The APS Foundation of America, Inc. (APSFA) is the only US nonprofit health agency dedicated to bringing national awareness to Antiphospholipid Syndrome (APS), the major cause of multiple miscarriages, thrombosis, young strokes & heart attacks. We are a volunteer run, community based 501(c)3 non-profit Public Charity organization & is dedicated to fostering & facilitating joint efforts in the areas of education, support, public awareness, research & patient services. The APSFA’s Medical Advisory Team includes nationally & internationally recognized experts on APS.
Are you looking for Support for Antiphospholipid Antibody Syndrome, APS, APLS, APLA, Hughes Syndrome, or Sticky Blood?
Well you've come to the right place! This is an closed forum for people who have Antiphospholipid Syndrome.
This pamphlet is a layman’s terms summary of Antiphospholipid Syndrome (APS). It covers such topics as diagnosis, symptoms, treatment, and coping. It is meant for patients newly diagnosed, however would also be good for informing friends and family