A selection of stories from families in our community during the pandemic.
It is critical to get to a diagnosis sooner so that parents, caregivers, and physicians can begin the process of finding possible treatments and make…
The Child Neurology Foundation is pleased to announce that CEO and Executive Director Amy Brin is furthering her commitment to the pediatric neurology community and…
We’d like to welcome Greta Pittard to the CNF Team. To help you get to know her, Greta answered a few questions to share with…
In 2020, we’re making some additions to the CNF team to help us better serve the child neurology community. Please join us in welcoming Clare…
Whenever we bring on new staff at CNF, we like to introduce them to our community. Meet Jessica Nickrand, who joined the CNF team in…
CHICA is a web-based clinical decision support system that works with a physician’s current Electronic Health Record System to help coordinate patient visits.
In addition to offering support and guidance to our community in the time of COVID-19, we also want to share an update of how CNF…
In recent months, SARS2-CoV-2, a new form of a class of viruses referred to as Coronavirus has caused an illness known as COVID-19. COVID-19 has…
Every year, the Child Neurology Foundation’s (CNF) Board of Directors identifies an important Education Initiative that impacts the entire child neurology community. In 2020, this…
In a recent blog post, we talked about the importance of having conversations about SUDEP, and shared some resources to help facilitate this conversation. In…
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…
In late 2019, two new members joined the CNF Board of Directors. One of those members is Donald Pearl. This membership marks a momentous occasion,…
Late in 2019, CNF was lucky enough to have two new members join our Board of Directors. You may know him from twitter, as @TheNotoriousEEG,…
Welcome back to our weekly interview series! Each week, we share an interview with a member of the CNF community. Today, we’re highlighting the work…
Each week, we’re sharing profiles on the amazing people who make our mission in action possible. This week, we’re highlighting Paul Cooper, CNF’s facilitator. What’s…
Every week, we’re profiling members of the CNF community so you can get to know the people behind our organization’s mission. Meet Sue Yudovin, a…
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…
Each week, we’re sharing a profile from a member of the CNF team. This week, meet Cyndi Wright, who manages CNF’s Strategic Operations.  What’s your…
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…