Join us June 15th-24th for the inaugural 2021 Transitions of Care Summit
All parents have questions and concerns about sending their children back to school during the current pandemic, but the child neurology community faces additional challenges.
We explore the existing chasm between healthcare providers’ ability to offer behavior management support guidance and families’ desires to have access to the best treatment available for their children.
The Child Neurology Foundation is launching a new project Better Together for Kids that kicks off this March, exploring how we can support better collaboration and connection between advocacy and industry in our sector.
We encourage you to fill out the Child Neurologist New Visit Toolkit prior to your first visit with a neurologist or when visiting a new neurologist. Download the form, print it out and bring it to the…
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.
Where there is research for the advancement of treatments and cures, there are accompanying clinical trials. All clinical trials listed on this page are registered with clinicaltrials.gov.
Navigating the New Normal – Resources, educational content, stories and grants for coping with COVID-19
We’re launching a pilot project to provide digital access to 100 families in our child neuro community who don’t have internet at home. The goal? Help them get online and access to the resources and…
A list of diseases and conditions sourced through CNF’s partnership with The National Institute of Neurological Disorders and Stroke (NINDS), US National Institutes of Health.
Although epilepsy cannot be cured, many people control seizures with medication, lifestyle changes, devices, and/or surgery. It is important to control seizures as much as possible to reduce the risk of injury, health complications and,…
The application portal is now closed and selected sites will be notified. As part of our effort to elevate the importance of genetic testing, and the role it can play in shortening the diagnostic journey…
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 genetic testing and the role it can play in helping…
CNF offers Grants & Scholarships every year to families in our child neurology community, including the RISE Family grants to help during COVID-19.
Infantile spasms are a rare, but very serious type of seizure.
You are not alone. Millions of people face mental health concerns every year; the latest data from the National Alliance on Mental Health shows that one in five U.S. adults experience mental illness and 17…
Peer support is a form of emotional and practical help from somebody who has lived through a similar experience and who is trained to offer support.
Use the forms in this free Notebook to tell the respite caregivers about your child and his/her needs.
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 more informed decisions about next steps in the care of…
Every year, 1 in 150 people who have uncontrolled seizures dies from Sudden Unexpected Death in Epilepsy (SUDEP). It is the leading epilepsy-related cause of death.
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 way to stay safe as we navigate our new normal.
Our largest and most diverse program helps to support youth, families, and child neurology teams in the medical transition from pediatric to adult health care systems.
Check out our upcoming webinars about a variety of different topics here.
CNF’s Community of Practice gathering is a way to provide a safe forum for people in our sector to support one another, connecting about our hopes, anxieties, dilemmas, and successes.
Infantile spasms are a rare, but very serious type of seizure.
A list of diseases and conditions sourced through CNF’s partnership with The National Institute of Neurological Disorders and Stroke (NINDS), US National Institutes of Health.
Navigating the New Normal – Resources, educational content, stories and grants for coping with COVID-19
CNF is passionate about collaboration. Here is a list of opportunities for organizations to partner with us.
CNF offers Grants & Scholarships every year to health care providers and researchers in our child neurology community.
We explore the existing chasm between healthcare providers’ ability to offer behavior management support guidance and families’ desires to have access to the best treatment available for their children.
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.
Use the forms in this free Notebook to tell the respite caregivers about your child and his/her needs.
Peer support is a form of emotional and practical help from somebody who has lived through a similar experience and who is trained to offer support.
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 more informed decisions about next steps in the care of…
Every year, 1 in 150 people who have uncontrolled seizures dies from Sudden Unexpected Death in Epilepsy (SUDEP). It is the leading epilepsy-related cause of death.
Our largest and most diverse program helps to support youth, families, and child neurology teams in the medical transition from pediatric to adult health care systems.
Where there is research for the advancement of treatments and cures, there are accompanying clinical trials. All clinical trials listed on this page are registered with clinicaltrials.gov.
