We are thrilled to announce that we have partnered with CNF to better serve our pediatric community of MOGAD patients!
Parents and caregivers of chidren with MOGAD can now visit the CNF website and learn about MOGAD through their Child Neurology Foundation’s MOG Antibody Disease Information Page.
The Child Neurology Foundation is a nonprofit patient advocacy organization. CNF’s mission is to serve as a collaborative center of education, resources, and support for children with neurologic conditions and their families. CNF also helps facilitate connections with medical professionals who care for them. According to their website, 1 in 5 children will live with a neurologic condition. While rare, some of those children will have MOG Antibody Disease. With our partnership, those families who are diagnosed with MOGAD will be able to have the power of both of our organizations behind them, with valuable resources for advice on IEP/504 advice and assistance as well as great resources to help find medical professionals.
We look to CNF to help us expand our resources and aid for patients and they will look to us to help those who contact them from the MOGAD Community. A perfect partnership and better help and advocacy for patients and caregivers of children with this difficult and life-changing disease.
