In 2019, we saw an increase in conversations about SUDEP (Sudden Unexpected Death in Epilepsy) on mainstream media channels. Unfortunately, much of this attention was…
Part of CNF’s mission to build relationships and support community members who are dedicated to improving the lives of children living with neurological conditions, is supporting…
On September 17, the Child Neurology Foundation Team went to The Global Genes Patient Advocacy Summit in San Diego, California. As the largest gathering of…
Save the date! On December 5th in Baltimore, Maryland, CNF will be hosting our second annual Peer Support Best Practices Workshop (formerly Peer Support Bootcamp).…
Over the coming months, we’ll be sharing short interviews with the CNF staff, Board of Directors, and Corporate Advisory Board, with our community. In the…
Every year, CNF selects a promising medical student, with an interest in child neurology, to receive the Child Neurology Foundation Neurodevelopmental Disabilities Summer Scholarship. This…
On May 31st, 2019, the FDA held a public hearing, “to obtain scientific data and information about the safety, manufacturing, product quality, marketing, labeling, and sale of products…
In May of 2019, CNF staff attended the 71st American Academy of Neurology Annual Meeting (AANAM), which was held in Philadelphia. This is the biggest…
With great power comes great responsibility. Right? Or at least some clearly defined terms for how you work. As CNF grows, it’s been important to…
If you’ve visited CNF’s About Us page before, you’ve probably read our Mission and Vision Statements. Our Vision: A world in which all children affected by…