Welcome! This month CNF welcomed three new members to the board: Madeline Chadehumbe, MD Peter Kang, MD Monique Terrell Madeline Chadehumbe, MD Dr. Chadehumbe is…
Charlotte Martenz, 17 years old, experienced her first seizure at 4 months old and was diagnosed with Dravet syndrome in 2006 when she was nearly…
Did you know 1 in 5 children in the US live with a neurologic condition, many of which require life-long management of physical, cognitive, emotional,…
Since 2001, the Child Neurology Foundation has awarded over $4.1 million dollars in research funding and scholarships to young investigators and medical students in pursuit…
In honor of Child Neurology Awareness Day on Oct. 29, we are sharing stories from the Neuro Heroes in our community. Learn more about Child Neurology…
In honor of Child Neurology Awareness Day on Oct. 29, we are sharing stories from the Neuro Heroes in our community. Learn more about Child Neurology…
In honor of Child Neurology Awareness Day on Oct. 29, we are sharing stories from the Neuro Heroes in our community. Learn more about Child…
Reflections from Executive Director & CEO Amy Brin As we prepare for Child Neurology Awareness Day on Oct. 29, a day to celebrate the strength…
In honor of Child Neurology Awareness Day on Oct. 29, we are sharing stories from the Neuro Heroes in our community. Learn more about Child…
2023 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…
In honor of Child Neurology Awareness Day on Oct. 29, we are sharing stories from the Neuro Heroes in our community. Learn more about Child…
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…
LEXINGTON, KY., May 3, 2022— The Child Neurology Foundation (CNF) is pleased to be recognized by the Office of Disease Prevention and Health Promotion (ODPHP)…
How CNF’s Digital Access Program made a difference for the Torp family Access to technology is no longer a luxury. In this connected world, it’s…