Gloria Rodriguez has spent nearly 10 years learning how to be the best advocate possible for her daughter Grace, a 9-year-old with Dravet Syndrome. Grace…
2022 Harnett Grant Thanks to the generous support of the Harnett Family, CNF is able to provide one $1,000 grant to a family with a…
Alyssa Kimball’s family of five has a lot on their plate.   Of the three children, ages 6 through 9, the youngest has autism plus a…
To continue to serve as a hub for the child neurology community, our organization regularly assesses the needs of our patients, caregivers, and neurologists. That’s why…
CNF is excited to open a community-wide call for nominations to its Board of Directors! We seek Board members who share CNF’s commitment to serve…
The Child Neurology Foundation (CNF) and the Child Neurology Society (CNS) work on behalf of children and families living with neurologic conditions within the United…
A Letter from Dr. Anup Patel, President of CNF Board of Directors, and Dr. Bruce Cohen, President of the Child Neurology Society The end…
Last month, CNF had the opportunity to speak with the White House Office of Science & Technology Policy (OSTP) about our Digital Access, Transitions of…
CEO Amy Brin on the difference, new AAP guidelines, and what families and doctors should know about palliative care In my years of experience working…
Pediatric development expert on what the new CDC milestones mean for you In February of 2022, the Centers for Disease Control (CDC) and American Academy…