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

In 2008 my son Kaesin was born with C-ACC. I was a scared mother, with very little support, and no knowledge of ACC. Thanks to prayers, NDOCC, therapy, specialists, and a great family physician(who asked his entire staff to research ACC), Kaesin is doing well!Thank you to the NDOCC, who has provided information and support for my family, and others who are affected by this rare disorder!

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