Danielle’s Hope is a non-profit organization founded in 2010 in honor of Danielle Jones.
The organization is dedicated to providing needed resources and support to children in North Carolina suffering from rare diseases and their families. The organization provides financial assistance, connect families with available resources, and provide emotional support that will enhance the lives of affected children and their families.
We hope to raise awareness about rare diseases and how they impact children in our state, as well as build interest and support in our organization and its mission.
Danielle’s Hope provides necessary resources and support to children and family members in North Carolina affected by rare diseases.
That every child's medical needs are met
- That every child has the tools, technology, or devices necessary to thrive educationally and independently
- That all families receive the emotional support they need as caregivers of a child with a rare disease
Please feel free to contact us for additional information.