is http://www.apsfa.org

Day 16

APS Awareness Month ~ Day 16: Whether you are a newly diagnosed APS patient or not, you will likely have felt overwhelmed, like no one understands. You may find comfort in joining an online #support community where you can connect with other #APS patients and share your experiences. You will find that you are not alone. We offer a private support group here on Facebook. the link is: http://www.facebook.com/groups/APSFriendsandFamily/ Please join us for your support needs!! Also, please share today's graphic with the hashtags #GOBURGUNDY and #APSAWARENESS. — meeting other APS patients.

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