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First annual Seizure Action Plan Awareness Week launches

This week (Feb. 8 -14) is the inaugural Seizure Action Plan Awareness Week, which is held annually starting on the second Monday in February in…

Audrey

Audrey goes to weekly therapy appointments and now we are doing full remote schooling for her. It hasn’t been easy being out of routine.

New Research Examines Why Child Neurologists Do, Or Do Not, Talk About SUDEP With Their Patients

Newly published research, funded in part by the Child Neurology Foundation, offers key insights about how and why child neurologists discuss SUDEP with their patients…

What you need to know: COVID-19 vaccine

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…

Happy holidays from our family to yours!

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…

June Jessee Memorial Foundation – Virtual Programming

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…

Getting to know the CNF team – Loren Wood

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…

Welcome to the Board – Timothy Engel

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,…

Welcome to the Board – Bruce Cohen

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…

Genetic Testing

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…

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