APS Type 1 Foundation

The APS Type 1 Foundation was started by a group of dedicated parents who were determined to ensure that their children received the best care possible and that no one should have to wait for a diagnosis or treatment for APS Type 1. Since our founding in 2012, our community has grown to include patients, family members, loyal friends, caregivers, dedicated doctors, and scientists. We support education, awareness and fundraising for critical research in APS Type 1.