Welcome to the National Organization for Disorders of the Corpus Callosum!
Thank you for visiting our new website. Content is being added frequently, so please check back often.
Our mission is "to enhance the quality of life and promote opportunities for individuals with disorders of the corpus callosum, and raise the profile, understanding and acceptance of these disorders through research, education, advocacy and networking."
With the assistance of many wonderful volunteers and donors, we organize and facilitate family gatherings both nationally and regionally. Families with individuals diagnosed with a disorder of the corpus callosum enjoy the tremendous support they receive from these gatherings.
We offer free educational and other resource materials right here on our website. Please explore it and watch for updates, as this new site is in the process of adding useful and informative content related to Disorders of the Corpus Callosum. Also, be sure to watch for our new Membership and Family Partnership programs! Signup forms coming soon to this site.
Our support comes entirely through donations from our members and other individuals, foundations and corporations. We are currently featuring a special opportunity to give a $20 or greater donation, and receive as our thanks a wonderful and sought after book for children who have a disorder of the corpus callosum known as Agenesis of the Corpus Callosum (ACC).
ACC and Me
Illustrated Children’s Book
By Dr. Kathryn Schilmoeller and Dr. Lynn K. Paul
This wonderful book explains ACC from a child’s perspective in a simple, informative way. A great book to share with your child’s friends, family and classmates. Get your copy for a minimum $20 donation or greater!