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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Celebrating Camden’s Progress: Finding His Voice, One Step at a Time
Camden has made remarkable progress in therapy, enhancing his balance, motor skills, and willingness to try new activities. Each small victory fills our family with pride.
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Meaningful Friendships Make Life Better
“Their kindness, thoughtfulness, and genuine care give us strength and fill our hearts with gratitude. Whether it’s a shared laugh, a thoughtful gift, or simply being…”
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Camden’s Visit to the Children’s Hospital of Colorado: A Journey of Hope and Hard Realities
“We now have expert advice to guide our local doctors, therapists, and schools in understanding and meeting Camden’s unique needs. We look forward…”
