|
The NODCC is a community of individuals, parents, their families and friends looking to connect and support one another through times of uncertainty and moments of triumph. If you, your child or someone you love has been diagnosed with a callosal disorder you may be experiencing a variety of emotions, and you’ve probably got questions—lots of them. Our members come from all around the world and they share a common desire to discuss, learn and ask for help on a wide variety of topics. Our community is committed to fostering understanding about disorders of the corpus callosum and providing forums for positive relationship building and the promotion of open communication and dialogue.
Our Stories This unique section is as an electronic book, which will eventually contain hundreds of pages of individuals’ and families’ personal stories about living with a callosal disorder. These anonymous stories are categorized by condition, gender and birth date.
Family Partnership Program The Family Partnership Program (FPP) is designed to connect individuals with DCC and their family members, with other people who have similar concerns. This Program includes the
FPP
Networking
Center , the FPP Resource Families and the FPP Regional Communities.
Discussion Board Here is a great place for sharing experiences and the exchange of ideas relative to living with a disorder of the corpus callosum. Simply leave a message on the board and check back to see response messages. This forum is easy to use, doesn’t clutter email, and is accessible 24/7.
Adult Community We invite adults diagnosed with a disorder of the corpus callosum to join this discussion forum featuring independent living topics and opportunities for socialization and connection.
|