All parents have questions and concerns about sending their children back to school during the current pandemic, but the child neurology community faces additional challenges.
Check out our upcoming webinars about a variety of different topics here.
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 way to stay safe as we navigate our new normal.
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 genetic testing and the role it can play in helping…
The application portal is now closed and selected sites will be notified. As part of our effort to elevate the importance of genetic testing, and the role it can play in shortening the diagnostic journey…
Although epilepsy cannot be cured, many people control seizures with medication, lifestyle changes, devices, and/or surgery. It is important to control seizures as much as possible to reduce the risk of injury, health complications and,…
Although epilepsy cannot be cured, many people control seizures with medication, lifestyle changes, devices, and/or surgery. It is important to control seizures as much as possible to reduce the risk of injury, health complications and,…
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 way to stay safe as we navigate our new normal.
CNF offers Grants & Scholarships every year to families in our child neurology community, including the RISE Family grants to help during COVID-19.
Check out our upcoming webinars about a variety of different topics here.
Peer support is a form of emotional and practical help from somebody who has lived through a similar experience and who is trained to offer support.
We explore the existing chasm between healthcare providers’ ability to offer behavior management support guidance and families’ desires to have access to the best treatment available for their children.
Infantile spasms are a rare, but very serious type of seizure.
Where there is research for the advancement of treatments and cures, there are accompanying clinical trials. All clinical trials listed on this page are registered with clinicaltrials.gov.
All parents have questions and concerns about sending their children back to school during the current pandemic, but the child neurology community faces additional challenges.
The Child Neurology Foundation is launching a new project Better Together for Kids that kicks off this March, exploring how we can support better collaboration and connection between advocacy and industry in our sector.
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.
Use the forms in this free Notebook to tell the respite caregivers about your child and his/her needs.
A list of diseases and conditions sourced through CNF’s partnership with The National Institute of Neurological Disorders and Stroke (NINDS), US National Institutes of Health.
CNF’s Community of Practice gathering is a way to provide a safe forum for people in our sector to support one another, connecting about our hopes, anxieties, dilemmas, and successes.
Every year, 1 in 150 people who have uncontrolled seizures dies from Sudden Unexpected Death in Epilepsy (SUDEP). It is the leading epilepsy-related cause of death.
Navigating the New Normal – Resources, educational content, stories and grants for coping with COVID-19
CNF offers Grants & Scholarships every year to health care providers and researchers in our child neurology community.
CNF is passionate about collaboration. Here is a list of opportunities for organizations to partner with us.
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 genetic testing and the role it can play in helping…
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 more informed decisions about next steps in the care of…
Where there is research for the advancement of treatments and cures, there are accompanying clinical trials. All clinical trials listed on this page are registered with clinicaltrials.gov.
The Child Neurology Foundation is launching a new project Better Together for Kids that kicks off this March, exploring how we can support better collaboration and connection between advocacy and industry in our sector.
CNF is passionate about collaboration. Here is a list of opportunities for organizations to partner with us.
CNF’s Community of Practice gathering is a way to provide a safe forum for people in our sector to support one another, connecting about our hopes, anxieties, dilemmas, and successes.
Navigating the New Normal – Resources, educational content, stories and grants for coping with COVID-19
A list of diseases and conditions sourced through CNF’s partnership with The National Institute of Neurological Disorders and Stroke (NINDS), US National Institutes of Health.
Your gift improves the lives of children and families living with neurologic conditions, by supporting CNF’s vision of a world where children and their families living with neurologic conditions reach their full potential.
All parents have questions and concerns about sending their children back to school during the current pandemic, but the child neurology community faces additional challenges.
CNF offers Grants & Scholarships every year to health care providers and researchers in our child neurology community.
In addition to financial support, members provide their unique expertise and perspectives on the issues and needs facing the child neurology community.
CNF offers Grants & Scholarships every year to families in our child neurology community, including the RISE Family grants to help during COVID-19.
