We support education, awareness and fundraising for critical research in APS Type 1.
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 2014, our community has grown to include patients, family members, loyal friends, caregivers, dedicated doctors, and scientists.