1 in 5 children will live with a neurologic condition

We are here so they never have to walk alone!

At Child Neurology Foundation, we are committed to helping children and their families living with a neurologic condition receive the best quality of care — and achieve their highest quality of life — by providing information, education, and one-on-one support when it’s needed most.

Upcoming Webinars

When your newborn baby receives a neurologic diagnosis, it can feel overwhelming and frightening.

In our upcoming webinar, we discuss what neonatal neurology is and why getting a neurologic diagnosis for a newborn is important and we hear from a parent of a child who received a diagnosis in the NICU

Join us live on  July 29th at 1 p.m. ET with an opportunity to ask questions (you can also sign up to receive a copy of recording).

Newborn screening is a crucial test at birth that looks for genetic and metabolic conditions that can affect a child’s long-term health.

But what does the test look for? And what should you do if you receive an abnormal or out-of-range result?

Join us on August 4 at 2 p.m. ET to learn about newborn screening, what to expect, how early detection can help a child reach their full potential and tips for families that receive an early diagnosis.

Get Neurologic Condition Information

Child Neurologic Disorder Information & Resources

If your child or someone you know has recently been diagnosed with a neurologic condition, we’re here to help you make an informed decision on their care. Search our child neurology disorder directory to learn more about treatment, prognosis and research opportunities.

One-On-One Support

Not finding what you need? Would you like to talk with someone who has gone through a similar situation as you?

Timely Topics

Are you in search of a diagnosis?

The field of genetic testing is rapidly evolving and may be helpful in getting answers.

Struggling with bad behavior?

Discover techniques and tips to help you get your child’s behavior under control.

Are you having your doctors visits online now?

Learn how to make the most of your next virtual visit to the doctors office.

Thinking about your child’s transition to adulthood?

It is never too early to start planning and preparing for a child’s transition to adulthood.

What’s Happening Now

Getting to Know the CNF Team – Lindsey Taveren

We’d like to welcome Lindsey Taveren to the CNF Team! To help you get to…

Congratulations to our 2021 NDD Summer Research Scholarship Recipient!

Congratulations to Cole Deisseroth, recipient of CNF’s 2021 Neurodevelopmental Disabilities (NDD) Summer Research Scholarship!

Getting to know the CNF team – Loren Brigham

We’d like to welcome Loren Brigham to the CNF Team. To help you get to…

New Guide: Education Transition For Youth With Neurological Conditions

The Brain Recovery Project: Childhood Epilepsy Surgery Foundation has just launched a new step-by-step guide…

Our programming and family support services would not be possible without donations. Donate now to help us continue to provide critical support services for children and families in need.

Many Thanks to Our
Corporate Advisory Board Partners

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