2018 Child Neurology Foundation Neurodevelopmental Disabilities (NDD) Summer Research Scholarship Winner CNF proudly announces the winner of the 2018 scholarship: Ms. Brittany A. Charsar MD/PhD…
Don't Miss the 2018 PAME Conference! On June 14-16, 2018, the 4th Partners Against Mortality in Epilepsy (PAME) conference will again bring together health care providers, researchers,…
CNF Respite Care Notebook Goes International If your child lives with a special need, have you considered respite care? Developed with families, CNF created the Respite…
In partnership with UCB, a CNF 2018 Corporate Advisory Board Member, Mindspot Research is conducting online focus groups with Parents/Caregivers+ Adolescent Patients who have experienced childhood…
Join CNF as we connect with our neurology community at the 2018 American Academy of Neurology (AAN) Annual Meeting, April 21-27 in LA. Stop by CNF's…
“No journey is the same, but it is nice to know other people understand.”- Parent of a child with a neurologic condition who reached out…
Tools for Transitioning Young Adults with Neurologic Conditions Led by CNF, the consensus statement, The Neurologist’s Role in Supporting Transition to Adult Health Care* identified 8 Common Principles for…
Last month, CNF noted our commitment to children living with rare genetic conditions that have a neurologic component and introduced the RareChildNeuro 75% Fact... of…
Humans are more effective and happier when they have... someone to talk to about personal matters... someone who cares about them ... someone who can…
CNF is happy to share this opportunity from our Corporate Advisory Board Partner, Greenwich Bioscience Greenwich Biosciences is launching TakeOnEpilepsy.com to provide expert advice for…
What Does a Portrait of a Rare Caregiver Look Like? The National Alliance for Caregiving, in partnership with Global Genes, recently released Rare Disease Caregiving in America, a…
We want to change isolation to empowerment! The CNF/Global Genes Rare Child Neurology Workgroup wants to understand the needs of children living with rare genetic conditions that…
New Pilot Project Improving communication between pediatric neurologists and the families of children living with epilepsy “A majority of families wanted to discuss their child’s risk…
Parents/caregivers of 12 to 30-year olds living with a complex neurologic condition, let’s talk! CNF’s new Caregiver Perspectives on Transitions Project is interested in your experiences with different…
Please visit the January 30, 2018 O&A for more information. Don’t miss out on future Opportunities & Announcements from the child neurology community – subscribe…
Please visit the January 23, 2018 O&A for more information. Don’t miss out on future Opportunities & Announcements from the child neurology community – subscribe…
Please visit the January 18, 2018 O&A for more information. Don’t miss out on future Opportunities & Announcements from the child neurology community – subscribe…
Happy New Year from Child Neurology Foundation! Like many of you, we are jumping right into the new year — a time of excitement, new…
Tomorrow, December 1st, Kicks Off Infantile Spasms Awareness Week (ISAW) Identifying infantile spasms (IS) is critical for parents, caregivers, and providers. The earlier a…
“No journey is the same, but it’s nice to know other people understand.” “I came across your site and I would like for you…
