The 2025 SCN8A Annual Gathering, held in Atlanta, GA, was a powerful reminder of what makes this community so extraordinary. Families, clinicians, researchers, and industry…
Read ArticleBy Kacie CraigExecutive Director, The Cute Syndrome Foundation In May of this year, I had the honor of representing The Cute Syndrome Foundation at…
Read ArticleThe Cute Syndrome Foundation’s 10th Annual SCN8A Clinician, Researcher, and Family Gathering was a powerful and inspiring event, bringing together families, researchers, and clinicians…
Read ArticleAmidst the enchanting atmosphere of Orlando, Florida, The Cute Syndrome Foundation (TCSF) hosted its 9th Annual Clinician, Researcher, and Family Gathering from December 1st…
Read ArticleIn 2019, we all left Baltimore, Maryland thinking we’d hug each other once again in 2020, but we all know what happened next…COVID-19 destroyed…
Read ArticleEverything in 2020 felt different, didn’t it? This year The Cute Syndrome Foundation’s 6th Annual Clinician, Researcher, and Family Gathering was no exception…as we moved…
Read Article2020 has been quite a year. I know we are all disappointed about not being able to all be together in person for our…
Read ArticleWhen we heard about The Cute Syndrome Foundation’s Annual Gathering, I thought, oh, that would be so neat, but there’s no way we could make…
Read ArticleHelp us continue to support the SCN8A community through events like this Gathering. DONATE NOW A week ago today the SCN8A community started arriving…
Read ArticleOur SCN8A Annual Clinician, Researcher, and Family Gathering will be held in conjunction with the American Epilepsy Society Conference on December 6-7, 2019 at…
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