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…
Coming from the Leukemia & Lymphoma Society, and before that the Chordoma Foundation, Breanna has established herself as a leader in the rare disease nonprofit fundraising…
CNF partners are invited to participate in the pilot program – to learn more about the Neurology Social Services Network, watch our video. LEXINGTON, KY…
While it might feel like a relief to finally have a referral for a child neurologist after what could have been a months-, or years-long,…
      CNF – CNS Joint Statement on the Invasion of Ukraine The Child Neurology Foundation envisions a world in which…
Your story matters. In 2022, CNF will convene its first-ever Patient Experience Bureau (PEB) consisting of parents, caregivers, and young adults to raise our shared…
Families living with neurological diagnoses show unbelievable courage and resilience each day. And since it’s our mission to provide them with the tools and resources…
Rare diseases are anything but rare to us. According to the National Institute of Health, 40% of rare disorders have a neurological component, and 90%…
From February 14 to 21, the Second Annual Seizure Action Plan Awareness Week will highlight the importance of having a seizure action plan in place. The…
Child Neurology Foundation CEO Amy Brin Appointed to National Institutes of Health Council Brin to serve on National Advisory Neurological Disorders and Stroke Council LEXINGTON,…
