Founded in 2010 by Christine Neitzke after her son Matt was diagnosed with Hodgkin’s Lymphoma Stage 3, The Dragonfly Foundation was created to fill a critical gap in pediatric cancer care—supporting the emotional, social, and essential needs of patients and their families. While excellent medical treatment is essential, the challenges of pediatric cancer extend beyond hospital walls.
At Dragonfly, we believe no family should face this journey alone. From the moment of diagnosis, we provide immediate support through care packages, hospital programs, and essential resources to ease the burdens of treatment. We foster a sense of community and connection through events, family outings, peer support and helping families combat the isolation that often accompanies a cancer diagnosis.
Our work does not end after treatment. The emotional and practical challenges of pediatric cancer often continue long after hospital stays, which is why we offer specialized programs, including hair-loss support and services to help families adjust to life beyond treatment. We recognize the importance of experiencing joy in the healing process. Through personalized gifts and uplifting experiences, we create moments of happiness that provide comfort and lasting memories.
Working hand-in-hand with hospitals and community organizations, Dragonfly provides holistic, unwavering support to pediatric cancer and bone marrow transplant patients and their families. We build a strong network that connects families to each other and the broader community, enhancing quality of life through programs, events, and resources designed to ease the profound burdens of illness.
While funding research is crucial, Dragonfly believes that providing compassionate, comprehensive support for these families is just as important. Our team equips partner hospitals with resources for the families to have the strength, courage, and joy they need to navigate this journey.
Today, Matt, our original Dragonfly, is cancer free.
Copyright 2024. All rights reserved.
