The 2022 Inaugural Global Scientific Summit on APS Type 1, Massey College, University of Toronto (Photo by Nick Wons)

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 2012, our community has grown to include patients, family members, loyal friends, caregivers, dedicated doctors, and scientists.

We have hosted four international symposia bringing families and researchers together.  In 2022, we hosted our inaugural internet research summit and building a global research network on APS Type 1.

Our Mission in Action