09/11/2026
As we look ahead to the rest of 2026, one of our biggest development priorities is also one of the simplest: helping more people know NODCC exists!
Awareness and fundraising are more connected than they may seem. Before someone becomes a donor, corporate partner, volunteer, or advocate, they first have to know who we are, understand why our work matters, and feel connected to the people we serve.
And that is where you can make an enormous difference.
You already have connections NODCC may never be able to reach through a mailing list or a cold email. Your employer may have a charitable giving program. A business you frequent may support local or national nonprofits. Your civic group, school, healthcare provider, professional association, or community foundation may be looking for organizations to support. Sometimes all it takes to open that door is someone saying, “I know an organization you should meet.”
Over the coming months, we’ll be working to increase awareness of Disorders of the Corpus Callosum while building relationships with individuals, foundations, businesses, and organizations that can help NODCC grow.
You can help right now by doing one simple thing: make a connection.
Introduce NODCC to someone in your network. Share an NODCC post. Tell your employer why this organization matters to your family. Ask whether your company offers matching gifts or community grants. Share your family's story. Invite someone new to learn about DCC.
You don't have to be a fundraiser to help NODCC fundraise.
You just have to help us open the next door.
Have a connection, idea, or potential partner we should know? We'd love to hear from you. Contact Naomi ([email protected]) and help us make sure more people discover NODCC! This helps more families discover a community where they belong.
Thank you!