Join us June 15th-24th for the inaugural 2021 Transitions of Care Summit
All parents have questions and concerns about sending their children back to school during the current pandemic, but the child neurology community faces additional challenges.
We explore the existing chasm between healthcare providers’ ability to offer behavior management support guidance and families’ desires to have access to the best treatment available for their children.
The Child Neurology Foundation is launching a new project Better Together for Kids that kicks off this March, exploring how we can support better collaboration and connection between advocacy and industry in our sector.
We encourage you to fill out the Child Neurologist New Visit Toolkit prior to your first visit with a neurologist or when visiting a new neurologist. Download the form, print it out and bring it to the…
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.
Where there is research for the advancement of treatments and cures, there are accompanying clinical trials. All clinical trials listed on this page are registered with clinicaltrials.gov.
Navigating the New Normal – Resources, educational content, stories and grants for coping with COVID-19
We’re launching a pilot project to provide digital access to 100 families in our child neuro community who don’t have internet at home. The goal? Help them get online and access to the resources and…
A list of diseases and conditions sourced through CNF’s partnership with The National Institute of Neurological Disorders and Stroke (NINDS), US National Institutes of Health.
Although epilepsy cannot be cured, many people control seizures with medication, lifestyle changes, devices, and/or surgery. It is important to control seizures as much as possible to reduce the risk of injury, health complications and,…
The application portal is now closed and selected sites will be notified. As part of our effort to elevate the importance of genetic testing, and the role it can play in shortening the diagnostic journey…
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 genetic testing and the role it can play in helping…
CNF offers Grants & Scholarships every year to families in our child neurology community, including the RISE Family grants to help during COVID-19.
Infantile spasms are a rare, but very serious type of seizure.
You are not alone. Millions of people face mental health concerns every year; the latest data from the National Alliance on Mental Health shows that one in five U.S. adults experience mental illness and 17…
Peer support is a form of emotional and practical help from somebody who has lived through a similar experience and who is trained to offer support.
Use the forms in this free Notebook to tell the respite caregivers about your child and his/her needs.
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 more informed decisions about next steps in the care of…
Every year, 1 in 150 people who have uncontrolled seizures dies from Sudden Unexpected Death in Epilepsy (SUDEP). It is the leading epilepsy-related cause of death.
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 way to stay safe as we navigate our new normal.
Our largest and most diverse program helps to support youth, families, and child neurology teams in the medical transition from pediatric to adult health care systems.
Check out our upcoming webinars about a variety of different topics here.
Although epilepsy cannot be cured, many people control seizures with medication, lifestyle changes, devices, and/or surgery. It is important to control seizures as much as possible to reduce the risk of injury, health complications and,…
The application portal is now closed and selected sites will be notified. As part of our effort to elevate the importance of genetic testing, and the role it can play in shortening the diagnostic journey…
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 genetic testing and the role it can play in helping…
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 way to stay safe as we navigate our new normal.
Check out our upcoming webinars about a variety of different topics here.
CNF’s Community of Practice gathering is a way to provide a safe forum for people in our sector to support one another, connecting about our hopes, anxieties, dilemmas, and successes.
A list of diseases and conditions sourced through CNF’s partnership with The National Institute of Neurological Disorders and Stroke (NINDS), US National Institutes of Health.
Navigating the New Normal – Resources, educational content, stories and grants for coping with COVID-19
All parents have questions and concerns about sending their children back to school during the current pandemic, but the child neurology community faces additional challenges.
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 more informed decisions about next steps in the care of…
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.
CNF is passionate about collaboration. Here is a list of opportunities for organizations to partner with us.
We explore the existing chasm between healthcare providers’ ability to offer behavior management support guidance and families’ desires to have access to the best treatment available for their children.
Our largest and most diverse program helps to support youth, families, and child neurology teams in the medical transition from pediatric to adult health care systems.
Peer support is a form of emotional and practical help from somebody who has lived through a similar experience and who is trained to offer support.
