When I was 20 weeks pregnant, my doctor recommended an amniocentesis so we could find out what was causing concerns during my pregnancy. They took amniotic fluid for testing, and that's when my husband and I learned our daughter had a rare genetic disorder called Fanconi anemia (FA). We found out that we were both carriers, something we had never known.
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Zac Dockins
Development Coordinator
Growing up in North Idaho, Zac has worked with cancer-related organizations from a young age. His passion for helping others took root as he began volunteering at hospitals and nonprofits.
Zac earned a BA in Nonprofit Management, Psychology, and Marketing from Boise State University in 2021, followed by an MBA in Strategic Management from the University of North Texas in 2024. Before joining FCF, he gained experience in higher education as well as Dutch Bros Coffee.
In 2025, Zac joined FCF as a Development Coordinator, bringing his strategic thinking and dedication to fundraising and donor relations. With a strong commitment to fostering community engagement and making a meaningful impact, he looks forward to helping those affected by Fanconi anemia. When he’s not working, Zac enjoys crocheting, hiking, traveling, listening to music, and spending quality time with his cat, Maggie!
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The Family Retreat offers families a break from appointments, treatment decisions and everyday responsibilities. Children can try new activities and grow in confidence while caregivers learn, share practical support and connect with one another. The relationships formed at camp often continue long after everyone goes home.
By Cecilia Córdoba, mother of Agustina Milagros Kaucic When my daughter Agustina was 2 and a half years old, our lives changed forever. It was very difficult to reach a diagnosis. And when we finally received it, it was devastating....