The APS Type 1 Foundation exists to drive research to improve the lives of people with this rare disease, and ultimately find a cure. We support education, awareness and fundraising for critical research in APS Type 1.

Our patients, doctors, and families at the 2023 Symposium in Washington, DC

Our Work

All of our activities are focused on connecting patients and families to the best care possible, providing clinician-scientists with opportunities to connect with patients and share their work, while driving research forward by awarding significant grants.

Our patients and families at the 2017 Symposium in Stony Brook, NY.