Welcome to The Cure for Camden!
This page follows the journey of our brave little boy, Camden, who was diagnosed with SYNGAP1, a rare genetic disorder affecting brain development. We’re here to raise awareness, share our experiences, and connect with a community dedicated to finding a cure. Join us as we navigate the highs and lows, celebrate Camden’s progress, and advocate for research and resources that will make a difference. Your support is invaluable—please consider donating to the Syngap Research Fund (SRF) to help fund crucial research that brings us closer to a cure. Thank you for being part of Camden’s story and supporting our mission!
Recent Posts
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Climbing Together: Hope, Community, and Momentum at the Cure SYNGAP1 Conference
We were surrounded by people who simply understood. That sense of belonging, paired with real scientific progress, reminded us we are not walking this path alone.
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Camden’s Year of Resilience: A Letter from the Heart
This letter is for Camden, a testament to his incredible spirit and the journey we’ve embarked on together.
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A Promise Made Closer to Home: The Impact of Children’s Mercy in Wichita
This new clinic is not just about convenience—it’s about making families feel seen, valued, and cared for, right in their own community.
