The APS Foundation of America (APSFA) is a volunteer-run nonprofit organization dedicated to increasing awareness, education, research, support, and patient services related to Antiphospholipid Syndrome (APS). Founded in 2005, APSFA provides educational resources to help patients, families, caregivers, and the general community better understand APS, including information about symptoms, diagnosis, treatment, prevention, and related health concerns. The organization also supports research efforts, shares medical and patient resources, maintains a doctor information directory, publishes newsletters, and provides an online community for people affected by APS. Through donations, fundraising programs, educational materials, awareness initiatives, and community involvement, APSFA works to bring greater national attention to APS and support individuals and families affected by the condition.