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Getting to Know the CNF Team – Anup Patel, MD

Welcome back to our weekly interview series! Each week, we share an interview with a member of the CNF community. Today, we’re highlighting the work…

Getting to know the CNF team – Paul Cooper

Each week, we’re sharing profiles on the amazing people who make our mission in action possible. This week, we’re highlighting Paul Cooper, CNF’s facilitator. What’s…

Getting to know the CNF team – Sue Yudovin

Every week, we’re profiling members of the CNF community so you can get to know the people behind our organization’s mission. Meet Sue Yudovin, a…

2019 Scholarship Winners

Part of CNF’s mission to build relationships and support community members who are dedicated to improving the lives of children living with neurological conditions, is supporting…

Getting to know the CNF team – Cyndi Wright

Each week, we’re sharing a profile from a member of the CNF team. This week, meet Cyndi Wright, who manages CNF’s Strategic Operations.   What’s your…

Global Genes Patient Advocacy Summit Recap

On September 17, the Child Neurology Foundation Team went to The Global Genes Patient Advocacy Summit in San Diego, California. As the largest gathering of…

Getting to know the CNF team – Phillip Pearl, MD

Every week, we’re sharing an interview with the a member of the CNF community, starting with our staff, Board of Directors. This week, get to…

Getting to Know the CNF Team – Katherine Barnhart

Meet Katherine Barnhart. What’s your role at CNF? Executive Assistant to Amy Brin, Executive Director/CEO of CNF How do you spend your time when you’re…

2019 Peer Support Best Practices Workshop

Save the date! On December 5th in Baltimore, Maryland, CNF will be hosting our second annual Peer Support Best Practices Workshop (formerly Peer Support Bootcamp).…

Getting to know the CNF Team – Stephen M. Peters

This week on the blog, we’re getting to know one of the members of our Board of Directors. Meet Stephen Peters. Tell us what you…

Getting to know the CNF Team – Katie Hentges

Each week, on the CNF blog, we’re sharing a post about a member of the CNF community; starting with our Staff, Board of Directors, and…

Getting to know the CNF Team – Amy Brin

Over the coming months, we’ll be sharing short interviews with the CNF staff, Board of Directors, and Corporate Advisory Board, with our community. In the…

2019 Child Neurology Foundation Neurodevelopmental Disabilities Summer Scholarship Winner

Every year, CNF selects a promising medical student, with an interest in child neurology, to receive the Child Neurology Foundation Neurodevelopmental Disabilities Summer Scholarship. This…

CNF’s Statement on the FDA’s May 31st CBD Hearing

On May 31st, 2019, the FDA held a public hearing, “to obtain scientific data and information about the safety, manufacturing, product quality, marketing, labeling, and sale of products…

CNF at the 2019 AANAM

In May of 2019, CNF staff attended the 71st American Academy of Neurology Annual Meeting (AANAM), which was held in Philadelphia. This is the biggest…

New Policies to Guide CNF Engagement

With great power comes great responsibility. Right? Or at least some clearly defined terms for how you work. As CNF grows, it’s been important to…

CNF Core Values

If you’ve visited CNF’s About Us page before, you’ve probably read our Mission and Vision Statements. Our Vision: A world in which all children affected by…

See you an AAN!

CNF staff is busy getting ready for the upcoming American Academy of Neurology Annual Meeting held May 4th to 11th in Philadelphia. CNF is in…

1:26 The Art of Epilepsy 2019: Call to Artists

2019 Call for Artists This fall, CNF and the Child Neurology Society  are partnering with the Hidden Truths Project for 1:26 the Art of Epilepsy…

IT startup launches software to encourage physician-family conversations about epilepsy

NEWS RELEASE INDIANAPOLIS — Physicians can now be alerted to pediatric patients’ risk of sudden unexpected death in epilepsy, or SUDEP, during routine primary care…

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