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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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.
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The Weight of It All: Fighting for Camden’s Future
“If you’ve ever wondered how you can help, this is it. Stand with us. Speak out. Because Camden—and so many kids like him—deserve better than this.”
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From Christmas Challenges to Birthday Joy: What Camden Taught Us
“This time, we focused on Camden—his interests, his joy—and let go of any preconceived notions…”
