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$25,000 Goal
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Join Us for Our 2023 Fall Fundraiser!
Our 2023 Fall Fundraiser is in full swing, and we're calling on your support to help us achieve our goals!
The Fall Fundraiser marks the pinnacle of fundraising efforts for the National Organization for the Disorders of the Corpus Callosum (NODCC), all thanks to the incredible support we've received from families like yours over the years. In the past nine years, the dedication of individuals and families has resulted in over $136,600 in donations during our Fall Fundraiser, both online and offline! We invite you to become part of our team and make a difference. Our aspiration is to raise $25,000 in the 2023 Fall Fundraiser, and with our current membership of 6,000, imagine the impact if each member joined our cause!
Your generosity doesn't just fund vital programs that provide the latest information on disorders of the corpus callosum (DCC), including our website, educational videos, translations of ACC and Me books, and the Medical Outreach Program, but it also supports the upcoming 2024 NODCC conference in Chicago, Illinois. We rely on your generous contributions to make these initiatives possible.
The mission of the NODCC is to help raise awareness about disorders of the corpus callosum (DCC) and to encourage the scientific and medical communities to study its symptoms and causes.
Today, nearly 100,000 children & adults nationwide are living with these little known but prevalent neurological disorders, birth defects in which the brain structure that connects the two hemispheres of the brain is not formed properly or is absent altogether.
Children & adults diagnosed with corpus callosum disorders experience developmental delays and disabilities, language and speech impairments, and other neurological and behavioral problems. But those who are diagnosed early, and receive physical, occupational, and speech and language therapies, improve their chances of walking, talking, and one day living independently.
The NODCC operates on a very small budget, with the bulk of our activities carried out by parents, caregivers, educators, therapists, and doctors who volunteer their precious time in the effort to bring valuable information and resources to those living with a disorder of the corpus callosum.