Grappling with my daughter’s epilepsy diagnosis
Madeleine Oudin's daughter Margot was found to have SCN8A mutation causing epilepsy. Here she tells her story as both a scientist and mother.
SCN8A – the needle in the haystack
As part of our Patient Advocacy and Engagement program, we welcome guest blogger Ben Clay, whose daughter Tilly was diagnosed with SCN8A when she was 8.