Every year, 1 in 150 people who have uncontrolled seizures dies from Sudden Unexpected Death in Epilepsy (SUDEP). It is the leading epilepsy-related cause of death.
Use the forms in this free Notebook to tell the respite caregivers about your child and his/her needs.
Infantile spasms are a rare, but very serious type of seizure.
Where there is research for the advancement of treatments and cures, there are accompanying clinical trials. All clinical trials listed on this page are registered with clinicaltrials.gov.
CNF offers Grants & Scholarships every year to health care providers and researchers in our child neurology community.
Although epilepsy cannot be cured, many people control seizures with medication, lifestyle changes, devices, and/or surgery. It is important to control seizures as much as possible to reduce the risk of injury, health complications and,…
The Child Neurology Foundation is launching a new project Better Together for Kids that kicks off this March, exploring how we can support better collaboration and connection between advocacy and industry in our sector.
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 genetic testing and the role it can play in helping…
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 way to stay safe as we navigate our new normal.
Check out our upcoming webinars about a variety of different topics here.
CNF’s Community of Practice gathering is a way to provide a safe forum for people in our sector to support one another, connecting about our hopes, anxieties, dilemmas, and successes.
A list of diseases and conditions sourced through CNF’s partnership with The National Institute of Neurological Disorders and Stroke (NINDS), US National Institutes of Health.
Navigating the New Normal – Resources, educational content, stories and grants for coping with COVID-19
All parents have questions and concerns about sending their children back to school during the current pandemic, but the child neurology community faces additional challenges.
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 more informed decisions about next steps in the care of…
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.
CNF is passionate about collaboration. Here is a list of opportunities for organizations to partner with us.
We explore the existing chasm between healthcare providers’ ability to offer behavior management support guidance and families’ desires to have access to the best treatment available for their children.
Peer support is a form of emotional and practical help from somebody who has lived through a similar experience and who is trained to offer support.
Every year, 1 in 150 people who have uncontrolled seizures dies from Sudden Unexpected Death in Epilepsy (SUDEP). It is the leading epilepsy-related cause of death.
CNF offers Grants & Scholarships every year to families in our child neurology community, including the RISE Family grants to help during COVID-19.
Use the forms in this free Notebook to tell the respite caregivers about your child and his/her needs.
Infantile spasms are a rare, but very serious type of seizure.
Where there is research for the advancement of treatments and cures, there are accompanying clinical trials. All clinical trials listed on this page are registered with clinicaltrials.gov.
CNF offers Grants & Scholarships every year to health care providers and researchers in our child neurology community.
The Child Neurology Foundation is launching a new project Better Together for Kids that kicks off this March, exploring how we can support better collaboration and connection between advocacy and industry in our sector.
CNF’s Community of Practice gathering is a way to provide a safe forum for people in our sector to support one another, connecting about our hopes, anxieties, dilemmas, and successes.
A list of diseases and conditions sourced through CNF’s partnership with The National Institute of Neurological Disorders and Stroke (NINDS), US National Institutes of Health.
Navigating the New Normal – Resources, educational content, stories and grants for coping with COVID-19
All parents have questions and concerns about sending their children back to school during the current pandemic, but the child neurology community faces additional challenges.
CNF is passionate about collaboration. Here is a list of opportunities for organizations to partner with us.
CNF offers Grants & Scholarships every year to families in our child neurology community, including the RISE Family grants to help during COVID-19.
Your gift improves the lives of children and families living with neurologic conditions, by supporting CNF’s vision of a world where children and their families living with neurologic conditions reach their full potential.
In addition to financial support, members provide their unique expertise and perspectives on the issues and needs facing the child neurology community.
Where there is research for the advancement of treatments and cures, there are accompanying clinical trials. All clinical trials listed on this page are registered with clinicaltrials.gov.
CNF offers Grants & Scholarships every year to health care providers and researchers in our child neurology community.