National Organization for Disorder of the Corpus Callosum Family Partnership Program

The National Organization for Disorders of the Corpus Callosum (NODCC) Family Partnership Program maintains a database of families and adult individuals with a disorder of the corpus callosum (DCC) who volunteer to provide information and support to other families and individuals dealing with DCC .These resource families are not professionals, and they do not serve as representatives of the NODCC.

If you would like to be a volunteer Resource Family, please complete the form below.

Resource Family Consent Form

My signature gives permission to only share my name, email address, phone number, city and state, with other families in the NODCC Family Partnership Program. The gender and year of birth of person with a DCC will also be included if provided. I understand my participation is voluntary, and I may request my information provided below be removed from the NODCC Family Partnership Resource Family database at any time.

Type of DCC:
Is it okay to list information above?