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1 in 5 children will live with a neurologic condition

We are here so they never have to walk alone!

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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.

Program Spotlight: Digital Access

We launched our first Digital Access pilot program over the summer to provide families with the resources and support they need to have online access to telehealth, an online community, and digital educational resources.

We’re providing Google Chromebooks, WIFI “hotspots,” and a year’s worth of data to 100 families in Minnesota and Kentucky.

If you, or someone you know, can benefit from our Digital Access Program, please contact our programs team at programs@childneurologyfoundation.org to learn more about how we can help.

This pilot program is open to families in Minnesota or Kentucky that has at least one child with a neurologic condition, and lives in an underserved community.

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?

Contact Peer Support

Timely Topics

Are you in search of a diagnosis?

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

Learn More

Struggling with bad behavior?

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

Learn More

Are you having your doctors visits online now?

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

Learn More

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.

Learn More

What’s Happening Now

New Mission, New Board, Same Goal at Child Neurology Foundation
Posted on
by Clare
Posted in News

New Mission, New Board, Same Goal at Child Neurology Foundation

Future efforts expanded to support medical professionals, helping children and families living with a neurologic…

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New CNF Board of Directors Brings Incredible Professional Expertise and Lived Experiences
Posted on
by Clare
Posted in News

New CNF Board of Directors Brings Incredible Professional Expertise and Lived Experiences

It is with great excitement that we announce the Child Neurology Foundation’s 2021-2022 Board of…

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Updated CNF Mission Elevates Support for Medical Professionals  
Posted on
by Clare
Posted in News

Updated CNF Mission Elevates Support for Medical Professionals  

Our 20th anniversary this year brings an exciting update to our mission and an added focus on supporting medical professionals as we seek to help children and families get the best…

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A Front Row Seat To A Medical Breakthrough In Pediatric Neurology: One Mother’s Journey
Posted on
by Clare
Posted in InsightsNo Category

A Front Row Seat To A Medical Breakthrough In Pediatric Neurology: One Mother’s Journey

Maria Kefalas, mother of Cal and author of ” Harnessing Grief: One Mother’s Quest for…

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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.

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Many Thanks to Our
Corporate Advisory Board Partners

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