As COVID-19 vaccines are authorized and then recommended for use in the United States, information is changing rapidly. Here are a few things you need…
From our family at the Child Neurology Foundation to yours, we wish you a happy, healthy holiday season filled with good memories! Our offices are closed…
The June Jessee Memorial Foundation (JJMF) is a nonprofit organization that provides relief and support to help children with devastating medically complex, neurological conditions and…
We’d like to welcome Loren Wood to the CNF Team. To help you get to know him, Loren answered a few questions to share with…
Late in 2020, CNF was lucky enough to have two new members join our Board of Directors. One of those members is Timothy Engel, CPA,…
In late 2020, two new members joined the CNF Board of Directors. One of those members is Dr. Bruce Cohen, who is now President-Elect of…
Each year, we identify an important education initiative that impacts the entire child neurology community. In 2020, our focus was on Shortening the Diagnostic Odyssey, which included…
At CNF, we recognize the power of telehealth to improve access for so many children experiencing neurologic conditions and their families, and it provides another…
Congratulations to the 2020 PERF grants and NDD scholarship recipients! Every year, the Child Neurology Foundation — along with the Child Neurology Society and Pediatric…
Reuben has been an adventure from the get-go! He was likely having seizures before birth, but within the first few days of his birth shortly…
Update Oct. 26, 2020: The Child Neurology Foundation is pleased to announce that our facilitator Paul Cooper, CPF, alongside CEO Amy Brin, MSN, MA, PCNS-BC,…
We’d like to welcome Nicky Young to the CNF Team. To help you get to know her, Nicky answered a few questions to share with…
Check out our upcoming webinars about a variety of different topics here.
Our daughter May suffered what seemed like a small fall at the age of 5 months, she was rushed to the hospital after she threw…
“When we found out Lucas received a grant from the Child Neurology Foundation, it was almost as if it was an answered prayer. Lucas finally…
Luke really needed the social interaction, and since we started two weeks ago, the light is coming back into his eyes.
Mia is 3 years old and has a rare form of epilepsy, SCN8A, that causes developmental delays and other problems as well.
He has a smile that lights up a room, he loves people, and he’s also a typical rowdy boy.Â
Auggie is trained to alert to oncoming seizures, a job she takes very seriously. Auggie keeps our daughter safe, and affords her a level of…
We feel so blessed to have her in our lives. The joy that pours out of her is contagious.