APS Type 1 Foundation

Our Story

The APS Type 1 Foundation was founded in 2012 by dedicated parents committed to ensuring timely diagnosis and treatment for children with APS Type 1. This growing community includes patients, family members, caregivers, and medical professionals, all united in their mission to support education, awareness, and critical research.

Impact

Since its inception, the foundation has hosted five International Symposia and one Global Scientific Summit, awarded over $550,000 in research grants, and established the world’s first web-based registry for APS Type 1 patients, currently enrolling 125 individuals.

Why Donate?

Your contributions empower the APS Type 1 Foundation to unite and support a global community, driving awareness, education, and groundbreaking research that transforms lives affected by this rare autoimmune disorder.

Get Involved

Join the fight against APS Type 1 by donating cryptocurrency or cash today. Your support is crucial in advancing research and improving the lives of those impacted by this condition.