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To help raise funds to advance research and education regarding Agenesis of the Corpus Callosum

Born with a partial Corpus Callosum, Colin grew up in a world that really didn't understand his challenges. The obstacles were many especially when dealing with processing, abstract concepts and social learning. Though the critical years were early on, sharing information at the national conference, and participation in research studies, gave Colin, parents and educators needed insight into his thoughts, perceptions and behaviors. Thankfully, because of the NODCC, he went from saying " the toe climber thing " ... aka... a chain link fence, to being an articulate, confident 18 year old college student. Now, Colin is not shy about sharing who he is, and what he needs. Every day, because of advancments in testing, more and more children are being diagnosed with Agenesis of the Corpus Callosum ( AgCC). Please join Colin and his family and help support the worthy work done at the NODCC.

With thanks,

Colin and his family

Updates and Donor Comments

  1. Carole RossCarole Ross 09/16/2011 at 09:30 AM ET
    You're such a valuable person, truly inspiring!

Organization Information

  • Summary

    The NODCC is the only national organization serving people with a disorder of the corpus callosum (DCC) and their families.
  • Reports

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