The APS Foundation of America (APSFA) is a nonprofit organization dedicated to raising awareness, supporting research, providing education, and offering resources for individuals affected by Antiphospholipid Syndrome (APS), a serious autoimmune disorder associated with blood clots, recurrent pregnancy loss, stroke, and other health complications. Founded in 2005, APSFA serves patients, caregivers, healthcare professionals, and researchers through advocacy, support services, and public awareness initiatives.